Variant · Snv
AKT1 E17K
CI-VAR-00000677Explore in graph →NP_001014432.1:p.Glu17LysNM_001014432.1:c.49G>AClinVar 13983 CIViC 4 rs121434592 rs34409589
Curated evidence
Evidence by cancer (8 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 23888070
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Breast Neoplasm2 | ||||||||
| AKT1 E17K | Akt Inhibitor MK2206 | Predictive | D | Does Not Support Sensitivity Response | 3 | accepted | EID231Breast cancer cell lines with the AKT1 E17K mutation did not show sensitivity to AKT inhibitor MK-2206, unlike cell lines with PIK3CA mutations. PMID 23888070 · Beaver et al., 2013 · Open in CIViC | civic |
| AKT1 E17K | Capivasertib | Predictive | C | Supports Sensitivity Response | 3 | accepted | EID709In a phase-I study of AZD5363, partial response was observed in 2 patients with breast and ovarian carcinoma, respectively, and AKT1 E17K mutations. While full study results have not yet been publishe… (full text at CIViC) PMID 26351323 · Davies et al., 2015 · Open in CIViC | civic |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 13983 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Breast adenocarcinoma; Carcinoma of colon; Ovarian neoplasm; Proteus syndrome; Cowden syndrome 6; Neoplasm; Meningioma; Medulloblastoma SHH activated and TP53 wild-type; Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype | germline/somatic | 9 | Apr 15, 2026 |