Variant #0001550206 (NC_000017.10:g.7474121G>A, NC_000017.10(NM_015670.5):c.1564+39G>A (SENP3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.7474121G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SENP3_000053
Frequency 1/12062
Freq. EA 0/8236
Freq. AA 1/3826
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 16:02:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SENP3 NM_015670.5 ?/? c.1564+39G>A r.(=) p.(=)