Run ID: SRR6257080
Sample name:
Date: 04-04-2023 13:25:33
Number of reads: 726644
Percentage reads mapped: 100.0
Strain: lineage4.8
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
pncA | 2288953 | p.Gly97Ser | missense_variant | 1.0 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 1.0 | kanamycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6208 | c.969G>T | synonymous_variant | 0.17 |
gyrB | 7025 | p.Lys596Glu | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9140 | p.Gln613His | missense_variant | 0.12 |
rpoB | 759915 | p.Lys37Glu | missense_variant | 0.11 |
rpoC | 767309 | p.Asp1314Tyr | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801227 | p.Gly140Val | missense_variant | 0.14 |
Rv1258c | 1407094 | p.Gly83Cys | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472818 | n.973C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473934 | n.277G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475226 | n.1569C>A | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673155 | c.-285G>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154619 | p.Arg498Leu | missense_variant | 0.15 |
katG | 2154654 | p.Ser486Arg | missense_variant | 0.13 |
katG | 2155430 | p.Ile228Leu | missense_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169830 | p.Asn261Lys | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518693 | c.579C>A | synonymous_variant | 0.15 |
eis | 2714397 | p.His312Gln | missense_variant | 0.11 |
folC | 2746724 | p.Pro292Leu | missense_variant | 0.11 |
Rv2752c | 3067004 | c.-813C>A | upstream_gene_variant | 0.12 |
thyX | 3067913 | c.33G>T | synonymous_variant | 0.12 |
thyX | 3067921 | p.Val9Leu | missense_variant | 0.12 |
thyA | 3074422 | p.Pro17Leu | missense_variant | 1.0 |
thyA | 3074598 | c.-127A>G | upstream_gene_variant | 0.15 |
ald | 3087248 | p.Gln143His | missense_variant | 0.13 |
ald | 3087302 | c.483C>A | synonymous_variant | 0.12 |
fbiD | 3339701 | p.Leu195Pro | missense_variant | 0.12 |
fbiB | 3642748 | p.Ala405Asp | missense_variant | 0.17 |
clpC1 | 4038197 | c.2508A>G | synonymous_variant | 0.13 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.12 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243770 | p.Gly180* | stop_gained | 0.12 |
embA | 4243793 | c.561C>A | synonymous_variant | 0.12 |
embA | 4245994 | p.Ala921Glu | missense_variant | 0.12 |
embB | 4247693 | p.Ala394Ser | missense_variant | 0.14 |
embB | 4248036 | p.Val508Gly | missense_variant | 1.0 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.19 |
aftB | 4268805 | p.Thr11Lys | missense_variant | 0.12 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.11 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408102 | p.Gly34Glu | missense_variant | 1.0 |