MYO18B NM_032608.7(MYO18B):c.7537G>A (p.Gly2513Ser)

CI-VAR-00199777Explore in graph →p.Gly2513SerNM_032608.7:c.7537G>AClinVar 1249400 rs7284177

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
1249400	Benign	criteria provided, multiple submitters, no conflicts	2	Colon adenocarcinoma; Gastric cancer; Uterine carcinosarcoma; Acute myeloid leukemia; Sarcoma; Ovarian serous cystadenocarcinoma	germline	4	Feb 03, 2026	clinvar