Variant · Snv
HNRNPH1 NM_001257293.2(HNRNPH1):c.-31-6T>G
CI-VAR-00384346Explore in graph →NM_001257293.2:c.-31-6T>GClinVar 3904784
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 |
|---|---|---|---|---|---|---|---|---|
| 3904784 | Likely benign | criteria provided, single submitter | 1 | Acute myeloid leukemia; Malignant tumor of urinary bladder; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Papillary renal cell carcinoma type 1; Cholangiocarcinoma; Lung cancer; Familial cancer of breast; Thymoma; Melanoma; Cervical cancer; Ovarian cancer | germline | 2 | Feb 01, 2026 | clinvar |