Run ID: SRR11033643
Sample name:
Date: 02-04-2023 20:04:56
Number of reads: 1683159
Percentage reads mapped: 99.71
Strain: lineage4.3.3
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7994 | c.693C>A | synonymous_variant | 0.14 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8959 | p.Asp553Gly | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576133 | c.786A>C | synonymous_variant | 0.18 |
rpoB | 760540 | p.Arg245Gln | missense_variant | 0.12 |
rpoB | 762026 | c.2220G>T | synonymous_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779074 | p.Ser29Pro | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 1.0 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472414 | n.569C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473227 | n.1382C>A | non_coding_transcript_exon_variant | 0.33 |
inhA | 1674299 | p.Gly33Val | missense_variant | 0.11 |
rpsA | 1834036 | c.495C>A | synonymous_variant | 0.12 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918482 | c.543G>T | synonymous_variant | 0.11 |
katG | 2155596 | c.516G>A | synonymous_variant | 0.12 |
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 |
ahpC | 2726725 | p.Trp178* | stop_gained | 0.18 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
folC | 2747552 | p.Gly16Asp | missense_variant | 0.11 |
thyX | 3067589 | c.357G>T | synonymous_variant | 0.18 |
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 |
rpoA | 3877649 | p.Arg287Cys | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
clpC1 | 4039939 | p.Val256Leu | missense_variant | 0.11 |
embC | 4242056 | p.Pro732Thr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246569 | p.Ala19Asp | missense_variant | 0.19 |
aftB | 4268009 | c.828G>T | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |