VHL NM_000551.4(VHL):c.379_380insCAG (p.Asp126_Gly127insAla) — variant · CancerIndex

Variant · Insertion

VHL NM_000551.4(VHL):c.379_380insCAG (p.Asp126_Gly127insAla)

CI-VAR-00103850Explore in graph →p.Asp126_Gly127insAlaNM_000551.4:c.379_380insCAGClinVar 578561 rs1559428103

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
578561	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Chuvash polycythemia; Von Hippel-Lindau syndrome; Hereditary cancer-predisposing syndrome	germline	2	Dec 05, 2024	clinvar