Related gene-specific medical variations for Gene (Select 27252) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3360948	NM_014458.4(KLHL20):c.1699T>G (p.Tyr567Asp)	KLHL20 (Y567D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359907	NM_014458.4(KLHL20):c.1547A>T (p.Asp516Val)	KLHL20 (D516V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 161677	NM_014458.4(KLHL20):c.257del (p.Leu86fs)	KLHL20 (L86fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance

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