Variant #0001120388 (NC_000011.9:g.69465860A>G, NC_000011.9(NM_053056.2):c.724-26A>G (CCND1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.69465860A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCND1_000044
Frequency 1799/12948
Freq. EA 156/8578
Freq. AA 1643/4370
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 23:38:11 +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.724-26A>G r.(=) p.(=)