NSRP1
nuclear speckle splicing regulatory protein 1
Summary
Enables mRNA binding activity. Involved in developmental process and regulation of alternative mRNA splicing, via spliceosome. Located in nuclear speck. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773958282 | 17:28,443,863 | T/C | — | uncertain significance |
| rs761196282 | 17:28,443,871 | C/T | — | uncertain significance |
| rs868110800 | 17:28,443,872 | C/G | — | uncertain significance |
| rs6505162 | 17:28,444,183 | A/T | coding sequence variant | benign |
| rs8067576 | 17:28,444,254 | T/G | — | — |
| rs777452903 | 17:28,445,101 | T/G | — | likely pathogenic |
| rs202103242 | 17:28,445,108 | A/G | — | uncertain significance |
| rs2151869859 | 17:28,445,129 | C/T | — | uncertain significance |
| rs146976827 | 17:28,450,013 | G/A | intron variant | — |
| rs56357032 | 17:28,474,934 | A/G | — | — |
| rs187468027 | 17:28,477,775 | G/A | intron variant | — |
| rs1273379135 | 17:28,499,587 | G/A | — | uncertain significance |
| rs1005041322 | 17:28,505,109 | G/C | — | uncertain significance |
| rs143842750 | 17:28,505,167 | A/G | — | likely benign |
| rs1366669653 | 17:28,506,134 | A/C | — | uncertain significance |
| rs769451191 | 17:28,506,171 | A/G | — | uncertain significance |
| rs368966248 | 17:28,506,202 | T/A | — | uncertain significance |
| rs750680433 | 17:28,506,220 | A/C | — | uncertain significance |
| rs149526911 | 17:28,506,253 | A/C | — | uncertain significance |
| rs757684820 | 17:28,507,971 | G/A | — | uncertain significance |
| rs201919501 | 17:28,508,025 | G/A | — | uncertain significance |
| rs913173935 | 17:28,511,704 | A/G | — | uncertain significance |
| rs781089931 | 17:28,511,766 | G/A | — | uncertain significance |
| rs148657875 | 17:28,511,782 | C/T | — | uncertain significance |
| rs761957472 | 17:28,511,794 | T/C | — | uncertain significance |
| rs2509586443 | 17:28,511,922 | C/T | — | uncertain significance |
| rs561206034 | 17:28,511,996 | C/G | — | uncertain significance |
| rs147077641 | 17:28,512,013 | C/T | — | uncertain significance |
| rs770079774 | 17:28,512,019 | G/A | — | uncertain significance |
| rs1434639383 | 17:28,512,060 | G/A | — | uncertain significance |
| rs12950401 | 17:28,512,079 | A/G | — | uncertain significance |
| rs187315102 | 17:28,512,109 | C/A | — | uncertain significance |
| rs760235374 | 17:28,512,115 | C/T | — | uncertain significance |
| rs1905484438 | 17:28,512,297 | T/C | — | uncertain significance |
| rs751832321 | 17:28,512,318 | A/G | — | uncertain significance |
| rs141753156 | 17:28,512,465 | A/G | — | uncertain significance |
| rs1332989910 | 17:28,512,552 | C/A | — | uncertain significance |
| rs778726681 | 17:28,512,592 | G/A | — | uncertain significance |
| rs2509588715 | 17:28,512,673 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.