NM_015560.2(OPA1):c.2797G>A (p.Val933Ile) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Sep 19, 2020)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:

Allele description [Variation Report for NM_015560.2(OPA1):c.2797G>A (p.Val933Ile)]

NM_015560.2(OPA1):c.2797G>A (p.Val933Ile)

OPA1:OPA1 mitochondrial dynamin like GTPase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Genomic location:
Preferred name:
NM_015560.2(OPA1):c.2797G>A (p.Val933Ile)
  • NC_000003.12:g.193667259G>A
  • NG_011605.1:g.79116G>A
  • NM_001354663.2:c.2428G>A
  • NM_001354664.2:c.2425G>A
  • NM_015560.2:c.2797G>A
  • NM_130831.3:c.2689G>A
  • NM_130832.3:c.2743G>A
  • NM_130833.2:c.2800G>A
  • NM_130834.3:c.2851G>A
  • NM_130835.2:c.2854G>A
  • NM_130836.3:c.2908G>A
  • NM_130837.2:c.2962G>A
  • NP_001341592.1:p.Val810Ile
  • NP_001341593.1:p.Val809Ile
  • NP_056375.2:p.Val933Ile
  • NP_570844.1:p.Val897Ile
  • NP_570845.1:p.Val915Ile
  • NP_570846.1:p.Val934Ile
  • NP_570847.2:p.Val951Ile
  • NP_570848.1:p.Val952Ile
  • NP_570849.2:p.Val970Ile
  • NP_570850.2:p.Val988Ile
  • LRG_337t1:c.2797G>A
  • LRG_337t2:c.2962G>A
  • LRG_337:g.79116G>A
  • LRG_337p1:p.Val933Ile
  • LRG_337p2:p.Val988Ile
  • NC_000003.11:g.193385048G>A
Protein change:
dbSNP: rs375733283
NCBI 1000 Genomes Browser:
Molecular consequence:
  • NM_001354663.2:c.2428G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354664.2:c.2425G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015560.2:c.2797G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130831.3:c.2689G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130832.3:c.2743G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130833.2:c.2800G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130834.3:c.2851G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130835.2:c.2854G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130836.3:c.2908G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_130837.2:c.2962G>A - missense variant - [Sequence Ontology: SO:0001583]


MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
SCV000577786GeneDxcriteria provided, single submitter
Uncertain significance
(Sep 19, 2020)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000577786.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided


Not observed at a significant frequency in large population cohorts (Lek et al., 2016); In silico analysis supports that this missense variant does not alter protein structure/function; This variant is associated with the following publications: (PMID: 25794858, 20417568, 28926202, 31589614)

OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 26, 2021

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