ClinVar Miner

List of variants in gene TNNT2 reported as likely benign by Color Diagnostics, LLC DBA Color Health

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249 0.00046
NM_001276345.2(TNNT2):c.720-13_720-11del rs397516480 0.00031
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529 0.00009
NM_001276345.2(TNNT2):c.720-4G>T rs201753429 0.00009
NM_001276345.2(TNNT2):c.774C>T (p.Phe258=) rs397516481 0.00009
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877 0.00009
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086 0.00006
NM_001276345.2(TNNT2):c.295-14C>T rs747477576 0.00006
NM_001276345.2(TNNT2):c.430C>A (p.Arg144=) rs45525839 0.00006
NM_001276345.2(TNNT2):c.90C>T (p.Asp30=) rs727503515 0.00006
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474 0.00005
NM_001276345.2(TNNT2):c.864C>T (p.Arg288=) rs45503195 0.00005
NM_001276345.2(TNNT2):c.720-13C>G rs377714587 0.00004
NM_001276345.2(TNNT2):c.720-7C>T rs376303087 0.00004
NM_001276345.2(TNNT2):c.882C>T (p.Thr294=) rs45465693 0.00004
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827 0.00003
NM_001276345.2(TNNT2):c.552G>A (p.Lys184=) rs566113559 0.00003
NM_001276345.2(TNNT2):c.601-6G>A rs760197357 0.00003
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=) rs397516453 0.00002
NM_001276345.2(TNNT2):c.391G>A (p.Val131Ile) rs537067344 0.00002
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477 0.00002
NM_001276345.2(TNNT2):c.720-6G>A rs113471285 0.00002
NM_001276345.2(TNNT2):c.135G>A (p.Glu45=) rs756174289 0.00001
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909 0.00001
NM_001276345.2(TNNT2):c.153C>G (p.Thr51=) rs1347127737 0.00001
NM_001276345.2(TNNT2):c.164-11G>A rs1410150306 0.00001
NM_001276345.2(TNNT2):c.164-13G>A rs369469475 0.00001
NM_001276345.2(TNNT2):c.192G>A (p.Glu64=) rs1180516886 0.00001
NM_001276345.2(TNNT2):c.200-4C>G rs397516448 0.00001
NM_001276345.2(TNNT2):c.233+6T>C rs397516449 0.00001
NM_001276345.2(TNNT2):c.234-3C>T rs1361227759 0.00001
NM_001276345.2(TNNT2):c.24G>A (p.Val8=) rs1431025119 0.00001
NM_001276345.2(TNNT2):c.255G>A (p.Val85=) rs780115529 0.00001
NM_001276345.2(TNNT2):c.297C>T (p.Asp99=) rs771514445 0.00001
NM_001276345.2(TNNT2):c.33C>T (p.Tyr11=) rs148027842 0.00001
NM_001276345.2(TNNT2):c.390C>T (p.Leu130=) rs758543857 0.00001
NM_001276345.2(TNNT2):c.412-14C>A rs745721749 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.459G>A (p.Glu153=) rs775274966 0.00001
NM_001276345.2(TNNT2):c.610-6C>T rs45516702 0.00001
NM_001276345.2(TNNT2):c.68-9G>A rs1221903769 0.00001
NM_001276345.2(TNNT2):c.720-14C>A rs761998371 0.00001
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) rs754211195 0.00001
NM_001276345.2(TNNT2):c.-5A>G rs730881093
NM_001276345.2(TNNT2):c.102G>A (p.Gln34=) rs1660032754
NM_001276345.2(TNNT2):c.147G>A (p.Glu49=)
NM_001276345.2(TNNT2):c.200-12T>C rs1659753065
NM_001276345.2(TNNT2):c.200-6C>T rs1659750096
NM_001276345.2(TNNT2):c.207A>G (p.Pro69=) rs531954320
NM_001276345.2(TNNT2):c.213G>A (p.Glu71=)
NM_001276345.2(TNNT2):c.216G>A (p.Glu72=) rs2102273980
NM_001276345.2(TNNT2):c.231C>G (p.Pro77=) rs1659744526
NM_001276345.2(TNNT2):c.234-13C>T
NM_001276345.2(TNNT2):c.236C>T (p.Ser79Leu) rs761953142
NM_001276345.2(TNNT2):c.255G>T (p.Val85=) rs780115529
NM_001276345.2(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.295-15G>T rs1659456338
NM_001276345.2(TNNT2):c.321G>A (p.Lys107=) rs397516459
NM_001276345.2(TNNT2):c.369G>A (p.Arg123=) rs1558230929
NM_001276345.2(TNNT2):c.42-6T>C rs1660720268
NM_001276345.2(TNNT2):c.423G>C (p.Arg141=) rs2102253954
NM_001276345.2(TNNT2):c.432G>C (p.Arg144=)
NM_001276345.2(TNNT2):c.435C>G (p.Ala145=) rs375675827
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.570C>T (p.Asn190=) rs764636823
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.610-12C>T
NM_001276345.2(TNNT2):c.610-89C>T rs774177832
NM_001276345.2(TNNT2):c.610-9A>G rs939067295
NM_001276345.2(TNNT2):c.612A>G (p.Thr204=)
NM_001276345.2(TNNT2):c.627G>C (p.Gly209=) rs1658735553
NM_001276345.2(TNNT2):c.664C>T (p.Leu222=) rs2102234446
NM_001276345.2(TNNT2):c.693T>C (p.Ile231=)
NM_001276345.2(TNNT2):c.719+3G>A rs111451787
NM_001276345.2(TNNT2):c.720-10G>A rs2102229886
NM_001276345.2(TNNT2):c.720-6G>T rs113471285
NM_001276345.2(TNNT2):c.744G>A (p.Gln248=)
NM_001276345.2(TNNT2):c.747C>T (p.Ser249=) rs3020555
NM_001276345.2(TNNT2):c.789G>A (p.Lys263=) rs2102228724
NM_001276345.2(TNNT2):c.795G>A (p.Lys265=) rs1658577208
NM_001276345.2(TNNT2):c.834C>T (p.Ile278=) rs1278830616
NM_001276345.2(TNNT2):c.849A>G (p.Lys283=) rs2102216749
NM_001276345.2(TNNT2):c.852-3C>T rs749454768
NM_001276345.2(TNNT2):c.98-6C>T rs1335680363

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