ClinVar Miner

List of variants in gene PLK4 reported as benign for not provided

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_014264.5(PLK4):c.126+78G>A rs3811741 0.74342
NM_014264.5(PLK4):c.694T>A (p.Ser232Thr) rs3811740 0.71105
NM_014264.5(PLK4):c.338-273C>T rs111785587 0.04364
NM_014264.5(PLK4):c.126+222A>G rs111383611 0.03723
NM_014264.5(PLK4):c.2189-36G>A rs72616963 0.02732
NM_014264.5(PLK4):c.2703+12C>G rs17012743 0.02716
NM_014264.5(PLK4):c.2563-139T>A rs60279389 0.02710
NM_014264.5(PLK4):c.2241G>A (p.Gly747=) rs56250604 0.02703
NM_014264.5(PLK4):c.2039-254G>T rs116020281 0.02563
NM_014264.5(PLK4):c.2563-56A>G rs41278097 0.02459
NM_014264.5(PLK4):c.2835A>G (p.Pro945=) rs41278099 0.01765
NM_014264.5(PLK4):c.2556T>C (p.Asn852=) rs13129689 0.01216
NM_014264.5(PLK4):c.1556G>C (p.Trp519Ser) rs56043017 0.00721
NM_014264.5(PLK4):c.2188+16A>G rs142628767 0.00564
NM_014264.5(PLK4):c.2483C>T (p.Thr828Met) rs61735390 0.00513
NM_014264.5(PLK4):c.1428A>T (p.Val476=) rs112831813 0.00392
NM_014264.5(PLK4):c.2895G>A (p.Pro965=) rs6820138 0.00338
NM_014264.5(PLK4):c.1020A>C (p.Gly340=) rs7664937 0.00316
NM_014264.5(PLK4):c.2109C>A (p.Ile703=) rs74770705 0.00271
NM_014264.5(PLK4):c.2704-19A>T rs11933723 0.00242
NM_014264.5(PLK4):c.2433T>C (p.Ser811=) rs146056387 0.00195
NM_014264.5(PLK4):c.1359-18T>G rs199791103 0.00157
NM_014264.5(PLK4):c.1830+7C>G rs367752526 0.00061
NM_014264.5(PLK4):c.1364A>G (p.Asn455Ser) rs373379984 0.00019
NM_014264.5(PLK4):c.127-258del rs5861839
NM_014264.5(PLK4):c.1359-11del rs576645805
NM_014264.5(PLK4):c.2039-7dup rs753429702
NM_014264.5(PLK4):c.2184T>C (p.Tyr728=)
NM_014264.5(PLK4):c.2189-3del rs57995643
NM_014264.5(PLK4):c.2189-3dup rs57995643
NM_014264.5(PLK4):c.2490G>T (p.Glu830Asp) rs17012739
NM_014264.5(PLK4):c.337+20del rs764441801
NM_014264.5(PLK4):c.337+20dup
NM_014264.5(PLK4):c.338-14del rs750472455

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