"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CDK4"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 219393	NM_000075.4(CDK4):c.771G>A (p.Val257=)	CDK4, TSPAN31	Single nucleotide variant (synonymous variant +1 more)	Familial melanoma +3 more	GBenign/Likely benign
Select item 133876	NM_000075.4(CDK4):c.661G>A (p.Asp221Asn)	CDK4, TSPAN31 (D221N)	Single nucleotide variant (missense variant +1 more)	Melanoma, cutaneous malignant, susceptibility to, 3 +4 more	GConflicting classifications of pathogenicity
Select item 483284	NM_000075.4(CDK4):c.481C>T (p.Leu161=)	CDK4	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign
Select item 381622	NM_000075.4(CDK4):c.309T>C (p.Tyr103=)	CDK4	Single nucleotide variant (synonymous variant)	Familial melanoma +3 more	GLikely benign
Select item 386089	NM_000075.4(CDK4):c.306A>C (p.Thr102=)	CDK4	Single nucleotide variant (synonymous variant)	Familial melanoma +3 more	GLikely benign
Select item 309983	NM_000075.4(CDK4):c.-60C>G	CDK4	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign
Select item 309985	NM_000075.4(CDK4):c.-123T>G	CDK4	Single nucleotide variant (5 prime UTR variant)	Melanoma, cutaneous malignant, susceptibility to, 3 +2 more	GConflicting classifications of pathogenicity
Select item 2498574	GRCh37/hg19 12q13.3-14.1(chr12:57064059-59314016)x1	PIP4K2C, SDR9C7 +45 more	Copy number loss	not provided	GLikely pathogenic

ClinVar