Run ID: DRR034504
Sample name:
Date: 31-03-2023 07:00:50
Number of reads: 1172061
Percentage reads mapped: 98.8
Strain: lineage4.2.2
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 | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7121 | p.Pro628Ala | missense_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 | 576077 | c.730C>T | synonymous_variant | 1.0 |
ccsA | 620563 | p.Leu225Met | missense_variant | 0.13 |
ccsA | 620858 | p.Val323Ala | missense_variant | 0.11 |
rpoC | 766381 | c.3013delG | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | 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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518447 | c.333T>G | synonymous_variant | 0.12 |
kasA | 2519234 | p.Glu374* | stop_gained | 0.15 |
folC | 2746147 | c.1452T>A | synonymous_variant | 0.12 |
folC | 2746153 | p.Phe482Leu | missense_variant | 0.12 |
folC | 2746246 | c.1353C>T | synonymous_variant | 0.12 |
pepQ | 2860546 | c.-128A>G | upstream_gene_variant | 0.1 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339663 | p.Trp182* | stop_gained | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878627 | c.-120T>C | upstream_gene_variant | 0.5 |
clpC1 | 4038626 | p.Met693Ile | missense_variant | 0.13 |
embC | 4240492 | c.630G>T | synonymous_variant | 0.14 |
embA | 4242430 | c.-803C>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242819 | p.Leu986Pro | missense_variant | 0.18 |
embA | 4243078 | c.-155C>G | upstream_gene_variant | 0.11 |
embC | 4243082 | c.3221_3228delATCTGAAC | frameshift_variant | 0.12 |
embC | 4243092 | p.Leu1077Arg | missense_variant | 0.12 |
embC | 4243095 | p.Gly1078Val | missense_variant | 0.12 |
embA | 4243099 | c.-134G>C | upstream_gene_variant | 0.14 |
embA | 4243102 | c.-131G>T | upstream_gene_variant | 0.14 |
embC | 4243103 | p.Thr1081Pro | missense_variant | 0.14 |
embC | 4243106 | p.Arg1082Ser | missense_variant | 0.14 |
embC | 4243107 | c.3245_3246insGTTCAGAT | frameshift_variant | 0.14 |
embA | 4243339 | p.Val36Gly | missense_variant | 0.11 |
embA | 4244400 | p.Leu390Met | missense_variant | 1.0 |
embA | 4244652 | p.Gln474Lys | missense_variant | 0.17 |
embA | 4244766 | p.Glu512Lys | missense_variant | 0.18 |
embB | 4249533 | p.Ala1007Val | missense_variant | 1.0 |
aftB | 4267766 | c.1071G>T | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |