Total submissions: 1
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Gene |
RCV000487128 | SCV000570341 | likely pathogenic | not provided | 2016-05-11 | criteria provided, single submitter | clinical testing | The T118I variant in the KRT14 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The T118I 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. The T118I variant is a non-conservative amino acid substitution, which occurs at a position within a known functional domain required for proper alignment of the keratin proteins into dimers. In silico analysis predicts this variant is probably damaging to the protein structure/function. In addition, numerous missense variants in nearby residues (K116E, K116N, M119I, M119T, M119V, Q120R, L122F, L122V, N123K, N123S) have been reported in the Human Gene Mutation Database in association with KRT14-related epidermolysis bullosa (Stenson et al., 2014), supporting the functional importance of this region of the protein. Therefore, we interpret T118I as a strong candidate for a pathogenic variant; however, the possibility it may be a rare benign variant cannot be excluded. |