PC c.1160T>C ;(p.F387S)

Variant ID: 11-66633683-A-G

NM_001040716.1(PC):c.1160T>C;(p.F387S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.

Plos Genetics
Qi, Hongjian H; Yu, Lan L; Zhou, Xueya X; Wynn, Julia J; Zhao, Haoquan H; Guo, Yicheng Y; Zhu, Na N; Kitaygorodsky, Alexander A; Hernan, Rebecca R; Aspelund, Gudrun G; Lim, Foong-Yen FY; Crombleholme, Timothy T; Cusick, Robert R; Azarow, Kenneth K; Danko, Melissa E ME; Chung, Dai D; Warner, Brad W BW; Mychaliska, George B GB; Potoka, Douglas D; Wagner, Amy J AJ; ElFiky, Mahmoud M; Wilson, Jay M JM; Nickerson, Debbie D; Bamshad, Michael M; High, Frances A FA; Longoni, Mauro M; Donahoe, Patricia K PK; Chung, Wendy K WK; Shen, Yufeng Y
Publication Date: 2018-12

Variant appearance in text: PC: 1160T>C; F387S
PubMed Link: 30532227
Variant Present in the following documents:
  • Main text
  • pgen.1007822.pdf
View BVdb publication page