ABCA10
ATP binding cassette subfamily A member 10
Summary
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. [provided by RefSeq, Jul 2008]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1370201602 | 17:67,145,026 | A/C | — | uncertain significance |
| rs1188662546 | 17:67,146,129 | C/A | — | uncertain significance |
| rs146584632 | 17:67,146,173 | C/A | — | uncertain significance |
| rs137945891 | 17:67,146,204 | T/A | — | uncertain significance |
| rs762270168 | 17:67,148,200 | C/T | — | uncertain significance |
| rs765637298 | 17:67,148,205 | G/A | — | uncertain significance |
| rs750693543 | 17:67,148,212 | G/A | — | uncertain significance |
| rs1251097041 | 17:67,148,241 | A/C | — | uncertain significance |
| rs1277563754 | 17:67,148,323 | A/G | — | uncertain significance |
| rs2074136143 | 17:67,148,521 | A/G | — | uncertain significance |
| rs377479549 | 17:67,148,603 | C/T | — | uncertain significance |
| rs201375015 | 17:67,149,465 | C/T | — | uncertain significance |
| rs145841711 | 17:67,149,540 | G/C | — | uncertain significance |
| rs768440283 | 17:67,149,650 | C/G | — | uncertain significance |
| rs146959347 | 17:67,149,666 | G/A | — | likely benign |
| rs937091663 | 17:67,150,017 | G/A | — | uncertain significance |
| rs2509381246 | 17:67,150,057 | G/A | — | uncertain significance |
| rs761135569 | 17:67,150,074 | T/C | — | uncertain significance |
| rs144160248 | 17:67,150,094 | C/G | — | uncertain significance |
| rs778354658 | 17:67,150,144 | A/C | — | uncertain significance |
| rs1052942425 | 17:67,151,250 | G/A | — | uncertain significance |
| rs140554607 | 17:67,152,011 | C/T | — | uncertain significance |
| rs150472849 | 17:67,152,020 | C/T | — | uncertain significance |
| rs537530923 | 17:67,152,031 | G/A | — | uncertain significance |
| rs374248190 | 17:67,152,992 | T/G | — | uncertain significance |
| rs1373243692 | 17:67,161,155 | T/A | — | uncertain significance |
| rs1445150582 | 17:67,161,173 | T/C | — | uncertain significance |
| rs766132609 | 17:67,170,501 | A/G | — | uncertain significance |
| rs2509406764 | 17:67,170,523 | T/C | — | uncertain significance |
| rs774182983 | 17:67,170,809 | T/C | — | uncertain significance |
| rs2509407390 | 17:67,170,813 | T/C | — | uncertain significance |
| rs750792766 | 17:67,170,846 | C/G | — | uncertain significance |
| rs150584020 | 17:67,170,870 | A/G | — | uncertain significance |
| rs142756776 | 17:67,171,593 | T/C | — | uncertain significance |
| rs1161367577 | 17:67,171,648 | T/C | — | uncertain significance |
| rs767269390 | 17:67,178,295 | C/T | — | likely benign |
| rs751033366 | 17:67,178,412 | G/C | — | uncertain significance |
| rs2509423215 | 17:67,181,657 | T/C | — | uncertain significance |
| rs2095297483 | 17:67,181,710 | T/C | — | uncertain significance |
| rs1202600814 | 17:67,181,744 | C/T | — | uncertain significance |
| rs150316122 | 17:67,181,767 | A/G | — | uncertain significance |
| rs1388474248 | 17:67,183,847 | G/A | — | uncertain significance |
| rs200565917 | 17:67,183,865 | G/C | — | uncertain significance |
| rs753872789 | 17:67,183,906 | G/A | — | uncertain significance |
| rs2509426768 | 17:67,183,937 | G/C | — | uncertain significance |
| rs139520502 | 17:67,183,939 | G/T | — | uncertain significance |
| rs138758131 | 17:67,184,008 | C/A | — | uncertain significance |
| rs146275289 | 17:67,186,600 | T/A | — | uncertain significance |
| rs781335134 | 17:67,187,325 | T/A | — | uncertain significance |
| rs776380111 | 17:67,187,395 | G/A | — | uncertain significance |
| rs904527961 | 17:67,187,449 | T/C | — | uncertain significance |
| rs2509433891 | 17:67,188,711 | G/C | — | uncertain significance |
| rs2509434193 | 17:67,188,794 | T/C | — | uncertain significance |
| rs367746608 | 17:67,189,293 | G/A | — | uncertain significance |
| rs546114873 | 17:67,189,301 | C/A | — | uncertain significance |
| rs201976695 | 17:67,189,361 | C/A | — | uncertain significance |
| rs374670778 | 17:67,189,368 | T/C | — | uncertain significance |
| rs376004282 | 17:67,189,672 | T/G | — | uncertain significance |
| rs774300123 | 17:67,189,690 | T/C | — | uncertain significance |
| rs773096533 | 17:67,190,020 | C/T | — | uncertain significance |
| rs779327397 | 17:67,190,089 | C/T | — | uncertain significance |
| rs2074483752 | 17:67,190,552 | A/G | — | uncertain significance |
| rs1568065104 | 17:67,193,244 | C/T | — | uncertain significance |
| rs148818168 | 17:67,197,668 | G/A | — | uncertain significance |
| rs766856480 | 17:67,197,675 | C/A | — | uncertain significance |
| rs2509448070 | 17:67,197,710 | T/C | — | uncertain significance |
| rs1198265411 | 17:67,210,893 | T/C | — | likely benign |
| rs1448032238 | 17:67,210,938 | C/T | — | uncertain significance |
| rs138150328 | 17:67,212,003 | C/A | — | uncertain significance |
| rs770648790 | 17:67,212,020 | G/A | — | uncertain significance |
| rs758539124 | 17:67,212,084 | C/A | — | uncertain significance |
| rs769746647 | 17:67,212,093 | C/T | — | likely benign |
| rs143678315 | 17:67,212,098 | A/G | — | uncertain significance |
| rs148511872 | 17:67,212,123 | T/C | — | uncertain significance |
| rs775160042 | 17:67,212,141 | T/G | — | uncertain significance |
| rs765715700 | 17:67,212,401 | A/G | — | uncertain significance |
| rs141867184 | 17:67,212,409 | A/T | — | uncertain significance |
| rs912698920 | 17:67,212,422 | G/A | — | uncertain significance |
| rs1179821278 | 17:67,212,426 | T/C | — | uncertain significance |
| rs776016554 | 17:67,212,457 | C/T | — | uncertain significance |
| rs560140321 | 17:67,215,774 | T/A | — | uncertain significance |
| rs143231882 | 17:67,215,836 | G/C | — | uncertain significance |
| rs2509471734 | 17:67,215,843 | A/G | — | uncertain significance |
| rs2509471741 | 17:67,215,846 | G/A | — | uncertain significance |
| rs151007615 | 17:67,218,018 | T/G | — | uncertain significance |
| rs149568652 | 17:67,218,733 | C/T | — | uncertain significance |
| rs143204065 | 17:67,218,763 | C/G | — | uncertain significance |
| rs375468801 | 17:67,218,799 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.