Run ID: ERR4831956
Sample name:
Date: 01-04-2023 21:13:52
Number of reads: 945314
Percentage reads mapped: 99.41
Strain: lineage2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.1 | East-Asian (non-Beijing) | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 0.96 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289123 | c.118delG | frameshift_variant | 1.0 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Ala | missense_variant | 0.64 | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.15 |
rpoB | 762109 | p.Pro768Gln | missense_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777663 | p.Ala273Gly | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303868 | p.Asp313Gly | missense_variant | 1.0 |
fbiC | 1304443 | p.Ala505Thr | missense_variant | 1.0 |
Rv1258c | 1407473 | c.-133C>A | upstream_gene_variant | 0.15 |
embR | 1417185 | p.Leu55Ile | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473874 | n.217G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474076 | n.419C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.15 |
inhA | 1674585 | c.384T>G | synonymous_variant | 1.0 |
rpsA | 1833399 | c.-143G>T | upstream_gene_variant | 0.17 |
rpsA | 1833498 | c.-44A>G | upstream_gene_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156019 | p.Glu31Asp | missense_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222902 | p.Arg88Leu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290237 | c.-996G>T | upstream_gene_variant | 0.17 |
kasA | 2518725 | p.Ala204Glu | missense_variant | 0.13 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.18 |
pepQ | 2859887 | p.Ala178Ser | missense_variant | 0.12 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.1 |
thyX | 3067283 | c.663C>A | synonymous_variant | 0.15 |
thyX | 3067586 | c.360C>A | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612471 | p.Glu216* | stop_gained | 0.14 |
clpC1 | 4038693 | p.Ser671Tyr | missense_variant | 0.15 |
clpC1 | 4039047 | p.Gly553Val | missense_variant | 0.18 |
embC | 4241549 | p.Gly563Arg | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244909 | c.1677C>T | synonymous_variant | 0.12 |
embB | 4246088 | c.-426A>G | upstream_gene_variant | 1.0 |
embB | 4249424 | c.2912delT | frameshift_variant | 0.1 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268684 | p.Gln51His | missense_variant | 0.13 |
ubiA | 4269742 | p.Leu31Pro | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |