Variant #0000000058 (NC_000024.9:g.4968258A>G, NM_032973.1:c.2639A>G (PCDH11Y))

Chromosome Y
DNA change (genomic) (Relative to hg19 / GRCh37) g.4968258A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PCDH11Y_000010
Frequency 1/2443
Freq. EA 1/1872
Freq. AA 0/571
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 16:16:56 +02:00 (CEST)
Date last edited 2015-04-08 15:48:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PCDH11Y NM_032973.1 ?/? c.2639A>G r.(?) p.(Asn880Ser)