chr18:51058458:>CCTGTTCACAATGAGCTTGCATTCCAGCCTCCCATTTCCAAG Detail (hg38) (SMAD4)

Information

Genome

Assembly Position
hg19 chr18:48,584,828-48,584,828 
hg38 chr18:51,058,458-51,058,458

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.122 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs771084683 dbSNP
Genome
hg38
Position
chr18:51,058,458-51,058,458
Variant Type
snv
Reference Allele
-
Alternative Allele
CCTGTTCACAATGAGCTTGCATTCCAGCCTCCCATTTCCAAG
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