Variant #0000965539 (NC_000010.10:g.282762_282763insT, NC_000010.10(NM_006624.5):c.439-16_439-15insT (ZMYND11))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.282762_282763insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZMYND11_000018
Frequency 55/12514
Freq. EA 36/8250
Freq. AA 19/4264
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 21:15:40 +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.439-16_439-15insT r.(=) p.(=)