Variant #0000992370 (NC_000002.11:g.202131489G>C, NM_001228.4:c.280G>C (CASP8))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.202131489G>C
DNA change (hg38) -
Published as CASP8(NM_001080125.2):c.457G>C (p.G153R), CASP8(NM_001228.4):c.280G>C (p.G94R)
ISCN -
DB-ID CASP8_000032 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 ?/. - c.280G>C r.(?) p.(Gly94Arg)


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