List of variants in gene CCND2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001759.4(CCND2):c.756G>A (p.Ala252=)	rs145050894	0.00074
NM_001759.4(CCND2):c.455C>A (p.Ala152Glu)	rs199719393	0.00007
NM_001759.4(CCND2):c.*1872G>A
NM_001759.4(CCND2):c.*21GA[3]
NM_001759.4(CCND2):c.*2539C>A
NM_001759.4(CCND2):c.*3991C>T
NM_001759.4(CCND2):c.*412C>T
NM_001759.4(CCND2):c.*769A>G
NM_001759.4(CCND2):c.522G>A (p.Leu174=)
NM_001759.4(CCND2):c.801C>T (p.Asp267=)	rs199959738
NM_001759.4(CCND2):c.812C>T (p.Ser271Leu)	rs776036883

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