Run ID: SRR22528522
Sample name:
Date: 04-04-2023 04:17:48
Number of reads: 2079870
Percentage reads mapped: 99.63
Strain: lineage4.1.1
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Cys | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6052 | p.Ile271Met | missense_variant | 1.0 |
gyrB | 7221 | p.Ser661Thr | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416699 | p.Leu217Val | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673865 | c.-337C>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 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087828 | p.Pro337Thr | missense_variant | 0.19 |
fbiD | 3339744 | c.627A>C | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568405 | p.Ala92Gly | missense_variant | 0.12 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.15 |
whiB7 | 3568441 | p.Lys80Thr | missense_variant | 0.13 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.19 |
clpC1 | 4040902 | c.-198T>G | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.99 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.2 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.15 |
embB | 4247039 | p.Phe176Val | missense_variant | 0.17 |
embB | 4247051 | p.Asn180His | missense_variant | 0.15 |
embB | 4247055 | p.Leu181Gln | missense_variant | 0.26 |
embB | 4247080 | p.Phe189Leu | missense_variant | 0.16 |
embB | 4248319 | c.1806A>T | synonymous_variant | 0.2 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.14 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408099 | p.Leu35Arg | missense_variant | 1.0 |