Run ID: ERR11049963
Sample name:
Date: 02-04-2023 05:05:09
Number of reads: 3903435
Percentage reads mapped: 99.65
Strain: lineage4.3.4.1
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 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.1 | Euro-American (LAM) | LAM1;LAM2 | RD174 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.21 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.25 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.3 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.27 |
mshA | 576606 | p.Ala420Gly | missense_variant | 0.17 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.28 |
rpoB | 759608 | c.-199C>T | upstream_gene_variant | 1.0 |
rpoB | 763151 | p.Phe1115Leu | missense_variant | 0.18 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.27 |
rpoC | 764534 | p.Arg389Gly | missense_variant | 0.19 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801066 | c.258G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.36 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154425 | p.Ile563Val | missense_variant | 1.0 |
PPE35 | 2169960 | p.Gly218Asp | missense_variant | 1.0 |
PPE35 | 2170037 | c.576C>G | synonymous_variant | 0.29 |
PPE35 | 2170041 | p.Thr191Arg | missense_variant | 0.19 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.34 |
ahpC | 2726323 | p.Pro44Arg | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.24 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.25 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.18 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.33 |
Rv3083 | 3448598 | p.Ile32Thr | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.29 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.43 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
rpoA | 3878494 | p.Gln5Arg | missense_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.65 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.44 |
embC | 4240427 | p.Ser189Cys | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.54 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.25 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.19 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |