Related gene-specific medical variations for Gene (Select 84517) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3142867	NM_032487.5(ACTRT3):c.245A>T (p.Glu82Val)	ACTRT3, LOC128772257 (E82V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2654270	NM_032487.5(ACTRT3):c.110G>T (p.Arg37Leu)	ACTRT3, LOC129937872 (R37L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2484804	NM_032487.5(ACTRT3):c.109C>G (p.Arg37Gly)	ACTRT3, LOC129937872 (R37G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457478	NM_032487.5(ACTRT3):c.127C>A (p.Arg43Ser)	ACTRT3, LOC129937872 (R43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291153	NM_032487.5(ACTRT3):c.68G>T (p.Gly23Val)	ACTRT3, LOC129937872 (G23V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213267	NM_032487.5(ACTRT3):c.152T>G (p.Leu51Arg)	ACTRT3, LOC129937872 (L51R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar