NYAP1
neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1
Summary
Predicted to be involved in neuron projection morphogenesis and phosphatidylinositol 3-kinase/protein kinase B signal transduction. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6972167 | 7:100,080,013 | G/T | upstream gene variant | — |
| rs546810441 | 7:100,083,971 | G/A | — | — |
| rs772971384 | 7:100,084,511 | G/A | — | uncertain significance |
| rs767507827 | 7:100,084,527 | C/T | — | uncertain significance |
| rs1461380024 | 7:100,084,568 | G/A | — | uncertain significance |
| rs373386031 | 7:100,084,648 | G/A | — | uncertain significance |
| rs2131065645 | 7:100,084,710 | G/A | — | uncertain significance |
| rs369137702 | 7:100,084,766 | C/A | — | uncertain significance |
| rs181839139 | 7:100,085,210 | C/T | regulatory region variant | — |
| rs2485764002 | 7:100,085,792 | C/T | — | uncertain significance |
| rs896467588 | 7:100,085,832 | A/G | — | uncertain significance |
| rs748357526 | 7:100,085,906 | G/C | — | uncertain significance |
| rs145361652 | 7:100,085,913 | A/G | — | uncertain significance |
| rs779959857 | 7:100,085,955 | G/T | — | uncertain significance |
| rs149154346 | 7:100,086,029 | C/G | — | uncertain significance |
| rs753994861 | 7:100,086,092 | G/A | — | uncertain significance |
| rs772931629 | 7:100,086,171 | G/A | — | uncertain significance |
| rs748927970 | 7:100,086,231 | C/T | — | uncertain significance |
| rs543235608 | 7:100,086,236 | C/T | — | uncertain significance |
| rs976301402 | 7:100,086,273 | G/A | — | uncertain significance |
| rs778570072 | 7:100,086,293 | A/G | — | uncertain significance |
| rs746929783 | 7:100,086,345 | G/A | — | uncertain significance |
| rs148577061 | 7:100,086,398 | G/A | — | uncertain significance |
| rs778501741 | 7:100,086,428 | C/T | — | uncertain significance |
| rs779643944 | 7:100,086,446 | G/A | — | uncertain significance |
| rs139880279 | 7:100,086,476 | C/T | — | uncertain significance |
| rs760779356 | 7:100,086,489 | C/T | — | uncertain significance |
| rs117099690 | 7:100,086,490 | G/A | — | benign |
| rs762146711 | 7:100,086,494 | C/T | — | uncertain significance |
| rs376633711 | 7:100,086,600 | G/A | — | uncertain significance |
| rs549370649 | 7:100,086,608 | C/T | — | uncertain significance |
| rs2485766084 | 7:100,086,612 | A/C | — | uncertain significance |
| rs1328655169 | 7:100,086,651 | C/T | — | likely benign |
| rs764160440 | 7:100,086,671 | C/A | — | uncertain significance |
| rs750205490 | 7:100,086,678 | C/T | — | uncertain significance |
| rs774718976 | 7:100,086,702 | C/T | — | uncertain significance |
| rs1799751175 | 7:100,086,714 | C/T | — | uncertain significance |
| rs1425158458 | 7:100,086,836 | A/G | — | uncertain significance |
| rs779456074 | 7:100,086,882 | C/T | — | uncertain significance |
| rs780316358 | 7:100,086,887 | G/A | — | likely benign |
| rs151021245 | 7:100,086,902 | G/A | — | uncertain significance |
| rs2485766811 | 7:100,086,914 | G/T | — | uncertain significance |
| rs878860319 | 7:100,086,926 | C/T | — | uncertain significance |
| rs552035710 | 7:100,086,947 | C/T | — | uncertain significance |
| rs765270718 | 7:100,086,958 | G/A | — | likely benign |
| rs758856278 | 7:100,086,974 | C/T | — | likely benign |
| rs201640030 | 7:100,087,098 | T/C | — | uncertain significance |
| rs778518564 | 7:100,087,172 | G/A | — | uncertain significance |
| rs771007914 | 7:100,087,208 | G/C | — | uncertain significance |
| rs774500787 | 7:100,087,209 | T/G | — | uncertain significance |
| rs199625204 | 7:100,087,217 | G/A | — | likely benign |
| rs374534107 | 7:100,087,223 | T/C | — | uncertain significance |
| rs2485767676 | 7:100,087,269 | G/A | — | uncertain significance |
| rs2485767683 | 7:100,087,275 | C/G | — | uncertain significance |
| rs372379858 | 7:100,088,157 | C/T | — | uncertain significance |
| rs199612371 | 7:100,088,158 | G/A | — | uncertain significance |
| rs751138177 | 7:100,088,235 | G/T | — | uncertain significance |
| rs1233335076 | 7:100,088,287 | G/A | — | uncertain significance |
| rs551652409 | 7:100,088,305 | C/T | — | uncertain significance |
| rs145456388 | 7:100,088,313 | A/G | — | uncertain significance |
| rs371832105 | 7:100,088,615 | C/T | — | uncertain significance |
| rs2897358 | 7:100,088,640 | C/G | synonymous variant | — |
| rs149781579 | 7:100,088,653 | G/A | — | uncertain significance |
| rs138490573 | 7:100,088,698 | C/T | — | uncertain significance |
| rs7787825 | 7:100,089,385 | A/G | intron variant | — |
| rs78690606 | 7:100,090,269 | C/A | intron variant | — |
| rs765728630 | 7:100,091,274 | C/A | — | uncertain significance |
| rs758735867 | 7:100,091,279 | C/A | — | uncertain significance |
| rs1799829104 | 7:100,091,290 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.