ClinVar Miner

List of variants in gene TNNT2 reported as likely benign by Color

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Gene type:
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Total variants: 62
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001276345.2(TNNT2):c.*3C>A
NM_001276345.2(TNNT2):c.-5A>G rs730881093
NM_001276345.2(TNNT2):c.102G>A (p.Gln34=)
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086
NM_001276345.2(TNNT2):c.135G>A (p.Glu45=)
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909
NM_001276345.2(TNNT2):c.153C>G (p.Thr51=) rs1347127737
NM_001276345.2(TNNT2):c.164-11G>A
NM_001276345.2(TNNT2):c.192G>A (p.Glu64=)
NM_001276345.2(TNNT2):c.200-12T>C
NM_001276345.2(TNNT2):c.200-4C>G rs397516448
NM_001276345.2(TNNT2):c.200-6C>T
NM_001276345.2(TNNT2):c.207A>G (p.Pro69=)
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529
NM_001276345.2(TNNT2):c.231C>G (p.Pro77=)
NM_001276345.2(TNNT2):c.233+6T>C rs397516449
NM_001276345.2(TNNT2):c.234-3C>T
NM_001276345.2(TNNT2):c.236C>T (p.Ser79Leu) rs761953142
NM_001276345.2(TNNT2):c.24G>A (p.Val8=)
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.282A>G (p.Arg94=)
NM_001276345.2(TNNT2):c.295-14C>T rs747477576
NM_001276345.2(TNNT2):c.295-15G>T
NM_001276345.2(TNNT2):c.321G>A (p.Lys107=)
NM_001276345.2(TNNT2):c.33C>T (p.Tyr11=) rs148027842
NM_001276345.2(TNNT2):c.369G>A (p.Arg123=) rs1558230929
NM_001276345.2(TNNT2):c.390C>T (p.Leu130=) rs758543857
NM_001276345.2(TNNT2):c.412-14C>A
NM_001276345.2(TNNT2):c.42-6T>C
NM_001276345.2(TNNT2):c.430C>A (p.Arg144=) rs45525839
NM_001276345.2(TNNT2):c.435C>G (p.Ala145=)
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.552G>A (p.Lys184=) rs566113559
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474
NM_001276345.2(TNNT2):c.601-6G>A rs760197357
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.610-6C>T rs45516702
NM_001276345.2(TNNT2):c.610-89C>T
NM_001276345.2(TNNT2):c.610-9A>G
NM_001276345.2(TNNT2):c.627G>C (p.Gly209=)
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001276345.2(TNNT2):c.68-9G>A rs1221903769
NM_001276345.2(TNNT2):c.719+3G>A
NM_001276345.2(TNNT2):c.720-13C>G rs377714587
NM_001276345.2(TNNT2):c.720-13_720-11del rs397516480
NM_001276345.2(TNNT2):c.720-14C>A
NM_001276345.2(TNNT2):c.720-4G>T rs201753429
NM_001276345.2(TNNT2):c.720-6G>A rs113471285
NM_001276345.2(TNNT2):c.720-7C>T rs376303087
NM_001276345.2(TNNT2):c.774C>T (p.Phe258=) rs397516481
NM_001276345.2(TNNT2):c.795G>A (p.Lys265=)
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877
NM_001276345.2(TNNT2):c.852-3C>T rs749454768
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) rs754211195
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.90C>T (p.Asp30=) rs727503515
NM_001276345.2(TNNT2):c.98-6C>T

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