Variant · Snv
SPATA7 NM_018418.5(SPATA7):c.191-14C>A
CI-VAR-00052567Explore in graph →NM_018418.5:c.191-14C>AClinVar 314776 rs60770744
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 |
|---|---|---|---|---|---|---|---|---|
| 314776 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Leber congenital amaurosis 3; Retinitis pigmentosa; Cervical cancer; Gastric cancer; Acute myeloid leukemia; Lung cancer; Uterine corpus endometrial carcinoma; Sarcoma; Thymoma; Malignant tumor of esophagus | germline | 4 | Feb 04, 2026 | clinvar |