Variant #0000960889 (NC_000009.11:g.139915178G>T, NM_001606.4:c.1233C>A (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139915178G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA2_000457
Frequency 1/12218
Freq. EA 0/8222
Freq. AA 1/3996
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 04:27:35 +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.1233C>A r.(=) p.(=)