SAMD9 NM_017654.4(SAMD9):c.4001G>T (p.Arg1334Ile)

CI-VAR-00203448Explore in graph →p.Arg1334IleNM_017654.4:c.4001G>TClinVar 1336034 rs141248575

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
1336034	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Monosomy 7 myelodysplasia and leukemia syndrome 2; Inborn genetic diseases; MIRAGE syndrome; Normophosphatemic familial tumoral calcinosis	germline	6	Jan 14, 2026	clinvar