chr10:106039185:A>G Detail (hg19) (GSTO2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr10:106,039,185-106,039,185 |
hg38 | chr10:104,279,427-104,279,427 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001191013.1:c.366+1311A>G | |
NM_183239.1:c.424A>G | NP_899062.1:p.Asn142Asp | |
NM_001191014.1:c.340A>G | NP_001177943.1:p.Asn114Asp |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:0.279 |
ToMMo:0.271 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.239 |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
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 | Malignant neoplasm of urinary bladder | To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs1566... | BeFree | 25716313 | Detail |
<0.001 | Carcinoma of bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
<0.001 | Carcinoma of bladder | To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs1566... | BeFree | 25716313 | Detail |
<0.001 | Carcinoma of bladder | To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs1566... | BeFree | 25716313 | Detail |
<0.001 | Malignant neoplasm of urinary bladder | To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs1566... | BeFree | 25716313 | Detail |
0.005 | Malignant neoplasm of urinary bladder | To examine the association of six glutathione transferase (GST) gene polymorphis... | BeFree | 24040330 | Detail |
<0.001 | Carcinoma of bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
0.003 | colorectal cancer | Association between N142D genetic polymorphism of GSTO2 and susceptibility to co... | BeFree | 21113667 | Detail |
<0.001 | Malignant neoplasm of urinary bladder | Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... | BeFree | 22306368 | Detail |
0.004 | Carcinoma of bladder | To examine the association of six glutathione transferase (GST) gene polymorphis... | BeFree | 24040330 | 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 |
---|---|---|
To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs156697) in individual su... | DisGeNET | Detail |
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs156697) in individual su... | DisGeNET | Detail |
To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs156697) in individual su... | DisGeNET | Detail |
To clarify the role of genetic polymorphisms of GSTO1 (rs4925) and GSTO2 (rs156697) in individual su... | DisGeNET | Detail |
To examine the association of six glutathione transferase (GST) gene polymorphisms (GSTT1, GSTP1/rs1... | DisGeNET | Detail |
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
Association between N142D genetic polymorphism of GSTO2 and susceptibility to colorectal cancer. | DisGeNET | Detail |
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... | DisGeNET | Detail |
To examine the association of six glutathione transferase (GST) gene polymorphisms (GSTT1, GSTP1/rs1... | 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
- -
- Genome
- hg19
- Position
- chr10:106,039,185-106,039,185
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- Filtering Status (HGVD)
- PASS
- # of samples (HGVD)
- 1200
- Mean of sample read depth (HGVD)
- 67.22
- Standard deviation of sample read depth (HGVD)
- 30.94
- Number of reference allele (HGVD)
- 1731
- Number of alternative allele (HGVD)
- 669
- Allele Frequency (HGVD)
- 0.27875
- Gene Symbol (HGVD)
- GSTO2
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs156697
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2709
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 4540
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8636
- East Asian Allele Counts (ExAC)
- 2063
- East Asian Heterozygous Counts (ExAC)
- 1533
- East Asian Homozygous Counts (ExAC)
- 265
- East Asian Allele Frequency (ExAC)
- 0.2388837424733673
- Chromosome Counts in All Race (ExAC)
- 121314
- Allele Counts in All Race (ExAC)
- 43210
- Heterozygous Counts in All Race (ExAC)
- 25644
- Homozygous Counts in All Race (ExAC)
- 8783
- Allele Frequency in All Race (ExAC)
- 0.35618312808084807
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