chr11:67352689:A>T Detail (hg19) (GSTP1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr11:67,352,689-67,352,689 |
| hg38 | chr11:67,585,218-67,585,218 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
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
- -
- Genome
- hg19
- Position
- chr11:67,352,689-67,352,689
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- T
- MMMP State (molecule) (MMMP)
- polymorphism rs1695
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