Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002393824 | SCV002672659 | uncertain significance | Cardiovascular phenotype | 2021-10-11 | criteria provided, single submitter | clinical testing | The p.A251T variant (also known as c.751G>A), located in coding exon 4 of the SNTA1 gene, results from a G to A substitution at nucleotide position 751. The alanine at codon 251 is replaced by threonine, an amino acid with similar properties. This amino acid position is conserved. 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. |