SOS1 E846K

CI-VAR-00000855Explore in graph →CIViC 4107

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
Unmapped disease1unmapped disease
SOS1 E846K	(functional)	Functional	D	Supports Gain Of Function	3	submitted	EID10542 The SOS1 mutation E846K commonly associated with Noonan syndrome was introduced into mouse ES cells using the Cre-Lox recombination system. ES cells expressing mutant SOS1 showed increased levels of p… (full text at CIViC) PMID 21041952 · Chen et al., 2010 · 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.