HR c.262_263delinsCG ;(p.V88R)

Variant ID: 8-21986421-AC-CG

NM_005144.4(HR):c.262_263delinsCG;(p.V88R)

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:

Base excision repair defects invoke hypersensitivity to PARP inhibition.

Molecular Cancer Research : Mcr
Horton, Julie K JK; Stefanick, Donna F DF; Prasad, Rajendra R; Gassman, Natalie R NR; Kedar, Padmini S PS; Wilson, Samuel H SH
Publication Date: 2014-08

Variant appearance in text: HR: V88R
PubMed Link: 24770870
Variant Present in the following documents:
  • Main text
View BVdb publication page