ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.5914G>A (p.Asp1972Asn)

dbSNP: rs1414380652
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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 RCV002315094 SCV000739437 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2016-07-21 criteria provided, single submitter clinical testing The p.D1972N variant (also known as c.5914G>A), located in coding exon 31 of the NOTCH1 gene, results from a G to A substitution at nucleotide position 5914. The aspartic acid at codon 1972 is replaced by asparagine, an amino acid with highly 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 6475 samples (12950 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 alteration remains unclear.

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