Variant #0001120361 (NC_000011.9:g.69458012C>T, NM_053056.2:c.412C>T (CCND1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.69458012C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCND1_000017
Frequency 2/12912
Freq. EA 2/8560
Freq. AA 0/4352
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 23:38:10 +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.412C>T r.(=) p.(=)