ClinVar Miner

List of variants in gene OPA1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_015560.2(OPA1):c.*1031A>T rs114606850
NM_015560.2(OPA1):c.*1425G>A rs117826024
NM_015560.2(OPA1):c.*1610C>A rs73069785
NM_015560.2(OPA1):c.*2115G>A rs144079165
NM_015560.2(OPA1):c.*220A>G rs76421015
NM_015560.2(OPA1):c.*2286T>C rs115575058
NM_015560.2(OPA1):c.*2408A>G rs73069788
NM_015560.2(OPA1):c.*2993C>A rs143991575
NM_015560.2(OPA1):c.*3027A>G rs56329083
NM_015560.2(OPA1):c.*376A>G rs142349183
NM_015560.2(OPA1):c.*623G>A rs146468889
NM_015560.2(OPA1):c.*694C>A rs190367068
NM_015560.2(OPA1):c.*863A>G rs193292545
NM_015560.2(OPA1):c.-10C>T rs775614028
NM_015560.2(OPA1):c.-11C>G rs568049951
NM_015560.2(OPA1):c.1066-53T>G
NM_015560.2(OPA1):c.1071A>G (p.Ala357=) rs150807064
NM_015560.2(OPA1):c.1146A>G (p.Ile382Met) rs143319805
NM_015560.2(OPA1):c.1177A>C (p.Arg393=) rs149752576
NM_015560.2(OPA1):c.1212+10T>C rs200114656
NM_015560.2(OPA1):c.1212+38A>T
NM_015560.2(OPA1):c.1212+9A>G rs759086025
NM_015560.2(OPA1):c.1213-25G>C
NM_015560.2(OPA1):c.1242A>C (p.Thr414=) rs1553877924
NM_015560.2(OPA1):c.1313-141G>A
NM_015560.2(OPA1):c.1608A>C (p.Ala536=) rs78767626
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_1771-18delACTT rs765277368
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.205C>G (p.Pro69Ala) rs750775588
NM_015560.2(OPA1):c.2064G>A (p.Pro688=) rs768448865
NM_015560.2(OPA1):c.2166+115G>T
NM_015560.2(OPA1):c.2167-19C>A rs77355463
NM_015560.2(OPA1):c.2167-265T>G
NM_015560.2(OPA1):c.2276-134G>C
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
NM_015560.2(OPA1):c.239A>G (p.Tyr80Cys)
NM_015560.2(OPA1):c.2427T>C (p.Leu809=) rs145999595
NM_015560.2(OPA1):c.253C>T (p.Arg85Cys) rs372435892
NM_015560.2(OPA1):c.2613+11C>G rs111688935
NM_015560.2(OPA1):c.2614-149T>C
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>A (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.2808G>C (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.2819-4A>G rs184273607
NM_015560.2(OPA1):c.32+14C>T rs201927764
NM_015560.2(OPA1):c.321G>A (p.Ser107=) rs117888848
NM_015560.2(OPA1):c.420G>T (p.Val140=) rs35801538
NM_015560.2(OPA1):c.43C>A (p.Gln15Lys) rs75414918
NM_015560.2(OPA1):c.534A>G (p.Leu178=) rs758901451
NM_015560.2(OPA1):c.565G>A (p.Glu189Lys) rs569675223
NM_015560.2(OPA1):c.575C>T (p.Ala192Val) rs34307082
NM_015560.2(OPA1):c.6-13T>C rs1243357575
NM_015560.2(OPA1):c.624+235T>C
NM_015560.2(OPA1):c.625-5527G>T rs373326620
NM_015560.2(OPA1):c.679-279G>A
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.871-8G>T rs367618769
NM_015560.2(OPA1):c.871-9T>C rs531187028
NM_015560.2:c.2166+10T>C

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