SPATA13
spermatogenesis associated 13
Summary
Enables guanyl-nucleotide exchange factor activity and identical protein binding activity. Involved in cell migration; plasma membrane bounded cell projection assembly; and regulation of cell migration. Located in several cellular components, including filopodium; lamellipodium; and ruffle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants125 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17079773 | 13:24,598,384 | C/T | intron variant | — |
| rs4769312 | 13:24,623,220 | G/A | intron variant | — |
| rs17079928 | 13:24,654,228 | G/A | intron variant | — |
| rs9805786 | 13:24,658,356 | G/T | intron variant | — |
| rs9507279 | 13:24,775,834 | C/G | — | — |
| rs7329958 | 13:24,782,080 | T/C | intron variant | — |
| rs7326088 | 13:24,782,963 | C/G | — | — |
| rs9507285 | 13:24,784,888 | C/T | — | — |
| rs7321973 | 13:24,785,603 | C/A | intron variant | — |
| rs7327979 | 13:24,786,069 | A/G | intron variant | — |
| rs7327883 | 13:24,786,385 | C/T | intron variant | — |
| rs9511151 | 13:24,786,576 | G/A | intron variant | — |
| rs9507287 | 13:24,786,577 | T/C | intron variant | — |
| rs715921 | 13:24,795,489 | G/C | — | — |
| rs146799878 | 13:24,797,007 | C/T | — | benign |
| rs768743626 | 13:24,797,075 | A/G | — | uncertain significance |
| rs896391576 | 13:24,797,083 | G/A | — | uncertain significance |
| rs1360433813 | 13:24,797,087 | G/A | — | uncertain significance |
| rs376486791 | 13:24,797,111 | A/G | — | uncertain significance |
| rs564986010 | 13:24,797,137 | G/A | — | uncertain significance |
| rs1871689253 | 13:24,797,153 | C/T | — | uncertain significance |
| rs369711697 | 13:24,797,169 | G/A | — | likely benign |
| rs1313171903 | 13:24,797,191 | G/A | — | uncertain significance |
| rs966488124 | 13:24,797,200 | C/T | — | uncertain significance |
| rs529939542 | 13:24,797,218 | G/A | — | uncertain significance |
| rs979566547 | 13:24,797,241 | C/T | — | likely benign |
| rs369038043 | 13:24,797,258 | A/T | — | uncertain significance |
| rs1383899872 | 13:24,797,285 | T/C | — | uncertain significance |
| rs1220545 | 13:24,797,333 | G/C | — | benign |
| rs565858739 | 13:24,797,450 | G/A | — | uncertain significance |
| rs2541910607 | 13:24,797,462 | A/T | — | uncertain significance |
| rs534848376 | 13:24,797,485 | T/G | — | uncertain significance |
| rs372376733 | 13:24,797,486 | C/T | — | likely benign |
| rs1298609255 | 13:24,797,563 | C/G | — | uncertain significance |
| rs150850951 | 13:24,797,564 | C/T | — | likely benign |
| rs1363778088 | 13:24,797,567 | G/T | — | uncertain significance |
| rs2541911238 | 13:24,797,590 | C/T | — | uncertain significance |
| rs1242648956 | 13:24,797,646 | C/A | — | uncertain significance |
| rs1243069895 | 13:24,797,677 | C/T | — | uncertain significance |
| rs760982297 | 13:24,797,678 | G/A | — | uncertain significance |
| rs1191227821 | 13:24,797,774 | A/G | — | uncertain significance |
| rs376505603 | 13:24,797,781 | C/T | — | likely benign |
| rs1421891561 | 13:24,797,835 | C/G | — | uncertain significance |
| rs1437063318 | 13:24,797,857 | A/G | — | uncertain significance |
| rs1385735564 | 13:24,797,896 | C/T | — | uncertain significance |
| rs1326018937 | 13:24,797,902 | A/G | — | uncertain significance |
| rs751634344 | 13:24,797,907 | C/T | — | likely benign |
| rs1435245095 | 13:24,797,951 | C/T | — | uncertain significance |
| rs528560969 | 13:24,798,080 | G/A | — | likely benign |
| rs1028386964 | 13:24,798,133 | C/T | — | uncertain significance |
| rs748926871 | 13:24,798,139 | C/T | — | uncertain significance |
| rs1871776003 | 13:24,798,148 | T/C | — | uncertain significance |
| rs866164938 | 13:24,798,191 | G/A | — | uncertain significance |
| rs11842597 | 13:24,798,221 | C/T | — | benign |
| rs759669966 | 13:24,798,232 | G/A | — | uncertain significance |
| rs1048698814 | 13:24,798,239 | C/G | — | uncertain significance |
| rs1195473389 | 13:24,798,259 | T/C | — | uncertain significance |
| rs750078906 | 13:24,798,434 | A/G | — | uncertain significance |
| rs2541915228 | 13:24,798,464 | C/T | — | uncertain significance |
| rs779591912 | 13:24,798,468 | C/T | — | likely benign |
| rs41314440 | 13:24,798,506 | C/T | — | benign |
| rs1040921987 | 13:24,798,508 | G/A | — | uncertain significance |
| rs372768109 | 13:24,798,632 | T/C | — | uncertain significance |
| rs571099862 | 13:24,798,700 | G/A | — | uncertain significance |
| rs527302064 | 13:24,823,618 | G/A | — | uncertain significance |
| rs1487073013 | 13:24,823,622 | C/G | — | uncertain significance |
| rs770688821 | 13:24,823,631 | C/T | — | uncertain significance |
| rs753950569 | 13:24,823,711 | C/T | — | uncertain significance |
| rs1469418948 | 13:24,823,731 | C/A | — | likely benign |
| rs1873360419 | 13:24,823,739 | A/G | — | uncertain significance |
| rs549702506 | 13:24,823,748 | T/C | — | uncertain significance |
| rs745702947 | 13:24,823,810 | C/T | — | uncertain significance |
| rs201659176 | 13:24,823,832 | C/A | — | uncertain significance |
| rs766640323 | 13:24,823,886 | A/G | — | likely benign |
| rs143963425 | 13:24,823,892 | C/A | — | uncertain significance |
| rs7330736 | 13:24,823,894 | T/C | — | benign |
| rs762897184 | 13:24,823,903 | C/T | — | uncertain significance |
| rs80073311 | 13:24,823,928 | C/T | — | benign |
| rs543934868 | 13:24,823,952 | C/T | — | likely benign |
| rs2541976299 | 13:24,823,961 | T/C | — | uncertain significance |
| rs765118612 | 13:24,825,857 | C/T | — | uncertain significance |
| rs142261154 | 13:24,825,965 | G/A | — | uncertain significance |
| rs750437771 | 13:24,825,973 | C/T | — | uncertain significance |
| rs773438885 | 13:24,825,974 | G/A | — | uncertain significance |
| rs745333635 | 13:24,825,977 | G/A | — | uncertain significance |
| rs776877407 | 13:24,825,979 | C/T | — | uncertain significance |
| rs35768526 | 13:24,844,994 | G/C | — | benign |
| rs778961788 | 13:24,858,288 | G/T | — | uncertain significance |
| rs990477708 | 13:24,858,342 | A/G | — | uncertain significance |
| rs376912782 | 13:24,858,369 | G/A | — | uncertain significance |
| rs770276802 | 13:24,860,365 | G/T | — | uncertain significance |
| rs749386397 | 13:24,860,439 | G/T | — | uncertain significance |
| rs768852418 | 13:24,860,449 | A/T | — | uncertain significance |
| rs142906131 | 13:24,860,487 | C/T | — | uncertain significance |
| rs578230480 | 13:24,860,965 | C/T | — | likely benign |
| rs1231290257 | 13:24,861,014 | A/T | — | uncertain significance |
| rs568317408 | 13:24,861,024 | A/G | — | uncertain significance |
| rs1875993202 | 13:24,861,055 | G/C | — | likely benign |
| rs566635972 | 13:24,861,096 | G/A | — | likely benign |
| rs781461627 | 13:24,863,130 | T/C | — | likely benign |
Showing 100 of 125 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.