TTC32 c.317-49G>T

Variant ID: 2-20096936-C-A

NM_001008237.1(TTC32):c.317-49G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution.

Bmc Cancer
Mosquera Orgueira, Adrián A; Antelo Rodríguez, Beatriz B; Alonso Vence, Natalia N; Díaz Arias, José Ángel JÁ; Díaz Varela, Nicolás N; Pérez Encinas, Manuel Mateo MM; Allegue Toscano, Catarina C; Goiricelaya Seco, Elena María EM; Carracedo Álvarez, Ángel Á; Bello López, José Luis JL
Publication Date: 2019-05-29

Variant appearance in text: rs7563410
PubMed Link: 31142279
Variant Present in the following documents:
  • Main text
  • 12885_2019_Article_5628.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: TTC32: 317-49G>T; rs7563410
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
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: rs7563410
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page