CD5 c.949C>T ;(p.R317W)

Variant ID: 11-60889226-C-T

NM_014207.3(CD5):c.949C>T;(p.R317W)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Effect of rare coding variants in the CFI gene on Factor I expression levels.

Human Molecular Genetics
de Jong, Sarah S; Volokhina, Elena B EB; de Breuk, Anita A; Nilsson, Sara C SC; de Jong, Eiko K EK; van der Kar, Nicole C A J NCAJ; Bakker, Bjorn B; Hoyng, Carel B CB; van den Heuvel, Lambert P LP; Blom, Anna M AM; den Hollander, Anneke I AI
Publication Date: 2020-08-11

Variant appearance in text: CD5: Arg317Trp
PubMed Link: 32510551
Variant Present in the following documents:
  • supp_table_1_ddaa114.xlsx, sheet 1
View BVdb publication page



Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers.

Cell Reports
Cheng, Hui H; Yang, Xinping X; Si, Han H; Saleh, Anthony D AD; Xiao, Wenming W; Coupar, Jamie J; Gollin, Susanne M SM; Ferris, Robert L RL; Issaeva, Natalia N; Yarbrough, Wendell G WG; Prince, Mark E ME; Carey, Thomas E TE; Van Waes, Carter C; Chen, Zhong Z
Publication Date: 2018-10-30

Variant appearance in text: CD5: R317W; rs147649434
PubMed Link: 30380422
Variant Present in the following documents:
  • NIHMS1511993-supplement-6.xlsx, sheet 1
View BVdb publication page



Atypical hemolytic uremic syndrome.

Seminars In Nephrology
Kavanagh, David D; Goodship, Tim H TH; Richards, Anna A
Publication Date: 2013-11

Variant appearance in text: CD5: R317W
PubMed Link: 24161037
Variant Present in the following documents:
  • Main text
View BVdb publication page