TC2N
tandem C2 domains, nuclear
Summary
Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61237505 | 14:92,245,983 | G/C | downstream gene variant | — |
| rs200352735 | 14:92,249,488 | G/C | — | uncertain significance |
| rs1302190235 | 14:92,249,500 | T/C | — | uncertain significance |
| rs766550828 | 14:92,249,548 | T/C | — | uncertain significance |
| rs141598484 | 14:92,251,579 | C/A | — | uncertain significance |
| rs201731267 | 14:92,251,589 | G/A | — | uncertain significance |
| rs759603073 | 14:92,251,609 | C/A | — | uncertain significance |
| rs769904377 | 14:92,258,719 | T/C | — | uncertain significance |
| rs2542540795 | 14:92,258,811 | G/A | — | uncertain significance |
| rs756200562 | 14:92,258,883 | G/A | — | uncertain significance |
| rs572770511 | 14:92,264,130 | T/C | — | uncertain significance |
| rs199769186 | 14:92,264,680 | T/G | — | uncertain significance |
| rs773399002 | 14:92,265,375 | A/T | — | uncertain significance |
| rs1243490404 | 14:92,266,677 | C/A | — | uncertain significance |
| rs1486027340 | 14:92,266,678 | C/A | — | uncertain significance |
| rs57035593 | 14:92,268,096 | C/A | — | — |
| rs10498631 | 14:92,268,531 | C/T | intron variant | — |
| rs779174077 | 14:92,268,639 | C/T | — | uncertain significance |
| rs143829621 | 14:92,268,640 | G/A | — | uncertain significance |
| rs536300405 | 14:92,268,642 | C/T | — | uncertain significance |
| rs536097108 | 14:92,268,669 | T/C | — | uncertain significance |
| rs1251270204 | 14:92,268,673 | T/C | — | uncertain significance |
| rs142964113 | 14:92,268,703 | G/C | — | uncertain significance |
| rs2542577780 | 14:92,268,708 | T/C | — | uncertain significance |
| rs920354679 | 14:92,278,683 | T/A | — | uncertain significance |
| rs150531793 | 14:92,278,757 | G/A | — | uncertain significance |
| rs147433751 | 14:92,278,835 | A/G | — | uncertain significance |
| rs758273122 | 14:92,278,889 | A/G | — | uncertain significance |
| rs61990092 | 14:92,289,301 | C/T | intron variant | — |
| rs58763793 | 14:92,297,571 | C/T | intron variant | — |
| rs58204830 | 14:92,302,972 | G/A | regulatory region variant | — |
| rs12590263 | 14:92,318,498 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.