Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Institute for Genomic Statistics and Bioinformatics, |
RCV001171513 | SCV001245461 | likely pathogenic | DYRK1A-related intellectual disability syndrome | criteria provided, single submitter | clinical testing | The deleted amino acid is a highly conserved amino acid that is located in a tyrosine kinase domain. In population-related and phenotype-related databases, the variant is not listed. In the phenotype-related databases ClinVar and HGMD, a missense variant at the same amino acid position (c.563A> T; p.Lys188Ile) is recorded as likely pathogenic or pathogenic. In ClinVar, an in-frame deletion at position c.535_540del; p.Arg179_Val180del is also listed as likely to be pathogenic. The mutation prediction programs MutationTaster and PROVEAN estimate the variant found in the DYRK1A gene as pathogenic. To estimate a possible disruption of the splicing behavior due to the variant, we used various programs to predict splice points and splice enhancers using the Alamut software. The in-silica analysis gives no significant indication of a change in the splicing behavior. The ACMG classification of the variant is: probably pathogenic (Class 4: PS2, PM1, PM2, PP3). As an enzyme (protein kinase), the DYRK1A protein plays an important role in the differentiation, proliferation and survival of cells. Certain heterozygous variants in the DYRK1A gene have been associated with autosomal dominant mental retardation 7 (OMIM # 614104). This syndrome is characterized by developmental delays or reduced intelligence, autistic behavioral traits, stereotypes, microcephaly, seizures and dysmorphisms of the face and ears. Neonatal feeding disorders and cranial MRI abnormalities such as ventricular dilatation and corpus callosum hypoplasia have been described (reviews www.ncbi.nlm.nih.gov/books/NBK3334381). So far, different heterozygous missense, splice, nonsense and frame shift variants have been described as clearly causing the disease. | |
| Institute of Human Genetics, |
RCV001171513 | SCV002757823 | likely pathogenic | DYRK1A-related intellectual disability syndrome | 2020-01-20 | criteria provided, single submitter | clinical testing |