Variant #0000306784 (NC_000002.11:g.202151330_202151331insTTTGT, NM_001228.4:c.*13_*14insTTTGT (CASP8))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.202151330_202151331insTTTGT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CASP8_000082
Frequency 46/12520
Freq. EA 10/8254
Freq. AA 36/4266
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 00:21:34 +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.*13_*14insTTTGT r.(=) p.(=)