F2 c.877G>A ;(p.E293K)

Variant ID: 11-46748050-G-A

NM_000506.3(F2):c.877G>A;(p.E293K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation discovery in mice by whole exome sequencing.

Genome Biology
Fairfield, Heather H; Gilbert, Griffith J GJ; Barter, Mary M; Corrigan, Rebecca R RR; Curtain, Michelle M; Ding, Yueming Y; D'Ascenzo, Mark M; Gerhardt, Daniel J DJ; He, Chao C; Huang, Wenhui W; Richmond, Todd T; Rowe, Lucy L; Probst, Frank J FJ; Bergstrom, David E DE; Murray, Stephen A SA; Bult, Carol C; Richardson, Joel J; Kile, Benjamin T BT; Gut, Ivo I; Hager, Jorg J; Sigurdsson, Snaevar S; Mauceli, Evan E; Di Palma, Federica F; Lindblad-Toh, Kerstin K; Cunningham, Michael L ML; Cox, Timothy C TC; Justice, Monica J MJ; Spector, Mona S MS; Lowe, Scott W SW; Albert, Thomas T; Donahue, Leah Rae LR; Jeddeloh, Jeffrey J; Shendure, Jay J; Reinholdt, Laura G LG
Publication Date: 2011-09-14

Variant appearance in text: F2: E293K
PubMed Link: 21917142
Variant Present in the following documents:
  • Main text
  • gb-2011-12-9-r86.pdf
View BVdb publication page