Variant #0000019220 (NC_000001.10:g.171254485A>G, NM_002021.1:c.1401A>G (FMO1))

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.171254485A>G
DNA change (hg38) g.171285346A>G
Published as 27258A>G
ISCN -
DB-ID FMO1_000008
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs28360432
Origin Germline
Segregation -
Frequency 0.02 in Chinese
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00261 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-07-28 13:09:14 +02:00 (CEST)
Date last edited 2017-04-04 22:34:36 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Enzyme activity     
FMO1 NM_002021.1 ?/? 9 c.1401A>G - r.(?) p.(Pro467=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.