ClinVar Miner

List of variants in gene TNNT1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_003283.6(TNNT1):c.-11-250A>G rs62126320 0.03981
NM_003283.6(TNNT1):c.193-42C>G rs73060953 0.03432
NM_003283.6(TNNT1):c.107-282G>T rs182143334 0.01484
NM_003283.6(TNNT1):c.-12+224C>T rs56029837 0.01475
NC_000019.10:g.55149387_55149388insT rs201667456 0.01193
NM_003283.6(TNNT1):c.612-228A>G rs7259126 0.00906
NM_003283.6(TNNT1):c.501+71C>T rs115866474 0.00883
NM_003283.6(TNNT1):c.-12+102G>C rs147570848 0.00830
NM_003283.6(TNNT1):c.612-216G>A rs141880839 0.00715
NC_000019.10:g.55149294A>G rs73617684 0.00681
NM_003283.6(TNNT1):c.-12+99G>A rs78609897 0.00657
NM_003283.6(TNNT1):c.388-296G>A rs141764772 0.00643
NM_003283.6(TNNT1):c.792-243C>T rs55966503 0.00588
NM_003283.6(TNNT1):c.791+206T>A rs563678746 0.00553
NM_003283.6(TNNT1):c.129-269G>A rs192289802 0.00517
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 0.00438
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 0.00292
NM_003283.6(TNNT1):c.750+15C>T rs138664823 0.00086
NM_003283.6(TNNT1):c.156G>A (p.Pro52=) rs369149321 0.00019
NM_003283.6(TNNT1):c.87G>A (p.Pro29=) rs930840597 0.00018
NM_003283.6(TNNT1):c.791+12C>T rs201143291 0.00006
NM_003283.6(TNNT1):c.193-218dup rs751662002
NM_003283.6(TNNT1):c.258C>T (p.Phe86=)
NM_003283.6(TNNT1):c.309+79G>A rs148264676
NM_003283.6(TNNT1):c.387+152G>A rs149119868
NM_003283.6(TNNT1):c.502-199C>G rs7256092
NM_003283.6(TNNT1):c.751-5C>T rs192248377
NM_003283.6(TNNT1):c.792-214A>C rs148326143

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