chr20:62136733:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr20:60,711,789-60,718,486 
hg38 chr20:62,136,733-62,143,430

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 carcinoma NA BeFree Detail
0.003 Colorectal Neoplasms NA LHGDN Detail
<0.001 HIV Infections NA BeFree Detail
<0.001 Virus Diseases NA BeFree Detail
<0.001 Monocytosis NA BeFree Detail
<0.001 Secondary malignant neoplasm of liver NA BeFree Detail
<0.001 Xenograft Model In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myelopro... BeFree 25479752 Detail
<0.001 Myeloproliferative disease In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myelopro... BeFree 25479752 Detail
<0.001 Chronic myeloproliferative disorder In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myelopro... BeFree 25479752 Detail
<0.001 colorectal cancer NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm ... DisGeNET Detail
In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm ... DisGeNET Detail
In mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm ... DisGeNET Detail
NA 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
-
dbSNP
rs386626619 dbSNP
Genome
hg38
Position
chr20:62,136,733-62,143,430
Variant Type
snv
Genome browser