chr16:1290380:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr16:1,290,380-1,292,555
hg38 chr16:1,240,379-1,242,554 

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 contact dermatitis NA CTD_human Detail
0.003 fibrosarcoma NA LHGDN Detail
0.002 Hypersensitivity NA GAD Detail
0.005 Inflammation NA LHGDN Detail
0.005 mastocytosis NA GAD,LHGDN Detail
0.003 multiple sclerosis NA LHGDN Detail
0.003 Degenerative polyarthritis NA LHGDN Detail
0.003 rheumatoid arthritis NA LHGDN Detail
0.003 asthma NA LHGDN 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
chr16:1,290,380-1,292,555
Variant Type
snv
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