Run ID: ERR4815975
Sample name:
Date: 01-04-2023 14:10:15
Number of reads: 548709
Percentage reads mapped: 99.31
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 | 8382 | p.Leu361Met | missense_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491734 | p.Arg318Ser | missense_variant | 0.13 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777281 | c.1199delT | frameshift_variant | 0.17 |
mmpL5 | 777538 | c.943C>T | synonymous_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781589 | p.Lys10Asn | missense_variant | 0.14 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673467 | p.Lys10Glu | missense_variant | 0.12 |
fabG1 | 1673855 | p.Gly139Val | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918636 | p.Pro233Thr | missense_variant | 0.15 |
ndh | 2102256 | p.Asp263Asn | missense_variant | 0.17 |
ndh | 2102268 | p.Val259Ile | missense_variant | 0.13 |
ndh | 2102506 | c.537C>T | synonymous_variant | 1.0 |
PPE35 | 2169934 | p.Ile227Phe | missense_variant | 0.14 |
PPE35 | 2170256 | c.357G>T | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289330 | c.-89G>A | upstream_gene_variant | 0.1 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518803 | p.Phe230Ser | missense_variant | 0.15 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448982 | p.Gly160Val | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641127 | c.-408T>C | upstream_gene_variant | 0.11 |
rpoA | 3878237 | p.Glu91Lys | missense_variant | 0.12 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.12 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.12 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.12 |
clpC1 | 4040453 | c.252C>A | synonymous_variant | 0.15 |
clpC1 | 4040708 | c.-4A>G | upstream_gene_variant | 0.33 |
embC | 4241225 | p.Pro455Ser | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242881 | p.Pro1007Thr | missense_variant | 0.12 |
embA | 4245786 | p.Ala852Thr | missense_variant | 1.0 |
embA | 4246015 | p.Pro928Leu | missense_variant | 0.14 |
embB | 4246040 | c.-474C>T | upstream_gene_variant | 0.13 |
embB | 4247260 | c.747C>A | synonymous_variant | 0.13 |
embB | 4247547 | p.Asp345Gly | missense_variant | 0.18 |
embB | 4247551 | c.1038C>T | synonymous_variant | 0.18 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.29 |
aftB | 4267520 | c.1317T>C | synonymous_variant | 0.17 |
aftB | 4268642 | p.Tyr65* | stop_gained | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |