"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130056 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 744019	NM_138477.4(CDAN1):c.483C>T (p.Arg161=)	CDAN1, LOC130056931	Single nucleotide variant (synonymous variant)	CDAN1-related condition +1 more	GLikely benign
Select item 262378	NM_138477.4(CDAN1):c.477C>T (p.Pro159=)	CDAN1, LOC130056931	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 262377	NM_138477.4(CDAN1):c.443C>T (p.Ala148Val)	CDAN1, LOC130056931 (A148V)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 2916985	NM_138477.4(CDAN1):c.327C>G (p.Thr109=)	CDAN1, LOC130056931	Single nucleotide variant (synonymous variant)	CDAN1-related condition +1 more	GLikely benign
Select item 21751	NM_138477.4(CDAN1):c.320A>T (p.Gln107Leu)	CDAN1, LOC130056931 (Q107L)	Single nucleotide variant (missense variant)	Anemia, congenital dyserythropoietic, type 1a +3 more	GBenign
Select item 2635130	NM_138477.4(CDAN1):c.289C>A (p.Arg97Ser)	CDAN1, LOC130056931 (R97S)	Single nucleotide variant (missense variant)	CDAN1-related condition	GUncertain significance

ClinVar