Run ID: ERR4812622
Sample name:
Date: 01-04-2023 12:12:09
Number of reads: 889956
Percentage reads mapped: 99.56
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.46 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.23 |
mshA | 576140 | p.Glu265* | stop_gained | 0.12 |
ccsA | 620015 | p.Arg42Leu | missense_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775631 | c.2850G>A | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303146 | c.216G>A | synonymous_variant | 0.18 |
fbiC | 1304032 | p.Glu368Lys | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.97 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154271 | p.Ala614Glu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
pepQ | 2860243 | p.Arg59Gln | missense_variant | 0.12 |
Rv2752c | 3065031 | c.1161G>T | synonymous_variant | 0.11 |
Rv2752c | 3065118 | c.1074C>T | synonymous_variant | 0.89 |
thyX | 3067420 | p.Pro176Thr | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087808 | p.Arg330Leu | missense_variant | 0.11 |
fbiD | 3339519 | p.His134Gln | missense_variant | 0.12 |
fbiD | 3339617 | p.Ser167Tyr | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568818 | c.-139C>A | upstream_gene_variant | 0.11 |
alr | 3840294 | p.Ala376Val | missense_variant | 0.78 |
rpoA | 3878592 | c.-85C>A | upstream_gene_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242978 | p.Leu1039Pro | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |