Run ID: ERR4818929
Sample name:
Date: 01-04-2023 15:50:06
Number of reads: 853291
Percentage reads mapped: 21.46
Strain:
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| katG | 2155693 | p.Ser140Asn | missense_variant | 1.0 | isoniazid |
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| embB | 4247588 | p.Leu359Ile | missense_variant | 1.0 | ethambutol |
| embB | 4247708 | p.Asn399Asp | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
| gyrB | 6097 | c.858G>A | synonymous_variant | 1.0 |
| gyrB | 6103 | c.864G>A | synonymous_variant | 0.57 |
| gyrB | 6104 | p.Ile289Val | missense_variant | 0.4 |
| gyrB | 6109 | c.870G>C | synonymous_variant | 0.46 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6122 | p.Ala295Gln | missense_variant | 0.5 |
| gyrB | 6127 | c.888G>A | synonymous_variant | 0.41 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 0.5 |
| gyrB | 6171 | p.His311Arg | missense_variant | 0.46 |
| gyrB | 6184 | c.945C>T | synonymous_variant | 0.54 |
| gyrB | 6209 | c.970C>T | synonymous_variant | 0.64 |
| gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
| gyrB | 6215 | p.Ser326Thr | missense_variant | 0.62 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6250 | c.1011A>C | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6256 | c.1017G>A | synonymous_variant | 1.0 |
| gyrB | 6265 | c.1026C>T | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 6355 | c.-947G>A | upstream_gene_variant | 1.0 |
| gyrA | 6370 | c.-932C>T | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 1.0 |
| gyrA | 6400 | c.-902C>G | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 1.0 |
| gyrA | 6418 | c.-884C>G | upstream_gene_variant | 1.0 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 1.0 |
| gyrA | 6430 | c.-872A>G | upstream_gene_variant | 1.0 |
| gyrB | 6440 | p.Thr401Ala | missense_variant | 1.0 |
| gyrA | 6448 | c.-854G>C | upstream_gene_variant | 1.0 |
| gyrA | 6460 | c.-842G>C | upstream_gene_variant | 1.0 |
| gyrA | 6469 | c.-833T>G | upstream_gene_variant | 1.0 |
| gyrA | 6472 | c.-830G>C | upstream_gene_variant | 1.0 |
| gyrA | 6475 | c.-827C>G | upstream_gene_variant | 0.94 |
| gyrA | 6490 | c.-812T>C | upstream_gene_variant | 1.0 |
| gyrA | 6499 | c.-803A>G | upstream_gene_variant | 1.0 |
| gyrA | 6508 | c.-794A>G | upstream_gene_variant | 1.0 |
| gyrA | 6511 | c.-791A>G | upstream_gene_variant | 1.0 |
| gyrA | 6526 | c.-776T>C | upstream_gene_variant | 1.0 |
| gyrA | 6535 | c.-767C>G | upstream_gene_variant | 1.0 |
| gyrB | 6542 | p.Ile435Leu | missense_variant | 1.0 |
| gyrA | 6550 | c.-752A>G | upstream_gene_variant | 1.0 |
| gyrA | 6551 | c.-751T>C | upstream_gene_variant | 1.0 |
| gyrA | 6577 | c.-725T>C | upstream_gene_variant | 1.0 |
| gyrA | 6580 | c.-722C>G | upstream_gene_variant | 1.0 |
| gyrA | 6583 | c.-719G>C | upstream_gene_variant | 1.0 |
| gyrA | 6589 | c.-713G>C | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6625 | c.-677G>T | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>C | upstream_gene_variant | 1.0 |
| gyrA | 6649 | c.-653T>C | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6706 | c.-596G>A | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6724 | c.-578G>C | upstream_gene_variant | 1.0 |
| gyrA | 6727 | c.-575G>C | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrA | 6733 | c.-569G>A | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.57 |
| gyrA | 6748 | c.-554G>A | upstream_gene_variant | 0.43 |
| gyrB | 6749 | p.Ala504Ser | missense_variant | 0.57 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.52 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6787 | c.-515G>A | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 0.97 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6866 | c.-436C>T | upstream_gene_variant | 0.54 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>C | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421T>C | upstream_gene_variant | 1.0 |
| gyrA | 6898 | c.-404G>C | upstream_gene_variant | 1.0 |
| gyrA | 6904 | c.-398C>G | upstream_gene_variant | 1.0 |
| gyrA | 6910 | c.-392G>A | upstream_gene_variant | 1.0 |
| gyrB | 6911 | p.Asn558His | missense_variant | 1.0 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>C | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
| gyrA | 6955 | c.-347G>A | upstream_gene_variant | 1.0 |
| gyrA | 6961 | c.-341G>A | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrB | 6970 | p.Asp577Glu | missense_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 6985 | c.-317C>T | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>C | upstream_gene_variant | 1.0 |
| gyrA | 7012 | c.-290G>C | upstream_gene_variant | 1.0 |
| gyrB | 7015 | p.Glu592Asp | missense_variant | 1.0 |
| gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
| gyrA | 7021 | c.-281G>C | upstream_gene_variant | 1.0 |
| gyrA | 7027 | c.-275G>A | upstream_gene_variant | 1.0 |
| gyrB | 7028 | p.Ala597Ser | missense_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrA | 7048 | c.-254G>A | upstream_gene_variant | 1.0 |
| gyrA | 7051 | c.-251A>G | upstream_gene_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7100 | c.-202T>C | upstream_gene_variant | 1.0 |
| gyrA | 7108 | c.-194G>A | upstream_gene_variant | 1.0 |
| gyrA | 7114 | c.-188C>G | upstream_gene_variant | 1.0 |
| gyrA | 7120 | c.-182T>C | upstream_gene_variant | 1.0 |
| gyrA | 7129 | c.-173T>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7147 | c.-155G>C | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>C | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7177 | c.-125G>A | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7192 | c.-110G>C | upstream_gene_variant | 1.0 |
| gyrA | 7198 | c.-104C>T | upstream_gene_variant | 0.75 |
| gyrA | 7201 | c.-101G>A | upstream_gene_variant | 0.75 |
| gyrA | 7213 | c.-89G>C | upstream_gene_variant | 0.75 |
| gyrA | 7216 | c.-86G>C | upstream_gene_variant | 0.75 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 0.75 |
| gyrA | 7243 | c.-59G>A | upstream_gene_variant | 0.75 |
| gyrA | 7343 | c.42G>C | synonymous_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7418 | c.117C>G | synonymous_variant | 1.0 |
| gyrA | 7424 | c.123G>A | synonymous_variant | 1.0 |
| gyrA | 7430 | c.129G>A | synonymous_variant | 1.0 |
| gyrA | 7436 | c.135C>T | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>A | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
| gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
| gyrA | 7463 | c.162G>C | synonymous_variant | 1.0 |
| gyrA | 7469 | c.168C>G | synonymous_variant | 1.0 |
| gyrA | 7496 | c.195C>G | synonymous_variant | 1.0 |
| gyrA | 7514 | c.213C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>C | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7550 | c.249C>T | synonymous_variant | 1.0 |
| gyrA | 7565 | c.264C>T | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7587 | c.286C>T | synonymous_variant | 0.97 |
| gyrA | 7601 | c.300C>G | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 1.0 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7670 | c.369A>G | synonymous_variant | 1.0 |
| gyrA | 7679 | c.378G>C | synonymous_variant | 1.0 |
| gyrA | 7683 | c.382A>C | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7703 | c.402G>C | synonymous_variant | 1.0 |
| gyrA | 7721 | c.420G>A | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7748 | c.447A>G | synonymous_variant | 1.0 |
| gyrA | 7763 | c.462T>G | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7787 | c.486G>A | synonymous_variant | 1.0 |
| gyrA | 7793 | c.492G>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7806 | c.505C>A | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7889 | c.588G>A | synonymous_variant | 1.0 |
| gyrA | 8054 | c.753T>C | synonymous_variant | 1.0 |
| gyrA | 8057 | c.756A>G | synonymous_variant | 1.0 |
| gyrA | 8066 | c.765A>G | synonymous_variant | 1.0 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 1.0 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>G | synonymous_variant | 1.0 |
| gyrA | 8093 | c.792C>A | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>C | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8105 | c.804G>T | synonymous_variant | 1.0 |
| gyrA | 8106 | c.805C>T | synonymous_variant | 1.0 |
| gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8174 | c.873C>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>T | synonymous_variant | 1.0 |
| gyrA | 8184 | p.Lys295Arg | missense_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 1.0 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 1.0 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8258 | c.957G>A | synonymous_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8279 | c.978G>C | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8315 | c.1014G>A | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>C | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8360 | c.1059G>C | synonymous_variant | 1.0 |
| gyrA | 8372 | c.1071G>C | synonymous_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
| gyrA | 8393 | c.1092T>C | synonymous_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8401 | p.Asp367Ala | missense_variant | 1.0 |
| gyrA | 8408 | c.1107A>G | synonymous_variant | 1.0 |
| gyrA | 8411 | c.1110C>T | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8423 | c.1122G>C | synonymous_variant | 1.0 |
| gyrA | 8447 | c.1146C>G | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>C | synonymous_variant | 1.0 |
| gyrA | 8465 | c.1164C>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8472 | c.1171C>T | synonymous_variant | 1.0 |
| gyrA | 8480 | c.1179C>T | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8492 | c.1191G>C | synonymous_variant | 1.0 |
| gyrA | 8501 | c.1200G>C | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>G | synonymous_variant | 1.0 |
| gyrA | 8520 | c.1219C>T | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8555 | c.1254G>C | synonymous_variant | 1.0 |
| gyrA | 8556 | p.Ala419Thr | missense_variant | 1.0 |
| gyrA | 8561 | c.1260A>C | synonymous_variant | 1.0 |
| gyrA | 8571 | c.1270C>T | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
| gyrA | 8606 | c.1305C>T | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 1.0 |
| gyrA | 8633 | c.1332C>G | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>G | synonymous_variant | 1.0 |
| gyrA | 8637 | c.1336C>T | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8645 | c.1344C>G | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8696 | c.1395G>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8731 | p.Gly477Ala | missense_variant | 1.0 |
| gyrA | 8738 | c.1437G>C | synonymous_variant | 1.0 |
| gyrA | 8747 | c.1446A>G | synonymous_variant | 1.0 |
| gyrA | 8756 | c.1455A>G | synonymous_variant | 1.0 |
| gyrA | 8761 | p.Val487Ala | missense_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8792 | c.1491G>C | synonymous_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8813 | p.Asp504Glu | missense_variant | 1.0 |
| gyrA | 8818 | p.Ser506Asn | missense_variant | 1.0 |
| gyrA | 8828 | c.1527T>C | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528_1530delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8966 | c.1665C>G | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Arg | missense_variant | 1.0 |
| gyrA | 8981 | c.1680G>C | synonymous_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>G | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9038 | c.1737C>G | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>G | synonymous_variant | 1.0 |
| gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9074 | c.1773G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9092 | c.1791C>G | synonymous_variant | 1.0 |
| gyrA | 9164 | c.1863G>C | synonymous_variant | 1.0 |
| gyrA | 9167 | c.1866C>T | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9197 | c.1896G>C | synonymous_variant | 0.97 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 0.97 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 0.97 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 0.97 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 0.97 |
| gyrA | 9251 | c.1950G>T | synonymous_variant | 0.97 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 0.97 |
| gyrA | 9268 | p.Asn656Thr | missense_variant | 0.92 |
| gyrA | 9276 | c.1975C>T | synonymous_variant | 0.9 |
| gyrA | 9281 | c.1980C>G | synonymous_variant | 0.89 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 0.86 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 0.88 |
| gyrA | 9299 | c.1998_1999insTC | frameshift_variant | 0.86 |
| gyrA | 9302 | c.2001C>A | synonymous_variant | 0.86 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 0.91 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 0.97 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 0.97 |
| gyrA | 9341 | c.2040C>G | synonymous_variant | 0.97 |
| gyrA | 9353 | c.2052G>C | synonymous_variant | 0.97 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>C | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>C | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9398 | c.2097T>C | synonymous_variant | 1.0 |
| gyrA | 9407 | c.2106C>G | synonymous_variant | 1.0 |
| gyrA | 9419 | c.2118T>C | synonymous_variant | 1.0 |
| gyrA | 9560 | c.2259C>G | synonymous_variant | 1.0 |
| gyrA | 9565 | p.Tyr755Phe | missense_variant | 1.0 |
| gyrA | 9572 | c.2271C>A | synonymous_variant | 1.0 |
| gyrA | 9575 | c.2274G>C | synonymous_variant | 1.0 |
| gyrA | 9583 | p.Arg761Lys | missense_variant | 1.0 |
| gyrA | 9585 | c.2284T>C | synonymous_variant | 1.0 |
| gyrA | 9593 | c.2292G>C | synonymous_variant | 1.0 |
| gyrA | 9596 | c.2295G>C | synonymous_variant | 1.0 |
| gyrA | 9597 | c.2296T>C | synonymous_variant | 1.0 |
| gyrA | 9602 | c.2301T>C | synonymous_variant | 1.0 |
| gyrA | 9626 | c.2325T>C | synonymous_variant | 1.0 |
| gyrA | 9630 | p.Val777Ile | missense_variant | 1.0 |
| gyrA | 9635 | c.2334T>C | synonymous_variant | 1.0 |
| gyrA | 9638 | c.2337C>G | synonymous_variant | 1.0 |
| gyrA | 9644 | c.2343T>C | synonymous_variant | 1.0 |
| gyrA | 9665 | c.2364A>G | synonymous_variant | 1.0 |
| gyrA | 9671 | c.2370G>A | synonymous_variant | 1.0 |
| gyrA | 9674 | c.2373T>C | synonymous_variant | 1.0 |
| gyrA | 9689 | c.2388G>C | synonymous_variant | 1.0 |
| gyrA | 9704 | c.2403T>C | synonymous_variant | 1.0 |
| gyrA | 9708 | c.2407T>C | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9725 | p.Glu808Asp | missense_variant | 1.0 |
| fgd1 | 490773 | c.-10_-9insA | upstream_gene_variant | 1.0 |
| fgd1 | 490781 | c.-2T>C | upstream_gene_variant | 1.0 |
| fgd1 | 490782 | c.-1G>C | upstream_gene_variant | 1.0 |
| fgd1 | 490792 | c.10C>T | synonymous_variant | 1.0 |
| fgd1 | 490797 | c.15G>A | synonymous_variant | 1.0 |
| fgd1 | 490800 | c.18A>T | synonymous_variant | 1.0 |
| fgd1 | 490803 | c.21T>G | synonymous_variant | 1.0 |
| fgd1 | 490815 | c.33G>C | synonymous_variant | 1.0 |
| fgd1 | 490836 | c.54C>T | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>C | synonymous_variant | 1.0 |
| fgd1 | 490866 | c.84A>G | synonymous_variant | 1.0 |
| fgd1 | 490868 | p.Ala29Asp | missense_variant | 1.0 |
| fgd1 | 490887 | c.105G>C | synonymous_variant | 1.0 |
| fgd1 | 490902 | c.120T>C | synonymous_variant | 1.0 |
| fgd1 | 490911 | c.129T>C | synonymous_variant | 1.0 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Glu | missense_variant | 1.0 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 1.0 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 1.0 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 1.0 |
| fgd1 | 490962 | c.180T>C | synonymous_variant | 1.0 |
| fgd1 | 490971 | c.189A>G | synonymous_variant | 1.0 |
| fgd1 | 490974 | c.192T>C | synonymous_variant | 1.0 |
| fgd1 | 490980 | p.Asn66Lys | missense_variant | 1.0 |
| fgd1 | 490988 | p.Leu69Gln | missense_variant | 1.0 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 1.0 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 0.96 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 0.96 |
| fgd1 | 491016 | c.234C>G | synonymous_variant | 0.96 |
| fgd1 | 491043 | c.261T>C | synonymous_variant | 0.95 |
| fgd1 | 491049 | c.267T>G | synonymous_variant | 0.95 |
| fgd1 | 491055 | c.273C>G | synonymous_variant | 0.95 |
| fgd1 | 491064 | c.282A>C | synonymous_variant | 0.94 |
| fgd1 | 491077 | p.Asn99Gly | missense_variant | 0.71 |
| fgd1 | 491082 | c.300T>C | synonymous_variant | 0.71 |
| fgd1 | 491083 | p.Val101Ile | missense_variant | 0.71 |
| fgd1 | 491091 | c.309T>G | synonymous_variant | 1.0 |
| fgd1 | 491097 | c.315G>C | synonymous_variant | 1.0 |
| fgd1 | 491106 | c.324T>C | synonymous_variant | 1.0 |
| fgd1 | 491110 | p.Ala110Ser | missense_variant | 1.0 |
| fgd1 | 491115 | c.333G>C | synonymous_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Asp | missense_variant | 1.0 |
| fgd1 | 491166 | c.384G>T | synonymous_variant | 1.0 |
| fgd1 | 491168 | p.Phe129Tyr | missense_variant | 0.97 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 0.96 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.95 |
| fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.95 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 0.94 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.94 |
| fgd1 | 491208 | c.426G>C | synonymous_variant | 0.89 |
| fgd1 | 491212 | p.Ser144Leu | missense_variant | 0.89 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 0.67 |
| fgd1 | 491235 | p.Asp151Glu | missense_variant | 0.6 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 0.75 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.89 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 0.89 |
| fgd1 | 491290 | p.Val170Ile | missense_variant | 0.89 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 0.89 |
| fgd1 | 491296 | p.Val172Ile | missense_variant | 0.89 |
| fgd1 | 491307 | c.525C>G | synonymous_variant | 1.0 |
| fgd1 | 491320 | p.Ala180Gln | missense_variant | 1.0 |
| fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491355 | c.573C>G | synonymous_variant | 1.0 |
| fgd1 | 491472 | c.690A>G | synonymous_variant | 1.0 |
| fgd1 | 491491 | p.Pro237Thr | missense_variant | 1.0 |
| fgd1 | 491499 | c.717G>C | synonymous_variant | 1.0 |
| fgd1 | 491508 | c.726A>G | synonymous_variant | 1.0 |
| fgd1 | 491509 | c.727T>C | synonymous_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Glu | missense_variant | 1.0 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 1.0 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 1.0 |
| fgd1 | 491560 | p.His260Thr | missense_variant | 1.0 |
| fgd1 | 491569 | p.Asp263His | missense_variant | 1.0 |
| fgd1 | 491578 | p.Ile266Leu | missense_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491603 | p.Ala274Glu | missense_variant | 1.0 |
| fgd1 | 491605 | c.823C>T | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| fgd1 | 491631 | c.849C>T | synonymous_variant | 1.0 |
| fgd1 | 491649 | c.867C>T | synonymous_variant | 1.0 |
| fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
| mshA | 575521 | c.174A>C | synonymous_variant | 1.0 |
| mshA | 575527 | c.180G>C | synonymous_variant | 1.0 |
| mshA | 575536 | c.189T>C | synonymous_variant | 1.0 |
| mshA | 575539 | c.192C>T | synonymous_variant | 1.0 |
| mshA | 575545 | c.198C>G | synonymous_variant | 1.0 |
| mshA | 575561 | p.Met72Val | missense_variant | 1.0 |
| mshA | 575569 | c.222A>G | synonymous_variant | 1.0 |
| mshA | 575571 | p.Ser75Thr | missense_variant | 1.0 |
| mshA | 575587 | c.240C>G | synonymous_variant | 1.0 |
| mshA | 575590 | c.243T>G | synonymous_variant | 1.0 |
| mshA | 575605 | c.258G>C | synonymous_variant | 1.0 |
| mshA | 575618 | c.271C>A | synonymous_variant | 1.0 |
| mshA | 575623 | c.276C>G | synonymous_variant | 1.0 |
| mshA | 575629 | c.282A>G | synonymous_variant | 1.0 |
| mshA | 575632 | c.285G>C | synonymous_variant | 1.0 |
| mshA | 575635 | c.288A>C | synonymous_variant | 1.0 |
| mshA | 575638 | c.291T>C | synonymous_variant | 1.0 |
| mshA | 575641 | c.294A>G | synonymous_variant | 1.0 |
| mshA | 575647 | c.300G>C | synonymous_variant | 1.0 |
| mshA | 575649 | p.Val101Ala | missense_variant | 1.0 |
| mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
| mshA | 575686 | c.339G>C | synonymous_variant | 1.0 |
| mshA | 575689 | c.342G>C | synonymous_variant | 1.0 |
| mshA | 575692 | c.345G>C | synonymous_variant | 1.0 |
| mshA | 575695 | c.348C>G | synonymous_variant | 0.93 |
| mshA | 575704 | c.357T>C | synonymous_variant | 0.91 |
| mshA | 575705 | c.358_360delTTGinsCTC | synonymous_variant | 0.91 |
| mshA | 575734 | c.387T>G | synonymous_variant | 0.95 |
| mshA | 575737 | c.390T>C | synonymous_variant | 0.95 |
| mshA | 575746 | c.399C>G | synonymous_variant | 0.94 |
| mshA | 575749 | c.402C>A | synonymous_variant | 0.94 |
| mshA | 575751 | p.Gly135Ala | missense_variant | 0.95 |
| mshA | 575771 | p.Val142Ser | missense_variant | 0.94 |
| mshA | 575779 | c.432A>G | synonymous_variant | 0.93 |
| mshA | 575785 | c.438T>C | synonymous_variant | 0.93 |
| mshA | 575788 | c.441C>T | synonymous_variant | 0.93 |
| mshA | 575806 | c.459G>C | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 0.95 |
| mshA | 575824 | c.477T>G | synonymous_variant | 1.0 |
| mshA | 575833 | c.486C>G | synonymous_variant | 1.0 |
| mshA | 575842 | c.495G>C | synonymous_variant | 1.0 |
| mshA | 575851 | c.504C>G | synonymous_variant | 1.0 |
| mshA | 575864 | c.517T>C | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>G | synonymous_variant | 1.0 |
| mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
| mshA | 575896 | c.549G>C | synonymous_variant | 1.0 |
| mshA | 575905 | c.558G>C | synonymous_variant | 1.0 |
| mshA | 575908 | c.561A>G | synonymous_variant | 1.0 |
| mshA | 575920 | c.573C>G | synonymous_variant | 1.0 |
| mshA | 575924 | p.Gly193Thr | missense_variant | 1.0 |
| mshA | 575929 | c.582C>G | synonymous_variant | 0.94 |
| mshA | 575944 | c.597T>C | synonymous_variant | 0.94 |
| mshA | 575965 | c.618C>G | synonymous_variant | 0.94 |
| mshA | 575977 | c.630G>C | synonymous_variant | 0.88 |
| mshA | 575980 | c.633T>C | synonymous_variant | 0.88 |
| mshA | 576362 | c.1015T>C | synonymous_variant | 1.0 |
| mshA | 576367 | c.1020T>C | synonymous_variant | 1.0 |
| mshA | 576370 | c.1023G>C | synonymous_variant | 1.0 |
| mshA | 576373 | c.1026G>C | synonymous_variant | 1.0 |
| mshA | 576376 | c.1029G>C | synonymous_variant | 1.0 |
| mshA | 576385 | c.1038T>C | synonymous_variant | 1.0 |
| mshA | 576388 | c.1041G>C | synonymous_variant | 1.0 |
| mshA | 576394 | c.1047G>C | synonymous_variant | 1.0 |
| mshA | 576421 | c.1074T>C | synonymous_variant | 1.0 |
| mshA | 576424 | c.1077T>G | synonymous_variant | 1.0 |
| mshA | 576425 | p.Val360Leu | missense_variant | 1.0 |
| mshA | 576433 | c.1086C>G | synonymous_variant | 1.0 |
| mshA | 576436 | c.1089A>G | synonymous_variant | 1.0 |
| mshA | 576448 | c.1101A>G | synonymous_variant | 1.0 |
| mshA | 576463 | c.1116G>C | synonymous_variant | 1.0 |
| mshA | 576469 | c.1122G>C | synonymous_variant | 1.0 |
| mshA | 576472 | c.1125C>G | synonymous_variant | 1.0 |
| mshA | 576476 | c.1129C>T | synonymous_variant | 1.0 |
| mshA | 576484 | c.1137C>G | synonymous_variant | 1.0 |
| mshA | 576487 | c.1140G>C | synonymous_variant | 1.0 |
| mshA | 576628 | c.1281G>C | synonymous_variant | 1.0 |
| mshA | 576634 | c.1287G>C | synonymous_variant | 1.0 |
| mshA | 576640 | p.Glu431Asp | missense_variant | 1.0 |
| mshA | 576641 | p.Asn432His | missense_variant | 1.0 |
| mshA | 576663 | p.Ala439Gly | missense_variant | 1.0 |
| mshA | 576667 | c.1320T>C | synonymous_variant | 1.0 |
| mshA | 576673 | c.1326G>A | synonymous_variant | 1.0 |
| mshA | 576676 | c.1329T>C | synonymous_variant | 1.0 |
| mshA | 576679 | c.1332G>C | synonymous_variant | 1.0 |
| mshA | 576683 | p.Gly446Arg | missense_variant | 1.0 |
| mshA | 576688 | p.Glu447Asp | missense_variant | 1.0 |
| mshA | 576693 | p.Asn449Thr | missense_variant | 1.0 |
| ccsA | 619693 | c.-198G>C | upstream_gene_variant | 0.6 |
| ccsA | 619696 | c.-195C>G | upstream_gene_variant | 0.6 |
| ccsA | 619697 | c.-194_-192delAGGinsCGC | upstream_gene_variant | 0.6 |
| ccsA | 619889 | c.-2_1delGATinsAAA | initiator_codon_variant | 1.0 |
| ccsA | 619899 | c.9G>C | synonymous_variant | 1.0 |
| ccsA | 619900 | p.Leu4Val | missense_variant | 1.0 |
| ccsA | 619912 | p.Val8Ile | missense_variant | 1.0 |
| ccsA | 619932 | c.42C>G | synonymous_variant | 0.94 |
| ccsA | 619962 | c.72G>C | synonymous_variant | 0.92 |
| ccsA | 619969 | p.Val27Ile | missense_variant | 0.9 |
| ccsA | 619989 | c.99G>C | synonymous_variant | 0.67 |
| ccsA | 619990 | p.Phe34Val | missense_variant | 0.67 |
| ccsA | 619996 | p.Phe36Leu | missense_variant | 0.67 |
| ccsA | 620145 | c.255T>C | synonymous_variant | 0.5 |
| ccsA | 620157 | c.267G>C | synonymous_variant | 0.86 |
| ccsA | 620160 | c.270A>G | synonymous_variant | 0.86 |
| ccsA | 620163 | c.273G>A | synonymous_variant | 0.86 |
| ccsA | 620169 | c.279G>C | synonymous_variant | 0.91 |
| ccsA | 620173 | p.Val95Ile | missense_variant | 0.92 |
| ccsA | 620198 | p.Gln103Leu | missense_variant | 0.95 |
| ccsA | 620208 | c.318G>C | synonymous_variant | 0.97 |
| ccsA | 620245 | p.Leu119Met | missense_variant | 0.97 |
| ccsA | 620249 | p.Ser120Cys | missense_variant | 0.94 |
| ccsA | 620253 | c.363G>C | synonymous_variant | 0.97 |
| ccsA | 620256 | c.366C>G | synonymous_variant | 0.97 |
| ccsA | 620257 | p.Ile123Leu | missense_variant | 0.97 |
| ccsA | 620265 | c.375C>G | synonymous_variant | 0.97 |
| ccsA | 620267 | p.Ala126Val | missense_variant | 0.97 |
| ccsA | 620283 | c.393T>C | synonymous_variant | 1.0 |
| ccsA | 620284 | p.Ala132Pro | missense_variant | 1.0 |
| ccsA | 620288 | p.Arg133Gln | missense_variant | 1.0 |
| ccsA | 620295 | c.405G>C | synonymous_variant | 1.0 |
| ccsA | 620307 | c.417C>G | synonymous_variant | 1.0 |
| ccsA | 620319 | c.429C>G | synonymous_variant | 1.0 |
| ccsA | 620340 | c.450C>G | synonymous_variant | 1.0 |
| ccsA | 620349 | c.459A>C | synonymous_variant | 1.0 |
| ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
| ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620412 | c.522T>C | synonymous_variant | 0.98 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 0.98 |
| ccsA | 620427 | c.537C>G | synonymous_variant | 0.98 |
| ccsA | 620433 | c.543C>G | synonymous_variant | 0.98 |
| ccsA | 620439 | c.549T>C | synonymous_variant | 0.98 |
| ccsA | 620445 | c.555A>G | synonymous_variant | 0.97 |
| ccsA | 620460 | c.570T>C | synonymous_variant | 0.97 |
| ccsA | 620461 | p.Val191Ile | missense_variant | 0.96 |
| ccsA | 620481 | c.591T>G | synonymous_variant | 0.86 |
| ccsA | 620482 | p.Val198Leu | missense_variant | 0.8 |
| ccsA | 620490 | c.600A>C | synonymous_variant | 0.67 |
| ccsA | 620493 | c.603G>A | synonymous_variant | 0.67 |
| ccsA | 620496 | c.606G>C | synonymous_variant | 0.67 |
| ccsA | 620502 | c.612T>G | synonymous_variant | 1.0 |
| ccsA | 620583 | c.693G>C | synonymous_variant | 0.67 |
| ccsA | 620597 | p.Ala236Gly | missense_variant | 0.93 |
| ccsA | 620604 | c.714C>G | synonymous_variant | 0.94 |
| ccsA | 620607 | c.717T>A | synonymous_variant | 0.95 |
| ccsA | 620625 | c.735A>C | synonymous_variant | 0.96 |
| ccsA | 620631 | c.741T>C | synonymous_variant | 1.0 |
| ccsA | 620646 | c.756G>A | synonymous_variant | 1.0 |
| ccsA | 620647 | p.Glu253Gln | missense_variant | 1.0 |
| ccsA | 620652 | c.762C>G | synonymous_variant | 1.0 |
| ccsA | 620661 | c.771C>G | synonymous_variant | 1.0 |
| ccsA | 620685 | c.795G>A | synonymous_variant | 1.0 |
| ccsA | 620694 | c.804C>G | synonymous_variant | 1.0 |
| ccsA | 620703 | c.813G>A | synonymous_variant | 1.0 |
| ccsA | 620709 | c.819G>C | synonymous_variant | 1.0 |
| ccsA | 620712 | c.822G>C | synonymous_variant | 1.0 |
| ccsA | 620718 | c.828G>C | synonymous_variant | 1.0 |
| ccsA | 620721 | c.831G>C | synonymous_variant | 1.0 |
| ccsA | 620733 | c.843G>C | synonymous_variant | 1.0 |
| ccsA | 620734 | c.844C>A | synonymous_variant | 1.0 |
| ccsA | 620739 | c.849A>G | synonymous_variant | 1.0 |
| ccsA | 620745 | c.855G>C | synonymous_variant | 1.0 |
| ccsA | 620748 | c.858T>A | synonymous_variant | 1.0 |
| ccsA | 620757 | c.867C>T | synonymous_variant | 1.0 |
| ccsA | 620766 | c.876C>G | synonymous_variant | 1.0 |
| ccsA | 620769 | c.879C>G | synonymous_variant | 1.0 |
| ccsA | 620778 | c.888T>C | synonymous_variant | 1.0 |
| ccsA | 620783 | p.Ala298Val | missense_variant | 1.0 |
| ccsA | 620787 | c.897C>T | synonymous_variant | 1.0 |
| ccsA | 620809 | c.919C>T | synonymous_variant | 1.0 |
| ccsA | 620823 | c.933C>T | synonymous_variant | 1.0 |
| ccsA | 620829 | c.939G>C | synonymous_variant | 1.0 |
| ccsA | 620844 | c.954C>T | synonymous_variant | 1.0 |
| rpoB | 759609 | c.-198C>A | upstream_gene_variant | 0.29 |
| rpoB | 759629 | c.-178T>A | upstream_gene_variant | 1.0 |
| rpoB | 759636 | c.-171C>T | upstream_gene_variant | 1.0 |
| rpoB | 759641 | c.-166T>A | upstream_gene_variant | 1.0 |
| rpoB | 759644 | c.-163T>A | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 760046 | c.240G>C | synonymous_variant | 0.67 |
| rpoB | 760061 | c.255C>T | synonymous_variant | 0.67 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 0.5 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 0.5 |
| rpoB | 760073 | c.267G>C | synonymous_variant | 0.75 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 0.88 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 0.91 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 0.96 |
| rpoB | 760118 | c.312T>C | synonymous_variant | 0.96 |
| rpoB | 760121 | c.315T>C | synonymous_variant | 0.97 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 0.97 |
| rpoB | 760139 | c.333A>G | synonymous_variant | 0.97 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 0.97 |
| rpoB | 760148 | p.Asp114Glu | missense_variant | 0.97 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760271 | c.465C>G | synonymous_variant | 0.95 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 0.96 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 0.96 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 0.96 |
| rpoB | 760313 | c.507G>C | synonymous_variant | 0.96 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>C | synonymous_variant | 1.0 |
| rpoB | 760343 | c.537G>C | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760370 | c.564C>G | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760380 | p.Thr192Leu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760520 | c.714C>G | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243His | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760566 | p.Ser254Ala | missense_variant | 1.0 |
| rpoB | 760567 | c.762delG | frameshift_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 0.97 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 0.98 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 0.96 |
| rpoB | 760661 | c.855A>G | synonymous_variant | 0.96 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 0.95 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 0.95 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 0.95 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 0.94 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 0.97 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 0.95 |
| rpoB | 760754 | c.948G>C | synonymous_variant | 1.0 |
| rpoB | 760755 | p.His317Asn | missense_variant | 1.0 |
| rpoB | 760763 | c.957C>G | synonymous_variant | 1.0 |
| rpoB | 760764 | p.Glu320Gln | missense_variant | 1.0 |
| rpoB | 760769 | c.963C>G | synonymous_variant | 1.0 |
| rpoB | 760781 | c.975G>C | synonymous_variant | 1.0 |
| rpoB | 760787 | c.981G>C | synonymous_variant | 1.0 |
| rpoB | 760793 | c.987A>G | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760859 | c.1053T>G | synonymous_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760869 | p.Val355Thr | missense_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760920 | c.1114C>T | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760931 | c.1125C>G | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>G | synonymous_variant | 0.98 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 0.98 |
| rpoB | 761021 | c.1215G>C | synonymous_variant | 0.98 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 0.98 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 0.98 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 0.98 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 0.98 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 0.98 |
| rpoB | 761124 | c.1318C>T | synonymous_variant | 0.98 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 0.98 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 0.98 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 0.98 |
| rpoB | 761165 | c.1359G>T | synonymous_variant | 0.98 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 0.98 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 0.98 |
| rpoB | 761183 | c.1377T>G | synonymous_variant | 0.98 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 0.97 |
| rpoB | 761192 | c.1386C>G | synonymous_variant | 0.95 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 0.98 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 0.96 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 0.96 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 0.97 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 0.96 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761361 | c.1555_1556delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761435 | c.1629T>C | synonymous_variant | 1.0 |
| rpoB | 761437 | p.Ala544Gly | missense_variant | 1.0 |
| rpoB | 761444 | c.1638T>C | synonymous_variant | 1.0 |
| rpoB | 761447 | c.1641C>G | synonymous_variant | 1.0 |
| rpoB | 761452 | p.Val549Ala | missense_variant | 1.0 |
| rpoB | 761457 | p.Pro551Ala | missense_variant | 1.0 |
| rpoB | 761465 | c.1659G>C | synonymous_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761504 | c.1698C>G | synonymous_variant | 1.0 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761600 | c.1794T>G | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 0.98 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761693 | c.1887G>C | synonymous_variant | 1.0 |
| rpoB | 761711 | c.1905C>T | synonymous_variant | 1.0 |
| rpoB | 761732 | c.1926C>G | synonymous_variant | 1.0 |
| rpoB | 761735 | c.1929C>G | synonymous_variant | 1.0 |
| rpoB | 761747 | c.1941G>C | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761785 | p.Thr660Ser | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761815 | p.Ala670Glu | missense_variant | 1.0 |
| rpoB | 761834 | c.2028T>G | synonymous_variant | 1.0 |
| rpoB | 761848 | p.Cys681Ser | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>A | synonymous_variant | 1.0 |
| rpoB | 761867 | c.2061C>T | synonymous_variant | 1.0 |
| rpoB | 761870 | p.Asp688Glu | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761891 | c.2085G>C | synonymous_variant | 1.0 |
| rpoB | 761903 | c.2097T>G | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761930 | c.2124G>C | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761972 | c.2166C>G | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762128 | c.2322G>A | synonymous_variant | 1.0 |
| rpoB | 762138 | c.2332C>T | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762197 | c.2391C>G | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762350 | c.2544C>G | synonymous_variant | 1.0 |
| rpoB | 762353 | c.2547C>T | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| rpoC | 762395 | c.-975G>C | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762407 | c.-963G>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762486 | p.Pro894Ala | missense_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.96 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 0.96 |
| rpoC | 762521 | c.-849C>G | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762575 | c.-795C>T | upstream_gene_variant | 1.0 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 1.0 |
| rpoC | 762582 | c.-788_-786delTTGinsCTC | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762785 | p.Asp993Glu | missense_variant | 1.0 |
| rpoB | 762795 | p.Asp997Asn | missense_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762813 | p.Met1003Val | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>G | upstream_gene_variant | 1.0 |
| rpoC | 762839 | c.-531G>A | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 1.0 |
| rpoC | 762947 | c.-423C>G | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762977 | c.-393C>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763013 | c.-357C>T | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>C | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoC | 763208 | c.-162T>C | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763217 | c.-153G>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763229 | c.-141G>C | upstream_gene_variant | 1.0 |
| rpoC | 763235 | c.-135A>G | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763247 | c.-123G>A | upstream_gene_variant | 1.0 |
| rpoC | 763256 | c.-114G>A | upstream_gene_variant | 1.0 |
| rpoC | 763262 | c.-108C>T | upstream_gene_variant | 1.0 |
| rpoC | 763274 | c.-96G>C | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>A | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>G | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>A | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
| rpoC | 763792 | p.Glu141Asp | missense_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
| rpoC | 763831 | c.462A>G | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | missense_variant | 1.0 |
| rpoC | 763853 | p.Val162Ile | missense_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 0.97 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>T | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
| rpoC | 763978 | c.609C>G | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 0.95 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764071 | c.702G>C | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764095 | c.726C>G | synonymous_variant | 1.0 |
| rpoC | 764104 | c.735C>G | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 1.0 |
| rpoC | 764182 | p.Asp271Glu | missense_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ile | missense_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764209 | c.840C>G | synonymous_variant | 1.0 |
| rpoC | 764215 | c.846A>T | synonymous_variant | 1.0 |
| rpoC | 764218 | c.849C>T | synonymous_variant | 1.0 |
| rpoC | 764254 | c.885G>C | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 0.98 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 0.99 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 0.99 |
| rpoC | 764338 | c.969G>A | synonymous_variant | 0.98 |
| rpoC | 764344 | c.975C>G | synonymous_variant | 0.97 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 0.97 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 0.97 |
| rpoC | 764377 | c.1008C>G | synonymous_variant | 0.97 |
| rpoC | 764383 | c.1014C>G | synonymous_variant | 0.97 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.97 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.96 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 0.98 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 0.98 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 0.98 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 0.98 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 0.96 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 0.98 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 0.98 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 0.96 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 0.94 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 0.97 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 0.97 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 0.97 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 0.97 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 0.99 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.99 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 0.99 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764695 | c.1326T>C | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>C | synonymous_variant | 1.0 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 0.99 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 0.99 |
| rpoC | 764803 | c.1434C>G | synonymous_variant | 0.99 |
| rpoC | 764809 | c.1440C>A | synonymous_variant | 0.99 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 0.99 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 0.99 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 0.99 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>A | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765052 | c.1683C>G | synonymous_variant | 1.0 |
| rpoC | 765073 | c.1704G>C | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>A | synonymous_variant | 1.0 |
| rpoC | 765085 | c.1716T>C | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>T | synonymous_variant | 1.0 |
| rpoC | 765115 | c.1746G>C | synonymous_variant | 1.0 |
| rpoC | 765121 | c.1752G>C | synonymous_variant | 1.0 |
| rpoC | 765129 | p.Tyr587Phe | missense_variant | 1.0 |
| rpoC | 765133 | c.1764G>C | synonymous_variant | 1.0 |
| rpoC | 765283 | c.1914C>G | synonymous_variant | 1.0 |
| rpoC | 765292 | c.1923G>T | synonymous_variant | 1.0 |
| rpoC | 765298 | c.1929G>C | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
| rpoC | 765304 | p.Glu645Asp | missense_variant | 1.0 |
| rpoC | 765313 | c.1944C>G | synonymous_variant | 1.0 |
| rpoC | 765317 | c.1948_1950delCTAinsTTG | synonymous_variant | 1.0 |
| rpoC | 765326 | p.His653Ala | missense_variant | 1.0 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
| rpoC | 765334 | c.1965C>T | synonymous_variant | 1.0 |
| rpoC | 765346 | c.1977C>T | synonymous_variant | 1.0 |
| rpoC | 765349 | c.1980T>C | synonymous_variant | 1.0 |
| rpoC | 765367 | c.1998C>G | synonymous_variant | 1.0 |
| rpoC | 765371 | c.2002C>T | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 1.0 |
| rpoC | 765397 | c.2028G>A | synonymous_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Ser | missense_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765493 | c.2124G>C | synonymous_variant | 0.98 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 0.98 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 0.98 |
| rpoC | 765544 | c.2175C>T | synonymous_variant | 0.98 |
| rpoC | 765550 | c.2181C>T | synonymous_variant | 0.98 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 0.98 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 0.98 |
| rpoC | 765559 | c.2190G>C | synonymous_variant | 0.98 |
| rpoC | 765592 | c.2223C>T | synonymous_variant | 1.0 |
| rpoC | 765611 | p.His748Ala | missense_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765689 | c.2320C>T | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765727 | c.2358T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 0.99 |
| rpoC | 765739 | c.2370G>C | synonymous_variant | 0.99 |
| rpoC | 765752 | p.Asp795Ser | missense_variant | 0.98 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 0.99 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 0.98 |
| rpoC | 765787 | c.2418C>T | synonymous_variant | 0.98 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 0.98 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 0.98 |
| rpoC | 765805 | c.2436C>G | synonymous_variant | 0.98 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 0.98 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 0.99 |
| rpoC | 765871 | c.2502T>C | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765908 | c.2539C>T | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 0.98 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.98 |
| rpoC | 766043 | p.Gln892Glu | missense_variant | 0.93 |
| rpoC | 766054 | c.2685C>G | synonymous_variant | 0.94 |
| rpoC | 766061 | p.Val898Thr | missense_variant | 0.92 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 0.9 |
| rpoC | 766087 | c.2718C>G | synonymous_variant | 0.9 |
| rpoC | 766093 | c.2724C>G | synonymous_variant | 0.93 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 0.93 |
| rpoC | 766105 | c.2736C>T | synonymous_variant | 0.93 |
| rpoC | 766129 | c.2760C>G | synonymous_variant | 1.0 |
| rpoC | 766135 | c.2766G>A | synonymous_variant | 1.0 |
| rpoC | 766141 | c.2772C>T | synonymous_variant | 1.0 |
| rpoC | 766147 | c.2778C>T | synonymous_variant | 1.0 |
| rpoC | 766148 | p.Thr927Ser | missense_variant | 1.0 |
| rpoC | 766159 | c.2790C>G | synonymous_variant | 1.0 |
| rpoC | 766168 | c.2799C>G | synonymous_variant | 1.0 |
| rpoC | 766178 | p.Ile937Val | missense_variant | 1.0 |
| rpoC | 766185 | p.Glu939Ala | missense_variant | 1.0 |
| rpoC | 766189 | c.2820T>C | synonymous_variant | 1.0 |
| rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
| rpoC | 766274 | p.Ala969Thr | missense_variant | 1.0 |
| rpoC | 766279 | c.2910C>G | synonymous_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766288 | c.2919C>A | synonymous_variant | 1.0 |
| rpoC | 766291 | c.2922G>C | synonymous_variant | 1.0 |
| rpoC | 766303 | c.2934C>T | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>G | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766327 | c.2958C>A | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766366 | c.2997C>G | synonymous_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766447 | c.3078T>C | synonymous_variant | 0.97 |
| rpoC | 766462 | c.3093G>T | synonymous_variant | 0.98 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 0.97 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 0.97 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 0.97 |
| rpoC | 766522 | c.3153C>G | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766530 | p.Arg1054Gln | missense_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766543 | c.3174C>T | synonymous_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>G | synonymous_variant | 1.0 |
| rpoC | 766583 | p.Gly1072Ser | missense_variant | 1.0 |
| rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>C | synonymous_variant | 1.0 |
| rpoC | 766597 | c.3228C>G | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766618 | c.3249G>T | synonymous_variant | 1.0 |
| rpoC | 766630 | c.3261G>C | synonymous_variant | 1.0 |
| rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766666 | c.3297C>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766702 | c.3333G>C | synonymous_variant | 0.99 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766733 | c.3364_3366delCTGinsTTA | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766750 | c.3381C>G | synonymous_variant | 0.99 |
| rpoC | 766753 | c.3384C>T | synonymous_variant | 0.95 |
| rpoC | 766754 | p.Glu1129Gln | missense_variant | 0.98 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766777 | c.3408C>G | synonymous_variant | 0.98 |
| rpoC | 766781 | p.Val1138Thr | missense_variant | 0.98 |
| rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766882 | c.3513C>T | synonymous_variant | 1.0 |
| rpoC | 766883 | p.Ser1172Ala | missense_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766918 | c.3549C>T | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>C | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766978 | c.3609C>T | synonymous_variant | 1.0 |
| rpoC | 766981 | c.3612T>C | synonymous_variant | 1.0 |
| rpoC | 767020 | c.3651C>G | synonymous_variant | 1.0 |
| rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767105 | p.Asn1246Gln | missense_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>A | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 0.97 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 0.97 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Gln | missense_variant | 1.0 |
| rpoC | 767275 | c.3906T>C | synonymous_variant | 1.0 |
| rpoC | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>G | synonymous_variant | 1.0 |
| rpoC | 767296 | c.3927C>T | synonymous_variant | 1.0 |
| rpoC | 767302 | c.3933C>G | synonymous_variant | 1.0 |
| mmpL5 | 775909 | p.Leu858Phe | missense_variant | 1.0 |
| mmpL5 | 775913 | p.Ala856Ser | missense_variant | 1.0 |
| mmpL5 | 775916 | c.2565T>G | synonymous_variant | 1.0 |
| mmpL5 | 775937 | p.Ala848Ser | missense_variant | 1.0 |
| mmpL5 | 775951 | c.2530C>T | synonymous_variant | 1.0 |
| mmpL5 | 776060 | c.2421C>G | synonymous_variant | 1.0 |
| mmpL5 | 776072 | c.2409C>G | synonymous_variant | 1.0 |
| mmpL5 | 776076 | p.Ala802Phe | missense_variant | 1.0 |
| mmpL5 | 776084 | c.2397C>G | synonymous_variant | 1.0 |
| mmpL5 | 776093 | c.2388C>A | synonymous_variant | 1.0 |
| mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
| mmpL5 | 776102 | p.Ile793Val | missense_variant | 1.0 |
| mmpL5 | 776107 | c.2374C>T | synonymous_variant | 1.0 |
| mmpL5 | 776127 | p.Cys785Thr | missense_variant | 1.0 |
| mmpL5 | 776130 | p.Leu784Ala | missense_variant | 1.0 |
| mmpL5 | 776141 | c.2340A>C | synonymous_variant | 1.0 |
| mmpL5 | 776150 | p.Met777Ile | missense_variant | 1.0 |
| mmpL5 | 776155 | c.2326T>C | synonymous_variant | 1.0 |
| mmpL5 | 776312 | c.2169A>G | synonymous_variant | 1.0 |
| mmpL5 | 776319 | c.2161_2162delAGinsTC | synonymous_variant | 1.0 |
| mmpL5 | 776327 | p.Phe718Leu | missense_variant | 1.0 |
| mmpL5 | 776333 | c.2148G>C | synonymous_variant | 1.0 |
| mmpL5 | 776356 | p.Leu709Ile | missense_variant | 1.0 |
| mmpL5 | 776647 | p.Val612Ile | missense_variant | 0.5 |
| mmpL5 | 776653 | p.Ile610Phe | missense_variant | 0.5 |
| mmpL5 | 776654 | c.1827A>T | synonymous_variant | 1.0 |
| mmpL5 | 776665 | p.Thr606Ser | missense_variant | 0.29 |
| mmpL5 | 776674 | p.Val603Leu | missense_variant | 0.36 |
| mmpL5 | 776678 | c.1803G>C | synonymous_variant | 0.5 |
| mmpL5 | 776687 | p.Trp598Phe | missense_variant | 0.71 |
| mmpL5 | 776693 | p.Val596Met | missense_variant | 0.5 |
| mmpL5 | 776706 | p.Tyr592Phe | missense_variant | 0.29 |
| mmpL5 | 776717 | c.1764A>G | synonymous_variant | 1.0 |
| mmpL5 | 776740 | p.Ile581Val | missense_variant | 0.5 |
| mmpL5 | 776741 | c.1740C>G | synonymous_variant | 1.0 |
| mmpL5 | 776744 | c.1737C>G | synonymous_variant | 0.5 |
| mmpL5 | 776753 | c.1728T>C | synonymous_variant | 0.75 |
| mmpL5 | 776756 | p.Asp575Glu | missense_variant | 0.5 |
| mmpL5 | 776762 | c.1719T>C | synonymous_variant | 0.5 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
| rpsL | 781605 | p.Ile16Val | missense_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 0.98 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 0.98 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 0.94 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 0.94 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 0.96 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 0.96 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781880 | c.321C>G | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.87 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.86 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.89 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.86 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.88 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800815 | c.7C>A | synonymous_variant | 1.0 |
| rplC | 800820 | c.12G>A | synonymous_variant | 1.0 |
| rplC | 800829 | c.21C>G | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800874 | c.66A>G | synonymous_variant | 1.0 |
| rplC | 800877 | c.69A>C | synonymous_variant | 1.0 |
| rplC | 800880 | c.72A>C | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800904 | c.96G>A | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| rplC | 800922 | c.114C>G | synonymous_variant | 1.0 |
| rplC | 800931 | c.123G>C | synonymous_variant | 1.0 |
| rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
| rplC | 800946 | c.138T>C | synonymous_variant | 1.0 |
| rplC | 800949 | c.141T>C | synonymous_variant | 1.0 |
| rplC | 800964 | c.156G>C | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 801109 | c.301T>C | synonymous_variant | 1.0 |
| rplC | 801114 | c.306C>G | synonymous_variant | 1.0 |
| rplC | 801132 | c.324T>C | synonymous_variant | 1.0 |
| rplC | 801136 | p.Ser110Ala | missense_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801150 | c.342G>C | synonymous_variant | 1.0 |
| rplC | 801153 | c.345G>C | synonymous_variant | 1.0 |
| rplC | 801156 | c.348T>C | synonymous_variant | 1.0 |
| rplC | 801159 | c.351C>G | synonymous_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 0.97 |
| rplC | 801174 | c.366T>C | synonymous_variant | 0.97 |
| rplC | 801222 | c.414T>C | synonymous_variant | 0.98 |
| rplC | 801228 | c.420T>C | synonymous_variant | 0.98 |
| rplC | 801246 | c.438C>T | synonymous_variant | 0.98 |
| rplC | 801252 | c.444G>C | synonymous_variant | 0.98 |
| rplC | 801264 | c.456C>T | synonymous_variant | 0.97 |
| rplC | 801267 | c.459A>C | synonymous_variant | 1.0 |
| rplC | 801276 | c.468G>C | synonymous_variant | 1.0 |
| rplC | 801282 | c.474G>C | synonymous_variant | 1.0 |
| rplC | 801285 | c.477G>C | synonymous_variant | 1.0 |
| rplC | 801300 | c.492C>G | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 0.97 |
| rplC | 801324 | c.516T>C | synonymous_variant | 0.97 |
| rplC | 801336 | c.528C>G | synonymous_variant | 0.97 |
| rplC | 801341 | p.Leu178Gln | missense_variant | 0.97 |
| rplC | 801348 | c.540T>G | synonymous_variant | 0.97 |
| rplC | 801349 | p.Leu181Val | missense_variant | 0.97 |
| rplC | 801357 | c.549T>C | synonymous_variant | 0.97 |
| rplC | 801363 | c.555C>T | synonymous_variant | 0.98 |
| rplC | 801367 | p.Ala187Pro | missense_variant | 0.98 |
| rplC | 801387 | c.579G>C | synonymous_variant | 0.95 |
| rplC | 801396 | c.588T>C | synonymous_variant | 0.93 |
| rplC | 801402 | c.594T>C | synonymous_variant | 0.92 |
| rplC | 801405 | c.597T>C | synonymous_variant | 0.92 |
| rplC | 801423 | c.615G>C | synonymous_variant | 0.92 |
| rplC | 801426 | c.618C>G | synonymous_variant | 0.91 |
| rplC | 801427 | p.Met207Val | missense_variant | 0.91 |
| rplC | 801438 | c.630T>C | synonymous_variant | 0.91 |
| rplC | 801442 | p.Ile212Val | missense_variant | 0.91 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 0.75 |
| fbiC | 1303184 | p.Ser85Thr | missense_variant | 1.0 |
| fbiC | 1303188 | c.258T>C | synonymous_variant | 1.0 |
| fbiC | 1303209 | c.279G>C | synonymous_variant | 1.0 |
| fbiC | 1303210 | p.Val94Ile | missense_variant | 1.0 |
| fbiC | 1303217 | p.Arg96His | missense_variant | 1.0 |
| fbiC | 1303219 | c.289_291delTTAinsCTG | synonymous_variant | 1.0 |
| fbiC | 1303227 | c.297G>C | synonymous_variant | 1.0 |
| fbiC | 1303233 | c.303T>C | synonymous_variant | 1.0 |
| fbiC | 1303242 | c.312T>C | synonymous_variant | 1.0 |
| fbiC | 1303254 | c.324C>G | synonymous_variant | 1.0 |
| fbiC | 1303257 | c.327C>G | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303476 | c.546G>C | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303492 | c.562T>C | synonymous_variant | 1.0 |
| fbiC | 1303506 | c.576C>T | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303515 | c.585G>C | synonymous_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303575 | c.645G>C | synonymous_variant | 1.0 |
| fbiC | 1303581 | c.651G>C | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>G | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303593 | c.663G>C | synonymous_variant | 1.0 |
| fbiC | 1303594 | c.664C>T | synonymous_variant | 1.0 |
| fbiC | 1303602 | c.672A>G | synonymous_variant | 1.0 |
| fbiC | 1303608 | c.678G>A | synonymous_variant | 1.0 |
| fbiC | 1303611 | c.681G>C | synonymous_variant | 1.0 |
| fbiC | 1303614 | c.684C>T | synonymous_variant | 1.0 |
| fbiC | 1303617 | c.687C>G | synonymous_variant | 1.0 |
| fbiC | 1303623 | c.693C>T | synonymous_variant | 1.0 |
| fbiC | 1303632 | c.702T>G | synonymous_variant | 1.0 |
| fbiC | 1303638 | c.708A>G | synonymous_variant | 1.0 |
| fbiC | 1303647 | c.717G>C | synonymous_variant | 1.0 |
| fbiC | 1303650 | c.720G>C | synonymous_variant | 1.0 |
| fbiC | 1303659 | c.729T>C | synonymous_variant | 1.0 |
| fbiC | 1303661 | p.Val244Ala | missense_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303681 | c.751_753delTTGinsCTC | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303689 | c.759T>C | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303728 | c.798G>C | synonymous_variant | 1.0 |
| fbiC | 1303731 | c.801A>G | synonymous_variant | 1.0 |
| fbiC | 1303732 | p.Ser268Ala | missense_variant | 1.0 |
| fbiC | 1303737 | c.807G>A | synonymous_variant | 1.0 |
| fbiC | 1303746 | c.816T>C | synonymous_variant | 1.0 |
| fbiC | 1303750 | c.820_822delTTAinsCTG | synonymous_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303788 | c.858T>C | synonymous_variant | 1.0 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 0.97 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 0.97 |
| fbiC | 1303827 | c.897A>G | synonymous_variant | 0.97 |
| fbiC | 1303845 | c.915C>G | synonymous_variant | 0.97 |
| fbiC | 1303846 | p.Phe306Val | missense_variant | 0.97 |
| fbiC | 1303854 | c.924T>C | synonymous_variant | 0.97 |
| fbiC | 1303857 | c.927C>G | synonymous_variant | 0.97 |
| fbiC | 1303860 | c.930A>G | synonymous_variant | 0.97 |
| fbiC | 1303869 | c.939T>C | synonymous_variant | 0.97 |
| fbiC | 1303884 | c.954T>C | synonymous_variant | 0.96 |
| fbiC | 1303893 | c.963G>C | synonymous_variant | 1.0 |
| fbiC | 1303896 | c.966G>C | synonymous_variant | 1.0 |
| fbiC | 1303902 | c.972G>C | synonymous_variant | 1.0 |
| fbiC | 1303908 | c.978C>T | synonymous_variant | 0.98 |
| fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.97 |
| fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.97 |
| fbiC | 1303952 | p.Asp341Ala | missense_variant | 0.97 |
| fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.97 |
| fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.97 |
| fbiC | 1303969 | p.Val347Ile | missense_variant | 0.97 |
| fbiC | 1303977 | c.1047C>G | synonymous_variant | 0.97 |
| fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.97 |
| fbiC | 1303986 | c.1056C>T | synonymous_variant | 0.97 |
| fbiC | 1304001 | c.1071C>T | synonymous_variant | 0.94 |
| fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.93 |
| fbiC | 1304007 | c.1077G>C | synonymous_variant | 0.89 |
| fbiC | 1304008 | c.1078T>C | synonymous_variant | 1.0 |
| fbiC | 1304019 | c.1089C>T | synonymous_variant | 1.0 |
| fbiC | 1304022 | c.1092T>C | synonymous_variant | 1.0 |
| fbiC | 1304034 | c.1104A>G | synonymous_variant | 1.0 |
| fbiC | 1304040 | c.1110C>G | synonymous_variant | 1.0 |
| fbiC | 1304049 | c.1119T>G | synonymous_variant | 1.0 |
| fbiC | 1304050 | c.1120T>C | synonymous_variant | 1.0 |
| fbiC | 1304055 | p.Asp375Glu | missense_variant | 1.0 |
| fbiC | 1304059 | c.1129C>T | synonymous_variant | 1.0 |
| fbiC | 1304064 | c.1134G>C | synonymous_variant | 1.0 |
| fbiC | 1304079 | c.1149A>G | synonymous_variant | 1.0 |
| fbiC | 1304085 | c.1155C>T | synonymous_variant | 1.0 |
| fbiC | 1304091 | p.Asp387Glu | missense_variant | 1.0 |
| fbiC | 1304092 | p.Met388Leu | missense_variant | 1.0 |
| fbiC | 1304115 | c.1185A>G | synonymous_variant | 1.0 |
| fbiC | 1304121 | c.1191A>G | synonymous_variant | 1.0 |
| fbiC | 1304127 | c.1197A>G | synonymous_variant | 1.0 |
| fbiC | 1304139 | c.1209G>C | synonymous_variant | 1.0 |
| fbiC | 1304142 | c.1212G>C | synonymous_variant | 1.0 |
| fbiC | 1304151 | c.1221C>T | synonymous_variant | 1.0 |
| fbiC | 1304166 | c.1236A>G | synonymous_variant | 1.0 |
| fbiC | 1304169 | c.1239T>C | synonymous_variant | 1.0 |
| fbiC | 1304172 | c.1242G>C | synonymous_variant | 1.0 |
| fbiC | 1304173 | p.Val415Thr | missense_variant | 1.0 |
| fbiC | 1304181 | c.1251G>C | synonymous_variant | 1.0 |
| fbiC | 1304184 | c.1254G>T | synonymous_variant | 1.0 |
| fbiC | 1304199 | c.1269C>G | synonymous_variant | 1.0 |
| fbiC | 1304205 | c.1275C>G | synonymous_variant | 1.0 |
| fbiC | 1304222 | p.Val431Ala | missense_variant | 1.0 |
| fbiC | 1304226 | c.1296C>G | synonymous_variant | 1.0 |
| fbiC | 1304227 | p.Met433Leu | missense_variant | 1.0 |
| fbiC | 1304496 | c.1566T>G | synonymous_variant | 0.75 |
| fbiC | 1304499 | c.1569T>C | synonymous_variant | 1.0 |
| fbiC | 1304502 | c.1572G>A | synonymous_variant | 1.0 |
| fbiC | 1304515 | p.Ala529Thr | missense_variant | 1.0 |
| fbiC | 1304523 | c.1593G>T | synonymous_variant | 1.0 |
| fbiC | 1304526 | c.1596T>C | synonymous_variant | 1.0 |
| fbiC | 1304541 | c.1611C>G | synonymous_variant | 1.0 |
| fbiC | 1304544 | c.1614T>C | synonymous_variant | 1.0 |
| fbiC | 1304545 | p.Val539Thr | missense_variant | 1.0 |
| fbiC | 1304553 | c.1623C>G | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>A | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>G | synonymous_variant | 1.0 |
| fbiC | 1304670 | c.1740G>C | synonymous_variant | 1.0 |
| fbiC | 1304671 | p.Val581Thr | missense_variant | 1.0 |
| fbiC | 1304675 | p.Gly582Glu | missense_variant | 1.0 |
| fbiC | 1304686 | p.Asp586Gln | missense_variant | 1.0 |
| fbiC | 1304691 | c.1761G>C | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>G | synonymous_variant | 1.0 |
| fbiC | 1304710 | p.Ala594Gln | missense_variant | 1.0 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304754 | c.1824G>A | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>C | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>G | synonymous_variant | 1.0 |
| fbiC | 1304808 | c.1878C>G | synonymous_variant | 1.0 |
| fbiC | 1304811 | c.1881C>G | synonymous_variant | 1.0 |
| fbiC | 1304817 | c.1887T>C | synonymous_variant | 1.0 |
| fbiC | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>G | synonymous_variant | 1.0 |
| fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.95 |
| fbiC | 1304874 | c.1944C>T | synonymous_variant | 0.95 |
| fbiC | 1304875 | p.Ile649Val | missense_variant | 0.95 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.97 |
| fbiC | 1304925 | c.1995G>C | synonymous_variant | 0.93 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.93 |
| fbiC | 1304931 | c.2001C>G | synonymous_variant | 0.93 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.94 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.94 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.94 |
| fbiC | 1304958 | c.2028T>C | synonymous_variant | 0.97 |
| fbiC | 1304991 | c.2061G>C | synonymous_variant | 0.92 |
| fbiC | 1304994 | c.2064A>C | synonymous_variant | 0.91 |
| fbiC | 1304995 | p.Leu689Glu | missense_variant | 0.91 |
| fbiC | 1305006 | p.Glu692Asp | missense_variant | 0.91 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.91 |
| fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.84 |
| fbiC | 1305030 | c.2100G>C | synonymous_variant | 0.88 |
| fbiC | 1305033 | c.2103T>C | synonymous_variant | 0.87 |
| fbiC | 1305039 | c.2109G>C | synonymous_variant | 0.87 |
| fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.86 |
| fbiC | 1305045 | c.2115A>G | synonymous_variant | 0.86 |
| fbiC | 1305051 | c.2121G>C | synonymous_variant | 0.82 |
| fbiC | 1305063 | c.2133G>A | synonymous_variant | 0.71 |
| fbiC | 1305113 | p.Asp728Gly | missense_variant | 0.67 |
| fbiC | 1305117 | c.2187T>C | synonymous_variant | 0.67 |
| fbiC | 1305126 | c.2196T>C | synonymous_variant | 1.0 |
| fbiC | 1305154 | c.2224T>C | synonymous_variant | 1.0 |
| fbiC | 1305173 | p.Asn748Ser | missense_variant | 1.0 |
| fbiC | 1305177 | c.2247A>C | synonymous_variant | 1.0 |
| fbiC | 1305181 | c.2251T>C | synonymous_variant | 1.0 |
| fbiC | 1305186 | c.2256C>T | synonymous_variant | 1.0 |
| fbiC | 1305195 | c.2265T>C | synonymous_variant | 1.0 |
| fbiC | 1305198 | c.2268G>C | synonymous_variant | 1.0 |
| fbiC | 1305201 | c.2271G>C | synonymous_variant | 1.0 |
| fbiC | 1305207 | c.2277C>G | synonymous_variant | 1.0 |
| fbiC | 1305213 | c.2283C>G | synonymous_variant | 1.0 |
| fbiC | 1305215 | p.Ser762Thr | missense_variant | 1.0 |
| fbiC | 1305219 | c.2289T>C | synonymous_variant | 1.0 |
| fbiC | 1305231 | c.2301C>G | synonymous_variant | 1.0 |
| fbiC | 1305237 | c.2307A>G | synonymous_variant | 1.0 |
| fbiC | 1305240 | c.2310T>C | synonymous_variant | 1.0 |
| fbiC | 1305243 | c.2313T>G | synonymous_variant | 1.0 |
| fbiC | 1305244 | c.2314T>C | synonymous_variant | 1.0 |
| fbiC | 1305252 | c.2322G>A | synonymous_variant | 1.0 |
| fbiC | 1305276 | c.2346G>C | synonymous_variant | 1.0 |
| fbiC | 1305279 | p.His783Gln | missense_variant | 1.0 |
| fbiC | 1305282 | c.2352T>C | synonymous_variant | 1.0 |
| fbiC | 1305297 | c.2367G>C | synonymous_variant | 1.0 |
| fbiC | 1305300 | c.2370A>G | synonymous_variant | 1.0 |
| fbiC | 1305303 | c.2373T>G | synonymous_variant | 1.0 |
| fbiC | 1305306 | c.2376A>C | synonymous_variant | 1.0 |
| fbiC | 1305309 | c.2379G>C | synonymous_variant | 1.0 |
| fbiC | 1305310 | p.Arg794Glu | missense_variant | 1.0 |
| fbiC | 1305317 | p.Thr796Ser | missense_variant | 1.0 |
| fbiC | 1305320 | p.Gln797Arg | missense_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305336 | c.2406T>C | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>G | synonymous_variant | 0.96 |
| fbiC | 1305399 | c.2469A>G | synonymous_variant | 0.95 |
| fbiC | 1305405 | c.2475A>C | synonymous_variant | 0.95 |
| fbiC | 1305409 | p.Ala827Ser | missense_variant | 0.95 |
| fbiC | 1305422 | p.Ala831Glu | missense_variant | 0.92 |
| fbiC | 1305430 | p.Val834Thr | missense_variant | 0.91 |
| fbiC | 1305442 | p.Glu838Gln | missense_variant | 0.89 |
| fbiC | 1305453 | c.2523C>G | synonymous_variant | 1.0 |
| fbiC | 1305459 | c.2529G>C | synonymous_variant | 1.0 |
| fbiC | 1305465 | c.2535C>G | synonymous_variant | 1.0 |
| Rv1258c | 1406568 | p.Val258Ala | missense_variant | 0.71 |
| Rv1258c | 1406570 | c.771G>C | synonymous_variant | 0.71 |
| Rv1258c | 1406573 | c.768A>G | synonymous_variant | 0.83 |
| Rv1258c | 1406576 | p.Gln255His | missense_variant | 0.83 |
| Rv1258c | 1406579 | p.His254Arg | missense_variant | 0.83 |
| Rv1258c | 1406586 | p.Thr252Ser | missense_variant | 0.86 |
| Rv1258c | 1406594 | c.747A>G | synonymous_variant | 1.0 |
| Rv1258c | 1406618 | c.723G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406624 | c.717T>C | synonymous_variant | 1.0 |
| Rv1258c | 1406627 | c.714G>A | synonymous_variant | 1.0 |
| Rv1258c | 1406630 | c.711G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406636 | c.705C>G | synonymous_variant | 1.0 |
| Rv1258c | 1406641 | p.Thr234Ala | missense_variant | 1.0 |
| embR | 1416631 | c.717C>G | synonymous_variant | 1.0 |
| embR | 1416635 | p.Asp238Gly | missense_variant | 1.0 |
| embR | 1416646 | p.Thr234Ala | missense_variant | 1.0 |
| embR | 1416649 | c.699A>C | synonymous_variant | 1.0 |
| embR | 1416657 | p.Val231Leu | missense_variant | 1.0 |
| embR | 1416661 | c.687C>T | synonymous_variant | 1.0 |
| embR | 1416664 | p.Tyr228Phe | missense_variant | 1.0 |
| embR | 1416673 | c.675G>C | synonymous_variant | 1.0 |
| embR | 1416679 | c.669T>C | synonymous_variant | 1.0 |
| embR | 1416688 | c.660G>C | synonymous_variant | 1.0 |
| embR | 1416691 | p.Asp219Glu | missense_variant | 1.0 |
| embR | 1416696 | p.Ser218Thr | missense_variant | 1.0 |
| embR | 1416699 | p.Leu217Val | missense_variant | 1.0 |
| embR | 1416721 | p.Thr209Ala | missense_variant | 1.0 |
| embR | 1416733 | c.615G>A | synonymous_variant | 1.0 |
| embR | 1416739 | c.609C>T | synonymous_variant | 1.0 |
| embR | 1416742 | c.606C>G | synonymous_variant | 1.0 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 1.0 |
| atpE | 1460855 | c.-190T>C | upstream_gene_variant | 1.0 |
| atpE | 1460858 | c.-187C>G | upstream_gene_variant | 1.0 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1460894 | c.-151A>G | upstream_gene_variant | 1.0 |
| atpE | 1460897 | c.-148A>G | upstream_gene_variant | 1.0 |
| atpE | 1460900 | c.-145T>C | upstream_gene_variant | 1.0 |
| atpE | 1460918 | c.-127A>C | upstream_gene_variant | 1.0 |
| atpE | 1460933 | c.-112T>C | upstream_gene_variant | 1.0 |
| atpE | 1461089 | c.45G>C | synonymous_variant | 1.0 |
| atpE | 1461097 | p.Ala18Gly | missense_variant | 1.0 |
| atpE | 1461101 | c.57T>C | synonymous_variant | 1.0 |
| atpE | 1461107 | c.63C>G | synonymous_variant | 1.0 |
| atpE | 1461113 | c.69C>T | synonymous_variant | 1.0 |
| atpE | 1461131 | c.87T>C | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461150 | p.Ile36Val | missense_variant | 1.0 |
| atpE | 1461153 | p.Ser37Ala | missense_variant | 1.0 |
| atpE | 1461158 | c.114T>C | synonymous_variant | 1.0 |
| atpE | 1461159 | p.Val39Ile | missense_variant | 0.97 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461269 | c.225C>G | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>C | synonymous_variant | 1.0 |
| atpE | 1461281 | c.237C>G | synonymous_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472445 | n.601_604delTCTC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472451 | n.606_607insCGGG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472463 | n.618G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473408 | n.-250C>T | upstream_gene_variant | 1.0 |
| rrl | 1473417 | n.-241C>T | upstream_gene_variant | 1.0 |
| rrl | 1473419 | n.-239T>C | upstream_gene_variant | 1.0 |
| rrl | 1473421 | n.-237G>A | upstream_gene_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474999 | n.1342C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475366 | n.1709G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475401 | n.1745delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475405 | n.1748A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476792 | n.3135A>C | non_coding_transcript_exon_variant | 0.67 |
| inhA | 1673571 | c.-631C>T | upstream_gene_variant | 0.5 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.5 |
| inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.67 |
| inhA | 1673589 | c.-613A>C | upstream_gene_variant | 0.67 |
| inhA | 1673592 | c.-610G>A | upstream_gene_variant | 0.67 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 0.67 |
| fabG1 | 1673596 | p.Lys53Glu | missense_variant | 0.67 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 0.67 |
| inhA | 1673610 | c.-592C>T | upstream_gene_variant | 0.67 |
| fabG1 | 1673615 | p.Glu59Val | missense_variant | 0.75 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 0.75 |
| inhA | 1673646 | c.-556T>C | upstream_gene_variant | 0.8 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 0.75 |
| inhA | 1673660 | c.-542C>A | upstream_gene_variant | 0.67 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 0.67 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 0.67 |
| inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.75 |
| inhA | 1673685 | c.-517C>G | upstream_gene_variant | 0.78 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.71 |
| inhA | 1673715 | c.-487C>G | upstream_gene_variant | 0.6 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 0.6 |
| inhA | 1673724 | c.-478A>G | upstream_gene_variant | 0.75 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 0.75 |
| inhA | 1673796 | c.-406G>A | upstream_gene_variant | 1.0 |
| inhA | 1673799 | c.-403T>C | upstream_gene_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673808 | c.-394A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673829 | p.Asn130Lys | missense_variant | 1.0 |
| fabG1 | 1673830 | p.Lys131Arg | missense_variant | 1.0 |
| inhA | 1673838 | c.-364T>C | upstream_gene_variant | 1.0 |
| inhA | 1673841 | c.-361A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673844 | p.Met135Ile | missense_variant | 1.0 |
| inhA | 1673847 | c.-355A>C | upstream_gene_variant | 1.0 |
| inhA | 1673853 | c.-349A>T | upstream_gene_variant | 1.0 |
| inhA | 1673862 | c.-340C>A | upstream_gene_variant | 1.0 |
| inhA | 1673865 | c.-337C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673870 | p.Ser144Met | missense_variant | 1.0 |
| inhA | 1673883 | c.-319C>G | upstream_gene_variant | 1.0 |
| inhA | 1673892 | c.-310C>G | upstream_gene_variant | 1.0 |
| inhA | 1673901 | c.-301A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674084 | c.647_649dupAGG | disruptive_inframe_insertion | 1.0 |
| fabG1 | 1674098 | p.Val220Ala | missense_variant | 1.0 |
| inhA | 1674114 | c.-88T>G | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>C | upstream_gene_variant | 1.0 |
| inhA | 1674129 | c.-73C>T | upstream_gene_variant | 1.0 |
| inhA | 1674132 | c.-70T>C | upstream_gene_variant | 1.0 |
| inhA | 1674135 | c.-67C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1674136 | p.Ser233Ala | missense_variant | 1.0 |
| inhA | 1674141 | c.-61T>C | upstream_gene_variant | 1.0 |
| inhA | 1674144 | c.-58G>C | upstream_gene_variant | 1.0 |
| inhA | 1674171 | c.-31T>C | upstream_gene_variant | 1.0 |
| inhA | 1674199 | c.-3C>G | upstream_gene_variant | 1.0 |
| inhA | 1674205 | p.Thr2Ala | missense_variant | 1.0 |
| inhA | 1674216 | c.15G>C | synonymous_variant | 1.0 |
| inhA | 1674228 | c.27G>A | synonymous_variant | 1.0 |
| inhA | 1674231 | c.30T>C | synonymous_variant | 1.0 |
| inhA | 1674237 | c.36T>C | synonymous_variant | 1.0 |
| inhA | 1674243 | c.42A>C | synonymous_variant | 1.0 |
| inhA | 1674270 | c.69T>C | synonymous_variant | 1.0 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 1.0 |
| inhA | 1674280 | p.Arg27Lys | missense_variant | 1.0 |
| inhA | 1674285 | c.84A>G | synonymous_variant | 1.0 |
| inhA | 1674294 | c.93G>A | synonymous_variant | 1.0 |
| inhA | 1674295 | p.Gln32Ala | missense_variant | 1.0 |
| inhA | 1674300 | c.99C>A | synonymous_variant | 1.0 |
| inhA | 1674306 | c.105G>A | synonymous_variant | 1.0 |
| inhA | 1674315 | c.114C>G | synonymous_variant | 1.0 |
| inhA | 1674318 | c.117C>A | synonymous_variant | 1.0 |
| inhA | 1674331 | c.130C>T | synonymous_variant | 1.0 |
| inhA | 1674336 | c.135G>A | synonymous_variant | 1.0 |
| inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
| inhA | 1674456 | c.255C>T | synonymous_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674489 | c.288G>C | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674540 | c.339C>T | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674570 | c.369G>T | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674601 | c.400C>T | synonymous_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 1.0 |
| inhA | 1674654 | c.453G>C | synonymous_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674663 | c.462G>C | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674714 | c.513C>G | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517_519delAGGinsCGC | synonymous_variant | 1.0 |
| inhA | 1674726 | c.525G>C | synonymous_variant | 1.0 |
| inhA | 1674729 | c.528G>A | synonymous_variant | 1.0 |
| inhA | 1674747 | c.546C>T | synonymous_variant | 0.94 |
| inhA | 1674750 | c.549T>C | synonymous_variant | 0.97 |
| inhA | 1674756 | c.555T>C | synonymous_variant | 0.93 |
| inhA | 1674762 | c.561T>C | synonymous_variant | 0.97 |
| inhA | 1674765 | c.564C>T | synonymous_variant | 0.96 |
| inhA | 1674774 | c.573A>C | synonymous_variant | 0.96 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 0.97 |
| inhA | 1674795 | c.594G>C | synonymous_variant | 0.97 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 0.97 |
| inhA | 1674813 | c.612C>T | synonymous_variant | 0.97 |
| inhA | 1674837 | c.636C>G | synonymous_variant | 0.95 |
| inhA | 1674840 | c.639C>G | synonymous_variant | 0.94 |
| inhA | 1674846 | p.Ile215Met | missense_variant | 0.97 |
| inhA | 1674855 | c.654C>G | synonymous_variant | 0.97 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 0.96 |
| inhA | 1674873 | c.672G>A | synonymous_variant | 0.96 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 0.95 |
| inhA | 1674888 | c.687C>T | synonymous_variant | 0.88 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 0.6 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833613 | c.72C>A | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833622 | c.81C>T | synonymous_variant | 1.0 |
| rpsA | 1833634 | c.93G>A | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833754 | c.213G>A | synonymous_variant | 1.0 |
| rpsA | 1833771 | p.Asn77Ser | missense_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833806 | c.265C>T | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 0.98 |
| rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834120 | c.579G>A | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 1.0 |
| rpsA | 1834153 | c.612T>C | synonymous_variant | 1.0 |
| rpsA | 1834154 | p.Asn205Gln | missense_variant | 1.0 |
| rpsA | 1834157 | c.616T>C | synonymous_variant | 1.0 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834192 | c.651C>G | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834255 | c.714C>G | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 0.99 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 0.99 |
| rpsA | 1834327 | c.786G>C | synonymous_variant | 0.97 |
| rpsA | 1834336 | c.795C>G | synonymous_variant | 0.97 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 0.96 |
| rpsA | 1834357 | c.816T>C | synonymous_variant | 0.96 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 0.96 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 0.95 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 0.94 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 0.96 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 0.96 |
| rpsA | 1834423 | c.882G>T | synonymous_variant | 0.97 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 0.98 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 0.98 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 0.98 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 0.98 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 0.98 |
| rpsA | 1834528 | c.987T>G | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>T | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>A | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834699 | p.Glu386Asp | missense_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | c.1224A>G | synonymous_variant | 1.0 |
| rpsA | 1834774 | c.1233C>G | synonymous_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>G | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834831 | c.1290G>C | synonymous_variant | 1.0 |
| tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 0.5 |
| tlyA | 1917940 | p.Val1Met | missense_variant | 0.5 |
| tlyA | 1917943 | p.Ala2Ser | missense_variant | 0.5 |
| tlyA | 1917960 | c.21T>C | synonymous_variant | 0.87 |
| tlyA | 1917969 | c.30G>A | synonymous_variant | 0.87 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 0.86 |
| tlyA | 1917984 | c.45C>G | synonymous_variant | 0.86 |
| tlyA | 1917990 | c.51G>C | synonymous_variant | 0.86 |
| tlyA | 1917993 | c.54A>G | synonymous_variant | 0.86 |
| tlyA | 1917996 | c.57A>C | synonymous_variant | 0.86 |
| tlyA | 1917999 | c.60T>G | synonymous_variant | 0.86 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 0.86 |
| tlyA | 1918022 | p.Gly28Asp | missense_variant | 1.0 |
| tlyA | 1918031 | p.Lys31Arg | missense_variant | 1.0 |
| tlyA | 1918035 | c.96G>C | synonymous_variant | 1.0 |
| tlyA | 1918036 | p.Arg33Ser | missense_variant | 1.0 |
| tlyA | 1918047 | c.108G>C | synonymous_variant | 0.8 |
| tlyA | 1918387 | p.Leu150Val | missense_variant | 1.0 |
| tlyA | 1918392 | c.453A>G | synonymous_variant | 1.0 |
| tlyA | 1918395 | c.456G>C | synonymous_variant | 1.0 |
| tlyA | 1918417 | c.478T>C | synonymous_variant | 1.0 |
| tlyA | 1918422 | c.483T>C | synonymous_variant | 1.0 |
| tlyA | 1918425 | c.486C>A | synonymous_variant | 1.0 |
| tlyA | 1918442 | p.Val168Ala | missense_variant | 1.0 |
| tlyA | 1918446 | c.507A>C | synonymous_variant | 1.0 |
| tlyA | 1918452 | c.513T>C | synonymous_variant | 1.0 |
| tlyA | 1918453 | p.Ser172Ala | missense_variant | 1.0 |
| tlyA | 1918457 | p.Arg173Pro | missense_variant | 1.0 |
| tlyA | 1918464 | c.525C>G | synonymous_variant | 1.0 |
| tlyA | 1918476 | c.537A>C | synonymous_variant | 1.0 |
| tlyA | 1918477 | p.Leu180Met | missense_variant | 1.0 |
| tlyA | 1918488 | c.549G>A | synonymous_variant | 1.0 |
| ndh | 2101858 | p.Ile395Met | missense_variant | 1.0 |
| ndh | 2101863 | c.1180C>T | synonymous_variant | 1.0 |
| ndh | 2101873 | c.1170T>C | synonymous_variant | 1.0 |
| ndh | 2101876 | c.1167C>G | synonymous_variant | 1.0 |
| ndh | 2101888 | p.Val385Leu | missense_variant | 1.0 |
| ndh | 2101891 | c.1152C>G | synonymous_variant | 1.0 |
| ndh | 2101894 | c.1149T>G | synonymous_variant | 1.0 |
| ndh | 2101912 | c.1131G>C | synonymous_variant | 1.0 |
| ndh | 2101915 | c.1128T>C | synonymous_variant | 1.0 |
| ndh | 2101920 | c.1123A>C | synonymous_variant | 1.0 |
| ndh | 2101924 | c.1119T>G | synonymous_variant | 1.0 |
| ndh | 2101930 | c.1113C>T | synonymous_variant | 1.0 |
| ndh | 2101939 | c.1104A>G | synonymous_variant | 1.0 |
| ndh | 2101960 | c.1083A>G | synonymous_variant | 1.0 |
| ndh | 2101966 | c.1077T>C | synonymous_variant | 1.0 |
| ndh | 2102787 | c.256T>C | synonymous_variant | 1.0 |
| ndh | 2102791 | c.252A>G | synonymous_variant | 1.0 |
| ndh | 2102800 | c.243T>C | synonymous_variant | 1.0 |
| ndh | 2102809 | p.Lys78His | missense_variant | 1.0 |
| ndh | 2102812 | c.231T>G | synonymous_variant | 1.0 |
| ndh | 2102821 | c.222C>G | synonymous_variant | 1.0 |
| ndh | 2102830 | p.Pro71Ala | missense_variant | 1.0 |
| ndh | 2102833 | c.210G>C | synonymous_variant | 1.0 |
| ndh | 2102836 | c.207T>C | synonymous_variant | 1.0 |
| ndh | 2102842 | c.201A>G | synonymous_variant | 1.0 |
| ndh | 2102845 | c.198A>C | synonymous_variant | 1.0 |
| ndh | 2102857 | c.186T>C | synonymous_variant | 1.0 |
| ndh | 2102878 | c.165G>C | synonymous_variant | 1.0 |
| ndh | 2102905 | c.138C>G | synonymous_variant | 1.0 |
| ndh | 2102911 | c.132G>C | synonymous_variant | 0.93 |
| ndh | 2102929 | c.114T>C | synonymous_variant | 0.93 |
| ndh | 2102934 | p.Asp37Asn | missense_variant | 0.93 |
| ndh | 2102938 | p.Arg35His | missense_variant | 0.92 |
| ndh | 2102947 | c.96G>A | synonymous_variant | 0.91 |
| ndh | 2102953 | c.90A>G | synonymous_variant | 0.9 |
| ndh | 2102962 | c.81A>C | synonymous_variant | 0.75 |
| ndh | 2102965 | c.78G>T | synonymous_variant | 0.75 |
| ndh | 2102968 | c.75C>T | synonymous_variant | 0.75 |
| ndh | 2102974 | c.69G>A | synonymous_variant | 0.67 |
| ndh | 2102977 | c.66T>G | synonymous_variant | 0.67 |
| katG | 2155017 | c.1095G>C | synonymous_variant | 1.0 |
| katG | 2155029 | c.1083C>G | synonymous_variant | 1.0 |
| katG | 2155032 | c.1080T>C | synonymous_variant | 1.0 |
| katG | 2155050 | p.Thr354Gln | missense_variant | 1.0 |
| katG | 2155054 | p.Tyr353Phe | missense_variant | 1.0 |
| katG | 2155056 | c.1056A>G | synonymous_variant | 1.0 |
| katG | 2155062 | c.1050T>G | synonymous_variant | 1.0 |
| katG | 2155065 | c.1047C>G | synonymous_variant | 1.0 |
| katG | 2155068 | c.1044T>C | synonymous_variant | 1.0 |
| katG | 2155071 | c.1041T>G | synonymous_variant | 1.0 |
| katG | 2155080 | c.1032G>C | synonymous_variant | 1.0 |
| katG | 2155104 | c.1008G>C | synonymous_variant | 1.0 |
| katG | 2155108 | p.Ile335Asn | missense_variant | 1.0 |
| katG | 2155649 | p.Tyr155His | missense_variant | 1.0 |
| katG | 2155655 | p.Lys153Gln | missense_variant | 1.0 |
| katG | 2155659 | c.453C>G | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155698 | c.414C>T | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155736 | p.Met126Leu | missense_variant | 1.0 |
| katG | 2155740 | p.Gly124Gln | missense_variant | 1.0 |
| katG | 2155743 | c.369G>T | synonymous_variant | 1.0 |
| katG | 2155747 | p.Ala122Gly | missense_variant | 1.0 |
| katG | 2155766 | p.His116Tyr | missense_variant | 1.0 |
| katG | 2155770 | c.342C>G | synonymous_variant | 1.0 |
| pncA | 2289988 | c.-747G>C | upstream_gene_variant | 1.0 |
| pncA | 2289991 | c.-750G>C | upstream_gene_variant | 1.0 |
| pncA | 2289994 | c.-753A>G | upstream_gene_variant | 1.0 |
| pncA | 2289997 | c.-756G>C | upstream_gene_variant | 1.0 |
| pncA | 2290001 | c.-760A>T | upstream_gene_variant | 1.0 |
| pncA | 2290006 | c.-765T>C | upstream_gene_variant | 1.0 |
| pncA | 2290009 | c.-768A>G | upstream_gene_variant | 1.0 |
| pncA | 2290015 | c.-774A>C | upstream_gene_variant | 1.0 |
| pncA | 2290018 | c.-777C>T | upstream_gene_variant | 1.0 |
| pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 1.0 |
| pncA | 2290042 | c.-801T>G | upstream_gene_variant | 1.0 |
| pncA | 2290066 | c.-825G>C | upstream_gene_variant | 1.0 |
| pncA | 2290072 | c.-831T>C | upstream_gene_variant | 1.0 |
| pncA | 2290075 | c.-834C>G | upstream_gene_variant | 1.0 |
| pncA | 2290084 | c.-843T>C | upstream_gene_variant | 1.0 |
| pncA | 2290087 | c.-846T>C | upstream_gene_variant | 1.0 |
| kasA | 2517950 | c.-165C>G | upstream_gene_variant | 1.0 |
| kasA | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
| kasA | 2517968 | c.-147T>C | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>G | upstream_gene_variant | 0.97 |
| kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.97 |
| kasA | 2517993 | c.-122G>T | upstream_gene_variant | 1.0 |
| kasA | 2518019 | c.-96A>G | upstream_gene_variant | 1.0 |
| kasA | 2518025 | c.-90G>C | upstream_gene_variant | 1.0 |
| kasA | 2518031 | c.-84G>T | upstream_gene_variant | 1.0 |
| kasA | 2518034 | c.-81T>C | upstream_gene_variant | 1.0 |
| kasA | 2518035 | c.-80C>G | upstream_gene_variant | 1.0 |
| kasA | 2518041 | c.-74T>C | upstream_gene_variant | 1.0 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 1.0 |
| kasA | 2518053 | c.-62_-60delATTinsCTG | upstream_gene_variant | 1.0 |
| kasA | 2518059 | c.-56T>A | upstream_gene_variant | 1.0 |
| kasA | 2518064 | c.-51G>C | upstream_gene_variant | 1.0 |
| kasA | 2518073 | c.-42T>G | upstream_gene_variant | 1.0 |
| kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
| kasA | 2518138 | c.24T>C | synonymous_variant | 0.86 |
| kasA | 2518146 | p.Phe11Tyr | missense_variant | 0.88 |
| kasA | 2518152 | p.Ser13Asn | missense_variant | 0.94 |
| kasA | 2518162 | c.48G>A | synonymous_variant | 0.92 |
| kasA | 2518168 | c.54C>T | synonymous_variant | 0.96 |
| kasA | 2518172 | p.Thr20Ala | missense_variant | 0.96 |
| kasA | 2518177 | c.63G>A | synonymous_variant | 0.97 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 0.97 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 0.97 |
| kasA | 2518223 | c.109T>C | synonymous_variant | 0.97 |
| kasA | 2518231 | c.117C>G | synonymous_variant | 0.96 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 0.96 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 0.94 |
| kasA | 2518265 | p.Val51Ile | missense_variant | 1.0 |
| kasA | 2518279 | p.Asp55Glu | missense_variant | 1.0 |
| kasA | 2518282 | c.168A>G | synonymous_variant | 1.0 |
| kasA | 2518283 | p.Ala57Pro | missense_variant | 1.0 |
| kasA | 2518288 | c.174C>G | synonymous_variant | 1.0 |
| kasA | 2518289 | p.Lys59Gln | missense_variant | 1.0 |
| kasA | 2518300 | c.186T>C | synonymous_variant | 1.0 |
| kasA | 2518312 | p.Asp66Glu | missense_variant | 1.0 |
| kasA | 2518316 | p.Val68Ile | missense_variant | 1.0 |
| kasA | 2518322 | p.Ser70Glu | missense_variant | 1.0 |
| kasA | 2518336 | c.222A>G | synonymous_variant | 1.0 |
| kasA | 2518343 | p.Met77Leu | missense_variant | 1.0 |
| kasA | 2518459 | c.345T>G | synonymous_variant | 1.0 |
| kasA | 2518462 | c.348A>C | synonymous_variant | 1.0 |
| kasA | 2518465 | c.351T>C | synonymous_variant | 0.8 |
| kasA | 2518468 | c.354A>C | synonymous_variant | 1.0 |
| kasA | 2518475 | c.361A>C | synonymous_variant | 1.0 |
| kasA | 2518480 | c.366T>C | synonymous_variant | 1.0 |
| kasA | 2518483 | c.369C>G | synonymous_variant | 1.0 |
| kasA | 2518504 | c.390T>C | synonymous_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 0.96 |
| kasA | 2518528 | c.414C>G | synonymous_variant | 0.96 |
| kasA | 2518534 | c.420G>C | synonymous_variant | 0.96 |
| kasA | 2518561 | c.447T>C | synonymous_variant | 0.92 |
| kasA | 2518573 | c.459G>C | synonymous_variant | 0.9 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 0.9 |
| kasA | 2518579 | c.465T>C | synonymous_variant | 0.9 |
| kasA | 2518585 | c.471G>A | synonymous_variant | 0.88 |
| kasA | 2518588 | c.474T>G | synonymous_variant | 0.88 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 0.88 |
| kasA | 2518609 | p.Met165Ile | missense_variant | 0.88 |
| kasA | 2518612 | c.498C>T | synonymous_variant | 0.85 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 0.86 |
| kasA | 2518627 | c.513T>C | synonymous_variant | 0.86 |
| kasA | 2518633 | c.519G>C | synonymous_variant | 0.87 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 0.89 |
| kasA | 2518651 | c.537C>G | synonymous_variant | 0.89 |
| kasA | 2518663 | c.549T>C | synonymous_variant | 0.94 |
| kasA | 2518666 | c.552G>A | synonymous_variant | 0.94 |
| kasA | 2518671 | p.Val186Ala | missense_variant | 0.94 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 0.96 |
| kasA | 2518687 | c.573C>T | synonymous_variant | 0.98 |
| kasA | 2518688 | p.Val192Phe | missense_variant | 0.98 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 0.98 |
| kasA | 2518714 | c.600A>T | synonymous_variant | 1.0 |
| kasA | 2518717 | c.603C>G | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518759 | c.645C>G | synonymous_variant | 1.0 |
| kasA | 2518765 | c.651G>C | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518789 | c.675G>C | synonymous_variant | 1.0 |
| kasA | 2518792 | c.678C>G | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
| kasA | 2518807 | c.693C>T | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518834 | c.720C>T | synonymous_variant | 1.0 |
| kasA | 2518837 | c.723G>A | synonymous_variant | 1.0 |
| kasA | 2518853 | p.Leu247Ile | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518867 | c.753G>A | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| kasA | 2518882 | c.768C>T | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2519095 | c.981C>G | synonymous_variant | 0.67 |
| kasA | 2519098 | c.984C>T | synonymous_variant | 0.67 |
| kasA | 2519104 | c.990T>A | synonymous_variant | 1.0 |
| kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
| kasA | 2519111 | p.Gln333Asp | missense_variant | 1.0 |
| kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
| kasA | 2519128 | c.1014G>A | synonymous_variant | 1.0 |
| kasA | 2519137 | c.1023T>C | synonymous_variant | 1.0 |
| kasA | 2519140 | c.1026G>A | synonymous_variant | 1.0 |
| kasA | 2519146 | c.1032C>G | synonymous_variant | 1.0 |
| kasA | 2519158 | c.1044C>T | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>G | synonymous_variant | 1.0 |
| kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
| kasA | 2519182 | c.1068G>C | synonymous_variant | 1.0 |
| kasA | 2519196 | p.Thr361Ser | missense_variant | 1.0 |
| kasA | 2519203 | c.1089C>G | synonymous_variant | 1.0 |
| kasA | 2519218 | c.1104G>C | synonymous_variant | 1.0 |
| kasA | 2519224 | c.1110C>G | synonymous_variant | 0.97 |
| kasA | 2519239 | c.1125A>C | synonymous_variant | 0.98 |
| kasA | 2519260 | c.1146T>G | synonymous_variant | 0.97 |
| kasA | 2519263 | c.1149C>T | synonymous_variant | 0.97 |
| kasA | 2519266 | c.1152C>G | synonymous_variant | 0.97 |
| kasA | 2519269 | c.1155C>T | synonymous_variant | 0.97 |
| kasA | 2519272 | c.1158C>G | synonymous_variant | 0.97 |
| kasA | 2519281 | c.1167G>T | synonymous_variant | 0.98 |
| kasA | 2519287 | c.1173T>C | synonymous_variant | 0.98 |
| kasA | 2519295 | p.Tyr394Phe | missense_variant | 0.98 |
| kasA | 2519299 | c.1185C>T | synonymous_variant | 0.98 |
| kasA | 2519306 | p.Val398Ile | missense_variant | 0.98 |
| kasA | 2519329 | c.1215C>A | synonymous_variant | 0.91 |
| kasA | 2519338 | c.1224T>C | synonymous_variant | 0.89 |
| kasA | 2519347 | c.1233T>C | synonymous_variant | 0.84 |
| kasA | 2519359 | c.1245T>C | synonymous_variant | 0.82 |
| ahpC | 2726204 | c.12A>G | synonymous_variant | 1.0 |
| ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
| ahpC | 2726216 | c.24T>C | synonymous_variant | 1.0 |
| ahpC | 2726219 | c.27A>G | synonymous_variant | 1.0 |
| ahpC | 2726232 | p.Gln14Glu | missense_variant | 1.0 |
| ahpC | 2726243 | c.51T>G | synonymous_variant | 1.0 |
| ahpC | 2726251 | p.Gly20Ala | missense_variant | 1.0 |
| ahpC | 2726258 | c.66C>T | synonymous_variant | 1.0 |
| ahpC | 2726287 | p.Gly32Glu | missense_variant | 1.0 |
| ahpC | 2726575 | p.Asp128Gly | missense_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
| ahpC | 2726591 | c.399C>G | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726636 | c.444G>C | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726642 | c.450C>G | synonymous_variant | 1.0 |
| ahpC | 2726651 | c.459G>C | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | p.Asp159Glu | missense_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726684 | c.492G>C | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726699 | c.507G>A | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>C | synonymous_variant | 1.0 |
| folC | 2746264 | p.Ser445Ala | missense_variant | 1.0 |
| folC | 2746270 | c.1329C>G | synonymous_variant | 1.0 |
| folC | 2746273 | c.1326T>G | synonymous_variant | 1.0 |
| folC | 2746282 | c.1317T>C | synonymous_variant | 1.0 |
| folC | 2746285 | c.1314T>C | synonymous_variant | 1.0 |
| folC | 2746308 | p.Arg431Ser | missense_variant | 1.0 |
| folC | 2746309 | c.1290G>C | synonymous_variant | 1.0 |
| folC | 2746315 | p.Asp428Glu | missense_variant | 1.0 |
| folC | 2746321 | c.1278A>C | synonymous_variant | 1.0 |
| folC | 2746327 | c.1272G>C | synonymous_variant | 1.0 |
| folC | 2746331 | p.Glu423Ala | missense_variant | 1.0 |
| folC | 2746333 | p.Gly422Ala | missense_variant | 1.0 |
| folC | 2746344 | p.Leu419Val | missense_variant | 1.0 |
| folC | 2746346 | p.Ala418Gly | missense_variant | 1.0 |
| folC | 2746351 | c.1248C>G | synonymous_variant | 1.0 |
| folC | 2746360 | c.1239T>C | synonymous_variant | 1.0 |
| folC | 2746372 | c.1227G>C | synonymous_variant | 1.0 |
| folC | 2746375 | c.1224G>A | synonymous_variant | 1.0 |
| folC | 2746384 | c.1215C>T | synonymous_variant | 1.0 |
| folC | 2746396 | c.1203C>G | synonymous_variant | 1.0 |
| folC | 2746399 | p.Ser400Ala | missense_variant | 1.0 |
| folC | 2746402 | c.1197T>C | synonymous_variant | 1.0 |
| folC | 2746408 | c.1191G>C | synonymous_variant | 1.0 |
| folC | 2746414 | c.1185G>A | synonymous_variant | 1.0 |
| folC | 2746420 | c.1179A>G | synonymous_variant | 1.0 |
| folC | 2746426 | c.1173G>C | synonymous_variant | 1.0 |
| folC | 2746429 | c.1170C>T | synonymous_variant | 1.0 |
| folC | 2746438 | c.1161G>C | synonymous_variant | 1.0 |
| folC | 2747040 | p.Ile187Val | missense_variant | 1.0 |
| folC | 2747059 | c.540T>C | synonymous_variant | 1.0 |
| folC | 2747062 | c.537A>G | synonymous_variant | 1.0 |
| folC | 2747074 | c.525G>C | synonymous_variant | 1.0 |
| folC | 2747083 | c.516G>C | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>C | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>T | synonymous_variant | 1.0 |
| folC | 2747107 | c.492G>C | synonymous_variant | 1.0 |
| folC | 2747110 | c.489T>C | synonymous_variant | 1.0 |
| folC | 2747113 | c.486C>G | synonymous_variant | 1.0 |
| folC | 2747122 | c.477G>C | synonymous_variant | 1.0 |
| folC | 2747137 | c.462G>C | synonymous_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747281 | c.318A>G | synonymous_variant | 1.0 |
| folC | 2747289 | p.Pro104Ala | missense_variant | 1.0 |
| folC | 2747290 | c.309A>G | synonymous_variant | 1.0 |
| folC | 2747302 | c.297A>G | synonymous_variant | 1.0 |
| folC | 2747314 | c.285A>C | synonymous_variant | 0.9 |
| folC | 2747329 | c.270C>T | synonymous_variant | 0.95 |
| folC | 2747334 | c.265C>T | synonymous_variant | 0.95 |
| folC | 2747371 | c.228C>G | synonymous_variant | 0.97 |
| folC | 2747374 | c.225G>A | synonymous_variant | 0.97 |
| folC | 2747389 | c.210G>C | synonymous_variant | 0.97 |
| folC | 2747395 | c.204T>C | synonymous_variant | 0.97 |
| folC | 2747410 | p.Ser63Gly | missense_variant | 1.0 |
| folC | 2747413 | c.186C>G | synonymous_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747439 | p.Met54Leu | missense_variant | 1.0 |
| folC | 2747442 | p.Leu53Val | missense_variant | 1.0 |
| folC | 2747447 | p.Ser51Asn | missense_variant | 1.0 |
| folC | 2747452 | c.147G>C | synonymous_variant | 1.0 |
| folC | 2747467 | p.Asp44Glu | missense_variant | 1.0 |
| folC | 2747473 | p.Arg42Lys | missense_variant | 1.0 |
| folC | 2747491 | c.108A>G | synonymous_variant | 1.0 |
| folC | 2747497 | c.102C>G | synonymous_variant | 1.0 |
| folC | 2747500 | c.99A>G | synonymous_variant | 1.0 |
| folC | 2747503 | c.96T>C | synonymous_variant | 1.0 |
| folC | 2747509 | c.90T>C | synonymous_variant | 1.0 |
| folC | 2747517 | c.82C>T | synonymous_variant | 1.0 |
| folC | 2747521 | c.78C>G | synonymous_variant | 1.0 |
| folC | 2747530 | c.69G>A | synonymous_variant | 1.0 |
| folC | 2747539 | c.60T>C | synonymous_variant | 1.0 |
| folC | 2747700 | c.-102T>C | upstream_gene_variant | 1.0 |
| folC | 2747707 | c.-109C>A | upstream_gene_variant | 1.0 |
| folC | 2747717 | c.-119T>C | upstream_gene_variant | 1.0 |
| folC | 2747718 | c.-120G>A | upstream_gene_variant | 1.0 |
| folC | 2747726 | c.-128G>A | upstream_gene_variant | 1.0 |
| folC | 2747745 | c.-147A>C | upstream_gene_variant | 1.0 |
| folC | 2747748 | c.-150C>G | upstream_gene_variant | 1.0 |
| folC | 2747752 | c.-155_-154delGGinsAT | upstream_gene_variant | 1.0 |
| folC | 2747759 | c.-161T>C | upstream_gene_variant | 1.0 |
| folC | 2747760 | c.-162G>C | upstream_gene_variant | 1.0 |
| folC | 2747766 | c.-168A>G | upstream_gene_variant | 1.0 |
| folC | 2747778 | c.-180T>G | upstream_gene_variant | 1.0 |
| folC | 2747790 | c.-192G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860233 | c.186T>C | synonymous_variant | 1.0 |
| pepQ | 2860242 | c.177G>C | synonymous_variant | 1.0 |
| pepQ | 2860264 | p.Ala52Asp | missense_variant | 1.0 |
| pepQ | 2860266 | p.Asp51Gly | missense_variant | 1.0 |
| pepQ | 2860272 | p.Glu49Asp | missense_variant | 1.0 |
| pepQ | 2860275 | c.144T>C | synonymous_variant | 1.0 |
| pepQ | 2860293 | c.126A>G | synonymous_variant | 1.0 |
| pepQ | 2860305 | c.114G>C | synonymous_variant | 1.0 |
| pepQ | 2860309 | p.Ser37Thr | missense_variant | 1.0 |
| pepQ | 2860389 | c.30G>C | synonymous_variant | 1.0 |
| pepQ | 2860407 | c.12C>A | synonymous_variant | 1.0 |
| pepQ | 2860420 | c.-2T>C | upstream_gene_variant | 1.0 |
| pepQ | 2860421 | c.-3G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860422 | c.-4G>A | upstream_gene_variant | 1.0 |
| pepQ | 2860444 | c.-26C>A | upstream_gene_variant | 1.0 |
| pepQ | 2860445 | c.-27T>A | upstream_gene_variant | 1.0 |
| pepQ | 2860446 | c.-28T>C | upstream_gene_variant | 1.0 |
| pepQ | 2860447 | c.-29A>C | upstream_gene_variant | 1.0 |
| pepQ | 2860456 | c.-38G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3064761 | c.1431C>G | synonymous_variant | 0.67 |
| Rv2752c | 3064764 | c.1428C>G | synonymous_variant | 0.78 |
| Rv2752c | 3064776 | c.1416T>C | synonymous_variant | 0.88 |
| Rv2752c | 3064790 | c.1402T>C | synonymous_variant | 0.89 |
| Rv2752c | 3064791 | c.1401T>C | synonymous_variant | 0.89 |
| Rv2752c | 3064803 | c.1389C>G | synonymous_variant | 0.89 |
| Rv2752c | 3064809 | c.1383C>G | synonymous_variant | 0.89 |
| Rv2752c | 3064815 | c.1377T>C | synonymous_variant | 0.95 |
| Rv2752c | 3064831 | p.Ala454Asp | missense_variant | 1.0 |
| Rv2752c | 3064835 | p.Ile453Val | missense_variant | 1.0 |
| Rv2752c | 3064857 | c.1335C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064869 | c.1323G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064901 | c.1291C>T | synonymous_variant | 1.0 |
| Rv2752c | 3064914 | c.1278T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064923 | c.1269C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064935 | c.1257A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064941 | p.Gln417Glu | missense_variant | 1.0 |
| Rv2752c | 3064947 | c.1245A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 1.0 |
| Rv2752c | 3064959 | c.1233C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064962 | c.1230C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064965 | c.1227G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065022 | c.1170G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065031 | c.1161G>T | synonymous_variant | 1.0 |
| Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065070 | c.1122C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 1.0 |
| Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065097 | c.1095C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065100 | c.1092C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 1.0 |
| Rv2752c | 3065115 | c.1077C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065223 | c.969T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065229 | c.963G>T | synonymous_variant | 1.0 |
| Rv2752c | 3065232 | c.960T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065241 | c.951A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065249 | c.943T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065268 | c.924A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065288 | c.904T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065292 | c.900T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065295 | p.Gln299Arg | missense_variant | 1.0 |
| Rv2752c | 3065298 | p.Asp298Glu | missense_variant | 1.0 |
| Rv2752c | 3065306 | p.Ala296Pro | missense_variant | 1.0 |
| Rv2752c | 3065311 | p.Thr294Met | missense_variant | 1.0 |
| Rv2752c | 3065313 | c.879A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065323 | p.Ala290Gly | missense_variant | 1.0 |
| Rv2752c | 3065532 | c.660A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065541 | c.651A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065553 | c.639A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065562 | c.630T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065568 | p.Ile208Val | missense_variant | 1.0 |
| Rv2752c | 3065580 | c.612G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065583 | c.609G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065589 | c.603C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 1.0 |
| Rv2752c | 3065601 | c.591C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065607 | c.585C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 1.0 |
| Rv2752c | 3065622 | c.570G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065625 | c.567G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065637 | c.555A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065640 | c.552T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065649 | c.543T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065658 | p.Pro178Leu | missense_variant | 1.0 |
| Rv2752c | 3065661 | c.531A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065666 | c.526T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065667 | c.525A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065670 | c.522C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065675 | p.Phe173Leu | missense_variant | 1.0 |
| Rv2752c | 3065699 | p.Ile165Leu | missense_variant | 1.0 |
| Rv2752c | 3065700 | c.492C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065715 | p.Tyr159His | missense_variant | 1.0 |
| Rv2752c | 3065718 | c.474G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065721 | c.471G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065727 | c.465C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065739 | c.453G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065742 | p.Thr150Ile | missense_variant | 1.0 |
| Rv2752c | 3065748 | c.444T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065768 | p.Glu142Gln | missense_variant | 1.0 |
| Rv2752c | 3065880 | c.312C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065898 | c.294C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065901 | c.291A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065916 | c.276T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065919 | c.273G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065922 | c.270T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065925 | p.Ala89Gly | missense_variant | 1.0 |
| Rv2752c | 3065928 | c.264G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065937 | c.255C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 1.0 |
| Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 1.0 |
| Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.88 |
| Rv2752c | 3065987 | p.Asp69His | missense_variant | 0.88 |
| Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.83 |
| Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.83 |
| Rv2752c | 3066000 | p.Met64Ile | missense_variant | 0.83 |
| Rv2752c | 3066009 | c.183G>C | synonymous_variant | 0.83 |
| Rv2752c | 3066027 | c.165C>G | synonymous_variant | 1.0 |
| Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 1.0 |
| Rv2752c | 3066042 | c.150T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066045 | c.147T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066050 | p.Leu48Met | missense_variant | 1.0 |
| Rv2752c | 3066054 | c.138T>G | synonymous_variant | 1.0 |
| Rv2752c | 3066066 | c.126T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>T | synonymous_variant | 0.95 |
| Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.94 |
| Rv2752c | 3066090 | p.Phe34Leu | missense_variant | 0.95 |
| Rv2752c | 3066093 | c.99T>C | synonymous_variant | 0.95 |
| Rv2752c | 3066114 | c.78A>G | synonymous_variant | 0.94 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.94 |
| Rv2752c | 3066123 | c.69C>G | synonymous_variant | 0.94 |
| Rv2752c | 3066150 | c.42C>T | synonymous_variant | 0.9 |
| Rv2752c | 3066155 | p.Ser13Ala | missense_variant | 0.67 |
| Rv2752c | 3066158 | p.Thr12Ala | missense_variant | 0.67 |
| Rv2752c | 3066252 | c.-61C>G | upstream_gene_variant | 0.95 |
| Rv2752c | 3066258 | c.-69_-67delTTGinsCTC | upstream_gene_variant | 0.95 |
| Rv2752c | 3066264 | c.-73C>G | upstream_gene_variant | 0.95 |
| Rv2752c | 3066276 | c.-87_-85delCCGinsACC | upstream_gene_variant | 0.95 |
| Rv2752c | 3066279 | c.-88A>C | upstream_gene_variant | 0.95 |
| Rv2752c | 3066285 | c.-96_-94delGCCinsCCG | upstream_gene_variant | 0.95 |
| Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 0.95 |
| Rv2752c | 3066294 | c.-103C>G | upstream_gene_variant | 0.96 |
| Rv2752c | 3066300 | c.-109G>A | upstream_gene_variant | 0.96 |
| Rv2752c | 3066320 | c.-129A>G | upstream_gene_variant | 0.95 |
| Rv2752c | 3066324 | c.-133G>A | upstream_gene_variant | 0.96 |
| Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 0.96 |
| Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 0.94 |
| Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 0.94 |
| Rv2752c | 3066345 | c.-154C>G | upstream_gene_variant | 0.94 |
| Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066366 | c.-175C>G | upstream_gene_variant | 1.0 |
| Rv2752c | 3066370 | c.-180_-179delAGinsGC | upstream_gene_variant | 1.0 |
| thyX | 3067223 | c.723G>C | synonymous_variant | 1.0 |
| thyX | 3067247 | p.Thr233Ser | missense_variant | 1.0 |
| thyX | 3067250 | p.Val232Ile | missense_variant | 1.0 |
| thyX | 3067262 | c.684C>G | synonymous_variant | 1.0 |
| thyX | 3067274 | c.672C>G | synonymous_variant | 1.0 |
| thyX | 3067277 | c.669C>A | synonymous_variant | 1.0 |
| thyX | 3067280 | p.Val222Ala | missense_variant | 1.0 |
| thyX | 3067284 | p.Ala221Gly | missense_variant | 1.0 |
| thyX | 3067288 | p.Ala220Thr | missense_variant | 1.0 |
| thyX | 3067289 | c.657C>G | synonymous_variant | 1.0 |
| thyX | 3067295 | c.651C>G | synonymous_variant | 1.0 |
| thyX | 3067304 | c.642A>G | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067319 | c.627G>C | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067328 | p.Val206Leu | missense_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 0.97 |
| thyX | 3067373 | c.573C>G | synonymous_variant | 0.91 |
| thyX | 3067376 | c.570G>C | synonymous_variant | 0.91 |
| thyX | 3067388 | c.558C>G | synonymous_variant | 0.91 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 0.91 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 0.91 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 0.95 |
| thyX | 3067463 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067470 | p.Asn159Thr | missense_variant | 1.0 |
| thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
| thyX | 3067505 | c.441G>C | synonymous_variant | 1.0 |
| thyX | 3067512 | p.Glu145Ala | missense_variant | 1.0 |
| thyX | 3067515 | p.Ser144Ala | missense_variant | 1.0 |
| thyX | 3067530 | p.Ala139Ser | missense_variant | 1.0 |
| thyX | 3067571 | c.375C>T | synonymous_variant | 1.0 |
| thyX | 3067592 | c.354G>C | synonymous_variant | 1.0 |
| thyX | 3067595 | c.351C>T | synonymous_variant | 1.0 |
| thyX | 3067598 | c.348C>T | synonymous_variant | 1.0 |
| thyX | 3067601 | c.345G>C | synonymous_variant | 1.0 |
| thyX | 3067610 | p.Lys112Asn | missense_variant | 1.0 |
| thyX | 3067616 | c.330C>G | synonymous_variant | 1.0 |
| thyX | 3067619 | c.327A>G | synonymous_variant | 1.0 |
| thyX | 3067631 | c.315C>G | synonymous_variant | 1.0 |
| thyX | 3067640 | c.306G>C | synonymous_variant | 1.0 |
| thyX | 3067652 | c.294T>C | synonymous_variant | 1.0 |
| thyX | 3067655 | c.291G>C | synonymous_variant | 1.0 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 1.0 |
| thyX | 3067667 | c.279G>C | synonymous_variant | 1.0 |
| thyX | 3067676 | c.270C>G | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>G | synonymous_variant | 1.0 |
| thyX | 3067841 | c.105G>C | synonymous_variant | 0.8 |
| thyX | 3067847 | c.99C>G | synonymous_variant | 0.91 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 0.91 |
| thyX | 3067869 | p.Thr26Asp | missense_variant | 0.89 |
| thyX | 3067874 | c.72C>G | synonymous_variant | 0.89 |
| thyX | 3067883 | c.63C>G | synonymous_variant | 0.89 |
| thyX | 3067886 | c.60A>G | synonymous_variant | 0.89 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 0.89 |
| thyX | 3067894 | p.Leu18Val | missense_variant | 0.89 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 0.89 |
| thyX | 3067904 | c.42G>A | synonymous_variant | 0.89 |
| thyX | 3067916 | c.30A>G | synonymous_variant | 0.94 |
| thyX | 3067922 | c.24C>G | synonymous_variant | 0.94 |
| thyX | 3067947 | c.-3delG | upstream_gene_variant | 0.8 |
| thyX | 3067956 | c.-11A>G | upstream_gene_variant | 0.75 |
| thyA | 3073803 | c.669G>A | synonymous_variant | 0.67 |
| thyA | 3073810 | p.Ser221Thr | missense_variant | 0.67 |
| thyA | 3073820 | c.652C>T | synonymous_variant | 0.89 |
| thyA | 3073824 | c.648A>G | synonymous_variant | 0.89 |
| thyA | 3073827 | c.645A>G | synonymous_variant | 0.9 |
| thyA | 3073839 | c.633T>C | synonymous_variant | 0.95 |
| thyA | 3073860 | c.612C>T | synonymous_variant | 0.97 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 0.94 |
| thyA | 3073872 | p.Ile200Val | missense_variant | 0.94 |
| thyA | 3073878 | c.594G>A | synonymous_variant | 0.94 |
| thyA | 3073887 | p.Ser195Ala | missense_variant | 0.94 |
| thyA | 3073896 | p.Ala192Ser | missense_variant | 0.96 |
| thyA | 3073899 | c.573G>A | synonymous_variant | 0.96 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 0.98 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 0.98 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 0.97 |
| thyA | 3073956 | c.516G>T | synonymous_variant | 0.97 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 0.97 |
| thyA | 3073962 | c.510G>C | synonymous_variant | 0.97 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073997 | c.475C>T | synonymous_variant | 1.0 |
| thyA | 3074001 | c.471C>G | synonymous_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074034 | c.438T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074056 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| thyA | 3074082 | c.390G>C | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>A | synonymous_variant | 1.0 |
| thyA | 3074100 | c.372T>C | synonymous_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| thyA | 3074121 | p.Asp117Glu | missense_variant | 1.0 |
| thyA | 3074124 | c.348G>C | synonymous_variant | 1.0 |
| thyA | 3074127 | c.345G>A | synonymous_variant | 1.0 |
| thyA | 3074147 | p.Ile109Val | missense_variant | 1.0 |
| thyA | 3074154 | c.318T>C | synonymous_variant | 1.0 |
| thyA | 3074297 | c.175C>T | synonymous_variant | 1.0 |
| thyA | 3074305 | p.Ala56Val | missense_variant | 1.0 |
| thyA | 3074307 | c.165A>G | synonymous_variant | 1.0 |
| thyA | 3074318 | p.Phe52Leu | missense_variant | 1.0 |
| thyA | 3074319 | c.153T>C | synonymous_variant | 1.0 |
| thyA | 3074322 | c.150C>G | synonymous_variant | 1.0 |
| thyA | 3074325 | c.147A>G | synonymous_variant | 1.0 |
| thyA | 3074328 | c.144G>A | synonymous_variant | 1.0 |
| thyA | 3074334 | c.138T>C | synonymous_variant | 1.0 |
| thyA | 3074349 | c.123T>C | synonymous_variant | 1.0 |
| thyA | 3074360 | c.112T>C | synonymous_variant | 1.0 |
| thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
| thyA | 3074364 | c.108T>C | synonymous_variant | 1.0 |
| thyA | 3074372 | p.Met34Leu | missense_variant | 1.0 |
| thyA | 3074373 | c.99G>A | synonymous_variant | 1.0 |
| thyA | 3074397 | c.75A>C | synonymous_variant | 0.98 |
| thyA | 3074423 | p.Pro17Ala | missense_variant | 0.98 |
| thyA | 3074427 | c.45T>C | synonymous_variant | 0.97 |
| thyA | 3074431 | p.Thr14Arg | missense_variant | 0.97 |
| thyA | 3074442 | p.Phe10Leu | missense_variant | 0.97 |
| thyA | 3074463 | c.9A>C | synonymous_variant | 0.97 |
| thyA | 3074469 | p.Val1Pro | missense_variant | 0.89 |
| thyA | 3074472 | c.-1C>T | upstream_gene_variant | 0.89 |
| thyA | 3074475 | c.-4A>G | upstream_gene_variant | 0.89 |
| thyA | 3074477 | c.-6T>C | upstream_gene_variant | 0.89 |
| thyA | 3074490 | c.-19G>A | upstream_gene_variant | 1.0 |
| ald | 3087251 | c.432T>G | synonymous_variant | 1.0 |
| ald | 3087257 | c.438T>C | synonymous_variant | 1.0 |
| ald | 3087272 | c.453A>C | synonymous_variant | 1.0 |
| ald | 3087278 | p.Gln153His | missense_variant | 1.0 |
| ald | 3087281 | c.462G>C | synonymous_variant | 1.0 |
| ald | 3087284 | c.465C>G | synonymous_variant | 1.0 |
| ald | 3087290 | c.471T>C | synonymous_variant | 1.0 |
| ald | 3087293 | c.474G>C | synonymous_variant | 1.0 |
| ald | 3087305 | c.486G>C | synonymous_variant | 1.0 |
| ald | 3087308 | c.489G>C | synonymous_variant | 1.0 |
| ald | 3087311 | c.492C>G | synonymous_variant | 1.0 |
| ald | 3087318 | p.Glu167Lys | missense_variant | 1.0 |
| ald | 3087323 | c.504G>C | synonymous_variant | 1.0 |
| ald | 3087344 | c.525C>G | synonymous_variant | 1.0 |
| ald | 3087347 | c.528C>G | synonymous_variant | 1.0 |
| ald | 3087350 | c.531C>G | synonymous_variant | 0.9 |
| ald | 3087356 | c.537C>G | synonymous_variant | 1.0 |
| ald | 3087617 | c.798T>C | synonymous_variant | 1.0 |
| ald | 3087620 | c.801A>C | synonymous_variant | 1.0 |
| ald | 3087621 | p.Ala268Ser | missense_variant | 1.0 |
| ald | 3087641 | c.822T>C | synonymous_variant | 1.0 |
| ald | 3087647 | c.828A>G | synonymous_variant | 1.0 |
| ald | 3087649 | p.Gly277Asp | missense_variant | 1.0 |
| ald | 3087653 | c.834A>G | synonymous_variant | 1.0 |
| ald | 3087656 | c.837A>C | synonymous_variant | 1.0 |
| ald | 3087666 | p.Tyr283His | missense_variant | 1.0 |
| ald | 3087672 | p.His285Asp | missense_variant | 1.0 |
| ald | 3087704 | c.885T>C | synonymous_variant | 1.0 |
| ald | 3087716 | c.897G>C | synonymous_variant | 1.0 |
| ald | 3087726 | p.Ala303Ser | missense_variant | 1.0 |
| ald | 3087729 | p.Ser304Ala | missense_variant | 1.0 |
| ald | 3087734 | c.915G>T | synonymous_variant | 1.0 |
| ald | 3087743 | c.924G>C | synonymous_variant | 1.0 |
| ald | 3087750 | p.Tyr311Val | missense_variant | 1.0 |
| ald | 3087767 | c.948G>C | synonymous_variant | 1.0 |
| ald | 3087770 | c.951G>C | synonymous_variant | 1.0 |
| fbiD | 3339606 | c.489G>C | synonymous_variant | 0.6 |
| fbiD | 3339607 | p.Pro164Ala | missense_variant | 0.6 |
| fbiD | 3339616 | p.Ser167Ala | missense_variant | 0.71 |
| fbiD | 3339621 | c.504G>A | synonymous_variant | 0.71 |
| fbiD | 3339642 | c.525T>C | synonymous_variant | 0.71 |
| fbiD | 3339643 | p.Val176Ile | missense_variant | 0.71 |
| fbiD | 3339654 | c.537A>C | synonymous_variant | 1.0 |
| fbiD | 3339657 | c.540A>C | synonymous_variant | 1.0 |
| fbiD | 3339666 | c.549G>C | synonymous_variant | 1.0 |
| fbiD | 3339669 | c.552C>G | synonymous_variant | 1.0 |
| fbiD | 3339681 | c.564T>C | synonymous_variant | 1.0 |
| fbiD | 3339690 | c.573C>G | synonymous_variant | 1.0 |
| fbiD | 3339691 | p.Pro192Ser | missense_variant | 1.0 |
| fbiD | 3339703 | p.Thr196Ala | missense_variant | 1.0 |
| fprA | 3473812 | c.-195G>A | upstream_gene_variant | 1.0 |
| fprA | 3473842 | c.-165_-164delGCinsCG | upstream_gene_variant | 1.0 |
| fprA | 3473848 | c.-159_-157delCAAinsAAG | upstream_gene_variant | 1.0 |
| fprA | 3473869 | c.-138A>C | upstream_gene_variant | 1.0 |
| fprA | 3473878 | c.-129G>T | upstream_gene_variant | 1.0 |
| fprA | 3473886 | c.-121C>G | upstream_gene_variant | 1.0 |
| fprA | 3474106 | p.Met34Val | missense_variant | 1.0 |
| fprA | 3474109 | p.Ala35Thr | missense_variant | 1.0 |
| fprA | 3474121 | c.115C>T | synonymous_variant | 1.0 |
| fprA | 3474130 | c.124T>C | synonymous_variant | 1.0 |
| fprA | 3474138 | c.132T>A | synonymous_variant | 1.0 |
| fprA | 3474141 | c.135C>G | synonymous_variant | 1.0 |
| fprA | 3474147 | c.141G>C | synonymous_variant | 1.0 |
| fprA | 3474159 | c.153C>G | synonymous_variant | 1.0 |
| fprA | 3474162 | c.156G>C | synonymous_variant | 1.0 |
| fprA | 3474174 | c.168T>C | synonymous_variant | 1.0 |
| fprA | 3474210 | c.204A>G | synonymous_variant | 1.0 |
| fprA | 3474219 | c.213C>G | synonymous_variant | 1.0 |
| fprA | 3474220 | p.Glu72Gln | missense_variant | 1.0 |
| fprA | 3474228 | c.222C>G | synonymous_variant | 1.0 |
| fprA | 3474231 | c.225C>G | synonymous_variant | 1.0 |
| fprA | 3474249 | c.243T>C | synonymous_variant | 1.0 |
| fprA | 3474261 | c.255C>G | synonymous_variant | 1.0 |
| fprA | 3474264 | c.258A>G | synonymous_variant | 1.0 |
| fprA | 3474270 | c.264C>G | synonymous_variant | 1.0 |
| fprA | 3474273 | p.Gln89His | missense_variant | 1.0 |
| fprA | 3474274 | p.Pro90Ala | missense_variant | 1.0 |
| fprA | 3474277 | p.Gly91His | missense_variant | 1.0 |
| fprA | 3474286 | p.Ser94Ala | missense_variant | 1.0 |
| fprA | 3474306 | c.300G>C | synonymous_variant | 1.0 |
| fprA | 3474318 | c.312C>G | synonymous_variant | 1.0 |
| fprA | 3474333 | c.327T>C | synonymous_variant | 1.0 |
| fprA | 3474337 | p.Met111Ala | missense_variant | 1.0 |
| fprA | 3474340 | c.334_336delTTGinsCTC | synonymous_variant | 1.0 |
| fprA | 3474343 | p.Asn113Gly | missense_variant | 1.0 |
| fprA | 3474354 | c.348T>C | synonymous_variant | 1.0 |
| fprA | 3474366 | c.360G>C | synonymous_variant | 1.0 |
| fprA | 3474372 | c.366T>C | synonymous_variant | 1.0 |
| fprA | 3474387 | c.381T>C | synonymous_variant | 1.0 |
| fprA | 3475061 | p.Pro352Arg | missense_variant | 0.67 |
| fprA | 3475068 | c.1062A>G | synonymous_variant | 0.67 |
| fprA | 3475080 | c.1074G>C | synonymous_variant | 0.67 |
| fprA | 3475095 | c.1089G>C | synonymous_variant | 0.67 |
| fprA | 3475104 | c.1098G>T | synonymous_variant | 0.67 |
| fprA | 3475107 | c.1101G>C | synonymous_variant | 0.67 |
| fprA | 3475113 | c.1107G>C | synonymous_variant | 0.67 |
| fprA | 3475119 | c.1113C>T | synonymous_variant | 0.67 |
| fprA | 3475129 | p.Ala375Ser | missense_variant | 1.0 |
| Rv3236c | 3612621 | c.496T>C | synonymous_variant | 1.0 |
| Rv3236c | 3612643 | c.474A>G | synonymous_variant | 1.0 |
| Rv3236c | 3612649 | c.468G>A | synonymous_variant | 1.0 |
| Rv3236c | 3612652 | c.465G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612664 | c.453G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612667 | p.Ala150Ser | missense_variant | 1.0 |
| Rv3236c | 3612676 | c.441A>G | synonymous_variant | 1.0 |
| Rv3236c | 3612679 | p.Arg146Leu | missense_variant | 1.0 |
| Rv3236c | 3612688 | c.429C>G | synonymous_variant | 1.0 |
| Rv3236c | 3612694 | c.423T>C | synonymous_variant | 1.0 |
| fbiA | 3640708 | p.Leu56Val | missense_variant | 1.0 |
| fbiB | 3640713 | c.-822T>G | upstream_gene_variant | 1.0 |
| fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640747 | c.-788C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640797 | c.-738T>C | upstream_gene_variant | 0.67 |
| fbiA | 3640808 | p.Met89Lys | missense_variant | 0.75 |
| fbiA | 3640810 | p.Gln90Glu | missense_variant | 0.75 |
| fbiB | 3640816 | c.-719C>T | upstream_gene_variant | 0.75 |
| fbiA | 3640820 | p.Val93Ala | missense_variant | 0.75 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 0.75 |
| fbiB | 3640830 | c.-705C>G | upstream_gene_variant | 0.78 |
| fbiA | 3640850 | p.Glu103Gly | missense_variant | 0.8 |
| fbiB | 3640854 | c.-681C>G | upstream_gene_variant | 0.75 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 0.86 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 0.83 |
| fbiA | 3640871 | p.Ala110Gly | missense_variant | 0.8 |
| fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640899 | c.-636G>C | upstream_gene_variant | 1.0 |
| fbiA | 3641260 | p.Ile240Val | missense_variant | 1.0 |
| fbiA | 3641281 | p.Ile247Val | missense_variant | 1.0 |
| fbiA | 3641285 | p.Gly248Ala | missense_variant | 1.0 |
| fbiA | 3641288 | p.Glu249Gly | missense_variant | 0.75 |
| fbiB | 3641292 | c.-243G>A | upstream_gene_variant | 1.0 |
| fbiA | 3641314 | p.Thr258Ala | missense_variant | 1.0 |
| fbiB | 3641328 | c.-207T>G | upstream_gene_variant | 1.0 |
| fbiB | 3641334 | c.-201G>C | upstream_gene_variant | 1.0 |
| fbiA | 3641340 | p.Asp266Glu | missense_variant | 1.0 |
| fbiB | 3641355 | c.-180T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641358 | c.-177G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641379 | c.-156G>C | upstream_gene_variant | 0.94 |
| fbiA | 3641380 | p.Cys280Arg | missense_variant | 0.94 |
| fbiA | 3641384 | p.Ala281Gly | missense_variant | 0.94 |
| fbiB | 3641394 | c.-141A>C | upstream_gene_variant | 0.94 |
| fbiB | 3641412 | c.-123G>C | upstream_gene_variant | 0.67 |
| fbiA | 3641413 | p.His291Asp | missense_variant | 0.67 |
| fbiA | 3641417 | p.Asp292Ala | missense_variant | 0.67 |
| fbiA | 3641425 | p.His295Gly | missense_variant | 0.5 |
| fbiB | 3641430 | c.-105T>C | upstream_gene_variant | 0.5 |
| fbiA | 3641433 | p.Glu297Asp | missense_variant | 0.5 |
| fbiB | 3641436 | c.-99T>C | upstream_gene_variant | 0.5 |
| fbiA | 3641446 | p.Thr302Ala | missense_variant | 0.5 |
| fbiB | 3641454 | c.-81G>C | upstream_gene_variant | 0.5 |
| fbiA | 3641455 | p.Ser305Ala | missense_variant | 0.5 |
| fbiB | 3641467 | c.-68C>T | upstream_gene_variant | 0.67 |
| fbiB | 3641891 | c.357G>C | synonymous_variant | 0.67 |
| fbiB | 3641906 | c.372T>C | synonymous_variant | 0.83 |
| fbiB | 3641909 | c.375T>C | synonymous_variant | 0.83 |
| fbiB | 3641918 | c.384T>C | synonymous_variant | 0.83 |
| fbiB | 3641957 | c.423C>G | synonymous_variant | 1.0 |
| fbiB | 3641960 | c.426C>G | synonymous_variant | 1.0 |
| fbiB | 3641961 | p.Thr143Arg | missense_variant | 1.0 |
| fbiB | 3641972 | c.438G>C | synonymous_variant | 1.0 |
| fbiB | 3641981 | c.447C>G | synonymous_variant | 1.0 |
| fbiB | 3641987 | c.453C>G | synonymous_variant | 1.0 |
| fbiB | 3641993 | c.459A>C | synonymous_variant | 1.0 |
| fbiB | 3642560 | c.1026T>C | synonymous_variant | 1.0 |
| fbiB | 3642566 | c.1032A>G | synonymous_variant | 1.0 |
| fbiB | 3642572 | c.1038A>G | synonymous_variant | 1.0 |
| fbiB | 3642581 | c.1047A>C | synonymous_variant | 1.0 |
| fbiB | 3642602 | c.1068A>C | synonymous_variant | 1.0 |
| fbiB | 3642605 | c.1071A>C | synonymous_variant | 1.0 |
| fbiB | 3642609 | p.Ser359Asp | missense_variant | 1.0 |
| fbiB | 3642614 | c.1080C>T | synonymous_variant | 1.0 |
| fbiB | 3642620 | c.1086T>C | synonymous_variant | 1.0 |
| fbiB | 3642626 | c.1092C>G | synonymous_variant | 1.0 |
| fbiB | 3642634 | p.Asp367Ala | missense_variant | 1.0 |
| fbiB | 3642656 | c.1122G>C | synonymous_variant | 1.0 |
| fbiB | 3642662 | c.1128C>G | synonymous_variant | 1.0 |
| fbiB | 3642665 | c.1131C>G | synonymous_variant | 1.0 |
| fbiB | 3642668 | c.1134A>C | synonymous_variant | 1.0 |
| fbiB | 3642677 | c.1143A>G | synonymous_variant | 1.0 |
| fbiB | 3642680 | c.1146A>G | synonymous_variant | 1.0 |
| fbiB | 3642684 | c.1150T>C | synonymous_variant | 1.0 |
| fbiB | 3642692 | c.1158C>G | synonymous_variant | 1.0 |
| fbiB | 3642707 | c.1173C>G | synonymous_variant | 1.0 |
| fbiB | 3642711 | p.Leu393Val | missense_variant | 1.0 |
| fbiB | 3642719 | c.1185T>C | synonymous_variant | 1.0 |
| alr | 3840248 | c.1173C>G | synonymous_variant | 1.0 |
| alr | 3840254 | c.1167A>G | synonymous_variant | 1.0 |
| alr | 3840274 | p.Val383Leu | missense_variant | 1.0 |
| alr | 3840275 | c.1146T>G | synonymous_variant | 1.0 |
| alr | 3840278 | c.1143T>C | synonymous_variant | 1.0 |
| alr | 3840281 | c.1140C>G | synonymous_variant | 1.0 |
| alr | 3840293 | c.1128T>G | synonymous_variant | 1.0 |
| alr | 3840371 | c.1050G>A | synonymous_variant | 1.0 |
| alr | 3840380 | p.Met347Val | missense_variant | 0.67 |
| alr | 3840404 | c.1017G>C | synonymous_variant | 0.67 |
| alr | 3840407 | c.1014G>C | synonymous_variant | 0.67 |
| alr | 3840410 | c.1011T>C | synonymous_variant | 0.67 |
| alr | 3840416 | p.Cys335Arg | missense_variant | 0.67 |
| alr | 3840419 | c.1002A>C | synonymous_variant | 0.67 |
| alr | 3840422 | c.997_999delAGAinsCGG | synonymous_variant | 0.67 |
| alr | 3840442 | p.Glu327Gln | missense_variant | 0.5 |
| rpoA | 3877494 | p.Glu338Asp | missense_variant | 1.0 |
| rpoA | 3877503 | c.1005G>C | synonymous_variant | 1.0 |
| rpoA | 3877506 | c.1002C>A | synonymous_variant | 1.0 |
| rpoA | 3877530 | c.978C>G | synonymous_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.97 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 0.97 |
| rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.97 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 0.94 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 0.93 |
| rpoA | 3877617 | c.891G>C | synonymous_variant | 0.92 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 0.97 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 0.96 |
| rpoA | 3877677 | p.Ala277Ser | missense_variant | 0.98 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877746 | c.762G>C | synonymous_variant | 1.0 |
| rpoA | 3877763 | c.745C>T | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877841 | c.667C>A | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877872 | c.636C>T | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877884 | c.624G>C | synonymous_variant | 1.0 |
| rpoA | 3877900 | p.Ser203Thr | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>C | synonymous_variant | 1.0 |
| rpoA | 3877908 | p.Asn200Ser | missense_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877923 | c.585C>T | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877929 | p.Ile193Val | missense_variant | 1.0 |
| rpoA | 3877962 | c.546G>C | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878013 | c.495T>C | synonymous_variant | 1.0 |
| rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878034 | c.474A>G | synonymous_variant | 1.0 |
| rpoA | 3878043 | c.465G>C | synonymous_variant | 1.0 |
| rpoA | 3878046 | c.462T>G | synonymous_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 0.6 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 0.67 |
| rpoA | 3878124 | c.384G>C | synonymous_variant | 0.67 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 0.67 |
| rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.71 |
| rpoA | 3878157 | c.351C>G | synonymous_variant | 0.92 |
| rpoA | 3878166 | c.342C>G | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>C | synonymous_variant | 1.0 |
| rpoA | 3878184 | c.324C>T | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878197 | p.Glu104Ala | missense_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878253 | c.255G>T | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878284 | p.Glu75Ala | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878304 | c.204G>C | synonymous_variant | 1.0 |
| rpoA | 3878307 | p.Pro67Gln | missense_variant | 1.0 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
| rpoA | 3878334 | c.174T>G | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 1.0 |
| rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 1.0 |
| ddn | 3986657 | c.-187C>G | upstream_gene_variant | 1.0 |
| ddn | 3986665 | c.-179_-178delGCinsCG | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 1.0 |
| ddn | 3986673 | c.-171C>T | upstream_gene_variant | 1.0 |
| ddn | 3986696 | c.-148G>C | upstream_gene_variant | 1.0 |
| ddn | 3986699 | c.-145C>G | upstream_gene_variant | 1.0 |
| ddn | 3986714 | c.-130C>G | upstream_gene_variant | 1.0 |
| ddn | 3986726 | c.-118G>C | upstream_gene_variant | 1.0 |
| clpC1 | 4038200 | c.2505T>C | synonymous_variant | 1.0 |
| clpC1 | 4038206 | c.2499C>G | synonymous_variant | 1.0 |
| clpC1 | 4038212 | c.2493T>C | synonymous_variant | 1.0 |
| clpC1 | 4038215 | c.2490G>C | synonymous_variant | 1.0 |
| clpC1 | 4038218 | c.2487G>A | synonymous_variant | 1.0 |
| clpC1 | 4038238 | p.Thr823Ala | missense_variant | 1.0 |
| clpC1 | 4038239 | c.2466T>C | synonymous_variant | 1.0 |
| clpC1 | 4038270 | p.Pro812Ser | missense_variant | 1.0 |
| clpC1 | 4038272 | c.2433T>C | synonymous_variant | 1.0 |
| clpC1 | 4038275 | c.2430A>G | synonymous_variant | 1.0 |
| clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
| clpC1 | 4038308 | c.2397G>C | synonymous_variant | 1.0 |
| clpC1 | 4038317 | c.2388G>C | synonymous_variant | 1.0 |
| clpC1 | 4038320 | c.2385G>T | synonymous_variant | 1.0 |
| clpC1 | 4038323 | p.Val794Leu | missense_variant | 1.0 |
| clpC1 | 4038350 | c.2355C>G | synonymous_variant | 1.0 |
| clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
| clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
| clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
| clpC1 | 4038374 | c.2331C>T | synonymous_variant | 1.0 |
| clpC1 | 4038395 | c.2310C>G | synonymous_variant | 1.0 |
| clpC1 | 4038398 | c.2307G>C | synonymous_variant | 1.0 |
| clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
| clpC1 | 4038410 | c.2295C>T | synonymous_variant | 1.0 |
| clpC1 | 4038416 | c.2289C>T | synonymous_variant | 1.0 |
| clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
| clpC1 | 4038433 | c.2272C>T | synonymous_variant | 1.0 |
| clpC1 | 4038436 | p.Ala757Ser | missense_variant | 1.0 |
| clpC1 | 4038440 | c.2265C>G | synonymous_variant | 1.0 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
| clpC1 | 4038446 | p.Asp753Glu | missense_variant | 1.0 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
| clpC1 | 4038460 | c.2245C>T | synonymous_variant | 1.0 |
| clpC1 | 4038474 | p.Ser744Ala | missense_variant | 1.0 |
| clpC1 | 4038486 | p.Gly740Asn | missense_variant | 1.0 |
| clpC1 | 4038489 | p.Ala739Gly | missense_variant | 1.0 |
| clpC1 | 4038502 | p.Ile735Val | missense_variant | 1.0 |
| clpC1 | 4038506 | c.2199G>C | synonymous_variant | 1.0 |
| clpC1 | 4038519 | p.Arg729Lys | missense_variant | 1.0 |
| clpC1 | 4038537 | p.Thr723Ser | missense_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038640 | p.Asp689Asn | missense_variant | 1.0 |
| clpC1 | 4038658 | p.Lys683Gln | missense_variant | 1.0 |
| clpC1 | 4038661 | p.Ser682Thr | missense_variant | 1.0 |
| clpC1 | 4038662 | c.2043T>C | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038693 | p.Ser671Gly | missense_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038721 | c.1984C>T | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038884 | c.1821C>T | synonymous_variant | 1.0 |
| clpC1 | 4038899 | c.1806C>G | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039090 | c.1615C>T | synonymous_variant | 1.0 |
| clpC1 | 4039094 | c.1611C>G | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039118 | c.1587C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039187 | c.1518G>C | synonymous_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 1.0 |
| clpC1 | 4039295 | c.1410A>C | synonymous_variant | 1.0 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 1.0 |
| clpC1 | 4039310 | c.1395A>G | synonymous_variant | 1.0 |
| clpC1 | 4039319 | p.Ala462Ser | missense_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>G | synonymous_variant | 1.0 |
| clpC1 | 4039331 | c.1374C>G | synonymous_variant | 1.0 |
| clpC1 | 4039338 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039346 | c.1359G>C | synonymous_variant | 1.0 |
| clpC1 | 4039359 | p.Ser449Asn | missense_variant | 1.0 |
| clpC1 | 4039361 | c.1344C>G | synonymous_variant | 1.0 |
| clpC1 | 4039364 | c.1341C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>G | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039553 | c.1152C>G | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>C | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039571 | c.1134G>C | synonymous_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
| clpC1 | 4039655 | c.1050G>C | synonymous_variant | 0.81 |
| clpC1 | 4039658 | c.1047G>A | synonymous_variant | 0.81 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.84 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
| clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>G | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039871 | c.834C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>T | synonymous_variant | 1.0 |
| clpC1 | 4039996 | p.Glu237Gln | missense_variant | 1.0 |
| clpC1 | 4039997 | c.708C>G | synonymous_variant | 0.95 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040027 | c.678C>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040138 | c.567G>C | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040168 | c.537G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040200 | c.505T>C | synonymous_variant | 1.0 |
| clpC1 | 4040201 | c.504C>G | synonymous_variant | 1.0 |
| clpC1 | 4040207 | c.498T>C | synonymous_variant | 1.0 |
| clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040225 | c.480A>C | synonymous_variant | 1.0 |
| clpC1 | 4040228 | c.477G>C | synonymous_variant | 1.0 |
| clpC1 | 4040231 | c.474C>T | synonymous_variant | 1.0 |
| clpC1 | 4040237 | c.468C>T | synonymous_variant | 1.0 |
| clpC1 | 4040240 | c.465C>G | synonymous_variant | 1.0 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040252 | c.453C>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040324 | c.381G>C | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040366 | c.339C>T | synonymous_variant | 1.0 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040414 | c.291G>A | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>G | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040528 | c.177G>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
| clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040567 | c.138C>G | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040585 | c.120A>G | synonymous_variant | 1.0 |
| clpC1 | 4040588 | c.117T>C | synonymous_variant | 1.0 |
| clpC1 | 4040596 | c.109C>T | synonymous_variant | 0.67 |
| clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.67 |
| clpC1 | 4040600 | c.105A>G | synonymous_variant | 0.67 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.67 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.75 |
| clpC1 | 4040618 | c.87C>G | synonymous_variant | 0.85 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.92 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| clpC1 | 4040695 | c.10C>A | synonymous_variant | 1.0 |
| clpC1 | 4040699 | c.6C>T | synonymous_variant | 1.0 |
| clpC1 | 4040706 | c.-4_-3delAC | upstream_gene_variant | 1.0 |
| clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040730 | c.-26T>A | upstream_gene_variant | 1.0 |
| panD | 4044093 | c.189A>G | synonymous_variant | 1.0 |
| panD | 4044105 | c.177G>C | synonymous_variant | 1.0 |
| panD | 4044108 | c.174C>T | synonymous_variant | 1.0 |
| panD | 4044126 | c.156T>C | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044150 | c.132A>G | synonymous_variant | 1.0 |
| panD | 4044162 | c.120A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>C | synonymous_variant | 1.0 |
| panD | 4044171 | c.111C>T | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044204 | c.78G>C | synonymous_variant | 1.0 |
| panD | 4044237 | c.45G>C | synonymous_variant | 1.0 |
| panD | 4044240 | c.42G>C | synonymous_variant | 1.0 |
| panD | 4044264 | c.18G>C | synonymous_variant | 1.0 |
| panD | 4044287 | c.-6A>G | upstream_gene_variant | 1.0 |
| panD | 4044294 | c.-13A>C | upstream_gene_variant | 1.0 |
| panD | 4044299 | c.-18A>G | upstream_gene_variant | 1.0 |
| embC | 4239668 | c.-195G>C | upstream_gene_variant | 1.0 |
| embC | 4239671 | c.-192C>G | upstream_gene_variant | 1.0 |
| embC | 4239674 | c.-189C>G | upstream_gene_variant | 1.0 |
| embC | 4239680 | c.-183C>G | upstream_gene_variant | 1.0 |
| embC | 4239688 | c.-175A>G | upstream_gene_variant | 1.0 |
| embC | 4239695 | c.-168A>C | upstream_gene_variant | 1.0 |
| embC | 4239696 | c.-167_-165delCATinsGAC | upstream_gene_variant | 1.0 |
| embC | 4239703 | c.-160G>A | upstream_gene_variant | 1.0 |
| embC | 4239723 | c.-140C>G | upstream_gene_variant | 1.0 |
| embC | 4239749 | c.-114T>C | upstream_gene_variant | 1.0 |
| embC | 4240019 | p.Asn53Asp | missense_variant | 0.75 |
| embC | 4240033 | c.171G>C | synonymous_variant | 0.75 |
| embC | 4240036 | c.174A>G | synonymous_variant | 0.75 |
| embC | 4240037 | c.175_177delTTGinsCTC | synonymous_variant | 0.75 |
| embC | 4240048 | c.186C>G | synonymous_variant | 1.0 |
| embC | 4240051 | c.189A>G | synonymous_variant | 1.0 |
| embC | 4240053 | p.Asn64Ser | missense_variant | 1.0 |
| embC | 4240064 | p.Ala68Thr | missense_variant | 0.93 |
| embC | 4240069 | c.207T>C | synonymous_variant | 0.93 |
| embC | 4240078 | c.216A>G | synonymous_variant | 0.93 |
| embC | 4240084 | c.222G>C | synonymous_variant | 0.94 |
| embC | 4240087 | c.225T>C | synonymous_variant | 0.94 |
| embC | 4240105 | p.Asp81Glu | missense_variant | 0.93 |
| embC | 4240106 | p.Leu82Met | missense_variant | 0.93 |
| embC | 4240110 | p.Asn83Thr | missense_variant | 0.93 |
| embC | 4240112 | p.Ile84Val | missense_variant | 0.93 |
| embC | 4240120 | c.258C>G | synonymous_variant | 0.96 |
| embC | 4240150 | c.288A>G | synonymous_variant | 0.92 |
| embC | 4240151 | p.Ser97Pro | missense_variant | 0.92 |
| embC | 4240160 | p.Thr100Ala | missense_variant | 0.92 |
| embC | 4240171 | c.309G>C | synonymous_variant | 1.0 |
| embC | 4240175 | c.313T>C | synonymous_variant | 1.0 |
| embC | 4240183 | c.321A>G | synonymous_variant | 1.0 |
| embC | 4240201 | c.339G>C | synonymous_variant | 1.0 |
| embC | 4240204 | c.342T>G | synonymous_variant | 1.0 |
| embC | 4240216 | c.354T>C | synonymous_variant | 1.0 |
| embC | 4240420 | c.558T>C | synonymous_variant | 1.0 |
| embC | 4240424 | p.Arg188Lys | missense_variant | 1.0 |
| embC | 4240432 | c.570C>T | synonymous_variant | 1.0 |
| embC | 4240444 | c.582C>G | synonymous_variant | 1.0 |
| embC | 4240459 | c.597G>C | synonymous_variant | 1.0 |
| embC | 4240462 | c.600G>C | synonymous_variant | 1.0 |
| embC | 4240483 | c.621G>C | synonymous_variant | 1.0 |
| embC | 4240489 | c.627A>G | synonymous_variant | 1.0 |
| embC | 4240491 | p.Pro210Gln | missense_variant | 1.0 |
| embC | 4240495 | c.633T>G | synonymous_variant | 1.0 |
| embC | 4240500 | p.Ser213Asn | missense_variant | 1.0 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 1.0 |
| embC | 4240514 | p.Val218Ile | missense_variant | 1.0 |
| embC | 4240519 | c.657T>C | synonymous_variant | 1.0 |
| embC | 4240535 | p.Ser225His | missense_variant | 1.0 |
| embC | 4240543 | c.681G>C | synonymous_variant | 1.0 |
| embC | 4240642 | c.780G>C | synonymous_variant | 0.88 |
| embC | 4240645 | c.783G>C | synonymous_variant | 0.8 |
| embC | 4240654 | c.792C>G | synonymous_variant | 0.73 |
| embC | 4240655 | p.Ala265Ser | missense_variant | 0.82 |
| embC | 4240670 | p.Thr270Val | missense_variant | 0.91 |
| embC | 4240678 | c.816T>C | synonymous_variant | 0.94 |
| embC | 4240685 | p.Thr275Ala | missense_variant | 0.94 |
| embC | 4240693 | c.831T>C | synonymous_variant | 0.95 |
| embC | 4240717 | p.His285Gln | missense_variant | 0.98 |
| embC | 4240726 | c.864G>C | synonymous_variant | 0.98 |
| embC | 4240756 | c.894G>C | synonymous_variant | 1.0 |
| embC | 4240777 | c.915G>A | synonymous_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240819 | c.957A>C | synonymous_variant | 0.96 |
| embC | 4240831 | c.969T>C | synonymous_variant | 0.97 |
| embC | 4240855 | c.993G>C | synonymous_variant | 0.96 |
| embC | 4240867 | c.1005T>G | synonymous_variant | 1.0 |
| embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |
| embC | 4240875 | p.Ser338Thr | missense_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_variant | 1.0 |
| embC | 4240880 | p.Ala340Ser | missense_variant | 0.97 |
| embC | 4240885 | c.1023T>C | synonymous_variant | 0.97 |
| embC | 4240900 | c.1038A>G | synonymous_variant | 0.97 |
| embC | 4240912 | c.1050G>C | synonymous_variant | 0.95 |
| embC | 4240921 | c.1059C>G | synonymous_variant | 0.93 |
| embC | 4240936 | c.1074A>G | synonymous_variant | 0.67 |
| embC | 4240945 | c.1083T>C | synonymous_variant | 0.67 |
| embC | 4241017 | c.1155T>C | synonymous_variant | 0.75 |
| embC | 4241023 | c.1161T>C | synonymous_variant | 0.93 |
| embC | 4241039 | p.Asp393Asn | missense_variant | 0.95 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 0.95 |
| embC | 4241053 | c.1191G>C | synonymous_variant | 0.95 |
| embC | 4241056 | c.1194C>G | synonymous_variant | 1.0 |
| embC | 4241059 | c.1197G>A | synonymous_variant | 1.0 |
| embC | 4241071 | c.1209C>G | synonymous_variant | 0.96 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 0.96 |
| embC | 4241137 | c.1275G>C | synonymous_variant | 0.96 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 0.96 |
| embC | 4241153 | p.Ile431Leu | missense_variant | 0.97 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 0.97 |
| embC | 4241162 | c.1300_1302delTTGinsCTC | synonymous_variant | 0.97 |
| embC | 4241179 | c.1317G>T | synonymous_variant | 0.98 |
| embC | 4241194 | c.1332C>G | synonymous_variant | 0.98 |
| embC | 4241197 | c.1335G>C | synonymous_variant | 0.98 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 0.98 |
| embC | 4241224 | c.1362G>C | synonymous_variant | 0.95 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 0.94 |
| embC | 4241251 | c.1389T>G | synonymous_variant | 0.8 |
| embC | 4241256 | p.Arg465Thr | missense_variant | 0.8 |
| embC | 4241266 | c.1404C>G | synonymous_variant | 0.67 |
| embC | 4241353 | p.Ile497Met | missense_variant | 1.0 |
| embC | 4241361 | p.Asn500Thr | missense_variant | 1.0 |
| embC | 4241363 | p.Leu501Ala | missense_variant | 1.0 |
| embC | 4241374 | c.1512T>C | synonymous_variant | 1.0 |
| embC | 4241380 | c.1518A>C | synonymous_variant | 1.0 |
| embC | 4241394 | p.Lys511Ser | missense_variant | 1.0 |
| embC | 4241437 | c.1575C>G | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>T | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241458 | c.1596C>G | synonymous_variant | 1.0 |
| embC | 4241470 | c.1608C>G | synonymous_variant | 1.0 |
| embC | 4241479 | c.1617C>G | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>C | synonymous_variant | 1.0 |
| embC | 4241554 | c.1692G>C | synonymous_variant | 1.0 |
| embC | 4241560 | c.1698C>G | synonymous_variant | 1.0 |
| embC | 4241567 | p.Ile569Leu | missense_variant | 1.0 |
| embC | 4241572 | c.1710C>G | synonymous_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241591 | p.Leu577Val | missense_variant | 1.0 |
| embC | 4241611 | c.1749G>C | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embC | 4241623 | c.1761C>G | synonymous_variant | 1.0 |
| embC | 4241626 | c.1764T>C | synonymous_variant | 1.0 |
| embC | 4241644 | c.1782G>C | synonymous_variant | 1.0 |
| embC | 4241648 | c.1786T>C | synonymous_variant | 1.0 |
| embC | 4241657 | p.Ser599Pro | missense_variant | 1.0 |
| embC | 4241665 | c.1803G>C | synonymous_variant | 1.0 |
| embC | 4241671 | c.1809T>G | synonymous_variant | 1.0 |
| embC | 4241677 | c.1815G>C | synonymous_variant | 1.0 |
| embC | 4241683 | c.1821G>C | synonymous_variant | 1.0 |
| embC | 4241741 | p.Val627Leu | missense_variant | 1.0 |
| embC | 4241747 | p.Val629Leu | missense_variant | 1.0 |
| embC | 4241750 | p.Leu630Met | missense_variant | 1.0 |
| embC | 4241755 | c.1893C>G | synonymous_variant | 1.0 |
| embC | 4241756 | c.1894C>T | synonymous_variant | 1.0 |
| embC | 4241770 | c.1908T>C | synonymous_variant | 1.0 |
| embC | 4241788 | c.1926C>T | synonymous_variant | 1.0 |
| embC | 4241794 | c.1932C>G | synonymous_variant | 1.0 |
| embC | 4241797 | c.1935C>T | synonymous_variant | 1.0 |
| embC | 4241809 | c.1947A>C | synonymous_variant | 1.0 |
| embC | 4241818 | c.1956C>T | synonymous_variant | 1.0 |
| embC | 4242229 | c.2367C>A | synonymous_variant | 0.83 |
| embC | 4242245 | p.Thr795Arg | missense_variant | 0.86 |
| embA | 4242256 | c.-977G>C | upstream_gene_variant | 0.86 |
| embA | 4242268 | c.-965T>C | upstream_gene_variant | 1.0 |
| embA | 4242271 | c.-962A>G | upstream_gene_variant | 1.0 |
| embA | 4242274 | c.-959G>C | upstream_gene_variant | 1.0 |
| embA | 4242277 | c.-956T>C | upstream_gene_variant | 1.0 |
| embA | 4242283 | c.-950T>C | upstream_gene_variant | 1.0 |
| embC | 4242287 | p.Leu809Val | missense_variant | 1.0 |
| embC | 4242291 | p.Asn810Ser | missense_variant | 1.0 |
| embA | 4242301 | c.-932G>C | upstream_gene_variant | 1.0 |
| embC | 4242302 | p.Leu814Val | missense_variant | 1.0 |
| embC | 4242305 | p.Ile815Val | missense_variant | 1.0 |
| embA | 4242691 | c.-542C>G | upstream_gene_variant | 1.0 |
| embA | 4242694 | c.-539G>T | upstream_gene_variant | 1.0 |
| embA | 4242695 | c.-538T>C | upstream_gene_variant | 1.0 |
| embA | 4242700 | c.-533C>G | upstream_gene_variant | 1.0 |
| embC | 4242710 | p.Gln950Glu | missense_variant | 1.0 |
| embA | 4242715 | c.-518T>C | upstream_gene_variant | 1.0 |
| embA | 4242739 | c.-494C>G | upstream_gene_variant | 1.0 |
| embA | 4242742 | c.-491C>G | upstream_gene_variant | 1.0 |
| embA | 4242745 | c.-488A>C | upstream_gene_variant | 1.0 |
| embA | 4242748 | c.-485A>G | upstream_gene_variant | 1.0 |
| embA | 4242754 | c.-479G>C | upstream_gene_variant | 1.0 |
| embA | 4242757 | c.-476T>C | upstream_gene_variant | 1.0 |
| embC | 4242764 | p.Val968Leu | missense_variant | 1.0 |
| embA | 4242772 | c.-461G>A | upstream_gene_variant | 1.0 |
| embC | 4242779 | p.Asn973Asp | missense_variant | 1.0 |
| embC | 4242791 | p.Ala977Ser | missense_variant | 1.0 |
| embA | 4242796 | c.-437G>A | upstream_gene_variant | 1.0 |
| embA | 4242799 | c.-434T>C | upstream_gene_variant | 1.0 |
| embA | 4242823 | c.-410G>C | upstream_gene_variant | 1.0 |
| embA | 4242832 | c.-401A>G | upstream_gene_variant | 0.97 |
| embA | 4242835 | c.-398C>T | upstream_gene_variant | 0.96 |
| embA | 4242844 | c.-389A>G | upstream_gene_variant | 0.97 |
| embA | 4242847 | c.-386C>G | upstream_gene_variant | 0.93 |
| embA | 4242856 | c.-377C>T | upstream_gene_variant | 0.93 |
| embA | 4242862 | c.-371A>G | upstream_gene_variant | 0.91 |
| embC | 4242863 | p.Tyr1001Asn | missense_variant | 0.91 |
| embC | 4242878 | p.Thr1006Ala | missense_variant | 1.0 |
| embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.8 |
| embC | 4242885 | p.Lys1008Arg | missense_variant | 0.8 |
| embA | 4242892 | c.-341G>C | upstream_gene_variant | 0.83 |
| embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.83 |
| embA | 4242919 | c.-314A>G | upstream_gene_variant | 0.75 |
| embA | 4242928 | c.-305A>C | upstream_gene_variant | 0.8 |
| embA | 4242931 | c.-302G>C | upstream_gene_variant | 0.8 |
| embA | 4242940 | c.-293T>C | upstream_gene_variant | 0.75 |
| embC | 4242941 | p.His1027Asn | missense_variant | 0.75 |
| embA | 4242946 | c.-287T>C | upstream_gene_variant | 0.75 |
| embA | 4242952 | c.-281T>C | upstream_gene_variant | 1.0 |
| embC | 4242965 | p.Ile1035Val | missense_variant | 1.0 |
| embA | 4242974 | c.-259C>T | upstream_gene_variant | 1.0 |
| embA | 4243248 | p.Asn6Glu | missense_variant | 1.0 |
| embA | 4243259 | c.27T>G | synonymous_variant | 1.0 |
| embA | 4244213 | c.981C>G | synonymous_variant | 1.0 |
| embA | 4244219 | c.987C>G | synonymous_variant | 1.0 |
| embA | 4244228 | c.996A>C | synonymous_variant | 1.0 |
| embA | 4244241 | c.1009C>T | synonymous_variant | 1.0 |
| embA | 4244247 | p.Val339Ile | missense_variant | 1.0 |
| embA | 4244254 | p.Arg341His | missense_variant | 1.0 |
| embA | 4244257 | p.Phe342Trp | missense_variant | 1.0 |
| embA | 4244270 | c.1038G>C | synonymous_variant | 1.0 |
| embA | 4244276 | c.1044A>G | synonymous_variant | 1.0 |
| embA | 4244283 | p.Pro351Lys | missense_variant | 1.0 |
| embA | 4244291 | c.1059G>C | synonymous_variant | 1.0 |
| embA | 4244298 | p.Ser356Ala | missense_variant | 1.0 |
| embA | 4244309 | c.1077C>G | synonymous_variant | 1.0 |
| embA | 4244312 | c.1080T>G | synonymous_variant | 1.0 |
| embA | 4244315 | c.1083G>C | synonymous_variant | 1.0 |
| embA | 4244317 | p.Phe362Cys | missense_variant | 0.94 |
| embA | 4244324 | c.1092T>G | synonymous_variant | 1.0 |
| embA | 4244327 | c.1095T>C | synonymous_variant | 1.0 |
| embA | 4244337 | p.Leu369Val | missense_variant | 1.0 |
| embA | 4244340 | p.Ser370Ala | missense_variant | 1.0 |
| embA | 4244345 | c.1113C>G | synonymous_variant | 1.0 |
| embA | 4244372 | c.1140T>G | synonymous_variant | 1.0 |
| embA | 4244378 | c.1146G>A | synonymous_variant | 1.0 |
| embA | 4244390 | c.1158G>C | synonymous_variant | 1.0 |
| embA | 4244657 | c.1425G>C | synonymous_variant | 0.5 |
| embA | 4244666 | c.1434G>C | synonymous_variant | 0.57 |
| embA | 4244669 | c.1437G>C | synonymous_variant | 0.57 |
| embA | 4244675 | c.1443A>G | synonymous_variant | 0.57 |
| embA | 4244681 | c.1449A>G | synonymous_variant | 0.8 |
| embA | 4244705 | c.1473G>C | synonymous_variant | 1.0 |
| embA | 4244708 | c.1476C>G | synonymous_variant | 1.0 |
| embA | 4244714 | c.1482C>G | synonymous_variant | 1.0 |
| embA | 4244720 | c.1488C>T | synonymous_variant | 1.0 |
| embA | 4244728 | p.Phe499Trp | missense_variant | 1.0 |
| embA | 4245032 | c.1800A>G | synonymous_variant | 0.5 |
| embA | 4245041 | c.1809C>G | synonymous_variant | 0.95 |
| embA | 4245060 | c.1828T>C | synonymous_variant | 1.0 |
| embA | 4245078 | p.Trp616Val | missense_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245093 | p.Ile621Val | missense_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245136 | p.Tyr635Trp | missense_variant | 1.0 |
| embA | 4245152 | c.1920C>G | synonymous_variant | 1.0 |
| embA | 4245173 | c.1941G>C | synonymous_variant | 1.0 |
| embA | 4245174 | p.Ser648Thr | missense_variant | 1.0 |
| embA | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Ala | missense_variant | 1.0 |
| embA | 4245206 | c.1974A>G | synonymous_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>C | synonymous_variant | 1.0 |
| embA | 4245222 | p.Tyr664Gln | missense_variant | 1.0 |
| embA | 4245248 | c.2016G>C | synonymous_variant | 0.94 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 0.93 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 0.91 |
| embA | 4245281 | c.2049C>G | synonymous_variant | 0.5 |
| embA | 4245368 | c.2136T>C | synonymous_variant | 0.67 |
| embA | 4245377 | c.2145T>C | synonymous_variant | 0.85 |
| embA | 4245388 | p.Ala719Gly | missense_variant | 0.87 |
| embA | 4245398 | c.2166C>T | synonymous_variant | 0.9 |
| embA | 4245402 | p.Thr724Ala | missense_variant | 0.95 |
| embA | 4245408 | p.Leu726Ile | missense_variant | 0.95 |
| embA | 4245412 | p.Ser727Thr | missense_variant | 0.95 |
| embA | 4245414 | p.Thr728Ser | missense_variant | 0.95 |
| embA | 4245424 | c.2193_2194insCCGAGC | conservative_inframe_insertion | 0.95 |
| embA | 4245431 | c.2199T>C | synonymous_variant | 0.95 |
| embA | 4245458 | c.2226G>A | synonymous_variant | 0.94 |
| embA | 4245461 | c.2229C>G | synonymous_variant | 0.93 |
| embA | 4245467 | c.2235C>G | synonymous_variant | 0.92 |
| embA | 4245470 | c.2238T>C | synonymous_variant | 1.0 |
| embA | 4245736 | p.Ala835Val | missense_variant | 1.0 |
| embB | 4245740 | c.-774T>C | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 1.0 |
| embA | 4245771 | p.Asn847Ala | missense_variant | 1.0 |
| embB | 4245785 | c.-729G>C | upstream_gene_variant | 1.0 |
| embB | 4245791 | c.-723C>G | upstream_gene_variant | 0.93 |
| embA | 4245795 | p.Ala855Ser | missense_variant | 0.93 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.93 |
| embB | 4245818 | c.-696C>G | upstream_gene_variant | 0.83 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 0.83 |
| embA | 4245822 | p.Pro864Ala | missense_variant | 0.83 |
| embA | 4245834 | p.Leu868Ile | missense_variant | 0.8 |
| embB | 4245839 | c.-675G>C | upstream_gene_variant | 0.8 |
| embB | 4245842 | c.-672G>C | upstream_gene_variant | 0.8 |
| embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.82 |
| embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.85 |
| embB | 4245875 | c.-639G>A | upstream_gene_variant | 0.8 |
| embA | 4245885 | p.Asp885Thr | missense_variant | 0.78 |
| embA | 4245892 | p.Ile887Thr | missense_variant | 0.88 |
| embB | 4245899 | c.-615C>G | upstream_gene_variant | 0.88 |
| embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.88 |
| embB | 4245917 | c.-597G>A | upstream_gene_variant | 1.0 |
| embA | 4245930 | p.Gly900Arg | missense_variant | 1.0 |
| embB | 4245935 | c.-579G>C | upstream_gene_variant | 1.0 |
| embA | 4245942 | p.Arg904Ser | missense_variant | 1.0 |
| embA | 4245946 | p.Ile905Thr | missense_variant | 1.0 |
| embB | 4245971 | c.-543G>C | upstream_gene_variant | 1.0 |
| embB | 4245983 | c.-531A>T | upstream_gene_variant | 1.0 |
| embA | 4245987 | p.Gln919Glu | missense_variant | 1.0 |
| embB | 4245992 | c.-522C>G | upstream_gene_variant | 1.0 |
| embB | 4246004 | c.-510T>C | upstream_gene_variant | 1.0 |
| embB | 4246013 | c.-501T>C | upstream_gene_variant | 0.96 |
| embA | 4246020 | p.Ala930Thr | missense_variant | 1.0 |
| embA | 4246041 | p.Asp937Asn | missense_variant | 1.0 |
| embB | 4246055 | c.-459T>C | upstream_gene_variant | 1.0 |
| embB | 4246064 | c.-450T>C | upstream_gene_variant | 1.0 |
| embA | 4246080 | p.Pro950Ser | missense_variant | 0.92 |
| embA | 4246085 | p.Glu951Asp | missense_variant | 0.91 |
| embB | 4246088 | c.-426A>G | upstream_gene_variant | 0.91 |
| embB | 4246097 | c.-417C>G | upstream_gene_variant | 0.9 |
| embB | 4246103 | c.-411C>G | upstream_gene_variant | 0.89 |
| embB | 4246109 | c.-405C>G | upstream_gene_variant | 0.89 |
| embB | 4246115 | c.-399T>C | upstream_gene_variant | 0.88 |
| embB | 4246163 | c.-351G>C | upstream_gene_variant | 0.6 |
| embB | 4246164 | c.-350T>C | upstream_gene_variant | 0.6 |
| embB | 4246184 | c.-330A>C | upstream_gene_variant | 1.0 |
| embB | 4246187 | c.-327C>G | upstream_gene_variant | 1.0 |
| embB | 4246196 | c.-318C>G | upstream_gene_variant | 1.0 |
| embB | 4246205 | c.-309A>G | upstream_gene_variant | 1.0 |
| embB | 4246211 | c.-303T>C | upstream_gene_variant | 1.0 |
| embB | 4246217 | c.-297G>A | upstream_gene_variant | 1.0 |
| embB | 4246220 | c.-294T>C | upstream_gene_variant | 1.0 |
| embA | 4246227 | p.Ile999Val | missense_variant | 1.0 |
| embB | 4246238 | c.-276T>G | upstream_gene_variant | 1.0 |
| embB | 4246244 | c.-270G>A | upstream_gene_variant | 1.0 |
| embB | 4246250 | c.-264G>A | upstream_gene_variant | 1.0 |
| embB | 4246259 | c.-255G>C | upstream_gene_variant | 1.0 |
| embB | 4246274 | c.-240G>C | upstream_gene_variant | 1.0 |
| embA | 4246290 | p.Leu1020Gly | missense_variant | 1.0 |
| embA | 4246299 | p.Ser1023Ala | missense_variant | 1.0 |
| embA | 4246305 | p.Ser1025Glu | missense_variant | 1.0 |
| embB | 4246316 | c.-198T>C | upstream_gene_variant | 1.0 |
| embA | 4246326 | p.Phe1032Val | missense_variant | 1.0 |
| embA | 4246335 | p.Ala1035Thr | missense_variant | 1.0 |
| embA | 4246338 | p.Leu1036Met | missense_variant | 1.0 |
| embB | 4246352 | c.-162G>C | upstream_gene_variant | 1.0 |
| embB | 4246364 | c.-150G>C | upstream_gene_variant | 1.0 |
| embB | 4246373 | c.-141T>G | upstream_gene_variant | 1.0 |
| embB | 4246376 | c.-138G>T | upstream_gene_variant | 1.0 |
| embA | 4246401 | p.Val1057Ile | missense_variant | 1.0 |
| embA | 4246407 | p.Gln1059Lys | missense_variant | 1.0 |
| embA | 4246413 | p.His1061Tyr | missense_variant | 1.0 |
| embA | 4246417 | p.Arg1062Pro | missense_variant | 1.0 |
| embB | 4246427 | c.-87G>C | upstream_gene_variant | 1.0 |
| embB | 4246433 | c.-81T>C | upstream_gene_variant | 1.0 |
| embB | 4246600 | c.87G>C | synonymous_variant | 0.5 |
| embB | 4246621 | c.108T>C | synonymous_variant | 1.0 |
| embB | 4246627 | c.114T>C | synonymous_variant | 1.0 |
| embB | 4246628 | p.Val39Leu | missense_variant | 1.0 |
| embB | 4246631 | c.118T>C | synonymous_variant | 1.0 |
| embB | 4246637 | p.Val42Ile | missense_variant | 1.0 |
| embB | 4246961 | p.Val150Ile | missense_variant | 1.0 |
| embB | 4246969 | c.456T>C | synonymous_variant | 1.0 |
| embB | 4246975 | p.His154Gln | missense_variant | 1.0 |
| embB | 4246982 | p.Thr157Ala | missense_variant | 1.0 |
| embB | 4246990 | c.477C>G | synonymous_variant | 1.0 |
| embB | 4246992 | p.Asn160Thr | missense_variant | 1.0 |
| embB | 4247005 | c.492C>G | synonymous_variant | 1.0 |
| embB | 4247007 | p.Lys165Thr | missense_variant | 1.0 |
| embB | 4247015 | p.Ser168Val | missense_variant | 1.0 |
| embB | 4247021 | p.Ala170Arg | missense_variant | 1.0 |
| embB | 4247027 | p.Leu172Val | missense_variant | 1.0 |
| embB | 4247033 | p.Ser174Gly | missense_variant | 0.96 |
| embB | 4247068 | c.555T>C | synonymous_variant | 1.0 |
| embB | 4247086 | c.573C>T | synonymous_variant | 1.0 |
| embB | 4247098 | c.585C>G | synonymous_variant | 1.0 |
| embB | 4247104 | c.591G>C | synonymous_variant | 1.0 |
| embB | 4247105 | p.Pro198Ala | missense_variant | 1.0 |
| embB | 4247110 | c.597G>C | synonymous_variant | 1.0 |
| embB | 4247113 | c.600G>C | synonymous_variant | 1.0 |
| embB | 4247114 | p.Ala201Lys | missense_variant | 1.0 |
| embB | 4247117 | p.Val202Leu | missense_variant | 1.0 |
| embB | 4247125 | c.612G>C | synonymous_variant | 1.0 |
| embB | 4247150 | p.Arg213Thr | missense_variant | 0.92 |
| embB | 4247167 | c.654A>G | synonymous_variant | 0.9 |
| embB | 4247317 | c.804G>C | synonymous_variant | 0.67 |
| embB | 4247320 | c.807T>C | synonymous_variant | 0.5 |
| embB | 4247326 | c.813A>C | synonymous_variant | 0.62 |
| embB | 4247328 | p.Ser272Asn | missense_variant | 0.78 |
| embB | 4247337 | p.Thr275Lys | missense_variant | 0.83 |
| embB | 4247348 | p.Thr279Ala | missense_variant | 0.85 |
| embB | 4247357 | p.Val282Thr | missense_variant | 0.86 |
| embB | 4247365 | c.852A>C | synonymous_variant | 0.91 |
| embB | 4247371 | c.858C>G | synonymous_variant | 0.94 |
| embB | 4247375 | p.Leu288Val | missense_variant | 0.94 |
| embB | 4247380 | c.867C>G | synonymous_variant | 0.95 |
| embB | 4247386 | c.873T>C | synonymous_variant | 0.96 |
| embB | 4247395 | c.882C>G | synonymous_variant | 0.96 |
| embB | 4247401 | c.888T>C | synonymous_variant | 0.96 |
| embB | 4247437 | c.924A>G | synonymous_variant | 0.99 |
| embB | 4247443 | c.930C>G | synonymous_variant | 0.99 |
| embB | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247528 | p.Leu339Tyr | missense_variant | 1.0 |
| embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
| embB | 4247551 | c.1038C>G | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247566 | c.1053C>G | synonymous_variant | 1.0 |
| embB | 4247567 | c.1054C>T | synonymous_variant | 1.0 |
| embB | 4247572 | c.1059A>G | synonymous_variant | 1.0 |
| embB | 4247578 | c.1065G>C | synonymous_variant | 1.0 |
| embB | 4247579 | p.Ala356Ile | missense_variant | 1.0 |
| embB | 4247591 | p.Val360Leu | missense_variant | 1.0 |
| embB | 4247608 | c.1095G>C | synonymous_variant | 1.0 |
| embB | 4247611 | c.1098G>C | synonymous_variant | 1.0 |
| embB | 4247689 | c.1176G>C | synonymous_variant | 1.0 |
| embB | 4247692 | c.1179C>G | synonymous_variant | 1.0 |
| embB | 4247695 | c.1182G>C | synonymous_variant | 1.0 |
| embB | 4247716 | c.1203C>G | synonymous_variant | 1.0 |
| embB | 4247722 | c.1209G>C | synonymous_variant | 1.0 |
| embB | 4247725 | c.1212G>C | synonymous_variant | 1.0 |
| embB | 4247729 | p.Gly406Pro | missense_variant | 1.0 |
| embB | 4247740 | c.1227G>C | synonymous_variant | 1.0 |
| embB | 4247746 | c.1233C>G | synonymous_variant | 1.0 |
| embB | 4247761 | c.1248T>C | synonymous_variant | 0.97 |
| embB | 4247785 | c.1272G>C | synonymous_variant | 0.98 |
| embB | 4247797 | c.1284C>G | synonymous_variant | 0.97 |
| embB | 4247800 | c.1287A>G | synonymous_variant | 0.97 |
| embB | 4247803 | c.1290G>C | synonymous_variant | 0.97 |
| embB | 4247819 | p.Val436Ile | missense_variant | 0.97 |
| embB | 4247827 | c.1314C>G | synonymous_variant | 0.95 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 0.93 |
| embB | 4247836 | c.1323A>C | synonymous_variant | 0.9 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 0.9 |
| embB | 4247842 | c.1329T>C | synonymous_variant | 0.9 |
| embB | 4247869 | c.1356G>C | synonymous_variant | 0.87 |
| embB | 4247881 | c.1368G>C | synonymous_variant | 0.83 |
| embB | 4247896 | c.1383G>C | synonymous_variant | 0.76 |
| embB | 4247899 | p.Met462Ile | missense_variant | 0.76 |
| embB | 4247905 | c.1392G>C | synonymous_variant | 0.75 |
| embB | 4247909 | c.1396T>C | synonymous_variant | 0.71 |
| embB | 4247914 | c.1401G>A | synonymous_variant | 0.71 |
| embB | 4247917 | c.1404C>G | synonymous_variant | 0.71 |
| embB | 4247920 | c.1407T>C | synonymous_variant | 0.71 |
| embB | 4247923 | c.1410T>C | synonymous_variant | 0.71 |
| embB | 4247938 | c.1425G>C | synonymous_variant | 0.93 |
| embB | 4247940 | p.Leu476Trp | missense_variant | 0.92 |
| embB | 4247945 | c.1432T>C | synonymous_variant | 0.92 |
| embB | 4247951 | p.Ser480Ala | missense_variant | 0.89 |
| embB | 4247972 | p.Thr487Phe | missense_variant | 0.88 |
| embB | 4247992 | c.1479G>C | synonymous_variant | 0.91 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 0.93 |
| embB | 4248008 | c.1495C>T | synonymous_variant | 0.93 |
| embB | 4248013 | c.1500A>G | synonymous_variant | 0.93 |
| embB | 4248025 | c.1512A>G | synonymous_variant | 0.88 |
| embB | 4248035 | p.Val508Ile | missense_variant | 0.88 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 0.88 |
| embB | 4248044 | p.Lys511Ala | missense_variant | 0.88 |
| embB | 4248055 | c.1542G>C | synonymous_variant | 0.88 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 0.88 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248097 | c.1584C>G | synonymous_variant | 1.0 |
| embB | 4248106 | c.1593C>G | synonymous_variant | 1.0 |
| embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
| embB | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>G | synonymous_variant | 1.0 |
| embB | 4248139 | c.1626C>G | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248149 | p.Thr546Ala | missense_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248169 | c.1656C>G | synonymous_variant | 1.0 |
| embB | 4248170 | p.Ala553Ser | missense_variant | 1.0 |
| embB | 4248173 | p.Val554Met | missense_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>G | synonymous_variant | 1.0 |
| embB | 4248223 | c.1710G>C | synonymous_variant | 1.0 |
| embB | 4248266 | c.1753C>T | synonymous_variant | 0.99 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248313 | c.1800C>G | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248322 | c.1809G>C | synonymous_variant | 1.0 |
| embB | 4248328 | c.1815G>C | synonymous_variant | 1.0 |
| embB | 4248346 | c.1833G>C | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4248355 | c.1842A>G | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 1.0 |
| embB | 4248360 | p.Pro616His | missense_variant | 1.0 |
| embB | 4248362 | p.Ser617Glu | missense_variant | 1.0 |
| embB | 4248366 | p.Val618Ala | missense_variant | 1.0 |
| embB | 4248373 | c.1860C>G | synonymous_variant | 1.0 |
| embB | 4248407 | c.1894_1896delTTAinsCTG | synonymous_variant | 1.0 |
| embB | 4248410 | p.Phe633Leu | missense_variant | 1.0 |
| embB | 4248416 | p.Leu635Val | missense_variant | 1.0 |
| embB | 4248425 | c.1912T>C | synonymous_variant | 1.0 |
| embB | 4248430 | c.1917T>C | synonymous_variant | 1.0 |
| embB | 4248432 | p.Trp640Phe | missense_variant | 1.0 |
| embB | 4248457 | c.1944T>C | synonymous_variant | 1.0 |
| embB | 4248463 | c.1950C>G | synonymous_variant | 1.0 |
| embB | 4248472 | c.1959T>C | synonymous_variant | 1.0 |
| embB | 4248475 | c.1962G>C | synonymous_variant | 1.0 |
| embB | 4248490 | c.1977G>C | synonymous_variant | 1.0 |
| embB | 4248500 | p.Ile663Val | missense_variant | 1.0 |
| embB | 4248504 | p.Asp664Ala | missense_variant | 1.0 |
| embB | 4248508 | c.1995G>A | synonymous_variant | 1.0 |
| embB | 4248512 | p.Thr667Ser | missense_variant | 1.0 |
| embB | 4248515 | p.Val668Ile | missense_variant | 1.0 |
| embB | 4248714 | p.Ser734Tyr | missense_variant | 0.67 |
| embB | 4249069 | c.2556A>C | synonymous_variant | 1.0 |
| embB | 4249082 | p.Thr857Arg | missense_variant | 1.0 |
| embB | 4249087 | c.2574C>G | synonymous_variant | 1.0 |
| embB | 4249088 | p.Val859Thr | missense_variant | 1.0 |
| embB | 4249102 | c.2589T>C | synonymous_variant | 1.0 |
| embB | 4249104 | p.Leu864Gln | missense_variant | 1.0 |
| embB | 4249112 | p.Lys867Arg | missense_variant | 1.0 |
| embB | 4249117 | c.2604G>C | synonymous_variant | 1.0 |
| embB | 4249122 | p.Asp870Ala | missense_variant | 1.0 |
| embB | 4249132 | c.2619G>C | synonymous_variant | 1.0 |
| embB | 4249153 | c.2640G>C | synonymous_variant | 1.0 |
| embB | 4249255 | c.2742G>C | synonymous_variant | 1.0 |
| embB | 4249259 | p.Met916Leu | missense_variant | 1.0 |
| embB | 4249268 | p.Asp919Tyr | missense_variant | 1.0 |
| embB | 4249276 | c.2763A>G | synonymous_variant | 1.0 |
| embB | 4249282 | c.2769A>G | synonymous_variant | 1.0 |
| embB | 4249296 | p.Ala928Val | missense_variant | 1.0 |
| embB | 4249321 | c.2808A>C | synonymous_variant | 1.0 |
| embB | 4249322 | p.Ala937Ser | missense_variant | 1.0 |
| embB | 4249325 | p.Lys938Gln | missense_variant | 1.0 |
| embB | 4249339 | c.2826T>C | synonymous_variant | 1.0 |
| embB | 4249342 | c.2829C>G | synonymous_variant | 1.0 |
| embB | 4249348 | c.2835G>C | synonymous_variant | 1.0 |
| embB | 4249360 | c.2847G>C | synonymous_variant | 1.0 |
| embB | 4249369 | c.2856T>C | synonymous_variant | 1.0 |
| embB | 4249381 | c.2868A>G | synonymous_variant | 1.0 |
| embB | 4249387 | p.Glu958Asp | missense_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249420 | c.2907G>C | synonymous_variant | 1.0 |
| embB | 4249423 | p.Asp970Glu | missense_variant | 1.0 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 1.0 |
| embB | 4249441 | c.2928A>G | synonymous_variant | 1.0 |
| embB | 4249444 | c.2931T>C | synonymous_variant | 1.0 |
| embB | 4249447 | c.2934G>C | synonymous_variant | 1.0 |
| embB | 4249469 | p.Leu986Met | missense_variant | 1.0 |
| embB | 4249483 | c.2970C>G | synonymous_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 1.0 |
| embB | 4249492 | c.2979C>G | synonymous_variant | 1.0 |
| embB | 4249498 | c.2985G>C | synonymous_variant | 1.0 |
| embB | 4249507 | p.Gln998His | missense_variant | 1.0 |
| embB | 4249521 | p.Ala1003Val | missense_variant | 1.0 |
| embB | 4249525 | c.3012T>C | synonymous_variant | 1.0 |
| embB | 4249529 | p.Ile1006Val | missense_variant | 1.0 |
| embB | 4249532 | p.Ala1007Thr | missense_variant | 1.0 |
| embB | 4249537 | c.3024A>G | synonymous_variant | 1.0 |
| embB | 4249543 | c.3030G>C | synonymous_variant | 1.0 |
| embB | 4249558 | c.3045A>C | synonymous_variant | 1.0 |
| aftB | 4267304 | p.Val511Ala | missense_variant | 0.67 |
| aftB | 4267310 | c.1527G>C | synonymous_variant | 0.67 |
| aftB | 4267316 | c.1521A>G | synonymous_variant | 0.5 |
| aftB | 4267334 | c.1503T>C | synonymous_variant | 0.5 |
| aftB | 4267354 | p.Gly495Ser | missense_variant | 0.4 |
| aftB | 4267355 | p.Leu494Val | missense_variant | 0.4 |
| aftB | 4267364 | p.Met491Leu | missense_variant | 0.4 |
| aftB | 4267382 | c.1455A>C | synonymous_variant | 0.5 |
| aftB | 4267550 | c.1287C>T | synonymous_variant | 1.0 |
| aftB | 4267559 | c.1278C>G | synonymous_variant | 1.0 |
| aftB | 4267571 | c.1266T>C | synonymous_variant | 1.0 |
| aftB | 4267574 | c.1263G>C | synonymous_variant | 1.0 |
| aftB | 4267577 | c.1260C>T | synonymous_variant | 1.0 |
| aftB | 4267580 | c.1257G>C | synonymous_variant | 1.0 |
| aftB | 4267583 | c.1254C>G | synonymous_variant | 1.0 |
| aftB | 4267604 | c.1233C>T | synonymous_variant | 1.0 |
| aftB | 4267619 | c.1218C>G | synonymous_variant | 1.0 |
| aftB | 4267622 | p.Ser405Thr | missense_variant | 1.0 |
| aftB | 4267625 | c.1212T>C | synonymous_variant | 1.0 |
| aftB | 4267634 | p.Arg401His | missense_variant | 1.0 |
| aftB | 4267649 | c.1188T>C | synonymous_variant | 0.93 |
| aftB | 4267654 | p.Met395Leu | missense_variant | 0.92 |
| aftB | 4267661 | c.1176G>C | synonymous_variant | 0.91 |
| aftB | 4267667 | c.1170A>G | synonymous_variant | 0.67 |
| aftB | 4268068 | p.Val257Leu | missense_variant | 1.0 |
| aftB | 4268077 | p.Met254Leu | missense_variant | 1.0 |
| aftB | 4268081 | c.756A>G | synonymous_variant | 1.0 |
| aftB | 4268099 | c.738G>C | synonymous_variant | 1.0 |
| aftB | 4268105 | c.732T>C | synonymous_variant | 1.0 |
| aftB | 4268117 | c.720G>C | synonymous_variant | 1.0 |
| aftB | 4268123 | p.Ser238Gly | missense_variant | 1.0 |
| aftB | 4268126 | c.711G>C | synonymous_variant | 1.0 |
| aftB | 4268129 | c.708T>G | synonymous_variant | 1.0 |
| aftB | 4268138 | c.699A>G | synonymous_variant | 0.98 |
| aftB | 4268144 | c.693T>C | synonymous_variant | 0.98 |
| aftB | 4268168 | c.669C>G | synonymous_variant | 0.98 |
| aftB | 4268179 | c.658T>C | synonymous_variant | 0.97 |
| aftB | 4268180 | p.Phe219Leu | missense_variant | 0.97 |
| aftB | 4268183 | c.654A>C | synonymous_variant | 0.97 |
| aftB | 4268189 | c.648C>G | synonymous_variant | 0.97 |
| aftB | 4268205 | p.Val211Ala | missense_variant | 0.95 |
| aftB | 4268207 | c.630C>G | synonymous_variant | 0.94 |
| aftB | 4268213 | c.624T>G | synonymous_variant | 0.94 |
| aftB | 4268225 | c.612G>C | synonymous_variant | 0.94 |
| aftB | 4268234 | c.601_603delTTGinsCTC | synonymous_variant | 0.88 |
| aftB | 4268638 | p.Leu67Met | missense_variant | 1.0 |
| aftB | 4268645 | c.192G>C | synonymous_variant | 1.0 |
| aftB | 4268654 | c.183A>G | synonymous_variant | 1.0 |
| aftB | 4268657 | c.180G>C | synonymous_variant | 1.0 |
| aftB | 4268666 | c.171G>C | synonymous_variant | 1.0 |
| aftB | 4268669 | c.168A>G | synonymous_variant | 1.0 |
| aftB | 4268672 | c.165C>A | synonymous_variant | 1.0 |
| aftB | 4268675 | c.162A>G | synonymous_variant | 1.0 |
| aftB | 4268696 | c.141G>C | synonymous_variant | 1.0 |
| aftB | 4268699 | c.138A>C | synonymous_variant | 1.0 |
| aftB | 4269006 | c.-170T>C | upstream_gene_variant | 1.0 |
| aftB | 4269009 | c.-173A>G | upstream_gene_variant | 1.0 |
| aftB | 4269012 | c.-176G>C | upstream_gene_variant | 1.0 |
| aftB | 4269015 | c.-179G>A | upstream_gene_variant | 1.0 |
| aftB | 4269018 | c.-182G>C | upstream_gene_variant | 1.0 |
| aftB | 4269027 | c.-191C>G | upstream_gene_variant | 1.0 |
| aftB | 4269033 | c.-197T>C | upstream_gene_variant | 1.0 |
| aftB | 4269036 | c.-200C>G | upstream_gene_variant | 1.0 |
| aftB | 4269051 | c.-215C>G | upstream_gene_variant | 1.0 |
| aftB | 4269072 | c.-236G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |
| ubiA | 4269083 | p.Ser251Thr | missense_variant | 1.0 |
| ubiA | 4269091 | p.Phe248Tyr | missense_variant | 1.0 |
| ubiA | 4269097 | p.Ser246Cys | missense_variant | 1.0 |
| aftB | 4269123 | c.-287T>G | upstream_gene_variant | 1.0 |
| aftB | 4269132 | c.-296G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269141 | p.Leu231Val | missense_variant | 1.0 |
| aftB | 4269144 | c.-308C>G | upstream_gene_variant | 1.0 |
| aftB | 4269156 | c.-320C>G | upstream_gene_variant | 1.0 |
| aftB | 4269171 | c.-335C>G | upstream_gene_variant | 1.0 |
| aftB | 4269186 | c.-350C>G | upstream_gene_variant | 1.0 |
| aftB | 4269201 | c.-365A>G | upstream_gene_variant | 1.0 |
| aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.98 |
| aftB | 4269222 | c.-386T>G | upstream_gene_variant | 1.0 |
| aftB | 4269242 | c.-406C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| aftB | 4269252 | c.-416C>G | upstream_gene_variant | 1.0 |
| aftB | 4269281 | c.-445C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269380 | p.Val152Ile | missense_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| ubiA | 4269392 | p.Val148Leu | missense_variant | 1.0 |
| aftB | 4269402 | c.-566T>C | upstream_gene_variant | 1.0 |
| aftB | 4269405 | c.-569G>A | upstream_gene_variant | 1.0 |
| aftB | 4269411 | c.-575T>C | upstream_gene_variant | 1.0 |
| aftB | 4269414 | c.-578T>C | upstream_gene_variant | 1.0 |
| aftB | 4269420 | c.-584T>C | upstream_gene_variant | 1.0 |
| aftB | 4269428 | c.-592T>C | upstream_gene_variant | 1.0 |
| aftB | 4269435 | c.-599C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269440 | p.Leu132Ile | missense_variant | 1.0 |
| ubiA | 4269448 | p.Val129Ala | missense_variant | 1.0 |
| aftB | 4269453 | c.-617A>G | upstream_gene_variant | 1.0 |
| aftB | 4269459 | c.-623G>A | upstream_gene_variant | 1.0 |
| aftB | 4269528 | c.-692G>C | upstream_gene_variant | 1.0 |
| aftB | 4269540 | c.-704C>G | upstream_gene_variant | 1.0 |
| aftB | 4269543 | c.-707G>C | upstream_gene_variant | 1.0 |
| aftB | 4269552 | c.-716C>G | upstream_gene_variant | 1.0 |
| aftB | 4269555 | c.-719C>G | upstream_gene_variant | 1.0 |
| aftB | 4269564 | c.-728G>A | upstream_gene_variant | 1.0 |
| aftB | 4269573 | c.-737A>G | upstream_gene_variant | 1.0 |
| aftB | 4269594 | c.-758A>C | upstream_gene_variant | 1.0 |
| aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
| aftB | 4269612 | c.-776T>C | upstream_gene_variant | 1.0 |
| aftB | 4269621 | c.-785C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269627 | p.Val69Ile | missense_variant | 1.0 |
| ubiA | 4269632 | p.Ala68Ser | missense_variant | 1.0 |
| aftB | 4269636 | c.-800C>A | upstream_gene_variant | 1.0 |
| aftB | 4269639 | c.-803C>G | upstream_gene_variant | 1.0 |
| aftB | 4269660 | c.-824C>G | upstream_gene_variant | 1.0 |
| ethA | 4326292 | c.1182G>A | synonymous_variant | 1.0 |
| ethA | 4326304 | c.1170C>G | synonymous_variant | 1.0 |
| ethA | 4326307 | c.1167C>G | synonymous_variant | 1.0 |
| ethA | 4326310 | c.1164T>C | synonymous_variant | 1.0 |
| ethA | 4328461 | c.-989_-988delCCinsTG | upstream_gene_variant | 1.0 |
| ethA | 4328464 | c.-991C>G | upstream_gene_variant | 1.0 |
| ethA | 4328467 | c.-994G>T | upstream_gene_variant | 1.0 |
| ethA | 4328470 | c.-998_-997delAGinsGA | upstream_gene_variant | 1.0 |
| gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
| gid | 4407622 | p.Asn194Thr | missense_variant | 0.5 |
| gid | 4407646 | p.Val186Ala | missense_variant | 0.5 |
| gid | 4407653 | p.Val184Ile | missense_variant | 0.5 |
| gid | 4407654 | c.549G>C | synonymous_variant | 0.5 |
| gid | 4407663 | c.540A>G | synonymous_variant | 0.5 |
| gid | 4407666 | p.Ile179Glu | missense_variant | 0.5 |
