Run ID: ERR11050349
Sample name:
Date: 03-04-2023 00:03:25
Number of reads: 5405073
Percentage reads mapped: 99.55
Strain: lineage4.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 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 | 8694 | c.1393C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.15 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.31 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.2 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.2 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.3 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.24 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.17 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.99 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.24 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.26 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.24 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.2 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.18 |
Rv2752c | 3065462 | p.Arg244Trp | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.43 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475346 | p.Leu447Arg | missense_variant | 1.0 |
Rv3236c | 3612515 | p.Arg201His | missense_variant | 1.0 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.5 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.18 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.67 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.36 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.34 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.18 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408031 | p.Leu58Phe | missense_variant | 1.0 |