MLH1 c.1731+18del

Variant ID: 3-37083836-CT-C

NM_000249.3(MLH1):c.1731+18del

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prevalence and spectrum of DNA mismatch repair gene variation in the general Chinese population.

Journal Of Medical Genetics
Zhang, Li L; Qin, Zixin Z; Huang, Teng T; Tam, Benjamin B; Ruan, Yongsen Y; Guo, Maoni M; Wu, Xiaobing X; Li, Jiaheng J; Zhao, Bojin B; Chian, Jia Sheng JS; Wang, Xiaoyu X; Wang, Lei L; Wang, San Ming SM
Publication Date: 2022-07

Variant appearance in text: MLH1: 1731+15delT
PubMed Link: 34172528
Variant Present in the following documents:
  • jmedgenet-2021-107886supp006.xlsx, sheet 1
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Advances in the study of Lynch syndrome in China.

World Journal Of Gastroenterology
Lu, Jun-Yu JY; Sheng, Jian-Qiu JQ
Publication Date: 2015-06-14

Variant appearance in text: MLH1: 1731+15delT
PubMed Link: 26078562
Variant Present in the following documents:
  • Main text
View BVdb publication page