Run ID: ERR4407545
Sample name:
Date: 01-04-2023 05:49:21
Number of reads: 332440
Percentage reads mapped: 99.42
Strain: lineage4.2.1
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 | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6220 | c.981G>A | synonymous_variant | 0.29 |
gyrB | 6971 | p.Pro578Ser | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8429 | c.1128C>A | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576089 | c.750_769delTGATCGGCGCGCGGCCCGGG | frameshift_variant | 0.1 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.13 |
rpoC | 764543 | p.Thr392Asp | missense_variant | 0.12 |
rpoC | 765844 | c.2477delA | frameshift_variant | 0.2 |
rpoC | 765906 | c.2538delG | frameshift_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777704 | c.777G>A | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781733 | c.174G>A | synonymous_variant | 0.12 |
fbiC | 1303910 | p.Pro327Arg | missense_variant | 0.2 |
fbiC | 1303927 | p.Ala333Ser | missense_variant | 0.17 |
fbiC | 1305103 | p.Val725Leu | missense_variant | 0.12 |
fbiC | 1305334 | p.Gly802Ser | missense_variant | 0.1 |
Rv1258c | 1407310 | p.Leu11Met | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474131 | n.474C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475122 | n.1465C>A | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154439 | p.Ala558Val | missense_variant | 0.13 |
katG | 2155371 | c.741C>T | synonymous_variant | 1.0 |
PPE35 | 2168255 | c.2357delT | frameshift_variant | 0.11 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289711 | c.-470T>A | upstream_gene_variant | 0.17 |
eis | 2714757 | c.576C>A | synonymous_variant | 0.11 |
pepQ | 2860307 | p.Gly38Trp | missense_variant | 0.12 |
Rv2752c | 3064558 | p.Tyr545Phe | missense_variant | 0.25 |
thyX | 3067582 | p.Met122Val | missense_variant | 0.14 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448912 | p.Ile137Val | missense_variant | 0.33 |
Rv3083 | 3449142 | c.639C>T | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612616 | c.501G>T | synonymous_variant | 0.12 |
Rv3236c | 3612729 | p.Ser130Pro | missense_variant | 0.13 |
alr | 3840551 | c.870G>T | synonymous_variant | 0.12 |
rpoA | 3878197 | p.Glu104Gly | missense_variant | 0.12 |
clpC1 | 4038538 | p.Thr723Ala | missense_variant | 0.18 |
embC | 4241139 | p.Ala426Glu | missense_variant | 0.15 |
embC | 4241623 | c.1761C>G | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247000 | p.Gly163Trp | missense_variant | 0.11 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
embB | 4249749 | p.Glu1079Gly | missense_variant | 0.4 |
aftB | 4267478 | c.1359G>A | synonymous_variant | 0.1 |
ethA | 4326950 | p.Ala175Val | missense_variant | 0.12 |
ethA | 4327109 | p.Ser122Asn | missense_variant | 0.15 |
ethR | 4327587 | p.Arg13Ser | missense_variant | 0.18 |
ethA | 4328214 | c.-741C>T | upstream_gene_variant | 1.0 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |