SLC35F4
solute carrier family 35 member F4
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs569519209 | 14:58,031,061 | T/C | — | uncertain significance |
| rs2502893299 | 14:58,031,088 | T/C | — | uncertain significance |
| rs201899051 | 14:58,033,205 | G/A | — | uncertain significance |
| rs1336130669 | 14:58,036,599 | G/A | — | uncertain significance |
| rs771358472 | 14:58,038,646 | G/A | — | uncertain significance |
| rs2139706993 | 14:58,038,673 | G/C | — | uncertain significance |
| rs768850457 | 14:58,038,674 | C/T | — | uncertain significance |
| rs2502974707 | 14:58,038,703 | A/G | — | uncertain significance |
| rs201193472 | 14:58,038,735 | T/C | — | uncertain significance |
| rs758805273 | 14:58,038,736 | A/G | — | uncertain significance |
| rs372573599 | 14:58,047,937 | C/T | — | uncertain significance |
| rs760286315 | 14:58,047,958 | G/T | — | uncertain significance |
| rs2503171643 | 14:58,056,010 | T/C | — | uncertain significance |
| rs374207803 | 14:58,056,051 | T/C | — | uncertain significance |
| rs769418504 | 14:58,056,085 | T/A | — | uncertain significance |
| rs1331321847 | 14:58,056,094 | C/T | — | uncertain significance |
| rs773946280 | 14:58,056,150 | A/G | — | uncertain significance |
| rs745535282 | 14:58,056,156 | G/T | — | uncertain significance |
| rs373554837 | 14:58,056,159 | C/G | — | uncertain significance |
| rs756026947 | 14:58,056,211 | G/A | — | uncertain significance |
| rs1414751580 | 14:58,060,713 | T/C | — | uncertain significance |
| rs376265188 | 14:58,060,744 | C/T | — | uncertain significance |
| rs761627655 | 14:58,060,753 | A/G | — | uncertain significance |
| rs2503215618 | 14:58,060,774 | T/C | — | uncertain significance |
| rs12891191 | 14:58,100,283 | G/C | downstream gene variant | — |
| rs1998459 | 14:58,102,523 | A/C | — | — |
| rs10134944 | 14:58,119,196 | C/T | intron variant | — |
| rs1092015 | 14:58,200,725 | A/T | — | — |
| rs8007440 | 14:58,271,405 | T/C | intron variant | — |
| rs74055819 | 14:58,323,245 | A/C | intron variant | — |
| rs973684947 | 14:58,332,531 | C/T | — | uncertain significance |
| rs8013190 | 14:58,355,048 | A/G | intron variant | — |
| rs1335515 | 14:58,385,365 | T/C | intron variant | — |
| rs61583526 | 14:58,393,860 | G/T | — | — |
| rs808225 | 14:58,397,916 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.