Variant #0000960890 (NC_000009.11:g.139915216G>A, NM_001606.4:c.1195C>T (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139915216G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000458
Frequency 27/12206
Freq. EA 0/8206
Freq. AA 27/4000
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 04:38:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA2 NM_001606.4 ?/? c.1195C>T r.(=) p.(=)