Variant #0000989578 (NC_000010.10:g.52566612G>A, NM_014576.3:c.1638C>T (A1CF))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.52566612G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1CF_000016
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:30:47 +02:00 (CEST)
Date last edited 2024-04-30 12:52:47 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1CF NM_014576.3 ?/? c.1638C>T r.(=) p.(=)