TCN2 c.1196G>C ;(p.R399P)

Variant ID: 22-31019044-G-C

NM_000355.3(TCN2):c.1196G>C;(p.R399P)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Pathway analysis of genetic variants in folate-mediated one-carbon metabolism-related genes and survival in a prospectively followed cohort of colorectal cancer patients.

Cancer Medicine
Ose, Jennifer J; Botma, Akke A; Balavarca, Yesilda Y; Buck, Katharina K; Scherer, Dominique D; Habermann, Nina N; Beyerle, Jolantha J; Pfütze, Katrin K; Seibold, Petra P; Kap, Elisabeth J EJ; Benner, Axel A; Jansen, Lina L; Butterbach, Katja K; Hoffmeister, Michael M; Brenner, Hermann H; Ulrich, Alexis A; Schneider, Martin M; Chang-Claude, Jenny J; Burwinkel, Barbara B; Ulrich, Cornelia M CM
Publication Date: 2018-07

Variant appearance in text: rs4820889
PubMed Link: 29845757
Variant Present in the following documents:
  • Main text
  • CAM4-7-2797.pdf
View BVdb publication page



Pathway analysis of genetic variants in folate-mediated one-carbon metabolism-related genes and survival in a prospectively followed cohort of colorectal cancer patients.

Cancer Medicine
Ose, Jennifer J; Botma, Akke A; Balavarca, Yesilda Y; Buck, Katharina K; Scherer, Dominique D; Habermann, Nina N; Beyerle, Jolantha J; Pfütze, Katrin K; Seibold, Petra P; Kap, Elisabeth J EJ; Benner, Axel A; Jansen, Lina L; Butterbach, Katja K; Hoffmeister, Michael M; Brenner, Hermann H; Ulrich, Alexis A; Schneider, Martin M; Chang-Claude, Jenny J; Burwinkel, Barbara B; Ulrich, Cornelia M CM
Publication Date: 2018-05-29

Variant appearance in text: rs4820889
PubMed Link: 29845757
Variant Present in the following documents:
  • Main text
  • CAM4-7-2797.pdf
View BVdb publication page



XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One
Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F
Publication Date: 2015

Variant appearance in text: rs4820889
PubMed Link: 25905921
Variant Present in the following documents:
  • pone.0123569.s008.xls, sheet 5
  • pone.0123569.s008.xls, sheet 10
View BVdb publication page



Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports
Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R
Publication Date: 2015-03-16

Variant appearance in text: rs4820889
PubMed Link: 25773295
Variant Present in the following documents:
  • srep09124-s3.xls, sheet 1
View BVdb publication page



Neural tube defects, folic acid and methylation.

International Journal Of Environmental Research And Public Health
Imbard, Apolline A; Benoist, Jean-François JF; Blom, Henk J HJ
Publication Date: 2013-09-17

Variant appearance in text: rs4820889
PubMed Link: 24048206
Variant Present in the following documents:
  • Main text
  • ijerph-10-04352.pdf
View BVdb publication page



Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.

Neurology
Hsu, F-C FC; Sides, E G EG; Mychaleckyj, J C JC; Worrall, B B BB; Elias, G A GA; Liu, Y Y; Chen, W-M WM; Coull, B M BM; Toole, J F JF; Rich, S S SS; Furie, K L KL; Sale, M M MM
Publication Date: 2011-10-18

Variant appearance in text: rs4820889
PubMed Link: 21975197
Variant Present in the following documents:
  • Main text
View BVdb publication page