ClinVar Miner

List of variants in gene TNNT2 studied for Hypertrophic cardiomyopathy

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Total variants: 42
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HGVS dbSNP
NC_000001.11:g.201359651G>A
NM_000364.4(TNNT2):c.*66G>A rs3729998
NM_000364.4(TNNT2):c.-1C>A rs776936911
NM_000364.4(TNNT2):c.-22G>C rs886045829
NM_000364.4(TNNT2):c.-22G>T rs886045829
NM_000364.4(TNNT2):c.163+12G>A rs45580032
NM_000364.4(TNNT2):c.233+6T>C rs397516449
NM_000364.4(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_000364.4(TNNT2):c.266T>A (p.Ile89Asn) rs121964855
NM_000364.4(TNNT2):c.270C>G (p.Pro90=) rs140245123
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.294+7G>A rs45490292
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.307A>C (p.Lys103Gln) rs730881122
NM_000364.4(TNNT2):c.311G>A (p.Arg104His) rs397516457
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.348C>T (p.Ile116=) rs3729547
NM_000364.4(TNNT2):c.360T>G (p.Phe120Leu) rs727504331
NM_000364.4(TNNT2):c.418C>T (p.Arg140Cys) rs397516463
NM_000364.4(TNNT2):c.474G>C (p.Arg158=) rs35914325
NM_000364.4(TNNT2):c.508_510GAG[3] (p.Glu173del) rs397516470
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.53-11_53-7del rs45533739
NM_000364.4(TNNT2):c.566C>T (p.Ser189Phe) rs727504246
NM_000364.4(TNNT2):c.601-380C>T rs397516475
NM_000364.4(TNNT2):c.682A>G (p.Ile228Val) rs886045828
NM_000364.4(TNNT2):c.683T>C (p.Ile228Thr) rs45520032
NM_000364.4(TNNT2):c.711-5T>G rs730881092
NM_000364.4(TNNT2):c.711-9C>A rs763204242
NM_000364.4(TNNT2):c.779A>G (p.Lys260Arg) rs3730238
NM_000364.4(TNNT2):c.828C>A (p.Asn276Lys) rs376923877
NM_000364.4(TNNT2):c.842+1G>A rs111377893
NM_000364.4(TNNT2):c.842+1G>T rs111377893
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.875G>A (p.Gly292Glu) rs1272169178
NM_000364.4(TNNT2):c.877C>T (p.Arg293Cys) rs367785431
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247
NM_000364.4(TNNT2):c.882G>A (p.Trp294Ter) rs730881116

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