ClinVar Miner

Submissions for variant NM_017849.3(TMEM127):c.447G>A (p.Trp149Ter) (rs121908829)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Familial Cancer Clinic,Veneto Institute of Oncology RCV000114832 SCV000148727 likely pathogenic - adrenal bilateral pheochromocy Pheochromocytoma no assertion criteria provided not provided Converted during submission to Likely pathogenic.

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