SOS2

SOS Ras/Rho guanine nucleotide exchange factor 2

Summary

This gene encodes a regulatory protein that is involved in the positive regulation of ras proteins. Mutations in this gene are associated with Noonan Syndrome-9. [provided by RefSeq, Jul 2016]

Known Variants1,285 total

rsidPosition (GRCh37)AllelesClassClinVar
rs213946152014:50,584,828C/T—uncertain significance
rs7471409014:50,585,012A/T—likely benign
rs14266680314:50,585,064A/G—uncertain significance
rs93885851414:50,585,065T/C—likely benign
rs14652723914:50,585,074T/G—conflicting classifications of pathogenicity
rs77626660214:50,585,077T/C—likely benign
rs52757640414:50,585,080A/G—likely benign
rs76481918114:50,585,086T/C—likely benign
rs88604192914:50,585,093G/A—uncertain significance
rs250275347714:50,585,096A/G—uncertain significance
rs76605765814:50,585,101G/A—likely benign
rs95032203414:50,585,103A/G—uncertain significance
rs213946274814:50,585,104C/A—uncertain significance
rs75140806314:50,585,107T/C—likely benign
rs143333940814:50,585,108G/T—uncertain significance
rs14099572814:50,585,109G/T—uncertain significance
rs74951369714:50,585,110G/C—likely benign
rs14342706414:50,585,116C/T—likely benign
rs86592233014:50,585,117G/A—conflicting classifications of pathogenicity
rs74631729414:50,585,122C/G—conflicting classifications of pathogenicity
rs77267387314:50,585,126C/T—conflicting classifications of pathogenicity
rs77597383114:50,585,127G/T—likely benign
rs121478159514:50,585,131G/C—uncertain significance
rs250275407114:50,585,133A/G—uncertain significance
rs75912432414:50,585,159T/C—conflicting classifications of pathogenicity
rs18473933614:50,585,160G/A—conflicting classifications of pathogenicity
rs134092562514:50,585,163G/A—uncertain significance
rs250275441114:50,585,178T/G—likely benign
rs124488186814:50,585,192G/T—uncertain significance
rs76158097214:50,585,193G/C—conflicting classifications of pathogenicity
rs90098625414:50,585,199G/A—uncertain significance
rs250275468314:50,585,200A/G—likely benign
rs188338172314:50,585,211G/C—uncertain significance
rs141798452114:50,585,212A/G—likely benign
rs37615821814:50,585,216T/C—uncertain significance
rs250275502714:50,585,219T/C—uncertain significance
rs250275509214:50,585,223T/G—uncertain significance
rs116550163714:50,585,224A/G—likely benign
rs250275516214:50,585,229T/C—uncertain significance
rs14680299414:50,585,231A/G—likely benign
rs116319920914:50,585,236A/G—likely benign
rs37161997114:50,585,237T/C—likely benign
rs5836546514:50,585,243C/T—conflicting classifications of pathogenicity
rs250275542414:50,585,244G/A—uncertain significance
rs20010474514:50,585,246C/T—conflicting classifications of pathogenicity
rs100549841714:50,585,247G/T—uncertain significance
rs222727614:50,585,248C/G—likely benign
rs128626010214:50,585,249G/A—conflicting classifications of pathogenicity
rs250275563614:50,585,251T/C—likely benign
rs75752834414:50,585,253C/T—uncertain significance
rs250275577914:50,585,256T/C—uncertain significance
rs250275583414:50,585,261G/A—uncertain significance
rs127134117314:50,585,263G/C—likely benign
rs213946402114:50,585,264G/A—uncertain significance
rs213946405014:50,585,267G/A—uncertain significance
rs105311879714:50,585,268T/C—likely benign
rs56934310514:50,585,273G/C—conflicting classifications of pathogenicity
rs213946411114:50,585,276G/A—uncertain significance
rs250275614914:50,585,277G/A—uncertain significance
rs78077201814:50,585,279G/C—conflicting classifications of pathogenicity
rs155536763714:50,585,280T/G—uncertain significance
rs116304801914:50,585,282C/T—likely benign
rs74752158914:50,585,287C/T—likely benign
rs76909350514:50,585,288G/A—conflicting classifications of pathogenicity
rs134439675914:50,585,289A/C—conflicting classifications of pathogenicity
rs15039335814:50,585,292T/C—likely benign
rs74772685614:50,585,294G/T—uncertain significance
rs76953608714:50,585,299C/T—likely benign
rs77258701614:50,585,300G/C—uncertain significance
rs76259345114:50,585,303C/G—conflicting classifications of pathogenicity
rs250275664514:50,585,305A/C—uncertain significance
rs122171976714:50,585,314G/A—likely benign
rs13813301014:50,585,317C/A—likely benign
rs188339301614:50,585,320G/C—uncertain significance
rs76725740514:50,585,323T/G—likely benign
rs75252540014:50,585,326A/C—conflicting classifications of pathogenicity
rs76191778314:50,585,332G/A—likely benign
rs147124534014:50,585,339T/C—conflicting classifications of pathogenicity
rs250275705314:50,585,340G/A—uncertain significance
rs250275708314:50,585,342C/G—uncertain significance
rs140691486414:50,585,347T/A—likely benign
rs250275724514:50,585,353T/C—likely benign
rs140379633914:50,585,354G/A—uncertain significance
rs250275727714:50,585,355G/A—uncertain significance
rs250275733514:50,585,361G/C—uncertain significance
rs20175616814:50,585,363T/G—conflicting classifications of pathogenicity
rs250275757514:50,585,377T/A—likely benign
rs78167465314:50,585,379T/C—likely benign
rs74860727414:50,585,380A/T—uncertain significance
rs250275763314:50,585,382A/C—uncertain significance
rs250275764714:50,585,383G/C—uncertain significance
rs101859296414:50,585,384T/C—uncertain significance
rs76932981714:50,585,388C/G—conflicting classifications of pathogenicity
rs14932198314:50,585,389T/G—likely benign
rs188339635314:50,585,390G/A—uncertain significance
rs120258236314:50,585,396C/T—conflicting classifications of pathogenicity
rs123248920114:50,585,397G/A—conflicting classifications of pathogenicity
rs250275782314:50,585,398A/C—likely benign
rs250275791114:50,585,404A/C—likely benign
rs250275792014:50,585,406C/T—uncertain significance

Showing 100 of 1,285 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.