ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance by Invitae

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Gene type:
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Total variants: 84
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HGVS dbSNP
NM_000364.4(TNNT2):c.100C>A (p.Gln34Lys) rs1350800220
NM_000364.4(TNNT2):c.10A>C (p.Ile4Leu) rs139705141
NM_000364.4(TNNT2):c.10A>G (p.Ile4Val)
NM_000364.4(TNNT2):c.110C>G (p.Ala37Gly)
NM_000364.4(TNNT2):c.124G>A (p.Ala42Thr)
NM_000364.4(TNNT2):c.163+5G>A rs727504254
NM_000364.4(TNNT2):c.163G>T (p.Glu55Ter) rs730881120
NM_000364.4(TNNT2):c.233+9G>T rs1553283445
NM_000364.4(TNNT2):c.247A>G (p.Asn83Asp) rs1060500235
NM_000364.4(TNNT2):c.248A>G (p.Asn83Ser) rs397516450
NM_000364.4(TNNT2):c.254T>G (p.Val85Gly) rs730881095
NM_000364.4(TNNT2):c.260C>T (p.Pro87Leu) rs144900708
NM_000364.4(TNNT2):c.265A>T (p.Ile89Phe)
NM_000364.4(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
NM_000364.4(TNNT2):c.281dup (p.Val95fs) rs780087395
NM_000364.4(TNNT2):c.286G>A (p.Asp96Asn) rs1553282768
NM_000364.4(TNNT2):c.294+6C>T rs758051932
NM_000364.4(TNNT2):c.302A>T (p.His101Leu) rs1553282617
NM_000364.4(TNNT2):c.321G>T (p.Lys107Asn) rs397516459
NM_000364.4(TNNT2):c.324C>A (p.Asp108Glu) rs1553282545
NM_000364.4(TNNT2):c.340G>A (p.Ala114Thr)
NM_000364.4(TNNT2):c.340G>C (p.Ala114Pro) rs1553282527
NM_000364.4(TNNT2):c.347_348delinsCT (p.Ile116Thr) rs1553282523
NM_000364.4(TNNT2):c.34G>C (p.Glu12Gln) rs760247765
NM_000364.4(TNNT2):c.364A>G (p.Asn122Asp) rs1553282484
NM_000364.4(TNNT2):c.375del (p.Glu126fs)
NM_000364.4(TNNT2):c.391G>A (p.Val131Ile)
NM_000364.4(TNNT2):c.40G>A (p.Glu14Lys) rs772890125
NM_000364.4(TNNT2):c.411+6T>A rs761043932
NM_000364.4(TNNT2):c.411C>T (p.Ile137=) rs727504322
NM_000364.4(TNNT2):c.412-6_412-4del rs397516462
NM_000364.4(TNNT2):c.422G>C (p.Arg141Pro) rs397516464
NM_000364.4(TNNT2):c.436G>A (p.Glu146Lys) rs371142225
NM_000364.4(TNNT2):c.438G>T (p.Glu146Asp) rs141754300
NM_000364.4(TNNT2):c.446G>A (p.Arg149His) rs397516466
NM_000364.4(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_000364.4(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_000364.4(TNNT2):c.460C>T (p.Arg154Trp) rs483352832
NM_000364.4(TNNT2):c.461G>A (p.Arg154Gln) rs745632066
NM_000364.4(TNNT2):c.463G>A (p.Glu155Lys) rs984218824
NM_000364.4(TNNT2):c.472C>T (p.Arg158Trp) rs730881123
NM_000364.4(TNNT2):c.481C>T (p.Arg161Cys) rs45608937
NM_000364.4(TNNT2):c.493G>T (p.Glu165Ter) rs1558225837
NM_000364.4(TNNT2):c.502C>G (p.Arg168Gly) rs730881103
NM_000364.4(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_000364.4(TNNT2):c.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
NM_000364.4(TNNT2):c.52+6C>T rs397516472
NM_000364.4(TNNT2):c.557A>C (p.Lys186Thr)
NM_000364.4(TNNT2):c.557A>T (p.Lys186Met)
NM_000364.4(TNNT2):c.565T>G (p.Ser189Ala) rs377157235
NM_000364.4(TNNT2):c.574A>T (p.Met192Leu) rs1553281184
NM_000364.4(TNNT2):c.593T>C (p.Ile198Thr) rs878854148
NM_000364.4(TNNT2):c.600+5G>A
NM_000364.4(TNNT2):c.601-361G>A
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.603_604AG[1] (p.Glu202fs)
NM_000364.4(TNNT2):c.608G>A (p.Arg203Gln) rs371047521
NM_000364.4(TNNT2):c.668G>A (p.Arg223Lys) rs1205564576
NM_000364.4(TNNT2):c.682A>G (p.Ile228Val) rs886045828
NM_000364.4(TNNT2):c.683T>C (p.Ile228Thr) rs45520032
NM_000364.4(TNNT2):c.697G>A (p.Glu233Lys) rs730881107
NM_000364.4(TNNT2):c.711-9C>A rs763204242
NM_000364.4(TNNT2):c.712G>C (p.Glu238Gln) rs1189945246
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_000364.4(TNNT2):c.755C>T (p.Ala252Val) rs369181536
NM_000364.4(TNNT2):c.766G>A (p.Asp256Asn) rs141805127
NM_000364.4(TNNT2):c.770T>C (p.Leu257Pro) rs376037051
NM_000364.4(TNNT2):c.794A>T (p.Lys265Ile) rs397516482
NM_000364.4(TNNT2):c.797A>G (p.Tyr266Cys) rs1553280112
NM_000364.4(TNNT2):c.799G>A (p.Glu267Lys) rs1131691898
NM_000364.4(TNNT2):c.809T>C (p.Val270Ala) rs1553279354
NM_000364.4(TNNT2):c.814C>A (p.Arg272=)
NM_000364.4(TNNT2):c.826A>G (p.Asn276Asp) rs4523540
NM_000364.4(TNNT2):c.829G>T (p.Asp277Tyr) rs121964861
NM_000364.4(TNNT2):c.842+5G>A rs193922620
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.856G>A (p.Gly286Arg) rs757664792
NM_000364.4(TNNT2):c.856G>C (p.Gly286Arg)
NM_000364.4(TNNT2):c.865A>G (p.Lys289Glu) rs1553279043
NM_000364.4(TNNT2):c.874G>A (p.Gly292Arg) rs147940106
NM_000364.4(TNNT2):c.877C>A (p.Arg293Ser)
NM_000364.4(TNNT2):c.877C>T (p.Arg293Cys) rs367785431
NM_000364.4(TNNT2):c.878G>A (p.Arg293His) rs141121678
NM_000364.4(TNNT2):c.884A>C (p.Lys295Thr) rs770794082

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