Run ID: ERR973458
Sample name:
Date: 02-04-2023 12:03:07
Number of reads: 124385
Percentage reads mapped: 99.55
Strain: lineage4
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4327132 | c.341delA | frameshift_variant | 0.75 | ethionamide, 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 |
mshA | 575532 | p.Thr62Ser | missense_variant | 0.5 |
mshA | 576460 | c.1118_1120delCGG | disruptive_inframe_deletion | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765796 | c.2427C>G | synonymous_variant | 0.33 |
rpoC | 767111 | p.Leu1248Met | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304566 | p.Phe546Val | missense_variant | 0.4 |
Rv1258c | 1406350 | p.Ile331Leu | missense_variant | 0.25 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.29 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.29 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.29 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.29 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.29 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.5 |
katG | 2154869 | p.Leu415Met | missense_variant | 1.0 |
katG | 2155844 | p.Trp90Arg | missense_variant | 1.0 |
PPE35 | 2169708 | p.Thr302Asn | missense_variant | 0.4 |
PPE35 | 2169925 | c.679_687delATCGGCAAC | conservative_inframe_deletion | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289151 | p.Ile31Phe | missense_variant | 1.0 |
ahpC | 2726149 | c.-44T>C | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086948 | c.129G>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
panD | 4044344 | c.-63T>G | upstream_gene_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247978 | p.Ile489Leu | missense_variant | 0.4 |
embB | 4249734 | p.Pro1074Leu | missense_variant | 1.0 |
aftB | 4269324 | c.-488C>T | upstream_gene_variant | 0.5 |
ubiA | 4270004 | c.-171G>T | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407928 | p.Glu92Ala | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408271 | c.-69A>G | upstream_gene_variant | 0.67 |