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BRCA2 c.1633_1635delinsATG ;(p.V545M)
Variant ID: 13-32907248-GTT-ATG
NM_000059.3(
BRCA2
):c.1633_1635delinsATG;(p.V545M)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.
Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31
Variant appearance in text: BRCA2: V545M
PubMed Link:
33384420
Variant Present in the following documents:
Main text
View BVdb publication page