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: 54
Download table as spreadsheet
HGVS dbSNP
NC_000019.10:g.(?_55140863)_(55141322_?)del
NM_003283.6(TNNT1):c.116G>A (p.Arg39His)
NM_003283.6(TNNT1):c.11C>T (p.Thr4Ile) rs1568849957
NM_003283.6(TNNT1):c.129-5C>G rs997219637
NM_003283.6(TNNT1):c.136G>A (p.Val46Met)
NM_003283.6(TNNT1):c.139G>A (p.Val47Met) rs1599884701
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.200A>C (p.His67Pro) rs1555858107
NM_003283.6(TNNT1):c.200A>G (p.His67Arg) rs1555858107
NM_003283.6(TNNT1):c.202C>T (p.Arg68Cys)
NM_003283.6(TNNT1):c.207G>T (p.Lys69Asn)
NM_003283.6(TNNT1):c.26A>G (p.Tyr9Cys)
NM_003283.6(TNNT1):c.284A>G (p.Glu95Gly)
NM_003283.6(TNNT1):c.308T>C (p.Ile103Thr)
NM_003283.6(TNNT1):c.309+6C>T
NM_003283.6(TNNT1):c.310-8T>A
NM_003283.6(TNNT1):c.311A>T (p.Glu104Val)
NM_003283.6(TNNT1):c.31_32+1del rs944152647
NM_003283.6(TNNT1):c.32+4A>T
NM_003283.6(TNNT1):c.33-5C>T rs540523935
NM_003283.6(TNNT1):c.33-7T>G
NM_003283.6(TNNT1):c.355G>A (p.Glu119Lys) rs752992299
NM_003283.6(TNNT1):c.370C>T (p.Arg124Cys)
NM_003283.6(TNNT1):c.387+5G>A
NM_003283.6(TNNT1):c.387G>A (p.Ala129=) rs1415980730
NM_003283.6(TNNT1):c.388-11_388-8del rs1555857020
NM_003283.6(TNNT1):c.409G>A (p.Glu137Lys)
NM_003283.6(TNNT1):c.460C>G (p.Leu154Val)
NM_003283.6(TNNT1):c.487G>A (p.Gly163Ser)
NM_003283.6(TNNT1):c.508C>G (p.Gln170Glu) rs62126315
NM_003283.6(TNNT1):c.515G>A (p.Arg172His) rs749691780
NM_003283.6(TNNT1):c.523C>G (p.Arg175Gly) rs780372739
NM_003283.6(TNNT1):c.530C>T (p.Thr177Met) rs781338289
NM_003283.6(TNNT1):c.535C>T (p.Arg179Trp) rs757227738
NM_003283.6(TNNT1):c.550C>T (p.Arg184Cys)
NM_003283.6(TNNT1):c.562G>A (p.Glu188Lys)
NM_003283.6(TNNT1):c.566G>A (p.Arg189His) rs770079408
NM_003283.6(TNNT1):c.569A>G (p.Lys190Arg)
NM_003283.6(TNNT1):c.580G>A (p.Asp194Asn) rs141774400
NM_003283.6(TNNT1):c.585T>G (p.Ile195Met)
NM_003283.6(TNNT1):c.5C>G (p.Ser2Trp)
NM_003283.6(TNNT1):c.611G>A (p.Arg204Gln)
NM_003283.6(TNNT1):c.631C>A (p.Pro211Thr) rs766147911
NM_003283.6(TNNT1):c.653C>G (p.Pro218Arg)
NM_003283.6(TNNT1):c.711G>T (p.Lys237Asn)
NM_003283.6(TNNT1):c.723G>A (p.Met241Ile)
NM_003283.6(TNNT1):c.725C>T (p.Ala242Val) rs779112211
NM_003283.6(TNNT1):c.73G>A (p.Ala25Thr)
NM_003283.6(TNNT1):c.764A>G (p.Tyr255Cys) rs1599869703
NM_003283.6(TNNT1):c.77C>A (p.Pro26His)
NM_003283.6(TNNT1):c.788A>G (p.Lys263Arg) rs377276702
NM_003283.6(TNNT1):c.792-2A>G rs1555855228
NM_003283.6(TNNT1):c.802G>A (p.Ala268Thr) rs200340030

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.