Variant #0000314468 (NC_000002.11:g.215914569T>C, NC_000002.11(NM_173076.2):c.508-34A>G (ABCA12))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.215914569T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA12_000420
Frequency 1/12996
Freq. EA 0/8592
Freq. AA 1/4404
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 16:22:05 +02:00 (CEST)
Date last edited 2018-08-23 05:14:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA12 NM_173076.2 ?/? c.508-34A>G r.(=) p.(=)