MIER3[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2484184	NM_001297599.2(MIER3):c.602A>G (p.Glu201Gly)	MIER3 (E201G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539223	NM_001297599.2(MIER3):c.511G>A (p.Asp171Asn)	MIER3 (D171N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294863	NM_001297599.2(MIER3):c.476A>G (p.Glu159Gly)	MIER3 (E164G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311474	NM_001297599.2(MIER3):c.458A>G (p.Asp153Gly)	MIER3 (D158G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294862	NM_001297599.2(MIER3):c.406A>C (p.Thr136Pro)	MIER3 (T136P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126459	NM_001297599.2(MIER3):c.248C>G (p.Ala83Gly)	MIER3 (A88G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126458	NM_001297599.2(MIER3):c.164T>C (p.Ile55Thr)	MIER3 (I60T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360496	NM_001297599.2(MIER3):c.32C>T (p.Pro11Leu)	MIER3 (P11L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar