TMEM147 NM_032635.4(TMEM147):c.345-1G>T

CI-VAR-00242008Explore in graph →NM_032635.4:c.345-1G>TClinVar 1708024 rs566519921

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
1708024	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-pelger-huet anomaly; Gastric cancer	germline	3	Feb 23, 2023	clinvar