KIAA0586 NM_001329943.3(KIAA0586):c.1097A>T (p.Glu366Val) — variant · CancerIndex

Variant · Snv

KIAA0586 NM_001329943.3(KIAA0586):c.1097A>T (p.Glu366Val)

CI-VAR-00125789Explore in graph →p.Glu366ValNM_001329943.3:c.1097A>TClinVar 707461 rs59248588

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
707461	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Joubert syndrome 23; Short-rib thoracic dysplasia 14 with polydactyly; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Hepatocellular carcinoma	germline	5	Feb 01, 2026	clinvar