C4310739[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2440582	NM_177559.3(CSNK2A1):c.955A>G (p.Met319Val)	CSNK2A1 (M183V +1 more)	Single nucleotide variant (missense variant)	Okur-Chung neurodevelopmental syndrome	GUncertain significance
Select item 2440583	NM_177559.3(CSNK2A1):c.809A>G (p.Asn270Ser)	CSNK2A1 (N134S +1 more)	Single nucleotide variant (missense variant)	Okur-Chung neurodevelopmental syndrome	GUncertain significance
Select item 2440584	NM_177559.3(CSNK2A1):c.584G>A (p.Arg195Gln)	CSNK2A1 (R195Q +1 more)	Single nucleotide variant (missense variant)	Okur-Chung neurodevelopmental syndrome	GUncertain significance
Select item 2440586	NM_177559.3(CSNK2A1):c.385A>G (p.Thr129Ala)	CSNK2A1 (T129A)	Single nucleotide variant (missense variant +1 more)	Okur-Chung neurodevelopmental syndrome	GUncertain significance
Select item 2440581	NM_177559.3(CSNK2A1):c.366+9T>C	CSNK2A1	Single nucleotide variant (intron variant)	Okur-Chung neurodevelopmental syndrome	GUncertain significance
Select item 2440585	NM_177559.3(CSNK2A1):c.102-3C>T	CSNK2A1	Single nucleotide variant (intron variant)	Okur-Chung neurodevelopmental syndrome	GUncertain significance

ClinVar