RALGAPB

Ral GTPase activating protein non-catalytic subunit beta

Summary

Enables protein heterodimerization activity. Predicted to be involved in Ral protein signal transduction and activation of GTPase activity. Predicted to act upstream of or within regulation of exocyst localization and regulation of protein localization. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants71 total

rsidPosition (GRCh37)AllelesClassClinVar
rs156890309220:37,117,112C/G—uncertain significance
rs139629886220:37,121,637A/G—uncertain significance
rs53744770820:37,125,379T/G——
rs75655578220:37,126,063C/T—uncertain significance
rs37159366020:37,126,064G/A—uncertain significance
rs74657654220:37,126,085G/A—uncertain significance
rs77106412020:37,126,150A/G—uncertain significance
rs1698735020:37,128,080T/C—benign
rs146521957220:37,128,159C/G—uncertain significance
rs14771860820:37,128,264C/G—uncertain significance
rs14157565420:37,133,461T/Cregulatory region variant—
rs127377938120:37,137,727C/T—uncertain significance
rs208585814120:37,137,790C/G—uncertain significance
rs20205938720:37,137,805A/C—benign
rs102345610420:37,137,844A/G—uncertain significance
rs208616643220:37,146,190G/A—uncertain significance
rs122756244120:37,146,248G/A—uncertain significance
rs208617005420:37,146,277G/A—uncertain significance
rs208617598920:37,146,439C/T—uncertain significance
rs122542679520:37,146,484T/C—uncertain significance
rs4127694620:37,146,510A/G—benign
rs74737708020:37,146,532C/G—uncertain significance
rs75234377120:37,146,600C/A—uncertain significance
rs77608175120:37,150,193A/G—uncertain significance
rs75095271820:37,153,462A/G—uncertain significance
rs19957581720:37,153,556T/A—uncertain significance
rs208643095320:37,154,091G/A—uncertain significance
rs54676303620:37,154,553A/G—no classification for the single variant
rs208664172520:37,159,846T/C—uncertain significance
rs4128283020:37,161,446C/T—benign
rs75802211620:37,163,795G/T—likely pathogenic
rs251650938320:37,163,798A/G—uncertain significance
rs77716911520:37,168,447G/A—uncertain significance
rs607052120:37,168,469T/G—benign
rs18955972220:37,169,748A/G—likely benign
rs76607561320:37,174,903G/A—uncertain significance
rs251656883520:37,174,911C/T—likely benign
rs251656931620:37,174,959A/G—uncertain significance
rs214541508020:37,175,041C/T—uncertain significance
rs251658253920:37,177,394C/G—uncertain significance
rs80554820:37,177,423A/G—benign
rs37593808720:37,179,768T/G—uncertain significance
rs14117956120:37,179,783C/G—uncertain significance
rs37466186320:37,182,546G/A—uncertain significance
rs251661240720:37,182,715T/G—uncertain significance
rs75699096020:37,186,938G/A—uncertain significance
rs76533354420:37,186,953C/T—uncertain significance
rs19954364020:37,187,004G/T—uncertain significance
rs214547318420:37,187,017A/G—uncertain significance
rs19039442220:37,187,093A/C—uncertain significance
rs37035774020:37,191,188T/C—uncertain significance
rs7659185520:37,191,214C/T—benign
rs251666485920:37,194,002A/T—uncertain significance
rs78055615220:37,194,010T/C—uncertain significance
rs78138433220:37,195,756A/G—uncertain significance
rs11758108920:37,195,773T/C—benign
rs75006879120:37,195,786A/G—uncertain significance
rs120972339920:37,195,799C/T—uncertain significance
rs251667343420:37,195,841C/G—uncertain significance
rs13866885620:37,198,538C/T—benign
rs14267829320:37,198,582C/T—benign
rs14738401020:37,198,625G/A—uncertain significance
rs13954310320:37,199,443G/A—benign
rs148275663320:37,199,448G/C—uncertain significance
rs251668893220:37,199,491G/A—pathogenic
rs208835012720:37,202,899A/C—uncertain significance
rs86735413520:37,202,905C/T—uncertain significance
rs208835162820:37,202,933G/C—uncertain significance
rs251670460620:37,202,936C/T—uncertain significance
rs13888652220:37,203,484T/C—benign
rs136537214220:37,203,606C/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.