chr18:48591977:G>A Detail (hg19) (SMAD4)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr18:48,591,977-48,591,977 |
hg38 | chr18:51,065,607-51,065,607 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005359.5:c.1139+1G>A | |
Ensemble | ENST00000342988.8:c.1139+1G>A | |
ENST00000398417.6:c.1139+1G>A |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
![]() |
Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
2021-09-07 | criteria provided, single submitter | juvenile polyposis syndrome |
![]() |
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.1139+1G>A AND Juvenile polyposis syndrome | ClinVar | Detail |
NA | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs377767354 dbSNP
- Genome
- hg19
- Position
- chr18:48,591,977-48,591,977
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser