Variant #0001550192 (NC_000017.10:g.7469026C>T, NC_000017.10(NM_015670.5):c.1216-8C>T (SENP3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.7469026C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SENP3_000039
Frequency 1/12414
Freq. EA 1/8352
Freq. AA 0/4062
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 16:02:09 +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.1216-8C>T r.(=) p.(=)