Run ID: ERR2229355
Sample name:
Date: 18-08-2022 10:31:21
Number of reads: 1275494
Percentage reads mapped: 97.81
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5672 | p.Glu145Lys | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9660 | p.Ala787Ser | missense_variant | 0.15 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
rpoB | 762125 | c.2321_2322dupTG | frameshift_variant | 0.13 |
rpoC | 763582 | p.Lys71Asn | missense_variant | 0.13 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.12 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.17 |
rpoC | 765768 | p.Ile800Thr | missense_variant | 0.12 |
mmpR5 | 779320 | p.Met111Leu | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303110 | c.181delA | frameshift_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304497 | p.Pro523Ser | missense_variant | 0.12 |
embR | 1417377 | c.-30C>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471822 | n.-24C>A | upstream_gene_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476291 | n.2634G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476780 | n.3123C>A | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.17 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.17 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.19 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.47 |
fabG1 | 1673439 | c.-1G>T | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155191 | c.921A>C | synonymous_variant | 0.15 |
katG | 2155515 | c.597C>A | synonymous_variant | 0.12 |
kasA | 2517964 | c.-151C>T | upstream_gene_variant | 0.15 |
kasA | 2518839 | p.Ala242Gly | missense_variant | 0.14 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.12 |
eis | 2714223 | c.1110C>A | synonymous_variant | 0.17 |
folC | 2747011 | c.588G>T | synonymous_variant | 0.17 |
ribD | 2986809 | c.-30G>T | upstream_gene_variant | 0.17 |
ribD | 2987330 | c.492G>T | synonymous_variant | 0.15 |
thyX | 3067345 | p.Ser201Cys | missense_variant | 0.13 |
thyX | 3067367 | c.579G>A | synonymous_variant | 0.14 |
thyX | 3068015 | c.-70T>G | upstream_gene_variant | 0.2 |
ald | 3087059 | c.240G>A | synonymous_variant | 0.12 |
ald | 3087279 | p.Gly154Trp | missense_variant | 0.2 |
fbiA | 3640476 | c.-67C>A | upstream_gene_variant | 0.15 |
fbiA | 3641267 | p.Gly242Val | missense_variant | 0.12 |
fbiB | 3642039 | p.Gly169Ser | missense_variant | 0.14 |
fbiB | 3642272 | c.738C>A | synonymous_variant | 0.13 |
fbiB | 3642698 | c.1164G>A | synonymous_variant | 0.14 |
alr | 3840209 | p.Glu404Asp | missense_variant | 0.13 |
alr | 3840619 | p.Asp268His | missense_variant | 0.13 |
alr | 3840661 | p.Gly254Cys | missense_variant | 0.2 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.16 |
embC | 4240883 | p.Ser341Arg | missense_variant | 0.17 |
embC | 4241601 | p.Met580Lys | missense_variant | 0.18 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.19 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.57 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.65 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.65 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.36 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.33 |
embB | 4248783 | p.Pro757His | missense_variant | 0.17 |
ethA | 4326166 | c.1308A>G | synonymous_variant | 0.17 |
ethA | 4326195 | p.Glu427Gln | missense_variant | 0.11 |
ethA | 4327184 | p.His97Arg | missense_variant | 0.12 |