Run ID: ERR2228886
Sample name:
Date: 31-03-2023 16:24:56
Number of reads: 1414463
Percentage reads mapped: 99.57
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 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.15 |
rpoB | 762543 | p.Thr913Ser | missense_variant | 0.13 |
rpoB | 763149 | p.Phe1115Leu | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.35 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.35 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.28 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.28 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673934 | c.-268C>T | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.29 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.21 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.21 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168876 | p.Phe579Leu | missense_variant | 0.15 |
PPE35 | 2169056 | c.1557A>T | synonymous_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.18 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.12 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.11 |
Rv2752c | 3065364 | c.828G>T | synonymous_variant | 0.18 |
ald | 3086727 | c.-93G>A | upstream_gene_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.64 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.14 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244825 | c.1593G>T | synonymous_variant | 0.12 |
aftB | 4267975 | p.Ser288Ala | missense_variant | 0.22 |
ethA | 4328025 | c.-552T>G | upstream_gene_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |