TMEM126A NM_032273.4(TMEM126A):c.395+5G>A

CI-VAR-00033324Explore in graph →NM_032273.4:c.395+5G>AClinVar 215271 rs115906592

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
215271	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive optic atrophy, OPA7 type; Colon adenocarcinoma; Familial cancer of breast; Acute myeloid leukemia; Uterine corpus endometrial carcinoma	germline	6	Jan 25, 2026	clinvar