Run ID: SRR6896355
Sample name:
Date: 04-04-2023 18:03:23
Number of reads: 384035
Percentage reads mapped: 99.78
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 | 2155816 | p.Gly99Glu | missense_variant | 0.2 | isoniazid |
panD | 4043900 | p.Ala128Ser | missense_variant | 0.12 | pyrazinamide |
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 | 576634 | c.1287G>C | synonymous_variant | 0.13 |
rpoB | 760569 | p.Thr255Ala | missense_variant | 0.11 |
rpoB | 761128 | c.1326delG | frameshift_variant | 0.11 |
rpoB | 761736 | p.Ile644Val | missense_variant | 0.11 |
rpoC | 762842 | c.-528G>A | upstream_gene_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303951 | p.Asp341Tyr | missense_variant | 0.15 |
fbiC | 1304109 | c.1179C>G | synonymous_variant | 0.12 |
embR | 1416734 | c.613delG | frameshift_variant | 0.11 |
atpE | 1461129 | p.Gly29Arg | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474238 | n.581G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475201 | n.1544G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475551 | n.1894T>C | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833621 | p.Asp27Gly | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167876 | p.Gly913Cys | missense_variant | 0.12 |
Rv1979c | 2222933 | p.Ser78Pro | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289050 | c.192T>C | synonymous_variant | 0.12 |
pncA | 2289889 | c.-648C>A | upstream_gene_variant | 0.17 |
pncA | 2290188 | c.-947A>G | upstream_gene_variant | 0.12 |
ribD | 2987193 | p.Ile119Val | missense_variant | 0.13 |
ribD | 2987487 | p.Pro217Ser | missense_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074258 | c.213dupG | frameshift_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448974 | c.471C>T | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878059 | p.Val150Ala | missense_variant | 0.14 |
rpoA | 3878450 | p.Gln20* | stop_gained | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040503 | p.Gly68Ser | missense_variant | 0.12 |
embC | 4239881 | p.Pro7Thr | missense_variant | 0.33 |
embC | 4240714 | p.Trp284Cys | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245307 | c.2077delG | frameshift_variant | 0.12 |
embB | 4246490 | c.-24G>A | upstream_gene_variant | 0.12 |
embB | 4246776 | p.Val88Ala | missense_variant | 0.15 |
aftB | 4267634 | c.1203G>T | synonymous_variant | 0.14 |
aftB | 4267723 | p.Val372Phe | missense_variant | 0.13 |
aftB | 4268229 | p.Ala203Val | missense_variant | 0.11 |
aftB | 4268812 | p.Ser9Pro | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |