Run ID: SRR18715189
Sample name:
Date: 03-04-2023 20:23:06
Number of reads: 2645920
Percentage reads mapped: 99.78
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 |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
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 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.22 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.65 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.25 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.44 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.43 |
rpoB | 762423 | p.Ile873Phe | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.34 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.15 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.21 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.31 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.33 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.5 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.43 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.5 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.67 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.92 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.26 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.2 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.17 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.24 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408010 | p.Val65Phe | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |