TMEM184B
transmembrane protein 184B
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants18 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145583176 | 22:38,617,526 | C/T | — | uncertain significance |
| rs776855728 | 22:38,617,556 | C/T | — | likely benign |
| rs150283064 | 22:38,617,570 | C/T | — | uncertain significance |
| rs2518271953 | 22:38,617,594 | G/T | — | uncertain significance |
| rs2518272444 | 22:38,617,661 | G/A | — | uncertain significance |
| rs372117761 | 22:38,617,663 | G/A | — | uncertain significance |
| rs750299549 | 22:38,617,702 | A/G | — | uncertain significance |
| rs780079876 | 22:38,617,709 | C/A | — | uncertain significance |
| rs1299626902 | 22:38,621,599 | C/T | — | uncertain significance |
| rs774661215 | 22:38,622,801 | C/T | — | uncertain significance |
| rs7289126 | 22:38,628,306 | C/A | downstream gene variant | — |
| rs2092077 | 22:38,637,808 | T/C | intron variant | — |
| rs140513108 | 22:38,642,025 | C/T | — | uncertain significance |
| rs566354338 | 22:38,643,835 | C/A | — | uncertain significance |
| rs141110992 | 22:38,643,898 | C/T | — | uncertain significance |
| rs754642953 | 22:38,643,930 | G/A | — | likely benign |
| rs756097227 | 22:38,643,957 | C/T | — | uncertain significance |
| rs75520567 | 22:38,650,488 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.