ClinVar Miner

Submissions for variant NM_152263.4(TPM3):c.229AAG[1] (p.Lys78del)

dbSNP: rs2148294430
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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 RCV001898939 SCV002175085 uncertain significance Congenital myopathy 4B, autosomal recessive; Congenital myopathy with fiber type disproportion 2022-11-01 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with TPM3-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.232_234del, results in the deletion of 1 amino acid(s) of the TPM3 protein (p.Lys78del), but otherwise preserves the integrity of the reading frame.

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