ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.105122C>T (p.Ser35041Phe)

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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 RCV002409864 SCV002673023 uncertain significance Cardiovascular phenotype 2020-03-17 criteria provided, single submitter clinical testing The p.S25976F variant (also known as c.77927C>T), located in coding exon 185 of the TTN gene, results from a C to T substitution at nucleotide position 77927. The serine at codon 25976 is replaced by phenylalanine, an amino acid with highly dissimilar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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