Total submissions: 4
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Illumina Laboratory Services, |
RCV000333296 | SCV000440837 | uncertain significance | Cranioectodermal dysplasia 1 | 2018-01-13 | criteria provided, single submitter | clinical testing | This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease. |
| Fulgent Genetics, |
RCV000333296 | SCV002794186 | uncertain significance | Cranioectodermal dysplasia 1 | 2022-01-11 | criteria provided, single submitter | clinical testing | |
| Labcorp Genetics |
RCV000333296 | SCV003248221 | uncertain significance | Cranioectodermal dysplasia 1 | 2022-07-26 | criteria provided, single submitter | clinical testing | This sequence change replaces proline, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 918 of the IFT122 protein (p.Pro918Leu). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 343256). This variant has not been reported in the literature in individuals affected with IFT122-related conditions. This variant is present in population databases (rs147499719, gnomAD 0.006%). |
| Ambry Genetics | RCV004629194 | SCV005121062 | uncertain significance | Inborn genetic diseases | 2024-03-25 | criteria provided, single submitter | clinical testing | The c.2753C>T (p.P918L) alteration is located in exon 22 (coding exon 22) of the IFT122 gene. This alteration results from a C to T substitution at nucleotide position 2753, causing the proline (P) at amino acid position 918 to be replaced by a leucine (L). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. |