PRR14L
proline rich 14 like
Known Variants147 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1285063026 | 22:32,081,650 | C/G | — | uncertain significance |
| rs78356740 | 22:32,081,684 | G/A | — | benign |
| rs55728055 | 22:32,093,268 | G/C | intron variant | — |
| rs2523585742 | 22:32,097,663 | A/G | — | uncertain significance |
| rs2523587971 | 22:32,099,586 | C/T | — | uncertain significance |
| rs2523587996 | 22:32,099,594 | A/C | — | uncertain significance |
| rs2523588006 | 22:32,099,598 | C/T | — | uncertain significance |
| rs757306550 | 22:32,099,610 | G/A | — | uncertain significance |
| rs2523588052 | 22:32,099,613 | C/T | — | uncertain significance |
| rs751436496 | 22:32,099,684 | A/C | — | uncertain significance |
| rs146983374 | 22:32,100,678 | T/C | — | uncertain significance |
| rs138055187 | 22:32,100,705 | T/C | — | uncertain significance |
| rs1400754822 | 22:32,108,090 | G/T | — | uncertain significance |
| rs374479009 | 22:32,108,097 | G/A | — | uncertain significance |
| rs776457027 | 22:32,108,219 | A/G | — | uncertain significance |
| rs143043548 | 22:32,108,234 | C/T | — | uncertain significance |
| rs751253317 | 22:32,108,235 | G/A | — | uncertain significance |
| rs753079943 | 22:32,108,286 | T/C | — | uncertain significance |
| rs781387974 | 22:32,108,297 | C/T | — | conflicting classifications of pathogenicity |
| rs116362217 | 22:32,108,345 | C/T | — | benign |
| rs535257671 | 22:32,108,514 | C/T | — | uncertain significance |
| rs2517565464 | 22:32,108,579 | A/G | — | uncertain significance |
| rs2517565619 | 22:32,108,708 | T/C | — | uncertain significance |
| rs542558036 | 22:32,108,739 | T/C | — | uncertain significance |
| rs2517565686 | 22:32,108,765 | G/T | — | uncertain significance |
| rs114057802 | 22:32,108,838 | A/G | — | benign |
| rs2517565767 | 22:32,108,840 | C/T | — | uncertain significance |
| rs988329229 | 22:32,108,856 | T/C | — | uncertain significance |
| rs1480056361 | 22:32,108,870 | T/C | — | uncertain significance |
| rs2074632107 | 22:32,108,915 | T/G | — | uncertain significance |
| rs2074632120 | 22:32,108,917 | T/G | — | uncertain significance |
| rs1000652723 | 22:32,108,921 | A/C | — | uncertain significance |
| rs2074632164 | 22:32,108,924 | T/G | — | uncertain significance |
| rs199620955 | 22:32,108,951 | T/A | — | uncertain significance |
| rs2517565961 | 22:32,108,985 | C/T | — | uncertain significance |
| rs759920962 | 22:32,109,183 | C/T | — | uncertain significance |
| rs1049636101 | 22:32,109,315 | C/A | — | uncertain significance |
| rs941204126 | 22:32,109,357 | C/T | — | uncertain significance |
| rs1437468369 | 22:32,109,362 | A/C | — | uncertain significance |
| rs751560910 | 22:32,109,377 | C/A | — | uncertain significance |
| rs180740203 | 22:32,109,497 | A/G | — | uncertain significance |
| rs2517566666 | 22:32,109,528 | G/C | — | uncertain significance |
| rs2517566691 | 22:32,109,553 | C/G | — | likely benign |
| rs556459687 | 22:32,109,554 | A/G | — | uncertain significance |
| rs967791904 | 22:32,109,609 | T/C | — | uncertain significance |
| rs1438460273 | 22:32,109,651 | G/A | — | uncertain significance |
| rs1210868113 | 22:32,109,652 | G/T | — | uncertain significance |
| rs560126282 | 22:32,109,672 | G/A | — | uncertain significance |
| rs144157513 | 22:32,109,726 | C/T | — | uncertain significance |
| rs1480711139 | 22:32,109,731 | T/A | — | uncertain significance |
| rs1043361528 | 22:32,109,767 | T/C | — | uncertain significance |
| rs574937663 | 22:32,109,788 | A/G | — | uncertain significance |
| rs147362639 | 22:32,109,791 | C/T | — | uncertain significance |
| rs572612867 | 22:32,109,888 | G/C | — | uncertain significance |
| rs367563131 | 22:32,109,895 | T/A | — | uncertain significance |
| rs115688748 | 22:32,109,927 | C/T | — | benign |
| rs2074638971 | 22:32,109,952 | C/A | — | uncertain significance |
| rs776494925 | 22:32,110,190 | C/T | — | likely benign |
| rs2517567672 | 22:32,110,243 | T/G | — | uncertain significance |
| rs1017894504 | 22:32,110,327 | T/C | — | likely benign |
| rs2517567819 | 22:32,110,394 | T/C | — | uncertain significance |
| rs547919067 | 22:32,110,416 | A/T | — | uncertain significance |
| rs866207796 | 22:32,110,419 | C/T | — | likely benign |
| rs1449156614 | 22:32,110,421 | T/C | — | uncertain significance |
| rs2517567968 | 22:32,110,497 | C/A | — | uncertain significance |
| rs748228992 | 22:32,110,509 | T/C | — | uncertain significance |
| rs1455182897 | 22:32,110,511 | T/A | — | uncertain significance |
| rs543103538 | 22:32,110,532 | C/T | — | likely benign |
| rs144955642 | 22:32,110,614 | C/T | — | uncertain significance |
| rs775687504 | 22:32,110,634 | A/C | — | uncertain significance |
| rs889870850 | 22:32,110,701 | T/C | — | uncertain significance |
| rs1376095689 | 22:32,110,707 | C/A | — | uncertain significance |
| rs768712544 | 22:32,110,712 | G/C | — | uncertain significance |
| rs769686260 | 22:32,110,844 | C/A | — | uncertain significance |
| rs1293176702 | 22:32,110,908 | G/C | — | uncertain significance |
| rs9619227 | 22:32,110,938 | C/T | — | benign |
| rs752401014 | 22:32,110,971 | T/C | — | uncertain significance |
| rs932974213 | 22:32,110,979 | A/G | — | uncertain significance |
| rs886163621 | 22:32,110,997 | T/C | — | uncertain significance |
| rs1038238428 | 22:32,111,019 | G/T | — | uncertain significance |
| rs770161725 | 22:32,111,060 | G/A | — | uncertain significance |
| rs2517568915 | 22:32,111,135 | T/C | — | uncertain significance |
| rs1277981137 | 22:32,111,169 | A/G | — | uncertain significance |
| rs1169959982 | 22:32,111,211 | T/C | — | uncertain significance |
| rs1295480581 | 22:32,111,335 | G/T | — | uncertain significance |
| rs200364483 | 22:32,111,362 | T/C | — | uncertain significance |
| rs573653422 | 22:32,111,412 | C/T | — | uncertain significance |
| rs1035369924 | 22:32,111,414 | G/C | — | likely benign |
| rs2074652156 | 22:32,111,474 | T/A | — | uncertain significance |
| rs2517569461 | 22:32,111,496 | A/C | — | uncertain significance |
| rs766174090 | 22:32,111,549 | C/G | — | uncertain significance |
| rs2517569642 | 22:32,111,625 | T/A | — | uncertain significance |
| rs1057287250 | 22:32,111,679 | T/C | — | uncertain significance |
| rs2517569732 | 22:32,111,685 | T/C | — | uncertain significance |
| rs1250543801 | 22:32,111,693 | G/C | — | uncertain significance |
| rs868325588 | 22:32,111,703 | G/T | — | uncertain significance |
| rs1251335203 | 22:32,111,706 | T/C | — | uncertain significance |
| rs766505915 | 22:32,111,714 | A/T | — | uncertain significance |
| rs1350389467 | 22:32,111,727 | C/T | — | uncertain significance |
| rs756997972 | 22:32,111,816 | G/T | — | uncertain significance |
Showing 100 of 147 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.