COL4A5 NM_033380.3(COL4A5):c.2349G>A (p.Pro783=)

CI-VAR-00006555Explore in graph →p.Pro783=NM_033380.3:c.2349G>AClinVar 24511 rs3747408

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
24511	Benign	criteria provided, multiple submitters, no conflicts	2	X-linked Alport syndrome; Hepatocellular carcinoma; Ovarian cancer; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Sarcoma; Uterine carcinosarcoma; Thymoma	germline	11	Feb 04, 2026	clinvar