Run ID: ERR2229090
Sample name:
Date: 31-03-2023 16:37:47
Number of reads: 698270
Percentage reads mapped: 99.46
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
tlyA | 1918517 | c.582delC | frameshift_variant | 0.12 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7398 | p.Met33Leu | missense_variant | 0.13 |
mshA | 575862 | p.Pro172Gln | missense_variant | 0.11 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
mshA | 576114 | p.Arg256Pro | missense_variant | 0.22 |
rpoB | 759914 | c.108T>C | synonymous_variant | 0.1 |
rpoB | 761569 | p.Ile588Asn | missense_variant | 0.18 |
rpoB | 761926 | p.Met707Thr | missense_variant | 0.12 |
rpoC | 763551 | p.Tyr61Cys | missense_variant | 0.1 |
rpoC | 765262 | c.1893C>G | synonymous_variant | 0.12 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776032 | p.Gly817Trp | missense_variant | 0.2 |
mmpL5 | 776751 | p.Phe577Tyr | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303367 | p.Thr146Asn | missense_variant | 0.12 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.25 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416565 | p.Asp261Glu | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473029 | n.1184C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473498 | n.-160G>T | upstream_gene_variant | 0.18 |
rrl | 1473714 | n.57C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673416 | c.-24G>A | upstream_gene_variant | 0.17 |
rpsA | 1833526 | c.-16G>T | upstream_gene_variant | 0.12 |
rpsA | 1834052 | p.Ala171Ser | missense_variant | 0.12 |
tlyA | 1917941 | p.Val1Ala | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918205 | p.Ala89Glu | missense_variant | 0.15 |
ndh | 2102188 | c.855G>A | synonymous_variant | 0.2 |
ndh | 2103056 | c.-14A>T | upstream_gene_variant | 0.18 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.53 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.12 |
Rv1979c | 2222243 | p.Ala308Ser | missense_variant | 0.15 |
Rv1979c | 2222286 | c.879G>T | synonymous_variant | 0.17 |
Rv1979c | 2222876 | c.288delC | frameshift_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289239 | c.3G>A | start_lost | 0.13 |
kasA | 2518445 | p.Val111Ile | missense_variant | 0.13 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.2 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.2 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.18 |
pepQ | 2860226 | p.Ala65Ser | missense_variant | 0.17 |
pepQ | 2860584 | c.-166C>T | upstream_gene_variant | 0.17 |
pepQ | 2860601 | c.-183C>A | upstream_gene_variant | 0.12 |
ribD | 2987136 | p.Val100Ile | missense_variant | 0.14 |
Rv2752c | 3065419 | p.Arg258Leu | missense_variant | 0.15 |
alr | 3840533 | c.888G>T | synonymous_variant | 0.15 |
rpoA | 3877572 | c.936G>T | synonymous_variant | 0.13 |
clpC1 | 4038301 | p.Val802Ile | missense_variant | 0.12 |
clpC1 | 4039162 | p.His515Asn | missense_variant | 0.13 |
embC | 4241143 | c.1281C>A | synonymous_variant | 0.13 |
embC | 4241960 | c.2098C>T | synonymous_variant | 0.29 |
embC | 4242086 | p.Gln742* | stop_gained | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244144 | c.912C>T | synonymous_variant | 0.18 |
embB | 4246196 | c.-318C>T | upstream_gene_variant | 0.22 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.5 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.5 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.14 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.14 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.14 |
ethA | 4327483 | c.-10G>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |