chr8:86376236:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr8:86,376,236-86,393,722
hg38 chr8:85,464,007-85,481,493 

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 Carcinoma, Transitional Cell NA BeFree Detail
<0.001 Cardiovascular Diseases NA BeFree Detail
0.080 cholangitis NA CTD_mouse Detail
0.003 ulcerative colitis NA LHGDN Detail
<0.001 Coronary Arteriosclerosis NA BeFree Detail
<0.001 Coronary heart disease NA BeFree Detail
<0.001 cystic fibrosis NA BeFree Detail
<0.001 Dermatitis, Atopic NA BeFree Detail
<0.001 Diabetes Mellitus, Insulin-Dependent NA BeFree Detail
0.003 Down syndrome NA LHGDN Detail
<0.001 Eczema NA BeFree Detail
<0.001 endometriosis NA BeFree Detail
<0.001 Primary myelofibrosis A total of 107 patients with chronic-phase primary myelofibrosis (PMF) were scre... BeFree 22052707 Detail
0.080 Kidney Calculi NA RGD Detail
0.003 Kidney Diseases NA LHGDN Detail
<0.001 Mental Retardation NA BeFree Detail
<0.001 Inborn errors of metabolism NA BeFree Detail
0.003 osteopetrosis NA BeFree Detail
0.122 osteoporosis NA CTD_human,GAD Detail
0.003 Pancreatic Neoplasm NA BeFree,LHGDN Detail
0.003 pancreatitis NA LHGDN Detail
0.003 psoriasis NA BeFree,LHGDN Detail
<0.001 rheumatic heart disease NA BeFree Detail
0.003 schizophrenia NA LHGDN Detail
0.120 Stomach Neoplasms NA CTD_human Detail
<0.001 Encephalopathies NA BeFree Detail
<0.001 acute intermittent porphyria NA BeFree Detail
<0.001 Aortic Aneurysm, Thoracic NA BeFree Detail
<0.001 Neuroectodermal Tumor, Primitive NA BeFree Detail
<0.001 Cystadenocarcinoma, Serous NA BeFree Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Abnormal mental state NA BeFree Detail
0.120 Squamous cell carcinoma of esophagus NA CTD_human Detail
<0.001 extraosseous Ewings sarcoma-primitive neuroepithelial tumor NA BeFree Detail
<0.001 Adenocarcinoma of pancreas NA BeFree Detail
<0.001 Developmental delay (disorder) NA BeFree Detail
<0.001 endometrial carcinoma NA BeFree Detail
<0.001 Oropharynx (excludes nasopharynx) NA BeFree Detail
<0.001 Carotid Atherosclerosis NA BeFree Detail
<0.001 Aqueous Humor Disorders NA BeFree Detail
<0.001 Leukemogenesis NA BeFree Detail
<0.001 Ewings sarcoma-primitive neuroectodermal tumor (PNET) NA BeFree Detail
<0.001 Secondary malignant neoplasm of lymph node NA BeFree Detail
<0.001 Carcinoma of bladder NA BeFree Detail
<0.001 Endothelial dysfunction NA BeFree Detail
<0.001 Atypical teratoid/rhabdoid tumor NA BeFree Detail
<0.001 Mental handicap NA BeFree Detail
<0.001 Non-specific brain syndrome NA BeFree Detail
<0.001 Lattice corneal dystrophy Type I Of the 125 M. tuberculosis isolates, 35 (28%) were found to be rifampicin-resist... BeFree 25526063 Detail
<0.001 Distal renal tubular acidosis NA BeFree Detail
0.001 coronary artery disease NA BeFree Detail
0.121 liver carcinoma NA BeFree,CTD_human Detail
<0.001 Chronic ulcerative colitis NA BeFree Detail
0.001 renal tubular acidosis NA BeFree Detail
0.120 adenocarcinoma NA BeFree,CTD_human Detail
<0.001 adenoma NA BeFree Detail
<0.001 Primary myelofibrosis NA BeFree Detail
<0.001 Alzheimer's disease NA BeFree Detail
<0.001 rheumatoid arthritis NA BeFree Detail
<0.001 beta thalassemia NA BeFree Detail
<0.001 Malignant neoplasm of urinary bladder NA BeFree Detail
<0.001 Metabolic Bone Disorder NA BeFree Detail
0.003 Carcinoid Tumor NA LHGDN Detail
Annotation

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
rs28934572 dbSNP
Genome
hg19
Position
chr8:86,376,236-86,393,722
Variant Type
snv
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