Run ID: SRR14088350
Sample name:
Date: 03-04-2023 09:45:13
Number of reads: 840518
Percentage reads mapped: 99.45
Strain: lineage3
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8837 | c.1536C>A | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491502 | p.Glu240Asp | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576540 | p.Trp398Leu | missense_variant | 0.13 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761711 | c.1905C>T | synonymous_variant | 0.12 |
rpoB | 762274 | p.Ala823Val | missense_variant | 0.15 |
rpoB | 762310 | p.His835Arg | missense_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763468 | c.99G>T | synonymous_variant | 0.13 |
rpoC | 765688 | c.2319G>T | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.16 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.15 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.15 |
mmpS5 | 778626 | c.279_280insGTGAGCG | frameshift_variant | 0.14 |
mmpS5 | 778630 | p.Leu92Phe | missense_variant | 0.13 |
mmpS5 | 778632 | c.267_273delGCTCACC | frameshift_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781763 | c.204C>A | synonymous_variant | 0.12 |
fbiC | 1304202 | c.1272G>A | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473615 | n.-43G>T | upstream_gene_variant | 0.14 |
rrl | 1473780 | n.123G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475373 | n.1716G>C | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673495 | p.Leu19Pro | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101762 | c.1281C>A | synonymous_variant | 0.12 |
ndh | 2102565 | p.Arg160Trp | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156361 | c.-250G>T | upstream_gene_variant | 0.12 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.21 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.17 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.17 |
PPE35 | 2169713 | c.900C>G | synonymous_variant | 0.19 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.29 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.55 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.6 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.14 |
PPE35 | 2170415 | c.198A>G | synonymous_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 |
pncA | 2290203 | c.-962C>T | upstream_gene_variant | 0.14 |
kasA | 2518407 | p.Ala98Val | missense_variant | 0.14 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.12 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.33 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.29 |
eis | 2715481 | c.-149G>T | upstream_gene_variant | 0.2 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726269 | p.Val26Gly | missense_variant | 0.24 |
folC | 2746678 | c.921T>C | synonymous_variant | 0.14 |
folC | 2747630 | c.-32G>A | upstream_gene_variant | 0.22 |
pepQ | 2859548 | p.Gly291Ser | missense_variant | 0.12 |
pepQ | 2859737 | p.Gly228Trp | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449049 | c.546C>G | synonymous_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474259 | p.Gly85Ser | missense_variant | 0.14 |
Rv3236c | 3612016 | c.1101G>A | synonymous_variant | 0.18 |
Rv3236c | 3612708 | c.409T>C | synonymous_variant | 0.17 |
Rv3236c | 3612838 | c.279G>A | synonymous_variant | 0.12 |
Rv3236c | 3612848 | p.Leu90Pro | missense_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.21 |
ddn | 3986760 | c.-84G>T | upstream_gene_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.17 |
clpC1 | 4040063 | c.642G>T | synonymous_variant | 0.14 |
panD | 4043909 | p.Pro125Thr | missense_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242658 | c.-575A>T | upstream_gene_variant | 0.13 |
embA | 4244970 | p.Leu580Met | missense_variant | 0.22 |
embA | 4245700 | p.Gly823Glu | missense_variant | 0.18 |
embB | 4246133 | c.-381G>A | upstream_gene_variant | 0.15 |
embB | 4247473 | c.960C>T | synonymous_variant | 0.11 |
embB | 4249069 | c.2556A>G | synonymous_variant | 0.11 |
embB | 4249258 | c.2745G>T | synonymous_variant | 1.0 |
aftB | 4267583 | c.1254C>T | synonymous_variant | 0.2 |
aftB | 4267760 | p.Asp359Glu | missense_variant | 0.22 |
whiB6 | 4338286 | c.235delG | frameshift_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408070 | p.Trp45Arg | missense_variant | 1.0 |