List of variants in gene TNNT2 reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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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.208A>G (p.Met70Val)	rs141837529	0.00009
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=)	rs376923877	0.00009
NM_001276345.2(TNNT2):c.52+7G>A	rs374443596	0.00007
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=)	rs200283086	0.00006
NM_001276345.2(TNNT2):c.601-8C>T	rs397516475	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.882C>T (p.Thr294=)	rs45465693	0.00004
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=)	rs200604266	0.00001
NM_001276345.2(TNNT2):c.108G>A (p.Glu36=)	rs1660030234
NM_001276345.2(TNNT2):c.267C>T (p.Ile89=)	rs1659523502
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=)	rs140245123
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=)	rs74315379
NM_001276345.2(TNNT2):c.543G>A (p.Glu181=)	rs2102245266
NM_001276345.2(TNNT2):c.885G>A (p.Gly295=)	rs2102212901

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