ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.8879C>T (p.Pro2960Leu)

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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 RCV003435320 SCV004157029 uncertain significance not provided 2022-08-01 criteria provided, single submitter clinical testing KMT2C: PM2:Supporting
Invitae RCV003435320 SCV004304497 benign not provided 2023-10-03 criteria provided, single submitter clinical testing

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