ARAP3
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3
Summary
This gene encodes a phosphoinositide binding protein containing ARF-GAP, RHO-GAP, RAS-associating, and pleckstrin homology domains. The ARF-GAP and RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton and cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Sep 2015]
Known Variants111 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1013538934 | 5:141,033,594 | G/T | — | uncertain significance |
| rs370453653 | 5:141,033,720 | G/A | — | uncertain significance |
| rs145931062 | 5:141,033,728 | G/A | — | uncertain significance |
| rs548344777 | 5:141,033,785 | A/T | — | uncertain significance |
| rs375260150 | 5:141,033,869 | G/A | — | uncertain significance |
| rs2531785160 | 5:141,033,999 | T/C | — | uncertain significance |
| rs141682206 | 5:141,034,952 | G/A | — | uncertain significance |
| rs143698821 | 5:141,034,963 | C/T | — | likely benign |
| rs758768178 | 5:141,035,225 | T/C | — | uncertain significance |
| rs369505822 | 5:141,035,235 | G/A | — | uncertain significance |
| rs148377698 | 5:141,035,480 | C/T | — | uncertain significance |
| rs2531808334 | 5:141,035,807 | C/A | — | uncertain significance |
| rs376948840 | 5:141,035,809 | C/T | — | uncertain significance |
| rs539283748 | 5:141,035,828 | G/A | — | uncertain significance |
| rs140628013 | 5:141,036,168 | C/T | — | uncertain significance |
| rs754569933 | 5:141,036,195 | C/T | — | uncertain significance |
| rs144504101 | 5:141,036,304 | T/A | — | uncertain significance |
| rs757031961 | 5:141,036,315 | G/T | — | uncertain significance |
| rs372104720 | 5:141,038,004 | G/T | — | uncertain significance |
| rs199947032 | 5:141,038,037 | T/C | — | uncertain significance |
| rs749857920 | 5:141,038,162 | T/C | — | uncertain significance |
| rs200505511 | 5:141,038,184 | T/C | — | uncertain significance |
| rs141018946 | 5:141,038,879 | A/G | intron variant | — |
| rs201916487 | 5:141,039,040 | C/T | — | uncertain significance |
| rs1455899942 | 5:141,039,396 | C/T | — | uncertain significance |
| rs145892711 | 5:141,039,402 | C/T | — | uncertain significance |
| rs567097746 | 5:141,039,426 | C/T | — | uncertain significance |
| rs368544318 | 5:141,039,479 | G/A | — | uncertain significance |
| rs375379752 | 5:141,041,284 | C/T | — | uncertain significance |
| rs137994820 | 5:141,041,290 | T/C | — | uncertain significance |
| rs774760084 | 5:141,041,310 | A/C | — | uncertain significance |
| rs762292586 | 5:141,041,627 | C/T | — | uncertain significance |
| rs766997460 | 5:141,041,656 | G/C | — | uncertain significance |
| rs866209168 | 5:141,041,670 | G/A | — | uncertain significance |
| rs780063109 | 5:141,041,681 | T/C | — | uncertain significance |
| rs750214735 | 5:141,041,748 | G/A | — | uncertain significance |
| rs1054559355 | 5:141,041,778 | G/A | — | uncertain significance |
| rs145752053 | 5:141,041,817 | G/A | — | uncertain significance |
| rs767197668 | 5:141,044,517 | A/T | — | uncertain significance |
| rs779396832 | 5:141,044,573 | C/T | — | uncertain significance |
| rs541018224 | 5:141,044,600 | C/T | — | uncertain significance |
| rs554504713 | 5:141,044,603 | C/T | — | likely benign |
| rs149211277 | 5:141,044,626 | C/T | — | uncertain significance |
| rs775409811 | 5:141,044,881 | C/T | — | uncertain significance |
| rs756918238 | 5:141,046,005 | C/T | — | uncertain significance |
| rs200762467 | 5:141,046,008 | C/T | — | uncertain significance |
| rs143455055 | 5:141,046,035 | G/C | — | uncertain significance |
| rs369718019 | 5:141,046,039 | G/T | — | uncertain significance |
| rs147978083 | 5:141,046,045 | G/A | — | uncertain significance |
| rs762582404 | 5:141,046,080 | C/T | — | uncertain significance |
| rs141698932 | 5:141,046,087 | G/T | — | uncertain significance |
| rs1228616758 | 5:141,046,116 | G/T | — | uncertain significance |
| rs1004812678 | 5:141,046,161 | C/T | — | uncertain significance |
| rs539893395 | 5:141,046,171 | C/T | — | uncertain significance |
| rs568939612 | 5:141,049,300 | C/A | — | uncertain significance |
| rs1596487323 | 5:141,049,313 | G/A | — | uncertain significance |
| rs377450993 | 5:141,049,346 | C/G | — | uncertain significance |
| rs758544678 | 5:141,049,350 | C/T | — | likely benign |
| rs374645011 | 5:141,049,576 | T/A | — | uncertain significance |
| rs1264379093 | 5:141,049,622 | G/A | — | uncertain significance |
| rs775720602 | 5:141,050,085 | G/A | — | uncertain significance |
| rs1230022777 | 5:141,050,100 | G/C | — | uncertain significance |
| rs374649374 | 5:141,050,159 | C/T | — | uncertain significance |
| rs2531970099 | 5:141,050,846 | C/A | — | uncertain significance |
| rs200759771 | 5:141,050,892 | C/T | — | uncertain significance |
| rs2099911415 | 5:141,050,895 | C/G | — | uncertain significance |
| rs2531972404 | 5:141,050,951 | A/G | — | uncertain significance |
| rs149532200 | 5:141,051,195 | C/T | — | uncertain significance |
| rs144248427 | 5:141,051,196 | G/A | — | uncertain significance |
| rs373493885 | 5:141,051,204 | C/T | — | uncertain significance |
| rs142370797 | 5:141,051,274 | C/T | — | uncertain significance |
| rs188329291 | 5:141,051,286 | G/A | — | uncertain significance |
| rs924469231 | 5:141,051,295 | G/A | — | uncertain significance |
| rs2531983783 | 5:141,051,677 | T/C | — | uncertain significance |
| rs781686907 | 5:141,051,722 | C/T | — | uncertain significance |
| rs141117484 | 5:141,051,758 | C/T | — | uncertain significance |
| rs756090076 | 5:141,052,171 | G/A | — | uncertain significance |
| rs746071456 | 5:141,052,183 | C/T | — | uncertain significance |
| rs1306988881 | 5:141,052,417 | G/T | — | uncertain significance |
| rs765300785 | 5:141,052,429 | T/G | — | uncertain significance |
| rs138728743 | 5:141,052,474 | C/T | — | uncertain significance |
| rs774581128 | 5:141,052,480 | A/T | — | uncertain significance |
| rs2531998285 | 5:141,052,597 | A/C | — | uncertain significance |
| rs148182244 | 5:141,052,651 | C/T | — | uncertain significance |
| rs200157148 | 5:141,052,664 | T/C | — | uncertain significance |
| rs756784339 | 5:141,052,987 | A/G | — | uncertain significance |
| rs115551494 | 5:141,053,220 | C/T | — | uncertain significance |
| rs149350776 | 5:141,053,229 | G/A | — | uncertain significance |
| rs139633951 | 5:141,053,268 | C/G | — | uncertain significance |
| rs144278581 | 5:141,053,295 | G/A | — | likely benign |
| rs2099911764 | 5:141,053,316 | G/C | — | uncertain significance |
| rs771211262 | 5:141,053,349 | C/T | — | uncertain significance |
| rs777082590 | 5:141,059,163 | G/T | — | uncertain significance |
| rs767139655 | 5:141,059,193 | T/C | — | uncertain significance |
| rs372228658 | 5:141,059,223 | A/C | — | uncertain significance |
| rs201759718 | 5:141,059,678 | A/T | — | uncertain significance |
| rs764484654 | 5:141,059,767 | G/A | — | uncertain significance |
| rs138194565 | 5:141,059,785 | T/G | — | uncertain significance |
| rs757656810 | 5:141,059,788 | G/A | — | uncertain significance |
| rs142901719 | 5:141,059,794 | G/A | — | uncertain significance |
Showing 100 of 111 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.