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

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 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Ian Phillips
Database submission license No license selected
Created by Ian Phillips
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.(=)