Run ID: ERR4820305
Sample name:
Date: 01-04-2023 16:36:23
Number of reads: 291018
Percentage reads mapped: 99.41
Strain: lineage3
Drug-resistance: HR-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 |
---|---|---|---|---|---|
katG | 2155064 | p.Ala350Thr | missense_variant | 0.22 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9283 | p.Gly661Asp | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
gyrA | 9777 | p.Asn826Asp | missense_variant | 1.0 |
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 |
rpoB | 762636 | p.Lys944Glu | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764081 | p.Glu238Lys | missense_variant | 0.33 |
rpoC | 764181 | p.Asp271Gly | 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 |
Rv1258c | 1407083 | c.258G>T | synonymous_variant | 0.38 |
Rv1258c | 1407255 | p.Ala29Val | missense_variant | 0.11 |
rrs | 1471656 | n.-190G>A | upstream_gene_variant | 0.29 |
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 |
PPE35 | 2169239 | c.1374T>C | synonymous_variant | 0.22 |
PPE35 | 2170362 | p.Glu84Gly | missense_variant | 0.29 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
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 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 1.0 |
ahpC | 2725948 | c.-245C>A | upstream_gene_variant | 0.17 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747206 | c.393G>T | synonymous_variant | 0.29 |
ribD | 2986763 | c.-76G>A | upstream_gene_variant | 0.18 |
ribD | 2986992 | p.Gly52Ser | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3613100 | p.Ala6Val | missense_variant | 0.29 |
fbiB | 3642427 | p.Val298Ala | missense_variant | 0.17 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.33 |
clpC1 | 4039674 | p.Pro344Gln | missense_variant | 0.29 |
clpC1 | 4039676 | c.1029G>A | synonymous_variant | 0.29 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.29 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243484 | c.252C>T | synonymous_variant | 0.15 |
aftB | 4267146 | p.Ala564Val | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |