ClinVar Miner

List of variants in gene TNNT2 reported as likely pathogenic for Hypertrophic cardiomyopathy

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Total variants: 13
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HGVS dbSNP
NC_000001.11:g.201359651G>A
NM_000364.4(TNNT2):c.274G>A (p.Gly92Arg) rs727504255
NM_000364.4(TNNT2):c.287A>C (p.Asp96Ala) rs397516455
NM_000364.4(TNNT2):c.307A>C (p.Lys103Gln) rs730881122
NM_000364.4(TNNT2):c.311G>T (p.Arg104Leu) rs397516457
NM_000364.4(TNNT2):c.316_318del (p.Glu106del) rs727504277
NM_000364.4(TNNT2):c.321G>T (p.Lys107Asn) rs397516459
NM_000364.4(TNNT2):c.360T>G (p.Phe120Leu) rs727504331
NM_000364.4(TNNT2):c.566C>T (p.Ser189Phe) rs727504246
NM_000364.4(TNNT2):c.828C>A (p.Asn276Lys) rs376923877
NM_000364.4(TNNT2):c.842+1G>T rs111377893
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.882G>A (p.Trp294Ter) rs730881116

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