KNL1 NM_144508.5(KNL1):c.6212+5G>A

CI-VAR-00071677Explore in graph →NM_144508.5:c.6212+5G>AClinVar 445492 rs115900739

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
445492	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Microcephaly 4, primary, autosomal recessive; Uterine corpus endometrial carcinoma; Sarcoma; Acute myeloid leukemia; Malignant tumor of esophagus; Cervical cancer; Colorectal cancer	germline	6	Dec 11, 2020	clinvar