Run ID: ERR11049940
Sample name:
Date: 02-04-2023 04:03:18
Number of reads: 4576240
Percentage reads mapped: 99.53
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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.18 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.17 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.22 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.33 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.25 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.13 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.21 |
rpoC | 764534 | p.Arg389Gly | missense_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.16 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.16 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.45 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.32 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.18 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.19 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyX | 3067944 | p.Val1Gly | missense_variant | 0.19 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.15 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.67 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.53 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474213 | p.Lys69Asn | missense_variant | 0.11 |
Rv3236c | 3612518 | p.Tyr200Cys | missense_variant | 1.0 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.4 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.83 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.36 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.47 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.24 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.19 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.2 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |