NYNRIN c.3761G>A ;(p.W1254*)

Variant ID: 14-24884716-G-A

NM_025081.2(NYNRIN):c.3761G>A;(p.W1254*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of new Wilms tumour predisposition genes: an exome sequencing study.

The Lancet. Child & Adolescent Health
Mahamdallie, Shazia S; Yost, Shawn S; Poyastro-Pearson, Emma E; Holt, Esty E; Zachariou, Anna A; Seal, Sheila S; Elliott, Anna A; Clarke, Matthew M; Warren-Perry, Margaret M; Hanks, Sandra S; Anderson, John J; Bomken, Simon S; Cole, Trevor T; Farah, Roula R; Furtwaengler, Rhoikos R; Glaser, Adam A; Grundy, Richard R; Hayden, James J; Lowis, Steve S; Millot, Frédéric F; Nicholson, James J; Ronghe, Milind M; Skeen, Jane J; Williams, Denise D; Yeomanson, Daniel D; Ruark, Elise E; Rahman, Nazneen N
Publication Date: 2019-05

Variant appearance in text: NYNRIN: Trp1254X
PubMed Link: 30885698
Variant Present in the following documents:
  • Main text
  • mmc1.pdf
  • main.pdf
View BVdb publication page