Variant #0000000077 (NC_000024.9:g.6115366C>T, NC_000024.9(NM_022573.2):c.487-31C>T (TSPY2))

Chromosome Y
DNA change (genomic) (Relative to hg19 / GRCh37) g.6115366C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSPY2_000001
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 2014-03-13 18:59:53 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSPY2 NM_022573.2 ?/? c.487-31C>T r.(=) p.(=)