"PreventionGenetics, part of Exact Sciences"[submitter] AND "MME"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1221640	NM_007289.4(MME):c.22A>G (p.Met8Val)	MME (M8V)	Single nucleotide variant (missense variant)	MME-related condition +1 more	GBenign
Select item 1559411	NM_007289.4(MME):c.96G>A (p.Ser32=)	MME	Single nucleotide variant (synonymous variant)	MME-related condition +1 more	GLikely benign
Select item 2629115	NM_007289.4(MME):c.844G>T (p.Glu282Ter)	MME (E282*)	Single nucleotide variant (nonsense)	MME-related condition	GLikely pathogenic
Select item 2632036	NM_007289.4(MME):c.1250G>A (p.Gly417Glu)	MME (G417E)	Single nucleotide variant (missense variant)	MME-related condition	GUncertain significance
Select item 1699816	NM_007289.4(MME):c.1559G>C (p.Ser520Thr)	MME (S520T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3000253	NM_007289.4(MME):c.1645G>T (p.Gly549Ter)	MME (G549*)	Single nucleotide variant (nonsense)	MME-related condition +1 more	GPathogenic
Select item 1635700	NM_007289.4(MME):c.1778A>G (p.Asn593Ser)	MME (N593S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 707888	NM_007289.4(MME):c.2133G>A (p.Val711=)	MME	Single nucleotide variant (synonymous variant)	MME-related condition +3 more	GBenign/Likely benign

ClinVar