RET NM_020975.6(RET):c.1142T>G (p.Phe381Cys)

CI-VAR-00274174Explore in graph →p.Phe381CysNM_020975.6:c.1142T>GClinVar 2178070 rs139813765

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
2178070	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Multiple endocrine neoplasia, type 2; Familial medullary thyroid carcinoma; Hereditary cancer-predisposing syndrome; Multiple endocrine neoplasia type 2B; Hirschsprung disease, susceptibility to, 1; Multiple endocrine neoplasia type 2A; Pheochromocytoma	germline	4	Dec 05, 2024	clinvar