Variant #0001506358 (NC_000016.9:g.68855852G>C, NC_000016.9(NM_004360.3):c.1712-52G>C (CDH1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.68855852G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CDH1_000094
Frequency 116/5734
Freq. EA 105/3982
Freq. AA 11/1752
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 14:20:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CDH1 NM_004360.3 ?/? c.1712-52G>C r.(=) p.(=)