Run ID: SRR19303775
Sample name:
Date: 03-04-2023 21:06:12
Number of reads: 1103329
Percentage reads mapped: 41.56
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.12 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7650 | p.Gly117Ser | missense_variant | 0.12 |
gyrA | 8649 | p.Arg450Gly | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9367 | p.Ala689Gly | missense_variant | 1.0 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.21 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.21 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.26 |
rpoC | 764537 | p.Pro390Val | missense_variant | 0.28 |
rpoC | 764540 | p.Val391Ile | missense_variant | 0.32 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.3 |
rpoC | 764549 | p.Pro394Ala | missense_variant | 0.3 |
rpoC | 764552 | p.Gly395Asn | missense_variant | 0.32 |
rpoC | 764557 | p.Asn396Lys | missense_variant | 0.3 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.29 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.29 |
rpoC | 764576 | p.Ser403Ala | missense_variant | 0.29 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.28 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.31 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.41 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.37 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.33 |
rpoC | 764621 | c.1252_1254delCTCinsTTG | synonymous_variant | 0.33 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.33 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.3 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.19 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.19 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.19 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.19 |
rpoC | 764689 | c.1320G>A | synonymous_variant | 0.19 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.19 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.19 |
rpoC | 764705 | p.Leu446Lys | missense_variant | 0.19 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.17 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777484 | p.Gln333Glu | missense_variant | 0.97 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918064 | p.Pro42Arg | missense_variant | 0.21 |
tlyA | 1918066 | p.Ala43Pro | missense_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.98 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.75 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.23 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
ddn | 3986682 | c.-162A>G | upstream_gene_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.2 |
embC | 4240422 | p.Glu187Val | missense_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.29 |
embB | 4248319 | c.1806A>C | synonymous_variant | 0.25 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.5 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |