ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.5723C>T (p.Ala1908Val)

dbSNP: rs886039188
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002311216 SCV000320559 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2015-12-16 criteria provided, single submitter clinical testing The p.A1908V variant (also known as c.5723C>T), located in coding exon 31 of the NOTCH1 gene, results from a C to T substitution at nucleotide position 5723. The alanine at codon 1908 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 6363 samples (12726 alleles) with coverage at this position. This amino acid position is highly 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 this variant remains unclear.

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