BRCA2 c.577_579delinsGAG ;(p.S193E)

Variant ID: 13-32900696-TCT-GAG

NM_000059.3(BRCA2):c.577_579delinsGAG;(p.S193E)

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: S193E
PubMed Link: 34356684
Variant Present in the following documents:
  • Main text
  • biomolecules-11-01060.pdf
View BVdb publication page