ClinVar Miner

List of variants in gene TNNT2 reported as likely pathogenic by Stanford Center for Inherited Cardiovascular Disease,Stanford University

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Total variants: 9
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HGVS dbSNP
NM_000364.4(TNNT2):c.310C>T (p.Arg104Cys) rs727503513
NM_000364.4(TNNT2):c.311G>T (p.Arg104Leu) rs397516457
NM_000364.4(TNNT2):c.358T>C (p.Phe120Leu) rs121964858
NM_000364.4(TNNT2):c.418C>T (p.Arg140Cys) rs397516463
NM_000364.4(TNNT2):c.547C>T (p.Arg183Trp) rs727503512
NM_000364.4(TNNT2):c.548G>A (p.Arg183Gln) rs397516471
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.635G>A (p.Arg212Gln) rs121964860
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247

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