Run ID: SRR6046076
Sample name:
Date: 04-04-2023 12:10:40
Number of reads: 821495
Percentage reads mapped: 99.37
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 | Drugs |
---|---|---|---|---|---|
ethA | 4327411 | p.Trp21* | stop_gained | 0.11 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8337 | p.Leu346Val | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576053 | p.Asp236Tyr | missense_variant | 0.2 |
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 |
rpoC | 764017 | c.648G>A | synonymous_variant | 0.11 |
rpoC | 767166 | p.Arg1266Leu | missense_variant | 0.17 |
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 |
fbiC | 1303683 | c.753G>A | synonymous_variant | 0.17 |
Rv1258c | 1406620 | p.Pro241Ser | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473471 | n.-187C>T | upstream_gene_variant | 0.12 |
inhA | 1673541 | c.-661G>T | upstream_gene_variant | 0.11 |
rpsA | 1834921 | c.1380G>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155324 | p.Ala263Glu | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168991 | p.Ala541Asp | missense_variant | 0.13 |
PPE35 | 2170540 | c.73C>T | synonymous_variant | 0.11 |
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 | 2518818 | p.Asp235Gly | missense_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747725 | c.-127C>A | upstream_gene_variant | 0.11 |
pepQ | 2860251 | c.168C>T | synonymous_variant | 0.14 |
thyX | 3067526 | c.420C>G | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339254 | p.Thr46Met | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474358 | p.Asp118Asn | missense_variant | 0.12 |
fprA | 3474797 | p.His264Arg | missense_variant | 0.11 |
alr | 3840891 | p.Thr177Asn | missense_variant | 0.11 |
alr | 3840894 | p.Leu176Pro | missense_variant | 0.11 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
embC | 4240088 | p.Gly76Ser | missense_variant | 0.12 |
embC | 4240479 | p.Gly206Glu | missense_variant | 0.11 |
embC | 4240627 | p.Asp255Glu | missense_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242959 | p.Leu1033Met | missense_variant | 0.17 |
embA | 4246072 | p.Asn947Ile | missense_variant | 0.11 |
aftB | 4268794 | p.Val15Met | missense_variant | 0.11 |
ethR | 4327709 | p.Ala54Val | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |