CSRNP3
cysteine and serine rich nuclear protein 3
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in positive regulation of apoptotic process and positive regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6432832 | 2:166,370,826 | A/T | — | — |
| rs112396755 | 2:166,416,341 | A/G | intron variant | — |
| rs199893751 | 2:166,451,615 | G/A | — | uncertain significance |
| rs1208527019 | 2:166,451,633 | T/C | — | uncertain significance |
| rs770309060 | 2:166,514,411 | C/T | — | uncertain significance |
| rs140972706 | 2:166,522,054 | G/A | intron variant | — |
| rs559756288 | 2:166,532,865 | T/C | — | uncertain significance |
| rs2468032410 | 2:166,532,906 | A/G | — | uncertain significance |
| rs769777169 | 2:166,532,922 | A/C | — | uncertain significance |
| rs2468032886 | 2:166,533,101 | G/A | — | uncertain significance |
| rs1248814234 | 2:166,535,357 | A/C | — | uncertain significance |
| rs773545370 | 2:166,535,391 | A/G | — | uncertain significance |
| rs760156809 | 2:166,535,421 | G/A | — | uncertain significance |
| rs758424330 | 2:166,535,460 | A/G | — | uncertain significance |
| rs1687476379 | 2:166,535,481 | G/T | — | uncertain significance |
| rs2468035758 | 2:166,535,546 | G/C | — | uncertain significance |
| rs3731765 | 2:166,535,588 | G/A | — | benign |
| rs375174523 | 2:166,535,669 | C/T | — | likely benign |
| rs761212722 | 2:166,535,682 | T/C | — | uncertain significance |
| rs751554858 | 2:166,535,692 | G/A | — | uncertain significance |
| rs750565651 | 2:166,535,712 | G/C | — | uncertain significance |
| rs1331342423 | 2:166,535,715 | G/T | — | uncertain significance |
| rs780332011 | 2:166,535,730 | G/C | — | uncertain significance |
| rs747366779 | 2:166,535,731 | T/G | — | uncertain significance |
| rs149031589 | 2:166,535,756 | C/A | — | benign |
| rs1216306223 | 2:166,535,796 | A/C | — | uncertain significance |
| rs143480423 | 2:166,535,852 | G/T | — | uncertain significance |
| rs891094004 | 2:166,535,875 | G/A | — | uncertain significance |
| rs1397540267 | 2:166,535,880 | A/C | — | uncertain significance |
| rs373694116 | 2:166,535,950 | G/A | — | uncertain significance |
| rs1687494030 | 2:166,536,046 | C/T | — | uncertain significance |
| rs779602441 | 2:166,536,208 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.