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APC c.40G>T ;(p.E14*)
Variant ID: 5-112090627-G-T
NM_000038.5(
APC
):c.40G>T;(p.E14*)
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:
Validation and adaptation of the Charlson Comorbidity Index using administrative data from the Colombian health system: retrospective cohort study.
Bmj Open
Oliveros, Henry H; Buitrago, Giancarlo G
Publication Date: 2022-03-23
Variant appearance in text: APC: E14*
PubMed Link:
35321892
Variant Present in the following documents:
bmjopen-2021-054058.draft_revisions.pdf
View BVdb publication page
Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations.
Oncotarget
Porkka, Noora N; Valo, Satu S; Nieminen, Taina T TT; Olkinuora, Alisa A; Mäki-Nevala, Satu S; Eldfors, Samuli S; Peltomäki, Päivi P
Publication Date: 2017-12-08
Variant appearance in text: APC: E14*
PubMed Link:
29296220
Variant Present in the following documents:
oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page