Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000486113 | SCV000567716 | pathogenic | not provided | 2015-08-14 | criteria provided, single submitter | clinical testing | The c.260_261dupTC duplication in the STXBP1 gene causes a frameshift starting with codon Isoleucine 88, changes this amino acid to a Serine residue and creates a premature Stop codon at position 33 of the new reading frame, denoted p.Ile88SerfsX33. This 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, we interpret it to be pathogenic. |
Génétique des Maladies du Développement, |
RCV001004751 | SCV001164230 | pathogenic | Developmental and epileptic encephalopathy, 4 | 2018-09-03 | criteria provided, single submitter | clinical testing | |
Genome |
RCV001265294 | SCV001443411 | pathogenic | Infantile epilepsy syndrome | 2019-03-11 | no assertion criteria provided | provider interpretation | Submission from Simons Searchlight facilitated by GenomeConnect. Variant interpreted by the Simons Searchlight team most recently on 2019-03-11 and interpreted as Pathogenic. Variant was initially reported on 2015-09-08 by GTR ID of laboratory name 26957. The reporting laboratory might also submit to ClinVar. |