NUDT19
nudix hydrolase 19
Summary
Predicted to enable magnesium ion binding activity. Predicted to be involved in acyl-CoA metabolic process and coenzyme A catabolic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3892630 | 19:33,181,484 | C/T | regulatory region variant | — |
| rs1303303323 | 19:33,182,874 | G/A | — | uncertain significance |
| rs374445377 | 19:33,182,882 | C/T | — | uncertain significance |
| rs891997083 | 19:33,182,928 | C/A | — | uncertain significance |
| rs1021424199 | 19:33,182,930 | G/C | — | uncertain significance |
| rs2513262977 | 19:33,182,934 | G/A | — | uncertain significance |
| rs1439318364 | 19:33,182,997 | T/A | — | uncertain significance |
| rs1240508545 | 19:33,183,006 | T/G | — | uncertain significance |
| rs2513263146 | 19:33,183,011 | C/T | — | uncertain significance |
| rs765418100 | 19:33,183,077 | G/A | — | uncertain significance |
| rs1968192725 | 19:33,183,081 | G/C | — | uncertain significance |
| rs1568430528 | 19:33,183,102 | T/G | — | uncertain significance |
| rs776594450 | 19:33,183,107 | G/A | — | uncertain significance |
| rs764181029 | 19:33,183,108 | C/A | — | uncertain significance |
| rs770716224 | 19:33,183,129 | G/C | — | uncertain significance |
| rs556441813 | 19:33,183,134 | G/A | — | uncertain significance |
| rs75564582 | 19:33,183,159 | G/C | — | uncertain significance |
| rs765753461 | 19:33,183,190 | T/G | — | uncertain significance |
| rs757904981 | 19:33,183,200 | A/G | — | likely benign |
| rs763532363 | 19:33,183,203 | G/A | — | uncertain significance |
| rs756906232 | 19:33,183,213 | G/C | — | likely benign |
| rs749181505 | 19:33,183,227 | G/A | — | uncertain significance |
| rs756676136 | 19:33,183,251 | G/C | — | uncertain significance |
| rs374306347 | 19:33,183,255 | G/A | — | uncertain significance |
| rs2513263982 | 19:33,183,309 | C/T | — | uncertain significance |
| rs749687457 | 19:33,183,320 | C/G | — | uncertain significance |
| rs2513264073 | 19:33,183,326 | C/T | — | uncertain significance |
| rs775112575 | 19:33,183,368 | C/T | — | uncertain significance |
| rs751434606 | 19:33,183,371 | G/A | — | uncertain significance |
| rs2145353323 | 19:33,183,372 | A/C | — | likely benign |
| rs748483677 | 19:33,183,393 | G/A | — | uncertain significance |
| rs751450486 | 19:33,183,428 | A/G | — | uncertain significance |
| rs752916743 | 19:33,183,486 | G/T | — | uncertain significance |
| rs750887008 | 19:33,183,495 | G/A | — | uncertain significance |
| rs760646276 | 19:33,183,509 | G/T | — | uncertain significance |
| rs527921465 | 19:33,183,534 | A/G | — | uncertain significance |
| rs959229017 | 19:33,183,554 | G/A | — | uncertain significance |
| rs147910567 | 19:33,183,584 | A/G | — | benign |
| rs35709439 | 19:33,190,263 | C/T | intron variant | — |
| rs12975429 | 19:33,199,227 | G/A | intron variant | — |
| rs369783028 | 19:33,200,127 | T/C | — | uncertain significance |
| rs762526101 | 19:33,200,159 | C/G | — | uncertain significance |
| rs1568435207 | 19:33,200,188 | C/T | — | uncertain significance |
| rs200929233 | 19:33,200,223 | C/T | — | uncertain significance |
| rs184454636 | 19:33,200,254 | C/T | — | uncertain significance |
| rs371226805 | 19:33,200,275 | A/T | — | uncertain significance |
| rs1414479197 | 19:33,200,277 | G/A | — | uncertain significance |
| rs772935446 | 19:33,200,287 | A/C | — | uncertain significance |
| rs371717452 | 19:33,202,756 | C/T | — | uncertain significance |
| rs746589893 | 19:33,202,757 | G/A | — | uncertain significance |
| rs371407959 | 19:33,202,775 | G/A | — | uncertain significance |
| rs77865788 | 19:33,202,795 | G/C | — | uncertain significance |
| rs753294436 | 19:33,202,822 | G/A | — | uncertain significance |
| rs1568435851 | 19:33,202,831 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.