Run ID: SRR6785457
Sample name:
Date: 04-04-2023 15:57:17
Number of reads: 859936
Percentage reads mapped: 99.56
Strain: lineage4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | 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 | 8286 | p.Asn329Tyr | missense_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 1.0 |
fgd1 | 491352 | c.570C>T | synonymous_variant | 0.5 |
fgd1 | 491595 | c.813C>T | synonymous_variant | 0.25 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.25 |
mshA | 576531 | p.Val395Asp | missense_variant | 0.2 |
rpoC | 764993 | p.Ala542Ser | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776582 | p.Gln633His | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472084 | n.239C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.53 |
fabG1 | 1673807 | p.Ala123Glu | missense_variant | 0.25 |
fabG1 | 1673927 | p.Met163Thr | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170308 | p.Leu102Ala | missense_variant | 1.0 |
PPE35 | 2170313 | c.300G>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.14 |
pepQ | 2859678 | c.741A>T | synonymous_variant | 0.23 |
ribD | 2986910 | c.72C>A | synonymous_variant | 1.0 |
Rv2752c | 3065440 | p.Ala251Asp | missense_variant | 0.22 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840689 | c.732C>T | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
embB | 4249647 | p.Arg1045Leu | missense_variant | 0.17 |
aftB | 4267338 | p.Leu500Pro | missense_variant | 0.17 |
aftB | 4269468 | c.-632G>A | upstream_gene_variant | 0.25 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
PPE35 | 2167025 | c.336_*623del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |