ClinVar Miner

Submissions for variant NM_002485.5(NBN):c.1785G>C (p.Met595Ile)

dbSNP: rs1586052885
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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 RCV001013174 SCV001173724 uncertain significance Hereditary cancer-predisposing syndrome 2019-07-17 criteria provided, single submitter clinical testing The p.M595I variant (also known as c.1785G>C), located in coding exon 11 of the NBN gene, results from a G to C substitution at nucleotide position 1785. The methionine at codon 595 is replaced by isoleucine, an amino acid with highly similar properties. This amino acid position is poorly 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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