ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for Familial restrictive cardiomyopathy 3

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Total variants: 22
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001276345.2(TNNT2):c.*37C>G
NM_001276345.2(TNNT2):c.*37C>T
NM_001276345.2(TNNT2):c.*39C>T
NM_001276345.2(TNNT2):c.-1C>A rs776936911
NM_001276345.2(TNNT2):c.-22G>C rs886045829
NM_001276345.2(TNNT2):c.233+6T>C rs397516449
NM_001276345.2(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.313A>G (p.Met105Val) rs397516458
NM_001276345.2(TNNT2):c.52+7G>A rs374443596
NM_001276345.2(TNNT2):c.544G>T (p.Ala182Ser) rs730881097
NM_001276345.2(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001276345.2(TNNT2):c.67+12A>G
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032
NM_001276345.2(TNNT2):c.719+9T>C
NM_001276345.2(TNNT2):c.720-6G>A rs113471285
NM_001276345.2(TNNT2):c.720-7C>T rs376303087
NM_001276345.2(TNNT2):c.720-9C>A rs763204242
NM_001276345.2(TNNT2):c.810+7C>T
NM_001276345.2(TNNT2):c.810+8G>T
NM_001276345.2(TNNT2):c.851+5G>C rs193922620

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