Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000483089 | SCV000572544 | pathogenic | not provided | 2017-01-13 | criteria provided, single submitter | clinical testing | The c.4716delT variant in the MED13L gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The c.4716delT variant causes a frameshift starting with codon Proline 1573, changes this amino acid to a Leucine residue, and creates a premature Stop codon at position 27 of the new reading frame, denoted p.Pro1573LeufsX27. This variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. The c.4716delT variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. We interpret c.4716delT as a pathogenic variant. |
Genome |
RCV001265313 | SCV001443430 | pathogenic | Cardiac anomalies - developmental delay - facial dysmorphism syndrome | 2018-12-04 | no assertion criteria provided | provider interpretation | Submission from Simons Searchlight facilitated by GenomeConnect. Variant interpreted by the Simons Searchlight team most recently on 2018-12-04 and interpreted as Pathogenic. Variant was initially reported on 2017-01-18 by GTR ID of laboratory name 26957. The reporting laboratory might also submit to ClinVar. |