F8 c.239T>C ;(p.I80T)

Variant ID: X-154227780-A-G

NM_000132.3(F8):c.239T>C;(p.I80T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome resequencing and bioinformatic analysis of SNP containing candidate genes in the autoimmune vitiligo Smyth line chicken model.

Bmc Genomics
Jang, Hyeon-Min HM; Erf, Gisela F GF; Rowland, Kaylee C KC; Kong, Byung-Whi BW
Publication Date: 2014-08-23

Variant appearance in text: F8: 239T>C
PubMed Link: 25151476
Variant Present in the following documents:
  • 12864_2013_6386_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Mutational and structural analysis of KIR3DL1 reveals a lineage-defining allotypic dimorphism that impacts both HLA and peptide sensitivity.

Journal Of Immunology (Baltimore, Md. : 1950)
O'Connor, Geraldine M GM; Vivian, Julian P JP; Widjaja, Jacqueline M JM; Bridgeman, John S JS; Gostick, Emma E; Lafont, Bernard A P BA; Anderson, Stephen K SK; Price, David A DA; Brooks, Andrew G AG; Rossjohn, Jamie J; McVicar, Daniel W DW
Publication Date: 2014-03-15

Variant appearance in text: F8: I80T
PubMed Link: 24563253
Variant Present in the following documents:
  • Main text
  • 1303142.pdf
View BVdb publication page