ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.7308_7310dup (p.Thr2436_Lys2437insAsn)

dbSNP: rs2100305158
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 RCV001492206 SCV001696813 likely benign not provided 2020-07-02 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001492206 SCV005436234 likely benign not provided 2024-09-01 criteria provided, single submitter clinical testing MTOR: PM4:Supporting, BS2

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