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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8608198
Species: Homo sapiens
RGD Object: Variant
Symbol: CV49152
Name: NM_005633.4(SOS1):c.1655G>C (p.Arg552Thr)
Acc ID: DOID:0080690
Term: RASopathy
Definition: A syndrome that has_material_basis_in mutations in genes that alter the Ras subfamily and mitogen-activated protein kinases that control signal transduction. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/RASopathy "DO" "DO", https://www.nature.com/articles/jhg2015114 "DO" "DO", https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115674/ "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
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