Run ID: SRR6785288
Sample name:
Date: 04-04-2023 15:42:24
Number of reads: 1038908
Percentage reads mapped: 99.79
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 |
---|---|---|---|---|
gyrB | 7067 | p.Tyr610Asp | missense_variant | 0.18 |
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 | 8114 | c.813C>T | synonymous_variant | 0.25 |
gyrA | 8527 | p.Arg409Gln | missense_variant | 1.0 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491257 | p.Gly159Cys | missense_variant | 0.4 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
rpoC | 762455 | c.-915C>T | upstream_gene_variant | 0.17 |
rpoC | 764543 | p.Thr392Pro | missense_variant | 0.15 |
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 | 1303095 | c.165G>A | synonymous_variant | 1.0 |
Rv1258c | 1406873 | c.468C>A | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.3 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.3 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.2 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.2 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.2 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.33 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
PPE35 | 2168133 | p.Asp827Ala | missense_variant | 0.4 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.38 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
thyX | 3067654 | p.His98Asn | missense_variant | 0.2 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449102 | p.Asn200Thr | missense_variant | 0.43 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474507 | c.501C>G | synonymous_variant | 1.0 |
fprA | 3475268 | p.Ala421Val | missense_variant | 0.57 |
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 |
embA | 4244982 | p.Leu584Val | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408174 | p.Ala10Gly | missense_variant | 1.0 |