CFI NM_000204.5(CFI):c.772G>A (p.Ala258Thr)

CI-VAR-00214761Explore in graph →p.Ala258ThrNM_000204.5:c.772G>AClinVar 1451295 rs199688124

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
1451295	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Factor I deficiency; Age related macular degeneration 13; Atypical hemolytic-uremic syndrome with I factor anomaly; CFI-related disorder; Colon adenocarcinoma	germline	13	Aug 10, 2026	clinvar