BRCA2 c.3852dup ;(p.E1285*)

Variant ID: 13-32912343-G-GT

NM_000059.3(BRCA2):c.3852dup;(p.E1285*)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.

Journal Of Genetic Counseling
Amendola, Laura M LM; Hart, M Ragan MR; Bennett, Robin L RL; Horike-Pyne, Martha M; Dorschner, Michael M; Shirts, Brian B; Jarvik, Gail P GP
Publication Date: 2019-12

Variant appearance in text: N/A
PubMed Link: 31317629
Variant Present in the following documents:
View BVdb publication page