Variant #0000167075 (NC_000001.10:g.171080089A>G, NM_001002294.2:c.778A>G (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.171080089A>G
DNA change (hg38) g.171110948A>G
Published as -
ISCN -
DB-ID FMO3_000031 See all 3 reported entries
Variant remarks expected to affect N-oxygenation and S-oxygenation of drug substrates of FMO3
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-03-02 14:30:48 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 6 c.778A>G - r.(?) p.(Met260Val)


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