List of variants in gene TGFBR1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004612.4(TGFBR1):c.49C>T (p.Leu17=)	rs878854714	0.00020
NM_004612.4(TGFBR1):c.214A>T (p.Ile72Leu)	rs111513627	0.00019
NM_004612.4(TGFBR1):c.120C>T (p.Leu40=)	rs201267786	0.00011
NM_004612.4(TGFBR1):c.1065A>C (p.Ala355=)	rs758280185	0.00004
NM_004612.4(TGFBR1):c.933C>T (p.Ser311=)	rs200912890	0.00003
NM_004612.4(TGFBR1):c.897G>A (p.Val299=)	rs369881419	0.00001
NM_004612.4(TGFBR1):c.1284T>C (p.Tyr428=)	rs201163170
NM_004612.4(TGFBR1):c.423C>G (p.Leu141=)	rs1564153944
NM_004612.4(TGFBR1):c.52GCG[10] (p.Ala26dup)	rs11466445
NM_004612.4(TGFBR1):c.606G>C (p.Ala202=)	rs201497553

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