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APC c.3985C>T ;(p.H1329Y)
Variant ID: 5-112175276-C-T
NM_000038.5(
APC
):c.3985C>T;(p.H1329Y)
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022
Variant appearance in text: APC: H1329Y
PubMed Link:
36072793
Variant Present in the following documents:
Table_3.xlsx, sheet 1
View BVdb publication page
A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes.
Journal Of Cancer
Moniz, Camila Motta Venchiarutti CMV; Riechelmann, Rachel Pimenta RP; Oliveira, Suilane Coelho Ribeiro SCR; Bariani, Giovanni Mendonça GM; Rivelli, Thomas Giollo TG; Ortega, Cintia C; Pereira, Allan Andresson Lima AAL; Meireles, Sibele Inácio SI; Franco, Rejane R; Chen, Andre A; Bonadio, Renata Colombo RC; Nahas, Caio C; Sabbaga, Jorge J; Coudry, Renata Almeida RA; Braghiroli, Maria Ignez MI; Hoff, Paulo Marcelo PM
Publication Date: 2021
Variant appearance in text: APC: 3985C>T; His1329Tyr
PubMed Link:
34729104
Variant Present in the following documents:
Main text
jcav12p7018.pdf
View BVdb publication page
Genotyping data of routinely processed matched primary/metastatic tumor samples.
Data In Brief
Kotoula, Vassiliki V; Chatzopoulos, Kyriakos K; Papadopoulou, Kyriaki K; Giannoulatou, Eleni E; Koliou, Georgia-Angeliki GA; Karavasilis, Vasilios V; Pazarli, Elissavet E; Pervana, Stavroula S; Kafiri, Georgia G; Tsoulfas, Georgios G; Chrisafi, Sofia S; Sgouramali, Helen H; Papakostas, Pavlos P; Pectasides, Dimitrios D; Hytiroglou, Prodromos P; Pentheroudakis, George G; Fountzilas, George G
Publication Date: 2021-02
Variant appearance in text: APC: 3985C>T; His1329Tyr
PubMed Link:
33365374
Variant Present in the following documents:
mmc1.xlsx, sheet 3
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: H1329Y
PubMed Link:
29296220
Variant Present in the following documents:
oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page