Run ID: ERR4812866
Sample name:
Date: 01-04-2023 12:23:23
Number of reads: 274372
Percentage reads mapped: 99.39
Strain: lineage4
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247469 | p.Tyr319Ser | missense_variant | 1.0 | ethambutol |
gid | 4407952 | p.Pro84Leu | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6928 | c.-374G>A | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
rpoB | 759923 | c.117C>T | synonymous_variant | 0.11 |
rpoB | 760327 | p.Val174Ala | missense_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778894 | c.-414T>C | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303679 | p.Arg250Gln | missense_variant | 0.33 |
Rv1258c | 1406521 | p.Gly274Arg | missense_variant | 0.18 |
atpE | 1461138 | p.Gly32Ser | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473005 | n.1160C>A | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833371 | c.-171G>A | upstream_gene_variant | 0.5 |
rpsA | 1834339 | p.Asp266Glu | missense_variant | 0.15 |
rpsA | 1834985 | c.1445dupG | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
ndh | 2102050 | c.993T>G | synonymous_variant | 0.5 |
katG | 2155213 | p.Trp300Leu | missense_variant | 0.18 |
PPE35 | 2168998 | p.Ile539Val | missense_variant | 0.88 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518412 | p.Ser100Gly | missense_variant | 0.15 |
folC | 2746749 | p.Gly284Trp | missense_variant | 1.0 |
pepQ | 2859369 | c.1050A>G | synonymous_variant | 0.22 |
thyX | 3068146 | c.-201T>C | upstream_gene_variant | 0.2 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473957 | c.-50C>T | upstream_gene_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568558 | p.Thr41Ile | missense_variant | 0.29 |
whiB7 | 3568720 | c.-41C>T | upstream_gene_variant | 0.11 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.29 |
alr | 3841468 | c.-48C>T | upstream_gene_variant | 0.14 |
ddn | 3987275 | c.432C>T | synonymous_variant | 0.15 |
embC | 4241921 | p.Gly687Trp | missense_variant | 0.25 |
ethA | 4327267 | p.Trp69Cys | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408388 | c.-186C>A | upstream_gene_variant | 0.5 |