Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001008955 | SCV001168763 | likely pathogenic | not provided | 2018-08-10 | criteria provided, single submitter | clinical testing | The c.4232_4233delGA pathogenic variant in the TRIOBP gene causes a frameshift starting with codon Arginine 1411, changes this amino acid to a Threonine residue and creates a premature Stop codon at position 30 of the new reading frame, denoted p.Arg1411ThrfsX30. This pathogenic variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. Although this pathogenic variant has not been previously reported to our knowledge, we consider this to be a likely pathogenic variant. |