Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV001024848 | SCV001186935 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-02-28 | criteria provided, single submitter | clinical testing | The p.E202V variant (also known as c.605A>T), located in coding exon 5 of the APC gene, results from an A to T substitution at nucleotide position 605. The glutamic acid at codon 202 is replaced by valine, an amino acid with dissimilar properties. This amino acid position is well 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. |