Related gene-specific medical variations for Gene (Select 374659) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645716	NM_001286451.2(HDDC3):c.414G>A (p.Trp138Ter)	HDDC3, UNC45A (W138*)	Single nucleotide variant (nonsense +3 more)	not provided	GLikely benign
Select item 2483679	NM_001286451.2(HDDC3):c.332G>A (p.Ser111Asn)	HDDC3, LOC130057951 +1 more (S111N)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance