Run ID: ERR6336801
Sample name:
Date: 02-04-2023 02:03:54
Number of reads: 573965
Percentage reads mapped: 99.02
Strain: lineage1.2.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
tlyA | 1918473 | c.536delC | frameshift_variant | 0.2 | capreomycin |
thyA | 3074095 | p.Arg126Gln | missense_variant | 0.22 | para-aminosalicylic_acid |
gid | 4407796 | p.Ser136* | stop_gained | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5963 | p.Ala242Thr | missense_variant | 0.2 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7369 | p.Glu23Gly | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8303 | p.His334Gln | missense_variant | 0.15 |
gyrA | 8442 | p.Leu381Val | missense_variant | 0.2 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Ile | missense_variant | 0.15 |
fgd1 | 491511 | p.Leu243Phe | missense_variant | 0.17 |
fgd1 | 491513 | p.Asn244Ser | missense_variant | 0.18 |
fgd1 | 491516 | p.Asn245Ser | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575175 | c.-173G>A | upstream_gene_variant | 0.14 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575714 | p.Tyr123His | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.43 |
mshA | 576289 | c.942G>A | synonymous_variant | 0.15 |
mshA | 576721 | p.Glu458Asp | missense_variant | 0.2 |
mshA | 576738 | p.Val464Gly | missense_variant | 0.22 |
ccsA | 620616 | c.726C>T | synonymous_variant | 0.15 |
rpoB | 759775 | c.-32G>A | upstream_gene_variant | 0.13 |
rpoB | 760717 | p.Arg304His | missense_variant | 0.12 |
rpoB | 761749 | p.Ser648Leu | missense_variant | 0.18 |
rpoB | 762945 | p.Thr1047Ala | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763247 | c.-123G>A | upstream_gene_variant | 0.12 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763659 | p.Leu97Pro | missense_variant | 0.11 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765055 | c.1686C>T | synonymous_variant | 0.14 |
rpoC | 766089 | p.Asp907Ala | missense_variant | 0.29 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777403 | p.Val360Met | missense_variant | 0.22 |
mmpS5 | 778736 | p.Glu57Gly | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781667 | c.108C>T | synonymous_variant | 0.12 |
rpsL | 781750 | p.Thr64Met | missense_variant | 0.17 |
rplC | 801303 | c.495G>A | synonymous_variant | 0.13 |
rplC | 801410 | p.Arg201His | missense_variant | 0.17 |
rplC | 801441 | c.633G>A | synonymous_variant | 0.15 |
fbiC | 1304358 | c.1428C>T | synonymous_variant | 0.13 |
Rv1258c | 1406308 | p.Arg345Gly | missense_variant | 0.13 |
Rv1258c | 1406674 | p.Arg223Trp | missense_variant | 0.17 |
Rv1258c | 1407394 | c.-54C>T | upstream_gene_variant | 0.13 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417082 | p.Asp89Gly | missense_variant | 0.18 |
embR | 1417169 | c.177_178delCT | frameshift_variant | 0.12 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
atpE | 1461078 | p.Gly12Ser | missense_variant | 0.12 |
atpE | 1461130 | p.Gly29Asp | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472753 | n.908A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472759 | n.914T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473219 | n.1374T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474060 | n.403G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474732 | n.1075A>G | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673986 | p.Pro183Ser | missense_variant | 0.18 |
inhA | 1674484 | p.Ile95Leu | missense_variant | 1.0 |
rpsA | 1833840 | p.Leu100Pro | missense_variant | 0.12 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
tlyA | 1917823 | c.-117C>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102398 | c.645C>T | synonymous_variant | 0.22 |
katG | 2154037 | p.Ser692Thr | missense_variant | 0.43 |
katG | 2154043 | p.Thr690Asn | missense_variant | 0.25 |
katG | 2154174 | c.1938C>T | synonymous_variant | 0.17 |
katG | 2154255 | c.1857C>T | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168417 | c.2196C>T | synonymous_variant | 0.18 |
Rv1979c | 2222249 | p.Val306Ile | missense_variant | 0.13 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222640 | c.525G>A | synonymous_variant | 0.15 |
Rv1979c | 2222737 | p.Gly143Asp | missense_variant | 0.15 |
Rv1979c | 2222839 | p.Leu109Ser | missense_variant | 0.15 |
Rv1979c | 2223105 | c.60C>T | synonymous_variant | 0.13 |
Rv1979c | 2223204 | c.-40T>C | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289234 | p.Ala3Val | missense_variant | 0.12 |
pncA | 2289237 | p.Arg2Gln | missense_variant | 0.12 |
pncA | 2289884 | c.-644_-643insA | upstream_gene_variant | 0.22 |
pncA | 2290073 | c.-832T>C | upstream_gene_variant | 0.18 |
pncA | 2290196 | c.-955A>G | upstream_gene_variant | 0.11 |
kasA | 2517954 | c.-161G>A | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518397 | c.286delG | frameshift_variant | 0.12 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519188 | c.1074G>A | synonymous_variant | 0.18 |
eis | 2714858 | p.Gly159Ser | missense_variant | 0.33 |
ahpC | 2725962 | c.-231C>T | upstream_gene_variant | 0.18 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746530 | p.Ala357Thr | missense_variant | 0.29 |
folC | 2747462 | p.Ser46Asn | missense_variant | 0.14 |
pepQ | 2859568 | p.Ala284Val | missense_variant | 0.15 |
pepQ | 2859768 | p.Phe217Leu | missense_variant | 0.14 |
ribD | 2987206 | p.Ser123Cys | missense_variant | 0.13 |
ribD | 2987571 | p.Thr245Ser | missense_variant | 0.18 |
Rv2752c | 3064552 | p.Arg547His | missense_variant | 0.18 |
Rv2752c | 3065212 | p.Thr327Met | missense_variant | 0.2 |
Rv2752c | 3066286 | c.-95C>T | upstream_gene_variant | 0.13 |
thyA | 3074162 | p.Pro104Ser | missense_variant | 0.33 |
thyA | 3074245 | p.Gly76Glu | missense_variant | 0.17 |
thyA | 3074407 | p.Thr22Ile | missense_variant | 0.12 |
thyA | 3074497 | c.-26G>A | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087350 | c.531C>G | synonymous_variant | 0.13 |
ald | 3087414 | p.Ile199Phe | missense_variant | 0.13 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.23 |
fbiD | 3339744 | c.627A>C | synonymous_variant | 0.22 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448748 | p.Arg82Gln | missense_variant | 0.14 |
Rv3083 | 3448996 | p.His165Tyr | missense_variant | 0.14 |
Rv3083 | 3449025 | p.Asp174Glu | missense_variant | 0.12 |
Rv3083 | 3449295 | c.792G>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474700 | p.Gly232Ser | missense_variant | 0.12 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475192 | p.Lys396Glu | missense_variant | 0.13 |
fprA | 3475344 | p.Ser446Arg | missense_variant | 0.25 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612568 | c.549G>A | synonymous_variant | 0.25 |
Rv3236c | 3612776 | p.Asp114Val | missense_variant | 0.13 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3641104 | p.Val188Phe | missense_variant | 1.0 |
fbiB | 3642501 | p.Ser323Arg | missense_variant | 0.21 |
alr | 3840829 | p.Val198Ile | missense_variant | 0.17 |
alr | 3841222 | p.Ala67Thr | missense_variant | 0.12 |
rpoA | 3877837 | p.Glu224Ala | missense_variant | 0.11 |
rpoA | 3878483 | c.25C>T | synonymous_variant | 0.12 |
rpoA | 3878501 | p.Ile3Phe | missense_variant | 0.14 |
clpC1 | 4040338 | p.Val123Met | missense_variant | 0.17 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240411 | c.549G>C | synonymous_variant | 0.22 |
embC | 4240553 | p.Met231Leu | missense_variant | 0.12 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240841 | p.Tyr327His | missense_variant | 0.11 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241046 | p.Gly395Val | missense_variant | 0.29 |
embC | 4241822 | p.Phe654Ile | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243751 | c.519C>T | synonymous_variant | 0.15 |
embA | 4244132 | c.900G>A | synonymous_variant | 0.15 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244491 | p.Thr420Met | missense_variant | 0.4 |
embA | 4245218 | c.1986C>T | synonymous_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.22 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.29 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.33 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.33 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.33 |
embB | 4247322 | p.Pro270Leu | missense_variant | 0.25 |
embB | 4247424 | p.Leu304Pro | missense_variant | 0.12 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248319 | c.1806A>T | synonymous_variant | 0.33 |
embB | 4248753 | p.Cys747Tyr | missense_variant | 0.15 |
embB | 4249354 | c.2841G>A | synonymous_variant | 0.13 |
aftB | 4268296 | p.Cys181Arg | missense_variant | 0.13 |
aftB | 4268367 | p.Cys157Tyr | missense_variant | 0.13 |
aftB | 4269231 | c.-395C>T | upstream_gene_variant | 0.17 |
aftB | 4269267 | c.-431C>T | upstream_gene_variant | 0.18 |
ubiA | 4269325 | c.508delA | frameshift_variant | 0.15 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269505 | p.Gly110Glu | missense_variant | 0.14 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338325 | p.Ala66Gly | missense_variant | 0.12 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338443 | p.Tyr27His | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | 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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408174 | p.Ala10Gly | missense_variant | 0.11 |