CP c.782-14C>T

Variant ID: 3-148925418-G-A

NM_000096.3(CP):c.782-14C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.

Frontiers In Genetics
Simba, Hannah H; Kuivaniemi, Helena H; Lutje, Vittoria V; Tromp, Gerard G; Sewram, Vikash V
Publication Date: 2019

Variant appearance in text: rs34067682
PubMed Link: 31428123
Variant Present in the following documents:
  • Main text
  • fgene-10-00642.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: CP: 782-14C>T; rs34067682
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.

Parkinson'S Disease
Castiglioni, Emanuela E; Finazzi, Dario D; Goldwurm, Stefano S; Pezzoli, Gianni G; Forni, Gianluca G; Girelli, Domenico D; Maccarinelli, Federica F; Poli, Maura M; Ferrari, Maurizio M; Cremonesi, Laura L; Arosio, Paolo P
Publication Date: 2010-10-17

Variant appearance in text: rs34067682
PubMed Link: 20981230
Variant Present in the following documents:
  • Main text
  • PD2011-827693.pdf
View BVdb publication page