Variant #0001468446 (NC_000016.9:g.16315658C>A, NM_001079528.3:c.67G>T (ABCC6))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16315658C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC6_000010
Frequency 1/12284
Freq. EA 1/8182
Freq. AA 0/4102
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 16:42:42 +02:00 (CEST)
Date last edited 2018-09-30 11:53:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC6 NM_001079528.3 ?/? c.67G>T r.(?) p.(Ala23Ser)