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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2460275	NM_001039618.4(CREBZF):c.848G>A (p.Arg283Gln)	CREBZF (R283Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077364	NM_001039618.4(CREBZF):c.482A>C (p.Asp161Ala)	CREBZF (D161A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 746876	NM_001039618.4(CREBZF):c.363C>T (p.Asp121=)	CREBZF	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3077363	NM_001039618.4(CREBZF):c.293A>T (p.Asp98Val)	CREBZF (D98V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276420	NM_001039618.4(CREBZF):c.236C>A (p.Ser79Tyr)	CREBZF (S79Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495355	NM_001039618.4(CREBZF):c.122G>T (p.Gly41Val)	CREBZF (G41V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517047	NM_001039618.4(CREBZF):c.121G>C (p.Gly41Arg)	CREBZF (G41R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077368	NM_001039618.4(CREBZF):c.76G>A (p.Ala26Thr)	CREBZF (A26T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar