Variant #0000891392 (NC_000009.11:g.21974451_21974460del, NC_000009.11(NM_000077.4):c.150+217_150+226del (CDKN2A))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.21974451_21974460del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CDKN2A_000032
Frequency 113/12518
Freq. EA 3/8254
Freq. AA 110/4264
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 16:24:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 ?/? c.150+217_150+226del r.(=) p.(=)