CALN1
calneuron 1
Summary
This gene encodes a protein with high similarity to the calcium-binding proteins of the calmodulin family. The encoded protein contains two EF-hand domains and potential calcium-binding sites. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774961183 | 7:71,252,852 | G/A | — | uncertain significance |
| rs73360079 | 7:71,275,313 | G/T | — | benign |
| rs143545775 | 7:71,275,350 | G/A | — | uncertain significance |
| rs911140713 | 7:71,275,377 | T/C | — | uncertain significance |
| rs761440520 | 7:71,275,431 | T/G | — | uncertain significance |
| rs757746 | 7:71,306,641 | G/T | — | — |
| rs1008516 | 7:71,314,864 | C/T | intron variant | — |
| rs62459050 | 7:71,319,137 | A/G | intron variant | — |
| rs747980961 | 7:71,369,861 | T/C | — | — |
| rs11766496 | 7:71,388,850 | G/C | intron variant | — |
| rs10950290 | 7:71,439,590 | A/T | intron variant | — |
| rs113993793 | 7:71,443,382 | A/G | intron variant | — |
| rs557342382 | 7:71,488,689 | C/T | — | uncertain significance |
| rs2537359985 | 7:71,571,143 | G/C | — | uncertain significance |
| rs144227604 | 7:71,571,191 | C/T | — | benign |
| rs2537360984 | 7:71,571,222 | T/G | — | uncertain significance |
| rs860001 | 7:71,586,211 | A/T | intron variant | — |
| rs73127982 | 7:71,594,519 | T/A | — | — |
| rs4719220 | 7:71,680,703 | G/C | — | — |
| rs73143219 | 7:71,686,609 | C/G | — | — |
| rs76092417 | 7:71,696,113 | T/A | — | — |
| rs34858520 | 7:71,723,883 | A/T | — | — |
| rs7783256 | 7:71,734,574 | G/T | — | — |
| rs35417702 | 7:71,739,916 | C/G | — | — |
| rs35526560 | 7:71,741,232 | C/G | intron variant | — |
| rs1047500611 | 7:71,743,710 | T/C | — | uncertain significance |
| rs376370628 | 7:71,743,764 | C/T | — | uncertain significance |
| rs764214080 | 7:71,743,766 | G/A | — | uncertain significance |
| rs35069269 | 7:71,745,699 | G/T | — | — |
| rs1978102 | 7:71,750,298 | C/T | intron variant | — |
| rs12699131 | 7:71,751,316 | A/G | intron variant | — |
| rs56150095 | 7:71,759,069 | C/G | — | — |
| rs2944823 | 7:71,795,470 | A/C | — | — |
| rs2944821 | 7:71,795,998 | G/A | — | — |
| rs79527984 | 7:71,852,173 | G/A | intron variant | — |
| rs770098230 | 7:71,868,269 | G/A | — | uncertain significance |
| rs541506469 | 7:71,925,860 | G/A | — | — |
| rs191402437 | 7:71,947,914 | A/G | intergenic variant | — |
| rs10280517 | 7:71,966,548 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.