SIDT1
SID1 transmembrane family member 1
Summary
The protein encoded by this gene belongs to SID1 family of transmembrane dsRNA-gated channels. Family members transport dsRNA into cells and are required for systemic RNA interference. [provided by RefSeq, May 2017]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs936244012 | 3:113,251,879 | G/A | — | uncertain significance |
| rs546249779 | 3:113,251,899 | T/C | — | uncertain significance |
| rs150463419 | 3:113,251,995 | G/A | — | uncertain significance |
| rs141331686 | 3:113,252,049 | G/C | — | uncertain significance |
| rs7611694 | 3:113,275,624 | A/C | intron variant | — |
| rs7645464 | 3:113,284,492 | G/A | intron variant | — |
| rs1348670407 | 3:113,285,340 | A/G | — | uncertain significance |
| rs2474692979 | 3:113,286,401 | A/G | — | uncertain significance |
| rs774565755 | 3:113,286,494 | C/A | — | uncertain significance |
| rs13092825 | 3:113,290,468 | T/G | — | — |
| rs4682495 | 3:113,290,793 | A/T | — | — |
| rs28674622 | 3:113,292,637 | C/A | intron variant | — |
| rs1567780 | 3:113,294,482 | T/G | — | — |
| rs749283824 | 3:113,302,274 | G/A | — | uncertain significance |
| rs1436670975 | 3:113,302,303 | G/T | — | uncertain significance |
| rs150412083 | 3:113,302,320 | G/A | — | uncertain significance |
| rs149555257 | 3:113,303,548 | A/G | — | uncertain significance |
| rs1001306623 | 3:113,303,560 | C/G | — | uncertain significance |
| rs372768021 | 3:113,303,575 | G/A | — | uncertain significance |
| rs12489267 | 3:113,308,412 | G/T | — | — |
| rs147404509 | 3:113,311,875 | G/T | — | uncertain significance |
| rs1461364458 | 3:113,311,878 | G/A | — | uncertain significance |
| rs1041952012 | 3:113,320,480 | C/A | — | uncertain significance |
| rs139188815 | 3:113,321,906 | C/T | — | uncertain significance |
| rs201151023 | 3:113,321,919 | C/A | — | uncertain significance |
| rs377190997 | 3:113,321,935 | G/C | — | uncertain significance |
| rs765520373 | 3:113,321,990 | G/T | — | uncertain significance |
| rs555089942 | 3:113,322,844 | G/A | — | uncertain significance |
| rs2475144785 | 3:113,323,762 | T/C | — | uncertain significance |
| rs572675919 | 3:113,325,904 | G/C | — | uncertain significance |
| rs1324024594 | 3:113,326,982 | T/C | — | uncertain significance |
| rs368901751 | 3:113,327,012 | G/A | — | uncertain significance |
| rs201731979 | 3:113,327,015 | G/A | — | uncertain significance |
| rs146992283 | 3:113,327,029 | C/T | — | uncertain significance |
| rs199652698 | 3:113,327,030 | G/A | — | uncertain significance |
| rs144146634 | 3:113,327,302 | G/T | — | uncertain significance |
| rs773252869 | 3:113,327,330 | G/A | — | uncertain significance |
| rs761035881 | 3:113,327,332 | G/A | — | uncertain significance |
| rs1431057859 | 3:113,329,891 | T/C | — | uncertain significance |
| rs371176236 | 3:113,329,980 | G/A | — | uncertain significance |
| rs759257073 | 3:113,330,954 | T/C | — | uncertain significance |
| rs2475278415 | 3:113,330,975 | G/T | — | uncertain significance |
| rs147067311 | 3:113,330,984 | G/A | — | likely benign |
| rs2475278716 | 3:113,330,991 | C/A | — | uncertain significance |
| rs775256597 | 3:113,331,037 | G/C | — | uncertain significance |
| rs371641054 | 3:113,334,968 | C/T | — | uncertain significance |
| rs1946088101 | 3:113,335,007 | G/T | — | uncertain significance |
| rs765942083 | 3:113,338,561 | T/A | — | uncertain significance |
| rs1211362767 | 3:113,342,282 | T/C | — | uncertain significance |
| rs2475482441 | 3:113,342,321 | T/C | — | uncertain significance |
| rs531258462 | 3:113,342,377 | A/G | — | likely benign |
| rs747866418 | 3:113,342,575 | T/C | — | uncertain significance |
| rs377126190 | 3:113,344,953 | C/T | — | uncertain significance |
| rs374060767 | 3:113,344,980 | G/A | — | uncertain significance |
| rs199937260 | 3:113,344,982 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.