NDUFA13 NM_015965.7(NDUFA13):c.44dup (p.Tyr16fs)

CI-VAR-00295304Explore in graph →p.Tyr16fsNM_015965.7:c.44dupClinVar 2441769 rs751852332

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
2441769	Likely pathogenic	criteria provided, single submitter	1	Mitochondrial complex I deficiency, nuclear type 28; Hurthle cell carcinoma of thyroid	unknown	1	Oct 05, 2022	clinvar