NUCB1
nucleobindin 1
Summary
This gene encodes a member of a small calcium-binding EF-hand protein family. The encoded protein is thought to have a key role in Golgi calcium homeostasis and Ca(2+)-regulated signal transduction events. [provided by RefSeq, Jun 2010]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs149579121 | 19:49,404,079 | C/T | — | uncertain significance |
| rs1341041842 | 19:49,404,127 | T/C | — | uncertain significance |
| rs565603581 | 19:49,404,147 | G/C | — | uncertain significance |
| rs138618172 | 19:49,406,665 | G/A | upstream gene variant | — |
| rs939666852 | 19:49,407,614 | T/G | — | uncertain significance |
| rs201423625 | 19:49,407,626 | G/A | — | uncertain significance |
| rs897045509 | 19:49,409,037 | T/A | — | uncertain significance |
| rs754804979 | 19:49,409,053 | T/A | — | uncertain significance |
| rs150499093 | 19:49,409,067 | G/T | — | uncertain significance |
| rs149685717 | 19:49,409,095 | G/A | — | uncertain significance |
| rs11667423 | 19:49,412,509 | T/G | — | — |
| rs201726333 | 19:49,414,442 | T/C | — | uncertain significance |
| rs767591310 | 19:49,416,284 | C/T | — | uncertain significance |
| rs143826495 | 19:49,416,349 | C/T | — | uncertain significance |
| rs767608317 | 19:49,416,350 | G/A | — | uncertain significance |
| rs753001033 | 19:49,416,353 | G/A | — | uncertain significance |
| rs768095731 | 19:49,416,419 | G/A | — | uncertain significance |
| rs746986744 | 19:49,416,753 | A/C | — | uncertain significance |
| rs181852425 | 19:49,416,813 | T/C | — | uncertain significance |
| rs150201926 | 19:49,421,985 | A/G | — | uncertain significance |
| rs375263053 | 19:49,422,308 | A/C | — | uncertain significance |
| rs760463469 | 19:49,422,343 | G/T | — | uncertain significance |
| rs757681738 | 19:49,422,492 | C/G | — | uncertain significance |
| rs142089243 | 19:49,422,507 | G/T | — | uncertain significance |
| rs776437305 | 19:49,424,454 | G/A | — | uncertain significance |
| rs370804111 | 19:49,424,477 | C/T | — | uncertain significance |
| rs148698634 | 19:49,424,508 | G/A | — | uncertain significance |
| rs1388944281 | 19:49,424,528 | G/A | — | uncertain significance |
| rs773635496 | 19:49,424,534 | G/C | — | uncertain significance |
| rs778971270 | 19:49,425,583 | C/G | — | uncertain significance |
| rs2514385154 | 19:49,425,584 | C/T | — | uncertain significance |
| rs758852318 | 19:49,425,596 | C/T | — | uncertain significance |
| rs762055911 | 19:49,425,655 | G/A | — | uncertain significance |
| rs139369639 | 19:49,425,664 | G/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.