NTRK2 c.1396+38212G>A

Variant ID: 9-87405212-G-A

NM_006180.3(NTRK2):c.1396+38212G>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics
Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y
Publication Date: 2022

Variant appearance in text: NTRK2: 1396+38212G>A
PubMed Link: 35899134
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications
Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C
Publication Date: 2019-08-30

Variant appearance in text: rs1662695
PubMed Link: 31470906
Variant Present in the following documents:
  • 40478_2019_793_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach.

Plos One
Hennings, Johannes M JM; Kohli, Martin A MA; Czamara, Darina D; Giese, Maria M; Eckert, Anne A; Wolf, Christiane C; Heck, Angela A; Domschke, Katharina K; Arolt, Volker V; Baune, Bernhard T BT; Horstmann, Sonja S; Brückl, Tanja T; Klengel, Torsten T; Menke, Andreas A; Müller-Myhsok, Bertram B; Ising, Marcus M; Uhr, Manfred M; Lucae, Susanne S
Publication Date: 2013

Variant appearance in text: rs1662695
PubMed Link: 23750220
Variant Present in the following documents:
  • Main text
  • pone.0064947.pdf
View BVdb publication page



Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.

American Journal Of Medical Genetics. Part A
Shi, Min M; Murray, Jeffrey C JC; Marazita, Mary L ML; Munger, Ronald G RG; Ruczinski, Ingo I; Hetmanski, Jacqueline B JB; Wu, Tao T; Murray, Tanda T; Redett, Richard J RJ; Wilcox, Allen J AJ; Lie, Rolv T RT; Jabs, Ethylin Wang EW; Wu-Chou, Yah Huei YH; Chen, Philip K PK; Wang, Hong H; Ye, Xiaoqian X; Yeow, Vincent V; Chong, Samuel S SS; Shi, Bing B; Christensen, Kaare K; Scott, Alan F AF; Patel, Poorav P; Cheah, Felicia F; Beaty, Terri H TH
Publication Date: 2012-04

Variant appearance in text: rs1662695
PubMed Link: 22419666
Variant Present in the following documents:
  • Main text
View BVdb publication page