Bibliome.ai browser hg19
Search
About
Stats
FAQ
PARD3 c.2573C>G ;(p.T858S)
Variant ID: 10-34625159-G-C
NM_001184785.1(
PARD3
):c.2573C>G;(p.T858S)
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:
Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels.
Plos One
Toyama, Miho M; Takasaki, Yuto Y; Branko, Aleksic A; Kimura, Hiroki H; Kato, Hidekazu H; Nawa, Yoshihiro Y; Kushima, Itaru I; Ishizuka, Kanako K; Shimamura, Teppei T; Ogi, Tomoo T; Ozaki, Norio N
Publication Date: 2022
Variant appearance in text: PARD3: T858S
PubMed Link:
35536790
Variant Present in the following documents:
pone.0268321.s003.xlsx, sheet 1
View BVdb publication page
Genomic characterization of a large panel of patient-derived hepatocellular carcinoma xenograft tumor models for preclinical development.
Oncotarget
Gu, Qingyang Q; Zhang, Bin B; Sun, Hongye H; Xu, Qiang Q; Tan, Yexiong Y; Wang, Guan G; Luo, Qin Q; Xu, Weiguo W; Yang, Shuqun S; Li, Jian J; Fu, Jing J; Chen, Lei L; Yuan, Shengxian S; Liang, Guibai G; Ji, Qunsheng Q; Chen, Shu-Hui SH; Chan, Chi-Chung CC; Zhou, Weiping W; Xu, Xiaowei X; Wang, Hongyang H; Fang, Douglas D DD
Publication Date: 2015-08-21
Variant appearance in text: PARD3: T858S
PubMed Link:
26062443
Variant Present in the following documents:
oncotarget-06-20160-s004.xlsx, sheet 1
View BVdb publication page