ClinVar Miner

List of variants in gene PEX26 reported as uncertain significance for Zellweger syndrome

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_017929.5(PEX26):c.*112C>T rs761715161
NM_017929.5(PEX26):c.*1136G>A rs886057251
NM_017929.5(PEX26):c.*113G>A rs199653646
NM_017929.5(PEX26):c.*114C>T rs45500699
NM_017929.5(PEX26):c.*1152G>C rs886057252
NM_017929.5(PEX26):c.*1171G>A rs184116244
NM_017929.5(PEX26):c.*1194G>A rs118188952
NM_017929.5(PEX26):c.*133C>T rs200243782
NM_017929.5(PEX26):c.*1631G>T rs886057254
NM_017929.5(PEX26):c.*1643_*1646dupGTTT rs375436648
NM_017929.5(PEX26):c.*1684T>C rs886057255
NM_017929.5(PEX26):c.*1720G>A rs749348676
NM_017929.5(PEX26):c.*1740C>G rs139987168
NM_017929.5(PEX26):c.*2070delG rs886057256
NM_017929.5(PEX26):c.*2155A>G rs773334209
NM_017929.5(PEX26):c.*2162G>A rs45489191
NM_017929.5(PEX26):c.*2285C>T rs886057257
NM_017929.5(PEX26):c.*2311G>T rs74714634
NM_017929.5(PEX26):c.*2386C>G rs148534099
NM_017929.5(PEX26):c.*2449C>T rs140919342
NM_017929.5(PEX26):c.*2452G>C rs886057258
NM_017929.5(PEX26):c.*2479G>A rs537299090
NM_017929.5(PEX26):c.*2647G>A rs886057259
NM_017929.5(PEX26):c.*2724G>C rs58564536
NM_017929.5(PEX26):c.*2768C>T rs886057260
NM_017929.5(PEX26):c.*2799dupG rs751296123
NM_017929.5(PEX26):c.*2807_*2808delTT rs754613851
NM_017929.5(PEX26):c.*280G>A rs188897908
NM_017929.5(PEX26):c.*533A>C rs886057247
NM_017929.5(PEX26):c.*568G>A rs886057248
NM_017929.5(PEX26):c.*611_*612dupGA rs886057249
NM_017929.5(PEX26):c.*812C>T rs886057250
NM_017929.5(PEX26):c.*828C>T rs551641353
NM_017929.5(PEX26):c.*912C>T rs79240512
NM_017929.5(PEX26):c.*925A>G rs115277831
NM_017929.5(PEX26):c.*954T>C rs188986907
NM_017929.5(PEX26):c.*977C>T rs181706274
NM_017929.5(PEX26):c.-127G>A rs752393777
NM_017929.5(PEX26):c.-133C>T rs561094254
NM_017929.5(PEX26):c.-167C>T rs886057244
NM_017929.5(PEX26):c.134T>C (p.Leu45Pro) rs61752132
NM_017929.5(PEX26):c.153C>A (p.Phe51Leu) rs777633990
NM_017929.5(PEX26):c.198C>T (p.Ala66=) rs374290931
NM_017929.5(PEX26):c.200A>G (p.Asn67Ser) rs201884779
NM_017929.5(PEX26):c.207C>T (p.Ala69=) rs375516973
NM_017929.5(PEX26):c.208G>T (p.Val70Leu) rs766581207
NM_017929.5(PEX26):c.230+8C>T rs886057245
NM_017929.5(PEX26):c.571C>T (p.Arg191Trp) rs150451390
NM_017929.5(PEX26):c.625G>T (p.Glu209Ter) rs886057246
NM_017929.5(PEX26):c.643G>A (p.Glu215Lys) rs138232280
NM_017929.5(PEX26):c.710G>A (p.Arg237His)
NM_017929.5(PEX26):c.728C>T (p.Ala243Val) rs149153003
NM_017929.5(PEX26):c.815-13C>T rs139370593
NM_017929.5(PEX26):c.889C>T (p.Arg297Cys) rs780701336

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