ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.357-4406A>G

dbSNP: rs879254318
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000236483 SCV000294173 uncertain significance not provided 2016-04-27 criteria provided, single submitter clinical testing The N3S variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. Data from control individuals was not available to assess whether N3S may be a common benign variant in the general population. The N3S variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Furthermore, the N3S variant occurs in an alternate transcript where no pathogenic variants have been reported in the Human Gene Mutation Database in association with LMNA-related disorders (Stenson et al., 2014). Nevertheless, this substitution occurs at a position that is conserved across species.

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