rs782495199

Description

The V456M variant has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. The V456M variant was not observed in approximately 6,400 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Across evolution, this substitution occurs at a position that is occupied by amino acids with properties similar to Valine. Additionally, in silico analysis predicts this variant is probably damaging to the protein structure/function. However, the V456M variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. Moreover, no missense mutations in nearby residues have been reported, indicating that this region of the protein may be tolerant of change. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic mutation or a rare benign variant. This variant was found in TAADV2-PANCARD