TOM1
target of myb1 membrane trafficking protein
Summary
This gene was identified as a target of the v-myb oncogene. The encoded protein shares its N-terminal domain in common with proteins associated with vesicular trafficking at the endosome. It is recruited to the endosomes by its interaction with endofin. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4461 | 22:35,695,802 | G/A | — | benign |
| rs1396819307 | 22:35,695,971 | T/G | — | uncertain significance |
| rs138728 | 22:35,696,077 | C/G | — | benign |
| rs138740 | 22:35,699,582 | C/T | upstream gene variant | — |
| rs138742 | 22:35,699,759 | G/T | — | — |
| rs138747 | 22:35,700,488 | A/C | — | — |
| rs3788509 | 22:35,707,236 | G/A | regulatory region variant | — |
| rs138777 | 22:35,711,098 | A/G | intron variant | — |
| rs555423294 | 22:35,713,862 | C/A | — | uncertain significance |
| rs373113007 | 22:35,713,899 | G/A | — | uncertain significance |
| rs57755951 | 22:35,713,931 | C/T | — | benign |
| rs768517941 | 22:35,713,935 | A/G | — | uncertain significance |
| rs2517741938 | 22:35,717,946 | C/T | — | uncertain significance |
| rs780990957 | 22:35,717,989 | G/A | — | uncertain significance |
| rs11558473 | 22:35,719,055 | G/A | — | uncertain significance |
| rs367816016 | 22:35,719,072 | G/A | — | uncertain significance |
| rs761517973 | 22:35,719,160 | A/G | — | uncertain significance |
| rs189410945 | 22:35,719,352 | T/C | intron variant | — |
| rs926916292 | 22:35,719,501 | G/A | — | uncertain significance |
| rs771648997 | 22:35,719,519 | G/A | — | uncertain significance |
| rs1928034490 | 22:35,719,534 | G/T | — | uncertain significance |
| rs764578585 | 22:35,719,556 | G/A | — | uncertain significance |
| rs763314023 | 22:35,719,619 | A/G | — | likely benign |
| rs371088274 | 22:35,719,764 | G/A | — | uncertain significance |
| rs2517750236 | 22:35,719,788 | G/A | — | uncertain significance |
| rs140576566 | 22:35,719,875 | G/A | — | likely benign |
| rs61731679 | 22:35,723,320 | G/A | — | benign |
| rs1408644431 | 22:35,723,331 | C/T | — | uncertain significance |
| rs1928423768 | 22:35,723,346 | C/T | — | uncertain significance |
| rs201441903 | 22:35,723,360 | G/A | — | uncertain significance |
| rs34371697 | 22:35,726,364 | A/G | — | conflicting classifications of pathogenicity |
| rs1430211343 | 22:35,726,368 | A/G | — | uncertain significance |
| rs770654000 | 22:35,726,400 | G/A | — | uncertain significance |
| rs369952232 | 22:35,726,404 | A/G | — | conflicting classifications of pathogenicity |
| rs191996137 | 22:35,726,464 | G/T | — | uncertain significance |
| rs780156731 | 22:35,728,982 | G/A | — | uncertain significance |
| rs749192174 | 22:35,728,988 | G/A | — | uncertain significance |
| rs2517777752 | 22:35,728,993 | G/T | — | uncertain significance |
| rs778537779 | 22:35,728,994 | G/A | — | pathogenic |
| rs771548371 | 22:35,729,418 | G/T | — | uncertain significance |
| rs775808746 | 22:35,729,433 | G/A | — | uncertain significance |
| rs557799756 | 22:35,729,460 | G/A | — | likely benign |
| rs571208836 | 22:35,729,481 | G/A | — | uncertain significance |
| rs377303679 | 22:35,730,410 | C/T | — | uncertain significance |
| rs750391365 | 22:35,730,411 | G/A | — | uncertain significance |
| rs146200939 | 22:35,730,426 | C/T | — | likely benign |
| rs199955093 | 22:35,734,736 | C/T | — | likely benign |
| rs771996974 | 22:35,734,757 | C/A | — | uncertain significance |
| rs773071776 | 22:35,734,758 | G/C | — | uncertain significance |
| rs149877665 | 22:35,734,779 | G/A | — | uncertain significance |
| rs757629430 | 22:35,734,780 | C/T | — | uncertain significance |
| rs766541001 | 22:35,741,725 | T/C | — | uncertain significance |
| rs1252471665 | 22:35,741,758 | A/T | — | uncertain significance |
| rs133398 | 22:35,741,820 | G/A | — | benign |
| rs133399 | 22:35,741,863 | G/A | — | benign |
| rs743810 | 22:35,742,925 | T/G | — | benign |
| rs117763819 | 22:35,743,090 | G/A | — | uncertain significance |
| rs144721465 | 22:35,743,105 | C/T | — | uncertain significance |
| rs2071745 | 22:35,743,124 | G/C | — | benign |
| rs756574663 | 22:35,743,138 | C/G | — | uncertain significance |
| rs368486186 | 22:35,743,150 | C/T | — | uncertain significance |
| rs774644191 | 22:35,743,153 | C/T | — | uncertain significance |
| rs140465923 | 22:35,743,178 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.