Variant · Snv
IQGAP3 NM_178229.5(IQGAP3):c.3976+5G>A
CI-VAR-00339170Explore in graph →NM_178229.5:c.3976+5G>AClinVar 3056368 rs41267377
Curated evidence
Evidence by cancer (0 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.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3056368 | Benign | no assertion criteria provided | 0 | IQGAP3-related disorder; Colorectal cancer; Gastric cancer; Nonpapillary renal cell carcinoma; Uterine carcinosarcoma; Lung cancer; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Familial pancreatic carcinoma; Colon adenocarcinoma; Ovarian cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Cervical cancer | germline | 2 | Feb 26, 2019 | clinvar |