ClinVar Miner

List of variants in gene TNNT1 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_003283.6(TNNT1):c.388-151T>G rs2742062 0.41753
NM_003283.6(TNNT1):c.502-177A>G rs2562510 0.41611
NM_003283.6(TNNT1):c.193-88T>C rs2560942 0.40245
NM_003283.6(TNNT1):c.*160C>G rs10414711 0.26421
NM_003283.6(TNNT1):c.792-114C>T rs891186 0.23235
NM_003283.6(TNNT1):c.-12+30T>C rs28362592 0.22105
NM_003283.6(TNNT1):c.-11-161T>C rs75884999 0.21386
NM_003283.6(TNNT1):c.47-147A>G rs11550309 0.18678
NM_003283.6(TNNT1):c.611+201C>T rs3760873 0.17514
NM_003283.6(TNNT1):c.47-92C>G rs11550310 0.13442
NM_003283.6(TNNT1):c.47-13C>T rs11669534 0.11553
NM_003283.6(TNNT1):c.129-9T>G rs67795913 0.10318
NM_003283.6(TNNT1):c.-11-235C>T rs62126319 0.10280
NM_003283.6(TNNT1):c.107-108G>T rs2434454 0.09768
NM_003283.6(TNNT1):c.107-136A>T rs78156871 0.06835
NM_003283.6(TNNT1):c.751-42G>A rs74898598 0.06539
NM_003283.6(TNNT1):c.612-288G>T rs77062104 0.06107
NM_003283.6(TNNT1):c.-11-156C>G rs111759996 0.05295
NM_003283.6(TNNT1):c.388-260C>G rs145419596 0.04554
NM_003283.6(TNNT1):c.106+67G>A rs114353580 0.04503
NM_003283.6(TNNT1):c.-11-250A>G rs62126320 0.03930
NM_003283.6(TNNT1):c.751-16T>C rs77273500 0.03649
NM_003283.6(TNNT1):c.501+308G>A rs79705884 0.03344
NM_003283.6(TNNT1):c.193-42C>G rs73060953 0.03330
NM_003283.6(TNNT1):c.309+79G>A rs148264676 0.03212
NM_003283.6(TNNT1):c.192+97T>C rs113972150 0.02636
NM_003283.6(TNNT1):c.129-231A>G rs113672372 0.02427
NM_003283.6(TNNT1):c.192+74C>T rs7359930 0.01988
NM_003283.6(TNNT1):c.107-282G>T rs182143334 0.01484
NM_003283.6(TNNT1):c.-12+224C>T rs56029837 0.01369
NC_000019.10:g.55149387_55149388insT rs201667456 0.01193
NM_003283.6(TNNT1):c.501+71C>T rs115866474 0.00883
NM_003283.6(TNNT1):c.612-228A>G rs7259126 0.00853
NM_003283.6(TNNT1):c.-12+102G>C rs147570848 0.00810
NC_000019.10:g.55149294A>G rs73617684 0.00681
NM_003283.6(TNNT1):c.612-216G>A rs141880839 0.00671
NM_003283.6(TNNT1):c.-12+99G>A rs78609897 0.00657
NM_003283.6(TNNT1):c.310-14T>C rs115663668 0.00636
NM_003283.6(TNNT1):c.388-296G>A rs141764772 0.00597
NM_003283.6(TNNT1):c.792-243C>T rs55966503 0.00549
NM_003283.6(TNNT1):c.129-269G>A rs192289802 0.00517
NM_003283.6(TNNT1):c.791+206T>A rs563678746 0.00508
NM_003283.6(TNNT1):c.501+284T>C rs7259168 0.00488
NM_003283.6(TNNT1):c.107-112C>G rs115463201 0.00448
NM_003283.6(TNNT1):c.387+280G>T rs61218574 0.00448
NC_000019.10:g.55132607C>G rs149825397 0.00436
NM_003283.6(TNNT1):c.387+165T>G rs138034350 0.00381
NM_003283.6(TNNT1):c.310-105T>A rs143178872 0.00360
NC_000019.10:g.55149223_55149224insA rs147081925 0.00358
NM_003283.6(TNNT1):c.792-111G>T rs143223467 0.00300
NM_003283.6(TNNT1):c.279A>G (p.Glu93=) rs34313388 0.00277
NM_003283.6(TNNT1):c.128+17T>G rs201135309 0.00099
NM_003283.6(TNNT1):c.750+15C>T rs138664823 0.00086
NM_003283.6(TNNT1):c.791+12C>T rs201143291 0.00064
NM_003283.6(TNNT1):c.-12+15G>A rs539247551 0.00027
NM_003283.6(TNNT1):c.156G>A (p.Pro52=) rs369149321 0.00019
NM_003283.6(TNNT1):c.580G>A (p.Asp194Asn) rs141774400 0.00019
NM_003283.6(TNNT1):c.566G>A (p.Arg189His) rs770079408 0.00005
NM_003283.6(TNNT1):c.294C>T (p.Ala98=) rs373544170 0.00004
NM_003283.6(TNNT1):c.355G>A (p.Glu119Lys) rs752992299 0.00003
NM_003283.6(TNNT1):c.47-6C>G rs375682055 0.00003
NM_003283.6(TNNT1):c.144T>A (p.Pro48=) rs141999523 0.00001
NM_003283.6(TNNT1):c.310-4C>A rs1322730617 0.00001
NM_003283.6(TNNT1):c.523C>T (p.Arg175Trp) rs780372739 0.00001
NM_003283.6(TNNT1):c.129-240T>C rs112998815
NM_003283.6(TNNT1):c.192+207T>A rs2742058
NM_003283.6(TNNT1):c.193-174T>A rs77827923
NM_003283.6(TNNT1):c.193-218dup rs751662002
NM_003283.6(TNNT1):c.24A>G (p.Glu8=) rs1314161035
NM_003283.6(TNNT1):c.259G>A (p.Glu87Lys)
NM_003283.6(TNNT1):c.26A>G (p.Tyr9Cys) rs1449981150
NM_003283.6(TNNT1):c.32+8C>T rs371750770
NM_003283.6(TNNT1):c.387+152G>A rs149119868
NM_003283.6(TNNT1):c.387+74_387+75insATTATG rs200116583
NM_003283.6(TNNT1):c.388-221_388-219dup rs149328670
NM_003283.6(TNNT1):c.388-221dup rs149328670
NM_003283.6(TNNT1):c.388-267C>T rs138128632
NM_003283.6(TNNT1):c.46G>C (p.Glu16Gln) rs533504444
NM_003283.6(TNNT1):c.501+18_501+19del rs1555856952
NM_003283.6(TNNT1):c.502-199C>G rs7256092
NM_003283.6(TNNT1):c.562G>C (p.Glu188Gln)
NM_003283.6(TNNT1):c.611+12G>A rs376456377
NM_003283.6(TNNT1):c.751-42_751-35del rs36210101
NM_003283.6(TNNT1):c.751-5C>T rs192248377
NM_003283.6(TNNT1):c.791+192dup rs377688637
NM_003283.6(TNNT1):c.791+206del rs377688637
NM_003283.6(TNNT1):c.792-214A>C rs148326143
NM_003283.6(TNNT1):c.792-278C>A rs891185

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