Run ID: ERR4797612
Sample name:
Date: 01-04-2023 07:46:42
Number of reads: 2734452
Percentage reads mapped: 99.61
Strain: lineage3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472751 | n.906A>G | non_coding_transcript_exon_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289200 | p.Cys14* | stop_gained | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
gid | 4407851 | c.351delG | frameshift_variant | 1.0 | streptomycin |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
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 | 766488 | p.Pro1040Arg | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777266 | c.1215G>C | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303255 | p.Thr109Ala | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472270 | n.425T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474059 | n.402C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474145 | n.488T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474260 | n.603A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474910 | n.1254delG | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475923 | n.2269delA | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674402 | c.201C>T | synonymous_variant | 0.12 |
rpsA | 1833411 | c.-131G>C | upstream_gene_variant | 0.13 |
rpsA | 1833446 | c.-96T>C | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102019 | p.Tyr342Asp | missense_variant | 1.0 |
ndh | 2102932 | c.111C>T | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168488 | p.Ile709Phe | missense_variant | 0.25 |
PPE35 | 2170330 | p.Ala95Thr | missense_variant | 0.11 |
PPE35 | 2170420 | p.Met65Val | missense_variant | 0.1 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
thyX | 3067254 | p.Glu231Gly | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339547 | p.Leu144Ile | missense_variant | 0.11 |
fprA | 3473820 | c.-187C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3640692 | c.-843C>T | upstream_gene_variant | 0.12 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.15 |
embC | 4241097 | p.Ser412Leu | missense_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244807 | c.1575G>T | synonymous_variant | 0.1 |
embB | 4248568 | p.Trp685Cys | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |