TGM1 NM_000359.3(TGM1):c.877-2A>G

CI-VAR-00049559Explore in graph →NM_000359.3:c.877-2A>GClinVar 279911 rs142634031

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
279911	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive congenital ichthyosis 1; Autosomal recessive congenital ichthyosis; TGM1-related disorder; Cholangiocarcinoma; Lamellar ichthyosis; Lung cancer; Familial cancer of breast; Fetal anomalies with a likely genetic cause; Thyroid cancer, nonmedullary, 1	germline	25	May 23, 2026	clinvar