BRCA2 c.4631_4632insG ;(p.N1544Kfs*4)

Variant ID: 13-32913123-A-AG

NM_000059.3(BRCA2):c.4631_4632insG;(p.N1544Kfs*4)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank.

Genome Medicine
Abul-Husn, Noura S NS; Soper, Emily R ER; Odgis, Jacqueline A JA; Cullina, Sinead S; Bobo, Dean D; Moscati, Arden A; Rodriguez, Jessica E JE; , ; , ; Loos, Ruth J F RJF; Cho, Judy H JH; Belbin, Gillian M GM; Suckiel, Sabrina A SA; Kenny, Eimear E EE
Publication Date: 2019-12-31

Variant appearance in text: BRCA2: 4631_4632insG; Asn1544fs
PubMed Link: 31892343
Variant Present in the following documents:
  • 13073_2019_691_MOESM1_ESM.pdf
View BVdb publication page