Run ID: SRR7517800
Sample name:
Date: 04-04-2023 19:39:20
Number of reads: 1786816
Percentage reads mapped: 99.66
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 | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761889 | p.Val695Leu | missense_variant | 1.0 |
rpoC | 763826 | p.Ala153Ser | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801009 | c.201A>G | synonymous_variant | 1.0 |
Rv1258c | 1406682 | p.Trp220* | stop_gained | 1.0 |
embR | 1416891 | p.Leu153Val | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475488 | n.1831G>A | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917955 | p.Arg6Cys | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.55 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.6 |
Rv1979c | 2223214 | c.-50A>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065517 | c.675C>T | synonymous_variant | 1.0 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.11 |
thyX | 3067613 | p.Glu111Asp | missense_variant | 0.12 |
ald | 3086772 | c.-48A>G | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
fprA | 3474299 | p.Asp98Gly | missense_variant | 1.0 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.29 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.16 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.12 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.12 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.1 |
ethA | 4328317 | c.-844C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |