chr4:101316498:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr4:101,316,498-101,439,179
hg38 chr4:100,395,341-100,518,022 

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 Dermatitis, Atopic NA BeFree Detail
<0.001 Eczema NA BeFree Detail
<0.001 hemangioma NA BeFree Detail
<0.001 Hemangiosarcoma NA BeFree Detail
<0.001 Acute lymphocytic leukemia NA BeFree Detail
<0.001 Dermatologic disorders NA BeFree Detail
0.002 Tobacco use disorder NA GAD Detail
<0.001 T-Cell Lymphoma NA BeFree Detail
<0.001 sarcoma NA BeFree Detail
<0.001 Precursor Cell Lymphoblastic Leukemia Lymphoma NA BeFree Detail
<0.001 rheumatoid arthritis 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
chr4:101,316,498-101,439,179
Variant Type
snv
Genome browser