NUP210L
nucleoporin 210 like
Summary
Predicted to act upstream of or within Sertoli cell development and spermatid development. Predicted to be located in membrane. Predicted to be part of nuclear pore. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1450941482 | 1:153,965,346 | G/A | — | uncertain significance |
| rs2526164111 | 1:153,965,347 | A/T | — | uncertain significance |
| rs549422504 | 1:153,965,411 | C/T | — | uncertain significance |
| rs369691737 | 1:153,967,627 | G/A | — | uncertain significance |
| rs370385865 | 1:153,973,383 | T/G | — | uncertain significance |
| rs1420872103 | 1:153,973,403 | T/C | — | uncertain significance |
| rs770366491 | 1:153,973,422 | C/A | — | uncertain significance |
| rs186494072 | 1:153,973,445 | T/C | — | uncertain significance |
| rs201235930 | 1:153,973,493 | T/C | — | likely benign |
| rs201672171 | 1:153,973,494 | G/T | — | uncertain significance |
| rs1462037382 | 1:153,973,512 | C/T | — | uncertain significance |
| rs2525021251 | 1:153,974,308 | G/A | — | uncertain significance |
| rs763032487 | 1:153,974,434 | C/A | — | uncertain significance |
| rs988436364 | 1:153,982,459 | C/G | — | uncertain significance |
| rs199611847 | 1:153,982,536 | C/T | — | uncertain significance |
| rs11264871 | 1:153,990,890 | A/C | intron variant | — |
| rs2525118750 | 1:153,991,452 | A/G | — | likely benign |
| rs780996708 | 1:153,991,488 | G/C | — | uncertain significance |
| rs369671902 | 1:153,994,748 | A/G | — | uncertain significance |
| rs2525140373 | 1:153,995,657 | A/G | — | likely benign |
| rs1651663591 | 1:153,995,677 | T/C | — | uncertain significance |
| rs756817954 | 1:153,995,709 | G/T | — | uncertain significance |
| rs376409501 | 1:153,998,106 | T/G | — | uncertain significance |
| rs201483933 | 1:153,998,176 | C/T | — | uncertain significance |
| rs376274427 | 1:154,000,049 | A/T | — | uncertain significance |
| rs2525178638 | 1:154,002,430 | C/G | — | uncertain significance |
| rs199925328 | 1:154,002,437 | T/C | — | uncertain significance |
| rs766659586 | 1:154,002,449 | T/C | — | uncertain significance |
| rs1653160907 | 1:154,018,579 | C/T | — | uncertain significance |
| rs2525261806 | 1:154,018,583 | T/G | — | uncertain significance |
| rs1442002255 | 1:154,018,824 | C/A | — | uncertain significance |
| rs7547009 | 1:154,019,933 | T/C | intron variant | — |
| rs1819663 | 1:154,025,891 | A/C | — | — |
| rs775208693 | 1:154,026,744 | G/A | — | uncertain significance |
| rs2525299354 | 1:154,026,882 | A/T | — | uncertain significance |
| rs758945769 | 1:154,029,349 | A/T | — | uncertain significance |
| rs2525326258 | 1:154,030,620 | A/G | — | uncertain significance |
| rs202216243 | 1:154,030,638 | G/A | — | uncertain significance |
| rs186316732 | 1:154,031,141 | G/A | — | uncertain significance |
| rs1184442890 | 1:154,033,056 | A/G | — | uncertain significance |
| rs1654082222 | 1:154,033,063 | G/T | — | uncertain significance |
| rs2525340877 | 1:154,033,429 | G/A | — | uncertain significance |
| rs200466409 | 1:154,033,471 | C/T | — | uncertain significance |
| rs2525344371 | 1:154,034,090 | A/G | — | uncertain significance |
| rs2494664 | 1:154,057,802 | A/C | — | — |
| rs72694302 | 1:154,061,787 | T/C | — | — |
| rs192877632 | 1:154,061,911 | G/A | — | uncertain significance |
| rs745360824 | 1:154,061,937 | C/A | — | uncertain significance |
| rs777495365 | 1:154,062,001 | C/G | — | uncertain significance |
| rs766498367 | 1:154,067,439 | C/T | — | uncertain significance |
| rs750022458 | 1:154,067,493 | C/T | — | likely benign |
| rs528494343 | 1:154,067,535 | C/T | — | uncertain significance |
| rs554544199 | 1:154,067,579 | C/T | — | uncertain significance |
| rs377260164 | 1:154,072,485 | C/G | — | uncertain significance |
| rs747109271 | 1:154,076,523 | A/G | — | uncertain significance |
| rs745338846 | 1:154,076,582 | T/G | — | uncertain significance |
| rs1657407726 | 1:154,090,275 | C/A | — | uncertain significance |
| rs758447806 | 1:154,090,353 | C/T | — | uncertain significance |
| rs779407203 | 1:154,091,194 | C/A | — | uncertain significance |
| rs201541774 | 1:154,091,244 | T/C | — | uncertain significance |
| rs2525618981 | 1:154,091,253 | A/T | — | uncertain significance |
| rs6671166 | 1:154,093,825 | G/A | intron variant | — |
| rs2500220 | 1:154,095,016 | C/T | intron variant | — |
| rs6692026 | 1:154,095,372 | A/G | — | — |
| rs2525662218 | 1:154,098,815 | G/C | — | uncertain significance |
| rs2494668 | 1:154,106,637 | T/C | — | — |
| rs1243881350 | 1:154,108,341 | T/C | — | uncertain significance |
| rs370316384 | 1:154,108,386 | C/T | — | uncertain significance |
| rs2494667 | 1:154,109,153 | G/T | — | — |
| rs77184519 | 1:154,110,692 | C/T | — | uncertain significance |
| rs182423356 | 1:154,112,300 | C/T | — | uncertain significance |
| rs2525733345 | 1:154,112,376 | T/G | — | uncertain significance |
| rs374512978 | 1:154,115,945 | A/G | — | uncertain significance |
| rs1281811554 | 1:154,115,969 | A/G | — | uncertain significance |
| rs1022300659 | 1:154,115,981 | C/T | — | uncertain significance |
| rs747014915 | 1:154,115,987 | C/T | — | uncertain significance |
| rs60633748 | 1:154,121,510 | T/A | — | — |
| rs3001363 | 1:154,125,067 | C/G | — | — |
| rs537647914 | 1:154,125,231 | A/C | — | uncertain significance |
| rs191237997 | 1:154,125,299 | C/A | — | uncertain significance |
| rs757259526 | 1:154,127,433 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.