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CUX1 c.743G>T ;(p.R248I)
Variant ID: 7-101813745-G-T
NM_181552.3(
CUX1
):c.743G>T;(p.R248I)
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:
Construction and validation of an immunoediting-based optimized neoantigen load (ioTNL) model to predict the response and prognosis of immune checkpoint therapy in various cancers.
Aging
Su, Xiaofan X; Jin, Haoxuan H; Wang, Jiaqian J; Lu, Huiping H; Gu, Tiantian T; Gao, Zhibo Z; Li, Manxiang M
Publication Date: 2022-05-25
Variant appearance in text: CUX1: 743G>T; R248L
PubMed Link:
35613927
Variant Present in the following documents:
aging-14-204101-s004.xlsx, sheet 1
View BVdb publication page
Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia.
Scientific Reports
Kim, Borahm B; Yun, Woobin W; Lee, Seung-Tae ST; Choi, Jong Rok JR; Yoo, Keon Hee KH; Koo, Hong Hoe HH; Jung, Chul Won CW; Kim, Sun Hee SH
Publication Date: 2020-08-31
Variant appearance in text: CUX1: 743G>T; Arg248Leu
PubMed Link:
32868804
Variant Present in the following documents:
41598_2020_71386_MOESM1_ESM.pdf
View BVdb publication page