chr18:48604707:G>T Detail (hg19) (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	chr18:48,604,707-48,604,707
hg38	chr18:51,078,337-51,078,337 View the variant detail on this assembly version.

HGVS

SMAD4

Type	Transcript	Protein
RefSeq	NM_005359.5:c.1529G>T	NP_005350.1:p.Gly510Val
Ensemble	ENST00000398417.6:c.1529G>T	ENST00000398417.6:p.Gly510Val
	ENST00000593223.2:c.*1526G>T
	ENST00000342988.8:c.1529G>T	ENST00000342988.8:p.Gly510Val
	ENST00000588745.5:c.1241G>T	ENST00000588745.5:p.Gly414Val
	ENST00000588860.6:c.1529G>T	ENST00000588860.6:p.Gly510Val
	ENST00000589076.6:c.1529G>T	ENST00000589076.6:p.Gly510Val
	ENST00000589941.2:c.1529G>T	ENST00000589941.2:p.Gly510Val
	ENST00000590061.2:c.1529G>T	ENST00000590061.2:p.Gly510Val
	ENST00000714261.1:c.1568G>T	ENST00000714261.1:p.Gly523Val
	ENST00000714264.1:c.1610G>T	ENST00000714264.1:p.Gly537Val
	ENST00000714266.1:c.1316G>T	ENST00000714266.1:p.Gly439Val
	ENST00000714268.1:c.1499G>T	ENST00000714268.1:p.Gly500Val
	ENST00000714269.1:c.1301G>T	ENST00000714269.1:p.Gly434Val
	ENST00000714270.1:c.1607G>T	ENST00000714270.1:p.Gly536Val
	ENST00000714272.1:c.1505G>T	ENST00000714272.1:p.Gly502Val

Summary

MGeND

Clinical significance	not provided
Variant entry	2
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely 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	COSM1151558	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
not provided		sigmoid colon	not provided	MGS000040 (TMGS000095)	Hitoshi Nakagama	National Cancer Center Japan
not provided		Non-small cell lung cancer	somatic	MGS000018 (TMGS000110)	Hitoshi Nakagama	National Cancer Center Japan	30742731

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2015-11-25	criteria provided, single submitter	Hereditary cancer-predisposing syndrome,Familial thoracic aortic aneurysm and aortic dissection	germline	Detail
Likely pathogenic	2015-11-25	criteria provided, single submitter	Hereditary cancer-predisposing syndrome,Familial thoracic aortic aneurysm and aortic dissection	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.588	juvenile polyposis syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_005359.6(SMAD4):c.1529G>T (p.Gly510Val) AND multiple conditions	ClinVar	Detail
NM_005359.6(SMAD4):c.1529G>T (p.Gly510Val) AND multiple conditions	ClinVar	Detail
NA	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: rs377767371 dbSNP
Genome: hg19
Position: chr18:48,604,707-48,604,707
Variant Type: snv
Reference Allele: G
Alternative Allele: T

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