DNMT3A c.2662del ;(p.L888Cfs*18)

Variant ID: 2-25457225-AG-A

NM_022552.4(DNMT3A):c.2662del;(p.L888Cfs*18)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The significance of genetic mutations and their prognostic impact on patients with incidental finding of isolated del(20q) in bone marrow without morphologic evidence of a myeloid neoplasm.

Blood Cancer Journal
Ravindran, Aishwarya A; He, Rong R; Ketterling, Rhett P RP; Jawad, Majd D MD; Chen, Dong D; Oliveira, Jennifer L JL; Nguyen, Phuong L PL; Viswanatha, David S DS; Reichard, Kaaren K KK; Hoyer, James D JD; Go, Ronald S RS; Shi, Min M
Publication Date: 2020-01-23

Variant appearance in text: DNMT3A: 2662del; Leu888Cysfs*18
PubMed Link: 31974359
Variant Present in the following documents:
  • Main text
  • 41408_2020_Article_275.pdf
View BVdb publication page