POM121C
POM121 transmembrane nucleoporin C
Summary
Predicted to enable nuclear localization sequence binding activity. Predicted to be a structural constituent of nuclear pore. Predicted to be involved in RNA export from nucleus and protein import into nucleus. Located in nuclear membrane and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants114 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs782015839 | 7:75,048,096 | G/A | — | uncertain significance |
| rs236655 | 7:75,048,172 | C/T | — | likely benign |
| rs1128185 | 7:75,048,607 | C/T | — | likely benign |
| rs368251293 | 7:75,048,621 | C/T | — | uncertain significance |
| rs201815017 | 7:75,048,657 | A/G | — | uncertain significance |
| rs587604076 | 7:75,048,671 | G/A | — | uncertain significance |
| rs782082849 | 7:75,048,689 | G/A | — | uncertain significance |
| rs365436 | 7:75,048,701 | T/A | — | uncertain significance |
| rs2484224877 | 7:75,048,710 | G/T | — | uncertain significance |
| rs6465926 | 7:75,048,750 | G/T | — | — |
| rs60932781 | 7:75,049,359 | C/T | downstream gene variant | — |
| rs236660 | 7:75,050,086 | T/C | regulatory region variant | — |
| rs2484232669 | 7:75,050,811 | C/G | — | uncertain significance |
| rs782741678 | 7:75,050,842 | G/A | — | uncertain significance |
| rs236661 | 7:75,050,891 | T/C | — | likely benign |
| rs782024197 | 7:75,050,896 | G/C | — | uncertain significance |
| rs1789712254 | 7:75,050,912 | T/C | — | uncertain significance |
| rs1387609083 | 7:75,051,095 | T/C | — | uncertain significance |
| rs781838408 | 7:75,051,107 | C/G | — | uncertain significance |
| rs781873099 | 7:75,051,137 | C/T | — | uncertain significance |
| rs782434355 | 7:75,051,149 | C/T | — | likely benign |
| rs781879973 | 7:75,051,152 | C/A | — | uncertain significance |
| rs782264602 | 7:75,051,173 | C/T | — | likely benign |
| rs374096282 | 7:75,051,179 | C/T | — | likely benign |
| rs367963614 | 7:75,051,188 | C/T | — | likely benign |
| rs369777996 | 7:75,051,195 | C/T | — | likely benign |
| rs781917139 | 7:75,051,217 | G/A | — | uncertain significance |
| rs782752243 | 7:75,051,223 | G/A | — | uncertain significance |
| rs781862154 | 7:75,051,252 | C/T | — | likely benign |
| rs201428395 | 7:75,051,260 | C/T | — | uncertain significance |
| rs367547718 | 7:75,051,263 | G/A | — | uncertain significance |
| rs782333861 | 7:75,051,272 | C/G | — | uncertain significance |
| rs200158485 | 7:75,051,275 | T/C | — | uncertain significance |
| rs369177631 | 7:75,051,383 | C/T | — | likely benign |
| rs782674561 | 7:75,051,428 | G/A | — | uncertain significance |
| rs781924937 | 7:75,051,448 | G/A | — | uncertain significance |
| rs782407881 | 7:75,051,449 | G/A | — | uncertain significance |
| rs782118237 | 7:75,051,454 | G/A | — | uncertain significance |
| rs782817292 | 7:75,051,464 | C/T | — | likely benign |
| rs782753777 | 7:75,051,473 | C/G | — | uncertain significance |
| rs1431473045 | 7:75,051,490 | G/A | — | uncertain significance |
| rs2052289823 | 7:75,051,500 | T/C | — | uncertain significance |
| rs1462074396 | 7:75,051,502 | G/C | — | uncertain significance |
| rs2484235808 | 7:75,051,536 | T/G | — | uncertain significance |
| rs1789751587 | 7:75,051,544 | G/A | — | uncertain significance |
| rs1377347151 | 7:75,051,545 | C/T | — | uncertain significance |
| rs2484236004 | 7:75,051,593 | T/G | — | uncertain significance |
| rs1554470880 | 7:75,051,601 | G/A | — | uncertain significance |
| rs587695223 | 7:75,051,611 | C/T | — | uncertain significance |
| rs1185850730 | 7:75,051,649 | G/A | — | uncertain significance |
| rs1276848818 | 7:75,051,878 | C/G | — | uncertain significance |
| rs2484237369 | 7:75,052,031 | T/C | — | uncertain significance |
| rs2484237483 | 7:75,052,060 | C/T | — | uncertain significance |
| rs1554471015 | 7:75,052,067 | G/T | — | uncertain significance |
| rs379565 | 7:75,052,157 | A/G | — | uncertain significance |
| rs1554471058 | 7:75,052,202 | T/C | — | uncertain significance |
| rs1217025924 | 7:75,052,203 | C/G | — | uncertain significance |
| rs781868025 | 7:75,052,212 | A/C | — | uncertain significance |
| rs375431995 | 7:75,052,235 | C/T | — | likely benign |
| rs782409880 | 7:75,052,240 | G/T | — | uncertain significance |
| rs1394978525 | 7:75,052,271 | C/T | — | uncertain significance |
| rs1789784452 | 7:75,052,321 | A/C | — | uncertain significance |
| rs587607397 | 7:75,052,328 | G/A | — | likely benign |
| rs370098002 | 7:75,052,334 | G/A | — | uncertain significance |
| rs1554471113 | 7:75,052,352 | T/G | — | uncertain significance |
| rs587741649 | 7:75,052,391 | G/T | — | uncertain significance |
| rs781843892 | 7:75,052,423 | G/A | — | uncertain significance |
| rs1411792168 | 7:75,052,439 | G/T | — | uncertain significance |
| rs1162191146 | 7:75,052,471 | G/A | — | uncertain significance |
| rs371841804 | 7:75,053,384 | C/A | — | likely benign |
| rs416185 | 7:75,053,431 | T/G | — | benign |
| rs782238143 | 7:75,053,832 | T/C | — | uncertain significance |
| rs782133021 | 7:75,054,376 | C/T | — | uncertain significance |
| rs781793911 | 7:75,054,403 | C/T | — | uncertain significance |
| rs372375385 | 7:75,054,436 | T/C | — | uncertain significance |
| rs376008578 | 7:75,054,444 | C/T | — | likely benign |
| rs1554471639 | 7:75,054,974 | T/C | — | uncertain significance |
| rs2484250253 | 7:75,055,675 | G/C | — | uncertain significance |
| rs372291559 | 7:75,055,733 | G/G | — | benign |
| rs2484250442 | 7:75,055,735 | G/C | — | uncertain significance |
| rs236670 | 7:75,059,331 | T/G | intron variant | — |
| rs236671 | 7:75,061,419 | A/G | intron variant | — |
| rs6944634 | 7:75,061,769 | C/G | intron variant | — |
| rs371579456 | 7:75,066,836 | T/C | — | uncertain significance |
| rs587742458 | 7:75,066,839 | C/T | — | uncertain significance |
| rs369515572 | 7:75,066,845 | G/A | — | uncertain significance |
| rs427206 | 7:75,066,864 | T/C | — | uncertain significance |
| rs189506230 | 7:75,066,872 | C/T | — | likely benign |
| rs2484294798 | 7:75,066,917 | T/A | — | uncertain significance |
| rs587775631 | 7:75,066,932 | T/C | — | uncertain significance |
| rs370949929 | 7:75,068,438 | C/A | — | uncertain significance |
| rs190008034 | 7:75,068,440 | G/A | — | uncertain significance |
| rs782628966 | 7:75,068,500 | C/T | — | uncertain significance |
| rs782217655 | 7:75,068,501 | G/A | — | uncertain significance |
| rs782739335 | 7:75,070,244 | T/C | — | uncertain significance |
| rs201581797 | 7:75,070,258 | G/C | — | uncertain significance |
| rs782279658 | 7:75,070,338 | G/A | — | uncertain significance |
| rs370131057 | 7:75,070,352 | C/G | — | uncertain significance |
| rs782001232 | 7:75,070,364 | G/A | — | uncertain significance |
| rs782683976 | 7:75,070,713 | G/A | — | uncertain significance |
Showing 100 of 114 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.