ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.7450G>A (p.Val2484Ile) (rs587779864)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000565502 SCV000660581 likely benign Hereditary cancer-predisposing syndrome 2016-04-08 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other strong data supporting benign classification,In silico models in agreement (benign)
GeneDx RCV000115250 SCV000149159 uncertain significance not provided 2014-03-18 criteria provided, single submitter clinical testing This variant is denoted ATM c.7450G>A at the cDNA level, p.Val2484Ile (V2484I) at the protein level, and results in the change of a Valine to an Isoleucine (GTA>ATA). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. ATM Val2484Ile was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Since Valine and Isoleucine share similar properties, this is considered a conservative amino acid substitution and is unlikely to affect protein integrity. ATM Val2484Ile occurs at a position that is moderately conserved across species and is located in the FAT domain (UniProt). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available information, it is unclear whether ATM Val2484Ile is pathogenic or benign. We consider it to be a variant of uncertain significance.

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