Variant #0001120394 (NC_000011.9:g.69465966C>T, NM_053056.2:c.804C>T (CCND1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.69465966C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CCND1_000050
Frequency 2/12984
Freq. EA 1/8588
Freq. AA 1/4396
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.804C>T r.(=) p.(=)