NEMP1
nuclear envelope integral membrane protein 1
Summary
Involved in nuclear membrane organization. Predicted to be located in nuclear inner membrane. Predicted to be active in nuclear envelope. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79322678 | 12:57,453,699 | C/T | — | benign |
| rs762295547 | 12:57,453,746 | A/C | — | uncertain significance |
| rs1398677893 | 12:57,453,760 | T/C | — | uncertain significance |
| rs753618647 | 12:57,454,573 | C/T | — | uncertain significance |
| rs757147384 | 12:57,454,580 | C/G | — | uncertain significance |
| rs749758386 | 12:57,454,642 | C/T | — | likely benign |
| rs2031766319 | 12:57,454,652 | C/T | — | uncertain significance |
| rs766344890 | 12:57,454,700 | C/G | — | uncertain significance |
| rs114352356 | 12:57,454,720 | C/G | — | benign |
| rs188055290 | 12:57,455,793 | T/C | intron variant | — |
| rs1304671285 | 12:57,456,953 | A/G | — | uncertain significance |
| rs777971694 | 12:57,456,959 | A/G | — | uncertain significance |
| rs767459890 | 12:57,457,058 | C/T | — | uncertain significance |
| rs2547979643 | 12:57,457,061 | T/C | — | uncertain significance |
| rs779331073 | 12:57,457,113 | C/G | — | uncertain significance |
| rs974171323 | 12:57,457,914 | T/G | — | uncertain significance |
| rs1565658642 | 12:57,458,500 | T/C | — | uncertain significance |
| rs778839804 | 12:57,463,035 | C/T | — | uncertain significance |
| rs2136508823 | 12:57,466,675 | C/G | — | uncertain significance |
| rs2547988850 | 12:57,466,678 | C/A | — | uncertain significance |
| rs2032742903 | 12:57,472,438 | G/A | — | uncertain significance |
| rs753007845 | 12:57,472,443 | C/G | — | uncertain significance |
| rs375519830 | 12:57,472,456 | C/T | — | uncertain significance |
| rs368361522 | 12:57,472,462 | C/G | — | uncertain significance |
| rs147724017 | 12:57,472,480 | G/A | — | uncertain significance |
| rs767629214 | 12:57,472,497 | G/A | — | uncertain significance |
| rs752881025 | 12:57,472,501 | A/G | — | uncertain significance |
| rs146833372 | 12:57,473,682 | T/C | upstream gene variant | — |
| rs117313188 | 12:57,480,013 | G/A | regulatory region variant | — |
| rs60667919 | 12:57,480,320 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.