VRTN
vertebrae development associated
Summary
Predicted to enable sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be active in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138920255 | 14:74,795,855 | G/A | intron variant | — |
| rs148216033 | 14:74,799,677 | C/T | intron variant | — |
| rs577330509 | 14:74,799,915 | G/T | — | — |
| rs533283089 | 14:74,806,949 | G/A | — | — |
| rs2506030479 | 14:74,823,529 | C/A | — | uncertain significance |
| rs762560330 | 14:74,824,039 | C/T | — | uncertain significance |
| rs768205903 | 14:74,824,040 | G/A | — | uncertain significance |
| rs570368510 | 14:74,824,066 | C/T | — | uncertain significance |
| rs199599167 | 14:74,824,126 | G/A | — | likely benign |
| rs140227220 | 14:74,824,304 | T/C | — | uncertain significance |
| rs746733172 | 14:74,824,342 | T/G | — | uncertain significance |
| rs145081542 | 14:74,824,378 | C/T | — | uncertain significance |
| rs143185421 | 14:74,824,411 | A/G | — | uncertain significance |
| rs1283256009 | 14:74,824,417 | G/A | — | uncertain significance |
| rs779953147 | 14:74,824,427 | T/C | — | uncertain significance |
| rs201579420 | 14:74,824,463 | G/A | — | uncertain significance |
| rs184758289 | 14:74,824,470 | C/T | — | benign |
| rs1024151316 | 14:74,824,471 | G/A | — | uncertain significance |
| rs2506031696 | 14:74,824,497 | G/C | — | uncertain significance |
| rs529639741 | 14:74,824,498 | C/T | — | uncertain significance |
| rs147057914 | 14:74,824,517 | G/A | — | uncertain significance |
| rs1378355642 | 14:74,824,559 | G/A | — | uncertain significance |
| rs138416499 | 14:74,824,664 | C/T | — | uncertain significance |
| rs781550538 | 14:74,824,697 | G/A | — | uncertain significance |
| rs769886367 | 14:74,824,718 | A/G | — | uncertain significance |
| rs370072741 | 14:74,824,763 | G/A | — | uncertain significance |
| rs779382753 | 14:74,824,832 | G/C | — | uncertain significance |
| rs45500395 | 14:74,824,956 | C/A | — | benign |
| rs139241074 | 14:74,824,963 | G/A | — | likely benign |
| rs199857443 | 14:74,825,003 | G/A | — | uncertain significance |
| rs367558909 | 14:74,825,021 | G/A | — | uncertain significance |
| rs372764656 | 14:74,825,168 | C/T | — | uncertain significance |
| rs940877540 | 14:74,825,174 | C/T | — | uncertain significance |
| rs1179501666 | 14:74,825,183 | G/A | — | uncertain significance |
| rs756524090 | 14:74,825,189 | G/A | — | uncertain significance |
| rs745842988 | 14:74,825,213 | A/G | — | uncertain significance |
| rs781768914 | 14:74,825,257 | C/A | — | uncertain significance |
| rs45447993 | 14:74,825,284 | G/A | — | uncertain significance |
| rs1243962348 | 14:74,825,468 | A/G | — | uncertain significance |
| rs2506033082 | 14:74,825,509 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.