BRCA2 c.6187_6189delinsTGT ;(p.G2063C)

Variant ID: 13-32914679-GGA-TGT

NM_000059.3(BRCA2):c.6187_6189delinsTGT;(p.G2063C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Scientific Reports
Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE
Publication Date: 2017-04-25

Variant appearance in text: BRCA2: G2063C
PubMed Link: 28440294
Variant Present in the following documents:
  • Main text
View BVdb publication page