PNPT1 NM_033109.5(PNPT1):c.1285-4del

CI-VAR-00236029Explore in graph →NM_033109.5:c.1285-4delClinVar 1541460 rs745754666

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
1541460	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Combined oxidative phosphorylation defect type 13; Autosomal recessive nonsyndromic hearing loss 70; Glioma susceptibility 1; Cholangiocarcinoma; Familial cancer of breast; Gastric cancer; Adrenocortical carcinoma, hereditary; Uterine corpus endometrial carcinoma; Uveal melanoma	germline	4	Jan 28, 2026	clinvar