BRCA1 c.3003_3004insT ;(p.N1002*)

Variant ID: 17-41244544-T-TA

NM_007294.3(BRCA1):c.3003_3004insT;(p.N1002*)

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: N/A
PubMed Link: 26023681
Variant Present in the following documents:
View BVdb publication page