Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV001014993 | SCV001175774 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-09-30 | criteria provided, single submitter | clinical testing | The p.T76A variant (also known as c.226A>G), located in coding exon 3 of the NBN gene, results from an A to G substitution at nucleotide position 226. The threonine at codon 76 is replaced by alanine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. |