BRCA2 c.2190_2191insT ;(p.E731*)

Variant ID: 13-32910682-A-AT

NM_000059.3(BRCA2):c.2190_2191insT;(p.E731*)

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:

Germline and somatic mutations in homologous recombination genes among Chinese ovarian cancer patients detected using next-generation sequencing.

Journal Of Gynecologic Oncology
Zhao, Qianying Q; Yang, Jiaxin J; Li, Lei L; Cao, Dongyan D; Yu, Mei M; Shen, Keng K; ,
Publication Date: 2017-07

Variant appearance in text: BRCA2: Glu731fs
PubMed Link: 28541631
Variant Present in the following documents:
  • Main text
  • jgo-28-e39.pdf
View BVdb publication page