Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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