SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs112998860 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938579 | AGGCAGGCAGATCAC[C/T]TGAGGTCAGGAGTTC | 55833 |
rs113002616 | snp | C/T | 0 | 0 | utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34048922 | CGGCGGCACAGGCTG[C/T]CCAACCCGTCACGTG | 55833 |
rs113043058 | snp | A/C | | | splice-acceptor-variant | UBAP2 | GRCh38.p7 | 9:33986838 | TTTCTTCACCTCTAA[A/C]TAGGGGGAAAAGAGC | 55833 |
rs113048300 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035268 | AGCACTTTGGGAGGC[A/C]GAGGCGGGCGGATCA | 55833 |
rs113089243 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970575 | AGCTGGGACCACAGG[G/T]GCACACCACCATGCC | 55833 |
rs113144103 | snp | C/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036287 | ATGCCCGGATAATTT[C/T]TTATAATTTAATAGA | 55833 |
rs113191948 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986199 | CTGGGACTACAGGTG[C/T]GTGCCACCACACTTA | 55833 |
rs113214434 | in-del | -/T | 0.407674 | 0.194008 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949195 | ATAAATAAATAAAAA[-/T]AAAATAAAATAATAA | 55833 |
rs113218757 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964077 | TCTAATCTGTTCAAC[A/G]GGTACCAGTTTTTAG | 55833 |
rs113312647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976962 | AGTCGCAGTGAGCCG[A/T]GATGGCGCCACTGCA | 55833 |
rs113349289 | snp | A/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951771 | ACTACATAAAGCAAC[A/G]TATCTGAAGATTGCT | 55833 |
rs113358451 | snp | A/C | 0.0562307 | 0.157967 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046612 | TCAGGCCACTGCACT[A/C]CAGCCTGGGCGACAG | 55833 |
rs113373463 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981284 | ATATATATATTCTGG[A/T]TATATATATATATTC | 55833 |
rs113378294 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042346 | AGCCAGGCGTGGTGG[C/T]GGGCACCTATAATCC | 55833 |
rs113389114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996049 | ACGACTTCATGAAGA[A/C]ACCATACATAACAAA | 55833 |
rs113398133 | snp | A/G | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983460 | GTAAGAGGGGAAGAA[A/G]CTGGGTTACTATGTA | 55833 |
rs113457187 | snp | A/C | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034511 | TCCAGTTTTAATCCA[A/C]ATACAAAATTCCTTA | 55833 |
rs113462606 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975283 | AAAAAAATGCAAAAA[A/T]TAGCCAGGCGTGGTG | 55833 |
rs113580742 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045171 | CTAACACTGTGAAAC[C/T]CCGTCTCTAATAAAA | 55833 |
rs113608424 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929215 | TACTTGGATATATAC[A/T]ACCTTTTAATCTCGG | 55833 |
rs113620880 | snp | A/G | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923522 | TGTAGGAAGAGGCAA[A/G]CTGAGGCTGGTCAGG | 55833 |
rs113643627 | snp | C/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050277 | CCCGGCATGCCTTAT[C/G]TCAATTGGAGCTTTC | 55833 |
rs113689970 | snp | C/G | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030479 | AACAAAAAAACTGGC[C/G]CGGTATGACAGAGCA | 55833 |
rs113748484 | snp | A/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947997 | AAAAAAAAAAAAAAA[A/T]AAAAAAGTCTTAAAA | 55833 |
rs113749838 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931872 | TCCTGTTGTCCAGGA[A/G]CATGCACTTTTTGTT | 55833 |
rs113769339 | snp | G/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998516 | TCGGAAAACCTCAGT[G/T]TGCTTACAGAAATGT | 55833 |
rs113784973 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040788 | ACTCTGTGTATAAGC[C/T]GAACTTTTTCCAGAC | 55833 |
rs113799738 | in-del | -/A | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040160 | GCTAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 55833 |
rs113809631 | snp | A/G | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933118 | GCCATGGAAAGTTCA[A/G]GTCAGACACCTGCTC | 55833 |
rs113822491 | snp | C/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020448 | TCCTGTCTCAGCCTC[C/T]CGAATAACTGGGACC | 55833 |
rs113824960 | snp | C/T | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955550 | AACAAAAAAAAGGGC[C/T]AGGTGTGGTGGCTCA | 55833 |
rs113853037 | in-del | -/TA | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976844 | CTACTAAAAAAAATG[-/TA]TATATATATATACAA | 55833 |
rs113876479 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025978 | CTTAACTGAAAATGG[C/T]TGACTTAACAACCAC | 55833 |
rs113937825 | in-del | -/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012840 | ATTTTTTTTTTTTTT[-/T]AAATTGAGGTTCACG | 55833 |
rs113942816 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017929 | GAGACTCCGTCTCAA[A/G]AAAAAAAAAAAATTG | 55833 |
rs114210374 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035961 | TGCAGTGAGCCTGAT[A/C]GCATCACTGCATTCC | 55833 |
rs114212719 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977594 | GCGAATAAACCATAT[G/T]ATGGTAAATGCTGTA | 55833 |
rs114292003 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013012 | TACTAAAATTAGCCG[A/G]GTGTGGTGATGTACA | 55833 |
rs114388719 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938423 | GACATAAGCCACCAT[A/G]CCCAGCCCAACATGA | 55833 |
rs114420687 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926413 | TTCATGTTTCCCAGG[A/G]ATGAGCACTGGATAC | 55833 |
rs114420895 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981557 | AAAAAGCCTGCTACA[C/T]TGTCCACTCTGATCT | 55833 |
rs114466686 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961773 | GGGAAGAGGAGGAGC[A/G]TGCTTGTGAGACAAA | 55833 |
rs114585749 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030010 | AAAAAAGAAAGAAAT[A/G]CATACATAGGCCAGG | 55833 |
rs114758158 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980844 | CCCAGCTACTAGGGA[C/T]GCTGAGGTGGGAAGA | 55833 |
rs114794776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927274 | CCACCACACTGAGGT[G/T]GTTTCAACGTCAGAG | 55833 |
rs114914366 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005578 | AGTCTAAACTACAAG[G/T]AATATAAAACTTAAC | 55833 |
rs114980038 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034022 | ATTAAAGGCATGACC[C/T]ACCACGCCCGGCTTC | 55833 |
rs114980786 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036434 | GATACTTGATTCTAT[A/T]GGAAGAATCTAAGAA | 55833 |
rs115012892 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998979 | ACTAAGTAACAACAA[A/G]TAAAAGACAGTGAAT | 55833 |
rs115049314 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992665 | TCGGGCGGAGGGGGG[G/T]GGGCACAAATAGGGA | 55833 |
rs115118998 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945808 | CTAGTACACATAGGT[A/G]TCATTTTATAAAACC | 55833 |
rs115135297 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043589 | CATAGCTCACTGTGG[A/C]CTCAAGCAATCCTCC | 55833 |
rs115247750 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964637 | CCCAGGAGTTTGAGG[A/T]TGTAGTGCACTAAGA | 55833 |
rs115323515 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992854 | TTATCGGTATTTTGC[C/T]AGTTGCAGAACAGGT | 55833 |
rs115344416 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974008 | GCCAGGAGTTCAAGA[A/C]CAGCCTGGGCAACAT | 55833 |
rs115346846 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007615 | GTTTATTGAAATGAT[C/T]ATATGTTTTTTGTCC | 55833 |
rs115475149 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042718 | TTGGGAGCTGGCATA[C/T]ACAGGAGACTTCCAG | 55833 |
rs115635990 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972461 | AGGCAGAAGGCAGAT[C/T]GCATGAGGCACCACT | 55833 |
rs115676423 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045368 | AAGGGTAGAAAAAAA[C/T]AAAAATTAAAAAAAA | 55833 |
rs115677827 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011478 | GTGCTAGCATATTTA[C/T]GAAAATAAATTTTAA | 55833 |
rs115850036 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031115 | AAACCCTCTCTCTAC[C/T]AAACATACAAAACTT | 55833 |
rs115898409 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988163 | ATATATTAATATAAA[A/G]TATTTTATTTTCTTT | 55833 |
rs115925851 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042457 | CACTTCAGCCCAGGC[A/G]ATAGTGCAAGACTCC | 55833 |
rs115988619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943077 | TAAAATGTGGTATTA[C/T]CAACACAATGAAATA | 55833 |
rs116080596 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045746 | GCAGGAAATATCAGC[A/C]TAAGTGGTTTACATT | 55833 |
rs116160521 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945431 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 55833 |
rs116177892 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972549 | CTTTTCTTGGAGCCA[A/G]TTCCTTTCCTTGACT | 55833 |
rs116195421 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048055 | GTGACAGTTGAGATG[C/T]GTGGGCAACTAATTA | 55833 |
rs116231994 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949336 | CCTAGTCTGTGAACC[A/G]CAGTCTTCATCTTTA | 55833 |
rs116270419 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968652 | TTTCTCCTTAATTTT[A/G]TTAAATGGATAATAC | 55833 |
rs116326562 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963667 | ATAAAAAATGAAAGA[C/T]ATTGCAAGCAATTTA | 55833 |
rs116335299 | snp | C/G/T | 0.00637439 | 0.0561611 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047103 | CCCATGCCACCACTT[C/G/T]CGGGCATATTTCAAT | 55833 |
rs116413805 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030481 | CAAAAAAACTGGCCC[A/G]GTATGACAGAGCACA | 55833 |
rs116469383 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934998 | TATCCGCACTCCCAG[A/G]AAATCCTATTTAAAG | 55833 |
rs116470910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948773 | AACTGACTAAATAAA[C/T]GCAGCTATCCTTCCT | 55833 |
rs116689387 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988852 | ATGGAAACTAAGAAA[A/G]AATTTGAGAAAGCTG | 55833 |
rs116934553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973536 | TTTAAAATCAGAAAG[A/G]GCTAACACCATGGAA | 55833 |
rs116990828 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924138 | CAGCTTGCTGTTGCT[A/G]CTTCCCAGCTCCTGG | 55833 |
rs116999205 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984261 | AGCATTAAGGAAGTA[C/T]CATCTAAGAAATTTG | 55833 |
rs117085691 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024712 | GATAAAGCCAGGCGC[A/G]GTGGCTAATGCCTGT | 55833 |
rs117143878 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955090 | AACTAGTAGAACTCA[A/T]ATAAAATAAGAGATC | 55833 |
rs117160815 | snp | C/T | 0.000115332 | 0.00759293 | missense | UBAP2 | GRCh38.p7 | 9:33922976 | CTCACCTGTGTCTTA[C/T]TGTAGACAGAACCAG | 55833 |
rs117221323 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999796 | GACTGTGCAACCTCC[A/G]CCTCCCAGGCTTAAC | 55833 |
rs117225695 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049473 | CCGCCCGCCATGTGG[C/T]GGAGCGTGGTGCCTG | 55833 |
rs117265931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974274 | GCACTTTGGAACACC[A/G]AGGCAGTTGGACTGC | 55833 |
rs117275412 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047090 | GGCCTCATTCTCTCC[C/T]ATGCCACCACTTTCG | 55833 |
rs117383017 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001288 | CAGGACATACATACA[A/T]ACACATACTAGGGTA | 55833 |
rs117505450 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009112 | GTTTTGTTTTGTTTT[G/T]TTTTTGAGACAGAAT | 55833 |
rs117537664 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982259 | AACCCAAATCCTTTG[C/T]AAAAATCCTCAATTA | 55833 |
rs117553005 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999258 | AAGCACTGCTTGAGC[A/C]CAGGAGTTCGAAATT | 55833 |
rs117642732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019905 | GGTGGCTCATATCTG[C/T]AATCCTAACACTTTG | 55833 |
rs117643251 | snp | A/C | 0.0818113 | 0.184966 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003248 | GTTGGTCAGGCTGGT[A/C]TTGAACGTCTGACCT | 55833 |
rs117686955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024574 | AAACAGGTTTCGCAC[A/T]ACAATCACAGGGGAT | 55833 |
rs117703548 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041199 | GGCTAACACCTGTAA[C/T]CCCGGCACTTTGGGA | 55833 |
rs117724620 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984397 | GCTGGGCATAGTAGC[G/T]CACACCTGTAATCCC | 55833 |
rs117733169 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938101 | TTCCTGGTTCAAGCC[A/T]TCCTCCCACCTCAGC | 55833 |
rs117734439 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012187 | TCACATAAATTCACA[A/G]GAGAGTTGACATCTG | 55833 |
rs117789751 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006637 | GCAGTGAGCATGACC[A/G]TGCCACTGCACTCCA | 55833 |
rs117810673 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962350 | AATTCAGGAGACATA[G/T]TAAAAGTTTAAAAAA | 55833 |
rs117845042 | snp | C/T | 0.0118577 | 0.0760806 | missense | UBAP2 | GRCh38.p7 | 9:33941704 | CTTTGGTATGGGATC[C/T]TGTTATGCACAGAAC | 55833 |
rs117855312 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929025 | TGGTTTCCTGGGGCT[C/T]CAAGGCGTCTTGTTC | 55833 |
rs117879906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933081 | TTTTCCTACACCTTG[C/T]TCTAATAACATCGTT | 55833 |
rs117911699 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001878 | ATTATAAGCTTTACA[A/G]GTCAAACACAAGAAA | 55833 |
rs117918420 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010818 | ATCCACTCACTGCAC[A/C]GTAAGTATTATTATA | 55833 |
rs117980523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984274 | TATCATCTAAGAAAT[C/T]TGCAGGATGATATTC | 55833 |
rs117989099 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983896 | CAAGAAACTTTACCT[A/G]GAATAATACTGAATC | 55833 |
rs117992497 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020398 | AGTGCGATCTCGGCT[C/T]ACTGCAACCTCCACC | 55833 |
rs118085978 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012400 | GCCAGGCATGGTGGC[A/G]CATGCCTATAATCCC | 55833 |
rs118115128 | snp | A/G | 0.0865458 | 0.189163 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935451 | TTTCGTATTTTAGTA[A/G]AGACAGAGTTTCACC | 55833 |
rs118156505 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976589 | TTCTGCGGTGTGGAA[A/G]ATGTTCTAAAATTGA | 55833 |
rs118177644 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33954885 | GTTCAAAACTGCCTT[C/T]ATTTCTAAGGTATCA | 55833 |
rs118184940 | snp | A/G | 0.104859 | 0.203554 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948965 | AGGTCAGCAGATTGA[A/G]ACCATTCTGGCTACC | 55833 |
rs137921582 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985173 | GGTTGTGGTGGCTGT[A/G]GCAATTTCTATTTTT | 55833 |
rs137976359 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942042 | ACTTAGGCTGCGTGC[A/C/G]GTGGCTCACGCCTGT | 55833 |
rs138049914 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980646 | TTCTGCATAAAGCAC[A/G]TTCAAAACAAAGTTA | 55833 |
rs138063138 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023377 | GATTTACAGAAAAAT[A/G]ACTTAATCTTTATAG | 55833 |
rs138125624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936660 | AAAAACAAAACAAAA[C/G]AAAACAAATAAATAA | 55833 |
rs138134520 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045969 | CTGCTTCTAAAATCT[A/G]TCAGAGATCTACTAA | 55833 |
rs138140692 | snp | A/G | 0.000209915 | 0.0102427 | missense | UBAP2 | GRCh38.p7 | 9:33922584 | AGCTGGGCTGGCTGC[A/G]CTGACCCGAGCCACT | 55833 |
rs138148861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931861 | CGCCCAACACCTCCT[A/G]TTGTCCAGGAGCATG | 55833 |
rs138157872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932102 | TCTAGGGCTACTCTT[C/T]GGCATATGAGGAAAA | 55833 |
rs138159192 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984452 | AGGACAGCTTGAGGC[C/G]AGGAGTTCCAGACCA | 55833 |
rs138160278 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031790 | ACCCTGTCCCAAACC[-/A]AAAAAAAAAAAAAGA | 55833 |
rs138170504 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049407 | AGAGCCGAGGGAAGG[C/T]CGGGACGGAAAGCGG | 55833 |
rs138173455 | in-del | -/CTAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008639 | GCGTAAGATATATAC[-/CTAT]TAACACTTTACAGAA | 55833 |
rs138241999 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003880 | ACATGCCACAATGCC[C/T]GGCTAATTTTTGTAT | 55833 |
rs138274627 | snp | A/G | 0.000344406 | 0.0131181 | missense | UBAP2 | GRCh38.p7 | 9:33922713 | GCGGAAGGTGGTGGT[A/G]CAGCAGCTGTGAGTG | 55833 |
rs138281279 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012820 | TTCCCATTGCAACTT[G/T]TCCGTAAATCTCACA | 55833 |
rs138281383 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981316 | GATATATATATATAT[-/AT]CTAGAAATACAAATA | 55833 |
rs138322900 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949981 | GAAAGCCTATGACTA[C/G]AAAAGACAATGGAAG | 55833 |
rs138345404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999028 | TATAACCTGTTCCCA[C/T]AGGAAAAATAAGCAT | 55833 |
rs138426198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968631 | ACTGAAATAATCATA[C/T]GGATTTTTCTCCTTA | 55833 |
rs138433229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957490 | ATTTTCTAGAATTTT[A/C]AATGAAATCATAAAA | 55833 |
rs138447237 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984869 | AATCCCAACTACTGA[A/G]GTGGCTGAAACAGGA | 55833 |
rs138534224 | snp | A/G | 5.01349e-05 | 0.00500649 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927958 | GAGAAGGTGGCTGAG[A/G]ACTGGTGGGAAGAGG | 55833 |
rs138541024 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048726 | GGGCAGTCTGCAGGC[-/G]GGTGGGGTTTCAGAC | 55833 |
rs138591305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937247 | AAAAGTCTGACAAAG[G/T]TTCAATTTAACTGCG | 55833 |
rs138605173 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016370 | CAGCGGCGGCAGCGG[C/T]GGTGGTGGTGGTGGT | 55833 |
rs138680124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942236 | AGAATCACTTGAACT[C/T]GGGAGGCAGAGGTTG | 55833 |
rs138694988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024017 | CCATTGCACTCCAGT[A/C]CGGGTGACAGAGCAA | 55833 |
rs138773817 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976158 | TTCAGCTAATTAGCT[C/T]TAAGAAGAAAACTTT | 55833 |
rs138777787 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028243 | GACATCAAAATTTAT[C/T]TGATATCGTCACAAT | 55833 |
rs138813398 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976263 | TAAAACCTTGAACTG[-/A]AAAAAAAAATGCAGT | 55833 |
rs138825543 | in-del | -/ATTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027170 | ATACCTGCAGAAGAC[-/ATTA]AAAGCTCAGATTAAG | 55833 |
rs138880045 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013641 | CAGCACTCTGGGAGG[C/T]CAAGGTGGGCGGATC | 55833 |
rs138894858 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967584 | AACAGTCATACATAC[G/T]TATCTGAAATAATGT | 55833 |
rs138911165 | snp | A/G | 0.000270039 | 0.0116167 | missense | UBAP2 | GRCh38.p7 | 9:33922793 | CCAGGGGCCGCTCCC[A/G]AGGCCAGGGGCCCAG | 55833 |
rs138921797 | snp | A/C/T | 4.95408e-05 | 0.00497678 | utr-variant-5-prime, synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33998835 | CTTATCAAAGATCAC[A/C/T]TGAGCGAGACGCATC | 55833 |
rs138922623 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989769 | TCACTTACCTCTCTA[C/T]TAGGCCTTAAATCTA | 55833 |
rs138975086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036136 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 55833 |
rs138994677 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989204 | ATGCATGTATCTTTC[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs139008872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956739 | AAACCAGGGCTCAAC[C/T]GCAGACTCACTTCTC | 55833 |
rs139014566 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966056 | TCCATCTCAAAAAAA[-/A]TAAAAAATCAGGGAG | 55833 |
rs139029922 | snp | C/G/T | 0.000390161 | 0.0139618 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953508 | ATGAGGAACCAGTCA[C/G/T]AAGCAAATCTTACCA | 55833 |
rs139036018 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006896 | TTGACAGTGACTACT[C/G]AACATATTATTTACT | 55833 |
rs139046885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934167 | AACATCTGCAGTCCA[A/G]CTGTCCAACACCTAC | 55833 |
rs139075074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046978 | AAGGCAACTCCATGT[A/G]ACTACTGCTGATCCA | 55833 |
rs139087111 | snp | C/T | 4.94499e-05 | 0.00497217 | missense | UBAP2 | GRCh38.p7 | 9:33948428 | TGAGGTCCCAAGAAG[C/T]AGTAGTTGTAGGGTG | 55833 |
rs139137712 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931380 | GAGACGATTCTGGCT[A/G]TGGCAGGCTGGAATA | 55833 |
rs139154948 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924645 | CTAGGAAAGCTGACT[A/G]AACAGAGCAGACCTG | 55833 |
rs139155369 | snp | C/T | 0.188 | 0.24219 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976968 | AGTGAGCCGAGATGG[C/T]GCCACTGCACTCCAG | 55833 |
rs139156856 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014439 | TTGGAGACCAGGCTG[C/G]GCAACATGGTGAAAC | 55833 |
rs139175743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013359 | ATTCAAGACCAGCCT[C/G]ACCAACATGGTGAAA | 55833 |
rs139216466 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963671 | AAAATGAAAGATATT[A/G]CAAGCAATTTATAAG | 55833 |
rs139247120 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050206 | TAAACAAGCTCTCAA[G/T]GTCTACTTACTGGCC | 55833 |
rs139328070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928702 | TAGCAACAGGGTCCT[A/G]TGAAGAACTTCAAGC | 55833 |
rs139367591 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939418 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGATCTCA | 55833 |
rs139373837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034126 | TCAACATTTGGCACT[C/G]AAATGTCACAAATTC | 55833 |
rs139405776 | in-del | -/TA | 0.0573587 | 0.15934 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982541 | ATAGTTTAAATGGAC[-/TA]TGTTTTTGATTGTTT | 55833 |
rs139434718 | in-del | -/G | 0.108186 | 0.205885 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986753 | TTCCCTCTTACTCTA[-/G]AGCTTACCTCTACCC | 55833 |
rs139439472 | in-del | -/TTC | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950065 | AAAATAACATTTCTT[-/TTC]TTTTCTTTTTTCTTT | 55833 |
rs139480314 | snp | C/T | 0.000732447 | 0.0191229 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927985 | GAGGCGCTCTCCACA[C/T]TGGCATGCTGGCAAA | 55833 |
rs139557726 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049949 | TTTTAAAGTATTTTC[C/T]ATTTACTGGCCTGTT | 55833 |
rs139576686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954577 | CTAACTGACATTCTC[A/G]CCATGCCAATAAGAC | 55833 |
rs139577156 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970717 | ACTACAGGCATGAAC[C/G]ACTGCACCTGGCCTT | 55833 |
rs139578711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036765 | AATGTAAACTTAGCA[A/T]TCACAGAAATAACAG | 55833 |
rs139592812 | in-del | -/C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993897 | TCAGCTTTGCTTTCT[-/C/T]TTTTTTTTTTTTTTT | 55833 |
rs139649082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043924 | CCTGAGGTCAGGAGT[C/T]CAAAACCAGCATGGC | 55833 |
rs139650727 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033598 | TTTTTTTTCTCCTGA[C/G]ACAGGGTCTGACTCT | 55833 |
rs139662606 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038103 | ACGGGGAGTTCAAGG[A/C]TGCAATGAGCTAGGA | 55833 |
rs139743293 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029786 | TGAGATCAGGAGTTC[C/G]AGATCAGCCTGGCCA | 55833 |
rs139804703 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957559 | TAATTATTTTGGGAT[A/G]TATGCACACTGTTTT | 55833 |
rs139816798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001255 | ATTTAGAAAGAATAT[A/G]TAAGTAGGATTGCAA | 55833 |
rs139845107 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020394 | GAATAGTGCGATCTC[A/G]GCTCACTGCAACCTC | 55833 |
rs139880777 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929134 | AACTAGGTTCTCACT[A/C]AGGAGGCAGACTCCC | 55833 |
rs139891703 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015397 | GATCTTGGCTCACTG[C/G]AACCTCTGCCTCCCG | 55833 |
rs139901839 | snp | A/G | 0.000463553 | 0.0152172 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953312 | AGAACAGGAGTTGAC[A/G]GCAGTGGAGCTGCCA | 55833 |
rs139962175 | in-del | -/CTCCATTTA | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046061 | AATAACAACTAAGAG[-/CTCCATTTA]CTCCATTTACTCAAA | 55833 |
rs139975984 | in-del | -/TG | 0.00993419 | 0.0697739 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993572 | GGCTACTCGGCAGGC[-/TG]GAGGATGGCATAAGC | 55833 |
rs140050352 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999455 | CTTTGTGTCAAAAAA[C/G]CTCTGTTGTCAGGTC | 55833 |
rs140103338 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992303 | TGAGGCGGAAGAATC[A/G]CTTGAACCCGGGAGG | 55833 |
rs140136942 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981815 | AAGGAAGGGTGGAAG[C/G]GGGGAAGCGGGGAAG | 55833 |
rs140149993 | snp | C/T | 0.000148592 | 0.00861823 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956160 | AGCTGTATGGAAAGT[C/T]GAAAAATTTAATCTT | 55833 |
rs140158168 | snp | A/G/T | 0.000709153 | 0.0188177 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33988992 | TCTGCCACGATTGCC[A/G/T]CCTCTTCCTTTCCGG | 55833 |
rs140183656 | in-del | -/GGAGGAGAAGA | 0.188631 | 0.242351 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939911 | GGAGGAGGAGGATGG[-/GGAGGAGAAGA]AGAGGAGAAGGAAGA | 55833 |
rs140194238 | snp | A/G | 0.00148148 | 0.0271762 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923286 | CCCCTGGGTCAGGTC[A/G]TCATAACCTAGCGTG | 55833 |
rs140226006 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964661 | ACTAAGATTACGCCT[A/G]TGAATACCAACTACA | 55833 |
rs140244132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978724 | GGGGGAGCGTGCAAT[A/G]AGCCGAGATTGTGCC | 55833 |
rs140260131 | snp | A/C | 0.000329451 | 0.0128303 | missense | UBAP2 | GRCh38.p7 | 9:33923985 | GAGTCCCCACGGCCA[A/C]ACTTTGTGACATCAC | 55833 |
rs140305959 | in-del | -/AAAAAAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934799 | CCTAGACAAAAGAAA[-/AAAAAAC]CCTGCCACTACCACT | 55833 |
rs140323302 | in-del | -/ATT | 0.0479149 | 0.147179 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045432 | GGCTGGATGAAGTCC[-/ATT]AATGGCACATGGCTC | 55833 |
rs140352022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33952121 | CAAACGATTTGACTC[A/G]GGAGAAAATTCTGTT | 55833 |
rs140479290 | snp | C/G/T | 0.000252965 | 0.0112437 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922591 | CTGGCTGCGCTGACC[C/G/T]GAGCCACTCTGAGGA | 55833 |
rs140483196 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004985 | TTGAAAACAACAGTC[A/G]GGCATGGTAGCTCAG | 55833 |
rs140492275 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946442 | CATTTTGGCATAGAG[A/G]TCCAACTTCATTTTT | 55833 |
rs140519988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931448 | GCAGCTCCCCATGAG[A/T]GCAGGAGCACTGGGC | 55833 |
rs140541348 | in-del | -/T | 0.444799 | 0.156695 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999907 | ATGTATGTATGTATG[-/T]TTATTTTGAGATGGA | 55833 |
rs140566412 | in-del | -/A | 0.108048 | 0.20579 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004785 | CGAGATTCTGTCTCC[-/A]AAAAAAAAAATAGGG | 55833 |
rs140605759 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972650 | GAAGCAACAAAAAGT[-/A]AAAAAAACACCCAGA | 55833 |
rs140606057 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010722 | GGAGTACAGGCGGCG[A/G]CTTGGGGTGGTAGAT | 55833 |
rs140609988 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039947 | GCGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA | 55833 |
rs140653385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925597 | GTTTGGGCCTTTGGC[C/T]GGCAGATTAAAGGGC | 55833 |
rs140656279 | in-del | -/AAAAC | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942424 | GAATGTGAAAAAACT[-/AAAAC]AACAACAACAACAAA | 55833 |
rs140660824 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006959 | TGAGTACCTGAACAA[G/T]GTAGACAGAGTACAA | 55833 |
rs140689341 | in-del | -/A | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932267 | AAAGAAGGCACGAGG[-/A]AAAGATCAAACAGCA | 55833 |
rs140701920 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961427 | TACTCTTGCTCATAT[A/C]AAGTCTGCTGCTTTA | 55833 |
rs140761321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030701 | GGAGGCCCGGGCGCA[C/T]GGATCACAAGGTCAG | 55833 |
rs140779523 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044531 | GGCACCACAGCACTC[C/T]AGCCTGGGCGACAGA | 55833 |
rs140786469 | in-del | -/AAATAC | 0.0872718 | 0.189788 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954724 | AATTCACTGAATCAT[-/AAATAC]AATAGAGAATATGTG | 55833 |
rs140788101 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010045 | CTCCTGACCTCAGGT[A/G]ATCTACCTGCCTTGG | 55833 |
rs140796836 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960648 | AGCCAGGCATGGTGG[C/T]GCACATCTGTAATCC | 55833 |
rs140818153 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984629 | GTTGCAGTAAGTTAT[C/G]ATCATGCCACTGCAC | 55833 |
rs140818254 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924909 | TGTTTGCAATTTTTT[A/T]AAGCTCATCAGCTAT | 55833 |
rs140901861 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982578 | CTGTTCCTATTCACC[A/G]GTATATATACTGATG | 55833 |
rs140922028 | snp | A/G | 0.000938542 | 0.0216423 | missense | UBAP2 | GRCh38.p7 | 9:33941788 | CTTGTCAGACTGCAG[A/G]AGGTAATGACGGAAG | 55833 |
rs140928248 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936546 | TGATCCACCCACCTC[A/G]GCCTCCCAAAATGTT | 55833 |
rs140970884 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995350 | TGGCAGAGTGAGGCT[C/G]TCTCAAAAAAATAAA | 55833 |
rs140981035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938257 | CCTCAGTCTCCCAAA[C/T]TGCCAGGACCACAGG | 55833 |
rs141035311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017572 | TAGCCCAATTTAAAA[C/T]GTGTCAAGAAACAGG | 55833 |
rs141067561 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940421 | AAACCTTGGACATAC[A/T]GAGTTGTTGAGCTGA | 55833 |
rs141087033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027595 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55833 |
rs141092531 | in-del | -/AAC | 0.187685 | 0.242109 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942426 | ATGTGAAAAAACTAA[-/AAC]AACAACAACAACAAA | 55833 |
rs141117652 | in-del | -/AATAAT | 0.445855 | 0.155373 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991304 | AGACTCTGTATCAAA[-/AATAAT]AATAATAATAACGTA | 55833 |
rs141121044 | snp | A/G | 5.16898e-05 | 0.00508353 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927063 | GCACCCCCTGAGGTA[A/G]GTTTGGGGGTGCTTT | 55833 |
rs141125550 | snp | A/G | 0.00603228 | 0.0545871 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944598 | GTTGTCGCTGGCTCA[A/G]CTGGCTAAGAACTGG | 55833 |
rs141150500 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981780 | AGGTAGGTAGGAAGG[A/T]AGGAAGGAAGGAAGG | 55833 |
rs141204564 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987181 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 55833 |
rs141210006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933154 | TCCATCATTCTCATT[C/G]CACCTCAGTGACATG | 55833 |
rs141241582 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034803 | GCTTCAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 55833 |
rs141273068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952856 | TTTTCTGGACTAAGA[C/T]CTACTGTAGAATTTT | 55833 |
rs141274332 | in-del | -/GGA | 0.448066 | 0.152544 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992656 | GACAACTTATCGGGC[-/GGA]GGGGGGGGGGCACAA | 55833 |
rs141342981 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045239 | TAGTCCCAGGTACTC[A/G]GGAGGCTGAGGCAGG | 55833 |
rs141355238 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013831 | GCAATGAGCTGAGAA[C/T]GCGCCACTGCACTCC | 55833 |
rs141358835 | in-del | -/GGG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016245 | GAGGAAGGGGAGGAA[-/GGG]GAGGAGGAGGAGGAA | 55833 |
rs141380123 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921305 | GGTATACCTGTTCAT[A/G]CTCTCCCTTAAGGCC | 55833 |
rs141384768 | in-del | -/ACACACACAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019689 | TATGTACATTTTACT[-/ACACACACAC]ACACACACACACACA | 55833 |
rs141388407 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006709 | ATAACGTAAAGAAAA[C/T]GTGGGCCTAGCACTT | 55833 |
rs141428929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047379 | CCACAGGTGAGTGTA[C/T]TGAAGGAAACTATCA | 55833 |
rs141478082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045918 | CCCTCTCTTTGCCTT[C/T]CTTCAGGTTGTATCT | 55833 |
rs141497376 | snp | A/G | 0.000148467 | 0.00861461 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927916 | GCGCCTGAGGATGCG[A/G]AACTTGAGACGGAGG | 55833 |
rs141541169 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033332 | GGATAGAACCGGAGA[G/T]CATTATGTTAAGTGA | 55833 |
rs141557492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998435 | GGTAATTCAGTTCAT[C/T]TCTAACATTAAACAC | 55833 |
rs141611236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022335 | TCCAAGCTGGGCAAG[A/G]TGGCATGCACCTGTA | 55833 |
rs141644899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035921 | TTGAGTGGGGGAAAT[C/T]GCTTGAGCCCAGGTA | 55833 |
rs141648325 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018549 | AGAGTCTCAAAGAGA[C/T]GCTTGTACTTCCATG | 55833 |
rs141657290 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020552 | GCTGGTCTCAAACTC[A/G]TGGCCTCAGGTGATC | 55833 |
rs141736382 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974273 | AGCACTTTGGAACAC[C/T]GAGGCAGTTGGACTG | 55833 |
rs141741440 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976386 | TCCCTTCAGGGTAAA[C/G/T]GCGATGGGGAACCCA | 55833 |
rs141751803 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036983 | CACCACACCCAGCTA[-/T]TTTTTTTTTTTTTTT | 55833 |
rs141787516 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970081 | ACCACAGGCATATGA[C/T]ACTATGCCCGGCTAA | 55833 |
rs141862182 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979981 | GGGAGGCTAAGGCAG[A/G]AGAATTGCTTGAACC | 55833 |
rs141873953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957495 | CTAGAATTTTAAATG[A/C]AATCATAAAAGTATC | 55833 |
rs141897349 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007814 | CGGCTAATTTTTTTT[C/T]CCATTTATAATAGAG | 55833 |
rs141908597 | in-del | -/A/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992390 | CAAAACTCCATCTCA[-/A/AA]AAAAAAAAAAAAAAA | 55833 |
rs141917867 | snp | G/T | 3.61526e-05 | 0.00425147 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922765 | GATGTGTAGGAATGG[G/T]GGGGGTGCATAGCCA | 55833 |
rs141955869 | in-del | -/AAAAGGAAAT | 0.467439 | 0.123371 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005648 | AATTTTTTTCCTGTA[-/AAAAGGAAAT]AAAAGGAAAGAGAAA | 55833 |
rs141988878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953212 | GTAATTATAAAGCAT[A/G]TATCATATTCTAGAA | 55833 |
rs142027964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002000 | ACAGGGTTTCACTCT[C/G]TGTTGGAATGCAGTG | 55833 |
rs142032256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949325 | CACATTATTTTCCTA[C/G]TCTGTGAACCACAGT | 55833 |
rs142047415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999936 | AGTCACACTCTGTCG[C/T]CCAGGCTGGAGTATT | 55833 |
rs142074005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997142 | CAAAACACACTCCTA[C/G]ACATATTTTCTCAAG | 55833 |
rs142124694 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046948 | AGGTGTTATTGTTGT[A/T]CCAATATAGTTCTAA | 55833 |
rs142128588 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923936 | TTGGCTCTGCTGTGG[C/T]TGAGCTGGTGTGGTA | 55833 |
rs142138194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953958 | CTTACCAAGGCTGGA[A/G]TGCAGTGGTGTGACC | 55833 |
rs142153527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952530 | TTAGGGGGAAAAAAA[A/G]GCAAAAAATGTAAGC | 55833 |
rs142177201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003847 | GTCTCAGCCTCTTGA[A/G]TAGCTGGGATTACAG | 55833 |
rs142184006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005214 | GTTGCAGTGAGCTGA[C/G]ATCTCACCACTGTAC | 55833 |
rs142202194 | in-del | -/ATCAGCATTTTATTAAATGCT | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978165 | GTAACTGATTTGAGA[-/ATCAGCATTTTATTAAATGCT]ATGTGGAACAAGGAC | 55833 |
rs142252402 | snp | C/T | 0.0158583 | 0.0877198 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027251 | TTTGGGAGGCTGAGG[C/T]GGGAGGATTACTTGA | 55833 |
rs142253674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957266 | TCACATTCTAACACA[C/T]CCAATAAACCGCAAA | 55833 |
rs142268445 | snp | C/T | 0.000115345 | 0.00759337 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33973228 | CCTCTCCCTCTGCCA[C/T]GTCCAAATCCTTTAA | 55833 |
rs142290252 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037529 | AAACTTAGGGTTGGC[A/G]TAGCAGTCATGGAAT | 55833 |
rs142399229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979114 | GTGATGTGCACCTGC[A/G]GTCCTATCTACTCAG | 55833 |
rs142423499 | in-del | -/C | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020064 | CTAGGGAGGCTGAAG[-/C]CAGGATAATTGCTTG | 55833 |
rs142461082 | snp | A/T | 0.15698 | 0.23205 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977046 | GTTTTTTATTTATTT[A/T]TTTTTTTTTTGAGAC | 55833 |
rs142469786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973348 | TATCATTATTCCTAG[C/T]AGCACCAACATTCCA | 55833 |
rs142501796 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948491 | TGGTAAACTGGCCCA[A/G]ACTCGGAGCTTTCAA | 55833 |
rs142506888 | snp | G/T | 6.59598e-05 | 0.00574243 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33996229 | AATACTTACTGTGTC[G/T]GAATTCCCTTCCAGC | 55833 |
rs142519059 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930770 | GCATGGTGGTATGCG[C/G]CTGTAACCCCAGCTA | 55833 |
rs142537937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932430 | CGAACCAGATCATGC[C/T]ATCAAGACATTTCAG | 55833 |
rs142595753 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027323 | CTACCCTACTAAAAA[-/T]ACAAAAAATAAGCCA | 55833 |
rs142636146 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960556 | TGAGGCGGGTGTATC[A/T]CCTGAGGTCAGGAGT | 55833 |
rs142686968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949736 | ATGCACGCGCACACA[C/T]GCACAAGATCAAATA | 55833 |
rs142691376 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030885 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA | 55833 |
rs142697900 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995356 | AGTGAGGCTGTCTCA[A/C]AAAAATAAATAAATA | 55833 |
rs142705828 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936712 | TAGATCTCAGAAACA[C/T]TAAAAGGACAGGAAA | 55833 |
rs142711897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029079 | TATGATCATGTCACC[A/G]CACTCCAGACTGGGC | 55833 |
rs142753545 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983617 | TAAAATTTAGGGGTC[A/G]ATAAAGTCATTTTAT | 55833 |
rs142784846 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951420 | GGCATGATCACGGCT[C/T]GCTGCAACCTCCACC | 55833 |
rs142830502 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000858 | CCAACCTATGCCTGC[A/T]GAGACCTCAGTTTAA | 55833 |
rs142945568 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999043 | TAGGAAAAATAAGCA[C/T]CAAATTAAGTAACAT | 55833 |
rs142983479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040898 | AGCTGACAAGCCTGA[A/G]AACAACTGTGCAACA | 55833 |
rs142985271 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930198 | GATGCCATGGTGTAA[C/T]AGGATATTTCATTCA | 55833 |
rs142986969 | snp | C/T | 0.000313064 | 0.0125074 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017117 | TTTTCCCGAGCACCT[C/T]GACAATGGTCACTGC | 55833 |
rs142993222 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992106 | AACATACAAAAATTA[C/G]CAGCCGGGTGCAGTG | 55833 |
rs143030332 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008615 | ACAGAGATTGTGTCT[C/G]GACTGCAAAGCGTAA | 55833 |
rs143050750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956622 | GTATAAGCCATGGCG[C/T]CCGGCTGCAAGTGAA | 55833 |
rs143105522 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998131 | TGAAATGGCAATTCA[A/G]GCCAGTAATCCTGTA | 55833 |
rs143111805 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988789 | TCTGCATTGAGGAAA[C/T]GAATTTATGAGCATA | 55833 |
rs143116456 | in-del | -/C | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018387 | GTACAAAAACTAGAA[-/C]CCTTGTGCACTGCTG | 55833 |
rs143120629 | snp | A/G | 0.0046339 | 0.0479111 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960792 | TTTCAAAAAAAAAAA[A/G]AAAGAAAGGTCTCAT | 55833 |
rs143151663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034646 | TTGGGAGGCACAGGC[A/G]GGCGGATCAGGAGGT | 55833 |
rs143176847 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976008 | ATCGCTTGAGGCCAG[G/T]AGTTCAAAACCAGCC | 55833 |
rs143221367 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028399 | ATTTATTTATTTTGA[G/T]ATGGAGTTTCACTGT | 55833 |
rs143290998 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964166 | GGGTCCCTCATATCA[A/G]GAATAGATTTGTGGT | 55833 |
rs143366803 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962096 | ATTGTAAGAGAAAGC[G/T]TGATGGCGAAGATAA | 55833 |
rs143401700 | snp | G/T | 0.000807521 | 0.0200776 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953416 | AAGTTTCAAAGGAGT[G/T]GGCTTCTGAGGCTTG | 55833 |
rs143411935 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937737 | ACATGATGAAACCCC[A/G]TCTCTATTTAAAAAA | 55833 |
rs143412843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970784 | AATTCATTGTGTTAA[A/G]TTATGTTTCTGTTTT | 55833 |
rs143424765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952865 | CTAAGATCTACTGTA[G/T]AATTTTTTGATGTTT | 55833 |
rs143442837 | snp | C/T | 0.00011536 | 0.00759387 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:34017071 | CACTTGTTTCTGTGG[C/T]TGCGTTGATTGTGCT | 55833 |
rs143452486 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985941 | TAGGAGGATTGTTTG[A/T]GCCCAGGAGGTGGAG | 55833 |
rs143466465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002843 | ACAGGCGCACAACAC[A/G]ACACCTGGTTAATGT | 55833 |
rs143528434 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030396 | GGAGGTTGCAGTGAG[A/C]CGAGATCGCGCCACT | 55833 |
rs143579034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993013 | ACAACTTACTAAAAA[C/G]AGTTAAGTACATTAA | 55833 |
rs143581752 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046605 | GCCGAGATCAGGCCA[C/G]TGCACTCCAGCCTGG | 55833 |
rs143612468 | in-del | -/TTAT/TTATTTATTTAT | 0.490343 | 0.0688145 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028361 | GCTGTAAACCCTGTC[-/TTAT/TTATTTATTTAT]TTATTTATTTATTTA | 55833 |
rs143621315 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987959 | ATATTGGCATTAATA[A/G]CTCTACATAATACAG | 55833 |
rs143662986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951100 | ACAGAACAACCTCCT[A/G]GGCTCAAGTGATCCT | 55833 |
rs143694215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923637 | TCTAAACACAGCAGG[A/G]GAAAAGTGACCTTGT | 55833 |
rs143704831 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027175 | CTGCAGAAGACAAAG[C/T]TCAGATTAAGAATCT | 55833 |
rs143721247 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935584 | AGCATCTTTAAAATG[C/T]ATACTGTATGCTGCA | 55833 |
rs143744129 | snp | C/G | 0.0146672 | 0.084371 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049597 | GCTAGCAGCGAGAGC[C/G]TCGGCAAGGCGGAAG | 55833 |
rs143780579 | snp | C/T | 0.000421622 | 0.0145132 | missense | UBAP2 | GRCh38.p7 | 9:33922868 | GCATGAAATCCCTGC[C/T]TGTCAAAAGTCTACA | 55833 |
rs143790607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007306 | TGAAACCAGCCCTGT[A/G]GGTAACTTGGTGAGA | 55833 |
rs143810736 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020149 | AGGGAGACTCCATTA[-/T]TTAAAAAAAAAAAAA | 55833 |
rs143815917 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969512 | TATGATCACACTACT[A/G]CACTCCAGCCTGGAC | 55833 |
rs143872140 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045985 | TCAGAGATCTACTAA[C/G]TTACCAGTCAACACC | 55833 |
rs143955238 | snp | A/G | 0 | 0 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050305 | TTCCTCTGTAATAAC[A/G]CTTCACCGGCTTGTG | 55833 |
rs143984490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972099 | AAAATAAGGCATAAA[C/T]AGGCAACAGGTATTT | 55833 |
rs143989390 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940827 | ACACTGAATGCTCAC[-/AT]ATTAATTTTTAGCAT | 55833 |
rs144003966 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965036 | TCACGGATTTGTTTG[C/T]TATCCATTTATCATG | 55833 |
rs144009089 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047245 | TCAACTAGCCATAAG[C/T]AGGAAAATCAGGAGT | 55833 |
rs144024533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928910 | CGCAGACTAACTCTC[C/T]GCCGCCATCCCATGC | 55833 |
rs144044736 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924703 | CCTGAAAGGTTTAAG[G/T]GGGGACAGGGGGCAG | 55833 |
rs144046242 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963889 | GCTATGTATATGCTG[A/C]GTTACTGCCCAAGGA | 55833 |
rs144068691 | snp | A/G | 0.232651 | 0.249397 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031554 | TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 55833 |
rs144078066 | snp | A/C | 3.29478e-05 | 0.00405867 | missense | UBAP2 | GRCh38.p7 | 9:33944467 | CGTGCTGGGAAGCTG[A/C]AAAAGCTTGTTCACA | 55833 |
rs144145639 | snp | C/T | 8.49553e-05 | 0.00651693 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927974 | ACTGGTGGGAAGAGG[C/T]GCTCTCCACACTGGC | 55833 |
rs144154116 | in-del | -/TTTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028369 | CCCTGTCTTATTTAT[-/TTTA]TTATTTATTTATTTA | 55833 |
rs144209629 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935675 | TTAAGACATTTCTAA[-/T]TAACACCACAGCCAA | 55833 |
rs144218210 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955039 | GAATGTGGTTATCCC[A/G]TAAGTTCCTTCCTTT | 55833 |
rs144231292 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030304 | CAAAAACAAAATTAG[C/T]CAGGCGTGGTGGCGG | 55833 |
rs144315178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950981 | TTTTGTTTTAGAGAC[C/T]TGGGAAATATCATCA | 55833 |
rs144324389 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032443 | CCACTAGTTACTCTG[C/T]CCCAAGGCTTCACAG | 55833 |
rs144453716 | in-del | -/ATT | 0.345037 | 0.231231 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011995 | CCACCAAAGATAAAC[-/ATT]ATTAACAGTCTACTA | 55833 |
rs144480091 | snp | A/G | 1.65866e-05 | 0.00287976 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932578 | GTGTGTGACGTGCTC[A/G]AGGAGAGGGCTGCAT | 55833 |
rs144486522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937281 | GGGGTGTAAATAAGT[A/C]AAATTATCTAGCATG | 55833 |
rs144487666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024283 | GGAGGAAGAGGTTGC[A/G]GTGAGCCAAAATTGC | 55833 |
rs144489543 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050165 | GAGTAGCTGCACGCC[C/T]GTGTTAACAAGCTCT | 55833 |
rs144542195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043342 | CAGCTAATTTTTGTA[C/T]TTTTAGTAAAGACAG | 55833 |
rs144569253 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924598 | GGGCTGAACCAACTT[C/T]GCTGGCTTTTCTGTG | 55833 |
rs144638331 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037841 | ATGTAAATACAGAAA[-/A]CCCCGACTGGATGGG | 55833 |
rs144665095 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000494 | GAAATTAGGTGAGGA[A/G]TATACAGGAACAATC | 55833 |
rs144685100 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042422 | GGTGGAGGTTGCAGT[A/G]AGCTGAGATCGGGCC | 55833 |
rs144703983 | snp | C/T | 0.00300018 | 0.0386146 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927813 | TGAGGTCACCAAGGG[C/T]GCGGCCCTGCTACTG | 55833 |
rs144728975 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952517 | TATTTTACGGTCTTA[-/G]GGGGGAAAAAAAAGC | 55833 |
rs144736695 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937093 | GAACAATCCAACACA[A/C]ACTCTTTCTAAAAAA | 55833 |
rs144742733 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023992 | GAGTCTGCAGGGAGC[C/T]GAGATGGCGCCATTG | 55833 |
rs144811630 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934898 | GCAGCCCAACAATAC[C/G]AGCAAATGTCAAACC | 55833 |
rs144832217 | snp | A/G | 0.00370086 | 0.0428571 | missense | UBAP2 | GRCh38.p7 | 9:33943507 | GAGAGAGAAGGTTCT[A/G]ACCCAAATTCCAGAG | 55833 |
rs144897960 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972519 | TGCTGCCTGAAGTTA[G/T]AGAGAGACAAAGGGC | 55833 |
rs144907734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940423 | ACCTTGGACATACAG[A/G]GTTGTTGAGCTGAAA | 55833 |
rs144926944 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938677 | GATGGGTGCCTGTAA[C/T]CACAGCTACTAGGGA | 55833 |
rs144938708 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025216 | TGTAGTAAATAGGAA[C/T]GCTTCTACAACAAGT | 55833 |
rs144945277 | in-del | -/G | 0.0437281 | 0.141251 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959544 | CAGTCAAACAGAAAA[-/G]AGGTATAAAATTTTA | 55833 |
rs144982320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33952233 | GACCTTTCTAACTTC[C/T]CCTTGCCAGCTCAGA | 55833 |
rs144986572 | snp | A/G | 0.000131774 | 0.00811601 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923401 | GTAGCCGTGCTGGCC[A/G]TAACCACTGGCCTGC | 55833 |
rs145009226 | in-del | -/AGG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016289 | GGAGGAAGAGGAGGA[-/AGG]GGAGGAAGAGGAGGA | 55833 |
rs145016608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936584 | CAGGTGTGAGCCACC[A/G]TGTGAGCTGACATTG | 55833 |
rs145078840 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046669 | AAAAAAAAAAAAAAA[-/AAAA]GAAGGCTTCACTTCA | 55833 |
rs145120323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034549 | AAACACTACACTAAT[A/G]AGAAATACCCCACAT | 55833 |
rs145152622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006766 | CAAGTATAAAAGGTA[C/T]AAATTGTGAACACCA | 55833 |
rs145188395 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001673 | CAATTTTCACAAAAT[G/T]AAAGTAGACTGTTAG | 55833 |
rs145247571 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026461 | GATACACAATTTATG[G/T]TAAAGAAGCAAGTCT | 55833 |
rs145305219 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004599 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 55833 |
rs145401841 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021208 | GGTCTGACAAGCATT[A/T]TTCTGTGTTAGCTGC | 55833 |
rs145468627 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044608 | GGTGGCTCACGCAAG[C/T]AATCCCAGCACTTTG | 55833 |
rs145482059 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929689 | AAAGACCTGACAAAA[A/C]AAGGAACCAAGAATA | 55833 |
rs145507881 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029766 | AGGCCAAGGCAGGTG[C/G]ATCATGAGATCAGGA | 55833 |
rs145546972 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978732 | GTGCAATGAGCCGAG[A/T]TTGTGCCACTGCACT | 55833 |
rs145578872 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983911 | AGAATAATACTGAAT[C/T]CCTGGGATTTTTTTA | 55833 |
rs145589963 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026094 | AAAACCATGTATATA[A/C]CCTAAACGAAAAGCA | 55833 |
rs145617836 | snp | C/T | 8.83119e-05 | 0.00664441 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948327 | ACACTCTGCCAAAGC[C/T]TGAAACGTCCTCAGT | 55833 |
rs145638776 | snp | A/G | 7.25637e-05 | 0.006023 | missense | UBAP2 | GRCh38.p7 | 9:33922701 | CCTGTGCATCCTGCG[A/G]AAGGTGGTGGTGCAG | 55833 |
rs145658062 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995233 | GTGGTGGCGCATGCC[C/T]GTAGTACTAGCTACT | 55833 |
rs145681842 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981898 | GAGAGAAGAGGTACA[C/G]TACAAAAAATAATGT | 55833 |
rs145740584 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBAP2 | GRCh38.p7 | 9:33941839 | ACTGCACTGGTCATT[A/G]ATAAAGATGTATTCA | 55833 |
rs145745810 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957376 | ATTCTTTACTCCCCC[A/C]CAATTTCCACCTGTC | 55833 |
rs145758424 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040089 | ACTTGAACCCAGGAG[G/T]CGGAGGTTGCGTTGA | 55833 |
rs145777023 | snp | A/G | 0.0130921 | 0.0798413 | | | GRCh38.p7 | 9:34030197 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 55833 |
rs145797044 | in-del | -/CGGG | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048416 | TCCCAAGACTAGCTA[-/CGGG]CGTGAAAGCGGAAAG | 55833 |
rs145878205 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044843 | TGCACTCCAACCTGG[G/T]TGACAGAGCGAGACT | 55833 |
rs145893207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002259 | ACACTTGGCTATTTT[A/C]CTCTTTTATCAAAAA | 55833 |
rs145903033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961646 | ACACTAAGAAATTAA[C/T]GACAACCCCAGAAAG | 55833 |
rs145961295 | snp | C/T | 1.65721e-05 | 0.0028785 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017148 | TCACTGAAGTCATCA[C/T]ATACAGTATATACAA | 55833 |
rs145967427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015291 | AATTGAGGAGGAGGG[A/G]GTATTTAACATTAAA | 55833 |
rs146013468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952607 | ATTCTGATAAACTTT[C/T]GCATTTAATTGGAAA | 55833 |
rs146015279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932693 | GATGAACAAGACGCA[C/T]GTGGGTCAGTGAGCT | 55833 |
rs146051282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037429 | AGAGAGCCACTGCGC[C/G]CAGCCCATATACTAC | 55833 |
rs146113668 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005260 | AGAGTGAAACTGTGT[C/T]TCAAGAAAAAAAAAA | 55833 |
rs146136674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999071 | CATAAAGGACCCATT[C/T]CTTTGACCAAACGAC | 55833 |
rs146206279 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970963 | ATGTGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 55833 |
rs146255018 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976699 | GTAAATTTTGTAAAG[A/C]ATATTTTCTTTCTTA | 55833 |
rs146325781 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951214 | AGCAAGATGAGGCCT[C/T]GCTATGTTGCCAGAC | 55833 |
rs146330267 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033556 | CACAATAGGGTAACT[A/G]TAGTCAATAACTTAA | 55833 |
rs146365437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036693 | TCAAGTGAACACCTA[C/T]AGAGTAGCATATACC | 55833 |
rs146413745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009885 | GGATCTCTGCTCATC[A/G]CAACTTCCGCCTCCT | 55833 |
rs146414724 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924732 | AGTGCCAGGTAGGCA[C/T]GGGAATAAGCAGGAC | 55833 |
rs146425331 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006587 | AGGCTGAGGTAGGAG[A/G]ATTATCTGAGTCCAG | 55833 |
rs146433815 | in-del | -/ATG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999905 | TATGTATGTATGTAT[-/ATG]GTTATTTTGAGATGG | 55833 |
rs146451477 | in-del | -/TT | 0.118839 | 0.212831 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012841 | AAATCTCACAATGTA[-/TT]TTTTTTTTTTTTAAA | 55833 |
rs146466765 | in-del | -/G | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026372 | AACAGAAAAACTAAT[-/G]TTTTTTTCAAACCAA | 55833 |
rs146475912 | in-del | -/CAA | 0.246485 | 0.249975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957900 | ACCGGTTCAACAAGT[-/CAA]CAAGAAGGGCCTAAG | 55833 |
rs146497777 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933628 | CCTGTTGTCTTTGGA[A/G]CTGGAACAGATGAAG | 55833 |
rs146537467 | snp | A/G | 0.000840911 | 0.0204878 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986843 | TCACCTCTAACTAGG[A/G]GGAAAAGAGCAGAAA | 55833 |
rs146548017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983632 | AATAAAGTCATTTTA[C/T]TCTTTCTTTTTGTTA | 55833 |
rs146549343 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033954 | TTGGCCAAGCTGTTC[C/T]TGAACTCCTGACCTC | 55833 |
rs146579366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926816 | CAGATCCTGCCTTCA[C/T]GGAGTCTAGATGGAA | 55833 |
rs146634288 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047370 | GAAGGGGCTCCACAG[G/T]TGAGTGTATTGAAGG | 55833 |
rs146654318 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964543 | ACACAGTTCTTCCAC[A/G]CTGTGTGGAAGCTGT | 55833 |
rs146665997 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961169 | TGCTTCAATATAGGT[C/G/T]ACATCCAAGCAATTC | 55833 |
rs146668598 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016260 | AGAGGAGGAGGAGGA[A/G]GAGGAGGAAGAGAAG | 55833 |
rs146709448 | in-del | -/A | 0.294576 | 0.245994 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951158 | ATTACAGTAGCTATG[-/A]TTACAGGGCATGTGC | 55833 |
rs146755345 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030310 | CAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT | 55833 |
rs146767784 | snp | A/G | 1.64795e-05 | 0.00287045 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996248 | TTCCCTTCCAGCAAT[A/G]TATTGATAGCTTTGT | 55833 |
rs146779433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946090 | AATTGGTGGAAAATG[C/G]TATTAAAAAATACAA | 55833 |
rs146790633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940164 | ATCGGATGCATGCAG[C/G]CAGATTTAATATGGG | 55833 |
rs146851274 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017722 | ATGAGGTCAGGAGAT[C/T]GAGACCATGCTGGCT | 55833 |
rs146878014 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010381 | GTGAGCCCAGATCGC[A/G]CCACTGCACTCCAGC | 55833 |
rs146894616 | snp | C/T | 0.000691722 | 0.0185845 | missense | UBAP2 | GRCh38.p7 | 9:33944498 | GTGGAGGGACTGTCT[C/T]CAGGTGTTGATTCTC | 55833 |
rs146922457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034992 | AAACTTCATGTTCTA[C/T]CTTGTAAGCAACAAC | 55833 |
rs146995680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996498 | TTATTTTTTTGTGGC[A/C]ATTCCATGCATGTCT | 55833 |
rs147026685 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029538 | CTCAAAAAAAAAAAA[-/A]GAAAATGTATACATA | 55833 |
rs147066957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968594 | TGTTTTAATCATGAA[C/T]GAATATTGAACACTT | 55833 |
rs147071088 | snp | A/C/T | 0.000775853 | 0.0196806 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33988987 | CATTCTCTGCCACGA[A/C/T]TGCCGCCTCTTCCTT | 55833 |
rs147087482 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBAP2 | GRCh38.p7 | 9:33943475 | TATTTTCACTGCTTG[A/G]AGCTGATCCAAATTC | 55833 |
rs147127929 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942088 | AGAGGCAGAGGTGGG[A/C]GGATCCGGAGGTCAG | 55833 |
rs147134279 | snp | G/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927977 | GGTGGGAAGAGGCGC[G/T]CTCCACACTGGCATG | 55833 |
rs147150591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989680 | CTGTACATTTTCCCA[A/G]CATAAAGCCCTTTCC | 55833 |
rs147150653 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937971 | CACAACTACATTGTG[C/T]ATAGTTGTTTTGGGG | 55833 |
rs147150850 | snp | C/T | 0.000774026 | 0.0196574 | missense | UBAP2 | GRCh38.p7 | 9:33923478 | CTGAGGCTGGAGGGA[C/T]CTGGGGGGGCAAGCA | 55833 |
rs147185317 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004741 | GTGAGCCGAGATAGC[A/C/G]CCACTGCACTCCAGC | 55833 |
rs147195760 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928577 | CCACCTAAAAGGGCA[-/T]TGGCCTGCCACTTAT | 55833 |
rs147232416 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923355 | TCTAACCCCATGTGT[C/G/T]TCTGTCTGGGAAGTA | 55833 |
rs147258654 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969856 | GGGTGACAGAGACCC[C/T]ACCTCAAACACCCCC | 55833 |
rs147289398 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982521 | GTGCCCATTTTGTCG[C/T]CCAGATAGTTTAAAT | 55833 |
rs147319645 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986012 | GGTGACAAAGTAAGA[A/C]CCTGCATTTAATTAT | 55833 |
rs147344288 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985079 | AAAAACAAAAAATTG[A/T]ATTACCGTATGATCC | 55833 |
rs147363790 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981809 | GGAAGGAAGGAAGGG[G/T]GGAAGGGGGGAAGCG | 55833 |
rs147427812 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962735 | TAATTGCAGCATTTC[A/G]GGAGGCAGAGATGAG | 55833 |
rs147428856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046031 | CTTAGCTTTTAAGAA[C/T]GCTCCATTTACTCAA | 55833 |
rs147439213 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043759 | TCAGCCTCCCAAAGC[A/G]TTGGAATTACACGCA | 55833 |
rs147445315 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962672 | TAAATAAATAAATAA[A/T]TAAATAAATAATTAA | 55833 |
rs147467918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958479 | GCAATGGTGTGATCT[G/T]GTCTCACTGCAAGTG | 55833 |
rs147501590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025936 | CCTCAGTGAAACAGC[C/T]GCATTTTCAAGTGAT | 55833 |
rs147512879 | snp | C/G | 3.3189e-05 | 0.0040735 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927943 | GAGGTCGCTGCCGTG[C/G]AGAAGGTGGCTGAGG | 55833 |
rs147531630 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029253 | GTACATAGGGCCAGG[C/T]GTAGTGGCTCAGACC | 55833 |
rs147585966 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996754 | AATTTTTTGTCAGGG[A/T]CAATATTCCATATGC | 55833 |
rs147617593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001691 | AGTAGACTGTTAGTG[C/T]CCCTGTTGCAAGAAG | 55833 |
rs147678695 | in-del | -/C | 0.0905309 | 0.192535 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928076 | TGGCGCTTGGGCCCA[-/C]AGTCTCAAGGCTGAG | 55833 |
rs147710199 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930707 | TTGAGACCAGTCTGA[A/C]CAACATAGTGAAATC | 55833 |
rs147719472 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978896 | TGTTGCCTTTTTTGC[A/G]TTATTTTTCTTCCAT | 55833 |
rs147738834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934856 | CCAACAAGCTCAGAA[C/T]GACCAACGAATCTCC | 55833 |
rs147777365 | in-del | -/AA | 0.245631 | 0.249962 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969566 | TAAAAAAAAAAAAAG[-/AA]AGAAAGAAAGAAAAG | 55833 |
rs147786167 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034783 | GAGGCTGAGGGAGGA[G/T]AATTGCTTCAACCTG | 55833 |
rs147797089 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952608 | TTCTGATAAACTTTC[A/G]CATTTAATTGGAAAA | 55833 |
rs147817318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959815 | AATACAGACTCCCCT[C/T]TAATGAAAATATTCT | 55833 |
rs147826885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955861 | AAAAAAGTTTAACAT[A/G]ATGTCTGCAACAACT | 55833 |
rs147902308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018182 | AAAAAAAAAAAAATT[A/G]TAACCATAAGATTCC | 55833 |
rs147922406 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938992 | ATGATCCATCCAAGA[C/T]GGACAAGGGACACAA | 55833 |
rs147932220 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021997 | CACCTGTAATCCCAA[A/C]ACTTTGGGAAGCCAA | 55833 |
rs147982798 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952910 | GGTCTCGCTCTGTCA[C/T]CCAGCCTGGAGTACA | 55833 |
rs147991027 | snp | C/T | 0.000148311 | 0.00861007 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:34017074 | TTGTTTCTGTGGTTG[C/T]GTTGATTGTGCTGCT | 55833 |
rs148013823 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995355 | GAGTGAGGCTGTCTC[A/T]AAAAAATAAATAAAT | 55833 |
rs148018302 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024736 | TGCCTGTCATCTCAG[A/C]ACTTTGGGAGGCTGA | 55833 |
rs148034907 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949150 | ACAGCCTGGGCGACA[A/G]AGCAAGACTCCATCT | 55833 |
rs148071932 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019890 | TGTGCAGCCGGTCGC[A/G]GTGGCTCATATCTGT | 55833 |
rs148113281 | snp | A/G | 0.000131817 | 0.00811735 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923011 | ATCAGGTAGACCAGT[A/G]GTGCTTGAAGACACT | 55833 |
rs148116164 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007642 | GTCCTTGTATGTTTT[-/A]TTTTTATTTTTTTTG | 55833 |
rs148124568 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048239 | ACATTAAATAATGAA[C/G]TGTGATATAACCAGA | 55833 |
rs148165686 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003045 | CTGCCAGAGATCCAT[C/T]CTTTTCTTTCGTTGT | 55833 |
rs148199474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997880 | GATTTCATTGTGAGA[C/T]CTTTACTCCAAAGAA | 55833 |
rs148270408 | snp | A/G | 0.000152995 | 0.00874494 | missense | UBAP2 | GRCh38.p7 | 9:33927814 | GAGGTCACCAAGGGC[A/G]CGGCCCTGCTACTGC | 55833 |
rs148312206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045584 | TCACCATGTTGGTTA[A/G]GTTAGTCTCGAACTC | 55833 |
rs148322510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962330 | TAAGAATGGCCTACC[A/G]TGGCAATTCAGGAGA | 55833 |
rs148382050 | snp | A/T | 0.000153988 | 0.00877328 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944506 | ACTGTCTCCAGGTGT[A/T]GATTCTCGAAGTTTT | 55833 |
rs148417964 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009662 | GACAGGTCTCACTAC[A/G]TTACTCAGGCTGGTC | 55833 |
rs148427947 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014214 | CGCCTGTAATCCCAG[-/C]TGCTGGGGAGGATAA | 55833 |
rs148429448 | snp | C/T | 1.69479e-05 | 0.00291095 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932625 | CTGGTGGCTGGAGAG[C/T]GAACTAGAAGACAAA | 55833 |
rs148435829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937405 | TGAGGTCAGGAGATC[A/G]AGACCAGCCTAGCCA | 55833 |
rs148460043 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960222 | GTTGTGAGTCACTAC[A/G]CCCAGCCTAACACCT | 55833 |
rs148493909 | in-del | -/A | 0.114036 | 0.209795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981562 | CCTGCTACATTGTCC[-/A]ACTCTGATCTTGAAC | 55833 |
rs148502935 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000746 | GATAAGTGGGAGTTG[C/T]TGACATTTTTTGCAT | 55833 |
rs148593465 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944079 | CCTGGTCAAGGAACC[A/G]TGCATCCTCCAACTA | 55833 |
rs148625327 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964094 | GTACCAGTTTTTAGA[A/C]AATTTATAAATTAGC | 55833 |
rs148628711 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046849 | TTTCTCCCCATACAA[A/T]AAAAGTCACTCAGGC | 55833 |
rs148636298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932766 | GACCCATCCTCATTC[C/T]TTATCCCCACAGAGC | 55833 |
rs148637135 | snp | A/C/G | 0.0022052 | 0.0331325 | missense | UBAP2 | GRCh38.p7 | 9:33923869 | TGTAGCTATAGCCAG[A/C/G]TGGCAGTGCAGGATT | 55833 |
rs148682128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042889 | CCAGCCTGGGCAACA[C/T]AGCAAGACTCCTCTC | 55833 |
rs148710877 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037513 | TTTCATCAGTGTTTC[A/G]AAACTTAGGGTTGGC | 55833 |
rs148809531 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021659 | TTTTTTTTGAGACGG[A/G]GGCTCGCTCCATCAC | 55833 |
rs148870398 | snp | C/T | 4.96372e-05 | 0.00498158 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996209 | AACAATGCAAATCAA[C/T]TAATAATACTTACTG | 55833 |
rs148902332 | in-del | -/GGAA | 0.0234074 | 0.105621 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981856 | GGGAAAGGGAGGGAG[-/GGAA]GGAAGGAAGGAAGGA | 55833 |
rs148912893 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949024 | ACAAAAAAATTAGCC[A/G]GGAGTTTTGGCAGGC | 55833 |
rs148935468 | in-del | -/AC | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006317 | CAGAAATGTCAAGAG[-/AC]ACAGAAGAGAATGAA | 55833 |
rs148942502 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935559 | GGCATCAGCCACCCC[A/G]CCTGGCCCAAGCATC | 55833 |
rs148965519 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983041 | TGCCACCATACCCAG[A/C]TAATTTTTTTGTATT | 55833 |
rs148986402 | in-del | -/TT | 0.160347 | 0.233372 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986734 | CCCTAATTGAAAGCA[-/TT]TTCTTCCCTCTTACT | 55833 |
rs148989144 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047666 | AAAGATAATCTTTGG[A/G]TACCTTATGGAGACC | 55833 |
rs148997165 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929928 | AGAACTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 55833 |
rs148999790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044703 | AAATCCCATCTCTAC[C/T]AAAATTACAAAAATT | 55833 |
rs149057123 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001228 | AACAAATCTCTAAGT[-/A]AAAAAGGTTTTATTT | 55833 |
rs149073413 | in-del | -/AAG | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940061 | GAGAGGGAGAGGGGA[-/AAG]AAGAAGAAAAGAAAA | 55833 |
rs149123312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988534 | TACCATGAGTGTCTA[C/T]AAATGGAGAATATAA | 55833 |
rs149157462 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013013 | ACTAAAATTAGCCGG[A/G]TGTGGTGATGTACAA | 55833 |
rs149161309 | snp | A/G | 4.9579e-05 | 0.00497866 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927846 | GCTGGATGCACTCGC[A/G]GGGGTCCCACCCAGA | 55833 |
rs149166426 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026561 | GGCAAGGATGGGTCT[C/G]AGGTCCTTCATCTAT | 55833 |
rs149177545 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939987 | ATAAGGTAGGAGGGA[A/G]GAGGGTGAGGAGGAG | 55833 |
rs149184570 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018880 | ATAAATAAATAAATT[-/AAAA]TTAAAAATAAAAAAT | 55833 |
rs149185581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962092 | CAGAATTGTAAGAGA[A/G]AGCTTGATGGCGAAG | 55833 |
rs149261647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937261 | GGTTCAATTTAACTG[C/T]GTCTGGGGTGTAAAT | 55833 |
rs149316845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931862 | GCCCAACACCTCCTG[C/T]TGTCCAGGAGCATGC | 55833 |
rs149349822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957809 | ACTTCCTGCATGACA[C/T]ACTATGTGTAAGCAG | 55833 |
rs149403635 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969565 | TTAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 55833 |
rs149408613 | snp | A/G | 1.74741e-05 | 0.0029558 | missense | UBAP2 | GRCh38.p7 | 9:33922875 | ATCCCTGCTTGTCAA[A/G]AGTCTACAGGGCAAA | 55833 |
rs149431709 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990877 | CCTGACCTCAGGTGA[A/T]CCACCTACCTCGGCC | 55833 |
rs149441020 | snp | C/T | 0.0015522 | 0.0278153 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998849 | CTTGAGCGAGACGCA[C/T]CTGTTCAGCTGTTGC | 55833 |
rs149475371 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981516 | GCACATCATCATGCC[C/T]GGCTAATTTTTTTTT | 55833 |
rs149520012 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015191 | GTTTGCCAATCTAGT[C/T]AATAACATGTATATA | 55833 |
rs149527021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975661 | AAAAAGAAAAATTAG[C/T]CAGGCGTAGTGGCAG | 55833 |
rs149603696 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039022 | CCGACCCGTCTGAGA[A/G]GTGAGGAGCCCCTCC | 55833 |
rs149643527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950893 | AAATGTATACAATAC[A/C]CACATGTGCATACAT | 55833 |
rs149655708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044602 | AGGTGTGGTGGCTCA[C/T]GCAAGTAATCCCAGC | 55833 |
rs149666611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929193 | CTCTGACCAGTGCTC[A/G]CAAGTGTACTTGGAT | 55833 |
rs149670277 | snp | C/T | 1.65839e-05 | 0.00287953 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932577 | TGTGTGTGACGTGCT[C/T]GAGGAGAGGGCTGCA | 55833 |
rs149675927 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978716 | ACCCAGGAGGGGGAG[C/T]GTGCAATGAGCCGAG | 55833 |
rs149718083 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009245 | CTGGGATTACAGGTG[C/T]ACACCACCACGGCCA | 55833 |
rs149718230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924337 | CTGCTTGACTCCCAG[G/T]AGAGCAGAACCAGCA | 55833 |
rs149748843 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995055 | AAAATAGTTTCCTCA[A/G]TTTAAGAAACATAAA | 55833 |
rs149804576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030048 | GCTCACGCCTGTAAT[C/T]CCAACACTTTGAGAG | 55833 |
rs149832163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982746 | TAACTTTTATTTATT[C/T]GGGGTTTATTAGTCT | 55833 |
rs149865443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006458 | GCTGAGGCAGGCAGA[C/T]TGCTCGAGCTCAGGC | 55833 |
rs149886991 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBAP2, SNORD121B | GRCh38.p7 | 9:33934351 | CAGATATGTGCTTGG[A/C]AATAAAACATCATTG | 55833 |
rs149887417 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021006 | GCAAGCATTCCCATG[A/C]TGTGGAAAGATATTC | 55833 |
rs149927922 | snp | A/G | 4.9708e-05 | 0.00498513 | missense, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33963736 | CATACCTTTGAGTCC[A/G]TAAGAACTTTTGTTT | 55833 |
rs149936354 | snp | A/G | 3.2987e-05 | 0.00406108 | missense | UBAP2 | GRCh38.p7 | 9:33926628 | TCACCACTGGCAGCC[A/G]TGACTGCAGCATCTG | 55833 |
rs149962543 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034214 | GACAGTTACATCATC[C/T]CTAGGTTTTATTACA | 55833 |
rs149988578 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995352 | GCAGAGTGAGGCTGT[C/G]TCAAAAAAATAAATA | 55833 |
rs150045065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939519 | TGTGTTTTTAATGCT[C/G]TCAGCCATTTGTGTG | 55833 |
rs150063175 | in-del | -/AGCGGCGGTGGTGGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016365 | GGCAGCAGCGGCGGC[-/AGCGGCGGTGGTGGT]GGTGGTGGTGGTGGT | 55833 |
rs150108118 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030723 | CAAGGTCAGGTGATC[A/G]AGACCATCCTGACTA | 55833 |
rs150112529 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034888 | AACAAACAAACAAAC[A/C]AAAAAAAAACGAATC | 55833 |
rs150153562 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984672 | AACAGAGTGAGACAC[G/T]GTCTCTTAAGAGAAA | 55833 |
rs150194348 | snp | C/T | 0.00159669 | 0.0282099 | missense | UBAP2 | GRCh38.p7 | 9:33941798 | TGCAGGAGGTAATGA[C/T]GGAAGTTGTATATGT | 55833 |
rs150234878 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967270 | CTTTTACACAATCAC[A/G]AAAAACAACGGTTTA | 55833 |
rs150236972 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047463 | ATGTAGGATACGGGA[C/G]AGCTTAGGTATCATG | 55833 |
rs150267349 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036097 | AATTTAATTGTAACT[C/T]CAGGAATTTGATACT | 55833 |
rs150275904 | snp | A/G | 0.00194564 | 0.0311293 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953296 | TTACCAGGCTCTGAG[A/G]AGAACAGGAGTTGAC | 55833 |
rs150277070 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921631 | TGGGATCTCCTTTAG[A/C]CCTGTGAAGTCCAGG | 55833 |
rs150329837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956278 | TAAAGAAAATGAAAT[A/C]TACAAGTGACCATGA | 55833 |
rs150361628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941518 | AACAAACTCAATGAA[C/T]TATAAGGATTCTACT | 55833 |
rs150391628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931583 | GCAGAGGTGTCCACA[C/T]TATGCTCTCCTTTGA | 55833 |
rs150445503 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012679 | AGAAGAACCTTATTC[A/G]CAACTACTTGTCAAA | 55833 |
rs150452276 | in-del | -/TAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962653 | ATCTCAAAAATAAAT[-/TAAA]AAATAAATAAATAAA | 55833 |
rs150454116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926396 | CCCAGGTCCCAAAGG[C/T]CTTCATGTTTCCCAG | 55833 |
rs150495223 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027174 | CCTGCAGAAGACAAA[A/G]CTCAGATTAAGAATC | 55833 |
rs150502298 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978571 | AGATCAGGAGATCAG[A/G]AGATCAAGACCATCC | 55833 |
rs150510020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024818 | GCGAAACCCTGTCTC[A/T]ACTAAAACTACAAAA | 55833 |
rs150554280 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970371 | TACAGTTGGTTAGTC[A/G]TGCTTCTGGTGGTAC | 55833 |
rs150554466 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049881 | ATCTGACCTGTTGTC[A/T]ACTCCAAGAATTACG | 55833 |
rs150584039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923689 | AAGACCAGGTAAGAC[A/G]GAGTGGAATCACAAC | 55833 |
rs150585778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037691 | ACCTGACTGGCAATT[A/G]TATCTGATAAATAAT | 55833 |
rs150606183 | snp | A/C | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007868 | AGATGGTCTCTATCT[A/C]CTGACCTCATGATCT | 55833 |
rs150636902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957513 | TCATAAAAGTATCCA[A/C]ACCTTTATTCCTGGC | 55833 |
rs150662040 | snp | C/T | 1.80455e-05 | 0.00300373 | missense | UBAP2 | GRCh38.p7 | 9:33922775 | AATGGTGGGGGTGCA[C/T]AGCCAGGGGCCGCTC | 55833 |
rs150669989 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029783 | TCATGAGATCAGGAG[C/T]TCGAGATCAGCCTGG | 55833 |
rs150677719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944790 | GTAACACTTCATTTA[C/T]GATAAACGGGAAAAG | 55833 |
rs150707138 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934047 | GCTAACAGGCAAGAC[C/T]ACCTACACGTGCTTC | 55833 |
rs150720796 | snp | A/G | 1.68766e-05 | 0.00290483 | missense | UBAP2 | GRCh38.p7 | 9:33944637 | CAGGTTGAGATTTGA[A/G]GTCTAAAAAAAGTAA | 55833 |
rs150731122 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949803 | AAAATGAGACACTGC[A/G]ATACATAGGTATTTG | 55833 |
rs150817609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045942 | TGTATCTCCACTCTT[C/T]GGAAAAAACGGCTGC | 55833 |
rs150840669 | in-del | -/AAAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949191 | ATAAATAAATAAATA[-/AAAAT]AAAATAAAATAATAA | 55833 |
rs150842629 | in-del | -/AG | 1.67522e-05 | 0.0028941 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943620 | TGTCGTGTCAGGAAC[-/AG]AGGTCACAGATTCCA | 55833 |
rs150880434 | snp | C/T | 0.000839969 | 0.0204763 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986709 | AGCAACGCAACTGCC[C/T]GCTTCTTCCCCCTAA | 55833 |
rs150980034 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929155 | CAGACTCCCCACCAA[-/C]CTGCCACAGAAATCT | 55833 |
rs150987720 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030406 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 55833 |
rs151027666 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935665 | TCTTGCTGTGGTTAA[C/G]ACATTTCTAATAACA | 55833 |
rs151038448 | snp | A/T | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951563 | CATTGGCCAGGCTGG[A/T]CTCAAACTCCTGACC | 55833 |
rs151124093 | snp | A/G | 0.00239568 | 0.0345268 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017460 | TTTATCACTACATGT[A/G]GTCACTGTACATGAA | 55833 |
rs151191223 | snp | C/T | 4.94279e-05 | 0.00497107 | missense | UBAP2 | GRCh38.p7 | 9:33923976 | GGGGATGCAGAGTCC[C/T]CACGGCCAAACTTTG | 55833 |
rs151210871 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034887 | AAACAAACAAACAAA[A/C]AAAAAAAAAACGAAT | 55833 |
rs151220060 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001188 | CAACTTGTTATGAAC[C/T]GTTAAAGTCAAAAAT | 55833 |
rs151251319 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993096 | ATGAAACAAAAAGTT[A/C]AGTACTTATGTTCAA | 55833 |
rs151252793 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027502 | GGGGGAGGATCGCCT[C/G]AGCCCAGGAGTTTAA | 55833 |
rs151291929 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973741 | TCTCTTCATTAAAAT[C/G]CTAAACTGAAGAGCA | 55833 |
rs151321203 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925521 | TGCTGTGAATAAGTG[C/T]GGAGACCACGGAGAG | 55833 |
rs180724996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032309 | CTCATAGATTTAATA[C/T]CAACAGCACAATAAC | 55833 |
rs180791686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000431 | ACTTTGTAATGTGCC[A/G]GTCTGGTTTCTTAGT | 55833 |
rs180850064 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995448 | ACAAATATTATAAAT[A/G]TTATATATAATATAT | 55833 |
rs180855893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030167 | ATCAGCCAGGTGAGC[C/T]GGGCGCGGTGGCTCA | 55833 |
rs180858035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014719 | AGAATCACTTGAACC[C/T]GGGAAGTGGAGGTTG | 55833 |
rs180868278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036606 | GTAAGCAACTGAAGA[C/T]CAGGAACCTACATTA | 55833 |
rs180874563 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048536 | GCAGAAACCCGAAAG[G/T]GGGGAGGGGAGGCAC | 55833 |
rs180921272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941364 | AAATATTCAGAGATA[C/T]TTCAGACAATGTAGA | 55833 |
rs180932259 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966251 | TCAAGAGTTCAATAC[C/G/T]TACCTGCCCAACATG | 55833 |
rs180955002 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977449 | CGCTACTAGTAACAT[C/T]GGTTTCTGTGTATAT | 55833 |
rs180962007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003220 | GGTTTTGGTAGAGAC[A/G]GGGTTTCACCATGTT | 55833 |
rs180982480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985076 | ATCAAAAACAAAAAA[C/T]TGAATTACCGTATGA | 55833 |
rs180993832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021831 | TAGAGATGGGGTCTC[A/G]ACTTGTTGGTCAGGC | 55833 |
rs181125903 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980492 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 55833 |
rs181130623 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBAP2, SNORD121B | GRCh38.p7 | 9:33934342 | CATACAACTCAGATA[G/T]GTGCTTGGAAATAAA | 55833 |
rs181134442 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957991 | CAGACCTTAGTCTGT[C/G]ACCCAGGCAAGAATG | 55833 |
rs181174692 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017649 | AACAATTGTGTGGCC[C/G]GGTGCGGTGGCTCAC | 55833 |
rs181182924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031954 | CCAGCCTGGGTAACA[C/T]AGCAAGACCTCCTCA | 55833 |
rs181234484 | snp | A/C/G/T | 4.95647e-05 | 0.004978 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998846 | TCACTTGAGCGAGAC[A/C/G/T]CATCTGTTCAGCTGT | 55833 |
rs181275862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027317 | GAAACCCTACCCTAC[C/T]AAAAATACAAAAAAT | 55833 |
rs181278295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952635 | AAAACAAGAAATTGA[A/T]TATACTAACTATAGA | 55833 |
rs181295922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977036 | AAAAACAGTTGTTTT[C/T]TATTTATTTTTTTTT | 55833 |
rs181302044 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014590 | ACTGAGATGGCACCA[C/T]TGCACTCCAGCCTGG | 55833 |
rs181304971 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995128 | TTGGGAGGCCAAGAC[A/G]GGTGGATCACCTGAG | 55833 |
rs181352327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930019 | CAGAAAAATAATAAG[A/G]AATAAATAAATAAAA | 55833 |
rs181363706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043332 | ACACCATGCCCAGCT[A/G]ATTTTTGTATTTTTA | 55833 |
rs181368980 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984344 | TAAACAACTCAACAG[A/C]CAAAATATAAATAAT | 55833 |
rs181465021 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940917 | AGGAAACCAAAAAAT[G/T]AGCGCAACTTTCTTT | 55833 |
rs181514440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046823 | CTACATGTTCTCACA[C/T]CATCACACCATTTCT | 55833 |
rs181583354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957614 | TAAATTTTTTGAAAC[C/G]TCAACTGACATTAAT | 55833 |
rs181592400 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980443 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGGTGG | 55833 |
rs181599702 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965096 | TAATTAACTTTTTAT[C/T]TTAAAATAATTATAG | 55833 |
rs181600224 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027718 | AAAAAAAAATTAGCC[A/G]GGGGTGGTGGCGGGT | 55833 |
rs181602542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016878 | CTACTGTTTAAACAA[A/G]GGGTCCAAAATCCTA | 55833 |
rs181608372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998392 | AACAGAGTGAGACCA[C/T]GTCTCTATGAAAAAA | 55833 |
rs181615569 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031612 | ACGCCCGGCCTTAAC[G/T]TGCTTTCCTAAGTAA | 55833 |
rs181728167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008498 | CCTGTAATCTCAGCA[C/T]TTTGGGAGGCTGAGG | 55833 |
rs181771889 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925982 | CCACAGTTCTGTTCA[C/T]GTGGCTATCCCAGGA | 55833 |
rs181795355 | snp | A/G | 3.30322e-05 | 0.00406387 | missense | UBAP2 | GRCh38.p7 | 9:33941650 | AAAATACCACTTACC[A/G]TGATGGTTCCTGGAG | 55833 |
rs181799118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972834 | GTGCCATTTAGGTAC[A/G]TCTATAGGTATTTTG | 55833 |
rs181890577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985314 | GATATCCGTTACCAT[A/G]AGCATTTATCATTTC | 55833 |
rs181900898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003736 | TTCTTTTGTTTTTTT[C/T]TGAGACAGAGTTTCA | 55833 |
rs181913901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023148 | GAAGAATCGCTTGAA[C/T]CCAGGAGGCAGAGGT | 55833 |
rs181918552 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037903 | TACAGCAGCTGCTCA[C/T]GCCTATAATCCCAAC | 55833 |
rs181927520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026413 | GATGACATGAATTAC[A/G]TAATGGGCTAAGGGT | 55833 |
rs181942951 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951638 | AGGTGTGAGCCACCG[C/T]GCCCAGCTCCCAGTG | 55833 |
rs181951358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994611 | CAGGATACTTAGTCC[C/T]AGGTCAGTAAACAAA | 55833 |
rs182002819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971902 | TTCCCCTATTTAAAT[A/G]TAACTAATTCTGCCA | 55833 |
rs182011889 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959001 | TAAAAATACAAACAT[C/T]GGCCAGGCATGGTGG | 55833 |
rs182013613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008030 | TTTAAAAGAGGGCCA[C/G]AGGCTGAGGCAGGAG | 55833 |
rs182018615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989628 | GCTAAGCTCCTGTTG[C/T]TAAATAATTACAGCT | 55833 |
rs182019029 | snp | A/G | 3.74693e-05 | 0.00432819 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935686 | TCTAATAACACCACA[A/G]CCAACACCTGGTCCA | 55833 |
rs182020239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025688 | ACAAAGATATTCTCT[A/G]TGAAAGGAATAGTTT | 55833 |
rs182033719 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041478 | TCAAAAAAAAAAAAA[A/C]AAACAAACAAGAGTC | 55833 |
rs182067640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947900 | CATCTATAATCCCAG[G/T]TACTCAGAAGGCTGA | 55833 |
rs182070975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028662 | TGGGATTACAGACAC[A/G]AGCCACTGCGACCAG | 55833 |
rs182073648 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990094 | CTGAGAAAGAAAAAG[A/T]TACTACATTCTTGAC | 55833 |
rs182078087 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946615 | GCCCAGGCTGGTCTC[A/G]AACTCCTGCTCAAGC | 55833 |
rs182085789 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010772 | ACAAACATTTTTTTT[A/T]AAAAAGTAAAATTAT | 55833 |
rs182087769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991881 | TTACACAGCCTCGCC[A/G]AAAGGTACTCTATCT | 55833 |
rs182095344 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027633 | GAGGCCAAGGCAGGC[A/G]AGTCATGAGGTCAAG | 55833 |
rs182105480 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044136 | GGCGCGGTGACTCAC[A/G]CCTGTAATCCCAGCA | 55833 |
rs182201417 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929534 | CCTTTATGTATTGAT[A/G]GAGAGTGGTAAAGAT | 55833 |
rs182205342 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966983 | TCAGTAAAAACTAAA[C/T]GTCACAACAGTGGGA | 55833 |
rs182217810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987049 | TTCCAGCACTTGTAA[C/T]TTCCAGCTGAGGGGG | 55833 |
rs182218773 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976231 | AGCTACAAAACAAGG[A/G]AACTATTCTCAGGAC | 55833 |
rs182247866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981429 | GGCACAATCACAGCT[C/T]ACAGCAGCCTCAACT | 55833 |
rs182254923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017761 | GAAACCCCGTCTCTA[C/G]TAAAAATACAAAAAA | 55833 |
rs182354238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013433 | GAGGCAGAGGTTGCA[A/G]TGAGCTGACATCGCA | 55833 |
rs182365603 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045435 | CTGGATGAAGTCCAA[G/T]GGCACATGGCTCACA | 55833 |
rs182392157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927420 | GCAGTGCCAGGAGAG[A/G]GACAGGCTGAGTTCG | 55833 |
rs182449762 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020006 | CTCTACTAAAAATAC[A/G]AAAATTAGCCAGGCA | 55833 |
rs182489443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948259 | AAACTGCAAGAGTTC[C/T]ACTAAAAAGAAACAT | 55833 |
rs182497518 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990826 | AATTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 55833 |
rs182504659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973106 | GATGACTAAATTAGA[C/T]GTAGGGTATTAGAAG | 55833 |
rs182508101 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008896 | CTTGAACCCACAAGG[C/T]AGAGGTTGCAGTGAG | 55833 |
rs182546047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999083 | ATTCCTTTGACCAAA[C/T]GACCTAAAGCTATTG | 55833 |
rs182580922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924521 | TCACCAGGCAGAGCT[A/G]CTGGAGACCAAGCCT | 55833 |
rs182598568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033236 | CTATCAACAGGTGAA[C/T]AGATAAAACATGGTA | 55833 |
rs182609032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004933 | TAAAACATTTAAAAA[C/T]CAGACACTTCTTGCA | 55833 |
rs182620616 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038937 | CTGCCCCGCCACCCC[A/G]TCTGGGATGTGAGGA | 55833 |
rs182661164 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930656 | TAATCCCACCACTTT[G/T]GGAGGCCGAGGCGGG | 55833 |
rs182729638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033731 | TACAGTCAAGCATCA[A/G]ATCAATTCTTTTTTT | 55833 |
rs182791545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931702 | ATCCAGAGGAAAGGA[C/T]AGGATGTCCCTTTTC | 55833 |
rs182800634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955804 | TGCACTCTAGCCTGG[C/G]CAACAAGAGCAAAAC | 55833 |
rs182892785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023930 | GCACCTGTAGTCCCA[A/G]CTACCCAGGAGGCTG | 55833 |
rs182900893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978605 | CTAACACAGTGAAAC[C/T]CCATCTCTACTAAAA | 55833 |
rs182913357 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038679 | CTCCCAAAGTGCCGA[A/G]ATTGTAGCCTCTGCC | 55833 |
rs182918612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016100 | GGGAGAAAAGGGAGA[G/T]GAGATGATGATGAAG | 55833 |
rs182918820 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996561 | TCAATCTTCCTCCAA[C/G]TTGACCAAGGAGCAG | 55833 |
rs182925386 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030403 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 55833 |
rs182949210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953149 | GCTGGGATTACAGGC[A/T]TGAGCCATCATGCCC | 55833 |
rs182979091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960733 | TGCAATGAGCCAAGA[C/T]CACGCCATTGCATTC | 55833 |
rs182989459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000345 | CATTACTGACTGAAG[G/T]TTCGTTTTCTGATGT | 55833 |
rs183043008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982479 | TTTATATAAAGCGAA[C/T]GTAATAGATTTTGAC | 55833 |
rs183048809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959870 | GGCAACAGTGTCAGC[C/T]GGCTATCAGGTCAAA | 55833 |
rs183056802 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999984 | ATGGAGTCTCACTCT[G/T]TCGCCCAGGCTGGAG | 55833 |
rs183063939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032795 | TGGGCGTGGTTGCAC[A/G]CACCTGTAATCTCAG | 55833 |
rs183064053 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018453 | AATGGTGGTTCCTTA[A/T]AAAAAAAAAATCAAA | 55833 |
rs183103534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937274 | TGCGTCTGGGGTGTA[A/G]ATAAGTAAAATTATC | 55833 |
rs183116963 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942841 | AAATTAGATCCCTCA[C/T]AGACTACTGGTAGGA | 55833 |
rs183145862 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985998 | TGCACTCCAGCCTGG[A/G]TGACAAAGTAAGACC | 55833 |
rs183158797 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006578 | CTACTCAAGAGGCTG[A/C]GGTAGGAGGATTATC | 55833 |
rs183161681 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987626 | AAAAAGTGAAAAAAA[A/T]ATATATATATGAAAT | 55833 |
rs183172422 | snp | A/G/T | 0.021333 | 0.101051 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019174 | GGGAAGAGGAGGCAG[A/G/T]TAGATTGATTACAAG | 55833 |
rs183173104 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024269 | ATCGCTTGAACCCGG[A/G]AGGAAGAGGTTGCGG | 55833 |
rs183232341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968824 | ACTCCATACTCATTT[A/G]TAGTCACTCACCACT | 55833 |
rs183234680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937664 | TGTAATCCTGGCACG[C/T]TGGGCAGCTGTGGTG | 55833 |
rs183275326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982635 | CAGTCCCAGTAAGAA[C/T]AGGAAGAACAGGTCA | 55833 |
rs183292117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023547 | ATCTCCTTCCAATCA[C/T]CAATTCTTAATATTC | 55833 |
rs183320868 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049173 | GGTGCCCACAACTGC[A/G]GCTCGTCGTCGCGCC | 55833 |
rs183344547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931483 | AGGCAGCAGTGGCAC[A/G]GACACAGAGGACAGC | 55833 |
rs183398514 | snp | A/T | 0.0143191 | 0.0833936 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966903 | AAATCTAATTTTTTT[A/T]AAAAATCAGTGGGGA | 55833 |
rs183441177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974563 | AGGCAACCCAAAGAA[A/T]GGAAGAAAATATTTA | 55833 |
rs183447355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928219 | ATAAACTGAACATCA[A/G]AACTATTAACATTAA | 55833 |
rs183485408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011081 | AAACCAAAGAAACAC[C/T]GACCCGATTAAAATA | 55833 |
rs183497245 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962934 | CAGTGAGCCGAGATC[G/T]CACCATTGCACTCCA | 55833 |
rs183508792 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939826 | AGGGGAGGAGGAAGG[A/G]GGGGAGGAGGGGGAG | 55833 |
rs183510573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983100 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 55833 |
rs183535337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004042 | TAGCTTTCTAACAAT[C/G]AATACAAAGAAGTAA | 55833 |
rs183596037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044305 | ACTCGGGAGGCTGAG[C/G]CAGGAGAATGGCGTG | 55833 |
rs183599391 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028361 | AGCTGTAAACCCTGT[A/C]TTATTTATTTATTTA | 55833 |
rs183602015 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013346 | CCTGAAGTCAGGAAT[G/T]CAAGACCAGCCTGAC | 55833 |
rs183621713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045295 | AGCTTGAAGTGAGCC[A/G]AGATTGCACCACTGC | 55833 |
rs183701417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949428 | ACAGGTCAGGCTGGG[C/T]GCAGTGGCTCACACC | 55833 |
rs183707021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992943 | GTCTTCGAAGCCAGC[C/T]AGTTCAAAAATTACT | 55833 |
rs183781965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030366 | AGGCAGGAGAATGGC[A/G]TGAACCCGGAAGGCG | 55833 |
rs183816791 | snp | A/T | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027691 | CGAAACCCCATCTCT[A/T]CTAAAAATACAAAAA | 55833 |
rs183823977 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946095 | GTGGAAAATGGTATT[A/T]AAAAATACAAACTAA | 55833 |
rs183834546 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955498 | GCACTCCAGCCTAGG[A/C/T]GACAGAGTGAGACTC | 55833 |
rs183839006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923692 | ACCAGGTAAGACGGA[A/G]TGGAATCACAACCCT | 55833 |
rs183844396 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995845 | CATATACCAGCAAAT[C/T]CTGGTTTTCTGTTAT | 55833 |
rs183930076 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988763 | TTCTAGTGTTAACTA[G/T]TAGAACAAATTCTGC | 55833 |
rs183936290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970763 | TATATTCTAAGTCTA[A/G]GTTATAATTCATTGT | 55833 |
rs183938457 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016251 | AGGGGAGGAAGAGGA[A/G]GAGGAGGAAGAGGAG | 55833 |
rs183947827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030978 | GGCTAGGCACTGTAG[C/T]TCCTGCCTATAATCC | 55833 |
rs183952470 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050235 | CCTGTTTTATCCCAA[A/G]CTAGTTACATACAAG | 55833 |
rs184025721 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949113 | CGGAGCTTGTAGTGA[C/G]CAGAGATCACGCCAC | 55833 |
rs184036255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978112 | ATAGAGGCACAATAA[C/T]GGCATTATATAATTA | 55833 |
rs184037864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015323 | ATTTTATTCAAATGG[G/T]TCTTTGTTTTATTGA | 55833 |
rs184048081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944305 | ACTTAGTATCCCACT[A/G]GAGCTGAATGTAAAA | 55833 |
rs184076710 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975097 | ATCCCATATTCATTC[A/G]GATGACTACTACCAA | 55833 |
rs184083161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012754 | AGTAGATGTGACAGA[A/C]ATGTTAAAATCTGGG | 55833 |
rs184089362 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993573 | GCTACTCGGCAGGCT[A/G]GAGGATGGCATAAGC | 55833 |
rs184105770 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027841 | CACTCCAGGCTGGGC[A/G]ACAGAGCGAGACTCC | 55833 |
rs184160166 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950455 | CAATTACTTCTATTA[C/T]CAACATTCAAAGACA | 55833 |
rs184175739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928636 | AAAGAGTGAACCAGC[A/G]GATGCTCCATCAGCC | 55833 |
rs184177766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998492 | AGATATACTTTCTAT[A/G]CACAGGTATCGGAAA | 55833 |
rs184184909 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016988 | CACATACCCTAAAAC[C/T]TCAAGTATAATAATA | 55833 |
rs184185993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031811 | AAAAAAAAGAAAGAA[A/G]AAAAGAGGATCTATT | 55833 |
rs184187971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927602 | AAAAGCTAGAAGCAC[A/G]CAGAGGCCAGGAATC | 55833 |
rs184189206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973494 | AGCTAAACACAGGGA[G/T]GTTGTATTATAAAAC | 55833 |
rs184207515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994032 | CCTGAGTAGCTGGGA[C/T]TGCAGGCGCCCACCA | 55833 |
rs184229480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957697 | GCTGGAAAATGTTGA[C/T]CTAATGAGGTAACAC | 55833 |
rs184242747 | snp | C/G | 0.000158076 | 0.00888894 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933465 | CCAAGGTACTTCTCA[C/G]TTTGGGCCCACACCT | 55833 |
rs184242842 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980448 | GGGTTTCACCGTGTT[A/G]GCCAGGGTGGTCTCG | 55833 |
rs184299900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929009 | AAGACAGCCAAAAAC[A/G]TGGTTTCCTGGGGCT | 55833 |
rs184327497 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939732 | AAAATGAAGAAGAGA[A/G]GGAGAGGGAGGGAGA | 55833 |
rs184330250 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975490 | TGGAGCACACCATTG[A/T]GCACTGCTGGTAAAA | 55833 |
rs184332211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000921 | GACATTGGTACAGAA[A/G]TTCAGTGTCTACCCT | 55833 |
rs184358189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932263 | TCAGGAAAGAAGGCA[C/T]GAGGAAAGATCAAAC | 55833 |
rs184372296 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983696 | CTTCAGGGTTTAGGA[A/C/G]CTAATAAATTAGCAG | 55833 |
rs184378046 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978784 | GACTACGTCTCAAAA[A/G]AAAGAAAGAAAGAAA | 55833 |
rs184378952 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964501 | AACATTCGGCTTCAA[A/C]GCCATGGAAGCCAGC | 55833 |
rs184467251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002082 | TGACCTCAGCCTCCT[A/G]AGTAGCAACCATGGC | 55833 |
rs184483713 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034994 | ACTTCATGTTCTATC[C/T]TGTAAGCAACAACTA | 55833 |
rs184487892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020191 | GAGATAAACACACAC[A/G]TTAGTCTAGGCCTAC | 55833 |
rs184510567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956581 | TGATGCACCCACCTT[C/G]ACCTCCCAAAGTGTT | 55833 |
rs184514684 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997251 | TTACTTAGCATTTTC[A/T]TCACTAGAACGATCA | 55833 |
rs184530883 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040930 | GTGGAAAACACTTTA[A/G]CATTACTTAGTAAAA | 55833 |
rs184615389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957113 | AAAAGAAGAAGTCAT[C/T]AAGAAGTTTGTAAAG | 55833 |
rs184665406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965820 | CTGAGAGGCCGAGGC[A/G]GGTAGATCACAAGGT | 55833 |
rs184667723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025240 | AACAAGTACCCAGTT[A/G]CCAGACCATAGGAAT | 55833 |
rs184677099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002437 | AGGCTGGAGTGCATG[A/G]CGCGATATCGGCTCA | 55833 |
rs184695466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932815 | TGGACGGGAATGACT[C/T]GCCATGAGGTCTGGA | 55833 |
rs184813304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941048 | CTAGTGTGACATGAA[A/G]TGTGTATACTTGTTC | 55833 |
rs184818314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984433 | TTTGGGACACTGAGG[C/T]AGGAGGACAGCTTGA | 55833 |
rs184826611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021127 | AGAGGAGACTAACCA[C/T]AATTCATCATACTAA | 55833 |
rs184826878 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044589 | AAAAGAAGAAGCCAG[A/G]TGTGGTGGCTCACGC | 55833 |
rs184829164 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036144 | TTTGAGACGGAGTTT[C/T]ACTCTTGTTGCCCAG | 55833 |
rs184924552 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030208 | CCCAGCACTTTGGGA[A/G]GCTGAGGCGGGCAGA | 55833 |
rs184976289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041681 | CTGGCATTCCAGCCT[A/G]GGCAAAAGAGCAAGA | 55833 |
rs185042708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048601 | GGGGGAAAGTAGGAA[A/G]AAGCACAGGGCAACG | 55833 |
rs185057156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988222 | AAAGTTTTAGAAAGG[C/T]AAAGATTTTACTTAC | 55833 |
rs185063056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024530 | AGTCTTAATATTAAA[C/G]ATGTCCAGCAAAAAA | 55833 |
rs185092685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039887 | ATACAAGCCGCACAC[A/G]GTGGCTCACGTCTGT | 55833 |
rs185120384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985171 | CAGGTTGTGGTGGCT[A/G]TGGCAATTTCTATTT | 55833 |
rs185137556 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003439 | TGCAGTGGCGTGATC[A/G/T]CGACTCACTGCAACC | 55833 |
rs185146719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970203 | CTCCTAATATCTATA[C/T]GATCCATATCAATAT | 55833 |
rs185150870 | snp | A/G | 0.00140238 | 0.0264428 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922625 | GGAGAAGGGAAGGCT[A/G]TCAAGGCTGGAGCAG | 55833 |
rs185175580 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009379 | GCTGGGATTACAGAC[A/G]CAAGCCACCACACCT | 55833 |
rs185177060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007176 | TTTCCTTCTCTTGCC[C/T]ATTTGCTCTGGCTAG | 55833 |
rs185177185 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031987 | TCTACTAAAAAATAC[A/G]TTTAAAAATTAGCCA | 55833 |
rs185181683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991423 | GGAGACTAAGTAGTC[C/T]AGTGTATCCATAAAT | 55833 |
rs185193368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941416 | AGTGCTCATACTACA[C/T]GCATGCTTGGTTTTC | 55833 |
rs185193748 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027487 | TCTGGGAGGCCAAGA[A/G]GGGGAGGATCGCCTG | 55833 |
rs185214402 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940295 | AAATGTGTGTGTGAG[G/T]GTGTATACACCCTAG | 55833 |
rs185231825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927452 | AGTCGGTTTTAGCAG[C/T]GACCATCAAATCATA | 55833 |
rs185249054 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | UBAP2 | GRCh38.p7 | 9:33948500 | GGCCCAAACTCGGAG[C/T]TTTCAACTGGTCCAA | 55833 |
rs185264314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973336 | CCCAGACAATATTAT[C/T]ATTATTCCTAGTAGC | 55833 |
rs185344412 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014061 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 55833 |
rs185361346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045514 | GAGCAGCTGGGACTA[C/T]AGGCACGCGCCACCA | 55833 |
rs185395897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952709 | AAAGGGGTACTTTCA[A/G]TCTCAAGAGTGATCA | 55833 |
rs185406751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930068 | ATAAAGGAAATCAAA[C/T]GGTTTTCAAATATAT | 55833 |
rs185411742 | snp | A/C/G | 0.0895908 | 0.192291 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977223 | TTTGTATTTTTATTA[A/C/G]AGACGGGGTTTCACC | 55833 |
rs185449948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994998 | TGATGTGTTCATCTT[C/T]GTATCCTCTTTTAGG | 55833 |
rs185482567 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028928 | AGCAAACCTGGGCGG[C/T]GTGGCAAGTCCTCGT | 55833 |
rs185493416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997951 | CACTGAGGTAGCGGT[A/T]ACAGCTTGGTTTCTA | 55833 |
rs185506260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031149 | CGGGCATGGTGGCAC[A/G]GACCTGTAATCCTAC | 55833 |
rs185516348 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922209 | GAAGACCTGAAGGCA[A/G]ATGGGGTGGGGGTGC | 55833 |
rs185525601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014636 | TCCATCTCGAAGAAA[C/T]AAAAAAAAATTAGGC | 55833 |
rs185528485 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995225 | AGCTGGTCGTGGTGG[C/T]GCATGCCTGTAGTAC | 55833 |
rs185535892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029825 | AAAACCCATCTCTAC[C/T]AAAAATACAAAAATT | 55833 |
rs185548771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048386 | GCGCATAAGTTGGGG[A/C]TATAACAGGGCCAGT | 55833 |
rs185608097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979714 | GGTGAAACCCCGTCT[C/T]TACTAAAAAATACAA | 55833 |
rs185614405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016712 | AGGCGCACACCACCA[C/G]GCCCAGCTAATTTTT | 55833 |
rs185750672 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926293 | GTCTTGTGTCATATG[G/T]TTTTTCTTTTTAAAA | 55833 |
rs185781383 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995572 | AATTTAATTTAATTT[A/G]AAATTAAATTATTTA | 55833 |
rs185787405 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022232 | CCTGGGCAACAAGAG[C/T]GAGACACCATCTAAA | 55833 |
rs185899630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929895 | TGTAATCCCAGCTAC[C/T]AGGGAGGCTGAGGCA | 55833 |
rs185901350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977540 | TCCAGAGTCTTTTAA[C/T]CACAAAAACCAAGTC | 55833 |
rs185920126 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036957 | AAGTAGGTGGGACTA[C/T]AGGCATGTGCCACCA | 55833 |
rs185923820 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028505 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55833 |
rs185934059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014814 | ATTAAGCAAACTTTT[C/T]CCTAAGTAAATTCAA | 55833 |
rs186019800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951819 | TCTTATCAATTCAGT[A/G]GACACACATAGATTT | 55833 |
rs186051357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033159 | ATATTGAAGAAATAT[C/G]TGCATTCCTGTTTGT | 55833 |
rs186055403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018673 | TCGAGACCATCCTGG[A/C]TAACACGGTGAAACC | 55833 |
rs186083816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043395 | TGCTCTCCAACTCCT[A/G]GGCTCAAGTGATTCA | 55833 |
rs186123253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935136 | TACCTGCACTATCTT[G/T]GGTAATCACTGAGCT | 55833 |
rs186137937 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980774 | CAGCCTGGGCAACAT[A/G]GCAAAACCCTCTCTC | 55833 |
rs186152116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017693 | GCAATTCACGAGGCC[A/G]AGGCAGGCAGATCAT | 55833 |
rs186201728 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023343 | TACTTAACCCATATT[C/T]AATGTACATTAATTT | 55833 |
rs186206167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037968 | AAGTTGAAGACCAGC[C/T]TGTGCAATATGATGA | 55833 |
rs186254800 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958651 | GACCTCAGGTGATCC[A/G]CCCACCGCAGCCTCC | 55833 |
rs186278070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003756 | ACAGAGTTTCACTCT[C/T]GTTGCCCAGGCTGGA | 55833 |
rs186283767 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985413 | ACAAATATAGAGAAT[C/T]AACCTAAGTGTTCAT | 55833 |
rs186380523 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936224 | CTGGGCTCAAGCAAT[A/C]CTCCTGCCTTGGCCT | 55833 |
rs186391049 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959712 | TAAAGGAATTTTTTT[A/T]AAAAAAAGGTTCTTC | 55833 |
rs186392532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008112 | TGCACTCCAGCATGG[C/T]GACAGAGTGAGACTC | 55833 |
rs186398105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966916 | TTTAAAAATCAGTGG[A/G]GAAAATTTACATGAG | 55833 |
rs186399092 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989789 | CCTTAAATCTACTTA[C/T]TAATTCAAAGACCAC | 55833 |
rs186453978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004156 | AAGATATATACTCAA[C/T]GAGCAGTAAATAAGA | 55833 |
rs186466180 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921586 | ACCATTTCAAGCCTT[G/T]ATAGCCTGTGTCAGA | 55833 |
rs186470182 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038791 | GCTGCCCAGACTGGG[A/T]AGTGAGGAGCGCCTC | 55833 |
rs186477050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025876 | TGAGCTACCATGCCC[A/G]GTTTAACTGCTGTTT | 55833 |
rs186483191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981749 | GCAAGGAGGGATGGA[A/G]GGATGGAAGGTAGGT | 55833 |
rs186496318 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987240 | ACACACGGAAACCCT[C/G]TCTCTACCAAAAAAT | 55833 |
rs186504952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943888 | CCTGGACAACACGGC[A/G]AGACCCTGTCTCATT | 55833 |
rs186516382 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967638 | GCAAAGCACCACAGG[C/T]AAAGCTGATCAGCCA | 55833 |
rs186548329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948116 | TCATATTTGCATGCT[C/T]TTACCATACTTTTCA | 55833 |
rs186549882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990289 | ACAGAAAAACAAAAT[C/T]TGACATTATATATCC | 55833 |
rs186585002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026725 | ACACTCTAGAGTACA[C/T]ATTACTTTACTCCCA | 55833 |
rs186615282 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005021 | TAATCCCAGCACTTT[C/G]GGAGGCTGAGGCAGG | 55833 |
rs186629031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024125 | GCATTTTGGGAGGCC[A/G]AGCCGGCTGGATCAC | 55833 |
rs186645188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023701 | AATTAAGGTTTACTG[C/T]TCTGGGTTATATATT | 55833 |
rs186768909 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973007 | GAAACCCTGCTCTAA[C/T]GCCTGTTTAAAAGAT | 55833 |
rs186792463 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050748 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 55833 |
rs186814136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008742 | TAGGCTGAGGCAGGC[A/G]GATCACAAGGTCAAG | 55833 |
rs186824477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042362 | GGGCACCTATAATCC[A/G]AGCTACTCGGGAGAT | 55833 |
rs186931898 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012948 | CTGAGGTCAGGAATT[C/T]AAAACTGACTAACCT | 55833 |
rs186935817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942054 | TGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 55833 |
rs186951077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976580 | AAGGTATACTTCTGC[A/G]GTGTGGAAAATGTTC | 55833 |
rs187030653 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028003 | ATGAGATCCAATTCC[A/C/G]TGCAGCTCAACTGCT | 55833 |
rs187045211 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045074 | AAAAAAAGGCTGGGC[A/G]CCGTGGCTCACCCCT | 55833 |
rs187098296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924977 | ATTATTCTTTCAATG[C/T]GGCCCAAGGAAGCCA | 55833 |
rs187126580 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972510 | CACCAAGAGTGCTGC[C/G]TGAAGTTAGAGAGAG | 55833 |
rs187156760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966725 | CTACTAAAAAAAGTA[C/T]TGTTTTTCTTATTCT | 55833 |
rs187178560 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030432 | CCAGCCTGGGCGACA[A/G]AGCCAGATTCCATCT | 55833 |
rs187181534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016119 | ATGATGATGAAGCAG[C/T]AGGGAAGGAGGAGGA | 55833 |
rs187186170 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049621 | GCGGAAGGTGCGCCC[A/G]CTTTTAGTCTTTTTC | 55833 |
rs187233621 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956025 | ACTTTTCCTGAGGCA[A/G]AAGATTTCTGTAATG | 55833 |
rs187246741 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978638 | ACAAAAAATTAGCCC[A/G]ATGTGCTGGCGGGTG | 55833 |
rs187259313 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996902 | GGACAATATAGTGAG[A/G]CCTCATCTTTACAAA | 55833 |
rs187275012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999580 | AATTTTGTTTTTCTA[A/G]GAGACAGGGTTTCAC | 55833 |
rs187279565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946778 | TTGGTATTATAGGCA[C/T]GCACCAAACACACAG | 55833 |
rs187303092 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032340 | CTTGGTCTGTGATAA[A/T]GACTCAGGCATATTT | 55833 |
rs187375501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982502 | ATTTTGACAGTAAAA[C/T]TAAGTGCCCATTTTG | 55833 |
rs187382088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959996 | AGGCTAGAGGGCGGT[C/G]GAATGATAATGCAGC | 55833 |
rs187386790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000164 | TGTCCCCTCAGACTG[C/T]GGTGTAGTGATGCCA | 55833 |
rs187389548 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949464 | CCCCAGCACTTTGGG[A/T]AGCCGAGGTGGGTGG | 55833 |
rs187389691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928350 | TGAACACAGACTATC[C/T]GAATATGGGACAAGT | 55833 |
rs187469245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018120 | TGAGCCCAAGAGTTT[A/G]AGACCAGCCTAGACA | 55833 |
rs187483365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006975 | GTAGACAGAGTACAA[C/G]TGTTTTGCTGTTGAT | 55833 |
rs187488331 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024299 | GTGAGCCAAAATTGC[A/G]CCATTGCACTCCAGC | 55833 |
rs187563371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956589 | CCACCTTGACCTCCC[A/G]AAGTGTTGGGATTAC | 55833 |
rs187571452 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997372 | ACATGTACTAGCTGA[A/C]GTTCAAAACAGCTTG | 55833 |
rs187586308 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039246 | TTGGGGGGCGCCTCC[A/G]CCTGGCCGCCGCCCC | 55833 |
rs187591412 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031104 | GCCAAATGGTAAAAC[C/G]CTCTCTCTACTAAAC | 55833 |
rs187608002 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978353 | CACCCTGGGCAACAG[A/T]GCAAGAGCCCCTTCT | 55833 |
rs187676315 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955551 | ACAAAAAAAAGGGCC[A/G]GGTGTGGTGGCTCAC | 55833 |
rs187682674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931505 | GAGGACAGCTCCACG[A/G]CACTCCTGCTGAGGT | 55833 |
rs187704803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019231 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 55833 |
rs187710498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932404 | AGATGGTGCCCAGGA[A/T]ATCAGAAGCTCGAAC | 55833 |
rs187758859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044273 | AGGCTTGACAGCACA[C/T]GCCTGTAGTCCCAGC | 55833 |
rs187766960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001391 | TTGAAAGAAAACTCA[C/T]TGGAACTACTAAAGC | 55833 |
rs187769096 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963868 | GAGAAGATGGTCACT[G/T]TCAAAGCTATGTATA | 55833 |
rs187769575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938489 | CTTCTCAAAAACTTA[C/T]GTTGAAACAAAAACA | 55833 |
rs187830320 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963466 | GTTCAATTTAACTTG[C/G]TGTTAGTCCTCTAAC | 55833 |
rs187837703 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039009 | CGTCTCTGCCCGGCC[A/G]ACCCGTCTGAGAAGT | 55833 |
rs187839889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978927 | CCAGAAGGAAACCAA[A/C]CCCTGTAACTTCAAG | 55833 |
rs187844680 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939828 | GGGAGGAGGAAGGGG[A/G]GGAGGAGGGGGAGGG | 55833 |
rs187844947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027677 | CCTGGCTAACACGGC[A/G]AAACCCCATCTCTAC | 55833 |
rs187846980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983186 | CCCGGCCCCCCTATA[A/G]TGTGTTTTTATAACA | 55833 |
rs187850997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010914 | GATAAACCAAAGTCA[A/G]GGAGTATGGCTGAAA | 55833 |
rs187972094 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961497 | TTACAGAATACTCAT[A/C]CATAACACATCTAAG | 55833 |
rs187982378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000406 | AAGAAAGTTATTCTT[A/C]TGTGGCGTGACTTTG | 55833 |
rs188005733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033315 | GTCATTTGAAACAAC[A/G]TGGATAGAACCGGAG | 55833 |
rs188034709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932077 | CTGAGCCACACCTCA[A/G]TAACCATAATCTAGG | 55833 |
rs188199479 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025644 | GAGGAAAGAAAGTCT[C/T]CGGCCGAATAAACCA | 55833 |
rs188205572 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041058 | CACATGAGGACAAGT[A/C]AAATTGGTAATCTCA | 55833 |
rs188244062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946533 | GGACAGAGGTTGGCC[C/T]TCTTTTTCTCTATGG | 55833 |
rs188262662 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924340 | CTTGACTCCCAGGAG[A/G]GCAGAACCAGCACAT | 55833 |
rs188264819 | snp | A/C/T | 0.000757569 | 0.0194479 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989031 | TCCACGTCCACGACT[A/C/T]GATTCTTTCTCGCTT | 55833 |
rs188270906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971441 | TCTTAGCTTGCAGAA[C/G]GGAAAATCAAATTCC | 55833 |
rs188325270 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943013 | GCAGCATCATTCACT[A/G]TAGTCAAAAAGAGCA | 55833 |
rs188329516 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993004 | CCAACACAAACAACT[C/T]ACTAAAAAGAGTTAA | 55833 |
rs188361116 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027738 | TGGTGGCGGGTACCT[A/G]TAGCCCCAGCTACTC | 55833 |
rs188382918 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928768 | CAAGGCAAGTCTCAA[A/G]AAAGGGAAGAAAAGC | 55833 |
rs188397249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950959 | CAATCCCAAAGATGA[A/G]GACATGTTTTGTTTT | 55833 |
rs188414268 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975174 | TGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 55833 |
rs188429462 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993595 | GGCATAAGCCCGGGA[A/G]GTCGAGGCTGTAGTA | 55833 |
rs188469195 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937477 | CTAGGTGGGGTGACA[C/G]ACACCTGTAGTTCTA | 55833 |
rs188489714 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015929 | TTGCCTCAGCCTCCC[A/G/T]AAGTGTTGAGATTAC | 55833 |
rs188499667 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | UBAP2 | GRCh38.p7 | 9:33944518 | TGTTGATTCTCGAAG[A/T]TTTGCCTGGGAAGGA | 55833 |
rs188514087 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987725 | TGGACTTGCTGTGAA[A/G]TTTTTGCTTCAAAAA | 55833 |
rs188520108 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34048977 | AGCCACAACACGTCG[C/T]TCGTGCGCGGCTTCA | 55833 |
rs188573399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998543 | ATGTCTGGTTCAATG[C/T]TCACATGTAAACACT | 55833 |
rs188589288 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031918 | AAGGAGGGAGGACTT[C/G]TTGAGCCCAGGAGTT | 55833 |
rs188589471 | snp | A/G/T | 0.000613263 | 0.0175004 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017153 | GAAGTCATCATATAC[A/G/T]GTATATACAAAATAA | 55833 |
rs188622839 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974726 | AGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTC | 55833 |
rs188633236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012463 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 55833 |
rs188641553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044341 | GGGAGGCGGAGTTTG[C/G]AGTGAGCCGAGATAG | 55833 |
rs188753671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944770 | AGGTTTTACACACAC[G/T]ATGTGTAACACTTCA | 55833 |
rs188768044 | snp | C/T | 0.000161503 | 0.00898473 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922822 | AGTGGAGCCCAAGAC[C/T]GAGGGCAGGCTGAAA | 55833 |
rs188775673 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922224 | GATGGGGTGGGGGTG[C/T]TTATTTTGCTACAGT | 55833 |
rs188777683 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969216 | CTATATTTTCCTTTC[C/T]TTTGGGTATGCATCT | 55833 |
rs188795046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030384 | AACCCGGAAGGCGGA[A/G]GTTGCAGTGAGCCGA | 55833 |
rs188796461 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034279 | AAGTTTTTCATTATA[A/G]TTCTTCAACTTTCCT | 55833 |
rs188842196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974034 | AACATAGGGAGACTC[C/T]CTCTCTACAAAACTA | 55833 |
rs188842255 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927621 | AGGCCAGGAATCCTG[C/T]AAGGAAGAATTCATC | 55833 |
rs188846080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035177 | CAAATCTTTCTTCTG[C/T]TCTCATTCTTTCATC | 55833 |
rs188899109 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929910 | TAGGGAGGCTGAGGC[A/C]GGAGAACTGCTTGAA | 55833 |
rs188913484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002275 | CTCTTTTATCAAAAA[C/T]AGAATACTTAACATA | 55833 |
rs188918467 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952610 | CTGATAAACTTTCGC[A/G]TTTAATTGGAAAACA | 55833 |
rs188922651 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984024 | TTCTCGTGCCTCAGC[A/G]TCCCGAGTAGCTGGA | 55833 |
rs188935965 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020761 | GCTTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 55833 |
rs189062583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957503 | TTAAATGAAATCATA[A/T]AAGTATCCAAACCTT | 55833 |
rs189072750 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933169 | CCACCTCAGTGACAT[C/G]GGCCCAGCGATGCCC | 55833 |
rs189074451 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020030 | CCAGGCATGGTGGCA[A/G]ACGCCTGTAATCCCA | 55833 |
rs189078998 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979880 | TCTAAATAAATAAAT[A/C]AGTGTAACCGGTGAA | 55833 |
rs189100712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032040 | GTCCCACCTCCTTGG[A/G]AGGCTGAGGCGGGAG | 55833 |
rs189130081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949142 | ACTGCACTACAGCCT[A/G]GGCGACAGAGCAAGA | 55833 |
rs189138712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992245 | AATACAAAATTAGCC[A/G]GGCGTGGTGGCGCAT | 55833 |
rs189187297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998176 | GGAGGCCAAGGCAGA[C/T]TGCTTGAGCCCAGGA | 55833 |
rs189296725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941112 | TATTGGTACATCTCA[A/G]CTTAACAGAAAGCAA | 55833 |
rs189347026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026209 | TAAAAGTTTGAACAG[C/T]TAATTAAATCCCAAA | 55833 |
rs189355897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041800 | AGGCCGAAGCAGGCA[A/G]ATCACCTGAGGTCAG | 55833 |
rs189490927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985305 | GGTATTTAGGATATC[C/T]GTTACCATGAGCATT | 55833 |
rs189512070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045299 | TGAAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 55833 |
rs189512197 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003589 | TTTTACTATTTTTAG[A/T]ACAGATGCGGTTTCA | 55833 |
rs189589906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934100 | CAATGCTCACGGCCA[A/G]CGTAAGGCAGATTGG | 55833 |
rs189596303 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007397 | GCTACCCGAGAGGCT[A/C/G]AGGCAGAAGGATCTC | 55833 |
rs189597805 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966243 | ACTTGAGGTCAAGAG[C/T]TCAATACTTACCTGC | 55833 |
rs189607126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040288 | GAGCCCACGCCATTG[A/C]ACTCCAGCCTGGGTG | 55833 |
rs189617481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037020 | TTTTGAGAGAGTCTC[A/G]CTCTATCACCCGGGC | 55833 |
rs189617681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022233 | CTGGGCAACAAGAGC[A/G]AGACACCATCTAAAA | 55833 |
rs189619210 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949026 | AAAAAAATTAGCCGG[A/G]AGTTTTGGCAGGCGC | 55833 |
rs189635992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973483 | TGGTATTTGACAGCT[A/G]AACACAGGGAGGTTG | 55833 |
rs189648028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009998 | GTTTAGTAGAGACGG[A/G]GTTTCTCCATCTTGG | 55833 |
rs189651779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991793 | TTAGAATACAAAAAG[C/T]AAATTCCAGAGGTCC | 55833 |
rs189653726 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027586 | AAATAGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 55833 |
rs189670841 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970321 | TCAAATAACAACTTA[C/T]AAATTTTGTTGACCC | 55833 |
rs189716984 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002833 | AGCTGGGAATACAGG[C/T]GCACAACACGACACC | 55833 |
rs189733353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036201 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAA | 55833 |
rs189765723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044126 | AAATTAGCCGGGCGC[A/G]GTGACTCACGCCTGT | 55833 |
rs189848086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988278 | AAGTATCCACTACAT[A/G]GTAGATACTCAATAA | 55833 |
rs189861780 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024747 | TCAGCACTTTGGGAG[G/T]CTGAGGCGGGTGGAT | 55833 |
rs189867587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957712 | TCTAATGAGGTAACA[C/T]GGAAAACATAAAAAT | 55833 |
rs189911451 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028974 | TTTTTTAATTAGCCA[C/T]GCTTGGTGGCGCACA | 55833 |
rs189911605 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048442 | GCGGAAAGGTGATGA[A/C/G]ATGGGACCGACAGCG | 55833 |
rs189959098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964509 | GCTTCAAAGCCATGG[A/C]AGCCAGCACAGCTTC | 55833 |
rs189960359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952919 | CTGTCACCCAGCCTG[A/G]AGTACAGAGGCATGA | 55833 |
rs189976916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995013 | TGTATCCTCTTTTAG[A/G]TGAGTCATTTTTTTT | 55833 |
rs189979063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977407 | GCAAGATAATAGAAT[C/T]ATTGTTTCCTACTCA | 55833 |
rs189995755 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995422 | AAGTATATATATTTA[C/T]ATATTATTAAACAAA | 55833 |
rs189999650 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943121 | ATGATACATTAAACA[A/T]GGGTGTACCTCGAAA | 55833 |
rs189999862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030038 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAAC | 55833 |
rs190005711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014717 | AGAGAATCACTTGAA[C/T]CCGGGAAGTGGAGGT | 55833 |
rs190113801 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926726 | CTGGGAAGCCCAGGT[A/C]CATCTAGGAGTCAAA | 55833 |
rs190124730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946864 | CTAGTTATGTGTGCA[G/T]AAAAAGTTAATATAG | 55833 |
rs190143647 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014495 | TTAACTGGAGGTGGA[G/T]GCAGGCACCTGTAAT | 55833 |
rs190145018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948153 | GTACTACCACCACAA[G/T]TACTACCAACAATAA | 55833 |
rs190152918 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973069 | AAATCTCTTTAAGTA[A/C/T]AGAAAACACTAGATT | 55833 |
rs190172325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045825 | AAAAGGATCCTATTC[C/T]TAAATACTTGATAGT | 55833 |
rs190240394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016876 | ACCTACTGTTTAAAC[A/G]AAGGGTCCAAAATCC | 55833 |
rs190256648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989859 | CAACCTTGCCTGTTC[C/T]ATTATTCAAACTAAT | 55833 |
rs190366213 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925873 | CAACTCTCTGACAAG[C/T]GCCCTGGGAAATGGC | 55833 |
rs190385849 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975624 | TAACACGGTGAAACC[C/T]CATCTCTACTAAAAA | 55833 |
rs190408266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000169 | CCTCAGACTGCGGTG[C/T]AGTGATGCCATCATA | 55833 |
rs190422324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013428 | AGGTGGAGGCAGAGG[G/T]TGCAGTGAGCTGACA | 55833 |
rs190436332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033172 | ATCTGCATTCCTGTT[C/T]GTTGCAGCACTGTTT | 55833 |
rs190466959 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929435 | AATTTTCAAGGCTTC[C/G]CTCAGTCCATCCAAT | 55833 |
rs190488940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972790 | CATTCAAAGACAATG[G/T]CTGGATTAACTAAAA | 55833 |
rs190498810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031170 | GTAATCCTACTACTC[A/G]GGAGGCTGAGGCAGA | 55833 |
rs190519396 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008283 | AGATCGCGCCATTGC[A/C]CTGCAGCGTGGGCAA | 55833 |
rs190554550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955675 | CTACTAAAAATACAA[A/C]ATTAGCTGGGCGTGG | 55833 |
rs190554722 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003803 | TTGGCTACTGCAACC[A/T]CCACTTCCCAGGTTG | 55833 |
rs190563001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023474 | CATAACTCTTTGTTA[A/T]AACGCAAACTATTAA | 55833 |
rs190571773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978460 | ATAGACCGTATTCAT[C/G]CAATAATTAGTTTTA | 55833 |
rs190579170 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016080 | ACACACTTAAATTAA[C/T]AGAAGGGAGAAAAGG | 55833 |
rs190581385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996424 | ACAGAATTACATAAT[C/T]CTTCTACATGAAGAT | 55833 |
rs190647158 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951386 | AGAGTTTCTCTCGTC[A/G]CCCAGGCTGGAGTGC | 55833 |
rs190652747 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994504 | AAAGAGGGCGGTTAG[A/G]CTCTTCAGTTCACTT | 55833 |
rs190666991 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028499 | ATTAGCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 55833 |
rs190686016 | snp | C/T | 0.00107717 | 0.0231824 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998883 | GAAAGTACATACAAT[C/T]GTTAAGGATTTGAAC | 55833 |
rs190696245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927585 | ACAAAGAGGAAAGAC[G/T]GAAAAGCTAGAAGCA | 55833 |
rs190731930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044283 | GCACACGCCTGTAGT[C/G]CCAGCTACTCGGGAG | 55833 |
rs190774529 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958978 | ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA | 55833 |
rs190887557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936959 | AAAAAAAAACAGTCT[G/T]AATAGCCCTCTACCA | 55833 |
rs190898364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959839 | ATATTCTAAAGAATA[A/G]TAGTTCACAAATCTG | 55833 |
rs190911833 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982115 | TTTACAACTCTGAAG[C/T]TAAGCTTCAGGAAAG | 55833 |
rs190927491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018324 | AGCTGTAACACTATA[A/G]TTGTTTTTTTGTTTA | 55833 |
rs190935955 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999890 | TATGTATGTATGTAT[G/T]TATGTATGTATGTAT | 55833 |
rs190943105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980776 | GCCTGGGCAACATGG[C/T]AAAACCCTCTCTCTA | 55833 |
rs190946126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017733 | AGATCGAGACCATGC[G/T]GGCTAACACAATGAA | 55833 |
rs190983088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023900 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCACG | 55833 |
rs191027404 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935211 | CCACAGTGAACATTT[A/C]TCTCTCTTTCTAAGC | 55833 |
rs191041155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941563 | ATTTGTAAAATAAAA[C/T]CATATCCAAGAAGCA | 55833 |
rs191072538 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966621 | TTTTATGAGGGTCTT[A/C]TTTGATCTTTCCCAA | 55833 |
rs191073053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986480 | GCATTGTATTCCAAA[C/T]GTAATACAATTATAA | 55833 |
rs191193403 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939777 | AGGGGGAGGAGGAAG[A/G]GGAGGAGGAAGGGGA | 55833 |
rs191216453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937573 | GATCGCACCACTGCA[C/G]TGGGCGATAGAGCCA | 55833 |
rs191237976 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004753 | AGCGCCACTGCACTC[C/T]AGCCTGGGCAAAAGA | 55833 |
rs191249539 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038792 | CTGCCCAGACTGGGA[A/C]GTGAGGAGCGCCTCT | 55833 |
rs191290391 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930559 | AGTTGAAGGACACTG[C/T]ACATAAAATACTCTC | 55833 |
rs191302736 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966934 | AAATTTACATGAGAC[A/G]GACCACCGTGAATTA | 55833 |
rs191335934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982513 | AAAATTAAGTGCCCA[A/T]TTTGTCGCCCAGATA | 55833 |
rs191344182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008802 | AAACCCCGTCTCTAC[A/T]GAAAAAACAAAAATT | 55833 |
rs191354447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042813 | GCCAGGCATTAAGCT[C/T]ACACCTGTAATCTCA | 55833 |
rs191457283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990720 | GGCTCACTGCAACCT[C/G]CATCTCCTGGGTTCA | 55833 |
rs191481309 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975268 | AACCCCGTCTTTATT[A/T]AAAAAATGCAAAAAT | 55833 |
rs191489079 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966751 | ATTCTTTGTTTGCAA[G/T]TGTTCACTGCTAGTA | 55833 |
rs191495948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993940 | CGCACTGTCGCCTGG[A/G]CTGGAGTGCAATGCC | 55833 |
rs191504081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028309 | AATTGCCCATAGCTG[C/T]TTGCACACATCTGTC | 55833 |
rs191509503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013314 | CAGCACTTTGGGAGG[C/T]GGAGCTGGGTGGATC | 55833 |
rs191513819 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045241 | GTCCCAGGTACTCGG[C/G]AGGCTGAGGCAGGAA | 55833 |
rs191581686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960267 | GTTTGTTTTTTTCCA[A/G]TCTCCCAATCATCTT | 55833 |
rs191594337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027311 | CATAGTGAAACCCTA[A/C]CCTACTAAAAATACA | 55833 |
rs191616356 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978729 | AGCGTGCAATGAGCC[A/G]AGATTGTGCCACTGC | 55833 |
rs191618087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945827 | TTTTATAAAACCAGT[A/G]CTATATTAATGGACT | 55833 |
rs191629465 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923129 | CCTGCCTGAGAGGGG[A/C]TCAGGCAGGAGCCCA | 55833 |
rs191632287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997228 | TTCTCATTAGCAAGA[A/G]ATACTTGTTACTTAG | 55833 |
rs191633149 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030393 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATCGCGCC | 55833 |
rs191638345 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030589 | GATCACGCCAGTGCA[A/C]TCCTAGTACAGTGCC | 55833 |
rs191638473 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988326 | GAGACAGCAAGAGTC[C/T]CAGGGTGATATGTTA | 55833 |
rs191642827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970648 | TATGTTAACCAGGCT[C/T]GTCTCAAACTCTGGC | 55833 |
rs191760244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985468 | GTGATATATTTACAG[A/G]TTGGAATACTACTCA | 55833 |
rs191800334 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020891 | ATGGTCGCGATCTCC[C/T]GACCTCGTGATCCAC | 55833 |
rs191804908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027682 | CTAACACGGCGAAAC[C/T]CCATCTCTACTAAAA | 55833 |
rs191816107 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035553 | AGGTTTGTGGTGGCA[C/T]GTGCCTGTAATTCCA | 55833 |
rs191824349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942555 | CAACATGACGAAACC[C/T]TGTCTCTACAAAACA | 55833 |
rs191925057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928480 | GGATTCTCAGCCACT[A/G]TGGTCTGGAAACAGG | 55833 |
rs191929267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993201 | CTTAACACCTTTTCC[A/G]AGTAATAATTTTGTT | 55833 |
rs191936991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974969 | GGGGCGGGCAATGGA[C/G]TTGAATATGGATTTC | 55833 |
rs191943191 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049047 | CCTCCACCCCAACCC[C/G]GCGAAGCCAACCGCG | 55833 |
rs191999286 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931250 | GGGACTTGAGAATGT[A/G]CAGATTTTGGTGTAT | 55833 |
rs192056946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931625 | TGTGTGTTTTATGAT[A/G]AAAGATTCTGTGTAA | 55833 |
rs192096034 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977907 | GTAGTCCCAGCTTCT[C/T]GGGAGGCTGAGGCAG | 55833 |
rs192097307 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032379 | ATACACTCACACTCC[C/T]TCTGCCCTGAGTCTC | 55833 |
rs192108601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015222 | ATGCTTAATTTTGCA[C/G]CAGGTACTGTGCTTA | 55833 |
rs192119615 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048718 | TGGGCGCCGGGGCAG[C/T]CTGCAGGCGGTGGGG | 55833 |
rs192173329 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039384 | gagaacgggccatga[A/T]gacgatggcggtttt | 55833 |
rs192245889 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928861 | GAAAAGCCAAAGAAC[A/G]GGAAGGGCCCAGGAG | 55833 |
rs192246170 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962310 | CTTTTATACATGATA[A/T]GTAGTAAGAATGGCC | 55833 |
rs192310587 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983361 | TTCAGTCATGAAGAT[C/T]TGACGATTTCTCTAA | 55833 |
rs192313976 | snp | C/G | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939928 | AGGAGAAGAAGAGGA[C/G]AAGGAAGAAGAAGAA | 55833 |
rs192321734 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964335 | TATTCTACAACAAAT[A/C/T]GGTTTTGCTTATCTA | 55833 |
rs192333071 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002027 | AGTGGCACAATCACA[C/G]CTCACCATGGCCTCG | 55833 |
rs192341920 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954652 | AAAGTTCCTAGCCTG[A/T]GTTCCTCTCCCTTAT | 55833 |
rs192343934 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034316 | TCCAGGATATCAAGT[A/C]CTGGTTTTTCTTTTT | 55833 |
rs192344249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020112 | TTGCAGTGAGCCCAC[G/T]GCACTCCAGCTTGGG | 55833 |
rs192378436 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000587 | TCGCTAACCAAGTCT[A/G]TACTAACTCCCAACA | 55833 |
rs192382110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033563 | GGGTAACTATAGTCA[A/G]TAACTTAATTGTATA | 55833 |
rs192456158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995632 | TTATAAATAAATATA[G/T]ACATATGTATAAAAA | 55833 |
rs192494772 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030356 | TGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 55833 |
rs192535412 | snp | C/T | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921633 | GGATCTCCTTTAGCC[C/T]TGTGAAGTCCAGGGC | 55833 |
rs192535781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956462 | TAGCTGGGCCTCCAG[A/G]CACGCACCAGCATGC | 55833 |
rs192612192 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039204 | GTGGGGGGCAGCCCC[C/T]GCCCGGCCAGCCGCC | 55833 |
rs192666169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987329 | AGGCAGGAGAATTGC[C/T]TGGACCCAACAGGCG | 55833 |
rs192666736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951125 | GATCCTCCCATGCCA[A/G]CCTCTCAAGTAGCTG | 55833 |
rs192670678 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944080 | CTGGTCAAGGAACCA[G/T]GCATCCTCCAACTAT | 55833 |
rs192672106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967884 | AAAAAATACTGTGAT[A/T]AACTTGTCTCTTTGA | 55833 |
rs192672654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983050 | ACCCAGCTAATTTTT[C/T]TGTATTTTGAGTAGA | 55833 |
rs192673398 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025075 | AAGACCCTTAAAAAT[G/T]GTTACCACCACTGAA | 55833 |
rs192677887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006280 | GGACTCTAAAAGAAC[A/G]AACATCCACTGGACA | 55833 |
rs192701147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024168 | GTTCAAGACCAGCCC[A/G]ACCATCTCTACTAAA | 55833 |
rs192742871 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019944 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGTTCGA | 55833 |
rs192763690 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044385 | CAGCCTGGGCAAGAG[A/G]GCAAGACTCTGTCTC | 55833 |
rs192799428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012739 | AAGAGAACAGGATAA[A/G]GTAGATGTGACAGAA | 55833 |
rs192837915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007403 | CGAGAGGCTGAGGCA[A/G]AAGGATCTCTTGAGC | 55833 |
rs192853930 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932216 | AGACTCCCTTCTCCA[A/G]CATTGACCTTCTTGC | 55833 |
rs192873385 | snp | A/G | 0.00302762 | 0.0387897 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922467 | TTCTCTCCTGCCCAG[A/G]ATAAGCCTTGCCCCA | 55833 |
rs192873846 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969767 | GCTACTCAGGACACT[A/G]AAGCAAGAGAATCGC | 55833 |
rs192892879 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040496 | CACTCCTACAATCCC[A/G]GCACTTTGTGCGGGT | 55833 |
rs192938063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007132 | AAGAATATAATGTGA[C/T]TTCTTCCTTTGCAAT | 55833 |
rs192964999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002308 | ACCATGTGGAATCAC[G/T]CACAGACACAATTTA | 55833 |
rs192967364 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027779 | GGCAGGAGAATGGTG[C/T]GAACCTGGGAGGCAA | 55833 |
rs193003513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992521 | GCTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 55833 |
rs193051549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949296 | ATGACAAAGATATGC[C/T]TGACCAACAAAAACA | 55833 |
rs193084412 | snp | A/G | 3.29902e-05 | 0.00406128 | missense | UBAP2 | GRCh38.p7 | 9:33944567 | GGAGGAACAGTGACT[A/G]CCTGGCTCTGGTGCT | 55833 |
rs193130348 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050781 | GCGGGCCGATCACGA[A/G]GTCAGGAGATCGAGA | 55833 |
rs193140869 | snp | A/G | 6.71806e-05 | 0.00579532 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932616 | GAGGCTGCTCTGGTG[A/G]CTGGAGAGCGAACTA | 55833 |
rs193161209 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979166 | TTGCTTGAACGTAAG[A/C]GTTGGAGGTTGCAGT | 55833 |
rs193169116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987756 | AACTACTTCCATTAT[A/G]CAACTACGTTAATGT | 55833 |
rs193170810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024458 | TTGTCTTCTGTCAGT[C/T]GTGCCTCTCCACACT | 55833 |
rs193209130 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010998 | AATAATGACCCTAAA[A/G]GCAAGAATATTTAAA | 55833 |
rs193226421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974109 | AGCAGGAGGATCCAT[A/G]AGCCCAGGAGTTGGA | 55833 |
rs193227187 | snp | A/G | 0.00013187 | 0.00811895 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927895 | TTCATGCTACTGGAC[A/G]GGCTGGCGCCTGAGG | 55833 |
rs193283673 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031134 | CATACAAAACTTAGC[C/T]GGGCATGGTGGCACG | 55833 |
rs193298380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956909 | GATTGCTTGAGGCCA[A/G]AAGTAAGGCTTCATC | 55833 |
rs193300840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997647 | AATGCCTGCAACATA[C/T]AATTTTTAAGACACA | 55833 |
rs199527164 | snp | A/T | 0.000417421 | 0.0144408 | missense | UBAP2 | GRCh38.p7 | 9:33944626 | TGGGGATGGCTCAGG[A/T]TGAGATTTGAAGTCT | 55833 |
rs199549189 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955182 | TAAGTTCATTCTGTC[-/A]AAAAAAAAAAAAAAC | 55833 |
rs199556111 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024636 | GGGTCAGAAAATAAC[A/T]TTAACAGGATGCATG | 55833 |
rs199556221 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009257 | GTGCACACCACCACG[A/G]CCAGCTAATTTTTCT | 55833 |
rs199583079 | in-del | -/TAAA | 0.442385 | 0.15965 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995539 | ATATATTTATATTAT[-/TAAA]TAAATATATTATTAA | 55833 |
rs199586045 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923392 | ACCTGTACTGTAGCC[A/G]TGCTGGCCATAACCA | 55833 |
rs199599751 | snp | C/T | 0.00199792 | 0.0315431 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989037 | TCCACGACTCGATTC[C/T]TTCTCGCTTTTCTTC | 55833 |
rs199607241 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000681 | TAATAAACAGCTTTT[-/A]TTCTGAGTTTTTTAT | 55833 |
rs199621223 | snp | A/G | 1.74928e-05 | 0.00295738 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932646 | AGAAGACAAAACAGA[A/G]CGCCGTATGTCCACC | 55833 |
rs199657011 | in-del | -/T/TTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009107 | TGGTGTTTTGTTTTG[-/T/TTTT]TTTTTTTTTTGAGAC | 55833 |
rs199660426 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958418 | TGGTTCCCCACCCCC[C/T]TTTTTTTTTGAGATG | 55833 |
rs199669810 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939066 | AAACATGGAAAGCTC[A/G]CCATTTTACTCAGTT | 55833 |
rs199686348 | snp | A/G | 0.000214135 | 0.0103451 | missense | UBAP2 | GRCh38.p7 | 9:33923904 | AAGGGCTGCTGGGCT[A/G]TGTGGTGGGTCTGTG | 55833 |
rs199717494 | snp | C/G | 8.23866e-05 | 0.00641767 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924009 | ACATCACCTAGGAAA[C/G]AGCACTGACTCCAGC | 55833 |
rs199744917 | in-del | -/T/TT | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003070 | GTTGTTTTTTTTTTT[-/T/TT]CTTTTTTTGAGACGA | 55833 |
rs199757356 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962679 | TAAATAAATAAATAA[-/TT]ATAATTAAAAAATAG | 55833 |
rs199808909 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008642 | GTAAGATATATACTA[A/T]CACTTTACAGAAAAG | 55833 |
rs199823531 | snp | C/T | 0.00345564 | 0.0414232 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986828 | TCAATTCCATTTTCT[C/T]CACCTCTAACTAGGG | 55833 |
rs199831873 | in-del | -/A | 0.272511 | 0.248984 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994668 | CCCAAAAAAAAAAAA[-/A]TCACAAATTTGATGG | 55833 |
rs199847092 | snp | A/C/G | 0.000115321 | 0.00759266 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986784 | GGGCTCGCTTGCCAC[A/C/G]ATCTGAAGGTTTGTC | 55833 |
rs199859255 | snp | A/G | 7.25887e-05 | 0.00602404 | missense | UBAP2 | GRCh38.p7 | 9:33922700 | ACCTGTGCATCCTGC[A/G]GAAGGTGGTGGTGCA | 55833 |
rs199864531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941635 | TCTGAGAAAAAAACT[A/G]AAATACCACTTACCA | 55833 |
rs199923555 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969563 | TTTAAAAAAAAAAAA[-/G]AGAAAGAAAGAAAGA | 55833 |
rs199942982 | snp | C/T | 0.000165036 | 0.00908243 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944358 | GACTTCATGATGAAA[C/T]GCCCACCTTAGAAGC | 55833 |
rs199953053 | in-del | -/TAAA | 0.191147 | 0.242974 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995602 | AAAATTTAAAATTAT[-/TAAA]TAAATATATATTTAT | 55833 |
rs199974798 | in-del | -/AAAAAAAAAAAAAAA | 0.0174175 | 0.0916809 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046644 | ACAAGACTCCATCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 55833 |
rs199980584 | in-del | -/G | 0.0189856 | 0.0955633 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944037 | GACTACTCTATTTTT[-/G]GGGACTCACCAATGA | 55833 |
rs199991569 | snp | A/G | 0.000662087 | 0.0181826 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933525 | GCTGCTAGTCAGGTC[A/G]CCAGTGTGCTGGGAT | 55833 |
rs199992495 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976906 | AATGCCAGCTATTAG[G/T]GAGGCTGAGGCAGGA | 55833 |
rs200001967 | in-del | -/TAAT | 0.0267878 | 0.112589 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048065 | AGATGCGTGGGCAAC[-/TAAT]TAGACTAAAAACTCA | 55833 |
rs200005428 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044285 | ACACGCCTGTAGTCC[A/C]AGCTACTCGGGAGGC | 55833 |
rs200019094 | in-del | -/AAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018863 | CAAGACTCCGTCTCA[-/AAAT]AAATAAATAAATAAA | 55833 |
rs200020259 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975445 | TTTAAAAAAAAAAAA[-/C]AAAAAAAAAACCAAG | 55833 |
rs200097712 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943915 | ATTTAAAAAAAAAAA[-/A]GGAGAAATTAAAAGT | 55833 |
rs200109018 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947825 | GCAAGATCCTGACTC[-/AAA]AAAAAAAAAAATAAA | 55833 |
rs200113756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948599 | ATGACTTTAAAAGGG[A/G]GATAAAAGAACAAAT | 55833 |
rs200124506 | snp | A/G/T | 0.000757588 | 0.0194483 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989030 | TTCCACGTCCACGAC[A/G/T]CGATTCTTTCTCGCT | 55833 |
rs200157072 | snp | C/T | 0.000554934 | 0.0166481 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926975 | GCAGGCCAGGAGTTC[C/T]GCCATACACTCACCG | 55833 |
rs200160464 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006083 | TAAAAATACAAAAAA[-/A]TTAGCCGGGCATGGT | 55833 |
rs200163142 | snp | A/G | 6.59e-05 | 0.00573983 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923888 | CAGTGCAGGATTCAC[A/G]AAGGGCTGCTGGGCT | 55833 |
rs200173680 | snp | A/G/T | 0.000230599 | 0.0107357 | missense | UBAP2 | GRCh38.p7 | 9:33923251 | GCATAGCCACCTTTG[A/G/T]AGTAGTCTCCTGCTG | 55833 |
rs200184963 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33924243 | GCTCCCATCTCGGCT[A/G]GCAAGCGCTGTGGGT | 55833 |
rs200191509 | in-del | -/TA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977044 | TGTTTTTTATTTATT[-/TA]TTTTTTTTTTTTGAG | 55833 |
rs200197460 | snp | C/T | 0.000115311 | 0.00759224 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973209 | GGTTGAGAACCTTCC[C/T]GCCCCTCTCCCTCTG | 55833 |
rs200213100 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996742 | AAATCCAATACAAAT[G/T]TTTTGTCAGGGACAA | 55833 |
rs200217466 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982894 | TGTTTTTTTTTTTTT[G/T]TTTTTGAGACAGAGT | 55833 |
rs200223182 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33971721 | ACACACATCTGTAGA[C/T]GTAGAATCTGAATAG | 55833 |
rs200223875 | in-del | -/T | 0.046775 | 0.145601 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984507 | TCTCTTAAAAAAAAA[-/T]ATTTTTTTTTTTCTT | 55833 |
rs200263850 | snp | G/T | 0.00785611 | 0.0621799 | missense | UBAP2 | GRCh38.p7 | 9:33944423 | TTGGGCTGTGGCTGG[G/T]GGACAGACACAGAGA | 55833 |
rs200263941 | in-del | -/A | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975642 | CTCTACTAAAAATAC[-/A]AAAAAAAAGAAAAAT | 55833 |
rs200269725 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949195 | ATAAATAAATAAAAA[A/T]AAAATAAAATAATAA | 55833 |
rs200274696 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993055 | GATACTTCAAAACAA[-/TT]TTGTCACATCAACCA | 55833 |
rs200313437 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040718 | TGTTGGCAAGGATGT[A/G]GAACTCTTAAACCAC | 55833 |
rs200317929 | snp | C/T | 0.000399281 | 0.0141238 | missense | UBAP2 | GRCh38.p7 | 9:33944570 | GGAACAGTGACTGCC[C/T]GGCTCTGGTGCTGTT | 55833 |
rs200331065 | snp | G/T | 0.000872895 | 0.0208731 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33956098 | GCCCAGGTAAGATGT[G/T]ATTCTCTGCTGGAGC | 55833 |
rs200335055 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956943 | AGGAAAAAAAAAAAA[A/T]TTGGCTGGTCGTGGT | 55833 |
rs200343274 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942742 | CAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAC | 55833 |
rs200361280 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007648 | GTATGTTTTATTTTT[-/A]TTTTTTTTGAGACTG | 55833 |
rs200368695 | snp | A/G | 1.65919e-05 | 0.00288022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932545 | GCGGAGGAAGAGGAA[A/G]CCGCGCAGACACTTA | 55833 |
rs200377125 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978037 | AAAAAAAAAAAAAAA[C/T]ACTGATCTGTAATCC | 55833 |
rs200381237 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971856 | AAGCCCAGTGCCTTC[C/T]CACAGCCACTGTAAA | 55833 |
rs200416980 | in-del | -/A | 0.0872718 | 0.189788 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966049 | GCGAGACTCCATCTC[-/A]AAAAAAATAAAAAAT | 55833 |
rs200473620 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963987 | GATGGCTCTTGGACA[G/T]TCAAATCACTTCAAT | 55833 |
rs200565899 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933292 | TGCCAGCAGAGGCGG[A/C]ACAAGCAGGCAAGGT | 55833 |
rs200578214 | snp | C/G | 4.94295e-05 | 0.00497115 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33956115 | TTCTCTGCTGGAGCA[C/G]ATGAGGCAGTGAAGA | 55833 |
rs200579105 | in-del | -/AAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034888 | ACAAACAAACAAACA[-/AAC]AAAAAAAAACGAATC | 55833 |
rs200579962 | in-del | -/AAAAAAAAAA | 0.387263 | 0.208947 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930896 | GTGAGACTGCATCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAGC | 55833 |
rs200580186 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004798 | CCAAAAAAAAAAATA[-/G]GGAAAAAAAAAGTAA | 55833 |
rs200586711 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938796 | GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs200592930 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018230 | GGATAGCGATTACAA[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs200594160 | snp | A/G | 0.000164715 | 0.0090736 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944422 | TTTGGGCTGTGGCTG[A/G]TGGACAGACACAGAG | 55833 |
rs200615154 | snp | A/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024637 | GGTCAGAAAATAACT[A/G/T]TAACAGGATGCATGA | 55833 |
rs200624840 | snp | C/T | 1.64923e-05 | 0.00287156 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923780 | AGACACAGTCACACC[C/T]TCTGAAATACTCACA | 55833 |
rs200638782 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962676 | TAAATAAATAAATAA[A/T]TAAATAATTAAAAAA | 55833 |
rs200641582 | snp | G/T | 4.94287e-05 | 0.00497111 | missense | UBAP2 | GRCh38.p7 | 9:33948443 | TAGTAGTTGTAGGGT[G/T]ACTTGTACTATTCTG | 55833 |
rs200658681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937839 | AGGCAGGAGAATCAC[A/G]TGAACCCAGGAGGCA | 55833 |
rs200660358 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003071 | GTTGTTTTTTTTTTT[C/T]TTTTTTTGAGACGAA | 55833 |
rs200722543 | in-del | -/A | 0.0065301 | 0.0567662 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017007 | GTATAATAATAAAAG[-/A]AAAAAAAAGGAAAAA | 55833 |
rs200757378 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941874 | CTCACTGAAAAGAGT[A/C]AAAAATATTCAACAT | 55833 |
rs200778832 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040197 | GGTGTGGTGGCACGT[A/G]CCTGTAGTCCCAGCT | 55833 |
rs200784786 | snp | A/C/G | 0.000646556 | 0.0179687 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935802 | CTCTGTTTGGTTGGC[A/C/G]CCAGCCATGACAAGA | 55833 |
rs200803621 | in-del | -/AGGAAGAGGAGGAATAGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016178 | AGGAGGAGGAGGAGG[-/AGGAAGAGGAGGAATAGA]AGGAAGAGGAGGAAT | 55833 |
rs200858756 | snp | A/C/G | 0.00598202 | 0.054362 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922399 | GAGGCATGGCTGACA[A/C/G]ATGTCGGGAATTCTA | 55833 |
rs200871930 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939947 | GAAGAAGAAGAAAGA[C/G/T]GGAAGGAAGGAAGAA | 55833 |
rs200887283 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975446 | TTAAAAAAAAAAAAC[-/AAAA]AAAAAACCAAGTGTT | 55833 |
rs200916448 | snp | A/G | 3.30235e-05 | 0.00406333 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998828 | AATCATTCTTATCAA[A/G]GATCACTTGAGCGAG | 55833 |
rs200919379 | snp | C/T | 0.000518167 | 0.0160877 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922643 | AAGGCTGGAGCAGAA[C/T]CCCTGGCCCAGAGTA | 55833 |
rs200920721 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019938 | AGGCTGAGGCAGGCA[C/G]ATCACGAGGTCAGGA | 55833 |
rs200928238 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945512 | CAAACAAACAAAAAA[G/T]AAAATCCAATAGATA | 55833 |
rs200946007 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33988973 | AAAGTCTGTACTTAC[A/C]TTCTCTGCCACGATT | 55833 |
rs200986225 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969565 | TTAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 55833 |
rs201000373 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941901 | ACATAATTTTGTTAC[C/T]TTAAATAGCTTCATA | 55833 |
rs201007873 | in-del | -/G | 0.0283406 | 0.115616 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939959 | GAGGGAAGGAAGGAA[-/G]GAAGAAGAAAAAATA | 55833 |
rs201029416 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003072 | TTGTTTTTTTTTTTC[C/T]TTTTTTGAGACGAAG | 55833 |
rs201060540 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937132 | GACTGGTGGTGATTC[-/A]AAAAAAAAAAAAAAG | 55833 |
rs201063799 | snp | C/T | 3.29717e-05 | 0.00406015 | missense | UBAP2 | GRCh38.p7 | 9:33944541 | GGGAAGGAAAGGACT[C/T]CAAACCAGGAGGAGG | 55833 |
rs201069752 | in-del | -/AGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016306 | AGGAAGAGGAGGAAG[-/AGA]AGGAGGAAGAGAAGG | 55833 |
rs201071875 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021649 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGGCTC | 55833 |
rs201080426 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954784 | TCTCAAAACAATATA[-/C]TATAAGACATAATCA | 55833 |
rs201091483 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988654 | TAACAGAAGGGAGTC[-/A]ATCACACTACACAAC | 55833 |
rs201096604 | in-del | -/AGGTAGGA | 0.187685 | 0.242109 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981769 | GGAAGGTAGGTAGGT[-/AGGTAGGA]AGGTAGGAAGGAAGG | 55833 |
rs201152194 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969567 | AAAAAAAAAAAAAGA[A/G]AGAAAGAAAGAAAAG | 55833 |
rs201167519 | snp | A/G | 0.000214177 | 0.0103461 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935812 | TTGGCACCAGCCATG[A/G]CAAGAGTAGCTTGCT | 55833 |
rs201178650 | snp | A/G | 0.000955094 | 0.021832 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923193 | AACACTACCTTTGCC[A/G]GGCCCAGAACCTGCA | 55833 |
rs201207838 | snp | A/G | 0.00120251 | 0.024491 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924175 | CGCTAGGCCGGCCCC[A/G]GGCTACTCCTCATCC | 55833 |
rs201229414 | snp | A/G | 0.000280433 | 0.011838 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953437 | CTGAGGCTTGACTGT[A/G]AGGAACAGGCTTCTG | 55833 |
rs201230777 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964714 | AGACCCCCATCTCTT[-/A]AAAAAAAAAGAAGCA | 55833 |
rs201242662 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937131 | AGACTGGTGGTGATT[A/C]AAAAAAAAAAAAAAA | 55833 |
rs201256329 | in-del | -/AAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969563 | CTTTAAAAAAAAAAA[-/AAG]AAAGAAAGAAAGAAA | 55833 |
rs201283769 | snp | A/G | 0.00041175 | 0.0143424 | missense | UBAP2 | GRCh38.p7 | 9:33944447 | ACAGAGATATTTTCA[A/G]TGGTCGTGCTGGGAA | 55833 |
rs201311859 | snp | A/T | 0.00042888 | 0.0146375 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956036 | GGCAAAAGATTTCTG[A/T]AATGCTTTGAATAAC | 55833 |
rs201313370 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029526 | AGAGCAAAACTTCTC[-/A]AAAAAAAAAAAAGAA | 55833 |
rs201318280 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048276 | GAACGGCGGGTGTGG[C/T]GGAAAACTGAGTCCC | 55833 |
rs201323209 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989740 | ATTTCCCCAAGCTCC[C/T]ATTCTACACCACCTC | 55833 |
rs201348462 | snp | C/T | 0.000132013 | 0.00812337 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986853 | CTAGGGGGAAAAGAG[C/T]AGAAAAATCAAATTT | 55833 |
rs201349651 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935691 | TAACACCACAGCCAA[C/T]ACCTGGTCCAAAAAC | 55833 |
rs201362659 | snp | A/C | 0.000938511 | 0.021642 | missense | UBAP2 | GRCh38.p7 | 9:33923245 | GATCCAGCATAGCCA[A/C]CTTTGGAGTAGTCTC | 55833 |
rs201364009 | snp | C/T | | | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989062 | TTCTTCTCTCTATTC[C/T]CTTTGTTTTCTGAAT | 55833 |
rs201370484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923523 | GTAGGAAGAGGCAAG[C/G]TGAGGCTGGTCAGGT | 55833 |
rs201372104 | snp | A/G | 6.96149e-05 | 0.00589937 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922617 | GAGGAAGAGGAGAAG[A/G]GAAGGCTGTCAAGGC | 55833 |
rs201395688 | snp | C/T | 0.000692338 | 0.0185927 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963770 | AGATCCTGAGCTATG[C/T]TGTGAGTATTTGATG | 55833 |
rs201452836 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009807 | ATGACTTATATTTCC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs201457619 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995494 | TATTTATATTATTAA[-/AT]ATATATATATTTATA | 55833 |
rs201466067 | in-del | -/TAT | 0.145978 | 0.227331 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995438 | ATATTATTAAACAAA[-/TAT]TATAAATATTATATA | 55833 |
rs201469863 | snp | A/G | 3.31862e-05 | 0.00407333 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971606 | ATACAACTCTTAATA[A/G]CTCAAACATTTAAAA | 55833 |
rs201516750 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999336 | ATTAAAAAAAAAAAA[-/A]GGCTTAAAAAGTAAT | 55833 |
rs201536475 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993896 | GTTCAGCTTTGCTTT[C/T]TTTTTTTTTTTTTTT | 55833 |
rs201538101 | snp | C/T | 3.30017e-05 | 0.00406199 | missense | UBAP2 | GRCh38.p7 | 9:33927856 | CTCGCGGGGGTCCCA[C/T]CCAGACAGAGGCTGT | 55833 |
rs201592596 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014791 | AAAAAAAAAAAAAAA[C/T]ACCATTCATTAAGCA | 55833 |
rs201610629 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975442 | TCTTTAAAAAAAAAA[-/C]AACAAAAAAAAAACC | 55833 |
rs201632780 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972800 | AATGGCTGGATTAAC[-/T]TAAAATGGCTCTTAG | 55833 |
rs201644643 | snp | C/T | 8.81718e-05 | 0.00663913 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933463 | CCCCAAGGTACTTCT[C/T]ACTTTGGGCCCACAC | 55833 |
rs201650799 | in-del | -/GCA | 0.454182 | 0.144256 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016363 | GAGGCAGCAGCGGCG[-/GCA]GCGGCGGTGGTGGTG | 55833 |
rs201681879 | snp | A/G | 3.33289e-05 | 0.00408207 | missense, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33963730 | AGTATTCATACCTTT[A/G]AGTCCATAAGAACTT | 55833 |
rs201710108 | in-del | -/TGTTT | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009096 | TCCCTAAAAATTTGG[-/TGTTT]TGTTTTGTTTTTTTT | 55833 |
rs201712574 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977045 | GTTTTTTATTTATTT[-/A]TTTTTTTTTTTGAGA | 55833 |
rs201726243 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023235 | AAAAAAAAAAAAAAA[C/T]AAAGAAAATAATCTA | 55833 |
rs201752397 | snp | A/G | 0.000141141 | 0.00839943 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948334 | GCCAAAGCTTGAAAC[A/G]TCCTCAGTAGGGGCA | 55833 |
rs201760141 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941893 | AATATTCAACATAAT[G/T]TTGTTACTTTAAATA | 55833 |
rs201788740 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931695 | TAGCCAGATCCAGAG[A/G]AAAGGACAGGATGTC | 55833 |
rs201828845 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993051 | GACCGATACTTCAAA[-/A]CAATTTTGTCACATC | 55833 |
rs201830433 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929589 | TACACAGATCTATGT[-/A]AAAAAAAAATCATAA | 55833 |
rs201839050 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965257 | CTAGAACTTCTTCCA[-/T]TTTTTCCCCCCATTT | 55833 |
rs201910117 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931622 | GTTTGTGTGTTTTAT[A/C]ATAAAAGATTCTGTG | 55833 |
rs201917526 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001977 | ATTAAAAAAAAAAAA[-/A]CAAAAAAACAGGGTT | 55833 |
rs201922568 | snp | A/G | | | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989027 | TGTTTCCACGTCCAC[A/G]ACTCGATTCTTTCTC | 55833 |
rs201943009 | in-del | -/G | 0.0869089 | 0.189476 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949141 | ACTGCACTACAGCCT[-/G]GGGCGACAGAGCAAG | 55833 |
rs201968722 | snp | C/G | 0.000881128 | 0.0209711 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922500 | CCACCCCTCTCTTCT[C/G]GGTTTAGTTTGTCCA | 55833 |
rs201982649 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924160 | AGCTCCTGGAGTTCG[C/T]GCTAGGCCGGCCCCG | 55833 |
rs202041719 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044264 | AAATTAGCCAGGCTT[A/G]ACAGCACACGCCTGT | 55833 |
rs202041904 | in-del | -/AG | 0.0883596 | 0.190715 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939944 | AAGGAAGAAGAAGAA[-/AG]AGGGAAGGAAGGAAG | 55833 |
rs202084459 | snp | C/T | 0.00028005 | 0.0118299 | missense | UBAP2 | GRCh38.p7 | 9:33944384 | GAAGCTGGGGGTATC[C/T]GCCGCTTAGCAAGTT | 55833 |
rs202086295 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981523 | AATTTTTTTTTTTTT[-/T]AAACAAAAAAAGCCT | 55833 |
rs202098446 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991919 | GGGGCCAGCTGTCTT[C/T]GTAAAACATCTGAGA | 55833 |
rs202125455 | in-del | -/AGGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981777 | GGTAGGTAGGTAGGA[-/AGGT]AGGAAGGAAGGAAGG | 55833 |
rs202135177 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999906 | TATGTATGTATGTAT[G/T]TTATTTTGAGATGGA | 55833 |
rs202162819 | in-del | -/G | 0.195526 | 0.243993 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038140 | ACTGCACTCCAGCCT[-/G]GGGAAAAAAAAAAAA | 55833 |
rs202180819 | in-del | -/TA | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000680 | CTAATAAACAGCTTT[-/TA]TTCTGAGTTTTTTAT | 55833 |
rs202185076 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | UBAP2 | GRCh38.p7 | 9:33923887 | GCAGTGCAGGATTCA[C/T]GAAGGGCTGCTGGGC | 55833 |
rs202188078 | snp | A/G | 0.000362349 | 0.0134552 | missense | UBAP2 | GRCh38.p7 | 9:33944453 | ATATTTTCAATGGTC[A/G]TGCTGGGAAGCTGCA | 55833 |
rs202190453 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969879 | CACCCCCCCACCCCC[-/A]AAAAAAAACCAGTTA | 55833 |
rs202245347 | snp | C/T | 1.73447e-05 | 0.00294483 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927804 | GCAAATACCTGAGGT[C/T]ACCAAGGGCGCGGCC | 55833 |
rs367558768 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031499 | TTTTAGTAGAGACAG[A/G]TTTCGACATGTTGGC | 55833 |
rs367625420 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989203 | CATGCATGTATCTTT[-/C]TTTTTTTTTTTTTTT | 55833 |
rs367630242 | snp | A/G | 1.65151e-05 | 0.00287355 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923764 | GCAACCCAAGGCCAG[A/G]AGACACAGTCACACC | 55833 |
rs367647569 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047389 | GTGTATTGAAGGAAA[C/G]TATCATCTCCAGGGA | 55833 |
rs367667110 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973330 | TCACTACCCAGACAA[C/T]ATTATCATTATTCCT | 55833 |
rs367672869 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990368 | AGTTGAATTATTTCC[A/G]TAACAGTGGAAGCCA | 55833 |
rs367703046 | snp | A/G | 1.64857e-05 | 0.00287099 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924159 | CAGCTCCTGGAGTTC[A/G]CGCTAGGCCGGCCCC | 55833 |
rs367727616 | snp | G/T | 3.29473e-05 | 0.00405864 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948552 | TGCCATTTTTGGTGG[G/T]GCAAGCTCTCCAAAT | 55833 |
rs367758220 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932648 | AAGACAAAACAGAGC[A/G]CCGTATGTCCACCTG | 55833 |
rs367817603 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036590 | GTCTGCTCACCAACA[C/T]GTAAGCAACTGAAGA | 55833 |
rs367901070 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944935 | TAGCTAACAGAGAAT[A/C]ATACTTTTATTATTT | 55833 |
rs367934352 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025821 | CTGGGCTCAGGTGAT[C/G]CTCCCACCTTGGCCT | 55833 |
rs367934629 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989879 | TTCAAACTAATTATC[C/T]AAAACAATTTAATGG | 55833 |
rs367970717 | snp | G/T | 1.64792e-05 | 0.00287042 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924023 | AGAGCACTGACTCCA[G/T]CCACTGCCCTTCCTC | 55833 |
rs367976778 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948495 | AAACTGGCCCAAACT[C/T]GGAGCTTTCAACTGG | 55833 |
rs367981723 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012306 | GAGGTCAAGGCAGGC[A/G]GATCACCTAAGGTCA | 55833 |
rs368021223 | in-del | -/AT/TAATTAATTAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962680 | AAATAAATAAATAAA[-/AT/TAATTAATTAAT]TAATTAAAAAATAGG | 55833 |
rs368048375 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050650 | GGCGGATCACAAGAT[A/C]CGGAGTTTGAGACCA | 55833 |
rs368053740 | in-del | -/TCC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931967 | CCTCTACAATCCTCC[-/TCC]CTCCTCTCCATCTCA | 55833 |
rs368079033 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985183 | GCTGTGGCAATTTCT[A/T]TTTTTTTTTAATTTT | 55833 |
rs368081369 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023008 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATGG | 55833 |
rs368081644 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976561 | TGGTGAAATGATAAA[C/G]GGTAAGGTATACTTC | 55833 |
rs368095174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025646 | GGAAAGAAAGTCTCC[A/G]GCCGAATAAACCAAC | 55833 |
rs368107713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950921 | CATGCACATACACAC[A/G]AACACACACAGTGCC | 55833 |
rs368110650 | snp | C/T | 8.92244e-05 | 0.00667864 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922846 | GCTGAAAGGTGGAGG[C/T]GTCCCTGCATGAAAT | 55833 |
rs368139124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004716 | GTGAACCTGGCAGGC[A/G]GAGCTTGCAGTGAGC | 55833 |
rs368152095 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931364 | ATGGGACCCACTGGA[G/T]GAGACGATTCTGGCT | 55833 |
rs368180112 | snp | A/C/T | 3.30471e-05 | 0.00406481 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926677 | GATCTGTGTGAGAAC[A/C/T]AGAAAGTGTATTTTA | 55833 |
rs368268801 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986891 | CAAACCTCTTGTACA[G/T]AACCTTATCAAGCAC | 55833 |
rs368284092 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035320 | CCAGCCTGGCCAACA[A/T]GGTGGAACCCCATCT | 55833 |
rs368288644 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022695 | CCACCAGCCTCAGCC[G/T]CCAAAGTGCTGGGAT | 55833 |
rs368328902 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950373 | ACCGTGCCTGGCCCA[A/G]AAATAACATTTCATA | 55833 |
rs368368993 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978016 | GAGACTCTGTCTTTT[-/A]AAAAAAAAAAAAAAA | 55833 |
rs368379430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996861 | GCAGAGACGAGAGGA[C/T]TGCTTGAGCCCAGGA | 55833 |
rs368386117 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986482 | ATTGTATTCCAAACG[G/T]AATACAATTATAATT | 55833 |
rs368390826 | snp | C/G | 1.64939e-05 | 0.0028717 | missense | UBAP2 | GRCh38.p7 | 9:33926625 | CACTCACCACTGGCA[C/G]CCGTGACTGCAGCAT | 55833 |
rs368406110 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995678 | ATAAATATATACACA[C/T]AGCAAAATTTTAGGG | 55833 |
rs368448414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032560 | GCTTTCTTAGGGATA[C/T]AAGTTCAATAAAACA | 55833 |
rs368471000 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008636 | CAAAGCGTAAGATAT[A/T]TACTAACACTTTACA | 55833 |
rs368481311 | snp | G/T | 1.64784e-05 | 0.00287035 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986713 | ACGCAACTGCCTGCT[G/T]CTTCCCCCTAATTGA | 55833 |
rs368483440 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047049 | GGAAACAGGCAAGAG[A/C]GGCAATTACCACAAC | 55833 |
rs368536397 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959022 | GGCATGGTGGCGTGC[A/G]TCTATAATTCCAGCT | 55833 |
rs368544303 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039042 | GGAGCCCCTCCGCCC[A/G]GCAGCCGCCCCGTCT | 55833 |
rs368563844 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991368 | AAAATGATCAACAGC[A/G]TAAAAGGAGGGGAGG | 55833 |
rs368571008 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009865 | CAGGCTGGAGTACAA[C/T]GGTGGGATCTCTGCT | 55833 |
rs368580806 | snp | A/G | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986769 | GCTTACCTCTACCCC[A/G]GGCTCGCTTGCCACG | 55833 |
rs368591967 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973623 | GCTGAAGGCACTGTT[A/C]AGTATCATTTTAAAT | 55833 |
rs368603824 | snp | C/T | 4.94434e-05 | 0.00497184 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935786 | GTGAGCTATCCTCTT[C/T]CTCTGTTTGGTTGGC | 55833 |
rs368680658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986589 | TGGTTTCTTCAAAAC[G/T]ACATAACCCAAAATA | 55833 |
rs368688494 | in-del | -/CA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006320 | AAATGTCAAGAGACA[-/CA]GAAGAGAATGAAATT | 55833 |
rs368771067 | snp | C/T | 0.000164723 | 0.00907383 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944452 | GATATTTTCAATGGT[C/T]GTGCTGGGAAGCTGC | 55833 |
rs368852145 | snp | C/G/T | 0.000148457 | 0.00861454 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923481 | AGGCTGGAGGGACCT[C/G/T]GGGGGGCAAGCAGAT | 55833 |
rs368871679 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019504 | ATGGTAGTTACCAGA[A/G]GCTGGGGGTAGGGGA | 55833 |
rs368876152 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992775 | AAGTATACACACATG[A/C]ATACTTTAAAAAGTT | 55833 |
rs368883130 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020827 | ACCAAGCCCAGCTAA[-/T]TTTTTTTGTATTTTT | 55833 |
rs368883735 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010551 | AGCATTAAAAACTTA[C/G]ATAAAATAATGGCTG | 55833 |
rs368895675 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956155 | CAGAAAGCTGTATGG[A/G]AAGTTGAAAAATTTA | 55833 |
rs368897149 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046718 | TCAAGAAAGGTTTGT[A/G]CTTTCTACACATATT | 55833 |
rs368898095 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040471 | TAGTTAAAGAGGTTA[A/G]CTGATGGCTCACTCC | 55833 |
rs368901976 | in-del | -/CTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950067 | AATAACATTTCTTTT[-/CTT]TTCTTTTTTCTTTTT | 55833 |
rs368903814 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956977 | GTGCACCTGTCCCAG[C/T]TACATGGGAGGCTGA | 55833 |
rs368904262 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017000 | AACTTCAAGTATAAT[A/T]ATAAAAGAAAAAAAA | 55833 |
rs368962515 | snp | A/G/T | 4.94507e-05 | 0.00497221 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935896 | ATAAGGAAAAGAAGA[A/G/T]AAGAGAATATAAACT | 55833 |
rs368965909 | in-del | -/ACAC/ACACACACAC/ACACACACACAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954267 | TTTAAGTGTGTGTAT[-/ACAC/ACACACACAC/ACACACACACAC]ATACACACACACACA | 55833 |
rs368978844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945609 | GCAAACACTGTACCC[A/G]GTTTTCCTGAATGTC | 55833 |
rs368989536 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007096 | TTAGGTTTTTCTAAA[C/T]ACAACATGTCATCTA | 55833 |
rs368994955 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024573 | GAAACAGGTTTCGCA[A/C]AACAATCACAGGGGA | 55833 |
rs369053609 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014734 | CGGGAAGTGGAGGTT[G/T]GAGTGAGCCGAGACT | 55833 |
rs369075585 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030587 | GTGATCACGCCAGTG[A/C]ACTCCTAGTACAGTG | 55833 |
rs369094632 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010459 | AAAAAAGACAATAAA[A/C]AAATAATACACCCTA | 55833 |
rs369119407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928737 | AGCAGGTAGGTGGGG[A/G]GCACACCTAGGTGGA | 55833 |
rs369134281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998092 | TATACTTTTCCAACA[A/G]GAGTATGAAATCACA | 55833 |
rs369236024 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029976 | TGGGTGACAGAGCAA[A/G]ACTCCATCTCGAAAA | 55833 |
rs369247749 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030246 | GTCAGGAGATCGAGA[C/T]CACCCTGGCTAACAC | 55833 |
rs369248975 | snp | A/T | 1.75121e-05 | 0.00295901 | missense | UBAP2 | GRCh38.p7 | 9:33922532 | TATGGAGAGTTGCCG[A/T]AGGCAGGTTTGGAGG | 55833 |
rs369280564 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997242 | AGATACTTGTTACTT[A/C]GCATTTTCATCACTA | 55833 |
rs369306917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942502 | GGAGGCTGATGCAGG[C/G]AGATTCATTGAGCTC | 55833 |
rs369318868 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006191 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCCAGC | 55833 |
rs369319014 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936197 | CATGTTGACCAGGCT[C/G]GTCTCCAACTCCTGG | 55833 |
rs369325962 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037582 | AGCCCCAAAAAGTTA[C/T]ATTTTATCCTACAAT | 55833 |
rs369346195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017881 | GCAGTCAGCCGAGAT[C/T]GCGTCACTGTACTCC | 55833 |
rs369356751 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923180 | GAAAGGAGAGGTAAA[C/G]ACTACCTTTGCCAGG | 55833 |
rs369361858 | in-del | A/TT | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921848 | ATAACTCAGATTATT[A/TT]TTTTTTTTTCATGGT | 55833 |
rs369362609 | snp | A/G/T | 3.30334e-05 | 0.00406397 | synonymous-codon, stop-gained | UBAP2 | GRCh38.p7 | 9:33944589 | TCTGGTGCTGTTGTC[A/G/T]CTGGCTCAACTGGCT | 55833 |
rs369367433 | snp | C/T | 0.000331296 | 0.0128662 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996205 | TGTAAACAATGCAAA[C/T]CAATTAATAATACTT | 55833 |
rs369416618 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951421 | GCATGATCACGGCTC[A/G]CTGCAACCTCCACCT | 55833 |
rs369423712 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929781 | CCGAGGCAGGTGGAT[C/G]ACCTGAGATCAGGAG | 55833 |
rs369436264 | snp | A/G | 3.3484e-05 | 0.00409156 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926983 | GGAGTTCCGCCATAC[A/G]CTCACCGGGTAGGCA | 55833 |
rs369455022 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044028 | CCCAGTAGGCGGAGA[C/T]TGCAGTGAACAGAGA | 55833 |
rs369471623 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988035 | TCAGAGGCTGACTCA[C/T]ATGAATTCCAGTGAG | 55833 |
rs369474637 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037091 | ACTTCTGGGATCAAG[C/T]GATTCTCCTGCCTCG | 55833 |
rs369523851 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023607 | AATGACCCGGTTGCA[C/T]GGCTAAACCAGAATA | 55833 |
rs369533673 | in-del | -/ACACAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019689 | TATGTACATTTTACT[-/ACACAC]ACACACACACACACA | 55833 |
rs369603396 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923310 | TAGCGTGGCAGGGTA[C/T]AAGAGGCAAGTGTGA | 55833 |
rs369625432 | snp | C/T | 0.000906417 | 0.0212694 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944674 | ATTAATGAGGCATAA[C/T]GGCTTCACAATGTTC | 55833 |
rs369678183 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048810 | AGGGAAGGAGAGGGA[C/G]AGGATGGCAATTACC | 55833 |
rs369714092 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003363 | CCAAATCTGTACATA[C/T]ATCAAAGATGGCTTT | 55833 |
rs369729657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947588 | GCACTTTTGGAGGCC[A/G]AGGTGGGCAGATCAC | 55833 |
rs369736836 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992585 | AAAATAAAAAAAAGA[C/T]ACCCTCCCCATCCTA | 55833 |
rs369737555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020092 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55833 |
rs369741952 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003816 | CCTCCACTTCCCAGG[C/T]TGAAGCAATTCTAGT | 55833 |
rs369742646 | snp | C/T | 0.000169762 | 0.00921152 | missense | UBAP2 | GRCh38.p7 | 9:33927815 | AGGTCACCAAGGGCG[C/T]GGCCCTGCTACTGCT | 55833 |
rs369749073 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983560 | TAATCACACACATAA[C/T]GTTGGTCTTATACTG | 55833 |
rs369749966 | snp | A/G | 3.29538e-05 | 0.00405904 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33956118 | TCTGCTGGAGCAGAT[A/G]AGGCAGTGAAGACCT | 55833 |
rs369753212 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951300 | GGGATTTACAGGGAT[A/G]AGCCACCATGCCATG | 55833 |
rs369758822 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969827 | GCCAAGATCGTGCCA[C/T]TGCACTCCAGCCTGG | 55833 |
rs369777922 | in-del | -/GTGCAGTGCCGTGATCTTGACTGT | 0.021333 | 0.101051 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999763 | GTTACCCTAGCTGGA[-/GTGCAGTGCCGTGATCTTGACTGT]GCAACCTCCGCCTCC | 55833 |
rs369778745 | in-del | -/GAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940069 | GAGGGGAAAGAAGAA[-/GAA]AAGAAAAAGAAGAAA | 55833 |
rs369856540 | snp | A/G | 4.94173e-05 | 0.00497053 | missense | UBAP2 | GRCh38.p7 | 9:33923227 | TTGTTTGGTGCCTGC[A/G]ATGATCCAGCATAGC | 55833 |
rs369862047 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008793 | AACATGGTGAAACCC[C/T]GTCTCTACTGAAAAA | 55833 |
rs369869302 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049310 | ACGAGGGGACCACGA[C/G/T]TCCCAACATGCTGCA | 55833 |
rs369878533 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956492 | CGCCACCACACCGAG[C/T]TAATTTTTGTATTTT | 55833 |
rs369902884 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934547 | TCCATATATAAACCT[C/T]GTTCATAGATAAACT | 55833 |
rs369920209 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002920 | ATTGAACCCCCCGAG[C/T]TTAAGCAATTCCTCT | 55833 |
rs369932465 | snp | C/T | 1.65353e-05 | 0.00287531 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971615 | TTAATAGCTCAAACA[C/T]TTAAAACTCATCTCT | 55833 |
rs369975942 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946747 | AGAGCTGGTTTAGGC[A/G]CATTCATTTTTGAAC | 55833 |
rs369976592 | snp | A/C | 0.00023475 | 0.0108314 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943399 | CTATTTTGCTTCATA[A/C]CAAAGGACTAAATTC | 55833 |
rs370068863 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041949 | AGAATCGCTTGAACC[C/T]GGGAGGTGAATGTTG | 55833 |
rs370105435 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042772 | GGTTGTTCATTTTAC[-/T]TTTTTTTTTTAATTT | 55833 |
rs370126193 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048541 | AACCCGAAAGGGGGG[A/T]GGGGAGGCACCCCTG | 55833 |
rs370135924 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948765 | GCAATGAAAACTGAC[A/T]AAATAAATGCAGCTA | 55833 |
rs370156752 | in-del | -/CAGCATTTTATTAAATGCTAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978167 | AACTGATTTGAGAAT[-/CAGCATTTTATTAAATGCTAT]GTGGAACAAGGACTC | 55833 |
rs370159448 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995380 | ATAAATATATAAATA[C/T]ATATATTAAATATAA | 55833 |
rs370167661 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012582 | TATAAGTATGGTCTG[C/T]AGATGTTCTGATTTT | 55833 |
rs370169081 | in-del | -/GT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959491 | CTGCTCAAACTCTGT[-/GT]CAGACAGATACCAAA | 55833 |
rs370190537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958499 | CACTGCAAGTGCCTC[C/T]CGGGTTCAAGTGATT | 55833 |
rs370222447 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927256 | GGGAGACAGAAAGCC[C/T]GGCCACCACACTGAG | 55833 |
rs370228452 | snp | C/G | 3.55461e-05 | 0.00421566 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953265 | TCTTAAAATCCCACA[C/G]TGAAATAAAAGTGAG | 55833 |
rs370230611 | snp | A/G | 7.12695e-05 | 0.00596906 | missense | UBAP2 | GRCh38.p7 | 9:33922847 | CTGAAAGGTGGAGGC[A/G]TCCCTGCATGAAATC | 55833 |
rs370270799 | snp | G/T | | | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33988998 | ACGATTGCCGCCTCT[G/T]CCTTTCCGGTTGTTG | 55833 |
rs370275867 | snp | C/T | 1.65195e-05 | 0.00287393 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973287 | TACTTATGTCCTACA[C/T]AATTACACTTCCTTC | 55833 |
rs370299605 | snp | C/T | 0.000148555 | 0.00861717 | missense | UBAP2 | GRCh38.p7 | 9:33926652 | GCATCTGGAGCTCGT[C/T]ATAGCCATAGATCTG | 55833 |
rs370304516 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000717 | CTCATTTCAAATAAT[A/C]TTGACTGAAGTGGGA | 55833 |
rs370305926 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003719 | GCCAAAGAAAGATTT[A/C]TTTCTTTTGTTTTTT | 55833 |
rs370328976 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963601 | TGATTACCAAATAAA[C/T]AGGTATAGTTTACAA | 55833 |
rs370335086 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968286 | TATACTGTCCATTTA[C/T]TCTGTACACCAAGAA | 55833 |
rs370431467 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021892 | AACCGCCTCAACCTC[C/T]CAAAGTGCTGCAATT | 55833 |
rs370437095 | snp | C/T | 3.30055e-05 | 0.00406222 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924313 | GGGAGGCTTGATCAG[C/T]GACTGGCCCTGCTTG | 55833 |
rs370475435 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038761 | CGTCTGGGATGTGAG[A/G]AGCCCCTCTGCCCTG | 55833 |
rs370501134 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950803 | TGAATCAATGACTAC[A/T]GCCATGTCCTAGGTA | 55833 |
rs370510663 | snp | C/T | 6.60251e-05 | 0.00574528 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973140 | CTGCAGAATAAAAAC[C/T]AGGGAAGTAAATAAT | 55833 |
rs370520473 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029539 | CTCAAAAAAAAAAAA[A/G]AAAATGTATACATAG | 55833 |
rs370526219 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984600 | GAAGTATCACTTGAG[C/T]CCAGGATTTCAAGGT | 55833 |
rs370535058 | in-del | -/CT | 0.000422386 | 0.0145263 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938883 | CTGTCAGGATATAGA[-/CT]CTAACTTATTTCTGT | 55833 |
rs370552063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027374 | TAATCCCAGCAAATC[A/G]GGAGGCTGAGGCAGG | 55833 |
rs370600030 | snp | A/G | 0.000647394 | 0.0179799 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932532 | CTCCCCAAGCATGGC[A/G]GAGGAAGAGGAAGCC | 55833 |
rs370649358 | snp | C/T | 1.64977e-05 | 0.00287203 | missense | UBAP2 | GRCh38.p7 | 9:33943550 | CATTTAATCCTGTGA[C/T]ATCTGCTGAACCAGG | 55833 |
rs370658862 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038684 | AAAGTGCCGAGATTG[C/T]AGCCTCTGCCCGGCC | 55833 |
rs370663663 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989798 | TACTTATTAATTCAA[A/G]GACCACAAAATTACT | 55833 |
rs370673547 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031211 | GAACCCAGGAAGCGG[A/C]GGTTGCAGTGAGTTG | 55833 |
rs370690451 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971544 | ACAGTAGCCTGTTTT[C/T]CATTCTTTTCCATCA | 55833 |
rs370725250 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | UBAP2 | GRCh38.p7 | 9:33923911 | GCTGGGCTGTGTGGT[A/G]GGTCTGTGATTGGCT | 55833 |
rs370730940 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | UBAP2 | GRCh38.p7 | 9:33948463 | GTACTATTCTGCTGT[A/G]TACTTGGGGTGGTGG | 55833 |
rs370740927 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046536 | GTAGTGCCAGCTACT[C/G]GGGAGGCTGAGCCAG | 55833 |
rs370743675 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923784 | ACAGTCACACCCTCT[A/G]AAATACTCACAAACA | 55833 |
rs370755129 | in-del | -/ACAC/ACACACACAC/ACACACACACAC/ACACACACACACACAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954269 | TAAGTGTGTGTATAT[lengthTooLong]ACACACACACACACA | 55833 |
rs370763390 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989919 | AAAATTTTAGCTTGG[C/T]TTTGGTGGGTTTTTA | 55833 |
rs370796178 | snp | C/T | 0.000116045 | 0.00761636 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998769 | TAAAAATGATGATAT[C/T]CTTTGCCAGAAACAT | 55833 |
rs370804398 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981800 | AGGAAGGAAGGAAGG[A/G]AGGAAGGGTGGAAGG | 55833 |
rs370836091 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035584 | ACTACTCAGAGGAGG[A/C]TGAGGCACAAGAATC | 55833 |
rs370853470 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977932 | AGGCAGGAGAATCCC[C/T]TGAACCCGGGAGGCA | 55833 |
rs370877086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966924 | TCAGTGGGGAAAATT[G/T]ACATGAGACGGACCA | 55833 |
rs370887310 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028887 | AGACTGGGGTAATTA[A/G]GAACTGGGCCGCACA | 55833 |
rs370931490 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994184 | CAGGCATGAGCCGCA[C/G]TGCCCAGTCAGTCTT | 55833 |
rs370951060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027810 | GAGCTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 55833 |
rs370955722 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982669 | AAAACACCATACCCC[C/G]TGCAGAATTTATCTA | 55833 |
rs370973276 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934394 | AGGAAAGAGGAGCAA[A/C]CTTGACCCTTCTAAA | 55833 |
rs370986971 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006318 | AGAAATGTCAAGAGA[C/G]ACAGAAGAGAATGAA | 55833 |
rs371013475 | snp | A/C/G | 1.64738e-05 | 0.00286995 | missense | UBAP2 | GRCh38.p7 | 9:33923845 | TGCCTGTGTAGTAGG[A/C/G]AAGACCAGTGTAGCT | 55833 |
rs371055265 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930623 | CAGATGATGGCCGGG[C/T]GCGGTGGTTCACGCC | 55833 |
rs371060169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993552 | TGGCATGCGCCTGTG[A/G]TCCCGGCTACTCGGC | 55833 |
rs371107908 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937302 | ATCTAGCATGTAGTT[A/G]AGAATACATAGTATC | 55833 |
rs371108054 | snp | A/T | 0.000198403 | 0.00995801 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924326 | AGCGACTGGCCCTGC[A/T]TGACTCCCAGGAGAG | 55833 |
rs371122770 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977719 | CCAGGCTGGAGTGCA[A/G]TGGCGTAATCTTGGC | 55833 |
rs371142324 | snp | A/G | 1.65209e-05 | 0.00287405 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927927 | TGCGGAACTTGAGAC[A/G]GAGGTCGCTGCCGTG | 55833 |
rs371191006 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044076 | GGCCTGGGTGACAGA[A/G]TGAAACTCCACCTCA | 55833 |
rs371201933 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014432 | TCAGGTGTTGGAGAC[C/T]AGGCTGGGCAACATG | 55833 |
rs371246921 | snp | A/G | 0.000121734 | 0.00780078 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944659 | AAAAAGTAAGCAGCA[A/G]TTAATGAGGCATAAT | 55833 |
rs371266837 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010427 | AGAAACTCTGCCTCA[A/T]AAAAAAAAAAAAAAA | 55833 |
rs371285510 | snp | A/G | 0.000875616 | 0.0209055 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986326 | GTAAGATGACTACTT[A/G]ACAATTACGTATTAT | 55833 |
rs371321080 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951134 | ATGCCAGCCTCTCAA[A/G]TAGCTGGGATTACAG | 55833 |
rs371331701 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030428 | CACTCCAGCCTGGGC[A/G]ACAGAGCCAGATTCC | 55833 |
rs371335700 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976139 | TTACAAGAATGTTAA[G/T]AAATTCAGCTAATTA | 55833 |
rs371351152 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939562 | AGATTCCTTGAGACT[A/G]GCCTGGGTAACATGA | 55833 |
rs371395227 | snp | C/T | 0.000185998 | 0.0096418 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953502 | AAAGCAATGAGGAAC[C/T]AGTCATAAGCAAATC | 55833 |
rs371406239 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942742 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAC | 55833 |
rs371486819 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923040 | CTGATACTCCTAGGA[A/G]GAAAAGCAGTTGTTC | 55833 |
rs371497703 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002740 | TGCAATGGCACAATC[A/T]GTGCTCACTACAGCT | 55833 |
rs371562287 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036806 | ACCTTAAGTTTTTCT[-/C]TTTTTTTTTTTTTTT | 55833 |
rs371590234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018680 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 55833 |
rs371605403 | snp | A/G | 1.65688e-05 | 0.00287821 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33988980 | GTACTTACATTCTCT[A/G]CCACGATTGCCGCCT | 55833 |
rs371610033 | in-del | -/ACTC | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988285 | CACTACATAGTAGAT[-/ACTC]AATAAATATCAGTGG | 55833 |
rs371610450 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965451 | TACAATTTTTGATAA[A/G]ATGTACTTTGTCAAT | 55833 |
rs371616706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980823 | ATAGTAGCGTGCACC[C/T]GTAGTCCCAGCTACT | 55833 |
rs371616879 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032649 | GTTTCTTAGGCTGGG[A/T]GTGGTGGCTCATGCC | 55833 |
rs371620353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002567 | ATTTTTAGTAGAGAA[C/T]GGGTTTCACAATGTT | 55833 |
rs371660381 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012840 | TAAATCTCACAATGT[A/T]TTTTTTTTTTTTTTA | 55833 |
rs371671353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005106 | CGTCTACACTAAAAA[C/T]ACAAAAATTAGCAGT | 55833 |
rs371674945 | snp | A/G | 1.73769e-05 | 0.00294757 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922543 | GCCGTAGGCAGGTTT[A/G]GAGGCTTGAGACTTG | 55833 |
rs371741175 | snp | A/C | 1.64863e-05 | 0.00287104 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924038 | GCCACTGCCCTTCCT[A/C]CAACCAGAGAAAGGC | 55833 |
rs371757895 | snp | G/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935840 | GCTGCTATACTTACT[G/T]TCTAGTGTCTGCTGA | 55833 |
rs371760116 | in-del | -/GAGGAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016246 | GAGGAAGGGGAGGAA[-/GAGGAG]GAGGAGGAAGAGGAG | 55833 |
rs371780113 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026326 | GTGCAAAGTATCTCA[A/G]CTACTACATCAAATA | 55833 |
rs371794451 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991162 | GTGGTGGCAGGCACC[C/T]GTAATCCCAGCTACT | 55833 |
rs371816209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935333 | TTTTTCTTTTCAGAC[A/G]GAGTCTCACTTTGTA | 55833 |
rs371851905 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956017 | ATGAAAATACTTTTC[C/G]TGAGGCAAAAGATTT | 55833 |
rs371858887 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019565 | GAGTTTCTGTAGGGG[A/T]GGATACAAAGGTTCG | 55833 |
rs371914504 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022434 | CACAGCAAGACCCCT[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs372020226 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969042 | TTATTCCATTCTATG[C/T]ATATTCTATATTTTG | 55833 |
rs372024465 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924897 | AAACATGAAATTTGT[G/T]TGCAATTTTTTTAAG | 55833 |
rs372025774 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006204 | GCACCATTGCACTCC[A/T]GCCTGGGAGACAGGG | 55833 |
rs372025919 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940263 | TTCTCAGCTGCCTAC[A/G]CCAAGTAAGATGCTG | 55833 |
rs372037270 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027434 | ATAAACAAAAGAATC[G/T]GGCCTGGCATAGTGG | 55833 |
rs372077505 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996926 | TTACAAAAAATTAAC[C/T]GAGCGTAGTGGTAGG | 55833 |
rs372164227 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993111 | CAGTACTTATGTTCA[A/G]TATCTTCCTTTGTGA | 55833 |
rs372170470 | snp | A/G/T | 0.00019779 | 0.00994273 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924169 | AGTTCGCGCTAGGCC[A/G/T]GCCCCGGGCTACTCC | 55833 |
rs372173073 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33960864 | TCCACTCTTCCACAG[A/G]ATTCTTCCAAGCCCC | 55833 |
rs372220465 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989135 | ATGAAGTCTATCAGA[A/G]AGAACGGCTGTTAAT | 55833 |
rs372292380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031984 | ATCTCTACTAAAAAA[C/T]ACATTTAAAAATTAG | 55833 |
rs372300223 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939582 | GGGTAACATGATGAA[A/C]CCCCATCTCTACAAA | 55833 |
rs372325804 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935716 | AAAAACAAAAAAGCA[A/T]AAGGGCTGCTTTTTA | 55833 |
rs372337371 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974185 | ACATAGCAAGACTCT[C/G]TCTCAACAACAACAA | 55833 |
rs372365876 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981184 | ATATATATATTCTGG[-/AT]ATATATATATATATA | 55833 |
rs372372957 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008637 | AAAGCGTAAGATATA[A/T]ACTAACACTTTACAG | 55833 |
rs372408518 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933280 | CCCAGTGCTCTGTGC[C/T]AGCAGAGGCGGTACA | 55833 |
rs372412105 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33944472 | TGGGAAGCTGCAAAA[A/G]CTTGTTCACAGTGGA | 55833 |
rs372451986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037846 | AAATACAGAAACCCC[A/G]ACTGGATGGGAAAGA | 55833 |
rs372479747 | snp | A/C/G | 4.99388e-05 | 0.00499669 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998908 | TTGAACACCAAAAGC[A/C/G]TAAGTTAGATTCCAA | 55833 |
rs372495953 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982424 | GAACAAAAACCAAAA[A/C]AAATAAAAAATAGGT | 55833 |
rs372502910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925310 | ACACACAGAGCTGCA[C/T]AACTGAGGACGGGAG | 55833 |
rs372529460 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977151 | TCAGGCAATTCTCCC[A/G]CCTCAGCCTCCTGAG | 55833 |
rs372562789 | snp | A/C/G | 3.2948e-05 | 0.00405871 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923819 | GGGGCCATACTGGAA[A/C/G]GCACTGGGCATGCCT | 55833 |
rs372576308 | snp | A/G | 0.000725343 | 0.0190301 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932651 | ACAAAACAGAGCGCC[A/G]TATGTCCACCTGAAC | 55833 |
rs372577001 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974991 | ATGGATTTCTCCAAA[A/G]AAGATATACAAATGA | 55833 |
rs372584286 | in-del | -/A/AA | 0.499732 | 0.0115784 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014773 | GACAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 55833 |
rs372584690 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992906 | AGGTCCTCCCAGCCA[A/C]CACATAATAATCAGA | 55833 |
rs372609383 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936631 | CATGGGCAACAGAGC[A/G]ACACTCCATCTCAAA | 55833 |
rs372611687 | snp | A/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957005 | TGAGGCAGGAGAATC[A/G/T]CTTCAGTCCAGAGGT | 55833 |
rs372618667 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012869 | TAAATTGAGGTTCAC[A/G]GTCAGGCCCAGGGGC | 55833 |
rs372621970 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034805 | TTCAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGT | 55833 |
rs372623708 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985698 | GGGAATAAAGAGAGA[C/G/T]TGGTGGATAGGTTAA | 55833 |
rs372636472 | snp | A/G | 1.65031e-05 | 0.00287251 | missense | UBAP2 | GRCh38.p7 | 9:33941653 | ATACCACTTACCATG[A/G]TGGTTCCTGGAGCTG | 55833 |
rs372644288 | snp | A/G | 4.96537e-05 | 0.00498241 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948598 | GATGACTTTAAAAGG[A/G]GGATAAAAGAACAAA | 55833 |
rs372644697 | snp | G/T | 0.00179452 | 0.0299005 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960886 | CCAAGCCCCTGTTGG[G/T]AAACAACAGCAATCA | 55833 |
rs372684166 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930091 | AATATATAAAAAAAA[-/A]GGATGTACAACCTCA | 55833 |
rs372705013 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029653 | CCAGCCTGGGCAGCA[C/T]AGCAAGACCTTGTCT | 55833 |
rs372740309 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042427 | AGGTTGCAGTGAGCT[C/G]AGATCGGGCCACTAC | 55833 |
rs372740433 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969896 | AAAAAAACCAGTTAA[G/T]CAAACTTAAATACCG | 55833 |
rs372743079 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009680 | ACTCAGGCTGGTCTC[A/G]AACTCCTGGACTCAA | 55833 |
rs372747067 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986680 | GAACACACTGCCATC[C/T]CTAGTCACAGTCCAG | 55833 |
rs372761897 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931937 | TCCAGCCTCTCTTAA[C/G]TTTTCATTGCATGCC | 55833 |
rs372764996 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992337 | GAGGTTGTGGTGAGC[C/G]GAGATCACGCCATTA | 55833 |
rs372777943 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996036 | GTCATCAGATTCTAC[A/G]ACTTCATGAAGAAAC | 55833 |
rs372800640 | snp | C/T | 0.00021507 | 0.0103677 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926711 | ACCACATACCACACC[C/T]TGGGAAGCCCAGGTC | 55833 |
rs372807616 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959561 | GGTATAAAATTTTAT[C/G]GTATTGGGTTATTTA | 55833 |
rs372824154 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936347 | TCACCCAGGCTGGAG[C/T]GCAATGGCGCATCTT | 55833 |
rs372836688 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986725 | GCTTCTTCCCCCTAA[C/T]TGAAAGCATTTTCTT | 55833 |
rs372841598 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947938 | AGACTGCTTGAGGCC[A/C]GGAGGTGGAGATCAG | 55833 |
rs372845646 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010321 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGGGAAAA | 55833 |
rs372871419 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937927 | CCTCTCAAAAAATAG[A/G]TACATATATTTACAC | 55833 |
rs372893129 | snp | A/C | 6.65447e-05 | 0.00576783 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922918 | GAAGGTCAGGTTGGG[A/C]TGTAACCTCTCAAAA | 55833 |
rs372925857 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035514 | CTAAAAAAAAAAAAA[A/T]ATATATATATATAAA | 55833 |
rs372958217 | in-del | -/GGAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981855 | GGGAAAGGGAGGGAG[-/GGAA]GGAAGGAAGGAAGGA | 55833 |
rs372994782 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992659 | AACTTATCGGGCGGA[-/G]GGGGGGGGGCACAAA | 55833 |
rs373015894 | snp | C/T | 5.01349e-05 | 0.00500649 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33926989 | CCGCCATACACTCAC[C/T]GGGTAGGCAGGAAGC | 55833 |
rs373016429 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993864 | AGAGGTAACCAAAGA[A/G]GTGTTCTTCATGAAA | 55833 |
rs373021130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045594 | GGTTAGGTTAGTCTC[A/G]AACTCCCGACCTCGT | 55833 |
rs373028963 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003389 | GCTTTTTTTTTTTTT[G/T]TTGAGACAGTCATGC | 55833 |
rs373052545 | snp | A/G | 3.31356e-05 | 0.00407022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998876 | TTGCCTGGAAAGTAC[A/G]TACAATTGTTAAGGA | 55833 |
rs373080142 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049349 | GCGACCCCTACCGCA[C/G]CCTTTCTCCAGCGGG | 55833 |
rs373102202 | snp | A/G | 3.30781e-05 | 0.00406669 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971759 | GATTAAATGTCCTGG[A/G]GTTTGAAATAAAGAA | 55833 |
rs373130260 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971794 | TAAAGGCAAAAGAAG[C/G]AAACACCTAAGCCAA | 55833 |
rs373200909 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944687 | AATGGCTTCACAATG[C/T]TCTTCAATAGAACAT | 55833 |
rs373269799 | in-del | -/AAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962646 | AAGACTCTATCTCAA[-/AAAT]AAATAAATAAATAAA | 55833 |
rs373329326 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967306 | CCTTTCCAATCCTTA[G/T]GACTTACTTATTTTT | 55833 |
rs373366366 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030595 | GCCAGTGCACTCCTA[C/G]TACAGTGCCCAAGAG | 55833 |
rs373377336 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014876 | AAATTTTTCCATCAC[C/T]GGACTAGATCAGTTT | 55833 |
rs373392660 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007389 | TAGTCCCAGCTACCC[A/G]AGAGGCTGAGGCAGA | 55833 |
rs373418057 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954032 | GTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55833 |
rs373424087 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029380 | TAAAAATATAAAAAA[A/T]TAGCTGGATGTGGTG | 55833 |
rs373426087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941485 | TCAAGAGCATGGGTG[C/T]TAGAGATGCCCACTA | 55833 |
rs373439521 | snp | A/C/T | 6.61436e-05 | 0.0057505 | missense | UBAP2 | GRCh38.p7 | 9:33927845 | TGCTGGATGCACTCG[A/C/T]GGGGGTCCCACCCAG | 55833 |
rs373444652 | snp | A/G | 4.95029e-05 | 0.00497484 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956156 | AGAAAGCTGTATGGA[A/G]AGTTGAAAAATTTAA | 55833 |
rs373507878 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935773 | TTTTCCACATCACGT[A/G]AGCTATCCTCTTCCT | 55833 |
rs373522628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936901 | AGTTCATGACCACCC[C/T]GGGCACTGTAGCAAA | 55833 |
rs373554928 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040885 | TGTTCTGTGGTTCAG[C/T]TGACAAGCCTGAGAA | 55833 |
rs373590717 | snp | C/T | 0.00019771 | 0.00994062 | missense | UBAP2 | GRCh38.p7 | 9:33943472 | TACTATTTTCACTGC[C/T]TGGAGCTGATCCAAA | 55833 |
rs373613413 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020378 | CAGGCTGGAGTGCAA[C/T]GAATAGTGCGATCTC | 55833 |
rs373616628 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986631 | GGCATCAGTAAACAA[-/A]TGATCAGATTTTAGA | 55833 |
rs373651964 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045099 | ACCCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 55833 |
rs373679193 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049109 | AGGGAGACTTGATAA[C/T]ATGTATTGTACTCGG | 55833 |
rs373685027 | in-del | -/CAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942440 | AAACTAAAACAACAA[-/CAA]CAACAAAGTCAGCCA | 55833 |
rs373694617 | in-del | -/CATTTACTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046073 | GAGCTCCATTTACTC[-/CATTTACTC]AAAATAACAACTAAG | 55833 |
rs373703211 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBAP2 | GRCh38.p7 | 9:33941791 | GTCAGACTGCAGGAG[A/G]TAATGACGGAAGTTG | 55833 |
rs373709151 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951663 | CCAGTGATTTTTAAA[C/G]ATTAGAGTAGGGTCG | 55833 |
rs373744232 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952502 | TTAAGAAAATGTAGC[-/T]TATTTTACGGTCTTA | 55833 |
rs373757819 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968434 | ATACATAGTCATGGC[C/T]GAGGGCATGTGCAGC | 55833 |
rs373837334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959663 | CTGACAGTACCCAGA[A/C]GCTAGTGTAACATGC | 55833 |
rs373888009 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998662 | CCAAAATCCAATATA[C/T]AGATTTCAGGTGAGA | 55833 |
rs373918621 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035698 | TCAAAAATAAAGAAA[C/G]AAACAAACAAACACT | 55833 |
rs373922170 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988794 | ATTGAGGAAACGAAT[C/T]TATGAGCATACTATG | 55833 |
rs373957432 | in-del | -/AGG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955282 | TCCCAGCACTTTAGG[-/AGG]CCGAGGCTGGCGGAT | 55833 |
rs373973111 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938525 | TCATTGGCCGGGCGT[A/G]GTGGCTCACGCCTGT | 55833 |
rs373977383 | in-del | -/AATAGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016190 | AGGAGGAAGAGGAGG[-/AATAGA]AGGAAGAGGAGGAAT | 55833 |
rs374002146 | in-del | -/TT/TTTTTT | 0.453575 | 0.145111 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990637 | AATAGTACCCCCCAA[-/TT/TTTTTT]TTTTTTTTTTTTTTT | 55833 |
rs374020251 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982649 | ATAGGAAGAACAGGT[C/G]AAATAAAACACCATA | 55833 |
rs374091265 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941915 | CTTTAAATAGCTTCA[A/T]AAAAAAAAAAAAACA | 55833 |
rs374134621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951535 | TATTTTTAGTAGAGA[C/T]GGGGTTTTACCACAT | 55833 |
rs374138410 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930664 | CCACTTTGGGAGGCC[A/G]AGGCGGGTGGATTAC | 55833 |
rs374181118 | snp | A/G | 0.000741174 | 0.0192364 | missense | UBAP2 | GRCh38.p7 | 9:33922970 | TTGTCCCTCACCTGT[A/G]TCTTATTGTAGACAG | 55833 |
rs374183605 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023690 | GTTTTTCTCTTAATT[A/T]AGGTTTACTGCTCTG | 55833 |
rs374194311 | snp | C/T | 0.000908918 | 0.0212987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986749 | TTTTCTTCCCTCTTA[C/T]TCTAGCTTACCTCTA | 55833 |
rs374205238 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006086 | AAATACAAAAAAATT[A/C]GCCGGGCATGGTGGC | 55833 |
rs374207712 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994466 | TCCCAAAGATTTTTT[C/T]TTTTTTTTTTTTTTC | 55833 |
rs374214011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044853 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTGTAA | 55833 |
rs374220194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041893 | AGCCAGGCATGGTGG[C/T]GGGCACCTGTAGTCC | 55833 |
rs374228475 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007730 | TGCAAGCTCTGCCTC[C/G/T]CCGATTCACGCCATT | 55833 |
rs374233416 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926238 | CTCTGAGGAAGAGGA[A/T]GACAGTATAAAACTC | 55833 |
rs374235115 | snp | A/G/T | 6.60048e-05 | 0.00574445 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996343 | CATAAGCTAGTGAAC[A/G/T]TATCAGAAAATGGTT | 55833 |
rs374241551 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992058 | GGAGTTCCAGACCAC[C/G]CTGGCCAACATGGTG | 55833 |
rs374250092 | snp | A/C | 3.31225e-05 | 0.00406941 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924333 | GGCCCTGCTTGACTC[A/C]CAGGAGAGCAGAACC | 55833 |
rs374294705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038719 | CCCCGTCTGGGAAGT[A/G]AGGAGCATCTCTGCC | 55833 |
rs374310061 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022410 | CACAGTTCAAATCCA[A/G]GCTAGGCAACACAGC | 55833 |
rs374324412 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027811 | AGCTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 55833 |
rs374333557 | snp | C/G | 1.98096e-05 | 0.00314713 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928028 | ACACATGGATCTGGA[C/G]GCAGAGGAGGAGGGT | 55833 |
rs374334187 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948761 | CTATGCAATGAAAAC[G/T]GACTAAATAAATGCA | 55833 |
rs374340861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928232 | CAAAACTATTAACAT[G/T]AAGCTTTAATGACCA | 55833 |
rs374350605 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978656 | GTGCTGGCGGGTGCC[-/T]ATAGTCCCAACTATT | 55833 |
rs374357738 | snp | C/G/T | 6.58907e-05 | 0.00573948 | missense | UBAP2 | GRCh38.p7 | 9:33948476 | GTGTACTTGGGGTGG[C/G/T]GGTAAACTGGCCCAA | 55833 |
rs374375189 | snp | A/C/G | 8.21569e-05 | 0.00640872 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017007 | AGTATAATAATAAAA[A/C/G]AAAAAAAAGGAAAAA | 55833 |
rs374425169 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923088 | CAGCTCCAGGCTCCC[C/T]ACCTCCAGGATCACT | 55833 |
rs374612343 | snp | C/T | 8.26685e-05 | 0.00642864 | missense | UBAP2 | GRCh38.p7 | 9:33948404 | CTGAGGACTGGGATG[C/T]TGGGGGCTTGAGGTC | 55833 |
rs374635116 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969074 | TTATACATTCATCCA[C/T]TGATAAACATTTGAG | 55833 |
rs374637959 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003995 | AAAGTGCTGGGATTA[C/T]AGGTATGAGCCACCA | 55833 |
rs374645219 | snp | C/T | 4.94328e-05 | 0.00497131 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960882 | TCTTCCAAGCCCCTG[C/T]TGGGAAACAACAGCA | 55833 |
rs374661162 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995067 | TCAATTTAAGAAACA[A/T]AAACACAGGTCAGGT | 55833 |
rs374665688 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028929 | GCAAACCTGGGCGGC[A/G]TGGCAAGTCCTCGTC | 55833 |
rs374690576 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935878 | CACCACCATGTCCAT[C/T]CTATAAGGAAAAGAA | 55833 |
rs374697433 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029665 | GCATAGCAAGACCTT[C/G]TCTCTATTTAAAAAA | 55833 |
rs374710350 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008638 | AAGCGTAAGATATAT[A/T]CTAACACTTTACAGA | 55833 |
rs374717091 | snp | A/G/T | 0.000381581 | 0.0138074 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932548 | GAGGAAGAGGAAGCC[A/G/T]CGCAGACACTTACTG | 55833 |
rs374730198 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014560 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCTGTGAA | 55833 |
rs374744417 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033256 | AAAACATGGTACTTA[C/T]ACACAACAGAGTACT | 55833 |
rs374776694 | snp | A/G | 6.59141e-05 | 0.00574045 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33973229 | CTCTCCCTCTGCCAC[A/G]TCCAAATCCTTTAAA | 55833 |
rs374807402 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944666 | AAGCAGCAATTAATG[A/T]GGCATAATGGCTTCA | 55833 |
rs374821095 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989000 | GATTGCCGCCTCTTC[C/G]TTTCCGGTTGTTGTT | 55833 |
rs374836360 | snp | A/C | 1.64906e-05 | 0.00287142 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924050 | CCTCCAACCAGAGAA[A/C]GGCCACACTGGCTTC | 55833 |
rs374839915 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010455 | AAAAAAAAAAGACAA[A/T]AAACAAATAATACAC | 55833 |
rs374842162 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037280 | GGCGTGAGCCACCGC[A/G]CCCAGCCCACACACA | 55833 |
rs374851332 | in-del | -/AACAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942426 | ATGTGAAAAAACTAA[-/AACAA]CAACAACAACAAAGT | 55833 |
rs374889208 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012601 | TGTTCTGATTTTTTA[A/T]AATTGTACTGTAATT | 55833 |
rs374895421 | snp | A/C | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050722 | AAAAAAATGTCCGGG[A/C]GCGGTGGCTCACGCC | 55833 |
rs374901784 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925188 | CCCTTGGGCTGTGCC[C/T]GATCCCAGAAAGGAG | 55833 |
rs374907914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959018 | GCCAGGCATGGTGGC[A/G]TGCATCTATAATTCC | 55833 |
rs374912419 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042782 | TTACTTTTTTTTTTT[-/T]AATTTTACATATGGG | 55833 |
rs374940505 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005490 | CATATCTCTAAGTTT[C/T]TCTATTTCTTCTTTA | 55833 |
rs374943802 | snp | C/T | 0.00018125 | 0.009518 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986712 | AACGCAACTGCCTGC[C/T]TCTTCCCCCTAATTG | 55833 |
rs374963278 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038920 | GGATGTGGGGAGCGC[C/T]TCTGCCCCGCCACCC | 55833 |
rs374964565 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991309 | CTGTATCAAAAATAA[A/T]AATAATAATAACGTA | 55833 |
rs374964870 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969776 | GACACTGAAGCAAGA[C/G]AATCGCTTGAACCTG | 55833 |
rs374970219 | snp | G/T | 0.000115499 | 0.00759844 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923066 | TGTTCCCCACAGCAG[G/T]TGTTCCCAGCTCCAG | 55833 |
rs374979517 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934799 | GCCTAGACAAAAGAA[A/C]CCTGCCACTACCACT | 55833 |
rs374992595 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983366 | TCATGAAGATTTGAC[A/G]ATTTCTCTAAGACGC | 55833 |
rs375001232 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981801 | GGAAGGAAGGAAGGA[A/T]GGAAGGGTGGAAGGG | 55833 |
rs375010413 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988519 | TCTAACCCTTGTCTA[C/T]ACCATGAGTGTCTAT | 55833 |
rs375015213 | snp | A/G | 8.43875e-05 | 0.00649512 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922903 | AAAGAAGACAATGGT[A/G]AAGGTCAGGTTGGGC | 55833 |
rs375028197 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036602 | ACATGTAAGCAACTG[A/C]AGATCAGGAACCTAC | 55833 |
rs375029038 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936441 | TGGGATTACAGGCGC[A/G]CACCACTACACCAGG | 55833 |
rs375029814 | snp | A/G | 1.65263e-05 | 0.00287452 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926681 | TGTGTGAGAACCAGA[A/G]AGTGTATTTTAGGAA | 55833 |
rs375034750 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956847 | AGGTGGCCAGGAATG[A/G]TGGCTCACACCTGAA | 55833 |
rs375060716 | snp | C/G | 1.64849e-05 | 0.00287092 | missense | UBAP2 | GRCh38.p7 | 9:33944537 | GCCTGGGAAGGAAAG[C/G]ACTCCAAACCAGGAG | 55833 |
rs375156584 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987513 | CTCAGGAGGCTGAGG[C/T]GGGAGGATCACCTGA | 55833 |
rs375179045 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958116 | ACAGGCACCTGCCAT[C/T]ACACACAGCTATTTT | 55833 |
rs375195308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036239 | CCTCCTCCTCAGCCT[C/T]CCAAGTAGCTGGGGT | 55833 |
rs375204808 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976229 | CAAGCTACAAAACAA[A/G]GAAACTATTCTCAGG | 55833 |
rs375227543 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935173 | AGTGGCGGGGGGGGG[-/GGG]TCTCATTTTCTCCCA | 55833 |
rs375243242 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989819 | CAAAATTACTTAGAA[A/T]GATGCCCCAAAAGCT | 55833 |
rs375245273 | snp | A/G | | | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922810 | GGCCAGGGGCCCAGT[A/G]GAGCCCAAGACCGAG | 55833 |
rs375258303 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958374 | ACTATAAACATTGAC[A/G]TATCTAAACATGATA | 55833 |
rs375259334 | in-del | -/CACTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015257 | TATCTCACTTCACTT[-/CACTT]AAAATAATAATATAA | 55833 |
rs375267735 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954510 | ACCGTATTACCTAAC[C/T]TTGTAATGAATGCCA | 55833 |
rs375276983 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBAP2 | GRCh38.p7 | 9:33922769 | TGTAGGAATGGTGGG[A/G]GTGCATAGCCAGGGG | 55833 |
rs375282777 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943606 | TGAAAAAGCAAAGCT[A/G]TCGTGTCAGGAACAG | 55833 |
rs375393725 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031234 | GTGAGTTGAGATCGC[A/G]CTACTGCACTCCAGC | 55833 |
rs375400971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923662 | CCTTGTCCCCAGCCT[C/G]AACAGTTTCTGAAGA | 55833 |
rs375432127 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031692 | ATGTACCACCATGCC[C/T]GGCTAATTTTTGAAT | 55833 |
rs375463502 | snp | C/T | 3.29712e-05 | 0.00406011 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989073 | ATTCTCTTTGTTTTC[C/T]GAATTTTCTTTTGCA | 55833 |
rs375469636 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926898 | GGGCAGCTCAAGGTG[C/G]GCAACCTGGGCCCAA | 55833 |
rs375474987 | snp | A/C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032956 | ATCTTTGCTTCTTGA[A/C/T]ACTCTAAGCCACAAT | 55833 |
rs375541014 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923875 | TATAGCCAGGTGGCA[A/G]TGCAGGATTCACGAA | 55833 |
rs375573509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985856 | GTAAAACCCCATGTC[C/T]AGCAAAAATACAAAA | 55833 |
rs375638224 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938907 | ATTTCTGTCAAAGCA[C/T]CTCTGAGAAGGTAAT | 55833 |
rs375638621 | snp | C/G | 1.65597e-05 | 0.00287743 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933646 | GGAACAGATGAAGTA[C/G]CTGTAAGAAGCAGAT | 55833 |
rs375705047 | snp | A/C/G | 0.000214589 | 0.0103562 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953443 | CTTGACTGTGAGGAA[A/C/G]AGGCTTCTGGAGCAA | 55833 |
rs375724382 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048168 | GAAAGAATAACATTT[C/T]GAGTATGTATTATTA | 55833 |
rs375756971 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019588 | AAGGTTCGGAAGATG[C/G]ACGGCAGTGGTGGTT | 55833 |
rs375770890 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33948526 | TCCAAAATCTGGGAG[C/G]TGGTGATGTTTGCCA | 55833 |
rs375786280 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017532 | CCAAAACAACATTGC[A/C]CCCAGCCAAGATTTT | 55833 |
rs375786634 | snp | A/G | 0.000233034 | 0.0107918 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927013 | AGGAAGCAGTCCTCC[A/G]GGACCTACGAGGTAC | 55833 |
rs375799222 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946288 | TTGAGTATTTTTTTC[A/G]TTGTTTGTCTGCCTA | 55833 |
rs375831328 | snp | C/T | 0.00152592 | 0.0275796 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953250 | GCTAATGGGTATATT[C/T]CTTAAAATCCCACAC | 55833 |
rs375855166 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961268 | ATATAGTCTTCAAAA[C/T]AACAAATTTCATTTT | 55833 |
rs375865119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042370 | ATAATCCGAGCTACT[C/T]GGGAGATGGAGGCTG | 55833 |
rs375876354 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008102 | ATCGCGCCACTGCAC[C/T]CCAGCATGGCGACAG | 55833 |
rs375878545 | in-del | -/A/AA/AAAA/AAAAA | 0.478498 | 0.1531 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960780 | GTGAAATTCCATTTC[-/A/AA/AAAA/AAAAA]AAAAAAAAAAAAAAA | 55833 |
rs375879109 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985701 | AATAAAGAGAGATTG[C/G]TGGATAGGTTAAAAC | 55833 |
rs375892407 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955603 | GGAGGCTGAGGTGGG[C/T]GGATCACCTGAGGTT | 55833 |
rs375947306 | in-del | -/ATACAA | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954726 | TTCACTGAATCATAA[-/ATACAA]TAGAGAATATGTGCA | 55833 |
rs376006591 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923083 | GTTCCCAGCTCCAGG[A/C]TCCCCACCTCCAGGA | 55833 |
rs376013810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006169 | ACCCGGGAGGCCAGA[A/G]GTTGCAGTGAGCCGA | 55833 |
rs376019970 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039010 | GTCTCTGCCCGGCCG[A/C]CCCGTCTGAGAAGTG | 55833 |
rs376026159 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | UBAP2 | GRCh38.p7 | 9:33924244 | CTCCCATCTCGGCTG[A/G]CAAGCGCTGTGGGTG | 55833 |
rs376069380 | in-del | -/TAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937753 | TCTCTATTTAAAAAA[-/TAC]AAAAAAAAAAAAAAA | 55833 |
rs376094780 | snp | A/C | 5.03419e-05 | 0.00501681 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926978 | GGCCAGGAGTTCCGC[A/C]ATACACTCACCGGGT | 55833 |
rs376121196 | snp | A/G | 0.000131965 | 0.00812203 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927915 | GGCGCCTGAGGATGC[A/G]GAACTTGAGACGGAG | 55833 |
rs376127504 | snp | A/C | 3.31598e-05 | 0.00407171 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956176 | GAAAAATTTAATCTT[A/C]TTCTACATACTACTA | 55833 |
rs376158241 | snp | A/C/T | 3.53296e-05 | 0.00420283 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932654 | AAACAGAGCGCCGTA[A/C/T]GTCCACCTGAACAAG | 55833 |
rs376166424 | snp | A/G | 1.66782e-05 | 0.0028877 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948629 | TCCTCAACAATACAG[A/G]ATTTCTGCCCAAGGC | 55833 |
rs376171279 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979230 | GTAACAGAGTGAGAC[C/T]CTGTCTCTAAAAAAA | 55833 |
rs376252701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010344 | TGGGAAAATCACTTG[A/C]ACCTGGGAGATGGAG | 55833 |
rs376253966 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043115 | CCAACCACCTTCTAC[A/G]TTATACAATGACAAC | 55833 |
rs376270359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023947 | TACCCAGGAGGCTGA[C/T]GCAGGAGAATCGCTT | 55833 |
rs376296845 | snp | C/T | 8.26959e-05 | 0.0064297 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986889 | TCCAAACCTCTTGTA[C/T]ATAACCTTATCAAGC | 55833 |
rs376308701 | snp | C/G | 4.94817e-05 | 0.00497377 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924052 | TCCAACCAGAGAAAG[C/G]CCACACTGGCTTCTG | 55833 |
rs376337472 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028132 | ACTCCCCTACACCCA[C/G]ACTTCGCTGACAGAA | 55833 |
rs376359812 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035516 | AAAAAAAAAAAAAAA[A/T]ATATATATATAAAGA | 55833 |
rs376363964 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975227 | ACGAGGTCAGGAGTT[C/G]AAGACCAGCCTGGCC | 55833 |
rs376366242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993178 | TAAAAACATCATGGA[C/T]GATTCCACTTAACAC | 55833 |
rs376406438 | in-del | -/AT | 0.449706 | 0.150391 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981303 | ATATATATATTCTGG[-/AT]ATATATATATATCTA | 55833 |
rs376423428 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009689 | GGTCTCGAACTCCTG[-/G]ACTCAAGCAATCCTC | 55833 |
rs376430921 | snp | A/C | 3.3006e-05 | 0.00406226 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963823 | AATTGAGGGTTTAAA[A/C]ATATGAAAAGAATGA | 55833 |
rs376434497 | snp | G/T | 3.30655e-05 | 0.00406591 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924324 | TCAGCGACTGGCCCT[G/T]CTTGACTCCCAGGAG | 55833 |
rs376449506 | in-del | -/GCGGCA | 0.418974 | 0.184249 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016360 | GAGGAGGCAGCAGCG[-/GCGGCA]GCGGCGGTGGTGGTG | 55833 |
rs376497666 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989496 | GTGAGCCACCGCGCC[C/T]GGCACATGCACGTAT | 55833 |
rs376521586 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962007 | CAGATGTTTCAAAAC[C/T]GAAAACATTTAATTC | 55833 |
rs376552277 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028937 | GGGCGGCGTGGCAAG[A/T]CCTCGTCTATACAAT | 55833 |
rs376571164 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971158 | CAAAGAACTCTATAT[-/A]AATAACCAATATTTA | 55833 |
rs376599549 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968248 | CATTGTAAACAGGAA[A/G]CTGGATGCAAGTCCT | 55833 |
rs376635688 | snp | C/T | 6.58913e-05 | 0.00573945 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923298 | GTCGTCATAACCTAG[C/T]GTGGCAGGGTACAAG | 55833 |
rs376640775 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002823 | TTCCCCCAATAGCTG[A/G]GAATACAGGCGCACA | 55833 |
rs376722578 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037562 | ATATTTTTAGACTTT[A/C]CAAAAGCCCCAAAAA | 55833 |
rs376732733 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041168 | TACTATAAGAAATCA[A/G]CGGGCCGGGCACGAT | 55833 |
rs376750003 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937159 | AAAGTGAAAATTATA[C/T]TGCATGGTAGCACAT | 55833 |
rs376765185 | snp | A/G | 5.04757e-05 | 0.00502348 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922461 | CGTGTGTTCTCTCCT[A/G]CCCAGGATAAGCCTT | 55833 |
rs376774621 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943520 | CTGACCCAAATTCCA[A/G]AGCCCCAAACTGCAC | 55833 |
rs376849409 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976822 | GCCAACATGGTGAAA[A/T]CCCATCTCTACTAAA | 55833 |
rs376852249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021720 | CTCACTGCAACCTCC[A/G]TCTCCCGGGTTCAGG | 55833 |
rs376865325 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984014 | CTTCCCCCAGTTCTC[A/G]TGCCTCAGCGTCCCG | 55833 |
rs376866415 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049519 | CTGGCGGGGGGTGGG[A/G]TTCCGCTCCCACGTT | 55833 |
rs376895176 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964286 | AGGCCTCTGGAAAAA[-/C]CAGCCAGCACCATCA | 55833 |
rs376947939 | in-del | -/ATAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981205 | ATATATATATTCTGG[-/ATAT]ATATATATATATATA | 55833 |
rs376968021 | snp | A/G | 7.205e-05 | 0.00600165 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922656 | AACCCCTGGCCCAGA[A/G]TAGGGTGGCTGCCTC | 55833 |
rs376978171 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963553 | ACCTTGAAAGTCAAT[C/T]AATAAAACATTTCCA | 55833 |
rs376994988 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957663 | TTATGTTTTCAATGT[G/T]GGGACTCGGCTTTGA | 55833 |
rs377017303 | snp | C/G | 8.41248e-05 | 0.00648501 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926974 | GGCAGGCCAGGAGTT[C/G]CGCCATACACTCACC | 55833 |
rs377021414 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33923820 | GGGCCATACTGGAAG[A/G]CACTGGGCATGCCTG | 55833 |
rs377047672 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999093 | CCAAACGACCTAAAG[C/T]TATTGTTCATCTTAA | 55833 |
rs377054389 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033882 | CTGGGATTACAGGCA[A/C]CCACCACCATGCCTG | 55833 |
rs377062394 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039666 | CAGTTAAGAGTCATC[A/T]CCACTCCCTAATCTC | 55833 |
rs377079397 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976080 | TAATAAATGTTTTTT[-/T]AAGAAGGCAAAAGTA | 55833 |
rs377087431 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029698 | AAAAAGAAGAAGAAG[A/G]AAGAAATGCGGCCAG | 55833 |
rs377097451 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931699 | CAGATCCAGAGGAAA[A/G]GACAGGATGTCCCTT | 55833 |
rs377130607 | in-del | GG/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992664 | ATCGGGCGGAGGGGG[GG/T]GGGCACAAATAGGGA | 55833 |
rs377139235 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953350 | GTGCCATCTGATTGT[C/T]GTGTTGCGAATTTGT | 55833 |
rs377216314 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935391 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 55833 |
rs377291174 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006038 | GAGTTCAAGACCAGC[C/G]TGGCCACCACAGTGA | 55833 |
rs377301559 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008585 | GTCTCAAAAATGTAA[C/T]AAAATCAAAATGCAA | 55833 |
rs377313938 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932770 | CATCCTCATTCCTTA[A/T]CCCCACAGAGCCCAG | 55833 |
rs377338245 | snp | A/C/T | 0.000198051 | 0.00994955 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973278 | ATAAAATAATACTTA[A/C/T]GTCCTACACAATTAC | 55833 |
rs377358049 | snp | C/T | 3.6295e-05 | 0.00425983 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922699 | CACCTGTGCATCCTG[C/T]GGAAGGTGGTGGTGC | 55833 |
rs377364893 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971801 | AAAAGAAGCAAACAC[C/G]TAAGCCAAAATATTA | 55833 |
rs377381704 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000335 | TTTTCAATCACATTA[C/T]TGACTGAAGTTTCGT | 55833 |
rs377388600 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031374 | GGCATGTGTCTGTAA[C/T]CTTGGCTTACTGCAA | 55833 |
rs377405979 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017076 | GTTTCTGTGGTTGCG[C/T]TGATTGTGCTGCTGA | 55833 |
rs377446026 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968455 | CATGTGCAGCCTGGT[A/C]GGCTTCTTCAGCTTC | 55833 |
rs377450987 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934496 | CTTACACCTAGGTCA[C/G]TTCTTACAGAGGCCT | 55833 |
rs377469223 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006238 | GACTCATCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 55833 |
rs377479497 | in-del | -/GG | 0.121717 | 0.214577 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935164 | GCTGTTGGAAGTGGC[-/GG]GGGGGGGGGGTCTCA | 55833 |
rs377494969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014293 | GATAGAGTAACTGCA[C/T]TCTAGACTGGGCTAC | 55833 |
rs377497936 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942269 | GTGAACCAAGATCGC[A/G]CCACTGCACTCCAGC | 55833 |
rs377498874 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962462 | ACCAGCCTGGTCAAT[A/G]TGATGAAACCCCGTC | 55833 |
rs377515994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926263 | AAACTCCAGGGCCAC[A/G]TAAGCAACCTCCATG | 55833 |
rs377548403 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044655 | GGATCACCTGAGGTC[A/T]GGAGTTCCAAGACCA | 55833 |
rs377549866 | snp | A/C/T | 8.24659e-05 | 0.00642082 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923779 | GAGACACAGTCACAC[A/C/T]CTCTGAAATACTCAC | 55833 |
rs377553213 | snp | C/T | 1.76166e-05 | 0.00296783 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948338 | AAGCTTGAAACGTCC[C/T]CAGTAGGGGCAAACC | 55833 |
rs377554962 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978452 | TGTACTATATAGACC[A/G]TATTCATGCAATAAT | 55833 |
rs377556391 | snp | C/T | 9.96115e-05 | 0.00705662 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998763 | AGATTATAAAAATGA[C/T]GATATCCTTTGCCAG | 55833 |
rs377589509 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003595 | TATTTTTAGTACAGA[C/T]GCGGTTTCACCATGT | 55833 |
rs377620358 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998095 | ACTTTTCCAACAAGA[A/G]TATGAAATCACAACC | 55833 |
rs377643460 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003283 | TGATCTGCCCACCTT[A/G]GCCACCCAAAGTGCT | 55833 |
rs377647920 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991439 | GGCTACATACTGCTC[A/C]ATTTATGGATACACT | 55833 |
rs377732672 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024986 | AGACTCTGTCTCCCC[-/A]AAAAAAAAAAAACTT | 55833 |
rs377761353 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925818 | TTCCTCCAGCAACAG[C/G]AAAGACTGTATCCAG | 55833 |
rs386414856 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936927 | GCAAAACTCCAGCTC[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs386414858 | in-del | -/CAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945505 | GACAAACAAACAAAC[-/CAAA]AAAAAACAAAATCCA | 55833 |
rs386414859 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961545 | TACTCAAAAAATACT[-/T]TACTTACAGATCTTA | 55833 |
rs386414860 | in-del | -/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961546 | ACTCAAAAAATACTT[-/T]ACTTACAGATCTTAT | 55833 |
rs386414861 | in-del | -/TTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011997 | ACCAAAGATAAACAT[-/TTA]TAACAGTCTACTAAG | 55833 |
rs386414862 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018876 | CAAAATAAATAAATA[-/AAAA]AATTTTAAAAATAAA | 55833 |
rs386414863 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039848 | GATCAATAAATACTA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs386734391 | multinucleotide-polymorphism | AC/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925370 | CACAGAACACGAGAA[AC/TT]CTCCAGGCAGGAACT | 55833 |
rs386734392 | in-del | ACAA/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942433 | AAAACTAAAACAACA[ACAA/G]CAACAAAGTCAGCCA | 55833 |
rs386734393 | in-del | AGG/GC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992658 | CAACTTATCGGGCGG[AGG/GC]GGGGGGGGCACAAAT | 55833 |
rs397688134 | in-del | -/TTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011999 | CAAAGATAAACATTA[-/TTA]ACAGTCTACTAAGCC | 55833 |
rs397696939 | in-del | -/A | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043845 | CAGGGGGAAAAAAAA[-/A]GGCCAGGCACAGTGG | 55833 |
rs397700818 | in-del | -/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020677 | TCCTTTTTTTTTTTT[-/T]GAGACAGAGTCTGGC | 55833 |
rs397713883 | in-del | -/AC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019724 | CACACACACACACAC[-/AC]GCACAGAAAAACATG | 55833 |
rs397715137 | in-del | -/CAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945508 | AAACAAACAAACAAA[-/CAAA]AAACAAAATCCAATA | 55833 |
rs397716667 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029276 | TCAGACCTGTAATCC[-/C]AGCACTTTGGGAGGC | 55833 |
rs397725928 | in-del | -/TTTTTT | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990653 | TTTTTTTTTTTTTTT[-/TTTTTT]GAGACAGAGTCTCAC | 55833 |
rs397729108 | in-del | -/A | 0.375 | 0.216506 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943075 | TTTCATTGTGTTGAT[-/A]ATACCACATTTTATT | 55833 |
rs397740386 | in-del | -/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035907 | CTCTCTTTTTTTTTT[-/T]GAGTGGGGGAAATCG | 55833 |
rs397755438 | in-del | -/A | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041315 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 55833 |
rs397760286 | in-del | -/A | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012541 | TCAAAAAAAAAAAAA[-/A]GGCATTATGAGGACC | 55833 |
rs397763786 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008336 | AAAAAAAAAAAAAAA[-/A]GTGGGACACAGAAAA | 55833 |
rs397804848 | in-del | -/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018246 | TTTTTTTTTTTTTTT[-/T]AGACAGAAGAGCCGG | 55833 |
rs397807614 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970586 | AGGTGCACACCACCA[-/A]TGCCATGCTAATTTT | 55833 |
rs397830303 | in-del | -/T | 0.375 | 0.216506 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938813 | ATTTCAATGACAAGC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs397893281 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958427 | ACCCCCTTTTTTTTT[-/T]GAGATGGAGTTTCAT | 55833 |
rs397893460 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984519 | AAAATTTTTTTTTTT[-/T]CTTTAAATTAGCCAG | 55833 |
rs397893554 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022454 | TTTTTTTTTTTTTTT[-/T]TAAGACACAGTCTGG | 55833 |
rs397893960 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046314 | TTAAAAAAAAAAAAA[-/A]GAGGACTGGGAAATC | 55833 |
rs397894089 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948002 | AAAAAAAAAAAAAAA[-/A]AGTCTTAAAATGTTT | 55833 |
rs397894157 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956943 | AGGAAAAAAAAAAAA[-/A]TTGGCTGGTCGTGGT | 55833 |
rs397894174 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945154 | TTAAAAAAAAAAAAA[-/A]CTTATTAAGTTTTTG | 55833 |
rs397894322 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935174 | GTGGCGGGGGGGGGG[-/G]GTCTCATTTTCTCCC | 55833 |
rs397935793 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024356 | CAAAAAAAAAAAAAA[-/A]TAGCAAATACATTCT | 55833 |
rs397959453 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017030 | GGAAAAAAAAAAAAA[-/A]GAGTTCCACAAAAAC | 55833 |
rs397962243 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959165 | TCAAAAAAAAAAAAA[-/A]TTAAAGTACTTATTT | 55833 |
rs398010658 | in-del | -/TTTT | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013174 | ATCTCCTTTAACCTC[-/TTTT]TTTTTTTTTTTTTTT | 55833 |
rs398010660 | in-del | -/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024356 | AGAATGTATTTGCTA[-/T]TTTTTTTTTTTTTGA | 55833 |
rs398040336 | in-del | -/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984693 | ATCCTTTGTCTACTG[-/T]TTTTTTTTTCTCTTA | 55833 |
rs398046539 | in-del | -/T | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969096 | ACATTTGAGGTTTTT[-/T]CCCCCCAGACAGACC | 55833 |
rs398046540 | in-del | -/A | 0.5 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041314 | AAAAAAAAAAAAAAA[-/A]ATTAGCCAGGCATGG | 55833 |
rs398073485 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990654 | TTTTTTTTTTTTTTG[-/TTT]AGACAGAGTCTCACT | 55833 |
rs398087268 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956942 | TAGGAAAAAAAAAAA[-/A]ATTGGCTGGTCGTGG | 55833 |
rs398087269 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990652 | TTTTTTTTTTTTTTT[-/TTT]TGAGACAGAGTCTCA | 55833 |
rs398087270 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035906 | TCTCTCTTTTTTTTT[-/T]TGAGTGGGGGAAATC | 55833 |
rs527247371 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990263 | ACTGTTTTATGCTTT[C/T]TAAAAATCTTACAGA | 55833 |
rs527248867 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019495 | ACAAGTAGAATGGTA[A/G]TTACCAGAGGCTGGG | 55833 |
rs527257110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046601 | GTGAGCCGAGATCAG[A/G]CCACTGCACTCCAGC | 55833 |
rs527270074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002711 | AGGGTTTCATTGTGT[C/T]GGCTAGGCTGGAGTG | 55833 |
rs527284131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008901 | ACCCACAAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 55833 |
rs527302916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960554 | GTTGAGGCGGGTGTA[G/T]CACCTGAGGTCAGGA | 55833 |
rs527306680 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016563 | TTTTTATTTATTTTA[-/T]TTTTTTTTTTAGGAA | 55833 |
rs527379675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955293 | TAGGAGGCCGAGGCT[A/G]GCGGATCACGAGGTC | 55833 |
rs527385324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047287 | AAGCAAAAGGGCAGT[C/T]TGGGAAACTAATCAC | 55833 |
rs527413029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003448 | GTGATCGCGACTCAC[C/T]GCAACCTCCGCCTCC | 55833 |
rs527416024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954526 | TTGTAATGAATGCCA[C/T]TGAATCCTTTCAAAG | 55833 |
rs527452386 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943761 | AGAGAAAGAAAAAAA[A/G]CAAGCTAAGAAAAAT | 55833 |
rs527490314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948067 | AGAGAGCTCAGAAAA[C/T]TCTGTCCATGCATTT | 55833 |
rs527490375 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964435 | GAAAGAGAAAATTTT[-/A]AAAAAAAGTAACTAA | 55833 |
rs527516030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996409 | TTCTTCTATACAAAT[A/C]CAGAATTACATAATC | 55833 |
rs527517569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035220 | TCAAAACATTTCATA[C/T]GGCTAGGCGCGGTGG | 55833 |
rs527535474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029922 | AACCCGAGAGGCAGA[G/T]GTTGCAGTGAGCTGA | 55833 |
rs527537798 | in-del | -/GTAT | 0.241053 | 0.24984 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999854 | AGCTGGGATTACTAC[-/GTAT]GTATGTATGTATGTA | 55833 |
rs527551342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977005 | TGACAAAGTAAGACT[C/T]GGTCTTGGAAAAAAC | 55833 |
rs527565428 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983413 | AAGCATGTGAGAGAT[A/C]AAATACCCTAGGAAA | 55833 |
rs527565817 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967160 | ATTTTTTTCCATTTT[C/G]TGTTTGTTGATGATT | 55833 |
rs527591038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982927 | CACTGTCACCCAGGC[C/T]GGAGTGCCATGGCAT | 55833 |
rs527600115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989490 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCACATGC | 55833 |
rs527607742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029311 | GAGGGTGGATCACCA[A/G]AAGGTCAAGAGTTTG | 55833 |
rs527644155 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044820 | GCAGTGGGCGAAGAT[C/T]GTACCACTGCACTCC | 55833 |
rs527682243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994259 | CCAAAGGAGGAGGGG[C/G]TGTTAAAACTCAAAA | 55833 |
rs527683592 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986941 | AATGACAAACAGGCT[A/G]CAATTTAAACAACGG | 55833 |
rs527695194 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002070 | CAAGCACTCCTCTGA[A/C]CTCAGCCTCCTGAGT | 55833 |
rs527704903 | snp | A/T | 1.66432e-05 | 0.00288467 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953478 | ACCAGATCAATGCTA[A/T]GCAGACAAAAAGCAA | 55833 |
rs527710913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039282 | AGAGGTGGGGGGGGC[A/G]CCTCTGCCCGGCCAC | 55833 |
rs527773700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046418 | ACTTTGGGAGGCAGG[C/T]GGATCACGGGGTCAG | 55833 |
rs527780253 | snp | A/G/T | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921408 | CCTGCCCTGGTATCC[A/G/T]GTGGACAGGGCTCTG | 55833 |
rs527794715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987365 | TGCAGTGAGCCGAGA[C/T]CTCCTCACTGCACTC | 55833 |
rs527795092 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946249 | TATTAAGGAAATTAA[C/T]TCTTTTTGTCTATGA | 55833 |
rs527851503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925598 | TTTGGGCCTTTGGCC[A/G]GCAGATTAAAGGGCT | 55833 |
rs527856775 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000381 | CCAACAAAAAATCAG[A/C]AAAGTTCTAAAGAAA | 55833 |
rs527859735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022654 | ATGTTGGCCAGGCTG[A/G]TCTTGAACTCCTGAC | 55833 |
rs527886472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931405 | GGAATACATGGTCTG[A/G]AGGTTTTTTTTTGAG | 55833 |
rs527919383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028541 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 55833 |
rs527971519 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024101 | CGGTGGCACACGCCT[C/G]TAATCCCAGCATTTT | 55833 |
rs528019482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968430 | GGGCATACATAGTCA[C/T]GGCCGAGGGCATGTG | 55833 |
rs528040821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975846 | CAGCTACTATGGGTA[A/G]CAGTATGGCAGTTCC | 55833 |
rs528056483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934538 | GCAGTCTCTTCCATA[C/T]ATAAACCTTGTTCAT | 55833 |
rs528084139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984056 | CTACAGGCACACACC[A/G]CCATGCCCAGCTAAT | 55833 |
rs528099730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950152 | CTCACTGCAAGCTCC[C/G]CCTCCCAGGTTCACT | 55833 |
rs528110968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037120 | CGGCCTCCGGATTAG[C/T]TGAGATTACAGAGGC | 55833 |
rs528126196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030380 | CGTGAACCCGGAAGG[C/T]GGAGGTTGCAGTGAG | 55833 |
rs528158020 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955799 | GCCACTGCACTCTAG[C/G]CTGGGCAACAAGAGC | 55833 |
rs528182567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984681 | AGACACTGTCTCTTA[A/G]GAGAAAAAAAAACAG | 55833 |
rs528196220 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030705 | GCCCGGGCGCATGGA[A/T]CACAAGGTCAGGTGA | 55833 |
rs528221288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970934 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAGGCAT | 55833 |
rs528244819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929090 | AGCCCCACCAGGAGC[A/G]GGCCAAAGGATGCAC | 55833 |
rs528255309 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019711 | CACACACACACACAC[A/G]CACACACACACACGC | 55833 |
rs528273844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012595 | TGTAGATGTTCTGAT[G/T]TTTTATAATTGTACT | 55833 |
rs528278341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972310 | AAATATTACCTTTAA[A/C]ATTTTCACAAAGGAA | 55833 |
rs528278354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979500 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 55833 |
rs528346259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013095 | GGAGGCACAGTTGCC[A/G]TTAGCCGAGATCAAG | 55833 |
rs528439107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973030 | TAAAAGATCAATTTT[A/G]TTCATATTATTTTTC | 55833 |
rs528454349 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977434 | CTCACCTGGTAGTAA[C/T]GCTACTAGTAACATT | 55833 |
rs528458375 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961252 | GGTTTGATTTCTTCC[A/G]ATATAGTCTTCAAAA | 55833 |
rs528465040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927516 | GTCGTGGAGCCCACC[A/G]TAAGTCATCCCTGGC | 55833 |
rs528482457 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957562 | TTATTTTGGGATATA[C/T]GCACACTGTTTTAAC | 55833 |
rs528483811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933312 | GCAGGCAAGGTTTCC[A/T]TATCTGGTGGTTTTA | 55833 |
rs528484203 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000988 | TAAGGACCTTACATA[C/T]ACTCTCACTATCCCT | 55833 |
rs528528061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971248 | AGGCAACGTTGCTAC[A/C]AACCCATCTATCATC | 55833 |
rs528535534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024121 | CCCAGCATTTTGGGA[G/T]GCCGAGCCGGCTGGA | 55833 |
rs528543168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962416 | ACTTTGGGAGGCCGA[A/G]GTGGGTGGATCACGA | 55833 |
rs528544035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018109 | GGAAGACTGCTTGAG[C/G]CCAAGAGTTTGAGAC | 55833 |
rs528553139 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010694 | GTGGGGAGGGATTTT[C/G]GCAGACAGAAAAGGA | 55833 |
rs528564194 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985852 | CATGGTAAAACCCCA[C/T]GTCTAGCAAAAATAC | 55833 |
rs528573989 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048379 | TTAGAGAGCGCATAA[C/G]TTGGGGCTATAACAG | 55833 |
rs528666741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004279 | TTTGGTGTAATTTTT[A/T]TTTCTTAGCTCACTA | 55833 |
rs528666769 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942570 | CTGTCTCTACAAAAC[-/AT]ATTTAAAAATTAGCT | 55833 |
rs528682089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011134 | GTGAAAGAATCTCAC[C/G]AAATATTTCAAGCAG | 55833 |
rs528698661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963072 | ATTAAACACAACTTT[A/G]GACTTGCATAATAGG | 55833 |
rs528740968 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921963 | GGGTGGAGGGATACC[A/G]CTGCTATTCCCAGAT | 55833 |
rs528789117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998129 | TTTGAAATGGCAATT[A/C]AGGCCAGTAATCCTG | 55833 |
rs528793962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043131 | TTATACAATGACAAC[G/T]CTACATGTTTTTATG | 55833 |
rs528814907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956380 | AAGGAGTGCAGTGAC[A/G]TGATCTCGGCTCACT | 55833 |
rs528841457 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033878 | GTAGCTGGGATTACA[A/G]GCACCCACCACCATG | 55833 |
rs528872483 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004645 | AAAAATTAGCCGAGC[A/C/G]TGGTGGCGGGCACCT | 55833 |
rs528881807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989545 | CACAGCTTGCAGCTC[A/G]CCTGCTTATCATTTA | 55833 |
rs528884026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036037 | AAAATAACAGCAAAT[A/T]CTAATAAAACTAAAC | 55833 |
rs528909012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042284 | GAGTTTGAGACCAGC[C/T]TGGCCAACACAGTGA | 55833 |
rs528914480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956290 | AATATACAAGTGACC[A/G]TGACAAGTAATTTTC | 55833 |
rs528968979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030113 | CAAGACCAGCCTGGG[C/G]AACATAGAGAGAACC | 55833 |
rs528970391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984008 | CCTCCACTTCCCCCA[A/G]TTCTCGTGCCTCAGC | 55833 |
rs528970607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036369 | TGATCTGCCCGTCTC[A/G]GCCTCCCAAAGTGCT | 55833 |
rs528991331 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990613 | TAACCTTTCTAGAAG[G/T]TTACTTAGAAATAGT | 55833 |
rs529017884 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940979 | TCCAAGGTATGCCTG[C/T]AGTGTCATCCATATT | 55833 |
rs529027024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934919 | ATGTCAAACCAAAAT[C/G]CTGGGGCTCCAAATC | 55833 |
rs529028371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928065 | GAGAGCCTGGCCTGG[C/T]GCTTGGGCCCAAGTC | 55833 |
rs529041011 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965600 | AAGTGTAACCTTGGA[A/G]GGTAATTTTTGTATA | 55833 |
rs529059203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025384 | CTAAAAATAATCCAG[A/T]AGAAACTCAAACATA | 55833 |
rs529059959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018350 | GTTTAATTTTAAAAA[C/T]ACAGAAAGCATCGGT | 55833 |
rs529070885 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986280 | GCAGGGTCTCAAAAA[A/C]AGGGAATAAGTTCTA | 55833 |
rs529096286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030694 | CACTTTGGGAGGCCC[A/G]GGCGCATGGATCACA | 55833 |
rs529138855 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018841 | GCGCTCCAGCCTGGG[A/C]AACAGAGCAAGACTC | 55833 |
rs529140954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972061 | TCAAGGCAGAATAAG[A/C]GCTCTTATGAGAGTC | 55833 |
rs529165571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011452 | TTAACAATAACAATA[C/T]AGTAACACTAGTGCT | 55833 |
rs529175506 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922295 | TCTGCCGCCATCCCC[C/G]AACTCCCCCCCAGAC | 55833 |
rs529184403 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001568 | TCCCTGGGCAAGCGG[C/T]TTGTGCCCCAAGCAC | 55833 |
rs529230539 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954594 | CATGCCAATAAGACA[A/G]GCAGATTACAGGACA | 55833 |
rs529232738 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036347 | GTCTCAAACTCCCGA[C/T]CTCAGGTGATCTGCC | 55833 |
rs529261072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976047 | AAAGCGAGATGCCAC[C/T]TCTACAATAAATTTT | 55833 |
rs529268054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023599 | CTATAAATAATGACC[C/T]GGTTGCATGGCTAAA | 55833 |
rs529269776 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990144 | TATCAAGCAGGGTAG[C/T]TACAGAGAAATCCTA | 55833 |
rs529275620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988918 | GGGAGGCTGAGGCGG[A/G]AGGGTCACTTGAGAT | 55833 |
rs529277401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932703 | ACGCACGTGGGTCAG[C/T]GAGCTAGATTCAAAC | 55833 |
rs529282335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940087 | AAGAAAAAGAAGAAA[A/G]AAAGGAGGAGGAGGA | 55833 |
rs529332168 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942319 | TGTCTAGAAAAAAAG[-/A]AAAAAAAATAAGAAG | 55833 |
rs529332519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977375 | AAAAATCTAATCCAT[C/T]GTCCCCATAAATTCT | 55833 |
rs529380567 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963309 | ACATTAAATACAGAA[-/G]GCAAAGGCTCAGGTC | 55833 |
rs529393516 | snp | C/T | 0.000187984 | 0.00969313 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926942 | CCAGGTGCCAGCCCC[C/T]GAGGCCAGGGGAGCT | 55833 |
rs529425027 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974055 | ACAAAACTATTTTTA[-/T]TGGGCATGTGCCTCT | 55833 |
rs529434363 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003646 | TCCTGACCTTAAATG[A/T]CCCTCCTGCCTTGCC | 55833 |
rs529436317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010555 | TTAAAAACTTAGATA[A/G]AATAATGGCTGGCTA | 55833 |
rs529451447 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040956 | TAAAAGTTACACATA[C/G]CCTACATACAAACCA | 55833 |
rs529480903 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009081 | TTCCAAAATAATTTT[C/T]CCCTAAAAATTTGGT | 55833 |
rs529560806 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041516 | GCCTGGCCAACATGG[-/T]TGAAACCCCGTCTCT | 55833 |
rs529566492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955732 | CTGGGAGGCTTGAGG[A/C]AGGAGAATCACTTGA | 55833 |
rs529597337 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021403 | CTCCAGTCAGTATGA[A/G]TACACATTTTGCATC | 55833 |
rs529601002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048263 | AACCAGACTACAGGA[A/G]CGGCGGGTGTGGAGG | 55833 |
rs529638246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020483 | GCACGCGCCACCATG[C/T]CCGGCTAATTTTTGG | 55833 |
rs529654223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955464 | GGCGGGGGTTGCAGT[C/G]AGCCGAGATCGTGCC | 55833 |
rs529659087 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972873 | TCAGGCGAAGTGCTA[C/T]TGACATTTATTAATA | 55833 |
rs529700627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936396 | TCTCCCAGGTTCAAG[C/T]GATTCTCCTACCTCA | 55833 |
rs529713971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966253 | AAGAGTTCAATACTT[A/G]CCTGCCCAACATGGT | 55833 |
rs529721674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013898 | AAAAAGAAAGAAAAA[A/G]ATTGCCAAATAAAGC | 55833 |
rs529723912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929229 | CAACCTTTTAATCTC[A/G]GAAGGAAAAATGAAC | 55833 |
rs529735371 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975751 | AGCTTGCAGTGAGCC[A/G]AGATCACAACACTGC | 55833 |
rs529754194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026953 | GGCATCACCTGCAAA[G/T]CTTGTGCCTGATGAC | 55833 |
rs529755695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974387 | TGGTACATGCCTGTA[G/T]TCCCAACTACTCGGA | 55833 |
rs529756364 | in-del | -/T | 0.0704347 | 0.173943 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984509 | CTCTTAAAAAAAAAA[-/T]TTTTTTTTTTCTTTA | 55833 |
rs529778337 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949576 | GGGATGGTGGTGAAC[A/G]CCTGCAATCCCAGCT | 55833 |
rs529797071 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | UBAP2 | GRCh38.p7 | 9:33924277 | GCAAAGGGAATTCCA[C/T]AGTAGTCCTAGGAGA | 55833 |
rs529797800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973686 | AAGCATGAGAACAAG[A/C]AAGCAAGAAGAGAAA | 55833 |
rs529802571 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973689 | CATGAGAACAAGCAA[A/G]CAAGAAGAGAAAATT | 55833 |
rs529859256 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001628 | TCTAAATTTAGTTGG[G/T]TATGACAAGATAACT | 55833 |
rs529918331 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049556 | CTCGCTCTGCGCCCT[C/G]CCCCCTGCGCGGGAA | 55833 |
rs529935368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038967 | AGCGCCTCTGCCCGA[C/G]CGCGACCCCGTCTGG | 55833 |
rs529946359 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927441 | GCTGAGTTCGAAGTC[A/G]GTTTTAGCAGCGACC | 55833 |
rs529954773 | in-del | -/CTTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036806 | ACCTTAAGTTTTTCT[-/CTTTT]TTTTTTTTTTTTTTT | 55833 |
rs529998343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924419 | AGCAGTCCCAGGGAA[C/T]GCCAAGTAAATGGTG | 55833 |
rs530007904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008090 | TAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 55833 |
rs530010349 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049560 | CTCTGCGCCCTGCCC[A/C]CTGCGCGGGAAAACG | 55833 |
rs530021792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964244 | TGGACTCATAACTCT[C/T]TTATCAACAAGCCAA | 55833 |
rs530044158 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046658 | AAAAAAAAAAAAAAA[-/A]AAAAAAAAAAAAAAG | 55833 |
rs530049999 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958977 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 55833 |
rs530071499 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930509 | CATGGAAACATCAAG[A/G]TACACTTGTGGGGAT | 55833 |
rs530091589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950504 | TGGAAATCCTAACTT[C/T]GCTTTGAGTAAAACA | 55833 |
rs530103905 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012996 | CCCTCTCTACTAAAA[C/G]TACTAAAATTAGCCG | 55833 |
rs530116897 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005147 | ACGAGCCTGAAATCC[C/T]AACTACTCAGGAGGT | 55833 |
rs530125761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044006 | GGTGGCAGGCTAATC[A/G]CTTGAACCCAGTAGG | 55833 |
rs530145611 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050180 | CGTGTTAACAAGCTC[C/T]CAAGGTCCTCTAAAC | 55833 |
rs530175070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957230 | CCATGAGTTTCTATT[A/G]TTTTTAAAAAATTAA | 55833 |
rs530229216 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946714 | AACAGAATTTAATTT[-/A]AAAAAAAAACAAATG | 55833 |
rs530240388 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999027 | ATATAACCTGTTCCC[A/C/G]TAGGAAAAATAAGCA | 55833 |
rs530245717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005887 | GTCCTTGAGAATATC[A/G]ATCCCTAAATAATCA | 55833 |
rs530256560 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037930 | CAACACTTTGGGAGG[C/G]TGAGGTGAGCACTTG | 55833 |
rs530302030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979710 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 55833 |
rs530324249 | snp | A/C | 0.000340017 | 0.0130343 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935735 | GGCTGCTTTTTAACG[A/C]ATAAGCCATTGACCA | 55833 |
rs530332712 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980488 | CCTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 55833 |
rs530349243 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957713 | CTAATGAGGTAACAC[A/G]GAAAACATAAAAATG | 55833 |
rs530356672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943186 | CACATATTCCAAGAT[C/T]CCAGTTATATGAAAT | 55833 |
rs530368282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032078 | TGATCCCAGGATTTC[A/G]AGGCTACAGTGAGCT | 55833 |
rs530393207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976681 | GGATGAAATGTATGG[C/T]ATGTAAATTTTGTAA | 55833 |
rs530413239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943896 | ACACGGCGAGACCCT[A/G]TCTCATTTAAAAAAA | 55833 |
rs530429427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031542 | AAACTCCTGACCTCA[A/G]GTGATCCACCCGCCT | 55833 |
rs530434274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992715 | ATCTTTACAATACCA[C/T]AGTAACTGCTAAAAA | 55833 |
rs530438384 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038417 | CCTGCCAAGTGCCTG[A/C/T]GATTGCAGGCGCGCG | 55833 |
rs530451019 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984839 | CTATTATCAAAAAGA[A/C]AAAAAATAGCCTGTA | 55833 |
rs530483675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019884 | AACAAATGTGCAGCC[A/G]GTCGCGGTGGCTCAT | 55833 |
rs530490659 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973118 | AGATGTAGGGTATTA[A/G]AAGCAACTGCAGAAT | 55833 |
rs530500207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928846 | TATAAACTCGTAGAA[A/G]AAAAGCCAAAGAACG | 55833 |
rs530505215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002789 | ATCCTCCCACCTCAC[A/G]CACTCCACCCCCCAT | 55833 |
rs530514675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978796 | AAAAAAAGAAAGAAA[C/G]AAAGAAAAAGTAGAG | 55833 |
rs530525399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979590 | TCAAAAAATAAAAAT[A/G]AAAAATAACTGGCCA | 55833 |
rs530533314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943112 | GCAATAAAAATGATA[C/T]ATTAAACATGGGTGT | 55833 |
rs530569110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025598 | AAGCTTCCTATTAAC[A/G]ATTAAAGTGAAAAAA | 55833 |
rs530580172 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030722 | ACAAGGTCAGGTGAT[C/T]GAGACCATCCTGACT | 55833 |
rs530604892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013679 | GTCAGAAGTTTGAAA[C/G]CAGCCTGGCCAACAC | 55833 |
rs530664937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020318 | TGATAACAATGCAGA[A/G]CCAATGATTTTTTTT | 55833 |
rs530664978 | snp | A/C | 0.483708 | 0.088773 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013152 | AGTGAGACTCTAGCT[A/C]AAAAAAAAAAAAAAA | 55833 |
rs530699233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965263 | CTTCTTCCATTTTTT[C/T]CCCCCATTTTTAATT | 55833 |
rs530718324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006102 | GCCGGGCATGGTGGC[A/G]TGCACCTGTAATCCC | 55833 |
rs530775714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958324 | ACTTACAAATTAAAT[C/T]GATTTACGAAAAAGA | 55833 |
rs530793154 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971327 | GGGAAGTACTTCCAG[C/T]AAAAAATCTTCTCCT | 55833 |
rs530851678 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932173 | CTCGGCAGTGCATGT[C/T]TGCTTCCACTCCTGC | 55833 |
rs530865061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966227 | CTGAGGTGGGCAGAT[C/T]ACTTGAGGTCAAGAG | 55833 |
rs530865113 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957680 | GGACTCGGCTTTGAA[A/C]GGCTGGAAAATGTTG | 55833 |
rs530915500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011241 | ACTGTTTCACCCATA[A/C]ATTTCTAACTATAAA | 55833 |
rs530951251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963532 | TAATGATGAAAATTC[A/T]GTGGCACCTTGAAAG | 55833 |
rs530957104 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008306 | GTGGGCAACAAGAGC[A/G]AAACTCCGTCTCAAA | 55833 |
rs530973520 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921432 | GGCTCTGTGGGACAC[C/T]GCCCTATCCCTAAGT | 55833 |
rs530975009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018260 | TTAGACAGAAGAGCC[A/G]GGAATTTTCCGATAA | 55833 |
rs530999717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012360 | ACATGGCGAAACCTC[A/G]TTTCTACTGAAAATA | 55833 |
rs531022527 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005132 | GCAGTGCGTGGTGGC[A/G]CGAGCCTGAAATCCC | 55833 |
rs531033513 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961254 | TTTGATTTCTTCCGA[C/T]ATAGTCTTCAAAACA | 55833 |
rs531100433 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960696 | GAGGCAGAAGAACTG[C/T]TTGAATCTGGGAGGC | 55833 |
rs531124731 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991400 | GGATTCCCAAAATAT[C/T]AAATTCAGGAGACTA | 55833 |
rs531135495 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950326 | TCCACCTGCCTCAGC[C/G]TCCCAAAGTGCTGGG | 55833 |
rs531146029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998333 | AGCCTAGGAGTTTGA[C/G]GCTGCAGTGAACTAT | 55833 |
rs531159470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043284 | TTAAGCAATCCTCCA[A/C]CCTCAGCCTCCTGAG | 55833 |
rs531159904 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938717 | AGGAGAATCGCTTGA[A/G]CCCGGGAGGTGGAGG | 55833 |
rs531189924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968331 | GATGCCCATGTTCAT[C/T]GGTCACAGAGCCAAC | 55833 |
rs531218783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942297 | AGCCTGGCGACAGAG[C/G]AAGACTCTGTCTAGA | 55833 |
rs531225075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037822 | AAAAATACTTCAGTG[A/C]CAATATGTAAATACA | 55833 |
rs531249665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037249 | CGCCTCGGCCCCCCA[A/G]AGTGCTGGGATTACA | 55833 |
rs531257542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960501 | CAGGTATCGGCCAGG[C/T]GCAGTGTCTCACGCC | 55833 |
rs531291468 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022146 | ACTACTTAGGAGGCT[A/G]AGGCAGGAGAATCGC | 55833 |
rs531322723 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008312 | AACAAGAGCGAAACT[C/T]CGTCTCAAAAAAAAA | 55833 |
rs531331768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002163 | CTCACTGTGTTGCCC[A/G]TGCTGGTCTCAAACT | 55833 |
rs531348249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959860 | CACAAATCTGGGCAA[C/G]AGTGTCAGCTGGCTA | 55833 |
rs531377695 | in-del | -/TAATT | 0.454302 | 0.144085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995556 | AAATATATTATTAAA[-/TAATT]TAATTTAATTTAAAA | 55833 |
rs531384887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925457 | ATCTCAAAAGGTGGG[C/T]TCCAGAGGGTGTTTT | 55833 |
rs531408757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008794 | ACATGGTGAAACCCC[A/G]TCTCTACTGAAAAAA | 55833 |
rs531418254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954507 | TGCACCGTATTACCT[A/G]ACCTTGTAATGAATG | 55833 |
rs531421921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945655 | ATATCACAATATATA[C/T]AGACAGACAGACAGA | 55833 |
rs531424951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039449 | TAGAGAAATCAGATT[A/G]TTGCTGTGTTTGTGT | 55833 |
rs531435682 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949123 | AGTGAGCAGAGATCA[C/T]GCCACTGCACTACAG | 55833 |
rs531454604 | in-del | -/AAAATACAAA | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987430 | AAAAATACAACATAC[-/AAAATACAAA]AAAATACAAAAATTA | 55833 |
rs531497057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947861 | ATAGAGTAAAATATT[A/G]TCTAGGCTGGATACA | 55833 |
rs531515653 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988365 | CATTTTATTCTTTCA[A/T]AACTTAGCTACACTG | 55833 |
rs531561281 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040142 | CTAGCCTGGGCGACA[A/G]GGGCTAGACTCCGTC | 55833 |
rs531593141 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028678 | AGCCACTGCGACCAG[A/C]CTTAAACCTTGTCTT | 55833 |
rs531619699 | in-del | -/TCT | 0.000148391 | 0.00861241 | cds-indel | UBAP2 | GRCh38.p7 | 9:33960827 | CAGCAAACACTTACA[-/TCT]TCAGTCCAGTCTTCT | 55833 |
rs531623799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33952120 | ACAAACGATTTGACT[C/T]GGGAGAAAATTCTGT | 55833 |
rs531655112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034474 | ATTTAAACATTAACA[C/T]ACCTGCCACATAAGT | 55833 |
rs531688466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992937 | ACAGCAGTCTTCGAA[C/G]CCAGCTAGTTCAAAA | 55833 |
rs531690756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936621 | TGTACTCCAGCATGG[A/G]CAACAGAGCAACACT | 55833 |
rs531693350 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024621 | ATCTTCTGGAAAAAC[A/G]GGTCAGAAAATAACT | 55833 |
rs531710220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038824 | CCTGGCCGCCATCCC[A/G]TCTAGGAAGTGAGGA | 55833 |
rs531711289 | in-del | -/TATAATCTCCTAATATC | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970182 | CAAGCTGAGTTATCT[-/TATAATCTCCTAATATC]TATATGATCCATATC | 55833 |
rs531730380 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925116 | CTGACCTGACCCTCA[C/T]TCACCATCCAGGGCC | 55833 |
rs531781183 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042178 | CATATAAGGTAAAAT[C/T]ATTGTAAAAAAGTAA | 55833 |
rs531789479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021443 | TTTAACAACTTTATA[A/C]TTTTGTTGGTTTGGG | 55833 |
rs531792812 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013505 | TCAAAAAATAAAAAA[-/CT]CTCTTTCATCATGCA | 55833 |
rs531801006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980783 | CAACATGGCAAAACC[A/C]TCTCTCTACAAAAAT | 55833 |
rs531837286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026864 | TGCTATGTTGTAAGG[C/T]TAACTGTTCAGTCAC | 55833 |
rs531852324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967224 | TTGCATCTTGTGCTT[A/G]TGAAACTCTCCAATA | 55833 |
rs531855866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986394 | AAGACTACAACTCAC[C/T]GAAAGCTCAAATGAT | 55833 |
rs531897072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925084 | AGCACAGTGGAGCTT[C/T]GTGGAGGAGGGGAGG | 55833 |
rs531913567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974564 | GGCAACCCAAAGAAT[C/G]GAAGAAAATATTTAT | 55833 |
rs531934461 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942440 | AAACAACAACAACAA[A/C]AAAGTCAGCCAGGCC | 55833 |
rs531953923 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977288 | GTGATCCGCCCGCCT[C/T]AGCCTCCCAAAGTGC | 55833 |
rs531965027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974496 | AGTGTGACAGAGTGA[C/G]ACCATTTCTCAAAAA | 55833 |
rs531994251 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014456 | CAACATGGTGAAACC[A/C]TGTCTCTACTAAAAA | 55833 |
rs531995490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975301 | GCCAGGCGTGGTGGC[A/G]CGCGCCAGTAGTCTC | 55833 |
rs532008634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014618 | TGGGCGACAGAAGGA[A/G]ACTCCATCTCGAAGA | 55833 |
rs532040698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968166 | CAATGAATAGAAGAA[G/T]AAATCTACTGGGTTT | 55833 |
rs532062944 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971140 | ATCTCAATAATTACT[A/G]TACAAAGAACTCTAT | 55833 |
rs532085882 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000113 | TCACTGCACCCAGCC[A/G]TATTTATTTAATTTT | 55833 |
rs532101490 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924998 | AAGGAAGCCAAAACA[C/T]TGGACACCCCTGGCC | 55833 |
rs532110740 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926007 | CCAGGAAAGGCCCAC[A/G]CTGCATTCTGGCACC | 55833 |
rs532123564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966994 | TAAATGTCACAACAG[C/T]GGGACTAAAATATAT | 55833 |
rs532183165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001540 | TCATTGTGGCAGCTG[C/G]CCTGCAATATAATCC | 55833 |
rs532191543 | in-del | -/G/GT | -0.997204 | 1.41174 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994712 | TGTCTTGTGTACCAG[-/G/GT]TGTTCTCTTACATGG | 55833 |
rs532217524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015071 | GGTATAAATGAGTGA[C/T]TTTAAGAAGCACTTT | 55833 |
rs532227975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045369 | AGGGTAGAAAAAAAT[A/G]AAAATTAAAAAAAAA | 55833 |
rs532242559 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927197 | GGGTTCAAAGAAGGG[C/T]AGTGGCCGAATGAGG | 55833 |
rs532272055 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950780 | GCTTTACAACACAGC[A/G]AAATCACTGAATCAA | 55833 |
rs532299117 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033908 | GCCTGGCTAATTTTT[C/G]CATTTTTAGTAGAGA | 55833 |
rs532299215 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952351 | GCCTATCTTCACAGC[C/T]TTCACTAACAGTTTC | 55833 |
rs532342009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008252 | GAACCCAAGAGGCGA[A/G]GGTTGCGGTGAGCTA | 55833 |
rs532360751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959793 | GTTAATTTCAACTGT[A/G]ATCCAAAATACAGAC | 55833 |
rs532409010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006051 | GCCTGGCCACCACAG[C/T]GAAACCCCATCTCTA | 55833 |
rs532424771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957650 | ATACATATTCTTTTT[A/G]TGTTTTCAATGTGGG | 55833 |
rs532444575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040062 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 55833 |
rs532446379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945584 | ACTCTCCCATACTTG[C/G]TCCACAAAGGCAAAC | 55833 |
rs532457387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039387 | AACGGGCCATGATGA[C/T]GATGGCGGTTTTGTC | 55833 |
rs532466067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951902 | AAAAGACTCTGGTGC[A/G]TCAATTAAAAATCAG | 55833 |
rs532467906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943246 | ATTGGTTGCTAAGGG[A/G]CAGGGCAATGAAGAA | 55833 |
rs532471315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953571 | GTGAATTTACATTAA[A/T]AATCAAATGAGGAGA | 55833 |
rs532497309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038474 | TTTTTTGGTGGAGAC[A/G]GGGTTTCGCTGTGTT | 55833 |
rs532564443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936493 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 55833 |
rs532591408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986302 | TAAGTTCTAATGTTC[A/C]ACAGTAGAGTAAGAT | 55833 |
rs532610947 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033580 | AACTTAATTGTATAC[-/T]TTTTTTTTTTCTCCT | 55833 |
rs532648225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038102 | CACGGGGAGTTCAAG[G/T]CTGCAATGAGCTAGG | 55833 |
rs532665085 | in-del | -/ATA | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954665 | GAGTTCCTCTCCCTT[-/ATA]ATAGACTATAGCCAA | 55833 |
rs532671468 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958106 | AGCTGGGACTACAGG[A/C]ACCTGCCATCACACA | 55833 |
rs532672247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992294 | TCGGGAGGCTGAGGC[A/G]GAAGAATCGCTTGAA | 55833 |
rs532684621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000529 | TCATCTCTGTACAAC[A/G]GTCTATTAAATCTAA | 55833 |
rs532703523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980294 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGGTCACT | 55833 |
rs532713214 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980158 | CATTCTAATAATTCC[A/G]CTTTAATCCAAATCC | 55833 |
rs532734385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004641 | TACAAAAAATTAGCC[A/G]AGCGTGGTGGCGGGC | 55833 |
rs532735063 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040980 | CAAACCAAAAATTCC[A/T]CTCTCAGTTATGTAG | 55833 |
rs532743905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014183 | TGCAAAAAAGTTAGC[C/T]GGGCATGGTGGCTCA | 55833 |
rs532757787 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019002 | TGTGACATATATACA[A/C]AATGGAAAATTATTC | 55833 |
rs532759926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048139 | GGCAAACAACTGAGT[C/T]GTAATGCACCAATGA | 55833 |
rs532785294 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992845 | CAACCTCTGTTATCG[C/G]TATTTTGCTAGTTGC | 55833 |
rs532801419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027557 | ACCCCATTTCTATTA[C/T]TTAAAAAAGAAAAAA | 55833 |
rs532811118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020594 | GCCTCCCAAAGTGCT[A/G]AGATTACAGGCGTGT | 55833 |
rs532811479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980738 | AGGTGGGCGGGTTGT[C/T]TGAGCTCAAGAGTTT | 55833 |
rs532852640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940213 | TCTTTGGCTCTAGAA[A/C]GGCTTCTTCCTAAAC | 55833 |
rs532858770 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035987 | ATTCCTGAGTGACAG[A/G]GTAAGACCCTGTCTC | 55833 |
rs532863848 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033120 | CTCACTGCTGGGTAT[A/T]TACCCAAAATAAGGG | 55833 |
rs532871188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035309 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGTG | 55833 |
rs532871231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041525 | AACATGGTGAAACCC[C/T]GTCTCTACTAAGAAT | 55833 |
rs532910193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996476 | TTTACAATGAGGACA[C/T]GTTTACTTATTTTTT | 55833 |
rs532950337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003597 | TTTTTAGTACAGATG[C/T]GGTTTCACCATGTTA | 55833 |
rs532958485 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991501 | GAGGTCCTTGATAGA[A/C]AAAGCAAGCTATCAG | 55833 |
rs532961349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940921 | AACCAAAAAATTAGC[A/G]CAACTTTCTTTATTG | 55833 |
rs532967692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955392 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 55833 |
rs533044513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978184 | GCATTTTATTAAATG[C/T]TATGTGGAACAAGGA | 55833 |
rs533082785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983942 | TTTGAGACAGAGCAT[C/T]ACTCTGTCACACAGG | 55833 |
rs533086176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948195 | AGAACAACAACAAAA[A/G]CAAATAAATGCAAGT | 55833 |
rs533095276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030263 | ACCCTGGCTAACACG[A/G]TGATACCCCATCTCT | 55833 |
rs533140779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983470 | AAGAAGCTGGGTTAC[C/T]ATGTATTCCTAAAAC | 55833 |
rs533140908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931503 | CAGAGGACAGCTCCA[C/T]GGCACTCCTGCTGAG | 55833 |
rs533165086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981687 | ACATTGATATAGAAC[C/T]GCTTGAGTTCATGAG | 55833 |
rs533187049 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030031 | ATAGGCCAGGCACGG[A/T]GGCTCACGCCTGTAA | 55833 |
rs533192118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989497 | TGAGCCACCGCGCCC[A/G]GCACATGCACGTATC | 55833 |
rs533202812 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987539 | CCTGAGCCCAGGGAG[A/G]TCAAGGCTGCAGTGA | 55833 |
rs533231367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989371 | CACGCCCAACTAATT[C/T]TTTGTATTTTTAGTG | 55833 |
rs533263176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977455 | TAGTAACATTGGTTT[C/T]TGTGTATATACCATT | 55833 |
rs533277606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024180 | CCCGACCATCTCTAC[C/T]AAAAATACAAAATTA | 55833 |
rs533277952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940736 | GTGTGCTGTGATCGC[A/G]CCACTGGACTCTAAC | 55833 |
rs533330195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938984 | AAGGGAGGATGATCC[A/G]TCCAAGACGGACAAG | 55833 |
rs533346684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976685 | GAAATGTATGGTATG[C/T]AAATTTTGTAAAGAA | 55833 |
rs533348679 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008950 | AGCCTGGCGACACAG[C/G]GAGACTGTCTCAAAA | 55833 |
rs533367058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938194 | AGGCAGGGTCTCATC[A/G]TGTTGTCCAGTCTGG | 55833 |
rs533375041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946554 | TTCTCTATGGGGCCA[C/G]ATAGTACAACAACCT | 55833 |
rs533384030 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037838 | AATATGTAAATACAG[-/A]AAACCCCGACTGGAT | 55833 |
rs533395176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034346 | TTTAGTAAAAGTATA[C/T]TGCTTTTATTTTACT | 55833 |
rs533397118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023535 | CATTAAGACTATATC[C/T]CCTTCCAATCATCAA | 55833 |
rs533431451 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975995 | CCAAGGCAGGAGGAT[A/C]GCTTGAGGCCAGGAG | 55833 |
rs533454255 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943058 | CCACCAACTAATGAA[C/T]GAATAAAATGTGGTA | 55833 |
rs533486432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028613 | TCAAACTCCTGACCT[G/T]AAGTGATCCGCCTAC | 55833 |
rs533543324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968723 | TCTATCCTTTTACAA[C/T]AGACAGTTGAATAAT | 55833 |
rs533563669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953909 | ATTCAATAAGTTTCA[C/T]TTTTTTTTTTTTTCT | 55833 |
rs533579020 | snp | A/T | | | intron-variant, nc-transcript-variant | UBAP2, SNORD121A | GRCh38.p7 | 9:33952834 | CTTGGAAATTACCAC[A/T]TCATTGTTTTCTGGA | 55833 |
rs533643899 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949728 | GTGCGCGCATGCACG[C/T]GCACACACGCACAAG | 55833 |
rs533650908 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034569 | ATACCCCACATCCTT[A/T]TATGTCTAAAGAACC | 55833 |
rs533678624 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004840 | GGGCACGGTGACTCA[C/T]GCCTATAATCCCAGC | 55833 |
rs533693479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041822 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCTA | 55833 |
rs533716198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969601 | GTGGGGCACGGTGGC[C/T]TACGCCTATAATCCC | 55833 |
rs533718263 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028468 | CACTGCAACCTCTGC[C/T]TCTTGGGTTCAAGCG | 55833 |
rs533733459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975573 | GGAGGCCGAGACGGA[C/T]GGATCACAAGGTCAG | 55833 |
rs533752712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939300 | CTCCCAGGTTCAAGC[A/G]ATTCTCCCACTTCAG | 55833 |
rs533754287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039620 | ATAAAGGGCGGTGCA[A/C]GATGTGCTTTGTTAA | 55833 |
rs533771727 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981833 | GGAAGCGGGGAAGGA[G/T]GGAAGGGGGGAAAGG | 55833 |
rs533801237 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982592 | CGGTATATATACTGA[A/T]GAGAAAATTATATGA | 55833 |
rs533802233 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987624 | AAAAAAAGTGAAAAA[A/T]ATATATATATATGAA | 55833 |
rs533842693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976221 | AAATTAAACAAGCTA[C/T]AAAACAAGGAAACTA | 55833 |
rs533879222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938506 | TTGAAACAAAAACAG[A/C]TTGTCATTGGCCGGG | 55833 |
rs533887222 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964269 | AGCCAATACCATTCT[C/G]TGAGGCCTCTGGAAA | 55833 |
rs533900002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930108 | GATGTACAACCTCAT[G/T]AAAAACTAGACTGAT | 55833 |
rs533907027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987719 | TCTTTGTGGACTTGC[C/T]GTGAAGTTTTTGCTT | 55833 |
rs533914712 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029062 | TCAAGGCTGCAGTGT[A/G]CTATGATCATGTCAC | 55833 |
rs533995525 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014096 | GGGAGATCAAGGGGG[A/G]GACAGATCACTTGAG | 55833 |
rs534011073 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022431 | GCAACACAGCAAGAC[C/T]CCTTTTTTTTTTTTT | 55833 |
rs534014149 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028806 | CTCTCCTACAAAAAG[A/G]AAAAAAAAAAGCAAA | 55833 |
rs534023673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930818 | GGAGGATCGCTTGAA[C/T]CCGGGAAGTGGAGGT | 55833 |
rs534061617 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941423 | ATACTACACGCATGC[C/T]TGGTTTTCTCCACAA | 55833 |
rs534095090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945236 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 55833 |
rs534100908 | in-del | -/A | 0.00862924 | 0.0651165 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971633 | AAACTCATCTCTGGC[-/A]AAAAACAGAACACTT | 55833 |
rs534126382 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939890 | GGGAGGAGGAGGAGG[A/G]GGGGAGGAGGAGGAG | 55833 |
rs534180309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980507 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55833 |
rs534183456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959992 | ACCCAGGCTAGAGGG[C/T]GGTCGAATGATAATG | 55833 |
rs534188670 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974623 | TCTGGAACACACAAA[A/G]AACTCCTAAAACTCG | 55833 |
rs534206676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046115 | ATTTGCTGACATACA[A/G]GTTTCTCACAAGGAA | 55833 |
rs534212199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039164 | GGCAGCCTCCGCCCA[A/G]CCAGCCGCCCCTTCC | 55833 |
rs534268765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045520 | CTGGGACTACAGGCA[C/T]GCGCCACCACACCAG | 55833 |
rs534288137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927694 | ACGCAGCGCACTCGG[C/T]GGGCCTGAGACTCTC | 55833 |
rs534292474 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930328 | CCGCTACATACAGCT[A/G]TACACATGAAACAAC | 55833 |
rs534294123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974176 | GCCTGGGTGACATAG[C/G]AAGACTCTGTCTCAA | 55833 |
rs534298233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980793 | AAACCCTCTCTCTAC[A/G]AAAATTAGCTGGGCA | 55833 |
rs534324516 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002101 | AGCAACCATGGCAGC[C/T]ACCATGCCTGGCTAA | 55833 |
rs534326709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933685 | TTCTAAAACCAATCC[C/T]AAGTGCCTGAAAATA | 55833 |
rs534353722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983654 | TTTTTGTTACCTTCT[A/G]TTTTCTTTTTCTTCC | 55833 |
rs534371717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007875 | CTCTATCTCCTGACC[C/T]CATGATCTGCCCGCC | 55833 |
rs534372696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018642 | GCCAAGGCGGGAGGA[C/T]CACAAGGTCAGGAGA | 55833 |
rs534395424 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921703 | CCATGCATGCTCTCA[A/G]AACTTTATTAGGTGG | 55833 |
rs534439527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007209 | GTTCTAGTACTCAAG[C/T]GAGGCCAGGTGCAGT | 55833 |
rs534446265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014716 | AAGAGAATCACTTGA[A/G]CCCGGGAAGTGGAGG | 55833 |
rs534463873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001759 | TATTTTCTGCTCCCT[A/G]TGTTTCAAACCTAAA | 55833 |
rs534465317 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049097 | AAGGAACAAATAAGG[C/G]AGACTTGATAATATG | 55833 |
rs534466686 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955528 | CCGTCTCAAAAAAAC[-/A]AAACAAAACAAAAAA | 55833 |
rs534503935 | snp | A/G | 0.000115421 | 0.00759587 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963767 | GACAGATCCTGAGCT[A/G]TGTTGTGAGTATTTG | 55833 |
rs534537096 | in-del | -/AAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979728 | TCTACTAAAAAATAC[-/AAG]AAGTAGCTGAGCCTG | 55833 |
rs534539505 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977644 | GGGACTCTACTACAT[C/T]TCTGTTGAATGATTG | 55833 |
rs534549028 | snp | C/T | 6.35062e-05 | 0.00563463 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922450 | AAATACGTGCTCGTG[C/T]GTTCTCTCCTGCCCA | 55833 |
rs534555786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959149 | GAGAGCAAGGCCCTG[C/T]CTCAAAAAAAAAAAA | 55833 |
rs534559498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011603 | AACAAAGCACCAAAC[A/G]TAAGAGTATAATAGG | 55833 |
rs534587959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043418 | GTGATTCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 55833 |
rs534602352 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959422 | AGTGTGCGTCATTGT[A/G]TATAGTTTTGAGGAT | 55833 |
rs534640584 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005949 | TAAGAACTGGACTCT[A/G]GCCAGGCGTGGTGGC | 55833 |
rs534642786 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049668 | TGCCCTCCCAAGCCC[C/T]TTCTGGGTGAAAAGA | 55833 |
rs534645000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042771 | TGGTTGTTCATTTTA[C/T]TTTTTTTTTTTAATT | 55833 |
rs534676756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971525 | GAATAGTTTCAGAGG[C/T]AGGACAGTAGCCTGT | 55833 |
rs534686480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962696 | TAATTAAAAAATAGG[A/G]CCTGGAGCAGTGGCT | 55833 |
rs534692949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009955 | TGGGATTACAGGCAT[A/G]TGCCACCATGCTTGG | 55833 |
rs534696469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969974 | CCACTCTGTCACCCA[A/G]GCTAAAGTGCAGTGG | 55833 |
rs534734763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017801 | GCATGGTGGCAGGCA[A/T]CTGTAGTCCCAGCTA | 55833 |
rs534764898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003687 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACAC | 55833 |
rs534774892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933108 | CGTTTCTTCAGCCAT[A/G]GAAAGTTCAAGTCAG | 55833 |
rs534825835 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928795 | AAGCTCTGTAAGAGG[C/G]AGACCAGTCTCCAAA | 55833 |
rs534854931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961616 | ATGCCCATAGATAAT[G/T]GTTTTAAAGGAAATA | 55833 |
rs534880221 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037209 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 55833 |
rs534880441 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957322 | TCTGGCATACATAGG[A/C]CCCCATGAAACCATC | 55833 |
rs534882078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997504 | ACTATACCATTTGGC[C/T]TCCCTGCTTTCATCT | 55833 |
rs534894497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996767 | GGACAATATTCCATA[C/T]GCTGGCTTTCACCAT | 55833 |
rs534899546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036881 | GTGGTGCGATCTCAG[A/G]TACCTCACTGACCTC | 55833 |
rs534908314 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034340 | TCTTTTTTTAGTAAA[A/G]GTATATTGCTTTTAT | 55833 |
rs534956626 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961936 | ACCTGATTTCAGATT[A/G]GGGTGGCTCTCTGTG | 55833 |
rs535005335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030172 | CCAGGTGAGCCGGGC[A/G]CGGTGGCTCACGCCT | 55833 |
rs535100718 | snp | A/G | 9.9481e-05 | 0.00705199 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932572 | CTTACTGTGTGTGAC[A/G]TGCTCGAGGAGAGGG | 55833 |
rs535100790 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966470 | GAAAAAAAATAAAAT[-/A]AAAAAAAAGAATCAA | 55833 |
rs535102212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041108 | AATATCCATCAACAA[C/T]GAAATAGACAACATA | 55833 |
rs535109755 | in-del | -/CTCA | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022904 | TTATCTGATCTTTTT[-/CTCA]CTGTTTATTCTCAGT | 55833 |
rs535166039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047663 | ATAAAAGATAATCTT[C/T]GGATACCTTATGGAG | 55833 |
rs535170533 | in-del | -/TTTAT | 0.00914312 | 0.0669923 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016554 | ACTTTTTATTTTTTA[-/TTTAT]TTTATTTTTTTTTTT | 55833 |
rs535189173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035595 | GAGGCTGAGGCACAA[C/G]AATCACTTGAACCTG | 55833 |
rs535232456 | in-del | -/GAAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029694 | AAATAAAAAGAAGAA[-/GAAG]GAAGAAATGCGGCCA | 55833 |
rs535244482 | snp | A/G | 9.88598e-05 | 0.00702995 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923487 | GAGGGACCTGGGGGG[A/G]CAAGCAGATGAGGTA | 55833 |
rs535253763 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948387 | ACCAAGATGACTGAG[A/G]ACTGAGGACTGGGAT | 55833 |
rs535263899 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921620 | CTATGACCATGTGGG[A/G]TCTCCTTTAGCCCTG | 55833 |
rs535277582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970834 | TTGAGATGAAGTCTC[A/G]CTCTGTTGCCCAGGC | 55833 |
rs535334129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017754 | ACACAATGAAACCCC[A/G]TCTCTACTAAAAATA | 55833 |
rs535344425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983166 | TACAGATGTGAGCCA[C/T]GGTGCCCGGCCCCCC | 55833 |
rs535356434 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032471 | CAGGAAAGGGGATAA[A/G]GGAGGAAAACCACCT | 55833 |
rs535405552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962595 | AGGTTGCAGTGAGCT[C/G]AGATCATGCCACTGC | 55833 |
rs535433203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016240 | GAGGAAGAGGAAGGG[A/G]AGGAAGAGGAGGAGG | 55833 |
rs535433627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008560 | ACCAGCCTGGCCAAC[A/G]TGAGACCCCGTCTCA | 55833 |
rs535440260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983099 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 55833 |
rs535455499 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031599 | GGCATGAGCCACCAC[A/G]CCCGGCCTTAACTTG | 55833 |
rs535466549 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006094 | AAAAATTAGCCGGGC[A/G]TGGTGGCGTGCACCT | 55833 |
rs535480717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989191 | TTATCAAAGGCACAT[A/G]CATGTATCTTTCTTT | 55833 |
rs535480764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982693 | TTATCTAGCATACTT[A/G]CGATTAAGAAAAACT | 55833 |
rs535488604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017279 | ACTTACAATAAAAGA[C/T]AAAAGCTCTCTGGAA | 55833 |
rs535496095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015423 | TCCCGGGTTCAAGCA[A/G]TTCTCCCTGCCTCAG | 55833 |
rs535499464 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030269 | GCTAACACGGTGATA[C/T]CCCATCTCTACTAAA | 55833 |
rs535515405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977536 | AAGATCCAGAGTCTT[G/T]TAATCACAAAAACCA | 55833 |
rs535544163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002446 | TGCATGGCGCGATAT[C/T]GGCTCACTGCAACCT | 55833 |
rs535547436 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977185 | CTGGGATTACAGGTG[C/G]CTGCCACCACGCCTG | 55833 |
rs535551274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023914 | CCGGGCATGGTGGCA[C/T]GCACCTGTAGTCCCA | 55833 |
rs535613280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046383 | TGCCGGGCGGGGTGG[C/T]TCACGCCTGCAATCC | 55833 |
rs535625575 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010773 | CAAACATTTTTTTTT[A/T]AAAAGTAAAATTATG | 55833 |
rs535691415 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010253 | ACATGGTGAAACCCC[A/G]TCTCAACTAAAAATA | 55833 |
rs535694630 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039332 | GCCCCTCTGCCCGGC[C/T]GCCACCTCATCTGGG | 55833 |
rs535722627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958815 | GCACAGGAGTTTGGG[A/G]CTGGAGTGAGCTGGC | 55833 |
rs535725231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984241 | ATGGTCTCCAATTTA[A/G]CCTCAGCATTAAGGA | 55833 |
rs535726801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041979 | GCAGTGAGCCAGGAT[C/T]GAGCCACTGCACTCC | 55833 |
rs535737454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028954 | CTCGTCTATACAATA[A/G]ATTTTTTTTTAATTA | 55833 |
rs535737509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035359 | GTACAAAAATTAGCC[A/G]GGCATGATGGCGGGT | 55833 |
rs535746693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034756 | CATGAGCCTATAGTC[C/T]CAGCTACTGGAGAGG | 55833 |
rs535799593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996510 | GGCCATTCCATGCAT[A/G]TCTTTTCACTAACAC | 55833 |
rs535825496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005691 | AGAGATAAATAGGAA[C/T]GGGAGAAAAGAAAGC | 55833 |
rs535833350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968522 | AAAGTCTCCATGTTG[A/G]TGGAATCAAGGGCCA | 55833 |
rs535853845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964529 | AGCACAGCTTCCACA[C/T]ACAGTTCTTCCACAC | 55833 |
rs535860800 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950261 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55833 |
rs535869019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975525 | AAAATGGGGCCAGGT[A/G]CAGCGGCTCATGCCT | 55833 |
rs535910453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006183 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 55833 |
rs535910740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999293 | TGGGCAACATAGAGA[G/T]ACCCTGTCTCTATTT | 55833 |
rs535918760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960699 | GCAGAAGAACTGCTT[A/G]AATCTGGGAGGCAGA | 55833 |
rs535920814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954145 | CTCCTGCTCTCAAGT[A/G]AGCTGCCTGCTTTGG | 55833 |
rs535922548 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970314 | AGTGTTTTCAAATAA[C/T]AACTTATAAATTTTG | 55833 |
rs535934710 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923052 | GGAGGAAAAGCAGTT[A/G]TTCCCCACAGCAGTT | 55833 |
rs535947346 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964042 | TACCAAGCTCCCTTC[A/T]CACTCATCAAAGAGA | 55833 |
rs535950886 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935558 | GGGCATCAGCCACCC[C/T]GCCTGGCCCAAGCAT | 55833 |
rs535962214 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988737 | TATGAAACTACTCAG[G/T]TGCCACTCATTTCTA | 55833 |
rs535970128 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947669 | ACATTAAAAAAATAC[-/A]AAAAAATCAGCCAGG | 55833 |
rs536004909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996002 | TAAGGCTGGAGTAGA[C/T]CACCAAGTTCTCTTT | 55833 |
rs536017583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992556 | CAGCGCAAGACTCCC[A/G]TCTCAAAAAAATAAA | 55833 |
rs536034553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038243 | ATCATGAGGTCAGGA[C/G]TTCAAGACCAGCCTG | 55833 |
rs536039273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954710 | CAATGATCCCAGTAA[A/C]TTCACTGAATCATAA | 55833 |
rs536048738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002885 | TACAAACAAGGTTCC[A/G]CCATGTTGCCCAGAT | 55833 |
rs536139894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032441 | TCCCACTAGTTACTC[C/T]GTCCCAAGGCTTCAC | 55833 |
rs536149114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936171 | TATTTTCTGTAGAGA[G/T]GGGGTTTTGCCATGT | 55833 |
rs536150583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031939 | CCCAGGAGTTTGAGA[C/T]CAGCCTGGGTAACAT | 55833 |
rs536177710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985807 | CAGGTGGATCACTTG[A/G]GGCCAGGAGTTTGAG | 55833 |
rs536186399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943404 | TTGCTTCATAACAAA[A/G]GACTAAATTCAGTAC | 55833 |
rs536187943 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947453 | ACAATACAAACCACG[A/G]AATGTAAAGGTTGAT | 55833 |
rs536215391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042604 | CCACCCTGGGCAACA[C/T]AGCTAGACCTTGTCT | 55833 |
rs536224574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013287 | TGCTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55833 |
rs536242913 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045806 | ATTCTTTGAGTTAGT[-/A]AAAAAAAGGATCCTA | 55833 |
rs536311518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957709 | TGATCTAATGAGGTA[A/C]CACGGAAAACATAAA | 55833 |
rs536348068 | in-del | -/A | 0.159767 | 0.233148 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945142 | CTTCATCCAAAAATT[-/A]AAAAAAAAAAAACTT | 55833 |
rs536369595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990929 | GGCATAAGCCACTGC[A/G]CCTGGCCTATTTGGT | 55833 |
rs536390592 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050595 | CTGCCGGGCGTGGTG[A/G]CTCACACCTGTAATC | 55833 |
rs536391065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949875 | GTTGTTTAGATGACT[A/G]AGAACACCAAATACG | 55833 |
rs536392091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965457 | TTTTGATAAAATGTA[C/T]TTTGTCAATTTTCTC | 55833 |
rs536393221 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003219 | TGGTTTTGGTAGAGA[C/T]GGGGTTTCACCATGT | 55833 |
rs536394678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043669 | CAGTTAATTTTTACA[A/T]TTTTTTTATAGAGAC | 55833 |
rs536396115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957434 | TGTCTGCATCCCCAG[A/G]CAACCACTCACATGC | 55833 |
rs536441655 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977021 | GGTCTTGGAAAAAAC[-/A]AAAACAGTTGTTTTT | 55833 |
rs536446067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984910 | AACCCAGGAGTTCAA[C/G]ACTGCAATGAGTTAT | 55833 |
rs536499555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019311 | AGGAAGCTGAAGCAG[A/G]AGAATTGCTTGAACC | 55833 |
rs536519679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972746 | AAAAAGGTATCACTC[A/G]TACATAAATAAGCAT | 55833 |
rs536559002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038608 | TGCCCAGGCTGGAGT[C/G]CAGTGGCGTGATCTC | 55833 |
rs536616785 | snp | C/G | 3.46176e-05 | 0.00416024 | missense | UBAP2 | GRCh38.p7 | 9:33922555 | TTTGGAGGCTTGAGA[C/G]TTGGGCTGCAGGGAG | 55833 |
rs536621622 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036324 | GTTTCTCCATGTTGG[C/T]CAGGATGGTCTCAAA | 55833 |
rs536649680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004842 | GCACGGTGACTCACG[C/T]CTATAATCCCAGCAC | 55833 |
rs536654022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997695 | TCCCCAGTGATCAGA[C/T]TATTGACAGACAGAA | 55833 |
rs536660102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928247 | TAAGCTTTAATGACC[A/G]CAACTCTCTGTAAAA | 55833 |
rs536669460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949270 | AACTAAAGAGGAATG[C/T]CATGAAATACATGAC | 55833 |
rs536670678 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966484 | ATAAAAAAAAGAATC[A/C]AGTTGTCAAAAATCT | 55833 |
rs536674489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978532 | AATCCTAGCACTTTA[C/T]GAGGCCAAGGCAGGC | 55833 |
rs536750136 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926177 | CACTCAGCTGATTGC[A/G]GAAGAGCAGTCACTG | 55833 |
rs536783596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941345 | AGAGAGAAAGCAGTA[A/C]ATGAAATATTCAGAG | 55833 |
rs536811696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977134 | ACCTCCACCTCCCAG[A/G]TTCAGGCAATTCTCC | 55833 |
rs536866755 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003291 | CCACCTTGGCCACCC[A/G]AAGTGCTGGGATTAC | 55833 |
rs536870307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942447 | AACAACAACAAAGTC[A/G]GCCAGGCCGGTGGCT | 55833 |
rs536875748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030804 | GCATAGTGGCAGGCG[C/T]CTGTAGTCCCAACAA | 55833 |
rs536898676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942694 | AAGCATGCTGCTGCA[C/G]TCCAGCCTGGACAAC | 55833 |
rs536936340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930315 | ATCACGTACTGACCC[A/G]CTACATACAGCTATA | 55833 |
rs536938863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038176 | AAAAAAAAGGTCGGG[C/T]GCGGTGGCTCCTGCC | 55833 |
rs536940329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928895 | GACCCAACCTGCCTG[C/T]GCAGACTAACTCTCC | 55833 |
rs536940873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031059 | AGACTAGCCTGGCAA[A/G]GTGGGAGTCAGGAGT | 55833 |
rs536951317 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037668 | AGTTATTTCTTGCTT[A/C]TCAGATGACCTGACT | 55833 |
rs536958132 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954794 | ATATACTATAAGACA[C/T]AATCATTAATCATTT | 55833 |
rs536964381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971874 | CAGCCACTGTAAAAG[A/G]CATCACCTCTCCTTC | 55833 |
rs536968409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018732 | GCCAGGCGTAGTGGC[A/G]GGCGACTGTAGTCCC | 55833 |
rs536985840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950889 | TTTAAAATGTATACA[A/G]TACACACATGTGCAT | 55833 |
rs537011811 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956430 | TTCAAGCGATCATCT[C/T]GCCTCAGCCTCCTGA | 55833 |
rs537021569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048414 | AGTCCCAAGACTAGC[C/T]ACGGGCGTGAAAGCG | 55833 |
rs537023735 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931304 | CTGCATATATGGAGG[A/G]ACAACTGTATTAGCA | 55833 |
rs537034848 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049857 | AATTAATGACCTCCT[C/T]TCAATAGGATCTGAC | 55833 |
rs537037890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004492 | GGTCACAAAAAAAGG[A/G]AAAAAAAAGGCTGGG | 55833 |
rs537044974 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047764 | GTGAAAGAATCGCTT[A/G]AACCCAGGAGCTGGA | 55833 |
rs537106039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964492 | CACTTGCACAACATT[C/T]GGCTTCAAAGCCATG | 55833 |
rs537123181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997634 | TCTGTACTAAGTGAA[C/T]GCCTGCAACATACAA | 55833 |
rs537137970 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927680 | AAGGTCAGTGGAACA[C/T]GCAGCGCACTCGGCG | 55833 |
rs537148991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963940 | CCATACTCTTACAGG[G/T]CACTGCAAATCAAGT | 55833 |
rs537197385 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049164 | CGCATACAAGGTGCC[C/T]ACAACTGCAGCTCGT | 55833 |
rs537263363 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037642 | AATTACCTGAACTAA[C/G]TAACAGCAGTAGTTA | 55833 |
rs537286509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989933 | GTTTTGGTGGGTTTT[A/T]AAAAAATTTATAAAG | 55833 |
rs537300128 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024903 | GCAGGAGAATCACTT[C/G]AACCCGAGAGGCGGA | 55833 |
rs537300731 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034527 | ATACAAAATTCCTTA[A/T]TAAAGAAAACACTAC | 55833 |
rs537317605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991605 | CATTATTTAAGTGAG[C/G]ATGTTTAATTTGATT | 55833 |
rs537326736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000030 | TTGGCTCACTGCAAC[C/T]TCTGCCGCCCAGGTT | 55833 |
rs537342064 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931181 | CATAATTTGAAAACA[A/C]CCATATTTGGAAGGC | 55833 |
rs537354212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957526 | CAAACCTTTATTCCT[A/G]GCTTCTTTCACTCAG | 55833 |
rs537362685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984242 | TGGTCTCCAATTTAG[C/T]CTCAGCATTAAGGAA | 55833 |
rs537408977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041185 | GGGCCGGGCACGATG[A/G]CTAACACCTGTAATC | 55833 |
rs537414112 | snp | A/C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968200 | GATATTTGGTGCATT[A/C/G]GATTGGTACAGGATT | 55833 |
rs537428382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959098 | GGCTGCAGTGAGCCA[A/T]GATCGTGCCTCTGCA | 55833 |
rs537430975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955545 | AACAAAACAAAAAAA[A/G]GGGCCAGGTGTGGTG | 55833 |
rs537535647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036267 | GGTTACAGGCACCCA[C/T]CGCCATGCCCGGATA | 55833 |
rs537581377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962440 | ATCACGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 55833 |
rs537596718 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990540 | TATACTATCACCTGA[C/T]AGTTAAGGTGAAACA | 55833 |
rs537600510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987603 | GAAAGAGTGAGACCT[A/T]GTCTCAAAAAAAGTG | 55833 |
rs537648090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981044 | TCAAGACCAAAAAAA[C/T]AATATGGGCTTATTT | 55833 |
rs537665841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941135 | GAAAGCAATACAACT[A/G]GCAATGACCATCAGA | 55833 |
rs537668377 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024216 | GCGTGGGGGCACATG[A/C]CCATAATCCCAGCTA | 55833 |
rs537685083 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987147 | CAGGCACAGTGGCTC[A/T]CACCTATAATTCCAG | 55833 |
rs537763477 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981776 | AGGTAGGTAGGTAGG[A/T]AGGTAGGAAGGAAGG | 55833 |
rs537766062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024366 | AAAAAATAGCAAATA[C/T]ATTCTTTGAAAAATA | 55833 |
rs537766757 | snp | C/T | 4.9423e-05 | 0.00497082 | missense | UBAP2 | GRCh38.p7 | 9:33941719 | CTGTTATGCACAGAA[C/T]TCTGGTCATAAGAGG | 55833 |
rs537769192 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021792 | ACGCCTGCCACCACG[A/C]CCGACTAATTTTTGT | 55833 |
rs537807275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038699 | TAGCCTCTGCCCGGC[C/T]GCCACCCCGTCTGGG | 55833 |
rs537841286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007775 | TCCCGAGTAGCTGGG[A/C]CTACAGGCACCCGCC | 55833 |
rs537900803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945034 | CTTTGGGAGGCTGAG[G/T]TGGGAGGATTGCTTT | 55833 |
rs537941424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039090 | TCCGCCCGGCAGCCA[C/T]CCCGTCTGGGAAGTG | 55833 |
rs537945066 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013011 | CTACTAAAATTAGCC[A/G]GGTGTGGTGATGTAC | 55833 |
rs537960468 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033971 | GAACTCCTGACCTCA[G/T]GTGATCCACCTGCCT | 55833 |
rs537969058 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979848 | ACTCCAGCCTGGAGA[A/C]AGAGTGAGACTCTGT | 55833 |
rs537970461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993844 | CCACACTATAAAATC[A/G]TTCAAGAGGTAACCA | 55833 |
rs537971129 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026427 | CATAATGGGCTAAGG[A/G]TTCAACTACTAAAAA | 55833 |
rs537983554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936105 | CCTCCCCCTTAGCCT[G/T]CCTAGGAGCTGGGAC | 55833 |
rs537986961 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952930 | CCTGGAGTACAGAGG[A/C/T]ATGATCATGGCTCAC | 55833 |
rs538059507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937662 | CCTGTAATCCTGGCA[C/T]GTTGGGCAGCTGTGG | 55833 |
rs538061928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930067 | CATAAAGGAAATCAA[A/G]TGGTTTTCAAATATA | 55833 |
rs538068429 | snp | C/G/T | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33923841 | GGCATGCCTGTGTAG[C/G/T]AGGGAAGACCAGTGT | 55833 |
rs538074955 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935410 | CTGGGATTACAGGCA[C/T]GCGCCGCCACCACAC | 55833 |
rs538117755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958501 | CTGCAAGTGCCTCCC[A/G]GGTTCAAGTGATTCT | 55833 |
rs538133571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045056 | CATTGTTTACAAACG[A/G]GTAAAAAAAGGCTGG | 55833 |
rs538135252 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931608 | CTTTGAAAGTGGCAG[G/T]TTGTGTGTTTTATGA | 55833 |
rs538141623 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974173 | CAAGCCTGGGTGACA[C/T]AGCAAGACTCTGTCT | 55833 |
rs538161025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028240 | TAGGACATCAAAATT[G/T]ATTTGATATCGTCAC | 55833 |
rs538176325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931016 | GGTAGAGCCAAGTAG[A/G]TGAGAGACAGAAAAA | 55833 |
rs538176640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938413 | TGGGGTTCCAGACAT[A/G]AGCCACCATGCCCAG | 55833 |
rs538193291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985685 | GGTATAGAGGGTGGG[A/G]AATAAAGAGAGATTG | 55833 |
rs538220198 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947341 | CTATTCCTTAATACA[G/T]TGTGGCATGTGAGTG | 55833 |
rs538230868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000269 | ACAGGTGCGCACCAC[C/T]ACATCTGGCTATTTG | 55833 |
rs538232506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966475 | AAAAATAAAATAAAA[A/T]AAAGAATCAAGTTGT | 55833 |
rs538233605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957836 | GCAGGAGGTAGAGGA[A/G]ACAGTAGGTGTTCAT | 55833 |
rs538252317 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943317 | ATGATGGAAGGTCTG[G/T]ATAAACACTGAGGAT | 55833 |
rs538266657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990814 | GTGAATTTTTGTAAT[C/T]TTAGTAGAGACGGGG | 55833 |
rs538281258 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992346 | GTGAGCCGAGATCAC[A/G]CCATTACTCTCCAGC | 55833 |
rs538304548 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006340 | GAGAATGAAATTAGA[A/G]TATCAACAAACTTGT | 55833 |
rs538358771 | in-del | -/TT | 0.482905 | 0.0908579 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003376 | TACATCAAAGATGGC[-/TT]TTTTTTTTTTTTTTG | 55833 |
rs538394034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968665 | TTGTTAAATGGATAA[C/T]ACTAATTTCTATATT | 55833 |
rs538402078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993757 | CTGAACAAGTGTATT[C/G]TTTCACAACTATATT | 55833 |
rs538409382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986540 | GTTTTAAATTATTCA[C/T]AGGGCTTTCTCAGCT | 55833 |
rs538423205 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974081 | CCTCTAACTTAGCTA[A/C]CTGACAGGCTGAAGC | 55833 |
rs538472137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020621 | GTGTGCCACTGAGCC[G/T]GCCCAGAGCCAACGA | 55833 |
rs538503417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007164 | TAGACCCCTTTATTT[C/T]CTTCTCTTGCCTATT | 55833 |
rs538506683 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948333 | TGCCAAAGCTTGAAA[C/T]GTCCTCAGTAGGGGC | 55833 |
rs538515297 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974099 | GACAGGCTGAAGCAG[A/G]AGGATCCATGAGCCC | 55833 |
rs538568923 | snp | A/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922424 | ATTCTAGGAAAGGGC[A/G]CTGGGCTCCCAAATA | 55833 |
rs538575052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980531 | CAGGCGTGAGCCACC[A/G]CACCCGGCGAGCGTC | 55833 |
rs538595839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044424 | AAAAAAATTAGCTGG[C/G]CGTGGTGATGCATGC | 55833 |
rs538628116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037524 | TTTCAAAACTTAGGG[C/T]TGGCATAGCAGTCAT | 55833 |
rs538670494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950644 | AGGTTGCTACCAATT[C/T]GCAAAAATCCAGCTC | 55833 |
rs538670819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942007 | ATTTAACTGAGAGAT[A/G]GGGGGACATCTTTAA | 55833 |
rs538673451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014003 | CATCAATAATTTTCC[C/T]AATGCATACTAGTGT | 55833 |
rs538688060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952312 | TTCTTGTATAAGCTA[C/T]GATCTAAGCTTATAC | 55833 |
rs538700173 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991891 | CGCCGAAAGGTACTC[-/T]TATCTTTATAAAGGG | 55833 |
rs538773539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958462 | GCTGCCCAGGCTGGA[A/G]TGCAATGGTGTGATC | 55833 |
rs538783028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942548 | GTCTGGGCAACATGA[C/T]GAAACCCTGTCTCTA | 55833 |
rs538850212 | in-del | -/AT | 0.132867 | 0.220861 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945180 | TTTGGACTAATTGAT[-/AT]ATATATATATATATG | 55833 |
rs538859419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928920 | CTCTCCGCCGCCATC[C/T]CATGCCCACAGGTCA | 55833 |
rs538861280 | in-del | -/T | 0.337386 | 0.23423 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980410 | TAATCTTTTTTTGTA[-/T]TTTTTTTTTTTTAGT | 55833 |
rs538861520 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944470 | GCTGGGAAGCTGCAA[A/G]AGCTTGTTCACAGTG | 55833 |
rs538890880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979099 | AATTAGCTGGGCATT[A/G]TGATGTGCACCTGCA | 55833 |
rs538910967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965764 | TTAAAATCAGGGAGT[A/G]TGGGCCGGGTGCGGT | 55833 |
rs538934150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033327 | AACGTGGATAGAACC[A/G]GAGATCATTATGTTA | 55833 |
rs538940340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987038 | TACACTTGTAATTCC[A/G]GCACTTGTAATTTCC | 55833 |
rs538950175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973309 | ACTTCCTTCTTCATC[C/T]TATACTCACTACCCA | 55833 |
rs538971929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945000 | CCAGGCACAGTCACT[C/T]ATGCCTATAATGCCA | 55833 |
rs538990297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991541 | TATAGAATTACATTT[C/T]TTAGTTCAAATAGGA | 55833 |
rs539036540 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043292 | TCCTCCAACCTCAGC[A/C/G]TCCTGAGTAGCTGGG | 55833 |
rs539060258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947198 | GCTTCAAACCCCGGA[A/G]TGGTCTCATGTACTT | 55833 |
rs539065051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991028 | ACTGGCTCACGCCTG[C/T]AATCCCAGCACATTG | 55833 |
rs539070817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938616 | AGCCTGGGCAACATG[A/G]TGAAACCCTGTCTCT | 55833 |
rs539072567 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007590 | ATTTTTTCACATACA[-/T]TTTTTCAGCGTTTAT | 55833 |
rs539129592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025859 | AACTAGGATTACAGG[C/G]CTGAGCTACCATGCC | 55833 |
rs539155147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029461 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAATGAGC | 55833 |
rs539185259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009542 | TGAGATTACAGGTGT[C/T]AGCCACCATGTCCCG | 55833 |
rs539188129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929300 | CTGACTTGCTGAAAG[A/G]GACTCAAGAGTCATC | 55833 |
rs539250698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985504 | AAAAGAATGAAATCA[C/T]GTCCTTTGGAGCAAC | 55833 |
rs539268761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026359 | TTTACGTTTCAGGAA[C/T]AGAAAAACTAATGTT | 55833 |
rs539273144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019353 | GGTTGCAGTGAGCCA[A/C]GGTAGTGCCACTGCA | 55833 |
rs539285390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983005 | TGCCCCGGCCTCCAA[C/G]TAGCTGGGACTACAG | 55833 |
rs539289296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023776 | ACAGGCCGGGTGCAG[C/T]AGCTCACGCCTGTAA | 55833 |
rs539311298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961778 | GAGGAGGAGCATGCT[G/T]GTGAGACAAAAGAAG | 55833 |
rs539323001 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951637 | CAGGTGTGAGCCACC[A/G]CGCCCAGCTCCCAGT | 55833 |
rs539369477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008398 | CCTTCTGGTTCCCTT[C/T]GAACCAGGATGGTGT | 55833 |
rs539385730 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950021 | ATTTTTACATATCAA[G/T]ATCATTCTGAAATAT | 55833 |
rs539479365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987859 | AAACCCTGAGTTCTT[A/C]GAAAAACTAAAGTGT | 55833 |
rs539479717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995870 | TGTTATAATAGAGAT[A/G]TAAGAAGTAATCAGA | 55833 |
rs539508186 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932508 | AGCTGCATGTGACTA[A/T]GCTCCAGGCTCCCCA | 55833 |
rs539509808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015328 | ATTCAAATGGGTCTT[G/T]GTTTTATTGAGACAG | 55833 |
rs539513399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959284 | AGACCCAAGGAACAA[C/T]GCCCTGCCTAAGGTC | 55833 |
rs539523619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925629 | GCTGGTTTGCACAGT[A/G]GGGAGAAGCCGCTCC | 55833 |
rs539528133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028897 | AATTAGGAACTGGGC[C/T]GCACAGCAGGAGGTG | 55833 |
rs539569525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014741 | TGGAGGTTGGAGTGA[A/G]CCGAGACTGGCCACT | 55833 |
rs539599403 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992709 | GAAGCAATCTTTACA[A/G]TACCATAGTAACTGC | 55833 |
rs539613170 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046315 | TAAAAAAAAAAAAAA[A/G]AGGACTGGGAAATCA | 55833 |
rs539622922 | snp | C/T | 0.000644825 | 0.0179443 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926704 | TTTAGGAACCACATA[C/T]CACACCCTGGGAAGC | 55833 |
rs539650093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976491 | AACACAAAAACCTAC[A/G]GAAACAGAAAGGCGA | 55833 |
rs539659471 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020382 | CTGGAGTGCAACGAA[G/T]AGTGCGATCTCGGCT | 55833 |
rs539680721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016659 | CTCCTGAGTTCAAGC[A/G]ATTCTCCTGCCTTAG | 55833 |
rs539696699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954584 | ACATTCTCACCATGC[C/T]AATAAGACAGGCAGA | 55833 |
rs539704128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047801 | CCTGGGCAACATATG[A/G]AGACCATATCTCTAA | 55833 |
rs539731726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961870 | TAAGTAAAATGATGA[A/T]TGTTTCCTAGAAAAA | 55833 |
rs539732734 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014907 | GTGAATAAATTCCTA[C/T]CAGAGTAAGTGTATT | 55833 |
rs539733280 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982884 | TGTTTTTTTTTGTTT[G/T]TTTTTTTTTGTTTTT | 55833 |
rs539735688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034122 | CATTTCAACATTTGG[A/C]ACTCAAATGTCACAA | 55833 |
rs539748883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039881 | AAAAAAATACAAGCC[G/T]CACACGGTGGCTCAC | 55833 |
rs539750537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046682 | AAAAAAGAAGGCTTC[A/G]CTTCAGACCACTCCA | 55833 |
rs539770452 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029845 | ATACAAAAATTAGGC[C/T]GCTGTGGTGGGGGCA | 55833 |
rs539785659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925276 | CAGCCTAGAACCCCC[A/G]GAAGAGGCAGAGCTG | 55833 |
rs539790938 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959965 | TGCTTTAAGATGGAT[A/T]CTTGCTCTGTCACCC | 55833 |
rs539803933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987222 | TCAAGACCAGCCTGG[C/T]TAACACACGGAAACC | 55833 |
rs539829686 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976617 | TGATTGTGGTGATGA[C/T]TGCACAACTTGGTGA | 55833 |
rs539834817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974942 | GACTAAAAAAAAAGG[A/G]GGGGGTGCGGGGGGG | 55833 |
rs539851706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980876 | GGCTTGAGCCTGGGA[C/G]GTGGAGAGTGCACTG | 55833 |
rs539864669 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940740 | GCTGTGATCGCGCCA[C/T]TGGACTCTAACCTGG | 55833 |
rs539905826 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968471 | GGCTTCTTCAGCTTC[A/C]GGTTGGGACATTTGA | 55833 |
rs539943607 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931081 | TGAAATATTATGAAC[A/C]AACAGTTGACCCCTG | 55833 |
rs539947385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014368 | AGGTGCGGTGGCTCA[C/T]GCCTATAATCACAGC | 55833 |
rs539960852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981255 | TTCTGGATATATATA[C/T]ATATTCTGGATATAT | 55833 |
rs539960969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974389 | GTACATGCCTGTAGT[A/C]CCAACTACTCGGAAG | 55833 |
rs540001313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960054 | CCTGCCTTAGCCTCC[C/T]GAGTAGCTGAGACTA | 55833 |
rs540007571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002401 | TTTTTTTTTTTGAGA[C/T]AGAGTCTCGCTCTGT | 55833 |
rs540039525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990799 | ACACCACCACACCCA[A/G]TGAATTTTTGTAATT | 55833 |
rs540041037 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946419 | TGTTTAACTATCTGA[C/T]CCACTGGCATTTTGG | 55833 |
rs540049969 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961468 | TCAGTACACAGGATG[C/T]GCTCAAACAGTTCTT | 55833 |
rs540072383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008409 | CCTTTGAACCAGGAT[A/G]GTGTGTGGAAGCAAT | 55833 |
rs540095224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002071 | AAGCACTCCTCTGAC[A/C]TCAGCCTCCTGAGTA | 55833 |
rs540111253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008627 | TCTGGACTGCAAAGC[A/G]TAAGATATATACTAA | 55833 |
rs540116032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995171 | AGACCAGTCTGGCCA[A/C]CATGGCGAAACCCCA | 55833 |
rs540155082 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017891 | GAGATCGCGTCACTG[C/T]ACTCCAGCCTTGGCG | 55833 |
rs540165194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954010 | CTCCCAGGCTTAAGC[A/G]ATTCTCGTGCCTCAG | 55833 |
rs540167513 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968588 | ACTGTTTGTTTTAAT[A/C]ATGAACGAATATTGA | 55833 |
rs540238739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929527 | AAGATTTCCTTTATG[C/T]ATTGATGGAGAGTGG | 55833 |
rs540240152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937262 | GTTCAATTTAACTGC[A/G]TCTGGGGTGTAAATA | 55833 |
rs540264404 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037557 | AATACATATTTTTAG[A/G]CTTTCCAAAAGCCCC | 55833 |
rs540267199 | snp | C/T | 3.29489e-05 | 0.00405874 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986774 | CCTCTACCCCGGGCT[C/T]GCTTGCCACGATCTG | 55833 |
rs540300754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973008 | AAACCCTGCTCTAAT[A/G]CCTGTTTAAAAGATC | 55833 |
rs540325645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021839 | GGGTCTCAACTTGTT[C/G]GTCAGGCTGGTTTCG | 55833 |
rs540359364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930572 | TGTACATAAAATACT[C/T]TCATTTATGTAACAA | 55833 |
rs540402819 | in-del | -/T | 0.246485 | 0.249975 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020826 | ACCAAGCCCAGCTAA[-/T]TTTTTTTGTATTTTT | 55833 |
rs540413044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951820 | CTTATCAATTCAGTG[C/G]ACACACATAGATTTC | 55833 |
rs540420405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968048 | CAAATCCAGTATCCA[C/T]TGATTTCTTCTCAAA | 55833 |
rs540424104 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038239 | GAAGATCATGAGGTC[A/T]GGAGTTCAAGACCAG | 55833 |
rs540426282 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013793 | GAGGCAGGAGAATCG[C/G]TTGGACCCAGGAGGC | 55833 |
rs540434448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925364 | CACTTTCACAGAACA[C/T]GAGAATTCTCCAGGC | 55833 |
rs540438753 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035977 | GCATCACTGCATTCC[C/T]GAGTGACAGAGTAAG | 55833 |
rs540441030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992771 | TGCAAAGTATACACA[A/C]ATGCATACTTTAAAA | 55833 |
rs540448120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044603 | GGTGTGGTGGCTCAC[A/G]CAAGTAATCCCAGCA | 55833 |
rs540452823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014993 | ACACTAACTTTATAC[G/T]GAAAAATGTAACGCA | 55833 |
rs540455784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958607 | GAGACACGGTTTCAC[C/T]ACGTTGGCCAGGCTT | 55833 |
rs540523139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936423 | CTCAGCCTCCCAAGT[A/G]GCTGGGATTACAGGC | 55833 |
rs540551484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986186 | GCCTCTCAAGTAGCT[A/G]GGACTACAGGTGCGT | 55833 |
rs540566168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045896 | GGTGATATTCCCTAC[A/G]TGTCCTCCCTCTCTT | 55833 |
rs540566743 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940486 | TGTCAAGTGATAAAA[-/G]GAACAAAGAGCCCAG | 55833 |
rs540572949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952630 | ATTGGAAAACAAGAA[A/G]TTGAATATACTAACT | 55833 |
rs540581209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047337 | AAGCCTTCAAAGCAA[A/T]GGAAGGACAACCCTA | 55833 |
rs540618358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943911 | GTCTCATTTAAAAAA[A/G]AAAAGGAGAAATTAA | 55833 |
rs540626121 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975553 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGA | 55833 |
rs540628993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927364 | GAGCAAAGAGAAATA[C/T]AAAAAGAATCTGCCT | 55833 |
rs540656194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020165 | TAAAAAAAAAAAAAA[A/C]AAAAAACTAAGAGAT | 55833 |
rs540688148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006644 | GCATGACCGTGCCAC[C/T]GCACTCCAGTCTGGG | 55833 |
rs540689666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001467 | AAAACTAGACTTAGA[A/G]TCACAAGAGTTCATC | 55833 |
rs540749091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005889 | CCTTGAGAATATCAA[A/T]CCCTAAATAATCAGT | 55833 |
rs540758425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048047 | CCAGAGTGGTGACAG[C/T]TGAGATGCGTGGGCA | 55833 |
rs540758876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968632 | CTGAAATAATCATAC[A/G]GATTTTTCTCCTTAA | 55833 |
rs540785095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042133 | GACTGAAAATGGGCA[C/G]TATTAAACCATATGT | 55833 |
rs540794675 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993928 | GAGACCGAGTCTCGC[A/T]CTGTCGCCTGGGCTG | 55833 |
rs540809017 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967868 | ATAGGTCAGCAGGAG[-/A]AAAAAATACTGTGAT | 55833 |
rs540813915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948862 | AATTTTTAAAAACGT[C/G]ATGTTGGCCGGGCGC | 55833 |
rs540841825 | in-del | -/AA | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017016 | TAAAAGAAAAAAAAG[-/AA]GAAAAAAAAAAAAAG | 55833 |
rs540844511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048609 | GTAGGAAGAAGCACA[A/G]GGCAACGTGAGGGGA | 55833 |
rs540846683 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953134 | CCCAGCTCCCAAAGT[A/G]CTGGGATTACAGGCA | 55833 |
rs540873405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000482 | TATTACAACAGGGAA[A/G]TTAGGTGAGGAATAT | 55833 |
rs540878937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941396 | GTACCCAGTACTACA[A/G]CCAAAGTGCTCATAC | 55833 |
rs540902733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993374 | TAGCCATAGGTGCTG[C/T]AGATGGCAACTAGGT | 55833 |
rs540906979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032831 | CCAGAGGCTGGGGCA[C/T]GAGAATCACTTGAAC | 55833 |
rs540941589 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020809 | GGACTACAGGCACCC[A/G]CCACCAAGCCCAGCT | 55833 |
rs540952210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030250 | GGAGATCGAGACCAC[C/T]CTGGCTAACACGGTG | 55833 |
rs540971759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032079 | GATCCCAGGATTTCG[A/G]GGCTACAGTGAGCTA | 55833 |
rs540993858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995312 | CAGTGAGTCAAGATC[A/G]CACTACTGCACTCCA | 55833 |
rs541010932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961210 | AAGAAAAGTATGGAT[A/G]TAGCACAAATATAGA | 55833 |
rs541011467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036337 | GGTCAGGATGGTCTC[A/G]AACTCCCGACCTCAG | 55833 |
rs541030571 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994383 | AAAAATAGTGTCTGG[A/G]CTTATCTCTACCATA | 55833 |
rs541057952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009616 | GCACTTATCCTACCA[C/T]ACAGTATAAGAAGTT | 55833 |
rs541061492 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977284 | CCTCGTGATCCGCCC[A/G]CCTTAGCCTCCCAAA | 55833 |
rs541085291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039315 | CTTCTGGGAAGTGAG[A/G]AGCCCCTCTGCCCGG | 55833 |
rs541109883 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028561 | ATTTTTTGTATTTTT[C/G]GTAGAGATGGGGTTC | 55833 |
rs541150319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034857 | CAGCCTGGGAAACAG[A/C]GAGACTCAATCTCAA | 55833 |
rs541159818 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025732 | TAACTGCCTAAAAAG[C/T]TTTGTTTCCGTTTTT | 55833 |
rs541178502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035963 | CAGTGAGCCTGATCG[C/T]ATCACTGCATTCCTG | 55833 |
rs541186679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989492 | AGGCGTGAGCCACCG[C/T]GCCCGGCACATGCAC | 55833 |
rs541197422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029047 | CTTGAGCTTAGGAGA[G/T]CAAGGCTGCAGTGTG | 55833 |
rs541201372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022694 | TCCACCAGCCTCAGC[C/T]TCCAAAGTGCTGGGA | 55833 |
rs541205216 | snp | A/C | 0.000133681 | 0.00817451 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956193 | TCTACATACTACTAA[A/C]CCCAAAACACTGACT | 55833 |
rs541210862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997811 | TATATCTCAAACTGT[A/G]TGAAGATCTCATTCC | 55833 |
rs541212273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040566 | GCCCAGCCAACATAG[C/T]GATACACTCTAATTA | 55833 |
rs541220066 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982748 | ACTTTTATTTATTTG[C/G]GGTTTATTAGTCTAA | 55833 |
rs541246103 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010031 | AGGCTGGTCTCAAAC[C/T]CCTGACCTCAGGTGA | 55833 |
rs541274145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997041 | CTGTCTCCCCCCTCA[A/G]AAAAAAGAAGAAAAA | 55833 |
rs541274174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004608 | TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 55833 |
rs541280699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939610 | AAAAAAATTAGCCAG[A/G]TATGGTGGCATGTGT | 55833 |
rs541304230 | in-del | -/AAA | 0.472052 | 0.11486 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010428 | GAAACTCTGCCTCAT[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs541305382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988811 | ATGAGCATACTATGG[A/G]CTAATCTTTCAGTCG | 55833 |
rs541319250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023980 | ACCTGGGAGGCGGAG[C/T]CTGCAGGGAGCCGAG | 55833 |
rs541387259 | snp | A/G | 1.69801e-05 | 0.00291372 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932626 | TGGTGGCTGGAGAGC[A/G]AACTAGAAGACAAAA | 55833 |
rs541454840 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046425 | GAGGCAGGCGGATCA[C/T]GGGGTCAGGAGATCA | 55833 |
rs541466471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938842 | ATTTCCATAGTTCAC[A/G]TGGTTTTTCTTGTTT | 55833 |
rs541475041 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977908 | TAGTCCCAGCTTCTC[A/G]GGAGGCTGAGGCAGG | 55833 |
rs541494247 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961054 | CGGTAAAATCAGTAA[G/T]ATTTCTTTTCTCCCC | 55833 |
rs541542139 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001793 | TGTACCATACCAGCA[A/G]ATTCAGGTAGCCTTG | 55833 |
rs541557822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034308 | CTCATGAATCCAGGA[C/T]ATCAAGTCCTGGTTT | 55833 |
rs541568432 | in-del | -/AAAT | 0.359575 | 0.224707 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962645 | AAGACTCTATCTCAA[-/AAAT]AAATAAATAAATAAA | 55833 |
rs541586052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946463 | CTTCATTTTTCAAAC[A/G]GTTTTAATAAAGCGT | 55833 |
rs541608834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955138 | ATCTAAATAAATGGT[A/G]CATGAAGAAACCAAA | 55833 |
rs541611787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047944 | AACAATATCCAATAG[A/C]AGTGGTAGTAAATGA | 55833 |
rs541652085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982307 | AGCTTATGAAAGATA[C/T]ACTCTATAGGAATGA | 55833 |
rs541655679 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016675 | ATTCTCCTGCCTTAG[C/T]CTCCCGAGAAGCTAG | 55833 |
rs541710600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016861 | CCGCACCCGGCCATC[A/G]CCTACTGTTTAAACA | 55833 |
rs541762105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976605 | ATGTTCTAAAATTGA[C/T]TGTGGTGATGATTGC | 55833 |
rs541804451 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968647 | GGATTTTTCTCCTTA[A/G]TTTTGTTAAATGGAT | 55833 |
rs541807413 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041279 | CCAACATAGTGAACC[C/G]ACAGCTCTACTAAAA | 55833 |
rs541837436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015996 | TAAAGTCTATTGTAA[G/T]TCAGGTATTTTACTA | 55833 |
rs541840469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952755 | TGACAAACCATAAAA[A/G]AATTTTTATCTTTGT | 55833 |
rs541847389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975768 | GATCACAACACTGCA[A/C]TCCAGCCTGGACAAC | 55833 |
rs541903143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009519 | CCCACCTCAGCCTCC[C/T]AAAGTGTTGAGATTA | 55833 |
rs541906357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033848 | TCAAGCAATTCTCCT[G/T]TCTCAGCCTCCCAAG | 55833 |
rs541915286 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987340 | TTGCTTGGACCCAAC[A/T]GGCGGAGGTTGCAGT | 55833 |
rs541922169 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030478 | AAACAAAAAAACTGG[C/T]CCGGTATGACAGAGC | 55833 |
rs541978364 | snp | C/T | 1.64795e-05 | 0.00287045 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33996316 | TTCATCCTGATTTTT[C/T]CCTGTCACTTCCATA | 55833 |
rs542021402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047220 | GTGGGAAAATCTCTC[C/G]TCACACGTATCAACT | 55833 |
rs542037057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937998 | GGGGGGTTTCTTTTG[A/T]TTTTTTGTTTTTGTT | 55833 |
rs542038710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946363 | AACAACAAAAAAATT[A/C]TCCTGTGTTTTCTCT | 55833 |
rs542071358 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957841 | AGGTAGAGGAGACAG[G/T]AGGTGTTCATTTTCT | 55833 |
rs542075830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931944 | TCTCTTAAGTTTTCA[C/T]TGCATGCCCTCTACA | 55833 |
rs542088974 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003258 | CTGGTCTTGAACGTC[A/T]GACCTCGAGTGATCT | 55833 |
rs542105942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995218 | AAAAATTAGCTGGTC[A/G]TGGTGGCGCATGCCT | 55833 |
rs542132150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035922 | TGAGTGGGGGAAATC[A/G]CTTGAGCCCAGGTAG | 55833 |
rs542142661 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982970 | CAGCAACCTCCGCCT[C/T]CCAGGTTCAAGCAAT | 55833 |
rs542147818 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955649 | GCCTGACCAACATGG[A/T]AAAACTGTCTCTACT | 55833 |
rs542161313 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931393 | CTGTGGCAGGCTGGA[A/C/G]TACATGGTCTGGAGG | 55833 |
rs542170253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045741 | ACTCAGCAGGAAATA[C/T]CAGCATAAGTGGTTT | 55833 |
rs542202728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938721 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGG | 55833 |
rs542218848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043030 | CCATGATCATGCCAA[A/G]ACACTCCATCCTGGG | 55833 |
rs542257002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005078 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 55833 |
rs542265550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945395 | TCCCAGCTACTCGGG[A/G]GGCTGAGGCAGGCCC | 55833 |
rs542270072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043964 | AAAATCCTGTCTCTA[C/T]AAAAAATACGAAAAT | 55833 |
rs542276488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943194 | CCAAGATTCCAGTTA[C/T]ATGAAATGTCCAGGT | 55833 |
rs542293928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994175 | CTGGGATTACAGGCA[C/T]GAGCCGCAGTGCCCA | 55833 |
rs542301855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030697 | TTTGGGAGGCCCGGG[C/T]GCATGGATCACAAGG | 55833 |
rs542341400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991180 | AATCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA | 55833 |
rs542357715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039254 | CGCCTCCGCCTGGCC[A/G]CCGCCCCGTCCGAGA | 55833 |
rs542387594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025416 | CTATCTCAAGTTCTT[A/G]AGGGGCAGGAAGCAC | 55833 |
rs542401117 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927173 | CACAGTCACTGAGCT[A/G]CCCCAGATGGGTTCA | 55833 |
rs542403442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981551 | AAACAAAAAAAGCCT[G/T]CTACATTGTCCACTC | 55833 |
rs542405094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037040 | ATCACCCGGGCTGGA[A/G]TGCAGTGGCACAATC | 55833 |
rs542411004 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972909 | GAGAAGAGAGATGTT[C/G]CTAAGCAACCTACAA | 55833 |
rs542474436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934966 | ACTGAGGCTCACCTC[A/G]GTCTGCTTAAGTTCA | 55833 |
rs542487386 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987335 | GAGAATTGCTTGGAC[A/C]CAACAGGCGGAGGTT | 55833 |
rs542500645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022575 | CAAGTAGCTGGGACT[A/G]TAGGTATGTGCCACC | 55833 |
rs542506382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929027 | GTTTCCTGGGGCTCC[A/G]AGGCGTCTTGTTCCT | 55833 |
rs542541157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928654 | TGCTCCATCAGCCCC[A/G]AGTCCCAGAAGCCCT | 55833 |
rs542552898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019608 | CAGTGGTGGTTGCAC[A/G]ACAATGTAAATGTAC | 55833 |
rs542602671 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995862 | TGGTTTTCTGTTATA[A/C]TAGAGATGTAAGAAG | 55833 |
rs542628743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949617 | CTGAGACAGGAGAAT[C/G]GCTTGAACCCAGGAA | 55833 |
rs542640527 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034804 | CTTCAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55833 |
rs542652080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998001 | TCAGCAAAGAAGAGT[C/T]AGAAATTAAGACTAA | 55833 |
rs542659581 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049182 | AACTGCAGCTCGTCG[C/T]CGCGCCGTGATGACC | 55833 |
rs542673409 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940754 | ACTGGACTCTAACCT[C/G]GGTGACAAAGCAAGA | 55833 |
rs542700092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989436 | TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT | 55833 |
rs542721108 | in-del | -/A | 0.117188 | 0.211804 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976262 | TAAAACCTTGAACTG[-/A]AAAAAAAAATGCAGT | 55833 |
rs542733481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977376 | AAAATCTAATCCATC[G/T]TCCCCATAAATTCTA | 55833 |
rs542733535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983851 | ACAGAATTATACTTG[C/G]TTTTTACCAATTTAC | 55833 |
rs542784431 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974489 | TCTAGTCAGTGTGAC[-/AG]AGTGAGACCATTTCT | 55833 |
rs542790464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950142 | GCGATCTCGGCTCAC[C/T]GCAAGCTCCGCCTCC | 55833 |
rs542800512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985112 | CAATCCCATTAGCAG[A/G]TATTTATACAAAGAA | 55833 |
rs542846946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971176 | TAACCAATATTTACC[C/T]CAAGAATTTCAGAAA | 55833 |
rs542868290 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012006 | TAAACATTAACAGTC[G/T]ACTAAGCCTGTACTC | 55833 |
rs542868563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004653 | GCCGAGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 55833 |
rs542880533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960502 | AGGTATCGGCCAGGC[A/G]CAGTGTCTCACGCCT | 55833 |
rs542885945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018051 | TTCTAAGCTGGGCAC[A/G]GTGGCATGCACCTGC | 55833 |
rs542888214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984656 | GCACTCCAGCCTGGG[C/G]AACAGAGTGAGACAC | 55833 |
rs542919937 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040950 | ACTTAGTAAAAGTTA[C/T]ACATACCCTACATAC | 55833 |
rs542931612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011087 | AAGAAACACCGACCC[A/G]ATTAAAATATTAACA | 55833 |
rs542962154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979284 | TTGACTCAATCTCAC[C/G]AAAAGACCAAAATAA | 55833 |
rs543003537 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999859 | GGATTACTACGTATG[C/T]ATGTATGTATGTATG | 55833 |
rs543012345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048663 | TGGACGTAGAGGGAC[C/T]GTGGACCTGGCGAGT | 55833 |
rs543026732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004636 | AAAAATACAAAAAAT[C/T]AGCCGAGCGTGGTGG | 55833 |
rs543054495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011052 | CAGTGCTTTGTAAAC[A/G]TGCACAATTTACAAA | 55833 |
rs543087600 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950135 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 55833 |
rs543091330 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036359 | CGACCTCAGGTGATC[C/T]GCCCGTCTCGGCCTC | 55833 |
rs543104188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017621 | GTCAGCTGTAAATAA[C/T]AAATCTTAAAGAAAC | 55833 |
rs543114700 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997893 | GACCTTTACTCCAAA[C/G]AACAATTATTAGACG | 55833 |
rs543118136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024027 | CCAGTCCGGGTGACA[A/G]AGCAAGACTCTGTCT | 55833 |
rs543135280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927487 | GCTGGGCCTACAGAC[A/G]GCCTAGGTCTGCAGT | 55833 |
rs543152099 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042244 | CAGCACTTTGGGAGC[G/T]CAGGTGGGCGGATCA | 55833 |
rs543153834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030217 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACGGGGT | 55833 |
rs543177285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036940 | TCCCGCCTCAGCCTC[C/T]CAAGTAGGTGGGACT | 55833 |
rs543209352 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921226 | ACCCTCACTAGTCAC[A/G]TGTTCTACCATAGCT | 55833 |
rs543215584 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050434 | GGTCTAAGTAAGGTA[C/G]AAAGGGGAAATTAGC | 55833 |
rs543236592 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975257 | CAATATGGTGAAACC[C/T]CGTCTTTATTAAAAA | 55833 |
rs543242197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970558 | ACTTCAGCCTCCCAA[A/G]CAGCTGGGACCACAG | 55833 |
rs543242799 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001649 | CAAGATAACTCCAAT[C/T]CATATAATCAATTTT | 55833 |
rs543255350 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025902 | TGTTTTTTTCAAGGA[C/T]CTTTCTGAAGATAAG | 55833 |
rs543274661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964006 | AATCACTTCAATTAT[C/T]CTCATTCTCACGCCC | 55833 |
rs543296377 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040674 | AACATCCCACTACAA[C/T]TGGCTAAAACTAAAA | 55833 |
rs543376691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988887 | CAGTGACTCATGCCT[A/G]TAATCCCAAAACTTT | 55833 |
rs543400237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955716 | CTGTAATCCCAGCTA[C/T]CTGGGAGGCTTGAGG | 55833 |
rs543411844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996100 | GTTCTTTCTGGAACT[G/T]AAAACAAATATGGAA | 55833 |
rs543416721 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921862 | TTTTTTTTTTTTCAT[G/T]GTCAGCCAGTCTCTA | 55833 |
rs543429770 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947834 | TGACTCAAAAAAAAA[A/T]AAAATAAAATAATAG | 55833 |
rs543445390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003973 | GATCCGCCCACCTCG[C/G]CCTCCCAAAGTGCTG | 55833 |
rs543469158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971093 | CAGGTGTGAGCCACC[A/G]CGCCCAGCTAAATTA | 55833 |
rs543471345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962275 | CTATATGTACAGTTA[A/C]TGTAGTAAGTTAAAA | 55833 |
rs543487387 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989413 | TCATCGTGTTAGCCA[G/T]GATGGTCTCGATCTC | 55833 |
rs543526196 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924591 | ATGCCTCGGGCTGAA[A/C]CAACTTCGCTGGCTT | 55833 |
rs543545543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029805 | TCAGCCTGGCCAACA[G/T]GGTGAAAACCCATCT | 55833 |
rs543567302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030295 | CTAAAAATACAAAAA[C/T]AAAATTAGCCAGGCG | 55833 |
rs543577127 | in-del | -/GCG | 0.00159617 | 0.0282053 | utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34048899 | TGTGCCTCTTACAAA[-/GCG]GCGGCGGCGGCGGCA | 55833 |
rs543582080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950068 | ATAACATTTCTTTTC[C/T]TTTCTTTTTTCTTTT | 55833 |
rs543603524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983988 | ACAATCTCGGCTCAC[C/T]GCAGCCTCCACTTCC | 55833 |
rs543604216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998572 | CTAGTAACTCAGAAA[G/T]ATTATATTGTAAGGC | 55833 |
rs543605090 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991060 | GAGGCCAAAGCAGGA[A/C]GATCACTTGAGGCCA | 55833 |
rs543658624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010451 | AAAAAAAAAAAAAAG[A/T]CAATAAACAAATAAT | 55833 |
rs543663662 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000215 | CAACTCCTGAGTTCA[A/G]GAGATCCTGCCGCCT | 55833 |
rs543685821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024001 | GGGAGCCGAGATGGC[A/G]CCATTGCACTCCAGT | 55833 |
rs543690578 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990601 | ATGCATCTATTGTAA[A/C]CTTTCTAGAAGGTTA | 55833 |
rs543694735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949553 | ACTAAAAATACAAAA[A/G]TTAGCCAGGGATGGT | 55833 |
rs543720647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017557 | GATTTTACCTGCCAA[C/T]AGCCCAATTTAAAAT | 55833 |
rs543742863 | in-del | -/AG | 0.0019972 | 0.0315375 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017460 | TTATCACTACATGTA[-/AG]GTCACTGTACATGAA | 55833 |
rs543754483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965786 | GGGTGCGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 55833 |
rs543762940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984513 | TAAAAAAAAAATTTT[C/T]TTTTTTCTTTAAATT | 55833 |
rs543765251 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986092 | GAGTCTTGCTCACTT[G/T]CCCAGGCTGGAGTGC | 55833 |
rs543797570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014187 | AAAAAGTTAGCCGGG[C/T]ATGGTGGCTCACGCC | 55833 |
rs543805339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034932 | CTACATCCGGATTAC[A/T]CTCAAAAACAAAGGC | 55833 |
rs543902278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029221 | AGAGAACTGAAAACA[C/T]GTTCACCTAAAAATG | 55833 |
rs543918518 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018231 | GATAGCGATTACAAT[-/T]TTTTTTTTTTTTTTT | 55833 |
rs543923161 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018307 | TAGACAAATTCTAAA[A/G]GAGCTGTAACACTAT | 55833 |
rs543927807 | snp | C/T | 0.000675392 | 0.0183641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986711 | CAACGCAACTGCCTG[C/T]TTCTTCCCCCTAATT | 55833 |
rs544019502 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926875 | GACGGGGGTGCTCAG[A/G]GATGGAAGGGCAGCT | 55833 |
rs544037129 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980600 | CAAAAAATGGATCTA[C/T]GTCAAGTACATTAAG | 55833 |
rs544065331 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018724 | AAAAATTAGCCAGGC[A/G]TAGTGGCGGGCGACT | 55833 |
rs544079447 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040023 | TTAGCCGGGGGCATG[A/G]TGGCACATGCCTGTA | 55833 |
rs544146872 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976290 | AGTATATTCATACAA[C/T]ATTATATTATATTGC | 55833 |
rs544150987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967845 | TGTCACTCAACATCA[C/T]TGATGTCAATAGGTC | 55833 |
rs544234656 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004439 | GCAGTGAGCCAAGAT[C/G]GCGCCACTGCACTCC | 55833 |
rs544280573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929828 | TCAACACAGTGAAAC[C/T]CTGCCTCTATTAAAA | 55833 |
rs544282442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937152 | AAAAAAAAAAGTGAA[A/C]ATTATATTGCATGGT | 55833 |
rs544300009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928610 | CTGTTTGACAAGGTA[C/T]CCCTGTGAAGAAAGA | 55833 |
rs544316468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978707 | ATGGCGTGAACCCAG[A/G]AGGGGGAGCGTGCAA | 55833 |
rs544334440 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938091 | CAACCTCCGCTTCCT[A/G]GTTCAAGCCATCCTC | 55833 |
rs544367310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936356 | CTGGAGTGCAATGGC[A/G]CATCTTAGATCACTG | 55833 |
rs544393489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974342 | CAAAACCTTGTCTCT[A/G]CAAAAAATACAAATA | 55833 |
rs544395566 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016309 | GAAGAGGAGGAAGAG[A/G]AGGAAGAGAAGGAGG | 55833 |
rs544425542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021096 | TATTTTTGATCTGTG[C/T]ATCATAAAATAAAAT | 55833 |
rs544430815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964725 | TCTTAAAAAAAAAAG[A/C]AGCAAGAAAAAAAAA | 55833 |
rs544430884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043973 | TCTCTACAAAAAATA[C/T]GAAAATTATCAGAGC | 55833 |
rs544487940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992160 | TTTGGGAGGCTGAGC[A/G]GGTGGATCACCTGAG | 55833 |
rs544489559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958870 | AAATTAAAAAAAGGC[C/T]GGGCGCAGTGGCTCA | 55833 |
rs544504564 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050162 | TAGGAGTAGCTGCAC[G/T]CCCGTGTTAACAAGC | 55833 |
rs544506393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957888 | GCTAAATTGTTTACC[A/G]GTTCAACAAGTCAAC | 55833 |
rs544568858 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969453 | AGTACTAGGGAGATT[A/T]AGGTGGGATGGCTTG | 55833 |
rs544569784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992010 | TGTAATCCCAGCACT[C/T]TGGGAGCCCAAGGTG | 55833 |
rs544584196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951012 | TCACTTCTGTTGCTG[C/T]TGTTATTTACTAGGT | 55833 |
rs544625680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025883 | CCATGCCCGGTTTAA[A/C]TGCTGTTTTTTTCAA | 55833 |
rs544630357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993642 | CTGCACTCTAGCCTG[A/G]GCAACGGAGTGAGAC | 55833 |
rs544645843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037783 | TAAATACACAAACCC[C/T]GACTGGATGGGAAAA | 55833 |
rs544648665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018793 | GCGTGAACCCGGGAG[A/G]TGGAGCTTGCAGTGA | 55833 |
rs544651555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999417 | AAGGTAATGCAAACA[A/G]CTGCCCAGACACAGG | 55833 |
rs544662295 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937132 | ACTGGTGGTGATTCA[-/A]AAAAAAAAAAAAAAG | 55833 |
rs544682197 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992660 | ACTTATCGGGCGGAG[C/G]GGGGGGGGCACAAAT | 55833 |
rs544687556 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009262 | CACCACCACGGCCAG[C/T]TAATTTTTCTATTTT | 55833 |
rs544696098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025988 | AATGGTTGACTTAAC[A/C]ACCACCAACATTTCT | 55833 |
rs544705455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019410 | TCTCGGGGCAAGGGG[A/T]AAAAAAAAACGGACA | 55833 |
rs544707568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972899 | TAATAGTACAGAGAA[C/G]AGAGATGTTGCTAAG | 55833 |
rs544739858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935574 | GCCTGGCCCAAGCAT[C/G]TTTAAAATGCATACT | 55833 |
rs544752230 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941974 | CATCAATTTATTATC[C/T]CAAATGAGACCCACC | 55833 |
rs544752688 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050863 | TTAGCCGGGCGTGGT[A/G]GCGGGCGCCTGTAGT | 55833 |
rs544769179 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044530 | AGGCACCACAGCACT[A/C]CAGCCTGGGCGACAG | 55833 |
rs544848249 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942728 | GCAAGACCCTATCTC[-/AAAA]AAAAAAAAAAGAAAA | 55833 |
rs544870022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043364 | TAAAGACAGGGTTTT[A/G]CCACGTTGTCTAAGC | 55833 |
rs544896643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038399 | CTGATTCTCCTGCCT[C/T]GGCCTGCCAAGTGCC | 55833 |
rs544900330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020998 | ACCCAAAAGCAAGCA[C/T]TCCCATGATGTGGAA | 55833 |
rs544912332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020278 | AGGTCTTCAGCGCAA[C/T]AACACATAGAGCTAT | 55833 |
rs544913471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979533 | TGAGCCAAGATCCCA[C/T]CATCGCACTCCAGCC | 55833 |
rs544925444 | in-del | -/T | 0.112983 | 0.209108 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982880 | TGGTGTTTTTTTTTG[-/T]TTTTTTTTTTTTTGT | 55833 |
rs544957562 | snp | A/T | 0.182296 | 0.240658 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978017 | GAGACTCTGTCTTTT[A/T]AAAAAAAAAAAAAAA | 55833 |
rs545014474 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960941 | CAGTCTCAGTCCAAA[C/T]GATTCCTTTTTGTGT | 55833 |
rs545087567 | snp | C/T | 0.000133376 | 0.00816517 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943608 | AAAAAGCAAAGCTGT[C/T]GTGTCAGGAACAGAG | 55833 |
rs545115836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971283 | ACATTATCATACATT[A/G]TCTGGCCAAAGAATC | 55833 |
rs545163121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943068 | ATGAATGAATAAAAT[A/G]TGGTATTATCAACAC | 55833 |
rs545194877 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991602 | AGTCATTATTTAAGT[A/G]AGGATGTTTAATTTG | 55833 |
rs545201352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936314 | AAAGGTAACTTTTTG[A/G]GATGGTGTCTTGCGC | 55833 |
rs545220159 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929902 | CCAGCTACTAGGGAG[A/G]CTGAGGCAGGAGAAC | 55833 |
rs545229990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985894 | GGGCATGGTGGCGTG[C/T]ACCTGTAGTCCCAGC | 55833 |
rs545256218 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019394 | GGCGACAGAGCAAAA[C/T]TCTCGGGGCAAGGGG | 55833 |
rs545275852 | in-del | -/GAA | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939957 | AAAGAGGGAAGGAAG[-/GAA]GAAGAAGAAAAAATA | 55833 |
rs545281525 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927419 | TGCAGTGCCAGGAGA[A/G]GGACAGGCTGAGTTC | 55833 |
rs545283313 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967801 | ACTGGAGTATATTTT[A/C]TTTAAAAAATGAAAA | 55833 |
rs545315415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012328 | CTAAGGTCAGGAGTT[C/T]GAGAGCAGCCTGGCC | 55833 |
rs545341506 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973490 | TGACAGCTAAACACA[C/G]GGAGGTTGTATTATA | 55833 |
rs545379743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957034 | GTTGAGGCTGCCGTG[A/G]GCCATGATCACACCA | 55833 |
rs545400042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005098 | TGAAACCCCGTCTAC[A/C]CTAAAAATACAAAAA | 55833 |
rs545428615 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982003 | GGATACTGGTGAGAA[C/G]AACAGAATTGTTAAG | 55833 |
rs545439743 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972442 | CTTTTCCTCAAAGGA[A/G]CTTAGGCAGAAGGCA | 55833 |
rs545458989 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001041 | AATCATAACCAACCA[A/G]TAAGTCCCAGTGCCA | 55833 |
rs545475402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928470 | CCTTCTATTGGGATT[C/T]TCAGCCACTGTGGTC | 55833 |
rs545511060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968203 | ATTTGGTGCATTCGA[C/T]TGGTACAGGATTATG | 55833 |
rs545517576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018779 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGT | 55833 |
rs545550342 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969867 | ACCCCACCTCAAACA[A/C/T]CCCCCCACCCCCAAA | 55833 |
rs545558793 | in-del | -/GGAA/GGAAGGAAGGAA | 0.0440565 | 0.142831 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981859 | AAGGGAGGGAGGGAA[-/GGAA/GGAAGGAAGGAA]GGAAGGAAGGAAGGA | 55833 |
rs545577898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926245 | GAAGAGGAAGACAGT[A/G]TAAAACTCCAGGGCC | 55833 |
rs545586455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960340 | AATCTGAAAATCTAA[G/T]TTCCTTTTAAGAAGC | 55833 |
rs545613488 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048083 | TAGACTAAAAACTCA[-/G]GGGGAAAATGTGGAA | 55833 |
rs545623485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968609 | CGAATATTGAACACT[C/T]TTCCTTACTGAAATA | 55833 |
rs545679181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950161 | AGCTCCGCCTCCCAG[G/T]TTCACTCCATTCTCC | 55833 |
rs545687413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964638 | CCAGGAGTTTGAGGT[C/T]GTAGTGCACTAAGAT | 55833 |
rs545692957 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33960876 | CAGAATTCTTCCAAG[C/T]CCCTGTTGGGAAACA | 55833 |
rs545697281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043921 | TCACCTGAGGTCAGG[A/G]GTTCAAAACCAGCAT | 55833 |
rs545728405 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050068 | TCCTCCCGCACCTCT[A/C]CATGTGCGTCCCTCC | 55833 |
rs545743510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33954953 | TTTGAAACCACTTTC[A/G]AAGGTGTTTAGTGTG | 55833 |
rs545776134 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995229 | GGTCGTGGTGGCGCA[G/T]GCCTGTAGTACTAGC | 55833 |
rs545808416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931146 | CAGGCAGATTTCTTT[C/T]TCAACCCAATGCACG | 55833 |
rs545822402 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981461 | CCCAGACTCAAGCCA[A/T]CCTACCACCTCAGCC | 55833 |
rs545837762 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982512 | TAAAATTAAGTGCCC[A/G]TTTTGTCGCCCAGAT | 55833 |
rs545837770 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955713 | TGCCTGTAATCCCAG[C/G]TACCTGGGAGGCTTG | 55833 |
rs545866073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958231 | CCTCCCAAAGTGCTA[C/G]GGTTACAGGCATGAG | 55833 |
rs545866519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015835 | CATCATGCCCAGCTA[C/T]TTTTTAAACTTTTTG | 55833 |
rs545871214 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038808 | GTGAGGAGCGCCTCT[G/T]CCTGGCCGCCATCCC | 55833 |
rs545880411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924674 | TGAAAAAGGAGGCAA[C/G]AGAAGTGCAGGGGCC | 55833 |
rs545929794 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022472 | AGACACAGTCTGGCT[C/T]TGTTGCCCAGGCTGG | 55833 |
rs545929831 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015117 | GTATAGTCAAATCAA[C/T]CTGCAAGTAAGACAA | 55833 |
rs545934539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045203 | TACAAAAAATTAGCC[A/G]GGCGTGGCGGCAGGC | 55833 |
rs545948959 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940414 | TACTCAGAAACCTTG[A/G]ACATACAGAGTTGTT | 55833 |
rs545954693 | snp | A/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002628 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 55833 |
rs545955501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039208 | GGGGCAGCCCCCGCC[C/T]GGCCAGCCGCCCCGT | 55833 |
rs545963764 | snp | A/T | 0.000399281 | 0.0141238 | missense | UBAP2 | GRCh38.p7 | 9:33944632 | TGGCTCAGGTTGAGA[A/T]TTGAAGTCTAAAAAA | 55833 |
rs545992687 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935967 | CTACAACATGTAGCT[C/T]AATCAAGAAACAATT | 55833 |
rs546001479 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033173 | TCTGCATTCCTGTTT[C/G]TTGCAGCACTGTTTA | 55833 |
rs546014136 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970387 | TGCTTCTGGTGGTAC[C/T]CTCTTATTTTTTGGC | 55833 |
rs546018176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008770 | AAGAAATCGAGACCA[C/T]CCTGGCCAACATGGT | 55833 |
rs546044843 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946562 | GGGGCCAGATAGTAC[A/C]ACAACCTAATATTTT | 55833 |
rs546049382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937894 | GGCACTCCAGCCTGG[A/G]CAACAACAGCAAACC | 55833 |
rs546083557 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954388 | GAACTCTTAAAACAC[A/C]CCCCAGACAGATATT | 55833 |
rs546098865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040736 | ACTCTTAAACCACTC[A/G]GTCTTTGAGAATGAA | 55833 |
rs546122889 | snp | A/C/G | 3.29576e-05 | 0.00405928 | missense | UBAP2 | GRCh38.p7 | 9:33960871 | TTCCACAGAATTCTT[A/C/G]CAAGCCCCTGTTGGG | 55833 |
rs546126992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945324 | TAACATGGTGAAACC[C/T]CATCTCTACTAAAAA | 55833 |
rs546128295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001914 | AAAAATCCATAAAGT[C/G]ACCATCTAACACCAA | 55833 |
rs546135932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937349 | CAGTGGCTCACACCC[A/G]TAGTCCCAGCACTAT | 55833 |
rs546230927 | snp | A/G/T | 0.000280623 | 0.0118426 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973279 | TAAAATAATACTTAT[A/G/T]TCCTACACAATTACA | 55833 |
rs546231044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980256 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTT | 55833 |
rs546231628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965535 | ACCTAAAATCACTAG[A/G]ATTTGCCACTATATC | 55833 |
rs546240575 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042010 | GCCTGAGCAACAGAC[-/T]TGAGACCCTATCTCA | 55833 |
rs546244629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952704 | AGAAGAAAGGGGTAC[C/T]TTCAATCTCAAGAGT | 55833 |
rs546245443 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966131 | TACTTTAGTTCCTTT[A/G]ATATTATATAAAAAT | 55833 |
rs546254161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013288 | GCTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55833 |
rs546279403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958689 | CTGGATTACAGGCAT[A/G]AGCCACTGTGCCCGG | 55833 |
rs546287992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007040 | ATCCTGCAACTTCAC[C/T]GAATTCATTTCTCAG | 55833 |
rs546288480 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035410 | GGGAGGCTGAGGTGG[A/G]AGAACAGCTTGAACC | 55833 |
rs546362807 | in-del | -/T | 0.158257 | 0.232558 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984509 | TCTTAAAAAAAAAAT[-/T]TTTTTTTTTTCTTTA | 55833 |
rs546368508 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33933934 | AAAGGAACCTAAGCT[A/G]TAGATGCATCCAGAA | 55833 |
rs546384411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994017 | CTCCTGCCTCAGCCG[C/T]CTGAGTAGCTGGGAT | 55833 |
rs546422863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007619 | ATTGAAATGATCATA[C/T]GTTTTTTGTCCTTGT | 55833 |
rs546424889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000863 | CTATGCCTGCTGAGA[C/T]CTCAGTTTAACTGCT | 55833 |
rs546434015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038628 | GGCGTGATCTCGGCT[C/T]ACTACAACCTCCACC | 55833 |
rs546467688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027794 | TGAACCTGGGAGGCA[A/G]GAGCTTGCAGTGAGC | 55833 |
rs546497122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987282 | CCAAGTGTGGTGGCG[C/T]GCACCTATAGTCCCA | 55833 |
rs546545385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939135 | GTCTCATTAGAGGTA[A/G]AGTGGCATAATCTCA | 55833 |
rs546551083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020485 | ACGCGCCACCATGCC[C/T]GGCTAATTTTTGGTA | 55833 |
rs546602906 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935495 | TGGTCTCAAACTCCT[C/G]AGCTTGGGCAATCTG | 55833 |
rs546603513 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031323 | ACATGGCAAAACCCC[A/G]TCTCTACTGAAAATA | 55833 |
rs546631767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923666 | GTCCCCAGCCTGAAC[A/G]GTTTCTGAAGACCAG | 55833 |
rs546688050 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014629 | AGGAGACTCCATCTC[A/G]AAGAAACAAAAAAAA | 55833 |
rs546690198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966299 | CTAAAACTACAAAAA[A/C]AAAAAAAAAATTAGC | 55833 |
rs546701059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950533 | CATTAGGTTATGGAC[A/C]GCTGTGACAGAGATT | 55833 |
rs546758246 | snp | A/C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932360 | TGATTCTTCCCAGGC[A/C/G]CTACAAACTTAGAAA | 55833 |
rs546769597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991494 | ATAGAAAGAGGTCCT[G/T]GATAGAAAAAGCAAG | 55833 |
rs546790242 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011880 | GCTGCTTTCACAGTG[A/G]AAAATGTGAAATTTT | 55833 |
rs546799693 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958393 | CTAAACATGATAATA[A/C]AACACTGAATGGTTC | 55833 |
rs546805295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33952216 | GTAGTTCTGCATCCA[C/T]AGACCTTTCTAACTT | 55833 |
rs546810285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037462 | TAAGTTTTTACTAAT[A/G]TAATTGTTGCCTCAC | 55833 |
rs546837615 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037240 | TGATCCGCCCGCCTC[A/G]GCCCCCCAAAGTGCT | 55833 |
rs546855191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935258 | CTAAAGACAATGAGC[C/G]TATCTTTCCTGAACA | 55833 |
rs546864874 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993662 | CGGAGTGAGACCCTG[A/T]CTTAATAAAAAACCC | 55833 |
rs546881883 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984925 | GACTGCAATGAGTTA[C/T]GATCATGACACTGCA | 55833 |
rs546905897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038977 | CCCGACCGCGACCCC[A/G]TCTGGGAGTTGAGGA | 55833 |
rs546937119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005153 | CTGAAATCCCAACTA[C/G]TCAGGAGGTTGAGGC | 55833 |
rs546941032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046476 | GTGAAACCCCATCTC[C/T]ACTGAAAAATACAAA | 55833 |
rs546943738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040201 | TGGTGGCACGTGCCT[A/G]TAGTCCCAGCTACTA | 55833 |
rs547007579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964296 | GAAAAACAGCCAGCA[C/T]CATCAGCTGACATCC | 55833 |
rs547017254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953925 | TTTTTTTTTTTTTCT[A/G]AGACAGTGTCTCACT | 55833 |
rs547050864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005350 | TGAGGTGTGAGAATC[A/G]CTTGAACCTGGGAGG | 55833 |
rs547073171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999854 | AGCTGGGATTACTAC[A/G]TATGTATGTATGTAT | 55833 |
rs547155905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035231 | CATACGGCTAGGCGC[A/G]GTGGCTCACGCCTGT | 55833 |
rs547176867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992248 | ACAAAATTAGCCGGG[C/T]GTGGTGGCGCATTCC | 55833 |
rs547177488 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940179 | GCAGATTTAATATGG[G/T]AACCACCACAGTGTC | 55833 |
rs547215185 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983354 | GTGGGATTTCAGTCA[C/T]GAAGATTTGACGATT | 55833 |
rs547236562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030817 | CGCCTGTAGTCCCAA[C/T]AACCCAGAAGGCTGA | 55833 |
rs547242135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029379 | CTAAAAATATAAAAA[A/G]TTAGCTGGATGTGGT | 55833 |
rs547253313 | in-del | -/CAGTTCTTCCAC | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964531 | CACAGCTTCCACACA[-/CAGTTCTTCCAC]ACTGTGTGGAAGCTG | 55833 |
rs547265430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977035 | CAAAAACAGTTGTTT[C/T]TTATTTATTTTTTTT | 55833 |
rs547267346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929240 | TCTCGGAAGGAAAAA[G/T]GAACATTCTCCATCG | 55833 |
rs547295812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026957 | TCACCTGCAAAGCTT[A/G]TGCCTGATGACAAAG | 55833 |
rs547346427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027654 | TGAGGTCAAGAGATC[A/G]AGACCATCCTGGCTA | 55833 |
rs547395518 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028279 | TTCAGGTTACCTAAG[G/T]CCACGAAGGGAATTA | 55833 |
rs547432188 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050539 | AAACAGCCCTATCTA[A/G]TTCAAATAAAGCCTT | 55833 |
rs547438443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925248 | CTCCAGGAAACCTCC[C/T]GGAAACCCATAGCAG | 55833 |
rs547440036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987442 | TACAAAATACAAAAA[A/C]ATACAAAAATTATCC | 55833 |
rs547443113 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939334 | CCCAAGTAGTAGCTG[C/G]GACTACAGGCACGCA | 55833 |
rs547460574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988541 | AGTGTCTATAAATGG[A/C]GAATATAAAACAGCT | 55833 |
rs547470987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955343 | AGCCAATATGGTGAA[A/T]CCCCGTCTCCACTAA | 55833 |
rs547512160 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034619 | GTGGCTCACGCCTGT[A/C]ATCCCAGCACTTTGG | 55833 |
rs547531312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028108 | CTAGCAGCTGATGGA[C/G]AAGGTTGAACTCCCC | 55833 |
rs547537111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003457 | ACTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 55833 |
rs547542911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995799 | ATATTAAAAAAAAAA[A/G]AGAAAACTTAATATT | 55833 |
rs547570178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982565 | GATTGTTTGCATTCT[A/G]TTCCTATTCACCGGT | 55833 |
rs547600371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925612 | CGGCAGATTAAAGGG[C/G]TGCTGGTTTGCACAG | 55833 |
rs547635908 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029741 | ACACCTGTAAACCCA[C/G]CACTTTGGGAGGCCA | 55833 |
rs547649766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983423 | GAGATCAAATACCCT[A/G]GGAAAGAAAACCCTC | 55833 |
rs547675541 | snp | A/T | 0.000519337 | 0.0161059 | missense | UBAP2 | GRCh38.p7 | 9:33927065 | ACCCCCTGAGGTAAG[A/T]TTGGGGGTGCTTTGC | 55833 |
rs547709544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926369 | TTAACAGGGGACATG[G/T]CCTACCAGGGCCCCA | 55833 |
rs547714455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029980 | TGACAGAGCAAGACT[A/C]CATCTCGAAAAAAAA | 55833 |
rs547736225 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927451 | AAGTCGGTTTTAGCA[C/G]CGACCATCAAATCAT | 55833 |
rs547744998 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937496 | CCTGTAGTTCTAGCT[A/G]GTCGGGAGGCTGAGG | 55833 |
rs547771612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008942 | TGCACTCCAGCCTGG[C/T]GACACAGCGAGACTG | 55833 |
rs547788118 | in-del | -/CT | 0.00199208 | 0.0314971 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922491 | TGCCCCAGCCCACCC[-/CT]CTCTTCTGGGTTTAG | 55833 |
rs547791252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033294 | CATAAAAAAGAATGA[A/G]ATCCTGTCATTTGAA | 55833 |
rs547796659 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925858 | TGTCCAAACTGCCTG[C/T]AACTCTCTGACAAGT | 55833 |
rs547798211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945509 | AAACAAACAAACAAA[A/C]AACAAAATCCAATAG | 55833 |
rs547818561 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959130 | TCCAGCCTGGTGACA[C/G]AGCGAGAGCAAGGCC | 55833 |
rs547822605 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956261 | TCGCATAACAGCTAT[G/T]CTAAAGAAAATGAAA | 55833 |
rs547836571 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975096 | AATCCCATATTCATT[C/T]GGATGACTACTACCA | 55833 |
rs547889534 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953856 | GTTCCTAATAAATCC[A/G]TATTTCTAGGGAATG | 55833 |
rs547893087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974910 | GTCACTGTTCTCCAG[C/T]CTGGTTAACAGCGTG | 55833 |
rs547893123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981571 | ATTGTCCACTCTGAT[C/T]TTGAACTCCTGAGCT | 55833 |
rs547908426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968360 | ACACTTTGAGGTTCA[A/G]CAATAACATCATAAA | 55833 |
rs547908941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930839 | AAGTGGAGGTTGCAG[C/T]GAGCTGAGATTGCGC | 55833 |
rs547943212 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015318 | TAAAAATTTTATTCA[A/T]ATGGGTCTTTGTTTT | 55833 |
rs547950819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988388 | CTACACTGACACACT[G/T]CCAGAGCAGACAAGG | 55833 |
rs547964378 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955929 | TGATTGAAGCTCTGT[C/T]AGATTTACCAAGTAG | 55833 |
rs547966022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975943 | AATTGAGGCCTGACA[C/T]GGTGGCTCACACCTG | 55833 |
rs547979136 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027023 | CCTTTCAGATACCCA[C/T]ATGTTCTATACTGGT | 55833 |
rs548006745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046542 | CCAGCTACTCGGGAG[A/G]CTGAGCCAGGAGAAT | 55833 |
rs548045566 | in-del | -/GCCCG | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015619 | GGCATGAGCCACTGC[-/GCCCG]GCCTCAAGTGGATCT | 55833 |
rs548052759 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975427 | ACAGAGTGAGGCTCT[A/C]TCTTTAAAAAAAAAA | 55833 |
rs548063871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946710 | GTGTCAACAGAATTT[A/C]ATTTAAAAAAAAACA | 55833 |
rs548064351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982519 | AAGTGCCCATTTTGT[C/T]GCCCAGATAGTTTAA | 55833 |
rs548081777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008405 | GTTCCCTTTGAACCA[C/G]GATGGTGTGTGGAAG | 55833 |
rs548090418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995573 | ATTTAATTTAATTTA[A/G]AATTAAATTATTTAA | 55833 |
rs548124789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027230 | TCACACCTGTAATCC[C/T]GGCACTTTGGGAGGC | 55833 |
rs548124982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968701 | ATACAATACACATAA[C/T]ATGAAATCTATCCTT | 55833 |
rs548145097 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980162 | CTAATAATTCCGCTT[C/T]AATCCAAATCCTGAC | 55833 |
rs548178027 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980842 | GTCCCAGCTACTAGG[A/G]ACGCTGAGGTGGGAA | 55833 |
rs548233416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937445 | AACCCCACCTATACT[A/G]AAACTACAAAAATTA | 55833 |
rs548237513 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008343 | AAAAAAAAAGTGGGA[A/C]ACAGAAAATGAGTAA | 55833 |
rs548250243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038838 | CGTCTAGGAAGTGAG[A/G]AGCGTCTCTGCCCGG | 55833 |
rs548261239 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995002 | GTGTTCATCTTTGTA[C/T]CCTCTTTTAGGTGAG | 55833 |
rs548262129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002680 | CCGCCCAGCCTTAAC[A/G]TCTTTTTTTTAAGCT | 55833 |
rs548284498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002221 | TGCCTCCCAAAGAGC[G/T]GGAATTATAGGCATG | 55833 |
rs548302201 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039562 | CTTACCCCCAACCCC[A/G]TGCTCTCTGAAACAT | 55833 |
rs548437522 | snp | A/T | 1.83998e-05 | 0.00303308 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944684 | CATAATGGCTTCACA[A/T]TGTTCTTCAATAGAA | 55833 |
rs548446026 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934466 | AAAAACAAACATAAG[C/G/T]AATGAAAGGGTCAAC | 55833 |
rs548447115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023093 | TAGCCAGGCATGGTG[A/G]CACGCGCCTGTAGTC | 55833 |
rs548552628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028722 | AACCAGGACTCTTCA[A/C]CCTGGAATCTCTTGA | 55833 |
rs548568011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992276 | TCCTGTAATCCCAGC[C/T]ACTCGGGAGGCTGAG | 55833 |
rs548574566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986411 | AAAGCTCAAATGATC[A/G]TAGCCTTTTTTAGCA | 55833 |
rs548578051 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019616 | GTTGCACGACAATGT[A/C]AATGTACTTAATGTC | 55833 |
rs548603988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022102 | ATTCAAAAATTAGCC[A/G]GGCATGGTGGCGCAC | 55833 |
rs548620118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927681 | AGGTCAGTGGAACAC[A/G]CAGCGCACTCGGCGG | 55833 |
rs548626686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975334 | CTACCTGGGAGGCTG[A/G]GGCAGGAGAAATGCT | 55833 |
rs548642824 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016987 | CCACATACCCTAAAA[C/T]TTCAAGTATAATAAT | 55833 |
rs548646218 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043799 | GAGCCAGGCTCCAAC[-/T]TTTTTTTTTTTTAAA | 55833 |
rs548647980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027605 | GCTCACGCCTGTAAT[C/T]CCAGCACTCTGGGAG | 55833 |
rs548680375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940992 | TGTAGTGTCATCCAT[A/G]TTATTTTAATTTCCT | 55833 |
rs548683295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980487 | ACCTCGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 55833 |
rs548708195 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933603 | CACAGACGGGAGGGC[A/G]GAGGGAGGGCCTGTT | 55833 |
rs548712336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024282 | GGGAGGAAGAGGTTG[C/T]GGTGAGCCAAAATTG | 55833 |
rs548716607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030335 | GCACCTGTAGTCCCA[C/G]CTACTTGGGAGGCTG | 55833 |
rs548723846 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036073 | ATACAACATTTAAAG[G/T]GTTTTAACAATTTAA | 55833 |
rs548735531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021458 | ATTTTGTTGGTTTGG[G/T]TTTATCATTTTGGTT | 55833 |
rs548784115 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928066 | AGAGCCTGGCCTGGC[A/G]CTTGGGCCCAAGTCT | 55833 |
rs548787428 | in-del | -/C | 0.00303612 | 0.0388438 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932649 | AGACAAAACAGAGCG[-/C]CGTATGTCCACCTGA | 55833 |
rs548833447 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34048986 | ACGTCGCTCGTGCGC[A/G]GCTTCAGAGTCAGCC | 55833 |
rs548844333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980790 | GCAAAACCCTCTCTC[C/T]ACAAAAATTAGCTGG | 55833 |
rs548863613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971464 | CAAATTCCTTGTCAT[C/G]ATGAGATTTGTATGT | 55833 |
rs548890665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015232 | TTGCACCAGGTACTG[C/T]GCTTAGCACTTATCT | 55833 |
rs548893650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925109 | GGGAGGTCTGACCTG[A/C]CCCTCACTCACCATC | 55833 |
rs548897148 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922335 | ATTTACAAATACATA[A/C]ATAAATACATTACAT | 55833 |
rs548920788 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943820 | GCCTGTAATCCCAGG[A/T]CTTTGGGAGGCCAAG | 55833 |
rs548932634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990616 | CCTTTCTAGAAGGTT[A/G]CTTAGAAATAGTACC | 55833 |
rs549009718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982888 | TTTTTTTGTTTTTTT[G/T]TTTTTGTTTTTGAGA | 55833 |
rs549062680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009884 | GGGATCTCTGCTCAT[C/T]GCAACTTCCGCCTCC | 55833 |
rs549081581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023600 | TATAAATAATGACCC[A/G]GTTGCATGGCTAAAC | 55833 |
rs549113088 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946249 | ATTAAGGAAATTAAC[-/A]TCTTTTTGTCTATGA | 55833 |
rs549149082 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044913 | CCTAGTCTTAAATAA[A/G]ACACCTACTCTACTC | 55833 |
rs549189098 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965647 | ATTGAATTGCCTCAT[A/C]ATCTTTGACAAAAAA | 55833 |
rs549197555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003673 | TGCCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55833 |
rs549199514 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010607 | AGAGCAAAAAGGTAA[C/T]AGAACATATGGATAT | 55833 |
rs549248523 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961571 | TCTTATATAAGTAGA[A/G]GGCCATTGTTTACAG | 55833 |
rs549268022 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018900 | AAATAAAAAATAAAT[A/T]AATTAATTAAAAAGC | 55833 |
rs549295086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004872 | CTTTGGGAGGCTGAG[G/T]CAGGAGGAGACCAGC | 55833 |
rs549298461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973807 | TCAGAGAAAAACACA[A/G]AGCAAAAGCTTGACA | 55833 |
rs549311647 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001887 | TTTACAAGTCAAACA[C/T]AAGAAAAATTGAAAA | 55833 |
rs549318060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041548 | CTAAGAATACAAAAA[G/T]TAGCTGAGCATGGTG | 55833 |
rs549363244 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971098 | GTGAGCCACCGCGCC[A/C]AGCTAAATTATGTTT | 55833 |
rs549374959 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968251 | TGTAAACAGGAAGCT[G/T]GATGCAAGTCCTTCC | 55833 |
rs549379263 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040981 | AAACCAAAAATTCCA[A/C]TCTCAGTTATGTAGT | 55833 |
rs549403339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976127 | TATTACTGTGACTTA[C/T]AAGAATGTTAAGAAA | 55833 |
rs549416583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926511 | CTGAGAGGTTCCTCA[A/G]GCAGAGGATCCTAAG | 55833 |
rs549434411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932934 | CCTTGACAATCCCAT[C/T]CAATCTGTGAACGAG | 55833 |
rs549436264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940968 | CCTGCAGTATCTCCA[A/G]GGTATGCCTGTAGTG | 55833 |
rs549445210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041737 | AAAAAAGAAATCTAC[A/G]TGGGGGCTGGGTGCA | 55833 |
rs549473096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940222 | CTAGAAAGGCTTCTT[C/T]CTAAACTGGAAGCAT | 55833 |
rs549504141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948219 | TGCAAGTATTGTATA[A/G]CAAAGGAAGACTGAT | 55833 |
rs549576247 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012305 | GGAGGTCAAGGCAGG[C/T]GGATCACCTAAGGTC | 55833 |
rs549596701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955474 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 55833 |
rs549602898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047464 | TGTAGGATACGGGAG[A/C]GCTTAGGTATCATGT | 55833 |
rs549639913 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024896 | GGCTAAGGCAGGAGA[A/T]TCACTTGAACCCGAG | 55833 |
rs549660350 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998278 | TGATGAACATCTGTC[A/G]TCATAGCTACTCAGG | 55833 |
rs549669883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977486 | TCCCTGCATTGTTAT[C/T]TGGAATGAACAGATT | 55833 |
rs549670871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996665 | ATTTAATTCAAGCAC[A/G]CAGGATTCCTAAACT | 55833 |
rs549672332 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024130 | TTGGGAGGCCGAGCC[A/G]GCTGGATCACCTGAG | 55833 |
rs549673990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024193 | ACTAAAAATACAAAA[C/T]TAGCCGGGCGTGGGG | 55833 |
rs549709213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955762 | AACCCGAGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 55833 |
rs549732723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022294 | TAATACTCTGCAATT[C/T]CATCTTAAGTATCTA | 55833 |
rs549746360 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944176 | TAAGGATCTGTGGCT[C/T]TCAGCACAAACCCAT | 55833 |
rs549765592 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921543 | CAGCCATTGTGATTT[A/G]GGCCAAGAGGGTCCA | 55833 |
rs549812911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988319 | AATATATGAGACAGC[A/G]AGAGTCTCAGGGTGA | 55833 |
rs549817040 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047271 | GGAGTATGCTGGCAG[C/G]AAGCAAAAGGGCAGT | 55833 |
rs549850517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927636 | CAAGGAAGAATTCAT[C/T]CCCATCAGGGGTGGG | 55833 |
rs549870675 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028648 | GGCTCTTAAAGTGCT[A/G]GGATTACAGACACGA | 55833 |
rs549878490 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045237 | AGTAGTCCCAGGTAC[A/T]CGGGAGGCTGAGGCA | 55833 |
rs549887784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029480 | GTTGCAATGAGCCAA[C/G]ATTATGCCACGGCAC | 55833 |
rs549888287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989509 | CCCGGCACATGCACG[C/T]ATCTTTCAAACCTAA | 55833 |
rs549950538 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024673 | CAGACAAATTTTCCC[A/G]TATTAATTTTACATA | 55833 |
rs550007494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022926 | TTTATTCTCAGTGAC[C/T]CCATTTATGAAAATA | 55833 |
rs550038638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924440 | GTAAATGGTGCCCCT[C/T]GGAAGAGTGTGCAAC | 55833 |
rs550052746 | in-del | -/GGCCGAATGA | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927200 | TCAAAGAAGGGCAGT[-/GGCCGAATGA]GGCCGAATGAGGCAG | 55833 |
rs550069518 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036003 | GTAAGACCCTGTCTC[A/C]AACAAAATAGAACAA | 55833 |
rs550070721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978258 | TTAAACGTAAGCTGG[A/G]TCTGGTGGCTCATGT | 55833 |
rs550093361 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010740 | TGGGGTGGTAGATGT[C/G]TTAAACAGGAGCTAC | 55833 |
rs550102822 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021031 | TATTCCACTATTTGT[-/A]AAATCTTATACATTT | 55833 |
rs550107545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975500 | CATTGTGCACTGCTG[C/G]TAAAAACGTAAAATG | 55833 |
rs550161296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003630 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTTAAATG | 55833 |
rs550278375 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007383 | CACCATTAGTCCCAG[A/C]TACCCGAGAGGCTGA | 55833 |
rs550283925 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977071 | TGAGACAGAGTCTCA[C/T]CCTGTAGCCCAGGCT | 55833 |
rs550287812 | in-del | -/TCTC | 0.000441269 | 0.0148472 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943371 | TTTTCCACCAGTTGA[-/TCTC]TCTTAGGGTCTATTT | 55833 |
rs550294332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925644 | GGGGAGAAGCCGCTC[C/T]GCTCCCAGGCTAGGC | 55833 |
rs550299868 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969628 | TCCCATCACTTTGGG[A/G]GGCCAAGGTGAGTGG | 55833 |
rs550349463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046732 | TACTTTCTACACATA[G/T]TTTATACTTAAGAGG | 55833 |
rs550352390 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969654 | AGTGGATCATTTGAG[C/G]TCAGGAGTTCAAGAC | 55833 |
rs550376164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009000 | AAAGTTAACATTTAG[G/T]ATAGCGGGGTGAATA | 55833 |
rs550391109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013745 | AGCCAGGCATGGTGA[C/T]ACATGCCTGCAATCC | 55833 |
rs550392721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006157 | AGAATCGCTTGAACC[C/T]GGGAGGCCAGAGGTT | 55833 |
rs550393599 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951556 | TTTACCACATTGGCC[A/G]GGCTGGTCTCAAACT | 55833 |
rs550416925 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002062 | CCCAGGCTCAAGCAC[C/T]CCTCTGACCTCAGCC | 55833 |
rs550438314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968763 | ATTCACAATTTGTGC[A/C]ATCATCACCTCTAAT | 55833 |
rs550449130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923126 | TGCCCTGCCTGAGAG[A/G]GGATCAGGCAGGAGC | 55833 |
rs550468373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954633 | CTCATTCCTGACACA[C/T]GGCAAAGTTCCTAGC | 55833 |
rs550477251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006897 | TGACAGTGACTACTG[A/G]ACATATTATTTACTA | 55833 |
rs550513327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979594 | AAAATAAAAATAAAA[A/T]ATAACTGGCCAGGTG | 55833 |
rs550515409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026170 | AACATACTGAGAAGA[A/G]GGAAGATTTCAACAG | 55833 |
rs550593979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962553 | GAGGAGGCTGAGGCA[G/T]GAGAATCGTTTGAAC | 55833 |
rs550609774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923545 | TGGTCAGGTACCCCT[A/G]CCAGAGCCTAAGGCA | 55833 |
rs550618807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000129 | TATTTATTTAATTTT[A/T]TAAAGGTAGGGTCTC | 55833 |
rs550674659 | snp | A/T | 1.64852e-05 | 0.00287094 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973162 | GTAAATAATTATAAA[A/T]ATAGGATGGCTATCA | 55833 |
rs550687796 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34048902 | TGCCTCTTACAAAGC[A/C/G]GCGGCGGCGGCACAG | 55833 |
rs550723914 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940704 | GGACTCACTGAGCCC[A/G]GGAGGTCAAGGCTGC | 55833 |
rs550771494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990862 | GGGTGCTCTCGAACT[C/T]CTGACCTCAGGTGAT | 55833 |
rs550807085 | in-del | -/TAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962676 | AAATAAATAAATAAA[-/TAAT]TAAATAATTAAAAAA | 55833 |
rs550813810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004831 | TTTAAGGCTGGGCAC[A/G]GTGACTCACGCCTAT | 55833 |
rs550827271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965438 | TTCAGAAGAATTTTA[C/T]AATTTTTGATAAAAT | 55833 |
rs550832553 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042472 | GATAGTGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 55833 |
rs550877258 | snp | A/G | 0.000395302 | 0.0140533 | missense | UBAP2 | GRCh38.p7 | 9:33941750 | AAGACATTGCTACTG[A/G]ACTAGCAGAATTCAG | 55833 |
rs550888944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044738 | AAGTGTGTTGGCAGG[C/T]GCCTGTAACCCCAGC | 55833 |
rs550929025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024851 | TAGCTGGGTGTGGTG[C/G]CGTGAGCCTGTAATC | 55833 |
rs550963708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991287 | GCCTGGGTGACAGAG[A/C]GAGACTCTGTATCAA | 55833 |
rs550971075 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922221 | GCAGATGGGGTGGGG[A/G]TGCTTATTTTGCTAC | 55833 |
rs550987482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971421 | ATTACCTTATATAGC[C/T]TCTTTCTTAGCTTGC | 55833 |
rs551025428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011242 | CTGTTTCACCCATAC[A/G]TTTCTAACTATAAAG | 55833 |
rs551033227 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036929 | TCCAGCAATTCTCCC[A/G]CCTCAGCCTCCCAAG | 55833 |
rs551065830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025512 | AAAGATGTGATAGAT[G/T]TTAACACAGGTAAAG | 55833 |
rs551075539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934546 | TTCCATATATAAACC[C/T]TGTTCATAGATAAAC | 55833 |
rs551079272 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049498 | TGCCTGCTGGGAGGT[A/G]TAGTCCTGGCGGGGG | 55833 |
rs551084034 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016452 | AGGTACCTGGAAAAG[C/G]TTAGCATTAAAGAGT | 55833 |
rs551090000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984199 | ATGAGCCACCACACC[C/T]GGCCTGAATCCCTGG | 55833 |
rs551146233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037325 | TTTTTGGTAGAGGTA[A/G]GGTTTCACCATGTTG | 55833 |
rs551146782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950426 | TACTTTGCCTTCCCT[A/C]AAGTAAGTTGAAACA | 55833 |
rs551189232 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019721 | CACACACACACACAC[A/G]CACGCACAGAAAAAC | 55833 |
rs551196674 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017626 | CTGTAAATAATAAAT[C/G]TTAAAGAAACAATTG | 55833 |
rs551211143 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039350 | CACCTCATCTGGGAG[A/G]TGTACCCAACTGCTC | 55833 |
rs551217203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958325 | CTTACAAATTAAATC[A/G]ATTTACGAAAAAGAG | 55833 |
rs551262294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942393 | AAACTTAAACAAATA[C/T]CAGGTTTTGCCTCTG | 55833 |
rs551265217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935110 | TACAGAAAAGAAGCA[A/G]TTAACGGATTTACCT | 55833 |
rs551273408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031394 | GCTTACTGCAACCTC[C/T]ACTCCCAGGTTCAAG | 55833 |
rs551297536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923507 | CAGATGAGGTATTAG[G/T]GTAGGAAGAGGCAAG | 55833 |
rs551321540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984751 | AAGGTACACAAAAAA[C/T]GCTCATCACTAAACA | 55833 |
rs551336511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030785 | TTTTTAAAAAATTAG[C/G]TGGGCATAGTGGCAG | 55833 |
rs551400640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005476 | TGATAAAAGAATAAC[A/G]TATCTCTAAGTTTTT | 55833 |
rs551403852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977440 | TGGTAGTAACGCTAC[C/T]AGTAACATTGGTTTC | 55833 |
rs551405691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969986 | CCAGGCTAAAGTGCA[A/G]TGGCACGATCTCAGC | 55833 |
rs551417232 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989782 | TATTAGGCCTTAAAT[C/G]TACTTATTAATTCAA | 55833 |
rs551417645 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928710 | GGGTCCTATGAAGAA[C/G]TTCAAGCTCCGAGCA | 55833 |
rs551545469 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028810 | CCTACAAAAAGGAAA[A/C]AAAAAAGCAAAAAAG | 55833 |
rs551583391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004415 | CCTTAGCCCGAGGAG[A/G]TCAAGGTTGCAGTGA | 55833 |
rs551593985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010717 | GAAAAGGAGTACAGG[C/T]GGCGGCTTGGGGTGG | 55833 |
rs551595072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997546 | CAAGCAGCAAAAGTT[C/T]TGCATACTCTATAGC | 55833 |
rs551668014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013101 | ACAGTTGCCGTTAGC[C/T]GAGATCAAGCCACTG | 55833 |
rs551678382 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997235 | TAGCAAGAGATACTT[C/G]TTACTTAGCATTTTC | 55833 |
rs551681476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998165 | CCAGCACTCTGGGAG[A/G]CCAAGGCAGATTGCT | 55833 |
rs551704367 | in-del | -/TA | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937189 | TCAAGAACTAATGTC[-/TA]AAACCAGGATGGAAA | 55833 |
rs551710598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967017 | AAATATATTAAAGTG[C/G]TATATCCCTCTATTT | 55833 |
rs551718365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965156 | CGTGTTAAAACAGAA[A/C]ATTTACCATTTCTGA | 55833 |
rs551732997 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966224 | AGGCTGAGGTGGGCA[G/T]ATCACTTGAGGTCAA | 55833 |
rs551794798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974524 | AAACAAACAAAAAAA[C/T]ACCACGGTACCAACA | 55833 |
rs551796898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966535 | TGTGCTGAAGCTATC[A/G]ATCAATTTGGAGAGA | 55833 |
rs551825221 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938971 | GAAGAGAAAAAGGAA[A/G]GGAGGATGATCCATC | 55833 |
rs551828326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036568 | TACACACATTTAAAC[C/T]GTGTGTGTCTGCTCA | 55833 |
rs551850148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011189 | GCTGTAGGGGGCAGT[C/G]TGGGGCTTATATATG | 55833 |
rs551875258 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042783 | TTACTTTTTTTTTTT[A/T]ATTTTACATATGGGG | 55833 |
rs551909817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925044 | GTATGGCAGATACAA[C/T]AAAGTGTGGAGACAG | 55833 |
rs551933464 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921311 | CCTGTTCATACTCTC[C/T]CTTAAGGCCTAGAAC | 55833 |
rs551987823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004733 | AGCTTGCAGTGAGCC[A/G]AGATAGCGCCACTGC | 55833 |
rs552009793 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953190 | TAGATATTTTTATAT[A/T]TAGAAAGTAATTATA | 55833 |
rs552011072 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022698 | CCAGCCTCAGCCTCC[A/G]AAGTGCTGGGATTAC | 55833 |
rs552030938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037156 | ACCATGCCTGGCTAA[C/T]TTTTTGTATTTTTAA | 55833 |
rs552039436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987592 | TCAGCCTGGGTGAAA[C/G]AGTGAGACCTTGTCT | 55833 |
rs552066686 | snp | A/G | 0.000461429 | 0.0151823 | missense | UBAP2 | GRCh38.p7 | 9:33941668 | ATGGTTCCTGGAGCT[A/G]ACTCTGATGAACTCA | 55833 |
rs552072534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044652 | GGTGGATCACCTGAG[A/G]TCAGGAGTTCCAAGA | 55833 |
rs552074653 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020736 | TTGATCTCTGCTCAC[A/C]GCAAGCTCTGCTTCC | 55833 |
rs552077356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953648 | ACACAAAAGAACATA[C/T]CAAGCCACAGAGACT | 55833 |
rs552106526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044612 | GCTCACGCAAGTAAT[C/G]CCAGCACTTTGGGAG | 55833 |
rs552126265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002084 | ACCTCAGCCTCCTGA[A/G]TAGCAACCATGGCAG | 55833 |
rs552142550 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029080 | ATGATCATGTCACCG[C/T]ACTCCAGACTGGGCA | 55833 |
rs552147296 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957954 | GGTGTGTGGGAAGGG[A/C/T]TTTTTTTTCTTTTTT | 55833 |
rs552159578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956489 | ATGCGCCACCACACC[A/G]AGCTAATTTTTGTAT | 55833 |
rs552165278 | in-del | -/AT | 0.489608 | 0.0713316 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981064 | GGGCTTATTTACTTC[-/AT]ATATATATATATATA | 55833 |
rs552200972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001547 | GGCAGCTGGCCTGCA[A/G]TATAATCCCTGGGCA | 55833 |
rs552208881 | snp | C/T | 0.00187074 | 0.0305265 | missense | UBAP2 | GRCh38.p7 | 9:33927077 | AAGTTTGGGGGTGCT[C/T]TGCCTGTATAGAGGG | 55833 |
rs552222794 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981239 | TGGATATATATATAT[A/T]TTCTGGATATATATA | 55833 |
rs552255718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943248 | TGGTTGCTAAGGGGC[A/G]GGGCAATGAAGAAAC | 55833 |
rs552268171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959023 | GCATGGTGGCGTGCA[C/T]CTATAATTCCAGCTA | 55833 |
rs552282797 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976757 | ATCCTAGCACTTTGG[A/G]AGGCTGAGGCAGGTG | 55833 |
rs552294487 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038492 | GTTTCGCTGTGTTGG[A/C]CGGGCTGGTCTCCAG | 55833 |
rs552327692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045379 | AAAATAAAAATTAAA[A/G]AAAAAATTTTTTTTT | 55833 |
rs552354198 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039434 | AATGTGGGGAAAAGA[C/G/T]AGAGAAATCAGATTG | 55833 |
rs552372259 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939015 | GGACACAAATATTTT[C/T]CTAAATGTTTAGTTG | 55833 |
rs552379539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985533 | ACATGAATGGACTTG[C/G]AAGACATTGTGTTAA | 55833 |
rs552392840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945010 | TCACTCATGCCTATA[A/G]TGCCAGCACTTTGGG | 55833 |
rs552410458 | in-del | -/TT/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958706 | CCACTGTGCCCGGCC[-/TT/TTT]TTTTTTTTTTTTTTT | 55833 |
rs552415601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039013 | TCTGCCCGGCCGACC[C/T]GTCTGAGAAGTGAGG | 55833 |
rs552431073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974023 | CCAGCCTGGGCAACA[C/T]AGGGAGACTCCCTCT | 55833 |
rs552471742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938206 | ATCATGTTGTCCAGT[C/T]TGGTTGTGAACTCCT | 55833 |
rs552477588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034365 | TTTTATTTTACTGAC[A/G]TCCTTATTACTTAAT | 55833 |
rs552483327 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033913 | GCTAATTTTTGCATT[A/T]TTAGTAGAGACGGGG | 55833 |
rs552504386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945591 | CATACTTGCTCCACA[A/G]AGGCAAACACTGTAC | 55833 |
rs552554081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930679 | GAGGCGGGTGGATTA[C/G]GAGGTCAGGAGTTTG | 55833 |
rs552571655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957666 | TGTTTTCAATGTGGG[A/G]ACTCGGCTTTGAAAG | 55833 |
rs552600926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027582 | AAAAAAATAGGCCAG[A/G]CACGGTGGCTCACGC | 55833 |
rs552661244 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999325 | ATTTTTAAAAAGATT[A/T]AAAAAAAAAAAGGCT | 55833 |
rs552682920 | in-del | -/T | 0.221737 | 0.248397 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002378 | CCACTGCATAGGTGC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs552703555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980318 | GGTCACTACGAGCTC[C/T]GTCTCCCAGGTTCAC | 55833 |
rs552707564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026995 | CTAGATCAGATCTCA[A/C]CTAGCTTCTCAGCCT | 55833 |
rs552729694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000637 | ACAGTTTACAAAAAG[A/T]TCTTAGAGGAAGAAA | 55833 |
rs552734111 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019478 | AAGTCAAATTCATAG[A/G]AACAAGTAGAATGGT | 55833 |
rs552739005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986372 | TAGAAGTGAGGACTA[A/G]AGCAAAAAGACTACA | 55833 |
rs552745663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991966 | TCATATAGCAAATGA[C/T]ACCCTGGCCAGGCAC | 55833 |
rs552759673 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021650 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGGCTCGC | 55833 |
rs552816095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014919 | CTATCAGAGTAAGTG[C/T]ATTTAGGATCAAGCA | 55833 |
rs552822309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929586 | AAAATACACAGATCT[A/G]TGTAAAAAAAAATCA | 55833 |
rs552826188 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020166 | AAAAAAAAAAAAAAA[A/C]AAAAACTAAGAGATA | 55833 |
rs552881383 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930018 | TCAGAAAAATAATAA[C/G]AAATAAATAAATAAA | 55833 |
rs552882493 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956663 | GATTGAAAGGCCTAC[A/G]AGAATGACTTCAAAT | 55833 |
rs552893241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021348 | TTCTCACAGCCTCAA[G/T]ACACTGGTTTAAAAC | 55833 |
rs552905517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020610 | AGATTACAGGCGTGT[A/G]CCACTGAGCCGGCCC | 55833 |
rs552947558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949925 | AAAAACAATGTTACT[A/C]CTGCCCCATCTGTCC | 55833 |
rs552955952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936855 | TCCAGCTACTCAGAA[C/T]GCTGGAACAGGAGAA | 55833 |
rs552982510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986452 | TTTAAAATAAGGTTT[A/T]AAAAACCCTATTGCA | 55833 |
rs552986320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949294 | ACATGACAAAGATAT[A/G]CTTGACCAACAAAAA | 55833 |
rs552991233 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005985 | CCTATAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 55833 |
rs552999575 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050609 | GGCTCACACCTGTAA[G/T]CTCAGCACTTTGGGA | 55833 |
rs553011824 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050000 | CTATCTTGTCACCCC[A/G]TAGATCGCCAGGGCT | 55833 |
rs553099410 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036329 | TCCATGTTGGTCAGG[A/C]TGGTCTCAAACTCCC | 55833 |
rs553103640 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931408 | TACATGGTCTGGAGG[-/T]TTTTTTTTTGAGGAG | 55833 |
rs553105594 | in-del | -/A | 0.452129 | 0.147119 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945142 | TTCATCCAAAAATTA[-/A]AAAAAAAAAAAACTT | 55833 |
rs553109279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990181 | GCCCAATAGTTTCCA[C/T]TTACTTATTCATAAT | 55833 |
rs553116305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950932 | ACACAAACACACACA[C/G]TGCCCAAATCCCAAT | 55833 |
rs553137542 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015166 | ACTTGCATATTGCCT[A/G]TGAAAAAGGGTTTGC | 55833 |
rs553138981 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000252 | CCCATGTAGCTTGGA[C/T]TACAGGTGCGCACCA | 55833 |
rs553149519 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038275 | CCAACACAGTGAAAC[C/T]CTGTCTCTATTAAAA | 55833 |
rs553149981 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967457 | GAAAGTTTACAGATA[G/T]TCCTTATCTGATTAA | 55833 |
rs553193123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934109 | CGGCCAACGTAAGGC[A/C]GATTGGGGTTGATGC | 55833 |
rs553193610 | in-del | -/AAGA | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939939 | AGGAGAAGGAAGAAG[-/AAGA]AAGAGGGAAGGAAGG | 55833 |
rs553231444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972767 | AAATAAGCATTACAT[C/T]TACTTAGCATTCAAA | 55833 |
rs553238678 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978658 | CTGGCGGGTGCCTAT[-/A]AGTCCCAACTATTCG | 55833 |
rs553258770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971878 | CACTGTAAAAGACAT[C/T]ACCTCTCCTTCCCCT | 55833 |
rs553264371 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032251 | CAGCTGCAGGAATCC[C/G]CATCTATCCTCTCTT | 55833 |
rs553273068 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962831 | AAAATACAAAGAATT[A/C]GTCAGGAGTGGTGCC | 55833 |
rs553327020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036760 | GCAGTAATGTAAACT[C/T]AGCATTCACAGAAAT | 55833 |
rs553339194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042636 | TATTTTAAAACAACA[A/C]CACAAAGGAATAGTA | 55833 |
rs553367360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964018 | TATTCTCATTCTCAC[A/G]CCCATGTTTACCAAG | 55833 |
rs553378647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945264 | AACACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 55833 |
rs553396441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934819 | CCACTACCACTGCTA[A/G]AGTCAAAAGTTCCTC | 55833 |
rs553402603 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942267 | CAGTGAACCAAGATC[A/C/G]CGCCACTGCACTCCA | 55833 |
rs553443069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034081 | CCTAAAATAATAGTT[A/C]TCATTATTCACATCT | 55833 |
rs553443716 | snp | A/T | 0.00516055 | 0.0505336 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941876 | CACTGAAAAGAGTCA[A/T]AAATATTCAACATAA | 55833 |
rs553519279 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984822 | TACCCCAGTTAGAAC[A/G]GCTATTATCAAAAAG | 55833 |
rs553538629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030415 | GATCGCGCCACTGCA[A/C]TCCAGCCTGGGCGAC | 55833 |
rs553552251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975614 | CCATCCTGGCTAACA[C/T]GGTGAAACCTCATCT | 55833 |
rs553579643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928429 | CACAGGAAGCCCAGC[A/G]TAAGTCTCAATCTTT | 55833 |
rs553596565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938594 | CTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGGC | 55833 |
rs553617368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012774 | TAAAATCTGGGGAAT[C/G]TGAAAAAAGGGTATT | 55833 |
rs553624687 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024962 | ACACTCCAATCGGGG[C/T]GACAGAACAAGACTC | 55833 |
rs553630781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969071 | TGCTTATACATTCAT[A/C]CATTGATAAACATTT | 55833 |
rs553676296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019334 | CTTGAACCCAAGAGG[C/T]GGAGGTTGCAGTGAG | 55833 |
rs553730715 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029254 | TACATAGGGCCAGGC[A/G]TAGTGGCTCAGACCT | 55833 |
rs553742510 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986318 | ACAGTAGAGTAAGAT[A/G]ACTACTTAACAATTA | 55833 |
rs553758258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027744 | CGGGTACCTGTAGCC[C/T]CAGCTACTCAGGAGA | 55833 |
rs553783601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016587 | TTAGGAAGGAGTCTC[A/G]CTTTGTCACCCAGGC | 55833 |
rs553785491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027349 | AGCCAGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 55833 |
rs553817579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995075 | AGAAACATAAACACA[C/G]GTCAGGTGTGGTGGC | 55833 |
rs553841731 | snp | A/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931098 | ACAGTTGACCCCTGA[A/G]CAACACAGGCTTGAA | 55833 |
rs553856994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930125 | AAAACTAGACTGATG[G/T]GCCATTTTTCTGCTA | 55833 |
rs553859911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981274 | TTCTGGATATATATA[C/T]ATATTCTGGATATAT | 55833 |
rs553879176 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022456 | TTTTTTTTTTTTTTT[A/G]AGACACAGTCTGGCT | 55833 |
rs553896594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015789 | TCCTCCCACCTCAGC[C/T]GCCCAAGTACCTGGG | 55833 |
rs553937256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045522 | GGGACTACAGGCACG[C/T]GCCACCACACCAGGC | 55833 |
rs553949368 | snp | A/C | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045118 | TTTGGGAGGCCGAGG[A/C]GGGCGGATCACGAGG | 55833 |
rs553974888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023118 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55833 |
rs553993630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925947 | GGCAGGGCAAGGAGC[A/G]GGCCTATTCCCCTCT | 55833 |
rs554047928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007888 | CCTCATGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 55833 |
rs554122774 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930724 | AACATAGTGAAATCC[C/T]GTCTCTACTAAAAAT | 55833 |
rs554142943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952979 | GGCACAAGTGACCCT[C/T]CAACCTCAGCCTCCC | 55833 |
rs554176945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974222 | CTGTAACAAAACACA[C/T]ATTGGCTAGGCACGG | 55833 |
rs554207635 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936084 | ACATCCCCAGGTTCA[C/G]GTGATCCTCCCCCTT | 55833 |
rs554213658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980521 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 55833 |
rs554215114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966659 | CATAATATTAACATA[C/T]AAATCTTGCATATAC | 55833 |
rs554237012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987158 | GCTCACACCTATAAT[C/T]CCAGCACTTTGGGAG | 55833 |
rs554263401 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039125 | GCGTCTCCGCCCGGC[A/T]GCCGGCCCGTCTGGG | 55833 |
rs554314761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981795 | TAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGGTG | 55833 |
rs554319101 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982588 | TCACCGGTATATATA[C/G]TGATGAGAAAATTAT | 55833 |
rs554320860 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003245 | CATGTTGGTCAGGCT[A/G]GTCTTGAACGTCTGA | 55833 |
rs554347615 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981118 | GATATATATATATAT[A/T]TATATATATATATAT | 55833 |
rs554377722 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945155 | TTAAAAAAAAAAAAA[A/C]TTATTAAGTTTTTGG | 55833 |
rs554382434 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001112 | AAGGGAAAAGCAAAG[A/G]GAGAGATGGGTTTTT | 55833 |
rs554383081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958644 | AACTCCTGACCTCAG[A/G]TGATCCGCCCACCGC | 55833 |
rs554398253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993875 | AAGAGGTGTTCTTCA[C/T]GAAAAGTTCAGCTTT | 55833 |
rs554468062 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021837 | TGGGGTCTCAACTTG[A/T]TGGTCAGGCTGGTTT | 55833 |
rs554476938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039165 | GCAGCCTCCGCCCAG[C/T]CAGCCGCCCCTTCCG | 55833 |
rs554516181 | in-del | -/T | 0.158962 | 0.232835 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958707 | CCACTGTGCCCGGCC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs554521547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936135 | CTACAGGTGCATCCT[A/G]CCATGCCTAGCTAAT | 55833 |
rs554530741 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926564 | GACCATAAGAGGGGG[C/G]ACATGTAAAAGATTC | 55833 |
rs554549592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015441 | CTCCCTGCCTCAGCC[C/T]CCCGACTAACTGCCA | 55833 |
rs554558682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038707 | GCCCGGCCGCCACCC[C/T]GTCTGGGAAGTGAGG | 55833 |
rs554599933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032789 | ATTAGCTGGGCGTGG[C/T]TGCACGCACCTGTAA | 55833 |
rs554612564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022372 | AGCTATTCAGGAGGC[C/T]GAGGCAGGAAGATCA | 55833 |
rs554675588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979237 | AGTGAGACCCTGTCT[C/T]TAAAAAAAGAAACTA | 55833 |
rs554690049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025895 | TAACTGCTGTTTTTT[C/T]CAAGGACCTTTCTGA | 55833 |
rs554705816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021795 | CCTGCCACCACGCCC[A/G]ACTAATTTTTGTATT | 55833 |
rs554720281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975030 | CACATTAAAAGATAC[C/T]CAGTATTGCTGATCA | 55833 |
rs554738804 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950223 | GGCGCCCACCACCAC[A/G]CCCGGCTTTTTTGTT | 55833 |
rs554749251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020654 | TTAACAATACATGGA[A/C]CTCTGTTTCCTTTTT | 55833 |
rs554782221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931027 | GTAGATGAGAGACAG[A/C]AAAACTTTTCATTGT | 55833 |
rs554784780 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050892 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 55833 |
rs554801606 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025104 | AACTGTAAAAATGAC[C/T]GAGACATGGAAACTA | 55833 |
rs554860009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925683 | CTGGAAATACGGCCA[A/G]CCAGTGGAAAGGGCT | 55833 |
rs554863024 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047549 | GTGAAAAGTGAGGAA[A/T]GCAATAACTAGTCGC | 55833 |
rs554866906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958530 | CTCCTGCCTCAGTCT[C/G]CCAAGTAATTGGAAT | 55833 |
rs554880103 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924509 | AACCCTGCAGCTTCA[A/C]CAGGCAGAGCTGCTG | 55833 |
rs554893655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014923 | CAGAGTAAGTGTATT[G/T]AGGATCAAGCACTGA | 55833 |
rs554917991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926791 | GGATCTGGATTAGCT[A/G]TTACGGGAACAGATC | 55833 |
rs554957625 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050687 | CCAACACGGTGAAAC[C/T]CCGTCTCTGTTAAAA | 55833 |
rs554972279 | in-del | -/A | 0.00641533 | 0.0562717 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966903 | AATCTAATTTTTTTT[-/A]AAAAATCAGTGGGGA | 55833 |
rs554973269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979866 | AGTGAGACTCTGTCT[C/T]TAAATAAATAAATAA | 55833 |
rs554977453 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933263 | ACCCTACTCCCAGGG[A/G]ACCCAGTGCTCTGTG | 55833 |
rs554998158 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930592 | TTATGTAACAAGAGA[A/G]AAAGAATAAAAAGGG | 55833 |
rs555009773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985753 | TAGGCCGGGCTCGGT[G/T]GCTCATGCCTGTAAT | 55833 |
rs555042486 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012908 | ATAATCCGGGCAGTT[C/G/T]GGGAAGCTGAGGTGG | 55833 |
rs555083180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013383 | GGTGAAACCCCGTCT[C/T]TACCAAACATACAAA | 55833 |
rs555094126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955627 | TGAGGTTGGGAATTC[A/G]AGACCAGCCTGACCA | 55833 |
rs555124207 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047399 | GGAAACTATCATCTC[C/T]AGGGAGTGGAATACA | 55833 |
rs555130948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017396 | GGTTTACGAGCTTAG[C/T]AATTCTAAACAAAAA | 55833 |
rs555137008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048570 | TGGGGCTGGGTGGGG[A/C]CCAGCCGACCTGGAC | 55833 |
rs555143138 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032826 | CTAGTCCAGAGGCTG[A/G]GGCACGAGAATCACT | 55833 |
rs555143853 | in-del | -/TTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987700 | CATACTGATTTTTCT[-/TTC]TTCTTTGTGGACTTG | 55833 |
rs555147668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970261 | TTCACGTTCTCACCT[C/T]CCCTTGATGATCTCA | 55833 |
rs555149468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047948 | ATATCCAATAGAAGT[C/G]GTAGTAAATGACTGG | 55833 |
rs555173246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014066 | AGTGGCTCACACCTG[C/T]AATCCCAACACCTTG | 55833 |
rs555193065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965918 | GCCAGGTGTGGTGGC[A/G]GGTGCCTGTAGTCCC | 55833 |
rs555215682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045073 | TAAAAAAAGGCTGGG[C/T]GCCGTGGCTCACCCC | 55833 |
rs555221328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017347 | TTTTGCTGGTATCTG[C/T]TAAACCAATTCGACT | 55833 |
rs555313266 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008596 | GTAATAAAATCAAAA[G/T]GCAACAGAGATTGTG | 55833 |
rs555343360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042069 | CAAGCATGTAAGAGT[C/G]AAAGAATCAAGCATC | 55833 |
rs555364908 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024043 | GCAAGACTCTGTCTC[-/A]AAAAAAAAATAAAAA | 55833 |
rs555370258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997703 | GATCAGATTATTGAC[A/G]GACAGAACTAAAATT | 55833 |
rs555377566 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998529 | GTGTGCTTACAGAAA[C/T]GTCTGGTTCAATGTT | 55833 |
rs555400442 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955712 | ATGCCTGTAATCCCA[A/G]CTACCTGGGAGGCTT | 55833 |
rs555436254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002987 | ACCACAGTGCCCGGC[C/G]TATATCTTTCTTACT | 55833 |
rs555448446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002470 | GCAACCTCCATCTCC[A/C]AGGTTCAAGCGATTC | 55833 |
rs555491171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962635 | GGCAACAGAGCAAGA[C/G]TCTATCTCAAAAATA | 55833 |
rs555525536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968529 | CCATGTTGGTGGAAT[C/T]AAGGGCCATTATCAG | 55833 |
rs555577195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970905 | CCTCCTGGGTTCAAG[A/C]GATTCTCCTGTCTCA | 55833 |
rs555592781 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039930 | TTGGGAGGCCGAGGC[A/G]GGCGATCACCTGAGG | 55833 |
rs555606469 | snp | C/G | 1.67256e-05 | 0.0028918 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932613 | AGAGAGGCTGCTCTG[C/G]TGGCTGGAGAGCGAA | 55833 |
rs555672079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028985 | GCCACGCTTGGTGGC[A/G]CACACCTGGAATCCC | 55833 |
rs555680967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947463 | CCACGGAATGTAAAG[A/G]TTGATGAAATCATAG | 55833 |
rs555688674 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040558 | CACGACCAGCCCAGC[C/T]AACATAGCGATACAC | 55833 |
rs555694442 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945237 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 55833 |
rs555700505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996027 | CTCTTTCAAGTCATC[A/T]GATTCTACGACTTCA | 55833 |
rs555707921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004554 | TTGGGAGGCCAAGGC[C/G]GGTGGATCACGAGGT | 55833 |
rs555713757 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958891 | CAGTGGCTCATGCCT[A/G]TAATCCCAGACCTTT | 55833 |
rs555754264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034650 | GAGGCACAGGCGGGC[A/G]GATCAGGAGGTCAGG | 55833 |
rs555760337 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008137 | AGACTCGTCTCAAAA[-/AAC]AAAAATACACATACA | 55833 |
rs555783983 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042456 | ACACTTCAGCCCAGG[C/T]GATAGTGCAAGACTC | 55833 |
rs555786700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939584 | GTAACATGATGAAAC[A/C]CCATCTCTACAAAAA | 55833 |
rs555800258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039924 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGATCAC | 55833 |
rs555801677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964235 | GCTGAGTCCTGGACT[C/T]ATAACTCTCTTATCA | 55833 |
rs555817092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988769 | TGTTAACTATTAGAA[C/T]AAATTCTGCATTGAG | 55833 |
rs555836432 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020898 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 55833 |
rs555836707 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991184 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 55833 |
rs555838946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028922 | GAGGTGAGCAAACCT[A/G]GGCGGCGTGGCAAGT | 55833 |
rs555862961 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989412 | TTCATCGTGTTAGCC[A/T]TGATGGTCTCGATCT | 55833 |
rs555897567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970085 | CAGGCATATGATACT[A/G]TGCCCGGCTAACTTT | 55833 |
rs555897632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960961 | CCTTTTTGTGTACTA[C/T]GCGGGGAAAAAAGAT | 55833 |
rs555920301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960706 | AACTGCTTGAATCTG[A/G]GAGGCAGAGGTTGCA | 55833 |
rs555927398 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947690 | ATCAGCCAGGAGTGA[C/T]GGCATGTGCCTATAG | 55833 |
rs555964151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946401 | TTCTAGATTCACTAT[G/T]TATGTTTAACTATCT | 55833 |
rs555972299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976501 | CCTACAGAAACAGAA[A/G]GGCGATTACTGGTGC | 55833 |
rs555985181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969250 | AGTTGATTTGACTTG[A/T]TTTTTAAAAGTTAAA | 55833 |
rs555985744 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028208 | GAAAGGATGAGTGCT[A/G]GTGAACTCAAACACT | 55833 |
rs556019464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989242 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55833 |
rs556025209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023155 | CGCTTGAACCCAGGA[A/G]GCAGAGGTTGCAGTG | 55833 |
rs556033091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954715 | ATCCCAGTAAATTCA[A/C]TGAATCATAAATACA | 55833 |
rs556086064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982710 | GATTAAGAAAAACTA[C/T]GGTGATTTTACATGG | 55833 |
rs556114984 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042910 | GACTCCTCTCTACAA[A/C]AAGAAAAATTAGCTG | 55833 |
rs556139893 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955681 | AAAATACAAAATTAG[C/T]TGGGCGTGGGGGCGC | 55833 |
rs556146794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028457 | CAACACTGGCTCACT[A/G]CAACCTCTGCCTCTT | 55833 |
rs556154871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947235 | CAGTAAGTCATTTCA[C/T]AGAACAGAGGAATAT | 55833 |
rs556195860 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940092 | AAAGAAGAAAAAAAG[G/T]AGGAGGAGGAAGAAG | 55833 |
rs556206359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988718 | AAACCACATGGGAGG[C/T]GCTTATGAAACTACT | 55833 |
rs556244348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015350 | TTGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 55833 |
rs556266137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925303 | GCTGGGAACACACAG[A/G]GCTGCACAACTGAGG | 55833 |
rs556306901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927250 | GTGAAGGGGAGACAG[A/G]AAGCCCGGCCACCAC | 55833 |
rs556329961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974959 | GGGGTGCGGGGGGGC[A/G]GGCAATGGACTTGAA | 55833 |
rs556361366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017174 | TACAAAATAATGTAT[A/G]TACAAAATAGAAAAT | 55833 |
rs556401039 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021464 | TTGGTTTGGGTTTAT[C/T]ATTTTGGTTGTATTA | 55833 |
rs556475858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954025 | GATTCTCGTGCCTCA[A/G]CCTCCCGAGTAGCTG | 55833 |
rs556490028 | snp | C/G | 0.000197674 | 0.00993972 | missense | UBAP2 | GRCh38.p7 | 9:33924239 | CTAGGCTCCCATCTC[C/G]GCTGGCAAGCGCTGT | 55833 |
rs556492268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046322 | AAAAAAAAGAGGACT[C/G]GGAAATCAACAATTC | 55833 |
rs556500158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010080 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 55833 |
rs556509594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011948 | CCCAGAAAAAAATTG[G/T]AAATAATAATAAAGT | 55833 |
rs556555278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967634 | AAAGGCAAAGCACCA[C/T]AGGTAAAGCTGATCA | 55833 |
rs556576582 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023166 | AGGAGGCAGAGGTTG[A/C]AGTGAGCTGAGATCG | 55833 |
rs556586119 | in-del | -/C | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964741 | AGCAAGAAAAAAAAA[-/C]ATCAGTGGAGGTATT | 55833 |
rs556586294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946287 | TTTGAGTATTTTTTT[A/C]ATTGTTTGTCTGCCT | 55833 |
rs556613171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001970 | ATTTTTTCATTAAAA[A/C]AAAAAAACAAAAAAA | 55833 |
rs556631009 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005643 | GGGGAAATTTTTTTC[C/T]TGTAAAAAGGAAATA | 55833 |
rs556641583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012722 | TAAACTGTAGGGAAA[G/T]GAAGAGAACAGGATA | 55833 |
rs556661535 | snp | A/C | 0.00953873 | 0.0683987 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049167 | ATACAAGGTGCCCAC[A/C]ACTGCAGCTCGTCGT | 55833 |
rs556736828 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031603 | TGAGCCACCACGCCC[A/G]GCCTTAACTTGCTTT | 55833 |
rs556753178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042829 | ACACCTGTAATCTCA[A/G]CACTTTAGTAGGCCA | 55833 |
rs556774038 | snp | A/G | 1.65091e-05 | 0.00287303 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33998826 | TGAATCATTCTTATC[A/G]AAGATCACTTGAGCG | 55833 |
rs556787997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005037 | GGAGGCTGAGGCAGG[C/T]GGATCACTTGAGGTC | 55833 |
rs556803040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935427 | CGCCGCCACCACACC[C/T]GGCTAGTTTTTCGTA | 55833 |
rs556828601 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960067 | CCTGAGTAGCTGAGA[A/C]TACAGATGCACAACC | 55833 |
rs556876192 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935603 | CTGTATGCTGCACTT[C/G]TGGTGCAGTCTGATT | 55833 |
rs556888294 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959617 | CTTATTTTTCCAAAA[A/G]AAATACTATGCTGAA | 55833 |
rs556891803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987919 | GGAAGATGCCAACAC[A/G]CAGTCTTTTCTTTTT | 55833 |
rs556893714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995889 | GAAGTAATCAGAGGT[A/G]AGGACTGAGATGAAG | 55833 |
rs556894925 | in-del | -/AT | 0.125949 | 0.217051 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981304 | ATATATATTCTGGAT[-/AT]ATATATATATATCTA | 55833 |
rs556912613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950091 | TTTCTTTTTTGAGAC[A/G]GTCTCGCTCTGTCAC | 55833 |
rs556930611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995174 | CCAGTCTGGCCAACA[C/T]GGCGAAACCCCACCT | 55833 |
rs556932450 | snp | A/T | 0.000103187 | 0.00718211 | missense | UBAP2 | GRCh38.p7 | 9:33922599 | GCTGACCCGAGCCAC[A/T]CTGAGGAAGAGGAGA | 55833 |
rs556947297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943332 | GATAAACACTGAGGA[C/T]AGCTATTACCACAGG | 55833 |
rs556958048 | in-del | -/A | 0.170408 | 0.236992 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975802 | ACAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs556959093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963970 | TTATGAATCTTATCC[C/T]TGATGGCTCTTGGAC | 55833 |
rs556960908 | snp | C/T | 3.37941e-05 | 0.00411046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971800 | CAAAAGAAGCAAACA[C/T]CTAAGCCAAAATATT | 55833 |
rs556970115 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992485 | GAACTGCTTGAACCT[G/T]GGAGGCAGAGGTTGC | 55833 |
rs556970949 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966514 | TGCTAAGATTTTGAT[C/T]GGAATTGTGCTGAAG | 55833 |
rs556981090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982127 | AAGCTAAGCTTCAGG[A/G]AAGTCCTAAAAAAAA | 55833 |
rs556985244 | snp | A/G | 8.2969e-05 | 0.00644031 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927940 | ACGGAGGTCGCTGCC[A/G]TGGAGAAGGTGGCTG | 55833 |
rs556985916 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939535 | CAGCCATTTGTGTGC[-/TT]TTTATAAGACAAGAT | 55833 |
rs557030064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989987 | GAATTCTTCTAGTGA[A/G]AAGTCAAATAATTTA | 55833 |
rs557036593 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009458 | GGAGACAGGGTCTCG[C/G]TACTTGGCCCAGGAT | 55833 |
rs557062513 | snp | C/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922112 | ATTCTTCATTGGTAC[C/G]TGACCCCTATACCCA | 55833 |
rs557064720 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989419 | TGTTAGCCATGATGG[C/T]CTCGATCTCCTGACC | 55833 |
rs557103458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984259 | TCAGCATTAAGGAAG[C/T]ATCATCTAAGAAATT | 55833 |
rs557106518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996853 | TTTGGGAGGCAGAGA[C/T]GAGAGGATTGCTTGA | 55833 |
rs557111511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003153 | GCCTCTTAGGTTCAA[A/T]CAATTCTCATGCTTG | 55833 |
rs557111647 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990705 | CAATGGCACAGTCTC[A/G]GCTCACTGCAACCTG | 55833 |
rs557116278 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956740 | AACCAGGGCTCAACC[A/C/G]CAGACTCACTTCTCT | 55833 |
rs557129460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043516 | GCAAAGTATGATCCT[A/G]TTATTTATGGAGATA | 55833 |
rs557142112 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983791 | TACTTTACAGAAACC[A/G/T]GGTCCTAAATATAAA | 55833 |
rs557150069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999204 | ATAATAAAATCTTGG[C/T]GGGGCATGGTGGCTC | 55833 |
rs557181273 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932219 | CTCCCTTCTCCAACA[C/T]TGACCTTCTTGCAAT | 55833 |
rs557194633 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956896 | GCCGAGGCAGGAGGA[C/T]TGCTTGAGGCCAGAA | 55833 |
rs557224718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957389 | CCACAATTTCCACCT[A/G]TCCCTGTGGAATCAC | 55833 |
rs557231407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942711 | CCAGCCTGGACAACA[C/G]AGCAAGACCCTATCT | 55833 |
rs557233302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024368 | AAAATAGCAAATACA[C/T]TCTTTGAAAAATAAA | 55833 |
rs557241553 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977801 | CCGAGCGGCTGGGAT[C/T]ACAGGTGTGCATCAC | 55833 |
rs557277093 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017913 | GCCTTGGCGACAGAG[A/C]GAGACTCCGTCTCAA | 55833 |
rs557295399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017805 | GGTGGCAGGCATCTG[C/T]AGTCCCAGCTACTTA | 55833 |
rs557318826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955888 | AACTGCTAACAAATT[C/T]ATCAGTGGATACATC | 55833 |
rs557325565 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015444 | CCTGCCTCAGCCTCC[A/C]GACTAACTGCCATTA | 55833 |
rs557352470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971094 | AGGTGTGAGCCACCG[C/T]GCCCAGCTAAATTAT | 55833 |
rs557388497 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037654 | TAAGTAACAGCAGTA[A/G]TTATTTCTTGCTTAT | 55833 |
rs557389873 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035892 | GACATACTGCACATT[C/G]TCTCTTTTTTTTTTT | 55833 |
rs557404588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048618 | AGCACAGGGCAACGT[A/G]AGGGGAAGAGGAAGG | 55833 |
rs557433071 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018659 | ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 55833 |
rs557444378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997636 | TGTACTAAGTGAATG[C/T]CTGCAACATACAATT | 55833 |
rs557458998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941188 | AAGGGTAAAACTTTA[A/G]AACTATATCAAAAAT | 55833 |
rs557474142 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984553 | TGGTGGGGCTCATGC[C/T]TATAGTCCCAGCTGC | 55833 |
rs557519065 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042782 | TTTACTTTTTTTTTT[A/T]AATTTTACATATGGG | 55833 |
rs557526623 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036312 | AATAGAGATGGGGTT[C/T]CTCCATGTTGGTCAG | 55833 |
rs557539871 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034008 | CCCAAAGTCCTAGGA[G/T]TAAAGGCATGACCCA | 55833 |
rs557550512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030395 | CGGAGGTTGCAGTGA[C/G]CCGAGATCGCGCCAC | 55833 |
rs557557803 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004609 | AACACGGTGAAACCC[A/C/T]GTCTCTACTAAAAAA | 55833 |
rs557570805 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934075 | TTCCGCCAAGTCAGG[A/C]TGACTCTACCAATGC | 55833 |
rs557615410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978547 | CGAGGCCAAGGCAGG[C/T]GGATCACGAGATCAG | 55833 |
rs557646942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950035 | AGATCATTCTGAAAT[A/G]TAAGTTCTTCATCAA | 55833 |
rs557652416 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013248 | AATCCTGGTTTATAC[G/T]GATTCAAAAGAACTC | 55833 |
rs557657478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043424 | CACCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 55833 |
rs557659130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036931 | CAGCAATTCTCCCGC[C/T]TCAGCCTCCCAAGTA | 55833 |
rs557682886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024915 | CTTGAACCCGAGAGG[C/T]GGAGGTTGCAGTGAA | 55833 |
rs557708946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956259 | CTTCGCATAACAGCT[A/G]TTCTAAAGAAAATGA | 55833 |
rs557730226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934675 | CTCTCTCAAACAAAC[A/T]AACAAAATGGGGAGG | 55833 |
rs557750874 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971067 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 55833 |
rs557755401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003189 | ACAGGCATGCCACCA[C/T]GCCCTGCTAATTTTT | 55833 |
rs557789715 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977742 | ATCTTGGCTCACCAC[A/C]ACCTCAGCCTCCCAG | 55833 |
rs557789914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970343 | TGTTGACCCTCTTTA[C/T]AGTTTCTCTATTTAC | 55833 |
rs557825235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011676 | ACAGCTTGGGAAAAA[A/G]GAGGAAAAATCAGGA | 55833 |
rs557830827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996791 | TCACCATTTGGATTA[C/G]AACACTTCAAAGGCC | 55833 |
rs557841402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003701 | CGTGAGCCACCACAC[A/C]CGGCCAAAGAAAGAT | 55833 |
rs557850451 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017922 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 55833 |
rs557852461 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993228 | TGTTTCAGCACAGAG[G/T]AAGGTTAGATAATAG | 55833 |
rs557867792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996079 | AAACAGTCTTTTCAG[C/G]TAATCGTTCTTTCTG | 55833 |
rs557874597 | in-del | -/TAAA | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044865 | GCGAGACTCCATCTG[-/TAAA]TAAATAAATAAATAA | 55833 |
rs557909050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960741 | GCCAAGATCACGCCA[C/T]TGCATTCCAGCCTGG | 55833 |
rs557922955 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942007 | TTTAACTGAGAGATA[-/G]GGGGGACATCTTTAA | 55833 |
rs557923105 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968767 | ACAATTTGTGCAATC[A/G]TCACCTCTAATTCTA | 55833 |
rs557933619 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965558 | ACTATATCTTCTTTG[C/T]AAGTTGTACTTTCAG | 55833 |
rs557958623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004984 | ATTGAAAACAACAGT[C/T]GGGCATGGTAGCTCA | 55833 |
rs558009433 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024306 | AAAATTGCGCCATTG[A/C]ACTCCAGCCTGGGAA | 55833 |
rs558010984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997872 | CAAAACAAGATTTCA[C/T]TGTGAGACCTTTACT | 55833 |
rs558027223 | snp | A/C/T | 6.60266e-05 | 0.0057454 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963827 | GAGGGTTTAAACATA[A/C/T]GAAAAGAATGAAAGT | 55833 |
rs558056423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989839 | CCCCAAAAGCTCCAG[A/G]AATACAACCTTGCCT | 55833 |
rs558072917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023986 | GAGGCGGAGTCTGCA[A/G]GGAGCCGAGATGGCG | 55833 |
rs558082546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991041 | TGTAATCCCAGCACA[C/T]TGGGAGGCCAAAGCA | 55833 |
rs558085530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035648 | CGAGATCGTGCTACT[A/G]TACTCCAACCTGGGA | 55833 |
rs558140935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927367 | CAAAGAGAAATATAA[A/G]AAGAATCTGCCTCCT | 55833 |
rs558179833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013223 | TACTAAGTGCTAGAC[A/C]CAGGACAAAAATCCT | 55833 |
rs558227823 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039715 | ACACTGCAGAAGGCC[A/G]CAGGGACCTCTGCCT | 55833 |
rs558245711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955507 | CCTAGGCGACAGAGT[A/G]AGACTCCGTCTCAAA | 55833 |
rs558250984 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001299 | TACATACACATACTA[G/T]GGTAGCCTCCTAGTG | 55833 |
rs558265030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992663 | TATCGGGCGGAGGGG[A/G]GGGGGCACAAATAGG | 55833 |
rs558296060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007158 | GCAATCTAGACCCCT[C/T]TATTTCCTTCTCTTG | 55833 |
rs558299142 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947603 | GAGGTGGGCAGATCA[C/G]CTTAGTCCAGGAGTT | 55833 |
rs558313219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041140 | GGCACATCCTTACAA[G/T]GTAACCTCATACTAC | 55833 |
rs558324022 | in-del | -/GTTA | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953042 | ACTCAGCTAATTTTT[-/GTTA]GTTTGCTTTTTTCGT | 55833 |
rs558336412 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977233 | TATTAGAGACGGGGT[A/T]TCACCATTTTGGCCA | 55833 |
rs558339845 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992765 | GAAGTCTGCAAAGTA[C/T]ACACACATGCATACT | 55833 |
rs558377342 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007487 | GGTGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAT | 55833 |
rs558380573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940560 | AAGATAGGTGGATTG[C/T]GTGAACCCAGCAGTT | 55833 |
rs558383420 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000928 | GTACAGAAATTCAGT[C/G]TCTACCCTTACTGAA | 55833 |
rs558410561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021768 | CCTCCCAAGCAGCTG[A/G]GACTACAGACGCCTG | 55833 |
rs558421182 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956335 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTGGC | 55833 |
rs558423051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939648 | CCCCACTACTCGGGA[A/G]GCTGAGGTTGCAGGC | 55833 |
rs558472851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030174 | AGGTGAGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55833 |
rs558479994 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977317 | GCTGGGATTACAGGC[A/G]TGAACCACCGCGCCC | 55833 |
rs558558069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980921 | CACTGCACACCAGCC[C/T]GGGTGACAATGCAAG | 55833 |
rs558565236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957846 | GAGGAGACAGTAGGT[G/T]TTCATTTTCTTCAAC | 55833 |
rs558587713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044508 | AGGCAGAGGTTACAG[A/T]GAGCCAAGGCACCAC | 55833 |
rs558596086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955430 | AGGCTGAGGCAGAAG[A/C]ATCACTTGAACTCAG | 55833 |
rs558632092 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050181 | GTGTTAACAAGCTCT[C/G]AAGGTCCTCTAAACA | 55833 |
rs558635027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935341 | TTCAGACGGAGTCTC[A/G]CTTTGTAGCCCAAGC | 55833 |
rs558644559 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047816 | GAGACCATATCTCTA[A/C]AATTAATAGTAATTT | 55833 |
rs558676638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934867 | AGAACGACCAACGAA[C/T]CTCCAAACAGCCTTG | 55833 |
rs558692251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980536 | GTGAGCCACCGCACC[C/T]GGCGAGCGTCATTTC | 55833 |
rs558692746 | snp | A/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030447 | GAGCCAGATTCCATC[A/T]CAAAAACAAACAAAC | 55833 |
rs558710235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038669 | CTGCCTTGGCCTCCC[A/T]AAGTGCCGAGATTGT | 55833 |
rs558712308 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021220 | ATTTTTCTGTGTTAG[C/T]TGCACTAATATTAAC | 55833 |
rs558721944 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932873 | ACATCCATTTGCTCC[C/T]CAGATGCGAAAAGTG | 55833 |
rs558753803 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955835 | TACGTCTCAAAATAG[-/A]AAAAAAAAAAAAAAA | 55833 |
rs558772801 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031738 | TTCACTGAGCTGAGA[G/T]CACACCACTGCACTC | 55833 |
rs558772928 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972853 | ATAGGTATTTTGTCA[C/T]AACTTCAGGCGAAGT | 55833 |
rs558784327 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003345 | TGAGGTCCATTCTTA[G/T]ACCCAAATCTGTACA | 55833 |
rs558784891 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030165 | AAATCAGCCAGGTGA[A/G]CCGGGCGCGGTGGCT | 55833 |
rs558787992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924679 | AAGGAGGCAACAGAA[A/G]TGCAGGGGCCTGAAA | 55833 |
rs558818220 | snp | A/G | 0.000280022 | 0.0118293 | missense | UBAP2 | GRCh38.p7 | 9:33944480 | TGCAAAAGCTTGTTC[A/G]CAGTGGAGGGACTGT | 55833 |
rs558820066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930251 | GTTGAATCACTATGC[A/G]GGGCAATCTGCAAAT | 55833 |
rs558863787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030948 | AAATTAAACTAAAAA[A/T]AAAAATAAAATAAGG | 55833 |
rs558870848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929389 | CCAGAACTGGGAGTA[C/G]ATCAACCTGCTGAAT | 55833 |
rs558886165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985054 | TTGGAAAACAGTATG[A/G]AGATTTATCAAAAAC | 55833 |
rs558886866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979815 | GGAGGTTGCAGTGAG[A/C]CGAGATTGCACCACT | 55833 |
rs558897387 | snp | A/G | 0.000115608 | 0.00760201 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33998841 | AAAGATCACTTGAGC[A/G]AGACGCATCTGTTCA | 55833 |
rs558899479 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950934 | ACAAACACACACAGT[A/G]CCCAAATCCCAATCC | 55833 |
rs558899992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937631 | AAAAAAATTAAGCTG[A/G]GCACAATGGCTCATG | 55833 |
rs558943866 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025109 | TAAAAATGACTGAGA[A/C]ATGGAAACTAGACCG | 55833 |
rs559004801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991581 | CTTACTGAAGGAAGA[A/G]GTATAAGTCATTATT | 55833 |
rs559006059 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968394 | TTCCTCTGGTGATGA[A/G]GAAGCAAGACACCAC | 55833 |
rs559041061 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041053 | ATGTCCACATGAGGA[C/G]AAGTAAAATTGGTAA | 55833 |
rs559062463 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977724 | CTGGAGTGCAGTGGC[A/G]TAATCTTGGCTCACC | 55833 |
rs559075265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019357 | GCAGTGAGCCAAGGT[A/G]GTGCCACTGCACTCC | 55833 |
rs559119218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928697 | AACCCTAGCAACAGG[A/G]TCCTATGAAGAACTT | 55833 |
rs559125737 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929419 | TTAAAAAGTCAACAC[A/T]AATTTTCAAGGCTTC | 55833 |
rs559161349 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971047 | ACCTCAAGTGATCCA[C/T]CTGCCTCGGCCTCCC | 55833 |
rs559162162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012824 | CATTGCAACTTTTCC[A/G]TAAATCTCACAATGT | 55833 |
rs559178027 | snp | C/G | 0.000197655 | 0.00993922 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923271 | GTCTCCTGCTGCTGT[C/G]CCCTGGGTCAGGTCG | 55833 |
rs559178563 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050766 | CTTTGGGAGGCCAAG[A/G]CGGGCCGATCACGAG | 55833 |
rs559185155 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953167 | AGCCATCATGCCCGG[A/C]CTTACTGTAGATATT | 55833 |
rs559187024 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927434 | GGGACAGGCTGAGTT[C/T]GAAGTCGGTTTTAGC | 55833 |
rs559192818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006373 | AGAGCAATGCTTTGC[A/G]CAAGAAAAAATTAAT | 55833 |
rs559193635 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923431 | CTGGAAGGGAGGTGT[A/G]GGAGTGCTGAGGTTC | 55833 |
rs559234215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018934 | ATTATTCATAATAGC[C/T]AAAAAGTGGAAGATA | 55833 |
rs559234658 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922945 | AAAAACCTATACACC[C/T]AACCCACCTTTGTCC | 55833 |
rs559273271 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970437 | ATGTTTGTGTGCATT[A/G/T]TTTTTTTTTTTCAGG | 55833 |
rs559291194 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037113 | CCTGCCTCGGCCTCC[A/G]GATTAGCTGAGATTA | 55833 |
rs559300481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985119 | ATTAGCAGATATTTA[C/T]ACAAAGAAAAGGAAA | 55833 |
rs559305365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043046 | ACACTCCATCCTGGG[C/T]GACAAAGCAAGACCC | 55833 |
rs559307694 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957538 | CCTGGCTTCTTTCAC[C/T]CAGCATAATTATTTT | 55833 |
rs559336515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983379 | ACGATTTCTCTAAGA[C/T]GCCCACTAATGCCAG | 55833 |
rs559361534 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001510 | GGTAAAACTGGATTT[-/A]AAGGTTACAGCATGT | 55833 |
rs559413986 | snp | A/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942239 | ATCACTTGAACTCGG[A/G]AGGCAGAGGTTGCAG | 55833 |
rs559414458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977951 | ACCCGGGAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 55833 |
rs559428314 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954017 | GCTTAAGCGATTCTC[A/G]TGCCTCAGCCTCCCG | 55833 |
rs559430018 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949657 | GCAGTAAGGTGAGAT[C/T]GCACCACTGCACTCC | 55833 |
rs559534758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934986 | GCTTAAGTTCAATAT[C/T]CGCACTCCCAGGAAA | 55833 |
rs559569543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010681 | ATAATAAAGCATTGT[A/G]GGGAGGGATTTTGGC | 55833 |
rs559606637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005087 | GGCCAACATGGTGAA[A/G]CCCCGTCTACACTAA | 55833 |
rs559631314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017636 | TAAATCTTAAAGAAA[A/C]AATTGTGTGGCCGGG | 55833 |
rs559634181 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008088 | TGTAGTGAGCCGAGA[A/T]CGCGCCACTGCACTC | 55833 |
rs559638899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019661 | GTAACAATGGTTACA[A/G]TAAACTTTATGTTAT | 55833 |
rs559642552 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960605 | AAATGGTGAAACATC[A/G]TCTCTACTAAAAAAA | 55833 |
rs559668543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004701 | AGGCAGGACAATGGC[A/G]TGAACCTGGCAGGCG | 55833 |
rs559674234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973010 | ACCCTGCTCTAATGC[C/T]TGTTTAAAAGATCAA | 55833 |
rs559701647 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979302 | AAGACCAAAATAATA[C/T]ATATAAGCTGATAAA | 55833 |
rs559703184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962353 | TCAGGAGACATATTA[A/G]AAGTTTAAAAAAGGC | 55833 |
rs559709043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979429 | GAAAATACAAAATTA[A/G]CTGGGTGTGGTGGCG | 55833 |
rs559710965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972148 | CAAGTTTGGCTTTTA[C/T]AGCTTAGATTTATAT | 55833 |
rs559731950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980720 | AAGCACTTTGGGAGT[C/T]TGAGGTGGGCGGGTT | 55833 |
rs559738434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024089 | CAAGGATGGGCGCGG[C/T]GGCACACGCCTGTAA | 55833 |
rs559761680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042359 | GGCGGGCACCTATAA[G/T]CCGAGCTACTCGGGA | 55833 |
rs559801639 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029881 | AATCCCAGCTACTCG[G/T]GAGGCTGAGGCAAGA | 55833 |
rs559804736 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975236 | GGAGTTCAAGACCAG[C/G]CTGGCCAATATGGTG | 55833 |
rs559849983 | snp | A/G | 0.000263717 | 0.0114799 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927896 | TCATGCTACTGGACA[A/G]GCTGGCGCCTGAGGA | 55833 |
rs559858116 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921277 | ATGTTCAGTTGATGA[C/G]AAGCAAAAGACAGGT | 55833 |
rs559859002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011116 | CAAACAAGCACTTGA[C/T]GGGTGAAAGAATCTC | 55833 |
rs559861155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963022 | AAAAATAAAAAAGAC[C/T]GGCCTACCACTTTGA | 55833 |
rs559890891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930626 | ATGATGGCCGGGCGC[A/G]GTGGTTCACGCCTGT | 55833 |
rs559894162 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927202 | CAAAGAAGGGCAGTG[A/G]CCGAATGAGGCAGAG | 55833 |
rs559897433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927493 | CCTACAGACAGCCTA[A/G]GTCTGCAGTCGTGGA | 55833 |
rs559903936 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971240 | ACCTGCAGAGGCAAC[A/G]TTGCTACAAACCCAT | 55833 |
rs559912136 | in-del | -/ACTCCATTCAA | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974649 | ACTCGACAACAAAAT[-/ACTCCATTCAA]AATGGGCAACGGCCA | 55833 |
rs559918667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018097 | GAGGCTAAGATGGGA[A/G]GACTGCTTGAGCCCA | 55833 |
rs559920916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968086 | CTAACTTATCAGATT[A/G]CCCGGCAGTTACATT | 55833 |
rs559957426 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980302 | CAGTGGCGTGATCTC[A/G]GGTCACTACGAGCTC | 55833 |
rs559976346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994496 | CCCTAAACAAAGAGG[C/G]CGGTTAGGCTCTTCA | 55833 |
rs560017841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002081 | CTGACCTCAGCCTCC[C/T]GAGTAGCAACCATGG | 55833 |
rs560040196 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019421 | GGGGTAAAAAAAAAC[A/G]GACAAATACTACATG | 55833 |
rs560055507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008250 | TTGAACCCAAGAGGC[A/G]AAGGTTGCGGTGAGC | 55833 |
rs560055652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959759 | AGGTTGGGCATGGAA[C/G]CAGAGCAAACTTATT | 55833 |
rs560092552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044068 | TGCACTCTGGCCTGG[A/G]TGACAGAATGAAACT | 55833 |
rs560127142 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967052 | TCTTCTTTATTTTCT[C/T]TCAATATTGTTTTAT | 55833 |
rs560149186 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991815 | CAGAGGTCCTGGAAA[A/G]ATCATCCCAGAAGAG | 55833 |
rs560178784 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044604 | GTGTGGTGGCTCACG[C/T]AAGTAATCCCAGCAC | 55833 |
rs560182958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037766 | ACTTCAGTCACAATA[C/T]GTAAATACACAAACC | 55833 |
rs560209627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027545 | CAACACAGTGAGACC[A/C]CATTTCTATTATTTA | 55833 |
rs560252443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013460 | CGCACCATTGCACTC[A/C]AGCCTGGACAACAAG | 55833 |
rs560254936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966014 | GAGATCGTGCCACTG[C/T]GCTCCAGCCTGACTG | 55833 |
rs560266596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943947 | AAACAGGAATGGTTG[A/G]CATTAATATCACCAC | 55833 |
rs560298322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958979 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 55833 |
rs560327506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021854 | GGTCAGGCTGGTTTC[A/G]AACTCCAGACCTCGG | 55833 |
rs560344470 | in-del | -/TTTTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994462 | TTATTCCCAAAGATT[-/TTTTC]TTTTTTTTTTTTTTC | 55833 |
rs560362761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958093 | CTACTTCCTAAGTAG[C/G]TGGGACTACAGGCAC | 55833 |
rs560365986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045900 | ATATTCCCTACATGT[C/T]CTCCCTCTCTTTGCC | 55833 |
rs560410837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980259 | TTTTTTTGAGACGGA[A/G]TCTTGCTCTGTTGTC | 55833 |
rs560458973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046426 | AGGCAGGCGGATCAC[A/G]GGGTCAGGAGATCAA | 55833 |
rs560460995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953533 | TTACCAACAAATGAA[C/T]GTGAGAAGTCAATCA | 55833 |
rs560481158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005892 | TGAGAATATCAATCC[C/T]TAAATAATCAGTCCA | 55833 |
rs560487587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924564 | TGACACCACAGGCAG[A/G]TGCTTGTGTGAATGC | 55833 |
rs560536716 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946175 | CTTATAGACTGTTCT[C/T]ATCTCTTTAGCCAGT | 55833 |
rs560569589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006704 | AAAAGATAACGTAAA[C/G]AAAATGTGGGCCTAG | 55833 |
rs560569944 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986153 | CACCTCTTGGGTCCA[A/G]GCAATTCTCCTGCCT | 55833 |
rs560575762 | snp | C/T | 9.88468e-05 | 0.00702948 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986783 | CGGGCTCGCTTGCCA[C/T]GATCTGAAGGTTTGT | 55833 |
rs560642362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980620 | AGTACATTAAGTATA[C/T]TGATATCTTTTTCTG | 55833 |
rs560679254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980156 | GACATTCTAATAATT[C/G]CGCTTTAATCCAAAT | 55833 |
rs560694525 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024077 | AAATAGCAAATACAA[-/G]GATGGGCGCGGTGGC | 55833 |
rs560694684 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048300 | GAGTCCCAATTGAGA[C/T]CAATGCCCTACAGAA | 55833 |
rs560725047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032106 | GCTATGATCAGCCTG[A/G]GCAACATAGCATGAC | 55833 |
rs560739257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038430 | TGCGATTGCAGGCGC[A/G]CGCCGCCACACCTGA | 55833 |
rs560757601 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943892 | GACAACACGGCGAGA[C/T]CCTGTCTCATTTAAA | 55833 |
rs560762966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992804 | TTAACCAAGTAATTA[C/T]GGAGGATTTCCAAGA | 55833 |
rs560773088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013846 | CGCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 55833 |
rs560792832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026978 | GATGACAAAGATCTG[C/G]TCTAGATCAGATCTC | 55833 |
rs560794791 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021315 | TTTACATTATAGTAA[A/C]AACCAATTATCTAGA | 55833 |
rs560804675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993394 | GGCAACTAGGTAAGA[G/T]ATGAGGCAAACAGTA | 55833 |
rs560831369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008103 | TCGCGCCACTGCACT[A/C]CAGCATGGCGACAGA | 55833 |
rs560856863 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936388 | AAACTCCATCTCCCA[G/T]GTTCAAGTGATTCTC | 55833 |
rs560861403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33936466 | ACCAGGCTAATGTTT[A/G]TATTTTTAGTAGAGA | 55833 |
rs560873220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032077 | TTGATCCCAGGATTT[C/T]GAGGCTACAGTGAGC | 55833 |
rs560880702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014280 | TACAATGAGCCAAGA[C/T]AGAGTAACTGCACTC | 55833 |
rs560893552 | snp | A/G | 0.000822403 | 0.0202614 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935712 | GTCCAAAAACAAAAA[A/G]GCAAAAGGGCTGCTT | 55833 |
rs560896532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007589 | GAATTTTTTCACATA[C/T]ATTTTTCAGCGTTTA | 55833 |
rs560896838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924786 | CTGTCACCACCTACA[A/C]TGCTCTCAAAACACT | 55833 |
rs560929622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974369 | AATATTAATGGGGCA[C/T]AGTGGTACATGCCTG | 55833 |
rs560930221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930454 | AAGCAGAACTGTGGG[A/G]AAACAACAACAACAA | 55833 |
rs560984308 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970621 | GTTTTCTTAGTATAG[A/G]TGAGGTCTTACTATG | 55833 |
rs560997559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027429 | AAAAAATAAACAAAA[C/G]AATCTGGCCTGGCAT | 55833 |
rs561000488 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33924249 | ATCTCGGCTGGCAAG[C/T]GCTGTGGGTGCAGCA | 55833 |
rs561029122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973619 | GTAAGCTGAAGGCAC[C/T]GTTAAGTATCATTTT | 55833 |
rs561031549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957177 | AGATGTCTTTAGTAC[C/T]TAATTGATCAGTAAT | 55833 |
rs561031588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964770 | TTAATAAAAGCACTA[C/T]AATATCACATACAGA | 55833 |
rs561083645 | snp | C/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019575 | AGGGGAGGATACAAA[C/G]GTTCGGAAGATGGAC | 55833 |
rs561093701 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046955 | ATTGTTGTTCCAATA[C/T]AGTTCTAAAGGCAAC | 55833 |
rs561144174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958915 | GACCTTTGAGAAGCC[A/T]AGTCGGACAGATCAC | 55833 |
rs561176463 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937484 | GGGTGACACACACCT[A/G]TAGTTCTAGCTAGTC | 55833 |
rs561193287 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923164 | TCCAGGCCTTATCCT[A/G]GAAAGGAGAGGTAAA | 55833 |
rs561194357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957557 | CATAATTATTTTGGG[A/G]TATATGCACACTGTT | 55833 |
rs561205192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045290 | GGCGGAGCTTGAAGT[C/G]AGCCGAGATTGCACC | 55833 |
rs561221075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001442 | TGATTGGTGAGTGAA[C/T]ACGGTTGGTAAAACT | 55833 |
rs561248163 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943833 | GGACTTTGGGAGGCC[-/AA]GACAGGAGGATCATT | 55833 |
rs561269413 | snp | A/G | 0.000527018 | 0.0162244 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923339 | GAGCCAGGCAAGCCT[A/G]TCTAACCCCATGTGT | 55833 |
rs561312748 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930476 | CAACAACAACAACAA[A/C]AAACCCTTAAGTTTC | 55833 |
rs561316385 | snp | A/G | 0.000286887 | 0.0119734 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922825 | GGAGCCCAAGACCGA[A/G]GGCAGGCTGAAAGGT | 55833 |
rs561331266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046587 | AGGCGGAGCTTGCAG[C/T]GAGCCGAGATCAGGC | 55833 |
rs561352410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005871 | TCAATGAAAATACAC[C/T]GTCCTTGAGAATATC | 55833 |
rs561354670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018817 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCGCTCC | 55833 |
rs561357665 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976464 | ACAATTCCATTTACA[A/G]GAAATGTCCAGAACA | 55833 |
rs561394718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038413 | TCGGCCTGCCAAGTG[C/T]CTGCGATTGCAGGCG | 55833 |
rs561413116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005195 | TTGAACCCGAGAGGC[A/G]GAGGTTGCAGTGAGC | 55833 |
rs561420665 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002128 | CTAATTTGTTGTTGT[C/T]ATTTTCATAAAGACA | 55833 |
rs561424875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954517 | TACCTAACCTTGTAA[C/T]GAATGCCATTGAATC | 55833 |
rs561445852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951816 | CCTTCTTATCAATTC[A/G]GTGGACACACATAGA | 55833 |
rs561489341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960540 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGTGTATC | 55833 |
rs561495018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951056 | TTATTTGGAGACAAG[C/G]TATTGCTGTCAACCC | 55833 |
rs561496149 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001801 | ACCAGCAGATTCAGG[C/T]AGCCTTGTTCCAATC | 55833 |
rs561496410 | in-del | -/ACTCATA | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964232 | AAGGCTGAGTCCTGG[-/ACTCATA]ACTCTCTTATCAACA | 55833 |
rs561503270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999729 | GATTTTTTCTTTTTT[G/T]GAGATGGAGCCTCAT | 55833 |
rs561537608 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031456 | GGGATTACAGATGCC[A/C]ACCACCACACCTGGC | 55833 |
rs561544381 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009688 | TGGTCTCGAACTCCT[-/G]GACTCAAGCAATCCT | 55833 |
rs561551867 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015997 | AAAGTCTATTGTAAT[G/T]CAGGTATTTTACTAC | 55833 |
rs561573582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043974 | CTCTACAAAAAATAC[A/G]AAAATTATCAGAGCA | 55833 |
rs561584857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955192 | CTGTCAAAAAAAAAA[A/C]AAAACAGGTCTACAA | 55833 |
rs561590462 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952427 | CATACAGTACTAAAT[A/G]ACACTGTTTCAATAA | 55833 |
rs561599321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982906 | TTTGTTTTTGAGACA[A/G]AGTCTCACTGTCACC | 55833 |
rs561629527 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048754 | GACGAGCTGAACCCA[C/G]AATTAGAAAGCACAC | 55833 |
rs561667290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992195 | GGAGTTCAAGACCAG[C/T]CTGACCAACATGGAG | 55833 |
rs561668771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937736 | AACATGATGAAACCC[C/T]GTCTCTATTTAAAAA | 55833 |
rs561687464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016759 | GGCAGGGTTTCACAA[C/T]GTTGGCCAGGCTAGT | 55833 |
rs561689679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969443 | TCCAGCAGTAAGTAC[C/T]AGGGAGATTAAGGTG | 55833 |
rs561709671 | snp | A/G | 1.65312e-05 | 0.00287495 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996360 | ATCAGAAAATGGTTA[A/G]AGGCAAACAAAAAAC | 55833 |
rs561739760 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBAP2, SNORD121B | GRCh38.p7 | 9:33934362 | TTGGAAATAAAACAT[C/T]ATTGTCTTTTCCAGT | 55833 |
rs561790911 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987944 | CTTTTTCTCATCCCT[A/G]TATTGGCATTAATAG | 55833 |
rs561812802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009541 | TTGAGATTACAGGTG[A/T]TAGCCACCATGTCCC | 55833 |
rs561817386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033868 | AGCCTCCCAAGTAGC[A/T]GGGATTACAGGCACC | 55833 |
rs561858196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940116 | GAAGAAGGCCACGAC[A/G]ACAAGATTCCTTAAT | 55833 |
rs561913150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041378 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 55833 |
rs561917514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039266 | GCCGCCGCCCCGTCC[A/G]AGAGGTGGGGGGGGC | 55833 |
rs561919601 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940515 | AGTGTAGTGGCTCAC[C/T]CTATAATCCCAGCAC | 55833 |
rs561941374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028529 | GGATTACAGGCACCC[A/G]CCACCACGCCCGGCT | 55833 |
rs561945083 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038321 | CTCCCCACGGTCTCC[C/T]TCTGATGCCAAGCCA | 55833 |
rs561953921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034267 | TTAATACTTCAGAAG[C/T]TTTTCATTATAGTTC | 55833 |
rs561971069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989438 | GATCTCCTGACCTCG[A/T]GATCTGCCCGCCTTG | 55833 |
rs561995588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987349 | CCCAACAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 55833 |
rs562010355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926344 | GAGGAGGGAAGATAA[A/G]GACCAACATTTAACA | 55833 |
rs562045543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932056 | TGCTCACGGCTCCAC[A/G]ACCCACTGAGCCACA | 55833 |
rs562046622 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035949 | GTAGGTTAAGGCTGC[A/T]GTGAGCCTGATCGCA | 55833 |
rs562051071 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945662 | AATATATATAGACAG[A/T]CAGACAGACAGACAT | 55833 |
rs562065642 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945421 | GGCCCTATGACGTGA[A/C]CCCGGGAGGCGGAGC | 55833 |
rs562081619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994222 | AATACATAGCCCAGA[A/C]CCAGCTCCTTCAGGT | 55833 |
rs562103401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | UBAP2, SNORD121A | GRCh38.p7 | 9:33952828 | TATGTGCTTGGAAAT[C/T]ACCACATCATTGTTT | 55833 |
rs562118861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968239 | TAAACCCTCCATTGT[A/C]AACAGGAAGCTGGAT | 55833 |
rs562119259 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038873 | CCATCGTCTGAGATG[C/T]GGGGAGCGCCTCTGC | 55833 |
rs562125757 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027861 | AGCGAGACTCCATCT[-/C]AAAAAAAAAAAAAAG | 55833 |
rs562169580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938021 | TTTTTGTTTTGAGAC[A/G]GTGTCTGGCTCTGTC | 55833 |
rs562179086 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016206 | ATAGAAGGAAGAGGA[A/G]GAATAGGAGGAAGAG | 55833 |
rs562280323 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022627 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55833 |
rs562285976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981552 | AACAAAAAAAGCCTG[C/T]TACATTGTCCACTCT | 55833 |
rs562297028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938752 | AGTGAGCCAAGATCA[C/T]GCCATTGCACTCCAG | 55833 |
rs562305323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022105 | CAAAAATTAGCCGGG[C/T]ATGGTGGCGCACCTC | 55833 |
rs562323682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988117 | ATCTCTGTTTTTCCC[C/T]ATAACATAATTTCTA | 55833 |
rs562324712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925427 | AAACAACCCGAGGGA[C/T]AGAAAGAGCAACATA | 55833 |
rs562338884 | in-del | -/ATATATATATTAAATATAAAT | 0.0718919 | 0.175435 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995377 | TAAATAAATATATAA[-/ATATATATATTAAATATAAAT]ATATATATAAAGTAT | 55833 |
rs562350923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975270 | CCCCGTCTTTATTAA[A/T]AAAATGCAAAAATTA | 55833 |
rs562365293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021903 | CCTCCCAAAGTGCTG[C/T]AATTACAGACATGAG | 55833 |
rs562373493 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959612 | TTAACTTATTTTTCC[-/A]AAAAAAAATACTATG | 55833 |
rs562381076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942276 | AAGATCGCGCCACTG[C/T]ACTCCAGCCTGGCGA | 55833 |
rs562385882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983532 | ATTTTAACCAGAACA[A/G]GGTGGTAAGGACTAA | 55833 |
rs562388514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960457 | TTTCTTCCAAGCACC[A/G]AAGTCCCCACCAAAC | 55833 |
rs562398041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982163 | GCAGAACTGCCAGCA[A/G]CCAGCAGCCCCTCTT | 55833 |
rs562400821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988337 | AGTCTCAGGGTGATA[C/T]GTTAAATATTTACAT | 55833 |
rs562436255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975369 | CCCGGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA | 55833 |
rs562464601 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022476 | ACAGTCTGGCTTTGT[C/T]GCCCAGGCTGGAGTG | 55833 |
rs562474819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975733 | GCGTGAACCCGGAGG[C/T]GGAGCTTGCAGTGAG | 55833 |
rs562502533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954437 | CAACAATGAGCTACA[A/G]ACTTCCTGTACCAAC | 55833 |
rs562512654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002666 | CAGGTGTGAGCCACC[C/T]GCCCAGCCTTAACAT | 55833 |
rs562528126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038515 | GTCTCCAGCTGCTAA[C/T]CGCGAGTGATCTGCC | 55833 |
rs562550631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008772 | GAAATCGAGACCATC[C/T]TGGCCAACATGGTGA | 55833 |
rs562617068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038815 | GCGCCTCTTCCTGGC[C/T]GCCATCCCGTCTAGG | 55833 |
rs562618088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008305 | CGTGGGCAACAAGAG[C/T]GAAACTCCGTCTCAA | 55833 |
rs562654797 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991488 | GTACATATAGAAAGA[A/G]GTCCTTGATAGAAAA | 55833 |
rs562657178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040115 | GTTGAGCCAAGATCA[C/T]GCCATTGCACACTAG | 55833 |
rs562662327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946596 | CTTTGTGTCTCATCA[C/T]GTTGCCCAGGCTGGT | 55833 |
rs562684864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995485 | TATATAAATATATTT[A/G]TATTATTAAATATAT | 55833 |
rs562725841 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045224 | GGCGGCAGGCGCCAG[C/T]AGTCCCAGGTACTCG | 55833 |
rs562735635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937382 | GAGGCCAAGGAGGAC[A/G]TATCATTTGAGGTCA | 55833 |
rs562739895 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033737 | CAAGCATCAAATCAA[C/T]TCTTTTTTTTTTTTT | 55833 |
rs562744371 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943008 | CCATAGCAGCATCAT[C/T]CACTATAGTCAAAAA | 55833 |
rs562746645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034412 | AACTTTCTTAAAAAT[A/G]TCTGTTACCTAAAGA | 55833 |
rs562807669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003236 | GGGTTTCACCATGTT[A/G]GTCAGGCTGGTCTTG | 55833 |
rs562846995 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042477 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs562847976 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937908 | GGCAACAACAGCAAA[A/C]CTCCCTCTCAAAAAA | 55833 |
rs562861210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952707 | AGAAAGGGGTACTTT[C/T]AATCTCAAGAGTGAT | 55833 |
rs562868462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000660 | GGAAGAAAAGCCATA[A/C]GGAACTAATAAACAG | 55833 |
rs562880062 | in-del | -/T | 0.397127 | 0.202123 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012842 | ATCTCACAATGTATT[-/T]TTTTTTTTTTTTAAA | 55833 |
rs562882834 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945469 | GGCGCCACTGCACTC[C/T]AGCCTGGGTGACAGA | 55833 |
rs562916294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966808 | GATGGTTATAATTCT[A/G]TATGCATTTGTTAGA | 55833 |
rs563014365 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992888 | AAGAAACTCTAAGAG[C/G]AGAGGTCCTCCCAGC | 55833 |
rs563015369 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036365 | CAGGTGATCTGCCCG[A/C/T]CTCGGCCTCCCAAAG | 55833 |
rs563034721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981480 | ACCACCTCAGCCTCC[C/T]GAGTTTCTGGGACTA | 55833 |
rs563073139 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027804 | AGGCAAGAGCTTGCA[A/G]TGAGCCGAGATTGCA | 55833 |
rs563085343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040769 | CCCAATTCTTAGGGC[A/G]TCCACTCTGTGTATA | 55833 |
rs563091932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945355 | TACAAAAAAATTAGC[C/T]GGGTGTGGTGGTGGG | 55833 |
rs563102955 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019559 | GGTATGGAGTTTCTG[C/T]AGGGGAGGATACAAA | 55833 |
rs563107249 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044582 | TAAAAATAAAAGAAG[A/C]AGCCAGGTGTGGTGG | 55833 |
rs563141799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030690 | CCAGCACTTTGGGAG[A/G]CCCGGGCGCATGGAT | 55833 |
rs563153906 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036975 | GCATGTGCCACCACA[C/T]CCAGCTATTTTTTTT | 55833 |
rs563182355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041595 | CCAGCTACTCGGGAG[A/G]CCGAGGCAGGAGAAT | 55833 |
rs563207473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021364 | ACACTGGTTTAAAAC[C/T]TTTTACTGCATTTGA | 55833 |
rs563208892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928628 | CTGTGAAGAAAGAGT[C/G]AACCAGCGGATGCTC | 55833 |
rs563209306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987304 | ATAGTCCCAGCTACT[C/T]GAGAGGCTAAGGCAG | 55833 |
rs563236120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956279 | AAAGAAAATGAAATA[C/T]ACAAGTGACCATGAC | 55833 |
rs563243004 | snp | A/G | 2.08862e-05 | 0.00323151 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928039 | TGGAGGCAGAGGAGG[A/G]GGGTGCTGGGGAGAG | 55833 |
rs563245178 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934902 | CCCAACAATACCAGC[A/C]AATGTCAAACCAAAA | 55833 |
rs563323179 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962870 | GTAAATCCCGGCTAC[C/T]TGGGAGGCTGAGGCA | 55833 |
rs563329300 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990609 | ATTGTAACCTTTCTA[A/G]AAGGTTACTTAGAAA | 55833 |
rs563337070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048675 | GACCGTGGACCTGGC[A/G]AGTGAAGCTCGGCCC | 55833 |
rs563343080 | snp | A/G/T | 1.65021e-05 | 0.00287241 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953439 | GAGGCTTGACTGTGA[A/G/T]GAACAGGCTTCTGGA | 55833 |
rs563346690 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951382 | AGATAGAGTTTCTCT[C/T]GTCGCCCAGGCTGGA | 55833 |
rs563360641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988899 | CCTGTAATCCCAAAA[C/T]TTTGGGAGGCTGAGG | 55833 |
rs563388753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004264 | TTAAAATGGTCTATA[G/T]TTGGTGTAATTTTTA | 55833 |
rs563399705 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008273 | CGGTGAGCTAAGATC[A/G]CGCCATTGCACTGCA | 55833 |
rs563405788 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932133 | TTAAAGCTGGCGCGC[C/T]GACTCCAGCCCTCCT | 55833 |
rs563436336 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004583 | GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAC | 55833 |
rs563464301 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978267 | AGCTGGGTCTGGTGG[C/T]TCATGTCTGTAATCC | 55833 |
rs563475181 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973408 | CTGATACAACTACCT[-/A]TACCCAGTTAGTGAC | 55833 |
rs563491743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984002 | CTGCAGCCTCCACTT[C/G]CCCCAGTTCTCGTGC | 55833 |
rs563492155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991102 | CTATCCTGGCCAACA[A/T]TGTGAAACTCTTATC | 55833 |
rs563492274 | in-del | -/GTATGTATGTTAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999898 | TATGTATGTATGTAT[-/GTATGTATGTTAT]TTTGAGATGGAGTCA | 55833 |
rs563499158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017565 | CTGCCAATAGCCCAA[A/T]TTAAAATGTGTCAAG | 55833 |
rs563533204 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029222 | GAGAACTGAAAACAC[A/G]TTCACCTAAAAATGT | 55833 |
rs563550004 | in-del | -/CGCCAGGGCTGATTCGGCTGATCTGGCTGTCTAGG | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050006 | TGTCACCCCATAGAT[lengthTooLong]CGGGTGGCCCCTTCC | 55833 |
rs563561064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036011 | CTGTCTCAAACAAAA[C/T]AGAACAAAGCAAAAT | 55833 |
rs563569533 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966036 | GCCTGACTGACGAAG[C/T]GAGACTCCATCTCAA | 55833 |
rs563598971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926883 | TGCTCAGGGATGGAA[A/G]GGCAGCTCAAGGTGG | 55833 |
rs563607808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984559 | GGCTCATGCCTATAG[C/T]CCCAGCTGCTCAGGA | 55833 |
rs563658453 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983121 | CTGACCTCGTGATCT[A/G]CTCGCCTCGGCCTCC | 55833 |
rs563685173 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010454 | AAAAAAAAAAAGACA[A/G]TAAACAAATAATACA | 55833 |
rs563701041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939109 | GATTCTATTCCTGTT[C/T]GTGATTTTATGTCTC | 55833 |
rs563713862 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040979 | ACAAACCAAAAATTC[A/C]ACTCTCAGTTATGTA | 55833 |
rs563734665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947835 | GACTCAAAAAAAAAA[A/T]AAATAAAATAATAGA | 55833 |
rs563737965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933177 | GTGACATGGGCCCAG[A/C]GATGCCCAGAGAGGC | 55833 |
rs563741238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969739 | GGCATAGTGCCGGAC[A/C]CCTGTAATTCCAGCT | 55833 |
rs563801104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041492 | AAAAACAAACAAGAG[G/T]CCATGACCAGCCTGG | 55833 |
rs563810328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004012 | GGTATGAGCCACCAC[A/G]CCCAGCCCCAAATAT | 55833 |
rs563825107 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030709 | GGGCGCATGGATCAC[A/G]AGGTCAGGTGATCGA | 55833 |
rs563841649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029812 | GGCCAACATGGTGAA[A/C]ACCCATCTCTACTAA | 55833 |
rs563893690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955375 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 55833 |
rs563895232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940920 | AAACCAAAAAATTAG[C/T]GCAACTTTCTTTATT | 55833 |
rs563914393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977373 | TAAAAAATCTAATCC[A/G]TCGTCCCCATAAATT | 55833 |
rs563970969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961277 | TCAAAACAACAAATT[C/T]CATTTTAAGGCAAAT | 55833 |
rs563983796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948878 | ATGTTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55833 |
rs564064446 | snp | C/G | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934041 | TAAGAAGCTAACAGG[C/G]AAGACCACCTACACG | 55833 |
rs564073403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010380 | AGTGAGCCCAGATCG[C/T]GCCACTGCACTCCAG | 55833 |
rs564116749 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960989 | GATACATACGCCTCA[C/T]TAGCAATTTAGTTTA | 55833 |
rs564117861 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018634 | TTTGGGAGGCCAAGG[C/T]GGGAGGACCACAAGG | 55833 |
rs564126778 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035981 | CACTGCATTCCTGAG[G/T]GACAGAGTAAGACCC | 55833 |
rs564216435 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996445 | ACATGAAGATGGCCT[C/G]TTCTAGACTCTTGAG | 55833 |
rs564259248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983427 | TCAAATACCCTAGGA[A/G]AGAAAACCCTCTCCC | 55833 |
rs564291065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023498 | CTATTAAAATTTTAC[C/T]GGTCCATGTTCACAG | 55833 |
rs564293719 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036344 | ATGGTCTCAAACTCC[C/T]GACCTCAGGTGATCT | 55833 |
rs564302083 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968947 | ATACAATATATGTGG[-/TCTT]TCTGTGACTCTGCAT | 55833 |
rs564322181 | in-del | -/A | 0.158099 | 0.232496 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017018 | AAAAGAAAAAAAAGG[-/A]AAAAAAAAAAAAGAG | 55833 |
rs564334266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926380 | CATGGCCTACCAGGG[C/T]CCCAGGTCCCAAAGG | 55833 |
rs564407833 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990569 | CAATGAGGTATTATC[A/G]TACAGTTCTGGTGAG | 55833 |
rs564420973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982390 | CTTACTATCCAGCAA[A/G]GCCAACTGATCAAGC | 55833 |
rs564432360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030262 | CACCCTGGCTAACAC[A/G]GTGATACCCCATCTC | 55833 |
rs564449589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028569 | TATTTTTGGTAGAGA[C/T]GGGGTTCACCATGTT | 55833 |
rs564462962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938111 | AAGCCATCCTCCCAC[C/T]TCAGCTTCCCGAGTA | 55833 |
rs564474713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039957 | GAGGTCGGGAGTTCA[A/G]GACCAGCCTGATGAA | 55833 |
rs564490038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988547 | TATAAATGGAGAATA[C/T]AAAACAGCTTTATCT | 55833 |
rs564506157 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033893 | GGCACCCACCACCAT[G/T]CCTGGCTAATTTTTG | 55833 |
rs564515341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945559 | GAATATTATGTTTCT[C/T]TTCCACACCACTCTC | 55833 |
rs564518425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973411 | ATACAACTACCTATA[C/T]CCAGTTAGTGACTTC | 55833 |
rs564529615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987476 | TATGGTTGTGACAGC[C/G]TGCAGCTAGTAGTCC | 55833 |
rs564556381 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983479 | GGTTACTATGTATTC[C/T]TAAAACCTTAAGAAC | 55833 |
rs564558864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932111 | ACTCTTTGGCATATG[A/T]GGAAAATTAAAGCTG | 55833 |
rs564592482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938956 | CAGGCTGTGGAAGGG[G/T]AAGAGAAAAAGGAAG | 55833 |
rs564596450 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035470 | TCGCGCCACTGCACT[C/G]CAGTCTGGGTGACAG | 55833 |
rs564642482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968721 | AATCTATCCTTTTAC[A/G]ACAGACAGTTGAATA | 55833 |
rs564652801 | snp | A/G | | | intron-variant, nc-transcript-variant | UBAP2, SNORD121A | GRCh38.p7 | 9:33952822 | ATCAGATATGTGCTT[A/G]GAAATTACCACATCA | 55833 |
rs564680905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975951 | CCTGACATGGTGGCT[C/T]ACACCTGTAATCCCA | 55833 |
rs564691903 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011166 | ATAGTTATTAATAAT[A/C]GCATTTTGCTGTAGG | 55833 |
rs564692574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020312 | CTCCAATGATAACAA[C/T]GCAGAGCCAATGATT | 55833 |
rs564712901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982781 | AGAACCAAGGTAAAC[A/G]TATCAACTTTTTCCT | 55833 |
rs564737937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030753 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAGT | 55833 |
rs564743448 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950779 | TGCTTTACAACACAG[C/T]GAAATCACTGAATCA | 55833 |
rs564748147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984821 | TTACCCCAGTTAGAA[C/T]GGCTATTATCAAAAA | 55833 |
rs564753677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019875 | CAAAACAAAAACAAA[C/T]GTGCAGCCGGTCGCG | 55833 |
rs564754534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969561 | CTCTTTAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 55833 |
rs564760243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950989 | TAGAGACTTGGGAAA[C/T]ATCATCATCACTTCT | 55833 |
rs564786765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996931 | AAAAATTAACCGAGC[A/G]TAGTGGTAGGAGGAT | 55833 |
rs564808432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926851 | ACCACCAGGGCTCAG[C/T]GGGGCAGAGACGGGG | 55833 |
rs564816813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014184 | GCAAAAAAGTTAGCC[A/G]GGCATGGTGGCTCAC | 55833 |
rs564857271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032006 | AAAAATTAGCCAGGT[A/C]TGGTGGCGCATGCCT | 55833 |
rs564867130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935064 | AATAAAGAAAGAAAA[C/T]TACTATAAACCATCA | 55833 |
rs564876422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013668 | GATCACCTGAGGTCA[A/G]AAGTTTGAAACCAGC | 55833 |
rs564885371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037786 | ATACACAAACCCTGA[C/T]TGGATGGGAAAAGAG | 55833 |
rs564895143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031186 | GGAGGCTGAGGCAGA[C/G]GAATCGCTTGAACCC | 55833 |
rs564905872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942281 | CGCGCCACTGCACTC[C/T]AGCCTGGCGACAGAG | 55833 |
rs564926815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929724 | TAGCTCACATAGGCC[A/G]GGCACGGTGGCTCAC | 55833 |
rs564939811 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999979 | TTGAGATGGAGTCTC[A/T]CTCTGTCGCCCAGGC | 55833 |
rs564947870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026821 | AACCCAGGACATTTG[A/G]CTCTACAGTGTGTGC | 55833 |
rs564953296 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023944 | AGCTACCCAGGAGGC[A/T]GACGCAGGAGAATCG | 55833 |
rs564974748 | snp | A/C/T | 0.010335 | 0.0711961 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050917 | CAGGAGAATGGCGTG[A/C/T]GGAGTTTGCAGTGGG | 55833 |
rs564991680 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979538 | CAAGATCCCACCATC[C/G]CACTCCAGCCAGGGC | 55833 |
rs565019679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026086 | CTTTTCTAAAAACCA[C/T]GTATATACCCTAAAC | 55833 |
rs565024275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971926 | TCTGCCAGCCATGGA[G/T]ATGCAGATGTGAAAA | 55833 |
rs565107840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936315 | AAGGTAACTTTTTGA[C/G]ATGGTGTCTTGCGCT | 55833 |
rs565159914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966140 | TCCTTTAATATTATA[C/T]AAAAATTTTAGAGTC | 55833 |
rs565168271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006854 | GGGTTCAGACAATCA[A/G]AACGACTAGAGAAAC | 55833 |
rs565186162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048784 | CGCTGCAGCGCTCAG[A/G]GCCCTGGAAGAGGGA | 55833 |
rs565197223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991296 | ACAGAGCGAGACTCT[C/G]TATCAAAAATAATAA | 55833 |
rs565253992 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927435 | GGACAGGCTGAGTTC[A/G]AAGTCGGTTTTAGCA | 55833 |
rs565263126 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964474 | TTCAACATTCTGCTT[C/T]AACACTTGCACAACA | 55833 |
rs565265659 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045026 | TTAGTTATCAAAAAA[C/T]GGAAACTTATCAAAC | 55833 |
rs565279290 | snp | A/G | 5.10399e-05 | 0.00505147 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927975 | CTGGTGGGAAGAGGC[A/G]CTCTCCACACTGGCA | 55833 |
rs565279860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011200 | CAGTCTGGGGCTTAT[A/T]TATGTTTCTACATTA | 55833 |
rs565293852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024595 | CACAGGGGATGGGGG[A/T]TGTGACTGAAATCTT | 55833 |
rs565323116 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925641 | AGTGGGGAGAAGCCG[-/C]TCCGCTCCCAGGCTA | 55833 |
rs565341847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030168 | TCAGCCAGGTGAGCC[A/G]GGCGCGGTGGCTCAC | 55833 |
rs565347052 | snp | C/T | 1.8103e-05 | 0.00300852 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922675 | GGTGGCTGCCTCCAT[C/T]ACTGTACTCACCTGT | 55833 |
rs565360697 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012346 | GAGCAGCCTGGCCAA[C/T]ATGGCGAAACCTCGT | 55833 |
rs565385705 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922019 | ACAGATGACAAACGG[A/G]ACAGTTTCTCAAAAA | 55833 |
rs565386057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956401 | TCGGCTCACTGCAAT[C/T]TGTGCCTCCTGGGTT | 55833 |
rs565398959 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947597 | GAGGCCGAGGTGGGC[A/G]GATCACCTTAGTCCA | 55833 |
rs565420600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018788 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 55833 |
rs565435893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957048 | GAGCCATGATCACAC[A/C]ACTGCACTCCAGCCT | 55833 |
rs565457799 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954206 | GCCACCCTACCTGGC[A/C]AAGTTTCATATTTAT | 55833 |
rs565461405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927692 | ACACGCAGCGCACTC[A/G]GCGGGCCTGAGACTC | 55833 |
rs565465883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043220 | TCTGTCACCCAGGCT[C/G]AAGTGCAGTGGCACA | 55833 |
rs565537379 | snp | A/G/T | 0.000426416 | 0.0145966 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922405 | TGGCTGACACATGTC[A/G/T]GGAATTCTAGGAAAG | 55833 |
rs565552304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037231 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCCCC | 55833 |
rs565554594 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928335 | ACTTCGGATCATAAA[A/T]GAACACAGACTATCT | 55833 |
rs565592179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950178 | TCACTCCATTCTCCT[C/G]CCTCAGCCTCCCGAG | 55833 |
rs565594414 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028187 | CATGGATATAACCTG[C/G]CCATGGAAAGGATGA | 55833 |
rs565598879 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049603 | AGCGAGAGCCTCGGC[A/G]AGGCGGAAGGTGCGC | 55833 |
rs565601349 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973547 | AAAGAGCTAACACCA[C/G/T]GGAATTATAAGCCAC | 55833 |
rs565604148 | in-del | -/GTAAAGCAGTGAGAAAGGTTAGGGA | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978847 | ATACAAAACAGTAAG[-/GTAAAGCAGTGAGAAAGGTTAGGGA]GTAAACTATTGTTGC | 55833 |
rs565631739 | snp | C/T | 0.000412477 | 0.0143551 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933623 | GAGGGCCTGTTGTCT[C/T]TGGAGCTGGAACAGA | 55833 |
rs565660079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934471 | CAAACATAAGCAATG[A/C]AAGGGTCAACTTACA | 55833 |
rs565664024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017796 | GCCGGGCATGGTGGC[A/G]GGCATCTGTAGTCCC | 55833 |
rs565676037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984028 | CGTGCCTCAGCGTCC[C/T]GAGTAGCTGGAACTA | 55833 |
rs565780941 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955196 | CAAAAAAAAAAAAAA[A/C]CAGGTCTACAAAAGT | 55833 |
rs565813200 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003686 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACA | 55833 |
rs565825777 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003121 | CAGTAGTGTGCTCTC[A/G]GCTCGCTGCAACCTC | 55833 |
rs565844204 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990761 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGGTTA | 55833 |
rs565872342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012568 | GACCATTGAAAAAAT[A/G]TAAGTATGGTCTGTA | 55833 |
rs565954613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016515 | CAAGTACAATACCTC[C/T]TTCCTTACTATTCTT | 55833 |
rs565955903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005397 | CCTAGATCATGCCAT[A/T]GCACTCCAGCCTGGA | 55833 |
rs565958292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969025 | CTTTTTATGGCTGAA[C/T]ATTATTCCATTCTAT | 55833 |
rs565986263 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961597 | TACAGCATGTATGAA[A/G]AAAATGCCCATAGAT | 55833 |
rs566017101 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017101 | TGCTGAAATCTGTGG[G/T]TTTTCCCGAGCACCT | 55833 |
rs566019823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004883 | TGAGTCAGGAGGAGA[C/T]CAGCCTGGGCAACAT | 55833 |
rs566033095 | snp | C/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997450 | AGCAAAGCCCATCTA[C/G]AACCCAGGCCTCCTG | 55833 |
rs566071616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960710 | GCTTGAATCTGGGAG[A/G]CAGAGGTTGCAATGA | 55833 |
rs566113875 | snp | C/T | 1.65081e-05 | 0.00287293 | missense | UBAP2 | GRCh38.p7 | 9:33926654 | ATCTGGAGCTCGTCA[C/T]AGCCATAGATCTGTG | 55833 |
rs566175917 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934954 | ATTACAGTTTCAACT[A/G]AGGCTCACCTCGGTC | 55833 |
rs566182425 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041091 | AAACTGGAAATGAGA[C/T]AAATATCCATCAACA | 55833 |
rs566241587 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041765 | GCAGTGGCTCATGCC[A/T]GTAATACCAGAACTT | 55833 |
rs566280927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955478 | TGAGCCGAGATCGTG[C/T]CACTGCACTCCAGCC | 55833 |
rs566292435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989337 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCGCCTGC | 55833 |
rs566294862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001523 | TTTAAGGTTACAGCA[C/T]GTCATTGTGGCAGCT | 55833 |
rs566296126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34013989 | AATGAATAAATAAAC[A/G]TCAATAATTTTCCTA | 55833 |
rs566323926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048294 | AAAACTGAGTCCCAA[C/T]TGAGACCAATGCCCT | 55833 |
rs566370329 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987584 | ACTGCACTTCAGCCT[G/T]GGTGAAAGAGTGAGA | 55833 |
rs566435971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958413 | CTGAATGGTTCCCCA[A/C]CCCCTTTTTTTTTTG | 55833 |
rs566468040 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029473 | GGCGGAGGTTGCAAT[A/G]AGCCAAGATTATGCC | 55833 |
rs566472857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965595 | TGTTTAAGTGTAACC[C/T]TGGAGGGTAATTTTT | 55833 |
rs566478049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993725 | CTCTACTTCTGTCCC[C/G]CACAGCCCACTCAGC | 55833 |
rs566484982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007106 | CTAAATACAACATGT[C/T]ATCTATAAATAAGAA | 55833 |
rs566523944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044905 | GAGTATTACCTAGTC[G/T]TAAATAAAACACCTA | 55833 |
rs566532986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949971 | CAAAGAGAATGAAAG[C/T]CTATGACTAGAAAAG | 55833 |
rs566552707 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987685 | CTGAAAATAAATTAA[-/C]ATACTGATTTTTCTT | 55833 |
rs566608689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987037 | TTACACTTGTAATTC[A/C]AGCACTTGTAATTTC | 55833 |
rs566635727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032459 | CCCAAGGCTTCACAG[A/G]AAAGGGGATAAAGGA | 55833 |
rs566640619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952901 | TAGAGACAGGGTCTC[A/G]CTCTGTCACCCAGCC | 55833 |
rs566696613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038629 | GCGTGATCTCGGCTC[A/C]CTACAACCTCCACCT | 55833 |
rs566710371 | in-del | -/AGG | 0.021333 | 0.101051 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955279 | TAATCCCAGCACTTT[-/AGG]AGGCCGAGGCTGGCG | 55833 |
rs566722401 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043243 | GTGGCACAATCACAG[A/C]CCACTGCAGTCTCAA | 55833 |
rs566734148 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939867 | GGGAGGGGGAGGAGG[A/G]GGAGGAGGGGAGGAG | 55833 |
rs566745570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979072 | CAGAGACCTGCCTAC[A/G]ATGCTTTTGAAAATT | 55833 |
rs566752783 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944797 | TTCATTTATGATAAA[C/T]GGGAAAAGTTCCTAA | 55833 |
rs566759047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957302 | AAACCAAATAACTGA[A/G]TAAGTCTGGCATACA | 55833 |
rs566764558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943236 | GAGACAGATTATTGG[C/T]TGCTAAGGGGCAGGG | 55833 |
rs566783694 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989964 | CACCTAAATTTTTAA[A/C]CTCCAAAGAATTCTT | 55833 |
rs566817176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038093 | TCATCTGAGCACGGG[A/G]AGTTCAAGGCTGCAA | 55833 |
rs566821568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973293 | TGTCCTACACAATTA[C/T]ACTTCCTTCTTCATC | 55833 |
rs566910880 | snp | A/C | 1.64833e-05 | 0.00287078 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935778 | CACATCACGTGAGCT[A/C]TCCTCTTCCTCTGTT | 55833 |
rs566920480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985032 | AATATAAACTGGTAC[A/G]GCCATTTTGGAAAAC | 55833 |
rs566920662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030832 | CAACCCAGAAGGCTG[A/G]GGCAGGAGAATGGCA | 55833 |
rs566941603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979639 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 55833 |
rs566952113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992312 | AGAATCGCTTGAACC[C/T]GGGAGGCAGGAGGTT | 55833 |
rs566953346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031598 | AGGCATGAGCCACCA[C/T]GCCCGGCCTTAACTT | 55833 |
rs567013328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928915 | ACTAACTCTCCGCCG[C/T]CATCCCATGCCCACA | 55833 |
rs567014350 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990299 | AAAATTTGACATTAT[A/G]TATCCAAAGTAAACA | 55833 |
rs567023839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985425 | AATCAACCTAAGTGT[C/T]CATCAACAGATGAAT | 55833 |
rs567058554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026240 | CTACATACTTACACT[A/G]CATGTATTTAAGACA | 55833 |
rs567071201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025742 | AAAAGTTTTGTTTCC[A/G]TTTTTGTTTTCTTTT | 55833 |
rs567073372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929254 | ATGAACATTCTCCAT[C/T]GCTAAGAGATGCTCA | 55833 |
rs567084894 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005235 | ACCACTGTACTCCAG[C/T]CTGGGCAGCAGAGTG | 55833 |
rs567100354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935332 | TTTTTTCTTTTCAGA[C/T]GGAGTCTCACTTTGT | 55833 |
rs567148860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019899 | GGTCGCGGTGGCTCA[C/T]ATCTGTAATCCTAAC | 55833 |
rs567173896 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044659 | CACCTGAGGTCAGGA[A/G]TTCCAAGACCAATAT | 55833 |
rs567259278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929228 | ACAACCTTTTAATCT[C/T]GGAAGGAAAAATGAA | 55833 |
rs567264021 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019276 | GGCATGGTGGCACAC[A/G]CCTGTAATCCCAGCA | 55833 |
rs567272235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972638 | GCTAATGTTTTAGAA[A/G]CAACAAAAAGTAAAA | 55833 |
rs567279080 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973203 | GCCTTGGGTTGAGAA[C/T]CTTCCTGCCCCTCTC | 55833 |
rs567287439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956466 | TGGGCCTCCAGGCAC[A/G]CACCAGCATGCGCCA | 55833 |
rs567296330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928882 | GGCCCAGGAGAAGGA[C/T]CCAACCTGCCTGCGC | 55833 |
rs567328473 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050477 | TTGTACAGGGCACTA[G/T]GCTAATTACTAATTT | 55833 |
rs567329450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044739 | AGTGTGTTGGCAGGC[A/G]CCTGTAACCCCAGCT | 55833 |
rs567415705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000140 | TTTTTTAAAGGTAGG[A/G]TCTCATTCTGTCCCC | 55833 |
rs567417291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038607 | TTGCCCAGGCTGGAG[A/T]GCAGTGGCGTGATCT | 55833 |
rs567432975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958331 | AATTAAATCGATTTA[C/T]GAAAAAGAGAAAAAA | 55833 |
rs567436137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038240 | AAGATCATGAGGTCA[A/G]GAGTTCAAGACCAGC | 55833 |
rs567469917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957698 | CTGGAAAATGTTGAT[C/T]TAATGAGGTAACACG | 55833 |
rs567471064 | snp | C/T | | | missense | UBAP2 | GRCh38.p7 | 9:33941753 | ACATTGCTACTGGAC[C/T]AGCAGAATTCAGTGA | 55833 |
rs567471322 | snp | A/G | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934229 | TGTGCTTGAATAGAT[A/G]TATCTCAGAGCACAT | 55833 |
rs567497594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000833 | CTCCAGGTGCTTTGG[C/T]CTGTTCATCCCAACC | 55833 |
rs567510095 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943905 | GACCCTGTCTCATTT[A/G]AAAAAAAAAAGGAGA | 55833 |
rs567541814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33952125 | CGATTTGACTCGGGA[A/G]AAAATTCTGTTTCTC | 55833 |
rs567551955 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045410 | GAGACGGAGTCTTGC[-/T]CCATCCAGGCTGGAT | 55833 |
rs567571367 | in-del | -/ACTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967308 | TTTCCAATCCTTATG[-/ACTT]ACTTATTTTTTCTTT | 55833 |
rs567574986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978911 | ATTATTTTTCTTCCA[C/T]CCAGAAGGAAACCAA | 55833 |
rs567596938 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037867 | ATGGGAAAGAGGCTA[C/T]AAAAATACATTTTGT | 55833 |
rs567608696 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935174 | GTGGCGGGGGGGGGG[-/GG]TCTCATTTTCTCCCA | 55833 |
rs567614503 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964713 | AGACCCCCATCTCTT[-/A]AAAAAAAAAAGAAGC | 55833 |
rs567618428 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023088 | AAAATTAGCCAGGCA[C/T]GGTGGCACGCGCCTG | 55833 |
rs567632445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042565 | GGCCAAGCAGGAGGA[A/T]CACTTGAGTCCAGGA | 55833 |
rs567659890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984888 | GCTGAAACAGGAAGA[C/T]TGCCTGAACCCAGGA | 55833 |
rs567662736 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042459 | CTTCAGCCCAGGCGA[C/T]AGTGCAAGACTCCGT | 55833 |
rs567682795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953897 | CTGCAGTAAGCAATT[A/C]AATAAGTTTCACTTT | 55833 |
rs567696267 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34048951 | TGACCTCGCGTCACG[G/T]GCGAAGGAGGAGCCA | 55833 |
rs567705539 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046376 | GGCTTCATGCCGGGC[C/G]GGGTGGCTCACGCCT | 55833 |
rs567717501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957140 | AAAGGTGAAATAATC[A/G]ATGTTTTCTCCCCCC | 55833 |
rs567719415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959941 | AACACCTGGTAAATT[C/T]TGTTTGTTTGCTTTA | 55833 |
rs567719583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953095 | GTCTGGTTTCAAACT[A/C]CTGGGTTCAAGTAAT | 55833 |
rs567720542 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942436 | ACTAAAACAACAACA[A/G]CAACAAAGTCAGCCA | 55833 |
rs567730192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036715 | GCATATACCATTTGC[A/G]CAGGGAGAACCATCA | 55833 |
rs567736859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991434 | AGTCTAGTGTATCCA[C/T]AAATGGAGCAGTATG | 55833 |
rs567751968 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925558 | AAGCAGAATGAATCC[C/G/T]GGGGCTCAGCACCAC | 55833 |
rs567795310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998399 | TGAGACCACGTCTCT[A/G]TGAAAAAAAAATTTT | 55833 |
rs567810902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934699 | GGGGAGGGAAGGGGA[A/G]GAGGAAGTGAGGGAG | 55833 |
rs567843501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030795 | ATTAGCTGGGCATAG[C/T]GGCAGGCGCCTGTAG | 55833 |
rs567884534 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985938 | AAGTAGGAGGATTGT[G/T]TGAGCCCAGGAGGTG | 55833 |
rs567891935 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973849 | AGCAATGATTTCTTG[A/T]GTATGACACTAAAAC | 55833 |
rs567892495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981824 | TGGAAGGGGGGAAGC[A/G]GGGAAGGAGGGAAGG | 55833 |
rs567902599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037336 | GGTAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55833 |
rs567941355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039614 | AAATGGATAAAGGGC[A/G]GTGCAAGATGTGCTT | 55833 |
rs567950132 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953683 | CAGGGTTTTGCAGAG[-/A]AGAGAATCAAAAGGT | 55833 |
rs567953100 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000554 | ATCTAAAATTACTCC[A/G]AAATAGTTTAAGTTG | 55833 |
rs567965424 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998351 | TGCAGTGAACTATGA[A/C]AGCACCACTGCACTC | 55833 |
rs568022360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002229 | AAAGAGCTGGAATTA[C/T]AGGCATGAGCCACCA | 55833 |
rs568086907 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008383 | AATCTAATTCTACCA[A/C]CTTCTGGTTCCCTTT | 55833 |
rs568086993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001699 | GTTAGTGTCCCTGTT[A/G]CAAGAAGCCTGTATG | 55833 |
rs568104407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027190 | CTCAGATTAAGAATC[C/T]GAGGCCAAGGCCAGG | 55833 |
rs568106167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033265 | TACTTATACACAACA[G/T]AGTACTACTTAGCCA | 55833 |
rs568112662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995629 | TATTTATAAATAAAT[A/C]TATACATATGTATAA | 55833 |
rs568165054 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939393 | TAGTAGAGACAGGGT[C/T]TCACCATGTTGCCCA | 55833 |
rs568176814 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935553 | TTATGGGCATCAGCC[-/A]ACCCCGCCTGGCCCA | 55833 |
rs568207863 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939254 | GCTGGAGTGCAACGG[C/T]GTGATCTCCACTCAC | 55833 |
rs568239534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930081 | AATGGTTTTCAAATA[C/T]ATAAAAAAAAGGATG | 55833 |
rs568243845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027611 | GCCTGTAATCCCAGC[A/G]CTCTGGGAGGCCAAG | 55833 |
rs568248528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034565 | AGAAATACCCCACAT[C/G]CTTATATGTCTAAAG | 55833 |
rs568255251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028791 | TTATAACAGTTCTCT[A/C]TCTCCTACAAAAAGG | 55833 |
rs568265915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028255 | TATTTGATATCGTCA[C/T]AATTCTCTTTCAGGT | 55833 |
rs568291497 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023094 | AGCCAGGCATGGTGG[A/C]ACGCGCCTGTAGTCC | 55833 |
rs568400703 | snp | A/C | 0.000164951 | 0.00908011 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944362 | TCATGATGAAATGCC[A/C]ACCTTAGAAGCTGGG | 55833 |
rs568403580 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959134 | GCCTGGTGACAGAGC[A/G]AGAGCAAGGCCCTGT | 55833 |
rs568442099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986436 | TTAGCAATAAAGTAT[C/T]TTTAAAATAAGGTTT | 55833 |
rs568448852 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930875 | CACTCCAGCCTAGGC[A/G]ACAGAGTGAGACTGC | 55833 |
rs568482015 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959170 | AAAAAAAAAAATTAA[A/C]GTACTTATTTTTTAC | 55833 |
rs568488013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959079 | ACTTGAACCCAGAGG[C/T]GGAGGCTGCAGTGAG | 55833 |
rs568492483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974153 | TATGATCAAACCACT[A/G]TATGCAAGCCTGGGT | 55833 |
rs568513877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014705 | AAGGCTGAGGCAAGA[C/G]AATCACTTGAACCCG | 55833 |
rs568517760 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980792 | AAAACCCTCTCTCTA[A/C]AAAAATTAGCTGGGC | 55833 |
rs568522932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967035 | TATCCCTCTATTTAT[A/T]GTCTTCTTTATTTTC | 55833 |
rs568546491 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943735 | GAAAATAGGCTAAGA[C/T]TTTTCTAAAAAGAGA | 55833 |
rs568563076 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005374 | GGGAGGCAGAGGGTG[-/C]CAGTGAGCCTAGATC | 55833 |
rs568564320 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937470 | AAATTAGCTAGGTGG[C/G]GTGACACACACCTGT | 55833 |
rs568568236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020753 | CAAGCTCTGCTTCCT[A/G]GGTTCACGCCATTCT | 55833 |
rs568574587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974768 | ACCAACCTGGCCAAC[A/G]TGGCAAAACCCCATC | 55833 |
rs568580086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993825 | ACAAGAAGTCAGATA[C/T]AGCCCACACTATAAA | 55833 |
rs568605162 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039262 | CCTGGCCGCCGCCCC[A/G]TCCGAGAGGTGGGGG | 55833 |
rs568684876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967291 | CAACGGTTTATTCTC[C/T]CTTTCCAATCCTTAT | 55833 |
rs568692305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994647 | TTCAAAATTTTAATT[C/T]ATCATATAATATGGT | 55833 |
rs568692359 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987094 | CCCAAGAGCTTGAGA[A/C]CAGCCTGGGCAACAT | 55833 |
rs568724628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968414 | CAAGACACCACCACC[A/C]GGGCATACATAGTCA | 55833 |
rs568793634 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000984 | AATGTAAGGACCTTA[A/C]ATATACTCTCACTAT | 55833 |
rs568793828 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012227 | TATATTCCACAATCT[A/G]ATTAGCTAAAAAGGA | 55833 |
rs568844982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952921 | GTCACCCAGCCTGGA[A/G]TACAGAGGCATGATC | 55833 |
rs568854585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987600 | GGTGAAAGAGTGAGA[C/G]CTTGTCTCAAAAAAA | 55833 |
rs568855483 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033950 | CATGTTGGCCAAGCT[G/T]TTCTTGAACTCCTGA | 55833 |
rs568856867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007160 | AATCTAGACCCCTTT[A/G]TTTCCTTCTCTTGCC | 55833 |
rs568867172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045055 | ACATTGTTTACAAAC[C/G]GGTAAAAAAAGGCTG | 55833 |
rs568870718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943275 | AAACTGAGACTGTCT[G/T]CTACAGGTATGGGGT | 55833 |
rs568891381 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014607 | GCACTCCAGCCTGGG[C/T]GACAGAAGGAGACTC | 55833 |
rs568904461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001629 | CTAAATTTAGTTGGG[A/T]ATGACAAGATAACTC | 55833 |
rs568932026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039014 | CTGCCCGGCCGACCC[A/G]TCTGAGAAGTGAGGA | 55833 |
rs568938902 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939715 | GAGCCAGACCCTGTA[A/T]CAAAATGAAGAAGAG | 55833 |
rs568959420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038124 | TGAGCTAGGATTGCA[C/G]CACTGCACTCCAGCC | 55833 |
rs569005544 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945014 | TCATGCCTATAATGC[A/C]AGCACTTTGGGAGGC | 55833 |
rs569011735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981756 | GGGATGGAAGGATGG[A/C]AGGTAGGTAGGTAGG | 55833 |
rs569024654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937643 | CTGGGCACAATGGCT[C/T]ATGCCTGTAATCCTG | 55833 |
rs569025186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935983 | AATCAAGAAACAATT[A/C]TCTCTTTTATTCTAT | 55833 |
rs569026146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028216 | GAGTGCTGGTGAACT[C/T]AAACACTATAGGACA | 55833 |
rs569031112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944151 | CAGATCTTCAAATCT[A/G]TACTTGAAATAAGGA | 55833 |
rs569080863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953702 | GAATCAAAAGGTGTA[C/T]TGAGAAATTTTCAAA | 55833 |
rs569105151 | in-del | -/ATATATAT | 0.00438332 | 0.0466095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981104 | ATATATATATTCTGG[-/ATATATAT]ATATATATATATATA | 55833 |
rs569115182 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961854 | ATAACTGACCTCCTC[A/C]TAAGTAAAATGATGA | 55833 |
rs569117175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033363 | AATAACCCAGAAACA[G/T]AAAGACAAACATCAC | 55833 |
rs569119006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039446 | AGATAGAGAAATCAG[A/G]TTGTTGCTGTGTTTG | 55833 |
rs569127090 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959767 | CATGGAACCAGAGCA[A/G]ACTTATTCAGGTTAA | 55833 |
rs569152349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014142 | CCAGCCTGGCCAACA[C/T]GGTGAAACTTCATCT | 55833 |
rs569197200 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958805 | GATCCCTTGAGCACA[-/G]GAGTTTGGGGCTGGA | 55833 |
rs569207291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966542 | AAGCTATCGATCAAT[C/T]TGGAGAGAAATGACA | 55833 |
rs569222320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031717 | TTGAATGTATGAGGC[C/T]GAGGCTTCACTGAGC | 55833 |
rs569227399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032298 | GAACAAATTAACTCA[C/T]AGATTTAATACCAAC | 55833 |
rs569248235 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050502 | TAATTTGCTAGTTAT[C/T]AAGTAAAACAATTGA | 55833 |
rs569262009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940403 | GCTTAAAAATTTACT[C/G]AGAAACCTTGGACAT | 55833 |
rs569292315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979821 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC | 55833 |
rs569308885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026426 | ACATAATGGGCTAAG[A/G]GTTCAACTACTAAAA | 55833 |
rs569329705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986389 | GCAAAAAGACTACAA[C/T]TCACTGAAAGCTCAA | 55833 |
rs569355681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035321 | CAGCCTGGCCAACAT[A/G]GTGGAACCCCATCTC | 55833 |
rs569362308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027004 | ATCTCACCTAGCTTC[C/T]CAGCCTTTCAGATAC | 55833 |
rs569372432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980377 | AGCTGGGACTACAGG[A/C]GCCCGCCACCACACC | 55833 |
rs569410717 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012485 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTAC | 55833 |
rs569419028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985582 | AGAAAGATAAATATC[A/G]CACGTACTCACTCAT | 55833 |
rs569426015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932935 | CTTGACAATCCCATT[C/T]AATCTGTGAACGAGG | 55833 |
rs569426585 | snp | A/T | 3.29473e-05 | 0.00405864 | missense | UBAP2 | GRCh38.p7 | 9:33923836 | CACTGGGCATGCCTG[A/T]GTAGTAGGGAAGACC | 55833 |
rs569448262 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017686 | AATCCCAGCAATTCA[C/G/T]GAGGCCGAGGCAGGC | 55833 |
rs569455350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973334 | TACCCAGACAATATT[A/C]TCATTATTCCTAGTA | 55833 |
rs569463467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929398 | GGAGTACATCAACCT[A/G]CTGAATTAAAAAGTC | 55833 |
rs569468313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020620 | CGTGTGCCACTGAGC[C/T]GGCCCAGAGCCAACG | 55833 |
rs569470328 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025225 | TAGGAATGCTTCTAC[A/G]ACAAGTACCCAGTTG | 55833 |
rs569500583 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925045 | TATGGCAGATACAAC[A/C]AAGTGTGGAGACAGA | 55833 |
rs569543050 | snp | C/G | 0.000214406 | 0.0103517 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933568 | AGTGCAGTGCAGGAG[C/G]TGGTGCTGGGCAGGG | 55833 |
rs569597262 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927565 | CAACTCGGCTCCAGG[A/G]AAGAACAAAGAGGAA | 55833 |
rs569602198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014049 | TTAAAAGGGCCAGGT[A/G]CAGTGGCTCACACCT | 55833 |
rs569604816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962590 | GGCGGAGGTTGCAGT[G/T]AGCTGAGATCATGCC | 55833 |
rs569622149 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033521 | TGAGTACAAAAATAA[C/T]AAGACCCACTATTTG | 55833 |
rs569647928 | snp | A/G | 0.000137268 | 0.00828344 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989141 | TCTATCAGAGAGAAC[A/G]GCTGTTAATCATTTA | 55833 |
rs569665428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940977 | TCTCCAAGGTATGCC[C/T]GTAGTGTCATCCATA | 55833 |
rs569682213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948252 | AACTGAGAAACTGCA[A/G]GAGTTCTACTAAAAA | 55833 |
rs569692461 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926056 | GCAACCCTGGTCTCA[A/G]AGTAAGGCTGCAACC | 55833 |
rs569723224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983527 | ATGATATTTTAACCA[C/G]AACAGGGTGGTAAGG | 55833 |
rs569751320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949740 | ACGCGCACACACGCA[C/G]AAGATCAAATACAGG | 55833 |
rs569779218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927268 | GCCCGGCCACCACAC[C/T]GAGGTTGTTTCAACG | 55833 |
rs569799213 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958594 | TGTATTTTTAGTAGA[C/G]ACACGGTTTCACCAC | 55833 |
rs569801751 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026690 | TTTATATGTACAGTA[G/T]TAAGTCACTAATCTT | 55833 |
rs569807570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048535 | GGCAGAAACCCGAAA[A/G]GGGGGAGGGGAGGCA | 55833 |
rs569809154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989516 | CATGCACGTATCTTT[C/T]AAACCTAACTACCCA | 55833 |
rs569820720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927644 | AATTCATCCCCATCA[C/G]GGGTGGGGAGATTGG | 55833 |
rs569829035 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924718 | GGGGGACAGGGGGCA[C/G]TGCCAGGTAGGCACG | 55833 |
rs569834387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005694 | GATAAATAGGAATGG[C/G]AGAAAAGAAAGCAAA | 55833 |
rs569840918 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024267 | GAATCGCTTGAACCC[A/G]GGAGGAAGAGGTTGC | 55833 |
rs569846454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016211 | AGGAAGAGGAGGAAT[A/G]GGAGGAAGAGGAGGA | 55833 |
rs569849102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977497 | TTATCTGGAATGAAC[A/G]GATTAATCTAGCAGC | 55833 |
rs569850860 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008538 | CACCTGAGGTCAGGA[C/G]TTCCAGACCAGCCTG | 55833 |
rs569871406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009689 | GGTCTCGAACTCCTG[A/G]ACTCAAGCAATCCTC | 55833 |
rs569936597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009005 | TAACATTTAGGATAG[C/T]GGGGTGAATATATCT | 55833 |
rs569939269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925645 | GGGAGAAGCCGCTCC[A/G]CTCCCAGGCTAGGCC | 55833 |
rs569963114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970833 | TTTGAGATGAAGTCT[C/T]GCTCTGTTGCCCAGG | 55833 |
rs569963532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022332 | GCATCCAAGCTGGGC[A/G]AGGTGGCATGCACCT | 55833 |
rs569965989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975502 | TTGTGCACTGCTGGT[A/G]AAAACGTAAAATGGG | 55833 |
rs569972324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034656 | CAGGCGGGCGGATCA[A/G]GAGGTCAGGAGATCA | 55833 |
rs569988099 | in-del | -/A/CA | 0.161267 | 0.233723 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041298 | CTCTACTAAAAATGC[-/A/CA]AAAAAAAAAAAAAAA | 55833 |
rs570032734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040446 | ACAGATATGAATGGT[C/G]TCCATGCTCTAGTTA | 55833 |
rs570057620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932247 | AATCTCTGCGTCTGA[A/G]TCAGGAAAGAAGGCA | 55833 |
rs570074637 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955050 | TCCCATAAGTTCCTT[C/G]CTTTTCTGTAATCTA | 55833 |
rs570109081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002884 | GTACAAACAAGGTTC[C/T]GCCATGTTGCCCAGA | 55833 |
rs570122800 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982445 | AAAAATAGGTAGGTA[A/G]TTTGCCTACATAGCT | 55833 |
rs570125064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954669 | TTCCTCTCCCTTATA[G/T]ACTATAGCCAAGTTG | 55833 |
rs570160164 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968781 | CATCACCTCTAATTC[G/T]AGAACATTTTCATCA | 55833 |
rs570166526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976037 | CCTGGGCAACAAAGC[A/G]AGATGCCACCTCTAC | 55833 |
rs570190774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968499 | TGAGCACTAATGGGA[C/T]GCGGTACAAAGTCTC | 55833 |
rs570235049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961369 | AATAAAATATTAGCT[C/T]TACTACATGGCTTCC | 55833 |
rs570240692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947275 | TCTCTCTATATGCCC[C/T]AACCATAAACCAGCC | 55833 |
rs570257072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995989 | TTTTTGGAAACTGTA[A/C]GGCTGGAGTAGATCA | 55833 |
rs570274301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960649 | GCCAGGCATGGTGGC[A/G]CACATCTGTAATCCC | 55833 |
rs570278194 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955571 | TGGTGGCTCACATCT[A/G]TAATCCCAGCACTTT | 55833 |
rs570286767 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040982 | AACCAAAAATTCCAC[A/T]CTCAGTTATGTAGTC | 55833 |
rs570317153 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955449 | ACTTGAACTCAGGAC[A/G]GCGGGGGTTGCAGTG | 55833 |
rs570345106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047401 | AAACTATCATCTCCA[A/G]GGAGTGGAATACATT | 55833 |
rs570373258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003645 | CTCCTGACCTTAAAT[A/G]ACCCTCCTGCCTTGC | 55833 |
rs570399547 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027460 | AGTGGCTCATGCCTG[A/T]AACTCCAACAGTCTG | 55833 |
rs570425103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028850 | TAAAGCAGGGATCCC[C/T]AATCCCCAACTCCCA | 55833 |
rs570472557 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954581 | CTGACATTCTCACCA[A/C/T]GCCAATAAGACAGGC | 55833 |
rs570488450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935416 | TTACAGGCACGCGCC[A/G]CCACCACACCCGGCT | 55833 |
rs570491262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035278 | GAGGCCGAGGCGGGC[A/G]GATCACCTGAGGTCA | 55833 |
rs570504752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021719 | GCTCACTGCAACCTC[C/T]GTCTCCCGGGTTCAG | 55833 |
rs570514925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027673 | CCATCCTGGCTAACA[C/T]GGCGAAACCCCATCT | 55833 |
rs570522395 | snp | A/G | 6.59065e-05 | 0.00574012 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989021 | GGTTGTTGTTTCCAC[A/G]TCCACGACTCGATTC | 55833 |
rs570546311 | snp | A/C | 0.000132273 | 0.00813136 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926697 | AGTGTATTTTAGGAA[A/C]CACATACCACACCCT | 55833 |
rs570551484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958028 | CATGATCACTGAGGC[G/T]CACTGCAGCTACAAA | 55833 |
rs570561728 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956559 | ATCTCCAATTCCTGG[A/C]CTCAAGTGATGCACC | 55833 |
rs570584072 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932844 | GAAAACTCCAGAGCC[A/G]GCTTCCCTCAACGAC | 55833 |
rs570591987 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997205 | GATGAAAGAAACTCT[A/T]CAGTTTATTCTCATT | 55833 |
rs570628889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029458 | TGCTTGAACCCAGGA[A/G]GCGGAGGTTGCAATG | 55833 |
rs570633229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925271 | CATAGCAGCCTAGAA[C/T]CCCCGGAAGAGGCAG | 55833 |
rs570640054 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029744 | CCTGTAAACCCAGCA[C/T]TTTGGGAGGCCAAGG | 55833 |
rs570641320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022269 | AAAATAAAAAAATCA[C/T]CTTCAGCACTAATAC | 55833 |
rs570649064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982996 | GCAATTCTCTGCCCC[A/G]GCCTCCAAGTAGCTG | 55833 |
rs570650231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023773 | AATACAGGCCGGGTG[C/T]AGTAGCTCACGCCTG | 55833 |
rs570651178 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979665 | AGGCGGGCAGATCAT[C/G]AGGTCAAGAGATTGA | 55833 |
rs570669734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023141 | TGAGGCAGAAGAATC[A/G]CTTGAACCCAGGAGG | 55833 |
rs570674613 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034179 | TATAAAAGTTCAACA[A/T]ACCTATTAAGTCATT | 55833 |
rs570713100 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930857 | GCTGAGATTGCGCCA[C/T]TGCACTCCAGCCTAG | 55833 |
rs570724332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005852 | CAAAAAATGCATAAA[C/T]ATGTCAATGAAAATA | 55833 |
rs570742555 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925615 | CAGATTAAAGGGCTG[C/T]TGGTTTGCACAGTGG | 55833 |
rs570772551 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039744 | CTAGGAAAACCAGAG[A/T]CCCTTGTTCACTTGT | 55833 |
rs570788147 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:34017134 | ACAATGGTCACTGCT[C/T]ACTGAAGTCATCATA | 55833 |
rs570800998 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023775 | TACAGGCCGGGTGCA[A/G]TAGCTCACGCCTGTA | 55833 |
rs570802705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937561 | GCAGTGAGCCAAGAT[C/T]GCACCACTGCACTGG | 55833 |
rs570833922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046266 | CCACAAAGTGTCTTA[C/T]TAACAAAGGAAATCT | 55833 |
rs570870306 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981405 | AATATCTGAAGGCTG[C/G]AGTGTAGTGGCACAA | 55833 |
rs570889752 | in-del | -/TGTTTTCAT | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923594 | ACCACAGGGGACCTG[-/TGTTTTCAT]TAGTGCAACACATGC | 55833 |
rs570890003 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947073 | CCTTCTAGGAATCTG[G/T]AATTTTGCTATGTGC | 55833 |
rs570927733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959997 | GGCTAGAGGGCGGTC[A/G]AATGATAATGCAGCC | 55833 |
rs570951635 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971120 | ATTATGTTTCTATAA[A/G]TATAATCTCAATAAT | 55833 |
rs570958778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981605 | GTGATCCTCTCACCT[C/T]AGCCTCCCAAAGTGC | 55833 |
rs570974392 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959008 | ACAAACATTGGCCAG[G/T]CATGGTGGCGTGCAT | 55833 |
rs570993887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974923 | AGCCTGGTTAACAGC[A/G]TGAGACTAAAAAAAA | 55833 |
rs571014698 | snp | A/G | 1.733e-05 | 0.00294358 | stop-gained | UBAP2 | GRCh38.p7 | 9:33922551 | CAGGTTTGGAGGCTT[A/G]AGACTTGGGCTGCAG | 55833 |
rs571025660 | in-del | -/GAGGAG | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016162 | CAAGGTGAAAGGGGA[-/GAGGAG]GAGGAGGAGGAGGAA | 55833 |
rs571044047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019140 | GTGCAGTGGCTCACA[C/T]CTGTAATCCCAGTAC | 55833 |
rs571080516 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045238 | GTAGTCCCAGGTACT[C/T]GGGAGGCTGAGGCAG | 55833 |
rs571107903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960618 | TCGTCTCTACTAAAA[A/C]AAAAATACAAAATTA | 55833 |
rs571128928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012674 | AGTGAAGAAGAACCT[C/T]ATTCACAACTACTTG | 55833 |
rs571152989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025554 | CATTTTTAACTTCTT[C/T]AGAAACAAAATCAGC | 55833 |
rs571154955 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977437 | ACCTGGTAGTAACGC[C/T]ACTAGTAACATTGGT | 55833 |
rs571164984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008943 | GCACTCCAGCCTGGC[A/G]ACACAGCGAGACTGT | 55833 |
rs571167450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037611 | ATAAATTAGCAATTT[A/C]CTTAGCATTGATGAA | 55833 |
rs571230303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043472 | ACACCCAAACTATGC[C/T]GTATTTTTCAATAAA | 55833 |
rs571245190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002532 | ACAGGTGCATGCCAC[C/T]ACGCCTGGCTAATTT | 55833 |
rs571250315 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006699 | AAAAAAAAAGATAAC[A/G]TAAAGAAAATGTGGG | 55833 |
rs571276181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962449 | TCAGGAGTTCAAGAC[A/C]AGCCTGGTCAATATG | 55833 |
rs571292990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934560 | CTTGTTCATAGATAA[A/G]CTGTATAAAGACACC | 55833 |
rs571349327 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921961 | TTGGGTGGAGGGATA[C/T]CGCTGCTATTCCCAG | 55833 |
rs571378477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005493 | ATCTCTAAGTTTTTC[C/T]ATTTCTTCTTTAAAT | 55833 |
rs571388221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997618 | TCATTTTTATCAATG[A/T]TCTGTACTAAGTGAA | 55833 |
rs571393212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957334 | AGGCCCCCATGAAAC[C/T]ATCACCACAATTAGG | 55833 |
rs571414286 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957876 | CAATATAAAAGTGCT[A/C]AATTGTTTACCGGTT | 55833 |
rs571420414 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047309 | ACTAATCACTTCTGC[C/T]TAATGATAAGAGAAG | 55833 |
rs571479280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964483 | CTGCTTCAACACTTG[C/T]ACAACATTCGGCTTC | 55833 |
rs571479880 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037517 | ATCAGTGTTTCAAAA[C/G]TTAGGGTTGGCATAG | 55833 |
rs571493387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34006101 | AGCCGGGCATGGTGG[C/T]GTGCACCTGTAATCC | 55833 |
rs571507369 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014544 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 55833 |
rs571521857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955511 | GGCGACAGAGTGAGA[A/C]TCCGTCTCAAAAAAA | 55833 |
rs571534587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991585 | CTGAAGGAAGAGGTA[C/T]AAGTCATTATTTAAG | 55833 |
rs571561534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33999086 | CCTTTGACCAAACGA[C/T]CTAAAGCTATTGTTC | 55833 |
rs571569133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010017 | TCTCCATCTTGGTCA[A/G]GCTGGTCTCAAACTC | 55833 |
rs571634085 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028933 | ACCTGGGCGGCGTGG[C/T]AAGTCCTCGTCTATA | 55833 |
rs571653251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990820 | TTTTGTAATTTTAGT[A/G]GAGACGGGGTTTCAC | 55833 |
rs571663885 | snp | A/C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921361 | TTTGCTTCAGATTGT[A/C/T]AAAGTCCACTGAGAT | 55833 |
rs571665324 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927337 | CCCCAGTCCCTAAGG[A/T]CCCACTGCACTGAGC | 55833 |
rs571686069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017687 | ATCCCAGCAATTCAC[A/G]AGGCCGAGGCAGGCA | 55833 |
rs571696346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047739 | AATCCCAGATACTCA[A/G]GAGGCTGAGGTGAAA | 55833 |
rs571697785 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955841 | TCAAAATAGAAAAAA[A/T]AAAAAAAAAAGTTTA | 55833 |
rs571727892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048388 | GCATAAGTTGGGGCT[A/G]TAACAGGGCCAGTCC | 55833 |
rs571736163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030193 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 55833 |
rs571792388 | in-del | -/AATA | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966949 | GGACCACCGTGAATT[-/AATA]AATTCAAAGACTGAG | 55833 |
rs571857421 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036573 | ACATTTAAACTGTGT[G/T]TGTCTGCTCACCAAC | 55833 |
rs571866485 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942818 | ATGACTGCTGCAAAC[-/AT]GTGGAGAAATTAGAT | 55833 |
rs571879244 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948821 | TTAAAGGGAAGGGAA[A/C]TATTTGCCATGAATT | 55833 |
rs571916039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949146 | CACTACAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 55833 |
rs571916941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33955637 | AATTCGAGACCAGCC[C/T]GACCAACATGGAAAA | 55833 |
rs571922360 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976834 | AATCCCATCTCTACT[-/A]AAAAAAAATGTATAT | 55833 |
rs571950684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016823 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 55833 |
rs571967005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969492 | GGTTCAAGGCTACAG[C/T]GAGCTATGATCACAC | 55833 |
rs571988396 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023452 | CTCACTTGTCAAGGA[A/G]GAAAACCATAACTCT | 55833 |
rs572001009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017348 | TTTGCTGGTATCTGT[C/T]AAACCAATTCGACTA | 55833 |
rs572040796 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959080 | CTTGAACCCAGAGGC[A/G]GAGGCTGCAGTGAGC | 55833 |
rs572049659 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021864 | GTTTCGAACTCCAGA[C/T]CTCGGGTGATCCAAC | 55833 |
rs572060083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002531 | TACAGGTGCATGCCA[C/T]CACGCCTGGCTAATT | 55833 |
rs572103610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962157 | TTCCAGGAGAAAAAC[A/C]ATGATGAAACATTAC | 55833 |
rs572135528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010326 | CTACTCAGGAGGCTG[A/G]GGTGGGAAAATCACT | 55833 |
rs572139626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970290 | CATAAGAAGCTTAAC[A/G]ATTTTACTAGTGTTT | 55833 |
rs572160709 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010894 | GCAGATATGTCAGAG[C/T]AGAAGATAAACCAAA | 55833 |
rs572165745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993760 | AACAAGTGTATTCTT[C/T]CACAACTATATTCAG | 55833 |
rs572183234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041428 | CAAGATCGCACCATT[A/G]CACTCTAGCCTGGGC | 55833 |
rs572189269 | in-del | -/AA | 0.320814 | 0.239761 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010123 | GAGGTCCTGTCTATT[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs572224771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33997015 | TCTAGCACAGGAGAC[A/G]GAGCGAGACCCTGTC | 55833 |
rs572255172 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036336 | TGGTCAGGATGGTCT[C/T]AAACTCCCGACCTCA | 55833 |
rs572280320 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028990 | GCTTGGTGGCGCACA[A/C]CTGGAATCCCACCCA | 55833 |
rs572286683 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003839 | ATTCTAGTGTCTCAG[C/G]CTCTTGAGTAGCTGG | 55833 |
rs572418367 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941927 | TCATAAAAAAAAAAA[-/AA]CATAAACAGCTTCAC | 55833 |
rs572444796 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974449 | GAAGTTGAGGCTGCA[A/G]TGAGCTGAGATTGCA | 55833 |
rs572455348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040565 | AGCCCAGCCAACATA[A/G]CGATACACTCTAATT | 55833 |
rs572458918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995226 | GCTGGTCGTGGTGGC[A/G]CATGCCTGTAGTACT | 55833 |
rs572461005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039944 | CGGGCGATCACCTGA[A/G]GTCGGGAGTTCAAGA | 55833 |
rs572476013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996047 | CTACGACTTCATGAA[G/T]AAACCATACATAACA | 55833 |
rs572508482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950097 | TTTTGAGACAGTCTC[G/T]CTCTGTCACCCAGGC | 55833 |
rs572511991 | in-del | -/A | 0.0865458 | 0.189163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972649 | GAAGCAACAAAAAGT[-/A]AAAAAAACACCCAGA | 55833 |
rs572559211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028214 | ATGAGTGCTGGTGAA[C/T]TCAAACACTATAGGA | 55833 |
rs572559351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938822 | AAAAAAAGCTTGTCA[C/T]TGAAATTTCCATAGT | 55833 |
rs572563586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954799 | CTATAAGACATAATC[A/G]TTAATCATTTTTATT | 55833 |
rs572567907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949039 | GGGAGTTTTGGCAGG[C/T]GCTTGTAGTCCCAGC | 55833 |
rs572571312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939604 | CTCTACAAAAAAATT[A/G]GCCAGGTATGGTGGC | 55833 |
rs572574543 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992651 | ACAAAGACAACTTAT[A/C]GGGCGGAGGGGGGGG | 55833 |
rs572603174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954195 | TACAGGCGTGAGCCA[A/C]CCTACCTGGCCAAGT | 55833 |
rs572663044 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000910 | ATACCCAAAAAGACA[C/T]TGGTACAGAAATTCA | 55833 |
rs572686693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026672 | AGACACCATTCTAAG[C/T]ACTTTATATGTACAG | 55833 |
rs572723855 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015595 | GCCTCCCAAAGTGCT[G/T]GAATTACAGGCATGA | 55833 |
rs572738384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983130 | TGATCTGCTCGCCTC[A/G]GCCTCCAAAAGTGCT | 55833 |
rs572740312 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928078 | GGCGCTTGGGCCCAA[A/G]TCTCAAGGCTGAGCA | 55833 |
rs572765668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005746 | CAAAAGACAACCCAA[C/T]TTAAAGCTATGGACA | 55833 |
rs572865949 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985133 | ATACAAAGAAAAGGA[A/C]ACCAATAGTGCTTCA | 55833 |
rs572894108 | in-del | -/ACAGAGTGAG | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984658 | ACTCCAGCCTGGGCA[-/ACAGAGTGAG]ACACTGTCTCTTAAG | 55833 |
rs572902454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991981 | TACCCTGGCCAGGCA[C/T]GGTGGCTCACACCTG | 55833 |
rs572906795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936223 | CCTGGGCTCAAGCAA[G/T]CCTCCTGCCTTGGCC | 55833 |
rs572911881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043880 | CAACTGTAATCTCAG[C/T]ACTTTGGGAGGCCGA | 55833 |
rs572919322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037776 | CAATATGTAAATACA[C/G]AAACCCTGACTGGAT | 55833 |
rs572936004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985872 | AGCAAAAATACAAAA[A/C]TTAGCTGGGCATGGT | 55833 |
rs572963471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978632 | AAAAATACAAAAAAT[C/T]AGCCCGATGTGCTGG | 55833 |
rs572998791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044402 | CAAGACTCTGTCTCG[A/G]AAAAAAAAAAAAATT | 55833 |
rs573015157 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935165 | CTGTTGGAAGTGGCG[-/GG]GGGGGGGGGTCTCAT | 55833 |
rs573029167 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972028 | CATCCTAAAGCAGAC[A/G]AGGAGACGTATAATC | 55833 |
rs573036243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935570 | CCCCGCCTGGCCCAA[A/G]CATCTTTAAAATGCA | 55833 |
rs573050014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977963 | GAGGTTGCAGTGAGC[C/T]AAGATCGCACCACTG | 55833 |
rs573054719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980523 | TGGGATTACAGGCGT[A/G]AGCCACCGCACCCGG | 55833 |
rs573122795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941997 | GACCCACCTAATTTA[A/C]CTGAGAGATAGGGGG | 55833 |
rs573125114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971882 | GTAAAAGACATCACC[A/T]CTCCTTCCCCTATTT | 55833 |
rs573141116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991015 | CGTGGCCGAGCACAC[C/T]GGCTCACGCCTGTAA | 55833 |
rs573160773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934118 | TAAGGCAGATTGGGG[C/T]TGATGCCTATGTTGT | 55833 |
rs573176745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983905 | TTACCTAGAATAATA[C/T]TGAATCCCTGGGATT | 55833 |
rs573194309 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964378 | CAAGAAATCTGCTAC[A/T]TTAAATAATAAGTGG | 55833 |
rs573197253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941389 | TGTAGAAGTACCCAG[C/T]ACTACAGCCAAAGTG | 55833 |
rs573231236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005092 | ACATGGTGAAACCCC[A/G]TCTACACTAAAAATA | 55833 |
rs573233438 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942534 | AGAGTTTGAGGCCAG[G/T]CTGGGCAACATGACG | 55833 |
rs573238775 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018312 | AAATTCTAAAAGAGC[C/T]GTAACACTATAATTG | 55833 |
rs573252803 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024538 | TATTAAAGATGTCCA[A/G]CAAAAAAATTTCCAG | 55833 |
rs573301069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005038 | GAGGCTGAGGCAGGC[A/G]GATCACTTGAGGTCA | 55833 |
rs573313167 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011982 | ATTATTTATGCCCAC[A/C]ACCAAAGATAAACAT | 55833 |
rs573324310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963309 | ACATTAAATACAGAA[A/G]GCAAAGGCTCAGGTC | 55833 |
rs573338856 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024987 | AGACTCTGTCTCCCC[A/C]AAAAAAAAAAACTTC | 55833 |
rs573439492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005679 | AAAGAGAAATGAAGA[C/G]ATAAATAGGAATGGG | 55833 |
rs573466865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019339 | ACCCAAGAGGCGGAG[G/T]TTGCAGTGAGCCAAG | 55833 |
rs573475531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957015 | GAATCGCTTCAGTCC[A/G]GAGGTTGAGGCTGCC | 55833 |
rs573483172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990980 | AATTCTACTTCTAGG[C/T]CCTTATTCAAATAAA | 55833 |
rs573513944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964031 | ACGCCCATGTTTACC[A/G]AGCTCCCTTCTCACT | 55833 |
rs573565200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34031934 | TTGAGCCCAGGAGTT[C/T]GAGACCAGCCTGGGT | 55833 |
rs573566771 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050036 | GGCTGATCTGGCTGT[C/G]TAGGCGGGTGGCCCC | 55833 |
rs573579249 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049277 | CACTCAGGGCAAGCC[C/T]GGCCTCCCAAATGTT | 55833 |
rs573585507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935428 | GCCGCCACCACACCC[A/G]GCTAGTTTTTCGTAT | 55833 |
rs573598397 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923232 | TGGTGCCTGCGATGA[C/T]CCAGCATAGCCACCT | 55833 |
rs573610022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34043611 | CAATCCTCCCACCTC[A/T]GCCTCACAAGTAGAT | 55833 |
rs573630715 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939861 | AGGAGGGGGAGGGGG[-/A]GGAGGAGGAGGAGGG | 55833 |
rs573661036 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960546 | TTTGGGAGGTTGAGG[C/T]GGGTGTATCACCTGA | 55833 |
rs573687827 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989423 | AGCCATGATGGTCTC[C/G]ATCTCCTGACCTCGT | 55833 |
rs573700457 | in-del | -/T | 0.326506 | 0.238006 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981522 | ATCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTAA | 55833 |
rs573719880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942813 | GGAAAATGACTGCTG[A/C]AAACATGTGGAGAAA | 55833 |
rs573751699 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039996 | AACCCCGACTCTACT[A/G]AAAGTACAAAATTAG | 55833 |
rs573756545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950901 | ACAATACACACATGT[A/G]CATACATGCACATAC | 55833 |
rs573761661 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976074 | TTTTTTTAATAAATG[-/T]TTTTTTAAGAAGGCA | 55833 |
rs573761682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983830 | AGCAGTTTCAGCTTG[G/T]GGAAGACAGAATTAT | 55833 |
rs573767865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957396 | TTCCACCTGTCCCTG[G/T]GGAATCACTCAATCC | 55833 |
rs573782446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942093 | CAGAGGTGGGCGGAT[C/G]CGGAGGTCAGGAGAT | 55833 |
rs573795127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34037697 | CTGGCAATTATATCT[C/G]ATAAATAATTGAGAA | 55833 |
rs573799631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983365 | GTCATGAAGATTTGA[A/C]GATTTCTCTAAGACG | 55833 |
rs573841315 | in-del | -/TG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925825 | AGCAACAGGAAAGAC[-/TG]TATCCAGCAGAGGTG | 55833 |
rs573848115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025911 | CAAGGACCTTTCTGA[A/C]GATAAGATACCTCAG | 55833 |
rs573914279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949268 | AAAACTAAAGAGGAA[C/T]GCCATGAAATACATG | 55833 |
rs573947022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979283 | CTTGACTCAATCTCA[A/C]CAAAAGACCAAAATA | 55833 |
rs573947100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985792 | TTTGGGAGGATTAGG[C/G]AGGTGGATCACTTGA | 55833 |
rs573980784 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966280 | TGGTGAAACCCTGTC[C/G/T]CTACTAAAACTACAA | 55833 |
rs573994426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041970 | GTGAATGTTGCAGTG[A/G]GCCAGGATCGAGCCA | 55833 |
rs574021855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011082 | AACCAAAGAAACACC[A/G]ACCCGATTAAAATAT | 55833 |
rs574037372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941305 | TGATGAAGAAGCAAA[A/T]ACATTCAAAGCAAAT | 55833 |
rs574063000 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036314 | TAGAGATGGGGTTTC[A/T]CCATGTTGGTCAGGA | 55833 |
rs574126298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924834 | GCTTGTCCAACCCAC[A/G]GCCCATGACAGCTTT | 55833 |
rs574148473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34030216 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACGGGG | 55833 |
rs574159886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981236 | TTCTGGATATATATA[C/T]ATATTCTGGATATAT | 55833 |
rs574167746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017983 | TTGAACAAACATTTA[C/T]TGACTAGCTACTAAG | 55833 |
rs574168884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933206 | GCTAGGCTCAGGCAC[C/T]CTCTGGAGGGTGAAG | 55833 |
rs574208226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971841 | GATCTTCCACCAAAC[A/C]AGCCCAGTGCCTTCT | 55833 |
rs574223444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018688 | CTAACACGGTGAAAC[C/T]CCGTCTCTACTAAAA | 55833 |
rs574240921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980628 | AAGTATATTGATATC[C/T]TTTTCTGCATAAAGC | 55833 |
rs574313012 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971174 | AATAACCAATATTTA[A/C]CCCAAGAATTTCAGA | 55833 |
rs574338817 | snp | C/T | 4.94197e-05 | 0.00497066 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986768 | AGCTTACCTCTACCC[C/T]GGGCTCGCTTGCCAC | 55833 |
rs574339595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33945229 | GATGGCTGGGCGCAG[A/T]GGCTCACGCCTGTAA | 55833 |
rs574339986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962928 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 55833 |
rs574361127 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993886 | TTCATGAAAAGTTCA[C/G]CTTTGCTTTCTTTTT | 55833 |
rs574399784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928427 | GCCACAGGAAGCCCA[A/G]CGTAAGTCTCAATCT | 55833 |
rs574415611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039126 | CGTCTCCGCCCGGCA[A/G]CCGGCCCGTCTGGGA | 55833 |
rs574430922 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975564 | AGCACTTTGGGAGGC[C/T]GAGACGGACGGATCA | 55833 |
rs574434313 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038519 | CCAGCTGCTAACCGC[A/G]AGTGATCTGCCAGCC | 55833 |
rs574552622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027730 | GCCGGGGGTGGTGGC[A/G]GGTACCTGTAGCCCC | 55833 |
rs574566548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930473 | CAACAACAACAACAA[A/C]AAAAAACCCTTAAGT | 55833 |
rs574600388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959688 | ACATGCTCAAAAATA[C/T]CTGTGCAATAAAGGA | 55833 |
rs574646523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925342 | AGAGAAAGCCCAGAA[C/G]GGGGAGCACTTTCAC | 55833 |
rs574683988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967958 | CACTACATATTTCTT[C/T]ACTGCTGCTCTTCAT | 55833 |
rs574700922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34015442 | TCCCTGCCTCAGCCT[C/G]CCGACTAACTGCCAT | 55833 |
rs574730451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020163 | ATTAAAAAAAAAAAA[A/C]AAAAAAAACTAAGAG | 55833 |
rs574733996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931046 | ACTTTTCATTGTCTA[C/T]CTTTCCATAACTTTT | 55833 |
rs574777678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019596 | GAAGATGGACGGCAG[C/T]GGTGGTTGCACGACA | 55833 |
rs574784839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952616 | AACTTTCGCATTTAA[C/T]TGGAAAACAAGAAAT | 55833 |
rs574795620 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965929 | TGGCGGGTGCCTGTA[C/G]TCCCAGGCACTTGGG | 55833 |
rs574810072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925783 | GGAAGAAGGCATCAC[C/T]GCACAAGGGAGAAAG | 55833 |
rs574823496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958606 | AGAGACACGGTTTCA[A/C]CACGTTGGCCAGGCT | 55833 |
rs574825348 | in-del | -/T | 0.0998734 | 0.199905 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020325 | ATGCAGAGCCAATGA[-/T]TTTTTTTTTTTTTAA | 55833 |
rs574825706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936170 | GTATTTTCTGTAGAG[A/G]TGGGGTTTTGCCATG | 55833 |
rs574832486 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947118 | TAGGCACAGGGTACC[C/T]ACATTTCTTGCCCCA | 55833 |
rs574857807 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | UBAP2 | GRCh38.p7 | 9:33923919 | GTGTGGTGGGTCTGT[A/G]ATTGGCTCTGCTGTG | 55833 |
rs574861237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33979873 | CTCTGTCTCTAAATA[A/G]ATAAATAAGTGTAAC | 55833 |
rs574886480 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33992664 | ATCGGGCGGAGGGGG[C/G]GGGGCACAAATAGGG | 55833 |
rs574894834 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049176 | GCCCACAACTGCAGC[C/T]CGTCGTCGCGCCGTG | 55833 |
rs574927655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34000443 | GCCAGTCTGGTTTCT[C/T]AGTTTTAACGAAGGT | 55833 |
rs574991057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014078 | CTGTAATCCCAACAC[C/T]TTGGGAGATCAAGGG | 55833 |
rs575008105 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993272 | TGCCTTCATGCTCTT[C/G]CTCCTAGCAACATCA | 55833 |
rs575038283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007191 | TATTTGCTCTGGCTA[G/T]AAGTTCTAGTACTCA | 55833 |
rs575039949 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018271 | AGCCGGGAATTTTCC[A/G]ATAAAGACCAGAAAA | 55833 |
rs575119997 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034690 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTTT | 55833 |
rs575128538 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010125 | GGTCCTGTCTATTAA[-/A]AAAAAAAAAAAAAAA | 55833 |
rs575144177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951599 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 55833 |
rs575154458 | in-del | -/TTTTTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939206 | TTTTTTTTTTTTTTT[-/TTTTTC]TTTTTGAGATGGAGT | 55833 |
rs575180697 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017834 | TAGGAGGCCAAGGCA[G/T]GAGAATGGCGTGAAC | 55833 |
rs575194010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935411 | TGGGATTACAGGCAC[C/G]CGCCGCCACCACACC | 55833 |
rs575256863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34026851 | CACTTAACTATTATG[C/T]TATGTTGTAAGGCTA | 55833 |
rs575275658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934890 | CAGCCTTGGCAGCCC[A/C]ACAATACCAGCAAAT | 55833 |
rs575285961 | snp | C/G | 1.67978e-05 | 0.00289804 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943628 | CAGGAACAGAGGTCA[C/G]AGATTCCAGGTCACA | 55833 |
rs575294477 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009467 | GTCTCGCTACTTGGC[C/T]CAGGATGGTCTTGAA | 55833 |
rs575302314 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032952 | CAACATCTTTGCTTC[C/T]TGATACTCTAAGCCA | 55833 |
rs575324141 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33980555 | GAGCGTCATTTCTAA[C/T]ACATAAACACACTCA | 55833 |
rs575332719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021088 | TTTCTACATATTTTT[G/T]ATCTGTGTATCATAA | 55833 |
rs575343906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34038388 | AACCTCCCTGCCTGA[C/T]TCTCCTGCCTCGGCC | 55833 |
rs575367484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032678 | CCTGTAATTCCAGCA[C/T]TTTGGGAGGCCGAGG | 55833 |
rs575374333 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971929 | GCCAGCCATGGAGAT[C/G]CAGATGTGAAAACCA | 55833 |
rs575387852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936328 | GAGATGGTGTCTTGC[A/G]CTGTCACCCAGGCTG | 55833 |
rs575425997 | in-del | -/GCAAAAAATGTAG | 0.00318978 | 0.0398085 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947093 | TTGCTATGTGCTATA[-/GCAAAAAATGTAG]GCACAGGGTACCTAC | 55833 |
rs575431622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34032007 | AAAATTAGCCAGGTA[C/T]GGTGGCGCATGCCTG | 55833 |
rs575434400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929775 | GGGAGGCCGAGGCAG[A/G]TGGATCACCTGAGAT | 55833 |
rs575455412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964717 | CCCCCATCTCTTAAA[A/G]AAAAAAGAAGCAAGA | 55833 |
rs575459539 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962556 | GAGGCTGAGGCAGGA[A/G]AATCGTTTGAACCCA | 55833 |
rs575463604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930305 | GCTGTTCCACATCAC[A/G]TACTGACCCGCTACA | 55833 |
rs575469459 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021775 | AGCAGCTGGGACTAC[A/T]GACGCCTGCCACCAC | 55833 |
rs575491557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974335 | CAAATGGCAAAACCT[C/T]GTCTCTACAAAAAAT | 55833 |
rs575529719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957850 | AGACAGTAGGTGTTC[A/G]TTTTCTTCAACAATA | 55833 |
rs575531346 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988308 | AATATCAGTGGAATA[C/T]ATGAGACAGCAAGAG | 55833 |
rs575546524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928543 | TGACACCTTTCAGTC[C/T]ACCAATGCCTCACCA | 55833 |
rs575574921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978681 | ACTATTCGGGAGGCT[A/G]AGGCAGGAGAATGGC | 55833 |
rs575663837 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928995 | GATTCACCAAGGTAA[A/T]GACAGCCAAAAACAT | 55833 |
rs575669320 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBAP2 | GRCh38.p7 | 9:33964963 | TAATAGGTGAATGGG[A/G]GTAACTCAATGTGGC | 55833 |
rs575670582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931932 | GAGGCTCCAGCCTCT[C/T]TTAAGTTTTCATTGC | 55833 |
rs575670601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33939568 | CTTGAGACTAGCCTG[A/G]GTAACATGATGAAAC | 55833 |
rs575670988 | in-del | -/CTATT | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956257 | CACTTCGCATAACAG[-/CTATT]CTAAAGAAAATGAAA | 55833 |
rs575681491 | in-del | -/GGTGGT | 0.454784 | 0.1434 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016371 | AGCGGCGGCAGCGGC[-/GGTGGT]GGTGGTGGTGGTGGT | 55833 |
rs575696322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34018789 | AATGGCGTGAACCCG[A/G]GAGGTGGAGCTTGCA | 55833 |
rs575728561 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989493 | GGCGTGAGCCACCGC[A/G]CCCGGCACATGCACG | 55833 |
rs575762912 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050121 | AAGGAGGAGCATCCC[C/G]CATAGAAGAGGACAA | 55833 |
rs575777120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34019398 | ACAGAGCAAAACTCT[A/C]GGGGCAAGGGGTAAA | 55833 |
rs575790278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34005845 | AACAAACCAAAAAAT[A/G]CATAAATATGTCAAT | 55833 |
rs575807761 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043990 | AAAATTATCAGAGCA[C/T]GGTGGCAGGCTAATC | 55833 |
rs575842814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34044529 | AAGGCACCACAGCAC[G/T]CCAGCCTGGGCGACA | 55833 |
rs575845639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960978 | CGGGGAAAAAAGATA[C/T]ATACGCCTCACTAGC | 55833 |
rs575862080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975047 | AGTATTGCTGATCAT[C/T]AGGGAAATCCAAATC | 55833 |
rs575892611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951011 | ATCACTTCTGTTGCT[A/G]CTGTTATTTACTAGG | 55833 |
rs575904011 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015735 | CCAAGGTCTCACTCT[A/G]TCACCCAGGCTGGAG | 55833 |
rs575917149 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047710 | AACTAGCTGAGCACC[A/G]TGGTGCACACTGTAA | 55833 |
rs575917706 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34012827 | TGCAACTTTTCCGTA[A/T]ATCTCACAATGTATT | 55833 |
rs575921303 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989219 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 55833 |
rs575923363 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33952069 | AAATACTAAGGAAAA[A/G]TTTAAATATTCAATT | 55833 |
rs575929430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975744 | GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATCACA | 55833 |
rs575939613 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999853 | TAGCTGGGATTACTA[C/T]GTATGTATGTATGTA | 55833 |
rs575958018 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962008 | AGATGTTTCAAAACC[A/C/G]AAAACATTTAATTCT | 55833 |
rs575988115 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987113 | CCTGGGCAACATACA[A/G]AAAAATACAAAAATT | 55833 |
rs576001353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022501 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCCCAGCAA | 55833 |
rs576026191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008065 | GCTTGAACCTGGGAG[A/G]CGAAGGTTGTAGTGA | 55833 |
rs576035317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34028942 | GCGTGGCAAGTCCTC[A/G]TCTATACAATAAATT | 55833 |
rs576038722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34014858 | ACCTAGCCTAAAACC[C/T]CCAAATTTTTCCATC | 55833 |
rs576039455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969283 | AACTAAGCTGGGCAT[A/G]GTGGCTCATGTCAAT | 55833 |
rs576070104 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046173 | GAGAACTTTACAATC[A/T]GTAAATGCCTGCAGA | 55833 |
rs576088880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982684 | CTGCAGAATTTATCT[A/T]GCATACTTGCGATTA | 55833 |
rs576102949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926768 | GGGCTCTAACACACC[C/T]GGGAATGGGATCTGG | 55833 |
rs576129457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976545 | GGAAGAATGAAAGAA[C/T]TGGTGAAATGATAAA | 55833 |
rs576171472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970201 | ATCTCCTAATATCTA[C/T]ATGATCCATATCAAT | 55833 |
rs576178854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016708 | TTACAGGCGCACACC[A/G]CCACGCCCAGCTAAT | 55833 |
rs576242703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041251 | GGAGGTCAGGAGTTC[A/G]AGACCAGCCTGCCCA | 55833 |
rs576260496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34039897 | CACACGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 55833 |
rs576266869 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025110 | AAAAATGACTGAGAC[A/G]TGGAAACTAGACCGT | 55833 |
rs576270575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033823 | TCACTGCAACCTCTG[C/T]CTCCCAGGTTCAAGC | 55833 |
rs576304526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938720 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 55833 |
rs576304990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34010195 | TTGGGAGGTCAAGGC[A/G]GGCAGATCACCTGAG | 55833 |
rs576306269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34047905 | TACTGGCAAACCATA[C/T]ACCTTCCTTGAATGT | 55833 |
rs576315518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017229 | CAAAACAATCATAGT[A/G]AAAGATAAGCATGTA | 55833 |
rs576315601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009456 | ATGGAGACAGGGTCT[C/T]GCTACTTGGCCCAGG | 55833 |
rs576384857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938598 | GGTCAGGAGTTCGAG[A/T]CCAGCCTGGGCAACA | 55833 |
rs576447852 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953408 | CTGTTGGGAAGTTTC[A/G]AAGGAGTTGGCTTCT | 55833 |
rs576471502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33937869 | AGAGGTTGCAGTGAG[C/T]CGGGACCGTGGCACT | 55833 |
rs576475046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046364 | TTTAGAAGTAAAGGC[G/T]TCATGCCGGGCGGGG | 55833 |
rs576478428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045670 | AGCCACAGTGCCCAG[C/T]CACAAAAGAAAATTT | 55833 |
rs576487652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975615 | CATCCTGGCTAACAC[A/G]GTGAAACCTCATCTC | 55833 |
rs576520387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33967779 | TTATTCAATATTATA[C/T]TTGTAAACTGGAGTA | 55833 |
rs576520478 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33958838 | GAGCTGGCCAACAGT[C/G]CAAGACCTAGTCTCT | 55833 |
rs576554521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946311 | TCTGCCTAATTTGGT[A/G]TTTTCTGCCATACCC | 55833 |
rs576569150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33995177 | GTCTGGCCAACATGG[A/C]GAAACCCCACCTCTA | 55833 |
rs576575348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975256 | CCAATATGGTGAAAC[C/T]CCGTCTTTATTAAAA | 55833 |
rs576588325 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994092 | GTAGACATGGGGTTT[C/T]GCCATGTTGACCAGG | 55833 |
rs576589093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954073 | CACCATGCCCAGCTA[A/G]TTTTTGTATTTTTAG | 55833 |
rs576600272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960076 | CTGAGACTACAGATG[A/C]ACAACCCCACACCCA | 55833 |
rs576637733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959492 | TGCTCAAACTCTGTG[A/T]CAGACAGATACCAAA | 55833 |
rs576653413 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953131 | TGCCCCAGCTCCCAA[A/T]GTGCTGGGATTACAG | 55833 |
rs576674363 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025650 | AGAAAGTCTCCGGCC[A/G]AATAAACCAACCTGA | 55833 |
rs576720511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931118 | ACAGGCTTGAAATGC[A/G]TGGGTCCACTTACAG | 55833 |
rs576756302 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007421 | GATCTCTTGAGCCTA[-/G]GGGGGGTCAAGGCTA | 55833 |
rs576756643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987807 | ATTAGGTTCAAAGCC[A/T]GGAAAGGCACAGAAT | 55833 |
rs576776635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988719 | AACCACATGGGAGGC[A/G]CTTATGAAACTACTC | 55833 |
rs576778279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982090 | CAGGCCCCACTCCTT[G/T]CAGTTGCTTTTTACA | 55833 |
rs576819833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034103 | TTCACATCTCTGCAG[A/G]AACCATTTCAACATT | 55833 |
rs576831023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34020850 | TATTTTTTTAGTAGA[A/G]ACGGGGTTTCACCGT | 55833 |
rs576855599 | snp | A/G | 3.29707e-05 | 0.00406008 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924161 | GCTCCTGGAGTTCGC[A/G]CTAGGCCGGCCCCGG | 55833 |
rs576891252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021868 | CGAACTCCAGACCTC[A/G]GGTGATCCAACCGCC | 55833 |
rs576915102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33981958 | TATGAAATGGAAAAC[A/T]TCTCTCTGCTTTTCT | 55833 |
rs576958328 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008746 | CTGAGGCAGGCGGAT[C/T]ACAAGGTCAAGAAAT | 55833 |
rs576983067 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UBAP2 | GRCh38.p7 | 9:34022468 | TTTAAGACACAGTCT[C/G]GCTTTGTTGCCCAGG | 55833 |
rs577043387 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969050 | TTCTATGTATATTCT[A/G]TATTTTGCTTATACA | 55833 |
rs577058509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045580 | GGTTTCACCATGTTG[A/G]TTAGGTTAGTCTCGA | 55833 |
rs577059241 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986447 | GTATTTTTAAAATAA[C/G]GTTTAAAAAACCCTA | 55833 |
rs577062236 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977592 | AAGCGAATAAACCAT[A/G]TTATGGTAAATGCTG | 55833 |
rs577063989 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003398 | TTTTTTTTTGAGACA[A/G]TCATGCTCTGCTGCT | 55833 |
rs577094182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34002568 | TTTTTAGTAGAGAAC[A/G]GGTTTCACAATGTTG | 55833 |
rs577098487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960278 | TCCAATCTCCCAATC[A/G]TCTTGACAATTGGTC | 55833 |
rs577101348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34009319 | GGCCAGGCTGGTCTC[A/G]AACCCCTGGCCTCAG | 55833 |
rs577108091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34016658 | CCTCCTGAGTTCAAG[C/T]GATTCTCCTGCCTTA | 55833 |
rs577109044 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33993647 | CTCTAGCCTGGGCAA[C/T]GGAGTGAGACCCTGT | 55833 |
rs577186897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966076 | AAATCAGGGAGTGTG[A/G]GTCTTAGAACTTTTT | 55833 |
rs577210863 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921848 | ATAACTCAGATTATT[A/T]TTTTTTTTTTCATGG | 55833 |
rs577213800 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046457 | GACCATCCCGGCTAA[C/G]ACAGTGAAACCCCAT | 55833 |
rs577225691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017862 | AACCCGGGAGGCAGA[A/G]GTTGCAGTCAGCCGA | 55833 |
rs577282615 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929035 | GGGCTCCAAGGCGTC[C/T]TGTTCCTTCAGCACA | 55833 |
rs577296639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34007323 | GTAACTTGGTGAGAC[A/G]CTGTCTCTTCAAAAA | 55833 |
rs577314060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042236 | TGTAATCCCAGCACT[C/T]TGGGAGCTCAGGTGG | 55833 |
rs577323565 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935290 | GAATAGTAAATTTTT[A/G]ATTTAGAAGTAGTTT | 55833 |
rs577341080 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936439 | GCTGGGATTACAGGC[A/G]CGCACCACTACACCA | 55833 |
rs577374995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33959180 | ATTAAAGTACTTATT[G/T]TTTACAAGGTAAAAT | 55833 |
rs577381854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941417 | GTGCTCATACTACAC[A/G]CATGCTTGGTTTTCT | 55833 |
rs577387110 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34008026 | TTATTTTAAAAGAGG[G/T]CCAGAGGCTGAGGCA | 55833 |
rs577428427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033655 | CAATCTCGGTTCCCT[A/G]CAACCTCTGCCTCCT | 55833 |
rs577434734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33987281 | GCCAAGTGTGGTGGC[A/G]CGCACCTATAGTCCC | 55833 |
rs577449184 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34042797 | TAATTTTACATATGG[G/T]GCCAGGCATTAAGCT | 55833 |
rs577449384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036345 | TGGTCTCAAACTCCC[A/G]ACCTCAGGTGATCTG | 55833 |
rs577468908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001881 | ATAAGCTTTACAAGT[C/T]AAACACAAGAAAAAT | 55833 |
rs577554759 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040101 | GAGGCGGAGGTTGCG[C/T]TGAGCCAAGATCACG | 55833 |
rs577559950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34011018 | GAATATTTAAACTTG[A/C]AAACTGCCTGAGAAC | 55833 |
rs577608004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996090 | TCAGGTAATCGTTCT[C/T]TCTGGAACTTAAAAC | 55833 |
rs577619019 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941799 | GCAGGAGGTAATGAC[A/G]GAAGTTGTATATGTG | 55833 |
rs577619620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33994001 | CCGGGTTCAAGCAAT[C/T]CTCCTGCCTCAGCCG | 55833 |
rs577643630 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035457 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 55833 |
rs577656695 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049126 | TGTATTGTACTCGGA[A/G]TCATCAGGAGAGTAT | 55833 |
rs577657727 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959906 | CACAGATAAGCTTAA[A/C]AAAAAAATCAATCCT | 55833 |
rs577672149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34048627 | CAACGTGAGGGGAAG[A/G]GGAAGGAGGGAGCCC | 55833 |
rs577700030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34004626 | TCTCTACTAAAAAAA[C/T]ACAAAAAATTAGCCG | 55833 |
rs577734734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33950054 | GTTCTTCATCAAAAA[C/T]AACATTTCTTTTCTT | 55833 |
rs577735570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962262 | CACAGCTCAGCCACT[A/G]TATGTACAGTTAATG | 55833 |
rs577739439 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924363 | CAGCACATGGAAGTG[A/G]TGACGCCACACTCCT | 55833 |
rs577740379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:34021557 | TGAATAAATGCATAC[A/G]AACACACTGTTTTAA | 55833 |
rs577758233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996811 | CTTCAAAGGCCAGCC[A/G]CAGTGGCTCACAACT | 55833 |
rs577847587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962760 | GATGAGTGGATCACC[G/T]GAGGTCAGGAGTTTC | 55833 |
rs577890008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024339 | AACAGCAAAACTCTG[C/T]CTCAAAAAAAAAAAA | 55833 |
rs577904734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33990575 | GGTATTATCATACAG[C/T]TCTGGTGAGCATGCA | 55833 |
rs577942223 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975413 | TCCAGCCTGGGTGAC[-/A]AGAGTGAGGCTCTAT | 55833 |
rs577959098 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025888 | CCGGTTTAACTGCTG[-/T]TTTTTTTCAAGGACC | 55833 |
rs577969623 | in-del | -/A/AA | 0.499101 | 0.0211879 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017018 | AAAGAAAAAAAAGGA[-/A/AA]AAAAAAAAAAAAGAG | 55833 |
rs577978357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33954926 | GTCTTTTATCTTTCC[A/G]GATCACTACACTTTG | 55833 |
rs577985139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34003190 | CAGGCATGCCACCAC[A/G]CCCTGCTAATTTTTG | 55833 |
rs578004067 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAP2 | GRCh38.p7 | 9:33991059 | GGAGGCCAAAGCAGG[A/C]AGATCACTTGAGGCC | 55833 |
rs578005445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34029151 | TTAACAGTTCCTAAA[G/T]AAATTAAACAGTTAT | 55833 |
rs578011659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982847 | AATCTCCAATTCACT[A/G]GTTATCCCCTATAAT | 55833 |
rs578015774 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBAP2 | GRCh38.p7 | 9:34035652 | ATCGTGCTACTGTAC[C/T]CCAACCTGGGATATA | 55833 |
rs578049764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33947674 | AAAAAAATACAAAAA[A/C]ATCAGCCAGGAGTGA | 55833 |
rs578057890 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994049 | GCAGGCGCCCACCAC[C/G]ACACCTGGCTAATTT | 55833 |
rs578087306 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999820 | GCTTAACCAATGCTC[C/T]TGCCTCAGCCTCCAG | 55833 |
rs578089062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933168 | TCCACCTCAGTGACA[C/T]GGGCCCAGCGATGCC | 55833 |
rs578089424 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972177 | ATGCTCCTTTACAGA[A/G]ACATTAGATAAAGAA | 55833 |
rs578111722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983227 | CTGATTTATGACATG[A/G]ATCAGCTTGTAATCC | 55833 |
rs578132562 | snp | A/G | 8.23608e-05 | 0.00641667 | missense | UBAP2 | GRCh38.p7 | 9:33948496 | AACTGGCCCAAACTC[A/G]GAGCTTTCAACTGGT | 55833 |
rs578152788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977775 | TCGAATGATTCTTGT[G/T]CCTCAGTCTCCCGAG | 55833 |
rs578182462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:34046522 | GGTGGTGGGTGCCTG[C/T]AGTGCCAGCTACTCG | 55833 |
rs578210416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927398 | CCAAAGAGGGCAAGG[A/C]AGCCATGCAGTGCCA | 55833 |
rs578228076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33977319 | TGGGATTACAGGCGT[C/G]AACCACCGCGCCCAG | 55833 |
rs578235286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2 | GRCh38.p7 | 9:33940600 | ACTGGGCAACATGGT[A/G]ATACCCCGTCTCTAA | 55833 |
rs578239987 | snp | A/G | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970345 | TTGACCCTCTTTACA[A/G]TTTCTCTATTTACAG | 55833 |
rs745324195 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024342 | AGCAAAACTCTGTCT[-/C]AAAAAAAAAAAAAAT | 55833 |
rs745340549 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931794 | CCTGCCTCCTCCATT[C/T]GTCTGCACCCTAATC | 55833 |
rs745347097 | snp | A/C | 5.66203e-05 | 0.00532043 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922456 | GTGCTCGTGTGTTCT[A/C]TCCTGCCCAGGATAA | 55833 |
rs745350616 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012468 | CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA | 55833 |
rs745360210 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997660 | TACAATTTTTAAGAC[A/G]CACAGTCAACATCAA | 55833 |
rs745366106 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33944385 | AAGCTGGGGGTATCC[A/G]CCGCTTAGCAAGTTT | 55833 |
rs745374345 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044235 | TGAAACCTTGTCTCT[A/G]CTAAAAATACAAAAA | 55833 |
rs745382512 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967581 | GGAAACAGTCATACA[C/T]ACGTATCTGAAATAA | 55833 |
rs745384596 | snp | C/T | 1.70165e-05 | 0.00291684 | splice-acceptor-variant | UBAP2 | GRCh38.p7 | 9:33932629 | TGGCTGGAGAGCGAA[C/T]TAGAAGACAAAACAG | 55833 |
rs745387923 | snp | A/C | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33944468 | GTGCTGGGAAGCTGC[A/C]AAAGCTTGTTCACAG | 55833 |
rs745414400 | in-del | -/TAAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018014 | TGTCAAGCACATAAT[-/TAAG]TATGTCATCAAAACA | 55833 |
rs745428316 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022101 | AATTCAAAAATTAGC[C/G]GGGCATGGTGGCGCA | 55833 |
rs745447785 | snp | A/T | 3.53126e-05 | 0.00420179 | missense | UBAP2 | GRCh38.p7 | 9:33922527 | TCCAGTATGGAGAGT[A/T]GCCGTAGGCAGGTTT | 55833 |
rs745449642 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33922607 | GAGCCACTCTGAGGA[A/T]GAGGAGAAGGGAAGG | 55833 |
rs745457988 | snp | C/T | 1.70075e-05 | 0.00291607 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933482 | TTGGGCCCACACCTT[C/T]CCCATACCTGCTAAG | 55833 |
rs745465978 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023961 | ACGCAGGAGAATCGC[C/T]TGAACCTGGGAGGCG | 55833 |
rs745472355 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977898 | TCAATCTCTGTAGTC[C/T]CAGCTTCTCGGGAGG | 55833 |
rs745482507 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983322 | TAAAAGTAAAGGATT[C/T]AACAGTGTAGTCAGT | 55833 |
rs745535590 | in-del | -/ACAGGC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958100 | TAAGTAGCTGGGACT[-/ACAGGC]ACAGGCACCTGCCAT | 55833 |
rs745540110 | in-del | -/TTC | 1.84143e-05 | 0.00303428 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944687 | AATGGCTTCACAATG[-/TTC]TTCAATAGAACATGA | 55833 |
rs745541176 | in-del | -/T/TT/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993896 | TTCAGCTTTGCTTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55833 |
rs745552232 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949194 | ATAAATAAATAAAAA[-/T]TAAAATAAAATAATA | 55833 |
rs745552999 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986710 | GCAACGCAACTGCCT[A/G]CTTCTTCCCCCTAAT | 55833 |
rs745555770 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985235 | TATTTAAACAAATTT[A/C]TGGGGTACATGTGGT | 55833 |
rs745587416 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010937 | GGCTGAAATCTTTGT[A/G]GAAAAAGTATGAAAA | 55833 |
rs745607905 | in-del | -/AT | 0.00089923 | 0.021185 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922400 | AGGCATGGCTGACAC[-/AT]GTCGGGAATTCTAGG | 55833 |
rs745632916 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929189 | GCAGCTCTGACCAGT[A/G]CTCGCAAGTGTACTT | 55833 |
rs745643165 | snp | A/C | 5.00179e-05 | 0.00500065 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948627 | AATCCTCAACAATAC[A/C]GAATTTCTGCCCAAG | 55833 |
rs745645649 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019696 | ATTTTACTACACACA[C/T]ACACACACACACACA | 55833 |
rs745646874 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943162 | AGTGAAAGATCAGAC[A/C]TAAAAGGCCACATAT | 55833 |
rs745655190 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938798 | AAGACTCCATCTCAA[-/A]AAAAAAAAAAAAAAA | 55833 |
rs745664172 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985645 | GAGAGTGGAATGATA[C/G]TTACCAGAGGCAGAG | 55833 |
rs745697994 | in-del | -/T | 4.97022e-05 | 0.00498484 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933649 | CAGATGAAGTAGCTG[-/T]TAAGAAGCAGATCTG | 55833 |
rs745699196 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974847 | CGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 55833 |
rs745715586 | snp | G/T | 1.64811e-05 | 0.00287059 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923169 | GCCTTATCCTGGAAA[G/T]GAGAGGTAAACACTA | 55833 |
rs745729444 | snp | C/T | 3.29794e-05 | 0.00406061 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926568 | ATAAGAGGGGGGACA[C/T]GTAAAAGATTCTGAA | 55833 |
rs745736238 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048602 | GGGGAAAGTAGGAAG[A/C]AGCACAGGGCAACGT | 55833 |
rs745760902 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | UBAP2 | GRCh38.p7 | 9:33941758 | GCTACTGGACTAGCA[C/G]AATTCAGTGATGAGC | 55833 |
rs745797033 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959720 | TTTTTTTTAAAAAAA[-/G]GTTCTTCTAGTCAAA | 55833 |
rs745837123 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953417 | AGTTTCAAAGGAGTT[A/G]GCTTCTGAGGCTTGA | 55833 |
rs745862863 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031690 | GTATGTACCACCATG[C/G]CCGGCTAATTTTTGA | 55833 |
rs745871995 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950477 | TCAAAGACAAGGAAT[A/G]TCCCACTTGGATGGA | 55833 |
rs745886460 | in-del | -/AAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991307 | CTCTGTATCAAAAAT[-/AAT]AATAATAATAACGTA | 55833 |
rs745905304 | in-del | -/A | 1.69749e-05 | 0.00291327 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988956 | GAGAAAAAACTGAGG[-/A]GAAAGTCTGTACTTA | 55833 |
rs745920408 | snp | A/G | 3.30764e-05 | 0.00406659 | missense | UBAP2 | GRCh38.p7 | 9:33927844 | CTGCTGGATGCACTC[A/G]CGGGGGTCCCACCCA | 55833 |
rs745975219 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937746 | ACCCCGTCTCTATTT[-/A]AAAAAATACAAAAAA | 55833 |
rs745994336 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923897 | ATTCACGAAGGGCTG[C/T]TGGGCTGTGTGGTGG | 55833 |
rs746006235 | in-del | -/A | 3.303e-05 | 0.00406373 | intron-variant, splice-donor-variant | UBAP2 | GRCh38.p7 | 9:34017047 | GTTCCACAAAAACTT[-/A]ACCTGTACCACTTGT | 55833 |
rs746015152 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017434 | TACCACCAATTTTAA[C/T]CAGCAACCATTTTAT | 55833 |
rs746050644 | in-del | -/AAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040324 | ATGAGACTCTGTCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 55833 |
rs746060246 | snp | A/C/T | 9.88475e-05 | 0.00702958 | missense | UBAP2 | GRCh38.p7 | 9:33923979 | GATGCAGAGTCCCCA[A/C/T]GGCCAAACTTTGTGA | 55833 |
rs746078056 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014358 | AAAAAAGGTCAGGTG[C/T]GGTGGCTCACGCCTA | 55833 |
rs746083862 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006203 | CGCACCATTGCACTC[C/G]AGCCTGGGAGACAGG | 55833 |
rs746108091 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930512 | GGAAACATCAAGATA[-/C]ACTTGTGGGGATACA | 55833 |
rs746127501 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041915 | CTGTAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGA | 55833 |
rs746129014 | snp | G/T | 1.64838e-05 | 0.00287083 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971740 | GAATCTGAATAGTCT[G/T]CAGGATTAAATGTCC | 55833 |
rs746148242 | in-del | -/TAACTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024631 | AAACGGGTCAGAAAA[-/TAACTT]TAACTTTAACAGGAT | 55833 |
rs746158224 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952868 | AGATCTACTGTAGAA[-/T]TTTTTGATGTTTTGT | 55833 |
rs746160607 | in-del | -/GGAGGAAGAGGAGGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016239 | GGAGGAAGAGGAAGG[-/GGAGGAAGAGGAGGA]GGAGGAAGAGGAGGA | 55833 |
rs746194667 | snp | A/C/T | 3.29789e-05 | 0.00406061 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924042 | CTGCCCTTCCTCCAA[A/C/T]CAGAGAAAGGCCACA | 55833 |
rs746221826 | snp | A/C/G | 3.62517e-05 | 0.00425732 | missense | UBAP2 | GRCh38.p7 | 9:33922715 | GGAAGGTGGTGGTGC[A/C/G]GCAGCTGTGAGTGGG | 55833 |
rs746235158 | snp | A/T | 1.65168e-05 | 0.00287369 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935756 | CCATTGACCAACTGG[A/T]GTTTTCCACATCACG | 55833 |
rs746255245 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033046 | GTACAACTACTATGG[A/G]AAACAATTTGGAGGT | 55833 |
rs746272018 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958817 | ACAGGAGTTTGGGGC[C/T]GGAGTGAGCTGGCCA | 55833 |
rs746282565 | snp | A/G | 3.5937e-05 | 0.00423877 | missense | UBAP2 | GRCh38.p7 | 9:33922808 | GAGGCCAGGGGCCCA[A/G]TGGAGCCCAAGACCG | 55833 |
rs746333081 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925026 | GCCCAGGACTTGGGG[G/T]AAGTATGGCAGATAC | 55833 |
rs746344649 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938036 | AGTGTCTGGCTCTGT[C/T]ACCCAGGCAGGTGTG | 55833 |
rs746350615 | snp | A/T | 3.29516e-05 | 0.00405891 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935846 | ATACTTACTGTCTAG[A/T]GTCTGCTGACTTCGA | 55833 |
rs746406130 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970398 | GTACTCTCTTATTTT[G/T]TGGCTAGGGTTGATG | 55833 |
rs746406163 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942454 | ACAAAGTCAGCCAGG[-/C]CGGTGGCTCATGCCT | 55833 |
rs746418891 | snp | A/T | 3.29533e-05 | 0.00405901 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989022 | GTTGTTGTTTCCACG[A/T]CCACGACTCGATTCT | 55833 |
rs746428497 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956319 | TCAAGTGAATGCAAT[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs746444564 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014520 | TGTAATCCCAGCTAC[C/T]TGAGAGGCTGAGGCA | 55833 |
rs746453284 | in-del | -/AG | 1.74087e-05 | 0.00295026 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932643 | ACTAGAAGACAAAAC[-/AG]AGCGCCGTATGTCCA | 55833 |
rs746502470 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923387 | CCCTCACCTGTACTG[C/T]AGCCGTGCTGGCCAT | 55833 |
rs746511180 | snp | A/C | 1.6588e-05 | 0.00287988 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960789 | CCATTTCAAAAAAAA[A/C]AAAAAAGAAAGGTCT | 55833 |
rs746517093 | snp | A/G | 1.68284e-05 | 0.00290067 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989122 | CCTACAGTCTCCCAT[A/G]AAGTCTATCAGAGAG | 55833 |
rs746519718 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932958 | GAACGAGGGATCAAA[C/G]TTCCTATGCTCAACT | 55833 |
rs746540810 | snp | G/T | 1.64972e-05 | 0.00287199 | missense | UBAP2 | GRCh38.p7 | 9:33943547 | GCACATTTAATCCTG[G/T]GACATCTGCTGAACC | 55833 |
rs746568200 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966534 | TTGTGCTGAAGCTAT[C/T]GATCAATTTGGAGAG | 55833 |
rs746576917 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979012 | GAGGCCAAGGGAGGA[-/G]GGACTGCTTGGAGCC | 55833 |
rs746596776 | snp | A/G | 1.65743e-05 | 0.00287869 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922441 | TGGGCTCCCAAATAC[A/G]TGCTCGTGTGTTCTC | 55833 |
rs746601084 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988372 | TTCTTTCATAACTTA[G/T]CTACACTGACACACT | 55833 |
rs746621824 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960709 | TGCTTGAATCTGGGA[A/G]GCAGAGGTTGCAATG | 55833 |
rs746654300 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976715 | ATATTTTCTTTCTTA[A/G]GCTGGGAGCAGTGGC | 55833 |
rs746663503 | in-del | -/TAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010427 | AGAAACTCTGCCTCA[-/TAA]AAAAAAAAAAAAAAA | 55833 |
rs746684932 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021634 | AAGAATCCATTTGAT[-/TTT]TTTTTTTTTTTTTTT | 55833 |
rs746688756 | in-del | -/AC | 1.65141e-05 | 0.00287346 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923767 | ACCCAAGGCCAGGAG[-/AC]ACAGTCACACCCTCT | 55833 |
rs746695720 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945683 | AGACAGACATATATA[C/T]ACACACACTATATAC | 55833 |
rs746704437 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947982 | GGAAGACCCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs746713580 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973212 | TGAGAACCTTCCTGC[C/T]CCTCTCCCTCTGCCA | 55833 |
rs746731833 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926915 | CAACCTGGGCCCAAC[G/T]CCAGGTTCCTGCCAG | 55833 |
rs746773148 | snp | A/G | 1.69218e-05 | 0.00290871 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932623 | CTCTGGTGGCTGGAG[A/G]GCGAACTAGAAGACA | 55833 |
rs746836693 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972996 | TGCCAAGGCTAGAAA[C/G]CCTGCTCTAATGCCT | 55833 |
rs746840743 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984996 | ACAGGGAAAAGGGAA[C/T]TCTCATACACTATTG | 55833 |
rs746863125 | snp | A/G | 0.000124881 | 0.00790093 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933453 | CCAGGACTTGCCCCA[A/G]GGTACTTCTCACTTT | 55833 |
rs746874753 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013845 | ACGCGCCACTGCACT[A/C]CAGCCTGGGCGACAG | 55833 |
rs746879648 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | UBAP2 | GRCh38.p7 | 9:33924264 | CGCTGTGGGTGCAGC[A/C]AAGGGAATTCCATAG | 55833 |
rs746898456 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922953 | ATACACCCAACCCAC[C/T]TTTGTCCCTCACCTG | 55833 |
rs746944503 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923142 | GGATCAGGCAGGAGC[C/T]CACCACTCCAGGCCT | 55833 |
rs746956126 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949195 | TAAATAAATAAAAAT[-/A]AAAATAAAATAATAA | 55833 |
rs746960122 | in-del | -/A | 0.0918349 | 0.193607 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960781 | GTGAAATTCCATTTC[-/A]AAAAAAAAAAAAAAG | 55833 |
rs746961195 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950606 | CCAGATTCTTTTTTC[A/G]GGTTGCCCAATACAC | 55833 |
rs746973153 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981468 | TCAAGCCATCCTACC[A/G]CCTCAGCCTCCTGAG | 55833 |
rs747032698 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990825 | TAATTTTAGTAGAGA[A/C]GGGGTTTCACCATGT | 55833 |
rs747050127 | in-del | -/CAAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930895 | AGTGAGACTGCATCT[-/CAAAAAAAAAA]AAAAAAAAAAAAAGC | 55833 |
rs747073250 | snp | C/G | 2.04819e-05 | 0.00320009 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927099 | TATAGAGGGAAAAAT[C/G]AAATGGAGTGAAATG | 55833 |
rs747107128 | snp | C/G | 3.29489e-05 | 0.00405874 | missense | UBAP2 | GRCh38.p7 | 9:33941739 | GTCATAAGAGGAAGA[C/G]ATTGCTACTGGACTA | 55833 |
rs747118930 | snp | C/T | 1.64781e-05 | 0.00287033 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996312 | TGCATTCATCCTGAT[C/T]TTTCCCTGTCACTTC | 55833 |
rs747125190 | in-del | -/G | 1.64933e-05 | 0.00287165 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956152 | TTCAGAAAGCTGTAT[-/G]GGAAAGTTGAAAAAT | 55833 |
rs747151177 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039948 | CGATCACCTGAGGTC[A/G]GGAGTTCAAGACCAG | 55833 |
rs747192423 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017742 | CCATGCTGGCTAACA[A/C]AATGAAACCCCGTCT | 55833 |
rs747199580 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017789 | AAAGTTAGCCGGGCA[C/T]GGTGGCAGGCATCTG | 55833 |
rs747200147 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014090 | ACCTTGGGAGATCAA[-/G]GGGGGGGACAGATCA | 55833 |
rs747201609 | in-del | -/ATAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010426 | CAGAAACTCTGCCTC[-/ATAA]AAAAAAAAAAAAAAA | 55833 |
rs747218048 | snp | C/G | 1.66471e-05 | 0.00288501 | missense | UBAP2 | GRCh38.p7 | 9:33927829 | GCGGCCCTGCTACTG[C/G]TGCTGGATGCACTCG | 55833 |
rs747247398 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991322 | AATAATAATAATAAC[A/G]TAAGAATTGTTCAAA | 55833 |
rs747265457 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019386 | CCAGCCTGGGCGACA[C/G]AGCAAAACTCTCGGG | 55833 |
rs747301422 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003691 | GGATTACAGGCGTGA[A/G]CCACCACACACGGCC | 55833 |
rs747302155 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013487 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAATAAAA | 55833 |
rs747305920 | snp | A/C | 3.36581e-05 | 0.00410219 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963690 | GCAATTTATAAGATT[A/C]TTAATTTTAAAAATT | 55833 |
rs747354172 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923742 | GGTCCCAGGTTTCCA[C/G]CTGCCAGCAACCCAA | 55833 |
rs747372316 | snp | A/C | 3.30028e-05 | 0.00406205 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963820 | TAAAATTGAGGGTTT[A/C]AACATATGAAAAGAA | 55833 |
rs747377991 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970244 | CTTCCTGGAACCAAT[G/T]ATTCACGTTCTCACC | 55833 |
rs747385132 | snp | A/G/T | | | utr-variant-5-prime, intron-variant | UBAP2 | GRCh38.p7 | 9:34048841 | GCTGCTGCTCTCGGA[A/G/T]GACCCAAGACCCGCT | 55833 |
rs747393971 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969043 | TATTCCATTCTATGT[A/G]TATTCTATATTTTGC | 55833 |
rs747400367 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | UBAP2 | GRCh38.p7 | 9:33923959 | GTGTGGTAGCGGGTG[C/T]AGGGGATGCAGAGTC | 55833 |
rs747425376 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956379 | GAAGGAGTGCAGTGA[C/T]GTGATCTCGGCTCAC | 55833 |
rs747442478 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924925 | AAGCTCATCAGCTAT[A/C]TTTAATGTTAGTGTA | 55833 |
rs747452205 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025262 | CATAGGAATTCAGTG[C/T]ACACTTGTGTTCCAT | 55833 |
rs747453377 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041714 | CCGTCTTATAAAACA[A/C]AACAAAGAAAAAAGA | 55833 |
rs747465425 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933617 | CAGAGGGAGGGCCTG[C/T]TGTCTTTGGAGCTGG | 55833 |
rs747471455 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992183 | CACCTGAGGTTGGGA[A/G]TTCAAGACCAGCCTG | 55833 |
rs747498695 | in-del | -/CA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925227 | GCTGGGAATGGCACT[-/CA]CACCCTCCAGGAAAC | 55833 |
rs747502873 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953649 | CACAAAAGAACATAC[C/G]AAGCCACAGAGACTG | 55833 |
rs747515660 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950234 | CCACGCCCGGCTTTT[G/T]TGTTGTTGTTGTATT | 55833 |
rs747553647 | in-del | -/AGACCG | 1.7953e-05 | 0.00299603 | cds-indel | UBAP2 | GRCh38.p7 | 9:33922817 | GCCCAGTGGAGCCCA[-/AGACCG]AGACCGAGGGCAGGC | 55833 |
rs747627009 | snp | C/G | 1.64909e-05 | 0.00287144 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926610 | GACCAGTCCATACCC[C/G]ACTCACCACTGGCAG | 55833 |
rs747628457 | snp | C/T | 1.71965e-05 | 0.00293222 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988933 | GAGGGTCACTTGAGA[C/T]GAAAGAAGAGAAAAA | 55833 |
rs747635714 | snp | C/G | 1.6477e-05 | 0.00287024 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989017 | TTCCGGTTGTTGTTT[C/G]CACGTCCACGACTCG | 55833 |
rs747641480 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033933 | TAGAGACGGGGTTTC[C/G]TCATGTTGGCCAAGC | 55833 |
rs747663000 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944040 | TACTCTATTTTTGGG[-/G]ACTCACCAATGATGA | 55833 |
rs747665158 | snp | C/T | 1.65987e-05 | 0.00288082 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935742 | TTTTAACGAATAAGC[C/T]ATTGACCAACTGGTG | 55833 |
rs747683942 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005370 | AACCTGGGAGGCAGA[C/G]GGTGCAGTGAGCCTA | 55833 |
rs747712212 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000443 | CCAGTCTGGTTTCTT[-/A]AGTTTTAACGAAGGT | 55833 |
rs747721752 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021530 | TTTATTTTTAAAGCA[C/T]TCTCTCAGATATGAA | 55833 |
rs747735003 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951809 | CTCAAGTCCTTCTTA[C/T]CAATTCAGTGGACAC | 55833 |
rs747736444 | snp | A/G | 4.94246e-05 | 0.0049709 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923363 | CATGTGTCTCTGTCT[A/G]GGAAGTACCCCTCAC | 55833 |
rs747743371 | in-del | -/ATGTTGAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940440 | TGTTGAGCTGAAATC[-/ATGTTGAG]CTAAGCTATCATGTC | 55833 |
rs747750154 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050020 | TCGCCAGGGCTGATT[C/G]GGCTGATCTGGCTGT | 55833 |
rs747756271 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014414 | GGGGGCAGTCACTTG[C/G]GCTCAGGTGTTGGAG | 55833 |
rs747760727 | in-del | -/CC | 3.29554e-05 | 0.00405914 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923370 | TCTGTCTGGGAAGTA[-/CC]CCCCTCACCTGTACT | 55833 |
rs747779670 | in-del | -/AGAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953063 | TTGCTTTTTTCGTAG[-/AGAC]AGAGTTTTGCCCAGT | 55833 |
rs747791980 | snp | A/C | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049994 | TTCTGGCTATCTTGT[A/C]ACCCCATAGATCGCC | 55833 |
rs747822349 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | UBAP2 | GRCh38.p7 | 9:33923474 | TTGGCTGAGGCTGGA[A/G]GGACCTGGGGGGGCA | 55833 |
rs747832554 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958292 | AATATTCCCAGTGAA[-/G]TCCATTTTTGCCTGA | 55833 |
rs747839820 | in-del | -/GTAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999857 | GGGATTACTACGTAT[-/GTAT]GTATGTATGTATGTA | 55833 |
rs747841926 | snp | A/T | 1.64936e-05 | 0.00287168 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956057 | TTTGAATAACAAATA[A/T]AAGATGGCAAAAAGT | 55833 |
rs747851918 | snp | G/T | 1.69209e-05 | 0.00290864 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943382 | TTGATCTCTCTTAGG[G/T]TCTATTTTGCTTCAT | 55833 |
rs747859884 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923084 | TTCCCAGCTCCAGGC[C/T]CCCCACCTCCAGGAT | 55833 |
rs747881638 | snp | C/T | 1.66738e-05 | 0.00288732 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998913 | CACCAAAAGCATAAG[C/T]TAGATTCCAAAATCT | 55833 |
rs747909745 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966037 | CCTGACTGACGAAGC[A/G]AGACTCCATCTCAAA | 55833 |
rs747938452 | snp | A/G | | | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996257 | AGCAATATATTGATA[A/G]CTTTGTTCACATCTC | 55833 |
rs747942637 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046438 | CACGGGGTCAGGAGA[A/T]CAAGACCATCCCGGC | 55833 |
rs747942662 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | UBAP2 | GRCh38.p7 | 9:33943517 | GTTCTGACCCAAATT[C/T]CAGAGCCCCAAACTG | 55833 |
rs747947425 | in-del | -/A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007642 | TCCTTGTATGTTTTA[-/A/T]TTTTTATTTTTTTTG | 55833 |
rs747990149 | snp | C/G | 3.9604e-05 | 0.00444977 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928026 | GGACACATGGATCTG[C/G]AGGCAGAGGAGGAGG | 55833 |
rs747994305 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046100 | TAAGAATGAACGGGT[A/G]TTTGCTGACATACAG | 55833 |
rs747995510 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048231 | AAAAACCTACATTAA[A/G]TAATGAACTGTGATA | 55833 |
rs748018487 | snp | A/C | 1.66804e-05 | 0.00288789 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922434 | AGGGCACTGGGCTCC[A/C]AAATACGTGCTCGTG | 55833 |
rs748031090 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953231 | CATATTCTAGAATAC[A/G]TTTGCTAATGGGTAT | 55833 |
rs748037253 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969476 | ATGGCTTGAACCCAA[-/T]GGTTCAAGGCTACAG | 55833 |
rs748038628 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006800 | AACACAAGGAATATT[A/G]TTCTCATAATTCCTT | 55833 |
rs748075217 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016247 | AGGAAGGGGAGGAAG[-/A]GGAGGAGGAGGAAGA | 55833 |
rs748101199 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977461 | CATTGGTTTCTGTGT[A/G]TATACCATTTCCCTG | 55833 |
rs748107876 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968979 | ATACTATTTTCAAGG[C/T]TCATCCATGTTGTAG | 55833 |
rs748120336 | in-del | -/A | 1.72528e-05 | 0.00293703 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988924 | TGAGGCGGGAGGGTC[-/A]ACTTGAGATGAAAGA | 55833 |
rs748133720 | snp | C/T | 0.000247082 | 0.0111122 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973197 | CCCCATGCCTTGGGT[C/T]GAGAACCTTCCTGCC | 55833 |
rs748142548 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002330 | CACAATTTATTATGA[A/G]TATCTATATCACGTT | 55833 |
rs748156851 | snp | A/C | 4.94474e-05 | 0.00497205 | missense | UBAP2 | GRCh38.p7 | 9:33941669 | TGGTTCCTGGAGCTG[A/C]CTCTGATGAACTCAC | 55833 |
rs748175811 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973081 | GTATAGAAAACACTA[A/G]ATTCACCATGATGAC | 55833 |
rs748179322 | snp | A/C | 3.29603e-05 | 0.00405944 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935884 | CATGTCCATTCTATA[A/C]GGAAAAGAAGAGAAG | 55833 |
rs748209060 | snp | A/G | 1.78717e-05 | 0.00298923 | missense | UBAP2 | GRCh38.p7 | 9:33922839 | AGGGCAGGCTGAAAG[A/G]TGGAGGCGTCCCTGC | 55833 |
rs748271221 | in-del | -/AGCGGCGGTGGTGGTGGTGGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016365 | GGCAGCAGCGGCGGC[-/AGCGGCGGTGGTGGTGGTGGT]GGTGGTGGTGGTGGT | 55833 |
rs748274153 | snp | C/T | 8.24885e-05 | 0.00642164 | missense | UBAP2 | GRCh38.p7 | 9:33948581 | ATCCTGAGCCAAGGA[C/T]GGATGACTTTAAAAG | 55833 |
rs748297425 | snp | G/T | 3.29946e-05 | 0.00406155 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922939 | CCTCTCAAAAACCTA[G/T]ACACCCAACCCACCT | 55833 |
rs748308543 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928817 | GTCTCCAAACCAGGA[C/T]ATAGAAAGCAGCATA | 55833 |
rs748325139 | in-del | -/CTACTAAAAATA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014462 | GGTGAAACCCTGTCT[-/CTACTAAAAATA]CAAAAATTAACTGGA | 55833 |
rs748328493 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983735 | GTGCCAACACTCTTC[A/G]TTGCCATCTTTCTAT | 55833 |
rs748351319 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994768 | CTCAAACAGTGAAAT[A/C]TTTTCCACATTAGTT | 55833 |
rs748352109 | snp | A/C | 1.65241e-05 | 0.00287433 | missense | UBAP2 | GRCh38.p7 | 9:33941649 | TAAAATACCACTTAC[A/C]ATGATGGTTCCTGGA | 55833 |
rs748399667 | snp | G/T | 6.58989e-05 | 0.00573978 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996290 | TTACAATCATGTAGG[G/T]CCACTATGCATTCAT | 55833 |
rs748417402 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971580 | TTTAGACTTCATCTT[C/T]GTATGAGAACATACA | 55833 |
rs748426134 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029988 | CAAGACTCCATCTCG[A/G]AAAAAAAAAAAAGAA | 55833 |
rs748462010 | snp | C/T | 1.76256e-05 | 0.00296859 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989169 | TTATCATTCAAAGTG[C/T]GTACAATTATCAAAG | 55833 |
rs748467246 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBAP2, SNORD121B | GRCh38.p7 | 9:33934329 | AGTGCTGTCCACACA[C/T]ACAACTCAGATATGT | 55833 |
rs748482748 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33960837 | TTACATCTTCAGTCC[A/G]GTCTTCTGTTGTCCA | 55833 |
rs748483910 | snp | A/C | 1.64787e-05 | 0.00287038 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960901 | GAAACAACAGCAATC[A/C]AAGTTTATACCACAA | 55833 |
rs748492171 | snp | A/G | 5.69222e-05 | 0.00533459 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927085 | GGGTGCTTTGCCTGT[A/G]TAGAGGGAAAAATCA | 55833 |
rs748565824 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967952 | TGTTTTCACTACATA[G/T]TTCTTTACTGCTGCT | 55833 |
rs748566046 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979559 | CAGCCAGGGCAACAA[C/G]AGAGAAATTCCCGTC | 55833 |
rs748583824 | in-del | -/TG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931610 | TTGAAAGTGGCAGTT[-/TG]TGTGTTTTATGATAA | 55833 |
rs748594401 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988024 | CTCACCTCTTTCAGA[-/G]GGCTGACTCACATGA | 55833 |
rs748605126 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019004 | TGACATATATACACA[A/G]TGGAAAATTATTCAG | 55833 |
rs748658034 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036358 | CCGACCTCAGGTGAT[A/C]TGCCCGTCTCGGCCT | 55833 |
rs748695547 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947550 | GTCCAGGCCGGGCGT[A/G]GTGGCTCACACCTGT | 55833 |
rs748695775 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944476 | AAGCTGCAAAAGCTT[A/G]TTCACAGTGGAGGGA | 55833 |
rs748697412 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990515 | CTAAGCTTTAATAAT[A/G]AAGACTGAATATACT | 55833 |
rs748701438 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040545 | GAGCCCAGGAGTTCA[C/T]GACCAGCCCAGCCAA | 55833 |
rs748737944 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024087 | TACAAGGATGGGCGC[A/G]GTGGCACACGCCTGT | 55833 |
rs748761524 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981245 | ATATATATATTCTGG[-/AT]ATATATATATATATT | 55833 |
rs748764881 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956250 | TCTCTTACACTTCGC[A/G]TAACAGCTATTCTAA | 55833 |
rs748770599 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928818 | TCTCCAAACCAGGAC[A/G]TAGAAAGCAGCATAT | 55833 |
rs748771469 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999935 | GAGTCACACTCTGTC[A/G]CCCAGGCTGGAGTAT | 55833 |
rs748790054 | snp | A/G | 1.66139e-05 | 0.00288213 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933509 | TAAGCTGAGAGAGAG[A/G]GCTGCTAGTCAGGTC | 55833 |
rs748806758 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957215 | TTCATTTTTATTAAA[C/T]CATGAGTTTCTATTA | 55833 |
rs748833347 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012671 | TTAAGTGAAGAAGAA[A/C]CTTATTCACAACTAC | 55833 |
rs748841969 | snp | G/T | 1.64751e-05 | 0.00287007 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33986788 | TCGCTTGCCACGATC[G/T]GAAGGTTTGTCCACT | 55833 |
rs748844329 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924297 | GTCCTAGGAGAGACC[A/G]GGGAGGCTTGATCAG | 55833 |
rs748844619 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943405 | TGCTTCATAACAAAG[A/G]ACTAAATTCAGTACC | 55833 |
rs748921547 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005766 | AGCTATGGACAATAA[A/G]CCTCCAAAGAATAAA | 55833 |
rs748922852 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946088 | TTAATTGGTGGAAAA[C/T]GGTATTAAAAAATAC | 55833 |
rs748960251 | in-del | -/CAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008636 | AAAGCGTAAGATATA[-/CAC]TACTAACACTTTACA | 55833 |
rs748968871 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968807 | CATCACTCCAAAAAC[A/G]AACTCCATACTCATT | 55833 |
rs748985498 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017031 | GAAAAAAAAAAAAAG[-/G]AGTTCCACAAAAACT | 55833 |
rs749001491 | snp | C/G | 4.94972e-05 | 0.00497455 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953344 | TCCCTGGTGCCATCT[C/G]ATTGTTGTGTTGCGA | 55833 |
rs749008683 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998574 | AGTAACTCAGAAAGA[C/T]TATATTGTAAGGCAG | 55833 |
rs749032541 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013358 | AATTCAAGACCAGCC[C/T]GACCAACATGGTGAA | 55833 |
rs749052982 | in-del | -/A | 1.64732e-05 | 0.0028699 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33948480 | ACTTGGGGTGGTGGT[-/A]AACTGGCCCAAACTC | 55833 |
rs749061538 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931085 | ATATTATGAACAAAC[A/T]GTTGACCCCTGAACA | 55833 |
rs749094225 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953428 | AGTTGGCTTCTGAGG[C/T]TTGACTGTGAGGAAC | 55833 |
rs749103957 | in-del | -/A | 0.00011538 | 0.00759452 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973241 | ACGTCCAAATCCTTT[-/A]AAAAAAACACACAAT | 55833 |
rs749105679 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042332 | AAATACAAAAAATTA[C/G]CCAGGCGTGGTGGCG | 55833 |
rs749107285 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976391 | TCAGGGTAAAGGCGA[C/T]GGGGAACCCAAAACA | 55833 |
rs749110316 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032639 | AAGAATCTTTGTTTC[C/T]TAGGCTGGGTGTGGT | 55833 |
rs749111180 | snp | G/T | 1.69582e-05 | 0.00291184 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943377 | ACCAGTTGATCTCTC[G/T]TAGGGTCTATTTTGC | 55833 |
rs749137270 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037998 | AAACCCTGTCTCTAC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs749162885 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005038 | GAGGCTGAGGCAGGC[-/G]GATCACTTGAGGTCA | 55833 |
rs749176305 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923349 | AGCCTGTCTAACCCC[A/G]TGTGTCTCTGTCTGG | 55833 |
rs749187208 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985774 | TGCCTGTAATCCTAC[C/T]GCTTTGGGAGGATTA | 55833 |
rs749192852 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050250 | GCTAGTTACATACAA[C/G]GACTTTGCAGTCCCG | 55833 |
rs749196714 | snp | C/T | 1.65015e-05 | 0.00287237 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927920 | CTGAGGATGCGGAAC[C/T]TGAGACGGAGGTCGC | 55833 |
rs749200779 | in-del | -/TTG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002118 | CCATGCCTGGCTAAT[-/TTG]TTGTTGTTATTTTCA | 55833 |
rs749200931 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975015 | CAAATGACCAATAAA[C/T]ACATTAAAAGATACT | 55833 |
rs749206945 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048381 | AGAGAGCGCATAAGT[A/T]GGGGCTATAACAGGG | 55833 |
rs749262699 | snp | A/G/T | 4.94909e-05 | 0.00497428 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971744 | CTGAATAGTCTGCAG[A/G/T]ATTAAATGTCCTGGG | 55833 |
rs749283287 | snp | C/T | 1.66432e-05 | 0.00288467 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998907 | TTTGAACACCAAAAG[C/T]ATAAGTTAGATTCCA | 55833 |
rs749296035 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021318 | ACATTATAGTAACAA[C/T]CAATTATCTAGAATT | 55833 |
rs749297019 | snp | A/G | 1.86579e-05 | 0.00305428 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928011 | GCAAAAGAAAAGCCA[A/G]GACACATGGATCTGG | 55833 |
rs749297439 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014982 | AGCAGAATACTACAC[C/T]AACTTTATACTGAAA | 55833 |
rs749312680 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950703 | AGGTGATGACTCTCT[C/T]CATCCTGTTATCCTA | 55833 |
rs749319500 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982816 | GTAATAACAGTACCC[A/G]TCCTAACAGATACTC | 55833 |
rs749330150 | snp | C/T | 0.000131898 | 0.00811982 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926594 | CTGAACCCTCTGCTC[C/T]GACCAGTCCATACCC | 55833 |
rs749353605 | snp | C/T | 1.70775e-05 | 0.00292207 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948370 | ACAAACAATGTATAC[C/T]TACCAAGATGACTGA | 55833 |
rs749384501 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940551 | AAGAAGGCCAAGATA[A/G]GTGGATTGCGTGAAC | 55833 |
rs749399297 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028926 | TGAGCAAACCTGGGC[A/G]GCGTGGCAAGTCCTC | 55833 |
rs749412144 | snp | A/C | 1.64787e-05 | 0.00287038 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973177 | AATAGGATGGCTATC[A/C]CTTACCCCATGCCTT | 55833 |
rs749438152 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964888 | GGCATGTATATGAGT[-/A]CCTGTTATTCCACAA | 55833 |
rs749444181 | snp | A/G | 0.000161407 | 0.00898208 | missense | UBAP2 | GRCh38.p7 | 9:33922823 | GTGGAGCCCAAGACC[A/G]AGGGCAGGCTGAAAG | 55833 |
rs749448647 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044565 | AGACTGTCTCAAGAA[A/C]ATAAAAATAAAAGAA | 55833 |
rs749459651 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998934 | TCCAAAATCTGGGTC[A/C]AACAGATAAGGCTCT | 55833 |
rs749478197 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996117 | AAACAAATATGGAAT[G/T]GCACCATAATCCATT | 55833 |
rs749489607 | in-del | -/AAAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969562 | TCTTTAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 55833 |
rs749530624 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981934 | TCATAGTAATTTTCA[C/T]ATTATCTCTATGAAA | 55833 |
rs749554039 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951988 | ACTGACACCACCTCA[A/T]ATACCAATGATACTA | 55833 |
rs749567514 | snp | A/G/T | 3.29458e-05 | 0.00405857 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948471 | CTGCTGTGTACTTGG[A/G/T]GTGGTGGTAAACTGG | 55833 |
rs749597237 | in-del | -/TG | 1.64743e-05 | 0.00287 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923350 | GCCTGTCTAACCCCA[-/TG]TGTCTCTGTCTGGGA | 55833 |
rs749648373 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036098 | ATTTAATTGTAACTT[A/C]AGGAATTTGATACTT | 55833 |
rs749649081 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989422 | TAGCCATGATGGTCT[A/C]GATCTCCTGACCTCG | 55833 |
rs749658308 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945905 | TTTGTATGTAAGATA[C/T]TTTGTGCAAGTACAA | 55833 |
rs749663485 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935877 | CCACCACCATGTCCA[C/T]TCTATAAGGAAAAGA | 55833 |
rs749673351 | snp | C/T | 3.42812e-05 | 0.00413998 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989140 | GTCTATCAGAGAGAA[C/T]GGCTGTTAATCATTT | 55833 |
rs749682028 | snp | A/C | 1.67593e-05 | 0.00289471 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941633 | CTTCTGAGAAAAAAA[A/C]TAAAATACCACTTAC | 55833 |
rs749742790 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043748 | ATCCTTCCACCTCAG[C/G]CTCCCAAAGCGTTGG | 55833 |
rs749812506 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021881 | TCGGGTGATCCAACC[A/G]CCTCAACCTCCCAAA | 55833 |
rs749817554 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972554 | CTTGGAGCCAATTCC[C/T]TTCCTTGACTGCATC | 55833 |
rs749817638 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959315 | ATTAAACAAGTCAAG[C/T]AGAAATCATGTTTCT | 55833 |
rs749831661 | snp | C/T | 1.6519e-05 | 0.00287388 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960803 | AAAAAAAAGAAAGGT[C/T]TCATCTGACAGCAAA | 55833 |
rs749860124 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034181 | TAAAAGTTCAACATA[C/T]CTATTAAGTCATTTT | 55833 |
rs749866860 | in-del | -/AAAAATTA | 5.85069e-05 | 0.00540833 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963699 | AAGATTCTTAATTTT[-/AAAAATTA]AAAAATTAAGTATTC | 55833 |
rs749876133 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002086 | CTCAGCCTCCTGAGT[A/T]GCAACCATGGCAGCC | 55833 |
rs749890920 | in-del | -/CGGGGAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960963 | TTTTTGTGTACTATG[-/CGGGGAAAAAA]GATACATACGCCTCA | 55833 |
rs749898112 | snp | A/C | 1.66427e-05 | 0.00288462 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998750 | GCACAATCAAAATAG[A/C]TTATAAAAATGATGA | 55833 |
rs749931187 | snp | A/T | 1.64746e-05 | 0.00287002 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941826 | TGTGGAGTTCTGTAC[A/T]GCACTGGTCATTGAT | 55833 |
rs749948639 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941639 | AGAAAAAAACTAAAA[C/T]ACCACTTACCATGAT | 55833 |
rs749951342 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968678 | AATACTAATTTCTAT[A/G]TTTTTATATACAATA | 55833 |
rs749952991 | snp | A/G | 1.64904e-05 | 0.00287139 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33963789 | GAGTATTTGATGCCA[A/G]TTCTGTGGACCAATG | 55833 |
rs749965526 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | UBAP2 | GRCh38.p7 | 9:33923853 | TAGTAGGGAAGACCA[C/G]TGTAGCTATAGCCAG | 55833 |
rs749969829 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935000 | TCCGCACTCCCAGGA[A/T]ATCCTATTTAAAGAG | 55833 |
rs750005017 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980122 | TCTTCAAGCAAAGCT[G/T]GCAAACACATACTTA | 55833 |
rs750019244 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | UBAP2 | GRCh38.p7 | 9:33927875 | GACAGAGGCTGTTCG[C/T]GGTGTTCATGCTACT | 55833 |
rs750032148 | snp | A/T | 3.29478e-05 | 0.00405867 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923933 | TGATTGGCTCTGCTG[A/T]GGCTGAGCTGGTGTG | 55833 |
rs750038677 | snp | A/T | 1.64751e-05 | 0.00287007 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33971679 | TGCACCATTCTGAGC[A/T]GCTTCCCAAACTACT | 55833 |
rs750040777 | snp | A/C | 3.29641e-05 | 0.00405968 | missense | UBAP2 | GRCh38.p7 | 9:33944523 | ATTCTCGAAGTTTTG[A/C]CTGGGAAGGAAAGGA | 55833 |
rs750092722 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968278 | TTCCATAATATACTG[-/T]CCATTTACTCTGTAC | 55833 |
rs750097747 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041056 | TCCACATGAGGACAA[A/G]TAAAATTGGTAATCT | 55833 |
rs750117262 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991557 | TTAGTTCAAATAGGA[G/T]CCTATGTACTTACTG | 55833 |
rs750143355 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950812 | GACTACTGCCATGTC[C/T]TAGGTAATACACAGC | 55833 |
rs750179078 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974988 | AATATGGATTTCTCC[A/G]AAGAAGATATACAAA | 55833 |
rs750197796 | snp | A/G | 3.29723e-05 | 0.00406018 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933595 | AGGGAGCTCACAGAC[A/G]GGAGGGCAGAGGGAG | 55833 |
rs750204572 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000513 | ACAGGAACAATCTGT[A/G]TCATCTCTGTACAAC | 55833 |
rs750210337 | snp | A/C | 3.30153e-05 | 0.00406283 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986865 | GAGCAGAAAAATCAA[A/C]TTTCCATTTCCAAAC | 55833 |
rs750215274 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032485 | AAGGAGGAAAACCAC[C/T]TTCCCCCTTTGGCCA | 55833 |
rs750222996 | snp | A/T | | | missense | UBAP2 | GRCh38.p7 | 9:33944382 | TAGAAGCTGGGGGTA[A/T]CCGCCGCTTAGCAAG | 55833 |
rs750238859 | snp | A/G | 7.21826e-05 | 0.00600717 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922774 | GAATGGTGGGGGTGC[A/G]TAGCCAGGGGCCGCT | 55833 |
rs750241206 | snp | A/C | 2.88305e-05 | 0.00379663 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935711 | GGTCCAAAAACAAAA[A/C]AGCAAAAGGGCTGCT | 55833 |
rs750307339 | in-del | -/TAAG | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050423 | CGGGCCCAAAAGGTC[-/TAAG]TAAGGTAGAAAGGGG | 55833 |
rs750309191 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013241 | GGACAAAAATCCTGG[C/T]TTATACGGATTCAAA | 55833 |
rs750323827 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983766 | CTTTGACAATAGTAA[A/G]TTTGAAACTTACTTT | 55833 |
rs750331847 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924368 | CATGGAAGTGGTGAC[A/G]CCACACTCCTGAAAC | 55833 |
rs750364208 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014077 | CCTGTAATCCCAACA[C/T]CTTGGGAGATCAAGG | 55833 |
rs750395787 | snp | A/G | 1.69786e-05 | 0.0029136 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926953 | CCCCCGAGGCCAGGG[A/G]AGCTGGGCAGGCCAG | 55833 |
rs750403723 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923338 | TGAGCCAGGCAAGCC[C/T]GTCTAACCCCATGTG | 55833 |
rs750446632 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049656 | CGGTTTTACTTTTGC[C/G]CTCCCAAGCCCCTTC | 55833 |
rs750464960 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964220 | TTCTGAGCCTATAAG[A/G]CTGAGTCCTGGACTC | 55833 |
rs750474628 | in-del | -/AGGCCAGGGGAGCTGGGC | 1.70583e-05 | 0.00292042 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926944 | AGGTGCCAGCCCCCG[-/AGGCCAGGGGAGCTGGGC]AGGCCAGGAGTTCCG | 55833 |
rs750521740 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002380 | ACTGCATAGGTGCTT[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs750547801 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978017 | GAGACTCTGTCTTTT[-/A]AAAAAAAAAAAAAAA | 55833 |
rs750563543 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021299 | TATTATTGTACTGCC[G/T]TTTACATTATAGTAA | 55833 |
rs750569058 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923435 | AAGGGAGGTGTGGGA[A/G]TGCTGAGGTTCACCC | 55833 |
rs750579800 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986396 | GACTACAACTCACTG[-/A]AAGCTCAAATGATCA | 55833 |
rs750586076 | in-del | -/GGGTC | 1.6473e-05 | 0.00286988 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33923276 | CTGCTGCTGTCCCCT[-/GGGTC]AGGTCGTCATAACCT | 55833 |
rs750589488 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965396 | TTTCTCCAAGACTAC[A/G]TCTCATTCTATCATT | 55833 |
rs750595938 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013152 | GTGAGACTCTAGCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs750600548 | snp | C/T | 1.74467e-05 | 0.00295348 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927986 | AGGCGCTCTCCACAC[C/T]GGCATGCTGGCAAAA | 55833 |
rs750612104 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033308 | AGATCCTGTCATTTG[A/C]AACAACGTGGATAGA | 55833 |
rs750619330 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004732 | GAGCTTGCAGTGAGC[C/T]GAGATAGCGCCACTG | 55833 |
rs750650127 | snp | C/G | 1.64811e-05 | 0.00287059 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017070 | CCACTTGTTTCTGTG[C/G]TTGCGTTGATTGTGC | 55833 |
rs750675071 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985313 | GGATATCCGTTACCA[C/T]GAGCATTTATCATTT | 55833 |
rs750676532 | in-del | -/CAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992003 | TCACACCTGTAATCC[-/CAG]CACTTTGGGAGCCCA | 55833 |
rs750761581 | snp | G/T | 4.97426e-05 | 0.00498686 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932562 | CGCGCAGACACTTAC[G/T]GTGTGTGACGTGCTC | 55833 |
rs750767612 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954016 | GGCTTAAGCGATTCT[C/T]GTGCCTCAGCCTCCC | 55833 |
rs750780610 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029754 | CAGCACTTTGGGAGG[C/G]CAAGGCAGGTGGATC | 55833 |
rs750796235 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015579 | TGATCTGTCCACCTC[A/G]GCCTCCCAAAGTGCT | 55833 |
rs750797076 | snp | A/T | 1.66638e-05 | 0.00288645 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017162 | ATATACAGTATATAC[A/T]AAATAATGTATGTAC | 55833 |
rs750802070 | snp | A/C | 1.64863e-05 | 0.00287104 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973160 | AAGTAAATAATTATA[A/C]AAATAGGATGGCTAT | 55833 |
rs750818508 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948462 | TGTACTATTCTGCTG[C/T]GTACTTGGGGTGGTG | 55833 |
rs750819782 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027488 | CTGGGAGGCCAAGAG[C/G]GGGAGGATCGCCTGA | 55833 |
rs750824789 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945265 | ACACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 55833 |
rs750832932 | snp | A/C | 4.94727e-05 | 0.00497332 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973253 | CTTTAAAAAAACACA[A/C]AATTATAGTATAAAA | 55833 |
rs750852300 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972435 | ATCCCTCCTTTTCCT[C/G]AAAGGAGCTTAGGCA | 55833 |
rs750864713 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941284 | TAACACAAAAATACC[C/T]AACAGTGATGAAGAA | 55833 |
rs750880901 | snp | A/G | 5.04248e-05 | 0.00502094 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922907 | AAGACAATGGTGAAG[A/G]TCAGGTTGGGCTGTA | 55833 |
rs750890364 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995259 | CTACTTGGGAGGCTG[A/C]GGCAAAAGAATCACT | 55833 |
rs750920324 | snp | A/C | 1.64781e-05 | 0.00287033 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923008 | CATATCAGGTAGACC[A/C]GTGGTGCTTGAAGAC | 55833 |
rs750924538 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | UBAP2 | GRCh38.p7 | 9:33948542 | TGGTGATGTTTGCCA[C/T]TTTTGGTGGTGCAAG | 55833 |
rs750930066 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989435 | CTCGATCTCCTGACC[C/T]CGTGATCTGCCCGCC | 55833 |
rs750930814 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952955 | GCTCACTGCAACCTC[A/C]AACTCCTGGGCACAA | 55833 |
rs750943644 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982674 | ACCATACCCCCTGCA[C/G]AATTTATCTAGCATA | 55833 |
rs750977433 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961058 | AAAATCAGTAATATT[C/T]CTTTTCTCCCCTTCT | 55833 |
rs750999640 | snp | A/G | 1.74534e-05 | 0.00295405 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941607 | CATTAATTTCCAAAT[A/G]AGACGGACATCTTCT | 55833 |
rs751027397 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989873 | CCATTATTCAAACTA[A/T]TTATCTAAAACAATT | 55833 |
rs751042084 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037390 | TCCACTTGCCTTGGT[C/G]TCCCAAAGAGCTGGG | 55833 |
rs751098903 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947252 | GAACAGAGGAATATG[C/T]TTCCCTGTCTCTCTA | 55833 |
rs751100840 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003963 | GACCTCAGGTGATCC[A/G]CCCACCTCGGCCTCC | 55833 |
rs751134964 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941700 | AGGGCTTTGGTATGG[A/G]ATCCTGTTATGCACA | 55833 |
rs751153073 | snp | A/G | 1.7719e-05 | 0.00297644 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927788 | AGGAAAGGCCTCTGG[A/G]GCAAATACCTGAGGT | 55833 |
rs751171092 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996375 | GAGGCAAACAAAAAA[C/T]TGGCACTTGATATTA | 55833 |
rs751181773 | snp | A/G | 3.29571e-05 | 0.00405924 | missense | UBAP2 | GRCh38.p7 | 9:33960875 | ACAGAATTCTTCCAA[A/G]CCCCTGTTGGGAAAC | 55833 |
rs751191735 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016540 | ATTCTTCATTACCTA[C/G]TTTTTATTTTTTATT | 55833 |
rs751217807 | snp | C/T | 8.41616e-05 | 0.00648643 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017182 | AATGTATGTACAAAA[C/T]AGAAAATCTGCAAGA | 55833 |
rs751224735 | in-del | -/TTACAGAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009371 | CCCAAAGTGCTGGGA[-/TTACAGAC]GCAAGCCACCACACC | 55833 |
rs751244440 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042478 | GCAAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs751246610 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018286 | GATAAAGACCAGAAA[A/T]CCTGCTAGACAAATT | 55833 |
rs751271286 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035768 | CTCCTCAATAAAATG[C/T]AAACTGTTTATTCCT | 55833 |
rs751275215 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037751 | ATCATTCAGTAGTGT[A/G]CTTCAGTCACAATAT | 55833 |
rs751320666 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951611 | CTCGGCCTCCCAAAG[C/T]GCTGGAATAACAGGT | 55833 |
rs751334870 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923093 | CCAGGCTCCCCACCT[C/G]CAGGATCACTCAGGG | 55833 |
rs751351900 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999183 | GAGAAAGCAGAAGAA[C/G]AAAAAATAATAAAAT | 55833 |
rs751362950 | snp | A/G | | | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948438 | AGAAGTAGTAGTTGT[A/G]GGGTGACTTGTACTA | 55833 |
rs751366766 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934864 | CTCAGAACGACCAAC[A/G]AATCTCCAAACAGCC | 55833 |
rs751374209 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | UBAP2 | GRCh38.p7 | 9:33944513 | CCAGGTGTTGATTCT[C/T]GAAGTTTTGCCTGGG | 55833 |
rs751412240 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036318 | GATGGGGTTTCTCCA[C/T]GTTGGTCAGGATGGT | 55833 |
rs751453381 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040822 | TAGAATGAAATTCAT[C/T]ATGTACCATCCTTGA | 55833 |
rs751481975 | snp | A/G | 1.80748e-05 | 0.00300618 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922664 | GCCCAGAGTAGGGTG[A/G]CTGCCTCCATCACTG | 55833 |
rs751491007 | snp | C/T | 3.29495e-05 | 0.00405877 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986777 | CTACCCCGGGCTCGC[C/T]TGCCACGATCTGAAG | 55833 |
rs751493322 | snp | A/G | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934018 | TCAAAGGGCACAGCA[A/G]GGGGGAGTAAGAAGC | 55833 |
rs751502034 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033685 | TGCGCTCAAGAGATT[C/T]TCCCACCTCAACCTC | 55833 |
rs751530362 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975187 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCCGAGGC | 55833 |
rs751539482 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979175 | CGTAAGAGTTGGAGG[C/T]TGCAGTGAGCTATGA | 55833 |
rs751590605 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959580 | TTGGGTTATTTATCC[A/C]TTTTTTCTCTTTATT | 55833 |
rs751605574 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933026 | AGCTAAAGAGTGATG[C/G]AGAACACTCCTCAGA | 55833 |
rs751620810 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974601 | TATATCTGATCACAG[A/G]GTAACATCTGGAACA | 55833 |
rs751639876 | snp | C/G/T | 3.29708e-05 | 0.00406011 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953415 | GAAGTTTCAAAGGAG[C/G/T]TGGCTTCTGAGGCTT | 55833 |
rs751640312 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020969 | TCTGTTTTCTAGAAC[A/G]GTCAGTTTTAGACAC | 55833 |
rs751663636 | snp | A/G/T | 7.06221e-05 | 0.00594197 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935697 | CACAGCCAACACCTG[A/G/T]TCCAAAAACAAAAAA | 55833 |
rs751673230 | snp | A/C | 0.000199197 | 0.00997791 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923332 | CAAGTGTGAGCCAGG[A/C]AAGCCTGTCTAACCC | 55833 |
rs751677030 | in-del | -/A | 1.64958e-05 | 0.00287187 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923137 | GAGGGGATCAGGCAG[-/A]GAGCCCACCACTCCA | 55833 |
rs751686185 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987237 | CTAACACACGGAAAC[C/G]CTGTCTCTACCAAAA | 55833 |
rs751689668 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943055 | TGTCCACCAACTAAT[C/G]AATGAATAAAATGTG | 55833 |
rs751724055 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930772 | ATGGTGGTATGCGCC[A/T]GTAACCCCAGCTACT | 55833 |
rs751726196 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | UBAP2 | GRCh38.p7 | 9:33923239 | TGCGATGATCCAGCA[C/T]AGCCACCTTTGGAGT | 55833 |
rs751727567 | snp | A/G | 1.67716e-05 | 0.00289578 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953489 | GCTAAGCAGACAAAA[A/G]GCAATGAGGAACCAG | 55833 |
rs751743832 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941850 | CATTGATAAAGATGT[A/G]TTCAAAGGCTCACTG | 55833 |
rs751753468 | snp | C/T | 3.30055e-05 | 0.00406222 | missense | UBAP2 | GRCh38.p7 | 9:33926649 | GCAGCATCTGGAGCT[C/T]GTCATAGCCATAGAT | 55833 |
rs751755874 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020856 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 55833 |
rs751775996 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049227 | AGGTTACTCCCCTGT[A/G]GCCGCCCTGTGCTCA | 55833 |
rs751804394 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007799 | ACCCGCCACCACTCC[C/T]GGCTAATTTTTTTTT | 55833 |
rs751816570 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951444 | CTCCACCTCCCGGGT[A/T]CAAGTGATTCTCTTG | 55833 |
rs751820108 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000377 | TTTACCAACAAAAAA[A/T]CAGAAAAGTTCTAAA | 55833 |
rs751853002 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927902 | TACTGGACAGGCTGG[C/T]GCCTGAGGATGCGGA | 55833 |
rs751875436 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032296 | AAGAACAAATTAACT[C/T]ATAGATTTAATACCA | 55833 |
rs751897905 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964983 | CTCAATGTGGCTTTA[C/T]TTTGTATTTCTCCAA | 55833 |
rs751903264 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | UBAP2 | GRCh38.p7 | 9:33943462 | GGAATCTGATTACTA[C/T]TTTCACTGCTTGGAG | 55833 |
rs751915594 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994934 | ATTAAATCTGAACAC[C/T]GACACGGTCAGTTTG | 55833 |
rs751924134 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045024 | AATTAGTTATCAAAA[A/C]ATGGAAACTTATCAA | 55833 |
rs751982106 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:34017056 | AAAACTTACCTGTAC[C/T]ACTTGTTTCTGTGGT | 55833 |
rs751985895 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923317 | GCAGGGTACAAGAGG[C/G]AAGTGTGAGCCAGGC | 55833 |
rs751986041 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33971724 | CACATCTGTAGATGT[A/T]GAATCTGAATAGTCT | 55833 |
rs752031907 | snp | C/G | 1.70828e-05 | 0.00292252 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927978 | GTGGGAAGAGGCGCT[C/G]TCCACACTGGCATGC | 55833 |
rs752031935 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952874 | ACTGTAGAATTTTTT[A/G]ATGTTTTGTTTTAGA | 55833 |
rs752034807 | in-del | -/G | 8.39384e-05 | 0.00647782 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960796 | AAAAAAAAAAAAAAA[-/G]AAAGGTCTCATCTGA | 55833 |
rs752039987 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964080 | AATCTGTTCAACAGG[C/T]ACCAGTTTTTAGAAA | 55833 |
rs752048553 | snp | C/T | 1.64875e-05 | 0.00287115 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924039 | CCACTGCCCTTCCTC[C/T]AACCAGAGAAAGGCC | 55833 |
rs752069688 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973143 | CAGAATAAAAACTAG[C/G]GAAGTAAATAATTAT | 55833 |
rs752075669 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007557 | GTTGTTGATAATCTT[C/T]ACCACAAAGGGATGT | 55833 |
rs752088713 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972215 | TTTTGTTCAGCACCT[C/G]TATTTCTTTTCAATA | 55833 |
rs752089016 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945779 | CATACTCATTTTGGT[A/G]ACTACACAGAAATCT | 55833 |
rs752123544 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | UBAP2 | GRCh38.p7 | 9:33948440 | AAGTAGTAGTTGTAG[C/G]GTGACTTGTACTATT | 55833 |
rs752137837 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001616 | TGGTCCACTGACTCT[A/C]AATTTAGTTGGGTAT | 55833 |
rs752143649 | snp | C/T | 3.60198e-05 | 0.00424366 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922792 | GCCAGGGGCCGCTCC[C/T]GAGGCCAGGGGCCCA | 55833 |
rs752147743 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988845 | AGAATGTATGGAAAC[G/T]AAGAAAAAATTTGAG | 55833 |
rs752162070 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945394 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGCC | 55833 |
rs752167690 | snp | A/G | 0.000200622 | 0.0100135 | missense | UBAP2 | GRCh38.p7 | 9:33927036 | CGAGGTACTGGTTGT[A/G]CAGCAGGGGAGGCAC | 55833 |
rs752187231 | in-del | -/GAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928394 | CAAAGCAAACAGTCT[-/GAG]AAGAGGCGAGCACAG | 55833 |
rs752283903 | snp | A/C/T | 0.000117227 | 0.00765514 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926982 | AGGAGTTCCGCCATA[A/C/T]ACTCACCGGGTAGGC | 55833 |
rs752294480 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940018 | GGGAAAGAGGAGGGG[A/G]AGGGAGAGGAGGGAG | 55833 |
rs752294529 | snp | G/T | 3.45447e-05 | 0.00415586 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922886 | TCAAAAGTCTACAGG[G/T]CAAAGAAGACAATGG | 55833 |
rs752316208 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33948507 | ACTCGGAGCTTTCAA[A/C]TGGTCCAAAATCTGG | 55833 |
rs752319148 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959777 | GAGCAAACTTATTCA[A/G]GTTAATTTCAACTGT | 55833 |
rs752322638 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993533 | AATGATTAGCCAAGC[A/G]TAGTGGCATGCGCCT | 55833 |
rs752325134 | in-del | -/ACAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007584 | ATGTTGAATTTTTTC[-/ACAT]ACATTTTTCAGCGTT | 55833 |
rs752330529 | snp | C/T | 0.000281611 | 0.0118628 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938879 | CCATCTGTCAGGATA[C/T]AGACTCTAACTTATT | 55833 |
rs752378282 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011631 | AGGGAAGTTACCAGG[-/C]TGAGCTCTAGGAAGT | 55833 |
rs752415848 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024511 | TAATTCCCTATTCAT[A/G]AAAAGTCTTAATATT | 55833 |
rs752417841 | snp | C/T | 1.65304e-05 | 0.00287488 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996213 | ATGCAAATCAATTAA[C/T]AATACTTACTGTGTC | 55833 |
rs752422471 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971186 | TTACCCCAAGAATTT[C/T]AGAAAATAAATAATC | 55833 |
rs752432480 | snp | C/T | 1.66974e-05 | 0.00288936 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989108 | TCTTTTTCTTACACC[C/T]TACAGTCTCCCATGA | 55833 |
rs752438398 | snp | A/C | 1.64787e-05 | 0.00287038 | missense, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33960862 | TGTCCACTCTTCCAC[A/C]GAATTCTTCCAAGCC | 55833 |
rs752453704 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959551 | ACAGAAAAGAGGTAT[A/G]AAATTTTATGGTATT | 55833 |
rs752493193 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931337 | GTCACAGTTCTGTCA[C/T]GCTGACAAAGTATGG | 55833 |
rs752512307 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932796 | CCCAGTGATGGGGTC[C/T]TGGTGGACGGGAATG | 55833 |
rs752521686 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010757 | TAAACAGGAGCTACA[A/G]CAAACATTTTTTTTT | 55833 |
rs752522445 | snp | C/T | 1.67295e-05 | 0.00289214 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956195 | TACATACTACTAAAC[C/T]CAAAACACTGACTTC | 55833 |
rs752529541 | snp | C/G | 0.000595464 | 0.0172446 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923749 | GGTTTCCACCTGCCA[C/G]CAACCCAAGGCCAGG | 55833 |
rs752541757 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966992 | ACTAAATGTCACAAC[A/G]GTGGGACTAAAATAT | 55833 |
rs752544170 | snp | A/C | 3.3232e-05 | 0.00407614 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944338 | AATTCCAGCTTTAGG[A/C]CGGTGACTTCATGAT | 55833 |
rs752545511 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979057 | AGCCTGGGCAACACA[C/T]AGAGACCTGCCTACA | 55833 |
rs752564823 | snp | C/T | 2.10312e-05 | 0.00324271 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922496 | CAGCCCACCCCTCTC[C/T]TCTGGGTTTAGTTTG | 55833 |
rs752564909 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955450 | TTGAACTCAGGACGG[-/C]CGGGGGTTGCAGTGA | 55833 |
rs752599980 | in-del | -/A | 5.11261e-05 | 0.00505573 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922896 | CAGGGCAAAGAAGAC[-/A]AATGGTGAAGGTCAG | 55833 |
rs752602407 | snp | C/T | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922116 | TTCATTGGTACCTGA[C/T]CCCTATACCCAAACA | 55833 |
rs752624640 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035427 | GAACAGCTTGAACCT[A/G]GGAGGTGGAGGTTGC | 55833 |
rs752631866 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944440 | GACAGACACAGAGAT[A/G]TTTTCAATGGTCGTG | 55833 |
rs752638114 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946998 | CTAACCTATTAAGAG[C/T]GGCTCACTGTGCTAA | 55833 |
rs752688342 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038434 | ATTGCAGGCGCGCGC[C/T]GCCACACCTGACTGG | 55833 |
rs752700678 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989746 | CCAAGCTCCTATTCT[A/C]CACCACCTCACTTAC | 55833 |
rs752702721 | in-del | -/CT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982174 | AGCAGCCAGCAGCCC[-/CT]CTTTCACCCAAGCTG | 55833 |
rs752707015 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030005 | AAAAAAAAAAAGAAA[G/T]AAATACATACATAGG | 55833 |
rs752710693 | snp | A/C | 0.000270414 | 0.0116247 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922588 | GGGCTGGCTGCGCTG[A/C]CCCGAGCCACTCTGA | 55833 |
rs752721700 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955224 | AGTGAAAATAGCAAC[C/T]ATTAAAAAAGTTTAG | 55833 |
rs752749476 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023688 | AAGTTTTTCTCTTAA[G/T]TAAGGTTTACTGCTC | 55833 |
rs752768859 | in-del | -/AGAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945656 | TATCACAATATATAT[-/AGAC]AGACAGACAGACAGA | 55833 |
rs752793892 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047298 | CAGTTTGGGAAACTA[A/G]TCACTTCTGCCTAAT | 55833 |
rs752803834 | snp | G/T | 1.79264e-05 | 0.00299381 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932663 | GCCGTATGTCCACCT[G/T]AACAAGTGACTCCAG | 55833 |
rs752808230 | snp | C/T | 1.65261e-05 | 0.0028745 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924320 | TTGATCAGCGACTGG[C/T]CCTGCTTGACTCCCA | 55833 |
rs752813088 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984806 | CAATGAGATATCATC[C/T]TACCCCAGTTAGAAC | 55833 |
rs752822424 | snp | A/G | 3.45817e-05 | 0.00415809 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953273 | TCCCACACTGAAATA[A/G]AAGTGAGTTACCAGG | 55833 |
rs752828613 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954506 | ATGCACCGTATTACC[C/T]AACCTTGTAATGAAT | 55833 |
rs752859398 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959920 | AAAAAAAAATCAATC[C/G]TACTTAACACCTGGT | 55833 |
rs752870159 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973465 | ATCCTTGTATTATAT[C/T]TGTGGTATTTGACAG | 55833 |
rs752874917 | snp | C/G | 4.94768e-05 | 0.00497352 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986841 | CTTCACCTCTAACTA[C/G]GGGGAAAAGAGCAGA | 55833 |
rs752888638 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33924256 | CTGGCAAGCGCTGTG[A/G]GTGCAGCAAAGGGAA | 55833 |
rs752892544 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942917 | GAATGGTTAAGTTAC[C/T]ATATGACTCAGCAAC | 55833 |
rs752895496 | snp | A/G | 1.65151e-05 | 0.00287355 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933541 | CCAGTGTGCTGGGAT[A/G]TGGACGGCAGAAGTG | 55833 |
rs752910803 | snp | A/T | 1.64961e-05 | 0.00287189 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923061 | GCAGTTGTTCCCCAC[A/T]GCAGTTGTTCCCAGC | 55833 |
rs752932371 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012148 | TTCATAATTGTGGAA[C/T]GTTCACATAATTTTG | 55833 |
rs752939412 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045226 | CGGCAGGCGCCAGTA[G/T]TCCCAGGTACTCGGG | 55833 |
rs752947862 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986212 | TGCGTGCCACCACAC[G/T]TAGCTATTTTTTATA | 55833 |
rs752956560 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936130 | TGGGACTACAGGTGC[A/T]TCCTACCATGCCTAG | 55833 |
rs753002757 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961932 | ATGTACCTGATTTCA[C/G]ATTGGGGTGGCTCTC | 55833 |
rs753021166 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048093 | AACTCAGGGGAAAAT[A/G]TGGAAAAGCCGAGTG | 55833 |
rs753036146 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953374 | AATTTGTGAAGACAA[A/G]GGCTTGGCCAAAGCC | 55833 |
rs753070163 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020864 | GACGGGGTTTCACCG[-/T]TGTTAGCCAGGATGG | 55833 |
rs753092526 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944077 | CACCTGGTCAAGGAA[A/C]CATGCATCCTCCAAC | 55833 |
rs753095226 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005937 | TATTCTTTAGTTTAA[A/G]AACTGGACTCTGGCC | 55833 |
rs753123275 | in-del | -/C | 1.65526e-05 | 0.00287681 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33927842 | GCTGCTGGATGCACT[-/C]CGCGGGGGTCCCACC | 55833 |
rs753130093 | in-del | -/AATATATAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035514 | TAAAAAAAAAAAAAA[-/AATATATAT]ATATATATATATAAA | 55833 |
rs753154847 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032236 | CTCGCCAACCATGTT[C/T]AGCTGCAGGAATCCC | 55833 |
rs753156416 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923316 | GGCAGGGTACAAGAG[A/G]CAAGTGTGAGCCAGG | 55833 |
rs753168467 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963985 | TTGATGGCTCTTGGA[C/T]ACTCAAATCACTTCA | 55833 |
rs753170092 | snp | A/G | 1.69e-05 | 0.00290684 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927970 | GAGGACTGGTGGGAA[A/G]AGGCGCTCTCCACAC | 55833 |
rs753176086 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974506 | AGTGAGACCATTTCT[C/T]AAAAACAAACAAAAA | 55833 |
rs753178288 | in-del | -/AAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030451 | CAGATTCCATCTCAA[-/AAAC]AAACAAACAAACAAA | 55833 |
rs753186592 | snp | A/G | 1.65299e-05 | 0.00287483 | utr-variant-5-prime, stop-gained | UBAP2 | GRCh38.p7 | 9:33998852 | GAGCGAGACGCATCT[A/G]TTCAGCTGTTGCCTG | 55833 |
rs753209880 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020665 | TGGAACTCTGTTTCC[C/T]TTTTTTTTTTTTGAG | 55833 |
rs753235230 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008170 | AATACAAAATTAGCC[A/G]GGCCGGGCATGGTGG | 55833 |
rs753287356 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963811 | GGACCAATGTAAAAT[C/T]GAGGGTTTAAACATA | 55833 |
rs753330603 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970174 | CCTGAGCTCAAGCTG[A/T]GTTATCTTATAATCT | 55833 |
rs753331597 | snp | C/T | 1.81421e-05 | 0.00301176 | missense | UBAP2 | GRCh38.p7 | 9:33922695 | TACTCACCTGTGCAT[C/T]CTGCGGAAGGTGGTG | 55833 |
rs753391296 | snp | A/C | 1.69717e-05 | 0.002913 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971804 | AGAAGCAAACACCTA[A/C]GCCAAAATATTAACC | 55833 |
rs753439500 | snp | A/T | 3.29674e-05 | 0.00405988 | missense | UBAP2 | GRCh38.p7 | 9:33948425 | GCTTGAGGTCCCAAG[A/T]AGTAGTAGTTGTAGG | 55833 |
rs753447764 | snp | A/G | 3.62536e-05 | 0.0042574 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935734 | GGGCTGCTTTTTAAC[A/G]AATAAGCCATTGACC | 55833 |
rs753457101 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970978 | CGGCTAATTTTTTGT[A/G]TTTTTGTAGAGACAG | 55833 |
rs753472905 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026058 | GCATACAAAAAACAC[A/G]GTCGGGTAAAAACTT | 55833 |
rs753481732 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043299 | ACCTCAGCCTCCTGA[C/G]TAGCTGGGACTACAA | 55833 |
rs753485208 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935412 | GGGATTACAGGCACG[C/T]GCCGCCACCACACCC | 55833 |
rs753516283 | snp | C/T | 0.000432612 | 0.014701 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922786 | TGCATAGCCAGGGGC[C/T]GCTCCCGAGGCCAGG | 55833 |
rs753523901 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959686 | TAACATGCTCAAAAA[C/T]ATCTGTGCAATAAAG | 55833 |
rs753527202 | in-del | -/AAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974509 | GAGACCATTTCTCAA[-/AAAC]AAACAAAAAAACACC | 55833 |
rs753605230 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967728 | AGAAATGTCATCTCC[-/A]AAAACAAGTTAAAGG | 55833 |
rs753609465 | snp | C/G | 4.94393e-05 | 0.00497164 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935800 | TCCTCTGTTTGGTTG[C/G]CACCAGCCATGACAA | 55833 |
rs753654618 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022777 | TTTAAGAAAAGAATA[A/C]AACAGAATTAAGCAT | 55833 |
rs753664009 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | UBAP2 | GRCh38.p7 | 9:33923458 | GTTCACCCCATGTTG[C/G]TTGGCTGAGGCTGGA | 55833 |
rs753685312 | snp | A/G | 4.94425e-05 | 0.0049718 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989006 | CGCCTCTTCCTTTCC[A/G]GTTGTTGTTTCCACG | 55833 |
rs753700556 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931995 | TCTCACTACCATTCA[C/T]TCCGCAACCCACCAC | 55833 |
rs753713466 | in-del | -/ATAACATC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930428 | CTTAAATAACCTTAA[-/ATAACATC]ATAAAGCAGAACTGT | 55833 |
rs753737800 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993934 | GAGTCTCGCACTGTC[A/G]CCTGGGCTGGAGTGC | 55833 |
rs753752965 | snp | C/G | 1.66815e-05 | 0.00288799 | missense | UBAP2 | GRCh38.p7 | 9:33927031 | ACCTACGAGGTACTG[C/G]TTGTGCAGCAGGGGA | 55833 |
rs753764343 | in-del | -/TC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932699 | CAAGACGCACGTGGG[-/TC]AGTGAGCTAGATTCA | 55833 |
rs753789587 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004579 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55833 |
rs753789746 | snp | C/T | 1.66283e-05 | 0.00288338 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956182 | TTTAATCTTATTCTA[C/T]ATACTACTAAACCCA | 55833 |
rs753790475 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987466 | ATTATCCAGGTATGG[C/T]TGTGACAGCGTGCAG | 55833 |
rs753806180 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042054 | AACATGGATAAATCT[C/G]AAGCATGTAAGAGTG | 55833 |
rs753833083 | in-del | -/GCC | | | utr-variant-5-prime, intron-variant | UBAP2 | GRCh38.p7 | 9:34048856 | GACCCAAGACCCGCT[-/GCC]GCCGCCGCCGCCGCT | 55833 |
rs753835740 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020750 | CCGCAAGCTCTGCTT[C/T]CTGGGTTCACGCCAT | 55833 |
rs753849542 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017075 | TGTTTCTGTGGTTGC[A/G]TTGATTGTGCTGCTG | 55833 |
rs753850022 | snp | C/G | 4.94605e-05 | 0.0049727 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923518 | TTAGTGTAGGAAGAG[C/G]CAAGCTGAGGCTGGT | 55833 |
rs753861552 | snp | C/T | 0.000110589 | 0.0074352 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922401 | GGCATGGCTGACACA[C/T]GTCGGGAATTCTAGG | 55833 |
rs753868421 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033617 | GGGTCTGACTCTTTC[A/G]CCCAGGCTGAAGCGC | 55833 |
rs753897235 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966981 | AGTCAGTAAAAACTA[A/T]ATGTCACAACAGTGG | 55833 |
rs753902309 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956240 | CATCAGTAGTCTCTT[-/A]ACACTTCGCATAACA | 55833 |
rs753909816 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998156 | CCTGTAATCCCAGCA[C/T]TCTGGGAGGCCAAGG | 55833 |
rs753910699 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953154 | GATTACAGGCATGAG[C/G]CATCATGCCCGGCCT | 55833 |
rs753932228 | snp | A/G | 1.66768e-05 | 0.00288758 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944321 | GAGCTGAATGTAAAA[A/G]TAATTCCAGCTTTAG | 55833 |
rs753937561 | snp | A/G | 0.000119475 | 0.00772809 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017197 | TAGAAAATCTGCAAG[A/G]AAGTAGGGATGGTAA | 55833 |
rs753939529 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983981 | CAATGGTACAATCTC[A/G]GCTCACTGCAGCCTC | 55833 |
rs753943172 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996930 | AAAAAATTAACCGAG[C/T]GTAGTGGTAGGAGGA | 55833 |
rs753968920 | snp | C/G | | | missense | UBAP2 | GRCh38.p7 | 9:33922704 | GTGCATCCTGCGGAA[C/G]GTGGTGGTGCAGCAG | 55833 |
rs753991639 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924180 | GGCCGGCCCCGGGCT[A/G]CTCCTCATCCATTGA | 55833 |
rs753994440 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983682 | TCCCAAGGTGTGTAC[C/T]TCAGGGTTTAGGACC | 55833 |
rs754006766 | snp | A/C | 1.658e-05 | 0.00287919 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932570 | CACTTACTGTGTGTG[A/C]CGTGCTCGAGGAGAG | 55833 |
rs754023879 | snp | C/T | 4.55976e-05 | 0.00477459 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922491 | TGCCCCAGCCCACCC[C/T]TCTCTTCTGGGTTTA | 55833 |
rs754036385 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954113 | GGTTTCACCATGTTG[C/G]ACAGGCTGGTCTCAA | 55833 |
rs754037570 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965854 | GAGATGGAGACCATC[C/G]TGGCTAACACAGTGA | 55833 |
rs754051999 | snp | A/C | 9.89936e-05 | 0.0070347 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973265 | ACACAATTATAGTAT[A/C]AAATAATACTTATGT | 55833 |
rs754060823 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023603 | AAATAATGACCCGGT[C/T]GCATGGCTAAACCAG | 55833 |
rs754083202 | in-del | -/TTACT | 3.51309e-05 | 0.00419097 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941897 | TTCAACATAATTTTG[-/TTACT]TTAAATAGCTTCATA | 55833 |
rs754083725 | snp | A/G | 4.94222e-05 | 0.00497078 | missense | UBAP2 | GRCh38.p7 | 9:33924250 | TCTCGGCTGGCAAGC[A/G]CTGTGGGTGCAGCAA | 55833 |
rs754091846 | snp | C/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921940 | AAGACAAACAGGTGG[C/G]CATACTTGGGTGGAG | 55833 |
rs754129606 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003269 | CGTCTGACCTCGAGT[G/T]ATCTGCCCACCTTGG | 55833 |
rs754142197 | snp | A/T | 1.6476e-05 | 0.00287014 | missense | UBAP2 | GRCh38.p7 | 9:33948556 | ATTTTTGGTGGTGCA[A/T]GCTCTCCAAATCCTG | 55833 |
rs754217322 | snp | C/T | 1.73468e-05 | 0.00294501 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986735 | CCTAATTGAAAGCAT[C/T]TTCTTCCCTCTTACT | 55833 |
rs754226449 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942831 | ACATGTGGAGAAATT[A/G]GATCCCTCATAGACT | 55833 |
rs754259732 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961308 | CTGTCTTGGACCCTA[C/T]TTCAGGTGGATTACT | 55833 |
rs754290817 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929529 | GATTTCCTTTATGTA[C/T]TGATGGAGAGTGGTA | 55833 |
rs754312043 | in-del | -/AG | 1.81358e-05 | 0.00301124 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927763 | ACCTTTGAGGGGCTC[-/AG]GGGTGGGCAGGAAAG | 55833 |
rs754319819 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005435 | GCAAGACCCTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 55833 |
rs754343501 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045444 | GTCCAATGGCACATG[C/G]CTCACAGCAACCTCC | 55833 |
rs754355229 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | UBAP2 | GRCh38.p7 | 9:33941707 | TGGTATGGGATCCTG[C/T]TATGCACAGAACTCT | 55833 |
rs754369155 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017338 | GATTTTACATTTTGC[C/T]GGTATCTGTTAAACC | 55833 |
rs754373467 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012964 | AAAACTGACTAACCT[A/G]GCCAACATGGTGAAA | 55833 |
rs754396487 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928456 | CTTTTGGAGATTTCC[C/T]TTCTATTGGGATTCT | 55833 |
rs754436529 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974343 | AAACCTTGTCTCTAC[-/A]AAAAAATACAAATAT | 55833 |
rs754450072 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049768 | AGTCCAGGATTTTCC[C/G]TATTTAAGGATTTAA | 55833 |
rs754452303 | snp | C/T | 1.8529e-05 | 0.00304371 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944688 | ATGGCTTCACAATGT[C/T]CTTCAATAGAACATG | 55833 |
rs754504677 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036336 | TGGTCAGGATGGTCT[-/C]AAACTCCCGACCTCA | 55833 |
rs754506040 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969182 | CTATCAATCTTTTTG[C/T]ACAAGATTTTATGTG | 55833 |
rs754509360 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925970 | TCCCCTCTGTCCCCA[A/C]AGTTCTGTTCATGTG | 55833 |
rs754511757 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971007 | AGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 55833 |
rs754513277 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957226 | TAAACCATGAGTTTC[G/T]ATTATTTTTAAAAAA | 55833 |
rs754525759 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020148 | AGGGAGACTCCATTA[-/T]TTAAAAAAAAAAAAA | 55833 |
rs754526055 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980543 | ACCGCACCCGGCGAG[A/C]GTCATTTCTAATACA | 55833 |
rs754531113 | snp | C/T | 9.88957e-05 | 0.00703122 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924035 | CCAGCCACTGCCCTT[C/T]CTCCAACCAGAGAAA | 55833 |
rs754543713 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005435 | GCAAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs754551233 | snp | C/T | 1.80156e-05 | 0.00300124 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922789 | ATAGCCAGGGGCCGC[C/T]CCCGAGGCCAGGGGC | 55833 |
rs754573211 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012978 | TGGCCAACATGGTGA[A/T]ACCCCTCTCTACTAA | 55833 |
rs754577964 | in-del | -/GAG | 0.000448845 | 0.014974 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922608 | AGCCACTCTGAGGAA[-/GAG]GAGAAGGGAAGGCTG | 55833 |
rs754579146 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990139 | AAAATTATCAAGCAG[A/G]GTAGTTACAGAGAAA | 55833 |
rs754661853 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027381 | AGCAAATCGGGAGGC[C/T]GAGGCAGGAGAATCC | 55833 |
rs754667078 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932053 | CCATGCTCACGGCTC[C/T]ACGACCCACTGAGCC | 55833 |
rs754686127 | snp | A/G | 3.29609e-05 | 0.00405948 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989007 | GCCTCTTCCTTTCCG[A/G]TTGTTGTTTCCACGT | 55833 |
rs754708465 | in-del | -/AAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930455 | GCAGAACTGTGGGGA[-/AAC]AACAACAACAACAAC | 55833 |
rs754739728 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946891 | ATAGGGACCTACAAT[G/T]CCTCTCAAAAAGGCC | 55833 |
rs754756273 | snp | C/T | 1.6489e-05 | 0.00287128 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989077 | TCTTTGTTTTCTGAA[C/T]TTTCTTTTGCAAAAT | 55833 |
rs754771877 | snp | C/T | 1.70702e-05 | 0.00292144 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953512 | GGAACCAGTCATAAG[C/T]AAATCTTACCAACAA | 55833 |
rs754811339 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923461 | CACCCCATGTTGCTT[A/G]GCTGAGGCTGGAGGG | 55833 |
rs754831240 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023667 | GCTTACTTTATTGTT[C/T]GGAAAAAGTTTTTCT | 55833 |
rs754831279 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008187 | GCCGGGCATGGTGGC[G/T]CATGCCTGTAATCCC | 55833 |
rs754847455 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033642 | AAGCGCAGTGGTGCA[A/C]TCTCGGTTCCCTGCA | 55833 |
rs754885019 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033712 | CCTCCCAAGCAGCTG[C/T]GACTACAGTCAAGCA | 55833 |
rs754898989 | in-del | -/AGTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969434 | TGCCATAGTTCCAGC[-/AGTA]AGTACTAGGGAGATT | 55833 |
rs754920579 | snp | A/G | 8.23961e-05 | 0.00641804 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943512 | AGAAGGTTCTGACCC[A/G]AATTCCAGAGCCCCA | 55833 |
rs754923339 | snp | C/T | 3.29533e-05 | 0.00405901 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:34017080 | CTGTGGTTGCGTTGA[C/T]TGTGCTGCTGAAATC | 55833 |
rs754924152 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958163 | GACAGGGCCTCCCTA[C/T]GTTGCCCAGGCTGCA | 55833 |
rs754931865 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945522 | AAAAACAAAATCCAA[C/T]AGATACAAGAATATG | 55833 |
rs754936572 | snp | A/G | 1.66715e-05 | 0.00288712 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956188 | CTTATTCTACATACT[A/G]CTAAACCCAAAACAC | 55833 |
rs754977003 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33973186 | GCTATCACTTACCCC[A/G]TGCCTTGGGTTGAGA | 55833 |
rs754979730 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951635 | AACAGGTGTGAGCCA[C/T]CGCGCCCAGCTCCCA | 55833 |
rs754983146 | snp | C/T | 2.24323e-05 | 0.00334898 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922492 | GCCCCAGCCCACCCC[C/T]CTCTTCTGGGTTTAG | 55833 |
rs754997412 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954134 | CTGGTCTCAAACTCC[C/T]GCTCTCAAGTGAGCT | 55833 |
rs754999023 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047227 | AATCTCTCGTCACAC[C/G]TATCAACTAGCCATA | 55833 |
rs755024364 | snp | G/T | 1.66729e-05 | 0.00288724 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944326 | GAATGTAAAAATAAT[G/T]CCAGCTTTAGGACGG | 55833 |
rs755083012 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924188 | CCGGGCTACTCCTCA[C/T]CCATTGAGCAAACTC | 55833 |
rs755118157 | in-del | -/ACAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945492 | GTGACAGACTGGGTG[-/ACAA]ACAAACAAACAAAAA | 55833 |
rs755139390 | in-del | -/AAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936666 | AAAACAAAACAAAAC[-/AAAT]AAATAAATAAAGGAG | 55833 |
rs755151162 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997031 | AGCGAGACCCTGTCT[-/C]CCCCCCTCAAAAAAA | 55833 |
rs755154312 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957470 | GACACTACAGATTAG[A/G]CTGCATTTTCTAGAA | 55833 |
rs755205149 | snp | A/C | 1.65048e-05 | 0.00287265 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973274 | TAGTATAAAATAATA[A/C]TTATGTCCTACACAA | 55833 |
rs755207224 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959778 | AGCAAACTTATTCAG[A/G]TTAATTTCAACTGTG | 55833 |
rs755240648 | snp | A/C | 1.85129e-05 | 0.00304238 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953254 | ATGGGTATATTTCTT[A/C]AAATCCCACACTGAA | 55833 |
rs755246168 | snp | C/T | 1.66142e-05 | 0.00288216 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922919 | AAGGTCAGGTTGGGC[C/T]GTAACCTCTCAAAAA | 55833 |
rs755278438 | snp | A/G | 1.64743e-05 | 0.00287 | missense | UBAP2 | GRCh38.p7 | 9:33924253 | CGGCTGGCAAGCGCT[A/G]TGGGTGCAGCAAAGG | 55833 |
rs755295090 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | UBAP2 | GRCh38.p7 | 9:33948558 | TTTTGGTGGTGCAAG[C/G]TCTCCAAATCCTGAG | 55833 |
rs755325223 | snp | C/T | 3.32099e-05 | 0.00407478 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941641 | AAAAAAACTAAAATA[C/T]CACTTACCATGATGG | 55833 |
rs755334221 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923056 | GAAAAGCAGTTGTTC[C/T]CCACAGCAGTTGTTC | 55833 |
rs755390513 | in-del | -/G | 1.81168e-05 | 0.00300966 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927764 | CCTTTGAGGGGCTCA[-/G]GGGTGGGCAGGAAAG | 55833 |
rs755394237 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929647 | ACTTCCCATCACCAA[A/G]GGCTCCCTAATATAG | 55833 |
rs755408434 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945432 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55833 |
rs755412710 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942727 | GCAAGACCCTATCTC[-/AAA]AAAAAAAAAAAAAAG | 55833 |
rs755414991 | snp | A/C | 3.29495e-05 | 0.00405877 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941715 | GATCCTGTTATGCAC[A/C]GAACTCTGGTCATAA | 55833 |
rs755419077 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990226 | AAGGGACTGGAAATG[A/G]CTCCATCCAAAATTA | 55833 |
rs755421894 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972590 | ATGGCTTCCACAGGA[C/T]GTTTTAAAACTCTTC | 55833 |
rs755428513 | snp | A/G | 1.64787e-05 | 0.00287038 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33996250 | CCCTTCCAGCAATAT[A/G]TTGATAGCTTTGTTC | 55833 |
rs755486623 | in-del | -/ACA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029506 | GGCACTCCAGCCTGG[-/ACA]ACAAGAGCAAAACTT | 55833 |
rs755497018 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017382 | CAATCTAAGTCTATG[A/G]TTTACGAGCTTAGCA | 55833 |
rs755509857 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005436 | CAAGACCCTGTCTCA[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs755512659 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974165 | ACTGTATGCAAGCCT[A/G]GGTGACATAGCAAGA | 55833 |
rs755514456 | snp | A/G | 4.98542e-05 | 0.00499245 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998761 | ATAGATTATAAAAAT[A/G]ATGATATCCTTTGCC | 55833 |
rs755554859 | in-del | -/TCTG | 1.64931e-05 | 0.00287163 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923356 | CTAACCCCATGTGTC[-/TCTG]TCTGGGAAGTACCCC | 55833 |
rs755576664 | snp | C/T | 3.29826e-05 | 0.00406082 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963795 | TTGATGCCAGTTCTG[C/T]GGACCAATGTAAAAT | 55833 |
rs755576935 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998401 | GACCACGTCTCTATG[-/A]AAAAAAAAATTTTTT | 55833 |
rs755579665 | snp | A/G | 1.71026e-05 | 0.00292421 | missense | UBAP2 | GRCh38.p7 | 9:33927811 | CCTGAGGTCACCAAG[A/G]GCGCGGCCCTGCTAC | 55833 |
rs755584293 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935002 | CGCACTCCCAGGAAA[C/T]CCTATTTAAAGAGTC | 55833 |
rs755586638 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | UBAP2 | GRCh38.p7 | 9:33923940 | CTCTGCTGTGGCTGA[A/G]CTGGTGTGGTAGCGG | 55833 |
rs755620173 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968768 | CAATTTGTGCAATCA[A/T]CACCTCTAATTCTAG | 55833 |
rs755634191 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013270 | AAAGAACTCTCACCA[C/T]CTGCTGCAGTGGCTC | 55833 |
rs755634623 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | UBAP2 | GRCh38.p7 | 9:33923854 | AGTAGGGAAGACCAG[C/T]GTAGCTATAGCCAGG | 55833 |
rs755644818 | in-del | -/G | 0.000267188 | 0.0115552 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017015 | ATAAAAGAAAAAAAA[-/G]GGAAAAAAAAAAAAA | 55833 |
rs755650960 | snp | A/G | 1.73474e-05 | 0.00294506 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922611 | CACTCTGAGGAAGAG[A/G]AGAAGGGAAGGCTGT | 55833 |
rs755658031 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980141 | AACACATACTTAGCT[A/G]ACATTCTAATAATTC | 55833 |
rs755676471 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029683 | TCTATTTAAAAAAAT[-/AAA]AAGAAGAAGAAGGAA | 55833 |
rs755677865 | snp | A/T | 3.62273e-05 | 0.00425586 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922683 | CCTCCATCACTGTAC[A/T]CACCTGTGCATCCTG | 55833 |
rs755721875 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962282 | TACAGTTAATGTAGT[A/G]AGTTAAAACAGACTT | 55833 |
rs755728909 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011822 | ATCACTACAGCTCTT[-/C]CTCTGGATCTCTTAC | 55833 |
rs755749229 | in-del | -/TA | 1.71855e-05 | 0.00293129 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948364 | AACCCACAAACAATG[-/TA]TATACCTACCAAGAT | 55833 |
rs755764279 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991712 | CACTGAACAAACTCA[A/G]TTTATTATGTTTGCT | 55833 |
rs755788272 | snp | C/G | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933596 | GGGAGCTCACAGACG[C/G]GAGGGCAGAGGGAGG | 55833 |
rs755806915 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926581 | CATGTAAAAGATTCT[A/G]AACCCTCTGCTCCGA | 55833 |
rs755824123 | snp | A/G | 3.58301e-05 | 0.00423247 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944676 | TAATGAGGCATAATG[A/G]CTTCACAATGTTCTT | 55833 |
rs755844777 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018607 | GGTCACTCACGCCTG[C/T]AATCCCAGCACTTTG | 55833 |
rs755845627 | snp | A/C | 3.29511e-05 | 0.00405887 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944383 | AGAAGCTGGGGGTAT[A/C]CGCCGCTTAGCAAGT | 55833 |
rs755860234 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969552 | AGATGCTCTCTCTTT[-/AAA]AAAAAAAAAAGAAAG | 55833 |
rs755860888 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981164 | ATATATATATTCTGG[-/AT]ATATATATATATATT | 55833 |
rs755890547 | in-del | -/CCTC | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050054 | GGCGGGTGGCCCCTT[-/CCTC]CCGCACCTCTCCATG | 55833 |
rs755891877 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979443 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTTATCC | 55833 |
rs755935139 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945412 | GCTGAGGCAGGCCCT[A/G]TGACGTGAACCCGGG | 55833 |
rs755935316 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930973 | GTGTTTTGACTTTTA[C/T]TTATTAAAAGGATGG | 55833 |
rs755936490 | snp | C/G | 1.65168e-05 | 0.00287369 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986875 | ATCAAATTTCCATTT[C/G]CAAACCTCTTGTACA | 55833 |
rs755936538 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032501 | TTCCCCCTTTGGCCA[A/G]TCAGAAGGAAGGAAG | 55833 |
rs755950597 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039374 | CTGCTCATTGAGAAC[-/G]GGGCCATGATGACGA | 55833 |
rs755968226 | snp | C/T | 1.65111e-05 | 0.0028732 | missense | UBAP2 | GRCh38.p7 | 9:33926658 | GGAGCTCGTCATAGC[C/T]ATAGATCTGTGTGAG | 55833 |
rs755970626 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987336 | AGAATTGCTTGGACC[C/G]AACAGGCGGAGGTTG | 55833 |
rs755975591 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021305 | TGTACTGCCTTTTAC[A/G]TTATAGTAACAACCA | 55833 |
rs755987210 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049657 | GGTTTTACTTTTGCC[C/T]TCCCAAGCCCCTTCT | 55833 |
rs756025777 | in-del | -/TCTGGGATGTGGGGAGCGCCTCTGCCCCGCCACCCCA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038901 | TGCCCCGCCACCCCG[lengthTooLong]TCTGGGATGTGAGGA | 55833 |
rs756035866 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955344 | GCCAATATGGTGAAA[C/T]CCCGTCTCCACTAAA | 55833 |
rs756037413 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014079 | TGTAATCCCAACACC[A/T]TGGGAGATCAAGGGG | 55833 |
rs756040109 | in-del | -/GCAGGAGCCCA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923133 | CTGAGAGGGGATCAG[-/GCAGGAGCCCA]GCAGGAGCCCACCAC | 55833 |
rs756056763 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985668 | AGGCAGAGAAGGTGA[G/T]GGGTATAGAGGGTGG | 55833 |
rs756060378 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953418 | GTTTCAAAGGAGTTG[A/G]CTTCTGAGGCTTGAC | 55833 |
rs756075342 | snp | A/G | 0.000152051 | 0.00871795 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953503 | AAGCAATGAGGAACC[A/G]GTCATAAGCAAATCT | 55833 |
rs756078754 | snp | A/T | 3.29538e-05 | 0.00405904 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943473 | ACTATTTTCACTGCT[A/T]GGAGCTGATCCAAAT | 55833 |
rs756090991 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000528 | ATCATCTCTGTACAA[C/T]GGTCTATTAAATCTA | 55833 |
rs756106193 | snp | A/C | 1.66164e-05 | 0.00288235 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998898 | TGTTAAGGATTTGAA[A/C]ACCAAAAGCATAAGT | 55833 |
rs756130568 | snp | A/G | 1.66369e-05 | 0.00288412 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941877 | ACTGAAAAGAGTCAA[A/G]AATATTCAACATAAT | 55833 |
rs756171645 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995881 | AGATGTAAGAAGTAA[C/T]CAGAGGTGAGGACTG | 55833 |
rs756204910 | snp | A/C | 1.74912e-05 | 0.00295725 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927989 | CGCTCTCCACACTGG[A/C]ATGCTGGCAAAAGAA | 55833 |
rs756242174 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951935 | TTTTTATTAGGCCTT[C/T]TCAAAATAGAGAAGC | 55833 |
rs756242195 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965589 | GTTTCATGTTTAAGT[A/G]TAACCTTGGAGGGTA | 55833 |
rs756249600 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962127 | ACATACACACACAGG[G/T]ATATAAAGGAAAATT | 55833 |
rs756250199 | in-del | -/ATAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945675 | GACAGACAGACAGAC[-/ATAT]ATATATATACACACA | 55833 |
rs756256310 | snp | C/T | 6.58892e-05 | 0.00573936 | missense | UBAP2 | GRCh38.p7 | 9:33923445 | TGGGAGTGCTGAGGT[C/T]CACCCCATGTTGCTT | 55833 |
rs756288686 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936377 | TAGATCACTGCAAAC[A/T]CCATCTCCCAGGTTC | 55833 |
rs756303532 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951158 | ATTACAGTAGCTATG[-/AT]TACAGGGCATGTGCC | 55833 |
rs756306089 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976295 | ATTCATACAACATTA[C/T]ATTATATTGCCATAA | 55833 |
rs756313550 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975303 | CAGGCGTGGTGGCGC[A/G]CGCCAGTAGTCTCAG | 55833 |
rs756352711 | in-del | -/GT | 1.64727e-05 | 0.00286986 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33923283 | TGTCCCCTGGGTCAG[-/GT]CGTCATAACCTAGCG | 55833 |
rs756366558 | snp | C/T | 6.63251e-05 | 0.00575831 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932564 | CGCAGACACTTACTG[C/T]GTGTGACGTGCTCGA | 55833 |
rs756367911 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941414 | AAAGTGCTCATACTA[C/G]ACGCATGCTTGGTTT | 55833 |
rs756388283 | snp | A/G | 1.6492e-05 | 0.00287154 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973254 | TTTAAAAAAACACAC[A/G]ATTATAGTATAAAAT | 55833 |
rs756391204 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022737 | GCCATCATGCCCAGC[A/C]ACCTATCTCCTTAAA | 55833 |
rs756435412 | snp | C/G | 5.00923e-05 | 0.00500436 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922912 | AATGGTGAAGGTCAG[C/G]TTGGGCTGTAACCTC | 55833 |
rs756447577 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017201 | AAATCTGCAAGAAAG[G/T]AGGGATGGTAAGCAA | 55833 |
rs756456490 | snp | A/G | 3.29603e-05 | 0.00405944 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924177 | CTAGGCCGGCCCCGG[A/G]CTACTCCTCATCCAT | 55833 |
rs756473705 | in-del | -/TTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021633 | AAAGAATCCATTTGA[-/TTTT]TTTTTTTTTTTTTTT | 55833 |
rs756486152 | snp | A/C | 1.7953e-05 | 0.00299603 | missense | UBAP2 | GRCh38.p7 | 9:33922817 | GGCCCAGTGGAGCCC[A/C]AGACCGAGGGCAGGC | 55833 |
rs756513939 | in-del | -/T | 3.44341e-05 | 0.0041492 | splice-acceptor-variant | UBAP2 | GRCh38.p7 | 9:33922600 | TGACCCGAGCCACTC[-/T]TGAGGAAGAGGAGAA | 55833 |
rs756531438 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982630 | CCATACAGTCCCAGT[A/G]AGAATAGGAAGAACA | 55833 |
rs756535175 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021696 | TGGAGTGCAGTGATG[G/T]GATCTCAGCTCACTG | 55833 |
rs756569472 | in-del | -/GGAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992656 | GACAACTTATCGGGC[-/GGAG]GGGGGGGGGCACAAA | 55833 |
rs756617740 | snp | G/T | 3.37365e-05 | 0.00410696 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989126 | CAGTCTCCCATGAAG[G/T]CTATCAGAGAGAACG | 55833 |
rs756624361 | in-del | -/CAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994755 | AATTACTGCTACACT[-/CAAA]CAGTGAAATCTTTTC | 55833 |
rs756628455 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010763 | GGAGCTACAACAAAC[A/G]TTTTTTTTTAAAAAG | 55833 |
rs756633364 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028540 | ACCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 55833 |
rs756649159 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953086 | TTTTGCCCAGTCTGG[C/T]TTCAAACTCCTGGGT | 55833 |
rs756663190 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935848 | ACTTACTGTCTAGTG[C/T]CTGCTGACTTCGACC | 55833 |
rs756686638 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015602 | AAAGTGCTGGAATTA[C/T]AGGCATGAGCCACTG | 55833 |
rs756705755 | snp | A/G | 1.64912e-05 | 0.00287147 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996230 | ATACTTACTGTGTCT[A/G]AATTCCCTTCCAGCA | 55833 |
rs756726407 | in-del | -/AG | 1.64727e-05 | 0.00286986 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33944434 | CTGGTGGACAGACAC[-/AG]AGATATTTTCAATGG | 55833 |
rs756732359 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948877 | GATGTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 55833 |
rs756745564 | snp | A/T | 1.76229e-05 | 0.00296835 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927791 | AAAGGCCTCTGGAGC[A/T]AATACCTGAGGTCAC | 55833 |
rs756749147 | snp | C/T | 1.74433e-05 | 0.0029532 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941611 | AATTTCCAAATAAGA[C/T]GGACATCTTCTGAGA | 55833 |
rs756769413 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933073 | GCCACCCATTTTCCT[A/G]CACCTTGTTCTAATA | 55833 |
rs756775292 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010899 | TATGTCAGAGTAGAA[G/T]ATAAACCAAAGTCAG | 55833 |
rs756822268 | snp | C/T | 4.95332e-05 | 0.00497636 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923768 | CCCAAGGCCAGGAGA[C/T]ACAGTCACACCCTCT | 55833 |
rs756823606 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926216 | AGACCAAAGACACTA[C/T]ATGGTACTCTGAGGA | 55833 |
rs756879363 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031328 | GCAAAACCCCGTCTC[C/T]ACTGAAAATACAAAT | 55833 |
rs756884889 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035859 | TGCCTTCACGTTCCA[C/T]AGGCATGTTTACTCA | 55833 |
rs756889587 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002864 | TGGTTAATGTTTTGT[C/T]TTTAGTACAAACAAG | 55833 |
rs756908973 | snp | A/G | 4.94205e-05 | 0.0049707 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923843 | CATGCCTGTGTAGTA[A/G]GGAAGACCAGTGTAG | 55833 |
rs756917696 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046646 | AAGACTCCATCTCAA[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 55833 |
rs756925296 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947259 | GGAATATGCTTCCCT[A/G]TCTCTCTATATGCCC | 55833 |
rs756950516 | snp | G/T | 7.23079e-05 | 0.00601238 | missense | UBAP2 | GRCh38.p7 | 9:33922517 | GTTTAGTTTGTCCAG[G/T]ATGGAGAGTTGCCGT | 55833 |
rs756973207 | snp | C/T | 1.64876e-05 | 0.00287116 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963779 | GCTATGTTGTGAGTA[C/T]TTGATGCCAGTTCTG | 55833 |
rs757020874 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989941 | GGGTTTTTAAAAAAT[G/T]TATAAAGCACCTAAA | 55833 |
rs757022773 | snp | A/G | 1.6477e-05 | 0.00287024 | stop-gained | UBAP2 | GRCh38.p7 | 9:33944514 | CAGGTGTTGATTCTC[A/G]AAGTTTTGCCTGGGA | 55833 |
rs757038458 | snp | C/T | 1.71953e-05 | 0.00293212 | missense | UBAP2 | GRCh38.p7 | 9:33922598 | CGCTGACCCGAGCCA[C/T]TCTGAGGAAGAGGAG | 55833 |
rs757094326 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933571 | GCAGTGCAGGAGGTG[A/G]TGCTGGGCAGGGAGC | 55833 |
rs757124778 | snp | A/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049530 | TGGGGTTCCGCTCCC[A/T]CGTTCCTGGGCTCGC | 55833 |
rs757137932 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012260 | TTACAGCTGGGCCCA[C/G]TGGCTCATGCTTGTA | 55833 |
rs757151465 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | UBAP2 | GRCh38.p7 | 9:33924268 | GTGGGTGCAGCAAAG[A/G]GAATTCCATAGTAGT | 55833 |
rs757163830 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967280 | ATCACAAAAAACAAC[A/G]GTTTATTCTCCCTTT | 55833 |
rs757205449 | snp | A/G | 1.65034e-05 | 0.00287253 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986855 | AGGGGGAAAAGAGCA[A/G]AAAAATCAAATTTCC | 55833 |
rs757208280 | in-del | -/GTG | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049252 | TGCTCATCACGTGAT[-/GTG]GTCCAACCACTCAGG | 55833 |
rs757231806 | in-del | -/CT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951893 | CGGAGGAGGAAAAGA[-/CT]CTGGTGCGTCAATTA | 55833 |
rs757236418 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013078 | AGAATCACTTGAACC[A/C]AGGAGGCACAGTTGC | 55833 |
rs757249029 | snp | A/T | 1.6591e-05 | 0.00288015 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953305 | TCTGAGGAGAACAGG[A/T]GTTGACGGCAGTGGA | 55833 |
rs757254967 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945053 | GAGGATTGCTTTAGC[A/C]CAGGAGTACAAGGCT | 55833 |
rs757256497 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962552 | TGAGGAGGCTGAGGC[A/G]GGAGAATCGTTTGAA | 55833 |
rs757276851 | in-del | -/A | 3.29712e-05 | 0.00406011 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923158 | ACCACTCCAGGCCTT[-/A]ATCCTGGAAAGGAGA | 55833 |
rs757284104 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935166 | GTTGGAAGTGGCGGG[-/GGG]GGGGGGGGGTCTCAT | 55833 |
rs757348396 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041814 | AGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 55833 |
rs757352833 | snp | A/G | 1.65924e-05 | 0.00288027 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941872 | GGCTCACTGAAAAGA[A/G]TCAAAAATATTCAAC | 55833 |
rs757359696 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003264 | TTGAACGTCTGACCT[C/T]GAGTGATCTGCCCAC | 55833 |
rs757381965 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976181 | AAAACTTTCAGTCTA[C/T]AGCTTTTGGCAAGAA | 55833 |
rs757392734 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990059 | AATCTAATCTACCAT[-/AT]ATATATATATATAAA | 55833 |
rs757395958 | snp | A/G | 1.6504e-05 | 0.00287258 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33926650 | CAGCATCTGGAGCTC[A/G]TCATAGCCATAGATC | 55833 |
rs757410949 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032357 | ACTCAGGCATATTTC[C/T]GTCTTTATACACTCA | 55833 |
rs757416452 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923334 | AGTGTGAGCCAGGCA[A/G]GCCTGTCTAACCCCA | 55833 |
rs757432312 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956884 | ACACTCTGGGCAGCC[A/G]AGGCAGGAGGATTGC | 55833 |
rs757461767 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021137 | AACCATAATTCATCA[C/T]ACTAATTCAGGTACC | 55833 |
rs757492990 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019513 | ACCAGAGGCTGGGGG[A/T]AGGGGAAGAATGGGG | 55833 |
rs757502923 | snp | A/G | 1.72722e-05 | 0.00293867 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927984 | AGAGGCGCTCTCCAC[A/G]CTGGCATGCTGGCAA | 55833 |
rs757509449 | in-del | -/T | 0.000103146 | 0.00718069 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922410 | GACACATGTCGGGAA[-/T]TCTAGGAAAGGGCAC | 55833 |
rs757515948 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | UBAP2 | GRCh38.p7 | 9:33943465 | ATCTGATTACTATTT[C/T]CACTGCTTGGAGCTG | 55833 |
rs757522314 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002379 | CACTGCATAGGTGCT[-/TTT]TTTTTTTTTTTTTTT | 55833 |
rs757529899 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982618 | TATGAACAGCCACCA[C/T]ACAGTCCCAGTAAGA | 55833 |
rs757537452 | snp | C/T | 1.65162e-05 | 0.00287365 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998798 | ATACCTGCTTAACTT[C/T]AGCTTCAAAATCTGA | 55833 |
rs757553798 | snp | C/T | 1.65712e-05 | 0.00287843 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998877 | TGCCTGGAAAGTACA[C/T]ACAATTGTTAAGGAT | 55833 |
rs757591427 | snp | A/G/T | 4.94534e-05 | 0.00497239 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924040 | CACTGCCCTTCCTCC[A/G/T]ACCAGAGAAAGGCCA | 55833 |
rs757592101 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023530 | ATCAACATTAAGACT[A/G]TATCTCCTTCCAATC | 55833 |
rs757612375 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047382 | CAGGTGAGTGTATTG[A/C]AGGAAACTATCATCT | 55833 |
rs757613229 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974680 | GCAACGGCCAGGCCC[A/G]GTGGCTCATGCCTGT | 55833 |
rs757623615 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972242 | AATAAAATCCTAAAC[C/T]GAACACCCAGTTTAA | 55833 |
rs757630388 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | UBAP2 | GRCh38.p7 | 9:33923970 | GGTGCAGGGGATGCA[A/G]AGTCCCCACGGCCAA | 55833 |
rs757634859 | in-del | -/TAGACA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997140 | CACAAAACACACTCC[-/TAGACA]TATTTTCTCAAGGAT | 55833 |
rs757645965 | snp | A/T | 1.6489e-05 | 0.00287128 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017057 | AAACTTACCTGTACC[A/T]CTTGTTTCTGTGGTT | 55833 |
rs757646025 | snp | A/C/T | 8.24091e-05 | 0.00641864 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971738 | TAGAATCTGAATAGT[A/C/T]TGCAGGATTAAATGT | 55833 |
rs757663042 | in-del | -/A | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952559 | CGCCTAGGCAGACTC[-/A]AGACTGTTTTTACAT | 55833 |
rs757679105 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950401 | ATATCCATTTAAGGT[C/G]AAAAACAAATACTTT | 55833 |
rs757692633 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993530 | AAAAATGATTAGCCA[A/T]GCGTAGTGGCATGCG | 55833 |
rs757694545 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007600 | CATACATTTTTCAGC[A/G]TTTATTGAAATGATC | 55833 |
rs757713620 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014421 | GTCACTTGGGCTCAG[C/G]TGTTGGAGACCAGGC | 55833 |
rs757792179 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956318 | TTCAAGTGAATGCAA[-/TTT]TTTTTTTTTTTTTTT | 55833 |
rs757805140 | snp | A/G | 1.6495e-05 | 0.0028718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973144 | AGAATAAAAACTAGG[A/G]AAGTAAATAATTATA | 55833 |
rs757818997 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994964 | GTTTGTTTTAAATTT[C/T]CCAAGGAAAGGTAGT | 55833 |
rs757838877 | snp | A/T | 1.64768e-05 | 0.00287021 | missense | UBAP2 | GRCh38.p7 | 9:33948442 | GTAGTAGTTGTAGGG[A/T]GACTTGTACTATTCT | 55833 |
rs757869943 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935820 | AGCCATGACAAGAGT[A/G]GCTTGCTGCTATACT | 55833 |
rs757881460 | snp | A/T | 0.000140795 | 0.00838916 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938892 | TATAGACTCTAACTT[A/T]TTTCTGTCAAAGCAT | 55833 |
rs757882261 | snp | C/T | 0.0002636 | 0.0114774 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989020 | CGGTTGTTGTTTCCA[C/T]GTCCACGACTCGATT | 55833 |
rs757895907 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989437 | CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTT | 55833 |
rs757923109 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986849 | CTAACTAGGGGGAAA[A/G]GAGCAGAAAAATCAA | 55833 |
rs757936725 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971208 | TAAATAATCCAGAAA[A/C]AGCATGATACAGAAA | 55833 |
rs757955629 | snp | C/G | 3.295e-05 | 0.00405881 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989032 | CCACGTCCACGACTC[C/G]ATTCTTTCTCGCTTT | 55833 |
rs757961384 | snp | A/G | 1.67315e-05 | 0.00289231 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33989112 | TTTCTTACACCCTAC[A/G]GTCTCCCATGAAGTC | 55833 |
rs758012668 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013486 | ACAAGAGCAAAACTC[C/T]GTCTCAAAAAATAAA | 55833 |
rs758017951 | in-del | -/ATCT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968707 | TACACATAACATGAA[-/ATCT]ATCCTTTTACAACAG | 55833 |
rs758034285 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963214 | AGTCAGGAAATTACA[A/G]GGGAAACTCCCATGT | 55833 |
rs758039396 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951492 | GCTGGGATTATAGGC[A/G]CCCACCACTACGCCT | 55833 |
rs758053226 | snp | C/T | 1.67346e-05 | 0.00289258 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956196 | ACATACTACTAAACC[C/T]AAAACACTGACTTCC | 55833 |
rs758061328 | snp | A/C | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922161 | CTTCCAGAGACTGCC[A/C]CTAGTGGCCCACTGG | 55833 |
rs758068364 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928911 | GCAGACTAACTCTCC[A/G]CCGCCATCCCATGCC | 55833 |
rs758091077 | snp | C/T | 0.000101168 | 0.00711154 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927049 | GTGCAGCAGGGGAGG[C/T]ACCCCCTGAGGTAAG | 55833 |
rs758094280 | in-del | -/C | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050943 | TGGGTCGAGATCGCG[-/C]CCACTGCACTCCAGC | 55833 |
rs758099156 | snp | A/C | 1.68997e-05 | 0.00290682 | missense | UBAP2 | GRCh38.p7 | 9:33927051 | GCAGCAGGGGAGGCA[A/C]CCCCTGAGGTAAGTT | 55833 |
rs758102012 | in-del | -/AAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930897 | TGAGACTGCATCTCA[-/AAAAAAAAAA]AAAAAAAAAAAAGCG | 55833 |
rs758122415 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015412 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 55833 |
rs758139546 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972256 | CTGAACACCCAGTTT[A/T]ATCGAATCATGGTTC | 55833 |
rs758141548 | snp | G/T | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33933928 | ACACCTAAAGGAACC[G/T]AAGCTGTAGATGCAT | 55833 |
rs758151636 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33960870 | CTTCCACAGAATTCT[C/T]CCAAGCCCCTGTTGG | 55833 |
rs758187078 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923755 | CACCTGCCAGCAACC[C/T]AAGGCCAGGAGACAC | 55833 |
rs758208102 | snp | A/G | 3.31807e-05 | 0.00407299 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944340 | TTCCAGCTTTAGGAC[A/G]GTGACTTCATGATGA | 55833 |
rs758227401 | snp | C/T | 0.000102445 | 0.00715627 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922498 | GCCCACCCCTCTCTT[C/T]TGGGTTTAGTTTGTC | 55833 |
rs758235479 | snp | C/T | 1.6495e-05 | 0.0028718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922941 | TCTCAAAAACCTATA[C/T]ACCCAACCCACCTTT | 55833 |
rs758340754 | in-del | -/CAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015759 | GCTGGAGTGCAGTAG[-/CAT]CATCATAAGTGATCC | 55833 |
rs758376939 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947116 | TGTAGGCACAGGGTA[A/C]CTACATTTCTTGCCC | 55833 |
rs758377808 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973468 | CTTGTATTATATTTG[C/T]GGTATTTGACAGCTA | 55833 |
rs758393881 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966080 | CAGGGAGTGTGGGTC[G/T]TAGAACTTTTTTTTC | 55833 |
rs758399113 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | UBAP2 | GRCh38.p7 | 9:33924259 | GCAAGCGCTGTGGGT[A/G]CAGCAAAGGGAATTC | 55833 |
rs758427082 | in-del | -/AAA | 0.00439649 | 0.0466789 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017018 | AAAAGAAAAAAAAGG[-/AAA]AAAAAAAAAAGAGTT | 55833 |
rs758453743 | snp | C/T | 1.81741e-05 | 0.00301441 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932673 | CACCTGAACAAGTGA[C/T]TCCAGATGAACAAGA | 55833 |
rs758454488 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020149 | AGGGAGACTCCATTA[-/T]TAAAAAAAAAAAAAA | 55833 |
rs758488609 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928913 | AGACTAACTCTCCGC[C/T]GCCATCCCATGCCCA | 55833 |
rs758512238 | snp | C/T | 0.000347059 | 0.0131685 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924322 | GATCAGCGACTGGCC[C/T]TGCTTGACTCCCAGG | 55833 |
rs758519404 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985485 | TGGAATACTACTCAG[A/C]CATAAAAGAATGAAA | 55833 |
rs758565544 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979271 | TTCACTACCTTACTT[A/G]ACTCAATCTCACCAA | 55833 |
rs758579536 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929739 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55833 |
rs758587383 | snp | C/T | 1.68522e-05 | 0.00290272 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953285 | ATAAAAGTGAGTTAC[C/T]AGGCTCTGAGGAGAA | 55833 |
rs758602642 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954544 | AATCCTTTCAAAGGC[C/T]AGTTCCCATCAGTTC | 55833 |
rs758624471 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998287 | TCTGTCGTCATAGCT[A/G]CTCAGGAGACCGAGG | 55833 |
rs758626240 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982312 | ATGAAAGATATACTC[-/T]ATAGGAATGATTTTT | 55833 |
rs758628225 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936643 | GCAACACTCCATCTC[-/A]AAAAAACAAAACAAA | 55833 |
rs758630357 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938852 | TTCACATGGTTTTTC[-/T]TGTTTCAGTGCCCAT | 55833 |
rs758633820 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | UBAP2 | GRCh38.p7 | 9:33941833 | TTCTGTACTGCACTG[A/G]TCATTGATAAAGATG | 55833 |
rs758676941 | snp | C/T | 3.29772e-05 | 0.00406048 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953383 | AGACAAGGGCTTGGC[C/T]AAAGCCCTGCTGTTG | 55833 |
rs758714926 | snp | C/T | 0.000329435 | 0.01283 | missense | UBAP2 | GRCh38.p7 | 9:33941722 | TTATGCACAGAACTC[C/T]GGTCATAAGAGGAAG | 55833 |
rs758755147 | in-del | -/TGGGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037080 | GCAACCTCCGACTTC[-/TGGGA]TGGGATCAAGCGATT | 55833 |
rs758785786 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041590 | TAATCCCAGCTACTC[C/G]GGAGGCCGAGGCAGG | 55833 |
rs758798502 | snp | A/T | 1.65455e-05 | 0.00287619 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998779 | GATATCCTTTGCCAG[A/T]AACATACCTGCTTAA | 55833 |
rs758811516 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963813 | ACCAATGTAAAATTG[A/G]GGGTTTAAACATATG | 55833 |
rs758819408 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979567 | GCAACAAGAGAGAAA[C/T]TCCCGTCTCAAAAAA | 55833 |
rs758836291 | in-del | -/A | 1.6585e-05 | 0.00287962 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943593 | AGAAGCTGGGATCTG[-/A]AAAAGCAAAGCTGTC | 55833 |
rs758889702 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974530 | ACAAAAAAACACCAC[A/G]GTACCAACAGAGTAA | 55833 |
rs758891294 | in-del | -/G | 1.64849e-05 | 0.00287092 | frameshift-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927891 | GGTGTTCATGCTACT[-/G]GACAGGCTGGCGCCT | 55833 |
rs758909785 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042480 | AAGACTCCGTCTCAA[-/A]AAAAAAAAAAAAAAA | 55833 |
rs758910778 | snp | A/G | 1.70107e-05 | 0.00291634 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971805 | GAAGCAAACACCTAA[A/G]CCAAAATATTAACCA | 55833 |
rs758948600 | snp | A/G | 3.30846e-05 | 0.00406709 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998860 | CGCATCTGTTCAGCT[A/G]TTGCCTGGAAAGTAC | 55833 |
rs758988500 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991974 | CAAATGATACCCTGG[C/T]CAGGCACGGTGGCTC | 55833 |
rs758993155 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015345 | TTTTATTGAGACAGA[A/G]TCTCGCTCTGTTGCC | 55833 |
rs759008934 | snp | C/G | 1.64754e-05 | 0.00287009 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971714 | TTGTCCCACACACAT[C/G]TGTAGATGTAGAATC | 55833 |
rs759028028 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923954 | AGCTGGTGTGGTAGC[A/G]GGTGCAGGGGATGCA | 55833 |
rs759045238 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953765 | AACCTGGAGCAATAA[A/G]GTAAAATTAAACAAT | 55833 |
rs759055016 | snp | A/T | 1.64846e-05 | 0.0028709 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017128 | ACCTCGACAATGGTC[A/T]CTGCTCACTGAAGTC | 55833 |
rs759066634 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041426 | GCCAAGATCGCACCA[C/T]TGCACTCTAGCCTGG | 55833 |
rs759093915 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995330 | CTACTGCACTCCAGC[A/C]TGGGTGGCAGAGTGA | 55833 |
rs759132976 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009442 | AAAAAATATTTTTTA[G/T]GGAGACAGGGTCTCG | 55833 |
rs759134294 | snp | A/C | 1.64863e-05 | 0.00287104 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924167 | GGAGTTCGCGCTAGG[A/C]CGGCCCCGGGCTACT | 55833 |
rs759143396 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018357 | TTTAAAAACACAGAA[A/G]GCATCGGTGAGGATG | 55833 |
rs759168056 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994622 | GTCCCAGGTCAGTAA[A/G]CAAAAACTATTCAAA | 55833 |
rs759176825 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996662 | CAAATTTAATTCAAG[C/T]ACACAGGATTCCTAA | 55833 |
rs759190945 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964957 | CCATTTTAATAGGTG[A/T]ATGGGGGTAACTCAA | 55833 |
rs759204391 | snp | G/T | | | intron-variant, nc-transcript-variant | UBAP2, SNORD121A | GRCh38.p7 | 9:33952841 | ATTACCACATCATTG[G/T]TTTCTGGACTAAGAT | 55833 |
rs759213259 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33924213 | AAACTCACCTGGATA[C/T]GGATTATTAGCTAGG | 55833 |
rs759221280 | snp | C/T | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921371 | ATTGTAAAAGTCCAC[C/T]GAGATTTGGAAAAGA | 55833 |
rs759222408 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003752 | TGAGACAGAGTTTCA[C/T]TCTTGTTGCCCAGGC | 55833 |
rs759250419 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044926 | AAAACACCTACTCTA[A/C]TCCTTAATGTGAGCC | 55833 |
rs759261347 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036537 | CTGTCACAGGCAGCA[A/G]TACCCTGGAATCCTA | 55833 |
rs759272088 | in-del | -/TGGCT | 1.64875e-05 | 0.00287115 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924039 | CACTGCCCTTCCTCC[-/TGGCT]AACCAGAGAAAGGCC | 55833 |
rs759275759 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948211 | CAAATAAATGCAAGT[A/G]TTGTATAACAAAGGA | 55833 |
rs759294192 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989612 | AGGTAACAATCCTCT[C/T]GCTAAGCTCCTGTTG | 55833 |
rs759304928 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046746 | ATTTTATACTTAAGA[A/G]GGTAGATACCGGGAC | 55833 |
rs759314922 | snp | C/T | 0.000140895 | 0.00839211 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938848 | ATAGTTCACATGGTT[C/T]TTCTTGTTTCAGTGC | 55833 |
rs759318366 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955275 | CTGTAATCCCAGCAC[-/T]TTTAGGAGGCCGAGG | 55833 |
rs759335074 | snp | G/T | 1.64852e-05 | 0.00287094 | missense | UBAP2 | GRCh38.p7 | 9:33941665 | ATGATGGTTCCTGGA[G/T]CTGACTCTGATGAAC | 55833 |
rs759335174 | snp | C/G | 5.01224e-05 | 0.00500586 | missense | UBAP2 | GRCh38.p7 | 9:33927034 | TACGAGGTACTGGTT[C/G]TGCAGCAGGGGAGGC | 55833 |
rs759372661 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | UBAP2 | GRCh38.p7 | 9:33922977 | TCACCTGTGTCTTAT[C/T]GTAGACAGAACCAGT | 55833 |
rs759420360 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038232 | GAGGTGGGAAGATCA[C/T]GAGGTCAGGAGTTCA | 55833 |
rs759425015 | snp | A/G | 2.64855e-05 | 0.00363896 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927132 | CACCACAAAGAGTGA[A/G]AGTCCTCAGCTGCTT | 55833 |
rs759451790 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999903 | TGTATGTATGTATGT[-/T]ATGTTATTTTGAGAT | 55833 |
rs759462456 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955082 | CAGAGTAAAACTAGT[A/C]GAACTCAAATAAAAT | 55833 |
rs759475490 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983987 | TACAATCTCGGCTCA[C/T]TGCAGCCTCCACTTC | 55833 |
rs759503126 | in-del | -/CAGCAGTTGTTCCCAG | 0.000115442 | 0.00759656 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923060 | AGCAGTTGTTCCCCA[-/CAGCAGTTGTTCCCAG]CTCCAGGCTCCCCAC | 55833 |
rs759503451 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972138 | AGTCAGAATCCAAGT[C/T]TGGCTTTTACAGCTT | 55833 |
rs759504923 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010430 | AACTCTGCCTCATAA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs759550194 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978631 | TAAAAATACAAAAAA[C/T]TAGCCCGATGTGCTG | 55833 |
rs759555018 | snp | A/G | 8.27e-05 | 0.00642986 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927934 | CTTGAGACGGAGGTC[A/G]CTGCCGTGGAGAAGG | 55833 |
rs759556753 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959691 | TGCTCAAAAATATCT[A/G]TGCAATAAAGGAATT | 55833 |
rs759571602 | snp | C/T | 1.64833e-05 | 0.00287078 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996324 | GATTTTTCCCTGTCA[C/T]TTCCATAAGCTAGTG | 55833 |
rs759603469 | snp | C/G | 1.64795e-05 | 0.00287045 | missense | UBAP2 | GRCh38.p7 | 9:33960858 | CTGTTGTCCACTCTT[C/G]CACAGAATTCTTCCA | 55833 |
rs759610789 | snp | C/T | 1.78704e-05 | 0.00298913 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922644 | AGGCTGGAGCAGAAC[C/T]CCTGGCCCAGAGTAG | 55833 |
rs759615177 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048068 | TGCGTGGGCAACTAA[C/T]TAGACTAAAAACTCA | 55833 |
rs759620066 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041300 | TCTACTAAAAATGCA[-/A]AAAAAAAAAAAAAAA | 55833 |
rs759621967 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33944429 | TGTGGCTGGTGGACA[A/G]ACACAGAGATATTTT | 55833 |
rs759622156 | snp | A/G | 1.66371e-05 | 0.00288414 | missense | UBAP2 | GRCh38.p7 | 9:33963731 | GTATTCATACCTTTG[A/G]GTCCATAAGAACTTT | 55833 |
rs759655067 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934640 | CCTTGTATTATGATG[C/G]TAACAGCTTCACAGG | 55833 |
rs759670238 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024208 | TTAGCCGGGCGTGGG[A/G]GCACATGCCCATAAT | 55833 |
rs759699957 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955512 | GCGACAGAGTGAGAC[G/T]CCGTCTCAAAAAAAC | 55833 |
rs759702992 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978555 | AGGCAGGCGGATCAC[A/G]AGATCAGGAGATCAG | 55833 |
rs759705032 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991110 | GCCAACATTGTGAAA[C/T]TCTTATCTCTACTAA | 55833 |
rs759721043 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933670 | AGCAGATCTGTTTAT[C/T]TCTAAAACCAATCCT | 55833 |
rs759721895 | snp | A/C | 1.74888e-05 | 0.00295704 | missense | UBAP2 | GRCh38.p7 | 9:33922583 | GAGCTGGGCTGGCTG[A/C]GCTGACCCGAGCCAC | 55833 |
rs759728568 | snp | C/G | 8.27739e-05 | 0.00643274 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933526 | CTGCTAGTCAGGTCG[C/G]CAGTGTGCTGGGATG | 55833 |
rs759745070 | snp | G/T | 1.64751e-05 | 0.00287007 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986739 | ATTGAAAGCATTTTC[G/T]TCCCTCTTACTCTAG | 55833 |
rs759792627 | in-del | -/TATGTATGTATGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999895 | ATGTATGTATGTATG[-/TATGTATGTATGT]TATTTTGAGATGGAG | 55833 |
rs759796278 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974341 | GCAAAACCTTGTCTC[C/T]ACAAAAAATACAAAT | 55833 |
rs759810490 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015032 | ATCTCCTCACTATGT[-/C]CCCTAACATCAACAG | 55833 |
rs759814876 | snp | A/G/T | 3.304e-05 | 0.00406437 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924319 | CTTGATCAGCGACTG[A/G/T]CCCTGCTTGACTCCC | 55833 |
rs759820022 | in-del | -/GC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950416 | AAAAACAAATACTTT[-/GC]GCCTTCCCTCAAGTA | 55833 |
rs759838241 | snp | A/C | 1.64795e-05 | 0.00287045 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986812 | GTCCACTTGATTGCA[A/C]TCAATTCCATTTTCT | 55833 |
rs759847052 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949469 | GCACTTTGGGAAGCC[A/G]AGGTGGGTGGATCAC | 55833 |
rs759870166 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010636 | ATTGACTGTACAACT[C/G]TCAACTTTTCTTCAT | 55833 |
rs759883952 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011910 | TTCAAATGAATCCAA[A/G]TTTTTTTTAATTAGA | 55833 |
rs759911631 | snp | C/T | 1.64743e-05 | 0.00287 | missense | UBAP2 | GRCh38.p7 | 9:33923197 | CTACCTTTGCCAGGC[C/T]CAGAACCTGCAGACT | 55833 |
rs759949996 | in-del | -/ACAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945495 | CAGACTGGGTGACAA[-/ACAA]ACAAACAAACAAAAA | 55833 |
rs759963704 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030700 | GGGAGGCCCGGGCGC[A/G]TGGATCACAAGGTCA | 55833 |
rs759965147 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020239 | AATACTACCGTCTTC[C/T]ATCTCCACATCTGTC | 55833 |
rs759975643 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953366 | GTGTTGCGAATTTGT[A/G]AAGACAAGGGCTTGG | 55833 |
rs759978365 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944043 | TCTATTTTTGGGGAC[C/T]CACCAATGATGAAAG | 55833 |
rs759980460 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956597 | ACCTCCCAAAGTGTT[A/G]GGATTACAAGTATAA | 55833 |
rs759989236 | in-del | -/CCC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965263 | CTTCTTCCATTTTTT[-/CCC]CCCATTTTTAATTGC | 55833 |
rs759996368 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930531 | TGTGGGGATACACAA[C/G]TGGGGAAAAAAAAGT | 55833 |
rs759997508 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923305 | TAACCTAGCGTGGCA[A/G]GGTACAAGAGGCAAG | 55833 |
rs760022245 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34048965 | GGGCGAAGGAGGAGC[C/T]ACAACACGTCGCTCG | 55833 |
rs760023919 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030914 | CAACCTGGGCGACAG[A/G]GCAAGACTCATCTCA | 55833 |
rs760029194 | in-del | -/TAAA | 1.87912e-05 | 0.00306516 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941903 | ATAATTTTGTTACTT[-/TAAA]TAGCTTCATAAAAAA | 55833 |
rs760058361 | snp | C/T | 3.30426e-05 | 0.0040645 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998847 | CACTTGAGCGAGACG[C/T]ATCTGTTCAGCTGTT | 55833 |
rs760066096 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998987 | ACAACAAATAAAAGA[C/G]AGTGAATTTAGGCCT | 55833 |
rs760091202 | snp | A/G | 3.34314e-05 | 0.00408835 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943403 | TTTGCTTCATAACAA[A/G]GGACTAAATTCAGTA | 55833 |
rs760102232 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948033 | TCCACATTCTATGTT[C/T]TATCACCACCCTCTT | 55833 |
rs760128106 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936767 | GTAAATTAACAACTT[A/G]GATGAAATGGACAAA | 55833 |
rs760129073 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | UBAP2 | GRCh38.p7 | 9:33941830 | GAGTTCTGTACTGCA[C/G]TGGTCATTGATAAAG | 55833 |
rs760227452 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994130 | CAAACTCCTGACCTC[A/G]TGATCTGCCCACCTA | 55833 |
rs760281900 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981220 | GATATATATATATAT[A/T]TTCTGGATATATATA | 55833 |
rs760289900 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33971706 | TACTAGCTTTGTCCC[A/G]CACACATCTGTAGAT | 55833 |
rs760307532 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007069 | AGTTCTAACAGATGT[C/T]TGATGGAGTTTTTAG | 55833 |
rs760332858 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963947 | CTTACAGGTCACTGC[A/C]AATCAAGTTATGAAT | 55833 |
rs760345805 | snp | A/G | 0.000205656 | 0.0101383 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017016 | ATAAAAGAAAAAAAA[A/G]GAAAAAAAAAAAAAG | 55833 |
rs760358336 | snp | A/C | 6.60022e-05 | 0.00574428 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924017 | TAGGAAAGAGCACTG[A/C]CTCCAGCCACTGCCC | 55833 |
rs760396339 | snp | A/G | 3.30453e-05 | 0.00406467 | missense | UBAP2 | GRCh38.p7 | 9:33948407 | AGGACTGGGATGTTG[A/G]GGGCTTGAGGTCCCA | 55833 |
rs760418014 | snp | C/T | 0.000378978 | 0.0137603 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935792 | TATCCTCTTCCTCTG[C/T]TTGGTTGGCACCAGC | 55833 |
rs760426063 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959655 | CTTATAGACTGACAG[C/T]ACCCAGAAGCTAGTG | 55833 |
rs760438273 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937468 | AAAAATTAGCTAGGT[A/G]GGGTGACACACACCT | 55833 |
rs760448754 | snp | C/T | 3.53651e-05 | 0.00420491 | missense | UBAP2 | GRCh38.p7 | 9:33922862 | GTCCCTGCATGAAAT[C/T]CCTGCTTGTCAAAAG | 55833 |
rs760466147 | snp | A/C | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050718 | ATACAAAAAAATGTC[A/C]GGGCGCGGTGGCTCA | 55833 |
rs760466629 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993131 | TTCCTTTGTGACAGA[C/T]ATACTTACATAAGAA | 55833 |
rs760490429 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001418 | AAGCTTTTGGGAGCT[A/G]GTAAGCTCTGATTGG | 55833 |
rs760509013 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926881 | GGTGCTCAGGGATGG[A/G]AGGGCAGCTCAAGGT | 55833 |
rs760519783 | snp | C/G/T | 4.94485e-05 | 0.00497214 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924163 | TCCTGGAGTTCGCGC[C/G/T]AGGCCGGCCCCGGGC | 55833 |
rs760538718 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956623 | TATAAGCCATGGCGC[C/T]CGGCTGCAAGTGAAG | 55833 |
rs760560337 | in-del | -/A | 1.6477e-05 | 0.00287024 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33922995 | GACAGAACCAGTCAT[-/A]ATCAGGTAGACCAGT | 55833 |
rs760565642 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009504 | AGCTCAAACAATCCT[A/C]CCACCTCAGCCTCCC | 55833 |
rs760582453 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958700 | GCATGAGCCACTGTG[C/T]CCGGCCTTTTTTTTT | 55833 |
rs760651468 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015278 | AATAATATAACCAAA[C/T]TGAGGAGGAGGGAGT | 55833 |
rs760664542 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970909 | CTGGGTTCAAGCGAT[C/T]CTCCTGTCTCAGCCT | 55833 |
rs760689623 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983175 | GAGCCACGGTGCCCG[G/T]CCCCCCTATAATGTG | 55833 |
rs760701052 | snp | A/G | 1.64814e-05 | 0.00287061 | stop-gained, missense | UBAP2 | GRCh38.p7 | 9:33960848 | GTCCAGTCTTCTGTT[A/G]TCCACTCTTCCACAG | 55833 |
rs760729739 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967424 | TTCAATATATCACCA[C/T]TGACTGTAACACCTG | 55833 |
rs760751355 | snp | C/T | 1.65787e-05 | 0.00287907 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956175 | TGAAAAATTTAATCT[C/T]ATTCTACATACTACT | 55833 |
rs760754568 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988711 | TGATACGAAACCACA[C/T]GGGAGGCGCTTATGA | 55833 |
rs760756573 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026371 | AACAGAAAAACTAAT[-/G]GTTTTTTTCAAACCA | 55833 |
rs760761826 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933400 | CGTCAGAGACAACAA[G/T]TGTGCTCTGTTCATG | 55833 |
rs760765266 | snp | A/T | 3.29554e-05 | 0.00405914 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989060 | TTTTCTTCTCTCTAT[A/T]CTCTTTGTTTTCTGA | 55833 |
rs760772544 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923804 | ACTCACAAACATGGT[A/G]GGGCCATACTGGAAG | 55833 |
rs760783245 | snp | C/T | 1.66438e-05 | 0.00288472 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996190 | GGAATTGGAGACAAA[C/T]GTAAACAATGCAAAT | 55833 |
rs760806314 | snp | A/C | 1.66668e-05 | 0.00288672 | missense | UBAP2 | GRCh38.p7 | 9:33927028 | GGGACCTACGAGGTA[A/C]TGGTTGTGCAGCAGG | 55833 |
rs760806588 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948091 | TGCATTTACACAAAG[C/T]GTTAGATGTTCATAT | 55833 |
rs760813677 | snp | C/T | 1.6819e-05 | 0.00289987 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017177 | AAAATAATGTATGTA[C/T]AAAATAGAAAATCTG | 55833 |
rs760824329 | in-del | -/A | 3.40391e-05 | 0.00412533 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941625 | CGGACATCTTCTGAG[-/A]AAAAAAACTAAAATA | 55833 |
rs760838076 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040326 | GAGACTCTGTCTCAA[-/AAAA]AAAAAAAAAAAAAAA | 55833 |
rs760841424 | snp | C/T | 1.68755e-05 | 0.00290473 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943635 | AGAGGTCACAGATTC[C/T]AGGTCACAAAGGCCT | 55833 |
rs760854843 | snp | A/C | 1.64822e-05 | 0.00287068 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923505 | AGCAGATGAGGTATT[A/C]GTGTAGGAAGAGGCA | 55833 |
rs760906799 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989350 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAAC | 55833 |
rs760928752 | in-del | -/CCA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955477 | TGAGCCGAGATCGTG[-/CCA]CCACTGCACTCCAGC | 55833 |
rs760943172 | snp | A/C | 2.41712e-05 | 0.00347635 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922488 | CCTTGCCCCAGCCCA[A/C]CCCTCTCTTCTGGGT | 55833 |
rs760961521 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034903 | AAAAAAAAAACGAAT[C/T]GCTCAACTGTTCTCT | 55833 |
rs760961762 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964921 | CTCACCAGCACTTGG[A/C]ATTTTTCATTTCCTT | 55833 |
rs760980299 | in-del | -/GT | 0.000127978 | 0.00799829 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927107 | GAAAAATCAAATGGA[-/GT]GAAATGGTCACCACA | 55833 |
rs760984681 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047923 | CTTCCTTGAATGTGA[A/G]GTAAAAACAATATCC | 55833 |
rs761001015 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984313 | AGGGACTAATATTCA[A/G]ACAATACAAGGAATC | 55833 |
rs761015237 | snp | C/T | 1.76983e-05 | 0.0029747 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932650 | GACAAAACAGAGCGC[C/T]GTATGTCCACCTGAA | 55833 |
rs761018405 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011789 | CAAGTTGAAAAATAT[A/C]TTGCCAAGAAAAGTA | 55833 |
rs761028349 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989548 | AGCTTGCAGCTCACC[G/T]GCTTATCATTTAAAT | 55833 |
rs761043274 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978838 | AGTCACTAAATACAA[A/T]ACAGTAAGGTAAAGC | 55833 |
rs761100974 | snp | C/G/T | 8.6562e-05 | 0.00657833 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922564 | TTGAGACTTGGGCTG[C/G/T]AGGGAGCTGGGCTGG | 55833 |
rs761115371 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955247 | AAGTTTAGGCCAGGC[A/G]CGGTGGCTCACACCT | 55833 |
rs761189029 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950997 | TGGGAAATATCATCA[C/T]CACTTCTGTTGCTGC | 55833 |
rs761200550 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | UBAP2 | GRCh38.p7 | 9:33923189 | GGTAAACACTACCTT[C/T]GCCAGGCCCAGAACC | 55833 |
rs761200901 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033077 | TCTGGAAAAAACTAA[A/C]AATTGAGCTACCATA | 55833 |
rs761216676 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930382 | ATTCTCTGTGGTATC[A/G]AGACTGAAAACGACC | 55833 |
rs761216729 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962147 | AAAGGAAAATTTCCA[A/G]GAGAAAAACAATGAT | 55833 |
rs761218150 | snp | C/G | 4.94401e-05 | 0.00497168 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986721 | GCCTGCTTCTTCCCC[C/G]TAATTGAAAGCATTT | 55833 |
rs761219914 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033740 | GCATCAAATCAATTC[-/T]TTTTTTTTTTTTTTA | 55833 |
rs761226861 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033418 | TAAAAATCAAAACAA[C/T]TGAACTCATAATCAC | 55833 |
rs761247294 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040943 | TAGCATTACTTAGTA[A/G]AAGTTACACATACCC | 55833 |
rs761276757 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954031 | CGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55833 |
rs761325713 | snp | G/T | 5.64562e-05 | 0.00531271 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953243 | TACATTTGCTAATGG[G/T]TATATTTCTTAAAAT | 55833 |
rs761333556 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001567 | ATCCCTGGGCAAGCG[A/G]TTTGTGCCCCAAGCA | 55833 |
rs761339940 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947983 | GAAGACCCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs761341970 | snp | C/T | 4.94849e-05 | 0.00497393 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953357 | CTGATTGTTGTGTTG[C/T]GAATTTGTGAAGACA | 55833 |
rs761346182 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | UBAP2 | GRCh38.p7 | 9:33941702 | GGCTTTGGTATGGGA[C/T]CCTGTTATGCACAGA | 55833 |
rs761363955 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031968 | ATAGCAAGACCTCCT[A/C]ATCTCTACTAAAAAA | 55833 |
rs761409266 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985331 | GCATTTATCATTTCT[A/T]TGTGTTGGGAACTTT | 55833 |
rs761435802 | snp | A/G | 1.66638e-05 | 0.00288645 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996385 | AAAAACTGGCACTTG[A/G]TATTAAGATTCTTCT | 55833 |
rs761457417 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978326 | ATCACTTGAGCCACA[A/G]TAGTTTGAGATCACC | 55833 |
rs761507084 | snp | C/T | 1.65373e-05 | 0.00287548 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927933 | ACTTGAGACGGAGGT[C/T]GCTGCCGTGGAGAAG | 55833 |
rs761523608 | snp | C/T | 8.23798e-05 | 0.00641741 | missense | UBAP2 | GRCh38.p7 | 9:33923998 | CAAACTTTGTGACAT[C/T]ACCTAGGAAAGAGCA | 55833 |
rs761542340 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969554 | ATGCTCTCTCTTTAA[-/A]AAAAAAAAAAGAAAG | 55833 |
rs761542762 | snp | C/T | 1.65211e-05 | 0.00287407 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971624 | CAAACATTTAAAACT[C/T]ATCTCTGGCAAAAAC | 55833 |
rs761575885 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927873 | CAGACAGAGGCTGTT[C/T]GCGGTGTTCATGCTA | 55833 |
rs761605662 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003965 | CCTCAGGTGATCCGC[C/T]CACCTCGGCCTCCCA | 55833 |
rs761608111 | snp | C/T | 5.425e-05 | 0.00520789 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922669 | GAGTAGGGTGGCTGC[C/T]TCCATCACTGTACTC | 55833 |
rs761627684 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959434 | TGTATATAGTTTTGA[A/G]GATCTGTATTTGTAA | 55833 |
rs761630968 | snp | C/G | 1.65345e-05 | 0.00287524 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971758 | GGATTAAATGTCCTG[C/G]GGTTTGAAATAAAGA | 55833 |
rs761644280 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001966 | TTATATTTTTTCATT[-/A]AAAAAAAAAAACAAA | 55833 |
rs761651751 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019899 | GTCGCGGTGGCTCAT[-/A]ATCTGTAATCCTAAC | 55833 |
rs761661680 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923921 | GTGGTGGGTCTGTGA[C/T]TGGCTCTGCTGTGGC | 55833 |
rs761697462 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936560 | CAGCCTCCCAAAATG[G/T]TGGGATTACAGGTGT | 55833 |
rs761712343 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985597 | ACACGTACTCACTCA[C/T]GTGGGAGCTAAAAAG | 55833 |
rs761716033 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938898 | CTCTAACTTATTTCT[C/G]TCAAAGCATCTCTGA | 55833 |
rs761735872 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946875 | TGCAGAAAAAGTTAA[C/T]ATAGGGACCTACAAT | 55833 |
rs761776030 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026697 | GTACAGTATTAAGTC[A/C]CTAATCTTTCCAACA | 55833 |
rs761787512 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993036 | TACATTAATTCAAGA[A/G]ACCGATACTTCAAAA | 55833 |
rs761792859 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042550 | CCCAGGACTCTGGGA[A/G]GCCAAGCAGGAGGAT | 55833 |
rs761831750 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950826 | CCTAGGTAATACACA[A/G]CATAGGCCTCTTAAG | 55833 |
rs761862167 | snp | A/C | 1.66701e-05 | 0.002887 | missense | UBAP2 | GRCh38.p7 | 9:33948389 | CAAGATGACTGAGGA[A/C]TGAGGACTGGGATGT | 55833 |
rs761875930 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028888 | GACTGGGGTAATTAG[A/G]AACTGGGCCGCACAG | 55833 |
rs761889761 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934935 | CTGGGGCTCCAAATC[C/T]GTCATTACAGTTTCA | 55833 |
rs761902796 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946578 | ACAACCTAATATTTT[A/C]GCCTTTGTGTCTCAT | 55833 |
rs761912159 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993802 | CTATTTTCTTATCTT[C/T]GAAGAAAACAAGAAG | 55833 |
rs761923471 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988702 | GGTCAATGCTGATAC[A/G]AAACCACATGGGAGG | 55833 |
rs761929330 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006473 | TTGCTCGAGCTCAGG[C/T]GTTTGAGACCAGCCT | 55833 |
rs761955919 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015006 | ACTGAAAAATGTAAC[A/G]CAACACTTAAATCTC | 55833 |
rs761980689 | snp | A/G | 1.68131e-05 | 0.00289935 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953493 | AGCAGACAAAAAGCA[A/G]TGAGGAACCAGTCAT | 55833 |
rs761988066 | snp | A/T | 6.81269e-05 | 0.00583599 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926944 | AGGTGCCAGCCCCCG[A/T]GGCCAGGGGAGCTGG | 55833 |
rs762001708 | snp | A/C/T | 6.60582e-05 | 0.00574677 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956159 | AAGCTGTATGGAAAG[A/C/T]TGAAAAATTTAATCT | 55833 |
rs762005899 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977048 | TTTTATTTATTTTTT[-/A]TTTTTTTTGAGACAG | 55833 |
rs762037235 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957746 | ACTCAAAATGTTCCC[A/G]TAATTCTTATCAACT | 55833 |
rs762077817 | snp | A/C | 1.66493e-05 | 0.0028852 | missense | UBAP2 | GRCh38.p7 | 9:33927018 | GCAGTCCTCCGGGAC[A/C]TACGAGGTACTGGTT | 55833 |
rs762081697 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040159 | GCTAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs762103211 | snp | A/C | 1.67466e-05 | 0.00289362 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943622 | TCGTGTCAGGAACAG[A/C]GGTCACAGATTCCAG | 55833 |
rs762110071 | snp | G/T | | | utr-variant-5-prime, intron-variant | UBAP2 | GRCh38.p7 | 9:34048828 | GATGGCAATTACCGC[G/T]GCTGCTCTCGGAGGA | 55833 |
rs762116755 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050584 | ATTAAAGAATGCTGC[C/T]GGGCGTGGTGGCTCA | 55833 |
rs762120729 | in-del | -/AAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026885 | GTTCAGTCACAGATA[-/AAT]AATAGTTCCCAATTC | 55833 |
rs762137662 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033280 | GAGTACTACTTAGCC[A/G]TAAAAAAGAATGAGA | 55833 |
rs762151912 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001356 | GAGTTTTATTAGAAA[A/G]AGAAATGTGACCTAT | 55833 |
rs762191054 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33944396 | ATCCGCCGCTTAGCA[A/G]GTTTGATGTGTTTGG | 55833 |
rs762193093 | snp | C/T | 3.31807e-05 | 0.00407299 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932549 | AGGAAGAGGAAGCCG[C/T]GCAGACACTTACTGT | 55833 |
rs762232450 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018079 | TGCAATCCCAGCTAT[A/T]TTGAGGCTAAGATGG | 55833 |
rs762235089 | snp | A/G | 4.94295e-05 | 0.00497115 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923486 | GGAGGGACCTGGGGG[A/G]GCAAGCAGATGAGGT | 55833 |
rs762238971 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010564 | AGATAAAATAATGGC[-/T]TGGCTAAACAGATGT | 55833 |
rs762246038 | snp | A/G | 0.000280549 | 0.0118404 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922531 | GTATGGAGAGTTGCC[A/G]TAGGCAGGTTTGGAG | 55833 |
rs762255784 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966778 | AGTAAAGAAGTACCA[C/T]AATTATATTTTAATG | 55833 |
rs762280479 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953995 | CACTGCAACCTCTGC[C/T]TCCCAGGCTTAAGCG | 55833 |
rs762292774 | snp | C/T | 3.9921e-05 | 0.00446754 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922469 | CTCTCCTGCCCAGGA[C/T]AAGCCTTGCCCCAGC | 55833 |
rs762309235 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926138 | CCCAGAAGAGACCTT[-/A]AAAGACCATCAGCTC | 55833 |
rs762309818 | in-del | -/AC | 3.31419e-05 | 0.00407061 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998877 | GCCTGGAAAGTACAT[-/AC]ACAATTGTTAAGGAT | 55833 |
rs762327396 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991810 | AATTCCAGAGGTCCT[A/G]GAAAAATCATCCCAG | 55833 |
rs762336400 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930105 | AAGGATGTACAACCT[C/T]ATTAAAAACTAGACT | 55833 |
rs762361425 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33924236 | TAGCTAGGCTCCCAT[C/T]TCGGCTGGCAAGCGC | 55833 |
rs762402453 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002910 | CCAGATTAATATTGA[A/G]CCCCCCGAGCTTAAG | 55833 |
rs762407169 | snp | C/T | 0.000116539 | 0.00763257 | missense | UBAP2 | GRCh38.p7 | 9:33927021 | GTCCTCCGGGACCTA[C/T]GAGGTACTGGTTGTG | 55833 |
rs762419145 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978253 | GAAATTTAAACGTAA[A/G]CTGGGTCTGGTGGCT | 55833 |
rs762434546 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038065 | TCCCAGGTACCCAAG[A/T]GGCTAAGGTGGATCA | 55833 |
rs762458760 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956298 | AGTGACCATGACAAG[C/T]AATTTTCAAGTGAAT | 55833 |
rs762461213 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929304 | CTTGCTGAAAGGGAC[A/T]CAAGAGTCATCTGGC | 55833 |
rs762464354 | snp | A/T | 1.64845e-05 | 0.00287089 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973241 | CACGTCCAAATCCTT[A/T]AAAAAAACACACAAT | 55833 |
rs762466017 | in-del | AGGAGGAGGAGGAAGAGGAGGAAGAGAAGGAGGAAGAGGAGGA/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016247 | AGGAAGGGGAGGAAG[lengthTooLong]GGAGGAAGAGGAGGA | 55833 |
rs762535268 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954708 | GACAATGATCCCAGT[-/A]AATTCACTGAATCAT | 55833 |
rs762567585 | in-del | -/GGGGAGGAGGAGGAGGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939857 | GGGGAGGAGGGGGAG[-/GGGGAGGAGGAGGAGGA]GGGGAGGAGGAGGAG | 55833 |
rs762574901 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018259 | TTTAGACAGAAGAGC[C/T]GGGAATTTTCCGATA | 55833 |
rs762584274 | snp | C/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018547 | GCAGAGTCTCAAAGA[C/G/T]ATGCTTGTACTTCCA | 55833 |
rs762586470 | snp | A/G | 1.67713e-05 | 0.00289575 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948636 | CAATACAGAATTTCT[A/G]CCCAAGGCTTTAAAA | 55833 |
rs762622173 | snp | A/G | 0.000131824 | 0.00811755 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923174 | ATCCTGGAAAGGAGA[A/G]GTAAACACTACCTTT | 55833 |
rs762624672 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992971 | ACTCTCCCACCACTT[C/T]GCCTTTGCCAAAAAC | 55833 |
rs762639104 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | UBAP2 | GRCh38.p7 | 9:33941782 | GATGAGCTTGTCAGA[C/T]TGCAGGAGGTAATGA | 55833 |
rs762643280 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973320 | ATCCTATACTCACTA[-/C]CCCAGACAATATTAT | 55833 |
rs762683706 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025711 | AATAGTTTTGGAAAA[A/C]AGTTTTAACTGCCTA | 55833 |
rs762683886 | snp | C/T | 1.64936e-05 | 0.00287168 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963759 | TTTTGTTTGACAGAT[C/T]CTGAGCTATGTTGTG | 55833 |
rs762694486 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029641 | AGGAGTTCGAGACCA[C/G]CCTGGGCAGCATAGC | 55833 |
rs762701942 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941676 | TGGAGCTGACTCTGA[C/T]GAACTCACAGGGCTT | 55833 |
rs762713927 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941231 | TTTATCTATAGTCCA[C/G]TATTATTAACAAAAA | 55833 |
rs762719785 | snp | G/T | 1.80244e-05 | 0.00300197 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927770 | AGGGGCTCAGGGGTG[G/T]GCAGGAAAGGCCTCT | 55833 |
rs762730166 | snp | C/T | 1.65198e-05 | 0.00287395 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996216 | CAAATCAATTAATAA[C/T]ACTTACTGTGTCTGA | 55833 |
rs762739910 | snp | G/T | 3.29473e-05 | 0.00405864 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923831 | GAAGGCACTGGGCAT[G/T]CCTGTGTAGTAGGGA | 55833 |
rs762743717 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017150 | ACTGAAGTCATCATA[A/T]ACAGTATATACAAAA | 55833 |
rs762761618 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960976 | TGCGGGGAAAAAAGA[C/T]ACATACGCCTCACTA | 55833 |
rs762769488 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022433 | ACACAGCAAGACCCC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs762823526 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948293 | TGGACAAATTCCACA[C/T]TAGTCTTCACAAGTC | 55833 |
rs762827393 | in-del | -/AGAAG | 1.64817e-05 | 0.00287064 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935890 | CATTCTATAAGGAAA[-/AGAAG]AGAAGAGAATATAAA | 55833 |
rs762854759 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938885 | TCAGGATATAGACTC[-/T]TAACTTATTTCTGTC | 55833 |
rs762855948 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005111 | ACACTAAAAATACAA[A/C]AATTAGCAGTGCGTG | 55833 |
rs762862673 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934815 | CCTGCCACTACCACT[A/G]CTAGAGTCAAAAGTT | 55833 |
rs762956487 | snp | G/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050401 | ATCATTTTCACACTC[G/T]ACCCATCGGGCCCAA | 55833 |
rs762964094 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962079 | AGTTAATGAAAGCCA[G/T]AATTGTAAGAGAAAG | 55833 |
rs762992792 | snp | C/T | 3.31466e-05 | 0.0040709 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971604 | ACATACAACTCTTAA[C/T]AGCTCAAACATTTAA | 55833 |
rs763010532 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970627 | TTAGTATAGATGAGG[C/T]CTTACTATGTTAACC | 55833 |
rs763013075 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991307 | CTCTGTATCAAAAAT[A/G]ATAATAATAATAACG | 55833 |
rs763019991 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012981 | CCAACATGGTGAAAC[C/T]CCTCTCTACTAAAAC | 55833 |
rs763030034 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | UBAP2 | GRCh38.p7 | 9:33944504 | GGACTGTCTCCAGGT[A/G]TTGATTCTCGAAGTT | 55833 |
rs763040322 | snp | C/G/T | 4.94975e-05 | 0.0049746 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33926641 | CCGTGACTGCAGCAT[C/G/T]TGGAGCTCGTCATAG | 55833 |
rs763075750 | snp | C/T | 1.80991e-05 | 0.00300819 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922744 | GGGCTGCTGGTGGGC[C/T]GGCAAGATGTGTAGG | 55833 |
rs763115762 | snp | A/G | 1.65091e-05 | 0.00287303 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933547 | TGCTGGGATGTGGAC[A/G]GCAGAAGTGCAGTGC | 55833 |
rs763120805 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944104 | CAACTATGGGATACA[A/G]CAAAACCCTCAAGAA | 55833 |
rs763170284 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969710 | TGCCACTAAAAATAC[G/T]AAAAAGTTAGCCAGG | 55833 |
rs763172027 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026547 | GTCTATCTCAAACTG[G/T]CAAGGATGGGTCTCA | 55833 |
rs763194222 | in-del | -/AAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030450 | CAGATTCCATCTCAA[-/AAAC]AAACAAACAAACAAA | 55833 |
rs763198000 | snp | A/C | 1.64738e-05 | 0.00286995 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923319 | AGGGTACAAGAGGCA[A/C]GTGTGAGCCAGGCAA | 55833 |
rs763223890 | in-del | -/AG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047976 | TGGATTACATCAAAC[-/AG]GAAATAACAGTAATA | 55833 |
rs763247948 | in-del | -/TTTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994463 | TATTCCCAAAGATTT[-/TTTC]TTTTTTTTTTTTTTC | 55833 |
rs763271258 | in-del | -/C | 6.66278e-05 | 0.00577143 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996186 | CTACGGAATTGGAGA[-/C]AAATGTAAACAATGC | 55833 |
rs763296853 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013855 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGGCTC | 55833 |
rs763305160 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936286 | CACACCCAGACCCAA[A/G]TAATTTTTTTTTAAA | 55833 |
rs763328171 | snp | C/G | 1.64789e-05 | 0.0028704 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33956132 | TGAGGCAGTGAAGAC[C/G]TTTGTTTCAGAAAGC | 55833 |
rs763355601 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976943 | CTTGAACCTGGGAGG[C/T]AGCAGTCGCAGTGAG | 55833 |
rs763358985 | in-del | -/AAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011587 | CAATAAATATTTGAT[-/AAAC]AAAGCACCAAACATA | 55833 |
rs763372358 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975996 | CAAGGCAGGAGGATC[A/G]CTTGAGGCCAGGAGT | 55833 |
rs763386572 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995315 | TGAGTCAAGATCACA[A/C]TACTGCACTCCAGCC | 55833 |
rs763388136 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932363 | TTCTTCCCAGGCGCT[A/G]CAAACTTAGAAAGCA | 55833 |
rs763408716 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943440 | AGACTTCGAATACAA[A/G]CTGATGGGAATCTGA | 55833 |
rs763417100 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944897 | GTGAGAACAATATTA[C/T]GGTGCTATACACACC | 55833 |
rs763480661 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935164 | GCTGTTGGAAGTGGC[-/GGG]GGGGGGGGGTCTCAT | 55833 |
rs763504283 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987079 | GGCAGATCTCTTGAG[C/T]CCAAGAGCTTGAGAC | 55833 |
rs763548359 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929308 | CTGAAAGGGACTCAA[A/G]AGTCATCTGGCAAGT | 55833 |
rs763588609 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | UBAP2 | GRCh38.p7 | 9:33922997 | ACAGAACCAGTCATA[C/T]CAGGTAGACCAGTGG | 55833 |
rs763618253 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant, splice-donor-variant | UBAP2 | GRCh38.p7 | 9:34017049 | TTCCACAAAAACTTA[C/T]CTGTACCACTTGTTT | 55833 |
rs763640785 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941280 | ATTTTAACACAAAAA[G/T]ACCTAACAGTGATGA | 55833 |
rs763643242 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972398 | CTTAAAGTGCTCCTG[A/G]GAGTTTGCTCCCTGT | 55833 |
rs763645241 | snp | C/G | 1.64762e-05 | 0.00287016 | missense | UBAP2 | GRCh38.p7 | 9:33941699 | CAGGGCTTTGGTATG[C/G]GATCCTGTTATGCAC | 55833 |
rs763650482 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002966 | GCGCTAGGATTACAG[A/G]CATAAACCACAGTGC | 55833 |
rs763664200 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989853 | GGAATACAACCTTGC[C/T]TGTTCCATTATTCAA | 55833 |
rs763665342 | snp | A/G | 1.7957e-05 | 0.00299636 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927774 | GCTCAGGGGTGGGCA[A/G]GAAAGGCCTCTGGAG | 55833 |
rs763668828 | snp | A/G | 1.65064e-05 | 0.00287279 | splice-donor-variant | UBAP2 | GRCh38.p7 | 9:33996221 | CAATTAATAATACTT[A/G]CTGTGTCTGAATTCC | 55833 |
rs763686232 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961039 | TTCTTAATCTATTCT[C/T]GGTAAAATCAGTAAT | 55833 |
rs763704941 | snp | C/T | 0.000214938 | 0.0103645 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938932 | GGTAATTTTAATCTG[C/T]GGATATTCCAGGCTG | 55833 |
rs763739891 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928404 | AGTCTGAGAAGAGGC[A/G]AGCACAGGCCACAGG | 55833 |
rs763742453 | snp | A/G | 1.88677e-05 | 0.0030714 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953239 | AGAATACATTTGCTA[A/G]TGGGTATATTTCTTA | 55833 |
rs763755389 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020737 | TGATCTCTGCTCACC[A/G]CAAGCTCTGCTTCCT | 55833 |
rs763756617 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996371 | GTTAGAGGCAAACAA[A/G]AAACTGGCACTTGAT | 55833 |
rs763763242 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003961 | CTGACCTCAGGTGAT[C/T]CGCCCACCTCGGCCT | 55833 |
rs763787959 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958772 | GTAATCTCAACTACT[A/T]GGAGGCTGAGGCAAG | 55833 |
rs763791712 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947827 | AAGATCCTGACTCAA[-/A]AAAAAAAAAAATAAA | 55833 |
rs763809318 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017152 | TGAAGTCATCATATA[C/T]AGTATATACAAAATA | 55833 |
rs763809429 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995923 | CATAAGCAACAGAGC[C/G]AAGAGATGCTTTTCA | 55833 |
rs763873431 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999211 | AATCTTGGCGGGGCA[C/T]GGTGGCTCATGCCTT | 55833 |
rs763877453 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015214 | GTATATAATGCTTAA[-/TT]TTTTGCACCAGGTAC | 55833 |
rs763893418 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968501 | AGCACTAATGGGACG[C/T]GGTACAAAGTCTCCA | 55833 |
rs763917282 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991379 | CAGCATAAAAGGAGG[G/T]GAGGCGGATTCCCAA | 55833 |
rs763961511 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022349 | GGTGGCATGCACCTG[C/T]AAGTCCCAGCTATTC | 55833 |
rs763990025 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048380 | TAGAGAGCGCATAAG[C/T]TGGGGCTATAACAGG | 55833 |
rs763995864 | snp | C/T | 9.8837e-05 | 0.00702914 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923918 | TGTGTGGTGGGTCTG[C/T]GATTGGCTCTGCTGT | 55833 |
rs764037824 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003056 | CCATTCTTTTCTTTC[A/G]TTGTTTTTTTTTTTC | 55833 |
rs764064607 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941424 | TACTACACGCATGCT[C/T]GGTTTTCTCCACAAA | 55833 |
rs764075407 | in-del | -/ATAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33990057 | CAAATCTAATCTACC[-/ATAT]ATATATATATATAAA | 55833 |
rs764075842 | snp | C/T | 3.29495e-05 | 0.00405877 | missense | UBAP2 | GRCh38.p7 | 9:33944505 | GACTGTCTCCAGGTG[C/T]TGATTCTCGAAGTTT | 55833 |
rs764121206 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948757 | ATTACTATGCAATGA[A/G]AACTGACTAAATAAA | 55833 |
rs764139529 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949726 | GTGTGCGCGCATGCA[C/T]GCGCACACACGCACA | 55833 |
rs764143921 | snp | G/T | 1.65045e-05 | 0.00287263 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933555 | TGTGGACGGCAGAAG[G/T]GCAGTGCAGGAGGTG | 55833 |
rs764150632 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929520 | GATGCTAAGATTTCC[-/T]TTTATGTATTGATGG | 55833 |
rs764170313 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042000 | ACTGCACTCCAGCCT[A/G]AGCAACAGACTGAGA | 55833 |
rs764202013 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013864 | CCTGGGCGACAGAGC[A/G]AGGCTCCATCTCAAA | 55833 |
rs764206921 | snp | A/G | 1.65004e-05 | 0.00287227 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986845 | ACCTCTAACTAGGGG[A/G]AAAAGAGCAGAAAAA | 55833 |
rs764217423 | snp | A/G | 3.56831e-05 | 0.00422377 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935696 | CCACAGCCAACACCT[A/G]GTCCAAAAACAAAAA | 55833 |
rs764220777 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020944 | TGGGATTACAGGACC[C/T]GGCCGGAATTCTGTT | 55833 |
rs764227584 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985503 | TAAAAGAATGAAATC[A/G]CGTCCTTTGGAGCAA | 55833 |
rs764282605 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987165 | CCTATAATTCCAGCA[C/T]TTTGGGAGGCTGAGG | 55833 |
rs764290600 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046957 | TGTTGTTCCAATATA[-/G]TTCTAAAGGCAACTC | 55833 |
rs764292665 | snp | G/T | 1.6486e-05 | 0.00287102 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953403 | CCCTGCTGTTGGGAA[G/T]TTTCAAAGGAGTTGG | 55833 |
rs764295754 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033240 | CAACAGGTGAATAGA[C/T]AAAACATGGTACTTA | 55833 |
rs764298263 | snp | C/G | 3.29451e-05 | 0.00405851 | missense | UBAP2 | GRCh38.p7 | 9:33923408 | TGCTGGCCATAACCA[C/G]TGGCCTGCTGGAAGG | 55833 |
rs764300500 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969735 | GCCAGGCATAGTGCC[A/G]GACACCTGTAATTCC | 55833 |
rs764311052 | snp | A/G | 1.67379e-05 | 0.00289287 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953487 | ATGCTAAGCAGACAA[A/G]AAGCAATGAGGAACC | 55833 |
rs764348058 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949997 | AAAAGACAATGGAAG[A/T]TCAACTACATTTTTA | 55833 |
rs764369452 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994924 | TGAGACTTCAATTAA[A/G]TCTGAACACTGACAC | 55833 |
rs764377623 | in-del | -/GG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033925 | ATTTTTAGTAGAGAC[-/GG]GGTTTCGTCATGTTG | 55833 |
rs764383624 | snp | G/T | 6.59141e-05 | 0.00574045 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941847 | GGTCATTGATAAAGA[G/T]GTATTCAAAGGCTCA | 55833 |
rs764396778 | snp | A/T | 1.648e-05 | 0.0028705 | missense | UBAP2 | GRCh38.p7 | 9:33943456 | CTGATGGGAATCTGA[A/T]TACTATTTTCACTGC | 55833 |
rs764432792 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923329 | AGGCAAGTGTGAGCC[A/G]GGCAAGCCTGTCTAA | 55833 |
rs764453728 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925640 | CAGTGGGGAGAAGCC[A/G]CTCCGCTCCCAGGCT | 55833 |
rs764458974 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034515 | GTTTTAATCCAAATA[-/C]AAAATTCCTTAATAA | 55833 |
rs764460362 | in-del | -/CT | 3.29595e-05 | 0.00405939 | utr-variant-5-prime, frameshift-variant | UBAP2 | GRCh38.p7 | 9:33996318 | CATCCTGATTTTTCC[-/CT]GTCACTTCCATAAGC | 55833 |
rs764492254 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930725 | ACATAGTGAAATCCC[A/G]TCTCTACTAAAAATA | 55833 |
rs764548490 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043676 | TTTTTACATTTTTTT[A/T]ATAGAGACAGGGTCT | 55833 |
rs764556387 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005957 | GGACTCTGGCCAGGC[A/G]TGGTGGCTCATGCCT | 55833 |
rs764575095 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989363 | CCTGCCACCACGCCC[A/G]ACTAATTTTTTGTAT | 55833 |
rs764604521 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035004 | CTATCTTGTAAGCAA[C/T]AACTACATAAACTGT | 55833 |
rs764607893 | snp | A/C | 1.65586e-05 | 0.00287733 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998869 | TCAGCTGTTGCCTGG[A/C]AAGTACATACAATTG | 55833 |
rs764624286 | snp | C/G | 1.64977e-05 | 0.00287203 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017052 | CACAAAAACTTACCT[C/G]TACCACTTGTTTCTG | 55833 |
rs764654697 | in-del | -/AAAAGGAAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005647 | AATTTTTTTCCTGTA[-/AAAAGGAAAT]AAAAGGAAATAAAAG | 55833 |
rs764665797 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931633 | TTATGATAAAAGATT[C/G]TGTGTAAGGTTTGAC | 55833 |
rs764684359 | snp | C/T | 3.32995e-05 | 0.00408027 | missense | UBAP2 | GRCh38.p7 | 9:33927012 | CAGGAAGCAGTCCTC[C/T]GGGACCTACGAGGTA | 55833 |
rs764684417 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941173 | TTAGCAAGAATCTAG[A/G]AGGGTAAAACTTTAA | 55833 |
rs764689907 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973230 | TCTCCCTCTGCCACG[C/T]CCAAATCCTTTAAAA | 55833 |
rs764707488 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964070 | AGAGTATTCTAATCT[A/G]TTCAACAGGTACCAG | 55833 |
rs764724706 | snp | A/G | | | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017078 | TTCTGTGGTTGCGTT[A/G]ATTGTGCTGCTGAAA | 55833 |
rs764733091 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952857 | TTTCTGGACTAAGAT[A/C]TACTGTAGAATTTTT | 55833 |
rs764740445 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976951 | TGGGAGGCAGCAGTC[A/G]CAGTGAGCCGAGATG | 55833 |
rs764748517 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015364 | CGCTCTGTTGCCCAG[A/G]CTTGAATGCAGTGGT | 55833 |
rs764759699 | in-del | -/TA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044993 | CCAATTCAATTATGC[-/TA]TATGTCCAGCATGAA | 55833 |
rs764764364 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928504 | AAACAGGAGGCTGAG[A/G]GAGGCCTTTGCTCCA | 55833 |
rs764780223 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948501 | GCCCAAACTCGGAGC[C/T]TTCAACTGGTCCAAA | 55833 |
rs764792845 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951307 | ACAGGGATGAGCCAC[C/G]ATGCCATGCCTGGCC | 55833 |
rs764826906 | snp | C/T | 1.65389e-05 | 0.00287562 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989093 | TTTCTTTTGCAAAAT[C/T]CTTTTTCTTACACCC | 55833 |
rs764841823 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | UBAP2 | GRCh38.p7 | 9:33948439 | GAAGTAGTAGTTGTA[A/G]GGTGACTTGTACTAT | 55833 |
rs764854863 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996702 | TGAGGTGGAACTATA[C/T]GAGTACACGGTCATC | 55833 |
rs764859224 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972173 | TTATATGCTCCTTTA[C/T]AGAAACATTAGATAA | 55833 |
rs764871886 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023672 | CTTTATTGTTTGGAA[A/G]AAGTTTTTCTCTTAA | 55833 |
rs764879034 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939994 | AGGAGGGAGGAGGGT[C/G]AGGAGGAGGGGAAAG | 55833 |
rs764885275 | snp | A/C | 0.000140875 | 0.00839152 | intron-variant | UBAP2 | GRCh38.p7 | 9:33938859 | GGTTTTTCTTGTTTC[A/C]GTGCCCATCTGTCAG | 55833 |
rs764904588 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932744 | CCCTAGCACAGGACC[A/G]GCTTCAGACCCATCC | 55833 |
rs764910960 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999663 | CAGCCTCCCAAAGTG[A/C]TGGGATTACAGGCCT | 55833 |
rs764937607 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938519 | AGCTTGTCATTGGCC[G/T]GGCGTGGTGGCTCAC | 55833 |
rs764968985 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989689 | TTCCCAACATAAAGC[C/T]CTTTCCTATGCAAAT | 55833 |
rs764979216 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983332 | GGATTCAACAGTGTA[C/G]TCAGTAGTGGGATTT | 55833 |
rs764990640 | in-del | -/ATTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991712 | CACTGAACAAACTCA[-/ATTT]ATTATGTTTGCTAAT | 55833 |
rs765018631 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971078 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCG | 55833 |
rs765043931 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936018 | TAATAAAGGGAAGAT[-/AAAC]AACAAACTCTCATGC | 55833 |
rs765047315 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922978 | CACCTGTGTCTTATT[A/G]TAGACAGAACCAGTC | 55833 |
rs765066593 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002798 | CCTCACGCACTCCAC[C/T]CCCCATAATTTCCCC | 55833 |
rs765084834 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973139 | ACTGCAGAATAAAAA[C/T]TAGGGAAGTAAATAA | 55833 |
rs765096791 | in-del | -/T | 3.30066e-05 | 0.00406229 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923066 | TGTTCCCCACAGCAG[-/T]TGTTCCCAGCTCCAG | 55833 |
rs765103736 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946939 | TTGGCTAATGTCTGA[A/G]AATTTGGACTGCTGG | 55833 |
rs765107582 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34035181 | TCTTTCTTCTGTTCT[A/C]ATTCTTTCATCTGTC | 55833 |
rs765126368 | snp | A/G | 3.30803e-05 | 0.00406682 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996211 | CAATGCAAATCAATT[A/G]ATAATACTTACTGTG | 55833 |
rs765139743 | snp | A/C | 5.46752e-05 | 0.00522825 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927747 | GGGACGCCAAGCAGG[A/C]ACCTTTGAGGGGCTC | 55833 |
rs765140708 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024494 | TGAAATGTTATAATA[C/T]CTAATTCCCTATTCA | 55833 |
rs765147278 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001781 | AAACCTAAAAAATGT[A/G]CCATACCAGCAGATT | 55833 |
rs765159746 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948292 | CTGGACAAATTCCAC[A/G]TTAGTCTTCACAAGT | 55833 |
rs765181112 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924087 | CAGGAACAGGTCTGG[C/G]TGCCAGCTCAGCACA | 55833 |
rs765184998 | snp | A/G | 5.31345e-05 | 0.00515407 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932655 | AACAGAGCGCCGTAT[A/G]TCCACCTGAACAAGT | 55833 |
rs765199995 | snp | G/T | 1.65509e-05 | 0.00287666 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923745 | CCCAGGTTTCCACCT[G/T]CCAGCAACCCAAGGC | 55833 |
rs765226089 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048074 | GGCAACTAATTAGAC[C/T]AAAAACTCAGGGGAA | 55833 |
rs765261709 | snp | A/C | 1.64795e-05 | 0.00287045 | missense, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33960859 | TGTTGTCCACTCTTC[A/C]ACAGAATTCTTCCAA | 55833 |
rs765268444 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007638 | TTTTGTCCTTGTATG[G/T]TTTATTTTTATTTTT | 55833 |
rs765278166 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944437 | GTGGACAGACACAGA[G/T]ATATTTTCAATGGTC | 55833 |
rs765287942 | snp | C/G | 2.13646e-05 | 0.00326831 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922495 | CCAGCCCACCCCTCT[C/G]TTCTGGGTTTAGTTT | 55833 |
rs765289369 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992257 | GCCGGGCGTGGTGGC[A/G]CATTCCTGTAATCCC | 55833 |
rs765317295 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960939 | TACAGTCTCAGTCCA[A/G]ATGATTCCTTTTTGT | 55833 |
rs765346859 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025533 | ACAGGTAAAGAACTG[C/T]TGCTACATTTTTAAC | 55833 |
rs765348260 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030973 | ATAAGGGCTAGGCAC[C/T]GTAGCTCCTGCCTAT | 55833 |
rs765355827 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998248 | ACAAATATTTTAAAA[A/G]TTAGCTGGGCATGGT | 55833 |
rs765366153 | snp | C/T | 3.295e-05 | 0.00405881 | missense | UBAP2 | GRCh38.p7 | 9:33944499 | TGGAGGGACTGTCTC[C/T]AGGTGTTGATTCTCG | 55833 |
rs765400841 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042479 | CAAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs765423187 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968483 | TTCAGGTTGGGACAT[C/T]TGAGCACTAATGGGA | 55833 |
rs765434865 | in-del | -/AA | 0.0526708 | 0.153497 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960781 | GTGAAATTCCATTTC[-/AA]AAAAAAAAAAAAAGA | 55833 |
rs765457958 | snp | C/T | 1.64944e-05 | 0.00287175 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33926629 | CACCACTGGCAGCCG[C/T]GACTGCAGCATCTGG | 55833 |
rs765468432 | snp | A/G | 1.6517e-05 | 0.00287372 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933538 | TCGCCAGTGTGCTGG[A/G]ATGTGGACGGCAGAA | 55833 |
rs765481904 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933684 | TTTCTAAAACCAATC[A/C]TAAGTGCCTGAAAAT | 55833 |
rs765488454 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966986 | GTAAAAACTAAATGT[C/T]ACAACAGTGGGACTA | 55833 |
rs765517486 | in-del | -/CAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930895 | AGTGAGACTGCATCT[-/CAAAAAAAAA]AAAAAAAAAAAAAAG | 55833 |
rs765520358 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923219 | CTGCAGACTTGTTTG[G/T]TGCCTGCGATGATCC | 55833 |
rs765524732 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020514 | TATTTTTAGTAGAGA[C/T]GGGGTTTGGCCATGT | 55833 |
rs765529940 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012055 | TGCATTAACTTTACA[A/T]ATTTTTTTCAGTTGA | 55833 |
rs765534905 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042322 | CTCTACCAAAAATAC[-/A]AAAAAATTAGCCAGG | 55833 |
rs765542026 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975608 | TCGAGACCATCCTGG[A/C]TAACACGGTGAAACC | 55833 |
rs765544204 | in-del | -/A | 3.49595e-05 | 0.00418073 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941913 | ACTTTAAATAGCTTC[-/A]ATAAAAAAAAAAAAA | 55833 |
rs765560370 | snp | C/G | 1.6492e-05 | 0.00287154 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953369 | TTGCGAATTTGTGAA[C/G]ACAAGGGCTTGGCCA | 55833 |
rs765583008 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005868 | ATGTCAATGAAAATA[C/T]ACCGTCCTTGAGAAT | 55833 |
rs765598552 | snp | A/G | | | utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34048930 | CAGGCTGCCCAACCC[A/G]TCACGTGACCTCGCG | 55833 |
rs765610508 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962308 | GACTTTTATACATGA[C/T]ATGTAGTAAGAATGG | 55833 |
rs765612515 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923311 | AGCGTGGCAGGGTAC[A/G]AGAGGCAAGTGTGAG | 55833 |
rs765651633 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930611 | GAATAAAAAGGGCAG[A/G]TGATGGCCGGGCGCG | 55833 |
rs765658855 | snp | A/C/T | 3.29491e-05 | 0.00405877 | missense | UBAP2 | GRCh38.p7 | 9:33941831 | AGTTCTGTACTGCAC[A/C/T]GGTCATTGATAAAGA | 55833 |
rs765678237 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965587 | AGGTTTCATGTTTAA[C/G]TGTAACCTTGGAGGG | 55833 |
rs765701943 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986890 | CCAAACCTCTTGTAC[A/G]TAACCTTATCAAGCA | 55833 |
rs765731369 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968489 | TTGGGACATTTGAGC[A/C]CTAATGGGACGCGGT | 55833 |
rs765733682 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041174 | AAGAAATCAACGGGC[C/T]GGGCACGATGGCTAA | 55833 |
rs765742186 | in-del | -/TCTG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014951 | TGAGTAGCAGAGATA[-/TCTG]TCTGTTAATACCAGC | 55833 |
rs765761660 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019057 | AACACATGCTACCAC[A/G]TGGATGCACCTCAAA | 55833 |
rs765763540 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032162 | GTGCTAATAAGTTGC[C/T]AACTTAACATCCTCA | 55833 |
rs765789145 | snp | A/G | 1.66832e-05 | 0.00288814 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943406 | GCTTCATAACAAAGG[A/G]CTAAATTCAGTACCT | 55833 |
rs765829760 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942848 | ATCCCTCATAGACTA[C/T]TGGTAGGAATGTCAA | 55833 |
rs765832848 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992671 | GGAGGGGGGGGGGCA[A/C]AAATAGGGAAAAGAA | 55833 |
rs765846717 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027208 | GGCCAAGGCCAGGTA[C/T]GGTGGCTCACACCTG | 55833 |
rs765847221 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932403 | CAGATGGTGCCCAGG[-/A]AATCAGAAGCTCGAA | 55833 |
rs765847958 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944065 | TGATGAAAGTATCAC[C/T]TGGTCAAGGAACCAT | 55833 |
rs765854334 | snp | C/T | 3.29712e-05 | 0.00406011 | missense | UBAP2 | GRCh38.p7 | 9:33927884 | TGTTCGCGGTGTTCA[C/T]GCTACTGGACAGGCT | 55833 |
rs765859262 | snp | A/G | 0.0256002 | 0.110203 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017018 | AAAAGAAAAAAAAGG[A/G]AAAAAAAAAAAAGAG | 55833 |
rs765869013 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994243 | TCCTTCAGGTTCGGT[C/T]CCAAAGGAGGAGGGG | 55833 |
rs765881481 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989507 | CGCCCGGCACATGCA[C/G]GTATCTTTCAAACCT | 55833 |
rs765907946 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930394 | ATCAAGACTGAAAAC[G/T]ACCCTAAATGGACGG | 55833 |
rs765909039 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989420 | GTTAGCCATGATGGT[C/T]TCGATCTCCTGACCT | 55833 |
rs765912416 | in-del | -/TAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999895 | ATGTATGTATGTATG[-/TAT]GTATGTATGTTATTT | 55833 |
rs765922005 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993179 | AAAAACATCATGGAC[A/G]ATTCCACTTAACACC | 55833 |
rs765946025 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963974 | GAATCTTATCCTTGA[C/T]GGCTCTTGGACACTC | 55833 |
rs765949922 | snp | A/C/G | 0.000131789 | 0.00811661 | missense | UBAP2 | GRCh38.p7 | 9:33923944 | GCTGTGGCTGAGCTG[A/C/G]TGTGGTAGCGGGTGC | 55833 |
rs765965349 | snp | A/C/G | 8.23725e-05 | 0.00641722 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971710 | AGCTTTGTCCCACAC[A/C/G]CATCTGTAGATGTAG | 55833 |
rs765967691 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014093 | CTTGGGAGATCAAGG[C/G]GGGGACAGATCACTT | 55833 |
rs765994708 | in-del | -/AG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973413 | CAACTACCTATACCC[-/AG]AGTTAGTGACTTCTA | 55833 |
rs765998668 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982476 | GCTTTTATATAAAGC[A/G]AACGTAATAGATTTT | 55833 |
rs766016402 | snp | A/G | 1.80322e-05 | 0.00300262 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922783 | GGGTGCATAGCCAGG[A/G]GCCGCTCCCGAGGCC | 55833 |
rs766017435 | snp | A/T | 1.84004e-05 | 0.00303313 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944683 | GCATAATGGCTTCAC[A/T]ATGTTCTTCAATAGA | 55833 |
rs766017677 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949850 | ATAGACACTGCTATT[C/T]TCATTTCAAGTTGTT | 55833 |
rs766033788 | snp | A/G | 6.60775e-05 | 0.00574755 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948408 | GGACTGGGATGTTGG[A/G]GGCTTGAGGTCCCAA | 55833 |
rs766037442 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007218 | CTCAAGTGAGGCCAG[A/G]TGCAGTGACTCACGC | 55833 |
rs766075065 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951255 | TTCCTGGCATCTCAT[A/T]ATCTTCCAGCCTCAG | 55833 |
rs766112021 | snp | C/T | 0.00270736 | 0.0366927 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924019 | GGAAAGAGCACTGAC[C/T]CCAGCCACTGCCCTT | 55833 |
rs766113919 | snp | C/G | 1.64806e-05 | 0.00287054 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935795 | CCTCTTCCTCTGTTT[C/G]GTTGGCACCAGCCAT | 55833 |
rs766129101 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945456 | AGTGAGCTGAGATGG[C/T]GCCACTGCACTCCAG | 55833 |
rs766142271 | in-del | -/AGCAGTTGTTCCCCAC | 3.29755e-05 | 0.00406038 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923045 | ACTCCTAGGAGGAAA[-/AGCAGTTGTTCCCCAC]AGCAGTTGTTCCCAG | 55833 |
rs766150901 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043298 | AACCTCAGCCTCCTG[A/G]GTAGCTGGGACTACA | 55833 |
rs766174121 | in-del | -/TA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976846 | ACTAAAAAAAATGTA[-/TA]TATATATATACAAAA | 55833 |
rs766208761 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939282 | CACTGCAACCTCCTC[C/T]GCCTCCCAGGTTCAA | 55833 |
rs766223223 | in-del | -/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921990 | AGATGAAGATTTGGT[-/G]GAAGGAGACCATGAC | 55833 |
rs766226265 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959661 | GACTGACAGTACCCA[C/G]AAGCTAGTGTAACAT | 55833 |
rs766258199 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004357 | AAGTGTGGTGGTAAG[C/T]GCTGTAGTCCCAGCT | 55833 |
rs766273640 | snp | G/T | 1.64852e-05 | 0.00287094 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935901 | GAAAAGAAGAGAAGA[G/T]AATATAAACTTACAA | 55833 |
rs766274245 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958027 | ACATGATCACTGAGG[C/T]TCACTGCAGCTACAA | 55833 |
rs766286254 | snp | C/T | 1.66721e-05 | 0.00288717 | missense | UBAP2 | GRCh38.p7 | 9:33927029 | GGACCTACGAGGTAC[C/T]GGTTGTGCAGCAGGG | 55833 |
rs766296720 | snp | A/G | 0.000220307 | 0.0104931 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926959 | AGGCCAGGGGAGCTG[A/G]GCAGGCCAGGAGTTC | 55833 |
rs766306858 | snp | A/G | 3.29679e-05 | 0.00405991 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923512 | GAGGTATTAGTGTAG[A/G]AAGAGGCAAGCTGAG | 55833 |
rs766308816 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009907 | CCGCCTCCTGGGTTC[A/G]AGAGATTCTCCTGCT | 55833 |
rs766309642 | in-del | -/CGAGGC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978531 | AATCCTAGCACTTTA[-/CGAGGC]CGAGGCCAAGGCAGG | 55833 |
rs766356415 | snp | A/T | 1.64792e-05 | 0.00287042 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989064 | CTTCTCTCTATTCTC[A/T]TTGTTTTCTGAATTT | 55833 |
rs766400127 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | UBAP2 | GRCh38.p7 | 9:33923455 | GAGGTTCACCCCATG[A/T]TGCTTGGCTGAGGCT | 55833 |
rs766411093 | snp | C/T | 1.6686e-05 | 0.00288838 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944314 | CCCACTAGAGCTGAA[C/T]GTAAAAATAATTCCA | 55833 |
rs766437873 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996903 | GACAATATAGTGAGA[A/C]CTCATCTTTACAAAA | 55833 |
rs766453088 | in-del | -/TTTTTTTTCTTTTGTTTTTTTTTTTTTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33939201 | GTCTTTTTTTTTTTT[lengthTooLong]TTTTTTTTTTGAGAT | 55833 |
rs766468665 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972084 | TGAGAGTCCTGCTGA[A/C]AAATAAGGCATAAAT | 55833 |
rs766480842 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046974 | TCTAAAGGCAACTCC[A/G]TGTGACTACTGCTGA | 55833 |
rs766481766 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992160 | TTTGGGAGGCTGAGC[-/G]GGTGGATCACCTGAG | 55833 |
rs766493661 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044938 | CTACTCCTTAATGTG[A/G]GCCCTATTTCATACT | 55833 |
rs766494599 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002597 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 55833 |
rs766503670 | snp | G/T | 1.65803e-05 | 0.00287922 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33932565 | GCAGACACTTACTGT[G/T]TGTGACGTGCTCGAG | 55833 |
rs766506485 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024162 | TCGGGAGTTCAAGAC[C/G]AGCCCGACCATCTCT | 55833 |
rs766548353 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978471 | TCATGCAATAATTAG[C/T]TTTAAAAGTAGAGGA | 55833 |
rs766563675 | snp | C/T | | | stop-gained | UBAP2 | GRCh38.p7 | 9:33922514 | TGGGTTTAGTTTGTC[C/T]AGTATGGAGAGTTGC | 55833 |
rs766570740 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989574 | TAAATTCTTTCCCTA[C/T]AGTTCTACTTTATTG | 55833 |
rs766571912 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020817 | GGCACCCGCCACCAA[A/G]CCCAGCTAATTTTTT | 55833 |
rs766579325 | in-del | -/TTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994464 | ATTCCCAAAGATTTT[-/TTC]TTTTTTTTTTTTTTC | 55833 |
rs766590716 | snp | A/C | 4.73373e-05 | 0.00486481 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922489 | CTTGCCCCAGCCCAC[A/C]CCTCTCTTCTGGGTT | 55833 |
rs766608739 | snp | C/G | 1.64817e-05 | 0.00287064 | missense | UBAP2 | GRCh38.p7 | 9:33960850 | CCAGTCTTCTGTTGT[C/G]CACTCTTCCACAGAA | 55833 |
rs766610528 | snp | A/G/T | 0.000312979 | 0.0125058 | missense | UBAP2 | GRCh38.p7 | 9:33944426 | GGCTGTGGCTGGTGG[A/G/T]CAGACACAGAGATAT | 55833 |
rs766612653 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977227 | TATTTTTATTAGAGA[C/T]GGGGTTTCACCATTT | 55833 |
rs766649962 | in-del | -/GAGT | 7.49653e-05 | 0.00612185 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927126 | AATGGTCACCACAAA[-/GAGT]GAGAGTCCTCAGCTG | 55833 |
rs766656080 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041298 | GCTCTACTAAAAATG[-/C]AAAAAAAAAAAAAAA | 55833 |
rs766658366 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982369 | TCTGCTCCACACTTA[A/C]GACAACTTACTATCC | 55833 |
rs766659230 | snp | A/G | 3.29957e-05 | 0.00406162 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973260 | AAAACACACAATTAT[A/G]GTATAAAATAATACT | 55833 |
rs766659900 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923121 | GGGGTTGCCCTGCCT[A/G]AGAGGGGATCAGGCA | 55833 |
rs766669383 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985383 | TTTTGAAGTGAAGCA[C/G]TATTCACAATATTCA | 55833 |
rs766691376 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984325 | TCAGACAATACAAGG[A/G]ATCTAAACAACTCAA | 55833 |
rs766703712 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986726 | CTTCTTCCCCCTAAT[C/T]GAAAGCATTTTCTTC | 55833 |
rs766726951 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029263 | CCAGGCGTAGTGGCT[C/T]AGACCTGTAATCCAG | 55833 |
rs766730441 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969065 | ATATTTTGCTTATAC[A/G]TTCATCCATTGATAA | 55833 |
rs766774560 | in-del | -/GT | 1.64727e-05 | 0.00286986 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33941765 | GACTAGCAGAATTCA[-/GT]GATGAGCTTGTCAGA | 55833 |
rs766782132 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007694 | CCCAGGCTGGAGTGC[A/C]GTGGAGTGATCTCGG | 55833 |
rs766843187 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968172 | ATAGAAGAAGAAATC[C/T]ACTGGGTTTTGGGAT | 55833 |
rs766846461 | snp | A/G/T | 3.29583e-05 | 0.00405934 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923017 | TAGACCAGTGGTGCT[A/G/T]GAAGACACTGATACT | 55833 |
rs766891299 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047946 | CAATATCCAATAGAA[A/G]TGGTAGTAAATGACT | 55833 |
rs766891807 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947584 | CTCAGCACTTTTGGA[A/G]GCCGAGGTGGGCAGA | 55833 |
rs766915378 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981921 | AATAATGTCAGAATC[-/AT]AGTAATTTTCACATT | 55833 |
rs766924845 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954047 | GAGTAGCTGGGATTA[C/G]AGGCGTGTGCCACCA | 55833 |
rs766925164 | snp | A/G | 0.000329832 | 0.0128377 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953358 | TGATTGTTGTGTTGC[A/G]AATTTGTGAAGACAA | 55833 |
rs766940686 | snp | C/G | 3.295e-05 | 0.00405881 | missense | UBAP2 | GRCh38.p7 | 9:33923191 | TAAACACTACCTTTG[C/G]CAGGCCCAGAACCTG | 55833 |
rs766979483 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995346 | TGGGTGGCAGAGTGA[A/G]GCTGTCTCAAAAAAA | 55833 |
rs766980075 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049380 | CTTCTAGACGAACCC[C/T]CTAGAGACCTTAGAG | 55833 |
rs766980911 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042955 | TCCCTGTGGTCCAAG[A/C]TACTCAGGAGGCTGA | 55833 |
rs766990215 | snp | A/G | 1.8712e-05 | 0.0030587 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953245 | CATTTGCTAATGGGT[A/G]TATTTCTTAAAATCC | 55833 |
rs767002926 | snp | C/T | 1.74732e-05 | 0.00295572 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927798 | TCTGGAGCAAATACC[C/T]GAGGTCACCAAGGGC | 55833 |
rs767042603 | in-del | -/TTC | 3.16321e-05 | 0.00397681 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963688 | AAGCAATTTATAAGA[-/TTC]TTAATTTTAAAAATT | 55833 |
rs767061006 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025893 | TTTAACTGCTGTTTT[C/T]TTCAAGGACCTTTCT | 55833 |
rs767066443 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038975 | tgcccgaccgcgacc[C/T]cgtctgggagttgag | 55833 |
rs767072874 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961251 | TGGTTTGATTTCTTC[C/T]GATATAGTCTTCAAA | 55833 |
rs767073474 | snp | C/T | 1.6686e-05 | 0.00288838 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998738 | TTATCTTTTTAAGCA[C/T]AATCAAAATAGATTA | 55833 |
rs767083775 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031277 | GCAAAACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs767086185 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | UBAP2 | GRCh38.p7 | 9:33941810 | TGACGGAAGTTGTAT[A/G]TGTGGAGTTCTGTAC | 55833 |
rs767092014 | snp | C/T | 1.64898e-05 | 0.00287135 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963786 | TGTGAGTATTTGATG[C/T]CAGTTCTGTGGACCA | 55833 |
rs767117217 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965756 | AGCAGTTCTTAAAAT[C/G]AGGGAGTGTGGGCCG | 55833 |
rs767130194 | snp | C/G | 1.64735e-05 | 0.00286993 | missense | UBAP2 | GRCh38.p7 | 9:33923924 | GTGGGTCTGTGATTG[C/G]CTCTGCTGTGGCTGA | 55833 |
rs767143460 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993054 | CGATACTTCAAAACA[A/G]TTTTGTCACATCAAC | 55833 |
rs767183533 | snp | A/G | 3.29658e-05 | 0.00405978 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971653 | ACAGAACACTTACCA[A/G]TTCCCTCATCTGCAC | 55833 |
rs767226746 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993492 | ACATAGAAACACAGA[A/G]ACCCCCTAACTCTAC | 55833 |
rs767228813 | snp | A/G | 1.80869e-05 | 0.00300718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922673 | AGGGTGGCTGCCTCC[A/G]TCACTGTACTCACCT | 55833 |
rs767241227 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014051 | AAAAGGGCCAGGTGC[A/G]GTGGCTCACACCTGT | 55833 |
rs767245615 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003971 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 55833 |
rs767270790 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930490 | AAAAACCCTTAAGTT[G/T]CAACATGGAAACATC | 55833 |
rs767278693 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924004 | TTGTGACATCACCTA[C/G]GAAAGAGCACTGACT | 55833 |
rs767287856 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950774 | CTATGTGCTTTACAA[C/T]ACAGCGAAATCACTG | 55833 |
rs767299579 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951022 | TGCTGCTGTTATTTA[A/C]TAGGTTCATTATTAA | 55833 |
rs767370789 | snp | C/G | 1.80507e-05 | 0.00300417 | missense | UBAP2 | GRCh38.p7 | 9:33922773 | GGAATGGTGGGGGTG[C/G]ATAGCCAGGGGCCGC | 55833 |
rs767389517 | snp | C/T | 3.30049e-05 | 0.00406219 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33988991 | CTCTGCCACGATTGC[C/T]GCCTCTTCCTTTCCG | 55833 |
rs767395838 | snp | A/C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969873 | CCTCAAACACCCCCC[A/C/G]ACCCCCAAAAAAAAC | 55833 |
rs767411734 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000475 | CCGTAATTATTACAA[C/T]AGGGAAATTAGGTGA | 55833 |
rs767440703 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022343 | GGGCAAGGTGGCATG[C/T]ACCTGTAAGTCCCAG | 55833 |
rs767454883 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931796 | TGCCTCCTCCATTCG[C/T]CTGCACCCTAATCCT | 55833 |
rs767470144 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026926 | CTTCTATACAACAGC[A/G]TAACTATTGTTGGCA | 55833 |
rs767472712 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050605 | TGGTGGCTCACACCT[A/G]TAATCTCAGCACTTT | 55833 |
rs767483060 | snp | C/T | 3.20971e-05 | 0.00400593 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935706 | CACCTGGTCCAAAAA[C/T]AAAAAAGCAAAAGGG | 55833 |
rs767514151 | in-del | -/A | 1.64885e-05 | 0.00287123 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926570 | AGAGGGGGGACATGT[-/A]AAAAGATTCTGAACC | 55833 |
rs767528070 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036558 | TGGAATCCTATACAC[A/C]CATTTAAACTGTGTG | 55833 |
rs767532509 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982239 | CATTCTAATAATTCC[A/G]CTTCAACCCAAATCC | 55833 |
rs767545516 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946717 | CAGAATTTAATTTAA[A/G]AAAAAACAAATGGCA | 55833 |
rs767546984 | snp | A/G | 5.05557e-05 | 0.00502745 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953498 | ACAAAAAGCAATGAG[A/G]AACCAGTCATAAGCA | 55833 |
rs767561774 | in-del | -/ACAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961716 | GGAGTTAATCATCTG[-/ACAA]ACAAAATTCCATTTC | 55833 |
rs767610390 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001362 | TATTAGAAAAAGAAA[C/T]GTGACCTATTGTTTT | 55833 |
rs767635866 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034829 | AGTGAGTCAAGATCA[C/T]GCCACTGCACTCCAG | 55833 |
rs767656406 | in-del | -/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994711 | TTGTCTTGTGTACCA[-/G]GTGTTCTCTTACATG | 55833 |
rs767660251 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957831 | TGTAAGCAGGAGGTA[A/G]AGGAGACAGTAGGTG | 55833 |
rs767660425 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030123 | CTGGGCAACATAGAG[-/A]GAACCCGTCTCTATA | 55833 |
rs767660710 | snp | A/G | 9.88354e-05 | 0.00702908 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923335 | GTGTGAGCCAGGCAA[A/G]CCTGTCTAACCCCAT | 55833 |
rs767661963 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959882 | AGCTGGCTATCAGGT[C/G]AAACAAAACACAGAT | 55833 |
rs767664485 | snp | C/G | 6.80747e-05 | 0.00583376 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926947 | TGCCAGCCCCCGAGG[C/G]CAGGGGAGCTGGGCA | 55833 |
rs767671678 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045058 | TGTTTACAAACGGGT[-/A]AAAAAAAGGCTGGGC | 55833 |
rs767685643 | snp | C/T | 1.64754e-05 | 0.00287009 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989053 | TTCTCGCTTTTCTTC[C/T]CTCTATTCTCTTTGT | 55833 |
rs767691937 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023519 | ATGTTCACAGTATCA[A/G]CATTAAGACTATATC | 55833 |
rs767709169 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943470 | ATTACTATTTTCACT[A/G]CTTGGAGCTGATCCA | 55833 |
rs767710804 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046909 | ACTACATAGACTGCA[C/T]TAGTAACCAGGAAAG | 55833 |
rs767712732 | snp | C/T | 3.09631e-05 | 0.00393454 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922479 | CAGGATAAGCCTTGC[C/T]CCAGCCCACCCCTCT | 55833 |
rs767739908 | snp | A/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922018 | GACAGATGACAAACG[A/G]AACAGTTTCTCAAAA | 55833 |
rs767743660 | snp | C/G | 1.67539e-05 | 0.00289425 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943623 | CGTGTCAGGAACAGA[C/G]GTCACAGATTCCAGG | 55833 |
rs767804584 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954002 | ACCTCTGCCTCCCAG[C/G]CTTAAGCGATTCTCG | 55833 |
rs767812111 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017060 | CTTACCTGTACCACT[C/T]GTTTCTGTGGTTGCG | 55833 |
rs767816528 | in-del | -/A | 1.6483e-05 | 0.00287076 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923165 | CAGGCCTTATCCTGG[-/A]AAAGGAGAGGTAAAC | 55833 |
rs767817603 | snp | A/G | 3.31774e-05 | 0.00407279 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932550 | GGAAGAGGAAGCCGC[A/G]CAGACACTTACTGTG | 55833 |
rs767821497 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996797 | TTTGGATTAGAACAC[G/T]TCAAAGGCCAGCCGC | 55833 |
rs767821918 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923433 | GGAAGGGAGGTGTGG[G/T]AGTGCTGAGGTTCAC | 55833 |
rs767844114 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948263 | TGCAAGAGTTCTACT[A/C]AAAAGAAACATCTCT | 55833 |
rs767874985 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997756 | TGGGCCAGTGTTCTA[C/T]CTATACTATTCAGAT | 55833 |
rs767875134 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983410 | CAGAAGCATGTGAGA[A/G]ATCAAATACCCTAGG | 55833 |
rs767876597 | snp | C/T | 1.64827e-05 | 0.00287073 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924174 | GCGCTAGGCCGGCCC[C/T]GGGCTACTCCTCATC | 55833 |
rs767952679 | in-del | -/AATT | 1.65756e-05 | 0.00287881 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998880 | CTGGAAAGTACATAC[-/AATT]GTTAAGGATTTGAAC | 55833 |
rs767966601 | snp | A/G | 1.68218e-05 | 0.00290011 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922906 | GAAGACAATGGTGAA[A/G]GTCAGGTTGGGCTGT | 55833 |
rs767979446 | snp | C/T | 0.000122849 | 0.00783642 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932647 | GAAGACAAAACAGAG[C/T]GCCGTATGTCCACCT | 55833 |
rs767981745 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923592 | CAACCACAGGGGACC[C/T]GTGTTTTCATTAGTG | 55833 |
rs767983180 | snp | A/G | 1.64985e-05 | 0.0028721 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924312 | AGGGAGGCTTGATCA[A/G]CGACTGGCCCTGCTT | 55833 |
rs768041029 | snp | A/T | 1.64874e-05 | 0.00287113 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973157 | GGGAAGTAAATAATT[A/T]TAAAAATAGGATGGC | 55833 |
rs768070935 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923175 | TCCTGGAAAGGAGAG[A/G]TAAACACTACCTTTG | 55833 |
rs768074729 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974118 | ATCCATGAGCCCAGG[A/G]GTTGGAGGTTGCAGT | 55833 |
rs768121230 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33952948 | GATCATGGCTCACTG[A/C]AACCTCAAACTCCTG | 55833 |
rs768122550 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994366 | TAAAGGAAAGGCAAC[-/A]AAAAAATAGTGTCTG | 55833 |
rs768127613 | snp | C/T | 8.23703e-05 | 0.00641704 | missense | UBAP2 | GRCh38.p7 | 9:33924238 | GCTAGGCTCCCATCT[C/T]GGCTGGCAAGCGCTG | 55833 |
rs768131168 | snp | A/T | 3.2969e-05 | 0.00405998 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973242 | ACGTCCAAATCCTTT[A/T]AAAAAACACACAATT | 55833 |
rs768135214 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965310 | GGGTTGTTTTCTTAT[G/T]ACTGAATTGTGAGAG | 55833 |
rs768139883 | snp | A/G | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921789 | GAATGGAGATGTGTT[A/G]CTTGGAGATACCTTA | 55833 |
rs768147653 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | UBAP2 | GRCh38.p7 | 9:33948539 | AGCTGGTGATGTTTG[C/T]CATTTTTGGTGGTGC | 55833 |
rs768148511 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963810 | TGGACCAATGTAAAA[C/T]TGAGGGTTTAAACAT | 55833 |
rs768163891 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986716 | CAACTGCCTGCTTCT[C/T]CCCCCTAATTGAAAG | 55833 |
rs768173434 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999286 | ATTAGCCTGGGCAAC[-/AT]AGAGAGACCCTGTCT | 55833 |
rs768183693 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976373 | AACATTAAGTTAATC[A/C]CTTCAGGGTAAAGGC | 55833 |
rs768188274 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966839 | ATTCATCCTCTGTAC[C/T]TCTAAAAAGGGGAGA | 55833 |
rs768190911 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026277 | CAAAGCATTGATTGG[A/G]AGATAGTTCTAAAAC | 55833 |
rs768202555 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030721 | CACAAGGTCAGGTGA[C/T]CGAGACCATCCTGAC | 55833 |
rs768233694 | snp | A/G | 8.24436e-05 | 0.00641989 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926595 | TGAACCCTCTGCTCC[A/G]ACCAGTCCATACCCC | 55833 |
rs768233764 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941930 | TAAAAAAAAAAAAAC[-/AT]AAACAGCTTCACGAG | 55833 |
rs768259164 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023958 | CTGACGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 55833 |
rs768325428 | snp | G/T | 1.6476e-05 | 0.00287014 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986796 | CACGATCTGAAGGTT[G/T]GTCCACTTGATTGCA | 55833 |
rs768334937 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999958 | TGGAGTATTTATTTA[C/T]TTATTTTGAGATGGA | 55833 |
rs768341257 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985229 | ACATAATATTTAAAC[A/T]AATTTATGGGGTACA | 55833 |
rs768383545 | in-del | -/AAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040325 | TGAGACTCTGTCTCA[-/AAAAA]AAAAAAAAAAAAAAA | 55833 |
rs768391467 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923280 | TGCTGTCCCCTGGGT[C/G]AGGTCGTCATAACCT | 55833 |
rs768410950 | snp | G/T | 0.00844826 | 0.0644419 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988923 | GCTGAGGCGGGAGGG[G/T]CACTTGAGATGAAAG | 55833 |
rs768413108 | snp | C/T | 3.29913e-05 | 0.00406135 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953349 | GGTGCCATCTGATTG[C/T]TGTGTTGCGAATTTG | 55833 |
rs768414118 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983561 | AATCACACACATAAC[A/G]TTGGTCTTATACTGT | 55833 |
rs768427425 | in-del | -/AAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962649 | CTCTATCTCAAAAAT[-/AAAT]AAATAAATAAATAAA | 55833 |
rs768429449 | snp | C/G | 1.64955e-05 | 0.00287184 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953431 | TGGCTTCTGAGGCTT[C/G]ACTGTGAGGAACAGG | 55833 |
rs768436569 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925053 | ATACAACAAAGTGTG[A/G]AGACAGAGACGGCAA | 55833 |
rs768455162 | snp | C/T | 1.6519e-05 | 0.00287388 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927926 | ATGCGGAACTTGAGA[C/T]GGAGGTCGCTGCCGT | 55833 |
rs768458652 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992983 | CTTTGCCTTTGCCAA[A/G]AACTACCAACACAAA | 55833 |
rs768488842 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956254 | TTACACTTCGCATAA[C/T]AGCTATTCTAAAGAA | 55833 |
rs768524971 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044773 | CAGGAGGCTGAGGCA[A/G]GAGCATCACTTGAAC | 55833 |
rs768532895 | in-del | -/A | 4.96956e-05 | 0.00498451 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948603 | CTTTAAAAGGGGGAT[-/A]AAAGAACAAATCCTC | 55833 |
rs768540504 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960762 | TCCAGCCTGGGCAAC[A/G]AAAGTGAAATTCCAT | 55833 |
rs768541371 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950789 | CACAGCGAAATCACT[C/G]AATCAATGACTACTG | 55833 |
rs768549732 | in-del | -/AGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016271 | AGGAAGAGGAGGAAG[-/AGA]AGGAGGAAGAGGAGG | 55833 |
rs768643997 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923987 | GTCCCCACGGCCAAA[C/T]TTTGTGACATCACCT | 55833 |
rs768650946 | snp | A/G | 1.68055e-05 | 0.0028987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926976 | CAGGCCAGGAGTTCC[A/G]CCATACACTCACCGG | 55833 |
rs768662520 | snp | C/T | 1.80716e-05 | 0.0030059 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922762 | CAAGATGTGTAGGAA[C/T]GGTGGGGGTGCATAG | 55833 |
rs768703902 | snp | C/T | 1.88934e-05 | 0.00307349 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928016 | AGAAAAGCCAGGACA[C/T]ATGGATCTGGAGGCA | 55833 |
rs768730731 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014984 | CAGAATACTACACTA[A/G]CTTTATACTGAAAAA | 55833 |
rs768745038 | snp | A/G | 1.6708e-05 | 0.00289028 | missense | UBAP2 | GRCh38.p7 | 9:33948386 | TACCAAGATGACTGA[A/G]GACTGAGGACTGGGA | 55833 |
rs768765434 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967520 | TTGTTTGTTTTTAAT[C/T]AGAAAAATTATTTAT | 55833 |
rs768774329 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045170 | GCTAACACTGTGAAA[-/C]CCCGTCTCTAATAAA | 55833 |
rs768841880 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994441 | GAACAATTTGGGTTA[C/T]TTTGTTTATTCCCAA | 55833 |
rs768879888 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932134 | TAAAGCTGGCGCGCC[A/G]ACTCCAGCCCTCCTG | 55833 |
rs768919924 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970649 | ATGTTAACCAGGCTC[A/G]TCTCAAACTCTGGCT | 55833 |
rs768922446 | snp | A/G | 0.000116896 | 0.00764422 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996175 | TTGAAAATGTGCTAC[A/G]GAATTGGAGACAAAT | 55833 |
rs768931748 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991398 | GCGGATTCCCAAAAT[A/G]TCAAATTCAGGAGAC | 55833 |
rs768966490 | snp | A/G | 3.29755e-05 | 0.00406038 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935771 | TGTTTTCCACATCAC[A/G]TGAGCTATCCTCTTC | 55833 |
rs769014918 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947435 | TCTACACATGGGACC[C/T]TTACAATACAAACCA | 55833 |
rs769029311 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002136 | TTGTTGTTATTTTCA[C/T]AAAGACAAGGTCTCA | 55833 |
rs769046026 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945945 | TAGGATCAACTGGTA[A/G]GATAAAGTTGCCCCT | 55833 |
rs769054417 | snp | A/G | 3.30972e-05 | 0.00406786 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926714 | ACATACCACACCCTG[A/G]GAAGCCCAGGTCCAT | 55833 |
rs769067015 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938498 | AACTTATGTTGAAAC[A/G]AAAACAGCTTGTCAT | 55833 |
rs769141068 | snp | C/G | 1.65018e-05 | 0.00287239 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960810 | AGAAAGGTCTCATCT[C/G]ACAGCAAACACTTAC | 55833 |
rs769142062 | snp | A/G | 3.41764e-05 | 0.00413364 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932632 | CTGGAGAGCGAACTA[A/G]AAGACAAAACAGAGC | 55833 |
rs769158158 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33954965 | TTCAAAGGTGTTTAG[C/T]GTGAAAACTAGAATA | 55833 |
rs769159445 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | UBAP2 | GRCh38.p7 | 9:33944387 | GCTGGGGGTATCCGC[C/T]GCTTAGCAAGTTTGA | 55833 |
rs769184821 | in-del | -/TA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982540 | ATAGTTTAAATGGAC[-/TA]TATGTTTTTGATTGT | 55833 |
rs769201564 | in-del | -/GAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992657 | ACAACTTATCGGGCG[-/GAG]GGGGGGGGGCACAAA | 55833 |
rs769273328 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988603 | CCTTCTTTGCCACAC[A/G]CACACCATTCTAAAA | 55833 |
rs769274274 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034922 | CAACTGTTCTCTACA[A/T]CCGGATTACTCTCAA | 55833 |
rs769282733 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942974 | GAACTGAAAGCATGC[A/G]AAACTTGAAACCAAA | 55833 |
rs769305576 | snp | G/T | 8.23689e-05 | 0.00641698 | missense | UBAP2 | GRCh38.p7 | 9:33924215 | ACTCACCTGGATATG[G/T]ATTATTAGCTAGGCT | 55833 |
rs769308381 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998428 | TTTTAAAGGTAATTC[A/T]GTTCATCTCTAACAT | 55833 |
rs769386898 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979965 | GTAGTCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 55833 |
rs769391241 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967723 | AAATCAGAAATGTCA[C/T]CTCCAAAAACAAGTT | 55833 |
rs769420254 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005592 | GGAATATAAAACTTA[A/C]CAATTAATGTCTCAA | 55833 |
rs769423853 | snp | A/G | 3.3071e-05 | 0.00406625 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953319 | GAGTTGACGGCAGTG[A/G]AGCTGCCAGTCCCTG | 55833 |
rs769450477 | in-del | -/G | 2.41193e-05 | 0.00347262 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935718 | AACAAAAAAGCAAAA[-/G]GGGCTGCTTTTTAAC | 55833 |
rs769462491 | snp | A/G | 1.67214e-05 | 0.00289144 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933497 | CCCCATACCTGCTAA[A/G]CTGAGAGAGAGGGCT | 55833 |
rs769478393 | in-del | -/GAGGGAGAGGGAAGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940026 | GAGGGGGAGGGAGAG[-/GAGGGAGAGGGAAGA]GAGGGAGAGGGAAGA | 55833 |
rs769500053 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030483 | AAAAAACTGGCCCGG[C/T]ATGACAGAGCACACC | 55833 |
rs769508309 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978728 | GAGCGTGCAATGAGC[A/C]GAGATTGTGCCACTG | 55833 |
rs769537010 | snp | C/G | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921546 | CCATTGTGATTTGGG[C/G]CAAGAGGGTCCAGTA | 55833 |
rs769552411 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | UBAP2 | GRCh38.p7 | 9:33924278 | CAAAGGGAATTCCAT[A/G]GTAGTCCTAGGAGAG | 55833 |
rs769557491 | in-del | -/TACG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999851 | AGTAGCTGGGATTAC[-/TACG]TATGTATGTATGTAT | 55833 |
rs769572250 | snp | A/G | 6.58989e-05 | 0.00573978 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33986785 | GGCTCGCTTGCCACG[A/G]TCTGAAGGTTTGTCC | 55833 |
rs769607620 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048293 | GAAAACTGAGTCCCA[A/G]TTGAGACCAATGCCC | 55833 |
rs769615972 | in-del | -/TTG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966751 | ATTCTTTGTTTGCAA[-/TTG]TTCACTGCTAGTAAA | 55833 |
rs769654000 | snp | A/G | 4.94376e-05 | 0.00497156 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923172 | TTATCCTGGAAAGGA[A/G]AGGTAAACACTACCT | 55833 |
rs769674199 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019840 | AAACAATTCCACTCT[C/T]ACGAAGCTCCTAGAA | 55833 |
rs769695864 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942051 | GCGTGCGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 55833 |
rs769736550 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026469 | TTTATGTTAAAGAAG[-/C]CAAGTCTTCATCAAG | 55833 |
rs769746988 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962045 | GAAACCACTAATACA[A/C]TGGAAATTTGGAGGA | 55833 |
rs769749621 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018388 | TACAAAAACTAGAAC[C/G]CTTGTGCACTGCTGA | 55833 |
rs769787073 | in-del | -/C | 1.6495e-05 | 0.0028718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924310 | CCAGGGAGGCTTGAT[-/C]AGCGACTGGCCCTGC | 55833 |
rs769794904 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032050 | CTTGGGAGGCTGAGG[C/T]GGGAGGATTGCTTGA | 55833 |
rs769797330 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | UBAP2 | GRCh38.p7 | 9:33923898 | TTCACGAAGGGCTGC[G/T]GGGCTGTGTGGTGGG | 55833 |
rs769800937 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946077 | AATCTCCTGGTTTAA[C/T]TGGTGGAAAATGGTA | 55833 |
rs769822864 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974017 | TCAAGACCAGCCTGG[A/G]CAACATAGGGAGACT | 55833 |
rs769882861 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971741 | AATCTGAATAGTCTG[C/T]AGGATTAAATGTCCT | 55833 |
rs769890649 | in-del | -/TACAAAATAATGTATG | 3.32585e-05 | 0.00407776 | intron-variant, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:34017159 | ATCATATACAGTATA[-/TACAAAATAATGTATG]TACAAAATAGAAAAT | 55833 |
rs769937768 | snp | G/T | 1.79599e-05 | 0.00299661 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922649 | GGAGCAGAACCCCTG[G/T]CCCAGAGTAGGGTGG | 55833 |
rs769971066 | snp | A/T | 1.65888e-05 | 0.00287996 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933660 | AGCTGTAAGAAGCAG[A/T]TCTGTTTATTTCTAA | 55833 |
rs769971349 | in-del | -/CTTTCTCG | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, frameshift-variant | UBAP2 | GRCh38.p7 | 9:33989035 | GTCCACGACTCGATT[-/CTTTCTCG]CTTTCTCGCTTTTCT | 55833 |
rs769992240 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947285 | TGCCCTAACCATAAA[C/T]CAGCCCACATGGCCA | 55833 |
rs770002383 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013652 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA | 55833 |
rs770004773 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997490 | CACAGCTCTCTGCAC[-/T]TATACCATTTGGCCT | 55833 |
rs770012989 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956177 | AAAAATTTAATCTTA[C/T]TCTACATACTACTAA | 55833 |
rs770050428 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949211 | AAAATAAAATAATAA[A/G]AAGTGATGTCATAAG | 55833 |
rs770087284 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963002 | ATAAATAAAAATAAT[A/C]TAATAAAAATAAAAA | 55833 |
rs770087946 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033160 | TATTGAAGAAATATC[G/T]GCATTCCTGTTTGTT | 55833 |
rs770095087 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993587 | TGGAGGATGGCATAA[A/G]CCCGGGAGGTCGAGG | 55833 |
rs770115771 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33944616 | GGCTAAGAACTGGGG[A/G]TGGCTCAGGTTGAGA | 55833 |
rs770117159 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBAP2 | GRCh38.p7 | 9:34048831 | GGCAATTACCGCTGC[C/T]GCTCTCGGAGGACCC | 55833 |
rs770124150 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949529 | CCAACGTGGTGAAAC[A/C]CCGTCTCTACTAAAA | 55833 |
rs770167925 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938073 | TGTGATCTCGGCTCA[C/T]TGCAACCTCCGCTTC | 55833 |
rs770183760 | snp | C/T | 1.65367e-05 | 0.00287543 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33988984 | TTACATTCTCTGCCA[C/T]GATTGCCGCCTCTTC | 55833 |
rs770202877 | snp | G/T | 1.64776e-05 | 0.00287028 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33956121 | GCTGGAGCAGATGAG[G/T]CAGTGAAGACCTTTG | 55833 |
rs770203994 | snp | A/G | 1.75557e-05 | 0.00296269 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948345 | AAACGTCCTCAGTAG[A/G]GGCAAACCCACAAAC | 55833 |
rs770210098 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950544 | GGACAGCTGTGACAG[A/G]GATTGCTCATACTGA | 55833 |
rs770210607 | snp | A/C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034028 | GGCATGACCCACCAC[A/C/G]CCCGGCTTCAAATCA | 55833 |
rs770215373 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988527 | TTGTCTATACCATGA[C/G]TGTCTATAAATGGAG | 55833 |
rs770220223 | snp | C/T | 3.30131e-05 | 0.00406269 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935761 | GACCAACTGGTGTTT[C/T]CCACATCACGTGAGC | 55833 |
rs770222439 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970416 | GCTAGGGTTGATGTT[A/G]TATGGATGTTTGTGT | 55833 |
rs770266024 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957502 | TTTAAATGAAATCAT[A/G]AAAGTATCCAAACCT | 55833 |
rs770268145 | snp | A/G | 3.34146e-05 | 0.00408732 | missense | UBAP2 | GRCh38.p7 | 9:33926990 | CGCCATACACTCACC[A/G]GGTAGGCAGGAAGCA | 55833 |
rs770286655 | snp | C/G | 3.29511e-05 | 0.00405887 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923482 | GGCTGGAGGGACCTG[C/G]GGGGGCAAGCAGATG | 55833 |
rs770289040 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955917 | TCAATTAGAAAATGA[C/T]TGAAGCTCTGTCAGA | 55833 |
rs770299427 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925133 | CACCATCCAGGGCCT[C/T]GCACTCCTGGACACA | 55833 |
rs770319674 | snp | C/T | 1.65124e-05 | 0.00287331 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953447 | ACTGTGAGGAACAGG[C/T]TTCTGGAGCAAGGCT | 55833 |
rs770326984 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | UBAP2 | GRCh38.p7 | 9:33923391 | CACCTGTACTGTAGC[C/T]GTGCTGGCCATAACC | 55833 |
rs770358277 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996527 | CTTTTCACTAACACT[A/G]GTAGAATCTAACTAC | 55833 |
rs770359318 | in-del | -/AAGG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938965 | GAAGGGGAAGAGAAA[-/AAGG]AAGGGAGGATGATCC | 55833 |
rs770399383 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018141 | GCCTAGACAACACTG[-/T]TAAGAACAACTCCAC | 55833 |
rs770414089 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000255 | ATGTAGCTTGGACTA[C/G]AGGTGCGCACCACCA | 55833 |
rs770421685 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989400 | TGGAGATGGGGTTTC[A/C]TCGTGTTAGCCATGA | 55833 |
rs770455738 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043962 | ACAAAATCCTGTCTC[C/T]ACAAAAAATACGAAA | 55833 |
rs770457869 | snp | A/G | 1.65214e-05 | 0.0028741 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922447 | CCCAAATACGTGCTC[A/G]TGTGTTCTCTCCTGC | 55833 |
rs770465364 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001102 | GATGAAGTAAAAGGG[A/T]AAAGCAAAGGGAGAG | 55833 |
rs770473072 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975432 | TGAGGCTCTATCTTT[-/A]AAAAAAAAAAAACAA | 55833 |
rs770489597 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010841 | TTATTATAAGAACAT[C/G]CCTGGTTTCAAGACA | 55833 |
rs770492256 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923503 | CAAGCAGATGAGGTA[G/T]TAGTGTAGGAAGAGG | 55833 |
rs770508150 | snp | C/T | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921281 | TCAGTTGATGACAAG[C/T]AAAAGACAGGTATAC | 55833 |
rs770533380 | in-del | -/GTG | 1.64741e-05 | 0.00286998 | cds-indel | UBAP2 | GRCh38.p7 | 9:33923946 | TGTGGCTGAGCTGGT[-/GTG]GTAGCGGGTGCAGGG | 55833 |
rs770546095 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977691 | TTTTTGAGACAGAGT[C/T]TTGCTCTGTCACCCA | 55833 |
rs770551181 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983195 | CCTATAATGTGTTTT[C/T]ATAACAATAAATCTG | 55833 |
rs770591093 | snp | A/G | 3.30371e-05 | 0.00406417 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973289 | CTTATGTCCTACACA[A/G]TTACACTTCCTTCTT | 55833 |
rs770591702 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945783 | CTCATTTTGGTGACT[A/G]CACAGAAATCTAGTA | 55833 |
rs770592116 | snp | C/T | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922348 | TACATAAATACATTA[C/T]ATACAGTAGCCAGTC | 55833 |
rs770610169 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017123 | CGAGCACCTCGACAA[C/T]GGTCACTGCTCACTG | 55833 |
rs770628580 | snp | A/T | 4.94262e-05 | 0.00497098 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33973221 | TCCTGCCCCTCTCCC[A/T]CTGCCACGTCCAAAT | 55833 |
rs770682283 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931510 | CAGCTCCACGGCACT[C/G]CTGCTGAGGTCAGCT | 55833 |
rs770688175 | snp | C/T | 3.32474e-05 | 0.00407708 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932520 | CTAAGCTCCAGGCTC[C/T]CCAAGCATGGCGGAG | 55833 |
rs770706963 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943695 | CCAGGCAATACTGGC[A/G]AGAAGAAGGAGTGAG | 55833 |
rs770715622 | in-del | -/TTCT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967039 | CCTCTATTTATTGTC[-/TTCT]TTATTTTCTCTCAAT | 55833 |
rs770724413 | in-del | -/CA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028152 | CGCTGACAGAAGAAT[-/CA]CAAAGTTATCTGCTG | 55833 |
rs770740928 | in-del | -/TATGTATGTATGTATGTATGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999887 | ATGTATGTATGTATG[-/TATGTATGTATGTATGTATGT]TATTTTGAGATGGAG | 55833 |
rs770758417 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946162 | TAAGTGTTCTTTACT[C/T]ATAGACTGTTCTTAT | 55833 |
rs770769929 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932278 | CGAGGAAAGATCAAA[C/G]AGCAAATTCCTGGGA | 55833 |
rs770794699 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | UBAP2 | GRCh38.p7 | 9:33924209 | GAGCAAACTCACCTG[A/G]ATATGGATTATTAGC | 55833 |
rs770829113 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038276 | AACACAGTGAAACTC[-/T]TGTCTCTATTAAAAA | 55833 |
rs770831879 | snp | C/G | 1.65836e-05 | 0.0028795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948607 | AAAAGGGGGATAAAA[C/G]AACAAATCCTCAACA | 55833 |
rs770844490 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026612 | AATCTAAAACCAATG[A/G]TAATGACAATACTAG | 55833 |
rs770885388 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018165 | ACTCCACCTCAATTT[-/A]AAAAAAAAAAAAAAT | 55833 |
rs770896014 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997391 | CAAAACAGCTTGATC[A/C]CAACATATCAAGTGA | 55833 |
rs770915568 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | UBAP2 | GRCh38.p7 | 9:33941657 | CACTTACCATGATGG[C/T]TCCTGGAGCTGACTC | 55833 |
rs770925842 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33954857 | TCATTTAGCATGAGA[C/T]TGATCCTGTTAGGTT | 55833 |
rs770933907 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941742 | ATAAGAGGAAGACAT[C/T]GCTACTGGACTAGCA | 55833 |
rs770942614 | snp | C/G | 4.97137e-05 | 0.00498542 | missense | UBAP2 | GRCh38.p7 | 9:33927839 | TACTGCTGCTGGATG[C/G]ACTCGCGGGGGTCCC | 55833 |
rs770951441 | snp | A/C | 3.29848e-05 | 0.00406095 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923148 | GGCAGGAGCCCACCA[A/C]TCCAGGCCTTATCCT | 55833 |
rs770961897 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047419 | AGTGGAATACATTCC[C/T]TTTCCTGAGGTAAAA | 55833 |
rs770977858 | snp | A/G | 2.5741e-05 | 0.00358746 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927130 | GTCACCACAAAGAGT[A/G]AGAGTCCTCAGCTGC | 55833 |
rs771017414 | snp | C/T | 1.66371e-05 | 0.00288414 | intron-variant | UBAP2 | GRCh38.p7 | 9:33996192 | AATTGGAGACAAATG[C/T]AAACAATGCAAATCA | 55833 |
rs771023787 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969566 | TAAAAAAAAAAAAAG[-/AAA]GAAAGAAAGAAAAGA | 55833 |
rs771034160 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985769 | GCTCATGCCTGTAAT[A/C]CTACCGCTTTGGGAG | 55833 |
rs771061747 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978844 | TAAATACAAAACAGT[A/G]AGGTAAAGCAGTGAG | 55833 |
rs771063165 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | UBAP2 | GRCh38.p7 | 9:33944493 | TCACAGTGGAGGGAC[G/T]GTCTCCAGGTGTTGA | 55833 |
rs771065466 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948097 | TACACAAAGTGTTAG[A/G]TGTTCATATTTGCAT | 55833 |
rs771069717 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | UBAP2 | GRCh38.p7 | 9:33923806 | TCACAAACATGGTGG[A/G]GCCATACTGGAAGGC | 55833 |
rs771100010 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923891 | TGCAGGATTCACGAA[A/G]GGCTGCTGGGCTGTG | 55833 |
rs771113358 | in-del | -/TTA | 1.65669e-05 | 0.00287805 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956174 | TTGAAAAATTTAATC[-/TTA]TTCTACATACTACTA | 55833 |
rs771129759 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950771 | GCACTATGTGCTTTA[A/C]AACACAGCGAAATCA | 55833 |
rs771131571 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925135 | CCATCCAGGGCCTCG[C/T]ACTCCTGGACACACC | 55833 |
rs771132132 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003699 | GGCGTGAGCCACCAC[A/T]CACGGCCAAAGAAAG | 55833 |
rs771161295 | snp | C/G | 1.65685e-05 | 0.00287819 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933524 | GGCTGCTAGTCAGGT[C/G]GCCAGTGTGCTGGGA | 55833 |
rs771199435 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025288 | TCCATCATCTATCAC[A/T]TTCCACTCCCAAGAG | 55833 |
rs771217476 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973620 | TAAGCTGAAGGCACT[A/G]TTAAGTATCATTTTA | 55833 |
rs771226263 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924936 | CTATCTTTAATGTTA[G/T]TGTATTTTATGTGTG | 55833 |
rs771239718 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032514 | CAGTCAGAAGGAAGG[A/T]AGATATCAAAATATA | 55833 |
rs771247734 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961892 | CTAGAAAAAGAGTCC[C/T]TATTTATGGAATGTT | 55833 |
rs771262808 | snp | A/G | 1.86041e-05 | 0.00304987 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963716 | AAATTAAAAAATTAA[A/G]TATTCATACCTTTGA | 55833 |
rs771282923 | snp | A/T | 1.65007e-05 | 0.00287229 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963822 | AAATTGAGGGTTTAA[A/T]CATATGAAAAGAATG | 55833 |
rs771340938 | snp | C/T | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050001 | TATCTTGTCACCCCA[C/T]AGATCGCCAGGGCTG | 55833 |
rs771343861 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000135 | TTTAATTTTTTAAAG[A/G]TAGGGTCTCATTCTG | 55833 |
rs771345097 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936678 | AACAAATAAATAAAT[A/T]AAGGAGACAATACCA | 55833 |
rs771357550 | snp | A/G | 1.71725e-05 | 0.00293018 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988938 | TCACTTGAGATGAAA[A/G]AAGAGAAAAAACTGA | 55833 |
rs771385180 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013516 | AAAACTCTCTTTCAT[A/C]ATGCAACCTGAATAG | 55833 |
rs771399940 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934411 | TTGACCCTTCTAAAA[C/G]CCAGGGAAAGCACTT | 55833 |
rs771405200 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995321 | AAGATCACACTACTG[A/C]ACTCCAGCCTGGGTG | 55833 |
rs771410505 | snp | A/G | 1.65545e-05 | 0.00287697 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935747 | ACGAATAAGCCATTG[A/G]CCAACTGGTGTTTTC | 55833 |
rs771411622 | snp | A/G | 1.77263e-05 | 0.00297705 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922636 | GGCTGTCAAGGCTGG[A/G]GCAGAACCCCTGGCC | 55833 |
rs771421539 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33933826 | TATCAAAGGACACCA[C/T]ACCATGGTCAGCTGT | 55833 |
rs771427881 | snp | A/G | 1.81358e-05 | 0.00301124 | missense | UBAP2 | GRCh38.p7 | 9:33922707 | CATCCTGCGGAAGGT[A/G]GTGGTGCAGCAGCTG | 55833 |
rs771449473 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022198 | TGCAGTGAGCTGAGA[C/T]TGCACCACTGCACTC | 55833 |
rs771453633 | in-del | -/C | 1.64728e-05 | 0.00286987 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33923384 | TACCCCTCACCTGTA[-/C]TGTAGCCGTGCTGGC | 55833 |
rs771482534 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006858 | TCAGACAATCAAAAC[A/G]ACTAGAGAAACTGAC | 55833 |
rs771487841 | snp | A/T | 6.58935e-05 | 0.00573955 | missense | UBAP2 | GRCh38.p7 | 9:33923830 | GGAAGGCACTGGGCA[A/T]GCCTGTGTAGTAGGG | 55833 |
rs771516677 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926685 | TGAGAACCAGAAAGT[A/G]TATTTTAGGAACCAC | 55833 |
rs771544535 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026432 | TGGGCTAAGGGTTCA[A/G]CTACTAAAAACAGGA | 55833 |
rs771591365 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045872 | CAAAATCTACCACAA[A/G]GATTACATGGTGATA | 55833 |
rs771600173 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963852 | GAAAGTATTCATCAC[A/C]GAGAAGATGGTCACT | 55833 |
rs771602474 | snp | A/T | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923380 | GAAGTACCCCTCACC[A/T]GTACTGTAGCCGTGC | 55833 |
rs771613626 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022907 | TCTGATCTTTTTCTC[A/C]CTGTTTATTCTCAGT | 55833 |
rs771628353 | in-del | -/AAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957100 | CCTCAAAAAAAAAAA[-/AAG]AAGAAGTCATTAAGA | 55833 |
rs771644504 | in-del | -/TTTTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989204 | ATGCATGTATCTTTC[-/TTTTTT]TTTTTTTTTTTGAGA | 55833 |
rs771668452 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987996 | TATGAAGGATATTGG[C/T]ATGGCTTGCTCCCCT | 55833 |
rs771705114 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046156 | AGATGTGCTTAAGGG[C/T]AGAGAACTTTACAAT | 55833 |
rs771753129 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936821 | AAAGAAACTGAAGCA[C/T]AGTGGCCCACACCTG | 55833 |
rs771757822 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975335 | TACCTGGGAGGCTGA[A/G]GCAGGAGAAATGCTG | 55833 |
rs771760254 | snp | C/G/T | 0.000155018 | 0.0088028 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922440 | CTGGGCTCCCAAATA[C/G/T]GTGCTCGTGTGTTCT | 55833 |
rs771766936 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008320 | CGAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 55833 |
rs771789965 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958177 | ATGTTGCCCAGGCTG[C/T]ACTTGATCTCTTGGG | 55833 |
rs771792596 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027941 | ACAAAGTCTACACCC[A/G]TAATCGAGGAGAGAA | 55833 |
rs771805382 | snp | A/T | 1.64743e-05 | 0.00287 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017102 | GCTGAAATCTGTGGT[A/T]TTTCCCGAGCACCTC | 55833 |
rs771830961 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943884 | CCAGCCTGGACAACA[C/T]GGCGAGACCCTGTCT | 55833 |
rs771852773 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938929 | GAAGGTAATTTTAAT[C/T]TGTGGATATTCCAGG | 55833 |
rs771860258 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946565 | GCCAGATAGTACAAC[A/C]ACCTAATATTTTAGC | 55833 |
rs771877483 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009249 | GATTACAGGTGCACA[A/C]CACCACGGCCAGCTA | 55833 |
rs771918320 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041740 | AAAGAAATCTACATG[G/T]GGGCTGGGTGCAGTG | 55833 |
rs771937806 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964775 | AAAAGCACTATAATA[C/T]CACATACAGATTTTT | 55833 |
rs771966667 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006089 | TACAAAAAAATTAGC[C/T]GGGCATGGTGGCGTG | 55833 |
rs772001176 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948477 | TGTACTTGGGGTGGT[A/G]GTAAACTGGCCCAAA | 55833 |
rs772012560 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983125 | CCTCGTGATCTGCTC[C/G]CCTCGGCCTCCAAAA | 55833 |
rs772012886 | in-del | -/GAGTTTGAGACCACCCT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960568 | ATCACCTGAGGTCAG[-/GAGTTTGAGACCACCCT]GACCAAAATGGTGAA | 55833 |
rs772030357 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008834 | GCTGAGCACAGTGGT[A/G]TGCGCCTGTAGTCCC | 55833 |
rs772046222 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048558 | GGGAGGCACCCCTGG[A/G]GCTGGGTGGGGCCCA | 55833 |
rs772052763 | in-del | -/TAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040576 | CATAGCGATACACTC[-/TAAT]TAATTAAAAAGAAGT | 55833 |
rs772055131 | in-del | -/AT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949191 | TAAATAAATAAATAA[-/AT]AAATAAAATAAAATA | 55833 |
rs772075366 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044683 | CCAATATGGCCAACA[C/T]GGTGAAATCCCATCT | 55833 |
rs772087752 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924197 | TCCTCATCCATTGAG[C/T]AAACTCACCTGGATA | 55833 |
rs772090679 | snp | C/T | 1.6525e-05 | 0.00287441 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948591 | AAGGACGGATGACTT[C/T]AAAAGGGGGATAAAA | 55833 |
rs772096627 | in-del | -/A | 1.71796e-05 | 0.00293079 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988935 | GGGTCACTTGAGATG[-/A]AAGAAGAGAAAAAAC | 55833 |
rs772112514 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33952239 | TCTAACTTCCCCTTG[A/C]CAGCTCAGAACTTCC | 55833 |
rs772147285 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002534 | AGGTGCATGCCACCA[C/T]GCCTGGCTAATTTTT | 55833 |
rs772149406 | snp | G/T | 1.64806e-05 | 0.00287054 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935886 | TGTCCATTCTATAAG[G/T]AAAAGAAGAGAAGAG | 55833 |
rs772149985 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003588 | TTTTTACTATTTTTA[C/G]TACAGATGCGGTTTC | 55833 |
rs772157514 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960243 | CCTAACACCTCAACC[A/T]TTTTTCTTGTTTGTT | 55833 |
rs772172115 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996402 | ATTAAGATTCTTCTA[C/T]ACAAATACAGAATTA | 55833 |
rs772179420 | snp | A/T | 3.56786e-05 | 0.00422351 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989175 | TTCAAAGTGTGTACA[A/T]TTATCAAAGGCACAT | 55833 |
rs772201540 | snp | C/G | 1.64833e-05 | 0.00287078 | missense | UBAP2 | GRCh38.p7 | 9:33960840 | CATCTTCAGTCCAGT[C/G]TTCTGTTGTCCACTC | 55833 |
rs772208658 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989443 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 55833 |
rs772240493 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959606 | TTATTATTTAACTTA[C/T]TTTTCCAAAAAAAAT | 55833 |
rs772248400 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941917 | TTAAATAGCTTCATA[-/A]AAAAAAAAAAACATA | 55833 |
rs772250986 | snp | C/T | 5.696e-05 | 0.00533636 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927086 | GGTGCTTTGCCTGTA[C/T]AGAGGGAAAAATCAA | 55833 |
rs772253764 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017483 | TACATGAAGTGCTAT[C/T]TGCCTCTTACTACTT | 55833 |
rs772271164 | snp | A/G | 1.72543e-05 | 0.00293715 | missense | UBAP2 | GRCh38.p7 | 9:33922592 | TGGCTGCGCTGACCC[A/G]AGCCACTCTGAGGAA | 55833 |
rs772347356 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929898 | AATCCCAGCTACTAG[C/G]GAGGCTGAGGCAGGA | 55833 |
rs772351822 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983758 | CTTTCTATCTTTGAC[A/C]ATAGTAAGTTTGAAA | 55833 |
rs772355727 | snp | C/T | 1.64768e-05 | 0.00287021 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996305 | GCCACTATGCATTCA[C/T]CCTGATTTTTCCCTG | 55833 |
rs772359316 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950873 | AATCAATGGAGAGAC[G/T]TTTAAAATGTATACA | 55833 |
rs772388646 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944401 | CCGCTTAGCAAGTTT[G/T]ATGTGTTTGGGCTGT | 55833 |
rs772400568 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014511 | GCAGGCACCTGTAAT[C/T]CCAGCTACTTGAGAG | 55833 |
rs772426217 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024091 | AGGATGGGCGCGGTG[A/G]CACACGCCTGTAATC | 55833 |
rs772433207 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025242 | CAAGTACCCAGTTGC[C/T]AGACCATAGGAATTC | 55833 |
rs772441643 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960910 | GCAATCAAAGTTTAT[A/G]CCACAAAGTCAAATA | 55833 |
rs772462393 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977649 | TCTACTACATCTCTG[C/T]TGAATGATTGTTCAA | 55833 |
rs772486070 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012672 | TAAGTGAAGAAGAAC[C/G]TTATTCACAACTACT | 55833 |
rs772509882 | snp | C/G | 1.64792e-05 | 0.00287042 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923792 | ACCCTCTGAAATACT[C/G]ACAAACATGGTGGGG | 55833 |
rs772518477 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33923631 | GCTGGATCTAAACAC[A/C]GCAGGGGAAAAGTGA | 55833 |
rs772538524 | in-del | -/GG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032891 | ACTGTACTCTGGCCT[-/GG]GCAACAGAGCAAGAC | 55833 |
rs772547545 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947740 | TGAGGTGGGAGGATG[A/G]ACTGAGCCTGGGAGG | 55833 |
rs772547548 | snp | C/G/T | 9.88426e-05 | 0.00702941 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944479 | CTGCAAAAGCTTGTT[C/G/T]ACAGTGGAGGGACTG | 55833 |
rs772549377 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047823 | TATCTCTAAAATTAA[C/T]AGTAATTTTTTAAAA | 55833 |
rs772558618 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979966 | TAGTCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 55833 |
rs772597799 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967968 | TTCTTTACTGCTGCT[C/G]TTCATTCTTTTCCAC | 55833 |
rs772623368 | snp | A/G | 3.31686e-05 | 0.00407225 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933516 | AGAGAGAGGGCTGCT[A/G]GTCAGGTCGCCAGTG | 55833 |
rs772650454 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008838 | AGCACAGTGGTGTGC[A/G]CCTGTAGTCCCAACT | 55833 |
rs772660248 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | UBAP2 | GRCh38.p7 | 9:33923384 | TACCCCTCACCTGTA[C/T]TGTAGCCGTGCTGGC | 55833 |
rs772670793 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010124 | AGGTCCTGTCTATTA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs772677061 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930527 | CACTTGTGGGGATAC[A/G]CAAGTGGGGAAAAAA | 55833 |
rs772697227 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020076 | GAAGCAGGATAATTG[C/T]TTGAACCTGGGAGGC | 55833 |
rs772703776 | snp | A/G | 2.50016e-05 | 0.00353556 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017009 | TATAATAATAAAAGA[A/G]AAAAAAGGAAAAAAA | 55833 |
rs772709396 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964878 | TTTCCCACCAGGCAT[C/G]TATATGAGTACCTGT | 55833 |
rs772736243 | in-del | -/TG | 1.64779e-05 | 0.00287031 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33922967 | CCTTTGTCCCTCACC[-/TG]TGTCTTATTGTAGAC | 55833 |
rs772741182 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954178 | TCCCAAAGTGCTGGA[A/T]TTACAGGCGTGAGCC | 55833 |
rs772745404 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34043135 | ACAATGACAACTCTA[A/C]ATGTTTTTATGCCTC | 55833 |
rs772750577 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005827 | TAAGAAAAATGTCTG[A/G]AAAACAAACCAAAAA | 55833 |
rs772798721 | in-del | -/TTAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999889 | TATGTATGTATGTAT[-/TTAT]GTATGTATGTATGTA | 55833 |
rs772811157 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033017 | AGAAAAACCATGACA[A/G]TACTCAACACACAGT | 55833 |
rs772892486 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981339 | TACAAATAAATAAAA[C/G]ACGGGGAAAGATACG | 55833 |
rs772910916 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994048 | TGCAGGCGCCCACCA[C/T]CACACCTGGCTAATT | 55833 |
rs772925145 | snp | A/G | 1.67256e-05 | 0.0028918 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943402 | TTTTGCTTCATAACA[A/G]AGGACTAAATTCAGT | 55833 |
rs772931596 | snp | C/T | 1.64863e-05 | 0.00287104 | missense | UBAP2 | GRCh38.p7 | 9:33943535 | GAGCCCCAAACTGCA[C/T]ATTTAATCCTGTGAC | 55833 |
rs772961730 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960003 | GGGCGGTCGAATGAT[-/A]AATGCAGCCTTGAAC | 55833 |
rs772967298 | in-del | -/TAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978409 | TAGAATGTTAAAACA[-/TAG]TAGGTGCTCAAAATT | 55833 |
rs772969814 | snp | A/T | 1.65855e-05 | 0.00287967 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971768 | TCCTGGGGTTTGAAA[A/T]AAAGAAATAATAAAG | 55833 |
rs772972804 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044691 | GCCAACATGGTGAAA[A/T]CCCATCTCTACTAAA | 55833 |
rs772974095 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015249 | CTTAGCACTTATCTC[A/G]CTTCACTTAAAATAA | 55833 |
rs772998914 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004203 | AACCTTTCCCAAAAC[A/G]GGCATAATGAACTTT | 55833 |
rs773003975 | in-del | -/TTAT/TTATTTATTTAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028393 | TATTTATTTATTTAT[-/TTAT/TTATTTATTTAC]TTTGAGATGGAGTTT | 55833 |
rs773007659 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952488 | AATCATTTGGCATTT[C/T]AAGAAAATGTAGCTT | 55833 |
rs773025266 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931444 | GAGTGCAGCTCCCCA[A/T]GAGTGCAGGAGCACT | 55833 |
rs773028043 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027968 | AGAACAAGGTATCTA[C/G]GGTGCCAAGAAACTC | 55833 |
rs773028981 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001370 | AAAGAAATGTGACCT[A/G]TTGTTTTGAAAGAAA | 55833 |
rs773029809 | snp | A/G | 2.08518e-05 | 0.00322885 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928037 | TCTGGAGGCAGAGGA[A/G]GAGGGTGCTGGGGAG | 55833 |
rs773044654 | snp | A/C | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935890 | CATTCTATAAGGAAA[A/C]GAAGAGAAGAGAATA | 55833 |
rs773045005 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029212 | ATGCACCCAAGAGAA[A/C]TGAAAACACGTTCAC | 55833 |
rs773057963 | snp | G/T | 1.65266e-05 | 0.00287455 | missense | UBAP2 | GRCh38.p7 | 9:33948406 | GAGGACTGGGATGTT[G/T]GGGGCTTGAGGTCCC | 55833 |
rs773076228 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | UBAP2 | GRCh38.p7 | 9:33948484 | GGGGTGGTGGTAAAC[C/T]GGCCCAAACTCGGAG | 55833 |
rs773080925 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983167 | ACAGATGTGAGCCAC[A/G]GTGCCCGGCCCCCCT | 55833 |
rs773084855 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001833 | AAGCACCACTGATGC[C/T]CATCCCTTCCCATCA | 55833 |
rs773103646 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989444 | CTGACCTCGTGATCT[C/G]CCCGCCTTGGCCTCC | 55833 |
rs773112478 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940799 | AAAAAACAAACAATC[C/T]ACAGAATTGCTCACA | 55833 |
rs773124208 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960342 | TCTGAAAATCTAAGT[G/T]CCTTTTAAGAAGCAT | 55833 |
rs773134866 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935791 | CTATCCTCTTCCTCT[A/G]TTTGGTTGGCACCAG | 55833 |
rs773169456 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046691 | GGCTTCACTTCAGAC[C/G]ACTCCAAACCTTCAA | 55833 |
rs773189067 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008962 | CAGCGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs773192694 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964270 | GCCAATACCATTCTG[G/T]GAGGCCTCTGGAAAA | 55833 |
rs773194932 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926862 | TCAGTGGGGCAGAGA[C/T]GGGGGTGCTCAGGGA | 55833 |
rs773203754 | snp | A/G | 1.66515e-05 | 0.00288539 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927022 | TCCTCCGGGACCTAC[A/G]AGGTACTGGTTGTGC | 55833 |
rs773296477 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963067 | AATAATTAAACACAA[-/C]CTTTGGACTTGCATA | 55833 |
rs773310113 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996482 | ATGAGGACATGTTTA[C/G]TTATTTTTTTGTGGC | 55833 |
rs773310250 | in-del | -/GAGGAGGAGGAAGAGGAGGAAGAGAAGGAGGAAGAGGAGGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016249 | GAAGGGGAGGAAGAG[lengthTooLong]GGAGGAAGAGGAGGA | 55833 |
rs773316184 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024569 | AGATGAAACAGGTTT[C/T]GCACAACAATCACAG | 55833 |
rs773316425 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982253 | CGCTTCAACCCAAAT[C/T]CTTTGCAAAAATCCT | 55833 |
rs773327051 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025494 | TCACCTCAAAGTGAA[-/TT]TTAAAGATGTGATAG | 55833 |
rs773364140 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925094 | AGCTTCGTGGAGGAG[A/G]GGAGGTCTGACCTGA | 55833 |
rs773396169 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949429 | CAGGTCAGGCTGGGC[A/G]CAGTGGCTCACACCT | 55833 |
rs773400152 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036421 | CGTGCCCAGCCTTGA[C/T]ACTTGATTCTATAGG | 55833 |
rs773412537 | snp | C/T | 4.94271e-05 | 0.00497102 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989056 | TCGCTTTTCTTCTCT[C/T]TATTCTCTTTGTTTT | 55833 |
rs773413060 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047840 | GTAATTTTTTAAAAT[A/C]TCTCAACTGTTAGGA | 55833 |
rs773419156 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960927 | CACAAAGTCAAATAC[A/G]GTCTCAGTCCAAATG | 55833 |
rs773435837 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon, missense | UBAP2 | GRCh38.p7 | 9:33960846 | CAGTCCAGTCTTCTG[C/T]TGTCCACTCTTCCAC | 55833 |
rs773437048 | in-del | -/TCT | 1.72782e-05 | 0.00293918 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941617 | CAAATAAGACGGACA[-/TCT]TCTGAGAAAAAAACT | 55833 |
rs773440700 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002598 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 55833 |
rs773460539 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959626 | CCAAAAAAAATACTA[C/T]GCTGAAAGCAGAACT | 55833 |
rs773460591 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029194 | GCAATCCTACTCCTG[A/G]GTATGCACCCAAGAG | 55833 |
rs773472588 | snp | A/G | 1.95861e-05 | 0.00312933 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927091 | TTTGCCTGTATAGAG[A/G]GAAAAATCAAATGGA | 55833 |
rs773500930 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998873 | CTGTTGCCTGGAAAG[C/T]ACATACAATTGTTAA | 55833 |
rs773506086 | in-del | -/GC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047715 | GCTGAGCACCGTGGT[-/GC]ACACTGTAATCCCAG | 55833 |
rs773546463 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045607 | TCGAACTCCCGACCT[C/T]GTGACCCGCCCGCCT | 55833 |
rs773556030 | snp | C/G | 3.29576e-05 | 0.00405928 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986717 | AACTGCCTGCTTCTT[C/G]CCCCTAATTGAAAGC | 55833 |
rs773557547 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923502 | GCAAGCAGATGAGGT[A/G]TTAGTGTAGGAAGAG | 55833 |
rs773575839 | snp | C/T | 3.29533e-05 | 0.00405901 | missense | UBAP2 | GRCh38.p7 | 9:33923800 | AAATACTCACAAACA[C/T]GGTGGGGCCATACTG | 55833 |
rs773576049 | snp | C/T | 3.01627e-05 | 0.00388336 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922480 | AGGATAAGCCTTGCC[C/T]CAGCCCACCCCTCTC | 55833 |
rs773580526 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018186 | AAAAAAAAATTATAA[C/G]CATAAGATTCCTACT | 55833 |
rs773623954 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997890 | TGAGACCTTTACTCC[A/G]AAGAACAATTATTAG | 55833 |
rs773628897 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947323 | AATGAATGAAATCCC[C/T]TGCTATTCCTTAATA | 55833 |
rs773633547 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992286 | CCAGCTACTCGGGAG[A/G]CTGAGGCGGAAGAAT | 55833 |
rs773651012 | snp | A/C/T | 3.31588e-05 | 0.00407167 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933519 | GAGAGGGCTGCTAGT[A/C/T]AGGTCGCCAGTGTGC | 55833 |
rs773661648 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967984 | TTCATTCTTTTCCAC[A/G]TTTCACAACAGTGGA | 55833 |
rs773702134 | in-del | -/AG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010865 | CAAGACATTTCAGAC[-/AG]AAACTACTTCATGCA | 55833 |
rs773716803 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955237 | ACCATTAAAAAAGTT[C/T]AGGCCAGGCGCGGTG | 55833 |
rs773716960 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971251 | CAACGTTGCTACAAA[C/T]CCATCTATCATCTAC | 55833 |
rs773736116 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978801 | AAGAAAGAAAGAAAG[A/T]AAAAGTAGAGGAACT | 55833 |
rs773781378 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011482 | TAGCATATTTATGAA[A/G]ATAAATTTTAATGAG | 55833 |
rs773794049 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974193 | AGACTCTGTCTCAAC[A/G]ACAACAACAAAATCT | 55833 |
rs773796286 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986172 | ATTCTCCTGCCTTAG[C/T]CTCTCAAGTAGCTGG | 55833 |
rs773811697 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019823 | AAACAAACTGTTTAT[C/G]CAAACAATTCCACTC | 55833 |
rs773815075 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024097 | GGCGCGGTGGCACAC[A/G]CCTGTAATCCCAGCA | 55833 |
rs773859149 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023219 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs773868291 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025249 | CCAGTTGCCAGACCA[C/T]AGGAATTCAGTGTAC | 55833 |
rs773874631 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | UBAP2 | GRCh38.p7 | 9:33923285 | TCCCCTGGGTCAGGT[C/T]GTCATAACCTAGCGT | 55833 |
rs773897114 | snp | C/T | 3.29777e-05 | 0.00406051 | missense | UBAP2 | GRCh38.p7 | 9:33927872 | CCAGACAGAGGCTGT[C/T]CGCGGTGTTCATGCT | 55833 |
rs773902306 | snp | C/G | 1.64904e-05 | 0.00287139 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926608 | CCGACCAGTCCATAC[C/G]CCACTCACCACTGGC | 55833 |
rs773916321 | in-del | -/TCCCGAGGCCAGGGGCCCAGTGGAGCCCAA | 1.80182e-05 | 0.00300146 | cds-indel | UBAP2 | GRCh38.p7 | 9:33922789 | ATAGCCAGGGGCCGC[lengthTooLong]GACCGAGGGCAGGCT | 55833 |
rs773977717 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962135 | ACACAGGGATATAAA[A/G]GAAAATTTCCAGGAG | 55833 |
rs773978735 | snp | C/T | 1.88248e-05 | 0.0030679 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953240 | GAATACATTTGCTAA[C/T]GGGTATATTTCTTAA | 55833 |
rs774049948 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017293 | ATAAAAGCTCTCTGG[-/A]ATACAAATTCTCAAG | 55833 |
rs774053977 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031966 | ACATAGCAAGACCTC[C/T]TCATCTCTACTAAAA | 55833 |
rs774120608 | snp | C/T | 3.3042e-05 | 0.00406447 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998845 | ATCACTTGAGCGAGA[C/T]GCATCTGTTCAGCTG | 55833 |
rs774122434 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026686 | GCACTTTATATGTAC[A/G]GTATTAAGTCACTAA | 55833 |
rs774136918 | snp | A/G | 4.99988e-05 | 0.00499969 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998912 | ACACCAAAAGCATAA[A/G]TTAGATTCCAAAATC | 55833 |
rs774157515 | snp | C/T | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922325 | CTTCTATCACATTTA[C/T]AAATACATACATAAA | 55833 |
rs774198679 | in-del | -/AGAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926310 | TTTTCTTTTTAAAAA[-/AGAG]AGAGAAAACAAGATG | 55833 |
rs774224323 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993657 | GGCAACGGAGTGAGA[C/T]CCTGTCTTAATAAAA | 55833 |
rs774225744 | in-del | -/TTTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002378 | CCACTGCATAGGTGC[-/TTTT]TTTTTTTTTTTTTTT | 55833 |
rs774227044 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971750 | AGTCTGCAGGATTAA[A/G]TGTCCTGGGGTTTGA | 55833 |
rs774264079 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982094 | CCCCACTCCTTGCAG[C/T]TGCTTTTTACAACTC | 55833 |
rs774267257 | snp | A/G | 1.66793e-05 | 0.0028878 | missense | UBAP2 | GRCh38.p7 | 9:33948388 | CCAAGATGACTGAGG[A/G]CTGAGGACTGGGATG | 55833 |
rs774271971 | snp | A/G | 1.80713e-05 | 0.00300588 | missense | UBAP2 | GRCh38.p7 | 9:33922763 | AAGATGTGTAGGAAT[A/G]GTGGGGGTGCATAGC | 55833 |
rs774277405 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033263 | GGTACTTATACACAA[C/T]AGAGTACTACTTAGC | 55833 |
rs774280015 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042393 | GGAGGCTGGAGATTC[A/G]CTTGAACTTGGGAGG | 55833 |
rs774286920 | in-del | -/AAATAC | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954723 | AATTCACTGAATCAT[-/AAATAC]AAATACAATAGAGAA | 55833 |
rs774295939 | snp | C/G/T | 3.30165e-05 | 0.00406293 | utr-variant-5-prime, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33988989 | TTCTCTGCCACGATT[C/G/T]CCGCCTCTTCCTTTC | 55833 |
rs774299051 | snp | A/T | 1.72463e-05 | 0.00293647 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944652 | AGTCTAAAAAAAGTA[A/T]GCAGCAATTAATGAG | 55833 |
rs774329490 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923990 | CCCACGGCCAAACTT[C/T]GTGACATCACCTAGG | 55833 |
rs774335932 | in-del | -/CTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026905 | TAGTTCCCAATTCAG[-/CTT]CTTCTTCTATACAAC | 55833 |
rs774346873 | in-del | -/TATGTATGT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999899 | ATGTATGTATGTATG[-/TATGTATGT]TATTTTGAGATGGAG | 55833 |
rs774361919 | snp | G/T | 1.79056e-05 | 0.00299207 | missense | UBAP2 | GRCh38.p7 | 9:33922831 | CAAGACCGAGGGCAG[G/T]CTGAAAGGTGGAGGC | 55833 |
rs774367918 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957710 | GATCTAATGAGGTAA[A/C]ACGGAAAACATAAAA | 55833 |
rs774426064 | in-del | -/AAAT | 3.52485e-05 | 0.00419798 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953268 | TAAAATCCCACACTG[-/AAAT]AAAAGTGAGTTACCA | 55833 |
rs774524981 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970677 | GCTCAAGTGATCCTC[C/T]CGCCTTGGCCACCTA | 55833 |
rs774542705 | snp | A/C/G | 1.64879e-05 | 0.00287118 | missense | UBAP2 | GRCh38.p7 | 9:33927874 | AGACAGAGGCTGTTC[A/C/G]CGGTGTTCATGCTAC | 55833 |
rs774564497 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024038 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAT | 55833 |
rs774572513 | snp | A/T | 3.29603e-05 | 0.00405944 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935882 | ACCATGTCCATTCTA[A/T]AAGGAAAAGAAGAGA | 55833 |
rs774623225 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010616 | AGGTAATAGAACATA[C/T]GGATATTGACTGTAC | 55833 |
rs774624331 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33988699 | CCAGGTCAATGCTGA[C/T]ACGAAACCACATGGG | 55833 |
rs774629895 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33933178 | TGACATGGGCCCAGC[A/G]ATGCCCAGAGAGGCT | 55833 |
rs774636664 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935774 | TTTCCACATCACGTG[A/G]GCTATCCTCTTCCTC | 55833 |
rs774648972 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938512 | CAAAAACAGCTTGTC[A/G]TTGGCCGGGCGTGGT | 55833 |
rs774655513 | in-del | -/ATG | 4.98848e-05 | 0.00499399 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998759 | AAATAGATTATAAAA[-/ATG]ATGATATCCTTTGCC | 55833 |
rs774664258 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923410 | CTGGCCATAACCACT[A/G]GCCTGCTGGAAGGGA | 55833 |
rs774694445 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34009485 | GGATGGTCTTGAACT[A/C]CAGAGCTCAAACAAT | 55833 |
rs774717410 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030652 | AAATAAGGGGCCAGG[C/T]ACGGTGGCTCACGCC | 55833 |
rs774737292 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011119 | ACAAGCACTTGATGG[G/T]TGAAAGAATCTCACC | 55833 |
rs774744907 | snp | A/G | 1.66482e-05 | 0.0028851 | missense | UBAP2 | GRCh38.p7 | 9:33927015 | GAAGCAGTCCTCCGG[A/G]ACCTACGAGGTACTG | 55833 |
rs774766176 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960813 | AAGGTCTCATCTGAC[A/G]GCAAACACTTACATC | 55833 |
rs774771747 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925139 | CCAGGGCCTCGCACT[C/T]CTGGACACACCTGGC | 55833 |
rs774782828 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949480 | AGCCGAGGTGGGTGG[A/G]TCACCTGAGGTCAGG | 55833 |
rs774783988 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050476 | TTTGTACAGGGCACT[A/G]TGCTAATTACTAATT | 55833 |
rs774786263 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | UBAP2 | GRCh38.p7 | 9:33944393 | GGTATCCGCCGCTTA[G/T]CAAGTTTGATGTGTT | 55833 |
rs774797819 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989969 | AAATTTTTAACCTCC[-/A]AAGAATTCTTCTAGT | 55833 |
rs774799997 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978151 | AACCTATCTGTTCAG[A/T]AACTGATTTGAGAAT | 55833 |
rs774821412 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021930 | TGAGCCACTGTGCCC[A/G]GCCCCATTGGATTAT | 55833 |
rs774837506 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33995326 | CACACTACTGCACTC[A/C]AGCCTGGGTGGCAGA | 55833 |
rs774883364 | in-del | -/TTC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950064 | AAAATAACATTTCTT[-/TTC]TTCTTTTCTTTTTTC | 55833 |
rs774884834 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034478 | AAACATTAACACACC[A/T]GCCACATAAGTATCT | 55833 |
rs774890459 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965089 | TTGCTTTTAATTAAC[-/TTT]TTATCTTAAAATAAT | 55833 |
rs774899812 | snp | A/G | 1.66643e-05 | 0.0028865 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933502 | TACCTGCTAAGCTGA[A/G]AGAGAGGGCTGCTAG | 55833 |
rs774902297 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923485 | TGGAGGGACCTGGGG[A/G]GGCAAGCAGATGAGG | 55833 |
rs774902521 | snp | A/G | | | downstream-variant-500B | UBAP2 | GRCh38.p7 | 9:33921554 | ATTTGGGCCAAGAGG[A/G]TCCAGTAAAAAGGAA | 55833 |
rs774942322 | snp | G/T | 1.7205e-05 | 0.00293295 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932635 | GAGAGCGAACTAGAA[G/T]ACAAAACAGAGCGCC | 55833 |
rs774944705 | snp | A/T | 1.66938e-05 | 0.00288905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948630 | CCTCAACAATACAGA[A/T]TTTCTGCCCAAGGCT | 55833 |
rs774948119 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941210 | ATCAAAAATAGATCT[A/G]GTTCCTTTATCTATA | 55833 |
rs774981430 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34020486 | CGCGCCACCATGCCC[A/G]GCTAATTTTTGGTAT | 55833 |
rs774985647 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953806 | TTGGTTCATTTTACC[C/T]AGAATATTTTACCCA | 55833 |
rs774987865 | snp | A/G | 8.24165e-05 | 0.00641883 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924290 | CATAGTAGTCCTAGG[A/G]GAGACCAGGGAGGCT | 55833 |
rs774993785 | in-del | -/CATT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932931 | CATCCTTGACAATCC[-/CATT]CAATCTGTGAACGAG | 55833 |
rs774999663 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984048 | AGCTGGAACTACAGG[A/C]ACACACCACCATGCC | 55833 |
rs775003963 | snp | G/T | 1.94657e-05 | 0.00311969 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922503 | CCCCTCTCTTCTGGG[G/T]TTAGTTTGTCCAGTA | 55833 |
rs775027881 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955043 | GTGGTTATCCCATAA[C/G]TTCCTTCCTTTTCTG | 55833 |
rs775095920 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983401 | TAATGCCAGCAGAAG[C/T]ATGTGAGAGATCAAA | 55833 |
rs775101887 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33924231 | ATTATTAGCTAGGCT[C/T]CCATCTCGGCTGGCA | 55833 |
rs775114778 | snp | A/C | 3.29571e-05 | 0.00405924 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33973231 | CTCCCTCTGCCACGT[A/C]CAAATCCTTTAAAAA | 55833 |
rs775131143 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030579 | AGTATGCCGTGATCA[C/T]GCCAGTGCACTCCTA | 55833 |
rs775146242 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997698 | CCAGTGATCAGATTA[C/T]TGACAGACAGAACTA | 55833 |
rs775185674 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967900 | AACTTGTCTCTTTGA[A/T]ACCAAGAAGAAATTT | 55833 |
rs775216086 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047591 | TGAAAAAAGTGCTGT[C/G]ACAACGGAAGAGGAA | 55833 |
rs775244482 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040745 | CCACTCAGTCTTTGA[C/G]AATGAATTCCCAATT | 55833 |
rs775255618 | in-del | -/TGGCCCTGCT | 1.65151e-05 | 0.00287355 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924317 | GGCTTGATCAGCGAC[-/TGGCCCTGCT]TGACTCCCAGGAGAG | 55833 |
rs775268639 | snp | A/C/G | 3.29534e-05 | 0.00405904 | missense | UBAP2 | GRCh38.p7 | 9:33922994 | TAGACAGAACCAGTC[A/C/G]TATCAGGTAGACCAG | 55833 |
rs775277553 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013161 | TAGCTCAAAAAAAAA[-/AA]AAAAAAAAAAAAAGA | 55833 |
rs775283029 | snp | A/C | 1.64789e-05 | 0.0028704 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923173 | TATCCTGGAAAGGAG[A/C]GGTAAACACTACCTT | 55833 |
rs775291110 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029623 | GGAGGACCACTTGGG[C/T]TCAGGAGTTCGAGAC | 55833 |
rs775302756 | in-del | -/CTGCTT | 0.000158667 | 0.00890553 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935722 | AAAAAAGCAAAAGGG[-/CTGCTT]TTTAACGAATAAGCC | 55833 |
rs775307912 | snp | C/G | 7.23759e-05 | 0.00601521 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927765 | CTTTGAGGGGCTCAG[C/G]GGTGGGCAGGAAAGG | 55833 |
rs775313157 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003821 | ACTTCCCAGGTTGAA[A/G]CAATTCTAGTGTCTC | 55833 |
rs775328875 | snp | A/T | 1.65007e-05 | 0.00287229 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953341 | CAGTCCCTGGTGCCA[A/T]CTGATTGTTGTGTTG | 55833 |
rs775379153 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962068 | TTGGAGGATGAAGTT[A/G]ATGAAAGCCAGAATT | 55833 |
rs775398961 | snp | A/G | 1.65078e-05 | 0.00287291 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963838 | CATATGAAAAGAATG[A/G]AAGTATTCATCACAG | 55833 |
rs775401357 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049048 | CTCCACCCCAACCCC[A/G]CGAAGCCAACCGCGT | 55833 |
rs775402382 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030352 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 55833 |
rs775418992 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33941772 | AGAATTCAGTGATGA[C/G]CTTGTCAGACTGCAG | 55833 |
rs775426764 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930110 | TGTACAACCTCATTA[A/G]AAACTAGACTGATGG | 55833 |
rs775427916 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013663 | GGGCGGATCACCTGA[C/G]GTCAGAAGTTTGAAA | 55833 |
rs775445720 | snp | A/G | 1.65004e-05 | 0.00287227 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33963752 | TAAGAACTTTTGTTT[A/G]ACAGATCCTGAGCTA | 55833 |
rs775466476 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968038 | TTGACAGGAACAAAT[C/T]CAGTATCCATTGATT | 55833 |
rs775473813 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037999 | AACCCTGTCTCTACA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs775477008 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925189 | CCTTGGGCTGTGCCC[A/G]ATCCCAGAAAGGAGC | 55833 |
rs775480917 | snp | C/T | 5.39719e-05 | 0.00519452 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922652 | GCAGAACCCCTGGCC[C/T]AGAGTAGGGTGGCTG | 55833 |
rs775487846 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048645 | AAGGAGGGAGCCCGG[A/G]CCTGGACGTAGAGGG | 55833 |
rs775493912 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969472 | TGGGATGGCTTGAAC[C/G]CAATGGTTCAAGGCT | 55833 |
rs775496234 | in-del | -/T | 6.61529e-05 | 0.00575083 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924325 | AGCGACTGGCCCTGC[-/T]TTGACTCCCAGGAGA | 55833 |
rs775503473 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956691 | AATCAGGAAAATGAT[C/G]AGACTAATGGTAAAC | 55833 |
rs775540827 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960963 | TTTTTGTGTACTATG[C/T]GGGGAAAAAAGATAC | 55833 |
rs775549504 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941209 | TATCAAAAATAGATC[G/T]GGTTCCTTTATCTAT | 55833 |
rs775566631 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045909 | CATGTCCTCCCTCTC[-/T]TTTGCCTTCCTTCAG | 55833 |
rs775591991 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019858 | GAAGCTCCTAGAACA[A/G]ACAAAACAAAAACAA | 55833 |
rs775594520 | snp | A/G | 4.94246e-05 | 0.0049709 | missense | UBAP2 | GRCh38.p7 | 9:33923980 | ATGCAGAGTCCCCAC[A/G]GCCAAACTTTGTGAC | 55833 |
rs775605599 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33936129 | CTGGGACTACAGGTG[A/C]ATCCTACCATGCCTA | 55833 |
rs775611584 | snp | C/T | 8.2373e-05 | 0.00641714 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989042 | GACTCGATTCTTTCT[C/T]GCTTTTCTTCTCTCT | 55833 |
rs775616810 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970525 | TCCTCAACCTGCCAG[A/G]CTCAAGTGACACTCC | 55833 |
rs775640025 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967340 | TTATTGCACTGGCTA[A/G]GACCTCCAGTACAGT | 55833 |
rs775677780 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | UBAP2 | GRCh38.p7 | 9:33944501 | GAGGGACTGTCTCCA[C/G]GTGTTGATTCTCGAA | 55833 |
rs775687507 | in-del | -/AGAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945659 | ACAATATATATAGAC[-/AGAC]AGACAGACAGACAGA | 55833 |
rs775719624 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934671 | AAGCCTCTCTCAAAC[A/T]AACAAACAAAATGGG | 55833 |
rs775754889 | snp | C/G | 1.6546e-05 | 0.00287624 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926709 | GAACCACATACCACA[C/G]CCTGGGAAGCCCAGG | 55833 |
rs775760736 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34007322 | GGTAACTTGGTGAGA[C/T]GCTGTCTCTTCAAAA | 55833 |
rs775763400 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000262 | TTGGACTACAGGTGC[A/G]CACCACCACATCTGG | 55833 |
rs775774831 | snp | A/G | 1.81155e-05 | 0.00300955 | missense | UBAP2 | GRCh38.p7 | 9:33922730 | AGCAGCTGTGAGTGG[A/G]GCTGCTGGTGGGCTG | 55833 |
rs775776310 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042498 | AAAAAAAAAAAAAAG[A/G]AACAGTAGAACCTGC | 55833 |
rs775780791 | in-del | -/TCTAT | 1.64757e-05 | 0.00287012 | utr-variant-5-prime, frameshift-variant | UBAP2 | GRCh38.p7 | 9:33989055 | CTCGCTTTTCTTCTC[-/TCTAT]TCTCTTTGTTTTCTG | 55833 |
rs775783356 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976905 | TAATGCCAGCTATTA[C/G]GGAGGCTGAGGCAGG | 55833 |
rs775783977 | snp | A/G | 1.71557e-05 | 0.00292875 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948366 | ACCCACAAACAATGT[A/G]TACCTACCAAGATGA | 55833 |
rs775809130 | snp | C/G/T | 3.30443e-05 | 0.00406464 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33988985 | TACATTCTCTGCCAC[C/G/T]ATTGCCGCCTCTTCC | 55833 |
rs775815733 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33926637 | GCAGCCGTGACTGCA[A/G]CATCTGGAGCTCGTC | 55833 |
rs775823124 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021880 | CTCGGGTGATCCAAC[C/T]GCCTCAACCTCCCAA | 55833 |
rs775839079 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014516 | CACCTGTAATCCCAG[C/G]TACTTGAGAGGCTGA | 55833 |
rs775849094 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003376 | TACATCAAAGATGGC[-/TTT]TTTTTTTTTTTTTGA | 55833 |
rs775873793 | snp | A/C/T | 3.2998e-05 | 0.00406179 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935765 | AACTGGTGTTTTCCA[A/C/T]ATCACGTGAGCTATC | 55833 |
rs775881200 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950877 | AATGGAGAGACTTTT[A/G]AAATGTATACAATAC | 55833 |
rs775898792 | snp | G/T | 1.65277e-05 | 0.00287464 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953455 | GAACAGGCTTCTGGA[G/T]CAAGGCTACCAGATC | 55833 |
rs775900421 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010123 | GAGGTCCTGTCTATT[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs775913404 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33956123 | TGGAGCAGATGAGGC[A/G]GTGAAGACCTTTGTT | 55833 |
rs775940049 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928098 | AAGGCTGAGCAGGCA[A/G]GCAATGATGTAACCA | 55833 |
rs775943163 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34034816 | AGGCGGAGGTTGCAG[C/T]GAGTCAAGATCACGC | 55833 |
rs775946305 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33956320 | CAAGTGAATGCAATT[-/T]TTTTTTTTTTTTTTT | 55833 |
rs775957129 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003761 | GTTTCACTCTTGTTG[C/T]CCAGGCTGGAGTGCA | 55833 |
rs775961172 | in-del | -/AAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942384 | TTAAAAAGGAAACTT[-/AAAC]AAATATCAGGTTTTG | 55833 |
rs776047582 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966294 | CTCTACTAAAACTAC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs776061375 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997551 | AGCAAAAGTTCTGCA[A/T]ACTCTATAGCTTTCT | 55833 |
rs776067164 | snp | A/C/G/T | 0.000263588 | 0.0114775 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923483 | GCTGGAGGGACCTGG[A/C/G/T]GGGGCAAGCAGATGA | 55833 |
rs776069209 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033220 | GAAGTAACCTAAGTG[A/T]CTATCAACAGGTGAA | 55833 |
rs776074777 | snp | C/T | | | intron-variant, downstream-variant-500B | UBAP2, SNORD121A | GRCh38.p7 | 9:33952684 | ACACAAGGAAAACAT[C/T]ATTCAGAAGAAAGGG | 55833 |
rs776092880 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010429 | AAACTCTGCCTCATA[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs776093485 | snp | C/G | 1.6516e-05 | 0.00287362 | missense | UBAP2 | GRCh38.p7 | 9:33943562 | TGACATCTGCTGAAC[C/G]AGGCATTTCCACTGC | 55833 |
rs776125987 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953691 | TGCAGAGAAGAGAAT[A/C]AAAAGGTGTATTGAG | 55833 |
rs776138455 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996603 | GCAGCACACACATAC[A/G]TACCAACATTCTCAG | 55833 |
rs776160870 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976410 | GAACCCAAAACATTA[G/T]CTAAGAGAAAGAAGC | 55833 |
rs776161092 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966569 | GACATTTCAAAGATA[C/T]TGAGTCTTCTAATTC | 55833 |
rs776182355 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028209 | AAAGGATGAGTGCTG[A/G]TGAACTCAAACACTA | 55833 |
rs776187739 | snp | A/C | 1.6912e-05 | 0.00290787 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017032 | GAAAAAAAAAAAAAG[A/C]GTTCCACAAAAACTT | 55833 |
rs776247072 | snp | C/T | 0.000149545 | 0.00864582 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932531 | GCTCCCCAAGCATGG[C/T]GGAGGAAGAGGAAGC | 55833 |
rs776261315 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983256 | CCTTAAACATGTCTC[G/T]AAACAACCAATCCAA | 55833 |
rs776281259 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017124 | GAGCACCTCGACAAT[A/G]GTCACTGCTCACTGA | 55833 |
rs776364510 | in-del | -/TGTTCCCCACAGCAG | 1.64901e-05 | 0.00287137 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923051 | AGGAGGAAAAGCAGT[-/TGTTCCCCACAGCAG]TTGTTCCCAGCTCCA | 55833 |
rs776385705 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947981 | GGAAGACCCCATCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs776387479 | snp | A/G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001530 | TTACAGCATGTCATT[A/G/T]TGGCAGCTGGCCTGC | 55833 |
rs776402001 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983977 | AGTGCAATGGTACAA[C/T]CTCGGCTCACTGCAG | 55833 |
rs776409928 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002705 | TAAGCTAGGGTTTCA[C/T]TGTGTCGGCTAGGCT | 55833 |
rs776410886 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924165 | CTGGAGTTCGCGCTA[C/G]GCCGGCCCCGGGCTA | 55833 |
rs776413517 | in-del | -/GAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940435 | CAGAGTTGTTGAGCT[-/GAA]ATCCTAAGCTATCAT | 55833 |
rs776419951 | in-del | -/GGCTTGAATGGGGAGGGCAGA | 1.64833e-05 | 0.00287078 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924037 | GCCACTGCCCTTCCT[-/GGCTTGAATGGGGAGGGCAGA]CCAACCAGAGAAAGG | 55833 |
rs776429442 | snp | A/C/G | 0.0002622 | 0.0114472 | missense | UBAP2 | GRCh38.p7 | 9:33922874 | AATCCCTGCTTGTCA[A/C/G]AAGTCTACAGGGCAA | 55833 |
rs776429535 | snp | A/C | 1.64743e-05 | 0.00287 | missense | UBAP2 | GRCh38.p7 | 9:33924212 | CAAACTCACCTGGAT[A/C]TGGATTATTAGCTAG | 55833 |
rs776454992 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989588 | ATAGTTCTACTTTAT[C/T]GATGATGAAGGTAAC | 55833 |
rs776460172 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032970 | ATACTCTAAGCCACA[A/G]TGTTTAACTCTTGCT | 55833 |
rs776461571 | snp | A/G | 6.59674e-05 | 0.00574277 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927903 | ACTGGACAGGCTGGC[A/G]CCTGAGGATGCGGAA | 55833 |
rs776477558 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935907 | AAGAGAAGAGAATAT[A/G]AACTTACAAAATGAA | 55833 |
rs776485514 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017981 | TGTTGAACAAACATT[C/T]ATTGACTAGCTACTA | 55833 |
rs776496603 | snp | G/T | 1.64895e-05 | 0.00287132 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33941661 | TACCATGATGGTTCC[G/T]GGAGCTGACTCTGAT | 55833 |
rs776512887 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978862 | GTAAAGCAGTGAGAA[A/C]GGTTAGGGAGTAAAC | 55833 |
rs776535019 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929123 | GCCTGCCCACCAACT[A/G]GGTTCTCACTAAGGA | 55833 |
rs776538494 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949468 | AGCACTTTGGGAAGC[C/T]GAGGTGGGTGGATCA | 55833 |
rs776542222 | in-del | -/CA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024342 | AGCAAAACTCTGTCT[-/CA]AAAAAAAAAAAAATA | 55833 |
rs776545065 | snp | G/T | 1.66142e-05 | 0.00288216 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948614 | GGATAAAAGAACAAA[G/T]CCTCAACAATACAGA | 55833 |
rs776548440 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983653 | CTTTTTGTTACCTTC[C/T]ATTTTCTTTTTCTTC | 55833 |
rs776579031 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941943 | ACATAAACAGCTTCA[C/T]GAGATGCAACTACTG | 55833 |
rs776585087 | snp | A/T | 2.64911e-05 | 0.00363935 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927131 | TCACCACAAAGAGTG[A/T]GAGTCCTCAGCTGCT | 55833 |
rs776599471 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985522 | CCTTTGGAGCAACAT[C/G]AATGGACTTGGAAGA | 55833 |
rs776628749 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33934465 | CAAAAACAAACATAA[A/G]CAATGAAAGGGTCAA | 55833 |
rs776707024 | in-del | -/AAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010428 | GAAACTCTGCCTCAT[-/AAAA]AAAAAAAAAAAAAAA | 55833 |
rs776741467 | in-del | -/TGAACCCGGTGGGCAGAGGTTGCAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044784 | GGCAGGAGCATCACT[-/TGAACCCGGTGGGCAGAGGTTGCAG]TGGGCGAAGATCGTA | 55833 |
rs776742746 | snp | C/T | 4.96463e-05 | 0.00498203 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927843 | GCTGCTGGATGCACT[C/T]GCGGGGGTCCCACCC | 55833 |
rs776747292 | snp | C/G | 4.95757e-05 | 0.00497849 | missense | UBAP2 | GRCh38.p7 | 9:33944593 | GTGCTGTTGTCGCTG[C/G]CTCAACTGGCTAAGA | 55833 |
rs776757033 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979654 | TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT | 55833 |
rs776763676 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968049 | AAATCCAGTATCCAT[C/T]GATTTCTTCTCAAAA | 55833 |
rs776798030 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000225 | GTTCAAGAGATCCTG[A/C]CGCCTCAGCCTCCCA | 55833 |
rs776827275 | snp | C/G | | | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996317 | TCATCCTGATTTTTC[C/G]CTGTCACTTCCATAA | 55833 |
rs776831459 | snp | G/T | 1.64798e-05 | 0.00287047 | missense | UBAP2 | GRCh38.p7 | 9:33960854 | TCTTCTGTTGTCCAC[G/T]CTTCCACAGAATTCT | 55833 |
rs776854774 | snp | A/T | 1.64751e-05 | 0.00287007 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944497 | AGTGGAGGGACTGTC[A/T]CCAGGTGTTGATTCT | 55833 |
rs776858373 | in-del | -/A | 0.000410727 | 0.0143246 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988944 | GAGATGAAAGAAGAG[-/A]AAAAACTGAGGAGAA | 55833 |
rs776859015 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33948115 | TTCATATTTGCATGC[A/T]TTTACCATACTTTTC | 55833 |
rs776865936 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991006 | ATAAAACAACGTGGC[C/T]GAGCACACTGGCTCA | 55833 |
rs776866077 | snp | C/T | 1.64792e-05 | 0.00287042 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986810 | TTGTCCACTTGATTG[C/T]AATCAATTCCATTTT | 55833 |
rs776870084 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33925772 | ACACCCACGGGGAAG[-/A]AAGGCATCACTGCAC | 55833 |
rs776871635 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34050575 | TTCATCTGAATTAAA[A/G]AATGCTGCCGGGCGT | 55833 |
rs776901095 | snp | A/G | 1.65353e-05 | 0.00287531 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933640 | GGAGCTGGAACAGAT[A/G]AAGTAGCTGTAAGAA | 55833 |
rs776909929 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33923894 | AGGATTCACGAAGGG[C/T]TGCTGGGCTGTGTGG | 55833 |
rs776915347 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33986699 | GTCACAGTCCAGCAA[C/T]GCAACTGCCTGCTTC | 55833 |
rs776946733 | snp | C/T | 8.24328e-05 | 0.00641947 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933594 | CAGGGAGCTCACAGA[C/T]GGGAGGGCAGAGGGA | 55833 |
rs776954339 | snp | C/T | 3.29843e-05 | 0.00406092 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953362 | TGTTGTGTTGCGAAT[C/T]TGTGAAGACAAGGGC | 55833 |
rs776957743 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032074 | TGCTTGATCCCAGGA[C/T]TTCGAGGCTACAGTG | 55833 |
rs776983902 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985401 | TTCACAATATTCACA[A/C]ATATAGAGAATCAAC | 55833 |
rs776989578 | snp | A/G | 1.73586e-05 | 0.00294601 | missense | UBAP2 | GRCh38.p7 | 9:33922574 | GGCTGCAGGGAGCTG[A/G]GCTGGCTGCGCTGAC | 55833 |
rs776995348 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34024204 | AAAATTAGCCGGGCG[A/T]GGGGGCACATGCCCA | 55833 |
rs776995878 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017958 | TGTGCATATAATTTT[A/C]TTTGATTTGTTGAAC | 55833 |
rs777010349 | in-del | -/A/AG | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922036 | AGTTTCTCAAAAACA[-/A/AG]GAGGTATGAAGTAAT | 55833 |
rs777021118 | snp | A/G | 1.65184e-05 | 0.00287384 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924318 | GCTTGATCAGCGACT[A/G]GCCCTGCTTGACTCC | 55833 |
rs777077241 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989364 | CTGCCACCACGCCCA[A/G]CTAATTTTTTGTATT | 55833 |
rs777093577 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979576 | AGAAATTCCCGTCTC[-/A]AAAAAATAAAAATAA | 55833 |
rs777110723 | snp | C/T | 1.64933e-05 | 0.00287165 | missense | UBAP2 | GRCh38.p7 | 9:33926627 | CTCACCACTGGCAGC[C/T]GTGACTGCAGCATCT | 55833 |
rs777143645 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046644 | ACAAGACTCCATCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 55833 |
rs777143730 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924974 | ACAATTATTCTTTCA[A/G]TGTGGCCCAAGGAAG | 55833 |
rs777145204 | snp | A/G | 1.67897e-05 | 0.00289733 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988965 | CTGAGGAGAAAGTCT[A/G]TACTTACATTCTCTG | 55833 |
rs777146249 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022944 | ATTTATGAAAATAAT[C/T]GGCTGGGTGCAGTGG | 55833 |
rs777169623 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33969059 | TATTCTATATTTTGC[G/T]TATACATTCATCCAT | 55833 |
rs777181143 | in-del | -/A | 3.46188e-05 | 0.00416032 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932638 | AGCGAACTAGAAGAC[-/A]AAACAGAGCGCCGTA | 55833 |
rs777195945 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944035 | CTGACTACTCTATTT[C/T]TGGGGACTCACCAAT | 55833 |
rs777216950 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037716 | AATAATTGAGAAAAT[A/C]ATCATCTGAGAAAAG | 55833 |
rs777239302 | in-del | -/AAAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33930896 | GTGAGACTGCATCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAGCG | 55833 |
rs777302127 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013547 | GTTATCTCAGAACAC[C/T]TCTAACATAACACTG | 55833 |
rs777306332 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015120 | TAGTCAAATCAATCT[C/G]CAAGTAAGACAAACT | 55833 |
rs777319237 | snp | A/G | 1.67424e-05 | 0.00289326 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989113 | TTCTTACACCCTACA[A/G]TCTCCCATGAAGTCT | 55833 |
rs777334467 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959922 | AAAAAAATCAATCCT[A/G]CTTAACACCTGGTAA | 55833 |
rs777339440 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982825 | GTACCCATCCTAACA[G/T]ATACTCAATCTCCAA | 55833 |
rs777377626 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924060 | GAGAAAGGCCACACT[A/G]GCTTCTGCAAACAGG | 55833 |
rs777414106 | snp | G/T | 1.65198e-05 | 0.00287395 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923763 | AGCAACCCAAGGCCA[G/T]GAGACACAGTCACAC | 55833 |
rs777416531 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047314 | TCACTTCTGCCTAAT[A/G]ATAAGAGAAGCCTTC | 55833 |
rs777417316 | snp | A/C | 0.000119653 | 0.00773383 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960782 | TGAAATTCCATTTCA[A/C]AAAAAAAAAAAAAGA | 55833 |
rs777466624 | snp | A/G | 6.58924e-05 | 0.0057395 | missense | UBAP2 | GRCh38.p7 | 9:33944450 | GAGATATTTTCAATG[A/G]TCGTGCTGGGAAGCT | 55833 |
rs777466848 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34030291 | TCTACTAAAAATACA[A/G]AAACAAAATTAGCCA | 55833 |
rs777467939 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946039 | ACATCCTTTTTAACA[C/T]ACTCTAATATCAAAC | 55833 |
rs777471668 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33947195 | ATCGCTTCAAACCCC[A/G]GAGTGGTCTCATGTA | 55833 |
rs777473045 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33958509 | GCCTCCCGGGTTCAA[C/G]TGATTCTCCTGCCTC | 55833 |
rs777496854 | in-del | -/TA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33976845 | CTACTAAAAAAAATG[-/TA]TATATATATACAAAA | 55833 |
rs777532369 | in-del | -/G | 0.000197778 | 0.00994234 | splice-acceptor-variant | UBAP2 | GRCh38.p7 | 9:33923480 | AGGCTGGAGGGACCT[-/G]GGGGGGGCAAGCAGA | 55833 |
rs777572660 | snp | A/C/T | 0.00016474 | 0.00907441 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924203 | TCCATTGAGCAAACT[A/C/T]ACCTGGATATGGATT | 55833 |
rs777594620 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945673 | ACAGACAGACAGACA[G/T]ACATATATATACACA | 55833 |
rs777620769 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005707 | GGAGAAAAGAAAGCA[-/T]AAGTGTCAAACACTG | 55833 |
rs777621890 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34001573 | GGCAAGCGGTTTGTG[-/C]CCCCAAGCACTTTTT | 55833 |
rs777651354 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997256 | TAGCATTTTCATCAC[G/T]AGAACGATCACAGAC | 55833 |
rs777670418 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33966439 | CCAGCCTGTGTGACA[C/G]AGTGAGACTCCATCT | 55833 |
rs777719442 | snp | A/G | 1.65438e-05 | 0.00287605 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948596 | CGGATGACTTTAAAA[A/G]GGGGATAAAAGAACA | 55833 |
rs777725441 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967259 | GTCTACAGATTCTTT[C/T]ACACAATCACAAAAA | 55833 |
rs777728045 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974590 | TTTATAAATTATATA[C/T]CTGATCACAGAGTAA | 55833 |
rs777751147 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978699 | GCAGGAGAATGGCGT[A/G]AACCCAGGAGGGGGA | 55833 |
rs777766656 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019335 | TTGAACCCAAGAGGC[A/G]GAGGTTGCAGTGAGC | 55833 |
rs777776117 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998298 | AGCTACTCAGGAGAC[C/T]GAGGCAGCAGGATAG | 55833 |
rs777841150 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032164 | GCTAATAAGTTGCCA[A/G]CTTAACATCCTCATC | 55833 |
rs777843607 | in-del | -/T | 0.000103304 | 0.00718619 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017022 | AAAAAAAAGGAAAAA[-/T]AAAAAAAAGAGTTCC | 55833 |
rs777845536 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33932881 | TTGCTCCTCAGATGC[A/G]AAAAGTGAAGACAGA | 55833 |
rs777851724 | snp | A/G | 1.8415e-05 | 0.00303433 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932677 | TGAACAAGTGACTCC[A/G]GATGAACAAGACGCA | 55833 |
rs777858314 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942425 | AATGTGAAAAAACTA[-/AAA]CAACAACAACAACAA | 55833 |
rs777863188 | snp | A/G | 1.69183e-05 | 0.00290841 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927816 | GGTCACCAAGGGCGC[A/G]GCCCTGCTACTGCTG | 55833 |
rs777869767 | snp | C/G | 3.30278e-05 | 0.0040636 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923076 | AGCAGTTGTTCCCAG[C/G]TCCAGGCTCCCCACC | 55833 |
rs777870224 | snp | A/G | 9.88419e-05 | 0.00702931 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33924261 | AAGCGCTGTGGGTGC[A/G]GCAAAGGGAATTCCA | 55833 |
rs777878760 | snp | C/G | 1.66585e-05 | 0.00288599 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953295 | GTTACCAGGCTCTGA[C/G]GAGAACAGGAGTTGA | 55833 |
rs777919779 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33961850 | CCAAATAACTGACCT[C/T]CTCATAAGTAAAATG | 55833 |
rs777946314 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929872 | AGCTGGGCCTGGTGG[C/T]GTGTGCCTGTAATCC | 55833 |
rs777947620 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979572 | AAGAGAGAAATTCCC[A/G]TCTCAAAAAATAAAA | 55833 |
rs777966037 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960038 | GGGCTCAAGAGATCC[C/T]CCTGCCTTAGCCTCC | 55833 |
rs777990038 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017743 | CATGCTGGCTAACAC[A/G]ATGAAACCCCGTCTC | 55833 |
rs778008870 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33997758 | GGCCAGTGTTCTATC[C/T]ATACTATTCAGATAA | 55833 |
rs778022608 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950682 | CTGATTTAATGAAGG[C/T]TTCCCAGGTGATGAC | 55833 |
rs778034027 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34046645 | CAAGACTCCATCTCA[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 55833 |
rs778072738 | snp | C/G | 3.29506e-05 | 0.00405884 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:33971719 | CCACACACATCTGTA[C/G]ATGTAGAATCTGAAT | 55833 |
rs778080374 | snp | C/T | 1.66996e-05 | 0.00288956 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933678 | TGTTTATTTCTAAAA[C/T]CAATCCTAAGTGCCT | 55833 |
rs778081223 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031420 | TCAAGCTATTCTCCT[A/G]CCTTGGCCTCCTGAG | 55833 |
rs778095970 | snp | C/G | 1.6477e-05 | 0.00287024 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996307 | CACTATGCATTCATC[C/G]TGATTTTTCCCTGTC | 55833 |
rs778118562 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984966 | TAAGCAAATTAAACA[A/G]ATGCTGGTGAAGATA | 55833 |
rs778148692 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993263 | AGAATCGTTTGCCTT[C/T]ATGCTCTTGCTCCTA | 55833 |
rs778162948 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027712 | ATACAAAAAAAAAAT[-/T]TAGCCGGGGGTGGTG | 55833 |
rs778188718 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949206 | AAAATAAAATAAAAT[A/G]ATAAAAAGTGATGTC | 55833 |
rs778200115 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980730 | GGAGTTTGAGGTGGG[C/T]GGGTTGTTTGAGCTC | 55833 |
rs778208011 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34023352 | CATATTCAATGTACA[C/T]TAATTTTTTGATTTA | 55833 |
rs778253785 | snp | A/C/G | 4.96186e-05 | 0.00498069 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998783 | TCCTTTGCCAGAAAC[A/C/G]TACCTGCTTAACTTT | 55833 |
rs778259377 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963816 | AATGTAAAATTGAGG[A/G]TTTAAACATATGAAA | 55833 |
rs778269121 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032754 | CATGTCAAAACCCTA[C/T]CTTTACAAACAATAC | 55833 |
rs778278565 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950102 | AGACAGTCTCGCTCT[A/G]TCACCCAGGCTGGAG | 55833 |
rs778284672 | snp | A/C | 1.64885e-05 | 0.00287123 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933609 | CGGGAGGGCAGAGGG[A/C]GGGCCTGTTGTCTTT | 55833 |
rs778286057 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935311 | GAAGTAGTTTCTTTC[-/T]TTTTTTTTTTTCTTT | 55833 |
rs778286352 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33968913 | TGCCTTAGACATTTC[A/G]GATAAATAAAATCAT | 55833 |
rs778289619 | in-del | -/AAAGC | 1.65919e-05 | 0.00288022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33943595 | AAGCTGGGATCTGAA[-/AAAGC]AAAGCTGTCGTGTCA | 55833 |
rs778322219 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021475 | TTATCATTTTGGTTG[C/T]ATTATAGAGAACAAG | 55833 |
rs778333262 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027476 | AACTCCAACAGTCTG[A/G]GAGGCCAAGAGGGGG | 55833 |
rs778338178 | snp | C/T | 3.29897e-05 | 0.00406125 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33944566 | AGGAGGAACAGTGAC[C/T]GCCTGGCTCTGGTGC | 55833 |
rs778354705 | snp | A/G | 1.72074e-05 | 0.00293316 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988931 | GGGAGGGTCACTTGA[A/G]ATGAAAGAAGAGAAA | 55833 |
rs778363999 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953644 | ATCCACACAAAAGAA[C/T]ATACCAAGCCACAGA | 55833 |
rs778394475 | snp | A/G | 0.000164734 | 0.00907413 | missense | UBAP2 | GRCh38.p7 | 9:33923958 | GGTGTGGTAGCGGGT[A/G]CAGGGGATGCAGAGT | 55833 |
rs778396687 | snp | C/T | 1.75336e-05 | 0.00296082 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922626 | GAGAAGGGAAGGCTG[C/T]CAAGGCTGGAGCAGA | 55833 |
rs778437596 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041605 | GGGAGGCCGAGGCAG[A/G]AGAATTGCTTGAACC | 55833 |
rs778465026 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014256 | CGCCTGAACCCCAGA[A/G]GCGGAGGTTACAATG | 55833 |
rs778499089 | snp | C/T | 1.80127e-05 | 0.003001 | missense | UBAP2 | GRCh38.p7 | 9:33922790 | TAGCCAGGGGCCGCT[C/T]CCGAGGCCAGGGGCC | 55833 |
rs778529824 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33937266 | AATTTAACTGCGTCT[A/G]GGGTGTAAATAAGTA | 55833 |
rs778536547 | snp | A/G | 1.64743e-05 | 0.00287 | missense | UBAP2 | GRCh38.p7 | 9:33923466 | CATGTTGCTTGGCTG[A/G]GGCTGGAGGGACCTG | 55833 |
rs778538368 | snp | C/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049974 | CCTGTTTGGATGTGA[C/G]GGCGTTCTGGCTATC | 55833 |
rs778573787 | snp | C/G | 1.64784e-05 | 0.00287035 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33989013 | TCCTTTCCGGTTGTT[C/G]TTTCCACGTCCACGA | 55833 |
rs778585730 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965989 | CGGGAGGCAGAGCCT[A/G]CAGTGAGCAGAGATC | 55833 |
rs778616705 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33924735 | GCCAGGTAGGCACGG[A/G]AATAAGCAGGACCCC | 55833 |
rs778636233 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977448 | ACGCTACTAGTAACA[C/T]TGGTTTCTGTGTATA | 55833 |
rs778644466 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33946221 | TTGATCTGCTTTATT[G/T]TTACTCTTTTTATAT | 55833 |
rs778645401 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923359 | ACCCCATGTGTCTCT[A/G]TCTGGGAAGTACCCC | 55833 |
rs778652261 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953435 | TTCTGAGGCTTGACT[A/G]TGAGGAACAGGCTTC | 55833 |
rs778668848 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989208 | ATGTATCTTTCTTTT[-/TT]TTTTTTTTTTTGAGA | 55833 |
rs778695018 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970205 | CCTAATATCTATATG[A/T]TCCATATCAATATTC | 55833 |
rs778708910 | snp | C/T | | | | | GRCh38.p7 | 9:34029940 | TGCAGTGAGCTGAGA[C/T]TGCGCCACTGCACTC | 55833 |
rs778716280 | snp | G/T | | | | | GRCh38.p7 | 9:33931311 | TATGGAGGGACAACT[G/T]TATTAGCAATGTCAC | 55833 |
rs778718493 | snp | C/T | 1.64944e-05 | 0.00287175 | | | GRCh38.p7 | 9:33924158 | CCAGCTCCTGGAGTT[C/T]GCGCTAGGCCGGCCC | 55833 |
rs778727323 | snp | C/G | | | | | GRCh38.p7 | 9:33964555 | CACACTGTGTGGAAG[C/G]TGTGCACAGTGGTGC | 55833 |
rs778756554 | snp | A/C | | | | | GRCh38.p7 | 9:33983258 | TTAAACATGTCTCTA[A/C]ACAACCAATCCAAAT | 55833 |
rs778771608 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970240 | TCTCCTTCCTGGAAC[C/T]AATTATTCACGTTCT | 55833 |
rs778777320 | snp | A/C | 0.000115316 | 0.00759243 | intron-variant, missense | UBAP2 | GRCh38.p7 | 9:34017091 | TTGATTGTGCTGCTG[A/C]AATCTGTGGTTTTTC | 55833 |
rs778781030 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008199 | GGCGCATGCCTGTAA[C/T]CCCAGTTACTTGGGA | 55833 |
rs778788867 | in-del | -/CC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045463 | CAGCAACCTCCACCT[-/CC]CCCAGGTTCAAGCAA | 55833 |
rs778891310 | snp | C/T | 1.648e-05 | 0.0028705 | missense | UBAP2 | GRCh38.p7 | 9:33943516 | GGTTCTGACCCAAAT[C/T]CCAGAGCCCCAAACT | 55833 |
rs778908999 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945563 | ATTATGTTTCTCTTC[C/T]ACACCACTCTCCCAT | 55833 |
rs778913693 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996179 | AAATGTGCTACGGAA[C/T]TGGAGACAAATGTAA | 55833 |
rs778929387 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022864 | TGAGTAGTTTACTCA[C/T]AGATTTCCAGTTCTG | 55833 |
rs778932849 | snp | A/G | 3.29489e-05 | 0.00405874 | intron-variant, synonymous-codon | UBAP2 | GRCh38.p7 | 9:33973194 | TTACCCCATGCCTTG[A/G]GTTGAGAACCTTCCT | 55833 |
rs778937022 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33948567 | TGCAAGCTCTCCAAA[C/T]CCTGAGCCAAGGACG | 55833 |
rs778959941 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045957 | TGGAAAAAACGGCTG[C/T]TTCTAAAATCTATCA | 55833 |
rs778972139 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | UBAP2 | GRCh38.p7 | 9:33924254 | GGCTGGCAAGCGCTG[C/T]GGGTGCAGCAAAGGG | 55833 |
rs778975821 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33977042 | GTTGTTTTTTATTTA[-/TT]TTTTTTTTTTTTTTG | 55833 |
rs778989408 | snp | A/G | 1.66308e-05 | 0.00288359 | intron-variant | UBAP2 | GRCh38.p7 | 9:33944335 | AATAATTCCAGCTTT[A/G]GGACGGTGACTTCAT | 55833 |
rs778996699 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953211 | AGTAATTATAAAGCA[C/T]GTATCATATTCTAGA | 55833 |
rs779003309 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924191 | GGCTACTCCTCATCC[A/G]TTGAGCAAACTCACC | 55833 |
rs779010270 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017528 | AACCCCAAAACAACA[C/T]TGCACCCAGCCAAGA | 55833 |
rs779033546 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941643 | AAAAACTAAAATACC[A/G]CTTACCATGATGGTT | 55833 |
rs779045926 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015970 | CACTATGCCCAGCAA[A/T]GGCAGCTTTTTAAAG | 55833 |
rs779056420 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972814 | ACTAAAATGGCTCTT[A/G]GGCAGTGCCATTTAG | 55833 |
rs779078029 | snp | A/G | 1.66067e-05 | 0.00288151 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922920 | AGGTCAGGTTGGGCT[A/G]TAACCTCTCAAAAAC | 55833 |
rs779087844 | snp | C/T | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921986 | TCCCAGATGAAGATT[C/T]GGTGGAAGGAGACCA | 55833 |
rs779116876 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34029037 | GGTAGGAATCCTTGA[G/T]CTTAGGAGATCAAGG | 55833 |
rs779125529 | snp | A/G | 1.75987e-05 | 0.00296631 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989168 | TTTATCATTCAAAGT[A/G]TGTACAATTATCAAA | 55833 |
rs779168295 | snp | C/G | 1.64961e-05 | 0.00287189 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923060 | AGCAGTTGTTCCCCA[C/G]AGCAGTTGTTCCCAG | 55833 |
rs779177446 | snp | C/T | 4.9498e-05 | 0.00497459 | missense | UBAP2 | GRCh38.p7 | 9:33941654 | TACCACTTACCATGA[C/T]GGTTCCTGGAGCTGA | 55833 |
rs779201585 | in-del | AAGGAAGGGTGGAAGGGGGGAAGCG/GT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33981800 | AGGAAGGAAGGAAGG[AAGGAAGGGTGGAAGGGGGGAAGCG/GT]GGGAAGGAGGGAAGG | 55833 |
rs779208392 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047235 | GTCACACGTATCAAC[C/T]AGCCATAAGTAGGAA | 55833 |
rs779250903 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996970 | CCCTGGAGGTGAAGG[G/T]TGCAATAAGCCATGA | 55833 |
rs779273074 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973451 | AAAAGAATTAAATTA[C/T]CCTTGTATTATATTT | 55833 |
rs779275162 | in-del | -/G | 8.23635e-05 | 0.00641677 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923363 | CATGTGTCTCTGTCT[-/G]GGAAGTACCCCTCAC | 55833 |
rs779275870 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004408 | AGGATCACCTTAGCC[C/T]GAGGAGGTCAAGGTT | 55833 |
rs779301983 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33940577 | TGAACCCAGCAGTTC[A/G]AGATCAGACTGGGCA | 55833 |
rs779317770 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003509 | TTCCCAGGTTCAAGC[A/G]ATTCTCCAGCCTCAG | 55833 |
rs779318902 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037825 | AATACTTCAGTGACA[A/G]TATGTAAATACAGAA | 55833 |
rs779320093 | snp | C/G | 1.6495e-05 | 0.0028718 | intron-variant | UBAP2 | GRCh38.p7 | 9:33963800 | GCCAGTTCTGTGGAC[C/G]AATGTAAAATTGAGG | 55833 |
rs779338099 | snp | C/T | 3.29565e-05 | 0.00405921 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960893 | CCTGTTGGGAAACAA[C/T]AGCAATCAAAGTTTA | 55833 |
rs779369751 | in-del | -/ATCAGCATTTTATTAAATGCT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33978164 | GTAACTGATTTGAGA[-/ATCAGCATTTTATTAAATGCT]ATCAGCATTTTATTA | 55833 |
rs779372036 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34025123 | ACATGGAAACTAGAC[C/T]GTAAAAATCAACACC | 55833 |
rs779384156 | snp | A/T | 3.29495e-05 | 0.00405877 | missense | UBAP2 | GRCh38.p7 | 9:33941717 | TCCTGTTATGCACAG[A/T]ACTCTGGTCATAAGA | 55833 |
rs779395548 | snp | A/C | 1.73812e-05 | 0.00294793 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922615 | CTGAGGAAGAGGAGA[A/C]GGGAAGGCTGTCAAG | 55833 |
rs779400925 | snp | A/G | 0.000131794 | 0.00811661 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996285 | CTCCATTACAATCAT[A/G]TAGGGCCACTATGCA | 55833 |
rs779402002 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963670 | AAAAATGAAAGATAT[C/T]GCAAGCAATTTATAA | 55833 |
rs779405055 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33991769 | AAAACAGAATCCAGT[C/T]CTCTTAGGTTAGAAT | 55833 |
rs779429504 | snp | C/T | 6.58946e-05 | 0.0057396 | missense | UBAP2 | GRCh38.p7 | 9:33944475 | GAAGCTGCAAAAGCT[C/T]GTTCACAGTGGAGGG | 55833 |
rs779448177 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005437 | AAGACCCTGTCTCAA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs779466869 | snp | C/G | 1.82453e-05 | 0.00302032 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33927079 | GTTTGGGGGTGCTTT[C/G]CCTGTATAGAGGGAA | 55833 |
rs779475163 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045777 | AAAATTGTAAAAACT[A/C]ATCTGATAAATTTGA | 55833 |
rs779501664 | in-del | -/AC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019698 | TTACTACACACACAC[-/AC]ACACACACACACACA | 55833 |
rs779514403 | in-del | -/CTG | 1.66932e-05 | 0.002889 | cds-indel | UBAP2 | GRCh38.p7 | 9:33927825 | GGCGCGGCCCTGCTA[-/CTG]CTGCTGCTGGATGCA | 55833 |
rs779538495 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936697 | GAGACAATACCACTA[A/T]AGATCTCAGAAACAT | 55833 |
rs779554430 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928615 | TGACAAGGTACCCCT[A/G]TGAAGAAAGAGTGAA | 55833 |
rs779590514 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026020 | TTAAAGCTTACATAA[A/G]CACAAATTCATCTAA | 55833 |
rs779612668 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33998914 | CCAAAAGCATAAGTT[-/A]AGATTCCAAAATCTG | 55833 |
rs779628071 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962863 | CACACCTGTAAATCC[C/T]GGCTACTTGGGAGGC | 55833 |
rs779664280 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | UBAP2 | GRCh38.p7 | 9:33926660 | AGCTCGTCATAGCCA[C/T]AGATCTGTGTGAGAA | 55833 |
rs779665134 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33933597 | GGAGCTCACAGACGG[A/G]AGGGCAGAGGGAGGG | 55833 |
rs779685532 | snp | C/T | 3.70377e-05 | 0.0043032 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935733 | AGGGCTGCTTTTTAA[C/T]GAATAAGCCATTGAC | 55833 |
rs779699205 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938797 | CAAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs779701689 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34012668 | GTATTAAGTGAAGAA[C/G]AACCTTATTCACAAC | 55833 |
rs779715742 | in-del | -/AGAAGT | 1.64879e-05 | 0.00287118 | cds-indel | UBAP2 | GRCh38.p7 | 9:33948423 | GGGCTTGAGGTCCCA[-/AGAAGT]AGTAGTTGTAGGGTG | 55833 |
rs779722539 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970122 | TTTTTTTTGCAGAGA[C/T]GGAGTTTCACCATGT | 55833 |
rs779739415 | snp | A/G | 1.81352e-05 | 0.00301119 | missense | UBAP2 | GRCh38.p7 | 9:33922691 | ACTGTACTCACCTGT[A/G]CATCCTGCGGAAGGT | 55833 |
rs779741753 | in-del | -/ACT | 1.64751e-05 | 0.00287007 | intron-variant, cds-indel | UBAP2 | GRCh38.p7 | 9:33971689 | TGAGCAGCTTCCCAA[-/ACT]ACTAGCTTTGTCCCA | 55833 |
rs779752046 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | UBAP2, SNORD121B | GRCh38.p7 | 9:33934324 | GTCTCAGTGCTGTCC[A/G]CACATACAACTCAGA | 55833 |
rs779753519 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031883 | GGTTCATGCCCGTAA[C/T]CTCAACACCTTGGGA | 55833 |
rs779760081 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926583 | TGTAAAAGATTCTGA[A/G]CCCTCTGCTCCGACC | 55833 |
rs779762489 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006302 | CACTGGACAACTAGG[C/T]AGAAATGTCAAGAGA | 55833 |
rs779772968 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953427 | GAGTTGGCTTCTGAG[C/G]CTTGACTGTGAGGAA | 55833 |
rs779774116 | snp | A/G | 1.64882e-05 | 0.00287121 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923520 | AGTGTAGGAAGAGGC[A/G]AGCTGAGGCTGGTCA | 55833 |
rs779775169 | in-del | -/TAAG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011503 | TTTTAATGAGAACTT[-/TAAG]TATTTTTTTTAACTT | 55833 |
rs779777525 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987390 | GCACTCCAGCCTGGG[A/C]AAGTGAGCAAGACTC | 55833 |
rs779783634 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033622 | TGACTCTTTCGCCCA[A/G]GCTGAAGCGCAGTGG | 55833 |
rs779795204 | snp | C/T | 6.80828e-05 | 0.0058341 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941892 | AAATATTCAACATAA[C/T]TTTGTTACTTTAAAT | 55833 |
rs779806586 | snp | C/T | 1.64751e-05 | 0.00287007 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33986786 | GCTCGCTTGCCACGA[C/T]CTGAAGGTTTGTCCA | 55833 |
rs779821759 | snp | A/C | 6.58924e-05 | 0.0057395 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923346 | GCAAGCCTGTCTAAC[A/C]CCATGTGTCTCTGTC | 55833 |
rs779833256 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979479 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 55833 |
rs779878460 | in-del | -/GA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33950509 | TCCTAACTTCGCTTT[-/GA]GAGTAAAACATTAGG | 55833 |
rs779941549 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923267 | AGTAGTCTCCTGCTG[C/T]TGTCCCCTGGGTCAG | 55833 |
rs779944551 | in-del | -/AAGA | 3.40959e-05 | 0.00412878 | intron-variant | UBAP2 | GRCh38.p7 | 9:34017194 | AAATAGAAAATCTGC[-/AAGA]AAGTAGGGATGGTAA | 55833 |
rs779951458 | in-del | -/AAAAAAAAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013153 | GTGAGACTCTAGCTC[-/AAAAAAAAA]AAAAAAAAAAAAAGA | 55833 |
rs779967874 | snp | C/T | 6.61124e-05 | 0.00574907 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986884 | CCATTTCCAAACCTC[C/T]TGTACATAACCTTAT | 55833 |
rs779997178 | snp | A/G | | | upstream-variant-2KB | UBAP2 | GRCh38.p7 | 9:34049686 | CTGGGTGAAAAGACT[A/G]GAATCTACTGAACGC | 55833 |
rs780000688 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33963084 | TTTGGACTTGCATAA[C/T]AGGGTGAGAATCTGA | 55833 |
rs780001768 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994249 | AGGTTCGGTCCCAAA[A/G]GAGGAGGGGGTGTTA | 55833 |
rs780008676 | in-del | -/GGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016246 | AGGAAGGGGAGGAAG[-/GGA]AGGAGGAGGAGGAAG | 55833 |
rs780035864 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957154 | CGATGTTTTCTCCCC[A/C]CAAAGACAGATGTCT | 55833 |
rs780043484 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34022759 | CTCCTTAAATAAATA[C/T]ATTTTAAGAAAAGAA | 55833 |
rs780070478 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33943494 | TGATCCAAATTCAGA[A/G]AGAGAAGGTTCTGAC | 55833 |
rs780084527 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973169 | ATTATAAAAATAGGA[C/T]GGCTATCACTTACCC | 55833 |
rs780107809 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34045616 | CGACCTCGTGACCCG[C/T]CCGCCTCCGCCTCCC | 55833 |
rs780125005 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33996111 | AACTTAAAACAAATA[C/T]GGAATGGCACCATAA | 55833 |
rs780149323 | snp | C/T | 9.97274e-05 | 0.00706072 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998901 | TAAGGATTTGAACAC[C/T]AAAAGCATAAGTTAG | 55833 |
rs780150470 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34032532 | ATATCAAAATATAGG[C/T]TAACCTACCTCAGCT | 55833 |
rs780155224 | snp | A/G | 1.77704e-05 | 0.00298075 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927996 | CACACTGGCATGCTG[A/G]CAAAAGAAAAGCCAG | 55833 |
rs780155615 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931846 | TGCCTACTCCAACCT[C/T]GCCCAACACCTCCTG | 55833 |
rs780175457 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33982695 | ATCTAGCATACTTGC[A/G]ATTAAGAAAAACTAT | 55833 |
rs780207289 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33975157 | GTGTTGGCGGCCGGG[C/T]GTGGTGGCTCACGCC | 55833 |
rs780231721 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34014979 | ACCAGCAGAATACTA[C/T]ACTAACTTTATACTG | 55833 |
rs780244782 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33959196 | TTTACAAGGTAAAAT[A/G]AATCTATCTATGGTA | 55833 |
rs780246057 | snp | A/C | 1.64887e-05 | 0.00287125 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924049 | TCCTCCAACCAGAGA[A/C]AGGCCACACTGGCTT | 55833 |
rs780265088 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003377 | ACATCAAAGATGGCT[-/TT]TTTTTTTTTTTTTGA | 55833 |
rs780266624 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924178 | TAGGCCGGCCCCGGG[C/T]TACTCCTCATCCATT | 55833 |
rs780272524 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044540 | GCACTCCAGCCTGGG[C/T]GACAGAGAAAGACTG | 55833 |
rs780320254 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34036983 | CACCACACCCAGCTA[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs780351953 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008071 | ACCTGGGAGGCGAAG[A/G]TTGTAGTGAGCCGAG | 55833 |
rs780357359 | in-del | -/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992655 | AGACAACTTATCGGG[-/C]GGAGGGGGGGGGGCA | 55833 |
rs780358226 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34004799 | CAAAAAAAAAAATAG[C/G]GAAAAAAAAAGTAAA | 55833 |
rs780378165 | in-del | -/CAAAT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33936664 | CAAAACAAAACAAAA[-/CAAAT]CAAATAAATAAATAA | 55833 |
rs780396882 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017301 | TCTCTGGAATACAAA[A/T]TCTCAAGAAGTAGCC | 55833 |
rs780422167 | in-del | -/TAATG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34037458 | ACCTTAAGTTTTTAC[-/TAATG]TAATTGTTGCCTCAC | 55833 |
rs780423431 | snp | A/G | 1.66474e-05 | 0.00288503 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922917 | TGAAGGTCAGGTTGG[A/G]CTGTAACCTCTCAAA | 55833 |
rs780426717 | snp | A/C/G | 8.80963e-05 | 0.00663636 | missense | UBAP2 | GRCh38.p7 | 9:33927072 | GAGGTAAGTTTGGGG[A/C/G]TGCTTTGCCTGTATA | 55833 |
rs780427443 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33928462 | GAGATTTCCCTTCTA[C/T]TGGGATTCTCAGCCA | 55833 |
rs780441132 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33927453 | GTCGGTTTTAGCAGC[A/G]ACCATCAAATCATAG | 55833 |
rs780459040 | snp | C/G | 1.6473e-05 | 0.00286988 | missense | UBAP2 | GRCh38.p7 | 9:33948469 | TTCTGCTGTGTACTT[C/G]GGGTGGTGGTAAACT | 55833 |
rs780473532 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34039933 | GGAGGCCGAGGCGGG[C/T]GATCACCTGAGGTCG | 55833 |
rs780479195 | snp | A/G | 1.70886e-05 | 0.00292301 | intron-variant | UBAP2 | GRCh38.p7 | 9:33989137 | GAAGTCTATCAGAGA[A/G]AACGGCTGTTAATCA | 55833 |
rs780482546 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33960110 | AATTTTTTTATTATT[A/T]TTTTTTTTGTAGAGA | 55833 |
rs780499690 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34002076 | CTCCTCTGACCTCAG[A/C]CTCCTGAGTAGCAAC | 55833 |
rs780518899 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923776 | CAGGAGACACAGTCA[C/T]ACCCTCTGAAATACT | 55833 |
rs780519998 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33983565 | ACACACATAACGTTG[G/T]TCTTATACTGTGACC | 55833 |
rs780521694 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971396 | TGTGGGTTTGTGCTG[A/G]TTTATGCCAATTACC | 55833 |
rs780545586 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942533 | CAGAGTTTGAGGCCA[A/G]TCTGGGCAACATGAC | 55833 |
rs780567035 | snp | A/G | 0.0295041 | 0.11782 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960796 | AAAAAAAAAAAAAAA[A/G]AAAGGTCTCATCTGA | 55833 |
rs780576084 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33967563 | CATAGATCTTATTGT[C/T]CAGGAAACAGTCATA | 55833 |
rs780585327 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34003627 | ATTCAGGCTGGTCTT[G/T]AACTCCTGACCTTAA | 55833 |
rs780594934 | snp | C/T | 1.66515e-05 | 0.00288539 | missense | UBAP2 | GRCh38.p7 | 9:33927011 | GCAGGAAGCAGTCCT[C/T]CGGGACCTACGAGGT | 55833 |
rs780595914 | in-del | -/A | 6.58924e-05 | 0.0057395 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923317 | CAGGGTACAAGAGGC[-/A]AAGTGTGAGCCAGGC | 55833 |
rs780602087 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935859 | AGTGTCTGCTGACTT[C/T]GACCACCACCATGTC | 55833 |
rs780605148 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33926560 | CCAAGACCATAAGAG[G/T]GGGGACATGTAAAAG | 55833 |
rs780615956 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34010933 | GTATGGCTGAAATCT[C/T]TGTGGAAAAAGTATG | 55833 |
rs780616533 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | UBAP2 | GRCh38.p7 | 9:33948554 | CCATTTTTGGTGGTG[C/T]AAGCTCTCCAAATCC | 55833 |
rs780624403 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989418 | GTGTTAGCCATGATG[C/G]TCTCGATCTCCTGAC | 55833 |
rs780652449 | snp | A/G | 1.64808e-05 | 0.00287057 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33996245 | GAATTCCCTTCCAGC[A/G]ATATATTGATAGCTT | 55833 |
rs780691716 | in-del | -/TATT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33999948 | TCGCCCAGGCTGGAG[-/TATT]TATTTATTTATTTTG | 55833 |
rs780691853 | snp | A/G | 3.48268e-05 | 0.00417279 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941612 | ATTTCCAAATAAGAC[A/G]GACATCTTCTGAGAA | 55833 |
rs780703688 | in-del | -/TT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021635 | AGAATCCATTTGATT[-/TT]TTTTTTTTTTTTTTT | 55833 |
rs780740846 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960881 | TTCTTCCAAGCCCCT[A/G]TTGGGAAACAACAGC | 55833 |
rs780751571 | in-del | -/C | 0.000449104 | 0.0149783 | intron-variant | UBAP2 | GRCh38.p7 | 9:33922605 | CGAGCCACTCTGAGG[-/C]AAGAGGAGAAGGGAA | 55833 |
rs780754853 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938972 | AAGAGAAAAAGGAAG[A/G]GAGGATGATCCATCC | 55833 |
rs780776722 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33945622 | CCGGTTTTCCTGAAT[A/G]TCTCTTTCAGAGATA | 55833 |
rs780789852 | snp | A/T | 1.79496e-05 | 0.00299574 | synonymous-codon | UBAP2 | GRCh38.p7 | 9:33922519 | TTAGTTTGTCCAGTA[A/T]GGAGAGTTGCCGTAG | 55833 |
rs780813979 | in-del | -/T | 1.77038e-05 | 0.00297516 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932651 | CAAAACAGAGCGCCG[-/T]TATGTCCACCTGAAC | 55833 |
rs780869129 | in-del | -/G | 0.000132083 | 0.00812552 | frameshift-variant | UBAP2 | GRCh38.p7 | 9:33944586 | GGCTCTGGTGCTGTT[-/G]TCGCTGGCTCAACTG | 55833 |
rs780886083 | snp | A/C | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922372 | GCCAGTCTGGGAGGC[A/C]GACTCCCCACAGAGG | 55833 |
rs780888122 | snp | A/G | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934073 | GCTTCCGCCAAGTCA[A/G]GCTGACTCTACCAAT | 55833 |
rs780898966 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34019613 | GTGGTTGCACGACAA[C/T]GTAAATGTACTTAAT | 55833 |
rs780917167 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985629 | TTATCTCATGCAGGT[A/G]GAGAGTGGAATGATA | 55833 |
rs780923321 | snp | C/T | 1.65707e-05 | 0.00287838 | missense, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953311 | GAGAACAGGAGTTGA[C/T]GGCAGTGGAGCTGCC | 55833 |
rs780928445 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34016912 | TTTCCTACAAAGGAA[A/G]ACATTAAATCATATG | 55833 |
rs780976480 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34033867 | CAGCCTCCCAAGTAG[C/G]TGGGATTACAGGCAC | 55833 |
rs780986638 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34048084 | TAGACTAAAAACTCA[G/T]GGGAAAATGTGGAAA | 55833 |
rs780989634 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33985050 | CATTTTGGAAAACAG[C/T]ATGGAGATTTATCAA | 55833 |
rs781003730 | in-del | -/ATT/ATTA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33962686 | ATAAATAAATAATTA[-/ATT/ATTA]AAAAATAGGGCCTGG | 55833 |
rs781012536 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33943099 | AATGAAATATTTGGC[A/G]ATAAAAATGATACAT | 55833 |
rs781033276 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026281 | GCATTGATTGGAAGA[C/T]AGTTCTAAAACCAGG | 55833 |
rs781040054 | in-del | -/TATT/TATTTATTTATG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34028362 | CTGTAAACCCTGTCT[-/TATT/TATTTATTTATG]TATTTATTTATTTAT | 55833 |
rs781086844 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938796 | GCAAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs781114292 | snp | A/C | 1.65051e-05 | 0.00287267 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986863 | AAGAGCAGAAAAATC[A/C]AATTTCCATTTCCAA | 55833 |
rs781133662 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031624 | AACTTGCTTTCCTAA[C/G]TAAATTCAAGCGATT | 55833 |
rs781135846 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33973718 | TTATGACTAGCACCT[C/T]TCCACATTCTCTTCA | 55833 |
rs781149445 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955985 | TAAAAAGGGAAAAAA[C/T]AGAAAGAGACCCAAA | 55833 |
rs781159238 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34013927 | GCCACTTTTTATGAC[A/T]CCAATTTAAGATTAC | 55833 |
rs781171344 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34044243 | TGTCTCTACTAAAAA[A/T]ACAAAAAATTAGCCA | 55833 |
rs781179164 | snp | C/T | 3.29565e-05 | 0.00405921 | missense | UBAP2 | GRCh38.p7 | 9:33924275 | CAGCAAAGGGAATTC[C/T]ATAGTAGTCCTAGGA | 55833 |
rs781214085 | snp | A/G | 1.65743e-05 | 0.00287869 | intron-variant | UBAP2 | GRCh38.p7 | 9:33998878 | GCCTGGAAAGTACAT[A/G]CAATTGTTAAGGATT | 55833 |
rs781224208 | snp | A/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33987794 | AATTTGCTCATTAAT[A/T]AGGTTCAAAGCCTGG | 55833 |
rs781235654 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935793 | ATCCTCTTCCTCTGT[C/T]TGGTTGGCACCAGCC | 55833 |
rs781238137 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34047460 | CCAATGTAGGATACG[C/G]GAGAGCTTAGGTATC | 55833 |
rs781253292 | in-del | -/C | 1.65982e-05 | 0.00288077 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922440 | CTGGGCTCCCAAATA[-/C]GTGCTCGTGTGTTCT | 55833 |
rs781260546 | snp | A/G | 0.000560067 | 0.0167248 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923181 | AAAGGAGAGGTAAAC[A/G]CTACCTTTGCCAGGC | 55833 |
rs781267009 | snp | A/G | 1.65679e-05 | 0.00287814 | intron-variant | UBAP2 | GRCh38.p7 | 9:33924336 | CCTGCTTGACTCCCA[A/G]GAGAGCAGAACCAGC | 55833 |
rs781267472 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34018937 | ATTCATAATAGCCAA[A/G]AAGTGGAAGATACCC | 55833 |
rs781269139 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | UBAP2 | GRCh38.p7 | 9:33923166 | CAGGCCTTATCCTGG[A/C]AAGGAGAGGTAAACA | 55833 |
rs781276023 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006134 | GCTACTTGGAAAGCC[C/G]AAGCAGGAGAATCGC | 55833 |
rs781292773 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | UBAP2 | GRCh38.p7 | 9:33923249 | CAGCATAGCCACCTT[C/T]GGAGTAGTCTCCTGC | 55833 |
rs781302192 | snp | G/T | 1.66319e-05 | 0.00288369 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941873 | GCTCACTGAAAAGAG[G/T]CAAAAATATTCAACA | 55833 |
rs781312061 | in-del | -/AAAAC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33942423 | GAATGTGAAAAAACT[-/AAAAC]AAAACAACAACAACA | 55833 |
rs781314673 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33993545 | AGCGTAGTGGCATGC[A/G]CCTGTGGTCCCGGCT | 55833 |
rs781319828 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041894 | GCCAGGCATGGTGGC[A/G]GGCACCTGTAGTCCC | 55833 |
rs781344326 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951675 | AAAGATTAGAGTAGG[G/T]TCGAGAACCACTGCT | 55833 |
rs781345411 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34040525 | GTGAGGTGGGAAGAT[A/C]ACTTGAGCCCAGGAG | 55833 |
rs781386212 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33944308 | TAGTATCCCACTAGA[A/G]CTGAATGTAAAAATA | 55833 |
rs781392003 | snp | A/G | 3.29837e-05 | 0.00406088 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927907 | GACAGGCTGGCGCCT[A/G]AGGATGCGGAACTTG | 55833 |
rs781395903 | snp | C/T | 1.65094e-05 | 0.00287305 | utr-variant-5-prime, missense | UBAP2 | GRCh38.p7 | 9:33998824 | TCTGAATCATTCTTA[C/T]CAAAGATCACTTGAG | 55833 |
rs781438354 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33964123 | GCCTTCTGAGTATAC[A/C]CAAGTCTTTCTAGTT | 55833 |
rs781461180 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34042853 | TAGGCCAAGGCAGGA[A/G]GATCACTTTAGCCTA | 55833 |
rs781462733 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34026458 | CAGGATACACAATTT[A/G]TGTTAAAGAAGCAAG | 55833 |
rs781544354 | snp | C/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33974762 | TTCAAAACCAACCTG[C/G]CCAACGTGGCAAAAC | 55833 |
rs781549787 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33951828 | TTCAGTGGACACACA[C/T]AGATTTCAGCAAGGG | 55833 |
rs781558288 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935823 | CATGACAAGAGTAGC[C/T]TGCTGCTATACTTAC | 55833 |
rs781568658 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33938023 | TTTGTTTTGAGACAG[G/T]GTCTGGCTCTGTCAC | 55833 |
rs781625912 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33971241 | CCTGCAGAGGCAACG[C/T]TGCTACAAACCCATC | 55833 |
rs781646782 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33980981 | TACAGTAAATAAAAA[C/T]GGTGAGCCACACGAA | 55833 |
rs781659667 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953824 | AATATTTTACCCATT[C/T]ATTACCTAAAACCAG | 55833 |
rs781701472 | snp | A/G | 1.79858e-05 | 0.00299876 | missense | UBAP2 | GRCh38.p7 | 9:33922802 | GCTCCCGAGGCCAGG[A/G]GCCCAGTGGAGCCCA | 55833 |
rs781717518 | snp | A/G | 1.65272e-05 | 0.0028746 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935754 | AGCCATTGACCAACT[A/G]GTGTTTTCCACATCA | 55833 |
rs781722369 | snp | A/C/G | 0.000122976 | 0.0078406 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948344 | GAAACGTCCTCAGTA[A/C/G]GGGCAAACCCACAAA | 55833 |
rs781728470 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34015413 | AACCTCTGCCTCCCG[G/T]GTTCAAGCAATTCTC | 55833 |
rs781751616 | in-del | -/AAA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992389 | GCAAAACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 55833 |
rs781770326 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027528 | TTTAAAACCAGCCTG[A/G]GCAACACAGTGAGAC | 55833 |
rs781775634 | in-del | -/CGGA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33992655 | AGACAACTTATCGGG[-/CGGA]GGGGGGGGGGCACAA | 55833 |
rs796069570 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33957276 | ACACATCCAATAAAC[C/T]GCAAATATTCAAACC | 55833 |
rs796078039 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34008319 | GCGAAACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs796094555 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34000701 | GAGTTTTTTATATAC[A/G]CTCATTTCAAATAAT | 55833 |
rs796106802 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989204 | ATGCATGTATCTTTC[-/T]TTTTTTTTTTTTTTT | 55833 |
rs796202490 | snp | A/C | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34011315 | TTTATTCAGACTTAG[A/C]TTTTTCAGCTTAAGT | 55833 |
rs796236802 | in-del | -/TTT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34021649 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGGCTCGC | 55833 |
rs796376965 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34031278 | GCAAAACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 55833 |
rs796397170 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017927 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 55833 |
rs796434956 | in-del | AG/GGC | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955449 | CTTGAACTCAGGACG[AG/GGC]GGGGTTGCAGTGAGC | 55833 |
rs796448282 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33929169 | AACTGCCACAGAAAT[C/T]TGGAGCAGCTCTGAC | 55833 |
rs796448872 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33979810 | GAGGCGGAGGTTGCA[A/G]TGAGCCGAGATTGCA | 55833 |
rs796470124 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33984029 | GTGCCTCAGCGTCCC[A/G]AGTAGCTGGAACTAC | 55833 |
rs796493341 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33941916 | TTTAAATAGCTTCAT[-/A]AAAAAAAAAAAACAT | 55833 |
rs796617560 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33955682 | AATACAAAATTAGCT[CA/TG]GCGTGGGGGCGCATG | 55833 |
rs796633609 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33965154 | TCCGTGTTAAAACAG[A/G]AAATTTACCATTTCT | 55833 |
rs796638972 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33931782 | GTTCATCAGTTTCCT[A/G]CCTCCTCCATTCGTC | 55833 |
rs796647795 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027875 | TCAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAATC | 55833 |
rs796648745 | in-del | -/CA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041298 | GCTCTACTAAAAATG[-/CA]AAAAAAAAAAAAAAA | 55833 |
rs796677372 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33949705 | TTAGACTCGTCTCTC[A/G]TGTGTGTGTGCGCGC | 55833 |
rs796696231 | in-del | -/GT | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33994712 | TTGTCTTGTGTACCA[-/GT]GTTCTCTTACATGGA | 55833 |
rs796704364 | snp | G/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34005114 | CTAAAAATACAAAAA[G/T]TAGCAGTGCGTGGTG | 55833 |
rs796717596 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33972652 | AGCAACAAAAAGTAA[A/G]AAAACACCCAGAAAC | 55833 |
rs796733793 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006681 | GTGAGACCTTGTCTC[-/A]AAAAAAAAAAAGATA | 55833 |
rs796750620 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33989780 | TCTATTAGGCCTTAA[A/G]TCTACTTATTAATTC | 55833 |
rs796826876 | in-del | -/AG | | | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33922036 | CAGTTTCTCAAAAAC[-/AG]AGGTATGAAGTAATT | 55833 |
rs796844913 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041299 | CTCTACTAAAAATGC[-/AA]AAAAAAAAAAAAAAA | 55833 |
rs796874509 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34006238 | ACTCATCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 55833 |
rs796911908 | snp | A/G | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34027642 | GCAGGCGAGTCATGA[A/G]GTCAAGAGATCGAGA | 55833 |
rs796952823 | in-del | -/G | | | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935164 | GCTGTTGGAAGTGGC[-/G]GGGGGGGGGGGTCTC | 55833 |
rs796957938 | in-del | -/AA | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34017018 | AAAAGAAAAAAAAGG[-/AA]AAAAAAAAAAAGAGT | 55833 |
rs796983789 | in-del | -/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:33970438 | TGTTTGTGTGCATTA[-/T]TTTTTTTTTTCAGGC | 55833 |
rs797014189 | in-del | -/A | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34041299 | CTCTACTAAAAATGC[-/A]AAAAAAAAAAAAAAA | 55833 |