Run ID: ERR2229750
Sample name:
Date: 31-03-2023 17:35:10
Number of reads: 1129117
Percentage reads mapped: 99.25
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491308 | c.534_541delCCCGGCGG | frameshift_variant | 0.17 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
rpoB | 759742 | c.-65G>A | upstream_gene_variant | 0.25 |
rpoC | 765226 | p.Ile619Met | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775974 | p.Leu836Trp | missense_variant | 0.11 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.2 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.2 |
mmpL5 | 776729 | c.1752C>T | synonymous_variant | 0.2 |
mmpL5 | 778963 | c.-483G>T | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417156 | c.192A>C | synonymous_variant | 0.13 |
embR | 1417172 | c.175dupC | frameshift_variant | 0.14 |
embR | 1417540 | c.-193C>G | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473913 | n.258delA | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474030 | n.373G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474076 | n.419C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476023 | n.2366C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476140 | n.2485delA | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.32 |
inhA | 1674199 | c.-3C>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155326 | c.786A>T | synonymous_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169606 | p.Asn336Thr | missense_variant | 0.1 |
PPE35 | 2169618 | p.Phe332Gly | missense_variant | 0.1 |
PPE35 | 2169623 | c.990T>C | synonymous_variant | 0.22 |
PPE35 | 2169629 | c.984T>C | synonymous_variant | 0.13 |
PPE35 | 2169671 | c.942C>G | synonymous_variant | 0.14 |
PPE35 | 2169674 | c.939T>C | synonymous_variant | 0.13 |
PPE35 | 2169680 | c.933A>G | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.65 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.65 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.12 |
eis | 2714767 | p.Gly189Val | missense_variant | 0.14 |
eis | 2714953 | p.Gly127Val | missense_variant | 0.13 |
ahpC | 2726523 | p.Leu111Ile | missense_variant | 0.14 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.19 |
Rv3236c | 3612460 | c.657G>A | synonymous_variant | 0.13 |
fbiA | 3640531 | c.-12C>T | upstream_gene_variant | 0.17 |
rpoA | 3877991 | p.Lys173Glu | missense_variant | 0.1 |
embC | 4241143 | c.1281C>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244610 | p.Ala460Pro | missense_variant | 0.11 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.35 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.56 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.56 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.46 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.43 |
aftB | 4268086 | p.Ser251Pro | missense_variant | 0.15 |
ethR | 4327781 | p.Arg78Leu | missense_variant | 0.12 |
ethA | 4328465 | c.-992C>A | upstream_gene_variant | 0.14 |
whiB6 | 4338261 | c.261G>C | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |