Variant #0000607387 (NC_000002.11:g.202139619G>C, NM_001228.4:c.654G>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.202139619G>C
DNA change (hg38) g.201274896G>C
Published as CASP8(NM_001080125.1):c.780G>C (p.E260D), CASP8(NM_001080125.2):c.780G>C (p.E260D)
ISCN -
DB-ID CASP8_000020 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 ?/. - c.654G>C r.(?) p.(Glu218Asp)


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