← Lymphatic Malformation Variant Atlas

PIK3CA E109del

c.325_327delGAA NM_006218.3 PI3K-AKT indel, gain of function

Cancer hotspot Recurrent inframe deletion. COSMIC COSV55874554
Population · gnomAD gnomAD v4
ClinVar Not in ClinVar no exact-match submission
Protein region inter-domain region Residue 109 of PIK3CA. UniProt P42336

Position in PIK3CA 15 catalogued

PI3K-ABD (16–105)PI3K-ABDPI3K-RBD (187–289)PI3K-RBDC2 PI3K-type (330–487)C2 PI3K-typePIK helical (517–694)PIK helicalPI3K/PI4K catalytic (765–1051)PI3K/PI4K ca…11068 aaR88QE109delE110delN345KC420RP447_L455delE542KE545AE545GE545KQ546KQ546RM1043IH1047LH1047R

Reported in LM

ISSVA subsetAllele fractionSources
LM n.r. (LEC line; Sanger, not quantified)

Pathway and targeted therapy

Driver of the PI3K-AKT pathway. Repurposed drugs already used in the clinic for this pathway: alpelisib (PI3Kα inhibitor), sirolimus (mTOR inhibitor).

Open and recent trials (3 in vascular / lymphatic anomalies for alpelisib)

Primary sources (1)

  1. PIK3CA mutations are specifically localized to lymphatic endothelial cells of lymphatic malformations.
    Blesinger H, Kaulfuß S, Aung T, Schwoch S, Prantl L, Rößler J, Wilting J, Becker J. · PLoS One · 2018

Mentioned in 6 publications indexed by Europe PMC.

Cross-references