List of variants in gene TBX5 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_181486.4(TBX5):c.787G>A (p.Val263Met)	rs147405081	0.00423
NM_181486.4(TBX5):c.331G>T (p.Asp111Tyr)	rs77357563	0.00382
NM_181486.4(TBX5):c.316A>G (p.Ile106Val)	rs147710408	0.00086
NM_181486.4(TBX5):c.834T>C (p.Ser278=)	rs142609815	0.00014
NM_181486.4(TBX5):c.1233C>G (p.Thr411=)	rs188839350	0.00008
NM_181486.4(TBX5):c.375C>T (p.Gly125=)	rs142293206	0.00002
NM_181486.4(TBX5):c.483C>G (p.Thr161=)	rs756481812

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