Run ID: ERR2229317
Sample name:
Date: 31-03-2023 17:01:39
Number of reads: 1280989
Percentage reads mapped: 98.48
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491407 | p.Pro209Thr | missense_variant | 0.4 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mshA | 576289 | c.942G>C | synonymous_variant | 0.22 |
ccsA | 620795 | p.Ala302Val | missense_variant | 0.12 |
rpoC | 765517 | c.2148C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775850 | p.Ser877Arg | missense_variant | 0.25 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417340 | p.Gly3Val | missense_variant | 0.13 |
embR | 1417358 | c.-11G>T | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475674 | n.2017A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476627 | n.2970G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476667 | n.3010T>A | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.34 |
fabG1 | 1673862 | c.424delT | frameshift_variant | 0.17 |
rpsA | 1834450 | p.Lys303Asn | missense_variant | 0.25 |
rpsA | 1834851 | p.Ala437Val | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.2 |
PPE35 | 2167762 | p.Ser951Pro | missense_variant | 0.15 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.15 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.15 |
PPE35 | 2168047 | p.Leu856Val | missense_variant | 0.11 |
PPE35 | 2168235 | p.Ala793Glu | missense_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.12 |
PPE35 | 2169725 | c.888T>C | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.64 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.65 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518209 | p.Thr32Lys | missense_variant | 0.12 |
ribD | 2987006 | c.170delG | frameshift_variant | 0.33 |
Rv2752c | 3064795 | p.Leu466Pro | missense_variant | 0.14 |
thyX | 3068015 | c.-70T>G | upstream_gene_variant | 0.11 |
fbiD | 3339736 | p.Thr207Pro | missense_variant | 0.18 |
Rv3236c | 3612997 | c.120T>C | synonymous_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.11 |
panD | 4044395 | c.-114C>A | upstream_gene_variant | 0.14 |
panD | 4044404 | c.-123G>A | upstream_gene_variant | 0.13 |
embC | 4241616 | p.Lys585Arg | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244665 | p.Thr478Arg | missense_variant | 0.14 |
embA | 4244720 | c.1488C>T | synonymous_variant | 0.15 |
embA | 4244918 | c.1686G>T | synonymous_variant | 0.18 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.19 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.44 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.46 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.46 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.21 |
ubiA | 4269479 | p.Met119Leu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |