← Lymphatic Malformation Variant Atlas

PIK3CA E110del

c.328_330del NM_006218.3 PI3K-AKT indel, gain of function

Cancer hotspot Recurrent inframe deletion. COSMIC COSV55874554
Population · gnomAD gnomAD v4
ClinVar Likely pathogenic VCV000995382
Protein region inter-domain region Residue 110 of PIK3CA. UniProt P42336

Position in PIK3CA 14 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 aaR88QE109delE110delN345KC420RE542KE545AE545GE545KQ546KQ546RM1043IH1047LH1047R

Reported in LM

ISSVA subsetAllele fractionSources
LM 1.06-2.70%

Bars show the reported allele-fraction range on a 0 to 50 percent axis.

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. Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
    Brouillard P, Schlögel MJ, Homayun Sepehr N, Helaers R, Queisser A, Fastré E, Boutry S, Schmitz S, Clapuyt P, Hammer F, Dompmartin A, Weitz-Tuoretmaa A, Laranne J, Pasquesoone L, Vilain C, Boon LM, Vikkula M. · Orphanet J Rare Dis · 2021

Mentioned in 27 publications indexed by Europe PMC.

Cross-references