CREBBP c.188_189inv ;(p.A63E)

Variant ID: 16-3900907-AG-CT

NM_004380.2(CREBBP):c.188_189inv;(p.A63E)

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:

Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome.

Cell
Greenberg, Rachel S RS; Long, Hannah K HK; Swigut, Tomek T; Wysocka, Joanna J
Publication Date: 2019-09-05

Variant appearance in text: CREBBP: A63E
PubMed Link: 31491386
Variant Present in the following documents:
  • Main text
View BVdb publication page