Variant · Snv
THADA NM_022065.5(THADA):c.4059G>T (p.Arg1353Ser)
CI-VAR-00126303Explore in graph →p.Arg1353SerNM_022065.5:c.4059G>TClinVar 770868 rs56269749
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 |
|---|---|---|---|---|---|---|---|---|
| 770868 | Benign | criteria provided, multiple submitters, no conflicts | 2 | THADA-related disorder; Thymoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Lung cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Familial pancreatic carcinoma; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Cervical cancer; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Ovarian cancer | germline | 4 | May 08, 2018 | clinvar |