Run ID: ERR2229271
Sample name:
Date: 31-03-2023 16:55:06
Number of reads: 1150705
Percentage reads mapped: 99.19
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 | 576100 | p.Asp251Glu | missense_variant | 0.14 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.13 |
rpoB | 762119 | c.2313C>T | synonymous_variant | 1.0 |
rpoC | 767113 | c.3744G>C | synonymous_variant | 0.11 |
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 |
embR | 1416971 | p.Ala126Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475049 | n.1392C>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.18 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.31 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714928 | c.405C>A | synonymous_variant | 0.12 |
folC | 2746261 | c.1338G>A | synonymous_variant | 0.14 |
ribD | 2987230 | p.Ala131Glu | missense_variant | 0.2 |
ribD | 2987484 | p.Ala216Ser | missense_variant | 0.14 |
ald | 3087725 | c.906C>A | synonymous_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
clpC1 | 4040411 | c.294T>G | synonymous_variant | 0.11 |
embC | 4241765 | p.Ala635Pro | missense_variant | 0.29 |
embC | 4242030 | p.Leu723Gln | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.14 |
embC | 4242773 | p.Leu971Met | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.24 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.19 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.19 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.13 |
aftB | 4267692 | p.Ile382Asn | missense_variant | 0.12 |
aftB | 4267827 | p.Arg337Gln | missense_variant | 0.25 |
aftB | 4268715 | p.Leu41Pro | missense_variant | 0.18 |
aftB | 4268731 | c.106C>A | synonymous_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |