ClinVar Miner

Submissions for variant NM_015560.2(OPA1):c.1847+1G>C (rs863224134)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000197138 SCV000251996 pathogenic not provided 2012-04-18 criteria provided, single submitter clinical testing IVS19+1 G>C, c.1847+1 G>C. The c.1847+1 G>C splice site mutation in the OPA1 gene destroys the canonical splice donor site in intron 19. It is predicted to cause abnormal gene splicing, either leading to an abnormal message that is subject to nonsense-mediated mRNA decay, or to an abnormal protein product if the message is used for protein translation. Although this mutation has not been previously reported to our knowledge, another mutation at the same position (c.1847+1 G>T) has been reported in association with Optic Atrophy 1 (Ferre et al., 2009). The variant is found in OAPEO-MITOP panel(s).

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