Variant #0001685362 (NC_000019.9:g.1043238G>T, NM_019112.3:c.778G>T (ABCA7))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.1043238G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA7_000063
Frequency 1/13002
Freq. EA 1/8598
Freq. AA 0/4404
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 16:45:39 +02:00 (CEST)
Date last edited 2018-08-23 01:54:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ?/? c.778G>T r.(?) p.(Asp260Tyr)