Variant #0000269769 (NC_000002.11:g.202149589G>C, NM_001228.4:c.904G>C (CASP8))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.202149589G>C
DNA change (hg38) g.201284866G>C
Published as CASP8(NM_001080125.2):c.1030G>C (p.D344H)
ISCN -
DB-ID CASP8_000007
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) 0.08984 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 -/. - c.904G>C r.(?) p.(Asp302His)
ALS2CR12 NM_139163.2 -/. - c.*3789C>G r.(=) p.(=)


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