ClinVar Miner

List of variants in gene OPA1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 91
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HGVS dbSNP
NM_001354663.2(OPA1):c.-260_-243del rs863224140
NM_015560.2(OPA1):c.*6-13T>C rs1243357575
NM_015560.2(OPA1):c.-10C>T rs775614028
NM_015560.2(OPA1):c.-11C>G rs568049951
NM_015560.2(OPA1):c.1066-53T>G rs2306720
NM_015560.2(OPA1):c.1071A>G (p.Ala357=) rs150807064
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.1212+10T>C rs200114656
NM_015560.2(OPA1):c.1212+38A>T rs145646386
NM_015560.2(OPA1):c.1212+9A>G rs759086025
NM_015560.2(OPA1):c.1213-25G>C rs148392527
NM_015560.2(OPA1):c.1242A>C (p.Thr414=) rs1553877924
NM_015560.2(OPA1):c.1300C>T (p.Leu434=) rs1577243073
NM_015560.2(OPA1):c.1313-141G>A rs112831553
NM_015560.2(OPA1):c.1572G>C (p.Gln524His) rs538099724
NM_015560.2(OPA1):c.1705+17A>G rs749368763
NM_015560.2(OPA1):c.1706-19A>C rs1057522968
NM_015560.2(OPA1):c.1771-21_1771-18del rs765277368
NM_015560.2(OPA1):c.1771-9A>G rs367798637
NM_015560.2(OPA1):c.182A>G (p.Gln61Arg) rs558532319
NM_015560.2(OPA1):c.1847+7A>G rs767488490
NM_015560.2(OPA1):c.1863A>G (p.Gln621=) rs773826671
NM_015560.2(OPA1):c.1884A>G (p.Val628=) rs73069703
NM_015560.2(OPA1):c.1923G>A (p.Ala641=) rs138114609
NM_015560.2(OPA1):c.2007A>G (p.Ala669=) rs1577287619
NM_015560.2(OPA1):c.205C>G (p.Pro69Ala) rs750775588
NM_015560.2(OPA1):c.2064G>A (p.Pro688=) rs768448865
NM_015560.2(OPA1):c.2166+10T>C rs371096629
NM_015560.2(OPA1):c.2166+115G>T rs150732301
NM_015560.2(OPA1):c.2167-19C>A rs77355463
NM_015560.2(OPA1):c.2167-265T>G rs12635939
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.2276-134G>C rs375372517
NM_015560.2(OPA1):c.2276-13T>A rs773828534
NM_015560.2(OPA1):c.2276-4dup rs761286590
NM_015560.2(OPA1):c.2341C>T (p.Arg781Trp) rs190235251
NM_015560.2(OPA1):c.2355+13A>G rs371943802
NM_015560.2(OPA1):c.2355+4G>A rs1577307342
NM_015560.2(OPA1):c.239A>G (p.Tyr80Cys) rs151103940
NM_015560.2(OPA1):c.2427T>C (p.Leu809=) rs145999595
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.2614-149T>C rs74450886
NM_015560.2(OPA1):c.2647A>G (p.Ile883Val) rs149866497
NM_015560.2(OPA1):c.2707+15G>C rs199763700
NM_015560.2(OPA1):c.2715A>G (p.Arg905=) rs144898877
NM_015560.2(OPA1):c.2796C>T (p.Arg932=) rs35540805
NM_015560.2(OPA1):c.2808G>C (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.32+14C>T rs201927764
NM_015560.2(OPA1):c.339C>T (p.Tyr113=) rs779836454
NM_015560.2(OPA1):c.530G>T (p.Ser177Ile) rs150279202
NM_015560.2(OPA1):c.534A>G (p.Leu178=) rs758901451
NM_015560.2(OPA1):c.544T>C (p.Phe182Leu) rs769335936
NM_015560.2(OPA1):c.556+534G>A rs535724954
NM_015560.2(OPA1):c.565G>A (p.Glu189Lys) rs569675223
NM_015560.2(OPA1):c.599C>T (p.Ser200Phe) rs200243596
NM_015560.2(OPA1):c.624+235T>C rs73067661
NM_015560.2(OPA1):c.625-4T>A rs374509936
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.625-5527G>T rs373326620
NM_015560.2(OPA1):c.679-279G>A rs3736197
NM_015560.2(OPA1):c.679-4G>A rs377043223
NM_015560.2(OPA1):c.70A>G (p.Ile24Val) rs201520438
NM_015560.2(OPA1):c.756C>T (p.Asp252=) rs147242797
NM_015560.2(OPA1):c.784-11A>C rs376681712
NM_015560.2(OPA1):c.784-12_784-11insTA rs544490050
NM_015560.2(OPA1):c.852G>A (p.Thr284=) rs758922394
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.1286G>A (p.Gly429Asp)
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.2924A>G (p.Asp975Gly)
NM_130837.3(OPA1):c.617C>T (p.Pro206Leu)
NM_130837.3(OPA1):c.844-20C>A
NM_130837.3(OPA1):c.87A>G (p.Pro29=)

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