ALK c.667+63902A>C

Variant ID: 2-30078957-T-G

NM_004304.4(ALK):c.667+63902A>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs4581855
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs4581855
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

Human Genetics
Bostrom, Meredith A MA; Lu, Lingyi L; Chou, Jeff J; Hicks, Pamela J PJ; Xu, Jianzhao J; Langefeld, Carl D CD; Bowden, Donald W DW; Freedman, Barry I BI
Publication Date: 2010-08

Variant appearance in text: rs4581855
PubMed Link: 20532800
Variant Present in the following documents:
  • Main text
View BVdb publication page