SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3612 | snp | A/C | 0.425894 | 0.177655 | utr-variant-3-prime | USP22 | GRCh38.p7 | 17:21001771 | CCTTGTCCCTAGTTT[A/C]TAATTTCTCAGTGGA | 23326 |
rs6618 | snp | G/T | 0.482534 | 0.0918038 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:20999755 | TTTGAAAATAAAAAT[G/T]AAGAAAAAAATTCCA | 23326 |
rs716959 | snp | C/T | 0.263809 | 0.249618 | intron-variant | USP22 | GRCh38.p7 | 17:21013277 | CACCATATGTTCAGC[C/T]GTCTCACTGGAACAA | 23326 |
rs719093 | snp | C/T | 0.314544 | 0.241524 | intron-variant | USP22 | GRCh38.p7 | 17:21013049 | GTGTCCTCACATGGC[C/T]TTTTAAAGCGTTGGC | 23326 |
rs719094 | snp | A/C | 0.393619 | 0.204631 | intron-variant | USP22 | GRCh38.p7 | 17:21013484 | CACACATGGATATGA[A/C]TGAAGTGTGTATTGA | 23326 |
rs899340 | snp | C/T | 0.485528 | 0.0838238 | intron-variant | USP22 | GRCh38.p7 | 17:21009535 | TCTCTCCTAACAACA[C/T]AGGCTTCCCACACAT | 23326 |
rs899341 | snp | G/T | 0.435694 | 0.167385 | intron-variant | USP22 | GRCh38.p7 | 17:21020957 | ATGCAGAGCTTCAGC[G/T]GACTCCACTGTGGGC | 23326 |
rs899342 | snp | C/T | 0.395635 | 0.2032 | intron-variant | USP22 | GRCh38.p7 | 17:21021307 | CAGAGTTAAACACAG[C/T]GAGGTTCTGTAGATA | 23326 |
rs984007 | snp | A/G | 0.414576 | 0.188188 | intron-variant | USP22 | GRCh38.p7 | 17:21018955 | AGAGCTGGTTGCTGA[A/G]CACATTGATGAGTGA | 23326 |
rs996065 | snp | C/T | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21033090 | GGCTGACATGGACCG[C/T]GGAGGGGTGGCACTG | 23326 |
rs1038107 | snp | C/T | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21018179 | GTCGCTGGATCCCAG[C/T]GGCTTCCTCTACCTC | 23326 |
rs1038108 | snp | A/C | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21018235 | TCATTCAAGCCAGAA[A/C]ACGATGAGATATCGC | 23326 |
rs1038109 | snp | A/G | 0.426047 | 0.177503 | intron-variant | USP22 | GRCh38.p7 | 17:21019978 | AGATTGCTCTCCAGA[A/G]AAGACTTGTTAAACA | 23326 |
rs1044410 | snp | C/T | 0.424193 | 0.179323 | utr-variant-3-prime, downstream-variant-500B | USP22, LOC105369205 | GRCh38.p7 | 17:21001356 | GGGCTGGGGAGGGGG[C/T]AGTGACAGTGGCAGC | 23326 |
rs1044414 | snp | C/T | 0.424348 | 0.179172 | utr-variant-3-prime, downstream-variant-500B | USP22, LOC105369205 | GRCh38.p7 | 17:21001138 | AGATGGGCCGAGATT[C/T]TCAGAAATGGTCCCA | 23326 |
rs1044420 | snp | A/G | 0.492237 | 0.0618148 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:21000463 | GGTGGGCATTATTCT[A/G]AACTTTCGTATCCAA | 23326 |
rs1045162 | snp | G/T | 0.316485 | 0.240998 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:20999767 | GTTTACTGTAAGTTT[G/T]AAAATAAAAATGAAG | 23326 |
rs1045215 | snp | C/G | 0.263535 | 0.249633 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:20999646 | CACTCCTCCTCCCCC[C/G]CAGTGCTTTGTAGTC | 23326 |
rs1061971 | snp | C/T | 0 | 0 | utr-variant-3-prime | USP22 | GRCh38.p7 | 17:21001966 | GGAGCCTGCATCTTG[C/T]CTCGTCTGCCTCTGC | 23326 |
rs1115509 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | USP22 | GRCh38.p7 | 17:21025641 | aatgtggtctacata[A/C]acaatggaacatgac | 23326 |
rs1127814 | snp | C/T | 0.316 | 0.241131 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:21000979 | CACTGCAACCTCCAC[C/T]TCCTGGGTTCAAGCA | 23326 |
rs1127815 | snp | A/G | 0.424193 | 0.179323 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:21000918 | GGACTACAGGCATGC[A/G]CCACCACGCCAGGCT | 23326 |
rs1382513 | snp | A/G | 0 | 0 | intron-variant | USP22 | GRCh38.p7 | 17:21030384 | TGTGTGTGTGTGTGT[A/G]TGTATGTATGTATGT | 23326 |
rs1478790 | snp | A/G | 0.0821764 | 0.185298 | upstream-variant-2KB | USP22 | GRCh38.p7 | 17:21045385 | CTAACTAGTAAGTCA[A/G]GAATTACAAAAATAT | 23326 |
rs1904230 | snp | C/G | 0.426966 | 0.176587 | intron-variant | USP22 | GRCh38.p7 | 17:21040907 | ACAGAGCAAGACCCC[C/G]TCCGGAAAAAAAAAA | 23326 |
rs1993901 | snp | A/G | 0.426966 | 0.176587 | intron-variant | USP22 | GRCh38.p7 | 17:21035478 | TACAGGAAAAGCCTT[A/G]ATAGGAGACCCTGct | 23326 |
rs2054463 | snp | C/G | 0.426354 | 0.177198 | intron-variant | USP22 | GRCh38.p7 | 17:21016392 | AGCTCAACTCCAGCC[C/G]CAGACCCAGCAGCAC | 23326 |
rs2054464 | snp | C/T | 0.314787 | 0.241459 | intron-variant | USP22 | GRCh38.p7 | 17:21016407 | GCAGACCCAGCAGCA[C/T]ACCTTCCATCCCACG | 23326 |
rs2127093 | snp | A/C | 0.428484 | 0.175052 | intron-variant | USP22 | GRCh38.p7 | 17:21016390 | ACAGCTCAACTCCAG[A/C]CGCAGACCCAGCAGC | 23326 |
rs2127094 | snp | A/G | 0.421684 | 0.181726 | intron-variant | USP22 | GRCh38.p7 | 17:21022006 | TCGGGGAGCTGAGGC[A/G]TGAGAACAGCTGAAA | 23326 |
rs2127095 | snp | A/G | 0.322959 | 0.239117 | intron-variant | USP22 | GRCh38.p7 | 17:21022070 | TTGCCACTGCACTCC[A/G]GCCTGGGCAACAGAG | 23326 |
rs2127096 | snp | C/T | 0.414576 | 0.188188 | intron-variant | USP22 | GRCh38.p7 | 17:21030814 | ggattgaatcctata[C/T]gccaatttttaaagg | 23326 |
rs2291034 | snp | G/T | 0.286798 | 0.247277 | intron-variant | USP22 | GRCh38.p7 | 17:21007860 | AGAGTTGGCTTTCTG[G/T]AAAACTTACTTTGAG | 23326 |
rs2291035 | snp | A/G | 0.374202 | 0.216965 | intron-variant | USP22 | GRCh38.p7 | 17:21011322 | CCACTGGAAGCAGAG[A/G]GAAAACAATGGCTGT | 23326 |
rs2291036 | snp | C/G | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21019389 | CACAGAGGGTATGAG[C/G]ATGTGAGCTACGTTT | 23326 |
rs2291037 | snp | A/G | 0.393376 | 0.204801 | synonymous-codon | USP22 | GRCh38.p7 | 17:21021210 | ACAGTAGATGCCTCC[A/G]TACATCAGATCAATG | 23326 |
rs2291038 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP22 | GRCh38.p7 | 17:21028846 | CTTTCAGTTCCCCCA[A/C/G]ACAGGACTTCATTCA | 23326 |
rs2364326 | snp | C/T | 0.322959 | 0.239117 | intron-variant | USP22 | GRCh38.p7 | 17:21036151 | ctttccagaatgtca[C/T]atcattgggttcata | 23326 |
rs2364327 | snp | C/G | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21036111 | gccttttcatactgg[C/G]ttcttttgtctagca | 23326 |
rs2364328 | snp | A/G | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21036096 | cttcttttgtctagc[A/G]atatccattgtatcc | 23326 |
rs2364329 | snp | C/G | 0.426201 | 0.177351 | intron-variant | USP22 | GRCh38.p7 | 17:21019612 | CTTAGTTTGGTAACT[C/G]GACGCTGAGTTTATG | 23326 |
rs2364330 | snp | C/G | 0.426201 | 0.177351 | intron-variant | USP22 | GRCh38.p7 | 17:21019607 | TTTGGTAACTCGACG[C/G]TGAGTTTATGCTATT | 23326 |
rs2364331 | snp | A/T | 0.426354 | 0.177198 | intron-variant | USP22 | GRCh38.p7 | 17:21019604 | GGTAACTCGACGCTG[A/T]GTTTATGCTATTTCA | 23326 |
rs2364332 | snp | C/T | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21005975 | CCCTGGCTTCCGGGT[C/T]ACATGGCCAGCTCCC | 23326 |
rs2364333 | snp | C/T | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21005897 | ATTGGCTTTAGGACC[C/T]AGGCAGATCATCCAG | 23326 |
rs2886049 | snp | C/T | 0.312837 | 0.241974 | intron-variant | USP22 | GRCh38.p7 | 17:21009942 | AGACGGAGTCTCGCT[C/T]TTTCTAGAGTGCAGG | 23326 |
rs3047597 | in-del | -/TTTTTT | | | intron-variant | USP22 | GRCh38.p7 | 17:21020245 | ttttttttttttttt[-/TTTTTT]GGTTTTTGATTCTGA | 23326 |
rs3047599 | in-del | -/TT | 0.42666 | 0.176893 | intron-variant | USP22 | GRCh38.p7 | 17:21019668 | TTACCACCACTCTCT[-/TT]GAATATTTTGTGGCA | 23326 |
rs3047630 | in-del | -/CTT | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21018225 | ATCGTGTTCTGGCTT[-/CTT]GAATGAATGAATAAA | 23326 |
rs3047631 | in-del | -/TTA/TTTA | 0.260504 | 0.249779 | intron-variant | USP22 | GRCh38.p7 | 17:21009972 | GATTTTTTTTTTTTT[-/TTA/TTTA]AATTTTTTTTTTTTG | 23326 |
rs3203817 | snp | C/G | 0 | 0 | utr-variant-3-prime | USP22, LOC105369205 | GRCh38.p7 | 17:21000155 | TCTGACCACTAAGGG[C/G]CCCCCTTGGTGACCC | 23326 |
rs3214918 | in-del | -/T | 0.260865 | 0.249764 | utr-variant-3-prime | USP22 | GRCh38.p7 | 17:21002959 | CTTGGGGGAGGGGGG[-/T]GGCCAGGGAGGATCA | 23326 |
rs3785544 | snp | C/T | 0.258565 | 0.249853 | intron-variant | USP22 | GRCh38.p7 | 17:21012202 | CTAAGGAGGGAGGAT[C/T]GCTTGAGCCCATGGG | 23326 |
rs3816664 | snp | C/T | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21015521 | GTCACTGAGGACCTG[C/T]CATACTGCTGGAACT | 23326 |
rs3943299 | snp | A/C | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21017298 | GCTCCTGTGCAAGGC[A/C]CCTGAAGAACAGGCA | 23326 |
rs4133914 | snp | A/G | 0.424348 | 0.179172 | intron-variant | USP22 | GRCh38.p7 | 17:21018710 | CTCAAAAAAGAAAAA[A/G]AAAAAGTTTTAAAGG | 23326 |
rs4270230 | snp | G/T | 0.5 | 0 | intron-variant | USP22 | GRCh38.p7 | 17:21031590 | GTTGTGTAGTAGAGA[G/T]AGACTATAATGGAGT | 23326 |
rs4445951 | snp | C/G | 0.314544 | 0.241524 | intron-variant | USP22 | GRCh38.p7 | 17:21009911 | CTGGAGTGCAGTGGC[C/G]CGATCTTGGCTCACT | 23326 |
rs4613123 | snp | C/T | 0.421684 | 0.181726 | intron-variant | USP22 | GRCh38.p7 | 17:21025982 | atgagccaccgcgcc[C/T]ggccCTattaaccat | 23326 |
rs4985820 | snp | G/T | 0.425894 | 0.177655 | intron-variant | USP22 | GRCh38.p7 | 17:21028347 | AGAACCATCGGATGC[G/T]AAGGCAAACTGAGGA | 23326 |
rs4985822 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | USP22 | GRCh38.p7 | 17:21033818 | CAGTGGCGTAATCTC[C/G]GCTAACTGCAACCTC | 23326 |
rs4985823 | snp | A/C/G/T | | | intron-variant | USP22 | GRCh38.p7 | 17:21042428 | ttcccctctcccccc[A/C/G/T]tcccccattcttcct | 23326 |
rs4985956 | snp | C/T | 0.499784 | 0.0103811 | utr-variant-3-prime | USP22 | GRCh38.p7 | 17:21002938 | AGGCCGGGGAGGCGG[C/T]GGGAGACTTGGGGGA | 23326 |
rs4985957 | snp | A/G | 0.427727 | 0.175821 | utr-variant-3-prime | USP22 | GRCh38.p7 | 17:21002944 | GGGAGGCGGCGGGAG[A/G]CTTGGGGGAGGGGGG | 23326 |
rs4985958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP22 | GRCh38.p7 | 17:21003969 | AAACAACTGCTCTGA[C/T]GTTCTCTGTGCTAAG | 23326 |
rs4985959 | snp | A/G | 0.472896 | 0.113214 | intron-variant | USP22 | GRCh38.p7 | 17:21007521 | AGCTTGCCAACTCCT[A/G]GACCAGATCTGCATG | 23326 |
rs4985962 | snp | A/G | 0.424193 | 0.179323 | intron-variant | USP22 | GRCh38.p7 | 17:21012722 | TTAATCATTTATCTC[A/G]TAGCCTCCTTAAAGA | 23326 |
rs4985963 | snp | A/G | 0.498459 | 0.0277128 | intron-variant | USP22 | GRCh38.p7 | 17:21023746 | AAGACCATGGATTGA[A/G]AGTAACTGGCACCAG | 23326 |
rs4985964 | snp | G/T | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21023964 | TTTTATTCTATTTCA[G/T]GTCTTAAGCTACTAC | 23326 |
rs4985965 | snp | A/G | | | intron-variant | USP22 | GRCh38.p7 | 17:21031729 | TACACACTCCATTAT[A/G]GTCTATCTCTACTAC | 23326 |
rs4985966 | snp | C/T | 0.322959 | 0.239117 | intron-variant | USP22 | GRCh38.p7 | 17:21039020 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 23326 |
rs4985967 | snp | A/G | 0.497502 | 0.035255 | intron-variant | USP22 | GRCh38.p7 | 17:21042574 | AGGCAACGGGGGAAG[A/G]GAAGAGGGCAGGAAA | 23326 |
rs4992796 | snp | G/T | | | intron-variant | USP22 | GRCh38.p7 | 17:21009466 | GTAGAGTGCACCCGG[G/T]TCCCCACTTTGTATT | 23326 |
rs5005801 | snp | C/T | 0.426966 | 0.176587 | intron-variant | USP22 | GRCh38.p7 | 17:21040841 | GGAATGTGCTGTTGC[C/T]ACTCTGGGTCAGTAG | 23326 |
rs5819720 | in-del | -/CC | 0.426201 | 0.177351 | intron-variant | USP22 | GRCh38.p7 | 17:21009466 | AATACAAAGTGGGGA[-/CC]CGGGTGCACTCTACC | 23326 |
rs5819721 | in-del | -/T | 0.5 | 0 | intron-variant | USP22 | GRCh38.p7 | 17:21018441 | TGTTCTAGGGCCAGG[-/T]GCAGGGGCTCATACT | 23326 |
rs5819722 | in-del | -/A | | | intron-variant | USP22 | GRCh38.p7 | 17:21018715 | AAAGAAAAAGAAAAA[-/A]GTTTTAAAGGGTATT | 23326 |
rs5819724 | in-del | -/A | 0 | 0 | intron-variant | USP22 | GRCh38.p7 | 17:21035516 | AGGACAAAAAAAAAA[-/A]CAAACCACAACACTT | 23326 |
rs6587108 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP22 | GRCh38.p7 | 17:21013869 | CACGAGGTTAGGAGA[C/T]CGAGACCATCCTGGC | 23326 |
rs6587109 | snp | C/T | 0.405255 | 0.195948 | intron-variant | USP22 | GRCh38.p7 | 17:21014505 | ATTAAAAGGATCACG[C/T]AGTTTTTCAGAGGAA | 23326 |
rs6587111 | snp | A/T | 0.496583 | 0.0411924 | intron-variant | USP22 | GRCh38.p7 | 17:21026042 | aggcaggcgatcacc[A/T]gaggtcaggagttca | 23326 |
rs7207724 | snp | A/G | 0.424814 | 0.178718 | intron-variant | USP22 | GRCh38.p7 | 17:21020923 | TATGCATGCCTCGAC[A/G]CTAGCCACCTCCCCT | 23326 |
rs7207753 | snp | C/G | 0.434831 | 0.168337 | intron-variant | USP22 | GRCh38.p7 | 17:21016024 | TTGACACAAATGTTT[C/G]GATTTTACTTTTCTA | 23326 |
rs7208779 | snp | A/G | 0.421684 | 0.181726 | intron-variant | USP22 | GRCh38.p7 | 17:21037034 | gtgctcaaaaacaac[A/G]aacaaaaaataatgt | 23326 |
rs7209129 | snp | C/T | 0.49907 | 0.0215454 | intron-variant | USP22 | GRCh38.p7 | 17:21016191 | CAAATAAAAGTGACT[C/T]GATTTGCCCAATACT | 23326 |
rs7211094 | snp | C/T | 0.426201 | 0.177351 | intron-variant | USP22 | GRCh38.p7 | 17:21020437 | GGGCAGCTCACAAGA[C/T]GGCAAGGATCTGACT | 23326 |
rs7211862 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | USP22 | GRCh38.p7 | 17:21034304 | AGGCTGGGACCCAGC[A/G]GTTGCCGGTGATGTC | 23326 |
rs7212424 | snp | A/C/G | 0.0383715 | 0.133092 | intron-variant | USP22 | GRCh38.p7 | 17:21030931 | tgataactgtattgc[A/C/G]cttatgtaggagact | 23326 |
rs7213684 | snp | G/T | 0.434831 | 0.168337 | intron-variant | USP22 | GRCh38.p7 | 17:21016021 | CATTTGACACAAATG[G/T]TTGGATTTTACTTTT | 23326 |
rs7215369 | snp | A/G | 0.418974 | 0.184249 | intron-variant | USP22 | GRCh38.p7 | 17:21013543 | CAGAACTTAATTCGT[A/G]TGTGGAATACATATT | 23326 |
rs7215921 | snp | C/T | | | intron-variant | USP22 | GRCh38.p7 | 17:21038352 | CATCCCAGCACCTGG[C/T]TGAGCCAGTAAAGAC | 23326 |
rs7216030 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | USP22 | GRCh38.p7 | 17:21027690 | AAACAAAGCCAAggc[C/T]gggcacaatggttca | 23326 |
rs7216449 | snp | A/C | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21027563 | TTCCCTAAAACAGGT[A/C]TCTAGCTTGGACCGC | 23326 |
rs7216786 | snp | A/G | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21027751 | AGGCAGGAGGATCAC[A/G]TGAGGTCAGGAGTTT | 23326 |
rs7216803 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP22 | GRCh38.p7 | 17:21035379 | ATCCATTAGGCGGGT[C/T]ATTTTAATCCTTGAA | 23326 |
rs7216921 | snp | A/C | 0.48155 | 0.0942576 | intron-variant | USP22 | GRCh38.p7 | 17:21006528 | TTTTTTTTTTTTAGA[A/C]GTAGTCTCGTTCTGT | 23326 |
rs7216978 | snp | A/G | 0.43309 | 0.17023 | intron-variant | USP22 | GRCh38.p7 | 17:21022981 | tacatatataccatg[A/G]gataccatgtataca | 23326 |
rs7218443 | snp | C/G | 0.426813 | 0.17674 | intron-variant | USP22 | GRCh38.p7 | 17:21023125 | aagtgggagctaaac[C/G]attagaacacatgga | 23326 |
rs7219244 | snp | A/C | 0.421526 | 0.181876 | intron-variant | USP22 | GRCh38.p7 | 17:21023282 | actgtacaccaaacc[A/C]ctgaataatacgttt | 23326 |
rs7219504 | snp | C/G | 0.312348 | 0.242101 | intron-variant | USP22 | GRCh38.p7 | 17:21010564 | CACCTGTAGTCCCAG[C/G]TACTCAGGAGAATCA | 23326 |