chr18:51065548:C>G Detail (hg38) (SMAD4)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr18:48,591,918-48,591,918 View the variant detail on this assembly version.
hg38	chr18:51,065,548-51,065,548

HGVS

SMAD4

Type	Transcript	Protein
RefSeq	NM_005359.5:c.1081C>G	NP_005350.1:p.Arg361Gly
Ensemble	ENST00000342988.8:c.1081C>G	ENST00000342988.8:p.Arg361Gly
	ENST00000398417.6:c.1081C>G	ENST00000398417.6:p.Arg361Gly
	ENST00000588745.5:c.793C>G	ENST00000588745.5:p.Arg265Gly
	ENST00000588860.6:c.1081C>G	ENST00000588860.6:p.Arg361Gly
	ENST00000589076.6:c.1081C>G	ENST00000589076.6:p.Arg361Gly
	ENST00000589941.2:c.1081C>G	ENST00000589941.2:p.Arg361Gly
	ENST00000590061.2:c.1081C>G	ENST00000590061.2:p.Arg361Gly
	ENST00000593223.2:c.1081C>G	ENST00000593223.2:p.Arg361Gly
	ENST00000714261.1:c.1120C>G	ENST00000714261.1:p.Arg374Gly
	ENST00000714264.1:c.1162C>G	ENST00000714264.1:p.Arg388Gly
	ENST00000714266.1:c.868C>G	ENST00000714266.1:p.Arg290Gly
	ENST00000714268.1:c.1051C>G	ENST00000714268.1:p.Arg351Gly
	ENST00000714269.1:c.1002+79C>G
	ENST00000714270.1:c.1159C>G	ENST00000714270.1:p.Arg387Gly
	ENST00000714272.1:c.1057C>G	ENST00000714272.1:p.Arg353Gly

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
Show details

Links

SMAD4

Type	Database	ID	Link
Gene	MIM	600993	OMIM
	HGNC	6770	HGNC
	Ensembl	ENSG00000141646	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM1158192	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2016-05-31	no assertion criteria provided	Breast neoplasm	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	gastric adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Neoplasm of uterine cervix	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	lung adenocarcinoma	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Neoplasm of the large intestine	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Carcinoma of esophagus	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	Squamous cell carcinoma of the head and neck	somatic	Detail
Likely pathogenic	2016-05-31	no assertion criteria provided	pancreatic adenocarcinoma	somatic	Detail
Pathogenic	2022-01-28	criteria provided, single submitter	juvenile polyposis syndrome	germline	Detail
Pathogenic	2021-05-06	criteria provided, single submitter	Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.588	juvenile polyposis syndrome	NA	CLINVAR		Detail
0.361	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)	NA	CLINVAR		Detail
0.122	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail
0.588	juvenile polyposis syndrome	Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account fo...	UNIPROT	9811934	Detail

Annotation

Annotations

Descrption	Source	Links
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Breast neoplasm	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Gastric adenocarcinoma	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Neoplasm of uterine cervix	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Lung adenocarcinoma	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Neoplasm of the large intestine	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Carcinoma of esophagus	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Squamous cell carcinoma of the head and neck	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Pancreatic adenocarcinoma	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Juvenile polyposis syndrome	ClinVar	Detail
NM_005359.6(SMAD4):c.1081C>G (p.Arg361Gly) AND Juvenile polyposis/hereditary hemorrhagic telangiecta...	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of case...	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs80338963 dbSNP
Genome: hg38
Position: chr18:51,065,548-51,065,548
Variant Type: snv
Reference Allele: C
Alternative Allele: G

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