ClinVar Miner

List of variants in gene CEP152 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001194998.2(CEP152):c.344G>A (p.Arg115Gln) rs188101277 0.00303
NM_001194998.2(CEP152):c.2878T>C (p.Trp960Arg) rs201342438 0.00263
NM_001194998.2(CEP152):c.1180A>G (p.Ile394Val) rs181295720 0.00215
NM_001194998.2(CEP152):c.4072C>G (p.Gln1358Glu) rs149478199 0.00203
NM_001194998.2(CEP152):c.3313C>G (p.Leu1105Val) rs74553953 0.00162
NM_001194998.2(CEP152):c.4784C>T (p.Pro1595Leu) rs145652839 0.00160
NM_001194998.2(CEP152):c.61G>A (p.Glu21Lys) rs187563127 0.00147
NM_001194998.2(CEP152):c.767T>C (p.Ile256Thr) rs201217824 0.00120
NM_001194998.2(CEP152):c.3712C>G (p.Leu1238Val) rs116014437 0.00118
NM_001194998.2(CEP152):c.644G>A (p.Ser215Asn) rs200957146 0.00118
NM_001194998.2(CEP152):c.925A>C (p.Lys309Gln) rs199862615 0.00118
NM_001194998.2(CEP152):c.982A>C (p.Lys328Gln) rs201942310 0.00118
NM_001194998.2(CEP152):c.4077C>G (p.Ser1359Arg) rs114263428 0.00117
NM_001194998.2(CEP152):c.*5G>A rs74012133 0.00096
NM_001194998.2(CEP152):c.2804A>G (p.Gln935Arg) rs74245641 0.00016
NM_001194998.2(CEP152):c.2777A>T (p.Glu926Val) rs117557829 0.00014
NM_001194998.2(CEP152):c.4320T>C (p.His1440=) rs372379014 0.00014
NM_001194998.2(CEP152):c.4175T>C (p.Ile1392Thr) rs186930123 0.00011
NM_001194998.2(CEP152):c.3921C>T (p.Thr1307=) rs777663214 0.00007
NM_001194998.2(CEP152):c.3433C>A (p.Pro1145Thr) rs200055660 0.00006
NM_001194998.2(CEP152):c.3100C>T (p.Arg1034Trp) rs184240876 0.00004
NM_001194998.2(CEP152):c.3729A>G (p.Pro1243=) rs562708873 0.00001
NM_001194998.2(CEP152):c.1377A>T (p.Ala459=)
NM_001194998.2(CEP152):c.1392A>G (p.Ala464=)
NM_001194998.2(CEP152):c.3780G>T (p.Gly1260=) rs199777941
NM_001194998.2(CEP152):c.5112C>T (p.Ser1704=)

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