TMEM131L NM_001131007.2(TMEM131L):c.1061C>T (p.Ala354Val) — variant · CancerIndex

Variant · Snv

TMEM131L NM_001131007.2(TMEM131L):c.1061C>T (p.Ala354Val)

CI-VAR-00343236Explore in graph →p.Ala354ValNM_001131007.2:c.1061C>TClinVar 3178590 rs375611056

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
3178590	Uncertain significance	criteria provided, single submitter	1	Familial pancreatic carcinoma	germline	2	Dec 16, 2025	clinvar