Bibliome.ai browser hg19
Search
About
Stats
FAQ
MED23 c.2998C>G ;(p.R1000G)
Variant ID: 6-131915473-G-C
NM_004830.3(
MED23
):c.2998C>G;(p.R1000G)
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:
The genomic and epigenomic evolutionary history of papillary renal cell carcinomas.
Nature Communications
Zhu, Bin B; Poeta, Maria Luana ML; Costantini, Manuela M; Zhang, Tongwu T; Shi, Jianxin J; Sentinelli, Steno S; Zhao, Wei W; Pompeo, Vincenzo V; Cardelli, Maurizio M; Alexandrov, Boian S BS; Otlu, Burcak B; Hua, Xing X; Jones, Kristine K; Brodie, Seth S; Dabrowska, Malgorzata Ewa ME; Toro, Jorge R JR; Yeager, Meredith M; Wang, Mingyi M; Hicks, Belynda B; Alexandrov, Ludmil B LB; Brown, Kevin M KM; Wedge, David C DC; Chanock, Stephen S; Fazio, Vito Michele VM; Gallucci, Michele M; Landi, Maria Teresa MT
Publication Date: 2020-06-18
Variant appearance in text: MED23: R1000G
PubMed Link:
32555180
Variant Present in the following documents:
41467_2020_16546_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page