List of variants in gene SMAD4 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: 29

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.*1820T>G	rs141309481	0.00426
NM_005359.6(SMAD4):c.*2968del	rs574286440	0.00280
NM_005359.6(SMAD4):c.1086T>C (p.Phe362=)	rs1801250	0.00228
NM_005359.6(SMAD4):c.1140-10T>C	rs186332162	0.00221
NM_005359.6(SMAD4):c.787+1_788-1del	rs1599189646	0.00095
NM_005359.6(SMAD4):c.*1874C>G	rs761701805	0.00053
NM_005359.6(SMAD4):c.880A>G (p.Met294Val)	rs7238500	0.00050
NM_005359.6(SMAD4):c.1392C>T (p.Ala464=)	rs140487104	0.00033
NM_005359.6(SMAD4):c.21G>A (p.Thr7=)	rs142292491	0.00010
NM_005359.6(SMAD4):c.424+5G>A	rs200772603	0.00010
NM_005359.6(SMAD4):c.852A>G (p.Gln284=)	rs144378484	0.00008
NM_005359.6(SMAD4):c.1647A>G (p.Gln549=)	rs113545983	0.00005
NM_005359.6(SMAD4):c.1218G>A (p.Ala406=)	rs145097078	0.00004
NM_005359.6(SMAD4):c.1644A>G (p.Pro548=)	rs756795016	0.00004
NM_005359.6(SMAD4):c.1611C>T (p.Asp537=)	rs369598262	0.00002
NM_005359.6(SMAD4):c.294C>T (p.Leu98=)	rs202126703	0.00002
NM_005359.6(SMAD4):c.1005A>G (p.Val335=)	rs878854762	0.00001
NM_005359.6(SMAD4):c.1492T>C (p.Leu498=)	rs1057520520	0.00001
NM_005359.6(SMAD4):c.276T>C (p.His92=)	rs762501162	0.00001
NM_005359.6(SMAD4):c.667+3G>A	rs757971589	0.00001
NM_005359.6(SMAD4):c.677C>T (p.Ala226Val)	rs539739051	0.00001
NM_005359.6(SMAD4):c.945C>T (p.Ser315=)	rs1408798906	0.00001
NM_005359.6(SMAD4):c.*3760dup	rs202070730
NM_005359.6(SMAD4):c.*6158GATT[1]	rs886053936
NM_005359.6(SMAD4):c.1311C>G (p.Val437=)	rs751539807
NM_005359.6(SMAD4):c.1632G>A (p.Pro544=)	rs549489716
NM_005359.6(SMAD4):c.454+2080A>C
NM_005359.6(SMAD4):c.479A>G (p.Asp160Gly)	rs1555685629
NM_005359.6(SMAD4):c.693C>A (p.Gly231=)

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