ClinVar Miner

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

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Total variants: 26
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HGVS dbSNP
NM_000364.4(TNNT2):c.266T>A (p.Ile89Asn) rs121964855
NM_000364.4(TNNT2):c.304C>T (p.Arg102Trp) rs397516456
NM_000364.4(TNNT2):c.305G>A (p.Arg102Gln) rs121964856
NM_000364.4(TNNT2):c.305G>T (p.Arg102Leu) rs121964856
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.321G>T (p.Lys107Asn) rs397516459
NM_000364.4(TNNT2):c.358T>A (p.Phe120Ile) rs121964858
NM_000364.4(TNNT2):c.358T>C (p.Phe120Leu) rs121964858
NM_000364.4(TNNT2):c.358T>G (p.Phe120Val) rs121964858
NM_000364.4(TNNT2):c.418C>T (p.Arg140Cys) rs397516463
NM_000364.4(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_000364.4(TNNT2):c.508_510GAG[3] (p.Glu173del) rs397516470
NM_000364.4(TNNT2):c.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
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.564G>C (p.Leu188Phe) rs201270895
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.635G>A (p.Arg212Gln) rs121964860
NM_000364.4(TNNT2):c.641_643AGA[3] (p.Lys217del) rs45578238
NM_000364.4(TNNT2):c.826A>G (p.Asn276Asp) rs4523540
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.857G>A (p.Gly286Glu) rs727505233
NM_000364.4(TNNT2):c.878G>A (p.Arg293His) rs141121678
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247
NM_001001430.3(TNNT2):c.40_41+1del rs1558251170

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