HR c.1468_1469delinsGC ;(p.L490A)

Variant ID: 8-21983182-AG-GC

NM_005144.4(HR):c.1468_1469delinsGC;(p.L490A)

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:

The orphan nuclear receptor SHP utilizes conserved LXXLL-related motifs for interactions with ligand-activated estrogen receptors.

Molecular And Cellular Biology
Johansson, L L; Båvner, A A; Thomsen, J S JS; Färnegårdh, M M; Gustafsson, J A JA; Treuter, E E
Publication Date: 2000-02

Variant appearance in text: HR: L490A
PubMed Link: 10648597
Variant Present in the following documents:
  • Main text
View BVdb publication page