RABGAP1L
RAB GTPase activating protein 1 like
Summary
Enables GTPase activator activity and small GTPase binding activity. Acts upstream of or within regulation of protein localization. Located in several cellular components, including Golgi apparatus; cilium; and early endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants104 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs76785379 | 1:174,144,062 | C/T | regulatory region variant | — |
| rs10912739 | 1:174,146,656 | A/G | — | — |
| rs79936019 | 1:174,147,475 | G/T | intron variant | — |
| rs185412454 | 1:174,148,044 | G/C | intron variant | — |
| rs12076771 | 1:174,153,284 | T/A | — | — |
| rs1035337401 | 1:174,153,285 | G/A | — | likely pathogenic |
| rs12087441 | 1:174,157,834 | G/A | intron variant | — |
| rs1221602563 | 1:174,188,336 | C/T | — | uncertain significance |
| rs56188862 | 1:174,189,269 | T/C | intron variant | — |
| rs138469250 | 1:174,190,170 | G/A | — | uncertain significance |
| rs17854182 | 1:174,190,205 | A/G | — | benign |
| rs775576293 | 1:174,190,209 | T/G | — | uncertain significance |
| rs768866681 | 1:174,200,369 | A/G | — | uncertain significance |
| rs759981032 | 1:174,200,421 | C/A | — | uncertain significance |
| rs553696340 | 1:174,203,921 | G/A | — | — |
| rs12091012 | 1:174,207,948 | C/G | — | — |
| rs776198500 | 1:174,210,664 | A/G | — | uncertain significance |
| rs143661013 | 1:174,210,668 | A/G | — | uncertain significance |
| rs771611825 | 1:174,210,670 | A/G | — | uncertain significance |
| rs2526567279 | 1:174,210,686 | C/T | — | uncertain significance |
| rs1671831475 | 1:174,210,692 | G/C | — | uncertain significance |
| rs537847739 | 1:174,210,704 | C/T | — | uncertain significance |
| rs371333673 | 1:174,210,790 | G/C | — | uncertain significance |
| rs115073088 | 1:174,215,858 | A/G | intron variant | — |
| rs148341321 | 1:174,219,650 | A/G | — | uncertain significance |
| rs1305762392 | 1:174,219,686 | C/T | — | uncertain significance |
| rs368432186 | 1:174,219,698 | C/A | — | uncertain significance |
| rs143354894 | 1:174,219,725 | G/T | — | uncertain significance |
| rs1672796187 | 1:174,221,671 | A/G | — | uncertain significance |
| rs114017545 | 1:174,222,832 | C/T | intron variant | — |
| rs1384597314 | 1:174,241,586 | G/A | — | uncertain significance |
| rs973214933 | 1:174,245,052 | C/T | — | uncertain significance |
| rs534755457 | 1:174,247,838 | G/T | — | uncertain significance |
| rs1675229409 | 1:174,247,886 | T/C | — | uncertain significance |
| rs114888303 | 1:174,271,559 | G/C | intron variant | — |
| rs142728115 | 1:174,274,146 | A/T | — | uncertain significance |
| rs759306328 | 1:174,274,182 | A/G | — | uncertain significance |
| rs377380635 | 1:174,274,202 | G/C | — | uncertain significance |
| rs770284796 | 1:174,274,235 | A/G | — | uncertain significance |
| rs10912765 | 1:174,291,950 | C/G | intron variant | — |
| rs181516391 | 1:174,297,147 | A/G | intron variant | — |
| rs72713530 | 1:174,306,035 | G/T | — | — |
| rs371119747 | 1:174,324,556 | A/T | — | — |
| rs370164900 | 1:174,340,183 | A/G | — | uncertain significance |
| rs747877567 | 1:174,340,186 | C/T | — | uncertain significance |
| rs778507376 | 1:174,363,272 | C/T | — | uncertain significance |
| rs61826865 | 1:174,371,104 | T/C | — | — |
| rs148499788 | 1:174,371,867 | A/G | intron variant | — |
| rs61826866 | 1:174,376,779 | C/T | intron variant | — |
| rs72713578 | 1:174,399,558 | G/C | intron variant | — |
| rs12092768 | 1:174,432,882 | G/A | intron variant | — |
| rs2901818 | 1:174,455,377 | T/A | — | — |
| rs7522253 | 1:174,466,118 | C/A | — | — |
| rs10912798 | 1:174,480,558 | T/C | intron variant | — |
| rs10912799 | 1:174,480,560 | A/T | intron variant | — |
| rs13375788 | 1:174,493,345 | G/T | — | — |
| rs12062170 | 1:174,497,558 | C/A | — | — |
| rs6425284 | 1:174,499,977 | G/C | — | — |
| rs6681970 | 1:174,501,836 | A/G | intron variant | — |
| rs139464224 | 1:174,501,999 | T/C | intron variant | — |
| rs10798320 | 1:174,509,646 | G/C | — | — |
| rs2142633 | 1:174,515,935 | A/T | — | — |
| rs182221508 | 1:174,527,498 | A/G | intron variant | — |
| rs17301853 | 1:174,552,811 | C/G | — | — |
| rs4651103 | 1:174,565,888 | A/G | intron variant | — |
| rs181658924 | 1:174,566,049 | T/A | intron variant | — |
| rs6657060 | 1:174,589,019 | T/C | intron variant | — |
| rs11487328 | 1:174,601,659 | G/C | intron variant | — |
| rs72715269 | 1:174,606,213 | C/T | intron variant | — |
| rs2527712992 | 1:174,606,544 | A/T | — | uncertain significance |
| rs2527713310 | 1:174,606,571 | A/T | — | uncertain significance |
| rs61747504 | 1:174,606,602 | A/G | — | benign |
| rs56292878 | 1:174,608,128 | T/A | intron variant | — |
| rs138329430 | 1:174,619,318 | G/A | intron variant | — |
| rs898711430 | 1:174,668,702 | A/G | — | uncertain significance |
| rs1215994124 | 1:174,668,770 | G/C | — | uncertain significance |
| rs575263691 | 1:174,683,640 | G/A | — | — |
| rs181010371 | 1:174,707,781 | A/G | intron variant | — |
| rs332801 | 1:174,722,330 | A/G | downstream gene variant | — |
| rs77417259 | 1:174,729,983 | G/T | — | — |
| rs61828068 | 1:174,731,998 | G/A | intron variant | — |
| rs80245686 | 1:174,750,751 | T/A | — | — |
| rs61828088 | 1:174,768,522 | G/A | regulatory region variant | — |
| rs193260452 | 1:174,772,881 | A/G | intron variant | — |
| rs2526086964 | 1:174,781,021 | T/G | — | uncertain significance |
| rs770558370 | 1:174,781,082 | A/G | — | uncertain significance |
| rs199639499 | 1:174,781,083 | G/C | — | uncertain significance |
| rs181467548 | 1:174,810,196 | A/G | intron variant | — |
| rs61828117 | 1:174,822,607 | C/A | — | — |
| rs111830643 | 1:174,828,992 | A/G | intron variant | — |
| rs140588606 | 1:174,835,481 | G/T | — | — |
| rs6425302 | 1:174,851,779 | T/A | intron variant | — |
| rs12078839 | 1:174,861,487 | C/G | upstream gene variant | — |
| rs57512007 | 1:174,870,738 | A/C | downstream gene variant | — |
| rs4651205 | 1:174,872,429 | C/T | intron variant | — |
| rs6691857 | 1:174,885,129 | C/T | intron variant | — |
| rs149820868 | 1:174,886,381 | C/T | regulatory region variant | — |
| rs549669428 | 1:174,895,022 | T/G | — | — |
| rs12061403 | 1:174,924,930 | A/C | upstream gene variant | — |
| rs954694024 | 1:174,926,643 | G/A | — | uncertain significance |
Showing 100 of 104 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.