Run ID: ERR2229479
Sample name:
Date: 31-03-2023 17:14:41
Number of reads: 1079602
Percentage reads mapped: 99.42
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 | 575186 | c.-161delG | upstream_gene_variant | 0.11 |
mshA | 575382 | p.Leu12* | stop_gained | 0.17 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.24 |
rpoB | 762652 | p.Trp949Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775817 | c.2664T>C | synonymous_variant | 0.12 |
mmpL5 | 775820 | c.2661G>A | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416786 | c.561delC | frameshift_variant | 0.2 |
embR | 1417177 | c.171C>T | synonymous_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 | 1474438 | n.781A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
inhA | 1674081 | c.-121C>T | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168043 | p.Ala857Gly | missense_variant | 0.11 |
PPE35 | 2168051 | c.2562G>C | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.36 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.12 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.19 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.19 |
kasA | 2519201 | p.Arg363Ser | missense_variant | 0.13 |
kasA | 2519356 | c.1242G>A | synonymous_variant | 0.13 |
kasA | 2519359 | c.1245T>G | synonymous_variant | 0.13 |
pepQ | 2859576 | c.843C>T | synonymous_variant | 0.17 |
Rv2752c | 3065809 | p.Val128Ala | missense_variant | 0.1 |
Rv2752c | 3065934 | p.His86Gln | missense_variant | 0.13 |
thyX | 3067549 | p.Thr133Pro | missense_variant | 0.25 |
thyX | 3067602 | p.Arg115Leu | missense_variant | 0.15 |
Rv3236c | 3612822 | p.Leu99Val | missense_variant | 0.13 |
fbiB | 3641728 | p.Glu65Gly | missense_variant | 1.0 |
fbiB | 3641827 | p.Arg98Leu | missense_variant | 0.12 |
rpoA | 3878182 | p.Asp109Gly | missense_variant | 0.13 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.21 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.21 |
embC | 4241697 | p.Ala612Glu | missense_variant | 0.14 |
embC | 4242350 | p.Pro830Thr | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.3 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.25 |
embB | 4247017 | c.504G>T | synonymous_variant | 0.17 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |