ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.4544del (p.Asn1515fs)

dbSNP: rs886041789
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000289342 SCV000330548 pathogenic not provided 2016-05-26 criteria provided, single submitter clinical testing The c.4544delA pathogenic variant in the TSC2 gene causes a frameshift starting with codon Asparagine 1515, changes this amino acid to a Threonine residue and creates a premature Stop codon at position 61 of the new reading frame, denoted p.Asn1515ThrfsX61. This pathogenic variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. Although this variant has not been previously reported to our knowledge, other frameshift variants have been reported in the TSC2 gene in association with tuberous sclerosis complex (TSC2 LOVD; Stenson et al., 2014).

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