SLC25A48
solute carrier family 25 member 48
Summary
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in mitochondrial inner membrane. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150165884 | 5:134,927,409 | C/A | intron variant | — |
| rs31263 | 5:134,968,962 | G/C | intron variant | — |
| rs577205521 | 5:135,003,262 | C/T | — | — |
| rs144775021 | 5:135,034,270 | A/G | — | — |
| rs781235830 | 5:135,074,531 | G/A | — | — |
| rs187875014 | 5:135,078,097 | C/T | downstream gene variant | — |
| rs567391214 | 5:135,090,593 | G/A | — | — |
| rs181579884 | 5:135,103,300 | C/T | intergenic variant | — |
| rs181701790 | 5:135,149,820 | A/C | intron variant | — |
| rs13178541 | 5:135,164,618 | A/C | downstream gene variant | — |
| rs185839367 | 5:135,168,055 | C/T | upstream gene variant | — |
| rs373533677 | 5:135,186,163 | G/A | — | uncertain significance |
| rs370830017 | 5:135,186,165 | G/A | — | likely benign |
| rs776879348 | 5:135,186,176 | G/T | — | uncertain significance |
| rs78991141 | 5:135,187,551 | C/T | intron variant | — |
| rs746170434 | 5:135,188,288 | G/A | — | uncertain significance |
| rs756415069 | 5:135,188,366 | G/A | — | likely benign |
| rs376094750 | 5:135,188,456 | C/A | — | uncertain significance |
| rs766940846 | 5:135,188,499 | C/G | — | uncertain significance |
| rs4976511 | 5:135,201,164 | C/T | intron variant | — |
| rs534989893 | 5:135,205,138 | G/A | — | — |
| rs200164783 | 5:135,207,148 | A/G | intron variant | — |
| rs7734448 | 5:135,214,677 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.