ClinVar Miner

List of variants in gene PEX26 reported as benign for Peroxisome biogenesis disorder 7A

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Total variants: 28
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HGVS dbSNP
NM_001127649.3(PEX26):c.*1003T>G rs79085553
NM_001127649.3(PEX26):c.*10C>T rs117472525
NM_001127649.3(PEX26):c.*1265T>A rs456551
NM_001127649.3(PEX26):c.*1283C>T rs73876563
NM_001127649.3(PEX26):c.*1590G>A rs5992169
NM_001127649.3(PEX26):c.*1608G>A rs116824049
NM_001127649.3(PEX26):c.*1623G>T rs114698763
NM_001127649.3(PEX26):c.*1635G>C rs361703
NM_001127649.3(PEX26):c.*1669C>G rs112015789
NM_001127649.3(PEX26):c.*167G>A rs464385
NM_001127649.3(PEX26):c.*1778C>T rs79447039
NM_001127649.3(PEX26):c.*1859A>C rs146739242
NM_001127649.3(PEX26):c.*1957G>A rs11913772
NM_001127649.3(PEX26):c.*2051A>G rs361946
NM_001127649.3(PEX26):c.*2281T>C rs362209
NM_001127649.3(PEX26):c.*2701G>C rs114075265
NM_001127649.3(PEX26):c.*2878C>T rs116424707
NM_001127649.3(PEX26):c.*400C>T rs74988725
NM_001127649.3(PEX26):c.*464A>G rs141229564
NM_001127649.3(PEX26):c.*692T>C rs79936154
NM_001127649.3(PEX26):c.*754A>G rs114146293
NM_001127649.3(PEX26):c.*829A>G rs362057
NM_001127649.3(PEX26):c.*917C>T rs9605518
NM_001127649.3(PEX26):c.*943G>A rs79785382
NM_001127649.3(PEX26):c.*944C>A rs78412274
NM_001127649.3(PEX26):c.*987T>C rs361807
NM_001127649.3(PEX26):c.-318A>G rs62239019
NM_001199319.1(PEX26):c.-148C>T rs115617644

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