ClinVar Miner

Submissions for variant NM_000368.4(TSC1):c.379G>A (p.Val127Ile) (rs372215435)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163960 SCV000214559 uncertain significance Hereditary cancer-predisposing syndrome 2017-12-15 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
GeneDx RCV000766818 SCV000590594 uncertain significance not provided 2017-06-19 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the TSC1 gene. The V127I variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. The V127I variant is not observed at a significant frequency in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The V127I variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. This substitution occurs at a position where amino acids with similar properties to Valine are tolerated across species. Additionally, the vast majority of TSC1 pathogenic variants result in protein truncation, while missense variants have been reported only rarely (Northrup et al., 2011; Au et al., 2007). However, multiple missense variants in nearby residues have been reported in Human Gene Mutation Database in association with tuberous sclerosis (Stenson et al., 2014), supporting the functional importance of this region of the protein. 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 variant or a rare benign variant.
Invitae RCV000527585 SCV000641654 benign Tuberous sclerosis 1 2017-12-07 criteria provided, single submitter clinical testing
PreventionGenetics RCV000241553 SCV000303870 likely benign not specified criteria provided, single submitter clinical testing

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