Variant #0000306759 (NC_000002.11:g.202139682C>T, NC_000002.11(NM_001228.4):c.711+6C>T (CASP8))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.202139682C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CASP8_000059
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 ?/? c.711+6C>T r.(=) p.(=)