Run ID: SRR8692899
Sample name:
Date: 13-08-2023 22:51:33
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: Other
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.94 | linezolid |
ethA | 4326715 | p.Cys253* | stop_gained | 0.25 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5743 | c.504G>T | synonymous_variant | 0.27 |
gyrB | 5857 | c.618C>A | synonymous_variant | 0.14 |
gyrA | 6478 | c.-824G>T | upstream_gene_variant | 0.5 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.2 |
gyrB | 7113 | p.Thr625Ile | missense_variant | 0.22 |
gyrA | 8155 | p.Thr285Asn | missense_variant | 0.12 |
gyrA | 8172 | p.Val291Ile | missense_variant | 0.12 |
gyrA | 8231 | c.930C>A | synonymous_variant | 0.18 |
gyrA | 8817 | p.Ser506Gly | missense_variant | 0.29 |
fgd1 | 491022 | c.240C>G | synonymous_variant | 0.13 |
fgd1 | 491031 | c.249C>G | synonymous_variant | 0.12 |
fgd1 | 491043 | c.261T>C | synonymous_variant | 0.13 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.13 |
fgd1 | 491064 | c.282A>C | synonymous_variant | 0.13 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.12 |
fgd1 | 491082 | c.300T>G | synonymous_variant | 0.12 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.12 |
fgd1 | 491091 | c.309T>G | synonymous_variant | 0.12 |
fgd1 | 491095 | p.Val105Ile | missense_variant | 0.13 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.13 |
fgd1 | 491115 | c.333G>C | synonymous_variant | 0.13 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.13 |
fgd1 | 491133 | c.351A>C | synonymous_variant | 0.13 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.14 |
mshA | 575265 | c.-83C>A | upstream_gene_variant | 0.14 |
mshA | 575286 | c.-62G>T | upstream_gene_variant | 0.14 |
mshA | 576170 | p.Gln275Lys | missense_variant | 0.17 |
ccsA | 619886 | c.-5G>T | upstream_gene_variant | 0.17 |
ccsA | 619924 | p.Arg12Gly | missense_variant | 0.17 |
ccsA | 620134 | p.Ala82Pro | missense_variant | 0.18 |
ccsA | 620550 | c.660C>A | synonymous_variant | 0.25 |
rpoB | 759721 | c.-86G>T | upstream_gene_variant | 0.2 |
rpoB | 759735 | c.-72G>T | upstream_gene_variant | 0.2 |
rpoB | 759770 | c.-37C>A | upstream_gene_variant | 0.18 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.17 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.18 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.15 |
rpoB | 760260 | p.Pro152Thr | missense_variant | 0.15 |
rpoB | 760333 | p.Ser176* | stop_gained | 0.15 |
rpoB | 760445 | c.639C>A | synonymous_variant | 0.4 |
rpoB | 760635 | p.Pro277Thr | missense_variant | 0.22 |
rpoB | 760796 | c.990A>G | synonymous_variant | 0.33 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.27 |
rpoB | 760808 | c.1002C>G | synonymous_variant | 0.27 |
rpoB | 760811 | c.1005C>G | synonymous_variant | 0.25 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.25 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.25 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.3 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.3 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.3 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.3 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.3 |
rpoB | 760877 | c.1071G>T | synonymous_variant | 0.27 |
rpoB | 760880 | c.1074G>C | synonymous_variant | 0.27 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.27 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.27 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.3 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.38 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.38 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.38 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.33 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.4 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.67 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.5 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.5 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.5 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.5 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.5 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.5 |
rpoB | 761370 | p.Ile522Val | missense_variant | 0.5 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.2 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.17 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.15 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.15 |
rpoB | 761862 | p.Ala686Thr | missense_variant | 0.14 |
rpoB | 761867 | c.2061C>A | synonymous_variant | 0.14 |
rpoB | 761868 | p.Asp688Gln | missense_variant | 0.14 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.14 |
rpoB | 761876 | c.2070C>G | synonymous_variant | 0.15 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.15 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.14 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.15 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.17 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.18 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.18 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 0.18 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 0.22 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.12 |
rpoB | 762144 | p.Glu780* | stop_gained | 0.17 |
rpoB | 762160 | p.Arg785Leu | missense_variant | 0.14 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.18 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.18 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.15 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.17 |
rpoB | 762332 | c.2526C>T | synonymous_variant | 0.18 |
rpoB | 762520 | p.Thr905Ile | missense_variant | 0.15 |
rpoB | 762633 | p.Ala943Ser | missense_variant | 0.22 |
rpoB | 762730 | p.Gln975Arg | missense_variant | 0.18 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.22 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.22 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.15 |
rpoC | 764737 | c.1368G>T | synonymous_variant | 0.22 |
rpoC | 765528 | p.Gly720Val | missense_variant | 0.18 |
rpoC | 765933 | p.Gly855Val | missense_variant | 0.12 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.13 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.14 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.15 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.15 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.17 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.2 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.2 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.2 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.2 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.17 |
rpoC | 766102 | c.2733C>A | synonymous_variant | 0.17 |
rpoC | 766318 | p.Met983Ile | missense_variant | 0.17 |
rpoC | 766722 | p.Pro1118Gln | missense_variant | 0.17 |
rpoC | 766737 | p.Arg1123Leu | missense_variant | 0.15 |
rpoC | 766745 | p.Gly1126Cys | missense_variant | 0.14 |
rpoC | 766889 | p.Glu1174* | stop_gained | 0.17 |
rpoC | 766928 | p.Glu1187* | stop_gained | 0.15 |
rpoC | 766965 | p.Glu1199Gly | missense_variant | 0.18 |
rpoC | 766983 | p.Pro1205Gln | missense_variant | 0.22 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.15 |
mmpL5 | 775990 | c.2491C>T | synonymous_variant | 0.15 |
mmpL5 | 778311 | p.Gly57Val | missense_variant | 0.14 |
mmpL5 | 778383 | p.Val33Ala | missense_variant | 0.12 |
mmpR5 | 778475 | c.-515G>T | upstream_gene_variant | 0.17 |
mmpL5 | 778950 | c.-470C>T | upstream_gene_variant | 0.22 |
mmpL5 | 779448 | c.-968G>T | upstream_gene_variant | 0.25 |
rpsL | 781404 | c.-156G>T | upstream_gene_variant | 0.17 |
rpsL | 781815 | c.256C>A | synonymous_variant | 0.2 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.18 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.18 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.25 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.22 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.25 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.22 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.22 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.25 |
rplC | 800717 | c.-92C>A | upstream_gene_variant | 0.15 |
rplC | 800725 | c.-84C>T | upstream_gene_variant | 0.14 |
rplC | 801196 | p.His130Asp | missense_variant | 0.15 |
rplC | 801353 | p.Val182Ala | missense_variant | 0.17 |
fbiC | 1303346 | p.Gly139Asp | missense_variant | 0.17 |
fbiC | 1303417 | p.Gly163Cys | missense_variant | 0.22 |
fbiC | 1304520 | c.1590A>G | synonymous_variant | 0.22 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.33 |
fbiC | 1304533 | c.1603T>C | synonymous_variant | 0.33 |
fbiC | 1304544 | p.Asp538Glu | missense_variant | 0.38 |
fbiC | 1304547 | c.1617C>G | synonymous_variant | 0.38 |
fbiC | 1304556 | p.Asp542Glu | missense_variant | 0.33 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.38 |
fbiC | 1304562 | c.1632G>C | synonymous_variant | 0.38 |
fbiC | 1304567 | p.Phe546Tyr | missense_variant | 0.38 |
fbiC | 1304571 | c.1641G>C | synonymous_variant | 0.44 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.3 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.25 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.18 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.17 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.15 |
fbiC | 1304663 | p.Ser578Leu | missense_variant | 0.14 |
fbiC | 1304850 | c.1920C>T | synonymous_variant | 0.33 |
fbiC | 1305051 | c.2121G>C | synonymous_variant | 0.25 |
Rv1258c | 1406273 | c.1068C>T | synonymous_variant | 0.15 |
Rv1258c | 1406626 | p.Tyr239His | missense_variant | 0.25 |
Rv1258c | 1406647 | p.Asp232Tyr | missense_variant | 0.33 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.5 |
Rv1258c | 1407378 | c.-38C>A | upstream_gene_variant | 0.29 |
embR | 1416416 | p.Gly311Val | missense_variant | 0.2 |
embR | 1417029 | p.Asp107Tyr | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473942 | n.285G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474408 | n.751G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474437 | n.780G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474449 | n.792G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475417 | n.1760G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475454 | n.1797G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.18 |
inhA | 1674759 | c.558G>T | synonymous_variant | 0.18 |
rpsA | 1833425 | c.-117C>A | upstream_gene_variant | 0.25 |
rpsA | 1833691 | p.Glu50Asp | missense_variant | 0.15 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.22 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.2 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.2 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.18 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.25 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.22 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.2 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.2 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.2 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.2 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.31 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.38 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.31 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.29 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.27 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.36 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.36 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.4 |
rpsA | 1834487 | p.Gly316Cys | missense_variant | 0.13 |
rpsA | 1834623 | p.Ser361* | stop_gained | 0.2 |
rpsA | 1834901 | p.Ala454Pro | missense_variant | 0.33 |
katG | 2154417 | c.1695G>T | synonymous_variant | 0.18 |
katG | 2154464 | p.Ala550Ser | missense_variant | 0.2 |
katG | 2154480 | c.1632C>A | synonymous_variant | 0.18 |
katG | 2155434 | c.678G>A | synonymous_variant | 0.15 |
katG | 2156162 | c.-51G>T | upstream_gene_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.12 |
PPE35 | 2168240 | c.2373C>A | synonymous_variant | 0.2 |
PPE35 | 2168280 | p.Pro778Gln | missense_variant | 0.17 |
PPE35 | 2168540 | c.2073C>T | synonymous_variant | 0.33 |
PPE35 | 2168593 | p.Pro674Thr | missense_variant | 0.67 |
PPE35 | 2170504 | p.Glu37* | stop_gained | 0.18 |
Rv1979c | 2223267 | c.-103T>C | upstream_gene_variant | 0.2 |
Rv1979c | 2223323 | c.-159T>C | upstream_gene_variant | 0.17 |
pncA | 2289221 | c.21C>A | synonymous_variant | 0.17 |
pncA | 2289431 | c.-190G>A | upstream_gene_variant | 0.29 |
pncA | 2289752 | c.-511G>A | upstream_gene_variant | 0.15 |
eis | 2714309 | p.Pro342Thr | missense_variant | 0.15 |
folC | 2746173 | p.Gly476Trp | missense_variant | 0.29 |
folC | 2746227 | p.Gly458Trp | missense_variant | 0.25 |
folC | 2746272 | p.Ala443Ser | missense_variant | 0.25 |
pepQ | 2859819 | c.600G>T | synonymous_variant | 0.13 |
ribD | 2987154 | c.316C>A | synonymous_variant | 0.25 |
ribD | 2987347 | p.Pro170Gln | missense_variant | 0.18 |
Rv2752c | 3065262 | p.Glu310Asp | missense_variant | 0.12 |
Rv2752c | 3065406 | c.786C>A | synonymous_variant | 0.2 |
Rv2752c | 3065409 | p.Phe261Leu | missense_variant | 0.22 |
Rv2752c | 3065473 | p.Ser240Tyr | missense_variant | 0.17 |
Rv2752c | 3065557 | p.Gly212Val | missense_variant | 0.2 |
Rv2752c | 3065995 | p.His66Arg | missense_variant | 0.12 |
Rv2752c | 3066275 | c.-84G>A | upstream_gene_variant | 0.25 |
Rv2752c | 3066329 | c.-138C>A | upstream_gene_variant | 0.18 |
thyA | 3073832 | p.Glu214* | stop_gained | 0.18 |
thyA | 3073851 | p.His207Gln | missense_variant | 0.25 |
thyA | 3074086 | p.Ile129Ser | missense_variant | 0.12 |
ald | 3086825 | c.6C>A | synonymous_variant | 0.29 |
ald | 3087243 | p.Ala142Ser | missense_variant | 0.23 |
ald | 3087299 | p.Met160Ile | missense_variant | 0.18 |
fbiD | 3339195 | c.78G>T | synonymous_variant | 0.17 |
fbiD | 3339373 | p.Glu86* | stop_gained | 0.14 |
fbiD | 3339472 | p.Ala119Pro | missense_variant | 0.13 |
Rv3083 | 3448437 | c.-67C>A | upstream_gene_variant | 0.15 |
Rv3083 | 3449034 | c.531C>A | synonymous_variant | 0.18 |
Rv3083 | 3449515 | p.Glu338Gln | missense_variant | 0.2 |
Rv3083 | 3449825 | p.Ser441Tyr | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.26 |
fprA | 3474276 | c.270C>A | synonymous_variant | 0.13 |
Rv3236c | 3612156 | p.Arg321Cys | missense_variant | 0.17 |
Rv3236c | 3612901 | c.216C>A | synonymous_variant | 0.15 |
Rv3236c | 3613204 | c.-88G>T | upstream_gene_variant | 0.17 |
fbiB | 3640839 | c.-696C>A | upstream_gene_variant | 0.15 |
fbiA | 3640876 | p.His112Asn | missense_variant | 0.17 |
fbiA | 3641140 | p.Ile200Leu | missense_variant | 0.29 |
alr | 3840692 | c.729C>A | synonymous_variant | 0.15 |
alr | 3840915 | p.Pro169Gln | missense_variant | 0.2 |
alr | 3841444 | c.-24G>T | upstream_gene_variant | 0.2 |
rpoA | 3877553 | p.Glu319* | stop_gained | 0.17 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.14 |
rpoA | 3877888 | p.Ala207Glu | missense_variant | 0.22 |
rpoA | 3877940 | p.Asp190Tyr | missense_variant | 0.15 |
ddn | 3986818 | c.-26G>T | upstream_gene_variant | 0.29 |
ddn | 3987112 | p.Leu90Pro | missense_variant | 0.17 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.17 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.17 |
clpC1 | 4038533 | p.Arg724Gln | missense_variant | 0.18 |
clpC1 | 4038536 | c.2169C>G | synonymous_variant | 0.17 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.17 |
clpC1 | 4038587 | c.2118C>T | synonymous_variant | 0.27 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.23 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.23 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.23 |
clpC1 | 4038614 | c.2091C>T | synonymous_variant | 0.23 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 0.21 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.21 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.2 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.2 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.2 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.33 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.25 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.22 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.25 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.17 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.17 |
clpC1 | 4038881 | c.1824C>G | synonymous_variant | 0.18 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.2 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.22 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.22 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.22 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.22 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.36 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.36 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.23 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.17 |
clpC1 | 4039262 | c.1443C>T | synonymous_variant | 0.22 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.22 |
clpC1 | 4039277 | c.1428C>A | synonymous_variant | 0.25 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.22 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.2 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.22 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.22 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.22 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.25 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.22 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.25 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.29 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.33 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.33 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.33 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.33 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.33 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.29 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.33 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.2 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.2 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.2 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.2 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.22 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.2 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.23 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.23 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.25 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.25 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.23 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.23 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.27 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.27 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.22 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.15 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.15 |
clpC1 | 4040093 | c.612C>T | synonymous_variant | 0.15 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.2 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.2 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.2 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.2 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.2 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.18 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.15 |
clpC1 | 4040219 | c.486C>T | synonymous_variant | 0.25 |
clpC1 | 4040453 | c.252C>A | synonymous_variant | 0.15 |
clpC1 | 4040830 | c.-126G>A | upstream_gene_variant | 0.15 |
panD | 4043873 | p.Gly137Cys | missense_variant | 0.2 |
panD | 4043898 | c.384G>T | synonymous_variant | 0.15 |
panD | 4044044 | p.His80Asn | missense_variant | 0.17 |
panD | 4044087 | c.195C>A | synonymous_variant | 0.17 |
panD | 4044111 | c.171C>A | synonymous_variant | 0.18 |
embC | 4240228 | c.366G>T | synonymous_variant | 0.13 |
embC | 4240654 | c.792C>A | synonymous_variant | 0.22 |
embC | 4240672 | c.810C>A | synonymous_variant | 0.2 |
embC | 4241143 | c.1281C>A | synonymous_variant | 0.17 |
embC | 4241160 | p.Ala433Asp | missense_variant | 0.17 |
embC | 4241282 | p.Ala474Thr | missense_variant | 0.14 |
embA | 4243260 | p.His10Asn | missense_variant | 0.14 |
embA | 4243328 | c.96G>A | synonymous_variant | 0.17 |
embA | 4243337 | c.105G>A | synonymous_variant | 0.18 |
embA | 4243679 | c.447C>A | synonymous_variant | 0.15 |
embA | 4243826 | c.594G>A | synonymous_variant | 0.2 |
embA | 4243957 | p.Pro242Gln | missense_variant | 0.17 |
embA | 4243970 | c.738C>A | synonymous_variant | 0.18 |
embA | 4245018 | p.Gly596Cys | missense_variant | 0.2 |
embA | 4245053 | c.1821G>T | synonymous_variant | 0.17 |
embA | 4245206 | c.1974A>G | synonymous_variant | 0.18 |
embA | 4245208 | p.Leu659Trp | missense_variant | 0.18 |
embA | 4245778 | p.Ala849Asp | missense_variant | 0.17 |
embB | 4245791 | c.-723C>T | upstream_gene_variant | 0.17 |
embB | 4246448 | c.-66C>A | upstream_gene_variant | 0.14 |
embB | 4246578 | p.Ser22Tyr | missense_variant | 0.4 |
embB | 4247089 | c.576G>C | synonymous_variant | 0.12 |
embB | 4247191 | c.678C>A | synonymous_variant | 0.17 |
aftB | 4266995 | c.1842G>C | synonymous_variant | 0.22 |
aftB | 4267743 | p.Arg365Gln | missense_variant | 0.17 |
aftB | 4267785 | p.Gly351Val | missense_variant | 0.18 |
aftB | 4267961 | c.876C>A | synonymous_variant | 0.2 |
aftB | 4267966 | p.Arg291Ser | missense_variant | 0.2 |
aftB | 4268150 | p.Met229Ile | missense_variant | 0.2 |
aftB | 4269678 | c.-842C>A | upstream_gene_variant | 0.22 |
ubiA | 4269689 | p.Val49Ile | missense_variant | 0.2 |
ubiA | 4269730 | p.Ala35Glu | missense_variant | 0.22 |
ethA | 4326208 | c.1266G>T | synonymous_variant | 0.15 |
ethA | 4326247 | p.Met409Ile | missense_variant | 0.13 |
ethA | 4326376 | c.1098G>T | synonymous_variant | 0.18 |
ethA | 4326448 | c.1026G>T | synonymous_variant | 0.15 |
ethR | 4327102 | c.-447G>T | upstream_gene_variant | 0.17 |
ethR | 4327636 | p.Leu30Ile | missense_variant | 0.25 |
whiB6 | 4338538 | c.-17T>C | upstream_gene_variant | 0.33 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.14 |