KMT2C c.4035G>T ;(p.K1345N)

Variant ID: 7-151900076-C-A

NM_170606.2(KMT2C):c.4035G>T;(p.K1345N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical characteristics and genetic analysis of gene mutations in a Chinese pedigree with Peutz-Jeghers syndrome.

Clinical Case Reports
Qiu, Yudian Y; Xuan, Tao T; Yin, Mujun M; Gao, Zhidong Z; Guo, Peng P; Chen, Xi X; Ye, Yingjiang Y; Shen, Zhanlong Z
Publication Date: 2019-04

Variant appearance in text: MLL3: 4035G>T
PubMed Link: 30997075
Variant Present in the following documents:
  • Main text
  • CCR3-7-735.pdf
View BVdb publication page