Variant #0000017143 (NC_000001.10:g.171061871G>T, NM_001002294.2:c.72G>T (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.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 -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-03-09 21:11:03 +01:00 (CET)
Date last edited 2017-04-05 10:58:51 +02:00 (CEST)
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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)


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