Run ID: SRR14088379
Sample name:
Date: 03-04-2023 09:46:20
Number of reads: 2145135
Percentage reads mapped: 99.72
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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288868 | p.Val125Gly | missense_variant | 1.0 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
gid | 4408100 | c.102delG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7581 | p.Asp94Cys | missense_variant | 0.21 |
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 | 759620 | c.-187A>C | upstream_gene_variant | 0.26 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759988 | p.Ser61* | stop_gained | 0.25 |
rpoB | 759991 | p.Pro62Gln | missense_variant | 0.29 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763381 | c.12C>A | synonymous_variant | 0.13 |
rpoC | 763397 | p.Leu10Phe | missense_variant | 0.13 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
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 |
atpE | 1461187 | p.Arg48Leu | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471889 | n.44G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472782 | n.937G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474311 | n.654G>T | non_coding_transcript_exon_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168442 | p.Trp724Leu | missense_variant | 0.25 |
Rv1979c | 2222156 | p.Pro337Thr | missense_variant | 0.13 |
Rv1979c | 2222535 | c.630C>A | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223303 | c.-139G>T | upstream_gene_variant | 0.12 |
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 |
ald | 3086703 | c.-117T>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568857 | c.-178C>T | upstream_gene_variant | 1.0 |
rpoA | 3878646 | c.-139G>T | upstream_gene_variant | 0.17 |
clpC1 | 4039473 | p.Arg411Leu | missense_variant | 0.19 |
panD | 4044023 | c.259C>T | synonymous_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326341 | p.Pro378His | missense_variant | 0.19 |
ethA | 4326389 | p.Asp362Val | missense_variant | 0.15 |
ethA | 4326967 | p.Glu169Asp | missense_variant | 0.15 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
whiB6 | 4337780 | c.-383_*390del | transcript_ablation | 1.0 |