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APC c.1152_1153insCC ;(p.A385Pfs*70)
Variant ID: 5-112154881-T-TCC
NM_000038.5(
APC
):c.1152_1153insCC;(p.A385Pfs*70)
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:
Comprehensive analysis of germline mutations in northern Brazil: a panel of 16 genes for hereditary cancer-predisposing syndrome investigation.
Bmc Cancer
Vidal, Amanda Ferreira AF; Ferraz, Rafaella Sousa RS; El-Husny, Antonette A; Silva, Caio Santos CS; Vinasco-Sandoval, Tatiana T; Magalhães, Leandro L; Raiol-Moraes, Milene M; Barra, Williams Fernandes WF; Pereira, Cynthia Lara Brito Lins CLBL; de Assumpção, Paulo Pimentel PP; de Brito, Leonardo Miranda LM; Vialle, Ricardo Assunção RA; Santos, Sidney S; Ribeiro-Dos-Santos, Ândrea Â; Ribeiro-Dos-Santos, André M AM
Publication Date: 2021-04-07
Variant appearance in text: APC: Ala385Profs
PubMed Link:
33827469
Variant Present in the following documents:
Main text
12885_2021_Article_8089.pdf
View BVdb publication page