Run ID: ERR4818792
Sample name:
Date: 01-04-2023 15:45:09
Number of reads: 253262
Percentage reads mapped: 99.62
Strain: lineage3
Drug-resistance: Other
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
fgd1 | 490688 | c.-95G>T | upstream_gene_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620340 | c.450C>T | synonymous_variant | 0.2 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.25 |
rpoB | 762194 | c.2388G>A | synonymous_variant | 0.22 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.75 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777020 | c.1461G>A | synonymous_variant | 0.22 |
mmpL5 | 777891 | p.Gln197Arg | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833522 | c.-20G>A | upstream_gene_variant | 0.14 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.22 |
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 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2222450 | p.Ala239Thr | missense_variant | 0.29 |
Rv1979c | 2222645 | p.Leu174Ile | missense_variant | 0.22 |
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 |
kasA | 2518383 | p.Leu90Pro | missense_variant | 0.67 |
eis | 2714700 | c.633C>T | synonymous_variant | 0.29 |
ahpC | 2725973 | c.-220A>G | upstream_gene_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339690 | c.573C>G | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640383 | c.-160A>G | upstream_gene_variant | 0.25 |
fbiA | 3640431 | c.-112T>A | upstream_gene_variant | 0.25 |
clpC1 | 4039303 | p.Trp468Arg | missense_variant | 0.4 |
clpC1 | 4039572 | p.Ala378Val | missense_variant | 0.4 |
clpC1 | 4040182 | p.Gly175Cys | missense_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246555 | c.42G>T | synonymous_variant | 0.18 |
embB | 4247230 | c.717G>A | synonymous_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407594 | c.609G>A | synonymous_variant | 0.18 |