ClinVar Miner

List of variants in gene PEX5 reported as pathogenic for Zellweger spectrum disorders

Included ClinVar conditions (47):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001351132.2(PEX5):c.1279C>T (p.Arg427Ter) rs61752137 0.00003
NM_001351132.2(PEX5):c.1255C>T (p.Gln419Ter) rs1300934931 0.00001
NM_001351132.2(PEX5):c.1258C>T (p.Arg420Ter) rs777735499 0.00001
NM_001351132.2(PEX5):c.583C>T (p.Gln195Ter) rs890363450 0.00001
NM_001351132.2(PEX5):c.709C>T (p.Arg237Ter) rs777733574 0.00001
NM_001351132.2(PEX5):c.119G>A (p.Trp40Ter) rs2135879026
NM_001351132.2(PEX5):c.1264dup (p.Ala422fs) rs1374334296
NM_001351132.2(PEX5):c.1279dup (p.Arg427fs)
NM_001351132.2(PEX5):c.1319_1320del (p.Val440fs)
NM_001351132.2(PEX5):c.1355_1356del (p.Leu452fs)
NM_001351132.2(PEX5):c.1368_1369insGG (p.Arg457fs)
NM_001351132.2(PEX5):c.1426del (p.Leu476fs)
NM_001351132.2(PEX5):c.1469_1470insAC (p.Gln491fs) rs2136243209
NM_001351132.2(PEX5):c.1512T>G (p.Tyr504Ter)
NM_001351132.2(PEX5):c.1521_1527del (p.Val508fs) rs1731078730
NM_001351132.2(PEX5):c.1574G>A (p.Trp525Ter) rs2136254746
NM_001351132.2(PEX5):c.1578T>A (p.Asn526Lys)
NM_001351132.2(PEX5):c.1578T>G (p.Asn526Lys) rs61752138
NM_001351132.2(PEX5):c.1607del (p.Asn536fs)
NM_001351132.2(PEX5):c.30del (p.Glu10fs)
NM_001351132.2(PEX5):c.358C>T (p.Gln120Ter) rs1941140792
NM_001351132.2(PEX5):c.361G>T (p.Glu121Ter) rs1565673352
NM_001351132.2(PEX5):c.416_419del (p.Asp139fs)
NM_001351132.2(PEX5):c.472del (p.Arg158fs) rs2136074154
NM_001351132.2(PEX5):c.478del (p.Ala160fs)
NM_001351132.2(PEX5):c.500C>G (p.Ser167Ter)
NM_001351132.2(PEX5):c.531_534dup (p.Thr179fs) rs2136075415
NM_001351132.2(PEX5):c.54_69dup (p.Phe24fs)
NM_001351132.2(PEX5):c.552G>A (p.Trp184Ter) rs1419213790
NM_001351132.2(PEX5):c.555T>A (p.Tyr185Ter)
NM_001351132.2(PEX5):c.670G>T (p.Glu224Ter)
NM_001351132.2(PEX5):c.674_695dup (p.Ser235fs) rs2136151586
NM_001351132.2(PEX5):c.715C>T (p.Gln239Ter)
NM_001351132.2(PEX5):c.737_738del (p.Glu246fs)
NM_001351132.2(PEX5):c.740_743del (p.Phe247fs)
NM_001351132.2(PEX5):c.76C>T (p.Gln26Ter)
NM_001351132.2(PEX5):c.808dup (p.Leu270fs) rs2136158689
NM_001351132.2(PEX5):c.826C>T (p.Arg276Ter)
NM_001351132.2(PEX5):c.82_83insT (p.Lys28fs)
NM_001351132.2(PEX5):c.88del (p.Leu30fs)
NM_001351132.2(PEX5):c.944_945dup (p.Thr316fs)

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