chr6:100836232:>A Detail (hg19) (SIM1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr6:100,836,232-100,836,232 |
| hg38 | chr6:100,388,356-100,388,356 |
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
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| A nominal evidence of association was found for the nonsynonymous variant P352T C/A (rs3734354) (P =... | 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
- rs35180395 dbSNP
- Genome
- hg19
- Position
- chr6:100,836,232-100,836,232
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- A
Genome browser