"Counsyl"[submitter] AND "SMAD4"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 183733	NM_005359.6(SMAD4):c.20C>T (p.Thr7Met)	SMAD4 (T7M)	Single nucleotide variant (missense variant)	Familial thoracic aortic aneurysm and aortic dissection +8 more	GConflicting classifications of pathogenicity
Select item 183887	NM_005359.6(SMAD4):c.21G>A (p.Thr7=)	SMAD4	Single nucleotide variant (synonymous variant)	Myhre syndrome +7 more	GConflicting classifications of pathogenicity
Select item 68788	NM_005359.6(SMAD4):c.38A>G (p.Asn13Ser)	SMAD4 (N13S)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 183699	NM_005359.6(SMAD4):c.102A>G (p.Thr34=)	SMAD4	Single nucleotide variant (synonymous variant)	not specified +6 more	GBenign/Likely benign
Select item 188234	NM_005359.6(SMAD4):c.172A>G (p.Ile58Val)	SMAD4 (I58V)	Single nucleotide variant (missense variant)	Juvenile polyposis syndrome +8 more	GUncertain significance
Select item 141740	NM_005359.6(SMAD4):c.175A>G (p.Thr59Ala)	SMAD4 (T59A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 372022	NM_005359.6(SMAD4):c.249+9T>C	SMAD4	Single nucleotide variant (intron variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +2 more	GLikely benign
Select item 327110	NM_005359.6(SMAD4):c.249+10A>C	SMAD4	Single nucleotide variant (intron variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +5 more	GConflicting classifications of pathogenicity
Select item 127950	NM_005359.6(SMAD4):c.424+5G>A	SMAD4	Single nucleotide variant (intron variant)	Familial thoracic aortic aneurysm and aortic dissection +7 more	GConflicting classifications of pathogenicity
Select item 460553	NM_005359.6(SMAD4):c.449G>A (p.Ser150Asn)	SMAD4 (S150N)	Single nucleotide variant (missense variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +4 more	GConflicting classifications of pathogenicity
Select item 188279	NM_005359.6(SMAD4):c.521C>A (p.Thr174Asn)	SMAD4 (T174N)	Single nucleotide variant (missense variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +6 more	GConflicting classifications of pathogenicity
Select item 185866	NM_005359.6(SMAD4):c.535A>G (p.Ile179Val)	SMAD4 (I179V)	Single nucleotide variant (missense variant)	Familial thoracic aortic aneurysm and aortic dissection +7 more	GUncertain significance
Select item 41789	NM_005359.6(SMAD4):c.565C>T (p.Arg189Cys)	SMAD4 (R189C)	Single nucleotide variant (missense variant)	Juvenile polyposis syndrome +6 more	GConflicting classifications of pathogenicity
Select item 136076	NM_005359.6(SMAD4):c.575C>T (p.Thr192Ile)	SMAD4 (T192I)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 220122	NM_005359.6(SMAD4):c.606C>G (p.Ala202=)	SMAD4	Single nucleotide variant (synonymous variant)	Generalized juvenile polyposis/juvenile polyposis coli +6 more	GBenign/Likely benign
Select item 378625	NM_005359.6(SMAD4):c.667+9T>C	SMAD4	Single nucleotide variant (intron variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +4 more	GBenign/Likely benign
Select item 136077	NM_005359.6(SMAD4):c.671A>T (p.Gln224Leu)	SMAD4 (Q224L)	Single nucleotide variant (missense variant)	Generalized juvenile polyposis/juvenile polyposis coli +8 more	GConflicting classifications of pathogenicity
Select item 215844	NM_005359.6(SMAD4):c.693C>T (p.Gly231=)	SMAD4	Single nucleotide variant (synonymous variant)	Generalized juvenile polyposis/juvenile polyposis coli +6 more	GBenign/Likely benign
Select item 185388	NM_005359.6(SMAD4):c.743A>T (p.Gln248Leu)	SMAD4 (Q248L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 183751	NM_005359.6(SMAD4):c.852A>G (p.Gln284=)	SMAD4	Single nucleotide variant (synonymous variant)	Juvenile polyposis syndrome +7 more	GConflicting classifications of pathogenicity
Select item 135244	NM_005359.6(SMAD4):c.880A>G (p.Met294Val)	SMAD4 (M294V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 548728	NM_005359.6(SMAD4):c.904T>C (p.Trp302Arg)	SMAD4 (W302R)	Single nucleotide variant (missense variant)	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome +2 more	GUncertain significance
Select item 245952	NM_005359.6(SMAD4):c.904+14T>C	SMAD4	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 219504	NM_005359.6(SMAD4):c.910G>A (p.Val304Ile)	SMAD4 (V304I)	Single nucleotide variant (missense variant)	Generalized juvenile polyposis/juvenile polyposis coli +5 more	GUncertain significance
Select item 135245	NM_005359.6(SMAD4):c.947A>G (p.Asn316Ser)	SMAD4 (N316S)	Single nucleotide variant (missense variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 492505	NM_005359.6(SMAD4):c.956-7C>T	SMAD4	Single nucleotide variant (intron variant)	Generalized juvenile polyposis/juvenile polyposis coli +2 more	GLikely benign
Select item 185189	NM_005359.6(SMAD4):c.1046C>T (p.Thr349Ile)	SMAD4 (T349I)	Single nucleotide variant (missense variant)	Juvenile polyposis syndrome +5 more	GConflicting classifications of pathogenicity
Select item 492460	NM_005359.6(SMAD4):c.1140-11T>A	SMAD4	Single nucleotide variant (intron variant)	Generalized juvenile polyposis/juvenile polyposis coli +3 more	GConflicting classifications of pathogenicity
Select item 185807	NM_005359.6(SMAD4):c.1248A>G (p.Arg416=)	SMAD4	Single nucleotide variant (synonymous variant)	Familial thoracic aortic aneurysm and aortic dissection +5 more	GConflicting classifications of pathogenicity
Select item 184070	NM_005359.6(SMAD4):c.1422A>C (p.Ser474=)	SMAD4	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +6 more	GBenign/Likely benign
Select item 41788	NM_005359.6(SMAD4):c.1573A>G (p.Ile525Val)	SMAD4 (I525V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 548845	NM_005359.6(SMAD4):c.1647del (p.Gln549fs)	SMAD4 (Q549fs)	Deletion (frameshift variant)	Generalized juvenile polyposis/juvenile polyposis coli +4 more	GUncertain significance
Select item 136074	NM_005359.6(SMAD4):c.1653A>G (p.Leu551=)	SMAD4	Single nucleotide variant (synonymous variant)	Myhre syndrome +7 more	GConflicting classifications of pathogenicity

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 33