SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs747423 | snp | C/T | 0.310386 | 0.242597 | intron-variant | USP36 | GRCh38.p7 | 17:78788699 | AGATGTGGAGGGACT[C/T]GGGTCCATGGGGTAG | 57602 |
rs867596 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | USP36 | GRCh38.p7 | 17:78795135 | GTCTGAAGGCATTTG[C/T]GTTGTAGCCTGGGCA | 57602 |
rs900348 | snp | G/T | 0.322721 | 0.23919 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837347 | CCCACTCTCCTGCTT[G/T]GCTTTTCTTCTTCTC | 57602 |
rs900349 | snp | A/G | 0.492435 | 0.0610346 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836051 | TGACGAAGTGGATGG[A/G]CTTAAATATTGACTA | 57602 |
rs931226 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP36 | GRCh38.p7 | 17:78824498 | agagtgcagtggtgc[A/G]atctccgctcacggc | 57602 |
rs1044486 | snp | C/T | 0.442113 | 0.159977 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796097 | ACATACATTCGTTAA[C/T]TCTTGGGCAGTGGTG | 57602 |
rs1057040 | snp | C/T | 0.499029 | 0.0220079 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803713 | CTGGGCTCAGAGACG[C/T]GCCTCCCACAGCACA | 57602 |
rs1108430 | snp | A/G | 0.128632 | 0.218563 | intron-variant | USP36 | GRCh38.p7 | 17:78792617 | caactggtgttttaa[A/G]gagcccctggcaatt | 57602 |
rs1110274 | snp | G/T | 0.493703 | 0.0557558 | intron-variant | USP36 | GRCh38.p7 | 17:78814202 | TTCTCAGACTTGCAG[G/T]GAGACACGGAAGAGG | 57602 |
rs1317718 | snp | A/G | 0.361684 | 0.223667 | intron-variant | USP36 | GRCh38.p7 | 17:78789158 | CCAGGCTGGGGTGCA[A/G]TGGCGCAATCTCGAC | 57602 |
rs1531797 | snp | A/G | 0.439085 | 0.163545 | intron-variant | USP36 | GRCh38.p7 | 17:78826086 | CCAGGTCTGCCCTTC[A/G]GTGAACTGGGTAATT | 57602 |
rs1531798 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | USP36 | GRCh38.p7 | 17:78826049 | CTGTTCCCTGTGTGC[C/T]GGGCCCCATAGCTAG | 57602 |
rs2054623 | snp | A/G | 0.00872282 | 0.0654624 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807148 | GAGATGGGCCGCTCC[A/G]CTCCTGGGGGTCTGG | 57602 |
rs2054624 | snp | C/T | 0.237593 | 0.249692 | intron-variant | USP36 | GRCh38.p7 | 17:78806016 | GATCTTGGTCAGTGA[C/T]GCCCCCCTGTACCTC | 57602 |
rs2277701 | snp | G/T | 0.0539704 | 0.155153 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840779 | CGGGCCGAAGGAGTC[G/T]CCAGGGCTGCGTAGG | 57602 |
rs2277702 | snp | C/T | 0.117537 | 0.212022 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840488 | GCCGGGCTGTCCTCG[C/T]CGGTCTCCGCCGTCC | 57602 |
rs2277703 | snp | C/G | 0.183886 | 0.241099 | intron-variant | USP36 | GRCh38.p7 | 17:78838839 | TCGTGGTAGAGGGTT[C/G]CCGGTGCGCGCCGCA | 57602 |
rs2277704 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838678 | TACATTCAGGAGCTC[C/T]GCGTAGCACCTGCCC | 57602 |
rs2279308 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | USP36 | GRCh38.p7 | 17:78798899 | AGGGAAGGTATGATG[C/T]GTGATGCTGACCACA | 57602 |
rs2279309 | snp | A/G | 0.167158 | 0.235875 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796751 | TAAGTCCAACACCAC[A/G]TTGTCCATCTCCACC | 57602 |
rs2279310 | snp | C/T | 0.182933 | 0.240836 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796788 | GACTCCGGGAGGAAA[C/T]GACGGGGACAGACCC | 57602 |
rs2306525 | snp | A/G | 0.0153263 | 0.0861874 | intron-variant | USP36 | GRCh38.p7 | 17:78802289 | GTGGGAACCGCATGG[A/G]TGTGCACCGGGCGAG | 57602 |
rs2306526 | snp | A/G | 0.496235 | 0.0432229 | intron-variant | USP36 | GRCh38.p7 | 17:78802280 | GCATGGGTGTGCACC[A/G]GGCGAGGGGTTGGGG | 57602 |
rs2306527 | snp | A/G | 0.476833 | 0.105105 | intron-variant | USP36 | GRCh38.p7 | 17:78802073 | GCGTGGGTGTGCACC[A/G]GGTGAGGGGGTATTG | 57602 |
rs2376827 | snp | C/T | 0.181659 | 0.240478 | intron-variant | USP36 | GRCh38.p7 | 17:78788217 | GTCGCCAGGCTGGAG[C/T]GCAGTGGTGCAATCT | 57602 |
rs2376828 | snp | C/T | 0.453331 | 0.145452 | intron-variant | USP36 | GRCh38.p7 | 17:78816758 | ctgacattagagttg[C/T]gagccattgtgccca | 57602 |
rs2376829 | snp | C/T | 0.448452 | 0.152042 | intron-variant | USP36 | GRCh38.p7 | 17:78817043 | ccacatatacaacag[C/T]gatcccataagatta | 57602 |
rs2889479 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | USP36 | GRCh38.p7 | 17:78788116 | caggaagcgagtaca[C/T]GAAGCTCTGCAAGTT | 57602 |
rs3068285 | in-del | -/G | 0.496314 | 0.0427728 | intron-variant | USP36 | GRCh38.p7 | 17:78813270 | CACCAGAAAGCAAGA[-/G]ACCTCAAACACCTCA | 57602 |
rs3068286 | in-del | -/CC | | | intron-variant | USP36 | GRCh38.p7 | 17:78813273 | CAGAAAGCAAGAACC[-/CC]TCAAACACCTCAGCC | 57602 |
rs3088040 | snp | A/G | 0.495057 | 0.0500417 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803778 | CCAGTGAGCCCCCCC[A/G]GAGCCCCTCTGAGAA | 57602 |
rs3744791 | snp | G/T | 0.0433397 | 0.140682 | intron-variant | USP36 | GRCh38.p7 | 17:78827178 | GGTGGCAGCAGAACA[G/T]TCCTATGGCAACAGC | 57602 |
rs3744792 | snp | A/C | 0.0179029 | 0.0929027 | intron-variant | USP36 | GRCh38.p7 | 17:78827145 | GCCCGGCACCTTTCT[A/C]CCCAGGCTGCCCTTG | 57602 |
rs3744793 | snp | A/G | 0.489343 | 0.0722135 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821008 | GACCCCTACTTGGAC[A/G]TCGCGCTGGAGATCC | 57602 |
rs3744794 | snp | A/G | 0.000197772 | 0.00994217 | intron-variant | USP36 | GRCh38.p7 | 17:78818656 | CCAAGGTGAGCGCTC[A/G]TGACACCATCCCAGG | 57602 |
rs3744795 | snp | A/G | 0.0758518 | 0.179367 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807577 | GATTGGTGTGCCCAT[A/G]TCCAGGAATGGCTCC | 57602 |
rs3744796 | snp | A/G | 0.0119854 | 0.0764792 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807115 | CGATTCTCAGGAAAC[A/G]AACTGTTCCACCGCT | 57602 |
rs3744797 | snp | G/T | 0.0221062 | 0.102783 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803753 | TGAGAAGAGGAAAAA[G/T]ACCTTTGTGGGAGAG | 57602 |
rs3744799 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | USP36 | GRCh38.p7 | 17:78798692 | TGCAGGTCGCCGTGC[A/G]CAGGGGTCATTGTGA | 57602 |
rs3744800 | snp | C/T | 0.497473 | 0.0354532 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797743 | ACAGACCGCCCAACA[C/T]AGAGGCTTTGAGGCT | 57602 |
rs3744801 | snp | C/T | 0.499995 | 0.00159744 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797646 | GTGAGCAGAGGTGGC[C/T]GCACACCTGCTGGAC | 57602 |
rs3744802 | snp | C/T | 0.446641 | 0.154377 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797518 | GGTGGCCACATGTCC[C/T]CCAGGTGGTCTCCCG | 57602 |
rs3744803 | snp | A/G/T | 0.0490535 | 0.14873 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797451 | CTTCTCGGGGCTGAC[A/G/T]CCACCGTTGTGTCCG | 57602 |
rs3809895 | snp | A/G | 0.0437281 | 0.141251 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842763 | TGCATTAACAGAATA[A/G]TTGTATTGTCACCCA | 57602 |
rs3826552 | snp | C/T | 0.446641 | 0.154377 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797803 | GTGTGGGCTCTGCTG[C/T]GCTGGGAGCCTGTCA | 57602 |
rs4352096 | snp | C/T | 0.496314 | 0.0427728 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837834 | AGTGAAAGTAAGGAC[C/T]TCCTCCAGCACCTCA | 57602 |
rs4602087 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816870 | aagtatatacTGATG[A/G]ACATGCAGAAcatca | 57602 |
rs4796800 | snp | A/G | 0.248188 | 0.249993 | intron-variant | USP36 | GRCh38.p7 | 17:78808465 | TATGTTGCCCCGGCT[A/G]GCCTTGAATTCCTGA | 57602 |
rs4796817 | snp | C/T | 0.463559 | 0.129972 | intron-variant | USP36 | GRCh38.p7 | 17:78806566 | GCTGCCCAAGCTTCC[C/T]GCTGCAGAGGTGCCG | 57602 |
rs4796819 | snp | A/G | 0.230603 | 0.249246 | intron-variant | USP36 | GRCh38.p7 | 17:78840332 | GAAGGTGCCCGCCCC[A/G]GGGCCGCACCCGCCC | 57602 |
rs4796820 | snp | A/G | 0.214239 | 0.247429 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840446 | CAGCGGGCCCCGGCG[A/G]CCCCCATCACCGGCC | 57602 |
rs6501249 | snp | A/G | 0.496348 | 0.0425753 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787560 | ATCTCCGTTAGGGGC[A/G]CTGTTCGTGTGCTGG | 57602 |
rs6501250 | snp | C/T | 0.497271 | 0.0368399 | intron-variant | USP36 | GRCh38.p7 | 17:78812644 | GCAGTGAGCCGAGAT[C/T]GGAGATCGCACCACT | 57602 |
rs6501252 | snp | C/T | 0.130694 | 0.219696 | intron-variant | USP36 | GRCh38.p7 | 17:78817300 | gcccttgtggttaca[C/T]gacacctgaGTCTAC | 57602 |
rs6501253 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825617 | ATTCCTCCCATCTCA[C/T]AGCCCCAAATCCAAA | 57602 |
rs7206939 | snp | A/G | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820420 | gtgagctatgattgc[A/G]ccactgcactcctgc | 57602 |
rs7207007 | snp | A/C | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78820601 | AAGGCAGACCACCCT[A/C]CCGCACCCTGTAGCT | 57602 |
rs7207012 | snp | C/G | 0.148326 | 0.228391 | intron-variant | USP36 | GRCh38.p7 | 17:78820607 | GACCACCCTCCCGCA[C/G]CCTGTAGCTGCAGCA | 57602 |
rs7207246 | snp | A/G | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820830 | GAAAAACTCTAGAAA[A/G]AAACAGGTAAAGACA | 57602 |
rs7208551 | snp | G/T | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78820811 | AATAAAAGGATACGC[G/T]TAGGAAAAACTCTAG | 57602 |
rs7208858 | snp | C/T | 0.139564 | 0.224285 | intron-variant | USP36 | GRCh38.p7 | 17:78810247 | cccccaacagcttac[C/T]gaataTTCTCTGTGC | 57602 |
rs7209141 | snp | A/G | 0.139225 | 0.224118 | intron-variant | USP36 | GRCh38.p7 | 17:78810973 | acaaaaattagccgg[A/G]agtgctggcgggcac | 57602 |
rs7210763 | snp | C/T | 0.0157215 | 0.0872558 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814538 | TATGTTGAGGAATTC[C/T]GGATAGCCTACATCC | 57602 |
rs7210788 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | USP36 | GRCh38.p7 | 17:78825194 | GTCTCAGCAGCCACC[A/G]CCAAGCATGCAGGAA | 57602 |
rs7211645 | snp | C/T | 0.34303 | 0.232046 | intron-variant | USP36 | GRCh38.p7 | 17:78807874 | ACACCTGGCTAATTT[C/T]TGTATTTTTGACAGA | 57602 |
rs7211960 | snp | C/T | 0.386694 | 0.20932 | intron-variant | USP36 | GRCh38.p7 | 17:78808026 | ATATCTTTATGGCCA[C/T]CTTTACTATAAAACC | 57602 |
rs7212126 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | USP36 | GRCh38.p7 | 17:78808132 | ATAACCATGCATTAA[C/T]ATTCTAGTGCTTTCT | 57602 |
rs7212290 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | USP36 | GRCh38.p7 | 17:78826716 | GGCAACCATCACATA[C/T]AAGGGCTTACGTGGC | 57602 |
rs7213204 | snp | C/T | 0.496649 | 0.0407971 | intron-variant | USP36 | GRCh38.p7 | 17:78835718 | GCTTGGCTAAAGAAT[C/T]CAAGGGCCCCTCTAT | 57602 |
rs7215525 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | USP36 | GRCh38.p7 | 17:78840116 | GGCCGCGGACACAGC[A/G]ACCCGAGCACCTCTC | 57602 |
rs7216266 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78827571 | AGGCTTGAGCATTCA[C/T]TACTGCACAGACAAG | 57602 |
rs7216559 | snp | G/T | 0.189576 | 0.242588 | intron-variant | USP36 | GRCh38.p7 | 17:78827576 | TGAGCATTCACTACT[G/T]CACAGACAAGGAAGA | 57602 |
rs7216626 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78827802 | tagtcccagctactt[A/G]ggtggctgaggcagg | 57602 |
rs7217047 | snp | A/G | 0.131723 | 0.220251 | intron-variant | USP36 | GRCh38.p7 | 17:78827844 | agcctaggaggttga[A/G]gctgcagtgagctat | 57602 |
rs7217654 | snp | A/G | 0.304188 | 0.244057 | intron-variant | USP36 | GRCh38.p7 | 17:78815225 | TAGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57602 |
rs7217867 | snp | C/T | 0.141258 | 0.225111 | intron-variant | USP36 | GRCh38.p7 | 17:78822527 | CGGCTCTGCACCCGT[C/T]TCAGAGAGGACAGCG | 57602 |
rs7218057 | snp | C/T | 0.169435 | 0.236663 | intron-variant | USP36 | GRCh38.p7 | 17:78822670 | CCCGGGGCTGCCTGG[C/T]GCCTCCCACGCCTAC | 57602 |
rs7218605 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | USP36 | GRCh38.p7 | 17:78815721 | ATAGAAAAAAataca[C/T]gcacacatatacata | 57602 |
rs7219360 | snp | C/T | 0.134119 | 0.221521 | intron-variant | USP36 | GRCh38.p7 | 17:78822702 | TATCCATATGGTAGC[C/T]ACTCACGCTGGAAGG | 57602 |
rs7220532 | snp | C/T | 0.497211 | 0.037236 | intron-variant | USP36 | GRCh38.p7 | 17:78812691 | GACAGAGCGAGACTC[C/T]GTCTCGAAAAAAAAA | 57602 |
rs7222131 | snp | A/G | 0.337841 | 0.23406 | intron-variant | USP36 | GRCh38.p7 | 17:78820117 | AGGCAGCAAATCACA[A/G]AACTTAGACTCGCAT | 57602 |
rs7223832 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78804664 | AAAAAGCAAGCCAAC[A/C]CGTGATTTTAAAAGT | 57602 |
rs7224190 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832438 | CAAGATAGTAAGATG[C/T]ACTAATATTTCACAG | 57602 |
rs7224341 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832601 | cggggatttacagat[A/G]ttatctagttttaac | 57602 |
rs7224531 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832760 | TGAGACGAAAACAAC[A/G]GCCATCTAGTCAAAT | 57602 |
rs7224590 | snp | A/G | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78832540 | cttactcacacgctt[A/G]ctgctgacatgctgc | 57602 |
rs7225821 | snp | A/G | 0.213937 | 0.247385 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841775 | TGTGTCTTTTTTGAT[A/G]TAAGTAGGAATGATG | 57602 |
rs7226033 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | USP36 | GRCh38.p7 | 17:78792706 | TCACTATGATCCCCC[C/T]GGGAAGGtttttttt | 57602 |
rs7226043 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825683 | GAATTTCTTCCACCG[C/T]AGACTCTGGTTAATT | 57602 |
rs7226193 | snp | A/G | 0.335788 | 0.23482 | intron-variant | USP36 | GRCh38.p7 | 17:78820596 | CAGCAAAGGCAGACC[A/G]CCCTCCCGCACCCTG | 57602 |
rs7226316 | snp | A/G | 0.169435 | 0.236663 | intron-variant | USP36 | GRCh38.p7 | 17:78792758 | gagtctcactctgtc[A/G]cccaggctggagtgc | 57602 |
rs8064351 | snp | C/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78825941 | ATTGGCCACACCACA[C/T]TGCAAACGCTGCTGG | 57602 |
rs8065170 | snp | A/G | 0.0191375 | 0.0959297 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821009 | GATCTCCAGCGCGAC[A/G]TCCAAGTAGGGGTCG | 57602 |
rs8068534 | snp | A/T | 0.131381 | 0.220067 | intron-variant | USP36 | GRCh38.p7 | 17:78826267 | aggaatggtggctca[A/T]gcctgtaatcccagc | 57602 |
rs8069001 | snp | C/T | 0.134802 | 0.221877 | intron-variant | USP36 | GRCh38.p7 | 17:78821279 | TTGCACTCACAGGGC[C/T]CTCCCTGCCTGGACT | 57602 |
rs8069028 | snp | A/C | 0.135143 | 0.222054 | intron-variant | USP36 | GRCh38.p7 | 17:78821381 | TGCACGGCACTTCCT[A/C]ATGAGAatatatata | 57602 |
rs8069157 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821420 | tatatatatatatat[A/T]ttttttttttttttt | 57602 |
rs8069830 | snp | C/T | 0.186737 | 0.241863 | intron-variant | USP36 | GRCh38.p7 | 17:78821776 | GCTCCAGTGGCCAGG[C/T]GGGCCAAGAGTCTCA | 57602 |
rs8071100 | snp | G/T | 0.33875 | 0.233717 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786996 | tttattttttgagac[G/T]gagtctcgctctgtt | 57602 |
rs8072569 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | USP36 | GRCh38.p7 | 17:78790918 | TGGCAGCCATGTCCT[A/G]TTGCTTCCTCTAATC | 57602 |