Variant #0001667574 (NC_000018.9:g.42358695_42358697del, NC_000018.9(NM_001130110.1):c.486+76898_486+76900del (SETBP1))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.42358695_42358697del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SETBP1_000026
Frequency 12/6524
Freq. EA 12/4288
Freq. AA 0/2236
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 16:45:07 +02:00 (CEST)
Date last edited 2013-05-05 20:54:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SETBP1 NM_001130110.1 ?/? c.486+76898_486+76900del r.(=) p.(=)