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LRP1B c.5006A>C ;(p.E1669A)
Variant ID: 2-141598595-T-G
NM_018557.2(
LRP1B
):c.5006A>C;(p.E1669A)
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:
Integrative analysis reveals clinically relevant molecular fingerprints in pancreatic cancer.
Molecular Therapy. Nucleic Acids
Song, Libin L; Qi, Simin S; Hu, Wei W; Fang, Zhixiao Z; Yu, Dehua D; Liu, Teng T; Wu, Jingni J; Wu, Yangjun Y; Wu, Aiwei A; Feng, Lanyun L; Xie, Jing J; Zhang, Bo B; He, Wenguang W; Ning, Zhouyu Z; Liu, Luming L; Qin, Jiang-Jiang JJ; Li, Shengli S
Publication Date: 2021-12-03
Variant appearance in text: LRP1B: 5006A>C; E1669A
PubMed Link:
34513290
Variant Present in the following documents:
mmc3.xlsx, sheet 1
View BVdb publication page
The Gain-of-Function p53 R248W Mutant Promotes Migration by STAT3 Deregulation in Human Pancreatic Cancer Cells.
Frontiers In Oncology
Klemke, Luisa L; Fehlau, Clara F CF; Winkler, Nadine N; Toboll, Felicia F; Singh, Shiv K SK; Moll, Ute M UM; Schulz-Heddergott, Ramona R
Publication Date: 2021
Variant appearance in text: LRP1B: 5006A>C; Glu1669Ala
PubMed Link:
34178628
Variant Present in the following documents:
DataSheet_1.pdf
View BVdb publication page