Run ID: SRR13861439
Sample name:
Date: 03-04-2023 09:31:46
Number of reads: 342830
Percentage reads mapped: 5.72
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.62 | rifampicin |
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.18 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.17 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.18 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.18 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.18 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.18 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.18 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.17 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.17 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.17 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.2 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.33 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.2 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.18 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.17 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.2 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.2 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.2 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.2 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.2 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.18 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.2 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.2 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.22 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.2 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.17 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.17 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.18 |
gyrA | 8636 | c.1335A>G | synonymous_variant | 0.18 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.17 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.2 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.2 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.22 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.22 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.2 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.18 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.18 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.21 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.21 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.25 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.31 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.27 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.2 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.2 |
gyrA | 8779 | p.Asp493Ala | missense_variant | 0.23 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.23 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.25 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.25 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.27 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.27 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.27 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.23 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.31 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.29 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.27 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.27 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.33 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.25 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.18 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.18 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.17 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.2 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.2 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.2 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.21 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.21 |
ccsA | 620730 | c.840C>T | synonymous_variant | 0.23 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.23 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.23 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.23 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.23 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.21 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.23 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.27 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.29 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.29 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.29 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.33 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.62 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.67 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.73 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.71 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.57 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.57 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.5 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.6 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.56 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.5 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.5 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.53 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.53 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.5 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.53 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.53 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.53 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.47 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.47 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.25 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.22 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.18 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.2 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.22 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.18 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.18 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.18 |
rpoC | 763919 | c.550C>T | synonymous_variant | 0.21 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.2 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.23 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.21 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.19 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.2 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.17 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.18 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.18 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.19 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.2 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.2 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.15 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.18 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.17 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.17 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.18 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.15 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.15 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.2 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.22 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.25 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.25 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.25 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.18 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.18 |
rpoC | 765985 | c.2616C>T | synonymous_variant | 0.2 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.22 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.18 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.18 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.17 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.17 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.17 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.15 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.17 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.18 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.18 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.17 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.25 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.27 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.23 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.23 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.21 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.27 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.21 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.18 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.2 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.19 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.14 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.14 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.23 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.18 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.18 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.18 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.2 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.18 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.2 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.2 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.22 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.25 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.22 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.22 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.2 |
fbiC | 1305276 | c.2346G>C | synonymous_variant | 0.15 |
fbiC | 1305279 | p.His783Gln | missense_variant | 0.15 |
fbiC | 1305282 | c.2352T>C | synonymous_variant | 0.15 |
fbiC | 1305297 | c.2367G>C | synonymous_variant | 0.15 |
fbiC | 1305300 | c.2370A>G | synonymous_variant | 0.15 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.15 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.14 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.15 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.15 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.18 |
fbiC | 1305393 | c.2463T>C | synonymous_variant | 0.17 |
fbiC | 1305405 | c.2475A>G | synonymous_variant | 0.15 |
fbiC | 1305411 | c.2481C>T | synonymous_variant | 0.15 |
fbiC | 1305420 | c.2490C>G | synonymous_variant | 0.17 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.29 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.14 |
inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.14 |
inhA | 1673589 | c.-613A>G | upstream_gene_variant | 0.15 |
fabG1 | 1673596 | p.Lys53Asp | missense_variant | 0.13 |
fabG1 | 1673633 | p.Ser65Asn | missense_variant | 0.13 |
inhA | 1673646 | c.-556T>C | upstream_gene_variant | 0.13 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.33 |
inhA | 1674379 | c.178C>T | synonymous_variant | 0.29 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.29 |
inhA | 1674387 | c.186A>G | synonymous_variant | 0.25 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.22 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.3 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.3 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.3 |
inhA | 1674498 | c.297G>A | synonymous_variant | 0.3 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.18 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.2 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.2 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.22 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.3 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.3 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.27 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.33 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.33 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.4 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.21 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.15 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.15 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.15 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.15 |
rpsA | 1833851 | p.Lys104Gln | missense_variant | 1.0 |
ndh | 2101915 | c.1128T>C | synonymous_variant | 0.17 |
ndh | 2101918 | p.Arg375Ser | missense_variant | 0.15 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.17 |
ndh | 2101939 | c.1104A>C | synonymous_variant | 0.17 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.18 |
ndh | 2101966 | c.1077T>G | synonymous_variant | 0.2 |
ndh | 2101972 | c.1071G>C | synonymous_variant | 0.2 |
ndh | 2101978 | p.Asn355Asp | missense_variant | 0.2 |
ndh | 2101988 | p.Ala352Gly | missense_variant | 0.18 |
ndh | 2102009 | p.Ser345Asn | missense_variant | 0.18 |
ndh | 2102020 | c.1023A>G | synonymous_variant | 0.18 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.17 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.22 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.22 |
katG | 2155740 | p.Gly124Gln | missense_variant | 0.22 |
katG | 2155747 | p.Ala122Gly | missense_variant | 0.25 |
katG | 2155782 | c.330C>G | synonymous_variant | 0.29 |
Rv1979c | 2223241 | c.-77C>G | upstream_gene_variant | 1.0 |
pncA | 2289811 | c.-570C>T | upstream_gene_variant | 1.0 |
pncA | 2289994 | c.-753A>C | upstream_gene_variant | 1.0 |
kasA | 2518301 | p.His63Asp | missense_variant | 1.0 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.15 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.15 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.15 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.15 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.14 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.14 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.15 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.15 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.15 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.17 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.18 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.18 |
pepQ | 2859859 | p.Ala187Glu | missense_variant | 1.0 |
Rv2752c | 3064886 | p.Ala436Pro | missense_variant | 1.0 |
Rv2752c | 3064928 | c.1264T>C | synonymous_variant | 0.2 |
Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 0.2 |
Rv2752c | 3064935 | c.1257A>G | synonymous_variant | 0.2 |
Rv2752c | 3064941 | p.Gln417Glu | missense_variant | 0.18 |
Rv2752c | 3064947 | c.1245A>G | synonymous_variant | 0.18 |
Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 0.18 |
Rv2752c | 3064962 | c.1230C>A | synonymous_variant | 0.18 |
Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 0.17 |
Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.17 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.17 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.15 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.14 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.14 |
Rv2752c | 3065028 | c.1164G>C | synonymous_variant | 0.14 |
Rv2752c | 3065031 | c.1161G>C | synonymous_variant | 0.14 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.21 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.17 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.17 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
thyX | 3067640 | c.306G>C | synonymous_variant | 0.17 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.17 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.18 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.18 |
thyX | 3067682 | c.264G>C | synonymous_variant | 0.2 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.18 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.17 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.15 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.15 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.15 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.15 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.21 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.21 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.13 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.12 |
thyX | 3067874 | c.72C>A | synonymous_variant | 0.18 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.15 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.15 |
Rv3083 | 3449104 | p.Pro201Ala | missense_variant | 1.0 |
Rv3236c | 3612337 | c.779delG | frameshift_variant | 1.0 |
fbiA | 3640902 | p.Gln120His | missense_variant | 0.25 |
fbiB | 3641723 | c.189T>C | synonymous_variant | 1.0 |
rpoA | 3877740 | c.768G>T | synonymous_variant | 0.85 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.2 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.2 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.2 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.2 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.14 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.17 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.18 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.22 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.22 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.22 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.25 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.25 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.25 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.23 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.31 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.31 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.31 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.31 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.25 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.27 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.27 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.17 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.17 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.2 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.15 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.17 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.2 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.2 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.17 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.17 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.18 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.22 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.2 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.17 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.18 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.17 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.18 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.17 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.18 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.17 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.17 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.17 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.17 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.15 |
clpC1 | 4040596 | c.109C>T | synonymous_variant | 0.14 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.14 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.14 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.14 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.13 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.13 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.13 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.13 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.13 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.14 |
embC | 4241005 | c.1143G>T | synonymous_variant | 0.87 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.13 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.17 |
embC | 4241081 | c.1220delT | frameshift_variant | 0.87 |
embC | 4242746 | p.Pro962Ser | missense_variant | 1.0 |
embA | 4243969 | p.Val246Ala | missense_variant | 1.0 |
embB | 4246250 | c.-264G>C | upstream_gene_variant | 0.2 |
embA | 4246264 | p.His1011Arg | missense_variant | 0.18 |
embB | 4246274 | c.-240G>C | upstream_gene_variant | 0.18 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.17 |
embA | 4246308 | c.3076_3077insAG | frameshift_variant | 0.22 |
embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.2 |
embA | 4246329 | p.Thr1033Leu | missense_variant | 0.2 |
embB | 4246355 | c.-159G>C | upstream_gene_variant | 0.17 |
embA | 4246359 | p.Ala1043Pro | missense_variant | 0.17 |
embB | 4246364 | c.-150G>C | upstream_gene_variant | 0.15 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.14 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.15 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 0.15 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.17 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.17 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.17 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.14 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.15 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.14 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.14 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.14 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.14 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.22 |
aftB | 4268446 | p.Ala131Ser | missense_variant | 0.15 |
aftB | 4268793 | p.Val15Gly | missense_variant | 0.17 |