ARHGAP15
Rho GTPase activating protein 15
Summary
RHO GTPases (see ARHA; MIM 165390) regulate diverse biologic processes, and their activity is regulated by RHO GTPase-activating proteins (GAPs), such as ARHGAP15 (Seoh et al., 2003 [PubMed 12650940]).[supplied by OMIM, Mar 2008]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs354707 | 2:143,886,437 | T/A | regulatory region variant | — |
| rs144449054 | 2:143,889,934 | G/A | regulatory region variant | — |
| rs150127285 | 2:143,913,111 | C/T | — | uncertain significance |
| rs373692174 | 2:143,913,222 | C/A | — | uncertain significance |
| rs563447271 | 2:143,914,774 | T/C | — | — |
| rs35713119 | 2:143,948,355 | A/G | — | — |
| rs35028264 | 2:143,972,880 | G/T | intron variant | — |
| rs757406465 | 2:143,974,001 | G/A | — | uncertain significance |
| rs1030218974 | 2:143,986,163 | A/G | — | uncertain significance |
| rs2468403381 | 2:144,008,170 | G/A | — | uncertain significance |
| rs2381401 | 2:144,020,974 | C/T | regulatory region variant | — |
| rs2381459 | 2:144,056,371 | A/G | intron variant | — |
| rs10460253 | 2:144,085,491 | C/A | — | — |
| rs10176394 | 2:144,096,374 | T/C | intron variant | — |
| rs13008966 | 2:144,117,605 | A/C | intron variant | — |
| rs10496949 | 2:144,153,344 | G/T | — | — |
| rs62172064 | 2:144,154,888 | T/C | intron variant | — |
| rs34210137 | 2:144,154,917 | A/T | — | — |
| rs1320139 | 2:144,158,177 | C/G | intron variant | — |
| rs140397066 | 2:144,162,105 | A/G | intron variant | — |
| rs4662330 | 2:144,186,475 | T/C | regulatory region variant | — |
| rs199653389 | 2:144,193,166 | G/T | — | likely benign |
| rs766488154 | 2:144,193,192 | A/G | — | uncertain significance |
| rs2467506710 | 2:144,193,194 | T/C | — | uncertain significance |
| rs368334646 | 2:144,193,229 | G/C | — | uncertain significance |
| rs2467512236 | 2:144,194,508 | A/T | — | uncertain significance |
| rs375998378 | 2:144,194,545 | A/G | — | uncertain significance |
| rs12691680 | 2:144,204,338 | C/G | — | — |
| rs35942385 | 2:144,208,523 | G/T | intron variant | — |
| rs13411140 | 2:144,215,811 | C/T | intron variant | — |
| rs13024996 | 2:144,225,215 | C/A | intron variant | — |
| rs4273169 | 2:144,231,309 | G/T | — | — |
| rs28380327 | 2:144,232,491 | A/T | intron variant | — |
| rs191784266 | 2:144,234,080 | C/T | regulatory region variant | — |
| rs751971221 | 2:144,244,987 | G/A | — | uncertain significance |
| rs868812296 | 2:144,244,990 | T/C | — | uncertain significance |
| rs778935227 | 2:144,245,020 | G/A | — | uncertain significance |
| rs35789697 | 2:144,248,718 | G/A | intron variant | — |
| rs13428598 | 2:144,250,487 | C/T | intron variant | — |
| rs10191758 | 2:144,263,280 | A/G | regulatory region variant | — |
| rs4561605 | 2:144,272,150 | C/G | regulatory region variant | — |
| rs1693959539 | 2:144,276,864 | G/A | — | uncertain significance |
| rs765197653 | 2:144,276,874 | G/A | — | uncertain significance |
| rs6736741 | 2:144,278,534 | C/T | intron variant | — |
| rs4278879 | 2:144,299,242 | T/A | — | — |
| rs6733817 | 2:144,300,147 | A/G | intron variant | — |
| rs10084164 | 2:144,302,613 | G/C | — | — |
| rs6731747 | 2:144,308,396 | T/A | intron variant | — |
| rs6717024 | 2:144,308,780 | C/G | intron variant | — |
| rs2467941479 | 2:144,314,043 | T/C | — | uncertain significance |
| rs10170378 | 2:144,334,078 | C/G | — | — |
| rs11894956 | 2:144,336,132 | T/A | intron variant | — |
| rs4662208 | 2:144,338,448 | A/C | intron variant | — |
| rs4662344 | 2:144,348,858 | T/A | — | — |
| rs1490866906 | 2:144,381,746 | G/A | — | uncertain significance |
| rs71350022 | 2:144,395,796 | G/A | — | — |
| rs10928195 | 2:144,428,608 | C/A | — | — |
| rs770105549 | 2:144,461,008 | A/G | — | uncertain significance |
| rs201019600 | 2:144,461,048 | C/T | — | uncertain significance |
| rs776074764 | 2:144,461,057 | G/A | — | uncertain significance |
| rs764811617 | 2:144,461,074 | C/T | — | uncertain significance |
| rs73961845 | 2:144,478,983 | A/G | intron variant | — |
| rs760147596 | 2:144,525,593 | C/T | — | uncertain significance |
| rs781102282 | 2:144,525,632 | G/A | — | uncertain significance |
| rs369327090 | 2:144,525,667 | A/G | — | uncertain significance |
| rs2467486763 | 2:144,525,677 | A/G | — | uncertain significance |
| rs1473524669 | 2:144,525,685 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.