F5 c.2707G>A ;(p.G903R)

Variant ID: 1-169511621-C-T

NM_000130.4(F5):c.2707G>A;(p.G903R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Actionable, pathogenic incidental findings in 1,000 participants' exomes.

American Journal Of Human Genetics
Dorschner, Michael O MO; Amendola, Laura M LM; Turner, Emily H EH; Robertson, Peggy D PD; Shirts, Brian H BH; Gallego, Carlos J CJ; Bennett, Robin L RL; Jones, Kelly L KL; Tokita, Mari J MJ; Bennett, James T JT; Kim, Jerry H JH; Rosenthal, Elisabeth A EA; Kim, Daniel S DS; , ; Tabor, Holly K HK; Bamshad, Michael J MJ; Motulsky, Arno G AG; Scott, C Ronald CR; Pritchard, Colin C CC; Walsh, Tom T; Burke, Wylie W; Raskind, Wendy H WH; Byers, Peter P; Hisama, Fuki M FM; Nickerson, Deborah A DA; Jarvik, Gail P GP
Publication Date: 2013-10-03

Variant appearance in text: F5: 2707G>A
PubMed Link: 24055113
Variant Present in the following documents:
  • Main text
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