ClinVar Miner

List of variants in gene PEX26 reported by Eurofins NTD LLC (GA)

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Total variants: 56
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HGVS dbSNP gnomAD frequency
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.130C>T (p.Leu44Phe) rs150895887 0.00683
NM_001127649.3(PEX26):c.325T>C (p.Tyr109His) rs45567240 0.00190
NM_001127649.3(PEX26):c.200A>G (p.Asn67Ser) rs201884779 0.00179
NM_001127649.3(PEX26):c.409G>C (p.Val137Leu) rs142648687 0.00179
NM_001127649.3(PEX26):c.911G>A (p.Arg304His) rs17851387 0.00121
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.667+8A>G rs200880379 0.00046
NM_001127649.3(PEX26):c.895dup (p.Tyr299fs) rs759821636 0.00036
NM_001127649.3(PEX26):c.318C>G (p.Val106=) rs142072315 0.00027
NM_001127649.3(PEX26):c.198C>T (p.Ala66=) rs374290931 0.00026
NM_001127649.3(PEX26):c.207C>T (p.Ala69=) rs375516973 0.00026
NM_001127649.3(PEX26):c.716T>C (p.Leu239Pro) rs757411841 0.00018
NM_001127649.3(PEX26):c.882A>G (p.Ala294=) rs751507771 0.00015
NM_001127649.3(PEX26):c.668-5G>T rs767742108 0.00012
NM_001127649.3(PEX26):c.571C>T (p.Arg191Trp) rs150451390 0.00011
NM_001127649.3(PEX26):c.98C>T (p.Pro33Leu) rs368118099 0.00010
NM_001127649.3(PEX26):c.33C>G (p.Pro11=) rs199668827 0.00009
NM_001127649.3(PEX26):c.886T>C (p.Ser296Pro) rs143243841 0.00009
NM_001127649.3(PEX26):c.292C>T (p.Arg98Trp) rs62641228 0.00008
NM_001127649.3(PEX26):c.29C>T (p.Ala10Val) rs768425084 0.00006
NM_001127649.3(PEX26):c.441C>T (p.Asp147=) rs770611373 0.00006
NM_001127649.3(PEX26):c.496C>T (p.Arg166Trp) rs369695924 0.00006
NM_001127649.3(PEX26):c.32C>T (p.Pro11Leu) rs200279475 0.00004
NM_001127649.3(PEX26):c.786C>G (p.Leu262=) rs759864013 0.00004
NM_001127649.3(PEX26):c.725C>T (p.Ser242Phe) rs779828574 0.00003
NM_001127649.3(PEX26):c.120G>C (p.Glu40Asp) rs1010208134 0.00002
NM_001127649.3(PEX26):c.153C>A (p.Phe51Leu) rs777633990 0.00002
NM_001127649.3(PEX26):c.230+3A>G rs757200331 0.00002
NM_001127649.3(PEX26):c.38G>T (p.Arg13Met) rs1419370284 0.00002
NM_001127649.3(PEX26):c.461C>T (p.Pro154Leu) rs998546145 0.00002
NM_001127649.3(PEX26):c.558C>T (p.Ala186=) rs372621690 0.00002
NM_001127649.3(PEX26):c.863G>A (p.Arg288His) rs370622812 0.00002
NM_001127649.3(PEX26):c.243G>T (p.Val81=) rs772417180 0.00001
NM_001127649.3(PEX26):c.48G>T (p.Gly16=) rs764244307 0.00001
NM_001127649.3(PEX26):c.540A>G (p.Leu180=) rs374381444 0.00001
NM_001127649.3(PEX26):c.554C>T (p.Ala185Val) rs370147115 0.00001
NM_001127649.3(PEX26):c.628C>T (p.His210Tyr) rs1199052809 0.00001
NM_001127649.3(PEX26):c.662T>G (p.Leu221Arg) rs767345970 0.00001
NM_001127649.3(PEX26):c.669C>A (p.Gly223=) rs398124339 0.00001
NM_001127649.3(PEX26):c.71C>G (p.Pro24Arg) rs771847925 0.00001
NM_001127649.3(PEX26):c.815-10T>G rs794727805 0.00001
NM_001127649.3(PEX26):c.817T>G (p.Ser273Ala) rs745490062 0.00001
NM_001127649.3(PEX26):c.854A>G (p.Gln285Arg) rs767603690 0.00001
NM_001127649.3(PEX26):c.119A>C (p.Glu40Ala) rs1158271855
NM_001127649.3(PEX26):c.324G>A (p.Gln108=) rs1569186417
NM_001127649.3(PEX26):c.34dup (p.Leu12fs) rs61752129
NM_001127649.3(PEX26):c.372-5T>G rs1569187768
NM_001127649.3(PEX26):c.423G>A (p.Val141=) rs749533743
NM_001127649.3(PEX26):c.662T>A (p.Leu221Gln) rs767345970
NM_001127649.3(PEX26):c.795G>A (p.Leu265=) rs904472324
NM_001127649.3(PEX26):c.815-6C>T rs1556590594
NM_001127649.3(PEX26):c.99G>C (p.Pro33=) rs1284941471

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