Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRCA2 c.442_443delinsGC ;(p.C148A)
Variant ID: 13-32900254-TG-GC
NM_000059.3(
BRCA2
):c.442_443delinsGC;(p.C148A)
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:
Intrinsic Disorder and Phosphorylation in BRCA2 Facilitate Tight Regulation of Multiple Conserved Binding Events.
Biomolecules
Julien, Manon M; Ghouil, Rania R; Petitalot, Ambre A; Caputo, Sandrine M SM; Carreira, Aura A; Zinn-Justin, Sophie S
Publication Date: 2021-07-20
Variant appearance in text: BRCA2: C148A
PubMed Link:
34356684
Variant Present in the following documents:
Main text
biomolecules-11-01060.pdf
View BVdb publication page