Run ID: ERR212123
Sample name:
Date: 31-03-2023 15:48:09
Number of reads: 688836
Percentage reads mapped: 17.41
Strain:
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.99 | streptomycin |
| embB | 4248488 | p.Ala659Thr | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6049 | c.810G>A | synonymous_variant | 1.0 |
| gyrB | 6055 | c.816T>C | synonymous_variant | 1.0 |
| gyrB | 6067 | c.828G>C | synonymous_variant | 1.0 |
| gyrB | 6076 | c.837C>G | synonymous_variant | 1.0 |
| gyrB | 6085 | c.846C>T | synonymous_variant | 1.0 |
| gyrB | 6086 | p.Thr283Glu | missense_variant | 1.0 |
| gyrB | 6091 | c.852G>C | synonymous_variant | 1.0 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 1.0 |
| gyrB | 6109 | c.870G>A | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6124 | c.885C>A | synonymous_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6145 | c.906C>T | synonymous_variant | 1.0 |
| gyrB | 6160 | c.921C>G | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>G | synonymous_variant | 1.0 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
| gyrB | 6209 | c.970C>T | synonymous_variant | 1.0 |
| gyrB | 6214 | c.975G>A | synonymous_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
| gyrB | 6298 | c.1059C>T | synonymous_variant | 0.98 |
| gyrA | 6307 | c.-995T>C | upstream_gene_variant | 1.0 |
| gyrA | 6310 | c.-992G>C | upstream_gene_variant | 1.0 |
| gyrA | 6331 | c.-971A>G | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6376 | c.-926G>A | upstream_gene_variant | 1.0 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 1.0 |
| gyrA | 6415 | c.-887G>C | upstream_gene_variant | 1.0 |
| gyrA | 6427 | c.-875T>C | upstream_gene_variant | 1.0 |
| gyrA | 6439 | c.-863C>G | upstream_gene_variant | 1.0 |
| gyrA | 6515 | c.-787T>C | upstream_gene_variant | 1.0 |
| gyrA | 6523 | c.-779G>T | upstream_gene_variant | 1.0 |
| gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.75 |
| gyrB | 6531 | p.Ser431Thr | missense_variant | 0.75 |
| gyrA | 6547 | c.-755T>C | upstream_gene_variant | 0.67 |
| gyrA | 6556 | c.-746C>G | upstream_gene_variant | 0.67 |
| gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.67 |
| gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.5 |
| gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.5 |
| gyrA | 6589 | c.-713G>A | upstream_gene_variant | 0.5 |
| gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.6 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.6 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.6 |
| gyrA | 6619 | c.-683T>G | upstream_gene_variant | 0.6 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 0.6 |
| gyrA | 6625 | c.-677G>A | upstream_gene_variant | 0.75 |
| gyrA | 6631 | c.-671C>T | upstream_gene_variant | 0.75 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.75 |
| gyrA | 6637 | c.-665T>C | upstream_gene_variant | 0.75 |
| gyrA | 6640 | c.-662A>G | upstream_gene_variant | 0.75 |
| gyrA | 6649 | c.-653T>G | upstream_gene_variant | 0.8 |
| gyrA | 6652 | c.-650C>G | upstream_gene_variant | 0.83 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.88 |
| gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.94 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.95 |
| gyrA | 6679 | c.-623G>T | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | 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 | 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 | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>A | upstream_gene_variant | 1.0 |
| 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 | 6865 | c.-437G>C | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430_-428delTTGinsCTC | 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 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | 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 | 6964 | c.-338C>T | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrA | 6970 | c.-332C>T | 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 | 6997 | c.-305G>A | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>C | upstream_gene_variant | 1.0 |
| gyrA | 7018 | c.-284G>T | upstream_gene_variant | 1.0 |
| gyrA | 7024 | c.-278G>C | upstream_gene_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_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>G | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>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 | 7129 | c.-173T>C | 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 | 0.92 |
| gyrA | 7150 | c.-152G>C | upstream_gene_variant | 0.92 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 0.93 |
| gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.94 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.93 |
| gyrA | 7189 | c.-113C>T | upstream_gene_variant | 0.92 |
| gyrA | 7213 | c.-89G>C | upstream_gene_variant | 0.8 |
| gyrA | 7216 | c.-86G>T | upstream_gene_variant | 0.8 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 0.8 |
| gyrA | 7231 | c.-71C>A | upstream_gene_variant | 0.75 |
| gyrA | 7232 | c.-70_-68delCGCinsAGG | upstream_gene_variant | 0.75 |
| gyrA | 7243 | c.-59G>A | upstream_gene_variant | 0.67 |
| gyrA | 7246 | c.-56T>C | upstream_gene_variant | 1.0 |
| gyrA | 7252 | c.-50G>C | upstream_gene_variant | 1.0 |
| gyrA | 7256 | c.-46C>T | upstream_gene_variant | 1.0 |
| gyrA | 7340 | c.39C>T | synonymous_variant | 0.8 |
| gyrA | 7344 | p.Ile15Val | missense_variant | 0.89 |
| gyrA | 7349 | c.48A>G | synonymous_variant | 0.93 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 0.9 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7415 | c.114C>G | synonymous_variant | 0.98 |
| gyrA | 7422 | c.121C>T | synonymous_variant | 1.0 |
| gyrA | 7430 | c.129G>A | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | 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>A | synonymous_variant | 1.0 |
| gyrA | 7469 | c.168C>G | synonymous_variant | 1.0 |
| gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7490 | c.189C>G | synonymous_variant | 1.0 |
| gyrA | 7502 | c.201C>T | synonymous_variant | 1.0 |
| gyrA | 7514 | c.213C>A | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7556 | c.255C>T | synonymous_variant | 1.0 |
| gyrA | 7574 | c.273G>C | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7622 | c.321C>T | synonymous_variant | 1.0 |
| gyrA | 7625 | c.324G>C | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>T | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7700 | c.399G>A | synonymous_variant | 1.0 |
| gyrA | 7706 | c.405C>T | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7759 | p.Ile153Thr | missense_variant | 1.0 |
| gyrA | 7790 | c.489G>T | synonymous_variant | 1.0 |
| gyrA | 7793 | c.492G>A | synonymous_variant | 1.0 |
| gyrA | 7796 | c.495G>A | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7821 | c.520C>T | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>C | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7847 | c.546G>C | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7880 | c.579C>T | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
| gyrA | 7895 | c.594C>A | synonymous_variant | 1.0 |
| gyrA | 7898 | p.Asp199Glu | missense_variant | 1.0 |
| gyrA | 8054 | c.753T>C | synonymous_variant | 1.0 |
| gyrA | 8057 | c.756A>G | synonymous_variant | 1.0 |
| gyrA | 8071 | p.Val257Ala | missense_variant | 1.0 |
| gyrA | 8076 | p.Val259Ile | missense_variant | 1.0 |
| gyrA | 8084 | c.783G>A | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>A | synonymous_variant | 1.0 |
| gyrA | 8094 | p.Gly265Ser | missense_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8102 | c.801C>G | synonymous_variant | 1.0 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8120 | c.819G>A | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8190 | p.Ala297Ser | missense_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8199 | p.Ser300Ala | missense_variant | 1.0 |
| gyrA | 8237 | c.936A>G | synonymous_variant | 1.0 |
| gyrA | 8253 | p.Ile318Leu | missense_variant | 1.0 |
| gyrA | 8264 | c.963T>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 | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8372 | c.1071G>A | synonymous_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8378 | c.1077C>T | synonymous_variant | 1.0 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8408 | c.1107A>G | synonymous_variant | 1.0 |
| gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>A | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8489 | c.1188A>G | synonymous_variant | 0.97 |
| gyrA | 8501 | c.1200G>C | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 0.96 |
| gyrA | 8513 | c.1212C>G | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>G | synonymous_variant | 1.0 |
| gyrA | 8525 | c.1224C>T | synonymous_variant | 1.0 |
| gyrA | 8580 | p.Ile427Val | missense_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
| gyrA | 8627 | c.1326C>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 | 8648 | c.1347G>A | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8678 | c.1377G>A | synonymous_variant | 1.0 |
| gyrA | 8684 | c.1383G>A | synonymous_variant | 1.0 |
| gyrA | 8690 | c.1389C>T | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8705 | c.1404C>T | synonymous_variant | 1.0 |
| gyrA | 8706 | c.1405C>T | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8717 | c.1416C>G | synonymous_variant | 1.0 |
| gyrA | 8718 | p.Glu473Lys | missense_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8783 | c.1482G>C | synonymous_variant | 1.0 |
| gyrA | 8789 | c.1488C>T | synonymous_variant | 1.0 |
| gyrA | 8792 | c.1491G>C | synonymous_variant | 1.0 |
| gyrA | 8796 | p.Ile499Val | missense_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 0.93 |
| gyrA | 8813 | p.Asp504Glu | missense_variant | 0.94 |
| gyrA | 8822 | c.1521C>T | synonymous_variant | 0.96 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 0.97 |
| gyrA | 8836 | p.Ala512Val | missense_variant | 0.98 |
| gyrA | 8840 | c.1539C>G | synonymous_variant | 0.98 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 0.98 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 0.98 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 0.97 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 0.97 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 0.98 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 0.98 |
| gyrA | 8918 | c.1617C>G | synonymous_variant | 0.95 |
| gyrA | 8930 | c.1629C>G | synonymous_variant | 0.98 |
| gyrA | 8933 | c.1632G>C | synonymous_variant | 0.98 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 0.98 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 0.98 |
| gyrA | 8978 | c.1677C>T | 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 | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9056 | c.1755C>A | synonymous_variant | 1.0 |
| gyrA | 9059 | c.1758G>A | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9074 | c.1773G>A | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 9104 | c.1803C>G | synonymous_variant | 1.0 |
| gyrA | 9110 | c.1809G>A | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9122 | c.1821C>G | synonymous_variant | 1.0 |
| gyrA | 9128 | c.1827C>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9147 | p.Gly616Ser | missense_variant | 0.88 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 0.88 |
| gyrA | 9167 | c.1866C>T | synonymous_variant | 0.88 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 0.86 |
| gyrA | 9191 | c.1890G>T | synonymous_variant | 0.86 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 0.9 |
| gyrA | 9212 | c.1911G>C | synonymous_variant | 0.9 |
| gyrA | 9227 | c.1926C>G | synonymous_variant | 0.91 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 0.91 |
| gyrA | 9236 | c.1935G>A | synonymous_variant | 0.91 |
| gyrA | 9242 | c.1941A>G | synonymous_variant | 0.91 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9267 | p.Asn656Gly | missense_variant | 1.0 |
| gyrA | 9284 | c.1983T>G | synonymous_variant | 1.0 |
| gyrA | 9291 | c.1990C>T | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9320 | c.2019G>C | synonymous_variant | 1.0 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9345 | c.2044A>C | synonymous_variant | 1.0 |
| gyrA | 9362 | c.2061C>T | synonymous_variant | 1.0 |
| gyrA | 9365 | p.Glu688Asp | missense_variant | 1.0 |
| gyrA | 9369 | c.2068C>T | synonymous_variant | 1.0 |
| gyrA | 9374 | c.2073G>T | synonymous_variant | 1.0 |
| 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 | 9419 | c.2118T>C | synonymous_variant | 1.0 |
| gyrA | 9420 | p.Ile707Ala | missense_variant | 0.95 |
| gyrA | 9429 | p.Arg710Tyr | missense_variant | 1.0 |
| gyrA | 9449 | c.2148C>G | synonymous_variant | 1.0 |
| gyrA | 9452 | c.2151G>C | synonymous_variant | 1.0 |
| gyrA | 9455 | c.2154T>G | synonymous_variant | 1.0 |
| gyrA | 9464 | c.2163C>A | synonymous_variant | 1.0 |
| gyrA | 9476 | c.2175G>C | synonymous_variant | 1.0 |
| gyrA | 9485 | c.2184A>G | synonymous_variant | 1.0 |
| gyrA | 9488 | c.2187G>A | synonymous_variant | 1.0 |
| gyrA | 9497 | c.2196G>C | synonymous_variant | 1.0 |
| gyrA | 9611 | p.Asp770Glu | missense_variant | 1.0 |
| gyrA | 9617 | c.2316C>T | synonymous_variant | 1.0 |
| gyrA | 9621 | p.Leu774Val | missense_variant | 1.0 |
| gyrA | 9630 | p.Val777Ile | missense_variant | 1.0 |
| gyrA | 9635 | c.2334T>C | synonymous_variant | 1.0 |
| gyrA | 9641 | c.2340C>T | synonymous_variant | 1.0 |
| gyrA | 9644 | c.2343T>A | synonymous_variant | 1.0 |
| gyrA | 9656 | c.2355C>G | synonymous_variant | 1.0 |
| gyrA | 9659 | c.2358C>G | synonymous_variant | 1.0 |
| gyrA | 9665 | c.2364A>C | synonymous_variant | 1.0 |
| gyrA | 9668 | c.2367C>G | synonymous_variant | 1.0 |
| gyrA | 9683 | c.2382G>C | synonymous_variant | 1.0 |
| gyrA | 9686 | c.2385A>G | synonymous_variant | 1.0 |
| gyrA | 9695 | c.2394C>T | synonymous_variant | 1.0 |
| gyrA | 9701 | c.2400T>C | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9717 | c.2416C>T | synonymous_variant | 1.0 |
| gyrA | 9740 | c.2439G>A | synonymous_variant | 1.0 |
| gyrA | 9746 | c.2445C>T | synonymous_variant | 1.0 |
| gyrA | 9749 | c.2448G>A | synonymous_variant | 1.0 |
| fgd1 | 490830 | c.48A>G | synonymous_variant | 0.75 |
| fgd1 | 490836 | c.54C>G | synonymous_variant | 1.0 |
| fgd1 | 490842 | c.60C>T | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>G | synonymous_variant | 1.0 |
| fgd1 | 490854 | c.72C>G | synonymous_variant | 1.0 |
| fgd1 | 490866 | c.84A>G | synonymous_variant | 1.0 |
| fgd1 | 490869 | c.87C>G | synonymous_variant | 1.0 |
| fgd1 | 490872 | c.90C>T | synonymous_variant | 1.0 |
| fgd1 | 490875 | c.93C>G | synonymous_variant | 1.0 |
| fgd1 | 490887 | c.105G>C | synonymous_variant | 1.0 |
| fgd1 | 490890 | c.108C>T | synonymous_variant | 1.0 |
| fgd1 | 490899 | c.117C>T | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 0.89 |
| fgd1 | 490911 | c.129T>G | synonymous_variant | 0.94 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 0.94 |
| fgd1 | 490921 | p.Gln47Lys | missense_variant | 0.94 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 0.94 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 0.94 |
| fgd1 | 490962 | c.180T>C | synonymous_variant | 0.89 |
| fgd1 | 490971 | c.189A>G | synonymous_variant | 0.83 |
| fgd1 | 490974 | c.192T>C | synonymous_variant | 0.8 |
| fgd1 | 490978 | p.Asn66Glu | missense_variant | 0.8 |
| fgd1 | 490981 | c.199C>A | synonymous_variant | 0.8 |
| fgd1 | 490984 | p.Leu68Ile | missense_variant | 0.8 |
| fgd1 | 490987 | p.Leu69Val | missense_variant | 0.8 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 0.8 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 1.0 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 1.0 |
| fgd1 | 491016 | c.234C>A | synonymous_variant | 1.0 |
| fgd1 | 491022 | c.240C>G | synonymous_variant | 1.0 |
| fgd1 | 491025 | c.243C>T | synonymous_variant | 1.0 |
| fgd1 | 491091 | c.309T>G | synonymous_variant | 1.0 |
| fgd1 | 491097 | c.315G>T | synonymous_variant | 1.0 |
| fgd1 | 491106 | c.324T>G | synonymous_variant | 1.0 |
| fgd1 | 491112 | c.330G>T | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491133 | c.351A>C | synonymous_variant | 1.0 |
| fgd1 | 491142 | c.360C>T | synonymous_variant | 1.0 |
| fgd1 | 491145 | c.363C>G | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491196 | c.414A>G | synonymous_variant | 1.0 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 1.0 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 1.0 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 1.0 |
| fgd1 | 491217 | c.435T>C | synonymous_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 1.0 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 1.0 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 1.0 |
| fgd1 | 491310 | c.528C>G | synonymous_variant | 1.0 |
| fgd1 | 491313 | c.531C>G | synonymous_variant | 1.0 |
| fgd1 | 491322 | c.540G>A | synonymous_variant | 1.0 |
| fgd1 | 491331 | c.549G>A | synonymous_variant | 1.0 |
| fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
| fgd1 | 491340 | c.558C>G | synonymous_variant | 1.0 |
| fgd1 | 491343 | c.561C>G | synonymous_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491382 | c.600G>A | synonymous_variant | 1.0 |
| fgd1 | 491388 | c.606C>G | synonymous_variant | 1.0 |
| fgd1 | 491397 | c.615G>A | synonymous_variant | 1.0 |
| fgd1 | 491409 | c.627G>C | synonymous_variant | 1.0 |
| fgd1 | 491415 | c.633A>G | synonymous_variant | 1.0 |
| fgd1 | 491447 | p.Val222Ala | missense_variant | 1.0 |
| fgd1 | 491453 | p.Gly224Asp | missense_variant | 1.0 |
| fgd1 | 491472 | c.690A>G | synonymous_variant | 1.0 |
| fgd1 | 491493 | c.711C>T | synonymous_variant | 1.0 |
| fgd1 | 491502 | c.720G>A | synonymous_variant | 1.0 |
| fgd1 | 491508 | c.726A>C | synonymous_variant | 1.0 |
| fgd1 | 491509 | p.Leu243Arg | missense_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.96 |
| fgd1 | 491520 | c.738C>T | synonymous_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 | 491574 | c.792C>T | synonymous_variant | 1.0 |
| fgd1 | 491589 | c.807G>A | synonymous_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>C | synonymous_variant | 1.0 |
| fgd1 | 491637 | c.855C>T | synonymous_variant | 1.0 |
| fgd1 | 491640 | c.858G>C | synonymous_variant | 1.0 |
| fgd1 | 491658 | c.876A>G | synonymous_variant | 1.0 |
| fgd1 | 491661 | c.879C>T | synonymous_variant | 1.0 |
| fgd1 | 491670 | c.888G>A | synonymous_variant | 1.0 |
| fgd1 | 491673 | c.891A>C | synonymous_variant | 1.0 |
| fgd1 | 491676 | c.894T>C | synonymous_variant | 1.0 |
| fgd1 | 491679 | c.897A>G | synonymous_variant | 1.0 |
| fgd1 | 491685 | c.903G>C | synonymous_variant | 1.0 |
| fgd1 | 491688 | c.906A>G | synonymous_variant | 1.0 |
| fgd1 | 491695 | p.Leu305Phe | missense_variant | 1.0 |
| fgd1 | 491703 | c.921C>T | synonymous_variant | 1.0 |
| fgd1 | 491709 | c.927A>C | synonymous_variant | 1.0 |
| mshA | 575530 | c.183C>T | synonymous_variant | 1.0 |
| mshA | 575532 | p.Thr62Ile | missense_variant | 1.0 |
| mshA | 575536 | c.189T>G | synonymous_variant | 0.8 |
| mshA | 575548 | c.201C>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 | 575576 | c.229C>T | synonymous_variant | 1.0 |
| mshA | 575581 | c.234C>T | synonymous_variant | 1.0 |
| mshA | 575587 | c.240C>T | synonymous_variant | 1.0 |
| mshA | 575593 | c.246G>C | synonymous_variant | 0.78 |
| mshA | 575602 | p.Glu85Asp | missense_variant | 1.0 |
| mshA | 575629 | c.282A>G | synonymous_variant | 1.0 |
| mshA | 575632 | c.285G>C | synonymous_variant | 0.92 |
| mshA | 575633 | p.Ala96Thr | missense_variant | 0.92 |
| mshA | 575641 | c.294A>G | synonymous_variant | 0.93 |
| mshA | 575645 | p.Val100Ile | missense_variant | 0.93 |
| mshA | 575659 | c.312A>G | synonymous_variant | 0.95 |
| mshA | 575689 | c.342G>C | synonymous_variant | 0.92 |
| mshA | 575695 | c.348C>G | synonymous_variant | 0.96 |
| mshA | 575704 | c.357T>C | synonymous_variant | 0.95 |
| mshA | 575705 | c.358T>C | synonymous_variant | 0.95 |
| mshA | 575713 | c.366G>A | synonymous_variant | 0.95 |
| mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575740 | c.393G>C | synonymous_variant | 1.0 |
| mshA | 575770 | c.423G>T | synonymous_variant | 0.97 |
| mshA | 575772 | p.Val142Ala | missense_variant | 0.97 |
| mshA | 575782 | c.435G>C | synonymous_variant | 0.97 |
| mshA | 575785 | c.438T>C | synonymous_variant | 0.97 |
| mshA | 575812 | c.465C>T | synonymous_variant | 0.97 |
| mshA | 575816 | c.469C>T | synonymous_variant | 0.97 |
| mshA | 575821 | c.474G>C | synonymous_variant | 0.97 |
| mshA | 575824 | c.477T>G | synonymous_variant | 0.94 |
| mshA | 575842 | c.495G>C | synonymous_variant | 0.96 |
| mshA | 575845 | c.498C>G | synonymous_variant | 0.95 |
| mshA | 575864 | c.517T>C | synonymous_variant | 0.95 |
| mshA | 575878 | c.531A>G | synonymous_variant | 1.0 |
| mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
| mshA | 575908 | c.561A>G | synonymous_variant | 1.0 |
| mshA | 575920 | c.573C>T | synonymous_variant | 1.0 |
| mshA | 575924 | p.Gly193Thr | missense_variant | 1.0 |
| mshA | 575932 | c.585G>A | synonymous_variant | 1.0 |
| mshA | 575944 | c.597T>G | synonymous_variant | 1.0 |
| mshA | 575953 | c.606G>C | synonymous_variant | 1.0 |
| mshA | 575965 | c.618C>G | synonymous_variant | 1.0 |
| mshA | 575980 | c.633T>C | synonymous_variant | 1.0 |
| mshA | 576001 | p.Asp218Glu | missense_variant | 1.0 |
| ccsA | 620173 | p.Val95Ile | missense_variant | 0.8 |
| ccsA | 620187 | c.297C>T | synonymous_variant | 0.8 |
| ccsA | 620197 | p.Gln103Ala | missense_variant | 0.8 |
| ccsA | 620202 | c.312G>C | synonymous_variant | 0.83 |
| ccsA | 620208 | c.318G>C | synonymous_variant | 0.93 |
| ccsA | 620247 | p.Leu119Phe | missense_variant | 0.97 |
| ccsA | 620249 | p.Ser120Cys | missense_variant | 0.97 |
| ccsA | 620256 | c.366C>G | synonymous_variant | 0.97 |
| ccsA | 620257 | p.Ile123Val | missense_variant | 0.97 |
| ccsA | 620269 | p.Val127Ile | missense_variant | 0.96 |
| ccsA | 620275 | c.385_387delCTGinsTTA | synonymous_variant | 0.96 |
| ccsA | 620283 | c.393T>A | synonymous_variant | 0.96 |
| ccsA | 620284 | p.Ala132Pro | missense_variant | 0.96 |
| ccsA | 620288 | p.Arg133Gln | missense_variant | 0.96 |
| ccsA | 620307 | c.417C>T | synonymous_variant | 0.96 |
| ccsA | 620316 | c.426G>C | synonymous_variant | 0.86 |
| ccsA | 620317 | p.Val143Leu | missense_variant | 0.83 |
| ccsA | 620325 | c.435G>C | synonymous_variant | 0.83 |
| ccsA | 620331 | c.441C>T | synonymous_variant | 1.0 |
| ccsA | 620332 | c.442C>T | synonymous_variant | 1.0 |
| ccsA | 620337 | c.447C>G | synonymous_variant | 1.0 |
| ccsA | 620340 | c.450C>T | synonymous_variant | 1.0 |
| ccsA | 620349 | c.459A>G | synonymous_variant | 1.0 |
| ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
| ccsA | 620373 | c.483C>G | synonymous_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620412 | c.522T>C | synonymous_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620418 | c.528G>C | synonymous_variant | 1.0 |
| ccsA | 620445 | c.555A>G | synonymous_variant | 1.0 |
| ccsA | 620448 | c.558C>T | synonymous_variant | 1.0 |
| ccsA | 620457 | c.567C>G | synonymous_variant | 1.0 |
| ccsA | 620460 | c.570T>C | synonymous_variant | 1.0 |
| ccsA | 620463 | c.573C>G | synonymous_variant | 1.0 |
| ccsA | 620481 | c.591T>G | synonymous_variant | 1.0 |
| ccsA | 620482 | p.Val198Leu | missense_variant | 1.0 |
| ccsA | 620487 | c.597C>G | synonymous_variant | 1.0 |
| ccsA | 620490 | c.600A>G | synonymous_variant | 1.0 |
| ccsA | 620502 | c.612T>C | synonymous_variant | 1.0 |
| ccsA | 620586 | c.696C>G | synonymous_variant | 1.0 |
| ccsA | 620597 | p.Ala236Gly | missense_variant | 1.0 |
| ccsA | 620604 | c.714C>G | synonymous_variant | 1.0 |
| ccsA | 620607 | c.717T>C | synonymous_variant | 1.0 |
| ccsA | 620613 | c.723C>T | synonymous_variant | 1.0 |
| ccsA | 620631 | c.741T>C | synonymous_variant | 1.0 |
| ccsA | 620634 | c.744C>G | synonymous_variant | 1.0 |
| ccsA | 620647 | p.Glu253Gln | missense_variant | 1.0 |
| ccsA | 620652 | c.762C>A | synonymous_variant | 1.0 |
| ccsA | 620658 | c.768C>T | synonymous_variant | 1.0 |
| ccsA | 620661 | c.771C>G | synonymous_variant | 1.0 |
| ccsA | 620670 | c.780C>A | synonymous_variant | 1.0 |
| ccsA | 620676 | c.786C>T | synonymous_variant | 1.0 |
| ccsA | 620692 | p.Ser268Ala | missense_variant | 1.0 |
| ccsA | 620698 | p.Val270Ile | missense_variant | 1.0 |
| ccsA | 620707 | p.Val273Met | missense_variant | 1.0 |
| ccsA | 620715 | c.825C>T | synonymous_variant | 1.0 |
| ccsA | 620718 | c.828G>C | synonymous_variant | 1.0 |
| ccsA | 620721 | c.831G>C | synonymous_variant | 1.0 |
| ccsA | 620730 | c.840C>T | synonymous_variant | 1.0 |
| ccsA | 620733 | c.843G>C | synonymous_variant | 1.0 |
| ccsA | 620734 | c.844C>A | synonymous_variant | 1.0 |
| ccsA | 620742 | c.852G>C | synonymous_variant | 1.0 |
| ccsA | 620748 | c.858T>A | synonymous_variant | 1.0 |
| ccsA | 620758 | c.868_870delCGCinsAGA | synonymous_variant | 1.0 |
| ccsA | 620778 | c.888T>C | synonymous_variant | 1.0 |
| ccsA | 620780 | p.Val297Ala | missense_variant | 1.0 |
| ccsA | 620787 | c.897C>A | synonymous_variant | 1.0 |
| ccsA | 620796 | c.906C>A | synonymous_variant | 1.0 |
| ccsA | 620808 | c.918T>C | synonymous_variant | 1.0 |
| ccsA | 620832 | c.942C>T | synonymous_variant | 1.0 |
| ccsA | 620835 | c.945C>G | synonymous_variant | 1.0 |
| ccsA | 620844 | c.954C>T | synonymous_variant | 1.0 |
| ccsA | 620847 | c.957G>A | synonymous_variant | 1.0 |
| ccsA | 620853 | c.963G>C | synonymous_variant | 1.0 |
| ccsA | 620856 | c.966C>T | synonymous_variant | 1.0 |
| ccsA | 620864 | c.974G>A | splice_region_variant&stop_retained_variant | 1.0 |
| rpoB | 759616 | c.-191C>T | upstream_gene_variant | 1.0 |
| rpoB | 759621 | c.-186C>T | upstream_gene_variant | 1.0 |
| rpoB | 759643 | c.-164T>C | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 759671 | c.-136G>C | upstream_gene_variant | 1.0 |
| rpoB | 759672 | c.-135G>A | upstream_gene_variant | 1.0 |
| rpoB | 759674 | c.-133T>C | upstream_gene_variant | 1.0 |
| rpoB | 759678 | c.-129T>C | upstream_gene_variant | 1.0 |
| rpoB | 759711 | c.-96G>A | upstream_gene_variant | 1.0 |
| rpoB | 759715 | c.-91delA | upstream_gene_variant | 1.0 |
| rpoB | 759725 | c.-82A>C | upstream_gene_variant | 1.0 |
| rpoB | 759727 | c.-80A>G | upstream_gene_variant | 1.0 |
| rpoB | 759732 | c.-75C>A | upstream_gene_variant | 1.0 |
| rpoB | 759911 | c.105C>T | synonymous_variant | 1.0 |
| rpoB | 759914 | c.108T>C | synonymous_variant | 1.0 |
| rpoB | 759923 | c.117C>T | synonymous_variant | 1.0 |
| rpoB | 759929 | c.123A>G | synonymous_variant | 1.0 |
| rpoB | 759932 | c.126T>C | synonymous_variant | 1.0 |
| rpoB | 759941 | c.135G>C | synonymous_variant | 1.0 |
| rpoB | 759944 | c.138A>T | synonymous_variant | 1.0 |
| rpoB | 759947 | c.141C>G | synonymous_variant | 1.0 |
| rpoB | 759950 | c.144T>G | synonymous_variant | 1.0 |
| rpoB | 759956 | c.150C>G | synonymous_variant | 1.0 |
| rpoB | 759965 | c.159T>C | synonymous_variant | 1.0 |
| rpoB | 759987 | p.Ser61Ala | missense_variant | 1.0 |
| rpoB | 760040 | c.234T>C | synonymous_variant | 1.0 |
| rpoB | 760059 | p.Tyr85Asp | missense_variant | 1.0 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 1.0 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760106 | c.300G>C | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>A | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>G | synonymous_variant | 0.98 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760139 | c.333A>C | synonymous_variant | 1.0 |
| rpoB | 760142 | c.336C>T | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>G | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| 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 | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760388 | c.582C>T | synonymous_variant | 1.0 |
| rpoB | 760389 | c.583_585delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760418 | c.612G>T | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760445 | c.639C>G | synonymous_variant | 1.0 |
| rpoB | 760451 | c.645C>G | synonymous_variant | 1.0 |
| rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760490 | c.684C>G | synonymous_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760576 | p.Glu257Gly | missense_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 | 1.0 |
| rpoB | 760643 | c.837G>A | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760664 | c.858G>A | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760710 | c.904C>T | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>G | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760745 | c.939G>A | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760796 | c.990A>G | synonymous_variant | 1.0 |
| rpoB | 760802 | c.996C>G | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760845 | p.Thr347Ala | missense_variant | 1.0 |
| rpoB | 760859 | c.1053T>C | synonymous_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>T | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
| rpoB | 761096 | c.1290G>C | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>G | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761183 | c.1377T>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>G | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>A | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761217 | p.Pro471Ser | missense_variant | 1.0 |
| rpoB | 761222 | c.1416G>C | synonymous_variant | 1.0 |
| rpoB | 761240 | c.1434C>T | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>G | synonymous_variant | 1.0 |
| rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
| rpoB | 761346 | p.Val514Arg | missense_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761374 | p.Val523Glu | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761411 | c.1605G>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.Ala544Asp | missense_variant | 1.0 |
| rpoB | 761444 | c.1638T>C | synonymous_variant | 1.0 |
| rpoB | 761447 | c.1641C>G | synonymous_variant | 1.0 |
| rpoB | 761451 | p.Val549Thr | missense_variant | 1.0 |
| rpoB | 761462 | c.1656C>T | synonymous_variant | 1.0 |
| rpoB | 761465 | c.1659G>C | synonymous_variant | 1.0 |
| rpoB | 761471 | c.1665C>G | synonymous_variant | 1.0 |
| rpoB | 761483 | c.1677G>C | synonymous_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761502 | p.Pro566Ser | missense_variant | 1.0 |
| rpoB | 761510 | c.1704T>G | synonymous_variant | 1.0 |
| rpoB | 761528 | c.1722C>T | synonymous_variant | 1.0 |
| rpoB | 761531 | c.1725C>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761549 | c.1743G>T | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | 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>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| 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 | 761655 | p.Ala617Arg | missense_variant | 0.97 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>T | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
| rpoB | 761724 | p.Glu640Lys | missense_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>G | synonymous_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761819 | c.2013G>C | synonymous_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761847 | p.Cys681Arg | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>C | synonymous_variant | 1.0 |
| rpoB | 761870 | p.Asp688Glu | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761882 | c.2076C>G | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 0.97 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761916 | p.Asp704Gln | missense_variant | 1.0 |
| rpoB | 761921 | c.2115C>T | synonymous_variant | 1.0 |
| rpoB | 761951 | c.2145G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762024 | p.Val740Ile | missense_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 | 762078 | c.2272C>T | 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 | 0.98 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 0.98 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 0.98 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 0.98 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 0.96 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 0.96 |
| rpoB | 762197 | c.2391C>T | synonymous_variant | 0.96 |
| rpoB | 762233 | c.2427G>T | synonymous_variant | 0.98 |
| rpoB | 762254 | c.2448T>C | 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>A | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762323 | c.2517C>A | 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 | 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 | 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 | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762521 | c.-849C>T | 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 | 762545 | c.-825C>G | upstream_gene_variant | 1.0 |
| rpoC | 762548 | c.-822C>T | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762554 | c.-816G>T | upstream_gene_variant | 0.97 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 1.0 |
| rpoC | 762587 | c.-783G>A | upstream_gene_variant | 1.0 |
| rpoC | 762596 | c.-774G>C | upstream_gene_variant | 1.0 |
| rpoC | 762599 | c.-771T>C | upstream_gene_variant | 1.0 |
| rpoC | 762605 | c.-765T>C | upstream_gene_variant | 1.0 |
| rpoC | 762608 | c.-762C>G | upstream_gene_variant | 1.0 |
| rpoB | 762624 | p.Val940Ile | missense_variant | 1.0 |
| rpoB | 762630 | p.Ala942Thr | missense_variant | 1.0 |
| rpoC | 762641 | c.-729G>C | upstream_gene_variant | 1.0 |
| rpoC | 762644 | c.-726T>G | upstream_gene_variant | 1.0 |
| rpoC | 762701 | c.-669T>C | upstream_gene_variant | 1.0 |
| rpoC | 762707 | c.-663G>C | upstream_gene_variant | 1.0 |
| rpoC | 762731 | c.-639G>A | upstream_gene_variant | 1.0 |
| rpoC | 762737 | c.-633C>G | upstream_gene_variant | 1.0 |
| rpoC | 762749 | c.-621C>T | upstream_gene_variant | 1.0 |
| rpoC | 762753 | c.-617T>C | upstream_gene_variant | 1.0 |
| rpoB | 762760 | p.Cys985Ser | missense_variant | 1.0 |
| rpoC | 762770 | c.-600C>T | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoC | 762785 | c.-585C>T | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762815 | p.Met1003Ile | missense_variant | 1.0 |
| rpoB | 762820 | p.Phe1005Tyr | missense_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>T | 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 |
| rpoB | 762861 | p.Val1019Thr | missense_variant | 1.0 |
| rpoC | 762890 | c.-480C>T | upstream_gene_variant | 1.0 |
| rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>C | 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 | 763115 | c.-255T>G | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>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 | 763193 | c.-177C>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 | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoB | 763227 | p.Leu1141Met | missense_variant | 1.0 |
| rpoB | 763235 | p.Glu1143Asp | missense_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoB | 763241 | p.Glu1145Asp | missense_variant | 1.0 |
| rpoC | 763259 | c.-111G>C | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
| rpoC | 763284 | c.-86C>T | upstream_gene_variant | 1.0 |
| rpoC | 763369 | c.-1C>T | upstream_gene_variant | 1.0 |
| rpoC | 763373 | c.4_6delCTCinsTTA | synonymous_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763409 | c.40_42delCTTinsTTG | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763420 | c.51G>C | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61A>C | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763441 | c.72C>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763453 | c.84C>G | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763483 | c.114G>A | synonymous_variant | 1.0 |
| rpoC | 763484 | c.115_117delCTTinsTTG | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763621 | c.252C>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 | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>T | synonymous_variant | 0.98 |
| rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>C | 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>G | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763771 | c.402C>T | synonymous_variant | 1.0 |
| rpoC | 763780 | c.411C>G | synonymous_variant | 1.0 |
| rpoC | 763783 | c.414G>C | synonymous_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 0.97 |
| 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.Ala156Thr | missense_variant | 1.0 |
| rpoC | 763852 | c.483C>G | synonymous_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>C | synonymous_variant | 1.0 |
| rpoC | 763885 | c.516C>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>T | synonymous_variant | 0.95 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763903 | c.534G>A | synonymous_variant | 1.0 |
| rpoC | 763918 | c.549G>A | synonymous_variant | 1.0 |
| rpoC | 763936 | c.567C>G | synonymous_variant | 1.0 |
| rpoC | 763939 | c.570G>A | synonymous_variant | 1.0 |
| rpoC | 763969 | c.600C>T | synonymous_variant | 1.0 |
| rpoC | 763978 | c.609C>G | synonymous_variant | 1.0 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764011 | c.642T>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655T>C | synonymous_variant | 1.0 |
| rpoC | 764040 | p.Ser224Asn | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764119 | c.750G>A | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 0.99 |
| rpoC | 764161 | c.792G>C | synonymous_variant | 1.0 |
| rpoC | 764167 | c.798G>A | synonymous_variant | 1.0 |
| rpoC | 764169 | p.Asn267Ser | missense_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764194 | p.Glu275Asp | missense_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ala | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>T | synonymous_variant | 1.0 |
| rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
| rpoC | 764227 | c.858G>A | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764284 | c.915G>C | synonymous_variant | 1.0 |
| rpoC | 764285 | p.Gly306Thr | missense_variant | 1.0 |
| rpoC | 764317 | c.948C>G | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>G | synonymous_variant | 1.0 |
| rpoC | 764338 | c.969G>A | synonymous_variant | 1.0 |
| rpoC | 764344 | c.975C>T | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764392 | c.1023C>T | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764494 | c.1125G>A | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 0.9 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764551 | c.1182G>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>C | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764851 | c.1482C>T | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>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>G | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764983 | c.1614T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>C | 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 | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>C | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>C | synonymous_variant | 1.0 |
| rpoC | 765085 | c.1716T>C | synonymous_variant | 1.0 |
| rpoC | 765122 | c.1753C>T | synonymous_variant | 1.0 |
| rpoC | 765142 | c.1773G>A | synonymous_variant | 1.0 |
| rpoC | 765145 | c.1776C>T | synonymous_variant | 1.0 |
| rpoC | 765151 | c.1782G>C | synonymous_variant | 1.0 |
| rpoC | 765334 | c.1965C>T | synonymous_variant | 1.0 |
| rpoC | 765343 | c.1974G>A | synonymous_variant | 1.0 |
| rpoC | 765346 | c.1977C>T | synonymous_variant | 1.0 |
| rpoC | 765350 | p.Ala661Ser | missense_variant | 1.0 |
| rpoC | 765376 | c.2007C>T | 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 | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Ser | missense_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | synonymous_variant | 1.0 |
| rpoC | 765472 | c.2103C>T | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>G | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765523 | c.2154C>T | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 1.0 |
| rpoC | 765547 | c.2178C>G | synonymous_variant | 1.0 |
| rpoC | 765548 | c.2179_2181delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 1.0 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 1.0 |
| rpoC | 765559 | c.2190G>C | synonymous_variant | 1.0 |
| rpoC | 765578 | c.2209C>T | synonymous_variant | 1.0 |
| rpoC | 765584 | p.Pro739Ala | missense_variant | 1.0 |
| rpoC | 765590 | p.Arg741Gly | missense_variant | 1.0 |
| rpoC | 765596 | p.Lys743Gln | missense_variant | 1.0 |
| rpoC | 765611 | p.His748Ala | missense_variant | 1.0 |
| rpoC | 765619 | c.2250G>A | synonymous_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765658 | c.2289C>T | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765727 | c.2358T>C | synonymous_variant | 1.0 |
| rpoC | 765728 | p.Gln787Glu | missense_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>C | synonymous_variant | 1.0 |
| rpoC | 765740 | p.Glu791Lys | missense_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765787 | c.2418C>T | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
| rpoC | 765823 | c.2454C>G | synonymous_variant | 0.98 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 0.98 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 0.98 |
| rpoC | 765868 | c.2499G>A | synonymous_variant | 0.98 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 0.98 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 0.98 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 0.97 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 0.97 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 0.97 |
| rpoC | 765908 | c.2539C>T | synonymous_variant | 0.97 |
| rpoC | 765937 | c.2568T>G | synonymous_variant | 0.98 |
| rpoC | 765940 | c.2571A>G | synonymous_variant | 0.98 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 0.98 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 0.98 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 0.97 |
| rpoC | 765985 | c.2616C>T | synonymous_variant | 1.0 |
| rpoC | 765991 | c.2622C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766034 | p.His889Gly | missense_variant | 1.0 |
| rpoC | 766043 | p.Gln892Gly | missense_variant | 1.0 |
| rpoC | 766061 | p.Val898Thr | missense_variant | 1.0 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 1.0 |
| rpoC | 766109 | p.Pro914Ala | missense_variant | 1.0 |
| rpoC | 766113 | p.Tyr915Phe | missense_variant | 1.0 |
| rpoC | 766126 | c.2757G>C | synonymous_variant | 1.0 |
| rpoC | 766135 | c.2766G>C | synonymous_variant | 1.0 |
| rpoC | 766138 | c.2769G>C | synonymous_variant | 1.0 |
| rpoC | 766141 | c.2772C>T | synonymous_variant | 1.0 |
| rpoC | 766142 | c.2773C>T | synonymous_variant | 1.0 |
| rpoC | 766147 | c.2778C>T | synonymous_variant | 1.0 |
| rpoC | 766148 | p.Thr927Ala | missense_variant | 1.0 |
| rpoC | 766156 | c.2787G>C | synonymous_variant | 1.0 |
| rpoC | 766243 | c.2874C>G | synonymous_variant | 1.0 |
| rpoC | 766249 | c.2880C>G | synonymous_variant | 1.0 |
| rpoC | 766270 | c.2901G>C | synonymous_variant | 1.0 |
| rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766288 | c.2919C>G | synonymous_variant | 1.0 |
| rpoC | 766291 | c.2922G>C | synonymous_variant | 1.0 |
| rpoC | 766298 | p.Thr977Val | missense_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766357 | c.2988C>T | synonymous_variant | 0.98 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 0.98 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpoC | 766471 | c.3102G>C | synonymous_variant | 1.0 |
| rpoC | 766480 | c.3111C>T | synonymous_variant | 1.0 |
| rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766495 | c.3126C>T | synonymous_variant | 1.0 |
| rpoC | 766510 | c.3141C>A | synonymous_variant | 1.0 |
| rpoC | 766519 | c.3150C>A | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766546 | p.Glu1059Asp | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766570 | c.3201T>C | synonymous_variant | 1.0 |
| rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766618 | c.3249G>C | synonymous_variant | 1.0 |
| rpoC | 766624 | c.3255G>C | synonymous_variant | 1.0 |
| rpoC | 766642 | c.3273C>T | synonymous_variant | 1.0 |
| rpoC | 766645 | c.3276A>G | synonymous_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766652 | p.Ser1095Thr | missense_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
| rpoC | 766667 | p.Ser1100Ala | missense_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766714 | c.3345G>C | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>T | synonymous_variant | 1.0 |
| rpoC | 766756 | c.3387G>A | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766846 | c.3477C>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>T | synonymous_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 | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766918 | c.3549C>T | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>C | synonymous_variant | 1.0 |
| rpoC | 766942 | c.3573C>T | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766960 | c.3591C>T | synonymous_variant | 0.97 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 0.97 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 0.97 |
| rpoC | 766978 | c.3609C>T | synonymous_variant | 0.97 |
| rpoC | 766981 | c.3612T>C | synonymous_variant | 0.94 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 0.96 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 0.96 |
| rpoC | 767023 | c.3654C>T | synonymous_variant | 0.97 |
| rpoC | 767032 | c.3663G>C | synonymous_variant | 0.97 |
| rpoC | 767035 | c.3666G>C | synonymous_variant | 0.97 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 0.99 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 0.99 |
| rpoC | 767066 | c.3697C>T | synonymous_variant | 0.99 |
| rpoC | 767071 | c.3702C>G | synonymous_variant | 0.99 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>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 | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 0.96 |
| 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 |
| mmpL5 | 776678 | c.1801_1803delCGGinsAGA | synonymous_variant | 1.0 |
| mmpL5 | 776695 | p.Val596Ile | missense_variant | 1.0 |
| mmpL5 | 776696 | c.1785G>C | synonymous_variant | 1.0 |
| mmpL5 | 776699 | c.1782C>T | synonymous_variant | 1.0 |
| mmpL5 | 776702 | c.1779C>T | synonymous_variant | 1.0 |
| mmpL5 | 776705 | c.1776C>T | synonymous_variant | 1.0 |
| mmpL5 | 776714 | c.1767G>A | synonymous_variant | 1.0 |
| mmpL5 | 776744 | c.1735_1737delCGCinsAGA | synonymous_variant | 1.0 |
| mmpL5 | 776747 | p.Phe578Trp | missense_variant | 1.0 |
| mmpL5 | 776756 | p.Asp575Glu | missense_variant | 1.0 |
| mmpL5 | 776774 | c.1707C>T | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781592 | c.33T>G | synonymous_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Gly | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781679 | c.120C>G | 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 | 781724 | c.165G>C | 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 | 781742 | c.183C>T | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>T | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781835 | c.276T>C | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781889 | c.330C>T | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781913 | c.354C>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800630 | c.-179G>C | upstream_gene_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800642 | c.-167C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800666 | c.-143C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | 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 | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800726 | c.-83G>A | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>G | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| rplC | 800765 | c.-44G>C | upstream_gene_variant | 1.0 |
| rplC | 800814 | c.6A>G | synonymous_variant | 1.0 |
| rplC | 800815 | c.7C>A | synonymous_variant | 1.0 |
| rplC | 800829 | c.21C>G | synonymous_variant | 1.0 |
| rplC | 800832 | c.24T>C | synonymous_variant | 1.0 |
| rplC | 800841 | c.33G>T | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 0.88 |
| rplC | 800862 | c.54C>T | synonymous_variant | 0.86 |
| rplC | 800865 | c.57A>G | synonymous_variant | 0.8 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 0.8 |
| rplC | 800872 | c.64_66delAGAinsCGG | synonymous_variant | 0.8 |
| rplC | 800877 | c.69A>T | synonymous_variant | 0.8 |
| rplC | 800880 | c.72A>C | synonymous_variant | 0.8 |
| rplC | 800889 | c.81C>G | synonymous_variant | 0.92 |
| rplC | 800907 | c.99C>G | synonymous_variant | 0.94 |
| rplC | 800916 | c.108A>G | synonymous_variant | 0.94 |
| rplC | 800922 | c.114C>A | synonymous_variant | 0.94 |
| rplC | 800934 | c.126C>G | synonymous_variant | 0.95 |
| rplC | 800937 | c.129A>G | synonymous_variant | 0.95 |
| rplC | 800946 | c.138T>C | synonymous_variant | 1.0 |
| rplC | 800949 | c.141T>C | synonymous_variant | 1.0 |
| rplC | 800962 | c.154C>T | synonymous_variant | 1.0 |
| rplC | 800967 | c.159C>T | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800982 | c.174C>T | synonymous_variant | 1.0 |
| rplC | 800985 | c.177A>C | synonymous_variant | 1.0 |
| rplC | 801008 | p.Thr67Asn | missense_variant | 1.0 |
| rplC | 801018 | c.210C>T | synonymous_variant | 0.91 |
| rplC | 801020 | p.Thr71Ile | missense_variant | 0.91 |
| rplC | 801027 | c.219C>A | synonymous_variant | 0.89 |
| rplC | 801030 | c.222C>T | synonymous_variant | 0.86 |
| rplC | 801039 | c.231A>G | synonymous_variant | 0.75 |
| rplC | 801042 | c.234C>T | synonymous_variant | 0.67 |
| rplC | 801117 | c.309G>C | synonymous_variant | 1.0 |
| rplC | 801127 | p.Ala107Thr | missense_variant | 1.0 |
| rplC | 801132 | c.324T>C | synonymous_variant | 1.0 |
| rplC | 801135 | c.327C>A | synonymous_variant | 1.0 |
| rplC | 801141 | c.333C>T | synonymous_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801153 | c.345G>C | synonymous_variant | 1.0 |
| rplC | 801156 | c.348T>C | synonymous_variant | 1.0 |
| rplC | 801162 | c.354C>G | synonymous_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801183 | c.375C>A | synonymous_variant | 1.0 |
| rplC | 801201 | c.393C>T | synonymous_variant | 1.0 |
| rplC | 801210 | c.402T>G | synonymous_variant | 1.0 |
| rplC | 801222 | c.414T>C | synonymous_variant | 1.0 |
| rplC | 801228 | c.420T>C | synonymous_variant | 1.0 |
| rplC | 801231 | c.423C>T | synonymous_variant | 1.0 |
| rplC | 801240 | c.432G>A | synonymous_variant | 1.0 |
| rplC | 801243 | c.435C>T | synonymous_variant | 1.0 |
| rplC | 801246 | c.438C>T | synonymous_variant | 1.0 |
| rplC | 801267 | c.459A>T | synonymous_variant | 0.97 |
| rplC | 801270 | c.462T>C | synonymous_variant | 1.0 |
| rplC | 801273 | c.465C>G | synonymous_variant | 1.0 |
| rplC | 801276 | c.468G>A | synonymous_variant | 1.0 |
| rplC | 801285 | c.477G>A | synonymous_variant | 0.97 |
| rplC | 801300 | c.492C>G | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| rplC | 801321 | c.513C>T | synonymous_variant | 1.0 |
| rplC | 801324 | c.516T>C | synonymous_variant | 1.0 |
| rplC | 801330 | c.522G>C | synonymous_variant | 1.0 |
| rplC | 801337 | p.Val177Thr | missense_variant | 1.0 |
| rplC | 801341 | p.Leu178Gln | missense_variant | 1.0 |
| rplC | 801357 | c.549T>C | synonymous_variant | 1.0 |
| rplC | 801382 | c.574C>T | synonymous_variant | 1.0 |
| rplC | 801399 | c.591G>C | synonymous_variant | 1.0 |
| rplC | 801400 | p.Val198Ile | missense_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801413 | p.Thr202Asn | missense_variant | 1.0 |
| rplC | 801417 | c.609T>C | synonymous_variant | 1.0 |
| rplC | 801420 | c.612A>G | synonymous_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 1.0 |
| fbiC | 1303441 | c.511T>C | synonymous_variant | 1.0 |
| fbiC | 1303449 | c.519C>T | synonymous_variant | 1.0 |
| fbiC | 1303455 | c.525C>G | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303474 | c.544C>T | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303488 | c.558G>A | synonymous_variant | 1.0 |
| fbiC | 1303500 | c.570C>T | synonymous_variant | 1.0 |
| fbiC | 1303501 | c.571C>T | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303531 | p.Met201Leu | missense_variant | 1.0 |
| fbiC | 1303537 | c.607C>A | synonymous_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303557 | c.627G>C | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>G | synonymous_variant | 1.0 |
| fbiC | 1303611 | c.681G>T | synonymous_variant | 1.0 |
| fbiC | 1303632 | c.702T>C | synonymous_variant | 1.0 |
| fbiC | 1303638 | c.708A>G | synonymous_variant | 1.0 |
| fbiC | 1303641 | c.711C>T | synonymous_variant | 1.0 |
| fbiC | 1303659 | c.729T>G | synonymous_variant | 1.0 |
| fbiC | 1303660 | p.Val244Ser | missense_variant | 1.0 |
| fbiC | 1303663 | c.733C>T | synonymous_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303681 | c.751T>C | synonymous_variant | 0.97 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 0.97 |
| fbiC | 1303705 | c.775_777delCTGinsTTA | synonymous_variant | 0.97 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 0.97 |
| fbiC | 1303731 | c.801A>G | synonymous_variant | 0.98 |
| fbiC | 1303732 | p.Ser268His | missense_variant | 0.98 |
| fbiC | 1303740 | c.810C>T | synonymous_variant | 0.98 |
| fbiC | 1303746 | p.Asp272Glu | missense_variant | 0.98 |
| fbiC | 1303749 | c.819G>A | synonymous_variant | 0.98 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 0.98 |
| fbiC | 1303764 | c.834C>T | synonymous_variant | 0.98 |
| fbiC | 1303785 | c.855G>T | synonymous_variant | 0.96 |
| fbiC | 1303788 | c.858T>C | synonymous_variant | 0.95 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 0.95 |
| fbiC | 1303797 | c.867A>G | synonymous_variant | 0.95 |
| fbiC | 1303815 | c.885C>T | synonymous_variant | 0.92 |
| fbiC | 1303818 | c.888C>T | synonymous_variant | 0.9 |
| fbiC | 1303833 | c.903C>G | synonymous_variant | 0.92 |
| fbiC | 1303845 | c.915C>G | synonymous_variant | 0.83 |
| fbiC | 1303846 | p.Phe306Met | missense_variant | 0.8 |
| fbiC | 1303854 | c.924T>C | synonymous_variant | 0.8 |
| fbiC | 1303860 | c.930A>C | synonymous_variant | 0.8 |
| fbiC | 1303866 | p.Glu312Asp | missense_variant | 1.0 |
| fbiC | 1303869 | c.939T>C | synonymous_variant | 1.0 |
| fbiC | 1303871 | p.Tyr314Phe | missense_variant | 1.0 |
| fbiC | 1303878 | c.948G>C | synonymous_variant | 1.0 |
| fbiC | 1303881 | c.951G>C | synonymous_variant | 1.0 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 1.0 |
| fbiC | 1303905 | c.975G>C | synonymous_variant | 1.0 |
| fbiC | 1303911 | c.981G>T | synonymous_variant | 1.0 |
| fbiC | 1303920 | c.990C>T | synonymous_variant | 1.0 |
| fbiC | 1303923 | c.993C>T | synonymous_variant | 1.0 |
| fbiC | 1303932 | c.1002G>C | synonymous_variant | 1.0 |
| fbiC | 1303947 | c.1017T>G | synonymous_variant | 1.0 |
| fbiC | 1303949 | p.Gly340Ala | missense_variant | 1.0 |
| fbiC | 1303953 | c.1023C>T | synonymous_variant | 1.0 |
| fbiC | 1303961 | p.Arg344Leu | missense_variant | 1.0 |
| fbiC | 1303969 | p.Val347Ile | missense_variant | 1.0 |
| fbiC | 1303973 | p.Gly348Ala | missense_variant | 1.0 |
| fbiC | 1303998 | c.1068T>C | synonymous_variant | 1.0 |
| fbiC | 1304004 | c.1074A>G | synonymous_variant | 1.0 |
| fbiC | 1304008 | c.1078T>C | synonymous_variant | 1.0 |
| fbiC | 1304013 | c.1083G>C | synonymous_variant | 1.0 |
| fbiC | 1304016 | c.1086C>T | synonymous_variant | 1.0 |
| fbiC | 1304022 | c.1092T>C | synonymous_variant | 1.0 |
| fbiC | 1304034 | c.1104A>G | synonymous_variant | 1.0 |
| fbiC | 1304058 | p.Glu376Asp | missense_variant | 1.0 |
| fbiC | 1304064 | c.1134G>C | synonymous_variant | 1.0 |
| fbiC | 1304067 | c.1137G>C | synonymous_variant | 1.0 |
| fbiC | 1304079 | c.1149A>G | synonymous_variant | 1.0 |
| fbiC | 1304082 | c.1152C>G | synonymous_variant | 1.0 |
| fbiC | 1304092 | p.Met388Leu | missense_variant | 1.0 |
| fbiC | 1304098 | p.Gln390Glu | 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>T | synonymous_variant | 1.0 |
| fbiC | 1304133 | c.1203G>C | synonymous_variant | 1.0 |
| fbiC | 1304136 | c.1206C>G | synonymous_variant | 1.0 |
| fbiC | 1304142 | c.1212G>C | synonymous_variant | 1.0 |
| fbiC | 1304161 | p.Arg411Ala | missense_variant | 1.0 |
| fbiC | 1304172 | c.1242G>T | synonymous_variant | 1.0 |
| fbiC | 1304174 | p.Val415Ala | missense_variant | 1.0 |
| fbiC | 1304184 | c.1254G>C | synonymous_variant | 1.0 |
| fbiC | 1304192 | p.Ala421Gly | missense_variant | 1.0 |
| fbiC | 1304199 | c.1269C>G | synonymous_variant | 1.0 |
| fbiC | 1304211 | c.1281C>T | synonymous_variant | 1.0 |
| fbiC | 1304217 | p.Asn429Lys | missense_variant | 1.0 |
| fbiC | 1304232 | c.1302G>C | synonymous_variant | 1.0 |
| fbiC | 1304259 | c.1329C>G | synonymous_variant | 1.0 |
| fbiC | 1304508 | p.Glu526Asp | missense_variant | 1.0 |
| fbiC | 1304511 | c.1581C>T | synonymous_variant | 1.0 |
| fbiC | 1304517 | c.1587C>T | synonymous_variant | 1.0 |
| fbiC | 1304533 | c.1603T>C | synonymous_variant | 1.0 |
| fbiC | 1304544 | p.Asp538Glu | missense_variant | 1.0 |
| fbiC | 1304546 | p.Val539Ala | missense_variant | 1.0 |
| fbiC | 1304553 | c.1623C>T | synonymous_variant | 1.0 |
| fbiC | 1304556 | c.1626C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304604 | c.1674C>T | synonymous_variant | 0.98 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.98 |
| fbiC | 1304619 | c.1689G>A | synonymous_variant | 0.97 |
| fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.97 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.97 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.97 |
| fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.94 |
| fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.9 |
| fbiC | 1304688 | p.Asp586Glu | missense_variant | 0.75 |
| fbiC | 1304691 | c.1761G>T | synonymous_variant | 0.75 |
| fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.75 |
| fbiC | 1304703 | c.1773C>A | synonymous_variant | 0.75 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.75 |
| fbiC | 1304718 | c.1788C>G | synonymous_variant | 0.75 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.75 |
| fbiC | 1304727 | c.1797A>C | synonymous_variant | 0.75 |
| fbiC | 1304730 | c.1800C>T | synonymous_variant | 0.75 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.8 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304774 | p.Ala615Val | missense_variant | 1.0 |
| fbiC | 1304784 | c.1854T>G | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>C | synonymous_variant | 1.0 |
| fbiC | 1304790 | c.1860C>G | synonymous_variant | 1.0 |
| fbiC | 1304797 | p.Ala623Thr | missense_variant | 1.0 |
| fbiC | 1304811 | c.1881C>G | synonymous_variant | 1.0 |
| fbiC | 1304826 | c.1896G>C | synonymous_variant | 1.0 |
| fbiC | 1304855 | p.Val642Ala | missense_variant | 1.0 |
| fbiC | 1304870 | c.1941_1945delGAGCA | frameshift_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304906 | p.Ala659Gly | missense_variant | 1.0 |
| fbiC | 1304910 | c.1980G>A | synonymous_variant | 1.0 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 1.0 |
| fbiC | 1304922 | c.1992C>A | synonymous_variant | 1.0 |
| fbiC | 1304925 | c.1995G>C | synonymous_variant | 1.0 |
| fbiC | 1304934 | c.2004C>G | synonymous_variant | 1.0 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 1.0 |
| fbiC | 1304955 | c.2025G>A | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
| fbiC | 1304961 | c.2031C>T | synonymous_variant | 1.0 |
| fbiC | 1304970 | c.2040G>C | synonymous_variant | 1.0 |
| fbiC | 1304988 | c.2058G>C | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | p.Leu689Met | missense_variant | 1.0 |
| fbiC | 1305006 | p.Glu692Asp | missense_variant | 1.0 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 1.0 |
| fbiC | 1305021 | c.2091C>G | synonymous_variant | 1.0 |
| fbiC | 1305033 | c.2103T>G | synonymous_variant | 1.0 |
| fbiC | 1305042 | c.2112A>G | synonymous_variant | 1.0 |
| fbiC | 1305045 | c.2115A>G | synonymous_variant | 1.0 |
| fbiC | 1305069 | c.2139G>C | synonymous_variant | 1.0 |
| fbiC | 1305075 | c.2145T>C | synonymous_variant | 1.0 |
| fbiC | 1305078 | c.2148A>G | synonymous_variant | 1.0 |
| fbiC | 1305092 | p.Ala721Gly | missense_variant | 1.0 |
| fbiC | 1305099 | c.2169T>C | synonymous_variant | 1.0 |
| fbiC | 1305102 | p.Asn724Lys | missense_variant | 1.0 |
| fbiC | 1305106 | c.2176C>T | synonymous_variant | 1.0 |
| fbiC | 1305114 | c.2184T>C | synonymous_variant | 1.0 |
| fbiC | 1305117 | c.2187T>C | synonymous_variant | 1.0 |
| fbiC | 1305126 | c.2196T>C | synonymous_variant | 1.0 |
| fbiC | 1305129 | c.2199C>T | synonymous_variant | 1.0 |
| fbiC | 1305132 | c.2202C>A | synonymous_variant | 1.0 |
| fbiC | 1305135 | c.2205C>A | 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>G | 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 | 1305199 | p.Ala757Ser | missense_variant | 1.0 |
| fbiC | 1305204 | c.2274C>G | synonymous_variant | 1.0 |
| fbiC | 1305313 | p.Arg795Gly | missense_variant | 1.0 |
| fbiC | 1305318 | c.2388C>G | synonymous_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305369 | c.2439G>A | synonymous_variant | 1.0 |
| fbiC | 1305375 | c.2445C>G | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>C | synonymous_variant | 1.0 |
| fbiC | 1305420 | c.2490C>G | synonymous_variant | 1.0 |
| fbiC | 1305421 | p.Ala831Pro | missense_variant | 1.0 |
| fbiC | 1305444 | c.2514A>G | synonymous_variant | 1.0 |
| fbiC | 1305456 | c.2526C>G | synonymous_variant | 1.0 |
| fbiC | 1305459 | c.2529G>C | synonymous_variant | 1.0 |
| fbiC | 1305465 | c.2535C>T | synonymous_variant | 1.0 |
| fbiC | 1305474 | c.2544T>C | synonymous_variant | 0.94 |
| fbiC | 1305480 | c.2550A>C | synonymous_variant | 0.93 |
| fbiC | 1305488 | p.Leu853Pro | missense_variant | 0.75 |
| fbiC | 1305492 | c.2562T>C | synonymous_variant | 0.75 |
| atpE | 1460849 | c.-196G>A | upstream_gene_variant | 0.89 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 0.86 |
| atpE | 1460858 | c.-187C>G | upstream_gene_variant | 0.67 |
| atpE | 1460876 | c.-169G>A | upstream_gene_variant | 1.0 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1460885 | c.-160G>C | upstream_gene_variant | 1.0 |
| atpE | 1460900 | c.-145T>C | upstream_gene_variant | 0.67 |
| atpE | 1460904 | c.-141C>T | upstream_gene_variant | 0.67 |
| atpE | 1460915 | c.-130C>A | upstream_gene_variant | 0.67 |
| atpE | 1460916 | c.-129_-128delGCinsCT | upstream_gene_variant | 0.67 |
| atpE | 1460933 | c.-112T>C | upstream_gene_variant | 0.67 |
| atpE | 1460936 | c.-109T>C | upstream_gene_variant | 0.67 |
| atpE | 1460940 | c.-105C>T | upstream_gene_variant | 0.67 |
| atpE | 1460948 | c.-97A>C | upstream_gene_variant | 0.67 |
| atpE | 1460951 | c.-94T>C | upstream_gene_variant | 0.67 |
| atpE | 1461042 | c.-2_-1delAA | upstream_gene_variant | 0.91 |
| atpE | 1461048 | p.Asp2Asn | missense_variant | 0.91 |
| atpE | 1461074 | c.30C>T | synonymous_variant | 1.0 |
| atpE | 1461093 | p.Met17Leu | missense_variant | 1.0 |
| atpE | 1461097 | p.Ala18Gly | missense_variant | 1.0 |
| atpE | 1461108 | p.Ile22Val | missense_variant | 1.0 |
| atpE | 1461118 | p.Gly25Ala | missense_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 0.98 |
| atpE | 1461161 | c.117C>T | synonymous_variant | 1.0 |
| atpE | 1461167 | c.123G>C | synonymous_variant | 1.0 |
| atpE | 1461173 | c.129C>T | synonymous_variant | 1.0 |
| atpE | 1461176 | c.132G>A | synonymous_variant | 1.0 |
| atpE | 1461179 | c.135G>A | synonymous_variant | 1.0 |
| atpE | 1461182 | c.138A>G | synonymous_variant | 0.97 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461212 | c.168C>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>G | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461261 | c.217C>T | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>C | synonymous_variant | 1.0 |
| atpE | 1461281 | c.237C>A | synonymous_variant | 1.0 |
| rrs | 1471843 | n.-3_-2insAA | upstream_gene_variant | 0.67 |
| rrs | 1471922 | n.77_78insC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472027 | n.182C>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.96 |
| rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472298 | n.453G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472302 | n.457G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472304 | n.459G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472309 | n.464C>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016_1017insGT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1473637 | n.-21A>T | upstream_gene_variant | 1.0 |
| rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1473670 | n.13A>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1473701 | n.44A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473782 | n.125A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.86 |
| 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 | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474286 | n.630delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474290 | n.633T>G | non_coding_transcript_exon_variant | 0.47 |
| rrl | 1474292 | n.636_649delTCCTCTCCGGAGGA | 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 | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474417 | n.760A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474422 | n.765C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474424 | n.767C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474426 | n.769T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474427 | n.771_773delCGC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474715 | n.1058T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474716 | n.1059A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475030 | n.1373_1374insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475217 | n.1560T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475232 | n.1575A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475257 | n.1600C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475276 | n.1619T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475277 | n.1620G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475278 | n.1621G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475291 | n.1634A>T | 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 | 1475378 | n.1721A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475379 | n.1722G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475413 | n.1756A>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475484 | n.1827A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.95 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476246 | n.2589G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476689 | n.3033delC | 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 | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673565 | c.-637G>C | upstream_gene_variant | 1.0 |
| inhA | 1673568 | c.-634C>G | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673580 | c.-622T>C | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>G | upstream_gene_variant | 1.0 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673596 | p.Lys53Asp | missense_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| inhA | 1673616 | c.-586A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| inhA | 1673640 | c.-562C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673685 | c.-517C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673698 | p.Ser87Ala | missense_variant | 1.0 |
| inhA | 1673712 | c.-490A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673713 | p.Ser92Ala | missense_variant | 1.0 |
| inhA | 1673724 | c.-478A>G | upstream_gene_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673756 | p.Glu106Val | missense_variant | 1.0 |
| fabG1 | 1673767 | p.Asn110Asp | missense_variant | 1.0 |
| inhA | 1673781 | c.-421C>T | upstream_gene_variant | 1.0 |
| inhA | 1673790 | c.-412C>T | upstream_gene_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673826 | c.-376C>G | 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>G | upstream_gene_variant | 1.0 |
| inhA | 1673847 | c.-355A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673853 | p.Ile138Met | missense_variant | 1.0 |
| inhA | 1673862 | c.-340C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673870 | p.Ser144Thr | missense_variant | 1.0 |
| inhA | 1673898 | c.-304C>T | upstream_gene_variant | 1.0 |
| inhA | 1673916 | c.-286A>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673917 | p.Val160Leu | missense_variant | 1.0 |
| inhA | 1673922 | c.-280T>C | upstream_gene_variant | 1.0 |
| inhA | 1673949 | c.-253G>A | upstream_gene_variant | 1.0 |
| inhA | 1673955 | c.-247G>A | upstream_gene_variant | 1.0 |
| inhA | 1673958 | c.-244G>A | upstream_gene_variant | 1.0 |
| inhA | 1673961 | c.-241A>C | upstream_gene_variant | 1.0 |
| inhA | 1673964 | c.-238C>T | upstream_gene_variant | 1.0 |
| inhA | 1673976 | c.-226T>C | upstream_gene_variant | 1.0 |
| inhA | 1673985 | c.-217C>A | upstream_gene_variant | 1.0 |
| inhA | 1674006 | c.-196T>C | upstream_gene_variant | 1.0 |
| inhA | 1674012 | c.-190C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674037 | p.Gln200Ala | missense_variant | 1.0 |
| inhA | 1674042 | c.-160G>C | upstream_gene_variant | 1.0 |
| inhA | 1674045 | c.-157G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1674049 | p.Gln204Asp | missense_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| inhA | 1674063 | c.-139G>A | upstream_gene_variant | 1.0 |
| inhA | 1674078 | c.-124C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| fabG1 | 1674083 | p.Ala215Glu | missense_variant | 1.0 |
| inhA | 1674120 | c.-82G>A | upstream_gene_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>C | upstream_gene_variant | 1.0 |
| inhA | 1674127 | c.-75_-73delAGCinsTCA | 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 |
| inhA | 1674141 | c.-61T>C | upstream_gene_variant | 1.0 |
| inhA | 1674147 | c.-55C>G | upstream_gene_variant | 1.0 |
| inhA | 1674171 | c.-31T>C | upstream_gene_variant | 1.0 |
| inhA | 1674177 | c.-25C>T | upstream_gene_variant | 1.0 |
| inhA | 1674182 | c.-20G>A | upstream_gene_variant | 1.0 |
| inhA | 1674256 | p.Ser19Ala | missense_variant | 0.67 |
| inhA | 1674270 | c.69T>C | synonymous_variant | 0.67 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 0.67 |
| inhA | 1674443 | p.Ala81Val | missense_variant | 0.75 |
| inhA | 1674450 | c.249G>C | synonymous_variant | 0.75 |
| inhA | 1674452 | p.Ala84Glu | missense_variant | 0.75 |
| inhA | 1674465 | c.264C>T | synonymous_variant | 0.92 |
| 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 | 1674500 | p.Gln100Pro | missense_variant | 1.0 |
| inhA | 1674503 | p.Thr101Ser | missense_variant | 1.0 |
| inhA | 1674531 | p.Asp110Glu | missense_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 | 1674576 | c.375T>C | synonymous_variant | 1.0 |
| inhA | 1674579 | c.378G>C | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>A | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674601 | p.Leu134Val | missense_variant | 1.0 |
| inhA | 1674609 | c.408G>C | synonymous_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674620 | p.Pro140Arg | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>T | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674628 | p.Ser143Gly | missense_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674669 | c.468G>C | synonymous_variant | 1.0 |
| inhA | 1674690 | c.489C>G | synonymous_variant | 1.0 |
| inhA | 1674702 | c.501G>A | synonymous_variant | 0.96 |
| inhA | 1674703 | c.502_504delTTGinsCTC | synonymous_variant | 0.96 |
| inhA | 1674714 | c.513C>G | synonymous_variant | 0.96 |
| inhA | 1674718 | c.517_519delAGGinsCGC | synonymous_variant | 0.96 |
| inhA | 1674726 | c.525G>C | synonymous_variant | 0.96 |
| inhA | 1674729 | c.528G>C | synonymous_variant | 0.96 |
| inhA | 1674742 | p.Lys181Pro | missense_variant | 0.96 |
| inhA | 1674756 | c.555T>A | synonymous_variant | 0.93 |
| inhA | 1674759 | c.558G>C | synonymous_variant | 0.93 |
| inhA | 1674774 | c.573A>C | synonymous_variant | 0.8 |
| inhA | 1674777 | c.576C>A | synonymous_variant | 0.8 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 0.8 |
| inhA | 1674783 | c.582C>T | synonymous_variant | 0.8 |
| inhA | 1674792 | c.591G>C | synonymous_variant | 0.8 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 0.9 |
| inhA | 1674813 | c.612C>A | synonymous_variant | 0.91 |
| inhA | 1674816 | c.615T>G | synonymous_variant | 0.91 |
| inhA | 1674835 | p.Gly212Ser | missense_variant | 0.83 |
| inhA | 1674839 | p.Ala213Gly | missense_variant | 0.83 |
| inhA | 1674846 | p.Ile215Met | missense_variant | 0.83 |
| inhA | 1674859 | p.Glu220Gln | missense_variant | 0.86 |
| inhA | 1674864 | c.663C>T | synonymous_variant | 0.86 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 0.86 |
| inhA | 1674876 | c.675C>A | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>G | synonymous_variant | 1.0 |
| inhA | 1674892 | p.Asn231Asp | missense_variant | 1.0 |
| inhA | 1674900 | c.699G>A | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674906 | c.705G>C | synonymous_variant | 1.0 |
| inhA | 1674912 | c.711G>C | synonymous_variant | 1.0 |
| inhA | 1674915 | c.714C>T | synonymous_variant | 1.0 |
| inhA | 1674921 | c.720G>A | synonymous_variant | 1.0 |
| inhA | 1674927 | c.726G>A | synonymous_variant | 1.0 |
| inhA | 1674934 | p.Leu245Val | missense_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674957 | c.756G>C | synonymous_variant | 1.0 |
| inhA | 1674963 | c.762G>C | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>C | synonymous_variant | 1.0 |
| inhA | 1674990 | c.789C>G | synonymous_variant | 1.0 |
| inhA | 1674996 | c.795C>T | synonymous_variant | 1.0 |
| inhA | 1674998 | p.Thr266Asn | missense_variant | 1.0 |
| rpsA | 1833516 | c.-26A>C | upstream_gene_variant | 0.82 |
| rpsA | 1833518 | c.-24C>A | upstream_gene_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>A | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833622 | c.81C>T | synonymous_variant | 1.0 |
| rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
| rpsA | 1833628 | c.87G>A | synonymous_variant | 1.0 |
| rpsA | 1833634 | c.93G>A | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833670 | c.129C>A | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833688 | c.147C>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 0.98 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833778 | c.237C>G | synonymous_variant | 1.0 |
| rpsA | 1833781 | c.240T>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833794 | p.Glu85Lys | missense_variant | 0.98 |
| rpsA | 1833797 | p.Val86Ile | missense_variant | 0.98 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 0.98 |
| rpsA | 1833806 | c.265C>T | synonymous_variant | 0.98 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 0.98 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 0.98 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 0.98 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833892 | c.351G>A | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>G | synonymous_variant | 1.0 |
| rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
| rpsA | 1833971 | c.430C>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>T | synonymous_variant | 0.98 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834024 | c.483G>T | synonymous_variant | 1.0 |
| rpsA | 1834069 | c.528G>C | synonymous_variant | 0.98 |
| rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.97 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 0.97 |
| rpsA | 1834105 | c.564C>G | synonymous_variant | 1.0 |
| rpsA | 1834123 | c.582C>G | synonymous_variant | 1.0 |
| rpsA | 1834126 | c.585G>A | synonymous_variant | 1.0 |
| rpsA | 1834135 | c.594G>C | 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 | 1834162 | c.621A>G | 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 | 1834183 | c.642T>C | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
| rpsA | 1834192 | c.651C>T | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834262 | c.721_723delTCGinsAGT | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>G | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 0.98 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>G | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834447 | c.906C>T | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910_912delTTGinsCTT | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834531 | c.990C>T | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834557 | p.Ala339Gly | missense_variant | 1.0 |
| rpsA | 1834573 | c.1032G>A | synonymous_variant | 1.0 |
| rpsA | 1834582 | c.1041G>A | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834615 | c.1074C>T | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834669 | c.1128G>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834755 | p.Glu405Ala | missense_variant | 1.0 |
| rpsA | 1834759 | c.1218A>T | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834766 | p.Lys409Ala | missense_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>C | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834828 | c.1287C>G | synonymous_variant | 1.0 |
| rpsA | 1834852 | c.1311C>G | synonymous_variant | 1.0 |
| rpsA | 1834866 | p.Gly442Ala | missense_variant | 1.0 |
| tlyA | 1917965 | p.Ala9Val | missense_variant | 1.0 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 0.82 |
| tlyA | 1917984 | c.45C>G | synonymous_variant | 1.0 |
| tlyA | 1917991 | c.52C>A | synonymous_variant | 0.92 |
| tlyA | 1917996 | c.57A>G | synonymous_variant | 0.92 |
| tlyA | 1917999 | c.60T>C | synonymous_variant | 0.92 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 0.92 |
| tlyA | 1918008 | c.69C>T | synonymous_variant | 0.93 |
| tlyA | 1918036 | p.Arg33Ser | missense_variant | 0.93 |
| tlyA | 1918047 | c.108G>C | synonymous_variant | 1.0 |
| tlyA | 1918048 | p.Leu37Met | missense_variant | 1.0 |
| tlyA | 1918053 | c.114G>T | synonymous_variant | 1.0 |
| tlyA | 1918062 | c.123G>A | synonymous_variant | 1.0 |
| tlyA | 1918065 | c.126G>C | synonymous_variant | 1.0 |
| tlyA | 1918395 | c.456G>C | synonymous_variant | 1.0 |
| tlyA | 1918417 | c.478T>C | synonymous_variant | 1.0 |
| tlyA | 1918420 | p.Ala161Thr | missense_variant | 1.0 |
| tlyA | 1918425 | c.486C>G | synonymous_variant | 1.0 |
| tlyA | 1918438 | c.499C>T | synonymous_variant | 1.0 |
| tlyA | 1918441 | p.Val168Ile | missense_variant | 1.0 |
| tlyA | 1918446 | c.507A>C | synonymous_variant | 1.0 |
| tlyA | 1918449 | c.510C>T | synonymous_variant | 1.0 |
| tlyA | 1918452 | c.513T>G | synonymous_variant | 1.0 |
| tlyA | 1918457 | p.Arg173Pro | missense_variant | 1.0 |
| tlyA | 1918464 | c.525C>A | synonymous_variant | 1.0 |
| tlyA | 1918470 | c.531C>T | synonymous_variant | 1.0 |
| tlyA | 1918476 | c.537A>C | synonymous_variant | 1.0 |
| tlyA | 1918477 | p.Leu180Met | missense_variant | 1.0 |
| tlyA | 1918494 | c.555T>C | synonymous_variant | 1.0 |
| ndh | 2102192 | p.Arg284Pro | missense_variant | 1.0 |
| ndh | 2102194 | c.849T>C | synonymous_variant | 1.0 |
| ndh | 2102203 | c.840T>C | synonymous_variant | 1.0 |
| ndh | 2102218 | c.825C>G | synonymous_variant | 1.0 |
| ndh | 2102233 | c.810G>A | synonymous_variant | 1.0 |
| ndh | 2102239 | c.804C>A | synonymous_variant | 1.0 |
| ndh | 2102246 | p.Val266Thr | missense_variant | 1.0 |
| ndh | 2102248 | c.795C>T | synonymous_variant | 1.0 |
| ndh | 2102251 | c.792C>A | synonymous_variant | 1.0 |
| ndh | 2102257 | p.Ser262Pro | missense_variant | 1.0 |
| ndh | 2102269 | c.774C>G | synonymous_variant | 1.0 |
| ndh | 2102305 | c.738T>C | synonymous_variant | 1.0 |
| ndh | 2102359 | c.684C>G | synonymous_variant | 1.0 |
| ndh | 2102366 | p.Ala226Glu | missense_variant | 1.0 |
| ndh | 2102377 | c.666A>G | synonymous_variant | 1.0 |
| ndh | 2102389 | c.654G>C | synonymous_variant | 1.0 |
| ndh | 2102392 | c.651C>G | synonymous_variant | 1.0 |
| ndh | 2102401 | c.642T>C | synonymous_variant | 1.0 |
| ndh | 2102407 | c.636T>C | synonymous_variant | 1.0 |
| ndh | 2102410 | c.633G>C | synonymous_variant | 1.0 |
| ndh | 2102427 | p.Ser206Pro | missense_variant | 1.0 |
| ndh | 2102460 | p.His195Tyr | missense_variant | 0.97 |
| ndh | 2102469 | c.574C>T | synonymous_variant | 1.0 |
| ndh | 2102470 | c.573G>A | synonymous_variant | 1.0 |
| ndh | 2102482 | c.561A>G | synonymous_variant | 1.0 |
| ndh | 2102494 | c.549T>C | synonymous_variant | 1.0 |
| ndh | 2102497 | c.546T>C | synonymous_variant | 1.0 |
| ndh | 2102506 | c.537C>T | synonymous_variant | 1.0 |
| ndh | 2102509 | c.534T>C | synonymous_variant | 1.0 |
| ndh | 2102518 | c.525T>C | synonymous_variant | 1.0 |
| ndh | 2102527 | c.516A>C | synonymous_variant | 1.0 |
| ndh | 2102530 | c.513G>C | synonymous_variant | 1.0 |
| ndh | 2102548 | c.495A>G | synonymous_variant | 1.0 |
| ndh | 2102558 | p.Ser162Asn | missense_variant | 1.0 |
| ndh | 2102566 | c.477A>G | synonymous_variant | 1.0 |
| ndh | 2102572 | c.471A>G | synonymous_variant | 1.0 |
| ndh | 2102581 | c.462T>G | synonymous_variant | 1.0 |
| ndh | 2102587 | c.454_456delTTGinsCTC | synonymous_variant | 1.0 |
| ndh | 2102590 | c.453A>C | synonymous_variant | 1.0 |
| ndh | 2102599 | c.444T>G | synonymous_variant | 1.0 |
| ndh | 2102604 | c.439T>C | synonymous_variant | 1.0 |
| ndh | 2102610 | c.433T>C | synonymous_variant | 1.0 |
| ndh | 2102623 | c.420C>G | synonymous_variant | 1.0 |
| ndh | 2102644 | c.399A>G | synonymous_variant | 1.0 |
| ndh | 2102653 | c.390T>C | synonymous_variant | 1.0 |
| ndh | 2102668 | c.375T>C | synonymous_variant | 1.0 |
| ndh | 2102671 | c.372T>C | synonymous_variant | 1.0 |
| ndh | 2102677 | c.366C>G | synonymous_variant | 1.0 |
| ndh | 2102680 | c.363T>G | synonymous_variant | 1.0 |
| ndh | 2102683 | c.360T>C | synonymous_variant | 1.0 |
| ndh | 2102686 | c.357G>C | synonymous_variant | 1.0 |
| ndh | 2102694 | p.Val117Ile | missense_variant | 1.0 |
| ndh | 2102710 | p.Pro111His | missense_variant | 1.0 |
| ndh | 2102718 | p.Gln109Glu | missense_variant | 1.0 |
| ndh | 2102728 | c.315T>C | synonymous_variant | 1.0 |
| ndh | 2102737 | c.306A>G | synonymous_variant | 1.0 |
| katG | 2155251 | c.861A>G | synonymous_variant | 1.0 |
| katG | 2155257 | c.855C>T | synonymous_variant | 1.0 |
| katG | 2155263 | c.849G>C | synonymous_variant | 1.0 |
| katG | 2155272 | p.Pro280Asp | missense_variant | 1.0 |
| katG | 2155281 | c.831C>T | synonymous_variant | 1.0 |
| katG | 2155284 | c.828T>C | synonymous_variant | 1.0 |
| katG | 2155293 | c.819T>C | synonymous_variant | 1.0 |
| katG | 2155298 | p.Phe272Val | missense_variant | 1.0 |
| katG | 2155299 | c.813T>C | synonymous_variant | 1.0 |
| katG | 2155305 | c.807T>C | synonymous_variant | 1.0 |
| katG | 2155326 | c.786A>G | synonymous_variant | 1.0 |
| katG | 2155329 | c.783A>G | synonymous_variant | 1.0 |
| katG | 2155344 | c.768C>G | synonymous_variant | 1.0 |
| katG | 2155350 | c.762C>G | synonymous_variant | 1.0 |
| katG | 2155353 | p.Arg253Gly | missense_variant | 0.83 |
| katG | 2155356 | c.756T>C | synonymous_variant | 1.0 |
| katG | 2155365 | c.747C>G | synonymous_variant | 1.0 |
| katG | 2155368 | c.744T>C | synonymous_variant | 1.0 |
| katG | 2155376 | p.Val246Ile | missense_variant | 1.0 |
| katG | 2155626 | c.486G>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 1.0 |
| katG | 2155641 | p.Lys157Ser | missense_variant | 1.0 |
| katG | 2155656 | c.456G>A | synonymous_variant | 1.0 |
| katG | 2155662 | c.450G>C | synonymous_variant | 1.0 |
| katG | 2155668 | c.444G>C | synonymous_variant | 1.0 |
| katG | 2155673 | c.439C>T | synonymous_variant | 1.0 |
| katG | 2155689 | c.421_423delTTGinsCTA | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155735 | p.Met126Ser | missense_variant | 1.0 |
| katG | 2155740 | p.Gly124Glu | missense_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| katG | 2155747 | p.Ala122Gly | missense_variant | 1.0 |
| katG | 2155758 | c.354C>T | synonymous_variant | 1.0 |
| katG | 2155764 | c.348C>T | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155788 | c.324C>T | synonymous_variant | 1.0 |
| katG | 2155794 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155815 | c.297G>A | synonymous_variant | 1.0 |
| katG | 2155836 | c.276C>G | synonymous_variant | 1.0 |
| katG | 2155845 | p.Pro89Asp | missense_variant | 1.0 |
| katG | 2155854 | c.258C>A | synonymous_variant | 1.0 |
| kasA | 2517917 | c.-198G>T | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2517994 | c.-121_-120delCCinsAG | 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 | 2518028 | c.-87G>A | upstream_gene_variant | 1.0 |
| kasA | 2518034 | c.-81T>C | upstream_gene_variant | 1.0 |
| kasA | 2518040 | c.-75G>C | upstream_gene_variant | 1.0 |
| kasA | 2518041 | c.-74_-72delTTGinsATC | upstream_gene_variant | 1.0 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 1.0 |
| kasA | 2518055 | c.-60T>C | upstream_gene_variant | 1.0 |
| kasA | 2518059 | c.-56T>G | upstream_gene_variant | 1.0 |
| kasA | 2518070 | c.-45C>G | upstream_gene_variant | 1.0 |
| kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
| kasA | 2518138 | c.24T>C | synonymous_variant | 1.0 |
| kasA | 2518162 | c.48G>A | synonymous_variant | 1.0 |
| kasA | 2518174 | c.60A>G | synonymous_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 1.0 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518267 | c.153C>G | synonymous_variant | 1.0 |
| kasA | 2518279 | c.165T>C | synonymous_variant | 1.0 |
| kasA | 2518282 | c.168A>G | synonymous_variant | 1.0 |
| kasA | 2518283 | p.Ala57Pro | missense_variant | 1.0 |
| kasA | 2518312 | p.Asp66Glu | missense_variant | 1.0 |
| kasA | 2518313 | p.Pro67Ala | missense_variant | 1.0 |
| kasA | 2518322 | p.Ser70Asp | missense_variant | 1.0 |
| kasA | 2518333 | c.219C>T | synonymous_variant | 1.0 |
| kasA | 2518336 | c.222A>G | synonymous_variant | 1.0 |
| kasA | 2518343 | p.Met77Leu | missense_variant | 1.0 |
| kasA | 2518348 | c.234A>G | synonymous_variant | 1.0 |
| kasA | 2518360 | c.246C>T | synonymous_variant | 1.0 |
| kasA | 2518417 | c.303G>C | synonymous_variant | 1.0 |
| kasA | 2518426 | c.312T>C | synonymous_variant | 1.0 |
| kasA | 2518429 | c.315A>C | synonymous_variant | 1.0 |
| kasA | 2518432 | c.318C>T | synonymous_variant | 1.0 |
| kasA | 2518444 | c.330T>C | synonymous_variant | 1.0 |
| kasA | 2518447 | c.333T>C | synonymous_variant | 1.0 |
| kasA | 2518448 | p.Val112Ile | missense_variant | 1.0 |
| kasA | 2518462 | c.348A>G | synonymous_variant | 1.0 |
| kasA | 2518468 | c.354A>C | synonymous_variant | 1.0 |
| kasA | 2518475 | c.361A>C | synonymous_variant | 1.0 |
| kasA | 2518486 | c.372G>A | synonymous_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
| kasA | 2518528 | c.414C>G | synonymous_variant | 1.0 |
| kasA | 2518531 | c.417G>A | synonymous_variant | 0.97 |
| kasA | 2518540 | c.426T>C | synonymous_variant | 1.0 |
| kasA | 2518561 | c.447T>C | synonymous_variant | 1.0 |
| kasA | 2518564 | c.450C>T | synonymous_variant | 1.0 |
| kasA | 2518571 | p.Val153Thr | missense_variant | 1.0 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
| kasA | 2518588 | c.474T>G | synonymous_variant | 0.97 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518597 | c.483C>T | synonymous_variant | 1.0 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
| kasA | 2518636 | c.522C>T | synonymous_variant | 1.0 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
| kasA | 2518645 | c.531G>C | synonymous_variant | 1.0 |
| kasA | 2518651 | c.537C>G | synonymous_variant | 1.0 |
| kasA | 2518657 | c.543G>C | synonymous_variant | 1.0 |
| kasA | 2518663 | c.549T>G | synonymous_variant | 1.0 |
| kasA | 2518666 | c.552G>A | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518688 | p.Val192Ile | missense_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518705 | c.591T>C | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518715 | p.Pro201Gly | missense_variant | 1.0 |
| kasA | 2518727 | c.613C>T | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518735 | c.621C>T | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518780 | p.Glu222Asp | missense_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518786 | c.672G>A | synonymous_variant | 1.0 |
| kasA | 2518787 | p.Arg225Gly | missense_variant | 1.0 |
| kasA | 2518792 | c.678C>G | synonymous_variant | 0.95 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 0.91 |
| kasA | 2518798 | c.684G>T | synonymous_variant | 1.0 |
| kasA | 2518801 | c.687G>C | synonymous_variant | 0.93 |
| kasA | 2518822 | c.708C>T | synonymous_variant | 0.92 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518834 | c.720C>T | synonymous_variant | 1.0 |
| kasA | 2518840 | c.726C>G | synonymous_variant | 0.89 |
| kasA | 2518843 | c.729T>C | synonymous_variant | 1.0 |
| kasA | 2518849 | c.735G>C | synonymous_variant | 0.85 |
| kasA | 2518853 | p.Leu247Val | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518894 | c.780G>A | synonymous_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>T | synonymous_variant | 1.0 |
| kasA | 2518907 | c.793T>C | synonymous_variant | 1.0 |
| kasA | 2518921 | c.807T>C | synonymous_variant | 1.0 |
| kasA | 2518927 | c.813C>T | synonymous_variant | 1.0 |
| kasA | 2518930 | c.816G>C | synonymous_variant | 1.0 |
| kasA | 2518939 | c.825T>C | synonymous_variant | 1.0 |
| kasA | 2518942 | c.828T>C | synonymous_variant | 1.0 |
| kasA | 2519049 | p.Gly312Ala | missense_variant | 1.0 |
| kasA | 2519056 | c.942G>C | synonymous_variant | 1.0 |
| kasA | 2519062 | c.948T>G | synonymous_variant | 1.0 |
| kasA | 2519071 | c.957C>T | synonymous_variant | 1.0 |
| kasA | 2519072 | p.Ala320Thr | missense_variant | 1.0 |
| kasA | 2519077 | c.963G>C | synonymous_variant | 1.0 |
| kasA | 2519080 | c.966G>A | synonymous_variant | 1.0 |
| kasA | 2519089 | c.975C>T | synonymous_variant | 1.0 |
| kasA | 2519095 | c.981C>G | synonymous_variant | 1.0 |
| kasA | 2519107 | c.993T>C | synonymous_variant | 1.0 |
| kasA | 2519110 | p.Asp332Glu | missense_variant | 1.0 |
| kasA | 2519115 | p.Ala334Gly | missense_variant | 1.0 |
| kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
| kasA | 2519135 | p.Ser341Gly | missense_variant | 1.0 |
| kasA | 2519146 | c.1032C>T | synonymous_variant | 1.0 |
| kasA | 2519152 | c.1038G>C | synonymous_variant | 1.0 |
| kasA | 2519158 | c.1044C>T | synonymous_variant | 1.0 |
| kasA | 2519161 | c.1047G>C | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>C | synonymous_variant | 1.0 |
| kasA | 2519170 | c.1056G>T | synonymous_variant | 1.0 |
| kasA | 2519171 | c.1057_1059delCTCinsTTG | synonymous_variant | 1.0 |
| kasA | 2519185 | c.1071C>G | synonymous_variant | 1.0 |
| kasA | 2519188 | c.1074G>C | synonymous_variant | 1.0 |
| kasA | 2519215 | c.1101C>T | synonymous_variant | 1.0 |
| kasA | 2519221 | c.1107G>C | synonymous_variant | 1.0 |
| kasA | 2519224 | c.1110C>G | synonymous_variant | 1.0 |
| kasA | 2519234 | p.Glu374His | missense_variant | 1.0 |
| kasA | 2519239 | c.1125A>C | synonymous_variant | 1.0 |
| kasA | 2519242 | c.1128C>T | synonymous_variant | 1.0 |
| kasA | 2519245 | c.1131T>C | synonymous_variant | 1.0 |
| kasA | 2519248 | c.1134C>G | synonymous_variant | 1.0 |
| kasA | 2519257 | c.1143C>T | synonymous_variant | 1.0 |
| kasA | 2519260 | c.1146T>C | synonymous_variant | 1.0 |
| kasA | 2519266 | c.1152C>G | synonymous_variant | 1.0 |
| kasA | 2519281 | c.1167G>C | synonymous_variant | 1.0 |
| kasA | 2519284 | c.1170C>T | synonymous_variant | 1.0 |
| kasA | 2519293 | p.Asp393Glu | missense_variant | 1.0 |
| kasA | 2519297 | p.Arg395Lys | missense_variant | 1.0 |
| kasA | 2519305 | c.1191A>C | synonymous_variant | 1.0 |
| kasA | 2519306 | p.Val398Ile | missense_variant | 1.0 |
| kasA | 2519332 | c.1218C>G | synonymous_variant | 1.0 |
| kasA | 2519338 | c.1224T>C | synonymous_variant | 1.0 |
| kasA | 2519341 | c.1227G>C | synonymous_variant | 1.0 |
| kasA | 2519347 | c.1233T>C | synonymous_variant | 0.91 |
| kasA | 2519350 | c.1236C>G | synonymous_variant | 1.0 |
| kasA | 2519362 | c.1248C>T | synonymous_variant | 1.0 |
| ahpC | 2726204 | c.12A>G | synonymous_variant | 1.0 |
| ahpC | 2726207 | c.15C>G | synonymous_variant | 1.0 |
| ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
| ahpC | 2726213 | c.21C>T | synonymous_variant | 1.0 |
| ahpC | 2726219 | c.27A>G | synonymous_variant | 1.0 |
| ahpC | 2726233 | p.Gln14Arg | missense_variant | 1.0 |
| ahpC | 2726243 | c.51T>G | synonymous_variant | 1.0 |
| ahpC | 2726246 | c.54C>G | synonymous_variant | 1.0 |
| ahpC | 2726252 | c.60C>T | synonymous_variant | 1.0 |
| ahpC | 2726255 | c.63T>C | synonymous_variant | 1.0 |
| ahpC | 2726261 | c.69G>T | synonymous_variant | 1.0 |
| ahpC | 2726264 | c.72C>G | synonymous_variant | 1.0 |
| ahpC | 2726267 | c.75G>A | synonymous_variant | 1.0 |
| ahpC | 2726287 | p.Gly32Glu | missense_variant | 1.0 |
| ahpC | 2726300 | c.108C>G | synonymous_variant | 1.0 |
| ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
| ahpC | 2726307 | p.Thr39Ser | missense_variant | 1.0 |
| ahpC | 2726312 | c.120T>C | synonymous_variant | 1.0 |
| ahpC | 2726318 | p.Glu42Asp | missense_variant | 1.0 |
| ahpC | 2726324 | c.132A>C | synonymous_variant | 1.0 |
| ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
| ahpC | 2726354 | c.162G>C | synonymous_variant | 1.0 |
| ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
| ahpC | 2726366 | c.174G>C | synonymous_variant | 1.0 |
| ahpC | 2726378 | c.186T>G | synonymous_variant | 1.0 |
| ahpC | 2726390 | c.198G>C | synonymous_variant | 1.0 |
| ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
| ahpC | 2726405 | c.213C>G | synonymous_variant | 1.0 |
| ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 0.83 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 0.89 |
| ahpC | 2726591 | c.399C>G | synonymous_variant | 0.9 |
| ahpC | 2726597 | c.405C>G | synonymous_variant | 0.9 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 0.9 |
| ahpC | 2726621 | c.429G>A | synonymous_variant | 0.89 |
| ahpC | 2726627 | c.435G>A | synonymous_variant | 0.89 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 0.91 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 0.97 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 0.97 |
| ahpC | 2726666 | c.474C>G | synonymous_variant | 0.97 |
| ahpC | 2726669 | c.477T>C | synonymous_variant | 0.97 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 0.96 |
| ahpC | 2726681 | c.489A>G | synonymous_variant | 0.96 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 0.96 |
| ahpC | 2726690 | c.498C>T | synonymous_variant | 0.95 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 0.95 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 0.95 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 1.0 |
| folC | 2746528 | c.1071C>G | synonymous_variant | 0.67 |
| folC | 2746534 | c.1065T>C | synonymous_variant | 0.71 |
| folC | 2746561 | c.1038C>G | synonymous_variant | 0.92 |
| folC | 2746564 | c.1035A>G | synonymous_variant | 0.92 |
| folC | 2746584 | c.1015T>C | synonymous_variant | 0.94 |
| folC | 2746609 | c.990T>C | synonymous_variant | 1.0 |
| folC | 2746612 | c.987C>A | synonymous_variant | 1.0 |
| folC | 2746615 | c.984C>G | synonymous_variant | 1.0 |
| folC | 2746631 | p.Gly323Val | missense_variant | 1.0 |
| folC | 2746642 | c.957T>C | synonymous_variant | 1.0 |
| folC | 2746702 | c.897G>T | synonymous_variant | 0.75 |
| folC | 2746708 | c.891C>T | synonymous_variant | 0.75 |
| folC | 2746714 | c.885T>A | synonymous_variant | 0.75 |
| folC | 2746726 | c.871_873delTTGinsCTC | synonymous_variant | 0.75 |
| folC | 2746729 | c.870C>T | synonymous_variant | 0.75 |
| folC | 2746734 | p.Ile289Val | missense_variant | 0.75 |
| folC | 2746741 | c.858C>T | synonymous_variant | 0.75 |
| folC | 2746744 | c.855T>G | synonymous_variant | 0.75 |
| folC | 2746753 | c.846C>G | synonymous_variant | 0.75 |
| folC | 2746764 | c.835C>T | synonymous_variant | 1.0 |
| folC | 2746765 | c.834A>G | synonymous_variant | 1.0 |
| folC | 2746771 | c.828A>G | synonymous_variant | 1.0 |
| folC | 2746777 | c.822T>C | synonymous_variant | 1.0 |
| folC | 2747248 | c.351G>C | synonymous_variant | 1.0 |
| folC | 2747251 | c.348C>T | synonymous_variant | 1.0 |
| folC | 2747263 | c.336C>A | synonymous_variant | 1.0 |
| folC | 2747272 | p.Ser109Ala | missense_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747281 | c.318A>G | synonymous_variant | 1.0 |
| folC | 2747284 | c.315G>C | synonymous_variant | 1.0 |
| folC | 2747287 | 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 | 1.0 |
| folC | 2747317 | c.282C>A | synonymous_variant | 1.0 |
| folC | 2747341 | p.Val86Leu | missense_variant | 1.0 |
| folC | 2747359 | c.240C>G | synonymous_variant | 1.0 |
| folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
| folC | 2747398 | c.201C>T | synonymous_variant | 1.0 |
| folC | 2747407 | c.192T>C | synonymous_variant | 1.0 |
| folC | 2747410 | p.Ser63Gly | missense_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747422 | c.177G>A | synonymous_variant | 1.0 |
| folC | 2747430 | c.169C>T | synonymous_variant | 1.0 |
| folC | 2747442 | c.157T>C | synonymous_variant | 1.0 |
| folC | 2747447 | p.Ser51Ala | missense_variant | 1.0 |
| folC | 2747452 | c.147G>C | synonymous_variant | 1.0 |
| folC | 2747458 | c.141G>C | synonymous_variant | 1.0 |
| folC | 2747467 | p.Asp44Glu | missense_variant | 1.0 |
| folC | 2747706 | c.-108G>C | upstream_gene_variant | 1.0 |
| folC | 2747713 | c.-115C>A | upstream_gene_variant | 1.0 |
| folC | 2747715 | c.-119_-117delTTGinsCTT | upstream_gene_variant | 1.0 |
| folC | 2747726 | c.-128G>A | upstream_gene_variant | 1.0 |
| folC | 2747730 | c.-132G>C | upstream_gene_variant | 1.0 |
| folC | 2747738 | c.-140C>T | upstream_gene_variant | 1.0 |
| folC | 2747739 | c.-141G>A | upstream_gene_variant | 1.0 |
| folC | 2747748 | c.-150C>G | upstream_gene_variant | 1.0 |
| folC | 2747752 | c.-154G>C | upstream_gene_variant | 1.0 |
| folC | 2747754 | c.-156C>T | upstream_gene_variant | 1.0 |
| folC | 2747760 | c.-162G>T | upstream_gene_variant | 1.0 |
| folC | 2747766 | c.-168A>G | upstream_gene_variant | 1.0 |
| folC | 2747787 | c.-190_-189delCCinsAG | upstream_gene_variant | 1.0 |
| folC | 2747790 | c.-192G>C | upstream_gene_variant | 1.0 |
| folC | 2747796 | c.-198C>T | upstream_gene_variant | 1.0 |
| pepQ | 2859414 | c.1005T>C | synonymous_variant | 1.0 |
| pepQ | 2859424 | p.Gly332Asp | missense_variant | 1.0 |
| pepQ | 2859429 | c.990A>G | synonymous_variant | 1.0 |
| pepQ | 2859438 | c.981T>C | synonymous_variant | 1.0 |
| pepQ | 2859675 | p.Glu248Asp | missense_variant | 1.0 |
| pepQ | 2859678 | p.Leu247Arg | missense_variant | 1.0 |
| pepQ | 2859704 | c.715T>C | synonymous_variant | 1.0 |
| pepQ | 2859714 | c.705C>A | synonymous_variant | 1.0 |
| pepQ | 2859732 | c.687C>T | synonymous_variant | 1.0 |
| pepQ | 2859750 | c.669C>T | synonymous_variant | 1.0 |
| pepQ | 2859765 | c.654G>C | synonymous_variant | 1.0 |
| pepQ | 2859771 | c.648T>C | synonymous_variant | 1.0 |
| pepQ | 2860404 | p.Gln5His | missense_variant | 1.0 |
| pepQ | 2860420 | c.-2T>G | upstream_gene_variant | 1.0 |
| pepQ | 2860421 | c.-3G>A | upstream_gene_variant | 1.0 |
| pepQ | 2860423 | c.-5G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860424 | c.-6A>G | 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 | 2860448 | c.-30C>G | upstream_gene_variant | 1.0 |
| pepQ | 2860476 | c.-58A>G | upstream_gene_variant | 1.0 |
| pepQ | 2860479 | c.-63_-61delCGCinsTAT | upstream_gene_variant | 1.0 |
| pepQ | 2860482 | c.-64A>G | upstream_gene_variant | 1.0 |
| pepQ | 2860499 | c.-81C>G | upstream_gene_variant | 1.0 |
| pepQ | 2860503 | c.-85G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3064539 | c.1653T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064560 | c.1632C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064563 | c.1629A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064566 | c.1626G>C | synonymous_variant | 0.67 |
| Rv2752c | 3064776 | c.1416T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064779 | c.1413C>T | synonymous_variant | 1.0 |
| Rv2752c | 3064787 | p.Ser469Ala | missense_variant | 1.0 |
| Rv2752c | 3064790 | c.1402T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064791 | c.1401T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064794 | c.1398C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064800 | c.1392G>A | synonymous_variant | 1.0 |
| Rv2752c | 3064803 | c.1389C>T | synonymous_variant | 0.88 |
| Rv2752c | 3064809 | c.1383C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064815 | c.1377T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064832 | p.Ala454Thr | missense_variant | 0.91 |
| Rv2752c | 3064838 | c.1354T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064839 | c.1353C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064872 | c.1320T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064877 | p.Ser439Ala | missense_variant | 1.0 |
| Rv2752c | 3064881 | c.1311T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064887 | c.1305A>G | synonymous_variant | 0.95 |
| Rv2752c | 3064890 | c.1302C>A | synonymous_variant | 1.0 |
| Rv2752c | 3064893 | p.Ala433Gly | missense_variant | 1.0 |
| Rv2752c | 3064896 | c.1296T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064914 | c.1278T>G | synonymous_variant | 1.0 |
| Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064943 | p.Gln417Glu | missense_variant | 1.0 |
| Rv2752c | 3064950 | c.1242C>T | synonymous_variant | 1.0 |
| Rv2752c | 3064956 | c.1236T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064965 | c.1227G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064968 | c.1224G>A | synonymous_variant | 1.0 |
| Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065016 | c.1176C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065022 | c.1170G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065732 | c.460T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065739 | c.453G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065743 | p.Thr150Ile | missense_variant | 1.0 |
| Rv2752c | 3065748 | c.444T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065775 | c.417T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065785 | c.404_406delGGC | disruptive_inframe_deletion | 1.0 |
| Rv2752c | 3065795 | c.396_397insCGC | conservative_inframe_insertion | 1.0 |
| Rv2752c | 3065799 | c.393C>A | synonymous_variant | 1.0 |
| Rv2752c | 3065806 | p.Arg129Ala | missense_variant | 1.0 |
| Rv2752c | 3065816 | p.Val126Ile | missense_variant | 1.0 |
| Rv2752c | 3065856 | c.336T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065862 | c.330T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065867 | c.325T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065874 | c.318G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065877 | c.315G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065889 | c.303G>C | synonymous_variant | 0.96 |
| Rv2752c | 3065892 | c.300C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065901 | c.291A>T | synonymous_variant | 1.0 |
| Rv2752c | 3065916 | c.276T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065922 | c.270T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 1.0 |
| Rv2752c | 3065957 | c.235T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065972 | p.Ile74Val | missense_variant | 1.0 |
| Rv2752c | 3065979 | c.213T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065997 | c.195C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066002 | p.Met64Leu | missense_variant | 1.0 |
| Rv2752c | 3066003 | c.189C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066018 | c.174T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066024 | p.Gly56Ala | missense_variant | 1.0 |
| Rv2752c | 3066027 | c.165C>G | 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>C | synonymous_variant | 1.0 |
| Rv2752c | 3066066 | c.126T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066071 | c.121T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066074 | c.118C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066087 | c.105A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066096 | c.96G>C | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 1.0 |
| Rv2752c | 3066129 | c.63G>C | synonymous_variant | 1.0 |
| Rv2752c | 3066146 | c.46T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066154 | p.Ser13Val | missense_variant | 1.0 |
| Rv2752c | 3066174 | c.18C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066329 | c.-138C>T | upstream_gene_variant | 1.0 |
| Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066336 | c.-145C>G | upstream_gene_variant | 1.0 |
| Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066357 | c.-166G>A | upstream_gene_variant | 1.0 |
| Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066363 | c.-172G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066381 | c.-190C>T | upstream_gene_variant | 1.0 |
| Rv2752c | 3066390 | c.-199C>A | upstream_gene_variant | 1.0 |
| thyX | 3067277 | c.669C>G | synonymous_variant | 1.0 |
| thyX | 3067280 | p.Val222Ala | missense_variant | 1.0 |
| thyX | 3067284 | p.Ala221Asp | missense_variant | 1.0 |
| thyX | 3067287 | p.Ala220Val | missense_variant | 1.0 |
| thyX | 3067304 | p.Glu214Ala | missense_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067337 | p.His203Gln | missense_variant | 1.0 |
| thyX | 3067347 | p.Ala200Gly | missense_variant | 1.0 |
| thyX | 3067355 | c.591A>G | synonymous_variant | 1.0 |
| thyX | 3067358 | c.588C>T | synonymous_variant | 1.0 |
| thyX | 3067364 | c.582C>T | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 1.0 |
| thyX | 3067427 | c.519G>C | synonymous_variant | 1.0 |
| thyX | 3067433 | c.513C>A | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067442 | c.504C>G | synonymous_variant | 1.0 |
| thyX | 3067454 | c.492C>A | synonymous_variant | 1.0 |
| thyX | 3067475 | p.Gln157Glu | missense_variant | 1.0 |
| thyX | 3067500 | p.Lys149Arg | missense_variant | 1.0 |
| thyX | 3067503 | p.Ala148Gly | missense_variant | 1.0 |
| thyX | 3067515 | p.Ser144Thr | missense_variant | 1.0 |
| thyX | 3067526 | c.420C>G | synonymous_variant | 1.0 |
| thyX | 3067530 | p.Ala139Ser | missense_variant | 1.0 |
| thyX | 3067535 | c.411C>T | synonymous_variant | 1.0 |
| thyX | 3067595 | c.351C>G | synonymous_variant | 0.8 |
| thyX | 3067602 | p.Arg115Gln | missense_variant | 0.8 |
| thyX | 3067607 | p.Asp113Gln | missense_variant | 0.8 |
| thyX | 3067611 | p.Lys112Arg | missense_variant | 0.8 |
| thyX | 3067616 | c.330C>G | synonymous_variant | 0.83 |
| thyX | 3067619 | c.327A>G | synonymous_variant | 0.75 |
| thyX | 3067631 | c.315C>G | synonymous_variant | 0.8 |
| thyX | 3067634 | c.312C>G | synonymous_variant | 0.8 |
| thyX | 3067637 | c.309G>A | synonymous_variant | 0.8 |
| thyX | 3067640 | c.306G>A | synonymous_variant | 0.82 |
| thyX | 3067643 | c.303C>T | synonymous_variant | 0.85 |
| thyX | 3067652 | c.294T>C | synonymous_variant | 0.94 |
| thyX | 3067658 | c.288C>T | synonymous_variant | 0.95 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 0.95 |
| thyX | 3067676 | c.270C>T | synonymous_variant | 0.96 |
| thyX | 3067685 | c.261A>G | synonymous_variant | 0.96 |
| thyX | 3067691 | c.255C>T | synonymous_variant | 0.96 |
| thyX | 3067694 | c.252G>C | synonymous_variant | 0.97 |
| thyX | 3067716 | p.Ser77Thr | missense_variant | 0.97 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 0.97 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 0.97 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 0.97 |
| thyX | 3067738 | p.Phe70Leu | missense_variant | 1.0 |
| thyX | 3067742 | c.204A>G | synonymous_variant | 1.0 |
| thyX | 3067756 | p.Ile64Val | missense_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 1.0 |
| thyX | 3067766 | c.180C>T | synonymous_variant | 1.0 |
| thyX | 3067781 | c.165C>G | synonymous_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067814 | c.132T>C | synonymous_variant | 1.0 |
| thyX | 3067820 | c.126C>G | synonymous_variant | 1.0 |
| thyX | 3067841 | c.105G>C | synonymous_variant | 1.0 |
| thyX | 3067844 | c.102G>A | synonymous_variant | 1.0 |
| thyX | 3067847 | p.Pro33Gln | missense_variant | 1.0 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 1.0 |
| thyX | 3067859 | c.87C>T | synonymous_variant | 1.0 |
| thyX | 3067868 | p.Thr26Ser | missense_variant | 1.0 |
| thyX | 3067874 | c.72C>G | synonymous_variant | 1.0 |
| thyX | 3067880 | c.66C>T | synonymous_variant | 1.0 |
| thyX | 3067883 | c.63C>G | synonymous_variant | 1.0 |
| thyX | 3067886 | c.60A>G | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 1.0 |
| thyX | 3067892 | p.Leu18Phe | missense_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyX | 3067901 | c.45C>A | synonymous_variant | 1.0 |
| thyX | 3067922 | c.24C>T | synonymous_variant | 1.0 |
| thyA | 3073794 | c.678A>G | synonymous_variant | 1.0 |
| thyA | 3073800 | c.672G>A | synonymous_variant | 1.0 |
| thyA | 3073803 | c.669G>A | synonymous_variant | 1.0 |
| thyA | 3073818 | c.654G>A | synonymous_variant | 1.0 |
| thyA | 3073821 | c.651G>T | synonymous_variant | 1.0 |
| thyA | 3073824 | c.648A>G | synonymous_variant | 1.0 |
| thyA | 3073827 | c.645A>G | synonymous_variant | 1.0 |
| thyA | 3073839 | c.633T>C | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>T | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073881 | c.591C>T | synonymous_variant | 1.0 |
| thyA | 3073887 | p.Ser195Thr | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073893 | c.579C>T | synonymous_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>G | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
| thyA | 3073962 | c.510G>C | synonymous_variant | 1.0 |
| thyA | 3073980 | c.492C>T | synonymous_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074010 | c.462C>G | synonymous_variant | 1.0 |
| thyA | 3074013 | c.459C>T | synonymous_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| thyA | 3074079 | c.393G>C | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074103 | c.369C>G | synonymous_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| thyA | 3074117 | c.355C>T | synonymous_variant | 1.0 |
| thyA | 3074121 | p.Asp117Glu | missense_variant | 1.0 |
| thyA | 3074134 | c.337_338delAGinsTC | synonymous_variant | 1.0 |
| thyA | 3074147 | p.Ile109Val | missense_variant | 1.0 |
| thyA | 3074154 | c.318T>C | synonymous_variant | 1.0 |
| thyA | 3074160 | c.312A>G | synonymous_variant | 1.0 |
| thyA | 3074165 | p.Ala103Thr | missense_variant | 1.0 |
| thyA | 3074166 | c.306G>A | synonymous_variant | 1.0 |
| thyA | 3074175 | c.297A>G | synonymous_variant | 1.0 |
| thyA | 3074268 | c.204T>C | synonymous_variant | 1.0 |
| thyA | 3074274 | c.198T>C | synonymous_variant | 1.0 |
| thyA | 3074305 | p.Ala56Val | missense_variant | 1.0 |
| thyA | 3074307 | c.165A>G | synonymous_variant | 1.0 |
| thyA | 3074313 | c.159A>G | synonymous_variant | 1.0 |
| thyA | 3074316 | 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 | 3074334 | c.138T>C | synonymous_variant | 1.0 |
| thyA | 3074339 | p.Leu45Ile | missense_variant | 1.0 |
| thyA | 3074360 | c.112T>C | synonymous_variant | 1.0 |
| thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
| thyA | 3074376 | p.Gln32His | missense_variant | 1.0 |
| thyA | 3074409 | c.63C>A | synonymous_variant | 1.0 |
| thyA | 3074417 | p.Ser19Ala | missense_variant | 1.0 |
| thyA | 3074427 | c.45T>C | synonymous_variant | 1.0 |
| ald | 3087479 | c.660A>C | synonymous_variant | 1.0 |
| ald | 3087487 | p.Tyr223Phe | missense_variant | 1.0 |
| ald | 3087499 | p.Gly227Asp | missense_variant | 1.0 |
| ald | 3087527 | c.708T>C | synonymous_variant | 1.0 |
| ald | 3087530 | c.711G>A | synonymous_variant | 1.0 |
| ald | 3087626 | c.807C>A | synonymous_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 | 3087655 | p.Arg279His | missense_variant | 1.0 |
| ald | 3087666 | p.Tyr283His | missense_variant | 1.0 |
| ald | 3087672 | p.His285Asp | missense_variant | 1.0 |
| ald | 3087696 | p.Thr293Ala | missense_variant | 1.0 |
| ald | 3087699 | p.Leu294Met | missense_variant | 1.0 |
| ald | 3087704 | c.885T>C | synonymous_variant | 1.0 |
| ald | 3087714 | p.Ala299Thr | missense_variant | 0.95 |
| ald | 3087725 | c.906C>G | synonymous_variant | 1.0 |
| ald | 3087728 | c.909C>T | synonymous_variant | 1.0 |
| ald | 3087740 | c.921G>A | synonymous_variant | 1.0 |
| ald | 3087749 | c.930C>G | synonymous_variant | 1.0 |
| ald | 3087751 | p.Tyr311Phe | missense_variant | 1.0 |
| ald | 3087756 | c.937C>T | synonymous_variant | 1.0 |
| ald | 3087770 | c.951G>C | synonymous_variant | 1.0 |
| fbiD | 3339171 | c.54C>G | synonymous_variant | 1.0 |
| fbiD | 3339172 | c.55_57delTTGinsCTC | synonymous_variant | 1.0 |
| fbiD | 3339180 | c.63G>C | synonymous_variant | 1.0 |
| fbiD | 3339186 | c.69A>G | synonymous_variant | 1.0 |
| fbiD | 3339198 | c.81C>G | synonymous_variant | 1.0 |
| fbiD | 3339213 | c.96G>A | synonymous_variant | 1.0 |
| fbiD | 3339219 | c.102T>C | synonymous_variant | 1.0 |
| fbiD | 3339222 | c.105C>G | synonymous_variant | 1.0 |
| fbiD | 3339225 | c.108G>A | synonymous_variant | 1.0 |
| fbiD | 3339227 | p.Asn37Thr | missense_variant | 1.0 |
| fbiD | 3339235 | c.118C>T | synonymous_variant | 1.0 |
| fprA | 3473812 | c.-195G>A | upstream_gene_variant | 1.0 |
| fprA | 3473815 | c.-192G>C | upstream_gene_variant | 1.0 |
| fprA | 3473843 | c.-164C>G | upstream_gene_variant | 1.0 |
| fprA | 3473848 | c.-159_-157delCAAinsGAG | upstream_gene_variant | 1.0 |
| fprA | 3473866 | c.-141T>C | upstream_gene_variant | 1.0 |
| fprA | 3473869 | c.-138A>G | upstream_gene_variant | 1.0 |
| fprA | 3473872 | c.-135G>A | upstream_gene_variant | 1.0 |
| fprA | 3473878 | c.-129G>T | upstream_gene_variant | 1.0 |
| fprA | 3474130 | c.124T>C | synonymous_variant | 1.0 |
| fprA | 3474135 | c.129G>C | synonymous_variant | 1.0 |
| fprA | 3474138 | c.132T>G | synonymous_variant | 1.0 |
| fprA | 3474141 | c.135C>G | synonymous_variant | 1.0 |
| fprA | 3474153 | c.147G>C | synonymous_variant | 1.0 |
| fprA | 3474162 | c.156G>C | synonymous_variant | 1.0 |
| fprA | 3474168 | c.162G>A | synonymous_variant | 1.0 |
| fprA | 3474171 | c.165G>C | synonymous_variant | 1.0 |
| fprA | 3474174 | c.168T>C | synonymous_variant | 1.0 |
| fprA | 3474180 | c.174C>G | synonymous_variant | 1.0 |
| fprA | 3474200 | p.Lys65Arg | missense_variant | 1.0 |
| fprA | 3474204 | c.198A>G | synonymous_variant | 1.0 |
| fprA | 3474213 | c.207G>A | synonymous_variant | 1.0 |
| fprA | 3474216 | c.210G>C | synonymous_variant | 1.0 |
| fprA | 3474217 | p.Ala71Ser | missense_variant | 1.0 |
| fprA | 3474237 | c.231C>G | synonymous_variant | 1.0 |
| fprA | 3474303 | c.297C>G | synonymous_variant | 1.0 |
| fprA | 3474312 | c.306C>T | synonymous_variant | 1.0 |
| fprA | 3474315 | c.309C>G | synonymous_variant | 1.0 |
| fprA | 3474316 | p.Val104Ile | missense_variant | 1.0 |
| fprA | 3474327 | c.321G>A | synonymous_variant | 1.0 |
| fprA | 3474336 | c.330C>G | synonymous_variant | 1.0 |
| fprA | 3474337 | p.Met111Ala | missense_variant | 1.0 |
| fprA | 3474340 | c.334T>C | synonymous_variant | 1.0 |
| fprA | 3474348 | c.342C>T | synonymous_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 | 3474378 | c.372C>G | synonymous_variant | 1.0 |
| fprA | 3474381 | c.375C>G | synonymous_variant | 1.0 |
| fprA | 3474699 | p.Asp231Glu | missense_variant | 0.71 |
| fprA | 3474705 | c.699T>C | synonymous_variant | 0.86 |
| fprA | 3474707 | p.Thr234Ser | missense_variant | 0.87 |
| fprA | 3474714 | p.Glu236Asp | missense_variant | 0.89 |
| fprA | 3474722 | p.Ala239Val | missense_variant | 1.0 |
| fprA | 3474765 | c.759T>C | synonymous_variant | 0.97 |
| fprA | 3474771 | c.765T>C | synonymous_variant | 0.97 |
| fprA | 3474777 | p.Asp257Glu | missense_variant | 0.97 |
| fprA | 3474783 | c.777A>G | synonymous_variant | 0.97 |
| fprA | 3474792 | c.786G>T | synonymous_variant | 0.97 |
| fprA | 3474801 | c.795C>T | synonymous_variant | 0.95 |
| fprA | 3474804 | c.798C>A | synonymous_variant | 0.93 |
| fprA | 3474807 | p.Met267Ile | missense_variant | 0.93 |
| fprA | 3474825 | c.819C>A | synonymous_variant | 1.0 |
| fprA | 3474828 | c.822T>C | synonymous_variant | 1.0 |
| fprA | 3474836 | p.Glu277Ala | missense_variant | 1.0 |
| fprA | 3475061 | p.Pro352Arg | missense_variant | 1.0 |
| fprA | 3475068 | c.1062A>G | synonymous_variant | 1.0 |
| fprA | 3475080 | c.1074G>C | synonymous_variant | 1.0 |
| fprA | 3475113 | c.1107G>C | synonymous_variant | 1.0 |
| fprA | 3475125 | c.1119G>A | synonymous_variant | 0.91 |
| fprA | 3475129 | p.Ala375Ser | missense_variant | 0.9 |
| fprA | 3475134 | c.1128A>G | synonymous_variant | 0.88 |
| fprA | 3475150 | c.1144T>C | synonymous_variant | 0.75 |
| Rv3236c | 3612829 | c.288T>C | synonymous_variant | 1.0 |
| Rv3236c | 3612835 | p.Gly94Ala | missense_variant | 1.0 |
| Rv3236c | 3612844 | c.273G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612855 | p.His88Tyr | missense_variant | 1.0 |
| Rv3236c | 3612862 | c.255T>C | synonymous_variant | 1.0 |
| Rv3236c | 3612874 | c.243G>A | synonymous_variant | 1.0 |
| Rv3236c | 3612879 | p.Thr80Pro | missense_variant | 1.0 |
| Rv3236c | 3612880 | c.237G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612883 | c.234T>C | synonymous_variant | 1.0 |
| Rv3236c | 3612886 | c.231T>C | synonymous_variant | 1.0 |
| Rv3236c | 3612895 | c.222T>C | synonymous_variant | 1.0 |
| fbiA | 3640536 | c.-7C>G | upstream_gene_variant | 0.8 |
| fbiB | 3640554 | c.-981C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640562 | p.Ala7Val | missense_variant | 1.0 |
| fbiB | 3640566 | c.-969T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640569 | c.-966A>T | upstream_gene_variant | 1.0 |
| fbiB | 3640581 | c.-954C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640587 | c.-948C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640590 | c.-945G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640596 | c.-939G>T | upstream_gene_variant | 1.0 |
| fbiB | 3640599 | c.-936C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640611 | c.-924C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640614 | c.-921C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640660 | p.Gln40Glu | missense_variant | 1.0 |
| fbiA | 3640667 | p.Ser42Thr | missense_variant | 1.0 |
| fbiB | 3640671 | c.-864T>G | upstream_gene_variant | 0.8 |
| fbiA | 3640672 | p.Val44Ile | missense_variant | 0.8 |
| fbiA | 3640681 | p.Val47Ile | missense_variant | 0.88 |
| fbiA | 3640701 | p.Ile53Met | missense_variant | 0.94 |
| fbiB | 3640707 | c.-828G>C | upstream_gene_variant | 0.95 |
| fbiB | 3640713 | c.-822T>C | upstream_gene_variant | 0.96 |
| fbiB | 3640725 | c.-810T>C | upstream_gene_variant | 0.97 |
| fbiB | 3640728 | c.-807G>A | upstream_gene_variant | 0.97 |
| fbiB | 3640758 | c.-777G>C | upstream_gene_variant | 0.98 |
| fbiB | 3640761 | c.-774G>C | upstream_gene_variant | 0.98 |
| fbiB | 3640767 | c.-768C>G | upstream_gene_variant | 0.98 |
| fbiA | 3640768 | p.Gln76Glu | missense_variant | 0.98 |
| fbiB | 3640782 | c.-753C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640785 | p.Gln81His | missense_variant | 1.0 |
| fbiB | 3640788 | c.-747T>G | upstream_gene_variant | 1.0 |
| fbiB | 3640797 | c.-738T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640808 | p.Met89Lys | missense_variant | 1.0 |
| fbiA | 3640810 | p.Gln90Glu | missense_variant | 0.97 |
| fbiB | 3640821 | c.-714G>T | upstream_gene_variant | 1.0 |
| fbiB | 3640824 | c.-711C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640848 | c.-687C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640849 | p.Glu103Gln | missense_variant | 1.0 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640861 | p.Arg107Lys | missense_variant | 1.0 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640889 | p.Thr116Ser | missense_variant | 1.0 |
| fbiA | 3640901 | p.Gln120Arg | missense_variant | 1.0 |
| fbiB | 3640908 | c.-627C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640989 | c.-546T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641004 | c.-531A>C | upstream_gene_variant | 1.0 |
| fbiB | 3641007 | c.-528G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641016 | c.-519C>T | upstream_gene_variant | 1.0 |
| fbiB | 3641019 | c.-516G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641028 | c.-507A>G | upstream_gene_variant | 1.0 |
| fbiA | 3641031 | c.491_492delGC | frameshift_variant | 1.0 |
| fbiA | 3641036 | c.494_495insCG | frameshift_variant | 1.0 |
| fbiB | 3641046 | c.-489T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641049 | c.-486T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641052 | c.-483G>A | upstream_gene_variant | 1.0 |
| fbiA | 3641068 | p.Tyr176His | missense_variant | 1.0 |
| fbiB | 3641073 | c.-462T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641993 | c.459A>C | synonymous_variant | 1.0 |
| fbiB | 3641999 | c.465C>T | synonymous_variant | 1.0 |
| fbiB | 3642020 | c.486T>C | synonymous_variant | 1.0 |
| fbiB | 3642023 | c.489C>G | synonymous_variant | 1.0 |
| fbiB | 3642026 | c.492A>C | synonymous_variant | 1.0 |
| fbiB | 3642035 | c.501T>G | synonymous_variant | 1.0 |
| fbiB | 3642057 | p.Asn175Gly | missense_variant | 1.0 |
| fbiB | 3642068 | c.534T>C | synonymous_variant | 1.0 |
| fbiB | 3642070 | p.Val179Ala | missense_variant | 1.0 |
| fbiB | 3642073 | p.Arg180Leu | missense_variant | 1.0 |
| fbiB | 3642078 | p.Pro182Ala | missense_variant | 1.0 |
| fbiB | 3642081 | p.Tyr183His | missense_variant | 1.0 |
| fbiB | 3642089 | c.555T>C | synonymous_variant | 1.0 |
| fbiB | 3642098 | c.564G>T | synonymous_variant | 1.0 |
| fbiB | 3642113 | c.579A>C | synonymous_variant | 1.0 |
| fbiB | 3642140 | c.606C>G | synonymous_variant | 1.0 |
| fbiB | 3642143 | c.609C>T | synonymous_variant | 1.0 |
| fbiB | 3642144 | c.610T>C | synonymous_variant | 1.0 |
| fbiB | 3642152 | c.618A>G | synonymous_variant | 1.0 |
| fbiB | 3642158 | c.624A>G | synonymous_variant | 1.0 |
| fbiB | 3642542 | c.1008A>G | synonymous_variant | 1.0 |
| fbiB | 3642578 | c.1044C>G | synonymous_variant | 1.0 |
| fbiB | 3642581 | c.1047A>C | synonymous_variant | 1.0 |
| fbiB | 3642587 | p.Met351Ile | missense_variant | 1.0 |
| fbiB | 3642588 | p.Leu352Met | missense_variant | 1.0 |
| fbiB | 3642602 | c.1068A>C | synonymous_variant | 1.0 |
| fbiB | 3642605 | c.1071A>G | synonymous_variant | 1.0 |
| fbiB | 3642611 | c.1077C>T | synonymous_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 | 3642632 | c.1098C>A | synonymous_variant | 1.0 |
| fbiB | 3642656 | c.1122G>C | synonymous_variant | 1.0 |
| fbiB | 3642662 | c.1128C>G | synonymous_variant | 1.0 |
| fbiB | 3642692 | c.1158C>G | synonymous_variant | 1.0 |
| fbiB | 3642701 | c.1167C>A | synonymous_variant | 1.0 |
| fbiB | 3642707 | c.1173C>T | synonymous_variant | 1.0 |
| fbiB | 3642710 | c.1176G>A | synonymous_variant | 1.0 |
| fbiB | 3642711 | p.Leu393Val | missense_variant | 1.0 |
| fbiB | 3642719 | c.1185T>C | synonymous_variant | 1.0 |
| fbiB | 3642743 | c.1209T>C | synonymous_variant | 1.0 |
| fbiB | 3642749 | c.1215T>C | synonymous_variant | 1.0 |
| fbiB | 3642752 | c.1218C>T | synonymous_variant | 1.0 |
| fbiB | 3642772 | p.Asp413Gly | missense_variant | 1.0 |
| fbiB | 3642779 | c.1245A>T | synonymous_variant | 1.0 |
| fbiB | 3642781 | p.Val416Gly | missense_variant | 1.0 |
| fbiB | 3642785 | c.1251C>T | synonymous_variant | 1.0 |
| fbiB | 3642791 | c.1257G>A | synonymous_variant | 1.0 |
| alr | 3840926 | c.495T>C | synonymous_variant | 1.0 |
| alr | 3840937 | c.484C>T | synonymous_variant | 1.0 |
| alr | 3840938 | c.483G>A | synonymous_variant | 1.0 |
| alr | 3840944 | c.477T>C | synonymous_variant | 1.0 |
| alr | 3840947 | c.474G>C | synonymous_variant | 1.0 |
| alr | 3840972 | p.Arg150Glu | missense_variant | 1.0 |
| alr | 3840974 | c.447C>T | synonymous_variant | 1.0 |
| alr | 3840980 | c.441G>C | synonymous_variant | 1.0 |
| alr | 3840994 | p.His143Asp | missense_variant | 1.0 |
| alr | 3840995 | c.424_426delTTGinsCTC | synonymous_variant | 1.0 |
| alr | 3841001 | p.Glu140Asp | missense_variant | 1.0 |
| alr | 3841013 | c.408C>T | synonymous_variant | 1.0 |
| alr | 3841018 | p.Leu135Val | missense_variant | 1.0 |
| alr | 3841033 | p.Val130Ile | missense_variant | 1.0 |
| alr | 3841037 | p.Val128Ile | missense_variant | 1.0 |
| alr | 3841041 | p.Asp127Gly | missense_variant | 1.0 |
| alr | 3841047 | p.Leu125Thr | missense_variant | 1.0 |
| alr | 3841051 | c.370C>T | synonymous_variant | 1.0 |
| alr | 3841055 | c.366C>G | synonymous_variant | 1.0 |
| alr | 3841059 | p.Gly121Ala | missense_variant | 1.0 |
| alr | 3841068 | p.Ile118Thr | missense_variant | 1.0 |
| alr | 3841077 | p.Pro115Arg | missense_variant | 1.0 |
| alr | 3841079 | c.342T>C | synonymous_variant | 1.0 |
| alr | 3841088 | c.333C>G | synonymous_variant | 1.0 |
| alr | 3841106 | c.315T>C | synonymous_variant | 1.0 |
| alr | 3841112 | c.309T>C | synonymous_variant | 1.0 |
| alr | 3841115 | c.306T>C | synonymous_variant | 1.0 |
| alr | 3841118 | c.303C>G | synonymous_variant | 1.0 |
| alr | 3841123 | c.298C>T | synonymous_variant | 1.0 |
| alr | 3841127 | c.294A>G | synonymous_variant | 1.0 |
| alr | 3841151 | c.270C>T | synonymous_variant | 1.0 |
| alr | 3841163 | c.258G>C | synonymous_variant | 1.0 |
| rpoA | 3877494 | p.Glu338Asp | missense_variant | 1.0 |
| rpoA | 3877503 | p.Ala335Gly | missense_variant | 1.0 |
| rpoA | 3877509 | p.Glu333Asp | missense_variant | 1.0 |
| rpoA | 3877513 | p.Thr332Ser | missense_variant | 1.0 |
| rpoA | 3877515 | c.993G>C | synonymous_variant | 1.0 |
| rpoA | 3877542 | c.966C>T | synonymous_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877569 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877596 | c.912G>C | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877679 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877689 | c.819C>T | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 0.98 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 0.98 |
| rpoA | 3877731 | c.777G>C | synonymous_variant | 0.98 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 0.98 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 0.99 |
| 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 | 3877794 | c.714G>C | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877827 | c.681C>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>G | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877863 | c.645G>T | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877872 | c.636C>T | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
| rpoA | 3877881 | c.627G>T | synonymous_variant | 1.0 |
| rpoA | 3877893 | c.615C>G | synonymous_variant | 1.0 |
| rpoA | 3877899 | p.Ser203Thr | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877908 | p.Asn200Ser | missense_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 0.95 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 0.98 |
| rpoA | 3877986 | c.522G>C | synonymous_variant | 0.98 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 0.98 |
| rpoA | 3877992 | c.516C>G | synonymous_variant | 0.98 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 0.98 |
| rpoA | 3878016 | c.492C>T | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878025 | c.483C>T | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878040 | c.468T>C | synonymous_variant | 1.0 |
| rpoA | 3878046 | c.462T>G | synonymous_variant | 1.0 |
| rpoA | 3878050 | p.Arg153Lys | missense_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878067 | c.441C>G | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878079 | c.429C>G | synonymous_variant | 0.97 |
| rpoA | 3878094 | c.414C>G | synonymous_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
| rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
| rpoA | 3878109 | c.399G>A | synonymous_variant | 1.0 |
| rpoA | 3878115 | c.393G>A | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
| rpoA | 3878133 | c.375C>T | synonymous_variant | 1.0 |
| rpoA | 3878143 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878145 | c.363C>T | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>T | synonymous_variant | 1.0 |
| rpoA | 3878184 | c.324C>T | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878199 | c.309T>C | synonymous_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878241 | c.267G>A | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878268 | c.240C>G | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.99 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 0.99 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 0.99 |
| rpoA | 3878304 | c.204G>C | synonymous_variant | 0.99 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 0.97 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 0.99 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 0.99 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 0.99 |
| rpoA | 3878358 | c.150C>G | synonymous_variant | 0.99 |
| rpoA | 3878361 | c.147G>A | synonymous_variant | 0.98 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 0.98 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 0.97 |
| rpoA | 3878382 | c.126G>C | synonymous_variant | 0.98 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 0.98 |
| rpoA | 3878391 | c.117T>C | synonymous_variant | 0.98 |
| rpoA | 3878406 | c.102G>T | synonymous_variant | 0.95 |
| rpoA | 3878409 | c.99C>G | synonymous_variant | 0.98 |
| rpoA | 3878424 | c.84G>A | synonymous_variant | 0.97 |
| rpoA | 3878427 | c.81G>A | synonymous_variant | 0.93 |
| rpoA | 3878442 | c.66G>C | synonymous_variant | 0.94 |
| rpoA | 3878451 | c.57C>G | synonymous_variant | 0.93 |
| rpoA | 3878454 | c.54A>G | synonymous_variant | 0.93 |
| rpoA | 3878458 | p.Asn17Thr | missense_variant | 0.93 |
| rpoA | 3878460 | c.48C>T | synonymous_variant | 0.93 |
| rpoA | 3878468 | p.Leu14Val | missense_variant | 0.93 |
| rpoA | 3878470 | p.Val13Ala | missense_variant | 0.93 |
| rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
| rpoA | 3878475 | c.33G>A | synonymous_variant | 1.0 |
| rpoA | 3878484 | c.24C>A | synonymous_variant | 1.0 |
| rpoA | 3878490 | c.18C>A | synonymous_variant | 1.0 |
| rpoA | 3878518 | c.-12delA | upstream_gene_variant | 1.0 |
| rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 1.0 |
| rpoA | 3878694 | c.-187A>G | 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 | 3986646 | c.-198_-196delCTCinsTTG | upstream_gene_variant | 1.0 |
| ddn | 3986654 | c.-190C>T | upstream_gene_variant | 1.0 |
| ddn | 3986655 | c.-189A>T | upstream_gene_variant | 1.0 |
| ddn | 3986660 | c.-184C>T | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-175delCTCinsACG | 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 |
| clpC1 | 4038197 | c.2508A>T | synonymous_variant | 1.0 |
| clpC1 | 4038200 | c.2505T>C | synonymous_variant | 1.0 |
| clpC1 | 4038212 | c.2493T>C | synonymous_variant | 1.0 |
| clpC1 | 4038224 | c.2481G>C | synonymous_variant | 1.0 |
| clpC1 | 4038226 | c.2478_2479insGCCGAG | conservative_inframe_insertion | 1.0 |
| clpC1 | 4038239 | c.2466T>G | synonymous_variant | 1.0 |
| clpC1 | 4038248 | c.2457C>G | synonymous_variant | 1.0 |
| clpC1 | 4038255 | p.Val817Lys | missense_variant | 1.0 |
| clpC1 | 4038271 | p.Pro812Ala | missense_variant | 1.0 |
| clpC1 | 4038272 | c.2433T>C | synonymous_variant | 1.0 |
| clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
| clpC1 | 4038308 | p.Val799Ile | missense_variant | 1.0 |
| clpC1 | 4038314 | c.2391T>C | synonymous_variant | 1.0 |
| clpC1 | 4038320 | c.2385G>T | synonymous_variant | 1.0 |
| clpC1 | 4038338 | c.2367C>T | synonymous_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 | 4038377 | c.2328C>G | synonymous_variant | 0.98 |
| clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
| clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
| clpC1 | 4038407 | c.2298G>C | synonymous_variant | 1.0 |
| clpC1 | 4038410 | c.2295C>T | synonymous_variant | 1.0 |
| clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
| clpC1 | 4038428 | c.2277G>C | synonymous_variant | 1.0 |
| clpC1 | 4038436 | p.Ala757Ser | missense_variant | 1.0 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
| clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
| clpC1 | 4038485 | p.Gly740Lys | missense_variant | 1.0 |
| clpC1 | 4038488 | p.Ala739Glu | missense_variant | 1.0 |
| clpC1 | 4038498 | p.Ser736Asn | missense_variant | 1.0 |
| clpC1 | 4038509 | p.Asp732Glu | missense_variant | 1.0 |
| clpC1 | 4038530 | c.2175G>A | synonymous_variant | 1.0 |
| clpC1 | 4038536 | c.2169C>T | synonymous_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038644 | p.Glu687Ala | missense_variant | 1.0 |
| clpC1 | 4038653 | c.2052C>T | synonymous_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 | 4038679 | p.Pro676Ala | missense_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038692 | p.Ser671Ala | missense_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>G | synonymous_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038749 | c.1956C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>A | synonymous_variant | 1.0 |
| clpC1 | 4038818 | c.1887G>A | synonymous_variant | 1.0 |
| clpC1 | 4038827 | c.1878G>A | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>A | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038884 | c.1821C>T | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.97 |
| clpC1 | 4038914 | c.1791G>A | 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 | 4039001 | p.Asn568Glu | missense_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039034 | c.1671C>G | synonymous_variant | 1.0 |
| clpC1 | 4039037 | c.1668T>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>G | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>T | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039124 | c.1581C>G | synonymous_variant | 1.0 |
| clpC1 | 4039127 | p.Lys526Asn | missense_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039163 | p.Leu514Ile | missense_variant | 1.0 |
| clpC1 | 4039169 | c.1536A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039189 | c.1516C>A | synonymous_variant | 1.0 |
| clpC1 | 4039271 | c.1434G>A | synonymous_variant | 0.98 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.98 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.97 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.97 |
| clpC1 | 4039295 | c.1410A>T | synonymous_variant | 0.96 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.96 |
| clpC1 | 4039304 | c.1401G>A | synonymous_variant | 0.96 |
| clpC1 | 4039313 | c.1392C>T | synonymous_variant | 0.95 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.93 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.92 |
| clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.91 |
| clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.86 |
| clpC1 | 4039336 | c.1368_1369insG | frameshift_variant | 0.83 |
| clpC1 | 4039339 | c.1365delG | frameshift_variant | 0.83 |
| clpC1 | 4039346 | c.1359G>T | synonymous_variant | 1.0 |
| clpC1 | 4039364 | c.1341C>G | synonymous_variant | 1.0 |
| clpC1 | 4039382 | c.1323C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039394 | c.1311G>C | synonymous_variant | 1.0 |
| clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
| clpC1 | 4039406 | c.1299G>C | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | c.1290G>A | synonymous_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 | 0.96 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.97 |
| clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.97 |
| clpC1 | 4039554 | p.Thr384Ser | missense_variant | 0.96 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.96 |
| clpC1 | 4039559 | c.1146C>T | synonymous_variant | 0.96 |
| clpC1 | 4039566 | p.Val380Thr | missense_variant | 0.96 |
| clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.96 |
| clpC1 | 4039574 | p.Ala377Ser | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.98 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.99 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.99 |
| clpC1 | 4039667 | c.1038G>A | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | 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 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
| clpC1 | 4039802 | c.903G>A | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039840 | c.865C>T | synonymous_variant | 0.96 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.96 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.95 |
| clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.96 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.97 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.97 |
| clpC1 | 4039922 | c.783C>T | synonymous_variant | 0.96 |
| clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.96 |
| clpC1 | 4039928 | c.775_777delAGCinsTCA | synonymous_variant | 0.95 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.95 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039943 | c.762G>A | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.98 |
| clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.98 |
| clpC1 | 4040010 | p.Ala232Asn | missense_variant | 0.98 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.98 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.98 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.98 |
| clpC1 | 4040051 | c.654C>G | synonymous_variant | 0.98 |
| clpC1 | 4040069 | c.636G>C | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>T | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.610_612delCTCinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | 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 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.75 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040252 | c.453C>T | synonymous_variant | 1.0 |
| clpC1 | 4040257 | p.Ala150Thr | missense_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040300 | c.405C>T | synonymous_variant | 1.0 |
| clpC1 | 4040309 | c.396C>T | synonymous_variant | 1.0 |
| clpC1 | 4040324 | c.381G>C | synonymous_variant | 1.0 |
| clpC1 | 4040335 | c.370C>T | synonymous_variant | 1.0 |
| clpC1 | 4040348 | c.357G>T | 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 | 4040369 | c.334_336delCTCinsTTG | 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 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040453 | c.252C>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>A | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040468 | c.237G>A | 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 | 4040546 | c.159G>A | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040567 | c.138C>A | synonymous_variant | 1.0 |
| clpC1 | 4040570 | c.135C>G | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>A | synonymous_variant | 0.98 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040588 | c.117T>C | synonymous_variant | 1.0 |
| clpC1 | 4040594 | c.111G>C | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.96 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040615 | c.90C>T | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| clpC1 | 4040662 | c.43C>T | synonymous_variant | 1.0 |
| clpC1 | 4040696 | c.9A>G | synonymous_variant | 1.0 |
| clpC1 | 4040699 | c.6C>T | synonymous_variant | 1.0 |
| clpC1 | 4040705 | c.-1G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040734 | c.-31delT | upstream_gene_variant | 1.0 |
| clpC1 | 4040745 | c.-41G>C | upstream_gene_variant | 1.0 |
| clpC1 | 4040747 | c.-43T>C | upstream_gene_variant | 1.0 |
| clpC1 | 4040750 | c.-46G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040763 | c.-59C>T | upstream_gene_variant | 1.0 |
| clpC1 | 4040777 | c.-73A>C | upstream_gene_variant | 1.0 |
| clpC1 | 4040782 | c.-78G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040783 | c.-79A>C | upstream_gene_variant | 1.0 |
| clpC1 | 4040787 | c.-83T>C | upstream_gene_variant | 1.0 |
| panD | 4044119 | c.163C>T | synonymous_variant | 1.0 |
| panD | 4044120 | c.162A>G | synonymous_variant | 1.0 |
| panD | 4044126 | c.156T>G | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044150 | c.132A>G | synonymous_variant | 1.0 |
| panD | 4044156 | c.126A>G | synonymous_variant | 1.0 |
| panD | 4044162 | c.120A>G | synonymous_variant | 1.0 |
| panD | 4044165 | c.117G>C | synonymous_variant | 1.0 |
| panD | 4044174 | c.108C>A | synonymous_variant | 1.0 |
| panD | 4044177 | c.105C>G | synonymous_variant | 1.0 |
| panD | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044192 | c.90C>T | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044225 | c.57C>T | synonymous_variant | 1.0 |
| panD | 4044228 | c.54C>G | synonymous_variant | 1.0 |
| panD | 4044237 | c.45G>C | synonymous_variant | 1.0 |
| panD | 4044240 | c.42G>C | synonymous_variant | 1.0 |
| panD | 4044243 | c.39C>A | synonymous_variant | 1.0 |
| panD | 4044246 | c.36C>G | synonymous_variant | 1.0 |
| panD | 4044264 | c.18G>C | synonymous_variant | 1.0 |
| panD | 4044270 | c.12G>A | synonymous_variant | 1.0 |
| panD | 4044287 | c.-6A>G | upstream_gene_variant | 1.0 |
| embC | 4239674 | c.-189C>T | upstream_gene_variant | 1.0 |
| embC | 4239680 | c.-183C>A | upstream_gene_variant | 1.0 |
| embC | 4239688 | c.-175A>G | upstream_gene_variant | 1.0 |
| embC | 4239696 | c.-167_-165delCATinsAAC | upstream_gene_variant | 1.0 |
| embC | 4239699 | c.-164_-162delAACinsGAG | upstream_gene_variant | 1.0 |
| embC | 4239703 | c.-160_-159delGCinsCA | upstream_gene_variant | 1.0 |
| embC | 4239710 | c.-153C>G | upstream_gene_variant | 1.0 |
| embC | 4239723 | c.-140_-138delCAGinsGAA | upstream_gene_variant | 1.0 |
| embC | 4239743 | c.-120G>A | upstream_gene_variant | 1.0 |
| embC | 4240717 | c.855T>C | synonymous_variant | 1.0 |
| embC | 4240732 | c.870C>T | synonymous_variant | 1.0 |
| embC | 4240736 | p.Ser292Ala | missense_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 0.98 |
| embC | 4240783 | c.921G>C | synonymous_variant | 0.98 |
| embC | 4240786 | c.924C>A | synonymous_variant | 0.98 |
| embC | 4240789 | c.927T>C | synonymous_variant | 0.98 |
| embC | 4240819 | c.957A>C | synonymous_variant | 0.98 |
| embC | 4240822 | c.960C>G | synonymous_variant | 0.98 |
| embC | 4240831 | c.969T>G | synonymous_variant | 0.98 |
| embC | 4240875 | p.Ser338Thr | missense_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_variant | 1.0 |
| embC | 4240880 | p.Ala340Thr | missense_variant | 1.0 |
| embC | 4240885 | c.1023T>C | synonymous_variant | 1.0 |
| embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
| embC | 4240900 | c.1038A>G | synonymous_variant | 1.0 |
| embC | 4240910 | p.Ala350Leu | missense_variant | 1.0 |
| embC | 4240921 | c.1059C>G | synonymous_variant | 1.0 |
| embC | 4240922 | p.Thr354Ala | missense_variant | 1.0 |
| embC | 4240936 | c.1074A>G | synonymous_variant | 1.0 |
| embC | 4240948 | c.1086G>A | synonymous_variant | 1.0 |
| embC | 4240954 | c.1092T>C | synonymous_variant | 1.0 |
| embC | 4240957 | c.1095C>G | synonymous_variant | 1.0 |
| embC | 4240969 | c.1107C>T | synonymous_variant | 1.0 |
| embC | 4240975 | c.1113C>G | synonymous_variant | 1.0 |
| embC | 4240981 | c.1119G>C | synonymous_variant | 1.0 |
| embC | 4240983 | p.Ser374Asn | missense_variant | 1.0 |
| embC | 4240990 | c.1128A>G | synonymous_variant | 1.0 |
| embC | 4240996 | c.1134G>C | synonymous_variant | 0.95 |
| embC | 4241005 | c.1143G>C | synonymous_variant | 1.0 |
| embC | 4241008 | c.1146G>C | synonymous_variant | 1.0 |
| embC | 4241017 | c.1155T>C | synonymous_variant | 1.0 |
| embC | 4241024 | p.Val388Phe | missense_variant | 1.0 |
| embC | 4241039 | p.Asp393Asn | missense_variant | 1.0 |
| embC | 4241047 | c.1185C>T | synonymous_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241089 | c.1227C>G | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241123 | c.1261C>A | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Val | missense_variant | 1.0 |
| embC | 4241153 | p.Ile431Val | missense_variant | 1.0 |
| embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
| embC | 4241188 | c.1326C>T | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>G | synonymous_variant | 1.0 |
| embC | 4241207 | c.1345C>T | synonymous_variant | 1.0 |
| embC | 4241215 | c.1353C>G | synonymous_variant | 1.0 |
| embC | 4241233 | c.1371G>C | synonymous_variant | 1.0 |
| embC | 4241389 | c.1527C>T | synonymous_variant | 1.0 |
| embC | 4241394 | p.Lys511Ser | missense_variant | 1.0 |
| embC | 4241407 | c.1545A>G | synonymous_variant | 1.0 |
| embC | 4241416 | c.1554C>T | synonymous_variant | 1.0 |
| embC | 4241425 | c.1563G>T | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241458 | c.1596C>T | synonymous_variant | 1.0 |
| embC | 4241470 | c.1608C>G | synonymous_variant | 1.0 |
| embC | 4241479 | c.1617C>A | synonymous_variant | 1.0 |
| embC | 4241483 | p.Val541Leu | missense_variant | 1.0 |
| embC | 4241486 | p.Leu542Val | missense_variant | 1.0 |
| embC | 4241500 | c.1638A>G | synonymous_variant | 1.0 |
| embC | 4241513 | p.Ser551Ala | missense_variant | 1.0 |
| embC | 4241518 | c.1656A>G | synonymous_variant | 1.0 |
| embC | 4241521 | c.1659T>C | synonymous_variant | 1.0 |
| embC | 4241530 | c.1668C>A | synonymous_variant | 1.0 |
| embC | 4241536 | c.1674A>G | synonymous_variant | 1.0 |
| embC | 4241539 | c.1677T>C | synonymous_variant | 1.0 |
| embC | 4241545 | c.1683T>C | synonymous_variant | 1.0 |
| embC | 4241548 | c.1686T>C | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>G | synonymous_variant | 1.0 |
| embC | 4241554 | c.1692G>C | synonymous_variant | 1.0 |
| embC | 4241556 | p.Ser565Thr | missense_variant | 1.0 |
| embC | 4241578 | c.1716G>C | synonymous_variant | 1.0 |
| embC | 4241579 | p.Ile573Val | missense_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241591 | p.Leu577Ile | missense_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embC | 4241644 | c.1782G>C | synonymous_variant | 1.0 |
| embC | 4241648 | c.1786T>C | synonymous_variant | 0.93 |
| embC | 4241656 | c.1794G>C | synonymous_variant | 1.0 |
| embC | 4241660 | c.1798C>T | synonymous_variant | 1.0 |
| embC | 4241671 | c.1809T>G | synonymous_variant | 0.75 |
| embC | 4241675 | p.Ala605Thr | missense_variant | 0.67 |
| embC | 4241723 | p.Val621Met | missense_variant | 1.0 |
| 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 |
| embC | 4242278 | p.Arg806Ser | missense_variant | 1.0 |
| embA | 4242289 | c.-944C>G | upstream_gene_variant | 1.0 |
| embC | 4242290 | p.Asn810Gly | missense_variant | 1.0 |
| embC | 4242299 | p.Gly813Arg | missense_variant | 1.0 |
| embC | 4242305 | p.Ile815Val | missense_variant | 1.0 |
| embC | 4242311 | p.Gly817Ser | missense_variant | 1.0 |
| embA | 4242319 | c.-914A>G | upstream_gene_variant | 1.0 |
| embC | 4242320 | p.Pro820Ala | missense_variant | 1.0 |
| embA | 4242331 | c.-902A>G | upstream_gene_variant | 1.0 |
| embA | 4242334 | c.-899G>C | upstream_gene_variant | 1.0 |
| embA | 4242343 | c.-890G>C | upstream_gene_variant | 1.0 |
| embA | 4242367 | c.-866C>G | upstream_gene_variant | 0.88 |
| embA | 4242391 | c.-842G>C | upstream_gene_variant | 1.0 |
| embA | 4242394 | c.-839C>T | upstream_gene_variant | 1.0 |
| embA | 4242397 | c.-836G>C | upstream_gene_variant | 1.0 |
| embA | 4242400 | c.-833C>T | upstream_gene_variant | 0.67 |
| embA | 4242403 | c.-830T>G | upstream_gene_variant | 1.0 |
| embA | 4242406 | c.-827A>G | upstream_gene_variant | 1.0 |
| embA | 4242412 | c.-821G>C | upstream_gene_variant | 1.0 |
| embA | 4242421 | c.-812C>T | upstream_gene_variant | 1.0 |
| embA | 4244330 | c.1098G>T | synonymous_variant | 1.0 |
| embA | 4244339 | c.1107G>T | synonymous_variant | 1.0 |
| embA | 4244340 | p.Ser370Ala | missense_variant | 1.0 |
| embA | 4244363 | c.1131C>T | synonymous_variant | 1.0 |
| embA | 4244366 | c.1134C>T | synonymous_variant | 1.0 |
| embA | 4244372 | c.1140T>G | synonymous_variant | 0.8 |
| embA | 4244378 | c.1146G>A | synonymous_variant | 0.8 |
| embA | 4244390 | c.1158G>C | synonymous_variant | 0.8 |
| embA | 4244400 | p.Leu390Val | missense_variant | 0.67 |
| embA | 4244814 | p.Leu528Met | missense_variant | 1.0 |
| embA | 4244838 | c.1606C>T | synonymous_variant | 1.0 |
| embA | 4244843 | c.1611G>A | synonymous_variant | 1.0 |
| embA | 4244849 | c.1617C>T | synonymous_variant | 1.0 |
| embA | 4244855 | c.1623G>A | synonymous_variant | 1.0 |
| embA | 4244861 | c.1629G>T | synonymous_variant | 1.0 |
| embA | 4244862 | c.1630C>T | synonymous_variant | 1.0 |
| embA | 4244865 | p.Ala545Ser | missense_variant | 1.0 |
| embA | 4244873 | c.1641C>G | synonymous_variant | 1.0 |
| embA | 4244885 | c.1653A>G | synonymous_variant | 1.0 |
| embA | 4244897 | c.1665T>C | synonymous_variant | 1.0 |
| embA | 4244900 | c.1668G>C | synonymous_variant | 1.0 |
| embA | 4244903 | c.1671G>A | synonymous_variant | 1.0 |
| embA | 4244904 | p.Val558Ile | missense_variant | 1.0 |
| embA | 4244951 | c.1719G>A | synonymous_variant | 1.0 |
| embA | 4244960 | c.1728A>G | synonymous_variant | 1.0 |
| embA | 4244969 | c.1737G>A | synonymous_variant | 1.0 |
| embA | 4244972 | c.1740G>C | synonymous_variant | 1.0 |
| embA | 4244978 | c.1746G>T | synonymous_variant | 1.0 |
| embA | 4244980 | p.Val583Ala | missense_variant | 0.91 |
| embA | 4244987 | c.1755T>C | synonymous_variant | 1.0 |
| embA | 4244996 | c.1764C>G | synonymous_variant | 1.0 |
| embA | 4245004 | p.Thr591Ser | missense_variant | 1.0 |
| embA | 4245006 | p.Phe592Val | missense_variant | 1.0 |
| embA | 4245014 | c.1782C>G | synonymous_variant | 1.0 |
| embA | 4245020 | c.1788T>C | synonymous_variant | 1.0 |
| embA | 4245023 | c.1791A>G | synonymous_variant | 0.97 |
| embA | 4245047 | c.1815G>C | synonymous_variant | 1.0 |
| embA | 4245051 | p.Val607Ile | missense_variant | 1.0 |
| embA | 4245056 | c.1824C>G | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245089 | c.1857G>C | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245125 | c.1893G>A | synonymous_variant | 1.0 |
| embA | 4245146 | c.1914G>A | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>T | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Phe | missense_variant | 1.0 |
| embA | 4245206 | c.1974A>C | synonymous_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245224 | c.1992T>C | synonymous_variant | 1.0 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 1.0 |
| embA | 4245282 | p.Ile684Val | missense_variant | 1.0 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>C | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 1.0 |
| embA | 4245311 | c.2079C>G | synonymous_variant | 0.97 |
| embA | 4245314 | c.2082G>C | synonymous_variant | 1.0 |
| embA | 4245317 | c.2085G>C | synonymous_variant | 1.0 |
| embA | 4245327 | p.Ala699Leu | missense_variant | 1.0 |
| embA | 4245340 | p.Gly703Ala | missense_variant | 1.0 |
| embA | 4245355 | p.Ala708Gly | missense_variant | 1.0 |
| embA | 4245359 | c.2127G>A | synonymous_variant | 1.0 |
| embA | 4245368 | c.2136T>C | synonymous_variant | 1.0 |
| embA | 4245377 | c.2145T>C | synonymous_variant | 1.0 |
| embA | 4245386 | c.2154C>T | synonymous_variant | 1.0 |
| embA | 4245476 | c.2244C>T | synonymous_variant | 1.0 |
| embA | 4245501 | p.Ala757Lys | missense_variant | 1.0 |
| embA | 4245511 | p.Pro760Arg | missense_variant | 1.0 |
| embA | 4245514 | p.Asp761Ala | missense_variant | 1.0 |
| embB | 4245518 | c.-996A>C | upstream_gene_variant | 1.0 |
| embA | 4245519 | p.Pro763Ala | missense_variant | 1.0 |
| embB | 4245524 | c.-990G>C | upstream_gene_variant | 1.0 |
| embB | 4245530 | c.-984T>C | upstream_gene_variant | 1.0 |
| embA | 4245535 | p.Ser768Asn | missense_variant | 1.0 |
| embB | 4245539 | c.-975C>G | upstream_gene_variant | 1.0 |
| embB | 4245545 | c.-969C>G | upstream_gene_variant | 1.0 |
| embB | 4245560 | c.-954C>T | upstream_gene_variant | 1.0 |
| embB | 4245626 | c.-888G>A | upstream_gene_variant | 1.0 |
| embB | 4245641 | c.-873C>T | upstream_gene_variant | 1.0 |
| embB | 4245644 | c.-870C>G | upstream_gene_variant | 1.0 |
| embA | 4245650 | p.Ile806Met | missense_variant | 1.0 |
| embA | 4245652 | p.Thr807Ser | missense_variant | 1.0 |
| embB | 4245665 | c.-849C>G | upstream_gene_variant | 0.95 |
| embB | 4245668 | c.-846C>G | upstream_gene_variant | 1.0 |
| embB | 4245674 | c.-840A>C | upstream_gene_variant | 1.0 |
| embB | 4245677 | c.-837G>C | upstream_gene_variant | 1.0 |
| embB | 4245683 | c.-831C>G | upstream_gene_variant | 0.96 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245725 | c.-789A>G | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788T>C | upstream_gene_variant | 1.0 |
| embB | 4245731 | c.-783C>T | upstream_gene_variant | 1.0 |
| embB | 4245734 | c.-780G>C | upstream_gene_variant | 1.0 |
| embB | 4245737 | c.-777A>G | upstream_gene_variant | 1.0 |
| embB | 4245755 | c.-759C>G | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.94 |
| embB | 4245782 | c.-732C>G | upstream_gene_variant | 0.93 |
| embB | 4245791 | c.-723C>G | upstream_gene_variant | 0.89 |
| embB | 4246157 | c.-357A>G | upstream_gene_variant | 1.0 |
| embB | 4246164 | c.-350T>C | upstream_gene_variant | 1.0 |
| embB | 4246184 | c.-330A>C | upstream_gene_variant | 1.0 |
| embB | 4246187 | c.-327C>G | upstream_gene_variant | 1.0 |
| embB | 4246190 | c.-324C>T | 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 | 4246208 | c.-306G>A | 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 |
| embB | 4246223 | c.-291C>T | upstream_gene_variant | 1.0 |
| embB | 4246226 | c.-288C>T | upstream_gene_variant | 1.0 |
| embA | 4246227 | p.Ile999Val | missense_variant | 1.0 |
| embB | 4246235 | c.-279G>A | upstream_gene_variant | 1.0 |
| embB | 4246247 | c.-267C>T | upstream_gene_variant | 1.0 |
| embB | 4246259 | c.-255G>C | upstream_gene_variant | 1.0 |
| embB | 4247042 | p.Pro177Asp | missense_variant | 1.0 |
| embB | 4247068 | c.555T>C | synonymous_variant | 1.0 |
| embB | 4247074 | c.561G>C | synonymous_variant | 1.0 |
| embB | 4247086 | c.573C>T | synonymous_variant | 1.0 |
| embB | 4247087 | c.574C>T | synonymous_variant | 1.0 |
| embB | 4247107 | c.594C>G | synonymous_variant | 1.0 |
| embB | 4247114 | p.Ala201Gln | missense_variant | 1.0 |
| embB | 4247117 | p.Val202Leu | missense_variant | 1.0 |
| embB | 4247125 | c.612G>C | synonymous_variant | 1.0 |
| embB | 4247140 | c.627G>A | synonymous_variant | 1.0 |
| embB | 4247150 | c.637C>A | synonymous_variant | 1.0 |
| embB | 4247155 | c.642G>A | synonymous_variant | 1.0 |
| embB | 4247380 | c.867C>G | synonymous_variant | 1.0 |
| embB | 4247395 | c.882C>T | synonymous_variant | 1.0 |
| embB | 4247398 | c.885G>C | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247404 | c.891G>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>C | synonymous_variant | 1.0 |
| embB | 4247446 | c.933C>T | synonymous_variant | 1.0 |
| embB | 4247449 | c.936C>T | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247476 | c.963C>A | synonymous_variant | 0.97 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247527 | c.1014G>A | synonymous_variant | 1.0 |
| embB | 4247541 | p.Val343Gly | missense_variant | 1.0 |
| embB | 4247683 | c.1170C>G | synonymous_variant | 1.0 |
| embB | 4247690 | p.Thr393Ala | missense_variant | 1.0 |
| embB | 4247716 | c.1203C>T | synonymous_variant | 1.0 |
| embB | 4247722 | c.1209G>A | synonymous_variant | 1.0 |
| embB | 4247725 | c.1212G>C | synonymous_variant | 0.96 |
| embB | 4247729 | p.Gly406Pro | missense_variant | 1.0 |
| embB | 4247741 | p.Leu410Val | missense_variant | 1.0 |
| embB | 4247753 | p.Val414Ile | missense_variant | 1.0 |
| embB | 4247773 | c.1260G>A | synonymous_variant | 0.98 |
| embB | 4247785 | c.1272G>A | synonymous_variant | 1.0 |
| embB | 4247795 | c.1282_1284delCTCinsTTG | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>G | synonymous_variant | 1.0 |
| embB | 4247809 | c.1296G>T | synonymous_variant | 1.0 |
| embB | 4247821 | c.1308T>C | synonymous_variant | 1.0 |
| embB | 4247827 | c.1314C>G | synonymous_variant | 1.0 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 1.0 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 1.0 |
| embB | 4247842 | c.1329T>C | synonymous_variant | 1.0 |
| embB | 4247857 | c.1344C>G | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>A | synonymous_variant | 1.0 |
| embB | 4248011 | p.Ser500Arg | missense_variant | 1.0 |
| embB | 4248014 | p.Thr501Ala | missense_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248042 | p.Ala510Gly | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Asp | missense_variant | 1.0 |
| embB | 4248055 | c.1542G>C | synonymous_variant | 1.0 |
| embB | 4248061 | c.1548G>A | synonymous_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248088 | c.1575C>T | synonymous_variant | 1.0 |
| embB | 4248094 | c.1581C>T | synonymous_variant | 1.0 |
| embB | 4248095 | c.1582_1584delCTCinsTTG | synonymous_variant | 1.0 |
| embB | 4248109 | c.1596C>G | synonymous_variant | 1.0 |
| embB | 4248112 | c.1599C>G | synonymous_variant | 1.0 |
| embB | 4248118 | c.1605T>C | synonymous_variant | 1.0 |
| embB | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>G | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248161 | c.1648C>T | synonymous_variant | 1.0 |
| embB | 4248178 | c.1665C>T | synonymous_variant | 1.0 |
| embB | 4248190 | c.1677G>A | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248200 | p.Ile563Val | missense_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248214 | c.1701C>T | synonymous_variant | 1.0 |
| embB | 4248220 | c.1707A>G | synonymous_variant | 1.0 |
| embB | 4248232 | c.1719G>T | synonymous_variant | 0.96 |
| embB | 4248268 | c.1755G>C | synonymous_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248286 | c.1773G>A | synonymous_variant | 1.0 |
| embB | 4248305 | c.1792C>T | synonymous_variant | 1.0 |
| embB | 4248313 | c.1800C>T | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248323 | p.Ala604Ser | missense_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 | 4248361 | c.1848A>G | synonymous_variant | 1.0 |
| embB | 4248362 | p.Ser617Ala | missense_variant | 1.0 |
| embB | 4248389 | p.Met626Val | missense_variant | 1.0 |
| embB | 4248400 | c.1887G>T | synonymous_variant | 1.0 |
| embB | 4248403 | c.1890G>C | synonymous_variant | 1.0 |
| embB | 4248437 | p.Thr642Ser | missense_variant | 1.0 |
| embB | 4248442 | c.1929C>G | synonymous_variant | 1.0 |
| embB | 4248460 | c.1947C>G | synonymous_variant | 1.0 |
| embB | 4248497 | p.Lys662Arg | missense_variant | 1.0 |
| embB | 4248505 | c.1992C>T | synonymous_variant | 1.0 |
| embB | 4248508 | c.1995G>A | synonymous_variant | 1.0 |
| embB | 4248514 | c.2001A>G | synonymous_variant | 1.0 |
| embB | 4248515 | p.Val668Ile | missense_variant | 1.0 |
| embB | 4249369 | c.2856T>C | synonymous_variant | 1.0 |
| embB | 4249381 | c.2868A>G | synonymous_variant | 1.0 |
| embB | 4249387 | c.2874G>A | synonymous_variant | 1.0 |
| embB | 4249394 | p.Ile961Val | missense_variant | 1.0 |
| embB | 4249405 | c.2892C>T | synonymous_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249420 | c.2907G>T | synonymous_variant | 1.0 |
| embB | 4249423 | p.Asp970Glu | missense_variant | 1.0 |
| embB | 4249424 | c.2911C>T | synonymous_variant | 1.0 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 1.0 |
| embB | 4249441 | c.2928A>G | synonymous_variant | 1.0 |
| embB | 4249447 | c.2934G>C | synonymous_variant | 1.0 |
| embB | 4249454 | p.Thr981Ser | missense_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 | 4249487 | c.2974T>C | synonymous_variant | 1.0 |
| embB | 4249525 | c.3012T>C | synonymous_variant | 0.97 |
| embB | 4249529 | p.Ile1006Val | missense_variant | 0.97 |
| embB | 4249532 | p.Ala1007Thr | missense_variant | 0.97 |
| embB | 4249537 | c.3024A>G | synonymous_variant | 0.97 |
| embB | 4249540 | c.3027C>T | synonymous_variant | 0.97 |
| embB | 4249558 | c.3045A>G | synonymous_variant | 0.97 |
| embB | 4249568 | p.Ser1019Thr | missense_variant | 0.92 |
| embB | 4249573 | c.3060T>C | synonymous_variant | 0.96 |
| embB | 4249581 | p.Leu1023Gln | missense_variant | 0.96 |
| embB | 4249594 | c.3081G>C | synonymous_variant | 1.0 |
| embB | 4249600 | c.3087A>G | synonymous_variant | 1.0 |
| embB | 4249607 | p.Thr1032Val | missense_variant | 1.0 |
| embB | 4249618 | c.3105C>T | synonymous_variant | 1.0 |
| embB | 4249627 | c.3114G>C | synonymous_variant | 0.94 |
| embB | 4249637 | p.Leu1042Val | missense_variant | 0.94 |
| embB | 4249640 | c.3127T>C | synonymous_variant | 0.94 |
| embB | 4249648 | c.3135G>C | synonymous_variant | 0.94 |
| embB | 4249651 | c.3138C>G | synonymous_variant | 0.94 |
| embB | 4249657 | c.3144C>G | synonymous_variant | 0.94 |
| embB | 4249663 | c.3150C>G | synonymous_variant | 0.94 |
| embB | 4249686 | p.Ala1058Gly | missense_variant | 0.92 |
| embB | 4249690 | c.3177C>T | synonymous_variant | 0.9 |
| embB | 4249693 | c.3180T>C | synonymous_variant | 0.89 |
| embB | 4249699 | c.3186T>G | synonymous_variant | 0.89 |
| embB | 4249702 | c.3189C>G | synonymous_variant | 0.89 |
| aftB | 4267148 | c.1689A>G | synonymous_variant | 1.0 |
| aftB | 4267154 | c.1683A>G | synonymous_variant | 1.0 |
| aftB | 4267159 | p.Thr560Ala | missense_variant | 1.0 |
| aftB | 4267169 | p.Gln556Ala | missense_variant | 1.0 |
| aftB | 4267177 | p.Ile554Leu | missense_variant | 1.0 |
| aftB | 4267181 | c.1656C>A | synonymous_variant | 1.0 |
| aftB | 4267189 | p.Ile550Val | missense_variant | 1.0 |
| aftB | 4267190 | c.1647T>C | synonymous_variant | 1.0 |
| aftB | 4267196 | c.1641C>T | synonymous_variant | 1.0 |
| aftB | 4267205 | c.1632G>C | synonymous_variant | 1.0 |
| aftB | 4267211 | c.1626C>A | synonymous_variant | 1.0 |
| aftB | 4267214 | c.1623A>C | synonymous_variant | 1.0 |
| aftB | 4267241 | c.1596G>C | synonymous_variant | 1.0 |
| aftB | 4267541 | c.1296C>T | synonymous_variant | 1.0 |
| aftB | 4267544 | c.1293T>C | synonymous_variant | 1.0 |
| aftB | 4267556 | c.1281G>C | synonymous_variant | 1.0 |
| aftB | 4267586 | c.1251C>G | synonymous_variant | 1.0 |
| aftB | 4267607 | c.1230G>A | synonymous_variant | 1.0 |
| aftB | 4267625 | c.1212T>C | synonymous_variant | 0.97 |
| aftB | 4267628 | c.1209C>G | synonymous_variant | 1.0 |
| aftB | 4267655 | c.1182C>A | synonymous_variant | 1.0 |
| aftB | 4267667 | c.1170A>G | synonymous_variant | 1.0 |
| aftB | 4267793 | c.1044C>A | synonymous_variant | 1.0 |
| aftB | 4267796 | c.1041G>C | synonymous_variant | 1.0 |
| aftB | 4267801 | c.1036T>C | synonymous_variant | 1.0 |
| aftB | 4267816 | p.Ala341Thr | missense_variant | 1.0 |
| aftB | 4267822 | c.1015T>C | synonymous_variant | 1.0 |
| aftB | 4267823 | c.1014G>T | synonymous_variant | 1.0 |
| aftB | 4267838 | c.999T>C | synonymous_variant | 1.0 |
| aftB | 4267841 | c.996C>T | synonymous_variant | 1.0 |
| aftB | 4267844 | c.993C>A | synonymous_variant | 1.0 |
| aftB | 4267850 | c.987A>G | synonymous_variant | 1.0 |
| aftB | 4268063 | c.774G>C | synonymous_variant | 1.0 |
| aftB | 4268068 | p.Val257Leu | missense_variant | 1.0 |
| aftB | 4268069 | c.768C>T | synonymous_variant | 1.0 |
| aftB | 4268077 | p.Met254Val | missense_variant | 1.0 |
| aftB | 4268081 | c.756A>G | synonymous_variant | 1.0 |
| aftB | 4268099 | c.738G>C | synonymous_variant | 1.0 |
| aftB | 4268102 | c.735C>G | 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>C | synonymous_variant | 1.0 |
| aftB | 4268138 | c.699A>G | synonymous_variant | 1.0 |
| aftB | 4268144 | c.693T>C | synonymous_variant | 1.0 |
| aftB | 4268164 | p.Gln225Glu | missense_variant | 1.0 |
| aftB | 4268165 | c.672C>T | synonymous_variant | 1.0 |
| aftB | 4268169 | p.Ala223Gly | missense_variant | 1.0 |
| aftB | 4268177 | p.Leu220Phe | missense_variant | 1.0 |
| aftB | 4268180 | p.Phe219Leu | missense_variant | 1.0 |
| aftB | 4268183 | c.654A>G | synonymous_variant | 1.0 |
| aftB | 4268194 | p.Leu215Val | missense_variant | 1.0 |
| aftB | 4268207 | c.630C>G | synonymous_variant | 1.0 |
| aftB | 4268386 | c.451T>C | synonymous_variant | 1.0 |
| aftB | 4268393 | c.444G>C | synonymous_variant | 1.0 |
| aftB | 4268404 | p.Leu145Met | missense_variant | 1.0 |
| aftB | 4268414 | c.423C>T | synonymous_variant | 1.0 |
| aftB | 4268417 | c.420G>A | synonymous_variant | 1.0 |
| aftB | 4268420 | c.417G>C | synonymous_variant | 1.0 |
| aftB | 4268423 | c.414C>G | synonymous_variant | 1.0 |
| aftB | 4268429 | c.408C>G | synonymous_variant | 1.0 |
| aftB | 4268438 | c.399C>T | synonymous_variant | 1.0 |
| aftB | 4268441 | c.396C>T | synonymous_variant | 1.0 |
| aftB | 4268444 | c.393C>G | synonymous_variant | 1.0 |
| aftB | 4268450 | c.387A>G | synonymous_variant | 1.0 |
| aftB | 4268462 | c.375T>C | synonymous_variant | 1.0 |
| aftB | 4268985 | c.-149A>G | upstream_gene_variant | 1.0 |
| aftB | 4268999 | c.-163C>T | upstream_gene_variant | 1.0 |
| aftB | 4269006 | c.-170T>C | 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 | 4269021 | c.-185C>G | upstream_gene_variant | 1.0 |
| aftB | 4269027 | c.-191C>A | upstream_gene_variant | 1.0 |
| aftB | 4269033 | c.-197T>C | upstream_gene_variant | 1.0 |
| aftB | 4269042 | c.-206G>C | upstream_gene_variant | 1.0 |
| aftB | 4269057 | c.-221C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |
| aftB | 4269096 | c.-260C>G | upstream_gene_variant | 1.0 |
| aftB | 4269099 | c.-263G>C | upstream_gene_variant | 1.0 |
| aftB | 4269102 | c.-268_-266delAGCinsTCG | upstream_gene_variant | 1.0 |
| ubiA | 4269110 | p.Gly242Arg | missense_variant | 1.0 |
| aftB | 4269114 | c.-278C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269143 | p.Leu231Val | missense_variant | 1.0 |
| aftB | 4269144 | c.-308C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269149 | p.Val229Leu | missense_variant | 1.0 |
| aftB | 4269153 | c.-317C>G | upstream_gene_variant | 1.0 |
| aftB | 4269156 | c.-320C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269164 | p.Leu224Met | missense_variant | 1.0 |
| aftB | 4269165 | c.-329G>C | upstream_gene_variant | 1.0 |
| aftB | 4269171 | c.-335C>T | upstream_gene_variant | 1.0 |
| aftB | 4269186 | c.-350C>G | upstream_gene_variant | 1.0 |
| aftB | 4269192 | c.-356C>G | upstream_gene_variant | 1.0 |
| aftB | 4269201 | c.-365A>G | upstream_gene_variant | 1.0 |
| aftB | 4269206 | c.-370C>T | upstream_gene_variant | 1.0 |
| aftB | 4269210 | c.-374G>A | upstream_gene_variant | 1.0 |
| ubiA | 4269220 | p.Ala205Lys | missense_variant | 1.0 |
| aftB | 4269222 | c.-386T>C | upstream_gene_variant | 1.0 |
| aftB | 4269242 | c.-406C>T | upstream_gene_variant | 1.0 |
| aftB | 4269249 | c.-413G>A | upstream_gene_variant | 1.0 |
| aftB | 4269258 | c.-422C>T | upstream_gene_variant | 1.0 |
| aftB | 4269264 | c.-428C>G | upstream_gene_variant | 1.0 |
| aftB | 4269282 | c.-446G>A | upstream_gene_variant | 1.0 |
| ubiA | 4269357 | p.Ile159Leu | missense_variant | 1.0 |
| aftB | 4269375 | c.-539G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269380 | p.Val152Ile | missense_variant | 1.0 |
| aftB | 4269384 | c.-548C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| ubiA | 4269390 | p.Val148Ile | 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 | 4269408 | c.-572C>G | upstream_gene_variant | 1.0 |
| aftB | 4269411 | c.-575T>G | upstream_gene_variant | 0.75 |
| aftB | 4269414 | c.-578T>C | upstream_gene_variant | 1.0 |
| aftB | 4269428 | c.-592T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269448 | p.Val129Ala | missense_variant | 1.0 |
| aftB | 4269453 | c.-617A>G | upstream_gene_variant | 1.0 |
| ubiA | 4269478 | p.Met119Trp | missense_variant | 1.0 |
| ubiA | 4269485 | p.Ala117Ser | missense_variant | 1.0 |
| ubiA | 4269486 | p.Gly116Val | missense_variant | 1.0 |
| ubiA | 4269490 | p.Ala115Val | missense_variant | 1.0 |
| ubiA | 4269498 | p.Thr112Ala | missense_variant | 1.0 |
| aftB | 4269507 | c.-671G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269513 | p.Val107Ala | missense_variant | 1.0 |
| ubiA | 4269521 | p.Val105Leu | missense_variant | 1.0 |
| aftB | 4269528 | c.-692G>C | upstream_gene_variant | 1.0 |
| aftB | 4269537 | c.-701G>A | upstream_gene_variant | 1.0 |
| aftB | 4269572 | c.-736A>C | upstream_gene_variant | 1.0 |
| aftB | 4269582 | c.-746C>T | upstream_gene_variant | 1.0 |
| aftB | 4269588 | c.-752G>C | upstream_gene_variant | 1.0 |
| aftB | 4269594 | c.-758A>C | upstream_gene_variant | 1.0 |
| aftB | 4269597 | c.-761G>A | upstream_gene_variant | 1.0 |
| aftB | 4269600 | c.-764C>G | upstream_gene_variant | 1.0 |
| aftB | 4269603 | c.-767C>T | upstream_gene_variant | 1.0 |
| aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
| aftB | 4269609 | c.-773G>T | upstream_gene_variant | 1.0 |
| ubiA | 4269620 | p.Val72Ile | missense_variant | 1.0 |
| aftB | 4269621 | c.-785C>G | upstream_gene_variant | 1.0 |
| aftB | 4269624 | c.-788C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269632 | p.Ala68Ser | missense_variant | 1.0 |
| ubiA | 4269647 | p.Ser63Cys | missense_variant | 1.0 |
| ubiA | 4269684 | p.Glu50Asp | missense_variant | 1.0 |
| ubiA | 4269689 | p.Val49Leu | missense_variant | 1.0 |
| ubiA | 4269705 | p.Gly43Asp | missense_variant | 1.0 |
| ubiA | 4269709 | p.Gly42Thr | missense_variant | 1.0 |
| aftB | 4269716 | c.-880T>C | upstream_gene_variant | 1.0 |
| aftB | 4269720 | c.-884C>T | upstream_gene_variant | 1.0 |
| aftB | 4269726 | c.-890G>A | upstream_gene_variant | 1.0 |
| ubiA | 4269733 | p.Ala34Gly | missense_variant | 1.0 |
| ubiA | 4269746 | p.Val30Leu | missense_variant | 1.0 |
| aftB | 4269750 | c.-914A>G | upstream_gene_variant | 1.0 |
| aftB | 4269759 | c.-923G>A | upstream_gene_variant | 1.0 |
| aftB | 4269762 | c.-926C>G | upstream_gene_variant | 1.0 |
| aftB | 4269786 | c.-950G>C | upstream_gene_variant | 0.83 |
| ethA | 4326280 | c.1194G>A | synonymous_variant | 1.0 |
| ethA | 4326295 | c.1179G>C | synonymous_variant | 1.0 |
| ethA | 4326298 | c.1176G>A | synonymous_variant | 1.0 |
| ethA | 4326307 | c.1167C>G | synonymous_variant | 1.0 |
| ethA | 4326310 | c.1164T>C | synonymous_variant | 1.0 |
| ethA | 4326319 | c.1155C>T | synonymous_variant | 1.0 |
| ethA | 4326322 | p.Val384Ile | missense_variant | 1.0 |
| ethA | 4326325 | c.1149G>C | synonymous_variant | 1.0 |
| ethA | 4326329 | p.Tyr382Phe | missense_variant | 1.0 |
| ethA | 4326331 | c.1143C>G | synonymous_variant | 1.0 |
| ethA | 4326340 | c.1134C>G | synonymous_variant | 1.0 |
| ethA | 4326343 | p.Ile377Met | missense_variant | 1.0 |
| ethA | 4326351 | p.Ser375Thr | missense_variant | 1.0 |
| ethA | 4326352 | c.1122T>G | synonymous_variant | 1.0 |
| ethR | 4327375 | c.-174G>C | upstream_gene_variant | 1.0 |
| ethA | 4327387 | p.Thr29Ser | missense_variant | 1.0 |
| ethR | 4327396 | c.-153A>G | upstream_gene_variant | 1.0 |
| ethA | 4327425 | p.Val17Ile | missense_variant | 1.0 |
| ethR | 4327435 | c.-114T>G | upstream_gene_variant | 1.0 |
| ethR | 4327438 | c.-111A>G | upstream_gene_variant | 1.0 |
| ethR | 4327459 | c.-90G>A | upstream_gene_variant | 1.0 |
| ethR | 4327665 | p.Asp39Glu | missense_variant | 1.0 |
| ethA | 4327674 | c.-201C>G | upstream_gene_variant | 1.0 |
| ethA | 4327680 | c.-207A>G | upstream_gene_variant | 1.0 |
| ethA | 4327695 | c.-222A>G | upstream_gene_variant | 1.0 |
| ethA | 4327707 | c.-234G>C | upstream_gene_variant | 1.0 |
| ethA | 4327710 | c.-237G>C | upstream_gene_variant | 1.0 |
| ethA | 4327713 | c.-240A>G | upstream_gene_variant | 1.0 |
| ethR | 4327714 | p.Ile56Leu | missense_variant | 1.0 |
| ethA | 4327719 | c.-246C>G | upstream_gene_variant | 1.0 |
| ethA | 4327720 | c.-249_-247delCCTinsGCG | upstream_gene_variant | 1.0 |
| ethA | 4327746 | c.-273T>G | upstream_gene_variant | 1.0 |
| ethR | 4327755 | p.Glu69Asp | missense_variant | 1.0 |
| ethA | 4327761 | c.-288C>T | upstream_gene_variant | 1.0 |
| ethA | 4327764 | c.-291C>G | upstream_gene_variant | 1.0 |
| ethA | 4328419 | c.-946G>C | upstream_gene_variant | 1.0 |
| ethA | 4328425 | c.-952C>G | upstream_gene_variant | 1.0 |
| ethA | 4328429 | c.-956C>A | upstream_gene_variant | 1.0 |
| ethA | 4328435 | c.-962C>T | upstream_gene_variant | 1.0 |
| ethA | 4328455 | c.-982G>C | upstream_gene_variant | 1.0 |
| ethA | 4328471 | c.-998A>G | upstream_gene_variant | 1.0 |
| ethA | 4328473 | c.-1000G>C | upstream_gene_variant | 1.0 |
