ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1391G>A (p.Trp464Ter)

dbSNP: rs2135959437
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics England Pilot Project, Genomics England RCV001542763 SCV001760247 likely pathogenic Familial meningioma no assertion criteria provided clinical testing

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