ClinVar Miner

List of variants in gene POLE2 reported as benign for not provided

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002692.4(POLE2):c.612C>A (p.Val204=) rs3218791 0.26245
NM_002692.4(POLE2):c.1133+15G>A rs3212323 0.22847
NM_002692.4(POLE2):c.564G>A (p.Thr188=) rs34281321 0.02096
NM_002692.4(POLE2):c.170-6T>C rs145475615 0.01129
NM_002692.4(POLE2):c.567G>A (p.Gln189=) rs3218798 0.01004
NM_002692.4(POLE2):c.251A>C (p.His84Pro) rs34857719 0.00756
NM_002692.4(POLE2):c.1497+17T>C rs140187493 0.00454
NM_002692.4(POLE2):c.35C>T (p.Ser12Phe) rs199837996 0.00388
NM_002692.4(POLE2):c.1414T>C (p.Tyr472His) rs34000915 0.00338
NM_002692.4(POLE2):c.1366C>G (p.Leu456Val) rs34574266 0.00325
NM_002692.4(POLE2):c.1043T>C (p.Ile348Thr) rs143942881 0.00248
NM_002692.4(POLE2):c.477C>T (p.Ser159=) rs139370609 0.00210
NM_002692.4(POLE2):c.1068C>G (p.His356Gln) rs139001771 0.00086
NM_002692.4(POLE2):c.576+10T>C rs139611967 0.00085
NM_002692.4(POLE2):c.1053A>G (p.Glu351=) rs149410998 0.00077
NM_002692.4(POLE2):c.1533T>G (p.Val511=) rs149157567 0.00065
NM_002692.4(POLE2):c.16C>T (p.Leu6=) rs375613405 0.00033
NM_002692.4(POLE2):c.1498-6C>T rs146086240 0.00006
NM_002692.4(POLE2):c.682+12T>C rs543143587 0.00001
NM_002692.4(POLE2):c.1566-11dup rs753705907
NM_002692.4(POLE2):c.576+15A>G rs3218797
NM_002692.4(POLE2):c.928+18del
NM_002692.4(POLE2):c.928+18dup

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