ClinVar Miner

List of variants in gene TNNT2 reported as benign for not specified

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_000364.3(TNNT2):c.294+7G>A rs45490292
NM_000364.3(TNNT2):c.68-5_68-3delinsTT rs397516362
NM_001001430.1(TNNT2):c.53-11_53-7delCTTCT rs45533739
NM_001001430.2(TNNT2):c.133+12G>A rs45580032
NM_001001430.2(TNNT2):c.134-50G>A rs3729843
NM_001001430.2(TNNT2):c.170-29C>G rs45449197
NM_001001430.2(TNNT2):c.170-4C>G rs397516448
NM_001001430.2(TNNT2):c.207G>A (p.Ser69=) rs3729845
NM_001001430.2(TNNT2):c.265-19C>T rs587780969
NM_001001430.2(TNNT2):c.318C>T (p.Ile106=) rs3729547
NM_001001430.2(TNNT2):c.444G>C (p.Arg148=) rs35914325
NM_001001430.2(TNNT2):c.492C>T (p.Asn164=) rs483352833
NM_001001430.2(TNNT2):c.52+7G>A rs374443596
NM_001001430.2(TNNT2):c.571-32A>C rs1104859
NM_001001430.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001001430.2(TNNT2):c.68-1621C>T rs587780970
NM_001001430.2(TNNT2):c.68-1626A>G rs115805892
NM_001001430.2(TNNT2):c.690-6G>A rs113471285
NM_001001430.2(TNNT2):c.758A>G (p.Lys253Arg) rs3730238
NM_001001430.2(TNNT2):c.781-33C>T rs2275863
NM_001001430.2(TNNT2):c.821+22C>T rs45495692
NM_001001430.2(TNNT2):c.822-19C>T rs759855940
NM_001001430.2(TNNT2):c.84G>A (p.Ala28=) rs200283086

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