IFT52 c.208-1705T>C

Variant ID: 20-42230695-T-C

NM_016004.2(IFT52):c.208-1705T>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

MYBL2 alternative splicing-related genetic variants reduce the risk of triple-negative breast cancer in the Chinese population.

Frontiers In Genetics
Chen, Xinyu X; Feng, Jin J; Zhang, Yuan Y; Liu, Jiarui J; Zhang, Lijia L; Zeng, Pu P; Wen, Langbo L; Wang, Xin X; Zhang, Yi Y
Publication Date: 2023

Variant appearance in text: IFT52: 208-1705T>C; rs6073143
PubMed Link: 37144133
Variant Present in the following documents:
  • DataSheet2.xlsx, sheet 1
View BVdb publication page