GALNT2 c.*1116C>T

Variant ID: 1-230416320-C-T

NM_004481.3(GALNT2):c.*1116C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


CETP genetic variant rs1800777 (allele A) is associated with abnormally low HDL-C levels and increased risk of AKI during sepsis.

Scientific Reports
Genga, Kelly Roveran KR; Trinder, Mark M; Kong, HyeJin Julia HJ; Li, Xuan X; Leung, Alex K K AKK; Shimada, Tadanaga T; Walley, Keith R KR; Russell, James A JA; Francis, Gordon A GA; Brunham, Liam R LR; Boyd, John H JH
Publication Date: 2018-11-13

Variant appearance in text: rs3213497
PubMed Link: 30425299
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_35261.pdf
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs3213497
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page