Variant #0000167068 (NC_000001.10:g.171077348C>T, NM_001002294.2:c.613C>T (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.171077348C>T
DNA change (hg38) g.171108207C>T
Published as -
ISCN -
DB-ID FMO3_000041 See all 8 reported entries
Variant remarks Expected to affect metabolism of drug substrates of FMO3
Reference -
ClinVar ID -
dbSNP ID rs2266782
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00021 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-02-21 16:34:07 +01:00 (CET)
Date last edited 2017-04-05 15:37:06 +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 +/+ 5 c.613C>T - r.(?) p.(Arg205Cys)


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