ClinVar Miner

Variants in gene TNNT2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 40
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=) rs3729547 0.69444
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845 0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238 0.05965
NM_001276345.2(TNNT2):c.*66G>A rs3729998 0.01883
NM_001276345.2(TNNT2):c.163+12G>A rs45580032 0.01441
NM_001276345.2(TNNT2):c.851+22C>T rs45495692 0.01327
NM_001276345.2(TNNT2):c.42-20G>A rs45561443 0.01192
NM_001276345.2(TNNT2):c.294+7G>A rs45490292 0.01066
NM_001276345.2(TNNT2):c.68-8A>G rs115805892 0.00864
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=) rs35914325 0.00788
NM_001276345.2(TNNT2):c.53-47C>G rs45553832 0.00345
NM_001276345.2(TNNT2):c.98-81G>A rs45576939 0.00067
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249 0.00046
NM_001276345.2(TNNT2):c.200-11A>G rs368658464 0.00021
NM_001276345.2(TNNT2):c.720-4G>T rs201753429 0.00009
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877 0.00009
NM_001276345.2(TNNT2):c.52+7G>A rs374443596 0.00007
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086 0.00006
NM_001276345.2(TNNT2):c.295-14C>T rs747477576 0.00006
NM_001276345.2(TNNT2):c.489+18C>T rs377743847 0.00006
NM_001276345.2(TNNT2):c.601-8C>T rs397516475 0.00006
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474 0.00005
NM_001276345.2(TNNT2):c.52+13G>A rs376820377 0.00004
NM_001276345.2(TNNT2):c.720-7C>T rs376303087 0.00004
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827 0.00003
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=) rs397516453 0.00002
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477 0.00002
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909 0.00001
NM_001276345.2(TNNT2):c.200-4C>G rs397516448 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833 0.00001
NM_001001430.3(TNNT2):c.68-1623_68-1621delinsTT rs397516362
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.412-6_412-4del rs397516462
NM_001276345.2(TNNT2):c.412-94del rs35559054
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.68-3C>T rs587780970
NM_001276345.2(TNNT2):c.68-5del rs2102295381
NM_001276345.2(TNNT2):c.719+13A>C rs563883763
NM_001276345.2(TNNT2):c.777C>T (p.Asp259=) rs2102228925

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