HEATR4
HEAT repeat containing 4
Summary
Predicted to enable oxidoreductase activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants98 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2504131634 | 14:73,945,316 | G/A | — | likely benign |
| rs139188683 | 14:73,945,346 | A/G | — | uncertain significance |
| rs150958075 | 14:73,945,399 | G/C | — | uncertain significance |
| rs141489673 | 14:73,945,474 | C/T | — | likely benign |
| rs1012161417 | 14:73,945,524 | A/T | — | uncertain significance |
| rs368885398 | 14:73,961,986 | T/C | — | uncertain significance |
| rs143634597 | 14:73,962,004 | G/A | — | uncertain significance |
| rs769705232 | 14:73,962,022 | C/G | — | uncertain significance |
| rs562665737 | 14:73,962,028 | C/T | — | likely benign |
| rs374999620 | 14:73,962,036 | A/G | — | uncertain significance |
| rs143275602 | 14:73,963,319 | C/G | — | uncertain significance |
| rs202004334 | 14:73,963,340 | C/T | — | uncertain significance |
| rs148329758 | 14:73,963,355 | T/C | — | uncertain significance |
| rs746303750 | 14:73,964,869 | C/T | — | uncertain significance |
| rs139754765 | 14:73,964,893 | C/T | — | uncertain significance |
| rs370727396 | 14:73,964,902 | A/G | — | uncertain significance |
| rs764956991 | 14:73,964,916 | C/T | — | likely benign |
| rs777656399 | 14:73,964,925 | T/A | — | uncertain significance |
| rs543425089 | 14:73,964,949 | C/T | — | uncertain significance |
| rs1194411570 | 14:73,964,971 | C/T | — | uncertain significance |
| rs529234872 | 14:73,965,012 | G/A | — | uncertain significance |
| rs2504180666 | 14:73,965,017 | C/G | — | uncertain significance |
| rs751535322 | 14:73,965,777 | C/T | — | uncertain significance |
| rs768238517 | 14:73,967,304 | G/A | — | uncertain significance |
| rs371493329 | 14:73,967,354 | T/C | — | uncertain significance |
| rs762917216 | 14:73,969,609 | C/T | — | uncertain significance |
| rs2504194149 | 14:73,969,651 | C/T | — | uncertain significance |
| rs372061895 | 14:73,969,688 | C/T | — | uncertain significance |
| rs781088389 | 14:73,969,707 | T/C | — | uncertain significance |
| rs745827012 | 14:73,969,711 | T/C | — | uncertain significance |
| rs2041073 | 14:73,972,535 | T/C | intron variant | — |
| rs138786560 | 14:73,973,175 | C/A | — | uncertain significance |
| rs375929384 | 14:73,973,186 | A/T | — | uncertain significance |
| rs375723728 | 14:73,973,194 | G/A | — | uncertain significance |
| rs370313641 | 14:73,973,218 | T/A | — | uncertain significance |
| rs372980757 | 14:73,973,220 | C/T | — | uncertain significance |
| rs1448105262 | 14:73,973,257 | G/C | — | uncertain significance |
| rs11159021 | 14:73,974,531 | T/C | intron variant | — |
| rs1341500108 | 14:73,974,845 | T/C | — | likely benign |
| rs199865768 | 14:73,974,951 | C/T | — | uncertain significance |
| rs146144273 | 14:73,976,046 | G/C | — | uncertain significance |
| rs1192737602 | 14:73,976,094 | C/A | — | uncertain significance |
| rs1317181908 | 14:73,976,133 | C/G | — | uncertain significance |
| rs150885411 | 14:73,976,156 | G/A | — | uncertain significance |
| rs8018967 | 14:73,976,934 | T/C | intron variant | — |
| rs139427381 | 14:73,978,743 | G/A | — | uncertain significance |
| rs369061780 | 14:73,978,767 | T/C | — | uncertain significance |
| rs777866454 | 14:73,978,785 | G/A | — | uncertain significance |
| rs2504230534 | 14:73,978,790 | T/C | — | uncertain significance |
| rs2504230650 | 14:73,978,802 | T/A | — | uncertain significance |
| rs150212644 | 14:73,980,746 | G/T | — | uncertain significance |
| rs1887435546 | 14:73,980,747 | C/A | — | uncertain significance |
| rs1335230964 | 14:73,980,767 | A/C | — | uncertain significance |
| rs142163355 | 14:73,980,790 | C/G | — | uncertain significance |
| rs771534359 | 14:73,980,825 | T/G | — | uncertain significance |
| rs746934893 | 14:73,980,905 | G/C | — | uncertain significance |
| rs184973348 | 14:73,985,827 | G/C | — | uncertain significance |
| rs116927336 | 14:73,987,566 | C/G | — | uncertain significance |
| rs1300933493 | 14:73,987,571 | G/C | — | uncertain significance |
| rs774589942 | 14:73,987,594 | T/C | — | uncertain significance |
| rs1887936863 | 14:73,987,642 | G/T | — | likely benign |
| rs2504261951 | 14:73,987,649 | G/A | — | uncertain significance |
| rs748298379 | 14:73,987,687 | C/T | — | uncertain significance |
| rs2504266430 | 14:73,989,021 | G/T | — | uncertain significance |
| rs1346856903 | 14:73,989,096 | C/G | — | uncertain significance |
| rs149734041 | 14:73,989,211 | G/A | — | uncertain significance |
| rs755190660 | 14:73,989,219 | C/T | — | uncertain significance |
| rs2504267727 | 14:73,989,277 | G/A | — | uncertain significance |
| rs2504267745 | 14:73,989,283 | G/A | — | uncertain significance |
| rs79761456 | 14:73,989,373 | G/A | — | uncertain significance |
| rs144060453 | 14:73,989,384 | C/T | — | likely benign |
| rs753869255 | 14:73,989,417 | T/G | — | uncertain significance |
| rs771665931 | 14:73,989,471 | G/T | — | uncertain significance |
| rs759582313 | 14:73,989,522 | C/T | — | likely benign |
| rs149611197 | 14:73,989,608 | C/G | — | likely benign |
| rs1244370547 | 14:73,989,640 | A/G | — | uncertain significance |
| rs200488186 | 14:73,989,660 | A/G | — | uncertain significance |
| rs764475068 | 14:73,989,681 | C/G | — | uncertain significance |
| rs751814732 | 14:73,989,682 | G/A | — | uncertain significance |
| rs1427060211 | 14:73,989,820 | G/T | — | uncertain significance |
| rs537815197 | 14:73,989,837 | C/T | — | likely benign |
| rs36059280 | 14:73,994,728 | C/A | intron variant | — |
| rs55705802 | 14:73,995,075 | G/A | — | — |
| rs191093499 | 14:73,997,881 | C/A | downstream gene variant | — |
| rs58231493 | 14:74,032,122 | C/G | — | — |
| rs138127491 | 14:74,043,748 | C/T | downstream gene variant | — |
| rs74061172 | 14:74,044,251 | T/C | regulatory region variant | — |
| rs116746541 | 14:74,049,636 | T/G | intergenic variant | — |
| rs7159760 | 14:74,056,148 | C/T | upstream gene variant | — |
| rs113831731 | 14:74,064,853 | G/A | downstream gene variant | — |
| rs61988863 | 14:74,066,270 | G/A | downstream gene variant | — |
| rs61988864 | 14:74,067,702 | A/G | downstream gene variant | — |
| rs111511359 | 14:74,077,186 | G/T | upstream gene variant | — |
| rs55826256 | 14:74,079,209 | G/C | regulatory region variant | — |
| rs554110712 | 14:74,086,776 | C/A | — | — |
| rs62004879 | 14:74,094,274 | C/T | upstream gene variant | — |
| rs4903129 | 14:74,095,713 | A/G | — | — |
| rs72719670 | 14:74,096,048 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.