ClinVar Miner

Submissions for variant NM_001323289.2(CDKL5):c.73G>A (p.Gly25Arg) (rs587783130)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000144802 SCV000191028 pathogenic not provided 2012-10-15 criteria provided, single submitter clinical testing This variant has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. The NHLBI ESP Exome Variant Project has not identified Gly25Arg in approximately 6,500 individuals of European or African American ethnicity, indicating that it is not a common benign variant in these populations. This amino acid substitution is non-conservative, as an uncharged, non-polar Glycine residue is replaced by a positively charged Arginine residue. Gly25Arg alters a highly conserved position in the ATP-binding domain of the protein, and multiple in silico algorithms predict it is damaging to protein structure/function. Additionally, the variant has been observed as a mosaic and de novo with validated parentage. The variant is found in EPILEPSY panel(s).

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