Variant #0000965532 (NC_000010.10:g.256013_256014del, NC_000010.10(NM_006624.5):c.276+25_276+26del (ZMYND11))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.256013_256014del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZMYND11_000011
Frequency 1/12518
Freq. EA 0/8254
Freq. AA 1/4264
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 16:30:47 +02:00 (CEST)
Date last edited 2014-05-03 19:40:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZMYND11 NM_006624.5 ?/? c.276+25_276+26del r.(=) p.(=)