Run ID: SRR3675252
Sample name:
Date: 04-04-2023 05:24:18
Number of reads: 497722
Percentage reads mapped: 92.23
Strain: lineage1.1.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761090 | p.Ser428Arg | missense_variant | 0.17 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.26 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.16 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 6529 | c.-773G>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7894 | p.Ala198Val | missense_variant | 0.15 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8657 | c.1356C>T | synonymous_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765649 | p.Phe760Leu | missense_variant | 0.2 |
rpoC | 766691 | p.Gly1108Cys | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776045 | c.2436G>T | synonymous_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406294 | c.1047C>A | synonymous_variant | 0.17 |
Rv1258c | 1406503 | p.Val280Leu | missense_variant | 1.0 |
embR | 1416443 | p.Pro302Gln | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1461087 | p.Leu15Met | missense_variant | 0.15 |
atpE | 1461090 | p.Ile16Val | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472790 | n.945T>C | 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 | 0.19 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
inhA | 1674325 | p.Asp42Asn | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154673 | p.Ala480Val | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154887 | p.Ala409Ser | missense_variant | 0.33 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168991 | p.Ala541Val | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.43 |
Rv1979c | 2222089 | p.Leu359Ser | missense_variant | 0.15 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290135 | c.-894C>A | upstream_gene_variant | 0.33 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2714803 | p.Ala177Glu | missense_variant | 0.17 |
eis | 2715235 | p.Ala33Glu | missense_variant | 0.13 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.4 |
folC | 2746896 | p.Gly235Trp | missense_variant | 0.22 |
folC | 2747639 | c.-41C>A | upstream_gene_variant | 0.17 |
ribD | 2987168 | c.330C>A | synonymous_variant | 0.13 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyX | 3068138 | c.-193C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338919 | c.-199C>A | upstream_gene_variant | 0.12 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.33 |
fbiD | 3339712 | p.Arg199Cys | missense_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612401 | p.Ser239Leu | missense_variant | 0.13 |
Rv3236c | 3612879 | p.Thr80Ala | missense_variant | 0.17 |
rpoA | 3878200 | p.Gly103Asp | missense_variant | 0.17 |
rpoA | 3878238 | p.Asp90Glu | missense_variant | 0.29 |
clpC1 | 4038679 | p.Pro676Thr | missense_variant | 0.12 |
clpC1 | 4038899 | c.1806C>A | synonymous_variant | 0.2 |
clpC1 | 4040306 | c.399G>A | synonymous_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239835 | c.-28C>A | upstream_gene_variant | 0.29 |
embC | 4240318 | c.456T>C | synonymous_variant | 0.15 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243115 | p.Leu1085Met | missense_variant | 0.2 |
embC | 4243119 | p.Trp1086* | stop_gained | 0.18 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244073 | p.Ala281Ser | missense_variant | 0.13 |
embA | 4244555 | p.Gln441His | missense_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.83 |
aftB | 4268156 | c.681C>T | synonymous_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4270023 | c.-190G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338224 | c.297delC | frameshift_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338598 | c.-77G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407713 | p.Gly164Cys | missense_variant | 0.17 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |