ClinVar Miner

List of variants in gene CDK13 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_003718.5(CDK13):c.2600+276A>G rs798853 0.96856
NM_003718.5(CDK13):c.2898-254A>G rs798856 0.65609
NM_003718.5(CDK13):c.2354-235A>T rs1522878 0.55932
NM_003718.5(CDK13):c.2543+217A>G rs9639818 0.54345
NM_003718.5(CDK13):c.1871+215G>A rs1257699 0.44860
NM_003718.5(CDK13):c.2183-289T>G rs10253590 0.26788
NM_003718.5(CDK13):c.1211+222G>A rs9655407 0.26766
NM_003718.5(CDK13):c.3688+208G>A rs2077124 0.26686
NM_003718.5(CDK13):c.2543+141C>T rs9639817 0.26616
NM_003718.5(CDK13):c.2781-240A>G rs10232399 0.19785
NM_003718.5(CDK13):c.2043-253T>C rs10241835 0.15426
NM_003718.5(CDK13):c.*99A>G rs17538328 0.11063
NM_003718.5(CDK13):c.3689-166A>G rs2015842 0.09018
NM_003718.5(CDK13):c.1498A>G (p.Thr500Ala) rs3735135 0.08199
NM_003718.5(CDK13):c.3072G>A (p.Lys1024=) rs2302341 0.08147
NM_003718.5(CDK13):c.3236-217A>G rs12669872 0.08136
NM_003718.5(CDK13):c.3939T>C (p.Asp1313=) rs17496805 0.03439
NM_003718.5(CDK13):c.2043-210A>C rs17496331 0.03399
NM_003718.5(CDK13):c.2353+172G>A rs17496388 0.02682
NM_003718.5(CDK13):c.2182+146A>G rs79353776 0.01950
NM_003718.5(CDK13):c.3689-194del rs5883719

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