Variant #0000454568 (NC_000004.11:g.132155C>T, NC_000004.11(NM_001039127.3):c.4-1467C>T (ZNF718))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.132155C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF718_000021
Frequency 5/6248
Freq. EA 5/4220
Freq. AA 0/2028
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 16:25:12 +02:00 (CEST)
Date last edited 2014-05-20 08:50:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF718 NM_001039127.3 ?/? c.4-1467C>T r.(=) p.(=)