Run ID: ERR4812734
Sample name:
Date: 01-04-2023 12:17:37
Number of reads: 239733
Percentage reads mapped: 98.7
Strain:
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | 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 |
ethA | 4327380 | p.Tyr32Asp | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7597 | p.Met99Lys | missense_variant | 0.2 |
gyrA | 8101 | p.Thr267Ile | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764820 | p.Trp484Ser | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777350 | c.1131G>T | synonymous_variant | 0.2 |
mmpL5 | 779364 | c.-884C>A | upstream_gene_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475029 | n.1377delG | non_coding_transcript_exon_variant | 0.4 |
inhA | 1673541 | c.-661G>T | upstream_gene_variant | 0.5 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101891 | c.1152C>A | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726651 | c.459G>T | synonymous_variant | 0.17 |
Rv2752c | 3065903 | c.288_289insT | frameshift_variant | 1.0 |
thyA | 3073897 | c.574delG | frameshift_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448657 | p.Gly52* | stop_gained | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641331 | c.793dupG | frameshift_variant | 0.17 |
rpoA | 3877566 | c.942C>T | synonymous_variant | 0.12 |
clpC1 | 4040611 | p.His32Asn | missense_variant | 0.4 |
clpC1 | 4040627 | p.Asn26Lys | missense_variant | 0.4 |
embC | 4242558 | p.Gln899Arg | missense_variant | 0.67 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407858 | c.345G>T | synonymous_variant | 0.67 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |