GRTP1

growth hormone regulated TBC protein 1

Summary

Predicted to enable GTPase activator activity. Predicted to be active in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants48 total

rsidPosition (GRCh37)AllelesClassClinVar
rs20101133313:113,978,823G/A—uncertain significance
rs77777782713:113,978,846T/C—likely benign
rs37537361013:113,978,849G/A—uncertain significance
rs124174692213:113,979,983A/G—uncertain significance
rs14674121913:113,979,986G/A—uncertain significance
rs250437660313:113,980,019A/G—uncertain significance
rs140358863513:113,980,033A/C—likely benign
rs76428658113:113,980,082T/G—uncertain significance
rs77874371713:113,980,125C/A—uncertain significance
rs140732046513:113,980,253A/G—uncertain significance
rs13889086413:113,980,274C/T—uncertain significance
rs143360981813:113,980,283A/T—uncertain significance
rs37085216213:113,980,302C/T—uncertain significance
rs37364751313:113,980,307C/T—uncertain significance
rs250437827513:113,980,329C/G—uncertain significance
rs14734727213:113,980,340G/A—uncertain significance
rs14801619913:113,980,343C/T—uncertain significance
rs77118533913:113,980,356C/G—uncertain significance
rs181066813:113,998,780G/T——
rs6196659013:114,000,418C/A—likely benign
rs120829750213:114,000,491G/A—likely benign
rs126576421013:114,000,556G/C—likely benign
rs142438365113:114,000,616C/T—likely benign
rs86799746313:114,000,817G/A—likely benign
rs131641741213:114,000,833C/A—likely benign
rs141991229613:114,000,841A/G—likely benign
rs142772624013:114,000,863C/A—likely benign
rs138183469113:114,000,914C/T—likely benign
rs37139860413:114,000,954T/A—likely benign
rs138289328813:114,000,984T/A—likely benign
rs119341284613:114,000,989G/A—likely benign
rs14776238413:114,002,291G/C—benign
rs7907916313:114,003,459T/Cupstream gene variant—
rs204325359113:114,005,213T/C—uncertain significance
rs75774936713:114,005,214T/C—uncertain significance
rs136896350913:114,005,243G/A—uncertain significance
rs14627753113:114,005,253G/A—uncertain significance
rs1243081913:114,006,516A/Cintron variant—
rs138874864113:114,009,653C/T—uncertain significance
rs75433471613:114,009,672C/G—likely benign
rs19998686313:114,009,701C/T—uncertain significance
rs731703813:114,012,898C/Tdownstream gene variant—
rs1087447213:114,016,802A/Tdownstream gene variant—
rs490762213:114,016,886G/T——
rs954975313:114,018,038C/G——
rs121647529313:114,018,098C/G—uncertain significance
rs57322249413:114,018,136C/A—uncertain significance
rs20014449713:114,018,184T/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.