SLC38A10
solute carrier family 38 member 10
Summary
Predicted to enable L-amino acid transmembrane transporter activity. Predicted to be involved in amino acid transmembrane transport. Predicted to act upstream of or within bone development. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2659005 | 17:79,218,714 | C/G | — | — |
| rs760367168 | 17:79,219,403 | G/A | — | uncertain significance |
| rs376896275 | 17:79,219,436 | G/A | — | uncertain significance |
| rs200407214 | 17:79,219,651 | A/G | — | likely benign |
| rs1479389389 | 17:79,219,797 | C/G | — | uncertain significance |
| rs368621227 | 17:79,219,900 | G/A | — | likely benign |
| rs147849926 | 17:79,219,937 | T/C | — | likely benign |
| rs2512123858 | 17:79,220,003 | T/C | — | likely benign |
| rs775204418 | 17:79,220,098 | C/T | — | likely benign |
| rs372430209 | 17:79,220,126 | C/T | — | uncertain significance |
| rs2725405 | 17:79,220,224 | G/T | missense variant | — |
| rs116990218 | 17:79,225,040 | C/T | — | likely benign |
| rs200011449 | 17:79,225,239 | G/A | — | likely benign |
| rs752422072 | 17:79,225,310 | G/A | — | uncertain significance |
| rs770439555 | 17:79,225,325 | G/A | — | likely benign |
| rs61740870 | 17:79,225,328 | C/T | — | uncertain significance |
| rs781063838 | 17:79,225,348 | G/A | — | likely benign |
| rs2062914461 | 17:79,225,364 | A/C | — | uncertain significance |
| rs1379604657 | 17:79,225,373 | C/A | — | uncertain significance |
| rs140451634 | 17:79,226,042 | C/A | — | uncertain significance |
| rs61740860 | 17:79,226,048 | G/A | — | likely benign |
| rs199508563 | 17:79,226,051 | G/A | — | uncertain significance |
| rs780284908 | 17:79,226,058 | C/T | — | uncertain significance |
| rs1420622940 | 17:79,226,091 | C/T | — | uncertain significance |
| rs781308491 | 17:79,226,130 | G/A | — | uncertain significance |
| rs2512144398 | 17:79,226,132 | A/G | — | uncertain significance |
| rs1299070033 | 17:79,226,184 | G/C | — | uncertain significance |
| rs1445910963 | 17:79,226,190 | C/G | — | uncertain significance |
| rs779778217 | 17:79,226,262 | T/A | — | uncertain significance |
| rs199990595 | 17:79,226,285 | G/A | — | uncertain significance |
| rs1410421530 | 17:79,226,318 | G/C | — | uncertain significance |
| rs769255151 | 17:79,226,346 | G/A | — | uncertain significance |
| rs772492283 | 17:79,226,360 | G/A | — | likely benign |
| rs777202842 | 17:79,226,454 | G/A | — | uncertain significance |
| rs373504148 | 17:79,226,463 | C/T | — | uncertain significance |
| rs138614314 | 17:79,226,876 | G/C | — | uncertain significance |
| rs781723291 | 17:79,226,884 | C/T | — | uncertain significance |
| rs2512147498 | 17:79,226,977 | C/T | — | likely benign |
| rs111329381 | 17:79,226,986 | G/A | — | uncertain significance |
| rs372590267 | 17:79,227,004 | C/T | — | uncertain significance |
| rs764911435 | 17:79,227,005 | G/A | — | uncertain significance |
| rs910035485 | 17:79,234,044 | G/A | — | uncertain significance |
| rs151281009 | 17:79,234,074 | C/T | — | uncertain significance |
| rs774049428 | 17:79,234,086 | G/A | — | uncertain significance |
| rs34228248 | 17:79,234,180 | A/G | — | benign |
| rs7224668 | 17:79,235,788 | T/C | intron variant | — |
| rs376849786 | 17:79,244,725 | G/C | — | uncertain significance |
| rs369477188 | 17:79,244,798 | C/T | — | uncertain significance |
| rs531109499 | 17:79,246,381 | C/T | — | uncertain significance |
| rs200657122 | 17:79,246,390 | G/T | — | uncertain significance |
| rs2512184925 | 17:79,246,412 | A/C | — | uncertain significance |
| rs2512191956 | 17:79,249,788 | G/A | — | uncertain significance |
| rs2063157842 | 17:79,249,797 | G/A | — | uncertain significance |
| rs1247293706 | 17:79,249,804 | T/C | — | uncertain significance |
| rs1202842621 | 17:79,249,816 | T/C | — | uncertain significance |
| rs201350859 | 17:79,249,861 | G/A | — | uncertain significance |
| rs141866759 | 17:79,249,897 | T/C | — | uncertain significance |
| rs2512192759 | 17:79,249,930 | T/C | — | uncertain significance |
| rs747278374 | 17:79,254,472 | T/C | — | uncertain significance |
| rs767217469 | 17:79,254,509 | C/T | — | uncertain significance |
| rs141053452 | 17:79,256,117 | G/A | — | uncertain significance |
| rs138694564 | 17:79,257,223 | G/T | — | uncertain significance |
| rs146237661 | 17:79,257,236 | G/T | — | uncertain significance |
| rs773068694 | 17:79,257,246 | A/C | — | uncertain significance |
| rs749971126 | 17:79,257,262 | C/T | — | uncertain significance |
| rs10445407 | 17:79,261,809 | C/A | intron variant | — |
| rs762191909 | 17:79,263,497 | C/T | — | uncertain significance |
| rs2063296176 | 17:79,263,581 | A/C | — | uncertain significance |
| rs370058411 | 17:79,263,589 | G/A | — | uncertain significance |
| rs752753260 | 17:79,263,599 | C/T | — | uncertain significance |
| rs964645804 | 17:79,268,642 | A/T | — | uncertain significance |
| rs2063336259 | 17:79,268,667 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.