Variant #0000960920 (NC_000009.11:g.139916833T>G, NM_001606.4:c.537A>C (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139916833T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000488
Frequency 1471/12332
Freq. EA 714/8288
Freq. AA 757/4044
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 16:29:58 +02:00 (CEST)
Date last edited 2018-08-22 23:52:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA2 NM_001606.4 ?/? c.537A>C r.(=) p.(=)