Run ID: SRR13861549
Sample name:
Date: 03-04-2023 09:34:37
Number of reads: 233694
Percentage reads mapped: 5.85
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 | 0.2 | rifampicin |
rrs | 1472122 | n.277G>C | non_coding_transcript_exon_variant | 0.83 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5319 | p.Arg27Leu | missense_variant | 1.0 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.18 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.29 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.38 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.33 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.33 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.38 |
gyrA | 7649 | c.348C>T | synonymous_variant | 0.22 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.22 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.2 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.2 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.18 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.18 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.18 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.18 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.18 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.17 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.18 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.2 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.2 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.18 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.2 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.2 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.2 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.2 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.2 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.2 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.2 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.2 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.18 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.18 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.2 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.22 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.22 |
rpoB | 760867 | p.Gly354Asp | missense_variant | 1.0 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.2 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.2 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.25 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.38 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.25 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.25 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.22 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.38 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.38 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.25 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.33 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.33 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.33 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.25 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.25 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.29 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.25 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.22 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.22 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.15 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.17 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.2 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.2 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.25 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.17 |
rpoB | 761815 | p.Ala670Glu | missense_variant | 0.17 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.23 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.23 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.23 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.25 |
rpoB | 761864 | c.2058G>C | synonymous_variant | 0.25 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.23 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.21 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.21 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.21 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.15 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.15 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.15 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.18 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.18 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.18 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.2 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.2 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.27 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.43 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.29 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.21 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.2 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.21 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.23 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.25 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.22 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.27 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.18 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.15 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.17 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.23 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.23 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.23 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.23 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.2 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.19 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.13 |
rpoB | 762496 | c.2691delC | frameshift_variant | 0.93 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.33 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.29 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.29 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.44 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.3 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.3 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.3 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.33 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.3 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.27 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.27 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.3 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.3 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.31 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.44 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.44 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.44 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.44 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.47 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.47 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.5 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.5 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.54 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.54 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.54 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.54 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.54 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.54 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.54 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.54 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.54 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.54 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.5 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.5 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.46 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.3 |
rpoC | 766563 | p.Thr1065Ser | missense_variant | 1.0 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.18 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.18 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.18 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.2 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.2 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.17 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.18 |
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 | 0.25 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.18 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.19 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.21 |
mmpL5 | 775976 | c.2505G>C | synonymous_variant | 1.0 |
mmpL5 | 776814 | p.Gln556Arg | missense_variant | 1.0 |
rplC | 800623 | c.-186A>C | upstream_gene_variant | 0.91 |
rplC | 800769 | c.-40A>T | upstream_gene_variant | 0.67 |
fbiC | 1302878 | c.-53C>G | upstream_gene_variant | 1.0 |
fbiC | 1303535 | p.Ser202Leu | missense_variant | 1.0 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.25 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.25 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.25 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.25 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.29 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.33 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.29 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.33 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.4 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.4 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.4 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.67 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.5 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.5 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.4 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.4 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.33 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.25 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.25 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.25 |
atpE | 1461189 | c.145C>T | synonymous_variant | 0.25 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.25 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.25 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.25 |
atpE | 1461224 | c.180T>C | synonymous_variant | 0.25 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.29 |
atpE | 1461256 | p.Met71Arg | missense_variant | 0.8 |
rrs | 1471836 | n.-10A>G | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474409 | n.756_766delACCCACACGCG | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474427 | n.770A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474434 | n.777T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.42 |
inhA | 1674231 | c.30T>C | synonymous_variant | 0.22 |
inhA | 1674237 | c.36T>C | synonymous_variant | 0.2 |
inhA | 1674239 | p.Ser13Thr | missense_variant | 0.2 |
inhA | 1674243 | c.42A>G | synonymous_variant | 0.2 |
inhA | 1674279 | c.78A>C | synonymous_variant | 0.14 |
inhA | 1674281 | p.Arg27Gln | missense_variant | 0.14 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.18 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.18 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.17 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.2 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.2 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.25 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.29 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.29 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.29 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.4 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.4 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.4 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.43 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.29 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.22 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.22 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.27 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.25 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.27 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.33 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.25 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.29 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.31 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.25 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.31 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.33 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.33 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.33 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.36 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.42 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.38 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.33 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.36 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.27 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.33 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.22 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.22 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.18 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.2 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.18 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.15 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.14 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.14 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.15 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.33 |
katG | 2155740 | p.Gly124Gln | missense_variant | 0.33 |
katG | 2155747 | p.Ala122Gly | missense_variant | 0.33 |
katG | 2156157 | c.-46C>A | upstream_gene_variant | 1.0 |
PPE35 | 2168627 | p.Ile662Met | missense_variant | 1.0 |
Rv1979c | 2222100 | c.1065T>A | synonymous_variant | 1.0 |
pncA | 2289242 | c.-1T>C | upstream_gene_variant | 1.0 |
kasA | 2518138 | c.24T>C | synonymous_variant | 0.33 |
kasA | 2518146 | p.Phe11Tyr | missense_variant | 0.29 |
kasA | 2518162 | c.48G>A | synonymous_variant | 0.29 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.29 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.29 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.25 |
kasA | 2518222 | c.108G>A | synonymous_variant | 0.22 |
kasA | 2518223 | c.109_111delTTGinsCTC | synonymous_variant | 0.22 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.2 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.22 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.17 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.17 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.2 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.2 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.2 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.25 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.25 |
kasA | 2518843 | c.729T>C | synonymous_variant | 0.29 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.18 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.27 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.25 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.25 |
folC | 2747394 | p.Ile69Val | missense_variant | 0.18 |
folC | 2747395 | c.204T>C | synonymous_variant | 0.17 |
folC | 2747407 | c.192T>C | synonymous_variant | 0.17 |
folC | 2747411 | p.Ser63Ala | missense_variant | 0.2 |
folC | 2747416 | c.183A>G | synonymous_variant | 0.2 |
folC | 2747419 | c.180C>G | synonymous_variant | 0.2 |
folC | 2747430 | c.169C>T | synonymous_variant | 0.2 |
folC | 2747439 | p.Met54Leu | missense_variant | 0.18 |
folC | 2747442 | c.157T>C | synonymous_variant | 0.18 |
folC | 2747443 | c.156G>A | synonymous_variant | 0.18 |
folC | 2747464 | c.135G>C | synonymous_variant | 0.2 |
ribD | 2987205 | p.Ser123Ala | missense_variant | 1.0 |
ribD | 2987347 | p.Pro170Leu | missense_variant | 1.0 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.5 |
Rv3083 | 3448903 | p.Asp134His | missense_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.29 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.29 |
fprA | 3473836 | c.-171C>A | upstream_gene_variant | 0.33 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.29 |
Rv3236c | 3612621 | c.496T>C | synonymous_variant | 0.18 |
Rv3236c | 3612628 | c.489G>C | synonymous_variant | 0.18 |
Rv3236c | 3612643 | c.474A>G | synonymous_variant | 0.18 |
Rv3236c | 3612667 | c.450T>G | synonymous_variant | 0.18 |
Rv3236c | 3612673 | c.444G>C | synonymous_variant | 0.17 |
Rv3236c | 3612676 | c.441A>G | synonymous_variant | 0.17 |
Rv3236c | 3612685 | c.432C>T | synonymous_variant | 0.17 |
Rv3236c | 3612694 | p.Arg141His | missense_variant | 0.17 |
Rv3236c | 3612708 | c.409T>C | synonymous_variant | 0.18 |
Rv3236c | 3612715 | c.402G>C | synonymous_variant | 0.15 |
Rv3236c | 3612721 | c.396G>C | synonymous_variant | 0.18 |
Rv3236c | 3612724 | c.393T>C | synonymous_variant | 0.18 |
Rv3236c | 3612730 | c.387C>G | synonymous_variant | 0.15 |
Rv3236c | 3612748 | c.369G>C | synonymous_variant | 0.15 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.18 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.18 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.2 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.18 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.2 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.22 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.29 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.25 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.25 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.22 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.25 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.29 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.25 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.29 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.25 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.38 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.33 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.33 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.33 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.4 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.4 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.4 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.4 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.18 |
clpC1 | 4039663 | p.Gly348Ser | missense_variant | 1.0 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.29 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.29 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.33 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.33 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.33 |
embC | 4240204 | c.342T>C | synonymous_variant | 0.2 |
embC | 4240210 | c.348C>G | synonymous_variant | 0.2 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.2 |
embC | 4240258 | c.396T>G | synonymous_variant | 0.25 |
embC | 4240267 | c.405T>C | synonymous_variant | 0.25 |
embC | 4240270 | c.408T>C | synonymous_variant | 0.25 |
embC | 4240277 | p.Leu139Val | missense_variant | 0.29 |
embC | 4240282 | c.420C>G | synonymous_variant | 0.29 |
embC | 4240285 | c.423C>G | synonymous_variant | 0.29 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.22 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.22 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.3 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.2 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.18 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.2 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.17 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.17 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.17 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.17 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.15 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.18 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.22 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.2 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.2 |
embC | 4240954 | p.Ile364Met | missense_variant | 0.2 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.2 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.22 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.22 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.22 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.25 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.29 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.29 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.29 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.29 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.33 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.33 |
embC | 4241256 | p.Arg465Thr | missense_variant | 1.0 |
embB | 4245617 | c.-897C>G | upstream_gene_variant | 0.2 |
embB | 4245620 | c.-894T>C | upstream_gene_variant | 0.2 |
embB | 4245623 | c.-891G>C | upstream_gene_variant | 0.2 |
embB | 4245626 | c.-888G>C | upstream_gene_variant | 0.2 |
embA | 4245643 | p.Ala804Val | missense_variant | 0.25 |
embA | 4245648 | p.Ile806Tyr | missense_variant | 0.25 |
embA | 4245652 | p.Thr807Ser | missense_variant | 0.25 |
embB | 4245659 | c.-855C>G | upstream_gene_variant | 0.25 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 0.25 |
embB | 4245677 | c.-837G>C | upstream_gene_variant | 0.25 |
embB | 4245680 | c.-834G>A | upstream_gene_variant | 0.22 |
embB | 4245683 | c.-831C>G | upstream_gene_variant | 0.2 |
embB | 4245689 | c.-825C>G | upstream_gene_variant | 0.22 |
embB | 4245692 | c.-822G>C | upstream_gene_variant | 0.22 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.22 |
embB | 4245701 | c.-813G>C | upstream_gene_variant | 0.2 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.29 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.25 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.25 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.29 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.43 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.33 |
embA | 4246449 | p.Val1073Phe | missense_variant | 1.0 |
aftB | 4268192 | c.645G>C | synonymous_variant | 1.0 |