Variant #0000019551 (NC_000001.10:g.171076935C>T, FMO3(NM_001002294.2):c.441C>T)

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.171076935C>T
DNA change (hg38) g.171107794C>T
Published as 15019A>C (S147S)
ISCN -
DB-ID FMO3_000092 See all 6 reported entries
Variant remarks -
Reference PubMed: Koukouritaki et al. 2005
ClinVar ID -
dbSNP ID rs1800822
Origin Germline
Segregation no
Frequency HapMap 0.066 (Eur), 0.227 (Jpn), 0.031 (Afr)
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.11445 View details
Owner Ian Phillips
Database submission license No license selected
Created by Ian Phillips
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/- 4 c.441C>T - r.(=) p.(=)