chr21:33266367:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr21:34,638,672-34,683,725 
hg38 chr21:33,266,367-33,311,420

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
0.120 brain ischemia NA CTD_human Detail
<0.001 colitis NA BeFree Detail
<0.001 ulcerative colitis NA BeFree Detail
0.002 Connective Tissue Diseases NA GAD Detail
<0.001 Crohn Disease NA BeFree Detail
0.121 Down syndrome NA BeFree,CTD_human Detail
<0.001 Enterocolitis NA BeFree Detail
0.002 Fetal Diseases NA GAD Detail
0.005 Graft-vs-Host Disease NA BeFree,GAD Detail
0.121 hepatitis B NA BeFree,CTD_human Detail
<0.001 hepatitis C NA BeFree Detail
0.002 HIV Infections NA GAD Detail
0.002 Hyperparathyroidism, Secondary NA GAD Detail
0.005 Inflammation NA GAD Detail
<0.001 Inflammatory Bowel Diseases NA BeFree Detail
<0.001 leprosy NA BeFree Detail
<0.001 Liver diseases NA BeFree Detail
<0.001 Lupus Erythematosus, Systemic NA BeFree Detail
0.003 measles NA BeFree,GAD Detail
0.002 multiple myeloma NA GAD Detail
0.002 mumps NA GAD Detail
0.002 Musculoskeletal Diseases NA GAD Detail
0.002 Pregnancy Complications, Hematologic NA GAD Detail
0.002 Respiratory Syncytial Virus Infections NA GAD Detail
0.003 rubella NA BeFree,GAD Detail
0.002 Dermatologic disorders NA GAD Detail
<0.001 Virus Diseases NA BeFree Detail
<0.001 B-Cell Lymphomas NA BeFree Detail
<0.001 diffuse large B-cell lymphoma Gene expression of IL10, IL10RA and IL10RB was markedly elevated in DLBCLs. BeFree 25733167 Detail
0.002 bacterial vaginosis NA GAD Detail
0.009 Premature Birth NA GAD Detail
0.120 Muscle Weakness NA CTD_human Detail
<0.001 Ki-1+ Anaplastic Large Cell Lymphoma NA BeFree Detail
0.005 Malignant neoplasm of lung NA GAD Detail
0.121 hepatitis B Furthermore, AA genotype of IL10RB-K47E was found to be significantly decreased ... BeFree 23745570 Detail
0.080 Necrotizing Enterocolitis NA RGD Detail
0.003 Hepatitis B, Chronic NA BeFree,GAD Detail
<0.001 Acute GVH disease NA BeFree Detail
0.002 diffuse scleroderma NA GAD Detail
<0.001 Tumor Immunity Our results suggest that mutations that disrupt the interactions of IL-10 with i... BeFree 25056661 Detail
<0.001 liver carcinoma NA BeFree Detail
0.002 Infection NA GAD Detail
<0.001 rheumatoid arthritis NA BeFree Detail
0.002 asthma NA GAD Detail
0.002 Bronchiolitis, Viral NA GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Gene expression of IL10, IL10RA and IL10RB was markedly elevated in DLBCLs. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Furthermore, AA genotype of IL10RB-K47E was found to be significantly decreased in chronic HBV patie... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our results suggest that mutations that disrupt the interactions of IL-10 with its receptors (IL-10R... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA 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
-
dbSNP
rs386574522 dbSNP
Genome
hg38
Position
chr21:33,266,367-33,311,420
Variant Type
snv
Genome browser