"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CDC6"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1587110	NM_001254.4(CDC6):c.123C>T (p.Thr41=)	CDC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 808259	NM_001254.4(CDC6):c.148G>C (p.Ala50Pro)	CDC6 (A50P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 210619	NM_001254.4(CDC6):c.165C>T (p.Pro55=)	CDC6	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 323055	NM_001254.4(CDC6):c.597C>G (p.Tyr199Ter)	CDC6 (Y199*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 210621	NM_001254.4(CDC6):c.712A>G (p.Thr238Ala)	CDC6 (T238A)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 128638	NM_001254.4(CDC6):c.883G>A (p.Asp295Asn)	CDC6 (D295N)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 369837	GRCh37/hg19 17q21.2(chr17:38456598-38456659)x1	CDC6	Copy number loss	not provided	GLikely pathogenic

ClinVar