Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| 3billion, |
RCV002251239 | SCV002521795 | likely pathogenic | Intellectual disability, autosomal dominant 22 | 2022-05-22 | criteria provided, single submitter | clinical testing | Different pathogenic amino acid change has been reported with sufficient evidence at the same codon (ClinVar ID: VCV000440857,VCV000617452, PMID:27598823, 28283832). The variant is located in a well-established functional domain or exonic hotspot, where pathogenic variants have frequently reported. In silico prediction tools and conservation analysis predicted that this variant was probably damaging to the protein structure/function (3CNET: 0.973>=0.75). It is absent from the gnomAD v2.1.1 dataset. Therefore, this variant is classified as likely pathogenic according to the recommendation of ACMG/AMP guideline. |
| Broad Center for Mendelian Genomics, |
RCV004556095 | SCV005045234 | likely pathogenic | Intellectual disability | 2024-05-17 | criteria provided, single submitter | curation | The heterozygous p.Arg464Leu variant in ZBTB18 was identified by our study in one individual with intellectual developmental disorder. Trio exome analysis showed this variant to be de novo. The variant is absent from large population studies. This variant has been reported in ClinVar (Variation ID: 1687557) and has been interpreted as likely pathogenic by 3billion. Computational prediction tools and conservation analyses do not provide strong support for or against an impact to the protein. The number of missense variants reported in ZBTB18 in the general population is lower than expected, suggesting there is little benign variation in this gene and slightly increasing the possibility that a missense variant in this gene may not be tolerated. Two additional pathogenic variants, resulting in a different amino acid change at the same position, (p.Arg464Cys and Arg464His), have been reported in association with disease in the literature, supporting that a change at this position may not be tolerated (Variation IDs: 440857, 617452). In summary, although additional studies are required to fully establish its clinical significance, this variant is likely pathogenic for autosomal dominant intellectual developmental disorder 22. ACMG/AMP Criteria applied: PS2_Supporting, PM2_Supporting, PP2, PM5_Strong (Richards 2015). |