MUTYH c.231C>T ;(p.D77=)

Variant ID: 1-45799118-G-A

NM_001048174.1(MUTYH):c.231C>T;(p.D77=)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Clinical relevance of pathogenic germline variants in mismatch repair genes in Chinese breast cancer patients.

Npj Breast Cancer
Hu, Li L; Sun, Jie J; Li, Zhongwu Z; Qu, Ziwei Z; Liu, Yan Y; Wan, Qiting Q; Liu, Jiaming J; Ding, Xinyun X; Zang, Fan F; Zhang, Juan J; Yao, Lu L; Xu, Ye Y; Wang, Yin Y; Xie, Yuntao Y
Publication Date: 2022-04-21

Variant appearance in text: MYH: 231C>T
PubMed Link: 35449176
Variant Present in the following documents:
  • 41523_2022_417_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer.

World Journal Of Gastrointestinal Oncology
Tezcan, Gulcin G; Tunca, Berrin B; Ak, Secil S; Cecener, Gulsah G; Egeli, Unal U
Publication Date: 2016-01-15

Variant appearance in text: MUTYH: 231C>T
PubMed Link: 26798439
Variant Present in the following documents:
  • Main text
View BVdb publication page