Run ID: SRR1002683
Sample name:
Date: 02-04-2023 14:19:38
Number of reads: 812987
Percentage reads mapped: 90.95
Strain: lineage4.2.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.99 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8033 | p.Tyr244* | stop_gained | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575210 | c.-137delG | upstream_gene_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776761 | p.Phe574Leu | missense_variant | 0.1 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.1 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102587 | c.455delT | frameshift_variant | 0.11 |
katG | 2154563 | p.Val517Phe | missense_variant | 0.12 |
PPE35 | 2169234 | p.Leu460* | stop_gained | 0.15 |
PPE35 | 2169402 | p.Thr404Met | missense_variant | 0.95 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.2 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.2 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.19 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.21 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289964 | c.-723C>A | upstream_gene_variant | 0.17 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.14 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.14 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.19 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.19 |
kasA | 2519338 | c.1224T>C | synonymous_variant | 0.11 |
folC | 2746299 | p.Glu434Lys | missense_variant | 0.15 |
folC | 2747417 | p.Gln61Arg | missense_variant | 0.11 |
thyX | 3067240 | p.Ala236Thr | missense_variant | 0.15 |
thyA | 3073941 | c.531C>T | synonymous_variant | 0.11 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4240711 | p.Trp283Cys | missense_variant | 0.12 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.17 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244934 | p.Thr568Ala | missense_variant | 0.16 |
embB | 4245722 | c.-792C>T | upstream_gene_variant | 0.14 |
embB | 4247426 | p.Gly305Thr | missense_variant | 0.13 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.17 |
aftB | 4267781 | c.1056C>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407907 | p.Glu99Gly | missense_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |