ASTN1
astrotactin 1
Summary
Astrotactin is a neuronal adhesion molecule required for glial-guided migration of young postmitotic neuroblasts in cortical regions of developing brain, including cerebrum, hippocampus, cerebellum, and olfactory bulb (Fink et al., 1995).[supplied by OMIM, Jun 2009]
Known Variants93 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61756323 | 1:176,833,427 | T/C | — | likely benign |
| rs200271835 | 1:176,833,454 | G/A | — | uncertain significance |
| rs144824957 | 1:176,833,480 | C/T | — | likely benign |
| rs368198179 | 1:176,833,496 | C/T | — | uncertain significance |
| rs538221544 | 1:176,833,536 | C/T | — | uncertain significance |
| rs148482637 | 1:176,833,571 | C/T | — | likely benign |
| rs778485570 | 1:176,833,574 | C/T | — | uncertain significance |
| rs1553217993 | 1:176,838,112 | T/A | — | not provided |
| rs767323181 | 1:176,845,694 | C/T | — | uncertain significance |
| rs138978807 | 1:176,845,721 | C/T | — | uncertain significance |
| rs778027121 | 1:176,845,724 | C/T | — | uncertain significance |
| rs375249247 | 1:176,845,752 | G/T | — | uncertain significance |
| rs1460495222 | 1:176,852,017 | G/C | — | uncertain significance |
| rs199961480 | 1:176,852,023 | G/A | — | likely pathogenic |
| rs151246825 | 1:176,852,074 | T/G | — | conflicting classifications of pathogenicity |
| rs558363072 | 1:176,853,487 | T/G | — | uncertain significance |
| rs201593312 | 1:176,853,522 | C/T | — | uncertain significance |
| rs143440206 | 1:176,853,612 | G/A | — | conflicting classifications of pathogenicity |
| rs1204954294 | 1:176,857,208 | C/G | — | uncertain significance |
| rs1669115841 | 1:176,857,289 | C/T | — | uncertain significance |
| rs543065232 | 1:176,863,753 | T/A | — | uncertain significance |
| rs1224263248 | 1:176,863,775 | G/C | — | uncertain significance |
| rs948124986 | 1:176,863,814 | A/T | — | uncertain significance |
| rs759502995 | 1:176,863,868 | G/A | — | uncertain significance |
| rs777093050 | 1:176,863,937 | G/A | — | uncertain significance |
| rs745642391 | 1:176,863,960 | G/A | — | uncertain significance |
| rs147230008 | 1:176,866,100 | C/T | intron variant | — |
| rs376533414 | 1:176,903,282 | A/G | — | likely benign |
| rs199937923 | 1:176,903,320 | C/T | — | uncertain significance |
| rs374641554 | 1:176,903,420 | C/T | — | uncertain significance |
| rs752511585 | 1:176,905,439 | C/T | — | uncertain significance |
| rs781276168 | 1:176,905,450 | G/A | — | uncertain significance |
| rs2526662890 | 1:176,905,495 | A/G | — | uncertain significance |
| rs780039050 | 1:176,913,102 | C/T | — | uncertain significance |
| rs138686233 | 1:176,915,087 | C/T | missense variant | likely pathogenic |
| rs202163703 | 1:176,915,167 | C/G | — | uncertain significance |
| rs142811346 | 1:176,915,207 | T/A | — | uncertain significance |
| rs372931394 | 1:176,915,221 | C/T | — | uncertain significance |
| rs2526729378 | 1:176,915,227 | T/C | — | uncertain significance |
| rs2526749434 | 1:176,918,342 | T/C | — | uncertain significance |
| rs779839895 | 1:176,918,438 | C/T | — | uncertain significance |
| rs1244131323 | 1:176,918,465 | A/G | — | uncertain significance |
| rs144761357 | 1:176,926,816 | C/T | — | uncertain significance |
| rs564780987 | 1:176,926,854 | C/T | — | uncertain significance |
| rs770266633 | 1:176,926,902 | G/A | — | uncertain significance |
| rs201822123 | 1:176,926,903 | G/A | — | uncertain significance |
| rs2526803759 | 1:176,926,924 | C/A | — | uncertain significance |
| rs367797381 | 1:176,926,950 | G/A | — | uncertain significance |
| rs2526810484 | 1:176,927,533 | A/G | — | uncertain significance |
| rs768516101 | 1:176,927,593 | T/C | — | uncertain significance |
| rs192406167 | 1:176,934,370 | T/C | — | likely benign |
| rs752367629 | 1:176,983,952 | G/T | — | likely benign |
| rs377210940 | 1:176,992,546 | C/T | — | uncertain significance |
| rs368908680 | 1:176,992,558 | G/C | — | uncertain significance |
| rs2525289417 | 1:176,992,649 | A/G | — | likely benign |
| rs928305031 | 1:176,993,720 | A/C | — | uncertain significance |
| rs758518322 | 1:176,993,734 | G/T | — | uncertain significance |
| rs556443561 | 1:176,993,764 | C/T | — | uncertain significance |
| rs140196066 | 1:176,993,779 | C/T | — | uncertain significance |
| rs1676013054 | 1:176,993,835 | G/A | — | uncertain significance |
| rs1474333732 | 1:176,993,844 | T/C | — | uncertain significance |
| rs753290063 | 1:176,998,774 | A/C | — | uncertain significance |
| rs148425095 | 1:176,998,778 | C/T | — | uncertain significance |
| rs749890033 | 1:176,998,779 | G/A | — | uncertain significance |
| rs2101970440 | 1:176,998,821 | G/T | — | uncertain significance |
| rs202183126 | 1:176,998,832 | G/A | — | uncertain significance |
| rs765739439 | 1:176,998,850 | C/T | — | uncertain significance |
| rs777585445 | 1:176,999,954 | T/C | — | uncertain significance |
| rs143274107 | 1:176,999,963 | G/C | — | uncertain significance |
| rs2525338152 | 1:176,999,965 | T/C | — | uncertain significance |
| rs781283066 | 1:177,000,086 | T/C | — | uncertain significance |
| rs757553489 | 1:177,001,651 | G/A | — | uncertain significance |
| rs938499885 | 1:177,001,735 | C/T | — | uncertain significance |
| rs751725406 | 1:177,001,736 | C/T | — | uncertain significance |
| rs756552002 | 1:177,001,756 | C/T | — | uncertain significance |
| rs780426972 | 1:177,001,838 | C/T | — | uncertain significance |
| rs6697602 | 1:177,039,372 | C/G | intron variant | — |
| rs16850767 | 1:177,091,795 | C/T | intron variant | — |
| rs57530364 | 1:177,096,284 | T/A | intron variant | — |
| rs12096344 | 1:177,125,420 | C/T | — | — |
| rs571716453 | 1:177,126,238 | T/C | — | — |
| rs11577430 | 1:177,129,012 | C/G | intron variant | — |
| rs1281225900 | 1:177,133,536 | C/A | — | uncertain significance |
| rs1229151646 | 1:177,133,655 | A/G | — | uncertain significance |
| rs780341371 | 1:177,133,668 | G/T | — | uncertain significance |
| rs142162197 | 1:177,133,734 | C/T | — | uncertain significance |
| rs2526138128 | 1:177,133,736 | T/G | — | uncertain significance |
| rs755134545 | 1:177,133,747 | C/G | — | likely benign |
| rs2102275014 | 1:177,133,749 | T/G | — | uncertain significance |
| rs1647609978 | 1:177,133,757 | A/C | — | uncertain significance |
| rs2526138576 | 1:177,133,759 | C/G | — | likely benign |
| rs1310821264 | 1:177,133,767 | G/C | — | uncertain significance |
| rs2526139188 | 1:177,133,800 | C/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.