ClinVar Miner

List of variants in gene TNNT1 studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
Download table as spreadsheet
HGVS dbSNP
NM_003283.6(TNNT1):c.*160C>G
NM_003283.6(TNNT1):c.-11-156C>G rs111759996
NM_003283.6(TNNT1):c.-11-161T>C rs75884999
NM_003283.6(TNNT1):c.-11-235C>T
NM_003283.6(TNNT1):c.-11-250A>G
NM_003283.6(TNNT1):c.-12+30T>C rs28362592
NM_003283.6(TNNT1):c.102G>A (p.Glu34=) rs766589504
NM_003283.6(TNNT1):c.106+4A>G
NM_003283.6(TNNT1):c.106+67G>A rs114353580
NM_003283.6(TNNT1):c.107-108G>T rs2434454
NM_003283.6(TNNT1):c.107-112C>G
NM_003283.6(TNNT1):c.107-136A>T rs78156871
NM_003283.6(TNNT1):c.107-282G>T
NM_003283.6(TNNT1):c.129-231A>G
NM_003283.6(TNNT1):c.129-240T>C
NM_003283.6(TNNT1):c.129-269G>A
NM_003283.6(TNNT1):c.156G>A (p.Pro52=) rs369149321
NM_003283.6(TNNT1):c.192+207T>A
NM_003283.6(TNNT1):c.192+74C>T
NM_003283.6(TNNT1):c.192+97T>C
NM_003283.6(TNNT1):c.193-174T>A rs77827923
NM_003283.6(TNNT1):c.193-218dup
NM_003283.6(TNNT1):c.193-24A>C
NM_003283.6(TNNT1):c.193-42C>G rs73060953
NM_003283.6(TNNT1):c.193-88T>C rs2560942
NM_003283.6(TNNT1):c.279A>G (p.Glu93=) rs34313388
NM_003283.6(TNNT1):c.309+1G>A
NM_003283.6(TNNT1):c.309+79G>A
NM_003283.6(TNNT1):c.310-105T>A
NM_003283.6(TNNT1):c.310-14T>C rs115663668
NM_003283.6(TNNT1):c.31_32+1del rs944152647
NM_003283.6(TNNT1):c.323C>G (p.Ser108Ter) rs727504177
NM_003283.6(TNNT1):c.345C>A (p.Arg115=) rs1599882425
NM_003283.6(TNNT1):c.387+152G>A rs149119868
NM_003283.6(TNNT1):c.387+165T>G
NM_003283.6(TNNT1):c.387+280G>T
NM_003283.6(TNNT1):c.387+74_387+75insATTATG
NM_003283.6(TNNT1):c.388-151T>G rs2742062
NM_003283.6(TNNT1):c.388-221_388-219dup
NM_003283.6(TNNT1):c.388-221dup
NM_003283.6(TNNT1):c.388-260C>G rs145419596
NM_003283.6(TNNT1):c.388-267C>T
NM_003283.6(TNNT1):c.388-296G>A
NM_003283.6(TNNT1):c.47-13C>T rs11669534
NM_003283.6(TNNT1):c.47-147A>G rs11550309
NM_003283.6(TNNT1):c.47-6C>G rs375682055
NM_003283.6(TNNT1):c.47-92C>G rs11550310
NM_003283.6(TNNT1):c.486C>T (p.Gly162=) rs746601153
NM_003283.6(TNNT1):c.501+284T>C
NM_003283.6(TNNT1):c.501+308G>A
NM_003283.6(TNNT1):c.501+71C>T rs115866474
NM_003283.6(TNNT1):c.502-177A>G rs2562510
NM_003283.6(TNNT1):c.502-199C>G
NM_003283.6(TNNT1):c.523C>T (p.Arg175Trp) rs780372739
NM_003283.6(TNNT1):c.538G>T (p.Glu180Ter) rs80358249
NM_003283.6(TNNT1):c.580G>A (p.Asp194Asn) rs141774400
NM_003283.6(TNNT1):c.611+201C>T rs3760873
NM_003283.6(TNNT1):c.612-216G>A
NM_003283.6(TNNT1):c.612-228A>G rs7259126
NM_003283.6(TNNT1):c.612-288G>T
NM_003283.6(TNNT1):c.73+10C>G rs1257429782
NM_003283.6(TNNT1):c.739C>T (p.Gln247Ter)
NM_003283.6(TNNT1):c.750+15C>T rs138664823
NM_003283.6(TNNT1):c.751-42G>A
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+12C>T rs201143291
NM_003283.6(TNNT1):c.791+192dup
NM_003283.6(TNNT1):c.791+206T>A
NM_003283.6(TNNT1):c.791+206del
NM_003283.6(TNNT1):c.792-111G>T
NM_003283.6(TNNT1):c.792-114C>T rs891186
NM_003283.6(TNNT1):c.792-214A>C
NM_003283.6(TNNT1):c.792-243C>T
NM_003283.6(TNNT1):c.792-278C>A rs891185
NM_003283.6(TNNT1):c.795G>T (p.Arg265=) rs890868
NM_003283.6(TNNT1):c.834G>A (p.Lys278=) rs929705577
Single allele

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.