JAK2 c.171T>A ;(p.F57L)

Variant ID: 9-5022158-T-A

NM_004972.3(JAK2):c.171T>A;(p.F57L)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Integration Analysis of JAK2 or RUNX1 Mutation With Bone Marrow Blast Can Improve Risk Stratification in the Patients With Lower Risk Myelodysplastic Syndrome.

Frontiers In Oncology
Fang, Ying Y; Guo, Juan J; Wu, Dong D; Wu, Ling-Yun LY; Song, Lu-Xi LX; Zhang, Zheng Z; Zhao, You-Shan YS; Chang, Chun-Kang CK
Publication Date: 2020

Variant appearance in text: JAK2: F57L
PubMed Link: 33520721
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page