ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.777C>G (p.Tyr259Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV003316921 SCV004018196 pathogenic Paragangliomas 5 2023-02-07 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation.

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