"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "HECTD4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 773266	NM_001388303.1(HECTD4):c.13083G>A (p.Pro4361=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2643334	NM_001388303.1(HECTD4):c.12726G>A (p.Ala4242=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3026058	NM_001388303.1(HECTD4):c.12210C>T (p.Ser4070=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643335	NM_001388303.1(HECTD4):c.11328G>A (p.Pro3776=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2643336	NM_001388303.1(HECTD4):c.10726C>G (p.Leu3576Val)	HECTD4 (L3576V +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2643337	NM_001388303.1(HECTD4):c.6984A>G (p.Ala2328=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643338	NM_001388303.1(HECTD4):c.4864G>A (p.Val1622Met)	HECTD4 (V1622M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2643339	NM_001388303.1(HECTD4):c.300G>T (p.Leu100=)	HECTD4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar