Variant #0000989641 (NC_000010.10:g.52601793G>T, NC_000010.10(NM_014576.3):c.235-41C>A (A1CF))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.52601793G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1CF_000073
Frequency 2/12990
Freq. EA 0/8588
Freq. AA 2/4402
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 2024-12-29 05:15:37 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1CF NM_014576.3 ?/? c.235-41C>A r.(=) p.(=)