"Clinical Genetics, Academic Medical Center"[submitter] AND "CDON"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 260799	NM_001378964.1(CDON):c.3662T>A (p.Ile1221Asn)	CDON (I1221N +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 260797	NM_001378964.1(CDON):c.3549C>T (p.Val1183=)	CDON	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 260793	NM_001378964.1(CDON):c.3294G>A (p.Thr1098=)	CDON	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 260792	NM_001378964.1(CDON):c.3165T>C (p.Asn1055=)	CDON	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 260791	NM_001378964.1(CDON):c.3039C>T (p.Asn1013=)	CDON	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 260784	NM_001378964.1(CDON):c.2037G>A (p.Ala679=)	CDON	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 95752	NM_001378964.1(CDON):c.223G>A (p.Val75Ile)	CDON (V75I)	Single nucleotide variant (missense variant)	Holoprosencephaly 11 +2 more	GBenign

ClinVar