chr15:45023147:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr15:45,315,345-45,369,383 
hg38 chr15:45,023,147-45,077,185

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 Colorectal Neoplasms NA BeFree Detail
<0.001 Congenital cataract NA BeFree Detail
<0.001 Diabetes NA BeFree Detail
<0.001 diabetes mellitus NA BeFree Detail
0.080 Diabetes Mellitus, Experimental NA RGD Detail
<0.001 diabetic cataract NA BeFree Detail
<0.001 Diabetic Nephropathy NA BeFree Detail
<0.001 diabetic retinopathy NA BeFree Detail
<0.001 Kidney Diseases NA BeFree Detail
0.200 Myocardial Reperfusion Injury NA CTD_human,RGD Detail
<0.001 cataract NA BeFree Detail
<0.001 Hepatic necrosis NA BeFree Detail
0.120 Necrotizing Enterocolitis NA CTD_human Detail
<0.001 Bilateral cataracts (disorder) NA BeFree Detail
0.002 Malignant neoplasm of ovary NA GAD Detail
<0.001 TUBEROUS SCLEROSIS 1 (disorder) NA BeFree Detail
<0.001 adenoma 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
hg38
Position
chr15:45,023,147-45,077,185
Variant Type
snv
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