SRPX2 NM_014467.3(SRPX2):c.981C>G (p.Asn327Lys)

CI-VAR-00031891Explore in graph →p.Asn327LysNM_014467.3:c.981C>GClinVar 199131 rs370033099

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
199131	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked; Familial cancer of breast	germline	5	Feb 04, 2022	clinvar