Variant #0000167122 (NC_000001.10:g.171086481C>T, NM_001002294.2:c.1498C>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.171086481C>T
DNA change (hg38) g.171117341C>T
Published as -
ISCN -
DB-ID FMO3_000016 See all 9 reported entries
Variant remarks cDNA expression cloning in E.coli shows no N-oxygenation activity
Reference PubMed: Yamazaki 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Ornicha Prapapan
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-02-26 15:04:46 +01:00 (CET)
Date last edited 2020-06-05 15:15:50 +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 +/+ 9 c.1498C>T - r.(?) p.Arg500*


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