MTHFR c.681G>A ;(p.T227=)

Variant ID: 1-11856362-C-T

NM_005957.4(MTHFR):c.681G>A;(p.T227=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Integrative proteogenomic characterization of early esophageal cancer.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Zhang, Qiao Q; Liu, Hui H; Xu, Fujiang F; Guo, Chunmei C; Qin, Zhaoyu Z; Wang, Haixing H; Feng, Jinwen J; Liu, Yang Y; Chen, Weijie W; Zhang, Xue X; Bai, Lin L; Tian, Sha S; Tan, Subei S; Xu, Chen C; Song, Qi Q; Liu, Yalan Y; Zhong, Yunshi Y; Chen, Tianyin T; Zhou, Pinghong P; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-25

Variant appearance in text: MTHFR: T227T; rs774825800
PubMed Link: 36966136
Variant Present in the following documents:
  • 41467_2023_37440_MOESM4_ESM.xlsx, sheet 2
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MAT1A variants are associated with hypertension, stroke, and markers of DNA damage and are modulated by plasma vitamin B-6 and folate.

The American Journal Of Clinical Nutrition
Lai, Chao-Qiang CQ; Parnell, Laurence D LD; Troen, Aron M AM; Shen, Jian J; Caouette, Heather H; Warodomwichit, Daruneewan D; Lee, Yu-Chi YC; Crott, Jimmy W JW; Qiu, Wei Qiao WQ; Rosenberg, Irwin H IH; Tucker, Katherine L KL; Ordovás, José M JM
Publication Date: 2010-05

Variant appearance in text:
PubMed Link: 20335551
Variant Present in the following documents:
  • Main text
View BVdb publication page