Run ID: SRR22528537
Sample name:
Date: 04-04-2023 04:18:18
Number of reads: 3800765
Percentage reads mapped: 99.63
Strain: lineage4.3.3
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 760628 | p.Lys274Asn | missense_variant | 0.48 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.22 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303701 | c.771C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519104 | c.990T>G | synonymous_variant | 0.12 |
pepQ | 2860113 | c.306C>G | synonymous_variant | 0.14 |
pepQ | 2860140 | c.279A>G | synonymous_variant | 0.13 |
pepQ | 2860144 | p.Val92Gly | missense_variant | 0.24 |
pepQ | 2860153 | p.Glu89Ala | missense_variant | 0.16 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568411 | p.Ala90Gly | missense_variant | 0.13 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.12 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.21 |
Rv3236c | 3612853 | c.264C>T | synonymous_variant | 1.0 |
rpoA | 3878653 | c.-146A>C | upstream_gene_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.15 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.16 |
embB | 4247039 | p.Phe176Val | missense_variant | 0.11 |
embB | 4247055 | p.Leu181Gln | missense_variant | 0.17 |
embB | 4248319 | c.1806A>C | synonymous_variant | 0.15 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |