Variant #0000965542 (NC_000010.10:g.282887T>C, NC_000010.10(NM_006624.5):c.516+32T>C (ZMYND11))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.282887T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZMYND11_000022
Frequency 1/13006
Freq. EA 1/8600
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 16:30:47 +02:00 (CEST)
Date last edited 2014-05-02 15:45:28 +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.516+32T>C r.(=) p.(=)