Run ID: ERR2229042
Sample name:
Date: 31-03-2023 16:33:46
Number of reads: 1200818
Percentage reads mapped: 98.97
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 | Drugs |
---|---|---|---|---|---|
katG | 2155137 | c.974delC | frameshift_variant | 0.11 | isoniazid, isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
ccsA | 620667 | p.Trp259* | stop_gained | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.25 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.22 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.2 |
mmpL5 | 777136 | p.Met449Leu | missense_variant | 0.18 |
mmpL5 | 777173 | c.1308C>T | synonymous_variant | 0.15 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.15 |
mmpL5 | 777191 | c.1290C>A | synonymous_variant | 0.18 |
mmpL5 | 777196 | p.Glu429Gln | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304333 | p.Ser468Asn | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.13 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.4 |
fabG1 | 1673491 | p.Val18Ile | missense_variant | 0.13 |
rpsA | 1834421 | p.Gly294Trp | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102450 | p.Lys198Met | missense_variant | 0.16 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.44 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518409 | p.Gly99Cys | missense_variant | 0.14 |
kasA | 2518933 | c.819C>T | synonymous_variant | 0.15 |
Rv2752c | 3065823 | c.369G>A | synonymous_variant | 0.12 |
Rv2752c | 3066159 | c.33G>A | synonymous_variant | 0.13 |
fbiD | 3339486 | c.369G>A | synonymous_variant | 0.13 |
fprA | 3474144 | p.Trp46Cys | missense_variant | 0.17 |
fprA | 3474529 | p.Arg175Cys | missense_variant | 0.12 |
rpoA | 3877467 | c.1041T>C | synonymous_variant | 0.13 |
clpC1 | 4038220 | p.Glu829Lys | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.24 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.27 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.31 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.31 |
embB | 4246747 | p.Asp78Glu | missense_variant | 0.29 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |