MTHFR c.870C>T ;(p.N290=)

Variant ID: 1-11855316-G-A

NM_005957.4(MTHFR):c.870C>T;(p.N290=)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Saudi Journal Of Biological Sciences
Aboul-Soud, Mourad A M MAM; Alzahrani, Alhussain J AJ; Mahmoud, Amer A
Publication Date: 2021-01

Variant appearance in text: rs141769179
PubMed Link: 33424349
Variant Present in the following documents:
  • mmc1.xlsx, sheet 1
View BVdb publication page



Targeted next generation sequencing as a tool for precision medicine.

Bmc Medical Genomics
Gulilat, Markus M; Lamb, Tyler T; Teft, Wendy A WA; Wang, Jian J; Dron, Jacqueline S JS; Robinson, John F JF; Tirona, Rommel G RG; Hegele, Robert A RA; Kim, Richard B RB; Schwarz, Ute I UI
Publication Date: 2019-06-03

Variant appearance in text: rs141769179
PubMed Link: 31159795
Variant Present in the following documents:
  • 12920_2019_527_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page



The genetic component of preeclampsia: A whole-exome sequencing study.

Plos One
Hansen, Anette Tarp AT; Bernth Jensen, Jens Magnus JM; Hvas, Anne-Mette AM; Christiansen, Mette M
Publication Date: 2018

Variant appearance in text: MTHFR: 870C>T; N290N
PubMed Link: 29758065
Variant Present in the following documents:
  • Main text
  • pone.0197217.pdf
View BVdb publication page