Variant · Snv
HADHB NM_000183.3(HADHB):c.1149+4A>T
CI-VAR-00017997Explore in graph →NM_000183.3:c.1149+4A>TClinVar 92597 rs2303893
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 92597 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Mitochondrial trifunctional protein deficiency; Adrenocortical carcinoma, hereditary; Familial cancer of breast; Ovarian cancer; Uveal melanoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Uterine carcinosarcoma; Nonpapillary renal cell carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Lymphoma; Cholangiocarcinoma | germline | 8 | Feb 04, 2026 | clinvar |