List of variants in gene PEX26 reported by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_001127649.3(PEX26):c.371+108C>T	rs464541	0.72214
NM_001127649.3(PEX26):c.*167G>A	rs464385	0.52045
NC_000022.11:g.18077804C>T	rs462055	0.28421
NM_001127649.3(PEX26):c.371+272G>A	rs17809735	0.07738
NC_000022.11:g.18077845T>G	rs12157958	0.05953
NM_001127649.3(PEX26):c.667+204C>T	rs75620601	0.02729
NM_001127649.3(PEX26):c.231-45T>G	rs114973307	0.01860
NM_001127649.3(PEX26):c.-363G>C	rs138787474	0.01598
NM_017929.5(PEX26):c.-148C>T	rs115617644	0.01576
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.667+264T>C	rs11914004	0.00836
NC_000022.11:g.18077831T>C	rs41277574	0.00722
NM_001127649.3(PEX26):c.130C>T (p.Leu44Phe)	rs150895887	0.00683
NM_001127649.3(PEX26):c.372-177C>T	rs11913286	0.00593
NM_001127649.3(PEX26):c.815-13C>T	rs139370593	0.00381
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.153C>A (p.Phe51Leu)	rs777633990	0.00002
NM_001127649.3(PEX26):c.574C>T (p.Arg192Ter)	rs61752136	0.00001
NM_001127649.3(PEX26):c.230+6T>A	rs2123644704
NM_001127649.3(PEX26):c.34dup (p.Leu12fs)	rs61752129
NM_001127649.3(PEX26):c.353C>G (p.Pro118Arg)	rs61752135
NM_001127649.3(PEX26):c.368T>C (p.Leu123Pro)	rs886039598
NM_001127649.3(PEX26):c.667+1del	rs1556589033
NM_001127649.3(PEX26):c.815-331C>A	rs34301327
NM_001127649.3(PEX26):c.896A>G (p.Tyr299Cys)

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