HPSE2 c.*1452C>T

Variant ID: 10-100217879-G-A

NM_021828.4(HPSE2):c.*1452C>T

This variant was identified in 1 publication

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: rs4917834
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page