TENT4A
terminal nucleotidyltransferase 4A
Summary
The protein encoded by this gene is a DNA polymerase that is likely involved in DNA repair. In addition, the encoded protein may be required for sister chromatid adhesion. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jan 2010]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs274668 | 5:6,711,630 | C/T | upstream gene variant | — |
| rs34681760 | 5:6,712,834 | T/C | regulatory region variant | — |
| rs274701 | 5:6,728,707 | C/A | intron variant | — |
| rs377710076 | 5:6,738,823 | G/T | — | uncertain significance |
| rs143476341 | 5:6,739,877 | A/C | — | uncertain significance |
| rs768737746 | 5:6,739,879 | C/T | — | uncertain significance |
| rs62349049 | 5:6,739,924 | G/A | — | uncertain significance |
| rs765306287 | 5:6,742,645 | G/A | — | uncertain significance |
| rs201308363 | 5:6,742,675 | G/A | — | uncertain significance |
| rs577392827 | 5:6,746,179 | C/G | — | — |
| rs1742090083 | 5:6,746,340 | T/C | — | uncertain significance |
| rs557259475 | 5:6,748,609 | A/G | — | uncertain significance |
| rs1347883091 | 5:6,748,667 | C/T | — | uncertain significance |
| rs1363683837 | 5:6,748,696 | G/A | — | uncertain significance |
| rs274680 | 5:6,749,085 | T/G | intron variant | — |
| rs28381415 | 5:6,750,483 | A/G | — | uncertain significance |
| rs141863278 | 5:6,750,522 | A/G | — | uncertain significance |
| rs149890591 | 5:6,751,207 | C/T | — | uncertain significance |
| rs1029384328 | 5:6,753,073 | G/A | — | uncertain significance |
| rs150204125 | 5:6,753,095 | C/T | — | uncertain significance |
| rs371319991 | 5:6,753,103 | C/G | — | uncertain significance |
| rs757204868 | 5:6,753,110 | C/T | — | uncertain significance |
| rs143141039 | 5:6,753,122 | C/T | — | uncertain significance |
| rs773607777 | 5:6,753,128 | C/T | — | uncertain significance |
| rs274677 | 5:6,754,402 | T/G | — | — |
| rs751079673 | 5:6,754,873 | G/A | — | uncertain significance |
| rs779223223 | 5:6,754,903 | G/A | — | likely benign |
| rs780357525 | 5:6,754,915 | G/A | — | uncertain significance |
| rs762098149 | 5:6,754,921 | G/T | — | uncertain significance |
| rs201107006 | 5:6,754,925 | A/G | — | uncertain significance |
| rs374819377 | 5:6,755,003 | G/A | — | uncertain significance |
| rs1364142323 | 5:6,755,054 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.