AQP12B
aquaporin 12B
Summary
Predicted to enable channel activity. Predicted to be involved in transmembrane transport and water transport. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1338349121 | 2:241,615,993 | C/T | — | uncertain significance |
| rs750602527 | 2:241,616,128 | C/T | — | likely benign |
| rs748167930 | 2:241,619,803 | C/A | — | uncertain significance |
| rs1240766950 | 2:241,619,820 | C/T | — | uncertain significance |
| rs770588380 | 2:241,619,822 | G/A | — | uncertain significance |
| rs200045990 | 2:241,621,659 | G/T | — | uncertain significance |
| rs1382205347 | 2:241,621,693 | T/G | — | likely benign |
| rs762167417 | 2:241,621,699 | C/T | — | uncertain significance |
| rs567002560 | 2:241,621,705 | G/T | — | uncertain significance |
| rs2536435447 | 2:241,621,744 | A/G | — | uncertain significance |
| rs752837630 | 2:241,621,753 | C/T | — | uncertain significance |
| rs549506802 | 2:241,621,785 | G/A | — | uncertain significance |
| rs771419765 | 2:241,621,788 | C/T | — | uncertain significance |
| rs1219002750 | 2:241,621,824 | T/G | — | uncertain significance |
| rs770186718 | 2:241,621,873 | G/C | — | uncertain significance |
| rs1374452728 | 2:241,621,882 | C/T | — | uncertain significance |
| rs1379106394 | 2:241,621,891 | T/C | — | likely benign |
| rs372043580 | 2:241,621,923 | G/C | — | uncertain significance |
| rs1419116939 | 2:241,621,930 | G/T | — | uncertain significance |
| rs776450045 | 2:241,621,933 | G/C | — | uncertain significance |
| rs368097369 | 2:241,621,942 | C/T | — | uncertain significance |
| rs766763215 | 2:241,621,947 | A/C | — | uncertain significance |
| rs767068318 | 2:241,621,984 | A/G | — | uncertain significance |
| rs754277716 | 2:241,621,987 | C/A | — | uncertain significance |
| rs373139392 | 2:241,621,998 | G/T | — | uncertain significance |
| rs182755222 | 2:241,622,002 | C/T | missense variant | — |
| rs374703341 | 2:241,622,010 | G/T | — | uncertain significance |
| rs376925022 | 2:241,622,011 | C/T | — | uncertain significance |
| rs750575054 | 2:241,622,029 | G/A | — | uncertain significance |
| rs200240739 | 2:241,622,061 | C/T | — | uncertain significance |
| rs747743140 | 2:241,622,062 | C/G | — | uncertain significance |
| rs573480304 | 2:241,622,074 | C/A | — | uncertain significance |
| rs770357699 | 2:241,622,113 | C/T | — | uncertain significance |
| rs959286311 | 2:241,622,133 | G/A | — | likely benign |
| rs201422028 | 2:241,622,139 | C/T | — | uncertain significance |
| rs199595129 | 2:241,622,142 | G/A | — | uncertain significance |
| rs769213334 | 2:241,622,143 | C/A | — | uncertain significance |
| rs369678598 | 2:241,622,144 | G/C | — | uncertain significance |
| rs780852278 | 2:241,622,184 | G/A | — | uncertain significance |
| rs754565566 | 2:241,622,247 | C/G | — | uncertain significance |
| rs2004007 | 2:241,622,595 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.