RET c.844G>T ;(p.V282L)

Variant ID: 10-43600618-G-T

NM_020975.4(RET):c.844G>T;(p.V282L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients.

Nature Communications
Zhang, Yongliang Y; Yao, Yu Y; Xu, Yaping Y; Li, Lifeng L; Gong, Yan Y; Zhang, Kai K; Zhang, Meng M; Guan, Yanfang Y; Chang, Lianpeng L; Xia, Xuefeng X; Li, Lin L; Jia, Shuqin S; Zeng, Qiang Q
Publication Date: 2021-01-04

Variant appearance in text: RET: 844G>T; V282L
PubMed Link: 33397889
Variant Present in the following documents:
  • 41467_2020_20162_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.

Scientific Reports
Luzón-Toro, Berta B; Gui, Hongsheng H; Ruiz-Ferrer, Macarena M; Sze-Man Tang, Clara C; Fernández, Raquel M RM; Sham, Pak-Chung PC; Torroglosa, Ana A; Kwong-Hang Tam, Paul P; Espino-Paisán, Laura L; Cherny, Stacey S SS; Bleda, Marta M; Enguix-Riego, María Del Valle Mdel V; Dopazo, Joaquín J; Antiñolo, Guillermo G; García-Barceló, María-Mercé MM; Borrego, Salud S
Publication Date: 2015-11-12

Variant appearance in text: RET: Val282Leu
PubMed Link: 26559152
Variant Present in the following documents:
  • Main text
  • srep16473.pdf
View BVdb publication page