Bibliome.ai browser hg19
Search
About
Stats
FAQ
DNMT3A c.2260C>T ;(p.L754F)
Variant ID: 2-25463233-G-A
NM_022552.4(
DNMT3A
):c.2260C>T;(p.L754F)
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:
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
Genome Medicine
Cao, Ye Y; Tokita, Mari J MJ; Chen, Edward S ES; Ghosh, Rajarshi R; Chen, Tiansheng T; Feng, Yanming Y; Gorman, Elizabeth E; Gibellini, Federica F; Ward, Patricia A PA; Braxton, Alicia A; Wang, Xia X; Meng, Linyan L; Xiao, Rui R; Bi, Weimin W; Xia, Fan F; Eng, Christine M CM; Yang, Yaping Y; Gambin, Tomasz T; Shaw, Chad C; Liu, Pengfei P; Stankiewicz, Pawel P
Publication Date: 2019-07-26
Variant appearance in text: DNMT3A: 2260C>T; L754F
PubMed Link:
31349857
Variant Present in the following documents:
Main text
13073_2019_658_MOESM4_ESM.xlsx, sheet 1
13073_2019_Article_658.pdf
View BVdb publication page