SEC14L5
SEC14 like lipid binding 5
Summary
Predicted to be located in mitochondrial intermembrane space. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368031218 | 16:5,009,353 | G/A | — | uncertain significance |
| rs200519895 | 16:5,009,361 | A/G | — | uncertain significance |
| rs80242938 | 16:5,014,069 | A/G | upstream gene variant | — |
| rs11647250 | 16:5,024,530 | C/A | — | — |
| rs1377086706 | 16:5,037,648 | G/A | — | uncertain significance |
| rs751859099 | 16:5,038,150 | A/T | — | uncertain significance |
| rs755837507 | 16:5,038,157 | G/C | — | uncertain significance |
| rs1020959225 | 16:5,038,198 | T/A | — | uncertain significance |
| rs748598785 | 16:5,038,207 | A/G | — | uncertain significance |
| rs1299849452 | 16:5,038,213 | C/T | — | uncertain significance |
| rs201707028 | 16:5,038,232 | A/G | — | uncertain significance |
| rs770336479 | 16:5,038,253 | T/C | — | uncertain significance |
| rs2505672992 | 16:5,040,891 | A/G | — | uncertain significance |
| rs748965438 | 16:5,041,900 | C/T | — | uncertain significance |
| rs369915599 | 16:5,041,920 | G/A | — | uncertain significance |
| rs748149560 | 16:5,041,938 | C/T | — | uncertain significance |
| rs202152916 | 16:5,041,954 | C/T | — | uncertain significance |
| rs777758561 | 16:5,042,017 | C/T | — | uncertain significance |
| rs756805567 | 16:5,042,022 | A/G | — | likely benign |
| rs373411839 | 16:5,042,023 | G/A | — | uncertain significance |
| rs542707406 | 16:5,046,353 | C/G | — | uncertain significance |
| rs201829301 | 16:5,046,364 | C/G | — | uncertain significance |
| rs529226575 | 16:5,046,430 | G/A | — | uncertain significance |
| rs778316449 | 16:5,046,880 | C/T | — | uncertain significance |
| rs367554709 | 16:5,046,896 | A/G | — | likely benign |
| rs199609540 | 16:5,046,919 | C/T | — | uncertain significance |
| rs955243183 | 16:5,046,920 | G/A | — | uncertain significance |
| rs2505683375 | 16:5,046,927 | G/T | — | uncertain significance |
| rs200586557 | 16:5,046,931 | C/T | — | likely benign |
| rs776726374 | 16:5,046,932 | G/A | — | uncertain significance |
| rs776108374 | 16:5,050,704 | G/C | — | uncertain significance |
| rs752914088 | 16:5,050,736 | C/G | — | uncertain significance |
| rs771138868 | 16:5,050,865 | G/C | — | uncertain significance |
| rs776944562 | 16:5,050,887 | G/A | — | uncertain significance |
| rs372393755 | 16:5,050,916 | C/A | — | uncertain significance |
| rs776584035 | 16:5,053,479 | C/T | — | uncertain significance |
| rs761672407 | 16:5,053,484 | G/A | — | uncertain significance |
| rs560880027 | 16:5,055,859 | C/T | — | — |
| rs1346354675 | 16:5,055,921 | C/T | — | uncertain significance |
| rs368032929 | 16:5,055,931 | A/G | — | uncertain significance |
| rs758352257 | 16:5,056,035 | G/T | — | uncertain significance |
| rs780755533 | 16:5,057,395 | A/G | — | uncertain significance |
| rs759374397 | 16:5,057,435 | A/G | — | uncertain significance |
| rs1389809861 | 16:5,058,549 | C/T | — | uncertain significance |
| rs756653747 | 16:5,058,575 | A/G | — | uncertain significance |
| rs765138326 | 16:5,058,634 | G/T | — | uncertain significance |
| rs372747051 | 16:5,061,112 | G/A | — | uncertain significance |
| rs1955795757 | 16:5,061,127 | A/G | — | uncertain significance |
| rs747175243 | 16:5,061,183 | G/A | — | uncertain significance |
| rs781330982 | 16:5,061,252 | G/A | — | uncertain significance |
| rs756391069 | 16:5,061,258 | G/A | — | uncertain significance |
| rs1446167242 | 16:5,061,269 | C/G | — | uncertain significance |
| rs553243910 | 16:5,061,294 | G/T | — | — |
| rs373201837 | 16:5,064,912 | G/A | — | uncertain significance |
| rs374042929 | 16:5,064,931 | C/T | — | uncertain significance |
| rs202181394 | 16:5,064,943 | C/G | — | uncertain significance |
| rs770585482 | 16:5,064,964 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.