PRPS1 NM_002764.4(PRPS1):c.641G>A (p.Arg214Gln)

CI-VAR-00202314Explore in graph →p.Arg214GlnNM_002764.4:c.641G>AClinVar 1320158 rs867288458

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
1320158	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Arts syndrome; Charcot-Marie-Tooth Neuropathy X; Retinal dystrophy; Hearing loss, X-linked 1; Charcot-Marie-Tooth disease X-linked recessive 5; Phosphoribosylpyrophosphate synthetase superactivity; Thyroid cancer, nonmedullary, 1	germline	7	Mar 14, 2024	clinvar