ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.432_437dup (p.Arg145_Arg146dup)

dbSNP: rs2085712282
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001236831 SCV001409569 uncertain significance Hypertrophic cardiomyopathy 2022-10-07 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. ClinVar contains an entry for this variant (Variation ID: 962897). This variant has been observed in individual(s) with clinical features of hypertrophic cardiomyopathy (Invitae). This variant is not present in population databases (gnomAD no frequency). This variant, c.432_437dup, results in the insertion of 2 amino acid(s) of the TNNI3 protein (p.Arg145_Arg146dup), but otherwise preserves the integrity of the reading frame.

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