Variant · Snv
KTN1 NM_001079521.2(KTN1):c.1060C>A (p.Arg354=)
CI-VAR-00127176Explore in graph →p.Arg354=NM_001079521.2:c.1060C>AClinVar 779682 rs17128636
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 |
|---|---|---|---|---|---|---|---|---|
| 779682 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Clear cell carcinoma of kidney; Cervical cancer; Colon adenocarcinoma; Sarcoma; Gastric cancer; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Hepatocellular carcinoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 3 | Dec 31, 2019 | clinvar |