Variant #0000891382 (NC_000009.11:g.21971038C>T, NM_000077.4:c.320G>A (CDKN2A))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.21971038C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CDKN2A_000022
Frequency 1/12970
Freq. EA 1/8576
Freq. AA 0/4394
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 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 16:24:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 ?/? c.320G>A r.(?) p.(Arg107His)