Variant #0000989612 (NC_000010.10:g.52576068G>A, NC_000010.10(NM_014576.3):c.868-29C>T (A1CF))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.52576068G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1CF_000044
Frequency 10098/13006
Freq. EA 7317/8600
Freq. AA 2781/4406
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 2018-08-23 00:25:40 +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.868-29C>T r.(=) p.(=)