Variant #0000019557 (NC_000001.10:g.171059623G>C, NM_001002294.2:c.-506G>C (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.171059623G>C
DNA change (hg38) g.171090482G>C
Published as -2177G>C
ISCN -
DB-ID FMO3_000098
Variant remarks increases transcription in vitro by up to 8-fold, effect in vivo unknown
Reference PubMed: Koukouritaki et al. 2005
ClinVar ID -
dbSNP ID rs3754491
Origin Germline
Segregation ?
Frequency HapMap 0.100 (Eur), 0.244 (Jpn), 0.075 (Afr)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ian Phillips
Database submission license No license selected
Created by Ian Phillips
Date created 2013-08-14 16:04:56 +02:00 (CEST)
Date last edited 2017-04-05 11:00:42 +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 ?/? _1 c.-506G>C - r.(=) p.(=)


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