ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.4335C>G (p.Ile1445Met)

dbSNP: rs373960609
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000412831 SCV000492204 uncertain significance not specified 2016-11-29 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the NOTCH1 gene. The I1445M variant has not beenpublished as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. It was not observedin approximately 6,200 individuals of European and African American ancestry in the NHLBI Exome SequencingProject, indicating it is not a common benign variant in these populations. The I1445M variant is a conservativeamino acid substitution, which is not likely to impact secondary protein structure as these residues share similarproperties. In addition, this substitution occurs at a position where amino acids with similar properties to isoleucine(I) are tolerated across species. Nonetheless, methionine (M) is not wild type in any species, and in silico analysis isinconsistent in its predictions as to whether or not this variant is damaging to the protein structure/function.Therefore, based on the currently available information, it is unclear whether this variant is pathogenic or rare benign.This result cannot be interpreted for diagnosis or used for family member screening at this time.
Ambry Genetics RCV002314115 SCV000739484 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2023-05-11 criteria provided, single submitter clinical testing The p.I1445M variant (also known as c.4335C>G), located in coding exon 25 of the NOTCH1 gene, results from a C to G substitution at nucleotide position 4335. The isoleucine at codon 1445 is replaced by methionine, an amino acid with highly similar properties. 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 this alteration remains unclear.
Genome-Nilou Lab RCV002270244 SCV002553425 uncertain significance Adams-Oliver syndrome 5 2022-03-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002270243 SCV002553427 uncertain significance Aortic valve disease 1 2022-03-15 criteria provided, single submitter clinical testing
Invitae RCV002270244 SCV003256074 benign Adams-Oliver syndrome 5 2022-05-25 criteria provided, single submitter clinical testing

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