Variant #0000167025 (NC_000001.10:g.171076952C>T, NM_001002294.2:c.458C>T (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.171076952C>T
DNA change (hg38) g.171107811C>T
Published as -
ISCN -
DB-ID FMO3_000001 See all 6 reported entries
Variant remarks variant expected to influence metabolism of drug (xenobiotic) substrates of FMO3 that undergo N- or S-oxygenation; impaired benzydamine N-oxygenation in compound het with E305X or with S173R
Reference PubMed: Mayatepek 2004
ClinVar ID -
dbSNP ID rs72549326
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00102 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-02-11 19:15:22 +01:00 (CET)
Date last edited 2020-06-05 15:14:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 4 c.458C>T - r.(?) p.Pro153Leu


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