All variants in the CASP8AP2 gene

Information The variants shown are described using the NM_001137667.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.632C>T r.(?) p.(Thr211Ile) - likely benign g.90572060C>T g.89862341C>T CASP8AP2(NM_001137667.1):c.632C>T (p.(Thr211Ile)) - CASP8AP2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
?/. - c.4343C>T r.(?) p.(Ser1448Leu) - VUS g.90577352C>T g.89867633C>T CASP8AP2(NM_001137667.1):c.4343C>T (p.(Ser1448Leu)) - CASP8AP2_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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