ClinVar Miner

List of variants in gene OPA1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NC_000003.12:g.193593196C>A
NM_015560.2(OPA1):c.*1815T>C rs570796106
NM_015560.2(OPA1):c.*1919T>A rs867799524
NM_015560.2(OPA1):c.*2156A>G rs886058258
NM_015560.2(OPA1):c.*2241A>G rs778074372
NM_015560.2(OPA1):c.*2283A>G rs886058259
NM_015560.2(OPA1):c.*2416C>T rs539683627
NM_015560.2(OPA1):c.*2605_*2607del rs886058260
NM_015560.2(OPA1):c.*260G>T rs886058256
NM_015560.2(OPA1):c.*2692G>A rs886058261
NM_015560.2(OPA1):c.*2694T>A rs886058262
NM_015560.2(OPA1):c.*2909A>T rs886058263
NM_015560.2(OPA1):c.*3147G>C rs886058264
NM_015560.2(OPA1):c.*322G>A rs886058257
NM_015560.2(OPA1):c.*56C>T rs564487151
NM_015560.2(OPA1):c.*622C>T rs750359704
NM_015560.2(OPA1):c.*694C>A rs190367068
NM_015560.2(OPA1):c.*863A>G rs193292545
NM_015560.2(OPA1):c.-102G>A rs886058255
NM_015560.2(OPA1):c.-10C>T rs775614028
NM_015560.2(OPA1):c.-8C>T rs371988066
NM_015560.2(OPA1):c.2276-4dup rs761286590
NM_015560.2(OPA1):c.2427T>C (p.Leu809=) rs145999595
NM_015560.2(OPA1):c.2797G>A (p.Val933Ile) rs375733283
NM_015560.2(OPA1):c.2808G>C (p.Ala936=) rs117475774
NM_015560.2(OPA1):c.625-4T>A rs374509936
NM_015560.2(OPA1):c.825C>T (p.Leu275=) rs201242590
NM_015560.2(OPA1):c.871-9T>C rs531187028
NM_015560.2(OPA1):c.88C>T (p.Leu30=) rs185976555
NM_015560.3(OPA1):c.*1039A>G
NM_015560.3(OPA1):c.*1131C>T
NM_015560.3(OPA1):c.*1266G>A
NM_015560.3(OPA1):c.*1581A>C
NM_015560.3(OPA1):c.*1884C>T
NM_015560.3(OPA1):c.*1920C>A
NM_015560.3(OPA1):c.*2170A>G
NM_015560.3(OPA1):c.*2234G>A
NM_015560.3(OPA1):c.*2801A>G
NM_015560.3(OPA1):c.*2839C>T
NM_015560.3(OPA1):c.*2861A>G
NM_015560.3(OPA1):c.*2902A>G
NM_015560.3(OPA1):c.*341G>T
NM_015560.3(OPA1):c.*403T>C
NM_015560.3(OPA1):c.*427A>T
NM_015560.3(OPA1):c.*614A>G
NM_015560.3(OPA1):c.*743G>C
NM_015560.3(OPA1):c.-144T>C
NM_015560.3(OPA1):c.-3G>A
NM_015560.3(OPA1):c.1426G>A (p.Val476Ile)
NM_015560.3(OPA1):c.1674G>A (p.Glu558=)
NM_015560.3(OPA1):c.2366A>G (p.Asn789Ser)
NM_015560.3(OPA1):c.2851G>A (p.Ala951Thr)
NM_015560.3(OPA1):c.556+2T>G
NM_015560.3(OPA1):c.686A>G (p.Tyr229Cys)
NM_015560.3(OPA1):c.820G>A (p.Val274Ile)

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