Variant #0001550189 (NC_000017.10:g.7468991T>C, NC_000017.10(NM_015670.5):c.1216-43T>C (SENP3))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.7468991T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SENP3_000036
Frequency 1/12392
Freq. EA 0/8328
Freq. AA 1/4064
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SENP3 NM_015670.5 ?/? c.1216-43T>C r.(=) p.(=)