SREBF2 c.2738+465C>G

Variant ID: 22-42295250-C-G

NM_004599.3(SREBF2):c.2738+465C>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Somatic Mutation Profiling of Papillary Thyroid Carcinomas by Whole-exome Sequencing and Its Relationship with Clinical Characteristics.

International Journal Of Medical Sciences
Qi, Tingyue T; Rong, Xin X; Feng, Qingling Q; Sun, Hongguang H; Cao, Haiyan H; Yang, Yan Y; Feng, Hao H; Zhu, Linhai L; Wang, Lei L; Du, Qiu Q
Publication Date: 2021

Variant appearance in text: rs713881
PubMed Link: 34104084
Variant Present in the following documents:
  • ijmsv18p2532s2.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs713881
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22.

Human Genomics
González-Neira, Anna A; Calafell, Francesc F; Navarro, Arcadi A; Lao, Oscar O; Cann, Howard H; Comas, David D; Bertranpetit, Jaume J
Publication Date: 2004-11

Variant appearance in text: rs713881
PubMed Link: 15606995
Variant Present in the following documents:
  • Main text
  • 1479-7364-1-6-399.pdf
View BVdb publication page