ClinVar Miner

List of variants in gene TNNT1 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 97
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003283.6(TNNT1):c.580G>A (p.Asp194Asn) rs141774400 0.00019
NM_003283.6(TNNT1):c.73G>A (p.Ala25Thr) rs372922115 0.00016
NM_003283.6(TNNT1):c.355G>A (p.Glu119Lys) rs752992299 0.00006
NM_003283.6(TNNT1):c.487G>A (p.Gly163Ser) rs374891900 0.00006
NM_003283.6(TNNT1):c.551G>A (p.Arg184His) rs759548188 0.00005
NM_003283.6(TNNT1):c.725C>T (p.Ala242Val) rs779112211 0.00005
NM_003283.6(TNNT1):c.562G>A (p.Glu188Lys) rs201519507 0.00004
NM_003283.6(TNNT1):c.566G>A (p.Arg189His) rs770079408 0.00004
NM_003283.6(TNNT1):c.73+6G>A rs1056384260 0.00004
NM_003283.6(TNNT1):c.802G>A (p.Ala268Thr) rs200340030 0.00004
NM_003283.6(TNNT1):c.387G>A (p.Ala129=) rs1415980730 0.00003
NM_003283.6(TNNT1):c.508C>G (p.Gln170Glu) rs62126315 0.00003
NM_003283.6(TNNT1):c.815G>A (p.Arg272His) rs533424787 0.00003
NM_003283.6(TNNT1):c.256T>G (p.Phe86Val) rs1222022158 0.00002
NM_003283.6(TNNT1):c.700G>A (p.Glu234Lys) rs1188124969 0.00002
NM_003283.6(TNNT1):c.769C>T (p.Arg257Cys) rs774943217 0.00002
NM_003283.6(TNNT1):c.793C>T (p.Arg265Trp) rs765317516 0.00002
NM_003283.6(TNNT1):c.128+5G>A rs769428135 0.00001
NM_003283.6(TNNT1):c.136G>A (p.Val46Met) rs778199645 0.00001
NM_003283.6(TNNT1):c.284A>G (p.Glu95Gly) rs1308212644 0.00001
NM_003283.6(TNNT1):c.308T>C (p.Ile103Thr) rs1050413432 0.00001
NM_003283.6(TNNT1):c.310-8T>A rs1322654025 0.00001
NM_003283.6(TNNT1):c.409G>A (p.Glu137Lys) rs1266457771 0.00001
NM_003283.6(TNNT1):c.515G>A (p.Arg172His) rs749691780 0.00001
NM_003283.6(TNNT1):c.530C>T (p.Thr177Met) rs781338289 0.00001
NM_003283.6(TNNT1):c.535C>T (p.Arg179Trp) rs757227738 0.00001
NM_003283.6(TNNT1):c.550C>T (p.Arg184Cys) rs12976760 0.00001
NM_003283.6(TNNT1):c.565C>T (p.Arg189Cys) rs780429876 0.00001
NM_003283.6(TNNT1):c.592A>G (p.Met198Val) rs757782018 0.00001
NM_003283.6(TNNT1):c.611G>A (p.Arg204Gln) rs765133367 0.00001
NM_003283.6(TNNT1):c.616C>T (p.Arg206Trp) rs748222508 0.00001
NM_003283.6(TNNT1):c.631C>A (p.Pro211Thr) rs766147911 0.00001
NM_003283.6(TNNT1):c.644C>T (p.Pro215Leu) rs1243419099 0.00001
NM_003283.6(TNNT1):c.71A>G (p.Glu24Gly) rs1391760195 0.00001
NM_003283.6(TNNT1):c.723G>A (p.Met241Ile) rs2085298945 0.00001
NM_003283.6(TNNT1):c.757G>A (p.Val253Met) rs572119503 0.00001
NM_003283.6(TNNT1):c.77C>A (p.Pro26His) rs1049167818 0.00001
NM_003283.6(TNNT1):c.788A>G (p.Lys263Arg) rs377276702 0.00001
NM_003283.6(TNNT1):c.817G>A (p.Val273Ile) rs774212109 0.00001
NM_003283.6(TNNT1):c.826C>T (p.Arg276Cys) rs201409131 0.00001
NM_003283.6(TNNT1):c.115C>A (p.Arg39Ser)
NM_003283.6(TNNT1):c.116G>A (p.Arg39His) rs1599891643
NM_003283.6(TNNT1):c.11C>T (p.Thr4Ile) rs1568849957
NM_003283.6(TNNT1):c.129-5C>G rs997219637
NM_003283.6(TNNT1):c.139G>A (p.Val47Met) rs1599884701
NM_003283.6(TNNT1):c.146C>G (p.Pro49Arg)
NM_003283.6(TNNT1):c.157C>T (p.Pro53Ser) rs755269853
NM_003283.6(TNNT1):c.16G>A (p.Glu6Lys) rs1599896616
NM_003283.6(TNNT1):c.192T>G (p.Asp64Glu)
NM_003283.6(TNNT1):c.263A>G (p.Gln88Arg) rs2147254988
NM_003283.6(TNNT1):c.26A>G (p.Tyr9Cys) rs1449981150
NM_003283.6(TNNT1):c.301G>A (p.Glu101Lys)
NM_003283.6(TNNT1):c.304C>A (p.Arg102Ser) rs774855200
NM_003283.6(TNNT1):c.309+6C>T rs932070035
NM_003283.6(TNNT1):c.311A>T (p.Glu104Val) rs2085441049
NM_003283.6(TNNT1):c.319C>T (p.Arg107Trp) rs755856894
NM_003283.6(TNNT1):c.31_32+1del rs944152647
NM_003283.6(TNNT1):c.32+4A>T rs780644788
NM_003283.6(TNNT1):c.320G>A (p.Arg107Gln) rs2147254128
NM_003283.6(TNNT1):c.33-7T>G rs771002524
NM_003283.6(TNNT1):c.370C>T (p.Arg124Cys) rs2085439112
NM_003283.6(TNNT1):c.376G>C (p.Ala126Pro)
NM_003283.6(TNNT1):c.387+5G>A rs2085438435
NM_003283.6(TNNT1):c.388-3C>G
NM_003283.6(TNNT1):c.401G>A (p.Arg134Lys)
NM_003283.6(TNNT1):c.428G>A (p.Arg143Gln)
NM_003283.6(TNNT1):c.46+6T>C
NM_003283.6(TNNT1):c.460C>G (p.Leu154Val) rs2085384859
NM_003283.6(TNNT1):c.46G>A (p.Glu16Lys) rs533504444
NM_003283.6(TNNT1):c.514C>T (p.Arg172Cys)
NM_003283.6(TNNT1):c.523C>G (p.Arg175Gly) rs780372739
NM_003283.6(TNNT1):c.536G>A (p.Arg179Gln) rs2147244813
NM_003283.6(TNNT1):c.554T>C (p.Ile185Thr) rs970200564
NM_003283.6(TNNT1):c.569A>G (p.Lys190Arg) rs2085359836
NM_003283.6(TNNT1):c.573G>T (p.Lys191Asn)
NM_003283.6(TNNT1):c.582C>A (p.Asp194Glu) rs2147244624
NM_003283.6(TNNT1):c.584T>C (p.Ile195Thr)
NM_003283.6(TNNT1):c.585T>G (p.Ile195Met) rs2085359369
NM_003283.6(TNNT1):c.589T>G (p.Tyr197Asp)
NM_003283.6(TNNT1):c.5C>G (p.Ser2Trp) rs1041234929
NM_003283.6(TNNT1):c.610C>T (p.Arg204Trp)
NM_003283.6(TNNT1):c.616C>G (p.Arg206Gly)
NM_003283.6(TNNT1):c.619T>C (p.Ser207Pro)
NM_003283.6(TNNT1):c.641A>G (p.Gln214Arg) rs2147236699
NM_003283.6(TNNT1):c.647C>G (p.Ser216Cys) rs1414740144
NM_003283.6(TNNT1):c.653C>G (p.Pro218Arg) rs2085300916
NM_003283.6(TNNT1):c.658A>T (p.Arg220Trp) rs113157106
NM_003283.6(TNNT1):c.711G>T (p.Lys237Asn) rs920784477
NM_003283.6(TNNT1):c.715G>A (p.Asp239Asn)
NM_003283.6(TNNT1):c.734A>T (p.Lys245Ile)
NM_003283.6(TNNT1):c.746A>G (p.Tyr249Cys)
NM_003283.6(TNNT1):c.764A>G (p.Tyr255Cys) rs1599869703
NM_003283.6(TNNT1):c.792-6C>G
NM_003283.6(TNNT1):c.799G>C (p.Gly267Arg)
NM_003283.6(TNNT1):c.81A>T (p.Glu27Asp) rs1267757904
NM_003283.6(TNNT1):c.89A>T (p.Glu30Val) rs2147267125
NM_003283.6(TNNT1):c.94G>T (p.Val32Leu) rs779711295

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.