ClinVar Miner

Submissions for variant NM_025136.4(OPA3):c.415C>T (p.Gln139Ter)

dbSNP: rs28937899
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000020909 SCV001338840 pathogenic 3-Methylglutaconic aciduria type 3 2008-12-01 no assertion criteria provided literature only
Counsyl RCV000020909 SCV000789568 likely pathogenic 3-Methylglutaconic aciduria type 3 2017-02-15 no assertion criteria provided clinical testing This submission and the accompanying classification are no longer maintained by the submitter. For more information on current observations and classification, please contact variantquestions@myriad.com.
GeneReviews RCV000020909 SCV000041515 not provided 3-Methylglutaconic aciduria type 3 no classification provided literature only Found in an individual of Indian origin with Costeff syndrome

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