ClinVar Miner

List of variants in gene TNNT2 reported as pathogenic for not provided

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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_000364.3(TNNT2):c.304C>T (p.Arg102Trp) rs397516456
NM_001001430.2(TNNT2):c.236T>A (p.Ile79Asn) rs121964855
NM_001001430.2(TNNT2):c.239C>T (p.Pro80Leu) rs730881121
NM_001001430.2(TNNT2):c.244G>A (p.Gly82Arg) rs727504255
NM_001001430.2(TNNT2):c.251dup (p.Val85Serfs) rs780087395
NM_001001430.2(TNNT2):c.275G>A (p.Arg92Gln) rs121964856
NM_001001430.2(TNNT2):c.275G>T (p.Arg92Leu) rs121964856
NM_001001430.2(TNNT2):c.280C>T (p.Arg94Cys) rs727503513
NM_001001430.2(TNNT2):c.281G>A (p.Arg94His) rs397516457
NM_001001430.2(TNNT2):c.281G>T (p.Arg94Leu) rs397516457
NM_001001430.2(TNNT2):c.319G>T (p.Glu107Ter) rs730881099
NM_001001430.2(TNNT2):c.328T>A (p.Phe110Ile) rs121964858
NM_001001430.2(TNNT2):c.388C>T (p.Arg130Cys) rs397516463
NM_001001430.2(TNNT2):c.391C>T (p.Arg131Trp) rs74315380
NM_001001430.2(TNNT2):c.392G>A (p.Arg131Gln) rs397516464
NM_001001430.2(TNNT2):c.416G>A (p.Arg139His) rs397516466
NM_001001430.2(TNNT2):c.421C>T (p.Arg141Trp) rs74315379
NM_001001430.2(TNNT2):c.487_489delGAG (p.Glu163del) rs397516470
NM_001001430.2(TNNT2):c.517C>T (p.Arg173Trp) rs727503512
NM_001001430.2(TNNT2):c.518G>A (p.Arg173Gln) rs397516471
NM_001001430.2(TNNT2):c.613C>T (p.Arg205Trp) rs45586240
NM_001001430.2(TNNT2):c.629_631delAGA (p.Lys210del) rs45578238
NM_001001430.2(TNNT2):c.817A>G (p.Lys273Glu) rs1553279294
NM_001001430.2(TNNT2):c.822-1G>T rs730881114
NM_001001430.2(TNNT2):c.822-2A>C rs111692981
NM_001001431.2(TNNT2):c.291G>T (p.Lys97Asn) rs397516459

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