Run ID: SRR1173484
Sample name:
Date: 03-04-2023 03:25:45
Number of reads: 58565
Percentage reads mapped: 19.61
Strain: lineage4
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5326 | c.87T>C | synonymous_variant | 1.0 |
| gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
| gyrB | 5344 | c.105C>G | synonymous_variant | 1.0 |
| gyrB | 5347 | c.108G>C | synonymous_variant | 1.0 |
| gyrB | 5353 | c.114T>C | synonymous_variant | 1.0 |
| gyrB | 5359 | c.120C>T | synonymous_variant | 1.0 |
| gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
| gyrB | 5371 | c.132T>C | synonymous_variant | 1.0 |
| gyrB | 5377 | c.138T>C | synonymous_variant | 1.0 |
| gyrB | 5396 | p.Ala53Ser | missense_variant | 1.0 |
| gyrB | 5419 | c.180T>C | synonymous_variant | 1.0 |
| gyrB | 6100 | c.861G>C | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6123 | p.Ala295Gly | missense_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6136 | c.897G>A | synonymous_variant | 1.0 |
| gyrB | 6139 | c.900G>C | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>T | synonymous_variant | 1.0 |
| gyrB | 6238 | c.999G>A | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6248 | c.1009_1011delCTAinsTTG | synonymous_variant | 1.0 |
| gyrB | 6256 | c.1017G>A | synonymous_variant | 1.0 |
| gyrB | 6268 | c.1029C>G | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6289 | c.1050C>T | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrA | 6346 | c.-956C>T | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6376 | c.-926G>A | upstream_gene_variant | 1.0 |
| gyrA | 6379 | c.-923C>G | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 1.0 |
| gyrA | 6670 | c.-632G>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6910 | c.-392G>A | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
| gyrA | 6952 | c.-350C>G | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>C | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | upstream_gene_variant | 1.0 |
| gyrA | 7010 | c.-292C>T | upstream_gene_variant | 1.0 |
| gyrA | 7015 | c.-287G>A | upstream_gene_variant | 1.0 |
| gyrA | 7018 | c.-284G>A | upstream_gene_variant | 1.0 |
| gyrB | 7023 | p.Leu595Gln | missense_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7147 | c.-155G>C | upstream_gene_variant | 1.0 |
| gyrA | 7165 | c.-137C>G | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
| gyrA | 7334 | c.33G>C | synonymous_variant | 1.0 |
| gyrA | 7335 | p.Leu12Val | missense_variant | 1.0 |
| gyrA | 7347 | p.Glu16Gln | missense_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7361 | c.60C>T | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 1.0 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>A | synonymous_variant | 1.0 |
| gyrA | 8093 | c.792C>T | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>A | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
| gyrA | 8129 | c.828T>C | synonymous_variant | 1.0 |
| gyrA | 8135 | c.834C>G | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8330 | c.1029C>G | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8372 | c.1071G>C | synonymous_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
| gyrA | 8387 | c.1086C>T | synonymous_variant | 1.0 |
| gyrA | 8391 | p.Tyr364His | missense_variant | 1.0 |
| gyrA | 8399 | c.1098T>G | synonymous_variant | 1.0 |
| gyrA | 8401 | p.Asp367Ala | missense_variant | 1.0 |
| gyrA | 8405 | c.1104C>T | synonymous_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8579 | c.1278C>T | synonymous_variant | 1.0 |
| gyrA | 8588 | c.1287G>A | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 1.0 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8678 | c.1377G>A | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8696 | c.1395G>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8891 | c.1590G>A | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8933 | c.1632G>C | 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 | 8967 | p.Ala556Arg | missense_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 9104 | c.1803C>G | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9122 | c.1821C>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9152 | c.1851C>T | synonymous_variant | 1.0 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 1.0 |
| gyrA | 9158 | c.1857C>T | synonymous_variant | 1.0 |
| gyrA | 9161 | c.1860C>G | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9191 | c.1890G>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 1.0 |
| gyrA | 9224 | c.1923C>T | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>G | synonymous_variant | 1.0 |
| gyrA | 9239 | c.1938C>T | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_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 | 9300 | p.Ala667Ser | missense_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 1.0 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 1.0 |
| fgd1 | 490782 | c.-1G>C | upstream_gene_variant | 1.0 |
| fgd1 | 490797 | c.15G>A | synonymous_variant | 1.0 |
| fgd1 | 490800 | c.18A>C | synonymous_variant | 1.0 |
| fgd1 | 490803 | c.21T>A | synonymous_variant | 1.0 |
| fgd1 | 490812 | c.30A>G | synonymous_variant | 1.0 |
| fgd1 | 490815 | c.33G>C | synonymous_variant | 1.0 |
| fgd1 | 490827 | c.45C>T | synonymous_variant | 1.0 |
| fgd1 | 490848 | c.66A>G | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>T | synonymous_variant | 1.0 |
| fgd1 | 490868 | p.Ala29Gly | missense_variant | 1.0 |
| fgd1 | 490887 | c.105G>A | synonymous_variant | 1.0 |
| fgd1 | 490890 | c.108C>G | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 1.0 |
| fgd1 | 490911 | c.129T>G | synonymous_variant | 1.0 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Glu | missense_variant | 1.0 |
| fgd1 | 491001 | c.219G>C | synonymous_variant | 1.0 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 1.0 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 1.0 |
| fgd1 | 491043 | c.261T>G | 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 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| fgd1 | 491643 | c.861G>A | synonymous_variant | 1.0 |
| fgd1 | 491646 | c.864G>C | synonymous_variant | 1.0 |
| fgd1 | 491649 | c.867C>T | synonymous_variant | 1.0 |
| fgd1 | 491658 | c.876A>G | synonymous_variant | 1.0 |
| fgd1 | 491661 | c.879C>G | synonymous_variant | 1.0 |
| mshA | 575674 | c.327G>C | synonymous_variant | 1.0 |
| mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
| mshA | 575701 | c.354G>A | synonymous_variant | 1.0 |
| mshA | 575704 | c.357T>G | synonymous_variant | 1.0 |
| mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
| mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
| mshA | 575719 | c.372C>T | synonymous_variant | 1.0 |
| ccsA | 620196 | c.306C>G | synonymous_variant | 1.0 |
| ccsA | 620197 | p.Gln103Val | missense_variant | 1.0 |
| ccsA | 620226 | c.336G>A | synonymous_variant | 1.0 |
| ccsA | 620245 | c.355T>C | synonymous_variant | 1.0 |
| ccsA | 620249 | p.Ser120Cys | missense_variant | 1.0 |
| ccsA | 620254 | c.364_366delCTCinsTTG | synonymous_variant | 1.0 |
| ccsA | 620265 | c.375C>G | synonymous_variant | 1.0 |
| ccsA | 620340 | c.450C>G | synonymous_variant | 1.0 |
| ccsA | 620346 | c.456C>G | synonymous_variant | 1.0 |
| ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
| ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
| ccsA | 620373 | c.483C>T | synonymous_variant | 1.0 |
| ccsA | 620376 | c.486G>C | synonymous_variant | 1.0 |
| ccsA | 620385 | c.495G>C | synonymous_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620389 | c.499C>T | synonymous_variant | 1.0 |
| ccsA | 620412 | c.522T>C | synonymous_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620421 | c.531G>C | synonymous_variant | 1.0 |
| ccsA | 620424 | c.534G>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>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760370 | c.564C>G | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760380 | p.Thr192Leu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760472 | c.666C>T | 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 | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 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 | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760793 | c.987A>G | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
| rpoB | 760845 | p.Thr347Pro | missense_variant | 1.0 |
| rpoB | 760859 | c.1053T>C | synonymous_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760869 | p.Val355Ile | missense_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760931 | c.1125C>G | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>T | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>G | 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 | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761129 | c.1323G>C | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761213 | c.1407G>C | synonymous_variant | 1.0 |
| rpoB | 761219 | c.1413G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761306 | c.1500C>G | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761330 | c.1524G>C | synonymous_variant | 1.0 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
| rpoB | 761531 | c.1725C>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761588 | c.1782C>T | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761848 | p.Cys681Ser | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>C | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | 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 | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762206 | c.2400C>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762246 | c.2440C>T | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | 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 | 762395 | c.-975G>C | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
| rpoC | 762413 | c.-957G>A | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762419 | c.-951C>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762488 | c.-882G>C | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762521 | c.-849C>T | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | 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 | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763013 | c.-357C>G | 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 | 763067 | c.-303C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763158 | c.-212C>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763190 | c.-180C>T | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763227 | c.-143C>T | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763441 | c.72C>T | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763606 | c.237C>T | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763816 | c.447C>G | synonymous_variant | 1.0 |
| rpoC | 763853 | p.Val162Ile | missense_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
| rpoC | 763915 | c.546C>T | synonymous_variant | 1.0 |
| rpoC | 763942 | c.573C>G | synonymous_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 0.75 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 0.75 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764020 | c.651C>T | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 1.0 |
| rpoC | 764040 | p.Ser224Thr | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Ile | missense_variant | 1.0 |
| rpoC | 764112 | p.Tyr248Phe | missense_variant | 1.0 |
| rpoC | 764116 | c.747C>T | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ile | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764215 | c.846A>G | synonymous_variant | 1.0 |
| rpoC | 764236 | c.867G>A | synonymous_variant | 1.0 |
| rpoC | 764248 | c.879C>G | 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 | 764419 | c.1050C>G | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | 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 | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764489 | c.1120C>T | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
| rpoC | 764551 | c.1182G>C | synonymous_variant | 1.0 |
| rpoC | 764554 | c.1185C>T | 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 | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
| rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>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 | 765292 | c.1923G>C | synonymous_variant | 1.0 |
| rpoC | 765298 | c.1929G>C | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 1.0 |
| rpoC | 765326 | p.His653Ala | missense_variant | 1.0 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
| rpoC | 765346 | c.1977C>G | synonymous_variant | 1.0 |
| rpoC | 765349 | c.1980T>C | synonymous_variant | 1.0 |
| rpoC | 765352 | c.1983G>C | synonymous_variant | 1.0 |
| rpoC | 765364 | c.1995G>A | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 1.0 |
| rpoC | 765404 | p.Leu679Val | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 1.0 |
| rpoC | 765580 | c.2211G>C | synonymous_variant | 1.0 |
| rpoC | 765613 | p.His748Gln | missense_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>T | synonymous_variant | 1.0 |
| rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
| rpoC | 765753 | p.Asp795Ala | missense_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 | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766027 | c.2658G>C | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Glu | missense_variant | 1.0 |
| rpoC | 766054 | c.2685C>G | synonymous_variant | 1.0 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 1.0 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766357 | c.2988C>T | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766366 | c.2997C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>G | synonymous_variant | 1.0 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766462 | c.3093G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766522 | c.3153C>G | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
| rpoC | 766531 | c.3162G>C | synonymous_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766673 | p.Gly1102Asn | missense_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766795 | c.3426C>T | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>G | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767014 | c.3645G>C | synonymous_variant | 1.0 |
| rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>A | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 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 |
| mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.67 |
| mmpL5 | 775966 | p.Ala839Ser | missense_variant | 1.0 |
| mmpL5 | 775973 | c.2506_2508delTTGinsCTC | synonymous_variant | 0.67 |
| mmpL5 | 775981 | p.Leu834Met | missense_variant | 1.0 |
| mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.67 |
| mmpL5 | 775997 | c.2484T>C | synonymous_variant | 1.0 |
| mmpL5 | 776000 | p.Leu827Ile | missense_variant | 1.0 |
| mmpL5 | 776005 | p.Ile826Leu | missense_variant | 0.67 |
| mmpL5 | 776009 | c.2472A>G | synonymous_variant | 1.0 |
| mmpL5 | 776030 | c.2451G>A | synonymous_variant | 1.0 |
| mmpL5 | 776678 | c.1803G>C | synonymous_variant | 1.0 |
| mmpL5 | 776693 | p.Val596Ala | missense_variant | 1.0 |
| mmpL5 | 776705 | c.1776C>T | synonymous_variant | 1.0 |
| mmpL5 | 776729 | c.1752C>T | synonymous_variant | 1.0 |
| mmpL5 | 776738 | p.Ile581Met | missense_variant | 1.0 |
| mmpL5 | 776741 | c.1740C>G | synonymous_variant | 1.0 |
| mmpL5 | 776744 | c.1737C>G | synonymous_variant | 1.0 |
| mmpL5 | 777158 | c.1323C>G | synonymous_variant | 1.0 |
| mmpL5 | 777164 | c.1317C>G | synonymous_variant | 1.0 |
| mmpL5 | 777170 | c.1311T>C | synonymous_variant | 1.0 |
| mmpL5 | 777176 | p.Glu435Asp | missense_variant | 1.0 |
| mmpL5 | 777191 | c.1290C>G | synonymous_variant | 1.0 |
| mmpL5 | 777194 | c.1287A>G | synonymous_variant | 1.0 |
| mmpL5 | 777206 | c.1275A>G | synonymous_variant | 1.0 |
| mmpL5 | 777212 | p.Ala423Thr | missense_variant | 1.0 |
| mmpL5 | 777215 | c.1266C>G | synonymous_variant | 1.0 |
| mmpL5 | 777218 | c.1263G>A | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781605 | p.Ile16Val | missense_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
| rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781742 | c.183C>T | synonymous_variant | 1.0 |
| rpsL | 781748 | c.189C>G | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>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>C | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800627 | c.-182C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800794 | c.-15A>G | upstream_gene_variant | 1.0 |
| rplC | 800796 | c.-13A>G | upstream_gene_variant | 1.0 |
| rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 1.0 |
| rplC | 800814 | c.6A>G | synonymous_variant | 1.0 |
| rplC | 800817 | c.9A>T | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800874 | c.66A>G | synonymous_variant | 1.0 |
| rplC | 800875 | p.Val23Ile | missense_variant | 1.0 |
| rplC | 800880 | c.72A>G | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800892 | c.84G>C | synonymous_variant | 1.0 |
| rplC | 800907 | c.99C>G | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| rplC | 801367 | p.Ala187Thr | missense_variant | 1.0 |
| rplC | 801402 | c.594T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801426 | c.618C>G | synonymous_variant | 1.0 |
| rplC | 801427 | p.Met207Val | missense_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801442 | p.Ile212Val | missense_variant | 1.0 |
| fbiC | 1303530 | c.600G>A | synonymous_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
| fbiC | 1303539 | c.609G>C | synonymous_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303575 | c.645G>C | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303674 | c.744C>G | synonymous_variant | 1.0 |
| fbiC | 1303681 | c.751T>C | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | 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 | 1303728 | c.798G>A | synonymous_variant | 1.0 |
| fbiC | 1303731 | c.801A>C | synonymous_variant | 1.0 |
| fbiC | 1303732 | p.Ser268Ala | missense_variant | 1.0 |
| fbiC | 1303737 | c.807G>A | synonymous_variant | 1.0 |
| fbiC | 1303746 | c.816T>C | synonymous_variant | 1.0 |
| fbiC | 1303749 | c.819G>C | synonymous_variant | 1.0 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 1.0 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303836 | c.906G>C | synonymous_variant | 1.0 |
| fbiC | 1303845 | c.915C>G | synonymous_variant | 1.0 |
| fbiC | 1303846 | p.Phe306Val | missense_variant | 1.0 |
| fbiC | 1303854 | c.924T>C | synonymous_variant | 1.0 |
| fbiC | 1303860 | c.930A>C | synonymous_variant | 1.0 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 1.0 |
| fbiC | 1303905 | c.975G>C | synonymous_variant | 1.0 |
| fbiC | 1303909 | p.Pro327Ser | missense_variant | 1.0 |
| fbiC | 1303914 | c.984C>G | synonymous_variant | 1.0 |
| fbiC | 1303920 | c.990C>T | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>G | synonymous_variant | 1.0 |
| fbiC | 1304661 | c.1731C>T | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>C | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>G | synonymous_variant | 1.0 |
| fbiC | 1304808 | c.1878C>G | synonymous_variant | 1.0 |
| fbiC | 1304811 | c.1881C>G | synonymous_variant | 1.0 |
| fbiC | 1304817 | c.1887T>C | synonymous_variant | 1.0 |
| fbiC | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>T | synonymous_variant | 1.0 |
| fbiC | 1304853 | c.1923C>T | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304869 | c.1939C>T | synonymous_variant | 1.0 |
| fbiC | 1304875 | p.Ile649Val | missense_variant | 1.0 |
| fbiC | 1304883 | p.Glu651Asp | missense_variant | 1.0 |
| fbiC | 1304891 | p.Ile654Thr | missense_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304907 | c.1977C>G | synonymous_variant | 1.0 |
| fbiC | 1304910 | c.1980G>C | synonymous_variant | 1.0 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 1.0 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 1.0 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
| fbiC | 1305252 | c.2322G>A | synonymous_variant | 1.0 |
| fbiC | 1305273 | c.2343C>T | synonymous_variant | 1.0 |
| fbiC | 1305276 | c.2346G>C | synonymous_variant | 1.0 |
| fbiC | 1305279 | p.His783Gln | missense_variant | 1.0 |
| fbiC | 1305282 | c.2352T>C | synonymous_variant | 1.0 |
| fbiC | 1305318 | c.2388C>G | synonymous_variant | 1.0 |
| fbiC | 1305331 | p.Glu801Asn | missense_variant | 1.0 |
| fbiC | 1305336 | c.2406T>C | synonymous_variant | 1.0 |
| fbiC | 1305372 | c.2442G>A | synonymous_variant | 1.0 |
| fbiC | 1305384 | c.2454G>C | synonymous_variant | 1.0 |
| fbiC | 1305396 | c.2466C>G | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>G | synonymous_variant | 1.0 |
| fbiC | 1305417 | c.2487C>G | synonymous_variant | 1.0 |
| fbiC | 1305423 | c.2493T>C | synonymous_variant | 1.0 |
| fbiC | 1305430 | p.Val834Thr | missense_variant | 1.0 |
| atpE | 1460852 | c.-193C>G | upstream_gene_variant | 1.0 |
| atpE | 1460855 | c.-190T>C | upstream_gene_variant | 1.0 |
| atpE | 1460858 | c.-187C>G | upstream_gene_variant | 1.0 |
| atpE | 1460861 | c.-184C>G | upstream_gene_variant | 1.0 |
| atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461150 | p.Ile36Val | missense_variant | 1.0 |
| atpE | 1461158 | c.114T>G | synonymous_variant | 1.0 |
| atpE | 1461159 | p.Val39Ile | missense_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>T | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| atpE | 1461251 | c.207G>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| atpE | 1461275 | c.231T>A | synonymous_variant | 1.0 |
| rrs | 1471845 | n.-1G>T | upstream_gene_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472045 | n.200T>A | 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 | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | 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 | 1474639 | n.982G>A | 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 | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.89 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.88 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.9 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.9 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476048 | n.2391G>A | 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 | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476733 | n.3076C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476750 | n.3093T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673523 | c.-679G>T | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>G | upstream_gene_variant | 1.0 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673548 | p.Ala37Thr | missense_variant | 1.0 |
| inhA | 1673568 | c.-634C>G | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673580 | c.-622T>G | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 1.0 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673749 | p.Lys104Arg | missense_variant | 1.0 |
| fabG1 | 1673758 | p.Lys107Glu | missense_variant | 1.0 |
| fabG1 | 1673890 | p.Ala151Ser | missense_variant | 1.0 |
| inhA | 1673901 | c.-301A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673905 | p.Ser156Ala | missense_variant | 1.0 |
| inhA | 1673916 | c.-286A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673917 | p.Val160Leu | missense_variant | 1.0 |
| inhA | 1673922 | c.-280T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673941 | p.Ala168Ser | missense_variant | 1.0 |
| inhA | 1673946 | c.-256C>G | upstream_gene_variant | 1.0 |
| inhA | 1673955 | c.-247G>C | upstream_gene_variant | 1.0 |
| inhA | 1673961 | c.-241A>C | upstream_gene_variant | 1.0 |
| inhA | 1673985 | c.-217C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| inhA | 1674114 | c.-88T>A | upstream_gene_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>C | upstream_gene_variant | 1.0 |
| inhA | 1674132 | c.-70T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674136 | p.Ser233Ala | missense_variant | 1.0 |
| inhA | 1674141 | c.-61T>C | upstream_gene_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674552 | c.351C>G | synonymous_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674597 | c.396G>A | synonymous_variant | 1.0 |
| inhA | 1674601 | p.Leu134Thr | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674630 | c.429C>G | synonymous_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674672 | c.471C>G | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674708 | c.507G>A | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
| inhA | 1674789 | c.588G>C | synonymous_variant | 1.0 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 1.0 |
| inhA | 1674822 | c.621C>G | synonymous_variant | 1.0 |
| inhA | 1674828 | c.627G>A | synonymous_variant | 1.0 |
| inhA | 1674846 | p.Ile215Met | missense_variant | 1.0 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 1.0 |
| inhA | 1674900 | c.699G>A | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674909 | c.708G>A | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674960 | c.759C>G | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>G | synonymous_variant | 1.0 |
| rpsA | 1833532 | c.-10A>C | upstream_gene_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833940 | c.399C>G | synonymous_variant | 1.0 |
| rpsA | 1833971 | c.430C>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834096 | c.555G>C | synonymous_variant | 1.0 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>G | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>G | synonymous_variant | 1.0 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>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 | 1834303 | c.762T>C | 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 | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834510 | c.969C>T | synonymous_variant | 1.0 |
| rpsA | 1834513 | c.972C>G | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834654 | p.Glu371Asp | missense_variant | 1.0 |
| rpsA | 1834684 | c.1143C>T | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Ser | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834775 | p.Ala412Thr | 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 |
| tlyA | 1917975 | c.36C>G | synonymous_variant | 1.0 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 1.0 |
| tlyA | 1917990 | c.51G>C | synonymous_variant | 1.0 |
| tlyA | 1917993 | c.54A>G | synonymous_variant | 1.0 |
| tlyA | 1917996 | c.57A>G | synonymous_variant | 1.0 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 1.0 |
| ndh | 2101723 | c.1320G>C | synonymous_variant | 1.0 |
| ndh | 2101726 | c.1317A>C | synonymous_variant | 1.0 |
| ndh | 2101729 | c.1314G>C | synonymous_variant | 1.0 |
| ndh | 2101732 | c.1311T>C | synonymous_variant | 1.0 |
| ndh | 2101735 | c.1308A>G | synonymous_variant | 1.0 |
| ndh | 2101744 | p.Asp433Glu | missense_variant | 1.0 |
| ndh | 2101756 | c.1287G>C | synonymous_variant | 1.0 |
| ndh | 2101765 | c.1278C>G | synonymous_variant | 1.0 |
| ndh | 2101768 | c.1275C>A | synonymous_variant | 1.0 |
| ndh | 2101771 | c.1272T>G | synonymous_variant | 1.0 |
| ndh | 2101774 | c.1269T>C | synonymous_variant | 1.0 |
| ndh | 2101777 | c.1266C>G | synonymous_variant | 1.0 |
| ndh | 2101783 | c.1260T>A | synonymous_variant | 1.0 |
| ndh | 2101804 | c.1239T>G | synonymous_variant | 1.0 |
| ndh | 2101808 | p.Thr412Ser | missense_variant | 1.0 |
| ndh | 2101830 | p.Ile405Val | missense_variant | 1.0 |
| ndh | 2101912 | c.1131G>C | synonymous_variant | 1.0 |
| ndh | 2101920 | c.1123A>C | synonymous_variant | 1.0 |
| ndh | 2101924 | c.1119T>G | synonymous_variant | 1.0 |
| ndh | 2101939 | c.1104A>G | synonymous_variant | 1.0 |
| ndh | 2101960 | c.1083A>G | synonymous_variant | 1.0 |
| ndh | 2101963 | c.1080G>A | synonymous_variant | 1.0 |
| ndh | 2101966 | c.1077T>G | synonymous_variant | 1.0 |
| ndh | 2101972 | c.1071G>C | synonymous_variant | 1.0 |
| ndh | 2101988 | p.Ala352Asp | missense_variant | 1.0 |
| ndh | 2101990 | c.1053G>C | synonymous_variant | 1.0 |
| ndh | 2101993 | c.1050A>G | synonymous_variant | 1.0 |
| ndh | 2102011 | c.1032C>G | synonymous_variant | 1.0 |
| ndh | 2102014 | c.1029C>G | synonymous_variant | 1.0 |
| ndh | 2102710 | c.333C>T | synonymous_variant | 1.0 |
| katG | 2155677 | c.435C>G | synonymous_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
| katG | 2155704 | c.408C>G | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155740 | p.Gly124Gln | missense_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155794 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155836 | c.276C>G | synonymous_variant | 1.0 |
| pncA | 2289913 | c.-672T>C | upstream_gene_variant | 1.0 |
| pncA | 2289925 | c.-684T>C | upstream_gene_variant | 1.0 |
| pncA | 2289930 | c.-689A>G | upstream_gene_variant | 1.0 |
| pncA | 2289936 | c.-695T>G | upstream_gene_variant | 0.5 |
| pncA | 2289943 | c.-702T>G | upstream_gene_variant | 1.0 |
| pncA | 2289948 | c.-707C>T | upstream_gene_variant | 1.0 |
| pncA | 2289949 | c.-708A>G | upstream_gene_variant | 1.0 |
| pncA | 2289987 | c.-746C>T | upstream_gene_variant | 1.0 |
| pncA | 2289991 | c.-750G>C | upstream_gene_variant | 1.0 |
| pncA | 2289994 | c.-753A>G | upstream_gene_variant | 1.0 |
| pncA | 2289997 | c.-756G>C | upstream_gene_variant | 1.0 |
| pncA | 2290009 | c.-768A>G | upstream_gene_variant | 1.0 |
| pncA | 2290015 | c.-774A>C | upstream_gene_variant | 1.0 |
| kasA | 2517950 | c.-165C>G | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2517993 | c.-122G>T | upstream_gene_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 1.0 |
| kasA | 2518199 | p.Ile29Val | missense_variant | 1.0 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 1.0 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518261 | p.Glu49Asp | missense_variant | 1.0 |
| kasA | 2518263 | p.Phe50Tyr | missense_variant | 1.0 |
| kasA | 2518265 | p.Val51Ile | missense_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
| kasA | 2518528 | c.414C>G | synonymous_variant | 1.0 |
| kasA | 2518540 | c.426T>C | synonymous_variant | 1.0 |
| kasA | 2518657 | c.543G>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518702 | c.588C>T | synonymous_variant | 1.0 |
| kasA | 2518705 | c.591T>C | synonymous_variant | 1.0 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518744 | c.630C>T | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>T | synonymous_variant | 1.0 |
| kasA | 2518777 | c.663C>T | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518789 | c.675G>C | synonymous_variant | 1.0 |
| kasA | 2518792 | c.678C>A | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2519050 | c.936C>G | synonymous_variant | 1.0 |
| kasA | 2519053 | c.939G>C | synonymous_variant | 1.0 |
| kasA | 2519056 | c.942G>C | synonymous_variant | 1.0 |
| kasA | 2519062 | c.948T>G | synonymous_variant | 1.0 |
| kasA | 2519068 | c.954C>T | synonymous_variant | 1.0 |
| kasA | 2519072 | p.Ala320Thr | missense_variant | 1.0 |
| kasA | 2519107 | c.993T>C | synonymous_variant | 1.0 |
| kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
| kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
| kasA | 2519137 | c.1023T>G | synonymous_variant | 1.0 |
| kasA | 2519158 | c.1044C>T | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>G | synonymous_variant | 1.0 |
| kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
| kasA | 2519196 | p.Thr361Ser | missense_variant | 1.0 |
| kasA | 2519215 | c.1101C>T | synonymous_variant | 1.0 |
| kasA | 2519218 | c.1104G>A | synonymous_variant | 1.0 |
| kasA | 2519221 | c.1107G>C | synonymous_variant | 1.0 |
| kasA | 2519227 | c.1113G>C | synonymous_variant | 1.0 |
| kasA | 2519230 | c.1116C>T | synonymous_variant | 1.0 |
| kasA | 2519236 | c.1122G>A | synonymous_variant | 1.0 |
| kasA | 2519239 | c.1125A>C | synonymous_variant | 1.0 |
| kasA | 2519245 | c.1131T>C | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | p.Asp159Glu | missense_variant | 1.0 |
| ahpC | 2726672 | c.480G>A | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>C | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| folC | 2746414 | p.Glu395Gln | missense_variant | 1.0 |
| folC | 2746420 | c.1179A>C | synonymous_variant | 1.0 |
| folC | 2746426 | c.1173G>C | synonymous_variant | 1.0 |
| folC | 2746438 | c.1161G>C | synonymous_variant | 1.0 |
| folC | 2746451 | p.Gly383Ala | missense_variant | 1.0 |
| folC | 2746471 | c.1128C>A | synonymous_variant | 1.0 |
| folC | 2746478 | p.Phe374Tyr | missense_variant | 1.0 |
| folC | 2747021 | p.Val193Ala | missense_variant | 1.0 |
| folC | 2747023 | c.576C>G | synonymous_variant | 1.0 |
| folC | 2747026 | c.573C>G | synonymous_variant | 1.0 |
| folC | 2747032 | c.567A>C | synonymous_variant | 1.0 |
| folC | 2747059 | c.540T>C | synonymous_variant | 1.0 |
| folC | 2747062 | c.537A>G | synonymous_variant | 1.0 |
| folC | 2747065 | c.534C>T | synonymous_variant | 1.0 |
| folC | 2747248 | c.351G>C | synonymous_variant | 1.0 |
| folC | 2747264 | p.Gly112Ala | missense_variant | 1.0 |
| folC | 2747266 | c.333C>T | synonymous_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747289 | p.Pro104Ala | missense_variant | 1.0 |
| folC | 2747290 | c.309A>G | synonymous_variant | 1.0 |
| folC | 2747293 | c.306G>A | synonymous_variant | 1.0 |
| folC | 2747302 | c.297A>G | synonymous_variant | 1.0 |
| folC | 2747314 | c.285A>C | synonymous_variant | 1.0 |
| folC | 2747317 | c.282C>G | synonymous_variant | 1.0 |
| folC | 2747343 | p.Val86Ile | missense_variant | 1.0 |
| folC | 2747355 | p.Val82Ile | missense_variant | 1.0 |
| folC | 2747359 | c.240C>G | synonymous_variant | 1.0 |
| folC | 2747362 | c.237G>C | synonymous_variant | 1.0 |
| folC | 2747394 | p.Ile69Val | missense_variant | 1.0 |
| folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
| folC | 2747407 | c.192T>C | synonymous_variant | 1.0 |
| folC | 2747410 | c.187_188delAG | frameshift_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747422 | c.177G>A | synonymous_variant | 1.0 |
| folC | 2747425 | c.174C>T | synonymous_variant | 1.0 |
| folC | 2747442 | c.157T>C | synonymous_variant | 1.0 |
| ribD | 2987066 | c.228A>G | synonymous_variant | 1.0 |
| ribD | 2987069 | c.231T>C | synonymous_variant | 1.0 |
| ribD | 2987092 | p.Val85Ala | missense_variant | 1.0 |
| ribD | 2987105 | c.267C>G | synonymous_variant | 1.0 |
| ribD | 2987108 | c.270T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 1.0 |
| Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065007 | c.1185G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065249 | c.943T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065268 | c.924A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 1.0 |
| Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066351 | c.-160G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066357 | c.-166G>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 1.0 |
| Rv2752c | 3066369 | c.-180_-178delAGCinsGCG | upstream_gene_variant | 1.0 |
| Rv2752c | 3066380 | c.-189A>G | upstream_gene_variant | 1.0 |
| thyX | 3067313 | c.633G>T | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067349 | c.597G>C | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067367 | c.579G>C | synonymous_variant | 1.0 |
| thyX | 3067373 | c.573C>G | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067442 | c.504C>T | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067462 | c.484C>T | synonymous_variant | 1.0 |
| thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067490 | c.456C>G | synonymous_variant | 1.0 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
| thyX | 3067545 | p.Glu134Ala | missense_variant | 1.0 |
| thyX | 3067549 | p.Thr133Ala | missense_variant | 1.0 |
| thyX | 3067556 | p.His130Gln | missense_variant | 1.0 |
| thyX | 3067559 | c.387C>G | synonymous_variant | 1.0 |
| thyX | 3067565 | p.Asp127Glu | missense_variant | 1.0 |
| thyX | 3067570 | p.Ala126Pro | missense_variant | 1.0 |
| thyX | 3067577 | c.369G>A | synonymous_variant | 1.0 |
| thyX | 3067601 | p.Arg115His | missense_variant | 1.0 |
| thyX | 3067611 | p.Lys112Thr | missense_variant | 1.0 |
| thyX | 3067619 | c.327A>C | synonymous_variant | 1.0 |
| thyX | 3067631 | c.315C>G | synonymous_variant | 1.0 |
| thyX | 3067634 | c.312C>G | synonymous_variant | 1.0 |
| thyX | 3067637 | c.309G>A | synonymous_variant | 1.0 |
| thyX | 3067652 | c.294T>C | synonymous_variant | 1.0 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>C | synonymous_variant | 1.0 |
| thyX | 3067691 | p.Ile85Leu | missense_variant | 1.0 |
| thyX | 3067694 | c.252G>C | synonymous_variant | 1.0 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyX | 3067736 | c.210C>T | synonymous_variant | 1.0 |
| thyA | 3073812 | c.660C>G | synonymous_variant | 1.0 |
| thyA | 3073815 | c.657G>A | synonymous_variant | 1.0 |
| thyA | 3073824 | c.648A>G | synonymous_variant | 1.0 |
| thyA | 3073827 | c.645A>G | synonymous_variant | 1.0 |
| thyA | 3073839 | c.633T>C | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>G | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073866 | c.606C>G | synonymous_variant | 1.0 |
| thyA | 3073872 | p.Ile200Val | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073898 | p.Ala192Ser | missense_variant | 1.0 |
| thyA | 3073917 | c.555C>G | synonymous_variant | 1.0 |
| ald | 3087680 | c.861G>C | synonymous_variant | 1.0 |
| ald | 3087704 | c.885T>C | synonymous_variant | 1.0 |
| ald | 3087716 | c.897G>C | synonymous_variant | 1.0 |
| fprA | 3473809 | c.-198G>C | upstream_gene_variant | 1.0 |
| fprA | 3473812 | c.-195G>A | upstream_gene_variant | 1.0 |
| fprA | 3475056 | c.1050C>G | synonymous_variant | 1.0 |
| fprA | 3475061 | p.Pro352Arg | missense_variant | 1.0 |
| fprA | 3475074 | c.1068C>G | synonymous_variant | 1.0 |
| fprA | 3475104 | c.1098G>C | synonymous_variant | 1.0 |
| fprA | 3475107 | c.1101G>C | synonymous_variant | 1.0 |
| fprA | 3475113 | c.1107G>C | synonymous_variant | 1.0 |
| fprA | 3475129 | p.Ala375Ser | missense_variant | 1.0 |
| fprA | 3475134 | c.1128A>G | synonymous_variant | 1.0 |
| fprA | 3475143 | c.1137C>G | synonymous_variant | 1.0 |
| fbiA | 3640347 | c.-196A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640349 | c.-194A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640350 | c.-193C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641914 | p.Ala127Gly | missense_variant | 1.0 |
| fbiB | 3641924 | c.390A>C | synonymous_variant | 1.0 |
| fbiB | 3641927 | c.393C>G | synonymous_variant | 1.0 |
| fbiB | 3641928 | c.394T>C | synonymous_variant | 1.0 |
| fbiB | 3641938 | p.Gly135Ala | missense_variant | 1.0 |
| fbiB | 3641961 | p.Thr143Glu | missense_variant | 1.0 |
| fbiB | 3641972 | c.438G>C | synonymous_variant | 1.0 |
| fbiB | 3642617 | c.1083C>G | synonymous_variant | 1.0 |
| fbiB | 3642620 | c.1086T>C | synonymous_variant | 1.0 |
| fbiB | 3642656 | c.1122G>C | synonymous_variant | 1.0 |
| fbiB | 3642659 | c.1125C>G | synonymous_variant | 1.0 |
| fbiB | 3642668 | c.1134A>G | synonymous_variant | 1.0 |
| fbiB | 3642677 | c.1143A>G | synonymous_variant | 1.0 |
| fbiB | 3642680 | c.1146A>G | synonymous_variant | 1.0 |
| fbiB | 3642684 | c.1150T>C | synonymous_variant | 1.0 |
| fbiB | 3642701 | c.1167C>G | synonymous_variant | 1.0 |
| fbiB | 3642719 | c.1185T>C | synonymous_variant | 1.0 |
| fbiB | 3642731 | c.1197C>G | synonymous_variant | 1.0 |
| fbiB | 3642743 | c.1209T>C | synonymous_variant | 1.0 |
| fbiB | 3642749 | c.1215T>C | synonymous_variant | 1.0 |
| fbiB | 3642758 | c.1224C>G | synonymous_variant | 1.0 |
| fbiB | 3642763 | p.Asp410Ala | missense_variant | 1.0 |
| fbiB | 3642770 | c.1236G>C | synonymous_variant | 1.0 |
| fbiB | 3642779 | c.1245A>C | synonymous_variant | 1.0 |
| fbiB | 3642781 | p.Val416Ala | missense_variant | 1.0 |
| rpoA | 3877515 | c.993G>C | synonymous_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 1.0 |
| rpoA | 3877571 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877679 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
| rpoA | 3877890 | c.618C>T | synonymous_variant | 1.0 |
| rpoA | 3877896 | c.612G>C | synonymous_variant | 1.0 |
| rpoA | 3877900 | p.Ser203Asn | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877909 | p.Asn200Ser | missense_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877986 | c.522G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878040 | c.468T>C | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.83 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878304 | c.204G>C | synonymous_variant | 1.0 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878376 | c.132G>C | synonymous_variant | 1.0 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 1.0 |
| rpoA | 3878388 | c.120C>G | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>C | synonymous_variant | 1.0 |
| rpoA | 3878415 | c.93C>T | synonymous_variant | 1.0 |
| rpoA | 3878424 | c.84G>C | synonymous_variant | 1.0 |
| rpoA | 3878436 | c.72A>G | synonymous_variant | 1.0 |
| rpoA | 3878442 | c.66G>C | synonymous_variant | 1.0 |
| rpoA | 3878454 | c.54A>C | synonymous_variant | 1.0 |
| rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
| rpoA | 3878478 | c.30C>G | synonymous_variant | 1.0 |
| rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 1.0 |
| clpC1 | 4038433 | c.2272C>T | synonymous_variant | 1.0 |
| clpC1 | 4038434 | c.2271G>A | synonymous_variant | 1.0 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
| clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
| clpC1 | 4038460 | p.Leu749Met | missense_variant | 1.0 |
| clpC1 | 4038486 | p.Gly740Asn | missense_variant | 1.0 |
| clpC1 | 4038489 | p.Ala739Gly | missense_variant | 1.0 |
| clpC1 | 4038494 | c.2211G>C | synonymous_variant | 1.0 |
| clpC1 | 4038497 | p.Ser736Gln | missense_variant | 1.0 |
| clpC1 | 4038509 | c.2196C>T | synonymous_variant | 1.0 |
| clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
| clpC1 | 4038541 | c.2164C>T | synonymous_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>G | synonymous_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038749 | c.1956C>G | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>G | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039186 | c.1519C>T | synonymous_variant | 1.0 |
| clpC1 | 4039349 | c.1356C>T | synonymous_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>G | synonymous_variant | 1.0 |
| clpC1 | 4039364 | c.1341C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>T | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039576 | p.Ala377Pro | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>G | synonymous_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
| clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040201 | c.504C>G | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040318 | c.387C>G | synonymous_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>T | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040477 | c.228G>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>G | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040528 | c.177G>C | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| clpC1 | 4040695 | c.10C>A | synonymous_variant | 1.0 |
| clpC1 | 4040699 | c.6C>T | synonymous_variant | 1.0 |
| clpC1 | 4040706 | c.-4_-3delAC | upstream_gene_variant | 1.0 |
| clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4040728 | c.-24G>T | upstream_gene_variant | 1.0 |
| panD | 4044072 | c.210C>G | synonymous_variant | 1.0 |
| panD | 4044075 | c.207T>C | synonymous_variant | 1.0 |
| panD | 4044081 | c.201T>C | synonymous_variant | 1.0 |
| panD | 4044084 | c.198T>C | synonymous_variant | 1.0 |
| panD | 4044105 | c.177G>C | synonymous_variant | 1.0 |
| panD | 4044117 | c.165G>C | synonymous_variant | 1.0 |
| panD | 4044120 | c.162A>C | synonymous_variant | 1.0 |
| panD | 4044123 | c.159T>C | synonymous_variant | 1.0 |
| panD | 4044126 | c.156T>C | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044150 | c.132A>G | synonymous_variant | 1.0 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240819 | c.957A>G | synonymous_variant | 1.0 |
| embC | 4240828 | c.966G>A | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4241032 | c.1170G>C | synonymous_variant | 1.0 |
| embC | 4241038 | c.1176G>C | synonymous_variant | 1.0 |
| embC | 4241047 | c.1185C>G | synonymous_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241053 | c.1191G>C | synonymous_variant | 1.0 |
| embC | 4241089 | c.1227C>G | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241146 | c.1284C>G | synonymous_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 | 4241170 | c.1308G>C | synonymous_variant | 1.0 |
| embC | 4241173 | c.1311C>T | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241479 | c.1617C>G | synonymous_variant | 1.0 |
| embC | 4241480 | c.1618T>C | synonymous_variant | 1.0 |
| embC | 4241488 | c.1626G>C | synonymous_variant | 1.0 |
| embC | 4241496 | p.Ala545Gly | missense_variant | 1.0 |
| embC | 4241500 | c.1638A>C | synonymous_variant | 1.0 |
| embC | 4241501 | p.Ser547Thr | missense_variant | 1.0 |
| embC | 4241506 | c.1644G>C | synonymous_variant | 1.0 |
| embC | 4241518 | c.1656A>G | synonymous_variant | 1.0 |
| embC | 4241521 | c.1659T>C | synonymous_variant | 1.0 |
| embC | 4241530 | c.1668C>G | synonymous_variant | 1.0 |
| embC | 4241536 | c.1674A>G | synonymous_variant | 1.0 |
| embC | 4241539 | c.1677T>C | synonymous_variant | 1.0 |
| embC | 4241545 | c.1683T>C | synonymous_variant | 1.0 |
| embC | 4241548 | c.1686T>C | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>G | synonymous_variant | 1.0 |
| embC | 4241567 | p.Ile569Val | missense_variant | 1.0 |
| embC | 4241572 | c.1710C>G | synonymous_variant | 1.0 |
| embC | 4241578 | c.1716G>C | synonymous_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241591 | p.Leu577Val | missense_variant | 1.0 |
| embC | 4241611 | c.1749G>C | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embC | 4241626 | c.1764T>C | synonymous_variant | 1.0 |
| embC | 4241635 | c.1773G>C | synonymous_variant | 1.0 |
| embC | 4241719 | c.1857G>C | synonymous_variant | 1.0 |
| embC | 4241727 | p.Phe622Tyr | missense_variant | 1.0 |
| embC | 4241741 | p.Val627Leu | missense_variant | 1.0 |
| embC | 4241747 | p.Val629Leu | missense_variant | 1.0 |
| embC | 4241750 | p.Leu630Val | missense_variant | 1.0 |
| embC | 4241755 | c.1893C>G | synonymous_variant | 1.0 |
| embC | 4241770 | c.1908T>C | synonymous_variant | 1.0 |
| embC | 4241791 | c.1929G>C | synonymous_variant | 1.0 |
| embC | 4241794 | c.1932C>G | synonymous_variant | 1.0 |
| embC | 4241797 | c.1935C>T | synonymous_variant | 1.0 |
| embC | 4241809 | c.1947A>C | synonymous_variant | 1.0 |
| embC | 4242710 | p.Gln950Glu | missense_variant | 1.0 |
| embA | 4242715 | c.-518T>C | upstream_gene_variant | 1.0 |
| embA | 4242742 | c.-491C>G | upstream_gene_variant | 1.0 |
| embA | 4242748 | c.-485A>G | upstream_gene_variant | 1.0 |
| embA | 4242754 | c.-479G>C | upstream_gene_variant | 1.0 |
| embC | 4242764 | p.Val968Leu | missense_variant | 1.0 |
| embA | 4242772 | c.-461G>C | upstream_gene_variant | 1.0 |
| embC | 4242779 | p.Asn973Asp | missense_variant | 1.0 |
| embA | 4244516 | c.1284G>C | synonymous_variant | 1.0 |
| embA | 4244517 | p.Leu429Val | missense_variant | 1.0 |
| embA | 4244523 | p.Pro431Ala | missense_variant | 1.0 |
| embA | 4244534 | c.1302T>C | synonymous_variant | 1.0 |
| embA | 4244537 | c.1305T>G | synonymous_variant | 1.0 |
| embA | 4244543 | c.1311C>G | synonymous_variant | 1.0 |
| embA | 4244547 | p.Ile439Val | missense_variant | 1.0 |
| embA | 4244557 | p.Arg442Thr | missense_variant | 1.0 |
| embA | 4244582 | c.1350T>C | synonymous_variant | 1.0 |
| embA | 4244585 | c.1353A>G | synonymous_variant | 1.0 |
| embA | 4244611 | p.Ala460Gly | missense_variant | 1.0 |
| embA | 4244616 | p.Ala462Ser | missense_variant | 1.0 |
| embA | 4244619 | c.1387_1389delTTGinsCTC | synonymous_variant | 1.0 |
| embA | 4244625 | p.Leu465Val | missense_variant | 1.0 |
| embA | 4244631 | p.Thr467Leu | missense_variant | 1.0 |
| embA | 4245041 | c.1809C>G | synonymous_variant | 1.0 |
| embA | 4245044 | c.1812G>C | synonymous_variant | 1.0 |
| embA | 4245053 | c.1821G>C | synonymous_variant | 1.0 |
| embA | 4245060 | c.1828T>C | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245089 | c.1857G>C | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245137 | c.1905T>C | synonymous_variant | 1.0 |
| embA | 4245146 | c.1914G>A | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245153 | p.Ile641Val | missense_variant | 1.0 |
| embA | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245189 | c.1957C>T | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Ile | missense_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>C | synonymous_variant | 1.0 |
| embA | 4245222 | p.Tyr664Gln | missense_variant | 1.0 |
| embA | 4245248 | c.2016G>C | synonymous_variant | 1.0 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 1.0 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 1.0 |
| embA | 4245282 | p.Ile684Val | missense_variant | 1.0 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245290 | c.2058C>G | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>G | synonymous_variant | 1.0 |
| embA | 4245296 | c.2064G>C | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 1.0 |
| embB | 4245674 | c.-840A>C | upstream_gene_variant | 1.0 |
| embB | 4245677 | c.-837G>C | upstream_gene_variant | 1.0 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245701 | c.-813G>C | upstream_gene_variant | 1.0 |
| embB | 4245704 | c.-810G>C | upstream_gene_variant | 1.0 |
| embB | 4245725 | c.-789A>G | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788T>C | upstream_gene_variant | 1.0 |
| embB | 4245737 | c.-777A>C | upstream_gene_variant | 1.0 |
| embB | 4245740 | c.-774T>C | upstream_gene_variant | 1.0 |
| embB | 4245785 | c.-729G>C | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245812 | c.-702G>C | upstream_gene_variant | 1.0 |
| embA | 4245813 | p.Pro861Ala | missense_variant | 1.0 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 1.0 |
| embB | 4245824 | c.-690G>C | upstream_gene_variant | 1.0 |
| embB | 4245833 | c.-681G>C | upstream_gene_variant | 1.0 |
| embB | 4245842 | c.-672G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>C | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embB | 4245860 | c.-654C>G | upstream_gene_variant | 1.0 |
| embA | 4245885 | p.Asp885Thr | missense_variant | 1.0 |
| embA | 4245892 | p.Ile887Thr | missense_variant | 1.0 |
| embB | 4245899 | c.-615C>G | upstream_gene_variant | 1.0 |
| embB | 4245902 | c.-612G>A | upstream_gene_variant | 1.0 |
| embB | 4245905 | c.-609C>G | upstream_gene_variant | 1.0 |
| embB | 4245911 | c.-603A>G | upstream_gene_variant | 1.0 |
| embB | 4245917 | c.-597G>A | upstream_gene_variant | 1.0 |
| embA | 4245930 | p.Gly900Arg | missense_variant | 1.0 |
| embB | 4246211 | c.-303T>C | upstream_gene_variant | 1.0 |
| embB | 4246217 | c.-297G>A | upstream_gene_variant | 1.0 |
| embB | 4246220 | c.-294T>C | upstream_gene_variant | 1.0 |
| embB | 4246223 | c.-291C>T | upstream_gene_variant | 1.0 |
| embA | 4246227 | p.Ile999Val | missense_variant | 1.0 |
| embB | 4246235 | c.-279G>A | upstream_gene_variant | 1.0 |
| embA | 4246242 | p.Gln1004Gly | missense_variant | 1.0 |
| embB | 4246250 | c.-264G>C | upstream_gene_variant | 1.0 |
| embB | 4246256 | c.-258G>T | upstream_gene_variant | 1.0 |
| embB | 4246259 | c.-255G>C | upstream_gene_variant | 1.0 |
| embA | 4246264 | p.His1011Arg | missense_variant | 1.0 |
| embB | 4246292 | c.-222A>G | upstream_gene_variant | 1.0 |
| embA | 4246305 | p.Ser1025Glu | missense_variant | 1.0 |
| embA | 4246308 | p.Thr1026Ala | missense_variant | 1.0 |
| embB | 4246316 | c.-198T>G | upstream_gene_variant | 1.0 |
| embB | 4246319 | c.-195G>C | upstream_gene_variant | 1.0 |
| embA | 4246329 | p.Thr1033Ala | missense_variant | 1.0 |
| embB | 4246349 | c.-165C>G | upstream_gene_variant | 1.0 |
| embA | 4246359 | p.Ala1043Ser | missense_variant | 1.0 |
| embB | 4246367 | c.-147C>T | upstream_gene_variant | 1.0 |
| embB | 4246373 | c.-141T>C | upstream_gene_variant | 1.0 |
| embB | 4246376 | c.-138G>C | upstream_gene_variant | 1.0 |
| embB | 4246379 | c.-135C>T | upstream_gene_variant | 1.0 |
| embB | 4246400 | c.-114G>C | upstream_gene_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247425 | c.912G>C | synonymous_variant | 1.0 |
| embB | 4247434 | c.921C>G | 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 | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247566 | c.1053C>A | synonymous_variant | 1.0 |
| embB | 4247572 | c.1059A>G | synonymous_variant | 1.0 |
| embB | 4247746 | c.1233C>T | synonymous_variant | 1.0 |
| embB | 4247761 | c.1248T>C | synonymous_variant | 1.0 |
| embB | 4247773 | c.1260G>A | synonymous_variant | 1.0 |
| embB | 4247776 | c.1263G>T | synonymous_variant | 1.0 |
| embB | 4247797 | c.1284C>G | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>T | synonymous_variant | 1.0 |
| embB | 4247803 | c.1290G>C | synonymous_variant | 1.0 |
| embB | 4247815 | c.1302C>G | synonymous_variant | 1.0 |
| embB | 4247819 | p.Val436Ile | missense_variant | 1.0 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 1.0 |
| embB | 4247836 | c.1323A>G | synonymous_variant | 1.0 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 1.0 |
| embB | 4247866 | c.1353G>C | synonymous_variant | 1.0 |
| embB | 4247875 | c.1362G>C | synonymous_variant | 1.0 |
| embB | 4247876 | c.1363C>T | synonymous_variant | 1.0 |
| embB | 4247881 | c.1368G>C | synonymous_variant | 1.0 |
| embB | 4247887 | c.1374C>T | synonymous_variant | 1.0 |
| embB | 4247893 | c.1380C>T | synonymous_variant | 1.0 |
| embB | 4247899 | p.Met462Ile | missense_variant | 1.0 |
| embB | 4247905 | c.1392G>C | synonymous_variant | 1.0 |
| embB | 4247909 | c.1396T>C | synonymous_variant | 1.0 |
| embB | 4247914 | c.1401G>C | synonymous_variant | 1.0 |
| embB | 4247956 | c.1443G>C | synonymous_variant | 1.0 |
| embB | 4247974 | c.1461C>G | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 1.0 |
| embB | 4248011 | p.Ser500Arg | missense_variant | 1.0 |
| embB | 4248014 | p.Thr501Ala | missense_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248040 | c.1527C>G | synonymous_variant | 1.0 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248097 | c.1584C>G | synonymous_variant | 1.0 |
| embB | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248172 | c.1659G>C | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248200 | p.Ile563Val | missense_variant | 1.0 |
| embB | 4248205 | c.1692C>G | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>C | synonymous_variant | 1.0 |
| embB | 4248304 | c.1791G>C | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249423 | p.Asp970Glu | missense_variant | 1.0 |
| embB | 4249424 | p.Leu971Met | missense_variant | 1.0 |
| embB | 4249429 | c.2916C>T | synonymous_variant | 1.0 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 1.0 |
| embB | 4249441 | c.2928A>G | synonymous_variant | 1.0 |
| embB | 4249444 | c.2931T>C | synonymous_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 1.0 |
| aftB | 4267580 | c.1257G>T | synonymous_variant | 1.0 |
| aftB | 4267604 | c.1233C>G | synonymous_variant | 1.0 |
| aftB | 4267607 | c.1230G>A | synonymous_variant | 1.0 |
| aftB | 4267622 | c.1215G>C | synonymous_variant | 1.0 |
| aftB | 4267625 | c.1212T>C | synonymous_variant | 1.0 |
| aftB | 4267628 | c.1209C>G | synonymous_variant | 1.0 |
| aftB | 4267634 | p.Arg401His | missense_variant | 1.0 |
| aftB | 4268066 | p.Val257Leu | missense_variant | 1.0 |
| aftB | 4268081 | c.756A>G | synonymous_variant | 1.0 |
| aftB | 4268084 | c.753G>C | synonymous_variant | 1.0 |
| aftB | 4268096 | c.741C>G | synonymous_variant | 1.0 |
| aftB | 4268099 | c.738G>C | synonymous_variant | 1.0 |
| aftB | 4268102 | c.735C>G | synonymous_variant | 1.0 |
| aftB | 4268117 | c.720G>C | synonymous_variant | 1.0 |
| aftB | 4268123 | p.Ser238Gly | missense_variant | 1.0 |
| aftB | 4268129 | c.708T>G | synonymous_variant | 1.0 |
| aftB | 4268138 | c.699A>C | synonymous_variant | 1.0 |
| aftB | 4268144 | c.693T>C | synonymous_variant | 1.0 |
| aftB | 4269206 | c.-370C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269220 | p.Ala205Lys | missense_variant | 1.0 |
| aftB | 4269222 | c.-386T>C | upstream_gene_variant | 1.0 |
| aftB | 4269242 | c.-406C>T | upstream_gene_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| aftB | 4269249 | c.-413G>A | upstream_gene_variant | 1.0 |
| ubiA | 4269521 | p.Val105Leu | missense_variant | 1.0 |
| ubiA | 4269524 | p.Thr104Ala | missense_variant | 1.0 |
| aftB | 4269528 | c.-692G>C | upstream_gene_variant | 1.0 |
| aftB | 4269549 | c.-713C>G | upstream_gene_variant | 1.0 |
| aftB | 4269552 | c.-716C>G | upstream_gene_variant | 1.0 |
| aftB | 4269555 | c.-719C>G | upstream_gene_variant | 1.0 |
| aftB | 4269564 | c.-728G>C | upstream_gene_variant | 1.0 |
