COL4A3 NM_000091.5(COL4A3):c.1576-15T>G

CI-VAR-00047078Explore in graph →NM_000091.5:c.1576-15T>GClinVar 254984 rs56243460

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
254984	Benign	criteria provided, multiple submitters, no conflicts	2	Alport syndrome; Autosomal recessive Alport syndrome; Thymoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma; Ovarian serous cystadenocarcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Lymphoma	germline	9	Feb 04, 2026	clinvar