TF c.39C>G ;(p.V13=)

Variant ID: 3-133465323-C-G

NM_001063.3(TF):c.39C>G;(p.V13=)

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:

Prediction of nuclear proteins using nuclear translocation signals proposed by probabilistic latent semantic indexing.

Bmc Bioinformatics
Su, Emily Chia-Yu EC; Chang, Jia-Ming JM; Cheng, Cheng-Wei CW; Sung, Ting-Yi TY; Hsu, Wen-Lian WL
Publication Date: 2012

Variant appearance in text: TF: V13V
PubMed Link: 23282098
Variant Present in the following documents:
  • 1471-2105-13-S17-S13.pdf
View BVdb publication page