List of variants in gene CCND2 reported as pathogenic for central nervous system malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001759.4(CCND2):c.841C>T (p.Pro281Ser)	rs587777621	0.00001
NM_001759.4(CCND2):c.842C>T (p.Pro281Leu)	rs587777622	0.00001
NM_001759.4(CCND2):c.808A>T (p.Lys270Ter)	rs587777619
NM_001759.4(CCND2):c.838A>C (p.Thr280Pro)
NM_001759.4(CCND2):c.838A>G (p.Thr280Ala)	rs587777618
NM_001759.4(CCND2):c.839C>A (p.Thr280Asn)	rs587777620
NM_001759.4(CCND2):c.842C>G (p.Pro281Arg)	rs587777622

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