RNF207
ring finger protein 207
Summary
Enables Hsp70 protein binding activity and transmembrane transporter binding activity. Involved in positive regulation of gene expression. Located in perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs927893945 | 1:6,266,600 | C/G | — | uncertain significance |
| rs373315370 | 1:6,266,669 | G/A | — | uncertain significance |
| rs140205685 | 1:6,266,696 | G/A | — | uncertain significance |
| rs1044246467 | 1:6,266,712 | C/G | — | uncertain significance |
| rs1312663755 | 1:6,266,729 | G/A | — | uncertain significance |
| rs139333535 | 1:6,266,731 | G/A | — | uncertain significance |
| rs750434674 | 1:6,266,774 | G/A | — | uncertain significance |
| rs772868363 | 1:6,267,467 | G/A | — | uncertain significance |
| rs149910082 | 1:6,267,468 | G/A | — | uncertain significance |
| rs560869444 | 1:6,267,477 | C/T | — | uncertain significance |
| rs756511425 | 1:6,267,504 | T/C | — | uncertain significance |
| rs140815362 | 1:6,267,524 | G/A | — | uncertain significance |
| rs776584581 | 1:6,267,537 | G/C | — | uncertain significance |
| rs2521322298 | 1:6,268,972 | G/A | — | uncertain significance |
| rs1434720807 | 1:6,269,220 | T/G | — | uncertain significance |
| rs372482893 | 1:6,269,224 | G/A | — | likely benign |
| rs567614508 | 1:6,269,347 | G/A | — | uncertain significance |
| rs376618138 | 1:6,269,510 | A/G | — | uncertain significance |
| rs771407150 | 1:6,269,519 | C/G | — | uncertain significance |
| rs1334836758 | 1:6,270,015 | T/C | — | uncertain significance |
| rs200803461 | 1:6,270,293 | G/A | — | uncertain significance |
| rs767660036 | 1:6,270,316 | G/T | — | uncertain significance |
| rs750819193 | 1:6,270,326 | C/T | — | uncertain significance |
| rs746281223 | 1:6,270,956 | C/G | — | uncertain significance |
| rs563500879 | 1:6,270,973 | A/C | — | uncertain significance |
| rs1214063087 | 1:6,270,993 | A/G | — | uncertain significance |
| rs748614462 | 1:6,271,139 | G/A | — | uncertain significance |
| rs367717728 | 1:6,271,144 | C/T | — | uncertain significance |
| rs569862855 | 1:6,271,145 | G/A | — | uncertain significance |
| rs552508881 | 1:6,271,179 | G/A | — | likely pathogenic |
| rs762765035 | 1:6,271,947 | C/T | — | uncertain significance |
| rs538875559 | 1:6,271,953 | C/T | — | likely benign |
| rs368957775 | 1:6,272,019 | C/T | — | uncertain significance |
| rs200938510 | 1:6,272,022 | T/G | — | uncertain significance |
| rs953899898 | 1:6,272,027 | C/T | — | uncertain significance |
| rs199839801 | 1:6,272,063 | G/C | — | uncertain significance |
| rs765413197 | 1:6,272,086 | C/G | — | uncertain significance |
| rs749955199 | 1:6,272,111 | C/T | — | uncertain significance |
| rs79344881 | 1:6,272,175 | G/A | upstream gene variant | — |
| rs202068513 | 1:6,272,364 | C/T | — | uncertain significance |
| rs776995148 | 1:6,272,387 | G/A | — | uncertain significance |
| rs755990552 | 1:6,272,420 | G/T | — | uncertain significance |
| rs375837721 | 1:6,272,429 | G/A | — | uncertain significance |
| rs747470758 | 1:6,272,433 | C/T | — | uncertain significance |
| rs1668224044 | 1:6,272,747 | G/T | — | uncertain significance |
| rs988696061 | 1:6,272,755 | C/T | — | uncertain significance |
| rs1228524733 | 1:6,272,781 | G/C | — | uncertain significance |
| rs370803462 | 1:6,273,149 | C/A | — | uncertain significance |
| rs776311499 | 1:6,273,180 | T/C | — | uncertain significance |
| rs368780534 | 1:6,273,195 | C/T | — | uncertain significance |
| rs2521394980 | 1:6,273,197 | C/T | — | uncertain significance |
| rs201905484 | 1:6,278,401 | G/A | — | uncertain significance |
| rs372042517 | 1:6,278,407 | A/G | — | uncertain significance |
| rs709209 | 1:6,278,414 | A/G | — | benign |
| rs1668465135 | 1:6,279,306 | G/A | — | uncertain significance |
| rs375833007 | 1:6,279,307 | G/C | — | uncertain significance |
| rs846111 | 1:6,279,370 | G/A | missense variant | — |
| rs748334709 | 1:6,279,435 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.