ClinVar Miner

Submissions for variant NM_014844.5(TECPR2):c.3447C>T (p.Cys1149=)

dbSNP: rs2139755102
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001404906 SCV001606815 likely benign Hereditary spastic paraplegia 49 2023-06-17 criteria provided, single submitter clinical testing

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