Variant #0001623772 (NC_000017.10:g.67031369T>C, NC_000017.10(NM_080283.3):c.1128+18A>G (ABCA9))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.67031369T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCA9_000265
Frequency 12272/13006
Freq. EA 8246/8600
Freq. AA 4026/4406
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 2021-08-19 11:45:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA9 NM_080283.3 ?/? c.1128+18A>G r.(=) p.(=)