PRAG1
PEAK1 related, kinase-activating pseudokinase 1
Summary
This gene encodes an enzyme that belongs to the tyrosine protein kinase family. A similar protein in rat binds to Rho family GTPase 2 (Rnd2) and regulates neurite outgrowth via activation of Ras homolog gene family, member A (RhoA). [provided by RefSeq, Mar 2014]
Known Variants159 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370516592 | 8:8,175,693 | G/C | — | uncertain significance |
| rs199946131 | 8:8,175,717 | C/T | — | uncertain significance |
| rs371899149 | 8:8,175,878 | G/A | — | uncertain significance |
| rs369760194 | 8:8,175,943 | G/C | — | uncertain significance |
| rs968015526 | 8:8,176,064 | C/T | — | uncertain significance |
| rs867942327 | 8:8,176,090 | G/C | — | uncertain significance |
| rs370093263 | 8:8,176,113 | A/G | — | uncertain significance |
| rs747903564 | 8:8,176,193 | C/T | — | uncertain significance |
| rs772779073 | 8:8,176,277 | T/C | — | uncertain significance |
| rs1274821532 | 8:8,176,328 | C/T | — | uncertain significance |
| rs1338471735 | 8:8,176,370 | G/A | — | uncertain significance |
| rs760984104 | 8:8,176,412 | G/A | — | uncertain significance |
| rs758208858 | 8:8,176,427 | T/A | — | uncertain significance |
| rs1585211655 | 8:8,176,442 | T/C | — | uncertain significance |
| rs376134531 | 8:8,176,472 | C/T | — | uncertain significance |
| rs1466603804 | 8:8,176,489 | C/A | — | uncertain significance |
| rs376362555 | 8:8,176,553 | G/T | — | uncertain significance |
| rs373560991 | 8:8,176,577 | C/T | — | uncertain significance |
| rs200725218 | 8:8,176,578 | G/A | — | uncertain significance |
| rs199632492 | 8:8,176,650 | G/A | — | uncertain significance |
| rs765918255 | 8:8,176,653 | G/T | — | uncertain significance |
| rs1301802634 | 8:8,176,673 | A/T | — | uncertain significance |
| rs370938903 | 8:8,176,692 | C/T | — | uncertain significance |
| rs770822750 | 8:8,176,732 | G/C | — | uncertain significance |
| rs576843455 | 8:8,176,778 | C/T | — | uncertain significance |
| rs73184312 | 8:8,179,639 | G/C | — | — |
| rs1295656543 | 8:8,185,236 | T/C | — | uncertain significance |
| rs1228540120 | 8:8,185,279 | T/C | — | uncertain significance |
| rs760046800 | 8:8,185,287 | C/A | — | uncertain significance |
| rs2486231696 | 8:8,185,331 | C/A | — | uncertain significance |
| rs753641671 | 8:8,185,342 | C/T | — | uncertain significance |
| rs554911322 | 8:8,185,345 | T/C | — | uncertain significance |
| rs778583542 | 8:8,185,403 | G/A | — | likely benign |
| rs752294490 | 8:8,185,404 | C/T | — | uncertain significance |
| rs142121457 | 8:8,185,481 | G/A | — | likely benign |
| rs751154555 | 8:8,185,528 | T/A | — | uncertain significance |
| rs1175145966 | 8:8,185,542 | G/A | — | uncertain significance |
| rs201605403 | 8:8,185,566 | T/G | — | uncertain significance |
| rs200130163 | 8:8,185,582 | C/G | — | uncertain significance |
| rs1411705561 | 8:8,185,629 | C/T | — | uncertain significance |
| rs752172969 | 8:8,185,660 | C/G | — | uncertain significance |
| rs780296797 | 8:8,185,681 | G/A | — | uncertain significance |
| rs369769327 | 8:8,185,693 | C/T | — | uncertain significance |
| rs1316297184 | 8:8,185,701 | A/G | — | likely benign |
| rs376695924 | 8:8,185,704 | G/A | — | uncertain significance |
| rs200047944 | 8:8,185,742 | C/T | — | likely benign |
| rs150737128 | 8:8,185,764 | G/A | — | uncertain significance |
| rs759862258 | 8:8,185,839 | A/G | — | uncertain significance |
| rs56207906 | 8:8,185,857 | G/A | — | uncertain significance |
| rs564201535 | 8:8,185,865 | C/A | — | uncertain significance |
| rs367674951 | 8:8,185,884 | G/T | — | uncertain significance |
| rs201115647 | 8:8,185,914 | G/A | — | uncertain significance |
| rs1453012086 | 8:8,185,923 | G/T | — | uncertain significance |
| rs768976970 | 8:8,185,974 | G/T | — | uncertain significance |
| rs200502737 | 8:8,197,000 | C/T | — | uncertain significance |
| rs200071032 | 8:8,197,104 | C/T | — | uncertain significance |
| rs370105515 | 8:8,197,133 | G/C | — | uncertain significance |
| rs1799103276 | 8:8,197,147 | G/A | — | uncertain significance |
| rs199636944 | 8:8,197,151 | C/T | — | likely benign |
| rs28454025 | 8:8,205,444 | A/G | — | — |
| rs756174151 | 8:8,233,778 | G/A | — | uncertain significance |
| rs200365497 | 8:8,233,788 | G/C | — | uncertain significance |
| rs772990903 | 8:8,233,790 | G/A | — | uncertain significance |
| rs776171034 | 8:8,233,812 | T/C | — | uncertain significance |
| rs536639997 | 8:8,233,881 | C/A | — | uncertain significance |
| rs553450708 | 8:8,233,908 | G/T | — | uncertain significance |
| rs781168064 | 8:8,233,917 | T/C | — | uncertain significance |
| rs376370871 | 8:8,233,919 | G/A | — | uncertain significance |
| rs1206328980 | 8:8,233,950 | T/C | — | likely benign |
| rs2486346687 | 8:8,233,993 | C/G | — | uncertain significance |
| rs778245704 | 8:8,234,012 | C/T | — | uncertain significance |
| rs368407767 | 8:8,234,052 | G/A | — | uncertain significance |
| rs577867675 | 8:8,234,054 | C/T | — | uncertain significance |
| rs375961403 | 8:8,234,070 | A/T | — | uncertain significance |
| rs761974439 | 8:8,234,078 | G/A | — | likely benign |
| rs984025835 | 8:8,234,109 | T/C | — | uncertain significance |
| rs369067268 | 8:8,234,112 | C/T | — | likely benign |
| rs199706360 | 8:8,234,126 | C/T | — | uncertain significance |
| rs776366489 | 8:8,234,130 | A/C | — | uncertain significance |
| rs1490496941 | 8:8,234,171 | G/A | — | uncertain significance |
| rs1326194505 | 8:8,234,198 | C/A | — | uncertain significance |
| rs199654083 | 8:8,234,200 | A/G | — | likely benign |
| rs765679055 | 8:8,234,220 | G/A | — | uncertain significance |
| rs752826886 | 8:8,234,226 | C/T | — | uncertain significance |
| rs200846210 | 8:8,234,246 | G/A | — | uncertain significance |
| rs773878783 | 8:8,234,258 | G/C | — | uncertain significance |
| rs202019835 | 8:8,234,319 | T/G | — | uncertain significance |
| rs775930768 | 8:8,234,322 | C/T | — | uncertain significance |
| rs565227789 | 8:8,234,351 | G/C | — | uncertain significance |
| rs762443182 | 8:8,234,390 | A/G | — | likely benign |
| rs2486348424 | 8:8,234,392 | C/G | — | uncertain significance |
| rs2486348449 | 8:8,234,399 | T/A | — | uncertain significance |
| rs752480564 | 8:8,234,400 | T/G | — | uncertain significance |
| rs2486348744 | 8:8,234,463 | T/C | — | uncertain significance |
| rs1182540362 | 8:8,234,487 | G/A | — | uncertain significance |
| rs750946451 | 8:8,234,496 | T/G | — | uncertain significance |
| rs552652315 | 8:8,234,543 | C/A | — | uncertain significance |
| rs760279552 | 8:8,234,577 | C/T | — | likely benign |
| rs1158570733 | 8:8,234,597 | C/T | — | uncertain significance |
| rs1250939720 | 8:8,234,616 | C/A | — | uncertain significance |
Showing 100 of 159 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.