ClinVar Miner

List of variants in gene OPA1 reported as uncertain significance by GeneDx

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Total variants: 34
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HGVS dbSNP
NM_001354663.2(OPA1):c.-260_-243del rs863224140
NM_015560.2(OPA1):c.1003C>T (p.Pro335Ser) rs1057524630
NM_015560.2(OPA1):c.1024A>G (p.Lys342Glu) rs1057517999
NM_015560.2(OPA1):c.1028A>C (p.Asp343Ala) rs756981921
NM_015560.2(OPA1):c.1425T>A (p.Asn475Lys) rs863224137
NM_015560.2(OPA1):c.1535T>C (p.Ile512Thr) rs148834015
NM_015560.2(OPA1):c.1648G>T (p.Asp550Tyr) rs1131691441
NM_015560.2(OPA1):c.1673A>C (p.Glu558Ala) rs949979832
NM_015560.2(OPA1):c.1703A>G (p.Lys568Arg) rs1553879126
NM_015560.2(OPA1):c.1712G>A (p.Arg571His) rs140606054
NM_015560.2(OPA1):c.1841A>T (p.Lys614Ile) rs146601330
NM_015560.2(OPA1):c.1880G>A (p.Arg627Lys) rs772040791
NM_015560.2(OPA1):c.1978T>C (p.Trp660Arg) rs1553881180
NM_015560.2(OPA1):c.212G>A (p.Arg71His) rs766106312
NM_015560.2(OPA1):c.2264G>A (p.Arg755His) rs762258708
NM_015560.2(OPA1):c.22G>T (p.Ala8Ser) rs794726939
NM_015560.2(OPA1):c.2341C>T (p.Arg781Trp) rs190235251
NM_015560.2(OPA1):c.2452C>T (p.Arg818Trp) rs143252541
NM_015560.2(OPA1):c.2471G>A (p.Arg824Gln) rs200412464
NM_015560.2(OPA1):c.2564T>G (p.Leu855Arg) rs139106405
NM_015560.2(OPA1):c.2675A>C (p.Asn892Thr) rs750518068
NM_015560.2(OPA1):c.2720A>G (p.Glu907Gly) rs863224138
NM_015560.2(OPA1):c.272C>G (p.Ala91Gly) rs1085307621
NM_015560.2(OPA1):c.2737G>T (p.Val913Leu) rs863224139
NM_015560.2(OPA1):c.2862A>C (p.Glu954Asp) rs189036094
NM_015560.2(OPA1):c.49T>A (p.Leu17Ile) rs760770105
NM_015560.2(OPA1):c.516T>G (p.Ile172Met) rs863224126
NM_015560.2(OPA1):c.530G>T (p.Ser177Ile) rs150279202
NM_015560.2(OPA1):c.542A>G (p.Asp181Gly) rs138884045
NM_015560.2(OPA1):c.599C>T (p.Ser200Phe) rs200243596
NM_015560.2(OPA1):c.625-5451G>A rs143918255
NM_015560.2(OPA1):c.625-5459G>A rs138350727
NM_015560.2(OPA1):c.625-5487C>G rs1131691832
NM_015560.2(OPA1):c.799A>G (p.Met267Val) rs938874214

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