Description
p.Pro6Leu (CCT>CTT): c.17 C>T in exon 1 of the SMAD3 gene (NM_005902.3). The P6L variant in the SMAD3 gene has not been reported as a disease-causing mutation nor as a benign polymorphism to our knowledge. P6L was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The P6L variant is located at a position that is conserved across species, and in silico analysis predicts P6L is damaging to the protein structure/function. The P6L variant is a semi-conservative amino acid substitution as these residues share similar properties, but differ in size, charge, or other properties which may impact secondary structure. However, no missense mutations have been reported in nearby residues, indicating this region of the protein may tolerate change. With the clinical and molecular information available at this time, we cannot definitively determine if P6L is a disease-causing mutation or a rare benign variant. This variant was found in TAAD
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | yes | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
