RNF10
ring finger protein 10
Summary
The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747471809 | 12:120,972,645 | A/G | — | uncertain significance |
| rs1327493457 | 12:120,972,667 | A/G | — | uncertain significance |
| rs763196486 | 12:120,972,671 | C/A | — | uncertain significance |
| rs2500609060 | 12:120,972,679 | A/G | — | likely benign |
| rs2500609154 | 12:120,972,696 | T/A | — | uncertain significance |
| rs377054423 | 12:120,972,756 | T/G | — | uncertain significance |
| rs614226 | 12:120,974,510 | C/T | regulatory region variant | — |
| rs376427405 | 12:120,984,235 | G/A | — | uncertain significance |
| rs111483466 | 12:120,984,244 | G/A | — | uncertain significance |
| rs765706820 | 12:120,984,271 | A/G | — | uncertain significance |
| rs748131170 | 12:120,984,297 | C/T | — | uncertain significance |
| rs201217014 | 12:120,984,337 | C/T | — | uncertain significance |
| rs1021762197 | 12:120,984,342 | C/G | — | uncertain significance |
| rs141915839 | 12:120,984,354 | G/A | — | uncertain significance |
| rs1368935610 | 12:120,984,383 | T/C | — | likely benign |
| rs2137176791 | 12:120,990,335 | G/A | — | uncertain significance |
| rs370551365 | 12:120,990,360 | T/A | — | uncertain significance |
| rs746773965 | 12:120,990,408 | C/T | — | uncertain significance |
| rs200200679 | 12:120,992,526 | A/G | — | uncertain significance |
| rs142763100 | 12:120,995,118 | A/G | — | uncertain significance |
| rs778352149 | 12:120,995,131 | C/T | — | uncertain significance |
| rs765765405 | 12:120,995,368 | C/T | — | uncertain significance |
| rs200683852 | 12:120,995,396 | C/T | — | uncertain significance |
| rs1315787464 | 12:120,995,402 | A/G | — | uncertain significance |
| rs1565958515 | 12:120,995,422 | G/A | — | uncertain significance |
| rs1321194429 | 12:120,998,579 | G/T | — | uncertain significance |
| rs769630404 | 12:120,998,597 | C/G | — | uncertain significance |
| rs585510 | 12:121,000,133 | A/T | — | — |
| rs2500746437 | 12:121,000,757 | G/A | — | uncertain significance |
| rs146309808 | 12:121,000,767 | C/G | — | uncertain significance |
| rs116727495 | 12:121,000,778 | G/A | — | benign |
| rs752289695 | 12:121,000,851 | A/G | — | uncertain significance |
| rs2500749499 | 12:121,001,265 | A/T | — | uncertain significance |
| rs369715030 | 12:121,001,279 | G/A | — | uncertain significance |
| rs768056108 | 12:121,001,316 | A/G | — | uncertain significance |
| rs1593100135 | 12:121,001,337 | C/G | — | uncertain significance |
| rs1875238043 | 12:121,001,396 | A/C | — | uncertain significance |
| rs935309256 | 12:121,001,418 | T/A | — | uncertain significance |
| rs377456759 | 12:121,001,712 | C/T | — | uncertain significance |
| rs112788889 | 12:121,002,412 | A/C | intron variant | — |
| rs752189774 | 12:121,003,285 | G/A | — | uncertain significance |
| rs1451237738 | 12:121,004,666 | T/C | — | uncertain significance |
| rs763431421 | 12:121,004,684 | T/C | — | uncertain significance |
| rs751352713 | 12:121,004,715 | C/T | — | uncertain significance |
| rs1868968133 | 12:121,004,742 | T/A | — | uncertain significance |
| rs761359348 | 12:121,004,753 | C/T | — | uncertain significance |
| rs1187356807 | 12:121,008,999 | C/A | — | uncertain significance |
| rs770014286 | 12:121,013,604 | G/A | — | uncertain significance |
| rs752952458 | 12:121,013,621 | C/T | — | uncertain significance |
| rs767509811 | 12:121,013,633 | G/A | — | uncertain significance |
| rs3817301 | 12:121,014,027 | G/A | downstream gene variant | — |
| rs557358257 | 12:121,014,411 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.