SHTN1
shootin 1
Summary
Enables identical protein binding activity. Involved in positive regulation of neuron migration. Located in cytoplasm and microtubule. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs187127258 | 10:118,659,183 | C/G | intron variant | — |
| rs957321262 | 10:118,661,282 | G/A | — | uncertain significance |
| rs200753974 | 10:118,661,316 | G/A | — | likely benign |
| rs1847748864 | 10:118,661,331 | G/A | — | uncertain significance |
| rs368351085 | 10:118,661,337 | G/A | — | uncertain significance |
| rs200045766 | 10:118,666,162 | C/A | — | uncertain significance |
| rs954569687 | 10:118,666,167 | C/T | — | uncertain significance |
| rs187306103 | 10:118,666,210 | G/T | — | likely benign |
| rs62641722 | 10:118,671,343 | C/T | — | benign |
| rs373191933 | 10:118,674,915 | C/T | — | uncertain significance |
| rs4638225 | 10:118,676,964 | G/A | intron variant | — |
| rs2493064701 | 10:118,687,340 | G/C | — | uncertain significance |
| rs2493071406 | 10:118,689,366 | G/A | — | uncertain significance |
| rs147568150 | 10:118,711,203 | C/G | intron variant | — |
| rs551678925 | 10:118,711,437 | C/T | — | uncertain significance |
| rs895028332 | 10:118,713,600 | C/T | — | uncertain significance |
| rs72833408 | 10:118,723,484 | G/T | — | — |
| rs769962385 | 10:118,764,581 | A/C | — | uncertain significance |
| rs10787738 | 10:118,777,371 | C/T | intron variant | — |
| rs10886022 | 10:118,778,079 | A/G | — | — |
| rs10886032 | 10:118,805,708 | A/C | intron variant | — |
| rs9787575 | 10:118,813,877 | C/T | intron variant | — |
| rs1898349 | 10:118,817,067 | C/A | — | — |
| rs7078160 | 10:118,827,560 | G/A | intron variant | — |
| rs3847479 | 10:118,833,263 | A/G | intron variant | — |
| rs4752028 | 10:118,834,991 | C/T | intron variant | — |
| rs10886040 | 10:118,846,294 | C/G | regulatory region variant | — |
| rs1947798 | 10:118,855,241 | C/G | — | — |
| rs17095681 | 10:118,860,777 | G/T | intron variant | — |
| rs10886043 | 10:118,876,412 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.