NASP
nuclear autoantigenic sperm protein
Summary
This gene encodes a H1 histone binding protein that is involved in transporting histones into the nucleus of dividing cells. Multiple isoforms are encoded by transcript variants of this gene. The somatic form is expressed in all mitotic cells, is localized to the nucleus, and is coupled to the cell cycle. The testicular form is expressed in embryonic tissues, tumor cells, and the testis. In male germ cells, this protein is localized to the cytoplasm of primary spermatocytes, the nucleus of spermatids, and the periacrosomal region of mature spermatozoa. [provided by RefSeq, Jul 2008]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs763559571 | 1:46,049,870 | G/C | — | uncertain significance |
| rs757741104 | 1:46,056,905 | G/A | — | uncertain significance |
| rs2523155742 | 1:46,056,918 | C/G | — | uncertain significance |
| rs1211353839 | 1:46,067,976 | C/T | — | uncertain significance |
| rs371938635 | 1:46,070,633 | A/G | — | uncertain significance |
| rs1643910615 | 1:46,072,183 | T/G | — | uncertain significance |
| rs769592053 | 1:46,073,030 | C/A | — | uncertain significance |
| rs373922767 | 1:46,073,050 | A/C | — | uncertain significance |
| rs200782827 | 1:46,073,088 | G/A | — | uncertain significance |
| rs144479143 | 1:46,073,109 | A/G | — | uncertain significance |
| rs143372420 | 1:46,073,110 | G/T | — | uncertain significance |
| rs2521955963 | 1:46,073,147 | A/G | — | uncertain significance |
| rs112075833 | 1:46,073,168 | A/C | — | benign |
| rs924499416 | 1:46,073,224 | A/G | — | uncertain significance |
| rs758161978 | 1:46,073,248 | C/T | — | likely benign |
| rs2521958089 | 1:46,073,293 | C/T | — | uncertain significance |
| rs1051618587 | 1:46,073,295 | G/C | — | uncertain significance |
| rs201684799 | 1:46,073,341 | A/C | — | uncertain significance |
| rs746326050 | 1:46,073,344 | G/A | — | likely benign |
| rs887352700 | 1:46,073,366 | G/T | — | uncertain significance |
| rs1643932834 | 1:46,073,400 | A/G | — | uncertain significance |
| rs1643933832 | 1:46,073,439 | C/G | — | likely benign |
| rs759459986 | 1:46,073,523 | C/T | — | uncertain significance |
| rs535215279 | 1:46,073,566 | C/G | — | uncertain significance |
| rs147021326 | 1:46,073,628 | A/G | — | uncertain significance |
| rs777990611 | 1:46,073,677 | A/G | — | uncertain significance |
| rs560873126 | 1:46,073,716 | G/A | — | uncertain significance |
| rs528141974 | 1:46,073,725 | A/G | — | uncertain significance |
| rs761712731 | 1:46,073,731 | C/T | — | likely benign |
| rs1643940980 | 1:46,073,748 | C/G | — | uncertain significance |
| rs1364277074 | 1:46,073,757 | A/G | — | likely benign |
| rs758485797 | 1:46,073,805 | T/C | — | uncertain significance |
| rs768455377 | 1:46,073,818 | A/G | — | uncertain significance |
| rs777015518 | 1:46,073,946 | A/G | — | uncertain significance |
| rs2522036937 | 1:46,079,996 | G/A | — | uncertain significance |
| rs2522045517 | 1:46,080,742 | A/G | — | uncertain significance |
| rs147650410 | 1:46,080,844 | A/G | — | uncertain significance |
| rs144435495 | 1:46,080,849 | A/G | — | likely benign |
| rs778838858 | 1:46,080,854 | A/C | — | uncertain significance |
| rs2522049125 | 1:46,081,042 | G/A | — | uncertain significance |
| rs199692248 | 1:46,081,063 | G/A | — | uncertain significance |
| rs2522049349 | 1:46,081,066 | A/G | — | uncertain significance |
| rs147979968 | 1:46,081,103 | G/A | — | likely benign |
| rs769590735 | 1:46,081,105 | A/T | — | uncertain significance |
| rs780636281 | 1:46,083,141 | C/A | — | uncertain significance |
| rs140761967 | 1:46,083,193 | C/T | — | uncertain significance |
| rs369875644 | 1:46,083,200 | G/A | — | likely benign |
| rs773012602 | 1:46,083,213 | G/A | — | uncertain significance |
| rs1569626639 | 1:46,083,225 | C/T | — | likely benign |
| rs749672551 | 1:46,083,244 | C/T | — | uncertain significance |
| rs770749858 | 1:46,083,754 | C/T | — | uncertain significance |
| rs376271232 | 1:46,084,084 | T/C | — | — |
| rs1053941 | 1:46,084,383 | G/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.