Variant #0000639188 (NC_000006.11:g.31856712C>A, NC_000006.11(NM_006709.3):c.1216+34G>T (EHMT2))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.31856712C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID EHMT2_000131
Frequency 82/12886
Freq. EA 48/8552
Freq. AA 34/4334
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 16:27:59 +02:00 (CEST)
Date last edited 2013-05-04 09:08:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
EHMT2 NM_006709.3 ?/? c.1216+34G>T r.(=) p.(=)