C4014531[trait identifier] AND "Diagnostic Genetics, Severance Hospita - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1803035	NM_021072.4(HCN1):c.794T>A (p.Leu265His)	HCN1 (L265H)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 24	GLikely pathogenic
Select item 1803037	NM_021072.4(HCN1):c.535A>T (p.Asn179Tyr)	HCN1 (N179Y)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 24	GLikely pathogenic