Run ID: ERR2229343
Sample name:
Date: 31-03-2023 17:04:49
Number of reads: 1420281
Percentage reads mapped: 98.98
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6399 | p.Val387Ala | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.15 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.22 |
ccsA | 620262 | c.372C>T | synonymous_variant | 0.15 |
ccsA | 620268 | c.378G>T | synonymous_variant | 0.15 |
ccsA | 620438 | p.Ser183Tyr | missense_variant | 0.12 |
ccsA | 620472 | p.Ile194Met | missense_variant | 0.14 |
rpoC | 764233 | c.866delA | frameshift_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776145 | p.Ala779Asp | missense_variant | 0.21 |
mmpL5 | 778086 | c.394delG | frameshift_variant | 0.15 |
mmpS5 | 779597 | c.-693delA | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406353 | p.Pro330Thr | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472208 | n.363A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475467 | n.1810G>T | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.35 |
fabG1 | 1674178 | c.740delA | frameshift_variant | 0.15 |
inhA | 1674948 | p.Trp249* | stop_gained | 0.14 |
rpsA | 1833355 | c.-187C>A | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102714 | c.328delA | frameshift_variant | 0.12 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.21 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.28 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.28 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.31 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.12 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.7 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.72 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.13 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518197 | p.Asp28Ala | missense_variant | 0.17 |
kasA | 2518200 | p.Ile29Asn | missense_variant | 0.17 |
kasA | 2518201 | c.88delG | frameshift_variant | 0.18 |
kasA | 2518218 | p.Gly35Ala | missense_variant | 0.19 |
kasA | 2518226 | p.Ala38Ser | missense_variant | 0.21 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.19 |
kasA | 2519187 | p.Thr358Met | missense_variant | 0.18 |
kasA | 2519330 | p.Gly406Ser | missense_variant | 0.12 |
Rv2752c | 3066081 | c.111G>T | synonymous_variant | 0.22 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 1.0 |
whiB7 | 3568418 | c.250_261delGGACGTCCGCGC | conservative_inframe_deletion | 0.12 |
fbiB | 3642673 | p.Ala380Gly | missense_variant | 0.17 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.24 |
rpoA | 3878599 | c.-92C>G | upstream_gene_variant | 0.67 |
clpC1 | 4039071 | p.Pro545Gln | missense_variant | 0.15 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242686 | p.Gln942Lys | missense_variant | 0.4 |
embA | 4244184 | p.Ser318Arg | missense_variant | 0.15 |
embA | 4244522 | c.1290C>A | synonymous_variant | 0.2 |
embB | 4246283 | c.-231G>A | upstream_gene_variant | 0.18 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.24 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.62 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.58 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.58 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.25 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.13 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |