BRCA2 c.337_339del ;(p.R113del)

Variant ID: 13-32899233-TAGA-T

NM_000059.3(BRCA2):c.337_339del;(p.R113del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing.

Scientific Reports
Wang, Xiaoyuan X; Zhang, Yanqin Y; Ding, Jie J; Wang, Fang F
Publication Date: 2021-09-10

Variant appearance in text: BRCA2: r113del
PubMed Link: 34508137
Variant Present in the following documents:
  • 41598_2021_Article_97414.pdf
View BVdb publication page