ClinVar Miner

List of variants reported as uncertain significance for Peroxisome biogenesis disorder 7A

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Total variants: 83
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HGVS dbSNP
NC_000022.11:g.18077922T>C rs0
NC_000022.11:g.18077926G>A rs0
NC_000022.11:g.18077965G>T rs0
NM_001127649.3(PEX26):c.*112C>T rs761715161
NM_001127649.3(PEX26):c.*1136G>A rs886057251
NM_001127649.3(PEX26):c.*113G>A rs199653646
NM_001127649.3(PEX26):c.*1152G>C rs886057252
NM_001127649.3(PEX26):c.*1156T>C rs0
NM_001127649.3(PEX26):c.*1171G>A rs184116244
NM_001127649.3(PEX26):c.*1194G>A rs118188952
NM_001127649.3(PEX26):c.*122A>C rs0
NM_001127649.3(PEX26):c.*133C>T rs200243782
NM_001127649.3(PEX26):c.*1488T>C rs0
NM_001127649.3(PEX26):c.*1493C>G rs0
NM_001127649.3(PEX26):c.*1509C>G rs0
NM_001127649.3(PEX26):c.*1618G>C rs0
NM_001127649.3(PEX26):c.*1627G>T rs0
NM_001127649.3(PEX26):c.*1631G>T rs886057254
NM_001127649.3(PEX26):c.*1639G>T rs0
NM_001127649.3(PEX26):c.*1684T>C rs886057255
NM_001127649.3(PEX26):c.*1720G>A rs749348676
NM_001127649.3(PEX26):c.*1922C>T rs0
NM_001127649.3(PEX26):c.*1928A>C rs0
NM_001127649.3(PEX26):c.*1957G>T rs0
NM_001127649.3(PEX26):c.*2155A>G rs773334209
NM_001127649.3(PEX26):c.*2195A>G rs0
NM_001127649.3(PEX26):c.*2282G>A rs0
NM_001127649.3(PEX26):c.*2285C>T rs886057257
NM_001127649.3(PEX26):c.*2308A>T rs0
NM_001127649.3(PEX26):c.*2339G>A rs0
NM_001127649.3(PEX26):c.*2369C>G rs0
NM_001127649.3(PEX26):c.*2370T>A rs0
NM_001127649.3(PEX26):c.*2386C>G rs148534099
NM_001127649.3(PEX26):c.*2449C>T rs140919342
NM_001127649.3(PEX26):c.*2452G>C rs886057258
NM_001127649.3(PEX26):c.*2479G>A rs537299090
NM_001127649.3(PEX26):c.*2523C>T rs0
NM_001127649.3(PEX26):c.*2604G>C rs0
NM_001127649.3(PEX26):c.*2647G>A rs886057259
NM_001127649.3(PEX26):c.*2651C>T rs0
NM_001127649.3(PEX26):c.*2724G>C rs58564536
NM_001127649.3(PEX26):c.*2768C>T rs886057260
NM_001127649.3(PEX26):c.*280G>A rs188897908
NM_001127649.3(PEX26):c.*2810G>C rs0
NM_001127649.3(PEX26):c.*2904T>C rs0
NM_001127649.3(PEX26):c.*36G>A rs0
NM_001127649.3(PEX26):c.*439C>G rs0
NM_001127649.3(PEX26):c.*533A>C rs886057247
NM_001127649.3(PEX26):c.*568G>A rs886057248
NM_001127649.3(PEX26):c.*578A>G rs0
NM_001127649.3(PEX26):c.*662C>T rs0
NM_001127649.3(PEX26):c.*802A>G rs0
NM_001127649.3(PEX26):c.*812C>T rs886057250
NM_001127649.3(PEX26):c.*828C>T rs551641353
NM_001127649.3(PEX26):c.*829A>T rs0
NM_001127649.3(PEX26):c.*954T>C rs188986907
NM_001127649.3(PEX26):c.*977C>T rs181706274
NM_001127649.3(PEX26):c.-375G>A rs752393777
NM_001127649.3(PEX26):c.-381C>T rs561094254
NM_001127649.3(PEX26):c.-80C>T rs0
NM_001127649.3(PEX26):c.134T>C (p.Leu45Pro) rs61752132
NM_001127649.3(PEX26):c.153C>A (p.Phe51Leu) rs777633990
NM_001127649.3(PEX26):c.198C>T (p.Ala66=) rs374290931
NM_001127649.3(PEX26):c.200A>G (p.Asn67Ser) rs201884779
NM_001127649.3(PEX26):c.207C>T (p.Ala69=) rs375516973
NM_001127649.3(PEX26):c.208G>T (p.Val70Leu) rs766581207
NM_001127649.3(PEX26):c.230+8C>T rs886057245
NM_001127649.3(PEX26):c.29C>T (p.Ala10Val) rs768425084
NM_001127649.3(PEX26):c.325T>C (p.Tyr109His) rs45567240
NM_001127649.3(PEX26):c.32C>T (p.Pro11Leu) rs200279475
NM_001127649.3(PEX26):c.409G>C (p.Val137Leu) rs142648687
NM_001127649.3(PEX26):c.554C>T (p.Ala185Val) rs370147115
NM_001127649.3(PEX26):c.571C>T (p.Arg191Trp) rs150451390
NM_001127649.3(PEX26):c.625G>T (p.Glu209Ter) rs886057246
NM_001127649.3(PEX26):c.643G>A (p.Glu215Lys) rs138232280
NM_001127649.3(PEX26):c.667+8A>G rs200880379
NM_001127649.3(PEX26):c.709C>T (p.Arg237Cys) rs0
NM_001127649.3(PEX26):c.728C>T (p.Ala243Val) rs149153003
NM_001127649.3(PEX26):c.814+15C>T rs0
NM_001127649.3(PEX26):c.889C>T (p.Arg297Cys) rs780701336
NM_001127649.3(PEX26):c.911G>A (p.Arg304His) rs17851387
NM_001127649.3(PEX26):c.98C>T (p.Pro33Leu) rs368118099
NM_001199319.1(PEX26):c.-167C>T rs886057244

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