PTEN c.308_309delinsAA ;(p.P103Q)

Variant ID: 10-89692824-CC-AA

NM_000314.4(PTEN):c.308_309delinsAA;(p.P103Q)

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:

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: P103Q
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