"Revvity Omics, Revvity"[submitter] AND "ZFPM2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1061068	NM_012082.4(ZFPM2):c.121C>G (p.Pro41Ala)	ZFPM2 (P41A)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 6129	NM_012082.4(ZFPM2):c.334C>T (p.Arg112Ter)	ZFPM2 (R112* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic/Likely pathogenic
Select item 477991	NM_012082.4(ZFPM2):c.364G>T (p.Val122Leu)	ZFPM2 (V122L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2438649	NM_012082.4(ZFPM2):c.665G>A (p.Arg222His)	ZFPM2, ZFPM2-AS1 (R169H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2438648	NM_012082.4(ZFPM2):c.848T>C (p.Val283Ala)	ZFPM2, ZFPM2-AS1 (V151A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2301127	NM_012082.4(ZFPM2):c.1349C>T (p.Thr450Met)	ZFPM2, ZFPM2-AS1 (T318M +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 644327	NM_012082.4(ZFPM2):c.1889C>T (p.Thr630Ile)	ZFPM2, ZFPM2-AS1 (T498I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance

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