PRRT3
proline rich transmembrane protein 3
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs770045739 | 3:9,987,943 | G/C | — | uncertain significance |
| rs1030465121 | 3:9,987,993 | T/C | — | uncertain significance |
| rs759375218 | 3:9,988,069 | G/A | — | uncertain significance |
| rs2470535561 | 3:9,988,077 | T/C | — | uncertain significance |
| rs1329492229 | 3:9,988,153 | T/C | — | uncertain significance |
| rs2470535969 | 3:9,988,156 | C/T | — | uncertain significance |
| rs2085524215 | 3:9,988,200 | T/C | — | uncertain significance |
| rs909804737 | 3:9,988,209 | G/C | — | uncertain significance |
| rs2470536523 | 3:9,988,252 | G/A | — | uncertain significance |
| rs367595627 | 3:9,988,302 | C/G | — | uncertain significance |
| rs781667889 | 3:9,988,321 | C/T | — | uncertain significance |
| rs377716668 | 3:9,988,323 | C/T | — | uncertain significance |
| rs1418251842 | 3:9,988,336 | A/G | — | uncertain significance |
| rs763313437 | 3:9,988,380 | A/G | — | uncertain significance |
| rs376131676 | 3:9,988,419 | C/A | — | uncertain significance |
| rs371533970 | 3:9,988,512 | G/A | — | uncertain significance |
| rs756695094 | 3:9,988,515 | C/G | — | uncertain significance |
| rs757915265 | 3:9,988,523 | C/G | — | uncertain significance |
| rs1364373547 | 3:9,988,591 | G/A | — | uncertain significance |
| rs1056772192 | 3:9,988,626 | C/A | — | uncertain significance |
| rs2470538251 | 3:9,988,629 | A/T | — | uncertain significance |
| rs372155025 | 3:9,988,701 | G/A | — | uncertain significance |
| rs1300469696 | 3:9,988,756 | C/A | — | uncertain significance |
| rs368700883 | 3:9,988,767 | G/T | — | uncertain significance |
| rs1385134956 | 3:9,988,968 | C/A | — | uncertain significance |
| rs201765414 | 3:9,988,989 | C/T | — | uncertain significance |
| rs950776667 | 3:9,989,100 | A/G | — | uncertain significance |
| rs377041596 | 3:9,989,323 | C/A | — | uncertain significance |
| rs779355483 | 3:9,989,355 | C/T | — | uncertain significance |
| rs747416534 | 3:9,989,430 | T/C | — | uncertain significance |
| rs761513300 | 3:9,989,453 | G/C | — | uncertain significance |
| rs2085553899 | 3:9,989,457 | A/C | — | uncertain significance |
| rs375628005 | 3:9,989,475 | C/A | — | uncertain significance |
| rs1021322443 | 3:9,989,477 | C/G | — | uncertain significance |
| rs765548493 | 3:9,989,493 | G/A | — | uncertain significance |
| rs752136487 | 3:9,989,526 | G/T | — | uncertain significance |
| rs770637558 | 3:9,989,556 | G/A | — | uncertain significance |
| rs761781047 | 3:9,989,608 | G/A | — | uncertain significance |
| rs1308555677 | 3:9,989,638 | G/T | — | uncertain significance |
| rs778331758 | 3:9,989,652 | C/G | — | uncertain significance |
| rs1275941809 | 3:9,989,667 | G/A | — | uncertain significance |
| rs909458664 | 3:9,989,677 | C/T | — | uncertain significance |
| rs754608915 | 3:9,990,459 | A/T | — | uncertain significance |
| rs772318958 | 3:9,990,507 | G/A | — | uncertain significance |
| rs375040878 | 3:9,990,541 | C/T | — | uncertain significance |
| rs187203537 | 3:9,990,555 | C/T | — | uncertain significance |
| rs59465469 | 3:9,990,800 | G/A | missense variant | — |
| rs147199463 | 3:9,990,809 | C/A | — | uncertain significance |
| rs777959953 | 3:9,990,845 | G/A | — | uncertain significance |
| rs749827983 | 3:9,990,857 | C/T | — | uncertain significance |
| rs199781229 | 3:9,990,863 | G/T | — | uncertain significance |
| rs200982741 | 3:9,990,895 | G/A | — | likely benign |
| rs187933089 | 3:9,991,040 | A/G | — | uncertain significance |
| rs376347886 | 3:9,991,218 | G/T | — | uncertain significance |
| rs776827403 | 3:9,991,249 | C/T | — | uncertain significance |
| rs199883920 | 3:9,991,352 | G/A | — | uncertain significance |
| rs756099079 | 3:9,991,559 | C/T | — | uncertain significance |
| rs775805094 | 3:9,991,574 | G/A | — | uncertain significance |
| rs377172137 | 3:9,991,588 | C/T | — | uncertain significance |
| rs371615441 | 3:9,991,615 | G/A | — | likely benign |
| rs2470551387 | 3:9,991,699 | A/G | — | uncertain significance |
| rs748738177 | 3:9,991,789 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.