Variant · Snv
ACTR1B NM_005735.4(ACTR1B):c.333G>A (p.Thr111=)
CI-VAR-00306082Explore in graph →p.Thr111=NM_005735.4:c.333G>AClinVar 2651171 rs142996046
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 |
|---|---|---|---|---|---|---|---|---|
| 2651171 | Likely benign | criteria provided, single submitter | 1 | Uterine corpus endometrial carcinoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Lymphoma; Uterine carcinosarcoma; Hepatocellular carcinoma; Cervical cancer; Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Sarcoma | germline | 2 | Apr 01, 2023 | clinvar |