chr18:51067072:G>A Detail (hg38) (SMAD4)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr18:48,593,442-48,593,442 View the variant detail on this assembly version. |
hg38 | chr18:51,067,072-51,067,072 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005359.5:c.1193G>A | NP_005350.1:p.Trp398Ter |
Ensemble | ENST00000342988.8:c.1193G>A | ENST00000342988.8:p.Trp398Ter |
ENST00000398417.6:c.1193G>A | ENST00000398417.6:p.Trp398Ter |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2023-07-31 | criteria provided, single submitter | juvenile polyposis syndrome |
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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.1193G>A (p.Trp398Ter) AND Juvenile polyposis syndrome | 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
- rs377767357 dbSNP
- Genome
- hg38
- Position
- chr18:51,067,072-51,067,072
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser