Variant #0000306764 (NC_000002.11:g.202149513G>A, NC_000002.11(NM_001228.4):c.854-26G>A (CASP8))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.202149513G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CASP8_000069
Frequency 2/13002
Freq. EA 2/8598
Freq. AA 0/4404
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-04 00:21:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 ?/? c.854-26G>A r.(=) p.(=)