Run ID: ERR4815242
Sample name:
Date: 01-04-2023 13:45:10
Number of reads: 391761
Percentage reads mapped: 99.1
Strain: lineage3
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5628 | p.Ala130Glu | missense_variant | 0.11 |
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 | 491027 | p.Asn82Thr | missense_variant | 0.45 |
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 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778172 | c.-818G>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304265 | c.1335C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102959 | p.Asn28Lys | missense_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169406 | p.Asn403Asp | missense_variant | 0.14 |
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 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474162 | c.156G>A | synonymous_variant | 0.17 |
fbiB | 3642005 | c.471C>G | synonymous_variant | 1.0 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.36 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.12 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.12 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.11 |
clpC1 | 4039284 | p.Asp474Gly | missense_variant | 0.17 |
clpC1 | 4040232 | p.Arg158Leu | missense_variant | 0.22 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.93 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267601 | c.1236C>T | synonymous_variant | 0.14 |
aftB | 4269321 | c.-485G>A | upstream_gene_variant | 0.17 |
ethA | 4326912 | p.Val188Ile | missense_variant | 1.0 |
whiB6 | 4338256 | p.Ala89Val | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |