Variant · Snv
DROSHA NM_001382508.1(DROSHA):c.1669G>T (p.Ala557Ser)
CI-VAR-00339151Explore in graph →p.Ala557SerNM_001382508.1:c.1669G>TClinVar 3050303 rs61751194
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 |
|---|---|---|---|---|---|---|---|---|
| 3050303 | Likely benign | no assertion criteria provided | 0 | DROSHA-related disorder; Uterine corpus endometrial carcinoma; Acute myeloid leukemia; Lung cancer; Cervical cancer; Clear cell carcinoma of kidney; Familial cancer of breast; Familial pancreatic carcinoma; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Melanoma; Malignant tumor of esophagus | germline | 2 | Jul 03, 2020 | clinvar |