ClinVar Miner

List of variants in gene TNNT2 reported as likely benign for Cardiovascular phenotype

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Total variants: 45
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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.692T>C (p.Ile231Thr) rs45520032 0.00015
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529 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.762G>T (p.Glu254Asp) rs45466197 0.00007
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086 0.00006
NM_001276345.2(TNNT2):c.430C>A (p.Arg144=) rs45525839 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.720-5T>G rs730881092 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.391G>A (p.Val131Ile) rs537067344 0.00002
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.192G>A (p.Glu64=) rs1180516886 0.00001
NM_001276345.2(TNNT2):c.21G>T (p.Val7=) rs777128825 0.00001
NM_001276345.2(TNNT2):c.390C>T (p.Leu130=) rs758543857 0.00001
NM_001276345.2(TNNT2):c.411C>T (p.Ile137=) rs727504322 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833 0.00001
NM_001276345.2(TNNT2):c.778C>T (p.Leu260=) rs977853063 0.00001
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) rs754211195 0.00001
NM_001276345.2(TNNT2):c.120G>A (p.Glu40=)
NM_001276345.2(TNNT2):c.171A>G (p.Glu57=)
NM_001276345.2(TNNT2):c.207A>G (p.Pro69=) rs531954320
NM_001276345.2(TNNT2):c.216G>A (p.Glu72=) rs2102273980
NM_001276345.2(TNNT2):c.228G>A (p.Lys76=) rs727504869
NM_001276345.2(TNNT2):c.237G>T (p.Ser79=) rs3729845
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.309G>A (p.Lys103=)
NM_001276345.2(TNNT2):c.357C>T (p.His119=)
NM_001276345.2(TNNT2):c.444G>A (p.Gln148=) rs2102253556
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.453G>C (p.Arg151=) rs786204406
NM_001276345.2(TNNT2):c.516G>A (p.Glu172=)
NM_001276345.2(TNNT2):c.531G>A (p.Lys177=)
NM_001276345.2(TNNT2):c.549G>A (p.Arg183=)
NM_001276345.2(TNNT2):c.666G>C (p.Leu222=)
NM_001276345.2(TNNT2):c.672G>A (p.Glu224=)
NM_001276345.2(TNNT2):c.771G>A (p.Lys257=)
NM_001276345.2(TNNT2):c.879C>T (p.Val293=)
NM_001276345.2(TNNT2):c.897G>A (p.Ter299=) rs1311267989

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