ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_000364.3(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_001001430.2(TNNT2):c.10A>C (p.Ile4Leu) rs139705141
NM_001001430.2(TNNT2):c.10A>G (p.Ile4Val)
NM_001001430.2(TNNT2):c.133+5G>A rs727504254
NM_001001430.2(TNNT2):c.133G>T (p.Glu45Ter) rs730881120
NM_001001430.2(TNNT2):c.203+9G>T rs1553283445
NM_001001430.2(TNNT2):c.217A>G (p.Asn73Asp) rs1060500235
NM_001001430.2(TNNT2):c.218A>G (p.Asn73Ser) rs397516450
NM_001001430.2(TNNT2):c.224T>G (p.Val75Gly) rs730881095
NM_001001430.2(TNNT2):c.230C>T (p.Pro77Leu) rs144900708
NM_001001430.2(TNNT2):c.238C>T (p.Pro80Ser) rs397516451
NM_001001430.2(TNNT2):c.251dup (p.Val85Serfs) rs780087395
NM_001001430.2(TNNT2):c.256G>A (p.Asp86Asn) rs1553282768
NM_001001430.2(TNNT2):c.264+6C>T rs758051932
NM_001001430.2(TNNT2):c.272A>T (p.His91Leu) rs1553282617
NM_001001430.2(TNNT2):c.294C>A (p.Asp98Glu) rs1553282545
NM_001001430.2(TNNT2):c.310G>C (p.Ala104Pro) rs1553282527
NM_001001430.2(TNNT2):c.317_318delTCinsCT (p.Ile106Thr) rs1553282523
NM_001001430.2(TNNT2):c.334A>G (p.Asn112Asp) rs1553282484
NM_001001430.2(TNNT2):c.34G>C (p.Glu12Gln) rs760247765
NM_001001430.2(TNNT2):c.361G>A (p.Val121Ile)
NM_001001430.2(TNNT2):c.381C>T (p.Ile127=) rs727504322
NM_001001430.2(TNNT2):c.382-6_382-4delCCT rs397516462
NM_001001430.2(TNNT2):c.392G>C (p.Arg131Pro) rs397516464
NM_001001430.2(TNNT2):c.406G>A (p.Glu136Lys) rs371142225
NM_001001430.2(TNNT2):c.408G>T (p.Glu136Asp) rs141754300
NM_001001430.2(TNNT2):c.40G>A (p.Glu14Lys) rs772890125
NM_001001430.2(TNNT2):c.416G>A (p.Arg139His) rs397516466
NM_001001430.2(TNNT2):c.421delC (p.Arg141Glyfs) rs730881115
NM_001001430.2(TNNT2):c.430C>T (p.Arg144Trp) rs483352832
NM_001001430.2(TNNT2):c.431G>A (p.Arg144Gln) rs745632066
NM_001001430.2(TNNT2):c.433G>A (p.Glu145Lys) rs984218824
NM_001001430.2(TNNT2):c.442C>T (p.Arg148Trp) rs730881123
NM_001001430.2(TNNT2):c.451C>T (p.Arg151Cys) rs45608937
NM_001001430.2(TNNT2):c.463G>T (p.Glu155Ter)
NM_001001430.2(TNNT2):c.472C>G (p.Arg158Gly) rs730881103
NM_001001430.2(TNNT2):c.476G>A (p.Arg159Gln) rs45501500
NM_001001430.2(TNNT2):c.52+6C>T rs397516472
NM_001001430.2(TNNT2):c.535T>G (p.Ser179Ala) rs377157235
NM_001001430.2(TNNT2):c.544A>T (p.Met182Leu) rs1553281184
NM_001001430.2(TNNT2):c.563T>C (p.Ile188Thr) rs878854148
NM_001001430.2(TNNT2):c.571-1G>A rs483352835
NM_001001430.2(TNNT2):c.579+3G>A
NM_001001430.2(TNNT2):c.587G>A (p.Arg196Gln) rs371047521
NM_001001430.2(TNNT2):c.647G>A (p.Arg216Lys) rs1205564576
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.676G>A (p.Glu226Lys) rs730881107
NM_001001430.2(TNNT2):c.690-9C>A rs763204242
NM_001001430.2(TNNT2):c.691G>C (p.Glu231Gln) rs1189945246
NM_001001430.2(TNNT2):c.70C>A (p.Gln24Lys)
NM_001001430.2(TNNT2):c.734C>T (p.Ala245Val) rs369181536
NM_001001430.2(TNNT2):c.745G>A (p.Asp249Asn) rs141805127
NM_001001430.2(TNNT2):c.749T>C (p.Leu250Pro) rs376037051
NM_001001430.2(TNNT2):c.773A>T (p.Lys258Ile) rs397516482
NM_001001430.2(TNNT2):c.776A>G (p.Tyr259Cys) rs1553280112
NM_001001430.2(TNNT2):c.778G>A (p.Glu260Lys) rs1131691898
NM_001001430.2(TNNT2):c.788T>C (p.Val263Ala) rs1553279354
NM_001001430.2(TNNT2):c.805A>G (p.Asn269Asp) rs4523540
NM_001001430.2(TNNT2):c.808G>T (p.Asp270Tyr) rs121964861
NM_001001430.2(TNNT2):c.80C>G (p.Ala27Gly)
NM_001001430.2(TNNT2):c.835G>A (p.Gly279Arg) rs757664792
NM_001001430.2(TNNT2):c.844A>G (p.Lys282Glu) rs1553279043
NM_001001430.2(TNNT2):c.853G>A (p.Gly285Arg) rs147940106
NM_001001430.2(TNNT2):c.856C>A (p.Arg286Ser)
NM_001001430.2(TNNT2):c.863A>C (p.Lys288Thr) rs770794082

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