BRCA2 c.5235_5236insGC ;(p.S1746Afs*32)

Variant ID: 13-32913727-G-GGC

NM_000059.3(BRCA2):c.5235_5236insGC;(p.S1746Afs*32)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.

Plos One
He, Karen Y KY; Zhao, Yiqing Y; McPherson, Elizabeth W EW; Li, Quan Q; Xia, Fan F; Weng, Chunhua C; Wang, Kai K; He, Max M MM
Publication Date: 2016

Variant appearance in text: BRCA2: Ser1746Alafs
PubMed Link: 27930734
Variant Present in the following documents:
  • Main text
  • pone.0167847.pdf
View BVdb publication page