DAB2IP
DAB2 interacting protein
Summary
DAB2IP is a Ras (MIM 190020) GTPase-activating protein (GAP) that acts as a tumor suppressor. The DAB2IP gene is inactivated by methylation in prostate and breast cancers (Yano et al., 2005 [PubMed 15386433]).[supplied by OMIM, May 2010]
Known Variants98 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7042542 | 9:124,328,048 | T/G | upstream gene variant | — |
| rs10985332 | 9:124,372,152 | C/T | regulatory region variant | — |
| rs2243421 | 9:124,393,324 | C/T | intron variant | — |
| rs555996 | 9:124,396,311 | C/G | intron variant | — |
| rs10818579 | 9:124,414,905 | G/T | — | — |
| rs10985344 | 9:124,416,940 | G/A | regulatory region variant | — |
| rs10985348 | 9:124,419,722 | G/A | — | — |
| rs7025486 | 9:124,422,403 | A/G | intron variant | — |
| rs80293317 | 9:124,426,333 | T/G | — | — |
| rs1571801 | 9:124,427,373 | G/A | — | — |
| rs562494615 | 9:124,434,630 | C/G | — | — |
| rs377424901 | 9:124,440,984 | G/A | — | uncertain significance |
| rs2490780185 | 9:124,441,024 | C/A | — | uncertain significance |
| rs373956059 | 9:124,441,036 | G/C | — | likely benign |
| rs368660589 | 9:124,441,059 | C/T | — | uncertain significance |
| rs747666068 | 9:124,461,604 | G/A | — | uncertain significance |
| rs200769141 | 9:124,461,666 | C/T | — | likely benign |
| rs1363376652 | 9:124,461,716 | C/T | — | uncertain significance |
| rs35061590 | 9:124,476,013 | G/T | intron variant | — |
| rs13290547 | 9:124,487,495 | C/T | regulatory region variant | — |
| rs145251128 | 9:124,499,980 | G/A | — | likely benign |
| rs531428398 | 9:124,517,166 | C/G | — | — |
| rs200818458 | 9:124,519,307 | G/A | — | likely benign |
| rs1345798296 | 9:124,519,332 | G/A | — | uncertain significance |
| rs556227873 | 9:124,519,356 | G/T | — | uncertain significance |
| rs576059169 | 9:124,519,357 | C/T | — | uncertain significance |
| rs2491017732 | 9:124,519,432 | A/G | — | uncertain significance |
| rs1032410166 | 9:124,521,177 | G/A | — | uncertain significance |
| rs1349220521 | 9:124,521,184 | C/T | — | uncertain significance |
| rs1202760174 | 9:124,521,229 | G/A | — | uncertain significance |
| rs114266755 | 9:124,521,255 | C/A | — | benign |
| rs3747851 | 9:124,521,260 | G/A | synonymous variant | — |
| rs758625862 | 9:124,521,268 | C/T | — | uncertain significance |
| rs1463043286 | 9:124,522,279 | G/A | — | uncertain significance |
| rs2491027051 | 9:124,522,282 | C/G | — | uncertain significance |
| rs767688313 | 9:124,522,354 | G/A | — | uncertain significance |
| rs1428145625 | 9:124,522,377 | C/T | — | uncertain significance |
| rs34839326 | 9:124,522,400 | G/A | — | benign |
| rs764203323 | 9:124,522,467 | G/A | — | uncertain significance |
| rs1321520385 | 9:124,522,474 | A/G | — | uncertain significance |
| rs752259549 | 9:124,522,509 | G/A | — | uncertain significance |
| rs747142859 | 9:124,522,545 | C/T | — | uncertain significance |
| rs41273442 | 9:124,522,550 | T/C | — | benign |
| rs1441423859 | 9:124,522,627 | G/C | — | uncertain significance |
| rs150428926 | 9:124,522,649 | C/T | — | benign |
| rs1255105555 | 9:124,522,716 | A/C | — | uncertain significance |
| rs1834048881 | 9:124,525,803 | T/C | — | uncertain significance |
| rs949143587 | 9:124,525,829 | G/A | — | uncertain significance |
| rs370152633 | 9:124,525,831 | C/A | — | uncertain significance |
| rs763875376 | 9:124,525,885 | G/T | — | uncertain significance |
| rs76191175 | 9:124,526,077 | C/T | — | benign |
| rs769633331 | 9:124,526,091 | C/T | — | uncertain significance |
| rs368910721 | 9:124,526,131 | C/T | — | uncertain significance |
| rs1834291667 | 9:124,528,775 | T/G | — | uncertain significance |
| rs779618321 | 9:124,528,841 | C/T | — | uncertain significance |
| rs141771432 | 9:124,528,856 | G/A | — | uncertain significance |
| rs1230051963 | 9:124,528,952 | C/T | — | uncertain significance |
| rs1834311725 | 9:124,528,979 | A/G | — | uncertain significance |
| rs2491057073 | 9:124,530,775 | A/C | — | uncertain significance |
| rs200519908 | 9:124,530,826 | G/T | — | uncertain significance |
| rs149945931 | 9:124,530,895 | G/A | — | likely benign |
| rs771235377 | 9:124,532,832 | T/C | — | uncertain significance |
| rs753065676 | 9:124,532,900 | G/A | — | uncertain significance |
| rs199563033 | 9:124,532,937 | C/T | — | uncertain significance |
| rs532044403 | 9:124,534,974 | C/T | — | uncertain significance |
| rs759544355 | 9:124,534,987 | C/T | — | uncertain significance |
| rs2491071819 | 9:124,535,039 | G/C | — | uncertain significance |
| rs199732967 | 9:124,535,071 | G/A | — | uncertain significance |
| rs746124818 | 9:124,535,098 | C/T | — | uncertain significance |
| rs201992293 | 9:124,535,101 | C/T | — | uncertain significance |
| rs908623993 | 9:124,535,109 | G/A | — | uncertain significance |
| rs189270684 | 9:124,535,126 | T/A | — | uncertain significance |
| rs555019046 | 9:124,535,157 | G/A | — | uncertain significance |
| rs144586865 | 9:124,535,252 | C/T | — | likely benign |
| rs34458419 | 9:124,535,253 | G/A | — | benign |
| rs141593526 | 9:124,535,254 | C/T | — | uncertain significance |
| rs141810290 | 9:124,535,314 | C/T | — | uncertain significance |
| rs766855032 | 9:124,535,326 | C/T | — | uncertain significance |
| rs553670712 | 9:124,535,458 | G/A | — | uncertain significance |
| rs765138434 | 9:124,535,479 | G/A | — | uncertain significance |
| rs765361316 | 9:124,535,566 | C/T | — | uncertain significance |
| rs754653629 | 9:124,535,601 | C/T | — | uncertain significance |
| rs2119013710 | 9:124,535,605 | G/A | — | uncertain significance |
| rs373299937 | 9:124,535,655 | A/G | — | uncertain significance |
| rs1208946491 | 9:124,535,668 | C/T | — | uncertain significance |
| rs980565001 | 9:124,535,685 | T/C | — | uncertain significance |
| rs2491075046 | 9:124,535,687 | G/C | — | uncertain significance |
| rs558731616 | 9:124,535,688 | G/A | — | uncertain significance |
| rs114838746 | 9:124,535,704 | G/A | — | benign |
| rs767407304 | 9:124,535,758 | G/A | — | uncertain significance |
| rs141080470 | 9:124,536,580 | C/T | — | likely benign |
| rs1488426664 | 9:124,536,632 | C/T | — | uncertain significance |
| rs141691348 | 9:124,536,638 | C/G | — | uncertain significance |
| rs145340237 | 9:124,536,642 | C/G | — | uncertain significance |
| rs138053639 | 9:124,536,644 | C/T | — | uncertain significance |
| rs149504970 | 9:124,538,514 | C/G | — | uncertain significance |
| rs776265232 | 9:124,544,617 | G/A | — | uncertain significance |
| rs764167621 | 9:124,544,626 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.