Variant #0000921465 (NC_000009.11:g.107651526A>G, NC_000009.11(NM_005502.3):c.67-50T>C (ABCA1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.107651526A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA1_000439
Frequency 2500/13004
Freq. EA 1266/8600
Freq. AA 1234/4404
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 16:29:58 +02:00 (CEST)
Date last edited 2019-09-14 14:08:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA1 NM_005502.3 ?/? c.67-50T>C r.(=) p.(=)