chr21:35720715:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr21:37,093,013-37,093,106 
hg38 chr21:35,720,715-35,720,808

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 Down syndrome NA BeFree Detail
<0.001 obesity NA BeFree Detail
<0.001 pancreatic carcinoma Overexpression of miR-802 in MiaPaCa pancreatic cancer cells reduced TCF4 protei... BeFree 25910082 Detail
<0.001 Malignant neoplasm of lung The results of the quantitative polymerase chain reaction revealed that expressi... BeFree 24994111 Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 Malignant neoplasm of pancreas Overexpression of miR-802 in MiaPaCa pancreatic cancer cells reduced TCF4 protei... BeFree 25910082 Detail
<0.001 Carcinoma of lung microRNA‑802 promotes lung carcinoma proliferation by targeting the tumor suppre... BeFree 24994111 Detail
<0.001 DOWN SYNDROME CRITICAL REGION NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
Overexpression of miR-802 in MiaPaCa pancreatic cancer cells reduced TCF4 protein levels. DisGeNET Detail
The results of the quantitative polymerase chain reaction revealed that expression levels of miR‑802... DisGeNET Detail
NA DisGeNET Detail
Overexpression of miR-802 in MiaPaCa pancreatic cancer cells reduced TCF4 protein levels. DisGeNET Detail
microRNA‑802 promotes lung carcinoma proliferation by targeting the tumor suppressor menin. 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
-
Genome
hg38
Position
chr21:35,720,715-35,720,808
Variant Type
snv
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