DNMT3A c.2194_2195delinsGA ;(p.F732D)

Variant ID: 2-25463298-AA-TC

NM_022552.4(DNMT3A):c.2194_2195delinsGA;(p.F732D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The DNMT3A R882H mutation does not cause dominant negative effects in purified mixed DNMT3A/R882H complexes.

Scientific Reports
Emperle, Max M; Dukatz, Michael M; Kunert, Stefan S; Holzer, Katharina K; Rajavelu, Arumugam A; Jurkowska, Renata Z RZ; Jeltsch, Albert A
Publication Date: 2018-09-05

Variant appearance in text: DNMT3A: F732D
PubMed Link: 30185810
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_31635.pdf
View BVdb publication page