Variant #0000960885 (NC_000009.11:g.139914980G>A, NC_000009.11(NM_001606.4):c.1266-33C>T (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139914980G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000453
Frequency 77/12150
Freq. EA 0/8232
Freq. AA 77/3918
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 10:41:33 +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.1266-33C>T r.(=) p.(=)