Run ID: ERR2228825
Sample name:
Date: 31-03-2023 16:22:15
Number of reads: 967398
Percentage reads mapped: 99.26
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 |
---|---|---|---|---|
gyrB | 6435 | p.Asn399Ser | missense_variant | 0.13 |
gyrA | 7300 | c.-2A>T | upstream_gene_variant | 0.31 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8762 | c.1461G>T | synonymous_variant | 0.25 |
mshA | 576440 | p.Cys365Gly | missense_variant | 0.21 |
rpoB | 759724 | c.-83A>T | upstream_gene_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.95 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304963 | p.Trp678Ser | missense_variant | 0.15 |
embR | 1416518 | p.Leu277Arg | missense_variant | 0.32 |
embR | 1417371 | c.-24A>G | upstream_gene_variant | 0.14 |
atpE | 1460898 | c.-147T>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471910 | n.65T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473769 | n.112T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476161 | n.2504A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476162 | n.2505A>T | non_coding_transcript_exon_variant | 0.22 |
rpsA | 1834794 | p.Tyr418Ser | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918514 | p.Val192Gly | missense_variant | 0.22 |
katG | 2155722 | c.390G>A | synonymous_variant | 0.17 |
PPE35 | 2168460 | p.Asn718Ile | missense_variant | 0.38 |
PPE35 | 2168680 | c.1932delT | frameshift_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168738 | c.1875T>C | synonymous_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.22 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.17 |
Rv1979c | 2223141 | c.24A>T | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518610 | p.Thr166Pro | missense_variant | 0.33 |
ahpC | 2726462 | p.Glu90Asp | missense_variant | 0.25 |
pepQ | 2859517 | p.Gln301Arg | missense_variant | 0.12 |
Rv2752c | 3064789 | p.Leu468Ser | missense_variant | 0.11 |
Rv2752c | 3065954 | p.Thr80Pro | missense_variant | 0.18 |
thyX | 3067839 | p.Val36Ala | missense_variant | 0.12 |
thyA | 3073804 | p.Glu223Ala | missense_variant | 0.31 |
thyA | 3074270 | p.Asn68Asp | missense_variant | 0.33 |
thyA | 3074281 | p.Arg64Leu | missense_variant | 0.29 |
Rv3236c | 3612506 | p.His204Leu | missense_variant | 0.25 |
Rv3236c | 3612939 | p.Thr60Ser | missense_variant | 0.5 |
fbiB | 3641953 | p.Leu140Arg | missense_variant | 0.31 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243944 | p.Thr238Pro | missense_variant | 0.26 |
embB | 4246736 | p.Thr75Pro | missense_variant | 0.26 |
embB | 4249653 | p.His1047Pro | missense_variant | 0.2 |
embB | 4249794 | p.Ile1094Thr | missense_variant | 0.15 |
aftB | 4267029 | p.Asp603Val | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-3_*1408del | transcript_ablation | 1.0 |