Variant #0001623496 (NC_000017.10:g.66936942G>T, NM_007168.2:c.258C>A (ABCA8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.66936942G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA8_000334
Frequency 33/13006
Freq. EA 0/8600
Freq. AA 33/4406
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 2025-01-02 07:51:55 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA8 NM_007168.2 ?/? c.258C>A r.(=) p.(=)