ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.70009G>C (p.Glu23337Gln)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002330124 SCV002631769 uncertain significance Cardiovascular phenotype 2019-10-18 criteria provided, single submitter clinical testing The p.E14272Q variant (also known as c.42814G>C), located in coding exon 153 of the TTN gene, results from a G to C substitution at nucleotide position 42814. The glutamic acid at codon 14272 is replaced by glutamine, an amino acid with highly 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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