JAK2 c.1873_1874del ;(p.V625Sfs*17)

Variant ID: 9-5077461-GGT-G

NM_004972.3(JAK2):c.1873_1874del;(p.V625Sfs*17)

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:

Prognostic significance of ASXL1, JAK2V617F mutations and JAK2V617F allele burden in Philadelphia-negative myeloproliferative neoplasms.

Journal Of Blood Medicine
Yonal-Hindilerden, Ipek I; Daglar-Aday, Aynur A; Akadam-Teker, Basak B; Yilmaz, Ceylan C; Nalcaci, Meliha M; Yavuz, Akif Selim AS; Sargin, Deniz D
Publication Date: 2015

Variant appearance in text: JAK2: 1873_1874del
PubMed Link: 26082670
Variant Present in the following documents:
  • Main text
  • jbm-6-157.pdf
View BVdb publication page