"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "MTMR2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1163341	NM_016156.6(MTMR2):c.1712G>A (p.Arg571His)	MTMR2 (R499H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 234456	NM_016156.6(MTMR2):c.1336G>A (p.Glu446Lys)	MTMR2 (E446K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +4 more	GConflicting classifications of pathogenicity
Select item 1163342	NM_016156.6(MTMR2):c.1278G>A (p.Gln426=)	MTMR2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 476877	NM_016156.6(MTMR2):c.894A>T (p.Glu298Asp)	MTMR2 (E298D +1 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease type 4B1 +4 more	GUncertain significance
Select item 1163343	NM_016156.6(MTMR2):c.796C>T (p.Arg266Cys)	MTMR2 (R194C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2683165	NM_016156.6(MTMR2):c.277T>C (p.Tyr93His)	MTMR2 (Y21H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1163344	NM_016156.6(MTMR2):c.64G>A (p.Val22Met)	MTMR2 (V22M)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GUncertain significance

ClinVar