TRAPPC11 NM_021942.6(TRAPPC11):c.2851+46G>A

CI-VAR-00200284Explore in graph →NM_021942.6:c.2851+46G>AClinVar 1265498 rs62358033

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
1265498	Benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive limb-girdle muscular dystrophy type R18; Malignant tumor of esophagus; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Gastric cancer; Cholangiocarcinoma	germline	4	Sep 10, 2021	clinvar