SPATS2L
spermatogenesis associated serine rich 2 like
Summary
Enables RNA binding activity. Located in cytosol; nucleolus; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs56326533 | 2:201,168,758 | T/A | — | — |
| rs10931898 | 2:201,171,191 | C/G | regulatory region variant | — |
| rs74853338 | 2:201,171,651 | C/T | regulatory region variant | — |
| rs3820888 | 2:201,180,023 | T/C | regulatory region variant | — |
| rs78681500 | 2:201,187,316 | C/T | intron variant | — |
| rs189228944 | 2:201,193,066 | T/A | intron variant | — |
| rs140001745 | 2:201,199,831 | T/G | — | — |
| rs3754797 | 2:201,242,293 | G/A | downstream gene variant | — |
| rs1020111 | 2:201,247,780 | G/T | — | — |
| rs757890707 | 2:201,253,977 | C/G | — | uncertain significance |
| rs748119026 | 2:201,284,036 | G/T | — | uncertain significance |
| rs1359788128 | 2:201,284,043 | G/T | — | uncertain significance |
| rs368695881 | 2:201,284,046 | C/G | — | uncertain significance |
| rs770203072 | 2:201,284,067 | C/T | — | uncertain significance |
| rs1574456483 | 2:201,284,110 | G/C | — | uncertain significance |
| rs200621032 | 2:201,284,192 | C/T | — | uncertain significance |
| rs1216051998 | 2:201,284,213 | G/A | — | uncertain significance |
| rs149284193 | 2:201,285,497 | A/T | intron variant | — |
| rs192861441 | 2:201,303,848 | G/A | — | likely benign |
| rs767330444 | 2:201,303,917 | G/C | — | uncertain significance |
| rs765351636 | 2:201,305,437 | G/A | — | uncertain significance |
| rs562876187 | 2:201,305,467 | G/A | — | uncertain significance |
| rs750931235 | 2:201,324,512 | C/T | — | uncertain significance |
| rs2086669559 | 2:201,332,030 | C/T | — | uncertain significance |
| rs1476824186 | 2:201,332,090 | A/T | — | uncertain significance |
| rs753086619 | 2:201,334,679 | G/A | — | uncertain significance |
| rs754826654 | 2:201,334,683 | C/T | — | uncertain significance |
| rs2469734998 | 2:201,334,712 | A/G | — | uncertain significance |
| rs1402911390 | 2:201,337,639 | G/A | — | uncertain significance |
| rs750637147 | 2:201,337,708 | C/G | — | uncertain significance |
| rs372733147 | 2:201,342,361 | T/G | — | uncertain significance |
| rs2469804840 | 2:201,342,363 | G/C | — | uncertain significance |
| rs555931476 | 2:201,342,380 | C/T | — | uncertain significance |
| rs755624056 | 2:201,342,482 | C/A | — | uncertain significance |
| rs768329685 | 2:201,342,485 | G/A | — | uncertain significance |
| rs1044985765 | 2:201,342,500 | C/T | — | uncertain significance |
| rs1342966326 | 2:201,342,501 | C/T | — | uncertain significance |
| rs773298087 | 2:201,342,503 | C/T | — | uncertain significance |
| rs776803024 | 2:201,342,509 | G/A | — | uncertain significance |
| rs751895129 | 2:201,342,630 | C/T | — | uncertain significance |
| rs767684719 | 2:201,342,647 | C/G | — | uncertain significance |
| rs2469808582 | 2:201,342,660 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.