Variant #0000167077 (NC_000001.10:g.171086305T>C, NM_001002294.2:c.1322T>C (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.171086305T>C
DNA change (hg38) g.171117165T>C
Published as -
ISCN -
DB-ID FMO3_000081 See all 2 reported entries
Variant remarks Expected to affect N-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) 6.0E-5 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-02-28 23:22:22 +01:00 (CET)
Date last edited 2017-04-05 15:31:15 +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.1322T>C - r.(?) p.(Ile441Thr)


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