ClinVar Miner

Variants in gene TNNT2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 17
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086
NM_001276345.2(TNNT2):c.163+12G>A rs45580032
NM_001276345.2(TNNT2):c.200-4C>G rs397516448
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_001276345.2(TNNT2):c.294+7G>A rs45490292
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=) rs3729547
NM_001276345.2(TNNT2):c.412-94del rs35559054
NM_001276345.2(TNNT2):c.42-20G>A rs45561443
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=) rs35914325
NM_001276345.2(TNNT2):c.52+7G>A rs374443596
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_001276345.2(TNNT2):c.68-5_68-3delinsTT rs397516362
NM_001276345.2(TNNT2):c.720-6G>A rs113471285
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238

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