ANKS1A
ankyrin repeat and sterile alpha motif domain containing 1A
Summary
Predicted to enable ephrin receptor binding activity. Predicted to be involved in ephrin receptor signaling pathway; neuron remodeling; and substrate-dependent cell migration. Predicted to act upstream of or within negative regulation of ubiquitin-dependent protein catabolic process and regulation of ephrin receptor signaling pathway. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants101 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2533790738 | 6:34,857,183 | G/A | — | uncertain significance |
| rs779705410 | 6:34,857,358 | C/T | — | uncertain significance |
| rs192129212 | 6:34,873,421 | T/C | intron variant | — |
| rs143320464 | 6:34,882,626 | C/G | intron variant | — |
| rs12205331 | 6:34,898,455 | C/T | intron variant | — |
| rs191790731 | 6:34,905,100 | A/T | intron variant | — |
| rs847845 | 6:34,923,864 | G/C | — | — |
| rs1535001 | 6:34,927,280 | A/T | — | — |
| rs144626118 | 6:34,929,477 | A/G | intron variant | — |
| rs774910506 | 6:34,935,016 | C/T | — | likely benign |
| rs147758055 | 6:34,935,067 | C/G | — | likely benign |
| rs150247971 | 6:34,937,829 | C/T | — | likely benign |
| rs1249070807 | 6:34,937,851 | T/C | — | uncertain significance |
| rs2534189122 | 6:34,949,576 | T/G | — | uncertain significance |
| rs2534189559 | 6:34,949,631 | G/A | — | uncertain significance |
| rs748020550 | 6:34,949,731 | C/A | — | uncertain significance |
| rs114046576 | 6:34,949,894 | C/T | regulatory region variant | — |
| rs546233482 | 6:34,950,535 | A/G | — | uncertain significance |
| rs767137276 | 6:34,951,142 | A/C | — | uncertain significance |
| rs2534199255 | 6:34,951,191 | A/G | — | uncertain significance |
| rs147778746 | 6:34,952,981 | G/A | — | uncertain significance |
| rs199740223 | 6:34,957,010 | C/T | — | uncertain significance |
| rs561189520 | 6:34,959,534 | T/C | — | — |
| rs180811450 | 6:34,960,196 | G/A | intron variant | — |
| rs780259794 | 6:34,962,155 | C/G | — | uncertain significance |
| rs78397895 | 6:34,962,193 | A/G | — | benign |
| rs143079295 | 6:34,969,844 | G/A | intron variant | — |
| rs2140418 | 6:34,975,415 | T/A | — | — |
| rs138587834 | 6:34,985,115 | C/G | regulatory region variant | — |
| rs201532907 | 6:34,985,242 | A/G | — | likely benign |
| rs371173819 | 6:34,985,258 | C/T | — | uncertain significance |
| rs757203673 | 6:34,985,259 | G/A | — | uncertain significance |
| rs368400189 | 6:34,985,289 | C/T | — | uncertain significance |
| rs199969282 | 6:34,985,340 | G/A | — | uncertain significance |
| rs1282967751 | 6:34,985,357 | G/A | — | uncertain significance |
| rs755087986 | 6:34,985,393 | G/A | — | likely benign |
| rs1317773940 | 6:34,985,405 | C/T | — | uncertain significance |
| rs1259042771 | 6:34,985,414 | G/A | — | uncertain significance |
| rs760663991 | 6:34,985,439 | A/C | — | uncertain significance |
| rs1204105508 | 6:34,985,487 | C/A | — | uncertain significance |
| rs753164037 | 6:34,985,521 | A/C | — | uncertain significance |
| rs62402705 | 6:34,985,558 | C/G | — | benign |
| rs750583634 | 6:34,985,595 | C/T | — | uncertain significance |
| rs1471900150 | 6:34,985,621 | G/A | — | uncertain significance |
| rs188252688 | 6:34,985,624 | C/T | — | uncertain significance |
| rs369065359 | 6:34,985,640 | G/A | — | uncertain significance |
| rs761915621 | 6:34,985,654 | A/G | — | uncertain significance |
| rs35213739 | 6:34,985,716 | C/T | — | benign |
| rs77553288 | 6:34,985,774 | A/T | — | uncertain significance |
| rs771131808 | 6:34,985,808 | C/T | — | uncertain significance |
| rs2534350255 | 6:34,985,831 | G/A | — | uncertain significance |
| rs2258604 | 6:34,997,606 | T/A | intron variant | — |
| rs13210323 | 6:35,005,084 | A/T | — | — |
| rs2820224 | 6:35,009,578 | G/C | intron variant | — |
| rs2820230 | 6:35,012,829 | T/G | — | — |
| rs370362816 | 6:35,021,927 | C/T | — | uncertain significance |
| rs374619995 | 6:35,021,928 | G/A | — | likely benign |
| rs820093 | 6:35,023,110 | A/T | intron variant | — |
| rs776379008 | 6:35,027,929 | C/T | — | uncertain significance |
| rs763023596 | 6:35,027,943 | G/C | — | uncertain significance |
| rs200964525 | 6:35,027,962 | G/A | — | uncertain significance |
| rs779034710 | 6:35,027,969 | T/C | — | uncertain significance |
| rs1257206556 | 6:35,028,016 | G/A | — | uncertain significance |
| rs17609940 | 6:35,034,800 | G/A | — | — |
| rs820072 | 6:35,038,415 | T/A | — | — |
| rs2494097 | 6:35,044,057 | A/G | intron variant | — |
| rs2534666707 | 6:35,046,339 | C/G | — | uncertain significance |
| rs202219773 | 6:35,046,365 | C/T | — | uncertain significance |
| rs747607930 | 6:35,046,366 | G/A | — | uncertain significance |
| rs758393206 | 6:35,046,416 | G/T | — | uncertain significance |
| rs140739340 | 6:35,046,420 | G/A | — | uncertain significance |
| rs191850440 | 6:35,047,588 | C/T | — | benign |
| rs1158085982 | 6:35,047,599 | T/G | — | uncertain significance |
| rs368839668 | 6:35,047,656 | G/A | — | uncertain significance |
| rs2534679239 | 6:35,047,670 | C/G | — | uncertain significance |
| rs753822903 | 6:35,048,793 | C/T | — | uncertain significance |
| rs201109760 | 6:35,050,499 | G/A | — | uncertain significance |
| rs1249265846 | 6:35,050,516 | G/A | — | uncertain significance |
| rs149057322 | 6:35,050,531 | G/T | — | uncertain significance |
| rs34422534 | 6:35,050,593 | T/C | — | benign |
| rs138192177 | 6:35,050,963 | G/A | — | uncertain significance |
| rs757275006 | 6:35,050,986 | G/A | — | uncertain significance |
| rs371531749 | 6:35,051,232 | C/G | — | uncertain significance |
| rs201592159 | 6:35,051,266 | G/A | — | uncertain significance |
| rs369787709 | 6:35,051,923 | G/A | — | uncertain significance |
| rs529880264 | 6:35,051,993 | G/T | — | uncertain significance |
| rs138813662 | 6:35,052,027 | G/A | — | uncertain significance |
| rs749872435 | 6:35,053,611 | G/C | — | uncertain significance |
| rs146160816 | 6:35,053,635 | C/T | — | likely benign |
| rs199931805 | 6:35,053,636 | G/A | — | uncertain significance |
| rs201812720 | 6:35,053,676 | C/G | — | uncertain significance |
| rs202217863 | 6:35,053,677 | G/A | — | likely benign |
| rs140181302 | 6:35,053,695 | C/T | — | benign |
| rs143845391 | 6:35,053,711 | G/A | — | uncertain significance |
| rs4276486 | 6:35,054,672 | G/T | — | — |
| rs150867713 | 6:35,054,745 | T/C | — | likely benign |
| rs2005 | 6:35,056,443 | A/T | — | — |
| rs140103824 | 6:35,057,497 | T/G | regulatory region variant | — |
| rs186447074 | 6:35,059,131 | T/C | 3 prime UTR variant | — |
| rs2689096 | 6:35,061,714 | G/C | downstream gene variant | — |
Showing 100 of 101 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.