TF c.1978_1979delinsGC ;(p.L660A)

Variant ID: 3-133495998-CT-GC

NM_001063.3(TF):c.1978_1979delinsGC;(p.L660A)

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:

A signature motif mediating selective interactions of BCL11A with the NR2E/F subfamily of orphan nuclear receptors.

Nucleic Acids Research
Chan, Chun Ming CM; Fulton, Joel J; Montiel-Duarte, Cristina C; Collins, Hilary M HM; Bharti, Neetu N; Wadelin, Frances R FR; Moran, Paula M PM; Mongan, Nigel P NP; Heery, David M DM
Publication Date: 2013-11

Variant appearance in text: TF: L660A
PubMed Link: 23975195
Variant Present in the following documents:
  • gkt761.pdf
View BVdb publication page