Related gene-specific medical variations for Gene (Select 84240) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334171	NM_001131035.2(ZCCHC9):c.551C>T (p.Ala184Val)	ACOT12, ZCCHC9 (A184V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192575	NM_001131035.2(ZCCHC9):c.496G>C (p.Glu166Gln)	ACOT12, ZCCHC9 (E166Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619897	NM_001131035.2(ZCCHC9):c.652T>C (p.Ser218Pro)	ACOT12, ZCCHC9 (S218P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619896	NM_001131035.2(ZCCHC9):c.612A>T (p.Lys204Asn)	ACOT12, ZCCHC9 (K204N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361079	NM_001131035.2(ZCCHC9):c.527C>T (p.Pro176Leu)	ACOT12, ZCCHC9 (P176L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229935	NM_001131035.2(ZCCHC9):c.634G>A (p.Gly212Ser)	ACOT12, ZCCHC9 (G212S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar