SLC16A10
solute carrier family 16 member 10
Summary
SLC16A10 is a member of a family of plasma membrane amino acid transporters that mediate the Na(+)-independent transport of aromatic amino acids across the plasma membrane.[supplied by OMIM, Apr 2004]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1445672116 | 6:111,408,995 | A/C | — | uncertain significance |
| rs1353545370 | 6:111,408,998 | A/C | — | uncertain significance |
| rs1328040449 | 6:111,409,001 | G/A | — | uncertain significance |
| rs1173708220 | 6:111,409,059 | C/T | — | uncertain significance |
| rs775150850 | 6:111,409,203 | C/T | — | uncertain significance |
| rs145655903 | 6:111,409,207 | G/A | — | likely benign |
| rs1204183849 | 6:111,409,269 | A/G | — | uncertain significance |
| rs147581822 | 6:111,409,271 | G/A | — | uncertain significance |
| rs1227546144 | 6:111,409,283 | A/T | — | uncertain significance |
| rs9400467 | 6:111,424,015 | C/T | intron variant | — |
| rs9400468 | 6:111,459,969 | C/G | — | — |
| rs6942055 | 6:111,462,757 | T/A | — | — |
| rs1361425 | 6:111,472,243 | A/T | intron variant | — |
| rs241768 | 6:111,492,119 | T/C | intron variant | — |
| rs541891646 | 6:111,493,979 | G/A | — | uncertain significance |
| rs1772610217 | 6:111,493,991 | T/C | — | uncertain significance |
| rs1188410453 | 6:111,494,005 | G/C | — | uncertain significance |
| rs150478295 | 6:111,498,488 | T/C | — | benign |
| rs138486397 | 6:111,498,505 | C/G | — | uncertain significance |
| rs2482388041 | 6:111,498,570 | T/A | — | uncertain significance |
| rs142734633 | 6:111,498,664 | G/C | — | benign |
| rs762586820 | 6:111,498,725 | G/A | — | likely benign |
| rs531084635 | 6:111,498,734 | C/T | — | uncertain significance |
| rs9647629 | 6:111,501,484 | C/T | intron variant | — |
| rs1216019 | 6:111,503,194 | T/G | — | — |
| rs354530 | 6:111,504,489 | T/G | regulatory region variant | — |
| rs433703 | 6:111,512,622 | C/G | — | — |
| rs354540 | 6:111,517,030 | A/G | intron variant | — |
| rs354538 | 6:111,518,066 | G/T | — | — |
| rs1215848 | 6:111,525,536 | T/A | intron variant | — |
| rs761652083 | 6:111,527,808 | A/G | — | uncertain significance |
| rs750713853 | 6:111,527,895 | G/A | — | uncertain significance |
| rs1234598 | 6:111,529,453 | A/T | intron variant | — |
| rs354543 | 6:111,530,253 | G/C | — | — |
| rs201626230 | 6:111,540,032 | T/G | — | uncertain significance |
| rs1583369614 | 6:111,540,041 | C/T | — | likely benign |
| rs148659008 | 6:111,540,044 | A/C | — | uncertain significance |
| rs1770832764 | 6:111,540,087 | T/C | — | uncertain significance |
| rs374926181 | 6:111,540,104 | A/C | — | uncertain significance |
| rs1770835124 | 6:111,540,177 | T/A | — | uncertain significance |
| rs142185010 | 6:111,540,189 | T/C | — | uncertain significance |
| rs375453220 | 6:111,543,299 | C/T | — | uncertain significance |
| rs560761254 | 6:111,543,344 | G/C | — | uncertain significance |
| rs761444142 | 6:111,543,381 | C/G | — | uncertain significance |
| rs762400362 | 6:111,543,385 | C/G | — | uncertain significance |
| rs14399 | 6:111,543,944 | C/A | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.