Run ID: ERR11049975
Sample name:
Date: 02-04-2023 05:39:16
Number of reads: 4061565
Percentage reads mapped: 99.62
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
gid | 4408100 | c.102delG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.2 |
fgd1 | 491315 | p.Gly178Ala | missense_variant | 0.16 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.25 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.24 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.2 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.3 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.36 |
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 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170037 | c.576C>G | synonymous_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.3 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.17 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.2 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.78 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.5 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>C | synonymous_variant | 0.25 |
whiB7 | 3568428 | c.252A>C | synonymous_variant | 0.22 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.17 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.67 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.6 |
embC | 4239930 | p.Gly23Glu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.61 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.26 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.24 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.35 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |