chr9:97687210:T>G Detail (hg38) (XPA)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr9:100,449,492-100,449,492 View the variant detail on this assembly version. |
hg38 | chr9:97,687,210-97,687,210 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000380.3:c.441A>C | NP_000371.1:p.Glu147Asp |
Ensemble | ENST00000375128.5:c.441A>C | ENST00000375128.5:p.Glu147Asp |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
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 |
---|---|---|---|---|---|
0.007 | Malignant neoplasm of stomach | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.002 | stomach carcinoma | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.006 | stomach carcinoma | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.009 | stomach carcinoma | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
<0.001 | Paroxysmal atrial tachycardia | We investigated the association of 10 base-excision and nucleotide-excision repa... | BeFree | 17531525 | Detail |
0.013 | Malignant neoplasm of stomach | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.003 | stomach carcinoma | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.010 | Malignant neoplasm of stomach | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.005 | stomach carcinoma | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.012 | Malignant neoplasm of stomach | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.003 | Carcinoma of lung | We investigated the association of 10 base-excision and nucleotide-excision repa... | BeFree | 17531525 | Detail |
0.036 | Malignant neoplasm of lung | We investigated the association of 10 base-excision and nucleotide-excision repa... | BeFree | 17531525 | Detail |
0.007 | Malignant neoplasm of stomach | Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R39... | BeFree | 20817763 | Detail |
0.084 | Carcinoma of lung | We investigated the association of 10 base-excision and nucleotide-excision repa... | BeFree | 17531525 | Detail |
0.044 | Malignant neoplasm of lung | We investigated the association of 10 base-excision and nucleotide-excision repa... | BeFree | 17531525 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphism... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphism... | DisGeNET | Detail |
We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphism... | DisGeNET | Detail |
Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), ... | DisGeNET | Detail |
We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphism... | DisGeNET | Detail |
We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphism... | 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
- hg38
- Position
- chr9:97,687,210-97,687,210
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- G
- East Asian Chromosome Counts (ExAC)
- 8600
- East Asian Allele Counts (ExAC)
- 0
- East Asian Heterozygous Counts (ExAC)
- 0
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.0
- Chromosome Counts in All Race (ExAC)
- 120382
- Allele Counts in All Race (ExAC)
- 2
- Heterozygous Counts in All Race (ExAC)
- 2
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 1.6613779468691332E-5
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