Variant #0000923556 (NC_000002.11:g.202093655G>C, NM_032977.3:c.*11191G>C (CASP10))

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.202093655G>C
DNA change (hg38) -
Published as CASP10(NM_032974.5):c.1416-1G>C
ISCN -
DB-ID CASP8_000030
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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.-4814G>C r.(?) p.(=)
CASP10 NM_032977.3 ?/. - c.*11191G>C r.(=) p.(=)


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