Run ID: ERR4812126
Sample name:
Date: 01-04-2023 11:52:41
Number of reads: 667279
Percentage reads mapped: 99.47
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.31 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 0.54 | isoniazid, ethionamide |
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 | 0.35 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.38 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.43 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.33 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.25 |
rpoB | 761889 | p.Val695Leu | missense_variant | 0.59 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.37 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801009 | c.201A>G | synonymous_variant | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102404 | c.639G>A | synonymous_variant | 0.12 |
ndh | 2102456 | p.Thr196Lys | missense_variant | 0.15 |
ndh | 2102521 | c.522C>A | synonymous_variant | 0.15 |
Rv1979c | 2223214 | c.-50A>C | upstream_gene_variant | 0.48 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.39 |
Rv2752c | 3065517 | c.675C>T | synonymous_variant | 0.59 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.35 |
Rv3083 | 3448439 | c.-64delA | upstream_gene_variant | 0.72 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.25 |
fprA | 3474299 | p.Asp98Gly | missense_variant | 0.62 |
clpC1 | 4040211 | p.Pro165Gln | missense_variant | 0.15 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.67 |
embC | 4242806 | p.Phe982Ile | missense_variant | 0.67 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.29 |
embB | 4248041 | p.Ala510Ser | missense_variant | 0.12 |
ethA | 4326996 | p.Pro160Thr | missense_variant | 0.67 |
ethA | 4328317 | c.-844C>T | upstream_gene_variant | 0.39 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408365 | c.-163C>T | upstream_gene_variant | 0.12 |