ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.3901C>T (p.Arg1301Cys)

dbSNP: rs1646080085
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001368815 SCV001565228 benign not provided 2023-10-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001368815 SCV004703714 uncertain significance not provided 2024-02-01 criteria provided, single submitter clinical testing MTOR: PM2, PP3, PS2:Supporting

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