ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.1905C>T (p.His635=) (rs1020808836)

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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 RCV000575131 SCV000660769 likely benign Hereditary cancer-predisposing syndrome 2017-04-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
GeneDx RCV000478597 SCV000570851 uncertain significance not provided 2016-06-30 criteria provided, single submitter clinical testing This variant is denoted ATM c.1905C>T at the DNA level. This variant is silent at the coding level, preserving a Histidine at codon 635. This variant has not, to our knowledge, been published in the literature as being pathogenic or benign. In silico splicing models are uninformative, therefore, in the absence of RNA or functional studies, the actual effect of this variant is unknown. ATM c.1905C>T 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.The nucleotide which is altered, a cytosine (C) at base 1905, is not conserved. Based on currently available information, it is unclear whether ATM c.1905C>T is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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