KIAA0586 NM_001329943.3(KIAA0586):c.202T>A (p.Ser68Thr)

CI-VAR-00077653Explore in graph →p.Ser68ThrNM_001329943.3:c.202T>AClinVar 475443 rs147119902

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
475443	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Joubert syndrome 23; Short-rib thoracic dysplasia 14 with polydactyly; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma	germline	6	Jan 12, 2026	clinvar