Run ID: ERR2229117
Sample name:
Date: 31-03-2023 16:42:05
Number of reads: 1511579
Percentage reads mapped: 99.5
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575555 | p.Val70Phe | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.31 |
rpoC | 764351 | p.Val328Met | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407530 | c.-190A>G | upstream_gene_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474975 | n.1318G>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.16 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.16 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
inhA | 1674962 | c.764delG | frameshift_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.12 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.24 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519183 | p.Leu357Ile | missense_variant | 0.12 |
ribD | 2987302 | p.Arg155Leu | missense_variant | 0.12 |
ribD | 2987419 | p.Gly194Val | missense_variant | 0.17 |
Rv2752c | 3064628 | p.Asn522Asp | missense_variant | 0.17 |
ald | 3087235 | p.Arg139Leu | missense_variant | 0.14 |
ald | 3087819 | c.1000C>A | synonymous_variant | 0.17 |
fbiB | 3641956 | p.Gly141Asp | missense_variant | 0.12 |
fbiB | 3641966 | c.432C>A | synonymous_variant | 0.13 |
fbiB | 3641997 | p.Ala155Ser | missense_variant | 0.12 |
fbiB | 3642043 | p.Leu170Pro | missense_variant | 0.17 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
panD | 4044274 | p.Arg3Leu | missense_variant | 0.12 |
panD | 4044285 | c.-4A>G | upstream_gene_variant | 0.12 |
panD | 4044322 | c.-41G>A | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244598 | p.Leu456Met | missense_variant | 0.11 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.18 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.18 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.18 |
embB | 4246567 | c.54G>T | synonymous_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 |