ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.1443C>T (p.Gly481=)

dbSNP: rs2540459742
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003736429 SCV004564416 likely benign not provided 2023-08-14 criteria provided, single submitter clinical testing

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