Bibliome.ai browser hg19
Search
About
Stats
FAQ
HR c.1838G>A ;(p.R613Q)
Variant ID: 8-21981239-C-T
NM_005144.4(
HR
):c.1838G>A;(p.R613Q)
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:
Somatic alterations and mutational burden are potential predictive factors for metachronous development of early gastric cancer.
Scientific Reports
Sakuta, Kazuhiro K; Sasaki, Yu Y; Abe, Yasuhiko Y; Sato, Hidenori H; Shoji, Masakuni M; Yaoita, Takao T; Yagi, Makoto M; Mizumoto, Naoko N; Onozato, Yusuke Y; Kon, Takashi T; Koseki, Ayumi A; Sato, Sonoko S; Murakami, Ryoko R; Miyano, Yuki Y; Ueno, Yoshiyuki Y
Publication Date: 2020-12-16
Variant appearance in text: HR: R613Q
PubMed Link:
33328548
Variant Present in the following documents:
41598_2020_79195_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page
Stabilization of the Reductase Domain in the Catalytically Self-Sufficient Cytochrome P450BM3 by Consensus-Guided Mutagenesis.
Chembiochem : A European Journal Of Chemical Biology
Saab-Rincón, Gloria G; Alwaseem, Hanan H; Guzmán-Luna, Valeria V; Olvera, Leticia L; Fasan, Rudi R
Publication Date: 2018-03-16
Variant appearance in text: HR: R613Q
PubMed Link:
29276819
Variant Present in the following documents:
Main text
View BVdb publication page