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KRAS c.276T>C ;(p.D92=)
Variant ID: 12-25380182-A-G
NM_004985.3(
KRAS
):c.276T>C;(p.D92=)
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:
Identifying the Steps Required to Effectively Implement Next-Generation Sequencing in Oncology at a National Level in Europe.
Journal Of Personalized Medicine
Horgan, Denis D; Curigliano, Giuseppe G; Rieß, Olaf O; Hofman, Paul P; Büttner, Reinhard R; Conte, Pierfranco P; Cufer, Tanja T; Gallagher, William M WM; Georges, Nadia N; Kerr, Keith K; Penault-Llorca, Frédérique F; Mastris, Ken K; Pinto, Carla C; Van Meerbeeck, Jan J; Munzone, Elisabetta E; Thomas, Marlene M; Ujupan, Sonia S; Vainer, Gilad W GW; Velthaus, Janna-Lisa JL; André, Fabrice F
Publication Date: 2022-01-08
Variant appearance in text: KRAS: D92D
PubMed Link:
35055387
Variant Present in the following documents:
Main text
View BVdb publication page