SUPV3L1
Suv3 like RNA helicase
Summary
Enables several functions, including double-stranded RNA binding activity; helicase activity; and protein homodimerization activity. Involved in several processes, including mitochondrial RNA 3'-end processing; mitochondrial RNA surveillance; and positive regulation of mitochondrial RNA catabolic process. Located in mitochondrial nucleoid and nucleus. Part of mitochondrial degradosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10998624 | 10:70,939,801 | G/A | regulatory region variant | — |
| rs1842010747 | 10:70,940,060 | C/G | — | uncertain significance |
| rs757576646 | 10:70,940,063 | G/T | — | uncertain significance |
| rs199886131 | 10:70,940,133 | G/A | — | uncertain significance |
| rs376027793 | 10:70,940,146 | G/A | — | likely benign |
| rs373167154 | 10:70,940,174 | T/G | — | uncertain significance |
| rs1345137941 | 10:70,940,208 | G/C | — | uncertain significance |
| rs147077704 | 10:70,940,217 | A/G | — | uncertain significance |
| rs752705209 | 10:70,940,244 | C/T | — | uncertain significance |
| rs201283581 | 10:70,940,264 | G/A | — | uncertain significance |
| rs10998625 | 10:70,941,700 | A/G | intron variant | — |
| rs747352753 | 10:70,946,235 | A/C | — | uncertain significance |
| rs374862991 | 10:70,946,292 | T/C | — | uncertain significance |
| rs568133891 | 10:70,946,300 | G/A | — | likely benign |
| rs141575091 | 10:70,947,421 | T/A | — | uncertain significance |
| rs752162947 | 10:70,947,445 | A/G | — | uncertain significance |
| rs374901378 | 10:70,947,478 | C/T | — | uncertain significance |
| rs1842324977 | 10:70,949,121 | C/A | — | uncertain significance |
| rs1564702520 | 10:70,949,183 | A/G | — | uncertain significance |
| rs1842404753 | 10:70,951,514 | C/G | — | uncertain significance |
| rs200013555 | 10:70,956,792 | A/G | — | uncertain significance |
| rs779243875 | 10:70,956,822 | A/G | — | uncertain significance |
| rs968465097 | 10:70,958,138 | A/G | — | uncertain significance |
| rs376727615 | 10:70,958,198 | G/A | — | uncertain significance |
| rs372218148 | 10:70,958,251 | C/T | — | uncertain significance |
| rs199507911 | 10:70,958,899 | A/G | — | uncertain significance |
| rs148715762 | 10:70,958,934 | A/G | — | uncertain significance |
| rs368918225 | 10:70,960,160 | A/G | — | uncertain significance |
| rs773846894 | 10:70,960,184 | G/A | — | uncertain significance |
| rs1379527145 | 10:70,960,202 | G/C | — | uncertain significance |
| rs2539852229 | 10:70,962,762 | A/G | — | likely benign |
| rs2539863414 | 10:70,967,564 | A/G | — | uncertain significance |
| rs201773412 | 10:70,967,597 | C/T | — | uncertain significance |
| rs141062949 | 10:70,967,610 | A/G | — | uncertain significance |
| rs150112121 | 10:70,967,669 | G/A | — | uncertain significance |
| rs202133775 | 10:70,968,361 | G/A | — | uncertain significance |
| rs200270601 | 10:70,968,382 | A/G | — | uncertain significance |
| rs1226093472 | 10:70,968,402 | C/G | — | uncertain significance |
| rs370048763 | 10:70,968,436 | G/A | — | uncertain significance |
| rs768639246 | 10:70,968,445 | A/G | — | uncertain significance |
| rs758194309 | 10:70,968,529 | C/T | — | uncertain significance |
| rs766861162 | 10:70,968,562 | G/A | — | uncertain significance |
| rs201953351 | 10:70,968,564 | G/A | — | uncertain significance |
| rs200900544 | 10:70,968,613 | C/A | — | uncertain significance |
| rs1454083602 | 10:70,968,685 | A/G | — | uncertain significance |
| rs777532789 | 10:70,968,785 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.