TET2 c.4361_4362insG ;(p.R1455Qfs*23)

Variant ID: 4-106193899-T-TG

NM_001127208.2(TET2):c.4361_4362insG;(p.R1455Qfs*23)

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:

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.

Breast Cancer Research : Bcr
Li, Na N; Rowley, Simone M SM; Thompson, Ella R ER; McInerny, Simone S; Devereux, Lisa L; Amarasinghe, Kaushalya C KC; Zethoven, Magnus M; Lupat, Richard R; Goode, David D; Li, Jason J; Trainer, Alison H AH; Gorringe, Kylie L KL; James, Paul A PA; Campbell, Ian G IG
Publication Date: 2018-01-09

Variant appearance in text: TET2: 4361_4362insG
PubMed Link: 29316957
Variant Present in the following documents:
  • Main text
  • 13058_2017_Article_929.pdf
View BVdb publication page