Variant #0000960954 (NC_000009.11:g.139918573T>C, NC_000009.11(NM_001606.4):c.160+22A>G (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139918573T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000522
Frequency 1/12490
Freq. EA 0/8392
Freq. AA 1/4098
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 03:24:54 +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.160+22A>G r.(=) p.(=)