Variant #0000238702 (NC_000002.11:g.69741586C>T, NC_000002.11(NM_014911.3):c.1776+17G>A (AAK1))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.69741586C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAK1_000081
Frequency 2/11352
Freq. EA 2/7488
Freq. AA 0/3864
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 16:22:05 +02:00 (CEST)
Date last edited 2018-08-23 03:53:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAK1 NM_014911.3 ?/? c.1776+17G>A r.(=) p.(=)