ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3546G>T (p.Glu1182Asp)

dbSNP: rs1591637015
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001020570 SCV001182067 uncertain significance Hereditary cancer-predisposing syndrome 2019-03-12 criteria provided, single submitter clinical testing The p.E1182D variant (also known as c.3546G>T), located in coding exon 23 of the ATM gene, results from a G to T substitution at nucleotide position 3546. The glutamic acid at codon 1182 is replaced by aspartic acid, 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.

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