F8 c.500C>G ;(p.A167G)

Variant ID: X-154221312-G-C

NM_000132.3(F8):c.500C>G;(p.A167G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: A167G
PubMed Link: 24563253
Variant Present in the following documents:
  • Main text
  • 1303142.pdf
View BVdb publication page