HERC2 c.5656G>C ;(p.G1886R)

Variant ID: 15-28465787-C-G

NM_004667.5(HERC2):c.5656G>C;(p.G1886R)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Publication Date: 2019-03-20

Variant appearance in text: HERC2: G1886R
PubMed Link: 30894629
Variant Present in the following documents:
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13
View BVdb publication page



The spectrum of somatic mutations in high-risk acute myeloid leukaemia with -7/del(7q).

British Journal Of Haematology
McNerney, Megan E ME; Brown, Christopher D CD; Peterson, April L AL; Banerjee, Mekhala M; Larson, Richard A RA; Anastasi, John J; Le Beau, Michelle M MM; White, Kevin P KP
Publication Date: 2014-08

Variant appearance in text: HERC2: G1886R
PubMed Link: 24931631
Variant Present in the following documents:
  • Main text
View BVdb publication page