List of variants in gene CSNK2B reported as uncertain significance for not provided

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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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001320.7(CSNK2B):c.257G>A (p.Arg86His)	rs372125807	0.00001
NM_001320.7(CSNK2B):c.109A>C (p.Thr37Pro)
NM_001320.7(CSNK2B):c.146C>A (p.Ala49Asp)	rs2151185508
NM_001320.7(CSNK2B):c.203A>T (p.Gln68Leu)	rs2536962697
NM_001320.7(CSNK2B):c.236T>C (p.Leu79Pro)	rs2151187226
NM_001320.7(CSNK2B):c.251A>T (p.His84Leu)
NM_001320.7(CSNK2B):c.277G>A (p.Gly93Ser)	rs2536963048
NM_001320.7(CSNK2B):c.278G>T (p.Gly93Val)	rs2536963059
NM_001320.7(CSNK2B):c.318T>G (p.Phe106Leu)	rs1583610423
NM_001320.7(CSNK2B):c.32C>T (p.Ser11Phe)	rs2536947688
NM_001320.7(CSNK2B):c.340T>C (p.Cys114Arg)	rs1802003420
NM_001320.7(CSNK2B):c.341G>A (p.Cys114Tyr)
NM_001320.7(CSNK2B):c.365T>C (p.Ile122Thr)	rs2536966348
NM_001320.7(CSNK2B):c.419_420delinsTA (p.Cys140Leu)
NM_001320.7(CSNK2B):c.422T>C (p.Met141Thr)	rs1562052640
NM_001320.7(CSNK2B):c.475T>G (p.Phe159Val)	rs2536968107
NM_001320.7(CSNK2B):c.557G>T (p.Arg186Met)	rs2151189059
NM_001320.7(CSNK2B):c.565G>A (p.Gly189Ser)	rs2151189797
NM_001320.7(CSNK2B):c.575T>G (p.Ile192Ser)
NM_001320.7(CSNK2B):c.577del (p.His193fs)	rs1802056827
NM_001320.7(CSNK2B):c.62TCT[1] (p.Phe22del)	rs2151182182
NM_001320.7(CSNK2B):c.631G>A (p.Val211Ile)	rs2151189915
NM_001320.7(CSNK2B):c.647G>C (p.Ter216Ser)
NM_001320.7(CSNK2B):c.68G>T (p.Cys23Phe)	rs1801760887
NM_001320.7(CSNK2B):c.88A>C (p.Ile30Leu)

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