Related gene-specific medical variations for Gene (Select 166968) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126457	NM_001297599.2(MIER3):c.1283G>A (p.Arg428His)	MIER3, SETD9 (R433H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614825	NM_001297599.2(MIER3):c.1616A>G (p.His539Arg)	MIER3, SETD9 (H539R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597983	NM_001297599.2(MIER3):c.1225G>A (p.Asp409Asn)	MIER3, SETD9 (D408N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2555499	NM_001297599.2(MIER3):c.1058A>G (p.Tyr353Cys)	MIER3, SETD9 (Y353C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554707	NM_001297599.2(MIER3):c.1353T>G (p.Asp451Glu)	MIER3, SETD9 (D451E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362613	NM_001297599.2(MIER3):c.1410G>A (p.Met470Ile)	MIER3, SETD9 (M469I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324841	NM_001297599.2(MIER3):c.1231A>T (p.Thr411Ser)	MIER3, SETD9 (T410S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299099	NM_001297599.2(MIER3):c.1400C>G (p.Pro467Arg)	MIER3, SETD9 (P472R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance