RRAS2

RAS related 2

Summary

This gene encodes a member of the R-Ras subfamily of Ras-like small GTPases. The encoded protein associates with the plasma membrane and may function as a signal transducer. This protein may play an important role in activating signal transduction pathways that control cell proliferation. Mutations in this gene are associated with the growth of certain tumors. Pseudogenes of this gene are found on chromosomes 1 and 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]

Known Variants68 total

rsidPosition (GRCh37)AllelesClassClinVar
rs857011:14,300,759C/G—benign
rs213393948911:14,300,889A/G—likely benign
rs184945648811:14,300,892G/C—likely benign
rs156495057611:14,300,902C/G—uncertain significance
rs123367113811:14,300,917T/C—uncertain significance
rs37056423311:14,300,927G/A—uncertain significance
rs249409583111:14,300,938G/C—uncertain significance
rs1102317411:14,300,946A/G—likely benign
rs249409594911:14,300,972T/G—uncertain significance
rs78279302411:14,300,988C/A—likely benign
rs78272621111:14,303,158G/A—uncertain significance
rs78231183711:14,303,191T/C—uncertain significance
rs18976081211:14,303,222T/C—likely benign
rs78209287111:14,303,226T/G—uncertain significance
rs37732124511:14,303,235C/T—uncertain significance
rs78204728611:14,303,236G/A—uncertain significance
rs54996625811:14,303,263T/A—benign
rs230397211:14,303,282T/A—benign
rs3423844511:14,315,915C/T—benign
rs184749470311:14,316,023T/C—likely benign
rs155494628311:14,316,061T/A—uncertain significance
rs56670322511:14,316,075C/T—uncertain significance
rs78249057111:14,316,076G/C—uncertain significance
rs249413789511:14,316,095C/G—uncertain significance
rs249413792811:14,316,107C/G—uncertain significance
rs57123455511:14,316,111T/C—uncertain significance
rs78229549411:14,316,129A/C—likely benign
rs8024738811:14,316,287A/G—benign
rs249413877011:14,316,294T/G—likely benign
rs249413887511:14,316,318G/A—uncertain significance
rs155494632911:14,316,334A/T—uncertain significance
rs78249207411:14,316,347G/A—likely benign
rs213396195611:14,316,358T/A—uncertain significance
rs155494634411:14,316,373T/A—uncertain significance
rs11395499711:14,316,390T/Amissense variantpathogenic
rs116001768011:14,316,393C/T—likely pathogenic
rs78180668011:14,316,395T/C—likely benign
rs78245790811:14,316,397C/T—likely pathogenic
rs36817766811:14,317,305T/C—uncertain significance
rs249414183311:14,317,314T/C—uncertain significance
rs184752967111:14,317,315A/G—uncertain significance
rs78259726611:14,317,322C/T—uncertain significance
rs78224519511:14,317,372G/A—likely benign
rs213396344611:14,317,375T/C—likely benign
rs184753134811:14,317,377G/C—uncertain significance
rs155494651411:14,317,387C/T—likely benign
rs78267086911:14,317,388G/A—uncertain significance
rs11720636911:14,335,876T/Cregulatory region variant—
rs6188396311:14,338,703G/Aintron variant—
rs5591324911:14,344,775T/Gregulatory region variant—
rs11750284011:14,357,920A/Gintron variant—
rs297033211:14,360,435G/T——
rs1227037411:14,375,079T/Cintron variant—
rs19085049211:14,375,137T/Cintron variant—
rs249394967211:14,379,800T/C—uncertain significance
rs155495584211:14,380,318C/A—uncertain significance
rs155495584311:14,380,319T/C—uncertain significance
rs18487210111:14,380,327G/A—likely benign
rs249395181311:14,380,346C/T—pathogenic
rs159149577911:14,380,349C/A—pathogenic
rs213404872611:14,380,350C/A—pathogenic
rs155495585111:14,380,358A/G—uncertain significance
rs249395198911:14,380,385C/T—uncertain significance
rs1083224611:14,380,828G/A—benign
rs1102319711:14,380,998G/Aregulatory region variant—
rs56215599311:14,385,938A/G—uncertain significance
rs7503307911:14,385,941A/G—benign
rs451747511:14,386,145A/G—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.