Run ID: ERR2228814
Sample name:
Date: 31-03-2023 16:21:51
Number of reads: 1052990
Percentage reads mapped: 99.37
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 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.14 |
rpoB | 760155 | p.Lys117* | stop_gained | 0.31 |
rpoB | 760367 | c.561G>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779243 | p.Val85Gly | missense_variant | 0.21 |
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 |
rrs | 1472212 | n.367T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473976 | n.319T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475089 | n.1432A>T | non_coding_transcript_exon_variant | 0.23 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103230 | c.-188T>G | upstream_gene_variant | 0.21 |
katG | 2154866 | p.Ile416Phe | missense_variant | 0.2 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.21 |
PPE35 | 2168231 | c.2382T>A | synonymous_variant | 0.38 |
PPE35 | 2168452 | p.Ile721Phe | missense_variant | 0.18 |
PPE35 | 2168555 | c.2058T>C | synonymous_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169377 | p.Phe412Leu | missense_variant | 0.14 |
PPE35 | 2170263 | p.Leu117Arg | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859688 | p.Asp244Ala | missense_variant | 0.43 |
pepQ | 2859710 | p.Phe237Ile | missense_variant | 0.18 |
thyX | 3067341 | p.Glu202Ala | missense_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245624 | p.Ser798Pro | missense_variant | 0.14 |
embB | 4249699 | c.3186T>G | synonymous_variant | 0.15 |
aftB | 4268662 | p.Thr59Pro | missense_variant | 0.15 |
ethA | 4328025 | c.-552T>G | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |