Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRCA2 c.3096_3111del ;(p.K1032Nfs*6)
Variant ID: 13-32911584-TCAAAGATATTGAAGAA-T
NM_000059.3(
BRCA2
):c.3096_3111del;(p.K1032Nfs*6)
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:
Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test.
Cancer Research And Treatment
Shin, Hee-Chul HC; Lee, Han-Byoel HB; Yoo, Tae-Kyung TK; Lee, Eun-Shin ES; Kim, Ryong Nam RN; Park, Boyoung B; Yoon, Kyong-Ah KA; Park, Charny C; Lee, Eun Sook ES; Moon, Hyeong-Gon HG; Noh, Dong-Young DY; Kong, Sun-Young SY; Han, Wonshik W
Publication Date: 2020-07
Variant appearance in text: BRCA2: 3096_3111del; Lys1032Asnfs*6
PubMed Link:
32019277
Variant Present in the following documents:
Main text
crt-2019-559.pdf
View BVdb publication page