Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
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). |