SLC16A8
solute carrier family 16 member 8
Summary
SLC16A8 is a member of a family of proton-coupled monocarboxylate transporters that mediate lactate transport across cell membranes (Yoon et al., 1999 [PubMed 10493836]).[supplied by OMIM, Apr 2010]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs187455529 | 22:38,474,406 | C/T | — | benign |
| rs750862590 | 22:38,474,407 | G/A | — | likely benign |
| rs546955144 | 22:38,474,412 | C/G | — | uncertain significance |
| rs371969955 | 22:38,474,420 | G/A | — | uncertain significance |
| rs745707368 | 22:38,474,432 | A/G | — | likely benign |
| rs747034934 | 22:38,474,448 | G/A | — | uncertain significance |
| rs377373294 | 22:38,474,461 | G/T | — | uncertain significance |
| rs759948243 | 22:38,474,562 | C/T | — | uncertain significance |
| rs761416594 | 22:38,474,585 | G/A | — | uncertain significance |
| rs751454907 | 22:38,474,604 | G/A | — | uncertain significance |
| rs2517758385 | 22:38,474,676 | T/G | — | uncertain significance |
| rs2517758441 | 22:38,474,706 | G/C | — | uncertain significance |
| rs572012866 | 22:38,474,709 | G/A | — | uncertain significance |
| rs8135665 | 22:38,476,276 | C/T | downstream gene variant | not provided |
| rs1440842328 | 22:38,476,856 | G/A | — | uncertain significance |
| rs908631066 | 22:38,476,868 | G/A | — | uncertain significance |
| rs765385127 | 22:38,476,886 | C/G | — | likely benign |
| rs2085905923 | 22:38,476,975 | T/A | — | uncertain significance |
| rs960916355 | 22:38,477,009 | G/A | — | uncertain significance |
| rs2085908033 | 22:38,477,051 | G/A | — | uncertain significance |
| rs773042604 | 22:38,477,098 | C/T | — | uncertain significance |
| rs1304241343 | 22:38,477,131 | G/T | — | uncertain significance |
| rs754590943 | 22:38,477,153 | C/G | — | uncertain significance |
| rs2085910920 | 22:38,477,161 | A/G | — | uncertain significance |
| rs770955283 | 22:38,477,180 | C/T | — | uncertain significance |
| rs201896042 | 22:38,477,188 | G/A | — | uncertain significance |
| rs781336159 | 22:38,477,276 | C/T | — | uncertain significance |
| rs763842724 | 22:38,477,344 | G/A | — | uncertain significance |
| rs1172607238 | 22:38,477,365 | A/G | — | likely benign |
| rs2517761355 | 22:38,477,390 | C/T | — | uncertain significance |
| rs954191766 | 22:38,477,405 | C/T | — | uncertain significance |
| rs2517761688 | 22:38,477,548 | T/A | — | uncertain significance |
| rs2517761726 | 22:38,477,569 | G/A | — | uncertain significance |
| rs2085919201 | 22:38,477,620 | C/T | — | uncertain significance |
| rs2085919317 | 22:38,477,623 | C/T | — | uncertain significance |
| rs773630609 | 22:38,477,649 | G/C | — | uncertain significance |
| rs2517761907 | 22:38,477,667 | G/T | — | uncertain significance |
| rs2517761930 | 22:38,477,674 | G/C | — | uncertain significance |
| rs1348070753 | 22:38,477,675 | C/G | — | uncertain significance |
| rs2145901003 | 22:38,478,669 | G/A | — | uncertain significance |
| rs188395735 | 22:38,478,679 | G/A | — | benign |
| rs780287223 | 22:38,478,718 | T/C | — | uncertain significance |
| rs752526414 | 22:38,478,724 | C/T | — | uncertain significance |
| rs371655574 | 22:38,478,726 | G/T | — | uncertain significance |
| rs1332378841 | 22:38,478,727 | C/T | — | uncertain significance |
| rs1347118760 | 22:38,478,766 | C/A | — | uncertain significance |
| rs2085940273 | 22:38,478,813 | C/T | — | uncertain significance |
| rs1257501144 | 22:38,478,837 | C/T | — | uncertain significance |
| rs766836633 | 22:38,478,841 | C/T | — | uncertain significance |
| rs936491448 | 22:38,478,861 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.