Variant #0001623482 (NC_000017.10:g.66929299T>G, NC_000017.10(NM_007168.2):c.570+10A>C (ABCA8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.66929299T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA8_000320
Frequency 1/12998
Freq. EA 1/8592
Freq. AA 0/4406
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 06:56:14 +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.570+10A>C r.(=) p.(=)