Bibliome.ai browser hg19
Search
About
Stats
FAQ
CD4 c.1147_1148delinsGC ;(p.N383A)
Variant ID: 12-6926487-AA-GC
NM_000616.4(
CD4
):c.1147_1148delinsGC;(p.N383A)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
FoxP3 scanning mutagenesis reveals functional variegation and mild mutations with atypical autoimmune phenotypes.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Kwon, Ho-Keun HK; Chen, Hui-Min HM; Mathis, Diane D; Benoist, Christophe C
Publication Date: 2018-01-09
Variant appearance in text: CD4: N383A
PubMed Link:
29269391
Variant Present in the following documents:
Main text
View BVdb publication page