List of variants in gene CSNK2A1 reported as uncertain significance for Okur-Chung neurodevelopmental syndrome

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_177559.3(CSNK2A1):c.62G>A (p.Arg21Gln)	rs1402734448	0.00001
NM_177559.3(CSNK2A1):c.102-3C>T
NM_177559.3(CSNK2A1):c.102-7T>A
NM_177559.3(CSNK2A1):c.1066T>A (p.Ser356Thr)	rs2018014572
NM_177559.3(CSNK2A1):c.1088C>A (p.Pro363His)	rs1193280723
NM_177559.3(CSNK2A1):c.1145C>T (p.Pro382Leu)	rs1064796883
NM_177559.3(CSNK2A1):c.137G>T (p.Gly46Val)	rs2122559628
NM_177559.3(CSNK2A1):c.366+9T>C
NM_177559.3(CSNK2A1):c.385A>G (p.Thr129Ala)
NM_177559.3(CSNK2A1):c.458T>G (p.Met153Arg)	rs2122532009
NM_177559.3(CSNK2A1):c.472A>G (p.Lys158Glu)	rs2018334971
NM_177559.3(CSNK2A1):c.476C>A (p.Pro159His)	rs2122531965
NM_177559.3(CSNK2A1):c.584G>A (p.Arg195Gln)
NM_177559.3(CSNK2A1):c.809A>G (p.Asn270Ser)
NM_177559.3(CSNK2A1):c.955A>G (p.Met319Val)

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