ARL6IP4
ARF like GTPase 6 interacting protein 4
Summary
Enables identical protein binding activity. Predicted to be involved in RNA splicing. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs767540748 | 12:123,464,975 | G/A | — | uncertain significance |
| rs1476805993 | 12:123,464,992 | C/T | — | uncertain significance |
| rs1223451827 | 12:123,465,014 | T/C | — | uncertain significance |
| rs911815820 | 12:123,465,037 | G/T | — | uncertain significance |
| rs2547502108 | 12:123,465,070 | A/G | — | uncertain significance |
| rs1054010058 | 12:123,465,098 | G/A | — | uncertain significance |
| rs747457503 | 12:123,465,139 | C/G | — | uncertain significance |
| rs1302122844 | 12:123,465,194 | G/A | — | uncertain significance |
| rs973346304 | 12:123,465,221 | C/T | — | uncertain significance |
| rs772645684 | 12:123,465,229 | T/G | — | uncertain significance |
| rs935629108 | 12:123,465,265 | G/A | — | uncertain significance |
| rs2037605211 | 12:123,465,269 | T/C | — | uncertain significance |
| rs1367350670 | 12:123,465,284 | G/A | — | uncertain significance |
| rs374152314 | 12:123,465,684 | G/A | — | uncertain significance |
| rs772860968 | 12:123,465,751 | A/C | — | uncertain significance |
| rs1179493491 | 12:123,465,777 | G/A | — | uncertain significance |
| rs763050821 | 12:123,465,834 | C/T | — | likely benign |
| rs55742290 | 12:123,466,111 | C/T | splice region variant | — |
| rs201538831 | 12:123,466,159 | G/A | — | uncertain significance |
| rs779795298 | 12:123,466,220 | C/T | — | uncertain significance |
| rs201978657 | 12:123,466,226 | C/T | — | uncertain significance |
| rs377049391 | 12:123,466,232 | C/T | — | uncertain significance |
| rs370149672 | 12:123,466,258 | C/T | — | uncertain significance |
| rs1466756531 | 12:123,466,341 | G/C | — | uncertain significance |
| rs2547510668 | 12:123,466,382 | T/C | — | uncertain significance |
| rs544394901 | 12:123,466,396 | C/G | — | uncertain significance |
| rs781416302 | 12:123,466,512 | G/T | — | uncertain significance |
| rs141764091 | 12:123,466,572 | C/T | — | uncertain significance |
| rs150474661 | 12:123,466,573 | G/A | — | uncertain significance |
| rs756356882 | 12:123,466,587 | C/T | — | uncertain significance |
| rs137934270 | 12:123,467,053 | G/A | — | uncertain significance |
| rs747841359 | 12:123,467,057 | C/T | — | uncertain significance |
| rs775426499 | 12:123,467,065 | C/G | — | uncertain significance |
| rs771187096 | 12:123,467,070 | C/G | — | uncertain significance |
| rs557381391 | 12:123,467,076 | G/C | — | uncertain significance |
| rs1184433271 | 12:123,467,077 | A/C | — | uncertain significance |
| rs568298382 | 12:123,467,192 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.