BRCA2 c.1461A>T ;(p.A487=)

Variant ID: 13-32907076-A-T

NM_000059.3(BRCA2):c.1461A>T;(p.A487=)

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:

Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair.

Scientific Reports
van de Vrugt, Henri J HJ; Harmsen, Tim T; Riepsaame, Joey J; Alexantya, Georgina G; van Mil, Saskia E SE; de Vries, Yne Y; Bin Ali, Rahmen R; Huijbers, Ivo J IJ; Dorsman, Josephine C JC; Wolthuis, Rob M F RMF; Te Riele, Hein H
Publication Date: 2019-01-25

Variant appearance in text: FANCD1: 1461A>T
PubMed Link: 30683899
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_36506.pdf
View BVdb publication page