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LRP1B c.4934C>G ;(p.S1645*)
Variant ID: 2-141607676-G-C
NM_018557.2(
LRP1B
):c.4934C>G;(p.S1645*)
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:
Identification of the TP53 p.R337H Variant in Tumor Genomic Profiling Should Prompt Consideration of Germline Testing for Li-Fraumeni Syndrome.
Jco Global Oncology
Sandoval, Renata Lazari RL; Masotti, Cibele C; de Macedo, Mariana Petaccia MP; Ribeiro, MaurĂcio Fernando Silva Almeida MFSA; Leite, Ana Carolina Rathsam ACR; Meireles, Sibele Inacio SI; Bovolin, Rodrigo Medeiros RM; Santini, Fernando Costa FC; Munhoz, Rodrigo Ramella RR; Jardim, Denis Leonardo Fontes DLF; Katz, Artur A; Camargo, Anamaria Aranha AA; Fernandes, Gustavo Dos Santos GDS; Achatz, Maria Isabel MI
Publication Date: 2021-07
Variant appearance in text: LRP1B: S1645*
PubMed Link:
34270331
Variant Present in the following documents:
go-7-go.21.00097.pdf
View BVdb publication page