Variant #0001667607 (NC_000018.9:g.42391312T>C, NC_000018.9(NM_001130110.1):c.487-57883T>C (SETBP1))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.42391312T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SETBP1_000059
Frequency 16/4566
Freq. EA 0/3182
Freq. AA 16/1384
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 20:54:35 +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.487-57883T>C r.(=) p.(=)