"CCND2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3036591	NM_001759.4(CCND2):c.33C>T (p.Val11=)	CCND2, CCND2-AS1	Single nucleotide variant (synonymous variant)	CCND2-related condition	GLikely benign
Select item 1280861	NM_001759.4(CCND2):c.114T>G (p.Leu38=)	CCND2, CCND2-AS1	Single nucleotide variant (synonymous variant)	CCND2-related condition +1 more	GBenign/Likely benign
Select item 507274	NM_001759.4(CCND2):c.524C>G (p.Ser175Cys)	CCND2 (S175C)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 3043450	NM_001759.4(CCND2):c.572-4G>T	CCND2	Single nucleotide variant (intron variant)	CCND2-related condition	GLikely benign
Select item 391416	NM_001759.4(CCND2):c.597G>A (p.Pro199=)	CCND2	Single nucleotide variant (synonymous variant)	CCND2-related condition +1 more	GLikely benign
Select item 3054551	NM_001759.4(CCND2):c.702G>A (p.Lys234=)	CCND2	Single nucleotide variant (synonymous variant)	CCND2-related condition	GLikely benign
Select item 511836	NM_001759.4(CCND2):c.756G>A (p.Ala252=)	CCND2	Single nucleotide variant (synonymous variant)	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 +2 more	GBenign/Likely benign
Select item 143985	NM_001759.4(CCND2):c.842C>G (p.Pro281Arg)	CCND2 (P281R)	Single nucleotide variant (missense variant)	CCND2-related condition +1 more	GConflicting classifications of pathogenicity
Select item 3061433	NM_001759.4(CCND2):c.853C>A (p.Arg285=)	CCND2	Single nucleotide variant (synonymous variant)	CCND2-related condition	GLikely benign