SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1004649 | snp | G/T | 0.146314 | 0.227484 | intron-variant | WRAP73 | GRCh38.p7 | 1:3649869 | GGCCGCCCCCGGCCC[G/T]GCCCGCCGGGGACGC | 49856 |
rs1004650 | snp | A/C | 0.13446 | 0.221699 | upstream-variant-2KB | TP73, WRAP73 | GRCh38.p7 | 1:3651598 | TCTACCGGCCAGCGA[A/C]ACCCGCCGCCCCGCC | 49856 |
rs1046926 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3630965 | ACGTAGCAGCGGTGC[A/C]CTAACGTGTGCAGAA | 49856 |
rs1885864 | snp | A/G | 0.318415 | 0.240457 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638424 | AGACCCCTTCCAGCC[A/G]ATGCCTGTTGAGAGG | 49856 |
rs2181485 | snp | C/T | 0.356597 | 0.226135 | intron-variant | WRAP73 | GRCh38.p7 | 1:3631778 | ACTGCAGGGTGCAGC[C/T]GCCCCACCCCACCGG | 49856 |
rs2244942 | snp | A/G | 0.491473 | 0.0647364 | intron-variant | WRAP73 | GRCh38.p7 | 1:3631978 | CTGCTCACTTGCTCC[A/G]CTCTGCTGAGTAGAA | 49856 |
rs2251098 | snp | C/T | 0.41408 | 0.188621 | upstream-variant-2KB | WRAP73 | GRCh38.p7 | 1:3650142 | AATGCCGCGCGGAAG[C/T]CGGCGGCGCTGATAG | 49856 |
rs2273954 | snp | C/T | 0.489024 | 0.0732638 | intron-variant | WRAP73 | GRCh38.p7 | 1:3633288 | AAAAACTTTTTTTCC[C/T]TTCCATGCTTCCAGC | 49856 |
rs2281710 | snp | A/G | | | intron-variant, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3632056 | CACAGAAGCTCCTTG[A/G]AGGCGCTGGGCCTTT | 49856 |
rs2296034 | snp | C/T | 0.136317 | 0.222657 | synonymous-codon, intron-variant, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3635228 | GCTTACGAGTGGTCC[C/T]TGGGCATCAAGTCTG | 49856 |
rs2760317 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | WRAP73 | GRCh38.p7 | 1:3639892 | CTTACGCTGCTGGAG[A/G]CGGTCCCCCACCCCG | 49856 |
rs2760318 | snp | A/C | 0.0930568 | 0.194599 | intron-variant | WRAP73 | GRCh38.p7 | 1:3639306 | GCAGGAGGCAGACGG[A/C]CACCTTCTTGGGTGT | 49856 |
rs2760319 | snp | C/T | 0.238749 | 0.249747 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638060 | CATTTGAATGCAATG[C/T]AGTCACACTCTTATT | 49856 |
rs2760320 | snp | C/G | 0.125523 | 0.216808 | missense, intron-variant | WRAP73 | GRCh38.p7 | 1:3632268 | AGCAAACCCGAAAAT[C/G]GGCATAGGAATGCTG | 49856 |
rs2760321 | snp | A/G | 0.222209 | 0.24845 | synonymous-codon, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3631572 | GTCCCCAGTGCGCGC[A/G]TTTCAGTGGGACCCG | 49856 |
rs2821007 | snp | C/T | 0.093777 | 0.195178 | downstream-variant-500B | WRAP73, TPRG1L | GRCh38.p7 | 1:3630371 | AGGAAGTGCCTAGAA[C/T]CACCCAGAACCATTC | 49856 |
rs2821032 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | WRAP73 | GRCh38.p7 | 1:3640342 | TGAGTCTGAGAGGCT[C/T]GGGCAAGGTTTCAGC | 49856 |
rs2821058 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637225 | GGAGCAGTGCTCGGC[A/G]TTGTGCCATTTCCCT | 49856 |
rs2821061 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | WRAP73 | GRCh38.p7 | 1:3636216 | GCACTGACGCTGGCA[C/T]CTGTGGCGGTGCAGC | 49856 |
rs2821071 | snp | C/T | 0.084364 | 0.187256 | intron-variant | WRAP73 | GRCh38.p7 | 1:3631885 | AAAAAAAAAAAAAAA[C/T]ACCAAAGAAAGAAAC | 49856 |
rs3765689 | snp | A/G | 0.146314 | 0.227484 | intron-variant | WRAP73 | GRCh38.p7 | 1:3642918 | ACGCAAACTAAATCC[A/G]AACTGCAGTATCATT | 49856 |
rs3765690 | snp | A/T | 0.232943 | 0.249417 | intron-variant | WRAP73 | GRCh38.p7 | 1:3648254 | AAACAATTTCAAGTA[A/T]AAATAACGCCTGAGT | 49856 |
rs3818330 | snp | A/C | 0.339684 | 0.233369 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638864 | CGGTCTCTGATGATG[A/C]TAAAGAAGTGTTTCC | 49856 |
rs6686644 | snp | A/G | 0.119281 | 0.213102 | intron-variant | WRAP73 | GRCh38.p7 | 1:3644434 | CCTAGTGGCCCCGCT[A/G]ATCCTCGAACGGGTC | 49856 |
rs7517179 | snp | A/G | 0.120326 | 0.21374 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641631 | CACGAGGAGCCCCAT[A/G]CCACGGGCGAACAGT | 49856 |
rs7519550 | snp | A/G | 0.122411 | 0.214991 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641698 | GACTCACTCAACTGT[A/G]CTCTTAAAGTGGGTG | 49856 |
rs7526126 | snp | C/G | 0.234692 | 0.249531 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641557 | GTAGGCAGTGCTGCT[C/G]GCCCCGCAGCAGGCA | 49856 |
rs7526179 | snp | C/T | 0.160938 | 0.233598 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641567 | CTGCTCGCCCCGCAG[C/T]AGGCACCGGCTGCCG | 49856 |
rs7528494 | snp | C/T | 0.120326 | 0.21374 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641664 | TGGTCCTGATTGTGG[C/T]GGCAATGACGTGCAA | 49856 |
rs7537171 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | WRAP73 | GRCh38.p7 | 1:3649715 | CCCCGGGCCCTCCAC[C/T]TGTCTAGGGTATCTT | 49856 |
rs10909993 | snp | A/G | 0.147991 | 0.228242 | intron-variant | WRAP73 | GRCh38.p7 | 1:3632466 | AGGGGAGGAAAGTGC[A/G]GCCCAAGGGCAGGAA | 49856 |
rs10909994 | snp | A/G | 0.154993 | 0.231244 | intron-variant | WRAP73 | GRCh38.p7 | 1:3632633 | GGACAGGTCCTAGCT[A/G]CAATCTCAGCAGCTC | 49856 |
rs10909996 | snp | A/G | 0.121717 | 0.214577 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637671 | acttggtgaaacccc[A/G]tctctacaaaatatc | 49856 |
rs10909997 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637834 | gcaagaccctgtctc[A/T]aaaaaGTAATAATAA | 49856 |
rs10909998 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638025 | CTCATCTGGAGGGAC[A/G]CTAATATTCCAACTA | 49856 |
rs10909999 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638527 | GTTGTCTTGAGTCAC[C/T]GTGGTCATGTTTTAA | 49856 |
rs10910000 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | WRAP73 | GRCh38.p7 | 1:3644694 | ATGACCTTAGTCTTA[A/G]GTTGAACAATGTCAT | 49856 |
rs11586067 | snp | A/G | 0.00472811 | 0.0483911 | intron-variant | WRAP73 | GRCh38.p7 | 1:3649139 | AGGACATACATACTA[A/G]GCATCCGGGTTATCC | 49856 |
rs12036402 | snp | C/G | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3640407 | CAGCAGGGCGGGGTG[C/G]AGCGCCCGAGCATCT | 49856 |
rs12036448 | snp | A/G | 0 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3640512 | GAGCATCAGCAGGGC[A/G]GGGTGCAGCGCCCGA | 49856 |
rs12038064 | snp | C/T | 0.315516 | 0.241263 | intron-variant | WRAP73 | GRCh38.p7 | 1:3639108 | GCTTTTTCAAAGTGA[C/T]CATAGGTTGCATGTT | 49856 |
rs12040481 | snp | A/G | 0.5 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3640475 | GAGCATCAGCAGGGC[A/G]GGGTGGAACACCCGA | 49856 |
rs12040483 | snp | A/G | 0 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3640483 | GCAGGGCAGGGTGGA[A/G]CACCCGAGGCTCTGA | 49856 |
rs12040484 | snp | A/G | 0 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3640485 | AGGGCAGGGTGGAAC[A/G]CCCGAGGCTCTGAGC | 49856 |
rs12040834 | snp | G/T | 0 | 0 | synonymous-codon, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3649961 | CGGGGAGAACTTGCA[G/T]AGTAAGCTGGAGAGC | 49856 |
rs12043953 | snp | A/C | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3645398 | gcgcagcgggacggg[A/C]gggttgccccgtggt | 49856 |
rs12043954 | snp | A/C | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3645417 | ttgccccgtggtgtg[A/C]gcggcgcagcgggac | 49856 |
rs12043956 | snp | C/G | 0.375 | 0.216506 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645458 | ccccgtggtgtgcgc[C/G]gtgcagcgggacggg | 49856 |
rs12046309 | snp | C/T | 0.404559 | 0.196498 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645356 | AGCGGCGCAGCGGGA[C/T]GGGCGGGTTGCCCCG | 49856 |
rs12046328 | snp | C/T | 0.347914 | 0.230028 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645381 | GCCCCGTGGTGTgcg[C/T]ggcgcagcgggacgg | 49856 |
rs12046332 | snp | C/T | 0.375 | 0.216506 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645460 | ccgtggtgtgcgccg[C/T]gcagcgggacgggcg | 49856 |
rs12077454 | snp | A/G/T | 0.0752113 | 0.178743 | intron-variant | WRAP73 | GRCh38.p7 | 1:3639503 | TGAGGGAGAGGCACC[A/G/T]CAGTGGGTGGTCCAG | 49856 |
rs12078530 | snp | C/T | 0.121369 | 0.214369 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637264 | ACAAGAACATTCTAG[C/T]GCAGAGGAGAAACCC | 49856 |
rs12078536 | snp | C/G | 0.120674 | 0.21395 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637291 | ACCCAAGGCACGGTG[C/G]CTTCACCCTCACAAC | 49856 |
rs12078583 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WRAP73 | GRCh38.p7 | 1:3637425 | AGAAACACAGGCCTT[C/T]GAGTCCCCCCATGTC | 49856 |
rs12079436 | snp | A/G | 0.154993 | 0.231244 | intron-variant | WRAP73 | GRCh38.p7 | 1:3631205 | CCTGCAGGCCAGCAC[A/G]GTGCCTGGAGTGACC | 49856 |
rs12084349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641429 | CTCAAGATGGAGGAA[C/T]GGGCCACTGATCCAC | 49856 |
rs12085065 | snp | A/C | 0.185788 | 0.241613 | intron-variant | WRAP73 | GRCh38.p7 | 1:3634744 | AGACCACAAAGGAGA[A/C]AACTGGACTGGGGTG | 49856 |
rs12086188 | snp | C/G | 0 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645534 | ccccgtggtgtgcgc[C/G]gcgcagcgGGATGGG | 49856 |
rs12086552 | snp | C/G | 0.275999 | 0.248644 | intron-variant | WRAP73 | GRCh38.p7 | 1:3647667 | GGCCTTCTCTCCTGC[C/G]AGAGGTTTCATGTCT | 49856 |
rs12087237 | snp | A/G | 0.131381 | 0.220067 | intron-variant | WRAP73 | GRCh38.p7 | 1:3646950 | TCCCTTAAAACCAGC[A/G]GAGACCCGATCACAC | 49856 |
rs12090129 | snp | C/T | 0 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645536 | ccgtggtgtgcgcgg[C/T]gcagcgGGATGGGCG | 49856 |
rs12093478 | snp | C/T | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3645546 | cgcggcgcagcgGGA[C/T]GGGCGGGTTACCGAG | 49856 |
rs12134253 | snp | G/T | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3637315 | TCACAACGCAGTGTG[G/T]GCTGGGGGAAGCTGT | 49856 |
rs12137667 | snp | A/T | 0.00491036 | 0.0493059 | intron-variant | WRAP73 | GRCh38.p7 | 1:3636078 | GGAAAATATTTTCGT[A/T]AATAAATAATTGCAT | 49856 |
rs12408890 | snp | C/T | 0.499424 | 0.0169631 | intron-variant | WRAP73 | GRCh38.p7 | 1:3644444 | CCGCTAATCCTCGAA[C/T]GGGTCTGGTCCTTGC | 49856 |
rs12565918 | snp | A/G/T | 6.77782e-05 | 0.00582104 | missense, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3631579 | CACTGAAATGCGCGC[A/G/T]CTGGGGACAGCTGCT | 49856 |
rs12730278 | snp | C/T | 0.282895 | 0.247826 | intron-variant | WRAP73 | GRCh38.p7 | 1:3645432 | cgcggcgcagcggga[C/T]gggcgggttgccccg | 49856 |
rs12730382 | snp | C/T | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3645470 | cgccgtgcagcggga[C/T]gggcgggttgccccg | 49856 |
rs12737240 | snp | C/T | 0.5 | 0 | intron-variant | WRAP73 | GRCh38.p7 | 1:3644368 | GCCTTCGGAAGGGGA[C/T]CCAGTGGCCCCGCTG | 49856 |
rs12737247 | snp | C/T | 0.375 | 0.216506 | intron-variant | WRAP73 | GRCh38.p7 | 1:3644373 | CGGAAGGGGATCCAG[C/T]GGCCCCGCTGAGCCC | 49856 |
rs12754811 | snp | A/G | 0.00961516 | 0.0686668 | intron-variant | WRAP73 | GRCh38.p7 | 1:3632937 | CCCTCATGCCCCTGT[A/G]GGATGGGTGCTTTTA | 49856 |
rs16823940 | snp | C/T | 0.0168648 | 0.0902661 | missense, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3631634 | TCTGAATGTCCCAGA[C/T]CCAGACGGCATTGGG | 49856 |
rs28413094 | snp | C/T | | | missense, nc-transcript-variant | WRAP73 | GRCh38.p7 | 1:3635945 | GGTCATCTTCATACC[C/T]CCAAGCAGGTGTCCC | 49856 |
rs28446481 | snp | A/C | 0.0414274 | 0.137843 | intron-variant | WRAP73 | GRCh38.p7 | 1:3635334 | TAATGAATACACCCC[A/C]GTCGCCAGGAACACA | 49856 |
rs28503229 | snp | A/G | 0.0459104 | 0.144386 | intron-variant | WRAP73 | GRCh38.p7 | 1:3635341 | TACACCCCCGTCGCC[A/G]GGAACACACCACAGA | 49856 |
rs34086330 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WRAP73 | GRCh38.p7 | 1:3634660 | GTGCCTGGCACGACA[A/G]CAGATGCCCAGTGTT | 49856 |
rs34188120 | in-del | -/G | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3632865 | CACACACCGAGCCCC[-/G]GGGGTGGGCCCGTCG | 49856 |
rs34461044 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641358 | TCAAGACGGGAGGAA[C/G]AGGCCACTGATCCAT | 49856 |
rs34514629 | in-del | -/C | 0.499551 | 0.0149693 | intron-variant | WRAP73 | GRCh38.p7 | 1:3646949 | CTCCCTTAAAACCAG[-/C]AGAGACCCGATCACA | 49856 |
rs34620425 | in-del | -/C | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3635621 | ACACAGAAGTTCAAG[-/C]AGCAGTCTGGGCAAC | 49856 |
rs34879094 | in-del | -/A | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3642401 | CTGCAGGTATAATGG[-/A]AACTGAGCTCCTGCT | 49856 |
rs34946124 | snp | C/G | 0.32627 | 0.238082 | downstream-variant-500B | WRAP73, TPRG1L | GRCh38.p7 | 1:3630473 | CTGACTCAGCTGGTC[C/G]GGGACCTGCAGCTCC | 49856 |
rs35166074 | in-del | -/C | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3633960 | GTGGAAGGCGGGCAG[-/C]CCCTACGCCCCTGAA | 49856 |
rs35197479 | in-del | -/C | 0.154993 | 0.231244 | intron-variant | WRAP73 | GRCh38.p7 | 1:3632530 | GCCTGCCCGCAAGTG[-/C]CCCGGATGAGAGTGG | 49856 |
rs35260794 | snp | C/T | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3645508 | CGCGGCGCAGCGGGA[C/T]GGGCGGGTTGCCCCG | 49856 |
rs35447644 | in-del | -/G | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3635578 | TAATCCCAGCACTTT[-/G]GGGAGGCCGAAGCTG | 49856 |
rs35627483 | in-del | -/A | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3638147 | TATGTTTCATTCCGC[-/A]AAAAGACAGTGCGGT | 49856 |
rs35743795 | in-del | -/A | 0.492871 | 0.0592773 | intron-variant | WRAP73 | GRCh38.p7 | 1:3642756 | AAAAAAAAAAAAAAA[-/A]TGCTGCTGGGAAAAG | 49856 |
rs35759879 | in-del | -/T | | | frameshift-variant, intron-variant | WRAP73 | GRCh38.p7 | 1:3632270 | GCATTCCTATGCCGA[-/T]TTTCGGGTTTGCTCT | 49856 |
rs35798495 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WRAP73 | GRCh38.p7 | 1:3642449 | CCTTCTAAATAAATG[C/T]TGCTGGGAGCTGGGC | 49856 |
rs35863450 | in-del | -/AA | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3638373 | ATATTTAGTCCACAG[-/AA]GAGAGAAAGCTCAGA | 49856 |
rs35905873 | in-del | -/G | | | intron-variant | WRAP73 | GRCh38.p7 | 1:3631451 | CACGTCCGTGGCCTC[-/G]GGGGATGTGCTTACC | 49856 |
rs56101886 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WRAP73 | GRCh38.p7 | 1:3647272 | TTAAACTTTAGAGAA[C/T]GTTATAATTTCAAAA | 49856 |
rs56280155 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WRAP73 | GRCh38.p7 | 1:3643055 | TATGTGCCCAGGAGA[C/T]GGGGACAACACGTTC | 49856 |
rs56354975 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | WRAP73 | GRCh38.p7 | 1:3649722 | CCCTCCACCTGTCTA[G/T]GGTATCTTCCTGGGT | 49856 |
rs57595901 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638906 | AACCCGCCCACGCGT[C/T]CCCAAGCACAGGCCT | 49856 |
rs58080962 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | WRAP73 | GRCh38.p7 | 1:3648607 | TGAAAACTAGAAACA[G/T]GGACCTGCTCTCCCC | 49856 |
rs58320352 | in-del | -/AAAA | 0.0490535 | 0.14873 | intron-variant | WRAP73 | GRCh38.p7 | 1:3641762 | TTATTCAGATATAAG[-/AAAA]AGTCTGCAGTCTGGA | 49856 |
rs58651937 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | WRAP73 | GRCh38.p7 | 1:3638204 | TCCCACTAGCTCTGC[A/G]CGGTCCAGTTAGACG | 49856 |