SLX4 NM_032444.4(SLX4):c.5248_5249delinsTT (p.Ala1750Leu) — variant · CancerIndex

Variant · Indel

SLX4 NM_032444.4(SLX4):c.5248_5249delinsTT (p.Ala1750Leu)

CI-VAR-00044819Explore in graph →p.Ala1750LeuNM_032444.4:c.5248_5249delinsTTClinVar 241695 rs878855163

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
241695	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Fanconi anemia; Fanconi anemia complementation group P	germline	2	Oct 29, 2024	clinvar