VHL Null (point mutation codon 238)

CI-VAR-00003016Explore in graph →CIViC 3262

Curated evidence

Evidence by cancer (1 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.

civicCuratedShowing 1–1 of 1 evidence items across 1 cancer context on this page · levels, directions and significance as curated at the source; each row links to its CIViC record.

Molecular profile	Therapy	Type	Level	Direction · significance	Rating (1–5)	Status	Evidence	Source
Von Hippel-Lindau Disease1unmapped disease
VHL Null (point mutation codon 238)	(predisposing)	Predisposing	C	N/A N/A	2	submitted	EID9050 17 patients with VHL disease followed by the Department of Endocrinology at St Bartholomew’s Hospital since 1988 were retrospectively reviewed. Patient 1 (32Y old male) and 2 (29Y olf female) belonged… (full text at CIViC) PMID 12390333 · Mukhopadhyay et al., 2002 · Open in CIViC	civic

ClinVar

Clinical significance (0)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

Data not yet available

No ClinVar interpretation attached to this variant.