EPN3 c.*999G>A

Variant ID: 17-48620517-G-A

NM_017957.2(EPN3):c.*999G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs4793661
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.

Molecular Psychiatry
Strom, S P SP; Stone, J L JL; Ten Bosch, J R JR; Merriman, B B; Cantor, R M RM; Geschwind, D H DH; Nelson, S F SF
Publication Date: 2010-10

Variant appearance in text: rs4793661
PubMed Link: 19455149
Variant Present in the following documents:
  • Main text
View BVdb publication page