PTEN c.409_411delinsTTT ;(p.A137F)

Variant ID: 10-89692925-GCA-TTT

NM_000314.4(PTEN):c.409_411delinsTTT;(p.A137F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022

Variant appearance in text: rs878853938
PubMed Link: 36561320
Variant Present in the following documents:
  • Table2.xlsx, sheet 6
View BVdb publication page



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: A137F
PubMed Link: 31819097
Variant Present in the following documents:
  • Main text
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
  • 41598_2019_Article_54976.pdf
View BVdb publication page