AQP12B c.386C>G ;(p.T129R)

Variant ID: 2-241621869-G-C

NM_001102467.1(AQP12B):c.386C>G;(p.T129R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-exome sequencing and genome-wide methylation analyses identify novel disease associated mutations and methylation patterns in idiopathic hypereosinophilic syndrome.

Oncotarget
Andersen, Christen Lykkegaard CL; Nielsen, Helene Myrtue HM; Kristensen, Lasse Sommer LS; Søgaard, Alexandra A; Vikeså, Jonas J; Jønson, Lars L; Nielsen, Finn Cilius FC; Hasselbalch, Hans H; Bjerrum, Ole Weis OW; Punj, Vasu V; Grønbæk, Kirsten K
Publication Date: 2015-12-01

Variant appearance in text: rs74882485
PubMed Link: 26497854
Variant Present in the following documents:
  • Main text
  • oncotarget-06-40588.pdf
View BVdb publication page