chr20:23350791:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr20:23,331,428-23,335,408 
hg38 chr20:23,350,791-23,354,771

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 squamous cell carcinoma NA BeFree Detail
<0.001 Carcinoma, Transitional Cell NA BeFree Detail
<0.001 Congenital chromosomal disease NA BeFree Detail
<0.001 colorectal carcinoma NA BeFree Detail
<0.001 Coronary Arteriosclerosis NA BeFree Detail
<0.001 Coronary heart disease NA BeFree Detail
<0.001 Esophageal Neoplasms NA BeFree Detail
0.001 glioblastoma NA BeFree Detail
0.001 Glioma NA BeFree Detail
<0.001 Hepatitis, Chronic NA BeFree Detail
<0.001 hepatitis C NA BeFree Detail
<0.001 HIV Infections NA BeFree Detail
<0.001 keratosis NA BeFree Detail
0.001 leukemia NA BeFree Detail
0.001 chronic lymphocytic leukemia NA BeFree Detail
<0.001 lymphoid leukemia NA BeFree Detail
0.003 Acute lymphocytic leukemia NA BeFree Detail
0.001 Leukemia, Lymphocytic, Acute, L1 NA BeFree Detail
0.004 Leukemia, Myelocytic, Acute NA BeFree Detail
<0.001 myeloid leukemia NA BeFree Detail
<0.001 Myeloid Leukemia, Chronic NA BeFree Detail
<0.001 acute promyelocytic leukemia NA BeFree Detail
<0.001 Leukemia, T-Cell NA BeFree Detail
<0.001 Adult T-Cell Lymphoma/Leukemia NA BeFree Detail
<0.001 Leukoplakia, Oral NA BeFree Detail
<0.001 Lung Neoplasms NA BeFree Detail
0.002 lymphoma NA BeFree Detail
<0.001 Lymphoma, Follicular NA BeFree Detail
<0.001 Malignant neoplasm of stomach Long noncoding RNA PVT1 indicates a poor prognosis of gastric cancer and promote... BeFree 25890171 Detail
0.002 melanoma NA BeFree Detail
<0.001 meningioma NA BeFree Detail
<0.001 Mesothelioma NA BeFree Detail
<0.001 Monosomy NA BeFree Detail
0.002 multiple myeloma However, there is a lack of systematic analysis of p15 epigenetic modification s... BeFree 25382971 Detail
<0.001 Neoplasm Metastasis NA BeFree Detail
<0.001 oligodendroglioma NA BeFree Detail
<0.001 Pancreatic Neoplasm NA BeFree Detail
0.001 retinoblastoma NA BeFree Detail
<0.001 Stomach Neoplasms NA BeFree Detail
<0.001 African Trypanosomiasis NA BeFree Detail
<0.001 B-Cell Lymphomas NA BeFree Detail
<0.001 diffuse large B-cell lymphoma Hypermethylation of p15 gene in diffuse - large B-cell lymphoma: association wit... BeFree 24815848 Detail
<0.001 T-Cell Lymphoma NA BeFree Detail
<0.001 Lymphoma, T-Cell, Cutaneous NA BeFree Detail
0.002 acute leukemia NA BeFree Detail
<0.001 Adenocarcinoma of lung (disorder) NA BeFree Detail
0.001 esophageal carcinoma NA BeFree Detail
0.001 Tumor Progression NA BeFree Detail
<0.001 Follicular thyroid carcinoma NA BeFree Detail
<0.001 Adult Acute Myeloblastic Leukemia NA BeFree Detail
<0.001 uveal melanoma NA BeFree Detail
<0.001 Medullary carcinoma of thyroid NA BeFree Detail
<0.001 Malignant neoplasm of lung NA BeFree Detail
<0.001 Neoplasm, Residual NA BeFree Detail
<0.001 recurrent childhood acute lymphoblastic leukemia NA BeFree Detail
<0.001 T-cell childhood acute lymphoblastic leukemia NA BeFree Detail
<0.001 Solid tumour NA BeFree Detail
<0.001 anaplastic oligodendroglioma NA BeFree Detail
<0.001 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse NA BeFree Detail
<0.001 malignant mesothelioma NA BeFree Detail
<0.001 juvenile myelomonocytic leukemia NA BeFree Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
<0.001 endometrial carcinoma NA BeFree Detail
0.004 Carcinogenesis NA BeFree Detail
0.001 Leukemogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 breast carcinoma NA BeFree Detail
0.001 stomach carcinoma Long noncoding RNA PVT1 indicates a poor prognosis of gastric cancer and promote... BeFree 25890171 Detail
0.001 Carcinoma of bladder NA BeFree Detail
<0.001 Dissecting aneurysm of the thoracic aorta NA BeFree Detail
<0.001 Well Differentiated Oligodendroglioma NA BeFree Detail
<0.001 Invasive breast carcinoma NA BeFree Detail
<0.001 Mycosis fungoides/Sezary syndrome NOS NA BeFree Detail
<0.001 Hyperkeratosis NA BeFree Detail
<0.001 ovarian neoplasm NA BeFree Detail
<0.001 Squamous cell carcinoma of the head and neck NA BeFree Detail
<0.001 Familial multiple trichoepitheliomata NA BeFree Detail
<0.001 Therapy-related myelodysplastic syndrome NA BeFree Detail
<0.001 Hepatocarcinogenesis NA BeFree Detail
<0.001 colorectal cancer NA BeFree Detail
<0.001 Glioblastoma multiforme NA BeFree Detail
<0.001 MULTICYSTIC RENAL DYSPLASIA, BILATERAL NA BeFree Detail
<0.001 coronary artery disease NA BeFree Detail
<0.001 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma NA BeFree Detail
0.002 Precursor Cell Lymphoblastic Leukemia Lymphoma NA BeFree Detail
0.002 liver carcinoma NA BeFree Detail
<0.001 adenoma NA BeFree Detail
<0.001 Primary myelofibrosis NA BeFree Detail
<0.001 Astrocytoma NA BeFree Detail
0.001 Malignant neoplasm of urinary bladder NA BeFree Detail
0.001 Bladder Neoplasm NA BeFree Detail
<0.001 Blast Phase NA BeFree Detail
<0.001 Brain Neoplasms NA BeFree Detail
<0.001 Malignant neoplasm of breast NA BeFree Detail
<0.001 Non-small cell lung carcinoma NA BeFree Detail
Annotation

Annotations

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Long noncoding RNA PVT1 indicates a poor prognosis of gastric cancer and promotes cell proliferation... DisGeNET Detail
NA DisGeNET Detail
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However, there is a lack of systematic analysis of p15 epigenetic modification such as methylation i... DisGeNET Detail
NA DisGeNET Detail
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Hypermethylation of p15 gene in diffuse - large B-cell lymphoma: association with less aggressivenes... DisGeNET Detail
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Long noncoding RNA PVT1 indicates a poor prognosis of gastric cancer and promotes cell proliferation... 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
-
Genome
hg38
Position
chr20:23,350,791-23,354,771
Variant Type
snv
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