Run ID: ERR4407460
Sample name:
Date: 01-04-2023 05:45:00
Number of reads: 355238
Percentage reads mapped: 99.57
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6591 | p.Arg451Leu | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8703 | p.Ile468Val | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575176 | c.-172T>G | upstream_gene_variant | 0.18 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575947 | c.600G>A | synonymous_variant | 0.12 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.36 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760563 | c.757C>A | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778871 | p.Leu12Pro | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406917 | p.Ile142Val | missense_variant | 0.1 |
atpE | 1460979 | c.-66G>A | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155079 | p.Lys345* | stop_gained | 0.12 |
katG | 2155855 | p.Thr86Ser | missense_variant | 0.13 |
Rv1979c | 2221928 | p.Thr413Ala | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714360 | p.Asp325Asn | missense_variant | 0.15 |
pepQ | 2859393 | c.1026G>A | synonymous_variant | 0.13 |
Rv2752c | 3064747 | p.Gly482Asp | missense_variant | 0.12 |
thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.2 |
fbiD | 3339500 | c.385dupA | frameshift_variant | 0.17 |
Rv3083 | 3448918 | p.Cys139Arg | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878555 | c.-48G>C | upstream_gene_variant | 1.0 |
embC | 4241836 | c.1974A>T | synonymous_variant | 0.18 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
ubiA | 4269022 | p.Ala271Val | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |