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ALK c.3476A>T ;(p.Q1159L)
Variant ID: 2-29445249-T-A
NM_004304.4(
ALK
):c.3476A>T;(p.Q1159L)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study.
Frontiers In Genetics
Huang, Yanlin Y; Liu, Chang C; Ding, Hongke H; Wang, Yunan Y; Yu, Lihua L; Guo, Fangfang F; Li, Fake F; Shi, Xiaomei X; Zhang, Yan Y; Yin, Aihua A
Publication Date: 2023
Variant appearance in text: ALK: 3476A>T; Gln1159Leu
PubMed Link:
36923788
Variant Present in the following documents:
Table3.xlsx, sheet 1
View BVdb publication page
Profiling Oncogenic Germline Mutations in Unselected Chinese Lung Cancer Patients.
Frontiers In Oncology
Yang, Jie J; Li, Hefei H; Li, Ben B; Li, Wei W; Guo, Qiang Q; Hu, Ling L; Song, Zizheng Z; Zhou, Bin B
Publication Date: 2021
Variant appearance in text: ALK: Q1159L
PubMed Link:
33898318
Variant Present in the following documents:
Main text
View BVdb publication page
Identification of pathogenic missense mutations using protein stability predictors.
Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21
Variant appearance in text: ALK: Q1159L
PubMed Link:
32958805
Variant Present in the following documents:
41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page