ClinVar Miner

Submissions for variant NM_001130438.3(SPTAN1):c.1040G>A (p.Arg347His) (rs796053314)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000717525 SCV000848378 uncertain significance Seizures 2016-11-30 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
GeneDx RCV000189489 SCV000243132 uncertain significance not provided 2012-07-16 criteria provided, single submitter clinical testing p.Arg347His (CGC>CAC): c.1040 G>A in exon 8 of the SPTAN1 gene (NM_001130438.1) The Arg347His variant in the SPTAN1 gene 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 Arg347His in approximately 5,000 individuals of European or African American ethnicity, indicating that it is not a common benign variant in these populations. Data from population-matched controls are not available. Previously reported pathogenic mutations in SPTAN1 include in-frame deletions or duplications located in the last four spectrin repeats that are essential for dimerization (Saitsu et al., 2010), whereas the Arg347 residue is outside this region. Additionally, this amino acid substitution is conservative, as both Arginine and Histidine are positively charged amino acids. Some in silico models predict that the Arg347His substitution is damaging to protein structure/function but others classify it as a likely benign change. Based on the information currently available, it is unclear whether Arg347His is a disease-causing mutation or a rare benign variant. The variant is found in INFANT-EPI panel(s).

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