TSGA10IP
testis specific 10 interacting protein
Summary
Predicted to be involved in cilium organization. Predicted to be located in cytoskeleton. Predicted to be active in photoreceptor connecting cilium. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1355804945 | 11:65,713,151 | G/A | — | uncertain significance |
| rs183731710 | 11:65,713,205 | T/C | — | likely benign |
| rs1394564440 | 11:65,713,226 | G/A | — | uncertain significance |
| rs1450938799 | 11:65,713,265 | T/G | — | uncertain significance |
| rs753043188 | 11:65,713,271 | C/T | — | uncertain significance |
| rs770922079 | 11:65,713,274 | C/T | — | uncertain significance |
| rs749210046 | 11:65,713,276 | G/A | — | likely benign |
| rs377282930 | 11:65,714,435 | C/T | — | uncertain significance |
| rs200493850 | 11:65,714,452 | G/C | — | uncertain significance |
| rs192876608 | 11:65,714,472 | C/A | — | uncertain significance |
| rs545969622 | 11:65,714,615 | C/A | — | uncertain significance |
| rs961186840 | 11:65,714,639 | A/T | — | likely benign |
| rs759743147 | 11:65,714,727 | G/A | — | likely benign |
| rs376751149 | 11:65,714,738 | C/A | — | uncertain significance |
| rs775763229 | 11:65,714,739 | G/A | — | uncertain significance |
| rs185403886 | 11:65,714,766 | C/T | — | uncertain significance |
| rs200322456 | 11:65,714,793 | C/T | — | likely benign |
| rs2495716068 | 11:65,714,804 | A/C | — | uncertain significance |
| rs570917824 | 11:65,714,807 | G/C | — | uncertain significance |
| rs370190488 | 11:65,714,843 | A/G | — | uncertain significance |
| rs1421063432 | 11:65,714,876 | C/T | — | uncertain significance |
| rs2495716609 | 11:65,714,877 | C/T | — | uncertain significance |
| rs747536456 | 11:65,714,885 | G/T | — | uncertain significance |
| rs769560691 | 11:65,714,903 | A/G | — | uncertain significance |
| rs761714052 | 11:65,714,922 | C/T | — | uncertain significance |
| rs568806221 | 11:65,714,939 | G/T | — | uncertain significance |
| rs199784761 | 11:65,714,953 | C/G | — | uncertain significance |
| rs769052660 | 11:65,714,972 | G/A | — | uncertain significance |
| rs777964930 | 11:65,715,118 | G/T | — | uncertain significance |
| rs1467207313 | 11:65,715,144 | C/T | — | uncertain significance |
| rs767010738 | 11:65,715,153 | G/A | — | uncertain significance |
| rs71455793 | 11:65,715,204 | G/A | coding sequence variant | — |
| rs931691028 | 11:65,715,244 | G/C | — | uncertain significance |
| rs1015050658 | 11:65,715,503 | G/T | — | uncertain significance |
| rs750562368 | 11:65,715,526 | G/A | — | likely benign |
| rs758257299 | 11:65,715,543 | G/A | — | uncertain significance |
| rs1400825410 | 11:65,715,561 | A/T | — | uncertain significance |
| rs367868269 | 11:65,715,567 | G/A | — | uncertain significance |
| rs2495721292 | 11:65,715,580 | T/C | — | uncertain significance |
| rs199848127 | 11:65,715,588 | C/T | — | uncertain significance |
| rs188103133 | 11:65,715,589 | G/A | — | uncertain significance |
| rs758452043 | 11:65,715,603 | C/G | — | uncertain significance |
| rs371057516 | 11:65,721,100 | G/A | — | uncertain significance |
| rs761786410 | 11:65,721,130 | T/G | — | uncertain significance |
| rs574976075 | 11:65,721,159 | A/G | — | uncertain significance |
| rs778814461 | 11:65,726,371 | G/A | — | uncertain significance |
| rs1317606626 | 11:65,726,670 | C/G | — | uncertain significance |
| rs377217355 | 11:65,726,686 | G/A | — | uncertain significance |
| rs767599562 | 11:65,727,353 | C/A | — | uncertain significance |
| rs376240417 | 11:65,727,391 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.