Variant #0001623484 (NC_000017.10:g.66929382T>G, NM_007168.2:c.497A>C (ABCA8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.66929382T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA8_000322
Frequency 13/13002
Freq. EA 0/8596
Freq. AA 13/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2018-08-23 05:23:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA8 NM_007168.2 ?/? c.497A>C r.(?) p.(Tyr166Ser)