chr18:48604766:C> Detail (hg19) (SMAD4)

Information

Genome

Assembly Position
hg19 chr18:48,604,766-48,604,766
hg38 chr18:51,078,396-51,078,396 

HGVS

Type Transcript Protein
RefSeq NM_005359.5:c.1588delC NP_005350.1:p.His530ThrfsTer7
Ensemble ENST00000588745.5:c.1300delC ENST00000588745.5:p.His434ThrfsTer7
ENST00000398417.6:c.1588delC ENST00000398417.6:p.His530ThrfsTer7
Summary

MGeND

Clinical significance not provided
Variant entry 3
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
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 COSM6980779 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided head of pancreas not provided MGS000040
(TMGS000095)
Hitoshi Nakagama National Cancer Center Japan
not provided bronchus or lung, unspecified not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided head of pancreas not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.588 juvenile polyposis syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
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
rs377767377 dbSNP
Genome
hg19
Position
chr18:48,604,766-48,604,766
Variant Type
snv
Reference Allele
C
Alternative Allele
-
Genome browser