Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Labcorp Genetics |
RCV000056481 | SCV003441913 | pathogenic | not provided | 2022-06-20 | criteria provided, single submitter | clinical testing | This sequence change replaces isoleucine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 446 of the KRT10 protein (p.Ile446Thr). This variant is not present in population databases (gnomAD no frequency). This missense change has been observed in individuals with autosomal dominant KRT10-related conditions (PMID: 9856845). It has also been observed to segregate with disease in related individuals. ClinVar contains an entry for this variant (Variation ID: 66163). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt KRT10 protein function. For these reasons, this variant has been classified as Pathogenic. |
| Epithelial Biology; Institute of Medical Biology, |
RCV000056481 | SCV000087591 | not provided | not provided | no assertion provided | not provided | ||
| OMIM | RCV004595904 | SCV005088076 | pathogenic | Ichthyosis, annular epidermolytic 1 | 2024-02-07 | no assertion criteria provided | literature only |