Run ID: SRR6650350
Sample name:
Date: 15-08-2023 07:36:30
Number of reads: 814917
Percentage reads mapped: 99.55
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | R | pncA p.Thr177Pro (0.19) |
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288713 | p.Thr177Pro | missense_variant | 0.19 | pyrazinamide |
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 | 491008 | p.Thr76Pro | missense_variant | 0.2 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.22 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576489 | p.Val381Gly | missense_variant | 0.2 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.33 |
ccsA | 619844 | c.-47T>G | upstream_gene_variant | 0.19 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.26 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.17 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.32 |
ccsA | 620773 | p.Ile295Val | missense_variant | 0.24 |
rpoB | 759611 | c.-196G>C | upstream_gene_variant | 0.22 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.56 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.56 |
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 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.25 |
mmpR5 | 779363 | p.Leu125Arg | missense_variant | 0.36 |
mmpR5 | 779369 | p.Asp127Ala | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781524 | c.-36C>A | upstream_gene_variant | 0.29 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471710 | n.-136T>G | upstream_gene_variant | 0.25 |
rrl | 1473948 | n.291C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.6 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918394 | p.Val152Gly | missense_variant | 0.25 |
ndh | 2102509 | c.534T>G | synonymous_variant | 0.18 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.46 |
ndh | 2103235 | c.-193C>G | upstream_gene_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>G | synonymous_variant | 0.25 |
PPE35 | 2169308 | c.1305C>G | synonymous_variant | 0.25 |
PPE35 | 2169314 | p.Asn433Lys | missense_variant | 0.2 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.2 |
PPE35 | 2170072 | p.Gly181Arg | missense_variant | 0.14 |
PPE35 | 2170425 | p.Val63Gly | missense_variant | 0.2 |
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 | 2518147 | c.33C>T | synonymous_variant | 0.26 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.22 |
kasA | 2518605 | p.Val164Gly | missense_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.25 |
ahpC | 2726286 | p.Gly32Arg | missense_variant | 0.27 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.21 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.3 |
Rv3083 | 3449089 | p.Met196Val | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642751 | p.Asp406Ala | missense_variant | 0.22 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.2 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
ddn | 3986929 | p.Tyr29Ser | missense_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.22 |
embA | 4242406 | c.-827A>C | upstream_gene_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244350 | p.Leu373Pro | missense_variant | 1.0 |
embB | 4247125 | c.612G>C | synonymous_variant | 0.13 |
embB | 4247173 | c.660G>T | synonymous_variant | 0.13 |
embB | 4247623 | c.1110G>C | synonymous_variant | 0.38 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.33 |
aftB | 4267843 | p.Asp332Asn | missense_variant | 0.15 |
aftB | 4268758 | p.Ile27Val | missense_variant | 0.17 |
aftB | 4268776 | p.Ser21Gly | missense_variant | 0.23 |
ubiA | 4269460 | p.Ala125Gly | missense_variant | 0.22 |
ubiA | 4269479 | p.Met119Val | missense_variant | 0.33 |
aftB | 4269486 | c.-650T>G | upstream_gene_variant | 0.5 |
aftB | 4269504 | c.-668A>G | upstream_gene_variant | 0.4 |
ubiA | 4269511 | p.Val108Gly | missense_variant | 0.33 |
ubiA | 4269856 | c.-23G>A | upstream_gene_variant | 0.25 |
ethA | 4326903 | p.Val191Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |