Run ID: SRR6832249
Sample name:
Date: 04-04-2023 17:19:09
Number of reads: 1959954
Percentage reads mapped: 80.62
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.98 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.97 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.2 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5287 | c.48T>C | synonymous_variant | 0.15 |
gyrB | 5293 | c.54C>G | synonymous_variant | 0.17 |
gyrB | 5302 | c.63A>G | synonymous_variant | 0.17 |
gyrB | 5305 | c.66G>A | synonymous_variant | 0.16 |
gyrB | 5308 | c.69G>A | synonymous_variant | 0.15 |
gyrB | 5341 | c.102T>C | synonymous_variant | 0.15 |
gyrB | 5527 | c.288C>G | synonymous_variant | 0.15 |
gyrA | 7090 | c.-212C>T | upstream_gene_variant | 0.16 |
gyrA | 7093 | c.-209T>C | upstream_gene_variant | 0.15 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.15 |
gyrA | 7108 | c.-194G>A | upstream_gene_variant | 0.15 |
gyrA | 7120 | c.-182T>C | upstream_gene_variant | 0.17 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.14 |
gyrA | 7766 | c.465C>T | synonymous_variant | 0.19 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.18 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.17 |
gyrA | 7787 | c.486G>A | synonymous_variant | 0.17 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.18 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.17 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.17 |
gyrA | 7838 | c.537C>T | synonymous_variant | 0.17 |
gyrA | 7850 | c.549C>G | synonymous_variant | 0.14 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.14 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.16 |
gyrA | 8315 | c.1014G>A | synonymous_variant | 0.15 |
gyrA | 8318 | c.1017C>G | synonymous_variant | 0.17 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.2 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.17 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.17 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.16 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.14 |
gyrA | 8433 | p.Thr378Arg | missense_variant | 0.14 |
gyrA | 8447 | c.1146C>A | synonymous_variant | 0.14 |
gyrA | 8450 | c.1149G>A | synonymous_variant | 0.14 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.14 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.14 |
gyrA | 8561 | c.1260A>G | synonymous_variant | 0.17 |
gyrA | 8571 | c.1270C>T | synonymous_variant | 0.17 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.19 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.18 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.2 |
gyrA | 8627 | c.1326C>T | synonymous_variant | 0.2 |
gyrA | 8633 | c.1332C>G | synonymous_variant | 0.2 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.2 |
gyrA | 8655 | p.Ile452Val | missense_variant | 0.21 |
gyrA | 8666 | c.1365G>C | synonymous_variant | 0.19 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.16 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.22 |
gyrA | 8723 | c.1422G>A | synonymous_variant | 0.17 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.15 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.15 |
gyrA | 9003 | c.1702C>T | synonymous_variant | 0.16 |
gyrA | 9017 | c.1716C>T | synonymous_variant | 0.15 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.13 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.15 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.16 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9476 | c.2175G>C | synonymous_variant | 0.15 |
gyrA | 9479 | c.2178G>T | synonymous_variant | 0.16 |
gyrA | 9485 | c.2184A>C | synonymous_variant | 0.15 |
gyrA | 9488 | c.2187G>C | synonymous_variant | 0.14 |
gyrA | 9494 | c.2193T>C | synonymous_variant | 0.14 |
gyrA | 9497 | c.2196G>C | synonymous_variant | 0.14 |
gyrA | 9503 | c.2202T>C | synonymous_variant | 0.15 |
gyrA | 9518 | c.2217A>G | synonymous_variant | 0.15 |
gyrA | 9527 | c.2226A>G | synonymous_variant | 0.13 |
fgd1 | 490863 | c.81C>A | synonymous_variant | 0.14 |
fgd1 | 490869 | c.87C>T | synonymous_variant | 0.16 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.18 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.17 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.17 |
fgd1 | 490911 | c.129T>C | synonymous_variant | 0.17 |
fgd1 | 490921 | p.Gln47Lys | missense_variant | 0.14 |
fgd1 | 490929 | c.147C>G | synonymous_variant | 0.15 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.16 |
fgd1 | 490935 | c.153C>G | synonymous_variant | 0.16 |
fgd1 | 490945 | c.163C>T | synonymous_variant | 0.16 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.16 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.16 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.21 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.24 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.22 |
fgd1 | 491067 | c.285C>T | synonymous_variant | 0.23 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.26 |
fgd1 | 491085 | c.303T>G | synonymous_variant | 0.25 |
fgd1 | 491091 | c.309T>G | synonymous_variant | 0.24 |
fgd1 | 491094 | c.312C>T | synonymous_variant | 0.24 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.3 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.27 |
fgd1 | 491142 | c.360C>G | synonymous_variant | 0.23 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.18 |
fgd1 | 491154 | p.Glu124Asp | missense_variant | 0.17 |
fgd1 | 491163 | c.381G>A | synonymous_variant | 0.15 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.15 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.18 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.17 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575629 | c.282A>T | synonymous_variant | 0.14 |
mshA | 575633 | p.Ala96Thr | missense_variant | 0.15 |
mshA | 575652 | p.Arg102Gln | missense_variant | 0.16 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.16 |
mshA | 575662 | c.315C>A | synonymous_variant | 0.17 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.16 |
mshA | 575686 | c.339G>A | synonymous_variant | 0.17 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.19 |
mshA | 575692 | c.345G>A | synonymous_variant | 0.17 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.18 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.17 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.98 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.14 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759635 | c.-172C>T | upstream_gene_variant | 0.19 |
rpoB | 759644 | c.-163T>A | upstream_gene_variant | 0.19 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.2 |
rpoB | 759661 | c.-146G>C | upstream_gene_variant | 0.15 |
rpoB | 759671 | c.-136G>T | upstream_gene_variant | 0.14 |
rpoB | 760059 | p.Tyr85Asp | missense_variant | 0.14 |
rpoB | 760067 | c.261G>C | synonymous_variant | 0.15 |
rpoB | 760070 | c.264T>A | synonymous_variant | 0.15 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.15 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.16 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.16 |
rpoB | 760118 | c.312T>C | synonymous_variant | 0.16 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.16 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.19 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.18 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.17 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.17 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.18 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.16 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.14 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.19 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.18 |
rpoB | 760859 | c.1053T>G | synonymous_variant | 0.18 |
rpoB | 760868 | c.1062C>G | synonymous_variant | 0.17 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.15 |
rpoB | 760920 | c.1114C>T | synonymous_variant | 0.16 |
rpoB | 760971 | c.1165C>A | synonymous_variant | 0.14 |
rpoB | 760994 | c.1188G>A | synonymous_variant | 0.23 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.29 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.3 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.33 |
rpoB | 761036 | c.1230G>A | synonymous_variant | 0.31 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.31 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.29 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.28 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.14 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.16 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.32 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.29 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.3 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.31 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.24 |
rpoB | 761300 | c.1494G>A | synonymous_variant | 0.23 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.17 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.18 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.16 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.16 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.15 |
rpoB | 761600 | c.1794T>G | synonymous_variant | 0.14 |
rpoB | 761603 | c.1797C>T | synonymous_variant | 0.13 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.14 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.16 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.13 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.16 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.16 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.16 |
rpoB | 762020 | c.2214G>A | synonymous_variant | 0.15 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.15 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.17 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.15 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.14 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.16 |
rpoB | 762224 | c.2418C>G | synonymous_variant | 0.18 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.19 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.17 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.17 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.18 |
rpoC | 763076 | c.-294C>T | upstream_gene_variant | 0.18 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.18 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.19 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763124 | c.-246C>T | upstream_gene_variant | 0.14 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.14 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.19 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.19 |
rpoC | 763430 | c.61A>C | synonymous_variant | 0.18 |
rpoC | 763435 | c.66A>G | synonymous_variant | 0.2 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.22 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.21 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.23 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.3 |
rpoC | 763505 | c.136C>T | synonymous_variant | 0.31 |
rpoC | 763561 | c.192G>A | synonymous_variant | 0.26 |
rpoC | 763600 | c.231C>T | synonymous_variant | 0.23 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.23 |
rpoC | 763618 | c.249C>A | synonymous_variant | 0.19 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.16 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.17 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.15 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.15 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.16 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.14 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.14 |
rpoC | 764272 | c.903G>T | synonymous_variant | 0.15 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.15 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.15 |
rpoC | 764317 | c.948C>T | synonymous_variant | 0.2 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.24 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.24 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.2 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.18 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.18 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.17 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.16 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.17 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.18 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.13 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.14 |
rpoC | 764536 | c.1167G>A | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.18 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.17 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.17 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.14 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.14 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.13 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.14 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.16 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.16 |
rpoC | 765395 | c.2026C>T | synonymous_variant | 0.14 |
rpoC | 765405 | p.Leu679Pro | missense_variant | 0.15 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.15 |
rpoC | 765430 | c.2061G>A | synonymous_variant | 0.15 |
rpoC | 765445 | c.2076G>T | synonymous_variant | 0.21 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.17 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.16 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.26 |
rpoC | 765496 | c.2127C>G | synonymous_variant | 0.31 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.29 |
rpoC | 765526 | c.2157C>G | synonymous_variant | 0.27 |
rpoC | 765541 | c.2172C>A | synonymous_variant | 0.24 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.23 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.28 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.28 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.28 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.23 |
rpoC | 765586 | c.2217G>A | synonymous_variant | 0.22 |
rpoC | 765589 | c.2220G>C | synonymous_variant | 0.26 |
rpoC | 765610 | c.2241C>T | synonymous_variant | 0.24 |
rpoC | 765612 | p.His748Arg | missense_variant | 0.19 |
rpoC | 765622 | p.Glu751Asp | missense_variant | 0.23 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.2 |
rpoC | 765724 | c.2355C>G | synonymous_variant | 0.14 |
rpoC | 765727 | c.2358T>C | synonymous_variant | 0.14 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.18 |
rpoC | 765752 | p.Asp795Ser | missense_variant | 0.15 |
rpoC | 765757 | c.2388C>T | synonymous_variant | 0.15 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.16 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.15 |
rpoC | 765790 | c.2421C>T | synonymous_variant | 0.15 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.15 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.16 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.17 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.17 |
rpoC | 765826 | c.2457T>A | synonymous_variant | 0.14 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.14 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.14 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.14 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.15 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.19 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.17 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.18 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.18 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.17 |
rpoC | 765997 | c.2628T>C | synonymous_variant | 0.16 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.14 |
rpoC | 766324 | c.2955C>T | synonymous_variant | 0.2 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.26 |
rpoC | 766360 | c.2991C>T | synonymous_variant | 0.26 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.2 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.2 |
rpoC | 766387 | c.3018C>G | synonymous_variant | 0.2 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.21 |
rpoC | 766397 | c.3028C>T | synonymous_variant | 0.21 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.23 |
rpoC | 766417 | c.3048C>T | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.17 |
rpoC | 766519 | c.3150C>A | synonymous_variant | 0.15 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.14 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.14 |
rpoC | 766537 | c.3168G>A | synonymous_variant | 0.15 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.15 |
rpoC | 766570 | c.3201T>G | synonymous_variant | 0.15 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.15 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.2 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.2 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.18 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.21 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.23 |
rpoC | 766621 | c.3252G>A | synonymous_variant | 0.17 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.18 |
rpoC | 766654 | c.3285C>G | synonymous_variant | 0.17 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.16 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.15 |
rpoC | 766700 | c.3331C>T | synonymous_variant | 0.17 |
rpoC | 766714 | c.3345G>C | synonymous_variant | 0.21 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.16 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.18 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.14 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.19 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.19 |
rpoC | 766795 | c.3426C>T | synonymous_variant | 0.19 |
rpoC | 766801 | c.3432C>T | synonymous_variant | 0.17 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.21 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.26 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.22 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.22 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.24 |
rpoC | 766903 | c.3534C>T | synonymous_variant | 0.24 |
rpoC | 766907 | c.3538C>T | synonymous_variant | 0.26 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.27 |
rpoC | 766921 | c.3552G>C | synonymous_variant | 0.28 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.31 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.29 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.31 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.32 |
rpoC | 766975 | c.3606C>T | synonymous_variant | 0.32 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.4 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.42 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.4 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.24 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.23 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.19 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.16 |
rpoC | 767206 | c.3837C>A | synonymous_variant | 0.14 |
rpoC | 767209 | c.3840T>G | synonymous_variant | 0.16 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.13 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.14 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.14 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.16 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.15 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.14 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.14 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.16 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.13 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.15 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.17 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.23 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.24 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.24 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.26 |
rplC | 800913 | c.105G>C | synonymous_variant | 0.25 |
rplC | 800916 | c.108A>T | synonymous_variant | 0.22 |
rplC | 800922 | c.114C>G | synonymous_variant | 0.2 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.24 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.24 |
rplC | 800946 | c.138T>G | synonymous_variant | 0.21 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.2 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.18 |
rplC | 800958 | c.150G>A | synonymous_variant | 0.18 |
fbiC | 1303503 | c.573G>C | synonymous_variant | 0.22 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.19 |
fbiC | 1303512 | c.582T>G | synonymous_variant | 0.2 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.22 |
fbiC | 1303551 | c.621G>C | synonymous_variant | 0.24 |
fbiC | 1303578 | c.648G>A | synonymous_variant | 0.21 |
fbiC | 1303584 | c.654C>A | synonymous_variant | 0.23 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.16 |
fbiC | 1303591 | c.661C>A | synonymous_variant | 0.16 |
fbiC | 1303594 | c.664C>T | synonymous_variant | 0.16 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.13 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.14 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.14 |
fbiC | 1304074 | p.Ala382Ser | missense_variant | 0.14 |
fbiC | 1304079 | c.1149A>G | synonymous_variant | 0.15 |
fbiC | 1304091 | c.1161C>T | synonymous_variant | 0.17 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.17 |
fbiC | 1304112 | c.1182G>A | synonymous_variant | 0.23 |
fbiC | 1304127 | c.1197A>G | synonymous_variant | 0.14 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.21 |
fbiC | 1304163 | c.1233G>C | synonymous_variant | 0.19 |
fbiC | 1304164 | p.Gly412Arg | missense_variant | 0.19 |
fbiC | 1304172 | c.1242G>T | synonymous_variant | 0.19 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.19 |
fbiC | 1304178 | c.1248G>C | synonymous_variant | 0.18 |
fbiC | 1304181 | c.1251G>T | synonymous_variant | 0.18 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.19 |
fbiC | 1304200 | p.Leu424Phe | missense_variant | 0.18 |
fbiC | 1304205 | c.1275C>G | synonymous_variant | 0.19 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.19 |
fbiC | 1304217 | p.Asn429Lys | missense_variant | 0.15 |
fbiC | 1304511 | c.1581C>T | synonymous_variant | 0.2 |
fbiC | 1304523 | c.1593G>A | synonymous_variant | 0.14 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.14 |
fbiC | 1304546 | p.Val539Ala | missense_variant | 0.19 |
fbiC | 1304556 | c.1626C>T | synonymous_variant | 0.35 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.33 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.3 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.3 |
fbiC | 1304598 | c.1668C>T | synonymous_variant | 0.35 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.3 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.31 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.29 |
fbiC | 1304649 | c.1719C>T | synonymous_variant | 0.21 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.15 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.15 |
fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.18 |
fbiC | 1304679 | c.1749G>A | synonymous_variant | 0.19 |
fbiC | 1304715 | c.1785G>T | synonymous_variant | 0.17 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.14 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.15 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.16 |
fbiC | 1304751 | c.1821C>G | synonymous_variant | 0.21 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.17 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 0.24 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.25 |
fbiC | 1304790 | c.1860C>A | synonymous_variant | 0.24 |
fbiC | 1304799 | c.1869G>C | synonymous_variant | 0.24 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.19 |
fbiC | 1304809 | p.Ser627Glu | missense_variant | 0.19 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.17 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.16 |
fbiC | 1305126 | c.2196T>C | synonymous_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473600 | n.-58A>G | upstream_gene_variant | 0.15 |
rrl | 1473603 | n.-55C>T | upstream_gene_variant | 0.16 |
rrl | 1473607 | n.-50_-49delGG | upstream_gene_variant | 0.16 |
rrl | 1473626 | n.-32_-31insT | upstream_gene_variant | 0.15 |
rrl | 1473648 | n.-9_-7delTTG | upstream_gene_variant | 0.22 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475369 | n.1712G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.13 |
inhA | 1673535 | c.-667A>G | upstream_gene_variant | 0.18 |
inhA | 1673547 | c.-655T>C | upstream_gene_variant | 0.18 |
inhA | 1673568 | c.-634C>G | upstream_gene_variant | 0.21 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.15 |
inhA | 1673589 | c.-613A>C | upstream_gene_variant | 0.13 |
fabG1 | 1673596 | p.Lys53Glu | missense_variant | 0.13 |
inhA | 1673736 | c.-466G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673767 | p.Asn110Asp | missense_variant | 0.13 |
inhA | 1673946 | c.-256C>A | upstream_gene_variant | 0.17 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.18 |
fabG1 | 1673960 | p.Ala174Val | missense_variant | 0.17 |
inhA | 1673970 | c.-232C>G | upstream_gene_variant | 0.14 |
inhA | 1673976 | c.-226T>C | upstream_gene_variant | 0.14 |
inhA | 1673982 | c.-220G>C | upstream_gene_variant | 0.14 |
inhA | 1673988 | c.-214G>C | upstream_gene_variant | 0.14 |
inhA | 1673991 | c.-211C>G | upstream_gene_variant | 0.14 |
inhA | 1674675 | c.474C>T | synonymous_variant | 0.13 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.15 |
inhA | 1674852 | c.651G>A | synonymous_variant | 0.14 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.17 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.13 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.13 |
inhA | 1674912 | c.711G>C | synonymous_variant | 0.17 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.14 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 0.14 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.16 |
rpsA | 1833718 | c.177C>T | synonymous_variant | 0.17 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.19 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.16 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.19 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.19 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.22 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.22 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.18 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.17 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.17 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.2 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.22 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.16 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.2 |
rpsA | 1834024 | c.483G>A | synonymous_variant | 0.24 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.24 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.18 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.18 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.17 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.17 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.16 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.19 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.17 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.15 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.13 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101912 | c.1131G>C | synonymous_variant | 0.16 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.2 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.19 |
ndh | 2101936 | c.1107G>C | synonymous_variant | 0.18 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.17 |
ndh | 2101960 | c.1083A>C | synonymous_variant | 0.14 |
ndh | 2101963 | c.1080G>A | synonymous_variant | 0.15 |
ndh | 2102908 | c.135C>T | synonymous_variant | 0.14 |
ndh | 2102911 | c.132G>C | synonymous_variant | 0.18 |
ndh | 2102919 | c.124C>T | synonymous_variant | 0.18 |
ndh | 2102929 | c.114T>C | synonymous_variant | 0.17 |
ndh | 2102932 | c.111C>T | synonymous_variant | 0.16 |
ndh | 2102938 | c.105G>T | synonymous_variant | 0.19 |
ndh | 2102962 | c.81A>C | synonymous_variant | 0.2 |
ndh | 2102965 | c.78G>C | synonymous_variant | 0.2 |
ndh | 2102974 | c.69G>A | synonymous_variant | 0.17 |
ndh | 2102989 | c.54G>C | synonymous_variant | 0.18 |
ndh | 2102992 | c.51T>C | synonymous_variant | 0.19 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.97 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.16 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.16 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.22 |
katG | 2155649 | p.Tyr155His | missense_variant | 0.24 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.18 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.17 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.16 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.16 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.96 |
PPE35 | 2169221 | c.1392T>C | synonymous_variant | 1.0 |
PPE35 | 2170623 | c.-11G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.23 |
kasA | 2517956 | c.-159G>A | upstream_gene_variant | 0.22 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.2 |
kasA | 2518681 | c.567C>T | synonymous_variant | 0.13 |
kasA | 2518684 | c.570C>A | synonymous_variant | 0.13 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.25 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.22 |
kasA | 2518735 | c.621C>A | synonymous_variant | 0.21 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.18 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.15 |
kasA | 2518756 | c.642G>C | synonymous_variant | 0.14 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.16 |
kasA | 2518789 | c.675G>T | synonymous_variant | 0.15 |
kasA | 2518798 | c.684G>C | synonymous_variant | 0.15 |
kasA | 2518816 | c.702C>T | synonymous_variant | 0.18 |
kasA | 2518822 | c.708C>T | synonymous_variant | 0.18 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.18 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.15 |
kasA | 2518856 | p.Ile248Leu | missense_variant | 0.15 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.14 |
eis | 2714955 | c.378C>T | synonymous_variant | 1.0 |
eis | 2715123 | c.210G>T | synonymous_variant | 1.0 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 0.15 |
folC | 2746663 | c.936T>C | synonymous_variant | 0.14 |
pepQ | 2859438 | c.981T>C | synonymous_variant | 0.14 |
pepQ | 2859468 | c.951G>T | synonymous_variant | 0.19 |
pepQ | 2859489 | p.Val310Ala | missense_variant | 0.22 |
pepQ | 2859510 | c.909T>C | synonymous_variant | 0.19 |
pepQ | 2859528 | c.891T>C | synonymous_variant | 0.18 |
pepQ | 2859540 | c.879A>T | synonymous_variant | 0.14 |
Rv2752c | 3065556 | c.636G>A | synonymous_variant | 0.22 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.21 |
Rv2752c | 3065583 | c.609G>C | synonymous_variant | 0.22 |
Rv2752c | 3065594 | c.598C>T | synonymous_variant | 0.19 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.19 |
Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 0.19 |
Rv2752c | 3065625 | c.567G>C | synonymous_variant | 0.19 |
Rv2752c | 3065634 | c.558G>C | synonymous_variant | 0.18 |
Rv2752c | 3065637 | c.555A>G | synonymous_variant | 0.16 |
Rv2752c | 3065640 | c.552T>C | synonymous_variant | 0.16 |
Rv2752c | 3065652 | c.540C>A | synonymous_variant | 0.14 |
Rv2752c | 3065675 | p.Phe173Leu | missense_variant | 0.13 |
thyX | 3067295 | c.651C>T | synonymous_variant | 0.13 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.14 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.27 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.23 |
thyX | 3067331 | c.615C>T | synonymous_variant | 0.21 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.16 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.23 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.19 |
thyX | 3067394 | c.552G>T | synonymous_variant | 0.19 |
thyX | 3067406 | c.540A>G | synonymous_variant | 0.2 |
thyX | 3067445 | c.501C>A | synonymous_variant | 0.17 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.14 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.13 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.16 |
thyX | 3067784 | c.162C>T | synonymous_variant | 0.16 |
thyX | 3067787 | p.Lys53Arg | missense_variant | 0.16 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.16 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.23 |
thyX | 3067817 | c.129C>T | synonymous_variant | 0.23 |
thyX | 3067820 | c.126C>G | synonymous_variant | 0.22 |
thyX | 3067832 | c.114C>T | synonymous_variant | 0.23 |
thyX | 3067838 | c.108C>G | synonymous_variant | 0.2 |
thyX | 3067847 | p.Pro33Ser | missense_variant | 0.17 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.14 |
thyA | 3073947 | c.525G>C | synonymous_variant | 0.17 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.15 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.23 |
thyA | 3073997 | c.475C>T | synonymous_variant | 0.23 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.2 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.26 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.22 |
thyA | 3074045 | c.427C>T | synonymous_variant | 0.22 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.21 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.23 |
thyA | 3074061 | p.Glu137Asp | missense_variant | 0.22 |
thyA | 3074091 | c.381C>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.87 |
fbiA | 3640562 | p.Ala7Val | missense_variant | 0.2 |
fbiB | 3640587 | c.-948C>T | upstream_gene_variant | 0.14 |
fbiB | 3640591 | c.-944_-942delCTCinsTTG | upstream_gene_variant | 0.14 |
fbiB | 3640606 | c.-929C>T | upstream_gene_variant | 0.15 |
fbiB | 3640620 | c.-915C>A | upstream_gene_variant | 0.14 |
fbiB | 3641948 | c.414G>A | synonymous_variant | 0.15 |
rpoA | 3877602 | c.906C>T | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.14 |
rpoA | 3877620 | c.888G>A | synonymous_variant | 0.15 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.14 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.17 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.2 |
rpoA | 3877737 | c.771G>T | synonymous_variant | 0.2 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.18 |
rpoA | 3877746 | c.762G>C | synonymous_variant | 0.17 |
rpoA | 3877752 | c.756C>T | synonymous_variant | 0.16 |
rpoA | 3877755 | c.753C>A | synonymous_variant | 0.16 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.15 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.21 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.21 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.15 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.17 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.15 |
rpoA | 3877886 | c.622C>T | synonymous_variant | 0.14 |
rpoA | 3877950 | c.558C>T | synonymous_variant | 0.18 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.2 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.14 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.17 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.18 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.15 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.16 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.16 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.17 |
rpoA | 3878043 | c.465G>T | synonymous_variant | 0.21 |
rpoA | 3878058 | c.450G>C | synonymous_variant | 0.16 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.19 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.16 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.15 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.18 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.2 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.15 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.2 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.17 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.17 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.18 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.16 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.16 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.16 |
rpoA | 3878376 | c.132G>A | synonymous_variant | 0.16 |
rpoA | 3878381 | c.127C>T | synonymous_variant | 0.16 |
rpoA | 3878391 | c.117T>A | synonymous_variant | 0.15 |
rpoA | 3878512 | c.-6_-5insGAA | upstream_gene_variant | 0.22 |
ddn | 3986954 | c.111G>C | synonymous_variant | 0.13 |
ddn | 3986957 | c.114C>T | synonymous_variant | 0.14 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.17 |
clpC1 | 4038272 | c.2433T>C | synonymous_variant | 0.17 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.17 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.17 |
clpC1 | 4038308 | c.2397G>C | synonymous_variant | 0.15 |
clpC1 | 4038314 | c.2391T>G | synonymous_variant | 0.18 |
clpC1 | 4038335 | c.2370C>T | synonymous_variant | 0.17 |
clpC1 | 4038344 | c.2361G>A | synonymous_variant | 0.2 |
clpC1 | 4038383 | c.2322G>A | synonymous_variant | 0.17 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.17 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.17 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.16 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.15 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.17 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.14 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.13 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.14 |
clpC1 | 4038695 | c.2010C>A | synonymous_variant | 0.14 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.21 |
clpC1 | 4038800 | c.1905C>T | synonymous_variant | 0.26 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.27 |
clpC1 | 4038838 | c.1867C>T | synonymous_variant | 0.34 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.33 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.31 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.19 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.16 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.24 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.21 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.21 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.19 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.21 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.19 |
clpC1 | 4038995 | c.1710G>A | synonymous_variant | 0.19 |
clpC1 | 4039009 | c.1696C>T | synonymous_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.15 |
clpC1 | 4039442 | c.1261_1263delCTAinsTTG | synonymous_variant | 0.16 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.15 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.15 |
clpC1 | 4039601 | c.1104G>C | synonymous_variant | 0.14 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.13 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.13 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.19 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039868 | c.837C>T | synonymous_variant | 0.14 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.14 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.18 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.19 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.24 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.21 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.26 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.23 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.28 |
clpC1 | 4040091 | c.613_614delTCinsAG | synonymous_variant | 0.34 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.34 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.39 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.3 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.27 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.29 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.21 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.17 |
clpC1 | 4040594 | c.111G>T | synonymous_variant | 0.15 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.14 |
clpC1 | 4040600 | c.105A>G | synonymous_variant | 0.14 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.14 |
clpC1 | 4040636 | c.69C>G | synonymous_variant | 0.17 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.18 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.16 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.13 |
embC | 4240484 | p.Ala208Thr | missense_variant | 0.14 |
embC | 4240489 | c.627A>G | synonymous_variant | 0.13 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.13 |
embC | 4240512 | p.Ser217Thr | missense_variant | 0.15 |
embC | 4240516 | c.654G>C | synonymous_variant | 0.15 |
embC | 4240519 | c.657T>C | synonymous_variant | 0.14 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.13 |
embC | 4240699 | c.837C>A | synonymous_variant | 0.16 |
embC | 4240717 | c.855T>C | synonymous_variant | 0.17 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.18 |
embC | 4240741 | c.879C>T | synonymous_variant | 0.21 |
embC | 4240777 | c.915G>A | synonymous_variant | 0.25 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.24 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.24 |
embC | 4240795 | c.933C>G | synonymous_variant | 0.23 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.24 |
embC | 4240831 | c.969T>C | synonymous_variant | 0.29 |
embC | 4240858 | c.996G>A | synonymous_variant | 0.18 |
embC | 4240859 | p.Leu333Met | missense_variant | 0.16 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.15 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.14 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.15 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.14 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.16 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.19 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.16 |
embC | 4241153 | p.Ile431Leu | missense_variant | 0.23 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.19 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.18 |
embC | 4241167 | c.1305C>G | synonymous_variant | 0.17 |
embC | 4241197 | c.1335G>C | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242740 | p.Leu960Phe | missense_variant | 0.14 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244170 | p.Gln313Arg | missense_variant | 0.14 |
embA | 4244178 | p.Ala316Ser | missense_variant | 0.14 |
embA | 4244260 | p.Val343Ala | missense_variant | 0.14 |
embA | 4244283 | p.Pro351Lys | missense_variant | 0.21 |
embA | 4244291 | c.1059G>C | synonymous_variant | 0.22 |
embA | 4244856 | p.Ala542Pro | missense_variant | 0.24 |
embA | 4244885 | c.1653A>G | synonymous_variant | 0.29 |
embA | 4244897 | c.1665T>G | synonymous_variant | 0.23 |
embA | 4244903 | c.1671G>C | synonymous_variant | 0.22 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.14 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.14 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.2 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.18 |
embA | 4245186 | p.Thr652Ala | missense_variant | 0.18 |
embA | 4245224 | c.1992T>C | synonymous_variant | 0.14 |
embB | 4245674 | c.-840A>T | upstream_gene_variant | 0.14 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.16 |
embB | 4246013 | c.-501T>C | upstream_gene_variant | 0.14 |
embA | 4246020 | p.Ala930Thr | missense_variant | 0.16 |
embB | 4246028 | c.-486G>C | upstream_gene_variant | 0.17 |
embB | 4246070 | c.-444G>C | upstream_gene_variant | 0.21 |
embB | 4246082 | c.-432T>C | upstream_gene_variant | 0.17 |
embB | 4246115 | c.-399T>C | upstream_gene_variant | 0.13 |
embB | 4246172 | c.-342C>T | upstream_gene_variant | 0.2 |
embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.19 |
embB | 4246244 | c.-270G>A | upstream_gene_variant | 0.14 |
embA | 4246254 | p.Leu1008Met | missense_variant | 0.24 |
embB | 4246259 | c.-255G>C | upstream_gene_variant | 0.24 |
embB | 4246265 | c.-249C>T | upstream_gene_variant | 0.21 |
embB | 4246268 | c.-246G>A | upstream_gene_variant | 0.21 |
embA | 4246279 | p.Ala1016Val | missense_variant | 0.23 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.27 |
embB | 4246307 | c.-207G>C | upstream_gene_variant | 0.31 |
embB | 4246316 | c.-198T>C | upstream_gene_variant | 0.28 |
embB | 4246346 | c.-168C>G | upstream_gene_variant | 0.26 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.16 |
embB | 4247348 | p.Thr279Leu | missense_variant | 0.14 |
embB | 4247353 | c.840C>T | synonymous_variant | 0.14 |
embB | 4247355 | p.Ala281Gly | missense_variant | 0.14 |
embB | 4247365 | c.852A>C | synonymous_variant | 0.16 |
embB | 4247370 | p.Gly286Ala | missense_variant | 0.17 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.19 |
embB | 4247398 | c.885G>C | synonymous_variant | 0.23 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.23 |
embB | 4247404 | c.891G>C | synonymous_variant | 0.23 |
embB | 4247407 | c.894G>C | synonymous_variant | 0.23 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.22 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.14 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.15 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.15 |
embB | 4247555 | p.Leu348Ile | missense_variant | 0.14 |
embB | 4247566 | c.1053C>G | synonymous_variant | 0.16 |
embB | 4247579 | p.Ala356Phe | missense_variant | 0.16 |
embB | 4247590 | c.1077A>G | synonymous_variant | 0.16 |
embB | 4247611 | c.1098G>C | synonymous_variant | 0.13 |
embB | 4247722 | c.1209G>C | synonymous_variant | 0.14 |
embB | 4247725 | c.1212G>C | synonymous_variant | 0.14 |
embB | 4247743 | c.1230C>G | synonymous_variant | 0.14 |
embB | 4247779 | c.1266C>G | synonymous_variant | 0.14 |
embB | 4247785 | c.1272G>C | synonymous_variant | 0.14 |
embB | 4247800 | c.1287A>C | synonymous_variant | 0.14 |
embB | 4248407 | p.Leu632Val | missense_variant | 0.13 |
embB | 4249429 | c.2916C>G | synonymous_variant | 0.14 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.13 |
embB | 4249492 | c.2979C>G | synonymous_variant | 0.13 |
embB | 4249501 | c.2988C>T | synonymous_variant | 0.17 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.16 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.14 |
embB | 4249540 | c.3027C>T | synonymous_variant | 0.14 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.15 |
embB | 4249675 | c.3162C>G | synonymous_variant | 0.13 |
embB | 4249693 | c.3180T>C | synonymous_variant | 0.18 |
embB | 4249699 | c.3186T>A | synonymous_variant | 0.19 |
embB | 4249702 | c.3189C>A | synonymous_variant | 0.2 |
embB | 4249703 | c.3190C>T | synonymous_variant | 0.2 |
embB | 4249711 | c.3198G>A | synonymous_variant | 0.2 |
embB | 4249735 | c.3222T>G | synonymous_variant | 0.14 |
embB | 4249741 | c.3228C>A | synonymous_variant | 0.15 |
embB | 4249750 | p.Glu1079Asp | missense_variant | 0.13 |
aftB | 4267529 | c.1308T>C | synonymous_variant | 0.13 |
aftB | 4267535 | c.1302A>G | synonymous_variant | 0.13 |
aftB | 4267556 | c.1281G>C | synonymous_variant | 0.14 |
aftB | 4267574 | c.1263G>C | synonymous_variant | 0.18 |
aftB | 4267580 | c.1257G>A | synonymous_variant | 0.19 |
aftB | 4267592 | c.1245C>G | synonymous_variant | 0.2 |
aftB | 4267622 | c.1215G>C | synonymous_variant | 0.14 |
aftB | 4267635 | p.Arg401Gln | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.88 |
aftB | 4267856 | c.981T>C | synonymous_variant | 0.2 |
aftB | 4267879 | p.Val320Leu | missense_variant | 0.14 |
aftB | 4267891 | p.Val316Ile | missense_variant | 0.17 |
aftB | 4267892 | p.Ile315Met | missense_variant | 0.17 |
aftB | 4267898 | c.939T>C | synonymous_variant | 0.19 |
aftB | 4268978 | c.-142C>T | upstream_gene_variant | 0.17 |
aftB | 4268994 | c.-158T>C | upstream_gene_variant | 0.24 |
aftB | 4269000 | c.-164G>A | upstream_gene_variant | 0.21 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.21 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.2 |
aftB | 4269027 | c.-191C>G | upstream_gene_variant | 0.21 |
aftB | 4269030 | c.-194C>G | upstream_gene_variant | 0.22 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.22 |
aftB | 4269045 | c.-209G>C | upstream_gene_variant | 0.2 |
aftB | 4269660 | c.-824C>A | upstream_gene_variant | 0.15 |
ubiA | 4269663 | p.Met57Val | missense_variant | 0.15 |
aftB | 4269669 | c.-833G>T | upstream_gene_variant | 0.18 |
ubiA | 4269676 | p.Ser53Thr | missense_variant | 0.2 |
aftB | 4269678 | c.-842C>G | upstream_gene_variant | 0.21 |
ubiA | 4269688 | p.Val49Ala | missense_variant | 0.22 |
aftB | 4269690 | c.-854C>T | upstream_gene_variant | 0.23 |
aftB | 4269699 | c.-863C>A | upstream_gene_variant | 0.23 |
aftB | 4269705 | c.-869T>C | upstream_gene_variant | 0.23 |
ubiA | 4269710 | p.Gly42Arg | missense_variant | 0.21 |
ubiA | 4269715 | p.Leu40Ala | missense_variant | 0.19 |
aftB | 4269723 | c.-887G>C | upstream_gene_variant | 0.19 |
ethA | 4326346 | c.1128C>G | synonymous_variant | 0.15 |
ethA | 4326352 | c.1122T>G | synonymous_variant | 0.17 |
ethA | 4326535 | c.939G>C | synonymous_variant | 0.14 |
ethR | 4326556 | c.-993A>G | upstream_gene_variant | 0.2 |
ethA | 4326563 | p.Ala304Gly | missense_variant | 0.19 |
ethR | 4326565 | c.-984C>A | upstream_gene_variant | 0.19 |
ethR | 4326591 | c.-958A>G | upstream_gene_variant | 0.17 |
ethR | 4326598 | c.-951T>C | upstream_gene_variant | 0.19 |
ethR | 4326610 | c.-939G>C | upstream_gene_variant | 0.17 |
ethR | 4326613 | c.-936G>A | upstream_gene_variant | 0.17 |
ethR | 4326628 | c.-921G>A | upstream_gene_variant | 0.18 |
ethR | 4326637 | c.-912T>G | upstream_gene_variant | 0.16 |
ethR | 4326640 | c.-909C>T | upstream_gene_variant | 0.17 |
ethR | 4327300 | c.-249G>A | upstream_gene_variant | 0.16 |
ethR | 4327318 | c.-231T>G | upstream_gene_variant | 0.23 |
ethR | 4327327 | c.-222A>G | upstream_gene_variant | 0.15 |
ethR | 4327330 | c.-219G>A | upstream_gene_variant | 0.19 |
ethR | 4327335 | c.-214A>G | upstream_gene_variant | 0.17 |
ethR | 4327336 | c.-213A>G | upstream_gene_variant | 0.14 |
ethR | 4327390 | c.-159C>G | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338711 | c.-190C>A | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |