ClinVar Miner

List of variants in gene TNNT2 reported by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001001430.2(TNNT2):c.580-45_580-20delins275
NM_001276345.2(TNNT2):c.-1C>T rs776936911
NM_001276345.2(TNNT2):c.108G>A (p.Glu36=)
NM_001276345.2(TNNT2):c.172G>A (p.Glu58Lys)
NM_001276345.2(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_001276345.2(TNNT2):c.200-4C>G rs397516448
NM_001276345.2(TNNT2):c.266T>A (p.Ile89Asn) rs121964855
NM_001276345.2(TNNT2):c.267C>T (p.Ile89=)
NM_001276345.2(TNNT2):c.282A>T (p.Arg94Ser) rs397516453
NM_001276345.2(TNNT2):c.300C>G (p.Ile100Met)
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245
NM_001276345.2(TNNT2):c.406A>T (p.Arg136Trp)
NM_001276345.2(TNNT2):c.411+6T>A rs761043932
NM_001276345.2(TNNT2):c.445C>T (p.Arg149Cys) rs397516465
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_001276345.2(TNNT2):c.460C>T (p.Arg154Trp) rs483352832
NM_001276345.2(TNNT2):c.52+7G>A rs374443596
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.552G>C (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.552G>T (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474
NM_001276345.2(TNNT2):c.572T>C (p.Met191Thr) rs869025538
NM_001276345.2(TNNT2):c.584G>A (p.Gly195Glu) rs1558224822
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001276345.2(TNNT2):c.643C>T (p.Arg215Trp) rs45586240
NM_001276345.2(TNNT2):c.719+5G>A
NM_001276345.2(TNNT2):c.720-6_720-3del
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197
NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile) rs397516482
NM_001276345.2(TNNT2):c.810+5G>A rs730881113
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540
NM_001276345.2(TNNT2):c.851+5G>A rs193922620
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857
NM_001276345.2(TNNT2):c.863G>C (p.Arg288Pro) rs397516484
NM_001276345.2(TNNT2):c.864C>T (p.Arg288=) rs45503195
NM_001276345.2(TNNT2):c.882C>T (p.Thr294=) rs45465693
NM_001276345.2(TNNT2):c.890G>A (p.Trp297Ter) rs727504247
NM_001276345.2(TNNT2):c.98-4C>G rs775895925

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.