chr11:4704784:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr11:4,726,014-5,013,661 
hg38 chr11:4,704,784-4,992,431

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 LHGDN Detail
0.002 Coronary heart disease NA GAD Detail
0.003 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree,GAD Detail
<0.001 Endometrial Neoplasms NA BeFree Detail
<0.001 endometrial hyperplasia NA BeFree Detail
0.002 Mucocutaneous Lymph Node Syndrome NA GAD Detail
<0.001 Neoplasm Metastasis NA BeFree Detail
<0.001 Ovarian Diseases NA BeFree Detail
0.003 Pancreatic Neoplasm NA LHGDN Detail
0.003 polycystic ovary syndrome NA LHGDN Detail
0.003 Prostatic Neoplasms NA BeFree,LHGDN Detail
<0.001 prostatitis NA BeFree Detail
0.121 Dermatologic disorders NA BeFree,CTD_human Detail
0.003 Uterine hemorrhage NA LHGDN Detail
0.001 Tumor Progression NA BeFree Detail
<0.001 verrucous carcinoma NA BeFree Detail
<0.001 Squamous cell carcinoma of esophagus NA BeFree Detail
0.003 Prostatic Intraepithelial Neoplasias NA LHGDN Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
<0.001 endometrial carcinoma NA BeFree Detail
<0.001 Carcinogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 invasive cancer NA BeFree Detail
<0.001 breast carcinoma NA BeFree Detail
<0.001 Carcinoma of lung NA BeFree Detail
<0.001 Malignant Squamous Cell Neoplasm NA BeFree Detail
0.002 Malignant neoplasm of ovary NA GAD Detail
<0.001 High-Grade Prostatic Intraepithelial Neoplasia NA BeFree Detail
<0.001 Epithelioma NA BeFree Detail
0.005 Mammary Neoplasms NA LHGDN Detail
<0.001 Skin Carcinogenesis NA BeFree Detail
<0.001 Non-Neoplastic Disorder NA BeFree Detail
<0.001 uterine corpus cancer NA BeFree Detail
<0.001 liver carcinoma Our study thus highlights the FGFR2 signaling pathway and MMP7 and MMP26 as nove... BeFree 25091573 Detail
0.120 Spontaneous abortion NA CTD_human Detail
<0.001 Anaplasia NA BeFree Detail
<0.001 Malignant neoplasm of breast NA BeFree Detail
<0.001 Malignant neoplasm of endometrium NA BeFree Detail
<0.001 Merkel cell carcinoma NA BeFree Detail
<0.001 Non-small cell lung carcinoma Our study thus highlights FGFR signaling pathway and MMP26 as novel therapeutic ... BeFree 25566961 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
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our study thus highlights the FGFR2 signaling pathway and MMP7 and MMP26 as novel therapeutic target... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our study thus highlights FGFR signaling pathway and MMP26 as novel therapeutic targets for NSCLC th... 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
-
Genome
hg38
Position
chr11:4,704,784-4,992,431
Variant Type
snv
Genome browser