Related gene-specific medical variations for Gene (Select 10336) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235784	NM_006315.7(PCGF3):c.475_480del (p.Leu159_Glu160del)	PCGF3, PCGF3-AS1	Deletion (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 3210190	NM_006315.7(PCGF3):c.686C>T (p.Ala229Val)	LOC129991957, PCGF3-AS1 +1 more (A229V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615900	NM_006315.7(PCGF3):c.500G>A (p.Arg167His)	PCGF3, PCGF3-AS1 (R133H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 930979	NM_006315.7(PCGF3):c.640C>T (p.His214Tyr)	LOC107986211, PCGF3 +1 more (H214Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	See cases	GUncertain significance
Select item 785081	NM_006315.7(PCGF3):c.540G>A (p.Ala180=)	PCGF3, PCGF3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 769626	NM_006315.7(PCGF3):c.582C>T (p.Asn194=)	PCGF3, PCGF3-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

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