Bibliome.ai browser hg19
Search
About
Stats
FAQ
PPP1R3A c.2743C>T ;(p.P915S)
Variant ID: 7-113518404-G-A
NM_002711.3(
PPP1R3A
):c.2743C>T;(p.P915S)
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:
Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.
Bmc Medical Genomics
Ye, Lihua L; Wang, Li L; Peng, Kexin K; Fang, Ou O; Tian, Zhen Z; Li, Caihua C; Fu, Xiaopeng X; Chen, Qingdong Q; Chen, Jia J; Luan, Jing J; Zhang, Zhenghua Z; Zhang, Qiaoan Q
Publication Date: 2022-08-05
Variant appearance in text: PPP1R3A: 2743C>T; Pro915Ser
PubMed Link:
35932013
Variant Present in the following documents:
12920_2022_1324_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page
The landscape of driver mutations in cutaneous squamous cell carcinoma.
Npj Genomic Medicine
Chang, Darwin D; Shain, A Hunter AH
Publication Date: 2021-07-16
Variant appearance in text: PPP1R3A: P915S
PubMed Link:
34272401
Variant Present in the following documents:
41525_2021_226_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page