Run ID: SRR18715394
Sample name:
Date: 03-04-2023 20:32:19
Number of reads: 2739302
Percentage reads mapped: 99.65
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6988 | c.-314C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491693 | p.Gly304Asp | missense_variant | 1.0 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.42 |
ccsA | 620619 | c.729G>A | synonymous_variant | 1.0 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.28 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.29 |
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 | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289302 | c.-61C>T | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.27 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.12 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474077 | p.Lys24Thr | missense_variant | 0.19 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.33 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.3 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.62 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245835 | p.Leu868Arg | missense_variant | 0.21 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.3 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.12 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.12 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.45 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.25 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.24 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.21 |
ethA | 4327310 | p.Ser55Cys | missense_variant | 1.0 |
ethA | 4327412 | p.Trp21Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |