Variant #0000891376 (NC_000009.11:g.21970979C>A, NM_000077.4:c.379G>T (CDKN2A))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.21970979C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CDKN2A_000016
Frequency 71/13002
Freq. EA 0/8596
Freq. AA 71/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2019-09-24 10:50:20 +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.379G>T r.(?) p.(Ala127Ser)