BRCA2 c.7435+7T>G

Variant ID: 13-32929432-T-G

NM_000059.3(BRCA2):c.7435+7T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


APPLICATION OF THE ACMG/AMP FRAMEWORK TO CAPTURE EVIDENCE RELEVANT TO PREDICTED AND OBSERVED IMPACT ON SPLICING: RECOMMENDATIONS FROM THE CLINGEN SVI SPLICING SUBGROUP.

Medrxiv : The Preprint Server For Health Sciences
Walker, Logan C LC; de la Hoya, Miguel M; Wiggins, George Ar GA; Lindy, Amanda A; Vincent, Lisa M LM; Parsons, Michael M; Canson, Daffodil M DM; Bis-Brewer, Dana D; Cass, Ashley A; Tchourbanov, Alexander A; Zimmermann, Heather H; Byrne, Alicia B AB; Pesaran, Tina T; Karam, Rachid R; Harrison, Steven M SM; , ; Spurdle, Amanda B AB
Publication Date: 2023-02-26

Variant appearance in text: BRCA2: 7435+7T>G
PubMed Link: 36865205
Variant Present in the following documents:
  • media-10.xlsx, sheet 1
  • media-8.xlsx, sheet 1
View BVdb publication page



Minigene Splicing Assays Identify 12 Spliceogenic Variants of BRCA2 Exons 14 and 15.

Frontiers In Genetics
Fraile-Bethencourt, Eugenia E; Valenzuela-Palomo, Alberto A; Díez-Gómez, Beatriz B; Caloca, María José MJ; Gómez-Barrero, Susana S; Velasco, Eladio A EA
Publication Date: 2019

Variant appearance in text: BRCA2: 7435+7T>G
PubMed Link: 31191615
Variant Present in the following documents:
  • Main text
  • fgene-10-00503.pdf
View BVdb publication page