Run ID: ERR11068773
Sample name:
Date: 07-04-2023 01:19:19
Number of reads: 4167591
Percentage reads mapped: 99.42
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 |
fgd1 | 491270 | p.Tyr163Cys | missense_variant | 1.0 |
mshA | 575390 | p.Gln15Lys | missense_variant | 0.11 |
mshA | 576119 | p.Ala258Pro | missense_variant | 0.29 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471786 | n.-60T>G | upstream_gene_variant | 0.19 |
rrl | 1474571 | n.914G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154915 | c.1197A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519016 | p.Ser301Leu | missense_variant | 0.11 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.14 |
eis | 2714926 | p.Thr136Asn | missense_variant | 0.17 |
eis | 2714939 | p.Gly132Trp | missense_variant | 0.2 |
eis | 2715035 | p.Met100Val | missense_variant | 0.25 |
pepQ | 2859593 | p.Ala276Thr | missense_variant | 0.11 |
pepQ | 2859944 | p.Ala159Thr | missense_variant | 0.25 |
ribD | 2987332 | p.Cys165Tyr | missense_variant | 0.14 |
thyX | 3067342 | p.Glu202Lys | missense_variant | 0.15 |
thyX | 3067935 | p.Thr4Ile | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.18 |
clpC1 | 4038164 | c.2541G>C | synonymous_variant | 0.2 |
embC | 4241202 | p.Gly447Asp | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243919 | p.Arg229Ser | missense_variant | 0.2 |
ethR | 4327999 | p.Ala151Thr | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |