ClinVar Miner

List of variants in gene PEX26 reported as likely benign for Zellweger syndrome

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_001127649.3(PEX26):c.*114C>T rs45500699
NM_001127649.3(PEX26):c.*1740C>G rs139987168
NM_001127649.3(PEX26):c.*2162G>A rs45489191
NM_001127649.3(PEX26):c.*2311G>T rs74714634
NM_001127649.3(PEX26):c.*2703G>A
NM_001127649.3(PEX26):c.*279G>A
NM_001127649.3(PEX26):c.*566T>C
NM_001127649.3(PEX26):c.*925A>G rs115277831
NM_001127649.3(PEX26):c.-363G>C rs138787474
NM_001127649.3(PEX26):c.130C>T (p.Leu44Phe) rs150895887
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.318C>G (p.Val106=) rs142072315
NM_001127649.3(PEX26):c.409G>C (p.Val137Leu) rs142648687
NM_001127649.3(PEX26):c.441C>T (p.Asp147=) rs770611373
NM_001127649.3(PEX26):c.457C>G (p.Leu153Val) rs12484657
NM_001127649.3(PEX26):c.667+8A>G rs200880379
NM_001127649.3(PEX26):c.815-13C>T rs139370593
NM_001127649.3(PEX26):c.911G>A (p.Arg304His) rs17851387

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