CD4 c.1157_1215del ;(p.V386Gfs*36)

Variant ID: 12-6927587-GTTCTGCCCACATGGTCCACCCCGGTGCAGCCAATGGCCCTGATTGTGCTGGGGGGCGTC-G

NM_000616.4(CD4):c.1157_1215del;(p.V386Gfs*36)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Complete Multilineage CD4 Expression Defect Associated With Warts Due to an Inherited Homozygous CD4 Gene Mutation.

Frontiers In Immunology
Fernandes, Rosa Anita RA; Perez-Andres, Martin M; Blanco, Elena E; Jara-Acevedo, Maria M; Criado, Ignacio I; Almeida, Julia J; Botafogo, Vitor V; Coutinho, Ines I; Paiva, Artur A; van Dongen, Jacques J M JJM; Orfao, Alberto A; Faria, Emilia E
Publication Date: 2019

Variant appearance in text: CD4: 1157_1278del
PubMed Link: 31781092
Variant Present in the following documents:
  • Main text
  • fimmu-10-02502.pdf
View BVdb publication page