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DNMT3A c.597C>G ;(p.S199R)
Variant ID: 2-25497852-G-C
NM_022552.4(
DNMT3A
):c.597C>G;(p.S199R)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Novel Mutations in a Lethal Case of Lymphomatous Adult T Cell Lymphoma with Cryptic Myocardial Involvement.
Current Oncology (Toronto, Ont.)
Hashemi Zonouz, Taraneh T; Abdulbaki, Rami R; Bandyopadhyay, Bidhan C BC; Nava, Victor E VE
Publication Date: 2021-02-06
Variant appearance in text: DNMT3A: S199R
PubMed Link:
33562071
Variant Present in the following documents:
Main text
curroncol-28-00079.pdf
View BVdb publication page
Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations.
Oncotarget
Porkka, Noora N; Valo, Satu S; Nieminen, Taina T TT; Olkinuora, Alisa A; Mäki-Nevala, Satu S; Eldfors, Samuli S; Peltomäki, Päivi P
Publication Date: 2017-12-08
Variant appearance in text: DNMT3A: S199R
PubMed Link:
29296220
Variant Present in the following documents:
oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page