ClinVar Miner

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

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857 0.00044
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197 0.00007
NM_001276345.2(TNNT2):c.863G>A (p.Arg288His) rs397516484 0.00005
NM_001276345.2(TNNT2):c.887G>A (p.Arg296His) rs141121678 0.00005
NM_001276345.2(TNNT2):c.720-7C>T rs376303087 0.00004
NM_001276345.2(TNNT2):c.810+5G>A rs730881113 0.00004
NM_001276345.2(TNNT2):c.411+6T>A rs761043932 0.00003
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245 0.00002
NM_001276345.2(TNNT2):c.34G>A (p.Glu12Lys) rs760247765 0.00002
NM_001276345.2(TNNT2):c.172G>A (p.Glu58Lys) rs1659923363 0.00001
NM_001276345.2(TNNT2):c.200-4C>G rs397516448 0.00001
NM_001276345.2(TNNT2):c.277G>A (p.Glu93Lys) rs727504244 0.00001
NM_001276345.2(TNNT2):c.452G>A (p.Arg151Gln) rs730881101 0.00001
NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn) rs141805127 0.00001
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540 0.00001
NM_001001430.2(TNNT2):c.580-45_580-20delins275
NM_001276345.2(TNNT2):c.-1C>T rs776936911
NM_001276345.2(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_001276345.2(TNNT2):c.233+3G>A
NM_001276345.2(TNNT2):c.268C>A (p.Pro90Thr) rs397516451
NM_001276345.2(TNNT2):c.279G>C (p.Glu93Asp) rs727503514
NM_001276345.2(TNNT2):c.281G>C (p.Arg94Thr) rs397516452
NM_001276345.2(TNNT2):c.282A>T (p.Arg94Ser) rs397516453
NM_001276345.2(TNNT2):c.300C>G (p.Ile100Met) rs1230932782
NM_001276345.2(TNNT2):c.313A>G (p.Met105Val) rs397516458
NM_001276345.2(TNNT2):c.316G>A (p.Glu106Lys) rs869312881
NM_001276345.2(TNNT2):c.406A>T (p.Arg136Trp) rs786204405
NM_001276345.2(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
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.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.611C>T (p.Thr204Ile) rs2102235172
NM_001276345.2(TNNT2):c.682G>T (p.Val228Leu) rs397516479
NM_001276345.2(TNNT2):c.719+12_719+28del
NM_001276345.2(TNNT2):c.719+5G>A rs1658715625
NM_001276345.2(TNNT2):c.720-6_720-3del rs1658597866
NM_001276345.2(TNNT2):c.782A>G (p.Gln261Arg) rs2102228802
NM_001276345.2(TNNT2):c.851+5G>A rs193922620
NM_001276345.2(TNNT2):c.870G>T (p.Lys290Asn) rs752111672
NM_001276345.2(TNNT2):c.98-4C>G rs775895925

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