ClinVar Miner

List of variants in gene PEX10 reported by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_002617.4(PEX10):c.820A>G (p.Thr274Ala) rs34154371 0.01899
NM_002617.4(PEX10):c.6C>G (p.Ala2=) rs112471479 0.00523
NM_002617.4(PEX10):c.712G>C (p.Gly238Arg) rs61736380 0.00172
NM_002617.4(PEX10):c.495C>T (p.Phe165=) rs150344828 0.00145
NM_002617.4(PEX10):c.601-27A>G rs144264865 0.00103
NM_002617.4(PEX10):c.896C>T (p.Ala299Val) rs78620392 0.00058
NM_002617.4(PEX10):c.*10C>T rs367845280 0.00052
NM_002617.4(PEX10):c.418G>C (p.Gly140Arg) rs76530653 0.00045
NM_002617.4(PEX10):c.627G>A (p.Glu209=) rs141430704 0.00043
NM_002617.4(PEX10):c.816G>T (p.Leu272=) rs144440263 0.00040
NM_002617.4(PEX10):c.765G>A (p.Leu255=) rs140133667 0.00035
NM_002617.4(PEX10):c.812C>T (p.Pro271Leu) rs142088776 0.00034
NM_002617.4(PEX10):c.316C>T (p.Leu106=) rs140340426 0.00029
NM_002617.4(PEX10):c.116C>T (p.Ala39Val) rs149421567 0.00024
NM_002617.4(PEX10):c.611G>A (p.Arg204His) rs199934621 0.00022
NM_002617.4(PEX10):c.220G>A (p.Val74Ile) rs768438726 0.00019
NM_002617.4(PEX10):c.424C>T (p.Arg142Trp) rs372914003 0.00016
NM_002617.4(PEX10):c.423G>A (p.Ala141=) rs138171306 0.00014
NM_002617.4(PEX10):c.425G>A (p.Arg142Gln) rs138843050 0.00014
NM_002617.4(PEX10):c.967C>T (p.Arg323Trp) rs148903253 0.00014
NM_002617.4(PEX10):c.268C>T (p.Leu90=) rs775772867 0.00011
NM_002617.4(PEX10):c.583C>T (p.Leu195Phe) rs116354317 0.00011
NM_002617.4(PEX10):c.915G>A (p.Ala305=) rs374891812 0.00011
NM_002617.4(PEX10):c.427C>T (p.Arg143Cys) rs199667764 0.00009
NM_002617.4(PEX10):c.*7G>T rs760288494 0.00008
NM_002617.4(PEX10):c.704dup (p.Leu236fs) rs61750435 0.00008
NM_002617.4(PEX10):c.78G>A (p.Arg26=) rs987035031 0.00008
NM_002617.4(PEX10):c.527G>A (p.Arg176Gln) rs184150138 0.00007
NM_002617.4(PEX10):c.555C>T (p.His185=) rs75377471 0.00006
NM_002617.4(PEX10):c.605G>A (p.Arg202His) rs371979619 0.00006
NM_002617.4(PEX10):c.814_815del (p.Leu272fs) rs61752093 0.00006
NM_002617.4(PEX10):c.839G>A (p.Arg280His) rs758678654 0.00006
NM_002617.4(PEX10):c.247C>T (p.Arg83Trp) rs377135853 0.00004
NM_002617.4(PEX10):c.271C>T (p.Arg91Cys) rs747921371 0.00004
NM_002617.4(PEX10):c.601-55G>A rs751098874 0.00004
NM_002617.4(PEX10):c.363C>T (p.Pro121=) rs543982780 0.00003
NM_002617.4(PEX10):c.446C>T (p.Thr149Met) rs764948458 0.00003
NM_002617.4(PEX10):c.641G>A (p.Arg214His) rs368143757 0.00003
NM_002617.4(PEX10):c.652_657dup (p.Arg218_Leu219dup) rs1432526114 0.00003
NM_002617.4(PEX10):c.758G>A (p.Arg253His) rs750769868 0.00003
NM_002617.4(PEX10):c.773G>A (p.Arg258His) rs773147980 0.00003
NM_002617.4(PEX10):c.932G>A (p.Arg311Gln) rs724160001 0.00003
NM_002617.4(PEX10):c.484C>T (p.Arg162Trp) rs570706924 0.00002
NM_002617.4(PEX10):c.194-5C>T rs375032738 0.00001
NM_002617.4(PEX10):c.266C>T (p.Ser89Leu) rs769847524 0.00001
NM_002617.4(PEX10):c.668T>C (p.Ile223Thr) rs780850148 0.00001
NM_002617.4(PEX10):c.731G>C (p.Arg244Pro) rs149877113 0.00001
NM_002617.4(PEX10):c.811C>A (p.Pro271Thr) rs886043542 0.00001
NM_002617.4(PEX10):c.838C>T (p.Arg280Cys) rs750424221 0.00001
NM_002617.4(PEX10):c.913-3C>T rs777570617 0.00001
NM_002617.4(PEX10):c.-3G>A rs749847706
NM_002617.4(PEX10):c.266C>G (p.Ser89Trp) rs769847524
NM_002617.4(PEX10):c.274C>T (p.Arg92Cys) rs1214996893
NM_002617.4(PEX10):c.290_291inv (p.Thr97Met)
NM_002617.4(PEX10):c.295del (p.His99fs) rs1557910651
NM_002617.4(PEX10):c.333C>T (p.Leu111=) rs781710848
NM_002617.4(PEX10):c.348G>A (p.Glu116=) rs1553232160
NM_002617.4(PEX10):c.378C>T (p.Pro126=) rs762783424
NM_002617.4(PEX10):c.506A>G (p.Gln169Arg) rs776308498
NM_002617.4(PEX10):c.633G>C (p.Leu211=) rs1442790649
NM_002617.4(PEX10):c.740A>G (p.Lys247Arg) rs1553231833
NM_002617.4(PEX10):c.757C>T (p.Arg253Cys) rs756537855
NM_002617.4(PEX10):c.761del (p.Gly254fs) rs1553231820
NM_002617.4(PEX10):c.835G>T (p.Glu279Ter) rs62641225
NM_002617.4(PEX10):c.867_868insG (p.His290fs) rs797044762
NM_002617.4(PEX10):c.934G>A (p.Glu312Lys) rs886043985

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