CYB561
cytochrome b561
Summary
Predicted to enable transmembrane monodehydroascorbate reductase activity. Predicted to be involved in ascorbate homeostasis. Predicted to be located in chromaffin granule membrane. Predicted to be active in lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3087776 | 17:61,510,278 | C/T | regulatory region variant | — |
| rs184285958 | 17:61,511,791 | G/A | — | uncertain significance |
| rs771391445 | 17:61,511,818 | G/C | — | uncertain significance |
| rs143057314 | 17:61,511,843 | G/A | — | uncertain significance |
| rs754965035 | 17:61,511,869 | T/C | — | uncertain significance |
| rs369317453 | 17:61,511,879 | C/T | — | uncertain significance |
| rs772551964 | 17:61,511,913 | G/A | — | likely benign |
| rs144041303 | 17:61,512,449 | G/A | — | likely benign |
| rs140030064 | 17:61,512,496 | C/T | — | uncertain significance |
| rs149854354 | 17:61,512,546 | C/T | — | uncertain significance |
| rs376683537 | 17:61,512,547 | G/A | — | uncertain significance |
| rs776156464 | 17:61,512,553 | G/A | — | uncertain significance |
| rs766716037 | 17:61,512,571 | C/G | — | uncertain significance |
| rs550908611 | 17:61,512,586 | A/G | — | uncertain significance |
| rs567610276 | 17:61,512,592 | A/G | — | uncertain significance |
| rs761799369 | 17:61,513,111 | C/T | — | uncertain significance |
| rs1599115823 | 17:61,513,117 | C/T | — | uncertain significance |
| rs766550269 | 17:61,513,135 | C/T | — | uncertain significance |
| rs148408441 | 17:61,513,136 | G/A | — | likely benign |
| rs201672820 | 17:61,513,438 | A/G | — | uncertain significance |
| rs772361572 | 17:61,513,454 | C/T | — | pathogenic |
| rs35447397 | 17:61,513,509 | C/T | — | benign |
| rs1437737028 | 17:61,514,778 | C/T | — | pathogenic |
| rs2510661152 | 17:61,514,865 | T/A | — | uncertain significance |
| rs140356224 | 17:61,514,885 | G/A | — | likely benign |
| rs72845004 | 17:61,517,569 | T/C | — | benign |
| rs75195552 | 17:61,524,225 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.