chr14:77793207:G>T Detail (hg19) (GSTZ1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr14:77,793,207-77,793,207 |
| hg38 | chr14:77,326,864-77,326,864 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_001312660.1:c.94G>T | NP_001299589.1:p.Glu32Ter |
| NM_145870.2:c.94G>T | NP_665877.1:p.Glu32Ter | |
| NM_145871.2:c.94G>T | NP_665878.2:p.Glu32Ter |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | Carcinoma of bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
| <0.001 | Carcinoma of bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
| <0.001 | Malignant neoplasm of urinary bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
| 0.003 | Malignant neoplasm of urinary bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
| Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
| Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
| Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | 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
- rs7975 dbSNP
- Genome
- hg19
- Position
- chr14:77,793,207-77,793,207
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
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