TLR4 c.774G>T ;(p.L258F)

Variant ID: 9-120475180-G-T

NM_138554.4(TLR4):c.774G>T;(p.L258F)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: TLR4: L258F
PubMed Link: 35449176
Variant Present in the following documents:
  • 41523_2022_417_MOESM1_ESM.pdf
  • 41523_2022_417_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page