BRCA2 c.5700_5701insT ;(p.E1901*)

Variant ID: 13-32914192-A-AT

NM_000059.3(BRCA2):c.5700_5701insT;(p.E1901*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Ebiomedicine
Foley, Samantha B SB; Rios, Jonathan J JJ; Mgbemena, Victoria E VE; Robinson, Linda S LS; Hampel, Heather L HL; Toland, Amanda E AE; Durham, Leslie L; Ross, Theodora S TS
Publication Date: 2015-01

Variant appearance in text: BRCA2: E1901fs
PubMed Link: 26023681
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page