ClinVar Miner

Submissions for variant NM_015443.4(KANSL1):c.3298C>G (p.Gln1100Glu) (rs796052598)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000187789 SCV000241386 uncertain significance not provided 2014-07-28 criteria provided, single submitter clinical testing This variant is denoted p.Gln1100Glu (CAG>GAG): c.3298 C>G in exon 15 of the KANSL1 gene (NM_001193466.1). The Q1100E variant has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. It was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The Q1100E variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. However, this substitution occurs at a position that is not conserved across species. In addition, in silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic mutation or a rare benign variant. The variant is found in PME-EPI panel(s).

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