TRAK1
trafficking kinesin protein 1
Summary
Predicted to enable GABA receptor binding activity and myosin binding activity. Involved in endosome to lysosome transport. Located in early endosome and mitochondrion. Implicated in developmental and epileptic encephalopathy 68. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants224 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1498095 | 3:42,093,422 | T/C | regulatory region variant | — |
| rs757732298 | 3:42,128,829 | A/G | — | uncertain significance |
| rs754091914 | 3:42,132,962 | A/G | — | uncertain significance |
| rs765641177 | 3:42,132,973 | T/G | — | likely benign |
| rs116661356 | 3:42,132,983 | G/A | — | benign |
| rs201790561 | 3:42,132,994 | C/G | — | likely benign |
| rs200776452 | 3:42,133,013 | G/A | — | uncertain significance |
| rs750737796 | 3:42,133,038 | G/A | — | uncertain significance |
| rs148528673 | 3:42,133,045 | C/T | — | likely benign |
| rs773333328 | 3:42,166,916 | G/C | — | uncertain significance |
| rs149366200 | 3:42,166,937 | G/A | — | benign |
| rs374392581 | 3:42,166,940 | A/G | — | likely benign |
| rs61742102 | 3:42,166,943 | C/T | — | benign |
| rs201653558 | 3:42,166,995 | G/A | — | likely benign |
| rs201869432 | 3:42,167,006 | C/T | — | likely benign |
| rs748182696 | 3:42,167,007 | G/A | — | uncertain significance |
| rs1710442494 | 3:42,167,030 | C/G | — | likely benign |
| rs201136046 | 3:42,167,032 | A/G | — | uncertain significance |
| rs774718665 | 3:42,167,092 | C/T | — | uncertain significance |
| rs772587793 | 3:42,167,101 | A/T | — | uncertain significance |
| rs2149140090 | 3:42,167,107 | G/A | — | pathogenic |
| rs763658009 | 3:42,167,113 | A/G | — | likely benign |
| rs199836147 | 3:42,167,122 | T/C | — | benign |
| rs114149261 | 3:42,169,392 | C/A | — | — |
| rs72869936 | 3:42,178,862 | T/A | intron variant | — |
| rs376792946 | 3:42,191,045 | A/G | — | likely benign |
| rs1018509561 | 3:42,191,047 | C/T | — | uncertain significance |
| rs374936361 | 3:42,201,846 | C/A | — | likely benign |
| rs56657651 | 3:42,218,299 | C/G | — | benign |
| rs1559877920 | 3:42,218,304 | A/C | — | pathogenic |
| rs777634059 | 3:42,218,346 | T/C | — | likely benign |
| rs764490967 | 3:42,218,353 | A/G | — | uncertain significance |
| rs564059529 | 3:42,218,369 | G/A | — | uncertain significance |
| rs2472512700 | 3:42,218,380 | G/A | — | uncertain significance |
| rs749888857 | 3:42,218,381 | A/T | — | uncertain significance |
| rs373727209 | 3:42,218,398 | G/A | — | likely benign |
| rs4234445 | 3:42,226,151 | T/C | — | benign |
| rs377073086 | 3:42,226,200 | C/T | — | likely benign |
| rs756303312 | 3:42,226,205 | G/A | — | uncertain significance |
| rs138576547 | 3:42,226,215 | G/C | — | uncertain significance |
| rs141558684 | 3:42,226,218 | G/A | — | likely benign |
| rs11544368 | 3:42,226,245 | C/G | — | likely benign |
| rs2472632192 | 3:42,226,260 | G/C | — | likely benign |
| rs1213000750 | 3:42,226,284 | C/G | — | uncertain significance |
| rs1375537 | 3:42,226,310 | C/T | — | benign |
| rs77415216 | 3:42,229,521 | T/C | — | benign |
| rs74685550 | 3:42,229,527 | G/T | — | benign |
| rs139582244 | 3:42,229,550 | G/A | — | uncertain significance |
| rs1423659055 | 3:42,229,570 | G/A | — | uncertain significance |
| rs1705161112 | 3:42,229,575 | G/T | — | uncertain significance |
| rs41289564 | 3:42,229,596 | C/T | — | likely benign |
| rs532538472 | 3:42,229,601 | C/T | — | uncertain significance |
| rs552538335 | 3:42,229,624 | G/A | — | uncertain significance |
| rs192413950 | 3:42,230,491 | C/T | — | benign |
| rs368538418 | 3:42,230,501 | C/T | — | likely benign |
| rs145279682 | 3:42,230,546 | A/G | — | conflicting classifications of pathogenicity |
| rs758664395 | 3:42,230,552 | A/G | — | uncertain significance |
| rs144666749 | 3:42,230,554 | T/C | — | likely benign |
| rs371843104 | 3:42,230,557 | G/A | — | uncertain significance |
| rs141503991 | 3:42,230,613 | C/T | — | likely benign |
| rs774131602 | 3:42,230,614 | G/A | — | uncertain significance |
| rs374727887 | 3:42,230,622 | G/T | — | uncertain significance |
| rs368834658 | 3:42,230,625 | C/G | — | likely benign |
| rs748755351 | 3:42,233,061 | G/A | — | likely benign |
| rs769986004 | 3:42,233,091 | G/A | — | likely benign |
| rs756546466 | 3:42,233,137 | C/T | — | likely benign |
| rs114345698 | 3:42,233,139 | G/A | — | benign |
| rs1706049367 | 3:42,234,555 | T/G | — | likely benign |
| rs1014846741 | 3:42,234,596 | T/G | — | uncertain significance |
| rs2149434745 | 3:42,234,623 | G/T | — | uncertain significance |
| rs778344493 | 3:42,234,632 | C/T | — | uncertain significance |
| rs768379461 | 3:42,234,653 | C/T | — | uncertain significance |
| rs145303759 | 3:42,234,663 | C/T | — | conflicting classifications of pathogenicity |
| rs1179269459 | 3:42,234,705 | T/C | — | likely benign |
| rs2290137 | 3:42,234,740 | G/A | — | benign |
| rs373539726 | 3:42,235,307 | A/G | — | likely benign |
| rs144162412 | 3:42,235,318 | C/T | — | benign |
| rs2149437708 | 3:42,235,335 | A/G | — | uncertain significance |
| rs60098029 | 3:42,235,345 | G/A | — | benign |
| rs2472782571 | 3:42,235,350 | T/C | — | uncertain significance |
| rs373149810 | 3:42,236,288 | G/T | — | likely benign |
| rs376331284 | 3:42,236,290 | C/T | — | likely benign |
| rs770281448 | 3:42,236,306 | T/C | — | uncertain significance |
| rs2149441749 | 3:42,236,314 | A/G | — | uncertain significance |
| rs2149441913 | 3:42,236,345 | A/T | — | uncertain significance |
| rs761614570 | 3:42,236,349 | G/T | — | likely benign |
| rs768244951 | 3:42,236,402 | G/A | — | uncertain significance |
| rs761561436 | 3:42,236,405 | G/A | — | uncertain significance |
| rs9851455 | 3:42,236,415 | A/G | — | benign |
| rs1193064633 | 3:42,236,423 | T/C | — | uncertain significance |
| rs1707175898 | 3:42,240,688 | T/C | — | uncertain significance |
| rs2149461152 | 3:42,240,701 | G/A | — | uncertain significance |
| rs146849711 | 3:42,240,717 | T/C | — | likely benign |
| rs140638437 | 3:42,240,728 | C/T | — | benign |
| rs200860677 | 3:42,240,729 | G/A | — | uncertain significance |
| rs372269973 | 3:42,240,733 | C/G | — | uncertain significance |
| rs143137647 | 3:42,240,749 | C/T | — | likely benign |
| rs770684926 | 3:42,240,750 | G/C | — | uncertain significance |
| rs761921574 | 3:42,242,334 | A/G | — | likely benign |
| rs1250319162 | 3:42,242,376 | C/T | — | likely benign |
Showing 100 of 224 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.