Run ID: SRR3732702
Sample name:
Date: 04-04-2023 05:38:04
Number of reads: 169435
Percentage reads mapped: 98.86
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491190 | c.408G>T | synonymous_variant | 0.67 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
rpoB | 760240 | p.Thr145Met | missense_variant | 0.5 |
rpoB | 760272 | p.Glu156Lys | missense_variant | 0.33 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
rpoB | 762683 | p.Glu959Asp | missense_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765820 | c.2451G>T | synonymous_variant | 1.0 |
mmpL5 | 777695 | c.786G>T | synonymous_variant | 1.0 |
fbiC | 1303616 | p.Ala229Val | missense_variant | 1.0 |
fbiC | 1304853 | c.1923C>A | synonymous_variant | 0.67 |
fbiC | 1305187 | p.Leu753Met | missense_variant | 0.5 |
Rv1258c | 1406228 | c.1113C>A | synonymous_variant | 0.4 |
embR | 1416201 | p.Gly383Trp | missense_variant | 0.67 |
rrl | 1473729 | n.72T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474150 | n.493C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476596 | n.2939C>A | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833768 | p.Pro76His | missense_variant | 1.0 |
tlyA | 1917828 | c.-112G>T | upstream_gene_variant | 0.67 |
katG | 2155269 | c.843C>A | synonymous_variant | 1.0 |
PPE35 | 2168776 | p.Pro613Thr | missense_variant | 1.0 |
PPE35 | 2169099 | p.Gly505Val | missense_variant | 1.0 |
Rv1979c | 2222555 | p.Pro204Thr | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289415 | c.-174C>A | upstream_gene_variant | 0.33 |
ahpC | 2726016 | c.-177C>T | upstream_gene_variant | 0.33 |
ahpC | 2726642 | c.450C>A | synonymous_variant | 0.67 |
folC | 2746828 | c.771C>A | synonymous_variant | 0.5 |
pepQ | 2860200 | c.219G>T | synonymous_variant | 1.0 |
ribD | 2987294 | c.456G>T | synonymous_variant | 1.0 |
Rv2752c | 3065549 | p.Glu215* | stop_gained | 1.0 |
thyX | 3067888 | p.Pro20Thr | missense_variant | 0.67 |
ald | 3086997 | p.Thr60Gly | missense_variant | 1.0 |
Rv3083 | 3449058 | c.555C>T | synonymous_variant | 0.5 |
Rv3083 | 3449501 | p.Ser333Tyr | missense_variant | 0.29 |
fprA | 3474468 | c.462C>A | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640364 | c.-179G>T | upstream_gene_variant | 0.4 |
fbiB | 3642214 | p.Ser227Leu | missense_variant | 1.0 |
fbiB | 3642523 | p.Ala330Val | missense_variant | 1.0 |
alr | 3841307 | c.114C>A | synonymous_variant | 0.5 |
rpoA | 3877751 | p.Asp253Tyr | missense_variant | 0.33 |
embC | 4241927 | p.Arg689* | stop_gained | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4245824 | c.-690G>A | upstream_gene_variant | 1.0 |
embB | 4248136 | c.1623C>T | synonymous_variant | 0.5 |
aftB | 4267781 | c.1056C>A | synonymous_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |