Variant #0000960916 (NC_000009.11:g.139916486_139916493del, NC_000009.11(NM_001606.4):c.568-40_568-33del (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139916486_139916493del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000482
Frequency 3487/10790
Freq. EA 2345/7362
Freq. AA 1142/3428
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 2018-08-23 00:30:17 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA2 NM_001606.4 ?/? c.568-40_568-33del r.(=) p.(=)