GAS7
growth arrest specific 7
Summary
Growth arrest-specific 7 is expressed primarily in terminally differentiated brain cells and predominantly in mature cerebellar Purkinje neurons. GAS7 plays a putative role in neuronal development. Several transcript variants encoding proteins which vary in the N-terminus have been described. [provided by RefSeq, Jul 2008]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2286532 | 17:9,820,278 | T/C | — | benign |
| rs778281299 | 17:9,820,619 | G/C | — | uncertain significance |
| rs2543681746 | 17:9,820,658 | T/A | — | uncertain significance |
| rs4791910 | 17:9,820,695 | T/C | — | benign |
| rs11078821 | 17:9,820,739 | G/A | — | benign |
| rs57391370 | 17:9,820,753 | G/C | — | benign |
| rs16958993 | 17:9,820,831 | C/A | — | benign |
| rs59994052 | 17:9,820,883 | T/C | — | benign |
| rs9908886 | 17:9,821,123 | G/C | — | benign |
| rs11078822 | 17:9,821,249 | T/C | — | benign |
| rs62064494 | 17:9,821,452 | C/T | — | benign |
| rs2270122 | 17:9,821,474 | C/T | — | benign |
| rs9916639 | 17:9,821,585 | T/C | — | benign |
| rs55976773 | 17:9,821,618 | T/G | — | benign |
| rs9897353 | 17:9,822,758 | T/C | — | benign |
| rs776365443 | 17:9,822,974 | T/C | — | uncertain significance |
| rs12453300 | 17:9,828,516 | T/C | — | benign |
| rs11657901 | 17:9,829,256 | T/C | — | benign |
| rs11652174 | 17:9,829,633 | C/T | — | benign |
| rs11651891 | 17:9,829,666 | G/C | — | benign |
| rs11651894 | 17:9,829,681 | G/A | — | benign |
| rs7216815 | 17:9,829,886 | G/T | — | benign |
| rs146733108 | 17:9,829,984 | C/A | — | benign |
| rs1004133470 | 17:9,830,017 | C/T | — | uncertain significance |
| rs2543766397 | 17:9,830,052 | A/G | — | uncertain significance |
| rs7218907 | 17:9,830,100 | A/G | — | benign |
| rs56199323 | 17:9,830,171 | C/T | — | benign |
| rs17745519 | 17:9,830,294 | C/A | — | benign |
| rs10852918 | 17:9,840,501 | A/G | regulatory region variant | — |
| rs75455559 | 17:9,843,216 | A/G | — | benign |
| rs1193959575 | 17:9,843,515 | A/G | — | uncertain significance |
| rs11654620 | 17:9,846,274 | G/T | — | benign |
| rs2240740 | 17:9,846,365 | G/A | — | benign |
| rs2240741 | 17:9,846,389 | G/A | — | benign |
| rs756539206 | 17:9,846,447 | A/G | — | uncertain significance |
| rs150413928 | 17:9,846,520 | C/T | — | uncertain significance |
| rs17339499 | 17:9,846,521 | G/C | — | benign |
| rs774386040 | 17:9,846,523 | T/C | — | uncertain significance |
| rs2068669205 | 17:9,846,525 | C/G | — | uncertain significance |
| rs111906980 | 17:9,846,527 | G/A | — | benign |
| rs2543907770 | 17:9,846,531 | C/T | — | uncertain significance |
| rs8066006 | 17:9,846,631 | G/A | — | benign |
| rs733804 | 17:9,846,724 | A/C | — | benign |
| rs9901715 | 17:9,850,129 | A/G | — | benign |
| rs763337191 | 17:9,850,269 | G/A | — | uncertain significance |
| rs34907720 | 17:9,850,286 | C/T | — | benign |
| rs62064532 | 17:9,850,440 | C/T | — | benign |
| rs76539195 | 17:9,850,479 | C/G | — | benign |
| rs77892008 | 17:9,862,999 | T/C | — | benign |
| rs2277689 | 17:9,872,768 | A/G | — | benign |
| rs2277688 | 17:9,872,978 | C/T | — | benign |
| rs992195927 | 17:9,873,026 | T/C | — | uncertain significance |
| rs141181301 | 17:9,873,043 | G/A | — | uncertain significance |
| rs3786094 | 17:9,875,205 | T/G | — | — |
| rs150719505 | 17:9,885,186 | C/T | — | uncertain significance |
| rs3786080 | 17:9,906,554 | G/A | intron variant | — |
| rs35318670 | 17:9,923,096 | T/C | — | uncertain significance |
| rs774584393 | 17:9,923,121 | G/A | — | uncertain significance |
| rs772105221 | 17:9,923,123 | C/T | — | uncertain significance |
| rs765276902 | 17:9,923,124 | G/A | — | uncertain significance |
| rs2544416355 | 17:9,923,127 | C/T | — | uncertain significance |
| rs200563905 | 17:9,923,189 | G/A | — | uncertain significance |
| rs12936070 | 17:10,026,855 | C/T | intron variant | — |
| rs12150284 | 17:10,031,090 | C/G | — | — |
| rs9913911 | 17:10,031,183 | A/G | regulatory region variant | — |
| rs9914258 | 17:10,031,642 | C/T | regulatory region variant | — |
| rs11656696 | 17:10,033,679 | C/G | — | — |
| rs190657874 | 17:10,094,466 | T/G | intron variant | — |
| rs1043030029 | 17:10,101,650 | C/T | — | uncertain significance |
| rs897300611 | 17:10,101,653 | G/C | — | uncertain significance |
| rs1045814146 | 17:10,101,659 | G/T | — | uncertain significance |
| rs1175033266 | 17:10,101,661 | C/T | — | uncertain significance |
| rs746150159 | 17:10,101,697 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.