Variant #0001120390 (NC_000011.9:g.69465873_69465876del, NC_000011.9(NM_053056.2):c.724-13_724-10del (CCND1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.69465873_69465876del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCND1_000046
Frequency 28/12486
Freq. EA 23/8244
Freq. AA 5/4242
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 23:38:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CCND1 NM_053056.2 ?/? c.724-13_724-10del r.(=) p.(=)