SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs139675297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129572 | TGTAGGCGGAGGTAA[C/T]GTGTCTGGGAGGCTC | 10277 |
rs139676749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112665 | TCAGCCTCCCAAAGT[A/G]TAGAAATATTTCTCC | 10277 |
rs139683709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10048758 | TGCTGACTGGAGCAA[A/G]TTCAAGAGAGAATGG | 10277 |
rs139707942 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | UBE4B | GRCh38.p7 | 1:10167624 | TTTGAGACGGAGTCT[C/G]ACTCTGTCACTAGGC | 10277 |
rs139720343 | snp | A/G | 6.68338e-05 | 0.00578035 | intron-variant | UBE4B | GRCh38.p7 | 1:10179844 | AAGCATCCTCTCTCA[A/G]GAAGAGCCCTCCCAT | 10277 |
rs139731247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058145 | TGCTTGGGTAAAAGC[A/G]CTAGATACTTTAGGG | 10277 |
rs139737735 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100700 | GCTGGGATTACAGGC[A/G]TGTGCCACCACGCCT | 10277 |
rs139760788 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060078 | CAGTCGTCAGGTCCC[-/TG]TGTGTGTGTGGAGGG | 10277 |
rs139770914 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | UBE4B | GRCh38.p7 | 1:10066824 | GACAGGAGAATGGCA[G/T]GAACCCGGGAGGCAG | 10277 |
rs139775644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154490 | GAAATAATTACGAAT[A/G]TTTGTAAGTGATGTT | 10277 |
rs139852529 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10058390 | TAACATTTCTCTATT[A/G]CTTGGAAGCCTTGGT | 10277 |
rs139871424 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10142586 | TGAGGCAGGAGAATC[G/T]CTTGAACACGGGAGA | 10277 |
rs139915809 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE4B | GRCh38.p7 | 1:10174373 | ATTCCAGCCTGGGTG[A/G]CAGAGCAAGACTCCA | 10277 |
rs139942341 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10128746 | TCTAGAGCTGCGTCC[A/G]AATCACAGAGGAAAT | 10277 |
rs139993738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178979 | TATTTTTAGCTCATA[G/T]TGTAAATTGAGAGGA | 10277 |
rs140009702 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10108161 | GGTGTGTGTGTGTGT[G/T]TGTGTGCGTGCGTGC | 10277 |
rs140051271 | snp | A/G | 4.95372e-05 | 0.00497656 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132450 | TACATGGCGGCTGTC[A/G]TCAATGCCAATATGA | 10277 |
rs140083532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159091 | TTTTGGTGTTTTCTA[C/T]GATGACAGTGTTAAA | 10277 |
rs140106997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171427 | TGTAAATGAAGATGA[A/G]TGGGTTGTTTTCCTT | 10277 |
rs140137914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064568 | CCAGGTGCTGCCAGG[G/T]CTTCCTGTGTCTGCA | 10277 |
rs140149592 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10067159 | TGCCTGCAATCACAA[C/T]GGCCTTCACTGTTTT | 10277 |
rs140154432 | snp | C/T | 0.00179399 | 0.0298961 | intron-variant | UBE4B | GRCh38.p7 | 1:10144899 | TGGGTAAGATGGATC[C/T]GGCTGTTTTCTTTCA | 10277 |
rs140191968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10099112 | CCGGGCATGGTGGTG[C/T]GTGCCTGTAATCCCA | 10277 |
rs140202311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173968 | CCTCTGGTGGCACCT[A/G]GCTTGGGTTGTAGAC | 10277 |
rs140216492 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100286 | GAGCCATCGTGCCTG[A/G]CCTATTTTCTCAATT | 10277 |
rs140232669 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151478 | CTGCTGTTCAGCCAC[A/G]AACCCAGAAGTTTTT | 10277 |
rs140250872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096419 | GCCTCGGTTTGTGTC[A/T]GTGGGCTAAACAGAT | 10277 |
rs140250968 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10142628 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC | 10277 |
rs140291546 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10104335 | TTTCTTTACAGTAGT[A/C]ATTTGGAACGCAGAA | 10277 |
rs140340507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073886 | CATGCTCACTCTCTC[A/G]GCTAGTGGCCTGGCT | 10277 |
rs140360856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039275 | AAAAGTGATACTTAA[C/T]GCTGAGTAGCAGTTG | 10277 |
rs140394892 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10138710 | TAACCTTGAAATTTC[C/T]ATCTTGTTTCAGTTG | 10277 |
rs140397347 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10109444 | TCCTTAATTACAAAA[C/T]GCCATCCCAGTCAGT | 10277 |
rs140502312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074876 | CATTTGATGATTCCT[A/C]AGCTTTTATCTCCAA | 10277 |
rs140537505 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10125961 | GTTGATTGTTGGCCT[G/T]TTTATCTTGTTTTCC | 10277 |
rs140545247 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | UBE4B | GRCh38.p7 | 1:10116936 | GTTTTTATGTCGATA[A/G]CAAATATGTTCATGT | 10277 |
rs140572802 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10059665 | CCGAGGCGTGAAGGG[C/T]GGCAGCCGATCCCTA | 10277 |
rs140612245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079045 | GCTGGTTTTGAACTC[C/T]TGGCCTCAAGCGATC | 10277 |
rs140614980 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10119276 | CCGCGCCTGGCCTCT[A/G]AGGTTCTTAAGTATA | 10277 |
rs140659705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164312 | TGCCACTACATTTCA[C/T]ATTTCAGCCTGGGCA | 10277 |
rs140713896 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10156310 | AGTGGTACAATTACA[G/T]CACCATGCACTCTTG | 10277 |
rs140736060 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10104896 | TTTCCATGAGTTAAA[A/G]CTTTTGTTTAGTGGT | 10277 |
rs140758516 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10142123 | ATCACCAGGGATCAT[G/T]TATATAGCTGTTTTT | 10277 |
rs140760739 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094078 | CAAATGCCTGGGTAA[A/C]CATTCTTCTTTTTTC | 10277 |
rs140763917 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10060703 | CACCTTGACTTCTAA[C/T]GGTAGAGGTTCATTT | 10277 |
rs140772149 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UBE4B | GRCh38.p7 | 1:10138060 | CTGCTTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10277 |
rs140835639 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10176710 | AGCAATGTCTATTCA[A/T]GTTCTTTGCCCATTT | 10277 |
rs140883136 | snp | C/T | 0.000115654 | 0.00760352 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179947 | AGAGAAACAGAACAG[C/T]GATCACTAAACCGTT | 10277 |
rs140906123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063961 | TATTCCCCTGCTTAA[A/C]TCCTTCAAAAGATGT | 10277 |
rs140977077 | snp | C/T | 6.58957e-05 | 0.00573964 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151410 | CAACCAGAACTACAT[C/T]CGAAACCCATATTTG | 10277 |
rs140997057 | in-del | -/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032944 | CCCCGCCTCCCTGAC[-/G]GGGGTCACGTGATCC | 10277 |
rs141018701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160835 | GTAGTTCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 10277 |
rs141028646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10136378 | AGGAGACTGAGGCAG[A/G]AGGATTGCCTGAGCC | 10277 |
rs141037031 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10054719 | TCTAGCCATGGTAAC[A/C]CTTGCGGGGCATTTT | 10277 |
rs141070462 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100068 | AGTCTTGGCTCACTG[C/T]GAGCTCTGCCTCCCG | 10277 |
rs141091703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10121796 | AAAGACCAAAAAGTG[A/G]TTACTATTGGTAAGA | 10277 |
rs141110713 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10175287 | GACTGCATATCTGTC[A/G]TCCATGAAGCATTGT | 10277 |
rs141124105 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10133744 | AATGAGACCCCATCT[C/G]TACAAAATATACAAA | 10277 |
rs141125743 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10131538 | AACTAAGGTAATTTT[A/G]ATCATGGGAAAGAAG | 10277 |
rs141133286 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10050532 | TCTCTCCTAACATTA[A/G]CCACACTGCATTGAA | 10277 |
rs141193020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155416 | CTGAAGCTTAAAAGG[A/G]TCAAGAAGCTTGCTG | 10277 |
rs141201321 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10118691 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCTCCATA | 10277 |
rs141237094 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10162254 | TCTCAGCTCACTGCA[A/G]TCTTTGCCTCCTGGG | 10277 |
rs141301368 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033313 | ATCACGAAGAAACAG[C/T]AGGCTCGGGGCACGA | 10277 |
rs141368455 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10146562 | GAATTCCATCCTTAG[C/T]GGCCAGCATTTTGCC | 10277 |
rs141383181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069791 | CCACCGCCTCGGACT[A/C]CCCTCGGCCGATGAT | 10277 |
rs141422686 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10144325 | GAGACTTCTTTTTTT[C/T]CCTCCCAGAAAAATA | 10277 |
rs141429821 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10065891 | AAAATAAATGGAATC[A/G]TTATGTGTACCCTTT | 10277 |
rs141450760 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090793 | AGAAGCCTATGCATT[-/TG]TGTGTGTGTGTGTGT | 10277 |
rs141539126 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073175 | GGTAGGATTGATGGG[A/T]TCAGGATTCCAAATG | 10277 |
rs141557548 | in-del | -/ATA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152294 | ATAATAATAATAATA[-/ATA]CCACTTTTCACCTGT | 10277 |
rs141566548 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044081 | CTTGCTCTGTTACTC[-/A]ACGCTGGAGTGCAGT | 10277 |
rs141611024 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077346 | TCTGTGTCCAAATTT[-/C]CCCTCTTATGACAGC | 10277 |
rs141613487 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10091589 | AGCTAAGATTACAGG[C/T]GCATGCCACCATGCC | 10277 |
rs141678599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10077009 | CTCAGCCTCCCAAAG[C/T]GTTGGGATTACAGGT | 10277 |
rs141685825 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10046118 | AGGGGAGGGGAGGTC[A/G]TGTGCCTCTTCATGG | 10277 |
rs141697170 | snp | C/T | 5.59895e-05 | 0.00529071 | intron-variant | UBE4B | GRCh38.p7 | 1:10134968 | TGTTTAAAAATACTT[C/T]TTCTTTTCAACTTTC | 10277 |
rs141697597 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10086184 | CACCGTGTTAGCCAG[C/G]ATGGTCTCGATCTCC | 10277 |
rs141707832 | snp | C/G/T | 6.59287e-05 | 0.00574113 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130807 | GCATTACTTAGAGCT[C/G/T]GGAAGGGTAAGTGTT | 10277 |
rs141713886 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10127826 | AAATAAGAGCTACAG[C/T]GCAACAGTTGAACAG | 10277 |
rs141714083 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | UBE4B | GRCh38.p7 | 1:10044809 | GCTGTTCTTGAACTC[C/T]TGAGCTCAAGCAGTC | 10277 |
rs141721679 | snp | C/T | 0.031825 | 0.122064 | intron-variant | UBE4B | GRCh38.p7 | 1:10097199 | GGAAATTACCCAGAA[C/T]GTACCACAAAGAACA | 10277 |
rs141750784 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137192 | AGACTCCGGGCTATC[C/T]GGGAGCTCAATAGGT | 10277 |
rs141765280 | snp | A/T | 1.79586e-05 | 0.0029965 | intron-variant | UBE4B | GRCh38.p7 | 1:10132529 | TGTCAAATTCATTCA[A/T]CTGACCCAGATTTAG | 10277 |
rs141780625 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10090344 | AGGCTGGTCTTGAAT[G/T]CCTGGACTGAAGCGA | 10277 |
rs141788988 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10163607 | CGGGAGGCGGAGGTT[A/G]CAGTGAGCCAAGATC | 10277 |
rs141843802 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10092667 | ACCCCATCTCTACTA[A/G]AAGTACAAAAATTAG | 10277 |
rs141859404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10049244 | TGTGGAGATGCTGCT[C/T]GAATATGACGAAGAC | 10277 |
rs141859758 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10107798 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 10277 |
rs141945015 | in-del | -/GT/GTGT | 0.286187 | 0.254868 | intron-variant | UBE4B | GRCh38.p7 | 1:10101976 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATTAATATAGATAAT | 10277 |
rs141992045 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | UBE4B | GRCh38.p7 | 1:10035013 | TTTGTTTGTTTGTTT[G/T]TTTGAGACGGAGTCT | 10277 |
rs142009872 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062564 | GAGGTCTGCCCACCT[G/T]GGCTCCCAAAGTGTT | 10277 |
rs142071435 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10109131 | ATTGTGCGCCAGATG[C/T]GGTGTCAGCTCTGTC | 10277 |
rs142086424 | in-del | -/AAAC | 0.187369 | 0.242028 | intron-variant | UBE4B | GRCh38.p7 | 1:10039094 | AACACACACACAGAA[-/AAAC]AAACAAAAAAGCAAT | 10277 |
rs142095509 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10108205 | CCTCCCAGCCTCCAC[C/T]GCCCCCCTGTTCACC | 10277 |
rs142096652 | snp | A/C/G/T | 0.000296783 | 0.0121785 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126871 | CTACTTTAAATACCC[A/C/G/T]CTCATGGTAAAACTT | 10277 |
rs142097597 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10153023 | TTGCTAGCTCTGGGG[A/G]TACGAGACAAAGCTG | 10277 |
rs142137203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065018 | ATCCACCCGCCTGGC[C/T]TCCCAAAGTGCTGGG | 10277 |
rs142137213 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10115629 | CAAAGTCTAAGGACA[A/G]TGATGTCCATACAGA | 10277 |
rs142162753 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10148911 | CACCACTGCACTCCA[A/G]CCTGGGTGACAGAGT | 10277 |
rs142200548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110835 | ACATAGAAACAGTGG[A/G]AAAGAAATCATTCTG | 10277 |
rs142219487 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10123528 | GAATACTTTTCCTAT[C/T]CAAGAAGATACCATT | 10277 |
rs142247248 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10053024 | GGTCATCAGGGGTTC[C/T]GCCCTCAGGACCTCA | 10277 |
rs142251510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132878 | CGAAGCAGCTTTGGT[A/T]CAAGCCCAGCACGCA | 10277 |
rs142278958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069509 | AGGGTGGTGGTTTTC[C/T]CACAACCCTGTAAGG | 10277 |
rs142379873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10059303 | TATACAGCAACAGCA[A/G]CAAGGATTGCTGGTG | 10277 |
rs142380751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056048 | ACCATCCACTTCTAT[C/G]CCCTGGGATGTTTTT | 10277 |
rs142519801 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10068242 | GTATGCTGGCCAGGC[C/T]GGTCTCAAACTCCTG | 10277 |
rs142522772 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10146076 | CTAGACTTCTTCAAG[A/G]TGCACAATTAACAAG | 10277 |
rs142566274 | snp | A/G | 6.63978e-05 | 0.00576146 | intron-variant | UBE4B | GRCh38.p7 | 1:10130855 | GGAAGTATCAAAGAT[A/G]AGCTCCAGATACAGA | 10277 |
rs142599147 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093627 | AAGGGTTAAAATTGT[A/C]TTTATTCAGTGATTG | 10277 |
rs142657729 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | UBE4B | GRCh38.p7 | 1:10131895 | GAGGCGGAGGTTGCA[C/G]TGAGCCGAGATGTGC | 10277 |
rs142660803 | in-del | -/GTATTTATGTAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071679 | ACATACAGTATATAC[-/GTATTTATGTAT]GTATTTATGTATGTA | 10277 |
rs142671692 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10080890 | AGACAGTAGATGGTG[A/G]TTACCAGAGGCTGGG | 10277 |
rs142673569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10051235 | ACTTAATCTTTCTGA[A/G]CCTCAGTTTCCTCAC | 10277 |
rs142674147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10156957 | GAGGATCGCTTGAGG[C/T]AGGAATTTGAAACCA | 10277 |
rs142686814 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10081808 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10277 |
rs142704128 | snp | A/C/T | 0.00013179 | 0.0081166 | synonymous-codon, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130512 | TAGGTTGCTTCTTTG[A/C/T]GGTTGTGGTTGCCGA | 10277 |
rs142746106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085666 | AGGTTTTTTTTTAAC[A/G]TCAGTTCTATCATTT | 10277 |
rs142747109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037176 | GGAATTACAGGCATG[C/T]GCCACCATACCCGGC | 10277 |
rs142747642 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093851 | AGGAGTGGGCCACCA[C/T]GCCCAGCTAATTTTT | 10277 |
rs142750891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161065 | AGTCTGGGTGGAGGT[A/G]CTTGTTCCCTGGGAT | 10277 |
rs142791718 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10075275 | CCTGTGGACTAGAGC[A/T]TGCTTGGCCCTGCTC | 10277 |
rs142863080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155248 | CTTTGCCATGTGTGC[C/T]CTCTGGCCTGGACCA | 10277 |
rs142864591 | in-del | -/T | 0.0528381 | 0.153711 | intron-variant | UBE4B | GRCh38.p7 | 1:10058673 | GCCGCCTGCAGGTGG[-/T]GCAAGGGTGCCTGGC | 10277 |
rs142869280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048631 | AGTATTTCATGATGT[A/G]GGGGAATGCTCAACT | 10277 |
rs142891483 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE4B | GRCh38.p7 | 1:10167269 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 10277 |
rs142901446 | snp | A/G | 0.00047763 | 0.0154463 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171272 | GTTGGACCAACTGAC[A/G]GATATTTACTTACAG | 10277 |
rs142904047 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10117877 | CTGTAGCTCGGTACC[A/G]CCAGTGACTCATATG | 10277 |
rs142905956 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10066831 | GAATGGCATGAACCC[A/G]GGAGGCAGAGGTTGC | 10277 |
rs142934066 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10142427 | CCTGTAATCCCAACA[A/C]TGGGAGGCCGAGGTG | 10277 |
rs142948257 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143409 | AGTGAGGCTCAGTCT[-/A]AAAAAAAAAGACAAC | 10277 |
rs142972445 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10113320 | ATTGGTGAGGGATCT[C/G]CCCCCATGATCCAGT | 10277 |
rs143069062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050003 | TTTGAAATTGATGAT[A/G]GAAATATGAGAACAT | 10277 |
rs143096233 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10058215 | TCTTTGGAGAAGAAA[C/T]GTGGTTAATCAATCA | 10277 |
rs143097895 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10106695 | AAATTGTTGTTTTGG[A/G]TTATTAACCTGTGTG | 10277 |
rs143101585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096075 | TGTGCGTGGCCCACT[A/G]TACTTGCATATTAAA | 10277 |
rs143104848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169817 | GTCAGGAGTTCCAGA[C/G]CAGCCTGGCCAACAT | 10277 |
rs143109491 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10177559 | TACTTGGGTGGCTAA[A/G]GTGAGAGGATTGCTT | 10277 |
rs143120602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064289 | ATTCAGTTATTACAT[G/T]AATATACAGTTAGTG | 10277 |
rs143135527 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10143072 | GAGATCGTGCCACTG[C/T]ACTCCAGGGCAACAG | 10277 |
rs143137503 | in-del | -/A | 0.121717 | 0.214577 | intron-variant | UBE4B | GRCh38.p7 | 1:10156189 | GAAGTGAATAAGAAG[-/A]AAAAAAAACTGTTGG | 10277 |
rs143140697 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032537 | GTTTTCTTTTCCCTC[A/G]CTTAGGCGGCGGGCG | 10277 |
rs143169740 | snp | C/T | 0.0554779 | 0.157039 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181536 | TCCTCAGGCCGGGCC[C/T]GGTGGCTCACGCCTG | 10277 |
rs143209769 | snp | A/G | 0.00154942 | 0.0277905 | intron-variant, synonymous-codon | UBE4B | GRCh38.p7 | 1:10101224 | GAAGCCCTTGGTACA[A/G]GTAATAGAAATAAAC | 10277 |
rs143239656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111525 | CCATGCACGCACACC[A/G]TCGTTCTTCATCCGC | 10277 |
rs143243072 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10041674 | CTTCTGAGATAGGAA[G/T]TGGAAGCCCCAGTGG | 10277 |
rs143374384 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10123273 | CGGTCTCTACTAAAA[A/G]TGCAAAAATTAACTG | 10277 |
rs143382300 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10044685 | CGCTTGGGCTCAAGC[A/G]ATCCTCCCACCTCAG | 10277 |
rs143391198 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10082036 | TATCCCTCCAAATTT[C/G]CTTGATATGTTTTAT | 10277 |
rs143392298 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10042792 | ATCAGATATGTGTAA[C/T]GTGTGCACTTTGAGG | 10277 |
rs143434517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161807 | GCCAGTACCAGTGCT[C/T]TTTCCTGACGTGCGT | 10277 |
rs143488428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090711 | AGGTATGAGCCACCA[C/T]ACTTGACCTTTTATT | 10277 |
rs143498107 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032484 | AATGAGCGCTCAATA[A/C]GGTAGATCACGCTCC | 10277 |
rs143511579 | snp | A/G | 0.000287568 | 0.0119875 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117584 | GAGTTGGAATAGAGG[A/G]AAAAAAAGCACCAAA | 10277 |
rs143515515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126285 | AGTCTGGGTGACAGA[A/G]CGAGACTCCGTCTCA | 10277 |
rs143548538 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | UBE4B | GRCh38.p7 | 1:10082982 | GTCCCTGCAAAGGAC[A/C]TGATCTCATTCTTTT | 10277 |
rs143556411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177121 | TCTGGATGCTAGGTC[A/G]TATCAGATGATACAT | 10277 |
rs143623070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061996 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTAAAG | 10277 |
rs143629080 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | UBE4B | GRCh38.p7 | 1:10139149 | GCCTGTAATCCCAAC[A/G]CTTTGGGAGGCCGAG | 10277 |
rs143656762 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10071140 | TCGAACTCCTGACCT[C/T]GTGATCCTCCTGCCT | 10277 |
rs143661736 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10147424 | TTTGAACCCGGGAGG[C/T]GGAGGTTGCATTGAG | 10277 |
rs143663738 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10040681 | GGAGTGCAATGGCGC[A/G]ATCTCAGCTCGCTGC | 10277 |
rs143678952 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072200 | CCCCAGCTACCTCCC[C/T]AATAGGTGCATCAGG | 10277 |
rs143689360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10040389 | GCTGGGATTACAGGT[A/G]TCAGCTACCACGCCA | 10277 |
rs143709546 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10157523 | GGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 10277 |
rs143744742 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10159107 | GATGACAGTGTTAAA[C/G/T]GAAGTTGTCAGAATG | 10277 |
rs143784553 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126834 | TGGCTCTTGCTGCCA[A/T]AGAGTGCTCCCTCGA | 10277 |
rs143806913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084662 | TTTCTTCGCCATCTC[C/T]CTTTAGTTTTCCTTT | 10277 |
rs143808422 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBE4B | GRCh38.p7 | 1:10062438 | CTTCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAT | 10277 |
rs143814870 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10103818 | TTTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 10277 |
rs143854107 | snp | C/T | 0.00102359 | 0.0225997 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178772 | GATAGTGGCCAAGAA[C/T]GCACGCGCAGAAATC | 10277 |
rs143870474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150272 | GTATGAAATTTTAAA[A/T]GTGACTCAAAAACGT | 10277 |
rs143875819 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10042961 | AGCATGGTTAGAGCC[C/T]TCTGTGCAAGGGGCA | 10277 |
rs143909066 | snp | C/T | 1.6522e-05 | 0.00287414 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178774 | TAGTGGCCAAGAACG[C/T]ACGCGCAGAAATCGA | 10277 |
rs143910951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10143643 | TCCCTCGAAGGATTC[A/G]GATGCGACAAGTTTG | 10277 |
rs143919339 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10065491 | GGTTCTATTTCCCCA[C/T]GCTGCAGGGGTAGTT | 10277 |
rs143963599 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10104389 | TGGTTTTTTTGGCCT[A/G]TCACTGGAATGTAAC | 10277 |
rs143984270 | in-del | -/AAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152259 | CAAGACTCCGTCTCA[-/AAT]AATAATAATAATAAT | 10277 |
rs144030352 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108435 | TTACCCCTGGAAACC[A/G/T]AGTGAAAAGCACTAC | 10277 |
rs144033579 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180040 | AGCGAAGCTGCCGTT[C/G]ATGTGTTGGAGGCCA | 10277 |
rs144040749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10060067 | CCTGTTCTATTCAGT[C/T]GTCAGGTCCCTGTGT | 10277 |
rs144068373 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10176147 | TAGCATCATGTTTCA[A/G]GGTTCATTTGTGTTG | 10277 |
rs144082826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048037 | ATTTTTATTAGAGAC[A/G]AGGGTCTCCCTGTGT | 10277 |
rs144114451 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10043719 | AGGCGTGATCCAACG[C/T]GCTGGGCCGGGATGC | 10277 |
rs144188727 | in-del | -/TT | 0.0701627 | 0.173662 | intron-variant | UBE4B | GRCh38.p7 | 1:10072243 | TCATACCTGGGACTC[-/TT]TTGTAATTCTTCTTA | 10277 |
rs144238509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10077235 | CTTTCTTCTGCCTTC[C/T]GATAGTTGCTGGCAG | 10277 |
rs144267748 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10052524 | TCATGTCTGTGATCA[C/T]GGTCTTTTGTTAGAC | 10277 |
rs144268120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128767 | CAGAGGAAATTAACT[A/G]TTGAAAATAATGTTT | 10277 |
rs144295618 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040832 | TCCATGTTGGCTTGG[C/G]GGGTCTCAAACTCTT | 10277 |
rs144304014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172432 | CAGAGAGGTTAAATA[A/G]CTTGCTCGAGGTCAC | 10277 |
rs144332718 | snp | A/G | 4.97129e-05 | 0.00498538 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179484 | ATCATGGACCGCTCC[A/G]TCATCCTGCGGCACC | 10277 |
rs144335241 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10124480 | AGTGTGAACCACAGC[A/G]CCTGGCCCAGACCTG | 10277 |
rs144341693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118017 | AGTGCAGTGGAACCC[C/G]GTATAACATAGGCAT | 10277 |
rs144373335 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10058938 | CTGTTGTCAAGAACC[A/G]TGAGGGCCAGATAAA | 10277 |
rs144399234 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10118143 | CTCAGTAAGCTACCC[-/T]TTTCCCATCACTTCT | 10277 |
rs144407536 | snp | A/C | 0.000115532 | 0.0075995 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103046 | GGACAGAGATGTCAT[A/C]TTTCTTTCTTCTCTT | 10277 |
rs144415598 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10063727 | AGCCTGGCCAACATG[G/T]TGAAACCCCGTCTCT | 10277 |
rs144415688 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149172 | AAATTGTCCTTTTTT[-/T]CTCTTTGACAGTATA | 10277 |
rs144479054 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10122814 | GCTGTATCATCACTT[C/G]CTTTTTTGTGACTAC | 10277 |
rs144498022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10150408 | ATTTATTCTCATTTT[C/T]AGCAGAGATTAAAAA | 10277 |
rs144504061 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102959 | CCAGGAGCCTTCCTC[A/G]GGCCCTGAAGTGTCT | 10277 |
rs144515212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074061 | CGTCTGCTTCAGTCT[C/T]TCATGTAGCTGGGAC | 10277 |
rs144585660 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10127672 | TTCTTACTGTATTTA[C/T]TTCTTTTACTTATTC | 10277 |
rs144606978 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10138422 | TATTTTTTGTAGAGA[C/T]GGGGTTTCTCCATGT | 10277 |
rs144616093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10060937 | TTTTTGTAGAGAAGT[C/T]ATCTTACTATGCTGC | 10277 |
rs144642695 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10166440 | CTTGTAGAGGCAGAG[A/C]GGCAGACCCGATAGG | 10277 |
rs144714224 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093673 | GTAACTCAAGTTTCT[A/C]TGTTTTCTTTTTTCA | 10277 |
rs144718535 | in-del | -/GTGTGTGTGTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155085 | AGAGAGAGAGAGAGA[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTT | 10277 |
rs144789395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075849 | TTGAGCCTAGGAGTT[C/T]GAGACCAGCCTGGGC | 10277 |
rs144823727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10133810 | GTTTCAGCTACTTGG[A/G]AGGCTGAGGCAAGAG | 10277 |
rs144858038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142180 | TTCCATCCTCAAATA[C/T]TAATTGTATCTTCAC | 10277 |
rs144865061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10063525 | AGTATCTCCAGAGCT[A/G]TCCCTTTCCTATGCC | 10277 |
rs144866368 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10056563 | TAAGCTGATAAATAC[A/G]TACTAATTCTAGTTG | 10277 |
rs144897486 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137183 | TATATCCGCAGACTC[C/T]GGGCTATCCGGGAGC | 10277 |
rs144910738 | snp | A/G | 6.58903e-05 | 0.00573941 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171254 | CTTTGAACCAAAGAA[A/G]CTGTTGGACCAACTG | 10277 |
rs144922095 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095265 | TGAAGTATATTGATA[A/C]CTTATGATTTCTTAG | 10277 |
rs144941878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034421 | CTCATTTCTTAAAGG[A/T]GTTATACAGATCTAC | 10277 |
rs144954622 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10138049 | AAGCGATTCTCCTGC[G/T]TCAGCCTCCCGAGTA | 10277 |
rs144964673 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108652 | CTTCATTCAATTCGA[C/T]GGTGTTCAGAAGAAT | 10277 |
rs144966569 | in-del | -/AGT | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10136005 | TACATAAATCCTCCC[-/AGT]AGTAACATTATTTAT | 10277 |
rs145005942 | in-del | -/ATAA | 0.158632 | 0.232706 | intron-variant | UBE4B | GRCh38.p7 | 1:10124730 | GAGAAATGTTCACAG[-/ATAA]ATAAATAGCAGCTAG | 10277 |
rs145011969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078340 | TATTTAAAATGTAGG[G/T]CTTACTGCAGGTCAG | 10277 |
rs145047884 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10119263 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCTCTAAG | 10277 |
rs145065333 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10037905 | AATGAGATTGCATAA[A/G]TGATTTTTCTCTCCT | 10277 |
rs145110390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142969 | AAAAATTAGCCAGGC[A/G]TGGTAACGCACCCCT | 10277 |
rs145145701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10151222 | CTCCCAAACCTACTT[A/T]TCCTGCCTTCCCCTC | 10277 |
rs145152684 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | UBE4B | GRCh38.p7 | 1:10075308 | GACCTGTCAGAAAAC[G/T]AGAAGCAGACCAGAT | 10277 |
rs145174224 | snp | A/G/T | 1.64738e-05 | 0.00286995 | synonymous-codon, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105667 | AGACAGAAATCTCTT[A/G/T]CTAAACACTGGCTCC | 10277 |
rs145199337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10055872 | TGCAGTGAGCTGAGA[C/T]TGCATCACTGCATTC | 10277 |
rs145199652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10044395 | CCACCAAGTGAATTA[A/G]GGCAGTGGTCCCCAA | 10277 |
rs145223511 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10158935 | GAATCACTTGAACCC[A/G]GGAGGCAGAATTTGC | 10277 |
rs145236182 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10150599 | GGGTGCAATGGCTCA[C/T]GCCTGTAATCCCAGC | 10277 |
rs145245181 | in-del | -/AATAATAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152260 | CAAGACTCCGTCTCA[-/AATAATAAT]AATAATAATAATAAT | 10277 |
rs145251464 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10174697 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA | 10277 |
rs145265842 | in-del | -/CACAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166966 | ACACACACACACACA[-/CACAC]AAAAAAAAAAAATTA | 10277 |
rs145266804 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100577 | TTATTTATTTGAGAC[A/G]GAGTTTCGCTCTTGT | 10277 |
rs145270088 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10050563 | TTATTTATTCACTTG[A/G]TGTAGCTCCTACTGG | 10277 |
rs145285992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114776 | GGCTGAGGCACAAGA[A/G]TTGCTTGAACCCAGA | 10277 |
rs145295804 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031146 | CCCAGGCTGGAGTGC[A/C/G]GTGGCACGATCTCGG | 10277 |
rs145319122 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10154578 | CTCAGTGACTCACGC[A/C]TGTAATCCCAGCACT | 10277 |
rs145406095 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108147 | TGGGATTTGGGGGAG[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs145426187 | snp | C/T | 0.0187336 | 0.0949518 | intron-variant | UBE4B | GRCh38.p7 | 1:10119504 | CTCACTTCCACCTTT[C/T]CTTTTCAGATGTGCA | 10277 |
rs145454581 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113857 | AGATCATGAGGTCAG[A/G/T]AGATCGAGATCATCC | 10277 |
rs145489974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134231 | GAATGTATAAAATGG[A/C]CAAGCGTGGTGGCTC | 10277 |
rs145543927 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10097024 | AGCCTGGGTGACAGA[A/G]TAAGACTCTGCATCA | 10277 |
rs145560492 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10168910 | AAAAAAAAAAAAAGA[A/G]GAAGAAAAAGCATAA | 10277 |
rs145560879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119331 | TTCTTTCTTCTCTGA[A/C]ATCAGTTTCTGCAGA | 10277 |
rs145571460 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10039136 | AATTTGAGTAGAGGA[C/G]ATAGATAGGAATCCA | 10277 |
rs145582816 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178743 | TTTAAGCTGCTCGCC[A/G]AGAAAGTGGAGGAGA | 10277 |
rs145639901 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10121577 | ATTTTCATCTTTTGT[A/G]GAGACAGAGTCTTGC | 10277 |
rs145640349 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105523 | TCCAACAGTATTCTC[C/T]GATTTTAAGGACTTG | 10277 |
rs145641209 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10133734 | CTGGCGACATAATGA[A/G]ACCCCATCTCTACAA | 10277 |
rs145648316 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UBE4B | GRCh38.p7 | 1:10176931 | GCTGGGACTACAGGC[A/G]TGCACCATCACGCCT | 10277 |
rs145655095 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10053510 | CCCAGGCTGGAGTGC[A/T]GTGGCACAATCAAGT | 10277 |
rs145705562 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10083716 | TGAGTTCAGGAGGCT[A/C]CTAGAAGAGGTTGAA | 10277 |
rs145733741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074967 | TTGGATGTCTAACAG[A/G]CATGTCACAGCTAGC | 10277 |
rs145749961 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10092540 | ACCCATTTCTTAAAA[G/T]AAGGAGGCCAGGCAC | 10277 |
rs145799711 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10075175 | CTGTAGCACAAAAGC[-/A]GCCATAGAACATATG | 10277 |
rs145843022 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10129900 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 10277 |
rs145856144 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10131347 | CCAGGCATGGCAGCG[C/G]GTGCCTGTAATCCCA | 10277 |
rs145863146 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10117006 | TGCCAAATGTTAGAT[G/T]AGGGCTTTTGAGATC | 10277 |
rs145907334 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | UBE4B | GRCh38.p7 | 1:10126352 | AGATAGATAGATAGA[A/T]AGAAAGGAGGAAATA | 10277 |
rs145909236 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10156487 | TCAAGTGATCTGCCC[A/G]CCCGGGCCTCCTGAA | 10277 |
rs145914083 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069593 | AGGCTGGAGTGCAGC[A/G/T]GTGCGATATTGGCTC | 10277 |
rs145974529 | snp | A/C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180067 | GCCAAATGTGGCAAA[A/C/G]CAACCCCAGGCCCAC | 10277 |
rs145996319 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10172158 | CGTGGGTCTCCTGTG[A/G]GCAGATCTGTCTGTG | 10277 |
rs146001182 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10048373 | GAGTTTGCAGTTCTT[C/G]GGGGAGGTTGGGGTT | 10277 |
rs146006634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065336 | CAGTTATGGGGCAAG[C/T]GGCGGGAGGAGCATG | 10277 |
rs146038319 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10132022 | GTAATCCCAACTACT[C/T]GGGAGGCTGAGGCAG | 10277 |
rs146042750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10051285 | AATACCATCTCGTAG[C/T]ACTGTTCTTCAGATT | 10277 |
rs146083700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132602 | TTGAACAAGGTAGAC[A/G]AGCTTCCTGCTTTTG | 10277 |
rs146125859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10066854 | GAGGTTGCAGTGAGC[C/T]AAGATCACGCTACCG | 10277 |
rs146166697 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | UBE4B | GRCh38.p7 | 1:10073047 | TGTAGACTATAGATA[C/T]ATATAAATGTTTATA | 10277 |
rs146205292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149066 | TATTTATTACATAGT[A/G]TTACAGAATGATTTT | 10277 |
rs146268739 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10047675 | TTTTTTCTATTTTTA[A/G]TAGAGATGGGGTTTC | 10277 |
rs146287463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10093038 | GCAGTATGTTACACT[A/G]TGTGATATACACTGG | 10277 |
rs146317821 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10167197 | GTAATCCCAACACTT[C/T]GGGAGGCCAAGGCAG | 10277 |
rs146360828 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10153127 | AGTTCTCCTGCAGCA[A/C]CCCCTATTGGCAACC | 10277 |
rs146367608 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10108207 | TCCCAGCCTCCACCG[C/T]CCCCCTGTTCACCCC | 10277 |
rs146401103 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10112366 | GGGAAAATATTAAAT[A/G]CTACTTTAAATATTT | 10277 |
rs146416067 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10176705 | TTGGGAGCAATGTCT[A/G]TTCATGTTCTTTGCC | 10277 |
rs146421763 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104878 | TAACCAAATCAGATA[A/C]AATTTCCATGAGTTA | 10277 |
rs146434563 | snp | C/T | 0.000264419 | 0.0114952 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178778 | GGCCAAGAACGCACG[C/T]GCAGAAATCGACTAC | 10277 |
rs146445179 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10063830 | GGAGAATCGCTTGAA[C/T]CAGGGAGGCAGAGGT | 10277 |
rs146476423 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10146599 | CAGCTCGTAAGAGGC[A/G]ACACTGGAATTCAGA | 10277 |
rs146544433 | snp | A/G | 0.00166099 | 0.0287704 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103090 | AGCAGAACCCAAAAG[A/G]AGGTAGGAATCTAGC | 10277 |
rs146545318 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | UBE4B | GRCh38.p7 | 1:10124909 | GGCAGGTGGATCGCC[G/T]GAGCTCAGGAGTTCG | 10277 |
rs146568292 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10082482 | TCCAGCCTGGACAAC[A/G]GAGTGAGACTCTGTC | 10277 |
rs146568866 | snp | C/T | 4.94336e-05 | 0.00497135 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119588 | CATACTGCTTTAGTA[C/T]TACAAGGCTCCCTAA | 10277 |
rs146586953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10078084 | GCACGATCTTGGCTC[A/G]CTGCAACCTCCGTCA | 10277 |
rs146587290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10128875 | GGTTGGATGTCTGAA[A/G]GAAAGTGTTGGAATT | 10277 |
rs146596609 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156234 | GTTTTGTTTCATTTT[-/C]TTTTCTTTTTTTTTT | 10277 |
rs146601338 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10143705 | GTTTCAGTTGTAGAC[A/G]AAAGAATCCAATTCT | 10277 |
rs146659821 | snp | C/G | 0.00100674 | 0.0224133 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178742 | ATTTAAGCTGCTCGC[C/G]GAGAAAGTGGAGGAG | 10277 |
rs146664538 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10142603 | TTGAACACGGGAGAC[A/G]GAGGTTGCAGTGAGC | 10277 |
rs146686475 | snp | C/G | 0.00135425 | 0.0259864 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179511 | CACCTGCTCAACTCC[C/G]CCACGGACCCCTTCA | 10277 |
rs146686896 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | UBE4B | GRCh38.p7 | 1:10103915 | ACAGGCATGAGCCAC[C/T]GTGCCTGGCCTCATT | 10277 |
rs146689339 | snp | A/G | 0.000441134 | 0.0148449 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135137 | TCCCAATGATGAGAC[A/G]CGTGTGAATGCAACG | 10277 |
rs146706099 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100277 | TACAGGTGTGAGCCA[C/T]CGTGCCTGGCCTATT | 10277 |
rs146745312 | snp | C/T | 0.362523 | 0.223246 | intron-variant | UBE4B | GRCh38.p7 | 1:10175422 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG | 10277 |
rs146766530 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10048175 | TGGGAGGCAACTAGC[-/T]TTTCTACCACAGGGA | 10277 |
rs146769102 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10085254 | CATCCCCTATCCTTA[A/G]TGAAGCAAAACTCCT | 10277 |
rs146791372 | in-del | -/AGAA | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10147670 | AAGTCTTTGATTGAT[-/AGAA]AGAGAAATCTATAAA | 10277 |
rs146802934 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10124264 | CCTTCTGGGTTCGAG[C/T]GATTCTCCTGCCTCA | 10277 |
rs146806000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043832 | GGTTATACCTGTTCA[C/T]GTAATCACCCCTTCA | 10277 |
rs146820409 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | UBE4B | GRCh38.p7 | 1:10162587 | TGCTGGGACTACAGG[C/T]GTGAGTCACCGCGCC | 10277 |
rs146820927 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | UBE4B | GRCh38.p7 | 1:10121279 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 10277 |
rs146824468 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10040411 | ACCACGCCAGGCCTC[C/T]GGCTAATTTTTGTAT | 10277 |
rs146866855 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10156010 | ACTCCAGCCTGGGCT[A/C]CAGAGTGAGACTCCA | 10277 |
rs146914935 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10089229 | CCAGGATGGTTTCGA[A/T]CTCTTGACCTCGTAA | 10277 |
rs146948394 | snp | C/T | 0.260227 | 0.249791 | intron-variant | UBE4B | GRCh38.p7 | 1:10163818 | ACTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGCG | 10277 |
rs146965071 | snp | A/C | 4.95462e-05 | 0.00497701 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161283 | GTGGGACCAGTTGCC[A/C]CGGGTGAGGACGTGG | 10277 |
rs146983740 | snp | A/G/T | 0.00554449 | 0.0523613 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106251 | GAGCTCTGTTCCCGT[A/G/T]ATGGGCCCGTCTCTT | 10277 |
rs147020193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10109634 | GGTCAGAGCCAAGAT[A/G]AGCTAGCAAAAAACC | 10277 |
rs147058919 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10110936 | ACGAGTTAGAGGCTG[C/T]AGTGAGTCGTGATCA | 10277 |
rs147070282 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10177776 | GCCAGTGTTTTTGCC[A/G]TATATGTTTTACTAT | 10277 |
rs147075073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106714 | TTAACCTGTGTGGCT[A/T]ACTAGTTTGGTAGGC | 10277 |
rs147077185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10049365 | AAGGGGGTACGGTTG[A/G]TGGGGCAGTTAATTC | 10277 |
rs147089781 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10126028 | ATAGAGGGCCAAGCG[C/T]GGTAGCTCATGCCTG | 10277 |
rs147093440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044846 | CCTCAGCCTCTCAAA[C/G]TGCTGGGATTACAGG | 10277 |
rs147138653 | snp | G/T | 6.59272e-05 | 0.00574101 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095464 | TTTTCTGTTTAGGAG[G/T]AGCCCATCGAAGCCA | 10277 |
rs147142759 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10123363 | TTGAACCAAGGAGAC[A/G]AGGTTGCAGTGAGCC | 10277 |
rs147179029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10077176 | GGCTAGAAGTCCAAA[A/G]CCAAGGTGTTGGTAG | 10277 |
rs147186349 | in-del | -/TTTAAG | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10125923 | AGCTCTTTGCTCTAA[-/TTTAAG]TTTAATGTAGTAATA | 10277 |
rs147212306 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10119266 | GTGTGAGCCACCGCG[C/T]CTGGCCTCTAAGGTT | 10277 |
rs147242366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10141639 | CTTCTGTTGCATCCA[A/G]TTTTGTAATAATGCC | 10277 |
rs147245303 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171185 | CTTTAATCTTCAGCA[A/G]CTTTGTGGCCCCAAG | 10277 |
rs147279900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098807 | CTCTCCTATTCAGTG[A/G]TGAGAAGTTAGCATC | 10277 |
rs147312858 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10135643 | CAGGAGGCTGAGGCA[A/G]GAGAATTGTGTGAAC | 10277 |
rs147316251 | in-del | -/G | 0.030665 | 0.119967 | intron-variant | UBE4B | GRCh38.p7 | 1:10035570 | CCCGGCTAGTTTTTT[-/G]TATTTTTTTGTGTTT | 10277 |
rs147329205 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147080 | CGCATCCTGGACCCC[A/G]CATATCCCGAGTGAG | 10277 |
rs147329353 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10175638 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 10277 |
rs147347701 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10106737 | GGTAGGCACGTACTC[-/T]TGAGTCCATGCTTCT | 10277 |
rs147349679 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10157100 | GGCTCACTGCAACCT[C/T]TGTATCTGGATTCAA | 10277 |
rs147353625 | in-del | -/AGACACAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144412 | GTGCCATCCATTCAA[-/AGACACAT]CATTGTTTTAGGAAC | 10277 |
rs147354815 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10081466 | GTCCCACTCTGTCAC[C/G]CAGGCTGGAGTGCAG | 10277 |
rs147374876 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10041752 | CCCATGCTGGAGTGC[A/G]GTGGCACGATCTCTG | 10277 |
rs147418518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154407 | AAGAGTGGATTTGGA[A/G]CTACGAGACAACAGC | 10277 |
rs147423649 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10077320 | CACATGGCCATCTTC[A/G]TTCTGTGTGTGTCTG | 10277 |
rs147480170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10062302 | AATTAAAAATACATT[C/T]GATGTGTGTTTTTTT | 10277 |
rs147494831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058345 | TGCCATTCTACCCCC[A/G]TCTGTTTCCACTCTG | 10277 |
rs147524786 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10173544 | TGCTTTACTAGCCCC[A/C]GACTATATAATACTG | 10277 |
rs147528251 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10099057 | AAGCCTAGCCAACAT[A/G]GTAAAACCCTGTTTC | 10277 |
rs147565397 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10073885 | CCATGCTCACTCTCT[C/T]AGCTAGTGGCCTGGC | 10277 |
rs147578811 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10169532 | GGCCTCCCTTAAAAG[A/T]TTGCAAAGTGCAAGG | 10277 |
rs147614640 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10110192 | TGCTGGCCCAGTGGA[G/T]TCGATGTCTTATAAA | 10277 |
rs147650975 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10115326 | AGGCTGGAGTGCAGT[G/T]GTGTGATCTCAGCTC | 10277 |
rs147716319 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10049434 | TTAGTCTTTAAAGAT[A/G]ACTAGGATTTTGACA | 10277 |
rs147718823 | snp | A/C | 0.00218849 | 0.0330069 | intron-variant | UBE4B | GRCh38.p7 | 1:10130663 | CCTTTTATTCAGATT[A/C]TTTCCCAAATGTGCA | 10277 |
rs147753372 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10053785 | GCCTCGACCTTTCGG[A/G]CTCAAGTGATCCTCC | 10277 |
rs147799328 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135150 | ACGCGTGTGAATGCA[A/G]CGATGGAAGATGTGA | 10277 |
rs147817631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10146408 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTTCAG | 10277 |
rs147821897 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10069598 | GGAGTGCAGCGGTGC[A/G]ATATTGGCTCACTGC | 10277 |
rs147854440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150550 | GTTTGGTTTTAAATC[G/T]GTCTTGTTACAGTGT | 10277 |
rs147878525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10053099 | CCACCTCAGCCTCCC[A/G]AGTAACTGGGACCAC | 10277 |
rs147924635 | snp | G/T | 0.194278 | 0.243711 | intron-variant | UBE4B | GRCh38.p7 | 1:10163583 | TGAGGCAGGATAATT[G/T]CTTGAACCCGGGAGG | 10277 |
rs147929279 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10089472 | TCTTGCCACTGTACC[A/G]CAGCCCAGGTATCAC | 10277 |
rs147948862 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10049163 | GAGACTTGAATATTA[C/T]TTAATTTGTTTGCTT | 10277 |
rs147961171 | snp | C/G | 0.0157785 | 0.0874088 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168162 | GGCTCGTCAGTCTCA[C/G]CTTGCTCAGGATGAG | 10277 |
rs147965451 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094669 | TCAATCTCCTGACCT[C/T]GTGATTCACCCGCCT | 10277 |
rs147975184 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10134309 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 10277 |
rs147996327 | snp | C/G/T | 9.88507e-05 | 0.00702969 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072171 | GAGTCTTGGTCTCAA[C/G/T]GTCCACAACATGACC | 10277 |
rs148011024 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10091494 | CTGTTGCCCATGCTG[G/T]AGTGCAGTGGTATGA | 10277 |
rs148019986 | in-del | -/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031098 | TATCCTGCAGGAGTC[-/T]TTTTTTTTTTGTGAC | 10277 |
rs148027900 | snp | A/G | 0.000148543 | 0.00861681 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158477 | CACCTTTATGGAGGA[A/G]TTCAAGTGAGTATGG | 10277 |
rs148029070 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10139291 | AGCTACTTGGGAGGC[C/T]ATAGCAGGAGAGTCG | 10277 |
rs148032713 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UBE4B | GRCh38.p7 | 1:10062099 | ATTTTTAGTAGAGAC[A/G]GTGTTTCACCATGTT | 10277 |
rs148081634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, stop-gained | UBE4B | GRCh38.p7 | 1:10107283 | GACAGTAGTGATGAA[G/T]AAGATGAAGAAGAAG | 10277 |
rs148091088 | in-del | -/AAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097055 | AAAAAAAAAAAAAAT[-/AAA]AATAATAATAATAAT | 10277 |
rs148098020 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10147451 | TGAGCCGAGATCATG[C/G]TACTGCACTCCAGCC | 10277 |
rs148108791 | in-del | -/GCGTGAGT | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10133121 | AAGGCAGCTGCAAGG[-/GCGTGAGT]GCTTCGGTCCGGGTG | 10277 |
rs148152253 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10153812 | AATTAGGCCTGGCAC[A/G]GTGGCTCACGCTGTA | 10277 |
rs148176574 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE4B | GRCh38.p7 | 1:10084699 | TTCTTTCTTTTCTTT[C/T]TTTTCTTTTTTTTTT | 10277 |
rs148182646 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10051840 | AGCAGGGGGAGAAAA[-/A]TCTCTGAATTGGATG | 10277 |
rs148188955 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10169876 | AAAAATTAGCCAGGC[A/G]TGGTAGTGCATGCCT | 10277 |
rs148221002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10156949 | CGATGTAGGAGGATC[A/G]CTTGAGGCAGGAATT | 10277 |
rs148225698 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10131434 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 10277 |
rs148276738 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10056609 | TTATTTCTGATGACT[A/G]TTTTATAAGATAAGA | 10277 |
rs148298206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065732 | AGTGGGAAATAATAA[C/T]GGTTTTCATTCTTTT | 10277 |
rs148360840 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10118309 | AGCCTTAGTGGAAGC[A/G]AAATGAGTGGGCATG | 10277 |
rs148366536 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10111773 | ACAAGCCTGGCCAAC[A/G]TGGCGAAACCTCTTC | 10277 |
rs148389459 | in-del | -/GTTT | 0.0248432 | 0.108648 | intron-variant | UBE4B | GRCh38.p7 | 1:10061266 | AAAACAAGTTTGTTT[-/GTTT]TTTTGTGAGACAGAG | 10277 |
rs148394301 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10145826 | TCACACAAAACCTAA[C/G]TATAGATGGGAATAT | 10277 |
rs148413280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081650 | CTGGAGTGTAATGGC[A/G]TAATCTTGGCTCGCT | 10277 |
rs148471735 | snp | A/G | 0.000214152 | 0.0103455 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119552 | CAGCTTCTGAGCAAC[A/G]TCCGCTCACAGTGCA | 10277 |
rs148483849 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082800 | TTGTCCTAATGCTCT[-/C]CCCTCCCCTTGACCC | 10277 |
rs148514322 | snp | A/G/T | 9.88377e-05 | 0.00702923 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147066 | TTCAGCTGCTGCTCC[A/G/T]CATCCTGGACCCCGC | 10277 |
rs148540121 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093736 | GTCTTGCTCTGTCAC[C/G]CAGGCTGCAGGGCAG | 10277 |
rs148550788 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10142263 | CCTGTTACCTATAAA[C/G]TCTTGTGATACCCGT | 10277 |
rs148602577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108735 | GATTCAGGAAGGTTG[A/T]TATTTGTATTACGCT | 10277 |
rs148618443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150313 | TTGAAAAACCAACCT[C/T]GGAATTTAAGCAACT | 10277 |
rs148680724 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10043340 | TTACTGAGATCTCAA[C/G]TGTTTTTCAATCATT | 10277 |
rs148692326 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UBE4B | GRCh38.p7 | 1:10162126 | GCCTCAGCCTTCTGA[A/G]TAGCTGGGATTACAG | 10277 |
rs148749176 | snp | C/G | 0.00119752 | 0.0244452 | intron-variant | UBE4B | GRCh38.p7 | 1:10052840 | AATTTGTTATTCACC[C/G]TTCTGCATTCTGGAG | 10277 |
rs148793136 | in-del | -/AAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152278 | ATAATAATAATAATA[-/AAT]ATAATAATAATAATA | 10277 |
rs148847340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10134237 | ATAAAATGGCCAAGC[A/G]TGGTGGCTCATGCCT | 10277 |
rs148864607 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10177104 | AAGAGTTCTTTATGT[A/T]TTCTGGATGCTAGGT | 10277 |
rs148868622 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10105996 | ACTACATCATTCTTC[A/G]AATGGGGACTTTATC | 10277 |
rs148905031 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10061741 | AATCAAGCCGCACCA[A/G]CAAAGCTGATGCTTG | 10277 |
rs148941818 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10084522 | GGGTGCATTTGTCTG[A/G]TCTTCCAAACTAGAT | 10277 |
rs149005794 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10122031 | ATATGGCTTCATTCA[A/G]GAACTGGTGAGAACC | 10277 |
rs149010267 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10130059 | TTTGAACTTCATCCA[A/G]TAGTATCCTGAAACT | 10277 |
rs149057218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10169571 | CATGAAACAAAACAG[C/T]TCACTGGCCAGACAC | 10277 |
rs149078737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143062 | GCAATGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 10277 |
rs149082080 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032184 | TGAGCCACCGCGCCC[A/G]GCCAAATATTTGTAT | 10277 |
rs149114612 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100993 | AAAGATGGACCATTA[G/T]CATTTTCCTTTCCTG | 10277 |
rs149145348 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10125012 | ATGCCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG | 10277 |
rs149148192 | snp | A/G | 0.248471 | 0.249995 | intron-variant | UBE4B | GRCh38.p7 | 1:10151032 | GCCGGGCATGGTGGC[A/G]GGTGCCTGTAGTCCC | 10277 |
rs149150733 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10044614 | CCGCCCGCCTGTCTC[A/G]CTTTGTCACCCAGGC | 10277 |
rs149215549 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10163310 | ACATTGGAACAATGC[A/G]GAGAAGATTACCATG | 10277 |
rs149248763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126718 | TGGACATTCAGTTCT[A/G]GCACCTTATTTGACA | 10277 |
rs149252997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047210 | ATTTGACTGCTGTGG[C/T]AGAGGTCGGAAATAA | 10277 |
rs149317597 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166010 | CCTGGCTGTTCTTGT[A/G]TCTTTCCTGGCTCTG | 10277 |
rs149343012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070985 | GGTGCCATCTCAGCT[C/G]ACTGCAATTGCCCTC | 10277 |
rs149354050 | in-del | -/TTTATTTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103400 | GAGCATTACCTCCTC[-/TTTATTTA]TTTATTTATTTATTT | 10277 |
rs149377085 | snp | C/T | 0.00443675 | 0.0468902 | intron-variant | UBE4B | GRCh38.p7 | 1:10135225 | GTCATTAAAACACTG[C/T]CCTCTTGTCTGTGTG | 10277 |
rs149396014 | snp | C/G | 1.6489e-05 | 0.00287128 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072080 | AGACCTCTCAGCCAA[C/G]CACCCCACTCACCTC | 10277 |
rs149397015 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10075735 | AAACAAACAGAAAAT[A/C]TCTCTTAAGACAGGT | 10277 |
rs149425040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10142167 | TGGGCTACCAGTGTT[A/C]CATCCTCAAATACTA | 10277 |
rs149441530 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10179101 | TTTCAAAGAATTCCC[A/T]GAAGTCCTAAGACAA | 10277 |
rs149466248 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | UBE4B | GRCh38.p7 | 1:10086072 | CACCTCCCTGGTTCA[C/T]GCCATTCTCCTGCTT | 10277 |
rs149582683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10172336 | TTTCACCCACTTTTC[A/G]TATCTCCACCCATTT | 10277 |
rs149587415 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10098186 | TTGCTTTAAAATAAT[A/T]CAATATAATATAAAT | 10277 |
rs149604270 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10144607 | GGGCATGGTGGTGAG[A/C]ACCTGTAATCCCAGC | 10277 |
rs149605508 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBE4B | GRCh38.p7 | 1:10035995 | GTGATCCGCCCGCCT[C/T]GGCCTTCCAAAGTGC | 10277 |
rs149618075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156918 | TCACACCTGTAATCT[C/G]AGTACTTTGGAAGGA | 10277 |
rs149622283 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10079349 | ATTTTTAGTAGAGAC[A/G]GAGTTTCACCATGTT | 10277 |
rs149655242 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10113761 | TGGCAAGGACCTATT[G/T]ACATCAAACATAAGA | 10277 |
rs149678973 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10160612 | TGCAAGGTGGCTCCA[A/G]ATACCACTGGAATGA | 10277 |
rs149691338 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10067639 | TTTTTTTTTTTGAGA[C/T]CCGGCTCTCACCGGG | 10277 |
rs149707579 | snp | C/G | 0.029116 | 0.117091 | intron-variant | UBE4B | GRCh38.p7 | 1:10038993 | TAAACTCAGGAGACA[C/G]AGGTTGCAGTGAGCC | 10277 |
rs149708700 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10119277 | CGCGCCTGGCCTCTA[A/T]GGTTCTTAAGTATAA | 10277 |
rs149725744 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10158878 | AACTGGGTGTGGTGG[C/T]GCACGTCTGTTATCC | 10277 |
rs149760840 | snp | A/G | 9.9318e-05 | 0.00704621 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10121970 | TCCACAGGTCCTTGC[A/G]GCAGCCGTCCTTCCT | 10277 |
rs149847913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10167880 | ACGCGTGAGCCACCA[C/T]GCCCGGCAGATGGTG | 10277 |
rs149849363 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10063148 | TGGCGCATGCCTGTA[G/T]TCCCAGCCACTGGGG | 10277 |
rs149866431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073632 | GGCTGAGGCATGAGA[A/G]TTGCTTAAACCCGGG | 10277 |
rs149899336 | snp | A/G | 0.000610224 | 0.0174568 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151530 | TCTCTCCACCAAGTT[A/G]TTGGTACCTTCCCTG | 10277 |
rs149900579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137396 | TGGTGAAGTGATCCA[A/G]ACCTTGATTTCTGAG | 10277 |
rs149915029 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10150026 | CACAGAATACAAATT[G/T]TGAAAGTTTTGTAAC | 10277 |
rs149920000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077640 | TGTTAGAAGCGAAGT[A/G]AGATTTGAGTTCTTT | 10277 |
rs149936557 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10124237 | CGCCGTCTCAGCTCA[C/T]TGCAACTTCCACCTT | 10277 |
rs149984077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10162829 | GTTATTCCCGTCTCC[A/G]TCCATGTGTACCAAT | 10277 |
rs149987861 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10088194 | TCCTGGTCTACTGAC[A/T]CCAGATGTATGATTC | 10277 |
rs150061339 | snp | C/G/T | 0.00019933 | 0.00998137 | intron-variant | UBE4B | GRCh38.p7 | 1:10102925 | TTATTTGAAATTAAC[C/G/T]TGCAAATCTTCTTCT | 10277 |
rs150088068 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UBE4B | GRCh38.p7 | 1:10091723 | CGATTCTTCTGACTC[A/G]GCCTCCCTAGTAGCT | 10277 |
rs150090746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165255 | CTTCATTCTACCAGC[G/T]GCTCAGGCTCGATGC | 10277 |
rs150151977 | snp | A/G | 6.60829e-05 | 0.00574779 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179955 | AGAACAGCGATCACT[A/G]AACCGTTCCGCCGCC | 10277 |
rs150212272 | snp | A/G | 0.291235 | 0.246576 | intron-variant | UBE4B | GRCh38.p7 | 1:10175442 | GGATCACAAGGTCAG[A/G]AGATCGAGACCGTCC | 10277 |
rs150213717 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10069875 | GAAGCAGAGAGCTGT[G/T]AAGTGACTTATCTGG | 10277 |
rs150230101 | snp | A/C/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10116577 | TATGTATATCAAATC[A/C/G]GTTTGTGAGTTAAAC | 10277 |
rs150281653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040808 | TATTTTTATTAGAGA[C/T]GGGATTTCTCCATGT | 10277 |
rs150282608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10122346 | AATATGTAAGGCCCC[A/G]TTCCTGATTTCAAGG | 10277 |
rs150299536 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10131769 | CAGCCTGACCAACAT[A/G]GTGAAACCCCATCTC | 10277 |
rs150335709 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10085710 | AGGTAGTAAGAACAA[A/G]TACAGAGTTCACTAA | 10277 |
rs150369724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064614 | TTCAGTTCCACTCTC[C/T]ATCACCTCGTCTCTT | 10277 |
rs150372887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142737 | CTTTGCCTTTTCCAT[C/T]TTCTGAAAGCTGCCT | 10277 |
rs150420533 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10139785 | CCAGGCAGGAGTGCA[A/G]TGGTGCAATCTTGGC | 10277 |
rs150442851 | snp | A/G | 0.00516435 | 0.050552 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105713 | CCCATGTTCTGCAGC[A/G]TGGCTTCCTTTGGTG | 10277 |
rs150461556 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094902 | TTCAAAGGATTCTCC[A/T]GCCTCAGCTTCCTGA | 10277 |
rs150494373 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBE4B | GRCh38.p7 | 1:10079207 | TTTGAGATGGAGTCC[C/T]GCTCTGTCGCCCAGG | 10277 |
rs150528649 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10113349 | GTCACCTCCCACTAG[G/T]CCCGTGCTCCAACAC | 10277 |
rs150544410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154078 | CAAGAGCAAAACTCC[A/G]TCTCAAAAACAAAAA | 10277 |
rs150563488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097229 | AAAGCAGATGAAAAA[C/T]ATAAAAGATATTTAG | 10277 |
rs150598117 | snp | C/G | 0.0189929 | 0.095638 | intron-variant | UBE4B | GRCh38.p7 | 1:10157639 | AAAAATTAGCAGGGC[C/G]TGGTGGCGCATGTCT | 10277 |
rs150613900 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10167295 | AAATACAGAATTAGC[C/T]GGGCATGGTGACACA | 10277 |
rs150616370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10062496 | TTTTGTATTTTTAGT[A/G]GAGACGAGGTTTTGC | 10277 |
rs150680333 | snp | G/T | 0.0020388 | 0.0318629 | intron-variant | UBE4B | GRCh38.p7 | 1:10178841 | GACTCGTCGTTTTCA[G/T]GCTGATTTCTTTTGA | 10277 |
rs150684696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107878 | TCACTGTGTCTGGCC[C/T]CAGAATTTTCAGAGT | 10277 |
rs150736740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073393 | AACCATTTGAACTAA[C/T]TGAAAACTTTTGAAA | 10277 |
rs150753108 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | UBE4B | GRCh38.p7 | 1:10118786 | TGGGATTACAAGTGT[A/G]AACCACTGCACCCGG | 10277 |
rs150771997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10058080 | GCTGAGGCCAGGAGC[C/T]GACATGGATGATCCC | 10277 |
rs150774269 | snp | A/G | 0.000132044 | 0.00812431 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135021 | TCTACAGATGGATTT[A/G]TGCTGAATTTCCTTT | 10277 |
rs150805888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10123746 | ATGAAATTCATATAA[C/T]ATCAAACCACCGTTG | 10277 |
rs150809853 | snp | C/T | 0.079617 | 0.182947 | intron-variant | UBE4B | GRCh38.p7 | 1:10043519 | GCAAGCTCCGCCACC[C/T]GGGTTCACACCATTT | 10277 |
rs150823000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133000 | ATCAGAACTGTCATG[A/G]GAGGGTTTTCAGCAG | 10277 |
rs150856019 | snp | A/G | 0.000131789 | 0.00811648 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161190 | GTTGATAAACGACAC[A/G]ACGTTTTTGCTCGAT | 10277 |
rs150896976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144362 | CAATGTACTTTCTTG[C/T]AACAAAAAAGATGAT | 10277 |
rs150907063 | snp | C/T | 3.37365e-05 | 0.00410696 | splice-donor-variant | UBE4B | GRCh38.p7 | 1:10178820 | TGATGAGTTCAGAGG[C/T]AAGTGGACTCGTCGT | 10277 |
rs150945622 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | UBE4B | GRCh38.p7 | 1:10142584 | GTTGAGGCAGGAGAA[C/T]CGCTTGAACACGGGA | 10277 |
rs151001500 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10038035 | CCTGTAATCCCAGCG[C/T]TTTGGGAGGCCGAGG | 10277 |
rs151033703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093954 | CCTTCCTCGGCCCCT[C/T]AAAGTGCTGAGATTA | 10277 |
rs151050654 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10116163 | TTTCTTTTATTTTAG[C/G]ACAGCGTCTCTCTTT | 10277 |
rs151067992 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10155318 | AGCCACCACTTATTG[A/C]ATGCTTACTAATCCT | 10277 |
rs151140088 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBE4B | GRCh38.p7 | 1:10064358 | TGAAAAAAAGGTGAT[A/G]CTCTATGCACAAGCA | 10277 |
rs151158190 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10175929 | CACAGCCACCACCTC[C/T]ACCTAGTTCCACTAC | 10277 |
rs151208851 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109313 | CCGTGCTGCCACCCA[C/T]TTTTCCATTTCTGCC | 10277 |
rs151250362 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10157796 | AATAATAATAATAAT[-/A]AAAATTTGTCATGAA | 10277 |
rs151261927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074755 | CTTTTCATTTCCCTG[A/C]CTTCTAAATGTTAGG | 10277 |
rs151302350 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10120089 | GAGAATCCTATAAAG[A/G]TTGCAAATTTTTGTT | 10277 |
rs151330704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125669 | TCTATTTAATGTTAT[G/T]AGCCTTGAATCCCAA | 10277 |
rs180741864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036740 | TTGTTACTCTGTAGT[G/T]GAAAACTTGTGTCAG | 10277 |
rs180788576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173346 | AATTAGCCGGGCGTG[A/G]TGGCGGGCGCCTGTA | 10277 |
rs180968554 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10115358 | CAGCAGCCTCTGCCT[C/T]CCGGGATTTAAGAGA | 10277 |
rs180972857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069974 | CCTAAATTTAGCTGT[C/G]TGTAAGATAATGAAA | 10277 |
rs180972998 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10089589 | TTCCGTGAATATTAA[C/T]GCTTTAGCTTAATTC | 10277 |
rs180980483 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10135528 | CAGATCAAAAGGTCC[A/G]GAGTTCATGACCAGC | 10277 |
rs180983516 | snp | A/G | 0.00184011 | 0.0302765 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106379 | CATCCCCGCGGTATC[A/G]CCCCTACACTGTCAC | 10277 |
rs180997415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048303 | CTGGTTTGAACATAT[G/T]ATGAATATGCTGCCT | 10277 |
rs181012032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056723 | GCCAGCGCTAGCTAC[A/G]CGATTGCTCATTGTG | 10277 |
rs181029808 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10077256 | TTGCTGGCAGTCCTT[A/G]GCATTTCTTGGCTTG | 10277 |
rs181031931 | snp | A/C/T | 0.0411944 | 0.138227 | intron-variant | UBE4B | GRCh38.p7 | 1:10175613 | CCGAGATCGCGCCAC[A/C/T]GCACTCCAGCCTGGG | 10277 |
rs181046062 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147736 | CCTCCTAAGCACTGG[A/G]TCCAGGAATACCCAC | 10277 |
rs181050360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157894 | ATAGATTTAGGGATG[A/T]TAGACACATTGGTGT | 10277 |
rs181052402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162173 | CTGGCTAGTTTTTGT[A/G]TTTTGTTTGTTTGTT | 10277 |
rs181054739 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10125057 | CTTGAACCCGAGTGA[C/T]GGAGGCTGCATTTAG | 10277 |
rs181057282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142238 | CAGAGCCCCATTTTT[C/T]TCATGAAGGCCTGTT | 10277 |
rs181078425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10168808 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 10277 |
rs181082796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119156 | AAAGTGCTGAGATTA[C/T]AGGCGTGAGCCACCG | 10277 |
rs181086651 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181001 | ACAAACACAGCCACA[C/T]GCGCACACAAGTATA | 10277 |
rs181090814 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | UBE4B | GRCh38.p7 | 1:10150863 | AGGCTCCATCTCAAG[A/G]AAAAAAAAAAAAAAT | 10277 |
rs181107294 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10109963 | CTCGGCCTCCCAAAT[C/T]GCTGGGATTACAGGC | 10277 |
rs181120386 | snp | C/G | 0.00196151 | 0.0312563 | intron-variant | UBE4B | GRCh38.p7 | 1:10130458 | ATTTTTACCCCACCG[C/G]CCTGTTCAGCGGCTT | 10277 |
rs181125840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085698 | ACAGAGAAACTGAGG[C/T]AGTAAGAACAAGTAC | 10277 |
rs181129664 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102514 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10277 |
rs181130884 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172413 | TAAAGTGAGGAAAGA[C/G]GCACAGAGAGGTTAA | 10277 |
rs181226243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053493 | TGGAATTTTGCTCGT[C/T]GCCCAGGCTGGAGTG | 10277 |
rs181226464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074653 | TTCTCCTGGAAACAC[A/G]TTTTTCTTTTGGCTT | 10277 |
rs181248760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10093483 | CTTATTTCCTTCATA[A/G]ATCCTGCAGAAGTTT | 10277 |
rs181261739 | snp | C/T | 1.83538e-05 | 0.00302929 | intron-variant | UBE4B | GRCh38.p7 | 1:10168299 | CGGGGCTCTGTTTGG[C/T]GGTTTGGACTCCACA | 10277 |
rs181279170 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031153 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCCTTG | 10277 |
rs181305266 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063850 | GAGGCAGAGGTTGCA[A/G]TGAGCCGAGACCATG | 10277 |
rs181344956 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10068374 | TTTTTTTTTGAGCAG[A/G]AGTCTCGCTCTGTTG | 10277 |
rs181351852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146777 | GTGGTTTGCTTGCCA[C/T]GCCTTTGTTTTTCTC | 10277 |
rs181426516 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124385 | CAGGCTGGTCTTGAA[C/T]TCTTGGCCTCAAGGC | 10277 |
rs181464176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158981 | TGCCAGTGCTCTCCA[C/G]CCTGGGTGACAGAGC | 10277 |
rs181475077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088998 | TTATTTTTGTTTAGT[C/T]ACAAGAACAAAATGT | 10277 |
rs181477543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136823 | TACTAGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 10277 |
rs181523675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052605 | GCAGAGGTGCCCCAC[A/G]CTTGGTTTAATGCTC | 10277 |
rs181617414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084471 | AAAAGGCCTATAACC[A/G]GTAGAGATCGTGCCA | 10277 |
rs181627453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10175947 | CTAGTTCCACTACAT[A/G]TATCACCCCAAAAGG | 10277 |
rs181632674 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10101799 | GGCGTGAGCCACTGC[A/G]CCTGGCCTGGTCTTT | 10277 |
rs181637065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10118738 | CTAACTCCCGACCTC[A/G]TGTGATCTGCCCACC | 10277 |
rs181645194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041185 | CAGATAAGAAAATGG[A/T]GGCTAATAGAAATTA | 10277 |
rs181659357 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10063220 | TTGCAGTGAGCTGAA[A/G]CCGTGCCTCTGCACT | 10277 |
rs181676858 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10161399 | ATGCGATCTGACATG[A/C]TGGGATTTTCCTTCC | 10277 |
rs181689442 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140579 | TGTTTCTTTATCCTC[C/T]GATGGATTACCTCCT | 10277 |
rs181837118 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10088524 | GGGATCACAGGTGCC[C/T]GCCACCATGCCCAGC | 10277 |
rs181846193 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10037007 | TTGGTCCCTGTCATA[A/G]ATCACCTAGAATTCT | 10277 |
rs181847403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105182 | TTAATATACATCAGC[A/G]GTAACTCTCAATGAC | 10277 |
rs181850870 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10057204 | CAGTTTTATGCCTTT[C/G]GTCCTTAGTTCTCAC | 10277 |
rs181855359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10123766 | AACCACCGTTGTTGT[C/T]TTGTTTTGTTTTGTT | 10277 |
rs181869557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046816 | AACCCTACTTAGCCC[C/T]AAATTACCAGACTCT | 10277 |
rs181869761 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10067919 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 10277 |
rs181876788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040458 | GTCTTGCCATGTTGC[C/T]CAGGCTGGTCTCAAA | 10277 |
rs181891239 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | UBE4B | GRCh38.p7 | 1:10062958 | TGAAACTCCGTCTCA[A/G]AAAAAAAAAAAAAGA | 10277 |
rs181945943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10115933 | TATGGCATTATAACC[C/T]TGTGGGACCACTAGG | 10277 |
rs181951298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158696 | TTTGTCAAGATACTT[C/T]GGGGGTGGTACACAA | 10277 |
rs181978093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10152712 | CCGAGGCACGAGAAT[C/T]GAGTGAACCTAGGAG | 10277 |
rs181993636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093797 | CCTCCCAAGTTAATG[C/T]GATTCTCCTGCCTGA | 10277 |
rs182074042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10078156 | TGGGGTTACAGGTGC[A/G]TGCCACCACACCTGG | 10277 |
rs182106820 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074047 | AGGCTCAGATGATCC[A/G]TCTGCTTCAGTCTCT | 10277 |
rs182121880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133343 | CAGTGACTCCTCTGT[A/G]CCTCCATTTCCTCAT | 10277 |
rs182131511 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180118 | GACCTGAAAGGACAT[A/G]GATGAGAAGAGGAGC | 10277 |
rs182139924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175104 | AGGCTGACAGAAAGG[G/T]GCCTGGGTGAAGAGC | 10277 |
rs182143069 | snp | A/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031595 | GTTCTGGCTTACACA[A/G]AATTCCTTTCCTGGA | 10277 |
rs182149127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156804 | ATAGGTGTTAATTAT[C/T]TTATTTTATTTTTAA | 10277 |
rs182155244 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10113899 | GTGAAACCCCGTCTC[A/T]ACTAAAAATACAAAA | 10277 |
rs182172158 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140446 | CACATATATTATTTA[G/T]GTCAAGTTTGTTAAT | 10277 |
rs182207323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101286 | TAGATTGGGGCCACC[C/T]GAAATCAGGAAGTCC | 10277 |
rs182207436 | snp | C/T | 0.000116656 | 0.00763639 | intron-variant | UBE4B | GRCh38.p7 | 1:10179873 | ATCTGGGGCATTAAT[C/T]CTCCTTTTTTTCTTT | 10277 |
rs182213320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074729 | TTCCTTCTTCACTCT[G/T]TGCCTGGTTCCTTTT | 10277 |
rs182219944 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098444 | AATATTCCACAGGCT[C/T]CCCAGAATTTCCCAT | 10277 |
rs182234182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136618 | TAAGTTTATAATTGC[A/G]AAAGTATCCTTAAAC | 10277 |
rs182336649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10108313 | ATGTCTAGCCTTAAA[C/T]TTCTCTTAGCACCTC | 10277 |
rs182341369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10127350 | CTGTTTCCTAAGGTC[A/G]TATTTACTTGGGAAG | 10277 |
rs182344197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176977 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10277 |
rs182350136 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10159395 | TCCCATCTAAGGGCC[A/G]GGCGTGGTGGCTCAT | 10277 |
rs182380922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10112431 | TTTAGACGGAGTCTC[A/G]CTCTGTCTCCCGGGC | 10277 |
rs182385943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035032 | GAGACGGAGTCTTGC[C/T]CTGTCGCCCAGGCTG | 10277 |
rs182397985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075532 | CATATGCTGTTATCA[C/G]AAACTAACAGAAAGG | 10277 |
rs182399459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055037 | GGGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 10277 |
rs182416448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10083992 | TTTTGACTTGGGGTT[A/G]ATTCTTGCACTTTTC | 10277 |
rs182424461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10133123 | GGCAGCTGCAAGGGC[A/G]TGAGTGCTTCGGTCC | 10277 |
rs182479772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118270 | CATATTTGTAAAGGG[A/C]CTTCTTTGGGCTTTG | 10277 |
rs182479820 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160815 | GGGCGTGGTGGTGTG[C/T]GCCTGTAGTTCCAGC | 10277 |
rs182484657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142610 | CGGGAGACGGAGGTT[A/G]CAGTGAGCTGAGATT | 10277 |
rs182501688 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076161 | TCCTGGAAGTTAGAC[A/C]TAGGTCTAATGGGTA | 10277 |
rs182574595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078968 | ACTACAGGTGCGCGC[C/T]ACCATGCCTGGCTAA | 10277 |
rs182577068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099246 | GACTCTGTCTAAAAA[A/G]GAAAAAATTATTTAC | 10277 |
rs182577630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165806 | CCTGACTCCTGACCC[C/T]GCTTCATTTTTCCTC | 10277 |
rs182584249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171520 | GGAGGCCAAGGCAGG[A/G]GGATTGCTTGAGGCC | 10277 |
rs182589578 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10116181 | AGCGTCTCTCTTTGT[C/G/T]GCCCAGGCAGGAGTG | 10277 |
rs182595716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10038160 | TGGCACATGCCTGTG[A/G]TCCGAGGTACTCAGG | 10277 |
rs182608326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057888 | GCCTTGCCTGCATTC[C/T]GGTGGCAGGGAAGCA | 10277 |
rs182692617 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060488 | ATTGACTGAAATGTC[C/G]TTATGCAGCCCATGA | 10277 |
rs182731522 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10163181 | CTCCTGCCTCAGCCT[C/T]TGTAGATCCAAAGAG | 10277 |
rs182759701 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099817 | ATAGACCCACTCGTT[A/G]ATGAAAATTGGACAC | 10277 |
rs182772836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095291 | CTTAGTAATGTTCCT[A/G]TGATTTTATTATTGT | 10277 |
rs182834239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10155159 | CTGTTGCCTATAAGA[C/T]GAGTGCTGGGCCTAG | 10277 |
rs182871049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149639 | ATTTTGTACTAAAAT[G/T]TGTCTCAATTGTAAA | 10277 |
rs182968585 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10038204 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 10277 |
rs182969387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10042260 | GTCTTCCTGTAAACG[A/G]TTCATTCAACAGCGC | 10277 |
rs182978540 | snp | G/T | 0.0314385 | 0.121371 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032713 | AGTCGTCCCTCCCCT[G/T]GCCAGCCTACCTGGC | 10277 |
rs183032478 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10080217 | ATGAGGTCAGGAGAT[G/T]GAGACCAGCCTGGCC | 10277 |
rs183051112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10116339 | GTAGAAACAGGGTTT[C/T]GCCCTGTTGGTCAGG | 10277 |
rs183055051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10165249 | TGGCGCCTTCATTCT[A/G]CCAGCTGCTCAGGCT | 10277 |
rs183069717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071462 | ACATGGTGGTTTGCA[C/T]CTGTAGTGTTAGATA | 10277 |
rs183129727 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10174673 | TGCCATTGCACTCCA[A/G]CTTGGGCAACAAGAG | 10277 |
rs183167230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10103973 | CACCATGTTGGCCAG[A/G]ATGGTCTCGATCTCT | 10277 |
rs183175410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10121350 | ACAGAGCGAGACTCC[A/G]TCTCTAAAAAACAAC | 10277 |
rs183191176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144369 | CTTTCTTGCAACAAA[A/G]AAGATGATTATATTC | 10277 |
rs183194606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065051 | TAAAGGTGTGAGCCA[C/T]CGCGCCTGGCCCTAA | 10277 |
rs183197475 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10086800 | GTTCAAGCAATTCTC[C/G]TGCCTCAGCCTCCCA | 10277 |
rs183209673 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10061077 | TTCTGTTTTTTTTTT[A/T]ATCTCAAAAGACAAC | 10277 |
rs183211109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107051 | CCAGTGGCCCCTTCT[C/T]TCAAATGTACCTGTA | 10277 |
rs183215154 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081025 | ATAAATAATAACGTT[G/T]TATATATTTTTTAAA | 10277 |
rs183218407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10125967 | TGTTGGCCTGTTTAT[C/T]TTGTTTTCCTCAAAA | 10277 |
rs183231533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148413 | GAGGCAGGCGGATCA[C/G]TTGAGGTCAGGAGTT | 10277 |
rs183256073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090918 | ATCATTCAGGAAATA[A/T]TACAATACTAGGAGA | 10277 |
rs183256100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038805 | GTCGCGTTAAAAATT[C/T]GGGAGTTGGGGCCGG | 10277 |
rs183269897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10169116 | TAAGACCTGGTTCCT[A/G]TTTCTAAAATTGAAA | 10277 |
rs183316758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050979 | CAGAGTTCTAATTCA[C/G]AGTCAGACATACTTG | 10277 |
rs183358762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108036 | ATTGCGAGAATGTTA[G/T]TGTGAACTACCAGAT | 10277 |
rs183414389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064873 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCT | 10277 |
rs183448697 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10085941 | ATTACAGGCACCCAC[C/G]ACCACGCCCAGCTAA | 10277 |
rs183471331 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10042504 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGCAC | 10277 |
rs183539661 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10054227 | AATATCTGGCTGTTT[C/T]CTAACCAATTGAGTA | 10277 |
rs183546233 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10088291 | GTGATTTTCTAATTC[C/T]GGCTGTTGGTTTTCT | 10277 |
rs183549774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105015 | AGCCACATGGTGACT[A/G]GATGTTGGACCCTTC | 10277 |
rs183571527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045461 | ACTCTGTCCTTGTCT[G/T]TTGTTCAGGCATTTT | 10277 |
rs183583941 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10066395 | CAGCCTCCCAGAGTG[C/G]TGAGATTACAGGTGT | 10277 |
rs183590871 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10091204 | GTTCATTTTTTAATT[A/C]TTTAATATCTGGCTT | 10277 |
rs183600964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10170125 | TGTGATGTTTTCATT[G/T]CCTTTGCTACACTAT | 10277 |
rs183604509 | snp | A/G | 0.000115627 | 0.00760264 | intron-variant | UBE4B | GRCh38.p7 | 1:10126910 | TTCTTTAACTCATTC[A/G]ATAGATGTTTTTCTT | 10277 |
rs183622536 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094040 | TTTTCAGCACCATAG[G/T]TATATATATTTTAAA | 10277 |
rs183626245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174466 | AGCACTTTGGGGAGC[C/T]GAGGCGGGCAGATCA | 10277 |
rs183635968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131901 | GAGGTTGCACTGAGC[C/G]GAGATGTGCCACTGC | 10277 |
rs183670071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048955 | TTTATTCATTCAACA[C/G]TCTGTTTCTCTCTCT | 10277 |
rs183693568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160105 | TTTTTTTCTCTACGA[A/G]TCTGGCATCTCCAGA | 10277 |
rs183722050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116892 | GTCTTTTACTATACT[A/G]CTTTACCTTTTTCAC | 10277 |
rs183754258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10092287 | CGGAGTGCCGTGGCA[C/T]GATCTTGGCTCACTG | 10277 |
rs183771579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175623 | GCCACTGCACTCCAG[C/T]CTGGGCGACAGAGCG | 10277 |
rs183774008 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10158226 | GCCCTACATGCAAAA[A/G]AAGTGCAAAATTTCA | 10277 |
rs183790914 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10074882 | ATGATTCCTAAGCTT[A/T]TATCTCCAACGTGGA | 10277 |
rs183799536 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10051481 | TAGTGGTATCTTACT[A/G]GTTAAGGTAGCAAAT | 10277 |
rs183801362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10071683 | TACAGTATATACGTA[C/T]TTATGTATGTATTTA | 10277 |
rs183828795 | snp | C/T | 0.000553278 | 0.0166233 | intron-variant | UBE4B | GRCh38.p7 | 1:10179403 | TAGAGTTTGCTTTGC[C/T]TTGTCCCCGCAGACC | 10277 |
rs183835001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160662 | AAAGAATAACAAAAT[C/T]CAGGCCAGGTGTGGT | 10277 |
rs183841219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043482 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG | 10277 |
rs183844721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10111682 | AAATGCAAGGCCAGG[C/T]GCGGTGGCTCACACC | 10277 |
rs183854621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153692 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT | 10277 |
rs183880201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100268 | TGCTGGGATTACAGG[C/T]GTGAGCCATCGTGCC | 10277 |
rs183888778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070539 | CCAAGGATAACCATT[A/G]TCCAAACTAATGGTA | 10277 |
rs183941051 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10138059 | CCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10277 |
rs183948745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177807 | AAATACAAACTACAG[C/T]ATACTTTACTGTTTG | 10277 |
rs183958340 | snp | G/T | 0.000446366 | 0.0149326 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103062 | TTTCTTTCTTCTCTT[G/T]CTGCACAGTTTAAGC | 10277 |
rs183986145 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10036433 | CAAAGGGCTGGTTCA[A/G]TAACTGTTAATTTTA | 10277 |
rs184020973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115211 | GGCTGGTCTCGAACT[C/T]CTGACCTCAAGTGAT | 10277 |
rs184035122 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10135420 | ACCAGCCTGACCACC[A/G]TGGTGAAACCCCGTC | 10277 |
rs184041999 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10157678 | AGCTACTAGGGAGGC[C/T]GAGGCAGGAGAATTG | 10277 |
rs184043763 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10056470 | TACTGTCATAGTTGC[C/T]GGGAATACAGCGGTG | 10277 |
rs184059108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076905 | GCGCCTGCCACCACG[C/G]CTGGCTAATTTTTGT | 10277 |
rs184059384 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096848 | GTTCAAGACCAACCT[C/G/T]TCCAACATCGTGAAA | 10277 |
rs184119926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055752 | TGGTGAAACCCTGTC[A/T]TTACTAAAAATACAA | 10277 |
rs184319531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145810 | AATTGAAATTGATTC[A/G]TCACACAAAACCTAA | 10277 |
rs184335036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124230 | GCAGTGGCGCCGTCT[C/G]AGCTCACTGCAACTT | 10277 |
rs184365621 | snp | C/T | 3.30699e-05 | 0.00406618 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168210 | CCTCGCCCTGGCCAC[C/T]GAAACCGTGGACATG | 10277 |
rs184369454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088663 | GGTGTGAGCCACCAC[A/G]CCTGACCGTATTTTA | 10277 |
rs184372476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146559 | TAGGAATTCCATCCT[C/T]AGTGGCCAGCATTTT | 10277 |
rs184374444 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105236 | AAACTTTTAATTTTG[G/T]AATAGTTTCAGTTAG | 10277 |
rs184380088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100850 | TGAGCCACTGCACTC[A/G]GCCAATGATATACTT | 10277 |
rs184388610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122620 | GTGAAAATGCAGATA[C/T]GTAGTGCTTAAAAAT | 10277 |
rs184394520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10140018 | GAGCCACTGCACCCG[A/G]CCCATTTTAATTGGC | 10277 |
rs184431896 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167182 | CGGTGGCTTACGCCT[A/G]TAATCCCAACACTTC | 10277 |
rs184444766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117416 | ACTCTGCCAAAAATA[A/T]TCAAGAGATAAGAAT | 10277 |
rs184454398 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139207 | TGGATGCTAGCCTGG[A/C]CAACATAGTGAAAAC | 10277 |
rs184471942 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10061870 | TGTTGCTATACGTGT[C/G]TAGTGTGTGCTGATC | 10277 |
rs184474152 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082328 | ACATAGCGAGACGTT[A/G]CCTCTACAAAAAAAA | 10277 |
rs184476238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052892 | GGTGCTAAGAGATTT[A/G]GTTTCTTGAGAGCCA | 10277 |
rs184483344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100547 | AACCTACTTTAATGA[C/T]ATACTTTTATTTATT | 10277 |
rs184497465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10178264 | TGCCAGGGCACAGTG[C/T]CCCCCAAGGACTGAA | 10277 |
rs184506793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062815 | TACAAAATTAGCCGG[G/T]TGTGGTGGCACATGC | 10277 |
rs184509926 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160493 | GGAGTCAGCATTTGC[A/T]GGTTTTCCATGGTGT | 10277 |
rs184514434 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10118121 | AAGTTGCAAGGCTGG[A/G]CTTAAACTCAGTAAG | 10277 |
rs184560558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10044237 | TTTTGTATTTTTAGC[A/G]GAGACGGGGTTTTAC | 10277 |
rs184564921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10129563 | ACATTTAGGTGTAGG[C/T]GGAGGTAACGTGTCT | 10277 |
rs184567055 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10084208 | AAGGCACAGGGGCAA[A/C]TACTGTGTGTGAGAG | 10277 |
rs184567925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087622 | GTGGGTTTTGGGGAA[G/T]ATTATGTCACACAGG | 10277 |
rs184569141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10101735 | GGATGGTCTTGATCT[A/G]TTGACCTTATGATCC | 10277 |
rs184592009 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10171939 | AAGAGCAGGTTTGGC[A/G]CTCTGAGCCCTCTCC | 10277 |
rs184598641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150316 | AAAAACCAACCTTGG[A/G]ATTTAAGCAACTCAA | 10277 |
rs184606440 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10109252 | AAATCATAGAAATGC[A/G]TTCAGACTTGAGCAT | 10277 |
rs184639928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121575 | ATATTTTCATCTTTT[A/G]TAGAGACAGAGTCTT | 10277 |
rs184642616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039820 | GGGAGTAAAGGGTAG[C/T]TTGGGAGAAGGTGGC | 10277 |
rs184655805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10083712 | CTACTGAGTTCAGGA[A/G]GCTCCTAGAAGAGGT | 10277 |
rs184699151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10065339 | TTATGGGGCAAGTGG[C/T]GGGAGGAGCATGCGG | 10277 |
rs184718487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10056229 | TTCACAATTAGATGA[C/T]ACGTGAGATGCTTTT | 10277 |
rs184720557 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035933 | TGTTTTTAGTAGAGA[A/C]GGGGTTTCACCGTGT | 10277 |
rs184730461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10145303 | TGATTCTCAGTTTAA[C/T]ATCACCTCCCTTGGC | 10277 |
rs184776525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104623 | TTCTGATTTTACTTA[C/T]TAACTCTGCTAATGG | 10277 |
rs184840810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039603 | CCCTGCTGATTTTTT[C/T]TTTTTTTTGTATTTT | 10277 |
rs185082732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074157 | AACCTAGGCAGGGAA[C/T]CTCCATCAGCCTCAG | 10277 |
rs185093635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10109739 | CACTGCAACCTCCAC[C/T]TCCTGGGTTTAAGCA | 10277 |
rs185128283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150662 | GTCAAAAGATCAAGA[A/C]CATCCTGGCCAACAT | 10277 |
rs185168785 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181002 | CAAACACAGCCACAC[A/G]CGCACACAAGTATAA | 10277 |
rs185202559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10092932 | GTTGCAGAATTGCCC[A/C]ACTTGATCCGAAATG | 10277 |
rs185205044 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10134437 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGT | 10277 |
rs185219732 | snp | A/C/T | 0.0364654 | 0.130094 | intron-variant | UBE4B | GRCh38.p7 | 1:10175461 | TCGAGACCGTCCTGG[A/C/T]TAACACGGTGAAACC | 10277 |
rs185265971 | snp | C/G | 0.00547694 | 0.052043 | intron-variant | UBE4B | GRCh38.p7 | 1:10106623 | ATGTGTGTTTGCGGT[C/G]CAGGGAAAGGAGATT | 10277 |
rs185266660 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10130112 | AGAGTCTCACTCTGT[C/G]ACCCAGGCTGGAGCG | 10277 |
rs185275745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125500 | CTTTGTCATCCAGGG[C/T]ACCTGTGTTTTATAC | 10277 |
rs185283937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172187 | TGTGTGCTTCATTTC[C/T]ACAGCCACCGATTTA | 10277 |
rs185291882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157055 | GAGTCTTGCTTTGTC[G/T]CCCAGGCTGGAGTGC | 10277 |
rs185294800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10048470 | AGTGAGCATAAATGC[A/G]GAAGACAAGAGGACT | 10277 |
rs185298917 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10070388 | TTGTAAGTATACAAC[A/C]CAGTGAGTTTTCATA | 10277 |
rs185302867 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089738 | GGAGTCTCACTCTGT[C/T]TTCCATCCTGGAGGG | 10277 |
rs185307265 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10136067 | GCAGGGAAACGGCTC[C/T]GGAATCAGTAGTTTA | 10277 |
rs185312844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114600 | CAGGTGCTGTGGCTC[A/C]CACCTGTAATCCCAG | 10277 |
rs185317380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110668 | TTTGGTGGTTTTGTG[C/T]TTGTTTTTTAACTGT | 10277 |
rs185323658 | snp | A/G | 0.0164848 | 0.0892785 | intron-variant | UBE4B | GRCh38.p7 | 1:10130487 | TTGACTGGCTCTTCC[A/G]TCTTCTGCCTAGGTT | 10277 |
rs185332003 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10096261 | TACCCTATTTGCTTC[A/G]TACGGATCAAGGTGT | 10277 |
rs185341681 | snp | A/G | 0.0001729 | 0.00929623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151279 | CAAGATGAGTTTCTC[A/G]GCAGTTTCTCAGCGG | 10277 |
rs185342978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058678 | CCTGCAGGTGGGCAA[A/G]GGTGCCTGGCACCTG | 10277 |
rs185346063 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10053536 | CAAGTTCTGGGGTAT[A/G]TGGGCTGGATGTGTA | 10277 |
rs185360913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093685 | TCTCTGTTTTCTTTT[C/T]TCATACTTTTTTTTT | 10277 |
rs185390267 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10052067 | AGATGTCTAATAGTG[G/T]CATTTTTTTTTTTTT | 10277 |
rs185425540 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10118482 | AGCTGGGATTACAGG[C/G]ACCTGCCACCACACC | 10277 |
rs185439869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092551 | AAAATAAGGAGGCCA[G/T]GCACCGTGGCTTATG | 10277 |
rs185448690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076350 | CCTGGTTTTAAGCAA[C/T]TCTCCTGCCTCAGCC | 10277 |
rs185457994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047322 | CATGCCTGCTAGGGG[A/G]CCAGACTCATGCTGT | 10277 |
rs185483111 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031380 | CTGCGCCCAGCCCGG[G/T]AGTGACTGTTAATGG | 10277 |
rs185567251 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072918 | AACTGCATTGATCAT[A/C]ATATCATCTAATAAT | 10277 |
rs185575848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136902 | TTCTGCCTGGGTGAC[A/G]AGAGCAAAAGTCCAT | 10277 |
rs185600572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079575 | TATGCTTCTTTATTA[A/C]TGATTTAAATGAAAG | 10277 |
rs185602325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10176494 | TCCATTCTTTTTCAT[C/T]TTTTTTCTTTGGTTT | 10277 |
rs185604586 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099590 | TTTGGTCAAAATCCC[A/G]GGAGGGTTTTTAAGG | 10277 |
rs185606226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159188 | AACAATTAGGTCAGA[C/G]TTGTCATTTAAAGTA | 10277 |
rs185613834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10116212 | CAGTGGCATGATCTC[A/G]GATCACTGCAACAAC | 10277 |
rs185667991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160921 | GCATTCCAGGCTGGG[C/T]GACAGAGTGAGACCC | 10277 |
rs185790354 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180027 | AAGCAGCGGCCGCAG[C/T]GAAGCTGCCGTTCAT | 10277 |
rs185813403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140546 | ATAAAAAATTCAAAC[A/T]ATGATTGTGGATTTA | 10277 |
rs185824684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140783 | TTGGGGTGTGTATAT[A/G]CGTATTGGAAAGAGG | 10277 |
rs185845233 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180305 | TCATGAATTTTTTTT[A/T]AATCCAATATCCGTT | 10277 |
rs185845402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084686 | TTCCTTTTTTTCTTT[C/G]TTTCTTTTCTTTTTT | 10277 |
rs185849179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054268 | CAGTAAGCCACCTCA[C/T]ATCTTTCAGCAAGAA | 10277 |
rs185853434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161760 | TAGAAAAGAGGCCTG[C/G]CTTGCCAGGTTCCAT | 10277 |
rs185857246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101914 | AGTCGCAAGTAGAAG[A/G]TTTTGGAAAACATGA | 10277 |
rs185861981 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10036880 | TTTAGGAAATTAGGT[A/G]AGGCAGAGTTTCATA | 10277 |
rs185865465 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10118773 | CCTCCCAAAGTGCTG[G/T]GATTACAAGTGTGAA | 10277 |
rs185865531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075066 | ACAATTCATGTTTTC[C/T]AGACCTGGATTGGCA | 10277 |
rs185868380 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077342 | GTGTGTCTGTGTCCA[A/C]ATTTCCCTCTTATGA | 10277 |
rs185903925 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10037110 | TTGGCTCATTGCAAC[C/T]TCTGCCTCCCGGGTT | 10277 |
rs185908205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057537 | TTCTCCTGCCTGAGC[C/G]TCCTGAGTAGGCACA | 10277 |
rs185908972 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10168821 | GGCGTGAACCCGGGA[A/G]GCAGAGCTGGCAGTG | 10277 |
rs185909811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078350 | GTAGGGCTTACTGCA[A/G]GTCAGACACAGTACT | 10277 |
rs185936572 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10147943 | ATTTAAAATATGTGT[A/G]TAGGCCGGGTGCGGT | 10277 |
rs185943129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115499 | TGGTCTCCAACTCCT[A/G]TACCTCAAGTGATCC | 10277 |
rs185960348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064414 | TTGTAGTATTTCTAT[A/G]CATACGTGCAGTAAG | 10277 |
rs185976631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102546 | CTCCCAAGTAGCTCC[A/G]AGTAGCCAGGCCCGC | 10277 |
rs185993354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10056967 | TACAGGCATGTGCCA[C/T]CACACCTGGCTCATT | 10277 |
rs186017611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10142277 | ACTCTTGTGATACCC[A/G]TAGCCATATAGGTCA | 10277 |
rs186025734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10173206 | ACTGCTGGCCGAGCG[C/T]GGTGGCTCATGCCTG | 10277 |
rs186064002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097370 | AAAAAAGACAACAGG[C/G]GTCCAGGATATATCT | 10277 |
rs186091934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085720 | AACAAGTACAGAGTT[C/G]ACTAACAGCGTGCAT | 10277 |
rs186135359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042272 | ACGGTTCATTCAACA[A/G]CGCTTACAGTTGACT | 10277 |
rs186136420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040490 | TCCTGGGCTCAAGTG[A/G]TCTGCCCACCTCAGC | 10277 |
rs186141498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162904 | TTCTACCCATTCTCT[A/G]AGTAAGGTCCTATCC | 10277 |
rs186148561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10063066 | TGAGGTCAGGAATTC[A/G]AAACCAGCCTGGCCA | 10277 |
rs186161961 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119176 | GTGAGCCACCGTGCC[A/C/G]GGCCCAGGCTAGTCT | 10277 |
rs186181900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126323 | TAGATAGATAGATAG[A/T]TAGATAGATAGATAG | 10277 |
rs186218419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10089102 | ACCTCTGCCTCCCAG[A/G]TTCCAGTGATTCTGC | 10277 |
rs186241305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048155 | CATCCGTCCTGAATG[A/C]GTTTTGGGAGGCAAC | 10277 |
rs186357077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069096 | TTTCTTCAACCGCAT[A/G]TTATAGTGAGTCAGA | 10277 |
rs186357325 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10038163 | CACATGCCTGTGATC[C/T]GAGGTACTCAGGAGG | 10277 |
rs186470422 | snp | C/G | 3.78451e-05 | 0.00434984 | intron-variant | UBE4B | GRCh38.p7 | 1:10168310 | TTGGTGGTTTGGACT[C/G]CACATTCAGACTCTC | 10277 |
rs186489452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171592 | GGGTGAGAGAGTGAG[A/G]TCCTGTCTCAAAAAC | 10277 |
rs186491695 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10124600 | TCTAGAGAGGAATGA[A/T]AACTGGGATGGAGCT | 10277 |
rs186492230 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10092368 | TAGCTGGGACTACAG[C/G]TGCATGCCGCCACGC | 10277 |
rs186504798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10149758 | CAAATTAACATTTTA[C/T]TTCTAAAACATTACA | 10277 |
rs186504991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108528 | CTCATTGTCTTACAA[C/T]TTTGCTCTTAAATTG | 10277 |
rs186516177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128343 | ATGCTTGCATAATAA[C/T]GAGGACACAGTGAGT | 10277 |
rs186516224 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10177023 | CGATCTCCTGACCTC[A/G]TGATCTGCCTGCCTT | 10277 |
rs186543231 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10173439 | GTGAGCGGAGATCGA[A/G]CCACTGCACTCCAGC | 10277 |
rs186548932 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131521 | AAGTTACAGGCTTGG[A/G]TAACTAAGGTAATTT | 10277 |
rs186551277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154472 | CTTGAAATTTATTCA[A/G]TGGAAATAATTACGA | 10277 |
rs186553338 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10153561 | CACAGTAGCTTACAC[C/T]TGTAATCCCAGCACT | 10277 |
rs186629095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051502 | GGTAGCAAATAGACC[A/G]TGGCTTATGTGAAAG | 10277 |
rs186629176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10072376 | CAATGTGTTGTGTTA[C/T]CGCTTTTTTTTTTAT | 10277 |
rs186672580 | snp | A/C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041532 | TAGAGATGGGGTTTC[A/C/T]CCAAGTTGGCCAGGC | 10277 |
rs186673057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055071 | GATTACAGGTGTGAG[C/T]CACCGCACCCGGCGT | 10277 |
rs186675774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147209 | AAGAATTCACTTCTC[C/T]GCAAGGCGCAGTGGT | 10277 |
rs186698521 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10133211 | CTTGACTAGTAATAA[A/T]TAATGAATGAATGAT | 10277 |
rs186717022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112047 | GAAGAAACTGAAACA[A/G]AGTCGCTTTAAGAGC | 10277 |
rs186720383 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10044751 | CATGCCCGGCTAATT[G/T]TTTGTATTTTTGATA | 10277 |
rs186722221 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174874 | AGTGCAGAAGGATGG[A/G]TGGTTGGCAAGCACT | 10277 |
rs186724464 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075738 | CAAACAGAAAATCTC[A/T]CTTAAGACAGGTTAC | 10277 |
rs186724764 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094555 | TCTCCTGCCTCAGCC[A/T]CCTGAGTAGCTGGGA | 10277 |
rs186732501 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155173 | ACGAGTGCTGGGCCT[A/G]GTGGAGTCCTGCTGG | 10277 |
rs186733958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113509 | ACAAGAAAAGCAATC[A/G]TCTACATAGTCTTCT | 10277 |
rs186765435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098858 | TAAGAACAAGGATGA[C/G]TGCTATTTCTTCTTG | 10277 |
rs186778425 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174469 | ACTTTGGGGAGCCGA[A/G]GCGGGCAGATCACCT | 10277 |
rs186780695 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10136711 | GATTGCCTGAGGTCA[A/G]GAGTTCGAGACCAGT | 10277 |
rs186810308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175852 | GTAAGATTAATATAT[A/G]ACGTAGAAGTAACCA | 10277 |
rs186886787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063295 | AAACAAAACAGATGT[C/T]GGCAACCTGTAGGAC | 10277 |
rs186916931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094131 | AAAGTAATTTTTAAA[A/G]TTTCAATGTAAAACA | 10277 |
rs186939520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131996 | CTAGCTGGGTGTGGC[A/G]GCGTGTGCCTGTAAT | 10277 |
rs186985399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116056 | TAAAACATGTCAATT[C/T]CTCTTGGTCCTGTTA | 10277 |
rs187031332 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10053770 | CACGGCTCACTTGCA[A/G]CCTCGACCTTTCGGG | 10277 |
rs187033730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158746 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10277 |
rs187058781 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093875 | AATTTTTGTATTTTA[A/G]CTAGAAACAGGGTTT | 10277 |
rs187140286 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10051136 | CTCAGCCTCCTGAAT[A/G]GCTGGGACTACAGGC | 10277 |
rs187244016 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10074832 | ATTCTCTTACTGTTG[C/T]CATCCAGTGTCCTGG | 10277 |
rs187266696 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032120 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCGCCCG | 10277 |
rs187330806 | snp | A/C | 0.00358891 | 0.0422285 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100711 | AGGCATGTGCCACCA[A/C]GCCTGACTAATTTTA | 10277 |
rs187338263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117826 | GCCAAGGTTTGAACC[G/T]AGATGGCCTGGCTTC | 10277 |
rs187340094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178346 | TGCTAGCTGTAAAAA[G/T]TCAAAAAAAAAGCCC | 10277 |
rs187342139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139718 | TTTCTGCTTTTATTT[A/G]TTTATTTTAGTTTTT | 10277 |
rs187345168 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10160598 | ACTGTCATCAGCCGT[G/T]CAAGGTGGCTCCAAA | 10277 |
rs187350685 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144797 | CTATGATTTGCCGCT[C/G]GTTGTAAGATATACT | 10277 |
rs187355549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10033712 | GAGGAGGTTGGGGGA[C/T]ACCTTGAGGGATTAG | 10277 |
rs187378947 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10104025 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCT | 10277 |
rs187382225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121438 | TTTTAAGAGACAGAA[C/T]CTCACTCTGTTGTCT | 10277 |
rs187389231 | snp | A/G | 0.0103365 | 0.0712171 | intron-variant | UBE4B | GRCh38.p7 | 1:10165422 | ACTGCTTGGTCTTCA[A/G]CCTCCACTCTTGAGC | 10277 |
rs187437430 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10159433 | ATCCCAGCACTTTGG[A/G]AGGCCGAGCAGGGCG | 10277 |
rs187452088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116402 | CCTGCCTTGGTGTAC[G/T]AAAGTGCTGGGATTA | 10277 |
rs187525463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039111 | ACAAACAAAAAAGCA[A/C]TTATAATTAAATTTG | 10277 |
rs187566373 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10080633 | TGCAGCATTATTCCA[A/G]ATAGCCAAGATATGG | 10277 |
rs187584073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061168 | GAATTTGTAGTACTG[A/G]AATCCACCCTTTAAT | 10277 |
rs187585530 | snp | A/G | 0.00215834 | 0.0327798 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107367 | TCTTGTGTCCAGTTT[A/G]GGTCCAGGTATCAGA | 10277 |
rs187591479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038653 | CTTTTGTATCAACAT[A/C]CTACGTAACACTGAC | 10277 |
rs187595495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10081311 | ATGATCTGCCCACCT[C/T]GGTCTCCCAAAGTGC | 10277 |
rs187597003 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100280 | AGGTGTGAGCCATCG[C/T]GCCTGGCCTATTTTC | 10277 |
rs187597204 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UBE4B | GRCh38.p7 | 1:10035097 | TCCGCCTCCCGGGTT[C/T]ACACCATTCTCCTGC | 10277 |
rs187609127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111442 | CCGGCTCCCTCACTC[C/T]CCTCAGGTCTATCAG | 10277 |
rs187644453 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10104817 | CAAGTGTCTTACACA[A/T]GTTAAGTGGCAACTC | 10277 |
rs187671475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065547 | TTAAATGTGAACACA[A/T]TTGAATGTGTCACCG | 10277 |
rs187710609 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10137329 | GTTATATAGTGTTCT[C/G]TCTGCCTCCACCGCC | 10277 |
rs187759271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042762 | TATTTCTGTGGCCTA[C/T]AGGTACAGAGAACAA | 10277 |
rs187835568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100021 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 10277 |
rs187861109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060723 | GAGGTTCATTTTGCT[G/T]TGTATTTTAGAATCC | 10277 |
rs187907236 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10175365 | CTTAGAAAATAAAAA[A/G]AAATAGCCGGGTGCA | 10277 |
rs187915647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156939 | TTTGGAAGGACGATG[G/T]AGGAGGATCGCTTGA | 10277 |
rs187933915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122267 | TGTGCCCATTTCAAC[A/G]AATCAGTCAAACATC | 10277 |
rs187963126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087723 | CATCATCACATGCTT[A/G]AGTTAGTGCTGGCCG | 10277 |
rs187999050 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120736 | CCAACTACTGGGGAG[G/T]CTGAGGCACGAGAAT | 10277 |
rs188029568 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10064976 | ACCATGTTGACCAGA[C/G]TGGTCTTGAACTCCT | 10277 |
rs188034006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086367 | CCCGCCTTGGCCTCC[C/G]AAAGTGTTCAGTGAC | 10277 |
rs188039438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103310 | TCCATGATTTCTATA[A/G]TACTATGTAAATAGG | 10277 |
rs188083955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091348 | AAAACAGTGATATTT[C/T]GTACTATTGATTTGA | 10277 |
rs188098685 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10127213 | TACTTAAAAAAAAAA[A/C]ACCTATTAAAAATGC | 10277 |
rs188107283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074707 | TTTCATGCATTCTCT[A/G]TATCTGTTCCTTCTT | 10277 |
rs188113224 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093689 | TGTTTTCTTTTTTCA[G/T]ACTTTTTTTTTTCTT | 10277 |
rs188141589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170976 | TGGGGAGTAAAGTTG[A/G]AATATAATGTTGTCT | 10277 |
rs188143017 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10152025 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 10277 |
rs188166092 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111032 | TGTCTCTCTCTGTCT[C/T]TCTCTGTCTCTGACA | 10277 |
rs188178045 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE4B | GRCh38.p7 | 1:10173343 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 10277 |
rs188178443 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10166186 | AACAAGAAAAGGCCT[A/C]TGAACAGATGTAAGA | 10277 |
rs188206438 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157350 | ACGCGTGGTGGATAC[A/T]CCTCCAGTCCCAGCT | 10277 |
rs188337770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043720 | GGCGTGATCCAACGC[A/G]CTGGGCCGGGATGCT | 10277 |
rs188350800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086850 | ATGTGCCACCACGCC[C/T]GGCTAATTTTTGTAA | 10277 |
rs188351552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076965 | TTGGCCAGGCTGGTC[C/T]CGAACTCCTGACCTC | 10277 |
rs188355187 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10096915 | GTGGTGTTGCATGCC[C/T]GTAGTACCAGCTACT | 10277 |
rs188375522 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108186 | GCGTGCTCCCTTCCC[A/C]CCCCCTCCCAGCCTC | 10277 |
rs188395908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10070764 | GCTCTTTAATTATAT[C/G]TTAAAAGGAAGAAGT | 10277 |
rs188402535 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10071517 | TACTTGAGCCCAGGA[G/T]TTCAAGGCTGCAGTG | 10277 |
rs188435192 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10148851 | AGGCTGAGACATGAT[A/T]ATCGATTGAACTGGG | 10277 |
rs188438172 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10138082 | TGGGATTACAGATGT[A/G]CACCACCACGCCTGG | 10277 |
rs188532332 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBE4B | GRCh38.p7 | 1:10175467 | CCGTCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 10277 |
rs188613065 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10115232 | CTCAAGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 10277 |
rs188617016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10065131 | TTTATTTTTTGTTAC[A/G]TTCACTTTGTCTGTA | 10277 |
rs188619406 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10135477 | GGCATGGTGGCACAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs188627620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157763 | GCCTGGCGACAGAGC[A/G]GGACTCTGTCTCAAA | 10277 |
rs188670748 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10049245 | GTGGAGATGCTGCTC[A/G]AATATGACGAAGACC | 10277 |
rs188678304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090997 | CCACATAGAATGCAT[A/G]ATTTCCTTTAGCAAA | 10277 |
rs188691586 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10177985 | TTTGTCTGGGTCCAC[G/T]GTGGGCGCCTGACCT | 10277 |
rs188712428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116979 | GGAGAGTTTCTTAAC[C/T]TTTGGTTCTATTGCC | 10277 |
rs188736199 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10160154 | AAGCTATTTCAGTTC[A/G]CCAGCAAGTTCTCAT | 10277 |
rs188789634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10082891 | TCAACTCCCATTTAT[A/G]AGTGAGAATGTGCAG | 10277 |
rs188791705 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10053128 | ACAGGTGTTTACAAC[C/T]GTGCATGGCTTTTAT | 10277 |
rs188796835 | snp | G/T | 0.00125831 | 0.0250514 | intron-variant | UBE4B | GRCh38.p7 | 1:10168296 | ACCCGGGGCTCTGTT[G/T]GGTGGTTTGGACTCC | 10277 |
rs188806458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10146747 | TTAACTGTGTGCTAG[A/G]CCTGGTGGTACTCGG | 10277 |
rs188818757 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124368 | AGTTTTGTCATGTTG[G/T]CCAGGCTGGTCTTGA | 10277 |
rs188858855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074262 | GCTTGGACCCTAGAT[A/C]CCATCTCCCTTCAGT | 10277 |
rs188892553 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10095810 | AGAGTTTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 10277 |
rs188903405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10056240 | ATGACACGTGAGATG[C/T]TTTTTAGTGCTTTTG | 10277 |
rs188907544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076392 | TGGATTACAGGTGCC[C/T]ACCACCATGCCTAGC | 10277 |
rs188920063 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10096322 | GCCAAAAATGGGTGG[G/T]AAGAGTGGCTGAGGT | 10277 |
rs188923366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055800 | TAGCACGTGCCCGTA[C/G]TCCCAGCTACTTGGG | 10277 |
rs188948806 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10164343 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAGAAAA | 10277 |
rs188989299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118262 | GTTAGTTTCATATTT[A/G]TAAAGGGCCTTCTTT | 10277 |
rs188990604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040919 | GCCACCGCACCCAGC[A/C]TAACATCCCCACCTC | 10277 |
rs189000482 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10063136 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAGTCC | 10277 |
rs189011013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039851 | TGCAGACTGCAAGAC[A/G]TATTAGGAGGCTGTT | 10277 |
rs189019024 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10083808 | CATGGGTACTTCCTC[A/G/T]AATTGGACTGGCCTT | 10277 |
rs189040623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160741 | CGCTTGAGCCCAGGA[A/G]TTTGAGACCAGCCCT | 10277 |
rs189047240 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE4B | GRCh38.p7 | 1:10035945 | AGACGGGGTTTCACC[A/G]TGTTAGCCCAGGATG | 10277 |
rs189156930 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10076189 | GTAGATTTATTATCC[A/C]CCGAATGTGATTGAG | 10277 |
rs189180764 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10113901 | GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAT | 10277 |
rs189190596 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10142658 | CCTGGGAGACAGAGC[A/G]AGACTGTCTCAAAAA | 10277 |
rs189201045 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10035720 | CAGAGATAGTTTTTT[A/T]ATTTTTTTTTATTTT | 10277 |
rs189230799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140551 | AAATTCAAACTATGA[A/T]TGTGGATTTATCTGT | 10277 |
rs189232771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172022 | TTTCTGAAAAGAGCC[C/T]GGTTTCTCAAGGGAT | 10277 |
rs189240629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150590 | CTGTAGGCTGGGTGC[A/G]ATGGCTCATGCCTGT | 10277 |
rs189256388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084345 | CAATTATAATCTAAT[C/G]CGAGGGCTTGCAAGG | 10277 |
rs189261680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10101791 | GGATTACAGGCGTGA[A/G]CCACTGCGCCTGGCC | 10277 |
rs189262553 | snp | A/G | 0.00676381 | 0.0577595 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10101207 | TAAGGTTGGTAAGCG[A/G]TGAAGCCCTTGGTAC | 10277 |
rs189263292 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036436 | AGGGCTGGTTCAATA[A/C]CTGTTAATTTTACTC | 10277 |
rs189269517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118609 | TCCTGGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 10277 |
rs189281760 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140168 | GTTATATCATATCTT[A/G]TTACTCAGTTCAAAA | 10277 |
rs189313737 | snp | C/T | 0.000234486 | 0.0108253 | intron-variant | UBE4B | GRCh38.p7 | 1:10179411 | GCTTTGCTTTGTCCC[C/T]GCAGACCCTCTGATG | 10277 |
rs189427964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046187 | CTCACTGGCTGGAAC[C/G]CAAGTCACATGGCCA | 10277 |
rs189443257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10067173 | ATGGCCTTCACTGTT[C/T]TGAATCTATTTTTAG | 10277 |
rs189476537 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10175645 | GACAGAGCGAGACTC[C/T]GTCTCAAATAAATAA | 10277 |
rs189496332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10088461 | TCTCACTGCAACTTC[C/T]GCCTCCCGGGTTCAA | 10277 |
rs189505780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10147301 | AGTTCAAGACCAGCC[C/T]GGCCAACATGGCGAA | 10277 |
rs189510926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105122 | CAGTTGCATTTGTAG[C/T]ATAATAAAGTAACCT | 10277 |
rs189515262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145993 | TGAACAGTAGGATAA[A/T]ATGTGGAAAGTTTAC | 10277 |
rs189517928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056713 | TGGGATCCTGGCCAG[C/T]GCTAGCTACGCGATT | 10277 |
rs189519290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123142 | CTCAGGAAAATAAAT[C/T]ACTGTCGGCCGGGCG | 10277 |
rs189596472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172228 | TCCCTGCGTGATCTT[C/G]TAGTCATCCCATAAA | 10277 |
rs189661770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053579 | AGGTAAGCGTGTACC[A/G]TGGTGGTTTGCTGCA | 10277 |
rs189665785 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10042320 | CAGACAAACGTTGCT[A/G]TATGGAGCTTCGTCC | 10277 |
rs189700711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062204 | TGAGCCACCACACCC[A/G]GCCCTATTTTTTCTA | 10277 |
rs189751135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10130443 | GAGAGTTTTCATTAC[A/G]TTTTTACCCCACCGG | 10277 |
rs189773342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168584 | CATTATTGATTCCTA[C/T]ATTTTACTTATAGAA | 10277 |
rs189781158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10093385 | AAGTTTTACTGTATT[C/T]TGTGAACTTGTTTCA | 10277 |
rs189794554 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114733 | GCTGTACATGGTGGC[A/G]AGCGCCTGTAGTCCC | 10277 |
rs189798500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10088741 | CTGGGGGACAGTGAC[A/G]CAATCATGGCTCACT | 10277 |
rs189817398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175075 | CAAGAGTAGGCTGAA[A/G]ACCCATGTCCAGAAG | 10277 |
rs189839095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047470 | CCCATAAGAGCATGG[A/C]CAGAAAGCTTCATAT | 10277 |
rs189912674 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10048268 | ATTGAAAGAGAAGAT[A/T]GGGAGGGAGACGTTA | 10277 |
rs189951838 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039668 | TGGTTTCAAACTCCT[C/G]ACCTCAAGTGGCCCA | 10277 |
rs189995977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109946 | TCAGGTGGTCCGCCC[A/C]CCTCGGCCTCCCAAA | 10277 |
rs190026194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099659 | AAAGAGCCAAGGATA[A/G]CAAAACCTCTTAAAG | 10277 |
rs190027098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150761 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCGC | 10277 |
rs190031543 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116238 | ACAACCTCCTCCCAC[A/C/G]GTCAAGTGATTCTTG | 10277 |
rs190040770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073773 | ATCACAAACTCGGGT[A/G]GACCCTTGATACTGG | 10277 |
rs190047740 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068270 | CTGACATGAAGTGAT[C/G]CCACCTACCTTGGCC | 10277 |
rs190054069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134505 | CAACAAGAGTGGAAC[C/T]CCATCTCAAAAAAAA | 10277 |
rs190056567 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176844 | AGGCTGGAGTGCAGT[A/G]GTGCGATCTCAGCCT | 10277 |
rs190057878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109378 | TGTTTTTGCTGCCGA[A/G]AGTCTGTGCATCTAC | 10277 |
rs190059410 | snp | C/T | 0.00130763 | 0.0255364 | intron-variant | UBE4B | GRCh38.p7 | 1:10105474 | TGTGTAACCTGTGTT[C/T]GAACTGTGTGTAACC | 10277 |
rs190066865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159315 | CATCTAAATTATCTG[C/T]CAGTGCCTAAAAACA | 10277 |
rs190087537 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10136916 | CGAGAGCAAAAGTCC[A/C]TCTCAAATAAATAAA | 10277 |
rs190115449 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161916 | TATTGATTCTGTTCT[A/T]GGAATTGTCAGGCTC | 10277 |
rs190132299 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094394 | TTGAGAGAATTTTGC[A/C]GGGAACACCCGTATA | 10277 |
rs190136711 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10141992 | ACAGTCTTAGAAACT[C/G]CTGATTAATTCACAT | 10277 |
rs190142704 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10112345 | TCATGAATTTTGTAC[A/G]GCTGAGGGAAAATAT | 10277 |
rs190150965 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180318 | TTTAATCCAATATCC[A/G]TTGATTTGATTGTGA | 10277 |
rs190172050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10069199 | GTTTAAGGTGACTTC[A/G]TATTTTTTCCAACAA | 10277 |
rs190266680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10034702 | TGATTGTACTACAAG[A/G]CTTCCATGCTCCAGT | 10277 |
rs190273140 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10054346 | CAATTAAAATTTGCT[G/T]TAAATAGTTCTTTGG | 10277 |
rs190274931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075234 | TAAAACTTCACTTAC[A/G]AAAACAGGCAGTAGC | 10277 |
rs190277227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119103 | GGCCAGGATGGCGTC[A/G]ATCTCCTGACCTTGT | 10277 |
rs190297247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092758 | GCTTGAACCTGGGAG[A/T]TGGAGGTTGCTTTGA | 10277 |
rs190304285 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10037284 | TGCCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 10277 |
rs190316525 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180097 | CCCAGAGCGAGCAAA[C/T]GCTGAGACCTGAAAG | 10277 |
rs190317568 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10057811 | CTTTGTAAGTATTTT[G/T]TGCTTTATTTTTGAG | 10277 |
rs190323498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078538 | TTTAGATGATTTGTG[A/G]TTGCTTAATCTTCAG | 10277 |
rs190325273 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10052241 | CTGGCTGATTTTTTA[A/G]TTTTTTTTTTTGTAG | 10277 |
rs190388284 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10099145 | TATTTGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 10277 |
rs190392436 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116155 | ATACTTTTTTTCTTT[G/T]ATTTTAGGACAGCGT | 10277 |
rs190535900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098217 | ATAGTATATCATGAT[A/C]AATTTAGGCTTACTT | 10277 |
rs190556379 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10136476 | GGTGACAGAGTAAGA[A/C]CCTCTTAAAAAAAAA | 10277 |
rs190565107 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10129655 | TTTCTATGATTTTTT[C/T]CCCTTTTTTTTCTAA | 10277 |
rs190568788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057074 | GCCTCAGCCTTCCAA[A/C]ATGCTGGGATTACAG | 10277 |
rs190573443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10167206 | ACACTTCGGGAGGCC[A/G]AGGCAGGCTGATCAC | 10277 |
rs190575851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160999 | GGTCCTTGAATTCCA[C/T]AGTGCCTGACTTGTG | 10277 |
rs190637482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119264 | AGGTGTGAGCCACCG[C/T]GCCTGGCCTCTAAGG | 10277 |
rs190656574 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10158563 | AAAGCATGCACAGCT[A/G]GGTTCTTGTTGACTG | 10277 |
rs190663754 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10162948 | GGTTTGTCTTCGCCA[A/G]TCAGCATAGCTGAAA | 10277 |
rs190752532 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10169476 | ATAAACAGATTTCAG[C/T]GCAAGAGCCATGGAA | 10277 |
rs190760290 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10148504 | AGGTGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 10277 |
rs190796124 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115777 | CCTAGGCTATGTGAT[A/G]TATAGCCTGTTTCTC | 10277 |
rs190819609 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10036931 | ATGATTATACAGTCC[A/G]TGAAAAAGGCTGGTA | 10277 |
rs190832240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077382 | GATTAGGGACCACCG[C/T]AATTGAGTATGAGCT | 10277 |
rs190876641 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031428 | TGGGATGATGAAAAT[A/G]TTCTGAAATTGGACA | 10277 |
rs190913331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064699 | TGTGTACTGCTGTAC[A/G]TGGCTAGAGAAAAAA | 10277 |
rs190923295 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10142430 | GTAATCCCAACACTG[A/G]GAGGCCGAGGTGGGC | 10277 |
rs190929970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10102559 | CCGAGTAGCCAGGCC[C/T]GCAACCGCGCCTGGC | 10277 |
rs190945212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10065043 | GCTGGGATTAAAGGT[A/G]TGAGCCACCGCGCCT | 10277 |
rs190947854 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10086385 | AGTGTTCAGTGACTA[G/T]TAAATATGCACTGTG | 10277 |
rs190992511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143595 | CACATCTACAACGTC[C/T]CTTTCGCCATGGGAG | 10277 |
rs191002648 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10174301 | CGGAGGCTGAGGCAG[A/G]AGAATAGCTTGAACC | 10277 |
rs191019319 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120831 | CAACAGAGCAAGACT[C/G]TCTCAAAAAATAATA | 10277 |
rs191032979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164782 | GCTCCAGCACTCAGC[A/C]CTTAGGCTTCAATTT | 10277 |
rs191040887 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | UBE4B | GRCh38.p7 | 1:10148132 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA | 10277 |
rs191060395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106811 | ATTGTGAATCCCTTT[C/T]TTCCCTTTGAGAGTT | 10277 |
rs191070947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125938 | TTTAAGTTTAATGTA[A/G]TAATAATGTTGATTG | 10277 |
rs191078815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10169043 | AGGTTAATGGGAGCC[A/G]GCCATCACTAGGGTT | 10277 |
rs191079638 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10079906 | TTAATAAATGGCTTC[G/T]GTCTGTTGGGCACTG | 10277 |
rs191138065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10045321 | GCCATGTCACATTTT[A/G]TAACTGAACATACAG | 10277 |
rs191138288 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10075812 | ATCATAATACTTTGG[A/G]AAGCCAAGGTGGGAG | 10277 |
rs191141435 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094675 | TCCTGACCTTGTGAT[C/T]CACCCGCCTCGACCT | 10277 |
rs191146821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10065888 | TAAAAAATAAATGGA[A/G]TCATTATGTGTACCC | 10277 |
rs191148302 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181449 | GGGGTAAGCTTTGTC[A/G]TATTCAGTCTTCTGC | 10277 |
rs191153235 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10113511 | AAGAAAAGCAATCGT[C/G]TACATAGTCTTCTAC | 10277 |
rs191192830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048644 | GTGGGGGAATGCTCA[A/G]CTGTGTCTAATGTTG | 10277 |
rs191193025 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070537 | CACCAAGGATAACCA[C/T]TATCCAAACTAATGG | 10277 |
rs191203933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090590 | TTTATTGAGGCGTTT[A/T]GGTTTTTTAAAAAAT | 10277 |
rs191216407 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UBE4B | GRCh38.p7 | 1:10174574 | GGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 10277 |
rs191232752 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10131999 | GCTGGGTGTGGCGGC[A/G]TGTGCCTGTAATCCC | 10277 |
rs191332176 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10124652 | TTACCTTTTTGTCTT[C/G]AAAGAGTGGCAAATG | 10277 |
rs191352204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10102306 | TGTTAACCTGGTCCT[A/G]TGGAATTCAGAAAAG | 10277 |
rs191366478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089110 | CTCCCAGGTTCCAGT[G/T]ATTCTGCTGCCTCAG | 10277 |
rs191370750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059407 | TGGAATGAAGAAATA[A/G]TTCCCCAGATCCAGG | 10277 |
rs191377862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063626 | AAGGTACATCTGGGC[C/T]GGGTGAGGTGGCTAA | 10277 |
rs191393291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155665 | TTAAAAGTTGCCACA[C/T]ACAAGATCAGTATGT | 10277 |
rs191408723 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | UBE4B | GRCh38.p7 | 1:10133212 | TTGACTAGTAATAAA[G/T]AATGAATGAATGATG | 10277 |
rs191410299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087737 | TGAGTTAGTGCTGGC[A/C]GTGTTTCTCCACTTA | 10277 |
rs191447805 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10126466 | AATTGAGTAGAGCAA[C/T]GACTCCTGGAGAGTT | 10277 |
rs191456265 | snp | A/T | 0.138546 | 0.223781 | intron-variant | UBE4B | GRCh38.p7 | 1:10049594 | TAAAAAAAAAAAAAA[A/T]TTTTTTAAATTAGGA | 10277 |
rs191463552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154488 | TGGAAATAATTACGA[A/G]TGTTTGTAAGTGATG | 10277 |
rs191470811 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10158899 | TCTGTTATCCTAGCT[A/G]CTTGGGAAGCTGAGG | 10277 |
rs191476969 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10091069 | TTGCTAATTCCTGTT[G/T]CCTGAAGCAGACATA | 10277 |
rs191581844 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10084842 | AGCTGGGATTACAAG[C/T]ACCCGCCACCATTCC | 10277 |
rs191582638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051140 | GCCTCCTGAATAGCT[A/G]GGACTACAGGCATGC | 10277 |
rs191622694 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10179198 | TCTTCTCTGTTCCCT[A/C/G]CCCCCAGCAGTAGCT | 10277 |
rs191623163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041586 | GCGATCCCCCCGCCT[C/T]GGCCTTCCAAAGTGC | 10277 |
rs191632085 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10160624 | CCAAATACCACTGGA[A/T]TGAGCTTATCATAAA | 10277 |
rs191654626 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10091515 | AGTGGTATGATTATA[A/G]CCCACTGCAGCTTCT | 10277 |
rs191681496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136801 | GCACACGCCTGTAAT[C/G]CCAGCTTACTAGGGA | 10277 |
rs191691081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107434 | TAGGAACTAACTTCT[A/T]TAAGCTCTAACAAGG | 10277 |
rs191718298 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175855 | AGATTAATATATAAC[G/T]TAGAAGTAACCATTT | 10277 |
rs191725910 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071096 | ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT | 10277 |
rs191745450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118071 | CAAATGACTCTCAGA[G/T]AGATTAAGTACTTGT | 10277 |
rs191756209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10139726 | TTTATTTATTTATTT[C/T]AGTTTTTGAGAGGAG | 10277 |
rs191783638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056392 | AAGACTATTTACTGT[A/G]TGTCAAGTAAACACT | 10277 |
rs191787729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076697 | TTGAGAAGCTGTAGG[C/G]GGTCCTTCCACTTCC | 10277 |
rs191802505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10096700 | GCACTCCAGCCTGGC[C/T]GATAGAGTGAGACTC | 10277 |
rs191805416 | snp | C/T | 3.30382e-05 | 0.00406423 | intron-variant | UBE4B | GRCh38.p7 | 1:10145047 | AGCTTAAGGTTTGTA[C/T]AGCTAAGTGGAATAA | 10277 |
rs191815928 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035947 | ACGGGGTTTCACCGT[A/G]TTAGCCCAGGATGGT | 10277 |
rs191838937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10165725 | TTCCCTCAGATTTTC[C/T]GACTCCTTCAGATAT | 10277 |
rs191848435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10114945 | TTGTCATGACTCTGG[C/T]GAGGGCTTTGTAGGT | 10277 |
rs191852646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10134577 | ATAATAATTATATAA[C/T]AGGCGGTATTCAACA | 10277 |
rs191891827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111509 | TAGAACACACACGCA[C/T]CCATGCACGCACACC | 10277 |
rs191914400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074834 | TCTCTTACTGTTGTC[A/C]TCCAGTGTCCTGGCT | 10277 |
rs191942675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10153671 | CTAAAAGTAAAAGGC[C/T]GGGCGTGGTGGCTCA | 10277 |
rs191974179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137882 | AACTGAATCATATTT[A/G]TATCTCTGTATCTAC | 10277 |
rs192005787 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10061838 | TGATGTTGAGGAGTG[C/T]TGTCAGTTACTTACT | 10277 |
rs192020252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10177685 | TATTTATAGTAAAAC[A/G]TATATGGCAAAAACA | 10277 |
rs192025563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10081368 | CCTGGCAAAACAACA[G/T]TATTATTACTTTATA | 10277 |
rs192030302 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100546 | TAACCTACTTTAATG[A/T]TATACTTTTATTTAT | 10277 |
rs192045403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039307 | CCTGGGAACTGGCTC[A/G]AAATTGGGGAGCTCA | 10277 |
rs192189455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093984 | ACAGGCGTGAGCCAT[C/T]GTGCCCAGCCAATGG | 10277 |
rs192205979 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131596 | AACTGCCGGCTGGGC[A/G/T]TGTTGGCTAATGCCT | 10277 |
rs192212607 | snp | A/T | 0.0573587 | 0.15934 | intron-variant | UBE4B | GRCh38.p7 | 1:10054073 | TATTAGATTTTTTTT[A/T]AAAAAAAAGACAGGA | 10277 |
rs192223291 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10055253 | TTGTGAAAATGTCTC[A/G]TAGGCCACCTTTTCA | 10277 |
rs192225984 | snp | C/G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172023 | TTCTGAAAAGAGCCC[C/G/T]GTTTCTCAAGGGATC | 10277 |
rs192290896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117358 | GTTTGTGCTTTGTTA[C/T]GTGTACAGGGATCCT | 10277 |
rs192292912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116403 | CTGCCTTGGTGTACG[A/T]AAGTGCTGGGATTAC | 10277 |
rs192296741 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10139188 | ATCACCTGAGGTCAG[G/T]AGTTGGATGCTAGCC | 10277 |
rs192305397 | snp | C/T | 0.0123084 | 0.0774772 | intron-variant | UBE4B | GRCh38.p7 | 1:10167474 | TAATAATAATAATAA[C/T]GACTAAGTAAAAGTT | 10277 |
rs192314115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146218 | GCACTTTGAGAGGCC[A/G]AGGCAGGCAGATCAC | 10277 |
rs192322708 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10159558 | GGCGCGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 10277 |
rs192461492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10166754 | CATGGCGAAACCCCA[A/G]TCTTTACCAAAAATA | 10277 |
rs192464754 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10122492 | GCTCATTGGCAGCCT[C/G]CATGCCATATAGAAT | 10277 |
rs192505814 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10092469 | ACCTCATGATCCGCC[C/T]GCCTCAGCTCCCAAA | 10277 |
rs192512361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108750 | ATATTTGTATTACGC[A/T]GAACATTTTATCACC | 10277 |
rs192542371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072749 | TTGATATCCAGGACT[A/G]TCTTTGTTGGGAAAT | 10277 |
rs192558957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171647 | AACACTTTGGGAGGT[C/T]GAGGCGGGCAGATCA | 10277 |
rs192567936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150131 | ATTGCTGTCATAAAA[A/G]CTGCCTTTAAAAAAA | 10277 |
rs192577994 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128964 | ATAGCTTATTAAATT[A/G]TAATTATTTATAGTC | 10277 |
rs192607494 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10035179 | ATTTTTTGTATTTTT[A/T]GTAGAGATGGGGTTT | 10277 |
rs192694792 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039697 | CACCTGCCTCTGCCT[C/G]CCAAAGTGCTGGGAT | 10277 |
rs192700387 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10108204 | CCCTCCCAGCCTCCA[C/G]CGCCCCCCTGTTCAC | 10277 |
rs192703044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149637 | ATATTTTGTACTAAA[A/G]TTTGTCTCAATTGTA | 10277 |
rs192704826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083398 | TTCCTTCTCCAATTT[C/T]GAGTCTTTAATGAAC | 10277 |
rs192708533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104569 | TCTGAGGAGGGAAAA[A/G]AAAAGTCCTTTGTAT | 10277 |
rs192730471 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10065214 | CTGAACTATTTGAAA[C/G]TATGGAGAACCACTA | 10277 |
rs192752497 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBE4B | GRCh38.p7 | 1:10175469 | GTCCTGGCTAACACG[A/G]TGAAACCCCATCTCT | 10277 |
rs192783703 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10104886 | TCAGATAAAATTTCC[A/G]TGAGTTAAAACTTTT | 10277 |
rs192788795 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10145685 | CTGTCTCCCACCCCT[C/T]GCCCCAACACTCATC | 10277 |
rs192888453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100753 | GAGATGGGGTTTCTC[C/G]ATGTTGGTCAGGCTG | 10277 |
rs192904636 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10062501 | TATTTTTAGTAGAGA[C/T]GAGGTTTTGCCATTT | 10277 |
rs192904996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171406 | GTGGCCAGGGAACTC[A/G]TCTGGTGTAAATGAA | 10277 |
rs192910764 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127347 | TCCCTGTTTCCTAAG[G/T]TCATATTTACTTGGG | 10277 |
rs192919145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121497 | CTCCTGGGCTCAGGC[A/C]GTCCTCCTGCCTCAG | 10277 |
rs192930494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044142 | CTGCCAGGTGCCAGG[C/T]TCAAGCGATTCTCGT | 10277 |
rs192934423 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097055 | AAAAAAAAAAAAAAA[A/T]AATAATAATAATAAT | 10277 |
rs192937367 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087518 | TGTTTTCATGATCTT[A/C]ACAGTTTTGAAGAAT | 10277 |
rs192938649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10157647 | GCAGGGCGTGGTGGC[A/G]CATGTCTATAGTCCC | 10277 |
rs192953287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160311 | ATAACTATATCAGTT[A/G]TTTTCTTATCTGTTG | 10277 |
rs192955317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10129796 | GCTGGGAATACAGGC[A/G]TGCATTACCATGCGA | 10277 |
rs192972996 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10092878 | AATGGAGTCCCCTGG[G/T]GTTTAGAGATTGAGG | 10277 |
rs193062848 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10035907 | CGCCACCACGCCCGG[C/T]TAATTTTTTGTGTTT | 10277 |
rs193093765 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076191 | AGATTTATTATCCAC[C/T]GAATGTGATTGAGAG | 10277 |
rs193096631 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10113968 | TGCTCAGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 10277 |
rs193105670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060938 | TTTTGTAGAGAAGTC[A/G]TCTTACTATGCTGCT | 10277 |
rs193188298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10150591 | TGTAGGCTGGGTGCA[A/G]TGGCTCATGCCTGTA | 10277 |
rs193190148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10178036 | CTGGGGACATAAATC[A/G]TGTCTGTTCCCAGGC | 10277 |
rs193191629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109702 | GTCACCCAAGCTGGA[C/G]TGCAGTGGAGCGATC | 10277 |
rs193209561 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | UBE4B | GRCh38.p7 | 1:10175377 | AAAAAAATAGCCGGG[C/T]GCAGTGGCTCACGCC | 10277 |
rs193233891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055980 | ATGCTTAGTCATCTA[C/T]GTTAATCTTGTCTGT | 10277 |
rs193243063 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10133697 | GGGAGGATCACTTGA[A/G]CCCAGGCATTTGAGA | 10277 |
rs193250408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10096163 | TAAATATAAAGTTGG[C/T]AAGCATATGCCTCTC | 10277 |
rs193265213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10051654 | CTGAATGTACTAAGA[A/G]GGTGAAGGTGGAGTG | 10277 |
rs199512231 | in-del | -/AAC | 0.0279329 | 0.114831 | intron-variant | UBE4B | GRCh38.p7 | 1:10073722 | AGATTCTGTCTCAAA[-/AAC]AACAACAACAACAAC | 10277 |
rs199515408 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080605 | CTGAAGAGATACCTC[-/T]ACTCATGTTCATTGC | 10277 |
rs199553452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152328 | AAATTTATTTCTTAA[A/G]TTGAAAATACCTGGT | 10277 |
rs199556580 | snp | A/G | 8.23608e-05 | 0.00641667 | intron-variant | UBE4B | GRCh38.p7 | 1:10130632 | GTAAGTATAGTGGCT[A/G]CTTGTACTTTGCTGC | 10277 |
rs199579279 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121222 | TTAGCCAGGCGTGGT[G/T]GCAGGCGCCTGTAGT | 10277 |
rs199629226 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148777 | AAACCCTGTCTCTAT[G/T]GAAAATACAAAAATT | 10277 |
rs199643842 | snp | C/T | 9.96926e-05 | 0.00705949 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106259 | TTCCCGTGATGGGCC[C/T]GTCTCTTGCCTCACC | 10277 |
rs199665544 | snp | C/T | 0.00028387 | 0.0119103 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178676 | ATTGTTTGAAGAAGT[C/T]ATTTCAAAGATGCGG | 10277 |
rs199676522 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088389 | TTTAAATTTATTTTA[-/T]TTTTTTTTTGAGATG | 10277 |
rs199707934 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10113780 | TCAAACATAAGATGC[-/T]TTTCGGCCGGACGCA | 10277 |
rs199753032 | snp | A/G | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10134995 | TTTCACAGACAGATG[A/G]TAGATTGGTGTCTAC | 10277 |
rs199767831 | snp | A/G | 0.00136005 | 0.0260418 | intron-variant | UBE4B | GRCh38.p7 | 1:10146920 | CCCTGTAGGGACTTA[A/G]CTACTGACTGATCTT | 10277 |
rs199770696 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054065 | ATTAGAAATATTAGA[-/T]TTTTTTTAAAAAAAA | 10277 |
rs199774926 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103715 | GGCTCACTGCAACTC[C/T]CACCTCCTGGGTTCA | 10277 |
rs199783947 | in-del | -/AAGG | 0.0221141 | 0.102801 | intron-variant | UBE4B | GRCh38.p7 | 1:10070769 | TTAATTATATGTTAA[-/AAGG]AAGAAGTGGCAGATT | 10277 |
rs199801311 | in-del | -/TTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156240 | TTTCATTTTCTTTTC[-/TTT]TTTTTTTTTTTTTTT | 10277 |
rs199802380 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178348 | TAGCTGTAAAAATTC[-/A]AAAAAAAAAGCCCGT | 10277 |
rs199810574 | snp | C/G | 0.00199792 | 0.0315431 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095549 | GCAATCTCAGTCTCT[C/G]TCACGTTCCCAGAGC | 10277 |
rs199837285 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171242 | TGAGAAATACGGCTT[C/T]GAACCAAAGAAGCTG | 10277 |
rs199840708 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037730 | TGGCCAATTTTTGTA[-/T]TTTTTTCTAGAGACA | 10277 |
rs199882034 | snp | A/G | 0.000132477 | 0.00813761 | intron-variant | UBE4B | GRCh38.p7 | 1:10106631 | TTGCGGTGCAGGGAA[A/G]GGAGATTAACACGGT | 10277 |
rs199893860 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072447 | CATCTTTTTTTTTTT[A/G]AAACAGGTTTAGGTA | 10277 |
rs199895289 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105893 | TTTAGTCATTGGAAG[G/T]GGAATTCTCTTTTCT | 10277 |
rs199899474 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166973 | CACACACACACACAA[A/C]AAAAAAAAATTAGCT | 10277 |
rs199905525 | snp | C/T | 0.00199803 | 0.031544 | intron-variant | UBE4B | GRCh38.p7 | 1:10126894 | TAAAACTTTGTTCTT[C/T]TTCTTTAACTCATTC | 10277 |
rs199915203 | snp | A/G/T | 0.000166059 | 0.00911064 | intron-variant | UBE4B | GRCh38.p7 | 1:10179598 | AGGTGCAGCGCTGGC[A/G/T]TCAGTACCAAGAGAT | 10277 |
rs199915638 | snp | G/T | 6.65059e-05 | 0.00576616 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106256 | CTGTTCCCGTGATGG[G/T]CCCGTCTCTTGCCTC | 10277 |
rs199953506 | snp | C/T | 0.35894 | 0.225016 | intron-variant | UBE4B | GRCh38.p7 | 1:10061912 | TTTATCTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs199967568 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107579 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 10277 |
rs199996484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037779 | CAGGCTGGTCTCAAA[C/T]TCCTGGGCTCAAGTG | 10277 |
rs200003707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132365 | TTTTAAAAATAAATT[G/T]CAGCAAGAGCTTTTT | 10277 |
rs200024111 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087022 | AGTGGACAAGACCAG[A/G]GCAGATGTTGTGGTA | 10277 |
rs200025605 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170383 | GTATAAATCCAGTTA[-/T]TACATTTCATGAAAA | 10277 |
rs200027159 | in-del | -/AA | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10144410 | TAGTGCCATCCATTC[-/AA]AGACACATCATTGTT | 10277 |
rs200027493 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085653 | GTAAAGGGTTATAGG[-/T]TTTTTTTTTAACATC | 10277 |
rs200040981 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097055 | AAAAAAAAAAAAAAA[-/T]AATAATAATAATAAT | 10277 |
rs200064729 | in-del | -/ACACACACACACACACAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111045 | CTTTCTCTGTCTCTG[-/ACACACACACACACACAC]ACACACACACACACA | 10277 |
rs200094600 | snp | C/T | 0.000132238 | 0.00813028 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168150 | GGATCAGCAGCAGGC[C/T]CGTCAGTCTCAGCTT | 10277 |
rs200098303 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133209 | TCCTTGACTAGTAAT[-/A]AATAATGAATGAATG | 10277 |
rs200109253 | in-del | -/G | 0.0134914 | 0.0810167 | intron-variant | UBE4B | GRCh38.p7 | 1:10120234 | AGCTTACATTTAAAA[-/G]TTTAGGCCGAGCATG | 10277 |
rs200184210 | snp | C/T | 0 | 0 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171320 | CGCGAAAGCCATTGC[C/T]GACGACCAGGTCAGT | 10277 |
rs200309857 | snp | C/G | 0.000132807 | 0.00814774 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103084 | AGTTTAAGCAGAACC[C/G]AAAAGAAGGTAGGAA | 10277 |
rs200319906 | in-del | -/AGG | 0.0325976 | 0.123435 | intron-variant | UBE4B | GRCh38.p7 | 1:10066812 | TCGGGAGGCTGAGAC[-/AGG]AGAATGGCATGAACC | 10277 |
rs200365375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074205 | CTACCTGTATGTGCG[C/T]CTGGTTCTTGTTATG | 10277 |
rs200365703 | in-del | -/CGCTCTTGG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050134 | GCTGGAGTGCAGTGG[-/CGCTCTTGG]CTCACTGCAACCTCC | 10277 |
rs200375353 | snp | C/T | 8.29882e-05 | 0.00644106 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151340 | GATACTCTCCCCAGG[C/T]GCTTTATGAGCCCTG | 10277 |
rs200414852 | snp | A/G | 0.000198082 | 0.00994996 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135047 | CCTTTGGGTACTGCA[A/G]CAGCTAAGTACAAAA | 10277 |
rs200443424 | snp | A/G | 3.29935e-05 | 0.00406149 | intron-variant | UBE4B | GRCh38.p7 | 1:10129347 | CTACAAATGACAGTC[A/G]GTTTAAGATGAAATG | 10277 |
rs200457569 | in-del | -/AATAATAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167442 | AACTCCGTCTCAAAA[-/AATAATAAT]AATAATAATAATAAT | 10277 |
rs200469707 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097879 | GTCCTTATTTTTTTT[-/T]GGAGACGGAGTCTCA | 10277 |
rs200486578 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125959 | ATGTTGATTGTTGGC[A/C]TGTTTATCTTGTTTT | 10277 |
rs200525963 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10080003 | GGGCATGAACTTGTG[-/A]AAGAGGTGCAGATGC | 10277 |
rs200531019 | in-del | -/AAAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055942 | AAACAAAACAAAACA[-/AAAC]AAACCAGAAGTAGAA | 10277 |
rs200546136 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130552 | GTCCTGGCTGTGGGC[A/G]GGAGCTGCAGAGACT | 10277 |
rs200554034 | snp | C/T | 0.000248503 | 0.011144 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106331 | TCAGTCCTCACAGTG[C/T]AGCCTCTGGAACTGC | 10277 |
rs200598100 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086109 | CCCGAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA | 10277 |
rs200601774 | snp | C/G | 0.000118876 | 0.0077087 | intron-variant | UBE4B | GRCh38.p7 | 1:10132341 | AAATAGTTTTAATTT[C/G]TTTCTTCTTTTTAAA | 10277 |
rs200667729 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035400 | TACTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTG | 10277 |
rs200672184 | in-del | -/A | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181278 | GTGGAAAAAAAAAAA[-/A]GGGCAGGGCGGGTGG | 10277 |
rs200689097 | snp | C/T | 1.83407e-05 | 0.0030282 | intron-variant | UBE4B | GRCh38.p7 | 1:10106157 | TCTCAAGTTTTTCTT[C/T]GATTTTTCTCTTCTT | 10277 |
rs200700529 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166375 | TCTGTGGTGTGACAG[C/T]CTCACAGTTTGGAAA | 10277 |
rs200723341 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089517 | GAAAAAAAAAAAAAA[-/G]GTTTTCAGGGGTGAG | 10277 |
rs200770582 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065930 | GCTTTTTCAATTCAA[-/T]TTTTTAAAAAATGGA | 10277 |
rs200822867 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121248 | GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGCAGG | 10277 |
rs200835267 | snp | A/G | 0.000345927 | 0.013147 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130779 | ACACTCGTGTGGTTA[A/G]CCAATCATTGCAGCA | 10277 |
rs200855506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048174 | TTGGGAGGCAACTAG[A/C]TTTTCTACCACAGGG | 10277 |
rs200871354 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | UBE4B | GRCh38.p7 | 1:10126886 | CCTCATGGTAAAACT[C/T]TGTTCTTTTTCTTTA | 10277 |
rs200901608 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086143 | CGCCAGGCTAATTTT[C/T]TGTATTTTTAGTAGA | 10277 |
rs200940952 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | UBE4B | GRCh38.p7 | 1:10171725 | CTCTACTAAAGATAC[-/A]AAAAAATTACCTCAG | 10277 |
rs200955920 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079146 | CCCTTTGGCAAACTG[A/G]GGAAGCCTTTGATTG | 10277 |
rs200980839 | snp | C/T | 0.000769895 | 0.019605 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106213 | CTCTATGAAAGTAGT[C/T]CGGCTCCCACTCCCA | 10277 |
rs201009990 | in-del | -/AGTAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108836 | CTATTGCATGATTAT[-/AGTAAT]AAAGCAGGCATCCTT | 10277 |
rs201059375 | in-del | -/AAAG | 0.0659589 | 0.169201 | intron-variant | UBE4B | GRCh38.p7 | 1:10080427 | ATCTCAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 10277 |
rs201068175 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168485 | GTCACCACATAGTCT[G/T]CAGCCACTTCCAAAT | 10277 |
rs201076230 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033457 | GGGAACAAGCGGCTG[A/C]AGTAGTCTGTGGGGC | 10277 |
rs201077081 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088389 | TTTTAAATTTATTTT[-/A]TTTTTTTTTGAGATG | 10277 |
rs201127396 | snp | A/C/G | 9.89322e-05 | 0.00703259 | intron-variant | UBE4B | GRCh38.p7 | 1:10130457 | CATTTTTACCCCACC[A/C/G]GCCTGTTCAGCGGCT | 10277 |
rs201131968 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121375 | ACAACAAACAACAAC[-/A]AAAAAAAACATATAA | 10277 |
rs201165696 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101162 | GGAGGTTGATGAAAA[C/T]GATCGAAGAGAAAAG | 10277 |
rs201167205 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111026 | TCTCTCTGTCTCTCT[A/C]TGTCTTTCTCTGTCT | 10277 |
rs201194300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143327 | GAATCGCTTCAACCC[A/G]GGAGTCAGAGGTTGC | 10277 |
rs201205717 | snp | C/T | 6.73707e-05 | 0.00580352 | intron-variant | UBE4B | GRCh38.p7 | 1:10168094 | TTGCTGAGCTGATGA[C/T]CAGGACCGAGCCTTA | 10277 |
rs201222800 | snp | A/C | 6.6443e-05 | 0.00576343 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151337 | TCAGATACTCTCCCC[A/C]GGCGCTTTATGAGCC | 10277 |
rs201265548 | snp | C/T | 0.000378828 | 0.0137576 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105679 | CTTGCTAAACACTGG[C/T]TCCAATCCAGGAACA | 10277 |
rs201302266 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145611 | TCTCAAAAAAAAAAA[C/T]ACAACAACAACAAAA | 10277 |
rs201315689 | in-del | -/G | 0.0174175 | 0.0916809 | intron-variant | UBE4B | GRCh38.p7 | 1:10166427 | AGTCCACAGGCACTT[-/G]GTAGAGGCAGAGAGG | 10277 |
rs201328501 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068189 | GCCTACCACCACACC[C/T]GGCTAATTTTTGTAT | 10277 |
rs201352258 | in-del | -/AAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152260 | CAAGACTCCGTCTCA[-/AAT]AATAATAATAATAAT | 10277 |
rs201367251 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10092219 | ACATAGTGAGACCCA[-/TC]TCTTTTGTTTTGTTT | 10277 |
rs201394763 | in-del | -/TTTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103400 | GAGCATTACCTCCTC[-/TTTA]TTTATTTATTTATTT | 10277 |
rs201415119 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10070607 | GAATCATCCACTCTG[-/T]TTTTTTTTACATCTG | 10277 |
rs201460610 | snp | A/G | 6.59e-05 | 0.00573983 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072146 | CGGCATCAGCCCCAG[A/G]ACCCTCTCAGAGTCT | 10277 |
rs201495094 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041524 | ATTTTTAGTAGAGAT[A/G]GGGTTTCTCCAAGTT | 10277 |
rs201532358 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061266 | AAAACAAGTTTGTTT[-/G]TTTTTTTGTGAGACA | 10277 |
rs201571950 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084865 | ACCATTCCTGGCTAA[-/T]TTTTTTTTTTGTATT | 10277 |
rs201579904 | snp | A/G | 3.314e-05 | 0.00407049 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106327 | CCCCTCAGTCCTCAC[A/G]GTGCAGCCTCTGGAA | 10277 |
rs201593320 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10089194 | GTATTTTTAGTAGAG[A/C]CAGGGTTTCACCATA | 10277 |
rs201595565 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155355 | TAATCCCCACGGCAG[C/T]CCTAAAGATAGTACT | 10277 |
rs201641352 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037731 | GGCCAATTTTTGTAT[A/T]TTTTTCTAGAGACAG | 10277 |
rs201699830 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178730 | AGCAATAGAAAAATT[C/T]AAGCTGCTCGCCGAG | 10277 |
rs201702683 | in-del | -/CC | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10128509 | TTAAAGGTGTTTCTG[-/CC]TGGCTCCCCACCCCA | 10277 |
rs201712464 | snp | A/C | 1.65053e-05 | 0.0028727 | intron-variant | UBE4B | GRCh38.p7 | 1:10129498 | GTGAATATATCATAA[A/C]CCAGAAGGCATTCCT | 10277 |
rs201715112 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | UBE4B | GRCh38.p7 | 1:10118340 | TTTTTTGTTTTTTTT[-/T]GTTTTTTGAGATGGA | 10277 |
rs201734678 | snp | C/T | 0.000197798 | 0.00994283 | intron-variant | UBE4B | GRCh38.p7 | 1:10147123 | TGTTTCCCTTGTCCC[C/T]CCTTGGCTGGGCTCT | 10277 |
rs201736832 | snp | C/T | 0.000365345 | 0.0135107 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106409 | CTCACCCATGGGCGT[C/T]CTCAGGCGTCTCCAT | 10277 |
rs201751777 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075168 | TCTGCTTCTGTAGCA[A/C]AAAAGCAGCCATAGA | 10277 |
rs201813896 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10138400 | ATGCACCTGGCCCAA[-/T]TTTTTGTATTTTTTG | 10277 |
rs201833160 | snp | A/G | 4.97624e-05 | 0.00498786 | intron-variant | UBE4B | GRCh38.p7 | 1:10130853 | GAGGAAGTATCAAAG[A/G]TGAGCTCCAGATACA | 10277 |
rs201844344 | snp | A/G | 0.00199792 | 0.0315431 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171205 | GTGGCCCCAAGTGCC[A/G]TGACCTGAAAGTTGA | 10277 |
rs201875729 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072099 | CCCACTCACCTCTCC[C/T]CAGAGGGAGAACCCT | 10277 |
rs201918108 | snp | C/G | 0.000336355 | 0.012964 | intron-variant | UBE4B | GRCh38.p7 | 1:10103121 | TCAGCAGTCTTACTG[C/G]AGAGTACTCGACAAG | 10277 |
rs201933475 | in-del | -/TTA | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095297 | AATGTTCCTATGATT[-/TTA]TTATTGTTTCCAGCT | 10277 |
rs202002246 | in-del | -/TAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159707 | AAATAAATAAATAAA[-/TAAA]AATTTTATCCCACCT | 10277 |
rs202006831 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111004 | CTGTCCCTCTCTTCT[C/T]TCTGTCTCTCTCTGT | 10277 |
rs202036384 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10092224 | GTGAGACCCATCTCT[C/G/T]TTGTTTTGTTTTGTT | 10277 |
rs202048066 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179975 | GTTCCGCCGCCCACC[C/G]TCTGCTAGACACAGC | 10277 |
rs202058348 | snp | G/T | 0.000708723 | 0.0188111 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126826 | ACAAGGCCTGGCTCT[G/T]GCTGCCAAAGAGTGC | 10277 |
rs202058978 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135735 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 10277 |
rs202071008 | in-del | -/AG | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10159667 | TCCAGCCTGGGCGAC[-/AG]AGTGAGACTCCGTCT | 10277 |
rs202084653 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090114 | AGGAATCAGGCAGCC[-/TG]TGTGTGTGTGTGTTT | 10277 |
rs202097679 | snp | C/G | 1.65556e-05 | 0.00287707 | intron-variant | UBE4B | GRCh38.p7 | 1:10105471 | GGCTGTGTAACCTGT[C/G]TTCGAACTGTGTGTA | 10277 |
rs202107114 | in-del | -/AAAG | 0.0111196 | 0.0737302 | intron-variant | UBE4B | GRCh38.p7 | 1:10175677 | AAATAAATAAATAAA[-/AAAG]AAAGAAAATAAAAAA | 10277 |
rs202193012 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179116 | GAAGTCCTAAGACAA[-/G]AGAATTCCAGCCTGC | 10277 |
rs202232853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10118503 | CCACCACACCCAGCT[A/C]ATTTTTTTTTTTTCT | 10277 |
rs202235278 | snp | A/C | 0.000632206 | 0.017768 | intron-variant | UBE4B | GRCh38.p7 | 1:10161115 | CAGGGAGATGTATGA[A/C]CATGTACAATATAAT | 10277 |
rs367543505 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127600 | AAAATATCAAAATGA[A/G]ATTAGTTTATTCTAT | 10277 |
rs367557718 | in-del | -/AAAA/AAAAA | 0.137187 | 0.223099 | intron-variant | UBE4B | GRCh38.p7 | 1:10134049 | GTAAAACCCTGTCTC[-/AAAA/AAAAA]AAAAAAAAAAAAGAA | 10277 |
rs367558769 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10088670 | GCCACCACGCCTGAC[C/T]GTATTTTATTATTTT | 10277 |
rs367563506 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058227 | AAATGTGGTTAATCA[A/G]TCAAGCTTTTTGTAA | 10277 |
rs367565056 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138472 | TTCCTGACCTCAGGC[A/G]ATCCGACTGCCTCCG | 10277 |
rs367577871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10076118 | AGCTGGCATGAGGAA[A/G]GTGATGGCTTGTGTT | 10277 |
rs367582496 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105674 | AATCTCTTGCTAAAC[A/G]CTGGCTCCAATCCAG | 10277 |
rs367622405 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113818 | ACGCCTGTAATCCTA[A/G]CCCTTTGGGAGGCCG | 10277 |
rs367645923 | snp | A/T | 0.000234039 | 0.010815 | intron-variant | UBE4B | GRCh38.p7 | 1:10161334 | TGCAGGCCATCTGCC[A/T]CCACACACGGGCAGA | 10277 |
rs367710638 | in-del | -/CAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123389 | GAGCCGAGATTACAC[-/CAC]TGCATTCCAGCCTGG | 10277 |
rs367764811 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101977 | TGCTCTGCATTTAGG[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs367793705 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173143 | TACAAAGTAGTGGCT[C/T]GTAAGAGGGTTAGGA | 10277 |
rs367826428 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111528 | TGCACGCACACCGTC[A/G]TTCTTCATCCGCCTG | 10277 |
rs367839913 | snp | A/G | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181397 | ATTCATGTCAGTCTC[A/G]ACATTTGGTTCTCAT | 10277 |
rs367841509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054447 | CACACCTCTTATGCC[A/G]TGAATTCATAGGTAA | 10277 |
rs367847688 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115749 | CAACCTAGATCATAC[A/G]GCCTACTACACACCT | 10277 |
rs367871589 | snp | C/T | 0.000231704 | 0.010761 | intron-variant | UBE4B | GRCh38.p7 | 1:10161296 | CCCCGGGTGAGGACG[C/T]GGTCCAGAGGCTTGG | 10277 |
rs367922485 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076247 | CTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs367933352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115298 | AGCAAATATCATAGT[C/T]GCTCTCTTGCCCAGG | 10277 |
rs367982032 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057102 | CAGGTGTGAGCCACC[A/G]CACCTGGCCCCTTAT | 10277 |
rs367994851 | snp | A/T | 1.65127e-05 | 0.00287334 | stop-gained, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126810 | TATTTATCCCCATTT[A/T]ACAAGGCCTGGCTCT | 10277 |
rs368008568 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062888 | TTGTACCTGGGAGGC[A/G]GAGGTTGCAGTGATC | 10277 |
rs368019306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164740 | CTGGCTGTTCCTGCT[C/T]ATCTCCCTGACGTCT | 10277 |
rs368062433 | snp | A/T | 1.67153e-05 | 0.00289091 | intron-variant | UBE4B | GRCh38.p7 | 1:10149163 | TCATTTAATAAATTG[A/T]CCTTTTTTTCTCTTT | 10277 |
rs368072349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10138037 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCTTCA | 10277 |
rs368078354 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164705 | TTTGGCTTTGAAGTC[A/T]CTTTCTACCTCCCAC | 10277 |
rs368080378 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104816 | ACAAGTGTCTTACAC[A/G]TGTTAAGTGGCAACT | 10277 |
rs368127453 | snp | C/T | 5.34736e-05 | 0.00517049 | intron-variant | UBE4B | GRCh38.p7 | 1:10178863 | TTCTTTTGAGTTAAC[C/T]GGAAATCGATAACAT | 10277 |
rs368131040 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175174 | ATGCCAGAGAAGTGG[A/G]ATACCACATTGGTCC | 10277 |
rs368177988 | in-del | -/ATTTCTTTATA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072707 | AAAAAGTAAAAGTTT[-/ATTTCTTTATA]ATAAATGAGCTGATG | 10277 |
rs368180787 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141043 | TGATTTTAGCCCTAC[A/G]TAGAAGTATATCAGC | 10277 |
rs368201101 | in-del | -/ATAGTCTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168478 | GTCTGATGTCACCAC[-/ATAGTCTA]CAGCCACTTCCAAAT | 10277 |
rs368205151 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134547 | AAAAGAATGTATAAA[A/T]TGCCTCTTATATAAA | 10277 |
rs368215683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095395 | GTGCGTGTTTACTGT[C/T]GCTATTACAAATAAC | 10277 |
rs368234012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10034531 | TACAAGGAATTTCCT[A/G]TGATTCTACTGCCTT | 10277 |
rs368254644 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149303 | TGCCTTTAATATTTT[A/T]CATAGTTCTAATATG | 10277 |
rs368261118 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082293 | CGCTTGAACCCAGGG[A/G]TTTAAGACTAGCCTG | 10277 |
rs368271273 | in-del | -/AC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111214 | TACACTCCACATACT[-/AC]ACACACACACACCAC | 10277 |
rs368273980 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10035919 | GGCTAATTTTTTGTG[-/T]TTTTTAGTAGAGACG | 10277 |
rs368280932 | snp | A/G/T | 3.29875e-05 | 0.00406112 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102961 | AGGAGCCTTCCTCGG[A/G/T]CCCTGAAGTGTCTGA | 10277 |
rs368294631 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132377 | ATTTCAGCAAGAGCT[C/T]TTTAAGATTCTGCAT | 10277 |
rs368296617 | snp | C/T | 4.94466e-05 | 0.00497201 | intron-variant | UBE4B | GRCh38.p7 | 1:10129460 | TTTGGTAAGCACTCA[C/T]CTGATGGGCTTGCAC | 10277 |
rs368354280 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152626 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs368376272 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159009 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs368390464 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10128783 | TTGAAAATAATGTTT[C/G]ATTGAGTTACCATGG | 10277 |
rs368391513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10104541 | ACCTTTCTCTTTTCT[A/G]TGCTGCCTATCTTCT | 10277 |
rs368400893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10059379 | GGACACTATTGTCAG[A/G]GCTCTGCCCTTTTGG | 10277 |
rs368445541 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061077 | TCTGTTTTTTTTTTT[-/T]ATCTCAAAAGACAAC | 10277 |
rs368465936 | snp | C/T | 3.31472e-05 | 0.00407093 | stop-gained, intron-variant | UBE4B | GRCh38.p7 | 1:10106357 | ACTGCTGCGGGAAGC[C/T]AGCCTTCATCCCCGC | 10277 |
rs368472108 | snp | G/T | 8.26631e-05 | 0.00642843 | intron-variant | UBE4B | GRCh38.p7 | 1:10137016 | TTCAGCTTTTTCTCT[G/T]ATTGAGACATGTAAT | 10277 |
rs368483223 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072595 | GAACACCTCTAATTG[C/T]AGATTTCCTCGTCTT | 10277 |
rs368487440 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095077 | AGCCACTGCATCGGC[C/T]TGGTTTATTAATATA | 10277 |
rs368509846 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137638 | ATTCTCTTTTTGGCT[C/T]GTTCTGTGGCATGAG | 10277 |
rs368522291 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053380 | AGTCTCGATCTCCTG[A/T]CCTCGTGATCCACCC | 10277 |
rs368533002 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037130 | CCTCCCGGGTTCAAG[C/T]GATTTTCCTGCGTCA | 10277 |
rs368574334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10134373 | AAAAATTTGCCGGGC[A/G]TGGTGGCGGGTGCCT | 10277 |
rs368575519 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159270 | TACCTGAAATCTGAG[C/T]GACTGCTTAAACCTG | 10277 |
rs368633240 | in-del | -/TTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104677 | TGCTACTTGTTATTC[-/TTA]TTATAAATCTTAAGA | 10277 |
rs368654870 | snp | A/G | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103086 | TTTAAGCAGAACCCA[A/G]AAGAAGGTAGGAATC | 10277 |
rs368660126 | snp | A/G | 3.33667e-05 | 0.00408439 | intron-variant | UBE4B | GRCh38.p7 | 1:10168116 | CGAGCCTTACTCAGC[A/G]TCTGTTCGATGTGTC | 10277 |
rs368666283 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114729 | ATTAGCTGTACATGG[C/T]GGCGAGCGCCTGTAG | 10277 |
rs368673422 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094095 | ATTCTTCTTTTTTCA[A/T]AGGAAGATATTCATA | 10277 |
rs368686403 | snp | C/T | 0.000965201 | 0.021947 | intron-variant | UBE4B | GRCh38.p7 | 1:10105770 | TTCTCTTTGCACATC[C/T]TACTGGTAGTAAAAT | 10277 |
rs368703770 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111042 | TGTCTTTCTCTGTCT[C/G]TGACACACACACACA | 10277 |
rs368711823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10142247 | ATTTTTTTCATGAAG[A/G]CCTGTTACCTATAAA | 10277 |
rs368736936 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10173839 | GGGTGGGCACAGCAC[A/G]CCCAGTGAGGTGATG | 10277 |
rs368755037 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033020 | GGGGCGAGGGGGAAA[A/G]AGTAGGGGTGGAGGG | 10277 |
rs368823983 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10092273 | TCTGTCACCCAGGCC[A/G]GAGTGCCGTGGCACG | 10277 |
rs368824292 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061730 | CTCTACCCAGAAATC[A/G]AGCCGCACCAGCAAA | 10277 |
rs368856322 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044373 | TTCCATATTTAATTG[C/G]CAAACACCACCAAGT | 10277 |
rs368878951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144513 | GGCTGGGGCAGGCAG[A/G]CCACAAGGTCAGGAG | 10277 |
rs368886550 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159364 | TGAACTCTTGAATTA[C/T]TCTTCAAAAATTTTA | 10277 |
rs368921206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10131378 | GCTACCTAGCTACTC[A/G]GGAGGCTGAGGCACA | 10277 |
rs368961834 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154576 | GGCTCAGTGACTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs368975947 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151395 | TGTTGTGATGTTGTG[C/T]AACCAGAACTACATC | 10277 |
rs369019073 | snp | A/C/G | 0.000176089 | 0.00938165 | intron-variant | UBE4B | GRCh38.p7 | 1:10132519 | TTTCGCTGTTTGTCA[A/C/G]ATTCATTCATCTGAC | 10277 |
rs369030513 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097376 | GACAACAGGGGTCCA[A/G]GATATATCTAAACAT | 10277 |
rs369087504 | in-del | -/GC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101497 | TTCTGTTGGTCTTTT[-/GC]TTTTTTTTTTTTTTT | 10277 |
rs369093933 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148183 | GGTGAGCGGAGATCA[C/T]GTCTCTGCACTCCAG | 10277 |
rs369101920 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153522 | AAAAAAAAAAAAGGG[A/T]AAAAAGACTGGGTTT | 10277 |
rs369103530 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072187 | GTCCACAACATGACC[C/T]CAGCTACCTCCCCAA | 10277 |
rs369149021 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175754 | CTAAGTAATTGCTCC[C/T]TCCTCTAACCTACCA | 10277 |
rs369172773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048754 | TCATTGCTGACTGGA[G/T]CAAGTTCAAGAGAGA | 10277 |
rs369214323 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076247 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs369223611 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060878 | CCTCCTGAGTAGTTA[C/T]GACTACAGGCACGTG | 10277 |
rs369253346 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10151593 | CAGTGTAGCACATGG[C/T]AGGCCAACTTAGGTA | 10277 |
rs369273139 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063595 | TCCACACAGTAGCTA[C/G]AGTGATTTGTTTTAA | 10277 |
rs369275382 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142055 | TGTCATTTTTTTTTT[-/T]CTATAAGCTCCACCA | 10277 |
rs369276142 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078264 | TCCACCTGTCTCAGC[C/T]TCCCAAAGTGCTGGG | 10277 |
rs369280542 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164113 | TGGGAGGCCGAGGCC[A/G]GCAGATCACCTGAGG | 10277 |
rs369303157 | snp | C/G | 1.65427e-05 | 0.00287595 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103065 | CTTTCTTCTCTTTCT[C/G]CACAGTTTAAGCAGA | 10277 |
rs369445174 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116643 | TTAACTTTGTTTAAT[A/G]TCCTCAAATTTAACC | 10277 |
rs369451454 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085590 | ATTGTAAACTATGCA[A/G]CATGGTTTTCAAAAA | 10277 |
rs369455724 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054220 | TGTAAGTAATATCTG[G/T]CTGTTTTCTAACCAA | 10277 |
rs369471209 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036502 | TTAATTTAAAAAATC[-/T]TTTTTTTTTTTTGTA | 10277 |
rs369488590 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090769 | CTGTGCTCTTTTTAC[A/G]GTGGAATTTAGAAGC | 10277 |
rs369539347 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181165 | TTTCTTTTCCTTTTT[C/T]CCCTCCACAGACAAT | 10277 |
rs369540684 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174347 | GCAGTGAGCTGAGAT[C/T]GCACCGCTGCATTCC | 10277 |
rs369571626 | in-del | -/AAAT | 0.19334 | 0.243495 | intron-variant | UBE4B | GRCh38.p7 | 1:10159684 | GTGAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 10277 |
rs369572517 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100013 | TTATTTTTTTGAGAT[A/G]GAGTCTCGCTCTGTC | 10277 |
rs369581649 | snp | C/G | 1.68624e-05 | 0.0029036 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106500 | CAGTTCCAGACAGAG[C/G]CCCAGCAGCACGGGT | 10277 |
rs369587261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162823 | GTGTCTGTTATTCCC[A/G]TCTCCGTCCATGTGT | 10277 |
rs369621515 | in-del | -/TAAAAA | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10139232 | AAAACCCGTCTCTAC[-/TAAAAA]TACAAAAATTAGCTG | 10277 |
rs369632370 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131823 | CTGGGCATGGTGGCG[G/T]GTGCCTGTAATCCCA | 10277 |
rs369635814 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155464 | AGTGGCAGCAACCTC[A/G]CAGATGCCCTTTAGC | 10277 |
rs369645708 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093952 | TGCCTTCCTCGGCCC[C/T]TCAAAGTGCTGAGAT | 10277 |
rs369659612 | snp | C/T | 1.67049e-05 | 0.00289002 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151557 | CCTGATGAAGTTTTA[C/T]ACAGGTAGGTTGCTG | 10277 |
rs369668231 | snp | A/G | 0.000107974 | 0.00734679 | intron-variant | UBE4B | GRCh38.p7 | 1:10168287 | TGAGTAGAAACCCGG[A/G]GCTCTGTTTGGTGGT | 10277 |
rs369680704 | snp | A/G | 1.64866e-05 | 0.00287106 | intron-variant | UBE4B | GRCh38.p7 | 1:10137236 | CCGTGTCCTGGGATT[A/G]CCTGAGTTACCACTT | 10277 |
rs369690787 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077838 | ACATAACTAGTGCCT[A/G]TGGAACCAAGTCCAC | 10277 |
rs369716611 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159683 | GAGTGAGACTCCGTC[A/T]CAAATAAATAAATAA | 10277 |
rs369737128 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048436 | TAAAATCATGAGAAT[A/G]GACAGATTTTACCTA | 10277 |
rs369746054 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10136285 | CAAGACCAGCCTGGG[C/G]AAAATAAGGAAACCC | 10277 |
rs369752834 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069330 | ATATTTAGAGAGTAC[C/T]TACCATGTGTCAGAC | 10277 |
rs369759223 | snp | A/G | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181673 | AAATTAGCCGGGCGT[A/G]GTGGCAGCGCCTGTA | 10277 |
rs369759551 | snp | A/C | 1.83602e-05 | 0.00302982 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106573 | CCCTCCTCCCTGAGG[A/C]TCTCTCCTAGGTATT | 10277 |
rs369847239 | in-del | -/AAACC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055946 | AAAACAAAACAAAAC[-/AAACC]CAGAAGTAGAAGTAG | 10277 |
rs369854673 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069092 | TTTCTTTCTTCAACC[A/G]CATATTATAGTGAGT | 10277 |
rs369907046 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162319 | GTTGGGACTACAGGC[A/C]CCTGCCACTACGCCT | 10277 |
rs369911066 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10097822 | CTCAAAAAAAGTAAT[A/G]AATAAATAAACACAT | 10277 |
rs369929304 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137202 | CTATCCGGGAGCTCA[A/G]TAGGTATGTGCCATG | 10277 |
rs369937523 | snp | C/G/T | 6.72578e-05 | 0.00579871 | intron-variant | UBE4B | GRCh38.p7 | 1:10121936 | AGTTGACTTCATCAC[C/G/T]GTCCCTAATGTTCAT | 10277 |
rs369973074 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088077 | CATGCCTCTTCTTTT[A/G]TATTTTTGAGCACTG | 10277 |
rs369982218 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097218 | CCACAAAGAACAAAG[C/T]AGATGAAAAATATAA | 10277 |
rs370043403 | snp | G/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126798 | TTTTCTTATAGATAT[G/T]TATCCCCATTTTACA | 10277 |
rs370054373 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083737 | AGAGGTTGAAATCCT[G/T]TGCTTTTTGCTTATT | 10277 |
rs370055558 | snp | A/C | 9.9453e-05 | 0.007051 | intron-variant | UBE4B | GRCh38.p7 | 1:10145080 | ATAGACCAGCCTCAT[A/C]GTGATAATTTTCCCA | 10277 |
rs370056407 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059103 | GGTGTGGCGGTGGGC[A/G]CCTGTAGTCCCAGCT | 10277 |
rs370063602 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115161 | AAATACTTTAATACC[A/G]TACTTTTTTTTTTTT | 10277 |
rs370131299 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036614 | TGGGAGCCAGACAAA[C/T]AGTTATTTTGGGAAA | 10277 |
rs370165181 | in-del | -/TCT | 0.00087813 | 0.0209355 | intron-variant | UBE4B | GRCh38.p7 | 1:10102932 | AAATTAACCTGCAAA[-/TCT]TCTTCTTCACCAGGA | 10277 |
rs370168292 | snp | A/G | 1.65707e-05 | 0.00287838 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106296 | TGCAGCCAGCCAGTT[A/G]GCTGTGCCTTCCACT | 10277 |
rs370174226 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106650 | GATTAACACGGTTTG[A/G]AAGAAGTGCTGTGTG | 10277 |
rs370234978 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069558 | TTATTTTTTTGAGAC[A/G]GAGTCTCACTTCATC | 10277 |
rs370242612 | snp | C/T | 3.37564e-05 | 0.00410817 | intron-variant | UBE4B | GRCh38.p7 | 1:10179370 | GTTTTCTTTTTCAGT[C/T]GTGGGCTCTCAGTAG | 10277 |
rs370248917 | snp | C/T | 0.000529021 | 0.0162552 | intron-variant | UBE4B | GRCh38.p7 | 1:10135201 | TGTGAGTACTGTGTT[C/T]GTGACTCGGTCATTA | 10277 |
rs370286154 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094636 | AGACGGGGTTTCACC[A/T]TGTTAGCCAGGATGG | 10277 |
rs370286248 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133480 | CATTGTTGTATTATT[A/T]TTTTTTTCTTAACAG | 10277 |
rs370298894 | snp | A/G | 0.000248866 | 0.0111522 | intron-variant | UBE4B | GRCh38.p7 | 1:10158513 | CTCGTGTCACAACTT[A/G]CTTTCTTGCAAATCG | 10277 |
rs370316464 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177317 | TTGAGGTCAGGAGAT[C/T]GAGACCAGCCTGGCC | 10277 |
rs370333584 | snp | C/T | 6.80677e-05 | 0.00583346 | intron-variant | UBE4B | GRCh38.p7 | 1:10132495 | CAGGTAGGATTCCTA[C/T]AGACTGCTTTTCGCT | 10277 |
rs370388717 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037982 | TTCCGGGTGTGGTCA[A/G]GATTTTAGAAAGTGT | 10277 |
rs370398350 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142274 | TAAACTCTTGTGATA[C/G]CCGTAGCCATATAGG | 10277 |
rs370413248 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136502 | AAAAAAAAAAAAAAA[G/T]ATTGTGATGGACATC | 10277 |
rs370417352 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10070211 | CCTGGGAGGGGGAGG[A/T]TGCAGTGAGCCGAGA | 10277 |
rs370437852 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036465 | TCTCAGCAGAACCTA[A/G]AACAAATAATATTCG | 10277 |
rs370459881 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051713 | GCAGAAAGGGGACTC[A/C/G]AGGAGTCCCAGGAGA | 10277 |
rs370473673 | snp | A/C | 0.000247952 | 0.0111317 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179991 | TCTGCTAGACACAGC[A/C]AAGGCCAACGAGGCA | 10277 |
rs370482277 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114810 | CGGAGTTTGCACTGA[A/G]CAGAGATCACACCAC | 10277 |
rs370515051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10057791 | AGTAATTGCTAGAAG[C/T]TGGCCTTTGTAAGTA | 10277 |
rs370526193 | snp | A/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105569 | ATGGAAGTGCTAATG[A/T]TGTCCACTCAGACCA | 10277 |
rs370578413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096657 | AACCCAGGAGGTGGA[A/G]GTTGCAGTGAACCAA | 10277 |
rs370597248 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107576 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT | 10277 |
rs370612402 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114801 | CCCAGAAGGCGGAGT[G/T]TGCACTGAGCAGAGA | 10277 |
rs370623276 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109960 | CACCTCGGCCTCCCA[A/C/G]ATTGCTGGGATTACA | 10277 |
rs370639198 | snp | C/G/T | 8.40038e-05 | 0.00648041 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106227 | TCCGGCTCCCACTCC[C/G/T]AGTTTCTGGAGCTCT | 10277 |
rs370717432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056516 | ATCCCTGCTCTCTTG[G/T]AGCTTGTATTGTACT | 10277 |
rs370726035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163993 | CAGCCTCCCAAAGTG[C/T]GGGGGTTACAGACAT | 10277 |
rs370738129 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10103298 | TTATTTTTCATTTCC[A/G]TGATTTCTATAATAC | 10277 |
rs370744387 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125104 | GCACTCCAGCCTGTG[C/T]GACAGAGTGAAATTG | 10277 |
rs370744436 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10087325 | TTGGACTAACTTTCA[A/G]TGTACAGAAAAGTTA | 10277 |
rs370778868 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157218 | TAGAGGCGGGGTTTT[A/G]CTATGTTGGCCAGGC | 10277 |
rs370814557 | snp | A/C | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031922 | AGATGGAGTCGCGCT[A/C]TGTCGCCCAGGCTGG | 10277 |
rs370829494 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041335 | AACCTTTTTGGCATT[-/C]TTTTTTTTTTTTTTT | 10277 |
rs370841758 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050574 | CTTGGTGTAGCTCCT[A/G]CTGGGATATGAACTC | 10277 |
rs370862898 | in-del | -/A | 0.98341 | 0.0431462 | intron-variant | UBE4B | GRCh38.p7 | 1:10117634 | ACTTAAAAAAAAAAA[-/A]GCCTAGTTATTTGTT | 10277 |
rs370876093 | snp | C/T | 6.62241e-05 | 0.00575392 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135088 | AAACAGTTGATCCCA[C/T]GTATATTTTTCACCC | 10277 |
rs370876464 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160684 | AGGTGTGGTGGCTCA[C/T]CTCTGTAATCCCAAC | 10277 |
rs370876734 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129947 | GTGAGCCACCGCACC[A/G]GGCCTGTTTTTTTTC | 10277 |
rs370991793 | snp | C/T | 3.29598e-05 | 0.00405941 | intron-variant | UBE4B | GRCh38.p7 | 1:10147113 | TGCTTCTTCCTGTTT[C/T]CCTTGTCCCTCCTTG | 10277 |
rs371001783 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142858 | TGCCTGGTGTATCGC[A/G]GCACTTTGGGAGGCT | 10277 |
rs371025810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10040434 | TTTTGTATATTTTGT[A/G]GAGACAGGGTCTTGC | 10277 |
rs371035732 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033126 | GGAGGCGGGGCGTGG[C/T]CGGCCTGCTTTGGGA | 10277 |
rs371056737 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101113 | GTACTTTAAGCATGT[C/T]CCAGGTGGATGTGGA | 10277 |
rs371058351 | snp | C/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161284 | TGGGACCAGTTGCCC[C/T]GGGTGAGGACGTGGT | 10277 |
rs371064908 | snp | A/G | 0.000198144 | 0.00995152 | intron-variant | UBE4B | GRCh38.p7 | 1:10126902 | TGTTCTTTTTCTTTA[A/G]CTCATTCAATAGATG | 10277 |
rs371067994 | snp | A/G/T | 0.000377373 | 0.0137316 | intron-variant | UBE4B | GRCh38.p7 | 1:10178834 | GCAAGTGGACTCGTC[A/G/T]TTTTCATGCTGATTT | 10277 |
rs371096292 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110959 | CGTGATCATGCCACT[G/T]CACTCCAGCCTGGGT | 10277 |
rs371098904 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137848 | TGGTCTAGAACCTGC[A/G]TAGTCTGTCTATGAG | 10277 |
rs371106344 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090086 | TGGGGTAAAGGAATT[A/G]CAGCATTATGTTAGG | 10277 |
rs371110163 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071213 | CCTGGCCAATTGGCT[A/G]TTTATTTTTAAATCT | 10277 |
rs371129617 | snp | C/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171307 | ACTGTGCTCGGTTCG[C/T]GAAAGCCATTGCTGA | 10277 |
rs371232127 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065806 | ATTTACTGTGTCATT[G/T]CCATTTGCATTTATG | 10277 |
rs371238521 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123299 | AACTGGGTGTGGTGA[C/T]GGGTGTCTGTAATCC | 10277 |
rs371244798 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066430 | CACCACATCTGACCA[A/T]GAATTTTTTTTTTAA | 10277 |
rs371255144 | in-del | -/CTCTCTGTCT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111022 | TGTCTCTCTCTGTCT[-/CTCTCTGTCT]TTCTCTGTCTCTGAC | 10277 |
rs371256585 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036285 | CCATATGAGGAACAC[A/G]TGTAACCTTTGTGGA | 10277 |
rs371276917 | snp | C/G/T | 3.54844e-05 | 0.00421203 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106544 | CCGCCTCACCCAGTG[C/G/T]CACGAGCAGACGCCC | 10277 |
rs371280849 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097399 | CTAAACATCAAAAAG[A/G]GAGAATAGAGAGTTG | 10277 |
rs371289434 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137422 | CTGAGAGTTCTGAAC[C/G]CTGGATATTTCACTC | 10277 |
rs371330986 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116039 | GCATATCTATCTGTC[C/T]GTAAAACATGTCAAT | 10277 |
rs371332751 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081750 | CTGGCCACCACGCCC[A/G/T]ATTAATTTTTGTATT | 10277 |
rs371339754 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145456 | CAAAAAAAAATTAGC[C/T]GGGCGTGATGGCGGG | 10277 |
rs371347067 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111684 | ATGCAAGGCCAGGCG[C/T]GGTGGCTCACACCTG | 10277 |
rs371356286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044673 | CTGTAACTCCACCGC[C/T]TGGGCTCAAGCGATC | 10277 |
rs371357491 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173250 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGGT | 10277 |
rs371364445 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053577 | ATAGGTAAGCGTGTA[A/C]CGTGGTGGTTTGCTG | 10277 |
rs371378320 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174743 | TTTGCTTCCTTTCAC[A/G]GTGTGGTGTGTGTGC | 10277 |
rs371383122 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052925 | TTCTTGGTTCATAGA[C/T]ACCTGTTTTCTCACT | 10277 |
rs371399268 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10172430 | CACAGAGAGGTTAAA[C/T]AGCTTGCTCGAGGTC | 10277 |
rs371405980 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111915 | TGAGCCAAGATCACA[C/G]CACTGCACTCCAGCC | 10277 |
rs371462606 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | UBE4B | GRCh38.p7 | 1:10149298 | GTAAGTGCCTTTAAT[A/G]TTTTACATAGTTCTA | 10277 |
rs371465177 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138274 | AGCTAATTTTTTGTA[C/T]TTTTAGTAGAGACGG | 10277 |
rs371514724 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10075245 | TTACAAAAACAGGCA[A/G]TAGCCCAGATTTGGC | 10277 |
rs371519935 | snp | A/G | 1.71655e-05 | 0.00292958 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033631 | GTCTCGAGAACAGAA[A/G]GATCTCTCCTTAACG | 10277 |
rs371520523 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040430 | TAATTTTTGTATATT[A/T]TGTAGAGACAGGGTC | 10277 |
rs371535033 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162607 | TCACCGCGCCCAGAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs371537227 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165453 | ATGTCCATATCAGGG[A/T]TGGTGTTAAACATCT | 10277 |
rs371541880 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104845 | CTCTGTCTTACACAT[G/T]TAAGTGGCAATTTTA | 10277 |
rs371559899 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10154343 | GAATAGCTTGAACCC[A/G]GGAGGTGGAGGTTGT | 10277 |
rs371640310 | snp | G/T | 8.52217e-05 | 0.00652714 | intron-variant | UBE4B | GRCh38.p7 | 1:10126776 | CTTATATTTCTGATT[G/T]TGTTTTTTTTCTTAT | 10277 |
rs371641855 | in-del | -/AAT/AATAATAAT | 0.039522 | 0.134904 | intron-variant | UBE4B | GRCh38.p7 | 1:10167441 | AACTCCGTCTCAAAA[-/AAT/AATAATAAT]AATAATAATAATAAT | 10277 |
rs371688777 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106066 | ATTATAATTATTTAG[A/G]TGTTTATCTGCTAGA | 10277 |
rs371698194 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119523 | TTCAGATGTGCAGCC[A/C]GCCAGCAGTCAGCCA | 10277 |
rs371708780 | snp | C/G/T | 0.000115336 | 0.00759316 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137071 | ATTTTTCCTAGATGG[C/G/T]GATCAGCCTCCATTT | 10277 |
rs371739995 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083824 | AATTGGACTGGCCTT[C/T]GGGCCCCCAAAGGGG | 10277 |
rs371742248 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180022 | AGCAGAAGCAGCGGC[C/T]GCAGCGAAGCTGCCG | 10277 |
rs371772099 | in-del | -/TAC | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10038473 | TTATAATCAAGCAGG[-/TAC]TGTTTTCCTAATTTT | 10277 |
rs371773490 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134557 | ATAAAATGCCTCTTA[C/T]ATAAATAATAATTAT | 10277 |
rs371794066 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075283 | CTAGAGCTTGCTTGG[C/G]CCTGCTCTAGACCTG | 10277 |
rs371831418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134670 | TTGACTTTAGGATAC[A/G]GTTATGTTTGAAAGT | 10277 |
rs371845377 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148802 | AAAATTAGCCAGGTA[C/T]GGTGGCACGTGCCTG | 10277 |
rs371861742 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148226 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 10277 |
rs371915688 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041849 | TTACAGGCACATGCC[A/G]CTACTGCCCGGCTAA | 10277 |
rs371930619 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059491 | GAGCCTTGGGAGGCT[C/G]TCCCGGAAGGGGCCA | 10277 |
rs371939686 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128860 | CTCTAATGTTAGGAT[G/T]GTTGGATGTCTGAAG | 10277 |
rs371947163 | snp | G/T | 1.6615e-05 | 0.00288223 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106415 | CATGGGCGTCCTCAG[G/T]CGTCTCCATTCTGTC | 10277 |
rs371965349 | snp | C/G | 5.3967e-05 | 0.00519429 | intron-variant | UBE4B | GRCh38.p7 | 1:10126749 | TACTTCCCACTCTTA[C/G]ATTCTCTTAAACTTA | 10277 |
rs372009924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10059907 | TACCCAGGAGAGCTG[A/G]GGGGTGGCAACTCTG | 10277 |
rs372027569 | snp | C/T | 1.66302e-05 | 0.00288355 | intron-variant | UBE4B | GRCh38.p7 | 1:10161316 | CAGAGGCTTGGACAG[C/T]TTTGCAGGCCATCTG | 10277 |
rs372027851 | snp | A/C | 3.29598e-05 | 0.00405941 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102990 | GAAGAGCAGGCCTTA[A/C]AGCTGGTCTGTAAGA | 10277 |
rs372057144 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165407 | TTATTGCAGTAGCCC[A/C]CTGCTTGGTCTTCAA | 10277 |
rs372184745 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175405 | GCCTGTAATCCCAGC[A/T]CTTTGGGAGGCCAAG | 10277 |
rs372206719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034631 | CCTCCACATTTCTTC[A/T]CTGGTTCATCATGTA | 10277 |
rs372216045 | snp | A/G | 0.00110869 | 0.0235184 | intron-variant | UBE4B | GRCh38.p7 | 1:10130844 | ACAAATCCAGAGGAA[A/G]TATCAAAGATGAGCT | 10277 |
rs372256101 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131179 | TCTTCAATTCTCAAA[C/T]TTAAAGGCAGAGAAG | 10277 |
rs372260521 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065670 | GGAGTGAAGACGTTA[C/T]GGAGCAGGGCTACAC | 10277 |
rs372287496 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117484 | TCTGGTGGAGCAAGT[A/G]ATTGGGATTCCTACA | 10277 |
rs372288467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080016 | GTGAAGAGGTGCAGA[C/T]GCTGGTGTCCTGTAC | 10277 |
rs372301197 | snp | A/G | 0.000143179 | 0.00845985 | intron-variant | UBE4B | GRCh38.p7 | 1:10168285 | GGTGAGTAGAAACCC[A/G]GGGCTCTGTTTGGTG | 10277 |
rs372328995 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175544 | TAGACCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs372340357 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | UBE4B | GRCh38.p7 | 1:10129494 | TTCAGTGAATATATC[A/G]TAACCCAGAAGGCAT | 10277 |
rs372362624 | in-del | -/GAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060607 | CAAAACAAAACAAAA[-/GAAAA]TAAAAACCTTTCTGG | 10277 |
rs372374032 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166450 | CAGAGAGGCAGACCC[A/G]ATAGGCCTCAATACG | 10277 |
rs372392304 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10113216 | GCAACAGAGAGGAGG[A/G/T]GGATGTCCCAGACTC | 10277 |
rs372394816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10146191 | GCATGGTGGCTCACA[C/G]CAGTAATCCCAGCAC | 10277 |
rs372416371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076703 | AGCTGTAGGGGGTCC[C/T]TCCACTTCCAGTTGC | 10277 |
rs372420989 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10095897 | CTGCCTCAGCCACCT[A/G]AGTAGCTGGGATTAC | 10277 |
rs372443057 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176784 | TCTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs372449456 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118732 | TGGTCTCTAACTCCC[A/G]ACCTCATGTGATCTG | 10277 |
rs372475006 | snp | A/G | 1.68083e-05 | 0.00289894 | intron-variant | UBE4B | GRCh38.p7 | 1:10132486 | GCACAGATGCAGGTA[A/G]GATTCCTACAGACTG | 10277 |
rs372556904 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031839 | TTCATGGTACTGTTA[C/T]TTTGATCGCTCAACT | 10277 |
rs372610659 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071641 | GCCAAGGAGGTGTGA[G/T]AAACAGAGATGGTAA | 10277 |
rs372645590 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053313 | ACCACCATGCCCGGC[C/T]AATTTTTTTGTATTT | 10277 |
rs372658913 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123152 | TAAATCACTGTCGGC[C/T]GGGCGCAGTGGCTCA | 10277 |
rs372659077 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139883 | ACAGGCATGTGCCAC[C/G]ACGCCCAGCTAATTT | 10277 |
rs372667836 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072195 | CATGACCCCAGCTAC[C/T]TCCCCAATAGGTGCA | 10277 |
rs372671422 | snp | A/G | 3.29533e-05 | 0.00405901 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171290 | TATTTACTTACAGCT[A/G]GACTGTGCTCGGTTC | 10277 |
rs372686740 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171516 | TCTGGGAGGCCAAGG[C/T]AGGGGGATTGCTTGA | 10277 |
rs372715295 | snp | A/G | 0.000148247 | 0.00860822 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151440 | GGTGGCCAAACTGGT[A/G]GAAGTCATGTTTATG | 10277 |
rs372767736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111840 | CATGTGCCTATAATC[C/T]CAGCTACTAGAGAGG | 10277 |
rs372781818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128355 | TAACGAGGACACAGT[G/T]AGTGAGAGGGTACAA | 10277 |
rs372786502 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088686 | GTATTTTATTATTTT[A/C]TTATTATTTTTGAGA | 10277 |
rs372810575 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10122111 | CTCTTGCAAATTTTA[A/G]CCTGAGAGCCTCTAT | 10277 |
rs372819662 | snp | C/T | 3.31796e-05 | 0.00407292 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106378 | TCATCCCCGCGGTAT[C/T]GCCCCTACACTGTCA | 10277 |
rs372821008 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045078 | ATGTAGATCCCTCGC[A/G]TGCAGAACTCAATGT | 10277 |
rs372828525 | snp | A/G | 0.000247099 | 0.0111125 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072158 | CAGGACCCTCTCAGA[A/G]TCTTGGTCTCAATGT | 10277 |
rs372876300 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159261 | TCATATACCTACCTG[A/G]AATCTGAGTGACTGC | 10277 |
rs372949804 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10158311 | AACTGGATTTGGAAA[A/G]CAAGAAAATACATAT | 10277 |
rs372963814 | snp | A/C/T | 1.65938e-05 | 0.00288039 | intron-variant | UBE4B | GRCh38.p7 | 1:10179591 | CAGTTTGAGGTGCAG[A/C/T]GCTGGCGTCAGTACC | 10277 |
rs372965293 | in-del | -/AAAT | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10136920 | GCAAAAGTCCATCTC[-/AAAT]AAATAAATAAATAAA | 10277 |
rs372967982 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137436 | CCCTGGATATTTCAC[G/T]CTGTTTATGGTTACT | 10277 |
rs372995397 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10136290 | CCAGCCTGGGCAAAA[A/T]AAGGAAACCCCATGT | 10277 |
rs373028117 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086196 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 10277 |
rs373030845 | snp | C/G/T | 4.94599e-05 | 0.00497272 | intron-variant | UBE4B | GRCh38.p7 | 1:10137231 | TGATACCGTGTCCTG[C/G/T]GATTGCCTGAGTTAC | 10277 |
rs373064775 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120061 | CAACCAAAGTGCTAC[A/G]TTATTTGCTTCTGAG | 10277 |
rs373071786 | snp | A/G | 0.000167986 | 0.00916322 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106204 | TAATTTAGCCTCTAT[A/G]AAAGTAGTCCGGCTC | 10277 |
rs373079835 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058180 | GATTTGGGAGTAAGT[C/G]CTGGACATAGTCATG | 10277 |
rs373085194 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040423 | CTCCGGCTAATTTTT[A/G]TATATTTTGTAGAGA | 10277 |
rs373089029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082299 | AACCCAGGGGTTTAA[A/G]ACTAGCCTGGACAAC | 10277 |
rs373093217 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063114 | CTCTAATAAAAATAC[A/C]AAAATTAGCTGGGTG | 10277 |
rs373123755 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130586 | TTACTTAGGGGCTTT[C/G]TTTAGCTTCTCAGTC | 10277 |
rs373141947 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061696 | CCAGGATTTGGACCC[A/C]TGCCCCAGGTATTCT | 10277 |
rs373178187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051491 | TTACTAGTTAAGGTA[A/G]CAAATAGACCGTGGC | 10277 |
rs373180782 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | UBE4B | GRCh38.p7 | 1:10150977 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 10277 |
rs373201711 | snp | C/G | 6.71659e-05 | 0.00579469 | intron-variant | UBE4B | GRCh38.p7 | 1:10151565 | AGTTTTATACAGGTA[C/G]GTTGCTGGAACACAG | 10277 |
rs373261840 | in-del | -/ACA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073744 | ACAACAACAACAACA[-/ACA]TCAAATTCATGATCA | 10277 |
rs373283041 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086860 | ACGCCCGGCTAATTT[G/T]TGTAATTTTAGTAGA | 10277 |
rs373283238 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056323 | AGCCTAAGAGGAAGA[C/T]TAAAAGAGCAAAGGG | 10277 |
rs373306020 | snp | C/T | 8.20513e-05 | 0.0064046 | intron-variant | UBE4B | GRCh38.p7 | 1:10144929 | ATTTGACTGTTAGTC[C/T]TTGATTTCAGAACTG | 10277 |
rs373309448 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162330 | AGGCACCTGCCACTA[C/T]GCCTGGCTTATTTTT | 10277 |
rs373314655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10123877 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTTAG | 10277 |
rs373349574 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10129886 | TCGAACTACTGACCT[C/T]AGGTGATCCACCCGC | 10277 |
rs373363734 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061000 | ATCCTCCCACCTTGG[C/T]TTCCCAAAATGCTAG | 10277 |
rs373446842 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057439 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTGTCTGT | 10277 |
rs373471616 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054235 | GCTGTTTTCTAACCA[A/G]TTGAGTAATTTGTTG | 10277 |
rs373471735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098410 | TAAACTCACAGTGTG[A/G]CACAGACAAAGTTCA | 10277 |
rs373478102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100101 | TTCAGGCCATTCTCC[C/T]GCCTCGGCCTCCTGA | 10277 |
rs373493148 | snp | C/T | 0.000186891 | 0.00966493 | intron-variant | UBE4B | GRCh38.p7 | 1:10106596 | TAGGTATTTATCCCA[C/T]AGGAGAGTTGCATGT | 10277 |
rs373520300 | snp | C/T | 8.27123e-05 | 0.00643034 | intron-variant | UBE4B | GRCh38.p7 | 1:10119630 | TATGAAGACCCGTGA[C/T]GTGCTTGACATTAGC | 10277 |
rs373543843 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046275 | TATACGTTCTCTCAC[A/G]TCAGAAAGGGAGAGC | 10277 |
rs373572637 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10154706 | ATTTAGCTGGGCGTA[A/G]TGGTGCACACCTATA | 10277 |
rs373582767 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10092376 | ACTACAGGTGCATGC[C/T]GCCACGCCCAGCTAA | 10277 |
rs373583935 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131743 | GGATCACGAGGTCAG[C/T]AGTTTGAGACCAGCC | 10277 |
rs373592173 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140706 | TTTCCAGAGACATTT[A/G]TGTTCACCTCATCTG | 10277 |
rs373592498 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031326 | TCTTGATCCACCCGC[C/T]TTGGCCTCCCAAAGG | 10277 |
rs373594185 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073162 | CTGATGGTCTTCTGG[G/T]AGGATTGATGGGTTC | 10277 |
rs373656730 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050329 | CGCCTGCCTTGGCCT[C/T]CCAAAGTGTTGGGAT | 10277 |
rs373673234 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133739 | ACATAATGAGACCCC[-/C]ATCTCTACAAAATAT | 10277 |
rs373684701 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093975 | GCTGAGATTACAGGC[A/G]TGAGCCATCGTGCCC | 10277 |
rs373702532 | snp | A/C/G | 1.66252e-05 | 0.00288311 | intron-variant | UBE4B | GRCh38.p7 | 1:10168124 | ACTCAGCGTCTGTTC[A/C/G]ATGTGTCCTAGGATC | 10277 |
rs373722567 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153243 | GGGCACGGTGACTCC[A/C]GCTAATAATCCTAGC | 10277 |
rs373722773 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068065 | ATGGAGTCTTGCTCT[G/T]TTGCCCAGGTTGGAG | 10277 |
rs373727252 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057858 | GAAAGTTCTCAAGGA[C/G]GAGGAAGGTGACTTG | 10277 |
rs373742638 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127111 | ACAGGAGTTAAATGC[A/G]CTTATTACAATGTAC | 10277 |
rs373793372 | snp | C/G/T | 0.00358923 | 0.042236 | intron-variant | UBE4B | GRCh38.p7 | 1:10175389 | GGGTGCAGTGGCTCA[C/G/T]GCCTGTAATCCCAGC | 10277 |
rs373796395 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126848 | AAAGAGTGCTCCCTC[A/G]ACAGTGACTACTTTA | 10277 |
rs373827083 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10068646 | ATGAGCCACTGTGCC[C/T]GGCCAGTTTTTGTAT | 10277 |
rs373828728 | in-del | -/AT | 0.0704125 | 0.17392 | intron-variant | UBE4B | GRCh38.p7 | 1:10177658 | AGACTCTGTCTCAAA[-/AT]ATATATATATATATT | 10277 |
rs373850516 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159684 | AGTGAGACTCCGTCT[C/T]AAATAAATAAATAAA | 10277 |
rs373850945 | in-del | -/TTACTATGTTGGC | 0.0998734 | 0.199905 | intron-variant | UBE4B | GRCh38.p7 | 1:10044778 | GATAGAGATAGAGTT[-/TTACTATGTTGGC]CAGGCTGTTCTTGAA | 10277 |
rs373856925 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052023 | GCATATTGCTTCTTT[A/G]TTCCCTGTCAGTGCT | 10277 |
rs373935734 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086003 | TTGAGACAGAGTCTC[G/T]CTCTGTCTCCCAGGC | 10277 |
rs373965454 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076243 | AGTGCTTCTTTCTTT[C/T]TTTCTTTTTTTTTTT | 10277 |
rs373977149 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069800 | CGGACTCCCCTCGGC[C/T]GATGATTTCATCCCC | 10277 |
rs373988095 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10131125 | GTTAGTTTGCACACA[-/C]CCTCACTGACTTGCT | 10277 |
rs373990359 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083104 | ATTGTAAATAGTGCT[A/C/G]TCGTGTACATGTGTC | 10277 |
rs374006800 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164862 | TTGGAATTTTGAGCC[C/T]AGTGGAATTTGGTAT | 10277 |
rs374008598 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172941 | CCGACAGGATTCAGT[A/G]CAGTCCCACACTGTA | 10277 |
rs374031649 | in-del | -/CAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039101 | ACACAGAAAAACAAA[-/CAAA]AAAGCAATTATAATT | 10277 |
rs374076078 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10150665 | AAAAGATCAAGACCA[G/T]CCTGGCCAACATGGT | 10277 |
rs374079816 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10042652 | ACTGTGTCTCAAAAG[C/G]AAAGAAACAAACAAA | 10277 |
rs374081035 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125694 | TCCCAACCAACTCCC[A/T]AAATGTGTTGATCAG | 10277 |
rs374105220 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077897 | CCAGATATTTCTTCA[G/T]GTTTTACTGCATTGT | 10277 |
rs374151375 | snp | C/T | 0.000115631 | 0.00760276 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179967 | ACTAAACCGTTCCGC[C/T]GCCCACCCTCTGCTA | 10277 |
rs374276313 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10137050 | TTTTATTTAGGGAAT[A/G]ATGTTATTTTTCCTA | 10277 |
rs374288783 | snp | C/T | 0.000347438 | 0.0131757 | intron-variant | UBE4B | GRCh38.p7 | 1:10161294 | TGCCCCGGGTGAGGA[C/T]GTGGTCCAGAGGCTT | 10277 |
rs374322231 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081994 | TGTTGGGACTACAGG[C/T]GTGAGCCACTGTTCC | 10277 |
rs374338459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142976 | AGCCAGGCATGGTAA[C/T]GCACCCCTGTAGTCG | 10277 |
rs374345595 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113832 | AGCCCTTTGGGAGGC[C/T]GAAATGGGTAGATCA | 10277 |
rs374391496 | snp | C/G | 1.80041e-05 | 0.00300029 | intron-variant | UBE4B | GRCh38.p7 | 1:10134971 | TTAAAAATACTTTTT[C/G]TTTTCAACTTTCACA | 10277 |
rs374402756 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10179852 | TCTCTCAGGAAGAGC[C/T]CTCCCATCTGGGGCA | 10277 |
rs374433845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10123338 | TGGGAGGCTGAGGTA[A/G]GAGAATTGCTTGAAC | 10277 |
rs374441921 | snp | A/T | 9.99117e-05 | 0.00706724 | intron-variant | UBE4B | GRCh38.p7 | 1:10102912 | TAACTCATACCTCTT[A/T]TTTGAAATTAACCTG | 10277 |
rs374459182 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094830 | GAGTCTCGCTCTGTC[A/T]CCTAGGCTGGAGTGC | 10277 |
rs374463484 | snp | A/G | 0.000201324 | 0.010031 | intron-variant | UBE4B | GRCh38.p7 | 1:10135209 | CTGTGTTCGTGACTC[A/G]GTCATTAAAACACTG | 10277 |
rs374492131 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10175468 | CGTCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 10277 |
rs374551590 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114079 | CAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAAAAA | 10277 |
rs374560124 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050721 | TTCAGGACTCCTATT[-/C]TTTTTTTTTTTTTTT | 10277 |
rs374628108 | snp | A/G | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178764 | GTGGAGGAGATAGTG[A/G]CCAAGAACGCACGCG | 10277 |
rs374634808 | snp | A/G | 6.5962e-05 | 0.00574253 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101064 | CAGTGACATTGTGCG[A/G]ATTTATAAAAGGTAA | 10277 |
rs374640200 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130751 | TTCTCAGGGCCTGCC[A/G]TTACCCTGGAAAACA | 10277 |
rs374654837 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180023 | GCAGAAGCAGCGGCC[A/G]CAGCGAAGCTGCCGT | 10277 |
rs374669012 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135476 | GGGCATGGTGGCACA[C/T]GCCTGTAATCCCAGC | 10277 |
rs374677993 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097724 | CTGAGGCAGGAGAGT[C/T]GCTTGAACTTGGGAG | 10277 |
rs374692148 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101182 | GAAGAGAAAAGCGGA[A/G]CCTCAGTGATAAGGT | 10277 |
rs374747507 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10060805 | CACTCTGTTGCCTAG[A/G]CTAGAGTGCAGTGGT | 10277 |
rs374763737 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | UBE4B | GRCh38.p7 | 1:10147115 | CTTCTTCCTGTTTCC[C/T]TTGTCCCTCCTTGGC | 10277 |
rs374781344 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075904 | AAAAAATTAGCGGGG[C/T]GTGATGGTGCACACA | 10277 |
rs374799748 | snp | C/G | 9.13801e-05 | 0.00675882 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106567 | AGACGCCCCTCCTCC[C/G]TGAGGATCTCTCCTA | 10277 |
rs374810881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10124212 | TGTTACCCAGGCTGG[A/G]GTGCAGTGGCGCCGT | 10277 |
rs374849377 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112443 | CTCGCTCTGTCTCCC[A/G]GGCTGGAGTGCAGTG | 10277 |
rs374885284 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100782 | TGATCTCGAACTCCT[A/G]ACCTCAGGTGATCCA | 10277 |
rs374909068 | snp | A/G | 0.00019913 | 0.00997625 | intron-variant | UBE4B | GRCh38.p7 | 1:10179592 | AGTTTGAGGTGCAGC[A/G]CTGGCGTCAGTACCA | 10277 |
rs374909425 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102298 | ACCTGGAGTGTTAAC[C/T]TGGTCCTATGGAATT | 10277 |
rs374911454 | in-del | -/CT | 0.0410537 | 0.137264 | intron-variant | UBE4B | GRCh38.p7 | 1:10091565 | TCCTTCCACCTCACC[-/CT]CTCAAGTAGCTAAGA | 10277 |
rs374913045 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10071008 | TTGCCCTCCACCTCC[C/G/T]GAGTTCAAGTGATTC | 10277 |
rs374923917 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084187 | GTCATGTGCCCAAGC[C/T]TAGCAAAGGCACAGG | 10277 |
rs374928144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065524 | GGCCCTGTGACTGTT[G/T]TGGCCAGTTAAATGT | 10277 |
rs374963174 | snp | C/T | 4.96077e-05 | 0.0049801 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179997 | AGACACAGCCAAGGC[C/T]AACGAGGCAAGCAGA | 10277 |
rs374970708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10036570 | AAACTCCTGACCTCA[A/G]GCGATCCTCCCACTT | 10277 |
rs374971203 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106313 | CTGTGCCTTCCACTC[C/T]CCTCAGTCCTCACAG | 10277 |
rs374980911 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131097 | ATTTACACTGTGAGG[A/G]TGAGCAAGGATTGTT | 10277 |
rs375016995 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098687 | AGCAAGAACTAAATC[C/T]TTACAGTGTTAAGCC | 10277 |
rs375049780 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032275 | GTGTACAATTCAGTG[A/C]TTTGGGTCTCTCATC | 10277 |
rs375093745 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062859 | GACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCTT | 10277 |
rs375145817 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10107707 | CTCAGACTCCCAAGT[A/T]GCTGGGATTACAGGC | 10277 |
rs375146959 | snp | G/T | 0.000214262 | 0.0103482 | intron-variant | UBE4B | GRCh38.p7 | 1:10129463 | GGTAAGCACTCACCT[G/T]ATGGGCTTGCACATT | 10277 |
rs375183552 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072140 | CCATAGCGGCATCAG[C/T]CCCAGGACCCTCTCA | 10277 |
rs375217063 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180447 | AAAACAAAAGTAAAC[G/T]CCTTTCCCTGGCCCT | 10277 |
rs375242900 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121303 | GAGGTTGCAGTGAGC[C/T]GAAATTGCGCCACCA | 10277 |
rs375249102 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054301 | ACATTAAATTTGAAT[A/G]GTAAAGACATGGCAT | 10277 |
rs375249164 | snp | A/G | 1.68491e-05 | 0.00290245 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106499 | GCAGTTCCAGACAGA[A/G]GCCCAGCAGCACGGG | 10277 |
rs375253390 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171061 | CCAATTCCTGTTCCT[C/T]CACTGAAATGGGAGT | 10277 |
rs375335781 | snp | G/T | 1.65173e-05 | 0.00287374 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126808 | GATATTTATCCCCAT[G/T]TTACAAGGCCTGGCT | 10277 |
rs375348087 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10161320 | GGCTTGGACAGCTTT[G/T]CAGGCCATCTGCCTC | 10277 |
rs375361226 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089726 | TTTTTTTGAGACGGA[A/G]TCTCACTCTGTCTTC | 10277 |
rs375388782 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111010 | CTCTCTTCTCTCTGT[C/T]TCTCTCTGTCTCTCT | 10277 |
rs375447908 | snp | C/T | 1.71965e-05 | 0.00293222 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033620 | CTCCCGCCGTGGTCT[C/T]GAGAACAGAAGGATC | 10277 |
rs375463229 | in-del | -/ATAGATAG | 0.100944 | 0.200705 | intron-variant | UBE4B | GRCh38.p7 | 1:10126303 | AGACTCCGTCTCAAT[-/ATAGATAG]ATAGATAGATAGATA | 10277 |
rs375472277 | in-del | -/AATA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124737 | GTTCACAGATAAATA[-/AATA]GCAGCTAGAATTTAG | 10277 |
rs375507657 | snp | A/G | 3.35188e-05 | 0.00409369 | intron-variant | UBE4B | GRCh38.p7 | 1:10149155 | CCATAATTTCATTTA[A/G]TAAATTGTCCTTTTT | 10277 |
rs375516955 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066974 | CCCCAAAGAGAAAGT[A/G]TTTCCAATTATTTTT | 10277 |
rs375559982 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10102944 | AAATCTTCTTCTTCA[A/C]CAGGAGCCTTCCTCG | 10277 |
rs375569692 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062562 | AGGAGGTCTGCCCAC[C/T]TTGGCTCCCAAAGTG | 10277 |
rs375573143 | snp | G/T | 0.000303791 | 0.0123208 | intron-variant | UBE4B | GRCh38.p7 | 1:10117617 | TAATATGAAATGGAT[G/T]AACTTAAAAAAAAAA | 10277 |
rs375593438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043946 | GTTACTTTGTATACA[G/T]AGAGGAATGGAAACA | 10277 |
rs375633338 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113415 | ATCCCAACCATATCA[A/G]TCACCAAAACACACT | 10277 |
rs375653687 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10104072 | GCCTTACCTCCTCTT[A/C]TGAAGTATAGATATA | 10277 |
rs375683100 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181595 | GGATGGATCACCTGA[C/T]GTCAGGAATTCGAGA | 10277 |
rs375711137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10080065 | AAATAGTCACTTTCT[C/T]AGGCTCCCGGCTATG | 10277 |
rs375763191 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10112164 | CAGAAGGATGCAGCT[C/T]TGTTTCTATTATGTG | 10277 |
rs375795563 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10166822 | CCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 10277 |
rs375806737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100400 | AGGCACAGTAATAGT[A/G]CATACAGCCTCAAAC | 10277 |
rs375807354 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160082 | TGTAGACCCTGAAGT[A/G]TAGCTTCTTTTTTTC | 10277 |
rs375822020 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10046138 | CCTCTTCATGGCACA[A/G]CTTGAAAGTTGCACA | 10277 |
rs375822197 | snp | C/T | 4.99322e-05 | 0.00499636 | intron-variant | UBE4B | GRCh38.p7 | 1:10130465 | CCCCACCGGCCTGTT[C/T]AGCGGCTTGACTGGC | 10277 |
rs375826130 | snp | A/G | 0.000134944 | 0.00821302 | intron-variant | UBE4B | GRCh38.p7 | 1:10151572 | TACAGGTAGGTTGCT[A/G]GAACACAGTGTAGCA | 10277 |
rs375835979 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE4B | GRCh38.p7 | 1:10132503 | ATTCCTACAGACTGC[C/T]TTTCGCTGTTTGTCA | 10277 |
rs375851484 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106732 | TAGTTTGGTAGGCAC[A/C/G]TACTCTGAGTCCATG | 10277 |
rs375853189 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044338 | AGGATTACAGGTGGG[A/G]GCCACCGCGCCTGGC | 10277 |
rs375872278 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10154412 | TGGATTTGGAGCTAC[A/G]AGACAACAGCTGAAT | 10277 |
rs375904050 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043490 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 10277 |
rs375927615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097330 | AAAATTGTAGTGAAT[A/G]CAGATGTTCAGCTTT | 10277 |
rs375952026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144503 | CACTTTGGGAGGCTG[C/G]GGCAGGCAGACCACA | 10277 |
rs375956063 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151527 | TCCTCTCTCCACCAA[A/G]TTGTTGGTACCTTCC | 10277 |
rs375970794 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10084654 | CTGGGAGTTTTCTTC[A/G]CCATCTCCCTTTAGT | 10277 |
rs376001780 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113142 | TGAGGGCCTCAGAAA[A/G]CTTCCAGTCATGGCA | 10277 |
rs376007292 | snp | A/G | 1.65537e-05 | 0.0028769 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144977 | AATGAAAGCCAATGG[A/G]AAGATTCCCCACTGG | 10277 |
rs376011725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10138644 | TCTTTTACTTTTTTT[C/T]TCATGCCTTAGTGCC | 10277 |
rs376014052 | snp | C/T | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103057 | TCATCTTTCTTTCTT[C/T]TCTTTCTGCACAGTT | 10277 |
rs376036800 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162625 | TTTTTTTTTTTTTTT[-/C]TTTTTTAATTTCAAC | 10277 |
rs376052574 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180328 | TATCCGTTGATTTGA[C/T]TGTGATTAGAGAACC | 10277 |
rs376074360 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148936 | CAGAGTGAGACTCCA[C/T]CTCAGGGGAGAAAAA | 10277 |
rs376085674 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039485 | CCCAGGCTGGAGTGA[A/G]GTGGCATGATCTCGG | 10277 |
rs376105067 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152505 | AAGAGCCTTAAAAAT[A/G]CTTTTATCGGGGCCA | 10277 |
rs376117326 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176070 | CCTATTCACCTCTCC[A/G]GGATATTTCATATAA | 10277 |
rs376129845 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134894 | CAGCCAAGATCACAC[C/T]CCTTCGCTCCAGCCT | 10277 |
rs376136541 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166971 | ACACACACACACACA[-/C]AAAAAAAAAAATTAG | 10277 |
rs376198157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060919 | CAGCTAATTTTTAAA[A/G]TTTTTTTGTAGAGAA | 10277 |
rs376198911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10079831 | ATTTAACTTAAAATT[A/G]TTCTTTAACATGTTG | 10277 |
rs376230427 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119539 | GCCAGCAGTCAGCCA[A/G]CTTCTGAGCAACATC | 10277 |
rs376240719 | snp | G/T | 3.2963e-05 | 0.00405961 | intron-variant | UBE4B | GRCh38.p7 | 1:10130479 | TCAGCGGCTTGACTG[G/T]CTCTTCCATCTTCTG | 10277 |
rs376251769 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10064615 | TCAGTTCCACTCTCT[A/G]TCACCTCGTCTCTTT | 10277 |
rs376271508 | snp | A/G | 1.70278e-05 | 0.00291781 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106215 | CTATGAAAGTAGTCC[A/G]GCTCCCACTCCCAGT | 10277 |
rs376272861 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177438 | GAGGCTTCAGTGAGC[C/T]GAGAGCGTGCCTCTG | 10277 |
rs376312346 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087266 | AACTAGAAATGATGG[A/G]ACTGGGTTCCAGTCC | 10277 |
rs376313914 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124349 | GTATTTTTAGTAGAG[A/G]TGAAGTTTTGTCATG | 10277 |
rs376314980 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153322 | ACCAGCCTGGGCAAC[A/G]TGGCGAGACCCCATC | 10277 |
rs376324463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175390 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs376329499 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159682 | AGAGTGAGACTCCGT[A/C]TCAAATAAATAAATA | 10277 |
rs376342854 | snp | G/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147061 | TCTCATTCAGCTGCT[G/T]CTCCGCATCCTGGAC | 10277 |
rs376349016 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126852 | AGTGCTCCCTCGACA[A/G]TGACTACTTTAAATA | 10277 |
rs376369025 | in-del | -/AATA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133206 | CCTTCCTTGACTAGT[-/AATA]AATAATGAATGAATG | 10277 |
rs376388542 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167832 | TCGACCTCGTGATTC[A/G]CCCACCTTGGCTTCG | 10277 |
rs376394184 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131821 | AGCTGGGCATGGTGG[C/T]GGGTGCCTGTAATCC | 10277 |
rs376409180 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175906 | CATGTAGTACAGTCA[A/C]AGCGTTGCACAGCCA | 10277 |
rs376417619 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058036 | GGGTCTCTGTTACAA[G/T]TAAAGTGGGAGTGCC | 10277 |
rs376425529 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062343 | TTTGAGGTGGAGTCT[C/T]GCTCTGTCGCCCAGG | 10277 |
rs376444317 | snp | C/G | 0.000274647 | 0.0117153 | intron-variant | UBE4B | GRCh38.p7 | 1:10117636 | TTAAAAAAAAAAAAG[C/G]CTAGTTATTTGTTTG | 10277 |
rs376448750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10125746 | AGATGAGCTAGGCTG[A/C]GTAAATCTTACATGG | 10277 |
rs376463617 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162833 | TTCCCGTCTCCGTCC[A/G]TGTGTACCAATGTTT | 10277 |
rs376467688 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10126188 | CCTGTAATCCCAGCT[-/G]GCTCGGGAGGCTGAG | 10277 |
rs376516204 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162645 | TTAATTTCAACTTTT[A/T]TTTTAGATTCAGGGG | 10277 |
rs376526081 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110516 | AAAATAAAAGTTAAT[A/C/G]AAAATCAATAAATCA | 10277 |
rs376530455 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067485 | GGTTAATGTTAAAAA[A/C]GTCAAGTAAACAATG | 10277 |
rs376582075 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072181 | CTCAATGTCCACAAC[A/G]TGACCCCAGCTACCT | 10277 |
rs376585441 | in-del | -/TTTG | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10041694 | AGCCCCAGTGGACTT[-/TTTG]TTTGTTTGTTTGTTT | 10277 |
rs376640535 | snp | A/G | 1.69172e-05 | 0.00290832 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033676 | GAGGAAAGCGATGGA[A/G]GAGCTGAGCGCTGAT | 10277 |
rs376660032 | snp | A/G | 0.000302069 | 0.0122859 | intron-variant | UBE4B | GRCh38.p7 | 1:10168102 | CTGATGACCAGGACC[A/G]AGCCTTACTCAGCGT | 10277 |
rs376681874 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156831 | TTAAATAGCTGTTTC[C/G]TTTTTTGGTCACACA | 10277 |
rs376684472 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094494 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCAC | 10277 |
rs376689685 | in-del | -/CAAAC | 0.0185938 | 0.0946107 | intron-variant | UBE4B | GRCh38.p7 | 1:10055945 | CAAAACAAAACAAAA[-/CAAAC]CCAGAAGTAGAAGTA | 10277 |
rs376709333 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166849 | AGAATGGCTCGAACC[C/T]GGGAGGCAGAGATTG | 10277 |
rs376726818 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076511 | GGCCTCCCAAAATGC[C/T]GAGATTACACACGTG | 10277 |
rs376728282 | snp | A/G | 0.000117443 | 0.00766209 | intron-variant | UBE4B | GRCh38.p7 | 1:10119664 | CAGAGAGCCCTAGCC[A/G]TCAGTGGACATCAGG | 10277 |
rs376741973 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10175418 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 10277 |
rs376765074 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068902 | CTGCATGGCTCTTCC[C/T]AAATTTTCCAGCGGA | 10277 |
rs376787652 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035240 | TTGACCTCGTGATGC[A/C]CCCGCCTCAGCCTCC | 10277 |
rs376791603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147509 | ACCCAAAAAAAAAGA[C/T]AATTCACTTCTCAGT | 10277 |
rs376795512 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052953 | ACTGTGTCCTCACTT[A/G]GAGGAAGGAGCAAAG | 10277 |
rs376807921 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116444 | TACCATACCCGGCCA[C/T]ATTACCATCCTTTAT | 10277 |
rs376848883 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114805 | GAAGGCGGAGTTTGC[A/C]CTGAGCAGAGATCAC | 10277 |
rs376879441 | in-del | -/A | 0.323492 | 0.238954 | intron-variant | UBE4B | GRCh38.p7 | 1:10175496 | CTCTACTAAAAATAC[-/A]AAAAATTAGCCAGGC | 10277 |
rs376899578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10056035 | GAATGGAGACCATAC[C/T]ATCCACTTCTATCCC | 10277 |
rs376908926 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049483 | GACGCAATGATGCAT[A/G]CCTGCAATCCCTGCT | 10277 |
rs376914512 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123342 | AGGCTGAGGTAGGAG[A/T]ATTGCTTGAACCAAG | 10277 |
rs376915900 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071053 | CTGGGATTACAGGCA[C/T]GCATCACCACACCTG | 10277 |
rs376919111 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047089 | TGCCATTCTTCCATC[C/G]TACAGTATCTGTGCC | 10277 |
rs376925967 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111816 | ACAAAAATTAGCTAG[A/G]CATGATGGCATGTGC | 10277 |
rs377001392 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161263 | GAGATGAAGAACAAA[C/G]AACAGTGGGACCAGT | 10277 |
rs377002186 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078076 | ATGCAGTGGCACGAT[C/G]TTGGCTCACTGCAAC | 10277 |
rs377005063 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152861 | AGTAGCCATCTTCTA[A/T]CCCTCAGTCTGGGGA | 10277 |
rs377012211 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048146 | GAGCCACTGCATCCG[C/T]CCTGAATGCGTTTTG | 10277 |
rs377036893 | snp | A/G | 2.46381e-05 | 0.00350977 | intron-variant | UBE4B | GRCh38.p7 | 1:10144900 | GGGTAAGATGGATCC[A/G]GCTGTTTTCTTTCAT | 10277 |
rs377064938 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106097 | TATACTTGAACTGAA[A/G]TGATTCTCCTTTAAA | 10277 |
rs377068617 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075899 | TCTACAAAAAATTAG[C/T]GGGGCGTGATGGTGC | 10277 |
rs377088763 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10053747 | GTGCAGGAGTGCAGT[C/G]GCGTGATCACGGCTC | 10277 |
rs377095783 | snp | A/G | 0.000148279 | 0.00860914 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105524 | CCAACAGTATTCTCC[A/G]ATTTTAAGGACTTGA | 10277 |
rs377096262 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10145649 | CTCCTTCCCTGCCTT[A/T]TGCAGGGCCCTCCTC | 10277 |
rs377106861 | snp | A/G | 0.00013217 | 0.0081282 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179968 | CTAAACCGTTCCGCC[A/G]CCCACCCTCTGCTAG | 10277 |
rs377196706 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137193 | GACTCCGGGCTATCC[A/G]GGAGCTCAATAGGTA | 10277 |
rs377228104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059013 | AGCACTTTGGGAGGC[A/C]GGGGCGGGCGGATCA | 10277 |
rs377236741 | in-del | -/AA | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10098167 | TCTTATATTTCAATT[-/AA]GTTTGCTTTAAAATA | 10277 |
rs377287651 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10132313 | TCGTGAAGTCAAAAA[A/G]GAATCATGTGCAAAA | 10277 |
rs377307699 | in-del | -/ATAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126302 | AGACTCCGTCTCAAT[-/ATAG]ATAGATAGATAGATA | 10277 |
rs377331546 | snp | C/G/T | 0.000115395 | 0.0075951 | intron-variant | UBE4B | GRCh38.p7 | 1:10137234 | TACCGTGTCCTGGGA[C/G/T]TGCCTGAGTTACCAC | 10277 |
rs377349325 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102553 | GTAGCTCCGAGTAGC[C/T]AGGCCCGCAACCGCG | 10277 |
rs377359894 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111018 | TCTCTGTCTCTCTCT[G/T]TCTCTCTCTGTCTTT | 10277 |
rs377384327 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064157 | CCCAATCTCTGCCGG[C/T]GCTCCTTTGTTCCTC | 10277 |
rs377409358 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032316 | TTCAAATTTTACCAA[C/T]ACTTTTTGAACACAC | 10277 |
rs377423949 | snp | A/T | 0.000182287 | 0.00954516 | intron-variant | UBE4B | GRCh38.p7 | 1:10072230 | GTAAGCCCAAGCTTC[A/T]TACCTGGGACTCTTT | 10277 |
rs377457479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10067109 | CAAACTGCTAAAAAT[A/G]AGAGGAACAGTTTGG | 10277 |
rs377462667 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081218 | CAGGCCTGTGCCACC[A/G]TGCCTGGCTAATTTT | 10277 |
rs377464768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094590 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT | 10277 |
rs377501335 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120875 | AATAAAAATTCACAA[A/G]CATAACATTACATTT | 10277 |
rs377505339 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157755 | GCACTCCAGCCTGGC[A/G]ACAGAGCGGGACTCT | 10277 |
rs377519264 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100419 | ACAGCCTCAAACTTC[C/T]GGGCTAAAGTGATCC | 10277 |
rs377525871 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070127 | AAAAAATTAAAAATT[A/C]GGTGGGTGTGGTGGT | 10277 |
rs377563587 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126109 | TTCGAAACCAGCGTG[A/G]CCAACAAAGTGAAAC | 10277 |
rs377645162 | snp | C/T | 3.42977e-05 | 0.00414097 | intron-variant | UBE4B | GRCh38.p7 | 1:10178833 | GGCAAGTGGACTCGT[C/T]GTTTTCATGCTGATT | 10277 |
rs377739532 | snp | C/T | 8.31262e-05 | 0.00644641 | intron-variant | UBE4B | GRCh38.p7 | 1:10179890 | TCCTTTTTTTCTTTT[C/T]TCAGTGCCAGAACTG | 10277 |
rs377756764 | snp | A/C/T | 0.000169009 | 0.00919118 | intron-variant | UBE4B | GRCh38.p7 | 1:10103130 | TTACTGCAGAGTACT[A/C/T]GACAAGAAAATAAGA | 10277 |
rs386628378 | multinucleotide-polymorphism | CT/GC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080604 | GCTGAAGAGATACCT[CT/GC]ACTCATGTTCATTGC | 10277 |
rs386628379 | in-del | A/TG | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099236 | GACAGAGCAAGACTC[A/TG]TCTAAAAAAGAAAAA | 10277 |
rs386628380 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135474 | CTGGGCATGGTGGCA[CA/TG]CGCCTGTAATCCCAG | 10277 |
rs397688632 | in-del | -/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10041303 | CTCTAAAACAAGACT[-/T]AACCTCAGCCAACTG | 10277 |
rs397714098 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103616 | TTTGTAGTTTTTTTT[-/T]GTTTGTTTTGTTTTT | 10277 |
rs397775464 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062566 | GTCTGCCCACCTTGG[-/G]CTCCCAAAGTGTTGG | 10277 |
rs397860858 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181079 | ATTTCCTTTGGGGTA[-/A]AAAAAAAAAAAGGAT | 10277 |
rs397934444 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123453 | AAAAAAAAAAAAAAA[-/A]TTACTGTCTTGGAAG | 10277 |
rs397979173 | in-del | -/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10039611 | TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAAAG | 10277 |
rs397979175 | in-del | -/A | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181090 | GGTAAAAAAAAAAAA[-/A]GGATTTGAAACCATA | 10277 |
rs398073777 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062565 | GGTCTGCCCACCTTG[-/G]GCTCCCAAAGTGTTG | 10277 |
rs398102435 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035000 | TGTGGGTTTTTTTTT[-/T]GTTTGTTTGTTTTTT | 10277 |
rs527265507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103872 | ATCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 10277 |
rs527279348 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10111817 | CAAAAATTAGCTAGG[C/T]ATGATGGCATGTGCC | 10277 |
rs527281896 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043542 | CACCATTTTCCTGCC[C/T]CAGCCTCCCAAGTAG | 10277 |
rs527284240 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046172 | CACTCCTGTTTACCT[C/T]TCACTGGCTGGAACC | 10277 |
rs527300422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10096507 | GAGGCCGAGGCAGGT[A/G]GATCACTTGAGGTCA | 10277 |
rs527315170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154350 | TTGAACCCGGGAGGT[A/G]GAGGTTGTAGTTAGC | 10277 |
rs527327790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059817 | TTAGGCATTTTTTTT[C/T]CCACTCCTTTCACAC | 10277 |
rs527362869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10044346 | AGGTGGGAGCCACCG[C/T]GCCTGGCCCAGTTCC | 10277 |
rs527386406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148003 | GAGGCCAGGGCGGGT[A/G]GATCACATGGTCAGG | 10277 |
rs527391299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141702 | GGTTCTGGAAGCGAA[G/T]AGGGATGATGGGTTA | 10277 |
rs527414406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10044866 | GGGATTACAGGCATG[A/G]GCCACCGCGCCTGGC | 10277 |
rs527471512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174804 | CCATAAGCTGATTAG[C/G]GGCCTGCTTACTTGA | 10277 |
rs527480322 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10102135 | AAAAATAAGAAGTTG[C/T]ACTGTAGCCTCCTAG | 10277 |
rs527494411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118508 | ACACCCAGCTAATTT[A/T]TTTTTTTTCTTTTGA | 10277 |
rs527498645 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105320 | ATATAACCATGGTAC[A/G]TTTGTCAAAACTAAG | 10277 |
rs527522171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168051 | ATGTTGGGTTTATCA[C/T]GCACTTTCCAGTTAT | 10277 |
rs527533640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160770 | CTGGCAACATAACAA[G/T]TCCCTGTCTCTACAA | 10277 |
rs527576220 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10036507 | TTTAAAAAATCTTTT[C/T]TTTTTTTGTAGAGAC | 10277 |
rs527599497 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10153731 | GAGGTGGGTGGATCA[C/G]AAGGTCAAGAGATCG | 10277 |
rs527628601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111356 | CTTTGCACGTAATAC[C/T]CCCTCCTGCCTTAGG | 10277 |
rs527657678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120181 | TTAAAAAGGATGTGT[A/G]TTTCATTTCTTTTAT | 10277 |
rs527668173 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156548 | GAGATACATATTGCT[A/G]CATAATAAATTAACA | 10277 |
rs527694919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113078 | AGGTTTAATTGGCTC[A/G]TGGTACCTCAGGCTG | 10277 |
rs527694940 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082352 | AAAAAAATACACAAA[G/T]TAGCCAGGCATGGTA | 10277 |
rs527728453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162143 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 10277 |
rs527728519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170383 | GTATAAATCCAGTTA[C/T]TACATTTCATGAAAA | 10277 |
rs527731674 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094346 | ATTTTTTTTTCAATA[C/T]TTTACTATAAAAATT | 10277 |
rs527760541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061136 | CATACTGCAAACCTA[C/T]GGCATACTTACTTGT | 10277 |
rs527767305 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10068838 | AGACCACCCAAGGGC[A/G]TTATCCTCTACTGAG | 10277 |
rs527783082 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094468 | AGACGGAGTCTTGCT[-/C]TGTTGCCCAGGCTGG | 10277 |
rs527797721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061865 | TACTGTGTTGCTATA[C/G]GTGTGTAGTGTGTGC | 10277 |
rs527806916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148756 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 10277 |
rs527831194 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105689 | ACTGGCTCCAATCCA[A/G]GAACAAGCCCCATGT | 10277 |
rs527831944 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10113715 | CTCACATGCTGGCTG[G/T]GGGTGCTGCATCAGA | 10277 |
rs527841274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038725 | GTTTTGCATGAATGC[A/C]TTCATGATGTGATCA | 10277 |
rs527847591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142266 | GTTACCTATAAACTC[C/T]TGTGATACCCGTAGC | 10277 |
rs527855003 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10088912 | TTAACCTCCTGGGCT[A/C]AAGCGATCCTCCCAC | 10277 |
rs527881002 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181104 | AAGGATTTGAAACCA[C/T]AAAGTGTTCTGAAGA | 10277 |
rs527884038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10089924 | GGCCAGGCTGGTCTC[A/G]AACTCCTTGATCCGC | 10277 |
rs527910085 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162452 | TGCTGGGATTACAGG[C/T]GTGAGCCATTGCACC | 10277 |
rs527918584 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10060578 | GAATGTTTATGTATG[G/T]CATTTTCCTTTACCA | 10277 |
rs527918838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10082623 | CTGTAGGTCCTATTA[A/G]GAAGGCGACTTTTTT | 10277 |
rs527953860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175487 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAAAT | 10277 |
rs527954262 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10168870 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 10277 |
rs527955615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074989 | ACAGCTAGCATGCCC[C/T]AAATCAAGCTTTGCT | 10277 |
rs527982931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127508 | TCCTTTCTGTTCTGA[A/G]TTCGCTTATTTGAAA | 10277 |
rs527987414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039147 | AGGAGATAGATAGGA[A/G]TCCAACAGTTATAGA | 10277 |
rs528015609 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031736 | ATGTAGCAAATACAT[C/T]GTAACTCTTAATTCT | 10277 |
rs528017132 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10128285 | TTCAAAAGACAGAGG[C/T]CTCCATTGTGGTAGA | 10277 |
rs528026268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119265 | GGTGTGAGCCACCGC[A/G]CCTGGCCTCTAAGGT | 10277 |
rs528053834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173305 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 10277 |
rs528065770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123918 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 10277 |
rs528066913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070721 | ATTTTGAATGAATGG[A/G]TTAATTTTTCTCTTT | 10277 |
rs528082407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10078571 | CTTCTTAACTGTCTC[A/G]GGTTATTTTATTTTA | 10277 |
rs528104344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10147319 | CCAACATGGCGAAAC[C/T]GTGTCTCTACTAAAA | 10277 |
rs528105644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116166 | CTTTTATTTTAGGAC[A/G]GCGTCTCTCTTTGTC | 10277 |
rs528105909 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130215 | CAGTAGCTGGGATTA[C/T]AGGCGCACACCACCA | 10277 |
rs528107793 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10095996 | GGCTGGTCTCAAACT[C/G]CTGGCCTCAAGAGAT | 10277 |
rs528116231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165726 | TCCCTCAGATTTTCC[A/G]ACTCCTTCAGATATA | 10277 |
rs528119331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071451 | TAATTAGCTGGACAT[A/G]GTGGTTTGCACCTGT | 10277 |
rs528125205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158576 | CTGGGTTCTTGTTGA[C/T]TGTTTGCTTGGTCTC | 10277 |
rs528126435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166355 | GAGGTAAGCGTGCTG[A/G]CAGTTCTGTGGTGTG | 10277 |
rs528165724 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10121378 | AACAAACAACAACAA[A/C]AAAAACATATAATAC | 10277 |
rs528192387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151699 | CTAACCTGTGGCCTG[C/T]AGAGGATGTACTTTT | 10277 |
rs528202959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159102 | TCTACGATGACAGTG[A/T]TAAATGAAGTTGTCA | 10277 |
rs528217077 | in-del | -/A | 0.242622 | 0.249891 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181268 | CTTCTCTTTTGTGGA[-/A]AAAAAAAAAAGGGCA | 10277 |
rs528222466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10108903 | CTGTGTTACCTGTTT[C/T]ACTGTAAATTTTCTG | 10277 |
rs528233432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041931 | AACTCCTGACCTCAA[A/G]TGATCCACCCACCTC | 10277 |
rs528245181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116838 | GGGGTTGAGACTAGA[A/G]CCCACGTCTGGTTAC | 10277 |
rs528281763 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10167168 | TAGAGGGCCGGGCAC[-/G]GTGGCTTACGCCTGT | 10277 |
rs528311266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086189 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGACC | 10277 |
rs528330219 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10077793 | TTAGAAAAAAAGTTA[C/T]TATATAAAATATTTC | 10277 |
rs528347963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086485 | AGGTATGGGGGGACT[C/T]AAAATCCCGTTATAT | 10277 |
rs528351566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10177242 | AAAGAGGTTTAGGCC[A/G]AGCACAGTGGCTCAC | 10277 |
rs528352443 | snp | A/G/T | 4.94176e-05 | 0.00497059 | intron-variant | UBE4B | GRCh38.p7 | 1:10130636 | GTATAGTGGCTACTT[A/G/T]TACTTTGCTGCCCTT | 10277 |
rs528363400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034748 | CTTAGTGTGTTTACT[G/T]AGGGACTGAAATTCT | 10277 |
rs528401985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035287 | CAGGCGTGAGCCACC[G/T]CGCCTGGCCTGTTTT | 10277 |
rs528425598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131354 | TGGCAGCGCGTGCCT[A/G]TAATCCCAGCTACCT | 10277 |
rs528432999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043630 | AGACGGGGTTTCACC[G/T]TGTTAGCCAGGATGG | 10277 |
rs528437526 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10175636 | AGCCTGGGCGACAGA[A/G]CGAGACTCCGTCTCA | 10277 |
rs528445627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059777 | CCGAAGTTGTTGAGC[A/G]TATCTGGAGGCTCCC | 10277 |
rs528463700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087508 | ATCTCAGTTCTGTTT[C/T]CATGATCTTCACAGT | 10277 |
rs528499042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178922 | TTTTAATGGTGTGCT[A/G]GAGCTGCTTTTTGAG | 10277 |
rs528558580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174352 | GAGCTGAGATCGCAC[C/T]GCTGCATTCCAGCCT | 10277 |
rs528564248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132598 | AGTATTGAACAAGGT[A/G]GACGAGCTTCCTGCT | 10277 |
rs528620770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125933 | TCTAATTTAAGTTTA[A/G]TGTAGTAATAATGTT | 10277 |
rs528670742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109530 | CTTATAGGTTCTTAG[C/T]TGATATAAAAAAGAA | 10277 |
rs528671726 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066878 | GCTACCGCACTCCAA[C/G]CTGGGTGACAGAGCA | 10277 |
rs528684200 | in-del | -/ATT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037965 | AGATGGTTGGCTGGG[-/ATT]ATTCCGGGTGTGGTC | 10277 |
rs528713941 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10152163 | CCCAGGGCGGTTGAG[A/G]GAGGAGAATTGCTTG | 10277 |
rs528799913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138746 | GGAAAGCTTTCTATA[C/T]ATCCTCAGTTACCAG | 10277 |
rs528800224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146324 | GGGTGTGGTGGCACA[C/T]GACTGAAATCTCTGC | 10277 |
rs528801461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10043305 | TGAGCCACCGCACCC[A/G]GCCAACTTTCAGTAA | 10277 |
rs528802506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051043 | GACAGGACTTGCTCT[A/G]TGGCCCAGGCTGGAG | 10277 |
rs528811666 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064195 | TAACCCCTACCTGTC[C/G]TGAAAAAGAAACTTA | 10277 |
rs528841753 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10118044 | GCATTCTTTTTTCAA[A/C/T]GTATGACTAAGCAAA | 10277 |
rs528844290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166441 | TTGTAGAGGCAGAGA[C/G]GCAGACCCGATAGGC | 10277 |
rs528888900 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10117757 | CTTAGGATGTGTCGA[G/T]GAACAAAACAGAGAT | 10277 |
rs528903898 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100063 | GGCGCAGTCTTGGCT[C/T]ACTGCGAGCTCTGCC | 10277 |
rs528917439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159783 | CTATACTTGTTAACC[A/G]AATTACTAGTCAATA | 10277 |
rs528919755 | in-del | -/A/AA | 0.311597 | 0.279388 | intron-variant | UBE4B | GRCh38.p7 | 1:10034478 | AAATTAGGTTGTTGT[-/A/AA]AAAAAAAAAAACAAC | 10277 |
rs528931426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10167095 | CGAGATTGTGCCACT[A/G]CACTCTAGCCTGGGT | 10277 |
rs528937764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10152298 | TAATAATAATAATAC[C/T]ACTTTTCACCTGTCA | 10277 |
rs528972344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050160 | CACTGCAACCTCCAC[G/T]TCTGGGGTTCAAGCA | 10277 |
rs529022783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138570 | ATAGTTAACTCTGCA[A/G]ATTCTTTATGATTTA | 10277 |
rs529049705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10035461 | GAGTGCAGTGGCGCT[A/G]TCTCAGCTCACTGCA | 10277 |
rs529073702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177340 | GCCTGGCCAACATGG[C/G]AAAACCCTGTCTCTA | 10277 |
rs529074308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10081572 | TGGGACTCCTGGCAC[A/G]TGCCACCATGCCTGG | 10277 |
rs529085845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10173354 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 10277 |
rs529086618 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048822 | AGGCTCCAGGGGTGC[A/G]CTGGGAAGCCATCTG | 10277 |
rs529095529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178050 | CGTGTCTGTTCCCAG[A/G]CCTATTCATCAGTTC | 10277 |
rs529134302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087284 | TGGGTTCCAGTCCTA[C/G]TTTCTTTGTAAAATG | 10277 |
rs529138233 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10078713 | GAGGTCATGATTGCT[C/T]AAGAGTCCCCCAACA | 10277 |
rs529160186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173799 | ATCACAGGCGCTTAA[C/T]GTAACACACAGAAGG | 10277 |
rs529168834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124003 | TGGTGTTGAATTCCT[A/G]ATGTCAGGTGATCCA | 10277 |
rs529172473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10036074 | TAGTCCTTTACTCCT[A/G]TAAATTACTTTTTTT | 10277 |
rs529199310 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078876 | GGCTGGAGTACAGTG[G/T]TGCGACCATAGCTCA | 10277 |
rs529218297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124667 | GAAAGAGTGGCAAAT[C/G]TGAATTATTAAATCT | 10277 |
rs529236495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037901 | TGGTAATGAGATTGC[A/G]TAAGTGATTTTTCTC | 10277 |
rs529265314 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10092696 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 10277 |
rs529272741 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10060357 | GTAACTATACTGAAT[C/T]CTGTGGGCAGTTGTA | 10277 |
rs529275273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133338 | TTAGACAGTGACTCC[G/T]CTGTGCCTCCATTTC | 10277 |
rs529280963 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057252 | TTAGGCGTGTTTAAC[A/G]TTCTTCATGTTATCA | 10277 |
rs529390892 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10065847 | ACTAATAATAATGTT[A/C]ATTATAATGTAAATC | 10277 |
rs529398338 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116875 | TACAATATTTTTGTT[C/T]TGTCTTTTACTATAC | 10277 |
rs529402623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051119 | TCAGATGATTTTCCC[A/G]CCTCAGCCTCCTGAA | 10277 |
rs529414841 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079320 | TGCGCCACCACGCCC[C/G]GCTAATTTTTTGTAT | 10277 |
rs529419874 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088940 | CACCTCAACCTCTCA[A/G]TGTGTCGGGATTACA | 10277 |
rs529419930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118588 | CGGCTCACCGCAACC[C/T]CTGCCTCCTGGGTTC | 10277 |
rs529437970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127154 | ATGAAAAAGATAACT[C/T]ATCTCCTAGCAATGA | 10277 |
rs529457959 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119988 | CTTCCATGTATAACA[C/T]GGTCAATTTCTGTTA | 10277 |
rs529503429 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062956 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs529551195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088357 | CAGACTTGAAATGTC[A/G]TTTTATTTTATTTGT | 10277 |
rs529566302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140708 | TCCAGAGACATTTAT[A/G]TTCACCTCATCTGTG | 10277 |
rs529588559 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144338 | TTCCCTCCCAGAAAA[A/G]TAAGGGAACAATGTA | 10277 |
rs529600216 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10167444 | CTCCGTCTCAAAAAA[A/T]AATAATAATAATAAT | 10277 |
rs529617786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10037192 | GCCACCATACCCGGC[A/T]AATTTTGTATTTTTA | 10277 |
rs529621044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132854 | GAAAAGAGCTATCCA[A/G]TGTGGAAACGAAGCA | 10277 |
rs529646569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070454 | AATTAAAAAAAAAAA[A/C]AAAAAACCATTACCA | 10277 |
rs529674447 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032864 | GCGGGGAGAGGACGC[A/C]GGCGAGAGGAACTCG | 10277 |
rs529684128 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104344 | AGTAGTCATTTGGAA[C/T]GCAGAAGAGGTATGG | 10277 |
rs529690242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175621 | GCGCCACTGCACTCC[A/C]GCCTGGGCGACAGAG | 10277 |
rs529768219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176455 | CATTTGACATTCCCA[A/C]TGGCAATGTATAAGG | 10277 |
rs529783529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10122170 | CTTTTGCCTGAATTC[A/G]AACATCCATGTGTTA | 10277 |
rs529792142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154877 | GTAGGGAAGGACATA[C/T]ACCAAAATAGTAACA | 10277 |
rs529813234 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033495 | GTGACCGAAGCCAAG[A/G]CAGTTTAGTGCCTCT | 10277 |
rs529876335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149529 | AATTGAGTTGAATTT[C/G]TAATAGTTAAATATG | 10277 |
rs529918041 | in-del | -/TATAAT | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099531 | ATGAAAACTCAGTAA[-/TATAAT]TATATTACTTCTCCC | 10277 |
rs529925274 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175411 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 10277 |
rs529929673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046854 | TTGATTGTAGACCGC[G/T]GACATTCCTCAGGCA | 10277 |
rs529932793 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175532 | GGCGGGCGCCCGTAG[A/T]CCCAGCTACTCGGGA | 10277 |
rs529966687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040228 | CCCCTGGGTTCAAGT[C/G]ATTCTCCTGCCTCAG | 10277 |
rs530003081 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121128 | CCAGCACTTTGGGAG[C/G]CCAAGGCAGGTGGAT | 10277 |
rs530008628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142833 | ATAGTATCTTTAGAT[C/T]TCCTTCGCTTGCCTG | 10277 |
rs530020168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108634 | CAGTAGGAGTTAGGT[A/G]CACTTCATTCAATTC | 10277 |
rs530020683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143585 | TACCCTTAATCACAT[C/G]TACAACGTCCCTTTC | 10277 |
rs530021031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10135677 | GGAGGCTGAGCTTGC[A/G]GTGAGCCATGATCAC | 10277 |
rs530023240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047632 | CGAGTAGCTGGGACT[A/G]CAGGTGCCCGCCACC | 10277 |
rs530070658 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137683 | CAGATAGCAGCCTCA[A/G]ATTTCCAATTCATTA | 10277 |
rs530070705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056468 | GGTACTGTCATAGTT[G/T]CTGGGAATACAGCGG | 10277 |
rs530084820 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103735 | TCCTGGGTTCAAGCA[A/G]TTCTCCAGCCTCAGC | 10277 |
rs530126256 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10101425 | TGGTTCAGGGCCATG[A/C]TTTTATCAGTAAATT | 10277 |
rs530129601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042012 | CTATCTTGGCTCACT[A/G]CAACCTCTGACTCCT | 10277 |
rs530141460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10138091 | AGATGTGCACCACCA[C/T]GCCTGGCCAATTTTT | 10277 |
rs530143007 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037508 | CATTATATTAATTCT[A/G]TAATCTACTCATGTG | 10277 |
rs530147203 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10109903 | TGATCTGCCCACCTC[A/G]GCCTCCCAGAGTCTC | 10277 |
rs530171673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093970 | AAAGTGCTGAGATTA[C/T]AGGCGTGAGCCATCG | 10277 |
rs530207273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144819 | AGATATACTCTGATT[A/T]TAAAGATGTTACAAT | 10277 |
rs530256142 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136101 | ACATAATTTAATACC[A/G]TTTCGAGATTTAAAT | 10277 |
rs530348308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150957 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 10277 |
rs530369613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10108172 | GTGTGTGTGTGCGTG[C/T]GTGCTCCCTTCCCAC | 10277 |
rs530382577 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043276 | AGCCTCCCAAAGTGC[C/T]GGGATTACAGGTGTG | 10277 |
rs530435398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055815 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 10277 |
rs530439610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158307 | CAATAACTGGATTTG[A/G]AAAGCAAGAAAATAC | 10277 |
rs530449761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077681 | CTGGCTGACATTGTT[C/G]CTCTCACCACAACCA | 10277 |
rs530481443 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073874 | TACCTCATTCTCCAT[A/G]CTCACTCTCTCAGCT | 10277 |
rs530485379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070509 | TCTCCCGAGCTGCTT[C/T]CTGCCCCTTTCCCAC | 10277 |
rs530493819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034642 | CTTCACTGGTTCATC[A/T]TGTAAACTTCCCTAC | 10277 |
rs530532506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10071337 | CCATAATCCTAGTAC[C/T]CTGGGAGGCCAAGGT | 10277 |
rs530547160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115462 | TTTTAGTTGAGATAG[A/G]GTTTCACCATGTTGG | 10277 |
rs530581870 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10153317 | TGGAGACCAGCCTGG[A/G]CAACATGGCGAGACC | 10277 |
rs530630419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10175519 | AGCCAGGCGTGGTGG[C/T]GGGCGCCCGTAGACC | 10277 |
rs530631752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10092776 | GAGGTTGCTTTGAGC[C/T]GAGATCGTGCCATTG | 10277 |
rs530651477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123842 | GCAATGGCATGATCT[C/T]GGCTCACTGCAACCT | 10277 |
rs530666457 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170482 | ATCTTCCTGTTTCAG[A/G]TTTGCTTAAAACCAT | 10277 |
rs530704100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040975 | GGCCTGAGGACCTGA[A/G]GTCCCTTTTTTCCTC | 10277 |
rs530739302 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10041821 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGGTTA | 10277 |
rs530787196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10093298 | ACCTTGTGATGGTGT[A/G]TTATTTATTCCTTCA | 10277 |
rs530789010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093985 | CAGGCGTGAGCCATC[A/G]TGCCCAGCCAATGGT | 10277 |
rs530793280 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10102175 | GCTTTATTTTGTATA[A/G]TTCTTTAATGTTTAC | 10277 |
rs530798122 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056921 | AGCCTCAGCCTCCCC[A/G]GCCCACCTCAGCCTC | 10277 |
rs530836049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10130014 | TATGGAAAAGTTATT[C/T]GAGTCCTTTGGTGGT | 10277 |
rs530845466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10136948 | AAATAAATAAACAAA[C/T]AAAAAGTATCTTTAA | 10277 |
rs530846230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138221 | TCCTGTCTCAGTCTC[C/T]TGAGTAGCTGGGACT | 10277 |
rs530879882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042524 | TGGTGGTGCACGCCT[A/G]TAATCCTAGCAACTC | 10277 |
rs530900667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035522 | CTGCCTCAGACTCCG[A/G]AGTAGCTGGGACTAC | 10277 |
rs530923420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131989 | GCAAAAACTAGCTGG[A/G]TGTGGCGGCGTGTGC | 10277 |
rs530985508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087329 | ACTAACTTTCAATGT[A/G]CAGAAAAGTTATGAA | 10277 |
rs530993400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178082 | CCAGGGTGGTCTAAC[A/G]TCCATGGAGCCCCTG | 10277 |
rs530998402 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062024 | AAGCTTTTCTTCTGC[C/T]TCAGCTTCCTGAGTA | 10277 |
rs531015831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10043255 | CTCAGGTGATCTGCC[A/G]GCCTCAGCCTCCCAA | 10277 |
rs531064119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036376 | ATTCACTAATACAGG[A/C]TCAATGTAAAATTAT | 10277 |
rs531101161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116061 | CATGTCAATTCCTCT[C/T]GGTCCTGTTAGTTTC | 10277 |
rs531117307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165537 | TCAGAGCCAAATCCT[A/G]TGGTGAGAGCAGCCT | 10277 |
rs531139316 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126630 | TAGACTTGTCAAAGA[A/G]CAGGTCAACACTCTG | 10277 |
rs531152287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101491 | AATTCTTTCTGTTGG[C/T]CTTTTGCTTTTTTTT | 10277 |
rs531172798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064042 | TCGTCATGAGCTTGT[C/T]GCAGCTTGTCTTTCT | 10277 |
rs531190869 | snp | C/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151516 | ATTGAGAACCATCCT[C/G]TCTCCACCAAGTTGT | 10277 |
rs531245856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048947 | CTACTTTCTTTATTC[A/G]TTCAACACTCTGTTT | 10277 |
rs531254128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152122 | AAAAATTAAATTAGC[C/T]GGGCATGGTTGCAGG | 10277 |
rs531280677 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046547 | CCTGCCAGGCTGAGC[A/T]GTGAGCGCTTCCTCC | 10277 |
rs531283512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10045293 | GAGAGGCCGAAATCC[A/G]TAAGTGTGTGAAGCC | 10277 |
rs531287595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053371 | AGCCAGGGTAGTCTC[G/T]ATCTCCTGACCTCGT | 10277 |
rs531315042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097369 | AAAAAAAGACAACAG[C/G]GGTCCAGGATATATC | 10277 |
rs531331670 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10039237 | CCCCGGGAGAGGCAG[A/G]GTCTTAGTGAAGACT | 10277 |
rs531351134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090133 | TGTGTGTGTGTTTTT[G/T]TTTTTAGGCATGGTT | 10277 |
rs531372677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141745 | AAATAGCATTACCCT[A/G]CAAGGTGACTATCTC | 10277 |
rs531372940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119112 | GGCGTCGATCTCCTG[A/C]CCTTGTGATCCGCCC | 10277 |
rs531387696 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162416 | CTGACCTTGTGATCC[A/G]CCTTCCTCGGCCTCC | 10277 |
rs531400324 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074099 | ATGTGCCACCACACC[C/T]AACTCTGGCCTCATA | 10277 |
rs531409905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111849 | ATAATCCCAGCTACT[A/G]GAGAGGCTGAGGCAG | 10277 |
rs531427328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046077 | TTCCATCTTTTGGCC[C/T]TTGTATGTCTGCATT | 10277 |
rs531446147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066610 | ATAAAACCAATAATA[A/G]TACTAGGAGTTATTG | 10277 |
rs531517004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160862 | GCAGGAAGATTGCTT[C/G]AGCCCTGGAGGTCGA | 10277 |
rs531541129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104565 | ATCTTCTGAGGAGGG[A/G]AAAAAAAAGTCCTTT | 10277 |
rs531619606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088558 | TTTTTGTATTTTTAG[C/T]AGAGACGGGGTTTCA | 10277 |
rs531646488 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10061995 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTAAA | 10277 |
rs531650728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156657 | CTCCTGTATCTTCCT[C/T]TTGTAGGCTATCCTT | 10277 |
rs531652819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052631 | TGCTCTGCTGTTGCT[A/G]TCTTGAAATTCTTAA | 10277 |
rs531657823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148095 | AGCTGGGCGCTGTGG[C/T]GGGTGCCTGTAGTCC | 10277 |
rs531706677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046904 | TTTGCATGCGAATTG[A/G]CAAGCTTTGGCTTGA | 10277 |
rs531709810 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10057519 | ACTACTGCACTCAAG[C/T]GCTTCTCCTGCCTGA | 10277 |
rs531748195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053304 | CAGGCATGCACCACC[A/G]TGCCCGGCTAATTTT | 10277 |
rs531767287 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140653 | GGAACCATCTAGAAC[A/C]TTTGCTCCTGGCTTG | 10277 |
rs531775383 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031958 | AGTGGCGCGATCTCG[A/G]CTCACTGCAAGCTCC | 10277 |
rs531775732 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10163587 | GCAGGATAATTGCTT[A/G]AACCCGGGAGGCGGA | 10277 |
rs531809294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062605 | GCGTAAGCCGCTGTA[A/C]CGGCCGCCTTAATGC | 10277 |
rs531828134 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113381 | GGGGACTGCATTTCA[A/G]TGTGAGATTTGGACA | 10277 |
rs531848200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055104 | TTTTACTTTGAACAG[A/G]TGTCCTTGTGCCAAA | 10277 |
rs531856580 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10097511 | GGAGCATTTGAAAGA[-/TAT]TATTTTAAAAAATCA | 10277 |
rs531866812 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10129113 | AATATATCTGAAAAC[C/T]GTTGCTCAAAATATC | 10277 |
rs531880838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170717 | AGGGGCTTTTAACAT[C/T]TATGGGGAAAAAAGT | 10277 |
rs531884019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099661 | AGAGCCAAGGATAGC[A/G]AAACCTCTTAAAGGA | 10277 |
rs531893754 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBE4B | GRCh38.p7 | 1:10041630 | GTGAACGACTGTGCC[C/T]GGCCACATTTATAGC | 10277 |
rs531936067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175504 | AAAATACAAAAAATT[A/G]GCCAGGCGTGGTGGC | 10277 |
rs531939963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169743 | CATAAGGCCAAGCAC[A/G]GTGGCTCATGCCTGT | 10277 |
rs531941228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10121229 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 10277 |
rs531950264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175610 | GAGCCGAGATCGCGC[A/C]ACTGCACTCCAGCCT | 10277 |
rs531957187 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099237 | ACAGAGCAAGACTCT[A/G]TCTAAAAAAGAAAAA | 10277 |
rs531968127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084527 | CATTTGTCTGGTCTT[C/G]CAAACTAGATTGAAA | 10277 |
rs531979154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075553 | AACAGAAAGGCTTGG[G/T]CATTCCCTAAACGGT | 10277 |
rs531997028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091851 | CTCAAGTGATCCACC[C/T]GTCTTGGCCTCTCAA | 10277 |
rs532022599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120365 | GTCTCTACTAAAAAT[A/G]CAAAAGACTTAGCTG | 10277 |
rs532083995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10135592 | AAATACAAAAATTAG[C/T]GGGTGTGGTGGCACG | 10277 |
rs532139066 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10099027 | ACAGATCACTTGAGG[C/T]CAGGAGTTCGAGACA | 10277 |
rs532145846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129175 | GTAATTTTTAGTTTC[A/G]TTTTATATTTCTGTT | 10277 |
rs532148931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083794 | GTGTCCTATGCTGGC[A/G]TGGGTACTTCCTCGA | 10277 |
rs532157442 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101566 | CAGGCTGGAGTGCAG[C/T]GGTGCGATCTCGGCT | 10277 |
rs532170357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112972 | CCCCCCATCTGCCGC[C/G]TTGCAAGTCAGCTTG | 10277 |
rs532209903 | snp | C/T | 3.30273e-05 | 0.00406356 | intron-variant | UBE4B | GRCh38.p7 | 1:10105489 | CGAACTGTGTGTAAC[C/T]TGTTCTTTGTTCTGC | 10277 |
rs532228333 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152657 | ACAAAAATTAGCTGG[A/G]TGTGGCGGGCGGCGC | 10277 |
rs532236617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155029 | AGTTAAATTTATTTT[A/G]TAGTCAGTGTTCTGG | 10277 |
rs532240418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040056 | TTCTAGCTATGGAGA[A/G]GGATAGATAAGGGTT | 10277 |
rs532279553 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032717 | GTCCCTCCCCTTGCC[A/G]GCCTACCTGGCTCAG | 10277 |
rs532292888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053441 | GGCGTGAGCCACTGC[A/G]CCTGGCCTATTTATT | 10277 |
rs532293237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10150899 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCACC | 10277 |
rs532315572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098725 | ATTTCAGAGTGTATG[A/T]GTTACTACAGTATAG | 10277 |
rs532317999 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173661 | CTGACTGTAGCTGGC[A/G]TCTCCAGCCCAGCCA | 10277 |
rs532354785 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127423 | CATTGTGGACAGAAG[C/T]TTCAGCTAGATTCCC | 10277 |
rs532388194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107271 | GCACTTTCTGGGGAC[A/T]GTAGTGATGAAGAAG | 10277 |
rs532397216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10039368 | GGTGGGTTTTACCTC[A/G]GGTGTGTGGCAGGTA | 10277 |
rs532450520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149409 | TTTTAACTGAATGCT[A/G]CCTAGAGACTGGAAA | 10277 |
rs532457889 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10150936 | GGAGGTCGAGGCGGG[C/T]GGATCACGAGGTCAG | 10277 |
rs532459690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143679 | GCCATTCTTTTGTCT[A/G]CCATACTCATGTTTC | 10277 |
rs532472402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046161 | GTTGCACAGATCACT[C/G]CTGTTTACCTCTCAC | 10277 |
rs532508486 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045222 | CCTCACTCGCGTGCT[A/T]GCTTGGTACTGGTCT | 10277 |
rs532569699 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10157385 | GGGATGCTGAGGTGG[C/G]AGGATCACTTGAGCC | 10277 |
rs532579175 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040749 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAAGCAT | 10277 |
rs532579414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113827 | ATCCTAGCCCTTTGG[C/G]AGGCCGAAATGGGTA | 10277 |
rs532579456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121907 | GACATGACATTTCAC[A/G]TGCCTCTGTAGTGAG | 10277 |
rs532587363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076288 | CTCACTCTGTTGCCT[A/G]GGCTGGAGTGCAATG | 10277 |
rs532591635 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10086132 | GCCCGCCACCACGCC[A/C/T]GGCTAATTTTTTGTA | 10277 |
rs532632816 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175784 | AGAATATGAGTCTGC[A/G]TCTCACAAATGTAAT | 10277 |
rs532647377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163632 | AAGATCGCACCACTG[C/T]ACTCCAGCCTGGGCG | 10277 |
rs532663164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048459 | TTTACCTAGAGAGTG[A/G]GCATAAATGCGGAAG | 10277 |
rs532680011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100774 | GGTCAGGCTGATCTC[A/G]AACTCCTGACCTCAG | 10277 |
rs532690140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129878 | GGCTGGTCTCGAACT[A/G]CTGACCTCAGGTGAT | 10277 |
rs532698874 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155212 | CAGAAGGAATTGGGT[G/T]GGGGTTGTTCTCTCT | 10277 |
rs532716299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10114338 | CAGCAGAGGAGGGAT[C/T]GCAGGTCTTGAAACT | 10277 |
rs532731016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175769 | CTCCTCTAACCTACC[A/G]GAATATGAGTCTGCG | 10277 |
rs532770558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076891 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACGCC | 10277 |
rs532783142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069056 | CTTGATTCTTCAACC[G/T]TTTTTGAAACCTTAG | 10277 |
rs532814052 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038000 | TTTTAGAAAGTGTTG[A/G]CCGGGCGCAGTGGCC | 10277 |
rs532821020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10069754 | TGGCCAGGCTGGTCT[C/T]GAACTCCAGACCTCA | 10277 |
rs532823375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10069692 | GGTGTGTGGCACCAT[A/G]CCTGGCTGATCTTTG | 10277 |
rs532865335 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10147250 | AATCCCAGCACTTTG[A/C/G]GGGAGGCTGAGGCAG | 10277 |
rs532873651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059351 | GGCACCTGCTCTTCT[A/G]TAAGAGTCTGAAGGA | 10277 |
rs532908591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051750 | CTGCATATCAGGACT[A/G]AAGAATACAGCCTGA | 10277 |
rs532915646 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083208 | CTGGTTCTAGAAGAA[C/T]GTGACATTTTTAGCA | 10277 |
rs532916448 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10167897 | CCCGGCAGATGGTGA[-/CTT]CTTTTATCATTGAGG | 10277 |
rs532934991 | snp | A/G | 0.00112644 | 0.0237055 | intron-variant | UBE4B | GRCh38.p7 | 1:10132518 | TTTTCGCTGTTTGTC[A/G]AATTCATTCATCTGA | 10277 |
rs533005957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080510 | ACAATATGGAGGTCC[C/T]TCAGAAAACTAAAAA | 10277 |
rs533022260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10166795 | TCAAGCATGGTGGCA[C/T]GCACGTGTAATCCCA | 10277 |
rs533098186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103803 | CAGCTAATTCTTGTA[C/T]TTTTAGTAGAGACAG | 10277 |
rs533102454 | snp | C/G | 4.94907e-05 | 0.00497422 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095444 | GGGGCTTCATCCTTC[C/G]TGTGTTTTCTGTTTA | 10277 |
rs533132603 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052932 | TTCATAGATACCTGT[G/T]TTCTCACTGTGTCCT | 10277 |
rs533135742 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10175433 | AAGGCGGGCGGATCA[C/T]AAGGTCAGGAGATCG | 10277 |
rs533140058 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063457 | CTAGATTATTCTTCT[C/T]CCTCACTTTTTACTT | 10277 |
rs533141317 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031122 | TTGTGACGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 10277 |
rs533163060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082378 | TGGTAGTGCGCACCT[A/G]TAGGCCCAGCTACTG | 10277 |
rs533189954 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10072593 | ATGAACACCTCTAAT[G/T]GCAGATTTCCTCGTC | 10277 |
rs533195292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168847 | CAGTGAGCCGAGATG[G/T]TGCCACTGCACTCCA | 10277 |
rs533206343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174317 | AGAATAGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 10277 |
rs533223614 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061735 | CCCAGAAATCAAGCC[A/G]CACCAGCAAAGCTGA | 10277 |
rs533225454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066712 | GGAGTTTGAGACCAG[A/C]CTGACCAACAAGGTG | 10277 |
rs533227819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073394 | ACCATTTGAACTAAT[G/T]GAAAACTTTTGAAAT | 10277 |
rs533236155 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064672 | CCCTGGCTAGTCCAT[A/C]TCTGTGCCTACTGTG | 10277 |
rs533310537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044296 | CTGACCTCAAATGAT[C/T]GGCTTGCCTCGGCCT | 10277 |
rs533333182 | in-del | -/TA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081025 | TAAATAATAACGTTT[-/TA]TATATATTTTTTAAA | 10277 |
rs533344923 | snp | G/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031106 | CAGGAGTCTTTTTTT[G/T]TTGTGACGGAGTCTC | 10277 |
rs533359112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10179798 | CAATGAGGGAAAGAA[A/T]GGCCTTTTCTTCCCA | 10277 |
rs533430233 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180248 | CAGTTTGGGGCAACG[A/G]AAGTCTTTTAGTGAT | 10277 |
rs533435461 | in-del | -/T | 0.528937 | 0.181889 | intron-variant | UBE4B | GRCh38.p7 | 1:10072435 | TCCATAACTTCCATC[-/T]TTTTTTTTTTTCAAA | 10277 |
rs533446674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10090308 | TATTTTTCATAGAGA[C/T]GGGGTCTCCCTGTGT | 10277 |
rs533454288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119262 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCTCTAA | 10277 |
rs533473877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038575 | TGGAATTCAAACCCA[G/T]TGCTCTGGACTCGAA | 10277 |
rs533478228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10060068 | CTGTTCTATTCAGTC[A/G]TCAGGTCCCTGTGTG | 10277 |
rs533491136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10120058 | AATCAACCAAAGTGC[C/T]ACATTATTTGCTTCT | 10277 |
rs533494700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10111920 | CAAGATCACACCACT[A/G]CACTCCAGCCTGGGC | 10277 |
rs533533820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140864 | TTTAAGTTTTGAATC[A/G]TTTCCTCTGAATTAG | 10277 |
rs533535598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10095747 | TATTAAATTTAAAGA[C/T]TTTGTATTATTCAGA | 10277 |
rs533547155 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10096334 | TGGTAAGAGTGGCTG[A/G]GGTATTGACTCCTTT | 10277 |
rs533572097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139822 | CAACCTCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 10277 |
rs533584243 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162887 | CTTCTTATGTATTAA[A/G]GTTCTACCCATTCTC | 10277 |
rs533591270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088954 | AATGTGTCGGGATTA[C/T]AGGCGTGAGCCACCA | 10277 |
rs533598793 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10043825 | TGAACCTGGTTATAC[C/G]TGTTCATGTAATCAC | 10277 |
rs533601263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113104 | GGCTGTTCAAGAAGC[A/G]TGACACCAGCATCTG | 10277 |
rs533627256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037545 | TTCGTATCTCAAGGT[A/G]GTGCTGTGAGTAGGT | 10277 |
rs533629923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081625 | TGGAGTTTCGCTCTT[A/G]TCACCTAGGCTGGAG | 10277 |
rs533651774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133575 | ACAATGTCACATGAT[A/G]AGAAGTGGAGCAACT | 10277 |
rs533664751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038007 | AAGTGTTGGCCGGGC[A/G]CAGTGGCCCACGCCT | 10277 |
rs533756050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087775 | TATTTTTCCCTTTCC[A/G]TATTCAGTTCTTTGG | 10277 |
rs533790525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088445 | GCGTGCAGTGGCGCA[A/G]TCTCACTGCAACTTC | 10277 |
rs533795722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146014 | GAAAGTTTACCTGAC[A/G]TAGCTTTCTAGTACC | 10277 |
rs533806718 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10179203 | TCTGTTCCCTCCCCC[A/C/G]AGCAGTAGCTGACAA | 10277 |
rs533831287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081193 | TCAGCCTCCTGAGTA[G/T]CTGGGATTACAGGCC | 10277 |
rs533839261 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105293 | CCCAGTTTCCCCTGA[C/T]GTTAATATCTTATAT | 10277 |
rs533851100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146664 | TGACACCCAAAGGGC[C/T]TCCCTGTCGCCACCC | 10277 |
rs533854989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139209 | GATGCTAGCCTGGCC[A/T]ACATAGTGAAAACCC | 10277 |
rs533855463 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041364 | TTTTTGATGGAGTTT[C/T]GCTCTCGTCACTCAG | 10277 |
rs533879571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132997 | GTGATCAGAACTGTC[A/G]TGGGAGGGTTTTCAG | 10277 |
rs533907006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126047 | AGCTCATGCCTGTGA[A/T]CCCAGCACTTTGGGA | 10277 |
rs533923444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174626 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 10277 |
rs533941719 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035413 | TTTTTTTTTTTTTTT[-/TT]GAGGCGGAGTCTCGC | 10277 |
rs533974795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060316 | TGGCCTAGGTATTGC[C/T]CCTGGGCTACAAACC | 10277 |
rs533974880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10052233 | CACCATACCTGGCTG[A/G]TTTTTTAATTTTTTT | 10277 |
rs533995416 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10148257 | GTGTGTAGCTCTGTT[G/T]TTTCCGTTTGAGTTG | 10277 |
rs534050298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045512 | ATTTTGTTTCTCTTG[A/G]TGGTGAAAAATAATG | 10277 |
rs534073109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050631 | ATCCAAGTTCTGGCA[C/G]AGGGCTTGGCACAGA | 10277 |
rs534090471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10126585 | AAACTCCTCTTACTT[C/G]TGGAGAATTCAGCTG | 10277 |
rs534110362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10043487 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 10277 |
rs534129152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175338 | TAAAAAAGAAAAAAA[A/T]TTCAGCACCTACTTA | 10277 |
rs534152375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112099 | AATGGGATTCAGTCT[G/T]CACAGATCGGATGCA | 10277 |
rs534162443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074589 | GTGGTTGCTCTGAGT[C/G]ACTGTCTGGTCTGAC | 10277 |
rs534168580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104067 | GCCTGGCCTTACCTC[C/T]TCTTATGAAGTATAG | 10277 |
rs534179593 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154048 | GATCGCGCCATTGTA[A/C]TCCAGCCTGGGCAAC | 10277 |
rs534181834 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086803 | CAAGCAATTCTCGTG[C/T]CTCAGCCTCCCAAGT | 10277 |
rs534193771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065936 | TCAATTCAATTTTTT[A/T]AAAAATGGAAAATAC | 10277 |
rs534196759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161020 | CTGACTTGTGCCAGG[A/G]TAGCCAGGCTTTTAG | 10277 |
rs534205015 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047093 | ATTCTTCCATCCTAC[A/G]GTATCTGTGCCCATG | 10277 |
rs534209206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096893 | AAAATACAAAAATTA[C/G]CTGGGTGTGGTGTTG | 10277 |
rs534225079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10059655 | TAGGGCAAGGCCGAG[A/G]CGTGAAGGGCGGCAG | 10277 |
rs534243039 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144881 | TGAAATGAGCAAGAT[A/G]AATGGGTAAGATGGA | 10277 |
rs534273233 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134643 | AGTGGTGATGAGATA[C/T]ATGTCTTCTCATTGA | 10277 |
rs534296648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164942 | GATCTCTGTTTCCTG[A/C]CATTTAATGTCAGGG | 10277 |
rs534296865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107634 | CCAGGCCGGAGTGCA[A/G]TGGCGCAATCTCGGC | 10277 |
rs534300901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157037 | AAAAAAATTTTTGAG[A/T]CAGAGTCTTGCTTTG | 10277 |
rs534308963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142155 | TACTCAGAGCCTTGG[G/T]CTACCAGTGTTCCAT | 10277 |
rs534313605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062973 | AAAAAAAAAAAAAAG[A/G]AAAAGAAAATAGTGA | 10277 |
rs534325986 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110036 | TCAGCAAAGAAATAG[G/T]ACTTTATCCTTCCCC | 10277 |
rs534333762 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100608 | TGCCCAGGCTGGAGT[A/G]CAATGGTGCGATCTC | 10277 |
rs534353723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055414 | TGAACTCCTGGGCTC[C/T]GGTGATCCTCCTGTC | 10277 |
rs534464928 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10101787 | TGTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 10277 |
rs534488459 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10043741 | CCGGGATGCTTCTTA[C/T]AAATAGATGGTGTAA | 10277 |
rs534490606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118729 | GGCTGGTCTCTAACT[C/G]CCGACCTCATGTGAT | 10277 |
rs534508442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171444 | GGGTTGTTTTCCTTT[C/G]AGTGTGAAGAGCAGA | 10277 |
rs534512952 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10076669 | TTTCAGTTGCAAGTA[A/T]CTAAAGCAAGGATTG | 10277 |
rs534523795 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076108 | GAGTTTAAAAAGCTG[G/T]CATGAGGAAGGTGAT | 10277 |
rs534530677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111539 | CGTCGTTCTTCATCC[A/G]CCTGGTTCCGTGCAC | 10277 |
rs534539106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069455 | ACATGTCATAGGGCA[A/G]ATCAGAGCCACGGAG | 10277 |
rs534572877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10115564 | GGCTTGAGCCACCGC[A/G]TTTGGCCAATATCAT | 10277 |
rs534668310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151055 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10277 |
rs534724729 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10048550 | AGAAAAGGAGACTGA[G/T]AAGGAACAGCCACTG | 10277 |
rs534749788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10090958 | AGACATGAAATTTTT[A/G]TGTCCTTTGATGTTC | 10277 |
rs534764155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100981 | ATTAATAAGAAAAAA[C/G]ATGGACCATTATCAT | 10277 |
rs534781914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158883 | GGTGTGGTGGCGCAC[A/G]TCTGTTATCCTAGCT | 10277 |
rs534793696 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174009 | GGCACAGTGACACAC[A/G]GGGCTCCTTGAATGT | 10277 |
rs534823771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109277 | GAGCATCCTGAATCC[A/C]GACTCATGTTCACCA | 10277 |
rs534835440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077238 | TCTTCTGCCTTCCGA[C/T]AGTTGCTGGCAGTCC | 10277 |
rs534906269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086355 | TCAGGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 10277 |
rs534913324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10122403 | ACGGCATAAGGCATG[A/G]TATGCATTTGCCAGA | 10277 |
rs534929257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10177057 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 10277 |
rs534932729 | in-del | -/TTGT | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10128109 | AGTGGAATAATCTGA[-/TTGT]TTGAGTTCAGTGATG | 10277 |
rs534952552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114803 | CAGAAGGCGGAGTTT[C/G]CACTGAGCAGAGATC | 10277 |
rs534976933 | snp | A/G | 0.00016311 | 0.00902931 | intron-variant | UBE4B | GRCh38.p7 | 1:10178872 | GTTAACTGGAAATCG[A/G]TAACATTACAAGAGG | 10277 |
rs534999136 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10130958 | AAAGATAAACTATAA[A/G]TAAGTAGCCTGTGTC | 10277 |
rs535011889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079105 | ATTACAGGCATGGAG[A/T]TCTCCATTGTTTTCA | 10277 |
rs535027061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166037 | TCTGCCTTTCTTTCA[G/T]TAGGCTCATTCTTGA | 10277 |
rs535027388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173904 | GGCCTTTGTTTGGTG[A/G]CCAACCACACATTGC | 10277 |
rs535031192 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158083 | ATAATTCAGCTTTTG[G/T]TCATTGGTAAGTTGA | 10277 |
rs535047720 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138273 | CAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 10277 |
rs535050174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10071805 | CAAGTAGCTGAGACT[A/G]TAGGCAGGCACCGCT | 10277 |
rs535065403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158735 | TGTATAGGGCAGGGC[A/G]TGGTGGCTCACGCCT | 10277 |
rs535091560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151112 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 10277 |
rs535095430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10166880 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 10277 |
rs535119444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056655 | TCTTATAAATGGGGA[A/T]ATCGAGGCTCAGAGA | 10277 |
rs535129243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056945 | CAGCCTCCTGAGTAG[C/T]TGGGACTACAGGCAT | 10277 |
rs535129355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064868 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 10277 |
rs535216977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10145697 | CCTCGCCCCAACACT[C/T]ATCCAGTATATCTAG | 10277 |
rs535281435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042219 | GTGCATTTTCTCACA[C/T]GGCACTTGTAGTATC | 10277 |
rs535290702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070116 | GCCATGTCTACAAAA[A/C]ATTAAAAATTAGGTG | 10277 |
rs535331053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131587 | TAAAACTGTAACTGC[C/T]GGCTGGGCGTGTTGG | 10277 |
rs535334975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157742 | AGATCGTGCTACTGC[A/G]CTCCAGCCTGGCGAC | 10277 |
rs535335010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165770 | ATACCTTCCCTGACC[A/G]CCCTTTCCAGAATAG | 10277 |
rs535364388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10056041 | AGACCATACCATCCA[C/T]TTCTATCCCCTGGGA | 10277 |
rs535364834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177720 | CCACTTGTTTTGCGA[C/T]GGTGATACAAATACA | 10277 |
rs535388359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064180 | TGTTCCTCGTCTGCC[G/T]AACCCCTACCTGTCC | 10277 |
rs535389646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044481 | TGGTGGGAGGGGAAG[G/T]GATGGTTTTGAGATG | 10277 |
rs535397393 | in-del | -/AATAATGAC | 0.000803374 | 0.020026 | intron-variant | UBE4B | GRCh38.p7 | 1:10167474 | AATAATAATAATAAT[-/AATAATGAC]GACTAAGTAAAAGTT | 10277 |
rs535407017 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10109059 | CTAAATTCTCTCCCT[A/G]CTAGGAGGAATAAAA | 10277 |
rs535414144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116198 | CCCAGGCAGGAGTGC[A/G]GTGGCATGATCTCGG | 10277 |
rs535438895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10131885 | TTGAAACCGGGAGGC[A/G]GAGGTTGCACTGAGC | 10277 |
rs535446273 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10101786 | GTGTGGGATTACAGG[A/C]GTGAGCCACTGCGCC | 10277 |
rs535484275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151809 | AAAGTCAGATGATTG[G/T]CACCGAGACCCAGGG | 10277 |
rs535491422 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10167370 | CTTGAACCTGGGAGG[C/T]GGAGGTTCCGGTGAG | 10277 |
rs535494005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073687 | ATTGCGCTACTGCAC[C/T]CCAACCTGGTGATGG | 10277 |
rs535494816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145253 | ATATGGATAGATATG[C/T]TTCTGCTGTGATTAT | 10277 |
rs535500337 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | UBE4B | GRCh38.p7 | 1:10068046 | TTTTTTTTTTTTTTT[A/T]AAGATGGAGTCTTGC | 10277 |
rs535538038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10161364 | AGCTGCTTTGGGGCT[A/G]CATTTGTGGGTCTGA | 10277 |
rs535542802 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10065361 | AGCATGCGGGGGAGG[A/C]AGGCACAGCTCCACA | 10277 |
rs535546937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110035 | GTCAGCAAAGAAATA[G/T]TACTTTATCCTTCCC | 10277 |
rs535549499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042656 | TGTCTCAAAAGCAAA[C/G]AAACAAACAAACAAA | 10277 |
rs535568111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138405 | CCTGGCCCAATTTTT[G/T]GTATTTTTTGTAGAG | 10277 |
rs535577842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094283 | ACTAAGGTGTTCAAT[C/G]AATAAATGGATCGAT | 10277 |
rs535578914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10058792 | GTGTCACCTCAGGGC[A/G]GAAGACAGCAATGCC | 10277 |
rs535582041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049870 | CCCTCTAGTCTGGGC[A/G]AGAGAGCAAAAGACC | 10277 |
rs535583869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110942 | TAGAGGCTGCAGTGA[A/G]TCGTGATCATGCCAC | 10277 |
rs535592653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123502 | ATTAAAGAGGTAATG[A/G]GTAGTAATTAGAATA | 10277 |
rs535614352 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149982 | CATCTCTTTAAAAAA[A/T]AAATAAATAAATAGT | 10277 |
rs535630468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10043353 | AACTGTTTTTCAATC[A/G]TTTCTGAGATGTACT | 10277 |
rs535657224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094659 | CAGGATGGTCTCAAT[C/T]TCCTGACCTTGTGAT | 10277 |
rs535672438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178338 | GAAATGCGTGCTAGC[A/T]GTAAAAATTCAAAAA | 10277 |
rs535675575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070901 | GTTTTAGTGAATTAA[A/G]TTGGCTATTTATTCA | 10277 |
rs535676620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079255 | AGTCTGCCTCCCGGG[A/C]TCAAGTGATTTTCCT | 10277 |
rs535684391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10087599 | TTGCTCATGATAAGA[C/T]TGGGGTTGTGGGTTT | 10277 |
rs535721301 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094513 | ATCTTGGCTCACTGC[-/A]ACCTCCGCCTCCCGG | 10277 |
rs535750971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10074932 | ATTGACACATCCAGC[A/G]CTTTACCTGACATCT | 10277 |
rs535761879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036712 | AGACATTTCCAAAGC[C/T]TTTGCCTTTGTATTG | 10277 |
rs535823091 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105382 | TTAGGTTTTCCACTA[A/T]TATCCTTTTACCATT | 10277 |
rs535828420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120710 | GGGCATGGTGGCACG[C/T]ACCTGTAATCCCAAC | 10277 |
rs535858899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159495 | GGCTAACATGGTGAA[A/G]CCCCGTCTCTACTAA | 10277 |
rs535866978 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10064912 | GGGGTTACAGGTGCC[A/C/T]GCTGCCATGCCCAGC | 10277 |
rs535923156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160276 | ATTTTTCTTCCATGC[A/G]TCAGTCTTTGTGATA | 10277 |
rs535925205 | in-del | -/AAAAA | 0.00119856 | 0.0244508 | intron-variant | UBE4B | GRCh38.p7 | 1:10038281 | GTGAAACTCCATCTC[-/AAAAA]AAAAAAAAAAAGATT | 10277 |
rs535971016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106033 | TAAGTATAGCCTCTA[A/G]ATCAATAGGGCAATT | 10277 |
rs536000383 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084369 | TGCAAGGTGCTGTAT[A/C]ATCATGTTCCACCCT | 10277 |
rs536000623 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10035738 | TTTTTTTTATTTTTT[A/T]TTTATTTTATTTTAT | 10277 |
rs536011613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039011 | GTTGCAGTGAGCCGA[C/G]ATTGCGCCACTGTAC | 10277 |
rs536023757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086977 | GCGCCTGGCCTCCCC[A/G]TCTCTTTTTTAGTAC | 10277 |
rs536026488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10090234 | AGGTGACCCACCCCC[C/T]TCAGCTTCCTGAGTA | 10277 |
rs536062557 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051281 | ATGGAATACCATCTC[A/G]TAGCACTGTTCTTCA | 10277 |
rs536064904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083069 | TCGATGGGCATTTGG[G/T]TTGGTTCCATGTCTT | 10277 |
rs536065231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091131 | TGTGGAAGGTTTGTT[C/G]TATAGTTGATATGTG | 10277 |
rs536069847 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10065451 | TGTATTGTTGTCCAC[A/G]TATTCACCACCCCTG | 10277 |
rs536102046 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10083976 | ATCAATACACTTCCT[C/G]TTTTGACTTGGGGTT | 10277 |
rs536146261 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048183 | AACTAGCTTTTCTAC[A/C]ACAGGGATACCAGGA | 10277 |
rs536152064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132176 | CCCCCACTCCATATT[C/G]TGCTTTCATGCTCAT | 10277 |
rs536161776 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10128618 | AGCCACGTTTGTGAA[C/G]TCCTGCACTAGGCAG | 10277 |
rs536189482 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128164 | TTATCACCATATTAT[A/G]TAGATGTTCCTTCAT | 10277 |
rs536212828 | snp | C/G | 1.64974e-05 | 0.00287201 | intron-variant | UBE4B | GRCh38.p7 | 1:10129493 | TTTCAGTGAATATAT[C/G]ATAACCCAGAAGGCA | 10277 |
rs536249821 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10169924 | GGAAGCTGTGGCAGG[A/G]GAATCACTTGAACCC | 10277 |
rs536255023 | snp | C/T | 1.65877e-05 | 0.00287986 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171353 | GTTGAGTTGGTCTCT[C/T]TGTGAGTTTACTGGC | 10277 |
rs536260352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162421 | CTTGTGATCCGCCTT[C/T]CTCGGCCTCCCAAAG | 10277 |
rs536264959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10042400 | ACGCCTGTAATCCCA[A/G]CACTTTGGGATGCTG | 10277 |
rs536270050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176118 | GTAACCTTCTATGTC[G/T]GGCTTCCTTCACTTA | 10277 |
rs536277727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076466 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGT | 10277 |
rs536314369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155371 | CCTAAAGATAGTACT[A/G]TAAATACATCCACTT | 10277 |
rs536316580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10069248 | AATGATAATGATAAC[A/G]TCAACTAATAAATTA | 10277 |
rs536317495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061460 | CGGGGTTTCACCATC[A/T]TGACCAGACTAGTCT | 10277 |
rs536336110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034314 | ATTCTATCTTTTCCT[A/G]CTTCTTGAATCTTTC | 10277 |
rs536340485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137271 | TCAGGGGCAGGCAAT[C/T]CCATTGTGAACAGTA | 10277 |
rs536340744 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10121402 | ATAATACTTCTTTTT[A/T]ATTTTTATTTATTTA | 10277 |
rs536343138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10130148 | GCGCAATCTCAGCTC[A/G]CTGCAACCTCTGCCT | 10277 |
rs536373737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034889 | TCGGCGTTACTTTGT[G/T]TTTTTCGAATACAGC | 10277 |
rs536385263 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102806 | TAGGCTTACTTTTCC[C/T]CTAATCAGTGGGTGA | 10277 |
rs536400718 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180774 | TCAGGACTTATGTGA[C/T]TTATATTTTGGGGAG | 10277 |
rs536429180 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10098802 | AGCAACTCTCCTATT[C/G]AGTGGTGAGAAGTTA | 10277 |
rs536469041 | snp | A/T | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181625 | ACCAGCCTGGCCAGC[A/T]TGGTGAAACCCCATC | 10277 |
rs536484419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142446 | GAGGCCGAGGTGGGC[A/G]GATCACATGAGGTCA | 10277 |
rs536506276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10143074 | GATCGTGCCACTGCA[C/T]TCCAGGGCAACAGAG | 10277 |
rs536508011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075201 | ATATGTAAATGAGCA[A/T]GTGTAACTGTGTTCC | 10277 |
rs536532962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154825 | CCAGCCTGGGCTACA[A/G]GAGCAAATCTCCATC | 10277 |
rs536542655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127791 | GTCCCTCTCCTCAAG[A/G]CACTCATAATCTACT | 10277 |
rs536596870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10113975 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCTG | 10277 |
rs536600344 | snp | C/G | 3.40977e-05 | 0.00412888 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106513 | AGGCCCAGCAGCACG[C/G]GTCCACCCCTACCAC | 10277 |
rs536603953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041392 | CAGGCTTGAGTGCAA[C/T]GGCCTGATCTCGGCT | 10277 |
rs536620639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163286 | CTTGCTTCAGCAGCA[C/T]GTATACTAACATTGG | 10277 |
rs536635732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092942 | TGCCCCACTTGATCC[A/G]AAATGTGAAGATCAT | 10277 |
rs536638490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10069336 | AGAGAGTACCTACCA[C/T]GTGTCAGACACTGTT | 10277 |
rs536660948 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054899 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 10277 |
rs536662312 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090547 | GGTTGGCCATTACCT[C/T]TAAGACCAATGCCCC | 10277 |
rs536706717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10077319 | TCACATGGCCATCTT[C/T]GTTCTGTGTGTGTCT | 10277 |
rs536706744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086214 | CTGACCTCGTGATCT[A/G]TCTGCCTCGGCCTCC | 10277 |
rs536798542 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032301 | TCATCCATTTATACT[C/T]TCAAATTTTACCAAT | 10277 |
rs536807231 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155620 | TGATTAGGTCCTGGT[C/T]CCTGAGCAGATGGGA | 10277 |
rs536839719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175570 | GCAGGAGAATGGCGT[A/G]AACCTGGGAGGTGGA | 10277 |
rs536849029 | in-del | -/ATAGATAGATAG | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10126303 | AGACTCCGTCTCAAT[-/ATAGATAGATAG]ATAGATAGATAGATA | 10277 |
rs536888381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054728 | GGTAACACTTGCGGG[A/G]CATTTTTTTTGGAAC | 10277 |
rs536898571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076634 | CAGCAGTCATTTGGT[A/G]GCCCTCTTAGTTGGG | 10277 |
rs536924158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055333 | TTTCCTTTCTTTATT[C/G]TGAGACAAGATCTCA | 10277 |
rs536933060 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10107734 | AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTT | 10277 |
rs536970597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10048036 | AATTTTTATTAGAGA[C/T]GAGGGTCTCCCTGTG | 10277 |
rs536997523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122345 | AAATATGTAAGGCCC[C/T]GTTCCTGATTTCAAG | 10277 |
rs537090579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10164107 | GCACTTTGGGAGGCC[A/G]AGGCCGGCAGATCAC | 10277 |
rs537101524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078989 | GCCTGGCTAATTTTT[A/T]AATTTTTTTTGTAGA | 10277 |
rs537122963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10123656 | AGGTTATGAAATGAC[C/T]TCTGGGTGTTTTTTG | 10277 |
rs537123698 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10062930 | CATTGCACTCCAGCC[G/T]GGGAAACAAGAGTGA | 10277 |
rs537124304 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143007 | CCACTACTCAGGAGG[C/T]TGAGGTACGAGAATT | 10277 |
rs537140162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114640 | AGGCTGAGGCAGATG[A/G]ATCATTTGAGGTCAG | 10277 |
rs537147478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131486 | CAAGACTCCATCTCA[A/G]AAAAAAGAAACAGGC | 10277 |
rs537161674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124207 | CTCTCTGTTACCCAG[A/G]CTGGAGTGCAGTGGC | 10277 |
rs537162358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115732 | CATAGAGTATACTTA[C/T]ACAACCTAGATCATA | 10277 |
rs537176770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107571 | CTTTTTTTCTTTCTT[C/T]CTTTCTTTTTTTTTT | 10277 |
rs537195002 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162633 | TTTTTTTCTTTTTTA[A/G]TTTCAACTTTTATTT | 10277 |
rs537207855 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166799 | GCATGGTGGCACGCA[C/T]GTGTAATCCCAGCTA | 10277 |
rs537226904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092304 | ATCTTGGCTCACTGC[A/G]ACCTCCGCCTCCCAG | 10277 |
rs537247180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100902 | ATGACAACTTAGGAA[A/G]AATATTTCCAACATG | 10277 |
rs537273654 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10143840 | GGTCAGCCTGACAGC[A/C]CAGCCTCTGCCACAG | 10277 |
rs537274673 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10128543 | CCTTGTGATTTAATT[A/C]ACCAGGGGTGTGGCA | 10277 |
rs537279275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128692 | GCATCTCAACGTTGT[G/T]TCAATGCCTAAATGC | 10277 |
rs537343152 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032960 | GGGGTCACGTGATCC[C/T]TTTCAAAGATGGCCG | 10277 |
rs537346737 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164609 | TGAGCCAACTGAACA[A/C]ATAATATTGATTTTT | 10277 |
rs537357955 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177155 | TCATTGGATATATGA[C/T]TTGCAGATATTCTTG | 10277 |
rs537376561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058708 | GGAGAAGCACTTCAG[C/T]GGCTGGTGTGACACT | 10277 |
rs537386480 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10086058 | CTTACTGCAAGCTCC[A/G]CCTCCCTGGTTCACG | 10277 |
rs537391245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093727 | TGAGACGGAGTCTTG[C/G]TCTGTCACCCAGGCT | 10277 |
rs537405581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10034997 | TTTATGTGGGTTTTT[G/T]TTTGTTTGTTTGTTT | 10277 |
rs537445988 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10172836 | TGTCGATGCTGGACC[A/G]CAAAGACCATGTGGC | 10277 |
rs537509674 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173430 | GAGCTTGCAGTGAGC[G/T]GAGATCGAGCCACTG | 10277 |
rs537512140 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10175452 | GTCAGGAGATCGAGA[C/T]CGTCCTGGCTAACAC | 10277 |
rs537530937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10179348 | TTTCGCTGGTAGAAC[A/G]GGCTTTGTTTTCTTT | 10277 |
rs537540259 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176597 | CCTAGTGGGAGTGAC[A/G]TGGTATTTCATTGCG | 10277 |
rs537617525 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10103399 | AGAGCATTACCTCCT[A/C]TTTATTTATTTATTT | 10277 |
rs537647962 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041822 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGGTTAC | 10277 |
rs537654284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103942 | CATTTTTGTAGTTTT[A/C]GTAGAGACAGGATTT | 10277 |
rs537662333 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044085 | GCTCTGTTACTCACG[C/G]TGGAGTGCAGTGGCA | 10277 |
rs537669964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10150989 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10277 |
rs537710966 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174582 | TGGTGTGCGCCTGTA[A/G]TCCCAGCTACTCGGG | 10277 |
rs537712335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147418 | GAATCGTTTGAACCC[A/G]GGAGGCGGAGGTTGC | 10277 |
rs537725717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10041615 | GCTGGGATTACAAGC[A/G]TGAACGACTGTGCCC | 10277 |
rs537725800 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10048491 | CAAGAGGACTGAGCC[A/T]CCATCCATTCCAGCA | 10277 |
rs537762717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10042104 | CAGGCCCAGCCCTCC[A/G]GTGGACTTTCATTCC | 10277 |
rs537772410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10137357 | GCCACATCCATGTTG[C/T]TCAGTTGTCCAGAGT | 10277 |
rs537773253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10141121 | ATAATCCTACATAAC[C/T]GTCATGTTTCTGCAG | 10277 |
rs537791462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096684 | CCAAGATTGTGCCAC[C/T]GCACTCCAGCCTGGC | 10277 |
rs537832203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155160 | TGTTGCCTATAAGAC[C/G]AGTGCTGGGCCTAGT | 10277 |
rs537847254 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180484 | ATATATTCTGTGAGA[G/T]AACTGTGCCTGCTAC | 10277 |
rs537849739 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085794 | CCTGTATTCAGTGAC[-/T]TTTTTTTTTCTTTGA | 10277 |
rs537853576 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10081894 | TAATTTTTAAATTAT[G/T]TGTGCAGACAAGTTC | 10277 |
rs537889228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045649 | GGCATTCTGGCTGCT[A/G]TGAAGAGAATAGATA | 10277 |
rs537890476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074662 | AAACACGTTTTTCTT[C/T]TGGCTTCCAGAACAG | 10277 |
rs537892251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082707 | AGGTTTGTTACATAG[C/G]TACACATGTGCCATG | 10277 |
rs537912427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142522 | CTAAAAATACAAAAA[G/T]TAGCCGGTCATGGTA | 10277 |
rs537970880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039556 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 10277 |
rs537975335 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141404 | TGGGGTCATGAGCCA[A/T]TCCGGTAACCTCTGG | 10277 |
rs538024644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153326 | GCCTGGGCAACATGG[C/T]GAGACCCCATCTCTA | 10277 |
rs538046266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095835 | GGAGTGCAGTGGTGC[A/G]ATCATGGCTCACTGC | 10277 |
rs538087849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153929 | CTCTACTAAAAATAC[A/G]AAATTAGCCTGGCAT | 10277 |
rs538091176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161790 | TGGAAAGCACGTGCC[A/G]TGCCAGTACCAGTGC | 10277 |
rs538092794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10067018 | TTCACTTTTTTTTAA[A/C]GTAGAAAAGTAAGAC | 10277 |
rs538135606 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136551 | GGTAGGACAGAATAC[A/G]GTGGTCCTTGAATGG | 10277 |
rs538145891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112225 | ATGTAGTTATCAGAA[A/G]GTGGTTTGCATATTC | 10277 |
rs538150575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053076 | TCCTAATTTCATCAG[C/T]GACCCTCCCACCTCA | 10277 |
rs538151481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044421 | CCCAACCTTTTTGGC[A/G]CCAGGGACTGGTTTC | 10277 |
rs538158607 | in-del | -/TGGC | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10079785 | TTTGTTTCTTTTCTT[-/TGGC]TGCTAGTTTTTAACC | 10277 |
rs538159343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037554 | CAAGGTGGTGCTGTG[A/G]GTAGGTGGTGTGTTT | 10277 |
rs538180072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088485 | GGTTCAAGAAATTCT[C/T]CTGCCTCAGCCTCCT | 10277 |
rs538198864 | snp | A/T | | | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107224 | TTTGTTGTGGTAGTA[A/T]GTACGACAATCCTTT | 10277 |
rs538212158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127775 | AAGCTAGGAAGACAA[A/G]GTCCCTCTCCTCAAG | 10277 |
rs538213158 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031369 | GGCGTGAGCCACTGC[C/G]CCCAGCCCGGGAGTG | 10277 |
rs538223051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10148263 | AGCTCTGTTGTTTCC[A/G]TTTGAGTTGCACAAA | 10277 |
rs538273890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075117 | AGATAGTAAATATTT[C/T]TGGCTTTGGAGGCTG | 10277 |
rs538322790 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10128511 | AAAGGTGTTTCTGCC[G/T]GGCTCCCCACCCCAG | 10277 |
rs538344865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10119344 | GACATCAGTTTCTGC[A/G]GAGGCAGTACACTTG | 10277 |
rs538377198 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083878 | TATCTTACAGCATTA[C/T]TCCTAGGGTCATACT | 10277 |
rs538383772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120428 | CCTGGGAGGCTGAGG[C/T]CAGAGAATCGTTTGA | 10277 |
rs538412518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096740 | AAAAGAAAAAGGAGA[A/T]TTAAAAATATGAATA | 10277 |
rs538433428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066203 | TGCAGTGGTATAATC[A/G]TAGCTCGCTTCAGCC | 10277 |
rs538451198 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10097524 | GATATTATTTTAAAA[A/T]ATCAGGCCAGGAGCA | 10277 |
rs538451258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089141 | CCTCCCTAGTAGCTG[A/T]AACTGCAGGCATGTG | 10277 |
rs538456802 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079544 | ATATTTTTAAAGATT[A/G]TAATACAGTTATTTA | 10277 |
rs538528350 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171619 | AAACACGGTGGCTCA[C/T]GCCTGTAATCCCAAC | 10277 |
rs538531833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061317 | GGAGTGCAAGTGGCA[C/T]GATTTTGGCCCACTA | 10277 |
rs538558936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134504 | GCAACAAGAGTGGAA[C/T]TCCATCTCAAAAAAA | 10277 |
rs538560006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10113203 | GGCGAGAGCAGGAGC[A/G]ACAGAGAGGAGGAGG | 10277 |
rs538572307 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138137 | GAGTCTCACTCTGTA[A/G]TCCAGGCTGGAGTCC | 10277 |
rs538592907 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180548 | ATATTCACATATTTG[C/T]TTTTTTAATTGGTGT | 10277 |
rs538599278 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148454 | CTGGCCAACGTGGTG[A/C]AACACCGTCTCTACT | 10277 |
rs538610643 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049309 | TGGGGACACAGGAAC[C/G]CAACCAGCTAGACTT | 10277 |
rs538615321 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100376 | GGCTGGGATACAGTG[A/G/T]TTATTCACAGGCACA | 10277 |
rs538626761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175458 | AGATCGAGACCGTCC[C/T]GGCTAACACGGTGAA | 10277 |
rs538636899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065322 | AGCAGGATATAGAGC[A/G]GTTATGGGGCAAGTG | 10277 |
rs538657811 | in-del | -/C | 0.0158469 | 0.0875917 | intron-variant | UBE4B | GRCh38.p7 | 1:10082797 | TTGTCCTAATGCTCT[-/C]CCCTCCCCTTGACCC | 10277 |
rs538670564 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068467 | TGATTCTCCTGCCGC[A/G]GCCTCCTCAGTAGCT | 10277 |
rs538678095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10143055 | AGAGGTTGCAATGAG[C/T]TGAGATCGTGCCACT | 10277 |
rs538692149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161821 | TCTTTCCTGACGTGC[A/G]TAGCAGCCACTGAGA | 10277 |
rs538703708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169860 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGC | 10277 |
rs538716173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085094 | GAAGAATTTGTCACC[A/T]TTAACACCTAGAGTT | 10277 |
rs538746573 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116641 | TTTTAACTTTGTTTA[A/G]TGTCCTCAAATTTAA | 10277 |
rs538750086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10135967 | ATATTCCCAAAGTTG[A/G]AGGAAAAAGGAATAA | 10277 |
rs538760005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129613 | CATTTTTGTTAGACA[C/T]GTTATATCCTGCATT | 10277 |
rs538769987 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096245 | AGGTAAGCCAAATAA[A/G]TACCCTATTTGCTTC | 10277 |
rs538770955 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033037 | GTAGGGGTGGAGGGG[C/T]AGGAGGATTTACTCT | 10277 |
rs538784970 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10175646 | ACAGAGCGAGACTCC[A/G]TCTCAAATAAATAAA | 10277 |
rs538832507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113245 | TCTTTTAAACAACCA[G/T]ATCTCACGTGAACTC | 10277 |
rs538853702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141246 | TTTGCAGCTGTGATA[C/T]CAGGTTCATGATCTT | 10277 |
rs538860243 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093846 | ATTATAGGAGTGGGC[C/T]ACCACGCCCAGCTAA | 10277 |
rs538902357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148945 | ACTCCATCTCAGGGG[A/G]GAAAAAAAAGAAATC | 10277 |
rs538908377 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146760 | AGACCTGGTGGTACT[C/T]GGTGGTTTGCTTGCC | 10277 |
rs538917220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038198 | GGCAGGAGAATTGCT[G/T]GAACCCGGGAGGCGG | 10277 |
rs538921471 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045371 | CACTCAGGCAATGCA[A/C/G]CCTTAGGTCAGAGAC | 10277 |
rs538932816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053665 | ATGCTCTCCCTACCC[A/G]CTGCATGGCTGATTT | 10277 |
rs538969098 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122266 | ATGTGCCCATTTCAA[C/T]GAATCAGTCAAACAT | 10277 |
rs538971516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046554 | GGCTGAGCTGTGAGC[A/G]CTTCCTCCCCTGGCA | 10277 |
rs539003328 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114597 | GGCCAGGTGCTGTGG[C/T]TCACACCTGTAATCC | 10277 |
rs539019318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099897 | AATGGTGCTAGGGCA[A/G]TTGTTCAATCGGGGA | 10277 |
rs539044628 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102279 | GGAGGAAAATTGGTC[A/C]TGCACCTGGAGTGTT | 10277 |
rs539057691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092377 | CTACAGGTGCATGCC[A/G]CCACGCCCAGCTAAT | 10277 |
rs539066459 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117623 | GAAATGGATTAACTT[-/A]AAAAAAAAAAAGCCT | 10277 |
rs539067155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047132 | TAAGCCAATGCTGCA[C/T]ATTTGTATTGTTAAG | 10277 |
rs539070826 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084890 | TGTATTTTTAGTTGA[C/G]ACAGGGTTTCACCAT | 10277 |
rs539132192 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10043462 | ATGGAGTCTCACTCT[C/T]GTCACCCAGGCTGGA | 10277 |
rs539160972 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10139781 | TTGCCCAGGCAGGAG[G/T]GCAATGGTGCAATCT | 10277 |
rs539167035 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10036776 | GTAGGTGACATTGAT[G/T]TGATTACAAAATAAT | 10277 |
rs539173173 | snp | C/T | 0.000109828 | 0.00740958 | intron-variant | UBE4B | GRCh38.p7 | 1:10178615 | CCTGACGTACATTTA[C/T]GTCTCACATTGCCAT | 10277 |
rs539231541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068305 | AAAATGCTGGGATTA[C/T]GAGCATGAGCCACTG | 10277 |
rs539253874 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10063746 | AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA | 10277 |
rs539269207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061445 | ATTTTTTATTAGAGA[C/T]GGGGTTTCACCATCT | 10277 |
rs539326547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054605 | TTTAGAGCGCTTAAT[A/G]TGCTCAATATGCATA | 10277 |
rs539360527 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE4B | GRCh38.p7 | 1:10049593 | CTAAAAAAAAAAAAA[A/T]TTTTTTTAAATTAGG | 10277 |
rs539360560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145372 | GGAGGCCTAGGCGGG[C/T]GGATCACGAGGTCAG | 10277 |
rs539367551 | snp | A/T | 0.000151619 | 0.00870553 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106498 | AGCAGTTCCAGACAG[A/T]GGCCCAGCAGCACGG | 10277 |
rs539391372 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066925 | AAAAACCAAAACAGA[A/G]CTAGGAGTTATTGTC | 10277 |
rs539403409 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10102666 | TCCACTGGCCTCGGC[C/G]TTCCAGAATGCTGGG | 10277 |
rs539417485 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168840 | GAGCTGGCAGTGAGC[C/T]GAGATGGTGCCACTG | 10277 |
rs539465147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10047044 | GATATCACGGGTTTT[A/G]CCAAATGTTTTATTG | 10277 |
rs539492630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160955 | CTCAAAAAGAAACAA[A/G]ATTAACATAATCTAA | 10277 |
rs539504001 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164062 | AAACAGAGTCTTGAC[C/T]GGGCACAGTGGCTCA | 10277 |
rs539507989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139093 | GTATCAAGGTTATGC[A/T]GCCTTATAGAAGAAA | 10277 |
rs539520566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132251 | TCAGGCTCTTCTAAA[A/G]TGAGTAGAAGTGGGA | 10277 |
rs539521467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059579 | GCTTGAAGCCCATTG[A/C]GCTCATGCAGTTCCC | 10277 |
rs539556768 | in-del | -/TTTTC | 0.00241157 | 0.0346406 | intron-variant | UBE4B | GRCh38.p7 | 1:10055274 | CACCTTTTCATCATT[-/TTTTC]TTTTCTTTTCTTTTC | 10277 |
rs539570516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116226 | CGGATCACTGCAACA[A/G]CCTCCTCCCACGGTC | 10277 |
rs539576595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10103993 | TCTCGATCTCTTGAC[C/T]TCGTGATCTGCCTGC | 10277 |
rs539600622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165877 | TTCTATGAAGCAGAT[C/T]CTCCCTAACGGAATC | 10277 |
rs539603249 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10037378 | GTTGTTTGTTATTTA[G/T]ATAGTGTATTACAGT | 10277 |
rs539626049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088431 | TGTTGCCCAGGCTGG[C/T]GTGCAGTGGCGCAAT | 10277 |
rs539635467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10179191 | CAGGCTTTCTTCTCT[A/G]TTCCCTCCCCCCAGC | 10277 |
rs539636261 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108146 | TGGGATTTGGGGGAG[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs539647124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174532 | ATGGTGAAACCCTGT[A/T]TCTACTAAAAATACA | 10277 |
rs539662398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10158784 | GAGGCAGAGGCGGGC[A/G]GATCACTTGAGGTCA | 10277 |
rs539680812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064225 | AAGTCAAGTAGTAAG[C/G]ACATAGCATTTGTAT | 10277 |
rs539697805 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10073838 | TCTGCTGATCTGTTT[C/G]ATACCTTCTCGAGTG | 10277 |
rs539710395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109211 | CAGGGGGAACGGGGG[C/G]GCCGGGGGGACAGAC | 10277 |
rs539780952 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087072 | TACAGTGGAGTTTGC[C/T]CTGATTTCTCATTCT | 10277 |
rs539793767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111225 | TACTACACACACACA[C/T]ACCACGCGCTACACA | 10277 |
rs539794827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118665 | ATGAGCCACCATGCC[C/T]GGCTAATTTTGTATT | 10277 |
rs539801390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173749 | GAGCTGTTTAGTGTG[C/T]GCCCTCTCCAGGGTG | 10277 |
rs539805973 | snp | A/C/G | 3.30596e-05 | 0.00406558 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178718 | CAAATCCACAATAGC[A/C/G]ATAGAAAAATTTAAG | 10277 |
rs539830872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103470 | ATGGAATCTCACCCT[A/G]TCACCAGGCTGGAGT | 10277 |
rs539853712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10058895 | GAGTGGCACTATAAG[A/G]GTCTGACTGGCCTCA | 10277 |
rs539862119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166418 | AAAGCTTAGTAGTCC[A/C]CAGGCACTTGTAGAG | 10277 |
rs539869238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174152 | TGTAATCCCAGCACT[G/T]TGGGAGGCCAAGGTG | 10277 |
rs539879512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132284 | GGAGAGAACGTGGGA[A/C]GTAGGCTAGCTGTTC | 10277 |
rs539885217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153465 | GCTGCGTTCCAGCCT[A/G]TGAAACAAAGCAAGA | 10277 |
rs539894418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064588 | CTGTGTCTGCATCAT[C/T]ATCATTACCCTTCAG | 10277 |
rs539932729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125445 | CCATAGAATGATCTC[C/T]TCCAGAGCTGTATTG | 10277 |
rs539947682 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174987 | GTATGTCTTGTTTTC[C/T]GGGAAAGACAAAGGA | 10277 |
rs539953213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147469 | CTGCACTCCAGCCTG[A/G]GCGACAGAGCGAGAC | 10277 |
rs539958607 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083344 | CCAGTGATTGATGCA[A/T]GGCAGGGCTAGAGCA | 10277 |
rs539974370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10167064 | TTGAACCTGGGAGGC[A/G]GAGGTTACAGTGAGC | 10277 |
rs539999812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125286 | TTATGAACTAATTTT[C/T]GGTGATTCTGGAACC | 10277 |
rs540001391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080074 | CTTTCTCAGGCTCCC[A/G]GCTATGCATTGTAGA | 10277 |
rs540017820 | in-del | -/A | 0.0149889 | 0.0852631 | intron-variant | UBE4B | GRCh38.p7 | 1:10054072 | TATTAGATTTTTTTT[-/A]AAAAAAAAAGACAGG | 10277 |
rs540024504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102090 | TTATTGGAAGTTGCA[C/G]TGTAAACAAAAATAA | 10277 |
rs540037910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10152024 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 10277 |
rs540068382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074420 | AGGAACTCTCTTGAT[C/G]TAATTCCCCCTGCCA | 10277 |
rs540095039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138496 | GCCTCCGCCTCCCAA[A/G]GTGCTGAGATTACAG | 10277 |
rs540095678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049621 | AGGAAACAATGTTGG[C/T]TGGGCATAGTGTCTC | 10277 |
rs540113679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035401 | ACTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTGA | 10277 |
rs540136265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126026 | TGATAGAGGGCCAAG[C/T]GCGGTAGCTCATGCC | 10277 |
rs540152031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036038 | TGTGAGCCACCGCGC[A/C]CGGCCGAGGTAGTTT | 10277 |
rs540159517 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031562 | AAACTTTTAACATCA[A/G]TGTCACCAGGGGTTC | 10277 |
rs540177037 | in-del | -/CCTC | 0.00318978 | 0.0398085 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033604 | CCTTCCACTCTCCTT[-/CCTC]CCGCCGTGGTCTCGA | 10277 |
rs540210655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10079455 | GTGAGCCACCGCACC[C/T]GACCTCAAAATTTAC | 10277 |
rs540244711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072314 | GATTAAAATGAAGCA[C/G]ACATCAGCTCTTTAA | 10277 |
rs540403714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093915 | GGCCATGCTGGTCTC[C/G]AACTCCTGACCTCAA | 10277 |
rs540413491 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180106 | AGCAAACGCTGAGAC[C/G]TGAAAGGACATGGAT | 10277 |
rs540419027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10065052 | AAAGGTGTGAGCCAC[C/T]GCGCCTGGCCCTAAA | 10277 |
rs540420060 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037058 | GTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 10277 |
rs540425633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159601 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 10277 |
rs540438817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094495 | CTGGAGTGCAATGGC[A/G]CAATCTTGGCTCACT | 10277 |
rs540440630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086494 | GGGACTCAAAATCCC[A/G]TTATATGCATATATC | 10277 |
rs540494304 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040709 | TGCAACCTCTGCCTC[C/G]CAGGTTCAAGCGATT | 10277 |
rs540539553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153610 | GGATCACCTGAGGTC[A/G]GGAGTTCGAGACTAG | 10277 |
rs540582570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087119 | TACAGGTGTATCTAT[A/G]GAACTTGTAAACACG | 10277 |
rs540661619 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177643 | CCTGAGTGACAGAAT[A/G]AGACTCTGTCTCAAA | 10277 |
rs540677617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140647 | TTCAATGGAACCATC[C/T]AGAACCTTTGCTCCT | 10277 |
rs540681093 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076192 | GATTTATTATCCACC[A/G]AATGTGATTGAGAGA | 10277 |
rs540706597 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10037849 | GCATGAGCCACCATG[C/T]CCAGCCAAGTAGGTG | 10277 |
rs540734990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038211 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGGG | 10277 |
rs540750667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134093 | CATTTATTGTGTTTC[C/T]ACTTACTAATTTTGA | 10277 |
rs540765604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174908 | GAAGAGGTTGTAAAA[C/T]TGCATTTTCTTCTTT | 10277 |
rs540770920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10093090 | TTGTACACATACTAT[A/G]CTATACTACAGATAC | 10277 |
rs540772723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085520 | GTTTCTCTTTTGTTG[A/G]TAAGATTTGTCACTG | 10277 |
rs540787730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110403 | GAATTACCGTGTGTG[A/G]AAAGATAACTGTTGG | 10277 |
rs540801136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10055692 | TGGGAGGCCAAGGTG[A/G]GCAGATCACTTGAGA | 10277 |
rs540819861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068674 | TATTTTTAGTAGAGC[C/T]GGTGTTTCTCCATGT | 10277 |
rs540866170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162630 | TTTTTTTTTTCTTTT[A/T]TAATTTCAACTTTTA | 10277 |
rs540878589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10155530 | AGCTACTAAGGGACC[A/G]GTGTGAGGGTACCCC | 10277 |
rs540889055 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087670 | CACATCGTATCAGGG[G/T]TATATAATATCCACA | 10277 |
rs540895454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062351 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10277 |
rs540898234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146355 | CATTCGGGAGACTGA[A/G]GCAGGAGAATTGCTT | 10277 |
rs540903847 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051829 | GAATTGTACCCCTCC[A/C/T]AGCAGGGGGAGAAAA | 10277 |
rs540924525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111241 | ACCACGCGCTACACA[C/T]ACACCCCCACACCAA | 10277 |
rs540934023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053887 | AGACAAGGCCTCGCT[A/G]TGTTGCCCAGGCTGG | 10277 |
rs540965131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10036799 | AAAATAATACACTTA[C/T]ATTATTGAAACTTCA | 10277 |
rs540970692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046837 | ACCAGACTCTGAAAA[A/C]TTTGATTGTAGACCG | 10277 |
rs540990632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100108 | CATTCTCCCGCCTCG[A/G]CCTCCTGAGTAGCTG | 10277 |
rs541025854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108123 | GCTATTTAGTAACGG[A/G]AGAGGGGCTGGGATT | 10277 |
rs541062282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10047566 | GGCGTGATCTCGGCT[C/T]ACCGCAAGCTCCGCC | 10277 |
rs541062632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071127 | GGTCAGGCTGTTCTC[A/G]AACTCCTGACCTCGT | 10277 |
rs541066502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157415 | CCGAGAGGTTGAGGC[C/T]GCAGTGAGCCATTAT | 10277 |
rs541081949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144104 | TCTTCAAAATATGCA[A/G]CCTATTAGGTGATGG | 10277 |
rs541137389 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033448 | GGCTGCTCAGGGAAC[A/T]AGCGGCTGTAGTAGT | 10277 |
rs541137851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136871 | TTTGCAGTAAGCCAA[C/G]ATCGTGCCATTGCAC | 10277 |
rs541171526 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10092721 | TAATCCTAGCTACTC[A/G]GGAGGCTGAGGCAAG | 10277 |
rs541186159 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10113591 | AAGTGGCAGTGAGGG[G/T]TTCAAATTTAAGTTA | 10277 |
rs541209557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086073 | ACCTCCCTGGTTCAC[A/G]CCATTCTCCTGCTTC | 10277 |
rs541230841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163311 | CATTGGAACAATGCA[A/G]AGAAGATTACCATGG | 10277 |
rs541240301 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147397 | ACTCAGGAGGCTGAG[A/G]CATGAGAATCGTTTG | 10277 |
rs541242756 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052817 | GTGGGTGGCTTGTAC[A/G]CAGCAGCAATTTGTT | 10277 |
rs541304019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149497 | GGATTAACAGTGCAG[A/G]TAATGTATTCCTTGA | 10277 |
rs541308842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122625 | AATGCAGATATGTAG[C/T]GCTTAAAAATAAAGC | 10277 |
rs541322811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054984 | AGAGATGGGGTTTCT[A/C]CATGTTGGTCAGGCT | 10277 |
rs541355879 | snp | C/G/T | 3.29496e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161202 | CACGACGTTTTTGCT[C/G/T]GATGAAAGTCTGGAG | 10277 |
rs541359426 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162608 | CACCGCGCCCAGACT[-/T]TTTTTTTTTTTTTTT | 10277 |
rs541385472 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115562 | CAGGCTTGAGCCACC[A/G]CGTTTGGCCAATATC | 10277 |
rs541390184 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107560 | AGGAGAATTTTCTTT[C/T]TTTCTTTCTTTCTTT | 10277 |
rs541427351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158218 | TCTGTCGTGCCCTAC[A/G]TGCAAAAGAAGTGCA | 10277 |
rs541428650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063236 | CCGTGCCTCTGCACT[C/T]CCGCCTGGGTGATAG | 10277 |
rs541462965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093828 | ACCTCCCAAGTAGCT[A/G]GGATTATAGGAGTGG | 10277 |
rs541467069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063879 | TGCCATTGCACTTCA[C/G]CCTGGGCAACAAAAA | 10277 |
rs541511293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10108546 | TGCTCTTAAATTGAA[A/G]TTTCCTGTGGACTGA | 10277 |
rs541514285 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10135957 | TTTTCAGGTTATATT[C/G]CCAAAGTTGGAGGAA | 10277 |
rs541519263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048782 | AGAATGGGAGGAGAG[A/G]GGAGGGAGCTCAGGA | 10277 |
rs541536229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042267 | TGTAAACGGTTCATT[A/C]AACAGCGCTTACAGT | 10277 |
rs541562701 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10123010 | AAAATTCCAGTTAGT[G/T]TTGTGTATTCTGTCT | 10277 |
rs541574467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10176437 | TTTTCTACAGCTGCC[A/G]CCCATTTGACATTCC | 10277 |
rs541575836 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10111818 | AAAAATTAGCTAGGC[A/G]TGATGGCATGTGCCT | 10277 |
rs541607772 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104706 | AAGATTCTCTGTCTT[A/C]CACATGTAAGTGGCA | 10277 |
rs541632315 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10077426 | TTACGTCTGCTAAGA[C/G]CCTCCTTGCAAACAG | 10277 |
rs541647841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055076 | CAGGTGTGAGCCACC[A/G]CACCCGGCGTGTTTT | 10277 |
rs541665764 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033501 | GAAGCCAAGGCAGTT[G/T]AGTGCCTCTCGTGTT | 10277 |
rs541668053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172362 | CATTTAGTCCTCACA[A/G]AATCCTTTGAGGTAG | 10277 |
rs541668716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10070391 | TAAGTATACAACCCA[A/G]TGAGTTTTCATAAAG | 10277 |
rs541687318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055533 | ATGTTGCCCAAGCTG[C/G]TTTCCAACTCCTGGC | 10277 |
rs541700849 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166662 | GGCGCATTGGCTCAC[A/G]CCTGTAATCCCAGCT | 10277 |
rs541718600 | in-del | -/AAAAAG | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10144745 | TCTTAAAAAAAAAAA[-/AAAAAG]AAAGAAAGAAAGAAA | 10277 |
rs541722287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048295 | GTTATCATCTGGTTT[A/G]AACATATTATGAATA | 10277 |
rs541750556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100192 | AGACGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 10277 |
rs541756744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175615 | GAGATCGCGCCACTG[C/T]ACTCCAGCCTGGGCG | 10277 |
rs541760555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040847 | CGGGTCTCAAACTCT[C/T]GACCTTAGGTGATCT | 10277 |
rs541764311 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108121 | CTGCTATTTAGTAAC[A/G]GGAGAGGGGCTGGGA | 10277 |
rs541771523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101463 | TAATAGGAACTAATT[C/T]AGAGCAAATTAGAAT | 10277 |
rs541777262 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10109440 | TCACTCCTTAATTAC[A/C]AAATGCCATCCCAGT | 10277 |
rs541780640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10172920 | CTCACCATTGTGTTA[C/T]AACTGCCGACAGGAT | 10277 |
rs541785012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092709 | GGCGCATGCCTGTAA[A/T]CCTAGCTACTCGGGA | 10277 |
rs541830229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10164751 | TGCTCATCTCCCTGA[C/T]GTCTGAGCTTGGTGA | 10277 |
rs541846429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064364 | AAAGGTGATACTCTA[C/T]GCACAAGCAAACTGC | 10277 |
rs541907403 | snp | A/G | 0.000280031 | 0.0118295 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130513 | AGGTTGCTTCTTTGC[A/G]GTTGTGGTTGCCGAA | 10277 |
rs541914215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102156 | AGCCTCCTAGTGGTG[C/T]AGTGCTTTATTTTGT | 10277 |
rs541938421 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10086225 | ATCTATCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 10277 |
rs541949386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102850 | TTTTTAAAATATCAT[C/T]ACTAATAATGAATTA | 10277 |
rs541968628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131282 | AGGAGTTTGAGAACA[A/G]CCTGGCCAACATGAC | 10277 |
rs541982267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10156934 | AGTACTTTGGAAGGA[C/T]GATGTAGGAGGATCG | 10277 |
rs542001383 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10107130 | AAAGTTTTAGTGTAT[G/T]GTTTATTTAAAAGGA | 10277 |
rs542034395 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10070461 | AAAAAAAAAAAAAAA[A/C]CATTACCAGATCCCT | 10277 |
rs542077452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173580 | ATTTAGAAACAGAAA[A/G]CAAGTCATAGCCTGC | 10277 |
rs542120353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071850 | TACAGTTGTTAAAAA[C/T]TCAAGTGATAGAGCT | 10277 |
rs542131042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108671 | GTTCAGAAGAATCAT[C/T]AGAGAATACGTAAAG | 10277 |
rs542136295 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10107739 | CCCGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 10277 |
rs542137495 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100675 | TTCTGCTGCATCAGC[C/T]TGCCGAGTAGCTGGG | 10277 |
rs542169665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112460 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 10277 |
rs542171263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104507 | GATTTTAAATGGATG[C/T]GTGAATATCAAGGAG | 10277 |
rs542192290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166134 | CCAGAGGGCACTCAC[C/G]GGCCAGCTTCAGCTC | 10277 |
rs542217278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152109 | TAAAAATAGAAAAAA[A/T]AATTAAATTAGCCGG | 10277 |
rs542226644 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10110227 | TTTGGAAGTAGTTGG[A/G]ACATACATTTATATG | 10277 |
rs542260197 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179891 | CCTTTTTTTCTTTTC[C/T]CAGTGCCAGAACTGA | 10277 |
rs542264189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154797 | CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA | 10277 |
rs542270502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057086 | CAAAATGCTGGGATT[A/G]CAGGTGTGAGCCACC | 10277 |
rs542281916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145579 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 10277 |
rs542305780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105278 | CCTATATATACTTTA[C/T]CCAGTTTCCCCTGAC | 10277 |
rs542333253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148447 | GACCATCCTGGCCAA[C/T]GTGGTGAAACACCGT | 10277 |
rs542334822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094564 | TCAGCCTCCTGAGTA[C/G]CTGGGACTACAGGCG | 10277 |
rs542346182 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10050770 | ACTATGTTGCCATGT[A/T]GCCCAGGCTGGTTTC | 10277 |
rs542358094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045981 | GAAGTCTGGGTAGGA[G/T]GCCGGGGCTGGTATG | 10277 |
rs542370463 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173048 | TAAGTAAATTCTATG[A/C]TGTTTACACAGCAAC | 10277 |
rs542402201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173042 | TTTGTGTAAGTAAAT[C/T]CTATGATGTTTACAC | 10277 |
rs542417097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175412 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGCG | 10277 |
rs542488203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076861 | AAGCTATTCTCCTAC[C/T]TCAGCCTCCCGATTA | 10277 |
rs542499151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127102 | AAGTCCTAGACAGGA[A/G]TTAAATGCACTTATT | 10277 |
rs542509128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066319 | GATTGGGGGGGGAGG[A/G]GGTCTTGCCATGTTC | 10277 |
rs542537957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10119001 | GATTCCCCTGCCTCA[A/G]CCTCCTGAGTAGCTG | 10277 |
rs542551697 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045760 | GGTTAGTGGTTGAGA[C/G]GGGGAGAAAGGGTCA | 10277 |
rs542563360 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033165 | GCTTCCCTTACAGTG[C/G]TGGGCTCTGCCAGGA | 10277 |
rs542647723 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10129076 | TTTTTTGTAAAAAAC[-/AT]ATATAGATACAGTAC | 10277 |
rs542671663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10060766 | TGAGATTCTGGACAA[C/T]TTTTTTTTTTTTGGA | 10277 |
rs542697577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121162 | CTGAGGTTAGGAGTT[G/T]GGGACCAACATGGTG | 10277 |
rs542753959 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037594 | ATAGGGTCTGGCTCT[A/G]TCGCCCAGTCTGGAA | 10277 |
rs542793352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074273 | AGATCCCATCTCCCT[G/T]CAGTTACTCAGCCTT | 10277 |
rs542798672 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062981 | AAAAAAGAAAAAGAA[A/T]ATAGTGATGGCGAAT | 10277 |
rs542818327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10090779 | TTTACGGTGGAATTT[A/G]GAAGCCTATGCATTT | 10277 |
rs542818432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10098292 | ATCTACCATATTGCA[C/T]GTTAAAAAGAAAATC | 10277 |
rs542843388 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10087223 | GAGCATAGGTAAAAA[-/TATT]AAGTAAGAAGACTTA | 10277 |
rs542858356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10142600 | CGCTTGAACACGGGA[A/G]ACGGAGGTTGCAGTG | 10277 |
rs542862168 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10134807 | GAAGCTGAGGTGGGC[A/G]GATCACTTTAGGTCC | 10277 |
rs542865756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10168635 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 10277 |
rs542872418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10135492 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 10277 |
rs542880219 | in-del | -/A | 0.365853 | 0.221536 | intron-variant | UBE4B | GRCh38.p7 | 1:10070443 | TATCCAGTTAAAATT[-/A]AAAAAAAAAAAAAAA | 10277 |
rs542892969 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171488 | CGGTGGCTCAGGCCT[A/G]TAATCCCAACATTCT | 10277 |
rs542895929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039159 | GGAATCCAACAGTTA[C/T]AGAATAGTGCCAGGT | 10277 |
rs542927627 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032560 | GGCGGGCGCGCACAG[G/T]CCAGTGGGAGCGATG | 10277 |
rs542956136 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146295 | CGTCTCTACTAAAAA[C/T]ACAAAAATTAACTGG | 10277 |
rs542965210 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175658 | TCCGTCTCAAATAAA[A/T]AAATAAATAAATAAA | 10277 |
rs542986710 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060071 | TTCTATTCAGTCGTC[A/G]GGTCCCTGTGTGTGT | 10277 |
rs543026567 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171466 | AAGAGCAGATTTGGG[C/G/T]TGGGCGCGGTGGCTC | 10277 |
rs543029581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076149 | TATTTTCTGTGGTCC[C/T]GGAAGTTAGACATAG | 10277 |
rs543040850 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10129727 | GGGATCTTGGCACAC[G/T]GCAGCCTACGCCTCC | 10277 |
rs543049492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053400 | GTGATCCACCCGCCT[C/T]AGCCTCCCAAAGTCC | 10277 |
rs543087636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121684 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCATGCTT | 10277 |
rs543103465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099207 | AGATTGCACCACTGC[A/C]CTACAGCCTGGGTGA | 10277 |
rs543123032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113718 | ACATGCTGGCTGGGG[G/T]TGCTGCATCAGACTG | 10277 |
rs543149008 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068989 | TATGGACCTGCCTCT[C/G]TCTCTTAACTCTTTC | 10277 |
rs543159274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114122 | CCCAGAAATGTAAAG[A/C]TGTGAGAAGAATGGG | 10277 |
rs543167895 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10135571 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 10277 |
rs543182229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091805 | AAACAGGGTTTCACT[A/G]TGTTGGTCAGGCTGG | 10277 |
rs543188738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149035 | TTCATTTCTGGTTGT[A/G]GTTTCTTTGCCTACA | 10277 |
rs543192201 | in-del | -/GTG | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10085461 | GAGGGGAAAGCCTTT[-/GTG]AAGGGTCAGGAGATG | 10277 |
rs543200132 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181228 | TAAATGGTGACACAC[A/G]TTCAGAAGAAATCTT | 10277 |
rs543243703 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10169438 | CTTTTCCACTCTTTT[A/C]ACTTTCCACCTCATG | 10277 |
rs543244928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10083455 | TAGGAATGTCAACAA[A/G]ATCAAAGCCATTCTT | 10277 |
rs543273384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068551 | AGATGGGGTTTCCCC[A/G]TGTTAGTCGGGCTGG | 10277 |
rs543290465 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10119911 | GCAGAAAATTAGTAA[A/C]TGACTATACAGCAAC | 10277 |
rs543402659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10061752 | ACCAGCAAAGCTGAT[A/G]CTTGGATCTCTTCAT | 10277 |
rs543413421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114264 | AGGTACAAGCCTGTT[G/T]TAGCAAAGTTCATCC | 10277 |
rs543417099 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122417 | GATATGCATTTGCCA[G/T]ATAAGTAGTGTCAAA | 10277 |
rs543439926 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10163592 | ATAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 10277 |
rs543450085 | in-del | -/TTCT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047387 | GAGGGCTGCTCCAGC[-/TTCT]TTGAGGAAATCTGCA | 10277 |
rs543472634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10062607 | GTAAGCCGCTGTACC[A/G]GCCGCCTTAATGCAT | 10277 |
rs543474795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157221 | AGGCGGGGTTTTGCT[A/C]TGTTGGCCAGGCTGG | 10277 |
rs543482517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149384 | TCATGCCTGAAATTT[C/G]ATGTAACTGTTTTAA | 10277 |
rs543517800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046754 | TTGTAGGGCTAAACA[A/G]TTTCTCCAGCTTGCT | 10277 |
rs543520362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143326 | AGAATCGCTTCAACC[C/T]GGGAGTCAGAGGTTG | 10277 |
rs543550135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039879 | GTTGTTGCTGTATAG[A/G]AGCGAGGCAGTGGAG | 10277 |
rs543606578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10170029 | TAAATAAATAAATTT[A/G]TTTTAAGGCCTGCTC | 10277 |
rs543619899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10084550 | GATTGAAAGCTCTGA[A/G]AAAAAAAACTATCTT | 10277 |
rs543634165 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167319 | TGACACATGCCTGTA[G/T]TCCCAGCTACTCGGG | 10277 |
rs543706721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10130230 | CAGGCGCACACCACC[A/G]CGCCCGGCTAATTTT | 10277 |
rs543729765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10115598 | TGTATTCCAAGGTCA[A/G]TTATGTGTAGTTTTC | 10277 |
rs543730522 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162021 | TTTTTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 10277 |
rs543742562 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139171 | GAGGCCGAGGCAGAC[A/G]GATCACCTGAGGTCA | 10277 |
rs543747716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10079289 | TCAACCTCCTGAGTA[A/G]CTGGGATTACAGGCA | 10277 |
rs543808855 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139396 | CTGTCTCAACAAAAG[-/A]AAAAAAAAAAAGAAA | 10277 |
rs543809853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10159834 | ATAACTATTTGCCAG[A/G]TAGATTTCTGTGAAG | 10277 |
rs543819241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077375 | GCCACTGGATTAGGG[A/G]CCACCGTAATTGAGT | 10277 |
rs543829870 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101657 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAGC | 10277 |
rs543844449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10126097 | CGAGGTCAGGAGTTC[A/G]AAACCAGCGTGGCCA | 10277 |
rs543856909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063165 | CCCAGCCACTGGGGA[C/G]GCTGAGGCAGGAGGA | 10277 |
rs543868368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10167858 | CTTCGCAAAGTGCTG[A/G]GATTACACGCGTGAG | 10277 |
rs543930707 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10167268 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs543949812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118442 | TCCTAGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 10277 |
rs543963613 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10092582 | CCTGTAATCCTAACA[C/T]TTTGGGAGACTGAGG | 10277 |
rs543976548 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133043 | AGCTGCTATGTAGAC[A/G]GACCAAAACAGAAGG | 10277 |
rs543989255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138617 | ATGTCTATAAATGAT[A/G]ACAATTTTATTTCTT | 10277 |
rs544001181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085353 | CTCGTGGCCTCAGGC[C/T]TCTTGACTTCAGGCG | 10277 |
rs544003451 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10141634 | ATGTGCTTCTGTTGC[A/G]TCCAATTTTGTAATA | 10277 |
rs544008856 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143070 | CTGAGATCGTGCCAC[G/T]GCACTCCAGGGCAAC | 10277 |
rs544016019 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059230 | AGCGAGACTCCGTCT[C/T]AAAAACAACAGCAAC | 10277 |
rs544040686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094841 | TGTCACCTAGGCTGG[A/G]GTGCGGTGGTGTGAT | 10277 |
rs544051535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131975 | AAAACAACAAAAATG[C/T]AAAAACTAGCTGGGT | 10277 |
rs544061151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146124 | CTGTGCACCCCCCTA[A/G]GCAGTCCACAGATGT | 10277 |
rs544075044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040679 | CTGGAGTGCAATGGC[A/G]CGATCTCAGCTCGCT | 10277 |
rs544077317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087893 | TTCTATGAGGAAAAC[A/T]TGTCCCTTCTCCCCT | 10277 |
rs544078444 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033302 | ACCGCGCCACTATCA[C/G]GAAGAAACAGCAGGC | 10277 |
rs544123252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10133083 | GGAACAGACCCAAGG[A/G]GGCAGCCAGGAACAG | 10277 |
rs544155557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176360 | TTTGGGTCTACACTT[C/G]GGAGTGGGATTGTTG | 10277 |
rs544160201 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180225 | TAAAGCATGTCCTTC[A/G]TATGTCACAGTTTGG | 10277 |
rs544189340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10167127 | ACAGAGGAAGACTCC[A/G]TCTCAAAAAAAAATA | 10277 |
rs544193651 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146303 | CTAAAAATACAAAAA[C/T]TAACTGGGTGTGGTG | 10277 |
rs544202791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081281 | GTCAGGCTGGTCTCC[A/T]ACTCCCGATGTCAGA | 10277 |
rs544204308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073327 | TAAACCAGGATCTTG[A/G]TTAAATCCCATTCCC | 10277 |
rs544218196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065320 | GGAGCAGGATATAGA[A/G]CAGTTATGGGGCAAG | 10277 |
rs544221039 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180819 | TTTTTTTTAATGCTA[C/T]GTGACAGTTTGAAAC | 10277 |
rs544232527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117783 | GAGATCCCTGCCCTC[A/G]TGGAACTCACATTCT | 10277 |
rs544248612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10089324 | ACAAAATGTTTTTAT[C/T]AGGAAATTAGCTGCT | 10277 |
rs544285306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082270 | TTGGGAGGTCTAGGT[A/G]GGAGGATCGCTTGAA | 10277 |
rs544358196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087292 | AGTCCTAGTTTCTTT[A/G]TAAAATGAACATTTA | 10277 |
rs544363580 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031030 | CCACACGGTGTATTG[C/T]TCCACTGATGTGAAA | 10277 |
rs544375550 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10178072 | CATCAGTTCACCAGG[G/T]TGGTCTAACGTCCAT | 10277 |
rs544435775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036112 | TTTGATGATCTGTTA[A/T]TAGTCCTTGGTTTAG | 10277 |
rs544438667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051736 | CCAGGAGAAATGTTC[G/T]GCATATCAGGACTAA | 10277 |
rs544444847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154173 | TCTTGAACCCGGGAG[A/G]CAGAGGTTGCAATGA | 10277 |
rs544475718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052277 | GGGTCTCACTATGTT[A/G]CCCAGGCTGGTCTTG | 10277 |
rs544477368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10044242 | TATTTTTAGCGGAGA[C/T]GGGGTTTTACTCTTG | 10277 |
rs544478250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10059099 | GCCAGGTGTGGCGGT[A/G]GGCGCCTGTAGTCCC | 10277 |
rs544496891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125615 | TACTCCTATTACAAC[G/T]TGTTGGCATTCAGAT | 10277 |
rs544523572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174286 | GTAATTCCAGCTACT[C/T]GGAGGCTGAGGCAGG | 10277 |
rs544557023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080390 | CCACCACTGCACTCC[A/T]GTGTGGTGAGAGTGA | 10277 |
rs544565478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10118833 | TTATGTTTTTTTTAG[C/T]GGAGATGGGGTTTCA | 10277 |
rs544592500 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10141552 | TGAGGTTGTGGTAAC[A/T]TGTTACAGCAGCAAT | 10277 |
rs544595186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090378 | ACTCCACCTTGGCCT[C/G]CAAAAGTTCTGGAAT | 10277 |
rs544616514 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10175165 | CAGAGCTCCATGCCA[C/G]AGAAGTGGGATACCA | 10277 |
rs544672573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039087 | ACAAAAAAACACACA[A/C]ACAGAAAAACAAACA | 10277 |
rs544705874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127160 | AAGATAACTTATCTC[A/C]TAGCAATGAGCATAC | 10277 |
rs544715875 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070686 | AGATGCCCTGCTGTT[A/T]GTAGGAGTTCAACAA | 10277 |
rs544731898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083106 | TGTAAATAGTGCTAT[C/T]GTGTACATGTGTCTT | 10277 |
rs544742744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127833 | AGCTACAGCGCAACA[A/G]TTGAACAGATACTGT | 10277 |
rs544743688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154326 | GAGAAGCTGAGGCAG[A/G]AGAATAGCTTGAACC | 10277 |
rs544766501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043090 | TGTCAGCTCACTGCA[A/T]CCTCCGCCTCGGGGG | 10277 |
rs544768305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103745 | AAGCAATTCTCCAGC[C/T]TCAGCCTCCCGAGTT | 10277 |
rs544799746 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042634 | CCTGGGCGACAGAGT[A/G]AGACTGTGTCTCAAA | 10277 |
rs544814308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10104152 | CTGCTTTAAGTGCCT[A/G]TGAAGCCATGTATAG | 10277 |
rs544827430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059680 | CGGCAGCCGATCCCT[A/G]TCCTGACAACACCCT | 10277 |
rs544834359 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045182 | GTGATGGGGAGTGGC[A/T]GCAAATACAGATGGA | 10277 |
rs544887817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126307 | TCCGTCTCAATATAG[A/T]TAGATAGATAGATAG | 10277 |
rs544903386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133147 | TCGGTCCGGGTGAGA[C/G]AGGCCAGTGGCTGCA | 10277 |
rs544908892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104096 | AGATATAGTGGGTGG[C/T]CTCCAGGGATCCTGA | 10277 |
rs544950841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10111336 | TCATGTACTGGACTC[C/T]TGTTCTTTGCACGTA | 10277 |
rs544951820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096916 | TGGTGTTGCATGCCT[A/G]TAGTACCAGCTACTT | 10277 |
rs544955224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10065913 | GTACCCTTTTGCAAC[C/T]GGCTTTTTCAATTCA | 10277 |
rs544961714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175481 | ACGGTGAAACCCCAT[C/T]TCTACTAAAAATACA | 10277 |
rs545008241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059365 | TGTAAGAGTCTGAAG[G/T]ACACTATTGTCAGAG | 10277 |
rs545009187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168509 | TCCAAATGCCTTACT[A/G]CACTTTGTGCTTAGA | 10277 |
rs545014982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065677 | AGACGTTATGGAGCA[A/G]GGCTACACTTTCATC | 10277 |
rs545024862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175599 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 10277 |
rs545026227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169501 | ATGGAACACGAAACA[A/C]AACAGCTCAGACACT | 10277 |
rs545041863 | snp | C/G/T | 0.0170251 | 0.090679 | intron-variant | UBE4B | GRCh38.p7 | 1:10066310 | TTTTTGTGGGATTGG[C/G/T]GGGGGAGGGGGTCTT | 10277 |
rs545047091 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031702 | TTACATATCTAGTAG[C/T]CAGGTTCCTATTTTA | 10277 |
rs545078388 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095023 | ACCTCAGGTGGTCCA[C/T]CTGCCTTGGCCTCCC | 10277 |
rs545086550 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032441 | TTTCCTGGAGGAGGT[A/G]GAAGAGTGTGTGGCA | 10277 |
rs545087357 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037342 | GTCTTGTGCTTTTAA[A/G]TAGAGTACTTTAACT | 10277 |
rs545102490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128012 | TTTATGCCAGAGCTC[C/T]TTCCATTGTACATGT | 10277 |
rs545134468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10170198 | TTTGCAAACCTTTAA[A/G]GTTTGCATTTTCACC | 10277 |
rs545136515 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063623 | TAAAAGGTACATCTG[A/G]GCCGGGTGAGGTGGC | 10277 |
rs545183987 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091549 | TCCTGGGCTCAAGCA[A/G]TCCTTCCACCTCACC | 10277 |
rs545184049 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10055942 | AAAACAAAACAAAAC[A/C]AAACCAGAAGTAGAA | 10277 |
rs545237512 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10126356 | AGATAGATAGATAGA[A/T]AGGAGGAAATATTGG | 10277 |
rs545238491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148381 | TCACGTCTGTAATCC[A/C]AGTACTTTGGAAGGC | 10277 |
rs545247359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174759 | GTGTGGTGTGTGTGC[A/T]GATTGTTGGGTATTT | 10277 |
rs545268096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052390 | GGTGATTTAATTAGT[A/T]AGATTTTCTGACTAG | 10277 |
rs545269227 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10038649 | ACAGCTTTTGTATCA[A/T]CATCCTACGTAACAC | 10277 |
rs545279990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074175 | CCATCAGCCTCAGTC[A/G]TCACATCCATCTGCC | 10277 |
rs545307740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039143 | GTAGAGGAGATAGAT[A/G]GGAATCCAACAGTTA | 10277 |
rs545345054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10177207 | TACAGAAATACCCAA[A/G]GCTAGGTACTTTATG | 10277 |
rs545368501 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088214 | ATGTATGATTCTATG[C/T]ATGATTCTGCCTTTT | 10277 |
rs545409481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10173207 | CTGCTGGCCGAGCGC[A/G]GTGGCTCATGCCTGT | 10277 |
rs545441100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075881 | ACATAGCAAAACCCC[A/G]TCTCTACAAAAAATT | 10277 |
rs545463426 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129631 | TATATCCTGCATTAC[A/G]GTTGTTCATTTCTAT | 10277 |
rs545508445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138408 | GGCCCAATTTTTTGT[A/T]TTTTTTGTAGAGACG | 10277 |
rs545537364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071341 | AATCCTAGTACTCTG[A/G]GAGGCCAAGGTGGGA | 10277 |
rs545539754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121083 | AGAAACATATAATAC[A/G]GCCAGGCGTGGTGGC | 10277 |
rs545541551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077457 | GAGTATTATTTCTTT[A/G]TTTTTGATCTGCATC | 10277 |
rs545617930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053212 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCGCTGC | 10277 |
rs545622851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10079319 | ATGCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 10277 |
rs545631509 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10151158 | ACAGAGCGAGACTCT[C/G]TCTCAAAAAAAAAAA | 10277 |
rs545632814 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10108397 | GCAGAGGCTGAAACA[C/T]AGTTCCGGATGTTGC | 10277 |
rs545654742 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10045928 | GACATGAAGTGGCAG[C/G]TGCTTAAGCCAGATA | 10277 |
rs545662030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041858 | CATGCCACTACTGCC[C/T]GGCTAATTTTTGTAT | 10277 |
rs545704839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042360 | GAGAGGGATAAAAAA[C/G]AAGCATGGCCGGGCG | 10277 |
rs545760634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090674 | ATCCTCTTGCCTCGA[C/T]CGCCCAATCTGTTGG | 10277 |
rs545828470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035251 | ATGCACCCGCCTCAG[C/T]CTCCCAAAGTGCTGG | 10277 |
rs545874168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057957 | GAGAAGGAACAGCTG[C/G]ACTGTCGGATGTGGG | 10277 |
rs545874332 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125033 | TGGGAGGCTGAGGCA[A/G]GAGAATCTCTTGAAC | 10277 |
rs545885513 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165180 | CACTGTGTCCAAAAC[A/G]GAACCCTTGATGTTG | 10277 |
rs545888251 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10055491 | AGCTAATTTAAAAAA[A/T]TTTTTTTGTAGCGAT | 10277 |
rs545909020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050977 | ATCAGAGTTCTAATT[C/T]AGAGTCAGACATACT | 10277 |
rs545937991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10124275 | CGAGCGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 10277 |
rs545940414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096058 | TTACAGGTATGAGCC[A/G]CTGTGCGTGGCCCAC | 10277 |
rs545951311 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136806 | CGCCTGTAATCCCAG[C/T]TTACTAGGGAGGCTG | 10277 |
rs546015946 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141532 | ATTGTGTGGTTTGGA[G/T]CCACTGAGGTTGTGG | 10277 |
rs546029950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10093377 | TGAATCAAAAGTTTT[A/G]CTGTATTCTGTGAAC | 10277 |
rs546030485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144746 | CTTAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 10277 |
rs546081153 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | UBE4B | GRCh38.p7 | 1:10166976 | ACACACACACAAAAA[A/C]AAAAAATTAGCTGGG | 10277 |
rs546085536 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159746 | CTTTTGCAACCCATG[C/T]TAGATCTTTGATCAA | 10277 |
rs546124953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102296 | GCACCTGGAGTGTTA[A/G]CCTGGTCCTATGGAA | 10277 |
rs546138444 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059547 | TATTCCCATTGTCTA[G/T]GAATTGAACAGGAGG | 10277 |
rs546144422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159556 | TGGGCGCGGTGGCGG[A/G]CGCCTGTAGTCCCAG | 10277 |
rs546145104 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115825 | ACTGCATGTTAGTGT[A/G]CTGAACACTCTAGGC | 10277 |
rs546147450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093886 | TTTAACTAGAAACAG[C/G]GTTTCACCACATTGG | 10277 |
rs546175598 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052670 | AACAAGGTAGCCTGC[A/G]TATTCATTTGTCATG | 10277 |
rs546175607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10050021 | AATATGAGAACATTG[A/G]AGAAAAACTGAAGAT | 10277 |
rs546198907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10152950 | AGCTAGGACCCAGTC[C/T]TCTGTGGAAGGCCCT | 10277 |
rs546203099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064172 | CGCTCCTTTGTTCCT[C/T]GTCTGCCTAACCCCT | 10277 |
rs546213650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110183 | CTCTCCATCTGCTGG[C/G]CCAGTGGATTCGATG | 10277 |
rs546232516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139449 | TTTTTATGTTCCCTG[A/G]AAGAGTTTATTGTAT | 10277 |
rs546274495 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147019 | TGACGAGAGCTTCCT[A/G]AGAAGATGTCTGAAT | 10277 |
rs546283433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10142314 | TAGTTTCCTATGACT[A/G]CAACAACAAATTACC | 10277 |
rs546288816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043595 | CCAAGCCTGACTAAT[G/T]TTTTTTGTATTTTTA | 10277 |
rs546312027 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119313 | GTCACCTCAAACTTA[C/T]GCTTCTTTCTTCTCT | 10277 |
rs546324489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088001 | ACATTACTTATTTTA[C/G]AGGAATTATTCCAGC | 10277 |
rs546327254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044119 | TCTCAGCTCACTGCA[A/G]CCTCCACCTGCCAGG | 10277 |
rs546349866 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10036503 | TTAATTTAAAAAATC[-/T]TTTTTTTTTTTGTAG | 10277 |
rs546369275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166264 | GCAGTGCAGTACCTG[A/C]TTGTATCCATGAGTC | 10277 |
rs546373910 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137163 | TTCTGCCTAGTTGCC[A/G]TCGCTATATCCGCAG | 10277 |
rs546428882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034772 | AAATTCTCCTGGGAT[A/G]GGACACGCAGTGGTG | 10277 |
rs546432888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057206 | GTTTTATGCCTTTGG[G/T]CCTTAGTTCTCACCA | 10277 |
rs546475731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109497 | TACAGTGAACTGTGA[C/T]CATCCAGATTTTGGC | 10277 |
rs546486851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152123 | AAAATTAAATTAGCC[A/G]GGCATGGTTGCAGGT | 10277 |
rs546511712 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10148375 | GTGGCTCACGTCTGT[-/A]AATCCCAGTACTTTG | 10277 |
rs546537257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165023 | TAACCTGATGTCCCC[C/T]GGTGAACATCACTGC | 10277 |
rs546561012 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10177258 | AGCACAGTGGCTCAC[A/C/G]CCTGTAATCCCACCA | 10277 |
rs546583326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10123919 | GCTGGGATTACAGGC[A/G]CCTGCCACCACACCC | 10277 |
rs546589288 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096133 | AGTTAAAAAAAATCT[A/G]TTGTTCTCATTTTGT | 10277 |
rs546597586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171461 | GTGTGAAGAGCAGAT[G/T]TGGGCTGGGCGCGGT | 10277 |
rs546600864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10080646 | CAAATAGCCAAGATA[C/T]GGAAGCAACCTAAAT | 10277 |
rs546626182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078583 | CTCGGGTTATTTTAT[C/T]TTACAGCCTTGTTTT | 10277 |
rs546692120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101726 | TGTTAGCCAGGATGG[C/T]CTTGATCTATTGACC | 10277 |
rs546697200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108972 | CTTTCTCTAACAACC[A/G]TATCAGATTGTGTGC | 10277 |
rs546707986 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131699 | AAACCTCGTCACTGC[C/T]AAAAATACAAAAATT | 10277 |
rs546715611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10124250 | CACTGCAACTTCCAC[C/T]TTCTGGGTTCGAGCG | 10277 |
rs546728113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093718 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 10277 |
rs546744317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10176787 | TTTTTTCTTTTTCTT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs546782472 | snp | C/G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143642 | TTCCCTCGAAGGATT[C/G/T]GGATGCGACAAGTTT | 10277 |
rs546785282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077813 | TAAAATATTTCAAAT[A/G]TACATGATAACATAA | 10277 |
rs546789076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086193 | AGCCAGGATGGTCTC[G/T]ATCTCCTGACCTCGT | 10277 |
rs546830320 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168765 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 10277 |
rs546877813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152207 | GAAGTTGCAGTGAGC[C/T]GAGATCCCGCCACTG | 10277 |
rs546890853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175608 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 10277 |
rs546904455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050078 | TTGCTGATCTGAAAG[A/G]CTGGTTTTTTTTGAG | 10277 |
rs546916946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087554 | TCATTACTTTGTAGA[A/G]TGTCCCTTAATTTGG | 10277 |
rs546919239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139224 | AACATAGTGAAAACC[C/T]GTCTCTACTACAAAA | 10277 |
rs546940963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043336 | AAACTTACTGAGATC[G/T]CAACTGTTTTTCAAT | 10277 |
rs546942144 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10155837 | AGACCAGCCTGGCCA[A/G]CATGGCGAAACCCTG | 10277 |
rs546957232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132023 | TAATCCCAACTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs546963524 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064220 | AACTTAAGTCAAGTA[A/G]TAAGCACATAGCATT | 10277 |
rs546964069 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10091976 | CTGGTCTCAAACTCC[G/T]GGCCTCAAGTGATCC | 10277 |
rs546967922 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094648 | ACCATGTTAGCCAGG[A/C]TGGTCTCAATCTCCT | 10277 |
rs546999870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139581 | TAAGACAGTTAATAT[A/G]TATAAGACTATTTAG | 10277 |
rs547000890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084678 | CTTTAGTTTTCCTTT[C/T]TTTCTTTCTTTCTTT | 10277 |
rs547023380 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141297 | GATTATGTGGGTAGG[A/T]CCAGTGTCATTGCAA | 10277 |
rs547041104 | in-del | -/AAAAAGAAAAAG | 0.00320255 | 0.0398876 | intron-variant | UBE4B | GRCh38.p7 | 1:10125128 | GAAATTGTGTCTGGA[-/AAAAAGAAAAAG]AAAAAGAAAAAGATT | 10277 |
rs547088265 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10075597 | GGTACCTCTATGCTA[A/C]GTAGTCCTGATTATG | 10277 |
rs547123554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094190 | CTGTGAGAAATCATC[A/T]GTCCCTGTACTAGTG | 10277 |
rs547150980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10097637 | CAACATGTTGAAACC[A/C]CGTATCTACTAAAAA | 10277 |
rs547226470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145686 | TGTCTCCCACCCCTC[G/T]CCCCAACACTCATCC | 10277 |
rs547288993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098777 | TAAAGGGCATCTACC[A/C]AAAAACTACAGCAAC | 10277 |
rs547297567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098842 | TCTGTAAAATCAGCA[A/G]TAAGAACAAGGATGA | 10277 |
rs547307403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045430 | GGGCTATGAGAGCCT[A/G]GTGTAACTGATGACA | 10277 |
rs547314305 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10178284 | CAAGGACTGAAATAG[A/T]CTAGATTTCCTTCTC | 10277 |
rs547386438 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175512 | AAAAATTAGCCAGGC[A/G/T]TGGTGGCGGGCGCCC | 10277 |
rs547395243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10143703 | ATGTTTCAGTTGTAG[A/G]CGAAAGAATCCAATT | 10277 |
rs547414332 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10135593 | AATACAAAAATTAGC[A/G]GGTGTGGTGGCACGC | 10277 |
rs547419580 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081896 | ATTTTTAAATTATTT[C/G]TGCAGACAAGTTCTC | 10277 |
rs547426509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129274 | TTTCAGAGGGAATGC[A/C]TGTGTGCCATTTTAG | 10277 |
rs547454226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041246 | GTAGAACCTGGACTC[A/T]AATCCAGGTTCTGAC | 10277 |
rs547455841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040074 | ATAGATAAGGGTTGA[A/G]TAAGGAATTCCAGAG | 10277 |
rs547455938 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032183 | GTGAGCCACCGCGCC[C/G]GGCCAAATATTTGTA | 10277 |
rs547482236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10150943 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 10277 |
rs547486732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10033985 | TTCTTCAGGGTATGC[A/G]AACAAGAAGGGCGAG | 10277 |
rs547492065 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032810 | CCCTTTGCCCCTCCC[A/C]ACGTCCGGCGCGGCT | 10277 |
rs547561408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171038 | GGATTCTTTGAAGAT[A/T]AATCCAACCAATTCC | 10277 |
rs547567962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10155045 | TAGTCAGTGTTCTGG[A/G]CCTGTCACTGTGGCT | 10277 |
rs547570806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100786 | CTCGAACTCCTGACC[G/T]CAGGTGATCCACCTG | 10277 |
rs547580794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041957 | ACCTCAGCCTCCCAA[A/G]GTTGTGGGATTACAG | 10277 |
rs547605958 | in-del | -/TTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067728 | CTCCCATCTCAGTAT[-/TTG]TTGTTGTTGTTGTTG | 10277 |
rs547608905 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10148175 | GAGCTTCCGGTGAGC[C/G]GAGATCACGTCTCTG | 10277 |
rs547629066 | snp | C/T | 1.67239e-05 | 0.00289166 | intron-variant | UBE4B | GRCh38.p7 | 1:10121945 | CATCACCGTCCCTAA[C/T]GTTCATGGGTCCACA | 10277 |
rs547651822 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079070 | GCGATCTTCCTGCCT[C/T]AATCTCTCAAAGTAT | 10277 |
rs547667372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114453 | TTTCTGTTTGTTCTA[C/G]TGTGTGTTTTTCCTG | 10277 |
rs547691948 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116896 | TTTACTATACTACTT[C/T]ACCTTTTTCACTGAT | 10277 |
rs547692767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155979 | AGGTCGCAGTGAGCC[A/G]AGATCTTGCCACTGT | 10277 |
rs547714270 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046841 | GACTCTGAAAACTTT[A/G]ATTGTAGACCGCGGA | 10277 |
rs547715457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039369 | GTGGGTTTTACCTCG[A/G]GTGTGTGGCAGGTAC | 10277 |
rs547751822 | snp | C/T | 0.000138785 | 0.00832907 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106525 | ACGGGTCCACCCCTA[C/T]CACCCGCCTCACCCA | 10277 |
rs547799818 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10047963 | GTTCAAGTGATCCTT[A/C]TGCCTTAGTCTCCTG | 10277 |
rs547804274 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10055274 | CACCTTTTCATCATT[A/T]TTTCTTTTCTTTTCT | 10277 |
rs547855805 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053948 | TGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 10277 |
rs547918654 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033529 | GTTCTTATTTTTTAA[C/T]CTCTGACTATGCAAT | 10277 |
rs547945112 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086976 | CGCGCCTGGCCTCCC[C/T]GTCTCTTTTTTAGTA | 10277 |
rs547947599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085885 | ACGTCTGCCTCCTGG[A/G]TTCAAGCAATTCTCC | 10277 |
rs547947665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093608 | TACTGTCATAGAATG[C/G]TGGAAGGGTTAAAAT | 10277 |
rs547955303 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133436 | TGGTACACAGTGATC[A/T]CTCAACCAATATTAA | 10277 |
rs547958729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10067989 | CACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 10277 |
rs547968351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163235 | CACGCTTGGCTAATT[A/T]AAAAAATTTTTTTTA | 10277 |
rs547971385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054195 | TATCTTCAAACCAAT[A/G]CAAATATTTTGTAAG | 10277 |
rs548009672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10046897 | TTTCATCTTTGCATG[C/T]GAATTGGCAAGCTTT | 10277 |
rs548022453 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089484 | ACCGCAGCCCAGGTA[G/T]CACTGAGAACATGTC | 10277 |
rs548024713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062106 | GTAGAGACGGTGTTT[C/G]ACCATGTTGGCCAGG | 10277 |
rs548030991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091156 | TATGTGGGGAGTTTA[A/T]TCATCTTCTAAAAGA | 10277 |
rs548034658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163678 | GTCTCAAATAAATAA[A/T]TAAATATTAAAGAGA | 10277 |
rs548045315 | in-del | -/AAAAG/G | 0.0178429 | 0.0930183 | intron-variant | UBE4B | GRCh38.p7 | 1:10134516 | AACTCCATCTCAAAA[-/AAAAG/G]AAAAGAAAAGAAAAG | 10277 |
rs548064618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062695 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs548080315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046324 | CAAACCCTTCTCCCG[A/T]GGGAGACAACCCCGG | 10277 |
rs548084650 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062234 | ACCATCATTTTGCTT[A/G]TGTCCTAATTTCCTT | 10277 |
rs548105030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084822 | ACTGCCTTAGCCTCC[C/T]GAGTAGCTGGGATTA | 10277 |
rs548112515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10039523 | CAGCCTCTGGTTCCC[A/G]GGTTCAAGTGATTCT | 10277 |
rs548145222 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044120 | CTCAGCTCACTGCAA[C/T]CTCCACCTGCCAGGT | 10277 |
rs548167168 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041275 | ACTCCAGAGTTTTCT[A/G]TCGCTTTACTACCTC | 10277 |
rs548229238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138095 | GTGCACCACCACGCC[C/T]GGCCAATTTTTTTTT | 10277 |
rs548229722 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043314 | GCACCCGGCCAACTT[C/T]CAGTAAAAACTTACT | 10277 |
rs548232792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122186 | AACATCCATGTGTTA[C/T]TAGAGAGAAGGCCTA | 10277 |
rs548253024 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102065 | ATCCTTTAGCAACAC[A/G]TGTTAATGATTATTG | 10277 |
rs548255928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129953 | CACCGCACCGGGCCT[G/T]TTTTTTTTCCCTTGA | 10277 |
rs548304617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069833 | TGTACAGATGTGCAG[C/T]GTACGGATGTCCATT | 10277 |
rs548320943 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099572 | TCTAAGAGTGAAAAA[A/C]ATTTTGGTCAAAATC | 10277 |
rs548332750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144824 | TACTCTGATTTTAAA[G/T]ATGTTACAATGCGAA | 10277 |
rs548336077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163856 | GGCTCAATTTATGCC[G/T]GCTGGGATTACAGGC | 10277 |
rs548362369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149586 | CAGTTTATAAATGTC[C/T]GAATGAACATCCCAA | 10277 |
rs548365300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042506 | ACAAAAATTAGCCGG[G/T]CGTGGTGGTGCACGC | 10277 |
rs548375437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142864 | GTGTATCGCAGCACT[C/T]TGGGAGGCTGAGGTG | 10277 |
rs548381290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142464 | TCACATGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 10277 |
rs548386245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093972 | AGTGCTGAGATTACA[G/T]GCGTGAGCCATCGTG | 10277 |
rs548402468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035465 | GCAGTGGCGCTATCT[C/T]AGCTCACTGCAAGCT | 10277 |
rs548413565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10107433 | TTAGGAACTAACTTC[C/T]ATAAGCTCTAACAAG | 10277 |
rs548423135 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | UBE4B | GRCh38.p7 | 1:10086846 | AGGCATGTGCCACCA[A/C/T]GCCCGGCTAATTTTT | 10277 |
rs548430893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040311 | GACGGTGTTTCACCA[C/T]ATTGGCCAGGCTGGT | 10277 |
rs548449368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108175 | TGTGTGTGCGTGCGT[G/T]CTCCCTTCCCACCCC | 10277 |
rs548449640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100365 | TATGCTGCCCAGGCT[A/G]GGATACAGTGGTTAT | 10277 |
rs548476944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10135693 | GTGAGCCATGATCAC[A/G]GCACTGCACTCCAGC | 10277 |
rs548498896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150643 | AAGGTGGGCAAATCA[A/C]GAGGTCAAAAGATCA | 10277 |
rs548500799 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042111 | AGCCCTCCAGTGGAC[A/T]TTCATTCCCGTTTGT | 10277 |
rs548508367 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032865 | CGGGGAGAGGACGCA[C/G]GCGAGAGGAACTCGG | 10277 |
rs548539537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115361 | CAGCCTCTGCCTCCC[A/G]GGATTTAAGAGATTC | 10277 |
rs548541028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144363 | AATGTACTTTCTTGC[A/G]ACAAAAAAGATGATT | 10277 |
rs548571783 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10118592 | TCACCGCAACCTCTG[C/T]CTCCTGGGTTCAAGT | 10277 |
rs548577040 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109841 | TTTTTAGCAGAGACA[A/G]GATTTCACCATGTTG | 10277 |
rs548581732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141016 | GGTCTCTGGTAGGTA[G/T]AATCATGTCAGTGAT | 10277 |
rs548598851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042035 | TGACTCCTGAATTCA[A/G]GCGATTCTCCTGGGT | 10277 |
rs548599377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048471 | GTGAGCATAAATGCG[G/T]AAGACAAGAGGACTG | 10277 |
rs548632715 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100191 | GAGACGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10277 |
rs548635584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034896 | TACTTTGTTTTTTTC[G/T]AATACAGCAGAAATG | 10277 |
rs548638050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048926 | TCCCATTCTCTGCTA[A/T]AATCACTACTTTCTT | 10277 |
rs548651703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096508 | AGGCCGAGGCAGGTG[G/T]ATCACTTGAGGTCAG | 10277 |
rs548655603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10086223 | TGATCTATCTGCCTC[A/G]GCCTCCCAAAGTGCT | 10277 |
rs548679128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176912 | TGCCTCAGCCTCCCA[A/G]ATAGCTGGGACTACA | 10277 |
rs548699078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147307 | AGACCAGCCTGGCCA[A/T]CATGGCGAAACCGTG | 10277 |
rs548705272 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10057905 | GTGGCAGGGAAGCAA[A/G]CATGGGAGGCAGTGG | 10277 |
rs548707778 | snp | A/G | 5.24315e-05 | 0.00511986 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106531 | CCACCCCTACCACCC[A/G]CCTCACCCAGTGCCA | 10277 |
rs548729192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078044 | AGACGGAGTCTCTCT[C/T]TGTCACCCAATCTGG | 10277 |
rs548730092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044360 | GCGCCTGGCCCAGTT[C/G]CATATTTAATTGCCA | 10277 |
rs548741158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10177445 | CAGTGAGCCGAGAGC[A/G]TGCCTCTGCACTCCA | 10277 |
rs548748173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062843 | TGCCTGTAATCCCAG[C/T]GACTCGGGAGGCTGA | 10277 |
rs548771374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038030 | CCACGCCTGTAATCC[C/T]AGCGCTTTGGGAGGC | 10277 |
rs548805227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157634 | AATACAAAAATTAGC[A/T]GGGCGTGGTGGCGCA | 10277 |
rs548806644 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10118512 | CCAGCTAATTTTTTT[G/T]TTTTCTTTTGAGACG | 10277 |
rs548807054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110923 | CTTGTCTGAGCCCAC[A/G]AGTTAGAGGCTGCAG | 10277 |
rs548825598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10055364 | CTGTTTCCCAGGCTG[A/G]AGTGCACTGGCAGCA | 10277 |
rs548847437 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10111379 | GCCTTAGGCCTTTGT[A/T]CTTGTTTCTCCCCTT | 10277 |
rs548862411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055824 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 10277 |
rs548881684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065353 | GCGGGAGGAGCATGC[A/G]GGGGAGGAAGGCACA | 10277 |
rs548885243 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179001 | TTGAGAGGAAGAAAC[A/T]TCCTTAGCTTAGCCT | 10277 |
rs548956730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162164 | CCACCACACCTGGCT[A/G]GTTTTTGTATTTTGT | 10277 |
rs548968803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155153 | CTGGGCCTGTTGCCT[A/G]TAAGACGAGTGCTGG | 10277 |
rs548972179 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123981 | GGTTTCACCATGTTG[C/G]CCAGACTGGTGTTGA | 10277 |
rs548989321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061159 | TTACTTGTAGAATTT[A/G]TAGTACTGGAATCCA | 10277 |
rs549025009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10103905 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGTGCC | 10277 |
rs549026615 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10045021 | GGGTGATGGGAGAAA[C/G]TGACAGATCATCAGG | 10277 |
rs549027849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053527 | TGGCACAATCAAGTT[C/T]TGGGGTATATGGGCT | 10277 |
rs549044650 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035033 | AGACGGAGTCTTGCT[C/T]TGTCGCCCAGGCTGC | 10277 |
rs549045105 | snp | C/T | 0.000115822 | 0.00760905 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180000 | CACAGCCAAGGCCAA[C/T]GAGGCAAGCAGAAGC | 10277 |
rs549061685 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170755 | ATACTGGCTGGAAGA[A/G]CTGACTCAAAACTTT | 10277 |
rs549087068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089013 | CACAAGAACAAAATG[G/T]TTTCTTTTTTTGAGA | 10277 |
rs549096995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10145672 | CCCTCCTCACCTGCT[A/G]TCTCCCACCCCTCGC | 10277 |
rs549099610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155811 | GTGAATCACTTGAGG[C/T]CAGGAGTTTGAGACC | 10277 |
rs549109459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147955 | TGTGTAGGCCGGGTG[C/T]GGTGGCTCACGCCTA | 10277 |
rs549109496 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121286 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 10277 |
rs549127565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10081835 | CTCAGGTGGGCTGCC[C/T]GCTTCGGCCTCCCAA | 10277 |
rs549127576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090108 | TATGTTAGGAATCAG[A/G]CAGCCTGTGTGTGTG | 10277 |
rs549144161 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180385 | TTTTTCCCCTCTCCC[C/G]CTTCCTGACCCTACT | 10277 |
rs549158385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168075 | CAGTTATGTGCTTGG[C/T]GCTTTGCTGAGCTGA | 10277 |
rs549173800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148759 | AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTCT | 10277 |
rs549182570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153263 | ATAATCCTAGCACTT[C/T]AGGAGGCCAAGGTGG | 10277 |
rs549209759 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031244 | ACAGGTGCCCGCCAC[A/C]ACGCCCTTCTAATTT | 10277 |
rs549241457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103315 | GATTTCTATAATACT[A/G]TGTAAATAGGTTAAT | 10277 |
rs549312783 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074993 | CTAGCATGCCCCAAA[A/C/T]CAAGCTTTGCTGTTG | 10277 |
rs549320075 | in-del | -/TGA | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10050943 | GTTAAGGTAGGCACT[-/TGA]TGAAAAAAGCCTCAT | 10277 |
rs549339166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127596 | GGAAAAAATATCAAA[A/G]TGAAATTAGTTTATT | 10277 |
rs549393168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175417 | AGCACTTTGGGAGGC[C/T]AAGGCGGGCGGATCA | 10277 |
rs549447061 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147444 | GTTGCATTGAGCCGA[A/G]ATCATGCTACTGCAC | 10277 |
rs549461269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066863 | GTGAGCCAAGATCAC[A/G]CTACCGCACTCCAAC | 10277 |
rs549465497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10090168 | TTTGTTGCCCAGGCC[A/G]AAGTGCAGAGGTGCC | 10277 |
rs549487942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141784 | TCATTATAGAAACTG[C/T]TTCTGCTAGCAAGCA | 10277 |
rs549506201 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067704 | TTGACCTTCCCAGAC[C/T]CAGGTGATCCTCCCA | 10277 |
rs549516957 | snp | A/G | 1.65699e-05 | 0.00287831 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106339 | CACAGTGCAGCCTCT[A/G]GAACTGCTGCGGGAA | 10277 |
rs549521524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064155 | CTCCCAATCTCTGCC[A/G]GCGCTCCTTTGTTCC | 10277 |
rs549532604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044155 | GGTTCAAGCGATTCT[C/T]GTGTCTCAGCCTCCC | 10277 |
rs549562102 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10082624 | TGTAGGTCCTATTAA[C/G]AAGGCGACTTTTTTT | 10277 |
rs549602625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082709 | GTTTGTTACATAGGT[A/G]CACATGTGCCATGGT | 10277 |
rs549654410 | snp | A/G | 0.000803858 | 0.0200321 | intron-variant | UBE4B | GRCh38.p7 | 1:10120233 | AAGCTTACATTTAAA[A/G]GTTTAGGCCGAGCAT | 10277 |
rs549692574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10059546 | GTATTCCCATTGTCT[A/G]TGAATTGAACAGGAG | 10277 |
rs549735381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075519 | CTGTGTAACAGCCCA[C/T]ATGCTGTTATCACAA | 10277 |
rs549753310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155885 | AAAGATTATCCGGGT[A/G]TGGTGGTGGGGGCCT | 10277 |
rs549770639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10148110 | CGGGTGCCTGTAGTC[C/T]CAGCTACTCGGGAGG | 10277 |
rs549773031 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180617 | GAATTTGAATTTCAG[-/T]TTTTTTTTTCTTTTG | 10277 |
rs549777823 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180504 | GTGCCTGCTACCAAG[A/T]GTTAATCCTGGGATC | 10277 |
rs549777856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148521 | CCTGTAATCCCAGCT[A/G]CTCGGGAGGCTGAGG | 10277 |
rs549807451 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108983 | AACCGTATCAGATTG[C/T]GTGCTGCTTTTACTA | 10277 |
rs549854772 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031965 | CGATCTCGGCTCACT[A/G]CAAGCTCCGCCTCCC | 10277 |
rs549877769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175453 | TCAGGAGATCGAGAC[C/T]GTCCTGGCTAACACG | 10277 |
rs549909828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111881 | AGAATCACTTGAATC[C/T]GGGAGGCAGAGGTTG | 10277 |
rs549932501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066639 | TGGCCAGGCAGGTGG[C/G]TCACGCTTGTAATCC | 10277 |
rs549936660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161396 | GATATGCGATCTGAC[A/G]TGCTGGGATTTTCCT | 10277 |
rs549966542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10055170 | AAAGCATCTTTTGGC[C/T]TGAAATGTTATGATT | 10277 |
rs549988745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129149 | AGGTTATCTTTGAGG[A/G]TAAAGCTTGAGTAAT | 10277 |
rs549990537 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142592 | AGGAGAATCGCTTGA[A/T]CACGGGAGACGGAGG | 10277 |
rs549993927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10153933 | ACTAAAAATACAAAA[C/T]TAGCCTGGCATGGTG | 10277 |
rs550011538 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086615 | TCAGTGGATCCATAG[A/G]AATTACACTTGTGTG | 10277 |
rs550012678 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163336 | CCATGGCCCCTGCTC[A/G]AGGATGACATGCAAA | 10277 |
rs550020487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052069 | ATGTCTAATAGTGTC[A/G]TTTTTTTTTTTTTTT | 10277 |
rs550037933 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106012 | AATGGGGACTTTATC[A/G]TCTTGTAAGTATAGC | 10277 |
rs550040316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092311 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTAAAG | 10277 |
rs550042552 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103894 | GCCTCCCAAAGTGCT[C/G]GGATTACAGGCATGA | 10277 |
rs550057390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10052683 | GCATATTCATTTGTC[A/G]TGGGGCCCTGAACAT | 10277 |
rs550155455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120394 | TGGGCATTGTGGCAT[A/G]TGCCTGTAATCCCAG | 10277 |
rs550223370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050222 | GATTACAGGCATGCA[A/C]CACCACACTTGGCTA | 10277 |
rs550240132 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084347 | ATTATAATCTAATCC[A/C/G]AGGGCTTGCAAGGTG | 10277 |
rs550334020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100232 | CTGACCTTGTGATCC[A/G]CCCACCTCGGCCTCC | 10277 |
rs550364874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075568 | GCATTCCCTAAACGG[C/T]TAGTTCTTGCCCGGG | 10277 |
rs550375490 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | UBE4B | GRCh38.p7 | 1:10066052 | CCCCCTCCTTCCCTC[C/G]CCCACTCCTTCCCTC | 10277 |
rs550378050 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113698 | CTGAGTTCACAGGCA[C/T]GCTCACATGCTGGCT | 10277 |
rs550392403 | in-del | -/TCAG | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10122270 | GCCCATTTCAACGAA[-/TCAG]TCAAACATCTATCTT | 10277 |
rs550403908 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068159 | TCAGCCTCCCAAGTA[A/C]CTGGGATTACAGGTG | 10277 |
rs550434924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175520 | GCCAGGCGTGGTGGC[A/G]GGCGCCCGTAGACCC | 10277 |
rs550454904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044605 | CTCCTTCCACCGCCC[A/G]CCTGTCTCGCTTTGT | 10277 |
rs550482885 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093624 | TGGAAGGGTTAAAAT[A/T]GTATTTATTCAGTGA | 10277 |
rs550518712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173800 | TCACAGGCGCTTAAC[A/G]TAACACACAGAAGGT | 10277 |
rs550537527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068913 | TTCCTAAATTTTCCA[A/G]CGGATCTTTAAGATG | 10277 |
rs550558000 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10067645 | TTTTTGAGACCCGGC[A/T]CTCACCGGGTTGCAC | 10277 |
rs550565298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074417 | AAAAGGAACTCTCTT[C/G]ATCTAATTCCCCCTG | 10277 |
rs550565436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10124906 | CGAGGCAGGTGGATC[A/G]CCTGAGCTCAGGAGT | 10277 |
rs550602406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116905 | CTACTTTACCTTTTT[C/T]ACTGATAGTTTTAGA | 10277 |
rs550610964 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10058296 | GGAAAGTGAAGCAGA[A/C]AATGATTGGAAAAAT | 10277 |
rs550613209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10145723 | TCTAGCCATGCATTT[C/T]CATGATATTTGACAA | 10277 |
rs550619371 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138340 | CTGACCTCGTGATCC[A/G]CCCGCCTCAGCCTCC | 10277 |
rs550631164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166740 | ACCAGCCTGGCCAAC[A/C]TGGCGAAACCCCAAT | 10277 |
rs550635997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109778 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 10277 |
rs550711974 | snp | C/T | 1.66399e-05 | 0.00288438 | intron-variant | UBE4B | GRCh38.p7 | 1:10168123 | TACTCAGCGTCTGTT[C/T]GATGTGTCCTAGGAT | 10277 |
rs550757735 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10154036 | ACGGTGAGCCAAGAT[C/T]GCGCCATTGTAATCC | 10277 |
rs550761305 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10043369 | TTTCTGAGATGTACT[C/G]TCCTCCCCCTTGTTT | 10277 |
rs550762355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078760 | TTTTCATCTTGACAG[G/T]ATTATTAGGTCTAGT | 10277 |
rs550797139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079510 | GATTACACAATTATA[G/T]AGGAATATAATTATC | 10277 |
rs550799066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10071536 | AAGGCTGCAGTGAGC[C/T]ATGATTGAAATACTG | 10277 |
rs550800916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124004 | GGTGTTGAATTCCTG[A/C]TGTCAGGTGATCCAC | 10277 |
rs550815085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10116209 | GTGCAGTGGCATGAT[C/T]TCGGATCACTGCAAC | 10277 |
rs550818218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111449 | CCTCACTCTCCTCAG[G/T]TCTATCAGAGGGTGG | 10277 |
rs550842386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065863 | ATTATAATGTAAATC[C/T]ACATCCTTTTAAAAA | 10277 |
rs550871153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146493 | ACTGCTTAAATGTAT[A/G]CATCAGTGTGTGCAT | 10277 |
rs550890321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080810 | AAATAAGCCAGGCAC[A/G]GAAAGGCAAATATTG | 10277 |
rs550899431 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10064184 | CCTCGTCTGCCTAAC[C/T]CCTACCTGTCCTGAA | 10277 |
rs550901625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10167385 | CGGAGGTTCCGGTGA[C/G]CCGAGATCGCGCCAT | 10277 |
rs550933705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10072453 | TTTTTTTTTCAAACA[A/G]GTTTAGGTATTATCT | 10277 |
rs550950125 | in-del | -/AA | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10070816 | ATCAAGTAAAAAAAG[-/AA]AATCTGATCATTTTG | 10277 |
rs550963020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037213 | TGTATTTTTAGTAGC[A/G]ACGGGGTTTCTCCAT | 10277 |
rs550983486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088388 | TTTTTAAATTTATTT[C/T]ATTTTTTTTTGAGAT | 10277 |
rs551029024 | snp | C/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10147299 | GGAGTTCAAGACCAG[C/G]CTGGCCAACATGGCG | 10277 |
rs551035354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148054 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs551046202 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178244 | ACCTCTTCTTTCTTA[C/T]AGGCTGCCAGGGCAC | 10277 |
rs551046856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10103262 | CCACTTTCTTCCCTT[G/T]CCACTGATCTTATCG | 10277 |
rs551074754 | in-del | -/AAAA | 0.00199601 | 0.0315281 | intron-variant | UBE4B | GRCh38.p7 | 1:10038282 | TGAAACTCCATCTCA[-/AAAA]AAAAAAAAAAAGATT | 10277 |
rs551081150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10168809 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA | 10277 |
rs551096599 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121555 | CACACCATCTTGCCC[A/G]GTTGATATTTTCATC | 10277 |
rs551120622 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144973 | AAATAATGAAAGCCA[A/G]TGGAAAGATTCCCCA | 10277 |
rs551206827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140722 | TGTTCACCTCATCTG[C/T]GTATTTTTCAATGCT | 10277 |
rs551207656 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10116999 | GTTCTATTGCCAAAT[C/G]TTAGATGAGGGCTTT | 10277 |
rs551207708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125750 | GAGCTAGGCTGAGTA[A/G]ATCTTACATGGTGTT | 10277 |
rs551271525 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038034 | GCCTGTAATCCCAGC[G/T]CTTTGGGAGGCCGAG | 10277 |
rs551271569 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069694 | TGTGTGGCACCATGC[C/T]TGGCTGATCTTTGTA | 10277 |
rs551291245 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162507 | GTGACGGGGTTTCAC[C/T]ATGTTGGCCAGGCCT | 10277 |
rs551321936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168855 | CGAGATGGTGCCACT[C/G]CACTCCAGCCTGGGC | 10277 |
rs551327136 | in-del | -/CCA | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10035893 | GACTACAGGCGCCCG[-/CCA]CCACCACGCCCGGCT | 10277 |
rs551415267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10051760 | GGACTAAAGAATACA[A/G]CCTGAGGTGACACAC | 10277 |
rs551449399 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166160 | AGCTCTGCCAGCTGT[C/G]TTCCTTTCCCAACAA | 10277 |
rs551472480 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142733 | TCTCCTTTGCCTTTT[C/G]CATCTTCTGAAAGCT | 10277 |
rs551500011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095679 | CCTCTAGTCCATAGT[C/T]AGAAATGCCAGCTAG | 10277 |
rs551509025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161644 | ACAAGAATTTGATTT[A/G]TTCCTATGGGCTTCT | 10277 |
rs551518207 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167932 | GCAGAGTTAAATAAG[A/G]CACCAACATCACCTG | 10277 |
rs551538406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088432 | GTTGCCCAGGCTGGC[A/G]TGCAGTGGCGCAATC | 10277 |
rs551562837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174318 | GAATAGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 10277 |
rs551569026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111927 | ACACCACTGCACTCC[A/G]GCCTGGGCAACACAG | 10277 |
rs551585021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072641 | CAGAACTTTTTCTTT[A/C]ACTTTTCAGAGGATA | 10277 |
rs551608579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10057556 | TGAGTAGGCACACAC[C/T]ACCATGCCAGGCTAA | 10277 |
rs551613550 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144836 | AAAGATGTTACAATG[C/G]GAAAACAAACAACTG | 10277 |
rs551622179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073418 | TTGAAATGTCTGTCT[A/C]ATTTCGAATTCATGA | 10277 |
rs551630060 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049360 | CAGTAAAGGGGGTAC[A/G]GTTGATGGGGCAGTT | 10277 |
rs551633759 | in-del | -/A/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173479 | GAGCAAGACTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 10277 |
rs551706007 | snp | A/C/T | 0.000148881 | 0.00862669 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168216 | CCTGGCCACCGAAAC[A/C/T]GTGGACATGTTCCAC | 10277 |
rs551707757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172509 | CCTTGAACCCATATC[C/T]TCAGTCTCTCTGCTG | 10277 |
rs551737400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069889 | TTAAGTGACTTATCT[A/G]GATAGGCTCCAGATA | 10277 |
rs551739094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052937 | AGATACCTGTTTTCT[C/T]ACTGTGTCCTCACTT | 10277 |
rs551743877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10179022 | AGCTTAGCCTGACTT[A/G]AAGCCAGATAACAAC | 10277 |
rs551779303 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120911 | TTCTAGGTGTTCTTA[C/G/T]GTTATTTTGTATGCC | 10277 |
rs551796891 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179193 | GGCTTTCTTCTCTGT[A/T]CCCTCCCCCCAGCAG | 10277 |
rs551832672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074475 | AAAACCTTTGCAGCA[A/G]AACTTCCGGAATGAG | 10277 |
rs551846875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046354 | GATCAACTTCAGAGT[A/C]CAGAATCCCTGGGTG | 10277 |
rs551854610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077682 | TGGCTGACATTGTTC[C/T]TCTCACCACAACCAG | 10277 |
rs551885730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162109 | GTTGAAGCGATTTTC[G/T]TGCCTCAGCCTTCTG | 10277 |
rs551898203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063491 | AATAACAGCCAAGTT[C/G]TGTTGGGAACACAGA | 10277 |
rs551914211 | in-del | -/TTTTC/TTTTCTTTTC | 0.0150938 | 0.0856851 | intron-variant | UBE4B | GRCh38.p7 | 1:10055278 | TTTCATCATTTTTTC[-/TTTTC/TTTTCTTTTC]TTTTCTTTTCTTTTC | 10277 |
rs551925154 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071537 | AGGCTGCAGTGAGCT[A/G]TGATTGAAATACTGC | 10277 |
rs551927258 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10113027 | GTGTTAGTCCATTTG[C/T]ATTGCCATACAGAAA | 10277 |
rs551949274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10047738 | ACCTCATGACCCACC[C/T]GCCTCGGCCTCCCAG | 10277 |
rs551974373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10088959 | GTCGGGATTACAGGC[A/G]TGAGCCACCACACCC | 10277 |
rs551984449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041184 | ACAGATAAGAAAATG[A/G]AGGCTAATAGAAATT | 10277 |
rs552006096 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10134337 | CCAATATGGTGAAAC[C/T]CCATCTCTACTAAAA | 10277 |
rs552009716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116162 | TTTTCTTTTATTTTA[A/G]GACAGCGTCTCTCTT | 10277 |
rs552022586 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086107 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 10277 |
rs552028542 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180269 | TTTTAGTGATGGCTA[A/T]TGGGTCTGGGCAGCA | 10277 |
rs552057145 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123210 | CTGAGGCGGATGGAT[C/T]GCCTGAGGTCAGGAG | 10277 |
rs552062052 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102201 | TTTACAAAATTCTTT[G/T]TTATATGCTGTTTTA | 10277 |
rs552072495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126538 | GGTTTTGTTGAATTA[C/T]TGGGGGTCCTGTCAG | 10277 |
rs552091766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176686 | TGGCCATTTTTATAT[G/T]TTCTTGGGAGCAATG | 10277 |
rs552102218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10171982 | ACCCCATCTTTTTAA[A/G]GGCCTTCTTGACAAA | 10277 |
rs552109620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127254 | GGCAAAGCTGTACAT[A/G]CTAAGAAAATGAATA | 10277 |
rs552111254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10118666 | TGAGCCACCATGCCC[A/G]GCTAATTTTGTATTT | 10277 |
rs552124474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094634 | AGAGACGGGGTTTCA[C/G]CATGTTAGCCAGGAT | 10277 |
rs552142552 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061340 | GCCCACTACAACCTC[C/T]GTTTCCTGGGTTTAA | 10277 |
rs552164244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164840 | TGTTTCTCAACGAGG[G/T]CACTAGTTGGAATTT | 10277 |
rs552195278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10130045 | ATAAGAAGAGTTCAT[C/T]TGAACTTCATCCAAT | 10277 |
rs552227630 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10162250 | ACGATCTCAGCTCAC[-/T]GCAATCTTTGCCTCC | 10277 |
rs552234480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086165 | TTTAGTAGAGATGGG[G/T]TTTCACCGTGTTAGC | 10277 |
rs552250240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10123206 | GAGGCTGAGGCGGAT[A/G]GATCGCCTGAGGTCA | 10277 |
rs552261570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10124956 | CATGGCAAAACCCCA[C/T]CTCTACTCAAAATAC | 10277 |
rs552268690 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174161 | AGCACTTTGGGAGGC[C/T]AAGGTGGGTGGATCA | 10277 |
rs552289127 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082335 | AGACGTTACCTCTAC[-/A]AAAAAAAATACACAA | 10277 |
rs552297419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10043744 | GGATGCTTCTTATAA[A/G]TAGATGGTGTAATCA | 10277 |
rs552335036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064096 | ACACACTCATTCTTA[C/T]CAACTACTCAGCGTT | 10277 |
rs552342989 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111163 | GAGTAAAATCCAAAG[C/T]CTCTGACCATGGTCT | 10277 |
rs552358558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10085788 | AGCCCTCCTGTATTC[A/G]GTGACTTTTTTTTTT | 10277 |
rs552394250 | in-del | -/ACTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113261 | ATCTCACGTGAACTC[-/ACTG]AGTGAGAACTCACTC | 10277 |
rs552434955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079756 | TAGTTCTGGGGTCTG[A/G]ATCAGAAACAGAATT | 10277 |
rs552438197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133758 | TCTACAAAATATACA[A/G]AAGTCATCTGGGCAT | 10277 |
rs552450372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10101539 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 10277 |
rs552457803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108790 | GTAAATTTCCCAAAG[A/G]TGAAAGTGTCTTTTT | 10277 |
rs552461109 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064654 | CTTTTCCTCTCTCAA[C/T]AGCCCTGGCTAGTCC | 10277 |
rs552489594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077196 | GGTGTTGGTAGGGCG[A/G]TGCCTCCCAATAAGG | 10277 |
rs552514749 | snp | A/G | 0.000362337 | 0.013455 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130577 | GAGACTCTCTTACTT[A/G]GGGGCTTTCTTTAGC | 10277 |
rs552515350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056584 | ATTCTAGTTGTTTGT[A/T]ATATTACCTTTATTT | 10277 |
rs552524411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10138238 | GAGTAGCTGGGACTA[C/T]AGGCGCCCACCACCA | 10277 |
rs552569508 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082803 | CTAATGCTCTCCCTC[C/G]CCTTGACCCCACCCT | 10277 |
rs552577521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177664 | CTGTCTCAAAATATA[G/T]ATATATATTTATAGT | 10277 |
rs552601827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042581 | GAACCCGGGAGGCAG[A/G]GGTTACAGTGAGCTG | 10277 |
rs552610916 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040186 | CTGGAGTGCAGTGGC[A/G]CAACCTCAGCTCACT | 10277 |
rs552635882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043299 | CAGGTGTGAGCCACC[A/G]CACCCGGCCAACTTT | 10277 |
rs552639764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10035712 | TGACCGGCCAGAGAT[A/G]GTTTTTTTATTTTTT | 10277 |
rs552690758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10178179 | AGAGTATGAACAATA[A/G]TGGATTGTTTTTACC | 10277 |
rs552695227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110060 | CTTCCCCCTTTCTCA[C/T]TGATCTTCCCAGAAT | 10277 |
rs552720159 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10055931 | CTCAAAAAAACAAAA[A/C]AAAACAAAACAAAAC | 10277 |
rs552720594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163384 | CCTTTAAAAATAAAT[A/G]TTAGGCCAGGGGTGG | 10277 |
rs552745720 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | UBE4B | GRCh38.p7 | 1:10048556 | GGAGACTGATAAGGA[A/C]CAGCCACTGAGGTTG | 10277 |
rs552759185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048493 | AGAGGACTGAGCCTC[C/T]ATCCATTCCAGCAAT | 10277 |
rs552802985 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059587 | CCCATTGAGCTCATG[C/G]AGTTCCCAGGAGACG | 10277 |
rs552832251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10164335 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 10277 |
rs552834316 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10144136 | GAAGCCTTTTACTGC[-/AG]AGACAGATGGTGTTT | 10277 |
rs552888172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062995 | AAATAGTGATGGCGA[A/G]TAAAACAGATGTTGG | 10277 |
rs552893875 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | UBE4B | GRCh38.p7 | 1:10150877 | GAAAAAAAAAAAAAA[A/C]TAGGCTGGGCGCAGT | 10277 |
rs552945992 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143566 | TCTTCCCATCTCAAA[G/T]CCATACCCTTAATCA | 10277 |
rs552948939 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10048259 | ATGGGGAAAATTGAA[A/C]GAGAAGATTGGGAGG | 10277 |
rs552949532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131549 | TTTTGATCATGGGAA[A/G]GAAGTAACAAAGCCT | 10277 |
rs552976129 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10116345 | ACAGGGTTTCGCCCT[G/T]TTGGTCAGGCTGGTC | 10277 |
rs552985574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041719 | TGTTTGTTTTTTAAG[A/G]CAGAGCCTCGCTGTG | 10277 |
rs553012954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10109299 | TGTTCACCACCGCAC[C/T]GTGCTGCCACCCACT | 10277 |
rs553026319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144118 | AGCCTATTAGGTGAT[A/G]GGGAAGCCTTTTACT | 10277 |
rs553046751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108220 | CGCCCCCCTGTTCAC[C/T]CCCATTGAGCTCAGT | 10277 |
rs553055704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109951 | TGGTCCGCCCACCTC[A/G]GCCTCCCAAATTGCT | 10277 |
rs553101600 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091044 | AAGTTGGATACTGCC[A/G]CCTAGAAGGTTGCTA | 10277 |
rs553104569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086356 | CAGGTGATCCACCCG[C/T]CTTGGCCTCCCAAAG | 10277 |
rs553202748 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181666 | ATACAAAAAATTAGC[C/T]GGGCGTAGTGGCAGC | 10277 |
rs553241795 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086939 | GGCCTCCCAAAGTGC[G/T]GGGATTATAGGCTTG | 10277 |
rs553271278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114915 | TTAAGGGATCCCACA[C/T]GGACCTGCCCAGCCT | 10277 |
rs553356940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166061 | TTCTTGACCAGGGAA[C/T]GGCAGGCCCCCCAGT | 10277 |
rs553362154 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098268 | GATATTAGAAAATCT[A/G]TAAATATCATCTACC | 10277 |
rs553363537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131588 | AAAACTGTAACTGCC[A/G]GCTGGGCGTGTTGGC | 10277 |
rs553371427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177745 | AATACAAATATATAT[C/T]ATCACTAAGCAAGTG | 10277 |
rs553380735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119412 | AGGAAGAGGAAAGCA[C/T]GCTGTTTACTGATGG | 10277 |
rs553388329 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10151056 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs553415903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064334 | TCCTGAAAACCTAAT[A/G]TAAGATGGTGAAAAA | 10277 |
rs553417454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112381 | ACTACTTTAAATATT[C/T]AGAAATATTTCTTTT | 10277 |
rs553498974 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10177080 | GCGTGAGCCACCGCG[C/T]CCAACCAGAAGAGTT | 10277 |
rs553499278 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10159983 | GTCCTGAACTTGCCA[G/T]GTTCCTGAGATCGAG | 10277 |
rs553541856 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131041 | CTGGGAACTGGTCCT[A/C]AGCTTAGTGGCCCGG | 10277 |
rs553543475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161668 | GGCTTCTCTAGGCAA[C/T]TGTGTGAATCACTCA | 10277 |
rs553582782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123757 | ATAACATCAAACCAC[C/T]GTTGTTGTTTTGTTT | 10277 |
rs553601982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137591 | CATGGTTTCCCTTGA[G/T]AACCAGGATCATTTA | 10277 |
rs553614234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138344 | CCTCGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 10277 |
rs553633675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035052 | CGCCCAGGCTGCAGT[A/G]CAGTGGCGCGATCTC | 10277 |
rs553682982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172943 | GACAGGATTCAGTAC[A/G]GTCCCACACTGTACA | 10277 |
rs553693297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133825 | GAGGCTGAGGCAAGA[G/T]GATCACTTGAGCCAG | 10277 |
rs553702763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075136 | CTTTGGAGGCTGTGA[A/G]GTTAGAACTGTTTAT | 10277 |
rs553711089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127778 | CTAGGAAGACAAGGT[C/T]CCTCTCCTCAAGGCA | 10277 |
rs553722617 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10128236 | GTTTCAGTGAGGAGC[-/T]TTTAGCATCTGATAT | 10277 |
rs553743125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039689 | AAGTGGCCCACCTGC[C/T]TCTGCCTGCCAAAGT | 10277 |
rs553765104 | in-del | -/CTTCCTTC | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10044552 | CCTTCCTTCCTTACT[-/CTTCCTTC]CTTCCTTCCTTCCTT | 10277 |
rs553772496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169279 | CCTATGTGGAGACAT[A/G]TTTACTTTACAATGG | 10277 |
rs553778542 | in-del | -/TTTTTT | 0.477345 | 0.103991 | intron-variant | UBE4B | GRCh38.p7 | 1:10101498 | CTGTTGGTCTTTTGC[-/TTTTTT]TTTTTTTTTTTTTTT | 10277 |
rs553781475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082005 | CAGGCGTGAGCCACT[A/G]TTCCTGGCCTATTCT | 10277 |
rs553816887 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033077 | AGCTACGCGCATCCC[A/C]TCCTCCCCCTCCCCC | 10277 |
rs553855689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171448 | TGTTTTCCTTTGAGT[C/G]TGAAGAGCAGATTTG | 10277 |
rs553876296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162414 | TCCTGACCTTGTGAT[C/G]CGCCTTCCTCGGCCT | 10277 |
rs553914569 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180759 | AGGGGTGTAAGTGTA[A/T]CAGGACTTATGTGAC | 10277 |
rs553921283 | in-del | -/ACACACAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166965 | CACACACACACACAC[-/ACACACAAAA]AAAAAAAATTAGCTG | 10277 |
rs553948589 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10068368 | TTCTTTTTTTTTTTT[G/T]AGCAGGAGTCTCGCT | 10277 |
rs553948726 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10060736 | CTGTGTATTTTAGAA[A/T]CCCTAGTGAGCTAGT | 10277 |
rs553980753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176008 | CCCTTGCCCCAGCCC[C/G]TGGCAACCACAAATC | 10277 |
rs554005653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141401 | GTTTGGGGTCATGAG[C/T]CAATCCGGTAACCTC | 10277 |
rs554027092 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180580 | AGATGACATGATTAA[C/T]AAAAAAGGCAAGATA | 10277 |
rs554038926 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10114082 | AAAAAAAAAAAAGAA[A/G]AAAAAAAAAAAAGAT | 10277 |
rs554047929 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051318 | TTGGAGTGATGTGAA[A/G]TGTGCATGGTGTAGT | 10277 |
rs554089049 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097052 | CAAAAAAAAAAAAAA[-/AT]AATAATAATAATAAT | 10277 |
rs554109252 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031378 | CACTGCGCCCAGCCC[A/G]GGAGTGACTGTTAAT | 10277 |
rs554117236 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164815 | TTCCCACTCATGCTC[C/T]CTAGGTTAGTGTTTC | 10277 |
rs554160773 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10092429 | AGAGTTTCACCATAT[G/T]GGCCAGGCTGGTCTC | 10277 |
rs554169798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113368 | GTGCTCCAACACTGG[A/G]GACTGCATTTCAATG | 10277 |
rs554185343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099905 | TAGGGCAATTGTTCA[A/G]TCGGGGATAAATGAT | 10277 |
rs554208643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106124 | TAAAAGCTTGATATT[G/T]TCTGTTTTAGTTAGT | 10277 |
rs554233744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175653 | GAGACTCCGTCTCAA[A/C]TAAATAAATAAATAA | 10277 |
rs554272982 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10081538 | CAAGTGATCCTTTTA[A/C]CTCAGCCTCCCAAGT | 10277 |
rs554297374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085115 | ACCTAGAGTTGAACG[G/T]TCATACCTGGAGAGC | 10277 |
rs554298395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083089 | TTCCATGTCTTTGCT[A/G]TTGTAAATAGTGCTA | 10277 |
rs554299124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155281 | TCTTCAGTCATAGAT[A/G]GATGACATCTGTACT | 10277 |
rs554358157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053705 | TTTTTTTTTGAGACA[A/G]GGTCTTGCTATGTCA | 10277 |
rs554371341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10099166 | AGAATTGCTTGAACC[C/T]GGGAGGCAGGGGTTG | 10277 |
rs554385059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106009 | TCGAATGGGGACTTT[A/T]TCGTCTTGTAAGTAT | 10277 |
rs554395175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046585 | GTACTGTGAGGTTCT[C/G]ACCTCGCCTTTCTGG | 10277 |
rs554433677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075219 | GTAACTGTGTTCCAG[G/T]AAAACTTCACTTACA | 10277 |
rs554444389 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080556 | ATCTGGCAGTCCCAC[C/T]GAGTATATATCCAAA | 10277 |
rs554456637 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047743 | ATGACCCACCCGCCT[C/T]GGCCTCCCAGAGTGC | 10277 |
rs554519211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136803 | ACACGCCTGTAATCC[C/G]AGCTTACTAGGGAGG | 10277 |
rs554521825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068457 | CGGGTTGAAGTGATT[C/G]TCCTGCCGCGGCCTC | 10277 |
rs554538078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10120795 | GTGAGCTGAGATCAC[A/G]CCACTTCACTCCAGC | 10277 |
rs554541471 | snp | A/G | 1.66004e-05 | 0.00288096 | intron-variant | UBE4B | GRCh38.p7 | 1:10119647 | TGCTTGACATTAGCA[A/G]GCAGAGAGCCCTAGC | 10277 |
rs554545185 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10169389 | CCTGTCATCAGCAGA[A/G]GCACTATTGCCACTC | 10277 |
rs554549690 | in-del | -/T | 0.000255538 | 0.0113006 | intron-variant | UBE4B | GRCh38.p7 | 1:10144915 | GGCTGTTTTCTTTCA[-/T]TTGACTGTTAGTCTT | 10277 |
rs554560519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061464 | GTTTCACCATCTTGA[C/T]CAGACTAGTCTGGAA | 10277 |
rs554560960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162497 | ATTTTTAGTAGTGAC[A/G]GGGTTTCACCATGTT | 10277 |
rs554582626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10130165 | TGCAACCTCTGCCTC[C/T]TGGGTTCAAGCGATT | 10277 |
rs554602322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10067572 | ATATGTTCTGTTTGT[A/G]ATAAAAAGTGAGGTT | 10277 |
rs554624287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155404 | CAAATGAGGAAACTG[A/C]AGCTTAAAAGGGTCA | 10277 |
rs554624288 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10163242 | GGCTAATTAAAAAAA[A/T]TTTTTTTATAGAGAC | 10277 |
rs554665164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041495 | TCCCGCCAGCATGCC[C/T]AGCTAATTTTTGTAT | 10277 |
rs554680775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164410 | GCTGGAGTGCAATGA[C/T]AGATCTTAGCTCACT | 10277 |
rs554699922 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10034359 | CTGTAGCAGAGACTG[A/T]ACGGGAAGCAAGTGG | 10277 |
rs554735358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156315 | TACAATTACAGCACC[A/G]TGCACTCTTGACCTC | 10277 |
rs554744860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039017 | GTGAGCCGAGATTGC[A/G]CCACTGTACTCTAGC | 10277 |
rs554774246 | in-del | -/GTGTGTGTGT | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10101977 | TGCTCTGCATTTAGG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 10277 |
rs554777835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123519 | TAGTAATTAGAATAC[A/T]TTTCCTATTCAAGAA | 10277 |
rs554804465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172811 | AAAATACATAGTCAT[A/G]TGCTGTTTCTGTCGA | 10277 |
rs554810837 | in-del | -/AAAAAAAA | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10089503 | GAGAACATGTCTCTG[-/AAAAAAAA]AAAAAAAAAAAAAAG | 10277 |
rs554828195 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10175524 | GGCGTGGTGGCGGGC[A/G]CCCGTAGACCCAGCT | 10277 |
rs554837459 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031460 | TGAGGATGACTGAAC[G/T]GTGAACATAATAAAA | 10277 |
rs554891553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169925 | GAAGCTGTGGCAGGA[G/T]AATCACTTGAACCCA | 10277 |
rs554913419 | in-del | -/TTTTCTTTTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055274 | CACCTTTTCATCATT[-/TTTTCTTTTC]TTTTCTTTTCTTTTC | 10277 |
rs554923498 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10042423 | GGATGCTGAGGCGGG[C/T]GGATCACGAGGTCAG | 10277 |
rs554930893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143740 | GGATAAGCAGAAAGG[A/G]GAACTAGTTGGTTTA | 10277 |
rs554943659 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033238 | CGACCAGTTCCCGCC[A/G]GGAGCAAAGGGTAGG | 10277 |
rs554959122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086011 | GAGTCTCGCTCTGTC[A/T]CCCAGGCTGGAGTGC | 10277 |
rs554981682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092989 | AAAATGAATTCAGAT[C/G]ATCTCTTTGATGCCT | 10277 |
rs554985619 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155955 | CTTGAACCGGGACCT[A/G]GGAGGTGGAGGTCGC | 10277 |
rs555021181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122559 | CTTCCTAATTATTTC[A/T]TTTGGTATTTATACA | 10277 |
rs555030582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10179224 | TAGCTGACAAAGAAG[C/T]GCCTTCCCCTTACAA | 10277 |
rs555058184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10114993 | AGTCGGCAGGGAGTT[A/G]GCTGCCTTGTTCCTT | 10277 |
rs555074844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070158 | GCATGCCTGTAGTCC[C/G]AGCTACTTGGGAGGC | 10277 |
rs555121014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10126071 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACGAGG | 10277 |
rs555133934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149958 | AGTCTGGGCAATGCA[G/T]CAAGTCTGCATCTCT | 10277 |
rs555178383 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087545 | GAATACTAGTCATTA[C/T]TTTGTAGAATGTCCC | 10277 |
rs555185834 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10054738 | GCGGGGCATTTTTTT[G/T]GGAACAGTACCCATT | 10277 |
rs555201560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10040514 | CCTCAGCCTCCCAGA[A/G]TGCTGAGATTGCAAG | 10277 |
rs555224675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047311 | CTTAGTAACTCCATG[C/T]CTGCTAGGGGGCCAG | 10277 |
rs555231444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10152753 | CATTGAACTGAGATC[A/G]CACCAGTGTGCTCCA | 10277 |
rs555260296 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050845 | TGTTGAGATTATAGG[C/T]GTGAGCCACCACAAC | 10277 |
rs555313915 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090740 | TTGAGGTTTCAAGGA[C/T]GCTTTTGACAATTCT | 10277 |
rs555318307 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10085259 | CCTATCCTTAGTGAA[A/G]CAAAACTCCTTTGTT | 10277 |
rs555320607 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132072 | GAGGCGCAGGTTGCA[G/T]TGAGCTGAGATTGCA | 10277 |
rs555325352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043495 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 10277 |
rs555349489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094756 | CATTTTATTATACTC[A/G]CTTTATCACATATTT | 10277 |
rs555399186 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147226 | CAAGGCGCAGTGGTT[A/C]ACGCCTGTAATCCCA | 10277 |
rs555466449 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072679 | CTGATAGGATGTTTA[A/G]AACTATCTCATTAAA | 10277 |
rs555521168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096901 | AAAATTAGCTGGGTG[A/T]GGTGTTGCATGCCTG | 10277 |
rs555537462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038228 | GAGGTTGCAGTGGGC[C/T]GAGATCACACCACTA | 10277 |
rs555551261 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10059030 | GGGCGGGCGGATCAC[A/G]GATCACCTGGCCAAC | 10277 |
rs555560129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089241 | CGATCTCTTGACCTC[G/T]TAATCTGCCCACCTT | 10277 |
rs555614542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050750 | TTTTATAGAGGTGGA[A/G]TTTCACTATGTTGCC | 10277 |
rs555646782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095760 | GATTTTGTATTATTC[A/G]GAAATATTCTTCATA | 10277 |
rs555654189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065509 | TGCAGGGGTAGTTTC[A/G]GCCCTGTGACTGTTT | 10277 |
rs555670368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118331 | GTGGGCATGTCTCCA[A/G]GGTTTTTTGTTTTTT | 10277 |
rs555713745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087814 | TCCTAAGTCCATCCC[A/T]CACTTAAGGGGTGGG | 10277 |
rs555722058 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166824 | CAGCTACTCAGGAGG[C/G]TGAGGCAGGAGAATG | 10277 |
rs555724117 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141902 | GCCTTAACTTTCAGA[C/T]AAGAGGTCCAGCAAA | 10277 |
rs555729299 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169099 | TGTTTGTTCTCAACT[A/G]GTAAGACCTGGTTCC | 10277 |
rs555785690 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10131967 | CAAAAAAAAAAACAA[C/T]AAAAATGCAAAAACT | 10277 |
rs555790085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172034 | GCCCGGTTTCTCAAG[G/T]GATCAGAATCTTCTT | 10277 |
rs555790277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045540 | ATGGTACAGTCTACA[A/G]TCTGACATATTTGAT | 10277 |
rs555797980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141491 | CCTGCTGACCCCTTT[C/T]AGACTTCCAGAACTC | 10277 |
rs555813012 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10154062 | AATCCAGCCTGGGCA[A/G]CAAGAGCAAAACTCC | 10277 |
rs555836385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104936 | GTATCTAAAGACCAA[C/G]AGTAAATCAACTGGG | 10277 |
rs555860906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10110737 | AAGCCTTATATGAGT[A/G]GAGAAAGGGAAAATT | 10277 |
rs555892800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074652 | CTTCTCCTGGAAACA[C/T]GTTTTTCTTTTGGCT | 10277 |
rs555899316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095857 | GCTCACTGCAATTTC[C/T]GCCTCCCAGGTTCAA | 10277 |
rs556029442 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105410 | ATTCCAGAATCTAAT[C/T]CAGGATACTGCATCG | 10277 |
rs556030521 | snp | A/G/T | 3.29681e-05 | 0.00405995 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072202 | CCAGCTACCTCCCCA[A/G/T]TAGGTGCATCAGGTA | 10277 |
rs556030535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10039446 | TTTTGTTGTTGTTTT[C/T]TGGGACAGAATCTCT | 10277 |
rs556033322 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161251 | GAAGTGCAGGAAGAG[A/G]TGAAGAACAAAGAAC | 10277 |
rs556059251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111603 | GAACATCCATTAGCA[A/T]CATTTGTTTAATGAA | 10277 |
rs556088542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140470 | TGTTAATTTTCTGTT[C/T]AAGTTTTCCTTATAT | 10277 |
rs556093861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081954 | TCCTGGGCTCAAGTG[A/G]TCTTCCCACCTTGGC | 10277 |
rs556121979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045741 | TGTGGGGGCCACCAA[C/T]TGGGGTTAGTGGTTG | 10277 |
rs556145823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037578 | TGTGTTTATTTTTGA[A/G]ATAGGGTCTGGCTCT | 10277 |
rs556158775 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10046414 | ACAAAGTTATCAGGG[G/T]CTCTGCTGTCCCCCA | 10277 |
rs556165702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074166 | AGGGAACCTCCATCA[C/G]CCTCAGTCATCACAT | 10277 |
rs556166585 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180991 | ACACACACAGACAAA[C/T]ACAGCCACACGCGCA | 10277 |
rs556181352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10048352 | GATGTGAAATAGGTT[A/G]TATAGGAGTTTGCAG | 10277 |
rs556217119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081282 | TCAGGCTGGTCTCCA[A/T]CTCCCGATGTCAGAT | 10277 |
rs556241988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090487 | AGGGAAGTTTTTAGA[C/T]TCTGTAGACCTAGAT | 10277 |
rs556248711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175575 | AGAATGGCGTGAACC[C/T]GGGAGGTGGAGCTTG | 10277 |
rs556274669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142199 | TTGTATCTTCACCAT[A/G]CAGCCCAATCAAAGA | 10277 |
rs556288648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134655 | ATATATGTCTTCTCA[G/T]TGACTTTAGGATACA | 10277 |
rs556324717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075074 | TGTTTTCTAGACCTG[G/T]ATTGGCAAACTCTTT | 10277 |
rs556337098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10066244 | GCCTCAGTCTCCCTA[A/G]TAGCTGGCACTACAC | 10277 |
rs556354625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154632 | CACCTGAGGTCAGGA[G/T]TTGGAGGCTTAGTCT | 10277 |
rs556371992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10176611 | CGTGGTATTTCATTG[C/T]GGTTTTGATTTGTAT | 10277 |
rs556377154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043536 | GGTTCACACCATTTT[C/G]CTGCCTCAGCCTCCC | 10277 |
rs556414026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10043971 | GAAACAGGAGGTGGG[A/G]TGTCCATTTGCTGTT | 10277 |
rs556453165 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079672 | GATCCTCTGCTCTGG[G/T]AGCAGAAATGAACAG | 10277 |
rs556510002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174689 | CTTGGGCAACAAGAG[C/T]GAAACTCCGTCTCAA | 10277 |
rs556525249 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10142543 | GGTCATGGTAGTGCA[C/T]GCATGTAGTCCCAGC | 10277 |
rs556559013 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10098957 | ATTATTTACATGTTG[A/C/G]CTGGGCACAGTGGCT | 10277 |
rs556588936 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10135456 | TAAAAATACAAAAAT[C/T]AGCTGGGCATGGTGG | 10277 |
rs556614924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091233 | TTTGTGAAGATGAAG[C/G]AAGAAAAAACCTGTA | 10277 |
rs556639219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177887 | CTGCCCATTTTACAC[G/T]CAAAGAACCTGGGCT | 10277 |
rs556677462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10047655 | CCGCCACCACACCTG[A/G]CTAATTTTTTCTATT | 10277 |
rs556688602 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10157200 | TTGTATTTTTATTAA[G/T]AGTAGAGGCGGGGTT | 10277 |
rs556699640 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049783 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGATGGG | 10277 |
rs556745273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138406 | CTGGCCCAATTTTTT[G/T]TATTTTTTGTAGAGA | 10277 |
rs556747517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055578 | CACCACACCCAGCCA[A/G]CATGGGGCAAAAGTT | 10277 |
rs556759570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094323 | AGGACATTGTTGAGT[C/T]CACTTGAATTTTTTT | 10277 |
rs556784053 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033351 | TGGAGACCGCGCTGC[C/T]TAGCTGGGTAACCTG | 10277 |
rs556790580 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148505 | GGTGTGGTGGTGGGC[A/G]CCTGTAATCCCAGCT | 10277 |
rs556796452 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10087004 | GTACTTAGGTATGCT[A/T]AAAGTGGACAAGACC | 10277 |
rs556813813 | snp | A/G | | | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107308 | AAGAAGATGATGATG[A/G]TGGTGATGGTGATGA | 10277 |
rs556825748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10076531 | TTACACACGTGAGCT[A/G]CCACGCCTGGCCAAG | 10277 |
rs556840658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104116 | AGGGATCCTGAGAGA[A/C]GTGTTCTGTATGAGC | 10277 |
rs556868168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151118 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 10277 |
rs556886353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063687 | AGTCAGGCGGATCAC[G/T]TGAGGTCGTCAGGAG | 10277 |
rs556909662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144659 | AGAATCACTTGAACC[A/C]AGGAGGCGGAGGTTG | 10277 |
rs556920637 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10105995 | TACTACATCATTCTT[C/G]GAATGGGGACTTTAT | 10277 |
rs556925194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10115660 | CATGTGTCCTTTAAC[A/G]AGAGGGATACATTCT | 10277 |
rs556929016 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122316 | TGCACTAGGTGCTTC[A/G]GGCAATATGAAAAAA | 10277 |
rs556943542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10130866 | AGATGAGCTCCAGAT[A/G]CAGAGCTTTTATTTT | 10277 |
rs556979883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10035153 | ACAGGCGCCCGCTAC[C/T]ACGCCCGGCTATTTT | 10277 |
rs557021706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102863 | ATCACTAATAATGAA[C/T]TAAATCAGAATAACG | 10277 |
rs557054616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094871 | TCTTGGCTCACTGCA[A/G]CGTCTTCCTCCCAGA | 10277 |
rs557085726 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062952 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAA | 10277 |
rs557159132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070929 | TCATTAATTTATTTT[A/G]GAGGTGGAGTCTCCC | 10277 |
rs557206867 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181231 | ATGGTGACACACGTT[C/T]AGAAGAAATCTTCTT | 10277 |
rs557213914 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177444 | TCAGTGAGCCGAGAG[C/T]GTGCCTCTGCACTCC | 10277 |
rs557222665 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094252 | AGGGCAACAAAGTGT[C/T]AGGTTTTTAATTTCC | 10277 |
rs557252267 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108875 | AGGAACCAGTTTCCA[C/T]ATGGTAAAAGTGCTG | 10277 |
rs557260981 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10072970 | TGTCTTCTTGATCTA[C/G]AATCGTGTCAATTAA | 10277 |
rs557267712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035741 | TTTTTATTTTTTATT[C/T]ATTTTATTTTATTTT | 10277 |
rs557323960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10042912 | CTTGAGGTAAACTCA[C/T]TCTTGAGCTGTTCCA | 10277 |
rs557336525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10153184 | AGATTCTGCAGTGCC[A/G]GCCCCAGAATCACAA | 10277 |
rs557345036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159498 | TAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 10277 |
rs557346197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174008 | TGGCACAGTGACACA[C/T]GGGGCTCCTTGAATG | 10277 |
rs557362881 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10084985 | TTAGGATTACAGGCA[C/T]GAGCCACTGTACCCG | 10277 |
rs557378210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131867 | CTGAGGCAGGAGAAT[C/T]GCTTGAAACCGGGAG | 10277 |
rs557405698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160280 | TTCTTCCATGCGTCA[A/G]TCTTTGTGATAAGGA | 10277 |
rs557408095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10152875 | ATCCCTCAGTCTGGG[A/G]ACCCAAGGGAAGAGC | 10277 |
rs557411577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10111081 | CACACACACACACAC[A/G]CACACACACACAGTC | 10277 |
rs557456662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146151 | ATGTGTTTCAAGGGG[A/T]TCTATAAACTGCTTA | 10277 |
rs557475062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058815 | GCAATGCCGACCCCC[G/T]GGACAGTATTGGATG | 10277 |
rs557493449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173581 | TTTAGAAACAGAAAG[C/G]AAGTCATAGCCTGCA | 10277 |
rs557520312 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10153343 | AGACCCCATCTCTAC[A/G]AAAAATTTAAAAATT | 10277 |
rs557521920 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10164362 | CAAAAAAGAAAAAAA[A/G]AAAGAAAGAAAGAGT | 10277 |
rs557527115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10102172 | AGTGCTTTATTTTGT[A/G]TAGTTCTTTAATGTT | 10277 |
rs557536666 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10050875 | CCGGCCTGCCTCCCA[A/G]TTCTAGTATTGCAAT | 10277 |
rs557537941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132253 | AGGCTCTTCTAAAAT[A/G]AGTAGAAGTGGGAGA | 10277 |
rs557551100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151989 | TTGGTCCGGGTGCGG[C/T]GGCTCATGCCTGTAA | 10277 |
rs557580389 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114863 | GCGAGACTCCATCTC[-/A]AAAAAAAAAGACACA | 10277 |
rs557589970 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077360 | TTCCCTCTTATGACA[A/G]CCACTGGATTAGGGA | 10277 |
rs557602732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080157 | CTGGGTGTGGTGGCT[C/T]ACGCCTGTAATCCCA | 10277 |
rs557605447 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10116468 | CCTTTATCATCTTCT[A/G]TATGTAGGTTTTTTG | 10277 |
rs557609533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166149 | CGGCCAGCTTCAGCT[C/T]TGCCAGCTGTGTTCC | 10277 |
rs557629326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158842 | GGTGAAACCCCATCT[C/G]TATTAAAAATACAAA | 10277 |
rs557660791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125190 | TGTGCAATGCACAAA[A/C]GGATAACTATACAAG | 10277 |
rs557661610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145380 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATGGA | 10277 |
rs557663539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152625 | CAACATGGAGAAACC[C/T]CGTCTCTACTAAAAA | 10277 |
rs557666579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10064382 | ACAAGCAAACTGCTG[A/G]TCGCATCTCCGAGGA | 10277 |
rs557684243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056790 | TCACTCACCCATTGC[A/T]CATGGTCTGGTCTCT | 10277 |
rs557706304 | in-del | -/AAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168905 | TCAAAAAAAAAAAAA[-/AAAG]AAGAAGAAAAAGCAT | 10277 |
rs557710065 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151748 | TAGTTAGGAATAGGA[C/T]AACCATTCCACCTAC | 10277 |
rs557725353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050558 | TTGAATTATTTATTC[A/G]CTTGGTGTAGCTCCT | 10277 |
rs557747260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10059644 | GCGTGGCTGCTTAGG[A/G]CAAGGCCGAGGCGTG | 10277 |
rs557748595 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094723 | ACAGGTGTGAGCCAC[C/G]ACACCCAGCCTCATT | 10277 |
rs557814750 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096065 | TATGAGCCACTGTGC[A/C/G]TGGCCCACTATACTT | 10277 |
rs557853375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096828 | TGGATCACTTGAGGC[C/T]AGGAGTTCAAGACCA | 10277 |
rs557900613 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | UBE4B | GRCh38.p7 | 1:10166978 | ACACACACAAAAAAA[A/C]AAAATTAGCTGGGCA | 10277 |
rs557913766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056265 | CTTTTGTACACACTC[A/G]TATTATTTAGATAAA | 10277 |
rs557921515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044123 | AGCTCACTGCAACCT[C/G]CACCTGCCAGGTGCC | 10277 |
rs557929365 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160381 | AGTATATGCGTTTTT[C/T]CTGTTCTAGTCTGGA | 10277 |
rs557961557 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10161850 | GATACTTCCTTGGTC[A/G]CTTATGAGGCCCTTG | 10277 |
rs557963324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064271 | AAATTGCTCTCTGGG[A/G]TGATTCAGTTATTAC | 10277 |
rs557970965 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10138874 | TTTTCTTCTCTATTC[C/T]GTTAATGTGGTTGAA | 10277 |
rs558011631 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10167447 | CGTCTCAAAAAATAA[A/T]AATAATAATAATAAT | 10277 |
rs558017474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10087095 | CTCATTCTGTTCTCG[C/T]CTGACGCATACAGGT | 10277 |
rs558031740 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054099 | CAGGATTTTTGACAC[-/AT]AAACATTTATTTCCA | 10277 |
rs558053281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102674 | CCTCGGCCTTCCAGA[A/G]TGCTGGGATTACAGG | 10277 |
rs558107000 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094411 | GGAACACCCGTATAC[C/T]CACCATCTAGATTCT | 10277 |
rs558188010 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10052141 | GTGCCATCTTGGCTC[A/T]CTGCAACCTCCGCCT | 10277 |
rs558203077 | snp | C/T | 6.59e-05 | 0.00573983 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147088 | GGACCCCGCATATCC[C/T]GAGTGAGTGTGCTTC | 10277 |
rs558211950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100083 | CGAGCTCTGCCTCCC[A/G]GGTTCAGGCCATTCT | 10277 |
rs558212030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160369 | GGTATATTGGTGAGT[A/G]TATGCGTTTTTCCTG | 10277 |
rs558228515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164212 | CAGGCATGGTGACAG[A/G]TGCCTGTAATCCCAG | 10277 |
rs558244852 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154202 | GAGCCAAGATCGCGC[C/T]ACTGCACTTCAGCCT | 10277 |
rs558248780 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100576 | TTTATTTATTTGAGA[C/T]GGAGTTTCGCTCTTG | 10277 |
rs558259916 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075905 | AAAAATTAGCGGGGC[A/G]TGATGGTGCACACAT | 10277 |
rs558290022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156996 | AACATAGTGAGACCC[C/T]ATCTGTAAAAAAATT | 10277 |
rs558301654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075865 | GAGACCAGCCTGGGC[A/G]ACATAGCAAAACCCC | 10277 |
rs558303393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139842 | CAAGTGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 10277 |
rs558304629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081125 | TGGCATACAATGGCA[C/T]GATCTTGGCTCACCG | 10277 |
rs558312851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132934 | ACAGGAGGGAATGTC[A/G]GGTCCTGGAGTTAGT | 10277 |
rs558315721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147479 | GCCTGGGCGACAGAG[C/T]GAGACTCTGTCCCCA | 10277 |
rs558334621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068585 | CGAACTCCTGACCTC[A/G]GGCCATCTGCCTGCC | 10277 |
rs558340225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073848 | TGTTTCATACCTTCT[C/T]GAGTGTGCAGTACCT | 10277 |
rs558351408 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10107580 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 10277 |
rs558376342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125353 | TTCCCCAGCTCCACA[C/T]CTGAGTGTTACTTCT | 10277 |
rs558416016 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032948 | CCTCCCTGACGGGGG[-/A]TCACGTGATCCCTTT | 10277 |
rs558431555 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068413 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGT | 10277 |
rs558438809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084887 | TTTTGTATTTTTAGT[C/T]GAGACAGGGTTTCAC | 10277 |
rs558468151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069369 | AGGCACTGGTGCAAC[C/G]GAAGTTCTTGCTTTT | 10277 |
rs558505228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10062308 | AAATACATTCGATGT[A/G]TGTTTTTTTGTTTGT | 10277 |
rs558517039 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10056632 | AGATAAGAAATATTT[A/T]GTCACTTTCTTATAA | 10277 |
rs558541061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054907 | TCTCCTGCCTCAGCC[G/T]CCCGAGTAGCTGGGA | 10277 |
rs558560237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162588 | GCTGGGACTACAGGC[A/G]TGAGTCACCGCGCCC | 10277 |
rs558562414 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065804 | AAATTTACTGTGTCA[C/T]TGCCATTTGCATTTA | 10277 |
rs558607535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150217 | CCTGGGCAACATACA[C/T]AAAAAAACCCAAATC | 10277 |
rs558678560 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10035001 | TGTGGGTTTTTTTTT[G/T]TTTGTTTGTTTTTTT | 10277 |
rs558684182 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038942 | GTACGCACCTGTAAT[A/C]CCAGCTACTCAGGAG | 10277 |
rs558687996 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10093072 | TATATTGCTACAGTA[G/T]TATTGTACACATACT | 10277 |
rs558718853 | in-del | -/TAG | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10126348 | AGATAGATAGATAGA[-/TAG]ATAGAAAGGAGGAAA | 10277 |
rs558795195 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10130294 | TGGCCAGGGTTGTCT[C/T]GGACTCCTGACCTCA | 10277 |
rs558823750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113980 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGATG | 10277 |
rs558828770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129580 | GAGGTAACGTGTCTG[C/G]GAGGCTCTCAACTGT | 10277 |
rs558834979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165886 | GCAGATCCTCCCTAA[C/T]GGAATCTAAGCTGCA | 10277 |
rs558859570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163291 | TTCAGCAGCACGTAT[A/G]CTAACATTGGAACAA | 10277 |
rs558863036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121533 | CAAGTAGCCAGGACT[A/C]CAGGCACACACCATC | 10277 |
rs558907980 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10146673 | AAGGGCCTCCCTGTC[A/G]CCACCCTCTCCTCAT | 10277 |
rs558938961 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158621 | TTACCACAAGATGCC[A/G]CTAAATGTGGGCAGG | 10277 |
rs558966313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10172870 | ATCATATTATAATAC[C/T]GTATTTTCACTGTAC | 10277 |
rs558972427 | in-del | -/AAT | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10173493 | TCAAAAAAAAAAAAA[-/AAT]TATATATATATATAC | 10277 |
rs558978987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115826 | CTGCATGTTAGTGTA[C/T]TGAACACTCTAGGCA | 10277 |
rs559000189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10085654 | GTAAAGGGTTATAGG[G/T]TTTTTTTTAACATCA | 10277 |
rs559000868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070992 | TCTCAGCTCACTGCA[A/G]TTGCCCTCCACCTCC | 10277 |
rs559009420 | in-del | -/TAT | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10044898 | TGTGCCCTTTATTTC[-/TAT]TATTATTATATTGTA | 10277 |
rs559019557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086305 | CAGAGACAGGGTTTC[G/T]CCATGTTGGTCAGGC | 10277 |
rs559035843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086086 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 10277 |
rs559057648 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10158112 | GATGTTGTCCTAATG[A/T]TGGGAGTTTTCCTAG | 10277 |
rs559062702 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10047578 | GCTCACCGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 10277 |
rs559082800 | in-del | -/TGTGTT | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10075209 | ATGAGCAAGTGTAAC[-/TGTGTT]CCAGTAAAACTTCAC | 10277 |
rs559095014 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10061859 | GTTACTTACTGTGTT[A/G]CTATACGTGTGTAGT | 10277 |
rs559095362 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079324 | CCACCACGCCCGGCT[A/G]ATTTTTTGTATTTTT | 10277 |
rs559113998 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10136824 | ACTAGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 10277 |
rs559134636 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10063812 | ACTCAGGAGGCTGAG[G/T]CAGGAGAATCGCTTG | 10277 |
rs559160963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10134672 | GACTTTAGGATACAG[C/T]TATGTTTGAAAGTTC | 10277 |
rs559187674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176439 | TTCTACAGCTGCCGC[C/G]CATTTGACATTCCCA | 10277 |
rs559200368 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171870 | TGGGCAACAGGGTGA[C/G]ACTCTGTCTCAAAAT | 10277 |
rs559200417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144408 | TGTAGTGCCATCCAT[C/T]CAAAGACACATCATT | 10277 |
rs559220836 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072908 | GTGCTAAGAGAACTG[C/T]ATTGATCATAATATC | 10277 |
rs559228563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092004 | TCCTCTCTCCTTGAC[A/T]CCCCAAAAGTGCTGG | 10277 |
rs559284995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040136 | CTTTTTTTTTTTTTC[A/G]TCTTTTGAGACAGGG | 10277 |
rs559290492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10176361 | TTGGGTCTACACTTG[A/G]GAGTGGGATTGTTGG | 10277 |
rs559302451 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10176989 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10277 |
rs559312082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115948 | TTGTGGGACCACTAG[G/T]GTATATTTGGTCCAT | 10277 |
rs559330930 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165546 | AATCCTGTGGTGAGA[A/G]CAGCCTACAGCACGC | 10277 |
rs559348014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108602 | CAAAAATAACTCCAG[C/G]CTATAAATAGAGACT | 10277 |
rs559353284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106873 | TCCTGTTGCCAGTGG[C/T]AGTTGAAATGCTATC | 10277 |
rs559371807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156463 | CAGGCTGGTCTCAAA[C/T]TCCTGAGCTCAAGTG | 10277 |
rs559394546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100132 | GTAGCTGGGCCTACA[A/G]GTGCCCACCACCATG | 10277 |
rs559413756 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133797 | GTGCATGCCTATAGT[G/T]TCAGCTACTTGGGAG | 10277 |
rs559413976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076939 | TTTAGTATAGACTGG[A/G]TTTCACCACGTTGGC | 10277 |
rs559435643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10150281 | TTTAAAAGTGACTCA[A/G]AAACGTGGTTTATTT | 10277 |
rs559436436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129899 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 10277 |
rs559446085 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033472 | TAGTAGTCTGTGGGG[A/C]GACTGGAGTGACCGA | 10277 |
rs559459821 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126072 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 10277 |
rs559527981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10136901 | CTTCTGCCTGGGTGA[C/T]GAGAGCAAAAGTCCA | 10277 |
rs559552442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101406 | GATAATATCCATCTG[C/T]TTTTGGTTCAGGGCC | 10277 |
rs559577149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113710 | GCACGCTCACATGCT[A/G]GCTGGGGGTGCTGCA | 10277 |
rs559608777 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166941 | AAAAAATAAATAAAT[-/CA]CACACACACACACAC | 10277 |
rs559637572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048891 | AATGTGGTGAGCTTA[G/T]CTTTTTCTGTTTTAA | 10277 |
rs559638099 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082300 | ACCCAGGGGTTTAAG[A/G]CTAGCCTGGACAACA | 10277 |
rs559639194 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072277 | TTTTTGTTAAGCTGA[C/T]GGTTGTGATGTTTCC | 10277 |
rs559641863 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115563 | AGGCTTGAGCCACCG[C/T]GTTTGGCCAATATCA | 10277 |
rs559642792 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173294 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 10277 |
rs559643622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077427 | TACGTCTGCTAAGAC[C/T]CTCCTTGCAAACAGG | 10277 |
rs559651090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150947 | CGGGCGGATCACGAG[A/G]TCAGGAGATCGAGAC | 10277 |
rs559691952 | snp | C/T | 8.26153e-05 | 0.00642657 | intron-variant | UBE4B | GRCh38.p7 | 1:10130472 | GGCCTGTTCAGCGGC[C/T]TGACTGGCTCTTCCA | 10277 |
rs559708069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118947 | GAGTGCAGTGGTGCA[A/G]TCTTGGCTCACTGCA | 10277 |
rs559708508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048469 | GAGTGAGCATAAATG[C/T]GGAAGACAAGAGGAC | 10277 |
rs559709738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122649 | ATAAAGCTGTGTACG[G/T]AGTCTTGAAGGTTTC | 10277 |
rs559711023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142754 | TCTGAAAGCTGCCTA[A/C]GTTCCTCTGCTCCTT | 10277 |
rs559724678 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100801 | TCAGGTGATCCACCT[A/G]CCTTGGCCTCCCAAA | 10277 |
rs559757871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063941 | AAAAGTACATCTTAC[C/G]TGGTTATTCCCCTGC | 10277 |
rs559763602 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144793 | TAAACTATGATTTGC[C/T]GCTGGTTGTAAGATA | 10277 |
rs559785456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070453 | AAATTAAAAAAAAAA[A/C]AAAAAAACCATTACC | 10277 |
rs559797439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056449 | GAGTGCTCTCTGGGA[A/G]TTAGGTACTGTCATA | 10277 |
rs559850950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069786 | ATGATCCACCGCCTC[A/G]GACTCCCCTCGGCCG | 10277 |
rs559863714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147997 | CTTTGGGAGGCCAGG[G/T]CGGGTGGATCACATG | 10277 |
rs559863751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10091516 | GTGGTATGATTATAG[C/T]CCACTGCAGCTTCTA | 10277 |
rs559866781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10153730 | TGAGGTGGGTGGATC[A/G]CAAGGTCAAGAGATC | 10277 |
rs559873387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122169 | ACTTTTGCCTGAATT[C/T]GAACATCCATGTGTT | 10277 |
rs559877671 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147401 | AGGAGGCTGAGGCAT[A/G]AGAATCGTTTGAACC | 10277 |
rs559886594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111348 | CTCCTGTTCTTTGCA[C/T]GTAATACTCCCTCCT | 10277 |
rs559894293 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10125758 | CTGAGTAAATCTTAC[A/G]TGGTGTTACCTGGTA | 10277 |
rs559895036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051818 | GTCTTCTGAAAGAAT[A/T]GTACCCCTCCCAGCA | 10277 |
rs559923727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10103862 | CGATCTCCTGATCTC[A/G]TGATCCGCCCGCCTT | 10277 |
rs559963479 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169350 | TGCTCTTACCTTCGT[G/T]ATGTGACTCTCTGTT | 10277 |
rs559970027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118504 | CACCACACCCAGCTA[A/T]TTTTTTTTTTTTCTT | 10277 |
rs560037421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157508 | AAAATAGTTGGGCAC[A/G]GTGGCTCACACCTGT | 10277 |
rs560041052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10073610 | CTGTAATTCCAACTA[C/T]AAGAGAGGCTGAGGC | 10277 |
rs560069277 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157045 | TTTTGAGACAGAGTC[G/T]TGCTTTGTCGCCCAG | 10277 |
rs560070105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164636 | TTTTCCTGTGTTAAT[A/G]GATGAAAAAGGCCCA | 10277 |
rs560082782 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10156992 | GGCAACATAGTGAGA[-/C]CCCCATCTGTAAAAA | 10277 |
rs560083219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169520 | AGCTCAGACACTGGC[C/G]TCCCTTAAAAGTTTG | 10277 |
rs560098563 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10049578 | ATAAGACCTTTTCTC[-/T]TAAAAAAAAAAAAAA | 10277 |
rs560098744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10038002 | TTAGAAAGTGTTGGC[C/T]GGGCGCAGTGGCCCA | 10277 |
rs560107260 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031712 | AGTAGTCAGGTTCCT[A/G]TTTTAAGCATGTAGC | 10277 |
rs560153635 | snp | A/C/G | 0.0268129 | 0.112804 | intron-variant | UBE4B | GRCh38.p7 | 1:10066311 | TTTTGTGGGATTGGG[A/C/G]GGGGAGGGGGTCTTG | 10277 |
rs560153706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059371 | AGTCTGAAGGACACT[A/G]TTGTCAGAGCTCTGC | 10277 |
rs560195255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170343 | CAAAAGCAAATTCTT[A/G]AAAAGCTAAGTATAT | 10277 |
rs560208244 | in-del | -/AAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073721 | AGATTCTGTCTCAAA[-/AAC]AACAACAACAACAAC | 10277 |
rs560232977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052427 | TAGCACACTGCTTTA[A/G]TGGACGTTTTTGGGA | 10277 |
rs560256634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175600 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 10277 |
rs560370813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076110 | GTTTAAAAAGCTGGC[A/G]TGAGGAAGGTGATGG | 10277 |
rs560376519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10037633 | CATGATCTTGGCTCA[C/T]TGCAACCTCTGCCTC | 10277 |
rs560378944 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094011 | ATGGTTTTTTTAAAC[-/AT]GTGTCATTTTCCTTT | 10277 |
rs560417997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068675 | ATTTTTAGTAGAGCC[A/G]GTGTTTCTCCATGTT | 10277 |
rs560421331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174784 | GTATTTTCTATTTAT[A/G]TTGGCCATAAGCTGA | 10277 |
rs560448886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075317 | GAAAACTAGAAGCAG[A/G]CCAGATTCTCACCAC | 10277 |
rs560494007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120125 | TTTGTTTTTAAAAAT[C/T]TTTTTTCTTTGCCTC | 10277 |
rs560514247 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113191 | GGCAGGTCACATGGC[A/G]AGAGCAGGAGCAACA | 10277 |
rs560524421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10113071 | TGAAAAGAGGTTTAA[C/T]TGGCTCATGGTACCT | 10277 |
rs560524463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10121115 | TACATCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 10277 |
rs560533862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045929 | ACATGAAGTGGCAGC[C/T]GCTTAAGCCAGATAG | 10277 |
rs560536456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10128167 | TCACCATATTATGTA[A/G]ATGTTCCTTCATGGG | 10277 |
rs560544053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134368 | ATACAAAAAATTTGC[C/T]GGGCGTGGTGGCGGG | 10277 |
rs560561038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098193 | AAAATAATACAATAT[A/G]ATATAAATATAGTAT | 10277 |
rs560634770 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10067922 | TTTAGTAGAGACAGG[G/T]TTTCACCGTGTTAAC | 10277 |
rs560727974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045042 | GATCATCAGGCATTG[A/G]ATTCTCCTAAGGAGG | 10277 |
rs560745619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090710 | CAGGTATGAGCCACC[A/G]CACTTGACCTTTTAT | 10277 |
rs560780461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083403 | TCTCCAATTTTGAGT[C/T]TTTAATGAACATTAT | 10277 |
rs560834719 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181003 | AAACACAGCCACACG[C/T]GCACACAAGTATAAG | 10277 |
rs560845003 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10175485 | TGAAACCCCATCTCT[A/G]CTAAAAATACAAAAA | 10277 |
rs560859723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10112548 | GGGATTACAGGCACC[C/T]GCCACCATGCCTGGC | 10277 |
rs560875031 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10053346 | AGTAGAGACGGGGTT[G/T]CACTGTGGTAGCCAG | 10277 |
rs560875600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134722 | TTTGCCAAAATTTCT[A/G]TTCATGTTATTTTAA | 10277 |
rs560909809 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151844 | AAGAGCACAAGTTGG[C/T]AGTGTTATCTGAATG | 10277 |
rs560911670 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126719 | GGACATTCAGTTCTA[A/G]CACCTTATTTGACAT | 10277 |
rs560923627 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10118584 | ATCTCGGCTCACCGC[A/T]ACCTCTGCCTCCTGG | 10277 |
rs560931627 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170930 | TCAGCCTGCAACATT[A/C]CATTAAGTATTAGAA | 10277 |
rs560957326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10148467 | TGAAACACCGTCTCT[A/G]CTAAAAATACAAAAA | 10277 |
rs560977520 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181255 | TCTTCTTTGAGTCTC[C/T]TCTCTTTTGTGGAAA | 10277 |
rs561008264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173375 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10277 |
rs561010035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10045984 | GTCTGGGTAGGAGGC[C/T]GGGGCTGGTATGGCA | 10277 |
rs561023820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155828 | AGGAGTTTGAGACCA[A/G]CCTGGCCAACATGGC | 10277 |
rs561059510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090877 | TAAAGGTAGATATTT[A/G]GTCTAGTTTGTACTT | 10277 |
rs561067903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142307 | ATTATCTTAGTTTCC[C/T]ATGACTGCAACAACA | 10277 |
rs561085952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156618 | ATTGGGGCATTTTAG[A/G]TGATATGAGGCGTTG | 10277 |
rs561089520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171474 | ATTTGGGCTGGGCGC[A/G]GTGGCTCAGGCCTGT | 10277 |
rs561103275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168644 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGCCCA | 10277 |
rs561113118 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175527 | GTGGTGGCGGGCGCC[C/T]GTAGACCCAGCTACT | 10277 |
rs561135716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127153 | TATGAAAAAGATAAC[A/T]TATCTCCTAGCAATG | 10277 |
rs561137363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134932 | AGAGTGAGACCCCAT[C/G]TCAAAAAAAATTTTT | 10277 |
rs561142272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161376 | GCTGCATTTGTGGGT[C/T]TGATGATATGCGATC | 10277 |
rs561149442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128333 | GCCATTATTGATGCT[G/T]GCATAATAACGAGGA | 10277 |
rs561169992 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031901 | TACATATATATATAT[A/T]TTTTGAGATGGAGTC | 10277 |
rs561211414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10129074 | ACTTTTTTGTAAAAA[A/G]CATATATAGATACAG | 10277 |
rs561224683 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069223 | CCAACAATAGTGGGT[A/G]TGCTCTTCCAATGAT | 10277 |
rs561235244 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060296 | CTCCTTGGATACTTA[C/G/T]GGTATGGCCTAGGTA | 10277 |
rs561292687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068879 | TGGGCAGCCCAGAAC[A/G]CTGCCCCCTGCATGG | 10277 |
rs561332738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121208 | TAAAAATACAAAAAT[C/T]AGCCAGGCGTGGTGG | 10277 |
rs561338737 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10175616 | AGATCGCGCCACTGC[A/T]CTCCAGCCTGGGCGA | 10277 |
rs561341847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039828 | AGGGTAGTTTGGGAG[A/T]AGGTGGCTGCAGACT | 10277 |
rs561347995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175493 | CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA | 10277 |
rs561353406 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10034158 | TAAGCTTGATTAAAC[-/AT]ATATTTTTGCTTGAG | 10277 |
rs561364032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091613 | CCATGCCTAATTTTT[A/T]TTTTTTTTTTAAGAT | 10277 |
rs561369237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113758 | AGCTGGCAAGGACCT[A/G]TTGACATCAAACATA | 10277 |
rs561379133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107169 | GCAAAAGCTTCTCCC[C/T]GTCTTGTTTTTTCTT | 10277 |
rs561380508 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032593 | GTGTTTCTAGGCCCC[A/C]AAGTCACAGAAAAGC | 10277 |
rs561422676 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10159123 | GAAGTTGTCAGAATG[A/T]GTGAAATGAAATCTT | 10277 |
rs561425450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083484 | TTTTATGGTAAGTTG[C/T]CTTTGGCTAAGAATG | 10277 |
rs561426927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10167081 | AGGTTACAGTGAGCC[A/G]AGATTGTGCCACTGC | 10277 |
rs561442479 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048721 | TGGAGGCCCTTGGTT[A/T]CCTTGACAAGACTGA | 10277 |
rs561454383 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10052521 | GAATCATGTCTGTGA[A/T]CATGGTCTTTTGTTA | 10277 |
rs561480040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057402 | CTCCCTGAGAAAATA[A/C]CATTTACAGTCTTTT | 10277 |
rs561519611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039226 | ATGAGAAGGGACCCC[A/G]GGAGAGGCAGGGTCT | 10277 |
rs561524219 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130126 | TCACCCAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 10277 |
rs561544034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084524 | GTGCATTTGTCTGGT[C/G]TTCCAAACTAGATTG | 10277 |
rs561546600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10138524 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCTAAAAT | 10277 |
rs561607455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10036039 | GTGAGCCACCGCGCC[C/T]GGCCGAGGTAGTTTT | 10277 |
rs561627287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170528 | GTGGGTACTGAGTCA[C/T]CTTGTGAGATTACAG | 10277 |
rs561647494 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098360 | CCACATTAATTCATG[C/G]TAATAAGAAAATGAG | 10277 |
rs561717364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117755 | AACTTAGGATGTGTC[A/G]ATGAACAAAACAGAG | 10277 |
rs561717962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10042431 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGTTCGA | 10277 |
rs561764854 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081529 | TCCCAGGCTCAAGTG[A/T]TCCTTTTACCTCAGC | 10277 |
rs561816416 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085669 | TTTTTTTTTAACATC[A/G]GTTCTATCATTTTAC | 10277 |
rs561827640 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10081484 | GGCTGGAGTGCAGCA[A/G]TGGAATCTCGAATCA | 10277 |
rs561829404 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059856 | TGGCACCTCTGGGGC[A/G]TAGGTCTTCAGCCCA | 10277 |
rs561836475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173761 | GTGCGCCCTCTCCAG[G/T]GTGGTTGTGCTGTGG | 10277 |
rs561858298 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112462 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 10277 |
rs561862840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082227 | TACCCAGCTGGGCAT[C/G]GTGGCTCATGCCCGT | 10277 |
rs561865105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122426 | TTGCCAGATAAGTAG[C/T]GTCAAAAATTCATTC | 10277 |
rs561900555 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153963 | GCACATGCCTGTAAT[-/C]CCCAGCTACTTGGGA | 10277 |
rs561906539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086703 | TCCCTCTCTCTTTTC[C/T]CTTTTTTTTTTGAGA | 10277 |
rs561929913 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142595 | AGAATCGCTTGAACA[C/T]GGGAGACGGAGGTTG | 10277 |
rs561942010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078587 | GGTTATTTTATTTTA[C/T]AGCCTTGTTTTGGAA | 10277 |
rs561943863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087229 | AGGTAAAAATATTAA[A/G]TAAGAAGACTTAAGA | 10277 |
rs561946111 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077288 | GGCAACATAACTCCA[A/G]TCTTCACGTCCGTCT | 10277 |
rs561946946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177320 | AGGTCAGGAGATCGA[A/G]ACCAGCCTGGCCAAC | 10277 |
rs561956037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051107 | AAACTCCTGGGCTCA[C/G]ATGATTTTCCCGCCT | 10277 |
rs561967349 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035730 | TTTTTTATTTTTTTT[A/T]ATTTTTTATTTATTT | 10277 |
rs561980164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079456 | TGAGCCACCGCACCC[A/G]ACCTCAAAATTTACT | 10277 |
rs562001836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126368 | AGAAAGGAGGAAATA[C/T]TGGAACATTTAATTG | 10277 |
rs562049184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088314 | GGTTTTCTTATCCCA[A/G]TATTTAAGATACCAT | 10277 |
rs562054754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140679 | GCTTGCAGCAGATAG[C/G]CTTTATTGTGCTTTC | 10277 |
rs562091837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153026 | CTAGCTCTGGGGGTA[C/T]GAGACAAAGCTGAAA | 10277 |
rs562100868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044201 | TAGGTGTATAGGTGC[A/G]TGCCACCATGCCCGG | 10277 |
rs562133658 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10037888 | TGTTTTTCGACAATG[G/T]TAATGAGATTGCATA | 10277 |
rs562187409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086266 | ATGAGCCACTGCGCC[C/T]GGCCAATTTTTTGTA | 10277 |
rs562210411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095261 | CATATGAAGTATATT[A/G]ATAACTTATGATTTC | 10277 |
rs562254030 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE4B | GRCh38.p7 | 1:10060136 | ATGTAACCTACATGG[C/T]GATTTAAAACAAGCA | 10277 |
rs562256476 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10110574 | AAAAAAAAATTACCC[A/C]ATGGTAAAGGTACCG | 10277 |
rs562265539 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135354 | CTCATACCTATAATC[C/T]CAGCACTTTGGGAGG | 10277 |
rs562292919 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167331 | GTAGTCCCAGCTACT[C/T]GGGATGCTGAGGCAG | 10277 |
rs562294684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10043715 | TTACAGGCGTGATCC[A/C]ACGCGCTGGGCCGGG | 10277 |
rs562321597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10153617 | CTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGACC | 10277 |
rs562328945 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152881 | CAGTCTGGGGACCCA[A/C/G]GGGAAGAGCCTGGGG | 10277 |
rs562333492 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10103689 | AGGCTGGAGTGCAGT[C/G]GCGCAGTCTTGGCTC | 10277 |
rs562335213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131983 | AAAAATGCAAAAACT[A/G]GCTGGGTGTGGCGGC | 10277 |
rs562350701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058298 | AAAGTGAAGCAGAAA[A/G]TGATTGGAAAAATGA | 10277 |
rs562375458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10110665 | AAATTTGGTGGTTTT[G/T]TGTTTGTTTTTTAAC | 10277 |
rs562409505 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062621 | GGCCGCCTTAATGCA[-/T]TTTTTTGTTAATCAC | 10277 |
rs562415201 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175399 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 10277 |
rs562430145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147177 | TTGATAACTAAAACC[A/G]AAACCCTTTCTTTAT | 10277 |
rs562477127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10167868 | TGCTGGGATTACACG[C/T]GTGAGCCACCACGCC | 10277 |
rs562500097 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070376 | GATTACTCATAGTTG[C/T]AAGTATACAACCCAG | 10277 |
rs562528867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036328 | AACTTTTTTCAAGGT[C/G]AACAGAATATTAAAA | 10277 |
rs562537524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118462 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10277 |
rs562566037 | in-del | -/AAGGGGGCAGCCAGGAACAGACCC | 0.00993419 | 0.0697739 | intron-variant | UBE4B | GRCh38.p7 | 1:10133055 | GACGGACCAAAACAG[-/AAGGGGGCAGCCAGGAACAGACCC]AAGGGGGCAGCCAGG | 10277 |
rs562577224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10103748 | CAATTCTCCAGCCTC[A/G]GCCTCCCGAGTTGGG | 10277 |
rs562650204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10167177 | GGGCACGGTGGCTTA[C/T]GCCTGTAATCCCAAC | 10277 |
rs562708221 | snp | A/G | 9.91195e-05 | 0.00703917 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178773 | ATAGTGGCCAAGAAC[A/G]CACGCGCAGAAATCG | 10277 |
rs562721475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051748 | TTCTGCATATCAGGA[C/T]TAAAGAATACAGCCT | 10277 |
rs562726723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036981 | AGGAACTTTTAAATT[A/T]TGTGCACTTTTTGGT | 10277 |
rs562731865 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10081205 | GTAGCTGGGATTACA[A/G]GCCTGTGCCACCATG | 10277 |
rs562737257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173838 | TGGGTGGGCACAGCA[C/T]GCCCAGTGAGGTGAT | 10277 |
rs562758271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044252 | GGAGACGGGGTTTTA[C/T]TCTTGTTGTCCAGGC | 10277 |
rs562764156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147650 | TTTCTTTAAAATTTG[C/T]TATAAAGTCTTTGAT | 10277 |
rs562766499 | snp | A/G | 0.000118814 | 0.00770669 | intron-variant | UBE4B | GRCh38.p7 | 1:10072486 | GATGACAAGATGATT[A/G]AGACTGAATTTGGTT | 10277 |
rs562768191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080452 | AGAAAGAAAGAAAAT[G/T]CTATGTTGGTGAGAG | 10277 |
rs562796328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044742 | GCACGCCATCATGCC[C/T]GGCTAATTTTTTGTA | 10277 |
rs562796336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10179762 | CCCTCTCATGTCCCA[A/G]TCCTTCTGGAGTCTT | 10277 |
rs562802128 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031579 | GTCACCAGGGGTTCA[A/G]GTTCTGGCTTACACA | 10277 |
rs562838607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10083271 | TGGATATCTGTGGGG[C/T]AATCTTTGCAGACAG | 10277 |
rs562853609 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160123 | GGCATCTCCAGAGTC[-/T]TAACAGAGGTAGGCC | 10277 |
rs562858250 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180246 | CACAGTTTGGGGCAA[C/T]GGAAGTCTTTTAGTG | 10277 |
rs562884979 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10038536 | TAACTTGTCCATAGC[C/G]ACCTGGCTTAGAAGT | 10277 |
rs562899018 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155881 | TACAAAAGATTATCC[A/G]GGTGTGGTGGTGGGG | 10277 |
rs562918547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162084 | TCTCACTGCAATCCC[C/T]GCTTCTCCGGTTGAA | 10277 |
rs562938875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10127874 | AAAACAGAGCTGTAC[A/C]CAAAGGGTGTATTTA | 10277 |
rs562954810 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBE4B | GRCh38.p7 | 1:10055796 | GTGGTAGCACGTGCC[C/T]GTAGTCCCAGCTACT | 10277 |
rs562956627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10052317 | GCTCAAATGATCCTC[C/T]GGCCTTAGCCTCCCA | 10277 |
rs562980529 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10176559 | TAAACATGTTAATTT[G/T]TTTTTGTTTCTTAAA | 10277 |
rs562993587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037922 | GATTTTTCTCTCCTA[A/T]CTCTTCTTTATGACC | 10277 |
rs563026405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10088946 | AACCTCTCAATGTGT[C/T]GGGATTACAGGCGTG | 10277 |
rs563075430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070502 | TCCTGCCTCTCCCGA[A/G]CTGCTTCCTGCCCCT | 10277 |
rs563111810 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10055082 | TGAGCCACCGCACCC[C/G]GCGTGTTTTTACTTT | 10277 |
rs563120688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041786 | ACTGCAACCTCCGCC[A/T]CCCGAGTTCAAGTGA | 10277 |
rs563171122 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073382 | GAAAAACTCAGAACC[A/G]TTTGAACTAATTGAA | 10277 |
rs563185159 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043194 | TTGTATTCTTAGCAC[A/G]GTTGGAGTTTTACCA | 10277 |
rs563207126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133519 | AAGTTACATTGTTAT[A/G]TTGCTAATGCAGGAG | 10277 |
rs563216446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089413 | CAGAAGTCTGAAGCA[A/G]GAGGATCATTTGAGC | 10277 |
rs563250504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173117 | ACTGTGTGTCTAAAG[C/T]AGTTTTATCATACAA | 10277 |
rs563264465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10136944 | AAATAAATAAATAAA[C/T]AAATAAAAAGTATCT | 10277 |
rs563339393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131306 | ACATGACGAAACCCC[A/G]TCTCTACTAAAAATA | 10277 |
rs563396191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172474 | GGGACAGAGGCATGA[A/T]CCATGTCCAGGCAGC | 10277 |
rs563449059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034627 | CCTACCTCCACATTT[C/G]TTCACTGGTTCATCA | 10277 |
rs563456029 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10093229 | ATTGATTAATTTTAA[C/G]TAAAAAGTTACTTGG | 10277 |
rs563457401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066641 | GCCAGGCAGGTGGCT[C/T]ACGCTTGTAATCCCA | 10277 |
rs563466209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144208 | TAACCTCAGAGAAGA[C/G]CATTGCGAGCAGAGG | 10277 |
rs563508898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071212 | ACCTGGCCAATTGGC[C/T]ATTTATTTTTAAATC | 10277 |
rs563528391 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053211 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCGCTG | 10277 |
rs563591360 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10056707 | TGCAGCTGGGATCCT[C/G]GCCAGCGCTAGCTAC | 10277 |
rs563603740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136550 | AGGTAGGACAGAATA[C/T]GGTGGTCCTTGAATG | 10277 |
rs563627824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152112 | AAATAGAAAAAAAAA[A/T]TAAATTAGCCGGGCA | 10277 |
rs563650579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10101489 | AGAATTCTTTCTGTT[A/G]GTCTTTTGCTTTTTT | 10277 |
rs563669387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057159 | ATATTTTAAGTATTA[C/T]GGGTGACTTAAGAAA | 10277 |
rs563673770 | snp | A/G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110729 | AATGTCACAAGCCTT[A/G/T]TATGAGTAGAGAAAG | 10277 |
rs563682343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042511 | AATTAGCCGGGCGTG[G/T]TGGTGCACGCCTGTA | 10277 |
rs563705841 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118527 | TTTTTCTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 10277 |
rs563727043 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10123805 | TGAGATGGAATTTTG[C/T]TCTTGTTGCCCAGGC | 10277 |
rs563727976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10035282 | GATTACAGGCGTGAG[C/G]CACCGCGCCTGGCCT | 10277 |
rs563770856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173295 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 10277 |
rs563782262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143288 | GTGTCTATAATTCCA[A/G]CTACTTGGGAGGCTG | 10277 |
rs563794689 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077735 | TGTGCTGAGTGCTGA[A/C/G]CAGAATTTTAAAAAT | 10277 |
rs563815239 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143316 | CTGTGGCAGGAGAAT[A/C/T]GCTTCAACCCGGGAG | 10277 |
rs563817998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043220 | TACCATGTTGACCAG[A/G]CTGGTCTTGAACTCC | 10277 |
rs563835592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173718 | TCTTCCATCGTTGCC[A/G]TAGAGAGACTTGGAA | 10277 |
rs563848721 | in-del | -/TCTGGCT | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10176116 | GTGTAACCTTCTATG[-/TCTGGCT]TCCTTCACTTAGCAT | 10277 |
rs563864514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064154 | CCTCCCAATCTCTGC[C/T]GGCGCTCCTTTGTTC | 10277 |
rs563889388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078570 | ACTTCTTAACTGTCT[C/T]GGGTTATTTTATTTT | 10277 |
rs563895335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151171 | CTGTCTCAAAAAAAA[A/G]AAAAAGTCACTGTAA | 10277 |
rs563896947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144292 | TTGAATAGGCAAAGT[A/T]ACCTCGAATTTTCAT | 10277 |
rs563902327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115417 | GGGATTACAGGCACA[C/T]GCCACCATGCCTGGC | 10277 |
rs563916190 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105892 | ATTTAGTCATTGGAA[C/G]TGGAATTCTCTTTTC | 10277 |
rs563959231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10041896 | AGAGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 10277 |
rs563959367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10144794 | AAACTATGATTTGCC[A/G]CTGGTTGTAAGATAT | 10277 |
rs563990154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034744 | AGTACTTAGTGTGTT[C/T]ACTTAGGGACTGAAA | 10277 |
rs563994397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042387 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs564012900 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151482 | TGTTCAGCCACGAAC[C/G]CAGAAGTTTTTTGAA | 10277 |
rs564024299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116182 | GCGTCTCTCTTTGTC[A/G]CCCAGGCAGGAGTGC | 10277 |
rs564032298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10166348 | TGCGCCAGAGGTAAG[C/T]GTGCTGACAGTTCTG | 10277 |
rs564032600 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126582 | ACCAAACTCCTCTTA[C/T]TTCTGGAGAATTCAG | 10277 |
rs564059581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177228 | GTACTTTATGAAGAA[A/G]AGAGGTTTAGGCCGA | 10277 |
rs564061544 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE4B | GRCh38.p7 | 1:10052781 | TAGTTCATTTGGACT[A/G]TTATAACAAAATGCC | 10277 |
rs564088613 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10123881 | CGGGTTCAAGCGATT[C/T]TCCTGCCTTAGCCTC | 10277 |
rs564104156 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136816 | CCCAGCTTACTAGGG[A/G]GGCTGAGGCAGGAGA | 10277 |
rs564160612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111778 | CCTGGCCAACATGGC[A/G]AAACCTCTTCTTTAC | 10277 |
rs564160746 | in-del | -/A | 0.106236 | 0.204528 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181268 | TCTTCTCTTTTGTGG[-/A]AAAAAAAAAAGGGCA | 10277 |
rs564180151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094914 | TCCTGCCTCAGCTTC[A/C]TGAGTAGCTGGGATT | 10277 |
rs564215414 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10175359 | ACCTACTTAGAAAAT[-/A]AAAAAAAAATAGCCG | 10277 |
rs564226108 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046460 | GTTAGGATAATGGAA[A/G]TAGAAAGTCCTGTTT | 10277 |
rs564245251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086470 | ATGTAGAGATAAATG[A/G]GGTATGGGGGGACTC | 10277 |
rs564264312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10088613 | ACTCCTCAGCTGATC[C/T]ACCTGCCTTGTCCTC | 10277 |
rs564305307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064489 | TTAAGGATACAGGAG[A/T]CTTCTTTCTGAACCT | 10277 |
rs564326522 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137094 | CTCCATTTTCTGAGC[C/T]GAAATTCCCTACGGA | 10277 |
rs564347181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139522 | GTGATGAAGTTGTCA[A/G]GGCTTAAGAGTTTTC | 10277 |
rs564358240 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093887 | TTAACTAGAAACAGG[G/T]TTTCACCACATTGGC | 10277 |
rs564389182 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142341 | TACCACAACTTTAGT[C/T]ACTTAAAACAACACA | 10277 |
rs564391397 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070791 | AAGTGGCAGATTGTA[C/T]TTTTATTGAATCAAG | 10277 |
rs564410997 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039597 | CCATGCCCTGCTGAT[-/T]TTTTTTTTTTTTTTG | 10277 |
rs564417361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10178917 | TAATTTTTTAATGGT[A/G]TGCTAGAGCTGCTTT | 10277 |
rs564441984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094635 | GAGACGGGGTTTCAC[C/T]ATGTTAGCCAGGATG | 10277 |
rs564449171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10043304 | GTGAGCCACCGCACC[C/T]GGCCAACTTTCAGTA | 10277 |
rs564484890 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10043621 | TTTTAGTAGAGACGG[C/G]GTTTCACCGTGTTAG | 10277 |
rs564527660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057235 | CAGCTGGCAGAATGG[A/G]GTTAGGCGTGTTTAA | 10277 |
rs564529014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037088 | GCTGGAGTGCAATGG[C/T]GCGATCTTGGCTCAT | 10277 |
rs564552821 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10109517 | CAGATTTTGGCAGCT[G/T]ATAGGTTCTTAGTTG | 10277 |
rs564583443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099215 | CCACTGCACTACAGC[C/T]TGGGTGACAGAGCAA | 10277 |
rs564623709 | snp | A/G | 6.69781e-05 | 0.00578659 | intron-variant | UBE4B | GRCh38.p7 | 1:10179412 | CTTTGCTTTGTCCCC[A/G]CAGACCCTCTGATGG | 10277 |
rs564624773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091817 | ACTATGTTGGTCAGG[C/T]TGGTCTCTAACTCCT | 10277 |
rs564652781 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112663 | CCTCAGCCTCCCAAA[A/G]TGTAGAAATATTTCT | 10277 |
rs564662134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092615 | GGTGAATCACCTGAG[G/T]TCAGGAGTTCAAGAC | 10277 |
rs564662750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116597 | GTGAGTTAAACACCA[C/G]ATTTGTTATGTGGCC | 10277 |
rs564665531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050034 | TGGAGAAAAACTGAA[A/G]ATGGCAAATATGGGA | 10277 |
rs564683388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10142405 | CGGCCCAGCGCAGTG[A/G]CTCACGCCTGTAATC | 10277 |
rs564690556 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168621 | TAAGGTGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 10277 |
rs564704223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053819 | CTCAGCCTTCTAAGT[A/G]TCTGTGACCACAGGT | 10277 |
rs564713816 | snp | C/G/T | 0.00438524 | 0.0466503 | intron-variant | UBE4B | GRCh38.p7 | 1:10090233 | CAGGTGACCCACCCC[C/G/T]CTCAGCTTCCTGAGT | 10277 |
rs564727600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173559 | CGACTATATAATACT[A/G]CACTGATTTAGAAAC | 10277 |
rs564774724 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10090987 | TCTGATCTTCCCACA[A/T]AGAATGCATAATTTC | 10277 |
rs564784627 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE4B | GRCh38.p7 | 1:10175426 | GGAGGCCAAGGCGGG[C/T]GGATCACAAGGTCAG | 10277 |
rs564827234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149393 | AAATTTGATGTAACT[A/G]TTTTAACTGAATGCT | 10277 |
rs564845719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098518 | GTAGACTATGAACTA[C/G]AGTGACGTGTCACTT | 10277 |
rs564848544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10152952 | CTAGGACCCAGTCCT[C/T]TGTGGAAGGCCCTTG | 10277 |
rs564889714 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10046813 | TTCAACCCTACTTAG[A/C]CCCAAATTACCAGAC | 10277 |
rs564925692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039958 | ACACCAAAAATACCA[A/G]GGACTGTGATTAACC | 10277 |
rs564927044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111889 | TTGAATCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10277 |
rs564935007 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150621 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGTGGGC | 10277 |
rs565002711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10113558 | CATGTGTGAGTGCAC[A/G]GTTTGTGAAAATATT | 10277 |
rs565009518 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10148641 | TGTCTCAAAAAAAAA[A/T]AAAAAATCAAGAAAA | 10277 |
rs565023767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10135588 | CTAAAAATACAAAAA[C/T]TAGCGGGTGTGGTGG | 10277 |
rs565074125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10061782 | TTTGGGCTACTCTCA[A/G]ACTTTTTCCTTTGAA | 10277 |
rs565108618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10164559 | TCTATAGCACATTCT[C/T]GTATTCATAGTCAGT | 10277 |
rs565120518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10112895 | TATTATAATTTTGAA[A/T]CACATTGACAAATAC | 10277 |
rs565154754 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10121333 | ATACTCCAGCCTGGG[C/T]AACAGAGCGAGACTC | 10277 |
rs565164016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154891 | ATACCAAAATAGTAA[A/C]AGCGCATTGGTTATT | 10277 |
rs565175814 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034270 | GGTACTTAATAGACC[A/G]CTAATGACTTCTGGC | 10277 |
rs565222424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10157370 | CAGTCCCAGCTACTT[A/G]GGATGCTGAGGTGGG | 10277 |
rs565222765 | in-del | -/AAAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042657 | GTCTCAAAAGCAAAG[-/AAAC]AAACAAACAAACATG | 10277 |
rs565223435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148554 | CAAGAATTGCTTGAA[C/T]CCAGGAGGCAGAGGT | 10277 |
rs565226470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10053428 | TCCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 10277 |
rs565227418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155463 | AAGTGGCAGCAACCT[C/T]GCAGATGCCCTTTAG | 10277 |
rs565245961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062610 | AGCCGCTGTACCGGC[C/T]GCCTTAATGCATTTT | 10277 |
rs565252077 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10070340 | AACTATGAAGAAGAA[G/T]AAGATGAATACCCAT | 10277 |
rs565261261 | in-del | -/A | 0.292266 | 0.246401 | intron-variant | UBE4B | GRCh38.p7 | 1:10148632 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs565275202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114289 | TCATCCTTGCAAAGT[C/G]CAGTGAATATAGTCA | 10277 |
rs565277946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055736 | ACCAGCCTGGTCAAC[A/C]TGGTGAAACCCTGTC | 10277 |
rs565283106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055177 | CTTTTGGCTTGAAAT[A/G]TTATGATTAGAATGG | 10277 |
rs565298285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10085368 | CTCTTGACTTCAGGC[A/G]GTTCTGTTTAATCAA | 10277 |
rs565309784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107257 | CCTTCCTCTTCCTCG[C/T]ACTTTCTGGGGACAG | 10277 |
rs565344782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100240 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 10277 |
rs565384552 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118600 | ACCTCTGCCTCCTGG[C/G]TTCAAGTGATTCTCC | 10277 |
rs565437668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076251 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 10277 |
rs565438628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076871 | CCTACCTCAGCCTCC[C/T]GATTAGCTGGGATTA | 10277 |
rs565438874 | in-del | -/CAC | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10123386 | AGTGAGCCGAGATTA[-/CAC]CACTGCATTCCAGCC | 10277 |
rs565446952 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100834 | GCTGGGATTACAGGC[G/T]TGAGCCACTGCACTC | 10277 |
rs565500821 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040720 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10277 |
rs565513759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170961 | TTATCAGATCAGAAA[C/T]GGGGAGTAAAGTTGA | 10277 |
rs565567142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175617 | GATCGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 10277 |
rs565572941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171551 | AGACTGCAGTGAGCC[A/G]TGATTGCACCACCAC | 10277 |
rs565575007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10068967 | TTCTCCTACTCCTTC[C/T]GTCATGTATGGACCT | 10277 |
rs565607108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091097 | ATAGCTTTCTCCATT[C/G]TGTGTTACACACCTC | 10277 |
rs565612245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069739 | AGGGTTTTGCCGTGT[G/T]GGCCAGGCTGGTCTC | 10277 |
rs565641307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083838 | TCGGGCCCCCAAAGG[G/T]GTATGTTTTATTAGT | 10277 |
rs565658596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128609 | CTAATATGCAGCCAC[A/G]TTTGTGAACTCCTGC | 10277 |
rs565670845 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142642 | CGCCACTGCACTCCA[A/G]CCTGGGAGACAGAGC | 10277 |
rs565697989 | in-del | -/AAAAAG | 0.007968 | 0.062614 | intron-variant | UBE4B | GRCh38.p7 | 1:10125134 | GTGTCTGGAAAAAAG[-/AAAAAG]AAAAAGAAAAAGATT | 10277 |
rs565700027 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032817 | CCCCTCCCCACGTCC[A/G]GCGCGGCTGCGCGGG | 10277 |
rs565706248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169905 | CTGTAATCCCAGCTA[C/T]TTGGGAAGCTGTGGC | 10277 |
rs565709778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075621 | GATTATGTTTCTCAC[A/G]TAGTCATCATTATTC | 10277 |
rs565747137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046224 | CTTGCTGGGAAGGCT[A/G]AGAAATAGTTTTTCT | 10277 |
rs565749384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144349 | AAAAATAAGGGAACA[A/G]TGTACTTTCTTGCAA | 10277 |
rs565785454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163238 | GCTTGGCTAATTAAA[A/C]AAATTTTTTTTATAG | 10277 |
rs565832512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142127 | CCAGGGATCATGTAT[A/G]TAGCTGTTTTTCTAC | 10277 |
rs565859390 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10097639 | ACATGTTGAAACCCC[A/C/G]TATCTACTAAAAATA | 10277 |
rs565863201 | snp | A/G | 4.9423e-05 | 0.00497082 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137189 | CGCAGACTCCGGGCT[A/G]TCCGGGAGCTCAATA | 10277 |
rs565889668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039008 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 10277 |
rs565910948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047972 | ATCCTTCTGCCTTAG[A/T]CTCCTGAGTAACTGG | 10277 |
rs565911528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10113894 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10277 |
rs565915608 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087014 | ATGCTAAAAGTGGAC[A/C]AGACCAGAGCAGATG | 10277 |
rs565946785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114513 | ATCAAGCCAGTCAGC[A/T]GATACCAGATCCTGC | 10277 |
rs565960920 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080416 | GTGAGAATCCATCTC[-/A]AAAAAAAAAAAAAGA | 10277 |
rs565971135 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089753 | CTTCCATCCTGGAGG[G/T]CAGTGGCTCAATCTC | 10277 |
rs565985399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107353 | GTGGTGATGATTTTT[A/C]TTGTGTCCAGTTTGG | 10277 |
rs565990882 | snp | C/T | 9.87606e-05 | 0.00702642 | intron-variant | UBE4B | GRCh38.p7 | 1:10135208 | ACTGTGTTCGTGACT[C/T]GGTCATTAAAACACT | 10277 |
rs566025771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039385 | GTGTGTGGCAGGTAC[C/G]TGATCTTGGAGGGCT | 10277 |
rs566050252 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10156382 | GTAGCTGGGACTGCA[A/G]GCATGTGCCACCACA | 10277 |
rs566055201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176823 | TGGAGTCTCCCTCTG[C/T]TGCCCAGGCTGGAGT | 10277 |
rs566117231 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10057744 | CACAGAAAAAAAAAA[A/G]AAAGAAAGAAAAAAG | 10277 |
rs566131772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093625 | GGAAGGGTTAAAATT[A/G]TATTTATTCAGTGAT | 10277 |
rs566183585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10086206 | TCGATCTCCTGACCT[C/T]GTGATCTATCTGCCT | 10277 |
rs566184531 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054043 | TTTTTTTGTTGTTGG[C/G]GTAGTAATTAGAAAT | 10277 |
rs566192856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10130129 | CCCAGGCTGGAGCGC[A/G]GTGGCGCAATCTCAG | 10277 |
rs566213464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10041965 | CTCCCAAAGTTGTGG[G/T]ATTACAGGCATGATG | 10277 |
rs566216345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147300 | GAGTTCAAGACCAGC[C/T]TGGCCAACATGGCGA | 10277 |
rs566216465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10139810 | CTTGGCTCACCTCAA[C/T]CTCTGCCTCCCAGGT | 10277 |
rs566237861 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10062144 | CGATTTCTTGACCTC[A/G]TGATCCACCCACCTC | 10277 |
rs566244253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163703 | AAGAGAGAGAGTCTT[G/T]CTAGTTTTCCCAAGC | 10277 |
rs566245399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174594 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10277 |
rs566310939 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100102 | TCAGGCCATTCTCCC[G/T]CCTCGGCCTCCTGAG | 10277 |
rs566316119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100008 | ATTTTTTATTTTTTT[A/G]AGATGGAGTCTCGCT | 10277 |
rs566345143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117932 | TATAATAACCAACAT[C/T]ATAGAGCCTCTGTAG | 10277 |
rs566371741 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102128 | CAAAGGAAAAAATAA[G/T]AAGTTGCACTGTAGC | 10277 |
rs566396292 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131407 | CAAGGATCACTTGAA[C/T]CCAGGAGGTGGAGGT | 10277 |
rs566397194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071198 | GCGTGAGCCACCACA[C/T]CTGGCCAATTGGCTA | 10277 |
rs566411665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055325 | TTCTTTTCTTTCCTT[C/T]CTTTATTCTGAGACA | 10277 |
rs566446132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081165 | CCTCCTGGGTTCAAA[C/T]GATTCTCCTGCCTCA | 10277 |
rs566479039 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175960 | ATGTATCACCCCAAA[A/G]GGAAAACCCTTAAAG | 10277 |
rs566486807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044314 | CTTGCCTCGGCCTCC[C/T]AAAGTGCTAGGATTA | 10277 |
rs566488137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059647 | TGGCTGCTTAGGGCA[A/T]GGCCGAGGCGTGAAG | 10277 |
rs566504393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095732 | AATTAGTGTCAAATG[G/T]ATTAAATTTAAAGAT | 10277 |
rs566514961 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038926 | TTTGCTGGGTGTGAT[G/T]GTACGCACCTGTAAT | 10277 |
rs566516330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159363 | CTGAACTCTTGAATT[A/C]TTCTTCAAAAATTTT | 10277 |
rs566536324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096442 | AAACAGATGAAGAGG[A/G]GAATTAAGTCCGGGC | 10277 |
rs566536493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088441 | GCTGGCGTGCAGTGG[C/T]GCAATCTCACTGCAA | 10277 |
rs566561879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10109942 | GACCTCAGGTGGTCC[A/G]CCCACCTCGGCCTCC | 10277 |
rs566572895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088979 | CCACCACACCCAGCC[C/T]ACTTTATTTTTGTTT | 10277 |
rs566631205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064857 | CAGCCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 10277 |
rs566631701 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10152706 | AGGAGGCCGAGGCAC[A/G]AGAATCGAGTGAACC | 10277 |
rs566698421 | in-del | -/TTTTCTTTTTTCT | 0.0107246 | 0.0724382 | intron-variant | UBE4B | GRCh38.p7 | 1:10068338 | CCTGGCACAGTTTTC[-/TTTTCTTTTTTCT]TTTTCTTTTTTTTTT | 10277 |
rs566702981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038003 | TAGAAAGTGTTGGCC[A/G]GGCGCAGTGGCCCAC | 10277 |
rs566737826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10160053 | ATGGGCTTACCACCC[C/T]GTAGTTGCACAGTTG | 10277 |
rs566751597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175305 | CATGAAGCATTGTCT[C/G]TTAACACCATTTTCC | 10277 |
rs566771138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10057684 | GCAGTGAGTTGAAAT[C/T]GTGTTACTGTACTCC | 10277 |
rs566772927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10065340 | TATGGGGCAAGTGGC[A/G]GGAGGAGCATGCGGG | 10277 |
rs566777095 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178588 | ATATTTTCTGCAGCT[C/T]GCTTTTTTCCACCTG | 10277 |
rs566792250 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079208 | TTGAGATGGAGTCCC[A/G]CTCTGTCGCCCAGGC | 10277 |
rs566809654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10058563 | AGCTGGGCATGGGGT[A/G]CAGAGCTGGGGGAGT | 10277 |
rs566827579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10168867 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGTGAGA | 10277 |
rs566875860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141091 | ATCAAGCATCCTCAG[A/C]ATCCATTCCCATACA | 10277 |
rs566937060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10154483 | TTCAATGGAAATAAT[C/T]ACGAATGTTTGTAAG | 10277 |
rs566940001 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138006 | GTGGTACGATCTCAG[C/T]TCGGTGCAACCTCTG | 10277 |
rs566940104 | in-del | -/G | 0.0013058 | 0.0255186 | frameshift-variant, intron-variant | UBE4B | GRCh38.p7 | 1:10106541 | CACCCGCCTCACCCA[-/G]TGCCACGAGCAGACG | 10277 |
rs566941581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141708 | GGAAGCGAAGAGGGA[A/T]GATGGGTTAGAACCT | 10277 |
rs566956096 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105313 | ATATCTTATATAACC[A/G]TGGTACATTTGTCAA | 10277 |
rs566988516 | in-del | -/AAC | 0.0267683 | 0.11255 | intron-variant | UBE4B | GRCh38.p7 | 1:10073724 | TTCTGTCTCAAAAAC[-/AAC]AACAACAACAACAAC | 10277 |
rs567011469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148203 | CTGCACTCCAGCCTG[A/G]GTGACGAGCAAGACT | 10277 |
rs567051365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10134436 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 10277 |
rs567055942 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10126554 | TGGGGGTCCTGTCAG[A/T]GTATTAGAGTTCACC | 10277 |
rs567128451 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090782 | ACGGTGGAATTTAGA[A/C]GCCTATGCATTTGTG | 10277 |
rs567131372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10074541 | TCTTTGCTGAATCAA[C/T]TGCAGTCAGGCGAGG | 10277 |
rs567158722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111432 | AGCTGTATGGCCGGC[A/T]CCCTCACTCTCCTCA | 10277 |
rs567160653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103325 | ATACTATGTAAATAG[A/G]TTAATGGTCTCCATT | 10277 |
rs567211551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175373 | ATAAAAAAAAATAGC[C/T]GGGTGCAGTGGCTCA | 10277 |
rs567249457 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124222 | GCTGGAGTGCAGTGG[C/T]GCCGTCTCAGCTCAC | 10277 |
rs567295259 | snp | A/G | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126813 | TTATCCCCATTTTAC[A/G]AGGCCTGGCTCTTGC | 10277 |
rs567300829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089053 | GCTCTATGGCCCAGG[A/C]TGGAGTGCAGTGGCG | 10277 |
rs567300942 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093413 | TCAGAATTCTCACTA[C/T]GGTAGATGCTTTGTG | 10277 |
rs567320906 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180404 | CCTGACCCTACTTGC[A/G]CTGCTGTGGATTTTT | 10277 |
rs567334850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10121549 | CAGGCACACACCATC[C/T]TGCCCAGTTGATATT | 10277 |
rs567336742 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10148024 | CATGGTCAGGAGATC[A/G/T]AGACCATCTTTGCTA | 10277 |
rs567350967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081848 | CCCGCTTCGGCCTCC[C/T]AAAGTGCTGGGATTG | 10277 |
rs567379235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10175448 | CAAGGTCAGGAGATC[A/G]AGACCGTCCTGGCTA | 10277 |
rs567386722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10154357 | CGGGAGGTGGAGGTT[A/G]TAGTTAGCCGAGATC | 10277 |
rs567417027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053532 | CAATCAAGTTCTGGG[A/G]TATATGGGCTGGATG | 10277 |
rs567432564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160843 | AGCTACTTAGGAGGC[C/T]GAGGCAGGAAGATTG | 10277 |
rs567446672 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168376 | AATTTTAGGATCACA[C/G]TCATCAATAAGTGAA | 10277 |
rs567455544 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10046345 | ACAACCCCGGATCAA[C/T]TTCAGAGTCCAGAAT | 10277 |
rs567483125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043875 | AGTGTTAAAATTAGT[C/T]GCCATTTTAAATGCC | 10277 |
rs567507479 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031271 | ATTTTTGTATTTTGT[A/G]TTTCACCATCTTGGC | 10277 |
rs567532273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153822 | GGCACAGTGGCTCAC[A/G]CTGTAATCCCAGCAC | 10277 |
rs567535140 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10096121 | ATGGTGTAGTCAGTT[-/A]AAAAAAAATCTATTG | 10277 |
rs567563181 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE4B | GRCh38.p7 | 1:10130911 | GCCCAGTAGACAAAC[A/G]GCTAACAAAAGCCAA | 10277 |
rs567563416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10051343 | TGTAGTGACCTGGCC[G/T]AGTGGATTCTTGGGA | 10277 |
rs567563457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10059422 | ATTCCCCAGATCCAG[A/G]AGGGGAAACAGGTGT | 10277 |
rs567597774 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10052015 | CATTCAATGCATATT[G/T]CTTCTTTGTTCCCTG | 10277 |
rs567621442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162166 | ACCACACCTGGCTAG[G/T]TTTTGTATTTTGTTT | 10277 |
rs567629425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154522 | TCCACAGCATTATTT[A/G]TAAAGCAGTGCAGTG | 10277 |
rs567642632 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150975 | GACCATCCTGGCTAA[C/T]ATGGTGAAACCCCAT | 10277 |
rs567643049 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032392 | AAATAAAATGAATGG[G/T]AGTTCTTGTGTTCGA | 10277 |
rs567695589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10149593 | TAAATGTCTGAATGA[A/G]CATCCCAAAACCAGA | 10277 |
rs567699977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10105861 | GGTATGGCATATATC[A/G]TATTTGGGGAGGTGG | 10277 |
rs567714325 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161193 | GATAAACGACACGAC[A/G]TTTTTGCTCGATGAA | 10277 |
rs567725098 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163542 | GTGTGGTGGCACGCC[A/G]CTGTAGTCCCAGCTA | 10277 |
rs567725265 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10138268 | ACACCCAGCTAATTT[G/T]TTGTATTTTTAGTAG | 10277 |
rs567727583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148804 | AATTAGCCAGGTATG[A/G]TGGCACGTGCCTGTA | 10277 |
rs567744011 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158277 | GTTTACATTCACTCA[A/G]TATCATTGTTGGGGC | 10277 |
rs567756331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10091187 | GGGTTACAGCAGATT[A/G]TGTTCATTTTTTAAT | 10277 |
rs567789393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142492 | CCTGGCCAACATGGT[A/G]AAACCTCGTCACTAC | 10277 |
rs567811342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056639 | AAATATTTTGTCACT[G/T]TCTTATAAATGGGGA | 10277 |
rs567822797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120296 | GAGGCTGAGGCTGGC[A/G]GATCACCTGAGGTCA | 10277 |
rs567832224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10127618 | TAGTTTATTCTATGT[A/G]TAAATTAAGTCTTAT | 10277 |
rs567848005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049295 | CCTCAGGCTGCAGCT[A/G]GGGACACAGGAACGC | 10277 |
rs567869127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10119275 | ACCGCGCCTGGCCTC[C/T]AAGGTTCTTAAGTAT | 10277 |
rs567885485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169042 | AAGGTTAATGGGAGC[C/T]GGCCATCACTAGGGT | 10277 |
rs567896992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034832 | ATGATTTTGTTGATT[A/G]TGATACTTGGATACT | 10277 |
rs567916459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10112167 | AAGGATGCAGCTCTG[C/T]TTCTATTATGTGAAG | 10277 |
rs567942148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066881 | ACCGCACTCCAACCT[A/G]GGTGACAGAGCAAGA | 10277 |
rs567970118 | in-del | -/ATG | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10167472 | ATAATAATAATAATA[-/ATG]ATGACTAAGTAAAAG | 10277 |
rs568002791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165102 | CTCCAGAATATATCT[C/T]CCTGGCTCAGATCTG | 10277 |
rs568015274 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10157731 | GCAGTGAGCTGAGAT[C/G]GTGCTACTGCACTCC | 10277 |
rs568015310 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10165744 | TCCTTCAGATATACC[C/T]TCCCTCAGGGATACC | 10277 |
rs568037430 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10044457 | AGACACTTTTTCCAT[-/G]GGTGGTGGTGGTGGG | 10277 |
rs568058642 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134404 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 10277 |
rs568060308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108230 | TTCACCCCCATTGAG[C/T]TCAGTCTGGGCAATC | 10277 |
rs568105599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145251 | GAATATGGATAGATA[C/T]GCTTCTGCTGTGATT | 10277 |
rs568150403 | snp | A/T | 1.64732e-05 | 0.0028699 | intron-variant | UBE4B | GRCh38.p7 | 1:10130670 | TTCAGATTCTTTCCC[A/T]AATGTGCATTATATG | 10277 |
rs568157474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102436 | TTTTTTTTGAGACAG[A/G]GCCTCACTCTGTTGC | 10277 |
rs568159022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080659 | TATGGAAGCAACCTA[A/G]ATAATCCATCTTCAG | 10277 |
rs568189676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172604 | TATCCAAATACTATT[C/T]ATGGCTCAAGTTAAT | 10277 |
rs568191893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152240 | TTCCAGCCTGGGCAA[A/G]AGAACAAGACTCCGT | 10277 |
rs568226223 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074190 | ATCACATCCATCTGC[C/T]TACCTGTATGTGCGC | 10277 |
rs568244549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070848 | CTCCTACAAGTGATG[A/G]TTAAATTTGTGTCTT | 10277 |
rs568288652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050109 | ACAGAGTCTTGCTCT[G/T]GTCACCCAGGCTGGA | 10277 |
rs568296261 | in-del | -/ATTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103447 | TTTATTTATTTATTT[-/ATTT]TGAGATGGAATCTCA | 10277 |
rs568306840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123943 | CACACCCAGCTAATT[G/T]TTTGTATTTTTATTA | 10277 |
rs568324746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115603 | TCCAAGGTCAATTAT[A/G]TGTAGTTTTCCAAAG | 10277 |
rs568348320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125082 | ATTTAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 10277 |
rs568359924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10071488 | AGATACTTAGGAGGC[C/T]GAGGTGGGAAGATTA | 10277 |
rs568360706 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116811 | TCTAGCTTCAGGTAA[C/T]AAGTAAGCAGTGGGG | 10277 |
rs568360799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086964 | GGCTTGAGCCACCGC[A/G]CCTGGCCTCCCCGTC | 10277 |
rs568375711 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093692 | TTTCTTTTTTCATAC[-/T]TTTTTTTTTCTTTTT | 10277 |
rs568384953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117301 | TTGTTGGCTTTGGAG[C/T]AGGTGAAACAAGCAG | 10277 |
rs568406587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072829 | CTTTTCTATCAAATA[C/T]AGTATTATTGTCATA | 10277 |
rs568419807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079969 | CTCAGGGGCCTCCAG[A/G]GGCTCACTGTTTAGC | 10277 |
rs568444797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064909 | GCTGGGGTTACAGGT[C/G]CCCGCTGCCATGCCC | 10277 |
rs568464084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125944 | TTTAATGTAGTAATA[A/G]TGTTGATTGTTGGCC | 10277 |
rs568466162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174433 | GGGCTGGGTGCGGTG[G/T]CTCACACCTGTAATC | 10277 |
rs568480453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049563 | CAGCCTGGGCAATAT[C/G]ATAAGACCTTTTCTC | 10277 |
rs568483209 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10037519 | TTCTATAATCTACTC[-/AT]GTGTTGTTTTTCGTA | 10277 |
rs568484168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152408 | ATCTACCCTATAGCC[A/G]GTGTGCAGATTTAGT | 10277 |
rs568493297 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | UBE4B | GRCh38.p7 | 1:10166968 | ACACACACACACACA[A/C]ACAAAAAAAAAAAAT | 10277 |
rs568502686 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086704 | CCTCTCTCTTTTCTC[-/T]TTTTTTTTTTGAGAT | 10277 |
rs568518560 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10050418 | TAGCCAAATGTGTGA[A/C]CCCAAGCTCTCCAAA | 10277 |
rs568521257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073655 | AACCCGGGAGGTGGA[A/G]GTTGCAATGAGCCAA | 10277 |
rs568560098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065360 | GAGCATGCGGGGGAG[C/G]AAGGCACAGCTCCAC | 10277 |
rs568572895 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10035725 | ATAGTTTTTTTATTT[A/T]TTTTTATTTTTTATT | 10277 |
rs568590885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10145693 | CACCCCTCGCCCCAA[C/T]ACTCATCCAGTATAT | 10277 |
rs568591961 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053547 | GTATATGGGCTGGAT[A/G/T]TGTAAGTTTGTTACA | 10277 |
rs568594836 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177064 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCG | 10277 |
rs568609467 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10084365 | GGCTTGCAAGGTGCT[C/G]TATCATCATGTTCCA | 10277 |
rs568610982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10178297 | AGACTAGATTTCCTT[C/T]TCTTTTTAATGTTTA | 10277 |
rs568623772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10138376 | TGCTGGAATTACAGG[C/T]GTGAGCCCATGCACC | 10277 |
rs568653222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043411 | TAATATCTTTGAAAT[A/T]GAGATGCTGCTTTTT | 10277 |
rs568666030 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094656 | AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACCTTGT | 10277 |
rs568685744 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE4B | GRCh38.p7 | 1:10042221 | GCATTTTCTCACACG[A/G]CACTTGTAGTATCTA | 10277 |
rs568692455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124082 | ACCTGGCCTCAAGCC[A/G]TCATTTTGAAGTGTA | 10277 |
rs568779352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036649 | TCTTTGAAGTTTTTC[C/T]TTTTAATTCAATTAA | 10277 |
rs568797266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132060 | GCTTGAACCTGGGAG[A/G]CGCAGGTTGCAGTGA | 10277 |
rs568801731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10057534 | CGCTTCTCCTGCCTG[A/G]GCCTCCTGAGTAGGC | 10277 |
rs568811033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10158779 | TTTGGGAGGCAGAGG[C/T]GGGCGGATCACTTGA | 10277 |
rs568820848 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10099171 | TGCTTGAACCTGGGA[A/G/T]GCAGGGGTTGCAGTG | 10277 |
rs568830585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10109800 | GGATTACAGGTGCAT[G/T]CCACCACACCTGGCT | 10277 |
rs568841103 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10145766 | GTAGTGGAAAGATCT[C/G]TTTCCTTTGCCCCTC | 10277 |
rs568869738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087605 | ATGATAAGACTGGGG[A/T]TGTGGGTTTTGGGGA | 10277 |
rs568903809 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038398 | ATTGACATTAAACAA[C/T]AGCCTTAGGAGCCTC | 10277 |
rs568904161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102593 | TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTTCA | 10277 |
rs568906410 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10139046 | GCCTGACCTGTAATT[G/T]TCATTTCTTGTTAAG | 10277 |
rs568929990 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10065424 | AAGGAAGAGGAGACC[A/G]CTGTACTTCACTGTA | 10277 |
rs568946831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094670 | CAATCTCCTGACCTT[A/G]TGATTCACCCGCCTC | 10277 |
rs568974897 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095041 | GCCTTGGCCTCCCAA[A/C]GTGCTGGGATTCCAG | 10277 |
rs568993414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165875 | GTTTCTATGAAGCAG[A/T]TCCTCCCTAACGGAA | 10277 |
rs569026028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124924 | TGAGCTCAGGAGTTC[A/G]AGACCAGGCTGGGCA | 10277 |
rs569032486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071658 | AACAGAGATGGTAAG[A/G]GAACTAACATACAGT | 10277 |
rs569048393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064188 | GTCTGCCTAACCCCT[A/G]CCTGTCCTGAAAAAG | 10277 |
rs569076831 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096593 | TGGGCCTGGTGGCAG[C/G]CGCCTGTAATCTCAG | 10277 |
rs569088129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043727 | TCCAACGCGCTGGGC[C/T]GGGATGCTTCTTATA | 10277 |
rs569091955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178541 | TAGGGCTTTTTTAGT[A/G]GGGGAAAATCCACAA | 10277 |
rs569138504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118219 | CTGATTTTAATTTTA[C/T]GTTAGAAACGAACCT | 10277 |
rs569175050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10144191 | AGGAGCAAAGCCAGA[A/G]ATAACCTCAGAGAAG | 10277 |
rs569175063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10111224 | ATACTACACACACAC[A/G]CACCACGCGCTACAC | 10277 |
rs569190868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160301 | GTGATAAGGAATAAC[C/T]ATATCAGTTGTTTTC | 10277 |
rs569201111 | snp | G/T | | | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106463 | CTGCCCTCGCCAGTA[G/T]CCCCCAAGCAGTGCC | 10277 |
rs569232545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10073824 | CCCAGTTCACTCACT[C/G]TGCTGATCTGTTTCA | 10277 |
rs569242745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058839 | TTGGATGCCACTGAC[C/T]AGATGTGGCTCCCAG | 10277 |
rs569256316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126500 | CAACAGGCTCCAAAT[C/G]TATGGGTTTTGTTGA | 10277 |
rs569267354 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040763 | GCTGGGATTACAAGC[A/G]TGTACCACCATGCCT | 10277 |
rs569328494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036755 | TGAAAACTTGTGTCA[A/G]ATATGGTAGGTGACA | 10277 |
rs569345105 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158000 | TTTTTATCCGCTGAA[A/G]TATGTCCATTTGAGG | 10277 |
rs569355747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087100 | TCTGTTCTCGTCTGA[C/T]GCATACAGGTGTATC | 10277 |
rs569361224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059578 | AGCTTGAAGCCCATT[G/T]AGCTCATGCAGTTCC | 10277 |
rs569385997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153997 | TGAGGCAGGAGAATC[A/T]CTTGAACCCGCGAGG | 10277 |
rs569389924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139747 | TTGAGAGGAGGTTCA[C/T]TCTTGTTGCCCAGGC | 10277 |
rs569399670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080071 | TCACTTTCTCAGGCT[C/T]CCGGCTATGCATTGT | 10277 |
rs569407189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069838 | AGATGTGCAGTGTAC[A/G]GATGTCCATTGTGCA | 10277 |
rs569433110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132225 | TGTGGATATTTCTTA[C/T]ATTCTTTCACTCAGG | 10277 |
rs569470405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10167395 | GGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 10277 |
rs569479830 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155427 | AAGGGTCAAGAAGCT[C/T]GCTGAAGGTCAGTGG | 10277 |
rs569484754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046898 | TTCATCTTTGCATGC[A/G]AATTGGCAAGCTTTG | 10277 |
rs569492289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10132887 | TTTGGTACAAGCCCA[C/G]CACGCAGGCTTTTGT | 10277 |
rs569527731 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097916 | CACTCTGTCTCCCAT[A/G]CTGGAATGCCGTGGC | 10277 |
rs569561362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10084068 | CCTGCAACCTCTGCT[A/G]TGCTTGTAGTTTTAC | 10277 |
rs569565221 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040909 | ACCGGCGTGAGCCAC[C/T]GCACCCAGCCTAACA | 10277 |
rs569587274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10171938 | AAAGAGCAGGTTTGG[C/T]GCTCTGAGCCCTCTC | 10277 |
rs569614027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10126013 | TTTTAAAAAATATTG[A/G]TAGAGGGCCAAGCGC | 10277 |
rs569635723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076533 | ACACACGTGAGCTAC[C/T]ACGCCTGGCCAAGAA | 10277 |
rs569651529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10121341 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCTA | 10277 |
rs569656168 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10145501 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATGGC | 10277 |
rs569660393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10130000 | AAACTAACAAGAGGT[A/G]TGGAAAAGTTATTCG | 10277 |
rs569671932 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE4B | GRCh38.p7 | 1:10069960 | ATCAAGCATGAACTC[C/T]TAAATTTAGCTGTCT | 10277 |
rs569704717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163250 | AAAAAAATTTTTTTT[A/G]TAGAGACAAAGTCTC | 10277 |
rs569705203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142927 | CGCCTGGCCAACATG[G/T]TGAAACCCTTTTCTA | 10277 |
rs569723992 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173792 | CTGCCACATCACAGG[C/T]GCTTAACGTAACACA | 10277 |
rs569724556 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10062222 | CCTATTTTTTCTACC[A/G]TCATTTTGCTTGTGT | 10277 |
rs569762162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10040319 | TTCACCATATTGGCC[A/G]GGCTGGTCTTGAACT | 10277 |
rs569804546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039537 | CGGGTTCAAGTGATT[A/C]TCCTGCCTCAGCCTC | 10277 |
rs569809779 | snp | C/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031154 | GGAGTGCAGTGGCAC[C/G]ATCTCGGCTCCTTGC | 10277 |
rs569845950 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10131442 | GTGAGCCAAGATCAC[A/G]CCACTGCACATCAGC | 10277 |
rs569862386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10164560 | CTATAGCACATTCTC[A/G]TATTCATAGTCAGTA | 10277 |
rs569876806 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166410 | AAATTTTAAAAGCTT[A/T]GTAGTCCACAGGCAC | 10277 |
rs569884885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10135796 | TATCATAATATATCT[A/G]TAAAAAAGCCAAAAC | 10277 |
rs569908417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137341 | TCTGTCTGCCTCCAC[C/T]GCCACATCCATGTTG | 10277 |
rs569948769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108185 | TGCGTGCTCCCTTCC[C/T]ACCCCCTCCCAGCCT | 10277 |
rs569949105 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061862 | ACTTACTGTGTTGCT[A/G]TACGTGTGTAGTGTG | 10277 |
rs569965731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10034944 | AATATTACACAGTTT[C/G]TTTCATTCGGTAGGA | 10277 |
rs569984627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100893 | CCCAAGAAAATGACA[A/G]CTTAGGAAAAATATT | 10277 |
rs570075831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070683 | TGGAGATGCCCTGCT[A/G]TTAGTAGGAGTTCAA | 10277 |
rs570091487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172824 | ATGTGCTGTTTCTGT[C/T]GATGCTGGACCACAA | 10277 |
rs570111322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10179195 | CTTTCTTCTCTGTTC[C/T]CTCCCCCCAGCAGTA | 10277 |
rs570116333 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104630 | TTTACTTATTAACTC[C/T]GCTAATGGAGCAGAC | 10277 |
rs570123500 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158926 | GAGGCAGGAGAATCA[C/G]TTGAACCCGGGAGGC | 10277 |
rs570124146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177485 | ACAAAGCGAGACTCC[A/G]TCTCAAAAATTAAAA | 10277 |
rs570179017 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE4B | GRCh38.p7 | 1:10035506 | GGTTCACGCCATTCT[C/T]CTGCCTCAGACTCCG | 10277 |
rs570184702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070971 | GGCTAGAGTGCAGTG[G/T]TGCCATCTCAGCTCA | 10277 |
rs570231555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055366 | GTTTCCCAGGCTGGA[G/T]TGCACTGGCAGCATC | 10277 |
rs570236211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10055851 | CTTGAAGCTGGGGAT[A/G]GAGGTTGCAGTGAGC | 10277 |
rs570273519 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093071 | CTATATTGCTACAGT[A/G]TTATTGTACACATAC | 10277 |
rs570286782 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090348 | TGGTCTTGAATTCCT[A/G]GACTGAAGCGATCTA | 10277 |
rs570290846 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071608 | GTGTAATATGCTTAC[C/T]GTAAATTCGCCATGT | 10277 |
rs570313233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143754 | GGGAACTAGTTGGTT[C/T]ACTGAATCATTGGAA | 10277 |
rs570348014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150979 | ATCCTGGCTAACATG[A/G]TGAAACCCCATCTCT | 10277 |
rs570355226 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074070 | CAGTCTCTCATGTAG[C/G]TGGGACTATAGGCAT | 10277 |
rs570361621 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102940 | CTGCAAATCTTCTTC[C/T]TCACCAGGAGCCTTC | 10277 |
rs570377875 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102275 | TCCTGGAGGAAAATT[G/T]GTCATGCACCTGGAG | 10277 |
rs570386728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164876 | CTAGTGGAATTTGGT[A/G]TAATAATAACTCATG | 10277 |
rs570403870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10114796 | TTGAACCCAGAAGGC[A/G]GAGTTTGCACTGAGC | 10277 |
rs570406572 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044045 | GTTTCTTTTCTTTTC[-/T]TTTTTTTTTTGGAGA | 10277 |
rs570406886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10108206 | CTCCCAGCCTCCACC[C/G]CCCCCCTGTTCACCC | 10277 |
rs570426967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069911 | CTCCAGATAAGTAAA[A/G]TAGTCAGTAATAAAG | 10277 |
rs570433423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172513 | GAACCCATATCCTCA[A/G]TCTCTCTGCTGTCCA | 10277 |
rs570440554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123247 | ACCAGCCTGGCCAGC[A/G]TGGTGAAACCCGGTC | 10277 |
rs570442507 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBE4B | GRCh38.p7 | 1:10045786 | GGTCAAACACTAGAT[C/G]GTCAGATACATTTTG | 10277 |
rs570445911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107625 | TCTTGTTGCCCAGGC[C/G]GGAGTGCAATGGCGC | 10277 |
rs570449199 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084864 | ACCATTCCTGGCTAA[-/T]TTTTTTTTTTTGTAT | 10277 |
rs570451066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10157667 | TCTATAGTCCCAGCT[A/G]CTAGGGAGGCTGAGG | 10277 |
rs570571444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10151035 | GGGCATGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 10277 |
rs570572763 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10033903 | ATTCTGAACTCCATT[G/T]GCTTCTTTCCGAGTG | 10277 |
rs570651464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10124986 | CAAAAAATTAGCTGG[C/T]GCAGAAGTGCATGCC | 10277 |
rs570651618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10116285 | GTGGCTGGGATTACA[A/G]ACGTGTGCCACCACG | 10277 |
rs570665177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10076662 | GGGCTGTTTTCAGTT[G/T]CAAGTAACTAAAGCA | 10277 |
rs570729475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164250 | GAAGGCTGAGGTGGG[A/T]GAATCACTTGAACCC | 10277 |
rs570738258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093757 | TGCAGGGCAGTGGGG[C/T]GATCTTGGCTCACTG | 10277 |
rs570748028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077709 | CCAGCTGGATTGTCT[A/G]TTTTTCCTGATGTGC | 10277 |
rs570785380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138716 | TGAAATTTCCATCTT[C/G]TTTCAGTTGGTGGAG | 10277 |
rs570796814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079086 | AATCTCTCAAAGTAT[G/T]GGGATTACAGGCATG | 10277 |
rs570809620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086890 | ACACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10277 |
rs570833531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071741 | CACTGCTTTGCTCAG[G/T]CTGGTCTTGAACTCC | 10277 |
rs570854912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10178210 | ATGCTTACCTTTGTG[A/G]AAGAGAGCTGAAATT | 10277 |
rs570875526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036479 | AGAACAAATAATATT[C/T]GTTTGTTTTTAATTT | 10277 |
rs570889598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173508 | AATTATATATATATA[C/T]ACACACACACACACA | 10277 |
rs570899473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10079802 | GCTGCTAGTTTTTAA[A/C]CTACTTAATGATTAT | 10277 |
rs570914663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10127726 | ATGAATTCATTACTG[A/G]CGATCTGTTCTGTGC | 10277 |
rs570921318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048500 | TGAGCCTCCATCCAT[A/T]CCAGCAATTAAAGGT | 10277 |
rs570938085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10072644 | AACTTTTTCTTTAAC[C/T]TTTCAGAGGATAAAA | 10277 |
rs570945406 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159538 | ATTAGCCAGGCATGG[C/T]GGTGGGCGCGGTGGC | 10277 |
rs570948915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165989 | TACACATTTAGGTAG[A/T]TCACGCCTGGCTGTT | 10277 |
rs570950013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100969 | GAACTCTTAAAAATT[A/T]ATAAGAAAAAAGATG | 10277 |
rs570970496 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138517 | GAGATTACAGGTGTG[A/G]GCCACCGTGCCTGGC | 10277 |
rs570979486 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10047213 | TGACTGCTGTGGCAG[A/G]GGTCGGAAATAATAA | 10277 |
rs570979603 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082889 | GTTCAACTCCCATTT[A/T]TGAGTGAGAATGTGC | 10277 |
rs570987398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056592 | TGTTTGTTATATTAC[C/T]TTTATTTCTGATGAC | 10277 |
rs571054714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10101559 | TGTCGCCCAGGCTGG[A/T]GTGCAGTGGTGCGAT | 10277 |
rs571058798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042218 | AGTGCATTTTCTCAC[A/G]CGGCACTTGTAGTAT | 10277 |
rs571101209 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10103982 | GGCCAGGATGGTCTC[C/G]ATCTCTTGACCTCGT | 10277 |
rs571106430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10138243 | GCTGGGACTACAGGC[A/G]CCCACCACCACACCC | 10277 |
rs571112039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137441 | GATATTTCACTCTGT[A/T]TATGGTTACTACAGA | 10277 |
rs571136954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10096737 | AAAAAAAGAAAAAGG[A/G]GAATTAAAAATATGA | 10277 |
rs571143007 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10104611 | AGATAAGACTATTTC[C/T]GATTTTACTTATTAA | 10277 |
rs571144271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145101 | AATTTTCCCAACAGA[A/G]TATATGCCTTGAGTG | 10277 |
rs571151570 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102691 | GCTGGGATTACAGGT[A/G]TGAGCCACCACGCCC | 10277 |
rs571180099 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10097455 | ATTCCACATTTTTTT[A/C]TCTACTGGTTTGAAA | 10277 |
rs571180249 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062500 | GTATTTTTAGTAGAG[A/C]CGAGGTTTTGCCATT | 10277 |
rs571181375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134460 | GAGGTTGTAGTGAGC[A/G]AGGATCGTGCCACTG | 10277 |
rs571201762 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10042594 | AGGGGTTACAGTGAG[C/T]TGAGATTGCACCACT | 10277 |
rs571205097 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032013 | CTGCCTCAGCCTCCC[A/G]AGTAGCCGGGACTAC | 10277 |
rs571217459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127279 | TGAATACAATTTTAT[C/T]TTTATGTGTTTACTT | 10277 |
rs571234470 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171473 | GATTTGGGCTGGGCG[C/T]GGTGGCTCAGGCCTG | 10277 |
rs571235940 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031357 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 10277 |
rs571243862 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180528 | TGGGATCGTATTTTT[A/G]TATCATATTCACATA | 10277 |
rs571271532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10046505 | TGGGGAGTAATACTC[C/T]GCGCTGGTCCATAGC | 10277 |
rs571305839 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064789 | TTTTTTTTTAGATAG[A/G]GTCTCACTGTGTTGC | 10277 |
rs571320117 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10175509 | ACAAAAAATTAGCCA[G/T]GCGTGGTGGCGGGCG | 10277 |
rs571331768 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093805 | GTTAATGCGATTCTC[C/T]TGCCTGAACCTCCCA | 10277 |
rs571334117 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10125113 | CCTGTGCGACAGAGT[G/T]AAATTGTGTCTGGAA | 10277 |
rs571352177 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10075079 | TCTAGACCTGGATTG[G/T]CAAACTCTTTCTGTT | 10277 |
rs571358344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052697 | CATGGGGCCCTGAAC[A/G]TTCTGTAGCTGGTCT | 10277 |
rs571373810 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040401 | GGTGTCAGCTACCAC[A/G]CCAGGCCTCCGGCTA | 10277 |
rs571384719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052089 | TTTTTTTTTTTGAGA[C/T]GGGGTCTTGCTCTGT | 10277 |
rs571389329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075583 | TTAGTTCTTGCCCGG[A/G]TACCTCTATGCTAAG | 10277 |
rs571437800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10141245 | CTTTGCAGCTGTGAT[A/G]TCAGGTTCATGATCT | 10277 |
rs571455085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10143648 | CGAAGGATTCGGATG[C/T]GACAAGTTTGGAGGA | 10277 |
rs571467184 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10044538 | TCCTTCCTTCCTTAC[C/T]CTTCCTTCCTTACTC | 10277 |
rs571529265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10090185 | AGTGCAGAGGTGCCA[C/T]TGTGGCTCACTGCAG | 10277 |
rs571542206 | snp | A/G | 0.000367021 | 0.0135416 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106459 | CCCCCTGCCCTCGCC[A/G]GTAGCCCCCAAGCAG | 10277 |
rs571548615 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE4B | GRCh38.p7 | 1:10148119 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10277 |
rs571598132 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179206 | GTTCCCTCCCCCCAG[C/G]AGTAGCTGACAAAGA | 10277 |
rs571602739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10155240 | TCTTTCCTCTTTGCC[A/G]TGTGTGCCCTCTGGC | 10277 |
rs571701624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10143047 | CAGGAGGTAGAGGTT[A/G]CAATGAGCTGAGATC | 10277 |
rs571734677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092350 | CTGCCTCAGATTCCC[C/G]AGTAGCTGGGACTAC | 10277 |
rs571752038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047821 | TACATCTCCTTGGCT[A/G]GAGCTTAGTCTCCTG | 10277 |
rs571759214 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144850 | GCGAAAACAAACAAC[C/T]GCGTGTGAGAGTCAG | 10277 |
rs571770042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113327 | AGGGATCTGCCCCCA[A/T]GATCCAGTCACCTCC | 10277 |
rs571803878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113789 | AGATGCTTTTCGGCC[A/G]GACGCAGTGGCTCAC | 10277 |
rs571827677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10113239 | CCAGACTCTTTTAAA[A/C]AACCAGATCTCACGT | 10277 |
rs571835429 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108083 | TCTGAGGCATGTTTT[A/C]TTAAGTACAGTTGCA | 10277 |
rs571842004 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162982 | CTCACCTTTCTCCTT[A/C/G]CTTCTGTAACACCCA | 10277 |
rs571854428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155951 | ATTGCTTGAACCGGG[A/T]CCTGGGAGGTGGAGG | 10277 |
rs571864731 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037973 | TGGCTGGGATTCCGG[G/T]TGTGGTCAAGATTTT | 10277 |
rs571867941 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174070 | AACAAACACACATGT[A/G]CCAGTGACACATGGA | 10277 |
rs571879623 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074779 | TGTTAGGATTCAAGG[C/G]CTCAATATTTAACCT | 10277 |
rs571897027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061405 | GATTACAGGCATGCA[C/T]CACCACGCCCAGCTA | 10277 |
rs571900447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089204 | TAGAGACAGGGTTTC[A/G]CCATATTGGCCAGGA | 10277 |
rs571941174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10082031 | ATTCTTATCCCTCCA[A/G]ATTTGCTTGATATGT | 10277 |
rs571943308 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051553 | CCCGACCCATTAGTT[C/G]CAAAAATCTCTTCTC | 10277 |
rs571943836 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099236 | GACAGAGCAAGACTC[-/T]GTCTAAAAAAGAAAA | 10277 |
rs571957407 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175647 | CAGAGCGAGACTCCG[C/T]CTCAAATAAATAAAT | 10277 |
rs571975951 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10083055 | TTTTTAATCTATCAT[A/C/T]GATGGGCATTTGGGT | 10277 |
rs572055835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118953 | AGTGGTGCAATCTTG[A/G]CTCACTGCAATCTCT | 10277 |
rs572060095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136162 | TTATACAATACATCA[A/G]TAAGGAACATCACCA | 10277 |
rs572115878 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033092 | ATCCTCCCCCTCCCC[A/C]CTACCCGGGCTCCGG | 10277 |
rs572133517 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138764 | CCTCAGTTACCAGAT[A/T]AAGAAAATTTCCTTT | 10277 |
rs572147918 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10087002 | TAGTACTTAGGTATG[-/C]TAAAAGTGGACAAGA | 10277 |
rs572155473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10060739 | TGTATTTTAGAATCC[C/T]TAGTGAGCTAGTGAG | 10277 |
rs572157972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133901 | CAAAAAAAATAAAAA[A/G]TTAGCCAGTATAGTG | 10277 |
rs572159676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162415 | CCTGACCTTGTGATC[C/T]GCCTTCCTCGGCCTC | 10277 |
rs572160469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10134540 | AGAAAAGAAAAGAAT[A/G]TATAAAATGCCTCTT | 10277 |
rs572190287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053309 | ATGCACCACCATGCC[C/T]GGCTAATTTTTTTGT | 10277 |
rs572192134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10061449 | TTTATTAGAGACGGG[G/T]TTTCACCATCTTGAC | 10277 |
rs572195224 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180683 | ATAAAGAAAATCCTG[C/T]TGCTCTGGTCCTTGT | 10277 |
rs572222134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10163468 | ATGTCAAGAGATCAA[G/T]AACATCCTGGCCAAC | 10277 |
rs572240181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038205 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 10277 |
rs572242877 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE4B | GRCh38.p7 | 1:10175409 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCGG | 10277 |
rs572254666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10075189 | CAGCCATAGAACATA[C/T]GTAAATGAGCAAGTG | 10277 |
rs572276945 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10127779 | TAGGAAGACAAGGTC[C/T]CTCTCCTCAAGGCAC | 10277 |
rs572307080 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10103986 | AGGATGGTCTCGATC[-/T]CTTGACCTCGTGATC | 10277 |
rs572320741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10168622 | AAGGTGCCGGGTGCG[A/G]TGGCTCACGCCTGTA | 10277 |
rs572357950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128824 | TTATGTTTATGTCCC[C/T]AAAAAGTGTTTTTCA | 10277 |
rs572364396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10129714 | GGAGTGCAGTGGTGG[A/G]ATCTTGGCACACTGC | 10277 |
rs572373796 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10040478 | CTGGTCTCAAACTCC[C/T]GGGCTCAAGTGATCT | 10277 |
rs572454631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069534 | GTAAGGAAGATACTG[G/T]TTTTTTTCTTATTTT | 10277 |
rs572462127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10092444 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10277 |
rs572472907 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10173560 | GACTATATAATACTG[C/T]ACTGATTTAGAAACA | 10277 |
rs572483099 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165179 | TCACTGTGTCCAAAA[C/T]GGAACCCTTGATGTT | 10277 |
rs572495075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121674 | GCTGGTATTGCAGGC[C/G]TGAGCCACCGTGCCT | 10277 |
rs572502369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085129 | GTTCATACCTGGAGA[C/G]CCTTAACATTAAGCC | 10277 |
rs572504572 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133567 | CTAGAGAAACAATGT[A/C]ACATGATAAGAAGTG | 10277 |
rs572515003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10036820 | TGAAACTTCAAGCTT[A/G]TATTTCAGGGTTAAA | 10277 |
rs572545447 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10173742 | CTTGGAAGAGCTGTT[C/T]AGTGTGCGCCCTCTC | 10277 |
rs572550915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10106026 | CGTCTTGTAAGTATA[A/G]CCTCTAGATCAATAG | 10277 |
rs572555917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174092 | ACACATGGAGAGAAA[A/G]GCATATTTTAAGAAG | 10277 |
rs572565890 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE4B | GRCh38.p7 | 1:10111503 | ATTATATAGAACACA[C/G]ACGCACCCATGCACG | 10277 |
rs572583238 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043095 | GCTCACTGCAACCTC[C/T]GCCTCGGGGGTTCAA | 10277 |
rs572595958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10098196 | ATAATACAATATAAT[A/G]TAAATATAGTATATC | 10277 |
rs572596908 | in-del | -/AC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036081 | TTACTCCTATAAATT[-/AC]TTTTTTTTTTTTTTT | 10277 |
rs572616553 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047781 | ACAGGCTTGAGCCAC[C/T]GCCCTTGGCCCATAT | 10277 |
rs572617761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10167047 | TGAGACATGAGAATC[A/G]CTTGAACCTGGGAGG | 10277 |
rs572651153 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107965 | AAAACAGATTAAAGA[C/T]CAGTCATCAAGTTTA | 10277 |
rs572701620 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE4B | GRCh38.p7 | 1:10175488 | AACCCCATCTCTACT[A/G]AAAATACAAAAAATT | 10277 |
rs572713895 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117658 | ATTTGTTTGATTATC[C/G]CCACCCCTGGAGCAT | 10277 |
rs572722699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043485 | AGGCTGGAGTGCAGT[A/G]GCGCGATCTCGGCTC | 10277 |
rs572726934 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10177990 | CTGGGTCCACGGTGG[G/T]CGCCTGACCTCCACT | 10277 |
rs572769123 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097707 | CCCAGCTACTTTGGA[A/G]GCTGAGGCAGGAGAG | 10277 |
rs572777961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10079390 | GTCTTGAACTTCTGA[C/T]CTCAAGTGATCCTCC | 10277 |
rs572779250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145408 | GGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 10277 |
rs572785001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10084480 | ATAACCAGTAGAGAT[C/T]GTGCCACACAAACCA | 10277 |
rs572787232 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165724 | CTTCCCTCAGATTTT[C/T]CGACTCCTTCAGATA | 10277 |
rs572808582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10132264 | AAATGAGTAGAAGTG[A/G]GAGAGGAGAGAACGT | 10277 |
rs572836746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042924 | TCATTCTTGAGCTGT[G/T]CCAGGAATAGCAAGG | 10277 |
rs572868945 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10087104 | TTCTCGTCTGACGCA[G/T]ACAGGTGTATCTATA | 10277 |
rs572871529 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131761 | TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 10277 |
rs572932904 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174880 | GAAGGATGGATGGTT[A/G]GCAAGCACTGGGGAA | 10277 |
rs572943291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125390 | TTATCTGGCATATGA[A/G]AGCAAGTTACATCTA | 10277 |
rs572955601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056909 | ATGGCTCACTGCAGC[C/T]TCAGCCTCCCCAGCC | 10277 |
rs572957624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10152012 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 10277 |
rs572968078 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10109256 | CATAGAAATGCATTC[A/C]GACTTGAGCATCCTG | 10277 |
rs573007399 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126166 | TAGCCAGGTGTGGTG[A/G]CACATGCCTGTAATC | 10277 |
rs573089711 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | UBE4B | GRCh38.p7 | 1:10049601 | AAAAAAAATTTTTTT[A/T]AATTAGGAAACAATG | 10277 |
rs573090700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093905 | TCACCACATTGGCCA[C/T]GCTGGTCTCGAACTC | 10277 |
rs573130408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094475 | GTCTTGCTCTGTTGC[C/T]CAGGCTGGAGTGCAA | 10277 |
rs573135095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10042627 | ACTCTAGCCTGGGCG[A/T]CAGAGTGAGACTGTG | 10277 |
rs573168700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103577 | AGCTGGGACTACAGG[C/T]GTGCACCACCACGCC | 10277 |
rs573170373 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10104047 | TTACAGGCTTGAGCC[A/C]CCGAGCCTGGCCTTA | 10277 |
rs573183932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10058081 | CTGAGGCCAGGAGCC[A/G]ACATGGATGATCCCC | 10277 |
rs573225281 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072423 | AATTGCTTTTCTTTC[C/T]ATAACTTCCATCTTT | 10277 |
rs573255832 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE4B | GRCh38.p7 | 1:10133082 | AGGAACAGACCCAAG[A/G]GGGCAGCCAGGAACA | 10277 |
rs573256132 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10052216 | GGACTATAGGTGCAT[A/G]CCACCATACCTGGCT | 10277 |
rs573266188 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178109 | CCTGACATGTGCTAG[G/T]GCTGAACTAAATGAG | 10277 |
rs573298257 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177609 | TGCAGTGAGCCATGA[C/T]TGCACCACTGCACTC | 10277 |
rs573349784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147482 | TGGGCGACAGAGCGA[A/G]ACTCTGTCCCCACCC | 10277 |
rs573351737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10140627 | GCTGGCTTTAGAGGG[G/T]CCATTTCAATGGAAC | 10277 |
rs573382043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10159593 | AGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 10277 |
rs573389569 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069246 | CCAATGATAATGATA[A/G]CGTCAACTAATAAAT | 10277 |
rs573392567 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091954 | CAGGGTCTCTGTGTT[G/T]CCCAGGCTGGTCTCA | 10277 |
rs573440480 | in-del | -/T | 0.351853 | 0.228311 | intron-variant | UBE4B | GRCh38.p7 | 1:10041336 | ACCTTTTTGGCATTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs573451438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10152996 | GGTGTCTCTCTCGGG[C/G]GTTGTGCACGGTTGC | 10277 |
rs573462359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117696 | TTTATTCAATCAGTA[A/G]AGCAATTATTGAGCA | 10277 |
rs573475406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10160374 | ATTGGTGAGTATATG[A/C]GTTTTTCCTGTTCTA | 10277 |
rs573500423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10102731 | TGCTCTTTTATGCTC[C/T]CCATAGATTGTATTG | 10277 |
rs573525646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125594 | TTTTCTAGTGGCTAC[A/G]TAGTATACTCCTATT | 10277 |
rs573531307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10037553 | TCAAGGTGGTGCTGT[C/G]AGTAGGTGGTGTGTT | 10277 |
rs573590608 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBE4B | GRCh38.p7 | 1:10126087 | GGGTGGATCACGAGG[G/T]CAGGAGTTCGAAACC | 10277 |
rs573594030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059096 | TTAGCCAGGTGTGGC[A/G]GTGGGCGCCTGTAGT | 10277 |
rs573600212 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10073183 | TGATGGGTTCAGGAT[G/T]CCAAATGTGATTTTC | 10277 |
rs573604984 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132165 | ACTGCCTACCTCCCC[C/G]ACTCCATATTCTGCT | 10277 |
rs573629078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174664 | CCGAGATCGTGCCAT[G/T]GCACTCCAGCTTGGG | 10277 |
rs573642730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10139871 | GTAGCTGGGATTACA[A/G]GCATGTGCCACCACG | 10277 |
rs573664627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10179297 | AACCTGGGGGCCTCA[C/G]AGGGGCCCTTTGATT | 10277 |
rs573665525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10044693 | CTCAAGCGATCCTCC[C/T]ACCTCAGCCTCCTGA | 10277 |
rs573725096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118374 | ATGGAGTCTCGTTCT[C/G]TCACCCAGGCTGGAG | 10277 |
rs573725814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081280 | GGTCAGGCTGGTCTC[C/G]AACTCCCGATGTCAG | 10277 |
rs573748058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10146094 | CACAATTAACAAGGG[A/G]CCCTTATCTGGGGTC | 10277 |
rs573756177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085909 | ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 10277 |
rs573763041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10074154 | CAGAACCTAGGCAGG[A/G]AACCTCCATCAGCCT | 10277 |
rs573763512 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180818 | TTTTTTTTTAATGCT[A/G]CGTGACAGTTTGAAA | 10277 |
rs573769288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10082249 | CATGCCCGTCATCCT[A/G]GTGCTTTGGGAGGTC | 10277 |
rs573811234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094834 | CTCGCTCTGTCACCT[A/G]GGCTGGAGTGCGGTG | 10277 |
rs573822230 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122467 | TAAGATTAACTTAAT[C/G]ACCATATTAGCTCAT | 10277 |
rs573826219 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148956 | GGGGAGAAAAAAAAG[A/G]AATCAAGAAAAGGAA | 10277 |
rs573839031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10050755 | TAGAGGTGGAGTTTC[A/G]CTATGTTGCCATGTT | 10277 |
rs573850370 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10087872 | AAGTACATATGTAAT[C/G]TGGAATTCTATGAGG | 10277 |
rs573860020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10088466 | CTGCAACTTCCGCCT[C/G]CCGGGTTCAAGAAAT | 10277 |
rs573860914 | snp | A/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181607 | TGACGTCAGGAATTC[A/G/T]AGACCAGCCTGGCCA | 10277 |
rs573910619 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147229 | GGCGCAGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs573929089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153629 | GTTCGAGACTAGCCT[A/G]ACCAAAATGGTGAAT | 10277 |
rs573948074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10141506 | TAGACTTCCAGAACT[C/G]TAAGACTATAATTGT | 10277 |
rs573980414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10038252 | ACCACTACACTCCAG[C/T]CTGGGCAACAAGAGT | 10277 |
rs573992053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10080366 | CAGAGGTTGCAGTGA[A/G]CCAAGATCCCACCAC | 10277 |
rs574014560 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141966 | ACTGGAGCTGCTCCT[A/T]TCCTTTAACAACAGT | 10277 |
rs574015653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089289 | GGACTACAGGCATGA[A/G]CCACCGTGCTCAGCC | 10277 |
rs574022303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10052250 | TTTTTAATTTTTTTT[C/T]TTGTAGAGACAGGGT | 10277 |
rs574034728 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10057734 | GACCCTGTCTCACAG[-/A]AAAAAAAAAAAAAGA | 10277 |
rs574090634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039058 | GAGCAAGACTCCATC[A/G]AAAAAACAAACAAAC | 10277 |
rs574106723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10066054 | CCCTCCTTCCCTCCC[C/G]CACTCCTTCCCTCTC | 10277 |
rs574136524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118753 | ATGTGATCTGCCCAC[A/C]TTGGCCTCCCAAAGT | 10277 |
rs574164085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086116 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10277 |
rs574187563 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10167965 | TGGAAGTCTCAAAGA[G/T]CTCCGATGCTGAAAG | 10277 |
rs574203017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10086357 | AGGTGATCCACCCGC[C/T]TTGGCCTCCCAAAGT | 10277 |
rs574230057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10134621 | AATATAGAATTAATG[G/T]AATGACAGTGGTGAT | 10277 |
rs574284411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147560 | GATTATGTAGTTATA[C/T]TGATAGGTGTTTTCC | 10277 |
rs574303262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10111671 | TTGCTATTAGAAAAT[A/G]CAAGGCCAGGCGCGG | 10277 |
rs574303392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103740 | GGTTCAAGCAATTCT[C/T]CAGCCTCAGCCTCCC | 10277 |
rs574341664 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE4B | GRCh38.p7 | 1:10151094 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 10277 |
rs574341993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104085 | TTATGAAGTATAGAT[A/G]TAGTGGGTGGTCTCC | 10277 |
rs574348873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100618 | GGAGTGCAATGGTGC[A/G]ATCTCGGCTTACCGC | 10277 |
rs574353582 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042322 | GACAAACGTTGCTGT[A/G]TGGAGCTTCGTCCTA | 10277 |
rs574372307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055073 | TTACAGGTGTGAGCC[A/T]CCGCACCCGGCGTGT | 10277 |
rs574410608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055509 | TTTTTGTAGCGATGG[C/G]GTCTCGTTATGTTGC | 10277 |
rs574443367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10041750 | TCCCCATGCTGGAGT[A/G]CAGTGGCACGATCTC | 10277 |
rs574444290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093798 | CTCCCAAGTTAATGC[A/G]ATTCTCCTGCCTGAA | 10277 |
rs574456229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144599 | AATTAGCTGGGCATG[A/G]TGGTGAGCACCTGTA | 10277 |
rs574469277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048593 | AGTCTAGAGAGCATG[G/T]AATCTGGTGTCCAGG | 10277 |
rs574561143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122434 | TAAGTAGTGTCAAAA[A/G]TTCATTCTCTGAGTT | 10277 |
rs574601764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10156486 | CTCAAGTGATCTGCC[C/T]ACCCGGGCCTCCTGA | 10277 |
rs574618327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10070108 | GGTGAGATGCCATGT[C/G]TACAAAAAATTAAAA | 10277 |
rs574619999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10034564 | CTCTTCCTTTTTGCA[A/G]ATTAGGAGCTTCCCT | 10277 |
rs574648863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10150890 | AAATAGGCTGGGCGC[A/G]GTGGCTCATGCCTGT | 10277 |
rs574670952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10114118 | TCTTCCCAGAAATGT[A/C]AAGATGTGAGAAGAA | 10277 |
rs574717288 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10175606 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 10277 |
rs574792217 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164704 | ATTTGGCTTTGAAGT[C/T]ACTTTCTACCTCCCA | 10277 |
rs574833204 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10152030 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGGT | 10277 |
rs574839894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10115972 | GGTCCATCACAGAGT[A/G]AAATGTTGTTATGTG | 10277 |
rs574845253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10145557 | GTGAGCCAAGATGGC[A/G]CCACTGCACTCCAGC | 10277 |
rs574890175 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10131212 | CCGGGTGTGATGGCT[C/G]ATGCCTGTAATCCCA | 10277 |
rs574899061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10042771 | GGCCTACAGGTACAG[A/G]GAACAATCAGATATG | 10277 |
rs574899202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10177142 | GATGATACATGTATC[A/T]TTGGATATATGATTT | 10277 |
rs574920658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10158905 | ATCCTAGCTACTTGG[A/G]AAGCTGAGGCAGGAG | 10277 |
rs574960503 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079880 | TGCTTCCATTCATGC[-/A]ACTTGAATAGTTAAT | 10277 |
rs574969356 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10078528 | TTCCCCTATCTTTAG[A/T]TGATTTGTGATTGCT | 10277 |
rs574977087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10159465 | ATCAGGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 10277 |
rs574982517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10173000 | ATACCATAGAGCCTC[A/G]ACGTGGTGTAGGCCA | 10277 |
rs574998474 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10076660 | TTGGGCTGTTTTCAG[C/T]TGCAAGTAACTAAAG | 10277 |
rs575014500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071177 | CCCAGAGTGCTGGGA[A/T]TACAGGCGTGAGCCA | 10277 |
rs575015944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10049771 | GGCATGCACCTGTGG[C/T]CCCAGCTACTCGGGA | 10277 |
rs575060379 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE4B | GRCh38.p7 | 1:10035060 | CTGCAGTGCAGTGGC[A/G]CGATCTCGTCTCACT | 10277 |
rs575095685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10071818 | CTATAGGCAGGCACC[A/G]CTGAACCTGGCCAAA | 10277 |
rs575101508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10137918 | TTAAATCACTTACTA[A/T]TTCTTTTTTTTTTTT | 10277 |
rs575102138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10131595 | TAACTGCCGGCTGGG[C/T]GTGTTGGCTAATGCC | 10277 |
rs575102265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10058090 | GGAGCCGACATGGAT[A/G]ATCCCCTTCTAGAGG | 10277 |
rs575124305 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10124248 | CTCACTGCAACTTCC[A/G]CCTTCTGGGTTCGAG | 10277 |
rs575128693 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10157826 | ATTCTGAAATTTCTC[A/G]TGCCTAAGCTTTTGC | 10277 |
rs575146981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10145324 | CTCCCTTGGCCGGGC[A/G]CAGTGGCTCACACCT | 10277 |
rs575150530 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174472 | TTGGGGAGCCGAGGC[A/G]GGCAGATCACCTGAG | 10277 |
rs575172106 | in-del | -/A | 0.00797793 | 0.0626524 | intron-variant | UBE4B | GRCh38.p7 | 1:10175496 | TCTACTAAAAATACA[-/A]AAAAATTAGCCAGGC | 10277 |
rs575178068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048319 | ATGAATATGCTGCCT[A/G]TTCTTTGTCCATATG | 10277 |
rs575180815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10151142 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 10277 |
rs575188485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10048660 | CTGTGTCTAATGTTG[A/G]TAAAATTAGAGGAGG | 10277 |
rs575233842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10166102 | AATCTCCATCAAGCA[A/C]AGACTGGAGCACTTT | 10277 |
rs575266596 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172803 | GCAGTGAAAAAATAC[A/G]TAGTCATGTGCTGTT | 10277 |
rs575272876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10087012 | GTATGCTAAAAGTGG[A/G]CAAGACCAGAGCAGA | 10277 |
rs575282514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10138407 | TGGCCCAATTTTTTG[A/T]ATTTTTTGTAGAGAC | 10277 |
rs575288833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10103455 | TTTATTTATTTTGAG[A/G]TGGAATCTCACCCTA | 10277 |
rs575298113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10055634 | GTTAGAAGTAGTGAA[C/T]GCTGGCCAGGCGCAG | 10277 |
rs575307550 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066735 | ACAAGGTGAAACCTC[G/T]ACTCTACTAAAAATA | 10277 |
rs575332854 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094301 | TAAATGGATCGATCT[A/G]TATCAAAGGACATTG | 10277 |
rs575375406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115688 | TCTGAGAAATGGATC[A/G]TTAGGCAGATTGGTC | 10277 |
rs575394355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131346 | GCCAGGCATGGCAGC[A/G]CGTGCCTGTAATCCC | 10277 |
rs575414657 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10173618 | GAAAGAAAAGGGAAG[A/C]ACTTACCCATTGAGG | 10277 |
rs575431372 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036118 | GATCTGTTAATAGTC[C/T]TTGGTTTAGAGGCTT | 10277 |
rs575437891 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082539 | CAAAATCTTTCAGAT[A/G]ATGGTAATTATAGAG | 10277 |
rs575456145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10131841 | GCCTGTAATCCCAGC[A/G]ACTTGGGAGGCTGAG | 10277 |
rs575456605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144660 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 10277 |
rs575469408 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091852 | TCAAGTGATCCACCC[A/G]TCTTGGCCTCTCAAA | 10277 |
rs575476609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10174066 | GTGAAACAAACACAC[A/G]TGTGCCAGTGACACA | 10277 |
rs575482388 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072145 | GCGGCATCAGCCCCA[A/G]GACCCTCTCAGAGTC | 10277 |
rs575490172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10107825 | TCAAGTGATCTGCCC[A/G]TCTTGGCCTCCCAAA | 10277 |
rs575547731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10065011 | TCAAGTGATCCACCC[A/G]CCTGGCCTCCCAAAG | 10277 |
rs575613507 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085057 | TTAAGATAAAGTTAC[A/G]ATTTTGAAATCTTTG | 10277 |
rs575615358 | in-del | -/GAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080446 | AAAGAAAGAAAGAAA[-/GAAA]ATTCTATGTTGGTGA | 10277 |
rs575620896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100949 | TTTAGATCCTAATTT[A/G]TGAAGAACTCTTAAA | 10277 |
rs575642625 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072231 | TAAGCCCAAGCTTCA[C/T]ACCTGGGACTCTTTT | 10277 |
rs575643440 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136157 | AGATTTTATACAATA[C/T]ATCAGTAAGGAACAT | 10277 |
rs575677169 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10051875 | TCATTGTATTAACTA[-/CTC]AACAGCTGCTAAATC | 10277 |
rs575691417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10106712 | TATTAACCTGTGTGG[C/T]TAACTAGTTTGGTAG | 10277 |
rs575744725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10152911 | GATCTCAGAACCCAG[C/T]TGCCCTGATGAGGGC | 10277 |
rs575824450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064386 | GCAAACTGCTGATCG[C/T]ATCTCCGAGGAATTG | 10277 |
rs575834263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043583 | AGGCGCCCACCACCA[A/T]GCCTGACTAATTTTT | 10277 |
rs575880874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075228 | TTCCAGTAAAACTTC[A/G]CTTACAAAAACAGGC | 10277 |
rs575903174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10153688 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10277 |
rs575913864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10125232 | ATATTTTACTTGTAG[C/T]CTCCCTAAAAAAATT | 10277 |
rs575915031 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10075834 | AGGTGGGAGGATCCC[C/T]TGAGCCTAGGAGTTC | 10277 |
rs575934269 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117466 | CTCTGAAGTTTGGGA[A/G]CCTCTGGTGGAGCAA | 10277 |
rs575966509 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049120 | TAGAGCTTAAAAAAA[C/T]AGTTGAGTGGCAAAT | 10277 |
rs575967408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10159004 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10277 |
rs576055583 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048701 | GACTATGGGATTTGG[C/T]GACATGGAGGCCCTT | 10277 |
rs576134463 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031492 | CACTGTACACCTTAA[C/T]TGGGTGAATTGTATG | 10277 |
rs576144081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10155415 | ACTGAAGCTTAAAAG[A/G]GTCAAGAAGCTTGCT | 10277 |
rs576161429 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031322 | GACCTCTTGATCCAC[A/C]CGCCTTGGCCTCCCA | 10277 |
rs576162300 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168943 | TAACAGCTGTTGACA[A/G]TGGAAGGATATTAAG | 10277 |
rs576198834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053782 | GCAGCCTCGACCTTT[C/T]GGGCTCAAGTGATCC | 10277 |
rs576218342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169950 | AACCCAAAAGGCAGA[G/T]GTCGCAGTGAGCCGA | 10277 |
rs576234855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169428 | GGGGACAACTCTTTT[A/C]CACTCTTTTAACTTT | 10277 |
rs576274966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10068464 | AAGTGATTCTCCTGC[C/T]GCGGCCTCCTCAGTA | 10277 |
rs576302243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10060916 | GCCCAGCTAATTTTT[A/T]AAATTTTTTTGTAGA | 10277 |
rs576331962 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109172 | CCCCTTTACTCCTCG[C/T]TGTAGCCTGCTGTGA | 10277 |
rs576353325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10121716 | CTTTTTTCAGTGCTT[A/C]ATTTTTAAAGGGCTC | 10277 |
rs576364450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10122577 | TGGTATTTATACATT[A/G]TTTTGGTATCTCATT | 10277 |
rs576366951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10162038 | AGTTTCACTCTTGTC[A/G]CCCACGCAGGAGTAC | 10277 |
rs576372311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10136804 | CACGCCTGTAATCCC[A/G]GCTTACTAGGGAGGC | 10277 |
rs576405044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172211 | CGATTTAGGCTAAGC[G/T]GTCCCTGCGTGATCT | 10277 |
rs576413191 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136483 | AGTAAGACCCTCTTA[-/A]AAAAAAAAAAAAAAA | 10277 |
rs576417045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10164522 | GGCTGGCCAGCGTAT[A/G]TTTTAGATGTTGGAA | 10277 |
rs576419455 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086127 | CAGGCGCCCGCCACC[A/G]CGCCAGGCTAATTTT | 10277 |
rs576428452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10162544 | GACTCCTGACCTCAG[G/T]TGATCCATCCGCCTC | 10277 |
rs576476183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10063158 | CTGTAGTCCCAGCCA[C/G]TGGGGAGGCTGAGGC | 10277 |
rs576485720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092622 | CACCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 10277 |
rs576501411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165272 | CTCAGGCTCGATGCT[G/T]TGGAGTTGCTCTTGA | 10277 |
rs576503037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115105 | AGACTCTGGGCTGAA[C/T]GCCTTGAATTTCAAA | 10277 |
rs576553350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10077348 | CTGTGTCCAAATTTC[C/T]CTCTTATGACAGCCA | 10277 |
rs576553661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10069654 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 10277 |
rs576562341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10040529 | GTGCTGAGATTGCAA[A/G]TTTAATTTTGGACCA | 10277 |
rs576565151 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176555 | AAATTAAACATGTTA[A/G]TTTGTTTTTGTTTCT | 10277 |
rs576594969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10092578 | TATGCCTGTAATCCT[A/T]ACACTTTGGGAGACT | 10277 |
rs576650455 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175517 | TTAGCCAGGCGTGGT[A/G]GCGGGCGCCCGTAGA | 10277 |
rs576657010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171429 | TAAATGAAGATGAGT[A/G]GGTTGTTTTCCTTTG | 10277 |
rs576685134 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE4B | GRCh38.p7 | 1:10086045 | GGCACAATCTCCGCT[C/T]ACTGCAAGCTCCACC | 10277 |
rs576701918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10069434 | ATACACAAATAAATA[C/T]ATCACACATGTCATA | 10277 |
rs576704285 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033261 | AGGGTAGGAAGGAGA[C/G]CAGGATCTGCTGTAG | 10277 |
rs576724905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10054973 | GTATTTTTAATAGAG[A/T]TGGGGTTTCTCCATG | 10277 |
rs576740925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10106764 | TTCTGCCAGGCTCTA[A/G]TCATGCTGGAAAGTT | 10277 |
rs576751538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10062309 | AATACATTCGATGTG[C/T]GTTTTTTTGTTTGTT | 10277 |
rs576772642 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133042 | AAGCTGCTATGTAGA[C/T]GGACCAAAACAGAAG | 10277 |
rs576780576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10175686 | AAATAAAAAAGAAAA[G/T]AAAAAAAATAAAAAT | 10277 |
rs576789764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10115277 | CAGGCATGAGCCACC[A/G]TGCCCAGCAAATATC | 10277 |
rs576789879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10123722 | AAGTCCTGCATTTTT[A/T]AAATTAAGATGAAAT | 10277 |
rs576791829 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10054724 | CCATGGTAACACTTG[C/G/T]GGGGCATTTTTTTTG | 10277 |
rs576818419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10076815 | GCAATGGCATGATCT[C/T]GACTCTCTGTAACCT | 10277 |
rs576863308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10047554 | CTGGAGTGTAGTGGC[A/G]TGATCTCGGCTCACC | 10277 |
rs576873131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150255 | ACACGTGATTTTGAT[G/T]GGTATGAAATTTTAA | 10277 |
rs576908985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10136387 | AGGCAGGAGGATTGC[C/G]TGAGCCCAGGAAATT | 10277 |
rs577009631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10150772 | GGCTGAGGCAGGAGA[A/C]TCGCTTGAACTTTGG | 10277 |
rs577011061 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10093083 | AGTATTATTGTACAC[A/G/T]TACTATACTATACTA | 10277 |
rs577022396 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10126352 | AGATAGATAGATAGA[-/T]AGAAAGGAGGAAATA | 10277 |
rs577024620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10144060 | AACATCATGATAGAA[A/G]GGGGTTGAAATAGTG | 10277 |
rs577066348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10156353 | CAAGTGATCCTCCTA[C/T]CTCAGCCTCCCCTGT | 10277 |
rs577077323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10120997 | AAAACTTTAAAAAAC[A/G]TTCCTTGATTAAAAT | 10277 |
rs577090076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10053883 | TTGTAGACAAGGCCT[C/T]GCTATGTTGCCCAGG | 10277 |
rs577102402 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE4B | GRCh38.p7 | 1:10114030 | AGATTGTGCCACTGC[A/G]CTCCAGCCTGGGTGA | 10277 |
rs577145091 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141531 | AATTGTGTGGTTTGG[A/T]GCCACTGAGGTTGTG | 10277 |
rs577198627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10165382 | AGACCGTTGGCATCT[C/T]TTACCTGGGTTATTG | 10277 |
rs577223372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10118823 | CAGCTAATTTTTATG[C/T]TTTTTTTAGTGGAGA | 10277 |
rs577259610 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE4B | GRCh38.p7 | 1:10158165 | TCATTGTCAAATCTT[C/T]ATTGTGAAACTTTTG | 10277 |
rs577271996 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | UBE4B | GRCh38.p7 | 1:10173497 | AAAAAAAAAAAAATT[-/A]TATATATATATACAC | 10277 |
rs577288656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10056354 | ATGGAGAAAACTGCT[A/G]GGCTGAAATTATTTT | 10277 |
rs577350263 | in-del | -/AAC | 0.00398564 | 0.0444627 | intron-variant | UBE4B | GRCh38.p7 | 1:10154250 | TCATCTCAAAAACAA[-/AAC]AAAAAACAAAACAAA | 10277 |
rs577360606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10085456 | GACCTGAGGGGAAAG[A/C]CTTTGTGAAGGGTCA | 10277 |
rs577371514 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045065 | TAAGGAGGGTGCAAT[A/G]TAGATCCCTCGCGTG | 10277 |
rs577405027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10095896 | CCTGCCTCAGCCACC[C/T]GAGTAGCTGGGATTA | 10277 |
rs577438614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10064287 | TGATTCAGTTATTAC[A/G]TGAATATACAGTTAG | 10277 |
rs577456075 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059506 | CTCCCGGAAGGGGCC[A/G]TCATGGAGCTGAGCC | 10277 |
rs577458903 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131266 | TGGATCACCTGAGGT[C/G]AGGAGTTTGAGAACA | 10277 |
rs577468429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10078152 | TAGCTGGGGTTACAG[A/G]TGCGTGCCACCACAC | 10277 |
rs577496021 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073013 | AGTTTTTGTTGCTGT[A/G]CTTCTCGTTAGGTAT | 10277 |
rs577519310 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077521 | GCCTTGCCAGTGTTG[C/T]TCATCCCCTTACCCC | 10277 |
rs577553343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10176436 | GTTTTCTACAGCTGC[C/T]GCCCATTTGACATTC | 10277 |
rs577559188 | snp | A/C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075356 | TCTCATCACCTCCAC[A/C/T]GCTATTACCCAGGTC | 10277 |
rs577599770 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097920 | TGTCTCCCATACTGG[-/A]AATGCCGTGGCACAA | 10277 |
rs577602350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10089067 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 10277 |
rs577619936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10039657 | GTTGACTAGGCTGGT[C/T]TCAAACTCCTGACCT | 10277 |
rs577627798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10172906 | CTGTGTTTAGAATAC[A/T]CACCATTGTGTTACA | 10277 |
rs577633587 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059631 | TAAAGCCATGGAAGC[A/G]TGGCTGCTTAGGGCA | 10277 |
rs577680529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10059733 | TGCCTCTCACCTCCA[C/T]GTGTCACAGTGACCA | 10277 |
rs577687245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10161817 | GTGCTCTTTCCTGAC[A/G]TGCGTAGCAGCCACT | 10277 |
rs577689852 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094724 | CAGGTGTGAGCCACC[A/G]CACCCAGCCTCATTA | 10277 |
rs577710420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10111723 | GCACTTTGAGAGGCC[A/G]AGGTGGGCGGATCAC | 10277 |
rs577732767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10036995 | TATGTGCACTTTTTG[G/T]TCCCTGTCATAGATC | 10277 |
rs577735573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10169840 | GCCAACATGGCGAAA[C/T]CCCGTCTCTACTAAA | 10277 |
rs577766523 | in-del | -/AAAAC | 0.00199481 | 0.0315187 | intron-variant | UBE4B | GRCh38.p7 | 1:10055922 | AGACTCTGTCTCAAA[-/AAAAC]AAAACAAAACAAAAC | 10277 |
rs577788146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10066309 | TTTTTTGTGGGATTG[C/G]GGGGGGAGGGGGTCT | 10277 |
rs577832562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081283 | CAGGCTGGTCTCCAA[C/G]TCCCGATGTCAGATG | 10277 |
rs577850454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10154642 | CAGGAGTTGGAGGCT[C/T]AGTCTGGCCAAAATG | 10277 |
rs577852461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10147825 | CCTCCAGGCAAACCA[A/T]TTTTGTTTTATTTAT | 10277 |
rs577860460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10081963 | CAAGTGATCTTCCCA[C/G]CTTGGCCTCCCAATG | 10277 |
rs577875872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10043972 | AAACAGGAGGTGGGG[G/T]GTCCATTTGCTGTTT | 10277 |
rs577902612 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121918 | TCACGTGCCTCTGTA[A/G]TGAGTTGACTTCATC | 10277 |
rs577907166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10133778 | CATCTGGGCATGGTG[G/T]CTGGTGCATGCCTAT | 10277 |
rs577914581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10148358 | TCAAGAAGGCTGGGC[A/G]TGGTGGCTCACGTCT | 10277 |
rs577916735 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091532 | CCACTGCAGCTTCTA[A/C]TTCCTGGGCTCAAGC | 10277 |
rs577918744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10037581 | GTTTATTTTTGAGAT[A/G]GGGTCTGGCTCTATC | 10277 |
rs577933714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10142562 | TGTAGTCCCAGCTAC[C/T]CAAGAGGTTGAGGCA | 10277 |
rs577972333 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031580 | TCACCAGGGGTTCAA[G/T]TTCTGGCTTACACAG | 10277 |
rs577978803 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118269 | TCATATTTGTAAAGG[G/T]CCTTCTTTGGGCTTT | 10277 |
rs577991280 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE4B | GRCh38.p7 | 1:10083298 | ACAGAAGGAAAACAG[A/G]TGCAAAGGTCCTGGG | 10277 |
rs578013025 | snp | A/T | 1.64803e-05 | 0.00287052 | intron-variant | UBE4B | GRCh38.p7 | 1:10129386 | TGACTCTGATCTTAT[A/T]TCTAGGCACTAGGTG | 10277 |
rs578022407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10135474 | CTGGGCATGGTGGCA[C/T]ACGCCTGTAATCCCA | 10277 |
rs578034206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10075869 | CCAGCCTGGGCGACA[G/T]AGCAAAACCCCGTCT | 10277 |
rs578051903 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160698 | ATCTCTGTAATCCCA[A/G]CATTTTGAGGGGCTG | 10277 |
rs578083967 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140643 | CCATTTCAATGGAAC[C/T]ATCTAGAACCTTTGC | 10277 |
rs578095989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE4B | GRCh38.p7 | 1:10112353 | TTTGTACAGCTGAGG[A/G]AAAATATTAAATACT | 10277 |
rs578109030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10104117 | GGGATCCTGAGAGAA[A/G]TGTTCTGTATGAGCT | 10277 |
rs578122360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10105176 | TTACAATTAATATAC[A/G]TCAGCGGTAACTCTC | 10277 |
rs578131759 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126206 | TCGGGAGGCTGAGGC[A/G]GGAGAATCACTTGAA | 10277 |
rs578134092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE4B | GRCh38.p7 | 1:10128008 | TGGATTTATGCCAGA[C/G]CTCTTTCCATTGTAC | 10277 |
rs578225515 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE4B | GRCh38.p7 | 1:10097046 | TCTGCATCAAAAAAA[A/T]AAAAAAAATAATAAT | 10277 |
rs745321421 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097646 | GAAACCCCGTATCTA[C/T]TAAAAATACAAAAAT | 10277 |
rs745346204 | snp | C/T | 1.65198e-05 | 0.00287395 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103049 | CAGAGATGTCATCTT[C/T]CTTTCTTCTCTTTCT | 10277 |
rs745349207 | snp | C/T | 1.65814e-05 | 0.00287931 | intron-variant | UBE4B | GRCh38.p7 | 1:10119470 | CAGCATGGAATTGTA[C/T]TGTTTGTTTCTTGTC | 10277 |
rs745391284 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036432 | ACAAAGGGCTGGTTC[A/G]ATAACTGTTAATTTT | 10277 |
rs745406800 | in-del | -/C | 1.65176e-05 | 0.00287376 | intron-variant | UBE4B | GRCh38.p7 | 1:10119622 | GCCCAGGTATGAAGA[-/C]CCCGTGACGTGCTTG | 10277 |
rs745442655 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127413 | AGCAGGCATACATTG[C/T]GGACAGAAGCTTCAG | 10277 |
rs745446984 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140865 | TTAAGTTTTGAATCA[C/T]TTCCTCTGAATTAGA | 10277 |
rs745449550 | in-del | -/C | 6.6533e-05 | 0.00576733 | intron-variant | UBE4B | GRCh38.p7 | 1:10149172 | AATTGTCCTTTTTTT[-/C]CTCTTTGACAGTATA | 10277 |
rs745473864 | in-del | -/TTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172699 | AAGCATTGTAGGTAC[-/TTT]TTTTTAATGACAGCT | 10277 |
rs745482717 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121325 | GCGCCACCATACTCC[A/G]GCCTGGGCAACAGAG | 10277 |
rs745527896 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139190 | CACCTGAGGTCAGGA[A/G]TTGGATGCTAGCCTG | 10277 |
rs745546211 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052439 | TTAATGGACGTTTTT[A/G]GGAATTGAACTTCTA | 10277 |
rs745592201 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090795 | AAGCCTATGCATTTG[-/TG]TGTGTGTGTGTGTGT | 10277 |
rs745610889 | snp | A/G | 4.94507e-05 | 0.00497221 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105710 | AGCCCCATGTTCTGC[A/G]GCGTGGCTTCCTTTG | 10277 |
rs745624324 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090207 | TCACTGCAGCCTCAG[C/T]CTCCTGGGCTCAGGT | 10277 |
rs745635633 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075369 | ACCGCTATTACCCAG[G/T]TCCAAGGCACCAGCA | 10277 |
rs745677423 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076869 | CTCCTACCTCAGCCT[C/G]CCGATTAGCTGGGAT | 10277 |
rs745682023 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043146 | TCCCAAGTAGCTGGG[A/G]TTACAGGCATGCACC | 10277 |
rs745685880 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130616 | CTTTGCAGAAGATGA[C/T]GTAAGTATAGTGGCT | 10277 |
rs745708187 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078351 | TAGGGCTTACTGCAG[A/G]TCAGACACAGTACTT | 10277 |
rs745713634 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120244 | TAAAAGTTTAGGCCG[A/G]GCATGGTGGCTCACA | 10277 |
rs745756509 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175934 | CCACCACCTCTACCT[A/T]GTTCCACTACATGTA | 10277 |
rs745764255 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | UBE4B | GRCh38.p7 | 1:10130712 | TTTTCCTTCTCTTTC[C/T]AGGTTAAAGTGGTTG | 10277 |
rs745764403 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143769 | TACTGAATCATTGGA[A/G]TGGCTATAATAGAAG | 10277 |
rs745787031 | snp | A/G | 0.000132499 | 0.00813829 | intron-variant | UBE4B | GRCh38.p7 | 1:10179577 | GGTAGAGGAGGGTGC[A/G]GTTTGAGGTGCAGCG | 10277 |
rs745803927 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100849 | GTGAGCCACTGCACT[C/T]GGCCAATGATATACT | 10277 |
rs745814211 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158958 | GAATTTGCAGTGAGC[C/T]GAGATTGTGCCAGTG | 10277 |
rs745840536 | snp | C/T | 1.66643e-05 | 0.0028865 | intron-variant | UBE4B | GRCh38.p7 | 1:10179877 | GGGGCATTAATCCTC[C/T]TTTTTTTCTTTTCTC | 10277 |
rs745856273 | snp | A/G | 4.9694e-05 | 0.00498443 | intron-variant | UBE4B | GRCh38.p7 | 1:10158501 | AGTATGGGGCCCCTC[A/G]TGTCACAACTTGCTT | 10277 |
rs745859114 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088468 | GCAACTTCCGCCTCC[C/T]GGGTTCAAGAAATTC | 10277 |
rs745887037 | snp | A/G | 1.65556e-05 | 0.00287707 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117536 | CCTGCAAAGAGACAG[A/G]TATGCTGAACTACCT | 10277 |
rs745890114 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176448 | TGCCGCCCATTTGAC[A/G]TTCCCACTGGCAATG | 10277 |
rs745903743 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116549 | CTGTCGTAATTAATC[C/T]GTATGTGTCTTTTAT | 10277 |
rs745907594 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079778 | AACAGAATTTGTTTC[G/T]TTTCTTTGGCTGCTA | 10277 |
rs745914831 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045921 | ACAGAGAGACATGAA[A/G]TGGCAGCTGCTTAAG | 10277 |
rs745924672 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167887 | AGCCACCACGCCCGG[C/T]AGATGGTGACTTCTT | 10277 |
rs745946186 | snp | C/T | 0.000131998 | 0.0081229 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101062 | TACAGTGACATTGTG[C/T]GGATTTATAAAAGGT | 10277 |
rs745951135 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065503 | CCACGCTGCAGGGGT[A/G]GTTTCGGCCCTGTGA | 10277 |
rs745964261 | snp | A/G | 1.65378e-05 | 0.00287552 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179998 | GACACAGCCAAGGCC[A/G]ACGAGGCAAGCAGAA | 10277 |
rs745967246 | snp | A/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031443 | GTTCTGAAATTGGAC[A/G]GTGAGGATGACTGAA | 10277 |
rs745988061 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067621 | ATTAATTAGATACAC[-/T]TTTTTTTTTTTTTGA | 10277 |
rs745992038 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124031 | CCACCCGCCTCAGCC[A/G]CCCAAAGTGCTGGGA | 10277 |
rs745993689 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145742 | GATATTTGACAAAGA[G/T]TATCTGTGGTAGTGG | 10277 |
rs746001883 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114060 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 10277 |
rs746032621 | snp | C/T | 6.67134e-05 | 0.00577514 | intron-variant | UBE4B | GRCh38.p7 | 1:10134985 | TCTTTTCAACTTTCA[C/T]AGACAGATGATAGAT | 10277 |
rs746047995 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | UBE4B | GRCh38.p7 | 1:10119631 | ATGAAGACCCGTGAC[A/G]TGCTTGACATTAGCA | 10277 |
rs746050181 | snp | A/G | | | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181347 | TCTTTCCTGGATCCA[A/G]TTAGGAGCTGCTATT | 10277 |
rs746085642 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091898 | GGTGTGAGCCACTGC[A/G]CCCGGACTACCTGAC | 10277 |
rs746089869 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177718 | GGCCACTTGTTTTGC[A/G]ATGGTGATACAAATA | 10277 |
rs746101018 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105903 | GGAAGTGGAATTCTC[C/T]TTTCTAGATTATTAT | 10277 |
rs746133739 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076741 | TCTGCAGTCCCAGCC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs746134295 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122948 | GGAATTGTGTTTTCA[C/G]CAGTCTTCAAAATAT | 10277 |
rs746143172 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093651 | GTGATTGTTTTCACT[A/G]CAACGGGTAACTCAA | 10277 |
rs746157529 | in-del | -/CTTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044553 | CCTTCCTTCCTTACT[-/CTTC]CTTCCTTCCTTCCTT | 10277 |
rs746164686 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105658 | ACGGTCACCAGACAG[A/C]AATCTCTTGCTAAAC | 10277 |
rs746168688 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044666 | CAGCTCACTGTAACT[C/T]CACCGCTTGGGCTCA | 10277 |
rs746185119 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117050 | ACAAAGATGAGGGCT[A/G]TTTTGTCAGTCCCTT | 10277 |
rs746196068 | snp | A/G | 3.31895e-05 | 0.00407353 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106387 | CGGTATCGCCCCTAC[A/G]CTGTCACTCACCCAT | 10277 |
rs746204283 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10129444 | CACACCCTGTGTGCA[A/G]TTTGGTAAGCACTCA | 10277 |
rs746236857 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058456 | CTCACTGAGCTGTTA[A/G]GTTTATATGTGTTAA | 10277 |
rs746256550 | snp | A/G | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178719 | AAATCCACAATAGCA[A/G]TAGAAAAATTTAAGC | 10277 |
rs746281977 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158139 | CTAGCCCCGTTCCTT[C/T]AGGTGTTGTGTCATT | 10277 |
rs746286335 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090657 | CTGGTCTTGATCAAG[C/T]GATCCTCTTGCCTCG | 10277 |
rs746307471 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158648 | CAGGATTTTTTAAAT[C/G]GCTTTACTTGCAAGA | 10277 |
rs746313925 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058094 | CCGACATGGATGATC[C/G]CCTTCTAGAGGTGAC | 10277 |
rs746328640 | snp | A/G | 1.67531e-05 | 0.00289418 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106480 | CCCCAAGCAGTGCCC[A/G]CCAGCAGTTCCAGAC | 10277 |
rs746356019 | snp | C/T | 1.65693e-05 | 0.00287826 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178787 | CGCACGCGCAGAAAT[C/T]GACTACAGCGACGCT | 10277 |
rs746363844 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095477 | AGTAGCCCATCGAAG[C/T]CAGAGCAGTGAAGGA | 10277 |
rs746370872 | snp | A/G | 3.30011e-05 | 0.00406195 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149217 | TTCAGATGTCCCCAA[A/G]GTATTTGCAGCGTTG | 10277 |
rs746373321 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084398 | CTCTTCATGTAATTC[A/C]CTATCTTGATTTTCA | 10277 |
rs746384903 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072324 | AAGCAGACATCAGCT[C/T]TTTAAAATCCTCCAA | 10277 |
rs746392741 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116340 | TAGAAACAGGGTTTC[A/G]CCCTGTTGGTCAGGC | 10277 |
rs746416517 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069885 | GCTGTTAAGTGACTT[A/G]TCTGGATAGGCTCCA | 10277 |
rs746423754 | snp | G/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132426 | GAAACCCGTGAGGCT[G/T]CTCTCAGTTACATGG | 10277 |
rs746424092 | snp | A/T | 1.69648e-05 | 0.00291241 | intron-variant | UBE4B | GRCh38.p7 | 1:10151301 | TCTCAGCGGTCTCTT[A/T]CTTGCTCTTCTTGCC | 10277 |
rs746482786 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037951 | CCTAGTTCATCTGCA[A/G]GATGGTTGGCTGGGA | 10277 |
rs746482978 | snp | A/G | 0.000161878 | 0.00899515 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107229 | TGTGGTAGTATGTAC[A/G]ACAATCCTTTCTCCT | 10277 |
rs746485466 | snp | C/T | 1.67265e-05 | 0.00289188 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179417 | CTTTGTCCCCGCAGA[C/T]CCTCTGATGGACACC | 10277 |
rs746499957 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173214 | CCGAGCGCGGTGGCT[C/G]ATGCCTGTAATCCCA | 10277 |
rs746513099 | snp | A/G | 4.95602e-05 | 0.00497771 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179541 | AACCGGCAGACGCTG[A/G]CAGAGAGCATGCTGG | 10277 |
rs746540784 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071609 | TGTAATATGCTTACC[A/G]TAAATTCGCCATGTC | 10277 |
rs746562888 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155907 | TGGGGGCCTGTAATG[C/T]CAGCTACTTGGGAGG | 10277 |
rs746584007 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130125 | GTCACCCAGGCTGGA[A/G]CGCAGTGGCGCAATC | 10277 |
rs746615932 | snp | C/T | 1.65086e-05 | 0.00287298 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117498 | TAATTGGGATTCCTA[C/T]AGTGACCATTTCACC | 10277 |
rs746636059 | snp | A/G | 1.65146e-05 | 0.0028735 | intron-variant | UBE4B | GRCh38.p7 | 1:10158485 | TGGAGGAGTTCAAGT[A/G]AGTATGGGGCCCCTC | 10277 |
rs746642059 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128818 | GCTAAATTATGTTTA[C/T]GTCCCTAAAAAGTGT | 10277 |
rs746645379 | in-del | -/GACA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111044 | TCTTTCTCTGTCTCT[-/GACA]CACACACACACACAC | 10277 |
rs746656625 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100258 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 10277 |
rs746658838 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097821 | TCTCAAAAAAAGTAA[A/T]AAATAAATAAACACA | 10277 |
rs746660899 | snp | G/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103025 | CCGTGTCTCTTGGAA[G/T]GACCGGGACAGAGAT | 10277 |
rs746677897 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141822 | GGGAATTTAGAGATT[C/T]AGGTACTTGGAGTCA | 10277 |
rs746719344 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065338 | GTTATGGGGCAAGTG[A/G]CGGGAGGAGCATGCG | 10277 |
rs746724659 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161161 | GGGAAGCAGTTTGTT[C/T]GCTATATAAACATGT | 10277 |
rs746733354 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117622 | GAAATGGATTAACTT[-/A]AAAAAAAAAAAAGCC | 10277 |
rs746754591 | snp | A/G | 1.78608e-05 | 0.00298832 | intron-variant | UBE4B | GRCh38.p7 | 1:10106187 | TTCCTCCCTTTCTCA[A/G]CTAATTTAGCCTCTA | 10277 |
rs746757325 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109970 | TCCCAAATTGCTGGG[A/T]TTACAGGCGTGAGCC | 10277 |
rs746794603 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072941 | CTAATAATTTGATAG[A/C]CTTCTGAATCATCTG | 10277 |
rs746801529 | snp | A/T | 1.67312e-05 | 0.00289229 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144964 | AGATTTGAAAAATAA[A/T]GAAAGCCAATGGAAA | 10277 |
rs746809069 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064084 | CACCATGTCCATACA[C/T]ACTCATTCTTACCAA | 10277 |
rs746829388 | snp | C/T | 8.61898e-05 | 0.0065641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171092 | TTTTGGTCCTTTTCA[C/T]TTGTCTCAACAGCAT | 10277 |
rs746832656 | in-del | -/TTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110669 | TTGGTGGTTTTGTGT[-/TTG]TTTTTTAACTGTAAA | 10277 |
rs746838816 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152770 | ACCAGTGTGCTCCAG[C/T]CTAGGAGAAAGGGCA | 10277 |
rs746850681 | snp | A/T | 0.000280901 | 0.0118479 | intron-variant | UBE4B | GRCh38.p7 | 1:10130475 | CTGTTCAGCGGCTTG[A/T]CTGGCTCTTCCATCT | 10277 |
rs746859973 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168933 | AAGCATAAGGTAACA[A/G]CTGTTGACAATGGAA | 10277 |
rs746879668 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043269 | CGGCCTCAGCCTCCC[A/G]AAGTGCCGGGATTAC | 10277 |
rs746896512 | snp | A/G | 3.32298e-05 | 0.004076 | intron-variant | UBE4B | GRCh38.p7 | 1:10146912 | CCCAGTCCCCCTGTA[A/G]GGACTTAGCTACTGA | 10277 |
rs746907058 | snp | C/T | 0.00010293 | 0.00717318 | intron-variant | UBE4B | GRCh38.p7 | 1:10033739 | TTAGTTGGCAACTCG[C/T]TAGCGCTTTGGACAG | 10277 |
rs746922101 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148379 | GCTCACGTCTGTAAT[C/T]CCAGTACTTTGGAAG | 10277 |
rs746949110 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116987 | TCTTAACCTTTGGTT[C/G]TATTGCCAAATGTTA | 10277 |
rs746949683 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103358 | CTCAGGGTTGAAGTT[C/T]TTCTCTTTGTAGTAA | 10277 |
rs746988530 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076904 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTG | 10277 |
rs746995227 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121527 | GCCTTCCAAGTAGCC[A/G]GGACTCCAGGCACAC | 10277 |
rs747010101 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082825 | CCCCACCCTCCCCCT[A/G]TTAGGCCCCAGTGTG | 10277 |
rs747057743 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091017 | CCTTTAGCAAACTCT[A/T]CTCAGTTATAGAAGT | 10277 |
rs747082431 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033828 | ATTTTCCAAGAATAA[C/T]GTGACTCCCCGATAG | 10277 |
rs747095903 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143018 | GAGGCTGAGGTACGA[C/G]AATTATTTGAACCCA | 10277 |
rs747098604 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053543 | TGGGGTATATGGGCT[C/G]GATGTGTAAGTTTGT | 10277 |
rs747111134 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156257 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGCTAGGGTCTTGC | 10277 |
rs747131906 | snp | A/G | 3.30175e-05 | 0.00406296 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149199 | TATAACACTGCCTTT[A/G]AATTCAGATGTCCCC | 10277 |
rs747163617 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062878 | GGAGAATGGCTTGTA[C/G]CTGGGAGGCGGAGGT | 10277 |
rs747188322 | snp | C/T | 2.50875e-05 | 0.00354163 | intron-variant | UBE4B | GRCh38.p7 | 1:10132329 | GAATCATGTGCAAAA[C/T]AGTTTTAATTTGTTT | 10277 |
rs747189716 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031849 | TGTTACTTTGATCGC[C/T]CAACTTAGATTTATA | 10277 |
rs747195185 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169347 | ATTTGCTCTTACCTT[C/G]GTTATGTGACTCTCT | 10277 |
rs747212608 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137681 | GCCAGATAGCAGCCT[C/T]AAATTTCCAATTCAT | 10277 |
rs747217965 | snp | C/G | 1.64901e-05 | 0.00287137 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095453 | TCCTTCCTGTGTTTT[C/G]TGTTTAGGAGTAGCC | 10277 |
rs747249052 | snp | A/T | 1.74218e-05 | 0.00295137 | intron-variant | UBE4B | GRCh38.p7 | 1:10132513 | ACTGCTTTTCGCTGT[A/T]TGTCAAATTCATTCA | 10277 |
rs747277362 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059642 | AAGCGTGGCTGCTTA[C/G]GGCAAGGCCGAGGCG | 10277 |
rs747285179 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112702 | TAAATTTATGCATGT[A/G]CTATATTCCGCTTTC | 10277 |
rs747287073 | snp | A/C | 1.65072e-05 | 0.00287286 | intron-variant | UBE4B | GRCh38.p7 | 1:10119492 | TTTCTTGTCGTCCTC[A/C]CTTCCACCTTTCCTT | 10277 |
rs747336111 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140580 | GTTTCTTTATCCTCC[A/G]ATGGATTACCTCCTG | 10277 |
rs747396842 | in-del | -/T | 1.65434e-05 | 0.00287601 | intron-variant | UBE4B | GRCh38.p7 | 1:10161134 | TACAATATAATTGCC[-/T]TTTCCAGCTCCGGGA | 10277 |
rs747397550 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046033 | GCCCAGGTGCCTTCT[C/G]TCTTGTACCTACTTT | 10277 |
rs747401645 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137101 | TTCTGAGCCGAAATT[C/T]CCTACGGAGTGCTTC | 10277 |
rs747439945 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136182 | GAACATCACCAAAGA[C/T]TGTTGATGGGCTGGG | 10277 |
rs747455511 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | UBE4B | GRCh38.p7 | 1:10126892 | GGTAAAACTTTGTTC[C/T]TTTTCTTTAACTCAT | 10277 |
rs747501078 | snp | C/G | 1.6596e-05 | 0.00288058 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171359 | TTGGTCTCTCTGTGA[C/G]TTTACTGGCAGATTT | 10277 |
rs747506937 | snp | A/G/T | 9.88511e-05 | 0.00702975 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147089 | GACCCCGCATATCCC[A/G/T]AGTGAGTGTGCTTCT | 10277 |
rs747532941 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117973 | ACTGTGCCAGGTCGA[C/T]ATTAGCTTGTATCCT | 10277 |
rs747568900 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110361 | AAGAACTGCTTTTTG[C/T]GCGAGTGGCATAAAT | 10277 |
rs747611188 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073131 | TAATGTTTCCTCTGT[A/G]TGTCTCTGAGAAGCT | 10277 |
rs747617969 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058711 | GAAGCACTTCAGCGG[C/G]TGGTGTGACACTGAC | 10277 |
rs747636753 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175837 | TTCTTCTTTAATGAG[G/T]TAAGATTAATATATA | 10277 |
rs747646175 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175495 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCAGG | 10277 |
rs747646966 | snp | G/T | 1.70179e-05 | 0.00291696 | intron-variant | UBE4B | GRCh38.p7 | 1:10033721 | GGGGGACACCTTGAG[G/T]GATTAGTTGGCAACT | 10277 |
rs747662699 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075007 | ATCAAGCTTTGCTGT[G/T]GCCTCACATTTTATC | 10277 |
rs747692525 | snp | A/G | 3.31279e-05 | 0.00406975 | intron-variant | UBE4B | GRCh38.p7 | 1:10130469 | ACCGGCCTGTTCAGC[A/G]GCTTGACTGGCTCTT | 10277 |
rs747724260 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162469 | TGAGCCATTGCACCC[A/G]GACAATTTTTGTATT | 10277 |
rs747734048 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147775 | GAGAGTGAGCTAAGA[A/C]CATTGTTGATCACTT | 10277 |
rs747737061 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130138 | GAGCGCAGTGGCGCA[A/G]TCTCAGCTCACTGCA | 10277 |
rs747743981 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130563 | GGGCGGGAGCTGCAG[A/G]GACTCTCTTACTTAG | 10277 |
rs747764938 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075936 | GTAGTCCCAGTTACT[C/T]GGGAGGCTGAGGTGG | 10277 |
rs747780591 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142755 | CTGAAAGCTGCCTAC[A/G]TTCCTCTGCTCCTTA | 10277 |
rs747789990 | in-del | -/TTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146621 | GAATTCAGACACTGA[-/TTGT]TTGGCTTTTTCCCAC | 10277 |
rs747791745 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171564 | CCGTGATTGCACCAC[A/C]ACACTCCAGAATGGG | 10277 |
rs747792086 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117334 | AGGGTGGATCTTGGC[C/T]GCATGGGTGTTTGTG | 10277 |
rs747798138 | snp | A/G | 1.67671e-05 | 0.00289539 | intron-variant | UBE4B | GRCh38.p7 | 1:10179406 | AGTTTGCTTTGCTTT[A/G]TCCCCGCAGACCCTC | 10277 |
rs747823244 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101109 | TTTTGTACTTTAAGC[A/G]TGTCCCAGGTGGATG | 10277 |
rs747849279 | snp | C/T | 1.66632e-05 | 0.0028864 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151554 | TTCCCTGATGAAGTT[C/T]TATACAGGTAGGTTG | 10277 |
rs747853558 | snp | C/G | 1.65201e-05 | 0.00287398 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179974 | CGTTCCGCCGCCCAC[C/G]CTCTGCTAGACACAG | 10277 |
rs747861054 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039053 | AGGCAGAGCAAGACT[C/G]CATCAAAAAAACAAA | 10277 |
rs747904089 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119596 | TTTAGTACTACAAGG[C/T]TCCCTAACACAGCCC | 10277 |
rs747942500 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031296 | CTTGGCCAGGCTGGT[C/T]TTAAACTCCGGACCT | 10277 |
rs747945744 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051739 | GGAGAAATGTTCTGC[A/G]TATCAGGACTAAAGA | 10277 |
rs747959358 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046221 | CTACTTGCTGGGAAG[A/G]CTGAGAAATAGTTTT | 10277 |
rs748024320 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141974 | TGCTCCTTTCCTTTA[A/T]CAACAGTCTTAGAAA | 10277 |
rs748033324 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105639 | AGCCAATTGCTGCAG[C/T]AGCACGGTCACCAGA | 10277 |
rs748050017 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122617 | CAGGTGAAAATGCAG[A/T]TATGTAGTGCTTAAA | 10277 |
rs748085832 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093455 | AGTCCTAGGAAGAGA[G/T]AAAATTTAGTTTCTT | 10277 |
rs748091668 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | UBE4B | GRCh38.p7 | 1:10137223 | ATGTGCCATGATACC[A/G]TGTCCTGGGATTGCC | 10277 |
rs748107003 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123936 | CTGCCACCACACCCA[A/G]CTAATTTTTTGTATT | 10277 |
rs748107505 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102154 | GTAGCCTCCTAGTGG[G/T]GCAGTGCTTTATTTT | 10277 |
rs748108497 | snp | C/G | 1.65187e-05 | 0.00287386 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168191 | AGCGTGTGTCCCGCT[C/G]TTACCTCGCCCTGGC | 10277 |
rs748127106 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091514 | CAGTGGTATGATTAT[A/C]GCCCACTGCAGCTTC | 10277 |
rs748131932 | in-del | -/AC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137771 | ACAGAAGTCACAGGA[-/AC]ACAGAAGCAAATATT | 10277 |
rs748141473 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111191 | TCTACAAGGCCCTGC[A/G]TCTCACGTACACTCC | 10277 |
rs748150535 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069735 | AGACAGGGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 10277 |
rs748206604 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163577 | GAGGCTGAGGCAGGA[-/T]TAATTGCTTGAACCC | 10277 |
rs748208469 | snp | C/T | 1.65814e-05 | 0.00287931 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106279 | CTTGCCTCACCTTCC[C/T]GTGCAGCCAGCCAGT | 10277 |
rs748210458 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055548 | GTTTCCAACTCCTGG[C/T]TTCAAGCCTTCCTCC | 10277 |
rs748216416 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063096 | AACATGGTGAAACCC[C/T]GTCTCTAATAAAAAT | 10277 |
rs748265271 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056680 | CAGAGAGATAACCCA[A/G]CTGGAAACAGGTGCA | 10277 |
rs748265292 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042351 | TAGTGGGAGGAGAGG[G/T]ATAAAAAACAAGCAT | 10277 |
rs748284132 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122251 | TGCATTGTTCAAATC[-/AT]GTGCCCATTTCAACG | 10277 |
rs748286353 | snp | C/T | 1.65751e-05 | 0.00287876 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171348 | AGTGAGTTGAGTTGG[C/T]CTCTCTGTGAGTTTA | 10277 |
rs748290880 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132170 | CTACCTCCCCCACTC[C/T]ATATTCTGCTTTCAT | 10277 |
rs748333178 | snp | A/G | 3.31675e-05 | 0.00407218 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106371 | CCAGCCTTCATCCCC[A/G]CGGTATCGCCCCTAC | 10277 |
rs748337796 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147079 | CCGCATCCTGGACCC[C/T]GCATATCCCGAGTGA | 10277 |
rs748360093 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157307 | ATTATAGGCGAGAGC[C/T]ACCACGCTCAGCCAT | 10277 |
rs748382950 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143859 | CCTCTGCCACAGCTT[C/T]AGCCAAAACCCCTCT | 10277 |
rs748422146 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081578 | TCCTGGCACGTGCCA[C/T]CATGCCTGGCTAATT | 10277 |
rs748429885 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130742 | GAAAAATACTTCTCA[A/G]GGCCTGCCATTACCC | 10277 |
rs748432785 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169530 | CTGGCCTCCCTTAAA[A/G]GTTTGCAAAGTGCAA | 10277 |
rs748483197 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080089 | GCTATGCATTGTAGA[-/T]TTTTTTTGGAGCATT | 10277 |
rs748527443 | snp | C/T | 5.00981e-05 | 0.00500465 | intron-variant | UBE4B | GRCh38.p7 | 1:10102900 | TATTGAAACACCTAA[C/T]TCATACCTCTTATTT | 10277 |
rs748532186 | snp | G/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158461 | ACATAGCTCACCATG[G/T]CACCTTTATGGAGGA | 10277 |
rs748532318 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033929 | GAGTGTTCTTTTAGG[C/G]TATGAACAAGAGGAG | 10277 |
rs748535001 | snp | C/T | 1.97389e-05 | 0.0031415 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135179 | GAATGACTGGCTGAC[C/T]GAACTCTGTGAGTAC | 10277 |
rs748553424 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149007 | GCATATGCACTGTCT[G/T]CATTATTCCCTGTTC | 10277 |
rs748556042 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083018 | GCTGCATAGTATTGC[A/T]TGGTGTATATGTACC | 10277 |
rs748584350 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125607 | ACATAGTATACTCCT[A/G]TTACAACTTGTTGGC | 10277 |
rs748586286 | in-del | -/AAAG | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180670 | TATTCTAAACAAAAT[-/AAAG]AAAATCCTGCTGCTC | 10277 |
rs748605410 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170854 | TGATACTTTTTTTAA[C/T]TAAAAGCATAAATGT | 10277 |
rs748606192 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137694 | CTCAAATTTCCAATT[C/T]ATTAGCACCATGGTT | 10277 |
rs748631901 | snp | C/T | 1.66924e-05 | 0.00288893 | intron-variant | UBE4B | GRCh38.p7 | 1:10122080 | GTGTTCAAGCAGGTA[C/T]GGTCGTATGAGTTTG | 10277 |
rs748646866 | snp | A/G | | | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107373 | GTCCAGTTTGGGTCC[A/G]GGTATCAGAGGAATG | 10277 |
rs748647031 | snp | C/T | 1.65419e-05 | 0.00287588 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171153 | GAGCTTGGACCCCGA[C/T]TGGCTGCAATGCTGA | 10277 |
rs748661352 | snp | C/G | 1.6528e-05 | 0.00287467 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126804 | TATAGATATTTATCC[C/G]CATTTTACAAGGCCT | 10277 |
rs748699738 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095007 | TAATCTTGAACTCCA[A/G]ACCTCAGGTGGTCCA | 10277 |
rs748719154 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061521 | TTCCCAAAGTGCTGG[C/T]ATTACAGGGGTGAGC | 10277 |
rs748727008 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105608 | AACCCATTTGCCAGT[C/G]TGACAGCCACATCAC | 10277 |
rs748745200 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137922 | ATCACTTACTAATTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs748754369 | in-del | -/A | 1.66874e-05 | 0.0028885 | intron-variant | UBE4B | GRCh38.p7 | 1:10158530 | TTTCTTGCAAATCGC[-/A]GGTAGGATTGCAGCT | 10277 |
rs748762077 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061640 | AGGGATCTCCTTGAA[A/G]ATCTTGAGGGAATTG | 10277 |
rs748764951 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109076 | TAGGAGGAATAAAAT[A/G]TACCAAGTGTATAAA | 10277 |
rs748781264 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180368 | TGCTGCTAAAGAATC[-/T]TTTTTTCCCCTCTCC | 10277 |
rs748813372 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062684 | TAGTGAGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 10277 |
rs748817488 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046861 | TAGACCGCGGACATT[C/G]CTCAGGCAGACTGTA | 10277 |
rs748823265 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162776 | GTTTTCAACCCTCAC[G/T]CCTCCCTCACTCCCC | 10277 |
rs748835102 | snp | A/T | 1.64838e-05 | 0.00287083 | intron-variant | UBE4B | GRCh38.p7 | 1:10129464 | GTAAGCACTCACCTG[A/T]TGGGCTTGCACATTT | 10277 |
rs748854436 | in-del | -/AAATA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136945 | AATAAATAAATAAAC[-/AAATA]AAAAGTATCTTTAAA | 10277 |
rs748867228 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150514 | TTATAGTTAATATAA[C/T]ATGCTACAGCCAGTA | 10277 |
rs748871519 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042120 | GTGGACTTTCATTCC[C/T]GTTTGTTATTGCTGA | 10277 |
rs748873159 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171813 | TTGAACCCAGGAGGC[A/C]GAGGTTTCAGTGAGC | 10277 |
rs748880322 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088261 | ATATTCTGTCTTGTA[A/C]ATATGAAGATCAAAG | 10277 |
rs748881096 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155084 | AGAGAGAGAGAGAGA[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs748887006 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048442 | ATGAGAATGGACAGA[-/T]TTTTACCTAGAGAGT | 10277 |
rs748898902 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151631 | CTAAAGCTAGTGGAC[A/G]ACGTTGCTCTAAGCC | 10277 |
rs748914883 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107483 | GCAGGATAGGGTCAA[A/G]TGAGGTGGGCTCCAG | 10277 |
rs748919699 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131810 | CAAAAAAAATTAGCT[A/G]GGCATGGTGGCGGGT | 10277 |
rs748937534 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075121 | AGTAAATATTTTTGG[C/G]TTTGGAGGCTGTGAG | 10277 |
rs748969458 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135213 | GTTCGTGACTCGGTC[A/G]TTAAAACACTGCCCT | 10277 |
rs748989597 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164244 | TATTTGGAAGGCTGA[A/G]GTGGGAGAATCACTT | 10277 |
rs749010304 | snp | C/T | 0.000166199 | 0.00911437 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178799 | AATCGACTACAGCGA[C/T]GCTCCTGATGAGTTC | 10277 |
rs749016945 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100764 | TCTCCATGTTGGTCA[A/G]GCTGATCTCGAACTC | 10277 |
rs749053336 | snp | C/T | 1.65872e-05 | 0.00287981 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117555 | GCTGAACTACCTCAT[C/T]GAGTGTTTCGACCGA | 10277 |
rs749077237 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174848 | GAGCTTTGGTGGGGC[A/T]GGGGGCGGTAAGTGC | 10277 |
rs749138275 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123260 | GCGTGGTGAAACCCG[A/G]TCTCTACTAAAAATG | 10277 |
rs749153864 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131170 | ATTAATATGTCTTCA[A/G]TTCTCAAACTTAAAG | 10277 |
rs749165083 | snp | C/T | 3.30901e-05 | 0.00406743 | intron-variant | UBE4B | GRCh38.p7 | 1:10119482 | GTATTGTTTGTTTCT[C/T]GTCGTCCTCACTTCC | 10277 |
rs749233193 | snp | C/G | 1.65195e-05 | 0.00287393 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179971 | AACCGTTCCGCCGCC[C/G]ACCCTCTGCTAGACA | 10277 |
rs749234800 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161214 | GCTCGATGAAAGTCT[A/G]GAGTCTCTGAAGCGA | 10277 |
rs749235102 | in-del | -/AAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163687 | AAATAAATAAATATT[-/AAAG]AGAGAGAGTCTTGCT | 10277 |
rs749240039 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052343 | TCCCAAAATGCTGGG[A/T]TTATAGGCATGAGCC | 10277 |
rs749244653 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096655 | TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAACC | 10277 |
rs749245778 | in-del | -/T/TAGG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126307 | CCGTCTCAATATAGA[-/T/TAGG]TAGATAGATAGATAG | 10277 |
rs749257807 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142924 | ACCCGCCTGGCCAAC[A/G]TGGTGAAACCCTTTT | 10277 |
rs749266089 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063443 | TCCAGGCCTGAAATC[C/T]AGATTATTCTTCTTC | 10277 |
rs749290044 | snp | A/G | 0.000338123 | 0.012998 | intron-variant | UBE4B | GRCh38.p7 | 1:10166245 | TTGACCCATTTCAGA[A/G]CCTGCAGTGCAGTAC | 10277 |
rs749292041 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137130 | TCTTTCTCACCCTGC[A/G]TGCTCACCACCTCTC | 10277 |
rs749309746 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037379 | TTGTTTGTTATTTAT[A/G]TAGTGTATTACAGTG | 10277 |
rs749317021 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067116 | CTAAAAATAAGAGGA[A/G]CAGTTTGGCCCATCC | 10277 |
rs749339016 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091795 | ATTTTAGTAGAAACA[C/G]GGTTTCACTATGTTG | 10277 |
rs749339951 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078133 | TCCCACCTCAGCCTC[C/T]GAGTAGCTGGGGTTA | 10277 |
rs749345459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044423 | CAACCTTTTTGGCAC[C/T]AGGGACTGGTTTCGT | 10277 |
rs749349715 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10121991 | CGTCCTTCCTAGTGC[C/T]GTATATGCTGTGTAG | 10277 |
rs749352827 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043512 | GCTCACTGCAAGCTC[C/T]GCCACCTGGGTTCAC | 10277 |
rs749385011 | snp | A/C | 1.65921e-05 | 0.00288024 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168232 | GTGGACATGTTCCAC[A/C]TCCTCACGAAGCAGG | 10277 |
rs749386309 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166081 | GGCCCCCCAGTATCC[C/T]TGCAGAATCTCCATC | 10277 |
rs749428059 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134737 | ATTCATGTTATTTTA[A/G]ATACTTTTTCTTGGC | 10277 |
rs749440881 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180758 | TAGGGGTGTAAGTGT[A/G]TCAGGACTTATGTGA | 10277 |
rs749467853 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115840 | CTGAACACTCTAGGC[-/AT]AATTAGATGCTTATG | 10277 |
rs749472630 | snp | A/T | 1.66529e-05 | 0.00288551 | intron-variant | UBE4B | GRCh38.p7 | 1:10126790 | TTTGTTTTTTTTCTT[A/T]TAGATATTTATCCCC | 10277 |
rs749475668 | snp | A/C | 1.7472e-05 | 0.00295562 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106200 | CAACTAATTTAGCCT[A/C]TATGAAAGTAGTCCG | 10277 |
rs749477702 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145082 | AGACCAGCCTCATAG[G/T]GATAATTTTCCCAAC | 10277 |
rs749503279 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048893 | TGTGGTGAGCTTATC[-/T]TTTTCTGTTTTAACT | 10277 |
rs749507865 | snp | G/T | 1.70909e-05 | 0.00292321 | intron-variant, downstream-variant-500B, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171113 | TCAACAGCATGAATT[G/T]TCCTATTATCCTGTG | 10277 |
rs749522425 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116239 | CAACCTCCTCCCACG[G/T]TCAAGTGATTCTTGT | 10277 |
rs749525437 | snp | A/C | 1.65875e-05 | 0.00287984 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106273 | CCGTCTCTTGCCTCA[A/C]CTTCCCGTGCAGCCA | 10277 |
rs749530560 | snp | C/T | 1.72415e-05 | 0.00293606 | intron-variant | UBE4B | GRCh38.p7 | 1:10072004 | TGATTAGTTATAGAA[C/T]GCCCTTTTCCCCTCA | 10277 |
rs749559881 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115616 | ATGTGTAGTTTTCCA[A/C]AGTCTAAGGACAATG | 10277 |
rs749562912 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | UBE4B | GRCh38.p7 | 1:10146926 | AGGGACTTAGCTACT[A/G]ACTGATCTTTGGGTG | 10277 |
rs749570416 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103781 | TACAGGCATGCGCCA[C/T]CACACCCAGCTAATT | 10277 |
rs749583188 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071126 | TGGTCAGGCTGTTCT[C/T]GAACTCCTGACCTCG | 10277 |
rs749610373 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128628 | GTGAACTCCTGCACT[A/C]GGCAGTGAGAACGCT | 10277 |
rs749615960 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084316 | CTTGAAAGCCTTCCT[C/T]GTCTCCTTATTTCCA | 10277 |
rs749616082 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069273 | AAATTAGTCAATTTT[A/G]TGTTCAGTGCATTTT | 10277 |
rs749630217 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087004 | GTACTTAGGTATGCT[-/A]AAAGTGGACAAGACC | 10277 |
rs749630439 | snp | C/T | 8.23662e-05 | 0.00641688 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095533 | CTAATAGCCTTGAAA[C/T]GCAATCTCAGTCTCT | 10277 |
rs749641898 | snp | C/T | 3.5979e-05 | 0.00424125 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106555 | AGTGCCACGAGCAGA[C/T]GCCCCTCCTCCCTGA | 10277 |
rs749657813 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176025 | GGCAACCACAAATCT[A/G]CTGTCTCTCTTTTCC | 10277 |
rs749676551 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161420 | TTTCCTTCCATGAAA[-/T]TCATATTGCAGGATT | 10277 |
rs749716022 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083807 | GCATGGGTACTTCCT[C/T]GAATTGGACTGGCCT | 10277 |
rs749727896 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158500 | GAGTATGGGGCCCCT[C/T]GTGTCACAACTTGCT | 10277 |
rs749754939 | snp | A/T | 1.64868e-05 | 0.00287109 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101073 | TGTGCGGATTTATAA[A/T]AGGTAAAAGGCTTGT | 10277 |
rs749773979 | snp | C/G | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171355 | TGAGTTGGTCTCTCT[C/G]TGAGTTTACTGGCAG | 10277 |
rs749787384 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096215 | TGAAATTTAAAAGTT[C/T]GGAATATTTCATACA | 10277 |
rs749811056 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097393 | ATATATCTAAACATC[A/C]AAAAGGGAGAATAGA | 10277 |
rs749818456 | snp | A/G | 1.65274e-05 | 0.00287462 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135005 | AGATGATAGATTGGT[A/G]TCTACAGATGGATTT | 10277 |
rs749821551 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057781 | GTATTTTGCTAGTAA[C/T]TGCTAGAAGTTGGCC | 10277 |
rs749837391 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136671 | ACGCCTGTAATCCCA[-/G]CACTTTGGGAGGCCA | 10277 |
rs749845974 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083096 | TCTTTGCTATTGTAA[A/G]TAGTGCTATCGTGTA | 10277 |
rs749879851 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082756 | CAACTCATCATCTAG[A/C]TTTTAAGCCTCTCAT | 10277 |
rs749882450 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110635 | TTGTTTCCTAGGAAG[C/T]TGATGACTAGAAAGA | 10277 |
rs749885610 | in-del | -/AAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080733 | TTATTCAGCCTTCAA[-/AAAG]AAAGAAATTCTGTCA | 10277 |
rs749891240 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043005 | TAAAGTCATTCATTC[-/T]TTTTTTTTTTTTTTA | 10277 |
rs749930786 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065221 | ATTTGAAAGTATGGA[A/G]AACCACTAAAGCAGA | 10277 |
rs749953298 | snp | A/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031142 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCACGATC | 10277 |
rs749953447 | in-del | -/CTCA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162771 | AGGTAGTTTTCAACC[-/CTCA]CTCCTCCCTCACTCC | 10277 |
rs749965455 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153272 | GCACTTTAGGAGGCC[A/G]AGGTGGGAGGATTGT | 10277 |
rs749971917 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112653 | GATCTGCCCCCCTCA[A/G]CCTCCCAAAGTGTAG | 10277 |
rs750027923 | snp | C/G | 1.66885e-05 | 0.00288859 | intron-variant | UBE4B | GRCh38.p7 | 1:10161325 | GGACAGCTTTGCAGG[C/G]CATCTGCCTCCACAC | 10277 |
rs750038320 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043926 | ATTCAGCAATGAAAG[C/G]AAGTGTTACTTTGTA | 10277 |
rs750047497 | snp | C/G | 3.37558e-05 | 0.00410814 | intron-variant | UBE4B | GRCh38.p7 | 1:10121927 | TCTGTAGTGAGTTGA[C/G]TTCATCACCGTCCCT | 10277 |
rs750100993 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177869 | TGTGAGGTAGATGTT[A/T]CTCTGCCCATTTTAC | 10277 |
rs750103368 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105580 | AATGATGTCCACTCA[A/G]ACCAGAGATGAAAAC | 10277 |
rs750107862 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122387 | ACAAGAATACCCAGA[A/G]ACGGCATAAGGCATG | 10277 |
rs750121990 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175923 | GCGTTGCACAGCCAC[C/G]ACCTCTACCTAGTTC | 10277 |
rs750141475 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077987 | CAGATGAATGCCACT[G/T]TTTTATAGTTAACAC | 10277 |
rs750177365 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041598 | CCTCGGCCTTCCAAA[-/GT]GCTGGGATTACAAGC | 10277 |
rs750179542 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058638 | GACCACAGTCAGTGC[-/TG]CATCCTGAGCCCACC | 10277 |
rs750209387 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070775 | ATATGTTAAAAGGAA[G/T]AAGTGGCAGATTGTA | 10277 |
rs750221432 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | UBE4B | GRCh38.p7 | 1:10129356 | ACAGTCAGTTTAAGA[C/T]GAAATGCATTTAAAT | 10277 |
rs750223583 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056433 | TCAGCAAATATTTAC[C/T]GAGTGCTCTCTGGGA | 10277 |
rs750229411 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091379 | TGTGTTTTTAGTCGC[A/C]ATATTTAATTCACAT | 10277 |
rs750229834 | snp | A/C | 1.6582e-05 | 0.00287936 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106368 | AAGCCAGCCTTCATC[A/C]CCGCGGTATCGCCCC | 10277 |
rs750242742 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105181 | ATTAATATACATCAG[C/T]GGTAACTCTCAATGA | 10277 |
rs750260003 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168891 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs750265310 | snp | C/T | 1.7072e-05 | 0.00292159 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178652 | TTTGCAGAGATCCTA[C/T]AGTAAGGAATTGTTT | 10277 |
rs750273842 | snp | A/G | 1.65124e-05 | 0.00287331 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178763 | AGTGGAGGAGATAGT[A/G]GCCAAGAACGCACGC | 10277 |
rs750274394 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146217 | AGCACTTTGAGAGGC[C/T]GAGGCAGGCAGATCA | 10277 |
rs750277008 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057900 | TTCCGGTGGCAGGGA[A/G]GCAAGCATGGGAGGC | 10277 |
rs750294584 | in-del | -/TAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147924 | TGAAGGCGTGGAAAA[-/TAT]TATTTAAAATATGTG | 10277 |
rs750295704 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156030 | GTGAGACTCCATCTC[-/AAAAAAAAAAAAA]AAGAAAGAAGGCAGC | 10277 |
rs750296736 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105008 | TCCTGAAAGCCACAT[A/G]GTGACTAGATGTTGG | 10277 |
rs750305019 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158220 | TGTCGTGCCCTACAT[G/T]CAAAAGAAGTGCAAA | 10277 |
rs750307034 | snp | A/G | 1.68083e-05 | 0.00289894 | intron-variant | UBE4B | GRCh38.p7 | 1:10149139 | CTTGTAGTTTGATGT[A/G]CCATAATTTCATTTA | 10277 |
rs750368776 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048178 | GAGGCAACTAGCTTT[-/T]CTACCACAGGGATAC | 10277 |
rs750380176 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116138 | ACATTCCTGATGTTC[C/T]CATACTTTTTTTCTT | 10277 |
rs750386577 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101653 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10277 |
rs750427487 | snp | A/C | 1.65378e-05 | 0.00287552 | intron-variant | UBE4B | GRCh38.p7 | 1:10130835 | GTTCAGAAAACAAAT[A/C]CAGAGGAAGTATCAA | 10277 |
rs750429672 | snp | C/T | 1.70968e-05 | 0.00292371 | intron-variant | UBE4B | GRCh38.p7 | 1:10149312 | TATTTTACATAGTTC[C/T]AATATGTTTTTATGC | 10277 |
rs750469987 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060532 | CTGACTTCCCCAGGA[G/T]AGCTGGTTCCAGAAG | 10277 |
rs750490354 | snp | C/G | 1.87898e-05 | 0.00306505 | intron-variant | UBE4B | GRCh38.p7 | 1:10106610 | ACAGGAGAGTTGCAT[C/G]TGTGTTTGCGGTGCA | 10277 |
rs750508423 | snp | A/G/T | 3.38571e-05 | 0.00411432 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10101219 | GCGATGAAGCCCTTG[A/G/T]TACAGGTAATAGAAA | 10277 |
rs750522887 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062123 | CCATGTTGGCCAGGA[C/T]GGTCTCGATTTCTTG | 10277 |
rs750546741 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095432 | ATTATTTCACATGGG[A/G]CTTCATCCTTCCTGT | 10277 |
rs750562672 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170668 | TGTTATTTGTATCTG[A/G]TAAGTACATAAGAAT | 10277 |
rs750564902 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151514 | TGATTGAGAACCATC[C/G]TCTCTCCACCAAGTT | 10277 |
rs750570776 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137260 | ACCACTTTTTCTCAG[C/G]GGCAGGCAATTCCAT | 10277 |
rs750602577 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117808 | CATTCTAATAGAGAC[A/G]GAGCCAAGGTTTGAA | 10277 |
rs750626552 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041641 | TGCCCGGCCACATTT[A/G]TAGCATTCTTACGGT | 10277 |
rs750662695 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106861 | TTTGGCCTTTTGTCC[C/T]GTTGCCAGTGGTAGT | 10277 |
rs750666933 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074553 | CAACTGCAGTCAGGC[A/G]AGGGTTCCCGTGGTT | 10277 |
rs750675191 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148811 | CAGGTATGGTGGCAC[A/G]TGCCTGTAATCTCAG | 10277 |
rs750685661 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149729 | TTTTTTTTTCAAATC[C/G]TTATTTGGTTTATCA | 10277 |
rs750688347 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119177 | TGAGCCACCGTGCCC[G/T]GCCCAGGCTAGTCTT | 10277 |
rs750689673 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118574 | CAATGGCACAATCTC[A/G]GCTCACCGCAACCTC | 10277 |
rs750689723 | in-del | -/TTC | 1.65087e-05 | 0.00287299 | intron-variant | UBE4B | GRCh38.p7 | 1:10105492 | ACTGTGTGTAACCTG[-/TTC]TTTGTTCTGCCTTTC | 10277 |
rs750699268 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089701 | GTTTTACTTTTGTAA[-/T]TTTTTTTTTTTTTTT | 10277 |
rs750740322 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105698 | AATCCAGGAACAAGC[C/T]CCATGTTCTGCAGCG | 10277 |
rs750754734 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087347 | GAAAAGTTATGAAGA[C/T]AGTATACAGGATTCC | 10277 |
rs750763404 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100391 | GTTATTCACAGGCAC[A/C]GTAATAGTGCATACA | 10277 |
rs750778532 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093093 | TACACATACTATACT[A/G]TACTACAGATACAGT | 10277 |
rs750788993 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052845 | GTTATTCACCGTTCT[A/G]CATTCTGGAGGCTGA | 10277 |
rs750804219 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038824 | AGTTGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 10277 |
rs750838333 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064625 | TCTCTATCACCTCGT[C/G]TCTTTGTCACTTCCT | 10277 |
rs750853419 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160826 | TGTGTGCCTGTAGTT[C/T]CAGCTACTTAGGAGG | 10277 |
rs750859365 | snp | A/G | 3.42161e-05 | 0.00413605 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033646 | GGATCTCTCCTTAAC[A/G]CCTTTCACCATTAAG | 10277 |
rs750861485 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040295 | TTTAATTTTTAGTAG[A/G]GACGGTGTTTCACCA | 10277 |
rs750874055 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033656 | TTAACGCCTTTCACC[A/G]TTAAGAGGAAAGCGA | 10277 |
rs750897247 | snp | C/T | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145019 | CGCGAAATGCTGAAG[C/T]GCTGTAAAACTCAGC | 10277 |
rs750928362 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094879 | CACTGCAACGTCTTC[C/T]TCCCAGATTCAAAGG | 10277 |
rs750948800 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111548 | TCATCCGCCTGGTTC[C/T]GTGCACTATTCCAGG | 10277 |
rs750958171 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142505 | GTGAAACCTCGTCAC[A/T]ACTAAAAATACAAAA | 10277 |
rs750958193 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130027 | TTCGAGTCCTTTGGT[A/G]GTATAAGAAGAGTTC | 10277 |
rs750995918 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113030 | TTAGTCCATTTGCAT[A/T]GCCATACAGAAAGGG | 10277 |
rs751005819 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | UBE4B | GRCh38.p7 | 1:10130681 | TCCCAAATGTGCATT[A/G]TATGTTGACTGCATT | 10277 |
rs751020140 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057491 | GCGTGATCATGACTC[A/T]CTGCAGCCCCAAACT | 10277 |
rs751064668 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072182 | TCAATGTCCACAACA[C/T]GACCCCAGCTACCTC | 10277 |
rs751066024 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053031 | AGGGGTTCCGCCCTC[A/T]GGACCTCATCACATC | 10277 |
rs751070276 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157533 | ACCTGTAATCCCAGC[A/C]CTTTGGGAGGCCAAG | 10277 |
rs751105313 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033188 | TGCCAGGACGGCTGT[A/G]GGGTCGCCTTACCTC | 10277 |
rs751105414 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067852 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTTGGACTA | 10277 |
rs751117714 | snp | C/T | 0.000118828 | 0.00770714 | intron-variant | UBE4B | GRCh38.p7 | 1:10072506 | TGAATTTGGTTCTGC[C/T]GATTTTATGAATTTG | 10277 |
rs751125840 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100584 | TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG | 10277 |
rs751195248 | snp | A/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031161 | AGTGGCACGATCTCG[A/G]CTCCTTGCAACTTCT | 10277 |
rs751199264 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168527 | CTTTGTGCTTAGACA[C/G]TACATTGGATTATTC | 10277 |
rs751211114 | snp | A/G | 6.6084e-05 | 0.00574784 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179960 | AGCGATCACTAAACC[A/G]TTCCGCCGCCCACCC | 10277 |
rs751261608 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058647 | CAGTGCTGCATCCTG[A/T]GCCCACCAGCTGCCG | 10277 |
rs751263911 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093254 | ACTTGGCCTTTAATT[A/G]TGATAGGTAAAATAA | 10277 |
rs751274733 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133410 | ATATATAAAGCTGTT[-/A]GAGTGGTGCCTGGTA | 10277 |
rs751284506 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059134 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 10277 |
rs751290269 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078854 | TTGTTTTTCTAAGAC[-/AA]AGTCAGGCTGGAGTA | 10277 |
rs751303677 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171374 | GTTTACTGGCAGATT[C/T]GGAGATAATAACCAC | 10277 |
rs751334763 | in-del | -/AT | 1.65707e-05 | 0.00287838 | intron-variant | UBE4B | GRCh38.p7 | 1:10145078 | TTATAGACCAGCCTC[-/AT]AGTGATAATTTTCCC | 10277 |
rs751374851 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044139 | CACCTGCCAGGTGCC[A/G]GGTTCAAGCGATTCT | 10277 |
rs751428356 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045488 | TTTTGTTGTGGTTTA[A/T]TGTGCCATATTTTGT | 10277 |
rs751462584 | snp | A/G | 0.000116004 | 0.00761504 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106350 | CTCTGGAACTGCTGC[A/G]GGAAGCCAGCCTTCA | 10277 |
rs751477663 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146345 | AAATCTCTGCCATTC[A/G]GGAGACTGAGGCAGG | 10277 |
rs751511397 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147043 | TCTGAATTTTTATGG[C/T]CTTCTCATTCAGCTG | 10277 |
rs751530849 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134618 | GCTAATATAGAATTA[A/C]TGGAATGACAGTGGT | 10277 |
rs751557146 | snp | A/G | 7.29341e-05 | 0.00603836 | intron-variant | UBE4B | GRCh38.p7 | 1:10178616 | CTGACGTACATTTAC[A/G]TCTCACATTGCCATT | 10277 |
rs751566433 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153020 | CGGTTGCTAGCTCTG[C/G]GGGTACGAGACAAAG | 10277 |
rs751609620 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070443 | TATCCAGTTAAAATT[-/AA]AAAAAAAAAAAAAAA | 10277 |
rs751610350 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058268 | AACATTTTTTGAGTT[G/T]GATAAGTAACCTGGA | 10277 |
rs751619199 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | UBE4B | GRCh38.p7 | 1:10130451 | TCATTACATTTTTAC[C/T]CCACCGGCCTGTTCA | 10277 |
rs751630828 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140014 | GTGTGAGCCACTGCA[C/T]CCGGCCCATTTTAAT | 10277 |
rs751682513 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048914 | TGTTTTAACTTTTCC[C/T]ATTCTCTGCTATAAT | 10277 |
rs751695840 | snp | C/T | 1.75897e-05 | 0.00296556 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106535 | CCCTACCACCCGCCT[C/T]ACCCAGTGCCACGAG | 10277 |
rs751708234 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149928 | AGGAGGATTGCTTGA[A/G]CCTAGTTCAAGACCA | 10277 |
rs751732151 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171653 | TTGGGAGGTCGAGGC[A/G]GGCAGATCAAGAGGT | 10277 |
rs751740587 | snp | C/T | 1.65466e-05 | 0.00287628 | intron-variant | UBE4B | GRCh38.p7 | 1:10095629 | TTCTAATATGCTCTT[C/T]TATTTAGGGAAAGAG | 10277 |
rs751763788 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant | UBE4B | GRCh38.p7 | 1:10178868 | TTGAGTTAACTGGAA[A/G]TCGATAACATTACAA | 10277 |
rs751763900 | snp | C/T | 3.43849e-05 | 0.00414624 | intron-variant | UBE4B | GRCh38.p7 | 1:10151292 | TCAGCAGTTTCTCAG[C/T]GGTCTCTTTCTTGCT | 10277 |
rs751764161 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108805 | GTGAAAGTGTCTTTT[G/T]CACGTAGATAAAATC | 10277 |
rs751767399 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10095702 | CCAGCTAGAGACCCA[A/T]GCCAGTCCTTAGCAA | 10277 |
rs751799095 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150863 | AGGCTCCATCTCAAG[-/A]AAAAAAAAAAAAAAT | 10277 |
rs751817356 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109358 | TTGTTCTTGTTCCTT[A/T]CTACTGTTTTTGCTG | 10277 |
rs751823884 | snp | G/T | 1.87096e-05 | 0.0030585 | intron-variant | UBE4B | GRCh38.p7 | 1:10106599 | GTATTTATCCCACAG[G/T]AGAGTTGCATGTGTG | 10277 |
rs751852474 | in-del | -/CTTCCTTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044556 | CCTTCCTTACTCTTC[-/CTTCCTTC]CTTCCTTCCTTCCTT | 10277 |
rs751861208 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138661 | CATGCCTTAGTGCCC[A/G]GGCTGTAATTTTTAG | 10277 |
rs751871548 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175417 | AGCACTTTGGGAGGC[CA/TG]AGGCGGGCGGATCAC | 10277 |
rs751886108 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151468 | ATGACCAACCCTGCT[A/G]TTCAGCCACGAACCC | 10277 |
rs751898541 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075942 | CCAGTTACTCGGGAG[A/G]CTGAGGTGGGACGAT | 10277 |
rs751900641 | snp | A/G | 1.65578e-05 | 0.00287726 | intron-variant | UBE4B | GRCh38.p7 | 1:10161298 | CCGGGTGAGGACGTG[A/G]TCCAGAGGCTTGGAC | 10277 |
rs751910813 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163600 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 10277 |
rs751926412 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074936 | ACACATCCAGCGCTT[C/T]ACCTGACATCTCTGC | 10277 |
rs751961761 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119555 | CTTCTGAGCAACATC[C/T]GCTCACAGTGCATAT | 10277 |
rs751968740 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162843 | CGTCCATGTGTACCA[A/G]TGTTTAGCTCCCATT | 10277 |
rs751983330 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061332 | TGATTTTGGCCCACT[A/G]CAACCTCCGTTTCCT | 10277 |
rs752003571 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137170 | TAGTTGCCGTCGCTA[C/T]ATCCGCAGACTCCGG | 10277 |
rs752009916 | snp | A/T | 8.23621e-05 | 0.00641672 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105554 | ATTGGCCAGATTTTA[A/T]TGGAAGTGCTAATGA | 10277 |
rs752033958 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054376 | GGCGAGGGGACACCA[C/G]ACTTCTACTCAATGA | 10277 |
rs752076984 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143562 | ATACTCTTCCCATCT[C/G]AAATCCATACCCTTA | 10277 |
rs752083771 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176574 | GTTTTTGTTTCTTAA[A/T]TACTCATCCTAGTGG | 10277 |
rs752109428 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101736 | GATGGTCTTGATCTA[C/T]TGACCTTATGATCCA | 10277 |
rs752124501 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10129399 | ATTTCTAGGCACTAG[C/G]TGAGCTCTGTGAAAC | 10277 |
rs752128760 | snp | A/G | 1.64887e-05 | 0.00287125 | intron-variant | UBE4B | GRCh38.p7 | 1:10137240 | GTCCTGGGATTGCCT[A/G]AGTTACCACTTTTTC | 10277 |
rs752132102 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162160 | CCTGCCACCACACCT[A/G]GCTAGTTTTTGTATT | 10277 |
rs752132367 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131594 | GTAACTGCCGGCTGG[A/G]CGTGTTGGCTAATGC | 10277 |
rs752164494 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089361 | ATGTCAGTCTGCTCT[A/G]TGAAATAGAATATGT | 10277 |
rs752178323 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087634 | GAAGATTATGTCACA[C/T]AGGTGAAGTGCCCTT | 10277 |
rs752179598 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054925 | CGAGTAGCTGGGATT[A/G]CAGGCATGCACCACC | 10277 |
rs752221234 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136670 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 10277 |
rs752231033 | in-del | -/AGAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045908 | GTTGATTGTTGTAAC[-/AGAG]AGACATGAAGTGGCA | 10277 |
rs752234797 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055952 | AAAACAAAACCAGAA[A/G]TAGAAGTAGTAGATG | 10277 |
rs752234937 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041972 | AGTTGTGGGATTACA[A/G]GCATGATGCTGGAGT | 10277 |
rs752241237 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072115 | CAGAGGGAGAACCCT[C/T]CGGGGCCTCCCATAG | 10277 |
rs752336416 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147008 | GCTGGCCTACTTGAC[A/G]AGAGCTTCCTGAGAA | 10277 |
rs752341110 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126118 | AGCGTGGCCAACAAA[C/G]TGAAACCCCGTCTCT | 10277 |
rs752350087 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034337 | AATCTTTCAAACTTG[C/T]GTTTTGCTGTAGCAG | 10277 |
rs752390469 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033364 | GCCTAGCTGGGTAAC[C/T]TGGGAAGCAGAGGGT | 10277 |
rs752417919 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078842 | CAGGTTTCATTTTTG[-/T]TTTTCTAAGACAAAG | 10277 |
rs752419508 | snp | C/G/T | 3.32519e-05 | 0.00407736 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106430 | GCGTCTCCATTCTGT[C/G/T]GAGCTCCCCAAGTCC | 10277 |
rs752420198 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046508 | GGAGTAATACTCTGC[G/T]CTGGTCCATAGCCAT | 10277 |
rs752453452 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175379 | AAAAATAGCCGGGTG[C/T]AGTGGCTCACGCCTG | 10277 |
rs752483156 | in-del | -/AAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159685 | GTGAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 10277 |
rs752520045 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060499 | TGTCGTTATGCAGCC[C/G]ATGACTGTATTTCCT | 10277 |
rs752526141 | snp | C/G | 1.66211e-05 | 0.00288275 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135106 | ATATTTTTCACCCAA[C/G]ATGTCGGATTACTCT | 10277 |
rs752536400 | in-del | -/TTC | 1.65149e-05 | 0.00287353 | intron-variant | UBE4B | GRCh38.p7 | 1:10117438 | GATAAGAATCAGAAT[-/TTC]TTCTTGTCTTCTCTG | 10277 |
rs752539704 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173497 | AAAAAAAAAAAAATT[A/T]TATATATATATACAC | 10277 |
rs752575832 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169919 | ACTTGGGAAGCTGTG[A/G]CAGGAGAATCACTTG | 10277 |
rs752578791 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033455 | CAGGGAACAAGCGGC[G/T]GTAGTAGTCTGTGGG | 10277 |
rs752593191 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040122 | GAAAGCACATGTTTC[-/T]TTTTTTTTTTTTCGT | 10277 |
rs752607459 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154980 | TTTTTCTACAGTAAA[A/C]ATGTATTGTTAGTAG | 10277 |
rs752612367 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045810 | CATTTTGTGGGTAGA[A/G]CCAATAGGATTGGGT | 10277 |
rs752653327 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135618 | GCACGCACCTGTAAT[C/G]CCAGCTACTCAGGAG | 10277 |
rs752668888 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106758 | CCATGCTTCTGCCAG[A/G]CTCTAATCATGCTGG | 10277 |
rs752692119 | in-del | -/GG | 1.64904e-05 | 0.00287139 | intron-variant | UBE4B | GRCh38.p7 | 1:10137244 | GGGATTGCCTGAGTT[-/GG]ACCACTTTTTCTCAG | 10277 |
rs752695710 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128490 | TGGAATCAGCTGGGG[A/T]TCTTTAAAGGTGTTT | 10277 |
rs752701951 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037201 | CCCGGCTAATTTTGT[A/G]TTTTTAGTAGCGACG | 10277 |
rs752749908 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085436 | AAAGAGACTAGTTCA[A/G]CCCTGACCTGAGGGG | 10277 |
rs752758580 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129687 | AATCTCACTCTGTCA[C/G]CCAGGCTGGATGGAG | 10277 |
rs752792039 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049144 | GGCAAATATTTCAGA[G/T]TAGGAGACTTGAATA | 10277 |
rs752796352 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096201 | CTTTTACTAATTAGT[A/G]AAATTTAAAAGTTTG | 10277 |
rs752797981 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171796 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 10277 |
rs752799998 | snp | A/G | 1.65666e-05 | 0.00287802 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178700 | GATGCGGAAGGCAGG[A/G]ATCAAATCCACAATA | 10277 |
rs752806766 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050628 | TTTATCCAAGTTCTG[A/G]CACAGGGCTTGGCAC | 10277 |
rs752810182 | snp | C/G | 1.64827e-05 | 0.00287073 | intron-variant | UBE4B | GRCh38.p7 | 1:10129376 | TGCATTTAAATGACT[C/G]TGATCTTATTTCTAG | 10277 |
rs752829470 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070909 | GAATTAAATTGGCTA[C/T]TTATTCATTAATTTA | 10277 |
rs752832776 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140156 | TCCCTCATTTTTGTT[A/G]TATCATATCTTATTA | 10277 |
rs752842115 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154787 | GCAGAGGTTGCAGTG[A/T]GCCAAGATCGTGCCA | 10277 |
rs752861979 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038548 | AGCGACCTGGCTTAG[A/C]AGTGATGGGGTTGGA | 10277 |
rs752886293 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125080 | GCATTTAGCTGAGAT[C/T]GCGCCACTGCACTCC | 10277 |
rs752910546 | in-del | -/AAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159688 | GACTCCGTCTCAAAT[-/AAAT]AAATAAATAAATAAA | 10277 |
rs752926705 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084215 | AGGGGCAAATACTGT[G/T]TGTGAGAGTGATTTC | 10277 |
rs752955827 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060079 | GTCGTCAGGTCCCTG[-/TG]TGTGTGTGTGGAGGG | 10277 |
rs752975297 | snp | C/T | 1.66671e-05 | 0.00288674 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106453 | CCAAGTCCCCCTGCC[C/T]TCGCCAGTAGCCCCC | 10277 |
rs752979773 | snp | G/T | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117476 | TGGGAGCCTCTGGTG[G/T]AGCAAGTAATTGGGA | 10277 |
rs752986810 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172421 | GGAAAGAGGCACAGA[A/G]AGGTTAAATAGCTTG | 10277 |
rs752988867 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141232 | TTGATTAAAGGGACT[G/T]TGCAGCTGTGATATC | 10277 |
rs752995596 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128363 | ACACAGTGAGTGAGA[A/G]GGTACAATAATGAGA | 10277 |
rs753016916 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110395 | TGAAGTGAGAATTAC[C/T]GTGTGTGAAAAGATA | 10277 |
rs753061950 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151834 | CCAGGGTATCAAGAG[C/T]ACAAGTTGGTAGTGT | 10277 |
rs753065709 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142449 | GCCGAGGTGGGCAGA[C/T]CACATGAGGTCAGGA | 10277 |
rs753092149 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062598 | GCTGCAGGCGTAAGC[C/T]GCTGTACCGGCCGCC | 10277 |
rs753104124 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071035 | ATTCTCCTGCCTCAG[C/T]AGCTGGGATTACAGG | 10277 |
rs753104193 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039097 | ACACACACAGAAAAA[A/C]AAACAAAAAAGCAAT | 10277 |
rs753106906 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102997 | AGGCCTTACAGCTGG[G/T]CTGTAAGATCTTCCG | 10277 |
rs753132133 | snp | C/T | 1.65434e-05 | 0.00287601 | intron-variant | UBE4B | GRCh38.p7 | 1:10161134 | GTACAATATAATTGC[C/T]TTTCCAGCTCCGGGA | 10277 |
rs753144500 | snp | C/T | 3.32094e-05 | 0.00407475 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178796 | AGAAATCGACTACAG[C/T]GACGCTCCTGATGAG | 10277 |
rs753144666 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042681 | AACAAACATGTTCAC[A/G]TAAGGTGTCATTTGA | 10277 |
rs753210618 | snp | A/T | 8.56201e-05 | 0.00654238 | intron-variant | UBE4B | GRCh38.p7 | 1:10117623 | GAAATGGATTAACTT[A/T]AAAAAAAAAAAGCCT | 10277 |
rs753222347 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115930 | AAATATGGCATTATA[A/G]CCTTGTGGGACCACT | 10277 |
rs753252439 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150311 | TGTTGAAAAACCAAC[C/T]TTGGAATTTAAGCAA | 10277 |
rs753253235 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132601 | ATTGAACAAGGTAGA[A/C]GAGCTTCCTGCTTTT | 10277 |
rs753259261 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161285 | GGGACCAGTTGCCCC[A/G]GGTGAGGACGTGGTC | 10277 |
rs753264704 | snp | A/T | 8.37977e-05 | 0.00647239 | intron-variant | UBE4B | GRCh38.p7 | 1:10103113 | AATCTAGCTCAGCAG[A/T]CTTACTGCAGAGTAC | 10277 |
rs753292831 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077829 | TACATGATAACATAA[C/T]TAGTGCCTATGGAAC | 10277 |
rs753299212 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121084 | GAAACATATAATACG[A/G]CCAGGCGTGGTGGCT | 10277 |
rs753322853 | snp | A/G | 6.71817e-05 | 0.00579537 | intron-variant | UBE4B | GRCh38.p7 | 1:10121937 | GTTGACTTCATCACC[A/G]TCCCTAATGTTCATG | 10277 |
rs753329446 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043761 | AGATGGTGTAATCAC[C/G]GTTGGCCAGGTGGCA | 10277 |
rs753334994 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042868 | GGGAAGAATGTTCCC[A/G]GGTAAAGGGAACAGC | 10277 |
rs753340710 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121262 | TTGGGAGGCTGAGCA[A/G]GAGAATCACTTGAAC | 10277 |
rs753347864 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139878 | GGATTACAGGCATGT[A/G]CCACCACGCCCAGCT | 10277 |
rs753434706 | snp | C/G | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168185 | AGGATGAGCGTGTGT[C/G]CCGCTCTTACCTCGC | 10277 |
rs753449921 | snp | A/G | 1.67245e-05 | 0.00289171 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106238 | CTCCCAGTTTCTGGA[A/G]CTCTGTTCCCGTGAT | 10277 |
rs753462263 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146083 | TCTTCAAGATGCACA[A/G]TTAACAAGGGGCCCT | 10277 |
rs753464811 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056179 | TGTTTGGCAGTTTTA[A/G]GCTCTTGATCTTTTT | 10277 |
rs753477883 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081979 | CTTGGCCTCCCAATG[G/T]GTTGGGACTACAGGC | 10277 |
rs753503629 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144462 | AAAATATGGCCCGAC[A/G]CAGTGGCTCATGCCT | 10277 |
rs753509081 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062957 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 10277 |
rs753534877 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141030 | TAATCATGTCAGTGA[-/T]TTTTAGCCCTACATA | 10277 |
rs753542673 | snp | A/G | 1.69183e-05 | 0.00290841 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033684 | CGATGGAGGAGCTGA[A/G]CGCTGATGAGGTGAG | 10277 |
rs753553997 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068570 | TAGTCGGGCTGGTCT[C/T]GAACTCCTGACCTCG | 10277 |
rs753557685 | in-del | -/AAACAAGGCTGGGC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143117 | TCTCAAAAAAGCAAA[-/AAACAAGGCTGGGC]ACGTGTCTGACACCT | 10277 |
rs753560661 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115302 | AATATCATAGTCGCT[C/G]TCTTGCCCAGGCTGG | 10277 |
rs753571265 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034593 | CTTTCAGGACCCCTA[C/T]TGGCCATACCCTCTT | 10277 |
rs753572020 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089947 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 10277 |
rs753597734 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055224 | TTTTAATGAATGCCA[A/G]TTGGAACAAATGCTT | 10277 |
rs753600433 | snp | C/T | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145029 | TGAAGCGCTGTAAAA[C/T]TCAGCTTAAGGTTTG | 10277 |
rs753636768 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143661 | TGCGACAAGTTTGGA[A/G]GAGCCATTCTTTTGT | 10277 |
rs753662515 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083783 | TTGGAACAGGTGTGT[C/T]CTATGCTGGCATGGG | 10277 |
rs753668938 | snp | C/G/T | 5.23047e-05 | 0.00511372 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106530 | TCCACCCCTACCACC[C/G/T]GCCTCACCCAGTGCC | 10277 |
rs753712047 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158069 | GTGGGGGGAGTATGA[C/T]AATTCAGCTTTTGGT | 10277 |
rs753712879 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10170292 | GACTCTTTTATTTCA[C/T]AGCTTCTCAACAGTG | 10277 |
rs753716618 | snp | C/T | 3.46855e-05 | 0.00416432 | intron-variant | UBE4B | GRCh38.p7 | 1:10132507 | CTACAGACTGCTTTT[C/T]GCTGTTTGTCAAATT | 10277 |
rs753727609 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156862 | CAAAAAAATGTGTTC[G/T]TTGGAAAATACAGAA | 10277 |
rs753730258 | snp | A/C/G | 3.30002e-05 | 0.00406192 | intron-variant | UBE4B | GRCh38.p7 | 1:10095608 | AAAGGTAAAATGAAG[A/C/G]CAGTTTTCTAATATG | 10277 |
rs753740101 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126397 | TGAATTTTTTAACAG[G/T]TTATAGATGCTTGGT | 10277 |
rs753782440 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096606 | AGGCGCCTGTAATCT[C/T]AGCTACTGGGGAGGC | 10277 |
rs753834283 | snp | C/T | 3.32447e-05 | 0.00407691 | intron-variant | UBE4B | GRCh38.p7 | 1:10161118 | GGAGATGTATGACCA[C/T]GTACAATATAATTGC | 10277 |
rs753839442 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119580 | GCATATCCCATACTG[C/T]TTTAGTACTACAAGG | 10277 |
rs753839477 | snp | A/C | 2.13641e-05 | 0.00326827 | intron-variant | UBE4B | GRCh38.p7 | 1:10134958 | TTTTTTTTAATGTTT[A/C]AAAATACTTTTTCTT | 10277 |
rs753892868 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072499 | TTAAGACTGAATTTG[A/G]TTCTGCTGATTTTAT | 10277 |
rs753903083 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102984 | GTGTCTGAAGAGCAG[A/G]CCTTACAGCTGGTCT | 10277 |
rs753904475 | in-del | -/CACACAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166966 | ACACACACACACACA[-/CACACAAA]AAAAAAAAATTAGCT | 10277 |
rs753923979 | snp | C/T | 1.73927e-05 | 0.0029489 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135151 | CGCGTGTGAATGCAA[C/T]GATGGAAGATGTGAA | 10277 |
rs753934925 | in-del | -/GAA | 0.000484379 | 0.0155549 | intron-variant, cds-indel | UBE4B | GRCh38.p7 | 1:10107288 | AGTGATGAAGAAGAT[-/GAA]GAAGAAGAAGATGAT | 10277 |
rs753947332 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038767 | ACTGGTCCTCCCACT[C/G]CCAATTTTTTTTTTA | 10277 |
rs753950716 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040011 | GTGAAGGAGGGGAGG[C/G]GAGGAGAGATGGAGA | 10277 |
rs753952392 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074264 | TTGGACCCTAGATCC[C/T]ATCTCCCTTCAGTTA | 10277 |
rs753953687 | in-del | -/TTC | 2.35092e-05 | 0.00342842 | intron-variant | UBE4B | GRCh38.p7 | 1:10132343 | ATAGTTTTAATTTGT[-/TTC]TTCTTTTTAAAAATA | 10277 |
rs753959731 | snp | A/T | 1.6516e-05 | 0.00287362 | intron-variant | UBE4B | GRCh38.p7 | 1:10137032 | ATTGAGACATGTAAT[A/T]GATTTTATTTAGGGA | 10277 |
rs753962500 | snp | C/T | 1.66879e-05 | 0.00288855 | intron-variant | UBE4B | GRCh38.p7 | 1:10103101 | AAAGAAGGTAGGAAT[C/T]TAGCTCAGCAGTCTT | 10277 |
rs753983837 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059389 | GTCAGAGCTCTGCCC[G/T]TTTGGAATGAAGAAA | 10277 |
rs754029397 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117019 | ATGAGGGCTTTTGAG[A/T]TCCATGGTAGAAGTC | 10277 |
rs754041737 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071373 | GATCACTTGGGGCCA[C/G]GAGGTTGAGACCAGC | 10277 |
rs754109308 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111429 | GACAGCTGTATGGCC[A/G]GCTCCCTCACTCTCC | 10277 |
rs754110173 | snp | C/T | 8.25784e-05 | 0.00642514 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171323 | GAAAGCCATTGCTGA[C/T]GACCAGGTCAGTGAG | 10277 |
rs754118135 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126872 | TACTTTAAATACCCC[C/T]TCATGGTAAAACTTT | 10277 |
rs754119546 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130525 | TGCGGTTGTGGTTGC[C/T]GAAATCCTTAAGTCC | 10277 |
rs754154046 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072083 | CCTCTCAGCCAACCA[C/T]CCCACTCACCTCTCC | 10277 |
rs754186357 | snp | C/T | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178776 | GTGGCCAAGAACGCA[C/T]GCGCAGAAATCGACT | 10277 |
rs754192634 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBE4B | GRCh38.p7 | 1:10098638 | TAGATTAAAGATGGA[A/G]TAAGGATGCTTCACT | 10277 |
rs754214824 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085701 | GAGAAACTGAGGTAG[C/T]AAGAACAAGTACAGA | 10277 |
rs754220300 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147001 | TGCTGATGCTGGCCT[A/G]CTTGACGAGAGCTTC | 10277 |
rs754229219 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044730 | GGGACCATAGGCGCA[C/T]GCCATCATGCCCGGC | 10277 |
rs754250259 | snp | C/T | 1.88219e-05 | 0.00306767 | intron-variant | UBE4B | GRCh38.p7 | 1:10106617 | AGTTGCATGTGTGTT[C/T]GCGGTGCAGGGAAAG | 10277 |
rs754280005 | snp | A/G | 4.95708e-05 | 0.00497825 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179516 | GCTCAACTCCCCCAC[A/G]GACCCCTTCAACCGG | 10277 |
rs754282198 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058653 | TGCATCCTGAGCCCA[C/G]CAGCTGCCGCCTGCA | 10277 |
rs754297312 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109767 | GCAATTCTCGTGCCT[C/T]AGCCTCCCAAGTAGC | 10277 |
rs754321379 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | UBE4B | GRCh38.p7 | 1:10130641 | GTGGCTACTTGTACT[C/T]TGCTGCCCTTTTATT | 10277 |
rs754322276 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147588 | TCCCTGTAATTAGTT[A/G]CAATAATAGGCAAAT | 10277 |
rs754372556 | snp | A/C | 4.95013e-05 | 0.00497475 | intron-variant | UBE4B | GRCh38.p7 | 1:10117448 | AGAATTTCTTCTTGT[A/C]TTCTCTGAAGTTTGG | 10277 |
rs754398928 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090307 | GTATTTTTCATAGAG[A/T]CGGGGTCTCCCTGTG | 10277 |
rs754427924 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078812 | TAGGTCTGCCTGTAT[A/G]CTCTCTAGAGCTGGC | 10277 |
rs754431540 | snp | A/G | 8.23716e-05 | 0.00641709 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158446 | AAAGCCTTTGGCAAA[A/G]CATAGCTCACCATGG | 10277 |
rs754441261 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058649 | GTGCTGCATCCTGAG[A/C]CCACCAGCTGCCGCC | 10277 |
rs754492212 | snp | C/T | 1.65187e-05 | 0.00287386 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168187 | GATGAGCGTGTGTCC[C/T]GCTCTTACCTCGCCC | 10277 |
rs754524224 | snp | A/G | 1.69873e-05 | 0.00291434 | intron-variant | UBE4B | GRCh38.p7 | 1:10033713 | AGGAGGTTGGGGGAC[A/G]CCTTGAGGGATTAGT | 10277 |
rs754531698 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089948 | GATCCGCCCACCTCG[C/G]CCTCCCAAAGTGCTG | 10277 |
rs754558866 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080747 | AAAAGAAAGAAATTC[C/T]GTCATTTGTGGCAAC | 10277 |
rs754563150 | snp | A/C | 1.6649e-05 | 0.00288518 | intron-variant | UBE4B | GRCh38.p7 | 1:10130466 | CCCACCGGCCTGTTC[A/C]GCGGCTTGACTGGCT | 10277 |
rs754564252 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057603 | TAGAGATGGAGTCTT[A/G]CTGTGTTCCCCAGGC | 10277 |
rs754571104 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102179 | TATTTTGTATAGTTC[C/T]TTAATGTTTACAAAA | 10277 |
rs754587739 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100069 | GTCTTGGCTCACTGC[A/G]AGCTCTGCCTCCCGG | 10277 |
rs754588350 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086847 | GGCATGTGCCACCAC[A/G]CCCGGCTAATTTTTG | 10277 |
rs754600280 | snp | A/C/G | 4.3883e-05 | 0.00468401 | intron-variant | UBE4B | GRCh38.p7 | 1:10144922 | TTCTTTCATTTGACT[A/C/G]TTAGTCTTTGATTTC | 10277 |
rs754627068 | in-del | -/TCTCTCTGTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111001 | ACCCTGTCCCTCTCT[-/TCTCTCTGTC]TCTCTCTGTCTCTCT | 10277 |
rs754661490 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136616 | TTTAAGTTTATAATT[A/G]CAAAAGTATCCTTAA | 10277 |
rs754741794 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079481 | TTTACTTTTAAATGT[A/G]TATAATAAAATAGGA | 10277 |
rs754754743 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135606 | GCGGGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 10277 |
rs754768060 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045627 | AACAGAAATCTCTGC[C/T]CTCCTGGGCATTCTG | 10277 |
rs754807030 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167483 | TAATAATGACTAAGT[A/G]AAAGTTATTATTAAG | 10277 |
rs754811835 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123678 | TGTTTTTTGTTTGTT[A/T]GTTTCCCCATCACCA | 10277 |
rs754825047 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168663 | TTTGGGAGCCCAAGG[C/T]GGGCAGATCACGAGG | 10277 |
rs754849000 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091638 | TAAGATGGAGTATTG[C/T]TGTGTCACCCAGGCC | 10277 |
rs754849857 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153455 | TGATCTTGCTGCTGC[A/G]TTCCAGCCTGTGAAA | 10277 |
rs754879116 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147217 | ACTTCTCTGCAAGGC[A/G]CAGTGGTTCACGCCT | 10277 |
rs754880459 | in-del | -/TTAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070754 | ATAAGATGTTGCTCT[-/TTAA]TTATATGTTAAAAGG | 10277 |
rs754916747 | in-del | -/GAA | 0.000484379 | 0.0155549 | intron-variant, cds-indel | UBE4B | GRCh38.p7 | 1:10107289 | AGTGATGAAGAAGAT[-/GAA]GAAGAAGATGATGAT | 10277 |
rs754926667 | snp | A/C | 2.10334e-05 | 0.00324288 | intron-variant | UBE4B | GRCh38.p7 | 1:10134959 | TTTTTTTAATGTTTA[A/C]AAATACTTTTTCTTT | 10277 |
rs754935327 | in-del | -/A | 1.70327e-05 | 0.00291823 | intron-variant | UBE4B | GRCh38.p7 | 1:10033713 | AGGAGGTTGGGGGAC[-/A]CCTTGAGGGATTAGT | 10277 |
rs754945782 | snp | A/C | 1.67728e-05 | 0.00289588 | intron-variant | UBE4B | GRCh38.p7 | 1:10121940 | GACTTCATCACCGTC[A/C]CTAATGTTCATGGGT | 10277 |
rs754972364 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172839 | CGATGCTGGACCACA[A/G]AGACCATGTGGCCCC | 10277 |
rs754974888 | snp | G/T | 5.24269e-05 | 0.00511964 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135152 | GCGTGTGAATGCAAC[G/T]ATGGAAGATGTGAAT | 10277 |
rs754986006 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105617 | GCCAGTCTGACAGCC[A/G]CATCACAGCCAATTG | 10277 |
rs754994555 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059174 | GGTGGAGCTTGTGGT[A/G]AGCCAAGATTGCGCC | 10277 |
rs755003948 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044214 | GCGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 10277 |
rs755006575 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148479 | TCTACTAAAAATACA[A/T]AAATTAGCCAGGTGT | 10277 |
rs755013295 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034817 | TAGGAAAGGAAGCAA[A/T]TGATTTTGTTGATTG | 10277 |
rs755023133 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124847 | ATATATAGGTCAGGC[A/C]AGGCATGGTGGCTCA | 10277 |
rs755033302 | snp | G/T | 3.32237e-05 | 0.00407563 | intron-variant | UBE4B | GRCh38.p7 | 1:10161120 | AGATGTATGACCATG[G/T]ACAATATAATTGCCT | 10277 |
rs755048729 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115470 | GAGATAGGGTTTCAC[A/C]ATGTTGGTCAGGCTG | 10277 |
rs755048844 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093155 | TTTATAACTTGTTTT[G/T]TAGGGTAGAAATTTT | 10277 |
rs755052017 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037120 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTT | 10277 |
rs755056386 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158250 | AATTTCACCAGCTCT[C/G]TGATTTTGCAGGTTT | 10277 |
rs755088325 | snp | C/T | 1.64895e-05 | 0.00287132 | intron-variant | UBE4B | GRCh38.p7 | 1:10137049 | ATTTTATTTAGGGAA[C/T]GATGTTATTTTTCCT | 10277 |
rs755122750 | snp | A/G | 3.31824e-05 | 0.00407309 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126794 | TTTTTTTTCTTATAG[A/G]TATTTATCCCCATTT | 10277 |
rs755151484 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128344 | TGCTTGCATAATAAC[A/G]AGGACACAGTGAGTG | 10277 |
rs755168574 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109395 | GTCTGTGCATCTACT[C/T]GGTTCCTTTGGCAGG | 10277 |
rs755198924 | snp | A/G | 1.65496e-05 | 0.00287655 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171337 | ACGACCAGGTCAGTG[A/G]GTTGAGTTGGTCTCT | 10277 |
rs755200981 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10095845 | GGTGCGATCATGGCT[C/T]ACTGCAATTTCCGCC | 10277 |
rs755210795 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062372 | GGCTGGAGTGCCATG[A/G]CACGATCCTGGCTCA | 10277 |
rs755228201 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061335 | TTTTGGCCCACTACA[A/C]CCTCCGTTTCCTGGG | 10277 |
rs755237157 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126873 | ACTTTAAATACCCCC[C/T]CATGGTAAAACTTTG | 10277 |
rs755258250 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082882 | TCTCATTGTTCAACT[C/T]CCATTTATGAGTGAG | 10277 |
rs755270435 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170490 | GTTTCAGGTTTGCTT[A/G]AAACCATGTATGCCC | 10277 |
rs755272788 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142390 | CAGGAGTCCTAAAAT[A/C]GGCCCAGCGCAGTGG | 10277 |
rs755280984 | snp | A/G | 1.68162e-05 | 0.00289962 | intron-variant | UBE4B | GRCh38.p7 | 1:10179389 | GGCTCTCAGTAGATT[A/G]GAGTTTGCTTTGCTT | 10277 |
rs755292165 | snp | A/C/T | 8.29093e-05 | 0.00643809 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106370 | GCCAGCCTTCATCCC[A/C/T]GCGGTATCGCCCCTA | 10277 |
rs755324771 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076012 | TCACACCACTGCATT[C/T]CAGCCTGGGCAACAG | 10277 |
rs755327612 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130531 | TGTGGTTGCCGAAAT[C/T]CTTAAGTCCTGGCTG | 10277 |
rs755360848 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140785 | GGGGTGTGTATATGC[A/G]TATTGGAAAGAGGAT | 10277 |
rs755390978 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149929 | GGAGGATTGCTTGAG[A/C]CTAGTTCAAGACCAG | 10277 |
rs755420565 | snp | G/T | 9.88647e-05 | 0.00703012 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158451 | CTTTGGCAAAACATA[G/T]CTCACCATGGCACCT | 10277 |
rs755439942 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082633 | TATTAAGAAGGCGAC[-/TT]TTTTTTTTTTTTTTT | 10277 |
rs755467109 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112705 | ATTTATGCATGTACT[A/G]TATTCCGCTTTCTCC | 10277 |
rs755483676 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041936 | CTGACCTCAAATGAT[C/T]CACCCACCTCAGCCT | 10277 |
rs755502122 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040464 | CCATGTTGCCCAGGC[A/T]GGTCTCAAACTCCTG | 10277 |
rs755520664 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039040 | ACTCTAGCCTGGGAG[A/G]CAGAGCAAGACTCCA | 10277 |
rs755529832 | snp | C/G | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102986 | GTCTGAAGAGCAGGC[C/G]TTACAGCTGGTCTGT | 10277 |
rs755560488 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057066 | ATTGGCCCGCCTCAG[C/G]CTTCCAAAATGCTGG | 10277 |
rs755572700 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041976 | GTGGGATTACAGGCA[C/T]GATGCTGGAGTGCAG | 10277 |
rs755584923 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033398 | AAGTGGCGCCTTAAG[A/T]CAACCCTGTAGCAGC | 10277 |
rs755602888 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119563 | CAACATCCGCTCACA[C/G]TGCATATCCCATACT | 10277 |
rs755623965 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164063 | AACAGAGTCTTGACC[A/G]GGCACAGTGGCTCAT | 10277 |
rs755627549 | snp | A/G | 0.000132082 | 0.00812548 | intron-variant | UBE4B | GRCh38.p7 | 1:10106620 | TGCATGTGTGTTTGC[A/G]GTGCAGGGAAAGGAG | 10277 |
rs755671569 | snp | A/G | 3.38203e-05 | 0.00411206 | intron-variant | UBE4B | GRCh38.p7 | 1:10103131 | TACTGCAGAGTACTC[A/G]ACAAGAAAATAAGAT | 10277 |
rs755700547 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137184 | ATATCCGCAGACTCC[A/G]GGCTATCCGGGAGCT | 10277 |
rs755710070 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089419 | TCTGAAGCAGGAGGA[A/T]CATTTGAGCCCAAGT | 10277 |
rs755718728 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105585 | TGTCCACTCAGACCA[C/G]AGATGAAAACCCATT | 10277 |
rs755727459 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132697 | AATCAGTGAAGAAAA[C/T]AGAGCAAAGTAAATG | 10277 |
rs755728662 | in-del | -/GACTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039960 | ACCAAAAATACCAAG[-/GACTGT]GATTAACCCAGTTTT | 10277 |
rs755746215 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075018 | CTGTTGCCTCACATT[A/T]TATCTTCTCCCAGGT | 10277 |
rs755754108 | snp | C/T | 1.66663e-05 | 0.00288667 | intron-variant | UBE4B | GRCh38.p7 | 1:10161328 | CAGCTTTGCAGGCCA[C/T]CTGCCTCCACACACG | 10277 |
rs755796163 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101746 | ATCTATTGACCTTAT[A/G]ATCCACCTGCCTTGG | 10277 |
rs755801970 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054964 | CTAATTTTTGTATTT[C/T]TAATAGAGATGGGGT | 10277 |
rs755809380 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168177 | GCTTGCTCAGGATGA[A/G]CGTGTGTCCCGCTCT | 10277 |
rs755819852 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075938 | AGTCCCAGTTACTCG[A/G]GAGGCTGAGGTGGGA | 10277 |
rs755838364 | in-del | -/TGGTGAAACCCGGTCTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123248 | CCAGCCTGGCCAGCG[-/TGGTGAAACCCGGTCTC]TACTAAAAATGCAAA | 10277 |
rs755886624 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156556 | TATTGCTACATAATA[A/C]ATTAACATTTACTTA | 10277 |
rs755897070 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033610 | ACTCTCCTTCCTCCC[G/T]CCGTGGTCTCGAGAA | 10277 |
rs755943198 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113152 | AGAAAGCTTCCAGTC[A/G]TGGCAGGAGGTGAAA | 10277 |
rs755995935 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142798 | CCACCCCACCTTACT[A/G]TATTTTCAAAGCCAG | 10277 |
rs755996153 | snp | A/C/G | 4.99399e-05 | 0.00499679 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106444 | TCGAGCTCCCCAAGT[A/C/G]CCCCTGCCCTCGCCA | 10277 |
rs756001442 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045844 | GAGTTGCATGTGGAG[C/T]ATGAAAGAGTGGAGT | 10277 |
rs756013292 | snp | C/T | 1.6525e-05 | 0.00287441 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095421 | ATAACTTGAACATTA[C/T]TTCACATGGGGCTTC | 10277 |
rs756021642 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063910 | TGAAACTGTCTCAAT[-/G]AAAAAAAAAAAAAAG | 10277 |
rs756059766 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112284 | GCTCTTAGGACTTCA[A/G]TATGACATATTTCCA | 10277 |
rs756060004 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124800 | AATCAGTGCTAGGAG[A/G]TATTCATTTGAAAAT | 10277 |
rs756099084 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094681 | CCTTGTGATTCACCC[A/G]CCTCGACCTCCCAAA | 10277 |
rs756106382 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038647 | CCACAGCTTTTGTAT[C/T]AACATCCTACGTAAC | 10277 |
rs756112057 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081142 | ATCTTGGCTCACCGC[A/C]ACCTCTACCTCCTGG | 10277 |
rs756118043 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | UBE4B | GRCh38.p7 | 1:10119477 | GAATTGTATTGTTTG[C/T]TTCTTGTCGTCCTCA | 10277 |
rs756124438 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046513 | AATACTCTGCGCTGG[C/T]CCATAGCCATTGTCA | 10277 |
rs756143102 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159219 | TCATTCTTTGTGGTA[A/G]GGCCCTAAACCTTAA | 10277 |
rs756146634 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154843 | GCAAATCTCCATCTC[-/A]AAAAAAAAAAAAAGG | 10277 |
rs756168925 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10099137 | ATCCCAGTTATTTGG[C/G]AGGCTGAGGCAGGAG | 10277 |
rs756188003 | in-del | -/TTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067731 | CCATCTCAGTATTTG[-/TTG]TTGTTGTTGTTGTTG | 10277 |
rs756207925 | in-del | -/AAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071845 | CAAAATACAGTTGTT[-/AAA]AACTCAAGTGATAGA | 10277 |
rs756224246 | snp | A/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158417 | AATTCGCTATCATAT[A/T]AGCACCATTTTTAAA | 10277 |
rs756270935 | snp | A/C | 1.66225e-05 | 0.00288287 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10134988 | TTTCAACTTTCACAG[A/C]CAGATGATAGATTGG | 10277 |
rs756295010 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084273 | ATCTTATGGCTTAGT[A/G]GGAGAGATAATACAT | 10277 |
rs756307190 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098384 | AAATGAGGAACAGAA[A/G]GGAGTATCTTTAAAC | 10277 |
rs756330307 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116978 | TGGAGAGTTTCTTAA[C/G]CTTTGGTTCTATTGC | 10277 |
rs756361238 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067842 | ACGCCATTCTCCTGC[C/G]TCAGCTTCCCGAGTA | 10277 |
rs756362129 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085665 | TAGGTTTTTTTTTAA[C/T]ATCAGTTCTATCATT | 10277 |
rs756373953 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048217 | TTGGCTTAAGCAGCT[C/T]AAAAAATGGAATTGT | 10277 |
rs756393620 | snp | C/T | 1.65263e-05 | 0.00287452 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10121976 | GGTCCTTGCAGCAGC[C/T]GTCCTTCCTAGTGCC | 10277 |
rs756395634 | snp | C/T | 1.69729e-05 | 0.0029131 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135138 | CCCAATGATGAGACG[C/T]GTGTGAATGCAACGA | 10277 |
rs756405907 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037324 | GAGCCACTGTGCCCG[A/G]TAGTCTTGTGCTTTT | 10277 |
rs756408156 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037315 | TACAGGCATGAGCCA[C/G]TGTGCCCGGTAGTCT | 10277 |
rs756419977 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116237 | AACAACCTCCTCCCA[C/T]GGTCAAGTGATTCTT | 10277 |
rs756446524 | snp | A/G | 3.55999e-05 | 0.00421885 | intron-variant | UBE4B | GRCh38.p7 | 1:10126758 | CTCTTAGATTCTCTT[A/G]AACTTATATTTCTGA | 10277 |
rs756483326 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063476 | CACTTTTTACTTCCA[A/T]ATAACAGCCAAGTTC | 10277 |
rs756527752 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097163 | TAGCTGAAGAAAGAA[C/T]TGACAAACTGAAAGA | 10277 |
rs756534871 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171888 | TCTGTCTCAAAATAA[A/G]TAAATAAGTAAGTAA | 10277 |
rs756549657 | snp | A/G | 1.68672e-05 | 0.00290402 | intron-variant | UBE4B | GRCh38.p7 | 1:10179371 | TTTTCTTTTTCAGTC[A/G]TGGGCTCTCAGTAGA | 10277 |
rs756555260 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140184 | TTACTCAGTTCAAAA[C/T]GTTTTCTAATTTTTG | 10277 |
rs756559591 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178788 | GCACGCGCAGAAATC[A/G]ACTACAGCGACGCTC | 10277 |
rs756579687 | snp | A/G | 1.69804e-05 | 0.00291374 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033664 | TTTCACCATTAAGAG[A/G]AAAGCGATGGAGGAG | 10277 |
rs756582691 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109713 | TGGAGTGCAGTGGAG[C/G]GATCTCGGCTCACTG | 10277 |
rs756594243 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109016 | ACCTCTCTTTCTGGA[C/T]TTCTAACACCCCAGC | 10277 |
rs756601797 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040120 | AGAAAGCACATGTTT[-/C]CTTTTTTTTTTTTTC | 10277 |
rs756609895 | snp | A/C | 0.000124472 | 0.007888 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106545 | CGCCTCACCCAGTGC[A/C]ACGAGCAGACGCCCC | 10277 |
rs756660786 | snp | A/G | 1.64909e-05 | 0.00287144 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101063 | ACAGTGACATTGTGC[A/G]GATTTATAAAAGGTA | 10277 |
rs756665608 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112415 | TTTTGTTTTGTCTTG[C/T]TTTAGACGGAGTCTC | 10277 |
rs756717797 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | UBE4B | GRCh38.p7 | 1:10147124 | GTTTCCCTTGTCCCT[C/T]CTTGGCTGGGCTCTG | 10277 |
rs756736306 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077844 | CTAGTGCCTATGGAA[C/T]CAAGTCCACAGGTCA | 10277 |
rs756752915 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | UBE4B | GRCh38.p7 | 1:10130702 | TGACTGCATTTTTTC[C/T]TTCTCTTTCCAGGTT | 10277 |
rs756773516 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079215 | GGAGTCCCGCTCTGT[C/T]GCCCAGGCTGGAGGG | 10277 |
rs756774255 | snp | A/G | 1.66835e-05 | 0.00288816 | intron-variant | UBE4B | GRCh38.p7 | 1:10179865 | GCCCTCCCATCTGGG[A/G]CATTAATCCTCCTTT | 10277 |
rs756822586 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156838 | GCTGTTTCCTTTTTT[-/G]GTCACACACAAAAAA | 10277 |
rs756832690 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109823 | ACCTGGCTAATTTTT[A/G]TATTTTTAGCAGAGA | 10277 |
rs756845127 | snp | C/T | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117521 | ATTTCACCATTGAAA[C/T]CTGCAAAGAGACAGA | 10277 |
rs756856155 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056353 | GATGGAGAAAACTGC[C/T]AGGCTGAAATTATTT | 10277 |
rs756858013 | snp | A/G | 1.6609e-05 | 0.0028817 | intron-variant | UBE4B | GRCh38.p7 | 1:10119462 | ATTTTTAACAGCATG[A/G]AATTGTATTGTTTGT | 10277 |
rs756860057 | in-del | -/GC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082369 | GCCAGGCATGGTAGT[-/GC]GCGCACCTGTAGGCC | 10277 |
rs756884914 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089977 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCTGG | 10277 |
rs756911121 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042941 | CAGGAATAGCAAGGA[C/T]GCCAAGCATGGTTAG | 10277 |
rs756912152 | snp | C/G | 1.65198e-05 | 0.00287395 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179963 | GATCACTAAACCGTT[C/G]CGCCGCCCACCCTCT | 10277 |
rs756938091 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091189 | GTTACAGCAGATTAT[A/G]TTCATTTTTTAATTC | 10277 |
rs756987417 | snp | C/G | 8.60504e-05 | 0.00655879 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171099 | CCTTTTCACTTGTCT[C/G]AACAGCATGAATTGT | 10277 |
rs756997456 | in-del | -/ACTGACTGATCTTTGGGTGGGG | 8.29511e-05 | 0.00643962 | intron-variant | UBE4B | GRCh38.p7 | 1:10146922 | TGTAGGGACTTAGCT[-/ACTGACTGATCTTTGGGTGGGG]ACTGACTGATCTTTG | 10277 |
rs757016765 | snp | A/G | 1.68681e-05 | 0.00290409 | intron-variant | UBE4B | GRCh38.p7 | 1:10103127 | GTCTTACTGCAGAGT[A/G]CTCGACAAGAAAATA | 10277 |
rs757018685 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055266 | TCGTAGGCCACCTTT[C/T]CATCATTTTTTCTTT | 10277 |
rs757021298 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144552 | CAGCCTGCCCAACAT[A/C]GTGAAACCTCATCTC | 10277 |
rs757023430 | snp | A/G | 1.66101e-05 | 0.0028818 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106260 | TCCCGTGATGGGCCC[A/G]TCTCTTGCCTCACCT | 10277 |
rs757031473 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177240 | GAAAAGAGGTTTAGG[C/G]CGAGCACAGTGGCTC | 10277 |
rs757042946 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143673 | GGAGGAGCCATTCTT[C/T]TGTCTACCATACTCA | 10277 |
rs757044747 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158132 | AGTTTTCCTAGCCCC[A/G]TTCCTTTAGGTGTTG | 10277 |
rs757045554 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069620 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 10277 |
rs757074810 | snp | G/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072118 | AGGGAGAACCCTCCG[G/T]GGCCTCCCATAGCGG | 10277 |
rs757101050 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113345 | TCCAGTCACCTCCCA[C/T]TAGGCCCGTGCTCCA | 10277 |
rs757111718 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171305 | GGACTGTGCTCGGTT[C/T]GCGAAAGCCATTGCT | 10277 |
rs757114010 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101798 | AGGCGTGAGCCACTG[C/T]GCCTGGCCTGGTCTT | 10277 |
rs757149949 | snp | A/G | 6.62899e-05 | 0.00575678 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106355 | GAACTGCTGCGGGAA[A/G]CCAGCCTTCATCCCC | 10277 |
rs757174545 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126555 | GGGGGTCCTGTCAGA[A/G]TATTAGAGTTCACCA | 10277 |
rs757222911 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074347 | ATCTCATATGGCCTT[-/T]TTTTTTTTTAACAGC | 10277 |
rs757222939 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041335 | ACCTTTTTGGCATTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs757238394 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040578 | ATGTAGACCCCCACT[C/G]TGGCCTTGGTGCTCT | 10277 |
rs757267546 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181112 | GAAACCATAAAGTGT[C/T]CTGAAGAAATTAAGT | 10277 |
rs757274612 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072183 | CAATGTCCACAACAT[A/G]ACCCCAGCTACCTCC | 10277 |
rs757275818 | in-del | -/CACAAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166968 | ACACACACACACACA[-/CACAAAAA]AAAAAAATTAGCTGG | 10277 |
rs757284036 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068831 | GGCATTCAGACCACC[C/G]AAGGGCATTATCCTC | 10277 |
rs757343142 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119484 | ATTGTTTGTTTCTTG[C/T]CGTCCTCACTTCCAC | 10277 |
rs757353202 | snp | A/G | 3.30579e-05 | 0.00406544 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178779 | GCCAAGAACGCACGC[A/G]CAGAAATCGACTACA | 10277 |
rs757383030 | snp | C/G | 1.75993e-05 | 0.00296637 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106537 | CTACCACCCGCCTCA[C/G]CCAGTGCCACGAGCA | 10277 |
rs757431421 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117803 | ACTCACATTCTAATA[C/G]AGACAGAGCCAAGGT | 10277 |
rs757431752 | snp | A/G | 1.65496e-05 | 0.00287655 | intron-variant | UBE4B | GRCh38.p7 | 1:10095631 | CTAATATGCTCTTTT[A/G]TTTAGGGAAAGAGAA | 10277 |
rs757437020 | snp | A/C/G | 0.000114111 | 0.00755272 | intron-variant | UBE4B | GRCh38.p7 | 1:10168312 | GGTGGTTTGGACTCC[A/C/G]CATTCAGACTCTCTC | 10277 |
rs757472933 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086521 | TATCCTTTTTAGCTA[C/T]AAGAGTTAGGTGGAT | 10277 |
rs757477927 | snp | A/G | 0.000126797 | 0.0079613 | intron-variant | UBE4B | GRCh38.p7 | 1:10178871 | AGTTAACTGGAAATC[A/G]ATAACATTACAAGAG | 10277 |
rs757481697 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093528 | ATGTGAAGAACTGCT[G/T]TCAGGAATGGATAAA | 10277 |
rs757493497 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072507 | GAATTTGGTTCTGCT[G/T]ATTTTATGAATTTGG | 10277 |
rs757502392 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160682 | CCAGGTGTGGTGGCT[C/T]ATCTCTGTAATCCCA | 10277 |
rs757565803 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137104 | TGAGCCGAAATTCCC[C/T]ACGGAGTGCTTCTTT | 10277 |
rs757568104 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105843 | TTAATCAGTGTCATA[C/T]AGGGTATGGCATATA | 10277 |
rs757593863 | snp | A/G | 1.66205e-05 | 0.00288271 | intron-variant | UBE4B | GRCh38.p7 | 1:10161315 | CCAGAGGCTTGGACA[A/G]CTTTGCAGGCCATCT | 10277 |
rs757625036 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137174 | TGCCGTCGCTATATC[C/T]GCAGACTCCGGGCTA | 10277 |
rs757634265 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180487 | TATTCTGTGAGATAA[C/G]TGTGCCTGCTACCAA | 10277 |
rs757678873 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172641 | TAGGCATTCTAGAAG[A/G]TTCTTTACCCATATC | 10277 |
rs757697011 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174050 | CTGTTCTTCCAGAGT[A/G]GTGAAACAAACACAC | 10277 |
rs757698451 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140612 | GATACAGTCACTCCC[A/G]CTGGCTTTAGAGGGT | 10277 |
rs757698933 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159542 | GCCAGGCATGGTGGT[A/G]GGCGCGGTGGCGGGC | 10277 |
rs757725666 | snp | A/C | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105563 | ATTTTAATGGAAGTG[A/C]TAATGATGTCCACTC | 10277 |
rs757734667 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097506 | GGCCAGGAGCATTTG[A/G]AAGATATTATTTTAA | 10277 |
rs757748660 | snp | C/G | 1.6703e-05 | 0.00288985 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106466 | CCCTCGCCAGTAGCC[C/G]CCAAGCAGTGCCCGC | 10277 |
rs757749684 | snp | C/G | 1.64931e-05 | 0.00287163 | intron-variant | UBE4B | GRCh38.p7 | 1:10137246 | GGATTGCCTGAGTTA[C/G]CACTTTTTCTCAGGG | 10277 |
rs757751628 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10129415 | TGAGCTCTGTGAAAC[C/T]AAGTTTGGGAAGACA | 10277 |
rs757761655 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160104 | CTTTTTTTCTCTACG[A/G]ATCTGGCATCTCCAG | 10277 |
rs757779685 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063663 | TAATTCCAACACTTT[G/T]GGAGGCCAAGTCAGG | 10277 |
rs757805094 | snp | C/T | 4.94588e-05 | 0.00497262 | intron-variant | UBE4B | GRCh38.p7 | 1:10130456 | ACATTTTTACCCCAC[C/T]GGCCTGTTCAGCGGC | 10277 |
rs757857357 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065269 | GAAGGGAAGGCTTCA[C/T]TGAGAAGGTAACATT | 10277 |
rs757876043 | snp | A/G | 1.65999e-05 | 0.00288091 | intron-variant | UBE4B | GRCh38.p7 | 1:10145083 | GACCAGCCTCATAGT[A/G]ATAATTTTCCCAACA | 10277 |
rs757878788 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049367 | GGGGGTACGGTTGAT[C/G]GGGCAGTTAATTCTG | 10277 |
rs757892054 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153336 | CATGGCGAGACCCCA[C/T]CTCTACGAAAAATTT | 10277 |
rs757933390 | snp | C/T | 4.94344e-05 | 0.00497139 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072116 | AGAGGGAGAACCCTC[C/T]GGGGCCTCCCATAGC | 10277 |
rs757945257 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141638 | GCTTCTGTTGCATCC[A/G]ATTTTGTAATAATGC | 10277 |
rs757945478 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154404 | AAAAAGAGTGGATTT[-/G]GAGCTACGAGACAAC | 10277 |
rs757968019 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082993 | GGACATGATCTCATT[C/G]TTTTTTACGGCTGCA | 10277 |
rs757983184 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130565 | GCGGGAGCTGCAGAG[A/G]CTCTCTTACTTAGGG | 10277 |
rs758011399 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093197 | ATTTACTACCATAAT[A/G]ATCATTGAAGTTTAT | 10277 |
rs758013386 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077992 | GAATGCCACTTTTTT[A/G]TAGTTAACACTGATT | 10277 |
rs758014435 | snp | C/T | 4.95618e-05 | 0.00497779 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179536 | CCTTCAACCGGCAGA[C/T]GCTGACAGAGAGCAT | 10277 |
rs758052706 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098848 | AAATCAGCAATAAGA[A/C]CAAGGATGACTGCTA | 10277 |
rs758086346 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123335 | ACTTGGGAGGCTGAG[A/G]TAGGAGAATTGCTTG | 10277 |
rs758107884 | snp | C/T | 6.58892e-05 | 0.00573936 | intron-variant | UBE4B | GRCh38.p7 | 1:10130668 | TATTCAGATTCTTTC[C/T]CAAATGTGCATTATA | 10277 |
rs758137214 | snp | A/G | 1.67203e-05 | 0.00289134 | intron-variant | UBE4B | GRCh38.p7 | 1:10121946 | ATCACCGTCCCTAAT[A/G]TTCATGGGTCCACAG | 10277 |
rs758182185 | snp | C/T | 1.65231e-05 | 0.00287424 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168198 | GTCCCGCTCTTACCT[C/T]GCCCTGGCCACCGAA | 10277 |
rs758189689 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155707 | CTCTTAACACCACAG[A/G]GATAGTATTCTAGCT | 10277 |
rs758215455 | in-del | -/A | 0.000303915 | 0.0123234 | frameshift-variant, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117584 | GAGTTGGAATAGAGG[-/A]AAAAAAAGCACCAAA | 10277 |
rs758222266 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057916 | GCAAGCATGGGAGGC[A/C]GTGGAGGGTATGTAG | 10277 |
rs758223047 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101978 | GCTCTGCATTTAGGG[G/T]GTGTGTGTGTGTGTG | 10277 |
rs758237181 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170672 | ATTTGTATCTGATAA[C/G]TACATAAGAATGACA | 10277 |
rs758244356 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091395 | ATATTTAATTCACAT[C/T]GATTTCTAAATAAAA | 10277 |
rs758247755 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132982 | TCGGGTTAGGTTTAC[A/G]TGATCAGAACTGTCA | 10277 |
rs758253528 | in-del | -/TTTCTTTCATTTGACTGTTAGTC | 2.4211e-05 | 0.00347921 | intron-variant | UBE4B | GRCh38.p7 | 1:10144906 | GATGGATCCGGCTGT[-/TTTCTTTCATTTGACTGTTAGTC]TTTGATTTCAGAACT | 10277 |
rs758275401 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044012 | ATGTTTGTTGTTGGG[A/G]GAGTGACCACAATTC | 10277 |
rs758279310 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098766 | TCTAACTAATATAAA[-/G]GGCATCTACCAAAAA | 10277 |
rs758304065 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180220 | TGTAATAAAGCATGT[C/G]CTTCGTATGTCACAG | 10277 |
rs758356191 | snp | G/T | 1.79014e-05 | 0.00299172 | intron-variant | UBE4B | GRCh38.p7 | 1:10126752 | TTCCCACTCTTAGAT[G/T]CTCTTAAACTTATAT | 10277 |
rs758356465 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103251 | CAATTGTTTAGCCAC[A/T]TTCTTCCCTTTCCAC | 10277 |
rs758368159 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | UBE4B | GRCh38.p7 | 1:10126887 | CTCATGGTAAAACTT[C/T]GTTCTTTTTCTTTAA | 10277 |
rs758376675 | snp | A/G | 1.66432e-05 | 0.00288467 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106252 | AGCTCTGTTCCCGTG[A/G]TGGGCCCGTCTCTTG | 10277 |
rs758381896 | snp | C/T | 5.11461e-05 | 0.00505672 | intron-variant | UBE4B | GRCh38.p7 | 1:10033728 | ACCTTGAGGGATTAG[C/T]TGGCAACTCGTTAGC | 10277 |
rs758405754 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070780 | TTAAAAGGAAGAAGT[A/G]GCAGATTGTATTTTT | 10277 |
rs758413360 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033749 | ACTCGTTAGCGCTTT[C/G]GACAGGGATGGTATT | 10277 |
rs758417894 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168817 | GAATGGCGTGAACCC[-/G]GGAGGCAGAGCTGGC | 10277 |
rs758423694 | snp | A/G/T | 8.29244e-05 | 0.00643868 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106373 | AGCCTTCATCCCCGC[A/G/T]GTATCGCCCCTACAC | 10277 |
rs758424956 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046609 | TTTCTGGCAACCTTG[A/G]TTCTGGTCTCTTGAA | 10277 |
rs758453616 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056444 | TTACCGAGTGCTCTC[G/T]GGGAGTTAGGTACTG | 10277 |
rs758456469 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124964 | AACCCCATCTCTACT[C/T]AAAATACAAAAAATT | 10277 |
rs758468672 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095554 | CTCAGTCTCTCTCAC[A/G]TTCCCAGAGCATGGA | 10277 |
rs758473871 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170390 | TCCAGTTATTACATT[G/T]CATGAAAACCTTGTG | 10277 |
rs758486678 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119164 | GAGATTACAGGCGTG[A/G]GCCACCGTGCCCGGC | 10277 |
rs758558388 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108340 | CCTCCTGGACCTCAG[G/T]GAAGCCAGACCCCAT | 10277 |
rs758559091 | snp | C/T | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178711 | CAGGGATCAAATCCA[C/T]AATAGCAATAGAAAA | 10277 |
rs758590876 | in-del | -/AAAAAAAGAAAAAAAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114089 | AAAAGAAAAAAAAAA[-/AAAAAAAGAAAAAAAAAA]AAAAAGATGCGTTTC | 10277 |
rs758599921 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138526 | GGTGTGAGCCACCGT[G/T]CCTGGCCTAAAATCA | 10277 |
rs758600592 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107018 | CTTAGAAGGAAGCAG[C/T]ATCAGAATTCCACTA | 10277 |
rs758610245 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081340 | GCTGGGATTACAGGT[G/T]TGAGCCACCATGCCT | 10277 |
rs758612905 | snp | C/T | 1.66341e-05 | 0.00288388 | intron-variant | UBE4B | GRCh38.p7 | 1:10149172 | AAATTGTCCTTTTTT[C/T]CTCTTTGACAGTATA | 10277 |
rs758631499 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072755 | TCCAGGACTGTCTTT[G/T]TTGGGAAATGATATT | 10277 |
rs758632886 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148829 | CCTGTAATCTCAGCT[A/G]TTCGGGAGGCTGAGA | 10277 |
rs758641566 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074770 | ACTTCTAAATGTTAG[C/G]ATTCAAGGGCTCAAT | 10277 |
rs758645417 | snp | C/T | 0.00011672 | 0.00763849 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106455 | AAGTCCCCCTGCCCT[C/T]GCCAGTAGCCCCCAA | 10277 |
rs758653687 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094730 | TGAGCCACCACACCC[A/G]GCCTCATTAACATTT | 10277 |
rs758666978 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061035 | ACAGGTGTAAGCCAC[C/T]GCAAGAGTTTGTTTC | 10277 |
rs758681535 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090676 | CCTCTTGCCTCGACC[C/G]CCCAATCTGTTGGAA | 10277 |
rs758701751 | snp | A/G | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158474 | TGGCACCTTTATGGA[A/G]GAGTTCAAGTGAGTA | 10277 |
rs758729231 | snp | C/T | 1.66938e-05 | 0.00288905 | intron-variant | UBE4B | GRCh38.p7 | 1:10179857 | CAGGAAGAGCCCTCC[C/T]ATCTGGGGCATTAAT | 10277 |
rs758746497 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117064 | TATTTTGTCAGTCCC[G/T]TATAACTTTTCCCCC | 10277 |
rs758747155 | snp | C/T | 1.65045e-05 | 0.00287263 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095438 | TCACATGGGGCTTCA[C/T]CCTTCCTGTGTTTTC | 10277 |
rs758787134 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141456 | CTTGTTCTCCCCTAG[-/A]GCCTCCAGAAGGAAC | 10277 |
rs758798535 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162100 | GCTTCTCCGGTTGAA[A/G]CGATTTTCGTGCCTC | 10277 |
rs758800216 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040298 | AATTTTTAGTAGAGA[C/T]GGTGTTTCACCATAT | 10277 |
rs758817230 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103000 | CCTTACAGCTGGTCT[G/T]TAAGATCTTCCGTGT | 10277 |
rs758820734 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066905 | GCAAGACTCCGTCTC[-/A]AAAAAAAAACCAAAA | 10277 |
rs758826237 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161145 | TTGCCTTTCCAGCTC[C/T]GGGAAGCAGTTTGTT | 10277 |
rs758836378 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130053 | AGTTCATTTGAACTT[C/T]ATCCAATAGTATCCT | 10277 |
rs758856764 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086716 | TCTCTTTTTTTTTTG[A/C]GATGTAGTCTCACTG | 10277 |
rs758859803 | snp | A/T | 1.99424e-05 | 0.00315766 | intron-variant | UBE4B | GRCh38.p7 | 1:10117632 | TAACTTAAAAAAAAA[A/T]AAGCCTAGTTATTTG | 10277 |
rs758908464 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083303 | AGGAAAACAGATGCA[A/G]AGGTCCTGGGGCAAG | 10277 |
rs758917857 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139886 | GGCATGTGCCACCAC[A/G]CCCAGCTAATTTTGT | 10277 |
rs758948331 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100050 | GCTGGAGTGCAGTGG[C/T]GCAGTCTTGGCTCAC | 10277 |
rs758993135 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181014 | CACGCGCACACAAGT[A/G]TAAGACTTTTTGTAT | 10277 |
rs759050978 | in-del | -/ACACAAAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166967 | CACACACACACACAC[-/ACACAAAAAA]AAAAAATTAGCTGGG | 10277 |
rs759085308 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034286 | CTAATGACTTCTGGC[A/G]TTCTTCTGTTACATT | 10277 |
rs759105104 | snp | A/T | 2.86833e-05 | 0.00378693 | intron-variant | UBE4B | GRCh38.p7 | 1:10135223 | CGGTCATTAAAACAC[A/T]GCCCTCTTGTCTGTG | 10277 |
rs759133957 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096276 | GTACGGATCAAGGTG[C/T]CTTGAAAGAGCCCTC | 10277 |
rs759141073 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124523 | CCCAGAATTCTGCTG[A/T]CTTTTCAGCCACTCA | 10277 |
rs759143079 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138008 | GGTACGATCTCAGCT[C/T]GGTGCAACCTCTGCC | 10277 |
rs759194537 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126067 | GCACTTTGGGAGGCT[A/G]AGGCGGGTGGATCAC | 10277 |
rs759215980 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161796 | GCACGTGCCGTGCCA[G/T]TACCAGTGCTCTTTC | 10277 |
rs759224634 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035265 | GCCTCCCAAAGTGCT[C/G]GGATTACAGGCGTGA | 10277 |
rs759248268 | snp | C/T | 1.65699e-05 | 0.00287831 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106321 | TCCACTCCCCTCAGT[C/T]CTCACAGTGCAGCCT | 10277 |
rs759258636 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081858 | CCTCCCAAAGTGCTG[A/G]GATTGCCACCATGCC | 10277 |
rs759340929 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131337 | CAAAAATTAGCCAGG[C/G]ATGGCAGCGCGTGCC | 10277 |
rs759377937 | snp | A/C | 8.29236e-05 | 0.00643855 | intron-variant | UBE4B | GRCh38.p7 | 1:10158318 | TTTGGAAAGCAAGAA[A/C]ATACATATCCCTCAG | 10277 |
rs759379212 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151444 | GCCAAACTGGTAGAA[A/G]TCATGTTTATGACCA | 10277 |
rs759407524 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046439 | CCCCCATACAGTGGT[A/G]GAGAGGTTAGGATAA | 10277 |
rs759410145 | snp | A/G | 1.86974e-05 | 0.0030575 | intron-variant | UBE4B | GRCh38.p7 | 1:10106597 | AGGTATTTATCCCAC[A/G]GGAGAGTTGCATGTG | 10277 |
rs759418187 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149608 | ACATCCCAAAACCAG[A/C]AATATCCACATCTAT | 10277 |
rs759435590 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145078 | TTATAGACCAGCCTC[A/G]TAGTGATAATTTTCC | 10277 |
rs759438533 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10033051 | GTAGGAGGATTTACT[A/C]TTCCAGCGAGAGCTA | 10277 |
rs759441274 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074033 | AGCTTAAAACTCCCA[A/G]GCTCAGATGATCCGT | 10277 |
rs759462656 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107816 | CTCCTGACCTCAAGT[C/G]ATCTGCCCGTCTTGG | 10277 |
rs759470061 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087024 | TGGACAAGACCAGAG[A/C]AGATGTTGTGGTAAC | 10277 |
rs759481953 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049077 | TTTGAGACATAATAT[A/G]GGGAACATTGGATCA | 10277 |
rs759485063 | snp | A/G | 0.000197925 | 0.00994602 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101179 | ATCGAAGAGAAAAGC[A/G]GAGCCTCAGTGATAA | 10277 |
rs759502205 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084445 | GCTGTCCCAGTCAAC[A/G]TATTCACCCCAAAAG | 10277 |
rs759518087 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072357 | AGTAGTTTAAATATC[A/G]TTGCAATGTGTTGTG | 10277 |
rs759576338 | snp | A/T | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179928 | AGATTCAGGCGTGGA[A/T]GAGAGAGAAACAGAA | 10277 |
rs759578486 | in-del | -/AAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136930 | CATCTCAAATAAATA[-/AAT]AAATAAATAAACAAA | 10277 |
rs759610657 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151775 | CTACTGGTCTCTGAT[G/T]ATTCAGCAGGAACTA | 10277 |
rs759611637 | snp | A/C | 1.65847e-05 | 0.0028796 | intron-variant | UBE4B | GRCh38.p7 | 1:10102929 | TTGAAATTAACCTGC[A/C]AATCTTCTTCTTCAC | 10277 |
rs759617025 | in-del | -/TTTT | 7.00243e-05 | 0.00591669 | intron-variant | UBE4B | GRCh38.p7 | 1:10178851 | TTTCATGCTGATTTC[-/TTTT]GAGTTAACTGGAAAT | 10277 |
rs759622736 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064485 | TATTTTAAGGATACA[A/G]GAGTCTTCTTTCTGA | 10277 |
rs759623210 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | UBE4B | GRCh38.p7 | 1:10105510 | TTTGTTCTGCCTTTC[C/T]AACAGTATTCTCCGA | 10277 |
rs759626831 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051231 | AAGTACTTAATCTTT[A/C]TGAGCCTCAGTTTCC | 10277 |
rs759647809 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175554 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 10277 |
rs759655728 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121909 | CATGACATTTCACGT[G/T]CCTCTGTAGTGAGTT | 10277 |
rs759661609 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137159 | TCTATTCTGCCTAGT[G/T]GCCGTCGCTATATCC | 10277 |
rs759663394 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050473 | AAGGAGTAGGTGATA[C/G]GGAGAAGTTGGAGGA | 10277 |
rs759665597 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172297 | AACGTCCTCACAGCT[A/C]ATGTTTATTAACTGT | 10277 |
rs759691132 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110612 | ATCCGGAGGAAAATG[-/T]TTTCTAATTGTTTCC | 10277 |
rs759691967 | in-del | -/T | 1.80041e-05 | 0.00300029 | intron-variant | UBE4B | GRCh38.p7 | 1:10134971 | TAAAAATACTTTTTC[-/T]TTTTCAACTTTCACA | 10277 |
rs759695845 | snp | C/G | 1.67066e-05 | 0.00289016 | intron-variant | UBE4B | GRCh38.p7 | 1:10103104 | GAAGGTAGGAATCTA[C/G]CTCAGCAGTCTTACT | 10277 |
rs759696481 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054598 | GCTGGCCTTTAGAGC[A/G]CTTAATGTGCTCAAT | 10277 |
rs759713297 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166464 | CGATAGGCCTCAATA[C/T]GGTGGCACACTGCAT | 10277 |
rs759731139 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141203 | TCTCGGAACCTGTGA[A/C]TATGTTATCTAACTT | 10277 |
rs759738100 | snp | A/G | 3.34213e-05 | 0.00408773 | intron-variant | UBE4B | GRCh38.p7 | 1:10168114 | ACCGAGCCTTACTCA[A/G]CGTCTGTTCGATGTG | 10277 |
rs759777909 | snp | C/T | 1.86879e-05 | 0.00305673 | intron-variant | UBE4B | GRCh38.p7 | 1:10178598 | CAGCTCGCTTTTTTC[C/T]ACCTGACGTACATTT | 10277 |
rs759786941 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110164 | CATCAGGGGTTGGAT[C/T]GCTCTCTCCATCTGC | 10277 |
rs759806963 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043586 | CGCCCACCACCAAGC[-/CT]GACTAATTTTTTTTG | 10277 |
rs759816306 | in-del | -/TTTTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055283 | TCATTTTTTCTTTTC[-/TTTTC]TTTTCTTTTCTTTTC | 10277 |
rs759830214 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165212 | CCACATCTCCTGCCT[A/G]AGTCTGCCCAATCTC | 10277 |
rs759831370 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043717 | ACAGGCGTGATCCAA[C/T]GCGCTGGGCCGGGAT | 10277 |
rs759837059 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077471 | TGTTTTTGATCTGCA[G/T]CTCCTCTTCCCTTTG | 10277 |
rs759852470 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057173 | ATGGGTGACTTAAGA[A/G]AACACTTTAATTAGG | 10277 |
rs759875947 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | UBE4B | GRCh38.p7 | 1:10129357 | CAGTCAGTTTAAGAT[A/G]AAATGCATTTAAATG | 10277 |
rs759880565 | in-del | -/GA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155066 | ACTGTGGCTTCAGGA[-/GA]GAGAGAGAGAGAGAG | 10277 |
rs759881579 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167706 | CAAGCAGTTCTCCTG[A/C]CTCAGCCTCCCAAGT | 10277 |
rs759888990 | snp | A/G | 1.65362e-05 | 0.00287538 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178713 | GGGATCAAATCCACA[A/G]TAGCAATAGAAAAAT | 10277 |
rs759924793 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090859 | AGGCCTAATGTTACA[A/G]GTTAAAGGTAGATAT | 10277 |
rs759929574 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101401 | GATCTGATAATATCC[A/G]TCTGTTTTTGGTTCA | 10277 |
rs759935288 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147005 | GATGCTGGCCTACTT[C/G]ACGAGAGCTTCCTGA | 10277 |
rs759939181 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067652 | GACCCGGCTCTCACC[A/G]GGTTGCACAGACTGG | 10277 |
rs759949915 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169804 | TGGATCACCTGAGGT[C/T]AGGAGTTCCAGACCA | 10277 |
rs759992208 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | UBE4B | GRCh38.p7 | 1:10130657 | TGCTGCCCTTTTATT[C/T]AGATTCTTTCCCAAA | 10277 |
rs759992432 | snp | C/T | 4.94328e-05 | 0.00497131 | intron-variant | UBE4B | GRCh38.p7 | 1:10147100 | TCCCGAGTGAGTGTG[C/T]TTCTTCCTGTTTCCC | 10277 |
rs760001496 | snp | A/T | 1.66117e-05 | 0.00288194 | intron-variant | UBE4B | GRCh38.p7 | 1:10179601 | TGCAGCGCTGGCGTC[A/T]GTACCAAGAGATAAA | 10277 |
rs760026709 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126754 | CCCACTCTTAGATTC[-/T]CTTAAACTTATATTT | 10277 |
rs760036929 | snp | A/G | 1.6823e-05 | 0.00290021 | intron-variant | UBE4B | GRCh38.p7 | 1:10072259 | TTTGTAATTCTTCTT[A/G]GCTTTTTGTTAAGCT | 10277 |
rs760064576 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070040 | AGCACTTTGGGGGGC[C/T]GAGGTGGAAGGATTG | 10277 |
rs760080532 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144192 | GGAGCAAAGCCAGAG[A/G]TAACCTCAGAGAAGA | 10277 |
rs760085664 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176612 | GTGGTATTTCATTGC[A/G]GTTTTGATTTGTATT | 10277 |
rs760106439 | snp | A/G | 0.000104243 | 0.00721876 | intron-variant | UBE4B | GRCh38.p7 | 1:10132508 | TACAGACTGCTTTTC[A/G]CTGTTTGTCAAATTC | 10277 |
rs760112995 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130770 | CCCTGGAAAACACTC[A/G]TGTGGTTAGCCAATC | 10277 |
rs760124731 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090456 | GCTCTGTTTCTAACA[-/G]GGCGAGGAGGTCCTA | 10277 |
rs760134669 | snp | C/T | 4.94417e-05 | 0.00497176 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151388 | TGTTCCTTGTTGTGA[C/T]GTTGTGCAACCAGAA | 10277 |
rs760135045 | snp | A/T | 8.88013e-05 | 0.00666279 | intron-variant | UBE4B | GRCh38.p7 | 1:10117615 | GGTAATATGAAATGG[A/T]TTAACTTAAAAAAAA | 10277 |
rs760141546 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089036 | TTTTGAGATAAAGTC[C/T]CGCTCTATGGCCCAG | 10277 |
rs760152395 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094822 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCTAGGC | 10277 |
rs760162570 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102891 | ACGTATTCCTATTGA[A/G]ACACCTAACTCATAC | 10277 |
rs760182209 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055990 | ATCTACGTTAATCTT[A/G]TCTGTTGAACCAAGT | 10277 |
rs760187638 | snp | A/T | 1.68633e-05 | 0.00290368 | intron-variant | UBE4B | GRCh38.p7 | 1:10151571 | ATACAGGTAGGTTGC[A/T]GGAACACAGTGTAGC | 10277 |
rs760189816 | snp | C/T | 2.35446e-05 | 0.003431 | intron-variant | UBE4B | GRCh38.p7 | 1:10134945 | ATCTCAAAAAAAATT[C/T]TTTTTAATGTTTAAA | 10277 |
rs760271388 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115029 | GCTTCTCAGCCTCAT[C/T]GTCTCCCTTTGCTTT | 10277 |
rs760291597 | snp | C/T | 1.6752e-05 | 0.00289408 | intron-variant | UBE4B | GRCh38.p7 | 1:10122086 | AAGCAGGTACGGTCG[C/T]ATGAGTTTGCTCTTG | 10277 |
rs760307250 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145845 | AGATGGGAATATTCT[G/T]GCTGGTGAGACATAG | 10277 |
rs760321868 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175628 | TGCACTCCAGCCTGG[A/G]CGACAGAGCGAGACT | 10277 |
rs760322635 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115883 | AGTATTTGTGTATCT[A/G]AACATGTCTAAACAT | 10277 |
rs760331328 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157994 | CCTAACTTTTTATCC[A/G]CTGAAGTATGTCCAT | 10277 |
rs760336786 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10035654 | CTTGTGATCTGCCCG[C/T]CTCGGCCTCCCAAAG | 10277 |
rs760401154 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083548 | TCCTATCATTGATTG[C/T]TATATTAAAATCCTT | 10277 |
rs760412397 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063097 | ACATGGTGAAACCCC[A/G]TCTCTAATAAAAATA | 10277 |
rs760425310 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105701 | CCAGGAACAAGCCCC[A/G]TGTTCTGCAGCGTGG | 10277 |
rs760454606 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084636 | CATTGATTTGGGACT[A/G]CACTGGGAGTTTTCT | 10277 |
rs760464256 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147227 | AAGGCGCAGTGGTTC[A/G]CGCCTGTAATCCCAG | 10277 |
rs760471350 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111480 | CCACTGACCTCATTG[-/T]CTCAAACATTATATA | 10277 |
rs760491139 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096497 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 10277 |
rs760499450 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115162 | AATACTTTAATACCA[C/T]ACTTTTTTTTTTTTT | 10277 |
rs760505815 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120441 | GGCCAGAGAATCGTT[C/T]GAACCCAGGAGGTGG | 10277 |
rs760531266 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037872 | AGTAGGTGTTTTAAA[C/G]TGTTTTTCGACAATG | 10277 |
rs760533819 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048728 | CCTTGGTTACCTTGA[C/T]AAGACTGATTTCATT | 10277 |
rs760539841 | snp | G/T | 1.64953e-05 | 0.00287182 | intron-variant | UBE4B | GRCh38.p7 | 1:10129492 | TTTTCAGTGAATATA[G/T]CATAACCCAGAAGGC | 10277 |
rs760565048 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109258 | TAGAAATGCATTCAG[A/C]CTTGAGCATCCTGAA | 10277 |
rs760589057 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112125 | ATGCACGTGTAATCC[C/G]TAGGCACATTTACAT | 10277 |
rs760591614 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095576 | GAGCATGGATATCGA[C/T]GGTGTCTCATGTGAG | 10277 |
rs760592143 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075703 | ACAGATTTTCATGAT[C/T]TCCTAAATAAGTGAA | 10277 |
rs760592510 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060511 | GCCCATGACTGTATT[A/T]CCTCTCTGACTTCCC | 10277 |
rs760596347 | snp | C/T | 6.86471e-05 | 0.00585823 | intron-variant | UBE4B | GRCh38.p7 | 1:10149317 | TACATAGTTCTAATA[C/T]GTTTTTATGCATAAT | 10277 |
rs760641074 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058213 | ATTCTTTGGAGAAGA[A/C]ATGTGGTTAATCAAT | 10277 |
rs760645445 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062098 | TATTTTTAGTAGAGA[C/T]GGTGTTTCACCATGT | 10277 |
rs760650066 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176761 | TTTTGTTGTTGAGTT[A/G]GAAGAGTTCTTTTTT | 10277 |
rs760664556 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078014 | CACTGATTATGCTAG[-/T]TTTTTTTTTTTTTGA | 10277 |
rs760677775 | snp | C/T | 3.32127e-05 | 0.00407495 | intron-variant | UBE4B | GRCh38.p7 | 1:10179597 | GAGGTGCAGCGCTGG[C/T]GTCAGTACCAAGAGA | 10277 |
rs760728545 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095321 | TTTCCAGCTTTTTAT[A/G]TAATCTTCTGATAGA | 10277 |
rs760748985 | snp | A/T | 1.85686e-05 | 0.00304695 | intron-variant | UBE4B | GRCh38.p7 | 1:10106586 | GGATCTCTCCTAGGT[A/T]TTTATCCCACAGGAG | 10277 |
rs760766057 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117408 | AAATGCAAACTCTGC[C/G]AAAAATAATCAAGAG | 10277 |
rs760772718 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141303 | GTGGGTAGGTCCAGT[A/G]TCATTGCAAAGGTCT | 10277 |
rs760782510 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128510 | TAAAGGTGTTTCTGC[-/CT]GGCTCCCCACCCCAG | 10277 |
rs760784953 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111395 | CTTGTTTCTCCCCTT[C/T]GGACCACTCTCCCCA | 10277 |
rs760795427 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080137 | CTGATTGAAAATTCT[A/G]CTGGCTGGGTGTGGT | 10277 |
rs760809804 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101167 | TTGATGAAAATGATC[A/G]AAGAGAAAAGCGGAG | 10277 |
rs760819326 | snp | C/G | 6.667e-05 | 0.00577326 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117575 | GTTTCGACCGAGTTG[C/G]AATAGAGGAAAAAAA | 10277 |
rs760820874 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039747 | ACGTGGCTGAGTTTG[A/G]ACTTTCTCTGTAAAA | 10277 |
rs760832653 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173888 | AAGGAATGCTTTGAG[C/T]GGCCTTTGTTTGGTG | 10277 |
rs760854448 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050944 | TTAAGGTAGGCACTT[C/G]ATGAAAAAAGCCTCA | 10277 |
rs760902301 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166943 | AAAATAAATAAATCA[-/CA]CACACACACACACAC | 10277 |
rs760919661 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099583 | AAAAAATTTTGGTCA[A/G]AATCCCGGGAGGGTT | 10277 |
rs760926304 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090155 | GGCATGGTTTCACTT[-/TG]TTGCCCAGGCCGAAG | 10277 |
rs760943458 | snp | A/G | 1.65707e-05 | 0.00287838 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179913 | CAGAACTGAAAGAGC[A/G]GATTCAGGCGTGGAT | 10277 |
rs760964695 | snp | A/G | 3.30038e-05 | 0.00406212 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145020 | GCGAAATGCTGAAGC[A/G]CTGTAAAACTCAGCT | 10277 |
rs760967565 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064688 | TCTGTGCCTACTGTG[C/T]ACTGCTGTACATGGC | 10277 |
rs760996975 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044743 | CACGCCATCATGCCC[A/G]GCTAATTTTTTGTAT | 10277 |
rs761010288 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123024 | TGTTGTGTATTCTGT[C/G]TGGAATTCACTAGCT | 10277 |
rs761013165 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173046 | TGTAAGTAAATTCTA[-/T]GATGTTTACACAGCA | 10277 |
rs761015056 | in-del | -/TC | 1.6528e-05 | 0.00287467 | intron-variant | UBE4B | GRCh38.p7 | 1:10130829 | TAAGTGTTCAGAAAA[-/TC]CAAATCCAGAGGAAG | 10277 |
rs761019133 | snp | G/T | 1.65263e-05 | 0.00287452 | intron-variant | UBE4B | GRCh38.p7 | 1:10137019 | AGCTTTTTCTCTGAT[G/T]GAGACATGTAATAGA | 10277 |
rs761055464 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091002 | TAGAATGCATAATTT[C/G]CTTTAGCAAACTCTT | 10277 |
rs761063229 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074078 | CATGTAGCTGGGACT[A/G]TAGGCATGTGCCACC | 10277 |
rs761084592 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041728 | TTTAAGACAGAGCCT[C/G]GCTGTGTCCCCATGC | 10277 |
rs761084656 | snp | C/T | 1.78659e-05 | 0.00298875 | intron-variant | UBE4B | GRCh38.p7 | 1:10168284 | CGGTGAGTAGAAACC[C/T]GGGGCTCTGTTTGGT | 10277 |
rs761119919 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165418 | GCCCACTGCTTGGTC[G/T]TCAACCTCCACTCTT | 10277 |
rs761137792 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171186 | TTTAATCTTCAGCAA[C/T]TTTGTGGCCCCAAGT | 10277 |
rs761142115 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103981 | TGGCCAGGATGGTCT[C/T]GATCTCTTGACCTCG | 10277 |
rs761153808 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10170275 | CAACTCTGTCCTGTT[A/G]TGACTCTTTTATTTC | 10277 |
rs761167423 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110470 | TACAGCAAACCTCCT[G/T]TAACAGACCTTCATA | 10277 |
rs761176154 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058894 | GGAGTGGCACTATAA[A/G]GGTCTGACTGGCCTC | 10277 |
rs761189613 | snp | A/G | 3.31433e-05 | 0.0040707 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106293 | CCGTGCAGCCAGCCA[A/G]TTGGCTGTGCCTTCC | 10277 |
rs761196320 | snp | C/T | 0.000123724 | 0.00786427 | intron-variant | UBE4B | GRCh38.p7 | 1:10072548 | TAAGATAAAATAATC[C/T]GAAAATGCAAGATTA | 10277 |
rs761196574 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038656 | TTGTATCAACATCCT[A/G]CGTAACACTGACCCA | 10277 |
rs761207145 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072066 | ACTTGCTGGTGGACA[C/G]ACCTCTCAGCCAACC | 10277 |
rs761214629 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146939 | CTGACTGATCTTTGG[A/G]TGGGGACATCCCTGC | 10277 |
rs761228558 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10146973 | CACAGAAACTGGTAC[A/G]GTGCAAGGCCTGTGC | 10277 |
rs761237405 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166879 | GCAGTGAGCCAAGAT[C/T]GCGCCACTGCACTCC | 10277 |
rs761238658 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117889 | ACCGCCAGTGACTCA[A/T]ATGGCCCTGATAATT | 10277 |
rs761245495 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044994 | TTTTCTGTAAGTAGA[C/T]GGTCCATCTAGGGGT | 10277 |
rs761257139 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122156 | CTGACCATTGAAAAC[A/T]TTTGCCTGAATTCGA | 10277 |
rs761275193 | snp | C/T | 4.95274e-05 | 0.00497607 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178750 | TGCTCGCCGAGAAAG[C/T]GGAGGAGATAGTGGC | 10277 |
rs761330124 | snp | A/G | 3.32469e-05 | 0.00407705 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149278 | TTTTTATTTTTTATT[A/G]TACAGTAAGTGCCTT | 10277 |
rs761335727 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072148 | GCATCAGCCCCAGGA[C/G]CCTCTCAGAGTCTTG | 10277 |
rs761340424 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167260 | GCCTGACCAACATGG[-/A]GAAACCCCGTCTCTA | 10277 |
rs761346515 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142170 | GCTACCAGTGTTCCA[C/T]CCTCAAATACTAATT | 10277 |
rs761347150 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043860 | TCAGTTGAGTGCTAC[A/G]GTGTTAAAATTAGTT | 10277 |
rs761353420 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070262 | CTGGGTGACAAGAGC[A/G]AAACTCCGTCTCAGA | 10277 |
rs761416677 | snp | A/G | 0.000102182 | 0.00714705 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106512 | GAGGCCCAGCAGCAC[A/G]GGTCCACCCCTACCA | 10277 |
rs761417416 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160103 | TCTTTTTTTCTCTAC[A/G]AATCTGGCATCTCCA | 10277 |
rs761423154 | snp | A/T | 2.46339e-05 | 0.00350946 | intron-variant | UBE4B | GRCh38.p7 | 1:10134942 | CCCATCTCAAAAAAA[A/T]TTTTTTTTAATGTTT | 10277 |
rs761454523 | snp | C/T | 1.65512e-05 | 0.00287669 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151351 | CAGGCGCTTTATGAG[C/T]CCTGTACTCAGGATA | 10277 |
rs761459470 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146176 | TGCTTAAATTGCCAG[A/G]CATGGTGGCTCACAC | 10277 |
rs761471741 | snp | A/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095550 | CAATCTCAGTCTCTC[A/T]CACGTTCCCAGAGCA | 10277 |
rs761477304 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088671 | CCACCACGCCTGACC[A/G]TATTTTATTATTTTA | 10277 |
rs761487878 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104580 | AAAAAAAAAGTCCTT[C/T]GTATTTCTGGAGGAT | 10277 |
rs761500496 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116697 | TCTCAGAGGATAGTT[A/G]CTACTAACATAACAG | 10277 |
rs761522866 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132461 | TGTCGTCAATGCCAA[C/T]ATGAAGAAAGCACAG | 10277 |
rs761542371 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070536 | CCACCAAGGATAACC[A/G]TTATCCAAACTAATG | 10277 |
rs761566326 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117367 | TTGTTATGTGTACAG[G/T]GATCCTAACAGGCTT | 10277 |
rs761569186 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050323 | GTGATCCGCCTGCCT[A/T]GGCCTCCCAAAGTGT | 10277 |
rs761577852 | snp | A/G/T | 6.58994e-05 | 0.00573986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119556 | TTCTGAGCAACATCC[A/G/T]CTCACAGTGCATATC | 10277 |
rs761577946 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057828 | GCTTTATTTTTGAGA[C/T]ATTTACTCACCTGGG | 10277 |
rs761593672 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071680 | ACATACAGTATATAC[A/G]TATTTATGTATGTAT | 10277 |
rs761612473 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159092 | TTTGGTGTTTTCTAC[A/G]ATGACAGTGTTAAAT | 10277 |
rs761660838 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056202 | ATCTTTTTGGTTTCT[C/G]TTGCTCCTAATTTCA | 10277 |
rs761666555 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128004 | TAAGTGGATTTATGC[C/T]AGAGCTCTTTCCATT | 10277 |
rs761676563 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097941 | CGTGGCACAATCTCG[A/G]CTCACTGCAACCTCC | 10277 |
rs761713643 | snp | A/C | 4.98517e-05 | 0.00499233 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106416 | ATGGGCGTCCTCAGG[A/C]GTCTCCATTCTGTCG | 10277 |
rs761718607 | snp | C/G | 1.64741e-05 | 0.00286998 | intron-variant | UBE4B | GRCh38.p7 | 1:10178618 | GACGTACATTTACGT[C/G]TCACATTGCCATTCC | 10277 |
rs761721041 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085792 | CTCCTGTATTCAGTG[A/T]CTTTTTTTTTTCTTT | 10277 |
rs761724316 | snp | A/G | 9.88338e-05 | 0.00702902 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137147 | GCTCACCACCTCTCT[A/G]TTCTGCCTAGTTGCC | 10277 |
rs761731573 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129326 | AGTTAAAACTGTTTC[C/T]TTATGCTACAAATGA | 10277 |
rs761776399 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096608 | GCGCCTGTAATCTCA[C/G]CTACTGGGGAGGCTG | 10277 |
rs761777175 | snp | A/G | 1.64972e-05 | 0.00287199 | intron-variant | UBE4B | GRCh38.p7 | 1:10129348 | TACAAATGACAGTCA[A/G]TTTAAGATGAAATGC | 10277 |
rs761794975 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159005 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 10277 |
rs761825845 | snp | G/T | 1.65501e-05 | 0.00287659 | intron-variant | UBE4B | GRCh38.p7 | 1:10146941 | GACTGATCTTTGGGT[G/T]GGGACATCCCTGCTT | 10277 |
rs761835369 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103774 | TTGGGATTACAGGCA[C/T]GCGCCACCACACCCA | 10277 |
rs761843670 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142056 | GTCATTTTTTTTTTT[-/C]TATAAGCTCCACCAC | 10277 |
rs761854862 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141086 | TGCTGATCAAGCATC[C/T]TCAGAATCCATTCCC | 10277 |
rs761857109 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058631 | CACAGTGACCACAGT[-/CA]CAGTGCTGCATCCTG | 10277 |
rs761863185 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083858 | GTTTTATTAGTTCTG[A/G]GCTTTATCTTACAGC | 10277 |
rs761876977 | snp | A/G | 1.87419e-05 | 0.00306114 | intron-variant | UBE4B | GRCh38.p7 | 1:10106603 | TTATCCCACAGGAGA[A/G]TTGCATGTGTGTTTG | 10277 |
rs761889732 | snp | C/T | 4.94613e-05 | 0.00497275 | intron-variant | UBE4B | GRCh38.p7 | 1:10129475 | CCTGATGGGCTTGCA[C/T]ATTTTCAGTGAATAT | 10277 |
rs761906824 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130505 | TTCTGCCTAGGTTGC[C/T]TCTTTGCGGTTGTGG | 10277 |
rs761946349 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074931 | GATTGACACATCCAG[C/T]GCTTTACCTGACATC | 10277 |
rs761955109 | snp | C/T | 1.66043e-05 | 0.00288129 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072034 | ATGTTGTAGATTCGA[C/T]GGAGGCGCCTTGCAC | 10277 |
rs761980171 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143285 | CAGGTGTCTATAATT[A/C]CAGCTACTTGGGAGG | 10277 |
rs762002218 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163248 | TTAAAAAAATTTTTT[A/T]TATAGAGACAAAGTC | 10277 |
rs762031334 | snp | A/G | | | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107305 | AAGAAGAAGATGATG[A/G]TGATGGTGATGGTGA | 10277 |
rs762039750 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036316 | AGAAATAGAATAAAC[-/TT]TTTTCAAGGTCAACA | 10277 |
rs762082235 | snp | C/T | 0.0002252 | 0.0106089 | intron-variant | UBE4B | GRCh38.p7 | 1:10107379 | TTTGGGTCCAGGTAT[C/T]AGAGGAATGGAGTCT | 10277 |
rs762089422 | snp | A/G | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168152 | ATCAGCAGCAGGCTC[A/G]TCAGTCTCAGCTTGC | 10277 |
rs762095924 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067551 | CTATTTTTTGGTGTG[C/T]ATCTCATATGTTCTG | 10277 |
rs762098095 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178899 | GAGGACGTCCTGTGC[A/C]ATTAATTTTTTAATG | 10277 |
rs762104627 | snp | C/T | 1.65987e-05 | 0.00288082 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179468 | GCTGCCCTCTGGCAC[C/T]ATCATGGACCGCTCC | 10277 |
rs762125838 | in-del | -/AAAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039078 | AACAAACAAACAAAA[-/AAAC]ACACACACAGAAAAA | 10277 |
rs762130708 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155788 | AGCACTTTGGGAGTC[C/T]GAGACAGGTGAATCA | 10277 |
rs762171599 | in-del | -/T | 3.40872e-05 | 0.00412825 | intron-variant | UBE4B | GRCh38.p7 | 1:10126779 | ATATTTCTGATTTTG[-/T]TTTTTTTCTTATAGA | 10277 |
rs762180422 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121384 | CAACAACAAAAAAAA[-/C]ATATAATACTTCTTT | 10277 |
rs762184205 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040034 | GATGGAGAAATGACA[C/T]CTTGGTTTCTAGCTA | 10277 |
rs762196691 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065753 | TCATTCTTTTCATCA[C/G]AAATTCTGTGAAAGA | 10277 |
rs762207116 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046852 | CTTTGATTGTAGACC[A/G]CGGACATTCCTCAGG | 10277 |
rs762224164 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076898 | ATTACAGGCGCCTGC[C/T]ACCACGCCTGGCTAA | 10277 |
rs762272601 | in-del | -/A | 1.66832e-05 | 0.00288814 | intron-variant | UBE4B | GRCh38.p7 | 1:10102902 | TGAAACACCTAACTC[-/A]ATACCTCTTATTTGA | 10277 |
rs762299071 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100020 | TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 10277 |
rs762322998 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112789 | TTCTTGTAAATCAGT[G/T]TTTGACCATTGACAC | 10277 |
rs762377431 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031113 | CTTTTTTTTTTGTGA[C/T]GGAGTCTCGCTCTGT | 10277 |
rs762379882 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032974 | CCTTTCAAAGATGGC[C/T]GCCCTGTTGTTTTGA | 10277 |
rs762390242 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154594 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 10277 |
rs762411164 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111505 | TATATAGAACACACA[C/T]GCACCCATGCACGCA | 10277 |
rs762423683 | snp | A/G | 3.30049e-05 | 0.00406219 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145005 | TGGCAACTAGACACC[A/G]CGAAATGCTGAAGCG | 10277 |
rs762430042 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080522 | TCCCTCAGAAAACTA[A/G]AAACAGAGCTACCAT | 10277 |
rs762439364 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124448 | CCACCTCGGCCTCCC[A/G]AAATGCTGGGATTAC | 10277 |
rs762474532 | snp | C/T | 3.4293e-05 | 0.00414069 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033639 | AACAGAAGGATCTCT[C/T]CTTAACGCCTTTCAC | 10277 |
rs762476505 | snp | C/T | 1.70939e-05 | 0.00292346 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106214 | TCTATGAAAGTAGTC[C/T]GGCTCCCACTCCCAG | 10277 |
rs762500508 | snp | A/G/T | 0.000231155 | 0.0107483 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178740 | AAATTTAAGCTGCTC[A/G/T]CCGAGAAAGTGGAGG | 10277 |
rs762525495 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043904 | CCTTCCAAACAATTA[C/T]ACTTAGATTCAGCAA | 10277 |
rs762528154 | snp | A/G | 1.84507e-05 | 0.00303727 | intron-variant | UBE4B | GRCh38.p7 | 1:10178608 | TTTTCCACCTGACGT[A/G]CATTTACGTCTCACA | 10277 |
rs762530657 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072180 | TCTCAATGTCCACAA[C/T]ATGACCCCAGCTACC | 10277 |
rs762532676 | snp | A/G | 4.98335e-05 | 0.00499142 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106407 | CACTCACCCATGGGC[A/G]TCCTCAGGCGTCTCC | 10277 |
rs762549981 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168383 | GGATCACAGTCATCA[A/G]TAAGTGAAATTCTGT | 10277 |
rs762555563 | snp | A/G/T | 3.30094e-05 | 0.00406249 | synonymous-codon, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149232 | GGTATTTGCAGCGTT[A/G/T]CCTGAGTTTTATGTA | 10277 |
rs762556749 | snp | C/T | 1.65037e-05 | 0.00287256 | intron-variant | UBE4B | GRCh38.p7 | 1:10129342 | TTATGCTACAAATGA[C/T]AGTCAGTTTAAGATG | 10277 |
rs762612503 | snp | A/G | 4.94246e-05 | 0.0049709 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072127 | CCTCCGGGGCCTCCC[A/G]TAGCGGCATCAGCCC | 10277 |
rs762615415 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094062 | TATTTTAAAGTATTT[A/G]CAAATGCCTGGGTAA | 10277 |
rs762624401 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060672 | TGTGGTCATCAGAAA[A/G]TAAGCCATTCTTTAA | 10277 |
rs762652537 | snp | C/T | 4.94442e-05 | 0.00497188 | intron-variant | UBE4B | GRCh38.p7 | 1:10147116 | TTCTTCCTGTTTCCC[C/T]TGTCCCTCCTTGGCT | 10277 |
rs762656712 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073576 | AAAAATACAAAAAGC[A/C]GGGTGTGGTGCTACC | 10277 |
rs762659515 | in-del | -/ATTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161902 | GATTGGCTTAGGTTT[-/ATTG]ATTCTGTTCTTGGAA | 10277 |
rs762667267 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089069 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 10277 |
rs762670012 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180266 | GTCTTTTAGTGATGG[-/C]TAATGGGTCTGGGCA | 10277 |
rs762683253 | in-del | -/TACCAGC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096920 | GTTGCATGCCTGTAG[-/TACCAGC]TACTTGGGAGGCTAA | 10277 |
rs762709650 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042250 | TAGTGGAAATGTCTT[-/C]CTGTAAACGGTTCAT | 10277 |
rs762731560 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130789 | GGTTAGCCAATCATT[A/G]CAGCATTACTTAGAG | 10277 |
rs762739345 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060176 | ATGCATCACTTAATG[A/G]CAGGGATACGTTCTG | 10277 |
rs762751440 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173837 | GTGGGTGGGCACAGC[A/C]CGCCCAGTGAGGTGA | 10277 |
rs762757901 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177891 | CCATTTTACACTCAA[A/G]GAACCTGGGCTTAGG | 10277 |
rs762775537 | snp | C/G | 4.9525e-05 | 0.00497595 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102951 | CTTCTTCACCAGGAG[C/G]CTTCCTCGGGCCCTG | 10277 |
rs762782502 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161395 | TGATATGCGATCTGA[C/T]ATGCTGGGATTTTCC | 10277 |
rs762793363 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161440 | ATTGCAGGATTGGAA[C/T]AGGAAAATTCTTAAA | 10277 |
rs762798481 | snp | C/T | 2.97314e-05 | 0.00385549 | intron-variant | UBE4B | GRCh38.p7 | 1:10135227 | CATTAAAACACTGCC[C/T]TCTTGTCTGTGTGCT | 10277 |
rs762798691 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158369 | AGATGTTGAGCATAC[C/T]GGAGCCACCAGTGAG | 10277 |
rs762805566 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116807 | AGGTTCTAGCTTCAG[A/G]TAACAAGTAAGCAGT | 10277 |
rs762822879 | snp | A/G | 1.66432e-05 | 0.00288467 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135112 | TTCACCCAAGATGTC[A/G]GATTACTCTTCCCAA | 10277 |
rs762850040 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126862 | CGACAGTGACTACTT[C/T]AAATACCCCCTCATG | 10277 |
rs762850856 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059014 | GCACTTTGGGAGGCC[A/G]GGGCGGGCGGATCAC | 10277 |
rs762855054 | snp | A/G | 1.67047e-05 | 0.00288999 | intron-variant | UBE4B | GRCh38.p7 | 1:10158534 | TTGCAAATCGCAGGT[A/G]GGATTGCAGCTTAAA | 10277 |
rs762863868 | in-del | -/TC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058642 | ACAGTCAGTGCTGCA[-/TC]CTGAGCCCACCAGCT | 10277 |
rs762901445 | snp | C/T | 3.32248e-05 | 0.0040757 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117564 | CCTCATCGAGTGTTT[C/T]GACCGAGTTGGAATA | 10277 |
rs762913984 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034874 | ATCAGGACTGCCCAT[G/T]CGGCGTTACTTTGTT | 10277 |
rs762923493 | in-del | -/AAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062974 | AAAAAAAAAAAAGAA[-/AAAG]AAAGAAAATAGTGAT | 10277 |
rs762932689 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038495 | TTCCTAATTTTACAA[A/G]TCAGGAAACTGGGAT | 10277 |
rs762938385 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129605 | AACTGTTACATTTTT[A/G]TTAGACACGTTATAT | 10277 |
rs762941681 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085068 | TTACGATTTTGAAAT[A/C]TTTGGATTCAGAAGA | 10277 |
rs762977750 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062199 | AGGCCTGAGCCACCA[C/T]ACCCGGCCCTATTTT | 10277 |
rs762988991 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130280 | GGGTTTCTCCATGTT[A/G]GCCAGGGTTGTCTCG | 10277 |
rs763038513 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155085 | AGAGAGAGAGAGAGA[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs763059897 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165163 | AATCAGTGTCTCAAA[C/T]TCACTGTGTCCAAAA | 10277 |
rs763067895 | in-del | -/AGTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062670 | CAAGAAAATAATGAT[-/AGTG]AGGCCAGGTGCGGTG | 10277 |
rs763077408 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088896 | TTTGCCCAGGTTGGT[C/T]TTAACCTCCTGGGCT | 10277 |
rs763079320 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | UBE4B | GRCh38.p7 | 1:10129495 | TCAGTGAATATATCA[C/T]AACCCAGAAGGCATT | 10277 |
rs763109112 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119200 | CTAGTCTTAAACTTC[C/T]GACCTCAAGTGATTT | 10277 |
rs763119608 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149853 | TGGTATGTGAAGTCT[A/G]TTGTGAAAAGTAAAA | 10277 |
rs763139246 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108025 | TTCATTTATCTATTG[C/T]GAGAATGTTATTGTG | 10277 |
rs763140567 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042517 | CCGGGCGTGGTGGTG[C/T]ACGCCTGTAATCCTA | 10277 |
rs763147311 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109293 | GACTCATGTTCACCA[C/T]CGCACCGTGCTGCCA | 10277 |
rs763160034 | snp | A/G | 9.90573e-05 | 0.00703696 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144995 | GATTCCCCACTGGCA[A/G]CTAGACACCGCGAAA | 10277 |
rs763170420 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120704 | TTAGCTGGGCATGGT[C/G]GCACGCACCTGTAAT | 10277 |
rs763186424 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178255 | CTTATAGGCTGCCAG[A/G]GCACAGTGCCCCCCA | 10277 |
rs763227945 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055694 | GGAGGCCAAGGTGGG[C/T]AGATCACTTGAGATG | 10277 |
rs763236079 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176319 | AACATTTGTGTAAAA[G/T]TATTTAAACACCTGT | 10277 |
rs763268894 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144074 | AAGGGGTTGAAATAG[C/T]GTTAAGAGAGTCGGT | 10277 |
rs763284661 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090476 | AGGAGGTCCTAAGGG[A/C]AGTTTTTAGACTCTG | 10277 |
rs763288790 | snp | C/T | 3.29598e-05 | 0.00405941 | intron-variant | UBE4B | GRCh38.p7 | 1:10130482 | GCGGCTTGACTGGCT[C/T]TTCCATCTTCTGCCT | 10277 |
rs763320102 | in-del | -/ACACACACAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166963 | CACACACACACACAC[-/ACACACACAAAA]AAAAAAAATTAGCTG | 10277 |
rs763344863 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131461 | CTGCACATCAGCCTG[G/T]GCGACAGAGCAAGAC | 10277 |
rs763364642 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127769 | ATACAGAAGCTAGGA[A/T]GACAAGGTCCCTCTC | 10277 |
rs763373243 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050799 | TCCAACTCCTGGCCT[C/T]AAGCCATCTTCCCTC | 10277 |
rs763411198 | in-del | -/T | 0.000118715 | 0.00770348 | intron-variant | UBE4B | GRCh38.p7 | 1:10072495 | ATGATTAAGACTGAA[-/T]TTGGTTCTGCTGATT | 10277 |
rs763427689 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165152 | AGTATTTGTCTAATC[A/T]GTGTCTCAAACTCAC | 10277 |
rs763434032 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081745 | AGGCACTGGCCACCA[C/T]GCCCAATTAATTTTT | 10277 |
rs763449526 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156100 | GTTCAACACAAGTCT[A/C]GTCCACCTACGGCCT | 10277 |
rs763452595 | in-del | -/AAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136924 | AAGTCCATCTCAAAT[-/AAAT]AAATAAATAAATAAA | 10277 |
rs763487097 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067764 | ATGGAGTCTCACTCT[A/G]TGGCCCAGGCTGGAG | 10277 |
rs763498318 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125820 | TTCCTTTAAGTGCCA[A/G]TAGCAGGTTAATGTA | 10277 |
rs763534948 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112838 | AAACTGGCCACTTTT[C/T]TTACTTGTGATCATG | 10277 |
rs763564193 | snp | C/G | 1.64841e-05 | 0.00287085 | intron-variant | UBE4B | GRCh38.p7 | 1:10147122 | CTGTTTCCCTTGTCC[C/G]TCCTTGGCTGGGCTC | 10277 |
rs763577866 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10099077 | AACCCTGTTTCCACT[-/AA]AAATACAAAAAAAAT | 10277 |
rs763580158 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034218 | TTTAACAAAATATGT[A/G]TCTTCTCCACAGTTT | 10277 |
rs763583195 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100472 | GCTCGGACCATAGGC[A/G]CATGCCAATATACCT | 10277 |
rs763587568 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114263 | TAGGTACAAGCCTGT[A/T]TTAGCAAAGTTCATC | 10277 |
rs763589067 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164868 | TTTTGAGCCTAGTGG[A/T]ATTTGGTATAATAAT | 10277 |
rs763606827 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146018 | GTTTACCTGACATAG[A/C]TTTCTAGTACCAGTT | 10277 |
rs763608761 | snp | C/G | 1.65701e-05 | 0.00287833 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106343 | GTGCAGCCTCTGGAA[C/G]TGCTGCGGGAAGCCA | 10277 |
rs763644993 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036818 | ATTGAAACTTCAAGC[G/T]TATATTTCAGGGTTA | 10277 |
rs763653818 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147029 | TTCCTGAGAAGATGT[C/G]TGAATTTTTATGGCC | 10277 |
rs763667438 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056132 | ATGCAGTTAAAATTA[C/T]TCTACACTCAGCATG | 10277 |
rs763677300 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132742 | GTAGGTACCAGAAGG[A/G]AGATCTGAAGGTGAT | 10277 |
rs763684183 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064407 | CGAGGAATTGTAGTA[C/T]TTCTATGCATACGTG | 10277 |
rs763688222 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130804 | GCAGCATTACTTAGA[A/G]CTCGGAAGGGTAAGT | 10277 |
rs763713146 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091026 | AACTCTTCTCAGTTA[C/T]AGAAGTTGGATACTG | 10277 |
rs763723587 | snp | C/T | 0.000237501 | 0.0108947 | intron-variant | UBE4B | GRCh38.p7 | 1:10072505 | CTGAATTTGGTTCTG[C/T]TGATTTTATGAATTT | 10277 |
rs763724680 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144459 | AGAAAAATATGGCCC[A/G]ACGCAGTGGCTCATG | 10277 |
rs763727425 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057533 | GCGCTTCTCCTGCCT[C/G]AGCCTCCTGAGTAGG | 10277 |
rs763757309 | snp | C/T | 6.59914e-05 | 0.00574381 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10102958 | ACCAGGAGCCTTCCT[C/T]GGGCCCTGAAGTGTC | 10277 |
rs763813309 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158015 | GTATGTCCATTTGAG[A/G]TGCCATAGAATTTCT | 10277 |
rs763825614 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127880 | GAGCTGTACACAAAG[A/G]GTGTATTTATCTATT | 10277 |
rs763856003 | snp | A/C/T | 3.58027e-05 | 0.00423087 | intron-variant | UBE4B | GRCh38.p7 | 1:10126755 | CCACTCTTAGATTCT[A/C/T]TTAAACTTATATTTC | 10277 |
rs763905891 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115096 | AAATTTACTAGACTC[C/T]GGGCTGAACGCCTTG | 10277 |
rs763915152 | snp | C/T | 1.66729e-05 | 0.00288724 | intron-variant | UBE4B | GRCh38.p7 | 1:10161098 | GCTGTGGCATTTTGC[C/T]TCAGGGAGATGTATG | 10277 |
rs763926732 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126176 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTGGCT | 10277 |
rs763963027 | in-del | -/TTTTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176685 | CTGGCCATTTTTATA[-/TTTTC]TTGGGAGCAATGTCT | 10277 |
rs763965334 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115163 | TACTTTAATACCATA[-/C]CTTTTTTTTTTTTTT | 10277 |
rs763968274 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082085 | TATGTTGGTTGTTAC[A/G]TTGATTTATTGAATG | 10277 |
rs763969303 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156847 | TTTTTGGTCACACAC[-/A]AAAAAAATGTGTTCT | 10277 |
rs763970278 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096526 | CACTTGAGGTCAGAA[G/T]TTCAAGACCAACCTG | 10277 |
rs763998464 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081809 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 10277 |
rs764023073 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083779 | TGAGTTGGAACAGGT[A/G]TGTCCTATGCTGGCA | 10277 |
rs764029017 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109280 | CATCCTGAATCCAGA[C/T]TCATGTTCACCACCG | 10277 |
rs764041858 | snp | A/T | 3.14056e-05 | 0.00396255 | intron-variant | UBE4B | GRCh38.p7 | 1:10135233 | AACACTGCCCTCTTG[A/T]CTGTGTGCTAGTAGT | 10277 |
rs764060262 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095375 | ATGATGGGTGACTGC[A/G]GATTGTGCGTGTTTA | 10277 |
rs764065405 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126869 | GACTACTTTAAATAC[C/G]CCCTCATGGTAAAAC | 10277 |
rs764089127 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161999 | TTTCTTCACTTTTTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs764094463 | in-del | -/CTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173310 | GGTGAAACCCCGTCT[-/CTA]CTAAAAAAAATACAA | 10277 |
rs764104919 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055484 | CACACCCAGCTAATT[A/T]AAAAAATTTTTTTTG | 10277 |
rs764145483 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086334 | GCTTGTGTTGAACTC[C/G]TGACCTCAGGTGATC | 10277 |
rs764148328 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10170161 | ATCTGGCCTTTGCAG[A/G]CAAAGTGTAAAGGCA | 10277 |
rs764163782 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131738 | CAGGTGGATCACGAG[G/T]TCAGCAGTTTGAGAC | 10277 |
rs764194818 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085622 | CAACAACACATCTTT[A/C]TAACTTTAATGCAAC | 10277 |
rs764198934 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175286 | AGACTGCATATCTGT[C/T]GTCCATGAAGCATTG | 10277 |
rs764202522 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072377 | AATGTGTTGTGTTAT[C/T]GCTTTTTTTTTTATT | 10277 |
rs764202591 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087094 | TCTCATTCTGTTCTC[A/G]TCTGACGCATACAGG | 10277 |
rs764299121 | in-del | -/CACACACAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166964 | ACACACACACACACA[-/CACACACAAA]AAAAAAAAATTAGCT | 10277 |
rs764299313 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117705 | TCAGTAAAGCAATTA[C/T]TGAGCATTTGCCATG | 10277 |
rs764311959 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099589 | TTTTGGTCAAAATCC[C/T]GGGAGGGTTTTTAAG | 10277 |
rs764362658 | snp | A/T | | | intron-variant, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170355 | CTTGAAAAGCTAAGT[A/T]TATGTTGAATTTGTA | 10277 |
rs764368845 | snp | A/G | 3.30513e-05 | 0.00406504 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178777 | TGGCCAAGAACGCAC[A/G]CGCAGAAATCGACTA | 10277 |
rs764379028 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050995 | AGTCAGACATACTTG[C/G]AGGCTTTTTTGGTTG | 10277 |
rs764384666 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031006 | GTGAAGGAAGCCAAA[C/T]CCCAAAGGCCACACG | 10277 |
rs764388221 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098391 | GAACAGAAAGGAGTA[G/T]CTTTAAACTCACAGT | 10277 |
rs764396874 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153159 | TAGAGAGGGCGGGCT[A/G]CCAAAGGAAAGATTC | 10277 |
rs764397908 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038729 | TGCATGAATGCATTC[A/C]TGATGTGATCAGGGC | 10277 |
rs764423623 | snp | A/G | 1.7857e-05 | 0.002988 | intron-variant | UBE4B | GRCh38.p7 | 1:10178864 | TCTTTTGAGTTAACT[A/G]GAAATCGATAACATT | 10277 |
rs764434075 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052676 | GTAGCCTGCATATTC[A/T]TTTGTCATGGGGCCC | 10277 |
rs764462710 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127333 | TCTCTTGTTCACCCT[-/C]CCTGTTTCCTAAGGT | 10277 |
rs764465279 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132443 | TCTCAGTTACATGGC[A/G]GCTGTCGTCAATGCC | 10277 |
rs764484000 | snp | A/G | 8.25962e-05 | 0.00642583 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179965 | TCACTAAACCGTTCC[A/G]CCGCCCACCCTCTGC | 10277 |
rs764523241 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078794 | ATAGGTCTTCCAGTG[C/G]AATAGGTCTGCCTGT | 10277 |
rs764539041 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111410 | CGGACCACTCTCCCC[A/G]CTAGACAGCTGTATG | 10277 |
rs764605475 | snp | A/G | 6.58924e-05 | 0.0057395 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137166 | TGCCTAGTTGCCGTC[A/G]CTATATCCGCAGACT | 10277 |
rs764607080 | snp | A/G | 1.65974e-05 | 0.0028807 | intron-variant | UBE4B | GRCh38.p7 | 1:10168129 | GCGTCTGTTCGATGT[A/G]TCCTAGGATCAGCAG | 10277 |
rs764615976 | snp | A/G | 1.681e-05 | 0.00289909 | intron-variant | UBE4B | GRCh38.p7 | 1:10103120 | CTCAGCAGTCTTACT[A/G]CAGAGTACTCGACAA | 10277 |
rs764620150 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064845 | CTCTGCTCACTGCAG[C/T]CTCCACCTCCCGGGT | 10277 |
rs764622230 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119554 | GCTTCTGAGCAACAT[C/T]CGCTCACAGTGCATA | 10277 |
rs764630803 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121090 | TATAATACGGCCAGG[C/T]GTGGTGGCTTACATC | 10277 |
rs764666467 | snp | C/G | 7.20474e-05 | 0.00600154 | intron-variant | UBE4B | GRCh38.p7 | 1:10126745 | GACATACTTCCCACT[C/G]TTAGATTCTCTTAAA | 10277 |
rs764673121 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105553 | GATTGGCCAGATTTT[A/G]ATGGAAGTGCTAATG | 10277 |
rs764690277 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171230 | AGTTGAAAACCCTGA[G/T]AAATACGGCTTTGAA | 10277 |
rs764713982 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063493 | TAACAGCCAAGTTCT[A/G]TTGGGAACACAGATC | 10277 |
rs764719811 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149000 | TACCCTTGCATATGC[A/G]CTGTCTTCATTATTC | 10277 |
rs764768784 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167147 | AAAAAAAAATAACAA[C/T]AATAATAGAGGGCCG | 10277 |
rs764778044 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072112 | CCCCAGAGGGAGAAC[C/T]CTCCGGGGCCTCCCA | 10277 |
rs764797641 | snp | A/C | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126849 | AAGAGTGCTCCCTCG[A/C]CAGTGACTACTTTAA | 10277 |
rs764841815 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078880 | GGAGTACAGTGGTGC[A/G]ACCATAGCTCATTGC | 10277 |
rs764894738 | snp | G/T | 1.8704e-05 | 0.00305805 | intron-variant | UBE4B | GRCh38.p7 | 1:10106598 | GGTATTTATCCCACA[G/T]GAGAGTTGCATGTGT | 10277 |
rs764933335 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118035 | ATAACATAGGCATTC[-/T]TTTTTCAACGTATGA | 10277 |
rs764937209 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151462 | ATGTTTATGACCAAC[C/T]CTGCTGTTCAGCCAC | 10277 |
rs764942589 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038170 | CTGTGATCCGAGGTA[C/T]TCAGGAGGCTGAGGC | 10277 |
rs764953820 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146179 | TTAAATTGCCAGGCA[A/T]GGTGGCTCACACCAG | 10277 |
rs764967946 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116737 | GTATAGACTGCTGAT[A/G]TTTTACAAAGCACCT | 10277 |
rs764986947 | snp | A/G | 2.04384e-05 | 0.00319668 | intron-variant | UBE4B | GRCh38.p7 | 1:10134961 | TTTTTAATGTTTAAA[A/G]ATACTTTTTCTTTTC | 10277 |
rs765004153 | snp | C/T | 8.23662e-05 | 0.00641688 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147007 | TGCTGGCCTACTTGA[C/T]GAGAGCTTCCTGAGA | 10277 |
rs765005672 | snp | A/G | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10146964 | CCCTGCTTCCACAGA[A/G]ACTGGTACGGTGCAA | 10277 |
rs765010316 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058974 | GCATGCCGGCTGGGC[A/G]CGGTAGCTTGTGCCT | 10277 |
rs765012348 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175641 | GGGCGACAGAGCGAG[A/G]CTCCGTCTCAAATAA | 10277 |
rs765028845 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113232 | GGATGTCCCAGACTC[-/TT]TTAAACAACCAGATC | 10277 |
rs765044252 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083886 | AGCATTATTCCTAGG[A/G]TCATACTAATTACTT | 10277 |
rs765046926 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116087 | GTTTCTAGACATTAA[C/T]TGTGTGTCCTGGGTT | 10277 |
rs765057375 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058636 | TGACCACAGTCAGTG[-/A]CTGCATCCTGAGCCC | 10277 |
rs765071903 | snp | C/T | 1.65326e-05 | 0.00287507 | intron-variant | UBE4B | GRCh38.p7 | 1:10095622 | GCCAGTTTTCTAATA[C/T]GCTCTTTTATTTAGG | 10277 |
rs765118779 | snp | A/G | 1.66502e-05 | 0.00288527 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179448 | CTCATGACAGACCCC[A/G]TGCGGCTGCCCTCTG | 10277 |
rs765141487 | in-del | -/GAAGCTTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074244 | GTCCCTGCTGCTGTT[-/GAAGCTTG]GACCCTAGATCCCAT | 10277 |
rs765141794 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048898 | TGAGCTTATCTTTTT[C/T]TGTTTTAACTTTTCC | 10277 |
rs765162871 | in-del | -/C | 2.88023e-05 | 0.00379477 | intron-variant | UBE4B | GRCh38.p7 | 1:10135225 | GTCATTAAAACACTG[-/C]CCTCTTGTCTGTGTG | 10277 |
rs765185454 | snp | C/T | 1.67517e-05 | 0.00289406 | intron-variant | UBE4B | GRCh38.p7 | 1:10103110 | AGGAATCTAGCTCAG[C/T]AGTCTTACTGCAGAG | 10277 |
rs765188109 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070626 | TTTTTACATCTGGCT[G/T]CTTTTGCTCAGGGGA | 10277 |
rs765216150 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170468 | GCTCTCTAAGCCACA[C/T]CTTCCTGTTTCAGGT | 10277 |
rs765219620 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158148 | TTCCTTTAGGTGTTG[G/T]GTCATTGTCAAATCT | 10277 |
rs765221276 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172283 | TCTGCCTCATTTTCA[A/C/G]CGTCCTCACAGCTAA | 10277 |
rs765234594 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084879 | ATTTTTTTTTTTGTA[A/T]TTTTAGTTGAGACAG | 10277 |
rs765248938 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135102 | ACGTATATTTTTCAC[C/T]CAAGATGTCGGATTA | 10277 |
rs765278053 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069637 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 10277 |
rs765315386 | snp | A/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072153 | AGCCCCAGGACCCTC[A/T]CAGAGTCTTGGTCTC | 10277 |
rs765364204 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148719 | CCAAGATGGGTGGAT[C/T]ACTTGAGGTCAGGAG | 10277 |
rs765366850 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060524 | TTTCCTCTCTGACTT[C/T]CCCAGGAGAGCTGGT | 10277 |
rs765367588 | snp | A/C | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105522 | TTCCAACAGTATTCT[A/C]CGATTTTAAGGACTT | 10277 |
rs765371392 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110325 | TTGCAGACTTCTGAG[-/A]AAAGAACTGTTTGAG | 10277 |
rs765374099 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041554 | GGCCAGGCTGGTCTC[-/G]GAACTTCTGACCTCA | 10277 |
rs765404233 | snp | C/G/T | 4.94192e-05 | 0.00497067 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137162 | ATTCTGCCTAGTTGC[C/G/T]GTCGCTATATCCGCA | 10277 |
rs765414274 | in-del | -/TCC | 1.66679e-05 | 0.00288681 | intron-variant | UBE4B | GRCh38.p7 | 1:10179872 | CATCTGGGGCATTAA[-/TCC]TCCTTTTTTTCTTTT | 10277 |
rs765418577 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149759 | AAATTAACATTTTAT[G/T]TCTAAAACATTACAG | 10277 |
rs765425754 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077181 | GAAGTCCAAAGCCAA[G/T]GTGTTGGTAGGGCGA | 10277 |
rs765456814 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074530 | TGCCCTTGCACTCTT[C/T]GCTGAATCAACTGCA | 10277 |
rs765477824 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044734 | CATAGGCGCACGCCA[-/T]TCATGCCCGGCTAAT | 10277 |
rs765477993 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053965 | GTGCTGGGATTACAG[A/G]TGTGAACCACCATGT | 10277 |
rs765519550 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100028 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10277 |
rs765526877 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | UBE4B | GRCh38.p7 | 1:10129374 | AATGCATTTAAATGA[C/T]TCTGATCTTATTTCT | 10277 |
rs765532827 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142469 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 10277 |
rs765534470 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040241 | GTGATTCTCCTGCCT[C/T]AGCCTTCCAAGTAGC | 10277 |
rs765551713 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117804 | CTCACATTCTAATAG[A/C]GACAGAGCCAAGGTT | 10277 |
rs765589911 | snp | C/G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143335 | TCAACCCGGGAGTCA[C/G/T]AGGTTGCAGTGAGCC | 10277 |
rs765611987 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080554 | TGATCTGGCAGTCCC[A/T]CTGAGTATATATCCA | 10277 |
rs765627203 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | UBE4B | GRCh38.p7 | 1:10130658 | GCTGCCCTTTTATTC[A/G]GATTCTTTCCCAAAT | 10277 |
rs765634467 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062344 | TTGAGGTGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 10277 |
rs765648505 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144733 | GCGAGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA | 10277 |
rs765665210 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065866 | ATAATGTAAATCTAC[A/G]TCCTTTTAAAAAATA | 10277 |
rs765688545 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112809 | ACCATTGACACTTAA[C/G]GCTTGTATTAGTGAA | 10277 |
rs765689091 | snp | C/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117475 | TTGGGAGCCTCTGGT[C/G]GAGCAAGTAATTGGG | 10277 |
rs765689895 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant | UBE4B | GRCh38.p7 | 1:10179608 | CTGGCGTCAGTACCA[A/G]GAGATAAAGCCCAAG | 10277 |
rs765725936 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065220 | TATTTGAAAGTATGG[A/G]GAACCACTAAAGCAG | 10277 |
rs765741134 | snp | C/G | 1.65332e-05 | 0.00287512 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179933 | CAGGCGTGGATGAGA[C/G]AGAAACAGAACAGCG | 10277 |
rs765745050 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161121 | GATGTATGACCATGT[A/G]CAATATAATTGCCTT | 10277 |
rs765748197 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094875 | GGCTCACTGCAACGT[C/G]TTCCTCCCAGATTCA | 10277 |
rs765751703 | snp | C/T | 4.94238e-05 | 0.00497086 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130771 | CCTGGAAAACACTCG[C/T]GTGGTTAGCCAATCA | 10277 |
rs765764633 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031123 | TGTGACGGAGTCTCG[C/T]TCTGTTGCCCAGGCT | 10277 |
rs765808591 | snp | G/T | 2.21722e-05 | 0.00332951 | intron-variant | UBE4B | GRCh38.p7 | 1:10134955 | AAATTTTTTTTAATG[G/T]TTAAAAATACTTTTT | 10277 |
rs765871261 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154667 | AAAATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10277 |
rs765908151 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094069 | AAGTATTTGCAAATG[C/T]CTGGGTAAACATTCT | 10277 |
rs765917963 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105709 | AAGCCCCATGTTCTG[C/T]AGCGTGGCTTCCTTT | 10277 |
rs765921173 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169797 | AGAAGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 10277 |
rs765924382 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058645 | GTCAGTGCTGCATCC[A/T]GAGCCCACCAGCTGC | 10277 |
rs765939094 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112943 | TTCCTGTTTGGTTAA[A/T]GCTTTGTTTAACTCC | 10277 |
rs765951687 | snp | A/G | 1.64787e-05 | 0.00287038 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101163 | GAGGTTGATGAAAAT[A/G]ATCGAAGAGAAAAGC | 10277 |
rs765983079 | snp | A/G | 1.69192e-05 | 0.00290849 | intron-variant | UBE4B | GRCh38.p7 | 1:10122104 | GAGTTTGCTCTTGCA[A/G]ATTTTAGCCTGAGAG | 10277 |
rs765985461 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180531 | GATCGTATTTTTATA[C/T]CATATTCACATATTT | 10277 |
rs766110287 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060183 | ACTTAATGACAGGGA[C/T]ACGTTCTGAGAAACG | 10277 |
rs766124861 | snp | C/G/T | 3.51508e-05 | 0.00419218 | intron-variant | UBE4B | GRCh38.p7 | 1:10149327 | TAATATGTTTTTATG[C/G/T]ATAATAGTATAATAT | 10277 |
rs766135114 | snp | C/T | 9.40672e-05 | 0.00685746 | intron-variant | UBE4B | GRCh38.p7 | 1:10106615 | AGAGTTGCATGTGTG[C/T]TTGCGGTGCAGGGAA | 10277 |
rs766149032 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046404 | TTAGTTTAAAACAAA[A/G]TTATCAGGGGCTCTG | 10277 |
rs766168345 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135553 | ACCAGCCTGATCACC[A/G]TGGTGAAACCCCATC | 10277 |
rs766168412 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147956 | GTGTAGGCCGGGTGC[A/G]GTGGCTCACGCCTAT | 10277 |
rs766174169 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070851 | CTACAAGTGATGGTT[A/G]AATTTGTGTCTTAGT | 10277 |
rs766204778 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159181 | ATTTTGCAACAATTA[G/T]GTCAGAGTTGTCATT | 10277 |
rs766232472 | snp | A/G | 1.73081e-05 | 0.00294172 | intron-variant | UBE4B | GRCh38.p7 | 1:10178842 | ACTCGTCGTTTTCAT[A/G]CTGATTTCTTTTGAG | 10277 |
rs766244666 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093198 | TTTACTACCATAATG[A/T]TCATTGAAGTTTATT | 10277 |
rs766274749 | snp | A/G | 2.39317e-05 | 0.00345909 | intron-variant | UBE4B | GRCh38.p7 | 1:10117647 | AAAGCCTAGTTATTT[A/G]TTTGATTATCCCCAC | 10277 |
rs766275620 | in-del | -/TACG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154019 | CCGCGAGGCAGAGGT[-/TACG]TACGGTGAGCCAAGA | 10277 |
rs766277757 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038521 | GGGATTCAGGTTAAG[G/T]AACTTGTCCATAGCG | 10277 |
rs766310906 | snp | A/G | 3.30879e-05 | 0.00406729 | intron-variant | UBE4B | GRCh38.p7 | 1:10117409 | AATGCAAACTCTGCC[A/G]AAAATAATCAAGAGA | 10277 |
rs766316190 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173863 | GGTGATGCAAAGCAA[C/T]TGGGTGACAAAGGAA | 10277 |
rs766324646 | snp | A/G | 1.7127e-05 | 0.00292629 | intron-variant | UBE4B | GRCh38.p7 | 1:10132498 | GTAGGATTCCTACAG[A/G]CTGCTTTTCGCTGTT | 10277 |
rs766340305 | snp | A/C | 1.74683e-05 | 0.00295531 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106527 | GGGTCCACCCCTACC[A/C]CCCGCCTCACCCAGT | 10277 |
rs766348080 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059036 | GCGGATCACGGATCA[C/T]CTGGCCAACATGGTG | 10277 |
rs766365583 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155709 | CTTAACACCACAGAG[-/AT]AGTATTCTAGCTTAG | 10277 |
rs766368360 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158425 | ATCATATTAGCACCA[C/T]TTTTAAAAGCCTTTG | 10277 |
rs766390760 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077635 | GGAAATGTTAGAAGC[A/G]AAGTAAGATTTGAGT | 10277 |
rs766394006 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105816 | AGGAGAAGGGAATGT[G/T]TGTTGACAGTGTTAA | 10277 |
rs766399484 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095586 | ATCGATGGTGTCTCA[C/T]GTGAGAAAAGGTAAA | 10277 |
rs766406027 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160591 | GCACTTGACTGTCAT[A/C]AGCCGTGCAAGGTGG | 10277 |
rs766413400 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096644 | GGAGAATCACTTGAA[C/T]CCAGGAGGTGGAGGT | 10277 |
rs766423496 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063222 | GCAGTGAGCTGAAAC[C/T]GTGCCTCTGCACTCC | 10277 |
rs766435445 | in-del | -/ACAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039080 | CAAACAAACAAAAAA[-/ACAC]ACACACAGAAAAACA | 10277 |
rs766458510 | in-del | -/AAGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116812 | CTAGCTTCAGGTAAC[-/AAGT]AAGCAGTGGGGTTGA | 10277 |
rs766461451 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037081 | GCCCAGGCTGGAGTG[-/C]CAATGGCGCGATCTT | 10277 |
rs766473996 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174727 | AAAAAAAAAAAGTGT[C/T]TTTGCTTCCTTTCAC | 10277 |
rs766478241 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138723 | TCCATCTTGTTTCAG[C/T]TGGTGGAGGAAAGCT | 10277 |
rs766515234 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047939 | TACAGTGCAGCCTCT[A/C]ACTCCTGGGTTCAAG | 10277 |
rs766516955 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138633 | ACAATTTTATTTCTT[C/T]TACTTTTTTTTTCAT | 10277 |
rs766516958 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10151762 | ACAACCATTCCACCT[A/G]CTGGTCTCTGATGAT | 10277 |
rs766532616 | snp | A/C | 1.66241e-05 | 0.00288302 | intron-variant | UBE4B | GRCh38.p7 | 1:10161117 | GGGAGATGTATGACC[A/C]TGTACAATATAATTG | 10277 |
rs766535640 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120847 | TCTCAAAAAATAATA[A/C]TAATACTAAATAAAT | 10277 |
rs766569889 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139798 | CAATGGTGCAATCTT[A/G]GCTCACCTCAACCTC | 10277 |
rs766572820 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051116 | GGCTCAGATGATTTT[C/T]CCGCCTCAGCCTCCT | 10277 |
rs766577206 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165167 | AGTGTCTCAAACTCA[C/T]TGTGTCCAAAACGGA | 10277 |
rs766599998 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042572 | GAATAGCTTGAACCC[A/G]GGAGGCAGGGGTTAC | 10277 |
rs766629409 | in-del | -/GAAGAAGATGAA | 0.000161538 | 0.0089857 | intron-variant, cds-indel | UBE4B | GRCh38.p7 | 1:10107280 | GGGGACAGTAGTGAT[-/GAAGAAGATGAA]GAAGAAGATGATGAT | 10277 |
rs766682593 | in-del | -/AT | 0.000128692 | 0.00802056 | intron-variant | UBE4B | GRCh38.p7 | 1:10132319 | AGTCAAAAAGGAATC[-/AT]GTGCAAAATAGTTTT | 10277 |
rs766702266 | snp | G/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145023 | AAATGCTGAAGCGCT[G/T]TAAAACTCAGCTTAA | 10277 |
rs766718054 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041720 | GTTTGTTTTTTAAGA[C/T]AGAGCCTCGCTGTGT | 10277 |
rs766730674 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114326 | TATGAATGTTAGCAG[C/T]AGAGGAGGGATCGCA | 10277 |
rs766739938 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant | UBE4B | GRCh38.p7 | 1:10137024 | TTTCTCTGATTGAGA[C/T]ATGTAATAGATTTTA | 10277 |
rs766754424 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090126 | CCTGTGTGTGTGTGT[-/G]GTTTTTTTTTTTAGG | 10277 |
rs766757398 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058659 | CTGAGCCCACCAGCT[-/G]CCGCCTGCAGGTGGG | 10277 |
rs766773664 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036206 | CAGTGAAGATATTGT[A/G]TAATCTAAAATGTGT | 10277 |
rs766800561 | snp | C/T | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132445 | TCAGTTACATGGCGG[C/T]TGTCGTCAATGCCAA | 10277 |
rs766812302 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179515 | TGCTCAACTCCCCCA[C/T]GGACCCCTTCAACCG | 10277 |
rs766821574 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054371 | CTTTGGGCGAGGGGA[C/T]ACCACACTTCTACTC | 10277 |
rs766825304 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | UBE4B | GRCh38.p7 | 1:10130637 | TATAGTGGCTACTTG[C/T]ACTTTGCTGCCCTTT | 10277 |
rs766857483 | in-del | -/GGTGACCTTCTCA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057972 | GACTGTCGGATGTGG[-/GGTGACCTTCTCA]GGTCATGTCCACACA | 10277 |
rs766862120 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143415 | AAAAAAAAAAGACAA[C/T]AACAAGATCTCCTTC | 10277 |
rs766864350 | in-del | -/TGTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065139 | TTGTTACATTCACTT[-/TGTC]TGTATATAAATGTGT | 10277 |
rs766882258 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053025 | GTCATCAGGGGTTCC[A/G]CCCTCAGGACCTCAT | 10277 |
rs766896134 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10146999 | TGTGCTGATGCTGGC[C/T]TACTTGACGAGAGCT | 10277 |
rs766908060 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165198 | ACCCTTGATGTTGTC[-/CA]CATCTCCTGCCTGAG | 10277 |
rs766942302 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095573 | CCAGAGCATGGATAT[C/T]GATGGTGTCTCATGT | 10277 |
rs766950922 | snp | C/T | 1.70737e-05 | 0.00292174 | intron-variant | UBE4B | GRCh38.p7 | 1:10149311 | ATATTTTACATAGTT[C/T]TAATATGTTTTTATG | 10277 |
rs766981038 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100663 | GAGTTCAAGTGATTC[-/T]GCTGCATCAGCCTGC | 10277 |
rs766995114 | snp | A/G | 3.31691e-05 | 0.00407228 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132471 | GCCAATATGAAGAAA[A/G]CACAGATGCAGGTAG | 10277 |
rs767005128 | snp | A/G | 0.000124355 | 0.00788429 | intron-variant | UBE4B | GRCh38.p7 | 1:10072550 | AGATAAAATAATCTG[A/G]AAATGCAAGATTAAA | 10277 |
rs767041968 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081907 | ATTTGTGCAGACAAG[C/T]TCTCACTATGTTACC | 10277 |
rs767049921 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114867 | AGACTCCATCTCAAA[A/G]AAAAAGACACAATAA | 10277 |
rs767062260 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131677 | AGTCATCCTGGCCAA[C/G]ATGGTGAAACCTCGT | 10277 |
rs767075916 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157892 | TAATAGATTTAGGGA[C/T]GATAGACACATTGGT | 10277 |
rs767088023 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143573 | ATCTCAAATCCATAC[C/G]CTTAATCACATCTAC | 10277 |
rs767100076 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126083 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGTTCGA | 10277 |
rs767103054 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101433 | GGCCATGATTTTATC[A/G]GTAAATTTAGGTTGT | 10277 |
rs767123373 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069326 | GCAGATATTTAGAGA[A/G]TACCTACCATGTGTC | 10277 |
rs767152344 | in-del | -/AAAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136941 | AATAAATAAATAAAT[-/AAAC]AAATAAAAAGTATCT | 10277 |
rs767229317 | snp | C/T | 1.65211e-05 | 0.00287407 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179964 | ATCACTAAACCGTTC[C/T]GCCGCCCACCCTCTG | 10277 |
rs767281851 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136775 | AAATGCAAAAGTAGC[C/T]AGGTGTGGTAGCACA | 10277 |
rs767307145 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034292 | ACTTCTGGCATTCTT[C/T]TGTTACATTCTATCT | 10277 |
rs767332424 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081453 | TTATTTTGAGATGGT[C/T]CCACTCTGTCACCCA | 10277 |
rs767332727 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124525 | CAGAATTCTGCTGAC[C/T]TTTCAGCCACTCAGT | 10277 |
rs767341324 | snp | C/T | 1.75265e-05 | 0.00296023 | intron-variant | UBE4B | GRCh38.p7 | 1:10178635 | CACATTGCCATTCCT[C/T]CTTTGCAGAGATCCT | 10277 |
rs767351956 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137154 | ACCTCTCTATTCTGC[C/T]TAGTTGCCGTCGCTA | 10277 |
rs767397421 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080809 | GAAATAAGCCAGGCA[C/T]AGAAAGGCAAATATT | 10277 |
rs767398257 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175555 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 10277 |
rs767417302 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107945 | AATCATTTTTCAAAA[A/G]CATGAAAACAGATTA | 10277 |
rs767458720 | snp | A/G | 3.32358e-05 | 0.00407637 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106417 | TGGGCGTCCTCAGGC[A/G]TCTCCATTCTGTCGA | 10277 |
rs767467963 | snp | A/C | 3.30196e-05 | 0.00406309 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178756 | CCGAGAAAGTGGAGG[A/C]GATAGTGGCCAAGAA | 10277 |
rs767468629 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095259 | CTCATATGAAGTATA[A/T]TGATAACTTATGATT | 10277 |
rs767473527 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141231 | CTTGATTAAAGGGAC[C/T]TTGCAGCTGTGATAT | 10277 |
rs767476743 | snp | A/G | 1.64939e-05 | 0.0028717 | intron-variant | UBE4B | GRCh38.p7 | 1:10129354 | TGACAGTCAGTTTAA[A/G]ATGAAATGCATTTAA | 10277 |
rs767477329 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061912 | TTATCTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs767495636 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060470 | AAGATCTGGTGATCT[A/G]ACATTGACTGAAATG | 10277 |
rs767518365 | in-del | -/AAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134059 | TGTCTCAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 10277 |
rs767520755 | in-del | -/AGTGTGCATGGTGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051317 | ATTGGAGTGATGTGA[-/AGTGTGCATGGTGT]AGTGACCTGGCCGAG | 10277 |
rs767557265 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050602 | CTCCTGGCTATTCTT[A/G]TTTACTGCTTTTTAT | 10277 |
rs767592398 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154786 | GGCAGAGGTTGCAGT[-/G]AGCCAAGATCGTGCC | 10277 |
rs767592759 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034591 | CCTTTCAGGACCCCT[-/A]ACTGGCCATACCCTC | 10277 |
rs767633585 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099518 | ATACTTGGAGAGTAA[G/T]GAAAACTCAGTAATA | 10277 |
rs767641100 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064619 | TTCCACTCTCTATCA[C/T]CTCGTCTCTTTGTCA | 10277 |
rs767652047 | snp | A/C | 1.87675e-05 | 0.00306324 | intron-variant | UBE4B | GRCh38.p7 | 1:10106608 | CCACAGGAGAGTTGC[A/C]TGTGTGTTTGCGGTG | 10277 |
rs767659841 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096980 | GGAGGTGTAGGCTAC[A/C]GTGAACTGAGATCAC | 10277 |
rs767660179 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110200 | CAGTGGATTCGATGT[A/C]TTATAAATCTTTTTG | 10277 |
rs767666737 | snp | A/G | 1.65021e-05 | 0.00287241 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072058 | CTTGCACGACTTGCT[A/G]GTGGACAGACCTCTC | 10277 |
rs767677267 | snp | A/G | 1.65833e-05 | 0.00287948 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179479 | GCACCATCATGGACC[A/G]CTCCATCATCCTGCG | 10277 |
rs767687023 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128361 | GGACACAGTGAGTGA[A/G]AGGGTACAATAATGA | 10277 |
rs767690032 | in-del | -/AAAAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055926 | CTGTCTCAAAAAAAC[-/AAAAC]AAAACAAAACAAAAC | 10277 |
rs767734462 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063433 | CATTTAGGTATCCAG[A/G]CCTGAAATCTAGATT | 10277 |
rs767740378 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129666 | TTTTTCCCTTTTTTT[C/T]CTAAGAATCTCACTC | 10277 |
rs767743479 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120996 | CAAAACTTTAAAAAA[C/T]GTTCCTTGATTAAAA | 10277 |
rs767755258 | snp | C/T | 1.67214e-05 | 0.00289144 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10101208 | AAGGTTGGTAAGCGA[C/T]GAAGCCCTTGGTACA | 10277 |
rs767791672 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049091 | TGGGGAACATTGGAT[C/T]ATATTATAGTTTTTA | 10277 |
rs767794530 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100855 | CACTGCACTCGGCCA[A/G]TGATATACTTTTAAA | 10277 |
rs767806511 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143661 | TGCGACAAGTTTGGA[-/G]GAGCCATTCTTTTGT | 10277 |
rs767824895 | snp | A/C | 1.66971e-05 | 0.00288934 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168249 | CCTCACGAAGCAGGT[A/C]CAGAAGCCCTTCCTC | 10277 |
rs767849449 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140064 | GAGATGGATATTTAG[A/G]TCATCCTTTCCAACC | 10277 |
rs767876004 | snp | C/T | 1.68946e-05 | 0.00290638 | intron-variant | UBE4B | GRCh38.p7 | 1:10121916 | TTTCACGTGCCTCTG[C/T]AGTGAGTTGACTTCA | 10277 |
rs767888686 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180414 | CTTGCACTGCTGTGG[A/C]TTTTTTTAAGAGAAG | 10277 |
rs767892476 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155086 | AGAGAGAGAGAGAGT[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs767919109 | in-del | -/AGTT | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099350 | CTGCCAGCAACAAAA[-/AGTT]AGAAAACGTAATTTT | 10277 |
rs767921206 | snp | C/T | 3.30398e-05 | 0.00406434 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168158 | AGCAGGCTCGTCAGT[C/T]TCAGCTTGCTCAGGA | 10277 |
rs767922732 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071009 | TGCCCTCCACCTCCC[A/G]AGTTCAAGTGATTCT | 10277 |
rs767949573 | snp | A/G | 0.000184087 | 0.00959215 | intron-variant | UBE4B | GRCh38.p7 | 1:10121943 | TTCATCACCGTCCCT[A/G]ATGTTCATGGGTCCA | 10277 |
rs767962451 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144458 | AAGAAAAATATGGCC[C/T]GACGCAGTGGCTCAT | 10277 |
rs767974451 | snp | A/T | 1.64863e-05 | 0.00287104 | intron-variant | UBE4B | GRCh38.p7 | 1:10144897 | AATGGGTAAGATGGA[A/T]CCGGCTGTTTTCTTT | 10277 |
rs767981950 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090943 | AGGAGAAAGTCTTAC[A/G]GACATGAAATTTTTA | 10277 |
rs767983298 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176644 | CCCTAATGTCAAATA[A/C]CATTGGACACCTTTT | 10277 |
rs767983901 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076087 | ATATGATAGCTGTCC[A/G]TTAAAGAGTTTAAAA | 10277 |
rs767986850 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066873 | ATCACGCTACCGCAC[C/T]CCAACCTGGGTGACA | 10277 |
rs768003605 | snp | C/T | 1.65002e-05 | 0.00287225 | intron-variant | UBE4B | GRCh38.p7 | 1:10129346 | GCTACAAATGACAGT[C/T]AGTTTAAGATGAAAT | 10277 |
rs768033622 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041958 | CCTCAGCCTCCCAAA[G/T]TTGTGGGATTACAGG | 10277 |
rs768052659 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146863 | TCTAGAAGCTCTGGA[A/T]CCCAAATTTCCCATC | 10277 |
rs768069488 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163662 | GACAGAGTGAGACTC[C/T]GTCTCAAATAAATAA | 10277 |
rs768077086 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098248 | TAGGAATGCAAGGAT[G/T]CATTGATATTAGAAA | 10277 |
rs768096263 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089295 | CAGGCATGAGCCACC[A/G]TGCTCAGCCAAGAAC | 10277 |
rs768103529 | in-del | -/AAAAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125133 | GTGTCTGGAAAAAAG[-/AAAAAG]AAAAAGAAAAAGAAA | 10277 |
rs768109482 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071632 | GCCATGTCAGCCAAG[G/T]AGGTGTGATAAACAG | 10277 |
rs768123098 | snp | C/T | 1.7141e-05 | 0.0029275 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033640 | ACAGAAGGATCTCTC[C/T]TTAACGCCTTTCACC | 10277 |
rs768147222 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116552 | TCGTAATTAATCCGT[A/G]TGTGTCTTTTATGTA | 10277 |
rs768179939 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146443 | GGCAACAGAGCAAGA[-/CT]CTGTCTCAAAATAAA | 10277 |
rs768200182 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117173 | GTACCTGTGATGTCC[C/T]TTCCAATGCTTAACA | 10277 |
rs768206493 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104184 | CGGTGGAATTGGTCT[A/G]TTTGGTTAAATTGCT | 10277 |
rs768219329 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | UBE4B | GRCh38.p7 | 1:10129471 | CTCACCTGATGGGCT[C/T]GCACATTTTCAGTGA | 10277 |
rs768246347 | snp | G/T | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161268 | GAAGAACAAAGAACA[G/T]TGGGACCAGTTGCCC | 10277 |
rs768255085 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168967 | TATTAAGTAGAATAA[C/T]TGAGACCGTGTAAAA | 10277 |
rs768271058 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048784 | AATGGGAGGAGAGGG[G/T]AGGGAGCTCAGGAGT | 10277 |
rs768286193 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050058 | TATGGGATATTGGTA[G/T]CTGCTTGCTGATCTG | 10277 |
rs768293116 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128838 | CTAAAAAGTGTTTTT[C/T]ATCGTTCTCTAATGT | 10277 |
rs768310047 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139546 | AGTTTTCTGTGTGGG[C/G]ATGTTTTTAATTATG | 10277 |
rs768313472 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143822 | CAAGGAAGCTGCTTC[A/G]GAGGTCAGCCTGACA | 10277 |
rs768326583 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109978 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGTC | 10277 |
rs768337112 | snp | G/T | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095534 | TAATAGCCTTGAAAC[G/T]CAATCTCAGTCTCTC | 10277 |
rs768342451 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070204 | GCATGAACCTGGGAG[C/G]GGGAGGTTGCAGTGA | 10277 |
rs768346797 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146431 | CACTTCAGCCTGGGC[A/C]ACAGAGCAAGACTCT | 10277 |
rs768357514 | in-del | -/TAAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171892 | CTCAAAATAAATAAA[-/TAAG]TAAGTAAGTAAGTAA | 10277 |
rs768379767 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064109 | TACCAACTACTCAGC[A/G]TTCCCTAAACAGTGT | 10277 |
rs768388421 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant | UBE4B | GRCh38.p7 | 1:10130858 | AGTATCAAAGATGAG[C/T]TCCAGATACAGAGCT | 10277 |
rs768390480 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043171 | TGCACCACCATGCCC[A/G]GCTAATTTTGTATTC | 10277 |
rs768400495 | snp | A/T | 1.65952e-05 | 0.00288051 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117559 | AACTACCTCATCGAG[A/T]GTTTCGACCGAGTTG | 10277 |
rs768414284 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121540 | CCAGGACTCCAGGCA[C/T]ACACCATCTTGCCCA | 10277 |
rs768423677 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086067 | AGCTCCACCTCCCTG[A/G]TTCACGCCATTCTCC | 10277 |
rs768438112 | snp | C/T | 1.66156e-05 | 0.00288228 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179895 | TTTTTCTTTTCTCAG[C/T]GCCAGAACTGAAAGA | 10277 |
rs768443411 | snp | C/T | 4.96175e-05 | 0.00498059 | intron-variant | UBE4B | GRCh38.p7 | 1:10119485 | TTGTTTGTTTCTTGT[C/T]GTCCTCACTTCCACC | 10277 |
rs768480265 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041045 | TTTCTTAAGCCTGGG[A/G]GGACAGTGGGATGTA | 10277 |
rs768501522 | in-del | -/GGTAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086471 | TGTAGAGATAAATGA[-/GGTAT]GGGGGGACTCAAAAT | 10277 |
rs768503602 | snp | A/G | 1.65499e-05 | 0.00287657 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103067 | TTCTTCTCTTTCTGC[A/G]CAGTTTAAGCAGAAC | 10277 |
rs768505532 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078096 | CTCACTGCAACCTCC[A/G]TCACCCGGGTTCAAG | 10277 |
rs768545317 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117027 | TTTTGAGATCCATGG[A/T]AGAAGTCACAAAGAT | 10277 |
rs768547702 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152860 | AAGTAGCCATCTTCT[A/G]TCCCTCAGTCTGGGG | 10277 |
rs768558230 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076919 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTATAGA | 10277 |
rs768604873 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165201 | CTTGATGTTGTCCAC[-/A]TCTCCTGCCTGAGTC | 10277 |
rs768608385 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100290 | CATCGTGCCTGGCCT[A/G]TTTTCTCAATTAAAT | 10277 |
rs768633616 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161228 | TGGAGTCTCTGAAGC[A/G]AATCCATGAAGTGCA | 10277 |
rs768678091 | snp | A/C | 1.70269e-05 | 0.00291773 | intron-variant, downstream-variant-500B, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171118 | AGCATGAATTGTCCT[A/C]TTATCCTGTGATTTC | 10277 |
rs768684469 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137131 | CTTTCTCACCCTGCA[C/T]GCTCACCACCTCTCT | 10277 |
rs768688471 | snp | C/T | 1.68272e-05 | 0.00290057 | intron-variant | UBE4B | GRCh38.p7 | 1:10168088 | GGCGCTTTGCTGAGC[C/T]GATGACCAGGACCGA | 10277 |
rs768692055 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112703 | AAATTTATGCATGTA[C/G]TATATTCCGCTTTCT | 10277 |
rs768716008 | snp | A/G | 3.32458e-05 | 0.00407698 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168240 | GTTCCACATCCTCAC[A/G]AAGCAGGTCCAGAAG | 10277 |
rs768755354 | snp | C/T | 1.69407e-05 | 0.00291034 | intron-variant | UBE4B | GRCh38.p7 | 1:10072016 | GAATGCCCTTTTCCC[C/T]TCATGTTGTAGATTC | 10277 |
rs768755967 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165764 | TCAGGGATACCTTCC[C/T]TGACCACCCTTTCCA | 10277 |
rs768757522 | snp | C/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032021 | GCCTCCCGAGTAGCC[C/G]GGACTACAGGCGCCC | 10277 |
rs768763500 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113785 | CATAAGATGCTTTTC[A/G]GCCGGACGCAGTGGC | 10277 |
rs768764486 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166940 | AAAAAAAATAAATAA[-/AT]CACACACACACACAC | 10277 |
rs768783317 | snp | A/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144999 | CCCCACTGGCAACTA[A/G]ACACCGCGAAATGCT | 10277 |
rs768796982 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068924 | TCCAGCGGATCTTTA[A/G]GATGGGGCAAAATGT | 10277 |
rs768816973 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160826 | TGTGTGCCTGTAGTT[-/C]CAGCTACTTAGGAGG | 10277 |
rs768817664 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10121992 | GTCCTTCCTAGTGCC[A/G]TATATGCTGTGTAGG | 10277 |
rs768836201 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103673 | GTCTTGCTCTGGCAC[C/T]AGGCTGGAGTGCAGT | 10277 |
rs768836336 | snp | G/T | 1.65748e-05 | 0.00287874 | intron-variant | UBE4B | GRCh38.p7 | 1:10146930 | ACTTAGCTACTGACT[G/T]ATCTTTGGGTGGGGA | 10277 |
rs768862044 | snp | A/G | 1.80117e-05 | 0.00300092 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106556 | GTGCCACGAGCAGAC[A/G]CCCCTCCTCCCTGAG | 10277 |
rs768865181 | snp | A/C | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032576 | CCAGTGGGAGCGATG[A/C]GGTGTTTCTAGGCCC | 10277 |
rs768868657 | snp | A/G | 1.73987e-05 | 0.00294942 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106202 | ACTAATTTAGCCTCT[A/G]TGAAAGTAGTCCGGC | 10277 |
rs768888948 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058339 | TGACCGTGCCATTCT[A/G]CCCCCGTCTGTTTCC | 10277 |
rs768918175 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033833 | CCAAGAATAACGTGA[A/C]TCCCCGATAGGGTCT | 10277 |
rs768929144 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169367 | TGTGACTCTCTGTTA[C/T]GTGACTCCTGTCATC | 10277 |
rs768929935 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125456 | TCTCTTCCAGAGCTG[C/T]ATTGATATCTCACAA | 10277 |
rs768966151 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094845 | ACCTAGGCTGGAGTG[C/T]GGTGGTGTGATCTTG | 10277 |
rs768968395 | snp | A/C | 1.80279e-05 | 0.00300227 | intron-variant | UBE4B | GRCh38.p7 | 1:10132530 | GTCAAATTCATTCAT[A/C]TGACCCAGATTTAGT | 10277 |
rs768969960 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072128 | CTCCGGGGCCTCCCA[C/T]AGCGGCATCAGCCCC | 10277 |
rs768978794 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065665 | GTCTTGGAGTGAAGA[C/T]GTTATGGAGCAGGGC | 10277 |
rs768995228 | snp | C/T | 1.65836e-05 | 0.0028795 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106275 | GTCTCTTGCCTCACC[C/T]TCCCGTGCAGCCAGC | 10277 |
rs769002464 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076603 | GGTAAAAAGTCCTTC[A/T]TCCAGGAGTGCTTGG | 10277 |
rs769022467 | snp | G/T | 1.64871e-05 | 0.00287111 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101076 | GCGGATTTATAAAAG[G/T]TAAAAGGCTTGTTTG | 10277 |
rs769030131 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067438 | AAAAAAGGACTTTTG[C/T]TTAACTTAAAGGAGA | 10277 |
rs769112870 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033783 | CCAGTGCTGTCTGGC[C/T]TTTGGGCTTGGAGAA | 10277 |
rs769116297 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106114 | GATTCTCCTTTAAAA[A/G]CTTGATATTTTCTGT | 10277 |
rs769135419 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151542 | GTTGTTGGTACCTTC[C/T]CTGATGAAGTTTTAT | 10277 |
rs769164247 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147796 | TTGATCACTTTGTCA[A/T]CAACTGGTCATCTCC | 10277 |
rs769172021 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072944 | ATAATTTGATAGCCT[C/T]CTGAATCATCTGTCT | 10277 |
rs769176794 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118130 | GGCTGGGCTTAAACT[C/T]AGTAAGCTACCCTTT | 10277 |
rs769184373 | in-del | -/G | 1.65217e-05 | 0.00287412 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095429 | AACATTATTTCACAT[-/G]GGGCTTCATCCTTCC | 10277 |
rs769223036 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093756 | CTGCAGGGCAGTGGG[A/G]CGATCTTGGCTCACT | 10277 |
rs769225390 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059772 | GGCATCCGAAGTTGT[A/T]GAGCGTATCTGGAGG | 10277 |
rs769225770 | snp | A/G | 0.000364631 | 0.0134975 | intron-variant | UBE4B | GRCh38.p7 | 1:10107410 | TACCCCTGCATGTGC[A/G]TAGATGCTTAGGAAC | 10277 |
rs769233961 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039066 | CTCCATCAAAAAAAC[-/A]AACAAACAAAAAAAC | 10277 |
rs769262110 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147610 | TAGGCAAATGTCAAC[A/G]CCTGTTATTTTAATT | 10277 |
rs769265204 | snp | A/G | 1.66835e-05 | 0.00288816 | intron-variant | UBE4B | GRCh38.p7 | 1:10119655 | ATTAGCAGGCAGAGA[A/G]CCCTAGCCGTCAGTG | 10277 |
rs769331364 | snp | C/G | | | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106447 | AGCTCCCCAAGTCCC[C/G]CTGCCCTCGCCAGTA | 10277 |
rs769362294 | in-del | -/T | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151488 | CCACGAACCCAGAAG[-/T]TTTTTTGAAATGATT | 10277 |
rs769367309 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060063 | CAGTCCTGTTCTATT[C/G]AGTCGTCAGGTCCCT | 10277 |
rs769405511 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091555 | GCTCAAGCAATCCTT[-/C]CACCTCACCCTCTCA | 10277 |
rs769408752 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148828 | GCCTGTAATCTCAGC[C/T]ATTCGGGAGGCTGAG | 10277 |
rs769423461 | in-del | -/A | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031538 | GGCAATAATGAGGTT[-/A]AAAAAAGTAAACTTT | 10277 |
rs769459301 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102636 | GGCTGGTCTTGAGCT[C/T]CTGACCTCAGGTGAT | 10277 |
rs769460298 | snp | C/T | | | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117552 | TATGCTGAACTACCT[C/T]ATCGAGTGTTTCGAC | 10277 |
rs769464315 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086935 | TCTCGGCCTCCCAAA[C/G]TGCTGGGATTATAGG | 10277 |
rs769468317 | snp | A/T | 1.65135e-05 | 0.00287341 | intron-variant | UBE4B | GRCh38.p7 | 1:10126904 | TTCTTTTTCTTTAAC[A/T]CATTCAATAGATGTT | 10277 |
rs769472164 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040767 | GGATTACAAGCATGT[A/G]CCACCATGCCTGGCT | 10277 |
rs769495414 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119669 | AGCCCTAGCCGTCAG[G/T]GGACATCAGGCTCTC | 10277 |
rs769507214 | snp | C/T | 3.71657e-05 | 0.00431063 | intron-variant | UBE4B | GRCh38.p7 | 1:10178605 | CTTTTTTCCACCTGA[C/T]GTACATTTACGTCTC | 10277 |
rs769512745 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173711 | CCAGGGCTCTTCCAT[C/T]GTTGCCGTAGAGAGA | 10277 |
rs769533285 | snp | A/G | 3.29457e-05 | 0.00405854 | intron-variant | UBE4B | GRCh38.p7 | 1:10130629 | GATGTAAGTATAGTG[A/G]CTACTTGTACTTTGC | 10277 |
rs769545074 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071699 | TTATGTATGTATTTA[C/T]GTATGTATGAATTAG | 10277 |
rs769581689 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125164 | AGATTATGCTTAGTA[-/AT]ATATTTTACCTGTGC | 10277 |
rs769600050 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079717 | AACTAGTGAGAAGCC[A/G]GATGATATATTTGGC | 10277 |
rs769606639 | snp | C/T | 3.31186e-05 | 0.00406918 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117537 | CTGCAAAGAGACAGA[C/T]ATGCTGAACTACCTC | 10277 |
rs769630874 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10099099 | CAAAAAAAATTAGCC[A/G]GGCATGGTGGTGCGT | 10277 |
rs769638109 | snp | C/T | 0.000185237 | 0.00962206 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107355 | GGTGATGATTTTTCT[C/T]GTGTCCAGTTTGGGT | 10277 |
rs769648244 | in-del | -/ATTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124158 | AGACCTGTTTATTCT[-/ATTA]ATTAATTAATTAATT | 10277 |
rs769678111 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153859 | AGGCTGAGGTGGGCG[A/G]ATCACCTGAGGTCGG | 10277 |
rs769736965 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130232 | GGCGCACACCACCAC[A/G]CCCGGCTAATTTTTG | 10277 |
rs769742240 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050331 | CCTGCCTTGGCCTCC[C/T]AAAGTGTTGGGATTA | 10277 |
rs769753354 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064228 | TCAAGTAGTAAGCAC[A/G]TAGCATTTGTATGTG | 10277 |
rs769753754 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | UBE4B | GRCh38.p7 | 1:10102934 | ATTAACCTGCAAATC[C/T]TCTTCTTCACCAGGA | 10277 |
rs769761041 | snp | C/G | 1.65633e-05 | 0.00287774 | intron-variant | UBE4B | GRCh38.p7 | 1:10179578 | GTAGAGGAGGGTGCA[C/G]TTTGAGGTGCAGCGC | 10277 |
rs769772506 | snp | G/T | 1.65526e-05 | 0.00287681 | intron-variant | UBE4B | GRCh38.p7 | 1:10119633 | GAAGACCCGTGACGT[G/T]CTTGACATTAGCAGG | 10277 |
rs769832402 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144844 | TACAATGCGAAAACA[A/G]ACAACTGCGTGTGAG | 10277 |
rs769839019 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059866 | GGGGCATAGGTCTTC[A/G]GCCCAAGCCAAGGGA | 10277 |
rs769849738 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178114 | CATGTGCTAGTGCTG[A/C]ACTAAATGAGCTTGA | 10277 |
rs769884068 | snp | C/T | 1.66638e-05 | 0.00288645 | intron-variant | UBE4B | GRCh38.p7 | 1:10179878 | GGGCATTAATCCTCC[C/T]TTTTTTCTTTTCTCA | 10277 |
rs769935464 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120474 | GTTGCAGCCGAGATC[A/G]TGCCACTGCACTCCA | 10277 |
rs769944570 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055656 | CAGGCGCAGTGGCTC[A/G]TGCCTGTAATCCCAG | 10277 |
rs769947436 | snp | A/G | 8.89529e-05 | 0.00666847 | intron-variant | UBE4B | GRCh38.p7 | 1:10132524 | CTGTTTGTCAAATTC[A/G]TTCATCTGACCCAGA | 10277 |
rs769971141 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176141 | TTCACTTAGCATCAT[G/T]TTTCAAGGTTCATTT | 10277 |
rs769973260 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056988 | TGGCTCATTTTTGTA[-/T]TTTTTTTTTTTCTGT | 10277 |
rs769978598 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090379 | CTCCACCTTGGCCTC[C/T]AAAAGTTCTGGAATT | 10277 |
rs769978826 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111197 | AGGCCCTGCATCTCA[C/T]GTACACTCCACATAC | 10277 |
rs769997867 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170897 | GGCTTCTTTTGGTAT[C/T]TATAAATAAATATTT | 10277 |
rs770018903 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164888 | GGTATAATAATAACT[C/G]ATGATGAGAAACCAT | 10277 |
rs770063679 | snp | A/T | 1.68969e-05 | 0.00290657 | intron-variant | UBE4B | GRCh38.p7 | 1:10072262 | GTAATTCTTCTTAGC[A/T]TTTTGTTAAGCTGAT | 10277 |
rs770085665 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083449 | CATCTGTAGGAATGT[A/C]AACAAGATCAAAGCC | 10277 |
rs770092676 | snp | C/T | 5.30931e-05 | 0.00515206 | intron-variant | UBE4B | GRCh38.p7 | 1:10106193 | CCTTTCTCAACTAAT[C/T]TAGCCTCTATGAAAG | 10277 |
rs770101854 | snp | C/T | 3.32016e-05 | 0.00407427 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106396 | CCCTACACTGTCACT[C/T]ACCCATGGGCGTCCT | 10277 |
rs770135711 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10033996 | ATGCGAACAAGAAGG[A/G]CGAGATTTACATGAA | 10277 |
rs770145784 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155843 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 10277 |
rs770159407 | snp | C/T | 1.67598e-05 | 0.00289476 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106481 | CCCAAGCAGTGCCCG[C/T]CAGCAGTTCCAGACA | 10277 |
rs770192497 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046264 | ATGTGTTCAGCTATA[C/T]GTTCTCTCACATCAG | 10277 |
rs770245877 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032821 | TCCCCACGTCCGGCG[C/T]GGCTGCGCGGGACGG | 10277 |
rs770248292 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067686 | TTATGGCTCTCTGCA[A/G]CCTTGACCTTCCCAG | 10277 |
rs770277863 | snp | A/C | 4.94254e-05 | 0.00497094 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095489 | AAGCCAGAGCAGTGA[A/C]GGAGTCAGTTCTCTC | 10277 |
rs770280729 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137707 | TTCATTAGCACCATG[G/T]TTGTGTTTCTTACTC | 10277 |
rs770285333 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152129 | AAATTAGCCGGGCAT[A/G]GTTGCAGGTGCCTGT | 10277 |
rs770313149 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071577 | TGGGTGACAGAGAGA[-/CT]CTCTCTAAAATGAAG | 10277 |
rs770333743 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109080 | AGGAATAAAATGTAC[C/T]AAGTGTATAAAAATA | 10277 |
rs770338844 | snp | C/T | 6.60142e-05 | 0.0057448 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149228 | CCAAGGTATTTGCAG[C/T]GTTGCCTGAGTTTTA | 10277 |
rs770362236 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148906 | GATTGCACCACTGCA[C/T]TCCAGCCTGGGTGAC | 10277 |
rs770365004 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124418 | GTCTTGAACTCTTGG[A/C]CTCAAGTGGTCCGCC | 10277 |
rs770377942 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137313 | TGGGGGAGGTATGTA[C/T]GTTATATAGTGTTCT | 10277 |
rs770394080 | snp | C/T | 1.68292e-05 | 0.00290075 | intron-variant | UBE4B | GRCh38.p7 | 1:10151308 | GGTCTCTTTCTTGCT[C/T]TTCTTGCCTCTGTTC | 10277 |
rs770396000 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127311 | GTGCAGAAAATCTCA[A/G]TGTAGCTCTCTTGTT | 10277 |
rs770397872 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061526 | AAAGTGCTGGTATTA[C/T]AGGGGTGAGCCACCG | 10277 |
rs770399707 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169634 | AAGGCCAGATAGTAA[A/G]TAGTTGATTAATTCC | 10277 |
rs770405723 | snp | C/T | 1.65225e-05 | 0.00287419 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179542 | ACCGGCAGACGCTGA[C/T]AGAGAGCATGCTGGA | 10277 |
rs770497980 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047039 | TCTAAGATATCACGG[G/T]TTTTGCCAAATGTTT | 10277 |
rs770512320 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046567 | GCGCTTCCTCCCCTG[A/G]CAGTACTGTGAGGTT | 10277 |
rs770528927 | snp | C/T | 0.000105169 | 0.00725076 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10107239 | TGTACGACAATCCTT[C/T]CTCCTTCCTCTTCCT | 10277 |
rs770532269 | snp | G/T | 1.65392e-05 | 0.00287564 | intron-variant | UBE4B | GRCh38.p7 | 1:10158491 | AGTTCAAGTGAGTAT[G/T]GGGCCCCTCGTGTCA | 10277 |
rs770541476 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117623 | GAAATGGATTAACTT[-/AA]AAAAAAAAAAGCCTA | 10277 |
rs770547824 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091989 | CCTGGCCTCAAGTGA[C/T]CCTCTCTCCTTGACT | 10277 |
rs770572570 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041025 | TCACTTTATAACCAG[A/G]ACTCTTTCTTAAGCC | 10277 |
rs770572719 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161477 | ATCTGAAGCTAAGAA[A/G]TGGGTTGAGAAGTCT | 10277 |
rs770577334 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107737 | CACCCGCCACCATGC[C/T]CGGCTAATTTTTGTA | 10277 |
rs770598489 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076246 | GCTTCTTTCTTTCTT[G/T]CTTTTTTTTTTTTTT | 10277 |
rs770599640 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075350 | GTTTCTTCTCATCAC[C/T]TCCACCGCTATTACC | 10277 |
rs770602208 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044036 | ACAATTCCACGTTTC[G/T]TTTCTTTTCTTTTTT | 10277 |
rs770628498 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095133 | TTTTTCTGGACTATC[A/G]TGGAAGTTAATTTGT | 10277 |
rs770698545 | snp | C/T | 0.000922828 | 0.0214607 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103029 | GTCTCTTGGAAGGAC[C/T]GGGACAGAGATGTCA | 10277 |
rs770713686 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050054 | CAAATATGGGATATT[-/G]GTAGCTGCTTGCTGA | 10277 |
rs770731606 | snp | C/T | 5.2415e-05 | 0.00511906 | intron-variant | UBE4B | GRCh38.p7 | 1:10071977 | CATTCTCTGGCAGAA[C/T]TGTGTTTCTGCTGAT | 10277 |
rs770766707 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034954 | AGTTTCTTTCATTCG[C/G]TAGGAAATCTCCTTA | 10277 |
rs770787455 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086991 | CGTCTCTTTTTTAGT[A/G]CTTAGGTATGCTAAA | 10277 |
rs770789712 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162882 | CTTTTCTTCTTATGT[A/G]TTAAAGTTCTACCCA | 10277 |
rs770793491 | snp | C/G | 1.66799e-05 | 0.00288785 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179433 | CCTCTGATGGACACC[C/G]TCATGACAGACCCCG | 10277 |
rs770803856 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053491 | GATGGAATTTTGCTC[A/G]TCGCCCAGGCTGGAG | 10277 |
rs770838519 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174853 | TTGGTGGGGCAGGGG[A/G]CGGTAAGTGCAGAAG | 10277 |
rs770847448 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131171 | TTAATATGTCTTCAA[C/T]TCTCAAACTTAAAGG | 10277 |
rs770848444 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113878 | GAGATCATCCTGGCC[A/G]ACATGGTGAAACCCC | 10277 |
rs770870412 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100773 | TGGTCAGGCTGATCT[C/T]GAACTCCTGACCTCA | 10277 |
rs770877861 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052465 | TTCTAAGATGTCCGG[A/G]TAGATCATATTGAGC | 10277 |
rs770894170 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065807 | TTTACTGTGTCATTG[C/T]CATTTGCATTTATGT | 10277 |
rs770898862 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118291 | TTGGGCTTTGTTGTA[C/T]TTAGCCTTAGTGGAA | 10277 |
rs770919627 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094436 | GATTCTATCATTAAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs770966208 | snp | A/G | 1.86333e-05 | 0.00305226 | intron-variant | UBE4B | GRCh38.p7 | 1:10106590 | CTCTCCTAGGTATTT[A/G]TCCCACAGGAGAGTT | 10277 |
rs770984248 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044437 | CCAGGGACTGGTTTC[A/G]TAGAAGACACTTTTT | 10277 |
rs770985971 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130765 | CATTACCCTGGAAAA[C/T]ACTCGTGTGGTTAGC | 10277 |
rs771001830 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133975 | GGATCACTTAAGCCC[A/G]GGAGGTTGAGGCTGC | 10277 |
rs771022422 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154559 | ATAAAAACAACTGGC[C/T]GGGCTCAGTGACTCA | 10277 |
rs771034338 | snp | C/T | 4.96479e-05 | 0.00498212 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179922 | AAGAGCAGATTCAGG[C/T]GTGGATGAGAGAGAA | 10277 |
rs771047553 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152993 | GCTGGTGTCTCTCTC[C/G]GGGGTTGTGCACGGT | 10277 |
rs771076432 | snp | C/G | 3.30038e-05 | 0.00406212 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149214 | AAATTCAGATGTCCC[C/G]AAGGTATTTGCAGCG | 10277 |
rs771093729 | snp | C/G/T | 0.000181548 | 0.00952592 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161277 | AGAACAGTGGGACCA[C/G/T]TTGCCCCGGGTGAGG | 10277 |
rs771105509 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176307 | AGTGCTGCTATGAAC[A/C]TTTGTGTAAAAGTAT | 10277 |
rs771121903 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178430 | CACATATTATTCCAG[A/T]CTTTATCCATTTGTA | 10277 |
rs771158504 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142913 | AGGAGTTTGAGACCC[A/G]CCTGGCCAACATGGT | 10277 |
rs771193816 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175513 | AAAATTAGCCAGGCG[G/T]GGTGGCGGGCGCCCG | 10277 |
rs771211939 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179408 | TTTGCTTTGCTTTGT[A/C]CCCGCAGACCCTCTG | 10277 |
rs771232918 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145164 | TTCTTTTCCCTTCCA[A/G]TAAAATAGTATATTT | 10277 |
rs771241076 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116308 | CCACCACGCCCAACA[A/G]ATTTTTGTATTTTTA | 10277 |
rs771285604 | snp | C/T | 1.65075e-05 | 0.00287289 | intron-variant | UBE4B | GRCh38.p7 | 1:10126899 | CTTTGTTCTTTTTCT[C/T]TAACTCATTCAATAG | 10277 |
rs771315211 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115659 | ACATGTGTCCTTTAA[C/T]GAGAGGGATACATTC | 10277 |
rs771333173 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072151 | TCAGCCCCAGGACCC[C/T]CTCAGAGTCTTGGTC | 10277 |
rs771367268 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148631 | GGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 10277 |
rs771381248 | in-del | -/C | 1.66103e-05 | 0.00288182 | frameshift-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171147 | TCCTAGGAGCTTGGA[-/C]CCCGATTGGCTGCAA | 10277 |
rs771390590 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055731 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 10277 |
rs771407650 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158505 | TGGGGCCCCTCGTGT[A/C]ACAACTTGCTTTCTT | 10277 |
rs771436809 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069293 | CAGTGCATTTTTCTA[A/G]TATTTCTCATTTATT | 10277 |
rs771447743 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140934 | GTCACTGTCAATTCA[A/G]AGTTTGGGTCAACTA | 10277 |
rs771462683 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102496 | GTTCACCACAACCTC[C/T]GCCTCCTGGGTTCAA | 10277 |
rs771469061 | snp | G/T | 1.66225e-05 | 0.00288287 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171365 | TCTCTGTGAGTTTAC[G/T]GGCAGATTTGGAGAT | 10277 |
rs771496523 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123937 | TGCCACCACACCCAG[A/C]TAATTTTTTGTATTT | 10277 |
rs771511584 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant | UBE4B | GRCh38.p7 | 1:10072233 | AGCCCAAGCTTCATA[C/T]CTGGGACTCTTTTGT | 10277 |
rs771531954 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130910 | TGCCCAGTAGACAAA[C/T]GGCTAACAAAAGCCA | 10277 |
rs771549756 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084498 | GCCACACAAACCACT[C/G]TTAGTTTTGGGTGCA | 10277 |
rs771550549 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048508 | CATCCATTCCAGCAA[A/T]TAAAGGTTGGGAGAT | 10277 |
rs771630942 | snp | A/C/T | 4.9464e-05 | 0.00497292 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151378 | GATATTGTGATGTTC[A/C/T]TTGTTGTGATGTTGT | 10277 |
rs771632753 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157646 | AGCAGGGCGTGGTGG[C/T]GCATGTCTATAGTCC | 10277 |
rs771640318 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172871 | TCATATTATAATACC[A/G]TATTTTCACTGTACC | 10277 |
rs771664464 | snp | A/G | 8.3423e-05 | 0.00645791 | intron-variant | UBE4B | GRCh38.p7 | 1:10102903 | TGAAACACCTAACTC[A/G]TACCTCTTATTTGAA | 10277 |
rs771715272 | in-del | -/TTC | 1.67122e-05 | 0.00289064 | intron-variant | UBE4B | GRCh38.p7 | 1:10072251 | GGGACTCTTTTGTAA[-/TTC]TTCTTAGCTTTTTGT | 10277 |
rs771715786 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164353 | CTCCGTCTCAAAAAA[-/C]GAAAAAAAAAAAGAA | 10277 |
rs771720345 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154022 | GCGAGGCAGAGGTTA[C/T]GGTGAGCCAAGATCG | 10277 |
rs771736573 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158703 | AGATACTTTGGGGGT[A/G]GTACACAAGCGAAGA | 10277 |
rs771746053 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149666 | TAAAATTGGAGAATG[C/G]TTACCAAGAAATGGT | 10277 |
rs771758290 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120350 | ACATGGCAAAATTCC[A/G]TCTCTACTAAAAATA | 10277 |
rs771778571 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166495 | CTCATAGTTTTAAAA[C/T]AATGAAGACTGGCTG | 10277 |
rs771789329 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048683 | AGAGGAGGACCAAGA[C/T]GTGACTATGGGATTT | 10277 |
rs771796720 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069592 | CAGGCTGGAGTGCAG[C/T]GGTGCGATATTGGCT | 10277 |
rs771810611 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096396 | GGCTCCTCTCCCCTC[A/G]AGCAGTGGCCTCGGT | 10277 |
rs771817115 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | UBE4B | GRCh38.p7 | 1:10105493 | CTGTGTGTAACCTGT[C/T]CTTTGTTCTGCCTTT | 10277 |
rs771820243 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171465 | GAAGAGCAGATTTGG[G/T]CTGGGCGCGGTGGCT | 10277 |
rs771834718 | snp | C/G | 3.78896e-05 | 0.00435239 | intron-variant | UBE4B | GRCh38.p7 | 1:10106633 | GCGGTGCAGGGAAAG[C/G]AGATTAACACGGTTT | 10277 |
rs771839700 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130024 | TATTCGAGTCCTTTG[-/GT]GTGGTATAAGAAGAG | 10277 |
rs771856770 | snp | C/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119606 | CAAGGCTCCCTAACA[C/G]AGCCCAGGTATGAAG | 10277 |
rs771868798 | snp | G/T | 1.994e-05 | 0.00315747 | intron-variant | UBE4B | GRCh38.p7 | 1:10144932 | TGACTGTTAGTCTTT[G/T]ATTTCAGAACTGTAG | 10277 |
rs771871986 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105644 | ATTGCTGCAGCAGCA[C/T]GGTCACCAGACAGAA | 10277 |
rs771887634 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101978 | CTCTGCATTTAGGGT[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs771911074 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076892 | GCTGGGATTACAGGC[A/G]CCTGCCACCACGCCT | 10277 |
rs771939110 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164630 | ATTGATTTTTCCTGT[A/G]TTAATGGATGAAAAA | 10277 |
rs771944250 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042234 | CGGCACTTGTAGTAT[C/T]TAGTGGAAATGTCTT | 10277 |
rs771956996 | snp | C/G | 1.64852e-05 | 0.00287094 | intron-variant | UBE4B | GRCh38.p7 | 1:10137228 | CCATGATACCGTGTC[C/G]TGGGATTGCCTGAGT | 10277 |
rs771979239 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087666 | CCATCACATCGTATC[-/A]GGGGTATATAATATC | 10277 |
rs771994633 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040691 | GGCGCGATCTCAGCT[C/T]GCTGCAACCTCTGCC | 10277 |
rs772003173 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075455 | TGCTTCACTTGAGTC[A/T]GTTCTCAGTGTAGAG | 10277 |
rs772034759 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041484 | TGATTACAGGCTCCC[A/G]CCAGCATGCCCAGCT | 10277 |
rs772043513 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109214 | GGGGAACGGGGGGGC[C/T]GGGGGGACAGACAAG | 10277 |
rs772120098 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123001 | CCAAGAATAAAAATT[C/T]CAGTTAGTGTTGTGT | 10277 |
rs772123342 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055460 | GCTAGGACTACAGGC[A/G]TGTGCTGCCACACCC | 10277 |
rs772136828 | snp | C/T | 1.65296e-05 | 0.00287481 | intron-variant | UBE4B | GRCh38.p7 | 1:10146949 | TTTGGGTGGGGACAT[C/T]CCTGCTTCCACAGAA | 10277 |
rs772140471 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085119 | GAGTTGAACGTTCAT[-/A]ACCTGGAGAGCCTTA | 10277 |
rs772144230 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176558 | TTAAACATGTTAATT[G/T]GTTTTTGTTTCTTAA | 10277 |
rs772153110 | snp | A/G/T | 0.000116059 | 0.00761691 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106280 | TTGCCTCACCTTCCC[A/G/T]TGCAGCCAGCCAGTT | 10277 |
rs772171808 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154038 | GGTGAGCCAAGATCG[C/T]GCCATTGTAATCCAG | 10277 |
rs772175245 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058133 | GCTGTAGCGGAGTGC[A/T]TGGGTAAAAGCACTA | 10277 |
rs772186082 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124199 | GTGAGTCTCTCTCTG[A/T]TACCCAGGCTGGAGT | 10277 |
rs772209228 | snp | A/C | 0.001056 | 0.022954 | intron-variant | UBE4B | GRCh38.p7 | 1:10130633 | TAAGTATAGTGGCTA[A/C]TTGTACTTTGCTGCC | 10277 |
rs772260738 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130743 | AAAAATACTTCTCAG[G/T]GCCTGCCATTACCCT | 10277 |
rs772265161 | snp | C/T | 8.26959e-05 | 0.0064297 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135080 | CAAGTTAGAAACAGT[C/T]GATCCCACGTATATT | 10277 |
rs772292646 | snp | A/C | 3.29495e-05 | 0.00405877 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072143 | TAGCGGCATCAGCCC[A/C]AGGACCCTCTCAGAG | 10277 |
rs772318540 | in-del | -/AAAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136921 | GCAAAAGTCCATCTC[-/AAAT]AAATAAATAAATAAA | 10277 |
rs772340316 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156490 | AGTGATCTGCCCACC[C/T]GGGCCTCCTGAAGTG | 10277 |
rs772364898 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058478 | ATGTGTTAAAACTTG[C/T]GCTGGAGAAAGTGCA | 10277 |
rs772365347 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10105932 | ATTTTTTGGCTCTCT[A/G]TGGTTAAGATATTGC | 10277 |
rs772381420 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031238 | GGGATTACAGGTGCC[C/T]GCCACCACGCCCTTC | 10277 |
rs772384198 | snp | C/T | 3.34672e-05 | 0.00409054 | intron-variant | UBE4B | GRCh38.p7 | 1:10122084 | TCAAGCAGGTACGGT[C/T]GTATGAGTTTGCTCT | 10277 |
rs772419858 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171925 | AAAAAACAAAAGTAA[A/G]GAGCAGGTTTGGCGC | 10277 |
rs772422586 | snp | A/G | 8.25103e-05 | 0.00642249 | intron-variant | UBE4B | GRCh38.p7 | 1:10072217 | ATAGGTGCATCAGGT[A/G]AGCCCAAGCTTCATA | 10277 |
rs772428551 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079857 | TGTTGACTCAAATGG[C/T]CTTCATCCTGCTTCC | 10277 |
rs772438210 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106841 | TGGGGCACACAGGAA[C/T]CCTTTTTGGCCTTTT | 10277 |
rs772438325 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069886 | CTGTTAAGTGACTTA[C/T]CTGGATAGGCTCCAG | 10277 |
rs772446277 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166539 | ACACTTGTAATCCCA[G/T]CACTTTGGGAGGCCT | 10277 |
rs772471846 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103934 | CCTGGCCTCATTTTT[G/T]TAGTTTTAGTAGAGA | 10277 |
rs772491298 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050561 | AATTATTTATTCACT[C/T]GGTGTAGCTCCTACT | 10277 |
rs772492315 | snp | A/G | 1.97736e-05 | 0.00314427 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135180 | AATGACTGGCTGACT[A/G]AACTCTGTGAGTACT | 10277 |
rs772495937 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137459 | GGTTACTACAGACTT[-/C]CCATTAACTTTTCCC | 10277 |
rs772526841 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091965 | TGTTGCCCAGGCTGG[C/T]CTCAAACTCCTGGCC | 10277 |
rs772612630 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085943 | TACAGGCACCCACCA[C/T]CACGCCCAGCTAATT | 10277 |
rs772626231 | in-del | -/T | 3.40872e-05 | 0.00412825 | intron-variant | UBE4B | GRCh38.p7 | 1:10126778 | ATATTTCTGATTTTG[-/T]TTTTTTTTCTTATAG | 10277 |
rs772633608 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106085 | TTATCTGCTAGATAT[A/G]CTTGAACTGAAATGA | 10277 |
rs772650238 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101147 | AGGAATTGAAAACAT[A/G]GAGGTTGATGAAAAT | 10277 |
rs772667676 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071489 | GATACTTAGGAGGCC[A/G]AGGTGGGAAGATTAC | 10277 |
rs772667961 | snp | G/T | 1.64822e-05 | 0.00287068 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171179 | GCTGAACTTTAATCT[G/T]CAGCAACTTTGTGGC | 10277 |
rs772673506 | in-del | -/C | 3.32135e-05 | 0.004075 | intron-variant | UBE4B | GRCh38.p7 | 1:10161122 | ATGTATGACCATGTA[-/C]AATATAATTGCCTTT | 10277 |
rs772688292 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169849 | GCGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 10277 |
rs772730213 | in-del | -/ACAC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111045 | CTTTCTCTGTCTCTG[-/ACAC]ACACACACACACACA | 10277 |
rs772739826 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095032 | GGTCCACCTGCCTTG[A/G]CCTCCCAAAGTGCTG | 10277 |
rs772755592 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107413 | CCCTGCATGTGCGTA[A/G]ATGCTTAGGAACTAA | 10277 |
rs772756837 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166942 | AAAAAATAAATAAAT[-/CA]CACACACACACACAC | 10277 |
rs772776170 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095574 | CAGAGCATGGATATC[A/G]ATGGTGTCTCATGTG | 10277 |
rs772791151 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120264 | GGTGGCTCACACCTG[A/T]AATCCCAGCACTTTG | 10277 |
rs772803836 | snp | A/G | 1.66776e-05 | 0.00288765 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106456 | AGTCCCCCTGCCCTC[A/G]CCAGTAGCCCCCAAG | 10277 |
rs772815035 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046337 | CGAGGGAGACAACCC[C/T]GGATCAACTTCAGAG | 10277 |
rs772840670 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143230 | CCAACATGTTGAAAC[C/G]CCATCTCTACTAAAA | 10277 |
rs772841228 | snp | C/T | 0.000110571 | 0.00743458 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106577 | CCTCCCTGAGGATCT[C/T]TCCTAGGTATTTATC | 10277 |
rs772854315 | snp | C/T | 3.30972e-05 | 0.00406786 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135085 | TAGAAACAGTTGATC[C/T]CACGTATATTTTTCA | 10277 |
rs772856980 | snp | C/G | 1.64857e-05 | 0.00287099 | intron-variant | UBE4B | GRCh38.p7 | 1:10137230 | ATGATACCGTGTCCT[C/G]GGATTGCCTGAGTTA | 10277 |
rs772874655 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147908 | ATTGGCCCAAGACCC[A/G]TGAAGGCGTGGAAAA | 10277 |
rs772878881 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117660 | TTGTTTGATTATCCC[A/C]ACCCCTGGAGCATTC | 10277 |
rs772881150 | in-del | -/T | 0.219135 | 0.248087 | intron-variant | UBE4B | GRCh38.p7 | 1:10072436 | TCCATAACTTCCATC[-/T]TTTTTTTTTTCAAAC | 10277 |
rs772885179 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148833 | TAATCTCAGCTATTC[A/G]GGAGGCTGAGACATG | 10277 |
rs772892124 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10168344 | CTTATAACTTTAGCA[A/G]TTGTTGAAGTTCTGG | 10277 |
rs772899779 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117465 | TCTCTGAAGTTTGGG[A/G]GCCTCTGGTGGAGCA | 10277 |
rs772915743 | in-del | -/TTTCT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044032 | GACCACAATTCCACG[-/TTTCT]TTTCTTTTCTTTTTT | 10277 |
rs772916878 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090434 | TGAGACCTGTGTTTT[-/A]ACTCTTTGCTCTGTT | 10277 |
rs772918002 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166114 | CACAGACTGGAGCAC[-/T]TTTCCCAGAGGGCAC | 10277 |
rs772928952 | snp | A/G | 0.000296467 | 0.0121715 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105645 | TTGCTGCAGCAGCAC[A/G]GTCACCAGACAGAAA | 10277 |
rs772929413 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058987 | GCGCGGTAGCTTGTG[C/T]CTGTAATCCCAGCAC | 10277 |
rs772931755 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174846 | GAGAGCTTTGGTGGG[G/T]CAGGGGGCGGTAAGT | 10277 |
rs772945603 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10073479 | GTAATCCCAGCACTT[A/T]GGGAAGCCAAGGTGG | 10277 |
rs772960651 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138331 | CTTGATCTCCTGACC[C/T]CGTGATCCGCCCGCC | 10277 |
rs773024345 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116776 | TTTCATTAAAACCCC[A/G]CTGCAAAAGAGATGG | 10277 |
rs773037134 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039117 | AAAAAAGCAATTATA[A/G]TTAAATTTGAGTAGA | 10277 |
rs773041187 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160258 | TCAATATTACAGGTT[C/G]CAATTTTTCTTCCAT | 10277 |
rs773053143 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052263 | TTTTTGTAGAGACAG[A/G]GTCTCACTATGTTGC | 10277 |
rs773071983 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050354 | TGGGATTACAGGTGT[A/G]AGCCAGTGTGCCTGG | 10277 |
rs773105450 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130254 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 10277 |
rs773134330 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090396 | AAAGTTCTGGAATTA[C/T]AGGCGTGAGCCACCA | 10277 |
rs773160592 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072065 | GACTTGCTGGTGGAC[A/G]GACCTCTCAGCCAAC | 10277 |
rs773183313 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109282 | TCCTGAATCCAGACT[C/T]ATGTTCACCACCGCA | 10277 |
rs773183556 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077016 | TCCCAAAGTGTTGGG[A/C]TTACAGGTGTGAGCT | 10277 |
rs773201779 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161738 | GGGTTTTATATTCAG[-/T]TATTAATAGAAAAGA | 10277 |
rs773215959 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165140 | ACTTGCAGACCAAGT[A/G]TTTGTCTAATCAGTG | 10277 |
rs773227013 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136282 | GTTCAAGACCAGCCT[A/G]GGCAAAATAAGGAAA | 10277 |
rs773233259 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120589 | TGCCTGTAATCCTAT[A/C]ACTTTGAGAGGCCAA | 10277 |
rs773249589 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060552 | GGTTCCAGAAGGTTC[A/G]GATGAGTCCTGAATG | 10277 |
rs773279719 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141192 | CCACATCCTGGTCTC[A/G]GAACCTGTGAATATG | 10277 |
rs773291982 | snp | G/T | 0.00152522 | 0.0275732 | intron-variant | UBE4B | GRCh38.p7 | 1:10130474 | CCTGTTCAGCGGCTT[G/T]ACTGGCTCTTCCATC | 10277 |
rs773293922 | snp | A/C | 1.72588e-05 | 0.00293753 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106518 | CAGCAGCACGGGTCC[A/C]CCCCTACCACCCGCC | 10277 |
rs773311047 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075864 | CGAGACCAGCCTGGG[C/T]GACATAGCAAAACCC | 10277 |
rs773320070 | snp | A/G | 0.000307961 | 0.0124051 | intron-variant | UBE4B | GRCh38.p7 | 1:10107421 | GTGCGTAGATGCTTA[A/G]GAACTAACTTCTATA | 10277 |
rs773334687 | snp | A/G/T | 0.000115416 | 0.00759579 | intron-variant | UBE4B | GRCh38.p7 | 1:10129483 | GCTTGCACATTTTCA[A/G/T]TGAATATATCATAAC | 10277 |
rs773337410 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178184 | ATGAACAATAGTGGA[G/T]TGTTTTTACCATGCT | 10277 |
rs773361650 | snp | C/T | 1.6607e-05 | 0.00288153 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179898 | TTCTTTTCTCAGTGC[C/T]AGAACTGAAAGAGCA | 10277 |
rs773371398 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077860 | CAAGTCCACAGGTCA[-/T]TGCTGTTCCAGACTT | 10277 |
rs773373043 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047426 | GTCCTTAGGAAGGGA[C/G]TCAAGTGGGAGGAGA | 10277 |
rs773412487 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179736 | TTTTTCCCTGCAGAC[A/T]TCCAGTCCCTCCCTC | 10277 |
rs773429909 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176246 | TTGTTTATCCTCATC[C/G]ATTGATAGACATTTG | 10277 |
rs773441645 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067756 | TTGTTGAGATGGAGT[C/G]TCACTCTATGGCCCA | 10277 |
rs773442069 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130744 | AAAATACTTCTCAGG[C/G]CCTGCCATTACCCTG | 10277 |
rs773469281 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10132278 | GGGAGAGGAGAGAAC[A/G]TGGGAAGTAGGCTAG | 10277 |
rs773476962 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144014 | AGGAAATGTAGCTTT[C/T]GGAGATTTAGCAGCC | 10277 |
rs773537927 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088752 | TGACGCAATCATGGC[C/T]CACTGCAAGCTTGAC | 10277 |
rs773558130 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108469 | GGTTGTGTAGGTGAC[-/TT]TGAGCAAGAGAATAT | 10277 |
rs773558973 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083087 | GGTTCCATGTCTTTG[C/G]TATTGTAAATAGTGC | 10277 |
rs773571092 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050226 | ACAGGCATGCACCAC[C/T]ACACTTGGCTAATTT | 10277 |
rs773575953 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042492 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCGGGC | 10277 |
rs773580256 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137859 | CTGCGTAGTCTGTCT[A/C]TGAGAGAAACTGAAT | 10277 |
rs773584652 | in-del | -/CTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146878 | ACCCAAATTTCCCAT[-/CTC]CTGGCCCCAGTCCCT | 10277 |
rs773592909 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034007 | AAGGGCGAGATTTAC[A/G]TGAAGTTAAAGTGTG | 10277 |
rs773600728 | snp | A/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10146969 | CTTCCACAGAAACTG[A/G]TACGGTGCAAGGCCT | 10277 |
rs773602561 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163436 | GCACTTTGGAAGGCC[A/G]AGGCGAGTGGATCAC | 10277 |
rs773613428 | snp | A/G | 3.35121e-05 | 0.00409328 | intron-variant | UBE4B | GRCh38.p7 | 1:10122085 | CAAGCAGGTACGGTC[A/G]TATGAGTTTGCTCTT | 10277 |
rs773624976 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102352 | TGTACATCCTCTGTC[A/G]CATATTTTTCCTTGG | 10277 |
rs773635867 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125718 | TGATCAGTGCTTGCA[C/T]TGTGAAATTTGAAGA | 10277 |
rs773639277 | snp | A/T | 3.33222e-05 | 0.00408167 | intron-variant | UBE4B | GRCh38.p7 | 1:10161105 | CATTTTGCTTCAGGG[A/T]GATGTATGACCATGT | 10277 |
rs773648714 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081629 | GTTTCGCTCTTGTCA[C/T]CTAGGCTGGAGTGTA | 10277 |
rs773667051 | snp | C/T | 1.6989e-05 | 0.00291449 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106217 | ATGAAAGTAGTCCGG[C/T]TCCCACTCCCAGTTT | 10277 |
rs773671082 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069235 | GGTATGCTCTTCCAA[C/T]GATAATGATAACGTC | 10277 |
rs773684035 | snp | C/T | 1.7022e-05 | 0.00291731 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168264 | CCAGAAGCCCTTCCT[C/T]AGACCGGTGAGTAGA | 10277 |
rs773704786 | in-del | -/A | 1.6489e-05 | 0.00287128 | intron-variant | UBE4B | GRCh38.p7 | 1:10129482 | GGCTTGCACATTTTC[-/A]GTGAATATATCATAA | 10277 |
rs773715213 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10081821 | CTCGAACTCCTGACC[C/T]CAGGTGGGCTGCCCG | 10277 |
rs773757624 | in-del | -/T | 1.65671e-05 | 0.00287807 | intron-variant | UBE4B | GRCh38.p7 | 1:10161129 | CCATGTACAATATAA[-/T]TTGCCTTTCCAGCTC | 10277 |
rs773758930 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124439 | GTGGTCCGCCCACCT[C/T]GGCCTCCCAAAATGC | 10277 |
rs773765316 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053218 | CAGTGGCGCGATCTC[A/G]GCTCGCTGCAAGCTC | 10277 |
rs773779085 | in-del | -/CA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148631 | GGTGAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 10277 |
rs773782785 | snp | C/T | 6.80921e-05 | 0.0058345 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106511 | AGAGGCCCAGCAGCA[C/T]GGGTCCACCCCTACC | 10277 |
rs773827691 | snp | A/G | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149257 | TATGTAGAAGATGTT[A/G]CAGAATTTTTATTTT | 10277 |
rs773836808 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120943 | TAACCATATGTTTTT[A/G]AAACTTTTCAAAAAG | 10277 |
rs773843815 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169700 | CTTGTTGGGAAGACT[A/C]AGCGAAAACACACAT | 10277 |
rs773852548 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138102 | ACCACGCCTGGCCAA[-/T]TTTTTTTTTTTTTTT | 10277 |
rs773867431 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127399 | TTTAACGCACTTAGA[G/T]CAGGCATACATTGTG | 10277 |
rs773871405 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126029 | TAGAGGGCCAAGCGC[A/G]GTAGCTCATGCCTGT | 10277 |
rs773878398 | snp | C/T | 8.25062e-05 | 0.00642233 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072060 | TGCACGACTTGCTGG[C/T]GGACAGACCTCTCAG | 10277 |
rs773899176 | snp | G/T | 3.29473e-05 | 0.00405864 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095540 | CCTTGAAACGCAATC[G/T]CAGTCTCTCTCACGT | 10277 |
rs773900718 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112816 | ACACTTAACGCTTGT[A/G]TTAGTGAAACTGGCC | 10277 |
rs773926485 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114719 | AAATACAAAAATTAG[C/T]TGTACATGGTGGCGA | 10277 |
rs773941458 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094500 | GTGCAATGGCGCAAT[C/G]TTGGCTCACTGCAAC | 10277 |
rs773944072 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095191 | GTTTGAATTGGTGCA[A/G]GAGAGGTGATGAGGG | 10277 |
rs773945554 | snp | A/C | 1.68795e-05 | 0.00290507 | intron-variant | UBE4B | GRCh38.p7 | 1:10178822 | ATGAGTTCAGAGGCA[A/C]GTGGACTCGTCGTTT | 10277 |
rs773960099 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156029 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs773992195 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149545 | TAATAGTTAAATATG[C/T]GTTTCTGAGCAACAG | 10277 |
rs773992737 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10047174 | CCAGCTTCCAGATTC[C/T]GTGTATTAGTTAGGA | 10277 |
rs773999476 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161249 | ATGAAGTGCAGGAAG[A/G]GATGAAGAACAAAGA | 10277 |
rs774032466 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123309 | GGTGACGGGTGTCTG[C/T]AATCCCAGCTACTTG | 10277 |
rs774042914 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137982 | CTCTGTTGCCCAGGC[A/T]GGAGTGCAGTGGTAC | 10277 |
rs774053507 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034259 | AGTTATATTCTGGTA[C/G]TTAATAGACCACTAA | 10277 |
rs774053634 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171452 | TTCCTTTGAGTGTGA[A/G]GAGCAGATTTGGGCT | 10277 |
rs774060515 | snp | G/T | 1.65932e-05 | 0.00288034 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151341 | ATACTCTCCCCAGGC[G/T]CTTTATGAGCCCTGT | 10277 |
rs774063026 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138405 | CCTGGCCCAATTTTT[-/T]GTATTTTTTGTAGAG | 10277 |
rs774075678 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147963 | CCGGGTGCGGTGGCT[C/T]ACGCCTATAATCCCA | 10277 |
rs774086286 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046428 | GGCTCTGCTGTCCCC[C/T]ATACAGTGGTGGAGA | 10277 |
rs774105642 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039470 | AATCTCTCTCTGTTG[C/T]CCAGGCTGGAGTGAA | 10277 |
rs774128689 | snp | A/G | 4.9675e-05 | 0.00498348 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103070 | TTCTCTTTCTGCACA[A/G]TTTAAGCAGAACCCA | 10277 |
rs774144479 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130361 | GCTGGGATTACAGGC[G/T]TGAGCCACCATGCCT | 10277 |
rs774178126 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169844 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 10277 |
rs774182138 | snp | C/T | 4.96069e-05 | 0.00498006 | intron-variant | UBE4B | GRCh38.p7 | 1:10105479 | AACCTGTGTTCGAAC[C/T]GTGTGTAACCTGTTC | 10277 |
rs774197257 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063539 | TGTCCCTTTCCTATG[C/T]CCATTGCGCAGGCTT | 10277 |
rs774215067 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109199 | GTGAGGAAGTGGCAG[A/G]GGGAACGGGGGGGCC | 10277 |
rs774227226 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060333 | CTGGGCTACAAACCT[A/G]TACTGCATGTAACTA | 10277 |
rs774240122 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118316 | GTGGAAGCGAAATGA[A/G]TGGGCATGTCTCCAA | 10277 |
rs774266830 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164171 | CATGGTGAAACCCAG[C/T]GTCTACTAAAAATAC | 10277 |
rs774301506 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107806 | TGGTCTCGAACTCCT[C/G]ACCTCAAGTGATCTG | 10277 |
rs774320415 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064392 | TGCTGATCGCATCTC[C/T]GAGGAATTGTAGTAT | 10277 |
rs774331008 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086996 | CTTTTTTAGTACTTA[A/G]GTATGCTAAAAGTGG | 10277 |
rs774331585 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174946 | GCAGTATCTTAGTTT[C/G]CTTTGGTATGTCTTA | 10277 |
rs774335697 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143015 | CAGGAGGCTGAGGTA[C/T]GAGAATTATTTGAAC | 10277 |
rs774346685 | snp | C/T | 0.000181517 | 0.00952499 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132437 | GGCTGCTCTCAGTTA[C/T]ATGGCGGCTGTCGTC | 10277 |
rs774348005 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10161539 | TTTTTAATTTTAAAG[G/T]GCTTTTTTGGAGATG | 10277 |
rs774365877 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122727 | TTGGGAAAGTAAGCA[C/T]TTTGCCTTTAGCAAC | 10277 |
rs774367857 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110068 | TTTCTCATTGATCTT[C/G]CCAGAATTTTTTTAC | 10277 |
rs774373494 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156406 | CACCACACCCAGCTA[A/T]TTTTTGTGGTTTTTG | 10277 |
rs774391546 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137141 | CTGCATGCTCACCAC[C/T]TCTCTATTCTGCCTA | 10277 |
rs774392667 | snp | C/T | 8.25185e-05 | 0.0064228 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145004 | CTGGCAACTAGACAC[C/T]GCGAAATGCTGAAGC | 10277 |
rs774420830 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111245 | CGCGCTACACACACA[A/C]CCCCACACCAAGCAT | 10277 |
rs774441004 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166381 | GTGTGACAGCCTCAC[A/G]GTTTGGAAAGACAAA | 10277 |
rs774446492 | snp | C/T | 9.88875e-05 | 0.00703093 | intron-variant | UBE4B | GRCh38.p7 | 1:10137222 | TATGTGCCATGATAC[C/T]GTGTCCTGGGATTGC | 10277 |
rs774459024 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141485 | ACCATCCCTGCTGAC[C/T]CCTTTTAGACTTCCA | 10277 |
rs774468736 | snp | C/T | 1.68233e-05 | 0.00290023 | intron-variant, downstream-variant-500B, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171132 | TATTATCCTGTGATT[C/T]CCTAGGAGCTTGGAC | 10277 |
rs774481002 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063263 | ATAGAGAGTGAGACC[C/T]TATCTCAAAAAAACA | 10277 |
rs774512550 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054059 | GTAGTAATTAGAAAT[A/G]TTAGATTTTTTTTAA | 10277 |
rs774516669 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | UBE4B | GRCh38.p7 | 1:10146933 | TAGCTACTGACTGAT[C/T]TTTGGGTGGGGACAT | 10277 |
rs774520660 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130501 | CATCTTCTGCCTAGG[C/T]TGCTTCTTTGCGGTT | 10277 |
rs774544760 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078381 | TGGTCATGGGAATGC[A/C]AAGATGAGTGAGACT | 10277 |
rs774545937 | snp | C/T | 1.67598e-05 | 0.00289476 | intron-variant | UBE4B | GRCh38.p7 | 1:10072025 | TTTCCCCTCATGTTG[C/T]AGATTCGACGGAGGC | 10277 |
rs774562120 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128330 | TGTGCCATTATTGAT[A/G]CTTGCATAATAACGA | 10277 |
rs774569943 | snp | C/T | 1.64727e-05 | 0.00286986 | intron-variant | UBE4B | GRCh38.p7 | 1:10130630 | ATGTAAGTATAGTGG[C/T]TACTTGTACTTTGCT | 10277 |
rs774572275 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077349 | TGTGTCCAAATTTCC[C/T]TCTTATGACAGCCAC | 10277 |
rs774596563 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121802 | CAAAAAGTGATTACT[A/G]TTGGTAAGAAGGGTT | 10277 |
rs774602422 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051230 | AAAGTACTTAATCTT[A/T]CTGAGCCTCAGTTTC | 10277 |
rs774623536 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134021 | CACCACTGCACTACA[A/G]CCTGGGCAACAGAGT | 10277 |
rs774660133 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154587 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 10277 |
rs774675274 | in-del | -/ATA | 4.95569e-05 | 0.00497755 | cds-indel, upstream-variant-2KB, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10101190 | AGCGGAGCCTCAGTG[-/ATA]ATAAGGTTGGTAAGC | 10277 |
rs774680527 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084317 | TTGAAAGCCTTCCTC[A/G]TCTCCTTATTTCCAA | 10277 |
rs774682048 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055789 | GCTGGGTGTGGTAGC[A/G]CGTGCCCGTAGTCCC | 10277 |
rs774696643 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069846 | AGTGTACGGATGTCC[A/T]TTGTGCAGAAACTGA | 10277 |
rs774718160 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172900 | CTTTTCTGTGTTTAG[-/A]AATACTCACCATTGT | 10277 |
rs774747080 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072132 | GGGGCCTCCCATAGC[A/G]GCATCAGCCCCAGGA | 10277 |
rs774764688 | snp | G/T | 1.81122e-05 | 0.00300928 | intron-variant | UBE4B | GRCh38.p7 | 1:10132531 | TCAAATTCATTCATC[G/T]GACCCAGATTTAGTC | 10277 |
rs774771590 | snp | C/G | 1.66327e-05 | 0.00288376 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179454 | ACAGACCCCGTGCGG[C/G]TGCCCTCTGGCACCA | 10277 |
rs774773556 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091866 | CGTCTTGGCCTCTCA[A/G]AAGTGCTGAGATTAC | 10277 |
rs774784399 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069315 | TCATTTATTCAGCAG[A/G]TATTTAGAGAGTACC | 10277 |
rs774787397 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115667 | CCTTTAACGAGAGGG[A/G]TACATTCTGAGAAAT | 10277 |
rs774789457 | snp | A/G/T | 3.33429e-05 | 0.00408296 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168245 | ACATCCTCACGAAGC[A/G/T]GGTCCAGAAGCCCTT | 10277 |
rs774823094 | in-del | -/AAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152262 | GACTCCGTCTCAAAT[-/AAT]AATAATAATAATAAT | 10277 |
rs774833066 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102566 | GCCAGGCCCGCAACC[A/G]CGCCTGGCTAATTTT | 10277 |
rs774839148 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098871 | GACTGCTATTTCTTC[C/T]TGTATTTAGCAGTGC | 10277 |
rs774852956 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137116 | CCCTACGGAGTGCTT[C/G]TTTCTCACCCTGCAT | 10277 |
rs774885904 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090629 | GAGATGATGTCTCAC[C/T]ATGTTGTTTAAGCTG | 10277 |
rs774898387 | snp | C/T | 1.6759e-05 | 0.00289469 | intron-variant | UBE4B | GRCh38.p7 | 1:10119663 | GCAGAGAGCCCTAGC[C/T]GTCAGTGGACATCAG | 10277 |
rs774930129 | in-del | -/G | 3.39928e-05 | 0.00412253 | intron-variant | UBE4B | GRCh38.p7 | 1:10126778 | TATATTTCTGATTTT[-/G]TTTTTTTTCTTATAG | 10277 |
rs774939638 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115850 | CTAGGCAATTAGATG[C/T]TTATGCCAATTATGG | 10277 |
rs774939987 | in-del | -/TAATTCCATGTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176384 | TTGTTGGTCATGTGG[-/TAATTCCATGTT]TAATTCCATGTTTAA | 10277 |
rs774941536 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128817 | TGCTAAATTATGTTT[A/G]TGTCCCTAAAAAGTG | 10277 |
rs774947075 | snp | A/G | 3.70576e-05 | 0.00430435 | intron-variant | UBE4B | GRCh38.p7 | 1:10178606 | TTTTTTCCACCTGAC[A/G]TACATTTACGTCTCA | 10277 |
rs774949472 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070534 | TCCCACCAAGGATAA[C/T]CATTATCCAAACTAA | 10277 |
rs775006404 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157896 | AGATTTAGGGATGAT[A/G]GACACATTGGTGTTT | 10277 |
rs775011875 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158838 | ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 10277 |
rs775019058 | snp | C/G | 4.9423e-05 | 0.00497082 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105681 | TGCTAAACACTGGCT[C/G]CAATCCAGGAACAAG | 10277 |
rs775020977 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10122019 | TAGGAATCTCCCATA[C/T]GGCTTCATTCAGGAA | 10277 |
rs775063500 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083507 | TAAGAATGCTATCCA[C/T]AATGACAATGAAATT | 10277 |
rs775124123 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037627 | CAATGGCATGATCTT[A/G]GCTCACTGCAACCTC | 10277 |
rs775143993 | snp | C/T | 1.66026e-05 | 0.00288115 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106398 | CTACACTGTCACTCA[C/T]CCATGGGCGTCCTCA | 10277 |
rs775170673 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127728 | GAATTCATTACTGAC[A/G]ATCTGTTCTGTGCTA | 10277 |
rs775172540 | in-del | -/ATC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051071 | GAGTGCAGTGGCATT[-/ATC]ATAGCTCACTGCAGC | 10277 |
rs775196265 | snp | C/T | 1.65575e-05 | 0.00287724 | intron-variant | UBE4B | GRCh38.p7 | 1:10102936 | TAACCTGCAAATCTT[C/T]TTCTTCACCAGGAGC | 10277 |
rs775269515 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037756 | AGACAGGGTTTCACC[A/G]TGTTGCCCAGGCTGG | 10277 |
rs775280085 | snp | A/C | 1.65143e-05 | 0.00287348 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178739 | AAAATTTAAGCTGCT[A/C]GCCGAGAAAGTGGAG | 10277 |
rs775342634 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097769 | GACCTGAGATCGCAC[C/T]GCTGCACTCCAGCTT | 10277 |
rs775349287 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075566 | GGGCATTCCCTAAAC[A/G]GTTAGTTCTTGCCCG | 10277 |
rs775368374 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142276 | AACTCTTGTGATACC[C/T]GTAGCCATATAGGTC | 10277 |
rs775393409 | snp | C/T | 1.65345e-05 | 0.00287524 | intron-variant | UBE4B | GRCh38.p7 | 1:10158329 | AGAAAATACATATCC[C/T]TCAGTACCTTTGTCT | 10277 |
rs775395422 | snp | A/G | 4.97343e-05 | 0.00498645 | intron-variant | UBE4B | GRCh38.p7 | 1:10179585 | AGGGTGCAGTTTGAG[A/G]TGCAGCGCTGGCGTC | 10277 |
rs775403184 | in-del | -/T | 0.00013312 | 0.00815736 | intron-variant | UBE4B | GRCh38.p7 | 1:10179886 | ATCCTCCTTTTTTTC[-/T]TTTCTCAGTGCCAGA | 10277 |
rs775406556 | snp | C/T | 1.65745e-05 | 0.00287871 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117550 | GATATGCTGAACTAC[C/T]TCATCGAGTGTTTCG | 10277 |
rs775410064 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112108 | CAGTCTGCACAGATC[A/G]GATGCACGTGTAATC | 10277 |
rs775420443 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175619 | TCGCGCCACTGCACT[C/G]CAGCCTGGGCGACAG | 10277 |
rs775421048 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166688 | CAGCTCTTTGGGAGG[-/T]TGAAGTGGATGGATC | 10277 |
rs775431889 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055217 | GGGAGAATTTTAATG[A/C]ATGCCAATTGGAACA | 10277 |
rs775434215 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096474 | CGATGGCTCATGCCT[A/G]TAATCCTAGCACTTT | 10277 |
rs775465631 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040794 | GGCTAATTTTTTTGT[A/G]TTTTTATTAGAGACG | 10277 |
rs775500153 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099542 | AGTAATATATTACTT[C/T]TCCCCAAGTTGATCT | 10277 |
rs775504940 | snp | A/C | 2.93975e-05 | 0.00383378 | intron-variant | UBE4B | GRCh38.p7 | 1:10135226 | TCATTAAAACACTGC[A/C]CTCTTGTCTGTGTGC | 10277 |
rs775512022 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085346 | TTGTCACCTCGTGGC[A/C]TCAGGCCTCTTGACT | 10277 |
rs775520461 | snp | A/G | 1.66949e-05 | 0.00288915 | intron-variant | UBE4B | GRCh38.p7 | 1:10158532 | TCTTGCAAATCGCAG[A/G]TAGGATTGCAGCTTA | 10277 |
rs775525312 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149706 | TAACTGGTATTGTAG[A/G]GTTTTAATTTTTTTT | 10277 |
rs775526632 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156667 | TTCCTCTTGTAGGCT[A/C]TCCTTATGTCAACAC | 10277 |
rs775532340 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042326 | AACGTTGCTGTATGG[A/T]GCTTCGTCCTAGTGG | 10277 |
rs775534328 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077903 | ATTTCTTCATGTTTT[-/A]CTGCATTGTTATGTG | 10277 |
rs775546042 | in-del | -/GACACA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111044 | TCTTTCTCTGTCTCT[-/GACACA]CACACACACACACAC | 10277 |
rs775553377 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086262 | AGGCATGAGCCACTG[C/T]GCCTGGCCAATTTTT | 10277 |
rs775560853 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163222 | AAGCATGTACCACCA[C/T]GCTTGGCTAATTAAA | 10277 |
rs775573425 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161205 | GACGTTTTTGCTCGA[C/T]GAAAGTCTGGAGTCT | 10277 |
rs775600067 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10114955 | TCTGGCGAGGGCTTT[C/G]TAGGTGGCTTAGTTA | 10277 |
rs775639481 | snp | A/G | 8.27767e-05 | 0.00643284 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168223 | ACCGAAACCGTGGAC[A/G]TGTTCCACATCCTCA | 10277 |
rs775679079 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10122130 | GAGAGCCTCTATGTC[A/G]AGGCTAATTTCTGAC | 10277 |
rs775684891 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105670 | CAGAAATCTCTTGCT[A/G]AACACTGGCTCCAAT | 10277 |
rs775689518 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169972 | GTGAGCCGAGATCAC[A/G]CCACTCCAACCTGGG | 10277 |
rs775692397 | snp | C/T | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144986 | CAATGGAAAGATTCC[C/T]CACTGGCAACTAGAC | 10277 |
rs775708512 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065541 | GGCCAGTTAAATGTG[A/C]ACACAATTGAATGTG | 10277 |
rs775710309 | snp | C/T | 1.65949e-05 | 0.00288048 | intron-variant | UBE4B | GRCh38.p7 | 1:10119645 | CGTGCTTGACATTAG[C/T]AGGCAGAGAGCCCTA | 10277 |
rs775720844 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131441 | AGTGAGCCAAGATCA[C/T]GCCACTGCACATCAG | 10277 |
rs775745471 | in-del | -/TTG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067729 | CTCCCATCTCAGTAT[-/TTG]TTGTTGTTGTTGTTG | 10277 |
rs775752412 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153113 | TCCTTCAGTTTTCCA[A/G]TTCTCCTGCAGCACC | 10277 |
rs775766500 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123004 | AGAATAAAAATTCCA[A/G]TTAGTGTTGTGTATT | 10277 |
rs775798148 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079971 | CAGGGGCCTCCAGGG[C/G]CTCACTGTTTAGCAT | 10277 |
rs775798313 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064684 | CATCTCTGTGCCTAC[C/T]GTGTACTGCTGTACA | 10277 |
rs775819035 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058662 | AGCCCACCAGCTGCC[A/G]CCTGCAGGTGGGCAA | 10277 |
rs775834087 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058144 | GTGCTTGGGTAAAAG[C/T]ACTAGATACTTTAGG | 10277 |
rs775837082 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119381 | ACAGTTACTGTAGCT[C/T]GTTCACTAAGAATAA | 10277 |
rs775878556 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166551 | CCAGCACTTTGGGAG[C/G]CCTAGGTGGGCAGAT | 10277 |
rs775888771 | snp | C/G | 6.58946e-05 | 0.0057396 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095509 | TCAGTTCTCTCAGCA[C/G]CTCGCCCTCTAATAG | 10277 |
rs775891937 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179779 | CCTTCTGGAGTCTTC[A/G]GCTCAATGAGGGAAA | 10277 |
rs775899732 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10036250 | TCAGTCCTTGAGGAA[-/G]GTGTAACTTTTTTTT | 10277 |
rs775903336 | snp | A/G | 0.000115532 | 0.0075995 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149229 | CAAGGTATTTGCAGC[A/G]TTGCCTGAGTTTTAT | 10277 |
rs775921159 | snp | A/G | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179943 | TGAGAGAGAAACAGA[A/G]CAGCGATCACTAAAC | 10277 |
rs775927157 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135273 | ATTGTTACCACCTCA[C/G]CATAAAATGAACTTA | 10277 |
rs775930352 | snp | A/G | 3.31082e-05 | 0.00406854 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180001 | ACAGCCAAGGCCAAC[A/G]AGGCAAGCAGAAGCA | 10277 |
rs775979735 | snp | G/T | 3.31164e-05 | 0.00406904 | intron-variant | UBE4B | GRCh38.p7 | 1:10158499 | TGAGTATGGGGCCCC[G/T]CGTGTCACAACTTGC | 10277 |
rs776019872 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076463 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10277 |
rs776029164 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078621 | TGCTTGTCTTCTCTT[C/T]GATGTTTGCCTATCA | 10277 |
rs776072724 | in-del | -/ATAG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126306 | TCCGTCTCAATATAG[-/ATAG]ATAGATAGATAGATA | 10277 |
rs776086982 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167208 | ACTTCGGGAGGCCAA[C/G]GCAGGCTGATCACCT | 10277 |
rs776093046 | snp | A/G/T | 3.31182e-05 | 0.00406918 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135089 | AACAGTTGATCCCAC[A/G/T]TATATTTTTCACCCA | 10277 |
rs776094664 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044148 | GGTGCCAGGTTCAAG[C/T]GATTCTCGTGTCTCA | 10277 |
rs776102839 | snp | A/C/T | 3.30138e-05 | 0.00406276 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10132442 | CTCTCAGTTACATGG[A/C/T]GGCTGTCGTCAATGC | 10277 |
rs776106402 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041091 | TCCTCTCCTTTTGTT[C/T]ATTGTAGACAAGAGA | 10277 |
rs776117354 | in-del | -/TC | 0.00011971 | 0.00773568 | intron-variant | UBE4B | GRCh38.p7 | 1:10072466 | CAGGTTTAGGTATTA[-/TC]TCTGATGACAAGATG | 10277 |
rs776131038 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128935 | GTTATGTTTTTAAAT[A/G]TGTTTTGAATTTGAT | 10277 |
rs776157772 | snp | C/G | 1.79929e-05 | 0.00299935 | intron-variant | UBE4B | GRCh38.p7 | 1:10132527 | TTTGTCAAATTCATT[C/G]ATCTGACCCAGATTT | 10277 |
rs776157937 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119540 | CCAGCAGTCAGCCAG[C/T]TTCTGAGCAACATCC | 10277 |
rs776159851 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146761 | GACCTGGTGGTACTC[A/G]GTGGTTTGCTTGCCA | 10277 |
rs776161247 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117316 | CAGGTGAAACAAGCA[A/G]TCAGGGTGGATCTTG | 10277 |
rs776174736 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165054 | TTGGTGAGCTCAGGT[A/T]TACCAAGGCATTAAA | 10277 |
rs776191078 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134286 | GAGGCCGAGACGGGC[A/G]TATCACCTGAGGTCA | 10277 |
rs776192940 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070207 | TGAACCTGGGAGGGG[A/G]AGGTTGCAGTGAGCC | 10277 |
rs776208917 | in-del | -/AAGT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098895 | GCAGTGCAGTAAAAC[-/AAGT]AAGGATTGGAATGGA | 10277 |
rs776212341 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093033 | CAAATGCAGTATGTT[A/G]CACTATGTGATATAC | 10277 |
rs776222912 | snp | C/G/T | 3.41229e-05 | 0.00413043 | intron-variant | UBE4B | GRCh38.p7 | 1:10122112 | TCTTGCAAATTTTAG[C/G/T]CTGAGAGCCTCTATG | 10277 |
rs776231321 | snp | C/T | 1.73276e-05 | 0.00294338 | intron-variant | UBE4B | GRCh38.p7 | 1:10071999 | TCTGCTGATTAGTTA[C/T]AGAATGCCCTTTTCC | 10277 |
rs776242768 | snp | A/G | 1.65236e-05 | 0.00287429 | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179972 | ACCGTTCCGCCGCCC[A/G]CCCTCTGCTAGACAC | 10277 |
rs776251203 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058854 | CAGATGTGGCTCCCA[G/T]TAGTGATGACTTGGT | 10277 |
rs776253868 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054024 | CATTTTCCTTCATCA[A/G]ATCTTTTTTTGTTGT | 10277 |
rs776274308 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | UBE4B | GRCh38.p7 | 1:10130480 | CAGCGGCTTGACTGG[C/T]TCTTCCATCTTCTGC | 10277 |
rs776275736 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126839 | CTTGCTGCCAAAGAG[C/T]GCTCCCTCGACAGTG | 10277 |
rs776276915 | in-del | -/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032650 | GCGGGCCCCCGGGCC[-/G]CGGGCCAGCGCCACC | 10277 |
rs776319227 | snp | G/T | 1.76883e-05 | 0.00297386 | intron-variant | UBE4B | GRCh38.p7 | 1:10178859 | TGATTTCTTTTGAGT[G/T]AACTGGAAATCGATA | 10277 |
rs776409767 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048890 | AAATGTGGTGAGCTT[A/G]TCTTTTTCTGTTTTA | 10277 |
rs776417451 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127951 | AATGCTGGGAAATTA[A/G]AAGGTGAAACCAGAA | 10277 |
rs776445273 | snp | A/C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179826 | CCATTTATACAGAGC[A/C/G]ACAAGCATCCTCTCT | 10277 |
rs776452868 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172157 | CCGTGGGTCTCCTGT[A/G]AGCAGATCTGTCTGT | 10277 |
rs776462488 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097881 | AGCATTTGTCCTTAT[A/T]TTTTTTGGAGACGGA | 10277 |
rs776463087 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10050116 | CTTGCTCTTGTCACC[C/T]AGGCTGGAGTGCAGT | 10277 |
rs776476371 | snp | A/C/T | 4.942e-05 | 0.00497071 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171224 | CCTGAAAGTTGAAAA[A/C/T]CCTGAGAAATACGGC | 10277 |
rs776476619 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117038 | ATGGTAGAAGTCACA[A/G]AGATGAGGGCTATTT | 10277 |
rs776482412 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063196 | TCGCTTGAACCCAGG[A/G]GGCAGAGGTTGCAGT | 10277 |
rs776500290 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10141051 | GCCCTACATAGAAGT[A/G]TATCAGCATTTTCTT | 10277 |
rs776532939 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130581 | CTCTCTTACTTAGGG[A/G]CTTTCTTTAGCTTCT | 10277 |
rs776554925 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10101051 | CACCCAGCAGCTACA[A/G]TGACATTGTGCGGAT | 10277 |
rs776558206 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085627 | ACACATCTTTATAAC[-/T]TTAATGCAACTGTAA | 10277 |
rs776558973 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117592 | ATAGAGGAAAAAAAA[A/G]CACCAAAGGTAATAT | 10277 |
rs776571840 | snp | C/T | 1.66776e-05 | 0.00288765 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179435 | TCTGATGGACACCCT[C/T]ATGACAGACCCCGTG | 10277 |
rs776583824 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049893 | AAAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10277 |
rs776655886 | snp | C/T | 0.00064683 | 0.0179721 | intron-variant, synonymous-codon | UBE4B | GRCh38.p7 | 1:10107255 | CTCCTTCCTCTTCCT[C/T]GCACTTTCTGGGGAC | 10277 |
rs776664179 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091321 | TGAAGACAAGGGAGT[A/G]TGTGAGGTTTGAAAA | 10277 |
rs776672807 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135943 | CTCAATAATTCTACT[C/T]TTCAGGTTATATTCC | 10277 |
rs776697084 | snp | A/G | 1.71873e-05 | 0.00293144 | intron-variant | UBE4B | GRCh38.p7 | 1:10151595 | GTGTAGCACATGGCA[A/G]GCCAACTTAGGTAAG | 10277 |
rs776718140 | snp | A/G | 1.65477e-05 | 0.00287638 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179923 | AGAGCAGATTCAGGC[A/G]TGGATGAGAGAGAAA | 10277 |
rs776729931 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108242 | GAGCTCAGTCTGGGC[A/G]ATCCATCGAAGAACA | 10277 |
rs776779503 | in-del | -/GAT | | | intron-variant, cds-indel | UBE4B | GRCh38.p7 | 1:10107298 | GAAGATGAAGAAGAA[-/GAT]GATGATGATGGTGAT | 10277 |
rs776780043 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113863 | TGAGGTCAGGAGATC[A/G]AGATCATCCTGGCCA | 10277 |
rs776782101 | snp | A/C | 3.35604e-05 | 0.00409623 | intron-variant | UBE4B | GRCh38.p7 | 1:10168105 | ATGACCAGGACCGAG[A/C]CTTACTCAGCGTCTG | 10277 |
rs776799858 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155728 | TATTCTAGCTTAGAA[A/C]ATGCTCAAGTTAGGC | 10277 |
rs776814203 | in-del | -/AG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10138282 | TTTTGTATTTTTAGT[-/AG]AGACGGGGTTTCACC | 10277 |
rs776821025 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033593 | CCTGATAGACACCTT[C/T]CACTCTCCTTCCTCC | 10277 |
rs776828717 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080255 | TGAAACCCTGTCTCT[A/G]CTAAAAATACAAAAA | 10277 |
rs776844534 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067504 | AAGTAAACAATGAGA[A/G]AAATGTTTAATCATA | 10277 |
rs776848144 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10053775 | CTCACTTGCAGCCTC[G/T]ACCTTTCGGGCTCAA | 10277 |
rs776857427 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143214 | TTCGAGATCAGCCTG[C/G]CCAACATGTTGAAAC | 10277 |
rs776859165 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074225 | TTCTTGTTATGCACA[A/G]ATTGTCCCTGCTGCT | 10277 |
rs776863634 | snp | C/G | 1.64895e-05 | 0.00287132 | intron-variant | UBE4B | GRCh38.p7 | 1:10105501 | AACCTGTTCTTTGTT[C/G]TGCCTTTCCAACAGT | 10277 |
rs776869999 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103747 | GCAATTCTCCAGCCT[C/T]AGCCTCCCGAGTTGG | 10277 |
rs776871961 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137742 | CATTTTTTCCTGTGT[A/G]CTAACACCAACAAAC | 10277 |
rs776888653 | in-del | -/AG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10067069 | TATTAAACTTATAAC[-/AG]TGTTTTGTGGGTGTT | 10277 |
rs776899566 | snp | A/G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10041573 | CTTCTGACCTCAGGC[A/G/T]ATCCCCCCGCCTCGG | 10277 |
rs776916303 | in-del | -/TCG | 1.70319e-05 | 0.00291816 | intron-variant | UBE4B | GRCh38.p7 | 1:10178829 | CAGAGGCAAGTGGAC[-/TCG]TCGTTTTCATGCTGA | 10277 |
rs776977489 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137156 | CTCTCTATTCTGCCT[A/G]GTTGCCGTCGCTATA | 10277 |
rs776981560 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100370 | TGCCCAGGCTGGGAT[A/C]CAGTGGTTATTCACA | 10277 |
rs776997195 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147759 | ATACCCACCTAATTC[A/C]GAGAGTGAGCTAAGA | 10277 |
rs777007475 | snp | C/T | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130769 | ACCCTGGAAAACACT[C/T]GTGTGGTTAGCCAAT | 10277 |
rs777031955 | snp | C/T | 1.67184e-05 | 0.00289118 | intron-variant | UBE4B | GRCh38.p7 | 1:10072251 | GGGACTCTTTTGTAA[C/T]TCTTCTTAGCTTTTT | 10277 |
rs777033482 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154293 | CCGGGTGACGCATGC[A/G]TGTAATCCCAGCAAC | 10277 |
rs777041571 | snp | A/C | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032612 | TCACAGAAAAGCAGG[A/C]GATTGGGAACAACGG | 10277 |
rs777063614 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112772 | CAGTTTGAATCTAAA[A/G]ATTCTTGTAAATCAG | 10277 |
rs777101806 | snp | A/C | 1.66863e-05 | 0.0028884 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171379 | CTGGCAGATTTGGAG[A/C]TAATAACCACAGTGG | 10277 |
rs777103674 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174238 | ATCTCTACTAAAAAT[A/T]CAAAAATTAGCCGGG | 10277 |
rs777104498 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169406 | CACTATTGCCACTCC[C/T]TGGCCTGGGGACAAC | 10277 |
rs777104550 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072154 | GCCCCAGGACCCTCT[C/G]AGAGTCTTGGTCTCA | 10277 |
rs777130960 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124097 | ATCATTTTGAAGTGT[A/G]CAATTCAGTGGCATT | 10277 |
rs777149061 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044897 | CTGTGCCCTTTATTT[C/T]TATTATTATTATATT | 10277 |
rs777157227 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049481 | CAGACGCAATGATGC[A/C]TGCCTGCAATCCCTG | 10277 |
rs777198796 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10149105 | AATGAAATACTTATC[C/T]GATGGTAATGTAATA | 10277 |
rs777201319 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076523 | TGCTGAGATTACACA[C/T]GTGAGCTACCACGCC | 10277 |
rs777211373 | snp | A/C/G | 0.000148298 | 0.00860986 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072117 | GAGGGAGAACCCTCC[A/C/G]GGGCCTCCCATAGCG | 10277 |
rs777224583 | snp | A/G | 1.6476e-05 | 0.00287014 | intron-variant | UBE4B | GRCh38.p7 | 1:10147093 | CCGCATATCCCGAGT[A/G]AGTGTGCTTCTTCCT | 10277 |
rs777263446 | in-del | -/GA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155065 | TCACTGTGGCTTCAG[-/GA]GAGAGAGAGAGAGAG | 10277 |
rs777269375 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135437 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 10277 |
rs777281743 | snp | A/G | 3.30017e-05 | 0.00406199 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10149216 | ATTCAGATGTCCCCA[A/G]GGTATTTGCAGCGTT | 10277 |
rs777293406 | snp | A/C/T | 3.33769e-05 | 0.00408504 | intron-variant | UBE4B | GRCh38.p7 | 1:10179860 | GAAGAGCCCTCCCAT[A/C/T]TGGGGCATTAATCCT | 10277 |
rs777322737 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10123229 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 10277 |
rs777364204 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040809 | ATTTTTATTAGAGAC[A/G]GGATTTCTCCATGTT | 10277 |
rs777375541 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121190 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 10277 |
rs777398196 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100211 | AGCCAGGATGGTCTC[C/G]ATTTCCTGACCTTGT | 10277 |
rs777413135 | snp | C/G/T | 3.29453e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130568 | GGAGCTGCAGAGACT[C/G/T]TCTTACTTAGGGGCT | 10277 |
rs777415891 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162726 | TTTATGATTCAGCCT[A/G]TCACCCAGGGAGTGA | 10277 |
rs777427681 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088183 | CCAAGGAGCAGTCCT[C/G]GTCTACTGACTCCAG | 10277 |
rs777431875 | snp | A/G | 0.000363408 | 0.0134749 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179537 | CTTCAACCGGCAGAC[A/G]CTGACAGAGAGCATG | 10277 |
rs777440758 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055012 | GCTGGGCTTGAACTC[C/T]GGACCTCAGGGGATC | 10277 |
rs777446263 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048384 | TCTTGGGGGAGGTTG[A/G]GGTTAGGGATACTAA | 10277 |
rs777446876 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046426 | GGGGCTCTGCTGTCC[C/G]CCATACAGTGGTGGA | 10277 |
rs777471519 | snp | G/T | 0.000162219 | 0.00900462 | intron-variant | UBE4B | GRCh38.p7 | 1:10107184 | CGTCTTGTTTTTTCT[G/T]TGTTCTCTGATGGCC | 10277 |
rs777477928 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061623 | TAAGATTTTTTGGGG[C/T]AAGGGATCTCCTTGA | 10277 |
rs777516416 | snp | C/T | 1.66696e-05 | 0.00288696 | intron-variant | UBE4B | GRCh38.p7 | 1:10102904 | GAAACACCTAACTCA[C/T]ACCTCTTATTTGAAA | 10277 |
rs777538041 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10169095 | AGAATGTTTGTTCTC[A/G]ACTAGTAAGACCTGG | 10277 |
rs777541667 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153239 | GGCTGGGCACGGTGA[C/T]TCCAGCTAATAATCC | 10277 |
rs777554698 | in-del | -/TC | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171027 | AGCACCTGTAAGGAT[-/TC]TTTGAAGATTAATCC | 10277 |
rs777561093 | snp | C/G | 1.66813e-05 | 0.00288797 | intron-variant | UBE4B | GRCh38.p7 | 1:10121952 | GTCCCTAATGTTCAT[C/G]GGTCCACAGGTCCTT | 10277 |
rs777576346 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100720 | CCACCACGCCTGACT[A/G]ATTTTATATTTTTAG | 10277 |
rs777585003 | snp | A/G | 1.65888e-05 | 0.00287996 | intron-variant | UBE4B | GRCh38.p7 | 1:10145084 | ACCAGCCTCATAGTG[A/G]TAATTTTCCCAACAG | 10277 |
rs777596249 | snp | A/G | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117497 | GTAATTGGGATTCCT[A/G]CAGTGACCATTTCAC | 10277 |
rs777619993 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10093655 | TTGTTTTCACTACAA[C/T]GGGTAACTCAAGTTT | 10277 |
rs777622183 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10155147 | ACAGAACTGGGCCTG[C/T]TGCCTATAAGACGAG | 10277 |
rs777623042 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10076165 | GGAAGTTAGACATAG[A/G]TCTAATGGGTAGATT | 10277 |
rs777637139 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131777 | CCAACATGGTGAAAC[A/C]CCATCTCTACTAAAA | 10277 |
rs777644646 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10129392 | TGATCTTATTTCTAG[A/G]CACTAGGTGAGCTCT | 10277 |
rs777653966 | snp | A/G | 1.71478e-05 | 0.00292807 | intron-variant | UBE4B | GRCh38.p7 | 1:10033738 | ATTAGTTGGCAACTC[A/G]TTAGCGCTTTGGACA | 10277 |
rs777665484 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068513 | TGCCACCATACCTGG[A/C]TAATTTTTGGTATTT | 10277 |
rs777675873 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10142855 | GCTTGCCTGGTGTAT[C/G]GCAGCACTTTGGGAG | 10277 |
rs777677614 | snp | C/G | 1.79754e-05 | 0.0029979 | intron-variant | UBE4B | GRCh38.p7 | 1:10106183 | TTCTTTCCTCCCTTT[C/G]TCAACTAATTTAGCC | 10277 |
rs777705951 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056836 | GGACTGCTTCATTCA[A/T]TTATTCATGAGACAA | 10277 |
rs777724808 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096272 | CTTCGTACGGATCAA[-/G]GTGTCTTGAAAGAGC | 10277 |
rs777725054 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10131126 | TTAGTTTGCACACAC[C/G]CTCACTGACTTGCTT | 10277 |
rs777726502 | snp | A/T | 3.38083e-05 | 0.00411133 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10144958 | TGTAGAAGATTTGAA[A/T]AATAATGAAAGCCAA | 10277 |
rs777732913 | snp | C/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031332 | TCCACCCGCCTTGGC[C/T]TCCCAAAGGGCTGGG | 10277 |
rs777746019 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112295 | TTCAATATGACATAT[C/T]TCCAAGATTTTAGGA | 10277 |
rs777814190 | snp | C/T | 1.65894e-05 | 0.00288 | intron-variant | UBE4B | GRCh38.p7 | 1:10149177 | GTCCTTTTTTTCTCT[C/T]TGACAGTATAACACT | 10277 |
rs777844385 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134690 | TGTTTGAAAGTTCAG[C/T]CTGCTTTCTTACAAA | 10277 |
rs777862902 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166763 | ACCCCAATCTTTACC[-/AA]AAATACAAAAATTAG | 10277 |
rs777871255 | snp | A/G | 2.55021e-05 | 0.00357077 | intron-variant | UBE4B | GRCh38.p7 | 1:10132323 | AAAAAGGAATCATGT[A/G]CAAAATAGTTTTAAT | 10277 |
rs777899540 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071110 | CAGGATTTCACCATG[G/T]TGGTCAGGCTGTTCT | 10277 |
rs777906682 | snp | C/T | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10145022 | GAAATGCTGAAGCGC[C/T]GTAAAACTCAGCTTA | 10277 |
rs777930202 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091666 | GCCGCAGTGCAGTGG[G/T]GCGATCTTGGCCCAC | 10277 |
rs777934800 | in-del | -/TTTTTTTTTTTTTTTTTTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118876 | AGGCTGGTCTTTTTT[-/TTTTTTTTTTTTTTTTTTT]TTTTTTTTGAGATGG | 10277 |
rs777945500 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10103012 | TCTGTAAGATCTTCC[A/G]TGTCTCTTGGAAGGA | 10277 |
rs777954629 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058328 | AGATTGCAGGGTGAC[C/T]GTGCCATTCTACCCC | 10277 |
rs777955576 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140334 | AAAATATATTTTATG[C/T]GATTTGTGTCTTTTG | 10277 |
rs777958713 | snp | C/G | 3.36939e-05 | 0.00410436 | intron-variant | UBE4B | GRCh38.p7 | 1:10179378 | TTTCAGTCGTGGGCT[C/G]TCAGTAGATTAGAGT | 10277 |
rs777968249 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103717 | CTCACTGCAACTCCC[A/G]CCTCCTGGGTTCAAG | 10277 |
rs777976670 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10070444 | ATCCAGTTAAAATTA[-/A]AAAAAAAAAAAAAAA | 10277 |
rs778006523 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128579 | TTGGGGTTTCCAAAG[A/G]CTTCCCATGTGATCC | 10277 |
rs778011902 | in-del | -/GTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042227 | TCTCACACGGCACTT[-/GTA]GTATCTAGTGGAAAT | 10277 |
rs778022349 | snp | C/T | 0.000148264 | 0.00860872 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105682 | GCTAAACACTGGCTC[C/T]AATCCAGGAACAAGC | 10277 |
rs778042309 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10164047 | ATTATTTTTTAATAG[-/A]AACAGAGTCTTGACC | 10277 |
rs778061362 | snp | C/T | 1.65649e-05 | 0.00287788 | intron-variant | UBE4B | GRCh38.p7 | 1:10072229 | GGTAAGCCCAAGCTT[C/T]ATACCTGGGACTCTT | 10277 |
rs778066832 | snp | A/T | 3.45334e-05 | 0.00415518 | intron-variant | UBE4B | GRCh38.p7 | 1:10151282 | GATGAGTTTCTCAGC[A/T]GTTTCTCAGCGGTCT | 10277 |
rs778096765 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161150 | TTTCCAGCTCCGGGA[A/G]GCAGTTTGTTCGCTA | 10277 |
rs778096873 | snp | A/G | 2.1376e-05 | 0.00326918 | intron-variant | UBE4B | GRCh38.p7 | 1:10135193 | CTGAACTCTGTGAGT[A/G]CTGTGTTCGTGACTC | 10277 |
rs778112938 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063911 | GAAACTGTCTCAATG[-/A]AAAAAAAAAAAAAGA | 10277 |
rs778114691 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040302 | TTTAGTAGAGACGGT[A/G]TTTCACCATATTGGC | 10277 |
rs778115044 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10083734 | AGAAGAGGTTGAAAT[A/C]CTTTGCTTTTTGCTT | 10277 |
rs778135549 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084281 | GCTTAGTAGGAGAGA[G/T]AATACATGTCACTCA | 10277 |
rs778154798 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10127203 | GAAATTTTGTTACTT[A/T]AAAAAAAAAAACCTA | 10277 |
rs778175225 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175994 | TCGCTGTCTAGACCC[C/T]CTTGCCCCAGCCCCT | 10277 |
rs778186245 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088686 | GTATTTTATTATTTT[-/A]TTATTATTTTTGAGA | 10277 |
rs778204367 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10037334 | GCCCGGTAGTCTTGT[A/G]CTTTTAAGTAGAGTA | 10277 |
rs778217487 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057693 | TGAAATCGTGTTACT[C/G]TACTCCAACCTGGCT | 10277 |
rs778241645 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150332 | ATTTAAGCAACTCAA[A/G]TCACATTTTAAAATT | 10277 |
rs778275026 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10077889 | TTGCCATTCCAGATA[C/T]TTCTTCATGTTTTAC | 10277 |
rs778290196 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115601 | ATTCCAAGGTCAATT[A/G]TGTGTAGTTTTCCAA | 10277 |
rs778318101 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097577 | TCACTTTGGGAGGCC[A/G]ACGCAGGTGTTCACT | 10277 |
rs778339850 | snp | C/T | 1.72163e-05 | 0.00293391 | intron-variant | UBE4B | GRCh38.p7 | 1:10105769 | GTTCTCTTTGCACAT[C/T]TTACTGGTAGTAAAA | 10277 |
rs778358174 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139178 | AGGCAGACGGATCAC[C/T]TGAGGTCAGGAGTTG | 10277 |
rs778363412 | snp | A/C | 4.95045e-05 | 0.00497492 | intron-variant | UBE4B | GRCh38.p7 | 1:10126891 | TGGTAAAACTTTGTT[A/C]TTTTTCTTTAACTCA | 10277 |
rs778384074 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10139133 | GGGCACAGTGGCTTA[C/T]GCCTGTAATCCCAAC | 10277 |
rs778385801 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156239 | TTTCATTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs778402260 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10109717 | GTGCAGTGGAGCGAT[C/T]TCGGCTCACTGCAAC | 10277 |
rs778425495 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048380 | CAGTTCTTGGGGGAG[A/G]TTGGGGTTAGGGATA | 10277 |
rs778440955 | in-del | -/AC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10097249 | AAGATATTTAGAGAT[-/AC]AGAGGACAGAGTCCT | 10277 |
rs778472928 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10091316 | GGGCATGAAGACAAG[A/G]GAGTGTGTGAGGTTT | 10277 |
rs778473726 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10062723 | GCATTTTGGGTGAGT[A/G]AGGCAAGTGGATCAC | 10277 |
rs778483680 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165457 | CCATATCAGGGATGG[C/T]GTTAAACATCTCAGT | 10277 |
rs778486730 | snp | A/G | 3.31879e-05 | 0.00407343 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171358 | GTTGGTCTCTCTGTG[A/G]GTTTACTGGCAGATT | 10277 |
rs778541952 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175455 | AGGAGATCGAGACCG[G/T]CCTGGCTAACACGGT | 10277 |
rs778569482 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129022 | TAAAGTTTATGAAAT[-/A]AAATCTTTTTGACAT | 10277 |
rs778571750 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126578 | GTTCACCAAACTCCT[C/T]TTACTTCTGGAGAAT | 10277 |
rs778594873 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110595 | AAAGGTACCGCAGAA[A/G]TTATCCGGAGGAAAA | 10277 |
rs778603092 | snp | A/T | 1.65427e-05 | 0.00287595 | intron-variant | UBE4B | GRCh38.p7 | 1:10145062 | TAGCTAAGTGGAATA[A/T]TTATAGACCAGCCTC | 10277 |
rs778605093 | snp | C/T | 5.00722e-05 | 0.00500336 | intron-variant | UBE4B | GRCh38.p7 | 1:10130468 | CACCGGCCTGTTCAG[C/T]GGCTTGACTGGCTCT | 10277 |
rs778610100 | in-del | -/T | 1.71613e-05 | 0.00292923 | intron-variant | UBE4B | GRCh38.p7 | 1:10072009 | AGTTATAGAATGCCC[-/T]TTTCCCCTCATGTTG | 10277 |
rs778615338 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10048591 | ACAGTCTAGAGAGCA[A/T]GGAATCTGGTGTCCA | 10277 |
rs778632822 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10042158 | GCTCATCAAGTAGCC[C/T]CAAGCTCTTGTAGGG | 10277 |
rs778649556 | snp | C/T | 0.000127499 | 0.0079833 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106566 | CAGACGCCCCTCCTC[C/T]CTGAGGATCTCTCCT | 10277 |
rs778650656 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101821 | CTGGTCTTTTGCTTT[G/T]AAGCAAGTAGATCAT | 10277 |
rs778673227 | snp | A/G | 3.30568e-05 | 0.00406538 | intron-variant | UBE4B | GRCh38.p7 | 1:10119486 | TGTTTGTTTCTTGTC[A/G]TCCTCACTTCCACCT | 10277 |
rs778678858 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10052191 | TCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10277 |
rs778680166 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150532 | GCTACAGCCAGTAAC[C/T]ATGTTTGGTTTTAAA | 10277 |
rs778686193 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082727 | CATGTGCCATGGTGG[C/T]TTGCTGCACCTATCA | 10277 |
rs778705634 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090127 | CCTGTGTGTGTGTGT[G/T]TTTTTTTTTTTAGGC | 10277 |
rs778716631 | snp | A/G | 1.6517e-05 | 0.00287372 | | | GRCh38.p7 | 1:10168188 | ATGAGCGTGTGTCCC[A/G]CTCTTACCTCGCCCT | 10277 |
rs778720798 | snp | C/T | | | | | GRCh38.p7 | 1:10055270 | AGGCCACCTTTTCAT[C/T]ATTTTTTCTTTTCTT | 10277 |
rs778728074 | snp | A/G | 1.64789e-05 | 0.0028704 | | | GRCh38.p7 | 1:10119590 | TACTGCTTTAGTACT[A/G]CAAGGCTCCCTAACA | 10277 |
rs778733607 | snp | C/T | 4.95561e-05 | 0.00497751 | | | GRCh38.p7 | 1:10179973 | CCGTTCCGCCGCCCA[C/T]CCTCTGCTAGACACA | 10277 |
rs778761666 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143745 | AGCAGAAAGGGGAAC[C/T]AGTTGGTTTACTGAA | 10277 |
rs778764120 | snp | C/G | 1.74127e-05 | 0.0029506 | intron-variant | UBE4B | GRCh38.p7 | 1:10132511 | AGACTGCTTTTCGCT[C/G]TTTGTCAAATTCATT | 10277 |
rs778772896 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121284 | CACTTGAACCCGGGA[A/G]GCGGAGGTTGCAGTG | 10277 |
rs778799273 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10177478 | CTGGGTGACAAAGCG[A/G]GACTCCGTCTCAAAA | 10277 |
rs778803907 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034664 | CTTCCCTACAGTATT[A/T]GGAAAGCAGTCATCC | 10277 |
rs778827517 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056406 | TGTGTCAAGTAAACA[C/T]TTTTCATTTGTTCAG | 10277 |
rs778853378 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137068 | GTTATTTTTCCTAGA[C/T]GGCGATCAGCCTCCA | 10277 |
rs778855245 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105635 | TCACAGCCAATTGCT[A/G]CAGCAGCACGGTCAC | 10277 |
rs778856734 | in-del | -/TTTT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082634 | TTAAGAAGGCGACTT[-/TTTT]TTTTTTTTTTTTTTT | 10277 |
rs778864628 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10120155 | CTCAGTCTTCTAAAG[A/G]TAGCAAGTTTTTAAA | 10277 |
rs778871369 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100057 | TGCAGTGGCGCAGTC[C/T]TGGCTCACTGCGAGC | 10277 |
rs778873595 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10065873 | AATCTACATCCTTTT[-/A]AAAAAATAAATGGAA | 10277 |
rs778883385 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100833 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACT | 10277 |
rs778908699 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10126874 | CTTTAAATACCCCCT[C/T]ATGGTAAAACTTTGT | 10277 |
rs778931700 | in-del | -/A | 1.65497e-05 | 0.00287656 | intron-variant | UBE4B | GRCh38.p7 | 1:10117409 | AATGCAAACTCTGCC[-/A]AAAATAATCAAGAGA | 10277 |
rs778965719 | snp | C/T | 3.31164e-05 | 0.00406904 | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171340 | ACCAGGTCAGTGAGT[C/T]GAGTTGGTCTCTCTG | 10277 |
rs778992472 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146575 | AGTGGCCAGCATTTT[A/G]CCCGAGGGCAGCTCG | 10277 |
rs779005065 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135692 | AGTGAGCCATGATCA[C/T]GGCACTGCACTCCAG | 10277 |
rs779021583 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106854 | AACCCTTTTTGGCCT[A/T]TTGTCCTGTTGCCAG | 10277 |
rs779047636 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134918 | CCAGCCTGGGCAACA[G/T]AGTGAGACCCCATCT | 10277 |
rs779051864 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10116406 | CCTTGGTGTACGAAA[A/G]TGCTGGGATTACAGG | 10277 |
rs779066592 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040676 | AGGCTGGAGTGCAAT[A/G]GCGCGATCTCAGCTC | 10277 |
rs779069387 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058411 | AAGCCTTGGTACTTT[A/G]CTTGTTAGTGCAGAC | 10277 |
rs779069469 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072678 | CCTGATAGGATGTTT[A/G]GAACTATCTCATTAA | 10277 |
rs779107298 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045916 | TTGTAACAGAGAGAC[A/G]TGAAGTGGCAGCTGC | 10277 |
rs779110644 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181179 | TTCCCTCCACAGACA[A/G]TGTCCTCTGTTCAAT | 10277 |
rs779120926 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059630 | ATAAAGCCATGGAAG[C/T]GTGGCTGCTTAGGGC | 10277 |
rs779124753 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147077 | CTCCGCATCCTGGAC[C/T]CCGCATATCCCGAGT | 10277 |
rs779131307 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145730 | ATGCATTTCCATGAT[A/G]TTTGACAAAGAGTAT | 10277 |
rs779148298 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117041 | GTAGAAGTCACAAAG[A/G]TGAGGGCTATTTTGT | 10277 |
rs779157060 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10094713 | TGGTGGGATTACAGG[C/T]GTGAGCCACCACACC | 10277 |
rs779183499 | snp | C/G | 1.6582e-05 | 0.00287936 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106277 | CTCTTGCCTCACCTT[C/G]CCGTGCAGCCAGCCA | 10277 |
rs779187062 | snp | C/T | 1.65029e-05 | 0.00287248 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135035 | TATGCTGAATTTCCT[C/T]TGGGTACTGCAGCAG | 10277 |
rs779198742 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129941 | ACAGGCGTGAGCCAC[C/T]GCACCGGGCCTGTTT | 10277 |
rs779205431 | snp | A/G | 1.79216e-05 | 0.00299341 | intron-variant | UBE4B | GRCh38.p7 | 1:10101247 | AAATAAACACATTTC[A/G]TGTCTTGTATCTGTA | 10277 |
rs779212741 | snp | C/T | 1.66846e-05 | 0.00288826 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178678 | TGTTTGAAGAAGTTA[C/T]TTCAAAGATGCGGAA | 10277 |
rs779237984 | snp | A/G | 1.65877e-05 | 0.00287986 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151545 | GTTGGTACCTTCCCT[A/G]ATGAAGTTTTATACA | 10277 |
rs779239954 | snp | A/G/T | 3.30405e-05 | 0.0040644 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179531 | GGACCCCTTCAACCG[A/G/T]CAGACGCTGACAGAG | 10277 |
rs779251143 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160716 | TTTTGAGGGGCTGAG[A/G]TGGGAGGAACGCTTG | 10277 |
rs779260062 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058085 | GGCCAGGAGCCGACA[C/T]GGATGATCCCCTTCT | 10277 |
rs779293010 | snp | A/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158455 | GGCAAAACATAGCTC[A/T]CCATGGCACCTTTAT | 10277 |
rs779299142 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071150 | GACCTCGTGATCCTC[C/T]TGCCTCAGCCTCCCA | 10277 |
rs779323328 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10157867 | AACAAGTTTGATTTT[C/T]ATCCCTCTTTAATAG | 10277 |
rs779328294 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160326 | GTTTTCTTATCTGTT[A/G]TATGTGGTTAATTAT | 10277 |
rs779335283 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10085845 | CCCAGGCTGGAGTAC[A/G]GTGGCGCGATTTTGC | 10277 |
rs779361794 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087908 | TTGTCCCTTCTCCCC[-/T]GCTATGTATTTAATC | 10277 |
rs779364623 | snp | G/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031047 | CCACTGATGTGAAAT[G/T]TCCAGAATAGGCAAA | 10277 |
rs779373122 | snp | A/C | 1.69481e-05 | 0.00291098 | intron-variant | UBE4B | GRCh38.p7 | 1:10103135 | GCAGAGTACTCGACA[A/C]GAAAATAAGATGTGA | 10277 |
rs779377791 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159548 | CATGGTGGTGGGCGC[A/G]GTGGCGGGCGCCTGT | 10277 |
rs779420344 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098796 | AACTACAGCAACTCT[A/C]CTATTCAGTGGTGAG | 10277 |
rs779420529 | in-del | -/G | 1.66084e-05 | 0.00288165 | intron-variant | UBE4B | GRCh38.p7 | 1:10158306 | GCAATAACTGGATTT[-/G]GAAAGCAAGAAAATA | 10277 |
rs779435298 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10128724 | CTCTTCGGCTCATGT[A/G]GCAACTTCTAGAGCT | 10277 |
rs779437573 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040115 | TTTTGGAGAAAGCAC[-/AT]GTTTCTTTTTTTTTT | 10277 |
rs779451135 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086042 | AGTGGCACAATCTCC[A/G]CTTACTGCAAGCTCC | 10277 |
rs779472115 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10119576 | CAGTGCATATCCCAT[A/T]CTGCTTTAGTACTAC | 10277 |
rs779482098 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172910 | GTTTAGAATACTCAC[C/G]ATTGTGTTACAACTG | 10277 |
rs779483619 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172694 | AATAGAAGCATTGTA[G/T]GTACTTTTTTTTAAT | 10277 |
rs779485676 | snp | C/G | 1.91786e-05 | 0.0030966 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135176 | TGTGAATGACTGGCT[C/G]ACTGAACTCTGTGAG | 10277 |
rs779489055 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038818 | TTTGGGAGTTGGGGC[C/T]GGGCGCGGTGGCTCA | 10277 |
rs779513612 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102678 | GGCCTTCCAGAATGC[C/T]GGGATTACAGGTGTG | 10277 |
rs779523673 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049470 | AACACTGTAGCCAGA[C/T]GCAATGATGCATGCC | 10277 |
rs779558409 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10172004 | CTTGACAAATCCATT[A/G]CATTTCTGAAAAGAG | 10277 |
rs779560572 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060289 | AGTATAACTCCTTGG[A/G]TACTTACGGTATGGC | 10277 |
rs779577126 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051264 | ACTTATAAAATGGGG[A/G]TATGGAATACCATCT | 10277 |
rs779598640 | snp | A/C/G | 0.000218224 | 0.0104436 | intron-variant | UBE4B | GRCh38.p7 | 1:10144904 | AAGATGGATCCGGCT[A/C/G]TTTTCTTTCATTTGA | 10277 |
rs779619174 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10153439 | AGGCTGCAGTGAGCT[A/G]TGATCTTGCTGCTGC | 10277 |
rs779639957 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064067 | CTTTCTTGTCTGTGC[C/T]TCACCATGTCCATAC | 10277 |
rs779643143 | in-del | -/TTTA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103404 | ATTACCTCCTCTTTA[-/TTTA]TTTATTTATTTATTT | 10277 |
rs779662476 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10121471 | GCTGGAGTGCTCACT[A/G]TAACCTCAAACTCCT | 10277 |
rs779674134 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10105588 | CCACTCAGACCAGAG[A/G]TGAAAACCCATTTGC | 10277 |
rs779675897 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10098863 | ACAAGGATGACTGCT[A/G]TTTCTTCTTGTATTT | 10277 |
rs779753357 | snp | A/G | 3.30267e-05 | 0.00406353 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10168179 | TTGCTCAGGATGAGC[A/G]TGTGTCCCGCTCTTA | 10277 |
rs779795147 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103277 | TCCACTGATCTTATC[A/G]ATAACTTATTTTTCA | 10277 |
rs779799059 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10129942 | CAGGCGTGAGCCACC[A/G]CACCGGGCCTGTTTT | 10277 |
rs779820380 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130734 | AAGTGGTTGAAAAAT[A/G]CTTCTCAGGGCCTGC | 10277 |
rs779821218 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10057370 | TTGGAGAATTAAAGG[A/G]TCGCAACCTTTTTTT | 10277 |
rs779824174 | snp | G/T | 6.68863e-05 | 0.00578262 | intron-variant | UBE4B | GRCh38.p7 | 1:10149162 | TTCATTTAATAAATT[G/T]TCCTTTTTTTCTCTT | 10277 |
rs779885349 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146399 | AGAGGTTGCAGTGAG[C/T]CAAGATCGCGCCACT | 10277 |
rs779887336 | snp | C/T | 8.27849e-05 | 0.00643316 | intron-variant | UBE4B | GRCh38.p7 | 1:10119480 | TTGTATTGTTTGTTT[C/T]TTGTCGTCCTCACTT | 10277 |
rs779895394 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133451 | ACTCAACCAATATTA[A/G]CTATCATTCTTATCA | 10277 |
rs779906564 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110861 | TTCTGGCTGGGCACA[A/G]TGGCAAGCACAGGTA | 10277 |
rs779961371 | in-del | -/ATCTCAAAAAAAAAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10092824 | TAAGAGTGAAACTCT[-/ATCTCAAAAAAAAAAA]AGAAGAAAGAAAAGA | 10277 |
rs779980732 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090232 | TCAGGTGACCCACCC[C/G]CCTCAGCTTCCTGAG | 10277 |
rs779997798 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126677 | TTATATGCAAAAAAG[C/G]TTTTCCCTGGGGAAG | 10277 |
rs780051391 | snp | A/G | 1.70165e-05 | 0.00291684 | intron-variant, missense | UBE4B | GRCh38.p7 | 1:10101223 | TGAAGCCCTTGGTAC[A/G]GGTAATAGAAATAAA | 10277 |
rs780062085 | snp | C/G | 1.65274e-05 | 0.00287462 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095426 | TTGAACATTATTTCA[C/G]ATGGGGCTTCATCCT | 10277 |
rs780064140 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044131 | GCAACCTCCACCTGC[C/T]AGGTGCCAGGTTCAA | 10277 |
rs780070771 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170733 | TATGGGGAAAAAAGT[G/T]TATGAAATACTGGCT | 10277 |
rs780088491 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10061275 | TTGTTTGTTTTTTTG[C/T]GAGACAGAGTCCCTG | 10277 |
rs780092950 | snp | C/T | 1.66488e-05 | 0.00288515 | intron-variant | UBE4B | GRCh38.p7 | 1:10179882 | ATTAATCCTCCTTTT[C/T]TTCTTTTCTCAGTGC | 10277 |
rs780103311 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10056669 | AAATCGAGGCTCAGA[C/G]AGATAACCCAGCTGG | 10277 |
rs780128618 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10045075 | GCAATGTAGATCCCT[C/T]GCGTGCAGAACTCAA | 10277 |
rs780129047 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124999 | GGCGCAGAAGTGCAT[A/G]CCTGTAGTCCCAGCT | 10277 |
rs780129887 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10178021 | CCACAACTTCCCTTC[C/T]TGGGGACATAAATCG | 10277 |
rs780148278 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179222 | AGTAGCTGACAAAGA[A/G]GCGCCTTCCCCTTAC | 10277 |
rs780158455 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043221 | ACCATGTTGACCAGG[C/T]TGGTCTTGAACTCCT | 10277 |
rs780161718 | snp | A/C | | | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179431 | ACCCTCTGATGGACA[A/C]CCTCATGACAGACCC | 10277 |
rs780168290 | snp | A/G | 1.76166e-05 | 0.00296783 | splice-acceptor-variant, intron-variant | UBE4B | GRCh38.p7 | 1:10106196 | TTCTCAACTAATTTA[A/G]CCTCTATGAAAGTAG | 10277 |
rs780175715 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10095690 | TAGTCAGAAATGCCA[A/G]CTAGAGACCCATGCC | 10277 |
rs780184188 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10113397 | TGTGAGATTTGGACA[A/G]ACATCCCAACCATAT | 10277 |
rs780211708 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046019 | TGCGCTCATTAGGAG[A/C]CCAGGTGCCTTCTGT | 10277 |
rs780224557 | in-del | -/T | 8.40188e-05 | 0.00648092 | intron-variant | UBE4B | GRCh38.p7 | 1:10122092 | GTACGGTCGTATGAG[-/T]TTGCTCTTGCAAATT | 10277 |
rs780260340 | snp | A/G | 1.71384e-05 | 0.00292727 | intron-variant, downstream-variant-500B, missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171106 | ACTTGTCTCAACAGC[A/G]TGAATTGTCCTATTA | 10277 |
rs780270241 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10046612 | CTGGCAACCTTGATT[A/C]TGGTCTCTTGAAGGA | 10277 |
rs780281209 | snp | C/T | 3.30781e-05 | 0.00406669 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135000 | CAGACAGATGATAGA[C/T]TGGTGTCTACAGATG | 10277 |
rs780316678 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107083 | GTGTTTCTATAATTT[A/C]GGTGAATTATGTTTC | 10277 |
rs780322492 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074886 | TTCCTAAGCTTTTAT[C/G]TCCAACGTGGACCTG | 10277 |
rs780328199 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082372 | CAGGCATGGTAGTGC[A/G]CACCTGTAGGCCCAG | 10277 |
rs780330455 | snp | A/G | 6.79209e-05 | 0.00582717 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10135139 | CCAATGATGAGACGC[A/G]TGTGAATGCAACGAT | 10277 |
rs780332508 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10121990 | CCGTCCTTCCTAGTG[C/T]CGTATATGCTGTGTA | 10277 |
rs780357308 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10071504 | GAGGTGGGAAGATTA[C/T]TTGAGCCCAGGAGTT | 10277 |
rs780370690 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117971 | GGACTGTGCCAGGTC[A/G]ACATTAGCTTGTATC | 10277 |
rs780377609 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110160 | GAATCATCAGGGGTT[A/G]GATCGCTCTCTCCAT | 10277 |
rs780382664 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162822 | AGTGTCTGTTATTCC[C/T]GTCTCCGTCCATGTG | 10277 |
rs780387373 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093117 | TACAGTTTTTAAAAC[-/A]AATTTGTAATTATGT | 10277 |
rs780387840 | snp | C/T | 1.67122e-05 | 0.00289064 | intron-variant | UBE4B | GRCh38.p7 | 1:10151318 | TTGCTCTTCTTGCCT[C/T]TGTTCAGATACTCTC | 10277 |
rs780398340 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10038939 | ATGGTACGCACCTGT[A/G]ATCCCAGCTACTCAG | 10277 |
rs780427995 | in-del | -/TT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10074346 | CCATCTCATATGGCC[-/TT]TTTTTTTTTAACAGC | 10277 |
rs780451731 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10072899 | GTAAAGGGGGTGCTA[A/G]GAGAACTGCATTGAT | 10277 |
rs780456251 | snp | C/T | 3.56716e-05 | 0.00422309 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106547 | CCTCACCCAGTGCCA[C/T]GAGCAGACGCCCCTC | 10277 |
rs780459195 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137580 | GAAAAAGTAACCATG[A/G]TTTCCCTTGATAACC | 10277 |
rs780477381 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090899 | TTTGTACTTGAAAGG[A/G]AACATCATTCAGGAA | 10277 |
rs780497636 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10147499 | CTCTGTCCCCACCCA[A/G]AAAAAAAGATAATTC | 10277 |
rs780498856 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124951 | GGCAACATGGCAAAA[-/C]CCCATCTCTACTCAA | 10277 |
rs780504581 | snp | C/G | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10117533 | AAACCTGCAAAGAGA[C/G]AGATATGCTGAACTA | 10277 |
rs780505360 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156197 | TAAGAAGAAAAAAAA[-/A]CTGTTGGGAGAAATG | 10277 |
rs780507681 | snp | C/T | 1.88156e-05 | 0.00306715 | intron-variant | UBE4B | GRCh38.p7 | 1:10106616 | GAGTTGCATGTGTGT[C/T]TGCGGTGCAGGGAAA | 10277 |
rs780557063 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10054724 | CCATGGTAACACTTG[-/C]GGGGCATTTTTTTTG | 10277 |
rs780561984 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100710 | CAGGCATGTGCCACC[A/G]CGCCTGACTAATTTT | 10277 |
rs780576161 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10118081 | TCAGAGAGATTAAGT[A/G]CTTGTCCAGAATCAC | 10277 |
rs780591036 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075084 | ACCTGGATTGGCAAA[-/CT]CTTTCTGTTAAGGGC | 10277 |
rs780601729 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10130750 | CTTCTCAGGGCCTGC[C/T]ATTACCCTGGAAAAC | 10277 |
rs780601809 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10117122 | GTCTGGCTTTAACCT[A/G]CAGCCCTCTGAGTGA | 10277 |
rs780609285 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174121 | AGTGTTGGGGCTGGG[C/T]GCAGTGGCTGACACC | 10277 |
rs780634220 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175702 | AAAAAAAATAAAAAT[C/G]CCATCAGTCACACTT | 10277 |
rs780635862 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10040393 | GGATTACAGGTGTCA[A/G]CTACCACGCCAGGCC | 10277 |
rs780638680 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086717 | CTCTTTTTTTTTTGA[A/G]ATGTAGTCTCACTGT | 10277 |
rs780652409 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10106909 | AAGCAGGTGTGGGAG[C/T]AAATCTGGGCCTGGT | 10277 |
rs780680366 | in-del | -/AT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134640 | GACAGTGGTGATGAG[-/AT]ATATGTCTTCTCATT | 10277 |
rs780699903 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058652 | CTGCATCCTGAGCCC[A/T]CCAGCTGCCGCCTGC | 10277 |
rs780704307 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090128 | TGTGTGTGTGTGTGT[-/G]TTTTTTTTTTAGGCA | 10277 |
rs780730405 | in-del | -/AAAA | 4.63006e-05 | 0.00481125 | intron-variant | UBE4B | GRCh38.p7 | 1:10117623 | GAAATGGATTAACTT[-/AAAA]AAAAAAAAGCCTAGT | 10277 |
rs780754663 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10171562 | AGCCGTGATTGCACC[A/C]CCACACTCCAGAATG | 10277 |
rs780787444 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051659 | TGTACTAAGAGGGTG[A/C]AGGTGGAGTGTAGAG | 10277 |
rs780802417 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10160381 | AGTATATGCGTTTTT[-/C]CTGTTCTAGTCTGGA | 10277 |
rs780813858 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | UBE4B | GRCh38.p7 | 1:10119469 | ACAGCATGGAATTGT[A/G]TTGTTTGTTTCTTGT | 10277 |
rs780829762 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111186 | CATGGTCTACAAGGC[C/G]CTGCATCTCACGTAC | 10277 |
rs780833629 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10079524 | ATAGGAATATAATTA[C/T]CAACATATTTTTAAA | 10277 |
rs780838093 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10100090 | TGCCTCCCGGGTTCA[C/G]GCCATTCTCCCGCCT | 10277 |
rs780845235 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10086905 | ATGTTGGCCAGGCTG[G/T]TGTCAAACTCCTGAT | 10277 |
rs780856519 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10161200 | GACACGACGTTTTTG[C/G]TCGATGAAAGTCTGG | 10277 |
rs780857332 | in-del | -/G | 1.64985e-05 | 0.0028721 | intron-variant | UBE4B | GRCh38.p7 | 1:10147141 | TGGCTGGGCTCTGTT[-/G]GTCTTTATTGTCCTT | 10277 |
rs780862213 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075602 | CTCTATGCTAAGTAG[C/T]CCTGATTATGTTTCT | 10277 |
rs780881504 | in-del | -/CT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10179749 | ACATCCAGTCCCTCC[-/CT]CTCATGTCCCAGTCC | 10277 |
rs780896562 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10087809 | CGAGTTCCTAAGTCC[A/C]TCCCACACTTAAGGG | 10277 |
rs780899441 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10039014 | GCAGTGAGCCGAGAT[G/T]GCGCCACTGTACTCT | 10277 |
rs780909483 | snp | A/T | 6.58946e-05 | 0.0057396 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137105 | GAGCCGAAATTCCCT[A/T]CGGAGTGCTTCTTTC | 10277 |
rs780923562 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093367 | CTGAAATTAATGAAT[A/C]AAAAGTTTTACTGTA | 10277 |
rs780940441 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10130135 | CTGGAGCGCAGTGGC[A/G]CAATCTCAGCTCACT | 10277 |
rs780947255 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10148524 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 10277 |
rs780953319 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171314 | TCGGTTCGCGAAAGC[C/T]ATTGCTGACGACCAG | 10277 |
rs780953413 | snp | C/T | 1.6609e-05 | 0.0028817 | intron-variant | UBE4B | GRCh38.p7 | 1:10146921 | CCTGTAGGGACTTAG[C/T]TACTGACTGATCTTT | 10277 |
rs780960595 | in-del | -/ATACA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136149 | AAAAATGGAGATTTT[-/ATACA]ATACATCAGTAAGGA | 10277 |
rs780968429 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072184 | AATGTCCACAACATG[A/T]CCCCAGCTACCTCCC | 10277 |
rs780981252 | snp | C/G | 1.66029e-05 | 0.00288117 | missense, intron-variant | UBE4B | GRCh38.p7 | 1:10106262 | CCGTGATGGGCCCGT[C/G]TCTTGCCTCACCTTC | 10277 |
rs780983694 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10152804 | TCCGTCTCAAAAAAG[-/A]AAAAAAAAAAAGCAC | 10277 |
rs780988992 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10180567 | TTTAATTGGTGTTAG[A/G]TGACATGATTAATAA | 10277 |
rs781005463 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167825 | CTCGATCTCGACCTC[A/G]TGATTCGCCCACCTT | 10277 |
rs781006256 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10147065 | ATTCAGCTGCTGCTC[C/T]GCATCCTGGACCCCG | 10277 |
rs781017734 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | UBE4B | GRCh38.p7 | 1:10130711 | TTTTTCCTTCTCTTT[A/C]CAGGTTAAAGTGGTT | 10277 |
rs781037314 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10102355 | ACATCCTCTGTCACA[C/T]ATTTTTCCTTGGTGA | 10277 |
rs781052763 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10043310 | CACCGCACCCGGCCA[A/C]CTTTCAGTAAAAACT | 10277 |
rs781073489 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112095 | TTAAAATGGGATTCA[C/G]TCTGCACAGATCGGA | 10277 |
rs781108056 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10072123 | GAACCCTCCGGGGCC[C/T]CCCATAGCGGCATCA | 10277 |
rs781114271 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078125 | AGTGATTCTCCCACC[C/T]CAGCCTCCGAGTAGC | 10277 |
rs781115765 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10068930 | GGATCTTTAAGATGG[C/G]GCAAAATGTATTCTC | 10277 |
rs781145515 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10058734 | ACACTGACCTGAGCC[-/T]TCTGGGAGGCACTGA | 10277 |
rs781174655 | in-del | -/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10119791 | TCCTTTCTTCCTCAT[-/C]TTCTAAAGTAGTACA | 10277 |
rs781176680 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10135610 | GTGTGGTGGCACGCA[C/T]CTGTAATCCCAGCTA | 10277 |
rs781180715 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143831 | TGCTTCGGAGGTCAG[C/T]CTGACAGCACAGCCT | 10277 |
rs781186399 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10165890 | ATCCTCCCTAACGGA[A/C]TCTAAGCTGCATGAG | 10277 |
rs781193669 | snp | A/G | 1.66421e-05 | 0.00288458 | intron-variant | UBE4B | GRCh38.p7 | 1:10095647 | TTTAGGGAAAGAGAA[A/G]GATCCATTCACTTTA | 10277 |
rs781199597 | snp | A/G | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031269 | TAATTTTTGTATTTT[A/G]TATTTCACCATCTTG | 10277 |
rs781211006 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10158298 | TTGTTGGGGCAATAA[C/T]TGGATTTGGAAAGCA | 10277 |
rs781232042 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10044344 | ACAGGTGGGAGCCAC[C/T]GCGCCTGGCCCAGTT | 10277 |
rs781269531 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10170774 | ACTCAAAACTTTTTT[C/T]GCTCAGATAATGGTA | 10277 |
rs781272283 | snp | C/T | 6.59207e-05 | 0.00574073 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095469 | TGTTTAGGAGTAGCC[C/T]ATCGAAGCCAGAGCA | 10277 |
rs781315795 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10084200 | GCCTAGCAAAGGCAC[A/G]GGGGCAAATACTGTG | 10277 |
rs781334196 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10093472 | AAATTTAGTTTCTTA[C/T]TTCCTTCATAAATCC | 10277 |
rs781337004 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10140825 | AAATCACATAAAGTA[A/G]ATCCACCTTAATTTT | 10277 |
rs781344087 | snp | G/T | 3.31131e-05 | 0.00406884 | intron-variant | UBE4B | GRCh38.p7 | 1:10179573 | ACCAGGTAGAGGAGG[G/T]TGCAGTTTGAGGTGC | 10277 |
rs781352359 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089336 | TATCAGGAAATTAGC[-/T]GCTAAGAAAATGTCA | 10277 |
rs781371038 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10069734 | GAGACAGGGTTTTGC[C/T]GTGTTGGCCAGGCTG | 10277 |
rs781372165 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10150009 | TAGTATAGGTCCCCA[G/T]TCACAGAATACAAAT | 10277 |
rs781404214 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10034876 | CAGGACTGCCCATTC[A/G]GCGTTACTTTGTTTT | 10277 |
rs781405643 | snp | G/T | 1.70883e-05 | 0.00292299 | intron-variant | UBE4B | GRCh38.p7 | 1:10151294 | AGCAGTTTCTCAGCG[G/T]TCTCTTTCTTGCTCT | 10277 |
rs781407095 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137175 | GCCGTCGCTATATCC[A/G]CAGACTCCGGGCTAT | 10277 |
rs781462828 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10151503 | GTTTTTTGAAATGAT[C/T]GAGAACCATCCTCTC | 10277 |
rs781491516 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10171791 | GAGGCTGAGGCAGGA[G/T]AATCGCTTGAACCCA | 10277 |
rs781502653 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10108823 | CGTAGATAAAATCCT[A/G]TTGCATGATTATAGT | 10277 |
rs781535145 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10110912 | GAGGTGGGAGGCTTG[C/T]CTGAGCCCACGAGTT | 10277 |
rs781535413 | snp | A/T | 1.65102e-05 | 0.00287312 | intron-variant | UBE4B | GRCh38.p7 | 1:10126900 | TTTGTTCTTTTTCTT[A/T]AACTCATTCAATAGA | 10277 |
rs781555694 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10096010 | TCCTGGCCTCAAGAG[A/T]TCTTCCTGCCTTGGC | 10277 |
rs781579515 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137691 | AGCCTCAAATTTCCA[A/G]TTCATTAGCACCATG | 10277 |
rs781588366 | snp | C/G | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10129434 | TTTGGGAAGACACAC[C/G]CTGTGTGCAATTTGG | 10277 |
rs781589589 | snp | A/G | 1.69355e-05 | 0.00290989 | intron-variant | UBE4B | GRCh38.p7 | 1:10134978 | TACTTTTTCTTTTCA[A/G]CTTTCACAGACAGAT | 10277 |
rs781631565 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10126942 | CAGATTATTTTGACA[C/T]ATACTTTTCTTTCAG | 10277 |
rs781689604 | snp | C/T | 5.02281e-05 | 0.00501114 | synonymous-codon, intron-variant | UBE4B | GRCh38.p7 | 1:10106479 | CCCCCAAGCAGTGCC[C/T]GCCAGCAGTTCCAGA | 10277 |
rs781697772 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10125465 | GAGCTGTATTGATAT[A/C]TCACAACACTCCACG | 10277 |
rs781703234 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10112785 | AAAATTCTTGTAAAT[C/T]AGTTTTTGACCATTG | 10277 |
rs781724601 | snp | A/G | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178785 | AACGCACGCGCAGAA[A/G]TCGACTACAGCGACG | 10277 |
rs781748138 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10080078 | CTCAGGCTCCCGGCT[A/G]TGCATTGTAGATTTT | 10277 |
rs796067966 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167653 | GCTGGAGTACAGTGG[C/T]GCGATCTCAGCTCAC | 10277 |
rs796091148 | multinucleotide-polymorphism | CCC/TCA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066063 | CTCCCCCACTCCTTC[CCC/TCA]CTCTCCCTCTCTACC | 10277 |
rs796092310 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10063910 | GAAACTGTCTCAATG[-/A]AAAAAAAAAAAAAAG | 10277 |
rs796131240 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10089037 | TTTGAGATAAAGTCT[C/T]GCTCTATGGCCCAGG | 10277 |
rs796133568 | in-del | -/AAAA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166971 | CACACACACACACAC[-/AAAA]AAAAAAAATTAGCTG | 10277 |
rs796170754 | in-del | -/TCTCTCTGTC | | | intron-variant | UBE4B | GRCh38.p7 | 1:10111000 | ACCCTGTCCCTCTCT[-/TCTCTCTGTC]TCTCTCTGTCTCTCT | 10277 |
rs796179632 | in-del | -/AA | | | intron-variant | UBE4B | GRCh38.p7 | 1:10166971 | CACACACACACACAC[-/AA]AAAAAAAAAATTAGC | 10277 |
rs796185804 | multinucleotide-polymorphism | AT/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10133211 | TTGACTAGTAATAAA[AT/TG]ATGAATGAATGATGT | 10277 |
rs796216860 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051541 | GGAATCCTCTCCCCC[A/G]ACCCATTAGTTCCAA | 10277 |
rs796220557 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10103632 | GTTTGTTTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 10277 |
rs796261949 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10159704 | AAATAAATAAATAAA[A/T]AAAAATTTTATCCCA | 10277 |
rs796268843 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156029 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 10277 |
rs796276438 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146234 | AGGCAGGCAGATCAC[C/G]TGAGGTCAGGAGTTC | 10277 |
rs796290353 | in-del | -/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066315 | GTGGGATTGGGGGGG[-/G]AGGGGGTCTTGCCAT | 10277 |
rs796307294 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176868 | TCAGCCTACTGCAAC[C/T]TCCACCTCCCAGATT | 10277 |
rs796324690 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10124599 | ATCTAGAGAGGAATG[A/G]TAACTGGGATGGAGC | 10277 |
rs796361295 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10104581 | AAAAAAAAGTCCTTT[G/T]TATTTCTGGAGGATA | 10277 |
rs796367160 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10146536 | AATTCTGTCAACAGG[A/C]CTCTAGGTAGGAATT | 10277 |
rs796396892 | snp | G/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10136148 | GAAAAATGGAGATTT[G/T]ATACAATACATCAGT | 10277 |
rs796401884 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10156239 | GTTTCATTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 10277 |
rs796440251 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10075366 | TCCACCGCTATTACC[A/C]AGGTCCAAGGCACCA | 10277 |
rs796447474 | in-del | -/TCAGCAT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162949 | GTTTGTCTTCGCCAA[-/TCAGCAT]AGCTGAAAATTCTCA | 10277 |
rs796454614 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10154115 | GGACATGGTGGCATG[C/T]GCCTGTAGTCCCAGC | 10277 |
rs796474157 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181236 | GACACACGTTCAGAA[G/T]AAATCTTCTTTGAGT | 10277 |
rs796511292 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10060199 | ACGTTCTGAGAAACG[C/T]ATCATTATGTGAACA | 10277 |
rs796543459 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10051827 | AAGAATTGTACCCCT[A/C]CCAGCAGGGGGAGAA | 10277 |
rs796567693 | snp | A/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088853 | CCAACTAATTTTTTT[A/T]TTATTTGTAGAGATG | 10277 |
rs796592047 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10078343 | TTAAAATGTAGGGCT[C/T]ACTGCAGGTCAGACA | 10277 |
rs796602930 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10107594 | TTTTTTTTTTTTTTT[-/T]GAGGCAGAGTTCTGC | 10277 |
rs796622897 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10163050 | TATTTTATTTACTTA[C/T]TTGTTTTTTATTATT | 10277 |
rs796635330 | snp | G/T | | | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032060 | ATCTGGCTGATTTTT[G/T]GTATTTTTTAGTAGA | 10277 |
rs796645952 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10064420 | TATTTCTATGCATAC[A/G]TGCAGTAAGTAATAG | 10277 |
rs796660720 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10059210 | ATTCCAGCCCTGGGG[C/G]ACAGAGCGAGACTCC | 10277 |
rs796663232 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10175433 | AGGCGGGCGGATCAC[CA/TG]GGTCAGGAGATCGAG | 10277 |
rs796674240 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10099883 | TGATCTTTCCAGTAA[A/G]TGGTGCTAGGGCAAT | 10277 |
rs796702319 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10167073 | GGAGGCGGAGGTTAC[A/G]GTGAGCCGAGATTGT | 10277 |
rs796717877 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10162895 | GTATTAAAGTTCTAC[C/T]CATTCTCTGAGTAAG | 10277 |
rs796719704 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173928 | ACATTGCATTGCCTG[A/G]TCATGCCTTAGATTA | 10277 |
rs796767246 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10088793 | AAGTGATCCTCCTAC[C/G]TCAGCCTCCTGAGTA | 10277 |
rs796788183 | in-del | -/GT | | | intron-variant | UBE4B | GRCh38.p7 | 1:10101977 | TGCTCTGCATTTAGG[-/GT]GTGTGTGTGTGTGTG | 10277 |
rs796807952 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10134217 | ATGGTTCAGTAAAAG[A/C]ATGTATAAAATGGCC | 10277 |
rs796823190 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10176778 | AAGAGTTCTTTTTTT[C/T]TTTTTCTTTTTTTTT | 10277 |
rs796846118 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10144394 | ATATTCACCAAATCT[C/G]TAGTGCCATCCATTC | 10277 |
rs796950340 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10143091 | CCAGGGCAACAGAGT[A/G]AGAGACCCTGTCTCA | 10277 |
rs796962282 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10095538 | AGCCTTGAAACGCAA[G/T]CTCAGTCTCTCTCAC | 10277 |
rs796969203 | in-del | -/A | | | intron-variant | UBE4B | GRCh38.p7 | 1:10174392 | GCAAGACTCCATATC[-/A]AAAAAAAAAAAAAAG | 10277 |
rs796999757 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10055510 | TTTTGTAGCGATGGG[C/G]TCTCGTTATGTTGCC | 10277 |
rs797010785 | in-del | -/TG | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090794 | AGAAGCCTATGCATT[-/TG]TGTGTGTGTGTGTGT | 10277 |
rs797014546 | snp | C/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10145659 | GCCTTATGCAGGGCC[C/T]TCCTCACCTGCTGTC | 10277 |