ClinVar Miner

Submissions for variant NM_018116.4(MSTO1):c.1463C>T (p.Pro488Leu)

dbSNP: rs371544149
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002211113 SCV002496934 likely benign not provided 2023-12-01 criteria provided, single submitter clinical testing MSTO1: PP2, BP4, BS1
Breakthrough Genomics, Breakthrough Genomics RCV002211113 SCV005186942 uncertain significance not provided criteria provided, single submitter not provided

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