MSH6 c.4051C>G ;(p.H1351D)

Variant ID: 2-48033967-C-G

NM_000179.2(MSH6):c.4051C>G;(p.H1351D)

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: MSH6: 4051C>G; H1351D
PubMed Link: 35449176
Variant Present in the following documents:
  • 41523_2022_417_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China.

Cancer Communications (London, England)
Chao, Xiaopei X; Li, Lei L; Wu, Ming M; Ma, Shuiqing S; Tan, Xianjie X; Zhong, Sen S; Bi, Yalan Y; Lang, Jinghe J
Publication Date: 2019-07-15

Variant appearance in text: MSH6: His1351Asp
PubMed Link: 31307542
Variant Present in the following documents:
  • Main text
  • 40880_2019_Article_388.pdf
View BVdb publication page