Run ID: ERR2229738
Sample name:
Date: 31-03-2023 17:32:26
Number of reads: 1262154
Percentage reads mapped: 99.31
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 |
rpoB | 759753 | c.-54C>A | upstream_gene_variant | 0.11 |
rpoB | 762705 | p.Ser967Ala | missense_variant | 0.25 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474091 | n.434C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474911 | n.1254G>A | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918550 | p.Arg204Pro | missense_variant | 0.19 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.25 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.12 |
Rv2752c | 3065510 | p.Gly228Cys | missense_variant | 0.12 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.15 |
Rv3236c | 3612903 | p.Ala72Ser | missense_variant | 0.12 |
alr | 3840437 | c.984G>A | synonymous_variant | 0.12 |
rpoA | 3878382 | c.126G>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.27 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.24 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.27 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.27 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.32 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
aftB | 4267895 | p.Phe314Leu | missense_variant | 0.27 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408171 | p.Ile11Asn | missense_variant | 0.78 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |