"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCND1"[ge - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034107	NM_053056.3(CCND1):c.649C>T (p.Leu217=)	CCND1	Single nucleotide variant (synonymous variant)	CCND1-related disorder	GLikely benign
Select item 1250573	NM_053056.3(CCND1):c.669C>T (p.Phe223=)	CCND1	Single nucleotide variant (synonymous variant)	CCND1-related disorder +1 more	GBenign
Select item 3050562	NM_053056.3(CCND1):c.714G>A (p.Lys238=)	CCND1	Single nucleotide variant (synonymous variant)	CCND1-related disorder	GLikely benign
Select item 13755	NM_053056.3(CCND1):c.723G>A (p.Pro241=)	CCND1	Single nucleotide variant (synonymous variant)	CCND1-related disorder +1 more	GBenign
Select item 3038710	NM_053056.3(CCND1):c.827AGG[4] (p.Glu280del)	CCND1 (E280del)	Microsatellite (inframe_indel +1 more)	CCND1-related disorder	GLikely benign

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