Run ID: SRR18714994
Sample name:
Date: 03-04-2023 20:14:25
Number of reads: 4977291
Percentage reads mapped: 99.68
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 | 9647 | c.2346C>G | synonymous_variant | 0.24 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.21 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.27 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.28 |
rpsL | 781395 | c.-165T>C | upstream_gene_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 | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673162 | c.-278T>C | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.3 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.2 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.21 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.57 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.21 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.19 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.21 |
Rv3236c | 3612047 | p.Ala357Val | missense_variant | 1.0 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.33 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.5 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.73 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244662 | p.Ala477Gly | missense_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.42 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.12 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.13 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.13 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.24 |
embB | 4246820 | p.Pro103Thr | missense_variant | 1.0 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.41 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.31 |
ethA | 4326505 | c.969C>G | 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 |