ClinVar Miner

Submissions for variant NM_015335.5(MED13L):c.3779del (p.Ser1260fs)

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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 RCV003603496 SCV004395526 pathogenic Transposition of the great arteries, dextro-looped 2023-06-19 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ser1260Ilefs*40) in the MED13L gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MED13L are known to be pathogenic (PMID: 25712080, 25758992). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with MED13L-related conditions. For these reasons, this variant has been classified as Pathogenic.

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