Run ID: SRR6982415
Sample name:
Date: 04-04-2023 18:36:41
Number of reads: 373222
Percentage reads mapped: 99.19
Strain: lineage4.9.1
Drug-resistance: HR-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 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
gid | 4407851 | c.351dupG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5946 | p.Arg236His | missense_variant | 0.17 |
gyrB | 6939 | p.Pro567Gln | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
fgd1 | 491295 | c.513C>A | synonymous_variant | 0.38 |
fgd1 | 491492 | p.Pro237His | missense_variant | 0.3 |
mshA | 576166 | c.819C>A | synonymous_variant | 0.18 |
mshA | 576186 | p.Pro280His | missense_variant | 0.18 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.23 |
rpoB | 761254 | p.Pro483His | missense_variant | 0.17 |
rpoB | 762691 | p.Pro962Gln | missense_variant | 0.18 |
rpoB | 762828 | p.Arg1008Ser | missense_variant | 0.22 |
rpoB | 763046 | p.Gln1080His | missense_variant | 0.15 |
rpoC | 763274 | c.-96G>T | upstream_gene_variant | 0.17 |
rpoC | 763887 | p.Arg173Leu | missense_variant | 0.21 |
rpoC | 764918 | p.Val517Leu | missense_variant | 0.12 |
rpoC | 765564 | p.Ser732* | stop_gained | 0.18 |
rpoC | 766666 | c.3297C>A | synonymous_variant | 0.18 |
rpoC | 766800 | p.Ala1144Asp | missense_variant | 0.22 |
rpoC | 766867 | c.3498C>A | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775745 | p.Met912Ile | missense_variant | 0.25 |
mmpL5 | 775751 | c.2730C>T | synonymous_variant | 0.18 |
mmpL5 | 775823 | c.2658G>T | synonymous_variant | 0.17 |
mmpL5 | 776074 | p.Val803Ile | missense_variant | 0.2 |
mmpL5 | 776534 | p.Lys649Asn | missense_variant | 0.15 |
mmpL5 | 777161 | p.Gln440His | missense_variant | 0.22 |
mmpL5 | 777880 | p.Asp201Tyr | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781403 | c.-157G>T | upstream_gene_variant | 0.2 |
fbiC | 1303134 | c.204G>T | synonymous_variant | 0.22 |
fbiC | 1303848 | p.Phe306Leu | missense_variant | 0.18 |
fbiC | 1304658 | c.1728C>A | synonymous_variant | 0.16 |
fbiC | 1305387 | p.Met819Ile | missense_variant | 0.17 |
Rv1258c | 1406165 | c.1176G>T | synonymous_variant | 0.17 |
Rv1258c | 1406183 | c.1158C>A | synonymous_variant | 0.18 |
Rv1258c | 1406872 | p.Gly157Cys | missense_variant | 0.22 |
embR | 1416817 | p.Lys177Asn | missense_variant | 0.25 |
embR | 1416894 | p.Asp152Tyr | missense_variant | 0.25 |
embR | 1417477 | c.-130C>A | upstream_gene_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471764 | n.-82C>A | upstream_gene_variant | 0.25 |
rrs | 1473180 | n.1335G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473324 | n.1479G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475200 | n.1546delG | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475279 | n.1622G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476119 | n.2462G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476433 | n.2776C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476541 | n.2884C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476563 | n.2906G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476612 | n.2955G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476626 | n.2969G>T | non_coding_transcript_exon_variant | 0.4 |
inhA | 1674377 | p.Pro59Gln | missense_variant | 0.4 |
rpsA | 1834043 | p.Glu168* | stop_gained | 0.17 |
rpsA | 1834234 | c.693G>T | synonymous_variant | 0.25 |
rpsA | 1834623 | p.Ser361* | stop_gained | 0.2 |
rpsA | 1834905 | p.Pro455Gln | missense_variant | 0.18 |
tlyA | 1917861 | c.-79G>T | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102340 | c.703C>A | synonymous_variant | 0.2 |
ndh | 2102772 | p.His91Asn | missense_variant | 0.22 |
ndh | 2102848 | p.Glu65Asp | missense_variant | 0.29 |
ndh | 2102917 | c.126G>T | synonymous_variant | 0.2 |
katG | 2154026 | p.Leu696Met | missense_variant | 0.18 |
katG | 2154247 | p.Pro622His | missense_variant | 0.22 |
katG | 2154273 | p.Lys613Asn | missense_variant | 0.2 |
katG | 2154401 | p.Arg571Ser | missense_variant | 0.25 |
katG | 2154496 | p.Ser539Tyr | missense_variant | 0.25 |
katG | 2155134 | c.978G>T | synonymous_variant | 0.33 |
katG | 2155137 | c.975G>A | synonymous_variant | 0.33 |
katG | 2155194 | c.918C>A | synonymous_variant | 0.29 |
katG | 2155950 | c.162C>A | synonymous_variant | 0.2 |
katG | 2156299 | c.-188G>T | upstream_gene_variant | 0.17 |
PPE35 | 2170082 | c.531T>G | synonymous_variant | 0.29 |
PPE35 | 2170560 | p.Gly18Val | missense_variant | 0.25 |
Rv1979c | 2222232 | c.933G>T | synonymous_variant | 0.2 |
Rv1979c | 2222643 | c.522C>A | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 0.8 |
pncA | 2289360 | c.-119G>T | upstream_gene_variant | 0.33 |
pncA | 2289513 | c.-272G>T | upstream_gene_variant | 0.18 |
pncA | 2289529 | c.-288G>T | upstream_gene_variant | 0.2 |
eis | 2715089 | p.Leu82Ile | missense_variant | 0.2 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 1.0 |
folC | 2746173 | p.Gly476Trp | missense_variant | 0.15 |
folC | 2746948 | c.651G>T | synonymous_variant | 0.23 |
folC | 2747353 | c.246C>A | synonymous_variant | 0.18 |
folC | 2747723 | c.-125G>A | upstream_gene_variant | 0.22 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3065615 | p.Asp193Tyr | missense_variant | 0.25 |
Rv2752c | 3065840 | p.Glu118* | stop_gained | 0.25 |
Rv2752c | 3065983 | p.Arg70Leu | missense_variant | 0.29 |
thyA | 3074430 | c.42G>T | synonymous_variant | 0.4 |
thyA | 3074547 | c.-76G>T | upstream_gene_variant | 0.22 |
ald | 3086828 | c.9C>A | synonymous_variant | 0.18 |
ald | 3087246 | p.Gln143Lys | missense_variant | 0.2 |
ald | 3087305 | c.486G>T | synonymous_variant | 0.17 |
ald | 3087731 | c.912G>T | synonymous_variant | 0.22 |
ald | 3087746 | c.927G>T | synonymous_variant | 0.2 |
ald | 3087932 | c.1113C>A | synonymous_variant | 0.22 |
fbiD | 3339379 | p.Asp88Tyr | missense_variant | 0.4 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
Rv3083 | 3449367 | c.864G>T | synonymous_variant | 0.2 |
whiB7 | 3568793 | c.-114C>A | upstream_gene_variant | 0.25 |
Rv3236c | 3612625 | c.492C>A | synonymous_variant | 0.4 |
Rv3236c | 3613003 | p.Leu38Phe | missense_variant | 0.3 |
fbiB | 3642496 | p.Leu321Pro | missense_variant | 0.17 |
rpoA | 3877557 | c.951C>A | synonymous_variant | 0.17 |
rpoA | 3877601 | p.Gln303Lys | missense_variant | 0.2 |
rpoA | 3877666 | p.Ser281Tyr | missense_variant | 0.2 |
rpoA | 3878398 | p.Ser37* | stop_gained | 0.18 |
rpoA | 3878552 | c.-45C>A | upstream_gene_variant | 0.67 |
rpoA | 3878650 | c.-143C>A | upstream_gene_variant | 1.0 |
clpC1 | 4038401 | p.Leu768Phe | missense_variant | 0.18 |
clpC1 | 4038497 | c.2203_2207dupATCAG | frameshift_variant | 0.18 |
clpC1 | 4040088 | p.Arg206Leu | missense_variant | 0.2 |
embC | 4241167 | c.1305C>A | synonymous_variant | 0.18 |
embC | 4241186 | p.Gly442Cys | missense_variant | 0.17 |
embC | 4241319 | p.Pro486Gln | missense_variant | 0.18 |
embC | 4241424 | p.Arg521Leu | missense_variant | 0.25 |
embC | 4241503 | c.1641G>T | synonymous_variant | 0.18 |
embC | 4242543 | p.Arg894Leu | missense_variant | 0.15 |
embA | 4244077 | p.Arg282Leu | missense_variant | 0.25 |
embA | 4244393 | c.1161G>T | synonymous_variant | 0.22 |
embA | 4245452 | c.2220G>T | synonymous_variant | 0.29 |
embB | 4245743 | c.-771C>A | upstream_gene_variant | 0.23 |
embB | 4247261 | p.Gln250Lys | missense_variant | 0.2 |
embB | 4247299 | c.786G>T | synonymous_variant | 0.2 |
embB | 4247403 | p.Ser297* | stop_gained | 0.43 |
embB | 4247499 | p.Pro329His | missense_variant | 0.4 |
embB | 4248453 | p.Trp647Leu | missense_variant | 0.29 |
embB | 4248919 | c.2406C>A | synonymous_variant | 0.22 |
embB | 4248940 | c.2427C>A | synonymous_variant | 0.18 |
aftB | 4267145 | c.1692G>T | synonymous_variant | 0.22 |
aftB | 4267494 | p.Gly448Val | missense_variant | 0.33 |
aftB | 4267687 | p.Gly384Cys | missense_variant | 0.29 |
aftB | 4268898 | c.-62G>T | upstream_gene_variant | 0.25 |
ubiA | 4269891 | c.-58G>T | upstream_gene_variant | 0.15 |
ubiA | 4269918 | c.-85G>T | upstream_gene_variant | 0.2 |
ethA | 4327275 | p.Arg67Ser | missense_variant | 0.2 |
ethR | 4327982 | p.Trp145Leu | missense_variant | 0.2 |
whiB6 | 4338341 | p.Leu61Met | missense_variant | 0.18 |
whiB6 | 4338586 | c.-65C>A | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |