UTP4 NM_032830.3(UTP4):c.1164+8A>G

CI-VAR-00127982Explore in graph →NM_032830.3:c.1164+8A>GClinVar 717483 rs112053857

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
717483	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary North American Indian childhood cirrhosis; UTP4-related disorder; Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Lung cancer	germline	4	Jan 22, 2026	clinvar