Variant #0000017143 (NC_000001.10:g.171061871G>T, FMO3(NM_001002294.2):c.72G>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.171061871G>T
DNA change (hg38) g.171092730G>T
Published as g.72G>T
ISCN -
DB-ID FMO3_000034 See all 2 reported entries
Variant remarks -
Reference PubMed: Koukouritaki et al. 2005, PubMed: Koukouritaki et al. 2007
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency 2/400 chromosomes (non-Latino white), 0/404 (Hispanic American), 0/402 (African American)
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/- 2 c.72G>T - r.(?) p.(Glu24Asp)