ClinVar Miner

Submissions for variant NM_194456.1(KRIT1):c.301G>A (p.Gly101Arg) (rs1057521140)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000427958 SCV000521193 likely pathogenic not provided 2016-06-24 criteria provided, single submitter clinical testing The G101R variant has been previously published in association with cerebral cavernous malformations (CCM) (Fisher et al., 2015) with limited data to fully support pathogenicity. G101R was not observed in approximately 6500 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 G101R variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is highly conserved across species, in silico analysis predicts this variant is probably damaging to the protein structure/function. Additionally, the variant has been observed to segregate with the disease. However, G101R is located in a loop of the gene's Nudix domain with no known functional importance (Fisher et al., 2015) and similar variants in nearby residues have not been reported in association with CCM (Stenson et al., 2014). Therefore, this variant is likely pathogenic; however, the possibility it is a benign variant cannot be excluded.
PreventionGenetics,PreventionGenetics RCV000427958 SCV000853032 uncertain significance not provided 2013-10-08 criteria provided, single submitter clinical testing

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