Run ID: SRR8420472
Sample name:
Date: 04-04-2023 21:22:52
Number of reads: 1680943
Percentage reads mapped: 99.61
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 0.99 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778094 | c.-896A>G | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406486 | c.855T>C | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.13 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.12 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.16 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.19 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.16 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.11 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.14 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.3 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.32 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519076 | p.Ala321Val | missense_variant | 0.15 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.12 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.12 |
thyA | 3074580 | c.-109T>C | upstream_gene_variant | 0.23 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3449041 | p.Val180Ile | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612155 | p.Arg321Leu | missense_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
Rv3236c | 3612895 | c.222T>C | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243096 | c.-137A>C | upstream_gene_variant | 0.11 |
embA | 4243099 | c.-134G>C | upstream_gene_variant | 0.12 |
embA | 4243102 | c.-131G>T | upstream_gene_variant | 0.11 |
embC | 4243103 | p.Thr1081Pro | missense_variant | 0.11 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.16 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.15 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |