ClinVar Miner

List of variants in gene PEX26 reported as benign for Zellweger spectrum disorders

Included ClinVar conditions (47):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001127649.3(PEX26):c.*2281T>C rs362209 0.99208
NM_001127649.3(PEX26):c.*2051A>G rs361946 0.88398
NM_001127649.3(PEX26):c.*987T>C rs361807 0.88380
NM_001127649.3(PEX26):c.*1265T>A rs456551 0.52154
NM_001127649.3(PEX26):c.*167G>A rs464385 0.52045
NM_001127649.3(PEX26):c.*1590G>A rs5992169 0.10823
NM_001127649.3(PEX26):c.*1669C>G rs112015789 0.10796
NM_001127649.3(PEX26):c.*917C>T rs9605518 0.10773
NM_001127649.3(PEX26):c.*1635G>C rs361703 0.09478
NM_001127649.3(PEX26):c.*1623G>T rs114698763 0.06369
NM_001127649.3(PEX26):c.*754A>G rs114146293 0.03730
NM_001127649.3(PEX26):c.*2878C>T rs116424707 0.02655
NM_001127649.3(PEX26):c.*1608G>A rs116824049 0.02602
NM_001127649.3(PEX26):c.*1003T>G rs79085553 0.02437
NM_001127649.3(PEX26):c.*2701G>C rs114075265 0.02360
NM_001127649.3(PEX26):c.*400C>T rs74988725 0.01840
NM_001127649.3(PEX26):c.*692T>C rs79936154 0.01840
NM_001127649.3(PEX26):c.*943G>A rs79785382 0.01835
NM_017929.5(PEX26):c.-148C>T rs115617644 0.01576
NM_001127649.3(PEX26):c.*464A>G rs141229564 0.01278
NM_001127649.3(PEX26):c.*10C>T rs117472525 0.01244
NM_001127649.3(PEX26):c.457C>G (p.Leu153Val) rs12484657 0.01096
NM_001127649.3(PEX26):c.*1778C>T rs79447039 0.01095
NM_001127649.3(PEX26):c.*1957G>A rs11913772 0.01094
NM_001127649.3(PEX26):c.130C>T (p.Leu44Phe) rs150895887 0.00683
NM_001127649.3(PEX26):c.815-13C>T rs139370593 0.00381
NM_001127649.3(PEX26):c.325T>C (p.Tyr109His) rs45567240 0.00190
NM_001127649.3(PEX26):c.497G>A (p.Arg166Gln) rs34194489 0.00098
NM_001127649.3(PEX26):c.728C>T (p.Ala243Val) rs149153003 0.00083
NM_001127649.3(PEX26):c.643G>A (p.Glu215Lys) rs138232280 0.00063
NM_001127649.3(PEX26):c.882A>G (p.Ala294=) rs751507771 0.00015
NM_001127649.3(PEX26):c.501G>A (p.Val167=) rs201666490 0.00013
NM_001127649.3(PEX26):c.*1283C>T rs73876563
NM_001127649.3(PEX26):c.*1532_*1535dup rs361782
NM_001127649.3(PEX26):c.*1661_*1662insACTC rs361571
NM_001127649.3(PEX26):c.*1859A>C rs146739242
NM_001127649.3(PEX26):c.*829A>G rs362057
NM_001127649.3(PEX26):c.*944C>A rs78412274
NM_001127649.3(PEX26):c.372-12dup rs1489019658
NM_001127649.3(PEX26):c.814+22del

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