BRCA2 c.2989_2990insAA ;(p.L997*)

Variant ID: 13-32911481-T-TAA

NM_000059.3(BRCA2):c.2989_2990insAA;(p.L997*)

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:

Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection.

Familial Cancer
van Harssel, J J T JJ; van Roozendaal, C E P CE; Detisch, Y Y; Brandão, R D RD; Paulussen, A D C AD; Zeegers, M M; Blok, M J MJ; Gómez García, E B EB
Publication Date: 2010-06

Variant appearance in text: BRCA2: 2989_2990insAA
PubMed Link: 19949876
Variant Present in the following documents:
  • Main text
  • 10689_2009_Article_9305.pdf
View BVdb publication page