Run ID: ERR11465511
Sample name:
Date: 09-01-2024 23:53:23
Number of reads: 1362538
Percentage reads mapped: 80.98
Strain: lineage4.3.4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
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 | 0.92 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5611 | c.372C>T | synonymous_variant | 1.0 |
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.2 |
gyrA | 6724 | c.-578G>C | upstream_gene_variant | 0.15 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.19 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.17 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.15 |
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 0.15 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.2 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 0.22 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.27 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.28 |
gyrA | 6838 | c.-464C>A | upstream_gene_variant | 0.25 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.24 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.25 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.2 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.15 |
gyrA | 7355 | c.54T>C | synonymous_variant | 0.16 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7406 | c.105G>T | synonymous_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.23 |
gyrA | 7763 | c.462T>A | synonymous_variant | 0.23 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.29 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.24 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.23 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.23 |
gyrA | 7802 | c.501C>G | synonymous_variant | 0.23 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.2 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.25 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.28 |
gyrA | 7841 | c.540C>G | synonymous_variant | 0.33 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.15 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.17 |
gyrA | 8930 | c.1629C>T | synonymous_variant | 0.16 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.26 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.27 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.23 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.22 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.22 |
gyrA | 9038 | c.1737C>G | synonymous_variant | 0.24 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.21 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.21 |
gyrA | 9062 | c.1761C>G | synonymous_variant | 0.2 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.23 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.3 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.3 |
gyrA | 9092 | c.1791C>G | synonymous_variant | 0.3 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 0.26 |
gyrA | 9114 | p.Glu605Asn | missense_variant | 0.24 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.21 |
gyrA | 9128 | c.1827C>G | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9332 | p.Asn677Lys | missense_variant | 0.35 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.32 |
gyrA | 9341 | c.2040C>G | synonymous_variant | 0.26 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.27 |
gyrA | 9353 | c.2052G>C | synonymous_variant | 0.25 |
gyrA | 9356 | c.2055G>C | synonymous_variant | 0.25 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.23 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.21 |
mshA | 575842 | c.495G>C | synonymous_variant | 0.17 |
mshA | 575845 | c.498C>G | synonymous_variant | 0.19 |
ccsA | 620694 | c.804C>G | synonymous_variant | 0.24 |
ccsA | 620712 | c.822G>C | synonymous_variant | 0.21 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.22 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.23 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.26 |
ccsA | 620736 | c.846G>C | synonymous_variant | 0.26 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.24 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.24 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.24 |
ccsA | 620769 | c.879C>G | synonymous_variant | 0.25 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.24 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.24 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.2 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.19 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.21 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.26 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.33 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.21 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.21 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.21 |
rpoB | 760551 | c.745_746delTCinsAG | synonymous_variant | 0.21 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.22 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.31 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.2 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.18 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.19 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.21 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.18 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.21 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.2 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.24 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.24 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.31 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.31 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.24 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.2 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.19 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.15 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.22 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.24 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.35 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.39 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.35 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.38 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.29 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.29 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.15 |
rpoC | 763160 | c.-210G>T | upstream_gene_variant | 0.25 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.24 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.19 |
rpoC | 763501 | c.132C>T | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.24 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.24 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.32 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.15 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.15 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.16 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.19 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.17 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.26 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.24 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.14 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.15 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.17 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.16 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.16 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.16 |
rpoC | 764857 | c.1488G>T | synonymous_variant | 0.2 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.2 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.27 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.95 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.27 |
rpoC | 765480 | p.Tyr704Phe | missense_variant | 0.27 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.28 |
rpoC | 765499 | c.2130C>A | synonymous_variant | 0.3 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.29 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.13 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 0.21 |
rpoC | 766009 | c.2640G>T | synonymous_variant | 0.25 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 0.23 |
rpoC | 766459 | c.3090G>C | synonymous_variant | 0.23 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.21 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.19 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.19 |
rpoC | 766492 | c.3123T>G | synonymous_variant | 0.2 |
rpoC | 766493 | p.Gly1042Asn | missense_variant | 0.2 |
rpoC | 766517 | p.Thr1050Ser | missense_variant | 0.22 |
rpoC | 766525 | c.3156G>T | synonymous_variant | 0.2 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.21 |
rpoC | 766530 | p.Arg1054Gln | missense_variant | 0.2 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.23 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.23 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.19 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.21 |
rpoC | 766573 | c.3204T>G | synonymous_variant | 0.22 |
rpoC | 766582 | c.3213C>T | synonymous_variant | 0.24 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.24 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.26 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.25 |
rpoC | 766624 | c.3255G>C | synonymous_variant | 0.24 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.24 |
rpoC | 766634 | p.Phe1089Ile | missense_variant | 0.25 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.16 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.2 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.26 |
rpoC | 766694 | p.Gln1109Asp | missense_variant | 0.26 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.26 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.24 |
rpoC | 766711 | c.3342C>T | synonymous_variant | 0.24 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.19 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.26 |
rpoC | 766732 | c.3363G>T | synonymous_variant | 0.27 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.28 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.29 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.31 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.32 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.3 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.35 |
rpoC | 766776 | p.Arg1136His | missense_variant | 0.35 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.28 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766807 | c.3438T>C | synonymous_variant | 0.22 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 0.28 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775915 | p.Ala856Ser | missense_variant | 0.2 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.26 |
mmpL5 | 775922 | c.2559G>C | synonymous_variant | 0.27 |
mmpL5 | 775943 | c.2538C>G | synonymous_variant | 0.14 |
mmpL5 | 775946 | c.2535C>G | synonymous_variant | 0.31 |
mmpL5 | 775951 | c.2530C>T | synonymous_variant | 0.45 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.36 |
mmpL5 | 775975 | p.Leu836Met | missense_variant | 0.38 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.3 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.25 |
mmpL5 | 775997 | c.2484T>G | synonymous_variant | 0.24 |
mmpL5 | 776000 | p.Leu827Ile | missense_variant | 0.24 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.28 |
mmpL5 | 776021 | c.2460G>A | synonymous_variant | 0.4 |
mmpL5 | 776024 | c.2457G>C | synonymous_variant | 0.41 |
mmpL5 | 776030 | c.2451G>C | synonymous_variant | 0.43 |
mmpL5 | 776060 | c.2421C>G | synonymous_variant | 0.28 |
mmpL5 | 776072 | c.2409C>G | synonymous_variant | 0.21 |
mmpL5 | 776075 | c.2406C>G | synonymous_variant | 0.21 |
mmpL5 | 776080 | p.Ala801Ser | missense_variant | 0.27 |
mmpL5 | 776645 | c.1836C>G | synonymous_variant | 0.18 |
mmpL5 | 776650 | p.Asp611Asn | missense_variant | 0.2 |
mmpL5 | 776654 | c.1827A>C | synonymous_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.18 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.21 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.22 |
rpsL | 781676 | c.117C>G | synonymous_variant | 0.24 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.24 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.25 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.24 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.24 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.26 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.31 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.33 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.35 |
rpsL | 781754 | c.195G>A | synonymous_variant | 0.36 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.36 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.32 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.17 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.15 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.2 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.2 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.2 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.27 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.26 |
rpsL | 781895 | c.336G>A | synonymous_variant | 0.25 |
rpsL | 781898 | c.339A>G | synonymous_variant | 0.24 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.24 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.28 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.28 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.16 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.2 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.19 |
rplC | 800672 | c.-137G>T | upstream_gene_variant | 0.21 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.21 |
rplC | 800693 | c.-116A>T | upstream_gene_variant | 0.21 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.23 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.24 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.22 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.17 |
fbiC | 1303531 | p.Met201Leu | missense_variant | 0.21 |
fbiC | 1303548 | c.618G>C | synonymous_variant | 0.17 |
fbiC | 1303551 | c.621G>T | synonymous_variant | 0.18 |
fbiC | 1304613 | c.1683T>G | synonymous_variant | 0.16 |
atpE | 1461050 | c.6C>T | synonymous_variant | 0.17 |
atpE | 1461056 | c.12T>A | synonymous_variant | 0.16 |
atpE | 1461089 | c.45G>C | synonymous_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472445 | n.601_604delTCTC | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472451 | n.606_607insCGGG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472463 | n.618G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474287 | n.630_635delTCCTTTinsCTCGACTTG | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474294 | n.638_649delCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474708 | n.1052_1053insACAAG | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474711 | n.1055_1058delGTGT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474720 | n.1063C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475989 | n.2332T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.32 |
inhA | 1674864 | c.663C>T | synonymous_variant | 0.37 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.35 |
inhA | 1674876 | c.675C>G | synonymous_variant | 0.33 |
inhA | 1674879 | c.678T>G | synonymous_variant | 0.32 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.21 |
rpsA | 1833745 | c.204G>T | synonymous_variant | 0.15 |
rpsA | 1833772 | c.231C>T | synonymous_variant | 0.3 |
rpsA | 1833778 | c.237C>T | synonymous_variant | 0.28 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.25 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.17 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.17 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.23 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.21 |
rpsA | 1833820 | c.279G>A | synonymous_variant | 0.24 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.2 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.19 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.2 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.24 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.22 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.25 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.25 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.28 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.23 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.2 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.19 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.22 |
rpsA | 1834282 | c.741C>T | synonymous_variant | 0.16 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.15 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.23 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.27 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.27 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.28 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.27 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.29 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.31 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.16 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.33 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.32 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.34 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.42 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.42 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.4 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.19 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.19 |
rpsA | 1834678 | c.1137C>T | synonymous_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518651 | c.537C>G | synonymous_variant | 0.24 |
kasA | 2518656 | p.Ala181Gly | missense_variant | 0.24 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.29 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.3 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.25 |
kasA | 2519137 | c.1023T>G | synonymous_variant | 0.5 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.37 |
kasA | 2519152 | c.1038G>C | synonymous_variant | 0.37 |
kasA | 2519158 | c.1044C>G | synonymous_variant | 0.32 |
Rv2752c | 3065249 | c.943T>C | synonymous_variant | 0.31 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.21 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.21 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.91 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
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 | 3877656 | c.852T>G | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.21 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.24 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.25 |
rpoA | 3877842 | c.666A>G | synonymous_variant | 0.23 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.25 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.27 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.29 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.25 |
rpoA | 3877884 | c.624G>C | synonymous_variant | 0.25 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.26 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.24 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.23 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.22 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.19 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.22 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.15 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.17 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.2 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.17 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.19 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.24 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.24 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.2 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.2 |
rpoA | 3878175 | c.333G>C | synonymous_variant | 0.19 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.16 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.18 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.18 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.21 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.21 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.25 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.14 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.15 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.14 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.16 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.17 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.17 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.17 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.17 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.16 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.16 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.19 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.17 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.15 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.19 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.19 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.15 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.23 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.21 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.21 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.19 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.18 |
clpC1 | 4040693 | c.12A>T | synonymous_variant | 0.29 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.26 |
embC | 4241047 | c.1185C>T | synonymous_variant | 0.25 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.16 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |