ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.69575C>T (p.Thr23192Ile)

gnomAD frequency: 0.00001  dbSNP: rs1319888327
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000607552 SCV000720028 likely benign not specified 2017-05-30 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Ambry Genetics RCV002331046 SCV002629685 uncertain significance Cardiovascular phenotype 2019-10-03 criteria provided, single submitter clinical testing The p.T14127I variant (also known as c.42380C>T), located in coding exon 152 of the TTN gene, results from a C to T substitution at nucleotide position 42380. The threonine at codon 14127 is replaced by isoleucine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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