ZNF664-RFLNA
ZNF664-RFLNA readthrough
Summary
This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 664 (Gene ID: 144348) and refilin A (Gene ID: 144347) genes on chromosome 12. The read-through transcript produces a protein that shares sequence identity with the downstream refilin A gene product. [provided by RefSeq, Dec 2016]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs556992087 | 12:124,500,725 | T/C | — | — |
| rs10773049 | 12:124,506,631 | T/A | — | — |
| rs825453 | 12:124,508,758 | A/T | intron variant | — |
| rs6488915 | 12:124,511,634 | T/G | regulatory region variant | — |
| rs71458831 | 12:124,515,661 | C/T | intron variant | — |
| rs12829378 | 12:124,516,911 | G/A | regulatory region variant | — |
| rs1716403 | 12:124,519,846 | T/C | regulatory region variant | — |
| rs1996698 | 12:124,535,764 | C/T | intron variant | — |
| rs2451321 | 12:124,545,435 | G/C | intron variant | — |
| rs1716393 | 12:124,560,456 | G/T | regulatory region variant | — |
| rs825476 | 12:124,568,456 | C/A | — | — |
| rs372527826 | 12:124,577,177 | G/A | — | — |
| rs11057449 | 12:124,579,213 | G/C | intron variant | — |
| rs825499 | 12:124,580,076 | G/A | — | — |
| rs7297147 | 12:124,580,353 | A/G | intron variant | — |
| rs11057450 | 12:124,585,336 | G/C | — | — |
| rs12309254 | 12:124,585,627 | T/C | intron variant | — |
| rs11057452 | 12:124,585,946 | C/T | — | — |
| rs111668692 | 12:124,586,142 | T/C | — | — |
| rs394854 | 12:124,601,014 | A/T | — | — |
| rs424387 | 12:124,610,849 | C/G | intron variant | — |
| rs7969148 | 12:124,614,538 | T/C | intron variant | — |
| rs7311936 | 12:124,631,597 | G/A | — | — |
| rs9888360 | 12:124,645,824 | G/C | intron variant | — |
| rs10846617 | 12:124,662,131 | G/T | — | — |
| rs11057488 | 12:124,665,773 | A/G | intron variant | — |
| rs57874761 | 12:124,666,383 | A/T | — | — |
| rs7134138 | 12:124,666,527 | A/G | intron variant | — |
| rs4765353 | 12:124,667,691 | G/T | — | — |
| rs12816763 | 12:124,670,551 | G/C | intron variant | — |
| rs183910463 | 12:124,676,766 | G/A | intron variant | — |
| rs192295131 | 12:124,732,197 | G/A | intron variant | — |
| rs7961362 | 12:124,738,837 | A/T | — | — |
| rs10846636 | 12:124,743,392 | A/G | — | — |
| rs880333 | 12:124,748,860 | G/T | — | — |
| rs11057563 | 12:124,770,445 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.