chr4:86911160:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr4:86,911,160-87,515,778
hg38 chr4:85,990,007-86,594,625 

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 Cognition Disorders NA BeFree Detail
0.002 HIV Infections NA GAD Detail
<0.001 ovarian carcinoma NA BeFree Detail
<0.001 Seizures NA BeFree Detail
0.120 Lennox-Gastaut syndrome NA ORPHANET Detail
<0.001 Ovarian epithelial cancer stage II NA BeFree Detail
<0.001 Epileptic encephalopathy NA BeFree Detail
<0.001 Epithelial ovarian cancer NA BeFree Detail
<0.001 Malignant neoplasm of ovary NA BeFree Detail
<0.001 Squamous cell carcinoma of the head and neck NA BeFree Detail
0.120 Epileptic encephalopathy, Lennox-Gastaut type NA CTD_human Detail
<0.001 intellectual disability NA BeFree Detail
<0.001 Brain Diseases NA BeFree Detail
<0.001 Brain Neoplasms NA BeFree Detail
Annotation

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
hg19
Position
chr4:86,911,160-87,515,778
Variant Type
snv
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