chr9:94178834:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr9:96,941,116-96,941,202 
hg38 chr9:94,178,834-94,178,920

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 Liver Neoplasms, Experimental NA CTD_human Detail
0.120 Precancerous Conditions NA CTD_human Detail
<0.001 Pregnancy Complications NA BeFree Detail
<0.001 pulmonary fibrosis NA BeFree Detail
<0.001 Cancer of Head and Neck NA BeFree Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 Squamous cell carcinoma of the head and neck NA BeFree Detail
<0.001 Idiopathic Pulmonary Fibrosis We further validated six miRNAs (miR-21, miR-199a-5p, miR-200c, miR-31, let-7a, ... BeFree 25725128 Detail
<0.001 Promyelocytic leukemia NA BeFree Detail
<0.001 renal cell carcinoma Our results also demonstrated that Rab25 is a target gene of let-7d, and further... BeFree 25686498 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
We further validated six miRNAs (miR-21, miR-199a-5p, miR-200c, miR-31, let-7a, and let-7d) for furt... DisGeNET Detail
NA DisGeNET Detail
Our results also demonstrated that Rab25 is a target gene of let-7d, and further suggested that Rab2... 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
chr9:94,178,834-94,178,920
Variant Type
snv
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