chr1:109733932:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr1:110,276,554-110,283,660 
hg38 chr1:109,733,932-109,741,038

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
0.003 squamous cell carcinoma NA BeFree,GAD Detail
0.002 Carcinoma, Transitional Cell NA GAD Detail
<0.001 Malignant tumor of cervix NA BeFree Detail
0.002 Uterine Cervical Neoplasm NA GAD Detail
<0.001 colorectal carcinoma NA BeFree Detail
0.120 Colorectal Neoplasms NA CTD_human Detail
0.002 Coronary heart disease NA GAD Detail
0.002 cystic fibrosis NA GAD Detail
0.002 Deafness NA GAD Detail
0.010 Esophageal Neoplasms NA BeFree,GAD Detail
0.003 Disorder of eye NA BeFree,GAD Detail
0.003 gallbladder neoplasm NA LHGDN Detail
<0.001 glaucoma NA BeFree Detail
<0.001 Glioma NA BeFree Detail
0.002 Hamartoma NA GAD Detail
0.009 Head and Neck Neoplasms NA GAD Detail
0.002 Hearing Loss, Partial NA GAD Detail
<0.001 congenital heart defects NA BeFree Detail
0.002 Hypersensitivity NA GAD Detail
0.008 Hypertensive disease NA BeFree,GAD,LHGDN Detail
0.005 Laryngeal neoplasm NA GAD Detail
0.005 chronic lymphocytic leukemia NA GAD Detail
<0.001 Leukemia, Lymphocytic, Acute, L1 NA BeFree Detail
0.005 Leukoplakia NA BeFree,GAD Detail
<0.001 Leukoplakia, Oral NA BeFree Detail
0.002 Alcoholic Liver Diseases NA GAD Detail
0.005 Liver neoplasms NA GAD Detail
<0.001 Chronic Obstructive Airway Disease NA BeFree Detail
0.002 Lung Neoplasms NA GAD Detail
0.002 Lymphoma, Follicular NA GAD Detail
0.010 Lymphoma, Non-Hodgkin NA BeFree,GAD Detail
0.005 Malignant neoplasm of stomach NA BeFree,GAD Detail
0.002 melanoma NA GAD Detail
<0.001 meningioma NA BeFree Detail
0.002 Mesothelioma NA GAD Detail
0.010 Mouth Neoplasms NA GAD,LHGDN Detail
0.003 Neoplasm Metastasis NA BeFree,GAD Detail
0.002 Neoplasm Recurrence, Local NA GAD Detail
0.002 Neoplasms, Multiple Primary NA GAD Detail
<0.001 osteoporosis NA BeFree Detail
0.002 osteosarcoma NA GAD Detail
0.007 Parkinson disease NA GAD Detail
0.005 Pharyngeal Neoplasms NA GAD Detail
0.002 Pleural Neoplasms NA GAD Detail
0.002 Prenatal Exposure Delayed Effects NA GAD Detail
0.120 Prostatic Neoplasms NA CTD_human Detail
0.002 Respiratory Tract Diseases NA GAD Detail
<0.001 Age-related cataract NA BeFree Detail
0.002 Skin Neoplasms NA GAD Detail
0.002 Carcinoma of lung Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; C... BeFree 17259654 Detail
0.016 Malignant neoplasm of lung Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; C... BeFree 17259654 Detail
0.002 Helicobacter Infections NA GAD Detail
0.002 Neoplasms, Second Primary NA GAD Detail
0.002 Alcohol abuse NA GAD Detail
<0.001 cataract NA BeFree Detail
<0.001 esophageal carcinoma NA BeFree Detail
0.008 Malignant neoplasm of mouth NA BeFree,GAD Detail
<0.001 Malignant neoplasm of oropharynx NA BeFree Detail
<0.001 Malignant neoplasm of pharynx NA BeFree Detail
0.003 Malignant neoplasm of gallbladder NA BeFree,GAD Detail
0.002 Malignant neoplasm of brain NA GAD Detail
<0.001 childhood brain tumor NA BeFree Detail
<0.001 Lip and oral cavity carcinoma NA BeFree Detail
0.002 Ototoxicity NA GAD Detail
<0.001 gallbladder carcinoma NA BeFree Detail
<0.001 Hereditary pancreatitis NA BeFree Detail
<0.001 Bulla of lung NA BeFree Detail
0.016 Malignant neoplasm of lung The smokers with CYP1A1 Msp1 (wt/vt+vt/vt), CYP1A1 exon7 (Val/Val+Ile /Val), GST... BeFree,GAD 25040976 Detail
0.120 Chloracne NA CTD_human Detail
<0.001 Cortical cataract NA BeFree Detail
0.005 Cancer of Head and Neck NA BeFree,GAD Detail
<0.001 laryngeal squamous cell carcinoma NA BeFree Detail
<0.001 cervix carcinoma NA BeFree Detail
0.008 Malignant neoplasm of prostate NA BeFree,GAD Detail
0.008 Malignant neoplasm of esophagus NA BeFree,GAD Detail
<0.001 Carcinoma of larynx NA BeFree Detail
<0.001 Carcinogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 breast carcinoma NA BeFree Detail
0.002 Carcinoma of lung The smokers with CYP1A1 Msp1 (wt/vt+vt/vt), CYP1A1 exon7 (Val/Val+Ile /Val), GST... BeFree 25040976 Detail
0.005 skin carcinoma NA GAD Detail
0.002 Malignant neoplasm of kidney NA GAD Detail
0.120 Drug-Induced Liver Injury NA CTD_human Detail
0.002 Genomic Instability NA GAD Detail
0.002 Malignant neoplasm of ovary NA GAD Detail
0.002 hearing impairment NA GAD Detail
0.017 colorectal cancer NA BeFree,GAD Detail
0.002 Delayed Graft Function NA GAD Detail
<0.001 Meningioma, benign, no ICD-O subtype NA BeFree Detail
0.008 liver carcinoma NA BeFree,GAD,LHGDN Detail
<0.001 Oropharyngeal Carcinoma NA BeFree Detail
0.002 Prostatic Hyperplasia NA GAD Detail
<0.001 Experimental Organism Basal Cell Carcinoma NA BeFree Detail
0.002 Hearing Loss NA GAD Detail
<0.001 adenocarcinoma NA BeFree Detail
0.005 Alzheimer's disease NA BeFree,GAD Detail
0.002 asthma NA GAD Detail
<0.001 Astrocytoma NA BeFree Detail
0.002 atherosclerosis NA GAD Detail
0.007 Malignant neoplasm of urinary bladder NA BeFree,GAD Detail
0.002 Bladder Neoplasm NA GAD Detail
0.008 Malignant neoplasm of breast NA BeFree,GAD Detail
0.003 Malignant neoplasm of larynx NA BeFree,GAD Detail
0.002 basal cell carcinoma NA GAD Detail
<0.001 Bronchogenic Carcinoma NA BeFree Detail
Annotation

Annotations

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Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; CYP2A6 -47A&gt;C; MDR... DisGeNET Detail
Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; CYP2A6 -47A&gt;C; MDR... DisGeNET Detail
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The smokers with CYP1A1 Msp1 (wt/vt+vt/vt), CYP1A1 exon7 (Val/Val+Ile /Val), GSTM1 (-), GSTM3 (AB+BB... DisGeNET Detail
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The smokers with CYP1A1 Msp1 (wt/vt+vt/vt), CYP1A1 exon7 (Val/Val+Ile /Val), GSTM1 (-), GSTM3 (AB+BB... 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
rs386545618 dbSNP
Genome
hg38
Position
chr1:109,733,932-109,741,038
Variant Type
snv
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