Run ID: ERR11050368
Sample name:
Date: 03-04-2023 00:58:04
Number of reads: 4408506
Percentage reads mapped: 99.65
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 |
---|---|---|---|---|
gyrB | 5783 | p.Thr182Ser | missense_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.19 |
mshA | 576106 | c.759C>G | synonymous_variant | 0.18 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.27 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.24 |
mmpL5 | 778585 | c.-105C>T | upstream_gene_variant | 1.0 |
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 | 0.99 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.27 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.36 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.25 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>C | synonymous_variant | 0.22 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.38 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.35 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.29 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.5 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.78 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embC | 4240061 | p.Phe67Val | missense_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.26 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.39 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.22 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.24 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |