SSBP3
single stranded DNA binding protein 3
Summary
Predicted to enable single-stranded DNA binding activity and transcription coactivator activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be part of transcription regulator complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs553646788 | 1:54,693,972 | C/T | — | uncertain significance |
| rs776099538 | 1:54,694,446 | C/G | — | uncertain significance |
| rs752690465 | 1:54,694,489 | C/G | — | uncertain significance |
| rs142992203 | 1:54,706,582 | G/A | — | likely benign |
| rs1644651548 | 1:54,707,880 | G/A | — | uncertain significance |
| rs2525484620 | 1:54,708,957 | T/C | — | uncertain significance |
| rs151118225 | 1:54,708,960 | C/T | — | uncertain significance |
| rs608386 | 1:54,716,823 | A/T | intron variant | — |
| rs1295601669 | 1:54,717,517 | G/A | — | uncertain significance |
| rs374519094 | 1:54,722,819 | G/A | — | uncertain significance |
| rs1006253226 | 1:54,722,822 | G/A | — | uncertain significance |
| rs201068286 | 1:54,722,838 | C/T | — | uncertain significance |
| rs2523152197 | 1:54,723,782 | G/A | — | uncertain significance |
| rs562408 | 1:54,742,618 | A/G | intron variant | — |
| rs148703018 | 1:54,747,154 | T/C | — | uncertain significance |
| rs534570261 | 1:54,775,355 | G/A | — | — |
| rs192277021 | 1:54,786,625 | T/C | intron variant | — |
| rs11206341 | 1:54,831,969 | A/C | — | — |
| rs12024740 | 1:54,836,906 | A/G | intron variant | — |
| rs6699195 | 1:54,841,838 | T/C | regulatory region variant | — |
| rs12029610 | 1:54,844,602 | C/T | regulatory region variant | — |
| rs80020578 | 1:54,848,827 | G/A | intron variant | — |
| rs11206344 | 1:54,852,994 | C/A | intron variant | — |
| rs213484 | 1:54,858,872 | G/C | intron variant | — |
| rs213483 | 1:54,858,912 | G/A | — | — |
| rs213480 | 1:54,861,814 | A/G | intron variant | — |
| rs2524486775 | 1:54,870,551 | C/T | — | uncertain significance |
| rs868513221 | 1:54,871,674 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.