Variant #0000799116 (NC_000007.13:g.148516828_148516829del, NC_000007.13(NM_001203247.1):c.893-50_893-49del (EZH2))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.148516828_148516829del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID EZH2_000083
Frequency 1/12514
Freq. EA 1/8254
Freq. AA 0/4260
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 13:42:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
EZH2 NM_001203247.1 ?/? c.893-50_893-49del r.(=) p.(=)