SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2649 | snp | A/G | 0.107694 | 0.205546 | utr-variant-3-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | USP3, USP3-AS1, FBXL22 | GRCh38.p7 | 15:63594394 | ACCCACTGACGAGAC[A/G]CAGAGACCTTGGACT | 9960 |
rs10018 | snp | A/C | 0.0198 | 0.0975087 | utr-variant-3-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | USP3, USP3-AS1, FBXL22 | GRCh38.p7 | 15:63594516 | TAATCCTCTTGGCAT[A/C]ATACAAACTGGGTTT | 9960 |
rs11457 | snp | C/G | 0.45843 | 0.138046 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63594180 | GTGGGATAAGTGTAT[C/G]TAAATAGACTTATGT | 9960 |
rs289816 | snp | C/T | 0.460925 | 0.134204 | upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63502762 | TCTTCCACCCATCTC[C/T]CCATGTCAACCTATT | 9960 |
rs289817 | snp | C/T | 0.461037 | 0.134028 | upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63503476 | TTCCAAGTTGGGGCT[C/T]CTTGTAAAACCCGGC | 9960 |
rs289818 | snp | A/G | 0.461037 | 0.134028 | upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63503638 | AGGGTCAGGGATCCA[A/G]TCTCCATACAGATCA | 9960 |
rs289819 | snp | C/T | 0 | 0 | upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63504253 | AGGATACTGAACCTA[C/T]GTGGTGCGGACTACT | 9960 |
rs982077 | snp | A/G | 0.464841 | 0.127841 | intron-variant | USP3 | GRCh38.p7 | 15:63531102 | CCACTCAAAGCTTTC[A/G]TGTTCAAAACTAAAG | 9960 |
rs982078 | snp | C/G | 0.466515 | 0.124985 | intron-variant | USP3 | GRCh38.p7 | 15:63531342 | ATTGAAATAAAATTG[C/G]TAGGTTAGATACAAA | 9960 |
rs1011258 | snp | A/G | 0.459347 | 0.136653 | intron-variant | USP3 | GRCh38.p7 | 15:63545734 | catccgcccgcctta[A/G]cctcccaatgtgctg | 9960 |
rs1061848 | snp | A/C | 0 | 0 | intron-variant | USP3 | GRCh38.p7 | 15:63505458 | CCCGCAGCCTGTTTT[A/C]AAACTTCACCATCCC | 9960 |
rs1127937 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63593760 | ACACCTATTTTGAAA[A/G]CTGATCTTTTGTCCT | 9960 |
rs1136246 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63591072 | ATTTTTATAGGTAGT[G/T]GTAAGAACTTAGTCT | 9960 |
rs1421149 | snp | C/G | 0.466412 | 0.125164 | intron-variant | USP3 | GRCh38.p7 | 15:63540802 | TTAAGGAGATAAGCA[C/G]ATTAACTTGAAAATG | 9960 |
rs1421150 | snp | C/T | 0 | 0 | intron-variant | USP3 | GRCh38.p7 | 15:63540875 | GATTTCACACAAGAG[C/T]TAGTGTTTAGTTTAC | 9960 |
rs1421151 | snp | A/T | 0.466204 | 0.125522 | intron-variant, utr-variant-5-prime | USP3 | GRCh38.p7 | 15:63542120 | CATGATGTGGAAGTC[A/T]TGACTTGAGTAACTT | 9960 |
rs2011570 | snp | A/G | 0.466204 | 0.125522 | intron-variant | USP3 | GRCh38.p7 | 15:63545918 | aatggcgtgatctca[A/G]ctcactgtaacctcc | 9960 |
rs2058913 | snp | A/T | 0.459233 | 0.136827 | intron-variant | USP3 | GRCh38.p7 | 15:63539670 | TGGGGAGTATACACT[A/T]TGATGGAGTCTTCTT | 9960 |
rs2058914 | snp | A/G | 0.498009 | 0.0314867 | intron-variant | USP3 | GRCh38.p7 | 15:63539785 | GCAGCTGGTCACATT[A/G]TCGGCTCACTTGTGG | 9960 |
rs2111689 | snp | A/G | 0.483995 | 0.0880135 | intron-variant, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63525493 | TTTGGCTGCCCTCGG[A/G]CTGCCTGGGCACCTT | 9960 |
rs2160828 | snp | C/G | 0.484841 | 0.0857308 | intron-variant | USP3 | GRCh38.p7 | 15:63518986 | taaccaggatggtct[C/G]gatctcttgacctca | 9960 |
rs2414822 | snp | A/T | 0.484279 | 0.0872533 | intron-variant | USP3 | GRCh38.p7 | 15:63520285 | ctttctccaacagta[A/T]gaactggttcccatt | 9960 |
rs3210904 | snp | C/T | 0.469346 | 0.119947 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63593611 | TTTATTGGTTGGTTT[C/T]ACTTGAACAGAAACG | 9960 |
rs3751043 | snp | C/G | 0.440884 | 0.161442 | intron-variant | USP3 | GRCh38.p7 | 15:63556606 | TGGAGTTTATTCTTT[C/G]ACCTGTGGTGTAGCA | 9960 |
rs4073096 | snp | A/G | 0.457388 | 0.139608 | intron-variant | USP3 | GRCh38.p7 | 15:63547298 | AGTAGAAAAACGAAA[A/G]TTACATTCTTGAAAT | 9960 |
rs4326997 | snp | A/G | 0.157642 | 0.232314 | intron-variant | USP3 | GRCh38.p7 | 15:63573345 | GTTTTATATCTGATG[A/G]AGCAGAGGCATAAAA | 9960 |
rs4497631 | snp | A/G | 0.476574 | 0.105661 | intron-variant | USP3 | GRCh38.p7 | 15:63547309 | GAAAGTTACATTCTT[A/G]AAATAAATGTCCCTC | 9960 |
rs4556742 | snp | C/T | 0.496778 | 0.0400063 | intron-variant | USP3 | GRCh38.p7 | 15:63572234 | ATGAGTATCCATTTC[C/T]CAGAGGAAGTGATTA | 9960 |
rs4577026 | snp | A/G | 0.466204 | 0.125522 | intron-variant | USP3 | GRCh38.p7 | 15:63547294 | AAACAGTAGAAAAAC[A/G]AAAGTTACATTCTTG | 9960 |
rs4984248 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | USP3 | GRCh38.p7 | 15:63523430 | CCCGTGCTTGATACA[A/T]GTCACATGACCTGTA | 9960 |
rs4984249 | snp | A/G | 0.489837 | 0.0705577 | intron-variant | USP3 | GRCh38.p7 | 15:63557327 | GAGTGCAGTGGCACA[A/G]TCTTGGCCCATTGCA | 9960 |
rs4984250 | snp | A/T | 0.490007 | 0.0699769 | intron-variant | USP3 | GRCh38.p7 | 15:63574635 | CCTTTTTCTTCTTTG[A/T]AATACTGACTTTAAA | 9960 |
rs4984296 | snp | C/G | 0.4862 | 0.0819127 | intron-variant, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63525516 | GGCACCTTGGCAGTT[C/G]CTTCATGTAGCTTGA | 9960 |
rs4984297 | snp | G/T | 0.456214 | 0.141336 | intron-variant | USP3 | GRCh38.p7 | 15:63532291 | GACATGTGATTAAAT[G/T]ACTAGACTTAAAAAA | 9960 |
rs4984298 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | USP3 | GRCh38.p7 | 15:63550590 | aggtcatttgagaca[A/G]atatacccatagtat | 9960 |
rs4984299 | snp | C/T | 0.491834 | 0.0633738 | intron-variant | USP3 | GRCh38.p7 | 15:63557285 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 9960 |
rs4984300 | snp | C/T | 0.497668 | 0.0340657 | intron-variant | USP3 | GRCh38.p7 | 15:63557430 | ACCACGCCCGGCTAA[C/T]TTTTTCTGTTTTAGT | 9960 |
rs4984301 | snp | A/T | 0.476487 | 0.105846 | intron-variant | USP3 | GRCh38.p7 | 15:63558889 | caaaaataaataaat[A/T]aattaattaattaaa | 9960 |
rs4984302 | snp | A/G | 0.467132 | 0.12391 | intron-variant | USP3 | GRCh38.p7 | 15:63578285 | tctcaaaaacaaaga[A/G]aagaaaaaaCTTTTa | 9960 |
rs4984303 | snp | C/T | 0.459801 | 0.135955 | intron-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63589732 | TCTGTACCCCTATTA[C/T]ATGCATAGTGAATTT | 9960 |
rs6494406 | snp | A/T | 0.118235 | 0.212457 | intron-variant | USP3 | GRCh38.p7 | 15:63511590 | CGAAATTCATATTGC[A/T]TTAGTTCAGACATAA | 9960 |
rs6494407 | snp | A/G | 0.496517 | 0.0415876 | intron-variant | USP3 | GRCh38.p7 | 15:63511630 | CTCCTCACTATAGCT[A/G]TGGATAAAATGCAAT | 9960 |
rs6494408 | snp | G/T | 0.484066 | 0.0878235 | intron-variant | USP3 | GRCh38.p7 | 15:63513918 | TGTGGGAGCAACAAT[G/T]GTACAAATTGCTGGT | 9960 |
rs6494409 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | USP3 | GRCh38.p7 | 15:63517791 | GTCTGCTGTGTCCCT[A/G]TACCTAGAGCTCCTC | 9960 |
rs6494410 | snp | C/T | 0.476574 | 0.105661 | intron-variant, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63524870 | CCATATTCAGTGCGT[C/T]GGGGCAGTCACAGAG | 9960 |
rs6494411 | snp | C/T | 0.460477 | 0.134905 | intron-variant | USP3 | GRCh38.p7 | 15:63543662 | ACATGGACACATGTT[C/T]TAAAAGGTTTTAAAT | 9960 |
rs6494412 | snp | A/C | 0.489893 | 0.0703642 | intron-variant | USP3 | GRCh38.p7 | 15:63564345 | TAAGTTTATACATCT[A/C]GTGGGGTAATGACCA | 9960 |
rs6494413 | snp | A/G | 0.467439 | 0.123371 | intron-variant | USP3 | GRCh38.p7 | 15:63564443 | CCTTGAACAAGGCCC[A/G]TTAACTAATTTGATA | 9960 |
rs6494414 | snp | A/G | 0.467439 | 0.123371 | intron-variant | USP3 | GRCh38.p7 | 15:63566507 | TTTAATAGAGACGGG[A/G]TTTCACTATGTTGGC | 9960 |
rs6494415 | snp | G/T | 0.467946 | 0.122472 | intron-variant | USP3 | GRCh38.p7 | 15:63570130 | CTCTTGCTGTAGGAC[G/T]TTGGGGAAGTCACAT | 9960 |
rs6494416 | snp | G/T | 0 | 0 | intron-variant | USP3 | GRCh38.p7 | 15:63581574 | ttttttttttttttg[G/T]atttttggtatagac | 9960 |
rs6494417 | snp | C/T | 0.48995 | 0.0701706 | intron-variant | USP3 | GRCh38.p7 | 15:63581641 | acctcatgatccacc[C/T]gcctcggcctcccaa | 9960 |
rs7162745 | snp | A/T | 0.490287 | 0.0690083 | intron-variant | USP3 | GRCh38.p7 | 15:63586690 | GACTTGCTTCAGGAA[A/T]TGTAATGTCAAAATA | 9960 |
rs7163492 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | USP3 | GRCh38.p7 | 15:63528598 | TATGTGTGTGTATAT[G/T]AGTATTTCAGCTATA | 9960 |
rs7164439 | snp | A/T | | | intron-variant | USP3 | GRCh38.p7 | 15:63550191 | cgccaagctaatttt[A/T]gtatttttagaagag | 9960 |
rs7166025 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | USP3 | GRCh38.p7 | 15:63504905 | GCCGTCTAGGGGCCG[C/T]AGGCGGCCGGCGCGC | 9960 |
rs7166900 | snp | G/T | | | intron-variant | USP3 | GRCh38.p7 | 15:63505131 | TGGCCAGCTGCGTGC[G/T]CCCTTGCCCCGCCCT | 9960 |
rs7166997 | snp | C/T | 0.174288 | 0.23826 | intron-variant | USP3 | GRCh38.p7 | 15:63553979 | CATAGTTAATGGTCA[C/T]AGCTGTGCATTTATT | 9960 |
rs7168111 | snp | A/C | 0.17654 | 0.238964 | intron-variant | USP3 | GRCh38.p7 | 15:63550498 | cagatgtagagaatt[A/C]aaaaatatctacaac | 9960 |
rs7168903 | snp | A/G | 0.496616 | 0.0409947 | intron-variant | USP3 | GRCh38.p7 | 15:63581069 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATGACAGG | 9960 |
rs7171068 | snp | C/T | 0.198324 | 0.244601 | intron-variant | USP3 | GRCh38.p7 | 15:63576210 | taggctggtcttaaa[C/T]gcctaacctcaagtg | 9960 |
rs7171367 | snp | A/G | 0.105924 | 0.204309 | intron-variant | USP3 | GRCh38.p7 | 15:63576198 | tgccatgttggctag[A/G]ctggtcttaaacgcc | 9960 |
rs7171858 | snp | C/T | 0.494143 | 0.0537956 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63593500 | TACCAAATGGAACTT[C/T]AGCAACACGTTGGAC | 9960 |
rs7174587 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | USP3 | GRCh38.p7 | 15:63581646 | atgatccacctgcct[C/T]ggcctcccaaagtgc | 9960 |
rs7174884 | snp | A/G | 0.117886 | 0.21224 | intron-variant | USP3 | GRCh38.p7 | 15:63521445 | AAGATAATACTTCAA[A/G]CTATTTGTCTGCCTA | 9960 |
rs7178762 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | USP3 | GRCh38.p7 | 15:63579093 | AAAATAATCTATTCA[C/T]AGTAGCAATAAAAAC | 9960 |
rs7180729 | snp | A/T | 0.257732 | 0.24988 | intron-variant | USP3 | GRCh38.p7 | 15:63582682 | TTAAGCAACTCAAAA[A/T]GGCAGGGAGGAAGAA | 9960 |
rs7183892 | snp | C/T | 0.469346 | 0.119947 | intron-variant | USP3 | GRCh38.p7 | 15:63586733 | TCCCAGGAACCATCA[C/T]TGACATAAAATAGCA | 9960 |
rs7403729 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP3 | GRCh38.p7 | 15:63532185 | TGGGAAAACTAGGCT[C/T]AGATTTCCTAATTGT | 9960 |
rs7496126 | snp | A/G | | | intron-variant | USP3 | GRCh38.p7 | 15:63545825 | aaaatacaaaaacta[A/G]ctgggcatggtggca | 9960 |
rs7498031 | snp | A/G | | | intron-variant | USP3 | GRCh38.p7 | 15:63547745 | gagagagagagagag[A/G]gagggagggagggag | 9960 |
rs8023466 | snp | A/G | 0.26326 | 0.249648 | intron-variant | USP3 | GRCh38.p7 | 15:63549476 | tcaacgtcaaattca[A/G]aggggcatcatataa | 9960 |
rs8023506 | snp | C/T | 0.499942 | 0.00539106 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63592263 | CTCAAAGATTCAAAT[C/T]TGGAACCAGAATCCC | 9960 |
rs8025240 | snp | A/C | 0.464309 | 0.12873 | intron-variant | USP3 | GRCh38.p7 | 15:63536364 | CAGCAACTTGAGCAG[A/C]GTCTATGGCCCTGTG | 9960 |
rs8025724 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP3 | GRCh38.p7 | 15:63580380 | ATTTGTTTTAACCGA[C/T]GTGTGTCACCTTTAT | 9960 |
rs8028681 | snp | C/T | 0.468349 | 0.121752 | intron-variant | USP3 | GRCh38.p7 | 15:63572006 | AGGTGAAGGTGAGGA[C/T]GGTGGTATGGAAGAA | 9960 |
rs8029310 | snp | G/T | 0.468349 | 0.121752 | intron-variant | USP3 | GRCh38.p7 | 15:63572221 | AGCTAAAATCTTGAT[G/T]AGTATCCATTTCCCA | 9960 |
rs8031233 | snp | A/G | 0.155987 | 0.23165 | intron-variant | USP3 | GRCh38.p7 | 15:63568501 | TGACATTGCTGAAAT[A/G]TGTATACAAAACATA | 9960 |
rs8031277 | snp | C/T | 0 | 0 | intron-variant | USP3 | GRCh38.p7 | 15:63566776 | AAACACTAATTCATT[C/T]TTGTCAGTTTTGTTT | 9960 |
rs8031838 | snp | A/G | 0.105924 | 0.204309 | intron-variant | USP3 | GRCh38.p7 | 15:63560373 | gtgagccgagatcgc[A/G]ccactgccctccagc | 9960 |
rs8034068 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | USP3 | GRCh38.p7 | 15:63564354 | acatctcgtggggta[A/G]tgaccaaaattagag | 9960 |
rs8034704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP3 | GRCh38.p7 | 15:63563944 | AACTAGTGTTAACCC[C/T]AGTCTTGGTTTTGAA | 9960 |
rs8038147 | snp | C/T | 0.264906 | 0.249555 | intron-variant | USP3 | GRCh38.p7 | 15:63539533 | TATCTTTATACATTG[C/T]ATTTTAGGGGCATAT | 9960 |
rs8038912 | snp | C/T | 0.115438 | 0.210697 | intron-variant | USP3 | GRCh38.p7 | 15:63519056 | aagcgtgagccaccg[C/T]gcctggccgggtctt | 9960 |
rs8038989 | snp | A/G | 0.47666 | 0.105476 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63526208 | ATATGCCGGTATGTA[A/G]TACATACATAGACTC | 9960 |
rs8039500 | snp | A/G | 0.374 | 0.217081 | intron-variant | USP3 | GRCh38.p7 | 15:63534916 | GTTTGCCTTTTATTT[A/G]TTTATTTATTTATTT | 9960 |
rs8042222 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | USP3 | GRCh38.p7 | 15:63531854 | tgggaagctactttg[C/T]gcaaaatatacatgt | 9960 |
rs8042571 | snp | A/T | 0.00477324 | 0.0486193 | intron-variant | USP3 | GRCh38.p7 | 15:63562234 | AGAGTTTATATGCCC[A/T]GGAAAAAAATGAGCG | 9960 |
rs8043465 | snp | C/T | 0.142947 | 0.22592 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63592076 | accactacacctggc[C/T]aattttttttttgta | 9960 |
rs9672511 | snp | C/T | 0.483995 | 0.0880135 | intron-variant, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63524203 | ACAGTGGCAGCTTAG[C/T]TGAAGATAAATATCA | 9960 |
rs9673039 | snp | G/T | 0.466721 | 0.124627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63526359 | ATTTAGCAAGTTACA[G/T]TACTGCTCTGTGCCT | 9960 |
rs9744846 | snp | C/T | 0.487621 | 0.0776941 | intron-variant, upstream-variant-2KB | USP3 | GRCh38.p7 | 15:63525253 | CCCTTGAGTCCCAGG[C/T]GGCCACTTCTGACCA | 9960 |
rs10220905 | snp | C/T | | | downstream-variant-500B, intron-variant, upstream-variant-2KB | USP3, USP3-AS1, FBXL22 | GRCh38.p7 | 15:63594862 | CTCGGCCTTGCCCAG[C/T]GAAATCACCCTCAGT | 9960 |
rs10450963 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | USP3 | GRCh38.p7 | 15:63554070 | CCCAACAATTTATAA[A/G]CTACTCAATTTATTT | 9960 |
rs10450989 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | USP3 | GRCh38.p7 | 15:63554309 | AGGGGCAGTTAAATA[C/T]CAGTTGACATTACAA | 9960 |
rs11071756 | snp | C/G | 0.466412 | 0.125164 | intron-variant | USP3 | GRCh38.p7 | 15:63539437 | CTGAGGAAACTAACT[C/G]TTAAAGAAAATTTTA | 9960 |
rs11071757 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | USP3 | GRCh38.p7 | 15:63560647 | AATTTGTAGTCAACA[A/G]ATTAGTTGTGGGGGA | 9960 |
rs11071758 | snp | C/T | 0.441705 | 0.160466 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63594051 | ATTTAACACTCACCC[C/T]GGGCCAGTACACTTG | 9960 |
rs11311204 | in-del | -/T | 0.491885 | 0.0631791 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP3, USP3-AS1 | GRCh38.p7 | 15:63592334 | ACAGTCCTGTGGTGG[-/T]TTTTTTTTTTTCTTT | 9960 |
rs11321018 | in-del | -/T | | | intron-variant | USP3 | GRCh38.p7 | 15:63575159 | GTATTGTCATGATGG[-/T]TTTTTTTTTTTTTTT | 9960 |