Variant #0001644239 (NC_000017.10:g.79099219A>G, NC_000017.10(NM_004920.2):c.447-405T>C (AATK))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.79099219A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AATK_000158
Frequency 4/10224
Freq. EA 0/7134
Freq. AA 4/3090
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 12:48:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATK NM_004920.2 ?/? c.447-405T>C r.(=) p.(=)