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BRCA2 c.5235_5236insGC ;(p.S1746Afs*32)
Variant ID: 13-32913727-G-GGC
NM_000059.3(
BRCA2
):c.5235_5236insGC;(p.S1746Afs*32)
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:
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.
Plos One
He, Karen Y KY; Zhao, Yiqing Y; McPherson, Elizabeth W EW; Li, Quan Q; Xia, Fan F; Weng, Chunhua C; Wang, Kai K; He, Max M MM
Publication Date: 2016
Variant appearance in text: BRCA2: Ser1746Alafs
PubMed Link:
27930734
Variant Present in the following documents:
Main text
pone.0167847.pdf
View BVdb publication page