Variant #0000019556 (NC_000001.10:g.171059257T>A, NM_001002294.2:c.-872T>A (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.171059257T>A
DNA change (hg38) g.171090116T>A
Published as -2543T>A
ISCN -
DB-ID FMO3_000097
Variant remarks no effect on transcription in vitro
Reference PubMed: Koukouritaki et al. 2005
ClinVar ID -
dbSNP ID rs12404218
Origin Germline
Segregation ?
Frequency HapMap 0.066 (Eur), 0.256 (Jpn), 0.080 (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 15:56:10 +02:00 (CEST)
Date last edited 2017-04-05 11:00:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/- _1 c.-872T>A - r.(=) p.(=)


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