Run ID: ERR176518
Sample name:
Date: 31-03-2023 15:03:50
Number of reads: 2051335
Percentage reads mapped: 76.04
Strain: lineage4.3.4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.96 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.95 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.14 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.14 |
gyrA | 7415 | c.114C>A | synonymous_variant | 0.15 |
gyrA | 7418 | c.117C>T | synonymous_variant | 0.14 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.18 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.18 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.16 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.16 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.14 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.14 |
gyrA | 7763 | c.462T>G | synonymous_variant | 0.15 |
gyrA | 7781 | c.480G>T | synonymous_variant | 0.13 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.15 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.14 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.14 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.13 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.13 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.13 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.13 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.12 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.13 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.15 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.23 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.22 |
gyrA | 8261 | c.960C>A | synonymous_variant | 0.2 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.19 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.21 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.2 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.23 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.24 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.26 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.24 |
gyrA | 8339 | c.1038A>C | synonymous_variant | 0.15 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.14 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.12 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.12 |
gyrA | 8852 | c.1551T>G | synonymous_variant | 0.15 |
gyrA | 8858 | c.1557T>G | synonymous_variant | 0.16 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.15 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.16 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.17 |
gyrA | 8900 | c.1599G>C | synonymous_variant | 0.17 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.17 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.16 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.13 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.13 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.18 |
gyrA | 9329 | c.2028C>G | synonymous_variant | 0.14 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.13 |
gyrA | 9341 | c.2040C>G | synonymous_variant | 0.12 |
ccsA | 620649 | c.759A>G | synonymous_variant | 0.14 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.2 |
ccsA | 620691 | c.801G>C | synonymous_variant | 0.19 |
ccsA | 620694 | c.804C>G | synonymous_variant | 0.16 |
ccsA | 620698 | p.Val270Ile | missense_variant | 0.18 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.17 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.2 |
ccsA | 620724 | c.834C>T | synonymous_variant | 0.2 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.21 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.19 |
ccsA | 620748 | c.858T>C | synonymous_variant | 0.21 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.16 |
ccsA | 620783 | p.Ala298Val | missense_variant | 0.14 |
ccsA | 620787 | c.897C>A | synonymous_variant | 0.14 |
ccsA | 620793 | c.903G>C | synonymous_variant | 0.14 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.14 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.17 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.21 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.31 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.31 |
rpoB | 760271 | c.465C>G | synonymous_variant | 0.29 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.23 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.18 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.14 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.15 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.17 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.18 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.18 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.21 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.22 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.23 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.22 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.2 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.2 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.18 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.18 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.15 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.15 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.15 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.14 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.14 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.15 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.15 |
rpoB | 760566 | p.Ser254Ala | missense_variant | 0.15 |
rpoB | 760567 | c.762delG | frameshift_variant | 0.15 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.13 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.15 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.18 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.21 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.22 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.22 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.21 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.22 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.22 |
rpoB | 760703 | c.897C>T | synonymous_variant | 0.14 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.14 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.14 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.13 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.12 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.15 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.17 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.16 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.13 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.14 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.16 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.15 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.15 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.17 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.14 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.14 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.12 |
rpoB | 761892 | p.Ile696Val | missense_variant | 0.12 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 0.14 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.21 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.24 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.24 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.3 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.26 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.18 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.17 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.16 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.19 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.13 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.13 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762179 | c.2373C>A | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.16 |
rpoB | 762209 | c.2403C>T | synonymous_variant | 0.21 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.17 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.19 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.19 |
rpoB | 762275 | c.2469C>G | synonymous_variant | 0.14 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.14 |
rpoB | 762299 | c.2493G>C | synonymous_variant | 0.14 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.13 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.13 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.14 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.13 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.13 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.21 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.2 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.21 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.18 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.18 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.23 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.18 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.17 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.17 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.23 |
rpoC | 763100 | c.-270G>A | upstream_gene_variant | 0.21 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.21 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.16 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.16 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.12 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.11 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.21 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.17 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.17 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.18 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.2 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.19 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.18 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.13 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.18 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.16 |
rpoC | 764084 | p.Asn239Val | missense_variant | 0.16 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.18 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.11 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.15 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.21 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.16 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.14 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.15 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.15 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.14 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.13 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.14 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.13 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.15 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.16 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.14 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.18 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.2 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.24 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.28 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.29 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.3 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.36 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.38 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.36 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.3 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.26 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.23 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.2 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764908 | c.1539G>A | synonymous_variant | 0.12 |
rpoC | 764926 | c.1557C>T | synonymous_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.94 |
rpoC | 765425 | p.Lys686Glu | missense_variant | 0.13 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.15 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.15 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.15 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.15 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.17 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.18 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.14 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.17 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.22 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.22 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.21 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.21 |
rpoC | 765958 | c.2589C>G | synonymous_variant | 0.21 |
rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 0.19 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.19 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.2 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.19 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.18 |
rpoC | 766518 | p.Thr1050Ser | missense_variant | 0.19 |
rpoC | 766525 | c.3156G>C | synonymous_variant | 0.18 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.16 |
rpoC | 766530 | p.Arg1054Gln | missense_variant | 0.16 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.22 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.23 |
rpoC | 766546 | p.Glu1059Asp | missense_variant | 0.22 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.22 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.17 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.15 |
rpoC | 766582 | c.3213C>T | synonymous_variant | 0.16 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.16 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.15 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.14 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.14 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.12 |
rpoC | 766807 | c.3438T>C | synonymous_variant | 0.13 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 0.12 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.17 |
mmpL5 | 775946 | c.2535C>G | synonymous_variant | 0.23 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.24 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.23 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.21 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.24 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.19 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.19 |
mmpL5 | 776000 | c.2481G>C | synonymous_variant | 0.15 |
mmpL5 | 776003 | p.Ile826Leu | missense_variant | 0.15 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.19 |
mmpL5 | 776030 | c.2451G>C | synonymous_variant | 0.2 |
mmpL5 | 776042 | c.2439C>G | synonymous_variant | 0.16 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.12 |
mmpL5 | 777133 | p.Val450Ile | missense_variant | 0.14 |
mmpL5 | 777142 | p.Val447Leu | missense_variant | 0.16 |
mmpL5 | 777170 | c.1311T>C | synonymous_variant | 0.16 |
mmpL5 | 777173 | c.1308C>G | synonymous_variant | 0.16 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.16 |
mmpL5 | 777179 | c.1302G>C | synonymous_variant | 0.17 |
mmpL5 | 777182 | c.1299C>G | synonymous_variant | 0.18 |
mmpL5 | 777188 | c.1293T>C | synonymous_variant | 0.21 |
mmpL5 | 777194 | c.1287A>G | synonymous_variant | 0.2 |
mmpL5 | 777209 | c.1272C>T | synonymous_variant | 0.18 |
mmpL5 | 777215 | c.1266C>T | synonymous_variant | 0.17 |
mmpL5 | 777225 | p.Asn419Ser | missense_variant | 0.17 |
mmpL5 | 777245 | c.1236G>C | synonymous_variant | 0.16 |
mmpL5 | 777251 | c.1230C>G | synonymous_variant | 0.14 |
mmpL5 | 777254 | c.1227G>C | synonymous_variant | 0.14 |
mmpL5 | 777278 | c.1203G>C | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.12 |
rpsL | 781718 | c.159C>T | synonymous_variant | 0.12 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.15 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.13 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.12 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.15 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.15 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.22 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.21 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.2 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.21 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.23 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.24 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.24 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.25 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.24 |
rpsL | 781889 | c.330C>T | synonymous_variant | 0.25 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.24 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.19 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.19 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.13 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.13 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.13 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.14 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.14 |
fbiC | 1303525 | p.Ser199Ala | missense_variant | 0.16 |
fbiC | 1303531 | p.Met201Leu | missense_variant | 0.15 |
fbiC | 1303542 | c.612C>G | synonymous_variant | 0.16 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.16 |
fbiC | 1303554 | c.624G>A | synonymous_variant | 0.2 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.23 |
fbiC | 1303581 | c.651G>C | synonymous_variant | 0.2 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.2 |
fbiC | 1303590 | c.660A>T | synonymous_variant | 0.18 |
fbiC | 1303598 | p.Phe223Tyr | missense_variant | 0.16 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.15 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.15 |
fbiC | 1304613 | c.1683T>G | synonymous_variant | 0.12 |
fbiC | 1304637 | c.1707G>A | synonymous_variant | 0.12 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.14 |
fbiC | 1304664 | c.1734G>C | synonymous_variant | 0.14 |
fbiC | 1304682 | c.1752C>G | synonymous_variant | 0.12 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.12 |
fbiC | 1305318 | c.2388C>G | synonymous_variant | 0.13 |
fbiC | 1305330 | c.2400C>G | synonymous_variant | 0.15 |
fbiC | 1305331 | p.Glu801Gln | missense_variant | 0.15 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.15 |
fbiC | 1305339 | c.2409C>T | synonymous_variant | 0.15 |
fbiC | 1305351 | c.2421G>C | synonymous_variant | 0.15 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.17 |
fbiC | 1305393 | c.2463T>A | synonymous_variant | 0.13 |
fbiC | 1305400 | p.His824Asn | missense_variant | 0.12 |
fbiC | 1305405 | c.2475A>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473823 | n.166T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473831 | n.174G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475353 | n.1696A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475354 | n.1697A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475366 | n.1709G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475398 | n.1741C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475403 | n.1746T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475404 | n.1747A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475429 | n.1772G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475989 | n.2332T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476692 | n.3035T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.12 |
rpsA | 1833772 | c.231C>T | synonymous_variant | 0.22 |
rpsA | 1833778 | c.237C>T | synonymous_variant | 0.22 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.22 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.2 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.22 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.24 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.23 |
rpsA | 1833817 | c.276C>T | synonymous_variant | 0.24 |
rpsA | 1833820 | c.279G>A | synonymous_variant | 0.24 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.22 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.23 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.22 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.17 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.22 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.19 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.19 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.21 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.19 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.18 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.17 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.17 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.14 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.15 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.13 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.12 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.12 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.13 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.18 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.21 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.18 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.17 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.17 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.2 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.13 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.17 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.15 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.14 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.14 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.14 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.14 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 0.14 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.13 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.15 |
rpsA | 1834699 | p.Glu386Asp | missense_variant | 0.16 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.16 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.23 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.18 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.16 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.23 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.14 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.14 |
thyA | 3073998 | c.474G>A | synonymous_variant | 0.15 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.27 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.13 |
rpoA | 3877644 | c.864C>T | synonymous_variant | 0.16 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.16 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.17 |
rpoA | 3877671 | c.837C>G | synonymous_variant | 0.16 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.17 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 0.19 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.19 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.22 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.22 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.2 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.16 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.16 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.17 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 0.17 |
rpoA | 3877794 | c.714G>C | synonymous_variant | 0.14 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.17 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.17 |
rpoA | 3877842 | c.666A>G | synonymous_variant | 0.13 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.14 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.13 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.17 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.19 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.2 |
rpoA | 3877884 | c.624G>C | synonymous_variant | 0.2 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.22 |
rpoA | 3877905 | c.603A>C | synonymous_variant | 0.24 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.22 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.18 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.19 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.14 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.15 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.18 |
rpoA | 3878626 | c.-119A>C | upstream_gene_variant | 0.24 |
ddn | 3986661 | c.-183C>A | upstream_gene_variant | 0.2 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.17 |
ddn | 3986681 | c.-163C>G | upstream_gene_variant | 0.16 |
ddn | 3986687 | c.-157C>T | upstream_gene_variant | 0.14 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038569 | c.2136C>T | synonymous_variant | 0.14 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.14 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.19 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.22 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.24 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.25 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.24 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGT | synonymous_variant | 0.24 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.17 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.29 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.19 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.12 |
clpC1 | 4038932 | c.1773G>A | synonymous_variant | 0.18 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.16 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.16 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.19 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.21 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.21 |
clpC1 | 4038995 | c.1708_1710delTTGinsCTC | synonymous_variant | 0.22 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.24 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.23 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.19 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.16 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.17 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.17 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.14 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.14 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.11 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.16 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.18 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.2 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.14 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.14 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.13 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.13 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.14 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039526 | c.1179G>A | synonymous_variant | 0.19 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.17 |
clpC1 | 4039559 | c.1146C>T | synonymous_variant | 0.19 |
clpC1 | 4039566 | p.Val380Ala | missense_variant | 0.19 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.19 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.2 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.2 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.19 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.19 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.16 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.12 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.12 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.13 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.13 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.15 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.17 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.25 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.23 |
clpC1 | 4039997 | c.708C>A | synonymous_variant | 0.24 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.26 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.26 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.24 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.25 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.25 |
embC | 4242422 | p.Trp854Gly | missense_variant | 0.26 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.32 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243566 | p.Asp112His | missense_variant | 0.98 |
aftB | 4267601 | c.1236C>G | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |