Run ID: SRR4035872
Sample name:
Date: 04-04-2023 07:21:14
Number of reads: 1202165
Percentage reads mapped: 99.62
Strain: lineage4.3.2.1
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154075 | c.2029_2036delACCTACCA | frameshift_variant | 0.11 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
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 | 576287 | c.940C>A | synonymous_variant | 0.13 |
ccsA | 620661 | c.771C>T | synonymous_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766488 | p.Pro1040Leu | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777010 | p.Pro491Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918187 | p.Gly83Asp | missense_variant | 0.18 |
katG | 2154712 | p.Leu467Ser | missense_variant | 0.12 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.36 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518792 | c.678C>T | synonymous_variant | 0.11 |
folC | 2746376 | p.Ser408* | stop_gained | 0.11 |
folC | 2747359 | c.240C>A | synonymous_variant | 0.11 |
ribD | 2986946 | c.108T>C | synonymous_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448830 | p.Trp109Cys | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.15 |
fbiB | 3641990 | p.Met152Ile | missense_variant | 0.15 |
fbiB | 3642636 | p.Ala368Thr | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4241619 | p.Trp586* | stop_gained | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243396 | p.Ile55Thr | missense_variant | 0.13 |
embB | 4247916 | p.Arg468His | missense_variant | 0.15 |
embB | 4249398 | p.Ala962Glu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407743 | p.Arg154Trp | missense_variant | 0.12 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408448 | c.-246A>G | upstream_gene_variant | 0.11 |