MTRR c.*662T>G

Variant ID: 5-7900833-T-G

NM_002454.2(MTRR):c.*662T>G

This variant was identified in 15 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs8659
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs8659
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



MTRR rs1532268 polymorphism and gastric cancer risk: evidence from a meta-analysis.

The Journal Of International Medical Research
Zhong, Guping G; Luo, Xiaojin X; Li, Ji J; Liao, Yuanhang Y; Gui, Guan G; Sheng, Jianwen J
Publication Date: 2022-05

Variant appearance in text: rs8659
PubMed Link: 35579185
Variant Present in the following documents:
  • Main text
  • 10.1177_03000605221097486.pdf
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs8659
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs8659
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs8659
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs8659
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Genetic Variant in ACVR2B Is Associated with Lean Mass.

Medicine And Science In Sports And Exercise
Klimentidis, Yann C YC; Bea, Jennifer W JW; Thompson, Patricia P; Klimecki, Walter T WT; Hu, Chengcheng C; Wu, Guanglin G; Nicholas, J Skye JS; Ryckman, Kelli K KK; Chen, Zhao Z
Publication Date: 2016-07

Variant appearance in text: rs8659
PubMed Link: 26848890
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs8659
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.

Cephalalgia : An International Journal Of Headache
Roecklein, Kathryn A KA; Scher, Ann I AI; Smith, Albert A; Harris, Tamara T; Eiriksdottir, Gudny G; Garcia, Melissa M; Gudnason, Villi V; Launer, Lenore J LJ
Publication Date: 2013-05

Variant appearance in text: rs8659
PubMed Link: 23430981
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variant of AMD1 is associated with obesity in urban Indian children.

Plos One
Tabassum, Rubina R; Jaiswal, Alok A; Chauhan, Ganesh G; Dwivedi, Om Prakash OP; Ghosh, Saurabh S; Marwaha, Raman K RK; Tandon, Nikhil N; Bharadwaj, Dwaipayan D
Publication Date: 2012

Variant appearance in text: rs8659
PubMed Link: 22496743
Variant Present in the following documents:
View BVdb publication page



Genes and abdominal aortic aneurysm.

Annals Of Vascular Surgery
Hinterseher, Irene I; Tromp, Gerard G; Kuivaniemi, Helena H
Publication Date: 2011-04

Variant appearance in text: rs8659
PubMed Link: 21146954
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Genetic Epidemiology
Locke, Adam E AE; Dooley, Kenneth J KJ; Tinker, Stuart W SW; Cheong, Soo Yeon SY; Feingold, Eleanor E; Allen, Emily G EG; Freeman, Sallie B SB; Torfs, Claudine P CP; Cua, Clifford L CL; Epstein, Michael P MP; Wu, Michael C MC; Lin, Xihong X; Capone, George G; Sherman, Stephanie L SL; Bean, Lora J H LJ
Publication Date: 2010-09

Variant appearance in text: rs8659
PubMed Link: 20718043
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.

Journal Of Cancer Epidemiology
Van Dyke, Alison L AL; Cote, Michele L ML; Wenzlaff, Angela S AS; Abrams, Judith J; Land, Susan S; Iyer, Priyanka P; Schwartz, Ann G AG
Publication Date: 2009

Variant appearance in text: rs8659
PubMed Link: 20445798
Variant Present in the following documents:
  • Main text
View BVdb publication page



Blood leukocyte DNA hypomethylation and gastric cancer risk in a high-risk Polish population.

International Journal Of Cancer
Hou, Lifang L; Wang, Hao H; Sartori, Samantha S; Gawron, Andrew A; Lissowska, Jolanta J; Bollati, Valentina V; Tarantini, Letizia L; Zhang, Fang Fang FF; Zatonski, Witold W; Chow, Wong-Ho WH; Baccarelli, Andrea A
Publication Date: 2010-10-15

Variant appearance in text: rs8659
PubMed Link: 20099281
Variant Present in the following documents:
  • Main text
View BVdb publication page