Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Illumina Laboratory Services, |
RCV001152304 | SCV001313516 | uncertain significance | Autosomal recessive proximal renal tubular acidosis | 2018-01-12 | 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, |
RCV001152304 | SCV002775373 | uncertain significance | Autosomal recessive proximal renal tubular acidosis | 2022-05-23 | criteria provided, single submitter | clinical testing | |
| Labcorp Genetics |
RCV002557287 | SCV003495749 | uncertain significance | not provided | 2022-07-15 | criteria provided, single submitter | clinical testing | This sequence change affects codon 397 of the SLC4A4 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the SLC4A4 protein. It affects a nucleotide within the consensus splice site. This variant is present in population databases (rs200226048, gnomAD 0.05%). This variant has not been reported in the literature in individuals affected with SLC4A4-related conditions. ClinVar contains an entry for this variant (Variation ID: 904401). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing. 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. |