Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000215285 | SCV000278682 | uncertain significance | Hereditary cancer-predisposing syndrome | 2015-09-29 | criteria provided, single submitter | clinical testing | The p.A1700V variant (also known as c.5099C>T), located in coding exon 15 of the APC gene, results from a C to T substitution at nucleotide position 5099. The alanine at codon 1700 is replaced by valine, an amino acid with similar properties. This variant was not reported in population based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP), and 1000 Genomes Project. In the ESP, this variant was not observed in 6502 samples (13004 alleles) with coverage at this position. To date, this alteration has been detected with an allele frequency of approximately 0.003% (greater than 32000 alleles tested) in our clinical cohort. This amino acid position is not well conserved in available vertebrate species. 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 p.A1700V remains unclear. |
Baylor Genetics | RCV003475040 | SCV004204197 | uncertain significance | Familial adenomatous polyposis 1 | 2023-05-05 | criteria provided, single submitter | clinical testing |