COL4A5 NM_033380.3(COL4A5):c.438+36G>T

CI-VAR-00170163Explore in graph →NM_033380.3:c.438+36G>TClinVar 994005 rs73526282

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
994005	Benign	criteria provided, multiple submitters, no conflicts	2	X-linked Alport syndrome; Sarcoma; Ovarian serous cystadenocarcinoma; Gastric cancer; Acute myeloid leukemia	germline	3	Jan 21, 2020	clinvar