"PreventionGenetics, part of Exact Sciences"[submitter] AND "CPB2-AS1" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035536	NM_001872.5(CPB2):c.1215T>C (p.Cys405=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant)	CPB2-related condition	GLikely benign
Select item 3058934	NM_001872.5(CPB2):c.1040T>C (p.Ile347Thr)	CPB2, CPB2-AS1 (I310T +1 more)	Single nucleotide variant (missense variant)	CPB2-related condition	GBenign
Select item 3059439	NM_001872.5(CPB2):c.753C>T (p.Ile251=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant)	CPB2-related condition	GBenign
Select item 3059117	NM_001872.5(CPB2):c.678T>C (p.Asp226=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant +1 more)	CPB2-related condition	GBenign
Select item 3060410	NM_001872.5(CPB2):c.663A>G (p.Pro221=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant +1 more)	CPB2-related condition	GBenign
Select item 3039073	NM_001872.5(CPB2):c.552A>G (p.Glu184=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant)	CPB2-related condition	GLikely benign
Select item 3059667	NM_001872.5(CPB2):c.505G>A (p.Ala169Thr)	CPB2, CPB2-AS1 (A169T)	Single nucleotide variant (missense variant)	CPB2-related condition	GBenign
Select item 3060878	NM_001872.5(CPB2):c.291T>C (p.Asp97=)	CPB2, CPB2-AS1	Single nucleotide variant (synonymous variant)	CPB2-related condition	GBenign

ClinVar