ClinVar Miner

List of variants in gene TNNT2 studied for Familial restrictive cardiomyopathy

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Total variants: 20
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HGVS dbSNP
NM_000364.3(TNNT2):c.294+7G>A rs45490292
NM_001001430.1(TNNT2):c.53-11_53-7delCTTCT rs45533739
NM_001001430.2(TNNT2):c.*66G>A rs3729998
NM_001001430.2(TNNT2):c.-1C>A rs776936911
NM_001001430.2(TNNT2):c.-22G>C rs886045829
NM_001001430.2(TNNT2):c.-22G>T rs886045829
NM_001001430.2(TNNT2):c.133+12G>A rs45580032
NM_001001430.2(TNNT2):c.203+6T>C rs397516449
NM_001001430.2(TNNT2):c.207G>A (p.Ser69=) rs3729845
NM_001001430.2(TNNT2):c.240C>G (p.Pro80=) rs140245123
NM_001001430.2(TNNT2):c.280C>T (p.Arg94Cys) rs727503513
NM_001001430.2(TNNT2):c.318C>T (p.Ile106=) rs3729547
NM_001001430.2(TNNT2):c.444G>C (p.Arg148=) rs35914325
NM_001001430.2(TNNT2):c.52+7G>A rs374443596
NM_001001430.2(TNNT2):c.571-8C>T rs397516475
NM_001001430.2(TNNT2):c.661A>G (p.Ile221Val) rs886045828
NM_001001430.2(TNNT2):c.662T>C (p.Ile221Thr) rs45520032
NM_001001430.2(TNNT2):c.690-5T>G rs730881092
NM_001001430.2(TNNT2):c.690-9C>A rs763204242
NM_001001430.2(TNNT2):c.758A>G (p.Lys253Arg) rs3730238

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