"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "CCDC88C"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2175555	NM_001080414.4(CCDC88C):c.4544T>C (p.Leu1515Pro)	CCDC88C (L1515P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380231	NM_001080414.4(CCDC88C):c.4397A>G (p.Asn1466Ser)	CCDC88C (N1466S)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 3380232	NM_001080414.4(CCDC88C):c.3690G>C (p.Leu1230Phe)	CCDC88C (L1230F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3380233	NM_001080414.4(CCDC88C):c.3641G>T (p.Gly1214Val)	CCDC88C (G1214V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2429549	NM_001080414.4(CCDC88C):c.1235T>C (p.Leu412Pro)	CCDC88C (L412P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 723630	NM_001080414.4(CCDC88C):c.483+8C>T	CCDC88C	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity

ClinVar