ABCC10
ATP binding cassette subfamily C member 10
Summary
The 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 intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This ABC full-transporter is a member of the MRP subfamily which is involved in multi-drug resistance. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2010]
Known Variants96 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200304551 | 6:43,399,880 | G/C | — | uncertain significance |
| rs375497152 | 6:43,399,917 | C/T | — | uncertain significance |
| rs1781219005 | 6:43,399,995 | G/T | — | uncertain significance |
| rs2481036499 | 6:43,399,999 | G/T | — | uncertain significance |
| rs371981738 | 6:43,400,059 | G/A | — | uncertain significance |
| rs149850309 | 6:43,400,073 | C/G | — | uncertain significance |
| rs1327817713 | 6:43,400,110 | G/A | — | uncertain significance |
| rs755902038 | 6:43,400,241 | C/G | — | uncertain significance |
| rs1474713207 | 6:43,400,317 | C/T | — | uncertain significance |
| rs866559994 | 6:43,400,325 | C/G | — | uncertain significance |
| rs1288129776 | 6:43,400,383 | C/T | — | uncertain significance |
| rs147440117 | 6:43,400,406 | G/C | — | uncertain significance |
| rs759559074 | 6:43,400,572 | A/G | — | uncertain significance |
| rs202203665 | 6:43,400,598 | G/A | — | uncertain significance |
| rs555034468 | 6:43,400,760 | G/A | — | uncertain significance |
| rs1323291348 | 6:43,400,874 | A/C | — | uncertain significance |
| rs528202255 | 6:43,400,886 | C/G | — | uncertain significance |
| rs185652890 | 6:43,400,887 | G/A | — | uncertain significance |
| rs998376744 | 6:43,401,006 | G/C | — | uncertain significance |
| rs758290484 | 6:43,401,046 | G/A | — | uncertain significance |
| rs1781336684 | 6:43,401,058 | G/A | — | uncertain significance |
| rs746806212 | 6:43,401,070 | T/C | — | uncertain significance |
| rs138248684 | 6:43,401,090 | C/T | missense variant | — |
| rs751655535 | 6:43,402,386 | C/T | — | uncertain significance |
| rs2481052051 | 6:43,402,425 | G/T | — | uncertain significance |
| rs2481052402 | 6:43,402,475 | C/G | — | uncertain significance |
| rs543886430 | 6:43,402,489 | C/T | — | uncertain significance |
| rs200774822 | 6:43,402,490 | G/A | — | likely benign |
| rs1231790897 | 6:43,402,522 | T/C | — | uncertain significance |
| rs200663342 | 6:43,402,561 | T/C | — | uncertain significance |
| rs1781510422 | 6:43,402,567 | A/G | — | uncertain significance |
| rs779079010 | 6:43,403,493 | T/A | — | uncertain significance |
| rs2481061149 | 6:43,403,520 | T/C | — | uncertain significance |
| rs1386075700 | 6:43,403,555 | A/T | — | uncertain significance |
| rs762674596 | 6:43,403,606 | G/A | — | uncertain significance |
| rs535397254 | 6:43,403,625 | C/T | — | uncertain significance |
| rs2481065220 | 6:43,403,932 | G/A | — | uncertain significance |
| rs758378679 | 6:43,405,684 | G/C | — | uncertain significance |
| rs1372266163 | 6:43,406,400 | G/C | — | uncertain significance |
| rs768956566 | 6:43,406,520 | A/G | — | uncertain significance |
| rs67861980 | 6:43,408,105 | C/T | intron variant | — |
| rs1490120138 | 6:43,409,612 | G/A | — | uncertain significance |
| rs777887477 | 6:43,409,615 | G/T | — | uncertain significance |
| rs770817341 | 6:43,409,619 | A/G | — | uncertain significance |
| rs1053808601 | 6:43,409,626 | G/T | — | uncertain significance |
| rs772818379 | 6:43,410,727 | T/C | — | uncertain significance |
| rs770288857 | 6:43,410,736 | C/T | — | uncertain significance |
| rs764506403 | 6:43,410,847 | A/G | — | uncertain significance |
| rs752167077 | 6:43,410,853 | C/G | — | uncertain significance |
| rs201247634 | 6:43,410,860 | G/A | — | likely benign |
| rs371967874 | 6:43,410,882 | C/T | — | uncertain significance |
| rs767098942 | 6:43,410,892 | G/A | — | likely benign |
| rs775614402 | 6:43,411,738 | G/C | — | uncertain significance |
| rs369336854 | 6:43,411,739 | T/C | — | uncertain significance |
| rs760290118 | 6:43,411,939 | G/A | — | uncertain significance |
| rs148750882 | 6:43,411,941 | C/A | — | uncertain significance |
| rs1416436688 | 6:43,412,004 | G/A | — | uncertain significance |
| rs773004616 | 6:43,412,084 | C/G | — | likely benign |
| rs761231615 | 6:43,412,531 | C/T | — | uncertain significance |
| rs142977044 | 6:43,412,612 | A/C | — | uncertain significance |
| rs201909610 | 6:43,412,629 | G/C | — | uncertain significance |
| rs200602946 | 6:43,412,898 | A/G | — | uncertain significance |
| rs2481162268 | 6:43,412,910 | A/G | — | uncertain significance |
| rs988985931 | 6:43,412,939 | A/T | — | uncertain significance |
| rs767665063 | 6:43,412,942 | A/G | — | uncertain significance |
| rs780591615 | 6:43,413,024 | A/G | — | uncertain significance |
| rs2481168886 | 6:43,413,383 | A/G | — | uncertain significance |
| rs2481169102 | 6:43,413,395 | C/T | — | uncertain significance |
| rs774021762 | 6:43,413,476 | T/A | — | uncertain significance |
| rs199502499 | 6:43,413,481 | G/A | — | uncertain significance |
| rs772901325 | 6:43,413,491 | C/G | — | uncertain significance |
| rs1309285151 | 6:43,413,535 | A/G | — | uncertain significance |
| rs773675473 | 6:43,413,583 | C/T | — | uncertain significance |
| rs530304629 | 6:43,413,587 | G/T | — | uncertain significance |
| rs535032639 | 6:43,413,659 | G/A | — | uncertain significance |
| rs776953080 | 6:43,413,674 | C/T | — | uncertain significance |
| rs2481177922 | 6:43,414,085 | C/A | — | uncertain significance |
| rs151166248 | 6:43,414,133 | G/A | — | uncertain significance |
| rs1214747 | 6:43,414,234 | G/C | downstream gene variant | — |
| rs561577186 | 6:43,415,037 | C/T | — | uncertain significance |
| rs779288383 | 6:43,415,039 | G/C | — | uncertain significance |
| rs2481190627 | 6:43,415,074 | G/C | — | uncertain significance |
| rs745792705 | 6:43,415,087 | G/A | — | uncertain significance |
| rs148109801 | 6:43,415,145 | A/G | — | uncertain significance |
| rs6901992 | 6:43,415,429 | C/T | — | benign |
| rs768463841 | 6:43,415,431 | G/A | — | uncertain significance |
| rs375963017 | 6:43,415,624 | G/A | — | uncertain significance |
| rs573450847 | 6:43,415,638 | G/A | — | uncertain significance |
| rs535694701 | 6:43,415,641 | G/A | — | uncertain significance |
| rs764754258 | 6:43,416,666 | C/G | — | uncertain significance |
| rs199697720 | 6:43,416,671 | C/T | — | uncertain significance |
| rs768431659 | 6:43,416,762 | T/C | — | uncertain significance |
| rs772941955 | 6:43,416,941 | A/G | — | uncertain significance |
| rs367985559 | 6:43,417,199 | A/G | — | uncertain significance |
| rs775939054 | 6:43,417,227 | T/C | — | uncertain significance |
| rs527438657 | 6:43,417,759 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.