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HR c.2324_2325delinsAT ;(p.R775H)
Variant ID: 8-21978620-TC-AT
NM_005144.4(
HR
):c.2324_2325delinsAT;(p.R775H)
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:
Target amplicon exome-sequencing identifies promising diagnosis and prognostic markers involved in RTK-RAS and PI3K-AKT signaling as central oncopathways in primary central nervous system lymphoma.
Oncotarget
Takashima, Yasuo Y; Sasaki, Yasushi Y; Hayano, Azusa A; Homma, Jumpei J; Fukai, Junya J; Iwadate, Yasuo Y; Kajiwara, Koji K; Ishizawa, Shin S; Hondoh, Hiroaki H; Tokino, Takashi T; Yamanaka, Ryuya R
Publication Date: 2018-06-08
Variant appearance in text: HR: Arg775His
PubMed Link:
29937999
Variant Present in the following documents:
Main text
View BVdb publication page