Variant #0000965543 (NC_000010.10:g.282897C>T, NC_000010.10(NM_006624.5):c.516+42C>T (ZMYND11))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.282897C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZMYND11_000024
Frequency 12121/13006
Freq. EA 8415/8600
Freq. AA 3706/4406
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 2025-01-04 16:59:10 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZMYND11 NM_006624.5 ?/? c.516+42C>T r.(=) p.(=)