Variant #0000800273 (NC_000002.11:g.202149917C>T, NM_001228.4:c.1232C>T (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.202149917C>T
DNA change (hg38) -
Published as CASP8(NM_001080125.1):c.1358C>T (p.P453L)
ISCN -
DB-ID ALS2CR12_000003
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP8 NM_001228.4 ?/. - c.1232C>T r.(?) p.(Pro411Leu)
ALS2CR12 NM_139163.2 ?/. - c.*3461G>A r.(=) p.(=)


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