Run ID: ERR4797042
Sample name:
Date: 01-04-2023 07:19:12
Number of reads: 4487844
Percentage reads mapped: 99.64
Strain: lineage3.1.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.25 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.16 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.36 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.38 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781676 | c.117C>T | synonymous_variant | 1.0 |
Rv1258c | 1406242 | p.Ala367Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471793 | n.-53G>T | upstream_gene_variant | 0.31 |
rrs | 1471805 | n.-41C>A | upstream_gene_variant | 0.45 |
rrs | 1471812 | n.-34C>A | upstream_gene_variant | 0.2 |
rrs | 1472650 | n.805A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473400 | n.-258C>T | upstream_gene_variant | 0.25 |
rrl | 1474479 | n.822A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476068 | n.2411C>A | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1674079 | p.Pro214Ala | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918104 | c.165G>A | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.16 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.15 |
fbiD | 3339044 | c.-74T>G | upstream_gene_variant | 0.19 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.8 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474208 | p.Glu68* | stop_gained | 0.23 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243700 | c.468C>A | synonymous_variant | 0.25 |
embB | 4247033 | p.Ser174Cys | missense_variant | 0.21 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.33 |
ethA | 4326041 | p.Leu478Arg | missense_variant | 1.0 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.28 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |