Run ID: ERR4819624
Sample name:
Date: 01-04-2023 16:12:58
Number of reads: 817498
Percentage reads mapped: 99.47
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 | 0.99 |
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 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777623 | c.858G>A | synonymous_variant | 0.14 |
mmpL5 | 777626 | c.855C>T | synonymous_variant | 0.14 |
mmpL5 | 777637 | p.Ile282Val | missense_variant | 0.12 |
mmpL5 | 777647 | c.834C>G | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407215 | c.126G>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833376 | c.-166C>A | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.18 |
PPE35 | 2169305 | p.Asp436Glu | missense_variant | 0.11 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.2 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.2 |
PPE35 | 2170357 | p.Ala86Thr | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517937 | c.-178G>T | upstream_gene_variant | 0.1 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746734 | p.Ile289Val | missense_variant | 0.15 |
Rv2752c | 3066231 | c.-40G>T | upstream_gene_variant | 0.15 |
thyX | 3067679 | c.267C>T | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840338 | c.1083C>T | synonymous_variant | 0.12 |
clpC1 | 4039161 | p.His515Gly | missense_variant | 0.13 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.12 |
embC | 4240712 | p.Trp284Arg | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249293 | p.Lys927Arg | missense_variant | 1.0 |
aftB | 4269261 | c.-425G>A | upstream_gene_variant | 0.22 |
ethA | 4327896 | c.-423C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408453 | c.-251G>A | upstream_gene_variant | 1.0 |