CCNI[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2508495	NM_006835.3(CCNI):c.899T>C (p.Val300Ala)	CCNI (V257A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267845	NM_006835.3(CCNI):c.733C>T (p.His245Tyr)	CCNI (H204Y +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139938	NM_006835.3(CCNI):c.616A>G (p.Met206Val)	CCNI (M101V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550162	NM_006835.3(CCNI):c.568G>A (p.Ala190Thr)	CCNI (A75T +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3139937	NM_006835.3(CCNI):c.238G>A (p.Val80Ile)	CCNI (V66I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2220488	NM_006835.3(CCNI):c.179A>G (p.Asn60Ser)	CCNI (N46S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar