Run ID: ERR2229053
Sample name:
Date: 31-03-2023 16:33:55
Number of reads: 1403990
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 | 575305 | c.-43C>A | upstream_gene_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.26 |
ccsA | 620172 | p.Cys94Trp | missense_variant | 0.1 |
ccsA | 620262 | c.372C>T | synonymous_variant | 0.14 |
ccsA | 620406 | c.516G>T | synonymous_variant | 0.12 |
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 | 1474619 | n.962G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475843 | n.2186G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.22 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.23 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.21 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.21 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.21 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
fabG1 | 1674136 | p.Ser233Pro | missense_variant | 0.14 |
tlyA | 1917846 | c.-94C>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 0.97 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.47 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.14 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.13 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.24 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.24 |
whiB7 | 3568418 | c.250_261delGGACGTCCGCGC | conservative_inframe_deletion | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.2 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.23 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.18 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.18 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.15 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.12 |
aftB | 4267889 | c.948C>A | synonymous_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |