Variant #0000019560 (NC_000001.10:g.171059839T>C, FMO3(NM_001002294.2):c.-290T>C)

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.171059839T>C
DNA change (hg38) g.171090698T>C
Published as -1961T>C
ISCN -
DB-ID FMO3_000101
Variant remarks no effect on transcription in vitro
Reference PubMed: Koukouritaki et al. 2005
ClinVar ID -
dbSNP ID rs16864007
Origin Germline
Segregation ?
Frequency HapMap 0.000 (Eur), 0.000 (Asian), 0.031 (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.-290T>C - r.(=) p.(=)