PTEN c.406T>G ;(p.C136G)

Variant ID: 10-89692922-T-G

NM_000314.4(PTEN):c.406T>G;(p.C136G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: PTEN: C136G
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Genomic profiling in ovarian cancer retreated with platinum based chemotherapy presented homologous recombination deficiency and copy number imbalances of CCNE1 and RB1 genes.

Bmc Cancer
da Costa, Alexandre A B A AABA; do Canto, Luisa M LM; Larsen, Simon Jonas SJ; Ribeiro, Adriana Regina Gonçalves ARG; Stecca, Carlos Eduardo CE; Petersen, Annabeth Høgh AH; Aagaard, Mads M MM; de Brot, Louise L; Baumbach, Jan J; Baiocchi, Glauco G; Achatz, Maria Isabel MI; Rogatto, Silvia Regina SR
Publication Date: 2019-05-06

Variant appearance in text: PTEN: c136G
PubMed Link: 31060523
Variant Present in the following documents:
  • Main text
  • 12885_2019_Article_5622.pdf
View BVdb publication page