Run ID: SRR6964552
Sample name:
Date: 04-04-2023 18:16:50
Number of reads: 3852091
Percentage reads mapped: 99.33
Strain: lineage3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.36 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.1 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.17 | isoniazid |
gid | 4408025 | p.Glu60* | stop_gained | 0.47 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.18 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.19 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8948 | c.1647G>A | synonymous_variant | 0.61 |
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 | 0.87 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.44 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.91 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.12 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777323 | c.1158C>T | synonymous_variant | 0.11 |
mmpL5 | 777647 | c.834C>T | synonymous_variant | 0.49 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
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 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.54 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.91 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.96 |
pepQ | 2859841 | p.Ile193Thr | missense_variant | 0.42 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474901 | p.Ser299Arg | missense_variant | 0.52 |
fprA | 3474993 | c.987G>A | synonymous_variant | 0.5 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.17 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 0.29 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.11 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.85 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.12 |
embB | 4249000 | c.2487T>G | synonymous_variant | 0.61 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.15 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |