CDC27 c.1831T>C ;(p.F611L)

Variant ID: 17-45214600-A-G

NM_001256.3(CDC27):c.1831T>C;(p.F611L)

This variant was identified in 12 publications

View GRCh38 version.




Publications:


Whole exome sequencing identified a novel POT1 variant as a candidate pathogenic allele underlying a Li-Fraumeni-like family.

Frontiers In Oncology
Li, Yuping Y; Xie, Yupeng Y; Wang, Di D; Xu, Hanyan H; Ye, Junru J; Yin, Jiani C JC; Chen, Junjie J; Yan, Junrong J; Ye, Bin B; Chen, Chengshui C
Publication Date: 2022

Variant appearance in text: CDC27: 1831T>C; F611L
PubMed Link: 36387164
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08

Variant appearance in text: CDC27: F611L; rs112627286
PubMed Link: 33420045
Variant Present in the following documents:
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
  • 41540_2020_161_MOESM3_ESM.xlsx, sheet 6
View BVdb publication page



KIAA1109 gene mutation in surviving patients with Alkuraya-Kučinskas syndrome: a review of literature.

Bmc Medical Genetics
Kumar, Kishore K; Bellad, Anikha A; Prasad, Pramada P; Girimaji, Satish Chandra SC; Muthusamy, Babylakshmi B
Publication Date: 2020-06-26

Variant appearance in text: CDC27: F611L
PubMed Link: 32590954
Variant Present in the following documents:
  • 12881_2020_1074_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer.

Frontiers In Genetics
Glentis, Stavros S; Dimopoulos, Alexandros C AC; Rouskas, Konstantinos K; Ntritsos, George G; Evangelou, Evangelos E; Narod, Steven A SA; Mes-Masson, Anne-Marie AM; Foulkes, William D WD; Rivera, Barbara B; Tonin, Patricia N PN; Ragoussis, Jiannis J; Dimas, Antigone S AS
Publication Date: 2019

Variant appearance in text: rs112627286
PubMed Link: 31681433
Variant Present in the following documents:
  • DataSheet_1.xlsx, sheet 10
View BVdb publication page



Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer.

Translational Oncology
Ferreira, Elisa Napolitano EN; Brianese, Rafael Canfield RC; de Almeida, Renan Valieris Bueno RVB; Drummond, Rodrigo Duarte RD; de Souza, Jorge Estefano JE; da Silva, Israel Tojal IT; de Souza, Sandro José SJ; Carraro, Dirce Maria DM
Publication Date: 2019-11

Variant appearance in text: rs112627286
PubMed Link: 31419696
Variant Present in the following documents:
  • mmc1.xlsx, sheet 3
View BVdb publication page



Tumor mutation burden and recurrent tumors in hereditary lung cancer.

Cancer Medicine
Hsu, Yi-Chiung YC; Chang, Ya-Hsuan YH; Chang, Gee-Chen GC; Ho, Bing-Ching BC; Yuan, Shin-Sheng SS; Li, Yu-Cheng YC; Zeng, Jhih-Wun JW; Yu, Sung-Liang SL; Li, Ker-Chau KC; Yang, Pan-Chyr PC; Chen, Hsuan-Yu HY
Publication Date: 2019-05

Variant appearance in text: CDC27: F611L; rs112627286
PubMed Link: 30941903
Variant Present in the following documents:
  • CAM4-8-2179-s001.xlsx, sheet 2
View BVdb publication page



PRIMA-1MET-induced neuroblastoma cell death is modulated by p53 and mycn through glutathione level.

Journal Of Experimental & Clinical Cancer Research : Cr
Mlakar, Vid V; Jurkovic Mlakar, Simona S; Lesne, Laurence L; Marino, Denis D; Rathi, Komal S KS; Maris, John M JM; Ansari, Marc M; Gumy-Pause, Fabienne F
Publication Date: 2019-02-12

Variant appearance in text: N/A
PubMed Link: 30755224
Variant Present in the following documents:
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs112627286
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One
Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F
Publication Date: 2015

Variant appearance in text: CDC27: F611L; rs112627286
PubMed Link: 25905921
Variant Present in the following documents:
  • pone.0123569.s008.xls, sheet 7
  • pone.0123569.s008.xls, sheet 11
  • pone.0123569.s008.xls, sheet 4
  • pone.0123569.s008.xls, sheet 8
  • pone.0123569.s008.xls, sheet 5
  • pone.0123569.s008.xls, sheet 3
  • pone.0123569.s008.xls, sheet 10
  • pone.0123569.s008.xls, sheet 1
  • pone.0123569.s008.xls, sheet 6
  • pone.0123569.s008.xls, sheet 9
  • pone.0123569.s008.xls, sheet 2
View BVdb publication page



Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq data.

Human Genomics
Reimann, Ene E; Kõks, Sulev S; Ho, Xuan Dung XD; Maasalu, Katre K; Märtson, Aare A
Publication Date: 2014-12-11

Variant appearance in text: N/A
PubMed Link: 25496518
Variant Present in the following documents:
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: CDC27: F611L; rs112627286
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines.

Plos One
Chang, Han H; Jackson, Donald G DG; Kayne, Paul S PS; Ross-Macdonald, Petra B PB; Ryseck, Rolf-Peter RP; Siemers, Nathan O NO
Publication Date: 2011

Variant appearance in text: CDC27: F611L
PubMed Link: 21701589
Variant Present in the following documents:
  • pone.0021097.s002.xls, sheet 6
  • pone.0021097.s002.xls, sheet 1
  • pone.0021097.s002.xls, sheet 4
View BVdb publication page