RET c.2897C>T ;(p.T966I)

Variant ID: 10-43619214-C-T

NM_020975.4(RET):c.2897C>T;(p.T966I)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Mutation Profile of Aggressive Pheochromocytoma and Paraganglioma with Comparison of TCGA Data.

Cancers
Choi, Yun Mi YM; Lim, Jinyeong J; Jeon, Min Ji MJ; Lee, Yu-Mi YM; Sung, Tae-Yon TY; Hong, Eun-Gyoung EG; Lee, Ji-Young JY; Jang, Se Jin SJ; Kim, Won Gu WG; Song, Dong Eun DE; Chun, Sung-Min SM
Publication Date: 2021-05-14

Variant appearance in text: RET: 2897C>T; Thr966Ile
PubMed Link: 34069252
Variant Present in the following documents:
  • Main text
  • cancers-13-02389.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: T966I
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Findings of a 1303 Korean whole-exome sequencing study.

Experimental & Molecular Medicine
Kwak, Soo Heon SH; Chae, Jeesoo J; Choi, Seongmin S; Kim, Min Jung MJ; Choi, Murim M; Chae, Jong-Hee JH; Cho, Eun-Hae EH; Hwang, Tai Ju TJ; Jang, Se Song SS; Kim, Jong-Il JI; Park, Kyong Soo KS; Bang, Yung-Jue YJ
Publication Date: 2017-07-14

Variant appearance in text: RET: T966I; rs760765930
PubMed Link: 28706299
Variant Present in the following documents:
  • emm2017142x4.xls, sheet 1
View BVdb publication page