chr5:135894564:G>A Detail (hg38) (IL9)

Information

Genome

Assembly Position
hg19 chr5:135,230,253-135,230,253 View the variant detail on this assembly version.
hg38 chr5:135,894,564-135,894,564

HGVS

Type Transcript Protein
RefSeq NM_000590.1:c.184-413C>T
Ensemble ENST00000274520.2:c.184-413C>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 146931 OMIM
HGNC 6029 HGNC
Ensembl ENSG00000145839 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv258488200 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Esophageal Neoplasms We conducted a hospital based case-control study to evaluate the genetic effects... BeFree 23886125 Detail
0.005 Esophageal Neoplasms We conducted a hospital based case-control study to evaluate the genetic effects... BeFree 23886125 Detail
<0.001 esophageal carcinoma We conducted a hospital based case-control study to evaluate the genetic effects... BeFree 23886125 Detail
0.008 Malignant neoplasm of esophagus We conducted a hospital based case-control study to evaluate the genetic effects... BeFree 23886125 Detail
Annotation

Annotations

DescrptionSourceLinks
We conducted a hospital based case-control study to evaluate the genetic effects of functional singl... DisGeNET Detail
We conducted a hospital based case-control study to evaluate the genetic effects of functional singl... DisGeNET Detail
We conducted a hospital based case-control study to evaluate the genetic effects of functional singl... DisGeNET Detail
We conducted a hospital based case-control study to evaluate the genetic effects of functional singl... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs31564 dbSNP
Genome
hg38
Position
chr5:135,894,564-135,894,564
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser