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

rsidPosition (GRCh37)AllelesClassClinVar
rs228653217:9,820,278T/Cbenign
rs77828129917:9,820,619G/Cuncertain significance
rs254368174617:9,820,658T/Auncertain significance
rs479191017:9,820,695T/Cbenign
rs1107882117:9,820,739G/Abenign
rs5739137017:9,820,753G/Cbenign
rs1695899317:9,820,831C/Abenign
rs5999405217:9,820,883T/Cbenign
rs990888617:9,821,123G/Cbenign
rs1107882217:9,821,249T/Cbenign
rs6206449417:9,821,452C/Tbenign
rs227012217:9,821,474C/Tbenign
rs991663917:9,821,585T/Cbenign
rs5597677317:9,821,618T/Gbenign
rs989735317:9,822,758T/Cbenign
rs77636544317:9,822,974T/Cuncertain significance
rs1245330017:9,828,516T/Cbenign
rs1165790117:9,829,256T/Cbenign
rs1165217417:9,829,633C/Tbenign
rs1165189117:9,829,666G/Cbenign
rs1165189417:9,829,681G/Abenign
rs721681517:9,829,886G/Tbenign
rs14673310817:9,829,984C/Abenign
rs100413347017:9,830,017C/Tuncertain significance
rs254376639717:9,830,052A/Guncertain significance
rs721890717:9,830,100A/Gbenign
rs5619932317:9,830,171C/Tbenign
rs1774551917:9,830,294C/Abenign
rs1085291817:9,840,501A/Gregulatory region variant
rs7545555917:9,843,216A/Gbenign
rs119395957517:9,843,515A/Guncertain significance
rs1165462017:9,846,274G/Tbenign
rs224074017:9,846,365G/Abenign
rs224074117:9,846,389G/Abenign
rs75653920617:9,846,447A/Guncertain significance
rs15041392817:9,846,520C/Tuncertain significance
rs1733949917:9,846,521G/Cbenign
rs77438604017:9,846,523T/Cuncertain significance
rs206866920517:9,846,525C/Guncertain significance
rs11190698017:9,846,527G/Abenign
rs254390777017:9,846,531C/Tuncertain significance
rs806600617:9,846,631G/Abenign
rs73380417:9,846,724A/Cbenign
rs990171517:9,850,129A/Gbenign
rs76333719117:9,850,269G/Auncertain significance
rs3490772017:9,850,286C/Tbenign
rs6206453217:9,850,440C/Tbenign
rs7653919517:9,850,479C/Gbenign
rs7789200817:9,862,999T/Cbenign
rs227768917:9,872,768A/Gbenign
rs227768817:9,872,978C/Tbenign
rs99219592717:9,873,026T/Cuncertain significance
rs14118130117:9,873,043G/Auncertain significance
rs378609417:9,875,205T/G
rs15071950517:9,885,186C/Tuncertain significance
rs378608017:9,906,554G/Aintron variant
rs3531867017:9,923,096T/Cuncertain significance
rs77458439317:9,923,121G/Auncertain significance
rs77210522117:9,923,123C/Tuncertain significance
rs76527690217:9,923,124G/Auncertain significance
rs254441635517:9,923,127C/Tuncertain significance
rs20056390517:9,923,189G/Auncertain significance
rs1293607017:10,026,855C/Tintron variant
rs1215028417:10,031,090C/G
rs991391117:10,031,183A/Gregulatory region variant
rs991425817:10,031,642C/Tregulatory region variant
rs1165669617:10,033,679C/G
rs19065787417:10,094,466T/Gintron variant
rs104303002917:10,101,650C/Tuncertain significance
rs89730061117:10,101,653G/Cuncertain significance
rs104581414617:10,101,659G/Tuncertain significance
rs117503326617:10,101,661C/Tuncertain significance
rs74615015917:10,101,697G/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.