Run ID: ERR6359082
Sample name:
Date: 21-01-2022 08:20:24
Number of reads: 905982
Percentage reads mapped: 21.21
Strain: lineage4.9
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.05 |
| lineage5.1.2 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.98 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| gyrB | 6738 | p.Thr500Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6170 | p.His311Ala | missense_variant | 1.0 |
| gyrB | 6178 | c.939C>T | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>G | synonymous_variant | 1.0 |
| gyrB | 6203 | c.964_966delAGCinsTCG | synonymous_variant | 1.0 |
| gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
| gyrB | 6215 | c.976_978delTCGinsAGC | synonymous_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6238 | c.999G>A | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>G | synonymous_variant | 1.0 |
| gyrB | 6283 | p.Asp348Glu | missense_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 6304 | c.-998C>G | upstream_gene_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6310 | c.-992G>C | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrB | 6324 | c.1085_1086insGTCC | frameshift_variant | 1.0 |
| gyrB | 6327 | c.1090_1093delGAAC | frameshift_variant | 1.0 |
| gyrA | 6358 | c.-944C>G | upstream_gene_variant | 1.0 |
| gyrA | 6361 | c.-941G>A | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6619 | c.-683T>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6628 | c.-674C>G | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>C | upstream_gene_variant | 1.0 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>T | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6680 | c.-622C>T | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6706 | c.-596G>A | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6715 | c.-587C>G | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>C | 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 | 6764 | c.-538C>T | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6802 | c.-500G>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 | 6853 | c.-449A>G | 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 | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421T>C | upstream_gene_variant | 1.0 |
| gyrA | 6889 | c.-413G>T | upstream_gene_variant | 1.0 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6922 | c.-380G>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 | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7114 | c.-188C>G | upstream_gene_variant | 1.0 |
| gyrA | 7120 | c.-182T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>G | upstream_gene_variant | 1.0 |
| gyrB | 7124 | p.Ser629Thr | missense_variant | 1.0 |
| gyrA | 7129 | c.-173T>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7147 | c.-155G>C | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>C | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7159 | c.-143C>T | upstream_gene_variant | 1.0 |
| gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
| gyrA | 7171 | c.-131C>T | upstream_gene_variant | 1.0 |
| gyrA | 7177 | c.-125G>A | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124_-122delTTGinsCTC | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
| gyrA | 7213 | c.-89G>T | upstream_gene_variant | 1.0 |
| gyrA | 7352 | c.51G>A | synonymous_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7412 | c.111C>G | synonymous_variant | 1.0 |
| gyrA | 7418 | c.117C>T | synonymous_variant | 1.0 |
| gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
| gyrA | 7433 | c.132G>C | 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 | 7472 | c.171T>C | 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 | 7496 | c.195C>G | synonymous_variant | 1.0 |
| gyrA | 7502 | c.201C>T | synonymous_variant | 1.0 |
| gyrA | 7517 | c.216G>A | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>C | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7569 | p.Ala90Ser | missense_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 | 7614 | c.313C>T | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>T | synonymous_variant | 1.0 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7706 | c.405C>T | synonymous_variant | 1.0 |
| gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 1.0 |
| gyrA | 7758 | p.Ile153Val | missense_variant | 1.0 |
| gyrA | 7763 | c.462T>G | synonymous_variant | 1.0 |
| gyrA | 7769 | c.468C>T | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>C | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7841 | c.540C>T | synonymous_variant | 1.0 |
| gyrA | 7853 | c.552C>T | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>G | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7880 | c.579C>T | synonymous_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8253 | p.Ile318Val | missense_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8318 | c.1017C>G | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8327 | c.1026C>T | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>C | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8366 | c.1065G>C | synonymous_variant | 1.0 |
| gyrA | 8378 | c.1077C>T | synonymous_variant | 1.0 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8401 | p.Asp367Ala | missense_variant | 1.0 |
| gyrA | 8417 | c.1116C>G | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8426 | c.1125G>A | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>C | synonymous_variant | 1.0 |
| gyrA | 8465 | c.1164C>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8600 | c.1299G>A | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8627 | c.1326C>G | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>G | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8649 | p.Arg450Lys | missense_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8708 | c.1407G>C | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8717 | c.1416C>G | synonymous_variant | 1.0 |
| gyrA | 8720 | c.1419G>A | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8740 | p.Arg480Gln | missense_variant | 1.0 |
| gyrA | 8742 | p.Asp481Gln | missense_variant | 1.0 |
| gyrA | 8756 | c.1455A>G | synonymous_variant | 1.0 |
| gyrA | 8762 | c.1461G>C | synonymous_variant | 1.0 |
| gyrA | 8765 | p.Asp488Glu | missense_variant | 0.97 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 0.97 |
| gyrA | 8769 | p.His490Tyr | missense_variant | 1.0 |
| gyrA | 8783 | c.1482G>T | synonymous_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8817 | p.Ser506Ala | missense_variant | 1.0 |
| gyrA | 8822 | c.1521C>T | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>G | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>T | synonymous_variant | 1.0 |
| gyrA | 8882 | c.1581G>A | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8966 | c.1665C>G | synonymous_variant | 1.0 |
| gyrA | 8981 | c.1680G>C | synonymous_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9020 | c.1719G>A | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>G | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9063 | p.Ser588Leu | missense_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9074 | c.1773G>T | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>T | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9101 | c.1800A>G | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9144 | p.Arg615Lys | missense_variant | 1.0 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 1.0 |
| gyrA | 9161 | c.1860C>G | synonymous_variant | 1.0 |
| gyrA | 9167 | c.1866C>T | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9191 | c.1890G>C | synonymous_variant | 1.0 |
| gyrA | 9197 | c.1896G>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9227 | c.1926C>G | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9236 | c.1935G>C | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
| gyrA | 9248 | c.1947G>C | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9266 | p.Asp655Glu | missense_variant | 1.0 |
| gyrA | 9267 | p.Asn656Gly | missense_variant | 1.0 |
| gyrA | 9275 | c.1974G>A | synonymous_variant | 1.0 |
| gyrA | 9278 | c.1977G>C | synonymous_variant | 1.0 |
| gyrA | 9288 | p.Val663Met | missense_variant | 1.0 |
| gyrA | 9291 | c.1990C>T | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9299 | c.1998G>C | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
| gyrA | 9308 | c.2007C>T | synonymous_variant | 1.0 |
| gyrA | 9311 | c.2010C>T | synonymous_variant | 1.0 |
| gyrA | 9318 | c.2017C>T | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9345 | c.2044A>C | synonymous_variant | 1.0 |
| fgd1 | 491176 | c.394C>T | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491184 | c.402A>G | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491194 | c.412_414delCTAinsTTG | 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 | 491223 | c.441C>G | synonymous_variant | 1.0 |
| fgd1 | 491229 | c.447C>T | synonymous_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 1.0 |
| fgd1 | 491248 | p.Arg156Thr | missense_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491262 | c.480C>G | synonymous_variant | 1.0 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
| fgd1 | 491289 | c.507C>G | synonymous_variant | 1.0 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 1.0 |
| fgd1 | 491307 | c.525C>G | synonymous_variant | 1.0 |
| fgd1 | 491310 | c.528C>G | synonymous_variant | 1.0 |
| fgd1 | 491316 | c.534C>G | synonymous_variant | 1.0 |
| fgd1 | 491320 | p.Ala180Thr | missense_variant | 1.0 |
| fgd1 | 491331 | c.549G>A | synonymous_variant | 1.0 |
| fgd1 | 491340 | c.558C>G | synonymous_variant | 1.0 |
| fgd1 | 491343 | c.561C>G | synonymous_variant | 1.0 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
| fgd1 | 491382 | c.600G>A | synonymous_variant | 1.0 |
| fgd1 | 491415 | c.633A>G | synonymous_variant | 1.0 |
| fgd1 | 491418 | c.636A>C | synonymous_variant | 1.0 |
| fgd1 | 491424 | c.642C>T | synonymous_variant | 1.0 |
| fgd1 | 491427 | c.645C>G | synonymous_variant | 1.0 |
| fgd1 | 491430 | c.648T>G | synonymous_variant | 1.0 |
| fgd1 | 491436 | c.654T>C | synonymous_variant | 1.0 |
| fgd1 | 491439 | p.Asp219Glu | missense_variant | 1.0 |
| fgd1 | 491443 | p.Ser221Asp | missense_variant | 1.0 |
| fgd1 | 491454 | c.672C>G | synonymous_variant | 1.0 |
| fgd1 | 491472 | c.690A>G | synonymous_variant | 1.0 |
| fgd1 | 491493 | c.711C>G | synonymous_variant | 1.0 |
| fgd1 | 491499 | c.717G>A | synonymous_variant | 1.0 |
| fgd1 | 491503 | c.721C>T | synonymous_variant | 1.0 |
| fgd1 | 491508 | c.726A>G | synonymous_variant | 1.0 |
| fgd1 | 491509 | c.727T>C | synonymous_variant | 1.0 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491535 | c.753G>A | synonymous_variant | 1.0 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 1.0 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
| fgd1 | 491548 | p.Ala256Pro | missense_variant | 1.0 |
| fgd1 | 491553 | c.771G>A | synonymous_variant | 1.0 |
| fgd1 | 491563 | c.781_783delAGCinsTCG | synonymous_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| mshA | 575714 | p.Tyr123Asn | missense_variant | 1.0 |
| mshA | 575732 | c.385_387delCTTinsTTG | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575749 | c.402C>G | synonymous_variant | 1.0 |
| mshA | 575770 | c.423G>C | synonymous_variant | 1.0 |
| mshA | 575772 | p.Val142Ala | missense_variant | 1.0 |
| mshA | 575779 | c.432A>G | synonymous_variant | 1.0 |
| mshA | 575782 | c.435G>C | synonymous_variant | 1.0 |
| mshA | 575785 | c.438T>C | synonymous_variant | 0.97 |
| mshA | 575795 | p.Ile150Val | missense_variant | 1.0 |
| mshA | 575803 | c.456C>T | synonymous_variant | 1.0 |
| mshA | 575812 | c.465C>T | synonymous_variant | 1.0 |
| mshA | 575818 | c.471G>C | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
| mshA | 575824 | c.477T>C | synonymous_variant | 1.0 |
| mshA | 575842 | c.495G>C | synonymous_variant | 0.97 |
| mshA | 575843 | p.Arg166Ala | missense_variant | 1.0 |
| mshA | 575864 | c.517T>C | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>G | synonymous_variant | 1.0 |
| mshA | 575884 | c.537G>C | synonymous_variant | 1.0 |
| mshA | 575892 | p.Ala182Gly | missense_variant | 1.0 |
| mshA | 575908 | c.561A>C | synonymous_variant | 1.0 |
| mshA | 575916 | p.Asp190Val | missense_variant | 1.0 |
| mshA | 575920 | c.573C>G | synonymous_variant | 1.0 |
| mshA | 575924 | p.Gly193Ser | missense_variant | 1.0 |
| mshA | 575929 | c.582C>G | synonymous_variant | 1.0 |
| mshA | 575932 | c.585G>A | synonymous_variant | 1.0 |
| mshA | 575939 | p.Leu198Met | missense_variant | 1.0 |
| mshA | 575944 | c.597T>C | synonymous_variant | 1.0 |
| mshA | 575945 | p.Thr200Ser | missense_variant | 1.0 |
| mshA | 575953 | c.606G>C | synonymous_variant | 1.0 |
| mshA | 575959 | c.612G>A | synonymous_variant | 1.0 |
| mshA | 575980 | c.633T>C | synonymous_variant | 1.0 |
| rpoB | 760088 | c.282C>G | synonymous_variant | 0.95 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>G | synonymous_variant | 1.0 |
| rpoB | 760130 | c.324T>C | synonymous_variant | 1.0 |
| rpoB | 760139 | c.333A>T | synonymous_variant | 1.0 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 1.0 |
| rpoB | 760148 | p.Asp114Glu | missense_variant | 1.0 |
| rpoB | 760155 | p.Lys117Arg | missense_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760199 | c.393C>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_512delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760334 | c.528G>C | synonymous_variant | 1.0 |
| rpoB | 760337 | c.531C>G | synonymous_variant | 0.94 |
| rpoB | 760340 | c.534G>C | synonymous_variant | 0.94 |
| rpoB | 760354 | p.Glu183Ala | missense_variant | 1.0 |
| rpoB | 760357 | p.Thr184Asn | missense_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760389 | c.583_585delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 760407 | p.Ser201Gly | missense_variant | 1.0 |
| rpoB | 760418 | c.612G>C | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760449 | p.Thr215Leu | missense_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760463 | c.657C>G | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760527 | p.Gln241Ala | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Arg | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760587 | p.Thr261Ala | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760593 | p.Gly263Asn | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760643 | c.837G>A | synonymous_variant | 1.0 |
| rpoB | 760649 | c.843G>C | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | 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 | 760718 | c.912C>G | synonymous_variant | 1.0 |
| rpoB | 760721 | c.915C>G | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760734 | p.Val310Ile | missense_variant | 1.0 |
| rpoB | 760916 | c.1110C>G | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760964 | c.1158C>G | synonymous_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>T | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761021 | c.1215G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | 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 | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>G | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>G | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>G | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761201 | c.1395G>A | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>T | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761222 | c.1416G>C | 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>T | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761339 | c.1533C>G | synonymous_variant | 1.0 |
| rpoB | 761342 | p.Lys512Asn | missense_variant | 1.0 |
| rpoB | 761345 | c.1539G>T | synonymous_variant | 1.0 |
| rpoB | 761348 | c.1542C>G | synonymous_variant | 1.0 |
| rpoB | 761357 | c.1551G>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761369 | p.Glu521Asp | missense_variant | 1.0 |
| rpoB | 761374 | p.Val523Glu | missense_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761414 | c.1608A>G | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761430 | p.Ile542Leu | missense_variant | 1.0 |
| rpoB | 761435 | p.Asp543Glu | missense_variant | 1.0 |
| rpoB | 761437 | p.Ala544Asp | missense_variant | 1.0 |
| rpoB | 761444 | c.1638T>C | synonymous_variant | 1.0 |
| rpoB | 761451 | p.Val549Thr | missense_variant | 1.0 |
| rpoB | 761457 | p.Pro551Glu | missense_variant | 1.0 |
| rpoB | 761477 | c.1671C>T | synonymous_variant | 1.0 |
| rpoB | 761482 | p.Ala559Gly | missense_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761502 | p.Pro566Ser | missense_variant | 1.0 |
| rpoB | 761508 | p.Ser568Ala | missense_variant | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | 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 | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761640 | c.1834C>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761660 | c.1854G>A | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761682 | c.1876C>T | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>G | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761705 | c.1899C>T | synonymous_variant | 1.0 |
| rpoB | 761711 | c.1905C>G | synonymous_variant | 1.0 |
| rpoB | 761712 | p.Val636Ile | missense_variant | 1.0 |
| rpoB | 761732 | c.1926C>T | synonymous_variant | 1.0 |
| rpoB | 761747 | c.1941G>C | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>G | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761790 | p.Arg662Thr | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761814 | p.Ala670Asn | missense_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 | 761868 | p.Asp688Gln | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>T | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761892 | p.Ile696Val | missense_variant | 1.0 |
| rpoB | 761897 | c.2091C>G | synonymous_variant | 1.0 |
| rpoB | 761903 | c.2097T>C | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761930 | c.2124G>C | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761987 | c.2181C>T | synonymous_variant | 1.0 |
| rpoB | 762006 | c.2200_2202delCGCinsAGG | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762024 | p.Val740Thr | missense_variant | 1.0 |
| rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
| rpoB | 762129 | c.2323_2325delCTCinsTTG | synonymous_variant | 1.0 |
| rpoB | 762134 | c.2328C>A | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762209 | c.2403C>T | synonymous_variant | 1.0 |
| rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762281 | c.2475G>A | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>C | upstream_gene_variant | 1.0 |
| rpoC | 762380 | c.-990T>G | upstream_gene_variant | 1.0 |
| rpoC | 762392 | c.-978G>A | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762407 | c.-963G>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762490 | p.Val895Ala | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.96 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 0.96 |
| rpoC | 762521 | c.-849C>G | upstream_gene_variant | 1.0 |
| rpoC | 762527 | c.-843G>C | 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 | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762557 | c.-813G>C | upstream_gene_variant | 1.0 |
| rpoC | 762560 | c.-810A>T | upstream_gene_variant | 1.0 |
| rpoC | 762563 | c.-807G>T | upstream_gene_variant | 1.0 |
| rpoB | 762735 | p.Ala977Asn | missense_variant | 1.0 |
| rpoC | 762753 | c.-617_-615delTTGinsCTC | upstream_gene_variant | 1.0 |
| rpoC | 762758 | c.-612G>C | upstream_gene_variant | 1.0 |
| rpoB | 762760 | p.Cys985Ser | missense_variant | 1.0 |
| rpoB | 762768 | p.Pro988Ala | missense_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762785 | p.Asp993Glu | missense_variant | 1.0 |
| rpoB | 762786 | p.Val994Ile | missense_variant | 1.0 |
| rpoB | 762789 | p.Leu995Met | missense_variant | 1.0 |
| rpoB | 762795 | p.Asp997Asn | missense_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762814 | p.Met1003Lys | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 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 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoC | 762902 | c.-468C>T | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.99 |
| 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 | 763049 | c.-321G>A | upstream_gene_variant | 1.0 |
| rpoC | 763058 | c.-312C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763130 | c.-240G>A | upstream_gene_variant | 1.0 |
| rpoC | 763133 | c.-237G>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763178 | c.-192G>A | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>T | upstream_gene_variant | 1.0 |
| rpoB | 763203 | p.Ser1133Ala | missense_variant | 1.0 |
| rpoB | 763207 | p.Ser1134Lys | missense_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763262 | c.-108C>A | upstream_gene_variant | 1.0 |
| rpoC | 763265 | c.-105G>C | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
| rpoC | 763351 | c.-19T>C | upstream_gene_variant | 1.0 |
| rpoC | 763352 | c.-18T>A | upstream_gene_variant | 1.0 |
| rpoC | 763396 | c.27A>G | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>G | synonymous_variant | 1.0 |
| rpoC | 763430 | c.61A>C | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 0.99 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763561 | c.192G>A | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763621 | c.252C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>A | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>C | synonymous_variant | 1.0 |
| rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>T | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763933 | c.564C>T | synonymous_variant | 1.0 |
| rpoC | 763936 | c.567C>G | synonymous_variant | 1.0 |
| rpoC | 763939 | c.570G>A | synonymous_variant | 1.0 |
| rpoC | 763947 | p.Ala193Val | missense_variant | 1.0 |
| rpoC | 763972 | c.603C>T | synonymous_variant | 1.0 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764029 | p.Glu220Asp | missense_variant | 1.0 |
| rpoC | 764030 | p.Asp221Asn | missense_variant | 1.0 |
| rpoC | 764039 | p.Ser224Asp | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764048 | p.Thr227Val | missense_variant | 1.0 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 1.0 |
| rpoC | 764080 | c.711C>T | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764085 | p.Asn239Thr | missense_variant | 1.0 |
| rpoC | 764087 | p.Leu240Val | missense_variant | 1.0 |
| rpoC | 764095 | c.726C>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764104 | c.735C>G | synonymous_variant | 1.0 |
| rpoC | 764110 | c.741C>T | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 1.0 |
| rpoC | 764143 | c.774G>C | synonymous_variant | 1.0 |
| rpoC | 764169 | p.Asn267Thr | missense_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764207 | p.Val280Thr | missense_variant | 1.0 |
| rpoC | 764213 | p.Arg282Lys | missense_variant | 1.0 |
| rpoC | 764242 | c.873C>T | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764269 | c.900G>C | synonymous_variant | 1.0 |
| rpoC | 764272 | c.903G>C | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764293 | c.924G>C | synonymous_variant | 1.0 |
| rpoC | 764317 | c.948C>G | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>G | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764429 | c.1060C>T | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066A>C | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764455 | c.1086G>T | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764515 | c.1146C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764551 | c.1182G>C | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764578 | c.1209C>G | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>A | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764705 | c.1336C>T | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>A | 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>G | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764863 | c.1494G>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>T | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764896 | c.1527C>T | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 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 | 765052 | c.1683C>G | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>C | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>T | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>A | synonymous_variant | 1.0 |
| rpoC | 765121 | c.1752G>A | synonymous_variant | 1.0 |
| rpoC | 765359 | p.Ala664Thr | missense_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765445 | c.2076G>T | synonymous_variant | 1.0 |
| rpoC | 765453 | p.Ala695Val | missense_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765508 | c.2139C>G | synonymous_variant | 1.0 |
| rpoC | 765547 | c.2178C>T | 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 | 765562 | c.2193G>C | synonymous_variant | 1.0 |
| rpoC | 765565 | c.2196G>C | synonymous_variant | 0.98 |
| rpoC | 765607 | c.2238C>G | synonymous_variant | 1.0 |
| rpoC | 765611 | p.His748Ser | missense_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765640 | c.2271A>G | synonymous_variant | 1.0 |
| rpoC | 765662 | c.2293_2295delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765718 | p.Asp783Glu | missense_variant | 1.0 |
| rpoC | 765724 | c.2355C>G | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>T | synonymous_variant | 1.0 |
| rpoC | 765742 | p.Glu791Asp | missense_variant | 1.0 |
| rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
| rpoC | 765753 | p.Asp795Ala | missense_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 | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765850 | c.2481G>C | synonymous_variant | 1.0 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765884 | c.2515_2516delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Gly | missense_variant | 1.0 |
| rpoC | 766061 | p.Val898Leu | missense_variant | 1.0 |
| rpoC | 766066 | c.2697C>G | synonymous_variant | 1.0 |
| rpoC | 766069 | c.2700G>A | synonymous_variant | 1.0 |
| rpoC | 766079 | p.Arg904Val | missense_variant | 1.0 |
| rpoC | 766084 | c.2715A>T | synonymous_variant | 1.0 |
| rpoC | 766085 | p.Pro906Ala | missense_variant | 1.0 |
| rpoC | 766093 | c.2724C>T | synonymous_variant | 1.0 |
| rpoC | 766094 | p.Thr909Ser | missense_variant | 1.0 |
| rpoC | 766113 | p.Tyr915Phe | missense_variant | 1.0 |
| rpoC | 766270 | c.2901G>C | synonymous_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766291 | c.2922G>C | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>G | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpoC | 766480 | c.3111C>G | synonymous_variant | 1.0 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766517 | p.Thr1050Ala | missense_variant | 1.0 |
| rpoC | 766522 | c.3153C>A | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766530 | p.Arg1054Gln | missense_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766546 | p.Glu1059Asp | missense_variant | 1.0 |
| rpoC | 766547 | p.Arg1060Lys | missense_variant | 1.0 |
| rpoC | 766564 | c.3195C>G | synonymous_variant | 1.0 |
| rpoC | 766570 | c.3201T>G | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>G | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>T | synonymous_variant | 1.0 |
| rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766610 | p.Ser1081Pro | missense_variant | 1.0 |
| rpoC | 766618 | c.3249G>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
| rpoC | 766664 | c.3295_3297delCTCinsTTG | synonymous_variant | 1.0 |
| rpoC | 766667 | p.Ser1100Ala | missense_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766675 | c.3306C>T | synonymous_variant | 1.0 |
| rpoC | 766690 | c.3321G>C | synonymous_variant | 1.0 |
| rpoC | 766693 | c.3324C>A | synonymous_variant | 1.0 |
| rpoC | 766702 | c.3333G>C | synonymous_variant | 1.0 |
| rpoC | 766708 | c.3339A>G | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766750 | c.3381C>G | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766771 | c.3402G>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766775 | p.Arg1136Lys | missense_variant | 1.0 |
| rpoC | 766787 | p.Glu1140Gln | missense_variant | 1.0 |
| rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766846 | c.3477C>G | synonymous_variant | 1.0 |
| rpoC | 766883 | p.Ser1172Ala | missense_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766911 | p.Ile1181Thr | missense_variant | 1.0 |
| rpoC | 766915 | p.Asp1182Glu | missense_variant | 1.0 |
| rpoC | 766921 | c.3552G>C | synonymous_variant | 1.0 |
| rpoC | 766931 | p.Ala1188Thr | missense_variant | 1.0 |
| rpoC | 766942 | c.3573C>T | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766978 | c.3609C>G | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>G | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767023 | c.3654C>T | synonymous_variant | 1.0 |
| rpoC | 767032 | c.3663G>C | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767105 | p.Asn1246Gln | missense_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767152 | c.3783T>C | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>G | synonymous_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 | 767212 | c.3843G>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767230 | c.3861G>C | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767266 | c.3897G>C | synonymous_variant | 1.0 |
| rpoC | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>T | synonymous_variant | 0.93 |
| rpoC | 767302 | c.3933C>G | synonymous_variant | 1.0 |
| rpsL | 781589 | c.30G>A | synonymous_variant | 1.0 |
| rpsL | 781592 | c.33T>C | 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>G | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781664 | c.105C>T | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>G | synonymous_variant | 1.0 |
| rpsL | 781724 | c.165G>C | synonymous_variant | 1.0 |
| rpsL | 781726 | p.Lys56Arg | missense_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 | 781748 | c.189C>G | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 0.98 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>T | synonymous_variant | 1.0 |
| rpsL | 781784 | c.225G>A | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781863 | c.304C>T | 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>G | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>G | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>C | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | 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 | 800744 | c.-65G>C | 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 | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800873 | p.Arg22Lys | missense_variant | 1.0 |
| rplC | 800877 | c.69A>C | synonymous_variant | 1.0 |
| rplC | 800880 | c.72A>G | synonymous_variant | 1.0 |
| rplC | 800886 | c.78G>C | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800892 | c.84G>C | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| rplC | 800931 | c.123G>C | synonymous_variant | 1.0 |
| rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
| rplC | 800946 | c.138T>C | synonymous_variant | 1.0 |
| rplC | 800950 | c.142_144delAGCinsTCG | synonymous_variant | 1.0 |
| rplC | 800964 | c.156G>C | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800985 | c.177A>T | synonymous_variant | 1.0 |
| rplC | 801009 | c.201A>C | synonymous_variant | 1.0 |
| rplC | 801019 | p.Thr71Ala | missense_variant | 1.0 |
| rplC | 801030 | c.222C>G | synonymous_variant | 1.0 |
| rplC | 801039 | c.231A>G | synonymous_variant | 1.0 |
| rplC | 801045 | c.237A>G | synonymous_variant | 1.0 |
| rplC | 801046 | p.Tyr80His | missense_variant | 1.0 |
| rplC | 801054 | c.246G>C | synonymous_variant | 1.0 |
| rplC | 801058 | c.250C>T | synonymous_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801176 | p.Phe123Tyr | missense_variant | 1.0 |
| rplC | 801205 | p.Arg133Ala | missense_variant | 1.0 |
| rplC | 801220 | p.Ser138Gly | missense_variant | 1.0 |
| rplC | 801228 | c.420T>C | synonymous_variant | 1.0 |
| rplC | 801231 | c.423C>T | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>G | synonymous_variant | 1.0 |
| rplC | 801255 | c.447C>T | synonymous_variant | 1.0 |
| rplC | 801258 | c.450C>G | synonymous_variant | 1.0 |
| rplC | 801267 | c.459A>T | synonymous_variant | 1.0 |
| rplC | 801270 | c.462T>C | synonymous_variant | 1.0 |
| rplC | 801271 | p.Ala155Ser | missense_variant | 1.0 |
| rplC | 801276 | c.468G>C | synonymous_variant | 1.0 |
| rplC | 801281 | p.Ala158Gly | missense_variant | 1.0 |
| rplC | 801307 | p.Ala167Ser | missense_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| fbiC | 1303435 | c.505_506delTCinsAG | synonymous_variant | 1.0 |
| fbiC | 1303441 | c.511T>C | synonymous_variant | 1.0 |
| fbiC | 1303444 | p.Ser172Ala | missense_variant | 1.0 |
| fbiC | 1303455 | c.525C>A | synonymous_variant | 1.0 |
| fbiC | 1303458 | c.528G>C | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>C | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303488 | c.558G>C | synonymous_variant | 1.0 |
| fbiC | 1303492 | c.562T>C | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 0.98 |
| fbiC | 1303512 | c.582T>G | synonymous_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303554 | c.624G>A | synonymous_variant | 1.0 |
| fbiC | 1303560 | c.630G>C | synonymous_variant | 1.0 |
| fbiC | 1303581 | c.651G>C | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303602 | c.672A>G | synonymous_variant | 1.0 |
| fbiC | 1303613 | p.Leu228Gln | missense_variant | 1.0 |
| fbiC | 1303617 | c.687C>A | 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 | 1303650 | c.720G>A | synonymous_variant | 1.0 |
| fbiC | 1303659 | c.729T>C | synonymous_variant | 1.0 |
| fbiC | 1303660 | p.Val244Thr | missense_variant | 1.0 |
| fbiC | 1303666 | p.Thr246Ala | missense_variant | 1.0 |
| fbiC | 1303671 | c.741C>T | synonymous_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303680 | c.750G>C | synonymous_variant | 1.0 |
| fbiC | 1303681 | c.751_753delTTGinsCTC | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303689 | c.759T>C | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303704 | c.774T>C | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303731 | c.801A>G | synonymous_variant | 1.0 |
| fbiC | 1303732 | p.Ser268Ala | missense_variant | 1.0 |
| fbiC | 1303746 | c.816T>C | synonymous_variant | 1.0 |
| fbiC | 1303749 | c.819G>C | synonymous_variant | 1.0 |
| fbiC | 1303750 | p.Leu274Val | missense_variant | 1.0 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303768 | p.Ser280Val | missense_variant | 1.0 |
| fbiC | 1303788 | c.858T>C | synonymous_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 1.0 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303824 | c.894G>A | synonymous_variant | 1.0 |
| fbiC | 1303827 | c.897A>G | synonymous_variant | 1.0 |
| fbiC | 1304517 | c.1587C>T | synonymous_variant | 1.0 |
| fbiC | 1304520 | c.1590A>C | synonymous_variant | 1.0 |
| fbiC | 1304526 | c.1596T>G | synonymous_variant | 1.0 |
| fbiC | 1304532 | c.1602G>A | synonymous_variant | 1.0 |
| fbiC | 1304538 | c.1608C>T | synonymous_variant | 1.0 |
| fbiC | 1304544 | p.Asp538Glu | missense_variant | 1.0 |
| fbiC | 1304546 | p.Val539Ala | missense_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
| fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
| fbiC | 1304583 | c.1653C>T | synonymous_variant | 1.0 |
| fbiC | 1304604 | c.1674C>T | synonymous_variant | 1.0 |
| fbiC | 1304607 | c.1677C>T | synonymous_variant | 1.0 |
| fbiC | 1304608 | p.Thr560Val | missense_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304845 | p.Ala639Thr | missense_variant | 1.0 |
| fbiC | 1304853 | c.1923C>G | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304857 | p.Thr643Ser | missense_variant | 1.0 |
| fbiC | 1304868 | c.1938G>C | synonymous_variant | 1.0 |
| fbiC | 1304869 | c.1939C>T | synonymous_variant | 1.0 |
| fbiC | 1304874 | c.1944C>T | synonymous_variant | 1.0 |
| fbiC | 1304880 | c.1950C>G | synonymous_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304910 | c.1980G>C | synonymous_variant | 1.0 |
| fbiC | 1304915 | p.Asp662Gly | missense_variant | 1.0 |
| fbiC | 1304918 | p.Thr663Ser | missense_variant | 1.0 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 1.0 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 1.0 |
| fbiC | 1304943 | c.2013C>T | synonymous_variant | 1.0 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 1.0 |
| fbiC | 1304949 | c.2019C>T | synonymous_variant | 1.0 |
| fbiC | 1304956 | p.Val676Ile | missense_variant | 1.0 |
| fbiC | 1305249 | c.2319G>C | synonymous_variant | 1.0 |
| fbiC | 1305259 | c.2329T>C | synonymous_variant | 1.0 |
| fbiC | 1305267 | c.2337C>G | synonymous_variant | 1.0 |
| fbiC | 1305274 | p.Ser782Pro | missense_variant | 1.0 |
| fbiC | 1305277 | p.His783Asn | missense_variant | 1.0 |
| fbiC | 1305282 | c.2352T>C | synonymous_variant | 1.0 |
| fbiC | 1305297 | c.2367G>C | synonymous_variant | 1.0 |
| fbiC | 1305300 | c.2370A>G | synonymous_variant | 1.0 |
| fbiC | 1305303 | c.2373T>G | synonymous_variant | 1.0 |
| fbiC | 1305306 | c.2376A>G | synonymous_variant | 1.0 |
| fbiC | 1305310 | p.Arg794Glu | missense_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305348 | c.2418C>T | synonymous_variant | 1.0 |
| fbiC | 1305360 | c.2430G>C | synonymous_variant | 1.0 |
| fbiC | 1305381 | c.2451G>C | synonymous_variant | 1.0 |
| fbiC | 1305390 | c.2460C>G | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>C | synonymous_variant | 1.0 |
| fbiC | 1305399 | c.2469A>G | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>C | synonymous_variant | 1.0 |
| fbiC | 1305418 | p.Val830Ile | missense_variant | 1.0 |
| fbiC | 1305426 | c.2496G>A | synonymous_variant | 1.0 |
| fbiC | 1305432 | c.2502C>G | synonymous_variant | 1.0 |
| fbiC | 1305434 | p.Ala835Gly | missense_variant | 1.0 |
| fbiC | 1305444 | c.2514A>G | synonymous_variant | 1.0 |
| fbiC | 1305462 | c.2532G>T | synonymous_variant | 1.0 |
| atpE | 1460850 | c.-195_-193delCTCinsATG | upstream_gene_variant | 1.0 |
| atpE | 1460855 | c.-190T>C | upstream_gene_variant | 1.0 |
| atpE | 1460858 | c.-187C>G | upstream_gene_variant | 1.0 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1460888 | c.-157C>A | upstream_gene_variant | 1.0 |
| atpE | 1460897 | c.-148A>G | upstream_gene_variant | 1.0 |
| atpE | 1460900 | c.-145T>C | upstream_gene_variant | 1.0 |
| atpE | 1461056 | c.12T>A | synonymous_variant | 1.0 |
| atpE | 1461062 | c.18T>G | synonymous_variant | 1.0 |
| atpE | 1461086 | c.42A>C | synonymous_variant | 1.0 |
| atpE | 1461089 | c.45G>C | synonymous_variant | 1.0 |
| atpE | 1461107 | c.63C>G | synonymous_variant | 1.0 |
| atpE | 1461113 | c.69C>T | synonymous_variant | 1.0 |
| atpE | 1461131 | c.87T>C | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461137 | c.93C>G | synonymous_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461158 | c.114T>A | synonymous_variant | 1.0 |
| atpE | 1461159 | p.Val39Ile | missense_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461182 | c.138A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>C | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471926 | n.81C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472042 | n.197T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472292 | n.447A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472298 | n.453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472302 | n.457_458insT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472310 | n.465_466insG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472683 | n.838_839insTA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>T | 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 | 1473111 | n.1266A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473792 | n.135C>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473812 | n.155G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474026 | n.369C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474094 | n.437C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474108 | n.451C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474110 | n.453A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474287 | n.630_631insTC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_646delCCTCTCCGGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>G | 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 | 1474350 | n.693G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474421 | n.764G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474427 | n.770A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474432 | n.775C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474452 | n.795C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474711 | n.1054G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474713 | n.1056T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474715 | n.1058_1059insC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474952 | n.1296delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474957 | n.1301_1308delACCTTGTG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474990 | n.1333C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474991 | n.1334T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474995 | n.1338T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474997 | n.1340A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474999 | n.1342C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475008 | n.1351C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475010 | n.1353G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475037 | n.1380T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475062 | n.1405A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475375 | n.1718G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475403 | n.1746T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475404 | n.1747A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475407 | n.1750C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475409 | n.1752T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475428 | n.1771G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475433 | n.1776A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475458 | n.1801C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | 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 | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475603 | n.1946G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475612 | n.1955G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475614 | n.1957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475619 | n.1962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475621 | n.1964T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475629 | n.1972G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | 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 | 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>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476108 | n.2451T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476246 | n.2589G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476262 | n.2605G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.99 |
| 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>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476679 | n.3022T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476746 | n.3089T>A | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1674443 | p.Ala81Val | missense_variant | 1.0 |
| inhA | 1674452 | p.Ala84Glu | missense_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674507 | c.306G>C | synonymous_variant | 1.0 |
| inhA | 1674514 | p.Ile105Val | missense_variant | 1.0 |
| inhA | 1674534 | c.333G>C | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674550 | p.Ser117Ala | missense_variant | 1.0 |
| inhA | 1674579 | c.378G>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
| inhA | 1674588 | c.387G>A | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674601 | p.Leu134Thr | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>G | synonymous_variant | 1.0 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674690 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1833547 | c.6G>A | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833658 | c.117C>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833730 | c.189C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833770 | p.Asn77His | missense_variant | 1.0 |
| rpsA | 1833778 | c.237C>G | synonymous_variant | 0.99 |
| rpsA | 1833781 | c.240T>G | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833814 | c.273C>G | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>C | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833892 | c.351G>A | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834018 | c.477C>T | synonymous_variant | 1.0 |
| rpsA | 1834039 | c.498C>T | synonymous_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Arg | missense_variant | 1.0 |
| rpsA | 1834051 | c.510G>A | synonymous_variant | 1.0 |
| rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 0.98 |
| 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 | 1834172 | p.Ile211Val | 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 | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>G | 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 | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>T | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>C | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | 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 | 1834522 | c.981C>T | synonymous_variant | 1.0 |
| rpsA | 1834525 | c.984G>A | synonymous_variant | 1.0 |
| rpsA | 1834527 | p.Arg329Gln | missense_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834558 | c.1017C>G | synonymous_variant | 1.0 |
| rpsA | 1834573 | c.1032G>C | synonymous_variant | 1.0 |
| rpsA | 1834603 | p.Glu354Asp | missense_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834666 | c.1125G>C | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834751 | p.Leu404Ile | missense_variant | 1.0 |
| rpsA | 1834759 | c.1218A>T | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | 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 | 1834837 | p.Met432Ile | missense_variant | 1.0 |
| kasA | 2517917 | c.-198G>C | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517956 | c.-159G>A | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2518216 | c.102G>A | synonymous_variant | 1.0 |
| kasA | 2518219 | c.105T>C | synonymous_variant | 1.0 |
| kasA | 2518231 | c.117C>T | synonymous_variant | 1.0 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 1.0 |
| kasA | 2518240 | c.126C>A | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_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 | 2518290 | p.Lys59Arg | missense_variant | 1.0 |
| kasA | 2518300 | c.186T>G | synonymous_variant | 1.0 |
| kasA | 2518303 | c.189C>T | synonymous_variant | 1.0 |
| kasA | 2518309 | c.195G>A | synonymous_variant | 1.0 |
| kasA | 2518312 | c.198T>C | synonymous_variant | 1.0 |
| kasA | 2518322 | p.Ser70Asp | missense_variant | 1.0 |
| kasA | 2518336 | c.222A>G | synonymous_variant | 1.0 |
| kasA | 2518337 | c.223_225delCTCinsTTG | synonymous_variant | 1.0 |
| kasA | 2518343 | p.Met77Leu | missense_variant | 1.0 |
| kasA | 2518348 | c.234A>G | synonymous_variant | 1.0 |
| kasA | 2518488 | p.Ser125Thr | missense_variant | 1.0 |
| kasA | 2518492 | c.378C>T | 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 | 2518561 | c.447T>C | synonymous_variant | 1.0 |
| kasA | 2518567 | c.453G>C | synonymous_variant | 1.0 |
| kasA | 2518570 | c.456G>A | synonymous_variant | 1.0 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
| kasA | 2518579 | c.465T>G | synonymous_variant | 1.0 |
| kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518606 | c.492G>C | synonymous_variant | 1.0 |
| kasA | 2518609 | p.Met165Ile | missense_variant | 1.0 |
| kasA | 2518642 | c.528A>G | 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>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
| kasA | 2518688 | p.Val192Phe | missense_variant | 1.0 |
| kasA | 2518705 | c.591T>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518715 | p.Pro201Gly | missense_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518739 | p.Ala209Thr | missense_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518756 | c.642G>C | synonymous_variant | 1.0 |
| kasA | 2518759 | c.645C>G | synonymous_variant | 1.0 |
| kasA | 2518780 | p.Glu222Asp | missense_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518787 | p.Arg225Gly | missense_variant | 1.0 |
| kasA | 2518816 | c.702C>G | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518843 | c.729T>C | synonymous_variant | 1.0 |
| kasA | 2518847 | p.Leu245Met | missense_variant | 1.0 |
| kasA | 2518853 | p.Leu247Ile | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| ahpC | 2726558 | c.366A>C | synonymous_variant | 1.0 |
| ahpC | 2726564 | c.372C>G | synonymous_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
| ahpC | 2726591 | c.399C>G | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726648 | c.456T>C | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | c.477T>C | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 1.0 |
| folC | 2747023 | c.576C>G | synonymous_variant | 1.0 |
| folC | 2747029 | c.570G>C | synonymous_variant | 1.0 |
| folC | 2747035 | p.Asn188Glu | missense_variant | 1.0 |
| folC | 2747040 | p.Ile187Val | missense_variant | 1.0 |
| folC | 2747041 | c.558G>C | synonymous_variant | 1.0 |
| folC | 2747059 | c.540T>C | synonymous_variant | 1.0 |
| folC | 2747062 | c.537A>C | synonymous_variant | 1.0 |
| folC | 2747071 | c.528C>G | synonymous_variant | 1.0 |
| folC | 2747074 | c.525G>C | synonymous_variant | 1.0 |
| folC | 2747080 | c.519C>G | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>C | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
| folC | 2747098 | c.501C>T | synonymous_variant | 1.0 |
| folC | 2747101 | c.498G>C | synonymous_variant | 1.0 |
| folC | 2747107 | c.492G>C | synonymous_variant | 1.0 |
| folC | 2747110 | c.489T>C | synonymous_variant | 1.0 |
| folC | 2747113 | c.486C>G | synonymous_variant | 1.0 |
| folC | 2747122 | c.477G>C | synonymous_variant | 1.0 |
| folC | 2747129 | p.Ala157Gly | missense_variant | 1.0 |
| folC | 2747155 | c.444G>C | synonymous_variant | 1.0 |
| thyX | 3067706 | c.240C>T | synonymous_variant | 1.0 |
| thyX | 3067709 | c.235_237delTCGinsAGC | synonymous_variant | 1.0 |
| thyX | 3067717 | p.Ser77Gly | missense_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyX | 3067730 | c.216G>C | synonymous_variant | 1.0 |
| thyX | 3067739 | c.207T>C | synonymous_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 1.0 |
| thyX | 3067763 | c.183C>G | synonymous_variant | 1.0 |
| thyX | 3067769 | p.Gly59Ala | missense_variant | 1.0 |
| thyX | 3067787 | p.Lys53Arg | missense_variant | 1.0 |
| thyX | 3067790 | c.156C>G | synonymous_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067823 | c.123G>A | synonymous_variant | 1.0 |
| thyX | 3067847 | p.Pro33Gln | missense_variant | 1.0 |
| thyX | 3067850 | c.96A>T | synonymous_variant | 1.0 |
| thyX | 3067856 | p.Asp30Glu | missense_variant | 1.0 |
| thyX | 3067869 | p.Thr26Ser | missense_variant | 1.0 |
| thyX | 3067874 | p.Pro24Ala | missense_variant | 1.0 |
| thyX | 3067877 | c.69G>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 | p.Ala19Pro | missense_variant | 1.0 |
| thyX | 3067892 | c.54G>A | synonymous_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyX | 3067910 | c.36C>T | synonymous_variant | 1.0 |
| thyX | 3067924 | p.Arg8Gly | missense_variant | 1.0 |
| thyX | 3067927 | c.19C>T | synonymous_variant | 1.0 |
| thyX | 3067934 | c.12C>G | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>G | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073874 | p.Ile200Val | missense_variant | 1.0 |
| thyA | 3073881 | c.591C>A | synonymous_variant | 1.0 |
| thyA | 3073887 | p.Ser195Asp | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073893 | c.579C>G | synonymous_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073993 | c.478_479delAGinsTC | synonymous_variant | 1.0 |
| thyA | 3074001 | c.471C>G | synonymous_variant | 1.0 |
| thyA | 3074004 | p.Asp156Gly | missense_variant | 1.0 |
| thyA | 3074027 | p.Phe149Leu | missense_variant | 1.0 |
| thyA | 3074028 | c.444G>A | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074042 | p.Pro144Ala | missense_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074055 | p.Glu139Asp | missense_variant | 1.0 |
| thyA | 3074058 | p.Ile138Leu | missense_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| thyA | 3074082 | c.390G>C | synonymous_variant | 1.0 |
| thyA | 3074094 | c.378G>C | synonymous_variant | 1.0 |
| fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640768 | p.Gln76Glu | missense_variant | 1.0 |
| fbiB | 3640782 | c.-753C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640785 | p.Gln81His | missense_variant | 1.0 |
| fbiB | 3640788 | c.-747T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640794 | c.-741A>G | upstream_gene_variant | 1.0 |
| fbiB | 3640797 | c.-738T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640810 | p.Gln90Glu | missense_variant | 1.0 |
| fbiB | 3640815 | c.-720A>G | upstream_gene_variant | 1.0 |
| fbiB | 3640816 | c.-719C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640820 | p.Val93Ala | missense_variant | 1.0 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640830 | c.-705C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640831 | p.Val97Met | missense_variant | 1.0 |
| fbiB | 3640836 | c.-699G>A | upstream_gene_variant | 1.0 |
| fbiB | 3640839 | c.-696C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640850 | p.Glu103Gly | missense_variant | 1.0 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640869 | c.-666G>C | upstream_gene_variant | 1.0 |
| ddn | 3986648 | c.-196C>G | upstream_gene_variant | 1.0 |
| ddn | 3986661 | c.-183C>A | upstream_gene_variant | 1.0 |
| ddn | 3986663 | c.-180_-177delAGCC | upstream_gene_variant | 1.0 |
| ddn | 3986690 | c.-154C>G | upstream_gene_variant | 1.0 |
| ddn | 3986699 | c.-145C>G | upstream_gene_variant | 1.0 |
| panD | 4044126 | c.156T>C | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044147 | c.135C>G | 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 | 4044188 | c.94T>C | synonymous_variant | 1.0 |
| panD | 4044210 | c.72C>A | synonymous_variant | 1.0 |
| panD | 4044232 | p.Cys17His | missense_variant | 1.0 |
| embC | 4240717 | c.855T>C | synonymous_variant | 1.0 |
| embC | 4240736 | c.874_875delTCinsAG | synonymous_variant | 1.0 |
| embC | 4240747 | c.885C>T | synonymous_variant | 1.0 |
| embC | 4240765 | c.903C>G | synonymous_variant | 1.0 |
| embC | 4240768 | c.906G>C | synonymous_variant | 1.0 |
| embC | 4240769 | p.Val303Ile | missense_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240800 | p.Tyr313Phe | missense_variant | 1.0 |
| embC | 4240819 | c.957A>C | synonymous_variant | 1.0 |
| embC | 4240822 | c.960C>G | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4241071 | c.1209C>G | synonymous_variant | 1.0 |
| embC | 4241084 | p.Leu408Ala | missense_variant | 1.0 |
| embC | 4241104 | c.1242G>A | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>A | synonymous_variant | 1.0 |
| embC | 4241134 | c.1272G>A | synonymous_variant | 1.0 |
| embC | 4241135 | p.Val425Leu | missense_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Val | 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 | 4241167 | c.1305C>G | synonymous_variant | 1.0 |
| embC | 4241185 | c.1323G>C | synonymous_variant | 1.0 |
| embC | 4241188 | c.1326C>G | synonymous_variant | 1.0 |
| embC | 4241197 | c.1335G>C | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
| embC | 4241210 | c.1348C>T | synonymous_variant | 1.0 |
| embC | 4241215 | c.1353C>G | synonymous_variant | 1.0 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 1.0 |
| embC | 4241233 | c.1371G>C | synonymous_variant | 1.0 |
| embC | 4241240 | c.1378C>T | synonymous_variant | 0.94 |
| embA | 4242826 | c.-407G>C | upstream_gene_variant | 1.0 |
| embA | 4242832 | c.-401A>G | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242847 | c.-386C>G | upstream_gene_variant | 1.0 |
| embA | 4242862 | c.-371A>G | upstream_gene_variant | 1.0 |
| embC | 4242863 | p.Tyr1001Asn | missense_variant | 1.0 |
| embA | 4242868 | c.-365C>G | upstream_gene_variant | 1.0 |
| embA | 4242871 | c.-362C>G | upstream_gene_variant | 1.0 |
| embC | 4242872 | p.Asp1004Thr | missense_variant | 1.0 |
| embC | 4242878 | p.Thr1006Val | missense_variant | 1.0 |
| embA | 4242907 | c.-326G>C | upstream_gene_variant | 1.0 |
| embA | 4242919 | c.-314A>G | upstream_gene_variant | 1.0 |
| embA | 4242922 | c.-311C>G | upstream_gene_variant | 1.0 |
| embA | 4242928 | c.-305A>G | upstream_gene_variant | 1.0 |
| embA | 4242940 | c.-293T>C | upstream_gene_variant | 1.0 |
| embC | 4242941 | p.His1027Asn | missense_variant | 1.0 |
| embA | 4242946 | c.-287T>C | upstream_gene_variant | 1.0 |
| embA | 4242976 | c.-257G>A | upstream_gene_variant | 1.0 |
| embA | 4242977 | c.-256C>T | upstream_gene_variant | 1.0 |
| embC | 4242980 | p.Met1040Val | missense_variant | 1.0 |
| embA | 4242988 | c.-245A>G | upstream_gene_variant | 1.0 |
| embC | 4242998 | p.Ala1046Pro | missense_variant | 1.0 |
| embA | 4243006 | c.-227C>T | upstream_gene_variant | 1.0 |
| embA | 4243009 | c.-224C>G | upstream_gene_variant | 1.0 |
| embC | 4243012 | p.Lys1050Asn | missense_variant | 1.0 |
| embC | 4243013 | p.Asp1051His | missense_variant | 1.0 |
| embA | 4243024 | c.-209T>C | upstream_gene_variant | 1.0 |
| embA | 4243025 | c.-208A>C | upstream_gene_variant | 1.0 |
| embA | 4243036 | c.-197C>T | upstream_gene_variant | 1.0 |
| embA | 4243040 | c.-193_-191delTTAinsCTG | upstream_gene_variant | 1.0 |
| embC | 4243047 | p.Arg1062Gln | missense_variant | 1.0 |
| embA | 4244858 | c.1626G>C | synonymous_variant | 1.0 |
| embA | 4244862 | p.Leu544Val | missense_variant | 1.0 |
| embA | 4244873 | c.1641C>G | synonymous_variant | 1.0 |
| embA | 4244876 | c.1644G>C | synonymous_variant | 1.0 |
| embA | 4244885 | c.1653A>G | synonymous_variant | 1.0 |
| embA | 4244894 | c.1662C>G | synonymous_variant | 1.0 |
| embA | 4244897 | c.1665T>G | synonymous_variant | 1.0 |
| embA | 4244906 | c.1674C>G | synonymous_variant | 1.0 |
| embA | 4244909 | c.1677C>A | synonymous_variant | 1.0 |
| embA | 4244919 | c.1687_1689delCTCinsTTG | synonymous_variant | 1.0 |
| embA | 4244930 | c.1698G>C | synonymous_variant | 1.0 |
| embA | 4244933 | c.1701A>G | synonymous_variant | 1.0 |
| embA | 4244945 | c.1713C>G | synonymous_variant | 1.0 |
| embA | 4244959 | p.Ala576Gly | missense_variant | 1.0 |
| embA | 4244980 | p.Val583Ala | missense_variant | 1.0 |
| embA | 4244982 | c.1750T>C | synonymous_variant | 1.0 |
| embA | 4244986 | p.Gly585Ala | missense_variant | 1.0 |
| embA | 4244999 | c.1767G>C | synonymous_variant | 1.0 |
| embA | 4245008 | c.1776T>C | synonymous_variant | 1.0 |
| embA | 4245015 | p.Ile595Val | missense_variant | 1.0 |
| embA | 4245020 | c.1788T>G | synonymous_variant | 1.0 |
| embA | 4245023 | c.1791A>G | synonymous_variant | 1.0 |
| embA | 4245026 | c.1794T>C | synonymous_variant | 1.0 |
| embA | 4245029 | c.1797T>C | synonymous_variant | 1.0 |
| embA | 4245039 | p.Leu603Met | missense_variant | 1.0 |
| embA | 4245050 | c.1818C>T | synonymous_variant | 1.0 |
| embB | 4247395 | c.882C>G | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247425 | c.912G>C | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>G | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>G | synonymous_variant | 1.0 |
| embB | 4247446 | c.933C>T | synonymous_variant | 1.0 |
| embB | 4247462 | c.949_950delTCinsAG | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248173 | p.Val554Met | missense_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248202 | c.1689T>C | synonymous_variant | 1.0 |
| embB | 4248203 | p.Pro564Ala | missense_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248215 | p.Arg568Ser | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>G | synonymous_variant | 1.0 |
| embB | 4248225 | p.Ala571Val | missense_variant | 1.0 |
| embB | 4248248 | p.Phe579Leu | missense_variant | 1.0 |
| embB | 4248252 | p.Gly580Ala | missense_variant | 1.0 |
| embB | 4248256 | c.1743C>G | synonymous_variant | 1.0 |
| embB | 4248264 | p.Phe584Ser | missense_variant | 1.0 |
| embB | 4248274 | c.1761C>T | synonymous_variant | 1.0 |
| embB | 4248275 | p.Thr588Ala | missense_variant | 1.0 |
| embB | 4248338 | c.1825C>T | synonymous_variant | 1.0 |
| embB | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4248368 | p.Leu619Val | missense_variant | 1.0 |
| mshA | 554009 | c.-21338_*17562del | transcript_ablation | 1.0 |
| fabG1 | 1672171 | c.-1268_229del | frameshift_variant | 1.0 |
| inhA | 1673799 | c.-402_238del | frameshift_variant&start_lost | 1.0 |
