Variant · Snv
DHX34 NM_014681.6(DHX34):c.2999G>A (p.Arg1000Gln)
CI-VAR-00338638Explore in graph →p.Arg1000GlnNM_014681.6:c.2999G>AClinVar 3038245 rs142828801
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3038245 | Likely benign | criteria provided, single submitter | 1 | DHX34-related disorder; Clear cell carcinoma of kidney; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Hepatocellular carcinoma; Lung cancer; Familial cancer of breast; Melanoma; Malignant tumor of urinary bladder | germline | 3 | May 01, 2026 | clinvar |