ClinVar Miner

List of variants in gene OPA1 reported as likely benign by Invitae

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Total variants: 33
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HGVS dbSNP
NM_001354663.2(OPA1):c.-260_-243del rs863224140
NM_015560.2(OPA1):c.1089A>T (p.Ile363=) rs1577240973
NM_015560.2(OPA1):c.1137T>G (p.Pro379=) rs139861334
NM_015560.2(OPA1):c.1146A>G (p.Ile382Met) rs143319805
NM_015560.2(OPA1):c.1705+17A>G rs749368763
NM_015560.2(OPA1):c.1771-9A>G rs367798637
NM_015560.2(OPA1):c.2007A>G (p.Ala669=) rs1577287619
NM_015560.2(OPA1):c.2220A>G (p.Gln740=) rs772177326
NM_015560.2(OPA1):c.2256G>T (p.Leu752=) rs148047706
NM_015560.2(OPA1):c.2275+7G>A rs1460816557
NM_015560.2(OPA1):c.239A>G (p.Tyr80Cys) rs151103940
NM_015560.2(OPA1):c.2454G>A (p.Arg818=) rs1577319844
NM_015560.2(OPA1):c.253C>T (p.Arg85Cys) rs372435892
NM_015560.2(OPA1):c.2595G>A (p.Arg865=) rs1192362976
NM_015560.2(OPA1):c.339C>T (p.Tyr113=) rs779836454
NM_015560.2(OPA1):c.556+534G>A rs535724954
NM_015560.2(OPA1):c.625-5443A>G rs375963561
NM_015560.2(OPA1):c.625-5484A>T rs1407152640
NM_015560.2(OPA1):c.625-5514C>A rs764955203
NM_015560.2(OPA1):c.70A>G (p.Ile24Val) rs201520438
NM_015560.2(OPA1):c.85C>G (p.Pro29Ala) rs145565705
NM_015560.2(OPA1):c.88C>T (p.Leu30=) rs185976555
NM_015560.2(OPA1):c.933T>C (p.Ala311=) rs779030198
NM_130837.3(OPA1):c.1149+12G>A
NM_130837.3(OPA1):c.1149+15C>T
NM_130837.3(OPA1):c.1293C>T (p.Thr431=)
NM_130837.3(OPA1):c.1306-10T>C
NM_130837.3(OPA1):c.1719T>C (p.Tyr573=)
NM_130837.3(OPA1):c.1935+18G>A
NM_130837.3(OPA1):c.1936-13_1936-12del
NM_130837.3(OPA1):c.246C>T (p.Tyr82=)
NM_130837.3(OPA1):c.2577G>A (p.Glu859=)
NM_130837.3(OPA1):c.844-20C>A

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