TMEM127 NM_017849.4(TMEM127):c.24_32del (p.Leu9_Gly11del) — variant · CancerIndex

Variant · Deletion

TMEM127 NM_017849.4(TMEM127):c.24_32del (p.Leu9_Gly11del)

CI-VAR-00160031Explore in graph →p.Leu9_Gly11delNM_017849.4:c.24_32delClinVar 951046 rs1684396239

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
951046	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Hereditary pheochromocytoma and paraganglioma; Hereditary cancer-predisposing syndrome; Pheochromocytoma	germline	3	May 05, 2025	clinvar