ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.554A>G (p.Asn185Ser) (rs730881079)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159238 SCV000209184 likely pathogenic not provided 2012-06-25 criteria provided, single submitter clinical testing The Asn185Ser variant in the TNNI3 gene has not been reported as a disease-causing mutation or as a benign polymorphism, to our knowledge. However, a mutation at the same position, Asn185Lys, has been reported in a 24 year-old patient with DCM and the patient's affected father, and the mutation was absent from 280 ethnically matched control chromosomes (Carballo S et al., 2009). Furthermore, mutations in nearby codons (Lys183Asn, Lys183Glu, Arg186Gln, Asp190Gly) have been reported in association with cardiomyopathy, supporting the functional importance of this region of the protein. The NHLBI ESP Exome Variant Server reports Asn185Ser was not observed in approximately 5,900 samples from individuals of European and African American backgrounds, indicating it is not a common variant in these populations. However, Asn185Ser is a conservative amino acid substitution of a larger, neutral, polar Asparagine with a smaller, neutral, polar Serine at a position that is not well conserved through evolution.In summary, with the clinical and molecular information available at this time, we cannot unequivocally determine the clinical significance of Asn185Ser in the TNNI3 gene, although evidence suggests it is likely disease-causing. The variant is found in HCM panel(s).

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