Run ID: ERR2515522
Sample name:
Date: 31-03-2023 20:58:46
Number of reads: 475896
Percentage reads mapped: 99.69
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
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 |
mmpL5 | 776773 | p.His570Asn | missense_variant | 0.11 |
mmpR5 | 779303 | p.Arg105Pro | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303246 | p.Thr106Ala | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476785 | n.3128A>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673702 | c.266_268delCCG | disruptive_inframe_deletion | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103061 | c.-19C>A | upstream_gene_variant | 0.13 |
katG | 2154150 | c.1962C>A | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168961 | p.Gly551Val | missense_variant | 0.11 |
PPE35 | 2170246 | p.Ser123Pro | missense_variant | 0.11 |
PPE35 | 2170461 | p.Gly51Glu | missense_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 | 2715526 | c.-194C>T | upstream_gene_variant | 0.11 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747322 | p.Thr93Ala | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640928 | p.Thr129Ile | missense_variant | 0.11 |
fbiB | 3641584 | p.Val17Ala | missense_variant | 0.1 |
rpoA | 3878357 | p.Val51Ile | missense_variant | 0.14 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4240765 | c.903C>T | synonymous_variant | 0.12 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244691 | p.Tyr487His | missense_variant | 0.11 |
embA | 4246075 | p.Leu948Arg | missense_variant | 0.15 |
embB | 4249378 | c.2865G>T | synonymous_variant | 0.13 |
aftB | 4267744 | p.Arg365Trp | missense_variant | 0.14 |
aftB | 4267830 | p.Gly336Asp | missense_variant | 0.17 |
ubiA | 4269862 | c.-29G>A | upstream_gene_variant | 0.13 |
ubiA | 4269997 | c.-164C>G | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |