TBCCD1
TBCC domain containing 1
Summary
Involved in several processes, including maintenance of Golgi location; maintenance of centrosome location; and regulation of cell shape. Located in spindle pole centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1714363580 | 3:186,268,981 | G/C | — | uncertain significance |
| rs575140240 | 3:186,269,052 | A/T | — | uncertain significance |
| rs768573493 | 3:186,272,137 | C/T | — | uncertain significance |
| rs61732808 | 3:186,272,156 | C/T | — | benign |
| rs183567505 | 3:186,272,221 | T/C | — | uncertain significance |
| rs771150956 | 3:186,272,295 | G/A | — | uncertain significance |
| rs140309382 | 3:186,272,376 | C/T | — | uncertain significance |
| rs750391893 | 3:186,272,377 | G/A | — | uncertain significance |
| rs373017077 | 3:186,272,509 | T/C | — | uncertain significance |
| rs376119106 | 3:186,272,717 | T/C | — | uncertain significance |
| rs1483264359 | 3:186,272,727 | G/A | — | uncertain significance |
| rs766920672 | 3:186,272,764 | G/T | — | uncertain significance |
| rs751945370 | 3:186,272,765 | C/G | — | uncertain significance |
| rs144614900 | 3:186,274,329 | C/T | — | uncertain significance |
| rs2474527264 | 3:186,274,432 | C/G | — | uncertain significance |
| rs1446430255 | 3:186,274,434 | G/A | — | uncertain significance |
| rs374631235 | 3:186,274,440 | C/T | — | uncertain significance |
| rs988317677 | 3:186,274,443 | G/A | — | uncertain significance |
| rs934365881 | 3:186,274,458 | T/C | — | uncertain significance |
| rs148455051 | 3:186,274,489 | T/G | — | uncertain significance |
| rs776978034 | 3:186,274,530 | T/C | — | likely benign |
| rs765712442 | 3:186,274,540 | C/T | — | uncertain significance |
| rs781424663 | 3:186,276,319 | G/C | — | uncertain significance |
| rs1458678169 | 3:186,276,333 | A/G | — | uncertain significance |
| rs377115116 | 3:186,281,868 | A/G | — | uncertain significance |
| rs201357396 | 3:186,281,869 | T/C | — | likely benign |
| rs763772691 | 3:186,281,904 | G/A | — | uncertain significance |
| rs1438257662 | 3:186,281,967 | C/T | — | uncertain significance |
| rs754017108 | 3:186,281,968 | G/A | — | uncertain significance |
| rs372175818 | 3:186,281,970 | G/A | — | uncertain significance |
| rs531698771 | 3:186,282,024 | T/C | — | uncertain significance |
| rs759456969 | 3:186,282,042 | G/A | — | uncertain significance |
| rs527844882 | 3:186,285,811 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.