Related gene-specific medical variations for Gene (Select 130004338) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3104938	NM_182765.6(HECTD2):c.88G>C (p.Glu30Gln)	HECTD2, HECTD2-AS1 +1 more (E30Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3104933	NM_182765.6(HECTD2):c.119C>T (p.Ala40Val)	HECTD2, HECTD2-AS1 +1 more (A40V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2554438	NM_182765.6(HECTD2):c.112G>C (p.Val38Leu)	HECTD2, HECTD2-AS1 +1 more (V38L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472384	NM_182765.6(HECTD2):c.94G>C (p.Glu32Gln)	HECTD2, HECTD2-AS1 +1 more (E32Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459818	NM_182765.6(HECTD2):c.19G>C (p.Val7Leu)	HECTD2, HECTD2-AS1 +1 more (V7L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2222576	NM_182765.6(HECTD2):c.31G>T (p.Ala11Ser)	HECTD2, HECTD2-AS1 +1 more (A11S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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