RET c.2331C>A ;(p.N777K)

Variant ID: 10-43613867-C-A

NM_020975.4(RET):c.2331C>A;(p.N777K)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Germline Predisposition to Pediatric Cancer, from Next Generation Sequencing to Medical Care.

Cancers
Gargallo, Pablo P; Oltra, Silvestre S; Yáñez, Yania Y; Juan-Ribelles, Antonio A; Calabria, Inés I; Segura, Vanessa V; Lázaro, Marián M; Balaguer, Julia J; Tormo, Teresa T; Dolz, Sandra S; Fernández, José María JM; Fuentes, Carolina C; Torres, Bárbara B; Andrés, Mara M; Tasso, María M; Castel, Victoria V; Font de Mora, Jaime J; Cañete, Adela A
Publication Date: 2021-10-24

Variant appearance in text: RET: 2331C>A; N777K
PubMed Link: 34771502
Variant Present in the following documents:
  • Main text
  • cancers-13-05339.pdf
View BVdb publication page



Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: RET: N777K
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page