List of variants in gene TNNT1 reported as uncertain significance by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003283.6(TNNT1):c.487G>A (p.Gly163Ser)	rs374891900	0.00006
NM_003283.6(TNNT1):c.178C>T (p.Arg60Cys)
NM_003283.6(TNNT1):c.256T>C (p.Phe86Leu)
NM_003283.6(TNNT1):c.32+5G>A	rs1555859876
NM_003283.6(TNNT1):c.647C>G (p.Ser216Cys)	rs1414740144
NM_003283.6(TNNT1):c.91C>T (p.Pro31Ser)

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