RET c.2172G>C ;(p.L724F)

Variant ID: 10-43612067-G-C

NM_020975.4(RET):c.2172G>C;(p.L724F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of RUNX1T1 as a potential epigenetic modifier in small-cell lung cancer.

Molecular Oncology
He, Tian T; Wildey, Gary G; McColl, Karen K; Savadelis, Alyssa A; Spainhower, Kyle K; McColl, Cassidy C; Kresak, Adam A; Tan, Aik Choon AC; Yang, Michael M; Abbas, Ata A; Dowlati, Afshin A
Publication Date: 2021-01

Variant appearance in text: RET: L724F
PubMed Link: 33084222
Variant Present in the following documents:
  • Main text
  • MOL2-15-195.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: L724F
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page