ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3298G>T (p.Asp1100Tyr)

dbSNP: rs1668850707
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Daryl Scott Lab, Baylor College of Medicine RCV001269287 SCV001448632 uncertain significance Noonan syndrome 4 2020-11-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004727066 SCV005330578 uncertain significance not provided 2024-08-01 criteria provided, single submitter clinical testing SOS1: PM2:Supporting

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