HR c.335G>C ;(p.G112A)

Variant ID: 8-21986349-C-G

NM_005144.4(HR):c.335G>C;(p.G112A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Allelic Complexity in Long QT Syndrome: A Family-Case Study.

International Journal Of Molecular Sciences
Zullo, Alberto A; Frisso, Giulia G; Detta, Nicola N; Sarubbi, Berardo B; Romeo, Emanuele E; Cordella, Angela A; Vanoye, Carlos G CG; CalabrĂ², Raffaele R; George, Alfred L AL; Salvatore, Francesco F
Publication Date: 2017-07-27

Variant appearance in text: HR: G112A
PubMed Link: 28749435
Variant Present in the following documents:
  • Main text
  • ijms-18-01633.pdf
View BVdb publication page



Role of sequence and structure of the Hendra fusion protein fusion peptide in membrane fusion.

The Journal Of Biological Chemistry
Smith, Everett Clinton EC; Gregory, Sonia M SM; Tamm, Lukas K LK; Creamer, Trevor P TP; Dutch, Rebecca Ellis RE
Publication Date: 2012-08-24

Variant appearance in text: HR: G112A
PubMed Link: 22761418
Variant Present in the following documents:
  • Main text
View BVdb publication page