Bibliome.ai browser hg19
Search
About
Stats
FAQ
JAK2 c.2719C>A ;(p.H907N)
Variant ID: 9-5089821-C-A
NM_004972.3(
JAK2
):c.2719C>A;(p.H907N)
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: H907N
PubMed Link:
33520721
Variant Present in the following documents:
Table_2.xlsx, sheet 1
View BVdb publication page