TATDN2
TatD DNase domain containing 2
Summary
Predicted to enable metal ion binding activity and nuclease activity. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs772726630 | 3:10,290,955 | G/C | — | uncertain significance |
| rs751106344 | 3:10,290,984 | C/T | — | uncertain significance |
| rs139680303 | 3:10,291,053 | G/A | — | uncertain significance |
| rs144351497 | 3:10,291,083 | C/T | — | uncertain significance |
| rs916902564 | 3:10,291,110 | C/T | — | uncertain significance |
| rs761680364 | 3:10,291,156 | C/G | — | uncertain significance |
| rs530905999 | 3:10,291,171 | C/T | — | uncertain significance |
| rs373299416 | 3:10,291,271 | T/G | — | likely benign |
| rs1464804601 | 3:10,301,833 | G/A | — | uncertain significance |
| rs2470287005 | 3:10,301,836 | A/G | — | uncertain significance |
| rs1347591559 | 3:10,301,999 | C/T | — | uncertain significance |
| rs1559460987 | 3:10,302,082 | A/G | — | uncertain significance |
| rs762755485 | 3:10,302,190 | A/G | — | uncertain significance |
| rs368345107 | 3:10,302,218 | A/G | — | likely benign |
| rs772292150 | 3:10,302,338 | A/G | — | uncertain significance |
| rs146692767 | 3:10,311,262 | G/A | intron variant | — |
| rs1183040057 | 3:10,311,900 | C/G | — | uncertain significance |
| rs191162344 | 3:10,311,980 | C/G | — | likely benign |
| rs778153707 | 3:10,312,040 | C/T | — | uncertain significance |
| rs750053141 | 3:10,312,052 | C/T | — | uncertain significance |
| rs758008127 | 3:10,312,059 | C/T | — | uncertain significance |
| rs143575255 | 3:10,312,075 | C/T | — | likely benign |
| rs150695751 | 3:10,312,121 | T/C | — | uncertain significance |
| rs775567522 | 3:10,312,158 | C/T | — | uncertain significance |
| rs762071006 | 3:10,312,175 | T/G | — | likely benign |
| rs1698544623 | 3:10,312,176 | C/T | — | uncertain significance |
| rs765699282 | 3:10,312,181 | G/A | — | uncertain significance |
| rs773658778 | 3:10,312,280 | C/T | — | uncertain significance |
| rs202027258 | 3:10,312,311 | T/C | — | uncertain significance |
| rs1698548052 | 3:10,312,353 | T/C | — | uncertain significance |
| rs750329499 | 3:10,312,571 | C/T | — | uncertain significance |
| rs115984909 | 3:10,312,633 | G/A | — | likely benign |
| rs2287544 | 3:10,316,762 | C/T | intron variant | — |
| rs3774203 | 3:10,317,489 | G/A | intron variant | — |
| rs2470305241 | 3:10,318,112 | C/T | — | uncertain significance |
| rs765079750 | 3:10,318,153 | C/T | — | likely benign |
| rs778424624 | 3:10,319,986 | C/G | — | uncertain significance |
| rs1229635528 | 3:10,320,618 | C/T | — | uncertain significance |
| rs778724431 | 3:10,320,686 | A/G | — | uncertain significance |
| rs1063429 | 3:10,320,968 | T/G | — | — |
| rs4684676 | 3:10,323,108 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.