SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs715737 | snp | A/G | 0.139225 | 0.224118 | intron-variant | UBAP2L | GRCh38.p7 | 1:154264094 | CATAGTCAAGGAGAT[A/G]TCTGACCAAACCGCT | 9898 |
rs1044013 | snp | A/G | 0.499767 | 0.0107802 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | HAX1, UBAP2L | GRCh38.p7 | 1:154270639 | GTTGGGCTGATATAT[A/G]TTTGGGGGTCCCACC | 9898 |
rs1044015 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | HAX1, UBAP2L | GRCh38.p7 | 1:154270671 | GCCCTAAGTCTCCTT[C/T]TTTATTATTAGGAAA | 9898 |
rs1194580 | snp | A/C | 0.35207 | 0.228214 | intron-variant | UBAP2L | GRCh38.p7 | 1:154247009 | TGATTCCTTTGATGT[A/C]GTTAATGACCTTGGA | 9898 |
rs1194581 | snp | A/G | 0.140919 | 0.224948 | intron-variant | UBAP2L | GRCh38.p7 | 1:154243605 | ggcgtggtggcacac[A/G]cctgtaatcccagct | 9898 |
rs1194582 | snp | C/T | 0.351853 | 0.228311 | intron-variant | UBAP2L | GRCh38.p7 | 1:154243497 | CTCCAGCCTGGCCGA[C/T]ACAGTGAGACTCTGT | 9898 |
rs1194595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAP2L | GRCh38.p7 | 1:154267944 | ccagatcgcaccatt[A/G]cactccagcctgggc | 9898 |
rs1194596 | snp | A/G | 0.499885 | 0.00758699 | intron-variant | UBAP2L | GRCh38.p7 | 1:154265907 | TGATCTTGATACTAG[A/G]CCTTTACATCTTAAG | 9898 |
rs1194597 | snp | A/G | 0.105569 | 0.204058 | intron-variant | UBAP2L | GRCh38.p7 | 1:154265012 | GTAAAAGAAGGGAAC[A/G]ATACAGGAGTATCTT | 9898 |
rs1194599 | snp | A/C | 0.352504 | 0.228019 | downstream-variant-500B, intron-variant | UBAP2L | GRCh38.p7 | 1:154263976 | ACTCAGGCTCTGTGG[A/C]GACTGTGCTATCCTG | 9898 |
rs1194600 | snp | C/G | 0.352721 | 0.227922 | downstream-variant-500B, intron-variant | UBAP2L | GRCh38.p7 | 1:154263533 | GGTTCCTAGTGTCCA[C/G]AAAGACATGCACGGA | 9898 |
rs1194601 | snp | A/T | 0.102726 | 0.202016 | intron-variant | UBAP2L | GRCh38.p7 | 1:154260442 | CTGTGAGTAGTAGCA[A/T]AAAGGGGCAGAGATG | 9898 |
rs1194602 | snp | A/G | 0.338976 | 0.23363 | intron-variant | UBAP2L | GRCh38.p7 | 1:154259467 | CGGCGGCTCATGCCT[A/G]TAAGCTCAGCACTTA | 9898 |
rs1194603 | snp | C/T | 0.350109 | 0.229081 | intron-variant | UBAP2L | GRCh38.p7 | 1:154255811 | TTAGAACTGTCCAAC[C/T]GTAAGATTGTCCCAA | 9898 |
rs1194604 | snp | A/C | 0.403861 | 0.228621 | intron-variant | UBAP2L | GRCh38.p7 | 1:154254763 | ACCAAAATAAAGCTG[A/C]ATCAGTGCTAACTTT | 9898 |
rs1194605 | snp | G/T | 0.0370281 | 0.130931 | intron-variant | UBAP2L | GRCh38.p7 | 1:154254105 | ACCAATTCCCAAGGG[G/T]TCATGAAGCCACTAC | 9898 |
rs1205590 | snp | A/G/T | 0.109883 | 0.20728 | intron-variant | UBAP2L | GRCh38.p7 | 1:154266429 | TCCTGAGATGAGGTG[A/G/T]TATCTGTAGCCTTTC | 9898 |
rs1212352 | snp | A/T | 0.466412 | 0.125164 | intron-variant | UBAP2L | GRCh38.p7 | 1:154266807 | AAATTACATGACACG[A/T]TAAACAATTTGCCAC | 9898 |
rs1212762 | snp | A/G | 0 | 0 | intron-variant | UBAP2L | GRCh38.p7 | 1:154254900 | GGGGAAAAGCCTGAA[A/G]AACACTCACCTTCAA | 9898 |
rs1488085 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAP2L | GRCh38.p7 | 1:154269873 | TGGGTGATCACAAGG[C/T]AATTTCATTTCCATT | 9898 |
rs1619529 | snp | A/C/G | 0 | 0 | synonymous-codon | UBAP2L | GRCh38.p7 | 1:154258979 | CTGTATCTTTCAGCC[A/C/G]CAAGTATATGGTTAT | 9898 |
rs1621773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAP2L | GRCh38.p7 | 1:154250163 | gctcaggtgggagga[C/T]tgcttgagcccagga | 9898 |
rs1685614 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | HAX1, UBAP2L | GRCh38.p7 | 1:154271954 | TTGGGGGGTTATAAA[A/G]AAAAACCCCCCGGGG | 9898 |
rs1760791 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | UBAP2L | GRCh38.p7 | 1:154249801 | CAATTAGCTGAGTGC[A/G]GTGGTGTGCACCTGT | 9898 |
rs1803502 | snp | A/T | | | utr-variant-3-prime, intron-variant | UBAP2L | GRCh38.p7 | 1:154263446 | TGGAAGGCATGTAGT[A/T]TCAACTTGTAACAAA | 9898 |
rs1986709 | snp | C/T | 0.499 | 0.0223418 | intron-variant | UBAP2L | GRCh38.p7 | 1:154252036 | TGGAATGCAGTGGTG[C/T]GATCTCGGCTTACTG | 9898 |
rs2220390 | snp | C/T | 0.409382 | 0.192607 | intron-variant | UBAP2L | GRCh38.p7 | 1:154260540 | GGACTTGAAGGACAA[C/T]GATGGATCAGGGAAA | 9898 |
rs2274989 | snp | A/G | 0.00275043 | 0.0369818 | intron-variant | UBAP2L | GRCh38.p7 | 1:154251436 | TTTAGTCTTTAGTAA[A/G]GTTGTATTAAAGCCA | 9898 |
rs2274990 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBAP2L | GRCh38.p7 | 1:154258899 | TGAATGTTCTGTTGA[A/G]TTAGCTTGTCTCTTG | 9898 |
rs2274991 | snp | C/T | 0 | 0 | intron-variant | UBAP2L | GRCh38.p7 | 1:154259922 | AGTGACATTGAATCT[C/T]TGCTCTTTTTTCCCC | 9898 |
rs2274992 | snp | C/T | 0.0025618 | 0.0356979 | synonymous-codon, utr-variant-5-prime | UBAP2L | GRCh38.p7 | 1:154237135 | AAATGGTCACTCACT[C/T]GTCCCATCATCTGGT | 9898 |
rs2274993 | snp | A/G | 0.221121 | 0.248326 | intron-variant | UBAP2L | GRCh38.p7 | 1:154237014 | AAGGTTCTGGAAAAA[A/G]TAAAACTTAAGAGTC | 9898 |
rs2282227 | snp | A/G | 0.329317 | 0.237084 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | HAX1, UBAP2L | GRCh38.p7 | 1:154270621 | GTACGGATGAGGCGG[A/G]GAGGTGGGACCCCCA | 9898 |
rs2307621 | in-del | -/AT | 0.499902 | 0.00698814 | intron-variant | UBAP2L | GRCh38.p7 | 1:154265789 | GAACACAAAAACCAC[-/AT]GTCATTTTCAGTATA | 9898 |
rs2340473 | snp | C/T | 0.498964 | 0.02274 | intron-variant | UBAP2L | GRCh38.p7 | 1:154252868 | CCGGCCCAAATCTTA[C/T]ATGGTTCTTGAGGGA | 9898 |
rs2483709 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | UBAP2L | GRCh38.p7 | 1:154241215 | TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA | 9898 |
rs2633434 | snp | C/T | 0.131381 | 0.220067 | intron-variant | UBAP2L | GRCh38.p7 | 1:154250482 | CCAAGTTTAAAGTAc[C/T]gcaagttctcattta | 9898 |
rs2879788 | snp | A/T | 0.498964 | 0.02274 | intron-variant | UBAP2L | GRCh38.p7 | 1:154231834 | ATCTGGAAGTTGTAG[A/T]CATAATACTTGATAC | 9898 |
rs3203752 | snp | C/T | | | missense | UBAP2L | GRCh38.p7 | 1:154261682 | AGTGGATATGGGTCT[C/T]ATGGATACAACACTG | 9898 |
rs3211038 | snp | C/T | 0 | 0 | synonymous-codon | UBAP2L | GRCh38.p7 | 1:154261657 | ATCGGCCACCCCTTT[C/T]CAACAGCCGAGTGGA | 9898 |
rs3211039 | snp | A/G/T | 1.6473e-05 | 0.00286988 | missense | UBAP2L | GRCh38.p7 | 1:154261674 | AACAGCCGAGTGGAT[A/G/T]TGGGTCTCATGGATA | 9898 |
rs3762339 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | UBAP2L | GRCh38.p7 | 1:154236401 | ATAGGGTTTTGCTCT[A/G]TTGCCTAGGCTGGTC | 9898 |
rs3762340 | snp | A/T | 0.236144 | 0.249616 | intron-variant | UBAP2L | GRCh38.p7 | 1:154236693 | AAAATGATCAGAATG[A/T]TTTCTAGACTGGTCA | 9898 |
rs3790613 | snp | A/C | 0.248471 | 0.249995 | intron-variant | UBAP2L | GRCh38.p7 | 1:154238195 | TTGTTCGCCAAGTTG[A/C]TATCTTATAAATTCA | 9898 |
rs3790614 | snp | A/G | 0.247905 | 0.249991 | intron-variant | UBAP2L | GRCh38.p7 | 1:154260292 | GTGGGAGAATTGCTT[A/G]AGCCCAGGAGTTCAA | 9898 |
rs3811453 | snp | C/T | 0.237593 | 0.249692 | upstream-variant-2KB, intron-variant | C1orf43, UBAP2L | GRCh38.p7 | 1:154222103 | AGGCAAAAACGTTAA[C/T]AATAATAACAAAAAC | 9898 |
rs3828076 | snp | A/G | 0.4444 | 0.15719 | intron-variant | UBAP2L | GRCh38.p7 | 1:154238226 | TTTTTAACACATTTC[A/G]TGGGTGGAGGCTGAA | 9898 |
rs3828077 | snp | A/G | 0.248188 | 0.249993 | intron-variant | UBAP2L | GRCh38.p7 | 1:154260134 | TAAATCAGGATTGGT[A/G]GATTCAAAATCCTGC | 9898 |
rs3838414 | in-del | -/GTCA | | | intron-variant | UBAP2L | GRCh38.p7 | 1:154246167 | ATGTTAGCGTGTTCA[-/GTCA]TTCTTCATGAAGATC | 9898 |
rs4040743 | in-del | -/TCAG | 0.499247 | 0.019385 | intron-variant | UBAP2L | GRCh38.p7 | 1:154246164 | GGAATGTTAGCGTGT[-/TCAG]TCATTCTTCATGAAG | 9898 |
rs4240871 | snp | A/G | 0.498982 | 0.0225409 | intron-variant | UBAP2L | GRCh38.p7 | 1:154230259 | CAATCCTCCTGCCTC[A/G]GCCTTCCAAAATGTT | 9898 |
rs4393149 | snp | A/G | 0.353803 | 0.227431 | intron-variant, upstream-variant-2KB | UBAP2L | GRCh38.p7 | 1:154223277 | AGTATATGCAATAGT[A/G]TATAGCTAGTCATGC | 9898 |
rs4406621 | snp | A/G | 0.139903 | 0.224452 | intron-variant | UBAP2L | GRCh38.p7 | 1:154235571 | ctggagtgcagtggc[A/G]cgatcttggctcact | 9898 |
rs4845365 | snp | C/T | 0 | 0 | intron-variant | UBAP2L | GRCh38.p7 | 1:154227067 | ACATCAGGTGATCTG[C/T]CTGCCTTGGGCTCCC | 9898 |
rs4845610 | snp | C/T | 0.349671 | 0.229272 | intron-variant | UBAP2L | GRCh38.p7 | 1:154232952 | atcctcctgccttga[C/T]ctctcgacctcccaa | 9898 |
rs5777892 | in-del | -/T | 0.354881 | 0.226936 | intron-variant, upstream-variant-2KB | UBAP2L | GRCh38.p7 | 1:154223524 | GTACTTGGTTAAACA[-/T]TTTTTTTTTTTGTAA | 9898 |
rs5777894 | in-del | -/T | 0.359575 | 0.224707 | intron-variant | UBAP2L | GRCh38.p7 | 1:154231289 | GCCACCACACTTGGC[-/T]TTTTTTTTTTTTTCT | 9898 |
rs6427509 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBAP2L | GRCh38.p7 | 1:154247242 | TACTAATTCAGAACT[C/T]GGTCAGTTTTTAATT | 9898 |
rs6657214 | snp | C/T | 0.498945 | 0.022939 | intron-variant | UBAP2L | GRCh38.p7 | 1:154234062 | GGGCTTGGTGGCTCA[C/T]GTCTGTAATCCCAGC | 9898 |
rs6664963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAP2L | GRCh38.p7 | 1:154240472 | CTGTGCCATGACCAT[A/G]GCAGGTCAGGTTTCA | 9898 |
rs6673752 | snp | C/G | 0.247905 | 0.249991 | intron-variant | UBAP2L | GRCh38.p7 | 1:154246701 | TTTAATCCTTTTGCA[C/G]CCCTCATTAAACTAT | 9898 |
rs7516809 | snp | C/T | 0.352287 | 0.228117 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233025 | Ctttttttctttttt[C/T]tttttttgagatgga | 9898 |
rs7517578 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | UBAP2L | GRCh38.p7 | 1:154248748 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 9898 |
rs7524346 | snp | A/C | 0.499831 | 0.00918375 | intron-variant | UBAP2L | GRCh38.p7 | 1:154248617 | GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAC | 9898 |
rs7525244 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-3-prime, downstream-variant-500B | HAX1, UBAP2L | GRCh38.p7 | 1:154270769 | AAGTGGttttttttt[G/T]gtttttttttttttt | 9898 |
rs7526644 | snp | C/T | 0.381503 | 0.21262 | intron-variant | UBAP2L | GRCh38.p7 | 1:154236277 | GGTCTTAGCTCACTG[C/T]AGCCTCTGCCTCCTG | 9898 |
rs7533952 | snp | C/T | 0.351853 | 0.228311 | intron-variant | UBAP2L | GRCh38.p7 | 1:154248740 | AGAATGGTGTGAACC[C/T]GGGAGGCGGAGCTTG | 9898 |
rs7542875 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | UBAP2L | GRCh38.p7 | 1:154223949 | GCAGAAAAGTATAAA[C/T]TTACCCTCTTTGGAA | 9898 |
rs7542975 | snp | A/G | 0.352504 | 0.228019 | intron-variant | UBAP2L | GRCh38.p7 | 1:154232337 | CCAAAAAAAAAAAAA[A/G]GAAAGAAATCTGATA | 9898 |
rs7554027 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-3-prime, downstream-variant-500B | HAX1, UBAP2L | GRCh38.p7 | 1:154270770 | AGTGGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 9898 |
rs7554731 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233116 | actcctgggttcaag[C/T]gattctcctgcccca | 9898 |
rs9803857 | snp | A/G | 0.499801 | 0.00998203 | intron-variant, upstream-variant-2KB | C1orf43, UBAP2L | GRCh38.p7 | 1:154219315 | AAGACAGTCACCTAA[A/G]GAGAAAGTACAGACA | 9898 |
rs9803862 | snp | A/G | 0.446118 | 0.155041 | intron-variant, upstream-variant-2KB | C1orf43, UBAP2L | GRCh38.p7 | 1:154219667 | CCACAGCACTGAGCA[A/G]GTAAGCCAAGTTCCA | 9898 |
rs9804042 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | C1orf43, UBAP2L | GRCh38.p7 | 1:154219165 | taattctgattcaca[A/T]atgttgggtttgaga | 9898 |
rs9804045 | snp | A/G | 0.353154 | 0.227726 | intron-variant, upstream-variant-2KB | C1orf43, UBAP2L | GRCh38.p7 | 1:154219215 | TGGAAATGTCAGGTA[A/G]TCAGTTGGCAATATA | 9898 |
rs9943093 | snp | C/G | 0.499839 | 0.00898417 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233080 | gtgcaatggcaggat[C/G]tcagcttactgcaac | 9898 |
rs9943097 | snp | C/T | 0.351853 | 0.228311 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233347 | TTCTTTGAGATGGAA[C/T]CTTGCTCTGTGGCCC | 9898 |
rs10158820 | snp | C/T | 0.499631 | 0.0135733 | intron-variant | UBAP2L | GRCh38.p7 | 1:154245287 | CCCCACCCTGGGCTA[C/T]CTCATTAGCATTCAG | 9898 |
rs10797058 | snp | C/T | 0.352504 | 0.228019 | intron-variant | UBAP2L | GRCh38.p7 | 1:154228228 | AGTCTTGCTCTGTGG[C/T]CCAGGCTAGAGTGCA | 9898 |
rs10797061 | snp | C/T | 0.365853 | 0.221536 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233736 | GGTGAGATTAGAGAA[C/T]GTGCCCAAGAGTAGA | 9898 |
rs10797067 | snp | G/T | 0.476487 | 0.105846 | intron-variant | UBAP2L | GRCh38.p7 | 1:154265162 | TTAGGATGTTGGGAA[G/T]GTTTTCCAGATTAAG | 9898 |
rs11265310 | snp | C/T | 0.180702 | 0.240204 | intron-variant, upstream-variant-2KB | UBAP2L | GRCh38.p7 | 1:154224650 | TGTTTTCTTAGGTGA[C/T]TGAATACAGTATTTA | 9898 |
rs11265353 | snp | A/C | 0.444267 | 0.157354 | intron-variant | UBAP2L | GRCh38.p7 | 1:154238739 | ATTAATTTTTTTTTT[A/C]TTTTCTTTTTTTCTT | 9898 |
rs11265398 | snp | C/T | 0.154903 | 0.231207 | utr-variant-3-prime, intron-variant | UBAP2L | GRCh38.p7 | 1:154263181 | ATTTATACACACACA[C/T]AAAACACAGCCCCCA | 9898 |
rs11301778 | in-del | -/T | 0.35207 | 0.228214 | intron-variant | UBAP2L | GRCh38.p7 | 1:154246075 | TAAGCATTTCAAGGC[-/T]TTTGTGTTTGAACCC | 9898 |
rs11412846 | in-del | -/T | 0.615018 | 0.125161 | intron-variant | UBAP2L | GRCh38.p7 | 1:154254816 | GTTTTTTTTTTTTTT[-/T]ACCAGAATGGCTTCA | 9898 |
rs11422922 | in-del | -/TT | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-3-prime, downstream-variant-500B | HAX1, UBAP2L | GRCh38.p7 | 1:154270786 | TTTTTTTTTTTTTTT[-/TT]GTACTGTGTCCTCAA | 9898 |
rs11590537 | snp | A/G | | | intron-variant | UBAP2L | GRCh38.p7 | 1:154225956 | gtagctgggattaca[A/G]gagtgtgctaccatg | 9898 |
rs11808153 | snp | C/T | 0.081446 | 0.184634 | intron-variant | UBAP2L | GRCh38.p7 | 1:154265587 | CCTATCTTCTTGACC[C/T]GATGCCTTATACCCC | 9898 |
rs12023901 | snp | G/T | 0.199393 | 0.24484 | intron-variant | UBAP2L | GRCh38.p7 | 1:154235159 | TGGTTTGGTTTTTTT[G/T]TTGTTGTTGTTGTTT | 9898 |
rs12025237 | snp | A/C | 0.248471 | 0.249995 | intron-variant | UBAP2L | GRCh38.p7 | 1:154232644 | TGGAAGGCTTTGTAT[A/C]ATCAGTATCTCTTGG | 9898 |
rs12026615 | snp | C/T | 0.248188 | 0.249993 | intron-variant | UBAP2L | GRCh38.p7 | 1:154237734 | TTTCTGGTGCCCTGT[C/T]GAACAGCCTTCTTGG | 9898 |
rs12027999 | snp | C/T | 0.248471 | 0.249995 | intron-variant | UBAP2L | GRCh38.p7 | 1:154233882 | AGTTTTTTCTTTTTT[C/T]TTTTTAGCCCAGGAA | 9898 |
rs12028554 | snp | A/G | 0.498813 | 0.0243321 | intron-variant | UBAP2L | GRCh38.p7 | 1:154250625 | TCGAGAAGCCGAGGC[A/G]GACGGATCACTTGAG | 9898 |
rs12049162 | snp | A/G | | | intron-variant | UBAP2L | GRCh38.p7 | 1:154232279 | cagtgagccgagatc[A/G]caccactgcactcca | 9898 |
rs12062977 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBAP2L | GRCh38.p7 | 1:154239040 | GCCACCACGCCTGGT[C/T]GTTGTTAATTTCATG | 9898 |
rs12087877 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | C1orf43, UBAP2L | GRCh38.p7 | 1:154220133 | AGGCGTGGGGTCTGT[C/G]CTCTAGCGTTAAAGG | 9898 |
rs12145394 | snp | C/T | 0.200492 | 0.245049 | intron-variant | UBAP2L | GRCh38.p7 | 1:154229179 | CCTCAATATCAGCTT[C/T]GCATTGCACACTACT | 9898 |
rs12354278 | snp | A/T | 0.123798 | 0.215808 | upstream-variant-2KB, utr-variant-3-prime, intron-variant, downstream-variant-500B | HAX1, UBAP2L | GRCh38.p7 | 1:154270981 | GTGGAATAAAATGAA[A/T]TCTTCGCCCTTTAAG | 9898 |
rs12566324 | snp | C/T | 0 | 0 | intron-variant | UBAP2L | GRCh38.p7 | 1:154267802 | gcccagccTGGAGTT[C/T]TAAGTTCGGATTTCA | 9898 |