List of variants in gene CDK4 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_000075.4(CDK4):c.354+48T>C	rs147481248	0.00340
NM_000075.4(CDK4):c.306A>G (p.Thr102=)	rs201202764	0.00019
NM_000075.4(CDK4):c.-11T>C	rs746754426	0.00011
NM_000075.4(CDK4):c.423G>C (p.Leu141=)	rs760242081	0.00003
NM_000075.4(CDK4):c.549C>T (p.Pro183=)	rs778696237	0.00003
NM_000075.4(CDK4):c.84T>C (p.Ser28=)	rs763203404	0.00003
NM_000075.4(CDK4):c.-32G>T	rs1371795570	0.00001
NM_000075.4(CDK4):c.-9G>T	rs779962297	0.00001
NM_000075.4(CDK4):c.261C>A (p.Ile87=)	rs779482890	0.00001
NM_000075.4(CDK4):c.288A>G (p.Val96=)	rs754092304	0.00001
NM_000075.4(CDK4):c.309T>C (p.Tyr103=)	rs554603181	0.00001
NM_000075.4(CDK4):c.355-12C>T	rs1004281478	0.00001
NM_000075.4(CDK4):c.522+18A>G	rs1555201289	0.00001
NM_000075.4(CDK4):c.-19-56C>G	rs144213234
NM_000075.4(CDK4):c.306A>C (p.Thr102=)	rs201202764
NM_000075.4(CDK4):c.342C>G (p.Ala114=)	rs762471901
NM_000075.4(CDK4):c.534C>G (p.Leu178=)	rs11547327
NM_000075.4(CDK4):c.564G>A (p.Gln188=)	rs1057521685
NM_000075.4(CDK4):c.6T>A (p.Ala2=)	rs1057523632
NM_000075.4(CDK4):c.78C>T (p.Pro26=)	rs1057523487

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