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HR c.773G>A ;(p.G258D)
Variant ID: 8-21985182-C-T
NM_005144.4(
HR
):c.773G>A;(p.G258D)
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:
Single-cell transcriptomic analysis suggests two molecularly subtypes of intrahepatic cholangiocarcinoma.
Nature Communications
Song, Guohe G; Shi, Yang Y; Meng, Lu L; Ma, Jiaqiang J; Huang, Siyuan S; Zhang, Juan J; Wu, Yingcheng Y; Li, Jiaxin J; Lin, Youpei Y; Yang, Shuaixi S; Rao, Dongning D; Cheng, Yifei Y; Lin, Jian J; Ji, Shuyi S; Liu, Yuming Y; Jiang, Shan S; Wang, Xiaoliang X; Zhang, Shu S; Ke, Aiwu A; Wang, Xiaoying X; Cao, Ya Y; Ji, Yuan Y; Zhou, Jian J; Fan, Jia J; Zhang, Xiaoming X; Xi, Ruibin R; Gao, Qiang Q
Publication Date: 2022-03-28
Variant appearance in text: HR: 773G>A; G258D
PubMed Link:
35347134
Variant Present in the following documents:
41467_2022_29164_MOESM13_ESM.xlsx, sheet 9
View BVdb publication page
Interplay between Fanconi anemia and homologous recombination pathways in genome integrity.
The Embo Journal
Michl, Johanna J; Zimmer, Jutta J; Tarsounas, Madalena M
Publication Date: 2016-05-02
Variant appearance in text: HR: 773G>A
PubMed Link:
27037238
Variant Present in the following documents:
Main text
EMBJ-35-909.pdf
View BVdb publication page