ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.9160G>A (p.Glu3054Lys)

dbSNP: rs397517779
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000040884 SCV000064575 uncertain significance not specified 2012-11-30 criteria provided, single submitter clinical testing The Glu3054Lys variant in TTN has not been reported in the literature nor previo usly identified by our laboratory. This variant has not been identified in large and broad European American and African American populations by the NHLBI Exome Sequencing Project (http://evs.gs.washington.edu/EVS/), though it remains possi ble that this variant is common in other populations. Computational analyses (bi ochemical amino acid properties, conservation, AlignGVGD, PolyPhen2, and SIFT) s uggest that the Glu3054Lys variant may impact the protein, though this informati on is not predictive enough to determine pathogenicity. In summary, additional i nformation is needed to fully assess the clinical significance of this variant.

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