Variant #0000989616 (NC_000010.10:g.52587868C>A, NC_000010.10(NM_014576.3):c.769+23G>T (A1CF))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.52587868C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1CF_000048
Frequency 1/13000
Freq. EA 0/8594
Freq. AA 1/4406
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 2024-04-28 01:06:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1CF NM_014576.3 ?/? c.769+23G>T r.(=) p.(=)