TSHR NM_000369.5(TSHR):c.1377G>A (p.Ala459=)

CI-VAR-00047479Explore in graph →p.Ala459=NM_000369.5:c.1377G>AClinVar 255951 rs113951800

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
255951	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hypothyroidism due to TSH receptor mutations; Familial hyperthyroidism due to mutations in TSH receptor; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Gastric cancer; Thymoma; Cervical cancer; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma	germline	8	May 12, 2026	clinvar