VHL S65T (c.193T>A)

CI-VAR-00004099Explore in graph →NP_000542.1:p.Ser65ThrNM_000551.3:c.193T>ACIViC 3048

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 S65T (c.193T>A)	(predisposing)	Predisposing	C	N/A N/A	2	submitted	EID8253 A series of 28 pheochromacytomas from 28 patients from the Freiburg International Pheochromaccytoma Registry were used to study for somatic point mutation variants and loss of heterozygosity. 9 out of… (full text at CIViC) PMID 22573489 · Weber et al., 2012 · 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.