chr9:131857073:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr9:131,857,073-131,873,072
hg38 chr9:129,094,794-129,110,793 

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
Score Disease name Description Source Pubmed Links
<0.001 squamous cell carcinoma NA BeFree Detail
<0.001 Malignant tumor of cervix NA BeFree Detail
<0.001 Uterine Cervical Neoplasm NA BeFree Detail
<0.001 cholesterol ester storage disease NA BeFree Detail
<0.001 choriocarcinoma NA BeFree Detail
<0.001 Congenital chromosomal disease This study was conducted to determine the association between arsenic exposure a... BeFree 25395496 Detail
<0.001 Cockayne syndrome NA BeFree Detail
<0.001 colorectal carcinoma NA BeFree Detail
<0.001 cutis laxa NA BeFree Detail
<0.001 Dental Plaque NA BeFree Detail
<0.001 Diabetes Mellitus, Insulin-Dependent NA BeFree Detail
<0.001 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree Detail
<0.001 Diabetic Nephropathy NA BeFree Detail
<0.001 Elliptocytosis, Hereditary NA BeFree Detail
<0.001 fragile X syndrome NA BeFree Detail
<0.001 cardiac arrest NA BeFree Detail
<0.001 congestive heart failure NA BeFree Detail
<0.001 hepatitis B NA BeFree Detail
<0.001 Hepatolenticular Degeneration Variability within the CAT gene may be an important modifier of the clinical cou... BeFree 24517502 Detail
<0.001 Herpes Simplex Infections NA BeFree Detail
0.006 HIV Infections NA BeFree Detail
<0.001 male infertility Human catalase gene polymorphism (CAT C-262T) and risk of male infertility. BeFree 24456074 Detail
<0.001 influenza NA BeFree Detail
<0.001 insulinoma NA BeFree Detail
<0.001 kernicterus NA BeFree Detail
<0.001 Adult T-Cell Lymphoma/Leukemia NA BeFree Detail
<0.001 Leukoencephalopathy, Progressive Multifocal NA BeFree Detail
0.004 Liver neoplasms NA BeFree Detail
<0.001 Chronic Obstructive Airway Disease NA BeFree Detail
<0.001 Lupus Erythematosus, Systemic NA BeFree Detail
<0.001 lymphoma NA BeFree Detail
<0.001 Lymphoma, Non-Hodgkin For the TYMS gene, haplotype CAT at TYMS (OR 0.67, 95% CI 0.49-0.90, P = 0.007) ... BeFree 25384508 Detail
<0.001 melanoma NA BeFree Detail
<0.001 Mental Retardation NA BeFree Detail
<0.001 Monosomy NA BeFree Detail
0.002 narcolepsy NA GAD Detail
<0.001 Neoplasm Metastasis NA BeFree Detail
<0.001 nephroblastoma NA BeFree Detail
0.001 neuroblastoma NA BeFree Detail
<0.001 Degenerative polyarthritis NA BeFree Detail
<0.001 osteosarcoma NA BeFree Detail
<0.001 ovarian carcinoma NA BeFree Detail
<0.001 Parkinson disease NA BeFree Detail
<0.001 pheochromocytoma NA BeFree Detail
<0.001 Pituitary Diseases NA BeFree Detail
<0.001 Pituitary Neoplasms NA BeFree Detail
<0.001 plasmacytoma NA BeFree Detail
<0.001 Superinfection NA BeFree Detail
<0.001 Tuberculosis, Pulmonary NA BeFree Detail
<0.001 Vascular Diseases NA BeFree Detail
<0.001 vitiligo NA BeFree Detail
<0.001 xeroderma pigmentosum NA BeFree Detail
<0.001 Hallopeau-Siemens Disease NA BeFree Detail
<0.001 eosinophilia-myalgia syndrome NA BeFree Detail
<0.001 Ataxia, Spinocerebellar NA BeFree Detail
<0.001 Small cell carcinoma of lung NA BeFree Detail
<0.001 Aortic Aneurysm, Thoracic NA BeFree Detail
0.001 hepatoblastoma NA BeFree Detail
<0.001 embryonal carcinoma NA BeFree Detail
<0.001 teratocarcinoma NA BeFree Detail
<0.001 Follicular thyroid carcinoma NA BeFree Detail
<0.001 Extrapyramidal sign NA BeFree Detail
<0.001 Cerebral atrophy NA BeFree Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Anaplastic thyroid carcinoma NA BeFree Detail
<0.001 Medullary carcinoma of thyroid NA BeFree Detail
<0.001 Papillary thyroid carcinoma NA BeFree Detail
<0.001 Malignant neoplasm of lung NA BeFree Detail
<0.001 Chronic Periodontitis NA BeFree Detail
<0.001 Spastic syndrome NA BeFree Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 cervix carcinoma NA BeFree Detail
<0.001 Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site NA BeFree Detail
0.002 Malignant neoplasm of prostate This study of advanced prostate cancer risk showed a marginal association with a... BeFree 25315963 Detail
<0.001 endometrial carcinoma NA BeFree Detail
<0.001 Overweight NA BeFree Detail
<0.001 Metabolic syndrome X NA BeFree Detail
<0.001 Thyroid carcinoma NA BeFree Detail
<0.001 lymphoma Data from two population-based, case-control studies of lymphoma in the UK (700 ... BeFree 16956821 Detail
<0.001 Osteosarcoma of bone NA BeFree Detail
0.002 prostate carcinoma This study of advanced prostate cancer risk showed a marginal association with a... BeFree 25315963 Detail
0.004 breast carcinoma NA BeFree Detail
<0.001 Carcinoma of lung NA BeFree Detail
<0.001 colon carcinoma NA BeFree Detail
0.001 Central neuroblastoma NA BeFree Detail
0.001 spinocerebellar ataxia type 1 NA BeFree Detail
<0.001 latent infection NA BeFree Detail
<0.001 Malignant neoplasm of ovary NA BeFree Detail
<0.001 Squamous cell carcinoma of the head and neck NA BeFree Detail
<0.001 Ductal Carcinoma NA BeFree Detail
<0.001 diffuse scleroderma NA BeFree Detail
0.001 Mammary Neoplasms NA BeFree Detail
<0.001 colorectal cancer NA BeFree Detail
<0.001 Ductal Breast Carcinoma NA BeFree Detail
0.002 Glomerular filtration rate finding NA GAD Detail
<0.001 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) NA BeFree Detail
<0.001 Amyotrophic Lateral Sclerosis, Sporadic NA BeFree Detail
0.005 liver carcinoma In accordance, haplotypic analysis of the three polymorphisms also showed that t... BeFree 24867713 Detail
<0.001 adenoma NA BeFree Detail
<0.001 Alcoholic Intoxication, Chronic Our findings suggest that the CAT c.-262C>T genetic polymorphism influences the ... BeFree 25514903 Detail
<0.001 amyotrophic lateral sclerosis NA BeFree Detail
<0.001 Refractory anaemia with excess blasts NA BeFree Detail
<0.001 Anxiety Disorders Our findings suggest that the CAT c.-262C>T genetic polymorphism influences the ... BeFree 25514903 Detail
0.001 asthma NA BeFree Detail
<0.001 Barrett esophagus BOB CAT: A Large-Scale Review and Delphi Consensus for Management of Barrett's E... BeFree 25869390 Detail
<0.001 bipolar disorder NA BeFree Detail
0.004 Malignant neoplasm of breast NA BeFree Detail
<0.001 Malignant tumor of colon NA BeFree Detail
<0.001 Malignant neoplasm of thyroid NA BeFree Detail
<0.001 Non-small cell lung carcinoma NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
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This study was conducted to determine the association between arsenic exposure and polymorphisms of ... DisGeNET Detail
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Variability within the CAT gene may be an important modifier of the clinical course of WD. DisGeNET Detail
NA DisGeNET Detail
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Human catalase gene polymorphism (CAT C-262T) and risk of male infertility. DisGeNET Detail
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For the TYMS gene, haplotype CAT at TYMS (OR 0.67, 95% CI 0.49-0.90, P = 0.007) was associated with ... DisGeNET Detail
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This study of advanced prostate cancer risk showed a marginal association with a CAT polymorphism an... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 contro... DisGeNET Detail
NA DisGeNET Detail
This study of advanced prostate cancer risk showed a marginal association with a CAT polymorphism an... DisGeNET Detail
NA DisGeNET Detail
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In accordance, haplotypic analysis of the three polymorphisms also showed that the haplotype block C... DisGeNET Detail
NA DisGeNET Detail
Our findings suggest that the CAT c.-262C>T genetic polymorphism influences the susceptibility to al... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our findings suggest that the CAT c.-262C>T genetic polymorphism influences the susceptibility to al... DisGeNET Detail
NA DisGeNET Detail
BOB CAT: A Large-Scale Review and Delphi Consensus for Management of Barrett's Esophagus With No Dys... DisGeNET Detail
NA DisGeNET Detail
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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
rs386596107 dbSNP
Genome
hg19
Position
chr9:131,857,073-131,873,072
Variant Type
snv
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