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ALK c.1204G>A ;(p.V402M)
Variant ID: 2-29606676-C-T
NM_004304.4(
ALK
):c.1204G>A;(p.V402M)
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:
A molecular approach integrating genomic and DNA methylation profiling for tissue of origin identification in lung-specific cancer of unknown primary.
Journal Of Translational Medicine
Chen, Kaiyan K; Zhang, Fanrong F; Yu, Xiaoqing X; Huang, Zhiyu Z; Gong, Lei L; Xu, Yanjun Y; Li, Hui H; Yu, Sizhe S; Fan, Yun Y
Publication Date: 2022-04-05
Variant appearance in text: ALK: V402M
PubMed Link:
35382836
Variant Present in the following documents:
12967_2022_Article_3362.pdf
View BVdb publication page
Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
Plos Genetics
Yehia, Lamis L; Ni, Ying Y; Sesock, Kaitlin K; Niazi, Farshad F; Fletcher, Benjamin B; Chen, Hannah Jin Lian HJL; LaFramboise, Thomas T; Eng, Charis C
Publication Date: 2018-04
Variant appearance in text: ALK: V402M
PubMed Link:
29684080
Variant Present in the following documents:
pgen.1007352.s009.xlsx, sheet 1
View BVdb publication page