ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.9472-3C>T

dbSNP: rs1553988133
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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 RCV000620858 SCV000736057 uncertain significance Cardiovascular phenotype 2017-10-12 criteria provided, single submitter clinical testing The c.9334-3C>T intronic variant results from a C to T substitution 3 nucleotides upstream from coding exon 39 in the TTN gene. This nucleotide position is poorly conserved in available vertebrate species. Using the BDGP and ESEfinder splice site prediction tools, this alteration is not predicted to have any significant effect on this splice acceptor site; however, direct evidence is unavailable. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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