ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7884G>T (p.Gln2628His)

dbSNP: rs1554088722
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000580571 SCV000681894 uncertain significance Hereditary cancer-predisposing syndrome 2023-04-05 criteria provided, single submitter clinical testing This missense variant replaces glutamine with histidine at codon 2628 of the APC protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with APC-related disorders in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Ambry Genetics RCV000580571 SCV002676850 uncertain significance Hereditary cancer-predisposing syndrome 2021-03-28 criteria provided, single submitter clinical testing The p.Q2628H variant (also known as c.7884G>T), located in coding exon 15 of the APC gene, results from a G to T substitution at nucleotide position 7884. The glutamine at codon 2628 is replaced by histidine, an amino acid with highly similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.
Baylor Genetics RCV003459417 SCV004199410 uncertain significance Familial adenomatous polyposis 1 2023-10-10 criteria provided, single submitter clinical testing

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