ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 16
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_001276345.2(TNNT2):c.200-4C>G rs397516448
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529
NM_001276345.2(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.41+16A>G rs370729174
NM_001276345.2(TNNT2):c.52+7G>A rs374443596
NM_001276345.2(TNNT2):c.601-8C>T rs397516475
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032
NM_001276345.2(TNNT2):c.720-13_720-11del rs397516480
NM_001276345.2(TNNT2):c.720-4G>T rs201753429
NM_001276345.2(TNNT2):c.720-5T>G rs730881092
NM_001276345.2(TNNT2):c.720-6G>A rs113471285
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877
NM_001276345.2(TNNT2):c.97G>A (p.Glu33Lys) rs377474357

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