"CSNK2A1-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1249520	NM_177559.3(CSNK2A1):c.*2G>A	CSNK2A1	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 2630977	NM_177559.3(CSNK2A1):c.990C>A (p.Asp330Glu)	CSNK2A1 (D194E +1 more)	Single nucleotide variant (missense variant)	CSNK2A1-related disorder	GUncertain significance
Select item 2630140	NM_177559.3(CSNK2A1):c.941C>G (p.Thr314Ser)	CSNK2A1 (T178S +1 more)	Single nucleotide variant (missense variant)	CSNK2A1-related disorder	GUncertain significance
Select item 1327181	NM_177559.3(CSNK2A1):c.400C>T (p.Arg134Ter)	CSNK2A1 (R134*)	Single nucleotide variant (nonsense +1 more)	CSNK2A1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 713025	NM_177559.3(CSNK2A1):c.369A>G (p.Gln123=)	CSNK2A1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1297057	NM_177559.3(CSNK2A1):c.319C>T (p.Arg107Ter)	CSNK2A1 (R107*)	Single nucleotide variant (nonsense +1 more)	CSNK2A1-related disorder +1 more	GLikely pathogenic

ClinVar