Run ID: ERR2229652
Sample name:
Date: 31-03-2023 17:23:33
Number of reads: 261226
Percentage reads mapped: 99.23
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 |
gyrA | 8953 | p.Gln551Leu | missense_variant | 0.18 |
mshA | 575711 | p.Lys122* | stop_gained | 0.5 |
mshA | 576565 | c.1218G>A | synonymous_variant | 0.33 |
rpoB | 761082 | p.Gly426Cys | missense_variant | 0.22 |
rpoB | 762972 | p.Gln1056Lys | missense_variant | 0.12 |
rpoC | 764094 | p.Arg242His | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779613 | c.-708C>A | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801100 | p.Gly98Trp | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472493 | n.648T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474324 | n.667C>A | non_coding_transcript_exon_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918695 | c.756G>T | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169596 | p.Phe339Trp | missense_variant | 0.25 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.44 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.25 |
PPE35 | 2170331 | c.282G>A | synonymous_variant | 0.15 |
Rv1979c | 2223153 | c.12G>T | synonymous_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714708 | p.Gly209Cys | missense_variant | 0.67 |
ahpC | 2726376 | p.Pro62Thr | missense_variant | 0.29 |
ahpC | 2726487 | p.Gln99Lys | missense_variant | 0.5 |
ahpC | 2726592 | p.Val134Met | missense_variant | 0.4 |
pepQ | 2859379 | p.Gly347Val | missense_variant | 0.25 |
ribD | 2986944 | p.Asp36Tyr | missense_variant | 0.4 |
ribD | 2987572 | p.Thr245Ile | missense_variant | 0.33 |
Rv2752c | 3065220 | c.972C>A | synonymous_variant | 0.4 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.31 |
ddn | 3986844 | c.1A>T | initiator_codon_variant | 0.17 |
clpC1 | 4039944 | p.Ser254* | stop_gained | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.67 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.67 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.67 |
embB | 4249553 | p.Ile1014Phe | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |