ClinVar Miner

List of variants in gene CSNK2B reported as uncertain significance

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Total variants: 50
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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.581C>T (p.Pro194Leu) rs1246917499 0.00001
NM_001320.7(CSNK2B):c.109A>C (p.Thr37Pro)
NM_001320.7(CSNK2B):c.116T>C (p.Leu39Pro) rs2151185431
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.229G>A (p.Glu77Lys) rs1583608433
NM_001320.7(CSNK2B):c.236T>C (p.Leu79Pro) rs2151187226
NM_001320.7(CSNK2B):c.238T>A (p.Tyr80Asn) rs1554170318
NM_001320.7(CSNK2B):c.251A>T (p.His84Leu)
NM_001320.7(CSNK2B):c.256C>T (p.Arg86Cys) rs1801961640
NM_001320.7(CSNK2B):c.265del (p.Thr90fs) rs1583608557
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.289A>G (p.Met97Val) rs2536963142
NM_001320.7(CSNK2B):c.291+2T>C
NM_001320.7(CSNK2B):c.318T>G (p.Phe106Leu) rs1583610423
NM_001320.7(CSNK2B):c.323A>G (p.Tyr108Cys)
NM_001320.7(CSNK2B):c.325T>C (p.Cys109Arg) rs2536966124
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.367+6T>C rs2151188436
NM_001320.7(CSNK2B):c.419_420delinsTA (p.Cys140Leu)
NM_001320.7(CSNK2B):c.422T>C (p.Met141Thr) rs1562052640
NM_001320.7(CSNK2B):c.463G>C (p.Asp155His) rs2536968051
NM_001320.7(CSNK2B):c.467G>A (p.Gly156Asp) rs2151188873
NM_001320.7(CSNK2B):c.467_468delinsTT (p.Gly156Val) rs2151188878
NM_001320.7(CSNK2B):c.475T>C (p.Phe159Leu)
NM_001320.7(CSNK2B):c.475T>G (p.Phe159Val) rs2536968107
NM_001320.7(CSNK2B):c.491C>G (p.Pro164Arg) rs2151188947
NM_001320.7(CSNK2B):c.491C>T (p.Pro164Leu) rs2151188947
NM_001320.7(CSNK2B):c.501C>T (p.Leu167=) rs1169432962
NM_001320.7(CSNK2B):c.505A>G (p.Met169Val) rs2536968227
NM_001320.7(CSNK2B):c.50G>A (p.Arg17His)
NM_001320.7(CSNK2B):c.517G>A (p.Glu173Lys)
NM_001320.7(CSNK2B):c.557G>T (p.Arg186Met) rs2151189059
NM_001320.7(CSNK2B):c.558-11C>T rs2536970792
NM_001320.7(CSNK2B):c.565G>A (p.Gly189Ser) rs2151189797
NM_001320.7(CSNK2B):c.566G>T (p.Gly189Val) rs1802055915
NM_001320.7(CSNK2B):c.569T>C (p.Phe190Ser) rs2536970927
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.67T>C (p.Cys23Arg) rs2536947987
NM_001320.7(CSNK2B):c.68G>T (p.Cys23Phe) rs1801760887
NM_001320.7(CSNK2B):c.88A>C (p.Ile30Leu)

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