List of variants in gene TNNT2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 12

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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.720-4G>T	rs201753429	0.00009
NM_001276345.2(TNNT2):c.774C>T (p.Phe258=)	rs397516481	0.00009
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=)	rs200283086	0.00006
NM_001276345.2(TNNT2):c.90C>T (p.Asp30=)	rs727503515	0.00006
NM_001276345.2(TNNT2):c.720-7C>T	rs376303087	0.00004
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=)	rs375675827	0.00003
NM_001276345.2(TNNT2):c.601-6G>A	rs760197357	0.00003
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=)	rs140245123
NM_001276345.2(TNNT2):c.53-22C>A	rs141800807
NM_001276345.2(TNNT2):c.810+64C>T

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