Run ID: ERR5866287
Sample name:
Date: 02-04-2023 00:36:25
Number of reads: 620649
Percentage reads mapped: 98.74
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288817 | p.Thr142Met | missense_variant | 0.75 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8072 | c.772delG | frameshift_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 619914 | c.24C>T | synonymous_variant | 0.17 |
rpoC | 764196 | p.Ser276* | stop_gained | 0.22 |
rpoC | 764918 | p.Val517Leu | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775994 | c.2487C>T | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 1.0 |
atpE | 1461203 | c.159C>T | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1833813 | p.Leu91His | missense_variant | 0.12 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 0.93 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
katG | 2156475 | c.-364A>T | upstream_gene_variant | 0.1 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.2 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.2 |
Rv1979c | 2223044 | p.Gly41Arg | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449534 | p.Thr344Ile | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 0.11 |
alr | 3840712 | p.Ser237Pro | missense_variant | 0.1 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
embC | 4240682 | p.Asp274Asn | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244001 | p.Val257Met | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407857 | p.Arg116Trp | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |