Run ID: SRR4035931
Sample name:
Date: 04-04-2023 07:23:15
Number of reads: 1186979
Percentage reads mapped: 99.69
Strain: lineage4.4.1.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
lineage4.4.1.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2153990 | c.2121delT | frameshift_variant | 0.25 | isoniazid |
katG | 2154793 | c.1318dupG | frameshift_variant | 0.11 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5704 | c.465C>A | synonymous_variant | 0.14 |
gyrB | 7185 | p.Ser649Tyr | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8524 | c.1225delC | frameshift_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9617 | c.2316C>T | synonymous_variant | 0.12 |
mshA | 576073 | c.726C>T | synonymous_variant | 0.15 |
mmpL5 | 775597 | p.Ala962Ser | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.17 |
fbiC | 1304074 | p.Ala382Thr | missense_variant | 0.13 |
embR | 1416929 | p.Ala140Val | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472204 | n.359G>T | non_coding_transcript_exon_variant | 0.25 |
inhA | 1674534 | c.333G>A | synonymous_variant | 0.12 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.12 |
rpsA | 1834716 | c.1179dupC | frameshift_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.33 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.25 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714224 | p.Ala370Val | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
fbiB | 3640683 | c.-852C>T | upstream_gene_variant | 0.15 |
panD | 4044179 | p.Ala35Thr | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242748 | c.-485A>C | upstream_gene_variant | 0.14 |
embB | 4246928 | p.Gln139Lys | missense_variant | 0.12 |
embB | 4247161 | c.648G>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |