chr19:35154730:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr19:35,645,633-35,660,784 
hg38 chr19:35,154,730-35,169,881

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
0.003 squamous cell carcinoma NA LHGDN Detail
<0.001 Constitutional Symptom NA BeFree Detail
0.003 cystic fibrosis NA BeFree,LHGDN Detail
<0.001 Cytomegalovirus Infections NA BeFree Detail
0.003 Dehydration NA BeFree,LHGDN Detail
<0.001 Graft-vs-Host Disease NA BeFree Detail
<0.001 Leukemia, Myelocytic, Acute NA BeFree Detail
0.003 melanoma NA LHGDN Detail
<0.001 myelofibrosis NA BeFree Detail
0.007 Neoplasm Metastasis NA BeFree,LHGDN Detail
0.003 Pancreatic Neoplasm NA LHGDN Detail
<0.001 seminoma NA BeFree Detail
0.003 Stomach Neoplasms NA LHGDN Detail
<0.001 synovial sarcoma NA BeFree Detail
<0.001 Testicular Neoplasms NA BeFree Detail
<0.001 Tumor Progression NA BeFree Detail
<0.001 Sarcoma, Epithelioid NA BeFree Detail
<0.001 embryonal carcinoma NA BeFree Detail
<0.001 Rhabdoid Tumor NA BeFree Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Liver and Intrahepatic Biliary Tract Carcinoma NA BeFree Detail
<0.001 Malignant neoplasm of liver NA BeFree Detail
<0.001 Malignant neoplasm of pancreas NA BeFree Detail
<0.001 Hematologic Neoplasms We evaluated 688 patients with hematologic malignancies (48% myeloid and 52% lym... BeFree 24907627 Detail
<0.001 Carcinogenesis NA BeFree Detail
<0.001 myelofibrosis In conclusion, a simple model which includes: age, JAK2 V617F-status and constit... BeFree 22280409 Detail
<0.001 breast carcinoma NA BeFree Detail
<0.001 Constitutional Symptom In conclusion, a simple model which includes: age, JAK2 V617F-status and constit... BeFree 22280409 Detail
<0.001 Primary myelofibrosis In conclusion, a simple model which includes: age, JAK2 V617F-status and constit... BeFree 22280409 Detail
<0.001 Morphologically altered structure NA BeFree Detail
<0.001 Distal-Type Epithelioid Sarcoma NA BeFree Detail
<0.001 Proximal-Type Epithelioid Sarcoma NA BeFree Detail
0.003 Mammary Neoplasms NA LHGDN Detail
<0.001 Non-Neoplastic Disorder NA BeFree Detail
<0.001 liver carcinoma NA BeFree Detail
<0.001 Primary myelofibrosis NA BeFree Detail
0.002 Behcet Syndrome NA GAD Detail
<0.001 Malignant neoplasm of breast NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We evaluated 688 patients with hematologic malignancies (48% myeloid and 52% lymphoid) and a median ... DisGeNET Detail
NA DisGeNET Detail
In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can... DisGeNET Detail
NA DisGeNET Detail
In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can... DisGeNET Detail
In conclusion, a simple model which includes: age, JAK2 V617F-status and constitutional symptoms can... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA 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
chr19:35,154,730-35,169,881
Variant Type
snv
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