VHL R82P (c.245G>C)

CI-VAR-00003907Explore in graph →NP_000542.1:p.Arg82ProNM_000551.3:c.245G>CClinVar 193118 CIViC 1980 rs794726890

Curated evidence

Evidence by cancer (10 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 1–10 of 10 evidence items across 2 cancer contexts 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
Kidney Carcinoma1
VHL R82P (c.245G>C)	(predisposing)	Predisposing	C	Supports Uncertain Significance	3	submitted	EID6892 Tumors from 110 patients with sporadic renal carcinoma were analyzed for VHL mutations and loss of heterozygosity. 56 of the 98 samples from sporadic, clear cell renal carcinoma patients were identifi… (full text at CIViC) PMID 7915601 · Gnarra et al., 1994 · Open in CIViC	civic
Von Hippel-Lindau Disease9unmapped disease
VHL R82P (c.245G>C)	(predisposing)	Predisposing	C	Supports Predisposition	4	submitted	EID5320 A Mexican family with Von Hippel-Lindau disease was identified. The family consisted of 6 clinically affected members, 3 of which received genetic testing that demonstrated the presence of the above m… (full text at CIViC) PMID ·

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
193118	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Von Hippel-Lindau syndrome	germline	3	Feb 14, 2019	clinvar