SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs185549122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78803007 | GCAGTGACGCGATCT[C/T]AGCTCACTGCAACCT | 57602 |
rs185687034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799376 | AGGTTGGAAGAGCTT[C/T]GTCACTCTGCCCCTT | 57602 |
rs185789839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824109 | GCCACACACAGCTGC[C/T]CTCCTGGAGGAACTT | 57602 |
rs185872387 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP36 | GRCh38.p7 | 17:78812206 | AAAAAAAGTTTGCTT[G/T]GCATTATAAAGGAAA | 57602 |
rs185995304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78791934 | TCTACAGTAGAGATC[C/T]TGACAGAGGGTGGAT | 57602 |
rs186001931 | snp | A/G/T | 9.92431e-05 | 0.00704363 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807158 | GCTCCACTCCTGGGG[A/G/T]TCTGGGGGGCCTTGG | 57602 |
rs186006803 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78823380 | CCAGAAGCCCGCAAG[A/C]ACCAGCGCCCGCAGG | 57602 |
rs186091049 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796975 | TGAGTTATACAATCA[C/T]TTAAATTCCAAAGCA | 57602 |
rs186109101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788915 | TTCACGAAAGAGAGA[A/T]GAGGCCAGGTGCGGT | 57602 |
rs186109542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815876 | ACACATGTACGCATA[C/T]ACATACATGCACAAC | 57602 |
rs186125504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824799 | ACAGATCTTAAGAAC[A/G]CCTCTAAGAAAGGGT | 57602 |
rs186242377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78808698 | TATCCTTTACCCTTC[A/G]GAGCACTTATTACAA | 57602 |
rs186251976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820158 | CCACTAGCTGCCAGA[C/T]TGGGACTCCTTCTCC | 57602 |
rs186258834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829587 | GTCTAGTCACAACTA[C/T]GCTCCTGTATTGTAG | 57602 |
rs186345454 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792351 | GGCCTCAAGGGCACA[A/G]GTGGGGTGCCAGCAT | 57602 |
rs186358049 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | USP36 | GRCh38.p7 | 17:78812638 | GAGCTTGCAGTGAGC[C/G]GAGATTGGAGATCGC | 57602 |
rs186364949 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835108 | TGACCGATTCACCTT[C/T]ATGGCCCATTCTGCA | 57602 |
rs186444868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808224 | AAGCTATTATCTCAA[A/G]CATTTTTATGGGCGA | 57602 |
rs186621703 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78787715 | AGAACCTTTCCATAC[G/T]GTTATGGGTTGAGTC | 57602 |
rs186672577 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78816300 | AAGTAGCTGGGACTA[C/T]AGGCACGCGCCACCA | 57602 |
rs186744854 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78793005 | ACAGGTGTGAGCCAC[C/T]GCGCCCGCCCCCCTC | 57602 |
rs186886852 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797693 | CTCTTGCAGGGCTGG[C/T]CGGGAATGTCACCAA | 57602 |
rs186902784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834094 | TCTACTAAAAATACA[A/G]AAATTAGCCAGGCGT | 57602 |
rs186965868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799226 | CCCCAGCGATGCCCT[C/T]TTAGCTAAACCCTAA | 57602 |
rs187134289 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78838936 | ACCAGTTGTTGTAAT[A/G]CACACGATATGAACA | 57602 |
rs187253459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798361 | TACACGGCACACACA[C/T]CCCCACCTCACCCTT | 57602 |
rs187277584 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78802663 | GCACGCAGGTCCCTG[C/G]AACATTCTTCCCCCC | 57602 |
rs187299500 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838387 | AAAAAAAAAAAAAAA[A/C]AAAAAACAAAAAACT | 57602 |
rs187305159 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789582 | TCACACAGGCTTGGA[C/T]TGGGGCATTGTCTTG | 57602 |
rs187320894 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78825885 | GGGTCACTTCTCCCA[G/T]GAAGCCGCCTCTGGG | 57602 |
rs187464597 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841633 | ACTTCGCTGGCTTCC[A/T]CCCCATTCCCTTGGG | 57602 |
rs187478910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814095 | CCTAGTGCCCCAACA[G/T]ATAGGAACTGTCCCT | 57602 |
rs187502986 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78819875 | ACACTGTCAGGTGAG[A/G]GGACTTATTTCCCGT | 57602 |
rs187534909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805266 | TAAGTGTCTTCTGGA[A/G]TCTTTTCCAAAAAAG | 57602 |
rs187537926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821589 | TGTGCCACCGCGCCT[C/G]GCTGATTTTTGTATT | 57602 |
rs187688071 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78827019 | TCCTACCAAGCCGCC[A/C]CGGACCAGCAGGACG | 57602 |
rs187912008 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794302 | GTCTAAAAAGCACAT[C/T]AGACCTTGGTAACCC | 57602 |
rs187931920 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78814886 | AACCCGCGAGGCAGA[C/G]GTTGCAGTGAGCCGA | 57602 |
rs187932197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831707 | GAACATTTTGGGAGG[C/G]TGACGCAGGAGGATC | 57602 |
rs188004316 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP36 | GRCh38.p7 | 17:78809754 | TCAACCTCCAAACAG[C/T]TGGGACAACAGACGT | 57602 |
rs188029456 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796324 | GAACATACCCTGCCC[A/G]TGAAGGCATGTGCTT | 57602 |
rs188033465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822065 | ACACGAGGGATGGCC[C/G]CATCCCAGCAGCCCC | 57602 |
rs188035205 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842333 | CAGGGCACAGTGGCT[C/T]ACGCCTGTAATCCTA | 57602 |
rs188042684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815341 | ATCTCAAAACAATCA[A/G]AACAAACAAACAAAG | 57602 |
rs188058502 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78810336 | TCTGTTGCCCAGGCT[A/G]GTGTGGAGTGGTATG | 57602 |
rs188268607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78790465 | CCGGCTAATTTTTTT[G/T]TATTTTTAGTAGAGA | 57602 |
rs188269557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78819558 | CCTGGGGCGGCCGCC[C/T]GGTGCCAGCCAGTGT | 57602 |
rs188287117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838110 | TTAAAACAAAAAAAA[C/T]CGTGGCTCACGCCTG | 57602 |
rs188288464 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826126 | GGGAGCAAGGAAGCT[C/T]GAGCCCCTTCAGGAG | 57602 |
rs188478287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790980 | AAACCAATGAAAACA[C/T]GCATGCAAGACATGT | 57602 |
rs188523854 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78799599 | GCACCAGGATCCATT[C/G]CACACCCTTCCCTCC | 57602 |
rs188532641 | snp | C/T | 0.000350096 | 0.0132259 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836394 | GGACAAGAAGAAACA[C/T]AGAGCCATAGATAAC | 57602 |
rs188544356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792702 | CTGCTCACTATGATC[A/C]CCCCGGGAAGGTTTT | 57602 |
rs188552508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78830721 | CATGCAGCCTGCTTA[C/G]CAAATAGACATTAAA | 57602 |
rs188573663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801265 | ACAGGCGTGAGCCAC[A/C]ACCCCCGGCCAGGGC | 57602 |
rs188593464 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78819015 | AAGCAAAAAAATAAA[A/G]GTACTGTACCCACCA | 57602 |
rs188776643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78804582 | CAAACCTTTACATCC[C/T]GCACATGTACCCTGG | 57602 |
rs188804788 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841299 | GTGGAGAAGCGGAGG[C/T]GCGGGCGCTCGGCCT | 57602 |
rs188829377 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78813177 | AGTGAGGCTGAGAGA[C/T]CAGCCCCAAGTATCT | 57602 |
rs188950446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810993 | CTGGCGGGCACCTGT[A/G]ATTACAGCTACTCAG | 57602 |
rs188964758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828544 | TAAGAGGCTTCCCCA[A/C]TGACCCCAGCCCACA | 57602 |
rs189193200 | snp | C/T | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787120 | AGCTGGGATTACACG[C/T]ACGCGCTACCACGCC | 57602 |
rs189197588 | snp | A/G | 0.000204023 | 0.010098 | intron-variant | USP36 | GRCh38.p7 | 17:78807674 | CACAACTGAGGAAGC[A/G]AGAAGTCTCAGCTGG | 57602 |
rs189204015 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP36 | GRCh38.p7 | 17:78823462 | CACCTTCCCCAGGAG[A/G]AGGAAAGGCAAGCTG | 57602 |
rs189262783 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833080 | TTGAACACAGGAGGC[A/G]GGGGTTGCAGTGAGC | 57602 |
rs189292618 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78802225 | CAGTGCACGCCCATG[A/C]GGTCCCCCAACCCCT | 57602 |
rs189330884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805468 | ATTCTAGAACTAGAA[C/G]CCAGCGCCGAGGCCA | 57602 |
rs189529620 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78811758 | CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 57602 |
rs189666197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798653 | ACAGGCCGGGCTCTC[A/G]TGAGCTCTCTGGAGA | 57602 |
rs189676345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817530 | GAGGCTGAGGCAGGC[A/G]GATCACCTGAGCTCA | 57602 |
rs189691581 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78835168 | AGTTACTATACATTA[A/T]GAACTACCCTCCTAA | 57602 |
rs189794632 | snp | A/T | 0.000230962 | 0.0107437 | intron-variant | USP36 | GRCh38.p7 | 17:78820041 | AAACAGGGAGTAAAA[A/T]ACACAGCAGAGGAAA | 57602 |
rs189803882 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78791572 | GCTAAGAACAAGCAC[A/C]TTTTTAATCTCAGGC | 57602 |
rs189810277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78828831 | GCAACATAGCGAGAA[C/T]CCCATCTCTACAAAA | 57602 |
rs189848780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792143 | GATGATGGCAGAAGC[C/T]AGACTAAGAACCACA | 57602 |
rs189916827 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840429 | CCTGAATCCTGCACA[A/G]ACAGCGGGCCCCGGC | 57602 |
rs190052015 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78838499 | ATGAGAATTATCAAA[C/G]ACTTCTCACCAACTG | 57602 |
rs190096259 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795384 | GGAGATGCGGGGAGC[C/T]ACACACATCAGGTAA | 57602 |
rs190112361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832446 | TAAGATGCACTAATA[C/T]TTCACAGTGATACTG | 57602 |
rs190132127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802822 | CAGATCCTGGCCTGG[C/G]CCGGGACACCTGATC | 57602 |
rs190215172 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78803013 | ACGCGATCTCAGCTC[A/C]CTGCAACCTCCACCT | 57602 |
rs190229839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820241 | GCACCTTGGGAGGCC[A/G]GGGCAGGAGGATCAT | 57602 |
rs190235110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839038 | ATCTTATTTCCAAAG[A/G]GTAAGAGGTAATAAA | 57602 |
rs190306411 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78792419 | GGTCCCCACAGAGGA[C/T]GGGGAACAGCCCCTA | 57602 |
rs190331920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830237 | CAATAAATGGCACTG[A/T]AGCTACATGTTTCCA | 57602 |
rs190343069 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815061 | GATGCTGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 57602 |
rs190353324 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842630 | AAAGAAATGCAACGT[A/T]GGTCTCTCACGAAAT | 57602 |
rs190434027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806444 | GGGAGGTGAGGGGCA[A/G]GGGAATGGTAGAAGA | 57602 |
rs190578429 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78825948 | ACACCACATTGCAAA[C/T]GCTGCTGGGGTCCAC | 57602 |
rs190588138 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78822718 | ACTCACGCTGGAAGG[C/T]TCTGAAACAATACAC | 57602 |
rs190674239 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78788451 | TACAGGCGTGAGCCA[A/C]CGCACCCGGCCCTGG | 57602 |
rs190840278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78804098 | AAGGCTTTTACCCTG[C/T]AGTTTTCAGATACAC | 57602 |
rs190862140 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797170 | TATTGCAGCTGCAAG[A/G]GAAGCTACAGCACAG | 57602 |
rs190866153 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78815935 | ACACATACACACACA[A/T]ATACACACATGCATG | 57602 |
rs190873709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78788950 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCT | 57602 |
rs190922226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78829308 | ATGATCCTTTTCAGA[C/T]TTCACTAGTATTATT | 57602 |
rs191097332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820400 | GCCTAGAGGTCAACA[C/G]TACAGTGAGCTATGA | 57602 |
rs191176631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78813623 | TTTACTAAAAAGTGT[C/T]CTTCCCTGTGGACGG | 57602 |
rs191334267 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78830942 | CATTTAAAAGAAAAT[A/G]CAGGCCAGATGCAGT | 57602 |
rs191417270 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78792953 | ACTTCTGACCTCAAG[A/T]GATCCGCCCGCCTCA | 57602 |
rs191489802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793246 | AATTCTTGAGGTAGC[C/T]TTGGAAGTCACTTAC | 57602 |
rs191504140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78814195 | GCGGCTGCCTCTTCC[A/G]TGTCTCCCTGCAAGT | 57602 |
rs191509549 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831302 | TCCAAAACCTAACTT[C/T]AGGTAAGATACAGTT | 57602 |
rs191598285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805390 | TGTGTATATGTGAGA[C/G]GAGAGTAAGGCAGAG | 57602 |
rs191600495 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78821697 | CCTGCCTCGGCCTCC[A/C]AAAGTGCTGGGATTA | 57602 |
rs191614145 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841661 | GGGCAGGTTGAGAGT[A/G]TTGGTTCCTGGCCTG | 57602 |
rs191737837 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797813 | CCAGCGCAGCAGAGC[C/T]CACACAGAGAGCTCC | 57602 |
rs191842351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78801730 | CACTTTTGAACCCAA[A/C]TCTTCTAAATTCAAC | 57602 |
rs191857216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78819191 | ACAGAAGCAGAGGCG[C/T]GCAGCTTGGAGAGCT | 57602 |
rs191860114 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837208 | CTCCATTACACAGTG[C/T]TTGGAGTACAAATTA | 57602 |
rs191931947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78816790 | CCTAAATCATTTTTT[C/T]AAACTGAGTTGTGGG | 57602 |
rs191950213 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78808792 | CAAGAGGCTGTACCC[A/G]TTATCTCTCTCGTTC | 57602 |
rs192149278 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789844 | GAAAAACAAAGGGGG[C/T]GCGGGTAGGGCTCAG | 57602 |
rs192160831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78809587 | ATCTCCACCCTCGGG[C/T]ATCACTCTGCCCATG | 57602 |
rs192178000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78790485 | TTTAGTAGAGACAGG[G/T]TTTCACTATGTTAGC | 57602 |
rs192292211 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78825522 | CCACCTGACACCTGG[C/T]CTCCCTCCTCTTTCC | 57602 |
rs192328845 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842336 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 57602 |
rs192460975 | snp | C/T | 0.000109328 | 0.00739272 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835480 | ACTCCGTCACCACAG[C/T]TCTCATACGTGTGCT | 57602 |
rs192461394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790984 | CAATGAAAACACGCA[G/T]GCAAGACATGTATCG | 57602 |
rs192465633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810344 | CCAGGCTGGTGTGGA[A/G]TGGTATGATCATGAC | 57602 |
rs192569413 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | USP36 | GRCh38.p7 | 17:78810256 | GCTTACTGAATATTC[C/T]CTGTGCTGATGGGAT | 57602 |
rs192571785 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840851 | CACGTGTCACCGCGA[C/T]GCTTAAAGGCGCCGC | 57602 |
rs192654982 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814905 | GCAGTGAGCCGAGAT[C/T]GAGCCACTGCACTCA | 57602 |
rs192661691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831711 | ATTTTGGGAGGCTGA[C/T]GCAGGAGGATCGCTG | 57602 |
rs192715755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822300 | CCCCGAGAAATGTAC[A/G]TGTATCCTCACCCAG | 57602 |
rs192780933 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78826156 | GAAGGGGAAGAACGC[A/G]TGACCAAACCCTCAA | 57602 |
rs192823009 | snp | C/G | 6.93289e-05 | 0.00588724 | intron-variant | USP36 | GRCh38.p7 | 17:78821075 | CACTGCAACAGAACA[C/G]AGGCAGTGGAGCAGG | 57602 |
rs192825204 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78794709 | CGGGCAGATCACGAG[A/G]TCAAGAGATGGAGAT | 57602 |
rs192940993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800186 | TAGTGTTAAGTCCTC[A/G]GTCTGACAGAAGGAG | 57602 |
rs192951117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836553 | ACTAATCACTTGGAC[A/G]TATTAGTTCACATTT | 57602 |
rs193176907 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78818834 | TCGTGCTCTGAAAAA[C/T]GTTGTCTTAACGCTA | 57602 |
rs193230875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799243 | TAGCTAAACCCTAAA[A/C]CACAGCCAAAGAGTT | 57602 |
rs193291888 | snp | G/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841325 | GGCCTTAACGTCCCG[G/T]GCTCTGGGGCCATCC | 57602 |
rs199509578 | snp | C/T | 0.000708618 | 0.0188098 | intron-variant | USP36 | GRCh38.p7 | 17:78819918 | TTCTGCCACAAGCAA[C/T]GTGAAACTTACTTAG | 57602 |
rs199516494 | snp | A/G | 0.000100568 | 0.00709042 | intron-variant | USP36 | GRCh38.p7 | 17:78799803 | GAAACATTTACAGAC[A/G]TTTAAAATAACCCAC | 57602 |
rs199524982 | in-del | -/AC | | | intron-variant | USP36 | GRCh38.p7 | 17:78815839 | CACACATATATACAT[-/AC]ACACACACATATGCA | 57602 |
rs199596573 | snp | A/G | 8.25825e-05 | 0.0064253 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836071 | CCACTTCGTCACCCC[A/G]GAGTGAGGGCCTCTC | 57602 |
rs199617834 | snp | A/C/G | 3.3105e-05 | 0.00406837 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807487 | GTGTGTGGGTGTCTG[A/C/G]GAGAGTTTGGGGGAA | 57602 |
rs199718033 | snp | A/G/T | 9.26814e-05 | 0.00680686 | intron-variant | USP36 | GRCh38.p7 | 17:78827231 | CCTGGGAGGGTGGGT[A/G/T]GGGAAGCACGCACTT | 57602 |
rs199750041 | snp | A/C/G/T | 0.000148414 | 0.00861334 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806237 | TCGGAGGATGGTGAG[A/C/G/T]GGGGAGGTGGACGGA | 57602 |
rs199764785 | snp | C/T | 0.000458097 | 0.0151274 | intron-variant | USP36 | GRCh38.p7 | 17:78806930 | AGCTCTCCTGATACA[C/T]AGCAGCGGCGAGACC | 57602 |
rs199789383 | snp | A/G | 0.00317607 | 0.0397234 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802526 | ATCACCATCACCCAT[A/G]GGAGAGCAGCTGCTT | 57602 |
rs199792679 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811156 | AAAAAAAAAAAAAAA[C/T]AAACAGTCATCAAGA | 57602 |
rs199798175 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819154 | AGCAAAGCTAGAAGA[G/T]GCGCAAACACAGGGA | 57602 |
rs199829875 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835017 | TATATATATATATAT[A/T]TTTTGGAAGTATCTT | 57602 |
rs199832721 | snp | C/T | 0.000164734 | 0.00907413 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836149 | TCTCCACTCTTGTGG[C/T]GACTAGCTCCCTCTG | 57602 |
rs199843325 | snp | C/T | 6.58968e-05 | 0.00573969 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798427 | GGGCACAGTCAGCGG[C/T]GATAGCTGAGGCTGG | 57602 |
rs199852676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78788718 | TCCATGGGGTAGGTA[A/G]TGCTGAGGCCATCAG | 57602 |
rs199873425 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818749 | CTGTGGATGGTGAAG[C/T]GCTTGCTGGCTGGAA | 57602 |
rs199886203 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828939 | GCTTGATGGCGTTGC[C/T]GCTGTTGGCGAAGGC | 57602 |
rs199948498 | snp | C/G | 0.00016475 | 0.00907457 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798498 | AGTCTGAAGTTTCTG[C/G]AAGGCGTTGAAGTTT | 57602 |
rs199986026 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789035 | AAACTCCGTCTCTAT[A/T]AAAATATGAAAATTA | 57602 |
rs199991870 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | USP36 | GRCh38.p7 | 17:78819112 | ATGTGGCTGAGTGAT[-/A]AAACGGGCAGGCAGG | 57602 |
rs200013772 | snp | C/T | 0.00532698 | 0.0513334 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802466 | TGTCTCCTGCTTTCT[C/T]TTTTTCTTTTTCTTT | 57602 |
rs200027145 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | USP36 | GRCh38.p7 | 17:78810150 | GTAGACAAGGTCTCA[-/C]CTCTGTCACCTTGCC | 57602 |
rs200029537 | snp | C/T | 0.000338352 | 0.0130024 | intron-variant | USP36 | GRCh38.p7 | 17:78806936 | CCTGATACACAGCAG[C/T]GGCGAGACCCCCACA | 57602 |
rs200030393 | snp | A/G/T | 0.000131915 | 0.00812054 | intron-variant | USP36 | GRCh38.p7 | 17:78813760 | TCATCTGGGGAGGGC[A/G/T]TGAGTTTATTACCGC | 57602 |
rs200048059 | in-del | -/T | 0.0551013 | 0.156571 | intron-variant | USP36 | GRCh38.p7 | 17:78792713 | ATCCCCCCGGGAAGG[-/T]TTTTTTTTGTTGTCG | 57602 |
rs200096887 | snp | A/G/T | 0.000115704 | 0.00760526 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836063 | AAGTCCATCCACTTC[A/G/T]TCACCCCGGAGTGAG | 57602 |
rs200106464 | in-del | -/AT | 0.0376037 | 0.131863 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786935 | CAGAGGTAACCCAAA[-/AT]ATGTTTTTCCTATGC | 57602 |
rs200106890 | snp | C/G/T | 0.00039569 | 0.0140603 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803476 | TGCTCGCGTGGTGGC[C/G/T]GTCCGTAACACATCC | 57602 |
rs200126460 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808149 | TTCTAGTGCTTTCTT[G/T]TTTCAATCTTTTCTT | 57602 |
rs200128056 | snp | C/T | 0.00119659 | 0.0244307 | intron-variant | USP36 | GRCh38.p7 | 17:78828882 | ACAAAAATTTTAACA[C/T]GGATTGATGCTTACT | 57602 |
rs200128836 | snp | C/T | 0.000974727 | 0.0220548 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802354 | GACACCAGCCATTCG[C/T]GGATGGTGCGCAGCT | 57602 |
rs200160079 | snp | G/T | 6.63086e-05 | 0.0057576 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807500 | TGGGAGAGTTTGGGG[G/T]AAGGGGACCCCGAGG | 57602 |
rs200191789 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | USP36 | GRCh38.p7 | 17:78818633 | GCCGACTGTGGCCCA[C/T]GGAGCTGCCTGGGAT | 57602 |
rs200200290 | snp | A/G | 0.000842286 | 0.0205045 | intron-variant | USP36 | GRCh38.p7 | 17:78798863 | TCTGAGCTGAGCCAC[A/G]CCGCCCTGCTCCCTC | 57602 |
rs200221326 | in-del | -/ACAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815932 | CGCACACATACACAC[-/ACAT]ATACACACATGCATG | 57602 |
rs200234804 | snp | A/G | 0.000428287 | 0.0146274 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821938 | ACGTCTCCACTTACC[A/G]CGTGATCTGAGATAC | 57602 |
rs200248709 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78805217 | TCTAAACAAACTATA[A/C]GGGCCATGCCAGCTG | 57602 |
rs200263600 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816159 | AAAACATACGCATAA[-/T]TTTTTTTTTTTTTTT | 57602 |
rs200277148 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | USP36 | GRCh38.p7 | 17:78835755 | GGACACAGCTCAGAG[-/A]ACTGAGTGGCGGAAG | 57602 |
rs200286399 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP36 | GRCh38.p7 | 17:78810152 | TAGACAAGGTCTCAC[C/T]CTGTCACCTTGCCTG | 57602 |
rs200324254 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802472 | CTGCTTTCTTTTTTT[C/T]TTTTTCTTTTTCCTT | 57602 |
rs200324750 | snp | C/T | 0.000411879 | 0.0143447 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818773 | GCTGGAACCTTCTTC[C/T]TGCATCTATGAAGAA | 57602 |
rs200340355 | snp | A/T | 0.159292 | 0.232964 | intron-variant | USP36 | GRCh38.p7 | 17:78804691 | AAGTCAAAAAAAAAA[A/T]TTTTTTTTTTTTAAA | 57602 |
rs200405634 | snp | A/G | 0.000181919 | 0.00953553 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799743 | CCGCTCTCCATTCCA[A/G]GACACAGGAGGGGCC | 57602 |
rs200421297 | snp | C/T | 3.29935e-05 | 0.00406149 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836089 | GTGAGGGCCTCTCTG[C/T]CAGCACACTGCACAT | 57602 |
rs200421768 | snp | A/C/G | 4.95907e-05 | 0.00497929 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799730 | CCACATCAGACTCCC[A/C/G]CTCTCCATTCCAAGA | 57602 |
rs200423499 | snp | C/T | 4.95708e-05 | 0.00497825 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807453 | CCTTCTTTCCAGGGT[C/T]GTCTAGGATGGTTGG | 57602 |
rs200433292 | in-del | -/TATATATATT | | | intron-variant | USP36 | GRCh38.p7 | 17:78821413 | ATATATATATATATA[-/TATATATATT]TTTTTTTTTTTTTTT | 57602 |
rs200494132 | snp | C/G | 0.00199806 | 0.0315442 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835284 | CCCACACTCACAGCT[C/G]CGAGCATGCTCCTTG | 57602 |
rs200504456 | snp | A/G | 0.00199806 | 0.0315443 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812953 | GGGAAGGGAGGAGGA[A/G]CCTGTCCTGGAGATG | 57602 |
rs200528045 | snp | A/C/G | 0.000247072 | 0.0111121 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798947 | CCAGTCATCAACCAC[A/C/G]GTCTCAGTCCGGGCC | 57602 |
rs200547470 | snp | C/T | 0.000190096 | 0.0097474 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802334 | CATACCCATGCGGTC[C/T]CCAGGACACCAGCCA | 57602 |
rs200549451 | snp | A/C | 1.67142e-05 | 0.00289081 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835416 | GAAGACCCGCTCCCA[A/C]CTCAGAGACAGTCGC | 57602 |
rs200588002 | snp | A/C/G/T | 0.000181209 | 0.0095172 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812934 | GAATCACACTCGGGC[A/C/G/T]GCCGGGAAGGGAGGA | 57602 |
rs200623352 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840807 | CCGCGGCCCAGCACG[A/G]GCACCATCCGGGCCT | 57602 |
rs200626859 | snp | C/T | 0.000233696 | 0.0108071 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807237 | TCCTGTCGAGGCCAG[C/T]GCTCTCGTCGTTCCC | 57602 |
rs200647406 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802951 | ATTTTTTCTTTTTTC[-/T]TTTTTTTTAGACAGG | 57602 |
rs200685640 | snp | A/G | 1.65307e-05 | 0.0028749 | intron-variant | USP36 | GRCh38.p7 | 17:78813724 | GCCCACCGGTATAAG[A/G]AAAGAGCAGAGGGAG | 57602 |
rs200774801 | snp | A/G | 0.000181262 | 0.00951832 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807083 | TCTGCTCCACTTGGC[A/G]GCGTTTTGGAGTGGC | 57602 |
rs200828862 | in-del | -/T | 0.0155524 | 0.0868004 | intron-variant | USP36 | GRCh38.p7 | 17:78810154 | GACAAGGTCTCACTC[-/T]GTCACCTTGCCTGGA | 57602 |
rs200860990 | snp | C/T | 6.7348e-05 | 0.00580254 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807537 | TTGGAGGAATGCAGC[C/T]GTTCTGGGACTTCAG | 57602 |
rs200900561 | snp | C/G | 1.66813e-05 | 0.00288797 | intron-variant | USP36 | GRCh38.p7 | 17:78806948 | CAGCGGCGAGACCCC[C/G]ACACACCCACCTTCT | 57602 |
rs200900620 | in-del | -/AA | 0.310878 | 0.242475 | intron-variant | USP36 | GRCh38.p7 | 17:78804496 | AACAAAAACAAAAAC[-/AA]AAAAAAAAAAACAAA | 57602 |
rs200912475 | in-del | -/AT | 0.0178098 | 0.0926698 | intron-variant | USP36 | GRCh38.p7 | 17:78815829 | TACACACATGCACAC[-/AT]ATATACATACACACA | 57602 |
rs200931644 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831279 | AATATTGAAGAGCTC[-/T]TTTTTTTTCCAAAAC | 57602 |
rs200961471 | snp | C/T | 0.000149772 | 0.00865236 | intron-variant | USP36 | GRCh38.p7 | 17:78806335 | TCTAAAAAAGGTTTC[C/T]GTGAGTGAAGAGGGA | 57602 |
rs200980044 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78813271 | CACCAGAAAGCAAGA[A/C]CCTCAAACACCTCAG | 57602 |
rs201003428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828849 | CATCTCTACAAAAAA[C/T]TAAAAAATAAATAAA | 57602 |
rs201013812 | snp | A/G | 5.28471e-05 | 0.00514011 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802391 | CTCGGGGACAACAGC[A/G]TCTTGGGGCTTGGCA | 57602 |
rs201074072 | snp | A/G | 0.00017404 | 0.00932683 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803872 | TGGAGGAGCAGCTCC[A/G]TGGTTCTGACGTCCC | 57602 |
rs201086503 | snp | A/G | 0.00185989 | 0.0304383 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821006 | CCGGATCTCCAGCGC[A/G]ACGTCCAAGTAGGGG | 57602 |
rs201105873 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789039 | TCCGTCTCTATTAAA[A/G]TATGAAAATTAGCCG | 57602 |
rs201115350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826154 | GAGAAGGGGAAGAAC[A/G]CGTGACCAAACCCTC | 57602 |
rs201177319 | snp | C/T | 4.78446e-05 | 0.00489081 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821003 | TACCCGGATCTCCAG[C/T]GCGACGTCCAAGTAG | 57602 |
rs201194252 | snp | C/G/T | 0.000675269 | 0.0183629 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798424 | CAGGGGCACAGTCAG[C/G/T]GGCGATAGCTGAGGC | 57602 |
rs201229606 | snp | C/T | 0.0127969 | 0.0789601 | intron-variant | USP36 | GRCh38.p7 | 17:78810153 | AGACAAGGTCTCACT[C/T]TGTCACCTTGCCTGG | 57602 |
rs201281587 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798548 | ATTTTTTAATTTTCT[C/T]TTCCTAGACCAAGAA | 57602 |
rs201284395 | snp | A/C/T | 7.24e-05 | 0.00601627 | intron-variant | USP36 | GRCh38.p7 | 17:78829015 | CTGGTGGCCTGCCGG[A/C/T]GTGGAAGGAGGAGCA | 57602 |
rs201302268 | snp | A/C/G | 0.000199375 | 0.00998257 | missense, synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807184 | CTTGGTGGAGTCGCT[A/C/G]CTGGCCGAGTGCTCT | 57602 |
rs201313981 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78816175 | TTTTTTTTTTTTTTT[-/A]AAGAAACACAGTCTC | 57602 |
rs201317729 | snp | A/C | 3.29984e-05 | 0.00406179 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806261 | GGACGGAGGTCATTG[A/C]CGGTCGCCCTCCACA | 57602 |
rs201335912 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836142 | TGGGTCATCTCCACT[C/T]TTGTGGCGACTAGCT | 57602 |
rs201435693 | snp | C/T | 6.60055e-05 | 0.00574442 | intron-variant | USP36 | GRCh38.p7 | 17:78799664 | CTGTCTCCAAATCAG[C/T]ACCTTTTCTCCCGTA | 57602 |
rs201438220 | snp | C/T | 0.000230601 | 0.0107353 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798946 | CCCAGTCATCAACCA[C/T]GGTCTCAGTCCGGGC | 57602 |
rs201475167 | snp | A/G | 3.43737e-05 | 0.00414556 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803696 | CGCAGTGGCCTCCCT[A/G]ATGTGCTGTGGGAGG | 57602 |
rs201512075 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838387 | AAAAAAAAAAAAAAA[-/C]AAAAAACAAAAAACT | 57602 |
rs201517452 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817678 | AGAATCACTTGAACC[C/G]AGAAGGTGGAGACAG | 57602 |
rs201554834 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797875 | GACGCCTTGTCTCCA[A/G]GAGGCTGCAGAACAA | 57602 |
rs201571699 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78804680 | GTGATTTTAAAAGTC[-/A]AAAAAAAAAATTTTT | 57602 |
rs201618229 | snp | A/G | 5.03859e-05 | 0.005019 | intron-variant | USP36 | GRCh38.p7 | 17:78806940 | ATACACAGCAGCGGC[A/G]AGACCCCCACACACC | 57602 |
rs201654754 | snp | A/G | 0.00399203 | 0.0444981 | intron-variant | USP36 | GRCh38.p7 | 17:78814341 | TAAGTGCTCTACAGA[A/G]GCCGCATCTGGATGT | 57602 |
rs201659148 | snp | A/G | 0.000622723 | 0.0176344 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807538 | TGGAGGAATGCAGCC[A/G]TTCTGGGACTTCAGG | 57602 |
rs201663515 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819153 | AAGCAAAGCTAGAAG[A/T]TGCGCAAACACAGGG | 57602 |
rs201663556 | snp | A/G | 3.32729e-05 | 0.00407864 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803621 | CCCCTCCTGCAGGGC[A/G]CTGGCAGCTGTGTCC | 57602 |
rs201689153 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787952 | GGAGTGATGTGGCCA[G/T]AAGCCAAGGAATTCC | 57602 |
rs201766515 | snp | G/T | 1.65329e-05 | 0.0028751 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798547 | AATTTTTTAATTTTC[G/T]TTTCCTAGACCAAGA | 57602 |
rs201768892 | snp | C/G/T | 0.000609482 | 0.017448 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812929 | ATCTGGAATCACACT[C/G/T]GGGCGGCCGGGAAGG | 57602 |
rs201774114 | snp | C/T | 4.95078e-05 | 0.00497508 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828948 | CGTTGCCGCTGTTGG[C/T]GAAGGCCTGGACAAT | 57602 |
rs201824672 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790298 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTAAAGAC | 57602 |
rs201857791 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78801807 | GAGAAGCTGTAGACA[C/G]AACAGCTTTGAATCG | 57602 |
rs201928819 | snp | A/C | 0.000148776 | 0.00862357 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798546 | AAATTTTTTAATTTT[A/C]TTTTCCTAGACCAAG | 57602 |
rs201961301 | snp | A/G | 0.000421815 | 0.0145165 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835435 | AGAGACAGTCGCTCC[A/G]TGGGGAAAAGCACTT | 57602 |
rs202045817 | in-del | -/C | 0.0520825 | 0.152737 | intron-variant | USP36 | GRCh38.p7 | 17:78838380 | GGTCTCAAAAAAAAA[-/C]AAAAAACAAAAAACA | 57602 |
rs202054047 | snp | G/T | 0.000455539 | 0.0150852 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803647 | TGTCCTCCGGGCGCT[G/T]CTTCTTCTTCCTCTT | 57602 |
rs202089733 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78813270 | GCACCAGAAAGCAAG[-/A]ACCTCAAACACCTCA | 57602 |
rs202103052 | snp | C/T | 4.94262e-05 | 0.00497098 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818767 | TTGCTGGCTGGAACC[C/T]TCTTCTTGCATCTAT | 57602 |
rs202145006 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP36 | GRCh38.p7 | 17:78810154 | GACAAGGTCTCACTC[C/T]GTCACCTTGCCTGGA | 57602 |
rs202165617 | snp | A/C/T | 0.00335023 | 0.0407914 | intron-variant | USP36 | GRCh38.p7 | 17:78812824 | GTGAGGAGCACCAAG[A/C/T]CCAGCCACTTTGGCC | 57602 |
rs202229362 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815837 | TGCACACATATATAC[-/AT]ACACACACACATATG | 57602 |
rs367589918 | snp | G/T | 0.000115307 | 0.00759211 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818743 | GATGTTCTGTGGATG[G/T]TGAAGCGCTTGCTGG | 57602 |
rs367592381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789840 | CGCAGAAAAACAAAG[C/G]GGGTGCGGGTAGGGC | 57602 |
rs367602203 | snp | C/G | 0.000164886 | 0.00907831 | intron-variant | USP36 | GRCh38.p7 | 17:78798385 | CACCCTTACACCCAC[C/G]CCCTCGGAACCGACC | 57602 |
rs367608403 | snp | G/T | 1.65367e-05 | 0.00287543 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835381 | GTGTTGCCAAGGTTG[G/T]GGAGTCCTGCGCCCA | 57602 |
rs367628011 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805767 | AAACGCTCGGGACTC[C/T]GAGCTCACTCAAGCC | 57602 |
rs367639274 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811732 | AATTAGCCATGCATG[C/G]TGGCACACGCCTGTA | 57602 |
rs367725029 | snp | C/T | 2.02755e-05 | 0.00318392 | intron-variant, splice-acceptor-variant | USP36 | GRCh38.p7 | 17:78802539 | ATGGGAGAGCAGCTG[C/T]TTGGAAGTGAGAGGC | 57602 |
rs367735053 | snp | A/C/G | 1.65416e-05 | 0.00287586 | intron-variant | USP36 | GRCh38.p7 | 17:78799628 | CCTACAAAACCAACC[A/C/G]ATGAAAGGCAAACAG | 57602 |
rs367739793 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP36 | GRCh38.p7 | 17:78821064 | ACGGAGCACTTCACT[A/G]CAACAGAACAGAGGC | 57602 |
rs367823832 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807783 | TCTGGACTCTTGGTA[A/G]AGACACTGTGGCTTC | 57602 |
rs367873011 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811886 | GAAAAAAAAAAAAGG[A/G]TATTTTTTCCTACAC | 57602 |
rs367924009 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78811740 | ATGCATGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 57602 |
rs367953812 | snp | C/T | 4.95242e-05 | 0.0049759 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807362 | CTCCCAGATCTGCTG[C/T]TATTCGAGTTGCTGG | 57602 |
rs367981815 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78805756 | CGTCCCACAAAAAAC[A/G]CTCGGGACTCCGAGC | 57602 |
rs368052548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789639 | GCTAAAGCTTGCAAT[C/T]TCTTCTGTGTGTAAA | 57602 |
rs368065522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815983 | ACACACATATAATAC[A/G]TGCACACACATATAT | 57602 |
rs368069349 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801125 | GGGACTAGAGGCGCC[C/T]GCCACCATGCCTGGC | 57602 |
rs368071453 | snp | C/T | 6.74184e-05 | 0.00580557 | intron-variant | USP36 | GRCh38.p7 | 17:78806939 | GATACACAGCAGCGG[C/T]GAGACCCCCACACAC | 57602 |
rs368110088 | snp | A/G | 1.69896e-05 | 0.00291454 | intron-variant | USP36 | GRCh38.p7 | 17:78814580 | TCAAGGAAAAGACAA[A/G]TAAAATTCACTTTGA | 57602 |
rs368202512 | snp | C/T | 0.000172414 | 0.00928317 | intron-variant | USP36 | GRCh38.p7 | 17:78835551 | AGACGTAAGTCCACA[C/T]ACAGGTCGTCCACAA | 57602 |
rs368230256 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816667 | TTTTTTGTAGAGACA[G/T]GGTCTCACTATGTTG | 57602 |
rs368231044 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818349 | GACTGTGTATAACAA[A/G]CATTCAGGGATTTTG | 57602 |
rs368262130 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78840236 | AGCCCCAGGCCCAGG[A/G]CCCCCACGCCACCCG | 57602 |
rs368272699 | snp | C/T | 3.32541e-05 | 0.00407749 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807511 | GGGGGAAGGGGACCC[C/T]GAGGGCAGCTTTGGA | 57602 |
rs368289230 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798956 | AACCACGGTCTCAGT[C/T]CGGGCCTGTCTGCTG | 57602 |
rs368384620 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78815830 | ACACACATGCACACA[C/T]ATATACATACACACA | 57602 |
rs368388383 | snp | A/G | 4.94466e-05 | 0.00497201 | intron-variant | USP36 | GRCh38.p7 | 17:78818657 | CTGGGATGGTGTCAC[A/G]AGCGCTCACCTTGGT | 57602 |
rs368490008 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78788767 | ATCATCTACGGCCTC[A/C]CCTCCACCAAGGGGA | 57602 |
rs368537697 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817363 | TGCTGACCTAAGCAA[A/G]CCCCCACCACTACCA | 57602 |
rs368552550 | snp | A/G | 1.76786e-05 | 0.00297305 | intron-variant | USP36 | GRCh38.p7 | 17:78803360 | CGTCAGAGGTAGACA[A/G]ATGCCACTTTGCTCC | 57602 |
rs368566844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830446 | TTTTCTCTGCTATCA[C/T]AGACATTTTGCAATG | 57602 |
rs368569506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815928 | CATACGCACACATAC[A/G]CACACATATACACAC | 57602 |
rs368571455 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78797921 | ACAGAGAGAAACGAG[A/G]CCCGAATCTTCCCAC | 57602 |
rs368577222 | in-del | -/CACACATA | | | intron-variant | USP36 | GRCh38.p7 | 17:78815844 | ATATATACATACACA[-/CACACATA]TGCATGCATACACAT | 57602 |
rs368705721 | snp | A/G | 0.00551974 | 0.0522437 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802355 | ACACCAGCCATTCGC[A/G]GATGGTGCGCAGCTG | 57602 |
rs368742664 | snp | A/G | 4.98691e-05 | 0.0049932 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821034 | GGGTCGTAGGTGTCC[A/G]AGACGCTCTTGCACA | 57602 |
rs368745771 | snp | A/G | 6.58935e-05 | 0.00573955 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798999 | TCCTGACTGACCGCC[A/G]ACATCTTGCCATCCC | 57602 |
rs368770318 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802961 | TTTTCTTTTTTTTTA[C/G]ACAGGGTTTAGCTGT | 57602 |
rs368778432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78806674 | TCGGGTTCAGTCAGG[A/G]TCTTCCACCTACTGT | 57602 |
rs368781588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78792284 | GGGAAGAGTGAGACA[C/T]GGGAGCAGACAGGGT | 57602 |
rs368894252 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78821238 | TCTTTCACCACTGAA[A/G]TTCACAAAGATGGAT | 57602 |
rs368898881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789749 | GCTGGCCACGTGCCA[C/T]GGTTTGGGCGTTCAC | 57602 |
rs368954783 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812933 | GGAATCACACTCGGG[C/T]GGCCGGGAAGGGAGG | 57602 |
rs368958421 | snp | A/G | 9.89593e-05 | 0.00703348 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807116 | GCGGTGGAACAGTTC[A/G]TTTCCTGAGAATCGC | 57602 |
rs368971497 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831204 | GCACTCCGGCCTGGG[C/T]GACAGAGTGAAACTC | 57602 |
rs369008166 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78802942 | AGAGGAGATATTTTT[-/TC]TTTTTTCTTTTTTTT | 57602 |
rs369042594 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812606 | AGGCAGGAGAATGGC[-/G]GGGAACCCGGGAGGC | 57602 |
rs369064069 | snp | A/G | 1.65018e-05 | 0.00287239 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828917 | AGGTCTCGGATGAAG[A/G]AGACGGGCTTGATGG | 57602 |
rs369086826 | snp | C/T | 3.7991e-05 | 0.00435822 | intron-variant | USP36 | GRCh38.p7 | 17:78813925 | TCAACAAGCATCCCA[C/T]TATCCTCACTTTTTA | 57602 |
rs369098312 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836175 | CTCTGTTTTGGGGTT[G/T]AGCAACACATATTTG | 57602 |
rs369124500 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78820373 | TACCAGCTGTGTGGG[A/G]GGATCACTTAAGCCT | 57602 |
rs369144215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78812683 | GCCTGGATGACAGAG[C/T]GAGACTCTGTCTCGA | 57602 |
rs369154381 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822068 | CGAGGGATGGCCCCA[A/T]CCCAGCAGCCCCATG | 57602 |
rs369166543 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791237 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 57602 |
rs369280197 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802606 | AGCGCACAGACACCC[A/C/G]CCTGCAACATGGAGA | 57602 |
rs369303458 | snp | A/C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806602 | CCCACTGGGGCTCTG[A/C/T]GCTTCCTGCCCGCCC | 57602 |
rs369328841 | in-del | -/ACGGTGGG | | | intron-variant | USP36 | GRCh38.p7 | 17:78789920 | CACTGACTTTGATGG[-/ACGGTGGG]CTGGCTGTTTTCTGA | 57602 |
rs369337220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78818223 | CAATGCAAGTCCCAC[C/T]GCCCAGTGCTCATCA | 57602 |
rs369343127 | snp | C/T | 4.94262e-05 | 0.00497098 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836185 | GGGTTGAGCAACACA[C/T]ATTTGCTCTTTAAGG | 57602 |
rs369353557 | snp | A/G | 4.968e-05 | 0.00498373 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807163 | ACTCCTGGGGGTCTG[A/G]GGGGCCTTGGTGGAG | 57602 |
rs369371363 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78813385 | CAGGAGAAGGCCCCT[C/T]CAGAGAAGCTCTGCA | 57602 |
rs369403300 | snp | A/C | 0.000697757 | 0.0186653 | intron-variant | USP36 | GRCh38.p7 | 17:78798368 | CACACACACCCCCAC[A/C]TCACCCTTACACCCA | 57602 |
rs369404575 | in-del | -/CTCG | | | intron-variant | USP36 | GRCh38.p7 | 17:78810151 | TAGACAAGGTCTCAC[-/CTCG]TCTGTCACCTTGCCT | 57602 |
rs369434720 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798433 | AGTCAGCGGCGATAG[C/T]TGAGGCTGGCAGCCT | 57602 |
rs369463937 | snp | A/G | 0.00080949 | 0.020102 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802379 | GCAGCTGCTGGACTC[A/G]GGGACAACAGCATCT | 57602 |
rs369473181 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825740 | TTCTGTCCTAAGAGC[A/G]CTCCAGGTGGCTGCA | 57602 |
rs369478839 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838394 | AAAAAAAACAAAAAA[A/C]AAAAAACTTCTGTAA | 57602 |
rs369498906 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837897 | ATCTAATTCTATACA[C/T]GGATCAAGTATCTTT | 57602 |
rs369534540 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821989 | CAAGGTAGTAGCCTG[C/T]GTTTGACGATCCAAC | 57602 |
rs369562349 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795873 | CAAGCACAAAATTCA[A/G]CAGACCCAGATCCTA | 57602 |
rs369579678 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802973 | TTAGACAGGGTTTAG[C/G]TGTCACCCAGGCTGT | 57602 |
rs369584125 | snp | A/G/T | 3.30089e-05 | 0.00406246 | missense, synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798531 | CCTCTTCTCTCTCTT[A/G/T]AATTTTTTAATTTTC | 57602 |
rs369599195 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835483 | CCGTCACCACAGCTC[C/T]CATACGTGTGCTCAC | 57602 |
rs369599902 | snp | A/C | 1.651e-05 | 0.0028731 | intron-variant | USP36 | GRCh38.p7 | 17:78819882 | CAGGTGAGGGGACTT[A/C]TTTCCCGTCTGGTAT | 57602 |
rs369603546 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806978 | TTGGCAGAAAGGGCC[A/G]GTTTTTTGGCTGGTG | 57602 |
rs369604331 | snp | A/C | 1.65176e-05 | 0.00287376 | intron-variant | USP36 | GRCh38.p7 | 17:78818796 | ATGAAGAAGGTGATG[A/C]GAAAGATTAATGAAT | 57602 |
rs369673478 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78810382 | AGCCTTAATCTCCCT[A/G]GCTCAAGTGATCCTC | 57602 |
rs369770421 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795290 | GTCCAGCCAAACCCC[A/T]AAAGAGAAGCGAAGA | 57602 |
rs369774514 | in-del | -/ATAT | 0.0471551 | 0.14613 | intron-variant | USP36 | GRCh38.p7 | 17:78815849 | TACATACACACACAC[-/ATAT]GCATGCATACACATG | 57602 |
rs369804184 | snp | C/T | 6.73015e-05 | 0.00580054 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803643 | GCTGTGTCCTCCGGG[C/T]GCTTCTTCTTCTTCC | 57602 |
rs369815604 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819633 | CCCATGGCTGGTCAC[C/T]TCACTTCTCTGTGCC | 57602 |
rs369845728 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808418 | ACCACACCCGAATAA[C/T]TATTACTATTTTGTA | 57602 |
rs369863151 | in-del | -/TGAGGCAGAATC | | | intron-variant | USP36 | GRCh38.p7 | 17:78793698 | CAAGCTACCAAGACT[-/TGAGGCAGAATC]TGAGGCAGGGATTCT | 57602 |
rs369890156 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812719 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAATA | 57602 |
rs370005121 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820255 | CGGGGCAGGAGGATC[A/T]TTGAGGCCAGGAGTT | 57602 |
rs370005760 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838605 | GGATGTGCAGACTTG[A/G]GCCTGCTGTCCTACT | 57602 |
rs370008283 | snp | C/T | 0.000280045 | 0.0118298 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806169 | ACCTGGCTCTATGGA[C/T]GGGCCAAGTGGAGGC | 57602 |
rs370089975 | snp | C/T | 0.000231554 | 0.0107575 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827329 | TCCTGGTTCCCAAAG[C/T]GGAAGTGTCGGGCGA | 57602 |
rs370094599 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803580 | TCCCTCCTGTACATG[A/G]GGCTCCCAGGCTGTC | 57602 |
rs370137888 | snp | C/T | 3.33834e-05 | 0.00408541 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807282 | CGTTGGCAGTGGCTG[C/T]AGCCAGGAGCTTAGG | 57602 |
rs370186283 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822653 | GCCTCTTCTCACCCG[C/G]ACCCGGGGCTGCCTG | 57602 |
rs370225999 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78833950 | GAATTGTTTCTTAAA[A/C]GTTACATAGAAATTG | 57602 |
rs370226306 | snp | A/G | 3.32773e-05 | 0.00407892 | intron-variant | USP36 | GRCh38.p7 | 17:78812821 | TCTGTGAGGAGCACC[A/G]AGACCAGCCACTTTG | 57602 |
rs370230515 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | USP36 | GRCh38.p7 | 17:78819900 | TCCCGTCTGGTATCA[C/G]TCTTCTGCCACAAGC | 57602 |
rs370254525 | snp | A/G/T | 0.00021662 | 0.0104054 | intron-variant | USP36 | GRCh38.p7 | 17:78827219 | GGTGTCCAAAGCCCT[A/G/T]GGAGGGTGGGTGGGG | 57602 |
rs370357338 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814503 | ACAGGATCACCATTA[C/T]TCTGGGACATATACG | 57602 |
rs370429988 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792976 | CCGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 57602 |
rs370434657 | snp | C/T | 0.00025792 | 0.0113531 | intron-variant | USP36 | GRCh38.p7 | 17:78802314 | TCCCACCCCCTCGCC[C/T]GGTGCATACCCATGC | 57602 |
rs370485135 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806165 | GCTTACCTGGCTCTA[C/T]GGACGGGCCAAGTGG | 57602 |
rs370520662 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816124 | TGGGTCATATACAGA[C/T]GTGTGTTTAGGAACT | 57602 |
rs370522648 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834580 | GCCTCCCGAGCAGCT[G/T]GGATTACAGGTGCAC | 57602 |
rs370608140 | snp | A/G | 4.94499e-05 | 0.00497217 | intron-variant | USP36 | GRCh38.p7 | 17:78819919 | TCTGCCACAAGCAAC[A/G]TGAAACTTACTTAGC | 57602 |
rs370614897 | snp | A/G | 1.8447e-05 | 0.00303696 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803947 | AGGGGGGTTGCAGGC[A/G]GCTGGATGATTGGGG | 57602 |
rs370615657 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798923 | CTTCCCTCGGTCAAA[C/T]TCTTCGTCCCAGTCA | 57602 |
rs370711931 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810665 | CTGCCACTTCAATTC[C/T]AATGCTTCTAATTTC | 57602 |
rs370715473 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796550 | AGACACCCACCCACA[C/T]GGAAAAAAATAAATG | 57602 |
rs370724993 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78820644 | GCGACAAAGCCAAGG[A/C]TGCTCTCCCAGGTGA | 57602 |
rs370736827 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820191 | AGACAAGAAATGAAA[A/G]CAGCCAGGAACAGCG | 57602 |
rs370777524 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78829088 | CACCCCAAACGTTAA[C/T]ACAGCCAGAAACACA | 57602 |
rs370790521 | snp | A/G | 3.127e-05 | 0.00395399 | intron-variant | USP36 | GRCh38.p7 | 17:78820963 | TCGCTCTCCTACTGC[A/G]AAAGTGAAGGGCAGG | 57602 |
rs370800443 | snp | C/T | 0.0014412 | 0.0268052 | intron-variant | USP36 | GRCh38.p7 | 17:78818620 | GTGTTATTCTGATGC[C/T]GACTGTGGCCCACGG | 57602 |
rs370803180 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798970 | TCCGGGCCTGTCTGC[C/T]GTCTTCAATAGCATC | 57602 |
rs370835613 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78804671 | AAGCCAACACGTGAT[G/T]TTAAAAGTCAAAAAA | 57602 |
rs370913457 | snp | C/G/T | 5.73963e-05 | 0.00535681 | intron-variant | USP36 | GRCh38.p7 | 17:78835263 | CAGCCACCCCACTGC[C/G/T]GCAAACCCACACTCA | 57602 |
rs370937412 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829460 | GTGCCTCAGATATGG[A/G]ACCGTCTGTTCCACT | 57602 |
rs370981846 | snp | G/T | 8.26221e-05 | 0.00642684 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806279 | GTCGCCCTCCACAGG[G/T]TGCTGGCCTGCAGTT | 57602 |
rs371038647 | snp | G/T | 0.000270684 | 0.0116305 | intron-variant | USP36 | GRCh38.p7 | 17:78807679 | CTGAGGAAGCGAGAA[G/T]TCTCAGCTGGGCCAC | 57602 |
rs371055257 | in-del | -/AAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78830890 | TTTTAAAATGACAAT[-/AAT]GATTGGTGAACTCAA | 57602 |
rs371063116 | snp | A/G | 5.59707e-05 | 0.00528982 | intron-variant | USP36 | GRCh38.p7 | 17:78835522 | GAAGAAAGGGACAAG[A/G]GAAGAAAAGAGGAAG | 57602 |
rs371093651 | snp | C/G | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807345 | AGGAGCCCTGCCTTT[C/G]GCTCCCAGATCTGCT | 57602 |
rs371250301 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | USP36 | GRCh38.p7 | 17:78802586 | CAAATTGGAAGGGGA[A/G]CAGGAGCGCACAGAC | 57602 |
rs371268256 | snp | C/T | 0.000116441 | 0.00762933 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807190 | GGAGTCGCTGCTGGC[C/T]GAGTGCTCTGGGCTG | 57602 |
rs371298766 | in-del | -/TCCCCTGGATCAGTGA | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836481 | AGCCACCACAAAAGC[-/TCCCCTGGATCAGTGA]TCCCCTGGATCAGCT | 57602 |
rs371311979 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78813275 | AGAAAGCAAGAACCT[A/C]AAACACCTCAGCCAC | 57602 |
rs371313596 | snp | A/G | 8.24137e-05 | 0.00641873 | intron-variant | USP36 | GRCh38.p7 | 17:78799043 | CAGGCAGACACGGGG[A/G]TCAGCACGAGTGCAG | 57602 |
rs371339600 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78825992 | TACACCATGAGCTCC[A/T]CAGACTCCAGGACCA | 57602 |
rs371423258 | snp | C/T | 4.94262e-05 | 0.00497098 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818766 | CTTGCTGGCTGGAAC[C/T]TTCTTCTTGCATCTA | 57602 |
rs371428435 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78798247 | GACACACACCACAGA[C/T]GCGCCCACACCACAC | 57602 |
rs371428551 | snp | A/G | 4.94539e-05 | 0.00497238 | intron-variant | USP36 | GRCh38.p7 | 17:78798391 | TACACCCACCCCCTC[A/G]GAACCGACCTCCTTC | 57602 |
rs371440288 | snp | C/T | 1.66172e-05 | 0.00288242 | intron-variant | USP36 | GRCh38.p7 | 17:78798595 | TCCCAAAAACGGCTC[C/T]TTCCTGGCCCACGGG | 57602 |
rs371461948 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825110 | ACAAGAGCACATGGA[C/T]ATAGAAAATGAAAAC | 57602 |
rs371515308 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835406 | CGCCCACGCGGAAGA[C/T]CCGCTCCCACCTCAG | 57602 |
rs371566707 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837761 | CTTCCTCTGGTATTC[A/T]GTACCCAGCCTGCCC | 57602 |
rs371598672 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842770 | CAATACAACTATTCT[A/G]TTAATGCACCTTTTT | 57602 |
rs371645037 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837964 | GTGGCCTGGGCCTGT[C/T]GTCCCAGATGCTTGG | 57602 |
rs371651436 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78826139 | CTTGAGCCCCTTCAG[C/G]AGAAGGGGAAGAACG | 57602 |
rs371761522 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805960 | CCGAACTGCCTTCAC[C/T]ACCCAAAGCTCCTTT | 57602 |
rs371805089 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817716 | GCAATCCAGCCTGGG[C/G/T]ATCAGAGCAAGACTC | 57602 |
rs371913112 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802034 | CAGATGCAGTAGACG[-/G]CTGCTCTCAGCCTGT | 57602 |
rs371941904 | snp | A/C | 9.52487e-05 | 0.00690038 | intron-variant | USP36 | GRCh38.p7 | 17:78821068 | AGCACTTCACTGCAA[A/C]AGAACAGAGGCAGTG | 57602 |
rs372037379 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78800134 | AAAAAGCTAAAAACC[-/A]AAAAAAAAAAAAACC | 57602 |
rs372088433 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | USP36 | GRCh38.p7 | 17:78818661 | GATGGTGTCACGAGC[A/G]CTCACCTTGGTGATC | 57602 |
rs372123422 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805587 | ACCAGTTACTCTCAA[C/T]TTCCTGCCACTCGAG | 57602 |
rs372123606 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789982 | GTATGCTGCCTTCAG[C/T]AGCTGCTCCAGTTCA | 57602 |
rs372124398 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790131 | TCTCGCTCTGTCATC[C/T]AGGCTGGAGTGCAAT | 57602 |
rs372219044 | snp | C/T | 0.000115351 | 0.00759355 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807082 | ATCTGCTCCACTTGG[C/T]GGCGTTTTGGAGTGG | 57602 |
rs372254201 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821253 | GTTCACAAAGATGGA[C/T]GTCAATATCTTTGCA | 57602 |
rs372356830 | snp | C/G/T | 0.000147617 | 0.00859003 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835455 | GAAAAGCACTTTCTG[C/G/T]GGGGCTGGGACTCCG | 57602 |
rs372368137 | snp | C/G | 0.000953887 | 0.0218182 | intron-variant | USP36 | GRCh38.p7 | 17:78806944 | ACAGCAGCGGCGAGA[C/G]CCCCACACACCCACC | 57602 |
rs372374583 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP36 | GRCh38.p7 | 17:78821584 | AGGCATGTGCCACCG[C/T]GCCTGGCTGATTTTT | 57602 |
rs372416751 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816175 | TTTTTTTTTTTTTTT[-/T]AAGAAACACAGTCTC | 57602 |
rs372489967 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792390 | GGGGCACCTCGTCCA[A/G]CATCTCCAGTAGAGG | 57602 |
rs372508678 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78823687 | GGCATGGGCTCTCAG[G/T]GGGAGAAGGCAAAGA | 57602 |
rs372509099 | snp | C/T | 5.10399e-05 | 0.00505147 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803391 | TGCCCTTACCTGTGC[C/T]GAAGTGGGTCCTGGT | 57602 |
rs372522380 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822073 | GATGGCCCCATCCCA[A/G]CAGCCCCATGCCCAC | 57602 |
rs372550772 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788041 | TCTCTCTGGCACTGT[-/T]GAGAGAACATTCCCA | 57602 |
rs372564351 | snp | A/C/G | 0.000648147 | 0.0179908 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807512 | GGGGAAGGGGACCCC[A/C/G]AGGGCAGCTTTGGAG | 57602 |
rs372655939 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838728 | CTGTTCAAACACCGA[A/G]GCCGCAGAGCGGGCG | 57602 |
rs372665806 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809338 | TGTTTTGTTCCCTAC[A/G]TTCTATTCTTTGTTA | 57602 |
rs372667209 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78830711 | AATGCAACAGCATGC[A/T]GCCTGCTTAGCAAAT | 57602 |
rs372674733 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836178 | TGTTTTGGGGTTGAG[C/T]AACACATATTTGCTC | 57602 |
rs372695693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78831775 | TGCCTAACCAAATCT[C/T]TACCCAAAGAATACA | 57602 |
rs372703565 | snp | A/G | 8.23757e-05 | 0.00641725 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836125 | CCCTGTCTCCTGGCC[A/G]GTGGGTCATCTCCAC | 57602 |
rs372750913 | snp | A/G | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812977 | GGAGATGAGGCCCTC[A/G]GGACTTTTCTTAGAG | 57602 |
rs372753811 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78825634 | GCCCCAAATCCAAAC[C/T]GTTATTCATTCTACC | 57602 |
rs372776119 | snp | A/G | 6.59131e-05 | 0.0057404 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806191 | AGTGGAGGCAACGAC[A/G]GGGTGAGAGGTTTTC | 57602 |
rs372863390 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828767 | CCCAACACTTTGGCA[G/T]GCCAAAACGGAAGGA | 57602 |
rs372871604 | snp | C/G | 4.96134e-05 | 0.00498039 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836351 | CCTCCTTCAACTTAT[C/G]CACTATTGGCATGGT | 57602 |
rs372873518 | snp | A/G | 9.93131e-05 | 0.00704604 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807164 | CTCCTGGGGGTCTGG[A/G]GGGCCTTGGTGGAGT | 57602 |
rs372915088 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835378 | CAGGTGTTGCCAAGG[C/T]TGTGGAGTCCTGCGC | 57602 |
rs372935119 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794993 | AGCCTGGGCGACAGA[C/G]GGAGACTCTGTTCGG | 57602 |
rs372960800 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831384 | TTGGGAGGGTGAGGC[A/G]GGTGGAACACGTGAG | 57602 |
rs373002809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78810983 | GCCGGGAGTGCTGGC[A/G]GGCACCTGTAATTAC | 57602 |
rs373010970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78820403 | TAGAGGTCAACACTA[C/T]AGTGAGCTATGATTG | 57602 |
rs373034953 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824278 | AATGAAATCATGCAC[A/G]CTAAAATGGCAAGAG | 57602 |
rs373037489 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819116 | GGCTGAGTGATAAAA[C/T]GGGCAGGCAGGAAGT | 57602 |
rs373077121 | snp | C/T | 1.84333e-05 | 0.00303584 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807614 | GTGGTGTGCGGCTTC[C/T]TCATCGTCCCAGAGT | 57602 |
rs373108679 | snp | C/T | 1.65425e-05 | 0.00287593 | intron-variant | USP36 | GRCh38.p7 | 17:78818807 | GATGAGAAAGATTAA[C/T]GAATGATTGATTCGT | 57602 |
rs373179591 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78814053 | TCGGAATGTGACCCC[A/T]AAGTGTGCTCTGCGT | 57602 |
rs373193629 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799364 | GTGACATTACCCAGG[C/T]TGGAAGAGCTTCGTC | 57602 |
rs373221256 | snp | A/G | 1.70766e-05 | 0.00292199 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803727 | CGCGTCTCTGAGCCC[A/G]GCCTCTGCGGCTCTC | 57602 |
rs373263167 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828940 | CTTGATGGCGTTGCC[A/G]CTGTTGGCGAAGGCC | 57602 |
rs373304362 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78820040 | AAAACAGGGAGTAAA[A/C]TACACAGCAGAGGAA | 57602 |
rs373468063 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78798635 | TGCATGCAGGTCCTG[C/T]ACACAGGCCGGGCTC | 57602 |
rs373476773 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP36 | GRCh38.p7 | 17:78819917 | CTTCTGCCACAAGCA[A/C]CGTGAAACTTACTTA | 57602 |
rs373532629 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787752 | CAACAAAAGATATGT[G/T]GAAGTCCTAAGCCCC | 57602 |
rs373562267 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78815765 | TATGCATACATGCAC[A/G]CATAAAATACATGCA | 57602 |
rs373584408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78816492 | TTAGCCAAGCATGGT[A/G]GCACACATTTGTGGT | 57602 |
rs373613921 | snp | C/G | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798455 | TGGCAGCCTTTGCTG[C/G]GTGAGTCACAGACCA | 57602 |
rs373709321 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | USP36 | GRCh38.p7 | 17:78813737 | AGAAAAGAGCAGAGG[C/G]AGTGAGCTCATCTGG | 57602 |
rs373721234 | multinucleotide-polymorphism | GC/TT | | | intron-variant | USP36 | GRCh38.p7 | 17:78827094 | TTTGGGCTCCAACAG[GC/TT]TGAGTACCCAGAGGC | 57602 |
rs373789210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811673 | AGCAGATAGAGACCA[C/T]CCTGGCTAATAAAGT | 57602 |
rs373820856 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805616 | AGGCACCTAAGAGAC[A/G]CAGGCAGCCCCTGCG | 57602 |
rs373833822 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790064 | GAGAACTGTAGCCAC[A/G]TAAGACAGAAAAATG | 57602 |
rs373938196 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797425 | GCTGAGGAAGCAGGG[G/T]AGGGCGGGCTCGGAC | 57602 |
rs373944550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829853 | TTAAGCAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 57602 |
rs373998078 | snp | A/C | 4.94254e-05 | 0.00497094 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819959 | GGCATTCTCTCCACT[A/C]AGGACATCTGCTTTC | 57602 |
rs374046674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78803292 | ACGCAAGCAGACTAC[A/G]TTTCCAGACCATACC | 57602 |
rs374160880 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796562 | ACATGGAAAAAAATA[A/T]ATGTATCTTCCCATA | 57602 |
rs374191326 | snp | A/C | 0.0026653 | 0.036408 | intron-variant | USP36 | GRCh38.p7 | 17:78802295 | CGGTGCACACCCATG[A/C]GGTTCCCACCCCCTC | 57602 |
rs374232105 | snp | A/G | 3.91596e-05 | 0.00442474 | intron-variant | USP36 | GRCh38.p7 | 17:78827241 | TGGGTGGGGAAGCAC[A/G]CACTTGGCACAGCCA | 57602 |
rs374235197 | snp | C/T | 0.000342614 | 0.0130839 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802419 | GCACTCCTTGGGCAT[C/T]TGAGATGCCCATCCT | 57602 |
rs374268620 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789612 | GCTTTGAAAACCCCC[A/C]GATTTTATTTTGCTA | 57602 |
rs374320288 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807199 | GCTGGCCGAGTGCTC[C/T]GGGCTGGAGCTGCTG | 57602 |
rs374364136 | snp | C/T | 0.000165289 | 0.00908941 | intron-variant | USP36 | GRCh38.p7 | 17:78798862 | CTCTGAGCTGAGCCA[C/T]GCCGCCCTGCTCCCT | 57602 |
rs374377239 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823072 | CCCTCCCACAGAACA[G/T]GCACACCTCAGTCTC | 57602 |
rs374434340 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818875 | AGCAACAACTGCTCT[C/G]TAATAGTGGAATCTT | 57602 |
rs374448824 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841557 | GCGAAGGTTTTAGCT[G/T]AGTATTTGTGAGCAC | 57602 |
rs374487136 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78793028 | CCCCCCTCACCCCCC[A/C]AGGAAGGCTTTAAAT | 57602 |
rs374497941 | snp | C/T | 6.62603e-05 | 0.0057555 | intron-variant | USP36 | GRCh38.p7 | 17:78814404 | CTGCACTGACACAAG[C/T]CTCTCACCTTCACGT | 57602 |
rs374498969 | in-del | -/CT | 0.0115144 | 0.0749975 | intron-variant | USP36 | GRCh38.p7 | 17:78826958 | CTAACATATTTCCCC[-/CT]GACTGAGCTGCTCAG | 57602 |
rs374505941 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798988 | CTTCAATAGCATCCT[C/G]ACTGACCGCCGACAT | 57602 |
rs374510044 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78820212 | AGGAACAGCGGCTCA[C/T]GCCTATAATCCCAGC | 57602 |
rs374515037 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78825825 | GTGCTGGGGACACCG[A/C]AACCCTCCTCCTGGG | 57602 |
rs374583157 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820291 | CAAGCCTGGGCAACA[C/T]AGCAAGACCCCTGTC | 57602 |
rs374600237 | snp | C/T | 3.39472e-05 | 0.00411976 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835285 | CCACACTCACAGCTG[C/T]GAGCATGCTCCTTGG | 57602 |
rs374603235 | in-del | -/CA | | | intron-variant | USP36 | GRCh38.p7 | 17:78798243 | CTAGGACACACACCA[-/CA]GACGCGCCCACACCA | 57602 |
rs374646650 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835410 | CACGCGGAAGACCCG[C/T]TCCCACCTCAGAGAC | 57602 |
rs374675452 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78817724 | GCCTGGGCATCAGAG[A/C]AAGACTCTGTCTCAA | 57602 |
rs374683284 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802594 | AAGGGGAGCAGGAGC[A/G]CACAGACACCCGCCT | 57602 |
rs374714211 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78811862 | GACAGAATGAGACTC[A/C]GTCTCAAAGAAAAAA | 57602 |
rs374738308 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788833 | ACCAAGGCCAGAATG[C/T]TGCCTCTTGCCAGAG | 57602 |
rs374752914 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815866 | ATGCATGCATACACA[C/T]GTACGCATATACATA | 57602 |
rs374758208 | snp | C/T | 5.59874e-05 | 0.00529061 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803957 | CAGGCGGCTGGATGA[C/T]TGGGGAGCAGGTGAC | 57602 |
rs374966269 | snp | A/C/T | 9.9003e-05 | 0.00703516 | intron-variant | USP36 | GRCh38.p7 | 17:78813749 | AGGGAGTGAGCTCAT[A/C/T]TGGGGAGGGCGTGAG | 57602 |
rs375010260 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807297 | TAGCCAGGAGCTTAG[G/T]TGAGGTAGAGAGGAC | 57602 |
rs375015532 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78798151 | TGTATAAGGGGGTGT[A/G]TGTAGTGTGTGTTGG | 57602 |
rs375079416 | snp | A/C/G/T | 0.000197806 | 0.00994344 | intron-variant | USP36 | GRCh38.p7 | 17:78799053 | CGGGGGTCAGCACGA[A/C/G/T]TGCAGGTTCCCAGGT | 57602 |
rs375080552 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | USP36 | GRCh38.p7 | 17:78839486 | ACTCCCCACAATATC[A/T]CTGCTTTCGGTTAGG | 57602 |
rs375091394 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP36 | GRCh38.p7 | 17:78821458 | TTTGAGATAGAGTCT[C/T]GCTCTGTCACTCAGG | 57602 |
rs375216304 | snp | C/G/T | 0.000288414 | 0.0120053 | intron-variant | USP36 | GRCh38.p7 | 17:78814577 | AAATCAAGGAAAAGA[C/G/T]AAATAAAATTCACTT | 57602 |
rs375221323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802691 | CCCACACGCATTAGC[A/G]GACGCTCCACACGCA | 57602 |
rs375335141 | snp | C/T | 3.30546e-05 | 0.00406524 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807465 | GGTCGTCTAGGATGG[C/T]TGGCATGTGTGTGGG | 57602 |
rs375335757 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825238 | CTGGTCACCTATAAT[C/T]ACGGAGAAAACATCA | 57602 |
rs375343338 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842169 | TGGTGGGCGCCTGTA[A/G]TCCCAGCTACTCAGG | 57602 |
rs375371322 | in-del | A/GAGACC | | | intron-variant | USP36 | GRCh38.p7 | 17:78813271 | CACCAGAAAGCAAGA[A/GAGACC]CCTCAAACACCTCAG | 57602 |
rs375394252 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811043 | CGCTTGAACCCAAGA[A/G]GCGGAGGCTGCATAG | 57602 |
rs375431712 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798478 | ACAGACCAGAAGTTC[C/T]GTCGAGTCTGAAGTT | 57602 |
rs375445391 | in-del | -/GT | | | intron-variant | USP36 | GRCh38.p7 | 17:78795030 | AAAAAAAAAAAAAAA[-/GT]AAAAACCACAGCCTC | 57602 |
rs375456800 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822560 | GTCAGACGTGGGCTT[C/T]GGGGTCAGGAGCCCT | 57602 |
rs375485819 | in-del | -/TTTTTTTTTTTT | 0.485731 | 0.0832509 | intron-variant | USP36 | GRCh38.p7 | 17:78791130 | CCCAATCTGGCCTTC[-/TTTTTTTTTTTT]TTTTTTTTTTTAGCT | 57602 |
rs375492511 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818727 | AAGGGTTAAGACGTT[C/G]GATGTTCTGTGGATG | 57602 |
rs375496662 | snp | C/T | 8.24491e-05 | 0.0064201 | intron-variant | USP36 | GRCh38.p7 | 17:78798378 | CCCACCTCACCCTTA[C/T]ACCCACCCCCTCGGA | 57602 |
rs375531154 | snp | A/G | 4.97236e-05 | 0.00498591 | intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806305 | CAGTTATCGACATAA[A/G]TAAAAACTTGGTGGT | 57602 |
rs375588270 | snp | A/G | 0.000142837 | 0.00844973 | intron-variant | USP36 | GRCh38.p7 | 17:78803346 | TTTGCTTTGTTTCTC[A/G]TCAGAGGTAGACAGA | 57602 |
rs375639709 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78808544 | GCCTGAGCAACTGCA[A/C]CCTGCCTGTCGGCCT | 57602 |
rs375730032 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78824976 | AAGACATGACAGTTA[C/T]GAATATCTAACCACA | 57602 |
rs375764090 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837249 | AGTGAGGAAGGAGAA[G/T]AAAAGCAAGTAGCAG | 57602 |
rs375786168 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816380 | CCTATAATCCCAACA[C/T]TTTGGGAGGCCGAGG | 57602 |
rs375796805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802241 | GGTCCCCCAACCCCT[C/T]GCCCGGTGCACACCC | 57602 |
rs375802757 | snp | C/T | 0.000215405 | 0.0103757 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807593 | ATGGGCACACCAATC[C/T]CTTCAGTGGTGTGCG | 57602 |
rs375835435 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806221 | CATGGGGTGGGTGAG[A/G]TCGGAGGATGGTGAG | 57602 |
rs375841163 | snp | C/T | 2.35668e-05 | 0.00343262 | intron-variant | USP36 | GRCh38.p7 | 17:78829058 | GAGCTTTCAAAGAAC[C/T]CACGGTGAGGCCCCC | 57602 |
rs375883238 | snp | A/C | 0.000221828 | 0.0105292 | intron-variant | USP36 | GRCh38.p7 | 17:78835520 | AGGAAGAAAGGGACA[A/C]GGGAAGAAAAGAGGA | 57602 |
rs375908018 | snp | A/C | 0.000153988 | 0.00877328 | stop-gained, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836138 | CCGGTGGGTCATCTC[A/C]ACTCTTGTGGCGACT | 57602 |
rs375924904 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78797992 | ATGGCATCTCGATGC[A/G]GCTGGCAAGAAGTCA | 57602 |
rs375949429 | snp | A/G | 5.42491e-05 | 0.00520784 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821045 | GTCCGAGACGCTCTT[A/G]CACACGGAGCACTTC | 57602 |
rs375972305 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78830958 | CAGGCCAGATGCAGT[C/G]GCTCACGCCTGTAAT | 57602 |
rs376009031 | snp | A/G | 1.6522e-05 | 0.00287414 | intron-variant | USP36 | GRCh38.p7 | 17:78813015 | TTCTGTCAAAGGAAG[A/G]AAACAAGTAGGGAAT | 57602 |
rs376063903 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795786 | ATGCAACCAGGACGC[A/G]GGGCAGGCAAGTGAG | 57602 |
rs376077589 | snp | C/T | 9.03138e-05 | 0.00671928 | intron-variant | USP36 | GRCh38.p7 | 17:78802310 | CGGTTCCCACCCCCT[C/T]GCCCGGTGCATACCC | 57602 |
rs376077925 | snp | A/G | 0.000445078 | 0.0149111 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806224 | GGGGTGGGTGAGGTC[A/G]GAGGATGGTGAGGGG | 57602 |
rs376092519 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78838111 | TAAAACAAAAAAAAT[C/T]GTGGCTCACGCCTGT | 57602 |
rs376112518 | snp | A/G | 1.66161e-05 | 0.00288232 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836377 | ATGGTGCATCACTGT[A/G]GGGACAAGAAGAAAC | 57602 |
rs376188152 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793514 | AAGGCGGGATCTGCA[C/T]GAAGCAGCAGCAGGG | 57602 |
rs376191854 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | USP36 | GRCh38.p7 | 17:78833008 | ACAAAATTAGCCAGG[A/C/T]GTGGTGGCGGGCACC | 57602 |
rs376198256 | snp | A/G | 0.000103943 | 0.00720837 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803850 | ACCTGAGGCAGCGCC[A/G]TCGAGATGGAGGAGC | 57602 |
rs376200057 | snp | C/T | 8.37921e-05 | 0.00647217 | intron-variant | USP36 | GRCh38.p7 | 17:78799802 | AGAAACATTTACAGA[C/T]GTTTAAAATAACCCA | 57602 |
rs376324286 | snp | C/T | 8.29621e-05 | 0.00644004 | intron-variant | USP36 | GRCh38.p7 | 17:78818820 | AATGAATGATTGATT[C/T]GTGCTCTGAAAAATG | 57602 |
rs376348794 | snp | C/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842054 | CCAACACTTGGAGGC[C/G]AAGGTGGGCGGATCA | 57602 |
rs376357967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806102 | CACCAGCCAAGCACA[C/G]GCAACCACAGGGAGA | 57602 |
rs376368436 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820410 | CAACACTACAGTGAG[A/C/G]TATGATTGCGCCACT | 57602 |
rs376411978 | snp | C/T | 2.1095e-05 | 0.00324763 | intron-variant | USP36 | GRCh38.p7 | 17:78835248 | AATCCAGAGGACCCA[C/T]AGCCACCCCACTGCT | 57602 |
rs376419872 | snp | C/T | 6.60262e-05 | 0.00574532 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806266 | GAGGTCATTGCCGGT[C/T]GCCCTCCACAGGGTG | 57602 |
rs376492638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828292 | TAAGTATTTCACAGT[A/G]CTACAATTTACACAG | 57602 |
rs376513018 | snp | A/G | 0.000165153 | 0.00908565 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807140 | GAATCGCAGAGATGG[A/G]CCGCTCCACTCCTGG | 57602 |
rs376574043 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794522 | CCCTGCCCTGGAGCC[A/G]TCAGTCCTGCCGGTG | 57602 |
rs376647129 | in-del | -/ATT | | | intron-variant | USP36 | GRCh38.p7 | 17:78812644 | CAGTGAGCCGAGATT[-/ATT]GGAGATCGCACCACT | 57602 |
rs376693556 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802946 | GAGATATTTTTTCTT[A/T]TTTCTTTTTTTTTAG | 57602 |
rs376699098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78825286 | GAAATATTATCAACA[C/T]GCTCTGATCATAATG | 57602 |
rs376772768 | snp | C/T | 9.89209e-05 | 0.00703212 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807102 | TTTTGGAGTGGCCAG[C/T]GGTGGAACAGTTCGT | 57602 |
rs376839598 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810018 | TGCCCAGCTAACTTT[C/T]GTATTTTTAGTAGAG | 57602 |
rs376840758 | in-del | -/AAGACTTCTCACCAACTGAA | | | intron-variant | USP36 | GRCh38.p7 | 17:78838497 | TCATGAGAATTATCA[-/AAGACTTCTCACCAACTGAA]CAATCACTGCTGCGT | 57602 |
rs376944310 | snp | A/C/T | 0.000131936 | 0.00812116 | intron-variant | USP36 | GRCh38.p7 | 17:78813759 | CTCATCTGGGGAGGG[A/C/T]GTGAGTTTATTACCG | 57602 |
rs376976440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802277 | GTCCCCCAACCCCTC[A/G]CCCGGTGCACACCCA | 57602 |
rs377039808 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | USP36 | GRCh38.p7 | 17:78798557 | TTTTCTTTTCCTAGA[C/G]CAAGAATCACAGGCA | 57602 |
rs377116586 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820101 | GGTCTTTTTTAGGCT[A/G]AGGCAGCAAATCACA | 57602 |
rs377142544 | snp | C/T | 1.66626e-05 | 0.00288635 | intron-variant | USP36 | GRCh38.p7 | 17:78806950 | GCGGCGAGACCCCCA[C/T]ACACCCACCTTCTTG | 57602 |
rs377166812 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836184 | GGGGTTGAGCAACAC[A/G]TATTTGCTCTTTAAG | 57602 |
rs377168449 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798915 | CATCATACCTTCCCT[C/T]GGTCAAACTCTTCGT | 57602 |
rs377223052 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78820370 | TAGTACCAGCTGTGT[G/T]GGAGGATCACTTAAG | 57602 |
rs377253280 | snp | A/T | 0.000156262 | 0.0088378 | intron-variant | USP36 | GRCh38.p7 | 17:78827374 | AGAAACAGGGAGGGA[A/T]GAGCTCGTGTCTTCT | 57602 |
rs377310938 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812724 | AAAAAAAAAAGAAAA[-/G]AAAAGAAATAACATC | 57602 |
rs377312015 | snp | A/G | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807311 | GGTGAGGTAGAGAGG[A/G]CAACATCCCTGCTGT | 57602 |
rs377321015 | snp | C/T | 1.65562e-05 | 0.00287712 | intron-variant | USP36 | GRCh38.p7 | 17:78814406 | GCACTGACACAAGCC[C/T]CTCACCTTCACGTAG | 57602 |
rs377372763 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796989 | ATTTAAATTCCAAAG[C/T]ACTCACAAAATTGAG | 57602 |
rs377398101 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78827887 | GCAATCTCCAGCCTG[C/G]GCAATAGAGCAAGAC | 57602 |
rs377403888 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828825 | GCCTGGGCAACATAG[C/T]GAGAACCCCATCTCT | 57602 |
rs377404560 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78804322 | CAAAATTAGCCGGGC[A/G/T]TGGTGGCACACGCCT | 57602 |
rs377413168 | in-del | -/TAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78800968 | GCCATGTTAGGGCAG[-/TAT]TTTTTTTTTTTTTTT | 57602 |
rs377467563 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, synonymous-codon | USP36 | GRCh38.p7 | 17:78823133 | CACTTCCCAGACTCC[A/G]GGAGCTCTGAAATAC | 57602 |
rs377491688 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838862 | TACCACGAAAAAGCC[A/G]TCCAAGGAGCATCCA | 57602 |
rs377551507 | snp | A/G | 0.000500526 | 0.0158118 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807238 | CCTGTCGAGGCCAGC[A/G]CTCTCGTCGTTCCCC | 57602 |
rs377756455 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant | USP36 | GRCh38.p7 | 17:78819898 | TTTCCCGTCTGGTAT[C/T]AGTCTTCTGCCACAA | 57602 |
rs386799570 | in-del | AACC/GCATGCCCCAGCCAGCCCT | | | intron-variant | USP36 | GRCh38.p7 | 17:78801569 | CGGGTGCCTGCCAAG[AACC/GCATGCCCCAGCCAGCCCT]AAAGAAAACAAAACA | 57602 |
rs386799572 | multinucleotide-polymorphism | ACTG/GTTC | | | intron-variant | USP36 | GRCh38.p7 | 17:78822717 | TACTCACGCTGGAAG[ACTG/GTTC]TGAAACAATACACCA | 57602 |
rs397710638 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842613 | TAAAAAAAAAAAAAA[-/A]GAAAGAAATGCAACG | 57602 |
rs398031703 | in-del | -/TT | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78831962 | TAGGCTGAAAGAAGC[-/TT]TTTTTTTTTTTTTTT | 57602 |
rs398041939 | in-del | -/G | 0.5 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78825747 | CTAAGAGCGCTCCAG[-/G]TGGCTGCACCCTGTG | 57602 |
rs398100642 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78815716 | TTTTCATAGAAAAAA[-/A]TACACGCACACATAT | 57602 |
rs527277418 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825641 | ATCCAAACCGTTATT[C/T]ATTCTACCTCCCATC | 57602 |
rs527508431 | in-del | -/TTTTTTC | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78802937 | TTATCAGAGGAGATA[-/TTTTTTC]TTTTTTCTTTTTTTT | 57602 |
rs527526317 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP36 | GRCh38.p7 | 17:78839839 | CACACTCTACCCAAC[C/T]CAGGAAGGATGCTCT | 57602 |
rs527541476 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840973 | CCGCTTCCGTGTCGC[C/T]TACGTCACCTCCCCA | 57602 |
rs527553574 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827787 | GATGGCATGTGCCTG[C/T]AGTCCCAGCTACTTA | 57602 |
rs527576124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78806432 | GAAGACAAAAAGGGG[A/G]GGTGAGGGGCAGGGG | 57602 |
rs527586723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810455 | ATTAAACCTGGCTAG[A/C]TTTTGCATTTTTAGT | 57602 |
rs527598493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816029 | CATATATTCTTAGCA[A/G]TAATAGTGCCTGGCA | 57602 |
rs527700965 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793086 | TCTGATTCTACTTCC[A/G]TCAGTATCGAATGCC | 57602 |
rs527708930 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841379 | TGCAGTTTGGGGAGG[C/G]AGGGATCTGGGAGCG | 57602 |
rs527841421 | in-del | -/GCCCGCCCCGGGGCCGC | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78840323 | AACCACGAGGAAGGT[-/GCCCGCCCCGGGGCCGC]ACCCGCCCCGCTGAG | 57602 |
rs527876523 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78800426 | GGACAGCACTCACCA[-/C]CCTCATCGGGTTCTA | 57602 |
rs527885068 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78831053 | TACACAGTGAAACCC[C/T]GTCTCTACTACAAAT | 57602 |
rs527886386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78825465 | AGCTCCCTCATGGAC[C/T]GACATCTGGTGAGCC | 57602 |
rs527937362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790818 | TCTGGTCTCATGATG[C/G]TAAGAAGCTACCTAA | 57602 |
rs527967818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816619 | TGACAGAGTAAGACT[C/T]CGTCTCAAAAAAAAA | 57602 |
rs528043575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817021 | ACATGTTTTGGTCAA[C/T]GACAGACCACATATA | 57602 |
rs528058880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811640 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCAGGAGG | 57602 |
rs528125121 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78807723 | CACAGTGAATCTTAG[C/T]AGCAGGCATGGCCTC | 57602 |
rs528182448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812409 | TAAGAAATAACATTG[A/G]CCGGGCGCGGTGGCT | 57602 |
rs528190959 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807489 | GTGTGGGTGTCTGGG[A/C]GAGTTTGGGGGAAGG | 57602 |
rs528255264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837961 | GCAGTGGCCTGGGCC[G/T]GTCGTCCCAGATGCT | 57602 |
rs528273842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831880 | CTTGGGAGGTGGAGG[G/T]TGCAGTCAGCTATGA | 57602 |
rs528308479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837112 | ATATTGAGTTAAATA[A/C]ATTATGAAAATGAAT | 57602 |
rs528331338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802959 | TTTTTTCTTTTTTTT[A/T]AGACAGGGTTTAGCT | 57602 |
rs528336319 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798520 | TTGAAGTTTCTCCTC[C/T]TCTCTCTCTTAAATT | 57602 |
rs528419094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78832255 | AGGAGCTGCTGCTCC[A/G]TGCCACGTGCACAGT | 57602 |
rs528472457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793546 | CACCTCCGGGCAAGA[C/G]TGTGACTCCAGGGAG | 57602 |
rs528513550 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792804 | GCTCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 57602 |
rs528523900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792962 | CTCAAGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 57602 |
rs528538245 | snp | A/C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787111 | CTCCCGAGTAGCTGG[A/C/G]ATTACACGCACGCGC | 57602 |
rs528571342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798639 | TGCAGGTCCTGCACA[C/T]AGGCCGGGCTCTCAT | 57602 |
rs528610659 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795830 | GGTAGCTGCTGTACA[C/T]AGGCCCCACTCCCTC | 57602 |
rs528629083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817883 | CCCAGGAGTTTGAGA[A/C]CACCCTGGGCAACAC | 57602 |
rs528678054 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833715 | GAAAACATCCTGCAT[G/T]CCTAGGATAAACATA | 57602 |
rs528684942 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806547 | ATCACATCCACGTGC[C/T]GTGGCTGCCCAAGCT | 57602 |
rs528779038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808836 | CACCAGCAACTCAAG[G/T]GTCTGGTATAGAGTC | 57602 |
rs528915593 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800056 | TTAATTTACTAATGA[C/G]CTGACACAATAGAGA | 57602 |
rs528943669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794382 | CTTACAGTTAGCCAG[A/C]TGAGTCCTGCTGGCC | 57602 |
rs529004012 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78811871 | GACTCCGTCTCAAAG[-/A]AAAAAAAAAAAAGGA | 57602 |
rs529025139 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78823726 | GGCAGCCTTAGAAGG[A/G]CAGTGAAGGGCAAGA | 57602 |
rs529025638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828600 | TCTGCACCACCACAT[A/G]CAGGGCTGTTAGCAC | 57602 |
rs529028151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78833857 | TTATTATTGTTATCC[A/G]AGTTATAGGAACTTT | 57602 |
rs529070364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823277 | AATACTAGCAAGGAC[A/G]TAATCTCTGCATGGA | 57602 |
rs529131796 | snp | C/T | 0.00115428 | 0.023996 | intron-variant | USP36 | GRCh38.p7 | 17:78819897 | ATTTCCCGTCTGGTA[C/T]CAGTCTTCTGCCACA | 57602 |
rs529135513 | in-del | -/A | 0.49703 | 0.0384237 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842599 | AGCAATACTTGGTCT[-/A]AAAAAAAAAAAAAAG | 57602 |
rs529135568 | snp | A/C | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78794809 | TCAGGAGTTAAGAGA[A/C]CAGCCTGGCCAACAT | 57602 |
rs529152475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78787891 | CAAAAAGAGGGAGAT[G/T]TGGACACAGAACGGA | 57602 |
rs529238960 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78801337 | CTAGCTAGCACCCAC[A/G]TTTTGCTATTTATTT | 57602 |
rs529255484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815458 | TCTTGTCTTTGTCAA[C/G]CATCTCCATTAGTTC | 57602 |
rs529309471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78840391 | CCTCGCCCTGATTCC[A/G]ACTTCAACCTCTCCG | 57602 |
rs529342377 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815904 | AACACATACATGCAC[A/G]CACACATGCATACGC | 57602 |
rs529371029 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837718 | AATATGTCCCTTAAA[C/T]TGCTCACTCACATCA | 57602 |
rs529392706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809864 | GCTGCTTCCTTTTTT[C/T]GAGATGGAGTCCCGC | 57602 |
rs529537712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800756 | CATGCGGCCCCCAGC[A/G]CCTCCTTGCTGAGCA | 57602 |
rs529539723 | snp | A/C/T | 0.000115964 | 0.00761387 | intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806297 | CTGGCCTGCAGTTAT[A/C/T]GACATAAATAAAAAC | 57602 |
rs529629318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78801358 | CTATTTATTTCATAC[C/T]ATTTCATTTTTAACG | 57602 |
rs529644187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790626 | TCTTGGGCTCAAGCA[A/G]TCCTCTCATCTCAGC | 57602 |
rs529688177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78809565 | CACAGGGACTCTCCT[C/T]GAGCCAATCTCCACC | 57602 |
rs529702534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824914 | CAAAAGCCACTCCAC[A/G]TGACAAGTGAAGACA | 57602 |
rs529703755 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797166 | GGGTTATTGCAGCTG[C/G]AAGGGAAGCTACAGC | 57602 |
rs529731792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790069 | CTGTAGCCACATAAG[A/G]CAGAAAAATGGCAGA | 57602 |
rs529742863 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828367 | GTGAATGAGACTTTT[C/T]TATAGCATAGGCAAC | 57602 |
rs529793117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816074 | TGAGTGCACCAGGAC[A/G]GCACAGAGCCCACAT | 57602 |
rs529855474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820709 | GCCGCCCAGAGCACA[A/C]AACAGACTCTCCTCA | 57602 |
rs529864792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811037 | GAGAATCGCTTGAAC[A/C]CAAGAGGCGGAGGCT | 57602 |
rs529881873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816482 | AATACAAAATTTAGC[C/G]AAGCATGGTGGCACA | 57602 |
rs529939411 | snp | A/G | 3.29707e-05 | 0.00406008 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807096 | GCGGCGTTTTGGAGT[A/G]GCCAGCGGTGGAACA | 57602 |
rs529977841 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842235 | CGGAGGTTGCAGCGA[C/G]CTGAGATGTCGCCAC | 57602 |
rs530007212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806842 | AAGACACTTTGTTCC[C/T]CTAACATGAGGGAGG | 57602 |
rs530092595 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP36 | GRCh38.p7 | 17:78831182 | AGTGAGCCAAGATCA[C/T]ACCACTGCACTCCGG | 57602 |
rs530103828 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836839 | GACACACACACACAC[A/C]CCCACGCAATAAATG | 57602 |
rs530147443 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797681 | ACACTGTCGTTTCTC[C/T]TGCAGGGCTGGTCGG | 57602 |
rs530149508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802761 | ATCCTAACTGAGCCA[A/C]GCCTGTTGACGCCAA | 57602 |
rs530169506 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795785 | CATGCAACCAGGACG[C/T]GGGGCAGGCAAGTGA | 57602 |
rs530182409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831712 | TTTTGGGAGGCTGAC[A/G]CAGGAGGATCGCTGA | 57602 |
rs530245291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821254 | TTCACAAAGATGGAT[A/G]TCAATATCTTTGCAC | 57602 |
rs530365540 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78817114 | CACAAATACTTCCCA[C/T]TGTGTTGCAACTGCC | 57602 |
rs530389047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812797 | GCCAACTTCCCAAGT[A/G]TGAGGAGGTCTGTGA | 57602 |
rs530394646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812480 | AGATCCTGAGGTCAG[A/G]AGATCGAAAGCATCC | 57602 |
rs530465766 | snp | C/T | 8.23906e-05 | 0.00641783 | intron-variant | USP36 | GRCh38.p7 | 17:78821924 | AAGCAGTAGAACAAA[C/T]GTCTCCACTTACCGC | 57602 |
rs530606791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832859 | TAGCCATCTCAACAA[C/T]GTGCTTCTGCAGGGC | 57602 |
rs530616110 | snp | A/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803602 | CAGGCTGTCTCTGTG[A/T]CTGCCCCTCCTGCAG | 57602 |
rs530623697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808340 | ACTGCAGCCTCAACC[C/T]TCTGGGCTCAAGAGA | 57602 |
rs530642187 | snp | A/C | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78832357 | CACAGCCAAAGCCCA[A/C]TTAGGGGTCACTCAG | 57602 |
rs530652023 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788349 | TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC | 57602 |
rs530725120 | in-del | -/AGAG | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78832128 | TGACTACACGGACAT[-/AGAG]AGATTTGGGAAACAA | 57602 |
rs530758906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804166 | TAATTCAACATCTAT[G/T]TAAATGCAAAGTTGG | 57602 |
rs530840031 | snp | A/C/T | 3.29652e-05 | 0.00405974 | intron-variant | USP36 | GRCh38.p7 | 17:78798898 | CTGTGGTCAGCATCA[A/C/T]ACATCATACCTTCCC | 57602 |
rs530850322 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787177 | GACGGGGTTTCACCA[C/T]GTTGCCCAGGCTGGT | 57602 |
rs530855724 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791938 | CAGTAGAGATCCTGA[C/T]AGAGGGTGGATCGGT | 57602 |
rs530885210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | USP36 | GRCh38.p7 | 17:78823144 | CTCCGGGAGCTCTGA[A/C]ATACTTGGGGGACCA | 57602 |
rs530911934 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787585 | TGCTGGGAACACACA[C/G]GTCAATGAAGAGCAG | 57602 |
rs530945534 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78828500 | CCACCTGCCCAAAGG[A/C]AAAGCTACCTGTCCT | 57602 |
rs530975961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78808868 | GTGCTTAAAAAATAT[C/T]TGTTGAGCTTTTCCT | 57602 |
rs531004644 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809996 | GGATTACAGGCGCAC[A/G]CCACCATGCCCAGCT | 57602 |
rs531064917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818845 | AAAATGTTGTCTTAA[C/T]GCTAAGTTAATAACA | 57602 |
rs531078042 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833863 | TTGTTATCCGAGTTA[C/T]AGGAACTTTATAGAA | 57602 |
rs531101982 | in-del | -/ATATATATATATATATATT | | | intron-variant | USP36 | GRCh38.p7 | 17:78821404 | TATATATATATATAT[-/ATATATATATATATATATT]TTTTTTTTTTTTTTT | 57602 |
rs531115883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804984 | TACCGTCATTAGGAC[A/G]CTGAAACCGGGACAC | 57602 |
rs531229738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805599 | CAACTTCCTGCCACT[A/C]GAGGCACCTAAGAGA | 57602 |
rs531237606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78800159 | AAAACCCTCCAAAAC[C/T]CCTTTAACCAGTAGT | 57602 |
rs531239856 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78809144 | TTACAAATGTTAACC[-/T]TTTGTTGACAATATT | 57602 |
rs531296047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829137 | AGGCTGTGAGAGAAC[A/G]GCTGAGCCAGAGATC | 57602 |
rs531296296 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840725 | ACCGCCCCGACCCGA[C/T]CCCAGCCTACCCCGG | 57602 |
rs531324299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800669 | GCTCCCAACGTGCTG[C/T]GCCTCCTGCCCTTGG | 57602 |
rs531331752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823877 | AGGCGCTCTGGATAC[G/T]AATCTTGAAAACCAG | 57602 |
rs531335228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833932 | AGAACGTGTAAAGGA[C/T]TGGAATTGTTTCTTA | 57602 |
rs531420782 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824798 | GACAGATCTTAAGAA[C/T]GCCTCTAAGAAAGGG | 57602 |
rs531423516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824315 | GAGAGGAAAAGAGCT[A/G]GGAAGTAAAGGGTAC | 57602 |
rs531478479 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | USP36 | GRCh38.p7 | 17:78815834 | ACATGCACACATATA[C/T]ACATACACACACACA | 57602 |
rs531508350 | snp | C/G | 0.000181727 | 0.00953049 | intron-variant | USP36 | GRCh38.p7 | 17:78820060 | CAGCAGAGGAAAAAG[C/G]CTGATTCAAGAAATG | 57602 |
rs531539138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815630 | TAGCCAACTGCTACC[A/G]CAAGTAAGACTTTTA | 57602 |
rs531545646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820333 | ATTTAAAAAATTAGC[C/T]AGGCGTGGTGGTGCA | 57602 |
rs531562263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810384 | CCTTAATCTCCCTGG[C/T]TCAAGTGATCCTCCC | 57602 |
rs531576284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789145 | GAGGTTGCAGTGAGT[C/T]GAGATTGCGCCATTG | 57602 |
rs531602457 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791211 | GCGATCTCGGCTCAC[C/T]GCAACCTCCACCTCC | 57602 |
rs531702016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806740 | TGAGTCACATGAGCA[C/T]CACCAGATCAGGGCT | 57602 |
rs531728880 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78835134 | CTGCAGCAGGCATGA[C/T]TCAAATTTAGGTTTC | 57602 |
rs531750776 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841331 | AACGTCCCGGGCTCT[A/G]GGGCCATCCGTGACT | 57602 |
rs531770781 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815925 | ATGCATACGCACACA[C/T]ACACACACATATACA | 57602 |
rs531808581 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78813907 | TTGCAGAAAACAAAA[C/T]AATCAACAAGCATCC | 57602 |
rs531824216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801584 | GCATGCCCCAGCCAG[C/G]CCTAAAGAAAACAAA | 57602 |
rs531835369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806390 | ATAAAAACAAAAGAG[C/T]CCAGAAAAAAAGATG | 57602 |
rs531839703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802226 | AGTGCACGCCCATGC[A/G]GTCCCCCAACCCCTC | 57602 |
rs531847906 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842811 | GTTCTAATGTGATCC[A/G]TTTTGGTTACAGCTT | 57602 |
rs531901180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825892 | TTCTCCCAGGAAGCC[A/G]CCTCTGGGTGAGGTA | 57602 |
rs532000370 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792935 | TGGTCAGGCTGGTCT[C/T]GAACTTCTGACCTCA | 57602 |
rs532057767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825352 | ACAAAAAGGCCCCTC[C/T]ACCTGCAAATTAAAT | 57602 |
rs532059466 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797227 | AAAGCAGATGTATTC[A/G]CAGGTATCGAGGGCT | 57602 |
rs532067909 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830481 | ATCCTGCACCTGTCT[C/T]CTTGAGCACATGGGT | 57602 |
rs532244016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811586 | CGTTAAATGTGAGAA[C/T]AGGCCGGGCACAGTG | 57602 |
rs532256474 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78816522 | TCCCAGCTACTTGGG[A/G]GGCTGAGGCAGGAGA | 57602 |
rs532314343 | snp | C/T | 0.0031102 | 0.0393119 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836409 | TAGAGCCATAGATAA[C/T]GAAATCCCGGGACAA | 57602 |
rs532327037 | snp | A/G | 6.60404e-05 | 0.00574594 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807368 | GATCTGCTGCTATTC[A/G]AGTTGCTGGTCCCAG | 57602 |
rs532342831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836930 | AGGCCACAGGCCACA[C/T]GTGGCTACTGAGCAT | 57602 |
rs532383402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812291 | GTGGTGCTGGTCTCA[C/T]GAGTAGAACAGATCT | 57602 |
rs532399316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798187 | ATCCCACACACACCC[C/T]CTTATACACACGCAT | 57602 |
rs532425343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78792936 | GGTCAGGCTGGTCTC[A/G]AACTTCTGACCTCAA | 57602 |
rs532463638 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812516 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57602 |
rs532486020 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820807 | TTTAAATAAAAGGAT[A/G]CGCTTAGGAAAAACT | 57602 |
rs532513803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826837 | ACATATAAATTATAC[C/T]GCAGAGACCTCATTC | 57602 |
rs532664309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813558 | ACATTCAAAACAGCA[C/T]CAATGTGAGGGCAGA | 57602 |
rs532677692 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812876 | TTTCCAGTCAGTGGG[A/G]AGGAAATAATCCCAT | 57602 |
rs532735741 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828702 | AGGGCGAGCACTTAG[C/T]AGGCCTTCAGTAACA | 57602 |
rs532851186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818176 | GCCAGAGCATGCAAC[A/G]GCACCTGTTCTAGAC | 57602 |
rs532906330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804189 | AAAGTTGGCCAGGTA[C/T]AGTGGCTCATGCCTA | 57602 |
rs532927656 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78828539 | CCCACTAAGAGGCTT[C/T]CCCACTGACCCCAGC | 57602 |
rs532965149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828041 | CCAGCCTGGGCAACA[C/T]GGCCAGACCCCATCT | 57602 |
rs532972800 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816005 | CACATATATACATAC[A/G]TGCACACACATATAT | 57602 |
rs533003679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78804757 | TTCTTGTCACCAAGC[A/G]ATTCAAGTATTTTTG | 57602 |
rs533060372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818899 | GAATCTTCATCAATG[A/C]GATTTCGACCTTCTG | 57602 |
rs533144003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794243 | ACTCCACCAGCCGCC[C/T]TTCAGGCCATCAGGC | 57602 |
rs533155832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833277 | TGCATGGCCATCTTG[C/T]GTTCTTTTTTTTATG | 57602 |
rs533206472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793704 | TACCAAGACTTGAGG[A/C]AGGGATTCTCACAGC | 57602 |
rs533232146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78787706 | TCTGAGAAGAGAACC[C/T]TTCCATACTGTTATG | 57602 |
rs533257631 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78818816 | GATTAATGAATGATT[G/T]ATTCGTGCTCTGAAA | 57602 |
rs533318001 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838687 | CTACGCGGAGCTCCT[C/G]AATGTAAGCGCTCCT | 57602 |
rs533399490 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834225 | GTACTCCAGCCTAGG[C/T]AACAGAGTCCGTCTC | 57602 |
rs533409225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788408 | GACCTCGTGATCTGC[C/T]TGCCTCGGCCTCCCA | 57602 |
rs533464534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809454 | GCACCATGTCATTTA[A/G]AGTAAAACGGCTCGT | 57602 |
rs533477210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800241 | ATCCACCTCACCTAC[A/G]GGAGAGGCCCATGCC | 57602 |
rs533478214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814932 | CTCAGCCTGGGCGAC[A/T]GAGCGAGACTGTCTC | 57602 |
rs533550647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78840274 | CAGCAGCATCGGAAC[C/T]GCACCCCGCCCCGGG | 57602 |
rs533567921 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794091 | CCCTATCTGTCATCT[C/T]ACCTCTTGAGTCCAT | 57602 |
rs533579308 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822129 | GGAAACTCCACCCCC[C/G/T]ACCCGAGTCACCACA | 57602 |
rs533590036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78788720 | CATGGGGTAGGTATT[A/G]CTGAGGCCATCAGAA | 57602 |
rs533598016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805691 | GTGTCTGCAGAGGAA[C/T]CCGAGAGCCCTGAGA | 57602 |
rs533632281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800742 | GGACTGCAAGAGCCC[A/G]TGCGGCCCCCAGCGC | 57602 |
rs533661069 | snp | C/T | 0.00120205 | 0.0244863 | intron-variant | USP36 | GRCh38.p7 | 17:78806146 | CAGAAGATCCCGGCC[C/T]AAAGCTTACCTGGCT | 57602 |
rs533663110 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817064 | CATAAGATTATAATA[C/G]TGCATTTTCACTGTA | 57602 |
rs533710040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810134 | CCCCTCTTCTTTTTT[C/T]TGTAGACAAGGTCTC | 57602 |
rs533722897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834528 | GTCAGCTCACTGCAA[C/T]CTCCACCTTCTGGGT | 57602 |
rs533778992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839981 | GGATGAACTGCAACG[A/G]ACGCTCGCAGGGTCA | 57602 |
rs533833865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790678 | AAGCATGAGCCACTG[C/T]GCCCGGCCAACACAT | 57602 |
rs533916134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824557 | TCAAAAAGAATGGTT[A/T]ATGTACAAAGGTAGC | 57602 |
rs533922788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830192 | TATCGTTCTCATTCA[C/T]GTATTATCACACACA | 57602 |
rs533931765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815194 | AAAATTAGCCAGGCG[C/T]GGTGGCACGTGCCTG | 57602 |
rs533960695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835176 | TACATTATGAACTAC[C/T]CTCCTAAATTTGACC | 57602 |
rs533961478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824156 | CACCCAGCCAGGAGC[A/G]CACCAGAGGTGCCAA | 57602 |
rs533974667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801789 | TTCAGGGAGTCATTC[C/T]GTGAGAAGCTGTAGA | 57602 |
rs534045982 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809835 | GGAGATGGGGGTCTT[C/T]CTATGTTGCCCAGGC | 57602 |
rs534049667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834719 | CAGGTGTGAGCCACC[A/G]TGCCCGGCCTTGATT | 57602 |
rs534082774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820827 | TAGGAAAAACTCTAG[A/G]AAAAAACAGGTAAAG | 57602 |
rs534091572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800920 | AAGCCAACTCCACTT[C/T]GCTCCGAGGGTGGCA | 57602 |
rs534141651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820501 | AAAGCAAAGAAATGA[C/T]AGCTGCAGGTCTGCC | 57602 |
rs534205975 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811227 | GAAACTGCTCATGAA[A/T]CCACTTAGTGAAACT | 57602 |
rs534245352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790318 | TTTTTAAAGACAGAG[A/T]CTCACTCTGTCACCC | 57602 |
rs534271811 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808473 | CCCGGCTAGCCTTGA[A/G]TTCCTGAGCTCAAGC | 57602 |
rs534310839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789742 | AAAGACAGCTGGCCA[C/T]GTGCCACGGTTTGGG | 57602 |
rs534313658 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842378 | CGAGGCAGGCAGATC[A/G]CTTGAGGTCAGGAAT | 57602 |
rs534357886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815918 | CGCACACATGCATAC[A/G]CACACATACACACAC | 57602 |
rs534379058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836456 | CTCCTCTTTGGTCAT[C/T]ATGGATGCTAGCCAC | 57602 |
rs534538410 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78831402 | TGGAACACGTGAGGT[C/T]AAGAGTTCAAGACCA | 57602 |
rs534539776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810741 | ATGACCAAAACCCCT[A/G]CAGACTGTGAAAGGC | 57602 |
rs534551829 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797772 | GTGGACACTGGTACC[A/G]GGAGAGCTCCTACCG | 57602 |
rs534571915 | in-del | -/CT | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78830781 | AAGAGATGTAAAAAA[-/CT]CTCCATGAGATTGCC | 57602 |
rs534606266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78835766 | CAGAGACTGAGTGGC[A/G]GAAGGAGCCAGGCCT | 57602 |
rs534636241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791932 | TGTCTACAGTAGAGA[C/T]CCTGACAGAGGGTGG | 57602 |
rs534664024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817383 | CACCACTACCAGTGA[A/G]GAAACGGAGGCTCAG | 57602 |
rs534704803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78802616 | CACCCGCCTGCAACA[C/T]GGAGAAGGTGCCACC | 57602 |
rs534762030 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837212 | ATTACACAGTGCTTG[C/G]AGTACAAATTATCTT | 57602 |
rs534793237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826367 | ACTCTGTCTCTACTA[A/G]TAATACAAAAATTAG | 57602 |
rs534962725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826943 | CCCTAAGAAGGTCTG[C/T]TAACATATTTCCCCC | 57602 |
rs534988399 | snp | A/G | 0.000136638 | 0.00826439 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803728 | GCGTCTCTGAGCCCA[A/G]CCTCTGCGGCTCTCC | 57602 |
rs535073546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822587 | CCCTGCCCTCATTCA[C/T]GTCCCCCGCACCGCT | 57602 |
rs535201902 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78822935 | CTCTCCCCAGGCTCT[A/C]CAGCCCCGTCTCCCC | 57602 |
rs535269618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837621 | CGCTACCTTTGTATC[C/T]ACCACTTGCCCTCCC | 57602 |
rs535301849 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78801186 | TTTCACCGTGTCAGC[A/C]AGGATGGTCTCGATC | 57602 |
rs535357808 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789479 | AGCCTCCTGGACTTG[C/T]TAATTTTGCAGCATA | 57602 |
rs535394443 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814959 | TCTCAAAACTGCCCC[G/T]CCACAAACAAGAAAA | 57602 |
rs535426536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808631 | TTAATTTATATAAGC[C/T]ATATTGTCTCCAACT | 57602 |
rs535455560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832978 | ACATGGTGAAACTTC[A/G]TCTCTACTAAAAATA | 57602 |
rs535455702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839829 | ACACACCATCCACAC[A/T]CTACCCAACTCAGGA | 57602 |
rs535460163 | snp | A/G | 0.000197782 | 0.00994242 | intron-variant | USP36 | GRCh38.p7 | 17:78799039 | CTACCAGGCAGACAC[A/G]GGGGTCAGCACGAGT | 57602 |
rs535505076 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78824138 | TTATGAGAGGCCGGG[A/C]TTCACCCAGCCAGGA | 57602 |
rs535505433 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787264 | TACAGGCGTGAGTCA[C/G]CATGCCCGGCCCTAT | 57602 |
rs535550662 | snp | A/C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808791 | CCAAGAGGCTGTACC[A/C/T]GTTATCTCTCTCGTT | 57602 |
rs535568699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78794557 | TCTGCCCGCCGCCTG[C/T]GAGACGACGTGAGTG | 57602 |
rs535793914 | in-del | -/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796659 | GCTGCCCCAGGGAGA[-/G]GGGGGTGCAGACAGC | 57602 |
rs535812910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78805250 | CGATGTTTGATTACT[C/T]TAAGTGTCTTCTGGA | 57602 |
rs535820351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824451 | TCCAGTTACTGGGCA[C/G]GAGGATTGCTTGAGT | 57602 |
rs535903833 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799382 | GAAGAGCTTCGTCAC[A/T]CTGCCCCTTCCCTAC | 57602 |
rs535943272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800360 | CCTGTCCAGGGGGAA[C/T]CTGGTCCCCATCAGC | 57602 |
rs535946135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810555 | AAAGTGTTGGAATTA[C/T]AGACATGAGTCACAG | 57602 |
rs536008024 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78801046 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC | 57602 |
rs536043610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824096 | CTGGAACTAGAGTGC[C/T]ACACACAGCTGCCCT | 57602 |
rs536068788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829293 | AATGCTGACCTGTGC[A/G]TGATCCTTTTCAGAT | 57602 |
rs536182666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819741 | GTGTAAACTGTAGCT[A/G]TAAAAATCATAGCTA | 57602 |
rs536268593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820148 | AAAAATTTGCCCACT[A/G]GCTGCCAGATTGGGA | 57602 |
rs536272858 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797361 | GTGGCTGGGTGGGGT[C/T]ACCTCTTCCTTTCTG | 57602 |
rs536305424 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840595 | GGGGACGGCCGAAGC[C/T]CTGCGCGGACCCGCG | 57602 |
rs536461171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816302 | GTAGCTGGGACTATA[C/G]GCACGCGCCACCATG | 57602 |
rs536508266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830222 | ATGTGTATCCATGAA[C/G]AATAAATGGCACTGT | 57602 |
rs536625840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831502 | CCTGTAATCCCAGCT[A/C]CTTGGGAGGATGAGG | 57602 |
rs536675468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825093 | CCAAACAGATGAAGG[A/G]GACAAGAGCACATGG | 57602 |
rs536788669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831966 | AAAAAAAAAAAAGCT[G/T]CTTTCAGCCTAATAA | 57602 |
rs536806077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811347 | CCTTTATCATCCTCT[A/C]TCTGTATGTATATGT | 57602 |
rs536808366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821741 | CCACACCCAGCCCTC[A/G]TGGGAATATTCTAAC | 57602 |
rs537012288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802683 | TTCTTCCCCCCACAC[A/G]CATTAGCGGACGCTC | 57602 |
rs537089860 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78821406 | TATATATATATATAT[-/A]TATATATATATATAT | 57602 |
rs537129179 | snp | A/C/G | 0.000515308 | 0.0160439 | missense, stop-gained, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803779 | TCTCAGAGGGGCTCT[A/C/G]GGGGGGCTCACTGGC | 57602 |
rs537136386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798250 | ACACACCACAGACGC[A/G]CCCACACCACACACA | 57602 |
rs537140306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792084 | CAGTGTCAAATCCTG[A/G]GAAGAAGTCGGTGGC | 57602 |
rs537188755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808073 | GATTTGGGAAGAGAA[A/T]AAAGTATAAAGGAAG | 57602 |
rs537236225 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811674 | GCAGATAGAGACCAT[C/T]CTGGCTAATAAAGTG | 57602 |
rs537237324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827546 | GCCACCACTTTCTCA[A/G]TAAGATTGCAGGCTT | 57602 |
rs537273006 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809125 | TTTGAATGAGATCTT[C/T]TGTTTACAAATGTTA | 57602 |
rs537274886 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78838183 | TCAGGAATTCAAGAC[C/G]AGCCTGGCGAAGATG | 57602 |
rs537342050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793833 | GTCCAGACACCTGGG[C/T]TTTTTCCTAACTAGA | 57602 |
rs537352142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799179 | AAGAGGAGGACGGCT[C/T]GACGCCCATGTGTGG | 57602 |
rs537354125 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831499 | TCACCTGTAATCCCA[C/G]CTACTTGGGAGGATG | 57602 |
rs537377560 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78822168 | ACCTCCATCCTCAGC[C/G]CACGCTGCCTGGCAG | 57602 |
rs537384202 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78828233 | AAAAAGAATGTAAAA[C/T]CCATTGAATATCTCT | 57602 |
rs537413951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78807742 | AGGCATGGCCTCTGA[C/T]TAGCATGCTCAAGAT | 57602 |
rs537439978 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792094 | TCCTGGGAAGAAGTC[A/G]GTGGCAAGAGTGGGA | 57602 |
rs537440049 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797659 | GCGGCCACCTCTGCT[A/C]ACACACACACTGTCG | 57602 |
rs537440239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819555 | GTCCCTGGGGCGGCC[A/G]CCCGGTGCCAGCCAG | 57602 |
rs537467049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823023 | ACGTTTCCCACGGCC[A/T]CCCAGACCATTCCAC | 57602 |
rs537473506 | snp | A/C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787435 | GACAATTTCCAAGCT[A/C/G]TAAGTGAAAAAAGCA | 57602 |
rs537474934 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78828258 | ATCTCTCCAAAAGCC[A/T]ATATAAAACACAGGT | 57602 |
rs537476910 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78794458 | GTGCTTCAGGCAGAG[C/T]TCATGACAGGCTCCT | 57602 |
rs537493515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838214 | TTTCTCTACTAAAAA[C/T]ACAAAAAAACTAGCC | 57602 |
rs537530802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819509 | AAAGAAAACACTCCT[G/T]AAGAGGCAAGAGAGC | 57602 |
rs537582547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813715 | GTTAGGGAGGCCCAC[C/T]GGTATAAGAAAAGAG | 57602 |
rs537598653 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819007 | AGATTCTAAAGCAAA[A/C]AAATAAAAGTACTGT | 57602 |
rs537623688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815071 | AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57602 |
rs537653939 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838656 | TAACGGAGGGCTGAG[A/T]TTGGTTGGGCAGGTG | 57602 |
rs537655912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832582 | GCTTACCTGTGCCAG[C/G]TTACGGGGATTTACA | 57602 |
rs537703671 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793828 | CCAGTGTCCAGACAC[C/T]TGGGCTTTTTCCTAA | 57602 |
rs537809230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823376 | TCATCCAGAAGCCCG[A/C]AAGCACCAGCGCCCG | 57602 |
rs537825836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834642 | GAAACCGGGTTTCGC[C/T]ATGTTGGCCAGGCTG | 57602 |
rs537842306 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803468 | CTTCCTGCTGCTCGC[A/G]TGGTGGCCGTCCGTA | 57602 |
rs537848099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828710 | CACTTAGCAGGCCTT[C/T]AGTAACAGATGGAGA | 57602 |
rs537956863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800829 | AGGGCCCAGGGCGCA[C/T]TTCAGTAGACACAAC | 57602 |
rs537962394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78787927 | GGCTACGTGAAGATG[A/G]AAGCACAGTGGAGTG | 57602 |
rs537988095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829680 | TACACACACAGAGAG[C/G]AGGCCAGATGAGTCT | 57602 |
rs538099849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839892 | GCCTCATCCACATTT[C/G]CACCTGCGCGAACCC | 57602 |
rs538276996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800434 | CTCACCACCCTCATC[A/G]GGTTCTAGAAACCCT | 57602 |
rs538310775 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841632 | AACTTCGCTGGCTTC[A/C]TCCCCATTCCCTTGG | 57602 |
rs538334394 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796297 | TGCAAGTCAACACCC[C/T]GAGAAGAAAAGGAAC | 57602 |
rs538362833 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795300 | ACCCCTAAAGAGAAG[C/T]GAAGACATGATGCCC | 57602 |
rs538395223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820193 | ACAAGAAATGAAAGC[A/C]GCCAGGAACAGCGGC | 57602 |
rs538524731 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78815885 | CGCATATACATACAT[G/T]CACAACACATACATG | 57602 |
rs538557138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790149 | GCTGGAGTGCAATAG[C/T]GCGATCTCAGCTCAC | 57602 |
rs538612474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78810618 | TCTGGGCTACAGTGA[C/T]CACCAACTTTGCAAT | 57602 |
rs538615409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821297 | CCCTGCCTGGACTGC[G/T]GACCACCACGTGCGG | 57602 |
rs538620806 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841080 | GGTGACGTCTCCGCA[A/G]CGCACTAGAGGTGCC | 57602 |
rs538681421 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78834808 | ATAAGATATGCTGAT[-/ACA]ACAACAGATGCATAA | 57602 |
rs538738853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806581 | TGCTGCAGAGGTGCC[A/G]GGCACCCCACTGGGG | 57602 |
rs538749164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78811129 | GAGCGAGACTCTGTC[C/T]CAAAAAAAAAAAAAA | 57602 |
rs538822376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78812543 | AAATACAAAAAAAAT[C/T]AGCCGGGCGTGGTTC | 57602 |
rs538918423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837436 | AACCCAGGGACAACT[A/G]CTATGACTTCTCCAA | 57602 |
rs538949913 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78813716 | TTAGGGAGGCCCACC[C/G]GTATAAGAAAAGAGC | 57602 |
rs539027834 | snp | A/G | 0.000142278 | 0.00843319 | intron-variant | USP36 | GRCh38.p7 | 17:78827157 | GGGTAGAAAGGTGCC[A/G]GGCTGGCTGTTGCCA | 57602 |
rs539037667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78826093 | CAGTTCACTGAAGGG[C/T]AGACCTGGGATCATA | 57602 |
rs539094308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798302 | GATACACAGCCCACA[C/T]ACATCATACACACAC | 57602 |
rs539254842 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842704 | AGAGGAATTGAGTCC[A/G]TCTTACCTTGACCTC | 57602 |
rs539269234 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78826222 | GAAAGTTGCCTTCAT[A/G]TAAGTGATTTAAGTA | 57602 |
rs539276256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822492 | GTGGGAACAAAGGCA[C/G]AAACAGGACCAAATC | 57602 |
rs539317842 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78812073 | GCACTGATAGTCCCG[A/C]ATACTAGGGATGCTG | 57602 |
rs539321111 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78830814 | TACATAAAGGGGAGG[-/T]TTTTTTTCATTTTAG | 57602 |
rs539455723 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78828255 | AATATCTCTCCAAAA[-/G]CCAATATAAAACACA | 57602 |
rs539474892 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806793 | TCACCCCAAGATAGC[C/T]GTTCTTTAATTGCAA | 57602 |
rs539505294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833096 | GGGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 57602 |
rs539578086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822885 | GGAGGCTGCGCAGTG[C/T]GCCGGTGCACCCACT | 57602 |
rs539612182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788262 | CTCCGCCTCCCAGGT[C/T]CAAGCAATTCTCCTG | 57602 |
rs539626615 | snp | C/G | 0.00279162 | 0.0372561 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787239 | CCTCAGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 57602 |
rs539632089 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789053 | AATATGAAAATTAGC[C/T]GGGCGTGATGGCATG | 57602 |
rs539645942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814683 | GGGGGCCGGGCACAG[C/T]GGCTCACGCCTGTAA | 57602 |
rs539702038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78795016 | CTGTTCGGGAAAAAA[A/G]AAAAAAAAAAAAAGT | 57602 |
rs539704028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788134 | AGCTCTGCAAGTTGT[A/G]TTTAAAATTGCATAT | 57602 |
rs539726006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813733 | TATAAGAAAAGAGCA[A/G]AGGGAGTGAGCTCAT | 57602 |
rs539750827 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832792 | TTACTGAAAGTCCAC[C/T]CAGAACCACCTCAAA | 57602 |
rs539767372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794533 | AGCCGTCAGTCCTGC[C/T]GGTGGGACTCTGCCC | 57602 |
rs539767751 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78818440 | AACCCAGAAACGTCT[A/G]TTTTTAAAAGGCGTC | 57602 |
rs539790649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813122 | GAAACCCTGCCAGTC[C/T]TAACCACTTCTCTGG | 57602 |
rs539813992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78808600 | TATGTACTACTGATA[C/T]ACATTAACTGTATGG | 57602 |
rs539922086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805214 | TCATCTAAACAAACT[A/G]TAAGGGCCATGCCAG | 57602 |
rs539933650 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78829819 | AATCTTGGCTCACTG[A/C]AACCTCCGCCTGCCG | 57602 |
rs539946919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808990 | GATGCAAAATGCCAA[A/G]CTGCTTTTACTATAC | 57602 |
rs539952484 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790541 | TGTGATCTGTCTGCC[A/G]TGGCCTCCCAAAGAG | 57602 |
rs539963974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838830 | TCCCAGGGATGCGGC[A/G]CGCACCGGGAACCCT | 57602 |
rs540023304 | snp | A/G | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795513 | CTCTCATAACCTCCT[A/G]GTCACTGAGCTCCCT | 57602 |
rs540043892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78833473 | CTTCTATAGCACTCC[C/T]TCTTTGCGGGCTGCT | 57602 |
rs540048371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834279 | AAATAACATTGTCTC[C/T]GCTTGGGGTTTTTTA | 57602 |
rs540111477 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797802 | GTGACAGGCTCCCAG[A/C]GCAGCAGAGCCCACA | 57602 |
rs540139153 | in-del | -/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797478 | GAAGCAAGGGATGGC[-/T]TGCCCAGAGCCACCA | 57602 |
rs540153577 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795445 | CGCTGCACGGCAACC[A/C]GCCTGCGCCCCGGGG | 57602 |
rs540167539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78800460 | ACCCTTTCTGAACTC[A/G]TCCTCTGCCCAGCTA | 57602 |
rs540178544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829253 | AAACTCTCACCATCA[C/T]AACCTCACACCATCA | 57602 |
rs540180388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823391 | CAAGCACCAGCGCCC[A/G]CAGGGCCACAAGGAA | 57602 |
rs540252609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824177 | GAGGTGCCAACTGGA[C/G]GGTGGGCAATGAGCA | 57602 |
rs540293299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839409 | ACTCCCGAAAAATGT[A/G]TAAGGAAATGATCTC | 57602 |
rs540372637 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812714 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 57602 |
rs540454498 | snp | A/G/T | 1.82022e-05 | 0.00301675 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803936 | GTGGGGGCTGAAGGG[A/G/T]GGTTGCAGGCGGCTG | 57602 |
rs540488378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815817 | ACATACATCGTATAC[A/G]CACATGCACACATAT | 57602 |
rs540532519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794740 | CAGCCAGGCGCAGTG[A/G]CTCACGCCTGGAATC | 57602 |
rs540585589 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841178 | GCCCCCGCCCCAGAA[C/T]GGGGACTCGAGGGAC | 57602 |
rs540667441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78788996 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCT | 57602 |
rs540669021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830287 | GTATCATGCAGTTAC[A/G]TATCATTCAGCAATG | 57602 |
rs540713274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790527 | TGAACTCCTGACCTT[C/G]TGATCTGTCTGCCGT | 57602 |
rs540808502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78834160 | GCTGAGACAGGAGAA[C/T]TGCTTGCACCCAGGA | 57602 |
rs540847131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78809812 | ACTTTTTTTGGAGAT[A/G]GGGTTTTGGAGATGG | 57602 |
rs540870091 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815785 | AAATACATGCACACA[C/T]ATATACATACATGCA | 57602 |
rs540871980 | in-del | -/ATATATA | | | intron-variant | USP36 | GRCh38.p7 | 17:78821414 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 57602 |
rs540896315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835040 | AGTATCTTTTGAAAA[C/T]GTTTCTGTCTGGGTA | 57602 |
rs540946144 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830177 | CCTGAATTAGGCAAT[C/T]ATCGTTCTCATTCAT | 57602 |
rs540973583 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78802824 | GATCCTGGCCTGGCC[C/T]GGGACACCTGATCCA | 57602 |
rs540986610 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796662 | TGCCCCAGGGAGAGG[A/G]GGTGCAGACAGCGAG | 57602 |
rs541088044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825205 | CACCGCCAAGCATGC[A/G]GGAAACATTCACAAA | 57602 |
rs541105702 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824051 | AACTCCAAGCCGAAC[A/G]TCCTCAACACAGTGA | 57602 |
rs541169522 | snp | C/T | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807263 | TTCCCCTTCAGCCCA[C/T]GCCCGTTGGCAGTGG | 57602 |
rs541225515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826749 | GTGAATAAGAAACAG[C/T]AGCCAGGCACAGTCA | 57602 |
rs541228300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798055 | TATACACACAACCCA[C/T]ATCCCACACACACCC | 57602 |
rs541229363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820653 | CCAAGGCTGCTCTCC[C/T]AGGTGAGGCCCACAG | 57602 |
rs541249540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78825794 | CTGCTATAGGCTCGC[C/T]GCACTCCCCCTGCAG | 57602 |
rs541291302 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78821546 | AATTCTCCTGACTCA[A/G]CCTCCCAAGTAGCTG | 57602 |
rs541370221 | in-del | -/ATA | | | intron-variant | USP36 | GRCh38.p7 | 17:78821418 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 57602 |
rs541414853 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78817701 | GGAGACAGCGCCACT[A/G]CAATCCAGCCTGGGC | 57602 |
rs541542483 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809826 | TGGGGTTTTGGAGAT[A/G]GGGGTCTTTCTATGT | 57602 |
rs541547261 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842863 | CTTTCATCTTTAATG[C/T]TTCTCTAGTTTTCTC | 57602 |
rs541552050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78818115 | TTAAACAATAAAATA[C/T]CATCGTGTCAAAAGT | 57602 |
rs541585516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78812707 | GTCTCGAAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 57602 |
rs541614782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838298 | AATTGCTTGAACACG[A/G]GAGGCAGAGGTTGGA | 57602 |
rs541670725 | snp | A/G | 0.000598229 | 0.0172846 | intron-variant | USP36 | GRCh38.p7 | 17:78827225 | CAAAGCCCTGGGAGG[A/G]TGGGTGGGGAAGCAC | 57602 |
rs541693776 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838749 | AGAGCGGGCGTCAGA[C/G]CCTGTGGGAGGGACA | 57602 |
rs541709662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832766 | GAAAACAACAGCCAT[C/G]TAGTCAAATCTTACT | 57602 |
rs541825792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793589 | ACAAGACACAGAAAG[A/C]TGCCCGTCTGCATGT | 57602 |
rs541855688 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812376 | TTCTCTATAGCCAAT[A/G]TCAGCTGATGACCAG | 57602 |
rs541975660 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833720 | CATCCTGCATTCCTA[C/G]GATAAACATAAGTTG | 57602 |
rs542048581 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78814181 | GGATGGCACCAGAAG[C/T]GGCTGCCTCTTCCGT | 57602 |
rs542060408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78807848 | AACAGGGACCACAGC[C/T]GTGTACCACCACACC | 57602 |
rs542120041 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78804626 | TGATCCCTGAGATTT[A/T]AAAAAAAAAAAAAAA | 57602 |
rs542122672 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794705 | AAGACGGGCAGATCA[C/T]GAGGTCAAGAGATGG | 57602 |
rs542207085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828407 | ATATTCAGAATGGAA[A/T]TGGTACATTCCTCAT | 57602 |
rs542295439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800544 | TTCTCCCTGCCTCCA[A/G]TTCCTCAGTGAGCTC | 57602 |
rs542311539 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825809 | TGCACTCCCCCTGCA[A/G]GTGCTGGGGACACCG | 57602 |
rs542318854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806893 | TCTCACTCCCTTCAA[A/G]CCACAACCAAGCAAC | 57602 |
rs542352807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78805925 | ACAAAGACAGAACTA[A/G]GACATCAGGACTGCA | 57602 |
rs542355014 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78800154 | AAAAAAAAACCCTCC[A/C]AAACCCCTTTAACCA | 57602 |
rs542444155 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818763 | GCGCTTGCTGGCTGG[A/G]ACCTTCTTCTTGCAT | 57602 |
rs542548803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789825 | AAATGTTTTCACTTA[C/T]GCAGAAAAACAAAGG | 57602 |
rs542573790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815831 | CACACATGCACACAT[A/G]TATACATACACACAC | 57602 |
rs542593484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824610 | TTCCTAATATCCAAA[C/G]AAATTTGAGAAATAA | 57602 |
rs542621867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809343 | TGTTCCCTACATTCT[A/G]TTCTTTGTTAATACT | 57602 |
rs542634837 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78840140 | ACCTCTCCCCGAGCA[C/T]GGCTCCGTGGCGAGC | 57602 |
rs542637362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820243 | ACCTTGGGAGGCCGG[A/G]GCAGGAGGATCATTG | 57602 |
rs542669927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839565 | CTTGAGAACCACTTA[A/G]GGAGGGGATAAACGA | 57602 |
rs542680463 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840820 | CGCGCACCATCCGGG[A/C]CTCCGGCGCCTCACA | 57602 |
rs542698093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834501 | AGGCTGGAGTGCAGC[A/G]GCATGATCTTGGTCA | 57602 |
rs542739508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815950 | TATACACACATGCAT[A/G]CACACACATATACAT | 57602 |
rs542783127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824251 | TACCACCTTACAGGT[A/G]CCAACAAAAAAAATG | 57602 |
rs542806309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806715 | AACTGCTACCTTGCC[C/G]AAACCTCCATGAGTC | 57602 |
rs542819988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829488 | ACTGGTTCTAGTAAA[C/T]ACCTCGCTAGGATAC | 57602 |
rs542864326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835890 | GGGGGACAGCAAGTC[C/G]AAGGACCCACCAAGT | 57602 |
rs542867226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810837 | ACAGTCATCCAGGCC[A/G]GGCACGGTGGCTCAT | 57602 |
rs542957495 | in-del | -/CATA | | | intron-variant | USP36 | GRCh38.p7 | 17:78815799 | ATATATACATACATG[-/CATA]CATACATCGTATACA | 57602 |
rs543155133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810371 | TGACTCACTCCAGCC[C/T]TAATCTCCCTGGCTC | 57602 |
rs543159589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78791295 | ATGCACCACCATGCC[C/T]GGCTGATTTTGTATT | 57602 |
rs543250411 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792777 | AGGCTGGAGTGCAGT[G/T]GCATGATCTTGGCTC | 57602 |
rs543322705 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797187 | AAGCTACAGCACAGT[C/T]GTCTCAGAATAAACA | 57602 |
rs543324882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78817470 | TTATGAGATACAGAC[A/G]TCTACTGGGCACGGT | 57602 |
rs543337655 | snp | C/G | 3.30273e-05 | 0.00406356 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807350 | CCCTGCCTTTGGCTC[C/G]CAGATCTGCTGCTAT | 57602 |
rs543374062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790655 | GCCTCCTGAAGTGCT[A/G]GAATTACAAGCATGA | 57602 |
rs543383174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802766 | AACTGAGCCAAGCCT[A/G]TTGACGCCAATGTGC | 57602 |
rs543517429 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824416 | TGAAACCAGCAGGCA[A/G]CATGGAGCGTGCCTG | 57602 |
rs543517695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798169 | ACCCCCTTATACACA[C/T]GCATCCCACACACAC | 57602 |
rs543563444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811473 | CCCAAAATATGTCCA[C/T]GTGTATTTCCAAAGA | 57602 |
rs543626329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78821365 | CTCCTCCCTGCACGC[A/G]TGCACGGCACTTCCT | 57602 |
rs543651492 | snp | A/G | 8.23839e-05 | 0.00641757 | intron-variant | USP36 | GRCh38.p7 | 17:78821925 | AGCAGTAGAACAAAC[A/G]TCTCCACTTACCGCG | 57602 |
rs543687981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792860 | AGTAGTTGGGATTAC[A/G]GGCACAGGCCAAGCC | 57602 |
rs543707885 | snp | A/G | 3.32779e-05 | 0.00407895 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807191 | GAGTCGCTGCTGGCC[A/G]AGTGCTCTGGGCTGG | 57602 |
rs543741444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817745 | TCTGTCTCAAAAAAA[A/C]AAAAAAGAGAAAAAA | 57602 |
rs543748828 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832876 | TGCTTCTGCAGGGCA[C/T]GGTGGCTCATGCCTG | 57602 |
rs543828196 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78818149 | TTTTCTAAACTCCAT[A/C]TTTCATAAAAAGCCA | 57602 |
rs543830970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831759 | CCAGCCTGGGCAACA[C/T]TGCCTAACCAAATCT | 57602 |
rs543834326 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790002 | GCTCCAGTTCACTCA[C/T]TCAACAAATATTTAC | 57602 |
rs543865166 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798729 | CTATTGACAAAGGGG[A/C/T]GGAAGCTGCGAGGAT | 57602 |
rs543870007 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815553 | CAGGAACATTGTTGG[C/T]GGGAGAAAAGGGAGA | 57602 |
rs543892013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832166 | ACAGGACTGAACTGC[A/G]TTCCTCCTAGACTAT | 57602 |
rs543907105 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812643 | TGCAGTGAGCCGAGA[C/T]TGGAGATCGCACCAC | 57602 |
rs543939386 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78787781 | CCAGTACCTGTGAAT[A/G]GTGACCTTATTTGGA | 57602 |
rs543952470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78813987 | ATTTCCAAACACTAT[C/T]AATAATCAACAGGTA | 57602 |
rs543955632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804177 | CTATTTAAATGCAAA[G/T]TTGGCCAGGTACAGT | 57602 |
rs543980960 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820616 | CCCGCACCCTGTAGC[C/T]GCAGCAGGATGTGCG | 57602 |
rs544130588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822599 | TCATGTCCCCCGCAC[C/T]GCTCACTAACTGGGA | 57602 |
rs544287759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP36 | GRCh38.p7 | 17:78823149 | GGAGCTCTGAAATAC[C/T]TGGGGGACCAATACA | 57602 |
rs544312104 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787658 | AGCACCGCTTGATCA[C/T]CTGTGAGGTAGAGAT | 57602 |
rs544420278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824122 | GCCCTCCTGGAGGAA[C/T]TTATGAGAGGCCGGG | 57602 |
rs544423631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78838812 | GCCTTCTCTTCAGCT[A/G]CTTCCCAGGGATGCG | 57602 |
rs544460991 | in-del | -/G | 0.00716266 | 0.059414 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797695 | CTTGCAGGGCTGGTC[-/G]GGAATGTCACCAAAG | 57602 |
rs544488000 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836189 | TGAGCAACACATATT[C/T]GCTCTTTAAGGCCTC | 57602 |
rs544500620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819814 | CACATAGGTTCCTCA[A/G]GAAATGCGAGCAGCG | 57602 |
rs544526297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799315 | TGTCATGTTTGGTCT[C/T]GAAGTCTGAATAAAA | 57602 |
rs544572837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78823587 | GCCCGAGAGCCACCC[A/G]GAATCACAGCTGCAA | 57602 |
rs544593738 | snp | A/G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827807 | CCAGCTACTTAGGTG[A/G/T]CTGAGGCAGGAGGAT | 57602 |
rs544648956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794620 | TAGTGTTTGGGAAAC[A/G]GCAGTTAAGAATGGA | 57602 |
rs544660933 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837651 | CCTACCCACCACCTC[C/T]CAACTTAACCTTCCC | 57602 |
rs544698394 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796603 | AATTCCATCTACACG[C/T]CAGTAACCACCCAGG | 57602 |
rs544707036 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840651 | CTGCGCCCGCCAGCC[C/T]TTCCCGCGCCCCAGG | 57602 |
rs544711617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788250 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 57602 |
rs544726123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819303 | TAAAGATATTCAGCC[A/G]GCTGTAGTAGTGTGA | 57602 |
rs544772639 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78809433 | TTTCCATACACACTA[C/G]AACTTGCACCATGTC | 57602 |
rs544774515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815281 | AGGTTACAGTGAGCC[A/G]AGATCATACCACTGC | 57602 |
rs544814354 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832721 | TGACAGGCCTGGGAT[A/G]GCAGAGTCTTACTGC | 57602 |
rs544835227 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797058 | ATATTGCTAATGGAA[A/G]CCACAGGACTGGTCA | 57602 |
rs544855486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825145 | TCATCAGTAGACCCA[C/T]CCATGGACAGAGGAG | 57602 |
rs544876731 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78805950 | ACTGCAGAGGCCGAA[C/T]TGCCTTCACCACCCA | 57602 |
rs544922942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790458 | ACGAGGCCCGGCTAA[C/T]TTTTTTTTATTTTTA | 57602 |
rs544923813 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827686 | GGTGGGAGGATCACT[C/T]GAGCCCAGGAGTTCG | 57602 |
rs544958957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800684 | CGCCTCCTGCCCTTG[C/G]GTCTGGTGCCCTGCC | 57602 |
rs544959290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78810971 | CTACAAAAATTAGCC[A/G]GGAGTGCTGGCGGGC | 57602 |
rs544970247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809719 | TCAATGCAGCCTTGT[C/G]TTTAAGTGATCCTCC | 57602 |
rs544997488 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839025 | CAGCTCCAGTCTAAT[C/T]TTATTTCCAAAGAGT | 57602 |
rs545009307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820639 | GATGTGCGACAAAGC[C/T]AAGGCTGCTCTCCCA | 57602 |
rs545051994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834515 | CGGCATGATCTTGGT[C/T]AGCTCACTGCAACCT | 57602 |
rs545081498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829920 | TAATTTTTTGTATTT[C/T]AGTAGAGACAGAGTT | 57602 |
rs545274919 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824884 | CACTGACACTGGCCA[C/T]GGCAGAATTCAGAAC | 57602 |
rs545360578 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790093 | GGCAGAATAATACCT[-/T]TTTTTTTTTTTTTGA | 57602 |
rs545476169 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78821386 | GGCACTTCCTAATGA[A/G]AATATATATATATAT | 57602 |
rs545491683 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841337 | CCGGGCTCTGGGGCC[A/C]TCCGTGACTCCCACA | 57602 |
rs545530094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806748 | ATGAGCATCACCAGA[C/T]CAGGGCTCTCTCAAC | 57602 |
rs545555556 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833311 | TTTTGAGACGGAATC[C/G/T]TGTTCTGTTGCCCAG | 57602 |
rs545559053 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78834712 | CCTCCCACAGGTGTG[A/C]GCCACCGTGCCCGGC | 57602 |
rs545612513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816966 | ACCATTAATTTTGCC[A/T]GTTCTTAAACGTCAC | 57602 |
rs545679285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78797969 | AGTCCAACCTAGGAA[C/T]CCAATGCATGGCATC | 57602 |
rs545695874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802696 | ACGCATTAGCGGACG[C/T]TCCACACGCAGCCAC | 57602 |
rs545717970 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820808 | TTAAATAAAAGGATA[C/T]GCTTAGGAAAAACTC | 57602 |
rs545727883 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797585 | CAGCCTCTGCCAGCA[C/G]AGACCACTGTCTATG | 57602 |
rs545730954 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837973 | GCCTGTCGTCCCAGA[A/T]GCTTGGGAGGCTGAG | 57602 |
rs545749274 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837874 | ATTCAAATTTATCAC[C/G/T]GTGGATCATCTAATT | 57602 |
rs545764041 | snp | A/G | 4.9489e-05 | 0.00497414 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803466 | CGCTTCCTGCTGCTC[A/G]CGTGGTGGCCGTCCG | 57602 |
rs545832928 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835684 | AGTAAACCCAGCCAT[C/T]CCACGGACCTCCTAG | 57602 |
rs545911191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832237 | GACAGTCCAGCCTAC[A/G]GCAGGAGCTGCTGCT | 57602 |
rs545971529 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797503 | CCACCAGCTATGCAC[C/T]GGGAGACCACCTGGG | 57602 |
rs545997903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817564 | GTTCGAGACCAGCCT[A/G]GCCACCATGGCAAAA | 57602 |
rs546022905 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787096 | TTCTCATGTCTCGGC[C/T]TCCCGAGTAGCTGGG | 57602 |
rs546034928 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809786 | CACCACCACACCTGG[C/T]TAATTTTTGCACTTT | 57602 |
rs546110701 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787519 | CATGCTACTCGTTTA[C/T]AGGTGTATATTCAGT | 57602 |
rs546119669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809437 | CATACACACTAGAAC[G/T]TGCACCATGTCATTT | 57602 |
rs546169836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815230 | CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT | 57602 |
rs546173418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832701 | GCTCTACAGTGGAAG[A/G]GCCCTGACAGGCCTG | 57602 |
rs546205356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808450 | AGATGGGGATCTTGC[A/T]ATGTTGCCCCGGCTA | 57602 |
rs546263342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828063 | ACCCCATCTCTACAA[A/T]CAATACAAAAACAGT | 57602 |
rs546293023 | snp | A/G | 1.70536e-05 | 0.00292002 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803715 | TGCTGTGGGAGGCGC[A/G]TCTCTGAGCCCAGCC | 57602 |
rs546352311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833303 | TTATGTTTTTTTGAG[A/G]CGGAATCTTGTTCTG | 57602 |
rs546354767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799493 | GCCACCTTCGTGCCA[C/T]GGCTGAGGGTTTAAA | 57602 |
rs546367743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78823178 | CAGGATCATTCAATT[G/T]TTATTCTGCAAAGTT | 57602 |
rs546429253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822889 | GCTGCGCAGTGCGCC[A/G]GTGCACCCACTCCCT | 57602 |
rs546438024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828316 | TACACAGATTTCAAA[A/T]ACCGGTAATAGGCCT | 57602 |
rs546528603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804218 | TATAATTCCAGCACT[A/T]TGGGAAGCCAAGGTG | 57602 |
rs546624698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838431 | TTCAGAAGCTTATTT[A/T]AAAAAAAGCATTATA | 57602 |
rs546681417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819367 | ACCTGAGTTCAGGAG[C/T]TCGAGACCAGCCTGG | 57602 |
rs546684278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832941 | ATCACCTGAGGTCGA[G/T]AGTTCAAGACCAGCC | 57602 |
rs546693471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793746 | TTAAACTGCCCTTAA[A/G]GTCACTATTACAGTT | 57602 |
rs546708644 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823764 | AAGGGGAAACATCAG[C/G]GTCCTGAAAAAAACT | 57602 |
rs546769313 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834435 | CCACATCCAGCTAAT[C/T]GTTTCGATTTGTTTT | 57602 |
rs546780570 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787251 | AAAGTGCTGGGATTA[A/C]AGGCGTGAGTCACCA | 57602 |
rs546837629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78840316 | CCTCCGCAACCACGA[A/G]GAAGGTGCCCGCCCC | 57602 |
rs546838363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818912 | TGAGATTTCGACCTT[C/T]TGCTCCTCTCAAAAT | 57602 |
rs546953346 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796027 | GACTTCGGTGGAGGG[A/G]AGGGACGTGACTCCA | 57602 |
rs546953917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789271 | TTGCCCAATCACTGT[A/G]TGAGTGATTTGTACG | 57602 |
rs547009652 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP36 | GRCh38.p7 | 17:78799585 | GCCACACTCACAGTG[C/T]ACCAGGATCCATTCC | 57602 |
rs547016731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800753 | GCCCATGCGGCCCCC[A/T]GCGCCTCCTTGCTGA | 57602 |
rs547121560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800321 | AAGCTTGGCTGCTGC[C/T]ATCAGGGGCCCGACC | 57602 |
rs547171012 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806018 | TCTTGGTCAGTGACG[A/C/G]CCCCCTGTACCTCCT | 57602 |
rs547273327 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | USP36 | GRCh38.p7 | 17:78799051 | CACGGGGGTCAGCAC[A/G]AGTGCAGGTTCCCAG | 57602 |
rs547276541 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | USP36 | GRCh38.p7 | 17:78815852 | ATACACACACACATA[C/T]GCATGCATACACATG | 57602 |
rs547311933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78795040 | AAAAAGTAAAAACCA[C/T]AGCCTCGCCCATGTC | 57602 |
rs547314644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806438 | AAAAAGGGGAGGTGA[C/G]GGGCAGGGGAATGGT | 57602 |
rs547342462 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78802287 | CCCTCGCCCGGTGCA[C/T]ACCCATGCGGTTCCC | 57602 |
rs547399646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806820 | GCAAATGGCTGGGAA[C/T]GACTAAAAGACACTT | 57602 |
rs547405766 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78801799 | CATTCCGTGAGAAGC[A/T]GTAGACAGAACAGCT | 57602 |
rs547428543 | snp | A/C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809464 | ATTTAGAGTAAAACG[A/C/G]CTCGTCTGCTTGCAG | 57602 |
rs547434860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815725 | AAAAAAATACACGCA[A/C]ACATATACATAACAT | 57602 |
rs547464728 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822648 | CTGGGGCCTCTTCTC[A/T]CCCGGACCCGGGGCT | 57602 |
rs547586840 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78830619 | ATCTATTATCAAATA[C/G]ATCCATCTCATAACA | 57602 |
rs547614557 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797328 | GGGCCACCCTCTCGA[A/G]TTCCATAAAAGGGAG | 57602 |
rs547634219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835181 | TATGAACTACCCTCC[C/T]AAATTTGACCCAGAC | 57602 |
rs547820527 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842436 | AAACCTGTCTCTACT[A/G]AAAATACAAAAATTA | 57602 |
rs548069811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827016 | CGATCCTACCAAGCC[A/G]CCCCGGACCAGCAGG | 57602 |
rs548110236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831901 | TCAGCTATGATTACA[A/C]CACTGGACTCCAGCC | 57602 |
rs548141870 | in-del | -/CACACCC | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78798124 | CAGATGCCAGGTGTA[-/CACACCC]CACACCCAACACACA | 57602 |
rs548159673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78812417 | AACATTGGCCGGGCG[C/T]GGTGGCTCATGCCTG | 57602 |
rs548169424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78817026 | TTTTGGTCAATGACA[A/G]ACCACATATACAACA | 57602 |
rs548197375 | snp | A/G | 4.96849e-05 | 0.00498397 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807167 | CTGGGGGTCTGGGGG[A/G]CCTTGGTGGAGTCGC | 57602 |
rs548354148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78832293 | CGTCAGAACAAACAC[C/T]CCTTAGGATCCTCAA | 57602 |
rs548414591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827416 | CTGCGGCTGCTTTCC[C/T]GAATGGCCATTCCTG | 57602 |
rs548444793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792967 | GTGATCCGCCCGCCT[C/T]AGCCTCCCAAAGTGC | 57602 |
rs548466062 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78831403 | GGAACACGTGAGGTC[A/C]AGAGTTCAAGACCAG | 57602 |
rs548475369 | in-del | -/AT/CA | | | intron-variant | USP36 | GRCh38.p7 | 17:78815849 | ACATACACACACACA[-/AT/CA]TATGCATGCATACAC | 57602 |
rs548499716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804333 | GGGCGTGGTGGCACA[C/T]GCCTGTAATCTCAGC | 57602 |
rs548523649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799559 | TTCTCAAAGCCGAGC[A/G]ATGCCCGCCCGCCAC | 57602 |
rs548565087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832985 | GAAACTTCGTCTCTA[C/T]TAAAAATACAAAATT | 57602 |
rs548601324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78817993 | AGGAGGCTAAGGCAG[A/G]GGGATCGCTTGAGCT | 57602 |
rs548615446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822134 | CTCCACCCCCCACCC[A/G]AGTCACCACAGACCC | 57602 |
rs548629061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78808837 | ACCAGCAACTCAAGG[A/G]TCTGGTATAGAGTCG | 57602 |
rs548666543 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78818230 | AGTCCCACCGCCCAG[C/G/T]GCTCATCACACTCAT | 57602 |
rs548754989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829068 | AGAACTCACGGTGAG[A/G]CCCCCACCCCAAACG | 57602 |
rs548766247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78819461 | GCAGAAACGGAAAAA[C/T]GTCCAAAACCAGTTA | 57602 |
rs548776512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818988 | AAGACTACAGAAAGT[A/G]GGAAGATTCTAAAGC | 57602 |
rs548806968 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821366 | TCCTCCCTGCACGCG[C/T]GCACGGCACTTCCTA | 57602 |
rs548822416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78827761 | AAAAAATAAAAAAAT[C/T]AGCCAGGCATGATGG | 57602 |
rs548845477 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819288 | ACAAGGACCTAGATA[C/T]AAAGATATTCAGCCG | 57602 |
rs548864508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838875 | CCGTCCAAGGAGCAT[C/T]CACGCGTGCACTCAG | 57602 |
rs548871689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788626 | TGTGTGCTACAGGAA[C/T]AACAGACAGCCCACC | 57602 |
rs548900741 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838595 | GACTCACCTGGGATG[A/T]GCAGACTTGGGCCTG | 57602 |
rs549025383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78833335 | TGCCCAGGCTAAAGT[A/G]CAGTGGTGTGATCTC | 57602 |
rs549042875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78787908 | GGACACAGAACGGAA[A/C]GATGGCTACGTGAAG | 57602 |
rs549069283 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78809964 | CGATTCTCCTACCTC[A/G]GCCTCTCGAATAGCT | 57602 |
rs549071158 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840417 | CTCCGAAGTTGACCT[A/G]AATCCTGCACAGACA | 57602 |
rs549104792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794384 | TACAGTTAGCCAGCT[C/G]AGTCCTGCTGGCCAG | 57602 |
rs549137555 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78840255 | CCACGCCACCCGCCA[A/G]AAGCAGCAGCATCGG | 57602 |
rs549191656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835104 | CACCTGACCGATTCA[C/T]CTTCATGGCCCATTC | 57602 |
rs549300476 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78830100 | ACTGCTGTGATCGCC[A/G]AACTCCCCTCAATCT | 57602 |
rs549358631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805746 | GCAGGCAAGACGTCC[C/T]ACAAAAAACGCTCGG | 57602 |
rs549422190 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842671 | CTTCAGCCATCTTCT[A/C]CAGGCTGTGAAACCA | 57602 |
rs549546066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824470 | GATTGCTTGAGTCCA[C/G]GAGGTGGAGCCTGCC | 57602 |
rs549596089 | snp | A/G | 8.24749e-05 | 0.00642111 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836321 | CAGCCGAGTCCTTGC[A/G]GCCGGGTTTCAGGGC | 57602 |
rs549635754 | in-del | -/CTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78808142 | ATTAACATTCTAGTG[-/CTTT]CTTTTTTCAATCTTT | 57602 |
rs549646709 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797389 | CTGAGGACAGGTAAG[A/G]CCAACAGATGAAGGG | 57602 |
rs549656502 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788622 | ACCCTGTGTGCTACA[-/G]GAACAACAGACAGCC | 57602 |
rs549671797 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806854 | TCCTCTAACATGAGG[A/G/T]AGGCCAAAGCCCCCG | 57602 |
rs549708441 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78802299 | GCACACCCATGCGGT[C/T]CCCACCCCCTCGCCC | 57602 |
rs549739457 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796739 | CTGAAGGAGGTCTAA[A/G]TCCAACACCACGTTG | 57602 |
rs549814845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815952 | TACACACATGCATGC[A/G]CACACATATACATAC | 57602 |
rs549843211 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78803279 | ATTTTAGAAAACCAC[A/G]CAAGCAGACTACGTT | 57602 |
rs549883628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810561 | TTGGAATTACAGACA[G/T]GAGTCACAGTCCCAG | 57602 |
rs549886117 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828371 | ATGAGACTTTTTTAT[A/G]GCATAGGCAACTGAT | 57602 |
rs549924801 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78826050 | TAGCTATGGGGCCCA[A/G]CACACAGGGAACAGC | 57602 |
rs549937103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816094 | AGAGCCCACATGACA[C/G]GATTGCCATTATTCT | 57602 |
rs549958059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817176 | GGTTTGTGGCCTAGG[A/G]GCAATGGGCTATACC | 57602 |
rs549964435 | in-del | -/TTTTTTTTTT | 0.272241 | 0.249009 | intron-variant | USP36 | GRCh38.p7 | 17:78799878 | AAGTGGATGCTTGCC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 57602 |
rs549972225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816681 | AGGGTCTCACTATGT[C/T]GCCCAAGCTGGTCTT | 57602 |
rs549978850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821276 | TCTTTGCACTCACAG[G/T]GCCCTCCCTGCCTGG | 57602 |
rs550011943 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795945 | ACATTTACTTACATA[C/T]GTGTACAAGACCTAG | 57602 |
rs550067651 | snp | A/G | 9.88452e-05 | 0.00702942 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836150 | CTCCACTCTTGTGGC[A/G]ACTAGCTCCCTCTGT | 57602 |
rs550097094 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807110 | TGGCCAGCGGTGGAA[C/T]AGTTCGTTTCCTGAG | 57602 |
rs550184546 | snp | C/T | 4.99813e-05 | 0.00499881 | intron-variant | USP36 | GRCh38.p7 | 17:78812819 | GGTCTGTGAGGAGCA[C/T]CAAGACCAGCCACTT | 57602 |
rs550203120 | snp | C/T | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78826811 | AGCTCCCTGTTTGTA[C/T]ATATACATGTACATA | 57602 |
rs550226560 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78831186 | AGCCAAGATCACACC[A/C]CTGCACTCCGGCCTG | 57602 |
rs550324622 | snp | A/G | 3.36151e-05 | 0.00409957 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807535 | CTTTGGAGGAATGCA[A/G]CCGTTCTGGGACTTC | 57602 |
rs550357868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78821583 | CAGGCATGTGCCACC[A/G]CGCCTGGCTGATTTT | 57602 |
rs550483898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822171 | TCCATCCTCAGCCCA[C/T]GCTGCCTGGCAGTCT | 57602 |
rs550522236 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831637 | AGAAATTAAGCCTCT[A/T]ATCATTATATATAAA | 57602 |
rs550678998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798643 | GGTCCTGCACACAGG[C/T]CGGGCTCTCATGAGC | 57602 |
rs550695979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818879 | ACAACTGCTCTGTAA[C/T]AGTGGAATCTTCATC | 57602 |
rs550729147 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788366 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGATGGT | 57602 |
rs550802384 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810113 | AGCCTCCCAAAGTGC[C/T]CGGCCCCCCTCTTCT | 57602 |
rs550821751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822799 | CTGACTCACTGCTCT[A/G]GAACTGCCTTCCTCA | 57602 |
rs550848097 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787213 | ACTCCTGACCTCAGG[C/T]GATCTACCCACCTCA | 57602 |
rs550886026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833981 | GCTGGGCACAGTGGT[G/T]CACACCTGTAATCCC | 57602 |
rs550911300 | snp | A/C/G/T | 0.000223001 | 0.0105573 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803784 | GAGGGGCTCTGGGGG[A/C/G/T]GCTCACTGGCCTCTG | 57602 |
rs550912511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799569 | CGAGCGATGCCCGCC[C/T]GCCACACTCACAGTG | 57602 |
rs550923080 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819590 | AACTGATGTGAGCTC[A/G]TGCTCTGCCACGTCC | 57602 |
rs550974367 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78816388 | CCCAACACTTTGGGA[A/G]GCCGAGGTGGGTGGA | 57602 |
rs551000105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839694 | GTGGGACAGGTCAAT[C/T]TCTACTTCACCAATT | 57602 |
rs551039039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805631 | GCAGGCAGCCCCTGC[A/G]GACCAGGGCCCACAT | 57602 |
rs551069778 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795937 | GGTTATTGACATTTA[C/G]TTACATACGTGTACA | 57602 |
rs551155918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815640 | CTACCGCAAGTAAGA[C/T]TTTTAATCAACTGGA | 57602 |
rs551199455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798827 | CTTCATGCCACTGCC[A/G]CCACCTCCAACTGCC | 57602 |
rs551246987 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793652 | CCACCACGTCCTTGG[C/T]GTACCCACATCCTCA | 57602 |
rs551265125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828776 | TTGGCAGGCCAAAAC[A/G]GAAGGACTGCTTAAG | 57602 |
rs551287180 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78821777 | CTCCAGTGGCCAGGC[A/G]GGCCAAGAGTCTCAG | 57602 |
rs551292546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78820090 | GCCAAATTTAAGGTC[C/T]TTTTTAGGCTGAGGC | 57602 |
rs551293542 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP36 | GRCh38.p7 | 17:78815837 | TGCACACATATATAC[A/G]TACACACACACATAT | 57602 |
rs551365861 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78830207 | TGTATTATCACACAC[-/AT]GTGTATCCATGAACA | 57602 |
rs551425468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819543 | TGGTTGGGCACAGTC[A/C]CTGGGGCGGCCGCCC | 57602 |
rs551445413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806400 | AAGAGCCCAGAAAAA[A/T]AGATGAGGAGACAGA | 57602 |
rs551554077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825412 | ATTGGTGTCATTCTT[A/G]TTTTTTCTCACTCCA | 57602 |
rs551589927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835144 | CATGATTCAAATTTA[A/G]GTTTCATCAGTTACT | 57602 |
rs551592691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78824982 | TGACAGTTACGAATA[C/T]CTAACCACAACCACC | 57602 |
rs551601457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805768 | AACGCTCGGGACTCC[A/G]AGCTCACTCAAGCCT | 57602 |
rs551631499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801669 | AACAGCAAGCAAACC[A/G]TGCTATGTTCTGAAT | 57602 |
rs551634367 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840457 | GGCGACCCCCATCAC[C/T]GGCCCGGAGCCCGGG | 57602 |
rs551662544 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820696 | CCAAAGGCTGCACGC[C/T]GCCCAGAGCACACAA | 57602 |
rs551754817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820823 | CGCTTAGGAAAAACT[C/G]TAGAAAAAAACAGGT | 57602 |
rs551774493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806103 | ACCAGCCAAGCACAC[A/G]CAACCACAGGGAGAA | 57602 |
rs551797241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78834644 | AACCGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 57602 |
rs551882361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788864 | GTGGGGACGGGAGGG[A/C]CACTGAGGACTGAGA | 57602 |
rs551890508 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796765 | CGTTGTCCATCTCCA[C/T]CTGCGACGACTCCGG | 57602 |
rs551930546 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820454 | GGCCACAGAGCAAGA[A/C]CCTGTCCCTCAAGCC | 57602 |
rs552038490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802605 | GAGCGCACAGACACC[C/T]GCCTGCAACATGGAG | 57602 |
rs552113292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790682 | ATGAGCCACTGCGCC[C/T]GGCCAACACATTCAT | 57602 |
rs552126778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792404 | AGCATCTCCAGTAGA[A/G]GTCCCCACAGAGGAT | 57602 |
rs552143454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816539 | GCTGAGGCAGGAGAA[C/T]CGCTTGAACTTGGGA | 57602 |
rs552156146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821127 | CCAGCTCCCAAGACC[A/G]AGACCCAGCAGGGAG | 57602 |
rs552193197 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78811164 | AAAAAAAGAAACAGT[C/T]ATCAAGAGGGTCCAC | 57602 |
rs552228387 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797718 | CACCAAAGAGGTTCC[A/G]ATCTAGAGAAGCCTC | 57602 |
rs552262357 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78830509 | GGTCAGTTTCTCTAA[A/G]GTACACGCTCAGAAG | 57602 |
rs552267345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78821601 | CCTGGCTGATTTTTG[C/T]ATTTTTAGTGGAGAC | 57602 |
rs552329788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811607 | GGGCACAGTGGCTCA[C/T]GTCTGTAATCCCAGC | 57602 |
rs552345677 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812895 | AAATAATCCCATTGC[C/T]GATGTTCTTCTTGGA | 57602 |
rs552360175 | snp | A/G | 6.60306e-05 | 0.00574551 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807376 | GCTATTCGAGTTGCT[A/G]GTCCCAGGCAGCCCC | 57602 |
rs552433681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798213 | CGCATCCCACACACA[C/T]CCTTCTCCAAGTGAC | 57602 |
rs552461234 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812573 | CGGGCACCTATAATC[C/T]CAGCTACTAGGGAGG | 57602 |
rs552471644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78831806 | AAAAAAAAATTAGCT[A/G]GGCATGGTGCTATGA | 57602 |
rs552481144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78807990 | ATTACAGGTGTGAGC[C/T]ATAGCACCTGGCCTG | 57602 |
rs552510511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831394 | GAGGCGGGTGGAACA[C/T]GTGAGGTCAAGAGTT | 57602 |
rs552574419 | in-del | -/CA | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78798241 | GACTAGGACACACAC[-/CA]CAGACGCGCCCACAC | 57602 |
rs552586586 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78840091 | ACTCCGCAGCGCCTG[A/C]CCCGAGCCCGGCCGC | 57602 |
rs552606753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822105 | AGTCACAAGCTCAGC[A/G]TGAGGCTGGGAAACT | 57602 |
rs552637775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826880 | CCTCTTTTCAAAAAC[A/G]ACATGATTTTTAAGA | 57602 |
rs552663418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821841 | CCAGGTCTGCACAGC[A/G]AAGAAAGAGCCCCAG | 57602 |
rs552705615 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | USP36 | GRCh38.p7 | 17:78793208 | GGTTTCCCCATGTTG[-/T]TTTAATTTTGGGGTG | 57602 |
rs552741241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817783 | GAAACACATCTTCTA[C/T]GAAAATGCCACTATA | 57602 |
rs552868457 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78818447 | AAACGTCTATTTTTA[A/C]AAGGCGTCCCAGGTT | 57602 |
rs552940554 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820484 | CCCTATAAAAAAAAA[C/G]CAAAGCAAAGAAATG | 57602 |
rs552945125 | snp | A/G | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78798341 | CCACCACACCCCTAC[A/G]CACATACACGGCACA | 57602 |
rs552956040 | snp | G/T | 8.25089e-05 | 0.00642243 | intron-variant | USP36 | GRCh38.p7 | 17:78813745 | GCAGAGGGAGTGAGC[G/T]CATCTGGGGAGGGCG | 57602 |
rs552956726 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78792666 | TGAGACCAGGGACCA[G/T]GATGGCAACTCTCAA | 57602 |
rs552988581 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814765 | ATCAGCCTGACCAAT[A/G]TAGCGAAACCCCACT | 57602 |
rs553084264 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805497 | CACCAGTACAGTCCC[C/T]GCAGGCCGCCTCATG | 57602 |
rs553108227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813242 | CAGAATTCCTCCAAG[A/G]TCAGAGTTCAATGCA | 57602 |
rs553142463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793048 | AGGCTTTAAATGCTG[A/G]TGCCTAAGCCTCACC | 57602 |
rs553162981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789102 | CTTGGGAGGCTGAGG[C/G]AGAAGAATCACTTGA | 57602 |
rs553172008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818094 | TGTCTTAAAACAAAA[C/T]GAAATTTAAACAATA | 57602 |
rs553177099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833477 | TATAGCACTCCCTCT[A/T]TGCGGGCTGCTACTC | 57602 |
rs553213750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78838961 | TGAACACCTTAACCT[C/T]GACCCCAGACAAGCC | 57602 |
rs553265646 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812154 | ATTGTGCCACTGTAC[C/T]CCAGTCTGGGTAACA | 57602 |
rs553292695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788135 | GCTCTGCAAGTTGTG[C/T]TTAAAATTGCATATG | 57602 |
rs553298106 | in-del | -/TTTA | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786968 | ATACCATGGTTTTAT[-/TTTA]TTTATTTATTTATTT | 57602 |
rs553303799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799601 | ACCAGGATCCATTCC[A/G]CACCCTTCCCTCCTA | 57602 |
rs553395807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804593 | ATCCTGCACATGTAC[C/T]CTGGAACTTAAAATA | 57602 |
rs553403744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808609 | CTGATACACATTAAC[C/T]GTATGGTTAATTTAT | 57602 |
rs553465367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815201 | GCCAGGCGTGGTGGC[A/T]CGTGCCTGTAGTTCC | 57602 |
rs553467064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828325 | TTCAAAAACCGGTAA[C/T]AGGCCTCTTCTTTCT | 57602 |
rs553539999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78806143 | ACCCAGAAGATCCCG[A/G]CCCAAAGCTTACCTG | 57602 |
rs553547917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78793927 | GGTAAGATGCCAACA[C/T]GTCCACTAAGTCAGA | 57602 |
rs553676741 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78823986 | AAACACCTCATGGGA[G/T]GCAAACTAGCTCCAG | 57602 |
rs553736839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78820231 | TATAATCCCAGCACC[C/T]TGGGAGGCCGGGGCA | 57602 |
rs553738831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825038 | GCAAGGAGACAGGCA[C/T]CCACCAGAATTCCAG | 57602 |
rs553746545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829811 | AGTGGCACAATCTTG[A/G]CTCACTGCAACCTCC | 57602 |
rs553775778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824567 | TGGTTTATGTACAAA[A/G]GTAGCCATTAAAACA | 57602 |
rs553785454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834851 | CTAGGCATGGTGGCT[C/T]ACACTTATAATCCCA | 57602 |
rs553811949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78800926 | ACTCCACTTCGCTCC[A/G]AGGGTGGCACGGAGC | 57602 |
rs553824696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820592 | GGCCCAGCAAAGGCA[C/G]ACCACCCTCCCGCAC | 57602 |
rs553878982 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78840094 | CCGCAGCGCCTGCCC[A/C]GAGCCCGGCCGCGGA | 57602 |
rs553897415 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796327 | CATACCCTGCCCGTG[A/T]AGGCATGTGCTTTCC | 57602 |
rs553924838 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78800487 | GCTAGCCACATAGCC[C/G]CTGGAATATACTCAC | 57602 |
rs553971379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834321 | TTAACCAATGCTTTA[A/G]TTTCTTTAATAGTTA | 57602 |
rs554018698 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841878 | CTGGAGATGGGGAGA[A/G]AGGCTAGATGTACTT | 57602 |
rs554048781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840507 | GGACAGCCCGGCCCC[A/G]GACCCTCCTCGGGAA | 57602 |
rs554061576 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841134 | CACCTGGCGGCGTGG[C/T]GGACGCCTGAAGTGT | 57602 |
rs554068057 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78804543 | GGTTGATAGGTGCAG[C/T]AAACCACCATGGCAC | 57602 |
rs554070907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810744 | ACCAAAACCCCTGCA[C/G]ACTGTGAAAGGCCCT | 57602 |
rs554090654 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796909 | TTTCCTGTATTTATT[A/C]AGTTACAAGTTGGCA | 57602 |
rs554164073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830198 | TCTCATTCATGTATT[A/G]TCACACACATGTGTA | 57602 |
rs554182220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835818 | CCCACATGCAGCCCA[C/T]CCCATTTCTCTTTCT | 57602 |
rs554194809 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78809949 | CCTCCCGGGTTCAAG[A/C]GATTCTCCTACCTCG | 57602 |
rs554243564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836523 | AGCTGCACAAAGGAA[A/C]CAGGGAGACCCAGCA | 57602 |
rs554272690 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78800275 | GACCAGCCTGACACC[-/T]TGGATGGCCACAGGG | 57602 |
rs554282909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790320 | TTTAAAGACAGAGTC[G/T]CACTCTGTCACCCAG | 57602 |
rs554298813 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817206 | CATACAGCTGGCTCC[G/T]TCATCTACGTCTGTG | 57602 |
rs554332877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825804 | CTCGCTGCACTCCCC[A/C]TGCAGGTGCTGGGGA | 57602 |
rs554369540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830833 | TTTTCATTTTAGACT[C/T]CTGCTTGCCTTTTCT | 57602 |
rs554411299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811340 | CACATAACCTTTATC[A/T]TCCTCTCTCTGTATG | 57602 |
rs554485864 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78791227 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 57602 |
rs554608025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806937 | CTGATACACAGCAGC[A/G]GCGAGACCCCCACAC | 57602 |
rs554613955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831470 | ATACAAACATTAGCC[A/G]TGTGTGGTGGCAGTC | 57602 |
rs554777075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826381 | AATAATACAAAAATT[A/T]GCCAGGCACGGTGGT | 57602 |
rs554899818 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832657 | ACTGGCTCAAAAAGA[C/T]CCTGCAGAGAAACCA | 57602 |
rs554906426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832150 | TTTGGGAAACAAAAG[A/G]ACAGGACTGAACTGC | 57602 |
rs554926172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78818121 | AATAAAATACCATCG[C/T]GTCAAAAGTAGTTTT | 57602 |
rs554946075 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78812607 | AGGCAGGAGAATGGC[A/G]GGAACCCGGGAGGCA | 57602 |
rs554948916 | in-del | -/G | 0.00438507 | 0.0466187 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836548 | CAGCACTAATCACTT[-/G]GGACATATTAGTTCA | 57602 |
rs554958528 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78824319 | GGAAAAGAGCTAGGA[A/G]GTAAAGGGTACCACG | 57602 |
rs554990532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822591 | GCCCTCATTCATGTC[C/G]CCCGCACCGCTCACT | 57602 |
rs555004147 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790029 | TTACCGGGTGGCTGG[C/T]AAGTGCTAGGCCTTG | 57602 |
rs555017590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818553 | AACCTTTAGAACAGG[A/G]ACAGGTACTGTGTAA | 57602 |
rs555043311 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78824346 | CACGGTGGACTGCCA[A/C]ATCAGACAGTGAGGA | 57602 |
rs555059729 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791366 | CAGGTGATCCGCCCC[A/G]CCTAGGCCTCCCAAA | 57602 |
rs555081017 | snp | C/T | 1.88039e-05 | 0.0030662 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807631 | CATCGTCCCAGAGTC[C/T]TGTCGCTAAGGAGAC | 57602 |
rs555209838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827651 | CTCACACCTGTCACT[A/C]TAACACTTCAGGAGG | 57602 |
rs555215162 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787314 | TTCAGGAACCACCTC[A/G]AAGTTTATCAATAGC | 57602 |
rs555226135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793095 | ACTTCCGTCAGTATC[A/G]AATGCCTCTCCCCAG | 57602 |
rs555353659 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791905 | CCTATACTGAGGGGG[C/G]ACCTCTTTCAGTGTC | 57602 |
rs555382807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833576 | TCCATAGACCAGGGA[C/T]ATTCTCAAAAACTCA | 57602 |
rs555395664 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP36 | GRCh38.p7 | 17:78806401 | AGAGCCCAGAAAAAA[A/C]GATGAGGAGACAGAA | 57602 |
rs555410980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809142 | GTTTACAAATGTTAA[A/C]CTTTTGTTGACAATA | 57602 |
rs555538154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78808671 | AAAAATACTGTACAG[C/T]ATATGTGTGTGTATC | 57602 |
rs555548664 | snp | A/C | 0.000131807 | 0.00811701 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813813 | GCTGGTTCAGAACCA[A/C]CTTGACGTTGCTGGA | 57602 |
rs555609443 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78835885 | GGATAGGGGGACAGC[A/C]AGTCCAAGGACCCAC | 57602 |
rs555712860 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824098 | GGAACTAGAGTGCCA[A/C/T]ACACAGCTGCCCTCC | 57602 |
rs555730553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804677 | ACACGTGATTTTAAA[A/C]GTCAAAAAAAAAATT | 57602 |
rs555736179 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78830241 | AAATGGCACTGTAGC[C/T]ACATGTTTCCAAACT | 57602 |
rs555755023 | snp | A/C/G/T | 0.0013193 | 0.0256504 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799676 | CAGTACCTTTTCTCC[A/C/G/T]GTAAGCTTTATCAGA | 57602 |
rs555798263 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78823530 | GGGGACAAAGGGCAG[G/T]AGAGAACAGCTGGGC | 57602 |
rs555818206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805260 | TTACTCTAAGTGTCT[C/T]CTGGAATCTTTTCCA | 57602 |
rs555876467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78794566 | CGCCTGCGAGACGAC[A/G]TGAGTGTGTTCACTT | 57602 |
rs555880292 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78810179 | CCTGGAATTCACCAG[C/T]GTGATCATGGCTCAC | 57602 |
rs555897351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78802014 | TCTCCCAGACCCTCC[C/T]AAGCTCAGATGCAGT | 57602 |
rs555924430 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829393 | TCGAATTTCTAAGCT[A/G]CATCACATGGTAAAT | 57602 |
rs555964784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801062 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 57602 |
rs556016934 | snp | C/T | 9.88631e-05 | 0.00703006 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806187 | GCCAAGTGGAGGCAA[C/T]GACGGGGTGAGAGGT | 57602 |
rs556067499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815249 | AGGCAGGAGAATCGC[C/T]TGAAACCAGGAGGTG | 57602 |
rs556132349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809702 | AGTGGCACAATGATA[A/G]CTCAATGCAGCCTTG | 57602 |
rs556152074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78825106 | GGGGACAAGAGCACA[C/T]GGATATAGAAAATGA | 57602 |
rs556202106 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841069 | TGCCGCGGCAGGGTG[A/T]CGTCTCCGCAGCGCA | 57602 |
rs556202700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815794 | CACACATATATACAT[A/G]CATGCATACATACAT | 57602 |
rs556277455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834925 | GTTCAAGACTACAAC[A/G]AGTTGTGATGGAGCC | 57602 |
rs556348423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811356 | TCCTCTCTCTGTATG[C/T]ATATGTACGTGTGTA | 57602 |
rs556365997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829887 | CTGGGACTACAGGCT[C/T]GTGCCACCATGCCAG | 57602 |
rs556439170 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841968 | CAAGATAACCATATT[A/T]GTCTGATGCTGAGAC | 57602 |
rs556503138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820881 | GCAGGGAGCAAAGGA[A/G]TTTTCTCCCTATCTA | 57602 |
rs556645511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832021 | AACAATCTAAGCCAG[C/G]TTCTCCAGCAATATA | 57602 |
rs556737074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821371 | CCTGCACGCGTGCAC[A/G]GCACTTCCTAATGAG | 57602 |
rs556836346 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842653 | CACGAAATTAGCCCA[A/G]ATCTTCAGCCATCTT | 57602 |
rs556848402 | snp | C/T | 0.000150006 | 0.00865914 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807220 | GGAGCTGCTGGAGCC[C/T]CTCCTGTCGAGGCCA | 57602 |
rs556940361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802685 | CTTCCCCCCACACGC[A/G]TTAGCGGACGCTCCA | 57602 |
rs556957449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78797917 | CCTGACAGAGAGAAA[A/C]GAGACCCGAATCTTC | 57602 |
rs556963896 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838380 | TGGTCTCAAAAAAAA[A/C]AAAAAACAAAAAACA | 57602 |
rs556997530 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841620 | TTGATCTGAGGCAAC[C/T]TCGCTGGCTTCCTCC | 57602 |
rs557070612 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78827473 | CTTTTCAAAGGAACA[A/C]GTGAGGAAAACAAGA | 57602 |
rs557079176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78792600 | CGGGGGAAGGAGCCC[A/G]GCAACTGGTGTTTTA | 57602 |
rs557140844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792093 | ATCCTGGGAAGAAGT[C/T]GGTGGCAAGAGTGGG | 57602 |
rs557142593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798259 | AGACGCGCCCACACC[A/G]CACACACCACCCAAC | 57602 |
rs557155105 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811782 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 57602 |
rs557246256 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806635 | CCCCTGCTAGGGACA[C/T]GTGCTGGTGGGGCCC | 57602 |
rs557264836 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78807894 | TTTTTGACAGAGATG[A/G]GGTTTCACCATGTTG | 57602 |
rs557279021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793854 | CCTAACTAGAAGACT[C/T]GGAGTTCACCCACTG | 57602 |
rs557292179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809256 | ATTTTATCCTTCAAC[C/T]TTAAGCATACAAAGT | 57602 |
rs557309725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814041 | TATTTTCATAACTCG[C/G]AATGTGACCCCAAAG | 57602 |
rs557321020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808078 | GGGAAGAGAAAAAAG[C/T]ATAAAGGAAGAAATT | 57602 |
rs557398231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814658 | CAGCTTGTCTGGTCT[G/T]TAACAATTTGGGGGC | 57602 |
rs557619342 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787489 | AGAACCATTTGTAAT[C/T]AAAATCAATGTATAC | 57602 |
rs557634432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833043 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 57602 |
rs557665316 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797668 | TCTGCTCACACACAC[A/T]CTGTCGTTTCTCTTG | 57602 |
rs557787020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78839900 | CACATTTCCACCTGC[A/G]CGAACCCCAGCCAGC | 57602 |
rs557889403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78800436 | CACCACCCTCATCGG[A/G]TTCTAGAAACCCTTT | 57602 |
rs557896896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839306 | CCTCAGTAACTACAT[C/T]TGACCCATCCTGAGT | 57602 |
rs557922715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790041 | TGGTAAGTGCTAGGC[C/G]TTGCCAAGAGAACTG | 57602 |
rs557923646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805331 | TTAAGGCCCTCCCAC[A/G]TACACAAATCTTATG | 57602 |
rs557941608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78824538 | GACAGAGCAAGGCCC[C/T]GTCTCAAAAAGAATG | 57602 |
rs558007542 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813820 | CAGAACCACCTTGAC[A/G]TTGCTGGAATGGACC | 57602 |
rs558110172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820194 | CAAGAAATGAAAGCA[G/T]CCAGGAACAGCGGCT | 57602 |
rs558145653 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795375 | TTGCTAAAGGGAGAT[G/T]CGGGGAGCCACACAC | 57602 |
rs558186065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819835 | GCGAGCAGCGGTCAC[C/T]GCTAAGGAAGAGTGG | 57602 |
rs558228681 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841113 | TACTTCCGGGTCGGC[C/T]GAGCACACCTGGCGG | 57602 |
rs558241301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824155 | TCACCCAGCCAGGAG[C/T]GCACCAGAGGTGCCA | 57602 |
rs558259410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806595 | CGGGCACCCCACTGG[A/G]GCTCTGCGCTTCCTG | 57602 |
rs558331313 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, splice-donor-variant | USP36 | GRCh38.p7 | 17:78796316 | AAGAAAAGGAACATA[C/T]CCTGCCCGTGAAGGC | 57602 |
rs558362086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815797 | ACATATATACATACA[C/T]GCATACATACATCGT | 57602 |
rs558381050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78833156 | CCATCTCCAAAAAAC[A/G]CCCCCAAACAATGTG | 57602 |
rs558395821 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78802089 | GGTGCACACCCACGC[A/G]GTCCCCCACCCCCTT | 57602 |
rs558399158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815890 | ATACATACATGCACA[A/G]CACATACATGCACGC | 57602 |
rs558415757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78791863 | GCTTTGGGAGGCCAA[A/G]GCGAGAAGATTATTT | 57602 |
rs558425932 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840681 | GCCTCGCGGAACCCC[C/T]CGCCCCGGTCTCGTC | 57602 |
rs558434593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830019 | GCTGGGATTACAGGC[A/G]TGAGCCATCGAGCCC | 57602 |
rs558461981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791024 | CAGCTGACAATCATG[A/G]TAATTTGAATCTAAC | 57602 |
rs558593971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811902 | TATTTTTTCCTACAC[A/G]CTTACGGTTAAGAGT | 57602 |
rs558606808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835688 | AACCCAGCCATCCCA[C/T]GGACCTCCTAGGCTG | 57602 |
rs558671052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830269 | ACTTCCTTTCTATAA[A/G]TCGTATCATGCAGTT | 57602 |
rs558721260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816347 | AAAAATTTTTTAGGC[C/G]GGGCATGATGGCTCA | 57602 |
rs558732144 | snp | C/T | 0.000100083 | 0.00707331 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807243 | CGAGGCCAGCGCTCT[C/T]GTCGTTCCCCTTCAG | 57602 |
rs558820949 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814024 | TCTATTAAAACGTGT[A/G]ATATTTTCATAACTC | 57602 |
rs558838530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78830731 | GCTTAGCAAATAGAC[A/G]TTAAAATGCTATTAT | 57602 |
rs558838565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825149 | CAGTAGACCCATCCA[C/T]GGACAGAGGAGCAAA | 57602 |
rs558854563 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834725 | TGAGCCACCGTGCCC[A/G]GCCTTGATTTGTTTT | 57602 |
rs558890441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816774 | GAGCCATTGTGCCCA[C/G]CCTAAATCATTTTTT | 57602 |
rs558951478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821306 | GACTGCTGACCACCA[C/T]GTGCGGTACTCTCCT | 57602 |
rs559021691 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823895 | TCTTGAAAACCAGCC[A/G]ACCCACAAGATAAAT | 57602 |
rs559091103 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842744 | GAGCGGACCAGGTAA[G/T]TTTTGGGTGACAATA | 57602 |
rs559135638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817593 | AACCCCATCTCTACT[A/G]AAAATACAAAAATTA | 57602 |
rs559155927 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800869 | GCATGGACCCTGGCG[C/T]ACCGCAAGTGCTCAA | 57602 |
rs559190722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832077 | ACAAATATTTATTCA[C/T]GTAATTTAGGAAAAT | 57602 |
rs559193013 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826345 | CCAGCCTGGCCAACA[C/T]GGCAAAACTCTGTCT | 57602 |
rs559225936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837525 | GCTTGCTACATACTA[C/T]AGTCCCTAACAGAGG | 57602 |
rs559234044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837050 | GAATGTAAAACATCC[C/T]AGTAATTTTTAGATC | 57602 |
rs559250612 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835629 | GGCACCAGAGAAGAA[C/T]TGGTGTTCTGGTTTA | 57602 |
rs559292351 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797876 | ACGCCTTGTCTCCAG[C/G]AGGCTGCAGAACAAA | 57602 |
rs559312189 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78792958 | TGACCTCAAGTGATC[C/T]GCCCGCCTCAGCCTC | 57602 |
rs559325393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821451 | TTTTTTTTTTGAGAT[A/G]GAGTCTTGCTCTGTC | 57602 |
rs559364522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838275 | CTACGCAGGAGGCTG[A/G]GGCAGAGAATTGCTT | 57602 |
rs559391852 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78807680 | TGAGGAAGCGAGAAG[C/T]CTCAGCTGGGCCACA | 57602 |
rs559405371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792158 | TAGACTAAGAACCAC[A/T]GAGAGTCAACACAGA | 57602 |
rs559430495 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78833703 | ATTTTCTGCGATGAA[A/C]ACATCCTGCATTCCT | 57602 |
rs559537536 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787101 | ATGTCTCGGCCTCCC[A/G]AGTAGCTGGGATTAC | 57602 |
rs559565382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78807794 | GGTAAAGACACTGTG[G/T]CTTCTCTGAACAATT | 57602 |
rs559576582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78832238 | ACAGTCCAGCCTACG[A/G]CAGGAGCTGCTGCTC | 57602 |
rs559611462 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837877 | CAAATTTATCACTGT[G/T]GATCATCTAATTCTA | 57602 |
rs559619217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793538 | AGCAGGGCCACCTCC[A/G]GGCAAGAGTGTGACT | 57602 |
rs559677548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818648 | CGGAGCTGCCTGGGA[G/T]GGTGTCACGAGCGCT | 57602 |
rs559697365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804861 | AGGAAAAAAAAGATC[A/C]CGTGAGGATTTATTT | 57602 |
rs559790137 | snp | C/T | 7.38894e-05 | 0.00607776 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803946 | AAGGGGGGTTGCAGG[C/T]GGCTGGATGATTGGG | 57602 |
rs559826409 | in-del | -/AC | 0.00280842 | 0.0373674 | intron-variant | USP36 | GRCh38.p7 | 17:78815928 | CATACGCACACATAC[-/AC]ACACATATACACACA | 57602 |
rs559887509 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78827803 | AGTCCCAGCTACTTA[G/T]GTGGCTGAGGCAGGA | 57602 |
rs559909893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822119 | CGTGAGGCTGGGAAA[C/T]TCCACCCCCCACCCG | 57602 |
rs559946890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818212 | AAGGACATGGACAAT[C/G]CAAGTCCCACCGCCC | 57602 |
rs559976378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819387 | GACCAGCCTGGCCAA[C/G]AAGGTGAAACCCTGT | 57602 |
rs560081715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794799 | GATCACAAGGTCAGG[A/C]GTTAAGAGACCAGCC | 57602 |
rs560159605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78799505 | CCACGGCTGAGGGTT[C/T]AAAGAGGACTCCAGC | 57602 |
rs560268522 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790912 | GATATTTGGCAGCCA[C/T]GTCCTGTTGCTTCCT | 57602 |
rs560268535 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840789 | CCTGGCGACTCCTTC[C/G]GCCCGCGGCCCAGCA | 57602 |
rs560361252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78839661 | GTAGATGCAGAGATT[C/T]TGAACACAATTTTTC | 57602 |
rs560507814 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841385 | TTGGGGAGGGAGGGA[C/T]CTGGGAGCGATCGGC | 57602 |
rs560523175 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78828072 | CTACAAACAATACAA[A/C]AACAGTCAAGTGTGG | 57602 |
rs560603100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830021 | TGGGATTACAGGCGT[A/G]AGCCATCGAGCCCAG | 57602 |
rs560608567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815821 | ACATCGTATACACAC[A/G]TGCACACATATATAC | 57602 |
rs560615307 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802931 | TGGTATTTATCAGAG[A/G]AGATATTTTTTCTTT | 57602 |
rs560615631 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78815790 | CATGCACACATATAT[-/AC]ATACATGCATACATA | 57602 |
rs560678986 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78790056 | CTTGCCAAGAGAACT[G/T]TAGCCACATAAGACA | 57602 |
rs560742337 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796687 | AGCGAGGCAGCCACC[C/T]GGGACAGCAGGATGC | 57602 |
rs560840283 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78827889 | AATCTCCAGCCTGGG[A/C]AATAGAGCAAGACTC | 57602 |
rs560865623 | in-del | -/GTGA | | | intron-variant | USP36 | GRCh38.p7 | 17:78794566 | CGCCTGCGAGACGAC[-/GTGA]GTGTGTTCACTTTTA | 57602 |
rs560889295 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78802178 | CCCCACCCCCTCGCC[C/T]GGTGCACACCCACGC | 57602 |
rs560898297 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797151 | TCAGTGAAGACCTGC[A/G]GGTTATTGCAGCTGC | 57602 |
rs560905972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824908 | TCAGAACAAAAGCCA[C/T]TCCACGTGACAAGTG | 57602 |
rs560913213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811029 | AGAGGCAGGAGAATC[A/G]CTTGAACCCAAGAGG | 57602 |
rs560941661 | snp | A/G | 3.76237e-05 | 0.0043371 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802440 | TGCCCATCCTCTTCT[A/G]CTGCCCGCTGTGTCT | 57602 |
rs560968879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825212 | AAGCATGCAGGAAAC[A/G]TTCACAAACGCTGGT | 57602 |
rs560972897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816051 | TGCCTGGCATGGCAG[A/C]TGTAGGCTGAGTGCA | 57602 |
rs561079254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802738 | AGGGAAAACCAGTCG[C/G]GTTTCCCATCCTAAC | 57602 |
rs561210814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811403 | TACGTATGCATATAC[A/G]CATATTTCTATTTCT | 57602 |
rs561216450 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795746 | AGGATGGGACACAGA[C/T]CTCTGCACACACACA | 57602 |
rs561220117 | snp | G/T | 3.295e-05 | 0.00405881 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836129 | GTCTCCTGGCCGGTG[G/T]GTCATCTCCACTCTT | 57602 |
rs561255045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821310 | GCTGACCACCACGTG[C/T]GGTACTCTCCTGCTG | 57602 |
rs561383262 | snp | A/G | 0.103082 | 0.202275 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836797 | TGGTTATACACACAC[A/G]GACACACACACACAC | 57602 |
rs561444088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837965 | TGGCCTGGGCCTGTC[A/G]TCCCAGATGCTTGGG | 57602 |
rs561500481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838309 | CACGGGAGGCAGAGG[C/T]TGGAGTGAGCCGAGA | 57602 |
rs561570299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826782 | TCCTAAAGTTATAAA[A/C]CTCCTCATGTTAAAG | 57602 |
rs561707796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812732 | AAGAAAAGAAAAGAA[A/G]TAACATCAACTAGAA | 57602 |
rs561723352 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809798 | GGCTAATTTTTGCAC[-/T]TTTTTTTGGAGATGG | 57602 |
rs561847264 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809929 | TCAGCTCACTGCAAC[C/T]TCCACCTCCCGGGTT | 57602 |
rs561920009 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835821 | ACATGCAGCCCACCC[C/T]ATTTCTCTTTCTTAG | 57602 |
rs561921150 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817330 | CGACATTAAGAATCT[C/G]CAAACACATTTGAGA | 57602 |
rs561946464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78799823 | AAATAACCCACTGGG[A/G]AAGCAATCGCACACC | 57602 |
rs561997284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827917 | CTCTATCTCAGAAAG[A/G]AAAAGAATAAAGAAT | 57602 |
rs562083288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799296 | CTCGTCTGAGGAACA[A/C]AGATGTCATGTTTGG | 57602 |
rs562133721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793595 | CACAGAAAGCTGCCC[A/G]TCTGCATGTCACGTG | 57602 |
rs562214422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809348 | CCTACATTCTATTCT[C/T]TGTTAATACTGTTTT | 57602 |
rs562248206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814738 | CAGGGGGATCACCTC[A/G]AGGAGTTCGAGATCA | 57602 |
rs562267963 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836208 | CTTTAAGGCCTCCAG[C/T]TGGTAGGAGAAGCTC | 57602 |
rs562280023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800622 | TCTCATCCACACAGC[A/C]CAGGGACCCGGCCAT | 57602 |
rs562315039 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819232 | GACCTAAAGAAGAGT[A/C]AAGCAGAATTAAGAA | 57602 |
rs562353645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821582 | GCAGGCATGTGCCAC[C/T]GCGCCTGGCTGATTT | 57602 |
rs562398700 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78815629 | ATAGCCAACTGCTAC[C/T]GCAAGTAAGACTTTT | 57602 |
rs562427112 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78840146 | CCCCGAGCATGGCTC[A/C]GTGGCGAGCGTTACG | 57602 |
rs562499468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805930 | GACAGAACTAAGACA[A/T]CAGGACTGCAGAGGC | 57602 |
rs562504714 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78789139 | GAGGCAGAGGTTGCA[C/G]TGAGTCGAGATTGCG | 57602 |
rs562585993 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78824302 | GCAAGAGAGAGAGGA[C/G]AGGAAAAGAGCTAGG | 57602 |
rs562588757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78815832 | ACACATGCACACATA[C/T]ATACATACACACACA | 57602 |
rs562592209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834502 | GGCTGGAGTGCAGCG[A/G]CATGATCTTGGTCAG | 57602 |
rs562695543 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78802298 | GCACACCCATGCGGT[-/C]TCCCACCCCCTCGCC | 57602 |
rs562807610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824641 | AGAAAAATCAGAAAT[A/G]AGCACAGTAAATATG | 57602 |
rs562821394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817213 | CTGGCTCCGTCATCT[A/G]CGTCTGTGTAAATGC | 57602 |
rs562864371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830364 | ATCTTCCAGCTAGAA[C/T]ATTTCACTGAATGAA | 57602 |
rs562873446 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840838 | CCGGCGCCTCACACA[C/G]GTGTCACCGCGACGC | 57602 |
rs562880320 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78838327 | GAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 57602 |
rs562971381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810866 | ATGCCTGTATCCCAG[C/G]ACTCTGGGAGGTCAA | 57602 |
rs562995099 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841326 | GCCTTAACGTCCCGG[G/T]CTCTGGGGCCATCCG | 57602 |
rs563008663 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842742 | GGGAGCGGACCAGGT[A/G]ATTTTTGGGTGACAA | 57602 |
rs563028402 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792888 | GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 57602 |
rs563083231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78801557 | TGTGTTCTGTGGCGG[A/G]TGCCTGCCAAGGCAT | 57602 |
rs563165997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820752 | AGCGTTGTTCCTGTT[A/C]ATGCTTCAGGACACA | 57602 |
rs563201058 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817557 | CTCAGGAGTTCGAGA[C/T]CAGCCTGGCCACCAT | 57602 |
rs563222728 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790986 | ATGAAAACACGCATG[C/T]AAGACATGTATCGTG | 57602 |
rs563247199 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837892 | GGATCATCTAATTCT[A/G]TACATGGATCAAGTA | 57602 |
rs563274881 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78830450 | CTCTGCTATCATAGA[A/C]ATTTTGCAATGAACA | 57602 |
rs563329178 | snp | C/T | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78816516 | TTGTGGTCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 57602 |
rs563331915 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP36 | GRCh38.p7 | 17:78798180 | CACACGCATCCCACA[C/T]ACACCCCCTTATACA | 57602 |
rs563413997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78828509 | CAAAGGAAAAGCTAC[C/T]TGTCCTGACCTGCCC | 57602 |
rs563426045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818147 | GTTTTTCTAAACTCC[A/G]TATTTCATAAAAAGC | 57602 |
rs563430515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78802135 | ACGCGGTCCCCCAAC[C/T]CCTCGCCTGGTGCAC | 57602 |
rs563476903 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798456 | GGCAGCCTTTGCTGG[A/G]TGAGTCACAGACCAG | 57602 |
rs563478930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78798785 | CCGGACAGGCCTGGG[A/C]AGCCTGGCTCTTCTC | 57602 |
rs563493220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837802 | AACAAGTCAAGTGTG[A/C]CCCAAAATTCTGCTC | 57602 |
rs563515862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78811573 | CTCACATTTTCCCCG[C/T]TAAATGTGAGAACAG | 57602 |
rs563529475 | snp | C/G | 0.000511302 | 0.0159809 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803462 | CCTCCGCTTCCTGCT[C/G]CTCGCGTGGTGGCCG | 57602 |
rs563564436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792886 | AAGCCCAGCTAATTT[C/T]TGTATTTTTAGTAGA | 57602 |
rs563611641 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796535 | AGAAAATCCAAAAAG[A/C]GACACCCACCCACAT | 57602 |
rs563654703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826827 | ATATACATGTACATA[A/T]AAATTATACTGCAGA | 57602 |
rs563656397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78817780 | AAAGAAACACATCTT[C/T]TATGAAAATGCCACT | 57602 |
rs563719619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808411 | GTAGACCACCACACC[C/T]GAATAATTATTACTA | 57602 |
rs563723588 | in-del | -/GAA | 0.00266723 | 0.0364212 | intron-variant | USP36 | GRCh38.p7 | 17:78818783 | TCTTCTTGCATCTAT[-/GAA]GAAGGTGATGAGAAA | 57602 |
rs563793369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78832215 | CTAGCTAAATATTAG[C/T]GCCAGAGACAGTCCA | 57602 |
rs563805154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808750 | TTCTGTATTTAGATG[C/T]TGAATGTCAGCCTTC | 57602 |
rs563837961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832907 | TAATCTCAGCACTTT[C/T]GGAGGCAGAGGCAGG | 57602 |
rs563874585 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788046 | TCTGGCACTGTGAGA[G/T]AACATTCCCATTGTC | 57602 |
rs563875100 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787077 | GCCTCCCAGGTTCAA[A/G]CGATTCTCATGTCTC | 57602 |
rs563898999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833252 | CAAGATGTTTACAAA[C/T]ACTTCCCACTGCATG | 57602 |
rs563935174 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | USP36 | GRCh38.p7 | 17:78821929 | GTAGAACAAACGTCT[C/G]CACTTACCGCGTGAT | 57602 |
rs564037161 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78795118 | AGAACCCCCTCAACC[A/G]CTGCCCAGGCTACAA | 57602 |
rs564116537 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78799324 | TGGTCTCGAAGTCTG[A/C]ATAAAAACATGCTCT | 57602 |
rs564128552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78804718 | TAAAAGGCAAAGTTA[A/G]TAAGAATTGTTCCAT | 57602 |
rs564172484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78804178 | TATTTAAATGCAAAG[C/T]TGGCCAGGTACAGTG | 57602 |
rs564242405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838382 | GTCTCAAAAAAAAAA[A/C]AAAACAAAAAACAAA | 57602 |
rs564268586 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78797918 | CTGACAGAGAGAAAC[A/G]AGACCCGAATCTTCC | 57602 |
rs564274157 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant | USP36 | GRCh38.p7 | 17:78798904 | TCAGCATCACACATC[A/C]TACCTTCCCTCGGTC | 57602 |
rs564371060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823596 | CCACCCGGAATCACA[C/G]CTGCAAAGGGCACCC | 57602 |
rs564445034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798825 | CGCTTCATGCCACTG[C/T]CGCCACCTCCAACTG | 57602 |
rs564485003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794651 | AAAGCCTGTCAGGCG[C/T]GGTGGCTCACACTTG | 57602 |
rs564510727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810762 | TGTGAAAGGCCCTGA[C/G]TGCCTGTGTGTGGGG | 57602 |
rs564523312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814899 | GAGGTTGCAGTGAGC[C/T]GAGATCGAGCCACTG | 57602 |
rs564526878 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795971 | CCTAGAGTTTGAACT[C/T]GTTTTCTGGGCCTCA | 57602 |
rs564527685 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840730 | CCCGACCCGACCCCA[A/G]CCTACCCCGGCCTCT | 57602 |
rs564532010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818897 | TGGAATCTTCATCAA[C/T]GAGATTTCGACCTTC | 57602 |
rs564592233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805957 | AGGCCGAACTGCCTT[C/T]ACCACCCAAAGCTCC | 57602 |
rs564623119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834524 | CTTGGTCAGCTCACT[A/G]CAACCTCCACCTTCT | 57602 |
rs564654931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839733 | AACATTAAGCAATAA[A/C]CTAAACAACGCTCGC | 57602 |
rs564664085 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796607 | CCATCTACACGCCAG[G/T]AACCACCCAGGCCCC | 57602 |
rs564707284 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802582 | TGAGCAAATTGGAAG[A/G]GGAGCAGGAGCGCAC | 57602 |
rs564711709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815291 | GAGCCGAGATCATAC[C/T]ACTGCACTCCAGCCT | 57602 |
rs564753419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789900 | TGCAGTGTGGACTGC[A/G]GAGCCACTGACTTTG | 57602 |
rs564790409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78810397 | GGCTCAAGTGATCCT[C/T]CCACCTCAGCCTCCT | 57602 |
rs564840324 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836563 | TGGACATATTAGTTC[A/G]CATTTCCCCCACAAA | 57602 |
rs564886737 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78801122 | GCTGGGACTAGAGGC[A/G]CCCGCCACCATGCCT | 57602 |
rs564959822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824749 | GGGGCTTAACCTGCC[A/T]ATTAAAAGATGGTCA | 57602 |
rs564996513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78829940 | GAGACAGAGTTTCAC[C/T]ATGCTGGCCAGGCTG | 57602 |
rs564996527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78824333 | AAGTAAAGGGTACCA[C/T]GGTGGACTGCCAAAT | 57602 |
rs565014375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78830440 | TTTCCATTTTCTCTG[C/T]TATCATAGACATTTT | 57602 |
rs565076095 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825479 | CCGACATCTGGTGAG[C/T]CTTCATCTCTCCCCT | 57602 |
rs565086071 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841373 | AGCACCTGCAGTTTG[A/G]GGAGGGAGGGATCTG | 57602 |
rs565105265 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809383 | AAGGAATTCATCTTT[C/T]CACTGCACCGCAAAG | 57602 |
rs565139862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815998 | GTGCACACACATATA[A/T]ACATACATGCACACA | 57602 |
rs565176827 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78831011 | GCAGGTGGATCGCGA[A/G]GTCAGGAGGTTGAGA | 57602 |
rs565252095 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78793021 | CGCCCGCCCCCCTCA[-/C]CCCCCCCAGGAAGGC | 57602 |
rs565343238 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797282 | TCTCCAGGACAGTTG[A/T]GAGCTACTCACAAGG | 57602 |
rs565356777 | snp | C/T | 1.65425e-05 | 0.00287593 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836062 | TAAGTCCATCCACTT[C/T]GTCACCCCGGAGTGA | 57602 |
rs565395148 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842172 | TGGGCGCCTGTAATC[C/G]CAGCTACTCAGGAGG | 57602 |
rs565400734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821138 | GACCGAGACCCAGCA[A/G]GGAGGCAGACTCTCA | 57602 |
rs565463331 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842373 | GAGGCCGAGGCAGGC[A/G]GATCGCTTGAGGTCA | 57602 |
rs565465051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78797987 | AATGCATGGCATCTC[A/G]ATGCGGCTGGCAAGA | 57602 |
rs565606144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791431 | GCCCTGGCCTTCTTT[C/T]TATAGGAAGTCATGA | 57602 |
rs565728860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811190 | TCCACCCCACTTCAA[A/G]TGATCACTGTGTTCT | 57602 |
rs565742776 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812622 | GGGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 57602 |
rs565755760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836455 | TCTCCTCTTTGGTCA[C/T]TATGGATGCTAGCCA | 57602 |
rs565802158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798214 | GCATCCCACACACAC[C/T]CTTCTCCAAGTGACT | 57602 |
rs565819164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78831396 | GGCGGGTGGAACACG[C/T]GAGGTCAAGAGTTCA | 57602 |
rs565850806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831815 | TTAGCTGGGCATGGT[A/G]CTATGAGTCTATAGT | 57602 |
rs565919883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808011 | ACCTGGCCTGAATAC[A/G]TATCTTTATGGCCAC | 57602 |
rs565977785 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP36 | GRCh38.p7 | 17:78821309 | TGCTGACCACCACGT[A/G]CGGTACTCTCCTGCT | 57602 |
rs566003268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817789 | CATCTTCTATGAAAA[C/T]GCCACTATAGGCCAG | 57602 |
rs566086265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827642 | GTGAGGTGGCTCACA[C/T]CTGTCACTCTAACAC | 57602 |
rs566114009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821612 | TTTGTATTTTTAGTG[A/G]AGACGGGGTTTCACC | 57602 |
rs566226716 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78822898 | TGCGCCGGTGCACCC[A/G]CTCCCTCCAGAAGAG | 57602 |
rs566290169 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826676 | AACCTATGAACTCAG[G/T]AATGACACAAAGACA | 57602 |
rs566393881 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP36 | GRCh38.p7 | 17:78838140 | GTAATCCCAGCACTT[A/G]GGAGGCCGAGACGGG | 57602 |
rs566457304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793085 | TTCTGATTCTACTTC[C/T]GTCAGTATCGAATGC | 57602 |
rs566472853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798693 | CACAATGACCCCTGT[A/G]CACGGCGACCTGCAG | 57602 |
rs566495385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839014 | CACCTGCCAGTCAGC[G/T]CCAGTCTAATCTTAT | 57602 |
rs566514264 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791851 | TGTAATCCCAATGCT[C/T]TGGGAGGCCAAGGCG | 57602 |
rs566539580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828567 | AGCCCACATGTCTCT[A/C]AACTGCTATTCCTTG | 57602 |
rs566552370 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823355 | ACCACCCCCACAACC[C/T]CTCTGTCATCCAGAA | 57602 |
rs566602904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78805814 | CTTCGCCTTTCTCTT[C/T]GACTGGGAAGTACTG | 57602 |
rs566664752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78787871 | AAACAGGACTTGTGT[C/T]CTTACAAAAAGAGGG | 57602 |
rs566675677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78818934 | TCTCAAAATCACATT[A/C]AGCATGCCTCAAGTA | 57602 |
rs566759486 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837584 | AACTGTAACCAAGAA[A/G]AGACCCCTGCACCTC | 57602 |
rs566798005 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78814776 | CAATATAGCGAAACC[A/C]CACTTCTAATAAAAA | 57602 |
rs566843487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834073 | CCAACATGGTAAAAC[C/T]CCATCTCTACTAAAA | 57602 |
rs566852981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805224 | AAACTATAAGGGCCA[C/T]GCCAGCTGCACGATG | 57602 |
rs566858134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78788819 | TGTCATTCCCCTCCA[C/T]CAAGGCCAGAATGCT | 57602 |
rs566861999 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78808582 | ACATTTTACTATATA[A/T]ACTATGTACTACTGA | 57602 |
rs566864371 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814359 | CGCATCTGGATGTGC[A/G]TGGGTGCTGAAACCT | 57602 |
rs566904514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814989 | AAGACAATTTGGGGC[A/G]AATGGGTGTGCAGCA | 57602 |
rs566927003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799610 | CATTCCACACCCTTC[C/T]CTCCTACAAAACCAA | 57602 |
rs566940391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805717 | TGAGACAGTTCTTAA[C/T]CTGCATGACGCTAGC | 57602 |
rs567000917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834508 | AGTGCAGCGGCATGA[C/T]CTTGGTCAGCTCACT | 57602 |
rs567010986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834571 | CCTGCTTCAGCCTCC[C/T]GAGCAGCTGGGATTA | 57602 |
rs567188337 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796062 | ACAGTGATAAACGCT[G/T]CAGAAAGTCATCTCG | 57602 |
rs567217359 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799182 | AGGAGGACGGCTCGA[C/T]GCCCATGTGTGGTCG | 57602 |
rs567270865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815734 | CACGCACACATATAC[A/G]TAACATGCATACATA | 57602 |
rs567283751 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834331 | CTTTAATTTCTTTAA[C/T]AGTTAAAAGACTCTT | 57602 |
rs567295479 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78840349 | GGCCGCACCCGCCCC[G/T]CTGAGCTCTGCGGCC | 57602 |
rs567313524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815865 | TATGCATGCATACAC[A/G]TGTACGCATATACAT | 57602 |
rs567338222 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP36 | GRCh38.p7 | 17:78827957 | GGCAGGATGCAATGG[C/T]TTATGCCTGTAATCC | 57602 |
rs567415046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820845 | AAAACAGGTAAAGAC[A/G]ATGGTCTGTACTGCA | 57602 |
rs567440674 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840977 | TTCCGTGTCGCCTAC[G/T]TCACCTCCCCATCAC | 57602 |
rs567443854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830217 | CACACATGTGTATCC[A/G]TGAACAATAAATGGC | 57602 |
rs567595551 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841492 | GGTGGCGGCTGTGCA[A/G]TCTCTAGCTCCACCC | 57602 |
rs567605488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830625 | TATCAAATAGATCCA[G/T]CTCATAACACAAAAC | 57602 |
rs567634104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826035 | CTCAGTTCCCAGTGC[A/T]AGCTATGGGGCCCAG | 57602 |
rs567637833 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP36 | GRCh38.p7 | 17:78816637 | TCTCAAAAAAAAAAA[A/C]AAAAAAACCAAAATT | 57602 |
rs567645049 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797359 | AGGTGGCTGGGTGGG[C/G]TCACCTCTTCCTTTC | 57602 |
rs567688547 | snp | C/T | 0.00080016 | 0.019986 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836548 | CCAGCACTAATCACT[C/T]GGACATATTAGTTCA | 57602 |
rs567725127 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842542 | GGTGGAGGTTGCAAT[A/G]AGCTGAGATCGTGCC | 57602 |
rs567777006 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793614 | GCATGTCACGTGACC[A/T]GTCCACACACAGTCC | 57602 |
rs567947097 | snp | A/G | 0.00013308 | 0.00815613 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807516 | AAGGGGACCCCGAGG[A/G]CAGCTTTGGAGGAAT | 57602 |
rs568120010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832356 | CCACAGCCAAAGCCC[A/G]CTTAGGGGTCACTCA | 57602 |
rs568261440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798608 | TCTTTCCTGGCCCAC[A/G]GGGCTCCATGCTGCA | 57602 |
rs568283520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78827446 | GGCTGTTATAAGGGG[A/G]AAATACTGCAACTTT | 57602 |
rs568301231 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78804417 | AGTGAGCCGAATCGC[A/G]CCACTGCACTCCAGC | 57602 |
rs568356132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822151 | GTCACCACAGACCCT[C/T]AACCTCCATCCTCAG | 57602 |
rs568387504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799175 | GGACAAGAGGAGGAC[A/G]GCTCGACGCCCATGT | 57602 |
rs568464776 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78831437 | GGCCACTTGGTGAGA[A/C]CCCCATCTCTACTAA | 57602 |
rs568494833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808069 | TCAAGATTTGGGAAG[A/T]GAAAAAAGTATAAAG | 57602 |
rs568497158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817995 | GAGGCTAAGGCAGGG[A/G]GATCGCTTGAGCTTG | 57602 |
rs568522663 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | USP36 | GRCh38.p7 | 17:78799566 | AGCCGAGCGATGCCC[A/C/G]CCCGCCACACTCACA | 57602 |
rs568588280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818300 | CACAACCAGAAGCTG[C/T]GGTAAATCCATTAAG | 57602 |
rs568603784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78818998 | AAAGTGGGAAGATTC[C/T]AAAGCAAAAAAATAA | 57602 |
rs568607576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808487 | AATTCCTGAGCTCAA[A/G]CAATCCTCCCACCCT | 57602 |
rs568640267 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838611 | GCAGACTTGGGCCTG[C/G]TGTCCTACTGCGGCA | 57602 |
rs568724433 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790297 | GTTTCTTTTTCTTTT[G/T]CTTTTTTTTTAAAGA | 57602 |
rs568739495 | snp | A/G | 4.95946e-05 | 0.00497944 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814539 | ATGTTGAGGAATTCC[A/G]GATAGCCTACATCCT | 57602 |
rs568764372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833372 | ATGCAACCTCTGCCT[A/C]CCAGGTTCAAGTGAT | 57602 |
rs568803421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832992 | CGTCTCTACTAAAAA[C/T]ACAAAATTAGCCAGG | 57602 |
rs568886355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834119 | AGGCGTGGTGGCGTG[C/T]GTCTATAGTCCCAGC | 57602 |
rs568896224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78787918 | CGGAAAGATGGCTAC[A/G]TGAAGATGGAAGCAC | 57602 |
rs568917488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823865 | GGCAGACAGAGGAGG[C/T]GCTCTGGATACGAAT | 57602 |
rs568922661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839867 | TCTCTCTTGTCCAAG[G/T]ACAGCACAGGCCTCA | 57602 |
rs569067441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78830107 | TGATCGCCGAACTCC[C/T]CTCAATCTCTCTCAA | 57602 |
rs569130534 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788667 | AGAAGGCATGAAGGA[A/G]GGAAGGGCCAAGGAC | 57602 |
rs569180290 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792092 | AATCCTGGGAAGAAG[A/T]CGGTGGCAAGAGTGG | 57602 |
rs569249924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78831537 | AGAATCGCTTGAACC[C/T]GGGAGGTGGGGGTTG | 57602 |
rs569252229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78800384 | CATCAGCAACACCGC[A/T]CAGGTCCACCCAGCA | 57602 |
rs569275935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78809971 | CCTACCTCGGCCTCT[C/T]GAATAGCTGGGATTA | 57602 |
rs569286642 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78813660 | TGACACATGACAAAT[C/T]CCTCCAGTGGAATTC | 57602 |
rs569476043 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796183 | AGGAGAGAAGGGAGA[C/G]AAAGGAACGAGATAA | 57602 |
rs569525149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820416 | TACAGTGAGCTATGA[C/T]TGCGCCACTGCACTC | 57602 |
rs569555846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824972 | AATGAAGACATGACA[A/G]TTACGAATATCTAAC | 57602 |
rs569570212 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP36 | GRCh38.p7 | 17:78790111 | TTTTTTTTTTTGAGA[C/T]GAAGTCTCGCTCTGT | 57602 |
rs569575297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820190 | GAGACAAGAAATGAA[A/T]GCAGCCAGGAACAGC | 57602 |
rs569678575 | snp | C/G/T | 5.35674e-05 | 0.00517507 | intron-variant | USP36 | GRCh38.p7 | 17:78803348 | TGCTTTGTTTCTCGT[C/G/T]AGAGGTAGACAGATG | 57602 |
rs569697240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815881 | TGTACGCATATACAT[A/G]CATGCACAACACATA | 57602 |
rs569698207 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841075 | GGCAGGGTGACGTCT[C/T]CGCAGCGCACTAGAG | 57602 |
rs569786322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810576 | TGAGTCACAGTCCCA[A/G]GCCCAGGCTGCTTCC | 57602 |
rs569810361 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78802304 | CCCATGCGGTTCCCA[A/C]CCCCTCGCCCGGTGC | 57602 |
rs569842708 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841611 | AAAATCCTCTTGATC[C/T]GAGGCAACTTCGCTG | 57602 |
rs569942590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811760 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 57602 |
rs569964045 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP36 | GRCh38.p7 | 17:78831189 | CAAGATCACACCACT[A/G]CACTCCGGCCTGGGC | 57602 |
rs570030903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812541 | AAAAATACAAAAAAA[A/G]TTAGCCGGGCGTGGT | 57602 |
rs570087931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832034 | AGGTTCTCCAGCAAT[A/G]TATGAGATTAATTTA | 57602 |
rs570249431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78832373 | TTAGGGGTCACTCAG[A/G]ATCCAGTGGGGTGCA | 57602 |
rs570273919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828018 | CGCTTGGAGCTGGGA[C/G]TTGGAGACCAGCCTG | 57602 |
rs570283395 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78788517 | CCTTTATGTTCTCCC[A/C]GCTGGTTGGTGGGGC | 57602 |
rs570396823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78807899 | GACAGAGATGGGGTT[G/T]CACCATGTTGGCCAG | 57602 |
rs570438015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837405 | CCCCGGGAGGTTCTA[A/T]CATCCTTAGCTATGA | 57602 |
rs570464636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78803079 | GAGTAGCTGGGACTA[C/T]AGGTGCATGCCACCA | 57602 |
rs570496624 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78806747 | CATGAGCATCACCAG[A/G]TCAGGGCTCTCTCAA | 57602 |
rs570524511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798644 | GTCCTGCACACAGGC[C/T]GGGCTCTCATGAGCT | 57602 |
rs570643623 | snp | A/G | 1.66189e-05 | 0.00288256 | intron-variant | USP36 | GRCh38.p7 | 17:78814387 | CCTGTCCCAGGAGGC[A/G]GCTGCACTGACACAA | 57602 |
rs570646280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818418 | CAAATTCACTGGCAC[C/T]GGGATAAACCCAGAA | 57602 |
rs570662477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793012 | TGAGCCACCGCGCCC[A/G]CCCCCCTCACCCCCC | 57602 |
rs570680744 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787219 | GACCTCAGGTGATCT[A/G]CCCACCTCAGCCTCC | 57602 |
rs570681644 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838552 | GCAGACAATTCAACG[A/G]AATCAAAAAATACAC | 57602 |
rs570842457 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831656 | ATTATATATAAAACG[C/G]TGCTGGTTGGGCATG | 57602 |
rs570847801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838898 | GCACTCAGGATGAGG[C/T]GGGTGGACCGTACTA | 57602 |
rs570857382 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808111 | GCAAAGTTCCATCAC[C/T]TAAACATAACCATGC | 57602 |
rs570879109 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78804547 | GATAGGTGCAGCAAA[A/C]CACCATGGCACCTCT | 57602 |
rs570912557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794987 | CACTCCAGCCTGGGC[A/G]ACAGAGGGAGACTCT | 57602 |
rs570971320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814275 | ACTCCACGCAGAGAG[A/G]CAACAACGAGGACTT | 57602 |
rs570971429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808584 | ATTTTACTATATATA[C/T]TATGTACTACTGATA | 57602 |
rs570998602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815192 | CAAAAATTAGCCAGG[C/T]GTGGTGGCACGTGCC | 57602 |
rs571101694 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793668 | GTACCCACATCCTCA[C/T]TGCGCTGAGGTTGTC | 57602 |
rs571123736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823386 | GCCCGCAAGCACCAG[C/T]GCCCGCAGGGCCACA | 57602 |
rs571160144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829225 | TTTGGAAGCTATGAT[A/C]CATCCAAAGCTGAAA | 57602 |
rs571255455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819551 | CACAGTCCCTGGGGC[A/G]GCCGCCCGGTGCCAG | 57602 |
rs571260949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829744 | GGCATTAGGCTAGAC[A/G]GTGGTCCTTTTTTTT | 57602 |
rs571304774 | in-del | -/AG | | | intron-variant | USP36 | GRCh38.p7 | 17:78831253 | AAAAAAAAAAAAAAA[-/AG]GGACAACATAAATAT | 57602 |
rs571308702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820104 | CTTTTTTAGGCTGAG[A/G]CAGCAAATCACAGAA | 57602 |
rs571384253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824999 | TAACCACAACCACCT[A/G]TATAGAGCAAAACTA | 57602 |
rs571439885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78834704 | CACCTCTGCCTCCCA[C/T]AGGTGTGAGCCACCG | 57602 |
rs571477049 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840481 | GCCCGGGGGACGGCG[A/G]AGACCGGCGAGGACA | 57602 |
rs571508842 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78840967 | CCACCGCCGCTTCCG[G/T]GTCGCCTACGTCACC | 57602 |
rs571593814 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78800855 | ACAACCAGCACCTGG[A/C]ATGGACCCTGGCGCA | 57602 |
rs571647418 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796322 | AGGAACATACCCTGC[C/T]CGTGAAGGCATGTGC | 57602 |
rs571677931 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791618 | ATTTCCTCAATGCCT[C/G]GAGTGCTTTCTGAGA | 57602 |
rs571683227 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796772 | CATCTCCACCTGCGA[C/T]GACTCCGGGAGGAAA | 57602 |
rs571712477 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841124 | CGGCCGAGCACACCT[G/T]GCGGCGTGGCGGACG | 57602 |
rs571861615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790799 | CTTAGACTGTGTGTT[A/G]AAATCTGGTCTCATG | 57602 |
rs571904524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78791122 | TCTTGATTCCCAATC[C/T]GGCCTTCTTTTTTTT | 57602 |
rs571933537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820824 | GCTTAGGAAAAACTC[C/T]AGAAAAAAACAGGTA | 57602 |
rs571952518 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78835019 | TATATATATATATAT[A/T]TTGGAAGTATCTTTT | 57602 |
rs571991621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78801228 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGTT | 57602 |
rs572009070 | in-del | -/AAAAAA | 0.150333 | 0.229274 | intron-variant | USP36 | GRCh38.p7 | 17:78812698 | CGAGACTCTGTCTCG[-/AAAAAA]AAAAAAAAAAAAAAA | 57602 |
rs572079109 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797121 | AATGGAGAATTCTAC[C/T]CCAAAGCCTCCACCT | 57602 |
rs572120987 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834863 | GCTCACACTTATAAT[C/G]CCAGCACTTTGGGAG | 57602 |
rs572131998 | in-del | -/TAGAGAGATT | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78832127 | ATGACTACACGGACA[-/TAGAGAGATT]TGGGAAACAAAAGGA | 57602 |
rs572154529 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797452 | GGACACAACGGTGGC[A/G]TCAGCCCCGAGAAGC | 57602 |
rs572169318 | snp | A/G | 8.33618e-05 | 0.00645554 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807244 | GAGGCCAGCGCTCTC[A/G]TCGTTCCCCTTCAGC | 57602 |
rs572184331 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805540 | TTTCACTGCTTCCGT[C/G]CCCACTCCCAGCGGC | 57602 |
rs572200254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830272 | TCCTTTCTATAAATC[A/G]TATCATGCAGTTACG | 57602 |
rs572227698 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830061 | TGGTACATTTTTACC[C/T]TTCAAATTATGATGT | 57602 |
rs572232460 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807071 | ACCGTCTTAGAATCT[A/G]CTCCACTTGGCGGCG | 57602 |
rs572364522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821210 | AGCATCCTGGTGTCC[A/G]AACAGAGAGCTCTCT | 57602 |
rs572449805 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842196 | CAGGAGGCTGAGGCA[C/T]GAGAATCCCTTGAAC | 57602 |
rs572471399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78812062 | GGTGTGGTAGTGCAC[C/T]GATAGTCCCGAATAC | 57602 |
rs572513726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837563 | CTGTTGGTGCAGCTG[C/T]ATGGAAACTGTAACC | 57602 |
rs572553465 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811592 | ATGTGAGAACAGGCC[A/G]GGCACAGTGGCTCAC | 57602 |
rs572569137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78831577 | GAGACTGTGGCAACT[A/G]CACTCCAGCATAAGC | 57602 |
rs572604683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836647 | AGCCAGACAGCCCCT[A/G]CCATGTGCATCTCTT | 57602 |
rs572611961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78822541 | TCTCAGAGAGGACAG[C/T]GGAGTCAGACGTGGG | 57602 |
rs572682524 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800999 | TTTTTTTTTTTGAGA[C/G]GGAGTCTCACTCTGT | 57602 |
rs572701529 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820554 | GATGATCTTGTAGCT[A/G]GACCTGCTCTGGAGC | 57602 |
rs572748280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792277 | TTCCTAAGGGAAGAG[A/T]GAGACACGGGAGCAG | 57602 |
rs572817883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78798223 | ACACACCCTTCTCCA[A/C]GTGACTAGGACACAC | 57602 |
rs572833284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790163 | GCGCGATCTCAGCTC[A/G]CTGCAACCTCGGCTT | 57602 |
rs572846808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78838297 | GAATTGCTTGAACAC[A/G]GGAGGCAGAGGTTGG | 57602 |
rs572857387 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78835754 | GAGGACACAGCTCAG[A/G]GACTGAGTGGCGGAA | 57602 |
rs572902685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78817627 | AGGTGTGGTGGTGGG[C/T]GCCTTAATCCCAACT | 57602 |
rs572910217 | snp | A/C/G | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838743 | AGCCGCAGAGCGGGC[A/C/G]TCAGAGCCTGTGGGA | 57602 |
rs573094352 | snp | A/G | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786994 | TATTTATTTTTTGAG[A/G]CTGAGTCTCGCTCTG | 57602 |
rs573099046 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78788172 | TTATTTTATTTATTT[A/T]TTTTTTTTTTTGAGA | 57602 |
rs573132359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78808625 | GTATGGTTAATTTAT[A/G]TAAGCTATATTGTCT | 57602 |
rs573227399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78793966 | CTCACCACCTGAAGG[C/G]CTTCCTGAAACCATC | 57602 |
rs573258267 | in-del | -/A | 0.236144 | 0.249616 | intron-variant | USP36 | GRCh38.p7 | 17:78831943 | GTGAGAGCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 57602 |
rs573279352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828840 | CGAGAACCCCATCTC[C/T]ACAAAAAATTAAAAA | 57602 |
rs573286433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78828368 | TGAATGAGACTTTTT[C/T]ATAGCATAGGCAACT | 57602 |
rs573324635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78804615 | CTTAAAATAACTGAT[C/G]CCTGAGATTTAAAAA | 57602 |
rs573342543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78812577 | CACCTATAATCCCAG[C/T]TACTAGGGAGGCTGA | 57602 |
rs573360124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805896 | ACCACAAGGATGTCG[C/T]AGACAGACCACCAAC | 57602 |
rs573377542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833810 | TGTTCGTGAAGAAGT[C/T]GTGGTTATCCATTTT | 57602 |
rs573425174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805431 | ACGCACAGTCATACC[A/T]CGCCCTCATGTAGCA | 57602 |
rs573430060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823408 | AGGGCCACAAGGAAT[A/C]CCCTCTTGCATAACC | 57602 |
rs573455212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78814691 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 57602 |
rs573487866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78800936 | GCTCCGAGGGTGGCA[C/T]GGAGCACAGCTCTGG | 57602 |
rs573540694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792525 | TGCCCAGCAGCAGCC[A/C]CGGGGACTATTGGAC | 57602 |
rs573549330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP36 | GRCh38.p7 | 17:78800533 | TCTGACCTCATTTCT[C/T]CCTGCCTCCAATTCC | 57602 |
rs573562443 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78823000 | GGGCTGTTTCCAGGG[-/CT]CTCTCCACGTTTCCC | 57602 |
rs573578222 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806804 | TAGCCGTTCTTTAAT[A/T]GCAAATGGCTGGGAA | 57602 |
rs573584967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819228 | AACAGACCTAAAGAA[A/G]AGTAAAGCAGAATTA | 57602 |
rs573587911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809322 | ATTTTCTTCCAAGTT[C/T]TGTTTTGTTCCCTAC | 57602 |
rs573630301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824194 | GTGGGCAATGAGCAA[C/T]GGGAAGATGTAACCA | 57602 |
rs573662280 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78839497 | TATCACTGCTTTCGG[A/T]TAGGACTCACATCTA | 57602 |
rs573713305 | snp | A/C | 1.65097e-05 | 0.00287308 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798533 | TCTTCTCTCTCTTAA[A/C]TTTTTTAATTTTCTT | 57602 |
rs573718819 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794452 | CCCACGGTGCTTCAG[A/G]CAGAGCTCATGACAG | 57602 |
rs573724123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78829436 | TTTAGGGCTGACAGC[C/T]CCTTAGTAGTGCCTC | 57602 |
rs573764366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78834467 | TGTGTGTGTGAGATG[A/G]AGTCTTGCTCTGTCA | 57602 |
rs573888875 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP36 | GRCh38.p7 | 17:78840511 | AGCCCGGCCCCGGAC[C/T]CTCCTCGGGAATACC | 57602 |
rs573908179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78825045 | GACAGGCACCCACCA[C/G]AATTCCAGTAATCAT | 57602 |
rs573948718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790337 | ACTCTGTCACCCAGG[C/T]TGGAGCACAATGGCG | 57602 |
rs574102110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78835877 | TATACTTGGGATAGG[A/G]GGACAGCAAGTCCAA | 57602 |
rs574165082 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817389 | TACCAGTGAGGAAAC[A/G]GAGGCTCAGCCAAGG | 57602 |
rs574180659 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837633 | ATCCACCACTTGCCC[C/T]CCCCTACCCACCACC | 57602 |
rs574216757 | in-del | -/ACAC | 0.0119256 | 0.0762928 | intron-variant | USP36 | GRCh38.p7 | 17:78815926 | TGCATACGCACACAT[-/ACAC]ACACATATACACACA | 57602 |
rs574272956 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78811342 | CATAACCTTTATCAT[A/C]CTCTCTCTGTATGTA | 57602 |
rs574344106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78802179 | CCCACCCCCTCGCCC[A/G]GTGCACACCCACGCG | 57602 |
rs574407886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78806709 | ACAGGGAACTGCTAC[C/T]TTGCCCAAACCTCCA | 57602 |
rs574474992 | in-del | -/AGAC | | | intron-variant | USP36 | GRCh38.p7 | 17:78830380 | TTTCACTGAATGAAG[-/AGAC]AGACCACTGTTATTT | 57602 |
rs574519887 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837644 | GCCCTCCCCTACCCA[C/T]CACCTCTCAACTTAA | 57602 |
rs574543837 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824398 | GCATTTCAAAAGGGC[C/G]TATGAAACCAGCAGG | 57602 |
rs574545654 | snp | C/T | 0.00014855 | 0.00861703 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803451 | GCTCCTTTCCTCCTC[C/T]GCTTCCTGCTGCTCG | 57602 |
rs574555754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792058 | GGAGCTCTCCAGGGT[A/G]CGGAGGTCAACAGTG | 57602 |
rs574564216 | snp | A/G | 2.52146e-05 | 0.00355059 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821036 | GTCGTAGGTGTCCGA[A/G]ACGCTCTTGCACACG | 57602 |
rs574600043 | snp | C/G | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840611 | CTGCGCGGACCCGCG[C/G]CCACGTTCTCCCTGA | 57602 |
rs574652713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78821355 | GAAGAGCTGCCTCCT[A/C]CCTGCACGCGTGCAC | 57602 |
rs574678528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP36 | GRCh38.p7 | 17:78798730 | TATTGACAAAGGGGC[A/G]GAAGCTGCGAGGATG | 57602 |
rs574731236 | snp | A/C/G | 4.94453e-05 | 0.00497198 | intron-variant | USP36 | GRCh38.p7 | 17:78798397 | CACCCCCTCGGAACC[A/C/G]ACCTCCTTCCACAGG | 57602 |
rs574737979 | in-del | -/AG | | | intron-variant | USP36 | GRCh38.p7 | 17:78832724 | CAGGCCTGGGATAGC[-/AG]AGTCTTACTGCCAAA | 57602 |
rs574790572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816847 | TATATAGATCAAAGA[A/G]TTTTGACAAGTATAT | 57602 |
rs574805840 | snp | A/G | 1.6528e-05 | 0.00287467 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807325 | GACAACATCCCTGCT[A/G]TCCCAGGAGCCCTGC | 57602 |
rs574896369 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816490 | ATTTAGCCAAGCATG[G/T]TGGCACACATTTGTG | 57602 |
rs574948112 | snp | C/T | 1.70644e-05 | 0.00292094 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827276 | GGCAGGCTTTCTGCA[C/T]GGCGTCGATGGTGTA | 57602 |
rs574952205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792782 | GGAGTGCAGTGGCAT[C/G]ATCTTGGCTCACTGC | 57602 |
rs574987949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813978 | AGTTGCTACATTTCC[A/G]AACACTATTAATAAT | 57602 |
rs574998122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78818590 | GCTATCAAACTCGTG[A/G]CTATCACTTTCTTCG | 57602 |
rs575000692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78813445 | GCATATCCCTACAGG[G/T]GCAGCTTCCCCACAC | 57602 |
rs575006262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78793241 | ATGGGAATTCTTGAG[C/G]TAGCCTTGGAAGTCA | 57602 |
rs575088100 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794332 | CTTCTTGTCCAAACT[G/T]TCAAACAAAACCTGC | 57602 |
rs575093284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78838204 | GGCGAAGATGTTTCT[C/T]TACTAAAAATACAAA | 57602 |
rs575096595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832165 | GACAGGACTGAACTG[A/C]GTTCCTCCTAGACTA | 57602 |
rs575117442 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789593 | TGGATTGGGGCATTG[A/T]CTTGCTTTGAAAACC | 57602 |
rs575142944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823018 | TCTCCACGTTTCCCA[C/T]GGCCACCCAGACCAT | 57602 |
rs575175541 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787343 | GCAAACAGGTTAACT[A/G]TATTAGGATACTTTC | 57602 |
rs575193163 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78839124 | CCTCAGGGAGTAATA[G/T]GAGTTGCCAAAATTT | 57602 |
rs575193288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833142 | GACAGAACGAGACTC[C/T]ATCTCCAAAAAACGC | 57602 |
rs575216381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78787671 | CATCTGTGAGGTAGA[A/G]ATTGGGAGCCACATT | 57602 |
rs575447374 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797427 | TGAGGAAGCAGGGGA[A/G]GGCGGGCTCGGACAC | 57602 |
rs575454536 | in-del | -/GATCCCCTGGATCAGC | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836494 | CTCCCCTGGATCAGT[-/GATCCCCTGGATCAGC]GATCCCCTGGATCAG | 57602 |
rs575511057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78808065 | TTCATCAAGATTTGG[A/G]AAGAGAAAAAAGTAT | 57602 |
rs575511676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78809163 | GTTGACAATATTTTA[C/T]AAGGTTTTATTGCTT | 57602 |
rs575627873 | in-del | -/AC | 0.00557542 | 0.0525036 | intron-variant | USP36 | GRCh38.p7 | 17:78813267 | ATGCACCAGAAAGCA[-/AC]AGAACCTCAAACACC | 57602 |
rs575683197 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP36 | GRCh38.p7 | 17:78801069 | GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC | 57602 |
rs575684124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78794618 | CCTAGTGTTTGGGAA[A/G]CGGCAGTTAAGAATG | 57602 |
rs575785197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78819276 | GCCTACAGCTTTACA[A/G]GGACCTAGATATAAA | 57602 |
rs575792029 | in-del | -/AAT | 0.00716266 | 0.059414 | intron-variant | USP36 | GRCh38.p7 | 17:78830887 | TATTTTTAAAATGAC[-/AAT]AATGATTGGTGAACT | 57602 |
rs575808828 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797050 | AAGGAAACATATTGC[C/T]AATGGAAGCCACAGG | 57602 |
rs575871023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78802030 | AAGCTCAGATGCAGT[A/G]GACGCTGCTCTCAGC | 57602 |
rs575912602 | in-del | -/A | 0.00318978 | 0.0398085 | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842309 | AAAAGAAAAGAAAAG[-/A]AAAAAAGGCAGGGCA | 57602 |
rs575976711 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP36 | GRCh38.p7 | 17:78840616 | CGGACCCGCGCCCAC[A/G]TTCTCCCTGAGCGTC | 57602 |
rs576010076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78815267 | AAACCAGGAGGTGGA[A/G]GTTACAGTGAGCCGA | 57602 |
rs576018833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810183 | GAATTCACCAGCGTG[A/C]TCATGGCTCACTGCA | 57602 |
rs576116634 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78811361 | TCTCTGTATGTATAT[A/G/T]TACGTGTGTATATAT | 57602 |
rs576130976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78810889 | GAGGTCAAGCTGAGC[A/G]AATCACTTGAGGTCA | 57602 |
rs576131156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78816307 | TGGGACTATAGGCAC[A/G]CGCCACCATGACTGG | 57602 |
rs576134385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78789843 | AGAAAAACAAAGGGG[G/T]TGCGGGTAGGGCTCA | 57602 |
rs576195451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | USP36 | GRCh38.p7 | 17:78835982 | CTGAAATCCACTGAC[A/C]CCATGTAAAAATTCA | 57602 |
rs576251315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78790453 | GTGCCACGAGGCCCG[C/G]CTAATTTTTTTTTAT | 57602 |
rs576263126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820630 | CTGCAGCAGGATGTG[C/T]GACAAAGCCAAGGCT | 57602 |
rs576315372 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78829891 | GACTACAGGCTCGTG[C/G]CACCATGCCAGGCTA | 57602 |
rs576349447 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810855 | CACGGTGGCTCATGC[C/T]TGTATCCCAGGACTC | 57602 |
rs576353872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78830959 | AGGCCAGATGCAGTG[A/G]CTCACGCCTGTAATC | 57602 |
rs576380648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78826626 | AGGCAATACAAGGAA[C/G]TCCTAAGCATTTCCT | 57602 |
rs576500393 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818314 | GCGGTAAATCCATTA[A/G]GACAGTGGCCCTGGA | 57602 |
rs576677638 | snp | C/T | 0.000700584 | 0.018703 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807228 | TGGAGCCCCTCCTGT[C/T]GAGGCCAGCGCTCTC | 57602 |
rs576690260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836564 | GGACATATTAGTTCA[C/T]ATTTCCCCCACAAAA | 57602 |
rs576731551 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78794627 | TGGGAAACGGCAGTT[A/C]AGAATGGAAAAGCCT | 57602 |
rs576768259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78820697 | CAAAGGCTGCACGCC[A/G]CCCAGAGCACACAAC | 57602 |
rs576847184 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804164 | ATTAATTCAACATCT[A/G]TTTAAATGCAAAGTT | 57602 |
rs576882022 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP36 | GRCh38.p7 | 17:78829785 | TCTCACTGTCACCCA[C/G]GCTGGAGTGCAGTGG | 57602 |
rs576887211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78792114 | CAAGAGTGGGAATTA[A/G]GTCACTGAGAAGTGA | 57602 |
rs576926177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78817553 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 57602 |
rs577002970 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787079 | CTCCCAGGTTCAAGC[A/G]ATTCTCATGTCTCGG | 57602 |
rs577089263 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787514 | GTATACATGCTACTC[A/G]TTTACAGGTGTATAT | 57602 |
rs577196991 | snp | A/C/T | 4.94931e-05 | 0.00497434 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803465 | CCGCTTCCTGCTGCT[A/C/T]GCGTGGTGGCCGTCC | 57602 |
rs577199598 | snp | A/C | 0.103438 | 0.202533 | intron-variant | USP36 | GRCh38.p7 | 17:78813110 | ACACGGCCTGGGGAA[A/C]CCCTGCCAGTCCTAA | 57602 |
rs577211858 | snp | C/T | 0 | 0 | intron-variant | USP36 | GRCh38.p7 | 17:78812658 | TTGGAGATCGCACCA[C/T]TGCACCCCAGCCTGG | 57602 |
rs577222312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP36 | GRCh38.p7 | 17:78798810 | CTTCTCATGCTCGGC[C/T]GCTTCATGCCACTGC | 57602 |
rs577225461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78792310 | AGGGTAATTAATGGA[A/G]CAAGGTCCCCAGGGT | 57602 |
rs577284191 | snp | C/T | 3.46386e-05 | 0.0041615 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803849 | GACCTGAGGCAGCGC[C/T]GTCGAGATGGAGGAG | 57602 |
rs577337039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78808116 | GTTCCATCACCTAAA[C/T]ATAACCATGCATTAA | 57602 |
rs577341960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78822657 | CTTCTCACCCGGACC[C/T]GGGGCTGCCTGGCGC | 57602 |
rs577342380 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP36 | GRCh38.p7 | 17:78814680 | TTTGGGGGCCGGGCA[C/T]AGTGGCTCACGCCTG | 57602 |
rs577358666 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790120 | TTGAGACGAAGTCTC[A/G]CTCTGTCATCCAGGC | 57602 |
rs577410141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78799188 | ACGGCTCGACGCCCA[A/T]GTGTGGTCGGTCAGC | 57602 |
rs577442137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78832644 | CACAAAGTTGGCAAC[C/T]GGCTCAAAAAGATCC | 57602 |
rs577467396 | snp | C/T | 1.65392e-05 | 0.00287564 | intron-variant | USP36 | GRCh38.p7 | 17:78818626 | TTCTGATGCCGACTG[C/T]GGCCCACGGAGCTGC | 57602 |
rs577479444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78823046 | CATTCCACACCCGCA[C/G]GCTACACTTCCCCTC | 57602 |
rs577602840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819042 | ACCAGGAAACTAAAT[A/G]AAATACAGGAAAAAG | 57602 |
rs577729539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78824551 | CCTGTCTCAAAAAGA[A/G]TGGTTTATGTACAAA | 57602 |
rs577729864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839921 | CCCAGCCAGCACCAT[C/T]TAGGCTCATTCCCGC | 57602 |
rs577731061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78833760 | TTTTAGAAACTGTGT[C/T]ATTTGGTAGTATTTT | 57602 |
rs577766930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78839391 | ATAAATAAAAGCATA[C/T]CAACTCCCGAAAAAT | 57602 |
rs577822359 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP36 | GRCh38.p7 | 17:78800459 | AACCCTTTCTGAACT[C/T]GTCCTCTGCCCAGCT | 57602 |
rs577883858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78805787 | TCACTCAAGCCTCTC[G/T]CCAAGGCCTCACTTC | 57602 |
rs578040935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP36 | GRCh38.p7 | 17:78819873 | CAACACTGTCAGGTG[A/C]GGGGACTTATTTCCC | 57602 |
rs578047670 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP36 | GRCh38.p7 | 17:78820206 | GCAGCCAGGAACAGC[A/G]GCTCACGCCTATAAT | 57602 |
rs578121408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP36 | GRCh38.p7 | 17:78789693 | TGGAACTTGATTGTA[C/T]CCAGCTGTCACCAAC | 57602 |
rs578150114 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP36 | GRCh38.p7 | 17:78815805 | ACATACATGCATACA[C/T]ACATCGTATACACAC | 57602 |
rs578165866 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78840763 | GCGGGCGCGCCACAA[C/G]CCTACGCAGCCCTGG | 57602 |
rs745409909 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | USP36 | GRCh38.p7 | 17:78806109 | CAAGCACACGCAACC[A/G]CAGGGAGAACCAGTT | 57602 |
rs745471043 | snp | C/T | 1.70563e-05 | 0.00292025 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803720 | TGGGAGGCGCGTCTC[C/T]GAGCCCAGCCTCTGC | 57602 |
rs745488086 | snp | A/G | 6.69098e-05 | 0.00578363 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836404 | AAACATAGAGCCATA[A/G]ATAACGAAATCCCGG | 57602 |
rs745500199 | snp | C/G/T | 3.29659e-05 | 0.00405981 | intron-variant | USP36 | GRCh38.p7 | 17:78813769 | GAGGGCGTGAGTTTA[C/G/T]TACCGCAGATAGAAC | 57602 |
rs745517175 | snp | C/G | 1.64811e-05 | 0.00287059 | intron-variant | USP36 | GRCh38.p7 | 17:78799034 | CAGAACTACCAGGCA[C/G]ACACGGGGGTCAGCA | 57602 |
rs745523486 | snp | C/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795688 | TTGCACCAAGATCTT[C/G]GCAACACGTGGGGCT | 57602 |
rs745557722 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820924 | GCCTTTACTGTTCTG[C/T]GGGTTCTGTTTCACC | 57602 |
rs745582308 | snp | C/T | 0.000530047 | 0.0162709 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813866 | TGGTACCACTGTCCA[C/T]TGCTTGCCTGAAGCA | 57602 |
rs745590990 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837293 | TATCCATTAGACACC[C/T]AAACTTAAACAAATG | 57602 |
rs745608145 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791291 | AGGCATGCACCACCA[C/T]GCCCGGCTGATTTTG | 57602 |
rs745624240 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78803318 | ATACCTACTTGGGGG[C/T]AGATTCTGTGGTTTT | 57602 |
rs745657752 | snp | A/G | 3.38937e-05 | 0.00411652 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803392 | GCCCTTACCTGTGCC[A/G]AAGTGGGTCCTGGTG | 57602 |
rs745673427 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836095 | GCCTCTCTGCCAGCA[C/T]ACTGCACATCTGTAC | 57602 |
rs745678922 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812875 | CTTTCCAGTCAGTGG[A/G]GAGGAAATAATCCCA | 57602 |
rs745699572 | in-del | -/TT | 1.65712e-05 | 0.00287843 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806959 | CCCCACACACCCACC[-/TT]TTCTTGGCAGAAAGG | 57602 |
rs745727493 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792172 | CAGAGAGTCAACACA[C/G]AGCAAAATGAATGTC | 57602 |
rs745801075 | in-del | -/TGAGAAAGATTAATGAATGATTGATTCGTGCTC | 1.65086e-05 | 0.00287298 | intron-variant | USP36 | GRCh38.p7 | 17:78818793 | CTATGAAGAAGGTGA[lengthTooLong]TGAGAAAGATTAATG | 57602 |
rs745838315 | snp | C/T | 2.13509e-05 | 0.00326726 | intron-variant | USP36 | GRCh38.p7 | 17:78807686 | AGCGAGAAGTCTCAG[C/T]TGGGCCACATCTTCT | 57602 |
rs745845475 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788525 | TTCTCCCAGCTGGTT[A/G]GTGGGGCAGTGGGGG | 57602 |
rs745904026 | snp | C/T | 0.000128626 | 0.0080185 | intron-variant | USP36 | GRCh38.p7 | 17:78827170 | CCGGGCTGGCTGTTG[C/T]CATAGGAATGTTCTG | 57602 |
rs745904699 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808238 | AGCATTTTTATGGGC[A/G]ATAACTCTCAATAAA | 57602 |
rs745914433 | snp | A/T | 1.65034e-05 | 0.00287253 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799683 | TTTTCTCCCGTAAGC[A/T]TTATCAGATGAGTAT | 57602 |
rs745954259 | snp | A/G | 2.49891e-05 | 0.00353467 | intron-variant | USP36 | GRCh38.p7 | 17:78827229 | GCCCTGGGAGGGTGG[A/G]TGGGGAAGCACGCAC | 57602 |
rs746001482 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797730 | TCCGATCTAGAGAAG[A/C]CTCAAAGCCTCTGTG | 57602 |
rs746035501 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807118 | GGTGGAACAGTTCGT[C/T]TCCTGAGAATCGCAG | 57602 |
rs746086023 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831837 | GTCTATAGTGCCAGC[A/T]ACTTGGGAGGCTAAG | 57602 |
rs746098543 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818228 | CAAGTCCCACCGCCC[A/G]GTGCTCATCACACTC | 57602 |
rs746120067 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807779 | TTTATCTGGACTCTT[C/G]GTAAAGACACTGTGG | 57602 |
rs746133689 | snp | C/T | 1.65326e-05 | 0.00287507 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807150 | GATGGGCCGCTCCAC[C/T]CCTGGGGGTCTGGGG | 57602 |
rs746209361 | snp | G/T | 1.66902e-05 | 0.00288874 | intron-variant | USP36 | GRCh38.p7 | 17:78814558 | AGCCTACATCCTGTT[G/T]GAAAAATCAAGGAAA | 57602 |
rs746215703 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823322 | TAGCTGCGTGTGATG[A/G]CGGCTACCAAAATCC | 57602 |
rs746232751 | snp | A/C | 1.65091e-05 | 0.00287303 | intron-variant | USP36 | GRCh38.p7 | 17:78820057 | ACACAGCAGAGGAAA[A/C]AGGCTGATTCAAGAA | 57602 |
rs746239853 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797430 | GGAAGCAGGGGAGGG[C/T]GGGCTCGGACACAAC | 57602 |
rs746280101 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822637 | CACTCTGAGCTCTGG[A/G]GCCTCTTCTCACCCG | 57602 |
rs746297185 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805202 | GGACCCCCGTCATCA[A/T]CTAAACAAACTATAA | 57602 |
rs746299341 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815330 | AGCGAGACTCCATCT[C/T]AAAACAATCAAAACA | 57602 |
rs746305768 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832520 | GAAGGGATGGCCATG[A/G]CTGCCTTACTCACAC | 57602 |
rs746329596 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816352 | TTTTTTAGGCCGGGC[A/G]TGATGGCTCACACCT | 57602 |
rs746370618 | snp | A/G | 1.65181e-05 | 0.00287381 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807451 | CACCTTCTTTCCAGG[A/G]TCGTCTAGGATGGTT | 57602 |
rs746376028 | snp | A/C | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787112 | TCCCGAGTAGCTGGG[A/C]TTACACGCACGCGCT | 57602 |
rs746379313 | snp | C/T | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814551 | TCCGGATAGCCTACA[C/T]CCTGTTTGAAAAATC | 57602 |
rs746432585 | snp | A/G | 1.65545e-05 | 0.00287697 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807492 | TGGGTGTCTGGGAGA[A/G]TTTGGGGGAAGGGGA | 57602 |
rs746446650 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817906 | GGCAACACAGCAAGA[A/T]GCTGTCTCTACAAAA | 57602 |
rs746488253 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828833 | AACATAGCGAGAACC[C/G]CATCTCTACAAAAAA | 57602 |
rs746494320 | snp | A/G | 2.15906e-05 | 0.00328555 | intron-variant | USP36 | GRCh38.p7 | 17:78802548 | CAGCTGCTTGGAAGT[A/G]AGAGGCAGCAGTCAG | 57602 |
rs746497209 | in-del | -/TTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78800972 | TGTTAGGGCAGTATT[-/TTT]TTTTTTTTTTTTTTT | 57602 |
rs746536596 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812615 | GAATGGCGGGAACCC[A/G]GGAGGCAGAGCTTGC | 57602 |
rs746556297 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837946 | AAAGAAAAGCCAGGT[A/G]CAGTGGCCTGGGCCT | 57602 |
rs746603194 | snp | C/T | 1.65012e-05 | 0.00287234 | splice-donor-variant, intron-variant | USP36 | GRCh38.p7 | 17:78799666 | GTCTCCAAATCAGTA[C/T]CTTTTCTCCCGTAAG | 57602 |
rs746611433 | snp | C/T | 4.95332e-05 | 0.00497636 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828908 | TTACTTTTCAGGTCT[C/T]GGATGAAGGAGACGG | 57602 |
rs746654233 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793247 | ATTCTTGAGGTAGCC[C/T]TGGAAGTCACTTACC | 57602 |
rs746670577 | in-del | -/AA | 3.17193e-05 | 0.00398229 | intron-variant | USP36 | GRCh38.p7 | 17:78820963 | TCGCTCTCCTACTGC[-/AA]AAGTGAAGGGCAGGA | 57602 |
rs746725250 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806186 | GGCCAAGTGGAGGCA[A/T]CGACGGGGTGAGAGG | 57602 |
rs746734943 | snp | A/G | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807420 | GGGAAAAGTGCTGTG[A/G]AGGAGCTGGCTTCTT | 57602 |
rs746737330 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830911 | TGGTGAACTCAAAAT[C/T]AGGCAAAAATTATGT | 57602 |
rs746746397 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799608 | TCCATTCCACACCCT[G/T]CCCTCCTACAAAACC | 57602 |
rs746792666 | snp | A/G | 1.65291e-05 | 0.00287476 | intron-variant | USP36 | GRCh38.p7 | 17:78798857 | CCCGGCTCTGAGCTG[A/G]GCCACGCCGCCCTGC | 57602 |
rs746835177 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836286 | AGAGGAGGCAAGAAG[C/G]TTCCCCAGTTCTCCA | 57602 |
rs746857462 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790019 | CAACAAATATTTACC[A/G]GGTGGCTGGTAAGTG | 57602 |
rs746876001 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801775 | ACTCAGGCTGGGAGT[A/T]CAGGGAGTCATTCCG | 57602 |
rs746907605 | snp | G/T | 1.64887e-05 | 0.00287125 | intron-variant | USP36 | GRCh38.p7 | 17:78820031 | AGGAGGACAAAAACA[G/T]GGAGTAAAATACACA | 57602 |
rs746938410 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810060 | CCATATTGGCAAGCT[G/T]GTCTCAAACTCCTGA | 57602 |
rs746938766 | snp | A/C/T | 6.59059e-05 | 0.00574014 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812891 | GAGGAAATAATCCCA[A/C/T]TGCCGATGTTCTTCT | 57602 |
rs746990181 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807128 | TTCGTTTCCTGAGAA[C/T]CGCAGAGATGGGCCG | 57602 |
rs747032450 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826390 | AAAATTAGCCAGGCA[C/T]GGTGGTAATCCCAGC | 57602 |
rs747063989 | snp | C/T | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807032 | TCAGTGGTGGTGTTG[C/T]TCAGGACAGGGGACT | 57602 |
rs747079506 | snp | A/G | 3.32127e-05 | 0.00407495 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807506 | AGTTTGGGGGAAGGG[A/G]ACCCCGAGGGCAGCT | 57602 |
rs747113355 | snp | A/G | 6.59446e-05 | 0.00574177 | intron-variant | USP36 | GRCh38.p7 | 17:78818650 | GAGCTGCCTGGGATG[A/G]TGTCACGAGCGCTCA | 57602 |
rs747176903 | snp | A/G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825717 | CTGACTGAAGCCCAG[A/G/T]GGTCAGTTTCTGTCC | 57602 |
rs747199387 | snp | A/G | 8.66889e-05 | 0.00658308 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803853 | TGAGGCAGCGCCGTC[A/G]AGATGGAGGAGCAGC | 57602 |
rs747200163 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78840889 | GTTCGCGCTGCGCTA[A/C]CTCCGAAAGGGTTGG | 57602 |
rs747265597 | snp | C/G | 5.27023e-05 | 0.00513307 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803898 | GTCCCTGGGGGCTTG[C/G]GGGTACTGGACAGCA | 57602 |
rs747270679 | snp | A/G | 1.68545e-05 | 0.00290292 | intron-variant | USP36 | GRCh38.p7 | 17:78814569 | TGTTTGAAAAATCAA[A/G]GAAAAGACAAATAAA | 57602 |
rs747340901 | snp | A/G | 3.987e-05 | 0.00446469 | intron-variant | USP36 | GRCh38.p7 | 17:78821086 | AACAGAGGCAGTGGA[A/G]CAGGTGGGGCCTGGC | 57602 |
rs747349917 | snp | G/T | 1.6869e-05 | 0.00290417 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803649 | TCCTCCGGGCGCTTC[G/T]TCTTCTTCCTCTTCC | 57602 |
rs747352765 | snp | C/T | 2.302e-05 | 0.00339256 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821016 | AGCGCGACGTCCAAG[C/T]AGGGGTCGTAGGTGT | 57602 |
rs747357961 | in-del | -/TTTTGCC | | | intron-variant | USP36 | GRCh38.p7 | 17:78814148 | CATCACCATGGCCGA[-/TTTTGCC]TTTTGCCAGGGTTCT | 57602 |
rs747364907 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831739 | CTGAGCCCAGGTGTT[G/T]GAGACCAGCCTGGGC | 57602 |
rs747404560 | snp | A/G | 1.65866e-05 | 0.00287976 | intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806315 | CATAAATAAAAACTT[A/G]GTGGTCTAAAAAAGG | 57602 |
rs747410231 | snp | C/G | 3.31378e-05 | 0.00407036 | intron-variant | USP36 | GRCh38.p7 | 17:78813038 | TAGGGAATTCTCTTA[C/G]TAGGCATTACAGAAA | 57602 |
rs747464539 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841966 | AACAAGATAACCATA[C/T]TAGTCTGATGCTGAG | 57602 |
rs747481265 | snp | A/C | 1.7386e-05 | 0.00294834 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807571 | CAGGGTGGAGCCATT[A/C]CTGGATATGGGCACA | 57602 |
rs747490867 | snp | A/G | 3.31686e-05 | 0.00407225 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835398 | GAGTCCTGCGCCCAC[A/G]CGGAAGACCCGCTCC | 57602 |
rs747526636 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796791 | TCCGGGAGGAAATGA[C/T]GGGGACAGACCCGAT | 57602 |
rs747537932 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822572 | CTTCGGGGTCAGGAG[C/T]CCTGCCCTCATTCAT | 57602 |
rs747607736 | snp | C/T | 0.000166387 | 0.00911952 | intron-variant | USP36 | GRCh38.p7 | 17:78806952 | GGCGAGACCCCCACA[C/T]ACCCACCTTCTTGGC | 57602 |
rs747662867 | snp | A/G | 3.29913e-05 | 0.00406135 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803536 | TGCCATCTTCCTGCC[A/G]TCTGACAGCGGGCAG | 57602 |
rs747750417 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793145 | AGCATTGAGAACCCT[A/G]AGGTAAGAAGGAGAA | 57602 |
rs747771918 | snp | A/C/T | 8.24782e-05 | 0.0064213 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803545 | CCTGCCGTCTGACAG[A/C/T]GGGCAGCTGTGCCTG | 57602 |
rs747793769 | snp | A/C | 1.83256e-05 | 0.00302696 | intron-variant | USP36 | GRCh38.p7 | 17:78835269 | CCCCACTGCTGCAAA[A/C]CCACACTCACAGCTG | 57602 |
rs747819654 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814433 | GTAGCAGTAATAGTG[C/T]CCGGCATGGCAGCTG | 57602 |
rs747847704 | snp | C/T | 2.03225e-05 | 0.00318761 | intron-variant | USP36 | GRCh38.p7 | 17:78827238 | GGGTGGGTGGGGAAG[C/T]ACGCACTTGGCACAG | 57602 |
rs747848786 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827685 | GGGTGGGAGGATCAC[C/T]TGAGCCCAGGAGTTC | 57602 |
rs747891305 | snp | C/T | 4.95233e-05 | 0.00497586 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806268 | GGTCATTGCCGGTCG[C/T]CCTCCACAGGGTGCT | 57602 |
rs747899194 | snp | G/T | 1.66269e-05 | 0.00288326 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836380 | GTGCATCACTGTGGG[G/T]ACAAGAAGAAACATA | 57602 |
rs747970888 | snp | A/G | 1.65222e-05 | 0.00287417 | intron-variant | USP36 | GRCh38.p7 | 17:78813014 | ATTCTGTCAAAGGAA[A/G]AAAACAAGTAGGGAA | 57602 |
rs747977802 | snp | A/G | 3.58738e-05 | 0.00423505 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827330 | CCTGGTTCCCAAAGC[A/G]GAAGTGTCGGGCGAT | 57602 |
rs748037192 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809991 | AGCTGGGATTACAGG[C/T]GCACGCCACCATGCC | 57602 |
rs748053436 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818399 | GCCCTGTCCTCCAGA[C/G]ATTCAAATTCACTGG | 57602 |
rs748129907 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789779 | CTTCAAATAGAGGAG[C/G]TAGTGCTCTAGTTCC | 57602 |
rs748146249 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833913 | TCCTCCTCTATTCTT[C/T]GGAAGAACGTGTAAA | 57602 |
rs748193135 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824664 | TAAATATGCTACCTA[C/T]AATTACTATAAAATA | 57602 |
rs748226097 | in-del | -/C | 9.89299e-05 | 0.00703244 | intron-variant | USP36 | GRCh38.p7 | 17:78798384 | TCACCCTTACACCCA[-/C]CCCCTCGGAACCGAC | 57602 |
rs748262294 | snp | A/G | 0.000250142 | 0.0111807 | intron-variant | USP36 | GRCh38.p7 | 17:78807645 | CTTGTCGCTAAGGAG[A/G]CCAAAGCAGAAAACA | 57602 |
rs748317095 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833409 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 57602 |
rs748383673 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78839750 | TAAACAACGCTCGCT[A/C]GCTCTCTGACGTGTA | 57602 |
rs748389961 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78799442 | CCCTGCCCCAACCCT[C/G]AGAAGCAGCTGTTCT | 57602 |
rs748391038 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78825631 | ACAGCCCCAAATCCA[A/C]ACCGTTATTCATTCT | 57602 |
rs748398837 | in-del | -/G | 0.000228215 | 0.0106797 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803778 | TCTCAGAGGGGCTCT[-/G]GGGGGGGCTCACTGG | 57602 |
rs748419616 | snp | C/G | 1.78369e-05 | 0.00298633 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807587 | CTGGATATGGGCACA[C/G]CAATCTCTTCAGTGG | 57602 |
rs748436801 | in-del | -/TT | | | intron-variant | USP36 | GRCh38.p7 | 17:78794097 | CTGTCATCTCACCTC[-/TT]GAGTCCATCTCCTAA | 57602 |
rs748484424 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78829558 | CAAATCCTTTCCTAT[A/C]TGAGGGCTATACAGT | 57602 |
rs748505360 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795854 | CTCCCTCCAGCTCCA[C/T]TCCCAAGCACAAAAT | 57602 |
rs748512116 | snp | A/G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796779 | ACCTGCGACGACTCC[A/G/T]GGAGGAAATGACGGG | 57602 |
rs748543305 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78831038 | AGACCATCCTGGCTT[-/A]ACACAGTGAAACCCC | 57602 |
rs748545756 | snp | A/G | 3.34638e-05 | 0.00409033 | intron-variant | USP36 | GRCh38.p7 | 17:78813878 | CCATTGCTTGCCTGA[A/G]GCAGCCAAGGATGTT | 57602 |
rs748548914 | snp | C/T | 1.71085e-05 | 0.00292471 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803655 | GGGCGCTTCTTCTTC[C/T]TCCTCTTCCTCTTCC | 57602 |
rs748601527 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807059 | GACTTCAGCTTCACC[A/G]TCTTAGAATCTGCTC | 57602 |
rs748682998 | snp | A/C/T | 3.30498e-05 | 0.00406497 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836068 | CATCCACTTCGTCAC[A/C/T]CCGGAGTGAGGGCCT | 57602 |
rs748686578 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790093 | TGGCAGAATAATACC[-/T]TTTTTTTTTTTTTGA | 57602 |
rs748713371 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821994 | TAGTAGCCTGCGTTT[C/G]ACGATCCAACCTGAA | 57602 |
rs748767284 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802587 | AAATTGGAAGGGGAG[C/G]AGGAGCGCACAGACA | 57602 |
rs748807822 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822520 | ATCTCCCCGGCTCTG[C/T]ACCCGTCTCAGAGAG | 57602 |
rs748811896 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798942 | TCGTCCCAGTCATCA[A/G]CCACGGTCTCAGTCC | 57602 |
rs748819593 | snp | C/G | 1.66724e-05 | 0.0028872 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836396 | ACAAGAAGAAACATA[C/G]AGCCATAGATAACGA | 57602 |
rs748850563 | snp | C/G | 1.66418e-05 | 0.00288455 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807196 | GCTGCTGGCCGAGTG[C/G]TCTGGGCTGGAGCTG | 57602 |
rs748888707 | snp | A/C | 1.66668e-05 | 0.00288672 | intron-variant | USP36 | GRCh38.p7 | 17:78806949 | AGCGGCGAGACCCCC[A/C]CACACCCACCTTCTT | 57602 |
rs748890796 | snp | A/G | 4.94939e-05 | 0.00497439 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803544 | TCCTGCCGTCTGACA[A/G]CGGGCAGCTGTGCCT | 57602 |
rs748962197 | snp | C/T | 3.30071e-05 | 0.00406232 | intron-variant | USP36 | GRCh38.p7 | 17:78798875 | CACGCCGCCCTGCTC[C/T]CTCAAGCCTGTGGTC | 57602 |
rs748975875 | snp | A/C | 1.6528e-05 | 0.00287467 | intron-variant | USP36 | GRCh38.p7 | 17:78813020 | TCAAAGGAAGAAAAC[A/C]AGTAGGGAATTCTCT | 57602 |
rs749013403 | snp | C/T | 1.68975e-05 | 0.00290662 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803645 | TGTGTCCTCCGGGCG[C/T]TTCTTCTTCTTCCTC | 57602 |
rs749064428 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834544 | CTCCACCTTCTGGGT[C/T]CAAGCAATTCTCCTG | 57602 |
rs749070609 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818306 | CAGAAGCTGCGGTAA[A/G]TCCATTAAGACAGTG | 57602 |
rs749093610 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836042 | CCTACTAATTAGTCA[A/G]TATTTAAGTCCATCC | 57602 |
rs749135681 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818750 | TGTGGATGGTGAAGC[A/G]CTTGCTGGCTGGAAC | 57602 |
rs749169554 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78818882 | ACTGCTCTGTAATAG[C/T]GGAATCTTCATCAAT | 57602 |
rs749178629 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842467 | GCTGGGTATGGTGGC[A/G]CACGCCTGTAATCCG | 57602 |
rs749211945 | in-del | -/GCATCCT | 1.64727e-05 | 0.00286986 | frameshift-variant, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798981 | CTGCTGTCTTCAATA[-/GCATCCT]GACTGACCGCCGACA | 57602 |
rs749227575 | snp | C/T | 4.94287e-05 | 0.00497111 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818679 | CACCTTGGTGATCTT[C/T]CCCCCGCTGAAGTTG | 57602 |
rs749228894 | snp | A/G | 1.85654e-05 | 0.0030467 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827340 | AAAGCGGAAGTGTCG[A/G]GCGATCTCTAAAAGA | 57602 |
rs749232089 | in-del | -/GGTTTTCATGGGGTGGGTGAGG | 1.64795e-05 | 0.00287045 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806200 | AACGACGGGGTGAGA[-/GGTTTTCATGGGGTGGGTGAGG]TCGGAGGATGGTGAG | 57602 |
rs749232173 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792307 | GACAGGGTAATTAAT[A/G]GAGCAAGGTCCCCAG | 57602 |
rs749240080 | in-del | -/GATAACTCTCAATAAATAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78808238 | AGCATTTTTATGGGC[-/GATAACTCTCAATAAATAT]CTTTAAGACAGAGCC | 57602 |
rs749241898 | snp | C/T | 2.13691e-05 | 0.00326865 | intron-variant | USP36 | GRCh38.p7 | 17:78804022 | GGATGTTCTGAAAGA[C/T]CCAGCAGAGCTGTTC | 57602 |
rs749274687 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836078 | GTCACCCCGGAGTGA[A/G]GGCCTCTCTGCCAGC | 57602 |
rs749288943 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798725 | CCCCCTATTGACAAA[C/G]GGGCGGAAGCTGCGA | 57602 |
rs749294584 | snp | A/G | 4.94629e-05 | 0.00497283 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807103 | TTTGGAGTGGCCAGC[A/G]GTGGAACAGTTCGTT | 57602 |
rs749322043 | in-del | -/AGTC | 1.65081e-05 | 0.00287293 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814475 | ACCAGGACAGCATAG[-/AGTC]AGTCCATACATGACA | 57602 |
rs749326552 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832586 | ACCTGTGCCAGGTTA[C/T]GGGGATTTACAGATA | 57602 |
rs749329841 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | USP36 | GRCh38.p7 | 17:78822017 | AACCTGAAAAGGAGA[C/T]CCCAGCCTTTAAGGG | 57602 |
rs749336576 | snp | A/C/T | 3.41829e-05 | 0.00413407 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803735 | TGAGCCCAGCCTCTG[A/C/T]GGCTCTCCCACAAAG | 57602 |
rs749381823 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788497 | CAAGTAATTCTATTT[C/T]GTTACCTTTATGTTC | 57602 |
rs749397640 | snp | G/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807113 | CCAGCGGTGGAACAG[G/T]TCGTTTCCTGAGAAT | 57602 |
rs749475768 | snp | C/T | 1.81319e-05 | 0.00301091 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802501 | TTGGAGACTCTTCCA[C/T]GGCCTCTGGATCACC | 57602 |
rs749494025 | snp | A/G | 1.65067e-05 | 0.00287282 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835497 | CTCATACGTGTGCTC[A/G]CTGCCTGAGGAAGAA | 57602 |
rs749520497 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78795010 | GAGACTCTGTTCGGG[-/A]AAAAAAAAAAAAAAA | 57602 |
rs749527891 | snp | A/G | 1.64751e-05 | 0.00287007 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798418 | CTTCCACAGGGGCAC[A/G]GTCAGCGGCGATAGC | 57602 |
rs749528042 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833292 | TGTTCTTTTTTTTAT[C/G]TTTTTTTGAGACGGA | 57602 |
rs749536109 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809126 | TTGAATGAGATCTTT[C/T]GTTTACAAATGTTAA | 57602 |
rs749592446 | snp | G/T | 1.65737e-05 | 0.00287864 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799766 | GAGGGGCCTGGCTCA[G/T]CCCTGCAATCGGAGC | 57602 |
rs749616993 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78838085 | TGGGCAACATCGTGA[A/G]ACCCCATCTTTAAAA | 57602 |
rs749674542 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78806746 | ACATGAGCATCACCA[C/G]ATCAGGGCTCTCTCA | 57602 |
rs749682193 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78816141 | TGTGTTTAGGAACTC[A/C]GAAAAACATACGCAT | 57602 |
rs749704387 | snp | C/T | 1.65105e-05 | 0.00287315 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807434 | GGAGGAGCTGGCTTC[C/T]TCACCTTCTTTCCAG | 57602 |
rs749726358 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78793656 | CACGTCCTTGGCGTA[-/C]CCACATCCTCATTGC | 57602 |
rs749736539 | snp | A/G | 1.71546e-05 | 0.00292865 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803782 | CAGAGGGGCTCTGGG[A/G]GGGCTCACTGGCCTC | 57602 |
rs749785145 | snp | C/T | 1.85951e-05 | 0.00304913 | intron-variant | USP36 | GRCh38.p7 | 17:78827156 | TGGGTAGAAAGGTGC[C/T]GGGCTGGCTGTTGCC | 57602 |
rs749810792 | snp | C/T | 1.77584e-05 | 0.00297974 | intron-variant | USP36 | GRCh38.p7 | 17:78813914 | AAACAAAACAATCAA[C/T]AAGCATCCCATTATC | 57602 |
rs749824079 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815464 | CTTTGTCAAGCATCT[C/G]CATTAGTTCTCTCAC | 57602 |
rs749855773 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807964 | CTGCCTCAGCCTCCA[C/G]AAGTGTTGGGATTAC | 57602 |
rs749863780 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814436 | GCAGTAATAGTGCCC[A/G]GCATGGCAGCTGTAG | 57602 |
rs749894320 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802652 | TGTGACCCAGTGCAC[A/G]CAGGTCCCTGCAACA | 57602 |
rs749907051 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796705 | GACAGCAGGATGCCT[A/C]TGGCCCAGCAGAGCC | 57602 |
rs749925025 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841653 | ATTCCCTTGGGCAGG[C/T]TGAGAGTGTTGGTTC | 57602 |
rs749941825 | snp | G/T | 1.65086e-05 | 0.00287298 | intron-variant | USP36 | GRCh38.p7 | 17:78799650 | GGCAAACAGAAGTCC[G/T]GTCTCCAAATCAGTA | 57602 |
rs749992952 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797432 | AAGCAGGGGAGGGCG[C/G]GCTCGGACACAACGG | 57602 |
rs750051333 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817316 | GACACCTGAGTCTAC[A/G]ACATTAAGAATCTGC | 57602 |
rs750067239 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831119 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGCCAGG | 57602 |
rs750077139 | snp | G/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821987 | ACCAAGGTAGTAGCC[G/T]GCGTTTGACGATCCA | 57602 |
rs750083762 | snp | A/C | 0.000162853 | 0.0090222 | intron-variant | USP36 | GRCh38.p7 | 17:78827091 | CTATTTGGGCTCCAA[A/C]AGTTTGAGTACCCAG | 57602 |
rs750088774 | snp | C/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836137 | GCCGGTGGGTCATCT[C/T]CACTCTTGTGGCGAC | 57602 |
rs750095438 | snp | A/G | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807482 | GGCATGTGTGTGGGT[A/G]TCTGGGAGAGTTTGG | 57602 |
rs750180001 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814272 | TTCACTCCACGCAGA[C/G]AGGCAACAACGAGGA | 57602 |
rs750200488 | snp | C/T | 3.29984e-05 | 0.00406179 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806256 | GAGGTGGACGGAGGT[C/T]ATTGCCGGTCGCCCT | 57602 |
rs750218570 | snp | A/G | 1.65141e-05 | 0.00287346 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835329 | GGCTAGAGGTGGTGT[A/G]TAGGTCAAGCACTGG | 57602 |
rs750276583 | snp | C/T | 3.29571e-05 | 0.00405924 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78820004 | AGCACGCACAATATT[C/T]GCAGCTTGCTGAGGA | 57602 |
rs750304765 | snp | A/G | 1.65067e-05 | 0.00287282 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807408 | GAGCAGTTCTGGGGG[A/G]AAAGTGCTGTGGAGG | 57602 |
rs750323417 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78830553 | CCAAAGGGCAAGCAC[A/G]CCTTCAAATCTGCTA | 57602 |
rs750329115 | in-del | -/C | 2.19986e-05 | 0.00331644 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835460 | GCACTTTCTGCGGGG[-/C]TGGGACTCCGTCACC | 57602 |
rs750372584 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78813072 | AGAGAATTAGAATAA[A/G]TTAAGGCGGGGCAAA | 57602 |
rs750423140 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836025 | CACATTCTCTTGTTT[C/T]TCCTACTAATTAGTC | 57602 |
rs750424380 | snp | C/G | 2.16279e-05 | 0.00328839 | intron-variant | USP36 | GRCh38.p7 | 17:78835231 | AGTGCATGGGCTTAT[C/G]TAATCCAGAGGACCC | 57602 |
rs750429522 | snp | G/T | 1.65285e-05 | 0.00287471 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807466 | GTCGTCTAGGATGGT[G/T]GGCATGTGTGTGGGT | 57602 |
rs750429683 | snp | C/T | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806223 | TGGGGTGGGTGAGGT[C/T]GGAGGATGGTGAGGG | 57602 |
rs750457985 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836268 | TAAAAGGACCTTCTT[A/G]GCAGAGGAGGCAAGA | 57602 |
rs750482825 | snp | C/T | 1.65655e-05 | 0.00287793 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807171 | GGGTCTGGGGGGCCT[C/T]GGTGGAGTCGCTGCT | 57602 |
rs750506724 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836363 | TATCCACTATTGGCA[C/T]GGTGCATCACTGTGG | 57602 |
rs750510070 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828169 | CAGCGAGCTGTGATT[C/G]CACCACTGTCCTCCA | 57602 |
rs750538817 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837243 | TTTAAAAGTGAGGAA[A/G]GAGAAGAAAAGCAAG | 57602 |
rs750573740 | snp | A/T | 4.94605e-05 | 0.0049727 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803493 | TCCGTAACACATCCC[A/T]CCTGCTGGCCATTCA | 57602 |
rs750574485 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809078 | CCACTTTAACATTCA[C/T]ATTCTCTGCACATGC | 57602 |
rs750605688 | snp | A/G | 9.88435e-05 | 0.00702937 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812930 | TCTGGAATCACACTC[A/G]GGCGGCCGGGAAGGG | 57602 |
rs750608579 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792786 | TGCAGTGGCATGATC[C/T]TGGCTCACTGCAACC | 57602 |
rs750615979 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819828 | AAGAAATGCGAGCAG[C/T]GGTCACCGCTAAGGA | 57602 |
rs750620819 | snp | C/T | 3.32127e-05 | 0.00407495 | intron-variant | USP36 | GRCh38.p7 | 17:78798589 | CACAGTTCCCAAAAA[C/T]GGCTCTTTCCTGGCC | 57602 |
rs750640936 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805615 | GAGGCACCTAAGAGA[C/T]GCAGGCAGCCCCTGC | 57602 |
rs750674479 | snp | C/T | 1.65732e-05 | 0.00287859 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803607 | TGTCTCTGTGTCTGC[C/T]CCTCCTGCAGGGCGC | 57602 |
rs750704070 | snp | C/T | 3.56481e-05 | 0.0042217 | intron-variant | USP36 | GRCh38.p7 | 17:78829012 | TCCCTGGTGGCCTGC[C/T]GGCGTGGAAGGAGGA | 57602 |
rs750783345 | snp | A/G | 1.72234e-05 | 0.00293452 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807563 | TTCAGGCCCAGGGTG[A/G]AGCCATTCCTGGATA | 57602 |
rs750823481 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818723 | GGGAAAGGGTTAAGA[C/T]GTTGGATGTTCTGTG | 57602 |
rs750829364 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789559 | CAAGAGGCTGCAAAG[C/T]GAACTGCTCACACAG | 57602 |
rs750848663 | snp | C/T | 6.66756e-05 | 0.0057735 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807221 | GAGCTGCTGGAGCCC[C/T]TCCTGTCGAGGCCAG | 57602 |
rs750876928 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825401 | AGAAGCTCACCATTG[A/G]TGTCATTCTTATTTT | 57602 |
rs750890843 | snp | C/T | 1.75502e-05 | 0.00296223 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803895 | GACGTCCCTGGGGGC[C/T]TGGGGGTACTGGACA | 57602 |
rs750901899 | snp | C/G | 1.85768e-05 | 0.00304763 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803952 | GGTTGCAGGCGGCTG[C/G]ATGATTGGGGAGCAG | 57602 |
rs750917241 | snp | A/G | 1.69263e-05 | 0.0029091 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827289 | CATGGCGTCGATGGT[A/G]TACCGCAGGAACTCA | 57602 |
rs750931172 | snp | C/T | 3.41945e-05 | 0.00413474 | intron-variant | USP36 | GRCh38.p7 | 17:78802302 | CACCCATGCGGTTCC[C/T]ACCCCCTCGCCCGGT | 57602 |
rs750932341 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787484 | AATACAGAACCATTT[C/G]TAATCAAAATCAATG | 57602 |
rs750939157 | snp | A/G/T | 4.94713e-05 | 0.00497329 | intron-variant | USP36 | GRCh38.p7 | 17:78818644 | CCCACGGAGCTGCCT[A/G/T]GGATGGTGTCACGAG | 57602 |
rs750968415 | snp | G/T | 0.000340824 | 0.0130498 | intron-variant | USP36 | GRCh38.p7 | 17:78827366 | AAAGAGGAAGAAACA[G/T]GGAGGGAAGAGCTCG | 57602 |
rs750978736 | in-del | -/CGTCCGT | 1.64901e-05 | 0.00287137 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803476 | TGCTCGCGTGGTGGC[-/CGTCCGT]AACACATCCCACCTG | 57602 |
rs750993632 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816437 | TCAAGACCAGCCTGG[C/G]CAACATGGTGGAACC | 57602 |
rs751006041 | snp | C/T | 1.65359e-05 | 0.00287536 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807475 | GATGGTTGGCATGTG[C/T]GTGGGTGTCTGGGAG | 57602 |
rs751034921 | snp | C/T | 1.96103e-05 | 0.00313126 | intron-variant | USP36 | GRCh38.p7 | 17:78835260 | CCACAGCCACCCCAC[C/T]GCTGCAAACCCACAC | 57602 |
rs751076196 | snp | A/T | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795583 | CCAGGACAGGTGGAA[A/T]CAGCGAGACTGTGGT | 57602 |
rs751171331 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78803074 | CTCCTGAGTAGCTGG[G/T]ACTATAGGTGCATGC | 57602 |
rs751174118 | snp | A/G | 3.4943e-05 | 0.00417975 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803883 | CTCCGTGGTTCTGAC[A/G]TCCCTGGGGGCTTGG | 57602 |
rs751186255 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839885 | AGCACAGGCCTCATC[C/T]ACATTTCCACCTGCG | 57602 |
rs751203905 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790545 | ATCTGTCTGCCGTGG[C/G]CTCCCAAAGAGCTGG | 57602 |
rs751245238 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838792 | GTGGAGGCGACTCTT[-/C]CTGTGCCTTCTCTTC | 57602 |
rs751300774 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792116 | AGAGTGGGAATTAGG[-/T]CACTGAGAAGTGATG | 57602 |
rs751342755 | snp | C/T | 3.32629e-05 | 0.00407803 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803622 | CCCTCCTGCAGGGCG[C/T]TGGCAGCTGTGTCCT | 57602 |
rs751368117 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812698 | CGAGACTCTGTCTCG[A/G]AAAAAAAAAAAAAAA | 57602 |
rs751395789 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798925 | TCCCTCGGTCAAACT[C/T]TTCGTCCCAGTCATC | 57602 |
rs751426689 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830040 | CATCGAGCCCAGCCC[C/T]GACAGTGGTACATTT | 57602 |
rs751433991 | snp | A/C | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812986 | GCCCTCGGGACTTTT[A/C]TTAGAGCCTGGAATT | 57602 |
rs751441640 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841582 | GAGCACGTATTTCTT[C/T]TGCAGTATTTTTAAA | 57602 |
rs751483793 | snp | A/G | 1.65154e-05 | 0.00287358 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835362 | GGTGGCATTGAGAAA[A/G]CAGGTGTTGCCAAGG | 57602 |
rs751504294 | snp | G/T | 3.29794e-05 | 0.00406061 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803521 | TCACCTGTGGCTGTG[G/T]GCCATCTTCCTGCCG | 57602 |
rs751538757 | snp | C/T | 1.7465e-05 | 0.00295503 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835434 | CAGAGACAGTCGCTC[C/T]GTGGGGAAAAGCACT | 57602 |
rs751545333 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794139 | GACCTCACTTCTAGC[C/T]TATGCTACTAATGCC | 57602 |
rs751555738 | snp | C/T | 2.52765e-05 | 0.00355494 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78820992 | GGACAGATCTGTACC[C/T]GGATCTCCAGCGCGA | 57602 |
rs751636964 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791946 | ATCCTGACAGAGGGT[A/G]GATCGGTCGGCTGTT | 57602 |
rs751661704 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835585 | GAAACTCCTGAAGCA[C/T]ACACTTAGCATGCAG | 57602 |
rs751667887 | snp | C/T | 1.91291e-05 | 0.0030926 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803974 | GGGGAGCAGGTGACA[C/T]AGCCCTGTGGGGACA | 57602 |
rs751668235 | snp | A/G | 2.24636e-05 | 0.00335131 | intron-variant | USP36 | GRCh38.p7 | 17:78827375 | GAAACAGGGAGGGAA[A/G]AGCTCGTGTCTTCTC | 57602 |
rs751671826 | snp | C/T | 4.99405e-05 | 0.00499677 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807273 | GCCCATGCCCGTTGG[C/T]AGTGGCTGTAGCCAG | 57602 |
rs751675560 | snp | A/G | 1.65059e-05 | 0.00287275 | intron-variant | USP36 | GRCh38.p7 | 17:78813739 | AAAAGAGCAGAGGGA[A/G]TGAGCTCATCTGGGG | 57602 |
rs751681966 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787718 | ACCTTTCCATACTGT[C/T]ATGGGTTGAGTCATG | 57602 |
rs751684056 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811302 | GTAACTTAGAGGGTA[C/G]TTCCTAATGGTTAAC | 57602 |
rs751724223 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818000 | TAAGGCAGGGGGATC[A/G]CTTGAGCTTGGGAGG | 57602 |
rs751727033 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792730 | TTTTTTTGTTGTCGT[C/T]GTTTTTGAGACAGAG | 57602 |
rs751728424 | snp | A/T | 1.65811e-05 | 0.00287929 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836369 | CTATTGGCATGGTGC[A/T]TCACTGTGGGGACAA | 57602 |
rs751749596 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834602 | CAGGTGCACCCCATC[A/G]CGCCTAATTTTTATA | 57602 |
rs751829662 | snp | A/G | 1.70714e-05 | 0.00292154 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827308 | CGCAGGAACTCATGC[A/G]CGTCCTCCTGGTTCC | 57602 |
rs751840907 | snp | A/C | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807049 | CAGGACAGGGGACTT[A/C]AGCTTCACCGTCTTA | 57602 |
rs751864035 | snp | C/T | 0.000214262 | 0.0103482 | intron-variant | USP36 | GRCh38.p7 | 17:78798396 | CCACCCCCTCGGAAC[C/T]GACCTCCTTCCACAG | 57602 |
rs751878644 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808871 | CTTAAAAAATATTTG[A/T]TGAGCTTTTCCTGTA | 57602 |
rs751879652 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809605 | CACTCTGCCCATGGA[A/G]TTCCTGTGGCAAGTG | 57602 |
rs751898095 | snp | A/G | 1.66827e-05 | 0.00288809 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807229 | GGAGCCCCTCCTGTC[A/G]AGGCCAGCGCTCTCG | 57602 |
rs751922478 | snp | C/G | 1.66043e-05 | 0.00288129 | intron-variant | USP36 | GRCh38.p7 | 17:78812830 | AGCACCAAGACCAGC[C/G]ACTTTGGCCTCCATC | 57602 |
rs751922768 | in-del | -/TCTTCC | 6.76888e-05 | 0.0058172 | cds-indel, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803653 | CCGGGCGCTTCTTCT[-/TCTTCC]TCTTCCTCTTCCCGT | 57602 |
rs752003990 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798462 | CTTTGCTGGGTGAGT[A/C]ACAGACCAGAAGTTC | 57602 |
rs752023189 | snp | C/G | 1.89914e-05 | 0.00308145 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802450 | CTTCTACTGCCCGCT[C/G]TGTCTCCTGCTTTCT | 57602 |
rs752027387 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832477 | GCCCATGGGACCGGT[A/G]TTGGAAGGAAGACCA | 57602 |
rs752073922 | snp | C/T | 0.00011533 | 0.00759287 | intron-variant | USP36 | GRCh38.p7 | 17:78806145 | CCAGAAGATCCCGGC[C/T]CAAAGCTTACCTGGC | 57602 |
rs752082089 | in-del | -/AAT | 1.64795e-05 | 0.00287045 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812881 | AGTCAGTGGGGAGGA[-/AAT]AATCCCATTGCCGAT | 57602 |
rs752124840 | snp | C/G | 3.30371e-05 | 0.00406417 | intron-variant | USP36 | GRCh38.p7 | 17:78818797 | TGAAGAAGGTGATGA[C/G]AAAGATTAATGAATG | 57602 |
rs752152272 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817089 | ACTGTACCTTCTCTA[C/T]GTTTAGATACACAAA | 57602 |
rs752320546 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833016 | AGCCAGGCGTGGTGG[C/T]GGGCACCTGCAGTCC | 57602 |
rs752331748 | in-del | -/GACA | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836798 | GGTTATACACACACG[-/GACA]CACACACACACACAC | 57602 |
rs752343637 | snp | A/G | 1.65493e-05 | 0.00287652 | stop-gained, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807486 | TGTGTGTGGGTGTCT[A/G]GGAGAGTTTGGGGGA | 57602 |
rs752387600 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788142 | AAGTTGTGTTTAAAA[C/T]TGCATATGCATAGGT | 57602 |
rs752431621 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825221 | GGAAACATTCACAAA[C/T]GCTGGTCACCTATAA | 57602 |
rs752462664 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813819 | TCAGAACCACCTTGA[C/T]GTTGCTGGAATGGAC | 57602 |
rs752465801 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839651 | ACTCCTTAATGTAGA[C/T]GCAGAGATTTTGAAC | 57602 |
rs752471102 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796298 | GCAAGTCAACACCCC[A/G]AGAAGAAAAGGAACA | 57602 |
rs752525450 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | USP36 | GRCh38.p7 | 17:78799071 | CAGGTTCCCAGGTCC[C/G]CTGTGGCTTCACTTC | 57602 |
rs752528272 | snp | C/T | 1.67542e-05 | 0.00289427 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803636 | GCTGGCAGCTGTGTC[C/T]TCCGGGCGCTTCTTC | 57602 |
rs752625653 | in-del | -/TTCTTTTTTTTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78791127 | ATTCCCAATCTGGCC[-/TTCTTTTTTTTTT]TTTTTTTTTTTTTAG | 57602 |
rs752631032 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807031 | CTCAGTGGTGGTGTT[G/T]CTCAGGACAGGGGAC | 57602 |
rs752637504 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798931 | GGTCAAACTCTTCGT[C/T]CCAGTCATCAACCAC | 57602 |
rs752717080 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797752 | GCCTCTGTGTTGGGC[A/G]GTCTGTGGACACTGG | 57602 |
rs752781481 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801279 | CCACCCCCGGCCAGG[G/T]CAGTACTTCTGAGAG | 57602 |
rs752801618 | snp | C/T | 1.82134e-05 | 0.00301768 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802482 | TTTTTCTTTTTCTTT[C/T]TCCTTGGAGACTCTT | 57602 |
rs752841410 | snp | C/T | 3.31082e-05 | 0.00406854 | intron-variant | USP36 | GRCh38.p7 | 17:78818814 | AAGATTAATGAATGA[C/T]TGATTCGTGCTCTGA | 57602 |
rs752847968 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78826255 | TTTTCTTAAGCCAGG[A/C]ATGGTGGCTCATGCC | 57602 |
rs752849076 | snp | C/T | 2.66642e-05 | 0.00365122 | intron-variant | USP36 | GRCh38.p7 | 17:78827397 | TGTCTTCTCATCAAA[C/T]GGCCTGCGGCTGCTT | 57602 |
rs752877841 | in-del | -/GGA | 1.64738e-05 | 0.00286995 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812944 | CGGGCGGCCGGGAAG[-/GGA]GGAGGAGCCTGTCCT | 57602 |
rs752888548 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807028 | AGGCTCAGTGGTGGT[A/G]TTGCTCAGGACAGGG | 57602 |
rs752900278 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818747 | TTCTGTGGATGGTGA[A/G]GCGCTTGCTGGCTGG | 57602 |
rs752984122 | snp | C/G | 1.71507e-05 | 0.00292832 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803780 | CTCAGAGGGGCTCTG[C/G]GGGGGCTCACTGGCC | 57602 |
rs752986292 | snp | A/G | 0.0021479 | 0.0327007 | intron-variant | USP36 | GRCh38.p7 | 17:78827123 | GGCAAATTCTGCCAC[A/G]TCTACCCAAGGGCAG | 57602 |
rs753000711 | snp | A/T | 1.64991e-05 | 0.00287215 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828935 | ACGGGCTTGATGGCG[A/T]TGCCGCTGTTGGCGA | 57602 |
rs753024030 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817497 | CGGTGGCTCATGCCT[A/G]TTATCCCAGCACTTT | 57602 |
rs753032774 | snp | A/T | 1.64757e-05 | 0.00287012 | intron-variant | USP36 | GRCh38.p7 | 17:78806152 | ATCCCGGCCCAAAGC[A/T]TACCTGGCTCTATGG | 57602 |
rs753068501 | in-del | -/AGCCATTCAGGCAG | 1.82647e-05 | 0.00302192 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827252 | GCACGCACTTGGCAC[-/AGCCATTCAGGCAG]GCTTTCTGCATGGCG | 57602 |
rs753074196 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819964 | TCTCTCCACTCAGGA[C/T]ATCTGCTTTCACAAA | 57602 |
rs753111998 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808049 | ATAAAACCAGTACAT[C/T]TTCATCAAGATTTGG | 57602 |
rs753131945 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836237 | TCTTGCTGGCTGGCT[C/T]GAACTCGATTTTCTG | 57602 |
rs753146805 | snp | A/T | 1.65638e-05 | 0.00287778 | intron-variant | USP36 | GRCh38.p7 | 17:78812840 | CCAGCCACTTTGGCC[A/T]CCATCATTCTCACAA | 57602 |
rs753159695 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798481 | GACCAGAAGTTCCGT[C/T]GAGTCTGAAGTTTCT | 57602 |
rs753192647 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836146 | TCATCTCCACTCTTG[C/T]GGCGACTAGCTCCCT | 57602 |
rs753209387 | snp | C/T | 1.64806e-05 | 0.00287054 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798402 | CCTCGGAACCGACCT[C/T]CTTCCACAGGGGCAC | 57602 |
rs753214330 | snp | A/G | 1.76918e-05 | 0.00297415 | intron-variant | USP36 | GRCh38.p7 | 17:78803359 | TCGTCAGAGGTAGAC[A/G]GATGCCACTTTGCTC | 57602 |
rs753237355 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78798309 | AGCCCACATACATCA[A/T]ACACACACGCCACAC | 57602 |
rs753273372 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812917 | CTTCTTGGAGTGATC[C/T]GGAATCACACTCGGG | 57602 |
rs753323366 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821966 | TACCCTCCAAAAATT[C/T]GATGGACCAAGGTAG | 57602 |
rs753329297 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787803 | TTATTTGGAAGTGGG[G/T]TCTTTGCAGATGTAA | 57602 |
rs753373680 | snp | G/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807089 | CCACTTGGCGGCGTT[G/T]TGGAGTGGCCAGCGG | 57602 |
rs753398022 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797860 | CAGCTCCCGGGAAGG[A/G]ACGCCTTGTCTCCAG | 57602 |
rs753470827 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823866 | GCAGACAGAGGAGGC[A/G]CTCTGGATACGAATC | 57602 |
rs753487043 | snp | A/T | 1.65296e-05 | 0.00287481 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836060 | TTTAAGTCCATCCAC[A/T]TCGTCACCCCGGAGT | 57602 |
rs753508915 | snp | C/T | 4.94588e-05 | 0.00497262 | intron-variant | USP36 | GRCh38.p7 | 17:78798390 | TTACACCCACCCCCT[C/T]GGAACCGACCTCCTT | 57602 |
rs753528093 | snp | C/G | 2.36376e-05 | 0.00343777 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835466 | TCTGCGGGGCTGGGA[C/G]TCCGTCACCACAGCT | 57602 |
rs753594226 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819750 | TAGCTATAAAAATCA[-/T]TAGCTATTGCTTCAT | 57602 |
rs753599299 | snp | C/G | 3.30142e-05 | 0.00406276 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807403 | CCCCTGAGCAGTTCT[C/G]GGGGAAAAGTGCTGT | 57602 |
rs753610612 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807041 | GTGTTGCTCAGGACA[A/G]GGGACTTCAGCTTCA | 57602 |
rs753630462 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810328 | GGTCTTGCTCTGTTG[C/T]CCAGGCTGGTGTGGA | 57602 |
rs753633728 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837356 | AAAAGCCAAGCAGGA[C/G]AGTGGGGAGATCACA | 57602 |
rs753682531 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799002 | TGACTGACCGCCGAC[A/G]TCTTGCCATCCCAGG | 57602 |
rs753693385 | snp | A/G | 8.25239e-05 | 0.00642302 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828949 | GTTGCCGCTGTTGGC[A/G]AAGGCCTGGACAATG | 57602 |
rs753702596 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819850 | CGCTAAGGAAGAGTG[G/T]GTGGGCACAACACTG | 57602 |
rs753706546 | snp | A/C | 4.96085e-05 | 0.00498014 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813859 | ATTCATCTGGTACCA[A/C]TGTCCATTGCTTGCC | 57602 |
rs753790028 | snp | A/G | 3.42994e-05 | 0.00414108 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803773 | TCCTCTTCTCAGAGG[A/G]GCTCTGGGGGGGCTC | 57602 |
rs753823427 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78815224 | GTAGTTCCAGCTACT[A/C]AGGAGGCTGAGGCAG | 57602 |
rs753827258 | snp | C/G | 1.6554e-05 | 0.00287693 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807305 | AGCTTAGGTGAGGTA[C/G]AGAGGACAACATCCC | 57602 |
rs753834011 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828348 | TTCTTTCTGCCAAGT[A/G]AATGTGAATGAGACT | 57602 |
rs753930867 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809856 | TTGCCCAGGCTGCTT[C/G]CTTTTTTTGAGATGG | 57602 |
rs753953143 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836170 | GCTCCCTCTGTTTTG[A/G]GGTTGAGCAACACAT | 57602 |
rs753955306 | snp | A/G | 0.000197765 | 0.00994201 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806212 | AGAGGTTTTCATGGG[A/G]TGGGTGAGGTCGGAG | 57602 |
rs753956242 | snp | A/G | 3.295e-05 | 0.00405881 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798491 | TCCGTCGAGTCTGAA[A/G]TTTCTGGAAGGCGTT | 57602 |
rs753979623 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812927 | TGATCTGGAATCACA[C/T]TCGGGCGGCCGGGAA | 57602 |
rs753996961 | snp | C/T | 1.66172e-05 | 0.00288242 | intron-variant | USP36 | GRCh38.p7 | 17:78818825 | ATGATTGATTCGTGC[C/T]CTGAAAAATGTTGTC | 57602 |
rs753998679 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799196 | ACGCCCATGTGTGGT[C/T]GGTCAGCATGGAACC | 57602 |
rs754008998 | snp | C/T | 3.50398e-05 | 0.00418553 | intron-variant | USP36 | GRCh38.p7 | 17:78803369 | TAGACAGATGCCACT[C/T]TGCTCCTGCCCTTAC | 57602 |
rs754015764 | snp | A/T | 1.65853e-05 | 0.00287964 | intron-variant | USP36 | GRCh38.p7 | 17:78798577 | AATCACAGGCATCAC[A/T]GTTCCCAAAAACGGC | 57602 |
rs754023740 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811010 | TTACAGCTACTCAGG[A/G]GGCAGAGGCAGGAGA | 57602 |
rs754050981 | in-del | -/GAA | 1.65056e-05 | 0.00287272 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828913 | TTTCAGGTCTCGGAT[-/GAA]GGAGACGGGCTTGAT | 57602 |
rs754092022 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796128 | ACCCCAGGAAAAGGT[C/T]TTACAGTTATCTAGT | 57602 |
rs754093133 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790791 | GCCATGTACTTAGAC[C/T]GTGTGTTGAAATCTG | 57602 |
rs754103720 | snp | C/T | 2.12841e-05 | 0.00326214 | intron-variant | USP36 | GRCh38.p7 | 17:78829049 | TTAAGACAAGAGCTT[C/T]CAAAGAACTCACGGT | 57602 |
rs754150793 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820631 | TGCAGCAGGATGTGC[A/G]ACAAAGCCAAGGCTG | 57602 |
rs754156750 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819986 | TTTCACAAAAAGTTC[C/T]AGAGCACGCACAATA | 57602 |
rs754175746 | snp | G/T | 3.50435e-05 | 0.00418575 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803890 | GTTCTGACGTCCCTG[G/T]GGGCTTGGGGGTACT | 57602 |
rs754178023 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825534 | TGGCCTCCCTCCTCT[C/T]TCCAGCAATCCTGGT | 57602 |
rs754238087 | snp | G/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812961 | AGGAGGAGCCTGTCC[G/T]GGAGATGAGGCCCTC | 57602 |
rs754262078 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791700 | AAGGCTGAAGAGGCA[A/G]GGGGGATCTGGATCA | 57602 |
rs754264254 | snp | A/G | 0.000135642 | 0.00823422 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827283 | TTTCTGCATGGCGTC[A/G]ATGGTGTACCGCAGG | 57602 |
rs754265841 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833856 | CTTATTATTGTTATC[C/T]GAGTTATAGGAACTT | 57602 |
rs754284939 | snp | C/T | 4.94352e-05 | 0.00497143 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836247 | TGGCTCGAACTCGAT[C/T]TTCTGTAAAAGGACC | 57602 |
rs754288528 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78816636 | GTCTCAAAAAAAAAA[A/C]CAAAAAAACCAAAAT | 57602 |
rs754338468 | snp | G/T | 6.49963e-05 | 0.00570034 | intron-variant | USP36 | GRCh38.p7 | 17:78827223 | TCCAAAGCCCTGGGA[G/T]GGTGGGTGGGGAAGC | 57602 |
rs754346385 | snp | C/G | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807393 | TCCCAGGCAGCCCCT[C/G]AGCAGTTCTGGGGGA | 57602 |
rs754369153 | snp | A/G | 4.96644e-05 | 0.00498294 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807166 | CCTGGGGGTCTGGGG[A/G]GCCTTGGTGGAGTCG | 57602 |
rs754474833 | snp | G/T | 3.30874e-05 | 0.00406726 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807479 | GTTGGCATGTGTGTG[G/T]GTGTCTGGGAGAGTT | 57602 |
rs754486039 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823101 | TCTCATCTGGCCTGT[C/G]TGACTATTTACCATG | 57602 |
rs754486964 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788109 | GCAGCCTCAGGAAGC[A/G]AGTACATGAAGCTCT | 57602 |
rs754530045 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78805227 | TATAAGGGCCATGCC[-/A]AGCTGCACGATGTTT | 57602 |
rs754553649 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815277 | GTGGAGGTTACAGTG[A/G]GCCGAGATCATACCA | 57602 |
rs754569051 | snp | A/C | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807426 | AGTGCTGTGGAGGAG[A/C]TGGCTTCTTCACCTT | 57602 |
rs754573806 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822522 | CTCCCCGGCTCTGCA[C/T]CCGTCTCAGAGAGGA | 57602 |
rs754581673 | snp | A/G | 1.65337e-05 | 0.00287517 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799737 | AGACTCCCGCTCTCC[A/G]TTCCAAGACACAGGA | 57602 |
rs754582460 | snp | A/G | 3.29826e-05 | 0.00406082 | intron-variant | USP36 | GRCh38.p7 | 17:78820034 | AGGACAAAAACAGGG[A/G]GTAAAATACACAGCA | 57602 |
rs754659416 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814522 | GGGACATATACGGAC[A/G]TATGTTGAGGAATTC | 57602 |
rs754671396 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828351 | TTTCTGCCAAGTGAA[A/T]GTGAATGAGACTTTT | 57602 |
rs754681589 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | USP36 | GRCh38.p7 | 17:78813004 | AGAGCCTGGAATTCT[A/G]TCAAAGGAAGAAAAC | 57602 |
rs754689017 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798318 | ACATCATACACACAC[A/G]CCACACCCCACCACA | 57602 |
rs754701483 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796674 | AGGGGGTGCAGACAG[C/T]GAGGCAGCCACCCGG | 57602 |
rs754709818 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78838735 | AACACCGAAGCCGCA[C/G]AGCGGGCGTCAGAGC | 57602 |
rs754746703 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793884 | GCCTACTTCCCATGC[C/T]TAGGATTCTCCCTGG | 57602 |
rs754795412 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837550 | CAGAGGATCGATACT[A/G]TTGGTGCAGCTGCAT | 57602 |
rs754797798 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798928 | CTCGGTCAAACTCTT[C/T]GTCCCAGTCATCAAC | 57602 |
rs754840091 | snp | C/G | 1.66092e-05 | 0.00288172 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836375 | GCATGGTGCATCACT[C/G]TGGGGACAAGAAGAA | 57602 |
rs754847185 | snp | A/G | 5.00751e-05 | 0.0050035 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78820993 | GACAGATCTGTACCC[A/G]GATCTCCAGCGCGAC | 57602 |
rs754865601 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818896 | GTGGAATCTTCATCA[A/G]TGAGATTTCGACCTT | 57602 |
rs754935178 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829209 | TCTCTGCTGGATGGC[A/G]TTTGGAAGCTATGAT | 57602 |
rs754941591 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793047 | AAGGCTTTAAATGCT[C/G]ATGCCTAAGCCTCAC | 57602 |
rs754944329 | snp | C/T | 2.34036e-05 | 0.00342071 | intron-variant | USP36 | GRCh38.p7 | 17:78827380 | AGGGAGGGAAGAGCT[C/T]GTGTCTTCTCATCAA | 57602 |
rs754956173 | snp | C/T | 1.65288e-05 | 0.00287474 | intron-variant | USP36 | GRCh38.p7 | 17:78798860 | GGCTCTGAGCTGAGC[C/T]ACGCCGCCCTGCTCC | 57602 |
rs754958212 | snp | C/T | 1.66363e-05 | 0.00288407 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803623 | CCTCCTGCAGGGCGC[C/T]GGCAGCTGTGTCCTC | 57602 |
rs754993058 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | USP36 | GRCh38.p7 | 17:78818651 | AGCTGCCTGGGATGG[C/T]GTCACGAGCGCTCAC | 57602 |
rs755036393 | snp | A/G | 0.0001009 | 0.00710209 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802373 | TGGTGCGCAGCTGCT[A/G]GACTCGGGGACAACA | 57602 |
rs755037030 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787749 | TCCCAACAAAAGATA[C/T]GTTGAAGTCCTAAGC | 57602 |
rs755107337 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818731 | GTTAAGACGTTGGAT[A/G]TTCTGTGGATGGTGA | 57602 |
rs755178802 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833887 | TATAGAATGAGCTGG[A/G]AAAGATTCTCTCCTC | 57602 |
rs755241349 | snp | C/T | 1.76142e-05 | 0.00296762 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803902 | CTGGGGGCTTGGGGG[C/T]ACTGGACAGCAATGT | 57602 |
rs755243023 | snp | A/G | 1.66732e-05 | 0.00288727 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807231 | AGCCCCTCCTGTCGA[A/G]GCCAGCGCTCTCGTC | 57602 |
rs755285118 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826130 | GCAAGGAAGCTTGAG[C/T]CCCTTCAGGAGAAGG | 57602 |
rs755292071 | snp | G/T | 1.94998e-05 | 0.00312242 | intron-variant | USP36 | GRCh38.p7 | 17:78803984 | TGACACAGCCCTGTG[G/T]GGACAGCCAGGAAAC | 57602 |
rs755294264 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809940 | CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 57602 |
rs755295847 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816741 | CTCAGCCTCCCTAAG[C/T]GCTGACATTAGAGTT | 57602 |
rs755297384 | snp | G/T | 1.65833e-05 | 0.00287948 | intron-variant | USP36 | GRCh38.p7 | 17:78812834 | CCAAGACCAGCCACT[G/T]TGGCCTCCATCATTC | 57602 |
rs755311350 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800302 | AGGGGTGGAGGGAAC[A/G]GCCAAGCTTGGCTGC | 57602 |
rs755339117 | snp | A/C/T | 8.2627e-05 | 0.00642712 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836067 | CCATCCACTTCGTCA[A/C/T]CCCGGAGTGAGGGCC | 57602 |
rs755347866 | in-del | -/TCTTCC | 6.76888e-05 | 0.0058172 | cds-indel, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803652 | CCGGGCGCTTCTTCT[-/TCTTCC]TCTTCCTCTTCCTCT | 57602 |
rs755365426 | in-del | -/TTC | 4.94254e-05 | 0.00497094 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812900 | ATCCCATTGCCGATG[-/TTC]TTCTTGGAGTGATCT | 57602 |
rs755373712 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789750 | CTGGCCACGTGCCAC[A/G]GTTTGGGCGTTCACT | 57602 |
rs755375185 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825556 | AATCCTGGTACCAAC[A/G]AATGGCTCACCACCA | 57602 |
rs755386241 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78838147 | CAGCACTTGGGAGGC[C/T]GAGACGGGTGGATCA | 57602 |
rs755386999 | snp | A/G | 1.70571e-05 | 0.00292032 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803721 | GGGAGGCGCGTCTCT[A/G]AGCCCAGCCTCTGCG | 57602 |
rs755446169 | snp | C/T | 1.91749e-05 | 0.0030963 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802460 | CCGCTGTGTCTCCTG[C/T]TTTCTTTTTTTCTTT | 57602 |
rs755469294 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822574 | TCGGGGTCAGGAGCC[C/T]TGCCCTCATTCATGT | 57602 |
rs755550563 | snp | A/G | 4.75161e-05 | 0.00487399 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821004 | ACCCGGATCTCCAGC[A/G]CGACGTCCAAGTAGG | 57602 |
rs755573541 | snp | A/G/T | 1.6486e-05 | 0.00287102 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835486 | TCACCACAGCTCTCA[A/G/T]ACGTGTGCTCACTGC | 57602 |
rs755576691 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78793438 | GAATCCATGGCACCC[-/A]AGATGATCTTCTCCA | 57602 |
rs755645646 | snp | C/T | 3.33879e-05 | 0.00408568 | intron-variant | USP36 | GRCh38.p7 | 17:78806947 | GCAGCGGCGAGACCC[C/T]CACACACCCACCTTC | 57602 |
rs755800484 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78835822 | CATGCAGCCCACCCC[A/G]TTTCTCTTTCTTAGT | 57602 |
rs755801479 | snp | A/G/T | 3.44117e-05 | 0.00414788 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807562 | CTTCAGGCCCAGGGT[A/G/T]GAGCCATTCCTGGAT | 57602 |
rs755805162 | snp | C/G | 4.95454e-05 | 0.00497697 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806277 | CGGTCGCCCTCCACA[C/G]GGTGCTGGCCTGCAG | 57602 |
rs755813219 | snp | C/T | 3.335e-05 | 0.00408337 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807239 | CTGTCGAGGCCAGCG[C/T]TCTCGTCGTTCCCCT | 57602 |
rs755823848 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816054 | CTGGCATGGCAGCTG[C/T]AGGCTGAGTGCACCA | 57602 |
rs755890408 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78804294 | TGGTGAAACCCCATC[C/T]CTACTAAAAATACAA | 57602 |
rs755909702 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78823048 | TTCCACACCCGCAGG[A/C]TACACTTCCCCTCCC | 57602 |
rs755939658 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807289 | AGTGGCTGTAGCCAG[A/G]AGCTTAGGTGAGGTA | 57602 |
rs755975657 | snp | A/G | 2.02092e-05 | 0.00317871 | intron-variant | USP36 | GRCh38.p7 | 17:78804001 | GACAGCCAGGAAACA[A/G]GGAGAGGATGTTCTG | 57602 |
rs755997443 | in-del | -/CAAA | | | intron-variant | USP36 | GRCh38.p7 | 17:78828213 | AGCAAAACCCTGTCT[-/CAAA]CAAAAAGAATGTAAA | 57602 |
rs756000828 | snp | A/G | 2.65488e-05 | 0.00364331 | intron-variant | USP36 | GRCh38.p7 | 17:78827398 | GTCTTCTCATCAAAC[A/G]GCCTGCGGCTGCTTT | 57602 |
rs756027164 | snp | A/T | 1.64982e-05 | 0.00287208 | intron-variant | USP36 | GRCh38.p7 | 17:78813750 | GGGAGTGAGCTCATC[A/T]GGGGAGGGCGTGAGT | 57602 |
rs756056988 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798998 | ATCCTGACTGACCGC[C/T]GACATCTTGCCATCC | 57602 |
rs756068357 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837323 | GTCTTCCCAGGACTC[C/T]TATCAAAAGAGAAGA | 57602 |
rs756076550 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798936 | AACTCTTCGTCCCAG[C/T]CATCAACCACGGTCT | 57602 |
rs756087351 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814283 | CAGAGAGGCAACAAC[A/G]AGGACTTGAATACAA | 57602 |
rs756141340 | snp | A/C | 2.01011e-05 | 0.0031702 | intron-variant | USP36 | GRCh38.p7 | 17:78807670 | AAAACACAACTGAGG[A/C]AGCGAGAAGTCTCAG | 57602 |
rs756148164 | snp | A/G | 1.66443e-05 | 0.00288477 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836386 | CACTGTGGGGACAAG[A/G]AGAAACATAGAGCCA | 57602 |
rs756167314 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822961 | TCCCCAGCTGCTTCC[C/G]CGACTCCTCACTGGC | 57602 |
rs756194766 | snp | A/T | 4.96364e-05 | 0.00498154 | intron-variant | USP36 | GRCh38.p7 | 17:78812844 | CCACTTTGGCCTCCA[A/T]CATTCTCACAAATAC | 57602 |
rs756208436 | in-del | -/CTTGGGGGCGCAAGCAGACTACGTTTCCAGACCATACCTA | 1.67947e-05 | 0.00289777 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803893 | TGACGTCCCTGGGGG[lengthTooLong]CTTGGGGGTACTGGA | 57602 |
rs756286998 | snp | C/T | 1.64787e-05 | 0.00287038 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798405 | CGGAACCGACCTCCT[C/T]CCACAGGGGCACAGT | 57602 |
rs756295889 | in-del | -/CA | 1.65244e-05 | 0.00287436 | intron-variant | USP36 | GRCh38.p7 | 17:78813730 | GGTATAAGAAAAGAG[-/CA]CAGAGGGAGTGAGCT | 57602 |
rs756297851 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792856 | CCCAAGTAGTTGGGA[G/T]TACAGGCACAGGCCA | 57602 |
rs756303631 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828250 | CATTGAATATCTCTC[C/G]AAAAGCCAATATAAA | 57602 |
rs756312839 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793788 | TAACAGTATGTTAGG[A/G]ATAAACAGATGCCCA | 57602 |
rs756334749 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818748 | TCTGTGGATGGTGAA[A/G]CGCTTGCTGGCTGGA | 57602 |
rs756341047 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791951 | GACAGAGGGTGGATC[A/G]GTCGGCTGTTCAGTG | 57602 |
rs756344934 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806157 | GGCCCAAAGCTTACC[C/T]GGCTCTATGGACGGG | 57602 |
rs756363171 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839847 | ACCCAACTCAGGAAG[A/G]ATGCTCTCTCTTGTC | 57602 |
rs756409611 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819870 | GCACAACACTGTCAG[A/G]TGAGGGGACTTATTT | 57602 |
rs756444529 | snp | C/T | 1.80146e-05 | 0.00300116 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802486 | TCTTTTTCTTTTTCC[C/T]TGGAGACTCTTCCAT | 57602 |
rs756445173 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824334 | AGTAAAGGGTACCAC[A/G]GTGGACTGCCAAATC | 57602 |
rs756447523 | snp | C/T | 1.72421e-05 | 0.00293611 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803830 | GAGACACAAGGTCCT[C/T]GTTGACCTGAGGCAG | 57602 |
rs756586211 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809825 | ATGGGGTTTTGGAGA[C/T]GGGGGTCTTTCTATG | 57602 |
rs756602134 | snp | G/T | 0.000115529 | 0.00759942 | intron-variant | USP36 | GRCh38.p7 | 17:78827221 | TGTCCAAAGCCCTGG[G/T]AGGGTGGGTGGGGAA | 57602 |
rs756616273 | snp | A/G | 1.65151e-05 | 0.00287355 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814423 | TCACCTTCACGTAGC[A/G]GTAATAGTGCCCGGC | 57602 |
rs756624536 | snp | A/C/G | 3.29501e-05 | 0.00405884 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798486 | GAAGTTCCGTCGAGT[A/C/G]TGAAGTTTCTGGAAG | 57602 |
rs756645192 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810152 | TAGACAAGGTCTCAC[-/T]CTGTCACCTTGCCTG | 57602 |
rs756676662 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799174 | AGGACAAGAGGAGGA[C/T]GGCTCGACGCCCATG | 57602 |
rs756686721 | snp | A/C/G | 3.42996e-05 | 0.00414112 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803781 | TCAGAGGGGCTCTGG[A/C/G]GGGGCTCACTGGCCT | 57602 |
rs756719722 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78840051 | TCCCGGGGCCCAGCG[A/C]CGCGCTCCAGGGGCC | 57602 |
rs756810801 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815882 | GTACGCATATACATA[C/T]ATGCACAACACATAC | 57602 |
rs756818211 | snp | C/G | 3.29516e-05 | 0.00405891 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799017 | ATCTTGCCATCCCAG[C/G]TCAGAACTACCAGGC | 57602 |
rs756825733 | snp | C/T | 1.65364e-05 | 0.0028754 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813860 | TTCATCTGGTACCAC[C/T]GTCCATTGCTTGCCT | 57602 |
rs756853239 | snp | C/T | 0.000188869 | 0.0097159 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803777 | CTTCTCAGAGGGGCT[C/T]TGGGGGGGCTCACTG | 57602 |
rs756955437 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807043 | GTTGCTCAGGACAGG[A/G]GACTTCAGCTTCACC | 57602 |
rs756999350 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78821844 | GGTCTGCACAGCGAA[A/G]AAAGAGCCCCAGCCT | 57602 |
rs757006681 | snp | C/T | 3.4114e-05 | 0.00412987 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803714 | GTGCTGTGGGAGGCG[C/T]GTCTCTGAGCCCAGC | 57602 |
rs757013432 | snp | C/G | 1.83707e-05 | 0.00303068 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802510 | CTTCCATGGCCTCTG[C/G]ATCACCATCACCCAT | 57602 |
rs757063261 | snp | A/G | 1.6522e-05 | 0.00287414 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828961 | GGCGAAGGCCTGGAC[A/G]ATGTGGTTCTGCATG | 57602 |
rs757078974 | snp | A/C | 1.65356e-05 | 0.00287533 | intron-variant | USP36 | GRCh38.p7 | 17:78799634 | AAACCAACCAATGAA[A/C]GGCAAACAGAAGTCC | 57602 |
rs757086258 | snp | G/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806213 | GAGGTTTTCATGGGG[G/T]GGGTGAGGTCGGAGG | 57602 |
rs757127360 | in-del | -/CTGC | | | intron-variant | USP36 | GRCh38.p7 | 17:78792687 | CAACTCTCAACTCTG[-/CTGC]TCACTATGATCCCCC | 57602 |
rs757163190 | snp | A/G | 3.30961e-05 | 0.0040678 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807309 | TAGGTGAGGTAGAGA[A/G]GACAACATCCCTGCT | 57602 |
rs757196426 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796549 | GAGACACCCACCCAC[A/G]TGGAAAAAAATAAAT | 57602 |
rs757241345 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834639 | GTAGAAACCGGGTTT[C/T]GCCATGTTGGCCAGG | 57602 |
rs757285017 | snp | C/T | 6.60884e-05 | 0.00574803 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807144 | CGCAGAGATGGGCCG[C/T]TCCACTCCTGGGGGT | 57602 |
rs757312094 | in-del | -/G | 0.000148363 | 0.00861159 | intron-variant | USP36 | GRCh38.p7 | 17:78818649 | GGAGCTGCCTGGGAT[-/G]GTGTCACGAGCGCTC | 57602 |
rs757370811 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836249 | GCTCGAACTCGATTT[G/T]CTGTAAAAGGACCTT | 57602 |
rs757381378 | in-del | -/T | 2.04405e-05 | 0.00319685 | intron-variant | USP36 | GRCh38.p7 | 17:78829047 | TTTTAAGACAAGAGC[-/T]TTCAAAGAACTCACG | 57602 |
rs757393172 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826442 | ACAGAGCAAGACTCC[C/T]GTCTCAAAAGCAGTT | 57602 |
rs757440797 | snp | C/G | 8.29304e-05 | 0.00643882 | intron-variant | USP36 | GRCh38.p7 | 17:78798578 | ATCACAGGCATCACA[C/G]TTCCCAAAAACGGCT | 57602 |
rs757447327 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78835648 | TGTTCTGGTTTACAG[C/G]ACATTCCTGGAAAGC | 57602 |
rs757466384 | snp | A/G | 0.000214608 | 0.0103565 | intron-variant | USP36 | GRCh38.p7 | 17:78812855 | TCCATCATTCTCACA[A/G]ATACCTTTCCAGTCA | 57602 |
rs757493080 | snp | C/T | 5.24288e-05 | 0.00511973 | intron-variant | USP36 | GRCh38.p7 | 17:78803372 | ACAGATGCCACTTTG[C/T]TCCTGCCCTTACCTG | 57602 |
rs757499167 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824507 | GGAGATTGCACCACT[A/G]CACTCTAGCCTGGGA | 57602 |
rs757528298 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792011 | GGCTTGATCTAGAGT[A/T]TGCAGCAAATGCAAC | 57602 |
rs757533435 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819993 | AAAAGTTCCAGAGCA[C/T]GCACAATATTCGCAG | 57602 |
rs757604489 | snp | A/G | 1.65542e-05 | 0.00287695 | intron-variant | USP36 | GRCh38.p7 | 17:78798560 | TCTTTTCCTAGACCA[A/G]GAATCACAGGCATCA | 57602 |
rs757626090 | snp | A/G/T | 4.95203e-05 | 0.00497575 | intron-variant | USP36 | GRCh38.p7 | 17:78818637 | ACTGTGGCCCACGGA[A/G/T]CTGCCTGGGATGGTG | 57602 |
rs757708819 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808159 | TTCTTTTTTCAATCT[G/T]TTCTTCCAAATGGTT | 57602 |
rs757747598 | snp | C/T | 3.45328e-05 | 0.00415514 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803837 | AAGGTCCTCGTTGAC[C/T]TGAGGCAGCGCCGTC | 57602 |
rs757795848 | snp | C/T | 1.65288e-05 | 0.00287474 | stop-gained, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807329 | ACATCCCTGCTGTCC[C/T]AGGAGCCCTGCCTTT | 57602 |
rs757796841 | snp | A/G | 3.50392e-05 | 0.00418549 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803892 | TCTGACGTCCCTGGG[A/G]GCTTGGGGGTACTGG | 57602 |
rs757798826 | snp | A/C | 0.000116228 | 0.00762236 | intron-variant | USP36 | GRCh38.p7 | 17:78799773 | CTGGCTCAGCCCTGC[A/C]ATCGGAGCAGCCAAG | 57602 |
rs757799708 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829675 | TTATTTACACACACA[C/G]AGAGCAGGCCAGATG | 57602 |
rs757820844 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808896 | CCTGTACTTAGTACT[C/G]CATGCTAATTTTCTG | 57602 |
rs757877788 | snp | G/T | 1.6552e-05 | 0.00287676 | intron-variant | USP36 | GRCh38.p7 | 17:78814408 | ACTGACACAAGCCTC[G/T]CACCTTCACGTAGCA | 57602 |
rs757916919 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805894 | TCACCACAAGGATGT[C/T]GCAGACAGACCACCA | 57602 |
rs757933013 | snp | A/G | 4.9507e-05 | 0.00497504 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807412 | AGTTCTGGGGGAAAA[A/G]TGCTGTGGAGGAGCT | 57602 |
rs757956896 | snp | A/G | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813868 | GTACCACTGTCCATT[A/G]CTTGCCTGAAGCAGC | 57602 |
rs757967737 | snp | C/G | 3.47494e-05 | 0.00416815 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78829006 | GAAGCTTCCCTGGTG[C/G]CCTGCCGGCGTGGAA | 57602 |
rs757969710 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830613 | CCTATTATCTATTAT[C/T]AAATAGATCCATCTC | 57602 |
rs758014075 | snp | C/T | 3.30573e-05 | 0.00406541 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799729 | ACCACATCAGACTCC[C/T]GCTCTCCATTCCAAG | 57602 |
rs758075673 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820379 | CTGTGTGGGAGGATC[A/G]CTTAAGCCTAGAGGT | 57602 |
rs758085506 | in-del | -/TTTTTTTTTTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78791131 | CCAATCTGGCCTTCT[-/TTTTTTTTTTTT]TTTTTTTTTTAGCTG | 57602 |
rs758201748 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78820005 | GCACGCACAATATTC[A/G]CAGCTTGCTGAGGAG | 57602 |
rs758215486 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803510 | CTGCTGGCCATTCAC[C/T]TGTGGCTGTGTGCCA | 57602 |
rs758255576 | snp | A/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807468 | CGTCTAGGATGGTTG[A/G]CATGTGTGTGGGTGT | 57602 |
rs758272310 | snp | G/T | 5.77034e-05 | 0.00537107 | intron-variant | USP36 | GRCh38.p7 | 17:78820974 | CTGCAAAAGTGAAGG[G/T]CAGGACAGATCTGTA | 57602 |
rs758294575 | snp | C/G | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795395 | GAGCCACACACATCA[C/G]GTAACAGCTGCAGAG | 57602 |
rs758313435 | in-del | -/G | 7.74084e-05 | 0.00622079 | intron-variant | USP36 | GRCh38.p7 | 17:78835540 | AGAAAAGAGGAAGAC[-/G]TAAGTCCACACACAG | 57602 |
rs758356046 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820779 | CACAAAACCCAATTT[A/T]ACCATTTTTTTCTTT | 57602 |
rs758371951 | snp | C/G | 1.65707e-05 | 0.00287838 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807172 | GGTCTGGGGGGCCTT[C/G]GTGGAGTCGCTGCTG | 57602 |
rs758375273 | snp | A/G | 1.64996e-05 | 0.0028722 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806260 | TGGACGGAGGTCATT[A/G]CCGGTCGCCCTCCAC | 57602 |
rs758375326 | snp | C/G | 1.67167e-05 | 0.00289103 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803405 | CCGAAGTGGGTCCTG[C/G]TGCAGGCCGCCTTCT | 57602 |
rs758416389 | snp | A/C/G | 3.31572e-05 | 0.00407157 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836365 | TCCACTATTGGCATG[A/C/G]TGCATCACTGTGGGG | 57602 |
rs758418594 | snp | C/G/T | 0.00388787 | 0.0439183 | intron-variant | USP36 | GRCh38.p7 | 17:78827230 | CCCTGGGAGGGTGGG[C/G/T]GGGGAAGCACGCACT | 57602 |
rs758423834 | snp | C/T | 0.000210874 | 0.0102661 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803896 | ACGTCCCTGGGGGCT[C/T]GGGGGTACTGGACAG | 57602 |
rs758532602 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833921 | TATTCTTTGGAAGAA[C/T]GTGTAAAGGATTGGA | 57602 |
rs758535415 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78803011 | TGACGCGATCTCAGC[G/T]CACTGCAACCTCCAC | 57602 |
rs758541447 | snp | C/T | 1.69332e-05 | 0.0029097 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827293 | GCGTCGATGGTGTAC[C/T]GCAGGAACTCATGCG | 57602 |
rs758577833 | snp | A/G | 1.66065e-05 | 0.00288149 | intron-variant | USP36 | GRCh38.p7 | 17:78798590 | ACAGTTCCCAAAAAC[A/G]GCTCTTTCCTGGCCC | 57602 |
rs758604956 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798920 | TACCTTCCCTCGGTC[A/G]AACTCTTCGTCCCAG | 57602 |
rs758623047 | snp | C/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807151 | ATGGGCCGCTCCACT[C/G]CTGGGGGTCTGGGGG | 57602 |
rs758640017 | in-del | -/AGA | | | intron-variant | USP36 | GRCh38.p7 | 17:78806454 | GGGCAGGGGAATGGT[-/AGA]AGAAGAACCAGAAAA | 57602 |
rs758654740 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836271 | AAGGACCTTCTTGGC[A/G]GAGGAGGCAAGAAGC | 57602 |
rs758671736 | snp | A/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812984 | AGGCCCTCGGGACTT[A/T]TCTTAGAGCCTGGAA | 57602 |
rs758693190 | snp | C/T | 1.85848e-05 | 0.00304828 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807621 | GCGGCTTCTTCATCG[C/T]CCCAGAGTCTTGTCG | 57602 |
rs758718960 | snp | G/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841915 | AAATTCACCTTGTAT[G/T]TATTACCTGGGCGCT | 57602 |
rs758730913 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801503 | GCTCGGCCCCCTATA[C/T]CAAGCAGCCAGGACT | 57602 |
rs758733575 | snp | C/T | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819997 | GTTCCAGAGCACGCA[C/T]AATATTCGCAGCTTG | 57602 |
rs758733744 | snp | A/T | 9.51973e-05 | 0.00689852 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835467 | CTGCGGGGCTGGGAC[A/T]CCGTCACCACAGCTC | 57602 |
rs758741298 | snp | A/T | 1.72397e-05 | 0.00293591 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807564 | TCAGGCCCAGGGTGG[A/T]GCCATTCCTGGATAT | 57602 |
rs758907001 | in-del | -/ACACAT | 1.64882e-05 | 0.00287121 | cds-indel, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803484 | TGGTGGCCGTCCGTA[-/ACACAT]CCCACCTGCTGGCCA | 57602 |
rs758931724 | snp | C/T | 1.93358e-05 | 0.00310927 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827346 | GAAGTGTCGGGCGAT[C/T]TCTAAAAGAGGAAGA | 57602 |
rs758948933 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817774 | AAGAAAAAAGAAACA[C/T]ATCTTCTATGAAAAT | 57602 |
rs758997026 | snp | G/T | 1.64993e-05 | 0.00287218 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802351 | CAGGACACCAGCCAT[G/T]CGCGGATGGTGCGCA | 57602 |
rs759005443 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833358 | GTGATCTCAGCTCAA[C/T]GCAACCTCTGCCTCC | 57602 |
rs759033918 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788927 | AGATGAGGCCAGGTG[C/T]GGTGACTCACGCCTG | 57602 |
rs759064890 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832990 | TTCGTCTCTACTAAA[A/G]ATACAAAATTAGCCA | 57602 |
rs759081301 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | USP36 | GRCh38.p7 | 17:78818628 | CTGATGCCGACTGTG[A/G]CCCACGGAGCTGCCT | 57602 |
rs759134548 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818688 | GATCTTCCCCCCGCT[C/G]AAGTTGGCAAAGCGC | 57602 |
rs759180087 | snp | A/G | 3.33172e-05 | 0.00408136 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807207 | AGTGCTCTGGGCTGG[A/G]GCTGCTGGAGCCCCT | 57602 |
rs759184067 | snp | C/T | 1.74717e-05 | 0.00295559 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803885 | CCGTGGTTCTGACGT[C/T]CCTGGGGGCTTGGGG | 57602 |
rs759214768 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809620 | GTTCCTGTGGCAAGT[A/G]GGGCTTCCTTTGTTT | 57602 |
rs759220984 | in-del | -/TGCTGGACTCGGGGACAACAGCATCT | 3.62785e-05 | 0.00425887 | frameshift-variant, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802369 | CGGATGGTGCGCAGC[-/TGCTGGACTCGGGGACAACAGCATCT]TGGGGCTTGGCACTC | 57602 |
rs759229493 | snp | C/T | 8.50637e-05 | 0.00652109 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827279 | AGGCTTTCTGCATGG[C/T]GTCGATGGTGTACCG | 57602 |
rs759234859 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816080 | CACCAGGACAGCACA[A/G]AGCCCACATGACAGG | 57602 |
rs759262288 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823884 | CTGGATACGAATCTT[C/G]AAAACCAGCCGACCC | 57602 |
rs759282423 | snp | A/G | 5.93983e-05 | 0.00544937 | intron-variant | USP36 | GRCh38.p7 | 17:78835525 | GAAAGGGACAAGGGA[A/G]GAAAAGAGGAAGACG | 57602 |
rs759332450 | snp | C/T | 5.1113e-05 | 0.00505508 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821038 | CGTAGGTGTCCGAGA[C/T]GCTCTTGCACACGGA | 57602 |
rs759347781 | snp | C/T | 1.72104e-05 | 0.00293341 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803681 | CTTCCCGTGGGGAGC[C/T]GCAGTGGCCTCCCTG | 57602 |
rs759457038 | snp | C/T | 1.94483e-05 | 0.00311829 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802427 | TGGGCATTTGAGATG[C/T]CCATCCTCTTCTACT | 57602 |
rs759464261 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839569 | AGAACCACTTAGGGA[A/G]GGGATAAACGAACCT | 57602 |
rs759531943 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835077 | TACAGAAAAGCTTGG[C/T]GAACACAGCCCCACC | 57602 |
rs759552605 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836825 | CACACACACAAACGG[-/AC]ACACACACACACACC | 57602 |
rs759557030 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807015 | ACATGGTGCTTGCAG[A/G]CTCAGTGGTGGTGTT | 57602 |
rs759576646 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796965 | GTAATCTTCTTGAGT[C/T]ATACAATCATTTAAA | 57602 |
rs759593926 | in-del | -/AC | | | intron-variant | USP36 | GRCh38.p7 | 17:78831594 | ACTCCAGCATAAGCA[-/AC]AGAGACTCTGTCTCA | 57602 |
rs759610534 | snp | A/G | 0.000136806 | 0.00826948 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803748 | TGCGGCTCTCCCACA[A/G]AGGTCTTTTTCCTCT | 57602 |
rs759663788 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78830300 | ACGTATCATTCAGCA[A/C]TGGCTTTACAAAAAT | 57602 |
rs759684255 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78831942 | GTGAGAGCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 57602 |
rs759688944 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798979 | GTCTGCTGTCTTCAA[C/T]AGCATCCTGACTGAC | 57602 |
rs759714003 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807378 | TATTCGAGTTGCTGG[C/T]CCCAGGCAGCCCCTG | 57602 |
rs759749577 | in-del | -/CA | | | intron-variant | USP36 | GRCh38.p7 | 17:78798205 | TATACACACGCATCC[-/CA]CACACACCCTTCTCC | 57602 |
rs759774954 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796247 | TACAGAACATCACAC[A/G]GTAAACATGGCAGAG | 57602 |
rs759795822 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | USP36 | GRCh38.p7 | 17:78822048 | AAGGGCTCAGCAAGA[C/T]GACACGAGGGATGGC | 57602 |
rs759811318 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | USP36 | GRCh38.p7 | 17:78799063 | CACGAGTGCAGGTTC[C/T]CAGGTCCCCTGTGGC | 57602 |
rs759842188 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819957 | TAGGCATTCTCTCCA[C/T]TCAGGACATCTGCTT | 57602 |
rs759880106 | snp | C/T | 3.32651e-05 | 0.00407817 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807276 | CATGCCCGTTGGCAG[C/T]GGCTGTAGCCAGGAG | 57602 |
rs759909816 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812906 | TTGCCGATGTTCTTC[C/T]TGGAGTGATCTGGAA | 57602 |
rs759951256 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842335 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 57602 |
rs760003598 | snp | A/G | 4.95618e-05 | 0.00497779 | intron-variant | USP36 | GRCh38.p7 | 17:78818798 | GAAGAAGGTGATGAG[A/G]AAGATTAATGAATGA | 57602 |
rs760010435 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792557 | TGCACATTCTCAGGC[C/T]TCATCCCAGACCTGC | 57602 |
rs760032688 | in-del | -/GGGGG/GGGGGG | 9.07615e-05 | 0.00673601 | intron-variant | USP36 | GRCh38.p7 | 17:78827230 | CCTGGGAGGGTGGGT[-/GGGGG/GGGGGG]GGGGAAGCACGCACT | 57602 |
rs760056351 | snp | A/G | 1.64822e-05 | 0.00287068 | intron-variant | USP36 | GRCh38.p7 | 17:78818781 | CTTCTTCTTGCATCT[A/G]TGAAGAAGGTGATGA | 57602 |
rs760057760 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812418 | ACATTGGCCGGGCGC[A/G]GTGGCTCATGCCTGT | 57602 |
rs760068780 | snp | C/T | 1.64901e-05 | 0.00287137 | intron-variant | USP36 | GRCh38.p7 | 17:78798380 | CACCTCACCCTTACA[C/T]CCACCCCCTCGGAAC | 57602 |
rs760114925 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806196 | AGGCAACGACGGGGT[A/G]AGAGGTTTTCATGGG | 57602 |
rs760142852 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818518 | GCGAAACTACAGTCC[C/G]TACTTCACAATATGT | 57602 |
rs760145627 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802762 | TCCTAACTGAGCCAA[A/G]CCTGTTGACGCCAAT | 57602 |
rs760166513 | in-del | -/A | 3.57121e-05 | 0.00422549 | intron-variant | USP36 | GRCh38.p7 | 17:78803348 | GCTTTGTTTCTCGTC[-/A]AGAGGTAGACAGATG | 57602 |
rs760172673 | snp | C/G | 3.4984e-05 | 0.0041822 | intron-variant | USP36 | GRCh38.p7 | 17:78835544 | AAGAGGAAGACGTAA[C/G]TCCACACACAGGTCG | 57602 |
rs760257019 | snp | C/T | 3.29533e-05 | 0.00405901 | intron-variant | USP36 | GRCh38.p7 | 17:78806123 | CACAGGGAGAACCAG[C/T]TGGCACCCAGAAGAT | 57602 |
rs760265433 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817371 | TAAGCAAGCCCCCAC[C/T]ACTACCAGTGAGGAA | 57602 |
rs760270597 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807034 | AGTGGTGGTGTTGCT[C/G]AGGACAGGGGACTTC | 57602 |
rs760272715 | snp | C/G | 1.66671e-05 | 0.00288674 | intron-variant | USP36 | GRCh38.p7 | 17:78812814 | GAGGAGGTCTGTGAG[C/G]AGCACCAAGACCAGC | 57602 |
rs760294797 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819439 | TGACAAAGTAAGAGT[C/T]CTATCTGCAGAAACG | 57602 |
rs760314946 | in-del | -/CGAGTGCTCTGGGCTGGAGCTGCTGGA | 1.66272e-05 | 0.00288328 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807190 | GGAGTCGCTGCTGGC[-/CGAGTGCTCTGGGCTGGAGCTGCTGGA]GCCCCTCCTGTCGAG | 57602 |
rs760379706 | snp | A/G | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78786923 | AAAGGTTTTAAGCAG[A/G]GGTAACCCAAAATAT | 57602 |
rs760391902 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78800135 | AAAAAGCTAAAAACC[-/A]AAAAAAAAAAAACCC | 57602 |
rs760410913 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808025 | CATATCTTTATGGCC[A/G]CCTTTACTATAAAAC | 57602 |
rs760415964 | snp | C/T | 1.7161e-05 | 0.0029292 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803788 | GGCTCTGGGGGGGCT[C/T]ACTGGCCTCTGGCAA | 57602 |
rs760453200 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78815134 | GTCAAGAGATTGAGA[A/C]CATCGTGGCCAAGAT | 57602 |
rs760465397 | snp | C/T | 4.98815e-05 | 0.00499382 | intron-variant | USP36 | GRCh38.p7 | 17:78814386 | ACCTGTCCCAGGAGG[C/T]AGCTGCACTGACACA | 57602 |
rs760476610 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78823803 | TCCTAGACTATCGAC[A/C]CTTCTGCTGCCAGAG | 57602 |
rs760513772 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788804 | TCAGCCACTGCCTGA[C/T]GTCATTCCCCTCCAC | 57602 |
rs760540747 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824836 | AGTGACAGCAAGGGG[C/T]CGGCGGAAACCCTGC | 57602 |
rs760546023 | snp | C/T | 1.65649e-05 | 0.00287788 | intron-variant | USP36 | GRCh38.p7 | 17:78799617 | CACCCTTCCCTCCTA[C/T]AAAACCAACCAATGA | 57602 |
rs760588262 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821947 | CTTACCGCGTGATCT[A/G]AGATACCCTCCAAAA | 57602 |
rs760609215 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798428 | GGCACAGTCAGCGGC[A/G]ATAGCTGAGGCTGGC | 57602 |
rs760640809 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78790986 | TGAAAACACGCATGC[-/A]AAGACATGTATCGTG | 57602 |
rs760642104 | snp | C/T | 6.59011e-05 | 0.00573988 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836124 | ACCCTGTCTCCTGGC[C/T]GGTGGGTCATCTCCA | 57602 |
rs760702357 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787720 | CTTTCCATACTGTTA[C/T]GGGTTGAGTCATGTC | 57602 |
rs760711915 | snp | C/T | 5.13668e-05 | 0.00506762 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803762 | AAAGGTCTTTTTCCT[C/T]TTCTCAGAGGGGCTC | 57602 |
rs760755596 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839434 | GATCTCAGAATAAAA[G/T]CCATCTACAAAGTGA | 57602 |
rs760785726 | snp | A/G | 3.75305e-05 | 0.00433172 | intron-variant | USP36 | GRCh38.p7 | 17:78829025 | GCCGGCGTGGAAGGA[A/G]GAGCAATTTTAAGAC | 57602 |
rs760804711 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795946 | CATTTACTTACATAC[A/G]TGTACAAGACCTAGA | 57602 |
rs760822852 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796102 | CTGCCCAAGAGTTAA[C/T]GAATGTATGTACCCC | 57602 |
rs760823455 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805659 | CATGCACAGGGAAGG[G/T]GCTGCATCTCTGGCA | 57602 |
rs760833835 | in-del | -/AA | 1.96643e-05 | 0.00313557 | intron-variant | USP36 | GRCh38.p7 | 17:78827350 | TGTCGGGCGATCTCT[-/AA]AAGAGGAAGAAACAG | 57602 |
rs760846510 | snp | A/G | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806209 | GTGAGAGGTTTTCAT[A/G]GGGTGGGTGAGGTCG | 57602 |
rs760871640 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819978 | ACATCTGCTTTCACA[A/G]AAAGTTCCAGAGCAC | 57602 |
rs760887167 | in-del | -/ACAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815931 | CGCACACATACACAC[-/ACAT]ACATATACACACATG | 57602 |
rs760898043 | snp | C/T | 1.66991e-05 | 0.00288951 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835293 | ACAGCTGCGAGCATG[C/T]TCCTTGGAGAGCAGG | 57602 |
rs760903725 | snp | C/G | 6.58979e-05 | 0.00573974 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812954 | GGAAGGGAGGAGGAG[C/G]CTGTCCTGGAGATGA | 57602 |
rs760926082 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800403 | GTCCACCCAGCACCT[C/T]GGGACCAGGACAGCA | 57602 |
rs760958309 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816744 | AGCCTCCCTAAGTGC[G/T]GACATTAGAGTTGTG | 57602 |
rs760965899 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797072 | GCCACAGGACTGGTC[-/A]AAAAATAAATGTTTT | 57602 |
rs761059468 | snp | C/G | 3.45024e-05 | 0.00415331 | intron-variant | USP36 | GRCh38.p7 | 17:78820940 | GGGTTCTGTTTCACC[C/G]TCTGGCCTCGCTCTC | 57602 |
rs761094465 | snp | A/T | 1.64852e-05 | 0.00287094 | intron-variant | USP36 | GRCh38.p7 | 17:78798895 | AGCCTGTGGTCAGCA[A/T]CACACATCATACCTT | 57602 |
rs761156888 | snp | G/T | 1.65168e-05 | 0.00287369 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836341 | GGTTTCAGGGCCTCC[G/T]TCAACTTATCCACTA | 57602 |
rs761164587 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834190 | AGGCGGAGGTTGCAG[C/T]GAACTGAGATCACAC | 57602 |
rs761173229 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802682 | ATTCTTCCCCCCACA[C/T]GCATTAGCGGACGCT | 57602 |
rs761188351 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826851 | CTGCAGAGACCTCAT[C/T]CCTACCACCCCAACC | 57602 |
rs761253773 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823575 | GGGCAGGAGGTGGCC[C/T]GAGAGCCACCCGGAA | 57602 |
rs761290189 | snp | G/T | 0.00119078 | 0.0243715 | intron-variant | USP36 | GRCh38.p7 | 17:78827083 | GCAATCCCCTATTTG[G/T]GCTCCAACAGTTTGA | 57602 |
rs761325688 | snp | A/G | 1.6574e-05 | 0.00287867 | intron-variant | USP36 | GRCh38.p7 | 17:78798570 | GACCAAGAATCACAG[A/G]CATCACAGTTCCCAA | 57602 |
rs761361994 | snp | G/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841623 | ATCTGAGGCAACTTC[G/T]CTGGCTTCCTCCCCA | 57602 |
rs761430638 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78799294 | CCCTCGTCTGAGGAA[C/G]AAAGATGTCATGTTT | 57602 |
rs761435683 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841070 | GCCGCGGCAGGGTGA[C/T]GTCTCCGCAGCGCAC | 57602 |
rs761447025 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836191 | AGCAACACATATTTG[C/T]TCTTTAAGGCCTCCA | 57602 |
rs761448836 | in-del | -/GGGG | 0.000887726 | 0.0210493 | intron-variant | USP36 | GRCh38.p7 | 17:78827222 | TCCAAAGCCCTGGGA[-/GGGG]GGGTGGGTGGGGAAG | 57602 |
rs761477663 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78799416 | AGACACAGCATGTGT[-/G]GGGCTCCTCACCCTG | 57602 |
rs761555336 | snp | C/T | 6.59304e-05 | 0.00574116 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814489 | AGAGTCCATACATGA[C/T]AGGATCACCATTATT | 57602 |
rs761567636 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816572 | CAGATATTGCAGTGA[C/G]CTGAGATGGTGCCAC | 57602 |
rs761599624 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807091 | ACTTGGCGGCGTTTT[A/G]GAGTGGCCAGCGGTG | 57602 |
rs761608387 | snp | C/T | 0.000132188 | 0.00812874 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807462 | CAGGGTCGTCTAGGA[C/T]GGTTGGCATGTGTGT | 57602 |
rs761671153 | snp | A/C | 0.000133505 | 0.00816913 | intron-variant | USP36 | GRCh38.p7 | 17:78802273 | TGCGGTCCCCCAACC[A/C]CTCGCCCGGTGCACA | 57602 |
rs761710863 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842733 | TCCCAGGCAGGGAGC[A/G]GACCAGGTAATTTTT | 57602 |
rs761714667 | snp | A/C | 3.31565e-05 | 0.0040715 | intron-variant | USP36 | GRCh38.p7 | 17:78814400 | GCAGCTGCACTGACA[A/C]AAGCCTCTCACCTTC | 57602 |
rs761731693 | snp | C/T | 0.000148399 | 0.00861262 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814521 | TGGGACATATACGGA[C/T]GTATGTTGAGGAATT | 57602 |
rs761743296 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822942 | CAGGCTCTCCAGCCC[C/T]GTCTCCCCAGCTGCT | 57602 |
rs761775479 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807940 | AACTTCTGGCCTCGA[A/G]CAGTCCACCTGCCTC | 57602 |
rs761779528 | snp | A/G | 1.71416e-05 | 0.00292755 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803814 | GGCAACTGGTGTGGA[A/G]GAGACACAAGGTCCT | 57602 |
rs761780268 | snp | A/C | 4.97723e-05 | 0.00498835 | intron-variant | USP36 | GRCh38.p7 | 17:78827217 | AAGGTGTCCAAAGCC[A/C]TGGGAGGGTGGGTGG | 57602 |
rs761792139 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78804626 | TGATCCCTGAGATTT[-/A]AAAAAAAAAAAAAAA | 57602 |
rs761865292 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808785 | GCTTGACCAAGAGGC[C/T]GTACCCGTTATCTCT | 57602 |
rs761902317 | snp | A/T | 1.65168e-05 | 0.00287369 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799711 | TATTTGAGCAGTTCC[A/T]GGACCACATCAGACT | 57602 |
rs761930763 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837021 | GAAGAGAAATACTCA[C/G]TAGTATAAGAAGAGA | 57602 |
rs761954425 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812963 | GAGGAGCCTGTCCTG[C/G]AGATGAGGCCCTCGG | 57602 |
rs761964104 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78814238 | GATTCTGGTGCAACA[A/C]TTCTGTAAAGGGCAT | 57602 |
rs761988837 | snp | A/C | 1.65124e-05 | 0.00287331 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803583 | CTCCTGTACATGGGG[A/C]TCCCAGGCTGTCTCT | 57602 |
rs762018389 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827689 | GGGAGGATCACTTGA[G/T]CCCAGGAGTTCGAGG | 57602 |
rs762019942 | snp | A/G/T | 5.07879e-05 | 0.00503903 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827286 | CTGCATGGCGTCGAT[A/G/T]GTGTACCGCAGGAAC | 57602 |
rs762023456 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793607 | CCCGTCTGCATGTCA[C/T]GTGACCTGTCCACAC | 57602 |
rs762044682 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78819780 | TTCGTGTTATTTAGA[A/C]GTTTGAGTTTTTAGG | 57602 |
rs762258013 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811012 | ACAGCTACTCAGGAG[A/G]CAGAGGCAGGAGAAT | 57602 |
rs762262292 | snp | A/G | 0.000133089 | 0.00815641 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807262 | GTTCCCCTTCAGCCC[A/G]TGCCCGTTGGCAGTG | 57602 |
rs762265490 | snp | C/T | 3.33317e-05 | 0.00408224 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807219 | TGGAGCTGCTGGAGC[C/T]CCTCCTGTCGAGGCC | 57602 |
rs762291829 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798955 | CAACCACGGTCTCAG[G/T]CCGGGCCTGTCTGCT | 57602 |
rs762299298 | snp | A/G | 2.01161e-05 | 0.00317138 | intron-variant | USP36 | GRCh38.p7 | 17:78827353 | CGGGCGATCTCTAAA[A/G]GAGGAAGAAACAGGG | 57602 |
rs762349507 | snp | A/T | 1.64925e-05 | 0.00287158 | intron-variant | USP36 | GRCh38.p7 | 17:78798901 | TGGTCAGCATCACAC[A/T]TCATACCTTCCCTCG | 57602 |
rs762375829 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814504 | CAGGATCACCATTAT[C/T]CTGGGACATATACGG | 57602 |
rs762387994 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805708 | CGAGAGCCCTGAGAC[A/G]GTTCTTAACCTGCAT | 57602 |
rs762395340 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820542 | CACTTTTATCAGGAT[G/T]ATCTTGTAGCTGGAC | 57602 |
rs762402424 | snp | A/T | 5.23501e-05 | 0.00511589 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803881 | AGCTCCGTGGTTCTG[A/T]CGTCCCTGGGGGCTT | 57602 |
rs762478984 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825301 | CGCTCTGATCATAAT[C/G]CAAGTAACATCAAAA | 57602 |
rs762510213 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791325 | TTTTAGTAGAGACGG[C/G]GTTTCTCCATGTTGT | 57602 |
rs762518928 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825874 | CAGGCCCTCGGGGGT[C/T]ACTTCTCCCAGGAAG | 57602 |
rs762568910 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833691 | TTCTACTTAGAGATT[C/T]TCTGCGATGAAAACA | 57602 |
rs762593172 | snp | A/C/G | 4.94216e-05 | 0.00497079 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812946 | GGCGGCCGGGAAGGG[A/C/G]GGAGGAGCCTGTCCT | 57602 |
rs762617658 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800327 | GGCTGCTGCCATCAG[A/G]GGCCCGACCTCCTAA | 57602 |
rs762648889 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823856 | ACTGCACGGGGCAGA[C/T]AGAGGAGGCGCTCTG | 57602 |
rs762666876 | snp | A/G | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807138 | GAGAATCGCAGAGAT[A/G]GGCCGCTCCACTCCT | 57602 |
rs762672082 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836229 | GGAGAAGCTCTTGCT[A/G]GCTGGCTCGAACTCG | 57602 |
rs762683755 | snp | C/T | 1.82317e-05 | 0.00301919 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807605 | ATCTCTTCAGTGGTG[C/T]GCGGCTTCTTCATCG | 57602 |
rs762716031 | snp | C/T | 1.72024e-05 | 0.00293273 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803819 | CTGGTGTGGAAGAGA[C/T]ACAAGGTCCTCGTTG | 57602 |
rs762770604 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839798 | TTCCTGTAATCACTA[A/G]CAATCCCTCCGACGC | 57602 |
rs762783543 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796412 | ATTCAGAGACTGGTC[C/T]GCAGGAGAGGGCACC | 57602 |
rs762790067 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832216 | TAGCTAAATATTAGC[A/G]CCAGAGACAGTCCAG | 57602 |
rs762926146 | snp | A/C/T | 0.00011951 | 0.00772921 | intron-variant | USP36 | GRCh38.p7 | 17:78802276 | GGTCCCCCAACCCCT[A/C/T]GCCCGGTGCACACCC | 57602 |
rs762988968 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78791130 | CCCAATCTGGCCTTC[-/TTTTTTTTTTTTT]TTTTTTTTTTAGCTG | 57602 |
rs762990745 | snp | C/T | 1.6669e-05 | 0.00288691 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807521 | GACCCCGAGGGCAGC[C/T]TTGGAGGAATGCAGC | 57602 |
rs762995545 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78821740 | ACCACACCCAGCCCT[C/T]GTGGGAATATTCTAA | 57602 |
rs763015564 | snp | C/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807141 | AATCGCAGAGATGGG[C/T]CGCTCCACTCCTGGG | 57602 |
rs763037682 | snp | A/G/T | 3.29626e-05 | 0.00405961 | intron-variant | USP36 | GRCh38.p7 | 17:78821917 | TGGCAAGAAGCAGTA[A/G/T]AACAAACGTCTCCAC | 57602 |
rs763042073 | snp | C/T | 6.2315e-05 | 0.00558154 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802335 | ATACCCATGCGGTCC[C/T]CAGGACACCAGCCAT | 57602 |
rs763056095 | snp | A/G | 9.88338e-05 | 0.00702902 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798958 | CCACGGTCTCAGTCC[A/G]GGCCTGTCTGCTGTC | 57602 |
rs763073744 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78832063 | TAAGTGGCACATGGA[A/C]AAATATTTATTCATG | 57602 |
rs763074109 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814039 | AATATTTTCATAACT[C/T]GGAATGTGACCCCAA | 57602 |
rs763087148 | snp | A/G/T | 4.95359e-05 | 0.00497653 | intron-variant | USP36 | GRCh38.p7 | 17:78813736 | AAGAAAAGAGCAGAG[A/G/T]GAGTGAGCTCATCTG | 57602 |
rs763096581 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807002 | GCTGGTGGAGGAGAC[A/G]TGGTGCTTGCAGGCT | 57602 |
rs763096707 | snp | C/T | 3.32535e-05 | 0.00407746 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803620 | GCCCCTCCTGCAGGG[C/T]GCTGGCAGCTGTGTC | 57602 |
rs763140376 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813790 | CAGATAGAACAGCAC[A/G]TAGGCCTGCTGGTTC | 57602 |
rs763218568 | snp | A/G | 5.16747e-05 | 0.00508278 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803672 | CCTCTTCCTCTTCCC[A/G]TGGGGAGCCGCAGTG | 57602 |
rs763229785 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835484 | CGTCACCACAGCTCT[C/T]ATACGTGTGCTCACT | 57602 |
rs763256558 | in-del | -/TATA | | | intron-variant | USP36 | GRCh38.p7 | 17:78834999 | AAAATAATATTTGTA[-/TATA]TATATATATATATAT | 57602 |
rs763320322 | snp | G/T | 3.30186e-05 | 0.00406303 | intron-variant | USP36 | GRCh38.p7 | 17:78818792 | ATCTATGAAGAAGGT[G/T]ATGAGAAAGATTAAT | 57602 |
rs763390617 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805351 | CAAATCTTATGCTAG[G/T]TATAGGGCAGAGGTG | 57602 |
rs763408313 | snp | C/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806190 | AAGTGGAGGCAACGA[C/T]GGGGTGAGAGGTTTT | 57602 |
rs763430031 | snp | A/C | 1.64773e-05 | 0.00287026 | intron-variant | USP36 | GRCh38.p7 | 17:78827369 | GAGGAAGAAACAGGG[A/C]GGGAAGAGCTCGTGT | 57602 |
rs763515271 | in-del | -/GTGCTCT | 1.66258e-05 | 0.00288316 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807193 | GTCGCTGCTGGCCGA[-/GTGCTCT]GGGCTGGAGCTGCTG | 57602 |
rs763530817 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811118 | CCTCAGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 57602 |
rs763575675 | in-del | -/AC | 1.96165e-05 | 0.00313175 | intron-variant | USP36 | GRCh38.p7 | 17:78807658 | AGACCAAAGCAGAAA[-/AC]ACAACTGAGGAAGCG | 57602 |
rs763626403 | snp | C/G | 9.88435e-05 | 0.00702937 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807039 | TGGTGTTGCTCAGGA[C/G]AGGGGACTTCAGCTT | 57602 |
rs763628376 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815870 | ATGCATACACATGTA[C/T]GCATATACATACATG | 57602 |
rs763643610 | in-del | -/C | 3.54717e-05 | 0.00421125 | intron-variant | USP36 | GRCh38.p7 | 17:78803358 | CTCGTCAGAGGTAGA[-/C]AGATGCCACTTTGCT | 57602 |
rs763714583 | snp | A/G | 4.25777e-05 | 0.00461379 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835456 | AAAAGCACTTTCTGC[A/G]GGGCTGGGACTCCGT | 57602 |
rs763715224 | snp | C/T | 5.1424e-05 | 0.00507044 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803712 | ATGTGCTGTGGGAGG[C/T]GCGTCTCTGAGCCCA | 57602 |
rs763717745 | snp | C/T | 3.76046e-05 | 0.004336 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802446 | TCCTCTTCTACTGCC[C/T]GCTGTGTCTCCTGCT | 57602 |
rs763743290 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | USP36 | GRCh38.p7 | 17:78799625 | CCTCCTACAAAACCA[A/G]CCAATGAAAGGCAAA | 57602 |
rs763755761 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839814 | CAATCCCTCCGACGC[A/G]CACACCATCCACACT | 57602 |
rs763802264 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841528 | CTCCAAAAGCTTTGT[C/T]CTCTGACAGCTCTGC | 57602 |
rs763859717 | snp | C/T | 1.85317e-05 | 0.00304393 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807619 | GTGCGGCTTCTTCAT[C/T]GTCCCAGAGTCTTGT | 57602 |
rs763883326 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830028 | ACAGGCGTGAGCCAT[C/T]GAGCCCAGCCCCGAC | 57602 |
rs763904977 | snp | A/C | 1.7146e-05 | 0.00292792 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803770 | TTTTCCTCTTCTCAG[A/C]GGGGCTCTGGGGGGG | 57602 |
rs763957123 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797235 | TGTATTCGCAGGTAT[C/T]GAGGGCTCCTCCGAC | 57602 |
rs763957544 | snp | C/G | 1.6513e-05 | 0.00287336 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799701 | ATCAGATGAGTATTT[C/G]AGCAGTTCCTGGACC | 57602 |
rs763973216 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821965 | ATACCCTCCAAAAAT[C/T]TGATGGACCAAGGTA | 57602 |
rs764019486 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806250 | AGGGGGGAGGTGGAC[A/G]GAGGTCATTGCCGGT | 57602 |
rs764026254 | snp | A/G | 0.000285185 | 0.0119378 | intron-variant | USP36 | GRCh38.p7 | 17:78827040 | CAGCAGGACGTCTCC[A/G]GAGACAGCCCTTTCC | 57602 |
rs764080745 | snp | A/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819984 | GCTTTCACAAAAAGT[A/T]CCAGAGCACGCACAA | 57602 |
rs764090613 | snp | A/G | 4.95651e-05 | 0.00497796 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807143 | TCGCAGAGATGGGCC[A/G]CTCCACTCCTGGGGG | 57602 |
rs764104793 | in-del | -/CAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78798304 | TACACAGCCCACATA[-/CAT]CATACACACACGCCA | 57602 |
rs764116222 | snp | A/C | 4.9423e-05 | 0.00497082 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812921 | TTGGAGTGATCTGGA[A/C]TCACACTCGGGCGGC | 57602 |
rs764135680 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78799126 | TACTCATAATTAGTC[A/C]ACAATTTTGAGTGCC | 57602 |
rs764186660 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807895 | TTTTGACAGAGATGG[A/G]GTTTCACCATGTTGG | 57602 |
rs764209207 | snp | A/G | 1.75782e-05 | 0.00296459 | intron-variant | USP36 | GRCh38.p7 | 17:78803366 | AGGTAGACAGATGCC[A/G]CTTTGCTCCTGCCCT | 57602 |
rs764253415 | snp | C/T | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807456 | TCTTTCCAGGGTCGT[C/T]TAGGATGGTTGGCAT | 57602 |
rs764287211 | snp | C/T | 3.42894e-05 | 0.00414048 | intron-variant | USP36 | GRCh38.p7 | 17:78820943 | TTCTGTTTCACCCTC[C/T]GGCCTCGCTCTCCTA | 57602 |
rs764287915 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814169 | CCAGGGTTCTAAGGA[A/T]GGCACCAGAAGCGGC | 57602 |
rs764331946 | snp | G/T | 1.64944e-05 | 0.00287175 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803471 | CCTGCTGCTCGCGTG[G/T]TGGCCGTCCGTAACA | 57602 |
rs764353668 | in-del | -/C | 1.64776e-05 | 0.00287028 | intron-variant | USP36 | GRCh38.p7 | 17:78827368 | GAGGAAGAAACAGGG[-/C]AGGGAAGAGCTCGTG | 57602 |
rs764359530 | snp | A/G | 3.30524e-05 | 0.00406511 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836345 | TCAGGGCCTCCTTCA[A/G]CTTATCCACTATTGG | 57602 |
rs764404049 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806210 | TGAGAGGTTTTCATG[C/G]GGTGGGTGAGGTCGG | 57602 |
rs764427783 | snp | G/T | 1.93932e-05 | 0.00311387 | intron-variant | USP36 | GRCh38.p7 | 17:78829035 | AAGGAGGAGCAATTT[G/T]AAGACAAGAGCTTTC | 57602 |
rs764443005 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78803049 | GCTCAAACCATCCTC[C/T]CACCTCAGCCTCCTG | 57602 |
rs764462185 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78808863 | AGTCGGTGCTTAAAA[A/C]ATATTTGTTGAGCTT | 57602 |
rs764462668 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835575 | TCCACAAAAAGAAAC[C/T]CCTGAAGCATACACT | 57602 |
rs764488350 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819602 | CTCGTGCTCTGCCAC[A/G]TCCTCTTGGTGTGGC | 57602 |
rs764499143 | snp | C/T | 0.0001227 | 0.00783168 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803888 | TGGTTCTGACGTCCC[C/T]GGGGGCTTGGGGGTA | 57602 |
rs764512016 | snp | A/G | 0.000700967 | 0.0187081 | intron-variant | USP36 | GRCh38.p7 | 17:78827222 | GTCCAAAGCCCTGGG[A/G]GGGTGGGTGGGGAAG | 57602 |
rs764517917 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | USP36 | GRCh38.p7 | 17:78798896 | GCCTGTGGTCAGCAT[C/G]ACACATCATACCTTC | 57602 |
rs764603428 | snp | C/T | 6.60939e-05 | 0.00574827 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807142 | ATCGCAGAGATGGGC[C/T]GCTCCACTCCTGGGG | 57602 |
rs764679451 | snp | C/T | 1.65754e-05 | 0.00287879 | intron-variant | USP36 | GRCh38.p7 | 17:78798571 | ACCAAGAATCACAGG[C/T]ATCACAGTTCCCAAA | 57602 |
rs764702182 | snp | C/G/T | 0.000159387 | 0.00892592 | intron-variant | USP36 | GRCh38.p7 | 17:78827218 | AGGTGTCCAAAGCCC[C/G/T]GGGAGGGTGGGTGGG | 57602 |
rs764744735 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793503 | GGGGCCAAGCCAAGG[C/T]GGGATCTGCACGAAG | 57602 |
rs764799075 | snp | G/T | 8.73362e-05 | 0.00660761 | intron-variant | USP36 | GRCh38.p7 | 17:78827084 | CAATCCCCTATTTGG[G/T]CTCCAACAGTTTGAG | 57602 |
rs764801846 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799547 | TTCCTCTTCCCATTC[G/T]CAAAGCCGAGCGATG | 57602 |
rs764829799 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815229 | TCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 57602 |
rs764838049 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809643 | CTTTGTTTTTCTGGG[A/G]TTTTTTGAGACAGGG | 57602 |
rs764856473 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798460 | GCCTTTGCTGGGTGA[A/G]TCACAGACCAGAAGT | 57602 |
rs764865721 | in-del | -/CT | | | intron-variant | USP36 | GRCh38.p7 | 17:78818051 | GATTATGCCACTGCA[-/CT]CCAGCCCAGGTGACA | 57602 |
rs764910341 | snp | C/T | 6.60513e-05 | 0.00574641 | intron-variant | USP36 | GRCh38.p7 | 17:78799647 | AAAGGCAAACAGAAG[C/T]CCTGTCTCCAAATCA | 57602 |
rs764910425 | snp | A/G | 1.64982e-05 | 0.00287208 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803815 | GCAACTGGTGTGGAA[A/G]AGACACAAGGTCCTC | 57602 |
rs764955497 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825193 | AGTCTCAGCAGCCAC[C/T]GCCAAGCATGCAGGA | 57602 |
rs765001673 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833629 | GAAGCAAACCCTACA[C/G]GCCAGGCTCCTGAGC | 57602 |
rs765007600 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816291 | CTACCTCCCAAGTAG[C/T]TGGGACTATAGGCAC | 57602 |
rs765033910 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78790174 | GCTCACTGCAACCTC[A/G]GCTTTCCAGGTTCAA | 57602 |
rs765076639 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806254 | GGGAGGTGGACGGAG[A/G]TCATTGCCGGTCGCC | 57602 |
rs765078399 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814715 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGGGGA | 57602 |
rs765086008 | snp | A/C | 1.90776e-05 | 0.00308844 | intron-variant | USP36 | GRCh38.p7 | 17:78802274 | GCGGTCCCCCAACCC[A/C]TCGCCCGGTGCACAC | 57602 |
rs765109682 | snp | A/T | 3.29641e-05 | 0.00405968 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814493 | TCCATACATGACAGG[A/T]TCACCATTATTCTGG | 57602 |
rs765182743 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78830507 | TGGGTCAGTTTCTCT[A/C]AAGTACACGCTCAGA | 57602 |
rs765215511 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839570 | GAACCACTTAGGGAG[A/G]GGATAAACGAACCTT | 57602 |
rs765239652 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815842 | ACATATATACATACA[C/T]ACACACATATGCATG | 57602 |
rs765247353 | snp | C/G | 1.65176e-05 | 0.00287376 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799712 | ATTTGAGCAGTTCCT[C/G]GACCACATCAGACTC | 57602 |
rs765281175 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807168 | TGGGGGTCTGGGGGG[C/T]CTTGGTGGAGTCGCT | 57602 |
rs765308413 | snp | A/C | 4.9783e-05 | 0.00498889 | intron-variant | USP36 | GRCh38.p7 | 17:78798582 | CAGGCATCACAGTTC[A/C]CAAAAACGGCTCTTT | 57602 |
rs765333570 | in-del | -/CTAT | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837681 | CAAACACAGCACAGA[-/CTAT]CTGAGTCACAATTTC | 57602 |
rs765394816 | snp | A/G | 2.38695e-05 | 0.00345459 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821026 | CCAAGTAGGGGTCGT[A/G]GGTGTCCGAGACGCT | 57602 |
rs765403001 | snp | A/C | 6.59207e-05 | 0.00574073 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812969 | CCTGTCCTGGAGATG[A/C]GGCCCTCGGGACTTT | 57602 |
rs765450962 | snp | C/T | 4.96028e-05 | 0.00497985 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835317 | GAGCAGGTAGTTGGC[C/T]AGAGGTGGTGTGTAG | 57602 |
rs765459096 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796267 | ACATGGCAGAGGGAA[C/T]AGTTCACACAGGAAT | 57602 |
rs765471675 | snp | A/G | 4.94654e-05 | 0.00497295 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803481 | GCGTGGTGGCCGTCC[A/G]TAACACATCCCACCT | 57602 |
rs765509578 | snp | A/G | 0.000164761 | 0.00907487 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819994 | AAAGTTCCAGAGCAC[A/G]CACAATATTCGCAGC | 57602 |
rs765515561 | snp | A/G | 2.12836e-05 | 0.00326211 | intron-variant | USP36 | GRCh38.p7 | 17:78827365 | AAAAGAGGAAGAAAC[A/G]GGGAGGGAAGAGCTC | 57602 |
rs765523734 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792590 | AATCAGAATGCGGGG[G/T]AAGGAGCCCGGCAAC | 57602 |
rs765562791 | snp | A/G | 0.000279672 | 0.0118219 | intron-variant | USP36 | GRCh38.p7 | 17:78820964 | CGCTCTCCTACTGCA[A/G]AAGTGAAGGGCAGGA | 57602 |
rs765570767 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818708 | TGGCAAAGCGCTTGA[G/T]GGAAAGGGTTAAGAC | 57602 |
rs765576387 | snp | A/G | 1.84742e-05 | 0.0030392 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803948 | GGGGGGTTGCAGGCG[A/G]CTGGATGATTGGGGA | 57602 |
rs765590892 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | USP36 | GRCh38.p7 | 17:78806127 | GGGAGAACCAGTTGG[C/T]ACCCAGAAGATCCCG | 57602 |
rs765590936 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78838518 | TCTCACCAACTGAAC[A/C]ATCACTGCTGCGTCA | 57602 |
rs765596353 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787450 | ATAAGTGAAAAAAGC[A/T]GTCAGAACGGTGGTA | 57602 |
rs765615467 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78835552 | GACGTAAGTCCACAC[A/G]CAGGTCGTCCACAAA | 57602 |
rs765625352 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811269 | AGTTCTAGCAGAAAA[C/T]TTCAAATACACACAA | 57602 |
rs765696480 | snp | G/T | 1.65589e-05 | 0.00287736 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836360 | ACTTATCCACTATTG[G/T]CATGGTGCATCACTG | 57602 |
rs765761723 | snp | A/C | 3.51037e-05 | 0.00418935 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803894 | TGACGTCCCTGGGGG[A/C]TTGGGGGTACTGGAC | 57602 |
rs765805295 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802799 | GCTACTGTGACCTGA[C/T]GAAACGGCAGATCCT | 57602 |
rs765854907 | snp | C/T | 5.23647e-05 | 0.0051166 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803882 | GCTCCGTGGTTCTGA[C/T]GTCCCTGGGGGCTTG | 57602 |
rs765859227 | snp | A/G | 1.65531e-05 | 0.00287686 | intron-variant | USP36 | GRCh38.p7 | 17:78818621 | TGTTATTCTGATGCC[A/G]ACTGTGGCCCACGGA | 57602 |
rs765872960 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805718 | GAGACAGTTCTTAAC[C/T]TGCATGACGCTAGCA | 57602 |
rs765901154 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78818528 | AGTCCCTACTTCACA[A/T]TATGTGTAGAACCTT | 57602 |
rs765912155 | snp | C/G | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814507 | GATCACCATTATTCT[C/G]GGACATATACGGACG | 57602 |
rs765918116 | snp | A/C | 1.72389e-05 | 0.00293584 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803827 | GAAGAGACACAAGGT[A/C]CTCGTTGACCTGAGG | 57602 |
rs765920577 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78798288 | ACACACATGTGCCAG[A/T]TACACAGCCCACATA | 57602 |
rs765963626 | snp | C/T | 3.3066e-05 | 0.00406595 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807471 | CTAGGATGGTTGGCA[C/T]GTGTGTGGGTGTCTG | 57602 |
rs765985735 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78832303 | AACACCCCTTAGGAT[A/C]CTCAACTCTTCAAAT | 57602 |
rs766079613 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836231 | AGAAGCTCTTGCTGG[C/T]TGGCTCGAACTCGAT | 57602 |
rs766093944 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832908 | AATCTCAGCACTTTC[A/G]GAGGCAGAGGCAGGC | 57602 |
rs766105638 | snp | A/G | 1.69476e-05 | 0.00291093 | intron-variant | USP36 | GRCh38.p7 | 17:78806931 | GCTCTCCTGATACAC[A/G]GCAGCGGCGAGACCC | 57602 |
rs766106625 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823838 | AGCCAACCATGAAAG[C/T]GCACTGCACGGGGCA | 57602 |
rs766117171 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78808794 | AGAGGCTGTACCCGT[C/T]ATCTCTCTCGTTCCC | 57602 |
rs766191532 | snp | C/G | 1.73192e-05 | 0.00294267 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835431 | CCTCAGAGACAGTCG[C/G]TCCGTGGGGAAAAGC | 57602 |
rs766191780 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815934 | CACACATACACACAC[-/AT]ATACACACATGCATG | 57602 |
rs766192806 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832383 | CTCAGGATCCAGTGG[A/G]GTGCAGGAAAAAAAG | 57602 |
rs766218491 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796350 | TGCTTTCCCTTCCAG[A/G]TAAGTTACAAAGCCA | 57602 |
rs766239544 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835356 | CTGGATGGTGGCATT[A/G]AGAAAGCAGGTGTTG | 57602 |
rs766262084 | snp | A/G | 1.67136e-05 | 0.00289076 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807527 | GAGGGCAGCTTTGGA[A/G]GAATGCAGCCGTTCT | 57602 |
rs766295898 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78838511 | AAAGACTTCTCACCA[A/T]CTGAACAATCACTGC | 57602 |
rs766296821 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815141 | GATTGAGACCATCGT[A/G]GCCAAGATGGCGAAA | 57602 |
rs766322884 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815220 | GCCTGTAGTTCCAGC[A/T]ACTCAGGAGGCTGAG | 57602 |
rs766329339 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798961 | CGGTCTCAGTCCGGG[A/C]CTGTCTGCTGTCTTC | 57602 |
rs766378786 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78787757 | AAAGATATGTTGAAG[C/T]CCTAAGCCCCAGTAC | 57602 |
rs766431336 | snp | A/G | 3.77972e-05 | 0.00434709 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803967 | GATGATTGGGGAGCA[A/G]GTGACACAGCCCTGT | 57602 |
rs766502659 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813793 | ATAGAACAGCACGTA[A/G]GCCTGCTGGTTCAGA | 57602 |
rs766548322 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793799 | TAGGGATAAACAGAT[A/G]CCCACCTGATTCCCC | 57602 |
rs766566497 | snp | A/T | 1.72113e-05 | 0.00293348 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803673 | CTCTTCCTCTTCCCG[A/T]GGGGAGCCGCAGTGG | 57602 |
rs766623192 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811157 | AAAAAAAAAAAAAAG[A/G]AACAGTCATCAAGAG | 57602 |
rs766627365 | snp | A/G | 0.000133176 | 0.00815905 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807268 | CTTCAGCCCATGCCC[A/G]TTGGCAGTGGCTGTA | 57602 |
rs766639828 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794558 | CTGCCCGCCGCCTGC[A/G]AGACGACGTGAGTGT | 57602 |
rs766643196 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829427 | CTAAAATATTTTAGG[A/G]CTGACAGCCCCTTAG | 57602 |
rs766657162 | snp | C/T | 0.0001073 | 0.00732383 | intron-variant | USP36 | GRCh38.p7 | 17:78803345 | TTTTGCTTTGTTTCT[C/T]GTCAGAGGTAGACAG | 57602 |
rs766661088 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78802709 | CGCTCCACACGCAGC[A/C]ACGGAGACAGTAGAG | 57602 |
rs766718734 | snp | C/T | 1.88784e-05 | 0.00307227 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802448 | CTCTTCTACTGCCCG[C/T]TGTGTCTCCTGCTTT | 57602 |
rs766733950 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | USP36 | GRCh38.p7 | 17:78798395 | CCCACCCCCTCGGAA[C/T]CGACCTCCTTCCACA | 57602 |
rs766736159 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833742 | CATAAGTTGCTTACA[A/G]TTTTTTAGAAACTGT | 57602 |
rs766763515 | snp | A/G | 1.86461e-05 | 0.00305331 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807625 | CTTCTTCATCGTCCC[A/G]GAGTCTTGTCGCTAA | 57602 |
rs766793450 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823902 | AACCAGCCGACCCAC[A/G]AGATAAATGAAAGCA | 57602 |
rs766875006 | snp | C/T | 3.30011e-05 | 0.00406195 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828921 | CTCGGATGAAGGAGA[C/T]GGGCTTGATGGCGTT | 57602 |
rs766879827 | in-del | -/TC | 1.65312e-05 | 0.00287495 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803594 | GGGGCTCCCAGGCTG[-/TC]TCTGTGTCTGCCCCT | 57602 |
rs766928228 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834441 | CCAGCTAATTGTTTC[A/G]ATTTGTTTTTTGTGT | 57602 |
rs766994027 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791228 | CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 57602 |
rs767000837 | snp | C/T | 4.86393e-05 | 0.00493126 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802352 | AGGACACCAGCCATT[C/T]GCGGATGGTGCGCAG | 57602 |
rs767032132 | in-del | -/TTT | 0.000135269 | 0.00822291 | cds-indel, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802465 | GTGTCTCCTGCTTTC[-/TTT]TTTTCTTTTTCTTTT | 57602 |
rs767034627 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826879 | ACCTCTTTTCAAAAA[C/T]GACATGATTTTTAAG | 57602 |
rs767040176 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842736 | CAGGCAGGGAGCGGA[C/T]CAGGTAATTTTTGGG | 57602 |
rs767041311 | in-del | -/GAG | 1.66715e-05 | 0.00288712 | intron-variant | USP36 | GRCh38.p7 | 17:78812811 | TGTGAGGAGGTCTGT[-/GAG]GAGCACCAAGACCAG | 57602 |
rs767068262 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807957 | AGTCCACCTGCCTCA[A/G]CCTCCAGAAGTGTTG | 57602 |
rs767112528 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833431 | GGATTACAGGTGTGA[C/G]CCACCGTGCCCAGCC | 57602 |
rs767121278 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817056 | AGCGATCCCATAAGA[C/T]TATAATACTGCATTT | 57602 |
rs767122376 | snp | A/G | 1.84123e-05 | 0.00303411 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803945 | GAAGGGGGGTTGCAG[A/G]CGGCTGGATGATTGG | 57602 |
rs767146466 | in-del | -/CTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78810670 | ACTTCAATTCTAATG[-/CTT]CTAATTTCAGCTTCT | 57602 |
rs767156870 | snp | A/G | 1.72314e-05 | 0.0029352 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803682 | TTCCCGTGGGGAGCC[A/G]CAGTGGCCTCCCTGA | 57602 |
rs767173195 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797751 | AGCCTCTGTGTTGGG[C/T]GGTCTGTGGACACTG | 57602 |
rs767228172 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832211 | TCTTCTAGCTAAATA[C/T]TAGCGCCAGAGACAG | 57602 |
rs767268618 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817309 | GTTACACGACACCTG[A/G]GTCTACGACATTAAG | 57602 |
rs767288281 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant | USP36 | GRCh38.p7 | 17:78818632 | TGCCGACTGTGGCCC[A/G]CGGAGCTGCCTGGGA | 57602 |
rs767322930 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814241 | TCTGGTGCAACACTT[C/T]TGTAAAGGGCATCTT | 57602 |
rs767367884 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798991 | CAATAGCATCCTGAC[C/T]GACCGCCGACATCTT | 57602 |
rs767370845 | in-del | -/TTTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78800970 | CATGTTAGGGCAGTA[-/TTTTT]TTTTTTTTTTTTTTT | 57602 |
rs767385597 | snp | A/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807020 | GTGCTTGCAGGCTCA[A/G]TGGTGGTGTTGCTCA | 57602 |
rs767399235 | snp | A/G | 6.59055e-05 | 0.00574007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813818 | TTCAGAACCACCTTG[A/G]CGTTGCTGGAATGGA | 57602 |
rs767426729 | snp | C/T | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807381 | TCGAGTTGCTGGTCC[C/T]AGGCAGCCCCTGAGC | 57602 |
rs767443438 | snp | C/G | 0.000132231 | 0.00813008 | intron-variant | USP36 | GRCh38.p7 | 17:78835531 | GACAAGGGAAGAAAA[C/G]AGGAAGACGTAAGTC | 57602 |
rs767525812 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797311 | GGAAGGGGTGCACAG[G/T]AGGGCCACCCTCTCG | 57602 |
rs767645820 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836826 | CACACACAAACGGAC[-/AC]ACACACACACACACC | 57602 |
rs767650056 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | USP36 | GRCh38.p7 | 17:78806151 | GATCCCGGCCCAAAG[C/T]TTACCTGGCTCTATG | 57602 |
rs767681276 | snp | A/G | 1.85896e-05 | 0.00304868 | intron-variant | USP36 | GRCh38.p7 | 17:78829022 | CCTGCCGGCGTGGAA[A/G]GAGGAGCAATTTTAA | 57602 |
rs767690331 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78805562 | CCCAGCGGCTTCCAG[A/C]CAGCCATTTACCAGT | 57602 |
rs767702796 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | USP36 | GRCh38.p7 | 17:78799065 | CGAGTGCAGGTTCCC[A/G]GGTCCCCTGTGGCTT | 57602 |
rs767762659 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806197 | GGCAACGACGGGGTG[A/G]GAGGTTTTCATGGGG | 57602 |
rs767780014 | snp | A/G | 1.65575e-05 | 0.00287724 | intron-variant | USP36 | GRCh38.p7 | 17:78798561 | CTTTTCCTAGACCAA[A/G]AATCACAGGCATCAC | 57602 |
rs767786452 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810842 | CATCCAGGCCGGGCA[C/T]GGTGGCTCATGCCTG | 57602 |
rs767795884 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811570 | CTACTCACATTTTCC[C/G]CGTTAAATGTGAGAA | 57602 |
rs767807281 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812907 | TGCCGATGTTCTTCT[C/T]GGAGTGATCTGGAAT | 57602 |
rs767814555 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807281 | CCGTTGGCAGTGGCT[A/G]TAGCCAGGAGCTTAG | 57602 |
rs767836279 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825798 | TATAGGCTCGCTGCA[C/T]TCCCCCTGCAGGTGC | 57602 |
rs767841412 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792783 | GAGTGCAGTGGCATG[A/G]TCTTGGCTCACTGCA | 57602 |
rs767872502 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78833697 | TTAGAGATTTTCTGC[A/G]ATGAAAACATCCTGC | 57602 |
rs767910205 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828100 | TGGTGCGCCTGTAAT[C/G]CCAGCTACTCAGAAG | 57602 |
rs767912712 | in-del | -/G | 1.64762e-05 | 0.00287016 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812934 | GAATCACACTCGGGC[-/G]GCCGGGAAGGGAGGA | 57602 |
rs767930328 | snp | A/G | 3.30273e-05 | 0.00406356 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807139 | AGAATCGCAGAGATG[A/G]GCCGCTCCACTCCTG | 57602 |
rs767961453 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836143 | GGGTCATCTCCACTC[A/T]TGTGGCGACTAGCTC | 57602 |
rs768036842 | snp | C/T | 8.28562e-05 | 0.00643593 | intron-variant | USP36 | GRCh38.p7 | 17:78812839 | ACCAGCCACTTTGGC[C/T]TCCATCATTCTCACA | 57602 |
rs768118276 | snp | A/G | 7.05293e-05 | 0.00593799 | intron-variant | USP36 | GRCh38.p7 | 17:78802558 | GAAGTGAGAGGCAGC[A/G]GTCAGCTCTGAGCAA | 57602 |
rs768135763 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809797 | CTGGCTAATTTTTGC[A/T]CTTTTTTTGGAGATG | 57602 |
rs768165551 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798430 | CACAGTCAGCGGCGA[C/T]AGCTGAGGCTGGCAG | 57602 |
rs768169484 | snp | A/C | 1.65299e-05 | 0.00287483 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803431 | CTTCTTCACCAAGAC[A/C]TTCTGCTCCTTTCCT | 57602 |
rs768193939 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792722 | GGGAAGGTTTTTTTT[A/G]TTGTCGTTGTTTTTG | 57602 |
rs768244762 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78813521 | ATTTGGGGCAATACT[A/G]TAAATGGTGACTTTC | 57602 |
rs768317431 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812071 | GTGCACTGATAGTCC[C/T]GAATACTAGGGATGC | 57602 |
rs768324333 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836300 | GCTTCCCCAGTTCTC[C/G]ATCATCAGCCGAGTC | 57602 |
rs768330755 | snp | A/G | 3.60094e-05 | 0.00424304 | intron-variant | USP36 | GRCh38.p7 | 17:78829013 | CCCTGGTGGCCTGCC[A/G]GCGTGGAAGGAGGAG | 57602 |
rs768352524 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810426 | CTGAGTAGCTGGGAA[C/T]ACAGGCACGTGCCAT | 57602 |
rs768372537 | in-del | -/G | 4.24908e-05 | 0.00460908 | intron-variant | USP36 | GRCh38.p7 | 17:78821092 | GGCAGTGGAGCAGGT[-/G]GGGCCTGGCAGAGGC | 57602 |
rs768387211 | snp | A/G | 3.29848e-05 | 0.00406095 | intron-variant | USP36 | GRCh38.p7 | 17:78818787 | CTTGCATCTATGAAG[A/G]AGGTGATGAGAAAGA | 57602 |
rs768428933 | snp | A/G | 8.35108e-05 | 0.0064613 | intron-variant | USP36 | GRCh38.p7 | 17:78827196 | TTCTGCTGCCACCAT[A/G]TAGAAAAGGTGTCCA | 57602 |
rs768486520 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814478 | CAGGACAGCATAGAG[C/T]CCATACATGACAGGA | 57602 |
rs768522985 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78801852 | ATTCACAGAATGTTT[C/T]AAAGTTCATGTGCAC | 57602 |
rs768525057 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824865 | GCAAAAGCAGGGGCT[G/T]CAGCACTGACACTGG | 57602 |
rs768525189 | snp | C/T | 1.71631e-05 | 0.00292938 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803790 | CTCTGGGGGGGCTCA[C/T]TGGCCTCTGGCAACT | 57602 |
rs768574640 | snp | A/C | 6.60393e-05 | 0.00574589 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798532 | CTCTTCTCTCTCTTA[A/C]ATTTTTTAATTTTCT | 57602 |
rs768578264 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808560 | CCTGCCTGTCGGCCT[A/G]TCTTTGACATTTTAC | 57602 |
rs768580370 | snp | A/C | 1.73833e-05 | 0.00294811 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803866 | TCGAGATGGAGGAGC[A/C]GCTCCGTGGTTCTGA | 57602 |
rs768607857 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812936 | ATCACACTCGGGCGG[C/T]CGGGAAGGGAGGAGG | 57602 |
rs768657247 | in-del | -/CTGGGGACACCGCAACCCTCCTC | | | intron-variant | USP36 | GRCh38.p7 | 17:78825813 | CTCCCCCTGCAGGTG[-/CTGGGGACACCGCAACCCTCCTC]CTGGGGACACCTACT | 57602 |
rs768662830 | snp | A/C | 4.99048e-05 | 0.00499499 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807507 | GTTTGGGGGAAGGGG[A/C]CCCCGAGGGCAGCTT | 57602 |
rs768682756 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817157 | GACAGGAACAGGCTG[C/T]GTAGGTTTGTGGCCT | 57602 |
rs768686464 | snp | C/T | 3.30109e-05 | 0.00406256 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807129 | TCGTTTCCTGAGAAT[C/T]GCAGAGATGGGCCGC | 57602 |
rs768701772 | snp | G/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842498 | AGCTACTAGGGAGGC[G/T]GAGACAGGAGAATCG | 57602 |
rs768771491 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788668 | GAAGGCATGAAGGAA[A/G]GAAGGGCCAAGGACG | 57602 |
rs768793832 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78814805 | AATACAAAAAATTAG[C/T]TGGGCATGGTGGTGC | 57602 |
rs768804776 | snp | A/G | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787327 | TCAAAGTTTATCAAT[A/G]GCAAACAGGTTAACT | 57602 |
rs768835204 | snp | A/C | 1.65839e-05 | 0.00287953 | intron-variant | USP36 | GRCh38.p7 | 17:78813043 | AATTCTCTTACTAGG[A/C]ATTACAGAAACGGAG | 57602 |
rs768845003 | snp | G/T | 1.65932e-05 | 0.00288034 | intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806319 | AATAAAAACTTGGTG[G/T]TCTAAAAAAGGTTTC | 57602 |
rs768856388 | snp | A/C/T | 4.99524e-05 | 0.00499741 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835296 | GCTGCGAGCATGCTC[A/C/T]TTGGAGAGCAGGTAG | 57602 |
rs768866105 | snp | G/T | | | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803652 | TCCGGGCGCTTCTTC[G/T]TCTTCCTCTTCCTCT | 57602 |
rs768897457 | snp | A/G | 1.69309e-05 | 0.0029095 | intron-variant | USP36 | GRCh38.p7 | 17:78814575 | AAAAATCAAGGAAAA[A/G]ACAAATAAAATTCAC | 57602 |
rs768952333 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809181 | GGTTTTATTGCTTCA[C/T]TTGTTTGTAGTAAAT | 57602 |
rs768965584 | snp | A/G | 0.000168364 | 0.00917354 | intron-variant | USP36 | GRCh38.p7 | 17:78802315 | CCCACCCCCTCGCCC[A/G]GTGCATACCCATGCG | 57602 |
rs769008664 | snp | A/G | 4.23935e-05 | 0.0046038 | intron-variant | USP36 | GRCh38.p7 | 17:78821090 | GAGGCAGTGGAGCAG[A/G]TGGGGCCTGGCAGAG | 57602 |
rs769023609 | snp | A/G | 1.65833e-05 | 0.00287948 | splice-donor-variant | USP36 | GRCh38.p7 | 17:78806957 | GACCCCCACACACCC[A/G]CCTTCTTGGCAGAAA | 57602 |
rs769037727 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798645 | TCCTGCACACAGGCC[A/G]GGCTCTCATGAGCTC | 57602 |
rs769067138 | snp | A/G | 0.000150011 | 0.00865928 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807217 | GCTGGAGCTGCTGGA[A/G]CCCCTCCTGTCGAGG | 57602 |
rs769076586 | snp | A/G | 2.34074e-05 | 0.00342099 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821021 | GACGTCCAAGTAGGG[A/G]TCGTAGGTGTCCGAG | 57602 |
rs769127788 | snp | C/G | 2.9066e-05 | 0.0038121 | intron-variant | USP36 | GRCh38.p7 | 17:78820973 | ACTGCAAAAGTGAAG[C/G]GCAGGACAGATCTGT | 57602 |
rs769140395 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794290 | TCAGCCTCAGGAGTC[G/T]AAAAAGCACATCAGA | 57602 |
rs769146023 | snp | C/G | 1.64939e-05 | 0.0028717 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803538 | CCATCTTCCTGCCGT[C/G]TGACAGCGGGCAGCT | 57602 |
rs769152603 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798949 | AGTCATCAACCACGG[A/T]CTCAGTCCGGGCCTG | 57602 |
rs769156620 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838134 | ACGCCTGTAATCCCA[A/G]CACTTGGGAGGCCGA | 57602 |
rs769184341 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78829515 | ATACATCTGGGGTTG[A/C]AAATGTTTTCTGGGA | 57602 |
rs769202995 | snp | C/T | 1.65198e-05 | 0.00287395 | intron-variant | USP36 | GRCh38.p7 | 17:78798865 | TGAGCTGAGCCACGC[C/T]GCCCTGCTCCCTCAA | 57602 |
rs769241982 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78825674 | ACTCCTCACGAATTT[A/C]TTCCACCGTAGACTC | 57602 |
rs769296470 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78811812 | GGTGGAGGTTGCAGC[A/G]AGCCAAGGTTGCGCC | 57602 |
rs769357187 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838945 | TGTAATGCACACGAT[A/G]TGAACACCTTAACCT | 57602 |
rs769378558 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820473 | GTCCCTCAAGCCCCT[A/G]TAAAAAAAAAGCAAA | 57602 |
rs769422414 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836204 | TGCTCTTTAAGGCCT[C/T]CAGCTGGTAGGAGAA | 57602 |
rs769424532 | in-del | -/G/GG | 7.45275e-05 | 0.00610403 | intron-variant | USP36 | GRCh38.p7 | 17:78827226 | AAGCCCTGGGAGGGT[-/G/GG]GGGTGGGGAAGCACG | 57602 |
rs769455920 | snp | A/G | 3.30087e-05 | 0.00406242 | intron-variant | USP36 | GRCh38.p7 | 17:78820050 | GTAAAATACACAGCA[A/G]AGGAAAAAGGCTGAT | 57602 |
rs769464988 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78792249 | TTTTTAGGATGGGAG[A/G]TGCCTGAACATGTTC | 57602 |
rs769475840 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836315 | CATCATCAGCCGAGT[C/T]CTTGCGGCCGGGTTT | 57602 |
rs769482719 | in-del | -/AGG | | | intron-variant | USP36 | GRCh38.p7 | 17:78793154 | AACCCTGAGGTAAGA[-/AGG]AGAAGAGAACAGAGG | 57602 |
rs769492360 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78810518 | CTCCTGGGATCCACT[A/G]ATCTTCCCACATCGG | 57602 |
rs769516646 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795715 | GGCTCCCCAGGCCCC[C/T]GGAAAGGAGGTGCAG | 57602 |
rs769519436 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812898 | TAATCCCATTGCCGA[C/T]GTTCTTCTTGGAGTG | 57602 |
rs769536607 | snp | C/T | 8.23906e-05 | 0.00641783 | intron-variant | USP36 | GRCh38.p7 | 17:78818660 | GGATGGTGTCACGAG[C/T]GCTCACCTTGGTGAT | 57602 |
rs769647756 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78826634 | CAAGGAAGTCCTAAG[C/T]ATTTCCTGCCTGTTT | 57602 |
rs769674374 | snp | G/T | 0.00018606 | 0.00964342 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803922 | GACAGCAATGTGGGG[G/T]GGGGGCTGAAGGGGG | 57602 |
rs769681382 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841249 | GGCAGGGAGAAGGCT[A/G]GGCTCCCCCACCTGC | 57602 |
rs769772115 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78826854 | AGAGACCTCATTCCT[-/A]ACCACCCCAACCTCT | 57602 |
rs769800839 | snp | A/C/T | 3.96764e-05 | 0.00445387 | intron-variant | USP36 | GRCh38.p7 | 17:78827240 | GTGGGTGGGGAAGCA[A/C/T]GCACTTGGCACAGCC | 57602 |
rs769806882 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791296 | TGCACCACCATGCCC[A/G]GCTGATTTTGTATTT | 57602 |
rs769820188 | snp | A/G | 0.000280101 | 0.011831 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806995 | TTTTTTGGCTGGTGG[A/G]GGAGACATGGTGCTT | 57602 |
rs769855490 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805328 | CACTTAAGGCCCTCC[C/G]ACGTACACAAATCTT | 57602 |
rs769866973 | snp | A/C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807866 | GTACCACCACACCTG[A/C/G]CTAATTTCTGTATTT | 57602 |
rs769877335 | snp | A/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842353 | CTGTAATCCTAGCAC[A/T]TTGGGAGGCCGAGGC | 57602 |
rs769886685 | in-del | -/CAT | 3.72232e-05 | 0.00431395 | intron-variant | USP36 | GRCh38.p7 | 17:78798900 | GTGGTCAGCATCACA[-/CAT]CATACCTTCCCTCGG | 57602 |
rs769899526 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800584 | TGTCCCCTGCCCCCA[C/T]ACAGTGGCTTCCATG | 57602 |
rs769902666 | snp | A/G | 3.00901e-05 | 0.00387868 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835489 | CCACAGCTCTCATAC[A/G]TGTGCTCACTGCCTG | 57602 |
rs769913674 | snp | A/G | 6.65945e-05 | 0.00576999 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835409 | CCACGCGGAAGACCC[A/G]CTCCCACCTCAGAGA | 57602 |
rs769916559 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816238 | ATTCATAGCTCACTG[C/T]AACTTCAAACTCCTG | 57602 |
rs769923241 | snp | C/T | 1.71155e-05 | 0.00292531 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803663 | CTTCTTCTTCCTCTT[C/T]CTCTTCCCGTGGGGA | 57602 |
rs769973055 | snp | A/G | 1.78742e-05 | 0.00298945 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807590 | GATATGGGCACACCA[A/G]TCTCTTCAGTGGTGT | 57602 |
rs770010144 | in-del | -/GAGGCTGCATAGTGGCA | | | intron-variant | USP36 | GRCh38.p7 | 17:78811047 | TGAACCCAAGAGGCG[-/GAGGCTGCATAGTGGCA]GAGGCTGCAGTGAGC | 57602 |
rs770028770 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78809331 | AAGTTTTGTTTTGTT[-/C]CCCTACATTCTATTC | 57602 |
rs770033033 | snp | C/T | 3.29881e-05 | 0.00406115 | intron-variant | USP36 | GRCh38.p7 | 17:78821905 | ATGTTCTAATCCTGG[C/T]AAGAAGCAGTAGAAC | 57602 |
rs770090124 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823323 | AGCTGCGTGTGATGG[C/T]GGCTACCAAAATCCA | 57602 |
rs770101304 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808381 | TCAGCTGCCCAACTG[A/G]CTAGGACTATAGGAG | 57602 |
rs770127933 | snp | A/G | 2.74578e-05 | 0.00370515 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802388 | GGACTCGGGGACAAC[A/G]GCATCTTGGGGCTTG | 57602 |
rs770215038 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815851 | CATACACACACACAT[-/AT]GCATGCATACACATG | 57602 |
rs770224635 | snp | A/G | | | downstream-variant-500B | USP36 | GRCh38.p7 | 17:78787119 | TAGCTGGGATTACAC[A/G]CACGCGCTACCACGC | 57602 |
rs770226414 | snp | A/G | 3.44364e-05 | 0.00414934 | intron-variant | USP36 | GRCh38.p7 | 17:78813897 | GCCAAGGATGTTGCA[A/G]AAAACAAAACAATCA | 57602 |
rs770245551 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | USP36 | GRCh38.p7 | 17:78799048 | AGACACGGGGGTCAG[C/T]ACGAGTGCAGGTTCC | 57602 |
rs770259865 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814675 | AACAATTTGGGGGCC[A/G]GGCACAGTGGCTCAC | 57602 |
rs770261328 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827793 | ATGTGCCTGTAGTCC[C/T]AGCTACTTAGGTGGC | 57602 |
rs770270047 | snp | A/G | 1.6918e-05 | 0.00290839 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836410 | AGAGCCATAGATAAC[A/G]AAATCCCGGGACAAA | 57602 |
rs770301401 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813838 | GCTGGAATGGACCAA[A/G]GAATCATTCATCTGG | 57602 |
rs770333347 | snp | C/T | 3.34202e-05 | 0.00408766 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836400 | GAAGAAACATAGAGC[C/T]ATAGATAACGAAATC | 57602 |
rs770356293 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78809523 | AAATGCTCATGGTCA[C/G]TGAAGCGCCCCTGCA | 57602 |
rs770365620 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819382 | TTCGAGACCAGCCTG[A/G]CCAACAAGGTGAAAC | 57602 |
rs770367607 | snp | A/G | 1.66676e-05 | 0.00288679 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807202 | GGCCGAGTGCTCTGG[A/G]CTGGAGCTGCTGGAG | 57602 |
rs770413198 | snp | G/T | 1.80328e-05 | 0.00300268 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803925 | AGCAATGTGGGGTGG[G/T]GGCTGAAGGGGGGTT | 57602 |
rs770434560 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829922 | ATTTTTTGTATTTTA[A/G]TAGAGACAGAGTTTC | 57602 |
rs770444949 | snp | C/T | 6.59174e-05 | 0.00574059 | splice-acceptor-variant | USP36 | GRCh38.p7 | 17:78822006 | TTTGACGATCCAACC[C/T]GAAAAGGAGACCCCA | 57602 |
rs770456981 | snp | A/G | 0.000181247 | 0.00951792 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813786 | ACCGCAGATAGAACA[A/G]CACGTAGGCCTGCTG | 57602 |
rs770505545 | in-del | -/ACAA/ACACAA | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836800 | TATACACACACGGAC[-/ACAA/ACACAA]ACACACACACACACA | 57602 |
rs770549188 | snp | C/T | 1.88542e-05 | 0.0030703 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827245 | TGGGGAAGCACGCAC[C/T]TGGCACAGCCATTCA | 57602 |
rs770560061 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820419 | AGTGAGCTATGATTG[C/T]GCCACTGCACTCCTG | 57602 |
rs770596891 | snp | G/T | 1.65381e-05 | 0.00287555 | intron-variant | USP36 | GRCh38.p7 | 17:78813027 | AAGAAAACAAGTAGG[G/T]AATTCTCTTACTAGG | 57602 |
rs770606163 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant | USP36 | GRCh38.p7 | 17:78798882 | CCCTGCTCCCTCAAG[C/T]CTGTGGTCAGCATCA | 57602 |
rs770618059 | snp | C/T | 4.94907e-05 | 0.00497422 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836324 | CCGAGTCCTTGCGGC[C/T]GGGTTTCAGGGCCTC | 57602 |
rs770655332 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793278 | AAGAGTAGTGGGCAC[A/G]TATGCAATGAGAGAG | 57602 |
rs770687275 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836728 | TTCCAAAGGTCATCA[C/T]GTGGTCCAAATGTCT | 57602 |
rs770689552 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824840 | ACAGCAAGGGGCCGG[C/T]GGAAACCCTGCAAAA | 57602 |
rs770704168 | snp | A/G | 1.82384e-05 | 0.00301974 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807606 | TCTCTTCAGTGGTGT[A/G]CGGCTTCTTCATCGT | 57602 |
rs770718156 | snp | G/T | 8.42708e-05 | 0.00649063 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802413 | GGCTTGGCACTCCTT[G/T]GGCATTTGAGATGCC | 57602 |
rs770729352 | in-del | -/CCAGGTCAGAACTA | 1.64751e-05 | 0.00287007 | intron-variant | USP36 | GRCh38.p7 | 17:78799013 | CGACATCTTGCCATC[-/CCAGGTCAGAACTA]CCAGGCAGACACGGG | 57602 |
rs770730253 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798885 | TGCTCCCTCAAGCCT[A/G]TGGTCAGCATCACAC | 57602 |
rs770743504 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794226 | CACCTGCTGTTCTCT[C/G]CACTCCACCAGCCGC | 57602 |
rs770750731 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802346 | GTCCCCAGGACACCA[A/G]CCATTCGCGGATGGT | 57602 |
rs770780299 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834024 | GGCCAAGGCGGTTGG[A/G]TCACCTGAGGTCACG | 57602 |
rs770819423 | in-del | -/GGTGAGGTCGGAGGATGGTGAGGGGGGA | 1.64833e-05 | 0.00287078 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806214 | GGTTTTCATGGGGTG[-/GGTGAGGTCGGAGGATGGTGAGGGGGGA]GGTGAGGTCGGAGGA | 57602 |
rs770828514 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807003 | CTGGTGGAGGAGACA[C/T]GGTGCTTGCAGGCTC | 57602 |
rs770877928 | snp | C/G | 4.35692e-05 | 0.00466719 | intron-variant | USP36 | GRCh38.p7 | 17:78804027 | TTCTGAAAGACCCAG[C/G]AGAGCTGTTCCTTCT | 57602 |
rs770924504 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839462 | TGAAGACATCCAGTC[A/G]TATTAAAAACTCCCC | 57602 |
rs770982212 | snp | G/T | 3.29913e-05 | 0.00406135 | intron-variant | USP36 | GRCh38.p7 | 17:78822039 | CTTTAAGGGAAGGGC[G/T]CAGCAAGATGACACG | 57602 |
rs770986163 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804198 | CAGGTACAGTGGCTC[A/G]TGCCTATAATTCCAG | 57602 |
rs770997723 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791238 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAC | 57602 |
rs771001303 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78807692 | AAGTCTCAGCTGGGC[C/T]ACATCTTCTTAAGGC | 57602 |
rs771024669 | snp | A/C/G | 0.000181255 | 0.00951822 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807081 | AATCTGCTCCACTTG[A/C/G]CGGCGTTTTGGAGTG | 57602 |
rs771027463 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818684 | TGGTGATCTTCCCCC[C/T]GCTGAAGTTGGCAAA | 57602 |
rs771045314 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78810154 | ACAAGGTCTCACTCT[-/C]GTCACCTTGCCTGGA | 57602 |
rs771195274 | snp | C/T | 1.79835e-05 | 0.00299857 | intron-variant | USP36 | GRCh38.p7 | 17:78813918 | AAAACAATCAACAAG[C/T]ATCCCATTATCCTCA | 57602 |
rs771212962 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78836083 | CCCGGAGTGAGGGCC[C/T]CTCTGCCAGCACACT | 57602 |
rs771239512 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816882 | ATGGACATGCAGAAC[A/G]TCAACTAGAAAATTC | 57602 |
rs771266583 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78808208 | TCCCAGTTTTATCTT[-/A]AAGCTATTATCTCAA | 57602 |
rs771271368 | snp | A/G | 1.82433e-05 | 0.00302016 | intron-variant | USP36 | GRCh38.p7 | 17:78829016 | TGGTGGCCTGCCGGC[A/G]TGGAAGGAGGAGCAA | 57602 |
rs771277017 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798423 | ACAGGGGCACAGTCA[C/G]CGGCGATAGCTGAGG | 57602 |
rs771314937 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814440 | TAATAGTGCCCGGCA[C/T]GGCAGCTGTAGCCCG | 57602 |
rs771322113 | snp | A/G | 3.54667e-05 | 0.00421095 | intron-variant | USP36 | GRCh38.p7 | 17:78835274 | CTGCTGCAAACCCAC[A/G]CTCACAGCTGCGAGC | 57602 |
rs771322558 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819944 | CTTAGCACACATGTA[A/G]GCATTCTCTCCACTC | 57602 |
rs771370714 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793544 | GCCACCTCCGGGCAA[A/G]AGTGTGACTCCAGGG | 57602 |
rs771374958 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78816148 | AGGAACTCCGAAAAA[A/C]ATACGCATAATTTTT | 57602 |
rs771376984 | snp | C/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807446 | TTCTTCACCTTCTTT[C/T]CAGGGTCGTCTAGGA | 57602 |
rs771377432 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78810635 | ACCAACTTTGCAATT[A/G]TATCATGTATTTTAC | 57602 |
rs771430214 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78813687 | ATTCCCAATTACCTT[A/C]AAACAAAAAAAGGTT | 57602 |
rs771464941 | snp | C/T | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795192 | GGGTCAGCAGTGTGC[C/T]CTGCTCTCTGCCACC | 57602 |
rs771473997 | snp | A/G | 1.66452e-05 | 0.00288484 | intron-variant | USP36 | GRCh38.p7 | 17:78828889 | TTTTAACATGGATTG[A/G]TGCTTACTTTTCAGG | 57602 |
rs771476212 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793153 | GAACCCTGAGGTAAG[A/G]AGGAGAAGAGAACAG | 57602 |
rs771484197 | snp | C/T | 1.89127e-05 | 0.00307506 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802431 | CATTTGAGATGCCCA[C/T]CCTCTTCTACTGCCC | 57602 |
rs771498657 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818453 | CTATTTTTAAAAGGC[A/G]TCCCAGGTTGCTTCC | 57602 |
rs771500160 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78827701 | TGAGCCCAGGAGTTC[A/G]AGGGCAGCCTGGGTA | 57602 |
rs771518797 | snp | C/G | 1.64776e-05 | 0.00287028 | intron-variant | USP36 | GRCh38.p7 | 17:78806110 | AAGCACACGCAACCA[C/G]AGGGAGAACCAGTTG | 57602 |
rs771522631 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78808607 | TACTGATACACATTA[A/G]CTGTATGGTTAATTT | 57602 |
rs771538294 | snp | A/G | 3.30164e-05 | 0.00406289 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807373 | GCTGCTATTCGAGTT[A/G]CTGGTCCCAGGCAGC | 57602 |
rs771571903 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806171 | CTGGCTCTATGGACG[C/G]GCCAAGTGGAGGCAA | 57602 |
rs771592302 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836130 | TCTCCTGGCCGGTGG[C/G]TCATCTCCACTCTTG | 57602 |
rs771668508 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805076 | GTGAGGCTCCCTCTT[C/G]CCAGCTATGTGTCTC | 57602 |
rs771680038 | snp | C/T | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807254 | CTCTCGTCGTTCCCC[C/T]TCAGCCCATGCCCGT | 57602 |
rs771694545 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828517 | AAGCTACCTGTCCTG[A/G]CCTGCCCCCACTAAG | 57602 |
rs771707735 | snp | A/G | 1.67371e-05 | 0.0028928 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836405 | AACATAGAGCCATAG[A/G]TAACGAAATCCCGGG | 57602 |
rs771709549 | snp | C/T | 3.29973e-05 | 0.00406172 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803555 | GACAGCGGGCAGCTG[C/T]GCCTGGCCCTCCCTC | 57602 |
rs771762893 | snp | A/C/G | 4.02077e-05 | 0.00448358 | intron-variant | USP36 | GRCh38.p7 | 17:78827352 | TCGGGCGATCTCTAA[A/C/G]AGAGGAAGAAACAGG | 57602 |
rs771774516 | in-del | -/TGAT | 1.65451e-05 | 0.00287615 | intron-variant | USP36 | GRCh38.p7 | 17:78818811 | AGAAAGATTAATGAA[-/TGAT]TGATTCGTGCTCTGA | 57602 |
rs771827935 | snp | A/G | 1.65026e-05 | 0.00287246 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807124 | ACAGTTCGTTTCCTG[A/G]GAATCGCAGAGATGG | 57602 |
rs771828330 | snp | A/G | | | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806216 | GTTTTCATGGGGTGG[A/G]TGAGGTCGGAGGATG | 57602 |
rs771843113 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant | USP36 | GRCh38.p7 | 17:78799038 | ACTACCAGGCAGACA[C/T]GGGGGTCAGCACGAG | 57602 |
rs771851998 | snp | A/C | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836102 | TGCCAGCACACTGCA[A/C]ATCTGTACCCTGTCT | 57602 |
rs771868545 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78808790 | ACCAAGAGGCTGTAC[A/C]CGTTATCTCTCTCGT | 57602 |
rs771893500 | in-del | -/GTG | 1.64743e-05 | 0.00287 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807019 | GTGCTTGCAGGCTCA[-/GTG]GTGGTGGTGTTGCTC | 57602 |
rs771906903 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836182 | TTGGGGTTGAGCAAC[A/G]CATATTTGCTCTTTA | 57602 |
rs771938638 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819267 | TTCTTTAGTGCCTAC[A/G]GCTTTACAAGGACCT | 57602 |
rs771984681 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788669 | AAGGCATGAAGGAAG[G/T]AAGGGCCAAGGACGA | 57602 |
rs772054491 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78804653 | AAAAAAAAAAAAAAA[A/G]GCAAGCCAACACGTG | 57602 |
rs772083577 | snp | A/G | 4.94271e-05 | 0.00497102 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798425 | AGGGGCACAGTCAGC[A/G]GCGATAGCTGAGGCT | 57602 |
rs772096874 | snp | A/G | 3.3012e-05 | 0.00406262 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799691 | CGTAAGCTTTATCAG[A/G]TGAGTATTTGAGCAG | 57602 |
rs772100222 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809267 | CAACTTTAAGCATAC[A/T]AAGTCTTCTTCCCTT | 57602 |
rs772120390 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814460 | GCTGTAGCCCGAGTG[C/T]ACCAGGACAGCATAG | 57602 |
rs772158740 | snp | A/C/G | 6.86183e-05 | 0.00585707 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803785 | AGGGGCTCTGGGGGG[A/C/G]CTCACTGGCCTCTGG | 57602 |
rs772159882 | snp | A/G | 3.30186e-05 | 0.00406303 | intron-variant | USP36 | GRCh38.p7 | 17:78819889 | GGGGACTTATTTCCC[A/G]TCTGGTATCAGTCTT | 57602 |
rs772163987 | snp | C/G | 1.66674e-05 | 0.00288676 | intron-variant | USP36 | GRCh38.p7 | 17:78812809 | AGTGTGAGGAGGTCT[C/G]TGAGGAGCACCAAGA | 57602 |
rs772201838 | snp | C/G/T | 3.33151e-05 | 0.00408126 | intron-variant | USP36 | GRCh38.p7 | 17:78814374 | ATGGGTGCTGAAACC[C/G/T]GTCCCAGGAGGCAGC | 57602 |
rs772258858 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78820584 | CTTGGGTTGGCCCAG[A/C]AAAGGCAGACCACCC | 57602 |
rs772340278 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78815793 | GCACACATATATACA[C/T]ACATGCATACATACA | 57602 |
rs772364490 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78799600 | CACCAGGATCCATTC[A/C]ACACCCTTCCCTCCT | 57602 |
rs772389787 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839147 | CAAAATTTTGCTTTG[C/T]TAAGTGTGGATTTTC | 57602 |
rs772426162 | snp | C/T | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807494 | GGTGTCTGGGAGAGT[C/T]TGGGGGAAGGGGACC | 57602 |
rs772461537 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789800 | CTCTAGTTCCTGCTA[C/G]ACTTCACCAAAATGT | 57602 |
rs772497092 | snp | A/G | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795882 | AATTCAACAGACCCA[A/G]ATCCTAAGTCAACCA | 57602 |
rs772526701 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78795144 | TACAACGCAAATGCC[-/T]TCAGACACAGCCTGG | 57602 |
rs772632998 | in-del | -/A | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796040 | GAAGGGACGTGACTC[-/A]CACCCAACAGTGATA | 57602 |
rs772675333 | snp | A/G | 4.94768e-05 | 0.00497352 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806241 | AGGATGGTGAGGGGG[A/G]AGGTGGACGGAGGTC | 57602 |
rs772710931 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793169 | AGGAGAAGAGAACAG[A/G]GGGAGAGGAGCTGGT | 57602 |
rs772725826 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792556 | ATGCACATTCTCAGG[C/T]CTCATCCCAGACCTG | 57602 |
rs772732991 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818482 | CCCCTCTCTGTGACT[C/G]TCTTCCCGTCCTGGA | 57602 |
rs772754000 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841473 | GATTTGACCTTTGTA[A/G]GCTGGTGGCGGCTGT | 57602 |
rs772762884 | snp | A/C | 1.65537e-05 | 0.0028769 | intron-variant | USP36 | GRCh38.p7 | 17:78798559 | TTCTTTTCCTAGACC[A/C]AGAATCACAGGCATC | 57602 |
rs772769833 | snp | A/G/T | 3.31177e-05 | 0.00406914 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807161 | CCACTCCTGGGGGTC[A/G/T]GGGGGGCCTTGGTGG | 57602 |
rs772772101 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825678 | CTCACGAATTTCTTC[C/T]ACCGTAGACTCTGGT | 57602 |
rs772785572 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823800 | CTATCCTAGACTATC[A/G]ACCCTTCTGCTGCCA | 57602 |
rs772805476 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812903 | CCATTGCCGATGTTC[C/T]TCTTGGAGTGATCTG | 57602 |
rs772809219 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant | USP36 | GRCh38.p7 | 17:78820055 | ATACACAGCAGAGGA[A/G]AAAGGCTGATTCAAG | 57602 |
rs772820975 | snp | A/G | 5.23446e-05 | 0.00511562 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803880 | CAGCTCCGTGGTTCT[A/G]ACGTCCCTGGGGGCT | 57602 |
rs772858458 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812945 | GGGCGGCCGGGAAGG[A/G]AGGAGGAGCCTGTCC | 57602 |
rs772869063 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832796 | TGAAAGTCCACCCAG[A/G]ACCACCTCAAAATTA | 57602 |
rs772869882 | snp | G/T | 1.6492e-05 | 0.00287154 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836318 | CATCAGCCGAGTCCT[G/T]GCGGCCGGGTTTCAG | 57602 |
rs773037826 | snp | C/G | 4.94279e-05 | 0.00497107 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836215 | GCCTCCAGCTGGTAG[C/G]AGAAGCTCTTGCTGG | 57602 |
rs773048293 | snp | A/C/G | 0.000144261 | 0.00849196 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803924 | CAGCAATGTGGGGTG[A/C/G]GGGCTGAAGGGGGGT | 57602 |
rs773069319 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810234 | TTCAAGTGATCCTCC[C/T]CCAACAGCTTACTGA | 57602 |
rs773076856 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798852 | ACTGCCCCGGCTCTG[A/G]GCTGAGCCACGCCGC | 57602 |
rs773091459 | in-del | -/CAAC | 1.64732e-05 | 0.0028699 | frameshift-variant, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798940 | CTTCGTCCCAGTCAT[-/CAAC]CACGGTCTCAGTCCG | 57602 |
rs773091571 | snp | C/T | 1.65677e-05 | 0.00287812 | intron-variant | USP36 | GRCh38.p7 | 17:78818617 | TTCGTGTTATTCTGA[C/T]GCCGACTGTGGCCCA | 57602 |
rs773140919 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805473 | AGAACTAGAACCCAG[C/T]GCCGAGGCCACCAGT | 57602 |
rs773164578 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78788761 | CAGGACATCATCTAC[A/G]GCCTCCCCTCCACCA | 57602 |
rs773278219 | snp | C/T | 1.72323e-05 | 0.00293528 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803671 | TCCTCTTCCTCTTCC[C/T]GTGGGGAGCCGCAGT | 57602 |
rs773305844 | snp | C/T | 7.63373e-05 | 0.00617761 | intron-variant | USP36 | GRCh38.p7 | 17:78802275 | CGGTCCCCCAACCCC[C/T]CGCCCGGTGCACACC | 57602 |
rs773321576 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838264 | TGTAATCCCAGCTAC[A/G]CAGGAGGCTGAGGCA | 57602 |
rs773335098 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78839211 | ATAAAATTAAGGTTC[C/G]TAAAAACAGTTTACA | 57602 |
rs773371986 | snp | G/T | 3.06819e-05 | 0.00391663 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835490 | CACAGCTCTCATACG[G/T]GTGCTCACTGCCTGA | 57602 |
rs773387266 | snp | C/T | 3.39853e-05 | 0.00412207 | intron-variant | USP36 | GRCh38.p7 | 17:78806928 | GGAGCTCTCCTGATA[C/T]ACAGCAGCGGCGAGA | 57602 |
rs773395961 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | USP36 | GRCh38.p7 | 17:78813735 | TAAGAAAAGAGCAGA[A/G]GGAGTGAGCTCATCT | 57602 |
rs773403969 | snp | C/T | 1.64827e-05 | 0.00287073 | intron-variant | USP36 | GRCh38.p7 | 17:78821915 | CCTGGCAAGAAGCAG[C/T]AGAACAAACGTCTCC | 57602 |
rs773436494 | snp | A/G | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806998 | TTTGGCTGGTGGAGG[A/G]GACATGGTGCTTGCA | 57602 |
rs773437185 | snp | C/T | 3.30196e-05 | 0.00406309 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807367 | AGATCTGCTGCTATT[C/T]GAGTTGCTGGTCCCA | 57602 |
rs773490397 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806188 | CCAAGTGGAGGCAAC[A/G]ACGGGGTGAGAGGTT | 57602 |
rs773490690 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812228 | TAAAGGAAATAAAAG[A/G]AGTGCACACAGAAAG | 57602 |
rs773530065 | in-del | -/TTTC | | | intron-variant | USP36 | GRCh38.p7 | 17:78790283 | TTAGTGGAGATATGG[-/TTTC]TTTTTCTTTTTCTTT | 57602 |
rs773543413 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78789875 | GGAAGGCAATGTGAA[A/G]GGGAATTAGTGCAGT | 57602 |
rs773578908 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78810906 | ATCACTTGAGGTCAG[C/G]AGTTCCAGACCAGCC | 57602 |
rs773610087 | snp | A/G/T | 7.60115e-05 | 0.00616448 | synonymous-codon, missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802447 | CCTCTTCTACTGCCC[A/G/T]CTGTGTCTCCTGCTT | 57602 |
rs773611755 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790813 | TGAAATCTGGTCTCA[C/T]GATGGTAAGAAGCTA | 57602 |
rs773615965 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | USP36 | GRCh38.p7 | 17:78806138 | TTGGCACCCAGAAGA[C/T]CCCGGCCCAAAGCTT | 57602 |
rs773635221 | snp | C/G/T | 0.000123753 | 0.00786538 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821033 | GGGGTCGTAGGTGTC[C/G/T]GAGACGCTCTTGCAC | 57602 |
rs773644722 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78834166 | ACAGGAGAATTGCTT[C/G]CACCCAGGAGGCGGA | 57602 |
rs773680276 | in-del | -/AAAAG | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842288 | GCGAGACTCCGTCTC[-/AAAAG]AAAAGAAAAGAAAAG | 57602 |
rs773770478 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | USP36 | GRCh38.p7 | 17:78806107 | GCCAAGCACACGCAA[C/T]CACAGGGAGAACCAG | 57602 |
rs773774964 | snp | A/C | 1.6666e-05 | 0.00288664 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807265 | CCCCTTCAGCCCATG[A/C]CCGTTGGCAGTGGCT | 57602 |
rs773808717 | snp | C/T | 6.59098e-05 | 0.00574026 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813789 | GCAGATAGAACAGCA[C/T]GTAGGCCTGCTGGTT | 57602 |
rs773813684 | snp | C/G | 1.65116e-05 | 0.00287324 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836336 | GGCCGGGTTTCAGGG[C/G]CTCCTTCAACTTATC | 57602 |
rs773848703 | snp | C/T | | | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803472 | CTGCTGCTCGCGTGG[C/T]GGCCGTCCGTAACAC | 57602 |
rs773873742 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792318 | TAATGGAGCAAGGTC[C/T]CCAGGGTGGAAGAAG | 57602 |
rs773899585 | snp | C/G | 1.80422e-05 | 0.00300346 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803926 | GCAATGTGGGGTGGG[C/G]GCTGAAGGGGGGTTG | 57602 |
rs773941307 | snp | C/T | 3.30825e-05 | 0.00406696 | intron-variant | USP36 | GRCh38.p7 | 17:78813031 | AAACAAGTAGGGAAT[C/T]CTCTTACTAGGCATT | 57602 |
rs773943075 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78825776 | TGCCCAGAGCCAGGC[C/G]CCCTGCTATAGGCTC | 57602 |
rs773950948 | snp | A/C | 1.65002e-05 | 0.00287225 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802349 | CCCAGGACACCAGCC[A/C]TTCGCGGATGGTGCG | 57602 |
rs773993759 | snp | C/T | 3.33267e-05 | 0.00408194 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807204 | CCGAGTGCTCTGGGC[C/T]GGAGCTGCTGGAGCC | 57602 |
rs773999350 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842672 | TTCAGCCATCTTCTA[C/T]AGGCTGTGAAACCAG | 57602 |
rs774069353 | in-del | -/CCCGGTGCACACCCATGCGGTCCCCCAACCCCTCA | 0.000118701 | 0.00770303 | intron-variant | USP36 | GRCh38.p7 | 17:78802277 | TCCCCCAACCCCTCG[lengthTooLong]CCCGGTGCACACCCA | 57602 |
rs774110042 | in-del | -/TTTG | | | intron-variant | USP36 | GRCh38.p7 | 17:78809629 | GCAAGTGGGGCTTCC[-/TTTG]TTTTTCTGGGGTTTT | 57602 |
rs774157603 | in-del | -/C | 1.675e-05 | 0.00289391 | intron-variant | USP36 | GRCh38.p7 | 17:78806943 | ACAGCAGCGGCGAGA[-/C]CCCCCACACACCCAC | 57602 |
rs774163158 | snp | A/C/T | 5.48605e-05 | 0.00523715 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807607 | CTCTTCAGTGGTGTG[A/C/T]GGCTTCTTCATCGTC | 57602 |
rs774168862 | snp | C/T | 2.09861e-05 | 0.00323923 | intron-variant | USP36 | GRCh38.p7 | 17:78807681 | GAGGAAGCGAGAAGT[C/T]TCAGCTGGGCCACAT | 57602 |
rs774233829 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797276 | CTCTGCTCTCCAGGA[C/T]AGTTGAGAGCTACTC | 57602 |
rs774277225 | snp | C/T | 5.57025e-05 | 0.00527714 | intron-variant | USP36 | GRCh38.p7 | 17:78813923 | AATCAACAAGCATCC[C/T]ATTATCCTCACTTTT | 57602 |
rs774289838 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831566 | TGCAGTGAGCCGAGA[C/T]TGTGGCAACTGCACT | 57602 |
rs774304737 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832163 | AGGACAGGACTGAAC[C/T]GCGTTCCTCCTAGAC | 57602 |
rs774322144 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78797944 | CTTCCCACTGCCACC[C/G]TCGGGTATGAGTCCA | 57602 |
rs774336659 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805477 | CTAGAACCCAGCGCC[A/G]AGGCCACCAGTACAG | 57602 |
rs774365708 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78814876 | GAATCACTTGAACCC[A/G]CGAGGCAGAGGTTGC | 57602 |
rs774387121 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818685 | GGTGATCTTCCCCCC[A/G]CTGAAGTTGGCAAAG | 57602 |
rs774428151 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78807938 | CAAACTTCTGGCCTC[A/G]AGCAGTCCACCTGCC | 57602 |
rs774455798 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815670 | ATCAGAAGAAAGGTC[A/G]TGCTAAAATGTCTTC | 57602 |
rs774461381 | snp | A/C | 1.65034e-05 | 0.00287253 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799682 | CTTTTCTCCCGTAAG[A/C]TTTATCAGATGAGTA | 57602 |
rs774490966 | snp | A/C | 1.65023e-05 | 0.00287244 | intron-variant | USP36 | GRCh38.p7 | 17:78822044 | AGGGAAGGGCTCAGC[A/C]AGATGACACGAGGGA | 57602 |
rs774516360 | snp | A/G | 1.72012e-05 | 0.00293263 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803677 | TCCTCTTCCCGTGGG[A/G]AGCCGCAGTGGCCTC | 57602 |
rs774602290 | in-del | -/CACACA | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836797 | GGTTATACACACACG[-/CACACA]GACACACACACACAC | 57602 |
rs774617830 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803456 | TTTCCTCCTCCGCTT[C/T]CTGCTGCTCGCGTGG | 57602 |
rs774648264 | in-del | -/AG | | | intron-variant | USP36 | GRCh38.p7 | 17:78788908 | TGCTGGCTTCACGAA[-/AG]AGAGATGAGGCCAGG | 57602 |
rs774662842 | snp | C/T | 4.94939e-05 | 0.00497439 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828925 | GATGAAGGAGACGGG[C/T]TTGATGGCGTTGCCG | 57602 |
rs774672935 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78820493 | AAAAAAGCAAAGCAA[A/C]GAAATGACAGCTGCA | 57602 |
rs774673908 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78819951 | CACATGTAGGCATTC[C/T]CTCCACTCAGGACAT | 57602 |
rs774682738 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830153 | ACCTTCATTCAAAGT[C/T]ACCACTATCCTGAAT | 57602 |
rs774713424 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794396 | GCTGAGTCCTGCTGG[C/T]CAGCTCCCACTGCCA | 57602 |
rs774736919 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836663 | CCATGTGCATCTCTT[C/T]ATCAGATACTCATCA | 57602 |
rs774745390 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809689 | CAGGCTGGAGCGCAG[C/T]GGCACAATGATAGCT | 57602 |
rs774847031 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78838947 | TAATGCACACGATAT[A/G]AACACCTTAACCTTG | 57602 |
rs774921364 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800301 | CAGGGGTGGAGGGAA[C/T]GGCCAAGCTTGGCTG | 57602 |
rs774964584 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78819616 | CGTCCTCTTGGTGTG[C/G]CCCCATGGCTGGTCA | 57602 |
rs774965047 | snp | A/G | 0.000116576 | 0.00763378 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807258 | CGTCGTTCCCCTTCA[A/G]CCCATGCCCGTTGGC | 57602 |
rs774988287 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793594 | ACACAGAAAGCTGCC[C/T]GTCTGCATGTCACGT | 57602 |
rs774989118 | snp | A/C/G | 5.51347e-05 | 0.00525022 | intron-variant | USP36 | GRCh38.p7 | 17:78829018 | GTGGCCTGCCGGCGT[A/C/G]GAAGGAGGAGCAATT | 57602 |
rs775000525 | snp | A/G | 3.30366e-05 | 0.00406413 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807449 | TTCACCTTCTTTCCA[A/G]GGTCGTCTAGGATGG | 57602 |
rs775007709 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78811846 | GCACTCCAGCCTGGG[C/T]GACAGAATGAGACTC | 57602 |
rs775014668 | snp | A/G | 9.88712e-05 | 0.00703035 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806194 | GGAGGCAACGACGGG[A/G]TGAGAGGTTTTCATG | 57602 |
rs775015140 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78802575 | TCAGCTCTGAGCAAA[C/T]TGGAAGGGGAGCAGG | 57602 |
rs775033013 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78793561 | GTGTGACTCCAGGGA[A/G]TCAGCTCAGCTGACA | 57602 |
rs775033972 | snp | C/G | 1.64787e-05 | 0.00287038 | intron-variant | USP36 | GRCh38.p7 | 17:78802542 | GGAGAGCAGCTGCTT[C/G]GAAGTGAGAGGCAGC | 57602 |
rs775044652 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818776 | GGAACCTTCTTCTTG[C/T]ATCTATGAAGAAGGT | 57602 |
rs775059509 | in-del | -/G | 1.64882e-05 | 0.00287121 | frameshift-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807102 | TTTGGAGTGGCCAGC[-/G]GGTGGAACAGTTCGT | 57602 |
rs775093635 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78790353 | TGGAGCACAATGGCG[C/T]GGTCTCAGCTCACTG | 57602 |
rs775098038 | snp | A/C/T | 3.30231e-05 | 0.00406333 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807137 | TGAGAATCGCAGAGA[A/C/T]GGGCCGCTCCACTCC | 57602 |
rs775104906 | snp | A/G | 3.6667e-05 | 0.00428161 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807609 | CTTCAGTGGTGTGCG[A/G]CTTCTTCATCGTCCC | 57602 |
rs775118247 | snp | A/C | 1.64898e-05 | 0.00287135 | intron-variant | USP36 | GRCh38.p7 | 17:78798379 | CCACCTCACCCTTAC[A/C]CCCACCCCCTCGGAA | 57602 |
rs775119483 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810546 | CGGCTTCCCAAAGTG[C/T]TGGAATTACAGACAT | 57602 |
rs775130762 | snp | C/T | 3.42255e-05 | 0.00413661 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803755 | CTCCCACAAAGGTCT[C/T]TTTCCTCTTCTCAGA | 57602 |
rs775133928 | snp | A/C/T | 1.6477e-05 | 0.00287024 | intron-variant | USP36 | GRCh38.p7 | 17:78806120 | AACCACAGGGAGAAC[A/C/T]AGTTGGCACCCAGAA | 57602 |
rs775137021 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798943 | CGTCCCAGTCATCAA[C/T]CACGGTCTCAGTCCG | 57602 |
rs775242963 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834147 | AGCTATTTGGGAGGC[C/T]GAGACAGGAGAATTG | 57602 |
rs775270487 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791315 | GATTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC | 57602 |
rs775280247 | snp | C/T | 3.30808e-05 | 0.00406686 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828900 | ATTGATGCTTACTTT[C/T]CAGGTCTCGGATGAA | 57602 |
rs775340832 | snp | C/T | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842466 | AGCTGGGTATGGTGG[C/T]GCACGCCTGTAATCC | 57602 |
rs775346803 | snp | A/G | 7.87557e-05 | 0.00627468 | intron-variant | USP36 | GRCh38.p7 | 17:78835543 | AAAGAGGAAGACGTA[A/G]GTCCACACACAGGTC | 57602 |
rs775352553 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78818702 | TGAAGTTGGCAAAGC[A/G]CTTGAGGGAAAGGGT | 57602 |
rs775370330 | snp | A/G | 1.66771e-05 | 0.00288761 | intron-variant | USP36 | GRCh38.p7 | 17:78799787 | CAATCGGAGCAGCCA[A/G]GAAACATTTACAGAC | 57602 |
rs775375082 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816977 | TGCCTGTTCTTAAAC[A/G]TCACATACCATCAGT | 57602 |
rs775407082 | snp | A/G/T | 6.6091e-05 | 0.00574819 | missense, synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807454 | CTTCTTTCCAGGGTC[A/G/T]TCTAGGATGGTTGGC | 57602 |
rs775411653 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807125 | CAGTTCGTTTCCTGA[A/G]AATCGCAGAGATGGG | 57602 |
rs775430572 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841273 | CACCTGCCCCTGGCC[A/G]TCAGGTGGCTGTGGA | 57602 |
rs775449344 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836111 | ACTGCACATCTGTAC[A/C]CTGTCTCCTGGCCGG | 57602 |
rs775478730 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78813896 | AGCCAAGGATGTTGC[A/G]GAAAACAAAACAATC | 57602 |
rs775518157 | snp | A/G | 1.66749e-05 | 0.00288741 | intron-variant | USP36 | GRCh38.p7 | 17:78812811 | TGTGAGGAGGTCTGT[A/G]AGGAGCACCAAGACC | 57602 |
rs775520129 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837543 | TCCCTAACAGAGGAT[C/T]GATACTGTTGGTGCA | 57602 |
rs775539051 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832024 | AATCTAAGCCAGGTT[C/G]TCCAGCAATATATGA | 57602 |
rs775553332 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78794024 | ACTTGGCCTCCGAAC[C/G]CAACTAACCACCCTA | 57602 |
rs775573263 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812882 | GTCAGTGGGGAGGAA[A/G]TAATCCCATTGCCGA | 57602 |
rs775617689 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78822686 | GCCTCCCACGCCTAC[A/G]TATCCATATGGTAGC | 57602 |
rs775626789 | snp | C/G/T | 0.000169535 | 0.00920536 | intron-variant | USP36 | GRCh38.p7 | 17:78827195 | GTTCTGCTGCCACCA[C/G/T]GTAGAAAAGGTGTCC | 57602 |
rs775733811 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823324 | GCTGCGTGTGATGGC[A/G]GCTACCAAAATCCAG | 57602 |
rs775764576 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797157 | AAGACCTGCGGGTTA[C/T]TGCAGCTGCAAGGGA | 57602 |
rs775770890 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | USP36 | GRCh38.p7 | 17:78798886 | GCTCCCTCAAGCCTG[C/T]GGTCAGCATCACACA | 57602 |
rs775796866 | snp | C/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812947 | GCGGCCGGGAAGGGA[C/G]GAGGAGCCTGTCCTG | 57602 |
rs775799449 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799692 | GTAAGCTTTATCAGA[C/T]GAGTATTTGAGCAGT | 57602 |
rs775825158 | in-del | -/ACACAA/ACAT | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836806 | CACACGGACACACAC[-/ACACAA/ACAT]ACACACACACACAAA | 57602 |
rs775844255 | snp | A/C | 4.95176e-05 | 0.00497558 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807385 | GTTGCTGGTCCCAGG[A/C]AGCCCCTGAGCAGTT | 57602 |
rs775873476 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78814700 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 57602 |
rs775893858 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78838056 | CGCCTGTGAATAGCC[A/G]GTGCAGTCCAGCCTG | 57602 |
rs775903450 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836412 | AGCCATAGATAACGA[A/T]ATCCCGGGACAAAAA | 57602 |
rs775921576 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818572 | GGTACTGTGTAAACA[A/G]CAGCTATCAAACTCG | 57602 |
rs775921818 | snp | A/G | 4.97121e-05 | 0.00498534 | intron-variant | USP36 | GRCh38.p7 | 17:78798569 | AGACCAAGAATCACA[A/G]GCATCACAGTTCCCA | 57602 |
rs776024932 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793422 | AGACAGCCCTGAAAG[C/T]CGAATCCATGGCACC | 57602 |
rs776050277 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798437 | AGCGGCGATAGCTGA[A/G]GCTGGCAGCCTTTGC | 57602 |
rs776054280 | snp | A/G | 3.30409e-05 | 0.0040644 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803436 | TCACCAAGACCTTCT[A/G]CTCCTTTCCTCCTCC | 57602 |
rs776081674 | snp | G/T | 1.6498e-05 | 0.00287206 | intron-variant | USP36 | GRCh38.p7 | 17:78818790 | GCATCTATGAAGAAG[G/T]TGATGAGAAAGATTA | 57602 |
rs776087734 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810579 | GTCACAGTCCCAGGC[C/T]CAGGCTGCTTCCTAA | 57602 |
rs776089283 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797462 | GTGGCGTCAGCCCCG[A/G]GAAGCAAGGGATGGC | 57602 |
rs776099574 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78827800 | TGTAGTCCCAGCTAC[C/T]TAGGTGGCTGAGGCA | 57602 |
rs776100532 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806247 | GTGAGGGGGGAGGTG[A/G]ACGGAGGTCATTGCC | 57602 |
rs776136296 | snp | A/C | 1.65266e-05 | 0.00287455 | intron-variant | USP36 | GRCh38.p7 | 17:78820061 | AGCAGAGGAAAAAGG[A/C]TGATTCAAGAAATGC | 57602 |
rs776156244 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810201 | ATGGCTCACTGCATA[C/T]AGCCTCAACCTCCCG | 57602 |
rs776197035 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78838018 | TGAGGGCAGGAGCCT[C/G]AGGCTGCAGTGAGCT | 57602 |
rs776216596 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815958 | CATGCATGCACACAC[-/AT]ATACATACACACACA | 57602 |
rs776236548 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836126 | CCTGTCTCCTGGCCG[A/G]TGGGTCATCTCCACT | 57602 |
rs776240175 | in-del | -/GCTCCCAGATCTGCT | 1.65124e-05 | 0.00287331 | cds-indel, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807346 | GGAGCCCTGCCTTTG[-/GCTCCCAGATCTGCT]GCTATTCGAGTTGCT | 57602 |
rs776288879 | snp | C/G | 4.95462e-05 | 0.00497701 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78799709 | AGTATTTGAGCAGTT[C/G]CTGGACCACATCAGA | 57602 |
rs776290049 | snp | A/T | 2.73452e-05 | 0.00369755 | intron-variant | USP36 | GRCh38.p7 | 17:78802569 | CAGCAGTCAGCTCTG[A/T]GCAAATTGGAAGGGG | 57602 |
rs776362086 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833571 | ATTCTTCCATAGACC[A/T]GGGACATTCTCAAAA | 57602 |
rs776398399 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794239 | CTGCACTCCACCAGC[C/T]GCCTTTCAGGCCATC | 57602 |
rs776400567 | in-del | -/G | 2.62968e-05 | 0.00362597 | intron-variant | USP36 | GRCh38.p7 | 17:78827118 | CCAGAGGCAAATTCT[-/G]CCACGTCTACCCAAG | 57602 |
rs776466430 | snp | G/T | 0.000135615 | 0.0082334 | intron-variant | USP36 | GRCh38.p7 | 17:78827232 | CTGGGAGGGTGGGTG[G/T]GGAAGCACGCACTTG | 57602 |
rs776499296 | snp | C/T | 6.25332e-05 | 0.00559131 | intron-variant | USP36 | GRCh38.p7 | 17:78827208 | CATGTAGAAAAGGTG[C/T]CCAAAGCCCTGGGAG | 57602 |
rs776534988 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816053 | CCTGGCATGGCAGCT[A/G]TAGGCTGAGTGCACC | 57602 |
rs776541145 | snp | A/G | 1.67894e-05 | 0.00289731 | intron-variant | USP36 | GRCh38.p7 | 17:78799810 | TTACAGACGTTTAAA[A/G]TAACCCACTGGGGAA | 57602 |
rs776575805 | snp | C/T | 0.000262985 | 0.011464 | intron-variant | USP36 | GRCh38.p7 | 17:78827049 | GTCTCCGGAGACAGC[C/T]CTTTCCCAGGAAGCA | 57602 |
rs776618341 | snp | A/G | 1.65002e-05 | 0.00287225 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803561 | GGGCAGCTGTGCCTG[A/G]CCCTCCCTCCTGTAC | 57602 |
rs776632323 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78796110 | GAGTTAACGAATGTA[C/T]GTACCCCAGGAAAAG | 57602 |
rs776672459 | snp | A/G | 8.25375e-05 | 0.00642355 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807130 | CGTTTCCTGAGAATC[A/G]CAGAGATGGGCCGCT | 57602 |
rs776677280 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78840896 | CTGCGCTAACTCCGA[A/T]AGGGTTGGGAGGCTT | 57602 |
rs776722272 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78796961 | AAAAGTAATCTTCTT[A/G]AGTTATACAATCATT | 57602 |
rs776745444 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78825404 | AGCTCACCATTGGTG[C/T]CATTCTTATTTTTTC | 57602 |
rs776753800 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78825731 | GGGGTCAGTTTCTGT[A/C]CTAAGAGCGCTCCAG | 57602 |
rs776779282 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78816821 | ATTTGTTGAAATGCA[C/T]AGATCTTCAGTATAT | 57602 |
rs776783410 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807457 | CTTTCCAGGGTCGTC[C/T]AGGATGGTTGGCATG | 57602 |
rs776815586 | snp | C/G/T | 0.0021281 | 0.0325507 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806992 | CAGTTTTTTGGCTGG[C/G/T]GGAGGAGACATGGTG | 57602 |
rs776837620 | snp | A/G | 1.64811e-05 | 0.00287059 | stop-gained, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813774 | CGTGAGTTTATTACC[A/G]CAGATAGAACAGCAC | 57602 |
rs776872958 | snp | A/G | 3.31983e-05 | 0.00407407 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835400 | GTCCTGCGCCCACGC[A/G]GAAGACCCGCTCCCA | 57602 |
rs776875112 | snp | A/G | 6.76819e-05 | 0.0058169 | intron-variant | USP36 | GRCh38.p7 | 17:78820950 | TCACCCTCTGGCCTC[A/G]CTCTCCTACTGCAAA | 57602 |
rs776914038 | snp | A/C/G | 0.000148476 | 0.00861504 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806253 | GGGGAGGTGGACGGA[A/C/G]GTCATTGCCGGTCGC | 57602 |
rs777030818 | snp | A/C | 1.6676e-05 | 0.00288751 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807218 | CTGGAGCTGCTGGAG[A/C]CCCTCCTGTCGAGGC | 57602 |
rs777053299 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822613 | CCGCTCACTAACTGG[G/T]ATCTGAGGCACTCTG | 57602 |
rs777064054 | snp | C/T | 3.34348e-05 | 0.00408855 | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836402 | AGAAACATAGAGCCA[C/T]AGATAACGAAATCCC | 57602 |
rs777066797 | snp | G/T | 0.000131776 | 0.00811608 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798954 | TCAACCACGGTCTCA[G/T]TCCGGGCCTGTCTGC | 57602 |
rs777078952 | snp | A/G | 1.68898e-05 | 0.00290596 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803644 | CTGTGTCCTCCGGGC[A/G]CTTCTTCTTCTTCCT | 57602 |
rs777170545 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78794023 | TACTTGGCCTCCGAA[C/T]CCAACTAACCACCCT | 57602 |
rs777191172 | snp | A/G | 6.65192e-05 | 0.00576673 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807193 | GTCGCTGCTGGCCGA[A/G]TGCTCTGGGCTGGAG | 57602 |
rs777209404 | snp | A/T | 0.000131778 | 0.00811614 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798941 | TTCGTCCCAGTCATC[A/T]ACCACGGTCTCAGTC | 57602 |
rs777212345 | snp | C/T | 2.36605e-05 | 0.00343943 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821023 | CGTCCAAGTAGGGGT[C/T]GTAGGTGTCCGAGAC | 57602 |
rs777219017 | snp | A/C | 1.71129e-05 | 0.00292509 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803654 | CGGGCGCTTCTTCTT[A/C]TTCCTCTTCCTCTTC | 57602 |
rs777237663 | snp | A/G | 2.78726e-05 | 0.00373303 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821051 | GACGCTCTTGCACAC[A/G]GAGCACTTCACTGCA | 57602 |
rs777255941 | snp | C/G | 4.95814e-05 | 0.00497878 | intron-variant | USP36 | GRCh38.p7 | 17:78813019 | GTCAAAGGAAGAAAA[C/G]AAGTAGGGAATTCTC | 57602 |
rs777259741 | snp | C/T | 1.66114e-05 | 0.00288192 | intron-variant | USP36 | GRCh38.p7 | 17:78813048 | TCTTACTAGGCATTA[C/T]AGAAACGGAGAGAAT | 57602 |
rs777349247 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805936 | ACTAAGACATCAGGA[C/T]TGCAGAGGCCGAACT | 57602 |
rs777411928 | snp | C/T | 2.36628e-05 | 0.0034396 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821005 | CCCGGATCTCCAGCG[C/T]GACGTCCAAGTAGGG | 57602 |
rs777422484 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807303 | GGAGCTTAGGTGAGG[C/T]AGAGAGGACAACATC | 57602 |
rs777440425 | snp | A/G | 3.31334e-05 | 0.00407009 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835392 | GTTGTGGAGTCCTGC[A/G]CCCACGCGGAAGACC | 57602 |
rs777476912 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806159 | CCCAAAGCTTACCTG[A/G]CTCTATGGACGGGCC | 57602 |
rs777498509 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78816140 | GTGTGTTTAGGAACT[A/C]CGAAAAACATACGCA | 57602 |
rs777501860 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803540 | ATCTTCCTGCCGTCT[A/G]ACAGCGGGCAGCTGT | 57602 |
rs777519678 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833957 | TTCTTAAAAGTTACA[C/T]AGAAATTGGCTGGGC | 57602 |
rs777551549 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805195 | GAAAACAGGACCCCC[A/G]TCATCATCTAAACAA | 57602 |
rs777551624 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815318 | GCCTCGCAACAGAGC[A/G]AGACTCCATCTCAAA | 57602 |
rs777563065 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78810022 | CAGCTAACTTTTGTA[C/T]TTTTAGTAGAGACAG | 57602 |
rs777618240 | snp | C/T | 2.05653e-05 | 0.00320659 | intron-variant | USP36 | GRCh38.p7 | 17:78804010 | GAAACAGGGAGAGGA[C/T]GTTCTGAAAGACCCA | 57602 |
rs777676047 | snp | A/T | 2.13472e-05 | 0.00326698 | intron-variant | USP36 | GRCh38.p7 | 17:78828851 | TCTCTACAAAAAATT[A/T]AAAAATAAATAAATC | 57602 |
rs777730943 | snp | C/T | | | downstream-variant-500B, intron-variant | USP36 | GRCh38.p7 | 17:78795456 | AACCCGCCTGCGCCC[C/T]GGGGTTCATTCAGCC | 57602 |
rs777774865 | in-del | -/GGG | 1.82207e-05 | 0.00301828 | cds-indel, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803932 | GGGGTGGGGGCTGAA[-/GGG]GGGGGGTTGCAGGCG | 57602 |
rs777775978 | snp | C/T | 1.66682e-05 | 0.00288684 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807240 | TGTCGAGGCCAGCGC[C/T]CTCGTCGTTCCCCTT | 57602 |
rs777776668 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815954 | CACACATGCATGCAC[A/G]CACATATACATACAC | 57602 |
rs777796035 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828447 | CTCCCAGCTCTCCCT[C/T]AGGCCCACCTGCCTG | 57602 |
rs777805491 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800745 | CTGCAAGAGCCCATG[C/T]GGCCCCCAGCGCCTC | 57602 |
rs777808677 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78787511 | AATGTATACATGCTA[C/T]TCGTTTACAGGTGTA | 57602 |
rs777864848 | in-del | -/AAAC | 1.72994e-05 | 0.00294099 | intron-variant | USP36 | GRCh38.p7 | 17:78813904 | ATGTTGCAGAAAACA[-/AAAC]AATCAACAAGCATCC | 57602 |
rs777875546 | snp | C/T | 2.04067e-05 | 0.0031942 | intron-variant | USP36 | GRCh38.p7 | 17:78807673 | ACACAACTGAGGAAG[C/T]GAGAAGTCTCAGCTG | 57602 |
rs777887248 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78823024 | CGTTTCCCACGGCCA[C/G]CCAGACCATTCCACA | 57602 |
rs777887592 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824492 | GAGCCTGCCGTGAGC[-/G]GAGATTGCACCACTG | 57602 |
rs777943978 | snp | A/G | 1.64765e-05 | 0.00287019 | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798410 | CCGACCTCCTTCCAC[A/G]GGGGCACAGTCAGCG | 57602 |
rs777989440 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | USP36 | GRCh38.p7 | 17:78840888 | CGTTCGCGCTGCGCT[A/T]ACTCCGAAAGGGTTG | 57602 |
rs778009516 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78791896 | GGCCAGGATCCTATA[A/C]TGAGGGGGCACCTCT | 57602 |
rs778043489 | snp | A/G | 5.1754e-05 | 0.00508668 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803831 | AGACACAAGGTCCTC[A/G]TTGACCTGAGGCAGC | 57602 |
rs778056753 | snp | A/G | 1.66037e-05 | 0.00288125 | intron-variant | USP36 | GRCh38.p7 | 17:78818821 | ATGAATGATTGATTC[A/G]TGCTCTGAAAAATGT | 57602 |
rs778072599 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78817738 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGA | 57602 |
rs778125694 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78817898 | CCACCCTGGGCAACA[C/T]AGCAAGATGCTGTCT | 57602 |
rs778154235 | snp | A/C | 0.000147395 | 0.00858345 | intron-variant | USP36 | GRCh38.p7 | 17:78827146 | AAGGGCAGCCTGGGT[A/C]GAAAGGTGCCGGGCT | 57602 |
rs778169878 | snp | C/G | 0.00010784 | 0.00734223 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802489 | TTTTCTTTTTCCTTG[C/G]AGACTCTTCCATGGC | 57602 |
rs778203464 | in-del | -/AGG | | | intron-variant | USP36 | GRCh38.p7 | 17:78813371 | GTGACAGCCAGCTCC[-/AGG]AGAAGGCCCCTCCAG | 57602 |
rs778205814 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806888 | AATGTTCTCACTCCC[-/T]TCAAACCACAACCAA | 57602 |
rs778206778 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78791002 | AAGACATGTATCGTG[A/G]GAGTGACAGCTGACA | 57602 |
rs778272120 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814435 | AGCAGTAATAGTGCC[C/T]GGCATGGCAGCTGTA | 57602 |
rs778272808 | snp | A/G | 1.65581e-05 | 0.00287728 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78813865 | CTGGTACCACTGTCC[A/G]TTGCTTGCCTGAAGC | 57602 |
rs778311844 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78804886 | TTATTTTCCAACCTC[C/T]GAAAGTCTCAGGGTG | 57602 |
rs778326904 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814526 | CATATACGGACGTAT[A/G]TTGAGGAATTCCGGA | 57602 |
rs778327038 | snp | A/C | 4.95356e-05 | 0.00497648 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807430 | CTGTGGAGGAGCTGG[A/C]TTCTTCACCTTCTTT | 57602 |
rs778382161 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832467 | AGTGATACTGGCCCA[C/T]GGGACCGGTATTGGA | 57602 |
rs778382579 | snp | A/G | 3.29663e-05 | 0.00405981 | intron-variant | USP36 | GRCh38.p7 | 17:78822014 | TCCAACCTGAAAAGG[A/G]GACCCCAGCCTTTAA | 57602 |
rs778431220 | snp | A/G | 1.72311e-05 | 0.00293518 | intron-variant | USP36 | GRCh38.p7 | 17:78813899 | CAAGGATGTTGCAGA[A/G]AACAAAACAATCAAC | 57602 |
rs778444907 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821981 | TGATGGACCAAGGTA[A/G]TAGCCTGCGTTTGAC | 57602 |
rs778470078 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78831733 | GGATCGCTGAGCCCA[C/G]GTGTTTGAGACCAGC | 57602 |
rs778484818 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78837705 | TCACAATTTCAAAAA[C/T]ATGTCCCTTAAATTG | 57602 |
rs778504905 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | USP36 | GRCh38.p7 | 17:78799029 | CAGGTCAGAACTACC[A/G]GGCAGACACGGGGGT | 57602 |
rs778576275 | snp | A/C | | | intron-variant, missense | USP36 | GRCh38.p7 | 17:78823131 | GGCACTTCCCAGACT[A/C]CGGGAGCTCTGAAAT | 57602 |
rs778590485 | snp | A/G | 3.8675e-05 | 0.00439727 | intron-variant | USP36 | GRCh38.p7 | 17:78821085 | GAACAGAGGCAGTGG[A/G]GCAGGTGGGGCCTGG | 57602 |
rs778609868 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806220 | TCATGGGGTGGGTGA[C/G]GTCGGAGGATGGTGA | 57602 |
rs778670762 | in-del | -/GGC | | | intron-variant | USP36 | GRCh38.p7 | 17:78831122 | CCCAGCTACTCGGGA[-/GGC]GGCTGAGCCAGGAGA | 57602 |
rs778681717 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78820326 | CAAAGAAATTTAAAA[A/T]ATTAGCCAGGCGTGG | 57602 |
rs778698742 | snp | A/G | 1.84232e-05 | 0.003035 | synonymous-codon, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78802511 | TTCCATGGCCTCTGG[A/G]TCACCATCACCCATG | 57602 |
rs778714947 | in-del | -/TCTTTTTTTTTT | | | | | GRCh38.p7 | 17:78791128 | TTCCCAATCTGGCCT[-/TCTTTTTTTTTT]TTTTTTTTTTTTTAG | 57602 |
rs778721740 | snp | A/C | | | | | GRCh38.p7 | 17:78797922 | CAGAGAGAAACGAGA[A/C]CCGAATCTTCCCACT | 57602 |
rs778741741 | snp | C/G | | | | | GRCh38.p7 | 17:78788401 | ATCTCTTGACCTCGT[C/G]ATCTGCCTGCCTCGG | 57602 |
rs778769762 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78829259 | TCACCATCACAACCT[A/C]ACACCATCACCCCAC | 57602 |
rs778791824 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793066 | CCTAAGCCTCACCCA[C/T]AGATTCTGATTCTAC | 57602 |
rs778822043 | snp | C/T | 1.65078e-05 | 0.00287291 | intron-variant | USP36 | GRCh38.p7 | 17:78819884 | GGTGAGGGGACTTAT[C/T]TCCCGTCTGGTATCA | 57602 |
rs778856092 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78820089 | TGCCAAATTTAAGGT[A/C]TTTTTTAGGCTGAGG | 57602 |
rs778884705 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78805760 | CCACAAAAAACGCTC[A/G]GGACTCCGAGCTCAC | 57602 |
rs778887484 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793895 | ATGCCTAGGATTCTC[C/T]CTGGGTTCCCTGTAC | 57602 |
rs778903876 | in-del | -/GC | 1.70621e-05 | 0.00292074 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78835284 | CCCACACTCACAGCT[-/GC]GAGCATGCTCCTTGG | 57602 |
rs778930152 | snp | C/G/T | 3.33657e-05 | 0.00408436 | intron-variant | USP36 | GRCh38.p7 | 17:78828887 | AATTTTAACATGGAT[C/G/T]GATGCTTACTTTTCA | 57602 |
rs778944901 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836259 | GATTTTCTGTAAAAG[A/G]ACCTTCTTGGCAGAG | 57602 |
rs778959912 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812871 | ATACCTTTCCAGTCA[A/G]TGGGGAGGAAATAAT | 57602 |
rs778976054 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78798503 | GAAGTTTCTGGAAGG[C/T]GTTGAAGTTTCTCCT | 57602 |
rs779010244 | snp | A/G | 5.1935e-05 | 0.00509557 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803847 | TTGACCTGAGGCAGC[A/G]CCGTCGAGATGGAGG | 57602 |
rs779023529 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78806384 | ATGAAAATAAAAACA[A/C]AAGAGCCCAGAAAAA | 57602 |
rs779031841 | snp | A/G | 0.000133111 | 0.00815708 | intron-variant | USP36 | GRCh38.p7 | 17:78827166 | GGTGCCGGGCTGGCT[A/G]TTGCCATAGGAATGT | 57602 |
rs779056597 | snp | C/T | 3.3432e-05 | 0.00408838 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78828987 | GCATGACACACAGCA[C/T]GCAGAAGCTTCCCTG | 57602 |
rs779066331 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789774 | GTTCACTTCAAATAG[A/T]GGAGCTAGTGCTCTA | 57602 |
rs779121096 | snp | C/T | 5.299e-05 | 0.00514705 | intron-variant | USP36 | GRCh38.p7 | 17:78835275 | TGCTGCAAACCCACA[C/T]TCACAGCTGCGAGCA | 57602 |
rs779125282 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78817713 | ACTGCAATCCAGCCT[A/G]GGCATCAGAGCAAGA | 57602 |
rs779150729 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800873 | GGACCCTGGCGCACC[C/G]CAAGTGCTCAAGTGA | 57602 |
rs779155804 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824633 | AGAAATAAAGAAAAA[C/T]CAGAAATAAGCACAG | 57602 |
rs779184716 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816742 | TCAGCCTCCCTAAGT[A/G]CTGACATTAGAGTTG | 57602 |
rs779188460 | snp | A/G | 0.000100518 | 0.00708863 | intron-variant | USP36 | GRCh38.p7 | 17:78802296 | GGTGCACACCCATGC[A/G]GTTCCCACCCCCTCG | 57602 |
rs779252612 | snp | G/T | 0.00148843 | 0.0272396 | intron-variant | USP36 | GRCh38.p7 | 17:78827226 | AAAGCCCTGGGAGGG[G/T]GGGTGGGGAAGCACG | 57602 |
rs779254803 | in-del | -/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78805383 | GCTTGTGTGTGTATA[-/T]GTGAGAGGAGAGTAA | 57602 |
rs779257288 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78809978 | CGGCCTCTCGAATAG[C/T]TGGGATTACAGGCGC | 57602 |
rs779289271 | snp | C/T | 4.97006e-05 | 0.00498476 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814546 | GGAATTCCGGATAGC[C/T]TACATCCTGTTTGAA | 57602 |
rs779348965 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78799402 | CCCTTCCCTACCCAA[G/T]ACACAGCATGTGTGG | 57602 |
rs779404823 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78819852 | CTAAGGAAGAGTGGG[C/T]GGGCACAACACTGTC | 57602 |
rs779409830 | snp | C/T | 1.73709e-05 | 0.00294706 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78829007 | AAGCTTCCCTGGTGG[C/T]CTGCCGGCGTGGAAG | 57602 |
rs779422397 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814449 | CCGGCATGGCAGCTG[G/T]AGCCCGAGTGCACCA | 57602 |
rs779425142 | snp | A/C/T | 4.98594e-05 | 0.00499276 | intron-variant | USP36 | GRCh38.p7 | 17:78799776 | GCTCAGCCCTGCAAT[A/C/T]GGAGCAGCCAAGAAA | 57602 |
rs779426655 | snp | G/T | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807417 | TGGGGGAAAAGTGCT[G/T]TGGAGGAGCTGGCTT | 57602 |
rs779463606 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78813352 | GTCTCCAGCCTCCAG[A/G]TCAGTGACAGCCAGC | 57602 |
rs779509829 | snp | A/C | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841725 | TAAACTACTTTATCC[A/C]AAAGGCAGAACTTTG | 57602 |
rs779514952 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78835097 | ACAGCCCCACCTGAC[C/T]GATTCACCTTCATGG | 57602 |
rs779537628 | snp | C/G | 6.59087e-05 | 0.00574021 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806184 | CGGGCCAAGTGGAGG[C/G]AACGACGGGGTGAGA | 57602 |
rs779588166 | snp | C/T | 1.65321e-05 | 0.00287502 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78814417 | AGCCTCTCACCTTCA[C/T]GTAGCAGTAATAGTG | 57602 |
rs779592769 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78806228 | TGGGTGAGGTCGGAG[C/G]ATGGTGAGGGGGGAG | 57602 |
rs779609241 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78812614 | AGAATGGCGGGAACC[C/T]GGGAGGCAGAGCTTG | 57602 |
rs779630970 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78822313 | ACGTGTATCCTCACC[C/T]AGTGTTGCCTTTTCT | 57602 |
rs779717121 | snp | A/G | 3.34018e-05 | 0.00408654 | intron-variant | USP36 | GRCh38.p7 | 17:78813876 | GTCCATTGCTTGCCT[A/G]AAGCAGCCAAGGATG | 57602 |
rs779734062 | in-del | -/CT | 3.29489e-05 | 0.00405874 | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836160 | GTGGCGACTAGCTCC[-/CT]CTGTTTTGGGGTTGA | 57602 |
rs779746607 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78802959 | TTTTTCTTTTTTTTT[-/A]AGACAGGGTTTAGCT | 57602 |
rs779767309 | snp | G/T | 0.000149371 | 0.0086408 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803519 | ATTCACCTGTGGCTG[G/T]GTGCCATCTTCCTGC | 57602 |
rs779770423 | snp | A/G | 4.95683e-05 | 0.00497812 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807332 | TCCCTGCTGTCCCAG[A/G]AGCCCTGCCTTTGGC | 57602 |
rs779790679 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78829706 | AGTCTGCCCACCCCT[A/G]CGCTACATAAAACGC | 57602 |
rs779813827 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78828320 | CAGATTTCAAAAACC[A/G]GTAATAGGCCTCTTC | 57602 |
rs779817612 | snp | C/G | 1.65045e-05 | 0.00287263 | intron-variant | USP36 | GRCh38.p7 | 17:78819891 | GGACTTATTTCCCGT[C/G]TGGTATCAGTCTTCT | 57602 |
rs779822963 | snp | A/T | 1.65015e-05 | 0.00287237 | splice-donor-variant, intron-variant | USP36 | GRCh38.p7 | 17:78799665 | TGTCTCCAAATCAGT[A/T]CCTTTTCTCCCGTAA | 57602 |
rs779829495 | in-del | -/T | 1.6537e-05 | 0.00287545 | intron-variant | USP36 | GRCh38.p7 | 17:78820065 | GAGGAAAAAGGCTGA[-/T]TCAAGAAATGCCAAA | 57602 |
rs779840963 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78793007 | AGGTGTGAGCCACCG[C/T]GCCCGCCCCCCTCAC | 57602 |
rs779861235 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78812718 | AAAAAAAAAAAAAAA[A/G]GAAAAGAAAAGAAAT | 57602 |
rs779925543 | snp | A/C | 3.29511e-05 | 0.00405887 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836183 | TGGGGTTGAGCAACA[A/C]ATATTTGCTCTTTAA | 57602 |
rs780000218 | snp | C/T | 1.6628e-05 | 0.00288335 | missense, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78803413 | GGTCCTGGTGCAGGC[C/T]GCCTTCTTCACCAAG | 57602 |
rs780033044 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78804317 | AAATACAAAATTAGC[A/C]GGGCGTGGTGGCACA | 57602 |
rs780035370 | snp | C/T | 6.59609e-05 | 0.00574248 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78812985 | GGCCCTCGGGACTTT[C/T]CTTAGAGCCTGGAAT | 57602 |
rs780036967 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78792260 | GGAGATGCCTGAACA[C/T]GTTCCTAAGGGAAGA | 57602 |
rs780054297 | snp | A/C | 8.24355e-05 | 0.00641957 | intron-variant | USP36 | GRCh38.p7 | 17:78820025 | TTGCTGAGGAGGACA[A/C]AAACAGGGAGTAAAA | 57602 |
rs780073439 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836272 | AGGACCTTCTTGGCA[A/G]AGGAGGCAAGAAGCT | 57602 |
rs780077253 | snp | A/G | 5.07825e-05 | 0.00503872 | missense, utr-variant-5-prime, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78827294 | CGTCGATGGTGTACC[A/G]CAGGAACTCATGCGC | 57602 |
rs780083507 | snp | C/T | 1.6793e-05 | 0.00289763 | intron-variant | USP36 | GRCh38.p7 | 17:78814565 | ATCCTGTTTGAAAAA[C/T]CAAGGAAAAGACAAA | 57602 |
rs780116907 | snp | A/G | 1.75718e-05 | 0.00296405 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803897 | CGTCCCTGGGGGCTT[A/G]GGGGTACTGGACAGC | 57602 |
rs780159854 | snp | C/T | 3.46572e-05 | 0.00416262 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803852 | CTGAGGCAGCGCCGT[C/T]GAGATGGAGGAGCAG | 57602 |
rs780201704 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78833219 | TAACCTTTGCTGCTA[C/T]GAAGCCATCGCAATT | 57602 |
rs780224522 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78815353 | TCAAAACAAACAAAC[A/G]AAGAAAAAACACCAA | 57602 |
rs780241516 | snp | C/T | 0.00051966 | 0.0161109 | intron-variant | USP36 | GRCh38.p7 | 17:78802313 | TTCCCACCCCCTCGC[C/T]CGGTGCATACCCATG | 57602 |
rs780275432 | snp | A/G | 1.66457e-05 | 0.00288489 | intron-variant | USP36 | GRCh38.p7 | 17:78806951 | CGGCGAGACCCCCAC[A/G]CACCCACCTTCTTGG | 57602 |
rs780287611 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78824374 | GGAGCGAGGAAAACA[C/G]GACCAGGTGCATTTC | 57602 |
rs780293629 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78818880 | CAACTGCTCTGTAAT[A/G]GTGGAATCTTCATCA | 57602 |
rs780295112 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78832575 | AACTGCAGCTTACCT[A/G]TGCCAGGTTACGGGG | 57602 |
rs780354663 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78806735 | CTCCATGAGTCACAT[A/G]AGCATCACCAGATCA | 57602 |
rs780437019 | snp | C/T | 1.7306e-05 | 0.00294155 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807566 | AGGCCCAGGGTGGAG[C/T]CATTCCTGGATATGG | 57602 |
rs780446860 | snp | C/T | 3.32033e-05 | 0.00407438 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807180 | GGGCCTTGGTGGAGT[C/T]GCTGCTGGCCGAGTG | 57602 |
rs780488083 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78789704 | TGTATCCAGCTGTCA[C/T]CAACTGTTCCCTGTG | 57602 |
rs780509758 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78788321 | AGGTATGCGCCACCA[C/T]GCCCAGCTGATTTTT | 57602 |
rs780519181 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807047 | CTCAGGACAGGGGAC[C/T]TCAGCTTCACCGTCT | 57602 |
rs780533479 | snp | C/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78799855 | TAAATTATAAAACAA[C/G]TTACAGTAAGTGGAT | 57602 |
rs780535325 | snp | A/C | 3.29919e-05 | 0.00406138 | intron-variant | USP36 | GRCh38.p7 | 17:78820039 | AAAAACAGGGAGTAA[A/C]ATACACAGCAGAGGA | 57602 |
rs780594187 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78806030 | ACGCCCCCCTGTACC[C/T]CCTGGCTGCCCCAAT | 57602 |
rs780610441 | snp | A/C | 1.69026e-05 | 0.00290706 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803648 | GTCCTCCGGGCGCTT[A/C]TTCTTCTTCCTCTTC | 57602 |
rs780636071 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78828566 | CAGCCCACATGTCTC[C/T]AAACTGCTATTCCTT | 57602 |
rs780757747 | snp | G/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78830074 | CCTTTCAAATTATGA[G/T]GTAAATAAACACTGC | 57602 |
rs780783772 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820892 | AGGAGTTTTCTCCCT[A/G]TCTATTTTGATCTGA | 57602 |
rs780973114 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78802034 | TCAGATGCAGTAGAC[A/G]CTGCTCTCAGCCTGT | 57602 |
rs781016935 | snp | G/T | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807480 | TTGGCATGTGTGTGG[G/T]TGTCTGGGAGAGTTT | 57602 |
rs781061787 | snp | C/T | | | utr-variant-3-prime, intron-variant | USP36 | GRCh38.p7 | 17:78795661 | CAGAACTCACAAAAC[C/T]GGAGTATTTTATTGC | 57602 |
rs781132569 | snp | G/T | 9.8464e-05 | 0.00701586 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78820996 | AGATCTGTACCCGGA[G/T]CTCCAGCGCGACGTC | 57602 |
rs781183155 | snp | A/C/G | 3.57999e-05 | 0.00423068 | missense, synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803921 | GGACAGCAATGTGGG[A/C/G]TGGGGGCTGAAGGGG | 57602 |
rs781206395 | snp | A/C | 4.95438e-05 | 0.00497689 | intron-variant | USP36 | GRCh38.p7 | 17:78813007 | GCCTGGAATTCTGTC[A/C]AAGGAAGAAAACAAG | 57602 |
rs781220749 | snp | G/T | 1.66391e-05 | 0.00288431 | synonymous-codon, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803624 | CTCCTGCAGGGCGCT[G/T]GCAGCTGTGTCCTCC | 57602 |
rs781230007 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78826487 | CTTATTTACGTAAGA[A/G]TATCATCCACTGAGG | 57602 |
rs781231706 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78820588 | GGTTGGCCCAGCAAA[A/G]GCAGACCACCCTCCC | 57602 |
rs781259744 | snp | A/C/G | 3.29784e-05 | 0.00406058 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78836310 | TTCTCCATCATCAGC[A/C/G]GAGTCCTTGCGGCCG | 57602 |
rs781290121 | snp | C/G | 0.000114699 | 0.00757206 | intron-variant | USP36 | GRCh38.p7 | 17:78807641 | GAGTCTTGTCGCTAA[C/G]GAGACCAAAGCAGAA | 57602 |
rs781309073 | in-del | -/C | 0.000137306 | 0.00828457 | frameshift-variant, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803776 | CTTCTCAGAGGGGCT[-/C]CTGGGGGGGCTCACT | 57602 |
rs781316165 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78839482 | AAAAACTCCCCACAA[C/T]ATCACTGCTTTCGGT | 57602 |
rs781347871 | snp | A/G | 1.70583e-05 | 0.00292042 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | USP36 | GRCh38.p7 | 17:78803722 | GGAGGCGCGTCTCTG[A/G]GCCCAGCCTCTGCGG | 57602 |
rs781409034 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78832503 | GACCAGGCGTTCCCC[A/T]TGAAGGGATGGCCAT | 57602 |
rs781431010 | snp | A/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78842291 | GAGACTCCGTCTCAA[A/G]AGAAAAGAAAAGAAA | 57602 |
rs781489776 | snp | A/G | 4.6788e-05 | 0.00483651 | intron-variant | USP36 | GRCh38.p7 | 17:78827381 | GGGAGGGAAGAGCTC[A/G]TGTCTTCTCATCAAA | 57602 |
rs781545937 | in-del | -/TTTT | | | intron-variant | USP36 | GRCh38.p7 | 17:78800971 | ATGTTAGGGCAGTAT[-/TTTT]TTTTTTTTTTTTTTT | 57602 |
rs781557175 | snp | A/G | 3.29723e-05 | 0.00406018 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807101 | GTTTTGGAGTGGCCA[A/G]CGGTGGAACAGTTCG | 57602 |
rs781572520 | snp | C/T | 8.23744e-05 | 0.0064172 | synonymous-codon, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78807058 | GGACTTCAGCTTCAC[C/T]GTCTTAGAATCTGCT | 57602 |
rs781603055 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78823207 | TTAGAAAATGAAAAA[C/T]CAACTGCCACCATCT | 57602 |
rs781645213 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78797655 | GTGTGCGGCCACCTC[A/T]GCTCACACACACACT | 57602 |
rs781661637 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | USP36 | GRCh38.p7 | 17:78821990 | AAGGTAGTAGCCTGC[A/G]TTTGACGATCCAACC | 57602 |
rs781677253 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800349 | ACCTCCTAAGCCCTG[C/T]CCAGGGGGAACCTGG | 57602 |
rs781698069 | snp | A/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78824265 | TGCCAACAAAAAAAA[A/T]GAAATCATGCACGCT | 57602 |
rs781712707 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78798609 | CTTTCCTGGCCCACG[A/G]GGCTCCATGCTGCAT | 57602 |
rs781721282 | in-del | -/TGGAGTGCAGTGG | | | intron-variant | USP36 | GRCh38.p7 | 17:78801024 | CTCTGTCACCCAGGC[-/TGGAGTGCAGTGG]CGCAATCTCGGCTCA | 57602 |
rs796120153 | in-del | -/ATAT | | | intron-variant | USP36 | GRCh38.p7 | 17:78835018 | TATATATATATATAT[-/ATAT]TTTGGAAGTATCTTT | 57602 |
rs796157959 | in-del | A/GAGACC | | | intron-variant | USP36 | GRCh38.p7 | 17:78813270 | ACCAGAAAGCAAGAA[A/GAGACC]CTCAAACACCTCAGC | 57602 |
rs796237192 | in-del | -/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78810117 | TCCCAAAGTGCCCGG[-/C]CCCCCTCTTCTTTTT | 57602 |
rs796251939 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78831647 | CCTCTAATCATTATA[C/T]ATAAAACGCTGCTGG | 57602 |
rs796362611 | in-del | -/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78816348 | AAAATTTTTTAGGCC[-/G]GGCATGATGGCTCAC | 57602 |
rs796370643 | snp | C/G | | | upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78841761 | ACAGTCGTATCTGCT[C/G]TGTCTTTTTTGATGT | 57602 |
rs796482769 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78815849 | TACATACACACACAC[-/AT]ATGCATGCATACACA | 57602 |
rs796587292 | snp | A/G | | | intron-variant | USP36 | GRCh38.p7 | 17:78800775 | CCTTGCTGAGCATGA[A/G]CCCTTACTGTGTGGT | 57602 |
rs796623280 | in-del | -/AT | | | intron-variant | USP36 | GRCh38.p7 | 17:78835017 | TATATATATATATAT[-/AT]TTTGGAAGTATCTTT | 57602 |
rs796646108 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78791740 | GGAGACTATTTTCTC[C/T]GAACAGGAGTGAGAA | 57602 |
rs796709957 | snp | A/C | | | intron-variant | USP36 | GRCh38.p7 | 17:78828648 | TTCATCCATGACTCA[A/C]TCTTCTCTCCCTTCT | 57602 |
rs796778617 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP36 | GRCh38.p7 | 17:78836799 | GTTATACACACACGG[-/AC]ACACACACACACACA | 57602 |
rs796811301 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78800652 | TGCAGAGCAGCCTGC[C/T]TGCTCCCAACGTGCT | 57602 |
rs796826751 | in-del | -/A | | | intron-variant | USP36 | GRCh38.p7 | 17:78821414 | TATATATATATATAT[-/A]TATATATTTTTTTTT | 57602 |
rs796939882 | snp | C/T | | | intron-variant | USP36 | GRCh38.p7 | 17:78834977 | CAGAGCAAGATACTG[C/T]CTCTAAAAAAATAAT | 57602 |