ALS2CL
ALS2 C-terminal like
Summary
Predicted to enable guanyl-nucleotide exchange factor activity and small GTPase binding activity. Predicted to be involved in endosomal transport. Predicted to act upstream of or within protein localization. Predicted to be located in cytosol. Predicted to be active in cytoplasmic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1317391854 | 3:46,712,484 | T/A | — | uncertain significance |
| rs149150920 | 3:46,712,514 | T/C | — | uncertain significance |
| rs146989129 | 3:46,713,032 | C/G | — | uncertain significance |
| rs201782392 | 3:46,713,381 | G/A | — | uncertain significance |
| rs368356424 | 3:46,713,474 | C/T | — | uncertain significance |
| rs144505150 | 3:46,713,518 | G/A | — | uncertain significance |
| rs548058222 | 3:46,713,633 | A/T | — | uncertain significance |
| rs536135476 | 3:46,714,158 | C/T | — | — |
| rs753608122 | 3:46,716,194 | A/T | — | uncertain significance |
| rs142447205 | 3:46,717,117 | G/C | — | uncertain significance |
| rs554056115 | 3:46,717,150 | C/T | — | uncertain significance |
| rs375865019 | 3:46,717,151 | G/A | — | uncertain significance |
| rs139670900 | 3:46,717,165 | C/T | — | likely benign |
| rs189714038 | 3:46,717,784 | C/T | — | uncertain significance |
| rs948334223 | 3:46,717,790 | C/T | — | uncertain significance |
| rs565114772 | 3:46,717,811 | C/T | — | uncertain significance |
| rs374984971 | 3:46,717,852 | C/T | — | uncertain significance |
| rs373448357 | 3:46,718,157 | T/C | — | uncertain significance |
| rs1559463241 | 3:46,718,197 | C/T | — | uncertain significance |
| rs1191468116 | 3:46,718,215 | C/T | — | uncertain significance |
| rs2528671157 | 3:46,718,363 | G/A | — | uncertain significance |
| rs752570654 | 3:46,718,376 | C/T | — | uncertain significance |
| rs138602401 | 3:46,718,391 | C/A | — | uncertain significance |
| rs772104486 | 3:46,718,478 | G/A | — | uncertain significance |
| rs2528677756 | 3:46,719,816 | C/T | — | uncertain significance |
| rs112747072 | 3:46,720,718 | G/T | — | uncertain significance |
| rs775178920 | 3:46,721,924 | G/A | — | likely benign |
| rs780010917 | 3:46,721,969 | G/T | — | uncertain significance |
| rs140756490 | 3:46,721,988 | C/T | — | uncertain significance |
| rs369892563 | 3:46,722,817 | T/G | — | uncertain significance |
| rs369393379 | 3:46,722,851 | G/A | — | uncertain significance |
| rs200364692 | 3:46,723,084 | C/T | — | uncertain significance |
| rs371712521 | 3:46,723,559 | G/A | — | uncertain significance |
| rs139939925 | 3:46,723,567 | G/A | — | uncertain significance |
| rs190519069 | 3:46,723,843 | C/A | intron variant | — |
| rs55842118 | 3:46,724,638 | C/T | — | uncertain significance |
| rs202007681 | 3:46,724,674 | C/T | — | uncertain significance |
| rs372117335 | 3:46,724,708 | G/A | — | uncertain significance |
| rs368302960 | 3:46,724,750 | C/G | — | uncertain significance |
| rs771043850 | 3:46,724,776 | G/A | — | likely benign |
| rs541431840 | 3:46,725,294 | C/G | — | uncertain significance |
| rs761184463 | 3:46,725,322 | G/A | — | uncertain significance |
| rs142502930 | 3:46,727,052 | C/T | — | uncertain significance |
| rs770642378 | 3:46,727,851 | C/G | — | uncertain significance |
| rs2528709074 | 3:46,727,857 | C/T | — | uncertain significance |
| rs2528709309 | 3:46,727,914 | C/G | — | uncertain significance |
| rs371027094 | 3:46,727,916 | C/T | — | likely benign |
| rs931833077 | 3:46,728,484 | T/A | — | uncertain significance |
| rs531434171 | 3:46,728,511 | C/T | — | uncertain significance |
| rs368009065 | 3:46,728,539 | C/A | — | uncertain significance |
| rs556037923 | 3:46,728,556 | C/T | — | uncertain significance |
| rs376089110 | 3:46,728,573 | G/A | — | uncertain significance |
| rs761173942 | 3:46,728,607 | G/A | — | uncertain significance |
| rs536570568 | 3:46,728,628 | G/A | — | uncertain significance |
| rs1223015086 | 3:46,729,151 | C/T | — | uncertain significance |
| rs200224258 | 3:46,729,609 | C/T | — | uncertain significance |
| rs144978241 | 3:46,729,610 | G/A | — | uncertain significance |
| rs1385815839 | 3:46,729,621 | C/T | — | uncertain significance |
| rs138023761 | 3:46,729,649 | T/C | — | uncertain significance |
| rs1429382526 | 3:46,729,735 | T/C | — | uncertain significance |
| rs1699934740 | 3:46,729,756 | T/G | — | uncertain significance |
| rs765382733 | 3:46,729,774 | G/A | — | uncertain significance |
| rs143925967 | 3:46,730,900 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.