Clinical Domain Working Groups
RASopathy Variant Curation Expert Panel
Membership DocumentsThe ClinGen RASopathy Expert Panel aims to provide high quality, standardized curation of RASopathy gene variants.
Using the recently released ACMG standards and guidelines for the interpretations of sequence variants as our foundation, we refined classification criteria to specifically apply to BRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1, RIT1, SHOC2, SOS1, and SOS2 relative to their pathogenicity and mechanism, and considering their allele frequency compared to the incidence of these Noonan syndrome spectrum disorders.
The RASopathy Expert Panel aims to systematically aid in resolution of variant classification differences in ClinVar and provide further curation of the genes involved in the RASopathies.
Expert Panel Status
Documents
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ClinGen RASopathy Variant Curation Expert Panel COIConflict Of Interest (COI) - August 25, 2022
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ClinGen's RASopathy Expert Panel consensus methods for variant interpretationPublications - March 1, 2018
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ClinGen RASopathy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1Curation Activity Procedures - July 18, 2017 Archived Document
Expert Panel Membership
Membership spans many fields, including genetics, medical, academia, and industry.