Variant #0000799068 (NC_000007.13:g.148511116C>T, NM_001203247.1:c.1771G>A (EZH2))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.148511116C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID EZH2_000035
Frequency 4/13006
Freq. EA 4/8600
Freq. AA 0/4406
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 13:42:04 +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.1771G>A r.(?) p.(Ala591Thr)