ZSCAN5A
zinc finger and SCAN domain containing 5A
Summary
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199652968 | 19:56,732,954 | G/A | — | uncertain significance |
| rs2033172403 | 19:56,732,999 | C/T | — | likely benign |
| rs2033194980 | 19:56,733,086 | G/C | — | likely benign |
| rs151298410 | 19:56,733,189 | C/T | — | uncertain significance |
| rs767840197 | 19:56,733,260 | C/T | — | uncertain significance |
| rs142761513 | 19:56,733,294 | C/T | — | uncertain significance |
| rs201043563 | 19:56,733,390 | C/T | — | uncertain significance |
| rs141546124 | 19:56,733,401 | G/A | — | uncertain significance |
| rs2514227533 | 19:56,733,420 | C/T | — | uncertain significance |
| rs146066402 | 19:56,733,461 | G/A | — | uncertain significance |
| rs2514228594 | 19:56,733,477 | C/T | — | uncertain significance |
| rs575289949 | 19:56,733,503 | T/C | — | uncertain significance |
| rs773158381 | 19:56,733,507 | C/T | — | uncertain significance |
| rs757681849 | 19:56,733,545 | G/A | — | uncertain significance |
| rs369166936 | 19:56,733,549 | T/C | — | likely benign |
| rs142635871 | 19:56,733,564 | C/T | — | likely benign |
| rs770814502 | 19:56,733,579 | C/T | — | uncertain significance |
| rs750830064 | 19:56,733,612 | A/G | — | uncertain significance |
| rs2514236980 | 19:56,733,962 | G/A | — | uncertain significance |
| rs765201989 | 19:56,734,049 | G/A | — | uncertain significance |
| rs971073966 | 19:56,734,055 | A/G | — | likely benign |
| rs1343129395 | 19:56,734,058 | G/A | — | uncertain significance |
| rs977963990 | 19:56,734,060 | C/G | — | uncertain significance |
| rs376620359 | 19:56,734,071 | C/G | — | uncertain significance |
| rs149533881 | 19:56,734,077 | C/T | — | uncertain significance |
| rs375744187 | 19:56,735,070 | C/A | — | uncertain significance |
| rs746106028 | 19:56,735,106 | A/G | — | uncertain significance |
| rs139322292 | 19:56,735,119 | C/A | — | uncertain significance |
| rs2514252941 | 19:56,735,130 | C/T | — | uncertain significance |
| rs1469122932 | 19:56,735,149 | T/C | — | uncertain significance |
| rs145011101 | 19:56,735,152 | C/G | — | uncertain significance |
| rs775056079 | 19:56,736,045 | C/A | — | uncertain significance |
| rs1315010377 | 19:56,736,145 | G/C | — | uncertain significance |
| rs150925266 | 19:56,736,249 | G/A | — | uncertain significance |
| rs945144346 | 19:56,736,298 | G/A | — | uncertain significance |
| rs531042856 | 19:56,736,303 | A/C | — | uncertain significance |
| rs766292035 | 19:56,736,331 | A/C | — | uncertain significance |
| rs746372429 | 19:56,736,365 | T/G | — | uncertain significance |
| rs368670022 | 19:56,736,385 | G/C | — | uncertain significance |
| rs28369316 | 19:56,739,747 | G/C | — | benign |
| rs543259829 | 19:56,813,353 | C/G | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.