SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs112141237 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169415 | GAGTCTCACTCTGTT[C/G]CCCAGGCCAGAGTGC | 9690 |
rs112156551 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157153267 | GTGAGCAGACGCTAG[A/G]TTGTTGGCAGTTAGT | 9690 |
rs112163639 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | UBE3C | GRCh38.p7 | 7:157156285 | CTTTCACCTCCACTC[C/G]TCACACCCCCAGTTC | 9690 |
rs112166009 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157222681 | TCTCGCCTCAGCCTG[C/G]GATTACAGGCATAAG | 9690 |
rs112169922 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157203446 | TCTGACTACGCCAGC[C/T]TTGGTTTTCATTAGT | 9690 |
rs112194007 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | UBE3C | GRCh38.p7 | 7:157237242 | GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAC | 9690 |
rs112256973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220965 | GGCCACCTCTTCAGC[A/T]GCCACCCATTTCTGT | 9690 |
rs112275774 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157241253 | CTTAGCTGTGAGACC[A/G]GGAGCACAAAAAACA | 9690 |
rs112277761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239653 | GAAAACTTGAGCAGC[C/T]GCTTAAGGGATATGG | 9690 |
rs112301421 | in-del | -/AAAC | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157153823 | TATACTAAAAATACA[-/AAAC]AAACAAACAAACAAA | 9690 |
rs112332230 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157225791 | CTGCCTCAACAACAA[A/C]AAAAGTGAGCTTATC | 9690 |
rs112334423 | in-del | -/TTA | 0 | 0 | cds-indel, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269201 | TGAATGTTCTATATC[-/TTA]TTAGTTAATTTGTAT | 9690 |
rs112338062 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264431 | CACACACACCTGGTA[C/T]TACAGGTGTGAGCCA | 9690 |
rs112340031 | snp | C/G | 0.15665 | 0.231917 | intron-variant | UBE3C | GRCh38.p7 | 7:157247578 | ATGCCTGTAATCCCA[C/G]CTACTGGGGAGGCTG | 9690 |
rs112350091 | snp | C/T | 0.5 | 0 | stop-gained, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267702 | GACGAGACACTTTTG[C/T]GAAGTAAACTTCTCT | 9690 |
rs112366130 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | UBE3C | GRCh38.p7 | 7:157236951 | TGGCCAAGCTGGTCT[C/T]GAAATCCTGACCTCA | 9690 |
rs112378758 | snp | C/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157219417 | GGCCTCTCAGTGATC[C/G]AGCATCCCACACCAC | 9690 |
rs112411781 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157140833 | GGGAAGATAGCACGA[A/G]CTGTGTAAAAGAATC | 9690 |
rs112427696 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157207117 | TAGGGCCTTAGTCTG[A/G]GAACGACTGGCTTAC | 9690 |
rs112446821 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157168946 | GAATTTTATGGTATG[C/T]GAATTACATAGCTGT | 9690 |
rs112447085 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE3C | GRCh38.p7 | 7:157217396 | GCCTGAAGTGATCTT[C/T]CTACCTTGGCCTCCC | 9690 |
rs112458138 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157193446 | TTGTGTGGGAGCCAG[A/T]GTCTTCCATTGTGTT | 9690 |
rs112464723 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157193285 | TTTTAAAAAGAAAAA[G/T]TTCAGAAGAACAAAT | 9690 |
rs112589460 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264870 | AGCCACTGCTCCTGG[C/T]CACGTAATTTTTAAA | 9690 |
rs112593328 | snp | A/G | 0.155656 | 0.231515 | intron-variant | UBE3C | GRCh38.p7 | 7:157166517 | AGGCCGAGGCAGGCC[A/G]ATCACCTGAGGTTGG | 9690 |
rs112604958 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157156890 | ATTTTCAGCAGCCAA[A/C]AAAATAAAGCTGACT | 9690 |
rs112612291 | snp | A/G | 0.143959 | 0.226396 | intron-variant | UBE3C | GRCh38.p7 | 7:157237037 | ACACCCGGCAAGACA[A/G]TTTTCTATGTAAGTT | 9690 |
rs112643901 | snp | C/T | 0.140919 | 0.224948 | intron-variant | UBE3C | GRCh38.p7 | 7:157165500 | CCTTCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9690 |
rs112655728 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157142854 | AAAATAAAAGTTGAA[-/T]TTTTTTTTTTTTTTT | 9690 |
rs112662660 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157142007 | TTCCCCGTGTCGCAC[A/G]CCCACAGCATCTGAA | 9690 |
rs112706506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157199902 | TTCCAATATTATTAA[A/G]TATTTATTATTAAGT | 9690 |
rs112716943 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157186747 | TTTCTTTGCCCGAAG[A/C]AAAATGTGATTTCGT | 9690 |
rs112745032 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157226887 | GTGTTTTCAGAGTAT[C/T]TGGTGTGAATGAGAT | 9690 |
rs112760629 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137362 | CTTGTCTCAGCCTCC[C/G]AAGCAGCTAGAAGTT | 9690 |
rs112765769 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178762 | TGAAGTATTTTCGTC[C/T]GAGAATACTTACTTG | 9690 |
rs112781000 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157221065 | TCCTTTTGGTCAGCA[C/T]GCTGCATTTGAGGGT | 9690 |
rs112790066 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157190924 | CCCCTTTCCTTTTGC[A/G]TATGCCAGTCTCTTC | 9690 |
rs112803654 | snp | A/G | 0.067446 | 0.170804 | intron-variant | UBE3C | GRCh38.p7 | 7:157241399 | ATGATAAAAATGGGC[A/G]AAGGATCCAATTGGA | 9690 |
rs112819804 | in-del | -/T | 0.431473 | 0.171952 | intron-variant | UBE3C | GRCh38.p7 | 7:157261448 | GAGACGGTCTTACTG[-/T]TTTTTTTATTTTTCT | 9690 |
rs112839656 | snp | C/T | 6.59772e-05 | 0.00574319 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267689 | CCCCGAGTTCTATGA[C/T]GAGACACTTTTGCGA | 9690 |
rs112873548 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157172071 | TCTTGCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 9690 |
rs112899057 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230532 | AAACCCCATCTCTAC[C/T]AAAAATAGAAAAATT | 9690 |
rs112902099 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157201350 | AAAGAAAAGTATAAG[C/T]AGTAATAACAATAGT | 9690 |
rs112911954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157259818 | AAAATCATTGGATTG[C/T]ACATTTAAAGGGATA | 9690 |
rs112931120 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137030 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 9690 |
rs112945357 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157218887 | CTAACAAAACCCTTC[A/G]TCATCATATTTGTAG | 9690 |
rs112952641 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157168462 | TCAAGAGAAATGAAA[A/T]CCTGTATCCACAACA | 9690 |
rs112977304 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157238250 | TCACGCTCTGGAGTA[A/C]GACAGGCCAGTGGGG | 9690 |
rs112977337 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157260617 | CATTAACATTTATTA[C/T]GATAGACAAGGCTTC | 9690 |
rs113036889 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157201983 | CAGTGTCTAATCTTA[A/G]CAGTTACTTATCTGT | 9690 |
rs113051045 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157223775 | GAATACAAAAGTTAG[C/T]TGGGCGTGGTGGCAT | 9690 |
rs113070668 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157165952 | CTTTTGATGCTTTTA[A/G]AATTCAGTCTTTATC | 9690 |
rs113072269 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157149722 | GTCTCATAAGACCAT[A/G]GAATAGCCTCAAAAG | 9690 |
rs113082160 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157249336 | TTTTTTTTTTTTGAG[A/G]TGGAGTTTCACTCTT | 9690 |
rs113095219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226139 | TGTTCTAAAAATCTC[A/G]ATGGTAGCCATTTAT | 9690 |
rs113187327 | snp | C/T | 1.65526e-05 | 0.00287681 | intron-variant | UBE3C | GRCh38.p7 | 7:157169020 | GATTCTGACCAATTG[C/T]TCCCTCACTCCTCCT | 9690 |
rs113196914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196935 | GATAGCGCCATTGCA[C/T]TCCAGGCTGGGCAAC | 9690 |
rs113254185 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157266317 | AGACTCCGTCTCAAA[A/T]AAATAAATAAATAAA | 9690 |
rs113255488 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157246810 | CCACCTGTTCTCCAC[A/T]CCCCCGGGGGTAATT | 9690 |
rs113268237 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157140916 | AGGTTCACAAACACT[A/G]AAGAGATCCTTGTGC | 9690 |
rs113332480 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157223916 | CAAAGCCAGAACCTA[C/T]CTCAAAGGGGGGAAG | 9690 |
rs113340483 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157156280 | AGAGCCTTTCACCTC[C/T]ACTCCTCACACCCCC | 9690 |
rs113348430 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157233102 | TGGATTTTTTTTTTT[-/T]CTAGACATTTCATAT | 9690 |
rs113377265 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157261382 | TACCCCAGTCAAGAC[C/T]CCGCACAATCATAAT | 9690 |
rs113395462 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157189549 | TACTGTTTCAGAGTT[A/T]CATTGACTGCATTTG | 9690 |
rs113443695 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157245049 | TATCTCAGTTGCATA[C/T]ATTATGGAAATTTAA | 9690 |
rs113472110 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157223198 | CTTAAGAATTGTCAG[C/T]GGGAATGCAGGGGAA | 9690 |
rs113474621 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157205707 | ATTCATTGATGAATC[C/T]GTTCAGCATAGTGCT | 9690 |
rs113474971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193151 | CCAGACGAAATACAC[A/C]TTAAAATTTTTATTA | 9690 |
rs113497054 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157141877 | TGAACGCACCGTGGC[A/T]GATTCTGTTTTCTTA | 9690 |
rs113535675 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157249477 | GCCACCACGCCCAGC[G/T]AATTTTTGTATTTTT | 9690 |
rs113545880 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157259202 | AGCGCTCAGTGGGAG[C/T]GGAGCCCCGCAGTCA | 9690 |
rs113559705 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157141298 | AGATGGAACACCACT[C/T]ACATCAAAGGAAGAC | 9690 |
rs113572049 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157175800 | CATATTTTTTCTAAC[-/TT]ATTTCTTTAATAAAC | 9690 |
rs113582520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219586 | ATGGGAAATTTTACA[G/T]GATGAAAGTTTCTTC | 9690 |
rs113591659 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253066 | ATAAATACTTTTTAA[A/T]AATTTTTTTATTTAA | 9690 |
rs113615538 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157200138 | TTGCTTTTAGCCTAC[A/G]TGACATTGGAAAGAT | 9690 |
rs113620886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144019 | GTGCTGCACAGACAC[A/G]GTGAGTCCACTGACT | 9690 |
rs113624164 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | UBE3C | GRCh38.p7 | 7:157183302 | CTTCTGACCAACCTG[A/C]AAAAATGGGGGTTCC | 9690 |
rs113639344 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157155950 | TAACTGCTACTAGGC[A/T]TCCTTACGGGTTCTA | 9690 |
rs113639813 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165492 | AACCTCCGCCTTCCA[G/T]GTTCAAGCGATTCTC | 9690 |
rs113695927 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157229919 | TGCAATGTTTTAATT[A/T]ATTTATTTTTTTTTT | 9690 |
rs113701926 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157161934 | AGTTAGCCAGGTGTG[A/G]TGGTATGCACCCGTA | 9690 |
rs113713153 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157196791 | CTGACCAACAAGGAG[A/C]AACCCCGTCTCTACT | 9690 |
rs113720588 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157156601 | ATGAGCACCGCATCC[A/G]GCCCCAATTCTTTAA | 9690 |
rs113720731 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157178188 | ATAGTTAACCTGCAG[C/T]TCTTCTCATAGTAAG | 9690 |
rs113753884 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157247785 | TCACTCATTGACACA[A/T]TGTCCATGGCTGCTT | 9690 |
rs113782960 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157256052 | TTTGAACTGCAGCAC[A/G]GTTCTTCAAAATAAG | 9690 |
rs113789063 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBE3C | GRCh38.p7 | 7:157147994 | GGACATCAATTTAGG[A/G]TGTTTTTGTGATGTC | 9690 |
rs113817534 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157154404 | CTTCCCACCATTATT[A/T]TCTCAGTATCCTCTC | 9690 |
rs113834085 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157225740 | GATTGCTTGTGCTCA[A/G]GAGTTAGAGGCCAGC | 9690 |
rs113843207 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157235198 | CTGTCTCAAATTAAA[A/G]AAAAGAAAAGAAAAG | 9690 |
rs113851266 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157257196 | GGTTATGATGTATAT[A/G]TTTTGGTGCTAGTTT | 9690 |
rs113872236 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157156092 | TTCTCCTGGTACCTT[-/A]TTTGCCCCTTTCCTC | 9690 |
rs113958387 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154007 | GTCTGGGGGGGGAAA[A/T]GTTAACTTTTTCTGT | 9690 |
rs113965987 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264509 | TGCGCCAACATGCTC[A/G]GCCTGTTACACACAC | 9690 |
rs113986369 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157219562 | GGTGCAATTAGCAAA[A/C]TCTAGATTATGGGAA | 9690 |
rs113993803 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157241040 | AGCCAGGGATTTTAG[C/T]GGGAGGGAAGGGAAG | 9690 |
rs114011332 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | UBE3C | GRCh38.p7 | 7:157255428 | TGTGTGTATCCATGC[G/T]TATGTATCTCTTATC | 9690 |
rs114059997 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBE3C | GRCh38.p7 | 7:157172152 | TTCTCCTACCTGAGC[A/G]CCCTGAGTAACTGGG | 9690 |
rs114099130 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157152455 | TGTGCCTGAAGAGCA[A/G]TGAGGGCCTAAAACC | 9690 |
rs114103383 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157204505 | AGGTAATCGAGGTAC[A/G]GATGGTTTGGGGGCC | 9690 |
rs114117715 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157263696 | TCTAGCAAGTATTAG[A/G]AACATTCACTTTGTG | 9690 |
rs114143829 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157227294 | TGGGTGAGGGGAGCT[C/G]CGAGGGCACGGGTGC | 9690 |
rs114174700 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157236469 | CTTTGGCGTGGTTTA[C/T]AATTTTTTATCGCGG | 9690 |
rs114177717 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | UBE3C | GRCh38.p7 | 7:157251089 | ACTAAAGAGCCTAAT[A/G]AGAAAAATTAAGAAA | 9690 |
rs114188662 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE3C | GRCh38.p7 | 7:157257180 | TTTTTAATTAAGTAC[C/T]GGTTATGATGTATAT | 9690 |
rs114206774 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157205936 | GCTCCTTACGGCCCC[A/G]CTAATTAGAACAAGT | 9690 |
rs114243773 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157157028 | TTAAAAACTCATGTC[C/T]GGCCCAGGCGGTAGG | 9690 |
rs114274124 | snp | C/T | 0.0134861 | 0.0810011 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269564 | TCCCAGGCCGGCGGC[C/T]GGTGTGCTCCTATCC | 9690 |
rs114304476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157143550 | CACATGGTTTCCTAG[C/T]TTAAGCGTCAAGAAA | 9690 |
rs114304619 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | UBE3C | GRCh38.p7 | 7:157189177 | AATATGCCGAGGAAG[C/G]TGGGGCTGGAGCAGA | 9690 |
rs114337887 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157205446 | TAACAGTACAAGTAC[A/C]AGGATTCTTGTCGGG | 9690 |
rs114408937 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157175802 | TATTTTTTCTAACTT[A/C]TTTCTTTAATAAACT | 9690 |
rs114430480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157263308 | GGCGCCTGTCCTAAC[A/G]CCACCTTCCCGGGCA | 9690 |
rs114467100 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157160849 | GGAAAAGAGTTTTCT[C/T]TTCCTTGTTTATTGA | 9690 |
rs114490742 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE3C | GRCh38.p7 | 7:157265843 | GAGAATTTTCACACT[A/G]TACCTTTAAATACCA | 9690 |
rs114494506 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | UBE3C | GRCh38.p7 | 7:157243601 | GTGTCCTCCTGCTGC[C/T]GTTCCTGCATGTGAG | 9690 |
rs114575451 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157227052 | CCCACTTGACCCTGG[A/G]GGTCTTTACAGCTTG | 9690 |
rs114603575 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBE3C | GRCh38.p7 | 7:157149847 | CATCTTATTCTTTGA[C/T]TGTGACCCCTGTTTT | 9690 |
rs114606105 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157229664 | GATGGGGGTCTCACT[C/T]TCAGCCAGGCTGGAG | 9690 |
rs114632624 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157259784 | TGTGGGGGTCGCTGC[A/G]GAACTCTGTAAATTT | 9690 |
rs114695412 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157225197 | TATTTTAAACTGGGC[A/G]AAGGAGCAGCTTTAG | 9690 |
rs114700087 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157155710 | TTGGTAAGACAAAAC[A/G]AAAAGAAAATCACCT | 9690 |
rs114741580 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE3C | GRCh38.p7 | 7:157156754 | AGAGCATATTAAACA[A/G]ATTGCTGTACTTCTC | 9690 |
rs114746855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203955 | AAAATATGTGCATTA[G/T]CCTACAGCTAGGCAA | 9690 |
rs114755897 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157262374 | AAGAGACCTACAAAG[A/G]TCAGTAATAAGAATC | 9690 |
rs114756426 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157210786 | GACCTGACTCCTTCA[A/T]CACCGACCATTTTCA | 9690 |
rs114813402 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157140881 | ACTCTTTTTATTGAG[A/G]TATAACTTAAGATAC | 9690 |
rs114864393 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | UBE3C | GRCh38.p7 | 7:157159079 | TTGTGAAGTCATGGG[C/T]GGTAACTACCAGCAC | 9690 |
rs114906110 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157203131 | TTCAAATCATCTGGA[A/C]AAAACAGTTCATACT | 9690 |
rs114919572 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157152658 | ATCAAGGCCTGGAGT[C/T]CAAATAATTTAGCAA | 9690 |
rs115023266 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157165360 | ATATTTTCACCTGAC[C/T]TAATTTCTGATTTAC | 9690 |
rs115029558 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157249191 | TCACCCTAGCCAATG[C/T]TAGCACATTTTCCTC | 9690 |
rs115046229 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157176208 | TCGAGGCTGCAGTGA[A/G]CTGTGATTGTGCTAC | 9690 |
rs115049391 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269224 | TAATTTGTATATTTT[A/G]TTAGTATTTTGGAAA | 9690 |
rs115116924 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157240416 | TGCTGAAATTTGAGA[A/C]TTACTGGACAATGGA | 9690 |
rs115137408 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | UBE3C | GRCh38.p7 | 7:157165358 | GGATATTTTCACCTG[A/T]CCTAATTTCTGATTT | 9690 |
rs115160101 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157172383 | GTTTATCTGTGTTAA[A/C]AATTTCAAATTGCAT | 9690 |
rs115193346 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157244828 | ACAGTTGAAAAATTC[A/G]TTACAGGTCTTTTCC | 9690 |
rs115294788 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157262761 | CTCTTACTAGTTTTA[C/T]CCTTAACATAAATTA | 9690 |
rs115307946 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157241112 | TCCCTTCTGTGCCCG[C/G]TGGTTCAAGGGTGCA | 9690 |
rs115321205 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157247736 | CTTGACATGTGAAAA[C/T]CACATGAAACCCAAA | 9690 |
rs115339892 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | UBE3C | GRCh38.p7 | 7:157252825 | GTTCATTTATTTTGG[C/G]CTTATTTTATATTTT | 9690 |
rs115343314 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157233070 | CCTCCCCCAGCCCTG[G/T]CCAACCACTAGTCTA | 9690 |
rs115360670 | snp | C/G | 0.0263992 | 0.111815 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138475 | CTAGCTGCTCCTTTC[C/G]CGCCTCACTCGAGTC | 9690 |
rs115366973 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157183618 | CCTCACCATAAGTCA[C/G]CTCAAGTATGATCAC | 9690 |
rs115384843 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | UBE3C | GRCh38.p7 | 7:157171243 | CAATCGGTGGTGTCT[C/G]AGCCACCTAAGTAGC | 9690 |
rs115391536 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157158780 | TTTTTTTTCTAGCTC[A/G]TCAATTAGAAGAAAT | 9690 |
rs115473644 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE3C | GRCh38.p7 | 7:157247921 | AGGGTCCAATAGCTG[C/T]GAGGCCTTGTTTGGA | 9690 |
rs115497925 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | UBE3C | GRCh38.p7 | 7:157231849 | AGTCAAAACGGACTA[A/G]GACAGTAAGTTACTG | 9690 |
rs115503011 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157261406 | TCATAATTGAGTTAT[A/G]CCGTGGAAAACACTT | 9690 |
rs115528542 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157143592 | ATTACCAGTTTTCAG[A/G]AGAGGAAAGTCTGAT | 9690 |
rs115542153 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | UBE3C | GRCh38.p7 | 7:157257561 | TCAACATGATGAAAC[C/T]CTGTCTTTGCTAAAA | 9690 |
rs115611849 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157180726 | CCTCCCACCCAGAGT[C/T]CCTATCAGAAGCGTA | 9690 |
rs115664366 | snp | A/G | 0.00294851 | 0.0382826 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163812 | TGTTTGGGTGTAGGA[A/G]GAAAAGGCTTCTCTT | 9690 |
rs115693941 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157229115 | GTGCGGTTGCTTTCC[C/T]CTGACTTCATGCAGC | 9690 |
rs115695192 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | UBE3C | GRCh38.p7 | 7:157144187 | CCTACAATCTGCCAC[A/G]CCGAAGACTGAGGCG | 9690 |
rs115697163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239851 | AGGTAGAGGAACACT[A/G]GGTGCAGCTGCATGA | 9690 |
rs115917241 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157152717 | TATCCGGATGCTGTA[C/T]GGCCTCTCCCTCGTG | 9690 |
rs115942355 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157204993 | GAGGTTAGGGATTGC[C/T]TCGGGTCTCACTGAT | 9690 |
rs115943567 | snp | C/T | 0.141596 | 0.225274 | intron-variant | UBE3C | GRCh38.p7 | 7:157166727 | CCTGGAGTGAAACTC[C/T]GTCTCAAAAAAAAAA | 9690 |
rs115945756 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157211906 | CAAACCACAGAGGCC[A/G]GTCCTGTGGAAGCAC | 9690 |
rs115947862 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157238806 | AAGGTTTAGAGTCCA[A/G]AGAGTAGAGAATTGA | 9690 |
rs115954306 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBE3C | GRCh38.p7 | 7:157217605 | ACTTGGGGAAGCCGA[C/T]GGGCAGATCACTTAA | 9690 |
rs115997873 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157258757 | GAGCCATCATGCCCG[A/G]CCCCCCAAGTATTTT | 9690 |
rs116010943 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157164036 | GCCGGTGTAGAAAGA[A/G]ATGGACTAAAAGGGC | 9690 |
rs116013141 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157234905 | GTATGAAAATCTTTA[C/T]AATGGGCCAGGCATG | 9690 |
rs116013775 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157184867 | TTTAAAAAATAAGAG[A/T]AGACAAAGAAAGGAA | 9690 |
rs116016053 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157209564 | GGATGTGGGTGTTAA[C/T]GGTAGCATATTTGTT | 9690 |
rs116043482 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157183480 | TTGAGTTTTATGGTG[C/T]TTCTTCTCCAGTGTC | 9690 |
rs116051096 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157213317 | TCTCAAGTCGTAACT[A/T]CCTATCAGAGTCATC | 9690 |
rs116075039 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBE3C | GRCh38.p7 | 7:157248887 | GGTGCTGGGGGTGGC[C/T]GTTCAGCAGCTTCCC | 9690 |
rs116137326 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157259499 | AACGAAATAATTCAC[A/C]GTACATGAACTGCTA | 9690 |
rs116190766 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | UBE3C | GRCh38.p7 | 7:157165357 | TGGATATTTTCACCT[C/G]ACCTAATTTCTGATT | 9690 |
rs116256646 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157223607 | TTATAATGAGGGTCT[A/G]ACGTCATTTTTCTCT | 9690 |
rs116275464 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBE3C | GRCh38.p7 | 7:157218164 | AAAAGAAACCATGTC[A/G]GCTGGGCGCGGTGGC | 9690 |
rs116316637 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UBE3C | GRCh38.p7 | 7:157196230 | CTATGCAACGCTGCC[A/G]ACAAACTGATGTTAA | 9690 |
rs116333688 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157144154 | GGGCCGAACACAGGC[C/T]GGATGCTGTGGCGCA | 9690 |
rs116341660 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157254650 | TGATCCACCCCCCTC[A/T]GCCTCCCCAAAGTGC | 9690 |
rs116350853 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157225754 | AGGAGTTAGAGGCCA[G/T]CCTGGGCAACATACT | 9690 |
rs116380899 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE3C | GRCh38.p7 | 7:157219959 | CTCACGCCTGTGACC[C/T]GGGCACTTTGGGATG | 9690 |
rs116399864 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE3C | GRCh38.p7 | 7:157158345 | AACCATGCACTCATA[C/T]TTTATTTTGAAACCG | 9690 |
rs116401173 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157166469 | TTGAGGGCTGGGCGC[A/G]ATGGCTCACGCCTGT | 9690 |
rs116413497 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157211849 | GCAGTATCACCACGT[A/G]GTGAAGGAGACATGC | 9690 |
rs116495431 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBE3C | GRCh38.p7 | 7:157239704 | AAAGATGGGAGAAAT[A/G]ACAGCATGTGTATTT | 9690 |
rs116504809 | snp | A/G | 0.000451985 | 0.0150262 | intron-variant | UBE3C | GRCh38.p7 | 7:157207674 | AAGATGGAAAAAGAA[A/G]CAATAGAAAACTGGA | 9690 |
rs116658395 | snp | C/T | 0.00199082 | 0.0314872 | intron-variant | UBE3C | GRCh38.p7 | 7:157253938 | ATTTTGAGATCCTTA[C/T]GTTTTGTATTCCCAG | 9690 |
rs116684305 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157180994 | GTCAGGACTACAGTG[A/G]AATGAAACCTACCAA | 9690 |
rs116832054 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UBE3C | GRCh38.p7 | 7:157228682 | CAGAGGTGGCGGGCA[C/T]GGCAGGGCAGCACTG | 9690 |
rs116874997 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | UBE3C | GRCh38.p7 | 7:157195052 | CCTTCTCTAGAGAAA[C/G]TGATGAAGGTATGGC | 9690 |
rs116921642 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157178135 | GTGTCTTGATTGGTG[C/T]GGCCTGCCCGACTGC | 9690 |
rs116938125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157187130 | TTTTCTGGTAGAGAT[C/T]GATGTAGGATATTCT | 9690 |
rs116988498 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157176586 | AGCCAAACCCATGTT[C/T]CTTTAACAACAAGAA | 9690 |
rs117094664 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | UBE3C | GRCh38.p7 | 7:157262477 | CAGGCTGGAGTACAA[A/T]GGCCCATCTCAGCTC | 9690 |
rs117161828 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | UBE3C | GRCh38.p7 | 7:157145320 | GTCAAGAGTTCGAGA[C/T]CAGCCTGGTCAACAT | 9690 |
rs117165702 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268394 | ATGATGGTTTGGAGA[C/T]ACTGTCTGTGGATGT | 9690 |
rs117166444 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | UBE3C | GRCh38.p7 | 7:157203095 | CCAGGCACAGTCAGC[A/C]CCTTTATGATGGGAC | 9690 |
rs117243611 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157248651 | TGTGTGTGGAAGTCC[A/G]TTTGTGTTACAGCGT | 9690 |
rs117302446 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157220177 | GGTCGCACCACTGCA[C/T]TCCAGCCTGGGTGAC | 9690 |
rs117347133 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157259308 | GTTGCATTTAATTGG[C/T]GTGCTCTTTAGTTTC | 9690 |
rs117354991 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE3C | GRCh38.p7 | 7:157186368 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTCA | 9690 |
rs117368491 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBE3C | GRCh38.p7 | 7:157175645 | TTAATTTTCTGGACA[C/T]TGTCTGTAATATTTG | 9690 |
rs117368856 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157183258 | ACCCACTTCAGAGGC[C/T]GATTACAAGTAGTAG | 9690 |
rs117396195 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157216802 | TCCTCGAGTGAATGT[A/G]TGGCTCACTGTGCAT | 9690 |
rs117411654 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157159835 | CCAAAAAAATAAATA[C/T]CATTTGCTTGCCTGA | 9690 |
rs117505963 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157219242 | CCTTACTCCAGAAAG[C/T]TGTGCGATGGGAAAA | 9690 |
rs117506586 | snp | C/T | 0.147321 | 0.227941 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157138980 | CGGCAGTTCCAGGTG[C/T]AAGCGCCGGGTTTGC | 9690 |
rs117531237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259611 | ACTGTGCTAAGTGAA[C/T]GAAGCAAGACACAAG | 9690 |
rs117620134 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157229878 | TTGGCTTCCCAAAGT[A/G]CTGGGATTACAGAAG | 9690 |
rs117661799 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157227369 | GCCAGAGTAGAATGC[A/G]TTTCTTACTTACCAG | 9690 |
rs117690635 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | UBE3C | GRCh38.p7 | 7:157153437 | TCTTTGTTGTATTGC[A/G]TAATGGGAGAGTCAC | 9690 |
rs117701681 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | UBE3C | GRCh38.p7 | 7:157255069 | AGATCTCAGTGAGCC[A/G]AGATCATGCCACTGC | 9690 |
rs117706819 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157216422 | AGATAAACATGTCAT[C/T]GGAGTTTGTTGTACG | 9690 |
rs117779612 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157266421 | AATTTTTCTTTTTTT[A/G]GCAATAACATCACAT | 9690 |
rs117781865 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157253401 | AAAAGTGTTCTTACT[C/G]ACTCTGTTTATATAC | 9690 |
rs117786188 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157244912 | AACAAGCGTGGTACA[A/G]CTGGCTGAGAAGGCC | 9690 |
rs117798337 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157159960 | GCAGCGTAGCGTCTC[A/G]TATTCTTTTGTTGTG | 9690 |
rs117850363 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | UBE3C | GRCh38.p7 | 7:157218318 | GGCACGGTGGTGTGC[A/G]CCTATAGTCCCAGCT | 9690 |
rs117866424 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157221306 | AATCCTGAGACATTT[A/G]GCAAGTTTATGTTTA | 9690 |
rs117867775 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | UBE3C | GRCh38.p7 | 7:157230266 | CCCCCCTTTTCAGCC[A/G]AATACAGCTTTTAAA | 9690 |
rs117950714 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157230190 | GCTGGGATTACAGAC[A/G]TGAGCCACTGCACCT | 9690 |
rs118000717 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157213202 | ACATAATGCTATTGT[A/G]TTTCAGAACTTAAAA | 9690 |
rs118014838 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157195877 | GAGTGGTGGCGGGGC[A/G]GGGGTTGCACTGTAG | 9690 |
rs118044655 | snp | A/C/G | 0.00958686 | 0.0685685 | intron-variant | UBE3C | GRCh38.p7 | 7:157256891 | CTTTGCATTTCATAA[A/C/G]GCATGTGTTCATTTT | 9690 |
rs118053785 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157246616 | TATCACAGCATCTCC[A/T]GCAGCACAGCTCATA | 9690 |
rs118126401 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157264593 | CACACAAACATATAT[A/G]TTTTTAAGACAGAGT | 9690 |
rs118167631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157141788 | CACTTGTCGTTTGTG[C/T]CCGGCTGCTTTGGCT | 9690 |
rs137913944 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157241829 | GACTATTACTGGGCC[A/G]TAAAAAGGGGTAAAG | 9690 |
rs137970582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214336 | AATCTGTAGAAAATA[C/T]ATGTTCTTATGAACA | 9690 |
rs137976602 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157147045 | TTGCCTCTCCATAAG[A/C]GTCAGTTTGTTGATA | 9690 |
rs137977548 | snp | A/G | 0.00014834 | 0.00861092 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174957 | TAAACACAGCTCTCT[A/G]TTTGTCAAGCAGTTG | 9690 |
rs137995730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182372 | AACACACATATGGGT[A/G]GCATTGGCAGATGAG | 9690 |
rs138027924 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157153747 | TCTGGGAGGCTAAGG[C/T]AGGCAGATGCCTTGA | 9690 |
rs138028545 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157224045 | ACAGGATCTCACTCT[A/G]TCACCTGGGCTAGAA | 9690 |
rs138035029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157211043 | ATGAGATAGGAAATC[C/T]TGTTTTGAGATGTCT | 9690 |
rs138039346 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157144716 | AGACTTTATTTTTTA[A/G]AGCAGTTTCAGGTTT | 9690 |
rs138095554 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157191215 | GATAAACAGCGGTGC[A/G]CCTCGAAGCGCAGTG | 9690 |
rs138097397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151498 | CTGACTTAAAATGCT[A/G]TTTTTCTAGATGTGC | 9690 |
rs138121126 | in-del | -/AATT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254400 | TTTAATTAATTTATT[-/AATT]TATTTTTTTTTTTTC | 9690 |
rs138148498 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157256107 | CCTGCATTCATCTTT[A/T]TAGTTACAGGGTGAT | 9690 |
rs138153460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187426 | GCATCTCACTCTGTT[G/T]CCCAGAGTGCAGTGG | 9690 |
rs138181272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233283 | TGTATGGATATACCA[C/T]ACTTTGGGGTTTGTT | 9690 |
rs138197528 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157220590 | AGAGGGCCCAGCCCA[C/T]GGTAGAGAAATGTCC | 9690 |
rs138201644 | in-del | -/TTTG | 0.0803491 | 0.183626 | intron-variant | UBE3C | GRCh38.p7 | 7:157248310 | TTGAGCATATGGCTC[-/TTTG]TTTGTAGAAGGCTTG | 9690 |
rs138233488 | in-del | -/ATTA | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157254397 | TATTTTAATTAATTT[-/ATTA]ATTTATTTTTTTTTT | 9690 |
rs138310304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166010 | CTTGGAGATCGTTGA[A/G]TCTGCTGTATGTAGG | 9690 |
rs138313684 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157142949 | TCAGCTCACCACAAA[C/G]CTCCACCTCCCGGGT | 9690 |
rs138346319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175983 | TTTAAAAATAAAGGA[A/T]TCATGCTTCACTCAA | 9690 |
rs138359890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157160893 | GTAAGTATTGAGTCC[A/G]TGATGCGTGTTTGTG | 9690 |
rs138404997 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157266820 | TACCTCACTAACCTC[A/G/T]ACCTCCTGGGCTCAA | 9690 |
rs138407607 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168477 | ACCTGTATCCACAAC[A/T]AAACTTATATATGAA | 9690 |
rs138416735 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157206159 | CTTGCAGGTGAGCCT[A/G]TTAGCTAAAAGTTCC | 9690 |
rs138418204 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158240 | AAATTCAAAGGAAAC[A/G]CAAATATAATGAAGC | 9690 |
rs138418294 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | UBE3C | GRCh38.p7 | 7:157201141 | CCAGCCTGGCCAACG[C/T]TGTGAAACCTCATCT | 9690 |
rs138422763 | snp | C/T | 0.000181203 | 0.00951675 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267623 | TCACAACGGAGGCTC[C/T]GACCTTGAGCGGCTC | 9690 |
rs138455874 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157209952 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT | 9690 |
rs138494437 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157205501 | CAAGACGCAGGAGTG[A/G]GCTCCAGCTGTCATA | 9690 |
rs138499835 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157245685 | ACTTTGGTTTACCTG[A/G]CAGAGGCCAGCCGCA | 9690 |
rs138545016 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157151081 | GTGGTGACTTTGGTC[A/C]TGGTGTATTTGTCCA | 9690 |
rs138585580 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157255170 | GGGCAAAAAAAACCA[A/G]ATGTTTAACATAGAA | 9690 |
rs138630916 | snp | C/T | 0.000247152 | 0.0111137 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178784 | ACTTACTTGCCTGTT[C/T]TACAAGATGCTAGCT | 9690 |
rs138705497 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157176900 | TAGAAATTGTACTTC[A/G]AGTGTATGTTAGTAA | 9690 |
rs138733906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227522 | GCCAGCATGGTGCAA[C/T]CCTGTCTCTACTAAA | 9690 |
rs138738277 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157157366 | GGAATATTTGTAGCA[C/T]CATGAAAATGATTAT | 9690 |
rs138753506 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157172999 | TTTCGGCCTCGAGCA[A/G]ATATCAAGCAAATTG | 9690 |
rs138755499 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157219166 | CTGCTGGTCTGAGAT[C/G]GTGTGTTGGCCTCCC | 9690 |
rs138763011 | snp | A/G | 4.95021e-05 | 0.0049748 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207398 | TTTCTTTAATTCAAG[A/G]TCTATGGTACCGTTG | 9690 |
rs138764090 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE3C | GRCh38.p7 | 7:157264066 | GTGAGCCAACATGCT[C/T]GGCCTGTTACACACA | 9690 |
rs138770050 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | UBE3C | GRCh38.p7 | 7:157224680 | TGGCTTCAAGAGTGT[A/G]TTTTTTAGGCCTATA | 9690 |
rs138778270 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157154357 | CCTTCTAAAGAGTAT[A/C]CATGAAATCATCTTC | 9690 |
rs138799797 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157251807 | GCTTAGCCTGAGAGA[C/G]AATTTTAAATTAAAA | 9690 |
rs138820394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157215041 | CTCGTTGAAGAAGGA[C/T]GGTATTTCCATAGCG | 9690 |
rs138923636 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | UBE3C | GRCh38.p7 | 7:157201393 | GTGATATATTAATAC[C/G]ATATGTAGCAGAGGG | 9690 |
rs138959964 | snp | C/T | 0.000115455 | 0.007597 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254056 | CTGAACAGGCAGATC[C/T]GCCAGCACTGCCTGG | 9690 |
rs138963752 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157140170 | CCCGCCCCTCCCTTC[C/G]CACCCCTTCCCATCA | 9690 |
rs139023962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240960 | GAGCTAAAATCTTGA[A/G]TTAAGGGGCAGTGAC | 9690 |
rs139030369 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157159010 | ATTAAGTCCGTTATC[A/T]ATAGAGTGTGAAATA | 9690 |
rs139031017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168876 | TCAGTGGTGATGGTT[A/G]CATAGCTCTTAATAT | 9690 |
rs139066221 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157264716 | TGGAATTATTACAGG[C/T]ATGCACCACTACAGC | 9690 |
rs139086581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202013 | TATATATTATAGAGA[G/T]TATGGTTTTATCTGA | 9690 |
rs139097731 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157196716 | GCTCACGCCTATAAT[C/T]CCAGCACTTTGGGAG | 9690 |
rs139139143 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157163751 | TTCTGTAATTTTTGT[A/G]TGGGAGTTTTAAAAT | 9690 |
rs139151219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157199247 | TTATTTTGAAAGTTC[A/G]TATTTTTCGTAGCTT | 9690 |
rs139160197 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157236232 | GGATGTGGTAATGTC[A/C]TCTTGAACTTTTTTT | 9690 |
rs139160520 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157192805 | AATGTTGTCTGACTA[C/T]TGCTTCAACAAACCA | 9690 |
rs139171151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202848 | CGGTGGTGGGAAGAC[A/G]CATCTCAGTTGTAGG | 9690 |
rs139171925 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269669 | GATTCTTTGTTCTTT[A/G]TTTTGTTTGCCCTTT | 9690 |
rs139213361 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157216147 | GACTCCATTTGCTTA[C/T]GTGAGGCAAGTGCTG | 9690 |
rs139222936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237765 | AATCTAAAAAATAGT[A/G]TTGGGTGCAGTAGCT | 9690 |
rs139223986 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157233633 | CAGTGGTGCATTTGC[A/G]TTGGGAATTTGCATT | 9690 |
rs139318207 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157183706 | GTAGGTGCTTTCTGA[A/C]ATGAACGGGGACAAA | 9690 |
rs139452805 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157261990 | TAGGAAATTCAATTA[A/G]CGTTATGAAAGAAAC | 9690 |
rs139454505 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157194566 | TCTGAGGCGCATGCC[A/G]GAAAGAAGCCAAATT | 9690 |
rs139477695 | in-del | -/AGGC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263591 | TTGCTTGAACCTGGG[-/AGGC]AGGCAGAGGTTGCAG | 9690 |
rs139497669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140921 | CACAAACACTAAAGA[A/G]ATCCTTGTGCAAGTG | 9690 |
rs139499938 | snp | C/T | 1.64985e-05 | 0.0028721 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182315 | CGTTTTAACTGTTGG[C/T]GAAAATTATTTGGGT | 9690 |
rs139514178 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157151984 | TGTGTATCCTATTTC[C/T]AGAACCCCAAGCAAG | 9690 |
rs139552195 | in-del | -/GGGA | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157154078 | TAATCCCAGCACCTT[-/GGGA]GGGAGGCCGAGGTGG | 9690 |
rs139562419 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157217272 | GCTTTTATTAGTATT[A/G]ATATATGTCTAGTAT | 9690 |
rs139562778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199366 | AGGCATATGGTAAGG[A/G]TTTTAAATATCTCAG | 9690 |
rs139566083 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264238 | CATGCTCGGCCTGTT[-/AC]TACACACACACACAC | 9690 |
rs139582619 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157149566 | CCTGAGAGTGAGTGC[C/G/T]TCCTTAAATTTGTGC | 9690 |
rs139589475 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157238567 | GAGGTCATGCTGACT[A/G]AGCTGGGAAAGGTGC | 9690 |
rs139600786 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157145014 | GGCCAGGTGTGGTGG[C/G]TAATGCCTGTAATCC | 9690 |
rs139627342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157252169 | AGAAATGTCAGTTTT[C/T]TCTGATCAGGCAAGG | 9690 |
rs139639074 | in-del | -/AC | 0.367978 | 0.220411 | intron-variant | UBE3C | GRCh38.p7 | 7:157264517 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs139662006 | snp | C/G/T | 0.0103379 | 0.0712359 | intron-variant | UBE3C | GRCh38.p7 | 7:157249628 | CGACAGAGCCTTTTA[C/G/T]GTGGTCTTCCTTCAC | 9690 |
rs139663360 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157141401 | GACGCTGTCACTAGT[C/G]CAGTTGGTTGTTGTG | 9690 |
rs139694368 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231109 | AAGCGGATCCGTGTG[C/T]ACTTGCTCAATGCCC | 9690 |
rs139707447 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UBE3C | GRCh38.p7 | 7:157245965 | CACTGCACACTCCAG[C/T]CCGGGCAACAGAGGG | 9690 |
rs139724025 | snp | G/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138763 | CACGCTAGCGGAACC[G/T]CCGGGAAGAGCGCCG | 9690 |
rs139726036 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157173416 | ATTAATCTTAACGTA[A/G]GGGAAAATGTCTCCT | 9690 |
rs139771616 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE3C | GRCh38.p7 | 7:157242845 | GAGAATCACGAGGTC[A/G]GGAGTTCTAGACCAG | 9690 |
rs139778388 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157246567 | CACCATAGCACTTGA[A/G]TCTTAAAACAGTAGG | 9690 |
rs139792176 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157220964 | CGGCCACCTCTTCAG[A/C]AGCCACCCATTTCTG | 9690 |
rs139793291 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157171457 | TTTTAAAAAAAATCC[C/G]AAATGTAATCGTAGT | 9690 |
rs139796651 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157152235 | TAGTCAGGGAGAGAG[C/G]TGGGGGAAAGGTAAT | 9690 |
rs139806998 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166466 | ATTTTGAGGGCTGGG[C/T]GCGATGGCTCACGCC | 9690 |
rs139834543 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157234555 | AAGGAATCAGTCTAT[C/T]CTGGATATAGAATAA | 9690 |
rs139839814 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157163112 | CAGAGATGGCCGGGC[A/G]CGGTGGTTCACGCCT | 9690 |
rs139865858 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157256411 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 9690 |
rs139867841 | in-del | -/A | 0.122064 | 0.214785 | intron-variant | UBE3C | GRCh38.p7 | 7:157255158 | ACAACGTACATGGGC[-/A]AAAAAAAACCAGATG | 9690 |
rs139900616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157265580 | AAGTGCCCAGCAACA[C/T]GTCGTGCCGCGCGTG | 9690 |
rs140020181 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157183185 | TTCAATTCTGATGCC[A/G]TCCACCCGGAGATAA | 9690 |
rs140072919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155267 | TTTACTCAAAGGCAA[C/T]GTTCTTTGAAGTGTA | 9690 |
rs140117895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217954 | CTTGTGCCCTGGAGG[C/T]GGAGGTTGCAGTGAG | 9690 |
rs140124747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261619 | GGGCTGCAGAATTAA[C/T]GTAGACTTAAAGGAA | 9690 |
rs140140679 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157152671 | GTCCAAATAATTTAG[C/G]AAAACCCCCAACACT | 9690 |
rs140193917 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157258500 | CTCTGTCGCCCAGGC[G/T]GGAGTGCAGAGGGCA | 9690 |
rs140204270 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157189613 | GCCCACTCAGCCCCG[C/T]GGCATTCCTGGCCTT | 9690 |
rs140209508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223785 | GTTAGTTGGGCGTGG[G/T]GGCATGTACCTGTAG | 9690 |
rs140214741 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157153387 | ACTCTGGAACCAACT[C/G]TCTGTGACTTAGCTG | 9690 |
rs140273785 | snp | C/G | 4.95356e-05 | 0.00497648 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174925 | CTGTTTCAGATATGG[C/G]TGTATCAGAACTTAA | 9690 |
rs140283409 | in-del | -/TG | 0.259397 | 0.249823 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137110 | CCTGGCTAATTTTTT[-/TG]GTATTTTTAGTAGAG | 9690 |
rs140297808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157195208 | AATTAGAGACGGGAT[A/T]TTCCAGGAAAGATAT | 9690 |
rs140329860 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157190372 | ATCTACTTGGTTGTC[A/T]GTACCTGCAGCCTGA | 9690 |
rs140362908 | snp | A/G/T | 0.00039919 | 0.0141226 | intron-variant | UBE3C | GRCh38.p7 | 7:157186785 | TGTAGTGTAGAGGAC[A/G/T]TTCCAGTTGAGCACA | 9690 |
rs140366266 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157232660 | CCTGGCCTGTTATTC[A/G]CATTCTTAAATAAAT | 9690 |
rs140427488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233125 | TTTTCTAGACATTTC[A/T]TATAAGTGGAATCAT | 9690 |
rs140437554 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE3C | GRCh38.p7 | 7:157139423 | GGGCTGGACTCGGGG[C/T]TGGACTCGGGGCCGA | 9690 |
rs140459866 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157266678 | TGTTTCTTCTCACCA[A/G]TGATTTGGTTAACCC | 9690 |
rs140471277 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157243438 | TTCTCTGAGTAACAG[C/G]TAGTGGGCTCTGCTC | 9690 |
rs140497385 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157171088 | AAAGTGCTGGAATTA[C/T]AGGCGTGAGCCACTG | 9690 |
rs140532774 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170358 | TTGTCACAGTCCGGG[A/G]GCGCTTTTCCCATTG | 9690 |
rs140562606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157211676 | TAAAATTTGGTTAAC[C/T]CTTGACAGCAGCAGT | 9690 |
rs140564262 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | UBE3C | GRCh38.p7 | 7:157167174 | GACCTCAAGTGATCT[A/G]CCCACCTCAGCCTCC | 9690 |
rs140579430 | in-del | -/ACACAC | 0.485118 | 0.0849685 | intron-variant | UBE3C | GRCh38.p7 | 7:157264407 | CATGCTCGGCCTGTT[-/ACACAC]ACACACACACACCTG | 9690 |
rs140611875 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157218009 | GCCTGGGTGACAGAG[C/T]GAGATTCTGTCTCCA | 9690 |
rs140654074 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157209694 | TTTTATGGCATCTGT[A/T]GAGAGTTTCATAATT | 9690 |
rs140657000 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157142574 | TCCAGGTTCGTGGAG[C/T]GGGGTGTGTGGAGTA | 9690 |
rs140686645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157205306 | GGTTTGAAGAGGACA[A/G]ATAAGTTTTTGTTGG | 9690 |
rs140687693 | snp | A/G | 0.046775 | 0.145601 | intron-variant | UBE3C | GRCh38.p7 | 7:157247008 | CGATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 9690 |
rs140762071 | in-del | -/C | 0.0554779 | 0.157039 | intron-variant | UBE3C | GRCh38.p7 | 7:157224690 | AGTGTATTTTTTAGG[-/C]CTATACACTCTATTT | 9690 |
rs140781707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157186655 | TAGGCAAAATGGATG[A/C]CTACTGTTGACTGGA | 9690 |
rs140842665 | snp | A/G/T | 0.00125029 | 0.0249726 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157187002 | ATGGTGCAGCACCGC[A/G/T]TGATGGTACCCAAAG | 9690 |
rs140919249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195773 | TTTGGATTTAGAGTT[C/G]ATGCTGTAATAATGG | 9690 |
rs140929712 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157159458 | TACCAAGTAAAAGGA[C/T]ACATTCAAAAGATCA | 9690 |
rs140962249 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157209230 | AGTCTCTCTCCAGCC[C/T]GTTCTGCCTGGTTTT | 9690 |
rs140963979 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | UBE3C | GRCh38.p7 | 7:157142280 | CTGGAGCTTAGTGGA[A/T]AATGGAGTGGTTACC | 9690 |
rs140976839 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184899 | AGAAGATATTCACTG[C/T]CAGGGCTCATGGCTG | 9690 |
rs140978722 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UBE3C | GRCh38.p7 | 7:157229592 | AAAGTGCTGGGATTA[C/T]AGGCATGTGCCACTG | 9690 |
rs141039829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263318 | CTAACGCCACCTTCC[C/T]GGGCATACAGAGAAT | 9690 |
rs141040668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226742 | TTTTTTTTACACAAT[C/T]TACCGTTGCCATTGA | 9690 |
rs141058800 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157240368 | CCAGCAAGCTGTGAA[C/T]AGGCTTCAATTAATA | 9690 |
rs141073306 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146218 | TCCTTTGTCAAAGAT[C/G]AGTTGGCTATATTTT | 9690 |
rs141088292 | snp | C/T | 0.00208079 | 0.0321879 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253998 | CATCCCTGTCACCAG[C/T]GCCAACCGGATTGCG | 9690 |
rs141098691 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157185689 | ATAAGCTCTTTTGCC[G/T]TTAGGTTTCTGTATA | 9690 |
rs141100307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146926 | AAAGTGCTGGGGTTA[C/T]GGGAGTGAGACACCG | 9690 |
rs141104100 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157250338 | ATTACAGGCGTACAC[A/C]ACCAAACCTGGCTAA | 9690 |
rs141106567 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157260039 | AATGAATAATAAAGA[C/T]GTATAAACTTAAACG | 9690 |
rs141107969 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180202 | AATTATAGTATTACC[A/G]TTATTTGTATTGTTA | 9690 |
rs141133256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198324 | ACTTGGAAGATTTGC[A/G]CTTCACTTCATCTTC | 9690 |
rs141156169 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157250842 | ATAAAAGCCTTCGGA[C/T]GGTGAGTGTTGTGGT | 9690 |
rs141166112 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204394 | CAAGAGGGAAACTTT[-/G]TTTCAAAAAAAAAAA | 9690 |
rs141166383 | in-del | -/C | 0.0788843 | 0.182262 | intron-variant | UBE3C | GRCh38.p7 | 7:157162969 | ACTTCCTTCTACAAA[-/C]CCAAGTCATTTTGTT | 9690 |
rs141166448 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157181059 | AAAAATGCACAAATC[A/G]GAGACAAATTATAAG | 9690 |
rs141168185 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157210716 | AAAGAACGCAGAAGC[A/G]TTTAGCCCATGATCT | 9690 |
rs141169927 | in-del | -/CA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155194 | CACCCCCTCCACACG[-/CA]CACACACACATTGTA | 9690 |
rs141183982 | snp | A/G | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248521 | AAGAGCTACGAAGAC[A/G]ATGTGGAGGAGCTTG | 9690 |
rs141280458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215231 | CGGGTAGGTCATTCA[A/G]GGGGTGTCCACATTG | 9690 |
rs141282578 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157148686 | CTTTTTCTTACAGAT[C/T]TGGCATCAAATAAAG | 9690 |
rs141306414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175338 | GGAAGGCCAGCCAAA[A/G]GAGGACTCCTGATGT | 9690 |
rs141336849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172191 | CTTATGCCACCACCC[A/C]TAGCTTAAATTTTTT | 9690 |
rs141337065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157251369 | TAGACGACTAATTTA[C/T]ATAGAACTCTTTCTA | 9690 |
rs141339604 | in-del | -/AAGAA | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157208393 | TATACCTTTTTAATT[-/AAGAA]AAGTAATTTTAGTAC | 9690 |
rs141369980 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157213618 | TGTGGAAAAAAGGAA[C/T]GTGTTAAGGTGTTTC | 9690 |
rs141390317 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236730 | TTGAACCCTAAACTC[-/T]TTTTTTTTTTCTCTT | 9690 |
rs141439113 | in-del | -/GAGAGAGAGA/GAGAGAGAGAGAGA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211167 | TTATCCATATGTCTG[-/GAGAGAGAGA/GAGAGAGAGAGAGA]GAGAGAGAGAGAGAG | 9690 |
rs141496509 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157261409 | TAATTGAGTTATACC[A/G]TGGAAAACACTTTGA | 9690 |
rs141499260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157241258 | CTGTGAGACCAGGAG[C/T]ACAAAAAACAAAAGG | 9690 |
rs141586362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200930 | CTAAAAATCTTTAAG[A/T]TACATTTTTTTAGAT | 9690 |
rs141605286 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157234438 | TGGGTCTGCCCTTAT[A/G]CAGTATGGTCTTGAT | 9690 |
rs141618918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140900 | AACTTAAGATACAGT[C/T]AGGTTCACAAACACT | 9690 |
rs141627680 | in-del | -/TGAATGTGG | 0.26326 | 0.249648 | intron-variant | UBE3C | GRCh38.p7 | 7:157192733 | AGAGTGCCCTTCTGA[-/TGAATGTGG]TGAATGTGGTGCTGG | 9690 |
rs141649057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244751 | GCTTCTACTATAATT[A/C]ATCCTTTTTATTTCA | 9690 |
rs141751506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157177566 | CCCTTTGCGTCCCAG[C/T]GGCTTGTTATGTGTA | 9690 |
rs141784243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220384 | TTTTTAAAGTGATCT[A/G]TTTTGCTTCATAAAG | 9690 |
rs141852448 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157182707 | TACATGCATGAATTA[C/T]TCATGAAAGAAATAT | 9690 |
rs141861829 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157152168 | AAGGGTGTAGGGAAA[C/G]TGGAAGAGAAGGCTG | 9690 |
rs141891444 | snp | G/T | 0.040671 | 0.13668 | intron-variant | UBE3C | GRCh38.p7 | 7:157256394 | GTGATCCGCCAGCCC[G/T]GGCCTCCCAAAGTGC | 9690 |
rs141895179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157188538 | CTTGCTTTTATTGTC[A/G]CACAACCCATTGCTG | 9690 |
rs141911196 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157256120 | TTATAGTTACAGGGT[A/G]ATCCTTATTCTAGCT | 9690 |
rs141928234 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157187437 | TGTTGCCCAGAGTGC[A/G]GTGGTGTGATCATAG | 9690 |
rs141939382 | snp | A/G | 0.000247555 | 0.0111228 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181555 | GTTGATTAACAGCAA[A/G]CTTCCATCAAGTATT | 9690 |
rs141941063 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157223467 | CTGATTACATAACAT[A/G]CTTTTCTCATTAGGC | 9690 |
rs141943161 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157153276 | CGCTAGATTGTTGGC[A/G]GTTAGTATGGTTCAC | 9690 |
rs141954063 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157267111 | AGTTAGAACTAAGCC[-/A]TCAATGTAATTTTTT | 9690 |
rs141985028 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157251941 | GGAGTTCAGACCAGC[C/G]TGGCCAACATGGTGA | 9690 |
rs141987052 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157183192 | CTGATGCCGTCCACC[C/T]GGAGATAATGTCAGA | 9690 |
rs142003351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218857 | AAAACAGCTAACTCT[C/G]AGTTCGCAAGGGTGC | 9690 |
rs142005425 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157150856 | AGCTTAAAGCAATAC[A/G]TTTTTGTTACCTTGG | 9690 |
rs142140245 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254077 | CACTGCCTGGCTTTC[C/T]GCCAGGGCCTTGCCA | 9690 |
rs142141208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251159 | GATTTCTGTAGAAAT[A/T]AATAGGTAGTCCTCC | 9690 |
rs142143749 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157202680 | AAAAAAAGAAGTCTA[C/T]GCCAATCCCCCTGTG | 9690 |
rs142175875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157242753 | CATAGAACTAGAAGT[C/T]GAGGAAAAAAAGGAA | 9690 |
rs142179299 | snp | C/T | 0.000261487 | 0.0114313 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207927 | AAAAGATGGATTCAG[C/T]TATTTAAGGTATAGA | 9690 |
rs142209101 | in-del | -/CT | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157142142 | AATTATGTTGAGCAC[-/CT]TACATATGCTTGTTT | 9690 |
rs142288557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157164343 | TAAGATTTTTACATA[A/G]ATAGGGTCTTGCTTT | 9690 |
rs142289236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212405 | CATACAGAAATGTCA[C/G]AATTTAGGATTAATA | 9690 |
rs142292306 | snp | A/G | 0.000335537 | 0.0129482 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267728 | TCTCTATGCGATTGA[A/G]TGTGCCGCTGGCTTT | 9690 |
rs142300323 | in-del | -/T | 0.44651 | 0.154543 | intron-variant | UBE3C | GRCh38.p7 | 7:157226719 | TTTTTTTTTTTTTTT[-/T]ACACAATTTACCGTT | 9690 |
rs142313565 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157205545 | AAAGAAGCCACCCCT[A/G]TCCAGTTAAGGCAGC | 9690 |
rs142361141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236054 | GATAAAGTGCAAAGA[G/T]GTCTTCAAGAGTGAT | 9690 |
rs142368430 | snp | A/G | 3.6001e-05 | 0.00424255 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267802 | ACCAGTGCTTCCTTC[A/G]TCAGCAGCGCCTCCC | 9690 |
rs142377611 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | UBE3C | GRCh38.p7 | 7:157165186 | TTATGGAAAATTCTC[A/G]GCCATTATCTCTTCC | 9690 |
rs142391923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202115 | ATGACTTTACTCCTC[C/T]TTTCACAGTGAAAAT | 9690 |
rs142415637 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | UBE3C | GRCh38.p7 | 7:157217971 | GAGGTTGCAGTGAGC[A/C]AAGATCGTGCCACTG | 9690 |
rs142446433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253607 | CTTTTTCTCTTCTGA[A/C]TTAACGGTGATTGTT | 9690 |
rs142459579 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157158808 | AATGCTTTAAAATCT[A/G]TTGTTGATTTTATGA | 9690 |
rs142506739 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | UBE3C | GRCh38.p7 | 7:157267227 | AGGAGTTCAAGACCA[G/T]CCTGGCCAACGTGGT | 9690 |
rs142553418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157227204 | AGTGTTTAGAGAAGA[A/G]TGAGATGTTTAACCT | 9690 |
rs142585741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157263250 | CCGGGCACCTGTCCT[A/G]ACGCCACCTTCCCAG | 9690 |
rs142590590 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157238350 | GTAAGTAGCTAGCAT[G/T]GGTCAAGCACTCAAG | 9690 |
rs142597713 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157166802 | ATTTGATTAAAATCT[A/G]TTGTTGGAGAATTAT | 9690 |
rs142613325 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157153915 | GGAGGACGGCTTGGT[A/G]GGGCGGGGGCGAGGT | 9690 |
rs142676221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151577 | TATGCTGCTTGGAAA[C/T]GCTTAGGTTCCTGCA | 9690 |
rs142708581 | snp | A/G | 0.000115719 | 0.00760565 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178835 | CAAATTTTGCACTAC[A/G]TGATTCACAATGGTA | 9690 |
rs142723951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144302 | CCCCATCTCTTAAAA[A/C]ATAAGGCAGGGGCAA | 9690 |
rs142728400 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157177891 | GAAACAGCCTCCTGG[A/G]TCCCTCATTAAAGGT | 9690 |
rs142728414 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | UBE3C | GRCh38.p7 | 7:157225176 | CCTGGCCGGATTTTT[A/T]AAATTTATTTTAAAC | 9690 |
rs142733499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266064 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 9690 |
rs142747221 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157247635 | AGGCGGAGGTTGCAG[C/T]GAGCTGAGATCGCGC | 9690 |
rs142758076 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157176935 | ACAGTCTTATCTGCC[A/G]CGTGCCAGAACATTG | 9690 |
rs142791600 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157173081 | TCCAGGAAAAGGATA[A/G]AAGAAAAGTGGGCTG | 9690 |
rs142791799 | snp | A/C/G | 0.00102373 | 0.0226016 | intron-variant | UBE3C | GRCh38.p7 | 7:157220827 | AATTACATGCTGTCA[A/C/G]ATTCACTCCTTTAAT | 9690 |
rs142811580 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157246473 | CTCTAGGTTGGAAGG[A/G]TGACTTCTGAGTTGA | 9690 |
rs142821132 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267633 | GGCTCCGACCTTGAG[C/T]GGCTCCCCACAGCCA | 9690 |
rs142821479 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE3C | GRCh38.p7 | 7:157174773 | CCTCTAAATAAAACC[A/G]ACTTAGAATATTTAC | 9690 |
rs142891275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157211992 | ACGGTTGTTTTCCAA[C/T]GAGGTCATGTTCTTA | 9690 |
rs142938121 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157179677 | GGAGGTCTGGAGAGC[C/T]GTGGCTGCAGACAGA | 9690 |
rs142970808 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157222357 | TACCATTTTTTTCTT[C/T]AATGAAATTGTGCTT | 9690 |
rs142972806 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157194005 | ACTGAACTGATATGA[A/C]CAAAATTTCAAATAA | 9690 |
rs142983545 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | UBE3C | GRCh38.p7 | 7:157190357 | GTGAACAGGCCCGTC[-/A]TCTACTTGGTTGTCT | 9690 |
rs142995458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168700 | AAAACCAGACACAGC[A/G]TATTGTATGATTCCA | 9690 |
rs143005759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143938 | AAGAGTCACACCTCC[A/G]GGAGTGGAGGAGAGT | 9690 |
rs143041390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153341 | AAAAGACGAAATTTT[A/G]GAAAGTGTAACCTTG | 9690 |
rs143062135 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157166383 | GCTCACTTATATCCT[C/G]AATTATTTTTCTGAC | 9690 |
rs143113172 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157197186 | TATTTACTACAGACA[A/G]ATTTTCAACTTATTT | 9690 |
rs143132419 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE3C | GRCh38.p7 | 7:157251167 | TAGAAATAAATAGGT[A/G]GTCCTCCTTACAAGT | 9690 |
rs143139509 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157182586 | GAGTTAAATGGGAAA[G/T]CTCTTCTGTGAGTCA | 9690 |
rs143172969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157193046 | TTGGTTCTGGTGTCA[A/G]TGCTGGAATGCTAGC | 9690 |
rs143182116 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157195559 | CCCAATTTCTGCTTT[G/T]TGAACAGGAATGTGT | 9690 |
rs143251196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233668 | CCACCTTTTAGCTAT[C/T]GTGAATAATGTTACT | 9690 |
rs143317496 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157204955 | CACGCAATTTGAAAA[C/T]CCTTGTTCTCAAGAT | 9690 |
rs143331127 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157159521 | TTAAAGCAAAATGGC[A/G]TTTTGGTTAGGAATT | 9690 |
rs143332946 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268375 | GTATACCGTGGCCTG[C/T]CTCATGATGGTTTGG | 9690 |
rs143333272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232031 | TTTAGAGGCTCTAGA[A/G]GAATCCATTCTTCTG | 9690 |
rs143356678 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177929 | TTTTTTTTTTTTTTT[-/T]AAGAAAAAGGAAAAA | 9690 |
rs143401608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157265593 | CACGTCGTGCCGCGC[A/G]TGTGCATGGAACACC | 9690 |
rs143417215 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157210232 | GTGGTGATTGTTTTA[A/G]GTTTGAAATCAAGTT | 9690 |
rs143420504 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157172679 | AGTTAAGTGCAGGCT[C/G]TTTCCAGGCTTGCTT | 9690 |
rs143422619 | in-del | -/G | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157173359 | CCAGCCTGGGCGGTT[-/G]AATGTTGATTCAGTT | 9690 |
rs143453980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214157 | TCCATGGTACTGGCA[C/T]GTTATATTGGTAACA | 9690 |
rs143528026 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157214624 | AATTTAATTGGTCAC[A/G]AAAATGGAAAGACCA | 9690 |
rs143534040 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147212 | TTATTTCTTTCATTG[A/G]TTATATAATTTTCCT | 9690 |
rs143560664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219376 | CTTGAAGTAGGTTTC[A/C]CTTCTGCAGTGAAAA | 9690 |
rs143560765 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157149392 | AAATAGAAACCAAGC[A/G/T]GAATGGAAGGAGTGA | 9690 |
rs143563548 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157151173 | TCTGTGGACATAATC[C/T]TGAAGCCACCGTAGA | 9690 |
rs143591506 | in-del | -/T | 0.0138799 | 0.0821421 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269357 | CATTTACATTAAATG[-/T]TTTTTTTTCCCAAGA | 9690 |
rs143594017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157211360 | ATCCAAAGCTTGTAG[C/T]GCTGTGCCTTATCCT | 9690 |
rs143597883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144735 | AGTTTCAGGTTTACA[A/G]TCAAGCAGAGGGTAG | 9690 |
rs143608582 | snp | C/T | 5.00881e-05 | 0.00500415 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186921 | AACACCCTGCTCAAC[C/T]TGGTGTGGAGGGACT | 9690 |
rs143632964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235885 | TAACCATTGCTCGGA[C/T]CTAAGTAAGTGTCAT | 9690 |
rs143664388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157247697 | ACTCCGTCTCCAAAA[A/G]AAAAAAGAGCATAAG | 9690 |
rs143689227 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157248781 | CAGTTCCTGCTCCCA[C/T]GCATGAAGCCTGTTC | 9690 |
rs143689426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157142379 | GTACGACAAGTCTGA[C/T]TTGAAGAAGTTGATA | 9690 |
rs143691260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178550 | GGATGATTTCCCTGT[C/T]TATCTGTAAGATGTC | 9690 |
rs143699018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228889 | TCAAAATTACTGACA[C/T]GTGTACATAGCAATC | 9690 |
rs143704281 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157247843 | GGTTATGAACTGGGA[-/C]CCCCCCAAAACTGTG | 9690 |
rs143728434 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157246100 | GAAAACCTCAACAGC[A/T]ATTTTCTCATTTTCT | 9690 |
rs143732222 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157239953 | GGATGGGAAGAGCAG[G/T]GTTCCCAGACCAGCC | 9690 |
rs143756267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157246696 | TGTCCTTCCTGCCGT[C/T]CCTCATTCTCGGGCA | 9690 |
rs143917323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233346 | CCTAGGCTGGAGTGC[A/G]CTGCTACAAACACGG | 9690 |
rs143919435 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161195 | CAGTGTTAATTTCCT[A/G]TGGATAATTGTATCT | 9690 |
rs143944292 | snp | A/G | 0.0383715 | 0.133092 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137023 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 9690 |
rs143958665 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157229363 | CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCACA | 9690 |
rs143962519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157158367 | TTGAAACCGTAAGCC[A/G]TAGCACCCAAAACCT | 9690 |
rs143979768 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | UBE3C | GRCh38.p7 | 7:157241992 | GTGAGTGATCGCCAG[C/G]GCTGGGAGGAACCAG | 9690 |
rs143983919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170772 | GCCAGCACGCCTAGG[G/T]CAGTGGGACGTGCAC | 9690 |
rs143985915 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157147552 | ACCATCAGAAAGCAA[C/T]GTGTTTTATTGTCTT | 9690 |
rs144031734 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157265268 | GATACTAAATCTGCA[C/T]AGGCTGCGACAGTGA | 9690 |
rs144076364 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195273 | ATGACATATGTAAGA[A/G]ACCCACAAGTTTCTC | 9690 |
rs144090192 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157261868 | TGATTTTTCTCACTC[A/T]GAATTAATGCAAATT | 9690 |
rs144183418 | in-del | -/C | 0.0456336 | 0.143994 | intron-variant | UBE3C | GRCh38.p7 | 7:157190549 | ACAGATTAGAACACA[-/C]CCACCCTCACGGAAG | 9690 |
rs144185326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157174238 | GTGGTGGCGGGCACC[C/T]GTAATCCGAGCTACT | 9690 |
rs144198106 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223267 | AGTGGGTTTGGAGTC[C/T]CCGCCGCTGTCTGTG | 9690 |
rs144226991 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157223740 | GCCTGGGAAACATAG[C/T]GAAACCCTGTCTCTA | 9690 |
rs144237967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248126 | TCTTCATAATTCCAC[A/G]ATTTCGCTCCTAGGT | 9690 |
rs144241203 | snp | C/T | 0.021333 | 0.101051 | intron-variant | UBE3C | GRCh38.p7 | 7:157154698 | AAGAAAGTCTCTTGG[C/T]GTATATTGTGATATT | 9690 |
rs144273724 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157192746 | TGATGAATGTGGTGC[A/T]GGAGTGTTTATGGCA | 9690 |
rs144334416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253183 | TAATCACAGCAATTC[C/T]AAGTCAGACAAACAA | 9690 |
rs144349300 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157213010 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAATGCT | 9690 |
rs144359805 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157252398 | AATTAAGATAATGAA[C/T]ACAATCTTTAATCAG | 9690 |
rs144368932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145838 | TCAAAACCTCCTCTC[C/T]GCTGCACGCTGTTTC | 9690 |
rs144378723 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBE3C | GRCh38.p7 | 7:157198114 | GGTTCATTGTAAGGT[C/T]TCAATTCTCCATCAT | 9690 |
rs144428498 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157249836 | AGTTAGTAACATCTG[A/G]GATTTGCTTCAAATA | 9690 |
rs144443687 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248445 | TGGAACCAGTGCCGA[C/T]GTGGACATTCACCAC | 9690 |
rs144449489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171219 | CAACCTTCCCCTCCC[A/G]GGCTCAAGCAATCGG | 9690 |
rs144515105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167235 | CATGCCCGACCTCAC[A/T]GGATTTTTTTATAAC | 9690 |
rs144580323 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157243075 | AAAAAGGAAGCGTCA[A/G]CTCCAAGCTGCTCAA | 9690 |
rs144642146 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157239483 | CAAGGTGCTAGGCAT[G/T]TTCTGCGCTGTGGAC | 9690 |
rs144647838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157212365 | TTTTTTGGTTGCAAT[A/G]CTATATCTAAATATC | 9690 |
rs144678971 | snp | C/T | 0.000760342 | 0.0194831 | intron-variant | UBE3C | GRCh38.p7 | 7:157216845 | CTCACGTGTGTGACG[C/T]GGATATGTTCTTTCT | 9690 |
rs144788199 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157221512 | CTTTAGGAGGCCGAG[A/G]TGGGCGGATCATCAG | 9690 |
rs144792083 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBE3C | GRCh38.p7 | 7:157227465 | GCACTTTGGGAGGCT[A/G]AGGCAGGCAGATCAC | 9690 |
rs144822292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157233817 | TTACAATCCCACCAA[C/T]AATTTGTGAAGGTTT | 9690 |
rs144832592 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157162255 | GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCTC | 9690 |
rs144846986 | snp | C/T | 0.000149337 | 0.00863979 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170360 | GTCACAGTCCGGGGG[C/T]GCTTTTCCCATTGCT | 9690 |
rs144856679 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBE3C | GRCh38.p7 | 7:157267503 | TACTGATTGGAGCAG[A/G]CACATTTTGTGTACT | 9690 |
rs144879410 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205334 | GGTTAATTACCCTGT[-/C]CCCTTTTTTTTTTGG | 9690 |
rs144894620 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157189942 | AGTAGCTGAGATTAC[A/G]GGCACCCATCACCAT | 9690 |
rs144924708 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157184961 | GTTTTTATAGTGGAC[A/G]GTGGATGCTGGAACT | 9690 |
rs144932224 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260384 | CACGTCCAGGTTCGT[A/G]TGTGAAGAAATAGAT | 9690 |
rs144933531 | snp | C/G | 0.00138538 | 0.0262825 | intron-variant | UBE3C | GRCh38.p7 | 7:157231356 | CATATAAAAATAGAC[C/G]TCGGACCAAAAGATG | 9690 |
rs144984506 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157258608 | GTGATTACAGGCGTG[C/T]GCCTCCATGCCCGGC | 9690 |
rs145050243 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBE3C | GRCh38.p7 | 7:157254892 | TAAAAATTAGCTGGG[C/T]GTGGTGGCATACACC | 9690 |
rs145062247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164322 | CCACCATGCCCAGCT[A/G]ATTTTTAAGATTTTT | 9690 |
rs145085428 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157140165 | TTGTTCCCGCCCCTC[C/T]CTTCCCACCCCTTCC | 9690 |
rs145110205 | snp | C/G | 0.000230985 | 0.0107443 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231246 | TAATGAAGGGCTTCT[C/G]TACCCCAACCCGGCT | 9690 |
rs145119997 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157243753 | GAAATGGGTGTTGAC[A/C/G]TATACATAACCTGAA | 9690 |
rs145120218 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157172544 | CCAGCATTGCCTCCA[G/T]AGTTGAGCTAAGGTG | 9690 |
rs145152662 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157168769 | GAAGTAGATGAGTGA[C/T]TGCCAGGGGCAAGAG | 9690 |
rs145179232 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186430 | CAAAAAAAAAAAAAA[A/T]TTATGTAATACTCTC | 9690 |
rs145229466 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157204550 | ATTCTTCACCCCAGT[C/G]TAGCAGACCACATTT | 9690 |
rs145260126 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157206631 | TCTGGCTCTGTTCCC[A/C]AGGCTGGAGTGCAGT | 9690 |
rs145263012 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157141403 | CGCTGTCACTAGTCC[A/T]GTTGGTTGTTGTGGG | 9690 |
rs145277242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157243676 | AGCTGTGTAGACCAA[A/G]TGTTGCGGGAGTTGA | 9690 |
rs145291088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149714 | AATAGATGGTCTCAT[A/T]AGACCATAGAATAGC | 9690 |
rs145291516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203111 | CCTTTATGATGGGAC[C/T]GGTGTTCAAATCATC | 9690 |
rs145328501 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157208803 | GGGATGGAAAAAAAG[A/G]AAAGGAAAAGGGTGC | 9690 |
rs145359477 | snp | A/G | 0.000233361 | 0.0107993 | intron-variant | UBE3C | GRCh38.p7 | 7:157184077 | GATGCAGGCAGCCCC[A/G]TCGGATCTTCTAGCT | 9690 |
rs145368482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204189 | TCATATTTCCTACTG[A/G]GAATAAAGTTTAAAA | 9690 |
rs145417774 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157247419 | ACTTTTGGCCGGGCA[A/G]GATGGCTCACACCTA | 9690 |
rs145460288 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157250839 | GGCATAAAAGCCTTC[A/G]GACGGTGAGTGTTGT | 9690 |
rs145488990 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157247139 | GATCCAGCCGCCTCA[C/G]CCTCCCAAAGTGCTG | 9690 |
rs145535655 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157232913 | TAACTCACATTATGG[A/T]AAATTGAACCTTTTA | 9690 |
rs145545553 | snp | C/T | 0.000358461 | 0.0133829 | intron-variant | UBE3C | GRCh38.p7 | 7:157187056 | TGTGCCAGGGGGTGC[C/T]AGCCAGAGAACATAC | 9690 |
rs145565311 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157159567 | GTTGTATCAGAGAAC[A/G]TGATTAAATACCATT | 9690 |
rs145586289 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | UBE3C | GRCh38.p7 | 7:157226051 | AAAAAATATTAATTA[C/T]TTTTAAAGGGCAAGA | 9690 |
rs145591993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155639 | ATAAAGAATAAACTT[C/T]GTTACCACTAAATTT | 9690 |
rs145593619 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157265670 | GATGAGAAAAGCACG[A/G]CACGGAATACTGTGT | 9690 |
rs145609937 | snp | C/T | 0.154661 | 0.231107 | intron-variant | UBE3C | GRCh38.p7 | 7:157227552 | AAATACAAAAAAAAA[C/T]AGCTGGGCGTGGTGG | 9690 |
rs145655077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157152903 | TGCAGCTTTAACGTT[A/G]TTTAATTTTTTGCCA | 9690 |
rs145728471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180270 | AACAGAACCTTTGTC[A/G]TGTTGTCAGTCTATT | 9690 |
rs145780313 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:157209477 | AAGATTGACAAATTT[A/G]CAATTTTTCTATGTT | 9690 |
rs145793992 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157176564 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCAAACC | 9690 |
rs145822639 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157209889 | TTGAAAGTTTTAAGA[A/G]TTAGGGCAAGGCCGG | 9690 |
rs145829186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142788 | ACACCCCAAACCTCC[A/G]CGTCCTGCAGTATAT | 9690 |
rs145837581 | snp | A/G | 0.00135026 | 0.0259482 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201795 | CTTCCATGTCAACAC[A/G]GATGATCACAGGGTA | 9690 |
rs145857759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218961 | AAAAGAAGTACTCAA[A/G]CATTTAACCCACCTT | 9690 |
rs145876103 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | UBE3C | GRCh38.p7 | 7:157247147 | CGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 9690 |
rs145879933 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157213855 | AATTGAATTACGGAT[A/T]AATCACAATTACTTT | 9690 |
rs145887398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205346 | CTGTCCCTTTTTTTT[C/T]TGGACCCAATATAAG | 9690 |
rs145887774 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | UBE3C | GRCh38.p7 | 7:157140576 | GACTTCAGAGAATCT[C/G]AGGGCCAAATCGCCT | 9690 |
rs145907373 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157214945 | TGTATGTGCAGCTAA[A/G]CCCCTGAGCAACACC | 9690 |
rs145915780 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157244100 | GCTGGGCATGGTATG[C/T]GCACTTGTAATCCCA | 9690 |
rs145941800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157163050 | TCTTCATTGAAATTT[C/T]TATTGAGATAATTGT | 9690 |
rs145961178 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267858 | CACGCCTGAGGCTCT[C/T]CTAAGCTCCTTCTTT | 9690 |
rs145979991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265397 | GTATACGAGGAAGGT[A/G]GAGTCACCGGTTCTT | 9690 |
rs146041717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220405 | CTTCATAAAGCAATT[A/G]TATTATTTTACTATG | 9690 |
rs146081202 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157256468 | CCTCCTTAAGTTGCT[C/T]TCCCCTTCTCGTACT | 9690 |
rs146166594 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157166405 | TTTTCTGACTTCTTT[A/G]TATTTTTCAGAATTC | 9690 |
rs146183086 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157241269 | GGAGCACAAAAAACA[A/G]AAGGAAAAATGAACT | 9690 |
rs146186008 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157198359 | AGTTCTTCCAAGGCC[A/G]GTTTATTTCTTGATA | 9690 |
rs146271756 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200708 | GGTGCAATCTTGGCT[A/C]ACTGCAGCCTTGAAC | 9690 |
rs146288930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151966 | TTCTGTTCTAGTACC[A/G]TGTGTGTATCCTATT | 9690 |
rs146308446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157149453 | TTTCTTTGGACATTA[A/G]ATCTGGGCCTACAGG | 9690 |
rs146377009 | snp | C/T | 0.000709881 | 0.0188265 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254097 | GGGCCTTGCCAATGT[C/T]GTCAGCCTCGAGTGG | 9690 |
rs146407950 | snp | C/T | 0.00946478 | 0.0681381 | intron-variant | UBE3C | GRCh38.p7 | 7:157201818 | ACAGGGTATGTATTA[C/T]ACAGACTTATAAATT | 9690 |
rs146448156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159289 | AAGTTAGGAGTATTT[A/G]ACACAGCAGGCATGT | 9690 |
rs146467256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156680 | CTGTTCTCTACATAC[A/G]TAATCATATAGGTGT | 9690 |
rs146469444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157199335 | AAAGGCAAGAAAAAA[C/T]GTTAACACTCTTATC | 9690 |
rs146485586 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157263296 | CCACCTTCCCCGGGC[A/G]CCTGTCCTAACGCCA | 9690 |
rs146487736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195274 | TGACATATGTAAGAG[A/T]CCCACAAGTTTCTCG | 9690 |
rs146505928 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157259652 | ATTATATGTAATTCC[A/T]CTCGGATAAACTGTC | 9690 |
rs146525747 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157236164 | TGTGGGTCATGATTG[C/T]ATTTTGTCGCCTGTA | 9690 |
rs146568780 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | UBE3C | GRCh38.p7 | 7:157175179 | CATGGACTTCTGTAT[A/G]TATTACAATTTTTAC | 9690 |
rs146587249 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157217824 | CCTGGGTGATAAGAG[C/G/T]GAAATTCCGTCTCAA | 9690 |
rs146605379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213142 | ACGTTTTGATCTGGC[A/G]TGGAAGAACATGAGA | 9690 |
rs146657919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233489 | CTTGCCATGTTGCCC[A/G]GGCTGGTCTTGAACT | 9690 |
rs146686892 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157195202 | AGCCAAAATTAGAGA[C/T]GGGATTTTCCAGGAA | 9690 |
rs146722830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232334 | TTTATAAAGTTGAGT[A/G]TTCAGGAATTGTTAT | 9690 |
rs146750630 | in-del | -/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170134 | TTTTTTTTTTTTTTT[-/C/T]CTTTTTAACCATTTT | 9690 |
rs146755594 | snp | A/G | 0.00404451 | 0.0447872 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183961 | GTCTCTCCTGCCAGC[A/G]CGAGCTGTCACGACT | 9690 |
rs146760960 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157263500 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 9690 |
rs146771781 | snp | A/C | 3.29886e-05 | 0.00406118 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163830 | AAAGGCTTCTCTTTT[A/C]CATCGTACTCAGGAA | 9690 |
rs146810102 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157145715 | AAGGCTCTTTTCATG[A/G]CTTGACAGTTCATTT | 9690 |
rs146824340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157249311 | GTGGACACTTCACAT[C/T]GATAGAGTCTTTTTT | 9690 |
rs146828901 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157142555 | GTGGAAGACGAGAAG[C/G]CATTCCAGGTTCGTG | 9690 |
rs146829617 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157179138 | TTGTCCCGTCATCCA[A/G]GATTGGTGTCTGCAG | 9690 |
rs146843759 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157246955 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA | 9690 |
rs146848489 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157175432 | AATACACCTTTCATC[A/G]GGCTTTTTATTATTT | 9690 |
rs146863631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157244007 | GAGGCCGAGGCGGGT[A/G]ATCACCTGAGGTCAG | 9690 |
rs146920198 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157150333 | GCAGTGAGCTGAGAT[C/T]ATACCACTGTCCTCC | 9690 |
rs146935930 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157186215 | GATCATTTGAGGTTA[A/G]GAGTTCGAGACCAGC | 9690 |
rs146936406 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157146940 | ACTATGGTTGGGCGC[C/T]GTGTCTCACTCCCGT | 9690 |
rs146952756 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | UBE3C | GRCh38.p7 | 7:157181763 | ATTTTAAATATAGAC[G/T]TGAAATTCAGGTTTT | 9690 |
rs146953370 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157251110 | AATTAAGAAATTCAC[C/T]AGTGAAGCACCTAAT | 9690 |
rs146957627 | snp | A/G | 6.59239e-05 | 0.00574087 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248577 | TGACCTGGGAGAGGC[A/G]CAGGTGAGGGGTCAG | 9690 |
rs146963570 | in-del | -/CA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264132 | TCAGCCTGTTACGTG[-/CA]CACACACACACCTGG | 9690 |
rs146971871 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157177020 | TGACTAATCACATAC[A/T]TATTTTTTAATGCCG | 9690 |
rs147025939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164472 | TGATGTTGATGTTTC[A/C]TGAAGCATAAGGAGA | 9690 |
rs147041706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160344 | CCTCCCAAAGTACTG[G/T]GATTACAGGTGTGAG | 9690 |
rs147057469 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157266743 | CTTGATCCTTTTTAA[A/C]AAATTTTTATAGACA | 9690 |
rs147058190 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157201031 | TTTACAAATTTTAAA[C/T]GTGTTAAGTAGGCCA | 9690 |
rs147074241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264346 | GTGTGAGCCAACATG[C/T]TCGGCCTGTTACACA | 9690 |
rs147195291 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157211371 | GTAGCGCTGTGCCTT[A/G]TCCTTTTCTGTTATT | 9690 |
rs147211425 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157207270 | TTACCTTGCCTTTAA[A/G]TAGTTTAATTCCTAA | 9690 |
rs147226419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246332 | GGCTCACAGTTGAAA[C/T]GTTTCTCCTTTGCTG | 9690 |
rs147286905 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157161483 | TTGAGACAGGGTCTC[A/G]CTTTGTGACTCCAGC | 9690 |
rs147303711 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157158538 | CTGTGATTAAAAGTG[A/T]TGATTAGTCACAAAG | 9690 |
rs147318916 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157226502 | CTGGATCTAAAATTA[A/G]AAATGAAATCATCTT | 9690 |
rs147319704 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157155661 | ACTAAATTTATTTAG[G/T]GAAGAAAGCATTTTC | 9690 |
rs147332938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157261887 | TTAATGCAAATTCCC[A/G]TTGTACTGTATTTAA | 9690 |
rs147376489 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157144546 | AGGCAATGGGAAATA[C/T]TTTGAGACTTAAAGA | 9690 |
rs147409767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173256 | GTAGCTTGCTGCTGT[A/C]GTCCAGCTACTTAGG | 9690 |
rs147426071 | snp | A/G | 0.084364 | 0.187256 | intron-variant | UBE3C | GRCh38.p7 | 7:157171318 | TTTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 9690 |
rs147479278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158232 | TGCGAAGAAAATTCA[A/G]AGGAAACACAAATAT | 9690 |
rs147494825 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157155163 | TTATTTCATGTAGGT[C/G]TGCAAAAAAGAATCC | 9690 |
rs147512158 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBE3C | GRCh38.p7 | 7:157193352 | AGATCATTGGGTGTC[C/T]CGCTGTTTCTTTTAC | 9690 |
rs147528239 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157189569 | GACTGCATTTGTGAC[C/T]CTACTTACATGTAGA | 9690 |
rs147528844 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | UBE3C | GRCh38.p7 | 7:157257629 | GTAATCCCAGTTACT[A/T]GGGAGGCTGAGGCAC | 9690 |
rs147532844 | snp | A/G | 1.65534e-05 | 0.00287688 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178845 | ACTACATGATTCACA[A/G]TGGTAAGTAGTAGGC | 9690 |
rs147559720 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157258609 | TGATTACAGGCGTGC[A/G]CCTCCATGCCCGGCT | 9690 |
rs147561849 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE3C | GRCh38.p7 | 7:157218717 | GGGGAAGACCCTGCA[A/G]GATGGGTGTGGAGTG | 9690 |
rs147563185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157150855 | GAGCTTAAAGCAATA[C/T]GTTTTTGTTACCTTG | 9690 |
rs147650334 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157203791 | GACAGTGTATTAATG[C/T]GTTCCCAATACAGAT | 9690 |
rs147664303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235961 | AGAAGAAAACTGTAT[A/G]TTGATTGATTGTGAT | 9690 |
rs147668509 | snp | A/C/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157165105 | CACCAGAAACTACCA[A/C/G]ATGTCCCAGGGAGGG | 9690 |
rs147701036 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157189932 | AGCCTCCCGAGTAGC[-/T]TGAGATTACGGGCAC | 9690 |
rs147722444 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142143 | ATTATGTTGAGCACC[C/T]ACATATGCTTGTTTT | 9690 |
rs147755224 | snp | C/G/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157152969 | GGGAGGCTGAGGGGG[C/G/T]TGGATTGCCTGAGGT | 9690 |
rs147772790 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157180748 | AGAAGCGTAGGCTGG[A/G]TATTTTAAGAGGTTC | 9690 |
rs147794730 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248463 | GGACATTCACCACCT[C/T]GCCTCCCTAGACCCT | 9690 |
rs147828279 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137810 | TTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAG | 9690 |
rs147860115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238886 | GAAGTGGGATTTCAG[A/G]TGCCAAATAAAGACA | 9690 |
rs147861257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167260 | TATAACCATTTCAAG[C/T]CCAGGAACTACATCT | 9690 |
rs147874479 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157243319 | CTGTGAGGCCTCGGC[A/G]GCTCTGCATGCTGGG | 9690 |
rs147891353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239689 | GGAAAGCTGTGTTCT[A/G]AAGATGGGAGAAATA | 9690 |
rs147932565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157152537 | ACATGCAGATCCTTG[C/T]GCTCCTCACTATTTG | 9690 |
rs147977568 | snp | C/G/T | 0.000247247 | 0.0111163 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267677 | CCTGCTGAAGCTCCC[C/G/T]GAGTTCTATGACGAG | 9690 |
rs147979796 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157244189 | GAGCTGAGATCGTGC[C/T]ATTCATTGCGCTCCA | 9690 |
rs147980845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172818 | AGATCACCAAGGAGC[A/G]CAGACAGGCAGGTGC | 9690 |
rs148031044 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157177158 | CTCCATATCCTGAAC[C/G]CTTGGTATTGACATT | 9690 |
rs148036563 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208223 | GGGCTACTGGCACAT[-/G]GCCACCACACCCAGC | 9690 |
rs148047340 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157219404 | AAAGCAGAGATGGGG[C/T]CTCTCAGTGATCGAG | 9690 |
rs148103526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157188522 | CAGCTGAACCAGGAC[A/G]CTTGCTTTTATTGTC | 9690 |
rs148176792 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157140776 | GGAGTGCATCTCTGC[C/T]CTGAGGGAGTGAGAT | 9690 |
rs148190803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210571 | TGTTTTACAGATGAG[G/T]TCATGTATATGATGG | 9690 |
rs148194590 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157144278 | TCCAGCCTAGGCGAC[A/C]CAGCATGACCCCATC | 9690 |
rs148245030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147864 | TTAGAATATTGAGCC[C/T]GTCTTGCGTATCTGG | 9690 |
rs148262061 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157251232 | AATATGCAAATACTT[C/T]ATTGTGTCAGCAGGT | 9690 |
rs148330819 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157261130 | CAACATGATGAAACC[C/T]CGCCTCTACTAAATA | 9690 |
rs148350660 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157204992 | AGAGGTTAGGGATTG[C/T]CTCGGGTCTCACTGA | 9690 |
rs148432386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263183 | TTTCCCGGAAAATCA[C/G]CTTAGTCTGCCCACC | 9690 |
rs148434858 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166608 | ACCCAGGCATGCTGG[C/T]GCATGCCTGTAATCC | 9690 |
rs148503183 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157174654 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 9690 |
rs148503899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246437 | TAATATTTACAGTGC[A/G]TGATATGGTTGGGTG | 9690 |
rs148556313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179643 | AGCATTAAAAATGTG[C/T]GTGAGACTAGTTGTG | 9690 |
rs148572341 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157221518 | GAGGCCGAGGTGGGC[A/G]GATCATCAGGTCAGG | 9690 |
rs148590760 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142142 | AATTATGTTGAGCAC[A/C]TACATATGCTTGTTT | 9690 |
rs148591851 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157233981 | GTGCTTCATGACTTC[G/T]GTTGAGAAATGTCTA | 9690 |
rs148597222 | snp | A/G | 0.000115801 | 0.00760836 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181534 | GTATTATAGGTCTCT[A/G]TATTTGTTGATTAAC | 9690 |
rs148646123 | snp | C/G | 0.0225045 | 0.103662 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137479 | CCCATGTTGGCGAGG[C/G]TGGTCTCAAACTCCT | 9690 |
rs148661073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242279 | TGGAAGGAGTATAGT[C/G]ATTAGAGCATGAGCT | 9690 |
rs148696297 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157141499 | GGTACAGCCCGTTGC[C/T]CCTATGCTACACACC | 9690 |
rs148708650 | snp | A/G | 3.34219e-05 | 0.00408777 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267722 | TAAACTTCTCTATGC[A/G]ATTGAATGTGCCGCT | 9690 |
rs148713734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157212381 | CTATATCTAAATATC[C/T]GTCATCTCCATACAG | 9690 |
rs148727633 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UBE3C | GRCh38.p7 | 7:157248194 | ATTGAATGCCTGCAC[A/G]GGATCCTGGAGCACA | 9690 |
rs148732363 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157154778 | GAAGCAGAAGGAGTG[A/G]AGAAGGAACAAAGAA | 9690 |
rs148761004 | snp | A/G | 0.00555807 | 0.0524227 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207903 | CAACAATGCATACAG[A/G]TGGAACAGAAAAGAT | 9690 |
rs148768294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149826 | CCTAGGAATTTGGAA[G/T]TGGGGCATCTTATTC | 9690 |
rs148783219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157253377 | TGTGAGTATAGCCAC[A/G]TACTAATAAAAAGTG | 9690 |
rs148786644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157158598 | TCTAATGATTTAGCT[C/T]ATTGTCCATTTTTAG | 9690 |
rs148816296 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157214133 | CGCCTTTTTTTGATT[A/G]ACCAAGGATCCATGG | 9690 |
rs148834239 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227027 | ATTAGCAGATTTCAC[A/G]TTCATCTCTCCCACT | 9690 |
rs148838274 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157156449 | GTAGCTGGGACTACA[G/T]GCGCATGTCACCACC | 9690 |
rs148888486 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157159578 | GAACGTGATTAAATA[A/C/T]CATTTGCAGCTGGGT | 9690 |
rs148904924 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157200600 | AGTTCATCTTTTTTA[A/T]ATCTAATATTATAGA | 9690 |
rs148905146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265727 | AACCTAAAGGAGGGA[A/G]AACATTTTCTCATGC | 9690 |
rs148924558 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157221737 | CAGTATAAGACTGTC[-/T]TAAAAAAAAAAAATT | 9690 |
rs148957726 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157239946 | AGAGCAAGGATGGGA[A/G]GAGCAGTGTTCCCAG | 9690 |
rs148977395 | in-del | -/AG | 0.0418186 | 0.138422 | intron-variant | UBE3C | GRCh38.p7 | 7:157240108 | GGTTTTTTGAGACAG[-/AG]TCTTGCTCTTGGCAT | 9690 |
rs149009065 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157172594 | TGTAAACCGAGAACG[C/T]GCAGAGAAGGAACTG | 9690 |
rs149026482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157247497 | AGGAGTTTGAGAAAA[A/G]CCTGGCCAATATGGC | 9690 |
rs149027619 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157176258 | CAGAGCAAGACCATG[C/T]TTCTTTTTTTATTAT | 9690 |
rs149082361 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231267 | CAACCCGGCTGCTCA[A/G]ATGCTTGTGGGAGAT | 9690 |
rs149094145 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | UBE3C | GRCh38.p7 | 7:157224430 | CGATCTCCTGACCTC[A/G]TGATCTGCCTGCCCC | 9690 |
rs149098325 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157195379 | ATAAGCTGATACTCA[A/G]CTGCAAACATGTGCT | 9690 |
rs149112065 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157235308 | ATAAAGGTGAGTGTT[A/C]TGCTAGACTAACCTG | 9690 |
rs149168946 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157140048 | TAAGGGTAGGCAAAC[C/G]ATGACGCCTCTGTTC | 9690 |
rs149178042 | in-del | -/AG | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157195855 | TGAATCTTTTAACAC[-/AG]GGGTGGAGTGGTGGC | 9690 |
rs149182107 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157243711 | GTAGAAAGCTCTCTG[A/G]AATAGGATTGTGAAG | 9690 |
rs149223346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143501 | CCTGTCTCCTTCATT[C/G]CTGGCTCTGCAGACT | 9690 |
rs149269958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206209 | TTAAAAACGAGAGAA[A/G]AGGAAGAAGTTCTAG | 9690 |
rs149274015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157141012 | AGGCTAGCGTTAACC[C/T]CATCTCACCAGGAGC | 9690 |
rs149291005 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157219339 | CTCATCACCAGCTGG[C/T]AGTACGGTGCACACA | 9690 |
rs149291516 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157151156 | GCAGCAGTAGCAAAG[C/T]GTCTGTGGACATAAT | 9690 |
rs149314475 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157139400 | CCGGGGCTCGGGGCT[-/G]GGACTCGGGGCTGGA | 9690 |
rs149342160 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157216306 | CACCACTTAGAGGTA[C/T]CTTTCATTAGAACTC | 9690 |
rs149360047 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157227819 | GTTAAAAAACTGATC[A/T]CACCCACCTCCCTAG | 9690 |
rs149361418 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157157840 | ACAAAAATTAGCCAG[G/T]CATGGTGGTGGAAGC | 9690 |
rs149414977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157162024 | GCAGTGAGCCAAGAT[C/T]GCCACTACACTCCAG | 9690 |
rs149430905 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157267409 | CCTGGGCGACAGAGC[A/T]AGACTCCATCTCAAA | 9690 |
rs149432038 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201755 | TTTAATGCCAGGTTT[C/T]TGAGACATCTTTGGT | 9690 |
rs149432296 | in-del | -/TAAGAGCCTCC | 0.0418432 | 0.138458 | intron-variant | UBE3C | GRCh38.p7 | 7:157190311 | AGCATCTCTCCCTCT[-/TAAGAGCCTCC]TAAGAGCCTCCTCTT | 9690 |
rs149472708 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144684 | TGTTTGTCCAGTGCT[-/T]TTTTTTAAAAAAAAA | 9690 |
rs149473604 | snp | A/T | 0.000527235 | 0.0162277 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174970 | CTGTTTGTCAAGCAG[A/T]TGGATGGATCTGAGA | 9690 |
rs149480884 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157241986 | AGGTGGGTGAGTGAT[C/G/T]GCCAGGGCTGGGAGG | 9690 |
rs149485047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170646 | GATACACATAAAAAT[A/G]TGTATCCAAAAATAG | 9690 |
rs149486055 | in-del | -/AATTT | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157204236 | CTGAAACTGGCACTC[-/AATTT]AAGTCAAAAATAGTT | 9690 |
rs149502099 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157182563 | AGATTATTTTAATAG[A/C]GTTAACAGAGTTAAA | 9690 |
rs149550187 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157248122 | TGTCTCTTCATAATT[C/T]CACGATTTCGCTCCT | 9690 |
rs149557310 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157154396 | TCCCCTAACTTCCCA[C/T]CATTATTTTCTCAGT | 9690 |
rs149571881 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157261031 | AGACTGGCCAGGTGC[A/G]GTGGCTCACACCTGT | 9690 |
rs149573821 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157192460 | AAAGGCCAAGATCCA[A/G]GATAAGGAAGGAATT | 9690 |
rs149627920 | snp | A/G | 6.59935e-05 | 0.0057439 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207540 | GATAACGAATTCTTC[A/G]GTGATCCCATAGAAG | 9690 |
rs149657882 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157155943 | TTGTCTGTAACTGCT[A/G]CTAGGCATCCTTACG | 9690 |
rs149674101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195027 | ACTAAGAGATTCACT[C/G]TCAGGACAGCCTTCT | 9690 |
rs149724369 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157199563 | GCAACCTCAGCCTCT[C/T]AGGTTCAGGCAATTC | 9690 |
rs149740463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238815 | AGTCCAGAGAGTAGA[G/T]AATTGACTAATAGAA | 9690 |
rs149745407 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157145192 | GTTGCAGTGAGCCTG[G/T]ATTGTGCCAGCGCAT | 9690 |
rs149790696 | snp | A/G | 1.69023e-05 | 0.00290704 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182133 | TTTACAGCCTTCACA[A/G]AGGAGTTTCTGGCAG | 9690 |
rs149796654 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157209411 | CCTATTTCTGTATTC[C/T]TAAGTAAACTGGGAC | 9690 |
rs149815638 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157152468 | CAATGAGGGCCTAAA[A/G]CCTGCAGTGGGCATT | 9690 |
rs149829385 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE3C | GRCh38.p7 | 7:157256789 | CACACATGCCACGCC[A/G]TTTTAGAGAAGGGAC | 9690 |
rs149862896 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157250763 | CATTAGGAAGTACTC[A/G]ACATCCAGTGATGTC | 9690 |
rs149882925 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157230781 | CATCCCGAGCCACAT[C/T]GGCCTGTGGGCTGCA | 9690 |
rs149938317 | snp | G/T | 0.00168849 | 0.0290068 | intron-variant | UBE3C | GRCh38.p7 | 7:157163900 | TCTGTAGATAAGCAT[G/T]TTTTCTACAGCATTT | 9690 |
rs149950653 | snp | C/T | 0.000164997 | 0.00908138 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231244 | ACTAATGAAGGGCTT[C/T]TGTACCCCAACCCGG | 9690 |
rs149956149 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157174192 | ACATGGCAAACCCCG[C/T]CCCTACTAAAAATAT | 9690 |
rs150010532 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157149639 | TAACCACTTGAATGT[G/T]TGCTGATTTTCTTGA | 9690 |
rs150027479 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157183737 | ATCTAAATATGTTTC[C/G]TATTATAACACAGTT | 9690 |
rs150105960 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244903 | GCTTCTAGGAACAAG[C/T]GTGGTACAGCTGGCT | 9690 |
rs150111164 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157150968 | GGAGAGTCAGTTCTC[C/G]GCCGCTTGCGGGGCT | 9690 |
rs150128124 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157186677 | TTGACTGGATCCCTA[A/G]AGGATTTCACACTAA | 9690 |
rs150180285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157717 | TGGTAGCTCATGCCT[A/G]TAATTCTAGCACTTT | 9690 |
rs150193811 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157264001 | TGTCAGAAACTCCTG[A/G]CCTTGAGTGATCTCC | 9690 |
rs150196782 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157196154 | TTAAGATAGAAGGCC[A/G]CAAGCCAAGGAATGC | 9690 |
rs150262512 | in-del | -/CA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264306 | CCTGTTACACACACA[-/CA]CACACACACACCTGG | 9690 |
rs150266636 | snp | A/G | 0.00444435 | 0.04693 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254013 | CGCCAACCGGATTGC[A/G]TACATCCACTTGGTG | 9690 |
rs150266645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213770 | TGATATTCTAAATAA[A/G]TATTTTGGGAATTGG | 9690 |
rs150266903 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157240680 | TGTTTAGAGAGGAAA[C/T]TAATCCGTGAATGGA | 9690 |
rs150285052 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218671 | TCACAGCAAAAGAAG[C/T]AGTCCTGGCAGGGTG | 9690 |
rs150339434 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157153434 | TTTTCTTTGTTGTAT[C/T]GCGTAATGGGAGAGT | 9690 |
rs150351494 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157259333 | AGTTTCCTTTCTTCT[A/G]TACCCCCATTTTCAA | 9690 |
rs150362446 | snp | A/G | 0.000230783 | 0.0107396 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174949 | AACTTAATTAAACAC[A/G]GCTCTCTGTTTGTCA | 9690 |
rs150390788 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157192262 | TCCACCAAAGTGATT[A/C]TAAATCCCTACCACG | 9690 |
rs150407974 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157233167 | ACTATAAATTTGTGA[C/T]CTTTTGTGATTGGCT | 9690 |
rs150409893 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157139687 | CCCTTCCATGCAGGA[C/G]GCCGGTGAACCCTGG | 9690 |
rs150480887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175744 | AGGAATAAAGAACCT[A/G]TTAGAAGAGAGAACC | 9690 |
rs150512292 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE3C | GRCh38.p7 | 7:157234503 | ATTAATAGCAGATGG[A/G]AGTAGAACCGCAGCC | 9690 |
rs150564236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157238393 | ATGGAGTGTCACATC[A/G]TTCAGGTGGAGTGAT | 9690 |
rs150566414 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157144786 | CCCTCACCTCACTTT[G/T]CTCTATTACTAGCAT | 9690 |
rs150582367 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157177619 | ACACCCCTCGAGAGA[C/T]ACCAGTGTGGTGCTG | 9690 |
rs150637302 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBE3C | GRCh38.p7 | 7:157152203 | GAAGGTAGTCAGGGA[C/G]AGAGCTGGGAGGAAG | 9690 |
rs150653857 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157189154 | ATGAAAGTGAACACT[C/T]GTGTCTGAATATGCC | 9690 |
rs150656109 | snp | G/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181608 | TTCCTATAGCAAAAA[G/T]TTTGCTAGAGAATGT | 9690 |
rs150658493 | in-del | -/TG | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157157436 | AAATGATTCAAACTG[-/TG]GAAACATAAAAAGTT | 9690 |
rs150703296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194471 | AAGACTTTTCTAGGT[A/G]CTTAGAATGCTGCTG | 9690 |
rs150716906 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | UBE3C | GRCh38.p7 | 7:157264681 | CAACCTCTGCCTCCT[G/T]CCTCAGCCTCCCGAG | 9690 |
rs150771901 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157202704 | CCCTGTGCTGTAATC[A/G]GAAAAGATGAAGTGT | 9690 |
rs150792878 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157215707 | TTTTCAGAAAACGCC[A/G]TCTTGAGCTCTGTAG | 9690 |
rs150810026 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157251539 | CTTCCTCATCTCAGA[C/T]GGGTGTGAGTGCCGG | 9690 |
rs150845312 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157183403 | ATGGGGAGCTTCCAT[A/G]CCTTCTCCAGGCACT | 9690 |
rs150913410 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157230019 | ATTCAAGTGATTCTC[C/T]GGCCTCAGCCACCCA | 9690 |
rs150917448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158912 | TGGTCCATTGTGCTC[C/T]AGCACCAGAAACTAC | 9690 |
rs150924111 | in-del | -/T | 0.298467 | 0.246695 | intron-variant | UBE3C | GRCh38.p7 | 7:157144683 | ATGTTTGTCCAGTGC[-/T]TTTTTTTAAAAAAAA | 9690 |
rs150947851 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157186243 | AGCCTGACCAACATG[G/T]TGAAACCCTGTCTCT | 9690 |
rs151018797 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157232960 | GGTTTTTAATATATT[C/T]ACTGTGTTATGTGAC | 9690 |
rs151037730 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | UBE3C | GRCh38.p7 | 7:157209211 | CATCCTCCAAGTCCA[C/T]GAGAGTCTCTCTCCA | 9690 |
rs151038302 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157142182 | CTCTTTGACTGCCGC[A/G]TAAGTCCCTTCCCTT | 9690 |
rs151055426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246498 | AGTTGACTGTCTCAT[A/G]GATGAATGACTACCC | 9690 |
rs151092400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157145963 | TGGATCTTGCTTCTC[A/G]CGTTGTGTCTAAAAA | 9690 |
rs151104396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250078 | AGGGATACTGACCCT[A/G]TGTGGTGAGAACAGG | 9690 |
rs151109095 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157180086 | ATGTGTCCCAATATA[C/T]GAAATGCTTAAAAAT | 9690 |
rs151162507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153378 | AAATAGTTAACTCTG[A/G]AACCAACTGTCTGTG | 9690 |
rs151177711 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157259247 | CTTCAGGTGTTAGGC[C/T]GGTTGTCCCTTCGCG | 9690 |
rs151178625 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157190080 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 9690 |
rs151179307 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157163414 | AAAAAAAGGAAAGAA[A/G]TGATACCCAGAGACC | 9690 |
rs151231681 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157195562 | AATTTCTGCTTTTTG[A/G]ACAGGAATGTGTATA | 9690 |
rs151251169 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157171809 | CCTCACGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9690 |
rs151317181 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157217978 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTGCA | 9690 |
rs151318477 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | UBE3C | GRCh38.p7 | 7:157150176 | TGAGGTCAGGAGTTC[C/T]AGACCAGCCTGGCCA | 9690 |
rs151335042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157253711 | ATTCCCTAGTGCTTC[A/G]GAGGAAACATGGATG | 9690 |
rs180670880 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206648 | GGCTGGAGTGCAGTG[A/G]CGCAATCTCAGCTCA | 9690 |
rs180677190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181935 | AGTTATCTTAATAGA[A/G]AAGACATTAAGTTTA | 9690 |
rs180684859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221872 | TTGTGTTTTCTTGGT[G/T]GTTTTTTGTTTTTTT | 9690 |
rs180686415 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157189982 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 9690 |
rs180690575 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157153951 | TGAGTGAGCCAAGAC[C/G]GCGCCACTGCACTCC | 9690 |
rs180693769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157168643 | AAGTTCTCACATATG[C/T]TGTAACATAGGTGGA | 9690 |
rs180702112 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157174046 | ACAAGGCTATGTGGC[A/G]TATTTATGACTAGCT | 9690 |
rs180708262 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161223 | TCTGCTTAATGTAGA[A/C]GTGAGTAAGACATAT | 9690 |
rs180731271 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243788 | ACAATCCGAAAACTC[C/T]TAACACAAGAATGAA | 9690 |
rs180766176 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157229597 | GCTGGGATTACAGGC[A/C]TGTGCCACTGCACCC | 9690 |
rs180766371 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157199274 | GCTTTTTTCTTACTC[C/T]TTTTTCCGTATGACT | 9690 |
rs180790772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217103 | ATAGTAATGATAAAC[C/G]TTATTACTAACTCTT | 9690 |
rs180921758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186082 | TGAATCAAATCTTCT[A/G]GAGAGATTAAGGTAT | 9690 |
rs180928132 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149003 | CAGTTATGCTGTATC[C/T]TTTACATGTAGGAGC | 9690 |
rs180930208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157157323 | GTACACATAAAAATA[C/T]CATAACCAAGGTTAA | 9690 |
rs180958961 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157171827 | TTCTCCTGCCTCAGC[A/T]TCCCAAGTAGCTGGG | 9690 |
rs180981087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140954 | ATTGAGGAGGAAGGG[C/T]GAGAGGGAAGCTGGG | 9690 |
rs181186206 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157240216 | CCCACCACCACGCCC[A/G]GCTAATTTTTGTGTT | 9690 |
rs181189495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157213895 | AGTTATGTCCCATGC[A/G]ATATTGTGGACATAC | 9690 |
rs181194509 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262373 | AAAGAGACCTACAAA[A/G]ATCAGTAATAAGAAT | 9690 |
rs181194663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157226304 | AAGGAGAATTATACT[A/G]TGATAGCATTTGGAG | 9690 |
rs181200729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195364 | AGAAGAAACAAACTG[A/G]TAAGCTGATACTCAG | 9690 |
rs181206294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165918 | ATGGGGTTTCCTTTA[G/T]AGGTGACTAGCTGCT | 9690 |
rs181211369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177887 | CATTGAAACAGCCTC[C/T]TGGGTCCCTCATTAA | 9690 |
rs181231486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219674 | TGGGAGACCGAAGTA[C/T]GTGGATCACCTGAGG | 9690 |
rs181239682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231395 | TTATGTTTATGTGTG[A/G]TTGTTATCCAGGTTT | 9690 |
rs181244573 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157202379 | AAGTCTAAGCCGGCC[A/G]GGCGCGGTGGCTCAC | 9690 |
rs181279243 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157267461 | AGCAAATGTGGTTTC[C/G]GGAAAATGTGACTGC | 9690 |
rs181298182 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157259629 | AGCAAGACACAAGAC[G/T]ACGTATTATTATATG | 9690 |
rs181321806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236023 | TTTAATGCATATGTT[A/G]GTGATTGTTTACTGT | 9690 |
rs181367917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153417 | GTTCATCTTTTCTGG[C/G]CTTTTCTTTGTTGTA | 9690 |
rs181398630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223973 | AAATTTTTTGTGAAG[A/G]TATGCTTCTGTACAT | 9690 |
rs181406905 | snp | C/T | 0.00660683 | 0.0570944 | intron-variant | UBE3C | GRCh38.p7 | 7:157254335 | CACTGCTAGTTATTG[C/T]TTCTGAAAATGTTGC | 9690 |
rs181410913 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157233025 | ATCCCAAAAAGGAAA[C/T]GCTAGGTAGTCACTC | 9690 |
rs181415142 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216764 | GGCTCGACCTGGGTT[A/C]CTGCACCACCGCTGT | 9690 |
rs181415424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229182 | TATCTTTTCTGCAAA[C/G]CACCTGTAGAACATT | 9690 |
rs181418137 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157181190 | ATATTTGTGATGTTA[A/T]GGAACTACTCTTCAT | 9690 |
rs181422673 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157144700 | TTTTTTAAAAAAAAA[A/T]AGACTTTATTTTTTA | 9690 |
rs181425772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162966 | TTTCACTTCCTTCTA[C/T]AAACCAAGTCATTTT | 9690 |
rs181427156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198374 | AGTTTATTTCTTGAT[A/G]TGTCATCCCTTTGGC | 9690 |
rs181428674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168266 | TGAGGCAGGAGAATG[G/T]TGTGAACCCAGGAGG | 9690 |
rs181431157 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157247650 | TGAGCTGAGATCGCG[C/T]GGCTGCACTCCAGCC | 9690 |
rs181434047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202938 | TTTTTGGTGGGTTGG[A/G]GTGGTATATCTAAAA | 9690 |
rs181435116 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157174825 | GGTTTGATTAAATGT[A/G]CATTGCCACTAAAGG | 9690 |
rs181441771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220432 | TATGTTTAGATATTA[G/T]GCACCATCAAATAAA | 9690 |
rs181449007 | snp | C/T | 0.000803894 | 0.0200325 | intron-variant | UBE3C | GRCh38.p7 | 7:157187069 | GCCAGCCAGAGAACA[C/T]ACCTTCCTCCCTGGG | 9690 |
rs181460919 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148432 | TTTAATTCCTCCCCT[A/G]TGATAGGTCTAGACT | 9690 |
rs181463692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165291 | CGTTTCCCATATTTC[C/T]CTCATGTGCTTTTCT | 9690 |
rs181472246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194699 | CTAAATCATCATGAA[C/T]AGACTGTTGGTAGAA | 9690 |
rs181473631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172630 | CAGTCTAGAGAGGCA[A/G]TGAAAGCCGTTGAAT | 9690 |
rs181518610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157256319 | AGCGAATTTTTGTAC[A/G]TTTGGTAGAGACAGG | 9690 |
rs181533568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225914 | CTCTGATTGTGCTAC[C/T]GCTCAGGCCTTGGCA | 9690 |
rs181559527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190947 | GTCTCTTCCAGTTAA[A/T]GTCTGGGCTGGCATG | 9690 |
rs181646809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265049 | GTTTTTTAGTTGTTT[A/G]CAGCTCTTCCTTCGT | 9690 |
rs181698194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212533 | CATTGCCATGAACTC[G/T]CAAACATAGCGATCT | 9690 |
rs181704164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157239737 | TGCTGGAAATAAGTC[A/G]GTGGAATTGCTGAGG | 9690 |
rs181767428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157162383 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 9690 |
rs181801251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235728 | AAACTAAGAGTAATT[G/T]GAGGATGGTAGTTAA | 9690 |
rs181808852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223774 | AGAATACAAAAGTTA[A/G]TTGGGCGTGGTGGCA | 9690 |
rs181813733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253770 | GCTGGGCTTCGGAGA[C/G]TCTTCCTGGAGGTGC | 9690 |
rs181826819 | snp | A/G | 1.65488e-05 | 0.00287647 | intron-variant | UBE3C | GRCh38.p7 | 7:157207572 | TAAGGATTTTGAGAA[A/G]CCAGTTTGCTGCTGG | 9690 |
rs181860592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157267244 | CTGGCCAACGTGGTG[A/G]AACCCCTTATCTAGG | 9690 |
rs181925855 | snp | C/G | 0.000115305 | 0.00759205 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256969 | GAGAGTTGTGGAAGG[C/G]TTCACTGATGAAGAA | 9690 |
rs182000774 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217535 | TTCAGTAGTATGATA[A/C/T]GTTAGTAAAAAATTT | 9690 |
rs182009769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157186761 | GAAAAATGTGATTTC[A/G]TATATGTTTGTAGTG | 9690 |
rs182019154 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157202695 | TGCCAATCCCCCTGT[G/T]CTGTAATCGGAAAAG | 9690 |
rs182022267 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157172491 | TTACAGCGGACAAAG[C/G]AATACATGATTATTC | 9690 |
rs182035696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141503 | CAGCCCGTTGCCCCT[A/G]TGCTACACACCTGGA | 9690 |
rs182037240 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157157880 | CAGCTACTTGGAGGC[C/T]GAGGCAGGAGAATTG | 9690 |
rs182041920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190360 | AACAGGCCCGTCATC[A/T]ACTTGGTTGTCTGTA | 9690 |
rs182044263 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144385 | GAAATTCGGTGTCTC[A/G]GAAATAGTTTTGTCT | 9690 |
rs182079557 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157244046 | GACAATCCTGGCCAA[C/T]GTGGGGAAACCCTGT | 9690 |
rs182101188 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157145712 | TTTAAGGCTCTTTTC[A/G]TGGCTTGACAGTTCA | 9690 |
rs182134711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224288 | CAACCTCCGCCTCCC[A/G]GATTCAAGCGATTCT | 9690 |
rs182147247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209231 | GTCTCTCTCCAGCCC[A/G]TTCTGCCTGGTTTTA | 9690 |
rs182148495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157237027 | GTGAGCCAGCACACC[C/T]GGCAAGACAGTTTTC | 9690 |
rs182158631 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157232703 | TTGCTATTGTGATTA[A/C]TTTCTGTAAGAATCA | 9690 |
rs182161397 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263237 | AACACCACCTTCCCC[A/G]GGCACCTGTCCTAAC | 9690 |
rs182162258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191210 | ATTTAGATAAACAGC[A/G]GTGCGCCTCGAAGCG | 9690 |
rs182166882 | snp | G/T | 0.147656 | 0.228091 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139213 | CCCAGCCCGCCCCGT[G/T]CCCCGCCCGCCCGGC | 9690 |
rs182170967 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163157 | TTGGGAGGCCGAGGC[A/G]GGTGGATCAGGAGGT | 9690 |
rs182171073 | snp | A/C/G | 0.000961392 | 0.021904 | intron-variant | UBE3C | GRCh38.p7 | 7:157175061 | TTGTAAGTCAGTAAC[A/C/G]TATATAATGTATTGA | 9690 |
rs182237629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147663 | TTCTCATCATGAAGT[A/G]TGATGTTTGGTGGGT | 9690 |
rs182286166 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157260952 | GCCACTTGTGCTGCG[G/T]GAGCGTCGTAGGTTT | 9690 |
rs182325628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174344 | TCTGATATTTGCAAG[A/T]GAACTATTTTTGTTT | 9690 |
rs182385461 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157229958 | CTGTCACGCAGGTTG[A/G]GATGCAGTGGCACGA | 9690 |
rs182396013 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157260181 | TTACCAGATATGGGG[A/G]GTGGGGGTGGGAAGT | 9690 |
rs182414915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157200956 | TAGATTTATTTTTGA[A/G]ATGTTAACAGCACAT | 9690 |
rs182421050 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157247434 | GGATGGCTCACACCT[A/C]TAATCCCAGCACTCT | 9690 |
rs182438306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157170211 | TTGTCAATTTCCACC[A/G]TTCCTGTAAACACAG | 9690 |
rs182445295 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157166985 | CCCAGGCTGGAGTGC[A/T]GTGACATGATCTCAG | 9690 |
rs182485533 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157241174 | CTGAGGATCACAGAG[C/T]GCTGCAGGGCATGTG | 9690 |
rs182490430 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157228093 | ATCAACTAATGTGAT[A/G/T]ATTCCACGTGTCATC | 9690 |
rs182494595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157257945 | TCTTTTTTCCTTTTT[C/T]CTTTTTTTTTTTTTT | 9690 |
rs182499029 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157164882 | GCCTATATTAGAGAT[A/G]GTGTTTAGGGGAAGG | 9690 |
rs182511042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215480 | ATAAATTTATATATT[A/G]TATATACTAGATACA | 9690 |
rs182516831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179188 | CCTGACCAGGAAGGG[C/T]TCTTACCACCTCCTG | 9690 |
rs182527202 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157196836 | GAGCTGGGCGTGGTG[A/G]TGCATGCCTGTAATC | 9690 |
rs182532601 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157230128 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 9690 |
rs182541390 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157260749 | TCAAAACACTGGAAG[A/T]TGCAGAGACTTTTGT | 9690 |
rs182545800 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157244762 | AATTAATCCTTTTTA[G/T]TTCAAATCATTTTGG | 9690 |
rs182562216 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157217835 | AGAGCGAAATTCCGT[C/T]TCAAAAAAAGAAAGA | 9690 |
rs182563624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157183016 | CTTCCCACAGTGCTG[A/G]GATTACAGGCTTGAG | 9690 |
rs182568737 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157220202 | GGTGACAGAGTGAGA[C/T]CGTGTATCAAAAAAT | 9690 |
rs182622771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142456 | ATAGAGTAATTGCTA[C/T]ATTCTAAATTTCCCT | 9690 |
rs182681920 | snp | A/G | 1.67832e-05 | 0.00289677 | intron-variant | UBE3C | GRCh38.p7 | 7:157183844 | AAAAAATAATGTTTA[A/G]CTAAAATACGTTTTA | 9690 |
rs182689539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155892 | CAGGACGATGGCCTC[A/G]GTCGTTTCAGAGACC | 9690 |
rs182698755 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157230435 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9690 |
rs182708297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157254607 | TTTGCCATGTTGGCC[A/G]GGCTGGTTTCAAACT | 9690 |
rs182777971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157166752 | AAAAAAAAAAAAATC[A/G]ATATTTTGAATTATT | 9690 |
rs182779627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178336 | ACTGTTAAAGAGATT[C/T]GTATCTGAGTTTAAT | 9690 |
rs182786196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150832 | TAGTTGCTTATTGCT[A/G]TGTAATAGAGCTTAA | 9690 |
rs182907545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187960 | CTTTGAAATAAACTT[C/T]TGGTTCAGACAAAAC | 9690 |
rs182919933 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157158798 | AATTAGAAGAAATGC[A/T]TTAAAATCTATTGTT | 9690 |
rs182930468 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137153 | CTGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 9690 |
rs182981600 | snp | A/G | 0.000330338 | 0.0128476 | intron-variant | UBE3C | GRCh38.p7 | 7:157220684 | ACCAGGATTGCCCCC[A/G]ACAGGTCACTCAGCT | 9690 |
rs182985758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248864 | TTGCTGCTTGTCTGG[C/T]TCTTCCCGGTGCTGG | 9690 |
rs182986963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218063 | TGTTAACAGAGGGAC[A/G]TAAGGTATTTTCAGT | 9690 |
rs182992357 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157245891 | AGCTACTCAGGAAAC[C/T]GAGACAGGAGAATCG | 9690 |
rs182996339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267897 | CATTCCTCCCTCCCT[C/T]CCTTTTTTAAATGAT | 9690 |
rs183024508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210766 | GACAGAATTGCAAAC[A/G]ATGAGACCTGACTCC | 9690 |
rs183090091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157237978 | GATTGCTTGAGCCTG[A/G]AATGTAGAGGCTGCA | 9690 |
rs183131428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252449 | AAGCCCATTCTTAGG[C/G]TTGATGGTTCCAAAC | 9690 |
rs183140901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265888 | CATCTGAAAAACAAT[A/C]TTCAAATTTCCCTGA | 9690 |
rs183169845 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157199575 | TCTCAGGTTCAGGCA[A/G]TTCTCCTGCCTCAGC | 9690 |
rs183174666 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157169806 | CTGCCCCAGCCTCCT[C/G]AGTAGCTGGGACTAC | 9690 |
rs183180910 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157182624 | TTCCCTCCCTCTGCT[A/G]AATTTCCAGTGTGCC | 9690 |
rs183181407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204996 | GTTAGGGATTGCCTC[A/G]GGTCTCACTGATGGT | 9690 |
rs183188862 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157172910 | TTAGTCATCAGTCAC[A/G]ACATGGTGTAGCTAC | 9690 |
rs183190704 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157151721 | ATTTAGCTTTTTAAT[C/G]CATTTGCCCTTGGAG | 9690 |
rs183191451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154479 | TTAAAATGAGAGATC[A/G]TATTGCTTTTTCACC | 9690 |
rs183197486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155130 | AAATTGGCGGTTCTC[A/G]TATTTTCATAGAGAT | 9690 |
rs183235939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265283 | CAGGCTGCGACAGTG[A/C]GCAGACTGAGGGCGA | 9690 |
rs183248588 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157141724 | TTCTGACCTCCATTA[A/C]TGTAGATGAGCGTTA | 9690 |
rs183275483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233254 | CTCATTTGAAGGGCC[A/G]AATCTTATTTCATTG | 9690 |
rs183289988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224697 | TTTTTAGGCCTATAC[A/G]CTCTATTTGCATGGT | 9690 |
rs183291550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157193758 | TGACTGACCTCACAC[A/G]TGGTTGTCTGTTCAT | 9690 |
rs183303403 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157196711 | CAGTGGCTCACGCCT[A/T]TAATCCCAGCACTTT | 9690 |
rs183327271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254855 | AACCAGCCTGGGCAA[C/T]GTGGCGAAATCCCAT | 9690 |
rs183346036 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269103 | TTGAATAATAAATTA[A/G]GCGTTTAAATGCTAT | 9690 |
rs183359462 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157237800 | CCTGTAGTCCCAGCA[C/T]TTTGGGAGGCCGAGG | 9690 |
rs183365922 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157254933 | GCGTGGTGGCGTACA[C/T]CTGCAGTCCCGGCGT | 9690 |
rs183366794 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157224541 | ATATCTTAATTCCTT[G/T]TCTGGTGTCTTTGAT | 9690 |
rs183372981 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157221411 | GCCTCTGTTGTTCCC[A/G]GTCCTCATCAGCACT | 9690 |
rs183379530 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157240351 | TGAGCCATAGCACCC[A/G]GCCAGCAAGCTGTGA | 9690 |
rs183381683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157205214 | GTCTGCAGGGCAGCA[C/T]TGGCACATATCCTTG | 9690 |
rs183388478 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196838 | GCTGGGCGTGGTGGT[A/G]CATGCCTGTAATCCC | 9690 |
rs183390222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157233585 | ACACCCAGTCACCGC[A/G]TTTTGTTTACTTACT | 9690 |
rs183395849 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188243 | TCTCTTTGTTTTTAT[A/G]AAATGCCATCCCATC | 9690 |
rs183409265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226513 | ATTAAAAATGAAATC[A/C]TCTTACCCAGCTTTT | 9690 |
rs183411009 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173291 | TGAGGCAGGAGGATC[A/G]TTTGAGCCCAGGTAT | 9690 |
rs183428689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157170140 | TTTTTTTTTTCTTTT[C/T]AACCATTTTTTTTCT | 9690 |
rs183436466 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138333 | GTATTGATGCTGTAT[C/T]TATAGATGCATATGT | 9690 |
rs183467785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158324 | ACATGCCAAATTCCA[G/T]TGTGAAACCATGCAC | 9690 |
rs183497289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164661 | TGCTTTTTTAGGTAG[A/G]GTTTTTTGTTTTGTT | 9690 |
rs183504571 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157176524 | AGGTCATCCGCCTGC[C/T]TTGGCCTCCCAAAGT | 9690 |
rs183508638 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157215153 | TTTGATCTTGAGTGG[C/G]TTTTTACTATGCAGT | 9690 |
rs183535974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159703 | TGAAACCTTGTCTCT[A/G]CTAAAAATACAGAAA | 9690 |
rs183537742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142831 | CGTGCATAGGTACCC[C/G]CTAACTCTAAAATAA | 9690 |
rs183587069 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157257588 | AAAAATACAGAAAAA[C/T]GAGCCAGGCATGGTG | 9690 |
rs183703526 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157264665 | GTCTCACTGCAGCCT[A/G/T]CAACCTCTGCCTCCT | 9690 |
rs183724532 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157225076 | CCTGAGTGCAGTGGC[A/G]CCTGCAACCTCTGCC | 9690 |
rs183732528 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255267 | GAAAAATGCCACTTA[C/T]ATCCAAATGAGATAA | 9690 |
rs183737907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211659 | GGTAACTAAGGGCTA[A/T]ATAAAATTTGGTTAA | 9690 |
rs183748737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194147 | TTGACCCATGAAAAA[G/T]TTGTTTTACCCCTGG | 9690 |
rs183783238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192574 | TTACTCTTCATCTTG[C/T]GTTGAGACTTCGTGG | 9690 |
rs183786196 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163558 | GTTTTACCTGTACTC[A/G]TTTGTATATGTGAAG | 9690 |
rs183795349 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157240669 | TGAATCTAGGCTGTT[C/T]AGAGAGGAAATTAAT | 9690 |
rs183895503 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143375 | AAAAACAAGTTTATG[A/G]AAGGATAGGCGTGTC | 9690 |
rs183931127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214778 | AGATTTCATCTTTGC[G/T]TTTGAAGAGTAAAAT | 9690 |
rs183961966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175379 | TTCCATTCCATAGGG[G/T]TCTCCACCAAAATGC | 9690 |
rs183962753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265626 | ATAGCCTCACCATTA[A/G]TAGGCAAGATGAGCG | 9690 |
rs183979399 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157259630 | GCAAGACACAAGACT[A/G/T]CGTATTATTATATGT | 9690 |
rs183982995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242738 | CCTGAACCTGGAAGC[C/G]ATAGAACTAGAAGTC | 9690 |
rs183985181 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157161006 | ATTGAGGGACAGCAT[C/G]CAGGACATGAAAGAT | 9690 |
rs183985470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157146299 | CAGGCTGGAGTGCAG[C/T]GGCGCAATCTCGGCT | 9690 |
rs184010367 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | UBE3C | GRCh38.p7 | 7:157229546 | GGTCTCAAACTCCTG[A/C]CCTCAGGTGACCCAC | 9690 |
rs184020437 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157175795 | TAATTCATATTTTTT[C/T]TAACTTATTTCTTTA | 9690 |
rs184026638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164404 | CATGCAATCGCCTCC[C/T]TCATTTTCCCAAAGT | 9690 |
rs184028214 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147010 | TCTTCTTTAGTATTG[G/T]GTTGGCTATTGTGGA | 9690 |
rs184047862 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157209507 | TAAAAAATAAGCAGT[A/C]TCACCTATTTAAAAC | 9690 |
rs184050374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178009 | AATCTAAAAATAAGT[A/T]CGGTGTTAGACAAAG | 9690 |
rs184080738 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE3C | GRCh38.p7 | 7:157149316 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 9690 |
rs184092169 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157195935 | AAACGTTAATGTCCT[A/C]ATCTCCAAACCTGTA | 9690 |
rs184126315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157251732 | AATTTTAAATATGTC[C/T]CTCAGATCTGAAATT | 9690 |
rs184178121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147418 | CTTAGTTCCAGGAGT[A/G]GTTTTTTGGTTGATA | 9690 |
rs184223944 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166474 | GGCTGGGCGCGATGG[A/C]TCACGCCTGTATTCT | 9690 |
rs184228795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246912 | CTCTTTTTTTGAGAC[A/G]GAGTTTTTGCTCTTG | 9690 |
rs184239807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157262295 | AGAAAAAAAAAGACA[A/G]TGGATTTTAGCACAT | 9690 |
rs184247786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219516 | ACAGGAAACATAGGG[G/T]TTAGAAGTACATCTT | 9690 |
rs184258819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202341 | TAGCCTAGTACTCTG[C/T]TGTTGAATTTTTCCT | 9690 |
rs184260135 | snp | A/G | 1.67139e-05 | 0.00289079 | intron-variant | UBE3C | GRCh38.p7 | 7:157231359 | ATAAAAATAGACCTC[A/G]GACCAAAAGATGTTG | 9690 |
rs184402631 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157152606 | TCTCGACTTCTGATA[C/T]GTGAGGCAGAGGTGT | 9690 |
rs184465219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231961 | AATTTATTATTTGAC[A/T]GTTCTGGAGGCTGGA | 9690 |
rs184469955 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202422 | AGCACTTTGGGAGGC[C/T]GAGGCCAGCGGATCA | 9690 |
rs184545478 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157262656 | GAACTCCTGACCTCC[A/G]GTGATCCACCCACCT | 9690 |
rs184557066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256020 | AGCCCCTTCTCTGCC[A/G]TCTGTTCAGCGGCGG | 9690 |
rs184561843 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157239272 | TTACTGAATGAACAG[A/G]CTACAGCTACTCAAA | 9690 |
rs184577566 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157253260 | CTTGTCTGTCATACA[A/C]GTGGGGGACAGTAAG | 9690 |
rs184602292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220028 | CCAGTCTGGGCAAGA[C/T]AGCAAAACCCCATCT | 9690 |
rs184614975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186350 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 9690 |
rs184647790 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157216437 | CGGAGTTTGTTGTAC[A/G/T]CATCCTTAGATCACT | 9690 |
rs184661600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157198213 | ATATATTCAGACCGC[G/T]TACAAAAGGAATTAC | 9690 |
rs184662508 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157247347 | AGTGCCTGGCACCTA[C/G]TACCTAGTAAGTGCT | 9690 |
rs184667478 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157233980 | TGTGCTTCATGACTT[C/T]TGTTGAGAAATGTCT | 9690 |
rs184672467 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157167495 | AAGTGATGCTCACCT[A/G]TAAGATGACTGTGCA | 9690 |
rs184672717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157206470 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTCGA | 9690 |
rs184677412 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157180954 | CCTAAAGCCCACCCC[A/G]GGGCCCCAGGTGGAG | 9690 |
rs184677748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221546 | AGGAGTTCAAGACCA[C/G]CCTGACCAACATAGT | 9690 |
rs184713202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189650 | TATTTCACATTCCTC[A/G]TCCTTCCTTTTCCTG | 9690 |
rs184714951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157161723 | CCTTCCAAAGTGCTC[A/G]GATTATAGCCATGAG | 9690 |
rs184716205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174168 | AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGC | 9690 |
rs184718929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234699 | ACTTCACTACCGTAA[C/T]GGTATGTGTTATATC | 9690 |
rs184719179 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157266300 | GCCTGGGTGACAGAG[C/G]AAGACTCCGTCTCAA | 9690 |
rs184721857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221847 | TCTTTTTCATGAATT[C/T]GTTTTTTTGTTGTGT | 9690 |
rs184730579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144155 | GGCCGAACACAGGCC[A/G]GATGCTGTGGCGCAC | 9690 |
rs184755752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157235258 | TTTCTGTTAAAGTGA[A/G]CCCAAGAACCTTCTA | 9690 |
rs184759502 | snp | A/G/T | 0.00637159 | 0.0561118 | intron-variant | UBE3C | GRCh38.p7 | 7:157258872 | ATAACTTCTAAACCC[A/G/T]CACTGACCAATTGTT | 9690 |
rs184768210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253400 | AAAAAGTGTTCTTAC[C/T]CACTCTGTTTATATA | 9690 |
rs184769977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206924 | TTGAGGTTCCAGTTT[A/G]GCTTCAATATTGAAT | 9690 |
rs184778996 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157222576 | AGGCGCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 9690 |
rs184779682 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157185502 | CATTTGGGCTGAGAA[C/G]TAAAGACCCCATTTT | 9690 |
rs184781059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190307 | AGTCCAGCATCTCTC[A/C]CTCTTAAGAGCCTCC | 9690 |
rs184787524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157156990 | ATAAGAGTCTTCATC[A/G]TTAGACTTTTTAAAT | 9690 |
rs184820877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140040 | GTTTAGGATAAGGGT[A/G]GGCAAACCATGACGC | 9690 |
rs184825772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157156527 | GGCTGGGCTGGTCTT[A/G]AACTCCTAACCTCAA | 9690 |
rs184858235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206605 | ATATTTTAAACTTCT[C/T]TGAAACAGAGTCTGG | 9690 |
rs184861299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173920 | CCCAGTTTAAGACAT[A/G]CGCTAATTTATTATG | 9690 |
rs184871377 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219249 | CCAGAAAGTTGTGCG[A/T]TGGGAAAATGTCAGC | 9690 |
rs184892454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184665 | ATTGATTACTACTAA[C/G]TGTAATCACAGAATA | 9690 |
rs184900514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157202069 | GCCATGTTTTTAAAA[A/G]AGCAGACATTTGGAA | 9690 |
rs184904565 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157171445 | AGGGTCTCATGTTTT[A/T]AAAAAAAATCCCAAA | 9690 |
rs184905925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170950 | TAGCTGGGACTACAG[A/G]TGTGTGTACACCTTG | 9690 |
rs184920793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157140697 | CCATTTACACAGCGC[C/T]GCGCGGCCTCTGTTG | 9690 |
rs184934019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140988 | GGAAGGAAAAGGCGT[C/T]TCAGCTGGAGGCTAG | 9690 |
rs185027766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173413 | TAAATTAATCTTAAC[A/G]TAGGGGAAAATGTCT | 9690 |
rs185049610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157143041 | TCTGGCTAATTTTGT[A/G]TTTTTAGTAGAGATG | 9690 |
rs185138073 | snp | A/C | 8.18565e-05 | 0.006397 | intron-variant | UBE3C | GRCh38.p7 | 7:157188946 | TTTAACACTGATTGT[A/C]AGGGTGTACAAATGA | 9690 |
rs185146776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157160321 | CTCAGGCGATCTGCC[A/G]GCCTTGGCCTCCCAA | 9690 |
rs185208098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157457 | CATAAAAAGTTAGAC[A/G]CTGCACTGTGCAGGT | 9690 |
rs185226237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254643 | GCTCAAGTGATCCAC[C/G]CCCCTCAGCCTCCCC | 9690 |
rs185237066 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268129 | CACTCCAGGGTTCAG[A/T]CAGGGCTGCACAGGC | 9690 |
rs185257340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209268 | ATTTCTCTTAGGAGC[A/G]TGAGCATTAGCAGCA | 9690 |
rs185263875 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157224443 | TCGTGATCTGCCTGC[C/G]CCAGCCTCCCAAAGT | 9690 |
rs185292452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157228862 | ACTATTTACACTCCA[A/G]GTACGGTAACTTCAA | 9690 |
rs185350832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259380 | ATCTTGAGAATGTTC[A/G]TCAATGTGATGTCGC | 9690 |
rs185398582 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225419 | TAGATCTTTCAGAGG[C/T]TGATTTATGCAGATA | 9690 |
rs185403541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242304 | TGAGCTGTTGTTAGG[A/G]AAACATAGTACCTGA | 9690 |
rs185423030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195517 | CTGGTTTTGTAAATT[A/G]ATGGTGCTGATGGCT | 9690 |
rs185498278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157240251 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 9690 |
rs185503186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214219 | GGAAATATGAAAGAG[A/G]ATACACTATATTGAA | 9690 |
rs185505525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157226374 | CAGTCTTGAAAGTTC[A/G]TGTGCTATTAACCTC | 9690 |
rs185508619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157194559 | GAAGAATTCTGAGGC[A/G]CATGCCAGAAAGAAG | 9690 |
rs185517455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157261408 | ATAATTGAGTTATAC[C/T]GTGGAAAACACTTTG | 9690 |
rs185520339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157246706 | GCCGTCCCTCATTCT[A/C]GGGCAAAAATTCCAG | 9690 |
rs185532919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190971 | TGGCATGTTCTCAGG[G/T]GCTTGGCTCTTTTAC | 9690 |
rs185540698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164946 | GGCAGGATTTTCCAA[C/T]CTTGGTGCTGACATT | 9690 |
rs185545296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157198552 | TTTTTTTATTTTTTT[C/T]GACAGGGAGTCTTGT | 9690 |
rs185553208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216775 | GGTTCCTGCACCACC[A/G]CTGTGTGCTCCTCCT | 9690 |
rs185553405 | snp | C/T | 0.000393199 | 0.0140159 | intron-variant | UBE3C | GRCh38.p7 | 7:157174871 | TGTAAATTAGCAAAC[C/T]ATTAAATTTTCATTG | 9690 |
rs185566352 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216054 | TGATGACATAGTGAA[A/G]TGTGTCCAGGCCAGC | 9690 |
rs185576842 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157179895 | GGGAAACAGTATTCC[A/G]AGTTAATTAAAAGTA | 9690 |
rs185583968 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157152180 | AAAGTGGAAGAGAAG[G/T]CTGGGAGGAAGGTAG | 9690 |
rs185620423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267151 | AATGTGGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 9690 |
rs185647048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212371 | GGTTGCAATACTATA[G/T]CTAAATATCCGTCAT | 9690 |
rs185647653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157241594 | GAGGAATCAGTCCTC[A/G]TGCATTGCCAATGGG | 9690 |
rs185651102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177067 | TCATGGAATCACTGG[A/G]TCACATAGTAGTTAT | 9690 |
rs185660328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181275 | TAATTATATCTTAGA[C/G]TTCCTTCCAAATGAG | 9690 |
rs185661033 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157230918 | TGACGGAGCAAGACT[C/G]TGTCTCAAAAAATAA | 9690 |
rs185662514 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157144855 | CAATGTCGATGTGTT[A/G]TTATTAATTGAAGTC | 9690 |
rs185664375 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157163029 | TTTTCATCAAAGAAA[C/T]TGATTTCTTCATTGA | 9690 |
rs185682636 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147979 | ATCTCTTTTGATGAG[A/G]GACATCAATTTAGGG | 9690 |
rs185687996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197348 | AACAAACTGATTTGC[C/G]TACAAATCCAAAAAC | 9690 |
rs185704543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148852 | ACTCCTGATCTCCAG[C/T]GATTCTCCTGCCTCA | 9690 |
rs185718865 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157167305 | TGTTCTTGAATCCCA[C/G]AGTGTGTGTGTTAGT | 9690 |
rs185764133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157228526 | TGTTGGTTGGTTACT[C/T]TTATTTTATTTCATT | 9690 |
rs185775573 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE3C | GRCh38.p7 | 7:157265106 | AAATTATCATGTGCA[C/T]CTCTAATTATTTCTT | 9690 |
rs185777828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157194771 | CTTGTTACATAGTGG[C/T]AAAAAGCTAAGCTGA | 9690 |
rs185791860 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165423 | TTTTTTTTGAGGTGG[A/G]GTCTCACTTTGTCAA | 9690 |
rs185795658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233146 | GTGGAATCATTTGTT[A/G]TATCAACTATAAATT | 9690 |
rs185798240 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157177532 | GGTTGACAAGAGGCT[C/T]TCCCACCGCCCGCCG | 9690 |
rs185805285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157220482 | GGGCATATTAGAAAA[C/T]ATAGTTAACTGTAAA | 9690 |
rs185815157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248115 | AAGGATCTGTCTCTT[C/T]ATAATTCCACGATTT | 9690 |
rs185882598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157243826 | TTTTGCAAACAGATT[A/C]ATGAATGCAGAATTC | 9690 |
rs185965472 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157169930 | CTCAGGTGATCCACC[C/T]ACCTCGGCCTCTCAA | 9690 |
rs185983109 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157265367 | AATGTGAGGCAAATA[C/G]CTAATGGTGTTTGTG | 9690 |
rs185985641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154699 | AGAAAGTCTCTTGGC[A/G]TATATTGTGATATTT | 9690 |
rs185994864 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137270 | TGAGACAGAGTCTCA[A/C]TCTGTCACCCAGGCT | 9690 |
rs186021994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157267400 | GCCCTCCAGCCTGGG[C/T]GACAGAGCTAGACTC | 9690 |
rs186022155 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157229971 | TGGGATGCAGTGGCA[C/T]GATCTTGGCTTACTG | 9690 |
rs186029318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259977 | GCCTAAGTGCAGTGA[A/G]TTTGTTTCAAATAGG | 9690 |
rs186038410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157235755 | TTAACTTAGTTTCAC[A/G]TATTTAAGACTTCCC | 9690 |
rs186042589 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157217694 | ATACAAAAATCAGCC[A/G]GGCGTGGTGGCAGAC | 9690 |
rs186050489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157253817 | AATGCTGTGCATACT[C/T]GGGTACTATTTCGTA | 9690 |
rs186050818 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157182835 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 9690 |
rs186070975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232841 | ATTGAAAAATCAGTG[C/T]CTGCAAAACAGGTGG | 9690 |
rs186082060 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157171959 | TGATCCACCTGCCTC[A/G]GCCACCCATAGTGCT | 9690 |
rs186087888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157149116 | GGCTGGAGTGCAATG[A/G]CTCAATCTCGGCTCA | 9690 |
rs186101359 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157220209 | GAGTGAGACCGTGTA[A/T]CAAAAAATAAAAAAT | 9690 |
rs186103427 | snp | A/G | 9.90949e-05 | 0.0070383 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186896 | GAAGCTGGACACAAA[A/G]CAGCAGACCAACACC | 9690 |
rs186109377 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202795 | GTAGTGATAATAGCA[G/T]TCACTGTTACTGACT | 9690 |
rs186156599 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223995 | TCTGTACATTCACGT[C/T]TATTTATCAGAAACG | 9690 |
rs186199971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166017 | ATCGTTGAGTCTGCT[A/G]TATGTAGGTGTCTAA | 9690 |
rs186217429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172541 | AACCCAGCATTGCCT[C/G]CAGAGTTGAGCTAAG | 9690 |
rs186228289 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157141681 | CATTATGCCATGTAT[G/T]TCTGTAGCCCCACAA | 9690 |
rs186237019 | snp | C/G | 0.000433084 | 0.014709 | intron-variant | UBE3C | GRCh38.p7 | 7:157254353 | CTGAAAATGTTGCAG[C/G]TGGTCATATTTCCAA | 9690 |
rs186250694 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157249369 | TGCCCAGGCTGGAGT[A/G]CAGTGGCGCAATCTC | 9690 |
rs186320166 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157236812 | TCTTGGCTCACTGCA[A/T]CCTCCACCTCCCGGG | 9690 |
rs186323742 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157168367 | GGTCCTACTATGCTG[A/G]TGAGATTGTAAAATG | 9690 |
rs186339981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157208356 | GCTGGGATTATAGGC[A/G]TGAGCCACTGCAGCT | 9690 |
rs186354708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157257144 | CTTTTACATACACTT[C/T]TGTTTTTATCTTCAG | 9690 |
rs186388598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267464 | AAATGTGGTTTCGGG[A/T]AAATGTGACTGCAAT | 9690 |
rs186406769 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157212889 | CGGCCTCCTGAGTAG[C/G]TGGGACTACAGGCAT | 9690 |
rs186408148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240158 | CCTCCTGGTTCAAGC[A/G]ATTCTCGTGCCTCAG | 9690 |
rs186435697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187351 | TACATATCTTTTTAG[A/G]CTTTTTTCATAGTAC | 9690 |
rs186447172 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157158454 | TGTAGAGAACACTGC[A/G]TCTGTGCGTTGTATT | 9690 |
rs186525981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153449 | TGCGTAATGGGAGAG[G/T]CACAATTCTCTTTCT | 9690 |
rs186608458 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224474 | GCTGAAATTACAGGC[A/G]TGAGCCACCGCGCCC | 9690 |
rs186611764 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157226017 | TCTAAAATTGACAGT[C/T]ACTACAACAGAAGCC | 9690 |
rs186611926 | snp | A/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203689 | ACTATTTTATGATAG[A/G/T]GTAGTTTTACAAATC | 9690 |
rs186649426 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172840 | GGCAGGTGCTGTGAG[A/G]TGTCGATTGGTGTCT | 9690 |
rs186683875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157228141 | CCATGCTTTACGATG[C/T]TCGTTGTCTTATCTC | 9690 |
rs186691116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258414 | AGGGGGAAAAAGTAA[C/T]GTTAAGGTTTTTTGC | 9690 |
rs186794680 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157215612 | GTATATTATAAATCA[C/G]ATTGTCCTGATTTTG | 9690 |
rs186806606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196916 | GGAGGTTGTGGTGAG[C/T]GGAGATAGCGCCATT | 9690 |
rs186831120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164434 | TGTTGGGATTACAGG[C/T]GTGAACTGCCTCGTC | 9690 |
rs186837423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176195 | GAAGCCCAGGAGTTC[A/G]AGGCTGCAGTGAGCT | 9690 |
rs186838467 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217995 | GCCACTGCACTGCAG[C/T]CTGGGTGACAGAGCG | 9690 |
rs186845185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157147172 | ATCCATGAATATGGA[A/G]TATCTCTTAATTTGT | 9690 |
rs186880015 | snp | G/T | 1.65921e-05 | 0.00288024 | intron-variant | UBE3C | GRCh38.p7 | 7:157207586 | AACCAGTTTGCTGCT[G/T]GCCACTTGGCCCATC | 9690 |
rs186893589 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157211445 | TGGATGCTATATGCA[G/T]TAATTTTATAGTGTT | 9690 |
rs186894653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157174369 | TTGTTTCAGATTGAC[A/G]TGAGCTTTAAGTGTA | 9690 |
rs186896752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230331 | CTTCCCTGAACCACA[G/T]TGGAAGAGGAATAAT | 9690 |
rs186897336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256323 | AATTTTTGTACATTT[G/T]GTAGAGACAGGGTTT | 9690 |
rs186900567 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157158975 | AAACACAGTCCTACT[A/T]GTCTCATGTATGCGG | 9690 |
rs186905401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193772 | CATGGTTGTCTGTTC[A/T]TTGTGACATCTTTTT | 9690 |
rs186905600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260782 | GCTCCTGGCTAATTA[C/G]ATAATGCTAATCATG | 9690 |
rs186907731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244767 | ATCCTTTTTATTTCA[A/C]ATCATTTTGGCACAA | 9690 |
rs186908915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142495 | ATTCAGAAAAAGTAG[A/T]ATTGTTTGGAGCTTA | 9690 |
rs186919890 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157144414 | CTGTTTTGGGAGACG[A/G]GGGAAACTTAAGTTT | 9690 |
rs186943821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260371 | AAGGGTTTAGTGGCA[C/T]GTCCAGGTTCGTGTG | 9690 |
rs186972189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157173132 | TAATACCAACACTTT[G/T]TGGGGCTGAGGTGGG | 9690 |
rs186993368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157196229 | CCTATGCAACGCTGC[C/T]GACAAACTGATGTTA | 9690 |
rs186997134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226976 | GTCCCACAGTACCTT[A/G]TAAATCAATTCTAAT | 9690 |
rs187000333 | snp | C/T | 0.013105 | 0.08 | intron-variant | UBE3C | GRCh38.p7 | 7:157247520 | AATATGGCAAAACCC[C/T]GTCTCTACTAAATAT | 9690 |
rs187022080 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157166672 | TTGAACTCGGGAGGC[A/G]GAGGTTGTGGTGAGC | 9690 |
rs187066634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166836 | ATTCCTTTGGAGATG[C/T]CGTATTTCCTTGTTT | 9690 |
rs187069850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178479 | TAGTGCCAGCATACC[A/G]TTTGGCACATAACGA | 9690 |
rs187081628 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157151134 | GTCGGGCTCCACCCC[A/C]TAAAGGGCAGCAGTA | 9690 |
rs187098608 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157190406 | TGCAGTGTCCTGCAT[A/G]GTAGCCACCAGTGAC | 9690 |
rs187100551 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157162755 | ACTCCTGTGCTCAAG[C/T]GATTCTCCTGCCTTG | 9690 |
rs187125896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157244185 | CAGTGAGCTGAGATC[A/G]TGCCATTCATTGCGC | 9690 |
rs187156740 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157223875 | CAGTGAGCCAAGATC[A/G/T]TGCCAGTACACTCCA | 9690 |
rs187205390 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264338 | TATTACAGGTGTGAG[C/T]CAACATGCTCGGCCT | 9690 |
rs187210665 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157214803 | TAAAATGAATGACTT[C/T]CAAGAATTAGTGTAT | 9690 |
rs187218339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178269 | ATTGTTCTATTTGGG[G/T]GATATTGCAGGCGTG | 9690 |
rs187232573 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217236 | GCCTTAATGATTCTT[C/T]GTGAGGTTGAAAAAT | 9690 |
rs187258026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157240503 | GAAGTGAGACCAGCC[A/G]TGTGGGTTACTTTTT | 9690 |
rs187299412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182053 | TGATTTTAATCAGTG[A/T]TTGGATGGACAGTAT | 9690 |
rs187306068 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | UBE3C | GRCh38.p7 | 7:157153996 | AGCGAGGCCCTGTCT[C/G]GGGGGGGAAAAGTTA | 9690 |
rs187306759 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157215281 | CCCAAGTACCCTTCC[C/T]CTTTTTTCTTGGGCA | 9690 |
rs187320906 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157196743 | GGAGTCTGAGGTGGG[G/T]GGATCACCTGAGGTC | 9690 |
rs187448584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234289 | TGTATGTTCTTCTGA[C/T]GGTGTTGTAGTTTTA | 9690 |
rs187466862 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157229647 | TAAATTTTTATTTTA[A/G]AGATGGGGGTCTCAC | 9690 |
rs187470923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199349 | ACGTTAACACTCTTA[C/T]CAGGCATATGGTAAG | 9690 |
rs187499035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157252517 | TTTAAAATGTGAAAC[A/G]TTAAAAGAAGCAGAT | 9690 |
rs187504778 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157169349 | ACAGTTGAAAATCAA[A/C]ATAGAAGGAAGTCAT | 9690 |
rs187514980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265993 | TAGATGTTCTACCTC[C/T]CTCAATTTCGTCTTG | 9690 |
rs187523720 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157246815 | TGTTCTCCACACCCC[C/G]GGGGGTAATTAGACT | 9690 |
rs187527729 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157218804 | GGGTTAGGAGCCTGT[A/C]TCTAGCTGGTCATGG | 9690 |
rs187534005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245922 | CTTGAACTCGGGAGG[C/T]GGAGGCTGCAGTGAG | 9690 |
rs187537634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219275 | TCAGCTGAACCCAGC[A/G]GTGTGCTTAGTGATT | 9690 |
rs187537773 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157254860 | GCCTGGGCAATGTGG[C/T]GAAATCCCATCTCTA | 9690 |
rs187545083 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269167 | GGGTTGGTCTTTTTT[A/G]TTTTAGGTTGTTTTA | 9690 |
rs187556834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184363 | CCTTTTTACCCTATC[C/T]TGTGAACACCGGGTA | 9690 |
rs187647408 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157185019 | CAAGTATTCATTTTT[C/T]TGTATGTTTATAAAA | 9690 |
rs187654881 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157202176 | AAACATTAGAACAGT[A/G]TAGAAGTTTTTAAAC | 9690 |
rs187688682 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157188311 | TCTTTGAAATGAACT[G/T]TAAGTAAGGAACCCA | 9690 |
rs187705380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160016 | AGGAATCAAGTTTCA[G/T]ATAGGACTTTTTATA | 9690 |
rs187713252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173323 | CAAGGCTGCAGTGAG[C/T]TATGATCCTGCGACT | 9690 |
rs187745201 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251833 | TAAAAGTAGTGTAAC[C/T]GTTTAAAAGTTATTA | 9690 |
rs187749543 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157179566 | AAGAACCTTTGGTCT[C/T]GACATCCTCATAGGT | 9690 |
rs187757812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157233334 | CTTTCTCTGCCACCT[A/G]GGCTGGAGTGCACTG | 9690 |
rs187769577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205012 | GGTCTCACTGATGGT[C/G]AGTAATTCACCTAGC | 9690 |
rs187770559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157230565 | CCAGGTGTGGTGGCA[C/T]ACGCCTGTAGTCTTA | 9690 |
rs187772691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157221479 | AGGCGTGGTGGCTCT[C/T]GCCTGTAATCCCCAG | 9690 |
rs187780148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151900 | TCACAGTAAAGTGGC[C/T]GTCATCTGAGAACTC | 9690 |
rs187785202 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157205787 | TGTAGCATGTGGACA[C/T]AGTGTATCTTCTCTG | 9690 |
rs187786528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200223 | GGAAATTTCACATGC[C/T]CTTTCATGCTTTTAC | 9690 |
rs187787113 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233781 | TCATACAGTACTCCA[C/T]GTCAAAGTGTCTGCA | 9690 |
rs187799559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201193 | GCCAGGCGTGGTGGC[A/G]GGCACCTGTAATCCC | 9690 |
rs187811170 | snp | C/T | 0.0014985 | 0.0273314 | intron-variant | UBE3C | GRCh38.p7 | 7:157170290 | TGGGTCATTTTGTTT[C/T]GTTTTTCTTCCAGTA | 9690 |
rs187832891 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138401 | CATGGTAAATATTTA[C/T]GTCCGTCTGTGCGTG | 9690 |
rs187852038 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254934 | CGTGGTGGCGTACAC[C/T]TGCAGTCCCGGCGTG | 9690 |
rs187853648 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157261188 | GTGCATGCCTGTAGT[C/T]CCAGCTACTTGGGAG | 9690 |
rs187872336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224991 | TTATAAATGAAAATA[C/T]TCTATCGCAAGGGGT | 9690 |
rs187943278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156151 | CATTATATTGAGCTG[C/T]TTTTAGAACTTGTTC | 9690 |
rs187949482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157192277 | CTAAATCCCTACCAC[A/G]TTTTTAAAGTTTTCT | 9690 |
rs187960014 | snp | C/T | 0.013195 | 0.0801462 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139234 | CCCGCCCGGCTGCTT[C/T]CGCGGCGGCGCTGCC | 9690 |
rs187964172 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175346 | AGCCAAAAGAGGACT[C/T]CTGATGTGTGAGAAT | 9690 |
rs188022205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157220872 | TTTTTCATAAACTTA[C/T]ACAGCCATGTCACTC | 9690 |
rs188043810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157188056 | TTTTCTCTCCCTCCA[A/G]TTTGAGTGATATGTT | 9690 |
rs188050132 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157167014 | AGCTCACTGCAACCT[C/G]CACCTCCTGGCTTCA | 9690 |
rs188053454 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172064 | GACGGAGTCTTGCTC[A/C]CTCTGTCGCCCAGGC | 9690 |
rs188059481 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157211952 | CAGCTGCTGCGTCAT[C/T]TGGCACTTGACTCAC | 9690 |
rs188076895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157565 | TTCAAATGCACATAG[C/T]CTTTGACCTACAAAG | 9690 |
rs188079166 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157194214 | TACAGGTTGTTTTCA[A/G]TTAAGTGAAAAGGAG | 9690 |
rs188080269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183344 | TTGGGATTGGTAATT[A/G]ACTAAGACAGTTCAC | 9690 |
rs188085275 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157141224 | TGGTTAAGGAATCTG[A/G]GTGGGGAGCCAGCTG | 9690 |
rs188093969 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157155430 | TCACAGTTTTTTGGG[G/T]TTTTTTTTAAATCAA | 9690 |
rs188117796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238033 | CTCCAGCCTGGGTGA[C/T]AGAGACCCTGTCTCA | 9690 |
rs188131801 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157238908 | ATAAAGACAGTGTTT[A/G]AAAGGAAGAGAAAGG | 9690 |
rs188141023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225100 | CTCTGCCTCCCGGGT[G/T]CACAAGATTCTCGTG | 9690 |
rs188143842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255576 | CTTTCCTTTGCCAAG[A/G]GATTGTCTTCGGTTG | 9690 |
rs188145571 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157186727 | ATTTTGAGATGATGC[A/C]TAGCTTTCTTTGCCC | 9690 |
rs188283823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157240769 | GGGAGTCAGTGTAGC[A/G]GTGGTTAGAGCTAAG | 9690 |
rs188299643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221751 | TCTAAAAAAAAAAAA[A/T]TTGGCCATTGTAAAA | 9690 |
rs188302350 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157229581 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 9690 |
rs188308661 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157217071 | AAAATTATTTATTTT[A/T]TGACTCATATGACTA | 9690 |
rs188310523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173974 | TTCATTGTTTAATAA[C/T]GTTTTATGGCAAAGA | 9690 |
rs188313686 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157189172 | GTCTGAATATGCCGA[A/G]GAAGCTGGGGCTGGA | 9690 |
rs188314090 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160665 | AATTTTCTGTCTTTC[C/T]CTTGTTAATTGATCT | 9690 |
rs188315527 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157143142 | AAAGTGCTGGGATTA[C/T]AGGTATGAGCCACTG | 9690 |
rs188320651 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143807 | CAGATTTGGGGGTTA[C/T]CAACAGAATGGTGGC | 9690 |
rs188322079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157161014 | ACAGCATCCAGGACA[C/T]GAAAGATGAAGATAA | 9690 |
rs188363501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157259779 | CGGATTGTGGGGGTC[A/G]CTGCGGAACTCTGTA | 9690 |
rs188371487 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | UBE3C | GRCh38.p7 | 7:157243576 | GGCCTGGCCCCTCCC[A/G]GGGAGCTTGGTGTCC | 9690 |
rs188377869 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157261523 | AGTGTTTTTGAAGTT[G/T]TTATATGTTAGACAT | 9690 |
rs188410695 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237832 | GGGAAGAACACTTAA[A/G/T]CCCAGGAGTTCAAGA | 9690 |
rs188481685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157146881 | GTCTTGAACTCCTGA[C/T]CTGAAGTGATCCGCC | 9690 |
rs188537918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195206 | AAAATTAGAGACGGG[A/C]TTTTCCAGGAAAGAT | 9690 |
rs188546117 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231370 | CCTCGGACCAAAAGA[C/T]GTTGACATTTTATGT | 9690 |
rs188546455 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157210126 | AGGTTGCAGTCAGCC[A/G]AGATAGCGCCACTGC | 9690 |
rs188549915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157177624 | CCTCGAGAGACACCA[A/G]TGTGGTGCTGAGGGG | 9690 |
rs188550717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175475 | AGCATAAGCCACTGC[C/T]GTGACTTTCTTGCAT | 9690 |
rs188580228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157206483 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGACCTTG | 9690 |
rs188582388 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157257688 | GTTGCAGTGAGCCGA[A/G]ATCGCGCCACTGCAC | 9690 |
rs188590503 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157173543 | TATGGCTATTTCTTC[C/T]TCACCTCCTTTTTAA | 9690 |
rs188598655 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157227606 | TCAGGAGGCTGAGGC[A/G]GGAGAATGGCATGAA | 9690 |
rs188612329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157142890 | TGGAGTTTCGCTCAC[A/G]CTGGAGCGCAGTGTT | 9690 |
rs188780164 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157267415 | CGACAGAGCTAGACT[C/G]CATCTCAAAGAAAAC | 9690 |
rs188799959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226233 | AAAATAAGTGCCATT[G/T]CAATCCAAGTTTCTT | 9690 |
rs188807811 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157246951 | ACTGGAGTGCAGTGG[C/G]ACAATCTCGGCTCAC | 9690 |
rs188814821 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157213178 | CACAAGAGTTAACAC[A/G]TCAGATGGACATAAT | 9690 |
rs188818156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157262311 | TGGATTTTAGCACAT[A/G]TTATATGCCACATAT | 9690 |
rs188821508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192714 | AAAATGAGCTGCCTT[C/T]GTCGAGAGTGCCCTT | 9690 |
rs188827442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224663 | GTTCCGTTCTTCAGT[A/G]ATGGCTTCAAGAGTG | 9690 |
rs188855723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163676 | CTCAGATTCTCTCAT[C/T]TGATTAAGTCAAGAC | 9690 |
rs188898009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150208 | CGTGGTGAAACCCCA[C/T]CTCTACTAAAAATAC | 9690 |
rs188906784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258930 | TCTTTTCATGCATTT[A/C]TTTCCTGAATCATTT | 9690 |
rs188910030 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265742 | GAACATTTTCTCATG[C/T]GTGCATTTCATCTCT | 9690 |
rs188927078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157241924 | GATCACCAAAGACAT[C/G]GTTCCATTTATATGA | 9690 |
rs188975720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180957 | AAAGCCCACCCCGGG[A/G]CCCCAGGTGGAGCAG | 9690 |
rs188984495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157198323 | GACTTGGAAGATTTG[C/T]GCTTCACTTCATCTT | 9690 |
rs188986993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167953 | AACATTTTAAAGATA[C/G]TCTCAAGTCAATGAA | 9690 |
rs189008399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153237 | TCAGTTTTGTACATA[C/T]TATTTTAGAGCTGTG | 9690 |
rs189025912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157264565 | TGAGCCAACATGCTC[A/G]GCCTGTTACACACAC | 9690 |
rs189065654 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157216734 | AGCCCTTTTCTGTGA[A/G]CGGGTTTGGTGTCCG | 9690 |
rs189069776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157228994 | GCTTCTAGAGGTTAC[A/G]TGTCCCTTGAGATGC | 9690 |
rs189098676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164727 | TATTGAGAACTTACT[A/G]TGTATGTACTAGGTA | 9690 |
rs189131771 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157145802 | TTACAGAATAATTGA[C/T]GGGAAACTATAATAG | 9690 |
rs189166926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157220071 | CAAAAATTAACCAGG[C/T]GTGATGGTATACACC | 9690 |
rs189180011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157235060 | GCTGGGCGTGGTGGT[A/G]CATGCCTTTAATCCC | 9690 |
rs189185035 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157207077 | ACATGTGTGTCTTGA[A/C]TAGTGGCCTTATTAG | 9690 |
rs189188172 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157266527 | TGGGATCGATCTCTG[C/T]GTCAGAATTCCTCTT | 9690 |
rs189201358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157181781 | AAATTCAGGTTTTTA[C/T]TTTATTAGTGTTGAT | 9690 |
rs189202461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157190353 | TTTGGTGAACAGGCC[C/T]GTCATCTACTTGGTT | 9690 |
rs189214629 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157174299 | ATATATGAGAAATAC[A/C/T]GTATTTCTCATATAT | 9690 |
rs189215198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157153920 | ACGGCTTGGTGGGGC[A/G]GGGGCGAGGTTGCAG | 9690 |
rs189221342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206617 | TCTTTGAAACAGAGT[C/G]TGGCTCTGTTCCCCA | 9690 |
rs189243156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171272 | GCTGGAATTACAGGC[A/G]TGTTACCAACATGCC | 9690 |
rs189253374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157140339 | TGCTGTGGGGCTGTG[C/T]TTGGTGGTTTCTGAG | 9690 |
rs189253404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156790 | CCCCTTAATAATACT[C/T]TCGGAGACAGTTCCT | 9690 |
rs189272562 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157152357 | GACTTAGGTTTTAGA[C/G]ATGCGTGGGGGGCAG | 9690 |
rs189373134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157176565 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCAAACCC | 9690 |
rs189373523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157140883 | TCTTTTTATTGAGGT[A/G]TAACTTAAGATACAG | 9690 |
rs189404828 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147569 | TGTTTTATTGTCTTA[C/T]TGCATTAGGTAGGAT | 9690 |
rs189420697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262834 | ATGTGGGTGTGGCCA[A/G]TTGGGTGCCTGTTGT | 9690 |
rs189429710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267185 | TCCCAGCACTTTGGG[A/C]GGCAGAGGTGGGCAG | 9690 |
rs189438368 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157202378 | GAAGTCTAAGCCGGC[C/T]GGGCGCGGTGGCTCA | 9690 |
rs189451355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202628 | TGCCACTGCAGTCCA[C/G]CCTGGGTGAGAGCAA | 9690 |
rs189451849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157235592 | CTTTGGAATATGTAT[A/G]TATTTACAGAAGATC | 9690 |
rs189458196 | snp | C/T | 0.000997359 | 0.0223088 | intron-variant | UBE3C | GRCh38.p7 | 7:157223206 | TTGTCAGTGGGAATG[C/T]AGGGGAAAGTACAAG | 9690 |
rs189467036 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157171787 | TCTCGGCTCACTGTA[A/G]CCTCCGCCTCACGGG | 9690 |
rs189469590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157253591 | CCTCCAGAATGAGTC[A/G]CTTTTTCTCTTCTGA | 9690 |
rs189472054 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157198678 | CAGCTGGGATTACAG[A/G]CATGCGCCACCACAC | 9690 |
rs189478798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157253293 | CCAGGTCTGTGTTTC[C/T]GCTGTGTTGCTTTTC | 9690 |
rs189499311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157221854 | CATGAATTTGTTTTT[C/T]TGTTGTGTTTTCTTG | 9690 |
rs189505407 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157168591 | TGGTCCATCCATACA[A/G]TGGAACATTACTCTT | 9690 |
rs189683142 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157256671 | GCACTGAATGTGTGC[C/T]AAGCAATATAGTGTC | 9690 |
rs189684628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240335 | GCTGGGATTATGGGT[A/G]TGAGCCATAGCACCC | 9690 |
rs189703822 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256386 | GACCTCAAGTGATCC[A/G]CCAGCCCGGGCCTCC | 9690 |
rs189721007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157219636 | GCTGGGCACGGAGGC[C/T]CACATCTGTAATCCC | 9690 |
rs189737912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157219 | GCTAGTGATGTGGAC[A/G]GTAATAGTCCATGCT | 9690 |
rs189765755 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157230351 | AGAGGAATAATTGTC[G/T]TGGGCCACAGACAAA | 9690 |
rs189782019 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157245440 | CTCGTCATTCATTTC[A/G]AAGTGATGCCGTTTA | 9690 |
rs189799317 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157188197 | CAGTAAGTAAGCAGG[G/T]CTGACGTTAATTCAC | 9690 |
rs189809584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205187 | AAGAGACCTGTGTCT[C/T]GTTTGTGCCCTGTCT | 9690 |
rs189811848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173162 | GAGGATCCCTTCAGG[A/C]CAGGAGTTTGAGACC | 9690 |
rs189818419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214609 | TTTATTTAAAGTATC[A/G]ATTTAATTGGTCACA | 9690 |
rs189818437 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157226381 | GAAAGTTCGTGTGCT[A/G]TTAACCTCTAATATA | 9690 |
rs189830583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157159080 | TGTGAAGTCATGGGC[A/G]GTAACTACCAGCACC | 9690 |
rs189850490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191182 | ATTATGTCTTGTGTT[A/G]TTAATCATTGTGATT | 9690 |
rs189879114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163039 | AGAAATTGATTTCTT[C/T]ATTGAAATTTTTATT | 9690 |
rs189881140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157145206 | GGATTGTGCCAGCGC[A/G]TTCCAGCCTGGGTGA | 9690 |
rs189935966 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208806 | ATGGAAAAAAAGAAA[A/G]GGAAAAGGGTGCTTG | 9690 |
rs189942648 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157223881 | GCCAAGATCGTGCCA[C/G]TACACTCCAGCCTGG | 9690 |
rs189976524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242459 | AAGATGTTTTCTTCT[A/G]ATTGTTGAAAATAGT | 9690 |
rs189986035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240215 | ACCCACCACCACGCC[C/T]GGCTAATTTTTGTGT | 9690 |
rs190007268 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157239424 | GAAGGCAGGATCCTG[A/T]TGCTCCTGGGAGGGT | 9690 |
rs190023692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157212483 | CGTAAGAATATTTCC[C/T]CAAGGTCAGTTAAGC | 9690 |
rs190027767 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157177118 | CTACCAAACTTAGGA[A/C]AGCAGCATAGGAGAG | 9690 |
rs190041080 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157260894 | TGTGCCTAGGAGTGC[A/G]AGAGCCTTCTCCACC | 9690 |
rs190112114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157165440 | TCTCACTTTGTCAAC[C/T]GGGCTGGACTGCAGT | 9690 |
rs190120480 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157148932 | TGGCTCTGAAAATGT[G/T]AATTGACTGTCAGGA | 9690 |
rs190141955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157148277 | GGCTAATTTTTTTGT[A/G]TTTTTAGTAGAGATG | 9690 |
rs190193667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259524 | CTGCTAGTAAATACT[A/G]TAGATTAAGAGATAT | 9690 |
rs190195309 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157167339 | AGCTTTGTAGATGGC[A/C]TTCATAGAAGACATG | 9690 |
rs190212408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235952 | ATCTTCAAGAGAAGA[A/G]AACTGTATATTGATT | 9690 |
rs190217041 | snp | A/G | 0.000181454 | 0.00952334 | intron-variant | UBE3C | GRCh38.p7 | 7:157248598 | GAGGGGTCAGGAGGA[A/G]GATTCACATACCTGT | 9690 |
rs190238377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228594 | AAATTTATTCCAGAA[G/T]CAGGAAAGCAAGCTG | 9690 |
rs190246743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225820 | TCTGGATGTGTTAGC[A/G]TGCCCCTGTTGTCCC | 9690 |
rs190257034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256119 | TTTATAGTTACAGGG[A/T]GATCCTTATTCTAGC | 9690 |
rs190264376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194674 | GAATACCTCGATTGC[A/G]GTAAAATATCTAAAT | 9690 |
rs190267553 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157197389 | AGCCAGTCCTTCAAC[A/T]AAAAACTCAAACATA | 9690 |
rs190275354 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157144288 | GCGACACAGCATGAC[A/C]CCATCTCTTAAAAAA | 9690 |
rs190290005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157265246 | TAGGTCTCTGAAACC[C/T]GTGCCAGATACTAAA | 9690 |
rs190335954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230020 | TTCAAGTGATTCTCC[G/T]GCCTCAGCCACCCAA | 9690 |
rs190349952 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157244380 | CAATTATTAAATAGC[A/G]TGTTGCTATTAGTAT | 9690 |
rs190395838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165204 | CATTATCTCTTCCAT[G/T]AGTGCTTTTGCTTCA | 9690 |
rs190457485 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157217752 | TAAGGCAGGAGAATC[A/C]CTTGAACCTGGGAGA | 9690 |
rs190461742 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157182917 | CCACACCCAGCTAAT[C/T]TTTGTATTTTTAGTA | 9690 |
rs190474899 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157200113 | GCCCCTTCATTTTCT[G/T]ATGCAAACATTGCTT | 9690 |
rs190485247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170062 | TGACCTCAGGTGATC[C/T]ACCTGCCTTGGCCCC | 9690 |
rs190495944 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157154744 | TGCATTGGATACTTC[A/C/G]TTTTTTCTCTAGTCA | 9690 |
rs190498947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157216236 | TAGTGCCGTTAGTAC[A/G]TTATTTCTCAGAAAA | 9690 |
rs190501761 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157202840 | AGCTCATTCGGTGGT[A/G]GGAAGACACATCTCA | 9690 |
rs190515160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162351 | TGGTATGTGCCACCA[C/T]GCCCGGCTAATTTTT | 9690 |
rs190516118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220217 | CCGTGTATCAAAAAA[C/T]AAAAAATTGTAAGGA | 9690 |
rs190516315 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157150293 | CAGAGGCGGGAGAAT[C/T]GCTTGAACCCAGGAG | 9690 |
rs190522167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166696 | GGTGAGCTGAGATCA[C/T]GCTGTTGCACTCCAG | 9690 |
rs190530141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157179930 | GAAAGTTGTGGAATT[C/T]GATCTTTTTAAAAAC | 9690 |
rs190537164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157172593 | CTGTAAACCGAGAAC[A/G]TGCAGAGAAGGAACT | 9690 |
rs190578535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232931 | ATTGAACCTTTTAAA[A/G]TGTACAGTTCAGTGG | 9690 |
rs190596708 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247611 | GCAGGAGAATCGCTT[A/G]AACCTGGGAGGCGGA | 9690 |
rs190625640 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157250735 | GATAATTTGGCGGGG[G/T]GGCTGTTACTGTCAT | 9690 |
rs190750915 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157169423 | CTCTGTTGCCCAGGC[C/T]AGAGTGCAGTGGCAT | 9690 |
rs190758960 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157154401 | TAACTTCCCACCATT[A/G]TTTTCTCAGTATCCT | 9690 |
rs190768024 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157195533 | ATGGTGCTGATGGCT[C/G]CTTTTTTCATCCCAA | 9690 |
rs190780296 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157166038 | AGGTGTCTAAATCTC[C/T]TGTGAGACAGGAAGT | 9690 |
rs190836663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265482 | GAGCAATCCCTAACA[C/T]GGTTTTTGCCTACAG | 9690 |
rs190842228 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218048 | AAAAAATATAAGTGA[A/T]GTTAACAGAGGGACA | 9690 |
rs190874963 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBE3C | GRCh38.p7 | 7:157236892 | ATCCACCACCATGCC[C/T]GGCTAATTTTTGTAT | 9690 |
rs190880750 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157233583 | CCACACCCAGTCACC[G/T]CATTTTGTTTACTTA | 9690 |
rs190939845 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157149137 | TCTCGGCTCACTGCA[A/G]CCTCCGCCTGCCAGG | 9690 |
rs191004353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177977 | GCTGTAAAATACCTT[A/G]TGAAAGCAACAGGAG | 9690 |
rs191046530 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157142322 | AGCTTTTTCTTTTTT[A/C]AAATTAAATACTTTT | 9690 |
rs191086863 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157254460 | TGGAGTGCAGTGGCG[C/T]GATCCCAGCTCACTG | 9690 |
rs191092445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157228406 | GTAACAAAGTTCCCT[C/T]GGGGCCTGGAGCTCA | 9690 |
rs191102754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258520 | TGCAGAGGGCAATGG[C/T]GTGATTTCCGCTCAC | 9690 |
rs191107260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224156 | TGGGATTACAGGCAT[C/T]AGCCACTACACCTGG | 9690 |
rs191107618 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157200855 | TCCTAGGCTGAAGCA[A/G]TCTGCCTCCTTTGGC | 9690 |
rs191111292 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157241559 | ATCAAACCAGGAACC[A/G]CAGGGTTGGTGAGGA | 9690 |
rs191147414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237740 | TATTTGTGCAATAAA[G/T]ACAACAAATAATCTA | 9690 |
rs191153361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157209359 | TATAATTTGGGCAGA[C/T]TGATGTAATATATGT | 9690 |
rs191157010 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243581 | GGCCCCTCCCAGGGA[A/G]CTTGGTGTCCTCCTG | 9690 |
rs191157593 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157224450 | CTGCCTGCCCCAGCC[C/T]CCCAAAGTGCTGAAA | 9690 |
rs191169548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192514 | CTTTGCTGGCAAGCA[A/G]CTGGAAGATGGATGT | 9690 |
rs191206877 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157254806 | AGCCTTTGGGAGGCC[A/G]GGGCAGGTGGATCAC | 9690 |
rs191225704 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268342 | TTTCCCCAAATGGGA[C/T]TAGCATGCTTGTTTT | 9690 |
rs191275652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158558 | TAGTCACAAAGCAAA[C/T]AAAATAATGGACAAG | 9690 |
rs191287458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233253 | ACTCATTTGAAGGGC[A/C]AAATCTTATTTCATT | 9690 |
rs191313642 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157204842 | TCAAAACAGTCTACA[A/G]TAGTATTCTGAAAAC | 9690 |
rs191325502 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157172845 | GTGCTGTGAGATGTC[A/G]ATTGGTGTCTCTCCA | 9690 |
rs191332706 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157211513 | TCCAGTTTTTAACCC[A/G]TTTGTGCCAGAGGTT | 9690 |
rs191342877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225045 | TTTGAGACAGAGATT[C/G]ACTCTGTCACCCAGG | 9690 |
rs191349424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157193801 | TTTGAGATGATTACA[A/G]ATTTAAGATGACTGC | 9690 |
rs191357536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157164597 | TGTGATAGTTTCTTT[A/G]AATAGCTTTATTTTG | 9690 |
rs191371718 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257880 | ATAATATATAATTAG[A/G]TAAGTACTGTATGTG | 9690 |
rs191379076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147373 | TTTCATGTACTAACC[G/T]TATGTCCTGAAATCT | 9690 |
rs191409659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142790 | ACCCCAAACCTCCGC[A/G]TCCTGCAGTATATTC | 9690 |
rs191493285 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157162812 | CATGAGCCACCTTGC[C/T]CAGCCTGGACCTTTA | 9690 |
rs191531752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220622 | GCACCAATTCTGTTC[A/G]AGTGTGATCAGGTCA | 9690 |
rs191572796 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157187492 | GCTCAAGCGATCCTT[C/T]CACCCCAACCTTCTG | 9690 |
rs191574457 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137407 | GGGGGACCACCTATA[C/T]ATAAACATGCCACCA | 9690 |
rs191576276 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157190651 | TATGTCATGGTTTGC[C/T]AGCCTGACTTGTGGA | 9690 |
rs191590396 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157178283 | GGGATATTGCAGGCG[C/T]GGAAAGTCTCAAAAG | 9690 |
rs191610927 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | UBE3C | GRCh38.p7 | 7:157157991 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 9690 |
rs191642579 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157240507 | TGAGACCAGCCGTGT[C/G]GGTTACTTTTTCTAC | 9690 |
rs191662963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215126 | AATACCCACCACTTA[C/T]AAAGGTGCATCTTTG | 9690 |
rs191670424 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157260598 | TGCCATTTGGTAATT[C/T]TGTCATTAACATTTA | 9690 |
rs191753144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144490 | TGGCATAACTTTCAG[A/T]GTCTTCGAGAATACC | 9690 |
rs191791583 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157215416 | ATCTCAACAATTGAT[G/T]GTGTGATCTTTATAA | 9690 |
rs191802902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157179164 | TGCAGTGCAGCTGCC[A/G]GTCCTTCACCTGACC | 9690 |
rs191812394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166837 | TTCCTTTGGAGATGT[C/T]GTATTTCCTTGTTTT | 9690 |
rs191816357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143315 | ATCTGATTTCAAGTA[A/C]AGAAATGGACTAAAA | 9690 |
rs191821912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207613 | CATCAGTTTTCATAG[A/T]CAGTAGAAAAGTTTT | 9690 |
rs191828191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174722 | CTCCCAAAGTTACAG[A/G]CGTGAACCACTGTGC | 9690 |
rs191835370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146262 | CTTTTTTTTTTTTGA[G/T]ACGAAGTCTCGCTCT | 9690 |
rs191836287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151416 | GGAGAAGATTGTATA[C/G]CTCTTTGGAAATGTA | 9690 |
rs191867928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227928 | CTTTATAAATGTTCT[C/T]AACTCAAATACTGTA | 9690 |
rs191925417 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141706 | CCACAAAGGTGACTG[C/T]CCTTCTGACCTCCAT | 9690 |
rs191927003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266194 | TGGCGGGAGCCTGTA[A/G]TCCAAGCTATGCGGG | 9690 |
rs191947595 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157257202 | GATGTATATATTTTG[A/G]TGCTAGTTTTATTTG | 9690 |
rs191957084 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157219441 | ACACCACCTAGGAAA[C/T]GTTCTCGCCAGAAAG | 9690 |
rs191966728 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157202330 | GTAAACTGACTTAGC[C/G]TAGTACTCTGTTGTT | 9690 |
rs191971474 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227165 | ATAGATGTGACAAAA[C/T]AATGAGTTTGCCAAT | 9690 |
rs191971825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196624 | TCTGGGAGGAACTGT[A/C]ATTACTTGATTTTAA | 9690 |
rs191975732 | snp | A/C | 0.00111841 | 0.023621 | intron-variant | UBE3C | GRCh38.p7 | 7:157231355 | TCATATAAAAATAGA[A/C]CTCGGACCAAAAGAT | 9690 |
rs191985774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157185184 | GAGGCTGTGGGCTTT[C/T]TCAGCGAGAGAGAGG | 9690 |
rs192005607 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157171423 | ATAAGCCACCATGCC[C/G]AGCCTTAGGGTCTCA | 9690 |
rs192035021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261575 | AATATTTAGGCTTTC[C/T]GGTTAGCTTAGTATG | 9690 |
rs192043654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246886 | ACATCTCTCTGAAGA[C/T]TGGATATTTTCTCTT | 9690 |
rs192063114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260005 | AGGTCAATCATCGAC[A/G]CCGTTATGTTCTGGA | 9690 |
rs192065221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146941 | CGGGAGTGAGACACC[A/G]CGCCCAACCATAGTA | 9690 |
rs192065748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175378 | ATTCCATTCCATAGG[A/G]GTCTCCACCAAAATG | 9690 |
rs192072493 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157229867 | GTCCTTCTGCCTTGG[C/G]TTCCCAAAGTGCTGG | 9690 |
rs192080849 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157199388 | ATATCTCAGAGATAG[C/G]GTATCTATTATCATT | 9690 |
rs192148848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182549 | TTATGAGGCCACACA[A/G]ATTATTTTAATAGAG | 9690 |
rs192163214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157196976 | CTCCATCTCAAAAAA[A/G]AGAATTGCTGAACTT | 9690 |
rs192207184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221545 | CAGGAGTTCAAGACC[A/C]GCCTGACCAACATAG | 9690 |
rs192219121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253344 | TTTATGGGAGCTCCA[C/T]GTTATACCTGCAAAT | 9690 |
rs192224171 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157167342 | TTTGTAGATGGCATT[C/T]ATAGAAGACATGAAA | 9690 |
rs192226927 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157206120 | TTGACTTGGTAGAGG[A/G]GACCATGGACTTTAT | 9690 |
rs192227296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233949 | CTGGTGACTAATAAT[C/G]TTGACCATCTTTTCA | 9690 |
rs192235612 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180892 | GAGAAAAGGCTGATT[A/G/T]TAGGGCGGGATGCAG | 9690 |
rs192237663 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157152595 | GAGCTCATTGATCTC[A/G]ACTTCTGATATGTGA | 9690 |
rs192276911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167140 | TTCACCATGTTGGCC[A/G]GGCTGGTCTGGGACT | 9690 |
rs192324021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155546 | ACTTTGACATTCACT[C/G]TAGTTTTTTAACATA | 9690 |
rs192406151 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157243838 | ATTCATGAATGCAGA[A/T]TTCCAGTATGTAATG | 9690 |
rs192415242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183375 | AGAACTCGGGAAGTC[A/G]AGGTGTGCGGGAATG | 9690 |
rs192428669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217431 | TGCTGGGATTACAGA[C/T]GTAAGCCACCACACC | 9690 |
rs192444008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163348 | GCCGAGATCACACCA[C/T]TGCACTCCAGCCTGG | 9690 |
rs192470268 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157252177 | CAGTTTTCTCTGATC[A/T]GGCAAGGTAATTGGG | 9690 |
rs192477854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157265828 | CTGTGATACAGGGAT[A/G]AGAATTTTCACACTG | 9690 |
rs192555833 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157216013 | AATATTGTAATTTTT[A/T]AAAACCATAATAAAA | 9690 |
rs192561959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179810 | CTACAGAAATTAAAC[A/G]CATACTCATTTCAGC | 9690 |
rs192606148 | snp | C/T | 0.000266126 | 0.0115322 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170354 | TACCTTGTCACAGTC[C/T]GGGGGCGCTTTTCCC | 9690 |
rs192611091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235148 | TGAGCCAAGGCCTTA[C/T]CATTGCACTCCAGCC | 9690 |
rs192612771 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184369 | TACCCTATCCTGTGA[A/G]CACCGGGTAGTGTCT | 9690 |
rs192621678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267037 | TGAGCTATGCGCCTG[A/G]CCTGGAATGTTATTT | 9690 |
rs192623911 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157156489 | TTTTTGTATTTTTCA[C/T]AGAGACAGGGTTTCA | 9690 |
rs192628521 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157139682 | TGGCTCCCTTCCATG[C/T]AGGAGGCCGGTGAAC | 9690 |
rs192648937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157238187 | AATTTTATTGTTTCT[A/G]AACTTAAAATCAGCT | 9690 |
rs192658560 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157225106 | CTCCCGGGTTCACAA[G/T]ATTCTCGTGCCTCAG | 9690 |
rs192663091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255773 | ATTATTTTAGGTTTA[G/T]GGAGCACTTTACTAG | 9690 |
rs192674714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239213 | ACAAAAATGTCCTTC[A/G]AAAGCATAATGATAA | 9690 |
rs192683224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151915 | CGTCATCTGAGAACT[C/G]TTCTGCACAGCCTCG | 9690 |
rs192685161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157212360 | CTTAATTTTTTGGTT[A/G]CAATACTATATCTAA | 9690 |
rs192717958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170187 | CAAGGACCGATAATG[A/G]TGTTTTCGTTGTCAA | 9690 |
rs192720015 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139015 | CGCTGGGCGCCCCTG[A/C]AGCGGCCCGAGCTGT | 9690 |
rs192784413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234695 | CCTGACTTCACTACC[A/G]TAACGGTATGTGTTA | 9690 |
rs192802510 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157206539 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCATA | 9690 |
rs192805774 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157254875 | CGAAATCCCATCTCT[A/C]CTAAAAATTAGCTGG | 9690 |
rs192822953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157193199 | TATTTTGAATCTTGC[A/G]TTATCTGATGCAAAT | 9690 |
rs192883063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140402 | AGAAGTGTGCTGATA[A/G]TTTTTCAGCTTTGAG | 9690 |
rs192887486 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157255171 | GGCAAAAAAAACCAG[A/G]TGTTTAACATAGAAG | 9690 |
rs192888800 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157163728 | GGATCTTTTTTTGGG[G/T]GAAAACATTCTGTAA | 9690 |
rs192948225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160168 | CAACTTCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 9690 |
rs192967136 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157189433 | AAAAATAAAGGCTCT[A/T]CTGCAGTATCAGACA | 9690 |
rs192974156 | snp | A/G/T | 0.0107304 | 0.0725162 | intron-variant | UBE3C | GRCh38.p7 | 7:157160910 | GATGCGTGTTTGTGC[A/G/T]TATAATCCTATGGAT | 9690 |
rs193009831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221813 | TTTGTGTCTACCAGC[C/T]GACTAATGATATTCA | 9690 |
rs193017333 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237859 | AAGACCATCCTAGGC[A/G]TACATAGGGAGACCT | 9690 |
rs193019319 | snp | C/T | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269560 | TGGCTCCCAGGCCGG[C/T]GGCCGGTGTGCTCCT | 9690 |
rs193034853 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210156 | CACTCCAGCCTGGGC[A/G]GTAGGGTGACTCTCT | 9690 |
rs193072041 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216266 | ACTCAGAAATACTCT[C/T]TCAGGAAAAAGTTGT | 9690 |
rs193072908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157241947 | TTATATGAAATGTCC[A/G]AAACAGGAAAATCTA | 9690 |
rs193085764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157175735 | ACCAAAGGTAGGAAT[A/G]AAGAACCTATTAGAA | 9690 |
rs193087771 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156792 | CCTTAATAATACTCT[C/T]GGAGACAGTTCCTGA | 9690 |
rs193126880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157201333 | TGTCTCAAAAAAAAT[A/G]AAAAGAAAAGTATAA | 9690 |
rs193140870 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157261218 | GGCTGAGGCAGGAGA[A/G]TGGCTTGAACCCGGA | 9690 |
rs193151031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176672 | AAATACAGTGTGTGA[C/T]AGATGACTTTTAATG | 9690 |
rs193157524 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157142971 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 9690 |
rs193161210 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157230874 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 9690 |
rs193169162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157198210 | TGCATATATTCAGAC[C/T]GCTTACAAAAGGAAT | 9690 |
rs193178159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157173325 | AGGCTGCAGTGAGCT[A/G]TGATCCTGCGACTGC | 9690 |
rs193231585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258987 | TCCCTAAATATCTCA[A/G]CACATACTTCCTAAG | 9690 |
rs193235022 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157228850 | CACATATCATAGACT[A/G]TTTACACTCCAGGTA | 9690 |
rs193298522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157218862 | AGCTAACTCTGAGTT[C/T]GCAAGGGTGCTAACA | 9690 |
rs193299943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246390 | CTCTGGAAGCTACTT[A/C]CTCCCATGTTATTAA | 9690 |
rs193302144 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157194266 | TTCCTCTAAATTATG[G/T]CACTGAGAAAACTTC | 9690 |
rs199504577 | snp | C/G | 0.000296619 | 0.0121746 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174982 | CAGTTGGATGGATCT[C/G]AGAGACTTACATGCT | 9690 |
rs199538407 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188772 | AAGTAGGCTTACTCT[A/G]ACTGTTACAGATTTT | 9690 |
rs199552078 | snp | A/G | 1.69951e-05 | 0.00291501 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182130 | GTTTTTACAGCCTTC[A/G]CAGAGGAGTTTCTGG | 9690 |
rs199566412 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193679 | TTTTTTTTTTTTTTG[A/C]TGAAAACATTCTTTA | 9690 |
rs199574006 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207541 | ATAACGAATTCTTCG[A/G]TGATCCCATAGAAGG | 9690 |
rs199609591 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157175668 | AATATTTGTTTAGGA[-/T]TACTGTCAGAACTAG | 9690 |
rs199626678 | snp | A/G | 2.97783e-05 | 0.00385853 | intron-variant | UBE3C | GRCh38.p7 | 7:157207973 | TGTTTACTGACATTG[A/G]AAAATGTACAAACTT | 9690 |
rs199635060 | in-del | -/TT | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157167540 | GCCTCTCTCTCTCTC[-/TT]TTCTTTTTTTTTTTG | 9690 |
rs199677174 | snp | C/T | 0.000453085 | 0.0150445 | intron-variant | UBE3C | GRCh38.p7 | 7:157254319 | TATTCAGGTATGTTA[C/T]CACTGCTAGTTATTG | 9690 |
rs199684379 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154318 | TTCGAGATTCTGTCT[-/A]AAAAAAAAAGATAAA | 9690 |
rs199719045 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254397 | TTATTTTAATTAATT[A/T]ATTTATTTTTTTTTT | 9690 |
rs199763738 | in-del | -/A | 0.239614 | 0.249784 | intron-variant | UBE3C | GRCh38.p7 | 7:157227542 | CTCTACTAAAAATAC[-/A]AAAAAAAAATAGCTG | 9690 |
rs199765177 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171686 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 9690 |
rs199807302 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157146662 | TATATTAAACTAAAC[-/T]TTTTTTTTAATTTGA | 9690 |
rs199836750 | snp | C/T | 0.00873301 | 0.0654999 | intron-variant | UBE3C | GRCh38.p7 | 7:157178682 | GAATACTTTTTTCAT[C/T]TTTACAGGTTGCTGC | 9690 |
rs199863249 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242525 | GTTGTTTTTTTTTTT[-/G]TTTTTTTTTTTTAAA | 9690 |
rs199863451 | in-del | -/TTCAC | 0.011124 | 0.0737446 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269272 | AAGAGAAATTGACAA[-/TTCAC]TTATTTGTGGTTTTT | 9690 |
rs199903783 | snp | A/G/T | 0.0176869 | 0.0926638 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139247 | TTCCGCGGCGGCGCT[A/G/T]CCCGCACATGGGCTA | 9690 |
rs199962159 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157973 | CAACAGATATATATA[G/T]ATATATATATATATA | 9690 |
rs199962406 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237897 | ACCACTAAAAAAAAA[A/G]AAAAAGTAGCCAGGC | 9690 |
rs199968140 | in-del | -/ACAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264407 | CATGCTCGGCCTGTT[-/ACAC]ACACACACACACACC | 9690 |
rs200032798 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192733 | GAGAGTGCCCTTCTG[A/G]TGAATGTGGTGCTGG | 9690 |
rs200049102 | snp | A/C/G | 0.000102088 | 0.00714387 | intron-variant | UBE3C | GRCh38.p7 | 7:157220805 | GACACAGGGTTACTG[A/C/G]GGTATGAATTACATG | 9690 |
rs200072169 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262684 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 9690 |
rs200090736 | in-del | -/ATATATA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171680 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 9690 |
rs200097530 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261147 | GCCTCTACTAAATAC[-/A]AAAAAAAAATCAGCC | 9690 |
rs200137968 | snp | C/T | 0.000181212 | 0.00951698 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248559 | CTTCACTGTGGTGAA[C/T]AATGACCTGGGAGAG | 9690 |
rs200141672 | in-del | -/A | 0.0387552 | 0.1337 | intron-variant | UBE3C | GRCh38.p7 | 7:157266186 | GGGCGTGGTGGCGGG[-/A]GCCTGTAGTCCAAGC | 9690 |
rs200199223 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256955 | ATTAAGGTCTTCTGG[A/G]GAGTTGTGGAAGGGT | 9690 |
rs200201917 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158434 | GCACAGAGTGGCAGG[C/T]CCGGTGTAGAGAACA | 9690 |
rs200237051 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157184846 | CAGCTCAGGGCTTGA[-/T]TTTTTTTTAAAAAAT | 9690 |
rs200298482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186791 | GTAGAGGACGTTCCA[A/G]TTGAGCACATTTATG | 9690 |
rs200313268 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142368 | TATAGATCTGTGTAC[C/T]ACAAGTCTGACTTGA | 9690 |
rs200426414 | snp | C/G | 1.75477e-05 | 0.00296202 | intron-variant | UBE3C | GRCh38.p7 | 7:157178657 | ACATTTTGCCATCCT[C/G]TAAGTGTGTGAATAC | 9690 |
rs200469612 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant | UBE3C | GRCh38.p7 | 7:157257056 | TAAGGTACACAACTT[C/T]CATGACATTTGCTTT | 9690 |
rs200471489 | in-del | -/AA | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157189387 | TTTTAAAATATGATT[-/AA]ATATTCACTGGCTAT | 9690 |
rs200492709 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159584 | GATTAAATACCATTT[A/G]CAGCTGGGTGCGATG | 9690 |
rs200497539 | snp | C/T | 0.000888449 | 0.0210579 | intron-variant | UBE3C | GRCh38.p7 | 7:157231043 | ATTGCTTGCTTGTAA[C/T]ATCTTTCCTCCTCAC | 9690 |
rs200520339 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201639 | CTTCAGTGTATCGCT[C/T]TTTTTTTTTTTTTTT | 9690 |
rs200545985 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157246739 | CTGCACCTCCAGACA[A/G]TAGGAAGGCCCGTGA | 9690 |
rs200579697 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194998 | GTGGCCTATTCAAGG[A/C]AAAAGCCACTAAAAC | 9690 |
rs200589933 | snp | C/G | 6.6569e-05 | 0.00576889 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170353 | CTACCTTGTCACAGT[C/G]CGGGGGCGCTTTTCC | 9690 |
rs200623608 | snp | G/T | 9.10871e-05 | 0.00674798 | intron-variant | UBE3C | GRCh38.p7 | 7:157182089 | GATTTTATAAAAAGC[G/T]TCTGTTTTTCTTTTT | 9690 |
rs200639306 | snp | A/C | 0.000610063 | 0.0174545 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254060 | ACAGGCAGATCCGCC[A/C]GCACTGCCTGGCTTT | 9690 |
rs200644525 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149058 | ATAAGGTTAAGAATT[-/C]CTTTTTTTGTTTTTT | 9690 |
rs200651408 | in-del | -/TG | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157180334 | TTTTAAAAAAGTCTC[-/TG]TGTATTTTTTAAAAT | 9690 |
rs200665790 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267590 | TGTTTTTCAGGAGTT[A/G]TATCCCGCATTTTGT | 9690 |
rs200683755 | in-del | -/AGGG | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157143975 | CAGGGAGTGAATCTC[-/AGGG]AGGGAGGAGTGACAG | 9690 |
rs200731607 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261298 | GCAACAAGAGCAAAA[A/C]TCTGTCTGAAAAAAA | 9690 |
rs200761950 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263752 | TTTTTTTATATTGGA[-/T]TTTTTTTTTTTTTTT | 9690 |
rs200778252 | snp | C/T | 0.00422596 | 0.0457725 | intron-variant | UBE3C | GRCh38.p7 | 7:157188999 | ACATGGAAAGATTTC[C/T]GAGACAGATGCGTAC | 9690 |
rs200822950 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237888 | CTGGTCTCTACCACT[-/A]AAAAAAAAAAAAAAG | 9690 |
rs200828555 | snp | A/G | 0.00049128 | 0.0156652 | intron-variant | UBE3C | GRCh38.p7 | 7:157207972 | TTGTTTACTGACATT[A/G]AAAAATGTACAAACT | 9690 |
rs200842012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217003 | TTTTTAATATTTATC[A/G]TTAAAAAATACATTC | 9690 |
rs200844106 | in-del | -/GGACTCGGGGTT | 0.477853 | 0.102875 | intron-variant | UBE3C | GRCh38.p7 | 7:157139400 | CGGGGCTCGGGGCTG[-/GGACTCGGGGTT]GGACTCGGGGCTGGA | 9690 |
rs200851892 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190552 | GATTAGAACACACCC[-/A]CCCTCACGGAAGGTG | 9690 |
rs200881738 | in-del | -/G | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157188807 | CTTTCAATTTTGATT[-/G]TTTTTAAAAAAGTAT | 9690 |
rs200885655 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157975 | ACAGATATATATAGA[G/T]ATATATATATATAGA | 9690 |
rs200889888 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193291 | AAAGAAAAATTTCAG[A/C]AGAACAAATTATTGC | 9690 |
rs200947822 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206574 | GCCTTTTTTCTTTTC[-/T]TTTTTTTTTTCCTTA | 9690 |
rs200949444 | snp | A/G | 3.31983e-05 | 0.00407407 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225522 | AAGATGCTTATGACA[A/G]ACTTTCTCCAGAAAA | 9690 |
rs200970689 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231917 | ATTACCACACTCTTT[G/T]GGGGGGGAGGGAGGC | 9690 |
rs200972407 | snp | A/G | 0.000148538 | 0.00861667 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220743 | AGGTTCCGGCGGATG[A/G]GGAGGATAGGCCCGC | 9690 |
rs200996558 | in-del | -/TC | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157244061 | CGTGGGGAAACCCTG[-/TC]TCTACTAAAAATACA | 9690 |
rs201008953 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261305 | AGCAAAACTCTGTCT[-/G]GAAAAAAAAAAAAAA | 9690 |
rs201036596 | snp | A/G | 0.000265243 | 0.0115131 | intron-variant | UBE3C | GRCh38.p7 | 7:157184062 | CATCTGGGGGGCTGC[A/G]ATGCAGGCAGCCCCG | 9690 |
rs201037074 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181578 | CAAGTATTGAATATT[C/T]TGATTTATCTCGAGT | 9690 |
rs201050873 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137672 | TGGGTTCAAGCAATT[C/T]TCCTGCCTTAGCCTC | 9690 |
rs201178438 | snp | A/G | 0.000716882 | 0.018919 | intron-variant | UBE3C | GRCh38.p7 | 7:157182364 | TTTACCTGAACACAC[A/G]TATGGGTAGCATTGG | 9690 |
rs201188504 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189756 | TGGGTTCTTTTTTCT[-/C]CCTCTTTCTCACTCT | 9690 |
rs201267897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157168178 | AACATGGTGAAACCC[C/T]GTCTCTACTAAATAT | 9690 |
rs201327047 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148731 | AAGATCAAATTAGTT[C/T]TTTTTTTTTTTTTTT | 9690 |
rs201353044 | snp | C/T | 1.67016e-05 | 0.00288973 | intron-variant | UBE3C | GRCh38.p7 | 7:157175046 | GCAGGTAAAATTCTA[C/T]TGTAAGTCAGTAACG | 9690 |
rs201353837 | in-del | -/AATTTTG | 0.0463947 | 0.145069 | intron-variant | UBE3C | GRCh38.p7 | 7:157234185 | AGAACGAACATTTTT[-/AATTTTG]AAGTCTAACGTGTTT | 9690 |
rs201354218 | snp | C/G | 0.00169293 | 0.0290448 | intron-variant | UBE3C | GRCh38.p7 | 7:157188949 | AACACTGATTGTCAG[C/G]GTGTACAAATGAATG | 9690 |
rs201356346 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162542 | TTTTTTTTTTTTTTT[-/T]GAGACAGGATCTTGC | 9690 |
rs201359092 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254393 | TATTTTATTTTAATT[A/T]ATTTATTTATTTTTT | 9690 |
rs201379638 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156941 | TCCTTATTATATGTG[A/G]AGACAGCCTTATTTA | 9690 |
rs201380877 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167152 | GCCAGGCTGGTCTGG[A/G]ACTCCTGACCTCAAG | 9690 |
rs201384626 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261299 | CAACAAGAGCAAAAC[A/T]CTGTCTGAAAAAAAA | 9690 |
rs201385096 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229930 | AATTTATTTATTTTT[A/T]TTTTTTTTGAGACTG | 9690 |
rs201415652 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234126 | GATTTGCAAGTATTT[C/T]CTTCTCTGGATTGTC | 9690 |
rs201457851 | in-del | -/AG | 0.485324 | 0.0843964 | intron-variant | UBE3C | GRCh38.p7 | 7:157237895 | TACCACTAAAAAAAA[-/AG]AAAAAAAGTAGCCAG | 9690 |
rs201467396 | in-del | -/TT | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157189392 | AAATATGATTAAATA[-/TT]CACTGGCTATATTTT | 9690 |
rs201477682 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204398 | AGGGAAACTTTGTTT[A/C]AAAAAAAAAAAAAAA | 9690 |
rs201484937 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185176 | GTGAAGATGAGGCTG[G/T]GGGCTTTCTCAGCGA | 9690 |
rs201533875 | snp | G/T | 0.000279213 | 0.0118122 | intron-variant | UBE3C | GRCh38.p7 | 7:157253944 | AGATCCTTACGTTTT[G/T]TATTCCCAGGTAGTT | 9690 |
rs201554425 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160080 | GTTACTTTTTTTTTT[C/T]TTTTTTTTTTCTGAG | 9690 |
rs201615154 | snp | A/G | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231266 | CCAACCCGGCTGCTC[A/G]GATGCTTGTGGGAGA | 9690 |
rs201619058 | in-del | -/TCA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193286 | TTAAAAAGAAAAATT[-/TCA]TCAGAAGAACAAATT | 9690 |
rs201627906 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215155 | TGATCTTGAGTGGGT[C/T]TTTACTATGCAGTTT | 9690 |
rs201636089 | snp | C/T | 0.00199806 | 0.0315443 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225465 | GAGATGGTCCATTTC[C/T]GGATGGAATTAATGT | 9690 |
rs201640404 | in-del | -/AAAT | 0.0799831 | 0.183287 | intron-variant | UBE3C | GRCh38.p7 | 7:157266318 | GACTCCGTCTCAAAA[-/AAAT]AAATAAATAAAAATA | 9690 |
rs201657659 | snp | A/G | 0.00024716 | 0.0111139 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182296 | CACCCTGGCTTTTCT[A/G]TTTCGTTTTAACTGT | 9690 |
rs201679814 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157149111 | CCCAGGCTGGAGTGC[-/A]AATGGCTCAATCTCG | 9690 |
rs201681513 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223262 | GTTTTAGTGGGTTTG[C/G]AGTCCCCGCCGCTGT | 9690 |
rs201686667 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268419 | GGATGTGAGGTGGGG[C/T]CTTCATTCATTGTCC | 9690 |
rs201729244 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157177944 | GTTTTTTTTTTTTTT[A/T]AAGAAAAAGGAAAAA | 9690 |
rs201735406 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200515 | ACACAATTGTGGCTA[A/G]AATGTTTATCCTGTC | 9690 |
rs201739709 | in-del | -/ATA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171684 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 9690 |
rs201745317 | snp | A/G | 0.00299542 | 0.0385842 | intron-variant | UBE3C | GRCh38.p7 | 7:157263888 | TCCTTCCTTTAATTA[A/G]TATGTGTTTTATCTA | 9690 |
rs201782129 | in-del | -/TA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171661 | CATTTTTAAATATTT[-/TA]TATATATATATATAT | 9690 |
rs201813782 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248193 | CATTGAATGCCTGCA[C/T]GGGATCCTGGAGCAC | 9690 |
rs201869768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157154314 | ACAGTTCGAGATTCT[A/G]TCTAAAAAAAAAAGA | 9690 |
rs201879222 | snp | G/T | 0.115788 | 0.21092 | intron-variant | UBE3C | GRCh38.p7 | 7:157157985 | ATAGATATATATATA[G/T]ATAGAGAGAGAGAGA | 9690 |
rs201881680 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260719 | TAAAAGGAAGTTTGG[-/A]AGGACCTGCTCCCAT | 9690 |
rs201893868 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206796 | CTTGATGGGTGAAAG[C/T]CTGCTGAGTAAAGAC | 9690 |
rs201913806 | in-del | -/CT | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157183424 | TCCAGGCACTCCACA[-/CT]CTCGGCACCTCCCTG | 9690 |
rs201918557 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207979 | CTGACATTGAAAAAT[C/G]TACAAACTTTTGTCT | 9690 |
rs201956089 | snp | C/T | 0.00199794 | 0.0315433 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183902 | CTGAGGAAGGGCTGC[C/T]GGTGTATTTGCGGGT | 9690 |
rs201961173 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229321 | TTTGGATTTTTGTTT[C/G]TTTGTTTTTTGAAAT | 9690 |
rs201970422 | in-del | -/AT | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157191796 | TATGTGTAGAATTAA[-/AT]ATATATATACCGTCC | 9690 |
rs202006020 | snp | C/T | 6.59e-05 | 0.00573983 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231103 | TTGAAAAAGCGGATC[C/T]GTGTGCACTTGCTCA | 9690 |
rs202051494 | in-del | -/ACATACAT | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157182677 | GTAGTATGTTTGAAA[-/ACATACAT]ACATACATACATGCA | 9690 |
rs202062799 | in-del | -/TC | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157236414 | GATTATTTGATATGA[-/TC]TTGGTTATATATTTG | 9690 |
rs202068244 | in-del | -/GA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158006 | AGAGAGAGAGAGAGA[-/GA]TACATATAAACATGG | 9690 |
rs202074370 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233015 | CAATGTCATCATCCC[-/A]AAAAGGAAACGCTAG | 9690 |
rs202090604 | in-del | -/CTT | 0.0275645 | 0.114116 | cds-indel, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267867 | GGCTCTCCTAAGCTC[-/CTT]CTTTCATTCTGCCAT | 9690 |
rs202131998 | snp | C/T | 3.3018e-05 | 0.00406299 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186892 | TGAAGAAGCTGGACA[C/T]AAAGCAGCAGACCAA | 9690 |
rs202189153 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157236393 | GATGGCATGCCTATA[-/T]AATCAGATTATTTGA | 9690 |
rs202202292 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169389 | TTTTTTTTTTTTTTT[A/T]AATTGAGACTGAGTC | 9690 |
rs202243973 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184039 | AGCCCGGTAAGCCCC[A/G]TGCCCTGCATCTGGG | 9690 |
rs367584671 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218755 | ATGCTGGAGAGCGAG[A/G]AAGCTATTGCAGGGT | 9690 |
rs367590985 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238192 | TATTGTTTCTAAACT[G/T]AAAATCAGCTTTGAG | 9690 |
rs367594881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265689 | GGAATACTGTGTCCA[A/G]TGTGCTCACCGTCTC | 9690 |
rs367598855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248220 | GCACAGTACCTGCCC[A/G]CTGAATATCAGCTTC | 9690 |
rs367731338 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157202350 | ACTCTGTTGTTGAAT[C/T]TTTCCTCTGCCAGAA | 9690 |
rs367764291 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163388 | GAGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs367795882 | snp | A/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207534 | ATACATGATAACGAA[A/T]TCTTCGGTGATCCCA | 9690 |
rs367806659 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226180 | TTTGTATAAATATTT[A/G/T]TATGAAATCACAAAT | 9690 |
rs367809463 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170783 | TAGGTCAGTGGGACG[C/T]GCACCCTGAATACCA | 9690 |
rs367827239 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159336 | GATTAAAAAAAAAAA[-/A]CAGAATTAGGATTAA | 9690 |
rs367835977 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189594 | TGTAGATGAGGCCTG[C/T]GGTGCCCACTCAGCC | 9690 |
rs367856558 | snp | C/T | 0.000217273 | 0.0104206 | intron-variant | UBE3C | GRCh38.p7 | 7:157231358 | TATAAAAATAGACCT[C/T]GGACCAAAAGATGTT | 9690 |
rs367900747 | snp | A/C | 8.43889e-05 | 0.00649518 | intron-variant | UBE3C | GRCh38.p7 | 7:157225552 | ATGGTATATATAATT[A/C]TTTCTGTGTATTATT | 9690 |
rs367930379 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237729 | TCTTTGGCTCTTATT[C/T]GTGCAATAAAGACAA | 9690 |
rs367930481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206294 | TGGAAACGGAGTCTC[A/G]CCCTGTTGCCCAGGC | 9690 |
rs367947975 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258515 | TGGAGTGCAGAGGGC[A/T]ATGGCGTGATTTCCG | 9690 |
rs367961907 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163826 | AGGAAAAGGCTTCTC[C/T]TTTACATCGTACTCA | 9690 |
rs367966559 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159429 | CCTACCCTGTTTTAT[A/T]AATATGTGAATATTA | 9690 |
rs367976010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198537 | CTGTATTTGTCTTTT[C/T]TTTTTTATTTTTTTC | 9690 |
rs367980419 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192033 | AACATTTCAGCACAT[A/G]GTGATCTTAAAATTA | 9690 |
rs367983378 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181986 | TATTAAAATGGTTAA[C/T]TTGGCTAATTTAGAA | 9690 |
rs368018606 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247066 | AGCTAATTTTTTTTT[-/T]ATTTAGTAGAGACGG | 9690 |
rs368020420 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248930 | TGCTTAGTCCTCACT[C/T]CTTGCCCGCTCAGAG | 9690 |
rs368023996 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196169 | GCAAGCCAAGGAATG[C/T]GGATGTTCTCTAGAA | 9690 |
rs368048935 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229067 | AGAGGGCAGCAGCGC[A/G]TGGGGCCTGTGAAAG | 9690 |
rs368067593 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209854 | TGCCTCAAAATGACT[A/C]CCTGCCACTTTATTC | 9690 |
rs368068418 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157154586 | ATAGTTTGATACTTA[A/G]TATAACCACTTTCCT | 9690 |
rs368068731 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138538 | GGGTGCCGGCCCCTG[C/T]ACCCCACCCTGCACC | 9690 |
rs368109453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147741 | CTAGTTTGCAGAATT[G/T]TATCATGAATGAAGG | 9690 |
rs368130387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146398 | CACCACACCTGGCTA[A/C]TCTAGTACAGACGGG | 9690 |
rs368142854 | snp | G/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138249 | GTTTATCAGGACAAA[G/T]CCCCATGGTAAGTCC | 9690 |
rs368176678 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244198 | TCGTGCCATTCATTG[C/T]GCTCCAGCCTGGGCG | 9690 |
rs368193068 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158051 | TACACTCTTTTTTCC[-/TT]TTTTTTTTTTTTTTT | 9690 |
rs368200737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261660 | TTCAGTTGAAGTACT[A/G]TAAATAGCAAAGGCA | 9690 |
rs368247491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157253294 | CAGGTCTGTGTTTCC[A/G]CTGTGTTGCTTTTCT | 9690 |
rs368271673 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179815 | GAAATTAAACGCATA[C/T]TCATTTCAGCCTTGC | 9690 |
rs368308795 | in-del | A/TTAAAAACCAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180582 | TTTAATGTGCTACCA[A/TTAAAAACCAT]ATACGCTTGTATATG | 9690 |
rs368356487 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241517 | CATAGCCACAGGCTG[C/T]CGCGCACACCCGCGA | 9690 |
rs368382891 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173511 | TTTCAAAGTTATTCT[A/G]TGCAAAAATCAACAT | 9690 |
rs368437032 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182781 | GGTATATAGAGTCTC[A/G]CTCTGTCACTAGGCT | 9690 |
rs368439356 | multinucleotide-polymorphism | ATTTA/TTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229928 | TTAATTTATTTATTT[ATTTA/TTTTT]TTTTTTGAGACTGTC | 9690 |
rs368486831 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198847 | AATTTATTTTTAAAA[-/G]TTTAATAGTTTGTTT | 9690 |
rs368531611 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162208 | TTAATTTTTTTTTCT[G/T]TTTTGAGACGGAGTC | 9690 |
rs368554407 | snp | G/T | 8.24083e-05 | 0.00641852 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178805 | GATGCTAGCTATGTG[G/T]TGTCAGTGATTGAAC | 9690 |
rs368554632 | snp | A/G/T | 0.000366384 | 0.0135301 | intron-variant | UBE3C | GRCh38.p7 | 7:157216835 | TGCTGCCGAGCTCAC[A/G/T]TGTGTGACGCGGATA | 9690 |
rs368557410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184346 | TGTTGGGTCAAAAAG[A/G]TCCTTTTTACCCTAT | 9690 |
rs368562816 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258238 | AGGTGTGAGCCACCA[C/T]ACCATGCCCAGCTGG | 9690 |
rs368587897 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158801 | TAGAAGAAATGCTTT[A/G]AAATCTATTGTTGAT | 9690 |
rs368588004 | snp | A/G | 0.000117266 | 0.00765633 | intron-variant | UBE3C | GRCh38.p7 | 7:157207951 | GTATAGAGTATATGT[A/G]TTTTTTTGTTTACTG | 9690 |
rs368590948 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252637 | TGACTTAAGTCAGGC[G/T]CTCTAGCACATTTGT | 9690 |
rs368626341 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243183 | GGTCCCCATCCCCCA[A/T]CCTCTGTGCCCTGCA | 9690 |
rs368641441 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199713 | TGACCTCAAGTGATC[C/T]ACCCGCCTCAGCCTC | 9690 |
rs368649985 | snp | C/T | 1.66529e-05 | 0.00288551 | intron-variant | UBE3C | GRCh38.p7 | 7:157186784 | TTGTAGTGTAGAGGA[C/T]GTTCCAGTTGAGCAC | 9690 |
rs368668513 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236128 | TTAAAAGTTCCATTA[A/G]CAAATGATTCTTGCT | 9690 |
rs368670932 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205526 | GTCATAGGCAGGGCT[A/G]TTGAAAGAAGCCACC | 9690 |
rs368685592 | snp | A/G | 1.66454e-05 | 0.00288486 | intron-variant | UBE3C | GRCh38.p7 | 7:157231342 | GGTAAAGTAACCTTC[A/G]TATAAAAATAGACCT | 9690 |
rs368702580 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261162 | AAAAAAAAAATCAGC[C/T]GGGCATGGTGGTGCA | 9690 |
rs368739239 | snp | A/G | 3.33372e-05 | 0.00408258 | intron-variant | UBE3C | GRCh38.p7 | 7:157254181 | GGACACGCTTGTCAC[A/G]GGAAATGAACAGGCT | 9690 |
rs368750113 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199380 | GATTTTAAATATCTC[-/AG]AGATAGGGTATCTAT | 9690 |
rs368778915 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266268 | GCAGTAAGCCGAGAT[C/T]GCACCACTGCACTCC | 9690 |
rs368825853 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186553 | GATGTAAAAAAAAAA[A/G]GTAGGAAATGAAGTT | 9690 |
rs368830188 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141148 | CATTCTTCTGGGAGA[A/G]AGTGGCAGTAAAGAG | 9690 |
rs368837864 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196883 | CTGAGGCAGGAGAAT[A/C]TCTTGAACCTGGGAG | 9690 |
rs368848092 | in-del | -/TTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236405 | TATAAATCAGATTAT[-/TTG]ATATGATCTTGGTTA | 9690 |
rs368848926 | snp | C/T | 0.000414027 | 0.014382 | intron-variant | UBE3C | GRCh38.p7 | 7:157169134 | GCAAGTAAGTTTGTT[C/T]TAAAATGAGGAGATT | 9690 |
rs368850380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227420 | AACTACTCCCTGGGC[A/G]TGGCGCAGTGGCTCA | 9690 |
rs368856320 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220493 | AAAACATAGTTAACT[A/G]TAAAAGTATGAAAGG | 9690 |
rs368858162 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222192 | CATGTTTTTTAGTTA[C/T]TGAATTTTGAGAGTT | 9690 |
rs368862781 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172108 | TGCGATCTCAGCTCA[C/G]CGCAACCTCGCCTCC | 9690 |
rs368881805 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156731 | AAAAAAAAAAAAAAA[A/C]ACAAGCTAGAGCATA | 9690 |
rs368922495 | in-del | -/TAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189386 | ATTTTAAAATATGAT[-/TAAA]TATTCACTGGCTATA | 9690 |
rs368951310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198684 | GGATTACAGGCATGC[A/G]CCACCACACCTAGCA | 9690 |
rs368970361 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230288 | GCTTTTAAAAGATCA[C/T]GTAGATCAGGGTTGT | 9690 |
rs369004583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260540 | AGAGCAGGAGGACTG[C/T]AGGTGAGGCGTGCAG | 9690 |
rs369008199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229235 | TTCACTTACTTCCCC[A/G]AAGCTGTTCTCTGAT | 9690 |
rs369014308 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250593 | CTCCCAAAGTGCTGG[G/T]ATTACAGATGCAAGC | 9690 |
rs369021999 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224161 | TTACAGGCATCAGCC[-/AC]TACACCTGGCCTGGA | 9690 |
rs369062719 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255043 | ACTGGAGGTGGGAGA[C/T]GGAGGTCGTGAGATC | 9690 |
rs369070971 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | UBE3C | GRCh38.p7 | 7:157183857 | TAACTAAAATACGTT[C/T]TAACTGATTGTTTTG | 9690 |
rs369155279 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194185 | TTTGAAATGGGGCTG[A/G]CTGTTATACATTATA | 9690 |
rs369161781 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157153177 | CACTTCAGCCTGGAT[C/G]AAAGAGTGGGACTCC | 9690 |
rs369184870 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231497 | TGGTTGTAAGTAGGT[G/T]CTATGGTTTGAATGT | 9690 |
rs369225734 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200352 | TACTTCATGATTCCT[A/G]TGGTGTACTCAGAAA | 9690 |
rs369233574 | snp | C/T | 0.000247821 | 0.0111288 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181668 | CCTGTCCGGAAGGTG[C/T]GAGGTGAGACTGGAA | 9690 |
rs369235276 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203064 | GTAGAGCAAAAGATA[C/T]TCATATGTTGTTCAG | 9690 |
rs369242523 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255270 | AAATGCCACTTACAT[C/T]CAAATGAGATAACCC | 9690 |
rs369247139 | snp | A/C/T | 1.80104e-05 | 0.00300081 | intron-variant | UBE3C | GRCh38.p7 | 7:157170271 | TGTCCAAATACTATA[A/C/T]TTATGGGTCATTTTG | 9690 |
rs369248519 | snp | A/G | 1.68872e-05 | 0.00290574 | intron-variant | UBE3C | GRCh38.p7 | 7:157201688 | ATAAGTAATTGCTTT[A/G]CTGTTCTGTGTTTTT | 9690 |
rs369260120 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170135 | TTTTTTTTTTTTTTT[-/C]TTTTTAACCATTTTT | 9690 |
rs369263915 | snp | G/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137844 | GCTGGGATTACCGGC[G/T]TGAGCGACCGTGCTC | 9690 |
rs369266654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243111 | ATCATATTGTGGCTC[A/G]ATCGCTGGAAGCCAC | 9690 |
rs369294698 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167698 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 9690 |
rs369300794 | snp | A/G | 0.000197853 | 0.00994422 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220720 | TGCCAGCATCCAGAC[A/G]TGTGTGGAGGTTCCG | 9690 |
rs369332981 | snp | A/G | 3.46693e-05 | 0.00416334 | intron-variant | UBE3C | GRCh38.p7 | 7:157220818 | TGAGGTATGAATTAC[A/G]TGCTGTCAAATTCAC | 9690 |
rs369346435 | snp | A/G | 0.00230628 | 0.0338795 | intron-variant | UBE3C | GRCh38.p7 | 7:157187038 | CAAGTGTCCGTGGGC[A/G]TCTGTGCCAGGGGGT | 9690 |
rs369375449 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178707 | TGCTGCAAAACTGTA[A/G]TGATGACAGTTTGAA | 9690 |
rs369380173 | snp | A/G | 1.67556e-05 | 0.0028944 | intron-variant | UBE3C | GRCh38.p7 | 7:157248323 | TCTTTGTTTGTAGAA[A/G]GCTTGTATATTCGAT | 9690 |
rs369409449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185189 | TGTGGGCTTTCTCAG[C/T]GAGAGAGAGGACAGG | 9690 |
rs369411959 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175159 | TTTTTTTTTTTTTTT[G/T]AGGTCATGGACTTCT | 9690 |
rs369417842 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259610 | CACTGTGCTAAGTGA[A/G]CGAAGCAAGACACAA | 9690 |
rs369435744 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160679 | CCCTTGTTAATTGAT[C/G]TATATCTTGAGAGAT | 9690 |
rs369454211 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180581 | TTTAATGTGCTACCA[-/TT]AATACGCTTGTATAT | 9690 |
rs369468087 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153726 | GTTAACTTTTCCTCC[C/T]GGCACTCTGGGAGGC | 9690 |
rs369468948 | in-del | -/AATGTGGTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192744 | CTGATGAATGTGGTG[-/AATGTGGTG]CTGGAGTGTTTATGG | 9690 |
rs369489495 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231886 | GACTATTAGTTTAAT[A/G]GGACTGCCGCAACAA | 9690 |
rs369489682 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200286 | TGGATATCTCAAAAT[A/G]CATTACATTAAAATA | 9690 |
rs369552384 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172047 | TTTTTTTTCCTTTTT[G/T]AGACGGAGTCTTGCT | 9690 |
rs369631343 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157255971 | TAGTACTAGACACCC[A/G]TTGTCTGTCATGTTA | 9690 |
rs369650562 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260494 | CCTGTGTGGTGGCAG[-/AG]TCTGGAGGGCTTGCT | 9690 |
rs369672815 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235781 | TTCCCTTACATTACT[C/G]TCTGTGTGGAAATTC | 9690 |
rs369675419 | snp | C/T | 3.51364e-05 | 0.0041913 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267777 | TGCTGGGGTCAGACC[C/T]CTACAGAGAACCAGT | 9690 |
rs369694982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159959 | AGCAGCGTAGCGTCT[C/T]GTATTCTTTTGTTGT | 9690 |
rs369707398 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163388 | AGAGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 9690 |
rs369743714 | snp | A/G | 1.76593e-05 | 0.00297142 | intron-variant | UBE3C | GRCh38.p7 | 7:157170490 | TGTCCTCGTTTACAC[A/G]TGTTCTGCTTTTTTG | 9690 |
rs369748919 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248391 | TGAGAACATGCTGGT[A/G]GAGCTGCCCTTTGCA | 9690 |
rs369753461 | snp | A/G | 5.24315e-05 | 0.00511986 | intron-variant | UBE3C | GRCh38.p7 | 7:157139345 | AGCAGGAAGGTGAGG[A/G]CCGGGCTGGCGGGGC | 9690 |
rs369791733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163530 | AGCACCAGTCTTACT[A/C]AACATTTCCCCAGTT | 9690 |
rs369800896 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137124 | TTGGTATTTTTAGTA[G/T]AGACGGGGTTTCACT | 9690 |
rs369820166 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182250 | GCACTGTTGTTAATA[A/G]AGAGTAGATGTTCAA | 9690 |
rs369821950 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203675 | ATTAAATTATTAATA[A/C]TATTTTATGATAGGG | 9690 |
rs369823901 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228157 | TCGTTGTCTTATCTC[C/T]GAACGATTCTCTGCA | 9690 |
rs369833073 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267495 | GGTAACTTTACTGAT[A/T]GGAGCAGGCACATTT | 9690 |
rs369839802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187157 | TTCTACTGTCCAAGC[A/G]TTTCATAAAAAATAA | 9690 |
rs369869117 | snp | C/T | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186847 | AGGAGGATGGCAGAC[C/T]GTCAGTATCATACAT | 9690 |
rs369877734 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175852 | TGTATACATTCTTTT[G/T]GTGAAGCAGGAGTTT | 9690 |
rs369897561 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138322 | CATATTTATATGTAT[C/T]GATGCTGTATCTATA | 9690 |
rs369945925 | snp | C/T | 4.94442e-05 | 0.00497188 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248576 | ATGACCTGGGAGAGG[C/T]GCAGGTGAGGGGTCA | 9690 |
rs370029145 | snp | A/G/T | 0.000148686 | 0.00862118 | intron-variant | UBE3C | GRCh38.p7 | 7:157256892 | TTTGCATTTCATAAA[A/G/T]CATGTGTTCATTTTG | 9690 |
rs370035047 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157609 | AGACATTACTGACAC[A/G]TTTGCAAGGATATCC | 9690 |
rs370047196 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236893 | TCCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 9690 |
rs370064813 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197858 | ATCAATAAGAACAAC[C/T]GCGTTAAGTATTGAT | 9690 |
rs370067574 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262645 | AGGCTGGTCTCGAAC[C/T]CCTGACCTCCGGTGA | 9690 |
rs370088775 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157156467 | GCATGTCACCACCCC[C/T]GGCTAATTTTTGTAT | 9690 |
rs370111750 | snp | G/T | 4.95814e-05 | 0.00497878 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254110 | GTCGTCAGCCTCGAG[G/T]GGCTCCGAATGTTTG | 9690 |
rs370142937 | snp | C/G | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174931 | CAGATATGGCTGTAT[C/G]AGAACTTAATTAAAC | 9690 |
rs370210251 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195800 | ATGGGTTGTGACTTT[-/T]GAGCACCTATGAGTG | 9690 |
rs370217595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188671 | AGGCTTGATTTTATG[A/T]GTACAGCACCTATTT | 9690 |
rs370244354 | in-del | -/AAAACCAT | 0.344815 | 0.231323 | intron-variant | UBE3C | GRCh38.p7 | 7:157180582 | TTAATGTGCTACCAA[-/AAAACCAT]ATACGCTTGTATATG | 9690 |
rs370251664 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225455 | GAAGTTCAAGGAGAT[A/G]GTCCATTTCTGGATG | 9690 |
rs370262523 | snp | A/C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268615 | TGTCCCGATGCTAGC[A/C/T]GTGCCGGTCTCCCAT | 9690 |
rs370290968 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234694 | ACCTGACTTCACTAC[C/T]GTAACGGTATGTGTT | 9690 |
rs370316043 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157150653 | GTATTAATGTCTGTC[A/T]TTAATTTATTAACAT | 9690 |
rs370374719 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176067 | CAAAACACCTTTAAC[A/G/T]TAACTTTTGAATGTA | 9690 |
rs370379864 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154394 | AATCCCCTAACTTCC[A/C]ACCATTATTTTCTCA | 9690 |
rs370380195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157169565 | ATTGTTAGTAGAGTC[A/G]GTGTTTTGCCACGTT | 9690 |
rs370380478 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248606 | AGGAGGAGGATTCAC[A/T]TACCTGTATAGCAAG | 9690 |
rs370399641 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209603 | AATATTTGATTAAAC[C/T]CTGGGGTCTTTGTTA | 9690 |
rs370403608 | snp | C/T | 1.65798e-05 | 0.00287917 | intron-variant | UBE3C | GRCh38.p7 | 7:157248631 | AGCAAGTAGCAGCAT[C/T]TCCTTGTGTGTGGAA | 9690 |
rs370407477 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160329 | ATCTGCCGGCCTTGG[C/T]CTCCCAAAGTACTGG | 9690 |
rs370416956 | snp | A/C | 3.36134e-05 | 0.00409946 | intron-variant | UBE3C | GRCh38.p7 | 7:157183834 | TTTCCATTTTAAAAA[A/C]TAATGTTTAACTAAA | 9690 |
rs370448076 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197199 | CAAATTTTCAACTTA[C/T]TTGATCAAAAGATTT | 9690 |
rs370465544 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138585 | ACCCCATCCCGGCCC[A/G]TGCCTCGCACTCCAC | 9690 |
rs370474274 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158441 | GTGGCAGGACCGGTG[C/T]AGAGAACACTGCATC | 9690 |
rs370503285 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE3C | GRCh38.p7 | 7:157163868 | GAAAGAGAGAGGTAA[A/G]AACAGTTTTGTAATA | 9690 |
rs370521863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260887 | AATAACGTGTGCCTA[C/G]GAGTGCGAGAGCCTT | 9690 |
rs370528507 | snp | C/G | 0.000347939 | 0.0131852 | intron-variant | UBE3C | GRCh38.p7 | 7:157207346 | TAATTAGTTCCCAAA[C/G]TAAGACTAATTTTAA | 9690 |
rs370567663 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157204497 | AGCTTATCAGGTAAT[C/T]GAGGTACAGATGGTT | 9690 |
rs370588602 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245007 | TAACCTGTGTTTAGA[A/C]AATACCTTGATTTAT | 9690 |
rs370602326 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202046 | GTAAGTTTCCTTTAA[A/T]CATCCTAGCCATGTT | 9690 |
rs370602625 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178767 | TATTTTCGTCTGAGA[A/G]TACTTACTTGCCTGT | 9690 |
rs370613140 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157187667 | TGTAGGCTCTGCCCC[C/G]CTGGGTTCATGCCAT | 9690 |
rs370620880 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254012 | GCGCCAACCGGATTG[C/T]GTACATCCACTTGGT | 9690 |
rs370629644 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264444 | TACTACAGGTGTGAG[C/T]CAACATGCTCGGCCT | 9690 |
rs370657959 | in-del | -/AAGAGCCTCCT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190323 | TCTTAAGAGCCTCCT[-/AAGAGCCTCCT]CTTTCTGTCCCTGTT | 9690 |
rs370700020 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185989 | ATTCATATATACACA[A/T]ACATATGAAAAAAGT | 9690 |
rs370712043 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219491 | AACCTCTACATCTAA[C/G]TACAAAATTACAGGA | 9690 |
rs370716614 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162163 | ACTACTCTCTGACAC[C/T]GTTCTGATAAAGTAT | 9690 |
rs370761071 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150390 | TCTCAAAAAAAAAAA[-/A]GAGTCTAACAAGATA | 9690 |
rs370796468 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183935 | TGCAGACCTTCCTCT[C/G]TCAGTTACCAGTCTC | 9690 |
rs370843256 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254402 | TAATTAATTTATTTA[-/T]TTTTTTTTTTTTCAG | 9690 |
rs370847816 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165958 | ATGCTTTTAGAATTC[A/G]GTCTTTATCTTTGAC | 9690 |
rs370871173 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177304 | GATGGCTCTTTTTCA[A/G]GAGTCTGTTCAAATC | 9690 |
rs370876429 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237485 | GTTTAGCACCACAAG[A/G]TAAATTCTTTCTGCC | 9690 |
rs370888683 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198670 | CTCCTGAGCAGCTGG[-/G]ATTACAGGCATGCGC | 9690 |
rs370895018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157167074 | AGCTGGGATTACAGG[C/T]GTGCACCACCATGCC | 9690 |
rs370957160 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201797 | TCCATGTCAACACGG[A/G]TGATCACAGGGTATG | 9690 |
rs370957217 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157208054 | GTTTTAATTTGCAAG[A/T]CTTTTTTTTTTTTTT | 9690 |
rs371009799 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157144037 | GAGTCCACTGACTGC[A/G]GAGCTGGGAAGAATT | 9690 |
rs371016187 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241212 | GGACTGCTGAGTGTC[A/G]CAGCATAGTCAGGAA | 9690 |
rs371022412 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234785 | TTGATTTGTGAGTTG[A/G]CTTTGGTGGCAGTTT | 9690 |
rs371024243 | in-del | -/TTTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232352 | TTGTTTGTTTGTTTG[-/TTTG]AGACGGAGTCTCTCC | 9690 |
rs371036319 | in-del | -/G | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139801 | CATCAGGGAGTGGCT[-/G]GCTTTTCGAATGCCA | 9690 |
rs371056792 | in-del | -/CC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154083 | CAGCACCTTGGGAGG[-/CC]GAGGCCGAGGTGGGT | 9690 |
rs371060403 | snp | A/G/T | 5.56726e-05 | 0.00527572 | intron-variant | UBE3C | GRCh38.p7 | 7:157182058 | TTAATCAGTGATTGG[A/G/T]TGGACAGTATAATTT | 9690 |
rs371069002 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157176827 | GCCTGGGGCTGTTTT[C/T]TCTAAGGAGCACTGA | 9690 |
rs371072828 | snp | C/T | 0.000247735 | 0.0111268 | intron-variant | UBE3C | GRCh38.p7 | 7:157184038 | AAGCCCGGTAAGCCC[C/T]GTGCCCTGCATCTGG | 9690 |
rs371104534 | in-del | -/TAAAA | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267965 | GCTTTTCAAATAACT[-/TAAAA]TAACACGTTATGTGC | 9690 |
rs371181410 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264420 | TTACACACACACACA[C/T]ACACCTGGTACTACA | 9690 |
rs371181663 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157265590 | CAACACGTCGTGCCG[C/T]GCGTGTGCATGGAAC | 9690 |
rs371191013 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187574 | TGTGTGTGTGTGTGT[-/GT]TTGTTTTTTGTTTTT | 9690 |
rs371192489 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202402 | TGGCTCACGCCTGTA[A/G]TTCCAGCACTTTGGG | 9690 |
rs371198400 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169318 | TAAATAATAAAATAC[A/T]AACATGGGCCTCACC | 9690 |
rs371202534 | snp | A/G | 6.90978e-05 | 0.00587742 | intron-variant | UBE3C | GRCh38.p7 | 7:157223383 | CTTTATTGTCACTAC[A/G]TATCATATTAGTGTT | 9690 |
rs371210548 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138440 | ATAGAACAGGTGGGA[C/T]GTAAACAGACGGGCT | 9690 |
rs371215767 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | UBE3C | GRCh38.p7 | 7:157207692 | ATAGAAAACTGGATT[C/G]TGTTTTTTAGTTGTA | 9690 |
rs371216712 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150767 | TATCTGAACAGTAAA[A/G]ATAGCTAGTTTCCCA | 9690 |
rs371220656 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157211479 | AATATGTGCTGAAGA[A/G]TACTGTTTTTCAAAA | 9690 |
rs371238850 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243064 | ATCTCAAAAAAAAAA[-/A]GGAAGCGTCAACTCC | 9690 |
rs371243377 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221509 | GCACTTTAGGAGGCC[A/G]AGGTGGGCGGATCAT | 9690 |
rs371249151 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238985 | GAGAAGTGGCCATGT[C/T]ATTTAGCACTCTGGA | 9690 |
rs371273857 | snp | A/G | 3.48742e-05 | 0.00417563 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170310 | TTCTTCCAGTATTCC[A/G]TCCAAAGAAGTGCAT | 9690 |
rs371283480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157144384 | GGAAATTCGGTGTCT[C/T]GGAAATAGTTTTGTC | 9690 |
rs371300314 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262409 | AGTCTCTTCATAGGC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs371301343 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230976 | TATGTTAAAATGTCC[C/G]TAAGATCCTCACACC | 9690 |
rs371336791 | snp | A/G | 3.29815e-05 | 0.00406075 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207402 | TTTAATTCAAGGTCT[A/G]TGGTACCGTTGCTTC | 9690 |
rs371374726 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200990 | TTGTATTTCAAGAAA[-/A]GTGACTTGAGTCCGT | 9690 |
rs371391259 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162116 | TGAATATTGTTAGTT[C/G]ATGTATCAGTGTATA | 9690 |
rs371437286 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195223 | TTTCCAGGAAAGATA[C/T]GTGAGGAGCCTCCTG | 9690 |
rs371458347 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191854 | ATTTTGGAAAAAATA[C/T]TGAGGATGTGCCTGG | 9690 |
rs371459838 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158528 | GCTGCCAAAGCTGTG[A/G]TTAAAAGTGATGATT | 9690 |
rs371465790 | snp | A/G | 1.77087e-05 | 0.00297557 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267787 | AGACCCCTACAGAGA[A/G]CCAGTGCTTCCTTCG | 9690 |
rs371467962 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157237372 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 9690 |
rs371470757 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234531 | GCCTTGTTAAGCAGG[A/G]ATAATGGGAAGGAAT | 9690 |
rs371493097 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228156 | CTCGTTGTCTTATCT[C/T]CGAACGATTCTCTGC | 9690 |
rs371518577 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245151 | CTCTGAAGGTTTAAA[C/T]CTGCCTCATGTAAAA | 9690 |
rs371525696 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262534 | AGTGATTCTCCTGCC[A/G]CAGCCTCCCGAGTAG | 9690 |
rs371531304 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157206950 | TGAATAGCTTTCAAC[-/G]TTACCAAAAGTTAAG | 9690 |
rs371651989 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148299 | GTAGAGATGGGGTTT[C/T]GCCATGTTGTCCATA | 9690 |
rs371653327 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177700 | CCTGCCCAGCCTGCC[C/T]GCTGGGTCCTCACCC | 9690 |
rs371662009 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253271 | TACAAGTGGGGGACA[A/G]TAAGACCCAGGTCTG | 9690 |
rs371670816 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170525 | AAGTGGAAATGGCTT[C/T]TCATCAGAAAGTTAA | 9690 |
rs371697523 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189636 | CTGGCCTTTGTGTGT[A/T]TTTCACATTCCTCGT | 9690 |
rs371706917 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239850 | GAGGTAGAGGAACAC[-/T]GGGTGCAGCTGCATG | 9690 |
rs371718321 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244769 | CCTTTTTATTTCAAA[C/T]CATTTTGGCACAATT | 9690 |
rs371782525 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174278 | AAGGCATGAGACTTA[C/T]GCCTAATATATGAGA | 9690 |
rs371816946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217832 | ATAAGAGCGAAATTC[C/T]GTCTCAAAAAAAGAA | 9690 |
rs371868065 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166945 | GTGGTGGTGGTGGTT[G/T]TTGAGACAAAGTCTT | 9690 |
rs371869370 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219137 | CCACTCCAGGTGCAG[C/T]GCATGTCTAGGGTCT | 9690 |
rs371870345 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268055 | ATCTCAGTGAAATTA[A/T]CCAAAGATGAAGCTT | 9690 |
rs371885499 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198551 | TTTTTTTTATTTTTT[C/T]CGACAGGGAGTCTTG | 9690 |
rs371895888 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181598 | TTATCTCGAGTTCCT[A/G]TAGCAAAAATTTTGC | 9690 |
rs371913751 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242520 | GCCTGAGTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 9690 |
rs371980545 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230152 | GACCTCAAGGCGATC[C/T]GCCCACCTCAGCGTC | 9690 |
rs372002350 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253895 | TTGTTTCTTGCTTTT[C/T]TTTTTAACCTATTAT | 9690 |
rs372041598 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163086 | CATATGCAGCTGTTA[A/G]AAATGATACCCAGAG | 9690 |
rs372044414 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227711 | CTCAGAAAAAAAAAA[A/G]AAAAAACTACTCCCT | 9690 |
rs372047038 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154578 | TCCATAGCATAGTTT[A/G]ATACTTAATATAACC | 9690 |
rs372050332 | snp | A/G | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181566 | GCAAGCTTCCATCAA[A/G]TATTGAATATTCTGA | 9690 |
rs372100576 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154965 | CATAGTCAGTTTTTT[C/T]CCCCATCTTTGTGAT | 9690 |
rs372104746 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261675 | ATAAATAGCAAAGGC[A/G]GGCAGGCATAATTTT | 9690 |
rs372163132 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210380 | CCCAAAATAAAAATC[-/A]ACTGCATAATTTTTG | 9690 |
rs372170201 | snp | A/G | 6.80492e-05 | 0.00583266 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170446 | ATGAAGACTCAAAAC[A/G]TTTGGTGAGTGTTAA | 9690 |
rs372172262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157262450 | TTGAGATAGAGTTTC[A/G]CTCCTGTTGCCCAGG | 9690 |
rs372187177 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266271 | GTAAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 9690 |
rs372209828 | snp | C/T | 0.000784045 | 0.019784 | intron-variant | UBE3C | GRCh38.p7 | 7:157184079 | TGCAGGCAGCCCCGT[C/T]GGATCTTCTAGCTTT | 9690 |
rs372214410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152361 | TAGGTTTTAGAGATG[C/G]GTGGGGGGCAGTTTG | 9690 |
rs372216275 | snp | C/T | 3.32779e-05 | 0.00407895 | intron-variant | UBE3C | GRCh38.p7 | 7:157231059 | ATCTTTCCTCCTCAC[C/T]CTCCCATTTTTTTTT | 9690 |
rs372228276 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142460 | AGTAATTGCTACATT[C/T]TAAATTTCCCTTGGT | 9690 |
rs372262069 | in-del | -/GA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211168 | TTATCCATATGTCTG[-/GA]GAGAGAGAGAGAGAG | 9690 |
rs372266207 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172040 | ATCTTTTTTTTTTTT[C/T]CTTTTTGAGACGGAG | 9690 |
rs372280361 | snp | A/G | 3.52796e-05 | 0.00419983 | intron-variant | UBE3C | GRCh38.p7 | 7:157254356 | AAAATGTTGCAGGTG[A/G]TCATATTTCCAAAGT | 9690 |
rs372299003 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206096 | AGTGTCTGTTAACCT[A/G]TGATTGATTTGACTT | 9690 |
rs372303330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157196462 | TAGATCTAGTCTGTC[C/T]GACAGAATATACATT | 9690 |
rs372311235 | snp | A/G | 1.72934e-05 | 0.00294048 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207910 | GCATACAGATGGAAC[A/G]GAAAAGATGGATTCA | 9690 |
rs372311479 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210112 | AACCCGGGAGGCAGA[A/G]GTTGCAGTCAGCCGA | 9690 |
rs372311914 | snp | C/T | 1.78992e-05 | 0.00299153 | intron-variant | UBE3C | GRCh38.p7 | 7:157216843 | AGCTCACGTGTGTGA[C/T]GCGGATATGTTCTTT | 9690 |
rs372325626 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227050 | CTCCCACTTGACCCT[A/G]GAGGTCTTTACAGCT | 9690 |
rs372366217 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147194 | TTAATTTGTTTAGTT[A/C]TTTTATTTCTTTCAT | 9690 |
rs372366368 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164540 | AAGAAGGTAAAAGAA[A/G]GACACTAATGACATT | 9690 |
rs372374777 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234674 | AGGTTTGAGAAAGGG[C/T]TCCAACCTGACTTCA | 9690 |
rs372376326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266002 | TACCTCCCTCAATTT[C/T]GTCTTGTAATTTAAT | 9690 |
rs372378915 | snp | A/T | 5.0068e-05 | 0.00500315 | intron-variant | UBE3C | GRCh38.p7 | 7:157254189 | TTGTCACAGGAAATG[A/T]ACAGGCTTTCTTAAA | 9690 |
rs372378967 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218575 | AAGCCTGTTGCATCT[A/G]ACTCTGCCCACTGAC | 9690 |
rs372396348 | snp | C/T | 4.94401e-05 | 0.00497168 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182300 | CTGGCTTTTCTATTT[C/T]GTTTTAACTGTTGGC | 9690 |
rs372403358 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238300 | GAGGGCAGCAGAATC[C/T]GGCCTGTGTTGTCGT | 9690 |
rs372438226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188464 | CCTTAGCTCTTTGCC[A/G]GCTAATTGCATGAGA | 9690 |
rs372487419 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160231 | AGGTGCGCGCCACCA[C/T]GCCCAGCTGATTTTT | 9690 |
rs372488996 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193920 | TTAATTCTCTCCTAA[C/T]GTAAATCTCTATTTT | 9690 |
rs372529777 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204215 | TAAAATGAAATAACT[C/G]ATTTTCTGAAACTGG | 9690 |
rs372529835 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | UBE3C | GRCh38.p7 | 7:157183866 | TACGTTTTAACTGAT[A/T]GTTTTGCAAAGGGGC | 9690 |
rs372537696 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172109 | GCGATCTCAGCTCAC[C/T]GCAACCTCGCCTCCT | 9690 |
rs372540671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232872 | TGCTTTTAGGACTTC[C/T]TTTACATAACAGTTT | 9690 |
rs372541846 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190700 | TGCATTCTCTTGAAC[A/T]GTGTAGACTCCCTTT | 9690 |
rs372547823 | snp | C/T | 1.65151e-05 | 0.00287355 | intron-variant | UBE3C | GRCh38.p7 | 7:157257088 | AAGACCACTTCATAA[C/T]AAGAAAGGCAGCAGA | 9690 |
rs372614185 | snp | C/T | 1.65345e-05 | 0.00287524 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220758 | GGGAGGATAGGCCCG[C/T]TGCAGTCCACCCTGG | 9690 |
rs372622033 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222314 | TCTTTCAAGGAGGAG[A/G]AGTTTTAAATTTTGA | 9690 |
rs372646773 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192767 | GTTTATGGCAAGTCA[C/G]TTTGACAGACATTAT | 9690 |
rs372655327 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176505 | GTCTCAAACTCCTGA[C/T]CTCAGGTCATCCGCC | 9690 |
rs372668340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250094 | TGTGGTGAGAACAGG[A/G]GCAGGAAGTGGGGCT | 9690 |
rs372724666 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157661 | GCCAAAAACTGAAAA[A/C]AACCTAAATGACCAT | 9690 |
rs372775416 | snp | A/C | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216907 | TGAAGTCCAGAGACA[A/C]GAGGAGAAATTTTTG | 9690 |
rs372803338 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209203 | GCTTATTCATCCTCC[-/C]AAGTCCACGAGAGTC | 9690 |
rs372897199 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205370 | ATATAAGAATTTTAT[A/G]CATCCTGCAATATGT | 9690 |
rs372919865 | snp | C/T | 0.000161987 | 0.00899818 | intron-variant | UBE3C | GRCh38.p7 | 7:157139360 | GCCGGGCTGGCGGGG[C/T]GCCCTCGGCTCGGGG | 9690 |
rs372933304 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157170231 | TGTAAACACAGCAAC[A/G]TATATTTACATCATA | 9690 |
rs372957308 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194190 | AATGGGGCTGGCTGT[G/T]ATACATTATACAGGT | 9690 |
rs372972761 | in-del | -/CT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189829 | TTTGTGACGGAGTCT[-/CT]TGCCTTGTCGCCCAG | 9690 |
rs372997452 | snp | A/T | 1.64893e-05 | 0.0028713 | intron-variant | UBE3C | GRCh38.p7 | 7:157248589 | GGCGCAGGTGAGGGG[A/T]CAGGAGGAGGATTCA | 9690 |
rs373005806 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137510 | GACCTGAGGTGATCC[A/G]CCCACCTTAGCCTCC | 9690 |
rs373038546 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262409 | AAGTCTCTTCATAGG[C/T]TTTTTTTTTTTTTTT | 9690 |
rs373070421 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192344 | CCTTTTCGATCCGCC[A/G]TCTGCGGTGGAGCCG | 9690 |
rs373077672 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251884 | TCACGGCTGTAATCC[C/T]AGCACTTTGGGAGGC | 9690 |
rs373114150 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197397 | CTTCAACTAAAAACT[C/G]AAACATACTTATCTT | 9690 |
rs373128578 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157197052 | ACAAGGCAAAACTGT[C/T]GTTTCTGATACTAGT | 9690 |
rs373155122 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241686 | TTGGACCCAGCAAAC[A/G]TATTTACCCAAAAAC | 9690 |
rs373170556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157237661 | TGTTAATTTGTCACC[A/G]TGAAGATTAGAAGCA | 9690 |
rs373200702 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187668 | GTAGGCTCTGCCCCC[-/C]TGGGTTCATGCCATT | 9690 |
rs373229004 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149273 | CTTGGTCAGGCTGGT[C/T]TCGAATTCCTGACCT | 9690 |
rs373266605 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265196 | ACCTCTCAGAGAGTT[C/T]CGTGTACACGTGTGC | 9690 |
rs373293168 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187573 | TTTGTGTGTGTGTGT[-/GT]TTGTTTTTTGTTTTT | 9690 |
rs373370776 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224421 | GGATGGTCTCGATCT[C/G]CTGACCTCGTGATCT | 9690 |
rs373435492 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206695 | CTGGGCTCAAGCCAT[G/T]CTCCTGCCTCAGCCT | 9690 |
rs373436674 | in-del | -/A | 0.36315 | 0.222928 | intron-variant | UBE3C | GRCh38.p7 | 7:157230395 | GCTGATAAGCTTTTG[-/A]AAAAAAAAAAAAAAT | 9690 |
rs373446282 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200024 | TCATGGCGTGTGACT[A/G]ATAAACATCATGCAT | 9690 |
rs373465870 | snp | C/T | 3.30186e-05 | 0.00406303 | intron-variant | UBE3C | GRCh38.p7 | 7:157201710 | TGTGTTTTTCTCCTA[C/T]TCCTTTTTAGGCTTC | 9690 |
rs373497436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156487 | AATTTTTGTATTTTT[C/G]ATAGAGACAGGGTTT | 9690 |
rs373520723 | snp | C/T | 3.30229e-05 | 0.0040633 | intron-variant | UBE3C | GRCh38.p7 | 7:157256895 | GCATTTCATAAAGCA[C/T]GTGTTCATTTTGCCA | 9690 |
rs373522013 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220049 | AACCCCATCTCTACA[A/G]AAAGTACAAAAATTA | 9690 |
rs373556735 | snp | A/G | 3.63788e-05 | 0.00426475 | intron-variant | UBE3C | GRCh38.p7 | 7:157188983 | AGACCTTTGTACCCT[A/G]ACATGGAAAGATTTC | 9690 |
rs373633261 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157211291 | TAAAGCAACAGCAGT[G/T]CCCTGTTAATATAAT | 9690 |
rs373648534 | snp | C/T | 0.00017138 | 0.00925529 | intron-variant | UBE3C | GRCh38.p7 | 7:157174870 | ATGTAAATTAGCAAA[C/T]TATTAAATTTTCATT | 9690 |
rs373650954 | snp | A/C/G | 3.32454e-05 | 0.00407698 | intron-variant | UBE3C | GRCh38.p7 | 7:157178867 | GTAGTAGGCAGGATC[A/C/G]GAACTGTGGCTCAGC | 9690 |
rs373651251 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198595 | GCTGAAGTGCAGTGG[C/T]GCCATCTCGGCTCAC | 9690 |
rs373663046 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250737 | AATTTGGCGGGGGGG[-/G]CTGTTACTGTCATTA | 9690 |
rs373664428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205760 | AAACATGGATCATGT[A/G]TGCTCAGGTTGTGTA | 9690 |
rs373693241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224653 | AGATTACTTGGTTCC[A/G]TTCTTCAGTAATGGC | 9690 |
rs373720494 | snp | A/T | 3.29902e-05 | 0.00406128 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225477 | TTCTGGATGGAATTA[A/T]TGTCACAATAAGAAG | 9690 |
rs373749771 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231918 | TTACCACACTCTTTG[G/T]GGGGGGAGGGAGGCT | 9690 |
rs373801466 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264275 | TGGTACTACAGGTGT[A/G]AGCCAACATGCTTGG | 9690 |
rs373829120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261949 | TTCAGTGAAGAACTT[C/T]ATTTTTTTACTTTTA | 9690 |
rs373835175 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252326 | ACATTGAAATATAAT[A/T]GCTAGCCTCCTGAGG | 9690 |
rs373868761 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163114 | GAGATGGCCGGGCGC[A/G]GTGGTTCACGCCTGT | 9690 |
rs373894937 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217730 | TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 9690 |
rs373903995 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153442 | GTTGTATTGCGTAAT[A/G]GGAGAGTCACAATTC | 9690 |
rs373926824 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137565 | GCCAGGACTGTATTT[C/T]TTTTTTTTTTTTTTT | 9690 |
rs373980802 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157236411 | TCAGATTATTTGATA[-/T]GATCTTGGTTATATA | 9690 |
rs373988071 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151407 | AGTTCACTCGGAGAA[G/T]ATTGTATAGCTCTTT | 9690 |
rs374015092 | snp | A/G | 8.23676e-05 | 0.00641693 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182256 | TTGTTAATAGAGAGT[A/G]GATGTTCAAGAAAGA | 9690 |
rs374091013 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157169591 | ACGTTGACCAGGCTG[A/G]TCTGGAACTCATGAC | 9690 |
rs374155674 | snp | A/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231895 | TTTAATAGGACTGCC[A/G/T]CAACAAATTACCACA | 9690 |
rs374160304 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248442 | GCTTGGAACCAGTGC[C/T]GACGTGGACATTCAC | 9690 |
rs374166109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241528 | GCTGCCGCGCACACC[C/T]GCGAGTACGGCGGGA | 9690 |
rs374180752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167626 | CACTGCAAGCTCCAC[C/T]TCCCGGGTTCACGCC | 9690 |
rs374183197 | in-del | -/GTTT/GTTTGTTT | 0.0759484 | 0.182396 | intron-variant | UBE3C | GRCh38.p7 | 7:157232351 | CAGGAATTGTTATTA[-/GTTT/GTTTGTTT]GTTTGTTTGTTTGTT | 9690 |
rs374198589 | snp | C/T | 8.23716e-05 | 0.00641709 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183962 | TCTCTCCTGCCAGCG[C/T]GAGCTGTCACGACTC | 9690 |
rs374201495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157168503 | ATGAATGTTCATAGC[A/G]GCCTTAATTCATAAT | 9690 |
rs374214647 | snp | C/T | 0.00039741 | 0.0140907 | intron-variant | UBE3C | GRCh38.p7 | 7:157163897 | TACTCTGTAGATAAG[C/T]ATTTTTTCTACAGCA | 9690 |
rs374216652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157221365 | CCAGGGTGGCTGCAC[A/G]GCTTTGCATTCAGAC | 9690 |
rs374222544 | snp | G/T | 1.70755e-05 | 0.00292189 | intron-variant | UBE3C | GRCh38.p7 | 7:157225570 | TCTGTGTATTATTTG[G/T]CAGGTGGAGGCTAGG | 9690 |
rs374224837 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182487 | GGCAGTGTGTTCCTG[C/G]GGACAGTTTCCAGAT | 9690 |
rs374235398 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157989 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 9690 |
rs374235935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157253028 | TGAGCCACTATACCC[A/G]GCCTGTTTTTTTGGT | 9690 |
rs374260046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157223885 | AGATCGTGCCAGTAC[A/G]CTCCAGCCTGGGCAA | 9690 |
rs374262098 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204439 | GCTTCTCTGTTCCTG[C/T]CCTAAGACTTGGGTT | 9690 |
rs374306130 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187725 | GGGACTACAGGCGCC[C/T]GCCACCTCGCCCGGC | 9690 |
rs374306761 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237893 | CTCTACCACTAAAAA[A/G]AAAAAAAAAGTAGCC | 9690 |
rs374316908 | snp | C/T | 4.99563e-05 | 0.00499756 | intron-variant | UBE3C | GRCh38.p7 | 7:157254174 | CTTTCTGGGACACGC[C/T]TGTCACAGGAAATGA | 9690 |
rs374340479 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166599 | TACAAAATTACCCAG[A/G]CATGCTGGCGCATGC | 9690 |
rs374344372 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228530 | GGTTGGTTACTTTTA[C/T]TTTATTTCATTTAAT | 9690 |
rs374344669 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197748 | TGTACAATAAAGTTC[C/T]GGACATCCAGGATCC | 9690 |
rs374348336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244398 | TTGCTATTAGTATAC[A/G]TTCTTATTTTATGTT | 9690 |
rs374382357 | snp | C/T | 3.32469e-05 | 0.00407705 | intron-variant | UBE3C | GRCh38.p7 | 7:157163775 | TTAAAATTGAAATTA[C/T]AACCTTACCTCCTTT | 9690 |
rs374420490 | in-del | A/GG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154004 | CCTGTCTGGGGGGGG[A/GG]AAAGTTAACTTTTTC | 9690 |
rs374438325 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234894 | CATAATTCATTGTAT[A/G]AAAATCTTTACAATG | 9690 |
rs374453720 | snp | C/T | 0.000501588 | 0.0158285 | intron-variant | UBE3C | GRCh38.p7 | 7:157254200 | AATGAACAGGCTTTC[C/T]TAAAATTTACCTCAA | 9690 |
rs374462803 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191769 | CAGAAAAATACAGAT[C/T]TGTTTTTCATTGTAT | 9690 |
rs374471671 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157158529 | CTGCCAAAGCTGTGA[A/T]TAAAAGTGATGATTA | 9690 |
rs374480780 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226303 | AAAGGAGAATTATAC[C/T]GTGATAGCATTTGGA | 9690 |
rs374507232 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219146 | GTGCAGCGCATGTCT[A/G]GGGTCTGCTGGTCTG | 9690 |
rs374513542 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246334 | CTCACAGTTGAAACG[C/T]TTCTCCTTTGCTGGA | 9690 |
rs374521266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202281 | TTAACTGAGTATGTA[A/G]TAGGTAGGAATTTCA | 9690 |
rs374527003 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168641 | TGAAGTTCTCACATA[A/T]GCTGTAACATAGGTG | 9690 |
rs374536496 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140131 | CTGGAACCGCTAAGT[C/T]GTTGAACACTGTGTG | 9690 |
rs374543621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154226 | CTTGGGAGACTGAGG[C/T]GGAGAATTGCTTGAA | 9690 |
rs374586429 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260903 | GAGTGCGAGAGCCTT[A/C]TCCACCTCCGTGATG | 9690 |
rs374605882 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239512 | ACTAAGTGCTTTTCC[-/A]TAAGTGTGTTCACTG | 9690 |
rs374612885 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209851 | TTATGCCTCAAAATG[A/T]CTCCCTGCCACTTTA | 9690 |
rs374640473 | snp | G/T | 0.000645989 | 0.0179604 | intron-variant | UBE3C | GRCh38.p7 | 7:157225357 | ATTCTTTGGTAGGTT[G/T]TAAGAGGTCTTTTGT | 9690 |
rs374658982 | in-del | -/GATT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161437 | AGTATCTGGAGGATT[-/GATT]AATTTCTTTGATTTT | 9690 |
rs374664394 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252085 | AGGTTGCACTGAGCC[A/G]AGATTGCTCCACTGC | 9690 |
rs374694439 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165142 | TCAACCAAGAAAGAT[A/G]TTTGTTGGTTGGTGT | 9690 |
rs374749167 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162558 | TTTTTTTTTTTTTTT[G/T]AGACAGGATCTTGCT | 9690 |
rs374775655 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226109 | TCTGCCCCTAAAATT[C/T]AGTTTGCAAGCTGTT | 9690 |
rs374782064 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209004 | CTTTGGGTCTTTTAT[C/T]ACTGCTTTTGTCAAG | 9690 |
rs374782094 | snp | A/G | 6.59272e-05 | 0.00574101 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207410 | AAGGTCTATGGTACC[A/G]TTGCTTCAGGTGATA | 9690 |
rs374783921 | snp | C/T | 7.16666e-05 | 0.00598566 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186944 | GAGGGACTCTGCGAG[C/T]GAGGAGGTCTTCACC | 9690 |
rs374804035 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187557 | TGGCTAATTTTTTGT[G/T]TTTGTGTGTGTGTGT | 9690 |
rs374809082 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221745 | GACTGTCTAAAAAAA[-/TT]AAAAATTTGGCCATT | 9690 |
rs374811556 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268897 | GCAGAGTGACCCTTT[G/T]CTGATGCTGGGGGGA | 9690 |
rs374858712 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140444 | GGTGATTGCTTGGAA[A/G]TCACTTGTGCTCCAG | 9690 |
rs374876730 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170463 | TTGGTGAGTGTTAAC[C/T]ACATTTTCACTTGTC | 9690 |
rs374920083 | snp | C/T | 0.000116611 | 0.00763492 | intron-variant | UBE3C | GRCh38.p7 | 7:157184076 | CGATGCAGGCAGCCC[C/T]GTCGGATCTTCTAGC | 9690 |
rs374923033 | in-del | -/T/TTTT/TTTTT | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157201658 | ttttttttttttttt[-/T/TTTT/TTTTT]AAGAAATGTTTTGAA | 9690 |
rs374994880 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229057 | CAAAGCCAACAGAGG[A/G]CAGCAGCGCATGGGG | 9690 |
rs375000090 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192030 | TTAAACATTTCAGCA[C/T]ATAGTGATCTTAAAA | 9690 |
rs375004167 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222566 | CTGGGACTATAGGCG[C/T]GTGCCACCATGCCCA | 9690 |
rs375004239 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157205701 | GCATTCATTCATTGA[A/T]GAATCTGTTCAGCAT | 9690 |
rs375017379 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268621 | GATGCTAGCCGTGCC[G/T]GTCTCCCATCATCCG | 9690 |
rs375023578 | snp | A/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249246 | ATTAGCAGGCTCCCC[A/C/T]ACCTCCCGCAGGCAG | 9690 |
rs375080353 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265781 | TTAAGACGCTGAAGC[A/G]TTGGTTGCCAGTGGG | 9690 |
rs375084890 | snp | C/T | 0.00016472 | 0.00907375 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267596 | TCAGGAGTTGTATCC[C/T]GCATTTTGTATTCAC | 9690 |
rs375090854 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213606 | TCTGAAAGTGAATGT[C/G]GAAAAAAGGAATGTG | 9690 |
rs375101984 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172042 | CTTTTTTTTTTTTCC[C/T]TTTTGAGACGGAGTC | 9690 |
rs375104549 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236500 | TAGAATTCAGTGTGC[A/C]TTTAATGTATTCTGT | 9690 |
rs375117361 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186293 | GCTGGGTGTGGAGGC[A/G]GGCAAGTCCCAGCTA | 9690 |
rs375131226 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158467 | GCATCTGTGCGTTGT[A/G]TTTAATCACAAAGGC | 9690 |
rs375153532 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178595 | TAATCTTGTACTGGA[A/T]TAGTTTCTTAACCAT | 9690 |
rs375186475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157163319 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 9690 |
rs375199811 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178769 | TTTTCGTCTGAGAAT[A/G]CTTACTTGCCTGTTT | 9690 |
rs375200996 | snp | C/G | 1.7364e-05 | 0.00294647 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207911 | CATACAGATGGAACA[C/G]AAAAGATGGATTCAG | 9690 |
rs375201873 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169911 | CTGATCTCGAACTCC[C/T]GACCTCAGGTGATCC | 9690 |
rs375273636 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217340 | TTTTTTTTTTGAGAC[A/G]GAATCTTGCTATGTT | 9690 |
rs375277308 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186836 | TGGTATGTTCTAGGA[C/G]GATGGCAGACTGTCA | 9690 |
rs375283546 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199059 | CTCATTTTTGTTTCT[A/G]TGTCTACACACAAGG | 9690 |
rs375283665 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214318 | TAATTTGATAATGTT[C/T]GTAATCTGTAGAAAA | 9690 |
rs375294435 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180035 | TTGTTTTCTAAAATT[A/G]TAAGGAAGATATTTA | 9690 |
rs375305049 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230447 | ACGCCTGTAATCCCA[-/A]GCACTTTGGGAAGCC | 9690 |
rs375345050 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173507 | GGGTTTTCAAAGTTA[C/T]TCTATGCAAAAATCA | 9690 |
rs375367300 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205930 | AGCCAAGCTCCTTAC[A/G]GCCCCGCTAATTAGA | 9690 |
rs375395345 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261101 | TGAGGCCAGGAGTTC[A/G]AGACGAACCTGACCA | 9690 |
rs375397361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157247651 | GAGCTGAGATCGCGC[A/G]GCTGCACTCCAGCCT | 9690 |
rs375402281 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261340 | AAAAAAAAAAAAAAA[A/T]CCCAAATAGACTAAA | 9690 |
rs375408954 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160378 | TGCAGCAGCCACTTT[-/T]CAAATTTAACTTTAA | 9690 |
rs375440727 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204980 | CAAGATCTAGACAGA[A/G]GTTAGGGATTGCCTC | 9690 |
rs375483579 | in-del | AC/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227552 | AAATACAAAAAAAAA[AC/T]AGCTGGGCGTGGTGG | 9690 |
rs375484208 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250375 | TGTTTTTTGTAGAGA[G/T]AGTGTTGCCCTGTGT | 9690 |
rs375484622 | in-del | -/ATA | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157214256 | TTAACATTTAATTGT[-/ATA]ATAATTTAGTAGAAG | 9690 |
rs375495846 | snp | A/C/G | 0.000183833 | 0.00958565 | intron-variant | UBE3C | GRCh38.p7 | 7:157184080 | GCAGGCAGCCCCGTC[A/C/G]GATCTTCTAGCTTTC | 9690 |
rs375568698 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253619 | TGACTTAACGGTGAT[G/T]GTTTGCTTCATGTCT | 9690 |
rs375631649 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263663 | GCAAGACGCCAACTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs375663233 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138426 | TGCGTGTCATAGACA[C/T]AGAACAGGTGGGATG | 9690 |
rs375669997 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209962 | AAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTTG | 9690 |
rs375693521 | snp | A/C/G | 0.000115793 | 0.00760826 | intron-variant | UBE3C | GRCh38.p7 | 7:157184048 | AGCCCCGTGCCCTGC[A/C/G]TCTGGGGGGCTGCGA | 9690 |
rs375694393 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190021 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 9690 |
rs375728319 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226404 | CTAATATATTAGCAG[C/T]TTTAACTTCCAAATA | 9690 |
rs375794188 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160586 | AGTAGTTCATTATGC[C/T]GTTATGTTTTATTAC | 9690 |
rs375797018 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155462 | ATATTTACAAACATG[C/G]TAACAATCGTTCTGT | 9690 |
rs375803712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157152105 | AAGCTGTCCAACCAT[A/G]GAGACGTGGTGTTCA | 9690 |
rs375811001 | snp | A/G | 7.33501e-05 | 0.00605555 | intron-variant | UBE3C | GRCh38.p7 | 7:157253906 | TTTTTTTTTTAACCT[A/G]TTATCATACTTTGAG | 9690 |
rs375822965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141898 | TGTTTTCTTACAGAC[C/G]TTTGCTGTGTGTGCC | 9690 |
rs375831059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179731 | TCACCTGAAGTCATA[A/G]TCTGGGTTACATCTA | 9690 |
rs375850651 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183913 | CTGCTGGTGTATTTG[C/T]GGGTGCTGCAGACCT | 9690 |
rs375862036 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157260326 | AAACGCTGCCGCCTA[C/T]AAGCAACACACCTAA | 9690 |
rs375868628 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247413 | TAGAAAACTTTTGGC[C/T]GGGCAGGATGGCTCA | 9690 |
rs375892262 | snp | C/G | 1.67508e-05 | 0.00289398 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170342 | TGATCGCTGTGCTAC[C/G]TTGTCACAGTCCGGG | 9690 |
rs375894842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263509 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTAGGT | 9690 |
rs375941486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157221171 | TTCATTGGTTGAAAG[A/G]CATTTGGTTATTTTT | 9690 |
rs375964160 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167630 | GCAAGCTCCACCTCC[C/T]GGGTTCACGCCATTC | 9690 |
rs375977603 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247773 | ACATAGCCACCCTCA[C/T]TCATTGACACATTGT | 9690 |
rs375978981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157178952 | GTCTCAATGTCAGAG[C/T]GGTACTGGTGTCCCA | 9690 |
rs376001864 | snp | C/T | 0.000132159 | 0.00812787 | intron-variant | UBE3C | GRCh38.p7 | 7:157169032 | TTGCTCCCTCACTCC[C/T]CCTTTTATTGTTTAG | 9690 |
rs376006095 | in-del | -/TG/TGTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242515 | CTGAGCCTGAGTTGT[-/TG/TGTG]TTTTTTTTTTTTTTT | 9690 |
rs376020830 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175925 | GTTTGTGGTCCACAT[A/G]TGGTCTCTATTATGT | 9690 |
rs376039374 | snp | A/C/G | 0.00050376 | 0.0158639 | intron-variant | UBE3C | GRCh38.p7 | 7:157187032 | GTCAGGCAAGTGTCC[A/C/G]TGGGCGTCTGTGCCA | 9690 |
rs376135614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201118 | CACTTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 9690 |
rs376141565 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245578 | GCCATTTTATTCATT[A/C]TCTCATTAAGAAACC | 9690 |
rs376159672 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145204 | CTGGATTGTGCCAGC[A/G]CATTCCAGCCTGGGT | 9690 |
rs376171052 | snp | G/T | 1.6522e-05 | 0.00287414 | intron-variant | UBE3C | GRCh38.p7 | 7:157225393 | ATAACCTTACAGCTT[G/T]CCTTGTTTGTTAGAT | 9690 |
rs376177843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190496 | CATTTCAAGTGCCCA[A/G]TAGCCACATGTGGCC | 9690 |
rs376200046 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240742 | GGAGACCTGTGGAGT[C/T]GAGGTCCTTCAGGGA | 9690 |
rs376211250 | snp | G/T | 3.29728e-05 | 0.00406021 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178747 | TCCAATGAGAATGCT[G/T]GAAGTATTTTCGTCT | 9690 |
rs376227077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241640 | AGCCACTTTGGAAAA[A/G]TTTAGCAGTTCCTCA | 9690 |
rs376266739 | snp | A/G | 0.000512105 | 0.0159934 | intron-variant | UBE3C | GRCh38.p7 | 7:157248612 | AGGATTCACATACCT[A/G]TATAGCAAGTAGCAG | 9690 |
rs376297864 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241987 | GGTGGGTGAGTGATC[A/G]CCAGGGCTGGGAGGA | 9690 |
rs376302779 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224229 | AGATGGAGTGTCCTC[-/G]TGTCGCCCAGGCTGG | 9690 |
rs376330522 | in-del | -/TTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169231 | CTGACAGTAGTATTC[-/TTC]CCAATAAATAATTTT | 9690 |
rs376379880 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165242 | CCTCCTCTCCTACTT[A/G]GACGCAAACTGTAAA | 9690 |
rs376390733 | in-del | -/AA/AAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245992 | GGGAGACTCCGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 9690 |
rs376400198 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157159757 | TAATCCCGGCGGCGG[A/C]GGTTGCAGTGAGCCA | 9690 |
rs376423473 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204398 | AGGGAAACTTTGTTT[-/C]AAAAAAAAAAAAAAA | 9690 |
rs376423476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192356 | GCCATCTGCGGTGGA[A/G]CCGCCACCAAAATGC | 9690 |
rs376432547 | in-del | -/CA | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157211739 | AGAGTGTTTTATTCT[-/CA]GTTATTTGAACACTC | 9690 |
rs376505595 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157236398 | GCATGCCTATAAATC[A/T]GATTATTTGATATGA | 9690 |
rs376523188 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265405 | GGAAGGTGGAGTCAC[C/T]GGTTCTTCGTGGCCA | 9690 |
rs376542929 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206514 | TGATCCACCCACCTC[A/G]GCCTCCCAGAGTGCT | 9690 |
rs376556506 | snp | C/G | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182194 | TCATTCCGGCGCTTG[C/G]AGATGCGCAGACCGT | 9690 |
rs376580018 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209157 | AGGGCCCATTAATGC[C/T]TGCACTTAACCTGAT | 9690 |
rs376594298 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138248 | GGTTTATCAGGACAA[A/G]GCCCCATGGTAAGTC | 9690 |
rs376595266 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219472 | TTAAATCTAAATGTG[G/T]TGGAACCTCTACATC | 9690 |
rs376621173 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175835 | TAGTTTGAAAAACAC[A/G]TTGTATACATTCTTT | 9690 |
rs376672606 | in-del | -/AA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246013 | AAAAAAAAAAAAAAA[-/AA]CAGTGTTCTTCACAA | 9690 |
rs376722464 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211500 | TTTTTCAAAATACTC[C/T]AGTTTTTAACCCGTT | 9690 |
rs376722650 | snp | C/G/T | 9.8973e-05 | 0.00703404 | missense, synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181639 | TCTAAAACCATTGCA[C/G/T]TTTACTTACAACTCC | 9690 |
rs376725850 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBE3C | GRCh38.p7 | 7:157254345 | TATTGTTTCTGAAAA[C/T]GTTGCAGGTGGTCAT | 9690 |
rs376738509 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201731 | TTTAGGCTTCTCTAC[A/G]GTTTAGCCTTTAATG | 9690 |
rs376740080 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204572 | ACCACATTTAAACAA[A/T]CTCCAGATGGATAGT | 9690 |
rs376741044 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203193 | TTACTTCAAATTTTT[-/T]CATTTTTTTAATTGA | 9690 |
rs376744655 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137823 | CCCGCCTTGGCCTCC[C/T]AGAGTGCTGGGATTA | 9690 |
rs376777362 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157266297 | CCAGCCTGGGTGACA[C/G]AGCAAGACTCCGTCT | 9690 |
rs376798215 | snp | C/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191352 | GCTGGAGTGCCGTGG[C/G/T]GTGATCTCAGCTCAC | 9690 |
rs376811709 | snp | A/G | 8.2573e-05 | 0.00642493 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267703 | ACGAGACACTTTTGC[A/G]AAGTAAACTTCTCTA | 9690 |
rs376828090 | in-del | -/AAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266593 | GTTTAATGTGCTTCT[-/AAA]AAAACAGCCGTGTTC | 9690 |
rs376861022 | in-del | -/ATTAA | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269099 | TAATTTGAATAATAA[-/ATTAA]GCGTTTAAATGCTAT | 9690 |
rs376868017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194982 | TTGATTTGGGAAATT[C/T]GTGGCCTATTCAAGG | 9690 |
rs376941348 | snp | G/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225428 | CAGAGGTTGATTTAT[G/T]CAGATAAGCAAGAAG | 9690 |
rs376974804 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256940 | GCAGACCATCCTGTT[A/G]TTAAGGTCTTCTGGA | 9690 |
rs376979454 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160727 | ATCCTGTTTCTCCTC[A/G]AACTTTTGCCCACTA | 9690 |
rs377037654 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206022 | ACATCTCATCTAATA[A/T]ATACCTGTAGTTTTG | 9690 |
rs377042297 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184822 | AGCAATAAGAAAAGG[A/C]TCGATAAGTCAGCTC | 9690 |
rs377043365 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201294 | GTGGCACTGCACTCC[A/G]GCCTGGGCAACAGAG | 9690 |
rs377043435 | snp | C/T | 1.65323e-05 | 0.00287505 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157175023 | AAAAAGATTGATGAG[C/T]CTCTGTTGCAGGTAA | 9690 |
rs377046920 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223189 | AATCTTCACCTTAAG[A/G]ATTGTCAGTGGGAAT | 9690 |
rs377062249 | snp | A/G | 1.70729e-05 | 0.00292167 | intron-variant | UBE3C | GRCh38.p7 | 7:157170453 | CTCAAAACGTTTGGT[A/G]AGTGTTAACTACATT | 9690 |
rs377067062 | snp | G/T | 0.000133679 | 0.00817444 | intron-variant | UBE3C | GRCh38.p7 | 7:157248336 | AAGGCTTGTATATTC[G/T]ATGCTAACGTTGTCA | 9690 |
rs377089575 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157169563 | GTATTGTTAGTAGAG[C/T]CGGTGTTTTGCCACG | 9690 |
rs377122510 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243959 | GTATGTTGCCAGGCG[C/T]GGTGGCTCACACCTG | 9690 |
rs377188347 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157242853 | CGAGGTCAGGAGTTC[G/T]AGACCAGCCTGACCA | 9690 |
rs377263149 | in-del | -/TTTTGAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234187 | AACGAACATTTTTAA[-/TTTTGAA]GTCTAACGTGTTTTT | 9690 |
rs377294099 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240180 | GTGCCTCAGCCTCCC[A/G]AGTAACTGGGACTAC | 9690 |
rs377392736 | in-del | -/ACCACCTTCCCCGGGCACCTGTCCTAACGCCACCTTCCCAGGCACCTGTCGTAAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263225 | GCTTCGTGTCCTAAC[lengthTooLong]GCCACCTTCCCCGGG | 9690 |
rs377393340 | snp | A/C/G | 6.58939e-05 | 0.00573962 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183973 | AGCGCGAGCTGTCAC[A/C/G]ACTCAGCCAGTGACT | 9690 |
rs377415445 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236400 | TGCCTATAAATCAGA[-/T]TTATTTGATATGATC | 9690 |
rs377423498 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264419 | GTTACACACACACAC[A/C]CACACCTGGTACTAC | 9690 |
rs377435491 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248565 | TGTGGTGAACAATGA[C/G]CTGGGAGAGGCGCAG | 9690 |
rs377487775 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208933 | CTAGATTTACAGTCC[G/T]TTTAATACCAGCGAC | 9690 |
rs377523318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220283 | AAATAACTTGAGAAA[A/G]TATACTGTGTCTGTT | 9690 |
rs377535996 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157244726 | CGACTGCACTCACTT[A/C]TATTAAAAGGCTTCT | 9690 |
rs377548530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165457 | GGCTGGACTGCAGTG[G/T]CACGATCTCAGCTCA | 9690 |
rs377554868 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229416 | ACCTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 9690 |
rs377574170 | in-del | -/CGTTA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156575 | CTCCAAAACTGCTAG[-/CGTTA]CGTTACAGGCATGAG | 9690 |
rs377597875 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251193 | CAAGTTTTTAAGTTT[A/G]TAAAGTATGATTTAA | 9690 |
rs377650153 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215123 | CGAAATACCCACCAC[A/T]TATAAAGGTGCATCT | 9690 |
rs377667592 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE3C | GRCh38.p7 | 7:157223372 | CAATTTGGCTTCTTT[A/G]TTGTCACTACGTATC | 9690 |
rs377669754 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157197440 | TAATCCAGATTTGTC[C/T]ATATTCAGGTTGGAA | 9690 |
rs377682676 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179687 | AGAGCCGTGGCTGCA[A/G]ACAGAATTATAAGCA | 9690 |
rs377688008 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144365 | GGAAGATTGGATGAT[A/G]GAGGGAAATTCGGTG | 9690 |
rs377697494 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231848 | CAGTCAAAACGGACT[A/G]AGACAGTAAGTTACT | 9690 |
rs377717409 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241581 | TGGTGAGGATGTGGA[A/G]GAATCAGTCCTCATG | 9690 |
rs377719804 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232391 | CGGAGTCTCTCCTTG[C/G]TCTGTTGCCCAGGCT | 9690 |
rs377732252 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252397 | GAATTAAGATAATGA[A/G]CACAATCTTTAATCA | 9690 |
rs377733726 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267979 | TTAAAATAACACGTT[A/G]TGTGCCATGTGGCTA | 9690 |
rs386411800 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262435 | TTTTTTTTTTTTTTT[-/TT]TGAGATAGAGTTTCG | 9690 |
rs386720126 | in-del | AT/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156092 | TTCTCCTGGTACCTT[AT/C]TTGCCCCTTTCCTCC | 9690 |
rs386720128 | in-del | AATATT/TA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189388 | TTTAAAATATGATTA[AATATT/TA]CACTGGCTATATTTT | 9690 |
rs386720129 | in-del | AGA/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157199382 | TTTTAAATATCTCAG[AGA/G]TAGGGTATCTATTAT | 9690 |
rs386720130 | in-del | CA/GCGTGTGAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200014 | CCCCACTTTGTCATG[CA/GCGTGTGAC]TGATAAACATCATGC | 9690 |
rs386720131 | multinucleotide-polymorphism | AG/TC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216119 | ATTTTTCTGGAGTTA[AG/TC]ATCACAGATCTGACT | 9690 |
rs386720132 | multinucleotide-polymorphism | ATCAGA/GTCAGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236181 | TTTTGTCGCCTGTAA[ATCAGA/GTCAGG]CTGCAGACAGGGAAT | 9690 |
rs386720133 | multinucleotide-polymorphism | ACATTACAGGCGTGAGCCAGCG/GCATTACAGGCGTGAGCCAGCA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237001 | CCTTCCAAAGTGCTG[lengthTooLong]CACCCGGCAAGACAG | 9690 |
rs397696077 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157172039 | ATCTTTTTTTTTTTT[-/T]CCTTTTTGAGACGGA | 9690 |
rs397723527 | in-del | -/T | 0.375 | 0.216506 | intron-variant | UBE3C | GRCh38.p7 | 7:157223578 | AAGAAATCTATAGTG[-/T]TTACTGGCTTTCAAT | 9690 |
rs397767294 | in-del | -/CTTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234130 | GCAAGTATTTTCTTC[-/CTTC]TCTGGATTGTCTCTT | 9690 |
rs397836107 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169388 | ttttttttttttttt[-/TT]aaattgagactgagt | 9690 |
rs397952578 | in-del | -/GTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166944 | GTGGTGGTGGTGGTT[-/GTT]TTTGAGACAAAGTCT | 9690 |
rs397962732 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154003 | CCTGTCTGGGGGGGG[-/G]AAAAGTTAACTTTTT | 9690 |
rs397972109 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216365 | GGTTTTTTTTTTTTT[-/T]AATATTTTAGGTTTG | 9690 |
rs397972242 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187392 | GGGGTTTTTTTTTTT[-/TT]CTTCTTCTTCTTCAG | 9690 |
rs397974548 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171125 | TTTAGGGTCTCTTTT[-/T]GTGGGGAGGGCACTG | 9690 |
rs398039299 | in-del | -/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157196756 | GTCTCAAACTCCCGA[-/C]CCTCAGGTGATCCAC | 9690 |
rs398039300 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157186429 | AGAGTATTACATAAA[-/T]TTTTTTTTTTTTTTG | 9690 |
rs398039301 | in-del | -/A | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157148114 | GGGAGACTCTGTCTC[-/A]AAAAAAACAAAATAA | 9690 |
rs398048211 | in-del | -/A | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157147073 | TATTCACAAAAAAAA[-/A]CCTGTGGAATTTTGA | 9690 |
rs398048212 | in-del | -/A | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157159336 | ATTAAAAAAAAAAAA[-/A]CAGAATTAGGATTAA | 9690 |
rs398048213 | in-del | -/TTT | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157175139 | GGCTTTTCCATACTT[-/TTT]TTTTTTTTTTTTTTT | 9690 |
rs398048214 | in-del | -/GTC/GTT | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157242516 | TGAGCCTGAGTTGTT[-/GTC/GTT]TTTTTTTTTTTTTTT | 9690 |
rs398048215 | in-del | -/AC | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264407 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs398095510 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246231 | CGCATTTTATAGACT[-/T]ACACATACGAAGTAG | 9690 |
rs527242166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168343 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAGGTCCTA | 9690 |
rs527254791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157162482 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTAAAT | 9690 |
rs527256776 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231827 | TTTCAGGTCTTCTGT[C/T]ATAAGCAGTCAAAAC | 9690 |
rs527288270 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161348 | ATGAATCATTTTAAT[A/T]AAGTTTAAAACAATA | 9690 |
rs527303777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212848 | CTGCAACCTCCACCC[C/G]CCAGGCTCAAGTGAT | 9690 |
rs527314098 | in-del | -/ATT | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157242352 | ATCATCGAAGGCATC[-/ATT]GTCCTCAAATTTCTC | 9690 |
rs527335222 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230165 | TCCGCCCACCTCAGC[A/G]TCCCAAAGTGCTGGG | 9690 |
rs527338491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211993 | CGGTTGTTTTCCAAC[A/G]AGGTCATGTTCTTAG | 9690 |
rs527349177 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246551 | GGTATTCCCTGGGTA[A/G]CACCATAGCACTTGA | 9690 |
rs527389498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245946 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACACTC | 9690 |
rs527391669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167952 | GAACATTTTAAAGAT[A/G]CTCTCAAGTCAATGA | 9690 |
rs527428445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173899 | AGTAGTTCAGAATTA[C/T]TTCATCCCAGTTTAA | 9690 |
rs527440631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157181883 | GGTTATTTTCCTGCT[C/T]TTCTAAGTAACTGTC | 9690 |
rs527451594 | snp | A/G | 0.000265692 | 0.0115228 | intron-variant | UBE3C | GRCh38.p7 | 7:157186798 | ACGTTCCAGTTGAGC[A/G]CATTTATGGAGACTG | 9690 |
rs527451932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157193350 | ACAGATCATTGGGTG[C/T]CTCGCTGTTTCTTTT | 9690 |
rs527468011 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268755 | AAGACGGGACAGTCC[A/C]TGGTGCACATCCAGG | 9690 |
rs527482172 | in-del | -/T | 0.291235 | 0.246576 | intron-variant | UBE3C | GRCh38.p7 | 7:157216352 | TTCCAGATTCGTGGG[-/T]TTTTTTTTTTTTTAA | 9690 |
rs527502295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192717 | ATGAGCTGCCTTCGT[C/T]GAGAGTGCCCTTCTG | 9690 |
rs527503427 | snp | A/G | 0.149999 | 0.229128 | intron-variant | UBE3C | GRCh38.p7 | 7:157263264 | TAACGCCACCTTCCC[A/G]GGCACCTGTCGTAAC | 9690 |
rs527506565 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269267 | GACTGAAGAGAAATT[A/G]ACAATTCACTTATTT | 9690 |
rs527542527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151026 | GCTGGCCTCCCGCTA[A/G]GCTGCTGAGCAGACA | 9690 |
rs527571692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240982 | GGCAGTGACTGAACC[C/T]GGGAGAGGTAATGGA | 9690 |
rs527604693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163115 | AGATGGCCGGGCGCG[A/G]TGGTTCACGCCTGTA | 9690 |
rs527632133 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162376 | ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 9690 |
rs527634969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199400 | TAGGGTATCTATTAT[C/T]ATTTTCTAATACAGC | 9690 |
rs527640343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175291 | CCTTTGAATTATCTT[A/G]TGAATGATGGCCATC | 9690 |
rs527678726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144750 | ATCAAGCAGAGGGTA[A/G]GGTTCCCATATGCCT | 9690 |
rs527681533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258578 | AATTCTCCTGCCTCA[G/T]CCTCCTGAATAGCTG | 9690 |
rs527715392 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142970 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9690 |
rs527719495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252603 | GCAAACGAGTCTCCT[A/G]TAACCATCAGCTGTA | 9690 |
rs527739091 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139214 | CCAGCCCGCCCCGTG[C/G]CCCGCCCGCCCGGCT | 9690 |
rs527746213 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157263686 | AAAAAAAAAGTCTAG[C/G]AAGTATTAGGAACAT | 9690 |
rs527787299 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248903 | GTTCAGCAGCTTCCC[A/G]GCAGGACCCCTTGCT | 9690 |
rs527793045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157225075 | GCCTGAGTGCAGTGG[C/T]GCCTGCAACCTCTGC | 9690 |
rs527796795 | snp | G/T | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231216 | TAACCCCAACCAGGG[G/T]TTCTTTAAGACTACT | 9690 |
rs527862059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201012 | TGAGTCCGTCACTAA[A/G]TATTTTACAAATTTT | 9690 |
rs527868819 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202448 | GATCACCTGAGGTCA[A/G]GAGTTCAAAACCAGC | 9690 |
rs527928825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164655 | ATGACCTGCTTTTTT[A/G]GGTAGAGTTTTTTGT | 9690 |
rs527949139 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157214357 | CTTATGAACAGAGAT[A/T]GAATAGAAATAGATA | 9690 |
rs527959203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157247017 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTATA | 9690 |
rs527967298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164101 | GTTGACTTACATAAT[A/G]ATATGGTTTCCAGAA | 9690 |
rs527993131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157169362 | AAAATAGAAGGAAGT[C/T]ATGAGAGATCCTTTT | 9690 |
rs528060716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177577 | CCAGCGGCTTGTTAT[G/T]TGTAGCCCCGCTCCT | 9690 |
rs528067466 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157136959 | TTGAGACGGAGTCTC[C/G]CTCTGTTCCCCAGGC | 9690 |
rs528071097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223045 | ACATCTTTAATATTC[A/G]ATCAAGTTATGTGTT | 9690 |
rs528075291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216799 | TCCTCCTCGAGTGAA[C/T]GTATGGCTCACTGTG | 9690 |
rs528078281 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157260473 | CGCAGGGAAAGCTGG[G/T]TGCTGCCTGTGTGGT | 9690 |
rs528081885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183713 | CTTTCTGACATGAAC[A/G]GGGACAAAATCTAAA | 9690 |
rs528100951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260912 | AGCCTTCTCCACCTC[C/T]GTGATGCCTCCGGGT | 9690 |
rs528118096 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154278 | TGAGCCAAGATCACA[C/T]CACTGCACTCCAGCC | 9690 |
rs528122068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255306 | ACCCACTAGCTGTCT[A/C]CTGGTGCAAGTGAGA | 9690 |
rs528127730 | in-del | -/T | 0.423881 | 0.179625 | intron-variant | UBE3C | GRCh38.p7 | 7:157148732 | AGATCAAATTAGTTC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs528135579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141925 | TGCCTTTTGGTGCAC[A/G]TAATACTCTTGTGCT | 9690 |
rs528165336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147881 | TCTTGCGTATCTGGA[A/G]TAAATCCCACTTGAC | 9690 |
rs528203862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147264 | TTGTTAGATTTATAC[C/T]TAAGCGTTTATTTTT | 9690 |
rs528217029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157190166 | GGCTTCAGCTACATT[C/G]TAGTGACTCTCACAT | 9690 |
rs528255228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203387 | CCAAAATACAAGATT[C/T]TAAGTATGTTTTGTT | 9690 |
rs528259910 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224960 | TTTCCTCACTACCTA[A/C]GTTTTTATAAAGGAT | 9690 |
rs528291555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210419 | CTGCTGTTAGCTGTT[C/G]TTTTAAGAAAATACT | 9690 |
rs528335932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217300 | TATTTAAAAGAGATA[A/G]ATCTTATACCTAATT | 9690 |
rs528337941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262456 | TAGAGTTTCGCTCCT[A/G]TTGCCCAGGCTGGAG | 9690 |
rs528343775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157241540 | ACCCGCGAGTACGGC[A/G]GGAATCAAACCAGGA | 9690 |
rs528360348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248879 | CTCTTCCCGGTGCTG[C/G]GGGTGGCCGTTCAGC | 9690 |
rs528362274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157255922 | TAAAATTAATTTAGC[C/T]ACCAAATCATGCTGG | 9690 |
rs528393042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157166509 | ACTTTGGGAGGCCGA[A/G]GCAGGCCGATCACCT | 9690 |
rs528445327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191247 | TTCTTTTCTGTGCAC[A/G]CGCGTGTGTATGTGT | 9690 |
rs528483898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157197757 | AAGTTCCGGACATCC[A/G]GGATCCTGTGTGTAC | 9690 |
rs528518958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267446 | AAACAACAACAACAA[A/T]GCAAATGTGGTTTCG | 9690 |
rs528525696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155419 | AAACAAAAACCTCAC[A/G]GTTTTTTGGGGTTTT | 9690 |
rs528548613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234567 | TATCCTGGATATAGA[A/G]TAATTCCCCTTTATT | 9690 |
rs528565857 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157239705 | AAGATGGGAGAAATA[A/T]CAGCATGTGTATTTG | 9690 |
rs528570401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154500 | CTTTTTCACCTCAAC[A/G]AAATATCTTAGTGAT | 9690 |
rs528621323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157160842 | TCTGTGAGGAAAAGA[A/G]TTTTCTTTTCCTTGT | 9690 |
rs528653573 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267213 | CAGATCACAAAGTCA[A/G]GAGTTCAAGACCATC | 9690 |
rs528686664 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162858 | AAATTTACAAAAATA[A/C]AATGTCCATACACTA | 9690 |
rs528694786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143681 | TTCAGATGGAACAGT[C/T]TAGGTGCACCTGAGG | 9690 |
rs528713274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143110 | GACCTCAGGTGATCC[A/G]CCTGCCTCAGCCTCC | 9690 |
rs528718337 | in-del | -/AC/ACAC | 0.0325576 | 0.123365 | intron-variant | UBE3C | GRCh38.p7 | 7:157264518 | TGCTCGGCCTGTTAC[-/AC/ACAC]ACACACACACACACA | 9690 |
rs528733546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229908 | GTGAGCCTCTGTGCA[A/G]TGTTTTAATTTATTT | 9690 |
rs528742573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261708 | AGTTATGAAACTCCT[A/T]AGTGCCAGATTATTG | 9690 |
rs528752650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223789 | GTTGGGCGTGGTGGC[A/C]TGTACCTGTAGTCCC | 9690 |
rs528804380 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232955 | TCAGTGGTTTTTAAT[A/C/G]TATTCACTGTGTTAT | 9690 |
rs528860788 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157242327 | GTACCTGATGGTAAC[A/G]AAATCTGTTATCATC | 9690 |
rs528879639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210542 | AATAGTTCTGTGAGA[A/G]AGATACTATAATTTG | 9690 |
rs528916056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249499 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCTCCAT | 9690 |
rs528917750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260994 | AGTAGAGGGATTTAC[A/G]TGAGCTTTTAAAATC | 9690 |
rs528939743 | snp | A/G | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182301 | TGGCTTTTCTATTTC[A/G]TTTTAACTGTTGGCG | 9690 |
rs528968211 | snp | A/G | 4.66211e-05 | 0.00482788 | intron-variant | UBE3C | GRCh38.p7 | 7:157223166 | GAGTTAATCAGGATG[A/G]TTTCAAGAATCTTCA | 9690 |
rs529002137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222625 | GAGGCAAGGTCTCTC[C/T]GTGATGCTCAGTTTC | 9690 |
rs529002228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157228745 | TGTCCATTCAGTCAG[C/T]GACCACTGCTCAGTG | 9690 |
rs529008923 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157184227 | TTAGCACGTTCATGG[A/G]AGTGTAAATGGAGAC | 9690 |
rs529056394 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203792 | ACAGTGTATTAATGC[A/G]TTCCCAATACAGATA | 9690 |
rs529076034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204279 | AGGCTTGCATTGCTA[A/G]GACTTACAGCTTTAG | 9690 |
rs529114167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203513 | ATTAGGACAGGAAAT[C/T]ATCGTTTACCCATAA | 9690 |
rs529145083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157250075 | ATAAGGGATACTGAC[C/T]CTGTGTGGTGAGAAC | 9690 |
rs529155505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167493 | GGAAGTGATGCTCAC[C/T]TGTAAGATGACTGTG | 9690 |
rs529167666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173142 | ACTTTGTGGGGCTGA[C/G]GTGGGAGGATCCCTT | 9690 |
rs529174075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244228 | GATAGAGTGAAACTC[C/T]GTCTCGAAAAAAAAG | 9690 |
rs529204605 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219364 | CACACACCCACACTT[G/T]AAGTAGGTTTCACTT | 9690 |
rs529249112 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151799 | AGTCAGTCAGCCCTT[A/G]GTTTGTCACCATGAC | 9690 |
rs529261018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143764 | GTTCCTGTGGGACAG[A/G]CACAGGAAGGAGTCT | 9690 |
rs529271331 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163017 | TATGAAAAAAAATTT[G/T]CATCAAAGAAATTGA | 9690 |
rs529289705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185251 | GAAAGCAGAACATGC[A/G]GACCCGTGAACCGGG | 9690 |
rs529306954 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185758 | ATTGTACACTACAAA[A/T]ATAGTAGTGCTAGGA | 9690 |
rs529325422 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157262493 | GGCCCATCTCAGCTC[A/G]CTGCAACCTCTGCCT | 9690 |
rs529337487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157143220 | AATATTTCTGACATC[A/G]GGATACACACTGATA | 9690 |
rs529396466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198390 | TGTCATCCCTTTGGC[G/T]GTTTTCAAGTTTCTT | 9690 |
rs529405352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235103 | GGCTGAGGCAGGATA[A/C]TGGCTTGAACCTGGA | 9690 |
rs529407547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155438 | TTTTGGGGTTTTTTT[A/T]AAATCAAGATATTTA | 9690 |
rs529413721 | in-del | -/CT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183786 | TCTGGTCAGAAATGC[-/CT]CTCTGCGTGTGAGGA | 9690 |
rs529445918 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157164663 | CTTTTTTAGGTAGAG[-/T]TTTTTGTTTTGTTAT | 9690 |
rs529454889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212897 | TGAGTAGCTGGGACT[A/C]CAGGCATGTGCCACC | 9690 |
rs529459497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174511 | CAGTGCAGTGGCTTG[A/T]TGTTGGCTCACTGCA | 9690 |
rs529464343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257644 | TGGGAGGCTGAGGCA[C/T]GAGAATTGCTTGAAC | 9690 |
rs529498872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251832 | TTAAAAGTAGTGTAA[C/G]CGTTTAAAAGTTATT | 9690 |
rs529501220 | in-del | -/AAAC | 0.00380082 | 0.0434277 | intron-variant | UBE3C | GRCh38.p7 | 7:157153824 | TATACTAAAAATACA[-/AAAC]AAACAAACAAACAAA | 9690 |
rs529502342 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139008 | TGCTGCCCGCTGGGC[C/G]CCCCTGCAGCGGCCC | 9690 |
rs529511524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157218444 | ACAGAGCAAGATTCC[A/G]TCTCAAAAAATAAAA | 9690 |
rs529517241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212307 | GTTATGATGCAATTT[A/G]GTCTTTCAGTTGCCC | 9690 |
rs529535753 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138567 | CCCCGCACCCTGCCC[C/T]GCACCCCATCCCGGC | 9690 |
rs529546705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224341 | CTAGGACTACAGGCA[C/T]GTGCCACCATGCCTG | 9690 |
rs529568704 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157263204 | TCTGCCCACCGTAGC[A/C/T]GCTATGCTTCGTGTC | 9690 |
rs529591803 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155266 | CTTTACTCAAAGGCA[A/G]TGTTCTTTGAAGTGT | 9690 |
rs529599518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173950 | GCAGAGTGCTTTTGT[A/G]TTGGTAATTTCATTG | 9690 |
rs529601496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180106 | TGCTTAAAAATCTTA[C/G]ACAGAAACTGCCGCT | 9690 |
rs529641720 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157179546 | CAGTATAAATCCTAA[C/T]ACAAAAGAACCTTTG | 9690 |
rs529660703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188467 | TAGCTCTTTGCCGGC[C/T]AATTGCATGAGAGCA | 9690 |
rs529661268 | in-del | -/GAGTGTTTCAGAACAATTT | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157218502 | GAGGAGAGAAAACAG[-/GAGTGTTTCAGAACAATTT]TATAAGCATGACTAT | 9690 |
rs529685881 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232507 | GGTGTGCACCACCAC[C/G]CCCAGCTAATTTTTC | 9690 |
rs529690260 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173838 | CAAGGTGGCTCCAAA[C/T]ACCTCAAGAGAAAGC | 9690 |
rs529702391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157195131 | CAAGTCACACAAAAG[A/G]CTCTTTGAGGAGATT | 9690 |
rs529706674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141650 | TATGTGGTCTGTTGT[C/T]GACAGACTGAGAGGT | 9690 |
rs529722717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157231894 | GTTTAATAGGACTGC[C/T]GCAACAAATTACCAC | 9690 |
rs529729616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193580 | AGTAATTTTTAATCT[A/G]TCCCACTATGTGGGA | 9690 |
rs529739564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157152246 | AGAGCTGGGGGAAAG[A/G]TAATTAGGGACAGAG | 9690 |
rs529742664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152713 | TGTTTATCCGGATGC[C/T]GTACGGCCTCTCCCT | 9690 |
rs529770972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237583 | AGCAATAGTTAAACA[A/T]CTGAAATTCATGAGA | 9690 |
rs529774869 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191932 | AGTGATATTTTCATT[A/G]TAATCAATAGAATTA | 9690 |
rs529804036 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198516 | CCCTCCGCCATCTTC[C/T]GCTGGCTGTATTTGT | 9690 |
rs529838601 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216425 | TAAACATGTCATCGG[A/T]GTTTGTTGTACGCAT | 9690 |
rs529854574 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157241240 | GAAAAAATCCCGTCT[G/T]AGCTGTGAGACCAGG | 9690 |
rs529867283 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151241 | GCTGCAAAACAAATA[C/T]GCTGTGTTTTCTGCC | 9690 |
rs529871626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176953 | TGCCAGAACATTGAA[C/T]TTTTCTTTTTCTGTA | 9690 |
rs529876986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141410 | ACTAGTCCAGTTGGT[G/T]GTTGTGGGACCGTCC | 9690 |
rs529897704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216076 | CAGGCCAGCCTGTTT[A/G]GAAAGGTTATCAAGG | 9690 |
rs529909688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157227447 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 9690 |
rs529948134 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148982 | CTGCATTTGTTCCTT[C/T]GAATACAGTTATGCT | 9690 |
rs529960963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176255 | CAGCAGAGCAAGACC[A/G]TGTTTCTTTTTTTAT | 9690 |
rs529997713 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221283 | GAGTAAGTTTCACTG[A/G]GAGTAAGAATCCTGA | 9690 |
rs530028094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157195872 | GGGTGGAGTGGTGGC[A/G]GGGCGGGGGTTGCAC | 9690 |
rs530044157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182696 | ACATACATACATACA[C/T]GCATGAATTATTCAT | 9690 |
rs530048817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263544 | TGATGGGCACATATA[C/G]TCCCAGCTACTCGGG | 9690 |
rs530065729 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157209655 | AATATCAGGTGTTGT[G/T]TATGATATCAGATAA | 9690 |
rs530075273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157159522 | TAAAGCAAAATGGCA[C/T]TTTGGTTAGGAATTC | 9690 |
rs530079241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243610 | TGCTGCTGTTCCTGC[A/C]TGTGAGGCGCAGGGG | 9690 |
rs530083443 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219100 | GTTGCAGGCTCTGGT[A/G]AAGGAGATGACCAGG | 9690 |
rs530087808 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239472 | CAGGGGGCTTCCAAG[C/G]TGCTAGGCATTTTCT | 9690 |
rs530131569 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252117 | CTCCAGTGTGGGTGA[C/T]AGAGTGAGACCTTGT | 9690 |
rs530135215 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228606 | GAAGCAGGAAAGCAA[G/T]CTGGAGCCAAATGGC | 9690 |
rs530141373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243277 | TTTATGGAGTGCCAG[G/T]GTCTCAAGGAAGAAA | 9690 |
rs530186421 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161722 | GCCTTCCAAAGTGCT[C/T]GGATTATAGCCATGA | 9690 |
rs530197091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183790 | GTCAGAAATGCCTCT[C/T]TGCGTGTGAGGAAAA | 9690 |
rs530219764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148630 | GGTGTAATGGATGTG[A/T]TAGTATAATGCTCCA | 9690 |
rs530228486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157171375 | TCAAGTGATCCTCCC[A/G]CCTCATCCTCCCAAA | 9690 |
rs530250696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266934 | TTTAGTGGAAATGAG[G/T]TCTCGTTATGTTGCC | 9690 |
rs530265183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200812 | ATAGAGATGAGGTCT[C/T]ACCACATTGCCCAGG | 9690 |
rs530293677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153984 | CTTGGGTGACAGAGC[G/T]AGGCCCTGTCTGGGG | 9690 |
rs530302366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142030 | CATCTGAAGGTATCC[A/G]GGTTTCCACATCCTT | 9690 |
rs530309318 | in-del | -/A | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137331 | CAACCTCCGCCTCGC[-/A]GACACAAGCGAGTCT | 9690 |
rs530330939 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157160064 | TTTATGTAATTCCGT[A/T]GTTACTTTTTTTTTT | 9690 |
rs530342254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147935 | CGATGTTAGATTGAG[C/T]TTGTTGATATTTTGT | 9690 |
rs530351107 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198497 | ACCGAGCTCAGGGCC[A/G]CCGCCCTCCGCCATC | 9690 |
rs530355420 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178587 | TTCAGAGATAATCTT[A/G]TACTGGAATAGTTTC | 9690 |
rs530360329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228153 | ATGCTCGTTGTCTTA[C/T]CTCCGAACGATTCTC | 9690 |
rs530400727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233847 | TCAGTGACTCCACAT[C/T]GTTGTCAGCACTTAC | 9690 |
rs530436892 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157182761 | TTGGGGGTTGGGTGC[C/G]GGGGGGTATATAGAG | 9690 |
rs530459620 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263768 | TTTTTTTTTTTTTTT[-/TT]ACCTTTCAGTAAAAG | 9690 |
rs530472015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196345 | CTTGTTATGGTGGCA[A/G]TGGGAAACTAACCAG | 9690 |
rs530510385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141465 | TAGCCAGTGTTGCCC[A/C]CTGCACACCTAGCTG | 9690 |
rs530535103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232585 | TTTAACTCCTGACCT[C/T]AAGTGGTCCACCTGC | 9690 |
rs530554220 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176618 | ACACTCCTCCTCATC[C/T]TTCCTCTTTAATCTC | 9690 |
rs530557722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157195624 | CATGGGAGCAGATAA[C/T]TTGTTTTCTAGGTTC | 9690 |
rs530566979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227481 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 9690 |
rs530569581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189054 | AGTATGTAGAAGAAC[C/T]GGCTTTTCCTATAAG | 9690 |
rs530587142 | in-del | -/AGGAAGGTAGTCAGGGACAGAGCTGGGA | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157152186 | GAAGAGAAGGCTGGG[-/AGGAAGGTAGTCAGGGACAGAGCTGGGA]GGAAGGTAGTCAGGG | 9690 |
rs530596649 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157265455 | ATAGGTCTCATGCAT[G/T]AAGTCTGCGTTGAGC | 9690 |
rs530619064 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157240321 | CAGCCTCCCAAAGTG[C/G]TGGGATTATGGGTGT | 9690 |
rs530624624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152753 | GCAGGTTGTCTTGCC[C/G]GCACATCTTGCTTCT | 9690 |
rs530647971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209264 | ACACATTTCTCTTAG[A/G]AGCATGAGCATTAGC | 9690 |
rs530648602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216749 | GCGGGTTTGGTGTCC[A/G]GCTCGACCTGGGTTC | 9690 |
rs530677392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172072 | CTTGCTCACTCTGTC[A/G]CCCAGGCTGGAGTGT | 9690 |
rs530681297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157254791 | CACGCCTGTAATCCC[A/G]GCCTTTGGGAGGCCG | 9690 |
rs530699534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239719 | AACAGCATGTGTATT[G/T]GCTGCTGGAAATAAG | 9690 |
rs530707082 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262282 | ATAAACTATAATTAG[-/A]AAAAAAAAGACAATG | 9690 |
rs530715228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221699 | GTGAACCAAGATCAC[A/G]CCACTGCACTCCAGC | 9690 |
rs530716811 | snp | C/T | 8.2991e-05 | 0.00644117 | intron-variant | UBE3C | GRCh38.p7 | 7:157248349 | TCGATGCTAACGTTG[C/T]CACTGTTCTCTTTTG | 9690 |
rs530762069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233898 | ACAGCCATTCTAGTG[G/T]GTGGGAATTGGTATC | 9690 |
rs530769074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157248837 | CTCCACTCTCGAGGC[C/T]GCGGCCCAGGCTTGC | 9690 |
rs530769559 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260516 | AGGGCTTGCTGTGCT[A/G]GGGACTAAAGAGCAG | 9690 |
rs530783665 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258829 | GAAACTATTTTAAAT[A/G]TATAGAAAAGTTGTG | 9690 |
rs530824073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203144 | GACAAAACAGTTCAT[A/G]CTAATGAAAGGGGAA | 9690 |
rs530862789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157177016 | TTTATGACTAATCAC[A/G]TACATATTTTTTAAT | 9690 |
rs530878296 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241187 | AGCGCTGCAGGGCAT[A/G]TGGGAAAATGGACTG | 9690 |
rs530912994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190328 | AAGAGCCTCCTCTTT[C/G]TGTCCCTGTTTTGGT | 9690 |
rs530920834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244122 | GTAATCCCAGCTGCT[C/T]GCGAGGCTGAGGCAG | 9690 |
rs530923519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239286 | GACTACAGCTACTCA[A/G]AATGGTATGAGTGAA | 9690 |
rs530985844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202675 | AAAAGAAAAAAAGAA[C/G]TCTATGCCAATCCCC | 9690 |
rs531002312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261062 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGT | 9690 |
rs531008137 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159155 | TCTCCTTGACTGTTA[C/T]CTCAAGAAGAGTGTC | 9690 |
rs531013401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160268 | TTAGTAGAGACGGGG[C/T]TCCACCATGTAGGTC | 9690 |
rs531035307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256048 | CGGCTTTGAACTGCA[A/G]CACGGTTCTTCAAAA | 9690 |
rs531039211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157149436 | TTGTCTCATTGTCTC[A/G]TTTTCTTTGGACATT | 9690 |
rs531043255 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183397 | GCGGGAATGGGGAGC[C/T]TCCATGCCTTCTCCA | 9690 |
rs531053008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157229505 | TGTATTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 9690 |
rs531105464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178116 | GGAGTGGCAGATGTG[C/T]TCTGTGTCTTGATTG | 9690 |
rs531115448 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137234 | TGAGCCACCGCGCCC[C/G]GCCTGTTTATTTTTA | 9690 |
rs531116841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154425 | GTATCCTCTCAGAAC[A/G]AGTCTAAACATAAAC | 9690 |
rs531116848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148061 | TGGAATGAGGATACT[C/T]TAGGGCCTACCAAAA | 9690 |
rs531124448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234497 | GGATTTATTAATAGC[A/G]GATGGGAGTAGAACC | 9690 |
rs531130051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202974 | ACACACTCATCTGCA[A/G]TCTAACTTGCTGTGT | 9690 |
rs531168329 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156509 | ACAGGGTTTCACTAC[A/G]TTGGCTGGGCTGGTC | 9690 |
rs531253209 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209897 | TTTAAGAGTTAGGGC[A/C]AGGCCGGGTGTGGTG | 9690 |
rs531261057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205867 | TGATGATGGCAGTGC[C/T]CTCCCCTGAACCATG | 9690 |
rs531288943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236424 | TATGATCTTGGTTAT[A/G]TATTTGAAAATTTCA | 9690 |
rs531289375 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232659 | ACCTGGCCTGTTATT[C/T]GCATTCTTAAATAAA | 9690 |
rs531310797 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187618 | AGTCTTGCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 9690 |
rs531341585 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209290 | TTAGCAGCAGCAGCC[A/G]TAACTGATAATGTTT | 9690 |
rs531399340 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157192588 | GTGTTGAGACTTCGT[-/G]GTGGTGCTAAGAAAA | 9690 |
rs531415039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162156 | TGGCTTAACTACTCT[C/G]TGACACTGTTCTGAT | 9690 |
rs531433838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144769 | TCCCATATGCCTAGT[C/G]TCCCTCACCTCACTT | 9690 |
rs531434967 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191533 | TGGGCCCAAGTAATC[C/T]GCTTGTCTCAGCCCT | 9690 |
rs531437839 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167850 | CTAAAGTGCCTCTCA[C/T]AGGGCTGGCACATAG | 9690 |
rs531485123 | snp | A/T | 3.30175e-05 | 0.00406296 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231261 | GTACCCCAACCCGGC[A/T]GCTCAGATGCTTGTG | 9690 |
rs531497242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157248805 | CCTGTTCCTGCCCGG[C/T]AGCCCCTCCTGCGGA | 9690 |
rs531522786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145378 | CAAAAATTAGCCAGG[C/T]GTGGTGACAGGTGCC | 9690 |
rs531550448 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | UBE3C | GRCh38.p7 | 7:157170135 | TTTTTTTTTTTTTTT[C/T]TTTTTAACCATTTTT | 9690 |
rs531553237 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269279 | ATTGACAATTCACTT[A/G]TTTGTGGTTTTTTTC | 9690 |
rs531565551 | in-del | -/T | 0.43598 | 0.167067 | intron-variant | UBE3C | GRCh38.p7 | 7:157201638 | TCTTCAGTGTATCGC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs531574595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231698 | CCCTGTGCCGCCTCC[A/G]GACTCTGCAGAGTCC | 9690 |
rs531578932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225594 | GGCTAGGGAATTGTT[C/T]TAGAAAATGGTGGTT | 9690 |
rs531634266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214540 | ATGACCTTTGTTAAC[A/G]GTTGGGGTGATTATG | 9690 |
rs531638054 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157166732 | AGTGAAACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 9690 |
rs531682680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175889 | TTTTTATGTAAATGG[C/T]GAGATAGCAAATATT | 9690 |
rs531688117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193379 | TTACCTGTGGCACCT[A/G]GACTTAGAGGGGAAT | 9690 |
rs531718337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175309 | AATGATGGCCATCCT[A/G]GTTACTGGAGAATGG | 9690 |
rs531729297 | in-del | -/TCTT | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157249319 | TTCACATCGATAGAG[-/TCTT]TTTTTTTTTTGAGAT | 9690 |
rs531769420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157218599 | CACTGACAAGGTAGA[A/G]CAATGGTGGCAGATC | 9690 |
rs531800331 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201786 | TTCTAATATCTTCCA[C/T]GTCAACACGGATGAT | 9690 |
rs531805225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140312 | AAGGAGGAACTGCTG[A/T]TATTAAGATTGTGCT | 9690 |
rs531838527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201064 | TGCAGTGGCACACAC[C/T]TGTAATCCCAGCACT | 9690 |
rs531857187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181908 | ACTGTCAAAAATTAA[C/T]GAAAACATGGTAGTT | 9690 |
rs531864708 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185949 | CAATACCCAATGTTA[C/T]ATATATTCACATTCA | 9690 |
rs531900299 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194180 | ATCTTTTTGAAATGG[A/G]GCTGGCTGTTATACA | 9690 |
rs531976264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157158713 | ATACTCTGAACTCAG[C/T]TAATCCTTTGCTTTG | 9690 |
rs531999521 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157179827 | ATACTCATTTCAGCC[-/T]TGCTGCTTGGCGTGT | 9690 |
rs532003741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247763 | CAAATTTGGAACATA[A/G]CCACCCTCACTCATT | 9690 |
rs532017377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242234 | GCAGTCAGTATCAAT[C/T]GGAGTTCATGGATGC | 9690 |
rs532055046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242802 | TGGCTCAAGCCTGTA[A/G]TCCCAGCACTTTGGG | 9690 |
rs532066540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200257 | TTTTTCAGTGATGTA[C/T]CCTTATTGCCATCTG | 9690 |
rs532077078 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258589 | CTCAGCCTCCTGAAT[A/G]GCTGTGATTACAGGC | 9690 |
rs532086089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241530 | TGCCGCGCACACCCG[C/T]GAGTACGGCGGGAAT | 9690 |
rs532087426 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191599 | CACTGCGCCCAGCCC[C/G]TCGTGTGTTTTCTAA | 9690 |
rs532089731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213099 | TAGTACTTGAATAAT[A/G]TATTAGTTTCTGCAT | 9690 |
rs532090159 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157157425 | ATGAAAAAATTAAAT[G/T]ATTCAAACTGTGGAA | 9690 |
rs532113975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240067 | AGGGCTCAGCAAGCT[C/G]TGTGTTTTGGTTTTT | 9690 |
rs532124777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194308 | GGGCTCACCACTTCC[A/G]TCCTGTGGTAGTTCT | 9690 |
rs532173452 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214601 | AATCTGGATTTATTT[A/G]AAGTATCAATTTAAT | 9690 |
rs532178118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175923 | GGGTTTGTGGTCCAC[A/G]TATGGTCTCTATTAT | 9690 |
rs532189381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207235 | TATGCTGTTTATTAA[C/T]CTGCATTGCCATGGT | 9690 |
rs532203642 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173239 | TAAATTAGCTGGCTG[C/T]GGTAGCTTGCTGCTG | 9690 |
rs532209108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247387 | GTAACTGTTGTCTCT[A/G]TTGTCTTTATTAGAA | 9690 |
rs532216719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140344 | TGGGGCTGTGTTTGG[C/T]GGTTTCTGAGGTTAG | 9690 |
rs532224041 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235234 | CTTTACAATGAAATC[C/T]CTTAGTTCTTTCTGT | 9690 |
rs532229707 | snp | A/G | 0.000163412 | 0.00903766 | intron-variant | UBE3C | GRCh38.p7 | 7:157164489 | GAAGCATAAGGAGAA[A/G]GCTCACTGTTAAGAC | 9690 |
rs532243454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145443 | GAATTGCTTGAACCC[A/G]AGAGGCAGAGATTGC | 9690 |
rs532247490 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157232423 | GAGTGCTGTGGCGCC[A/G]TCTCTGCTCACTGCA | 9690 |
rs532257267 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157264654 | TGCGTGATCTCGTCT[A/C]ACTGCAGCCTGCAAC | 9690 |
rs532264705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157163986 | GACAGAATGTGTGTG[G/T]ATGTGTGTTTAGCTT | 9690 |
rs532274887 | in-del | -/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137272 | GACAGAGTCTCACTC[-/T]TGTCACCCAGGCTGG | 9690 |
rs532301262 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204858 | TAGTATTCTGAAAAC[C/G]TGTTAAAGCAAGAAT | 9690 |
rs532320848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193370 | CTGTTTCTTTTACCT[A/G]TGGCACCTGGACTTA | 9690 |
rs532333070 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157220918 | ATGTAGAAAAGTTTC[A/G]TCACCCACAAAATTG | 9690 |
rs532334451 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157171257 | TCAGCCACCTAAGTA[G/T]CTGGAATTACAGGCG | 9690 |
rs532371697 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157226827 | TAGGTCTGCATGCAG[A/G]CTGTGGCCTCTCCAC | 9690 |
rs532373173 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237130 | GTATTCCTGAATTCA[C/G]TTGATTGCTGCACCT | 9690 |
rs532384492 | snp | C/T | 3.29652e-05 | 0.00405974 | intron-variant | UBE3C | GRCh38.p7 | 7:157201828 | TATTATACAGACTTA[C/T]AAATTGAGCTCAAGG | 9690 |
rs532417529 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258466 | TTGTTTGTTTCTTTG[C/T]TTTTGAGACGGAGTT | 9690 |
rs532429505 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256051 | CTTTGAACTGCAGCA[C/T]GGTTCTTCAAAATAA | 9690 |
rs532442254 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157152230 | GAAGGTAGTCAGGGA[C/G]AGAGCTGGGGGAAAG | 9690 |
rs532469821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254538 | GAATAGCTGGGATTA[C/T]AGGCACCTGCCACCA | 9690 |
rs532494697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188393 | TCTTCACTCACTGGT[A/G]TTTATTACCATCGGA | 9690 |
rs532503582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247822 | TGCAGGGCAGAGTGG[C/G]ATATGCGGTTATGAA | 9690 |
rs532543540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208968 | CGCACACTAATGTTC[A/G]GTTCGAGTCATCAGC | 9690 |
rs532550172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239163 | ATGTGAAAGAATGTT[C/T]ATGGTAACACTGTAT | 9690 |
rs532552429 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198399 | TTTGGCTGTTTTCAA[G/T]TTTCTTTGCAGGTTC | 9690 |
rs532572259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157208131 | CCAGGCTGGAGTGCA[A/G]TGACACCATCATACT | 9690 |
rs532577100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196250 | ACTGATGTTAAAAGC[A/G]CCGCGAAACCCGTTT | 9690 |
rs532578695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215752 | AATCCTGGTTGTAGA[C/T]ATTTAAAATGTTGGA | 9690 |
rs532610282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215204 | GCTCGAATAACACTT[C/T]TTCTCTGTCCACGGG | 9690 |
rs532671515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176344 | CAGTGGCGTGATCTC[A/G]GCTCACTGCAACCAC | 9690 |
rs532685769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165809 | TTAATTTCTTGAACA[G/T]AATTATAGATTTTTT | 9690 |
rs532702847 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177035 | ATATTTTTTAATGCC[A/G]TTGAACATTTCTGAA | 9690 |
rs532726899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173760 | ATAGAAATTTTAGGA[C/T]GAACTACATGTCAGA | 9690 |
rs532808488 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266986 | AGCTCAAGCCATCCC[C/T]CAGCTAGGCCTCCCA | 9690 |
rs532810354 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244229 | ATAGAGTGAAACTCC[A/G]TCTCGAAAAAAAAGA | 9690 |
rs532818483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243158 | CAGGAGATGTGCACG[C/T]GTCCTCCACGGTCCC | 9690 |
rs532822356 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264488 | ACACACCTGGTACTA[C/T]AGGTGTGCGCCAACA | 9690 |
rs532823123 | in-del | -/T | 0.0744748 | 0.178019 | intron-variant | UBE3C | GRCh38.p7 | 7:157236729 | TTGAACCCTAAACTC[-/T]TTTTTTTTTTCTCTT | 9690 |
rs532828046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250780 | CATCCAGTGATGTCG[C/G]TTGCTGCTAGGTCTT | 9690 |
rs532858717 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137864 | CGACCGTGCTCGGCC[A/G]CAGGACGACTGTAGA | 9690 |
rs532860044 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161456 | TTCTTTGATTTTACT[-/T]TTTTTTTTTTTTTGA | 9690 |
rs532861009 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157173279 | TACTTAGGAGGCTGA[G/T]GCAGGAGGATCGTTT | 9690 |
rs532867060 | snp | A/C | 1.65135e-05 | 0.00287341 | intron-variant | UBE3C | GRCh38.p7 | 7:157256894 | TGCATTTCATAAAGC[A/C]TGTGTTCATTTTGCC | 9690 |
rs532907272 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227504 | GAGATCGAGACCAGC[C/T]TGGCCAGCATGGTGC | 9690 |
rs532981957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157244921 | GGTACAGCTGGCTGA[A/G]AAGGCCAGTGTGAAA | 9690 |
rs532982759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218206 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCAAGTG | 9690 |
rs532986905 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157211361 | TCCAAAGCTTGTAGC[A/G]CTGTGCCTTATCCTT | 9690 |
rs532997187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198545 | GTCTTTTTTTTTTTA[C/T]TTTTTTCGACAGGGA | 9690 |
rs533007701 | in-del | -/T | 0.00283286 | 0.0375287 | intron-variant | UBE3C | GRCh38.p7 | 7:157159477 | TTCAAAAGATCAGAC[-/T]GTGGATGGTTTCTTG | 9690 |
rs533011472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198006 | TCCTGATGGTCCTCC[A/G]TATCCCAATTCACTT | 9690 |
rs533023425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217817 | ACTCCAGCCTGGGTG[A/T]TAAGAGCGAAATTCC | 9690 |
rs533062689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217503 | TGAATATTACTAATA[C/T]CTACATCTAAAGCAG | 9690 |
rs533079809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167831 | ATGAGCCACCATGCC[A/T]GGCCTAAAGTGCCTC | 9690 |
rs533094375 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186742 | CTAGCTTTCTTTGCC[C/T]GAAGAAAAATGTGAT | 9690 |
rs533146718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180167 | TACTTTCTAACAGTC[A/G]ATAAAATTTTAGCCT | 9690 |
rs533154972 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139043 | TGTGGCCGGCGTGGA[A/T]GAGGGGCAGGCGAGG | 9690 |
rs533195871 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231653 | GGCCCTGGTGACTTT[G/T]TACAGGAGGGAGCCC | 9690 |
rs533212410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240904 | AACTGTGTGCTACAG[A/T]TGTCACCAAAAATTA | 9690 |
rs533224935 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268680 | CACTTGTCTTCCTGG[A/G]TATTTGGGGGTGACT | 9690 |
rs533277579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157161843 | TCGGGAGGCCAAGGC[A/G]GGCAGATCACTTGAG | 9690 |
rs533278816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240492 | TATCATAAAGTGAAG[G/T]GAGACCAGCCGTGTG | 9690 |
rs533290863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157192692 | TTAGAAGGTGGATGA[A/G]AATGACAAAATGAGC | 9690 |
rs533330998 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157160694 | CTATATCTTGAGAGA[G/T]ACTTTGAGACTAGGC | 9690 |
rs533361500 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157179472 | GAGGACACATTAGTG[A/C]CACTTTCTGGAGAAA | 9690 |
rs533386551 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157152874 | ACATCTTTTGGAACT[-/A]ATTTTTCTTACAGTG | 9690 |
rs533389645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257915 | GTGCTTATGAAACTT[C/T]ATAGGCATTCACTTT | 9690 |
rs533440663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209351 | GTTGAATTTATAATT[C/T]GGGCAGATTGATGTA | 9690 |
rs533471982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156575 | CCTCCAAAACTGCTA[A/G]CGTTACAGGCATGAG | 9690 |
rs533482720 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188188 | AAAAGCTGTCAGTAA[A/G]TAAGCAGGTCTGACG | 9690 |
rs533491751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174578 | CCATCTCAGCCTCTC[A/G]AATAGCTGGGACTAC | 9690 |
rs533523510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157141388 | ACTTAAAGAGGGGGA[C/T]GCTGTCACTAGTCCA | 9690 |
rs533526379 | snp | G/T | 1.6617e-05 | 0.00288239 | intron-variant | UBE3C | GRCh38.p7 | 7:157169149 | TTAAAATGAGGAGAT[G/T]AGTAGGGCATGGGAG | 9690 |
rs533537791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191516 | GGCTGGTCTCGAACA[C/G]CTGGGCCCAAGTAAT | 9690 |
rs533539835 | in-del | -/C | 0.0260207 | 0.111055 | intron-variant | UBE3C | GRCh38.p7 | 7:157187663 | TCACTGTAGGCTCTG[-/C]CCCCCTGGGTTCATG | 9690 |
rs533555770 | snp | A/G | 5.07421e-05 | 0.00503671 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267735 | GCGATTGAATGTGCC[A/G]CTGGCTTTGAGCTGA | 9690 |
rs533601046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204875 | GTTAAAGCAAGAATC[C/T]GTTCTTAAAAGCTCT | 9690 |
rs533610669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245159 | GTTTAAACCTGCCTC[A/G]TGTAAAAAATGGTAC | 9690 |
rs533629032 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227566 | ATAGCTGGGCGTGGT[C/G]GTAGGCACCTGTAGT | 9690 |
rs533630623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251922 | GGCAGATCATTTGAG[A/G]TCAGGAGTTCAGACC | 9690 |
rs533638507 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157162001 | CTTGAAACCGGGAGG[C/G]AGAGGTTGCAGTGAG | 9690 |
rs533647325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157139586 | AGGACTGGACTCGGG[A/G]CCTCCCTGGCTGGAA | 9690 |
rs533663587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157238495 | GATGTTGGGATGTGT[A/G]AGGACAGGAGAAGGT | 9690 |
rs533668328 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157252558 | GAACGTTCAAGTTCA[A/G]TTTGAACATTCTGTA | 9690 |
rs533674694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167598 | GCTGGAATGCAGTGG[C/T]GCGATCTCGGCTCAC | 9690 |
rs533678511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175166 | TTTTTTTTGAGGTCA[C/T]GGACTTCTGTATATA | 9690 |
rs533688694 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142833 | TGCATAGGTACCCCC[-/T]AACTCTAAAATAAAA | 9690 |
rs533690214 | in-del | -/TC | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157233113 | TGGATTTTTTTTTTT[-/TC]CTAGACATTTCATAT | 9690 |
rs533743368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186084 | AATCAAATCTTCTGG[A/G]GAGATTAAGGTATAA | 9690 |
rs533829542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204596 | GGATAGTGAATTTTG[A/T]CACATCAGACATTTT | 9690 |
rs533845423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197546 | GGAGGTATTGTCCTT[A/C]TTAATACGACACATC | 9690 |
rs533853596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239859 | GAACACTGGGTGCAG[C/G]TGCATGAGCTGGGGA | 9690 |
rs533862033 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157154804 | AAGAAATCTATAACT[G/T]GTTGTAGTCAGACTT | 9690 |
rs533882746 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268294 | TGGAAAAGAGATGAT[A/G]ATGGTAATATTTTAT | 9690 |
rs533932180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205954 | AATTAGAACAAGTGG[C/T]CTTACCTTCTGCTTT | 9690 |
rs533949026 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157658 | TTAGCCAAAAACTGA[A/G]AACAACCTAAATGAC | 9690 |
rs533965325 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244451 | ATGGTTAATATGATA[C/T]GAAATAATTAAAATT | 9690 |
rs533965410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205462 | AGGATTCTTGTCGGG[A/G]ATAACAGTGGAAAGC | 9690 |
rs534003058 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138349 | TATAGATGCATATGT[C/G]TGCTATGTATGAGGC | 9690 |
rs534027905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144029 | GACACAGTGAGTCCA[C/G]TGACTGCGGAGCTGG | 9690 |
rs534042647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218661 | TGGGGTTGCTTCACA[A/G]CAAAAGAAGCAGTCC | 9690 |
rs534061584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230164 | ATCCGCCCACCTCAG[C/T]GTCCCAAAGTGCTGG | 9690 |
rs534064029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174085 | GAGGCTATCTTTGCC[C/G]AGGGTGGTGGCTCAC | 9690 |
rs534067471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143426 | AAACACCCAGATAGC[A/T]GGTATCACCACCACA | 9690 |
rs534067491 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159865 | ATCTAATTACAGACA[C/T]GTAAATCAGAATTCT | 9690 |
rs534070029 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157190559 | ACACACCCACCCTCA[C/T]GGAAGGTGCTGGTGG | 9690 |
rs534077185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224015 | TATCAGAAACGATGT[G/T]TTTTTTTTTCTGAGA | 9690 |
rs534081405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157150462 | ACGTAAAAATTTATT[C/T]TAGTGAACTAATATG | 9690 |
rs534100259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157229748 | TCCTCTTGAGTAGCT[A/G]GAATTACAGGCACAT | 9690 |
rs534116752 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186346 | ATTGCTTGAACCTGG[C/G]AGGCGGAGGTTGCAG | 9690 |
rs534143469 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157192292 | GTTTTTAAAGTTTTC[A/T]TTTAAGCTTGTTAAG | 9690 |
rs534145844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262054 | TTAAGCTTTTCATTT[A/T]TCCAGTGACTTTGCC | 9690 |
rs534152650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193062 | TGCTGGAATGCTAGC[A/G]CGCCTGAGTGTCTAA | 9690 |
rs534165541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151183 | TAATCCTGAAGCCAC[C/T]GTAGAAGGGAGCTTC | 9690 |
rs534177852 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189402 | AAATATTCACTGGCT[A/G]TATTTTAAGGGGGCA | 9690 |
rs534180690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157246185 | CATGCCCTGTTGGAG[C/T]GTATAAGTTCTGGAA | 9690 |
rs534182985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157199842 | TACTTAGTTACCTGT[C/T]TTAATTGGTCTCCTT | 9690 |
rs534243359 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242053 | TTTAGAATAATGAAA[A/G]TCTTCAGAAATTGAT | 9690 |
rs534257123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257987 | AGCACTCGCTGTATC[A/T]CCCAGGCTGGAGTGC | 9690 |
rs534269265 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219299 | AGTGATTTAATTGAT[A/T]TATATTTTGGCACAA | 9690 |
rs534291298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174699 | TCAGGTGATCTGCCT[A/G]CCTCAGCCTCCCAAA | 9690 |
rs534292969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171468 | ATCCCAAATGTAATC[A/G]TAGTTCTCTAAAATT | 9690 |
rs534302464 | snp | A/C | 0.0279526 | 0.114869 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138654 | CCCCTCGCCGCGCTC[A/C]CCCAGCACGCACCAG | 9690 |
rs534304540 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141829 | CTGAGAGGTGGACTC[C/T]ATCCGCCTCGGTGCA | 9690 |
rs534331454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177104 | CACTTTAGAAGAAAC[C/T]ACCAAACTTAGGACA | 9690 |
rs534346304 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235930 | TAGTGTGGCACCTGA[A/T]CATTACATCTTCAAG | 9690 |
rs534348461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216237 | AGTGCCGTTAGTACA[C/T]TATTTCTCAGAAAAC | 9690 |
rs534348504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208611 | ATTTCTTAGATTTTA[G/T]TGTTTTTTCAAACCT | 9690 |
rs534357947 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157237072 | TCTTCAGAATTAACC[A/G]TGAAATACAAGTGGT | 9690 |
rs534360235 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268942 | TCATTTATCTCTTCT[A/G]TGTCTCGTATTTTAC | 9690 |
rs534403689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206409 | CTGGGATTACAGGCA[C/T]GTGCCACCACACCCA | 9690 |
rs534411207 | snp | G/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207449 | TTCTCCTATGTCTTT[G/T]GAAGATTCTAGTCGA | 9690 |
rs534433621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157529 | TCTCCTTGGAGGGCA[A/G]TTTGGAAATATTCAT | 9690 |
rs534483411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157199818 | CTCGAACATTAATGA[C/T]AGACAGCATACTTAG | 9690 |
rs534536898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202703 | CCCCTGTGCTGTAAT[C/T]GGAAAAGATGAAGTG | 9690 |
rs534572776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165484 | CTCACTGCAACCTCC[A/G]CCTTCCAGGTTCAAG | 9690 |
rs534593225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247987 | TGGTTTTCAGTCTCG[A/C]AGTGTGTGATCATTT | 9690 |
rs534620344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171038 | GCTGGTCGTGAACTT[C/T]TAGCCTCAAGTGATT | 9690 |
rs534655022 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156656 | GGATTTTTACACATC[C/T]TGTCAGAGCTGTTCT | 9690 |
rs534682827 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167262 | TAACCATTTCAAGCC[C/T]AGGAACTACATCTAC | 9690 |
rs534723338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157141036 | CAGGAGCATGCTACA[A/G]TTGGCCCTAATTGCG | 9690 |
rs534730487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261142 | ACCCCGCCTCTACTA[A/G]ATACAAAAAAAAAAT | 9690 |
rs534771711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160312 | ACTCCTGACCTCAGG[C/T]GATCTGCCGGCCTTG | 9690 |
rs534793708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148169 | GGAGTACAGTGGTGC[A/G]ATCTCACTGCCACCT | 9690 |
rs534812661 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222408 | CCTTCACCTAACACT[C/T]TACTTTTTTTTTTTC | 9690 |
rs534813351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157233952 | GTGACTAATAATGTT[C/G]ACCATCTTTTCATGT | 9690 |
rs534818280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197550 | GTATTGTCCTTATTA[A/G]TACGACACATCATCT | 9690 |
rs534828574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154094 | GGAGGGAGGCCGAGG[A/T]GGGTGGATCACGAGG | 9690 |
rs534865959 | in-del | -/CAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244503 | GGCTTTAAAGCAAGA[-/CAT]CATCTCTTATATAGT | 9690 |
rs534904328 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240047 | GAATCTGGAACTCTA[A/G]GGCTAGGGCTCAGCA | 9690 |
rs534925577 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242911 | AATACAAAAATAAGC[C/T]GGGCGTGGTGGTGGT | 9690 |
rs534934441 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258910 | TGCTACATTTACTTT[A/G]TCATTCTTTTCATGC | 9690 |
rs534957213 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263094 | ACATCTCTTTATATC[C/G]AGCATCCTCTTACAT | 9690 |
rs534977359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217529 | AGCAGATTCAGTAGT[A/T]TGATACGTTAGTAAA | 9690 |
rs534982874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157177772 | GCCTGCGGTAAGCGG[A/G]TAAGCCGTGTAGACA | 9690 |
rs534985662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184471 | CTTTTCTTCCTTACT[A/G]TTGAGTTTACAGTAT | 9690 |
rs535000730 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137031 | AAGCTCCGCCTCCCG[A/G]GTTCACGCCATTCTC | 9690 |
rs535002153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267060 | TGTTATTTATCCCTT[C/T]TTATGCCTGAAGCAC | 9690 |
rs535015348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223433 | ACCAGAGAAATCTCT[A/G]AAGGTGCCTAGTGCC | 9690 |
rs535022918 | snp | A/C | 8.25893e-05 | 0.00642556 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183881 | TGTTTTGCAAAGGGG[A/C]CCTCTCTGAGGAAGG | 9690 |
rs535062307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157222883 | TTGCCATAGTAGGAG[A/G]GAAAGGGCACGAAGG | 9690 |
rs535063063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157166539 | TGAGGTTGGGAGTTC[A/G]AGACCAGCCTGACCA | 9690 |
rs535106885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202478 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 9690 |
rs535132122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209953 | TGGGAGGCCAAGGCG[G/T]GTGGATCACGAGGTC | 9690 |
rs535229579 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157203813 | AATACAGATACTCCT[A/T]GAGGTACAATGGGGC | 9690 |
rs535254853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244509 | AAAGCAAGACATCAT[C/T]TCTTATATAGTTTTT | 9690 |
rs535259166 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264694 | CTGCCTCAGCCTCCC[A/G]AGTAATTGGAATTAT | 9690 |
rs535357026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172458 | CCATCCCTACTAGAA[A/T]GATCCTACTTGAATT | 9690 |
rs535396244 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157159839 | AAAAATAAATACCAT[A/T]TGCTTGCCTGATCTA | 9690 |
rs535441781 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138155 | TAAAATGGCTCAACT[C/T]ACAATTTTTTGACTT | 9690 |
rs535442216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248911 | GCTTCCCGGCAGGAC[C/G]CCTTGCTTAGTCCTC | 9690 |
rs535478794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157243868 | GTGGTCCCTGACATA[C/T]AGTTGGCACTTAATA | 9690 |
rs535498927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209426 | CTAAGTAAACTGGGA[C/T]GGTCACATGGTAAGC | 9690 |
rs535504622 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137471 | GGGGTTTCCCCATGT[C/T]GGCGAGGCTGGTCTC | 9690 |
rs535505427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248689 | CCGCACATTTTAGTT[A/C]GAATGACTGTGGCTG | 9690 |
rs535527166 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157166128 | GTGTTACCAATACTT[C/T]GAATATTTTATTGCT | 9690 |
rs535538184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157216347 | AGACATTTCCAGATT[C/T]GTGGGTTTTTTTTTT | 9690 |
rs535563630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157171799 | GTAACCTCCGCCTCA[C/T]GGGTTCAAGCGATTC | 9690 |
rs535571172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229024 | CTCCAGGGCAGATAT[C/G]TTTGGGTGACTATGC | 9690 |
rs535613239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184591 | TTTGGTCTTAAGCAA[C/T]TGAAATGGCTTGAGG | 9690 |
rs535625332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266594 | GTTTAATGTGCTTCT[A/G]AAACAGCCGTGTTCT | 9690 |
rs535627815 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157171010 | GAGATGAGGTCTTGC[-/T]TATGTTGCCCAGGCT | 9690 |
rs535629103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157162076 | TCTGTCTCAATTTAG[A/G]AAAAAAGGATAGAAA | 9690 |
rs535652669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245516 | AACTGTGACTTTTCA[A/G]CACAACTTTCTTTAC | 9690 |
rs535672219 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214312 | CTCATATAATTTGAT[A/G]ATGTTTGTAATCTGT | 9690 |
rs535685696 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179813 | CAGAAATTAAACGCA[C/T]ACTCATTTCAGCCTT | 9690 |
rs535686857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157246051 | TCATTTTCTGAAACA[A/G]AAAGCCAGTGGTACT | 9690 |
rs535693628 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201806 | ACACGGATGATCACA[A/G]GGTATGTATTATACA | 9690 |
rs535727038 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157154137 | ACCAGTCTGGCCAAG[A/T]TGGTGAAATCCCGTC | 9690 |
rs535734373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250440 | GATCCTCCTGCCTCA[A/G]CCTCCCAAAGTGCTG | 9690 |
rs535737951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211530 | TTGTGCCAGAGGTTG[C/T]GAATTTTTTGTGTGA | 9690 |
rs535763814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167607 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 9690 |
rs535858156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258755 | ATGAGCCATCATGCC[C/T]GGCCCCCCAAGTATT | 9690 |
rs535864830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157249749 | GACATTTGGGTTGTT[C/T]CTATGTTTGGGCTAA | 9690 |
rs535886169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157217602 | AGCACTTGGGGAAGC[C/T]GACGGGCAGATCACT | 9690 |
rs535889324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226341 | GGCACGTTTCGTCGT[A/G]TGTTCATATTTGATA | 9690 |
rs535893646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157252985 | GATCCTCTTGCCTTG[A/G]CCTCCCACAGTGCTG | 9690 |
rs535910105 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219935 | GCAAGGGCCAGCCGG[C/G]TGTGGTGGCTCACGC | 9690 |
rs535922487 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157225819 | ATCTGGATGTGTTAG[C/T]GTGCCCCTGTTGTCC | 9690 |
rs535965949 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157144619 | GGAACTGAAATTTTT[A/T]AAGTTTTTGTAGATC | 9690 |
rs535972510 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239477 | GGCTTCCAAGGTGCT[A/G]GGCATTTTCTGCGCT | 9690 |
rs536001501 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190843 | AACCATAAATGAGGC[-/A]AAAAAGGCATATCTT | 9690 |
rs536018030 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230581 | ACGCCTGTAGTCTTA[G/T]CTACTTGGGAGGCTG | 9690 |
rs536024224 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162778 | CTGCCTTGGCTTCCC[A/G]AAGTGCAGGGATTAC | 9690 |
rs536046683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198194 | TAGCTGATTTTCTCC[A/G]TGCATATATTCAGAC | 9690 |
rs536075395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157247874 | CTCAAATCCTAATAC[C/T]CCATCCTGTGGGCAC | 9690 |
rs536075428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242358 | GAAGGCATCATTGTC[C/T]TCAAATTTCTCAAGA | 9690 |
rs536080489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204771 | ATAGAGATGCTTTGC[C/T]CAGATGTCTTCAGTG | 9690 |
rs536154444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140422 | TCAGCTTTGAGGTTC[A/G]TGTGATGGTGATTGC | 9690 |
rs536159422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214243 | TATTGAAATTTTTTT[A/G]ACATTTAATTGTATA | 9690 |
rs536180178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157169639 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAAG | 9690 |
rs536217808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175458 | TATTTATGTAGGAAC[A/G]CAGCATAAGCCACTG | 9690 |
rs536221665 | snp | C/T | 0.000197772 | 0.00994217 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182192 | CATCATTCCGGCGCT[C/T]GCAGATGCGCAGACC | 9690 |
rs536263391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259259 | GGCCGGTTGTCCCTT[C/T]GCGTCCTTCATAGAA | 9690 |
rs536287312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153022 | CCAACATGGCGAAAC[C/T]CTGTCTCTACTAAAA | 9690 |
rs536308296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144924 | TGTGTAGGTTTTGAC[A/G]AATATATGATGACAT | 9690 |
rs536322079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158951 | AAGTCTGCTCCCTTT[C/T]TGTATTGAAAACACA | 9690 |
rs536361243 | snp | C/T | 0.00119832 | 0.0244484 | intron-variant | UBE3C | GRCh38.p7 | 7:157165398 | CTCTTTAGCATTGAC[C/T]TTTTTTTTTTTTTTT | 9690 |
rs536370067 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168748 | AATAAGCACATCCAT[A/G]AGATAGAAGTAGATG | 9690 |
rs536386487 | snp | A/G | 0.000809061 | 0.0200967 | intron-variant | UBE3C | GRCh38.p7 | 7:157187662 | CTCACTGTAGGCTCT[A/G]CCCCCCTGGGTTCAT | 9690 |
rs536396171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264179 | CCAACATGTTCGGCC[C/T]GTTAAGCACAGAGAC | 9690 |
rs536396829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164951 | GATTTTCCAACCTTG[A/G]TGCTGACATTTTTGA | 9690 |
rs536421218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224619 | TTTTATTTGTCAACT[A/G]TTTTTACCAAATTTC | 9690 |
rs536449808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201316 | GCAACAGAGCAAGAC[C/T]CTGTCTCAAAAAAAA | 9690 |
rs536478699 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153062 | TTAGCCAGGCATGGT[A/G]GTGGGCGCCTGTAAT | 9690 |
rs536486646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207628 | ACAGTAGAAAAGTTT[C/T]AAGCTTTTTAAGTCT | 9690 |
rs536542260 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248132 | TAATTCCACGATTTC[A/G]CTCCTAGGTGGTCTG | 9690 |
rs536588846 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157259697 | TTTAGAGACACAGAG[C/T]GGGTCAGGGGCTGCA | 9690 |
rs536593658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157265724 | TTAAACCTAAAGGAG[A/G]GAGAACATTTTCTCA | 9690 |
rs536610310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175541 | TTACATTACCTGAAT[A/G]TAACACCTTTACCAG | 9690 |
rs536673742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157195289 | ACCCACAAGTTTCTC[A/G]ACAATGTTATAGCAG | 9690 |
rs536682907 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149060 | TAAGGTTAAGAATTC[-/T]TTTTTTGTTTTTTGA | 9690 |
rs536699563 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194668 | AGCAGAGAATACCTC[A/G]ATTGCGGTAAAATAT | 9690 |
rs536706774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201903 | TTTTAAGTCCTGTTT[A/G]TACTGGGCTTATTTC | 9690 |
rs536741806 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157238384 | GGAGACCGGATGGAG[G/T]GTCACATCGTTCAGG | 9690 |
rs536752304 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146266 | TTTTTTTTTGAGACG[A/T]AGTCTCGCTCTGTCT | 9690 |
rs536755802 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160221 | CTGAGACTACAGGTG[C/T]GCGCCACCACGCCCA | 9690 |
rs536811805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238398 | GTGTCACATCGTTCA[A/G]GTGGAGTGATGCTGC | 9690 |
rs536845027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202342 | AGCCTAGTACTCTGT[G/T]GTTGAATTTTTCCTC | 9690 |
rs536924122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227590 | CTGTAGTCCCACCTA[C/T]TCAGGAGGCTGAGGC | 9690 |
rs536926151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221455 | TAAAAAAAAAAAATT[A/C]TATGGGCCAGGCGTG | 9690 |
rs536949161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157242935 | TGGTGGTTGCCTCTA[A/G]TTCCAGCTACTTGGG | 9690 |
rs536979590 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157164997 | TTGGGGGGAACTGCT[C/G]TGTACATTGGAGGAT | 9690 |
rs537065260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260175 | CTCTGTTTACCAGAT[A/G]TGGGGGGTGGGGGTG | 9690 |
rs537068805 | in-del | -/AC | 0.192781 | 0.243364 | intron-variant | UBE3C | GRCh38.p7 | 7:157264242 | CTCGGCCTGTTACAC[-/AC]ACACACACACACACA | 9690 |
rs537077804 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254976 | CTGCAGTCCCGGCGT[C/G]GTGGCGTACACCTGC | 9690 |
rs537091632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147453 | GAATTTCCTGCACAG[A/G]TAATCATTTCATTTG | 9690 |
rs537093909 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157259309 | TTGCATTTAATTGGC[A/G]TGCTCTTTAGTTTCC | 9690 |
rs537106972 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157140482 | TACTGTGCAGTTAAG[A/G]GTGGTCGTGGTAGCA | 9690 |
rs537122853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238785 | AACTGAGCCCCAGGG[C/G]TCTCCAAGGTTTAGA | 9690 |
rs537129074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157146925 | CAAAGTGCTGGGGTT[A/G]CGGGAGTGAGACACC | 9690 |
rs537130877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153657 | TTATCACGAATCTTC[C/T]TTGCTCTAAGAATGG | 9690 |
rs537167884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153103 | TGGGAGGCTGAGGCC[A/G]GAGAATGGCTTGAAC | 9690 |
rs537170204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157159596 | TTTGCAGCTGGGTGC[A/G]ATGGCTCATGCCTGT | 9690 |
rs537234894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157255503 | AAGCAAATAATGCCT[A/G]AGGTCACGTTGTCCC | 9690 |
rs537255419 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217878 | AATACAAATATTAGC[C/T]GGGCATGGTAAGTGT | 9690 |
rs537260048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177736 | CTCTCCTGGGCTTTG[C/T]GGCTGTTGAGACAGA | 9690 |
rs537291889 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137022 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 9690 |
rs537302798 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157260636 | AGACAAGGCTTCTAG[C/T]ATCTTTGTTTCAAAA | 9690 |
rs537303684 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261536 | TTGTTATATGTTAGA[C/T]ATCCAGTTTGGAAAA | 9690 |
rs537344846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237428 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 9690 |
rs537347344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165461 | GGACTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC | 9690 |
rs537367492 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237650 | TTTCTGGGCCATGTT[A/G]ATTTGTCACCATGAA | 9690 |
rs537379205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170962 | CAGGTGTGTGTACAC[C/T]TTGTTAATGTTAAGG | 9690 |
rs537403507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227654 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 9690 |
rs537405214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157153906 | GCTGAGGTGGGAGGA[C/T]GGCTTGGTGGGGCGG | 9690 |
rs537456916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192349 | TCGATCCGCCATCTG[C/T]GGTGGAGCCGCCACC | 9690 |
rs537464699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262898 | CTGCAGAATGGGACA[C/T]TGCTCTAGTTTGATT | 9690 |
rs537488743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150542 | CTGAAAAATACTGAA[A/G]CAGCCTACATGTCTA | 9690 |
rs537497178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195928 | CCATGTAAAACGTTA[A/G]TGTCCTAATCTCCAA | 9690 |
rs537501422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189270 | AATATTTTAAAATTG[G/T]TTAAGTAATAAATGA | 9690 |
rs537527671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149856 | CTTTGACTGTGACCC[C/T]TGTTTTTTACTGCCT | 9690 |
rs537527751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156337 | TTTGAGACAGAGTCC[G/T]GCTCTGTCACCTGGG | 9690 |
rs537529569 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206420 | GGCACGTGCCACCAC[A/G]CCCAGCTAATTTTTT | 9690 |
rs537532806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235958 | AAGAGAAGAAAACTG[C/T]ATATTGATTGATTGT | 9690 |
rs537564677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157155797 | AGTACCTAAAGCTCC[A/G]CAGGCACCCAGAGCA | 9690 |
rs537660421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174237 | CGTGGTGGCGGGCAC[A/C]CGTAATCCGAGCTAC | 9690 |
rs537671267 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157252077 | GATGGTGGAGGTTGC[A/C]CTGAGCCAAGATTGC | 9690 |
rs537677577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248954 | CTCAGAGCCACCTCA[G/T]CTGCTCCAGCACTGT | 9690 |
rs537706599 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138758 | CCGCGCACGCTAGCG[C/G]AACCGCCGGGAAGAG | 9690 |
rs537754743 | snp | C/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157144054 | AGCTGGGAAGAATTG[C/G]GTGATTTGAGCATAT | 9690 |
rs537768137 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157141651 | ATGTGGTCTGTTGTC[A/G]ACAGACTGAGAGGTC | 9690 |
rs537796915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157177311 | CTTTTTCAAGAGTCT[A/G]TTCAAATCTTTTACT | 9690 |
rs537841538 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157153843 | AACAAACAAACAAAA[-/C]AAACGGGCATGGTGG | 9690 |
rs537850246 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157227550 | AAAAATACAAAAAAA[A/T]ATAGCTGGGCGTGGT | 9690 |
rs537864340 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268784 | GGGAAGAGGAGTGTC[A/G]GTAGTTCTTGCAGTA | 9690 |
rs537875219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199893 | TTTTCGTTTTTCCAA[C/T]ATTATTAAATATTTA | 9690 |
rs537887917 | in-del | -/ATG | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157171757 | GTCACCCAGGCTGGA[-/ATG]ATGCAGTGGCATCAT | 9690 |
rs537890412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198754 | TGACCAGGCTGGTCT[C/T]GAACCCCTGACCTCA | 9690 |
rs537938480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157169501 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 9690 |
rs537962601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162695 | CGGGCACATACTGCT[A/G]CACCCAACTATTTTT | 9690 |
rs537972385 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157235299 | TATGTGAAAATAAAG[C/G]TGAGTGTTCTGCTAG | 9690 |
rs537987935 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246101 | AAAACCTCAACAGCT[A/G]TTTTCTCATTTTCTC | 9690 |
rs538007687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225843 | GTTGTCCCTGCTCTG[C/T]AAAAGGCTGAGGCGG | 9690 |
rs538039182 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157144841 | TACAATTGATAAACC[A/C]ATGTCGATGTGTTAT | 9690 |
rs538040444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181390 | GTTTAGTTTTCCTTG[C/T]TAGCATGTTAAAGAA | 9690 |
rs538055103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180452 | GGTTAGACTTGGGGT[A/G]GTTACAAAGTAGGTC | 9690 |
rs538089816 | snp | A/C/T | 0.00893228 | 0.0662325 | intron-variant | UBE3C | GRCh38.p7 | 7:157139386 | CGGGGCCTGCGCGGC[A/C/T]GGGGCTCGGGGCTGG | 9690 |
rs538095791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257466 | TAATGTTGATCTTAC[A/G]TAATTTGGCTTATTT | 9690 |
rs538103160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193957 | CTATTATTTACAAAA[A/G]TGGCAGTTGTTTTTG | 9690 |
rs538114515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218809 | AGGAGCCTGTCTCTA[A/G]CTGGTCATGGGCAGA | 9690 |
rs538145837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231469 | CAAAAGCACTGCACG[A/T]AACAAATTTGTATGG | 9690 |
rs538171479 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267504 | ACTGATTGGAGCAGG[C/T]ACATTTTGTGTACTT | 9690 |
rs538180792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157168901 | TAATATATTAAATGC[A/G]TATTTAGTGGGTGTT | 9690 |
rs538187268 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156984 | TCAGTTATAAGAGTC[G/T]TCATCATTAGACTTT | 9690 |
rs538188375 | snp | A/G | 4.37704e-05 | 0.00467796 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186979 | TGGCCTCCGTCTGCC[A/G]CACGCTGATGGTGCA | 9690 |
rs538192435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157164186 | TTTTTAAGATACTGA[A/G]TCTTGCTCTGTGACC | 9690 |
rs538197338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157051 | GCGGTAGGAGGAAAA[A/C]ATAAAGGTGTAGGCA | 9690 |
rs538209737 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213658 | AAATGGATCCAGTCA[A/G]ATTTTCATGTTTATA | 9690 |
rs538233633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263336 | GCATACAGAGAATCC[A/G]TGCCCTTTTGTGCCG | 9690 |
rs538237382 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157180587 | TGTGCTACCAAATAC[A/G]CTTGTATATGATGAG | 9690 |
rs538237787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247035 | AGCTGGGATTATAGG[C/T]ATATGCCACCACACG | 9690 |
rs538279619 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256306 | CGCCACAACATCCAG[C/T]GAATTTTTGTACATT | 9690 |
rs538304881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157225159 | AGGCATGAGCCAATG[G/T]GCCTGGCCGGATTTT | 9690 |
rs538322692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189155 | TGAAAGTGAACACTC[A/G]TGTCTGAATATGCCG | 9690 |
rs538367519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157150667 | CATTAATTTATTAAC[A/G]TACTTGTATTTATGA | 9690 |
rs538369594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236461 | TTGTATAACTTTGGC[A/G]TGGTTTATAATTTTT | 9690 |
rs538386879 | snp | C/G/T | 0.00796202 | 0.0626708 | intron-variant | UBE3C | GRCh38.p7 | 7:157231920 | ACCACACTCTTTGGG[C/G/T]GGGGAGGGAGGCTTA | 9690 |
rs538394745 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268890 | TGTGGGAGCAGAGTG[A/G]CCCTTTGCTGATGCT | 9690 |
rs538419416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188537 | ACTTGCTTTTATTGT[C/T]GCACAACCCATTGCT | 9690 |
rs538422026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264252 | TTACACACACACACA[C/T]ACACACCTGGTACTA | 9690 |
rs538439265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252892 | AGGAATGCAGTTGGG[C/G]TGTTTTTGTTGTTTT | 9690 |
rs538459053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264767 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGTCAGG | 9690 |
rs538483268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152367 | TTAGAGATGCGTGGG[A/G]GGCAGTTTGGGTGTT | 9690 |
rs538483426 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252112 | CTGCACTCCAGTGTG[G/T]GTGACAGAGTGAGAC | 9690 |
rs538486915 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192229 | CGGGAAATATGAGTA[C/T]ACTTGGAAGAAGCAT | 9690 |
rs538500122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258660 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 9690 |
rs538519131 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190905 | GCCTCCATGGTGTTT[C/T]GTGCCCCTTTCCTTT | 9690 |
rs538519375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152058 | TTTACATATTAACAT[C/T]ACTGTCACCAGTTAG | 9690 |
rs538527196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237727 | TATCTTTGGCTCTTA[C/T]TTGTGCAATAAAGAC | 9690 |
rs538547793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157629 | CAAGGATATCCACTG[C/T]AGTTTTATTTGAATT | 9690 |
rs538620620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187559 | GCTAATTTTTTGTTT[G/T]TGTGTGTGTGTGTGT | 9690 |
rs538693398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192975 | ATGTTTTTTGAATCT[A/G]TAAATCTTTTAATTA | 9690 |
rs538714181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200748 | CTATCGATTCTCCTA[C/T]CTCAACCTCATGAGT | 9690 |
rs538735636 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236173 | TGATTGCATTTTGTC[G/T]CCTGTAAGTCAGGCT | 9690 |
rs538772582 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254809 | CTTTGGGAGGCCGGG[A/G]CAGGTGGATCACTTG | 9690 |
rs538803487 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157171073 | CCTCCCTGGCCTCTC[A/T]AAGTGCTGGAATTAT | 9690 |
rs538830565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182788 | AGAGTCTCGCTCTGT[C/T]ACTAGGCTGGAGTGC | 9690 |
rs538833418 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157206677 | CATGGCAACCTCTGC[C/T]TCCTGGGCTCAAGCC | 9690 |
rs538839806 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157188812 | CAATTTTGATTTTTT[A/T]AAAAAAGTATTTGAA | 9690 |
rs538840927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259353 | CCCATTTTCAAGGGG[C/T]GCAGGCAAGTTATCT | 9690 |
rs538852412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182469 | CTGGAGGGATGTGGT[C/T]TGGGCAGTGTGTTCC | 9690 |
rs538866245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189127 | AAACTTGGAAGCATA[C/T]ACAAGAAACTCATGA | 9690 |
rs538897998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219832 | TGAACCTGGGAGGCA[A/G]AGGTTGCAGTGAGCC | 9690 |
rs538939031 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194539 | TAGGCAGTAGGTCGA[-/G]GCTGGAAGAATTCTG | 9690 |
rs538945601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157219410 | GAGATGGGGCCTCTC[A/G]GTGATCGAGCATCCC | 9690 |
rs538949174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157152832 | ACCACATCCTGCAGG[C/T]ACTGAGAAGGTGGTT | 9690 |
rs538963269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157250236 | GTTGTATTGTTTTGA[A/G]ACGGGGTTTCACTCT | 9690 |
rs538967194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181095 | AATATGTGGTCCTTA[C/T]TGAGCTCCTTCCTGA | 9690 |
rs538985298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158289 | TCATGGACTGGCCGA[A/G]AGAGGGAACCTATTC | 9690 |
rs538989366 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192498 | ATCAGCAAAGACTGA[C/T]CTTTGCTGGCAAGCA | 9690 |
rs538990752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157188732 | TATGGCTTAAACATA[C/T]TAGGTTCTAGTATTT | 9690 |
rs538995473 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157247024 | GCCTCCCAAGTAGCT[A/C/G]GGATTATAGGCATAT | 9690 |
rs538996298 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157228144 | TGCTTTACGATGCTC[A/G]TTGTCTTATCTCCGA | 9690 |
rs539005652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194631 | TTAATGCTAGGGAGG[C/G]CTTGAAGGAAGAAAG | 9690 |
rs539008286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157195232 | AAGATATGTGAGGAG[C/T]CTCCTGTGTAAATGA | 9690 |
rs539010496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264906 | TTTTAGCTGTATCTT[A/G]TGTTCAGTTTTCTAG | 9690 |
rs539020688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160913 | GCGTGTTTGTGCGTA[G/T]AATCCTATGGATTAA | 9690 |
rs539030708 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157201994 | CTTAACAGTTACTTA[C/T]CTGTATATATTATAG | 9690 |
rs539042798 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157201185 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT | 9690 |
rs539078147 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157196751 | AGGTGGGTGGATCAC[C/G]TGAGGTCGGGAGTTT | 9690 |
rs539105052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157242865 | TTCTAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 9690 |
rs539124766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157249608 | GTGAGCCACCGTGGC[C/T]GGCACGACAGAGCCT | 9690 |
rs539127117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210674 | TTGTGCCAAATTTGA[A/G]TTGAAGAATTCGAGG | 9690 |
rs539162978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244292 | GAGTTTAGAGTTAGT[A/T]ACACAAGCCCCTAGT | 9690 |
rs539166985 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262710 | ACAGGCATGAGCCAC[A/C]GCGCCCATCCTCTTC | 9690 |
rs539174963 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240350 | GTGAGCCATAGCACC[C/T]GGCCAGCAAGCTGTG | 9690 |
rs539179055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166665 | GAATTGCTTGAACTC[A/G]GGAGGCGGAGGTTGT | 9690 |
rs539190836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149346 | CAGGCGTGAGCCACT[A/G]TGCCTGGCCAGGAAT | 9690 |
rs539195774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153656 | ATTATCACGAATCTT[C/T]CTTGCTCTAAGAATG | 9690 |
rs539200491 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157265406 | GAAGGTGGAGTCACC[A/C/G]GTTCTTCGTGGCCAT | 9690 |
rs539211197 | in-del | -/AGTT | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157244479 | ATTATCTGCTTGCTC[-/AGTT]AGGATGGCTTTAAAG | 9690 |
rs539236383 | in-del | -/TTTTTTTTTTTTTTTTTTTT | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157208056 | TTTAATTTGCAAGAC[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 9690 |
rs539239456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185383 | CTCTATATTCTTTTT[C/T]AATACATAAGGGTTT | 9690 |
rs539264710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140605 | CTTGCTTACAAGTTC[A/G]GAAGGTGAGCTGCAG | 9690 |
rs539265447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191430 | TTGAGTAGCTGGGAC[A/G]ATAGGCGTGCCACCA | 9690 |
rs539268648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227253 | GCAGTTCTGGAGCAG[C/T]ACCTGTAGGGGAGGA | 9690 |
rs539286227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146621 | ATTACTGTAACAGAT[C/G]TGTAGTAAACTGTAC | 9690 |
rs539303887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229655 | TATTTTAGAGATGGG[A/G]GTCTCACTTTCAGCC | 9690 |
rs539315087 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172236 | AGTCAGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 9690 |
rs539362908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238329 | GTGGGCCTCCTTGGC[C/T]TTGGTGTAAGTAGCT | 9690 |
rs539444297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157212368 | TTTGGTTGCAATACT[A/G]TATCTAAATATCCGT | 9690 |
rs539479417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239844 | CAAGAAGAGGTAGAG[A/G]AACACTGGGTGCAGC | 9690 |
rs539482859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211734 | AGGTTAGAGTGTTTT[A/T]TTCTCAGTTATTTGA | 9690 |
rs539486009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244002 | TTTGGGAGGCCGAGG[C/T]GGGTGATCACCTGAG | 9690 |
rs539486189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202895 | TGGTCTTGTTTTCTT[C/T]TTAGGAACAAGAAGT | 9690 |
rs539503162 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138213 | ACATTTTCAACTTAC[A/C]ATATTTTCATCTTAC | 9690 |
rs539514119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160373 | AGCCCCTGCAGCAGC[C/T]ACTTTCAAATTTAAC | 9690 |
rs539519856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217977 | GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTGC | 9690 |
rs539524567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210034 | AGATACAAAAAATTA[C/G]CTGGGCGTGATGTAC | 9690 |
rs539542143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239436 | CTGATGCTCCTGGGA[A/G]GGTAACACTGGAAGG | 9690 |
rs539562992 | snp | A/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137444 | GCTAATTTTTGTACT[A/T]TTAGTAGAGACGGGG | 9690 |
rs539603719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156414 | CAGGTTCAAGTGATT[C/G]TTGTGCCTCAGCCTT | 9690 |
rs539640521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184696 | TACTTGAGAGGGTCT[A/C]AGGGCTTCCAGGTGA | 9690 |
rs539648514 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207169 | GTTGGTACAGGTAGC[A/G]GAAACCTTAGTGAAG | 9690 |
rs539657722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261972 | TACTTTTAAGTCTCC[A/G]AGTAGGAAATTCAAT | 9690 |
rs539667971 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157224646 | TTCTAAAGATTACTT[-/G]GGTTCCGTTCTTCAG | 9690 |
rs539675602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157199188 | TTTTTTAAAAACTCA[A/G]TTTCTCAACTGAAGA | 9690 |
rs539676628 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266483 | TCATCGTGGAGATCC[A/G]CTTCTCGTGAGTCAT | 9690 |
rs539688889 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157149712 | AAAATAGATGGTCTC[A/C]TAAGACCATAGAATA | 9690 |
rs539698202 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204355 | CTGAGACGAGATTGC[A/G]CCATTGCACTCCAGC | 9690 |
rs539709042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246084 | AGATGTTTGCTTTTG[A/G]GAAAACCTCAACAGC | 9690 |
rs539711187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205405 | ATAACTGATGATGTG[C/T]TGGTGGTGATGATTC | 9690 |
rs539727627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157149215 | GTGCCTGCCACCACA[C/G]CCAGCTAATTTTTCT | 9690 |
rs539733648 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230754 | GTATCTGTATTGGGC[C/T]GCATTCAAAGCCATC | 9690 |
rs539746861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240738 | GAGAGGAGACCTGTG[A/G]AGTCGAGGTCCTTCA | 9690 |
rs539812244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157167639 | ACCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 9690 |
rs539813278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250636 | CCAAGAGCCATATTT[A/G]TTTGGTTACAACTTA | 9690 |
rs539817214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204818 | GTGTTGGCTGTTTGA[C/T]AAATAATCTCAAAAC | 9690 |
rs539818624 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157177946 | TTTTTTTTTTTTTTA[A/T]GAAAAAGGAAAAACA | 9690 |
rs539836535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257275 | TAGTTACACATTGTG[G/T]TTATGATTGCCTGTG | 9690 |
rs539847558 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139955 | ATTTGCCACCAGCCT[C/T]CTGGAAACTGTGGAG | 9690 |
rs539858129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157184205 | GAAAGTCTCTCCCAC[C/T]GCTTTGTTAGCACGT | 9690 |
rs539865622 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138630 | GCCCCGCACCCAACA[C/G]CTCCCGCGCCCCTCG | 9690 |
rs539897603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256746 | GCTCTAGAGATCATG[A/G]AAGTGCACAGCACGT | 9690 |
rs539927471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148538 | TTTGTAAAACTGCCC[C/T]CTATTATATAATTGA | 9690 |
rs539939209 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180545 | GACTGTTTCAAAAAC[C/T]AGCCCATGCAGATGG | 9690 |
rs539940100 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137612 | CTGTGTCGCCCAGGC[C/T]GGAGTGCAATAACAC | 9690 |
rs539947005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143330 | CAGAAATGGACTAAA[A/G]CTAGCTTAGTAGGCA | 9690 |
rs540025724 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268442 | CATTGTCCTATTTCT[A/G]TCTCCACTTTGTGCC | 9690 |
rs540053829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205910 | TCAGAAGCTCCAGGT[A/G]GCTCAGCCAAGCTCC | 9690 |
rs540084946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211238 | TTAGTGGTTAAGTTG[C/T]ATTTTTTCAGTTCCA | 9690 |
rs540135057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217728 | TGTAATCCCAGCTAC[A/T]CGGGAGGCTAAGGCA | 9690 |
rs540147381 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263729 | AGCGCTGTTGGCACC[A/G]AAAGCACTTTTTTTA | 9690 |
rs540172644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168074 | AAAGTCCTGCTAGCC[A/G]GGCACGGTGGCTCAT | 9690 |
rs540173596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157223690 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCGA | 9690 |
rs540180759 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142756 | CTGTGCTCACTCCCC[A/G]GGTAATGGGATCATT | 9690 |
rs540180998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223093 | GATCCTGCACTGTGC[A/G]TGGCTCATGGGTCTG | 9690 |
rs540190811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157229342 | TTTTTGAAATGGAAC[C/T]TCTCTCTTGTTGCCC | 9690 |
rs540209971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256352 | TTCACCATGTTGGCC[A/G]GGCTGCTCTCGAACT | 9690 |
rs540221695 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154306 | GCCTGGTGACAGTTC[A/G]AGATTCTGTCTAAAA | 9690 |
rs540244638 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157191071 | TGTTATAATTTGCCC[A/G]TAGTTTCATTTAAAT | 9690 |
rs540267397 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157192123 | CATCAAATAAATAAA[A/T]TAGACTTGCCTTCGT | 9690 |
rs540268327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157142554 | GGTGGAAGACGAGAA[A/G]GCATTCCAGGTTCGT | 9690 |
rs540282665 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222393 | ATGATGTCTAAGATA[A/C]CTTCACCTAACACTT | 9690 |
rs540323713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228708 | CACTGCATCCCTGCT[A/G]CTGTGCAGAGTGGCC | 9690 |
rs540336317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157190046 | CCTCAGGTGATCTCC[C/T]GCCTCAGCTTTCCAA | 9690 |
rs540339011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157211820 | AAATGAATTCACACA[A/G]GGTGCCTGTTCCTGC | 9690 |
rs540339270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204207 | ATAAAGTTTAAAATG[A/T]AATAACTGATTTTCT | 9690 |
rs540359439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234364 | AGATTGTATGAGTTA[A/G]GCATCCTCATATTCT | 9690 |
rs540373125 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157174475 | TTTTTGGAGACAGGG[-/TC]TCTCTCTCTCTCGCC | 9690 |
rs540403422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157256831 | TGGACTTTAGTTTCC[A/G]TGGGTGTCTGGACCA | 9690 |
rs540414766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157250018 | AAATTTGGGGGGAAA[A/G]AATACAAATCCAAAC | 9690 |
rs540433243 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166933 | GTGGTGGTGGTGGTG[A/G]TGGTGGTGGTTTTTG | 9690 |
rs540443230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263195 | TCAGCTTAGTCTGCC[C/T]ACCGTAGCCGCTATG | 9690 |
rs540450820 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265958 | ACAAGCAAGCCACTT[G/T]TCATCATGCATTTGG | 9690 |
rs540454015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244824 | ACAGACAGTTGAAAA[A/G]TTCGTTACAGGTCTT | 9690 |
rs540462118 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243573 | CACGGCCTGGCCCCT[C/T]CCAGGGAGCTTGGTG | 9690 |
rs540477820 | in-del | -/AAG | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157161039 | AGATAAGAACTCTAT[-/AAG]ATTGGAGGAAGATTA | 9690 |
rs540494896 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137781 | GTTGGCCAGGCTGGT[C/G]TCGAACTTTTCACTT | 9690 |
rs540547608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143719 | TAGATTCTTCAAGAA[G/T]CGGGGAGTGGTCGTT | 9690 |
rs540584599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155977 | TCTACATCTGCATAA[C/T]TTGAAAGATAAGGAT | 9690 |
rs540585798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150055 | CACTGGGCACAACCT[A/G]CCTAGGGTTGGTTAT | 9690 |
rs540593388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238133 | GATTTAGCAAATGTA[A/C]CTTTATGAAATAAAA | 9690 |
rs540639522 | in-del | -/CATATAAA | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157205581 | GCCTTTTTTATCCTC[-/CATATAAA]CAACCTTTTTGTGTC | 9690 |
rs540656243 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157240774 | TCAGTGTAGCGGTGG[G/T]TAGAGCTAAGATCAG | 9690 |
rs540665279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157202096 | GGAAATTGCTTTGCT[C/T]CATATGACTTTACTC | 9690 |
rs540689857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245725 | GAGGGGATGTTATGC[C/T]GGCTCTAGTTATCAG | 9690 |
rs540698913 | snp | C/G | 3.35323e-05 | 0.00409451 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207888 | ACTAGCTCTGAAATG[C/G]AACAATGCATACAGA | 9690 |
rs540701684 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243019 | AAGATTGTGCCACTG[C/G/T]TCTCCAGCCTGGGTG | 9690 |
rs540718188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162327 | AGCCTCTCGAGTAGC[C/T]GGGACTACTGGTATG | 9690 |
rs540718754 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174072 | TAGCTACACTTAAGA[A/G]GCTATCTTTGCCGAG | 9690 |
rs540726504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228890 | CAAAATTACTGACAC[A/G]TGTACATAGCAATCT | 9690 |
rs540727266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242031 | GCTGAGGGATGTGGA[C/G]TTTCTTTTTAGAATA | 9690 |
rs540739998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214980 | AGTCAAGGGTCAAGG[A/T]ATAGCTGACTCCAGT | 9690 |
rs540742615 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154556 | TATTTTTCATGGTAT[A/G]TAATACTCCATAGCA | 9690 |
rs540756787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157161547 | GCCTCAGCCTCCCCA[A/G]TTCAAGTGATCTTTC | 9690 |
rs540785318 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157227433 | GCGTGGCGCAGTGGC[C/T]CACGCCTGTAATCCC | 9690 |
rs540793128 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177759 | GAGACAGAAGGCAGC[C/G]TGCGGTAAGCGGATA | 9690 |
rs540807995 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157180059 | ATATTTAAGAAATAT[A/G]CATTATTTGAAATGT | 9690 |
rs540871786 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165860 | GTAATTGGATCTTCC[A/G]TGGGGTTTGTTTCTA | 9690 |
rs540874902 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175988 | AAATAAAGGAATCAT[A/G]CTTCACTCAACAGCC | 9690 |
rs540924636 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267899 | TTCCTCCCTCCCTTC[C/T]TTTTTTAAATGATTT | 9690 |
rs540927670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195521 | TTTTGTAAATTGATG[G/T]TGCTGATGGCTCCTT | 9690 |
rs540952428 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195817 | AGCACCTATGAGTGA[C/T]GTAAATTTATTTGTG | 9690 |
rs540956968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232439 | TCTCTGCTCACTGCA[A/G]ACTCCACCTCTCAGG | 9690 |
rs540974134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158531 | GCCAAAGCTGTGATT[A/G]AAAGTGATGATTAGT | 9690 |
rs540984393 | snp | A/G | 0.0002318 | 0.0107632 | intron-variant | UBE3C | GRCh38.p7 | 7:157256873 | TCCTGAAGGGTGGGT[A/G]TGCTTTGCATTTCAT | 9690 |
rs541003499 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157265244 | GCTAGGTCTCTGAAA[C/T]CCGTGCCAGATACTA | 9690 |
rs541019121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195060 | AGAGAAAGTGATGAA[A/G]GTATGGCTGTATAAC | 9690 |
rs541046574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248817 | CGGCAGCCCCTCCTG[C/T]GGAGCTCCACTCTCG | 9690 |
rs541072798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177388 | CCCGTCCAAGGCTGT[C/G]CCGATAAACCTGGAG | 9690 |
rs541095144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259754 | TCGGAGAAGTGGAGC[A/G]ACCCAAAACCGGATT | 9690 |
rs541105841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153953 | AGTGAGCCAAGACCG[C/T]GCCACTGCACTCCAG | 9690 |
rs541115596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157216538 | TAGATCCCAGTGTCT[A/G]TTCTTTCCTTCTTTG | 9690 |
rs541126807 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236783 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGTGCGATC | 9690 |
rs541129221 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141587 | TCTGTGCATCCAAAC[A/G/T]TAGATACAGTAAAAA | 9690 |
rs541146845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227775 | AACAAGCCTCAAATT[C/T]CCTAATGAATCCTTA | 9690 |
rs541150263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222141 | CTCCCAAAGTACTAC[A/G]ATTACAGGTGTGAGC | 9690 |
rs541153780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157164573 | TATTGTTTATCCTAC[A/G]TTATATCTTGTGATA | 9690 |
rs541163657 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235478 | AGAAGCTAATAGTTA[C/T]GTAAGTCTGGTGAGG | 9690 |
rs541179814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160557 | TTGATTGTATCATTT[G/T]TATGGTACCAAGTAG | 9690 |
rs541190610 | in-del | -/AC | 0.0260105 | 0.111035 | intron-variant | UBE3C | GRCh38.p7 | 7:157264357 | CATGCTCGGCCTGTT[-/AC]ACACACACACCTGGT | 9690 |
rs541194711 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157265581 | AGTGCCCAGCAACAC[A/G]TCGTGCCGCGCGTGT | 9690 |
rs541215672 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157260250 | GAAGCCTGAATGTTA[C/T]AACAGTGAGTGCGGA | 9690 |
rs541235813 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224234 | GGAGTGTCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9690 |
rs541245289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157182683 | TGTTTGAAAACATAC[A/G]TACATACATACATGC | 9690 |
rs541280328 | snp | A/G | 0.000202614 | 0.0100631 | intron-variant | UBE3C | GRCh38.p7 | 7:157188948 | TAACACTGATTGTCA[A/G]GGTGTACAAATGAAT | 9690 |
rs541285948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249014 | TACTTTTGTTACTTA[C/T]ATCCTTTTTAAAAAA | 9690 |
rs541323366 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240635 | TTGCAAGTTCAGAGT[G/T]GTTACAAGAGCCTGC | 9690 |
rs541323425 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220673 | GGGAGTTCTGAACCA[C/G]GATTGCCCCCGACAG | 9690 |
rs541348999 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160909 | TGATGCGTGTTTGTG[C/T]GTATAATCCTATGGA | 9690 |
rs541408197 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157237631 | ATTGAGACCATTCTG[-/T]TTTTTTCTGGGCCAT | 9690 |
rs541414496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196170 | CAAGCCAAGGAATGC[A/G]GATGTTCTCTAGAAG | 9690 |
rs541527006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201618 | TTTGCTAAATTGTAC[A/G]TTGATCTTCAGTGTA | 9690 |
rs541557535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176945 | CTGCCACGTGCCAGA[A/G]CATTGAATTTTTCTT | 9690 |
rs541560917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208706 | TTTTAACATATCTTC[A/G]TTCTTAACCAGAAAG | 9690 |
rs541569559 | in-del | -/AAAAG | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157235198 | TGTCTCAAATTAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 9690 |
rs541591617 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238020 | TGGCACCACCACACT[C/G]CAGCCTGGGTGACAG | 9690 |
rs541609178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239180 | TGGTAACACTGTATA[A/G]CCCCTAAACTGGAAA | 9690 |
rs541646063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157196254 | ATGTTAAAAGCACCG[C/T]GAAACCCGTTTGGAC | 9690 |
rs541707339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154105 | GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGTTCA | 9690 |
rs541710052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265166 | GGTGAAGCCCCTGCT[C/G]CTGCTGCCAGGCCCA | 9690 |
rs541711921 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157227878 | AAAGATTTGGAAGAA[G/T]CTTCTCATATTGTTT | 9690 |
rs541721176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202589 | TTAAACCTGGAAGGC[A/G]GAGGTTGCAGTGAGT | 9690 |
rs541726693 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261473 | TTTTCTCAATGTTCT[A/G]ACATATGTGAAATTT | 9690 |
rs541736298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157147822 | CCTTCTGCAGCTTGT[A/G]GATATGATGGATCAC | 9690 |
rs541756114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209625 | TCTTTGTTAATAAAG[C/T]TTTCCATGATGTGCA | 9690 |
rs541774001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233043 | TAGGTAGTCACTCCC[A/T]ATCCTGCCCTTCCTC | 9690 |
rs541787067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233539 | CCTGCCTCAACCTCT[C/T]AAAAGGCTAGAATTA | 9690 |
rs541799165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153317 | GCCACTGTGAAACCC[C/G]TTTACTGCAAAAGAC | 9690 |
rs541817500 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198014 | GTCCTCCATATCCCA[A/G]TTCACTTGGCCACCA | 9690 |
rs541844374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249220 | TCGGTCTACAGAGCA[A/G]CCGTGCACCCATTAG | 9690 |
rs541853912 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220110 | CAGCTACTCAGGAGG[C/G]TGAGGTGGGAGGATC | 9690 |
rs541873938 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268739 | GTGCTGCTCTGACTC[A/G]AAGACGGGACAGTCC | 9690 |
rs541879697 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137056 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 9690 |
rs541889602 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240666 | CTTTGAATCTAGGCT[C/G]TTTAGAGAGGAAATT | 9690 |
rs541933021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222928 | CAGGGCACCGCCCAC[C/T]GCTGGATCTGGCTGC | 9690 |
rs541939813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159146 | AAGTCTCTCTCTCCT[C/T]GACTGTTATCTCAAG | 9690 |
rs541940288 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157217226 | TTATATTAAAGCCTT[A/C]ATGATTCTTTGTGAG | 9690 |
rs541941858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157218487 | GTCACAGAAATATTC[A/G]AGGAGAGAAAACAGG | 9690 |
rs541952567 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261786 | TAAATGTGATTGTTA[C/T]AGACAAAAAATCATT | 9690 |
rs542022085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234986 | CACCTGAGGTCGGGA[A/G]CTCGAGACCAGCCTG | 9690 |
rs542023241 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157255098 | GCACTCCAGCCTGGG[C/G]GACAGGAGTGAAACC | 9690 |
rs542024003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260321 | CAGGAAAACGCTGCC[A/G]CCTACAAGCAACACA | 9690 |
rs542024840 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157267387 | AGATGGCGCCATTGC[A/C]CTCCAGCCTGGGCGA | 9690 |
rs542047018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191206 | TGTGATTTAGATAAA[C/T]AGCGGTGCGCCTCGA | 9690 |
rs542062447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260804 | CTAATCATGTGAGTA[A/G]CAATAAAAATTCGAA | 9690 |
rs542080075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239652 | AGAAAACTTGAGCAG[C/T]CGCTTAAGGGATATG | 9690 |
rs542102955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141422 | GGTTGTTGTGGGACC[A/G]TCCTAGAGTGCACTT | 9690 |
rs542107626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183115 | ATGTGGGGTTTTTTT[C/T]CCCACACACCAAGCA | 9690 |
rs542108699 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200896 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 9690 |
rs542187234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265886 | CACATCTGAAAAACA[A/G]TATTCAAATTTCCCT | 9690 |
rs542188200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160627 | GATGTCTTAGTTGGT[A/G]TCTGCAAAATTTCTC | 9690 |
rs542246268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172515 | ATTATTCCTCTAGTG[A/T]TTGGCTTTAAAACCC | 9690 |
rs542261297 | snp | A/C/G | 0.00398691 | 0.0444912 | intron-variant | UBE3C | GRCh38.p7 | 7:157248832 | CGGAGCTCCACTCTC[A/C/G]AGGCTGCGGCCCAGG | 9690 |
rs542277027 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157139451 | CGAGACTTGGGGCTG[A/G]ATTCGGGGCCTCCCT | 9690 |
rs542289858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157209667 | TGTGTATGATATCAG[A/G]TAATTTCACTGTTTT | 9690 |
rs542334229 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142689 | CACCAGGGACTACTA[C/G]AGGGGGAAAGAGAGG | 9690 |
rs542338423 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157138990 | AGGTGCAAGCGCCGG[G/T]TTTGCTGCCCGCTGG | 9690 |
rs542360750 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211639 | GCATAAATGGGTTAA[C/T]AAGTGGTAACTAAGG | 9690 |
rs542363878 | snp | A/C | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269697 | TTTTCTACGTTCTGT[A/C]CTACTTTCTGCTTTC | 9690 |
rs542384750 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202605 | GAGGTTGCAGTGAGT[C/T]GAGATCATGCCACTG | 9690 |
rs542389262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157172035 | TATTTATCTTTTTTT[C/T]TTTTCCTTTTTGAGA | 9690 |
rs542391098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177809 | ACCCAGAACCCTGCA[C/T]GTTATTCCCCTCCTG | 9690 |
rs542412972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151755 | AGAGGGGGCTATGCA[A/G]TTGGACCAAGAGGAG | 9690 |
rs542422486 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214172 | TGTTATATTGGTAAC[-/AT]GTGATTACTTCTTTT | 9690 |
rs542460178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236921 | ATTTTTAGTAGAGAC[A/G]GGGTTTCATCATGTT | 9690 |
rs542470713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197632 | GTAACACAGTGTTAA[A/G]AATATCTGCTTCTAG | 9690 |
rs542475264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247191 | GCACCTGGCCTGACT[A/G]GATATATTCTAACAC | 9690 |
rs542502605 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226549 | GTGATGAGTTGTCCA[A/C]TGTGAAATGACAATT | 9690 |
rs542506146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157275 | ACTGAATTCTTAAGC[A/G]AGAAATTTGACTACA | 9690 |
rs542506284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164368 | TGCTTTGCTGCCGAG[A/G]CTGATTTCAAACTAT | 9690 |
rs542517284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241490 | ATCACTAGTCATCAA[A/G]GAAGGGCAAAGCATA | 9690 |
rs542544781 | snp | A/T | 0.000199684 | 0.0099901 | intron-variant | UBE3C | GRCh38.p7 | 7:157163767 | TGGGAGTTTTAAAAT[A/T]GAAATTATAACCTTA | 9690 |
rs542625355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181788 | GGTTTTTACTTTATT[A/G]GTGTTGATTTAGTTT | 9690 |
rs542646391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213427 | GGGCTTGTCTTAGTG[C/T]TCCAGGTGATTCTAA | 9690 |
rs542669095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157188768 | GAGCAAGTAGGCTTA[C/T]TCTAACTGTTACAGA | 9690 |
rs542695807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145964 | GGATCTTGCTTCTCG[C/T]GTTGTGTCTAAAAAG | 9690 |
rs542746028 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | UBE3C | GRCh38.p7 | 7:157264552 | GGTATTACAGGTGTG[A/C]GCCAACATGCTCAGC | 9690 |
rs542746961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232166 | TTTTTTAATAAGGAC[A/G]CCTGTCATTGTATTG | 9690 |
rs542756541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258315 | CATGTAGTCCCAGCT[A/C]CTCTTGAGGCTGAGG | 9690 |
rs542761550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197080 | AGTAATATATCTAAA[C/T]CAGTAAGTAAAAAGG | 9690 |
rs542792987 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157178401 | ATACTTCTTACAGTG[-/T]TTTTGTAATCTTTAA | 9690 |
rs542818407 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157171101 | TATAGGCGTGAGCCA[C/G]TGTACATGATTTAGG | 9690 |
rs542851872 | snp | C/T | 4.65918e-05 | 0.00482636 | intron-variant | UBE3C | GRCh38.p7 | 7:157207948 | AAGGTATAGAGTATA[C/T]GTATTTTTTTGTTTA | 9690 |
rs542883712 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157257346 | AATGTCTCATAAATC[A/T]GTAACACATCTTGGG | 9690 |
rs542891783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215559 | GTATATATATAATAG[A/G]TATATATTAGAAATG | 9690 |
rs542908622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157206867 | GTGAATAAAGTGGAC[A/G]GTGGGAGCAAGGCCA | 9690 |
rs542998807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226631 | GATTTCTAATAATTT[G/T]TATTGCTTACATAAA | 9690 |
rs543058900 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157188153 | TCTGCTAGGACCCAA[A/G]GGACTGATGTTGCAT | 9690 |
rs543078644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140212 | TTCTTTAAAATGCTT[C/T]ACCTAGTTTTTCTTG | 9690 |
rs543102598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246943 | TTGCCCAGACTGGAG[C/T]GCAGTGGCACAATCT | 9690 |
rs543122322 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157152213 | AGGGACAGAGCTGGG[A/G]GGAAGGTAGTCAGGG | 9690 |
rs543137035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226138 | TTGTTCTAAAAATCT[C/T]GATGGTAGCCATTTA | 9690 |
rs543171185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145412 | AATTGCAGCTACTCA[C/G]GAGGCTGAGGCAGGA | 9690 |
rs543172371 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232707 | TATTGTGATTAATTT[C/G]TGTAAGAATCAGAGC | 9690 |
rs543207469 | snp | A/G | 3.31257e-05 | 0.00406962 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170370 | GGGGGCGCTTTTCCC[A/G]TTGCTAATGGCCCCA | 9690 |
rs543269358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248076 | CTGTTGAGGAGGAGC[A/G]TTTGTTGGCTTCTGT | 9690 |
rs543276697 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157242562 | CTGTCTTTCAGAAGC[A/C]GGAGTGTAAAACTGT | 9690 |
rs543284615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157188202 | AGTAAGCAGGTCTGA[C/T]GTTAATTCACGTTAC | 9690 |
rs543299887 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255552 | TTAAGGAAATGAAAT[C/T]AGTCTGACCTTTCCT | 9690 |
rs543305310 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191534 | GGGCCCAAGTAATCT[G/T]CTTGTCTCAGCCCTC | 9690 |
rs543309352 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157152222 | GCTGGGAGGAAGGTA[A/G]TCAGGGAGAGAGCTG | 9690 |
rs543318918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201372 | AACAATAGTAATTAT[A/G]ATATTGTGATATATT | 9690 |
rs543319723 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173127 | GCCTGTAATACCAAC[A/G]CTTTGTGGGGCTGAG | 9690 |
rs543348270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237433 | GCGACAGAGCGAGAC[A/T]CCGTCTCAAAAAAAA | 9690 |
rs543348898 | in-del | -/GAATGG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157228760 | CGACCACTGCTCAGT[-/GAATGG]GAACTTGGTATTTCT | 9690 |
rs543352817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253755 | AAGACAGAGTAAGGT[G/T]CTGGGCTTCGGAGAC | 9690 |
rs543365130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140713 | GCGCGGCCTCTGTTG[C/G]AGGCAGGAACACCCC | 9690 |
rs543387250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259740 | TGGCAGCGGGAGCTT[C/T]GGAGAAGTGGAGCGA | 9690 |
rs543395126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170655 | AAAAATGTGTATCCA[A/G]AAATAGGCTTTTTCG | 9690 |
rs543430105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254468 | AGTGGCGCGATCCCA[C/G]CTCACTGAAACCTTT | 9690 |
rs543431880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157176307 | GAGATAAGAGTCTTG[C/T]TCTGTCACCCAGGCT | 9690 |
rs543433876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176918 | TGTATGTTAGTAAGT[C/T]GACAGTCTTATCTGC | 9690 |
rs543445579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207089 | TGAATAGTGGCCTTA[C/T]TAGAGCTCTTCTTAG | 9690 |
rs543453207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157169745 | GGAGTGCAGTTGCAC[A/G]ATCTTGGCTCACTGC | 9690 |
rs543482296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141380 | CATATGTGACTTAAA[A/G]AGGGGGACGCTGTCA | 9690 |
rs543483735 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157214301 | AACTTAATTGTCTCA[C/T]ATAATTTGATAATGT | 9690 |
rs543486007 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142898 | CGCTCACGCTGGAGC[A/G]CAGTGTTGCCCAGGC | 9690 |
rs543491423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175731 | CTGGACCAAAGGTAG[A/G]AATAAAGAACCTATT | 9690 |
rs543529684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146227 | AAAGATCAGTTGGCT[A/G]TATTTTTATGGATCT | 9690 |
rs543534508 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157237298 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 9690 |
rs543537322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227364 | CTTCAGCCAGAGTAG[A/G]ATGCGTTTCTTACTT | 9690 |
rs543539790 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252896 | ATGCAGTTGGGGTGT[C/T]TTTGTTGTTTTTTTG | 9690 |
rs543552737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259417 | ACCGTTGGGAGTGTA[C/T]AGATGGCAACATATT | 9690 |
rs543565528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232365 | TAGTTTGTTTGTTTG[C/T]TTGTTTGAGACGGAG | 9690 |
rs543572556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253130 | ATATTGTATTTTGCT[C/T]GTGTACTGTTTTGTA | 9690 |
rs543579202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166174 | TGTCATGAATGCTTT[C/G]CTCATTCTTTTTTCT | 9690 |
rs543592352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265518 | TTTGCACAACTGTGA[A/G]AACCAGGTACGTATT | 9690 |
rs543594597 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157247031 | AGTAGCTGGGATTAT[-/A]AGGCATATGCCACCA | 9690 |
rs543598373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188878 | CACAGGCCCTCACTG[A/G]TTAATATTAGTCCCT | 9690 |
rs543603826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195640 | TTGTTTTCTAGGTTC[A/G]CAAGTGCACAGATGG | 9690 |
rs543604347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157265095 | CTCTTGTGCATAAAT[C/T]ATCATGTGCATCTCT | 9690 |
rs543682060 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157243554 | GGAGTATTAGAGTGA[A/G]GCCCACGGCCTGGCC | 9690 |
rs543729424 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157214515 | TAAATATGTAAATAT[G/T]TCAGAAAGGATGACC | 9690 |
rs543731694 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157157983 | ATATAGATATATATA[G/T]ATATAGAGAGAGAGA | 9690 |
rs543785546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262097 | CCCCTTCATTCAGAG[A/G]TCCTTTTCTGTTTCA | 9690 |
rs543793226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179163 | CTGCAGTGCAGCTGC[C/T]GGTCCTTCACCTGAC | 9690 |
rs543856883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182589 | TTAAATGGGAAAGCT[A/C]TTCTGTGAGTCAGGC | 9690 |
rs543884052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221508 | AGCACTTTAGGAGGC[C/T]GAGGTGGGCGGATCA | 9690 |
rs543886568 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184799 | TAGTATCGAATGAAA[A/G]AGATCACAGCAATAA | 9690 |
rs543898960 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137853 | ACCGGCGTGAGCGAC[A/C]GTGCTCGGCCGCAGG | 9690 |
rs543916388 | in-del | -/A | 0.159292 | 0.232964 | intron-variant | UBE3C | GRCh38.p7 | 7:157221440 | TTACAGTTGTCATTT[-/A]AAAAAAAAAAAATTC | 9690 |
rs543918928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226803 | TCATCAGCTGAGACC[A/G]AGTAAACTTAGGTCT | 9690 |
rs543933269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157184959 | CCGTTTTTATAGTGG[A/G]CAGTGGATGCTGGAA | 9690 |
rs543944091 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267811 | TCCTTCGTCAGCAGC[A/G]CCTCCCCAGACCCAC | 9690 |
rs543946052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261544 | TGTTAGACATCCAGT[A/T]TGGAAAAATCATCTT | 9690 |
rs543966345 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157142916 | GTGTTGCCCAGGCTG[C/G]AGTGCAATGGTGCGA | 9690 |
rs543969822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159301 | TTTGACACAGCAGGC[A/G]TGTGGGGAAAAAAAG | 9690 |
rs544001653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229484 | CACGCCCGGCTAATT[G/T]TTTTTTGTATTTAGT | 9690 |
rs544004682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238578 | GACTAAGCTGGGAAA[A/G]GTGCGGGCAGGAGCA | 9690 |
rs544007393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157165724 | ACATCCATTGACTTC[A/G]TAATTTCAGTTTTTG | 9690 |
rs544009647 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218655 | CCAGGCTGGGGTTGC[C/T]TCACAGCAAAAGAAG | 9690 |
rs544027329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157202227 | TTTTCTTATTTGAAT[C/T]GTGTAATTTAAAAAA | 9690 |
rs544047048 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157162369 | CCGGCTAATTTTTGT[A/T]TTTTTAGTAGAGACG | 9690 |
rs544064375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208849 | ATTTCTGCAGCAAAC[A/G]CATCTAGTCAGCTAA | 9690 |
rs544087560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157167758 | AACCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 9690 |
rs544093274 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229472 | GGCATGCACCACCAC[C/G]CCCGGCTAATTTTTT | 9690 |
rs544147979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173727 | ATAGTTATTTTACAT[C/G]TTATTTGTTAACTGA | 9690 |
rs544154626 | snp | A/C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138373 | ATGAGGCAAATCTGC[A/C/G]CATGTCTGTGTACAT | 9690 |
rs544159267 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157211905 | GCAAACCACAGAGGC[C/T]GGTCCTGTGGAAGCA | 9690 |
rs544162545 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157194571 | GGCGCATGCCAGAAA[G/T]AAGCCAAATTGCCTT | 9690 |
rs544180106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217757 | CAGGAGAATCACTTG[A/C]ACCTGGGAGACAGAG | 9690 |
rs544219861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185593 | TATGTTTCTGTGTTG[C/G]CTTTTCTTTCCCCTG | 9690 |
rs544244466 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268637 | GTCTCCCATCATCCG[C/T]TCGCCCTCCTTTCCC | 9690 |
rs544246857 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166005 | ATTTGCTTGGAGATC[A/G]TTGAGTCTGCTGTAT | 9690 |
rs544266664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199302 | ACTGTTGCGTATTCT[C/T]AGCAAATAAAACTCC | 9690 |
rs544285917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229786 | TGCCCAGCTTTTCTT[A/G]TATTTTGTAGAGACA | 9690 |
rs544315049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157223750 | CATAGTGAAACCCTG[C/T]CTCTACAAAGAATAC | 9690 |
rs544352341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219510 | AAAATTACAGGAAAC[A/G]TAGGGGTTAGAAGTA | 9690 |
rs544364237 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150797 | AGTTTCTTAATTTCC[A/G]TTGAATAAAAGAAAG | 9690 |
rs544379900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157236163 | GTGTGGGTCATGATT[A/G]CATTTTGTCGCCTGT | 9690 |
rs544384670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251542 | CCTCATCTCAGACGG[A/G]TGTGAGTGCCGGAGG | 9690 |
rs544389469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148065 | ATGAGGATACTCTAG[A/G]GCCTACCAAAACCAA | 9690 |
rs544408603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157245875 | GCACGCCTGTAGTCC[C/T]AGCTACTCAGGAAAC | 9690 |
rs544444568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246269 | CTAAATACGGTAACT[A/G]GTTGGAAGCTGTGAC | 9690 |
rs544446211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240462 | CCAGTTAGTGTAGGG[C/T]CCACTTGACGTTAAT | 9690 |
rs544526705 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157224743 | TTTTGAAGCTGTTCA[C/T]GTCCCTTTACTAAAC | 9690 |
rs544532143 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157218184 | GGCGCGGTGGCTCAT[C/G]CCTGTAATCCCAGCA | 9690 |
rs544534963 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157177468 | CTGTTGCATTATCAG[A/G]TTTACCTCTCACATG | 9690 |
rs544537246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157180118 | TTACACAGAAACTGC[C/T]GCTTCTAGCATCTTC | 9690 |
rs544558196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236702 | CAGAGCTTCTCTTGT[A/G]TAATACCTTGTTTTG | 9690 |
rs544569829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167846 | TGGCCTAAAGTGCCT[C/G]TCATAGGGCTGGCAC | 9690 |
rs544575221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150834 | GTTGCTTATTGCTGT[A/G]TAATAGAGCTTAAAG | 9690 |
rs544583823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157257507 | AAATTGCCTCAGGCA[A/G]ATGGATCATTTGAAG | 9690 |
rs544618179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263205 | CTGCCCACCGTAGCC[A/G]CTATGCTTCGTGTCC | 9690 |
rs544620408 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187867 | AGACATGAGCCACCA[C/T]ACCCAGCCTTCATAG | 9690 |
rs544650697 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157212468 | ATAATATAGCTAGTG[C/T]GTAAGAATATTTCCC | 9690 |
rs544679684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240883 | CAGGATGGTAGAATG[A/G]CAGTCAACTGTGTGC | 9690 |
rs544714130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156497 | TTTTTCATAGAGACA[A/G]GGTTTCACTACGTTG | 9690 |
rs544726699 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183006 | CCCGCCTCGGCTTCC[C/T]ACAGTGCTGGGATTA | 9690 |
rs544751171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156141 | ACTTGTTCCTCATTA[C/T]ATTGAGCTGTTTTTA | 9690 |
rs544767745 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138436 | AGACATAGAACAGGT[G/T]GGATGTAAACAGACG | 9690 |
rs544777239 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157163696 | TAAGTCAAGACAGCT[C/T]GTTTGGATGATCTTT | 9690 |
rs544795554 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157224091 | ATAGCTCACAGCAGC[C/T]TCAAACTCCTGGGCG | 9690 |
rs544800413 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157192703 | ATGAGAATGACAAAA[A/T]GAGCTGCCTTCGTCG | 9690 |
rs544812664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157168787 | CCAGGGGCAAGAGAA[A/G]GGACGGCAGGAAACG | 9690 |
rs544812999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163102 | AAATGATACCCAGAG[A/G]TGGCCGGGCGCGGTG | 9690 |
rs544814955 | in-del | -/TAAAA | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157257809 | GTATTCACTGTAAAT[-/TAAAA]TAAAGCCATATTAAC | 9690 |
rs544818594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179187 | ACCTGACCAGGAAGG[C/G]CTCTTACCACCTCCT | 9690 |
rs544821742 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157139502 | TCGCCGGATCTCGGG[A/G]CCGCTCCGGCCGGGA | 9690 |
rs544831509 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142771 | GGGTAATGGGATCAT[G/T]CACACCCCAAACCTC | 9690 |
rs544832423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157258768 | CCCGGCCCCCCAAGT[A/G]TTTTTTTATATTTCT | 9690 |
rs544849103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156589 | AGCGTTACAGGCATG[A/G]GCACCGCATCCGGCC | 9690 |
rs544850115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157187146 | GATGTAGGATATTCT[A/G]CTGTCCAAGCGTTTC | 9690 |
rs544868657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167091 | TGCACCACCATGCCC[A/G]GCTAATTTTTTGTAT | 9690 |
rs544869611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240942 | AGTGTGTTGGACTCT[A/C]AGGAGCTAAAATCTT | 9690 |
rs544887282 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209167 | AATGCTTGCACTTAA[A/C]CTGATGGGCTAATTA | 9690 |
rs545016055 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269485 | ATAGTAAGATGGCCT[A/C]CACTCACTGAGAATC | 9690 |
rs545017618 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138837 | GTCTGCAGGGCCGCG[C/T]ACGTCTGCAGGGCCG | 9690 |
rs545053281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180898 | AGGCTGATTGTAGGG[C/T]GGGATGCAGGACTGC | 9690 |
rs545057316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193311 | CAAATTATTGCCTTT[A/G]TACTTGTGTGCTATA | 9690 |
rs545073711 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157218863 | GCTAACTCTGAGTTC[G/T]CAAGGGTGCTAACAA | 9690 |
rs545073765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211979 | TCACTTGAGGAAAAC[A/G]GTTGTTTTCCAACGA | 9690 |
rs545076783 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191068 | TGATGTTATAATTTG[C/T]CCGTAGTTTCATTTA | 9690 |
rs545127849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263127 | GCACCTATGCTCAAC[A/G]CACTCAAGCCTCAGC | 9690 |
rs545184741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199966 | GGAGACCCCGTTTGA[C/G]ATTCTGCTCTTACTG | 9690 |
rs545198953 | in-del | -/CAGAAATA | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157216254 | ATTTCTCAGAAAACT[-/CAGAAATA]CTCTTTCAGGAAAAA | 9690 |
rs545207030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150957 | GGCCGTTGGCAGGAG[A/G]GTCAGTTCTCGGCCG | 9690 |
rs545219808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206175 | TTAGCTAAAAGTTCC[A/T]TAAGACAAGGAACCA | 9690 |
rs545227477 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179748 | CTGGGTTACATCTAA[C/T]GGACTTGAAGTCTGG | 9690 |
rs545234226 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186292 | AGCTGGGTGTGGAGG[C/T]GGGCAAGTCCCAGCT | 9690 |
rs545246432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214343 | AGAAAATATATGTTC[C/T]TATGAACAGAGATTG | 9690 |
rs545303843 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191808 | TTAAATATATATACC[A/G]TCCATGTGTTTGTAA | 9690 |
rs545303924 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157158250 | GAAACACAAATATAA[G/T]GAAGCCTTTTGAAAA | 9690 |
rs545304737 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222083 | CATGTGTTGCCCAGG[C/T]TGGCCTTTAACTCCT | 9690 |
rs545329224 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212730 | CATAATAGAGCATGT[A/G/T]TAACAGTTGTGTACC | 9690 |
rs545365849 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146962 | AACCATAGTAAGCAT[C/T]GAAGTCTGGTAGTGT | 9690 |
rs545380629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231500 | TTGTAAGTAGGTGCT[A/G]TGGTTTGAATGTCCC | 9690 |
rs545382700 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157144702 | TTTTAAAAAAAAATA[G/T]ACTTTATTTTTTAGA | 9690 |
rs545386576 | snp | C/G/T | 1.66632e-05 | 0.0028864 | intron-variant | UBE3C | GRCh38.p7 | 7:157169157 | AGGAGATTAGTAGGG[C/G/T]ATGGGAGAGCTTATT | 9690 |
rs545386810 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142845 | CCCTAACTCTAAAAT[A/G]AAAGTTGAATTTTTT | 9690 |
rs545398095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157219530 | GGTTAGAAGTACATC[C/T]TTAACAACACCATGA | 9690 |
rs545426199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190059 | CCCGCCTCAGCTTTC[A/C]AAAGTGCTGGGATTA | 9690 |
rs545483990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266728 | AAAGATAGAATAAAT[C/G]TTGATCCTTTTTAAA | 9690 |
rs545518203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157203 | ATATACAGAAATCCA[C/T]GCTAGTGATGTGGAC | 9690 |
rs545552003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157236824 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 9690 |
rs545585010 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157169828 | TGGGACTACAGGTGC[A/C]TACCACCACAGCTGG | 9690 |
rs545603129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253074 | TTTTTAAAAATTTTT[A/T]TATTTAAAATACACT | 9690 |
rs545606605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220228 | AAAATAAAAAATTGT[A/G]AGGACCAAAAATAAG | 9690 |
rs545638139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253601 | GAGTCGCTTTTTCTC[C/T]TCTGACTTAACGGTG | 9690 |
rs545679368 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199384 | TTAAATATCTCAGAG[A/G]TAGGGTATCTATTAT | 9690 |
rs545703877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157226014 | ATTTCTAAAATTGAC[A/G]GTTACTACAACAGAA | 9690 |
rs545705437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140175 | CCCTCCCTTCCCACC[C/G]CTTCCCATCATTTCT | 9690 |
rs545708527 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137082 | GCTGGGACTACAGGC[A/G]CCTGCCACTATGCCT | 9690 |
rs545738385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145269 | AAAGGAGGAGGCCCG[C/G]CACTTTGGAAGGCCA | 9690 |
rs545744772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227985 | GTGGTGTTTTGCTAC[A/G]CAAATTAGTAAAGTC | 9690 |
rs545753814 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155864 | TAGTTACAGCAGGGA[A/G]CGTGCACGCTGTCAG | 9690 |
rs545766011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222957 | GCATTCGGGCCTCAC[C/T]GCCAGTGCTAGGGCT | 9690 |
rs545775144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147872 | TTGAGCCCGTCTTGC[A/G]TATCTGGAATAAATC | 9690 |
rs545783378 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180029 | TTGTATTTGTTTTCT[A/C]AAATTGTAAGGAAGA | 9690 |
rs545800822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228613 | GAAAGCAAGCTGGAG[C/G]CAAATGGCTTAGATG | 9690 |
rs545815813 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178050 | AAAAAGGATTGGGGT[-/G]GGGGGGAAAGAGGGA | 9690 |
rs545817378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260433 | GAAGCATGACCCATG[C/T]GACCAGATAGGAGAA | 9690 |
rs545822110 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157239961 | AGAGCAGTGTTCCCA[A/G]ACCAGCCACATCTGC | 9690 |
rs545827223 | in-del | -/TGA | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157147940 | TTAGATTGAGCTTGT[-/TGA]TATTTTGTTCAGGAT | 9690 |
rs545829776 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253068 | AAATACTTTTTAAAA[-/AT]TTTTTTATTTAAAAT | 9690 |
rs545851763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157161402 | ATGAAGGTTTTTTAT[A/G]TGAAATTTTCTTTGA | 9690 |
rs545863138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211078 | GCATCCACCAAACTT[A/G]ACAGGAGTTTCCTCC | 9690 |
rs545872075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197708 | CACAAGAATAAAGTC[A/G]AGAGCTGCAAATTCA | 9690 |
rs545880586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239107 | GCTGAAAATATCCAC[A/G]TCATATCACAAGAGA | 9690 |
rs545950032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149999 | TTCGATGGTGGTCAA[A/G]TTACAGGCTGTAATA | 9690 |
rs545952092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143025 | GGCCTGCACCACCAC[A/G]TCTGGCTAATTTTGT | 9690 |
rs546014309 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157207175 | ACAGGTAGCAGAAAC[C/G]TTAGTGAAGATTAAT | 9690 |
rs546038356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157256304 | CGCGCCACAACATCC[A/G]GCGAATTTTTGTACA | 9690 |
rs546039548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229877 | CTTGGCTTCCCAAAG[C/T]GCTGGGATTACAGAA | 9690 |
rs546081858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141812 | TTTGGCTTGGCTTCT[G/T]TCTGAGAGGTGGACT | 9690 |
rs546102140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222419 | CACTTTACTTTTTTT[C/T]TTTCTTTCTTTCTTT | 9690 |
rs546121058 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157235052 | CAAAATTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 9690 |
rs546139464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157148364 | CACCTCAGCTTCCCA[A/G]TGTGCTGGGATTACA | 9690 |
rs546189727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160742 | AAACTTTTGCCCACT[A/G]ATTTTAGCATACATT | 9690 |
rs546234484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157244146 | GAGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGC | 9690 |
rs546248497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203317 | GCTAAAGCAGAGACA[A/G]AAGACTCCTACAATG | 9690 |
rs546278614 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259612 | CTGTGCTAAGTGAAC[A/G]AAGCAAGACACAAGA | 9690 |
rs546283986 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157266037 | AGGGGAACTGGGGCC[A/G]GGCACGGTGGCTCAC | 9690 |
rs546299759 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236571 | AAAAGTTGGAAAGTT[C/T]CTTTTTCTCCATCAT | 9690 |
rs546319169 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243417 | TGCAAGGCAGAGTTG[C/T]TCTTTTTCTCTGAGT | 9690 |
rs546353910 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157149545 | CGGACCCTGCACTGG[C/T]ACATCCCTGAGAGTG | 9690 |
rs546364078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172994 | TTGACTTTCGGCCTC[A/G]AGCAAATATCAAGCA | 9690 |
rs546368181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166887 | TACATTGCCATGTGC[A/G]TCTGGTGAAAGTCGC | 9690 |
rs546400831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185690 | TAAGCTCTTTTGCCT[G/T]TAGGTTTCTGTATAA | 9690 |
rs546409890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157260537 | TAAAGAGCAGGAGGA[C/T]TGCAGGTGAGGCGTG | 9690 |
rs546429172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157203439 | AGCCACTTCTGACTA[C/T]GCCAGCTTTGGTTTT | 9690 |
rs546434697 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157198274 | TTGAGGTGGTGTCCG[G/T]GGGCTCTTGAAGACT | 9690 |
rs546467393 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205277 | GATGCATTCCTTTTG[C/T]TTGTTTCACAGGGGG | 9690 |
rs546473404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229506 | GTATTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9690 |
rs546504633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209902 | GAGTTAGGGCAAGGC[C/T]GGGTGTGGTGGCTCA | 9690 |
rs546559743 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159705 | AACCTTGTCTCTACT[-/A]AAAAATACAGAAACA | 9690 |
rs546587921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157255951 | GGGAAAACACCCAGC[C/T]GTGTTAGTACTAGAC | 9690 |
rs546590002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171767 | GCTGGAATGCAGTGG[A/C]ATCATCTCGGCTCAC | 9690 |
rs546593212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255358 | GTTCTAAAACTGGAT[A/T]GTGCTGATGGTTGCA | 9690 |
rs546601111 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157243156 | GACAGGAGATGTGCA[C/T]GTGTCCTCCACGGTC | 9690 |
rs546654663 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157136967 | GAGTCTCCCTCTGTT[C/G]CCCAGGCTGGAGTGC | 9690 |
rs546670005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260008 | TCAATCATCGACGCC[A/G]TTATGTTCTGGAAGT | 9690 |
rs546699649 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154439 | CAAGTCTAAACATAA[A/C]CATGTCCTCCCCTCT | 9690 |
rs546717634 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157141961 | CTAGATGATACGCAT[A/G]TTCAGCTGTTGTGCA | 9690 |
rs546741255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157190831 | ATACTTTTTCTCCAA[C/T]CATAAATGAGGCAAA | 9690 |
rs546758893 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157239384 | ATGGAAGTTCAGAAA[C/T]AAGCAAAGCTCCTTG | 9690 |
rs546773477 | snp | A/C | 8.84165e-05 | 0.00664834 | intron-variant | UBE3C | GRCh38.p7 | 7:157181485 | TATTACAGGAAAAGG[A/C]ACTAAATTTTAAATA | 9690 |
rs546800592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157250880 | CTGAGGCCTTTGCTA[A/T]TGCGAGTATTTCCCA | 9690 |
rs546800821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157245428 | CTTGGCTTTGAACTC[A/G]TCATTCATTTCGAAG | 9690 |
rs546803070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244202 | GCCATTCATTGCGCT[C/G]CAGCCTGGGCGATAG | 9690 |
rs546805362 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266693 | ATGATTTGGTTAACC[C/T]GAGTAATAGCTTGTA | 9690 |
rs546811904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196659 | CTGTTGCTGTTTATC[A/G]TATCTTCTTAAGAAT | 9690 |
rs546817640 | snp | A/C | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269832 | TTAAGGCAGCTTTAT[A/C]GATTGCAGTGGTTTA | 9690 |
rs546823373 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157166991 | CTGGAGTGCAGTGAC[A/T]TGATCTCAGCTCACT | 9690 |
rs546857143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167599 | CTGGAATGCAGTGGC[A/G]CGATCTCGGCTCACT | 9690 |
rs546882520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224160 | ATTACAGGCATCAGC[C/T]ACTACACCTGGCCTG | 9690 |
rs546886697 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138076 | TATGCACATGTATAT[A/G]AGATATTATGTATAC | 9690 |
rs546889536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157217339 | TTTTTTTTTTTGAGA[C/T]GGAATCTTGCTATGT | 9690 |
rs546919303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223820 | AGCTACTTGGGATGC[C/T]GAGGTAGGAGGATCA | 9690 |
rs546936541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223445 | TCTAAAGGTGCCTAG[G/T]GCCTGGCTGATTACA | 9690 |
rs546938645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261172 | TCAGCCGGGCATGGT[C/G]GTGCATGCCTGTAGT | 9690 |
rs546961327 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264763 | TTTAGTAGAGATGGG[C/G]TTTCGCCATGTTGGT | 9690 |
rs546962284 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170981 | TAATGTTAAGGCTAA[-/T]TTTTTTTTTTTGTAG | 9690 |
rs546964710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157249422 | CCGGGTTCAAGTGAT[C/T]CTCCTGCCCCAGCTT | 9690 |
rs546971669 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157217897 | CATGGTAAGTGTCCC[C/T]CTGTAGTCCCAGCTA | 9690 |
rs546977317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157235087 | TCCCAGCTACTCCAG[A/G]GGCTGAGGCAGGATA | 9690 |
rs546994636 | in-del | -/A | 0.322959 | 0.239117 | intron-variant | UBE3C | GRCh38.p7 | 7:157204399 | GGGAAACTTTGTTTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs546994850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237495 | ACAAGGTAAATTCTT[C/T]CTGCCCTTGGATTAA | 9690 |
rs547009480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191257 | TGCACGCGCGTGTGT[A/G]TGTGTGTGTGTAGTG | 9690 |
rs547012691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256566 | TTTGCATTTACAATC[A/G]GTCCTTCATATCTGT | 9690 |
rs547029782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157240053 | GGAACTCTAGGGCTA[A/G]GGCTCAGCAAGCTGT | 9690 |
rs547035326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264139 | GTTACGTGCACACAC[A/G]CACACCTGGTATTAC | 9690 |
rs547042595 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148500 | AACTGCCCTCTATTA[C/T]ATAATTGAAGGGATT | 9690 |
rs547045852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197785 | TACTATTGAATCTTT[A/G]TATCAAACGACTCCC | 9690 |
rs547066577 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203702 | AGGGTAGTTTTACAA[A/G]TCTTATTAAAAGACA | 9690 |
rs547112658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194359 | AACCCTAGCACAGGT[A/G]ATTTCACCTCTTTGA | 9690 |
rs547127531 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157218389 | GGGATGCGGAGGTTG[C/T]AGTAAGCTGAGATCA | 9690 |
rs547141877 | in-del | -/CAAAAAATT | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157152927 | TTGCCAGGTGTGGTG[-/CAAAAAATT]ATGCACGCCTGTAAT | 9690 |
rs547144642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157267111 | AGTTAGAACTAAGCC[A/G]TCAATGTAATTTTTT | 9690 |
rs547148683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157227324 | CTGTGGTCAGGGGTA[C/T]TTGCAAGTGGGGGGG | 9690 |
rs547173993 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214621 | ATCAATTTAATTGGT[C/T]ACAAAAATGGAAAGA | 9690 |
rs547200217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247606 | CTGAGGCAGGAGAAT[A/C]GCTTGAACCTGGGAG | 9690 |
rs547225250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157177567 | CCTTTGCGTCCCAGC[A/G]GCTTGTTATGTGTAG | 9690 |
rs547228439 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157179362 | AGGATATTTAGTTTG[A/C]ATTTTCTAACTCAGT | 9690 |
rs547234001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220950 | CTCTAGCTCCATTGC[A/G]GCCACCTCTTCAGCA | 9690 |
rs547235032 | in-del | -/T | 0.140581 | 0.224783 | intron-variant | UBE3C | GRCh38.p7 | 7:157148107 | TTTTGTTTTATTTTG[-/T]TTTTTTTGAGACAGA | 9690 |
rs547256206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176402 | GCTTCAGCCTCTCAA[A/G]TAGCTGGGACCACAG | 9690 |
rs547300775 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140058 | CAAACCATGACGCCT[C/G]TGTTCTAGTCTAGAA | 9690 |
rs547302785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145517 | GAGTGATACTCTTTT[A/T]AAAAAGAAAAAAGGA | 9690 |
rs547329836 | in-del | -/ACATATAGC | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157217138 | CAACTTCTTAATGGA[-/ACATATAGC]AGTATCATTGACTTA | 9690 |
rs547350482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158851 | TAGACTCCAAGTGTG[C/T]TGAATGGTAAAAGCA | 9690 |
rs547399160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240329 | CAAAGTGCTGGGATT[A/G]TGGGTGTGAGCCATA | 9690 |
rs547406613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181186 | CTAGATATTTGTGAT[A/G]TTAAGGAACTACTCT | 9690 |
rs547406650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188413 | TTACCATCGGAGGAA[A/G]TAGATGTCAGTGAAA | 9690 |
rs547407782 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217656 | CCTGGCCAACATGGC[A/G]AAACCCTGTATCTCT | 9690 |
rs547442809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193612 | AAGAATATCACTTCT[G/T]TACATTTTAGAAGTA | 9690 |
rs547479175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200374 | ACTCAGAAAGTGCCA[A/G]TATGGAACAATGCAT | 9690 |
rs547496436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243207 | CCCTGCAGGGCTTCC[A/G]AAGTGAAAGCCGAGT | 9690 |
rs547497626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157438 | ATGATTCAAACTGTG[A/G]AAACATAAAAAGTTA | 9690 |
rs547529221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164943 | TTAGGCAGGATTTTC[C/T]AACCTTGGTGCTGAC | 9690 |
rs547531236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247828 | GCAGAGTGGCATATG[C/T]GGTTATGAACTGGGA | 9690 |
rs547570846 | in-del | -/TTC | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157169228 | ATGCTGACAGTAGTA[-/TTC]TTCCCAATAAATAAT | 9690 |
rs547610166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189676 | TCCTGACTCTTTCAG[C/T]GGCTTCTTTCATAGA | 9690 |
rs547627376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147284 | CGTTTATTTTTAAGG[A/G]GTGCTAATGTGAATG | 9690 |
rs547656098 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218531 | AATTTTATAAGCATG[A/G]CTATGTCCTCATAAG | 9690 |
rs547684893 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177085 | ACATAGTAGTTATAT[A/G]TTTCACTTTAGAAGA | 9690 |
rs547698576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226330 | TGGAGCTCACTGGCA[C/T]GTTTCGTCGTATGTT | 9690 |
rs547706253 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157259211 | TGGGAGCGGAGCCCC[A/G/T]CAGTCACGTTGTGAC | 9690 |
rs547717826 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218889 | AACAAAACCCTTCGT[C/T]ATCATATTTGTAGGA | 9690 |
rs547747413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195737 | TTTGAGACTTTTGAG[A/T]TGGTGAGACTCAGAT | 9690 |
rs547754928 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157242848 | AATCACGAGGTCAGG[A/G]GTTCTAGACCAGCCT | 9690 |
rs547831123 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157146414 | TCTAGTACAGACGGG[G/T]GTTTCACCATGTTGG | 9690 |
rs547849074 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148994 | CTTCGAATACAGTTA[C/T]GCTGTATCCTTTACA | 9690 |
rs547858462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209022 | TGCTTTTGTCAAGCT[A/G]TCTATTTAATTGAAA | 9690 |
rs547877612 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157232519 | CACGCCCAGCTAATT[C/T]TTCTATTTTTAGAAG | 9690 |
rs547885881 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173854 | ACCTCAAGAGAAAGC[C/T]TGTGTGTAGGCAAAT | 9690 |
rs547897302 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157208211 | TCCTGAGTAGCTGGG[G/T]CTACTGGCACATGCC | 9690 |
rs547912486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189016 | AGACAGATGCGTACA[C/T]GAAAACCGGGAAGAC | 9690 |
rs547926027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207592 | TTTGCTGCTGGCCAC[G/T]TGGCCCATCAGTTTT | 9690 |
rs547932492 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157242093 | GGTCATACAACTTTA[C/T]GAATATAATAAAACC | 9690 |
rs547980735 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198431 | TCACATTAAGTTCTG[C/G]AAATCCTGTGCGCTC | 9690 |
rs548057309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254679 | GCCAGGATTATGGGC[A/G]TGAGCCACCATGCCT | 9690 |
rs548059453 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146686 | AATTTGAGAGGGAGC[C/G]TCCTGTTGCCCAGGC | 9690 |
rs548068607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221569 | AACATAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9690 |
rs548081664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195254 | TGTAAATGAGTGAAT[A/C]CCCATGACATATGTA | 9690 |
rs548102097 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194558 | GGAAGAATTCTGAGG[C/T]GCATGCCAGAAAGAA | 9690 |
rs548105275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221041 | CATGCTGTGTAGTCT[A/G]CTCCTGGCTCCTTTT | 9690 |
rs548137931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140456 | GAAGTCACTTGTGCT[C/G]CAGAACTAAGTACTG | 9690 |
rs548151140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232715 | TTAATTTCTGTAAGA[A/G]TCAGAGCTATAATCA | 9690 |
rs548154422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261029 | ATAGACTGGCCAGGT[A/G]CGGTGGCTCACACCT | 9690 |
rs548166036 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157243619 | TCCTGCATGTGAGGC[A/C/G]CAGGGGACACTGGGA | 9690 |
rs548169593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157259623 | GAACGAAGCAAGACA[C/T]AAGACTACGTATTAT | 9690 |
rs548196536 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196862 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9690 |
rs548202840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157239243 | ATAAATAAATTGTAG[A/G]ATATTCACAAGACTT | 9690 |
rs548231252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219158 | TCTAGGGTCTGCTGG[C/T]CTGAGATGGTGTGTT | 9690 |
rs548243585 | snp | A/C/G | 4.94233e-05 | 0.00497087 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182269 | GTAGATGTTCAAGAA[A/C/G]GAGTGGTGGAGCACC | 9690 |
rs548300907 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261957 | GAACTTCATTTTTTT[-/A]ACTTTTAAGTCTCCA | 9690 |
rs548304507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231901 | AGGACTGCCGCAACA[A/G]ATTACCACACTCTTT | 9690 |
rs548318982 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157208369 | GCGTGAGCCACTGCA[C/G]CTGGCCTATATACCT | 9690 |
rs548334114 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192076 | AATCCTATCTAGATT[A/G]TAAACTAATTTCCAC | 9690 |
rs548337978 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216750 | CGGGTTTGGTGTCCG[A/G/T]CTCGACCTGGGTTCC | 9690 |
rs548342032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157266948 | GGTCTCGTTATGTTG[C/T]CCAGGCTGGTCTCGA | 9690 |
rs548368608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177649 | GAGGGGAAAGTTGTG[A/T]AAAGGGCAAAGACAA | 9690 |
rs548387995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170908 | AATTCCCAGGCTTAA[A/G]CAGTCCTCCCACCTC | 9690 |
rs548426352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176981 | GTAAATGTGGCCTTC[C/G]AGAACCACCTGCAGC | 9690 |
rs548435325 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238458 | GAAGTCATCATATTC[A/G]AGGAGATTTGCTGAT | 9690 |
rs548439474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165919 | TGGGGTTTCCTTTAT[A/G]GGTGACTAGCTGCTT | 9690 |
rs548457259 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157215285 | AGTACCCTTCCCCTT[C/T]TTTCTTGGGCACACA | 9690 |
rs548497646 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157266245 | CGTGAACCCGGGAGG[C/T]GGATGTTGCAGTAAG | 9690 |
rs548499685 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198596 | CTGAAGTGCAGTGGC[A/G]CCATCTCGGCTCACT | 9690 |
rs548533331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183793 | AGAAATGCCTCTCTG[C/T]GTGTGAGGAAAAATG | 9690 |
rs548538054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163150 | CAGCACTTTGGGAGG[C/T]CGAGGCGGGTGGATC | 9690 |
rs548551363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238729 | AGCCTGAATTAGATC[A/G]CCCAGGGTGTAGGTG | 9690 |
rs548573590 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157162518 | TTTTTGTAATGATTC[A/T]TATATAGTGTCTCCA | 9690 |
rs548588254 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157206286 | ATTTTTTTTGGAAAC[A/G/T]GAGTCTCGCCCTGTT | 9690 |
rs548593479 | snp | A/G | 1.6569e-05 | 0.00287824 | intron-variant | UBE3C | GRCh38.p7 | 7:157178850 | ATGATTCACAATGGT[A/G]AGTAGTAGGCAGGAT | 9690 |
rs548629210 | in-del | -/ACAC | 0.0491847 | 0.148907 | intron-variant | UBE3C | GRCh38.p7 | 7:157264239 | CATGCTCGGCCTGTT[-/ACAC]ACACACACACACACA | 9690 |
rs548638952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157233851 | TGACTCCACATCGTT[A/G]TCAGCACTTACTTAG | 9690 |
rs548641795 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187048 | TGGGCGTCTGTGCCA[-/G]GGGGTGCCAGCCAGA | 9690 |
rs548644331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202634 | TGCAGTCCAGCCTGG[G/T]TGAGAGCAAGACTTC | 9690 |
rs548651632 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157162319 | TCTCCCTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 9690 |
rs548678356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235921 | AGCAGCTGATAGTGT[A/G]GCACCTGAACATTAC | 9690 |
rs548727822 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157156371 | GAGTGCAGTGGCATG[A/G]TCTCGGCTCACTGCA | 9690 |
rs548734722 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269269 | CTGAAGAGAAATTGA[A/C]AATTCACTTATTTGT | 9690 |
rs548871379 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189805 | TATTCAGTTTTTTAG[G/T]GTTGTTAGTTTGTGA | 9690 |
rs548897153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156631 | ATCCTTACATTCACA[C/G]TCTATTTTGGGATTT | 9690 |
rs548898629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228154 | TGCTCGTTGTCTTAT[C/G]TCCGAACGATTCTCT | 9690 |
rs548902911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196410 | GAAGGGAAACCTTCT[G/T]ACTTCAGAAATACAA | 9690 |
rs548908256 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157258031 | CGGCTCACTGCAGCC[A/G/T]CAGCCACCCAGGCTG | 9690 |
rs548914589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189904 | CTCCAGGGTTCAAGC[A/G]ATCCTCCTACTTCAG | 9690 |
rs548970904 | in-del | -/AAAC | 0.498859 | 0.0238584 | intron-variant | UBE3C | GRCh38.p7 | 7:157153827 | CTAAAAATACAAAAC[-/AAAC]AAACAAACAAACAAA | 9690 |
rs548985722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240994 | ACCCGGGAGAGGTAA[C/T]GGATGCGCAAGCCCA | 9690 |
rs548988985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157175295 | TGAATTATCTTGTGA[A/G]TGATGGCCATCCTGG | 9690 |
rs548993939 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156806 | TCGGAGACAGTTCCT[G/T]ATCAGTAGATAGATC | 9690 |
rs549008656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157192299 | AAGTTTTCTTTTAAG[C/T]TTGTTAAGAAATAGT | 9690 |
rs549039659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198722 | GTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 9690 |
rs549053419 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181894 | TGCTTTTCTAAGTAA[C/T]TGTCAAAAATTAACG | 9690 |
rs549114392 | in-del | -/TTAG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157222185 | CTGTGAACATGTTTT[-/TTAG]TTATTGAATTTTGAG | 9690 |
rs549172653 | snp | A/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141988 | TGCACACCGCTGCCA[A/C/T]AGTTTCCCCGTGTCG | 9690 |
rs549203106 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157230794 | ATCGGCCTGTGGGCT[A/G]CAGGTTGAGGACAAG | 9690 |
rs549223458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192718 | TGAGCTGCCTTCGTC[C/G]AGAGTGCCCTTCTGA | 9690 |
rs549226676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144749 | AATCAAGCAGAGGGT[A/G]GGGTTCCCATATGCC | 9690 |
rs549228815 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225650 | TGTTCCATAATGACT[G/T]AAAAACTGAAATGTG | 9690 |
rs549236849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219310 | TGATTTATATTTTGG[C/T]ACAAGTCCCTTATCT | 9690 |
rs549308256 | in-del | -/TTTTT | 0.00159712 | 0.0282137 | intron-variant | UBE3C | GRCh38.p7 | 7:157165398 | TCTTTAGCATTGACT[-/TTTTT]TTTTTTTTTTTTTTT | 9690 |
rs549335834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252666 | GTGAAACAATCTTTC[C/T]GTAAATGGTAAGAGA | 9690 |
rs549336799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151122 | GGGGTGAGGGGAGTC[A/G]GGCTCCACCCCCTAA | 9690 |
rs549357045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157241520 | AGCCACAGGCTGCCG[C/T]GCACACCCGCGAGTA | 9690 |
rs549367832 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235810 | TCCTAAGGGGTTACT[A/G]ACTTCCAAAACATAT | 9690 |
rs549375003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157236425 | ATGATCTTGGTTATA[C/T]ATTTGAAAATTTCAA | 9690 |
rs549378978 | snp | A/C/T | 0.000216798 | 0.0104095 | intron-variant | UBE3C | GRCh38.p7 | 7:157188981 | GGAGACCTTTGTACC[A/C/T]TGACATGGAAAGATT | 9690 |
rs549419843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241092 | AGGAGCACAGGGGGC[C/T]TACCTCCCTTCTGTG | 9690 |
rs549424945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214402 | AGACCTGATCTTTCC[A/G]TTGCCTGACCTGGAG | 9690 |
rs549463452 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268859 | CTACAAACAGAAAGC[A/G]TTTCAAAGCGTCAGC | 9690 |
rs549495334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258604 | AGCTGTGATTACAGG[C/T]GTGCGCCTCCATGCC | 9690 |
rs549526619 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212966 | TTTCACCATGTTACC[C/G]AGGCTGGTCTTGAAC | 9690 |
rs549529985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237600 | TGAAATTCATGAGAA[A/G]AATGGATCAGTATGG | 9690 |
rs549530172 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157264604 | ATATATTTTTAAGAC[A/C]GAGTTTCACTCTTAT | 9690 |
rs549569418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259070 | TGAACTCTGACATAC[A/G]GCACTTACCTTATCG | 9690 |
rs549571174 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170670 | AAAATAGGCTTTTTC[A/G]TATTTTTTGCAGTGG | 9690 |
rs549595395 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180120 | ACACAGAAACTGCCG[C/T]TTCTAGCATCTTCTG | 9690 |
rs549615370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214644 | TGGAAAGACCAGACA[C/T]GAACATCTTCATACA | 9690 |
rs549697332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164104 | GACTTACATAATGAT[A/G]TGGTTTCCAGAAGAT | 9690 |
rs549697890 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157151826 | TGACAACCGTGGAGC[A/C]GGAGGTAGCCACATC | 9690 |
rs549741181 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234692 | CAACCTGACTTCACT[A/G]CCGTAACGGTATGTG | 9690 |
rs549751593 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209571 | GGTGTTAACGGTAGC[A/G]TATTTGTTTTCCTTT | 9690 |
rs549822995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175892 | TTATGTAAATGGCGA[C/G]ATAGCAAATATTTTA | 9690 |
rs549836494 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157244246 | CTCGAAAAAAAAGAA[-/AG]AAAGATGAGGTATAT | 9690 |
rs549841945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157144539 | TGGGAGCAGGCAATG[A/G]GAAATATTTTGAGAC | 9690 |
rs549845290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192835 | AGAAGACAAGTAACT[A/G]CGTATGAGTTAATAA | 9690 |
rs549845839 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246147 | ACGAGTCCTTAAAAT[A/G]TGAATCTCAAGGGGT | 9690 |
rs549856725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205887 | CCTGAACCATGCACC[A/G]TGGAGACTCAGAAGC | 9690 |
rs549884320 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157265775 | GAGCACTTAAGACGC[C/T]GAAGCGTTGGTTGCC | 9690 |
rs549897780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163198 | AGACCATCCTGGCTA[A/G]CACAGTGAAACCCCG | 9690 |
rs549914107 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139930 | GTTTGAATCCAAGAC[G/T]AGGGCAATTATTTGC | 9690 |
rs549953184 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143087 | GGTCGGGCGGGTCTC[A/G]AACTCCCGACCTCAG | 9690 |
rs549955944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189065 | GAACCGGCTTTTCCT[A/G]TAAGAAGGATGGAAA | 9690 |
rs549963635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219718 | ACCCTGGCCAACATG[A/G]TGAAACCCCATCTCT | 9690 |
rs549994844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195224 | TTCCAGGAAAGATAT[A/G]TGAGGAGCCTCCTGT | 9690 |
rs550019206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187485 | TTCCTGGGCTCAAGC[A/G]ATCCTTTCACCCCAA | 9690 |
rs550031221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194584 | AAGAAGCCAAATTGC[C/G]TTAAACAGACTGTTA | 9690 |
rs550039674 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269293 | TATTTGTGGTTTTTT[C/T]CTCAGCTATTCTGAG | 9690 |
rs550084774 | snp | C/G/T | 0.000165289 | 0.00908957 | synonymous-codon, missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231288 | TGTGGGAGATTCTTT[C/G/T]GCCAGACATTACTAC | 9690 |
rs550120273 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157187644 | GCAGTGGCGCGATCT[C/T]GGCTCACTGTAGGCT | 9690 |
rs550123875 | in-del | -/ATTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235960 | AGAAGAAAACTGTAT[-/ATTG]ATTGATTGATTGTGA | 9690 |
rs550135724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164796 | AGACAAGGTTCCTGC[C/T]GTGAACCAGGATGCT | 9690 |
rs550175968 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157201814 | GATCACAGGGTATGT[A/G]TTATACAGACTTATA | 9690 |
rs550197319 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252370 | TGGACTGTCAGCTGA[A/G]TACAAGCAAAGGAAT | 9690 |
rs550215925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242254 | TTCATGGATGCTTTC[C/G]TTCTAAAGCTGGAAG | 9690 |
rs550219004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172310 | AAGTGCTGGGATTAC[A/G]GACATGAACCACCAC | 9690 |
rs550255707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157165315 | CTTTTCTCTGTGTTT[A/G]TCCTTTTGAATATCT | 9690 |
rs550283890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249541 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCTG | 9690 |
rs550284827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183482 | GAGTTTTATGGTGCT[G/T]CTTCTCCAGTGTCCC | 9690 |
rs550317836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214051 | CCCATCCTTAACATA[A/T]CTCCCTTGGCTGGAC | 9690 |
rs550365393 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215836 | AGAACTTCAGGTCTT[G/T]TTAAAGTAATGCTAT | 9690 |
rs550370736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152765 | GCCGGCACATCTTGC[C/T]TCTGTCTCCTGCTTT | 9690 |
rs550404999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197951 | TTGCCCTTCTCCACT[A/G]AAAGCCTTGAACCTC | 9690 |
rs550407671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152416 | GCCTGAAGCCAGGGA[A/G]ATCAAGGGAGAAGCA | 9690 |
rs550477412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203516 | AGGACAGGAAATTAT[C/T]GTTTACCCATAAGTG | 9690 |
rs550520383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224396 | AGACGGGGTTTCGCC[A/G]TGTTAGCCAGGATGG | 9690 |
rs550609234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157244235 | TGAAACTCCGTCTCG[A/G]AAAAAAAGAAAGAAA | 9690 |
rs550628275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157192212 | GAATGATAATTGTTT[C/T]CCGGGAAATATGAGT | 9690 |
rs550658003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142591 | GGGTGTGTGGAGTAC[A/G]TGTAGATTGGATTAC | 9690 |
rs550668071 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138160 | TGGCTCAACTTACAA[C/T]TTTTTGACTTTGTGA | 9690 |
rs550672631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217001 | TCTTTTTAATATTTA[G/T]CATTAAAAAATACAT | 9690 |
rs550685440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217423 | TCCCAAAGTGCTGGG[A/G]TTACAGACGTAAGCC | 9690 |
rs550691221 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137126 | GGTATTTTTAGTAGA[A/G]ACGGGGTTTCACTGT | 9690 |
rs550701386 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137000 | TGGCGCGAGTGGCGC[A/G]ATCTCGGCTCACTGC | 9690 |
rs550734189 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142549 | GGATGGGTGGAAGAC[A/G]AGAAGGCATTCCAGG | 9690 |
rs550767037 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157185290 | TGCAGGCTCTCACTC[C/G]TGCTCACACTTTGAA | 9690 |
rs550777127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143276 | TGTTTTTCTTGGTAG[C/T]GTATAGAAGAATATC | 9690 |
rs550803254 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262012 | GAAAGAAACACTAAA[A/G]TGTGGCATTTAATTG | 9690 |
rs550830338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229626 | CCGGCCTGTTTTTGG[A/G]GTTTTTAAATTTTTA | 9690 |
rs550847508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239805 | GTCTGGTGCTGAAGC[A/G]GGGGGCGCCACAGGC | 9690 |
rs550855310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156456 | GGACTACAGGCGCAT[A/G]TCACCACCCCCGGCT | 9690 |
rs550860644 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244003 | TTGGGAGGCCGAGGC[A/G]GGTGATCACCTGAGG | 9690 |
rs550875118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246068 | AAGCCAGTGGTACTC[C/T]AGATGTTTGCTTTTG | 9690 |
rs550881613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162696 | GGGCACATACTGCTG[C/T]ACCCAACTATTTTTA | 9690 |
rs550909561 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157143871 | TGGGACAGGGTGGGA[C/G]TCGTGAGGTACTGCA | 9690 |
rs550914024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168028 | ATGCTGGTGTTGTCT[C/G]CTTGTATTCCTTTAA | 9690 |
rs550915724 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157139579 | GGGGCTTAGGACTGG[A/C]CTCGGGGCCTCCCTG | 9690 |
rs550938804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205308 | TTTGAAGAGGACAAA[G/T]AAGTTTTTGTTGGTT | 9690 |
rs550958121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262520 | GCCTCCTGGGTTCAA[A/G]TGATTCTCCTGCCGC | 9690 |
rs550958473 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157163045 | TGATTTCTTCATTGA[A/C]ATTTTTATTGAGATA | 9690 |
rs550965813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167561 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 9690 |
rs550999173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257194 | CTGGTTATGATGTAT[A/T]TATTTTGGTGCTAGT | 9690 |
rs551051411 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244275 | TATCTCCTGCCCCCT[A/C]GGAGTTTAGAGTTAG | 9690 |
rs551071777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244987 | AGTTTTTGAAGTTGT[A/G]TAATTAACCTGTGTT | 9690 |
rs551079336 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267980 | TAAAATAACACGTTA[C/T]GTGCCATGTGGCTAC | 9690 |
rs551080374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157160971 | CTTACTGTAATCATG[A/G]GAGTATTGGAAAAAC | 9690 |
rs551106867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250143 | CCGGGAGGTGTGATG[C/T]CTGATGAACTGGCTG | 9690 |
rs551121722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261910 | GTATTTAATTATGCA[C/T]AAAATGGTGCCCTTG | 9690 |
rs551128107 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248242 | ATCAGCTTCCATCTT[C/T]GGTACTATGAGGAGA | 9690 |
rs551129578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157149705 | GGTTGAAAAAATAGA[C/T]GGTCTCATAAGACCA | 9690 |
rs551134474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251834 | AAAAGTAGTGTAACC[A/G]TTTAAAAGTTATTAG | 9690 |
rs551151910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157186007 | ATATGAAAAAAGTAT[A/G]TATCTTTGGTTACTG | 9690 |
rs551171728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246548 | TTTGGTATTCCCTGG[A/G]TAGCACCATAGCACT | 9690 |
rs551177326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168485 | CCACAACAAAACTTA[C/T]ATATGAATGTTCATA | 9690 |
rs551216121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157174534 | TCACTGCAACCTCCA[A/C]CCACACCCCGCAAGT | 9690 |
rs551234143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191439 | TGGGACGATAGGCGT[A/G]CCACCACACCTGGCT | 9690 |
rs551249224 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268187 | GACGCCATGGGGCCG[C/T]TGCTGCTTATGTGGT | 9690 |
rs551260543 | in-del | -/TTTTTTTTA | 0.355525 | 0.226637 | intron-variant | UBE3C | GRCh38.p7 | 7:157236240 | AATGTCATCTTGAAC[-/TTTTTTTTA]TTTTTTTTACAGATA | 9690 |
rs551261626 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157202019 | TTATAGAGAGTATGG[-/T]TTTATCTGAAGGTAA | 9690 |
rs551261949 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138598 | CCGTGCCTCGCACTC[C/T]ACCTTTCCCGCACCC | 9690 |
rs551289404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162420 | GGCTGGTCTCGAACT[C/T]CTGACCTCATGATCT | 9690 |
rs551297329 | in-del | -/AGGGA | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157241043 | AGGGATTTTAGCGGG[-/AGGGA]AGGGAAGGGAAGGAT | 9690 |
rs551320232 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174488 | GGTCTCTCTCTCTCT[C/T]GCCCAGGCAGTGCAG | 9690 |
rs551333427 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223766 | CTCTACAAAGAATAC[A/G]AAAGTTAGTTGGGCG | 9690 |
rs551345071 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267408 | GCCTGGGCGACAGAG[C/T]TAGACTCCATCTCAA | 9690 |
rs551396735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198023 | ATCCCAATTCACTTG[A/G]CCACCATGAACAAGG | 9690 |
rs551413109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155673 | TAGTGAAGAAAGCAT[C/T]TTCCCCCCATTTGAA | 9690 |
rs551460196 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137898 | TATCGTATTGTGTGT[C/T]GAAATTTTGCTAAGA | 9690 |
rs551564098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156239 | TGATCATTCAGATGG[A/G]AATGTAAACAGTCAA | 9690 |
rs551569087 | snp | G/T | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139982 | GGAGAGACTCCGGAC[G/T]TACATCTGTTGTGAT | 9690 |
rs551583602 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157262664 | GACCTCCGGTGATCC[A/T]CCCACCTCAGCCTCC | 9690 |
rs551607846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235881 | GTGCTAACCATTGCT[C/T]GGATCTAAGTAAGTG | 9690 |
rs551611564 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186269 | TCTCTACTAAAAATA[C/G]AAAAATTAGCTGGGT | 9690 |
rs551645948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157156822 | ATCAGTAGATAGATC[C/T]ACCACATTCCTTTAA | 9690 |
rs551666226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241122 | GCCCGGTGGTTCAAG[C/G]GTGCAAAAGAGACCA | 9690 |
rs551679883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213124 | CTGCATTTATTTAAT[A/G]TAACGTTTTGATCTG | 9690 |
rs551689646 | snp | C/T | 2.08479e-05 | 0.00322855 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186971 | CACCACCATGGCCTC[C/T]GTCTGCCACACGCTG | 9690 |
rs551690298 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157192698 | GGTGGATGAGAATGA[-/C]AAAATGAGCTGCCTT | 9690 |
rs551711102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219259 | GTGCGATGGGAAAAT[A/G]TCAGCTGAACCCAGC | 9690 |
rs551733614 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157174594 | AATAGCTGGGACTAC[C/T]GATGTGTGCCACCAC | 9690 |
rs551763590 | snp | C/G | 0.0126979 | 0.078662 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139178 | CTGCCCCGGGCCGGG[C/G]GGGCGGGCGCCGAGA | 9690 |
rs551768592 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157180181 | CGATAAAATTTTAGC[C/T]TTTTAAATTATAGTA | 9690 |
rs551769656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257931 | ATAGGCATTCACTTT[A/C]TTTTTTCCTTTTTTC | 9690 |
rs551817838 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243644 | CTGGGACAACACGGA[C/T]TTTTTAGTGCCAGGG | 9690 |
rs551832681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246628 | TCCTGCAGCACAGCT[C/G]ATAGTAGTCATTTGC | 9690 |
rs551848468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225009 | TATCGCAAGGGGTTT[A/G]AATTTTAATTTTATT | 9690 |
rs551849774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221217 | ACGAGTACAGCTGCT[A/G]TAAACATCTATGTAC | 9690 |
rs551852145 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268699 | TTGGGGGTGACTCGC[A/C]ATGCTTGGCACCCTC | 9690 |
rs551904764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144383 | GGGAAATTCGGTGTC[C/T]CGGAAATAGTTTTGT | 9690 |
rs551932651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157246960 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 9690 |
rs551935816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257284 | ATTGTGGTTATGATT[A/G]CCTGTGAACAAACCG | 9690 |
rs551937621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230627 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9690 |
rs551978305 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140297 | GGGTGCTGGCAGGCC[A/G]AGGAGGAACTGCTGT | 9690 |
rs551981196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227486 | GGCAGATCACAAGGT[C/T]AGGAGATCGAGACCA | 9690 |
rs552065126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248847 | GAGGCTGCGGCCCAG[C/G]CTTGCTGCTTGTCTG | 9690 |
rs552093118 | in-del | -/TTAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251252 | TGTCAGCAGGTTATG[-/TTAA]TTAATCATCCCTTTT | 9690 |
rs552105794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243682 | GTAGACCAAGTGTTG[C/T]GGGAGTTGATGGTGT | 9690 |
rs552146057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168574 | AATGGAGGAATTCAA[C/T]GTGGTCCATCCATAC | 9690 |
rs552163581 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178953 | TCTCAATGTCAGAGC[A/G]GTACTGGTGTCCCAG | 9690 |
rs552174791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259978 | CCTAAGTGCAGTGAG[A/T]TTGTTTCAAATAGGT | 9690 |
rs552205008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182765 | GGGTTGGGTGCGGGG[C/G]GGTATATAGAGTCTC | 9690 |
rs552208575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239291 | CAGCTACTCAAAATG[G/T]TATGAGTGAACGGCA | 9690 |
rs552247882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157265390 | TGTTTGTGTATACGA[A/G]GAAGGTGGAGTCACC | 9690 |
rs552265485 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229099 | GTCGAATGTACACTA[C/T]GTGCGGTTGCTTTCC | 9690 |
rs552300218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154074 | CCTGTAATCCCAGCA[C/T]CTTGGGAGGGAGGCC | 9690 |
rs552318831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157262713 | GGCATGAGCCACCGC[A/G]CCCATCCTCTTCATA | 9690 |
rs552329942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243376 | AAGAGTGCAGCACCC[A/G]TGTCCTGGTGTGGTG | 9690 |
rs552335574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259638 | CAAGACTACGTATTA[C/T]TATATGTAATTCCAC | 9690 |
rs552386655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166479 | GGCGCGATGGCTCAC[A/G]CCTGTATTCTCAGCA | 9690 |
rs552423954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157172110 | CGATCTCAGCTCACC[A/G]CAACCTCGCCTCCTG | 9690 |
rs552424050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157165955 | TTGATGCTTTTAGAA[G/T]TCAGTCTTTATCTTT | 9690 |
rs552426870 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222169 | AGCCACTGCACACTG[C/T]CTGTGAACATGTTTT | 9690 |
rs552429453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142707 | GGGGAAAGAGAGGGA[C/T]GGGGACAAGGGCTGG | 9690 |
rs552437141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160280 | GGGTTCCACCATGTA[A/G]GTCAGGCTGGTCTCG | 9690 |
rs552459377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171446 | GGGTCTCATGTTTTT[A/T]AAAAAAATCCCAAAT | 9690 |
rs552461646 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238563 | GATGGAGGTCATGCT[A/G]ACTAAGCTGGGAAAG | 9690 |
rs552487335 | snp | A/G | 9.89479e-05 | 0.00703307 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248375 | TTTTGAAGGCTCTCT[A/G]TGAGAACATGCTGGT | 9690 |
rs552490956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157142180 | TTCTCTTTGACTGCC[A/G]CATAAGTCCCTTCCC | 9690 |
rs552513999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228243 | ATGGCTGTTCCTGCA[C/G]TTGGTGCTCAGAGAG | 9690 |
rs552518435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157154457 | TGTCCTCCCCTCTCA[C/T]TTTCAGTTAAAATGA | 9690 |
rs552555639 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201508 | GCTTTCCTAGCTTGG[A/T]AACAGCACAGATTTA | 9690 |
rs552574122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197179 | TTTTCAGTATTTACT[A/G]CAGACAAATTTTCAA | 9690 |
rs552579381 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163392 | GACTCCATCTCAAAA[-/A]AAAAAAAAAAAAAGG | 9690 |
rs552581930 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232180 | CACCTGTCATTGTAT[C/T]GGGGTCTTCCCTGAT | 9690 |
rs552583633 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255904 | AGTTAGAAGGAAAGA[C/T]GATAAAATTAATTTA | 9690 |
rs552600107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190742 | AAAATTCACATTCCT[C/T]GGATTATTGATTTGT | 9690 |
rs552629061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228866 | TTTACACTCCAGGTA[C/T]GGTAACTTCAAAATT | 9690 |
rs552633502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190339 | CTTTCTGTCCCTGTT[G/T]TGGTGAACAGGCCCG | 9690 |
rs552638934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208647 | AAATTGATTAACAAC[A/G]TAAAGTAGGTCATTA | 9690 |
rs552674122 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181885 | TTATTTTCCTGCTTT[G/T]CTAAGTAACTGTCAA | 9690 |
rs552674506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196512 | CTTGTTCTGGAGAAG[A/G]CGTTCTAGGTTGAGC | 9690 |
rs552706596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243465 | GCTCAGTTATCCGTG[A/G]TAGACATCTGCTGAA | 9690 |
rs552711699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261628 | AATTAATGTAGACTT[A/G]AAGGAAGAGAATGTC | 9690 |
rs552762361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217508 | ATTACTAATACCTAC[A/C]TCTAAAGCAGATTCA | 9690 |
rs552762635 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157251112 | TAAGAAATTCACTAG[-/T]TGAAGCACCTAATTT | 9690 |
rs552865436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202408 | ACGCCTGTAATTCCA[A/G]CACTTTGGGAGGCCG | 9690 |
rs552897098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153767 | AGATGCCTTGAGCCC[A/G]GGAGTTCCAGATCAG | 9690 |
rs552907861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157243042 | CCTGGGTGAAAGAGG[A/G]AAACTCCATCTCAAA | 9690 |
rs552920836 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137041 | TCCCGGGTTCACGCC[A/T]TTCTCCTGCCTCAGC | 9690 |
rs552951562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249156 | GTTTTTAGTATATTC[A/G]TAGAGGTGTGCAGCC | 9690 |
rs552960391 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214195 | ACTTCTTTTTTCATA[A/T]TTAGGATAGGAAATA | 9690 |
rs552977023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248665 | CATTTGTGTTACAGC[A/G]TTTGACTTCCGCACA | 9690 |
rs552983402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166031 | TGTATGTAGGTGTCT[A/G]AATCTCTTGTGAGAC | 9690 |
rs553014190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259029 | TTTTGAAACGGCCAC[A/T]ATTAAATTATTACAA | 9690 |
rs553033125 | in-del | -/AC | 0.0636598 | 0.166665 | intron-variant | UBE3C | GRCh38.p7 | 7:157264298 | TGCTTGGCCTGTTAC[-/AC]ACACACACACACACA | 9690 |
rs553047785 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155553 | CATTCACTCTAGTTT[C/T]TTAACATAAAAATTT | 9690 |
rs553056159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217183 | TATTCTGAGTTATTA[A/G]TCCTCAATTTTCCTT | 9690 |
rs553058245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255644 | AATAATCTCAGCTAT[A/G]CCAGTAAATAGGTTT | 9690 |
rs553089091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172483 | TGAATTAATTACAGC[A/G]GACAAAGGAATACAT | 9690 |
rs553092904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222893 | AGGAGGGAAAGGGCA[C/T]GAAGGTGGTCGGGGG | 9690 |
rs553096627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141772 | GCATGGAGCCACTCA[C/T]CACTTGTCGTTTGTG | 9690 |
rs553098238 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157154471 | ATTTTCAGTTAAAAT[-/GA]GAGATCATATTGCTT | 9690 |
rs553101888 | snp | C/G | 0.000966962 | 0.0219669 | intron-variant | UBE3C | GRCh38.p7 | 7:157254338 | TGCTAGTTATTGTTT[C/G]TGAAAATGTTGCAGG | 9690 |
rs553127252 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157244540 | AGATTAAGTTATAAA[C/T]GTTCACTTTAGAGCT | 9690 |
rs553131364 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226402 | CTCTAATATATTAGC[A/G]GTTTTAACTTCCAAA | 9690 |
rs553135342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157161012 | GGACAGCATCCAGGA[C/T]ATGAAAGATGAAGAT | 9690 |
rs553137145 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211101 | TTTCCTCCTGTGATA[A/G]GGAAACAGGAGGAAG | 9690 |
rs553140601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248012 | TCATTTGCCGTAGCC[A/G]CCTTGGGAGACTAAC | 9690 |
rs553170464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157160574 | ATGGTACCAAGTAGT[A/G]GTTCATTATGCCGTT | 9690 |
rs553205759 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239375 | ATTTCATTTATGGAA[A/G]TTCAGAAACAAGCAA | 9690 |
rs553219950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260752 | AAACACTGGAAGATG[C/T]AGAGACTTTTGTCAG | 9690 |
rs553260128 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137368 | TCAGCCTCCCAAGCA[G/T]CTAGAAGTTTAAGAA | 9690 |
rs553290875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244069 | AACCCTGTCTCTACT[A/G]AAAATACAAAAATTT | 9690 |
rs553290975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157249668 | CATGGATCAGGACTT[C/T]ATTCCTTTTCTGGCC | 9690 |
rs553303488 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239919 | GTTGCTGCTTTCTGG[C/G/T]TGATGCAGCAGAGAG | 9690 |
rs553317577 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157193926 | CTCTCCTAACGTAAA[-/TC]TCTATTTTGGAAGAC | 9690 |
rs553321619 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143165 | AGCCACTGCGCTCAG[C/T]CTGAAATTTTTTTTT | 9690 |
rs553323775 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE3C | GRCh38.p7 | 7:157139443 | CTCGGGGCCGAGACT[C/T]GGGGCTGGATTCGGG | 9690 |
rs553328316 | snp | A/C | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174953 | TAATTAAACACAGCT[A/C]TCTGTTTGTCAAGCA | 9690 |
rs553344999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157159808 | AGCCTGGGCCAGAGC[A/G]AGACTCTGTCTCCAA | 9690 |
rs553349094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219932 | ATTGCAAGGGCCAGC[C/T]GGGTGTGGTGGCTCA | 9690 |
rs553401778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178243 | AGTTGACTTAGGACC[A/G]GAAATATATCATTGT | 9690 |
rs553425038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260263 | TACAACAGTGAGTGC[A/G]GAGAAACTGACGTAA | 9690 |
rs553435863 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157138959 | CCGCCATCTTCCCTC[C/T]CGAGGCGGCAGTTCC | 9690 |
rs553438584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177780 | TAAGCGGATAAGCCG[C/T]GTAGACACACCCCAC | 9690 |
rs553440152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144563 | TTGAGACTTAAAGAA[C/G]CTAGGGATGAATATG | 9690 |
rs553443664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190361 | ACAGGCCCGTCATCT[A/G]CTTGGTTGTCTGTAC | 9690 |
rs553461992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148194 | CCACCTCCATCTCCC[C/G]AATTCAAGTGATTCT | 9690 |
rs553470247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157222186 | TGTGAACATGTTTTT[C/T]AGTTATTGAATTTTG | 9690 |
rs553475435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177398 | GCTGTCCCGATAAAC[C/G]TGGAGCTACATCCTA | 9690 |
rs553478790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144167 | GCCGGATGCTGTGGC[C/G]CACGCCTACAATCTG | 9690 |
rs553479269 | snp | A/C/G | 6.59037e-05 | 0.00574004 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183916 | CTGGTGTATTTGCGG[A/C/G]TGCTGCAGACCTTCC | 9690 |
rs553482856 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165513 | AGCGATTCTCCTGCC[C/T]CAGCCTCCCGAGTAG | 9690 |
rs553492965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157230906 | CTCCAGCCTGGGTGA[C/T]GGAGCAAGACTCTGT | 9690 |
rs553551228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180003 | TGTTTTAAGACTAAG[C/T]GTTTGAGAATTTGTA | 9690 |
rs553553770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167227 | TGAGCCACCATGCCC[A/G]ACCTCACAGGATTTT | 9690 |
rs553559146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203892 | GCATTCAAGACACCC[A/G]GCTTACTGAGGCCTC | 9690 |
rs553581491 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172444 | TTCCTCGCTACAAAC[A/C]ATCCCTACTAGAATG | 9690 |
rs553586869 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208072 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTT]GATACATGGACTTGA | 9690 |
rs553601672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168792 | GGCAAGAGAAGGGAC[A/G]GCAGGAAACGGGGGG | 9690 |
rs553648808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157252256 | CAAATCATACAAGTA[C/T]ATCATCATTTATTAC | 9690 |
rs553666866 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157663 | CAAAAACTGAAAACA[A/C]CCTAAATGACCATTA | 9690 |
rs553687828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252948 | GGGGGTCTTGCTTTA[C/T]CTCAAACTCCTGGGC | 9690 |
rs553696533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219412 | GATGGGGCCTCTCAG[C/T]GATCGAGCATCCCAC | 9690 |
rs553696820 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157210772 | ATTGCAAACGATGAG[A/G]CCTGACTCCTTCAAC | 9690 |
rs553732106 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189393 | AATATGATTAAATAT[A/T]CACTGGCTATATTTT | 9690 |
rs553733903 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157210133 | AGTCAGCCGAGATAG[C/T]GCCACTGCACTCCAG | 9690 |
rs553739036 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244508 | TAAAGCAAGACATCA[A/T]CTCTTATATAGTTTT | 9690 |
rs553755206 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221164 | GAATCCATTCATTGG[A/T]TGAAAGACATTTGGT | 9690 |
rs553755685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180592 | TACCAAATACGCTTG[C/T]ATATGATGAGATACT | 9690 |
rs553811832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157219899 | GTGAATGAGACTCCA[C/T]CTAAAAAAAAAAAAA | 9690 |
rs553866666 | snp | A/G | 7.97925e-05 | 0.00631585 | intron-variant | UBE3C | GRCh38.p7 | 7:157187062 | AGGGGGTGCCAGCCA[A/G]AGAACATACCTTCCT | 9690 |
rs553874960 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250843 | TAAAAGCCTTCGGAC[A/G]GTGAGTGTTGTGGTG | 9690 |
rs553888792 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268926 | GAGGGGATCTAAATC[C/T]TCATTTATCTCTTCT | 9690 |
rs553895149 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157237794 | CTCATACCTGTAGTC[C/G]CAGCACTTTGGGAGG | 9690 |
rs553897540 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192698 | GGTGGATGAGAATGA[C/T]AAAATGAGCTGCCTT | 9690 |
rs553942981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241890 | TGAGAATGTTCTGCC[C/T]GGTGAGAGCAGATGC | 9690 |
rs553962709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157206775 | TTAATTTAATATATC[A/T]TAGCTCTTGATGGGT | 9690 |
rs553973771 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159971 | TCTCGTATTCTTTTG[A/T]TGTGATTATAAACAG | 9690 |
rs554018406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182520 | AGTGGAAAAGACTGA[C/T]ATATATATGTGTCTT | 9690 |
rs554021431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157242326 | AGTACCTGATGGTAA[C/T]GAAATCTGTTATCAT | 9690 |
rs554055479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188749 | AGGTTCTAGTATTTA[G/T]AAAGAGCAAGTAGGC | 9690 |
rs554071607 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242062 | ATGAAAATCTTCAGA[A/G]ATTGATTGTGGCGAT | 9690 |
rs554110248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220509 | TAAAAGTATGAAAGG[A/G]CAGCTAGCATGAGAG | 9690 |
rs554134175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213403 | CAGTGATGGCGGCAC[A/G]CCTGTGGTGGGCTTG | 9690 |
rs554145369 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157247218 | ACACGAATGGCTTTT[G/T]TAGAGGAAATTGAGA | 9690 |
rs554147092 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157219949 | GGTGTGGTGGCTCAC[A/G]CCTGTGACCCGGGCA | 9690 |
rs554147176 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145762 | TATCAATTAATAAGC[-/T]TTTTTTTTTAGAGTG | 9690 |
rs554183768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157247310 | AAACAAGATAATTAA[C/T]GTCTAACTGCATGTC | 9690 |
rs554185283 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232069 | CAGTAGCCCTTGACC[A/T]TTTTTGGCTTGTAGA | 9690 |
rs554189595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265430 | TGGCCATCAGAGGAC[C/T]GACACGCCCATAGGT | 9690 |
rs554225150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140160 | TGGTCTTGTTCCCGC[C/T]CCTCCCTTCCCACCC | 9690 |
rs554230735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259304 | ACACGTTGCATTTAA[C/T]TGGCGTGCTCTTTAG | 9690 |
rs554288158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157139453 | AGACTTGGGGCTGGA[C/T]TCGGGGCCTCCCTGG | 9690 |
rs554305208 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157214994 | GAATAGCTGACTCCA[G/T]TTTACCCTGATTAGT | 9690 |
rs554357880 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157242866 | TCTAGACCAGCCTGA[C/T]CAACATGGTGAAACC | 9690 |
rs554379327 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157141157 | GGGAGAGAGTGGCAG[G/T]AAAGAGCCCTTAGTA | 9690 |
rs554423653 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157228407 | TAACAAAGTTCCCTC[A/G]GGGCCTGGAGCTCAC | 9690 |
rs554438100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157264939 | TACCTTTTTCACTCA[A/G]CATTACATCAGGATC | 9690 |
rs554476826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259354 | CCATTTTCAAGGGGT[G/T]CAGGCAAGTTATCTT | 9690 |
rs554482656 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157247624 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9690 |
rs554487950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164977 | TTTGAACAGATAATT[C/G]TTTGTTGGGGGGAAC | 9690 |
rs554489667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140680 | CCATCTGAGACTCCA[C/T]GCCATTTACACAGCG | 9690 |
rs554492938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265464 | ATGCATTAAGTCTGC[A/G]TTGAGCAATCCCTAA | 9690 |
rs554504175 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146826 | TGGTTAATTTTTGTA[C/T]TTTTAGTAGAAACTG | 9690 |
rs554509790 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252593 | ATGAGAACCAGCAAA[C/T]GAGTCTCCTATAACC | 9690 |
rs554513480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253011 | TGCTGGGATTAGAGG[C/T]GTGAGCCACTATACC | 9690 |
rs554515701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157214295 | AATGAGAACTTAATT[A/G]TCTCATATAATTTGA | 9690 |
rs554528984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157170215 | CAATTTCCACCATTC[C/T]TGTAAACACAGCAAC | 9690 |
rs554533067 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157236366 | TCTTGCTTTAGGATA[-/T]TGATTTAATTGGGAT | 9690 |
rs554548649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157169659 | GGGATTACAAGCATA[A/T]GCCACTGCGCCTGGC | 9690 |
rs554550017 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157153057 | TGAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 9690 |
rs554557835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157207636 | AAAGTTTTAAGCTTT[C/T]TAAGTCTTTCAGTGT | 9690 |
rs554636694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146786 | CAGCATCCTGAGTAG[C/T]TGGGTGGGCATGTGC | 9690 |
rs554678238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157181358 | GGTTTGTATACCGTT[C/T]GGCTGCCTATATATT | 9690 |
rs554686650 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193254 | TTTATGGCATTAGAA[A/G]TGTCCAGTAATATTT | 9690 |
rs554689127 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157152577 | AGGGCACTTTTCGTT[G/T]ATGAGCTCATTGATC | 9690 |
rs554698480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264216 | CTGGTATTACAGGGG[C/T]GCGCCAACATGCTCG | 9690 |
rs554701897 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157266740 | ATCTTGATCCTTTTT[-/A]AAAAAATTTTTATAG | 9690 |
rs554713078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180714 | TTATGTTCACTGCCT[C/T]CCACCCAGAGTTCCT | 9690 |
rs554734539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237863 | CCATCCTAGGCATAC[A/G]TAGGGAGACCTGGTC | 9690 |
rs554774748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171218 | GCAACCTTCCCCTCC[C/T]GGGCTCAAGCAATCG | 9690 |
rs554805920 | snp | A/G | 0.000162562 | 0.00901413 | intron-variant | UBE3C | GRCh38.p7 | 7:157164395 | CTATGGCCTCATGCA[A/G]TCGCCTCCCTCATTT | 9690 |
rs554811502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176831 | GGGGCTGTTTTCTCT[A/G]AGGAGCACTGATTCT | 9690 |
rs554823034 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157216353 | TTCCAGATTCGTGGG[G/T]TTTTTTTTTTTTAAT | 9690 |
rs554833099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254927 | GTCCCAGCGTGGTGG[C/T]GTACACCTGCAGTCC | 9690 |
rs554868741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260044 | ATAATAAAGACGTAT[A/G]AACTTAAACGTGTTA | 9690 |
rs554869809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248698 | TTAGTTAGAATGACT[A/G]TGGCTGTGAGTTAGA | 9690 |
rs554897617 | snp | C/T | 0.000910731 | 0.0213198 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267771 | AGCTGATGCTGGGGT[C/T]AGACCCCTACAGAGA | 9690 |
rs554958030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146168 | CACCATTTCTGAAAA[C/G]ACATTCCCCAACTCC | 9690 |
rs554973340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182849 | CGCCTCCCGGGTTCA[A/G]GTGATTCTCCTGCCT | 9690 |
rs554974968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227304 | GAGCTCCGAGGGCAC[A/G]GGTGCTGTGGTCAGG | 9690 |
rs554989725 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149998 | CTTCGATGGTGGTCA[A/G]ATTACAGGCTGTAAT | 9690 |
rs554992202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157184952 | AGTGAAGCCGTTTTT[A/G]TAGTGGACAGTGGAT | 9690 |
rs555074180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149378 | CAACCGATTTTTAAA[A/G]ATAGAAACCAAGCGG | 9690 |
rs555079453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195319 | GCAGAAACACCACTA[A/T]TTTTAACAGAATGCT | 9690 |
rs555083824 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157162005 | AAACCGGGAGGCAGA[A/G]GTTGCAGTGAGCCAA | 9690 |
rs555093037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232288 | TGAATTTGTCTTTTG[A/G]GGGGACACAGCTCTA | 9690 |
rs555120041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201963 | AGTTGCACAAAAAGA[A/G]AAATCAGTGTCTAAT | 9690 |
rs555177832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157179762 | ACGGACTTGAAGTCT[C/G]GACCACTTGGTCCTC | 9690 |
rs555224130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141643 | CGGTGTATATGTGGT[C/T]TGTTGTCGACAGACT | 9690 |
rs555237978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211846 | CCTGCAGTATCACCA[C/T]GTAGTGAAGGAGACA | 9690 |
rs555243013 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248147 | GCTCCTAGGTGGTCT[A/C/G]TTCCAGAGTTCTCTG | 9690 |
rs555253506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185532 | TGAGCCAGGCACTCA[C/T]AGGTTTCACTGCAAG | 9690 |
rs555273185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254421 | TTTTTTTTTCAGACT[G/T]AGTTTCACTCTTGTC | 9690 |
rs555289915 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | UBE3C | GRCh38.p7 | 7:157210379 | CCCAAAATAAAAATC[-/A]ACTGCATAATTTTTG | 9690 |
rs555295216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157199282 | CTTACTCTTTTTTCC[A/G]TATGACTGTTGCGTA | 9690 |
rs555295585 | in-del | -/A | 0.347694 | 0.230122 | intron-variant | UBE3C | GRCh38.p7 | 7:157219902 | AATGAGACTCCATCT[-/A]AAAAAAAAAAAAAAA | 9690 |
rs555310752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173703 | TCCAACAGTCCTATT[A/G]TATAATGTATAGTTA | 9690 |
rs555363990 | in-del | -/TA | 0.000251461 | 0.0112101 | splice-donor-variant | UBE3C | GRCh38.p7 | 7:157225540 | TTCTCCAGAAAATGG[-/TA]TATATATAATTCTTT | 9690 |
rs555370167 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164797 | GACAAGGTTCCTGCC[A/G]TGAACCAGGATGCTG | 9690 |
rs555377686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229767 | TTACAGGCACATACC[A/G]CCATGCCCAGCTTTT | 9690 |
rs555381331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191525 | CGAACACCTGGGCCC[A/T]AGTAATCTGCTTGTC | 9690 |
rs555434115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157205472 | TCGGGGATAACAGTG[A/G]AAAGCAGGCTCATCA | 9690 |
rs555463874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236066 | AGAGGTCTTCAAGAG[A/T]GATCCTGCAGAGGAA | 9690 |
rs555467315 | in-del | -/TAAT | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157145396 | GGTGACAGGTGCCTG[-/TAAT]TGCAGCTACTCAGGA | 9690 |
rs555488928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240247 | TTTTGTAGAGATGGG[G/T]TTTCGCCATGTTGGC | 9690 |
rs555497075 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268858 | TCTACAAACAGAAAG[C/T]GTTTCAAAGCGTCAG | 9690 |
rs555500883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168638 | GAATGAAGTTCTCAC[A/G]TATGCTGTAACATAG | 9690 |
rs555501594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257340 | ATTAATAATGTCTCA[C/T]AAATCTGTAACACAT | 9690 |
rs555514878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204682 | CCAGTTTAGTTTCCT[C/T]CTTCTTGAAGATGAG | 9690 |
rs555521278 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174758 | TGGAAAATGCACATA[A/C]CTCTAAATAAAACCG | 9690 |
rs555551685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230987 | GTCCCTAAGATCCTC[A/C]CACCCCTTCCTTAAG | 9690 |
rs555571232 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138657 | CTCGCCGCGCTCCCC[A/C]AGCACGCACCAGGCC | 9690 |
rs555604021 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224521 | ATAAAAAAAGAAATG[G/T]ACAAATATCTTAATT | 9690 |
rs555604064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251463 | GACTTGAGTCACGAC[A/G]CCTTGGTTCAGGTCC | 9690 |
rs555621291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252033 | CCCAGCTACTCGGGA[A/G]GCTGAAGCACAAGAA | 9690 |
rs555645009 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157182818 | CAGTGGCTCCATCTC[A/G]GCTCACTGCAACCTC | 9690 |
rs555646733 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141569 | TTCATGCAATGGTGA[A/G]TGTCTGTGCATCCAA | 9690 |
rs555656012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231402 | TATGTGTGGTTGTTA[C/T]CCAGGTTTACCATAA | 9690 |
rs555657203 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184443 | CTTAAAAATTACTTT[C/G]AAGTTCTTATCTCTT | 9690 |
rs555664801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143434 | AGATAGCAGGTATCA[C/T]CACCACAGGAGTTGC | 9690 |
rs555689452 | in-del | -/A | 0.425123 | 0.178415 | intron-variant | UBE3C | GRCh38.p7 | 7:157156714 | AATTCCCTTCTTTTT[-/A]AAAAAAAAAAAAAAA | 9690 |
rs555689599 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138044 | AATTGGTTTCAATCG[C/T]GTATGATATATATGT | 9690 |
rs555699320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262960 | ACCTTTTCTATTTTT[A/T]AAATTTTTTTGAACA | 9690 |
rs555715206 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145962 | ATGGATCTTGCTTCT[C/T]GCGTTGTGTCTAAAA | 9690 |
rs555726353 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157171072 | CCTCCCTGGCCTCTC[-/A]AAAGTGCTGGAATTA | 9690 |
rs555781467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163462 | GTTTCCTCTGGGGTA[A/G]TATTTTACAAAGCTA | 9690 |
rs555791050 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186618 | TCATAGGCAAAAACC[A/G]GGTATTCAGAGTTTA | 9690 |
rs555792130 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168147 | ATGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 9690 |
rs555812408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157190914 | GTGTTTCGTGCCCCT[C/T]TCCTTTTGCGTATGC | 9690 |
rs555818437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162999 | TCAAAACTTAGTTTT[A/G]TTTATGAAAAAAAAT | 9690 |
rs555860131 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157212456 | TATACATTTGTGATA[A/G]TATAGCTAGTGCGTA | 9690 |
rs555889377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156348 | GTCCTGCTCTGTCAC[C/G]TGGGCTGGAGTGCAG | 9690 |
rs555896533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157143506 | CTCCTTCATTCCTGG[C/T]TCTGCAGACTGGCTT | 9690 |
rs555898740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144638 | TTTTTGTAGATCTGA[C/G]AATAGTGGGAGTAGA | 9690 |
rs555903530 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249749 | GACATTTGGGTTGTT[-/C]CTATGTTTGGGCTAA | 9690 |
rs555936419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168742 | GTCCAGAATAAGCAC[A/T]TCCATAAGATAGAAG | 9690 |
rs555953619 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157185674 | CAAAGTTCACCCTTG[A/C]TAAGCTCTTTTGCCT | 9690 |
rs555956599 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157168179 | ACATGGTGAAACCCC[A/G]TCTCTACTAAATATA | 9690 |
rs555967287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152046 | TTCTTAGGACTATTT[A/C]CATATTAACATTACT | 9690 |
rs555970252 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267821 | GCAGCGCCTCCCCAG[A/T]CCCACGAGGATACTC | 9690 |
rs555972762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157187124 | CTGCTCTTTTCTGGT[A/G]GAGATTGATGTAGGA | 9690 |
rs555982509 | in-del | -/AGAGATGTGGTAACAGAAGGGTCAT | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157196092 | CCAGGGTGGTGTCAG[-/AGAGATGTGGTAACAGAAGGGTCAT]AGAGATGAAACAGTG | 9690 |
rs555982670 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189412 | TGGCTATATTTTAAG[C/G]GGGCAAAAAATAAAG | 9690 |
rs556005063 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157193085 | GTGTCTAAGGCTTAC[C/T]TCCTACTCTTAGCTC | 9690 |
rs556031395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229837 | AGGCTGGTCTTGGAC[C/T]CCTGGCCTCAGGCAG | 9690 |
rs556036273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257470 | GTTGATCTTACGTAA[C/T]TTGGCTTATTTTTAG | 9690 |
rs556051394 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213601 | GTGATTCTGAAAGTG[A/C]ATGTGGAAAAAAGGA | 9690 |
rs556066675 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157258109 | TGTACCACCATGCCT[G/T]GCTGACATTTTGATT | 9690 |
rs556076784 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269313 | GCTATTCTGAGCTTA[C/T]TTATTTATTTGTATG | 9690 |
rs556097541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144126 | TTGGAGAGTGAATGG[G/T]AAGTCACAAACAGGG | 9690 |
rs556108698 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268944 | ATTTATCTCTTCTAT[A/G]TCTCGTATTTTACTG | 9690 |
rs556117952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179880 | TTTGTTGAAAACTTA[A/G]GGAAACAGTATTCCG | 9690 |
rs556136980 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210316 | GATTTCTGTTCTTTG[A/G]TCACCTGTCCCCCAA | 9690 |
rs556154078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180481 | TCTAATGATAAAGTA[A/C]TGAGTATGCATTGTT | 9690 |
rs556155040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186351 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9690 |
rs556163969 | snp | A/G | 0.00165279 | 0.0286996 | intron-variant | UBE3C | GRCh38.p7 | 7:157139390 | GCCTGCGCGGCCGGG[A/G]CTCGGGGCTGGGACT | 9690 |
rs556183130 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228091 | TAATCAACTAATGTG[A/T]TTATTCCACGTGTCA | 9690 |
rs556185077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193269 | GTGTCCAGTAATATT[G/T]TTTTAAAAAGAAAAA | 9690 |
rs556217520 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157251589 | GAAGTAGGTCATGTA[C/T]GGTGGTGTCTTGTGG | 9690 |
rs556260271 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213962 | AAAATGTATTATTTG[A/T]TATAAATAAATATAA | 9690 |
rs556268563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157681 | TAAATGACCATTAAA[A/G]TATAACATGGTGGCT | 9690 |
rs556281975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213296 | CATATAACTTACCAC[A/G]CTGGTTCTCAAGTCG | 9690 |
rs556290349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252159 | AAAAAGTTATAGAAA[C/T]GTCAGTTTTCTCTGA | 9690 |
rs556307005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157164203 | CTTGCTCTGTGACCC[A/G]GGCTGGAGTGCAGTG | 9690 |
rs556329026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246789 | TTCTTTCTCTAAAAC[G/T]GTTCTCCACCTGTTC | 9690 |
rs556329596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200720 | GCTCACTGCAGCCTT[A/G]AACTCCTGGGCTCTA | 9690 |
rs556425824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157247079 | TTTATTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 9690 |
rs556441200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157264873 | CACTGCTCCTGGTCA[C/T]GTAATTTTTAAATAT | 9690 |
rs556442784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157145718 | GCTCTTTTCATGGCT[C/T]GACAGTTCATTTCTT | 9690 |
rs556446332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157196133 | GAGATGAAACAGTGC[C/T]GGTTTTTAAGATAGA | 9690 |
rs556448089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193976 | CAGTTGTTTTTGTAT[G/T]TGCATCTATAGGCAC | 9690 |
rs556449458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226461 | CATGTTGGTCAATGC[C/T]GAGGGGATTAAAATG | 9690 |
rs556481526 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169813 | AGCCTCCTGAGTAGC[G/T]GGGACTACAGGTGCA | 9690 |
rs556543861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157116 | GGCTCACACTAGTAA[A/G]TGTCAGCTTCTGAAA | 9690 |
rs556577503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241781 | CCATCAGCTGACAAA[C/T]GGGTAAACAGAATAC | 9690 |
rs556579660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237237 | ACCAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 9690 |
rs556580724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163633 | ATTATATCTAGTGAC[C/T]TCTGGGAAACCATTT | 9690 |
rs556583163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196177 | AGGAATGCGGATGTT[C/G]TCTAGAAGGTGGAAT | 9690 |
rs556659975 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149464 | ATTAAATCTGGGCCT[A/G]CAGGGAGGTGAGTAA | 9690 |
rs556668655 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140172 | CGCCCCTCCCTTCCC[A/T]CCCCTTCCCATCATT | 9690 |
rs556673204 | snp | A/G | | | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220716 | TATGTGCCAGCATCC[A/G]GACATGTGTGGAGGT | 9690 |
rs556686400 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261170 | AATCAGCCGGGCATG[A/G]TGGTGCATGCCTGTA | 9690 |
rs556706336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159934 | AGAGCCTAATCTTCC[C/T]CTTAAACTAAGCAGC | 9690 |
rs556733769 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144349 | TTTTTTGAAAAGCAC[C/G]GGAAGATTGGATGAT | 9690 |
rs556783129 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157187817 | TCCTGACCTTGTGAT[C/T]CGCCTGCCTCGGCCT | 9690 |
rs556800348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157209470 | TTTCTTAAAGATTGA[C/G]AAATTTGCAATTTTT | 9690 |
rs556806235 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157145258 | AAAAAAAGAAAAAAG[A/G]AGGAGGCCCGGCACT | 9690 |
rs556832838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142399 | AGAAGTTGATAATCT[C/T]GTTGGGCAGATAAGA | 9690 |
rs556840250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264262 | ACACACACACACCTG[C/G]TACTACAGGTGTAAG | 9690 |
rs556847111 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157192286 | TACCACGTTTTTAAA[G/T]TTTTCTTTTAAGCTT | 9690 |
rs556855886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196740 | TTGGGAGTCTGAGGT[A/G]GGTGGATCACCTGAG | 9690 |
rs556860456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231474 | GCACTGCACGAAACA[A/C]ATTTGTATGGTTGTA | 9690 |
rs556896200 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155824 | AGCAGTTGGCTGTGC[C/T]CACTGTGGATTTCAC | 9690 |
rs556897112 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157217955 | TTGTGCCCTGGAGGC[A/G]GAGGTTGCAGTGAGC | 9690 |
rs556936066 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157166570 | ACATGAAGAAACCCC[A/G]TCTCTACTAAAAATA | 9690 |
rs556941935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244670 | CTGTGATGTGGTTCA[C/T]ATTTATTCTGATAGA | 9690 |
rs556957694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190384 | GTCTGTACCTGCAGC[C/G]TGAAACTGCAGTGTC | 9690 |
rs556973182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243957 | AGGTATGTTGCCAGG[C/T]GCGGTGGCTCACACC | 9690 |
rs557010375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209954 | GGGAGGCCAAGGCGG[G/T]TGGATCACGAGGTCA | 9690 |
rs557011867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239427 | GGCAGGATCCTGATG[C/T]TCCTGGGAGGGTAAC | 9690 |
rs557033960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217620 | CGGGCAGATCACTTA[A/C]AGCCAGGAGTTTGAG | 9690 |
rs557039543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157249761 | GTTCCTATGTTTGGG[C/T]TAATAAGAATATTAC | 9690 |
rs557057718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248937 | TCCTCACTCCTTGCC[C/T]GCTCAGAGCCACCTC | 9690 |
rs557070641 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157223572 | CAACTGATTGAAAGC[C/G]AGTAAACACTATAGA | 9690 |
rs557073789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167264 | ACCATTTCAAGCCCA[A/G]GAACTACATCTACAT | 9690 |
rs557113363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240275 | GGCCAGGCTGGTCTC[A/G]AATTCCTGGCCTCAA | 9690 |
rs557134728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243525 | TAGAGATTGGCTTTA[A/G]GGCACCTGCCAGTGG | 9690 |
rs557148530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240686 | GAGAGGAAATTAATC[C/T]GTGAATGGAGATTTG | 9690 |
rs557202052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148327 | ATACTGGCCTTGAAC[C/T]CCTGGCCTCAAGTGA | 9690 |
rs557206220 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182000 | ACTTGGCTAATTTAG[A/G]AGAGTAGATTATCCT | 9690 |
rs557216677 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137061 | CCTGCCTCAGCCTCC[C/G]AAGTAGCTGGGACTA | 9690 |
rs557273001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157245521 | TGACTTTTCAACACA[A/G]CTTTCTTTACATTAT | 9690 |
rs557308138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266622 | TCTAATTACATAATT[A/G]TATAATTTATTAGCT | 9690 |
rs557331147 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157250570 | TCAAGTGATCCTCCT[G/T]CCTCAGCCTCCCAAA | 9690 |
rs557331641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157161086 | CTAAATATAATGTGG[A/G]GTCCTGGATAGGATT | 9690 |
rs557359583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256695 | TAGTGTCACAGCCAT[A/T]TACACAGCCTCGGCA | 9690 |
rs557370969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190466 | ACAGACTCAGGTCCT[C/T]GGCTACCAAAGCCAC | 9690 |
rs557415979 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157263340 | ACAGAGAATCCGTGC[C/T]CTTTTGTGCCGTGTC | 9690 |
rs557433160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242867 | CTAGACCAGCCTGAC[C/T]AACATGGTGAAACCC | 9690 |
rs557435978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157184617 | TGAGGTATGGCTATC[A/G]TAAGTTGTTATTTTT | 9690 |
rs557460908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178270 | TTGTTCTATTTGGGG[G/T]ATATTGCAGGCGTGG | 9690 |
rs557479739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157261252 | TGGAGGTTGCAGTGA[A/T]CCAAGATTGCACCAT | 9690 |
rs557496415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217696 | ACAAAAATCAGCCGG[A/G]CGTGGTGGCAGACGC | 9690 |
rs557559246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157185394 | TTTTTAATACATAAG[C/G]GTTTCAAGGTCTGTG | 9690 |
rs557590323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202903 | TTTTCTTTTTAGGAA[C/T]AAGAAGTTAGAAGAA | 9690 |
rs557595888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184790 | GAGCTTCACTAGTAT[C/G]GAATGAAAGAGATCA | 9690 |
rs557606539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160468 | CTGTTTTTCTGTTTA[A/G]TGATGAAAGATTTCC | 9690 |
rs557617416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204783 | TGCCCAGATGTCTTC[A/T]GTGTGGGCAGTAGGT | 9690 |
rs557643400 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137651 | CTCACTGCAACCTCT[G/T]CCTCCTGGGTTCAAG | 9690 |
rs557685024 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245486 | AATAGTATTAACCAT[A/C]CTTAACTTTAAACAA | 9690 |
rs557696428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178340 | TTAAAGAGATTCGTA[C/T]CTGAGTTTAATTAAA | 9690 |
rs557737564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160956 | TCCTTATTTCGTAAC[C/T]TTACTGTAATCATGA | 9690 |
rs557750954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148369 | CAGCTTCCCAATGTG[C/T]TGGGATTACAGGTGT | 9690 |
rs557766746 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157186566 | AAGTAGGAAATGAAG[-/T]TTTTTTTGAAATGTA | 9690 |
rs557780697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197441 | AATCCAGATTTGTCT[A/G]TATTCAGGTTGGAAG | 9690 |
rs557794847 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225901 | GCTGCAGTCGAACTC[-/T]TGATTGTGCTACTGC | 9690 |
rs557819623 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204826 | TGTTTGATAAATAAT[C/G]TCAAAACAGTCTACA | 9690 |
rs557820688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211752 | CTCAGTTATTTGAAC[A/G]CTCACAGTATTCATC | 9690 |
rs557870932 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241472 | CGTGCAAAGATGGCC[A/G]GCATCACTAGTCATC | 9690 |
rs557901497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223932 | CTCAAAGGGGGGAAG[A/G]AACTTTGCATTGTTT | 9690 |
rs557923452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178957 | AATGTCAGAGCGGTA[C/T]TGGTGTCCCAGACGC | 9690 |
rs557934928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143388 | TGAAAGGATAGGCGT[A/G]TCTGACAGAATAGAA | 9690 |
rs557945879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236032 | TATGTTAGTGATTGT[C/T]TACTGTGATAAAGTG | 9690 |
rs558006826 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157153881 | CCTGTGGTTTCAGTT[-/A]ACTCGGGAGGCTGAG | 9690 |
rs558070313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157142839 | GGTACCCCCTAACTC[C/T]AAAATAAAAGTTGAA | 9690 |
rs558082258 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184114 | CCACCCGTAGTTTCA[A/G]TTACACAAGTCAGAC | 9690 |
rs558091722 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210050 | CTGGGCGTGATGTAC[A/G]CCTGTAATCCCAGCT | 9690 |
rs558114173 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268587 | GTTTGAACCAAAGTG[G/T]CGGCTGCATCTTTGT | 9690 |
rs558164289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162285 | CTGCAAGCTCCACTG[C/T]CTGGGTTCAAGCGAT | 9690 |
rs558164302 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157168084 | TAGCCGGGCACGGTG[C/G]CTCATGCCTGTAATC | 9690 |
rs558183956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173528 | GCAAAAATCAACATA[C/T]ATGGCTATTTCTTCC | 9690 |
rs558196703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167697 | ACCCGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 9690 |
rs558241407 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171393 | TCATCCTCCCAAAGT[C/G]GTAGAATTATAAGCA | 9690 |
rs558243465 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138309 | TGTGTACATGATACA[C/T]ATTTATATGTATTGA | 9690 |
rs558262416 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245773 | TTAAAAAACAGCATT[C/G]TTCAGTCAGGAGTTC | 9690 |
rs558262909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220610 | GAGAAATGTCCAGCA[A/C]CAATTCTGTTCAAGT | 9690 |
rs558282762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256766 | GCACAGCACGTACAC[A/G]GGTGATACACACATG | 9690 |
rs558294733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150685 | CTTGTATTTATGAAC[A/G]TGATTTATTGTTAAT | 9690 |
rs558348713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238425 | CTGCTGCCCATGTCC[C/T]GGTGGTAGTGCTGGT | 9690 |
rs558350240 | in-del | -/CCTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187075 | CAGAGAACATACCTT[-/CCTC]CCTGGGAATTGCTCT | 9690 |
rs558352663 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195799 | AATGGGTTGTGACTT[C/T]TGAGCACCTATGAGT | 9690 |
rs558388926 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207259 | CCATGGTGACTTTAC[C/T]TTGCCTTTAAATAGT | 9690 |
rs558414720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199240 | TTTCAAATTATTTTG[A/G]AAGTTCGTATTTTTC | 9690 |
rs558439235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192394 | CATAAAAACCCTTAC[A/G]GGGAAGACCATCACC | 9690 |
rs558447764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205409 | CTGATGATGTGTTGG[C/T]GGTGATGATTCTTGT | 9690 |
rs558474506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240744 | AGACCTGTGGAGTCG[A/C]GGTCCTTCAGGGAGT | 9690 |
rs558475293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159006 | GGATATTAAGTCCGT[C/T]ATCAATAGAGTGTGA | 9690 |
rs558490742 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207754 | CTTTAGAAGAGCTGA[A/T]AATGTTGTCTCGATG | 9690 |
rs558503024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157165061 | TGCCAGTAGCACTCC[A/G]TTACCTCAGTTGTGA | 9690 |
rs558530763 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157242641 | GGTTTGCTACTTTAG[C/T]GAACTTCCTTGTTCA | 9690 |
rs558557817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157254216 | TAAAATTTACCTCAA[A/G]TGTTATTATTTGAAC | 9690 |
rs558558295 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157202024 | GAGAGTATGGTTTTA[C/T]CTGAAGGTAAGTTTC | 9690 |
rs558565789 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157171017 | AGGTCTTGCTATGTT[G/T]CCCAGGCTGGTCGTG | 9690 |
rs558602942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208522 | TGCATCTTTTCTATG[C/T]GGCCCTAACTACTTA | 9690 |
rs558603580 | snp | A/G | 9.0164e-05 | 0.00671371 | intron-variant | UBE3C | GRCh38.p7 | 7:157170265 | ATTGTGTGTCCAAAT[A/G]CTATATTTATGGGTC | 9690 |
rs558611279 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217322 | ACCTAATTTTTGTGA[-/T]TTTTTTTTTTTTGAG | 9690 |
rs558623532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242978 | GAAAATCGCTTGAAA[C/T]CGGAAGGCAGAGATT | 9690 |
rs558652060 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157222015 | GTTGTGACCACAGGC[A/G]TGTGCCACCACACCT | 9690 |
rs558672779 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157177339 | ACTTCATTTTTTAAG[A/G]TGGGTTGTCTCTTGA | 9690 |
rs558689087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227695 | CAGAGTGAGACTTCA[A/T]CTCAGAAAAAAAAAA | 9690 |
rs558711426 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240377 | TGTGAATAGGCTTCA[A/G]TTAATAAGTGTGACT | 9690 |
rs558740033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166343 | TAGTTGATTCTTTTT[A/C]AAAATACTTACTCTT | 9690 |
rs558781238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171851 | AGCTGGGATTACAGA[C/T]GTGTACCACCACGCC | 9690 |
rs558818770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254970 | GTACACCTGCAGTCC[C/T]GGCGTGGTGGCGTAC | 9690 |
rs558823068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260726 | GAAGTTTGGAGGACC[C/T]GCTCCCATCAAAACA | 9690 |
rs558835794 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157201377 | TAGTAATTATAATAT[G/T]GTGATATATTAATAC | 9690 |
rs558836790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157195444 | TCACAAGCCCAGAGA[A/C]CTGAGCAGTGAGCTG | 9690 |
rs558841336 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157208249 | CAGCTAATTTATTAG[-/T]TTTTTTTGTAGAGAC | 9690 |
rs558888461 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196262 | AGCACCGCGAAACCC[A/G]TTTGGACTCCTAACC | 9690 |
rs558901620 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157147152 | TGACAGTGTTGAGCC[G/T]TCCTATCCATGAATA | 9690 |
rs558911885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232506 | AGGTGTGCACCACCA[C/T]GCCCAGCTAATTTTT | 9690 |
rs558931953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165477 | ATCTCAGCTCACTGC[A/G]ACCTCCGCCTTCCAG | 9690 |
rs558997055 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157141386 | TGACTTAAAGAGGGG[A/G]ACGCTGTCACTAGTC | 9690 |
rs559039157 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157195068 | TGATGAAGGTATGGC[C/T]GTATAACCTTCTGCT | 9690 |
rs559041361 | in-del | -/TG | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139964 | CAGCCTCCTGGAAAC[-/TG]TGGAGAGACTCCGGA | 9690 |
rs559057367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153690 | GCGTTTCTACTCTGC[A/C]GTCAGTGGCCTTTTT | 9690 |
rs559066448 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157152706 | TGTGGTTTGTTTATC[C/T]GGATGCTGTACGGCC | 9690 |
rs559168891 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227412 | AACTTTAAAACTACT[C/T]CCTGGGCGTGGCGCA | 9690 |
rs559189082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157144220 | AGGATCGCTGGATCC[C/T]GGGAGTTCAAGGCTG | 9690 |
rs559235941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222801 | ATACTGCCTGGGGCC[C/T]ACTGTGTATACAGCC | 9690 |
rs559285622 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176484 | TTTGCCATGTTGGCC[A/G]GGCTGGTCTCAAACT | 9690 |
rs559287996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248818 | GGCAGCCCCTCCTGC[A/G]GAGCTCCACTCTCGA | 9690 |
rs559290239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217032 | TCAGCTTGTGTCTTT[C/G]TGGAGAGAAGAATTA | 9690 |
rs559313851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239312 | GTGAACGGCACAGAC[C/T]TAACATTGAGTTGAA | 9690 |
rs559388040 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262736 | TCTTCATAGCATTTT[A/G]TGGGCTGTGCTCTTA | 9690 |
rs559391411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194467 | ATAAAAGACTTTTCT[A/G]GGTACTTAGAATGCT | 9690 |
rs559428483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157201003 | AAAGTGACTTGAGTC[C/T]GTCACTAAATATTTT | 9690 |
rs559431450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146370 | CCGAGTAGCTAGGAT[G/T]ACAGGTGTGCACCAC | 9690 |
rs559489256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247656 | GAGATCGCGCGGCTG[C/T]ACTCCAGCCTGGGCA | 9690 |
rs559495509 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236788 | CCAGGCTGGAGTGCA[A/G]TGGTGCGATCTTGGC | 9690 |
rs559504144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157146986 | GTAGTGTGAGTCCTT[C/T]GACTTCCTTCTTCTT | 9690 |
rs559507462 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157267354 | TTGAACCTGGGAGGC[-/A]GAGGTTGCAGTGAGC | 9690 |
rs559566033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157240890 | GTAGAATGACAGTCA[A/G]CTGTGTGCTACAGAT | 9690 |
rs559578007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157160062 | TTTTTATGTAATTCC[A/G]TAGTTACTTTTTTTT | 9690 |
rs559582966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189517 | TTTCATCTGGCATAC[A/G]TGGGGTTTTTAGTGG | 9690 |
rs559603869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176948 | CCACGTGCCAGAACA[C/T]TGAATTTTTCTTTTT | 9690 |
rs559611401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259550 | GATATTTAGAATTTA[A/G]AAGGAATAAATGATA | 9690 |
rs559621854 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221270 | TTTGTTTGACATGGA[A/G]TAAGTTTCACTGGGA | 9690 |
rs559625102 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258620 | GTGCGCCTCCATGCC[C/T]GGCTAATTTTTGTAT | 9690 |
rs559633219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216056 | ATGACATAGTGAAGT[A/G]TGTCCAGGCCAGCCT | 9690 |
rs559633883 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157183107 | GAGCAGAAATGTGGG[G/T]TTTTTTTTCCCACAC | 9690 |
rs559649629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190264 | CCCTGGGGACCTCTC[C/G]TCTGTCCCCTCCCAG | 9690 |
rs559672065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182693 | CATACATACATACAT[A/C]CATGCATGAATTATT | 9690 |
rs559675027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157147896 | ATAAATCCCACTTGA[C/T]TGTGATGCATAATTC | 9690 |
rs559702729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265583 | TGCCCAGCAACACGT[C/G]GTGCCGCGCGTGTGC | 9690 |
rs559707761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168294 | AGGCGGAGCTTGCAG[C/T]GAGCTGAGATCAAGT | 9690 |
rs559708167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157162472 | TGCTGGGATTACAGG[C/G]GTGAGCCACCGTGCC | 9690 |
rs559715826 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153983 | GCTTGGGTGACAGAG[C/G/T]GAGGCCCTGTCTGGG | 9690 |
rs559721531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233845 | TTTCAGTGACTCCAC[A/G]TCGTTGTCAGCACTT | 9690 |
rs559743903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167915 | AACAATGATGAAGAA[C/T]GCATATTTTTGCCAG | 9690 |
rs559752333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209638 | AGCTTTCCATGATGT[A/G]CAATATCAGGTGTTG | 9690 |
rs559752377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202288 | AGTATGTAATAGGTA[A/G]GAATTTCATACTTAA | 9690 |
rs559787636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157196261 | AAGCACCGCGAAACC[C/T]GTTTGGACTCCTAAC | 9690 |
rs559788183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209029 | GTCAAGCTATCTATT[C/T]AATTGAAAGAAGTTA | 9690 |
rs559834499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157239212 | TACAAAAATGTCCTT[C/T]GAAAGCATAATGATA | 9690 |
rs559839095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257541 | GGAGTTCGAGACCAG[C/G]CTGGTCAACATGATG | 9690 |
rs559856545 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245945 | GCAGTGAGCCGAGAT[A/C/T]GTGCCACTGCACACT | 9690 |
rs559873407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239609 | TACAAGAGGAAGGAT[C/G]GGAGAAGAATTGGGG | 9690 |
rs559875638 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157200753 | GATTCTCCTACCTCA[A/G]CCTCATGAGTAGCTG | 9690 |
rs559921416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174306 | AGAAATACCGTATTT[A/C]TCATATATTTTTATT | 9690 |
rs559958037 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268716 | TGCTTGGCACCCTCT[G/T]CTTCCTGGTGCTGCT | 9690 |
rs559984008 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234286 | ACCTGTATGTTCTTC[G/T]GACGGTGTTGTAGTT | 9690 |
rs560062937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157241458 | ATGGGCCATTGGTTC[A/G]TGCAAAGATGGCCAG | 9690 |
rs560071446 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211766 | CACTCACAGTATTCA[G/T]CCCACCCATAGTGAC | 9690 |
rs560117753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202590 | TAAACCTGGAAGGCG[A/G]AGGTTGCAGTGAGTC | 9690 |
rs560128240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157256034 | CGTCTGTTCAGCGGC[A/G]GCTTTGAACTGCAGC | 9690 |
rs560157583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173862 | AGAAAGCCTGTGTGT[A/T]GGCAAATTAACTAAT | 9690 |
rs560164174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180950 | GCCTCCTAAAGCCCA[C/T]CCCGGGGCCCCAGGT | 9690 |
rs560194567 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157180234 | TGCACATTCTGTGCC[A/C]TGAAGCTTTTTAACA | 9690 |
rs560199336 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222507 | CACTGCAGCCTTGAA[A/C]TCTGCAGTCTCAGGC | 9690 |
rs560236976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218275 | ACATGGTCAAACCCA[G/T]TCTCTACTAAAATAA | 9690 |
rs560240627 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157264398 | GTGAGTCAACATGCT[A/C]GGCCTGTTACACACA | 9690 |
rs560259976 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225715 | GCACTTTGGGAGGCT[A/G]AGGTGAGAGGATTGC | 9690 |
rs560277813 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188328 | AAGTAAGGAACCCAT[C/T]GGTTGAAATGGCCTT | 9690 |
rs560281237 | snp | C/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207462 | TTTGAAGATTCTAGT[C/G]GAATCATCCCACTCT | 9690 |
rs560312233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156592 | GTTACAGGCATGAGC[A/C]CCGCATCCGGCCCCA | 9690 |
rs560365229 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209427 | TAAGTAAACTGGGAC[A/G]GTCACATGGTAAGCC | 9690 |
rs560378171 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157230739 | GTTTTAAGAATTTAG[C/G]TATCTGTATTGGGCC | 9690 |
rs560397100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157193334 | GTGCTATAAGAGTTC[A/G]ACAGATCATTGGGTG | 9690 |
rs560427759 | in-del | -/GTTA | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157189809 | CAGTTTTTTAGGGTT[-/GTTA]GTTTGTGACGGAGTC | 9690 |
rs560449009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258530 | AATGGCGTGATTTCC[A/G]CTCACTGCAACCTCT | 9690 |
rs560455688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157213871 | AATCACAATTACTTT[A/G]AAAAATGTAGTTATG | 9690 |
rs560471977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205751 | CACAACTGCAAACAT[A/G]GATCATGTATGCTCA | 9690 |
rs560480159 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157139618 | TCGAGGCCGCGCCCG[G/T]GGGGGCCTTGCCTGT | 9690 |
rs560495541 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169182 | CTTATTTTAAATATG[G/T]TATCTTTGTACACCT | 9690 |
rs560548357 | snp | A/G | 4.9652e-05 | 0.00498232 | intron-variant | UBE3C | GRCh38.p7 | 7:157225377 | AGGTCTTTTGTTTCT[A/G]ATAACCTTACAGCTT | 9690 |
rs560555524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241491 | TCACTAGTCATCAAG[A/G]AAGGGCAAAGCATAG | 9690 |
rs560561058 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201563 | GTCTCATCAAATGGC[C/T]GGTTGTCTGAGGCAG | 9690 |
rs560602267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154638 | GTCTTTAGAGTTTTG[C/T]TATTAAAATAGTGCC | 9690 |
rs560649893 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215222 | CTCTGTCCACGGGTA[G/T]GTCATTCAAGGGGTG | 9690 |
rs560651451 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157263679 | AAAAAAAAAAAAAAA[A/G]GTCTAGCAAGTATTA | 9690 |
rs560660305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220182 | CACCACTGCATTCCA[A/G]CCTGGGTGACAGAGT | 9690 |
rs560661747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235590 | TACTTTGGAATATGT[A/G]TATATTTACAGAAGA | 9690 |
rs560679195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246493 | TTCTGAGTTGACTGT[C/T]TCATGGATGAATGAC | 9690 |
rs560690841 | in-del | -/TTGG | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157235812 | TAAGGGGTTACTAAC[-/TTGG]TTCCAAAACATATCT | 9690 |
rs560726163 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191465 | TGGCTAATTTTTTGT[A/G]ATTTTTGTAGAAACG | 9690 |
rs560729555 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156715 | ATTCCCTTCTTTTTA[-/A]AAAAAAAAAAAAAAA | 9690 |
rs560732481 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157152214 | GGGACAGAGCTGGGA[A/G]GAAGGTAGTCAGGGA | 9690 |
rs560737242 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157242075 | GAAATTGATTGTGGC[A/G]ATGGTCATACAACTT | 9690 |
rs560758000 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157252596 | AGAACCAGCAAACGA[C/G]TCTCCTATAACCATC | 9690 |
rs560771045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157151756 | GAGGGGGCTATGCAA[C/T]TGGACCAAGAGGAGT | 9690 |
rs560794731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253094 | TAAAATACACTCTTT[A/G]TAAATTATGATTACA | 9690 |
rs560795522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263721 | TTTGTGGGAGCGCTG[C/T]TGGCACCGAAAGCAC | 9690 |
rs560811079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157277 | TGAATTCTTAAGCGA[G/T]AAATTTGACTACATT | 9690 |
rs560812095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157169357 | AAATCAAAATAGAAG[A/G]AAGTCATGAGAGATC | 9690 |
rs560812868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140195 | CCATCATTTCTGAAA[C/T]GTTCTTTAAAATGCT | 9690 |
rs560813003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189957 | GGGCACCCATCACCA[C/T]GCCCAGCTAATTTTT | 9690 |
rs560824103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199537 | GTGTAATGGTGTGAT[A/C]TCGGCTCACTGCAAC | 9690 |
rs560826929 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157217314 | AGATCTTATACCTAA[-/T]TTTTGTGATTTTTTT | 9690 |
rs560849872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252403 | AGATAATGAACACAA[C/T]CTTTAATCAGAATGA | 9690 |
rs560850820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157175187 | TCTGTATATATTACA[A/G]TTTTTACTGTAGGTG | 9690 |
rs560854095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219492 | ACCTCTACATCTAAC[A/T]ACAAAATTACAGGAA | 9690 |
rs560859787 | snp | A/G | 0.00080289 | 0.02002 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269271 | GAAGAGAAATTGACA[A/G]TTCACTTATTTGTGG | 9690 |
rs560911475 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157231656 | CCTGGTGACTTTTTA[C/T]AGGAGGGAGCCCCTA | 9690 |
rs560936572 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206685 | CCTCTGCCTCCTGGG[C/T]TCAAGCCATTCTCCT | 9690 |
rs560948100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157237427 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 9690 |
rs560968988 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157235387 | GAGCAATAATTTTAC[C/G]TGCATGAATTAAATC | 9690 |
rs560971315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174422 | GTAATTTAATACTGA[A/T]GTGTTATTTTAAGAT | 9690 |
rs560975611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163158 | TGGGAGGCCGAGGCG[A/G]GTGGATCAGGAGGTC | 9690 |
rs561008395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168429 | TCCTCAATGATAACT[C/T]TACTTCTAGGTTTAT | 9690 |
rs561026737 | in-del | -/TA/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229926 | TTTAATTTATTTATT[-/TA/TT]TTTTTTTTTTTTGAG | 9690 |
rs561031188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251830 | AATTAAAAGTAGTGT[A/C]ACCGTTTAAAAGTTA | 9690 |
rs561060267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265050 | TTTTTTAGTTGTTTA[C/T]AGCTCTTCCTTCGTT | 9690 |
rs561141013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140229 | CCTAGTTTTTCTTGT[C/G]TATCAGTATATTCTG | 9690 |
rs561158052 | snp | A/G | 9.90442e-05 | 0.0070365 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231258 | TCTGTACCCCAACCC[A/G]GCTGCTCAGATGCTT | 9690 |
rs561158743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200806 | CTTTTCATAGAGATG[A/G]GGTCTCACCACATTG | 9690 |
rs561181711 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144957 | ATCTACCCTTACAGC[A/G]TTATACAGAAGAGTG | 9690 |
rs561195222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236949 | GTTGGCCAAGCTGGT[C/T]TCGAAATCCTGACCT | 9690 |
rs561211021 | in-del | -/GT | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157260402 | TGAAGAAATAGATGG[-/GT]CCCCTTCAGAGTTTG | 9690 |
rs561218096 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157198668 | GCCTCCTGAGCAGCT[-/G]GGATTACAGGCATGC | 9690 |
rs561245090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188181 | CATAGGCAAAAGCTG[C/T]CAGTAAGTAAGCAGG | 9690 |
rs561358163 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157165274 | GTTTTTGACCTTTGC[A/G]TCGTTTCCCATATTT | 9690 |
rs561389596 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172744 | CAACGGCAGATAATC[A/G]GGCTTGCTTTCTGGA | 9690 |
rs561394575 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170384 | CATTGCTAATGGCCC[C/T]AACCTTACCCTTTTG | 9690 |
rs561429220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184222 | CTTTGTTAGCACGTT[A/C]ATGGAAGTGTAAATG | 9690 |
rs561435103 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242801 | GTGGCTCAAGCCTGT[A/T]ATCCCAGCACTTTGG | 9690 |
rs561463432 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157158609 | AGCTCATTGTCCATT[G/T]TTAGATAGGGACAAA | 9690 |
rs561481240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157255952 | GGAAAACACCCAGCT[A/G]TGTTAGTACTAGACA | 9690 |
rs561491084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157208737 | TGAAGTTTTGAGTTA[C/T]TGTGGCTGGAATGTT | 9690 |
rs561497715 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217351 | AGACGGAATCTTGCT[A/T]TGTTTGCCCGTGGTG | 9690 |
rs561498995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248094 | TGTTGGCTTCTGTCT[C/G]ACAAGAAGGATCTGT | 9690 |
rs561515420 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192547 | TGTCTGACTACAACA[G/T]TCAAAAGGAGCTTAC | 9690 |
rs561531681 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157165560 | ACGCCACCGCACCCA[C/G]CTAATTTTTTGTATT | 9690 |
rs561554522 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257371 | CTTGGGCTTTTTGCT[A/G]CTGAACTGAAGCAGG | 9690 |
rs561573631 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161357 | TTTAATTAAGTTTAA[A/G]ACAATATTTTTTCTG | 9690 |
rs561599522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247759 | AACCCAAATTTGGAA[C/T]ATAGCCACCCTCACT | 9690 |
rs561622411 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137097 | GCCTGCCACTATGCC[C/T]GGCTAATTTTTTTGG | 9690 |
rs561635503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170125 | ATGCCTGGTTTTTTT[A/T]TTTTTTTTTCTTTTT | 9690 |
rs561644772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157223692 | ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCGAGC | 9690 |
rs561658132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178438 | GTGTTCATTTCTCCA[C/G]TGTCCATTTTTCTTG | 9690 |
rs561677067 | snp | A/G | 0.0001188 | 0.00770623 | intron-variant | UBE3C | GRCh38.p7 | 7:157223117 | GGGTCTGCCTGAGGC[A/G]GGGATGTGTTCATGG | 9690 |
rs561681473 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157261466 | TTTTTATTTTTCTCA[A/G]TGTTCTAACATATGT | 9690 |
rs561756561 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266086 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 9690 |
rs561796887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141997 | CTGCCACAGTTTCCC[C/T]GTGTCGCACGCCCAC | 9690 |
rs561809642 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157166994 | GAGTGCAGTGACATG[A/G]TCTCAGCTCACTGCA | 9690 |
rs561824384 | snp | G/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182187 | CATTTCATCATTCCG[G/T]CGCTTGCAGATGCGC | 9690 |
rs561836967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190571 | TCACGGAAGGTGCTG[A/G]TGGGCGGTGCTGCCC | 9690 |
rs561859170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157161715 | CTCCATGGCCTTCCA[A/G]AGTGCTCGGATTATA | 9690 |
rs561862076 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180550 | TTTCAAAAACTAGCC[C/T]ATGCAGATGGATTGT | 9690 |
rs561865785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148623 | AAGCAGAGGTGTAAT[A/G]GATGTGATAGTATAA | 9690 |
rs561867492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245768 | GCTACTTAAAAAACA[A/G]CATTCTTCAGTCAGG | 9690 |
rs561868415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210478 | CACCTCTGTAGTTAA[C/G]TGTGTTTTAGGCAGT | 9690 |
rs561875227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204892 | TTCTTAAAAGCTCTT[C/T]GCAAGGGTGGGGGAC | 9690 |
rs561901625 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157138997 | AGCGCCGGGTTTGCT[G/T]CCCGCTGGGCGCCCC | 9690 |
rs561906607 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144828 | GTGGATCATCAGTTA[A/C]AATTGATAAACCAAT | 9690 |
rs561923200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211255 | TTTTTTCAGTTCCAA[A/G]AAGCTATTTTTAAAA | 9690 |
rs561955015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167442 | TTGGGTGTTGCTTAA[C/T]TTTTATAGCAGTCTC | 9690 |
rs561956226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249466 | GATTACAATGCGCCA[A/C]CACGCCCAGCTAATT | 9690 |
rs561959740 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141318 | CAAAGGAAGACCATC[C/T]CCAGCATTCCAGAGG | 9690 |
rs561961263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149621 | ATATCCCCTACTTGG[C/G]TTTAACCACTTGAAT | 9690 |
rs561962025 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138541 | TGCCGGCCCCTGCAC[A/C]CCACCCTGCACCCCG | 9690 |
rs561988686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250031 | AAAAATACAAATCCA[A/C]ACACTTCTGGCCCAA | 9690 |
rs561990992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173136 | ACCAACACTTTGTGG[A/G]GCTGAGGTGGGAGGA | 9690 |
rs561995976 | snp | C/G | 3.85631e-05 | 0.00439091 | intron-variant | UBE3C | GRCh38.p7 | 7:157139372 | GGGCGCCCTCGGCTC[C/G]GGGCCTGCGCGGCCG | 9690 |
rs562001596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235092 | GCTACTCCAGAGGCT[A/G]AGGCAGGATAATGGC | 9690 |
rs562007115 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137806 | TCACTTCAGGTGATC[A/C/T]GCCCGCCTTGGCCTC | 9690 |
rs562034665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191275 | TGTGTGTGTAGTGTT[C/T]GTTGGTTTTGTCTTT | 9690 |
rs562054678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217729 | GTAATCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 9690 |
rs562069011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192132 | AATAAAATAGACTTG[C/T]CTTCGTCAGCTTCAG | 9690 |
rs562077059 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207962 | ATGTATTTTTTTGTT[C/T]ACTGACATTGAAAAA | 9690 |
rs562084893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155985 | TGCATAATTTGAAAG[A/G]TAAGGATGTTTTCAA | 9690 |
rs562094314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230460 | CCAGCACTTTGGGAA[A/G]CCAAGGCGGGCAGAT | 9690 |
rs562094648 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185733 | CAGCTTATGTACAAT[G/T]TATTTTAAAATTGTA | 9690 |
rs562098681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157150094 | TATCAAGAGTCTAAC[A/G]AGGCCAGGCATGGTG | 9690 |
rs562105461 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267932 | ATTACGGTGTGGTCA[A/C]TTATTTAGATGGACA | 9690 |
rs562135141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173728 | TAGTTATTTTACATC[C/T]TATTTGTTAACTGAT | 9690 |
rs562135849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235608 | TATTTACAGAAGATC[C/T]AGGGAAGAGAATTTG | 9690 |
rs562137018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167534 | TAAAATGCCTCTCTC[A/T]CTCTCTTTTCTTTTT | 9690 |
rs562155095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218405 | AGTAAGCTGAGATCA[C/T]GCCACTGCACTCCAG | 9690 |
rs562167112 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229171 | CTCCTTCCCCCTATC[-/TT]TTCTGCAAAGCACCT | 9690 |
rs562186177 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176744 | TTCTTGGCTTGGCCT[C/T]ATTTGTATTTTGAGA | 9690 |
rs562257628 | in-del | -/TC | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157265031 | TTTACCAGTTTACTT[-/TC]TGTTTTTTAGTTGTT | 9690 |
rs562261783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157257185 | AATTAAGTACTGGTT[A/G]TGATGTATATATTTT | 9690 |
rs562263363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157256421 | GTGCTGGGATTACAG[A/G]TGTGAGCCACTGTGC | 9690 |
rs562281429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219117 | AGGAGATGACCAGGG[C/T]GGTGCCACTCCAGGT | 9690 |
rs562288747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150818 | TAAAAGAAAGATACT[A/G]GTTGCTTATTGCTGT | 9690 |
rs562296847 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138422 | TCTGTGCGTGTCATA[G/T]ACATAGAACAGGTGG | 9690 |
rs562315079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157173922 | CAGTTTAAGACATGC[A/G]CTAATTTATTATGCA | 9690 |
rs562343774 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268616 | GTCCCGATGCTAGCC[A/G]TGCCGGTCTCCCATC | 9690 |
rs562381878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157263198 | GCTTAGTCTGCCCAC[C/T]GTAGCCGCTATGCTT | 9690 |
rs562396903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167825 | ACAGGCATGAGCCAC[C/T]ATGCCTGGCCTAAAG | 9690 |
rs562409612 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157155177 | TCTGCAAAAAAGAAT[C/T]CCACCCCCTCCACAC | 9690 |
rs562437291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157218203 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAA | 9690 |
rs562450439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143732 | AAGCGGGGAGTGGTC[A/G]TTGACTGAATGCCTG | 9690 |
rs562473617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224074 | AAAGCAGTGCTGTGA[A/T]CATAGCTCACAGCAG | 9690 |
rs562475582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217800 | TGAGACTGTGCCATT[A/G]CACTCCAGCCTGGGT | 9690 |
rs562482485 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157246217 | ACTTATTTAAGGATG[C/T]GCATTTTATAGACTA | 9690 |
rs562504824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205683 | TTAAATTTTGGAAGA[A/G]TGGCATTCATTCATT | 9690 |
rs562541147 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197242 | TAGTCAATGCTGCAT[C/G]AAGAAACTTTAGTGC | 9690 |
rs562627215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192617 | AAGGAAGGAGTCTTA[A/C]CCCACTCCCAAGAAG | 9690 |
rs562642570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240472 | TAGGGCCCACTTGAC[A/G]TTAATATCATAAAGT | 9690 |
rs562680010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156148 | CCTCATTATATTGAG[C/T]TGTTTTTAGAACTTG | 9690 |
rs562715323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213626 | AAAGGAATGTGTTAA[A/G]GTGTTTCGAGATCAC | 9690 |
rs562722043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231023 | CTGTAAGGCTAGTTG[A/C]TGTTATTGCTTGCTT | 9690 |
rs562752003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219515 | TACAGGAAACATAGG[G/T]GTTAGAAGTACATCT | 9690 |
rs562775039 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157229500 | TTTTTTGTATTTAGT[-/AG]AGACGGGGTTTCACC | 9690 |
rs562779489 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157158010 | GAGAGAGAGAGATAC[A/G]TATAAACATGGTGAG | 9690 |
rs562801444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157204977 | TCTCAAGATCTAGAC[A/G]GAGGTTAGGGATTGC | 9690 |
rs562816863 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177575 | TCCCAGCGGCTTGTT[A/T]TGTGTAGCCCCGCTC | 9690 |
rs562889195 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208738 | GAAGTTTTGAGTTAC[G/T]GTGGCTGGAATGTTG | 9690 |
rs562893930 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189612 | TGCCCACTCAGCCCC[G/T]CGGCATTCCTGGCCT | 9690 |
rs562918161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230586 | TGTAGTCTTAGCTAC[G/T]TGGGAGGCTGAGGCA | 9690 |
rs562920458 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157263215 | TAGCCGCTATGCTTC[A/G]TGTCCTAACACCACC | 9690 |
rs562952557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157139505 | CCGGATCTCGGGGCC[A/G]CTCCGGCCGGGACTC | 9690 |
rs563007794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180759 | CTGGATATTTTAAGA[A/G]GTTCTGAAAGTTGTT | 9690 |
rs563010337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150267 | GCCTGTAATCCCAGC[C/T]ACTTGGGAGGCAGAG | 9690 |
rs563042984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187156 | ATTCTACTGTCCAAG[C/T]GTTTCATAAAAAATA | 9690 |
rs563066951 | in-del | -/GTA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244613 | TTATTGATTCTTAAT[-/GTA]GTAAATTACTGAAGT | 9690 |
rs563084580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225277 | AAAAATCAAGATTTG[A/T]TACCTTGACTATTAG | 9690 |
rs563122999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147074 | TATTCACAAAAAAAA[A/C]CTGTGGAATTTTGAT | 9690 |
rs563144196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174577 | CCCATCTCAGCCTCT[C/T]GAATAGCTGGGACTA | 9690 |
rs563150040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222216 | GAGAGTTATAAAGCT[A/G]TTCTGGATATAGTTT | 9690 |
rs563156774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257702 | AGATCGCGCCACTGC[A/G]CTGCACTCCAGCCTG | 9690 |
rs563159619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233058 | TATCCTGCCCTTCCT[C/T]CCCCAGCCCTGGCCA | 9690 |
rs563162816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263542 | GATGATGGGCACATA[C/T]AGTCCCAGCTACTCG | 9690 |
rs563176422 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157265341 | AGAGAACACATAAAT[C/T]ACGTATCTCAAATGT | 9690 |
rs563180056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189572 | TGCATTTGTGACCCT[A/G]CTTACATGTAGATGA | 9690 |
rs563186206 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142961 | AAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 9690 |
rs563222508 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139024 | CCCCTGCAGCGGCCC[A/G]AGCTGTGGCCGGCGT | 9690 |
rs563225467 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | UBE3C | GRCh38.p7 | 7:157144691 | TCCAGTGCTTTTTTT[A/T]AAAAAAAATAGACTT | 9690 |
rs563228996 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141549 | CTGAATACTGTAGGC[A/G]GCTCTTCATGCAATG | 9690 |
rs563289321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221611 | GCTGAGCGTAGTGGC[A/G]GGCACCTGTAATCTC | 9690 |
rs563309729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157244103 | GGGCATGGTATGCGC[A/G]CTTGTAATCCCAGCT | 9690 |
rs563319111 | in-del | -/AC | 0.120326 | 0.21374 | intron-variant | UBE3C | GRCh38.p7 | 7:157264462 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs563319384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265611 | TGCATGGAACACCAT[A/G]TAGCCTCACCATTAA | 9690 |
rs563331444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238573 | ATGCTGACTAAGCTG[A/G]GAAAGGTGCGGGCAG | 9690 |
rs563335429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152719 | TCCGGATGCTGTACG[A/G]CCTCTCCCTCGTGTC | 9690 |
rs563335457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159216 | GCATACACACCATGA[C/T]TGTGGAGGAAAGAAT | 9690 |
rs563424597 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260458 | GGAGAATCTCTCGAG[C/T]GCAGGGAAAGCTGGG | 9690 |
rs563441811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183131 | CCCACACACCAAGCA[A/G]TTCTTCAGTGGACAC | 9690 |
rs563473607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243640 | GACACTGGGACAACA[C/T]GGATTTTTTAGTGCC | 9690 |
rs563476717 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152022 | TTTTGTGTGCTGGAC[C/T]GGGTAGGATTCTTAG | 9690 |
rs563514217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141791 | TTGTCGTTTGTGCCC[A/G]GCTGCTTTGGCTTGG | 9690 |
rs563527512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149427 | TGAGACTAATTGTCT[C/T]ATTGTCTCATTTTCT | 9690 |
rs563559063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259854 | ATAGTAAGTCAAGTA[C/T]ACCTCAATTAAGCTG | 9690 |
rs563564575 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157155151 | TCATAGAGATTCTTA[A/T]TTCATGTAGGTCTGC | 9690 |
rs563564607 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157148733 | GATCAAATTAGTTCT[G/T]TTTTTTTTTTTTTTT | 9690 |
rs563565713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183539 | GTGCGTGGGGCTGAA[A/G]GTTCCAACCCTCTGA | 9690 |
rs563568029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160222 | TGAGACTACAGGTGC[A/G]CGCCACCACGCCCAG | 9690 |
rs563606188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190055 | ATCTCCCGCCTCAGC[C/T]TTCCAAAGTGCTGGG | 9690 |
rs563621711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147857 | AGTCATTTTAGAATA[C/T]TGAGCCCGTCTTGCG | 9690 |
rs563680979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239947 | GAGCAAGGATGGGAA[A/G]AGCAGTGTTCCCAGA | 9690 |
rs563699740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160634 | TAGTTGGTGTCTGCA[A/G]AATTTCTCCCCTTTA | 9690 |
rs563718929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142632 | AGTCACTTTGGGGAG[C/G]TAAACATTGATTACA | 9690 |
rs563749484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228859 | TAGACTATTTACACT[A/C]CAGGTACGGTAACTT | 9690 |
rs563770427 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157202668 | TCAAAAAAAAAGAAA[A/G]AAAGAAGTCTATGCC | 9690 |
rs563771911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184272 | TTGGTTTTTTAGGCA[A/G]AATAGGATCATACTA | 9690 |
rs563828115 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226680 | TGTTGGAACAGTGGA[A/G]GAAAGCTGACATCAG | 9690 |
rs563829326 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157213224 | AACTTAAAATCCACT[-/A]AAATTTGTATATTCA | 9690 |
rs563835064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249253 | GGCTCCCCCACCTCC[C/T]GCAGGCAGCCACCAG | 9690 |
rs563888032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229503 | TTTGTATTTAGTAGA[C/G]ACGGGGTTTCACCAT | 9690 |
rs563903309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210258 | AAGTTGTTGTAAGAC[C/T]TTTTGAGTTTAGAAT | 9690 |
rs563907339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222569 | GGACTATAGGCGCGT[G/T]CCACCATGCCCAGCT | 9690 |
rs563917292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191209 | GATTTAGATAAACAG[C/T]GGTGCGCCTCGAAGC | 9690 |
rs563942109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227987 | GGTGTTTTGCTACGC[A/G]AATTAGTAAAGTCAG | 9690 |
rs563944499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217299 | GTATTTAAAAGAGAT[A/C]GATCTTATACCTAAT | 9690 |
rs563955848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197649 | ATATCTGCTTCTAGC[A/G]GTGTCAGGCTTTCAT | 9690 |
rs563956823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157267392 | GCGCCATTGCCCTCC[A/G]GCCTGGGCGACAGAG | 9690 |
rs563962763 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157183707 | TAGGTGCTTTCTGAC[A/G]TGAACGGGGACAAAA | 9690 |
rs563972520 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260455 | ATAGGAGAATCTCTC[A/G/T]AGCGCAGGGAAAGCT | 9690 |
rs564041011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184137 | AGTCAGACCCTCAAG[C/T]AGCCTTTGCAGAGAA | 9690 |
rs564046382 | in-del | -/T | 0.496778 | 0.0400063 | intron-variant | UBE3C | GRCh38.p7 | 7:157158051 | TACACTCTTTTTTCC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs564087828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228626 | AGCCAAATGGCTTAG[A/T]TGTGTTTACCTGATT | 9690 |
rs564095035 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180083 | GAAATGTGTCCCAAT[A/T]TACGAAATGCTTAAA | 9690 |
rs564095099 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154210 | GCTGTAATCCCAGCA[A/C]CTTGGGAGACTGAGG | 9690 |
rs564127590 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178052 | AAAAGGATTGGGGTG[A/G]GGGGAAAGAGGGAGG | 9690 |
rs564209027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147231 | TATAATTTTCCTTAT[A/G]TATACCTTATACCTA | 9690 |
rs564229269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241519 | TAGCCACAGGCTGCC[A/G]CGCACACCCGCGAGT | 9690 |
rs564235594 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157249318 | CTTCACATCGATAGA[G/T]TCTTTTTTTTTTTTG | 9690 |
rs564247932 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150920 | CTGCGCTGGCCTGTT[C/G]ACAAGCCTGGAAGTT | 9690 |
rs564290626 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262441 | TTTTTTTTTTTGAGA[G/T]AGAGTTTCGCTCCTG | 9690 |
rs564295234 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260214 | CATTCAGAATCGTAA[A/G]ATAGAAAACATAGAA | 9690 |
rs564312427 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212885 | ACCTCGGCCTCCTGA[A/G]TAGCTGGGACTACAG | 9690 |
rs564337557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157172120 | TCACCGCAACCTCGC[C/T]TCCTGGGTTCAAGCG | 9690 |
rs564358210 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157255201 | GATAGATAAATGGCC[A/T]GTAAGCAAATAAGCA | 9690 |
rs564358516 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264967 | ATCATTTTTCCTCAT[A/G]TTATTCTTTGAGATA | 9690 |
rs564380887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160796 | TTCTGTTTTCTGCTT[C/T]TCTCTTTCCTTCTAC | 9690 |
rs564392362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235508 | GATAAACTCATTTCT[C/T]CTCTGTTTATTGACA | 9690 |
rs564401184 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157153261 | AGCTGTGTGAGCAGA[C/T]GCTAGATTGTTGGCA | 9690 |
rs564446507 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157223039 | ATTAGGACATCTTTA[A/G]TATTCGATCAAGTTA | 9690 |
rs564490942 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157161422 | ATTTTCTTTGATAGA[A/G]AGTATCTGGAGGATT | 9690 |
rs564511256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241990 | GGGTGAGTGATCGCC[A/G]GGGCTGGGAGGAACC | 9690 |
rs564523053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167331 | TTAGTCTCAGCTTTG[C/T]AGATGGCATTCATAG | 9690 |
rs564527481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150005 | GGTGGTCAAATTACA[C/G]GCTGTAATACCTGCT | 9690 |
rs564537308 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148223 | CTCCTGTCTCAGCCT[C/G]CCAAGTAGCTGGGCT | 9690 |
rs564537317 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183069 | TTTTTCTTACTCTCT[C/T]ACTCAACACTGAAAA | 9690 |
rs564538553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223787 | TAGTTGGGCGTGGTG[A/G]CATGTACCTGTAGTC | 9690 |
rs564595011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204180 | GTAAATGTCTCATAT[G/T]TCCTACTGGGAATAA | 9690 |
rs564673694 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205338 | TAATTACCCTGTCCC[-/T]TTTTTTTTTGGACCC | 9690 |
rs564674369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214317 | ATAATTTGATAATGT[G/T]TGTAATCTGTAGAAA | 9690 |
rs564682249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224105 | CCTCAAACTCCTGGG[C/T]GCAAGCCACCATCTC | 9690 |
rs564687831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200882 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 9690 |
rs564701201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146242 | ATATTTTTATGGATC[C/T]ATTTCTTTTTTTTTT | 9690 |
rs564707701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185702 | CCTTTAGGTTTCTGT[A/G]TAATCTGTTCACTTA | 9690 |
rs564712243 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214594 | ACTATTAAATCTGGA[C/T]TTATTTAAAGTATCA | 9690 |
rs564756811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191787 | TTTTTCATTGTATGT[A/G]TAGAATTAAATATAT | 9690 |
rs564783131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191246 | CTTCTTTTCTGTGCA[C/T]GCGCGTGTGTATGTG | 9690 |
rs564800442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170782 | CTAGGTCAGTGGGAC[A/G]TGCACCCTGAATACC | 9690 |
rs564840329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149490 | AGTAAAGCACCATAC[A/G]GTATTTAAGGAGGCA | 9690 |
rs564863691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157247362 | GTACCTAGTAAGTGC[C/T]CAAGGAATGGTAACT | 9690 |
rs564871309 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213506 | CTTTGAGCACATTTA[A/G]TCACTTTATGTGATT | 9690 |
rs564874085 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157152224 | TGGGAGGAAGGTAGT[C/T]AGGGAGAGAGCTGGG | 9690 |
rs564883947 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157216265 | AACTCAGAAATACTC[-/TT]TCAGGAAAAAGTTGT | 9690 |
rs564890511 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258194 | CCAAGAAATCCTCTC[A/T]CTTCAGCCTCCCAAG | 9690 |
rs564898476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254515 | CAATTCTCCTGCCTC[A/G]GCCTCCCGAATAGCT | 9690 |
rs564909895 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238035 | CCAGCCTGGGTGACA[A/G]AGACCCTGTCTCAAA | 9690 |
rs564945827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157163985 | TGACAGAATGTGTGT[G/T]TATGTGTGTTTAGCT | 9690 |
rs564948231 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253292 | CCCAGGTCTGTGTTT[A/C]CGCTGTGTTGCTTTT | 9690 |
rs564955372 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256000 | TAGATCTGTGGCCAC[A/G]TGCAAGCCCCTTCTC | 9690 |
rs564964367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170765 | AGCAGTTGCCAGCAC[A/G]CCTAGGTCAGTGGGA | 9690 |
rs564991783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157200252 | ACTGTTTTTTCAGTG[A/G]TGTACCCTTATTGCC | 9690 |
rs565026064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157206355 | GCAACCTCCGCTGCT[C/T]GGGTTCAAGTGATTC | 9690 |
rs565026253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259421 | TTGGGAGTGTACAGA[C/T]GGCAACATATTTTCA | 9690 |
rs565063787 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195179 | ATCCTCCCAGCTATT[G/T]CAGAAAAAGCCAAAA | 9690 |
rs565098947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195671 | AGGAGAATTATGCCC[C/T]AGAAATCACACCCAG | 9690 |
rs565115410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188884 | CCCTCACTGATTAAT[A/G]TTAGTCCCTTTTATT | 9690 |
rs565127590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157181957 | TTAAGTTTACTTTAG[A/G]TTGATCTAGTTGATA | 9690 |
rs565188919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165752 | TTGTTATTTCAGTTC[C/T]AGAATTTTCTTTCAT | 9690 |
rs565192077 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157264617 | ACAGAGTTTCACTCT[C/T]ATTGCCCAGGCTGGA | 9690 |
rs565198521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176335 | GCTGGAATGCAGTGG[C/T]GTGATCTCGGCTCAC | 9690 |
rs565236708 | in-del | -/ATTAAA | 0.344815 | 0.231323 | intron-variant | UBE3C | GRCh38.p7 | 7:157180580 | TTTTAATGTGCTACC[-/ATTAAA]AAATACGCTTGTATA | 9690 |
rs565236869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182617 | GGCCTGTTTCCCTCC[C/G]TCTGCTAAATTTCCA | 9690 |
rs565244446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247816 | TTGTGCTGCAGGGCA[A/G]AGTGGCATATGCGGT | 9690 |
rs565248498 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157208098 | TTTTTTTTTTGATAC[A/G]TGGACTTGATGTGTC | 9690 |
rs565281657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215186 | TATCTGCATGACCAA[A/G]TTGCTCGAATAACAC | 9690 |
rs565286007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140866 | CCCTTTAAAAACAAA[A/C]CTCTTTTTATTGAGG | 9690 |
rs565313074 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143404 | TCTGACAGAATAGAA[A/G]GGTCAGAAACACCCA | 9690 |
rs565360065 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225810 | AGTGAGCTTATCTGG[A/G/T]TGTGTTAGCGTGCCC | 9690 |
rs565360382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231884 | GTGACTATTAGTTTA[A/C]TAGGACTGCCGCAAC | 9690 |
rs565375116 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150628 | CAGCCATTTAAAATG[C/G]TCATGATGCGTATTA | 9690 |
rs565399015 | snp | A/C | 3.36016e-05 | 0.00409874 | intron-variant | UBE3C | GRCh38.p7 | 7:157231376 | ACCAAAAGATGTTGA[A/C]ATTTTATGTTTATGT | 9690 |
rs565403823 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168403 | GCCATTTTGGAAAAC[A/T]GTGTGGCAATTCCTC | 9690 |
rs565418629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220913 | CTACCATGTAGAAAA[A/G]TTTCATCACCCACAA | 9690 |
rs565438686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202268 | GACTTAACATATTTT[A/C]ACTGAGTATGTAATA | 9690 |
rs565439641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202579 | GGAGAATCGCTTAAA[A/C]CTGGAAGGCGGAGGT | 9690 |
rs565453923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157159990 | GATTATAAACAGTTT[A/C]TTTTACCTTGAGGAA | 9690 |
rs565489858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157247617 | GAATCGCTTGAACCT[A/G]GGAGGCGGAGGTTGC | 9690 |
rs565559034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157144893 | TACATTCAGGTTCAC[A/G]CTGTGTGTTGTGCAT | 9690 |
rs565595260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157151976 | GTACCATGTGTGTAT[C/T]CTATTTCCAGAACCC | 9690 |
rs565652267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145641 | GAATGTCATATAGTT[A/G]GAATCATATACTATG | 9690 |
rs565655493 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157253376 | CTGTGAGTATAGCCA[C/T]GTACTAATAAAAAGT | 9690 |
rs565667544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157193740 | TACATGCATCATGCA[A/G]AATGACTGACCTCAC | 9690 |
rs565678240 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145674 | ATCTTTTCAGATTGG[C/T]TTCTTTCACTTAGTA | 9690 |
rs565727755 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219006 | TACCTCAGGCAAAAC[-/AG]ATAGTGTGTGATCTT | 9690 |
rs565734297 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191891 | AAGTAAATTTTGTCT[A/G]TAATTTCATAGCTGC | 9690 |
rs565744319 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269492 | GATGGCCTACACTCA[C/T]TGAGAATCAGAGGTC | 9690 |
rs565767275 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157221962 | GCAGCCTTGACTTCC[G/T]GGGCTTCAGCGATCT | 9690 |
rs565769718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264170 | AGGTGTGAGCCAACA[C/T]GTTCGGCCTGTTAAG | 9690 |
rs565779914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170202 | GTGTTTTCGTTGTCA[A/G]TTTCCACCATTCCTG | 9690 |
rs565800477 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206373 | GTTCAAGTGATTCCC[C/T]TGCCTCAGCCTCCCA | 9690 |
rs565805458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158342 | TGAAACCATGCACTC[A/G]TACTTTATTTTGAAA | 9690 |
rs565818637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175986 | AAAAATAAAGGAATC[A/G]TGCTTCACTCAACAG | 9690 |
rs565845793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157215262 | TAGTGGCCTGAGATA[C/T]CAACCCAAGTACCCT | 9690 |
rs565859467 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157189611 | GTGCCCACTCAGCCC[C/T]GCGGCATTCCTGGCC | 9690 |
rs565998052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265431 | GGCCATCAGAGGACC[A/G]ACACGCCCATAGGTC | 9690 |
rs566027038 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157182834 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 9690 |
rs566064084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238631 | TATGGAGGCTTAGTG[A/C]GGGGCAGTTGAGGAT | 9690 |
rs566071418 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170195 | GATAATGGTGTTTTC[A/G]TTGTCAATTTCCACC | 9690 |
rs566076981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157232722 | CTGTAAGAATCAGAG[C/T]TATAATCATTTTCAA | 9690 |
rs566085125 | snp | A/G | 0.000972514 | 0.0220298 | intron-variant | UBE3C | GRCh38.p7 | 7:157201852 | CTCAAGGGCACAGGA[A/G]GTGGCAGCCTAATCA | 9690 |
rs566124668 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229888 | AAAGTGCTGGGATTA[C/T]AGAAGTGAGCCTCTG | 9690 |
rs566163689 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227424 | ACTCCCTGGGCGTGG[C/T]GCAGTGGCTCACGCC | 9690 |
rs566165277 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157161940 | CCAGGTGTGATGGTA[G/T]GCACCCGTAGTCCCA | 9690 |
rs566180484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260034 | GAAGTAATGAATAAT[A/T]AAGACGTATAAACTT | 9690 |
rs566200711 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157146707 | TTGCCCAGGCTGGAG[G/T]GCAGTGTTGTGACCT | 9690 |
rs566218697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250208 | CTTTAGCATATGGGG[C/T]TTTGTTGTTGTTGTT | 9690 |
rs566220160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157208318 | TGGCCTCATGGATTC[C/T]TCCTGCTTCTGCCTC | 9690 |
rs566244488 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175489 | CCGTGACTTTCTTGC[A/G]TTCAGTGTCCGAAAG | 9690 |
rs566262301 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244434 | TTTGTTTTTTAAATT[A/G]TATGGTTAATATGAT | 9690 |
rs566319577 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157264131 | TCAGCCTGTTACGTG[-/CA]CACACACACACACCT | 9690 |
rs566322288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153480 | AATTTGTTTTTAACA[C/G]AGTCCAGGTCTCACG | 9690 |
rs566332351 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177289 | CATACTGGTCACTCA[C/G]ATGGCTCTTTTTCAA | 9690 |
rs566352201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157153919 | GACGGCTTGGTGGGG[C/T]GGGGGCGAGGTTGCA | 9690 |
rs566358939 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189737 | GGGCTTCTCAGTTTC[C/G/T]TTTGTGGGTTCTTTT | 9690 |
rs566407361 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160982 | CATGAGAGTATTGGA[A/G]AAACCCAAATTGAGG | 9690 |
rs566430443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157198075 | TCTCCTCTTTTAACA[A/G]ACTCCAGAAATTGAG | 9690 |
rs566435216 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268288 | TAGGTTTGGAAAAGA[A/G]ATGATGATGGTAATA | 9690 |
rs566455463 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204654 | ATTTTCAGTACTTGC[-/T]TATTGAAATCAGCCA | 9690 |
rs566457835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191457 | ACCACACCTGGCTAA[C/T]TTTTTGTAATTTTTG | 9690 |
rs566459087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155685 | CATTTTCCCCCCATT[C/T]GAAATCATCTTGGTA | 9690 |
rs566474623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235171 | CTCCAGCCTGGCAAC[A/C]AGAGCAAAACTCTGT | 9690 |
rs566493587 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138517 | TGGCCGCTCCCAGCC[A/C]GCTCCGGGTGCCGGC | 9690 |
rs566567593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150428 | TCTAATCCAGCAGAA[C/T]AAATTTCTACATTTA | 9690 |
rs566586790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245089 | CATTTAGCTGATGCA[A/G]TCATAGTTTTTAGTG | 9690 |
rs566589683 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157266413 | AAATTTGAATTTTTC[-/T]TTTTTTTGGCAATAA | 9690 |
rs566615012 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157211433 | TGACTACTAAAGTGG[A/G]TGCTATATGCAGTAA | 9690 |
rs566616734 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186278 | AAAATACAAAAATTA[C/G]CTGGGTGTGGAGGCG | 9690 |
rs566650710 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163556 | CAGTTTTACCTGTAC[A/T]CATTTGTATATGTGA | 9690 |
rs566653463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157240505 | AGTGAGACCAGCCGT[A/G]TGGGTTACTTTTTCT | 9690 |
rs566659507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157206161 | TGCAGGTGAGCCTAT[C/T]AGCTAAAAGTTCCAT | 9690 |
rs566679672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198628 | CAACCTCCACCTCCA[A/G]GGTTCAAGCGATTCT | 9690 |
rs566691004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143398 | GGCGTGTCTGACAGA[A/C]TAGAAAGGTCAGAAA | 9690 |
rs566696980 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214275 | TAATTTAGTAGAAGA[A/C]TGTAAATGAGAACTT | 9690 |
rs566702478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262712 | AGGCATGAGCCACCG[C/T]GCCCATCCTCTTCAT | 9690 |
rs566717163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149734 | CATAGAATAGCCTCA[A/G]AAGAAGTTCTTGCAA | 9690 |
rs566734197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229731 | CTCCTGGGCTCAAGT[A/G]ATCCTCTTGAGTAGC | 9690 |
rs566761895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184271 | TTTGGTTTTTTAGGC[A/C]AAATAGGATCATACT | 9690 |
rs566803810 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216791 | CTGTGTGCTCCTCCT[C/T]GAGTGAATGTATGGC | 9690 |
rs566822334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157251944 | GTTCAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 9690 |
rs566835978 | in-del | -/CAG | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157152928 | TGCCAGGTGTGGTGA[-/CAG]TGCACGCCTGTAATC | 9690 |
rs566864634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157205941 | TTACGGCCCCGCTAA[G/T]TAGAACAAGTGGCCT | 9690 |
rs566867327 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157248740 | ATAGCTCCAAAGCAC[C/G]TTAGCCCTGGCGTCT | 9690 |
rs566915615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241558 | AATCAAACCAGGAAC[C/T]GCAGGGTTGGTGAGG | 9690 |
rs566917670 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157200392 | TGGAACAATGCATTT[C/G]ATGTTTTGGATTGAG | 9690 |
rs566919889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168096 | GTGGCTCATGCCTGT[A/G]ATCTCAGCATTTTGG | 9690 |
rs566923085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157156672 | TGTCAGAGCTGTTCT[C/T]TACATACATAATCAT | 9690 |
rs566932948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257299 | GCCTGTGAACAAACC[A/G]TACATTTGGAGGGAC | 9690 |
rs566943161 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213474 | AGAGCCACAGGCCTA[A/G]CCCTGCAGATAACTC | 9690 |
rs566951284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237044 | GCAAGACAGTTTTCT[A/G]TGTAAGTTTATTTCT | 9690 |
rs566958029 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268366 | TTGTTTTCAGTATAC[C/T]GTGGCCTGCCTCATG | 9690 |
rs566960316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156330 | TTTTTTTTTTGAGAC[A/G]GAGTCCTGCTCTGTC | 9690 |
rs566983249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157251358 | CCATGAAATTTTAGA[C/T]GACTAATTTACATAG | 9690 |
rs566994544 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157155779 | TTCAGAGAAGATAAC[A/C/G/T]ATAGTACCTAAAGCT | 9690 |
rs567003261 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138653 | GCCCCTCGCCGCGCT[C/T]CCCCAGCACGCACCA | 9690 |
rs567011540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157140152 | ACACTGTGTGGTCTT[A/G]TTCCCGCCCCTCCCT | 9690 |
rs567014038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245968 | TGCACACTCCAGCCC[A/G]GGCAACAGAGGGAGA | 9690 |
rs567017768 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166352 | TTTTTAAAAATACTT[-/A]ACTCTTTGGTAAGTT | 9690 |
rs567032444 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157195797 | ATAATGGGTTGTGAC[-/T]TTTGAGCACCTATGA | 9690 |
rs567048202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157151174 | CTGTGGACATAATCC[C/T]GAAGCCACCGTAGAA | 9690 |
rs567063305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168587 | AACGTGGTCCATCCA[A/T]ACAATGGAACATTAC | 9690 |
rs567103126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164061 | AAGGGCAGTTTCCAG[A/T]CTGGAGAAGGAACAT | 9690 |
rs567139739 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145804 | ACAGAATAATTGATG[G/T]GAAACTATAATAGAG | 9690 |
rs567166843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180320 | TATGTTAGTCACTTT[C/T]TTAAAAAAGTCTCTG | 9690 |
rs567180422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241144 | AAGAGACCACAGCTA[C/T]TCACGCAGAGTGCTC | 9690 |
rs567183058 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182948 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGATG | 9690 |
rs567183232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157151098 | GGTGTATTTGTCCAG[A/C]CCACTCTCGGGGTGA | 9690 |
rs567186629 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251618 | GGGGCTTTATGGATT[C/T]CAAGTGAAAATAGAC | 9690 |
rs567195854 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268783 | AGGGAAGAGGAGTGT[C/T]GGTAGTTCTTGCAGT | 9690 |
rs567211066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192340 | GCTTCCTTTTCGATC[C/T]GCCATCTGCGGTGGA | 9690 |
rs567223783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157162613 | AGCTCAATCCTGGCT[C/T]ACTGCAGCCTTGACC | 9690 |
rs567232602 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157263280 | GGCACCTGTCGTAAC[A/G]CCACCTTCCCCGGGC | 9690 |
rs567243530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186367 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTC | 9690 |
rs567249777 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167270 | TCAAGCCCAGGAACT[A/G]CATCTACATGACCTG | 9690 |
rs567258396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168001 | GAAACAAGAAAGTGA[C/T]CTTTAAAATAGATGC | 9690 |
rs567363339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198733 | AGAGACGGGGTTTCA[C/T]CATGTTGACCAGGCT | 9690 |
rs567372346 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157144484 | CAGGAGTGGCATAAC[C/T]TTCAGAGTCTTCGAG | 9690 |
rs567378260 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225845 | TGTCCCTGCTCTGCA[A/G]AAGGCTGAGGCGGGA | 9690 |
rs567402341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198151 | TGAAACCATTGCTCC[A/T]CAGTTTAAGCAAAAT | 9690 |
rs567404775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175306 | GTGAATGATGGCCAT[C/G]CTGGTTACTGGAGAA | 9690 |
rs567407074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230826 | TTGCTGTAGATTCTG[A/G]AGGACCAATTCCCTG | 9690 |
rs567425307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174754 | TGGCTGGAAAATGCA[C/T]ATACCTCTAAATAAA | 9690 |
rs567447228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142102 | TGTAGTTTCTTTGTG[A/G]TTTTAATTTTGTTTC | 9690 |
rs567471904 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138691 | CCCACTCCGCCGCGT[A/G]CCCAGCCCGCGTCAC | 9690 |
rs567512124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144048 | CTGCGGAGCTGGGAA[A/G]AATTGGGTGATTTGA | 9690 |
rs567600193 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157169493 | CAATTCTACTGCCTC[A/G]GCCTCCCGAGTAGCT | 9690 |
rs567615316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157201032 | TTACAAATTTTAAAC[A/G]TGTTAAGTAGGCCAG | 9690 |
rs567618980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157247027 | TCCCAAGTAGCTGGG[A/G]TTATAGGCATATGCC | 9690 |
rs567638264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157258605 | GCTGTGATTACAGGC[A/G]TGCGCCTCCATGCCC | 9690 |
rs567670949 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157252667 | TGAAACAATCTTTCT[A/G]TAAATGGTAAGAGAC | 9690 |
rs567679903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157163513 | CTCTGACATTGGTAC[A/G]GAGCACCAGTCTTAC | 9690 |
rs567740224 | in-del | -/AGT | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157183266 | CAGAGGCCGATTACA[-/AGT]AGTAGGTTGTCACCT | 9690 |
rs567741176 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210437 | TTAAGAAAATACTAT[C/G]TCTATTATGAAGTTG | 9690 |
rs567752988 | snp | C/G | 0.031825 | 0.122064 | intron-variant | UBE3C | GRCh38.p7 | 7:157231919 | TACCACACTCTTTGG[C/G]GGGGGAGGGAGGCTT | 9690 |
rs567773224 | in-del | -/AAAAG | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157249033 | CTTTTTAAAAAAGAA[-/AAAAG]AAAGGTCTATATTAG | 9690 |
rs567775096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157139698 | AGGAGGCCGGTGAAC[C/T]CTGGCACGCTTTGTG | 9690 |
rs567797612 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157213188 | AACACATCAGATGGA[C/G]ATAATGCTATTGTAT | 9690 |
rs567801504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187751 | CCGGCTAATTTTTTG[C/T]ATTTTTAGTAAAGAC | 9690 |
rs567802751 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142987 | ATTCTCCTGCCTCAG[C/T]TTCCCGGGTAGCTGG | 9690 |
rs567846733 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269583 | GTGCTCCTATCCGAC[C/T]AGCCACGGGTGTTGG | 9690 |
rs567850086 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213420 | CTGTGGTGGGCTTGT[C/T]TTAGTGCTCCAGGTG | 9690 |
rs567874646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157164129 | GAAGATCTAGAAAGC[C/T]GTATTATAAATATAA | 9690 |
rs567881284 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157231467 | TGCAAAAGCACTGCA[C/T]GAAACAAATTTGTAT | 9690 |
rs567896017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152051 | AGGACTATTTACATA[C/T]TAACATTACTGTCAC | 9690 |
rs567918090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237135 | CCTGAATTCAGTTGA[C/T]TGCTGCACCTAAATA | 9690 |
rs567922040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164716 | TGACAAATATTTATT[C/G]AGAACTTACTATGTA | 9690 |
rs567932699 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190895 | GCTTTTTTATGCCTC[C/G]ATGGTGTTTCGTGCC | 9690 |
rs567932736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157579 | GCCTTTGACCTACAA[A/G]GAAATTTAACCTGCA | 9690 |
rs567934454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214667 | TTCATACAAAAAGAT[C/T]GTACTTCTGTTCCTT | 9690 |
rs567989746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242232 | CAGCAGTCAGTATCA[A/G]TCGGAGTTCATGGAT | 9690 |
rs568016103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157248894 | GGGGTGGCCGTTCAG[C/T]AGCTTCCCGGCAGGA | 9690 |
rs568038143 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259152 | TGAGCACATGTTAAA[A/G]ATGAACATTTTCAGG | 9690 |
rs568045150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202794 | AGTAGTGATAATAGC[A/G]GTCACTGTTACTGAC | 9690 |
rs568057878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216844 | GCTCACGTGTGTGAC[A/G]CGGATATGTTCTTTC | 9690 |
rs568080878 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157136977 | CTGTTCCCCAGGCTG[C/G]AGTGCAGTGGCGCGA | 9690 |
rs568092545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172163 | GAGCGCCCTGAGTAA[C/T]TGGGGTTACAAGCTT | 9690 |
rs568118070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190362 | CAGGCCCGTCATCTA[C/G]TTGGTTGTCTGTACC | 9690 |
rs568140410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157223459 | GTGCCTGGCTGATTA[C/T]ATAACATACTTTTCT | 9690 |
rs568160189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148262 | CCCACCACCAGGCCT[A/G]GCTAATTTTTTTGTA | 9690 |
rs568165438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157255405 | AAAAATCATTTTTAC[A/G]TATAACCTGTGTGTA | 9690 |
rs568176761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157229016 | TTGAGATGCTCCAGG[A/G]CAGATATGTTTGGGT | 9690 |
rs568180250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248676 | CAGCGTTTGACTTCC[A/G]CACATTTTAGTTAGA | 9690 |
rs568194297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222622 | GTAGAGGCAAGGTCT[C/T]TCTGTGATGCTCAGT | 9690 |
rs568195917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233966 | TGACCATCTTTTCAT[G/T]TGCTTCATGACTTCT | 9690 |
rs568212124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239725 | ATGTGTATTTGCTGC[G/T]GGAAATAAGTCAGTG | 9690 |
rs568266025 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227657 | GTGAGCCGAGATCGC[A/C]CCACTGCACTCCAGC | 9690 |
rs568288295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157225167 | GCCAATGTGCCTGGC[C/T]GGATTTTTAAAATTT | 9690 |
rs568293597 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157239404 | AAAGCTCCTTGCAGT[G/T]TTTGGAAGGCAGGAT | 9690 |
rs568319895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185250 | TGAAAGCAGAACATG[C/T]GGACCCGTGAACCGG | 9690 |
rs568350561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217540 | TAGTATGATACGTTA[A/G]TAAAAAATTTAAGTG | 9690 |
rs568354651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157143198 | GTCACACTGATTTCT[A/G]TCTTTAAATATTTCT | 9690 |
rs568374519 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174231 | GCTGGGCGTGGTGGC[A/G]GGCACCCGTAATCCG | 9690 |
rs568393018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244213 | CGCTCCAGCCTGGGC[G/T]ATAGAGTGAAACTCC | 9690 |
rs568421720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157178254 | GACCAGAAATATATC[A/G]TTGTTCTATTTGGGG | 9690 |
rs568507336 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157261884 | GAATTAATGCAAATT[C/T]CCGTTGTACTGTATT | 9690 |
rs568509093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156922 | CAGTGAGTTATTAAT[A/G]TGGTCCTTATTATAT | 9690 |
rs568531327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267127 | TCAATGTAATTTTTT[A/T]AAAAAGCAAATGTGG | 9690 |
rs568560882 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246730 | ATTCCAGTGCTGCAC[C/T]TCCAGACAGTAGGAA | 9690 |
rs568562371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184582 | ATGACTTTTTTTGGT[C/G]TTAAGCAATTGAAAT | 9690 |
rs568572178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190857 | GCAAAAAGGCATATC[G/T]TGCATTTTCTTGATC | 9690 |
rs568572551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267347 | GAATCGCTTGAACCT[A/G]GGAGGCAGAGGTTGC | 9690 |
rs568617512 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157178056 | GGATTGGGGTGGGGG[G/T]AAAGAGGGAGGAGTG | 9690 |
rs568640695 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262670 | CGGTGATCCACCCAC[C/T]TCAGCCTCCCAAAGT | 9690 |
rs568671436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191408 | TGATCCTCCTACCTC[A/G]GCACCCTTGAGTAGC | 9690 |
rs568680662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172878 | GCACCTATTGCCTTT[G/T]AGTGAGGTCCTCAAT | 9690 |
rs568716375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256583 | TCCTTCATATCTGTG[A/G]GTTCTGTCCACATCC | 9690 |
rs568785122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217948 | GAATCCCTTGTGCCC[C/T]GGAGGCGGAGGTTGC | 9690 |
rs568790753 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178800 | TACAAGATGCTAGCT[A/G]TGTGGTGTCAGTGAT | 9690 |
rs568807771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157203523 | GAAATTATCGTTTAC[C/T]CATAAGTGCCTCAGC | 9690 |
rs568822642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166652 | GCCTGAGGCAGGAGA[A/G]TTGCTTGAACTCGGG | 9690 |
rs568829953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157244237 | AAACTCCGTCTCGAA[A/T]AAAAAGAAAGAAAGA | 9690 |
rs568841220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157248938 | CCTCACTCCTTGCCC[A/G]CTCAGAGCCACCTCA | 9690 |
rs568844844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210577 | ACAGATGAGGTCATG[C/T]ATATGATGGTAGAAC | 9690 |
rs568850112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157197420 | CTTATCTTAAGGTCT[A/G]TTCCTAATCCAGATT | 9690 |
rs568860973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157167090 | GTGCACCACCATGCC[C/T]AGCTAATTTTTTGTA | 9690 |
rs568890516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157218483 | CCATGTCACAGAAAT[A/G]TTCGAGGAGAGAAAA | 9690 |
rs568906526 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157210009 | GATGGTGAAACCCCA[G/T]CTCTACTAAAGATAC | 9690 |
rs568953785 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157249596 | GGGATTACAGGCGTG[A/C]GCCACCGTGGCCGGC | 9690 |
rs568959764 | in-del | -/AAC | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157153840 | ACAAACAAACAAACA[-/AAC]AAAAAACGGGCATGG | 9690 |
rs568963725 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223900 | ACTCCAGCCTGGGCA[A/G/T]CAAAGCCAGAACCTA | 9690 |
rs569009586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157161809 | AAGCATGGTGTCTCA[C/T]GTCTGTAATCCCAGC | 9690 |
rs569024717 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217541 | AGTATGATACGTTAG[C/T]AAAAAATTTAAGTGG | 9690 |
rs569062994 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157184872 | AAAATAAGAGAAGAC[-/AAAG]AAAGGAACAGAAGAT | 9690 |
rs569118506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213049 | AGGTGTGAGCCACCA[C/T]GCCCGGCAGTGTGTG | 9690 |
rs569141817 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157235850 | TCTGATTACAGAGTT[-/A]AAACTTTGTGCTAAT | 9690 |
rs569175282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224415 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9690 |
rs569193771 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157166558 | CCAGCCTGACCAACA[-/T]GAAGAAACCCCATCT | 9690 |
rs569196189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179573 | TTTGGTCTCGACATC[A/C]TCATAGGTAGAAACC | 9690 |
rs569203145 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157187255 | CCCTATCTGTAATAT[C/T]TTCTGTAGTACCTTA | 9690 |
rs569207064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240159 | CTCCTGGTTCAAGCA[A/G]TTCTCGTGCCTCAGC | 9690 |
rs569215954 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163123 | GGGCGCGGTGGTTCA[C/T]GCCTGTAATCCCAGC | 9690 |
rs569230894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185825 | ATGTTAAAGATTCAG[A/G]TTTGACAGATGAATT | 9690 |
rs569251173 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169374 | GTCATGAGAGATCCT[-/TT]TTTTTTTTTTTTTTA | 9690 |
rs569259394 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138190 | ATGGGTTTATTGTAG[C/T]ATTAAATACATTTTC | 9690 |
rs569275069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143874 | GACAGGGTGGGACTC[A/G]TGAGGTACTGCAACA | 9690 |
rs569291480 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157221079 | ACGCTGCATTTGAGG[A/G]TGCTGTGTGGGTTGA | 9690 |
rs569292209 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137293 | CCCAGGCTGGAGTAC[A/G]GTGGCACGATCTCAG | 9690 |
rs569312639 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178905 | TGGGGAGTGAGCAGA[A/C/G]GCCAGCCTGCTGCTG | 9690 |
rs569330311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220563 | AGGGGACATGAAGGT[A/G]TGAGGTCAGAGAGAG | 9690 |
rs569340772 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157163247 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGCGCC | 9690 |
rs569348016 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232791 | TTTTCCGAGAAGCAT[A/G]GTGCATGGAGTCGCC | 9690 |
rs569348826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185355 | AAATTATTTACAACC[A/G]TAGAAAATATTACTC | 9690 |
rs569385673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256718 | CCTCGGCATGAGATG[A/G]GATTGTACCAGTGCT | 9690 |
rs569437428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157198998 | TTCACATGGAAAGAT[A/G]TTAATTATAATCTTA | 9690 |
rs569470559 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157251860 | ATTAGAGGGGCTGGG[C/T]GCAGTGGCTCACGGC | 9690 |
rs569503826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168498 | TATATATGAATGTTC[A/G]TAGCAGCCTTAATTC | 9690 |
rs569510288 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157243545 | CCTGCCAGTGGAGTA[C/T]TAGAGTGAGGCCCAC | 9690 |
rs569534642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168056 | TAATATTTAAAACTT[C/T]AAAAAGTCCTGCTAG | 9690 |
rs569552259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140457 | AAGTCACTTGTGCTC[C/G]AGAACTAAGTACTGT | 9690 |
rs569556113 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157246078 | TACTCTAGATGTTTG[C/G]TTTTGGGAAAACCTC | 9690 |
rs569573154 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157174045 | GACAAGGCTATGTGG[A/C/T]GTATTTATGACTAGC | 9690 |
rs569612602 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148997 | GAATACAGTTATGCT[-/A]GTATCCTTTACATGT | 9690 |
rs569615912 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146356 | CCGGCCTCAGCCTAC[C/T]GAGTAGCTAGGATTA | 9690 |
rs569655826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146469 | CTCGTGATCTGCCCG[C/T]CTGGGCGTCCCAAAG | 9690 |
rs569667506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188535 | ACACTTGCTTTTATT[G/T]TCGCACAACCCATTG | 9690 |
rs569690343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232524 | CCAGCTAATTTTTCT[A/G]TTTTTAGAAGAGATG | 9690 |
rs569698596 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174003 | GAAATGTTAATGTCG[A/G]AGAAACTACTTAAAA | 9690 |
rs569710864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176115 | TTTTGATACATGATA[C/T]ATGTAAATATAATTA | 9690 |
rs569712466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189046 | CACAGGACAGTATGT[A/T]GAAGAACCGGCTTTT | 9690 |
rs569741288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158991 | GTCTCATGTATGCGG[A/G]GATATTAAGTCCGTT | 9690 |
rs569741955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264733 | TGCACCACTACAGCC[A/G]GCTAATTTTTTATTT | 9690 |
rs569748386 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157265756 | GCGTGCATTTCATCT[C/G]TGGGAGCACTTAAGA | 9690 |
rs569762572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208403 | TAATTAAGAAAAGTA[A/G]TTTTAGTACTTTTGA | 9690 |
rs569770015 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194176 | GGTAATCTTTTTGAA[A/G]TGGGGCTGGCTGTTA | 9690 |
rs569791784 | snp | C/T | 1.66164e-05 | 0.00288235 | intron-variant | UBE3C | GRCh38.p7 | 7:157248347 | ATTCGATGCTAACGT[C/T]GTCACTGTTCTCTTT | 9690 |
rs569809988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157243310 | GTACGAGCACTGTGA[A/G]GCCTCGGCAGCTCTG | 9690 |
rs569822806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157165921 | GGGTTTCCTTTATAG[A/G]TGACTAGCTGCTTTT | 9690 |
rs569842133 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198760 | GGCTGGTCTCGAACC[C/T]CTGACCTCAGGTGGT | 9690 |
rs569844569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216142 | GATCTGACTCCATTT[A/G]CTTACGTGAGGCAAG | 9690 |
rs569880929 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258723 | CCTCAGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 9690 |
rs569900270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215286 | GTACCCTTCCCCTTT[C/T]TTCTTGGGCACACAG | 9690 |
rs569904228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189822 | TTGTTAGTTTGTGAC[A/G]GAGTCTCTTGCCTTG | 9690 |
rs569955174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254765 | AAACCAGATGGCTGA[G/T]TGCAGTGGCTCACGC | 9690 |
rs569958370 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177701 | CTGCCCAGCCTGCCC[A/G/T]CTGGGTCCTCACCCC | 9690 |
rs569970660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176567 | GGCGTGAGCCACCGT[A/G]CCCAGCCAAACCCAT | 9690 |
rs569971137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157170230 | CTGTAAACACAGCAA[C/T]GTATATTTACATCAT | 9690 |
rs569976587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148042 | TAGGGTGATACTGGC[C/T]TTATGGAATGAGGAT | 9690 |
rs569984521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260114 | TCTTCCAAATTGTTG[A/G]AGAGAAAAAATAACC | 9690 |
rs570027466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233892 | TTCATTACAGCCATT[C/G]TAGTGGGTGGGAATT | 9690 |
rs570131864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157215430 | TTGTGTGATCTTTAT[A/G]ATGTATAATATATCC | 9690 |
rs570144184 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219201 | GAGGAGGGTCTGGTC[C/T]CAGAATGCAAATAGC | 9690 |
rs570160143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195899 | GCACTGTAGTAGGCA[A/G]GAAGAATAATGTTCC | 9690 |
rs570197927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157255501 | AAAAGCAAATAATGC[C/T]TAAGGTCACGTTGTC | 9690 |
rs570219743 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137008 | GTGGCGCGATCTCGG[C/T]TCACTGCAAGCTCCG | 9690 |
rs570241634 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149532 | GTTCATGCACAGGCG[G/T]ACCCTGCACTGGCAC | 9690 |
rs570247806 | snp | A/G | 1.67975e-05 | 0.00289802 | intron-variant | UBE3C | GRCh38.p7 | 7:157223221 | CAGGGGAAAGTACAA[A/G]TGAACTAATTAAGGT | 9690 |
rs570286805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157228158 | CGTTGTCTTATCTCC[G/T]AACGATTCTCTGCAG | 9690 |
rs570309027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183797 | ATGCCTCTCTGCGTG[C/T]GAGGAAAAATGGCGT | 9690 |
rs570313736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209766 | TTAATAATGCCATAT[A/G]AGATATTTTCCACCC | 9690 |
rs570344699 | snp | C/T | 0.00122349 | 0.0247032 | intron-variant | UBE3C | GRCh38.p7 | 7:157190311 | CAGCATCTCTCCCTC[C/T]TAAGAGCCTCCTCTT | 9690 |
rs570439192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176659 | CATGTATTTTTTAAA[A/G]TACAGTGTGTGACAG | 9690 |
rs570446041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221752 | CTAAAAAAAAAAAAT[C/T]TGGCCATTGTAAAAG | 9690 |
rs570477855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182766 | GGTTGGGTGCGGGGG[C/G]GTATATAGAGTCTCG | 9690 |
rs570492572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148881 | CAGCCTCCTGAGGAG[C/G]TGGAACTCCAGGCTT | 9690 |
rs570496481 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181294 | CTTCCAAATGAGTGG[G/T]ATACAGGTGAAATGA | 9690 |
rs570529069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148163 | GTGCCTGGAGTACAG[C/T]GGTGCGATCTCACTG | 9690 |
rs570571252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157259996 | GTTTCAAATAGGTCA[A/G]TCATCGACGCCGTTA | 9690 |
rs570582755 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179042 | TGGCTCCACCCACTC[G/T]GAAAATTCAGAAACA | 9690 |
rs570688498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166493 | CGCCTGTATTCTCAG[C/T]ACTTTGGGAGGCCGA | 9690 |
rs570707134 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242870 | GACCAGCCTGACCAA[C/T]ATGGTGAAACCCCGT | 9690 |
rs570747447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222828 | AGCCTTCTCCCAGGC[A/G]CCATCTCATGCACAC | 9690 |
rs570782325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157228308 | GCACTCCCAGCCTGC[A/C]CTGCACTACCTTGTT | 9690 |
rs570790148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260829 | TTCGAAGTCCTGCCA[A/G]ACGTAGGTTCTAGAC | 9690 |
rs570798891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260729 | GTTTGGAGGACCTGC[C/T]CCCATCAAAACACTG | 9690 |
rs570810610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190756 | TTGGATTATTGATTT[G/T]TGCAGTATCCCCTTG | 9690 |
rs570823793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256072 | TTCAAAATAAGGCTC[C/T]TCTGCAGTAGTTCTT | 9690 |
rs570829190 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201545 | TGGGAGCCGTGTCTC[A/C/G]GTGTCTCATCAAATG | 9690 |
rs570842367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157142750 | TGGTAACTGTGCTCA[C/G]TCCCCGGGTAATGGG | 9690 |
rs570847450 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177489 | CTCTCACATGGGATT[A/C]TCAGCACACATGCTG | 9690 |
rs570864812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267058 | AATGTTATTTATCCC[C/T]TTTTATGCCTGAAGC | 9690 |
rs570880855 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157154076 | TGTAATCCCAGCACC[A/T]TGGGAGGGAGGCCGA | 9690 |
rs570896451 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190350 | TGTTTTGGTGAACAG[A/G]CCCGTCATCTACTTG | 9690 |
rs570951783 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264618 | CAGAGTTTCACTCTT[A/G]TTGCCCAGGCTGGAG | 9690 |
rs570976111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236448 | AATTTCAATTAGATT[A/G]TATAACTTTGGCGTG | 9690 |
rs570980139 | snp | C/T | 0.000947777 | 0.0217483 | intron-variant | UBE3C | GRCh38.p7 | 7:157189010 | TTTCCGAGACAGATG[C/T]GTACATGAAAACCGG | 9690 |
rs571006530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241111 | CTCCCTTCTGTGCCC[A/G]GTGGTTCAAGGGTGC | 9690 |
rs571011894 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202960 | TATCTAAAATATAAA[C/T]ACACTCATCTGCAAT | 9690 |
rs571034121 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262920 | AGTTTGATTCACATT[C/T]GACTACAATGGTTAG | 9690 |
rs571046532 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137324 | CTCATTGCAACCTCC[A/G]CCTCGCAGACACAAG | 9690 |
rs571070338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217522 | CATCTAAAGCAGATT[C/G]AGTAGTATGATACGT | 9690 |
rs571075732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223396 | ACGTATCATATTAGT[A/G]TTAAGAAATTAACAC | 9690 |
rs571083298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177764 | AGAAGGCAGCCTGCG[C/G]TAAGCGGATAAGCCG | 9690 |
rs571089669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137025 | CACTGCAAGCTCCGC[C/T]TCCCGGGTTCACGCC | 9690 |
rs571103244 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252072 | ACCCAGATGGTGGAG[A/G]TTGCACTGAGCCAAG | 9690 |
rs571157459 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157259133 | CAGCAGCTGCAGCAT[C/G]ACTTGAGCACATGTT | 9690 |
rs571187826 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174560 | CAAGTTCAAGTGATC[C/T]TCCCATCTCAGCCTC | 9690 |
rs571188663 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269329 | TTATTTATTTGTATG[G/T]TCTAATGGCTAAACA | 9690 |
rs571206856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157156767 | CAGATTGCTGTACTT[C/T]TCCTGTCCCCCTTAA | 9690 |
rs571215515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157225156 | TACAGGCATGAGCCA[A/G]TGTGCCTGGCCGGAT | 9690 |
rs571217833 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268865 | ACAGAAAGCGTTTCA[A/C]AGCGTCAGCTGTGGG | 9690 |
rs571218340 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157258636 | GGCTAATTTTTGTAT[C/T]TTTAGTAGAGACGGG | 9690 |
rs571250567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157230860 | GTTTGTGGGGGCGGA[A/G]GTTGCAGTGAGCCGA | 9690 |
rs571254017 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162356 | TGTGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 9690 |
rs571257116 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168053 | CTTTAATATTTAAAA[C/T]TTTAAAAAGTCCTGC | 9690 |
rs571263525 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210041 | AAAAATTAGCTGGGC[A/G]TGATGTACGCCTGTA | 9690 |
rs571291438 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212992 | TGAACTCCTAGGCTC[A/G]AGTGATCTGCCTGCC | 9690 |
rs571291744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199591 | TTCTCCTGCCTCAGC[C/T]TCCTGAATAGCTGGG | 9690 |
rs571302663 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237062 | TAAGTTTATTTCTTC[A/C]GAATTAACCATGAAA | 9690 |
rs571310004 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187742 | CCACCTCGCCCGGCT[A/G]ATTTTTTGTATTTTT | 9690 |
rs571335080 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157246930 | GTTTTTGCTCTTGTT[A/G]CCCAGACTGGAGTGC | 9690 |
rs571337425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157164871 | CAGCTGGAAGGGCCT[A/G]TATTAGAGATGGTGT | 9690 |
rs571364835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192903 | TCAAAGAAGACATTT[A/G]AGGTAGTGAATGCCA | 9690 |
rs571374167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164270 | GCTCGGTGATCTTCC[C/T]GCTCTAGCCTCCTGT | 9690 |
rs571394085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157253297 | GTCTGTGTTTCCGCT[C/G]TGTTGCTTTTCTCAT | 9690 |
rs571409612 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143128 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 9690 |
rs571435401 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190880 | TCTTGATCCCATTGC[A/G]CTTTTTTATGCCTCC | 9690 |
rs571436562 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254779 | AGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCC | 9690 |
rs571443291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157214059 | TAACATAACTCCCTT[G/T]GCTGGACTCACTTTT | 9690 |
rs571469792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189085 | AAGGATGGAAAAAAT[A/G]GGAATATATATTCAT | 9690 |
rs571485339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219762 | AAGTTAGCCAGGCAT[A/G]GTGGCATGTGCCTGT | 9690 |
rs571493857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157170837 | AAAATACAAGGTCTC[A/G]GTGTTTACATTTTAT | 9690 |
rs571500232 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152899 | ACAGTGCAGCTTTAA[C/T]GTTGTTTAATTTTTT | 9690 |
rs571526962 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157187766 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 9690 |
rs571531466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157180517 | ATCTTCACTCAAATA[C/T]GAAGCTGTGTAGGAC | 9690 |
rs571533742 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157202098 | AAATTGCTTTGCTCC[-/AT]ATGACTTTACTCCTC | 9690 |
rs571544229 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157158275 | TGAAAACCAGTTTTT[C/T]ATGGACTGGCCGAGA | 9690 |
rs571544445 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214906 | CTGCCTAGGCTGCAT[A/C]AGAAACCATTAATTG | 9690 |
rs571596719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157195231 | AAAGATATGTGAGGA[A/G]CCTCCTGTGTAAATG | 9690 |
rs571634612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194624 | TGGAATGTTAATGCT[A/T]GGGAGGCCTTGAAGG | 9690 |
rs571672423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157247523 | ATGGCAAAACCCCGT[C/G]TCTACTAAATATACA | 9690 |
rs571679328 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266810 | GGTGTGATCATACCT[C/T]ACTAACCTCGACCTC | 9690 |
rs571701734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157247091 | AGACGGGGTTTCACC[A/G]TGTCGGTTGGTCTGG | 9690 |
rs571712554 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157139449 | GCCGAGACTTGGGGC[C/T]GGATTCGGGGCCTCC | 9690 |
rs571749078 | in-del | -/CA | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157224160 | ATTACAGGCATCAGC[-/CA]CTACACCTGGCCTGG | 9690 |
rs571751677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157252319 | ATTTTATACATTGAA[A/C]TATAATAGCTAGCCT | 9690 |
rs571766063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144600 | GAAAAGTTTGTAGAC[C/T]GGAGGAACTGAAATT | 9690 |
rs571801746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152438 | GGAGAAGCACCCACA[C/G]TTGTGCCTGAAGAGC | 9690 |
rs571827856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157152782 | CTGTCTCCTGCTTTA[C/G]TTGTGCATTCCTGTA | 9690 |
rs571849146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157146606 | TACCATACCATCTTG[A/C]TTACTGTAACAGATC | 9690 |
rs571878584 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194333 | AGTTCTGGTAGCACT[C/T]CTGGTATGAAAACCC | 9690 |
rs571885772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145771 | AATAAGCTTTTTTTT[A/T]AGAGTGGTTTACGGT | 9690 |
rs571896018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232701 | TGTTGCTATTGTGAT[C/T]AATTTCTGTAAGAAT | 9690 |
rs571898419 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157259703 | GACACAGAGCGGGTC[-/AG]GGGCTGCACAGGGCT | 9690 |
rs571905271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157242843 | GGGAGAATCACGAGG[C/T]CAGGAGTTCTAGACC | 9690 |
rs571917372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157217242 | ATGATTCTTTGTGAG[G/T]TTGAAAAATATTTTG | 9690 |
rs571933933 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157250708 | GCTGAATTTTCACCA[A/G]TGCAAAATTTAGATA | 9690 |
rs571934787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238327 | TCGTGGGCCTCCTTG[A/G]CTTTGGTGTAAGTAG | 9690 |
rs571949441 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157235021 | ACATGGAGAAACCCC[A/C/G]TCTCTACTAAAAATA | 9690 |
rs571959550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157274 | TACTGAATTCTTAAG[C/T]GAGAAATTTGACTAC | 9690 |
rs571959706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164363 | GGTCTTGCTTTGCTG[C/T]CGAGGCTGATTTCAA | 9690 |
rs571968984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219435 | CATCCCACACCACCT[A/G]GGAAACGTTCTCGCC | 9690 |
rs572005274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157225168 | CCAATGTGCCTGGCC[A/G]GATTTTTAAAATTTA | 9690 |
rs572009304 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157263357 | TTTTGTGCCGTGTCG[C/G]TTTGTGGGCTTGCCA | 9690 |
rs572025235 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157247176 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTGACTA | 9690 |
rs572027744 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167975 | GTCAATGAAAATTGG[A/G]ATTTTCTCTTGAAAC | 9690 |
rs572050816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157258301 | AGTTCCTGCACACTC[A/T]TGTAGTCCCAGCTAC | 9690 |
rs572099156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241891 | GAGAATGTTCTGCCC[A/G]GTGAGAGCAGATGCA | 9690 |
rs572116556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200757 | CTCCTACCTCAACCT[C/T]ATGAGTAGCTGGGAC | 9690 |
rs572134714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157264997 | ATTTTTAATGGGCTT[A/G]TAGTGTCCCATCATG | 9690 |
rs572167845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157180646 | TATTCTATAAAAATG[A/G]AGTAAATGATTCTGA | 9690 |
rs572202633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157180004 | GTTTTAAGACTAAGC[A/G]TTTGAGAATTTGTAT | 9690 |
rs572218497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157751 | AGGCCAAGGTGGGTG[A/G]ATCACCTGAGGTCAA | 9690 |
rs572263883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176811 | GCTCTCTCTGCCCCA[G/T]GCCTGGGGCTGTTTT | 9690 |
rs572270864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168867 | ATTCTAAGATCAGTG[A/G]TGATGGTTGCATAGC | 9690 |
rs572278365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157206856 | GATGGGAGCTGGTGA[A/G]TAAAGTGGACAGTGG | 9690 |
rs572285925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157169607 | TCTGGAACTCATGAC[C/G]TCAAATGATTCGCCT | 9690 |
rs572322438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241466 | TTGGTTCGTGCAAAG[A/G]TGGCCAGCATCACTA | 9690 |
rs572373694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157188759 | ATTTAGAAAGAGCAA[A/G]TAGGCTTACTCTAAC | 9690 |
rs572374369 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169646 | CTCCCAAAGTGCTGG[A/G]ATTACAAGCATAAGC | 9690 |
rs572384090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145335 | CCAGCCTGGTCAACA[G/T]GGTGATACTCTATCT | 9690 |
rs572401750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264526 | CCTGTTACACACACA[C/T]ACACACACCTGGTAT | 9690 |
rs572415172 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157206275 | TTTATTTATTTATTT[A/T]TTTTGGAAACGGAGT | 9690 |
rs572470195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226613 | TCTAAGGAAATGAAA[C/T]CTGATTTCTAATAAT | 9690 |
rs572472583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191044 | TAGTGTTTTAGGGGT[C/T]GAAGAGGTTGATGTT | 9690 |
rs572476948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184182 | ACTACCACAGTTTCT[A/G]GTGATGGGAAAGTCT | 9690 |
rs572544316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157231601 | AGATCATGTGAGCTC[A/G]GCCGTCATGAATGGA | 9690 |
rs572552897 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255232 | CACAATAACGATGTT[C/T]AGCATCATTAGTCAT | 9690 |
rs572571038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215018 | GATTAGTTCACTAAA[C/T]ATTTCCACTCGTTGA | 9690 |
rs572573053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157230223 | CCTTAATTTACTCTT[C/T]GTAGCAAATTATATA | 9690 |
rs572587519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157257338 | ATATTAATAATGTCT[A/C]ATAAATCTGTAACAC | 9690 |
rs572611973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160508 | AAATATATTTAGGTT[A/G]AAAAGAGTCTTTTTG | 9690 |
rs572614091 | snp | C/G | 6.77495e-05 | 0.00581981 | intron-variant | UBE3C | GRCh38.p7 | 7:157220796 | GTTCTCTAGGACACA[C/G]GGTTACTGAGGTATG | 9690 |
rs572620005 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225933 | CAGGCCTTGGCAGTA[A/G]AGCCAGACCCAGTCT | 9690 |
rs572652273 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157247814 | TTTTGTGCTGCAGGG[C/T]AGAGTGGCATATGCG | 9690 |
rs572685471 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157211193 | GAGAGAGAGAGAGAG[A/C]GCCATACTATGAGTG | 9690 |
rs572700778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259687 | GAAAGGCACATTTAG[A/G]GACACAGAGCGGGTC | 9690 |
rs572738845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157266740 | AATCTTGATCCTTTT[A/T]AAAAAATTTTTATAG | 9690 |
rs572742616 | in-del | -/TT | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157244512 | GCAAGACATCATCTC[-/TT]ATATAGTTTTTAGAT | 9690 |
rs572743152 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182949 | AGACGGGGTTTCACT[A/G]TGTTGGCCAGGATGG | 9690 |
rs572745959 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149548 | ACCCTGCACTGGCAC[A/C]TCCCTGAGAGTGAGT | 9690 |
rs572771384 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206573 | GCCTTTTTTCTTTTC[-/T]TTTTTTTTTTTCCTT | 9690 |
rs572781998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154782 | CAGAAGGAGTGGAGA[A/G]GGAACAAAGAAATCT | 9690 |
rs572828765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148393 | CAGGTGTGAGCCACC[A/G]TGCTTGGCCTCAATT | 9690 |
rs572836357 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157184854 | GGGCTTGATTTTTTT[A/T]AAAAAATAAGAGAAG | 9690 |
rs572856455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142533 | AGGATGGGTGTAATT[A/G]GGATGGGTGGAAGAC | 9690 |
rs572860070 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268640 | TCCCATCATCCGCTC[A/G]CCCTCCTTTCCCCTG | 9690 |
rs572863894 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157154285 | AGATCACACCACTGC[A/C]CTCCAGCCTGGTGAC | 9690 |
rs572875044 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157229335 | TGTTTGTTTTTTGAA[A/T]TGGAACTTCTCTCTT | 9690 |
rs572883948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239489 | GCTAGGCATTTTCTG[C/T]GCTGTGGACTAAGTG | 9690 |
rs572905636 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180350 | GTGTATTTTTTAAAA[A/T]TCTTGATGTATTTTT | 9690 |
rs572912598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157178971 | ACTGGTGTCCCAGAC[A/G]CCTTGTGCTCCATCC | 9690 |
rs572913664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234847 | ACACAGCCTACTTCT[C/T]AGTTTCAGCTTCCCC | 9690 |
rs572935116 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157196819 | ACTAAAAATACAAAA[A/G]TGAGCTGGGCGTGGT | 9690 |
rs572936377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157265951 | TTCTGGCACAAGCAA[A/G]CCACTTTTCATCATG | 9690 |
rs572949778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234328 | ATTTTGGTCTTTGAT[A/C]CTTTTTGAGTTAATT | 9690 |
rs572955218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157211765 | ACACTCACAGTATTC[A/G]TCCCACCCATAGTGA | 9690 |
rs572977165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157178552 | ATGATTTCCCTGTCT[A/G]TCTGTAAGATGTCCC | 9690 |
rs573040602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157263583 | GCAAGAGAATTGCTT[A/G]AACCTGGGAGGCAGA | 9690 |
rs573051675 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137841 | AGTGCTGGGATTACC[A/G]GCGTGAGCGACCGTG | 9690 |
rs573052928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157223689 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCG | 9690 |
rs573059627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157262044 | AAAATATATTTTAAG[C/T]TTTTCATTTATCCAG | 9690 |
rs573087704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178402 | ATACTTCTTACAGTG[C/T]TTTGTAATCTTTAAT | 9690 |
rs573097294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157144170 | GGATGCTGTGGCGCA[C/T]GCCTACAATCTGCCA | 9690 |
rs573118078 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157249873 | GTGCATCCATAATCT[A/G]AAAATCCAAAATGTT | 9690 |
rs573135668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230419 | AAAAAATTACAGGCC[A/G]GGCACGGTGGCTCAC | 9690 |
rs573140856 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160767 | TACATTAGTAGATCT[C/T]GTCTGCAGTGTTTTT | 9690 |
rs573142786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142850 | ACTCTAAAATAAAAG[C/T]TGAATTTTTTTTTTT | 9690 |
rs573173885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157236047 | TTACTGTGATAAAGT[A/G]CAAAGAGGTCTTCAA | 9690 |
rs573196627 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157144967 | ACAGCGTTATACAGA[-/AG]AGTGTCATTGCCCTA | 9690 |
rs573205640 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153372 | AAAAAAAAATAGTTA[A/G]CTCTGGAACCAACTG | 9690 |
rs573211153 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157172146 | AAGCGATTCTCCTAC[C/G]TGAGCGCCCTGAGTA | 9690 |
rs573220084 | in-del | -/AAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163402 | TCAAAAAAAAAAAAA[-/AAAA]GGAAAGAAATGATAC | 9690 |
rs573226667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157230857 | AGAGTTTGTGGGGGC[A/G]GAGGTTGCAGTGAGC | 9690 |
rs573255555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157178472 | GTGAACTTAGTGCCA[C/G]CATACCGTTTGGCAC | 9690 |
rs573280273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157173529 | CAAAAATCAACATAT[A/G]TGGCTATTTCTTCCT | 9690 |
rs573337853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157262089 | GTCACTGACCCCTTC[A/G]TTCAGAGATCCTTTT | 9690 |
rs573347567 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245820 | ATATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 9690 |
rs573351570 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157250691 | TTTTTCCATACCATA[C/G]AGCTGAATTTTCACC | 9690 |
rs573361874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167714 | GCTAATTTTTTGTAT[C/T]TTTAGAAGAGGTATG | 9690 |
rs573377345 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189400 | TTAAATATTCACTGG[C/G]TATATTTTAAGGGGG | 9690 |
rs573391902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150724 | GTAGATTACAAAACA[A/G]GATTGCAGTCTGCAT | 9690 |
rs573445998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157186622 | AGGCAAAAACCGGGT[A/G]TTCAGAGTTTACTGT | 9690 |
rs573454663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157150033 | GCTGTTGCTGAGGGC[A/G]TACAGACACTGGGCA | 9690 |
rs573464770 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268588 | TTTGAACCAAAGTGG[C/T]GGCTGCATCTTTGTC | 9690 |
rs573472000 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207273 | CCTTGCCTTTAAATA[C/G]TTTAATTCCTAATGC | 9690 |
rs573502826 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268933 | TCTAAATCCTCATTT[A/G]TCTCTTCTATGTCTC | 9690 |
rs573511670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157185567 | TCTTTCTTTGCCATG[C/T]CTCTTACCTGTATGT | 9690 |
rs573524304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157191889 | AGAAGTAAATTTTGT[C/G]TATAATTTCATAGCT | 9690 |
rs573547713 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157161070 | TAAGAAGAAATAGTA[C/T]CTAAATATAATGTGG | 9690 |
rs573555904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157143449 | CCACCACAGGAGTTG[C/T]TTGTCTTTCTCCAGG | 9690 |
rs573579670 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157173704 | CCAACAGTCCTATTA[C/T]ATAATGTATAGTTAT | 9690 |
rs573583972 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184579 | CCAATGACTTTTTTT[A/G]GTCTTAAGCAATTGA | 9690 |
rs573591982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149833 | ATTTGGAAGTGGGGC[A/G]TCTTATTCTTTGACT | 9690 |
rs573613970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179161 | GTCTGCAGTGCAGCT[C/G]CCGGTCCTTCACCTG | 9690 |
rs573650561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191527 | AACACCTGGGCCCAA[A/G]TAATCTGCTTGTCTC | 9690 |
rs573653425 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158523 | AAGCTGCTGCCAAAG[C/T]TGTGATTAAAAGTGA | 9690 |
rs573671508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199883 | TATTACCATTTTTTC[A/G]TTTTTCCAATATTAT | 9690 |
rs573671844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157184957 | AGCCGTTTTTATAGT[C/G]GACAGTGGATGCTGG | 9690 |
rs573676415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157224041 | TGAGACAGGATCTCA[C/T]TCTGTCACCTGGGCT | 9690 |
rs573683968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177258 | ATTACTAATGATGAC[A/G]GGTGTTTCTCAGGAG | 9690 |
rs573686444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157234981 | CGGATCACCTGAGGT[C/T]GGGAGCTCGAGACCA | 9690 |
rs573722559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191347 | CCCAGGCTGGAGTGC[C/T]GTGGCGTGATCTCAG | 9690 |
rs573747767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157229380 | AGTGCAATGGCACAA[C/T]CTTGACTCACTGCAA | 9690 |
rs573752801 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160106 | CTGAGATGGAGTCTC[A/G]TTCTATCACCCAGGC | 9690 |
rs573782419 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245958 | ATCGTGCCACTGCAC[A/G]CTCCAGCCCGGGCAA | 9690 |
rs573811553 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157144543 | AGCAGGCAATGGGAA[A/G]TATTTTGAGACTTAA | 9690 |
rs573821468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157167730 | TTTAGAAGAGGTATG[A/G]TTTCACCATTTTAAC | 9690 |
rs573850273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157256837 | TTAGTTTCCGTGGGT[G/T]TCTGGACCAATCCCT | 9690 |
rs573885273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157250736 | ATAATTTGGCGGGGG[A/G]GCTGTTACTGTCATT | 9690 |
rs573891834 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157225824 | GATGTGTTAGCGTGC[C/T]CCTGTTGTCCCTGCT | 9690 |
rs573931017 | in-del | -/TTA | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157234034 | TTATTGGATTGTCTT[-/TTA]TTATTAAGTCCCTGC | 9690 |
rs573945140 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138372 | TATGAGGCAAATCTG[C/T]GCATGTCTGTGTACA | 9690 |
rs573951527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157192544 | TACTGTCTGACTACA[A/G]CATTCAAAAGGAGCT | 9690 |
rs574015424 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233905 | TTCTAGTGGGTGGGA[A/G]TTGGTATCTCATTGT | 9690 |
rs574021522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157236148 | TGATTCTTGCTTCTG[C/G]TGTGGGTCATGATTG | 9690 |
rs574053959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168148 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 9690 |
rs574063591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157202472 | AACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 9690 |
rs574074150 | snp | A/C | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231118 | CGTGTGCACTTGCTC[A/C]ATGCCCATGGCCTGG | 9690 |
rs574101974 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268636 | GGTCTCCCATCATCC[G/T]CTCGCCCTCCTTTCC | 9690 |
rs574151067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157139467 | ATTCGGGGCCTCCCT[A/G]GCGGGGACTCGGGGC | 9690 |
rs574164486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246261 | GATTATTACTAAATA[C/T]GGTAACTGGTTGGAA | 9690 |
rs574165078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157144660 | GGGAGTAGAATTAAG[A/G]TCACTTTAATGTTTG | 9690 |
rs574201658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157240850 | GAACTGGTAGCTAAG[A/G]TGGAGTTGAGGGACA | 9690 |
rs574213095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157258461 | CTGTTTTGTTTGTTT[C/T]TTTGTTTTTGAGACG | 9690 |
rs574218796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230990 | CCTAAGATCCTCACA[A/C]CCCTTCCTTAAGCCT | 9690 |
rs574236784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208705 | ATTTTAACATATCTT[A/C]GTTCTTAACCAGAAA | 9690 |
rs574281959 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157230509 | AGACCAGCCTGGCCA[A/G]TATGGTGAAACCCCA | 9690 |
rs574287845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222196 | TTTTTTAGTTATTGA[A/C]TTTTGAGAGTTATAA | 9690 |
rs574321537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264220 | TATTACAGGGGTGCG[C/G]CAACATGCTCGGCCT | 9690 |
rs574335685 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157151397 | GGTGAATGTGAGTTC[A/G]CTCGGAGAAGATTGT | 9690 |
rs574388369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157238779 | ATGAAGAACTGAGCC[C/T]CAGGGCTCTCCAAGG | 9690 |
rs574436358 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219943 | CAGCCGGGTGTGGTG[A/G]CTCACGCCTGTGACC | 9690 |
rs574440373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE3C | GRCh38.p7 | 7:157243489 | TGCTGAATGAGGAGT[A/G]AGTTCACCTCAGCTC | 9690 |
rs574459721 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229949 | TTTTTGAGACTGTCA[-/C]GCAGGTTGGGATGCA | 9690 |
rs574460323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165538 | GAGTAGCTGGGACTA[C/G]AGGTGCACGCCACCG | 9690 |
rs574494610 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137046 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 9690 |
rs574523792 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157218448 | AGCAAGATTCCGTCT[C/G]AAAAAATAAAAAAAA | 9690 |
rs574549972 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157222922 | GGTGGCCAGGGCACC[A/G]CCCACTGCTGGATCT | 9690 |
rs574602331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243052 | AGAGGGAAACTCCAT[C/T]TCAAAAAAAAAAGGA | 9690 |
rs574610402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157147797 | GTATCTGTTAATGTT[A/T]TGTGATTTTCCTTCT | 9690 |
rs574618990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157147042 | CTTTTGCCTCTCCAT[A/G]AGAGTCAGTTTGTTG | 9690 |
rs574640658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183495 | CTTCTTCTCCAGTGT[C/T]CCTCCCACAGACAGC | 9690 |
rs574645222 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207766 | TGATAATGTTGTCTC[A/G]ATGCCTTCGAGATGC | 9690 |
rs574657104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153297 | TATGGTTCACATCAC[A/T]TCTTGCCACTGTGAA | 9690 |
rs574690669 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197986 | TAGGTTTTATGTATT[C/T]TTGATCCTGATGGTC | 9690 |
rs574691080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157202568 | AGGCTGAGGCAGGAG[A/G]ATCGCTTAAACCTGG | 9690 |
rs574719427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154392 | TGAATCCCCTAACTT[C/T]CCACCATTATTTTCT | 9690 |
rs574737065 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240655 | CAAGAGCCTGCCTTT[G/T]AATCTAGGCTGTTTA | 9690 |
rs574756105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153812 | CGAGATCCCGTCTAT[A/G]CTAAAAATACAAAAC | 9690 |
rs574756469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157160615 | ACTGAGCCAGTTGAT[A/G]TCTTAGTTGGTGTCT | 9690 |
rs574763459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210155 | GCACTCCAGCCTGGG[C/T]GGTAGGGTGACTCTC | 9690 |
rs574772571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249746 | ATGGACATTTGGGTT[G/T]TTCCTATGTTTGGGC | 9690 |
rs574777617 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261710 | TTATGAAACTCCTTA[A/G]TGCCAGATTATTGGA | 9690 |
rs574796117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157217190 | AGTTATTAATCCTCA[A/G]TTTTCCTTTTTAACC | 9690 |
rs574801699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216688 | GTTGGCAGATAACTG[A/C]TTTGTATACATTATT | 9690 |
rs574804091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157142370 | TAGATCTGTGTACGA[C/T]AAGTCTGACTTGAAG | 9690 |
rs574808942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255073 | CTCAGTGAGCCGAGA[A/T]CATGCCACTGCACTC | 9690 |
rs574810668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157244560 | ACTTTAGAGCTGCCT[A/G]AAGATTGATAGAGAT | 9690 |
rs574816951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224490 | TGAGCCACCGCGCCC[A/G]GCCACTTTACTTTTT | 9690 |
rs574817305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171963 | CCACCTGCCTCGGCC[A/G]CCCATAGTGCTGGGA | 9690 |
rs574856128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190057 | CTCCCGCCTCAGCTT[C/T]CCAAAGTGCTGGGAT | 9690 |
rs574885203 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157255673 | TTAAAATATTATATT[C/G]ATTTTGGTGCCAATT | 9690 |
rs574922582 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157211087 | AACTTAACAGGAGTT[-/A]TCCTCCTGTGATAGG | 9690 |
rs574931776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239929 | TCTGGGTGATGCAGC[A/G]GAGAGCAAGGATGGG | 9690 |
rs575001885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177416 | GAGCTACATCCTATG[C/T]TGTCTCTCACACGAG | 9690 |
rs575057044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197595 | CTGCATGGATAGGAA[C/G]AATATTATTTTAGTT | 9690 |
rs575057138 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243059 | AACTCCATCTCAAAA[A/C]AAAAAGGAAGCGTCA | 9690 |
rs575067502 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167315 | TCCCACAGTGTGTGT[C/G]TTAGTCTCAGCTTTG | 9690 |
rs575089355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157217267 | ATTTTGCTTTTATTA[A/G]TATTAATATATGTCT | 9690 |
rs575089365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157223580 | TGAAAGCCAGTAAAC[A/G]CTATAGATTTCTTAT | 9690 |
rs575126668 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222948 | GATCTGGCTGCATTC[A/G/T]GGCCTCACCGCCAGT | 9690 |
rs575142084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157202872 | TTGTAGGGCAAGAGT[A/G]TAGAAAGTGGTCTTG | 9690 |
rs575153083 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157218855 | GAAAACAGCTAACTC[-/T]TGAGTTCGCAAGGGT | 9690 |
rs575158349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157160360 | GATTACAGGTGTGAG[C/T]CCCTGCAGCAGCCAC | 9690 |
rs575187268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157190398 | CCTGAAACTGCAGTG[G/T]CCTGCATGGTAGCCA | 9690 |
rs575265742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157240274 | TGGCCAGGCTGGTCT[C/T]GAATTCCTGGCCTCA | 9690 |
rs575288895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157217673 | AACCCTGTATCTCTA[C/T]TGAAAATACAAAAAT | 9690 |
rs575301636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157154181 | CAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCGGC | 9690 |
rs575303663 | in-del | -/TTTC | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157146244 | ATTTTTATGGATCTA[-/TTTC]TTTTTTTTTTTTGAG | 9690 |
rs575304569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157166154 | TTGCTTTATGTTATC[C/T]CAAATGTCATGAATG | 9690 |
rs575335605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202535 | GGTGGTGCGTGCCTG[G/T]AATCCCAGCTACTTG | 9690 |
rs575341231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157267155 | TGGGCCAGGCACGGT[A/G]GCTCACGCCTGTAAT | 9690 |
rs575393516 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137078 | AGTAGCTGGGACTAC[A/G]GGCGCCTGCCACTAT | 9690 |
rs575424925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157149987 | TAGCCCATCACCTTC[A/G]ATGGTGGTCAAATTA | 9690 |
rs575431442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243997 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGATCAC | 9690 |
rs575433350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157239073 | TGTCAGGATTATCTT[C/T]CTAAAGCATCATATT | 9690 |
rs575498641 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157234122 | AAATGATTTGCAAGT[A/G]TTTTCTTCTCTGGAT | 9690 |
rs575506059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157260873 | ACTAAAGAGCCAGCA[A/G]TAACGTGTGCCTAGG | 9690 |
rs575546672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255767 | ACAGCAATTATTTTA[C/G]GTTTAGGGAGCACTT | 9690 |
rs575563230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157148338 | GAACTCCTGGCCTCA[A/G]GTGATCTGCCCACCT | 9690 |
rs575572928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204107 | GAATGGGAATCACCT[C/T]TGACCATCTTGAAGT | 9690 |
rs575598630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157250633 | TGTCCAAGAGCCATA[C/T]TTATTTGGTTACAAC | 9690 |
rs575600677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157210201 | AGGGTGAAAATTTAC[C/G]TTTTTTTTGTTGGTG | 9690 |
rs575622878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249254 | GCTCCCCCACCTCCC[A/G]CAGGCAGCCACCAGT | 9690 |
rs575632831 | snp | C/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174967 | TCTCTGTTTGTCAAG[C/G]AGTTGGATGGATCTG | 9690 |
rs575674974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157239620 | GGATCGGAGAAGAAT[C/T]GGGGGACTGGTTATC | 9690 |
rs575691523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157219957 | GGCTCACGCCTGTGA[C/T]CCGGGCACTTTGGGA | 9690 |
rs575702233 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245632 | TAATTGGGTAATCAT[C/T]AGTCCTCAAATCAGA | 9690 |
rs575703164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157249781 | AAGAATATTACTGTT[A/C]TAAACATCCACATAC | 9690 |
rs575780021 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205226 | GCATTGGCACATATC[C/T]TTGCCAATCCCAGTT | 9690 |
rs575786862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172944 | GTCTTGCTTCAGAAG[C/T]CATCTGTGAAAAGCT | 9690 |
rs575794178 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146057 | ATTTTACATTTAGGT[C/T]TCTGATCCATTTTGA | 9690 |
rs575816116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157162218 | TTTCTTTTTTGAGAC[A/G]GAGTCTTGCTGTGTT | 9690 |
rs575829535 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217855 | AAAAAGAAAGAAAAA[C/T]GAAAGAAAATACAAA | 9690 |
rs575831530 | in-del | -/AAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193277 | TAATATTTTTTTAAA[-/AAG]AAAAATTTCAGAAGA | 9690 |
rs575832656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157245542 | TTTACATTATCAGGA[A/G]ATGATGACTATGTGC | 9690 |
rs575858037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157158418 | CAGGTTGAAAGTAGA[G/T]GCACAGAGTGGCAGG | 9690 |
rs575860108 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157152215 | GGACAGAGCTGGGAG[A/G]AAGGTAGTCAGGGAG | 9690 |
rs575867437 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228354 | GGGAGAAACCGTCAC[A/G]TTCCCTCATGGGATT | 9690 |
rs575870549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157191679 | ATGAATGCTCTTTAG[C/T]TCTGAGAGATTTATA | 9690 |
rs575887874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157204808 | GTAGGTGCTGGTGTT[C/G]GCTGTTTGATAAATA | 9690 |
rs575895653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157968 | CTGGGCAACAGATAT[A/G]TATAGATATATATAT | 9690 |
rs575899867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157161102 | GTCCTGGATAGGATT[C/T]TAGAACAGATAAACA | 9690 |
rs575915022 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157241957 | TGTCCAAAACAGGAA[A/G]ATCTAGAGACAGAAG | 9690 |
rs575951743 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157242525 | AGTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTAAA | 9690 |
rs575951784 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214373 | GAATAGAAATAGATA[C/T]CTAGGAGTTAGGCAG | 9690 |
rs575970648 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157214300 | GAACTTAATTGTCTC[A/T]TATAATTTGATAATG | 9690 |
rs575979954 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254947 | ACCTGCAGTCCCGGC[A/G]TGGTGGCGTACACCT | 9690 |
rs575980012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176296 | TTTTTATTTTTGAGA[C/T]AAGAGTCTTGCTCTG | 9690 |
rs575997308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157169700 | TTTGTTTTTTGTTTT[C/T]TGAGAGAGTCTTGCT | 9690 |
rs576026319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259396 | TCAATGTGATGTCGC[A/G]GCCCCACCGTTGGGA | 9690 |
rs576041374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157213610 | AAAGTGAATGTGGAA[A/C]AAAGGAATGTGTTAA | 9690 |
rs576046043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197686 | GCTCTTTATTCGGAA[A/G]TGAAGTCACAAGAAT | 9690 |
rs576060883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157259732 | GCTGGAGGTGGCAGC[A/G]GGAGCTTCGGAGAAG | 9690 |
rs576063597 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157253027 | GTGAGCCACTATACC[C/T]GGCCTGTTTTTTTGG | 9690 |
rs576063856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168941 | AGAATGAATTTTATG[A/G]TATGTGAATTACATA | 9690 |
rs576079282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153078 | GTGGGCGCCTGTAAT[C/T]TCAGCTACTTGGGAG | 9690 |
rs576104740 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157181359 | GTTTGTATACCGTTC[A/G]GCTGCCTATATATTT | 9690 |
rs576175065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157258766 | TGCCCGGCCCCCCAA[G/T]TATTTTTTTATATTT | 9690 |
rs576185376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157175476 | GCATAAGCCACTGCC[A/G]TGACTTTCTTGCATT | 9690 |
rs576185683 | in-del | -/AAAAG | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157247700 | CCGTCTCCAAAAAAA[-/AAAAG]AGCATAAGTAATATT | 9690 |
rs576218768 | snp | A/G | 0.000774281 | 0.0196606 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174969 | TCTGTTTGTCAAGCA[A/G]TTGGATGGATCTGAG | 9690 |
rs576233644 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259632 | AAGACACAAGACTAC[A/G]TATTATTATATGTAA | 9690 |
rs576250978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157164991 | TCTTTGTTGGGGGGA[A/G]CTGCTCTGTACATTG | 9690 |
rs576251719 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157235443 | CCTGAATGTATAAAT[C/G]ATCCAGTCTTGATTA | 9690 |
rs576278210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194803 | TTGTGTCCTGCAGTT[A/C]TGTGTAAAGCAGAAT | 9690 |
rs576287939 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251446 | TTAGGTAGAAAAGAT[G/T]GGACTTGAGTCACGA | 9690 |
rs576315421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157194263 | GAATTCCTCTAAATT[A/C]TGGCACTGAGAAAAC | 9690 |
rs576333024 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157207639 | GTTTTAAGCTTTTTA[A/C]GTCTTTCAGTGTGTG | 9690 |
rs576338969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157182862 | CAAGTGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 9690 |
rs576370449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140799 | AGTGAGATTTCTTAA[C/G]TGTTGATCAGAATCT | 9690 |
rs576371977 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189582 | ACCCTACTTACATGT[A/G]GATGAGGCCTGCGGT | 9690 |
rs576410532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157208601 | TTCACTAAATATTTC[C/T]TAGATTTTATTGTTT | 9690 |
rs576427518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157226755 | ATTTACCGTTGCCAT[C/T]GAATCCTTGCCATGG | 9690 |
rs576447494 | snp | A/T | 3.30759e-05 | 0.00406655 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207861 | ACAGCATTTCAGAGT[A/T]TTGGAGTTACTACTA | 9690 |
rs576450470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157232905 | TTAAAATATAACTCA[C/T]ATTATGGAAAATTGA | 9690 |
rs576471011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157189238 | CACTTTTAAGTTTTG[C/G]ATTAGGTGAATGACT | 9690 |
rs576486655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157188839 | TGAAAGATGATTAGT[A/G]TATTCCCAGGCTGAT | 9690 |
rs576535659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220845 | TCACTCCTTTAATCT[A/G]CAGATCTGTTATTTT | 9690 |
rs576542590 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244904 | CTTCTAGGAACAAGC[A/G]TGGTACAGCTGGCTG | 9690 |
rs576603054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157165639 | CCTAACCTCAAGTGA[G/T]CTGCCTGTCTCAGCT | 9690 |
rs576625190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157248718 | TGTGAGTTAGACGTC[A/G]AAGCATATAGCTCCA | 9690 |
rs576656178 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221910 | GGGTCTCACTGTGTG[C/T]TCAGGCTGGAGTGCA | 9690 |
rs576696465 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250247 | TTGAGACGGGGTTTC[A/G]CTCTGTCACCCAGGC | 9690 |
rs576701746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238426 | TGCTGCCCATGTCCC[A/G]GTGGTAGTGCTGGTA | 9690 |
rs576720494 | in-del | -/ACTCAGAAAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216251 | ATTATTTCTCAGAAA[-/ACTCAGAAAT]ACTCTTTCAGGAAAA | 9690 |
rs576725322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157216409 | AGTTTTGTTACATAG[A/G]TAAACATGTCATCGG | 9690 |
rs576738619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157238118 | TTTAATTTAGATTTA[G/T]ATTTAGCAAATGTAA | 9690 |
rs576757802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243115 | TATTGTGGCTCGATC[G/T]CTGGAAGCCACTATG | 9690 |
rs576762183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157215647 | TTCTGTGGTGATTTC[C/T]GTTGTCTTTAATTAG | 9690 |
rs576764069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221956 | CTCACTGCAGCCTTG[A/T]CTTCCTGGGCTTCAG | 9690 |
rs576781975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157255172 | GCAAAAAAAACCAGA[C/T]GTTTAACATAGAAGA | 9690 |
rs576812558 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259706 | ACAGAGCGGGTCAGG[A/G]GCTGCACAGGGCTGG | 9690 |
rs576834924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157141716 | GACTGTCCTTCTGAC[C/G]TCCATTACTGTAGAT | 9690 |
rs576865670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157254981 | GTCCCGGCGTGGTGG[C/T]GTACACCTGCAGTCC | 9690 |
rs576894321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157176194 | TGAAGCCCAGGAGTT[C/T]GAGGCTGCAGTGAGC | 9690 |
rs576916210 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257080 | TTGCTTTAAAGACCA[C/T]TTCATAATAAGAAAG | 9690 |
rs576925384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157233383 | CCTGCGCTTAAGGAG[A/G]CCTCCTGCTTTCAGC | 9690 |
rs576927556 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150774 | ACAGTAAAGATAGCT[A/G]GTTTCCCAGTTTCTT | 9690 |
rs576927796 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177718 | TGGGTCCTCACCCCC[C/T]GTCTCTCCTGGGCTT | 9690 |
rs576978359 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224181 | ACCTGGCCTGGAAAC[A/G]CTACTTTATTTTTTT | 9690 |
rs576996257 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195814 | TTGAGCACCTATGAG[C/T]GACGTAAATTTATTT | 9690 |
rs577036448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157169807 | TGCCCCAGCCTCCTG[A/G]GTAGCTGGGACTACA | 9690 |
rs577066734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157160009 | TACCTTGAGGAATCA[A/G]GTTTCAGATAGGACT | 9690 |
rs577083690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189463 | AACTAAAATAAGAAA[A/G]TAGGCTACCAAAGAT | 9690 |
rs577097035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157255611 | CATTACCCATCTGCA[C/T]TGAGGGCTTGCACCT | 9690 |
rs577104782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157166371 | CTTTGGTAAGTTGCT[C/T]ACTTATATCCTGAAT | 9690 |
rs577135994 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157248974 | TCCAGCACTGTCTAG[C/G]GGGTGTGTTCATTAC | 9690 |
rs577194935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157222069 | AGAGATGGAATCTCC[A/G]TGTGTTGCCCAGGCT | 9690 |
rs577219756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157165480 | TCAGCTCACTGCAAC[C/T]TCCGCCTTCCAGGTT | 9690 |
rs577231429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157227731 | AACTACTCCCTGTAG[A/G]TGATTTTTTGATGTT | 9690 |
rs577232291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157221517 | GGAGGCCGAGGTGGG[C/T]GGATCATCAGGTCAG | 9690 |
rs577236460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265792 | AAGCGTTGGTTGCCA[A/G]TGGGAATGGGAACTG | 9690 |
rs577252372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157257505 | TAAAATTGCCTCAGG[C/T]AGATGGATCATTTGA | 9690 |
rs577265769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157176941 | TTATCTGCCACGTGC[C/G]AGAACATTGAATTTT | 9690 |
rs577272720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157260240 | TAGAATGAGAGAAGC[C/G]TGAATGTTACAACAG | 9690 |
rs577273018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157143525 | GCAGACTGGCTTTCT[C/G]CATTTCTCACACATG | 9690 |
rs577283137 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157227013 | TACATTGTATTTTTA[-/T]TAGCAGATTTCACGT | 9690 |
rs577289232 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165438 | AGTCTCACTTTGTCA[A/G]CCGGGCTGGACTGCA | 9690 |
rs577302109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216456 | CCTTAGATCACTCAG[A/G]TATTAAGCTCGGTCC | 9690 |
rs577319392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157244013 | GAGGCGGGTGATCAC[C/T]TGAGGTCAGGAGTTC | 9690 |
rs577350079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157202929 | AAGAAAGAATTTTTG[G/T]TGGGTTGGGGTGGTA | 9690 |
rs577413112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157183454 | TGTGTTGAGCTCATT[A/G]TGTCTTCCTGTTGAG | 9690 |
rs577450159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157182996 | TCGTGATCCACCCGC[C/T]TCGGCTTCCCACAGT | 9690 |
rs577453007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157172436 | AATAAGTCTTCCTCG[C/G]TACAAACCATCCCTA | 9690 |
rs577483521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157243593 | GGAGCTTGGTGTCCT[C/G]CTGCTGCTGTTCCTG | 9690 |
rs577488951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157171907 | AGATGGGATGTCGCC[A/G]TGTTGGGCAGGCTGG | 9690 |
rs577492285 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157174827 | TTTGATTAAATGTGC[A/C]TTGCCACTAAAGGAA | 9690 |
rs577494107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157168183 | GGTGAAACCCCGTCT[C/G]TACTAAATATACAAA | 9690 |
rs577530331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157174239 | TGGTGGCGGGCACCC[A/G]TAATCCGAGCTACTT | 9690 |
rs577530801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157210049 | GCTGGGCGTGATGTA[C/T]GCCTGTAATCCCAGC | 9690 |
rs577552179 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140730 | GGCAGGAACACCCCA[C/T]GGGCCACGGATGTTG | 9690 |
rs577562276 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138802 | ATGGCGGAGGCGCGC[A/C]CGTCTGCAGGGCCGC | 9690 |
rs577567244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157209595 | TTCCTTTCAATATTT[C/G]ATTAAACCCTGGGGT | 9690 |
rs577581000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193989 | ATGTGCATCTATAGG[C/G]ACTGAACTGATATGA | 9690 |
rs577592132 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157224651 | AAAGATTACTTGGTT[C/G]CGTTCTTCAGTAATG | 9690 |
rs577610774 | in-del | -/T | 0.190519 | 0.242821 | intron-variant | UBE3C | GRCh38.p7 | 7:157187584 | TGTGTTTGTTTTTTG[-/T]TTTTTTTTTTTGAGA | 9690 |
rs577616211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157193271 | GTCCAGTAATATTTT[A/T]TTAAAAAGAAAAATT | 9690 |
rs577630073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157230274 | TTCAGCCAAATACAG[C/T]TTTTAAAAGATCACG | 9690 |
rs577632246 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268427 | GGTGGGGACTTCATT[A/C]ATTGTCCTATTTCTA | 9690 |
rs577666196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157179167 | AGTGCAGCTGCCGGT[C/T]CTTCACCTGACCAGG | 9690 |
rs577709760 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222328 | GAAGTTTTAAATTTT[C/G]ATAGAATCCCATTTA | 9690 |
rs577809267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157246796 | TCTAAAACTGTTCTC[C/T]ACCTGTTCTCCACAC | 9690 |
rs577842239 | in-del | -/AG | 0.00517822 | 0.0506191 | intron-variant | UBE3C | GRCh38.p7 | 7:157220571 | TGAAGGTATGAGGTC[-/AG]AGAGAGGGCCCAGCC | 9690 |
rs577842629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251604 | TGGTGGTGTCTTGTG[A/G]GGCTTTATGGATTCC | 9690 |
rs577867064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157197751 | ACAATAAAGTTCCGG[A/G]CATCCAGGATCCTGT | 9690 |
rs577901989 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267820 | AGCAGCGCCTCCCCA[C/G]ACCCACGAGGATACT | 9690 |
rs577902385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157149095 | GAGTTTTGCTCTTGT[C/T]GCCCAGGCTGGAGTG | 9690 |
rs577906816 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154533 | CATATCGGCATCTTT[A/G]TATTTGTTATTTTTC | 9690 |
rs577918206 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142259 | ATTATTTGAAATCTT[-/C]CCTTTCTGGAGCTTA | 9690 |
rs577925149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157213310 | CACTGGTTCTCAAGT[C/T]GTAACTACCTATCAG | 9690 |
rs577953847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157187869 | ACATGAGCCACCACA[C/G]CCAGCCTTCATAGTA | 9690 |
rs577961137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157212543 | AACTCTCAAACATAG[C/T]GATCTTGTGAAAACA | 9690 |
rs577965257 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269106 | AATAATAAATTAAGC[A/G]TTTAAATGCTATTTG | 9690 |
rs577972242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157200721 | CTCACTGCAGCCTTG[A/G]ACTCCTGGGCTCTAT | 9690 |
rs577992441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157157688 | CCATTAAAATATAAC[A/C]TGGTGGCTGGGCGTG | 9690 |
rs578062838 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234966 | GGAGGCCTAGGCAGG[C/T]GGATCACCTGAGGTC | 9690 |
rs578066017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241828 | GGACTATTACTGGGC[C/T]GTAAAAAGGGGTAAA | 9690 |
rs578066441 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157190972 | GGCATGTTCTCAGGG[A/G]CTTGGCTCTTTTACC | 9690 |
rs578066758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157199908 | TATTATTAAATATTT[A/C]TTATTAAGTAATATT | 9690 |
rs578113315 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146507 | ATTACAGGCATGAGC[C/T]CCTGCGTCCGGCCTT | 9690 |
rs578115091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157220619 | CCAGCACCAATTCTG[G/T]TCAAGTGTGATCAGG | 9690 |
rs578116051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157140173 | GCCCCTCCCTTCCCA[C/T]CCCTTCCCATCATTT | 9690 |
rs578134073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157241382 | TATATATGAAGGACT[C/G]CATGATAAAAATGGG | 9690 |
rs578160431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157225989 | TTTGGGAGACATGTT[A/G]TCAAGTAATATTTCT | 9690 |
rs578163393 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157264270 | ACACCTGGTACTACA[C/G]GTGTAAGCCAACATG | 9690 |
rs578199909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157264903 | TAATTTTAGCTGTAT[A/C]TTGTGTTCAGTTTTC | 9690 |
rs578234884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157259349 | TACCCCCATTTTCAA[A/G]GGGTGCAGGCAAGTT | 9690 |
rs578234964 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157253069 | AATACTTTTTAAAAA[A/T]TTTTTTATTTAAAAT | 9690 |
rs578238530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157145268 | AAAAGGAGGAGGCCC[A/G]GCACTTTGGAAGGCC | 9690 |
rs578250741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157231483 | GAAACAAATTTGTAT[A/G]GTTGTAAGTAGGTGC | 9690 |
rs745308480 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209941 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGTG | 9690 |
rs745308907 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221543 | GTCAGGAGTTCAAGA[A/C]CAGCCTGACCAACAT | 9690 |
rs745338974 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248373 | TCTTTTGAAGGCTCT[C/T]TATGAGAACATGCTG | 9690 |
rs745356861 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244620 | TTCTTAATGTAGTAA[A/G]TTACTGAAGTTATTT | 9690 |
rs745376844 | snp | A/C | 1.65386e-05 | 0.00287559 | intron-variant | UBE3C | GRCh38.p7 | 7:157169024 | CTGACCAATTGCTCC[A/C]TCACTCCTCCTTTTA | 9690 |
rs745428984 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152632 | GGTGTTAGTGTCCTG[C/T]GGAGGAAGAAATCAA | 9690 |
rs745447409 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173301 | GGATCGTTTGAGCCC[A/T]GGTATTCAAGGCTGC | 9690 |
rs745452249 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235798 | CTGTGTGGAAATTCC[C/T]AAGGGGTTACTAACT | 9690 |
rs745465142 | in-del | -/TTC/TTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242527 | TGTTTTTTTTTTTTT[-/TTC/TTTT]TTTTTTTTTTAAATT | 9690 |
rs745479714 | snp | A/G | 3.68657e-05 | 0.00429319 | intron-variant | UBE3C | GRCh38.p7 | 7:157182080 | GTATAATTTGATTTT[A/G]TAAAAAGCTTCTGTT | 9690 |
rs745485643 | in-del | -/CCCAAAGTTA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174709 | TGCCTGCCTCAGCCT[-/CCCAAAGTTA]CAGACGTGAACCACT | 9690 |
rs745533967 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260950 | TGGCCACTTGTGCTG[C/T]GTGAGCGTCGTAGGT | 9690 |
rs745534245 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141715 | TGACTGTCCTTCTGA[C/T]CTCCATTACTGTAGA | 9690 |
rs745536390 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236654 | AATTGAGGTGAATAC[G/T]AGTCATTTTGGTTGC | 9690 |
rs745569047 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188445 | TGTGGCTCCTAGATT[A/G]GGTCCTTAGCTCTTT | 9690 |
rs745574710 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161582 | TCAACCCCCAAGTAG[C/T]TGGGACTGCAGGCAT | 9690 |
rs745577981 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242860 | AGGAGTTCTAGACCA[G/T]CCTGACCAACATGGT | 9690 |
rs745578055 | snp | C/G | 1.65296e-05 | 0.00287481 | intron-variant | UBE3C | GRCh38.p7 | 7:157201706 | GTTCTGTGTTTTTCT[C/G]CTATTCCTTTTTAGG | 9690 |
rs745590383 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201004 | AAGTGACTTGAGTCC[A/G]TCACTAAATATTTTA | 9690 |
rs745606107 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239633 | ATTGGGGGACTGGTT[A/G]TCAAGAAAACTTGAG | 9690 |
rs745621632 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256785 | GATACACACATGCCA[C/T]GCCGTTTTAGAGAAG | 9690 |
rs745628794 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165787 | TTATATAGTCTTTAG[C/T]TCTCTTTTAATTTCT | 9690 |
rs745655581 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191286 | TGTTTGTTGGTTTTG[C/T]CTTTATTTTTGTTTT | 9690 |
rs745679416 | snp | A/T | 0.000115417 | 0.00759574 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186873 | TACATAACAGAGGAA[A/T]GCCTGAAGAAGCTGG | 9690 |
rs745690343 | snp | C/T | 1.76824e-05 | 0.00297336 | intron-variant | UBE3C | GRCh38.p7 | 7:157178643 | TGGGGAAACTGGTGA[C/T]ATTTTGCCATCCTGT | 9690 |
rs745691713 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204917 | GGGGACATTGGACGA[C/G]GAGGAGGAGTGGTTC | 9690 |
rs745701256 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230278 | GCCAAATACAGCTTT[G/T]AAAAGATCACGTAGA | 9690 |
rs745734804 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253981 | AAATTCGGTGGGAAA[A/G]ACATCCCTGTCACCA | 9690 |
rs745750237 | in-del | -/GCTCTCTCTGCCCCAGGCCTGGGGCTGTTTTCTCTAAGG | 1.658e-05 | 0.00287919 | intron-variant | UBE3C | GRCh38.p7 | 7:157178853 | TTCACAATGGTAAGT[lengthTooLong]AGTAGGCAGGATCAG | 9690 |
rs745753206 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154442 | GTCTAAACATAAACA[C/T]GTCCTCCCCTCTCAT | 9690 |
rs745762352 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249753 | TTTGGGTTGTTCCTA[G/T]GTTTGGGCTAATAAG | 9690 |
rs745770395 | in-del | -/TGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166915 | GCTTTTTCCTGTTGG[-/TGG]TGGTGGTGGTGGTGG | 9690 |
rs745785176 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220377 | AACTTAATTTTTAAA[A/G]TGATCTATTTTGCTT | 9690 |
rs745849593 | snp | A/G | 3.51673e-05 | 0.00419314 | intron-variant | UBE3C | GRCh38.p7 | 7:157216846 | TCACGTGTGTGACGC[A/G]GATATGTTCTTTCTT | 9690 |
rs745865311 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142816 | TATTCTTGTAACAAA[C/T]GTGCATAGGTACCCC | 9690 |
rs745876691 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155625 | CTTTACTATTTCAAA[G/T]AAAGAATAAACTTTG | 9690 |
rs745890312 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232992 | ATCACCAATATCAAA[C/T]TTGGAAGCAATGTCA | 9690 |
rs745923265 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182258 | GTTAATAGAGAGTAG[A/G]TGTTCAAGAAAGAGT | 9690 |
rs745938170 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169631 | TTCGCCTGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 9690 |
rs745948538 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195809 | GACTTTTGAGCACCT[A/C]TGAGTGACGTAAATT | 9690 |
rs746002720 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233855 | TCCACATCGTTGTCA[A/G]CACTTACTTAGTGTT | 9690 |
rs746010456 | snp | C/G | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207400 | TCTTTAATTCAAGGT[C/G]TATGGTACCGTTGCT | 9690 |
rs746043614 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258239 | GGTGTGAGCCACCAC[A/G]CCATGCCCAGCTGGC | 9690 |
rs746055667 | snp | C/T | 4.05474e-05 | 0.00450245 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139248 | TCCGCGGCGGCGCTG[C/T]CCGCACATGGGCTAG | 9690 |
rs746064135 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157540 | GGCAATTTGGAAATA[C/T]TCATTAAAATTCAAA | 9690 |
rs746080784 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223761 | CCTGTCTCTACAAAG[A/C]ATACAAAAGTTAGTT | 9690 |
rs746102111 | snp | A/G | 1.65272e-05 | 0.0028746 | intron-variant | UBE3C | GRCh38.p7 | 7:157225389 | TCTAATAACCTTACA[A/G]CTTTCCTTGTTTGTT | 9690 |
rs746117184 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185563 | TCATTCTTTCTTTGC[C/T]ATGTCTCTTACCTGT | 9690 |
rs746144552 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174374 | TCAGATTGACATGAG[C/T]TTTAAGTGTACTTTG | 9690 |
rs746175265 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216255 | TTTCTCAGAAAACTC[A/G]GAAATACTCTTTCAG | 9690 |
rs746203117 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150615 | GTGAAATACTGTGCA[A/G]CCATTTAAAATGGTC | 9690 |
rs746203285 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250238 | TGTATTGTTTTGAGA[C/T]GGGGTTTCACTCTGT | 9690 |
rs746226528 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182760 | TTGGGGGTTGGGTGC[-/TG]GGGGGGGTATATAGA | 9690 |
rs746239149 | snp | A/G | 1.75644e-05 | 0.00296342 | intron-variant | UBE3C | GRCh38.p7 | 7:157170486 | CACTTGTCCTCGTTT[A/G]CACGTGTTCTGCTTT | 9690 |
rs746313180 | snp | C/T | 1.65919e-05 | 0.00288022 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253987 | GGTGGGAAAGACATC[C/T]CTGTCACCAGCGCCA | 9690 |
rs746320697 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178640 | ACTTGGGGAAACTGG[G/T]GACATTTTGCCATCC | 9690 |
rs746328697 | snp | A/G | 3.31164e-05 | 0.00406904 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170376 | GCTTTTCCCATTGCT[A/G]ATGGCCCCAACCTTA | 9690 |
rs746334672 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140185 | CCACCCCTTCCCATC[A/G]TTTCTGAAATGTTCT | 9690 |
rs746363966 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241368 | AGATACTTGTGGCAT[A/G]TATATGAAGGACTCC | 9690 |
rs746409200 | in-del | -/AT | 1.6473e-05 | 0.00286988 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256977 | TGGAAGGGTTCACTG[-/AT]GAAGAAAAGCGCAAA | 9690 |
rs746428700 | snp | A/C | 1.66518e-05 | 0.00288542 | intron-variant | UBE3C | GRCh38.p7 | 7:157182336 | TTATTTGGGTATGAA[A/C]TACAAGATCTTTTTT | 9690 |
rs746449328 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209366 | TGGGCAGATTGATGT[A/G]ATATATGTTTGCACA | 9690 |
rs746481199 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230034 | CGGCCTCAGCCACCC[A/G]AGTAGCTGGGATTAC | 9690 |
rs746490159 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253730 | GAAACATGGATGGTT[A/G]GTGATCTTAAAGACA | 9690 |
rs746493786 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141935 | TGCACATAATACTCT[C/T]GTGCTGGGTCCTAGA | 9690 |
rs746498801 | in-del | -/GG | 1.66549e-05 | 0.00288568 | intron-variant | UBE3C | GRCh38.p7 | 7:157220657 | GTGTGCTAGAGCACA[-/GG]GGAGTTCTGAACCAG | 9690 |
rs746534009 | snp | G/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181618 | AAAAATTTTGCTAGA[G/T]AATGTTCTAAAACCA | 9690 |
rs746542848 | in-del | -/GCAGGTGG | 1.64749e-05 | 0.00287005 | intron-variant | UBE3C | GRCh38.p7 | 7:157254349 | GTTTCTGAAAATGTT[-/GCAGGTGG]TCATATTTCCAAAGT | 9690 |
rs746558557 | in-del | -/AAAAAAATGAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154026 | AACTTTTTCTGTTTA[-/AAAAAAATGAT]AGGCCGGGCACGGTG | 9690 |
rs746581732 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208972 | CACTAATGTTCAGTT[C/T]GAGTCATCAGCTGTC | 9690 |
rs746583644 | snp | C/T | 1.79961e-05 | 0.00299962 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267801 | AACCAGTGCTTCCTT[C/T]GTCAGCAGCGCCTCC | 9690 |
rs746600702 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231540 | ATGTTGAAACTTGAT[-/C]CCCCAGTGTGCCAGT | 9690 |
rs746603801 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182780 | GGGTATATAGAGTCT[C/T]GCTCTGTCACTAGGC | 9690 |
rs746618098 | snp | G/T | 1.66327e-05 | 0.00288376 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181519 | GTTTTTCCTTTTAGG[G/T]TATTATAGGTCTCTA | 9690 |
rs746620341 | snp | C/T | 3.90312e-05 | 0.00441748 | intron-variant | UBE3C | GRCh38.p7 | 7:157188972 | AATGAATGTGGAGAC[C/T]TTTGTACCCTGACAT | 9690 |
rs746668252 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244199 | CGTGCCATTCATTGC[A/G]CTCCAGCCTGGGCGA | 9690 |
rs746693872 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176447 | GCCCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 9690 |
rs746709723 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159388 | TAAACCAGTTGGTGG[C/T]GGTGAATGGATAAAG | 9690 |
rs746712407 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229809 | TAGAGACAGGGTCTT[A/G]CTAGTGTTGCCCAGG | 9690 |
rs746733047 | snp | G/T | 1.98553e-05 | 0.00315075 | intron-variant | UBE3C | GRCh38.p7 | 7:157223200 | TAAGAATTGTCAGTG[G/T]GAATGCAGGGGAAAG | 9690 |
rs746741744 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213284 | GCTATCTTACTTCAT[A/G]TAACTTACCACACTG | 9690 |
rs746759084 | snp | C/G | 4.94727e-05 | 0.00497332 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220700 | ACAGGTCACTCAGCT[C/G]TATGTGCCAGCATCC | 9690 |
rs746804527 | snp | C/T | 4.94564e-05 | 0.0049725 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184011 | GGAGAGTGAAGAAGC[C/T]GACAAGCCCTCAAGC | 9690 |
rs746805703 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175486 | CTGCCGTGACTTTCT[A/T]GCATTCAGTGTCCGA | 9690 |
rs746915507 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189928 | ACTTCAGCCTCCCGA[A/G]TAGCTGAGATTACGG | 9690 |
rs746915993 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190578 | AGGTGCTGGTGGGCG[G/T]TGCTGCCCAGGGTTT | 9690 |
rs746933592 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203415 | GTTGTGTTTTTTTTG[G/T]TGCATTTCAGCCACT | 9690 |
rs746947468 | snp | A/G | 1.65583e-05 | 0.00287731 | intron-variant | UBE3C | GRCh38.p7 | 7:157169016 | ACTGGATTCTGACCA[A/G]TTGCTCCCTCACTCC | 9690 |
rs746969892 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207752 | TACTTTAGAAGAGCT[A/G]ATAATGTTGTCTCGA | 9690 |
rs746969955 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188990 | TGTACCCTGACATGG[A/G]AAGATTTCCGAGACA | 9690 |
rs747003186 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261509 | ATTTTTCCATGATAA[-/GT]GTTTTTGAAGTTGTT | 9690 |
rs747004745 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153699 | CTCTGCAGTCAGTGG[A/C]CTTTTTAAAAAGTTA | 9690 |
rs747018863 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217417 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGACG | 9690 |
rs747052922 | snp | C/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201751 | AGCCTTTAATGCCAG[C/G]TTTCTGAGACATCTT | 9690 |
rs747081211 | snp | C/G | 1.65318e-05 | 0.002875 | intron-variant | UBE3C | GRCh38.p7 | 7:157225387 | TTTCTAATAACCTTA[C/G]AGCTTTCCTTGTTTG | 9690 |
rs747102879 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252937 | GAAATACAGGTGGGG[G/T]TCTTGCTTTATCTCA | 9690 |
rs747146757 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216260 | CAGAAAACTCAGAAA[-/T]ACTCTTTCAGGAAAA | 9690 |
rs747148978 | snp | C/G | 1.7079e-05 | 0.00292219 | intron-variant | UBE3C | GRCh38.p7 | 7:157175080 | ATAATGTATTGATCA[C/G]CTTGTCTAGGGGAAC | 9690 |
rs747153281 | snp | A/G | 1.68949e-05 | 0.0029064 | intron-variant | UBE3C | GRCh38.p7 | 7:157223359 | GAGTAAAGGTATGCA[A/G]TTTGGCTTCTTTATT | 9690 |
rs747158169 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241161 | CACGCAGAGTGCTCT[C/G]AGGATCACAGAGCGC | 9690 |
rs747174953 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162686 | CTGGGACTACGGGCA[C/T]ATACTGCTGCACCCA | 9690 |
rs747180157 | snp | A/G | 8.24531e-05 | 0.00642026 | intron-variant | UBE3C | GRCh38.p7 | 7:157257058 | AGGTACACAACTTTC[A/G]TGACATTTGCTTTAA | 9690 |
rs747206847 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183508 | GTCCCTCCCACAGAC[A/G]GCCCCTTGGAAGTTG | 9690 |
rs747238586 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221865 | TTTTTTGTTGTGTTT[G/T]CTTGGTTGTTTTTTG | 9690 |
rs747241821 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151818 | TGTCACCATGACAAC[C/T]GTGGAGCAGGAGGTA | 9690 |
rs747242967 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195595 | TGTTACTGTATGCCT[G/T]TCACACCATCATACA | 9690 |
rs747248709 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145152 | AGGCTGAGGCAGGAG[-/A]ATTACTTGAGCCCTG | 9690 |
rs747248755 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194206 | ATACATTATACAGGT[G/T]GTTTTCAGTTAAGTG | 9690 |
rs747253586 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203694 | TTTATGATAGGGTAG[C/T]TTTACAAATCTTATT | 9690 |
rs747296561 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144227 | CTGGATCCCGGGAGT[C/T]CAAGGCTGCAGTGAG | 9690 |
rs747323789 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198070 | GGATCTCTCCTCTTT[C/T]AACAAACTCCAGAAA | 9690 |
rs747332976 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | UBE3C | GRCh38.p7 | 7:157248594 | AGGTGAGGGGTCAGG[A/G]GGAGGATTCACATAC | 9690 |
rs747338487 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197246 | CAATGCTGCATCAAG[A/C]AACTTTAGTGCAAAT | 9690 |
rs747344925 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244857 | CCATATACCTATTGC[A/T]ATTTTTTTCATGACA | 9690 |
rs747369251 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260192 | GGGGGGTGGGGGTGG[A/G]AAGTAACATTCAGAA | 9690 |
rs747379689 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160264 | ATTTTTAGTAGAGAC[A/G]GGGTTCCACCATGTA | 9690 |
rs747394082 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260909 | GAGAGCCTTCTCCAC[C/T]TCCGTGATGCCTCCG | 9690 |
rs747441001 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225961 | TCTCCAAAAAAAAGT[A/G]TAGCAAGTCAGATTT | 9690 |
rs747459423 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226867 | TTTGTCTTGCCTAGC[A/G]GATTGTGTTTTCAGA | 9690 |
rs747467467 | in-del | -/AA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182390 | ATTGGCAGATGAGTC[-/AA]GAGAAGGCCATGCAG | 9690 |
rs747473700 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182248 | ATGCACTGTTGTTAA[C/T]AGAGAGTAGATGTTC | 9690 |
rs747477825 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250055 | GGCCCAAGTATTTCA[C/T]TCAGATAAGGGATAC | 9690 |
rs747482007 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150449 | TCTACATTTAGAAAC[A/G]TAAAAATTTATTCTA | 9690 |
rs747500001 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188329 | AGTAAGGAACCCATC[C/G]GTTGAAATGGCCTTG | 9690 |
rs747507733 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149302 | CTCAGGTGATCCACC[C/T]ACCTCAGCCTCCCAA | 9690 |
rs747524507 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138336 | TTGATGCTGTATCTA[C/T]AGATGCATATGTGTG | 9690 |
rs747534210 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177082 | GTCACATAGTAGTTA[C/T]ATATTTCACTTTAGA | 9690 |
rs747597881 | snp | A/T | 8.2659e-05 | 0.00642827 | intron-variant | UBE3C | GRCh38.p7 | 7:157207390 | TTTCTTCTTTTCTTT[A/T]ATTCAAGGTCTATGG | 9690 |
rs747609179 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189724 | TTTTCCTTTACTTGG[G/T]CTTCTCAGTTTCCTT | 9690 |
rs747649432 | snp | A/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267693 | GAGTTCTATGACGAG[A/T]CACTTTTGCGAAGTA | 9690 |
rs747652609 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227698 | AGTGAGACTTCATCT[C/G]AGAAAAAAAAAAGAA | 9690 |
rs747662681 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190392 | CTGCAGCCTGAAACT[G/T]CAGTGTCCTGCATGG | 9690 |
rs747665782 | in-del | -/TT | 1.65141e-05 | 0.00287346 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182321 | AACTGTTGGCGAAAA[-/TT]ATTTGGGTATGAAAT | 9690 |
rs747677251 | snp | C/G | 6.59272e-05 | 0.00574101 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178802 | CAAGATGCTAGCTAT[C/G]TGGTGTCAGTGATTG | 9690 |
rs747704668 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158589 | ATTCCTTTGTCTAAT[A/G]ATTTAGCTCATTGTC | 9690 |
rs747710729 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153393 | GAACCAACTGTCTGT[A/G]ACTTAGCTGTTCATC | 9690 |
rs747738966 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180134 | GCTTCTAGCATCTTC[G/T]GTGGTACAGCAGTTG | 9690 |
rs747752988 | in-del | -/A | 2.75562e-05 | 0.00371178 | intron-variant | UBE3C | GRCh38.p7 | 7:157217006 | TTAATATTTATCATT[-/A]AAAAATACATTCAGC | 9690 |
rs747786897 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190987 | GCTTGGCTCTTTTAC[C/T]CCATTGATGGATCTA | 9690 |
rs747794484 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169973 | ACAGGTGTGAGCCAT[C/G]GTGCCCTGCCTAGCT | 9690 |
rs747799613 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141185 | GTAGGAACTGGCAGC[A/G]GCTGGGGCATGGGTG | 9690 |
rs747874893 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181117 | CCTTCCTGATGCAAG[A/C]AAACTAGTTAAATAG | 9690 |
rs747917737 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145221 | ATTCCAGCCTGGGTG[A/G]CAGAGCATGACTCTG | 9690 |
rs747936202 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246167 | TCTCAAGGGGTGTCT[A/G]AGCATGCCCTGTTGG | 9690 |
rs747936286 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258172 | GGCTGGCCTCCAACT[C/T]CTGGGCCCAAGAAAT | 9690 |
rs747967467 | snp | A/G | 3.29853e-05 | 0.00406098 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207726 | CAAAGACAATCATCA[A/G]TGATGCCTTTTACTT | 9690 |
rs747975785 | snp | C/T | 1.65468e-05 | 0.00287631 | intron-variant | UBE3C | GRCh38.p7 | 7:157163886 | CAGTTTTGTAATACT[C/T]TGTAGATAAGCATTT | 9690 |
rs748000809 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148398 | GTGAGCCACCATGCT[G/T]GGCCTCAATTACTCT | 9690 |
rs748038606 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250756 | TACTGTCATTAGGAA[-/GT]GTACTCGACATCCAG | 9690 |
rs748069637 | snp | A/C | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181606 | AGTTCCTATAGCAAA[A/C]ATTTTGCTAGAGAAT | 9690 |
rs748073872 | snp | A/C | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231224 | ACCAGGGGTTCTTTA[A/C]GACTACTAATGAAGG | 9690 |
rs748084785 | snp | C/G | 1.64914e-05 | 0.00287149 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267791 | CCCTACAGAGAACCA[C/G]TGCTTCCTTCGTCAG | 9690 |
rs748107215 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262906 | TGGGACATTGCTCTA[A/G]TTTGATTCACATTTG | 9690 |
rs748111286 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169623 | TCAAATGATTCGCCT[G/T]CCTTGGCCTCCCAAA | 9690 |
rs748129073 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238143 | ATGTAACTTTATGAA[A/G]TAAAAGCCAAATGAA | 9690 |
rs748146031 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163020 | GAAAAAAAATTTTCA[A/T]CAAAGAAATTGATTT | 9690 |
rs748151685 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192042 | GCACATAGTGATCTT[-/A]AAATTAAATGTATTT | 9690 |
rs748195531 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203888 | AAATGCATTCAAGAC[A/T]CCCAGCTTACTGAGG | 9690 |
rs748199124 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149072 | TTCTTTTTTTGTTTT[C/T]TGAGATAGAGTTTTG | 9690 |
rs748225243 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | UBE3C | GRCh38.p7 | 7:157254361 | GTTGCAGGTGGTCAT[A/G]TTTCCAAAGTAATTT | 9690 |
rs748229449 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266808 | GTGGTGTGATCATAC[C/T]TCACTAACCTCGACC | 9690 |
rs748251254 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174965 | GCTCTCTGTTTGTCA[A/G]GCAGTTGGATGGATC | 9690 |
rs748266956 | snp | A/G | 1.66899e-05 | 0.00288871 | intron-variant | UBE3C | GRCh38.p7 | 7:157254221 | TTTACCTCAAATGTT[A/G]TTATTTGAACTTTTT | 9690 |
rs748269472 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176859 | TCTTTTTGATGAGAA[A/G]TGGAATTTTAACAAA | 9690 |
rs748302564 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166682 | GAGGCGGAGGTTGTG[A/G]TGAGCTGAGATCACG | 9690 |
rs748318743 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177716 | GCTGGGTCCTCACCC[C/T]CTGTCTCTCCTGGGC | 9690 |
rs748327221 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142023 | CCCACAGCATCTGAA[A/G]GTATCCAGGTTTCCA | 9690 |
rs748339231 | snp | A/G | 1.70927e-05 | 0.00292336 | intron-variant | UBE3C | GRCh38.p7 | 7:157174875 | AATTAGCAAACTATT[A/G]AATTTTCATTGAGAG | 9690 |
rs748355910 | snp | A/C | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138212 | TACATTTTCAACTTA[A/C]AATATTTTCATCTTA | 9690 |
rs748359691 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188279 | AAAAGAGTGATTTCT[G/T]TTGGCTAAGAAAGCA | 9690 |
rs748375354 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157976 | CAGATATATATAGAT[-/AT]ATATATATATAGAGA | 9690 |
rs748402430 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266341 | AAATAAAAATAATAG[A/G]GTAACTGGGTTGCTT | 9690 |
rs748427123 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183906 | GGAAGGGCTGCTGGT[A/G]TATTTGCGGGTGCTG | 9690 |
rs748443654 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254733 | ACTCTTTTGTAGGGG[G/T]AATGTACATGGTTCA | 9690 |
rs748444914 | snp | A/G | 1.72478e-05 | 0.00293659 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182123 | GCAACAAGTTTTTAC[A/G]GCCTTCACAGAGGAG | 9690 |
rs748445281 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166901 | CATCTGGTGAAAGTC[A/G]CTTTTTCCTGTTGGT | 9690 |
rs748472268 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154606 | ACCACTTTCCTATCA[A/G]TGGATACATATAAAT | 9690 |
rs748473875 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234014 | CAAGTCCATTGCCTA[A/T]TTTTTTATTGGATTG | 9690 |
rs748495412 | snp | A/C/T | 0.000215803 | 0.0103854 | intron-variant | UBE3C | GRCh38.p7 | 7:157207371 | TTTTAAAGTGACTGG[A/C/T]TTTTTTCTTCTTTTC | 9690 |
rs748532334 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157921 | GGAGGCGGAGGTTGC[A/G]GTGAGCCAAGATCGT | 9690 |
rs748536561 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209573 | TGTTAACGGTAGCAT[A/G]TTTGTTTTCCTTTCA | 9690 |
rs748569408 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176599 | TTCTTTAACAACAAG[-/A]AAAACACTCCTCCTC | 9690 |
rs748583478 | snp | G/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201723 | TATTCCTTTTTAGGC[G/T]TCTCTACAGTTTAGC | 9690 |
rs748595990 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198011 | ATGGTCCTCCATATC[C/T]CAATTCACTTGGCCA | 9690 |
rs748637195 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260001 | AAATAGGTCAATCAT[C/T]GACGCCGTTATGTTC | 9690 |
rs748639288 | in-del | -/A/AA/AAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230694 | GGCAGACCCCGTCTC[-/A/AA/AAC]AAAAAAAAAAAAAAA | 9690 |
rs748651672 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235392 | ATAATTTTACCTGCA[C/T]GAATTAAATCTTAAG | 9690 |
rs748671348 | snp | A/G | 1.65348e-05 | 0.00287526 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223318 | TGTCCTGACAGAGTT[A/G]CCTTTTGTGGTTCCA | 9690 |
rs748714278 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147811 | TATGTGATTTTCCTT[C/T]TGCAGCTTGTGGATA | 9690 |
rs748720860 | snp | C/T | 1.6617e-05 | 0.00288239 | intron-variant | UBE3C | GRCh38.p7 | 7:157220665 | GAGCACAGGGGAGTT[C/T]TGAACCAGGATTGCC | 9690 |
rs748770099 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174115 | CGTGTATAATCCCAG[C/T]GCTTTGGGAGGCTGA | 9690 |
rs748779110 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236772 | AGTCTCACTCTGTTG[A/C]CCAGGCTGGAGTGCA | 9690 |
rs748786350 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237848 | CCCAGGAGTTCAAGA[C/G]CATCCTAGGCATACA | 9690 |
rs748812059 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240805 | AGGGGCTTAGTTACC[A/G]GTAATGCCACTTGGA | 9690 |
rs748823122 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162677 | CCTGAGTAGCTGGGA[C/T]TACGGGCACATACTG | 9690 |
rs748832775 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227075 | ACAGCTTGGGATGGA[A/G]TTGTTTATTTGGTGT | 9690 |
rs748835588 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201252 | CCCCTTGAACCCAGG[A/T]GGTGGAGGTTGCAGT | 9690 |
rs748884121 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189592 | CATGTAGATGAGGCC[C/T]GCGGTGCCCACTCAG | 9690 |
rs748884815 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151022 | GGCAGCTGGCCTCCC[A/G]CTAAGCTGCTGAGCA | 9690 |
rs748928101 | snp | G/T | 1.68972e-05 | 0.0029066 | intron-variant | UBE3C | GRCh38.p7 | 7:157216862 | GATATGTTCTTTCTT[G/T]TCAGGTTATCACCAA | 9690 |
rs748931373 | snp | C/T | 0.000346744 | 0.0131625 | intron-variant | UBE3C | GRCh38.p7 | 7:157169036 | TCCCTCACTCCTCCT[C/T]TTATTGTTTAGGAAG | 9690 |
rs748958394 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248397 | CATGCTGGTGGAGCT[A/G]CCCTTTGCAGGCTTC | 9690 |
rs748982306 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205849 | TCCTTTTCTCAAAGC[A/G]GTTGATGATGGCAGT | 9690 |
rs748982331 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206013 | CTCCTGGTTACATCT[C/T]ATCTAATATATACCT | 9690 |
rs748984912 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249856 | TGCTTCAAATACACT[-/C]TGTGCATCCATAATC | 9690 |
rs748986517 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253111 | AAATTATGATTACAT[A/G]TTTATATTGTATTTT | 9690 |
rs749007844 | snp | A/G | 0.000164753 | 0.00907465 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182208 | GCAGATGCGCAGACC[A/G]TTTTCCCTTACGAGC | 9690 |
rs749016199 | in-del | -/TGCGCGGCCGGGGCTCGGGGCT | 4.23684e-05 | 0.00460243 | intron-variant | UBE3C | GRCh38.p7 | 7:157139378 | CCTCGGCTCGGGGCC[-/TGCGCGGCCGGGGCTCGGGGCT]GGGACTCGGGGCTGG | 9690 |
rs749029350 | in-del | -/C | 1.64954e-05 | 0.00287183 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181637 | GTTCTAAAACCATTG[-/C]ACTTTACTTACAACT | 9690 |
rs749075687 | snp | C/T | 1.67961e-05 | 0.00289789 | intron-variant | UBE3C | GRCh38.p7 | 7:157231029 | GGCTAGTTGATGTTA[C/T]TGCTTGCTTGTAACA | 9690 |
rs749081133 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187561 | AATTTTTTGTTTTTG[-/TG]TGTGTGTGTGTGTTT | 9690 |
rs749081308 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193802 | TTGAGATGATTACAA[A/G]TTTAAGATGACTGCA | 9690 |
rs749081638 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221719 | TGCACTCCAGCCTGG[A/G]TGACAGTATAAGACT | 9690 |
rs749087255 | snp | A/T | 2.25619e-05 | 0.00335864 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139300 | GAAGGCGACTTCAAG[A/T]CGCGGCCCAAGGTGT | 9690 |
rs749099865 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244727 | GACTGCACTCACTTA[C/T]ATTAAAAGGCTTCTA | 9690 |
rs749108114 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201637 | TCTTCAGTGTATCGC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs749152032 | snp | A/G | 1.75566e-05 | 0.00296277 | intron-variant | UBE3C | GRCh38.p7 | 7:157170482 | TTTTCACTTGTCCTC[A/G]TTTACACGTGTTCTG | 9690 |
rs749155877 | snp | C/T | 0.000148247 | 0.00860822 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256988 | ACTGATGAAGAAAAG[C/T]GCAAACTGCTGAAGT | 9690 |
rs749173204 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152358 | ACTTAGGTTTTAGAG[A/G]TGCGTGGGGGGCAGT | 9690 |
rs749177317 | snp | G/T | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178781 | AATACTTACTTGCCT[G/T]TTTTACAAGATGCTA | 9690 |
rs749178578 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229220 | AAAGATAAAGGACAT[G/T]TCACTTACTTCCCCA | 9690 |
rs749186737 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | UBE3C | GRCh38.p7 | 7:157267541 | AAAACTCATGTAATG[C/T]CATGCTTGTTACAGT | 9690 |
rs749196473 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267678 | CTGCTGAAGCTCCCC[A/G]AGTTCTATGACGAGA | 9690 |
rs749207685 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183683 | TCTTTCAAGAAATTA[C/T]AAGAGTTGTAGGTGC | 9690 |
rs749227725 | snp | A/C | 1.66012e-05 | 0.00288103 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186910 | AGCAGCAGACCAACA[A/C]CCTGCTCAACCTGGT | 9690 |
rs749243446 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222689 | CAGCCTGGGATTACA[A/G]GCATAAGCTGCCATC | 9690 |
rs749264110 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145083 | GAGACCAGCCTGGCC[A/G]ACGTGGTGAAACCCC | 9690 |
rs749284887 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223874 | GCAGTGAGCCAAGAT[A/C]GTGCCAGTACACTCC | 9690 |
rs749300604 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226937 | CCTAATCTAACTAAT[C/T]GTCTAATTGAGAGAT | 9690 |
rs749332335 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259179 | CAGGCCCCACTCAGA[C/T]CTGAGTCAGCGCTCA | 9690 |
rs749346378 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158842 | ATGACAACATAGACT[C/T]CAAGTGTGTTGAATG | 9690 |
rs749425846 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259944 | TTGGGACCCAGTAGA[A/G]AGGTGGAAAGAAGTG | 9690 |
rs749438861 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247896 | TGTGGGCACGGCCTT[A/G]TTTGGAAATAGGGTC | 9690 |
rs749448386 | in-del | -/ACATGGCG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263478 | CGACCAGCCTGGCCA[-/ACATGGCG]AAACCCCATCTCTAC | 9690 |
rs749472162 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248678 | GCGTTTGACTTCCGC[A/G]CATTTTAGTTAGAAT | 9690 |
rs749484782 | snp | A/T | 9.93953e-05 | 0.00704896 | splice-acceptor-variant | UBE3C | GRCh38.p7 | 7:157207701 | TGGATTGTGTTTTTT[A/T]GTTGTAGGTCAAAGA | 9690 |
rs749484873 | snp | A/G | 1.69755e-05 | 0.00291332 | intron-variant | UBE3C | GRCh38.p7 | 7:157182356 | AGATCTTTTTTACCT[A/G]AACACACATATGGGT | 9690 |
rs749487911 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147603 | AGTTGAAAAGGAGTG[A/G]TGAGAACTTGCCTTG | 9690 |
rs749529020 | snp | C/G | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231189 | TTTAAATGAACTACT[C/G]AAGTCAGGATTTAAC | 9690 |
rs749532979 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238883 | AGAGAAGTGGGATTT[C/T]AGGTGCCAAATAAAG | 9690 |
rs749568744 | in-del | -/GGCATGAGC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170097 | AGTGCTGGGATTAAA[-/GGCATGAGC]CACCATGCCTGGTTT | 9690 |
rs749577117 | snp | A/G | 4.12499e-05 | 0.00454128 | intron-variant | UBE3C | GRCh38.p7 | 7:157139375 | CGCCCTCGGCTCGGG[A/G]CCTGCGCGGCCGGGG | 9690 |
rs749587397 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218307 | AAAATTAGCCAGGCA[C/T]GGTGGTGTGCGCCTA | 9690 |
rs749592021 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165028 | GTTTAGCAACACCCA[C/T]GGCCTCTACCCACTA | 9690 |
rs749601478 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211634 | ACTAGGCATAAATGG[G/T]TTAACAAGTGGTAAC | 9690 |
rs749639266 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141114 | GGGAGTGTGGCACTG[C/G]TAACCCTGAGCCGAG | 9690 |
rs749643423 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241409 | TGGGCGAAGGATCCA[A/G]TTGGACATCTCTCCA | 9690 |
rs749651281 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252179 | GTTTTCTCTGATCAG[A/G]CAAGGTAATTGGGAG | 9690 |
rs749653547 | in-del | -/TT | 1.64773e-05 | 0.00287026 | intron-variant | UBE3C | GRCh38.p7 | 7:157267547 | CATGTAATGCCATGC[-/TT]GTTACAGTGACATCT | 9690 |
rs749671479 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219074 | GGATTTTTGCAAACT[A/G]GAATCAGCCTGTTGC | 9690 |
rs749718372 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159044 | ACTCCTGTGAAAGGC[A/G]GAGACTTAATTCTCT | 9690 |
rs749720159 | in-del | -/GGCATGAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170096 | AGTGCTGGGATTAAA[-/GGCATGAG]GGCATGAGCCACCAT | 9690 |
rs749725330 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208882 | TTGCTCATTAAAGGA[G/T]TGAGAGCAGAAGAAA | 9690 |
rs749728357 | snp | A/G | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269565 | CCCAGGCCGGCGGCC[A/G]GTGTGCTCCTATCCG | 9690 |
rs749741234 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242375 | CAAATTTCTCAAGAG[A/G]TGGCTCGACAGATTT | 9690 |
rs749768573 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233945 | TTCCCTGGTGACTAA[C/T]AATGTTGACCATCTT | 9690 |
rs749773273 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181339 | GACAGTTGTTGGTAC[A/G]TGAGGTTTGTATACC | 9690 |
rs749791071 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201494 | GGGAGGGAGGGCGGG[A/C]TTTCCTAGCTTGGTA | 9690 |
rs749799785 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196013 | CTATGGATTTCAAGA[C/T]GAGGCGATAAGCCCA | 9690 |
rs749808363 | snp | A/T | 1.71903e-05 | 0.00293169 | intron-variant | UBE3C | GRCh38.p7 | 7:157220814 | TTACTGAGGTATGAA[A/T]TACATGCTGTCAAAT | 9690 |
rs749871629 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156211 | AAGTGAGAAAATATT[A/G]TAAGTACATGGGTGA | 9690 |
rs749875768 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256853 | TCTGGACCAATCCCT[C/G]TGGGTCCTGAAGGGT | 9690 |
rs749925667 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268361 | CATGCTTGTTTTCAG[C/T]ATACCGTGGCCTGCC | 9690 |
rs749926772 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183528 | CTTGGAAGTTGGTGC[A/G]TGGGGCTGAAAGTTC | 9690 |
rs749950272 | in-del | -/ATC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212513 | CAAGATTTTCTTATG[-/ATC]ATCATTGCCATGAAC | 9690 |
rs749958486 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207447 | GGTTCTCCTATGTCT[G/T]TTGAAGATTCTAGTC | 9690 |
rs749970532 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233420 | AGTAGCTGGGACCAC[C/T]GTTGCTTGCTACCAC | 9690 |
rs749972114 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222564 | AGCTGGGACTATAGG[C/T]GCGTGCCACCATGCC | 9690 |
rs749998287 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | UBE3C | GRCh38.p7 | 7:157201838 | ACTTATAAATTGAGC[C/T]CAAGGGCACAGGAAG | 9690 |
rs750013703 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257853 | TGCACACAGTGGTAT[A/G]TATATTATAGAATAA | 9690 |
rs750028071 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184158 | TTGCAGAGAAGCCCC[A/G]TCAGCCCCACTACCA | 9690 |
rs750040639 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142564 | GAGAAGGCATTCCAG[A/G]TTCGTGGAGCGGGGT | 9690 |
rs750059578 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211865 | GTGAAGGAGACATGC[A/G]TTCAGCTAATGACAG | 9690 |
rs750065923 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162603 | GGAGAGTGGTAGCTC[-/A]ATCCTGGCTCACTGC | 9690 |
rs750068479 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223272 | GTTTGGAGTCCCCGC[C/T]GCTGTCTGTGTCTGA | 9690 |
rs750084253 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146035 | TCTAGTAGTTTTATA[A/G]TTTTGTATTTTACAT | 9690 |
rs750097763 | snp | A/G | 3.32519e-05 | 0.00407736 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178698 | TTTACAGGTTGCTGC[A/G]AAACTGTAATGATGA | 9690 |
rs750124428 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216202 | TGACAGTGATATCTG[G/T]GGTGCTGCTTTTTTC | 9690 |
rs750139222 | snp | A/G | 0.000115935 | 0.00761277 | intron-variant | UBE3C | GRCh38.p7 | 7:157225362 | TTGGTAGGTTGTAAG[A/G]GGTCTTTTGTTTCTA | 9690 |
rs750154293 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212850 | GCAACCTCCACCCCC[C/G]AGGCTCAAGTGATTC | 9690 |
rs750159597 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210686 | TGAGTTGAAGAATTC[A/C/G]AGGTAGAATCAACCA | 9690 |
rs750173337 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226477 | GAGGGGATTAAAATG[A/G]AAGTTTAGGCTGGAT | 9690 |
rs750185680 | snp | A/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138116 | GATATAAGACACATG[A/T]TTATGTATAGGTGGT | 9690 |
rs750187524 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249308 | GCTGTGGACACTTCA[C/G]ATCGATAGAGTCTTT | 9690 |
rs750204249 | snp | A/G | 1.65323e-05 | 0.00287505 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220757 | GGGGAGGATAGGCCC[A/G]CTGCAGTCCACCCTG | 9690 |
rs750230485 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150075 | GGGTTGGTTATAACA[G/T]ATTTATCAAGAGTCT | 9690 |
rs750257238 | snp | A/G | 1.78618e-05 | 0.00298841 | intron-variant | UBE3C | GRCh38.p7 | 7:157253930 | CTTTGAGGATTTTGA[A/G]ATCCTTACGTTTTGT | 9690 |
rs750264465 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177601 | CGCTCCTCCTGCACT[C/T]GTACACCCCTCGAGA | 9690 |
rs750285454 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157139730 | CACCCAAGGTGAACT[G/T]ACCCTTTCTGGGTGT | 9690 |
rs750306021 | snp | A/G | 3.34213e-05 | 0.00408773 | intron-variant | UBE3C | GRCh38.p7 | 7:157220642 | TGATCAGGTCAAAGT[A/G]TGTGCTAGAGCACAG | 9690 |
rs750307937 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166776 | AATTATTTGAGATTT[C/T]CAAAATTTCTATTTG | 9690 |
rs750316821 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240968 | ATCTTGAATTAAGGG[G/T]CAGTGACTGAACCCG | 9690 |
rs750317882 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178211 | ATAGTAAGAAGGGAA[A/G]CCTCAGTCAAAATGA | 9690 |
rs750340355 | in-del | -/CTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180154 | TACAGCAGTTGTTTA[-/CTTT]CTAACAGTCGATAAA | 9690 |
rs750384077 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167665 | GCCTCTGCCTCCTGG[C/T]AGCTGGGACTATAGG | 9690 |
rs750389461 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147578 | GTCTTACTGCATTAG[A/G]TAGGATTATAGTTGA | 9690 |
rs750432552 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248544 | GGAGCTTGGGCTGAA[C/T]TTCACTGTGGTGAAC | 9690 |
rs750438815 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182287 | GTGGTGGAGCACCCT[C/G]GCTTTTCTATTTCGT | 9690 |
rs750446262 | snp | A/G | 1.66957e-05 | 0.00288922 | intron-variant | UBE3C | GRCh38.p7 | 7:157169162 | ATTAGTAGGGCATGG[A/G]AGAGCTTATTTTAAA | 9690 |
rs750479141 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253095 | AAAATACACTCTTTA[C/T]AAATTATGATTACAT | 9690 |
rs750506263 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151345 | CATAAATAACAACAC[-/AG]TGAGTTAAAAAGCAA | 9690 |
rs750513172 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141623 | ATTATAATCTTATGG[G/T]ACCACGGTGTATATG | 9690 |
rs750535497 | snp | G/T | 3.29897e-05 | 0.00406125 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181579 | AAGTATTGAATATTC[G/T]GATTTATCTCGAGTT | 9690 |
rs750550061 | snp | C/T | 3.58635e-05 | 0.00423444 | intron-variant | UBE3C | GRCh38.p7 | 7:157139369 | GCGGGGCGCCCTCGG[C/T]TCGGGGCCTGCGCGG | 9690 |
rs750553494 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229934 | TATTTATTTTTTTTT[A/T]TTTTGAGACTGTCAC | 9690 |
rs750600407 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234513 | GATGGGAGTAGAACC[A/G]CAGCCTTGTTAAGCA | 9690 |
rs750605003 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170807 | AATACCACATCATGA[C/T]TACTTGCAAACTCTA | 9690 |
rs750624764 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158688 | TCACTAGAGACTGAT[A/G]AGCCCACTGATACTC | 9690 |
rs750625416 | snp | C/T | 3.3222e-05 | 0.00407553 | intron-variant | UBE3C | GRCh38.p7 | 7:157178860 | ATGGTAAGTAGTAGG[C/T]AGGATCAGAACTGTG | 9690 |
rs750650760 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209341 | CTAATGCATCGTTGA[A/G]TTTATAATTTGGGCA | 9690 |
rs750666435 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171298 | ATGCCTGGCTAATTT[C/T]TGTATTTTTAGTAGA | 9690 |
rs750683045 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237258 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 9690 |
rs750685731 | snp | C/T | 8.24029e-05 | 0.00641831 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267674 | GAACCTGCTGAAGCT[C/T]CCCGAGTTCTATGAC | 9690 |
rs750714495 | snp | A/C | 2.21673e-05 | 0.00332914 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186981 | GCCTCCGTCTGCCAC[A/C]CGCTGATGGTGCAGC | 9690 |
rs750730070 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175060 | ATTGTAAGTCAGTAA[C/T]GTATATAATGTATTG | 9690 |
rs750743119 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237796 | CATACCTGTAGTCCC[A/G]GCACTTTGGGAGGCC | 9690 |
rs750748274 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249029 | TATCCTTTTTAAAAA[-/AG]AAAAAAGAAAGGTCT | 9690 |
rs750749749 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247479 | GGTGGATCACCTGAG[C/T]TCAGGAGTTTGAGAA | 9690 |
rs750754742 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201884 | AAATGTTGCCAGAAC[C/G]TGTTTTTAAGTCCTG | 9690 |
rs750766583 | snp | C/T | 3.33167e-05 | 0.00408133 | intron-variant | UBE3C | GRCh38.p7 | 7:157254171 | TGACTTTCTGGGACA[C/T]GCTTGTCACAGGAAA | 9690 |
rs750794140 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162440 | CCTCATGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 9690 |
rs750815935 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187393 | GGGGTTTTTTTTTTT[-/C]TTCTTCTTCTTCAGA | 9690 |
rs750840370 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190092 | GGCGTGAGCCACTGC[G/T]CCCTGCTTAGTTTTT | 9690 |
rs750846760 | snp | A/G | 1.66969e-05 | 0.00288932 | intron-variant | UBE3C | GRCh38.p7 | 7:157183854 | GTTTAACTAAAATAC[A/G]TTTTAACTGATTGTT | 9690 |
rs750889187 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202572 | TGAGGCAGGAGAATC[A/G]CTTAAACCTGGAAGG | 9690 |
rs750913194 | in-del | -/ATTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254393 | ATTTTATTTTAATTA[-/ATTT]ATTTATTTATTTTTT | 9690 |
rs750914438 | snp | C/T | 3.3012e-05 | 0.00406262 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207847 | GAGAAGAATATATTA[C/T]AGCATTTCAGAGTAT | 9690 |
rs750920844 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152041 | TAGGATTCTTAGGAC[A/T]ATTTACATATTAACA | 9690 |
rs750933879 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228361 | ACCGTCACATTCCCT[C/T]ATGGGATTGCTGTAA | 9690 |
rs750940755 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207118 | AGGGCCTTAGTCTGG[A/G]AACGACTGGCTTACT | 9690 |
rs750964207 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252516 | CTTTAAAATGTGAAA[C/T]GTTAAAAGAAGCAGA | 9690 |
rs750969128 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264908 | TTAGCTGTATCTTGT[C/G]TTCAGTTTTCTAGGC | 9690 |
rs750984490 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257254 | CACAATAACCTAGTC[-/AT]ATGATAGTTACACAT | 9690 |
rs751009326 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190861 | AAAGGCATATCTTGC[A/G]TTTTCTTGATCCCAT | 9690 |
rs751009444 | snp | G/T | 1.67206e-05 | 0.00289137 | intron-variant | UBE3C | GRCh38.p7 | 7:157207678 | TGGAAAAAGAAACAA[G/T]AGAAAACTGGATTGT | 9690 |
rs751033800 | snp | G/T | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231270 | CCCGGCTGCTCAGAT[G/T]CTTGTGGGAGATTCT | 9690 |
rs751045662 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250199 | TTCTGTCTACTTTAG[C/T]ATATGGGGCTTTGTT | 9690 |
rs751049102 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247693 | CAAGACTCCGTCTCC[-/A]AAAAAAAAAAGAGCA | 9690 |
rs751063573 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191890 | GAAGTAAATTTTGTC[G/T]ATAATTTCATAGCTG | 9690 |
rs751083746 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205630 | GGCAATGAGGTAGGA[C/T]AATTGTGCTTTGTCC | 9690 |
rs751101997 | snp | A/C | 5.28527e-05 | 0.00514039 | intron-variant | UBE3C | GRCh38.p7 | 7:157223399 | TATCATATTAGTGTT[A/C]AGAAATTAACACACA | 9690 |
rs751129660 | snp | C/G/T | 0.000116418 | 0.00762868 | intron-variant | UBE3C | GRCh38.p7 | 7:157201696 | TTGCTTTACTGTTCT[C/G/T]TGTTTTTCTCCTATT | 9690 |
rs751134948 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267022 | CTGGGACTACAGGTG[C/T]GAGCTATGCGCCTGG | 9690 |
rs751144778 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180548 | TGTTTCAAAAACTAG[C/T]CCATGCAGATGGATT | 9690 |
rs751166488 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230880 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 9690 |
rs751217516 | in-del | -/TTAAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150654 | TATTAATGTCTGTCA[-/TTAAT]TTATTAACATACTTG | 9690 |
rs751217940 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256759 | TGGAAGTGCACAGCA[C/T]GTACACAGGTGATAC | 9690 |
rs751217951 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156032 | TTGAAACCAAAAACT[A/T]GTTAATCAATAGGAA | 9690 |
rs751222439 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221456 | AAAAAAAAAAAATTC[C/T]ATGGGCCAGGCGTGG | 9690 |
rs751226917 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143826 | CAGAATGGTGGCTTC[A/G]AACACAGGTCCTTAA | 9690 |
rs751227200 | snp | C/T | 6.7473e-05 | 0.00580792 | intron-variant | UBE3C | GRCh38.p7 | 7:157254326 | GTATGTTATCACTGC[C/T]AGTTATTGTTTCTGA | 9690 |
rs751256310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231989 | GGAAGTCCAAACTCA[A/G]GGTGTCAGCAGCAGC | 9690 |
rs751275908 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205081 | CAGTAAGTTGCAGAC[-/T]TTATTTGCACATAAG | 9690 |
rs751306999 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147455 | ATTTCCTGCACAGAT[A/G]ATCATTTCATTTGCA | 9690 |
rs751326831 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261753 | CTGCTAAAGCTAATT[A/G]AAGTTTAATATGTTT | 9690 |
rs751332382 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248523 | GAGCTACGAAGACGA[C/T]GTGGAGGAGCTTGGG | 9690 |
rs751334459 | snp | C/T | 1.81355e-05 | 0.00301122 | intron-variant | UBE3C | GRCh38.p7 | 7:157216838 | TGCCGAGCTCACGTG[C/T]GTGACGCGGATATGT | 9690 |
rs751337312 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159746 | GTGGCACATGGTAAT[C/G]CCGGCGGCGGAGGTT | 9690 |
rs751342388 | snp | C/T | 8.49178e-05 | 0.00651549 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170331 | AGAAGTGCATTTGAT[C/T]GCTGTGCTACCTTGT | 9690 |
rs751373768 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169616 | CATGACCTCAAATGA[-/T]TCGCCTGCCTTGGCC | 9690 |
rs751374370 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260570 | GACGACTTTTTATCG[A/G]TAAAGATTTTAATGC | 9690 |
rs751396437 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186721 | TAGATAATTTTGAGA[C/T]GATGCCTAGCTTTCT | 9690 |
rs751435138 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248261 | ACTATGAGGAGAAAA[C/T]ACCTGCTCTCTTAGG | 9690 |
rs751460416 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249207 | TAGCACATTTTCCTC[A/G]GTCTACAGAGCAACC | 9690 |
rs751462335 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183079 | TCTCTCACTCAACAC[C/T]GAAAAATTCTGTGAG | 9690 |
rs751465410 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216042 | AATACTAAGCTGTGA[A/T]GACATAGTGAAGTGT | 9690 |
rs751509163 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204656 | TTTTCAGTACTTGCT[A/G]TTGAAATCAGCCAGT | 9690 |
rs751511256 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177543 | GGCTCTCCCACCGCC[C/T]GCCGCTGCCCTTTGC | 9690 |
rs751521871 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182185 | TTCATTTCATCATTC[C/T]GGCGCTTGCAGATGC | 9690 |
rs751548798 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137943 | TACTCTTACCACACA[C/T]ACACAAAGAGGGTAG | 9690 |
rs751552268 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254436 | GAGTTTCACTCTTGT[C/T]GCCCAGGCTGGAGTG | 9690 |
rs751552996 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158258 | AATATAATGAAGCCT[C/T]TTGAAAACCAGTTTT | 9690 |
rs751557336 | snp | A/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165742 | ATTTCAGTTTTTGTT[A/G/T]TTTCAGTTCTAGAAT | 9690 |
rs751558897 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239512 | ACTAAGTGCTTTTCC[A/G]TAAGTGTGTTCACTG | 9690 |
rs751595172 | snp | A/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227494 | ACAAGGTCAGGAGAT[A/C/T]GAGACCAGCCTGGCC | 9690 |
rs751634266 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250933 | TAATAGTGAAACGTC[G/T]CATATGCAAGAATTC | 9690 |
rs751638668 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152718 | ATCCGGATGCTGTAC[A/G]GCCTCTCCCTCGTGT | 9690 |
rs751643698 | in-del | -/GTAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188311 | TCTTTGAAATGAACT[-/GTAA]GTAAGGAACCCATCG | 9690 |
rs751655679 | in-del | -/ACA | 1.65113e-05 | 0.00287322 | cds-indel, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207715 | AGTTGTAGGTCAAAG[-/ACA]ACAATCATCAATGAT | 9690 |
rs751659604 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267614 | ATTTTGTATTCACAA[C/T]GGAGGCTCCGACCTT | 9690 |
rs751663785 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263307 | GGGCGCCTGTCCTAA[C/T]GCCACCTTCCCGGGC | 9690 |
rs751663938 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190047 | CTCAGGTGATCTCCC[A/G]CCTCAGCTTTCCAAA | 9690 |
rs751667145 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179723 | GCTTTCCTTCACCTG[A/G]AGTCATAGTCTGGGT | 9690 |
rs751685199 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178492 | CCGTTTGGCACATAA[C/T]GAGAATTCTTTTAAA | 9690 |
rs751686683 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140824 | GAATCTCAAGGGAAG[A/T]TAGCACGAGCTGTGT | 9690 |
rs751712634 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218094 | TCTTGAGAAAAAGTC[G/T]TAACTGGATTCATTT | 9690 |
rs751721397 | snp | A/C | 9.90083e-05 | 0.00703522 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220740 | TGGAGGTTCCGGCGG[A/C]TGGGGAGGATAGGCC | 9690 |
rs751740053 | in-del | -/AGGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154081 | TCCCAGCACCTTGGG[-/AGGG]AGGCCGAGGTGGGTG | 9690 |
rs751743622 | in-del | -/TTCT | 1.68437e-05 | 0.00290199 | intron-variant | UBE3C | GRCh38.p7 | 7:157225550 | AAATGGTATATATAA[-/TTCT]TTCTGTGTATTATTT | 9690 |
rs751749572 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208034 | TGCAGGTTTGTTTCA[C/G]ACATGTTTTAATTTG | 9690 |
rs751752921 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246049 | TGTCATTTTCTGAAA[C/T]AAAAAGCCAGTGGTA | 9690 |
rs751791692 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169535 | CATGTGCCACCACGT[C/G]CAGCTGATTTTTGTA | 9690 |
rs751802610 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206940 | GCTTCAATATTGAAT[A/G]GCTTTCAACGTTACC | 9690 |
rs751802669 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218806 | GTTAGGAGCCTGTCT[A/C]TAGCTGGTCATGGGC | 9690 |
rs751846040 | snp | C/G | 3.40861e-05 | 0.00412818 | intron-variant | UBE3C | GRCh38.p7 | 7:157217018 | ATTAAAAAATACATT[C/G]AGCTTGTGTCTTTCT | 9690 |
rs751870791 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245546 | CATTATCAGGAGATG[A/G]TGACTATGTGCCTGT | 9690 |
rs751889907 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208418 | ATTTTAGTACTTTTG[A/C]TTAATTAAGGTAATT | 9690 |
rs751893800 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210631 | TCTGAAAAGAATACA[A/G]ATTGTATCAGCATTT | 9690 |
rs751898918 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211642 | TAAATGGGTTAACAA[A/G]TGGTAACTAAGGGCT | 9690 |
rs751967191 | snp | A/G | 1.67778e-05 | 0.00289631 | intron-variant | UBE3C | GRCh38.p7 | 7:157207666 | TGTGTTAAAAGATGG[A/G]AAAAGAAACAATAGA | 9690 |
rs751996115 | snp | G/T | 1.65029e-05 | 0.00287248 | intron-variant | UBE3C | GRCh38.p7 | 7:157163804 | TTTTTCTCTGTTTGG[G/T]TGTAGGAGGAAAAGG | 9690 |
rs752038326 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231097 | CCTGATTTGAAAAAG[C/T]GGATCCGTGTGCACT | 9690 |
rs752064275 | snp | C/T | 1.69046e-05 | 0.00290723 | intron-variant | UBE3C | GRCh38.p7 | 7:157225555 | GTATATATAATTCTT[C/T]CTGTGTATTATTTGG | 9690 |
rs752086187 | snp | C/T | 2.81916e-05 | 0.00375433 | intron-variant | UBE3C | GRCh38.p7 | 7:157139351 | AAGGTGAGGGCCGGG[C/T]TGGCGGGGCGCCCTC | 9690 |
rs752090851 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214506 | TGATGCAATTAAATA[G/T]GTAAATATGTCAGAA | 9690 |
rs752122032 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162347 | CTACTGGTATGTGCC[A/C]CCATGCCCGGCTAAT | 9690 |
rs752136290 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262248 | TTCTAACATTTTTAT[A/G]AGAGATTTAAAGGAG | 9690 |
rs752230484 | snp | A/T | 1.66123e-05 | 0.00288199 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254297 | GGACCTAAAATCCTT[A/T]ACAAACTATTCAGGT | 9690 |
rs752238975 | snp | G/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174924 | GCTGTTTCAGATATG[G/T]CTGTATCAGAACTTA | 9690 |
rs752239351 | in-del | -/AA | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138106 | CGTATGTGTGGATAT[-/AA]GACACATGTTTATGT | 9690 |
rs752241599 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148246 | GCTGGGCTTACAGGC[A/G]CCCACCACCAGGCCT | 9690 |
rs752252293 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254107 | AATGTCGTCAGCCTC[A/G]AGTGGCTCCGAATGT | 9690 |
rs752295108 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180841 | TTGTGGTCTCCAAAT[A/G]CATCATCTCCTCTAA | 9690 |
rs752326793 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183942 | CTTCCTCTCTCAGTT[A/G]CCAGTCTCTCCTGCC | 9690 |
rs752326861 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant | UBE3C | GRCh38.p7 | 7:157170475 | AACTACATTTTCACT[C/T]GTCCTCGTTTACACG | 9690 |
rs752353708 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265856 | CTGTACCTTTAAATA[C/G]CAGAACGTCATGAAC | 9690 |
rs752404176 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154189 | AGCCAGGTGTGGTGG[C/T]AGGCGGCTGTAATCC | 9690 |
rs752414869 | snp | C/T | 3.3592e-05 | 0.00409815 | intron-variant | UBE3C | GRCh38.p7 | 7:157183840 | TTTTAAAAAATAATG[C/T]TTAACTAAAATACGT | 9690 |
rs752438327 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | UBE3C | GRCh38.p7 | 7:157181709 | GATTTTGTCCTTTCA[C/T]AAGATCTATATCTGA | 9690 |
rs752451503 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233601 | TTTTGTTTACTTACT[C/T]ATCCCAGGCTGGAGT | 9690 |
rs752461627 | in-del | -/GCAGATCC | 1.64925e-05 | 0.00287158 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254049 | CTACAGGCTGAACAG[-/GCAGATCC]GCCAGCACTGCCTGG | 9690 |
rs752461955 | snp | A/G | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231302 | TTGCCAGACATTACT[A/G]CTTCCTAGGCAGAAT | 9690 |
rs752494193 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242861 | GGAGTTCTAGACCAG[C/G]CTGACCAACATGGTG | 9690 |
rs752538646 | in-del | -/GAG | 6.63168e-05 | 0.00575795 | intron-variant | UBE3C | GRCh38.p7 | 7:157169141 | AGTTTGTTTTAAAAT[-/GAG]GAGATTAGTAGGGCA | 9690 |
rs752567215 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170503 | ACGTGTTCTGCTTTT[C/T]TGTTTAAAGTGGAAA | 9690 |
rs752567734 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196513 | TTGTTCTGGAGAAGA[C/T]GTTCTAGGTTGAGCA | 9690 |
rs752586295 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198173 | AAGCAAAATCTGAAC[A/G]TCTTGTAGCTGATTT | 9690 |
rs752587820 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223649 | CATTATTTGGCCAGG[A/T]ACAGTGGCTCATGCC | 9690 |
rs752606257 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196180 | AATGCGGATGTTCTC[C/T]AGAAGGTGGAATGAC | 9690 |
rs752632007 | snp | C/G | 0.000153522 | 0.00875999 | intron-variant | UBE3C | GRCh38.p7 | 7:157201683 | TTTGAATAAGTAATT[C/G]CTTTACTGTTCTGTG | 9690 |
rs752646623 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186597 | AATACTGAAGCTACT[A/G]TTATATCATAGGCAA | 9690 |
rs752670422 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262224 | TTTCTGGTTCTCCTT[C/T]GGTTCTCATTCTAAC | 9690 |
rs752685018 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259731 | GGCTGGAGGTGGCAG[C/T]GGGAGCTTCGGAGAA | 9690 |
rs752743020 | snp | A/C | 5.16916e-05 | 0.00508361 | intron-variant | UBE3C | GRCh38.p7 | 7:157217000 | ATCTTTTTAATATTT[A/C]TCATTAAAAAATACA | 9690 |
rs752757751 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259085 | GGCACTTACCTTATC[A/G]AATCCACTGGCTGCA | 9690 |
rs752789990 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261875 | TCTCACTCTGAATTA[A/T]TGCAAATTCCCGTTG | 9690 |
rs752803356 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200302 | CATTACATTAAAATA[A/G]GAATGGAGTTTAGTT | 9690 |
rs752804602 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260877 | AAGAGCCAGCAATAA[C/T]GTGTGCCTAGGAGTG | 9690 |
rs752816493 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162237 | TCTTGCTGTGTTGCC[C/G]AGGCTGGAGTGCAGT | 9690 |
rs752864401 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150194 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 9690 |
rs752875238 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237120 | AATGGGAGATGTATT[C/T]CTGAATTCAGTTGAT | 9690 |
rs752883213 | in-del | -/A | 1.70429e-05 | 0.0029191 | intron-variant | UBE3C | GRCh38.p7 | 7:157175079 | TATAATGTATTGATC[-/A]CCTTGTCTAGGGGAA | 9690 |
rs752900628 | snp | C/T | 3.67411e-05 | 0.00428593 | intron-variant | UBE3C | GRCh38.p7 | 7:157216834 | GTGCTGCCGAGCTCA[C/T]GTGTGTGACGCGGAT | 9690 |
rs752917690 | snp | A/G | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139867 | CACGCATTTGCTGAT[A/G]TCGATAATCTCTAAA | 9690 |
rs752917825 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151379 | ATTGTCAACATACAT[C/T]TTGGTGAATGTGAGT | 9690 |
rs752918486 | snp | C/G | 0.000163706 | 0.00904579 | intron-variant | UBE3C | GRCh38.p7 | 7:157164495 | TAAGGAGAAAGCTCA[C/G]TGTTAAGACATGTGT | 9690 |
rs752926470 | in-del | -/T | 1.65485e-05 | 0.00287645 | intron-variant | UBE3C | GRCh38.p7 | 7:157201705 | TGTTCTGTGTTTTTC[-/T]CCTATTCCTTTTTAG | 9690 |
rs752927187 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264240 | TGCTCGGCCTGTTAC[-/AC]ACACACACACACACA | 9690 |
rs752927410 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187560 | CTAATTTTTTGTTTT[-/TG]TGTGTGTGTGTGTTT | 9690 |
rs752929992 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250860 | TGAGTGTTGTGGTGA[C/T]CTGCCTGAGGCCTTT | 9690 |
rs752935516 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169140 | AAGTTTGTTTTAAAA[C/T]GAGGAGATTAGTAGG | 9690 |
rs752994955 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208344 | GCCTCCCATAGTGCT[A/G]GGATTATAGGCGTGA | 9690 |
rs752996494 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154925 | GGAACCCTACCCATC[C/T]CTTAGAAATGAAATG | 9690 |
rs753023273 | snp | C/G | 3.31433e-05 | 0.0040707 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182158 | TGGCAGCACCTTTTA[C/G]AGATCAGATTTTTCA | 9690 |
rs753043589 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244124 | AATCCCAGCTGCTCG[C/T]GAGGCTGAGGCAGGA | 9690 |
rs753049383 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143625 | GCCTGGGTCATGTTT[C/T]CACCTGATAACCTCA | 9690 |
rs753050864 | snp | C/T | 8.13416e-05 | 0.00637685 | intron-variant | UBE3C | GRCh38.p7 | 7:157139347 | CAGGAAGGTGAGGGC[C/T]GGGCTGGCGGGGCGC | 9690 |
rs753051707 | in-del | -/TTAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214289 | AATGTAAATGAGAAC[-/TTAA]TTGTCTCATATAATT | 9690 |
rs753076153 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172180 | GGGGTTACAAGCTTA[C/T]GCCACCACCCCTAGC | 9690 |
rs753086789 | snp | G/T | 1.65468e-05 | 0.00287631 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225514 | CATTTATGAAGATGC[G/T]TATGACAAACTTTCT | 9690 |
rs753087242 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221287 | AAGTTTCACTGGGAG[C/T]AAGAATCCTGAGACA | 9690 |
rs753099001 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142626 | ATTCAAAGTCACTTT[G/T]GGGAGCTAAACATTG | 9690 |
rs753118229 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225367 | AGGTTGTAAGAGGTC[C/T]TTTGTTTCTAATAAC | 9690 |
rs753132941 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182678 | TAGTATGTTTGAAAA[C/T]ATACATACATACATA | 9690 |
rs753134967 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193141 | CAGCTTGTCTCCAGA[C/T]GAAATACACCTTAAA | 9690 |
rs753161707 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256999 | AAAGCGCAAACTGCT[A/G]AAGTTTGTAACAAGC | 9690 |
rs753166899 | snp | G/T | 1.65548e-05 | 0.002877 | intron-variant | UBE3C | GRCh38.p7 | 7:157225374 | AAGAGGTCTTTTGTT[G/T]CTAATAACCTTACAG | 9690 |
rs753175101 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210249 | TTTGAAATCAAGTTG[C/T]TGTAAGACCTTTTGA | 9690 |
rs753206627 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170515 | TTTTTGTTTAAAGTG[G/T]AAATGGCTTCTCATC | 9690 |
rs753209035 | snp | A/G | 1.654e-05 | 0.00287571 | intron-variant | UBE3C | GRCh38.p7 | 7:157186825 | ACTGGTTGTTCTGGT[A/G]TGTTCTAGGAGGATG | 9690 |
rs753227369 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223452 | GTGCCTAGTGCCTGG[C/T]TGATTACATAACATA | 9690 |
rs753232798 | snp | G/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178746 | TTCCAATGAGAATGC[G/T]TGAAGTATTTTCGTC | 9690 |
rs753242215 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194461 | GTAGGCATAAAAGAC[-/TT]TTCTAGGTACTTAGA | 9690 |
rs753260584 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244996 | AGTTGTATAATTAAC[C/G]TGTGTTTAGAAAATA | 9690 |
rs753286654 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146305 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 9690 |
rs753292583 | snp | A/G | 3.32215e-05 | 0.00407549 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170356 | CCTTGTCACAGTCCG[A/G]GGGCGCTTTTCCCAT | 9690 |
rs753307702 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172885 | TTGCCTTTGAGTGAG[A/G]TCCTCAATCTTAGTC | 9690 |
rs753322507 | snp | G/T | 1.69499e-05 | 0.00291112 | intron-variant | UBE3C | GRCh38.p7 | 7:157175073 | AACGTATATAATGTA[G/T]TGATCACCTTGTCTA | 9690 |
rs753349610 | snp | A/T | 3.36581e-05 | 0.00410219 | intron-variant | UBE3C | GRCh38.p7 | 7:157183829 | TTCGTTTTCCATTTT[A/T]AAAAATAATGTTTAA | 9690 |
rs753350826 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258871 | AATAACTTCTAAACC[C/T]GCACTGACCAATTGT | 9690 |
rs753371189 | snp | A/G | 5.27264e-05 | 0.00513424 | intron-variant | UBE3C | GRCh38.p7 | 7:157253939 | TTTTGAGATCCTTAC[A/G]TTTTGTATTCCCAGG | 9690 |
rs753411976 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224258 | GGAGTGCAGAGGCGC[A/G]ATCTTGGCTCACTGC | 9690 |
rs753419503 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248089 | GCATTTGTTGGCTTC[G/T]GTCTCACAAGAAGGA | 9690 |
rs753437529 | snp | A/G | 1.66319e-05 | 0.00288369 | intron-variant | UBE3C | GRCh38.p7 | 7:157207599 | CTGGCCACTTGGCCC[A/G]TCAGTTTTCATAGAC | 9690 |
rs753439581 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163563 | ACCTGTACTCATTTG[G/T]ATATGTGAAGAAATC | 9690 |
rs753458978 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175258 | GTATCTTTCAGATGA[C/T]TTTTTCTTTCACGGA | 9690 |
rs753459136 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217693 | AATACAAAAATCAGC[C/T]GGGCGTGGTGGCAGA | 9690 |
rs753494739 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160968 | AACCTTACTGTAATC[A/C]TGAGAGTATTGGAAA | 9690 |
rs753512304 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215816 | AATGCATTTCTATTC[A/G]GTAGAGAACTTCAGG | 9690 |
rs753518911 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197493 | AATTTATCTGTAAAA[A/G]TAATAAAAATAATTT | 9690 |
rs753527109 | snp | A/G | 6.59055e-05 | 0.00574007 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207463 | TTGAAGATTCTAGTC[A/G]AATCATCCCACTCTT | 9690 |
rs753582276 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164690 | TTATTTTAACAATTC[A/G]TTTAGGCCCCTGACA | 9690 |
rs753585750 | snp | A/C | 4.33379e-05 | 0.00465479 | intron-variant | UBE3C | GRCh38.p7 | 7:157188919 | GAGTTAGGATTTGCC[A/C]TTTAATTTCTGTTTA | 9690 |
rs753591248 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241078 | TGGAAGTGGCAGTAA[C/G]GAGCACAGGGGGCCT | 9690 |
rs753591329 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251872 | GGGCGCAGTGGCTCA[C/T]GGCTGTAATCCCAGC | 9690 |
rs753613651 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140731 | GCAGGAACACCCCAC[C/G]GGCCACGGATGTTGG | 9690 |
rs753615093 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217911 | CCCTGTAGTCCCAGC[G/T]ACTCAGGAGGCTAAG | 9690 |
rs753615245 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230841 | GAGGACCAATTCCCT[G/T]AGAGTTTGTGGGGGC | 9690 |
rs753654105 | snp | G/T | 0.000104444 | 0.00722573 | intron-variant | UBE3C | GRCh38.p7 | 7:157223137 | TGTGTTCATGGAACT[G/T]GATTTAGATAAATGA | 9690 |
rs753675661 | in-del | -/T | 7.03631e-05 | 0.00593099 | intron-variant | UBE3C | GRCh38.p7 | 7:157207951 | TATAGAGTATATGTA[-/T]TTTTTTTGTTTACTG | 9690 |
rs753682276 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241892 | AGAATGTTCTGCCCG[G/T]TGAGAGCAGATGCAG | 9690 |
rs753682728 | in-del | -/T | 0.0024023 | 0.0345742 | intron-variant | UBE3C | GRCh38.p7 | 7:157231065 | CTCCTCACCCTCCCA[-/T]TTTTTTTTTAACAGA | 9690 |
rs753698802 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208228 | TACTGGCACATGCCA[C/T]CACACCCAGCTAATT | 9690 |
rs753700200 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206701 | TCAAGCCATTCTCCT[G/T]CCTCAGCCTCCTATG | 9690 |
rs753713429 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233543 | CCTCAACCTCTCAAA[A/G]GGCTAGAATTACAGG | 9690 |
rs753759609 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195491 | CTTGAAACTGAAAGG[A/G]GGGTGCCTGGCTGGT | 9690 |
rs753765446 | snp | A/G | 5.20007e-05 | 0.00509879 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157187000 | TGATGGTGCAGCACC[A/G]CATGATGGTACCCAA | 9690 |
rs753804329 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198178 | AAATCTGAACATCTT[A/G]TAGCTGATTTTCTCC | 9690 |
rs753810727 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184245 | TGTAAATGGAGACAC[A/G]TAGCTTTGTGTTTGG | 9690 |
rs753811008 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267313 | TGTAATCCCAGCTAC[C/T]TGGGAGACTGAGGCA | 9690 |
rs753823270 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243785 | CCCACAATCCGAAAA[A/C]TCTTAACACAAGAAT | 9690 |
rs753835050 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258057 | GGCTGAAGCAATCTG[C/T]CCACCTCAGCCTCCC | 9690 |
rs753835144 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157327 | ACATAAAAATATCAT[A/G]ACCAAGGTTAAAGAG | 9690 |
rs753859825 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221177 | GGTTGAAAGACATTT[A/G]GTTATTTTTTCTGTC | 9690 |
rs753876575 | snp | A/T | 3.33311e-05 | 0.00408221 | intron-variant | UBE3C | GRCh38.p7 | 7:157220780 | CCACCCTGGACGGTG[A/T]GTTCTCTAGGACACA | 9690 |
rs753892543 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172094 | CTGGAGTGTAGTGGT[A/G]CGATCTCAGCTCACC | 9690 |
rs753932775 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243972 | CGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 9690 |
rs753946353 | snp | C/T | 0.000163039 | 0.00902734 | intron-variant | UBE3C | GRCh38.p7 | 7:157164457 | GCCTCGTCTGGCTGA[C/T]GATGTTGATGTTTCA | 9690 |
rs753951824 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143418 | AAGGTCAGAAACACC[C/G]AGATAGCAGGTATCA | 9690 |
rs753984729 | snp | A/T | 1.66131e-05 | 0.00288206 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207873 | AGTATTGGAGTTACT[A/T]CTAGCTCTGAAATGC | 9690 |
rs753989766 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198433 | ACATTAAGTTCTGCA[A/C]ATCCTGTGCGCTCGG | 9690 |
rs754017728 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235256 | TCTTTCTGTTAAAGT[A/G]AGCCCAAGAACCTTC | 9690 |
rs754023466 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148953 | ACTGTCAGGACTGGT[A/G]TTATTTAGCAACACT | 9690 |
rs754036825 | snp | G/T | 1.65367e-05 | 0.00287543 | intron-variant | UBE3C | GRCh38.p7 | 7:157181679 | GGTGCGAGGTGAGAC[G/T]GGAATGGATTTATTG | 9690 |
rs754036901 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163843 | TTACATCGTACTCAG[A/G]AAGAAAGAAGAAAGA | 9690 |
rs754065466 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260775 | TTTGTCAGCTCCTGG[C/T]TAATTAGATAATGCT | 9690 |
rs754069641 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160785 | CTGCAGTGTTTTTCT[G/T]TTTTCTGCTTTTCTC | 9690 |
rs754111682 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240132 | CTTGGCATGGCTCAC[A/T]GCAACCTCTGCCTCC | 9690 |
rs754122622 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181596 | ATTTATCTCGAGTTC[C/T]TATAGCAAAAATTTT | 9690 |
rs754131789 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265205 | AGAGTTTCGTGTACA[C/T]GTGTGCAGGGAAGGG | 9690 |
rs754131974 | in-del | -/T | 1.78717e-05 | 0.00298923 | intron-variant | UBE3C | GRCh38.p7 | 7:157170498 | TTACACGTGTTCTGC[-/T]TTTTTTGTTTAAAGT | 9690 |
rs754134892 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228617 | GCAAGCTGGAGCCAA[A/G]TGGCTTAGATGTGTT | 9690 |
rs754150691 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188040 | CAATAATCTTGAACT[C/G]TTTTCTCTCCCTCCA | 9690 |
rs754157624 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197799 | TGTATCAAACGACTC[C/T]CATCTGCTAACCTGA | 9690 |
rs754175914 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223293 | CTGTGTCTGAGGAAA[A/G]ACAGCTTGCTGTCCT | 9690 |
rs754213519 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205160 | AGCAGAAAGAATGGT[C/T]AGCAGAGAACTAAGA | 9690 |
rs754226070 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253263 | GTCTGTCATACAAGT[A/G]GGGGACAGTAAGACC | 9690 |
rs754226545 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153016 | GCCTAGCCAACATGG[C/T]GAAACCCTGTCTCTA | 9690 |
rs754237940 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181035 | TCTATGAATTCAACA[C/T]GGTGTTTAAAAAATG | 9690 |
rs754310909 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191621 | GTTTTCTAACCATTT[A/C]TTTGCCATGTGTTTT | 9690 |
rs754343076 | snp | A/C/G | 6.62618e-05 | 0.00575562 | intron-variant | UBE3C | GRCh38.p7 | 7:157184057 | CCCTGCATCTGGGGG[A/C/G]CTGCGATGCAGGCAG | 9690 |
rs754384833 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173090 | AGGATAAAAGAAAAG[G/T]GGGCTGGACACAGTG | 9690 |
rs754386726 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254845 | AGGAGTTTGAAACCA[G/T]CCTGGGCAATGTGGC | 9690 |
rs754390625 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225850 | CTGCTCTGCAAAAGG[C/T]TGAGGCGGGAGGATG | 9690 |
rs754403997 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142285 | GCTTAGTGGAAAATG[A/G]AGTGGTTACCACCTT | 9690 |
rs754408951 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171012 | AGATGAGGTCTTGCT[A/G]TGTTGCCCAGGCTGG | 9690 |
rs754410304 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147519 | GTATGCCTTTTTTTT[-/C]CTTTTTTCTTTTCTA | 9690 |
rs754423404 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209505 | GTTAAAAAATAAGCA[A/G]TCTCACCTATTTAAA | 9690 |
rs754441244 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174161 | CGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9690 |
rs754443742 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185257 | AGAACATGCGGACCC[A/G]TGAACCGGGAAATCA | 9690 |
rs754450729 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247910 | TGTTTGGAAATAGGG[G/T]CCAATAGCTGCGAGG | 9690 |
rs754465613 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183971 | CCAGCGCGAGCTGTC[A/G]CGACTCAGCCAGTGA | 9690 |
rs754467284 | snp | A/C | 3.08532e-05 | 0.00392755 | intron-variant | UBE3C | GRCh38.p7 | 7:157207983 | CATTGAAAAATGTAC[A/C]AACTTTTGTCTTGAC | 9690 |
rs754477200 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233348 | TAGGCTGGAGTGCAC[C/T]GCTACAAACACGGCT | 9690 |
rs754483852 | snp | C/T | 5.02163e-05 | 0.00501055 | intron-variant | UBE3C | GRCh38.p7 | 7:157220786 | TGGACGGTGAGTTCT[C/T]TAGGACACAGGGTTA | 9690 |
rs754491152 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213054 | TGAGCCACCACGCCC[A/G]GCAGTGTGTGCATTT | 9690 |
rs754505172 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237989 | CCTGAAATGTAGAGG[A/C]TGCAGTGAGCAGTGA | 9690 |
rs754515935 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214220 | GAAATATGAAAGAGG[A/G]TACACTATATTGAAA | 9690 |
rs754528257 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238618 | AGGGAGGCATTCTTA[C/T]GGAGGCTTAGTGAGG | 9690 |
rs754564797 | snp | A/G | 8.40852e-05 | 0.00648348 | intron-variant | UBE3C | GRCh38.p7 | 7:157183830 | TCGTTTTCCATTTTA[A/G]AAAATAATGTTTAAC | 9690 |
rs754565800 | in-del | -/TTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250209 | TTAGCATATGGGGCT[-/TTG]TTGTTGTTGTTGTTG | 9690 |
rs754579201 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164733 | GAACTTACTATGTAT[A/G]TACTAGGTATTGCTC | 9690 |
rs754605825 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190336 | CCTCTTTCTGTCCCT[C/G]TTTTGGTGAACAGGC | 9690 |
rs754618541 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248275 | ATACCTGCTCTCTTA[C/G]GATTGGGTTTAATAT | 9690 |
rs754640525 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153210 | CTCAAAAACAAAACA[A/G]AACAAAATTGTTCAG | 9690 |
rs754654659 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228655 | TTCCCAAGGGTGACA[C/T]GGACACTGACCCAGA | 9690 |
rs754667155 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207987 | GAAAAATGTACAAAC[-/TT]TTGTCTTGACTCGTT | 9690 |
rs754683621 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206754 | CCTATCACCACACCT[A/G]GCTAATTAATTTAAT | 9690 |
rs754688532 | in-del | -/CG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260556 | GGTGAGGCGTGCAGA[-/CG]CGACTTTTTATCGGT | 9690 |
rs754690774 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239332 | ATTGAGTTGAAGAAT[C/T]CAGACACACAAAAGT | 9690 |
rs754694381 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202783 | ATGCTCATGGTAGTA[A/G]TGATAATAGCAGTCA | 9690 |
rs754697865 | in-del | -/TTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242511 | GAGACTGAGCCTGAG[-/TTG]TTGTTTTTTTTTTTT | 9690 |
rs754697937 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232713 | GATTAATTTCTGTAA[A/G]AATCAGAGCTATAAT | 9690 |
rs754732006 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194183 | TTTTTGAAATGGGGC[A/T]GGCTGTTATACATTA | 9690 |
rs754740060 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231191 | TAAATGAACTACTGA[A/G]GTCAGGATTTAACCC | 9690 |
rs754741950 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193921 | TAATTCTCTCCTAAC[A/G]TAAATCTCTATTTTG | 9690 |
rs754785845 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222748 | GCCAAGTTACGATTT[A/G]TTGTTGGAAAGGAAT | 9690 |
rs754827942 | in-del | -/AG | 3.35649e-05 | 0.0040965 | intron-variant | UBE3C | GRCh38.p7 | 7:157248319 | TGGCTCTTTGTTTGT[-/AG]AAGGCTTGTATATTC | 9690 |
rs754829206 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156423 | GTGATTCTTGTGCCT[C/T]AGCCTTTCAAGTAGC | 9690 |
rs754852756 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233549 | CCTCTCAAAAGGCTA[C/G]AATTACAGGTGTGAG | 9690 |
rs754861439 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145086 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 9690 |
rs754919508 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196382 | TAACTAAGGATGAAG[C/T]GGTGTCTGGGAAGAA | 9690 |
rs754926438 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258083 | CTCCCAAGTAGCTGT[A/G]ACTACAGGCATGTAC | 9690 |
rs754950565 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197995 | TGTATTCTTGATCCT[A/G]ATGGTCCTCCATATC | 9690 |
rs754957074 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157334 | AATATCATAACCAAG[C/G]TTAAAGAGTAACAAA | 9690 |
rs754959664 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224435 | CCTGACCTCGTGATC[-/T]TGCCTGCCCCAGCCT | 9690 |
rs754980184 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146442 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 9690 |
rs754981174 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256176 | GAGGGCGAATCTCAC[A/C]CTGTCACCCAGGCTG | 9690 |
rs754985482 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160559 | GATTGTATCATTTGT[A/G]TGGTACCAAGTAGTA | 9690 |
rs755017421 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237735 | GCTCTTATTTGTGCA[A/G]TAAAGACAACAAATA | 9690 |
rs755051576 | in-del | -/AAAAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235199 | TGTCTCAAATTAAAA[-/AAAAG]AAAAGAAAAGAAAAT | 9690 |
rs755052080 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159837 | AAAAAAATAAATACC[A/G]TTTGCTTGCCTGATC | 9690 |
rs755066372 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259989 | TGAGTTTGTTTCAAA[C/T]AGGTCAATCATCGAC | 9690 |
rs755066915 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230694 | AGGCAGACCCCGTCT[-/C]AAAAAAAAAAAAAAA | 9690 |
rs755075986 | snp | G/T | 3.73965e-05 | 0.00432398 | intron-variant | UBE3C | GRCh38.p7 | 7:157216819 | GGCTCACTGTGCATT[G/T]TGCTGCCGAGCTCAC | 9690 |
rs755083822 | snp | C/T | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183972 | CAGCGCGAGCTGTCA[C/T]GACTCAGCCAGTGAC | 9690 |
rs755121759 | snp | A/G | 0.000326797 | 0.0127786 | intron-variant | UBE3C | GRCh38.p7 | 7:157164487 | ATGAAGCATAAGGAG[A/G]AAGCTCACTGTTAAG | 9690 |
rs755126653 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208137 | TGGAGTGCAATGACA[C/T]CATCATACTCCACTG | 9690 |
rs755149574 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198443 | CTGCAAATCCTGTGC[G/T]CTCGGAGGCCACAGC | 9690 |
rs755171873 | snp | C/G | 1.66147e-05 | 0.0028822 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186911 | GCAGCAGACCAACAC[C/G]CTGCTCAACCTGGTG | 9690 |
rs755179664 | in-del | -/TT/TTTT | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137559 | GCGGCGCCAGGACTG[-/TT/TTTT]TATTTCTTTTTTTTT | 9690 |
rs755182843 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149044 | AGTTCCCTGCTATAG[A/G]TAAGGTTAAGAATTC | 9690 |
rs755192643 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257947 | TTTTTTCCTTTTTTC[-/T]TTTTTTTTTTTTTTA | 9690 |
rs755213822 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163856 | AGGAAGAAAGAAGAA[A/G]GAGAGAGGTAAAAAC | 9690 |
rs755226824 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188106 | AACAGAAAAGTATTC[A/G]ATTGGATACAGAGTA | 9690 |
rs755229206 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216208 | TGATATCTGGGGTGC[C/T]GCTTTTTTCCCCTAG | 9690 |
rs755238006 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150082 | TTATAACAGATTTAT[C/T]AAGAGTCTAACAAGG | 9690 |
rs755244400 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249431 | AGTGATTCTCCTGCC[C/G]CAGCTTCCCGAGTAG | 9690 |
rs755259671 | snp | G/T | 3.30929e-05 | 0.0040676 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207705 | TTGTGTTTTTTAGTT[G/T]TAGGTCAAAGACAAT | 9690 |
rs755269737 | in-del | -/CG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174577 | CCCATCTCAGCCTCT[-/CG]AATAGCTGGGACTAC | 9690 |
rs755270074 | in-del | -/G | 1.65831e-05 | 0.00287945 | intron-variant | UBE3C | GRCh38.p7 | 7:157174912 | ATTTTATGTTTTGCT[-/G]TTTCAGATATGGCTG | 9690 |
rs755272277 | snp | A/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138119 | ATAAGACACATGTTT[A/T]TGTATAGGTGGTCCC | 9690 |
rs755289436 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222267 | ATATTTTGTCCCAAT[C/T]TGTGGCTTGTCTTTT | 9690 |
rs755309907 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219107 | GCTCTGGTGAAGGAG[A/G]TGACCAGGGCGGTGC | 9690 |
rs755319681 | snp | C/T | 1.656e-05 | 0.00287745 | intron-variant | UBE3C | GRCh38.p7 | 7:157225366 | TAGGTTGTAAGAGGT[C/T]TTTTGTTTCTAATAA | 9690 |
rs755336556 | snp | A/T | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256981 | AGGGTTCACTGATGA[A/T]GAAAAGCGCAAACTG | 9690 |
rs755342612 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219657 | CTGTAATCCCAGCAC[G/T]TTGGGAGACCGAAGT | 9690 |
rs755373088 | snp | A/G | 3.29636e-05 | 0.00405964 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223294 | TGTGTCTGAGGAAAG[A/G]CAGCTTGCTGTCCTG | 9690 |
rs755399692 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220100 | CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGG | 9690 |
rs755433666 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208929 | AATGCTAGATTTACA[G/T]TCCGTTTAATACCAG | 9690 |
rs755434039 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195467 | GTGAGCTGAAGATTA[-/C]TCCCAGGCCTTGAAA | 9690 |
rs755437167 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268401 | TTTGGAGATACTGTC[G/T]GTGGATGTGAGGTGG | 9690 |
rs755550417 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195359 | ATAAAAGAAGAAACA[A/G]ACTGATAAGCTGATA | 9690 |
rs755554001 | in-del | -/CTTTTTTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158042 | CCCAATCTGTACACT[-/CTTTTTTC]CTTTTTTTTTTTTTT | 9690 |
rs755568346 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257879 | AATAATATATAATTA[G/T]ATAAGTACTGTATGT | 9690 |
rs755571467 | snp | C/G | 9.89087e-05 | 0.00703168 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174950 | ACTTAATTAAACACA[C/G]CTCTCTGTTTGTCAA | 9690 |
rs755612301 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183581 | TTCTGGTGAAAAGCC[C/G]CATTCTGAGTCCCCT | 9690 |
rs755635215 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184171 | CCGTCAGCCCCACTA[C/T]CACAGTTTCTAGTGA | 9690 |
rs755656547 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144969 | AGCGTTATACAGAAG[A/G]GTGTCATTGCCCTAG | 9690 |
rs755659794 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246854 | TTGACCTGGGAAAAT[A/G]GGATCACTGTAAATA | 9690 |
rs755664052 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222595 | CAGCTAATTTTTAAA[A/G]AAATTTTCTTCGTAG | 9690 |
rs755669710 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146191 | CCAACTCCATTGAAT[A/G]CCTGCCTTTGCTCCT | 9690 |
rs755683339 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214659 | CGAACATCTTCATAC[-/A]AAAAGATTGTACTTC | 9690 |
rs755733142 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201152 | AACGTTGTGAAACCT[C/T]ATCTCTACTAAAAAT | 9690 |
rs755736922 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182200 | CGGCGCTTGCAGATG[C/T]GCAGACCGTTTTCCC | 9690 |
rs755748234 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211878 | GCATTCAGCTAATGA[C/G]AGTGGGAAACAGCAA | 9690 |
rs755751969 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223420 | TTAACACACACCCAC[C/T]AGAGAAATCTCTAAA | 9690 |
rs755836860 | snp | A/G | 6.10407e-05 | 0.00552419 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139222 | CCCCGTGCCCCGCCC[A/G]CCCGGCTGCTTCCGC | 9690 |
rs755840421 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152092 | GACAGCATGGGCAAA[A/G]CTGTCCAACCATGGA | 9690 |
rs755843441 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228677 | TGACCCAGAGGTGGC[A/G]GGCACGGCAGGGCAG | 9690 |
rs755876073 | snp | C/T | 2.23731e-05 | 0.00334456 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186982 | CCTCCGTCTGCCACA[C/T]GCTGATGGTGCAGCA | 9690 |
rs755879135 | snp | A/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178537 | CTGAATGTTAGTTGG[A/G/T]TGATTTCCCTGTCTA | 9690 |
rs755913924 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253451 | TTATCACTGATCGTT[-/C]ACCACCACCCTTTGT | 9690 |
rs755932483 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177688 | CTGGCTGGGTGTCCT[A/G]CCCAGCCTGCCCGCT | 9690 |
rs755981105 | in-del | -/T | 1.69945e-05 | 0.00291496 | intron-variant | UBE3C | GRCh38.p7 | 7:157181504 | AATTTTAAATATGTG[-/T]TTTTTCCTTTTAGGG | 9690 |
rs756019628 | snp | A/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242794 | AGGTCTGGTGGCTCA[A/C/T]GCCTGTAATCCCAGC | 9690 |
rs756023561 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240980 | GGGGCAGTGACTGAA[C/G]CCGGGAGAGGTAATG | 9690 |
rs756034325 | snp | G/T | 6.66089e-05 | 0.00577062 | intron-variant | UBE3C | GRCh38.p7 | 7:157220658 | TGTGCTAGAGCACAG[G/T]GGAGTTCTGAACCAG | 9690 |
rs756072745 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167685 | GGGACTATAGGCACC[C/T]GCCACCATGCCCGGC | 9690 |
rs756105774 | snp | C/T | 0.000390424 | 0.0139664 | intron-variant | UBE3C | GRCh38.p7 | 7:157253934 | GAGGATTTTGAGATC[C/T]TTACGTTTTGTATTC | 9690 |
rs756107668 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232413 | GCCCAGGCTGGAGTG[C/G]TGTGGCGCCATCTCT | 9690 |
rs756114150 | snp | C/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256970 | AGAGTTGTGGAAGGG[C/T]TCACTGATGAAGAAA | 9690 |
rs756118291 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194734 | AGGAATATGTTATTG[A/G]AAAACTGGAGGAAAA | 9690 |
rs756128317 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156235 | TGGGTGATCATTCAG[A/T]TGGGAATGTAAACAG | 9690 |
rs756140517 | in-del | -/ATC | 1.64757e-05 | 0.00287012 | cds-indel, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207792 | GATGCATGCCTGGGG[-/ATC]ATCAAGTTGGCTTAT | 9690 |
rs756162380 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268474 | GGAGAGCTTTCAGGG[G/T]AGGTGGAGGAGGAGG | 9690 |
rs756201660 | in-del | -/TAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220053 | CATCTCTACAAAAAG[-/TAC]TACAAAAATTAACCA | 9690 |
rs756213887 | snp | G/T | 1.64947e-05 | 0.00287177 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163827 | GGAAAAGGCTTCTCT[G/T]TTACATCGTACTCAG | 9690 |
rs756225026 | snp | A/T | 1.84232e-05 | 0.003035 | intron-variant | UBE3C | GRCh38.p7 | 7:157139370 | CGGGGCGCCCTCGGC[A/T]CGGGGCCTGCGCGGC | 9690 |
rs756242360 | snp | A/G | 1.66907e-05 | 0.00288879 | intron-variant | UBE3C | GRCh38.p7 | 7:157207681 | AAAAAGAAACAATAG[A/G]AAACTGGATTGTGTT | 9690 |
rs756262595 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242884 | ACATGGTGAAACCCC[A/G]TCTCTACTCAAAATA | 9690 |
rs756268390 | snp | A/G | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181581 | GTATTGAATATTCTG[A/G]TTTATCTCGAGTTCC | 9690 |
rs756301481 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231177 | TTTCAGAGAGTTTTT[A/G]AATGAACTACTGAAG | 9690 |
rs756312692 | snp | C/T | 1.72558e-05 | 0.00293728 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267758 | TGAGCTGAGCTGAAG[C/T]TGATGCTGGGGTCAG | 9690 |
rs756354190 | snp | C/G | 1.66286e-05 | 0.0028834 | intron-variant | UBE3C | GRCh38.p7 | 7:157178866 | AGTAGTAGGCAGGAT[C/G]AGAACTGTGGCTCAG | 9690 |
rs756355075 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158718 | CTGAACTCAGCTAAT[C/T]CTTTGCTTTGTCAGG | 9690 |
rs756374289 | snp | A/G/T | 3.7492e-05 | 0.00432953 | intron-variant | UBE3C | GRCh38.p7 | 7:157223205 | ATTGTCAGTGGGAAT[A/G/T]CAGGGGAAAGTACAA | 9690 |
rs756385383 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197880 | AGTATTGATTTATCC[A/T]CCTCTTCTGGAGAGG | 9690 |
rs756411526 | snp | A/G | 1.692e-05 | 0.00290856 | intron-variant | UBE3C | GRCh38.p7 | 7:157254331 | TTATCACTGCTAGTT[A/G]TTGTTTCTGAAAATG | 9690 |
rs756424379 | snp | A/G | 3.43991e-05 | 0.00414709 | intron-variant | UBE3C | GRCh38.p7 | 7:157225577 | ATTATTTGGCAGGTG[A/G]AGGCTAGGGAATTGT | 9690 |
rs756431361 | snp | G/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174933 | GATATGGCTGTATCA[G/T]AACTTAATTAAACAC | 9690 |
rs756467815 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189755 | TGTGGGTTCTTTTTT[-/C]TCCTCTTTCTCACTC | 9690 |
rs756497609 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162444 | ATGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 9690 |
rs756537357 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264973 | TTTCCTCATGTTATT[C/G]TTTGAGATATTTTTA | 9690 |
rs756550636 | snp | A/G | 0.000162986 | 0.00902587 | intron-variant | UBE3C | GRCh38.p7 | 7:157164447 | GGCGTGAACTGCCTC[A/G]TCTGGCTGATGATGT | 9690 |
rs756551757 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190888 | CCATTGCGCTTTTTT[A/G]TGCCTCCATGGTGTT | 9690 |
rs756557682 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218267 | CCTGGGCAACATGGT[C/T]AAACCCAGTCTCTAC | 9690 |
rs756563685 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190194 | CATTTGTGTCTTTAG[G/T]TTAAGTAACTTTCTG | 9690 |
rs756585211 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179839 | GCCTTGCTGCTTGGC[A/G]TGTTACTATTTTTTA | 9690 |
rs756586208 | snp | C/T | 3.53033e-05 | 0.00420124 | intron-variant | UBE3C | GRCh38.p7 | 7:157170489 | TTGTCCTCGTTTACA[C/T]GTGTTCTGCTTTTTT | 9690 |
rs756632990 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140955 | TTGAGGAGGAAGGGC[G/T]AGAGGGAAGCTGGGT | 9690 |
rs756678763 | snp | A/G | 1.65187e-05 | 0.00287386 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183879 | ATTGTTTTGCAAAGG[A/G]GCCCTCTCTGAGGAA | 9690 |
rs756692650 | snp | C/T | 4.9445e-05 | 0.00497193 | intron-variant | UBE3C | GRCh38.p7 | 7:157201820 | AGGGTATGTATTATA[C/T]AGACTTATAAATTGA | 9690 |
rs756722294 | snp | A/G | 9.90393e-05 | 0.00703632 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207848 | AGAAGAATATATTAC[A/G]GCATTTCAGAGTATT | 9690 |
rs756731182 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267133 | TAATTTTTTAAAAAA[A/G]CAAATGTGGGCCAGG | 9690 |
rs756731921 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243927 | TGTTGTATTTGGACT[C/T]TTGCATTAAAGATGA | 9690 |
rs756736758 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144871 | TATTAATTGAAGTCC[-/AT]ATAGTGTACATTCAG | 9690 |
rs756736969 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253131 | TATTGTATTTTGCTC[A/C/G]TGTACTGTTTTGTAT | 9690 |
rs756772781 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255225 | ATAAGCACACAATAA[C/T]GATGTTCAGCATCAT | 9690 |
rs756777741 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196568 | AGTGAGTTTCCTAGA[A/G]AAATGTGTTGAATGA | 9690 |
rs756798080 | snp | C/G/T | 0.000148303 | 0.00860996 | intron-variant | UBE3C | GRCh38.p7 | 7:157182065 | GTGATTGGATGGACA[C/G/T]TATAATTTGATTTTA | 9690 |
rs756800086 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230891 | GATCGTGCCACTGCA[C/T]TCCAGCCTGGGTGAC | 9690 |
rs756833301 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183502 | TCCAGTGTCCCTCCC[A/G]CAGACAGCCCCTTGG | 9690 |
rs756844136 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143856 | AGAGGACTTGGAGTT[C/T]GGGACAGGGTGGGAC | 9690 |
rs756866021 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210682 | AATTTGAGTTGAAGA[A/T]TTCGAGGTAGAATCA | 9690 |
rs756935672 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156017 | TATGAGTACAATAAA[G/T]TGAAACCAAAAACTT | 9690 |
rs756946162 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144788 | CTCACCTCACTTTTC[C/T]CTATTACTAGCATCT | 9690 |
rs756952754 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163625 | TAACTTGTATTATAT[C/T]TAGTGACCTCTGGGA | 9690 |
rs756963211 | snp | A/G | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223273 | TTTGGAGTCCCCGCC[A/G]CTGTCTGTGTCTGAG | 9690 |
rs756976544 | snp | C/G/T | 1.71334e-05 | 0.00292684 | intron-variant | UBE3C | GRCh38.p7 | 7:157225574 | TGTATTATTTGGCAG[C/G/T]TGGAGGCTAGGGAAT | 9690 |
rs756985981 | snp | A/C | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138552 | GCACCCCACCCTGCA[A/C]CCCGCACCCTGCCCT | 9690 |
rs756992382 | in-del | -/CAAAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153197 | AGTGGGACTCCCTCT[-/CAAAAA]CAAAACAAAACAAAA | 9690 |
rs757024206 | snp | C/T | 1.66382e-05 | 0.00288424 | intron-variant | UBE3C | GRCh38.p7 | 7:157184073 | CTGCGATGCAGGCAG[C/T]CCCGTCGGATCTTCT | 9690 |
rs757032160 | snp | A/G | 7.43909e-05 | 0.00609835 | intron-variant | UBE3C | GRCh38.p7 | 7:157217049 | GGAGAGAAGAATTAA[A/G]CACTTTAAAATTATT | 9690 |
rs757035782 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148901 | ACTCCAGGCTTGCCA[C/T]TACCCAACCCCAGCC | 9690 |
rs757095865 | in-del | -/AAAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173209 | CAGACCCCACCTGTA[-/AAAC]AAAGCAAAAAATAAA | 9690 |
rs757110014 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216070 | TGTGTCCAGGCCAGC[C/G]TGTTTGGAAAGGTTA | 9690 |
rs757113137 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248533 | GACGATGTGGAGGAG[C/T]TTGGGCTGAACTTCA | 9690 |
rs757129965 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177749 | TGCGGCTGTTGAGAC[A/C]GAAGGCAGCCTGCGG | 9690 |
rs757147780 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249222 | GGTCTACAGAGCAAC[A/C]GTGCACCCATTAGCA | 9690 |
rs757162615 | snp | A/T | 1.65051e-05 | 0.00287267 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248370 | TTCTCTTTTGAAGGC[A/T]CTCTATGAGAACATG | 9690 |
rs757192527 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203713 | ACAAATCTTATTAAA[-/AG]ACAGTTTGATAATTT | 9690 |
rs757194277 | snp | A/G/T | 6.6616e-05 | 0.00577098 | intron-variant | UBE3C | GRCh38.p7 | 7:157169158 | GGAGATTAGTAGGGC[A/G/T]TGGGAGAGCTTATTT | 9690 |
rs757204391 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137977 | TTTCACAATGTCTCT[A/G]TGAAATCATCATGTT | 9690 |
rs757207200 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154398 | CCCTAACTTCCCACC[A/G]TTATTTTCTCAGTAT | 9690 |
rs757216989 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177559 | GCCGCTGCCCTTTGC[A/G]TCCCAGCGGCTTGTT | 9690 |
rs757232697 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154397 | CCCCTAACTTCCCAC[A/C]ATTATTTTCTCAGTA | 9690 |
rs757248172 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178509 | AGAATTCTTTTAAAA[A/C]CTGTCTGAATGACTG | 9690 |
rs757269080 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241175 | TGAGGATCACAGAGC[A/G]CTGCAGGGCATGTGG | 9690 |
rs757282605 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265977 | TCATGCATTTGGTCT[A/G]TAGATGTTCTACCTC | 9690 |
rs757286256 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182189 | TTTCATCATTCCGGC[A/G]CTTGCAGATGCGCAG | 9690 |
rs757342575 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179783 | CTTGGTCCTCTTGGT[C/T]CTCTGTCAAAACTAC | 9690 |
rs757399548 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264464 | TGCTCGGCCTGTTAC[-/AC]ACACACACACACACC | 9690 |
rs757431788 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242076 | AAATTGATTGTGGCG[A/T]TGGTCATACAACTTT | 9690 |
rs757441159 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242068 | ATCTTCAGAAATTGA[C/T]TGTGGCGATGGTCAT | 9690 |
rs757470564 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218027 | GATTCTGTCTCCAGA[A/G]AAAACAAAAAATATA | 9690 |
rs757479666 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207011 | TGATTTGCCTTTATT[A/G]AATATGTTGAGTAGA | 9690 |
rs757493820 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233673 | TTTTAGCTATTGTGA[A/G]TAATGTTACTGCAAA | 9690 |
rs757498613 | snp | A/G | 6.70995e-05 | 0.00579182 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253972 | GTTGAACTAAAATTC[A/G]GTGGGAAAGACATCC | 9690 |
rs757501128 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169590 | CACGTTGACCAGGCT[A/G]GTCTGGAACTCATGA | 9690 |
rs757503922 | snp | A/G | 3.29766e-05 | 0.00406045 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186867 | GTATCATACATAACA[A/G]AGGAATGCCTGAAGA | 9690 |
rs757522203 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195649 | AGGTTCGCAAGTGCA[C/T]AGATGGAGGAGAATT | 9690 |
rs757531589 | snp | C/T | 3.29864e-05 | 0.00406105 | intron-variant | UBE3C | GRCh38.p7 | 7:157257059 | GGTACACAACTTTCA[C/T]GACATTTGCTTTAAA | 9690 |
rs757561903 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267438 | AAGAAAACAAACAAC[-/A]ACAACAAAGCAAATG | 9690 |
rs757591614 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211716 | ATACTTCATGACTTT[C/G]ATAGGTTAGAGTGTT | 9690 |
rs757604972 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157407 | AGATGAAAAGATAAT[C/T]AAATGAAAAAATTAA | 9690 |
rs757622286 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236312 | TTATTGAGGTTAATC[C/T]TTTATCATATTTGAA | 9690 |
rs757647997 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173047 | AAACCTGAAATAGAA[C/T]TAAATGTCATAAGAC | 9690 |
rs757648798 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183543 | GTGGGGCTGAAAGTT[C/G]CAACCCTCTGATCAC | 9690 |
rs757650699 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237529 | GGTCTTGCTTACTAT[A/T]GAGTTATTCCTTCCT | 9690 |
rs757675495 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252439 | ATGGAATTGAAAGCC[C/T]ATTCTTAGGCTTGAT | 9690 |
rs757675928 | snp | C/T | 3.30775e-05 | 0.00406665 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182324 | TGTTGGCGAAAATTA[C/T]TTGGGTATGAAATAC | 9690 |
rs757703075 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161118 | TAGAACAGATAAACA[A/G]CATCAGTGGGAAAAT | 9690 |
rs757728644 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226932 | TGACTCCTAATCTAA[C/G]TAATCGTCTAATTGA | 9690 |
rs757741519 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189182 | GCCGAGGAAGCTGGG[C/G]CTGGAGCAGAAGTGC | 9690 |
rs757742502 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250934 | AATAGTGAAACGTCG[C/T]ATATGCAAGAATTCC | 9690 |
rs757767681 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150522 | TTATGGCATTACTTA[C/T]AATACTGAAAAATAC | 9690 |
rs757783426 | in-del | -/CTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235506 | AGGATAAACTCATTT[-/CTC]CTCTGTTTATTGACA | 9690 |
rs757786152 | snp | G/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207490 | TCTTTTATCTTTTTA[G/T]CTCCTTGTTTAGTCA | 9690 |
rs757786923 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262309 | AATGGATTTTAGCAC[A/C]TATTATATGCCACAT | 9690 |
rs757835135 | snp | C/T | 3.22898e-05 | 0.00401794 | intron-variant | UBE3C | GRCh38.p7 | 7:157139362 | CGGGCTGGCGGGGCG[C/T]CCTCGGCTCGGGGCC | 9690 |
rs757849844 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189608 | GCGGTGCCCACTCAG[C/T]CCCGCGGCATTCCTG | 9690 |
rs757859886 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164889 | TTAGAGATGGTGTTT[A/C]GGGGAAGGGCTCTCT | 9690 |
rs757868975 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231098 | CTGATTTGAAAAAGC[A/G]GATCCGTGTGCACTT | 9690 |
rs757870338 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231010 | TCCTTAAGCCTTCCT[A/G]TAAGGCTAGTTGATG | 9690 |
rs757877885 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203373 | CTTTCATTTCCAAAC[A/C]AAAATACAAGATTTT | 9690 |
rs757892083 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247861 | CCCCAAAACTGTGCT[C/T]AAATCCTAATACCCC | 9690 |
rs757916861 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198894 | GTGATTTAGTAAATA[C/T]TCTGTCAGGGTTAGC | 9690 |
rs757919566 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265436 | TCAGAGGACCGACAC[A/G]CCCATAGGTCTCATG | 9690 |
rs757934547 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267922 | AATGATTTTTATTAC[A/G]GTGTGGTCACTTATT | 9690 |
rs757958852 | snp | A/G | 3.98668e-05 | 0.00446451 | intron-variant | UBE3C | GRCh38.p7 | 7:157188952 | ACTGATTGTCAGGGT[A/G]TACAAATGAATGTGG | 9690 |
rs758022270 | snp | A/C | 3.24839e-05 | 0.00403 | intron-variant | UBE3C | GRCh38.p7 | 7:157223177 | GATGATTTCAAGAAT[A/C]TTCACCTTAAGAATT | 9690 |
rs758022338 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220203 | GTGACAGAGTGAGAC[C/T]GTGTATCAAAAAATA | 9690 |
rs758072468 | snp | C/T | 1.75029e-05 | 0.00295823 | intron-variant | UBE3C | GRCh38.p7 | 7:157170481 | ATTTTCACTTGTCCT[C/T]GTTTACACGTGTTCT | 9690 |
rs758097164 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255148 | TATATACATACACAA[C/T]GTACATGGGCAAAAA | 9690 |
rs758101581 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191784 | TTGTTTTTCATTGTA[C/T]GTGTAGAATTAAATA | 9690 |
rs758115610 | in-del | -/TGT | 1.6697e-05 | 0.00288933 | intron-variant | UBE3C | GRCh38.p7 | 7:157254217 | AAAATTTACCTCAAA[-/TGT]TATTATTTGAACTTT | 9690 |
rs758131910 | snp | A/G | 6.65425e-05 | 0.00576774 | intron-variant | UBE3C | GRCh38.p7 | 7:157248345 | ATATTCGATGCTAAC[A/G]TTGTCACTGTTCTCT | 9690 |
rs758135401 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196866 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 9690 |
rs758148798 | snp | G/T | 1.69453e-05 | 0.00291073 | intron-variant | UBE3C | GRCh38.p7 | 7:157220798 | TCTCTAGGACACAGG[G/T]TTACTGAGGTATGAA | 9690 |
rs758158507 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223693 | CTTTGGGAGGCCGAG[A/G]CAGGTGGATCGAGCC | 9690 |
rs758182526 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229925 | GTTTTAATTTATTTA[-/TT]TTTTTTTTTTTTGAG | 9690 |
rs758186052 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213129 | TTTATTTAATGTAAC[A/G]TTTTGATCTGGCGTG | 9690 |
rs758193345 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210708 | AATCAACCAAAGAAC[G/T]CAGAAGCGTTTAGCC | 9690 |
rs758208715 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | UBE3C | GRCh38.p7 | 7:157163888 | GTTTTGTAATACTCT[A/G]TAGATAAGCATTTTT | 9690 |
rs758211106 | snp | C/T | 3.32094e-05 | 0.00407475 | intron-variant | UBE3C | GRCh38.p7 | 7:157169000 | GCAAAATGTCATTTT[C/T]ACTGGATTCTGACCA | 9690 |
rs758260495 | snp | A/C | 3.32005e-05 | 0.00407421 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231324 | AGGCAGAATGCTTGG[A/C]AAGGTAAAGTAACCT | 9690 |
rs758293966 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256811 | AGAAGGGACTTGAGG[A/C]TCCATGGACTTTAGT | 9690 |
rs758299134 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | UBE3C | GRCh38.p7 | 7:157181717 | CCTTTCACAAGATCT[A/G]TATCTGATGGTAACT | 9690 |
rs758325602 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186617 | ATCATAGGCAAAAAC[C/T]GGGTATTCAGAGTTT | 9690 |
rs758343356 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188313 | TTTGAAATGAACTGT[A/G]AGTAAGGAACCCATC | 9690 |
rs758351149 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147433 | GGTTTTTTGGTTGAT[A/G]CTTGGAATTTCCTGC | 9690 |
rs758408906 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158219 | TTAACTTGGAGGCTG[C/T]GAAGAAAATTCAAAG | 9690 |
rs758440686 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157257022 | TAACAAGCTGCTCTC[A/G]ACCCCCTCTCTTGGG | 9690 |
rs758457713 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248210 | GGATCCTGGAGCACA[A/G]TACCTGCCCACTGAA | 9690 |
rs758464378 | snp | A/G | 1.65943e-05 | 0.00288043 | intron-variant | UBE3C | GRCh38.p7 | 7:157184067 | GGGGGGCTGCGATGC[A/G]GGCAGCCCCGTCGGA | 9690 |
rs758472744 | in-del | -/GGCGGACCCTGCACT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149528 | TCAGGTTCATGCACA[-/GGCGGACCCTGCACT]GGCACATCCCTGAGA | 9690 |
rs758481207 | in-del | -/CTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158050 | GTACACTCTTTTTTC[-/CTT]TTTTTTTTTTTTTTT | 9690 |
rs758484645 | in-del | -/T | 1.70685e-05 | 0.00292129 | intron-variant | UBE3C | GRCh38.p7 | 7:157178680 | TGAATACTTTTTTCA[-/T]TTTTTACAGGTTGCT | 9690 |
rs758493946 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261886 | ATTAATGCAAATTCC[C/T]GTTGTACTGTATTTA | 9690 |
rs758499022 | in-del | -/T/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198532 | CTGGCTGTATTTGTC[-/T/TT]TTTTTTTTTTTATTT | 9690 |
rs758521131 | snp | G/T | 1.69507e-05 | 0.0029112 | intron-variant | UBE3C | GRCh38.p7 | 7:157175074 | ACGTATATAATGTAT[G/T]GATCACCTTGTCTAG | 9690 |
rs758553740 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139871 | CATTTGCTGATGTCG[A/T]TAATCTCTAAAGTAG | 9690 |
rs758555865 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228143 | ATGCTTTACGATGCT[C/G]GTTGTCTTATCTCCG | 9690 |
rs758572408 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264299 | TGCTTGGCCTGTTAC[-/AC]ACACACACACACACA | 9690 |
rs758639239 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151523 | ATGTGCCCTCCTGAT[C/T]ATGTGCTGGCTTTTC | 9690 |
rs758642391 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241094 | GAGCACAGGGGGCCT[A/G]CCTCCCTTCTGTGCC | 9690 |
rs758664754 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173445 | CTGCCCCAGTCTTCA[C/T]ATTGTTTGCCTTCTA | 9690 |
rs758697490 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141759 | TTGAACTTCAGGGGC[A/G]TGGAGCCACTCACCA | 9690 |
rs758702291 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217944 | ATGAGAATCCCTTGT[G/T]CCCTGGAGGCGGAGG | 9690 |
rs758702707 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243539 | AGGGCACCTGCCAGT[A/G]GAGTATTAGAGTGAG | 9690 |
rs758736337 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182219 | GACCGTTTTCCCTTA[C/T]GAGCCCTTTCTGAAT | 9690 |
rs758738398 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207477 | CGAATCATCCCACTC[C/T]TTTATCTTTTTAGCT | 9690 |
rs758761256 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267378 | AGTGAGCTGAGATGG[C/T]GCCATTGCCCTCCAG | 9690 |
rs758764587 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245087 | TCCATTTAGCTGATG[C/G]AATCATAGTTTTTAG | 9690 |
rs758767933 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217837 | AGCGAAATTCCGTCT[C/G]AAAAAAAGAAAGAAA | 9690 |
rs758768124 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221376 | GCACGGCTTTGCATT[C/T]AGACCAGCAATGAAT | 9690 |
rs758794125 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182687 | TGAAAACATACATAC[A/T]TACATACATGCATGA | 9690 |
rs758821556 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164604 | GTTTCTTTAAATAGC[A/T]TTATTTTGTTGATTA | 9690 |
rs758828721 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172900 | GTCCTCAATCTTAGT[C/T]ATCAGTCACGACATG | 9690 |
rs758829506 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210448 | CTATCTCTATTATGA[A/T]GTTGTATGAACTTAC | 9690 |
rs758842734 | in-del | -/TTAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254398 | ATTTTAATTAATTTA[-/TTAA]TTTATTTTTTTTTTT | 9690 |
rs758852324 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236411 | TCAGATTATTTGATA[G/T]GATCTTGGTTATATA | 9690 |
rs758874316 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235509 | ATAAACTCATTTCTC[C/T]TCTGTTTATTGACAT | 9690 |
rs758900785 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204977 | TCTCAAGATCTAGAC[-/AG]AGGTTAGGGATTGCC | 9690 |
rs758905242 | snp | C/T | 0.000108696 | 0.0073713 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139237 | GCCCGGCTGCTTCCG[C/T]GGCGGCGCTGCCCGC | 9690 |
rs758926058 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198510 | CCGCCGCCCTCCGCC[A/G]TCTTCCGCTGGCTGT | 9690 |
rs758947932 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224265 | AGAGGCGCGATCTTG[A/G]CTCACTGCAACCTCC | 9690 |
rs758949192 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149113 | CCAGGCTGGAGTGCA[A/G]TGGCTCAATCTCGGC | 9690 |
rs758981691 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204359 | GACGAGATTGCGCCA[C/T]TGCACTCCAGCCTGG | 9690 |
rs758988758 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147286 | TTTATTTTTAAGGGG[G/T]GCTAATGTGAATGGT | 9690 |
rs759039817 | in-del | -/TTTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229314 | TTTTGGTTTTGGATT[-/TTTG]TTTGTTTGTTTTTTG | 9690 |
rs759041063 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183931 | GTGCTGCAGACCTTC[C/T]TCTCTCAGTTACCAG | 9690 |
rs759063076 | snp | A/G | 8.25702e-05 | 0.00642482 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254098 | GGCCTTGCCAATGTC[A/G]TCAGCCTCGAGTGGC | 9690 |
rs759095744 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251993 | ACAAAAAACTGAGCC[A/G]GGCGTGGTGATGTGC | 9690 |
rs759100609 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198145 | CTAAACTGAAACCAT[C/T]GCTCCACAGTTTAAG | 9690 |
rs759115708 | snp | C/T | 3.30175e-05 | 0.00406296 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231257 | TTCTGTACCCCAACC[C/T]GGCTGCTCAGATGCT | 9690 |
rs759130893 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207775 | TGTCTCGATGCCTTC[A/G]AGATGCATGCCTGGG | 9690 |
rs759158124 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148075 | TCTAGGGCCTACCAA[A/T]ACCAATTACTATAGT | 9690 |
rs759175965 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227210 | TAGAGAAGAGTGAGA[A/T]GTTTAACCTTGAAGG | 9690 |
rs759182058 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176245 | CCAGTTTGGGCAGCA[A/G]AGCAAGACCATGTTT | 9690 |
rs759196619 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260430 | TTTGAAGCATGACCC[A/G]TGTGACCAGATAGGA | 9690 |
rs759205778 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179614 | AGGACTCCTGGGCTC[C/G]AGAAGTATTTGTCAG | 9690 |
rs759215946 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202385 | AAGCCGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 9690 |
rs759216686 | snp | A/T | 3.33178e-05 | 0.00408139 | intron-variant | UBE3C | GRCh38.p7 | 7:157207605 | ACTTGGCCCATCAGT[A/T]TTCATAGACAGTAGA | 9690 |
rs759220641 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170672 | ATAGGCTTTTTCGTA[-/T]TTTTTTGCAGTGGAA | 9690 |
rs759238996 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177359 | TTGTCTCTTGACAAT[A/G]TGGATATCCTTTTCC | 9690 |
rs759265560 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215029 | TAAACATTTCCACTC[A/G]TTGAAGAAGGACGGT | 9690 |
rs759284528 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249017 | TTTTGTTACTTATAT[C/G]CTTTTTAAAAAAGAA | 9690 |
rs759291261 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137807 | CACTTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC | 9690 |
rs759307010 | snp | C/G | 1.65211e-05 | 0.00287407 | intron-variant | UBE3C | GRCh38.p7 | 7:157163794 | CTTACCTCCTTTTTT[C/G]TCTGTTTGGGTGTAG | 9690 |
rs759353206 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174996 | TGAGAGACTTACATG[C/G]TTATTTCAGATAAAA | 9690 |
rs759358330 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228902 | CACGTGTACATAGCA[A/G]TCTAGGGATAGACAG | 9690 |
rs759369094 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252768 | AAAACTGAAGGCTGT[A/G]AAAAGAAAAGAATGG | 9690 |
rs759401231 | snp | C/T | 6.90489e-05 | 0.00587534 | intron-variant | UBE3C | GRCh38.p7 | 7:157223382 | TCTTTATTGTCACTA[C/T]GTATCATATTAGTGT | 9690 |
rs759409127 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242857 | GTCAGGAGTTCTAGA[C/T]CAGCCTGACCAACAT | 9690 |
rs759418046 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208336 | CTGCTTCTGCCTCCC[A/G]TAGTGCTGGGATTAT | 9690 |
rs759427258 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142003 | CAGTTTCCCCGTGTC[A/G]CACGCCCACAGCATC | 9690 |
rs759432547 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165502 | TTCCAGGTTCAAGCG[A/C]TTCTCCTGCCTCAGC | 9690 |
rs759446173 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219323 | GGCACAAGTCCCTTA[C/T]CTCATCACCAGCTGG | 9690 |
rs759454404 | snp | G/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223257 | AATGTGTTTTAGTGG[G/T]TTTGGAGTCCCCGCC | 9690 |
rs759458495 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140612 | ACAAGTTCGGAAGGT[A/C/G]AGCTGCAGAACATTT | 9690 |
rs759461286 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235837 | ATATCTGATGACCAT[A/C]TGATTACAGAGTTAA | 9690 |
rs759504685 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257335 | GCAATATTAATAATG[C/T]CTCATAAATCTGTAA | 9690 |
rs759519325 | snp | A/G | 3.30011e-05 | 0.00406195 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184023 | AGCCGACAAGCCCTC[A/G]AGCCCGGTAAGCCCC | 9690 |
rs759522934 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155828 | GTTGGCTGTGCTCAC[-/TG]TGGATTTCACATTGG | 9690 |
rs759537194 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183817 | AAAAATGGCGTCTTC[A/G]TTTTCCATTTTAAAA | 9690 |
rs759537982 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170727 | ATATTTTGCCCACCT[A/G]TCATGTACCCTGACA | 9690 |
rs759553277 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232314 | CTCTACCTGTTAGGG[C/T]GACATTTATAAAGTT | 9690 |
rs759565162 | snp | A/C | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174919 | GTTTTGCTGTTTCAG[A/C]TATGGCTGTATCAGA | 9690 |
rs759577255 | snp | A/G | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254271 | GGTGCACAAGTTCCC[A/G]TAAGCCTAGAGGACC | 9690 |
rs759591090 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171353 | GGCTAGCCTCCAACT[C/T]CTGGCCTCAAGTGAT | 9690 |
rs759595116 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant | UBE3C | GRCh38.p7 | 7:157169127 | GAAAACAGCAAGTAA[A/G]TTTGTTTTAAAATGA | 9690 |
rs759653432 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200159 | TTGGAAAGATGGCTG[A/G]GCTGAATGATCTAAT | 9690 |
rs759656132 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268807 | TTGCAGTAGGCACTT[C/T]ATCAGGACCTGACCT | 9690 |
rs759661771 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173774 | ACGAACTACATGTCA[A/G]ATGGTGAAGGGAGTA | 9690 |
rs759662761 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144291 | ACACAGCATGACCCC[A/C]TCTCTTAAAAAATAA | 9690 |
rs759663358 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172868 | TCTCTCCAGAGCACC[G/T]ATTGCCTTTGAGTGA | 9690 |
rs759698886 | snp | C/G | 3.3077e-05 | 0.00406662 | intron-variant | UBE3C | GRCh38.p7 | 7:157181681 | TGCGAGGTGAGACTG[C/G]AATGGATTTATTGAT | 9690 |
rs759704185 | snp | G/T | 1.67494e-05 | 0.00289386 | intron-variant | UBE3C | GRCh38.p7 | 7:157248327 | TGTTTGTAGAAGGCT[G/T]GTATATTCGATGCTA | 9690 |
rs759721772 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155862 | GGTAGTTACAGCAGG[A/G]AGCGTGCACGCTGTC | 9690 |
rs759742030 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212413 | AATGTCACAATTTAG[A/G]ATTAATAGCCTTGTC | 9690 |
rs759747642 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236343 | TTCTATTTGAAAATG[C/G]CTTTTTTTCTTGCTT | 9690 |
rs759799050 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162123 | TGTTAGTTCATGTAT[C/T]AGTGTATAATTTTAA | 9690 |
rs759806506 | in-del | -/A | 6.0015e-05 | 0.00547758 | intron-variant | UBE3C | GRCh38.p7 | 7:157187047 | GTGGGCGTCTGTGCC[-/A]GGGGGTGCCAGCCAG | 9690 |
rs759826283 | snp | A/G | 3.29554e-05 | 0.00405914 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201776 | CATCTTTGGTTTCTA[A/G]TATCTTCCATGTCAA | 9690 |
rs759846166 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241440 | GGGACTGGCAGCAAG[A/C]AAATGGGCCATTGGT | 9690 |
rs759855330 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208092 | TTTTTTTTTTTTTTT[-/G]GATACATGGACTTGA | 9690 |
rs759878284 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230849 | ATTCCCTGAGAGTTT[A/G]TGGGGGCGGAGGTTG | 9690 |
rs759898960 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154826 | GTCAGACTTTATTTT[A/T]AAAAATGAGCTCTTG | 9690 |
rs759901322 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239610 | ACAAGAGGAAGGATC[A/G]GAGAAGAATTGGGGG | 9690 |
rs759921146 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170190 | GGACCGATAATGGTG[A/T]TTTCGTTGTCAATTT | 9690 |
rs759968260 | snp | C/T | 2.44311e-05 | 0.00349499 | intron-variant | UBE3C | GRCh38.p7 | 7:157216997 | AAGATCTTTTTAATA[C/T]TTATCATTAAAAAAT | 9690 |
rs759972207 | snp | A/G | 5.33993e-05 | 0.0051669 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186941 | GTGGAGGGACTCTGC[A/G]AGCGAGGAGGTCTTC | 9690 |
rs759974245 | snp | C/G | 9.91359e-05 | 0.00703975 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178716 | ACTGTAATGATGACA[C/G]TTTGAATGTTGCACT | 9690 |
rs759975838 | in-del | -/TG | 1.64779e-05 | 0.00287031 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223279 | GTCCCCGCCGCTGTC[-/TG]TGTCTGAGGAAAGAC | 9690 |
rs760029206 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205340 | ATTACCCTGTCCCTT[C/T]TTTTTTTGGACCCAA | 9690 |
rs760032996 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167313 | AATCCCACAGTGTGT[C/G]TGTTAGTCTCAGCTT | 9690 |
rs760035182 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191653 | TAAGAACTGTGGTGT[A/G]TGTGGTGGGGATGAA | 9690 |
rs760044392 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221249 | GGTTTTTCTGTGAAC[A/G]TACATTTTGTTTGAC | 9690 |
rs760059768 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | UBE3C | GRCh38.p7 | 7:157186817 | TTATGGAGACTGGTT[A/G]TTCTGGTATGTTCTA | 9690 |
rs760072477 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224464 | CTCCCAAAGTGCTGA[A/G]ATTACAGGCATGAGC | 9690 |
rs760079244 | snp | G/T | 1.77871e-05 | 0.00298215 | intron-variant | UBE3C | GRCh38.p7 | 7:157170296 | ATTTTGTTTTGTTTT[G/T]CTTCCAGTATTCCAT | 9690 |
rs760088565 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192822 | GCTTCAACAAACCAG[A/G]AGACAAGTAACTGCG | 9690 |
rs760140644 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208148 | GACACCATCATACTC[C/T]ACTGCAGCCTTGAAC | 9690 |
rs760153153 | in-del | -/TTTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222420 | ACTTTACTTTTTTTT[-/TTTC]TTTCTTTCTTTTTTG | 9690 |
rs760165925 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163465 | TCCTCTGGGGTAATA[C/T]TTTACAAAGCTAGTA | 9690 |
rs760184769 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143582 | TTTGATCATAATTAC[C/G]AGTTTTCAGGAGAGG | 9690 |
rs760201352 | snp | A/G | 2.32356e-05 | 0.00340841 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139327 | GTGTCCCTTGGCGGC[A/G]CGAGCAGGAAGGTGA | 9690 |
rs760219091 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237025 | GCGTGAGCCAGCACA[C/G]CCGGCAAGACAGTTT | 9690 |
rs760230467 | snp | G/T | 3.30224e-05 | 0.00406326 | intron-variant | UBE3C | GRCh38.p7 | 7:157231069 | CTCACCCTCCCATTT[G/T]TTTTTAACAGAGCCT | 9690 |
rs760232623 | snp | C/T | 4.94287e-05 | 0.00497111 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207461 | TTTTGAAGATTCTAG[C/T]CGAATCATCCCACTC | 9690 |
rs760232796 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196223 | AATTCTCCTATGCAA[C/T]GCTGCCGACAAACTG | 9690 |
rs760239488 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253475 | CTTTGTATCGTAATT[-/A]AAAGTGCTTTATAGT | 9690 |
rs760267081 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259419 | CGTTGGGAGTGTACA[C/G]ATGGCAACATATTTT | 9690 |
rs760298595 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234184 | AAGAACGAACATTTT[A/T]AATTTTGAAGTCTAA | 9690 |
rs760312743 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258747 | TTACAGGTATGAGCC[A/G]TCATGCCCGGCCCCC | 9690 |
rs760313042 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158165 | CCAAAGTGATGGAAT[C/T]ACAAGTGTGAGCCAC | 9690 |
rs760339548 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185166 | TTGTATTCATGTGAA[A/G]ATGAGGCTGTGGGCT | 9690 |
rs760345102 | in-del | -/CT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228189 | TGTGCATGTTAGCCC[-/CT]GTTACCCATAAGTTG | 9690 |
rs760355390 | snp | A/T | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225472 | TCCATTTCTGGATGG[A/T]ATTAATGTCACAATA | 9690 |
rs760370872 | snp | C/T | 1.70705e-05 | 0.00292147 | intron-variant | UBE3C | GRCh38.p7 | 7:157174882 | AAACTATTAAATTTT[C/T]ATTGAGAGTTGTATA | 9690 |
rs760400593 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247495 | TCAGGAGTTTGAGAA[A/G]AGCCTGGCCAATATG | 9690 |
rs760415555 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224256 | CTGGAGTGCAGAGGC[A/G]CGATCTTGGCTCACT | 9690 |
rs760439973 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153262 | GCTGTGTGAGCAGAC[A/G]CTAGATTGTTGGCAG | 9690 |
rs760452037 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198103 | GAGCATTTGTTGGTT[C/T]ATTGTAAGGTCTCAA | 9690 |
rs760452392 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178821 | TGTCAGTGATTGAAC[A/G]AATTTTGCACTACAT | 9690 |
rs760484109 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267234 | CAAGACCATCCTGGC[C/T]AACGTGGTGAAACCC | 9690 |
rs760498634 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227415 | TTTAAAACTACTCCC[G/T]GGGCGTGGCGCAGTG | 9690 |
rs760503473 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180674 | TGAAAGAATATATGA[-/T]TTGGATCATTCTTGA | 9690 |
rs760536242 | snp | G/T | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254258 | GGTATTAATTTCTGG[G/T]GCACAAGTTCCCATA | 9690 |
rs760546697 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218500 | TCGAGGAGAGAAAAC[A/G]GGAGTGTTTCAGAAC | 9690 |
rs760549243 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251783 | TTTTAAGTACACATA[A/G]TTGTTTAGGCTTAGC | 9690 |
rs760563107 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241723 | ACAAATTCTCACAAC[A/G]GCATTATTCCTAATA | 9690 |
rs760583643 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141313 | CACATCAAAGGAAGA[C/T]CATCCCCAGCATTCC | 9690 |
rs760588606 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217877 | AAATACAAATATTAG[C/T]CGGGCATGGTAAGTG | 9690 |
rs760591056 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140712 | CGCGCGGCCTCTGTT[A/G]CAGGCAGGAACACCC | 9690 |
rs760593131 | snp | G/T | 3.32923e-05 | 0.00407983 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170416 | TAAGGCAGCTTCTGT[G/T]TTTTTACAAACAAAA | 9690 |
rs760615855 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227921 | TTGAAATCTTTATAA[A/G]TGTTCTCAACTCAAA | 9690 |
rs760622994 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206622 | GAAACAGAGTCTGGC[A/T]CTGTTCCCCAGGCTG | 9690 |
rs760639395 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252583 | TCTGTATAAAATGAG[A/G]ACCAGCAAACGAGTC | 9690 |
rs760681825 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212522 | CTTATGATCATCATT[G/T]CCATGAACTCTCAAA | 9690 |
rs760685233 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179206 | TTACCACCTCCTGGT[C/T]ATTCTGAGTGAATGG | 9690 |
rs760694673 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230771 | CATTCAAAGCCATCC[C/T]GAGCCACATCGGCCT | 9690 |
rs760728382 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190701 | GCATTCTCTTGAACA[-/GT]GTAGACTCCCTTTGC | 9690 |
rs760736283 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217246 | TTCTTTGTGAGGTTG[A/G]AAAATATTTTGCTTT | 9690 |
rs760742492 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180429 | TCACTAGTTATCAGT[A/G]TACACTAGGTTAGAC | 9690 |
rs760754064 | snp | A/C/G | 0.000150381 | 0.00867003 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182146 | CAGAGGAGTTTCTGG[A/C/G]AGCACCTTTTACAGA | 9690 |
rs760755389 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219583 | ATTATGGGAAATTTT[A/C]CAGGATGAAAGTTTC | 9690 |
rs760832260 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182207 | TGCAGATGCGCAGAC[C/T]GTTTTCCCTTACGAG | 9690 |
rs760834841 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254497 | TTGCCTCCCGGGTTC[A/G]AGCAATTCTCCTGCC | 9690 |
rs760834996 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142247 | ATGTCTTAAATTATT[A/G]TTTGAAATCTTCCCT | 9690 |
rs760863322 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154732 | ATGATTGCGTTTTGC[A/G]TTGGATACTTCATTT | 9690 |
rs760878491 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183260 | CCACTTCAGAGGCCG[A/T]TTACAAGTAGTAGGT | 9690 |
rs760880570 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171974 | GGCCACCCATAGTGC[C/T]GGGATTACAGGCATG | 9690 |
rs760890195 | snp | A/G | 3.72169e-05 | 0.00431359 | intron-variant | UBE3C | GRCh38.p7 | 7:157189000 | CATGGAAAGATTTCC[A/G]AGACAGATGCGTACA | 9690 |
rs760913537 | snp | A/T | 1.75755e-05 | 0.00296436 | intron-variant | UBE3C | GRCh38.p7 | 7:157188914 | TTTCAGAGTTAGGAT[A/T]TGCCATTTAATTTCT | 9690 |
rs760922010 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147885 | GCGTATCTGGAATAA[A/C]TCCCACTTGACTGTG | 9690 |
rs760926403 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243690 | AGTGTTGCGGGAGTT[A/G]ATGGTGTAGAAAGCT | 9690 |
rs760926595 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256064 | CACGGTTCTTCAAAA[C/T]AAGGCTCCTCTGCAG | 9690 |
rs760935731 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172769 | TCTGGAACAGGATGT[C/T]CTGGCCTCACATACT | 9690 |
rs760959953 | snp | C/T | 8.28137e-05 | 0.00643428 | intron-variant | UBE3C | GRCh38.p7 | 7:157223230 | GTACAAGTGAACTAA[C/T]TAAGGTTTTAAAATG | 9690 |
rs760964739 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243049 | GAAAGAGGGAAACTC[C/T]ATCTCAAAAAAAAAA | 9690 |
rs760979066 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186135 | GATTTTAAAAAATTC[A/G]TTAATAGGCTGGGAG | 9690 |
rs760983265 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157934 | GCAGTGAGCCAAGAT[A/C]GTGCCACTGCACTCC | 9690 |
rs761050736 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175212 | TAGGTGATTCAGGCC[A/G]GCATGAGGTATAAAT | 9690 |
rs761062433 | in-del | -/TGG | 1.80039e-05 | 0.00300027 | intron-variant | UBE3C | GRCh38.p7 | 7:157170275 | CAAATACTATATTTA[-/TGG]GTCATTTTGTTTTGT | 9690 |
rs761066149 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174856 | AAATTTGGGGTATTA[C/T]GTAAATTAGCAAACT | 9690 |
rs761083129 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239264 | CACAAGACTTACTGA[A/G]TGAACAGACTACAGC | 9690 |
rs761121204 | snp | G/T | 1.6577e-05 | 0.00287893 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216884 | TATCACCAATCTAGT[G/T]AAAATGTTGAAGTCC | 9690 |
rs761127906 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137424 | TAAACATGCCACCAT[A/G]CTCAGCTAATTTTTG | 9690 |
rs761130106 | snp | A/G | 4.94882e-05 | 0.0049741 | missense, intron-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157169075 | AGGTTGAAAAATGCA[A/G]TAATTATCCAGTCAT | 9690 |
rs761135021 | snp | C/G | 0.000162986 | 0.00902587 | intron-variant | UBE3C | GRCh38.p7 | 7:157164440 | GATTACAGGCGTGAA[C/G]TGCCTCGTCTGGCTG | 9690 |
rs761164174 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215224 | CTGTCCACGGGTAGG[C/T]CATTCAAGGGGTGTC | 9690 |
rs761174669 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239867 | GGTGCAGCTGCATGA[C/G]CTGGGGAGCAGGAGC | 9690 |
rs761175845 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239307 | TATGAGTGAACGGCA[C/T]AGACCTAACATTGAG | 9690 |
rs761202296 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240922 | TCACCAAAAATTATC[A/G]CCAGAGTGTGTTGGA | 9690 |
rs761222014 | in-del | -/TGG | 0.000171165 | 0.00924951 | intron-variant | UBE3C | GRCh38.p7 | 7:157182366 | ACCTGAACACACATA[-/TGG]TGGGTAGCATTGGCA | 9690 |
rs761234706 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203991 | TCAAACACTAGGCCA[A/G]TTTTATAATAAAGTG | 9690 |
rs761266323 | snp | C/G | 3.35779e-05 | 0.00409729 | intron-variant | UBE3C | GRCh38.p7 | 7:157231374 | GGACCAAAAGATGTT[C/G]ACATTTTATGTTTAT | 9690 |
rs761294181 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265723 | TTTAAACCTAAAGGA[A/G]GGAGAACATTTTCTC | 9690 |
rs761295522 | in-del | -/G | 1.65029e-05 | 0.00287248 | intron-variant | UBE3C | GRCh38.p7 | 7:157163806 | TTTCTCTGTTTGGGT[-/G]TAGGAGGAAAAGGCT | 9690 |
rs761304721 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222170 | CCACTGCACACTGCC[-/T]TGTGAACATGTTTTT | 9690 |
rs761314279 | snp | A/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241704 | TTTACCCAAAAACTT[A/G/T]CACACAAATTCTCAC | 9690 |
rs761317693 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263154 | CAGCACAAGCTTCTT[C/T]GTAGTTCTAGCCTTT | 9690 |
rs761322686 | in-del | -/AAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161315 | TTTAAAAAATTAAAG[-/AAT]ATTAAGTAAACAATC | 9690 |
rs761332821 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142400 | GAAGTTGATAATCTT[C/G]TTGGGCAGATAAGAC | 9690 |
rs761358828 | snp | A/G | 3.295e-05 | 0.00405881 | intron-variant | UBE3C | GRCh38.p7 | 7:157267567 | ACAGTGACATCTTGC[A/G]CACATGCTGTTTTTC | 9690 |
rs761379764 | snp | A/C | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225435 | TGATTTATGCAGATA[A/C]GCAAGAAGTTCAAGG | 9690 |
rs761419322 | snp | A/G | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269715 | ACTTTCTGCTTTCTG[A/G]TAATTTTGTACACAA | 9690 |
rs761442205 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156038 | CCAAAAACTTGTTAA[A/T]CAATAGGAAGTTCAG | 9690 |
rs761447397 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241605 | CCTCATGCATTGCCA[A/G]TGGGAAGATAAAATG | 9690 |
rs761481263 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256961 | GTCTTCTGGAGAGTT[C/G]TGGAAGGGTTCACTG | 9690 |
rs761486120 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268111 | CTCCTGAGCAGGCAG[C/T]GCCACTCCAGGGTTC | 9690 |
rs761495583 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156831 | TAGATCTACCACATT[C/T]CTTTAAAGAGCTATA | 9690 |
rs761498083 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257645 | GGGAGGCTGAGGCAC[A/G]AGAATTGCTTGAACC | 9690 |
rs761498929 | snp | A/T | 1.81529e-05 | 0.00301266 | intron-variant | UBE3C | GRCh38.p7 | 7:157253918 | CCTATTATCATACTT[A/T]GAGGATTTTGAGATC | 9690 |
rs761510894 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168679 | AAAACATCATGCTAA[A/G]TGAAGAAAACCAGAC | 9690 |
rs761535215 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147444 | TGATACTTGGAATTT[-/C]CTGCACAGATAATCA | 9690 |
rs761569613 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249835 | GAGTTAGTAACATCT[G/T]GGATTTGCTTCAAAT | 9690 |
rs761578147 | snp | C/T | 1.67486e-05 | 0.00289379 | intron-variant | UBE3C | GRCh38.p7 | 7:157175049 | GGTAAAATTCTATTG[C/T]AAGTCAGTAACGTAT | 9690 |
rs761593061 | snp | C/T | 3.30229e-05 | 0.0040633 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207550 | TCTTCGGTGATCCCA[C/T]AGAAGGTAAGGATTT | 9690 |
rs761604701 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179734 | CCTGAAGTCATAGTC[C/T]GGGTTACATCTAACG | 9690 |
rs761681007 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250762 | TCATTAGGAAGTACT[C/T]GACATCCAGTGATGT | 9690 |
rs761689352 | snp | A/G | 5.07971e-05 | 0.00503944 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170332 | GAAGTGCATTTGATC[A/G]CTGTGCTACCTTGTC | 9690 |
rs761689742 | snp | A/G | 1.72276e-05 | 0.00293487 | intron-variant | UBE3C | GRCh38.p7 | 7:157182368 | CCTGAACACACATAT[A/G]GGTAGCATTGGCAGA | 9690 |
rs761714452 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146377 | GCTAGGATTACAGGT[A/G]TGCACCACCACACCT | 9690 |
rs761716244 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187981 | CAGACAAAACAAAAC[A/C]TGCAAGTTAAAAATA | 9690 |
rs761736081 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173186 | GAGACCAGCCTGGCC[-/A]AAAATACCAGACCCC | 9690 |
rs761737995 | in-del | -/TTAT | 1.69701e-05 | 0.00291287 | intron-variant | UBE3C | GRCh38.p7 | 7:157225563 | AATTCTTTCTGTGTA[-/TTAT]TTGGCAGGTGGAGGC | 9690 |
rs761753934 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150006 | GTGGTCAAATTACAG[C/G]CTGTAATACCTGCTG | 9690 |
rs761778094 | snp | C/T | 9.00394e-05 | 0.00670907 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139308 | CTTCAAGACGCGGCC[C/T]AAGGTGTCCCTTGGC | 9690 |
rs761779177 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182280 | AGAAAGAGTGGTGGA[A/G]CACCCTGGCTTTTCT | 9690 |
rs761779670 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185021 | AGTATTCATTTTTTT[-/G]TATGTTTATAAAAAA | 9690 |
rs761808023 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188675 | TTGATTTTATGAGTA[C/T]AGCACCTATTTCCTC | 9690 |
rs761810702 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196010 | TTACTATGGATTTCA[A/T]GACGAGGCGATAAGC | 9690 |
rs761824000 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263860 | CCCATTCTAACCATT[A/T]TTTTTTTATGTTTCC | 9690 |
rs761835839 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207438 | ATATCCAGGGGTTCT[C/T]CTATGTCTTTTGAAG | 9690 |
rs761855495 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238978 | TAGCACTGAGAAGTG[G/T]CCATGTCATTTAGCA | 9690 |
rs761857529 | in-del | -/AAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192830 | AACCAGAAGACAAGT[-/AAC]AACTGCGTATGAGTT | 9690 |
rs761870898 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252953 | TCTTGCTTTATCTCA[A/G]ACTCCTGGGCTTAAG | 9690 |
rs761879903 | snp | A/G | 1.71971e-05 | 0.00293227 | intron-variant | UBE3C | GRCh38.p7 | 7:157187066 | GGTGCCAGCCAGAGA[A/G]CATACCTTCCTCCCT | 9690 |
rs761898332 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190747 | TCACATTCCTTGGAT[C/T]ATTGATTTGTGCAGT | 9690 |
rs761924551 | snp | C/T | 3.37359e-05 | 0.00410692 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267733 | ATGCGATTGAATGTG[C/T]CGCTGGCTTTGAGCT | 9690 |
rs761933789 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228171 | CCGAACGATTCTCTG[C/T]AGTGTGCATGTTAGC | 9690 |
rs761967751 | snp | A/G | 4.20239e-05 | 0.00458369 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186972 | ACCACCATGGCCTCC[A/G]TCTGCCACACGCTGA | 9690 |
rs761971432 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264813 | CTGACCTCAGGTGAT[C/G]CACCCGTTGTGGCCT | 9690 |
rs761984719 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152730 | TACGGCCTCTCCCTC[A/G]TGTCTGGGCAGGTTG | 9690 |
rs761987137 | in-del | -/G | 1.73543e-05 | 0.00294565 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267766 | GCTGAAGCTGATGCT[-/G]GGGTCAGACCCCTAC | 9690 |
rs761991321 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170787 | TCAGTGGGACGTGCA[C/T]CCTGAATACCACATC | 9690 |
rs762015826 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212206 | ATCTACTGTAGAAAG[-/A]AAAAAAAAAATTAAC | 9690 |
rs762022976 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180691 | TGGATCATTCTTGAT[A/G]CCCAGAGTTATGTTC | 9690 |
rs762074411 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181723 | ACAAGATCTATATCT[G/T]ATGGTAACTTTTACA | 9690 |
rs762077357 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258577 | CAATTCTCCTGCCTC[A/G]GCCTCCTGAATAGCT | 9690 |
rs762091748 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185057 | GGTTCTGTAGATGGA[A/C]TGTAGATAAATTTTT | 9690 |
rs762124356 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212778 | TTTTTTGTTTTTCTT[C/T]TTGAGACAGGGTTTC | 9690 |
rs762125312 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137323 | GCTCATTGCAACCTC[C/T]GCCTCGCAGACACAA | 9690 |
rs762140527 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155104 | ACCTGTAAGTATGTT[C/T]TGCATTTGTGAAATT | 9690 |
rs762153475 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162914 | AAGAGGGTTCTGTTT[A/T]AGTATTTTTCATTTA | 9690 |
rs762173797 | snp | A/T | 1.65932e-05 | 0.00288034 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170407 | CCCTTTTGGTAAGGC[A/T]GCTTCTGTTTTTTTA | 9690 |
rs762187435 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145901 | CATTTGTGACATTGG[A/G]GAACTATTGAATTTT | 9690 |
rs762208941 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207800 | CCTGGGGATCATCAA[G/T]TTGGCTTATCCAGAA | 9690 |
rs762216663 | snp | C/T | 1.66991e-05 | 0.00288951 | intron-variant | UBE3C | GRCh38.p7 | 7:157223146 | GGAACTGGATTTAGA[C/T]AAATGAGTTAATCAG | 9690 |
rs762263640 | snp | C/G | 1.67153e-05 | 0.00289091 | intron-variant | UBE3C | GRCh38.p7 | 7:157231360 | TAAAAATAGACCTCG[C/G]ACCAAAAGATGTTGA | 9690 |
rs762282141 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230049 | AAGTAGCTGGGATTA[A/C]AGACATGTGCCACCT | 9690 |
rs762322506 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187636 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 9690 |
rs762322610 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215724 | CTTGAGCTCTGTAGT[A/G]GTTATATGATCCAAT | 9690 |
rs762342700 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247914 | TGGAAATAGGGTCCA[A/G]TAGCTGCGAGGCCTT | 9690 |
rs762344285 | snp | C/T | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181659 | CTTACAACTCCTGTC[C/T]GGAAGGTGCGAGGTG | 9690 |
rs762360890 | snp | C/T | 3.63432e-05 | 0.00426266 | intron-variant | UBE3C | GRCh38.p7 | 7:157188985 | ACCTTTGTACCCTGA[C/T]ATGGAAAGATTTCCG | 9690 |
rs762364672 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213772 | ATATTCTAAATAAGT[A/G]TTTTGGGAATTGGTC | 9690 |
rs762378001 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177485 | TTACCTCTCACATGG[A/G]ATTATCAGCACACAT | 9690 |
rs762397901 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226336 | TCACTGGCACGTTTC[A/G]TCGTATGTTCATATT | 9690 |
rs762419858 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164093 | GCTTTTGGTTGACTT[-/A]ACATAATGATATGGT | 9690 |
rs762431482 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192585 | CTTGTGTTGAGACTT[C/T]GTGGTGGTGCTAAGA | 9690 |
rs762450063 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164075 | GACTGGAGAAGGAAC[A/G]TGGGCTTTTGGTTGA | 9690 |
rs762478449 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251195 | AGTTTTTAAGTTTAT[-/A]AAGTATGATTTAAAG | 9690 |
rs762501759 | in-del | -/TTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146663 | TATATTAAACTAAAC[-/TTTT]TTTTAATTTGAGAGG | 9690 |
rs762504001 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146569 | ATTCTCTCCTCCATT[-/G]GATCTCTCTCCCTTT | 9690 |
rs762519781 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261025 | CCAAATAGACTGGCC[A/G]GGTGCGGTGGCTCAC | 9690 |
rs762533937 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188540 | TGCTTTTATTGTCGC[A/G]CAACCCATTGCTGTG | 9690 |
rs762539804 | snp | C/T | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223269 | TGGGTTTGGAGTCCC[C/T]GCCGCTGTCTGTGTC | 9690 |
rs762547730 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249183 | AGCCATCATCACCCT[A/C]GCCAATGTTAGCACA | 9690 |
rs762559112 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144495 | TAACTTTCAGAGTCT[G/T]CGAGAATACCCGAGA | 9690 |
rs762562903 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216610 | TTTCAAAGCTTAATC[G/T]CCACCTCCGTTGTAA | 9690 |
rs762633130 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250396 | TGCCCTGTGTTACCC[A/G]GGTTGATCTCAAATT | 9690 |
rs762635968 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167506 | ACCTGTAAGATGACT[G/T]TGCATTTGTATATAA | 9690 |
rs762652946 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205516 | GGCTCCAGCTGTCAT[A/G]GGCAGGGCTGTTGAA | 9690 |
rs762654754 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178053 | AAAGGATTGGGGTGG[A/G]GGGAAAGAGGGAGGA | 9690 |
rs762658508 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239409 | TCCTTGCAGTTTTTG[G/T]AAGGCAGGATCCTGA | 9690 |
rs762662315 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230478 | AAGGCGGGCAGATCA[C/T]AAGGTCAGGAGTTCG | 9690 |
rs762689579 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183944 | TCCTCTCTCAGTTAC[C/T]AGTCTCTCCTGCCAG | 9690 |
rs762723137 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240690 | GGAAATTAATCCGTG[A/G]ATGGAGATTTGAGGG | 9690 |
rs762749095 | snp | C/G | 1.65111e-05 | 0.0028732 | intron-variant | UBE3C | GRCh38.p7 | 7:157225398 | CTTACAGCTTTCCTT[C/G]TTTGTTAGATCTTTC | 9690 |
rs762753684 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140367 | GAGGTTAGAAGGGAA[C/T]CTGGGTAAAGAGTTG | 9690 |
rs762769121 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220901 | TCCCAGCAGGAGCTA[C/T]CATGTAGAAAAGTTT | 9690 |
rs762785873 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172708 | TTTCTGAAGTTGTTG[A/G]AAAAAAGAATCAGAA | 9690 |
rs762791362 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254152 | ATTCAGGTACCCTAC[C/G]TGCTGACTTTCTGGG | 9690 |
rs762796703 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209289 | ATTAGCAGCAGCAGC[C/T]GTAACTGATAATGTT | 9690 |
rs762837792 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160535 | TTTGGCAAGACTAAC[A/G]CAATAGTTGATTGTA | 9690 |
rs762838876 | snp | C/G | 3.30918e-05 | 0.00406753 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182163 | GCACCTTTTACAGAT[C/G]AGATTTTTCATTTCA | 9690 |
rs762838890 | snp | C/T | 6.59359e-05 | 0.00574139 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207409 | CAAGGTCTATGGTAC[C/T]GTTGCTTCAGGTGAT | 9690 |
rs762847788 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260495 | CTGTGTGGTGGCAGA[G/T]TCTGGAGGGCTTGCT | 9690 |
rs762865776 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197793 | AATCTTTGTATCAAA[C/T]GACTCCCATCTGCTA | 9690 |
rs762890583 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159638 | TTTGGGAGGCTGAGA[C/T]GGGTGGATCACTTGA | 9690 |
rs762907276 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247311 | AACAAGATAATTAAT[A/G]TCTAACTGCATGTCT | 9690 |
rs762922341 | snp | G/T | 1.72311e-05 | 0.00293518 | intron-variant | UBE3C | GRCh38.p7 | 7:157178673 | TAAGTGTGTGAATAC[G/T]TTTTTCATTTTTACA | 9690 |
rs762937740 | snp | A/G | 3.3006e-05 | 0.00406226 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220738 | TGTGGAGGTTCCGGC[A/G]GATGGGGAGGATAGG | 9690 |
rs762945964 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245728 | GGGATGTTATGCCGG[C/T]TCTAGTTATCAGACA | 9690 |
rs762951891 | snp | A/T | 1.73595e-05 | 0.00294609 | intron-variant | UBE3C | GRCh38.p7 | 7:157223388 | TTGTCACTACGTATC[A/T]TATTAGTGTTAAGAA | 9690 |
rs762954834 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198231 | CAAAAGGAATTACCC[A/G]ATCTGTATCCTCCAC | 9690 |
rs762956213 | snp | A/G | 3.31203e-05 | 0.00406928 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170391 | AATGGCCCCAACCTT[A/G]CCCTTTTGGTAAGGC | 9690 |
rs762966547 | in-del | -/CTAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188769 | GCAAGTAGGCTTACT[-/CTAA]CTAACTGTTACAGAT | 9690 |
rs763028498 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163926 | CATTTAAACATGCCT[A/T]GGTTTTACTGTATAT | 9690 |
rs763037879 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180170 | TTTCTAACAGTCGAT[A/G]AAATTTTAGCCTTTT | 9690 |
rs763039787 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247463 | CTGGGAGGCCGAAGT[A/G]GGTGGATCACCTGAG | 9690 |
rs763042787 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263274 | TTCCCAGGCACCTGT[C/T]GTAACGCCACCTTCC | 9690 |
rs763050282 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148684 | AACTTTTTCTTACAG[A/G]TCTGGCATCAAATAA | 9690 |
rs763069733 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201561 | GTGTCTCATCAAATG[A/G]CTGGTTGTCTGAGGC | 9690 |
rs763075068 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230139 | GTCTCGAACTCCTGA[C/T]CTCAAGGCGATCCGC | 9690 |
rs763146335 | in-del | -/TT | 1.64827e-05 | 0.00287073 | intron-variant | UBE3C | GRCh38.p7 | 7:157201825 | ATGTATTATACAGAC[-/TT]ATAAATTGAGCTCAA | 9690 |
rs763154064 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175429 | TAGAATACACCTTTC[A/G]TCAGGCTTTTTATTA | 9690 |
rs763195020 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248515 | TTTCTGAAGAGCTAC[A/G]AAGACGATGTGGAGG | 9690 |
rs763208042 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231830 | CAGGTCTTCTGTTAT[A/G]AGCAGTCAAAACGGA | 9690 |
rs763276134 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228124 | TAGTCATTGAAGTGA[A/T]TCCATGCTTTACGAT | 9690 |
rs763281516 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258380 | AACCTGGGCAATGTA[C/G]TAGCGAGATCCTGTC | 9690 |
rs763281738 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238463 | CATCATATTCAAGGA[A/G]ATTTGCTGATGAATG | 9690 |
rs763282606 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264650 | GCAATGCGTGATCTC[A/G]TCTCACTGCAGCCTG | 9690 |
rs763297606 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222221 | TTATAAAGCTATTCT[A/C/G]GATATAGTTTATCAG | 9690 |
rs763301031 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144706 | AAAAAAAAATAGACT[G/T]TATTTTTTAGAGCAG | 9690 |
rs763305227 | in-del | -/C | 1.65704e-05 | 0.00287836 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225520 | TGAAGATGCTTATGA[-/C]AAACTTTCTCCAGAA | 9690 |
rs763365432 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231083 | TTTTTTTAACAGAGC[C/G]TGATTTGAAAAAGCG | 9690 |
rs763370521 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193253 | TTTTATGGCATTAGA[A/G]GTGTCCAGTAATATT | 9690 |
rs763383380 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257458 | CTGGAAATTAATGTT[C/G]ATCTTACGTAATTTG | 9690 |
rs763383506 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156661 | TTTACACATCCTGTC[A/G]GAGCTGTTCTCTACA | 9690 |
rs763389092 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209606 | ATTTGATTAAACCCT[-/G]GGGTCTTTGTTAATA | 9690 |
rs763392856 | snp | C/T | 2.01941e-05 | 0.00317752 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186967 | TCTTCACCACCATGG[C/T]CTCCGTCTGCCACAC | 9690 |
rs763399370 | snp | A/G | 5.62319e-05 | 0.00530215 | intron-variant | UBE3C | GRCh38.p7 | 7:157139348 | AGGAAGGTGAGGGCC[A/G]GGCTGGCGGGGCGCC | 9690 |
rs763445359 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233210 | CATGTTTTCAGGTTT[C/T]ATTCATGTCGTAGTA | 9690 |
rs763464597 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211538 | GAGGTTGCGAATTTT[G/T]TGTGTGAAAAATCAG | 9690 |
rs763470377 | snp | C/T | 1.74066e-05 | 0.00295008 | intron-variant | UBE3C | GRCh38.p7 | 7:157223389 | TGTCACTACGTATCA[C/T]ATTAGTGTTAAGAAA | 9690 |
rs763489657 | snp | A/T | 1.65457e-05 | 0.00287621 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178842 | TGCACTACATGATTC[A/T]CAATGGTAAGTAGTA | 9690 |
rs763515066 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250574 | GTGATCCTCCTGCCT[A/C]AGCCTCCCAAAGTGC | 9690 |
rs763531361 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222989 | GCTGTGCACTTGAGA[C/T]GTGCTAGACAGCTGG | 9690 |
rs763537058 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246599 | TAAAGAGGGTCTGGG[C/T]CTATCACAGCATCTC | 9690 |
rs763543088 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209945 | CAGCACTTTGGGAGG[A/C]CAAGGCGGGTGGATC | 9690 |
rs763545991 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163517 | GACATTGGTACGGAG[C/T]ACCAGTCTTACTCAA | 9690 |
rs763571954 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145784 | TTTAGAGTGGTTTAC[A/G]GTTTACAGAATAATT | 9690 |
rs763579700 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178113 | TCGGGAGTGGCAGAT[A/G]TGCTCTGTGTCTTGA | 9690 |
rs763585423 | in-del | -/TCC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156132 | CAGTGGTGAACTTGT[-/TCC]TCATTATATTGAGCT | 9690 |
rs763588759 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216645 | AAAATTATCATGTAC[A/G]TGTGTTTGTGTTGTT | 9690 |
rs763595747 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232148 | TCCAACATTGCCTTA[-/T]TTTTTTTTAATAAGG | 9690 |
rs763607729 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184923 | ATGGCTGAGGGGTGG[A/G]CTGATGACAAAGGAG | 9690 |
rs763608477 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230878 | TGCAGTGAGCCGAGA[G/T]CGTGCCACTGCACTC | 9690 |
rs763618338 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253830 | CTCGGGTACTATTTC[A/G]TATTTAGATTCTTGT | 9690 |
rs763630444 | snp | A/T | 1.6784e-05 | 0.00289685 | intron-variant | UBE3C | GRCh38.p7 | 7:157201690 | AAGTAATTGCTTTAC[A/T]GTTCTGTGTTTTTCT | 9690 |
rs763659098 | snp | G/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137916 | AATTTTGCTAAGAGA[G/T]TAGATTTTATGTACT | 9690 |
rs763664474 | snp | G/T | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157175031 | TGATGAGCCTCTGTT[G/T]CAGGTAAAATTCTAT | 9690 |
rs763713771 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167531 | ATATAAAATGCCTCT[C/G]TCTCTCTCTTTTCTT | 9690 |
rs763754352 | snp | G/T | 0.0116636 | 0.0754704 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174928 | TTTCAGATATGGCTG[G/T]ATCAGAACTTAATTA | 9690 |
rs763796682 | snp | C/G | 1.68083e-05 | 0.00289894 | intron-variant | UBE3C | GRCh38.p7 | 7:157254322 | TCAGGTATGTTATCA[C/G]TGCTAGTTATTGTTT | 9690 |
rs763817343 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259764 | GGAGCGACCCAAAAC[C/T]GGATTGTGGGGGTCG | 9690 |
rs763824304 | snp | C/T | 1.65414e-05 | 0.00287583 | intron-variant | UBE3C | GRCh38.p7 | 7:157184047 | AAGCCCCGTGCCCTG[C/T]ATCTGGGGGGCTGCG | 9690 |
rs763853954 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159643 | GAGGCTGAGACGGGT[C/G]GATCACTTGAGGTCA | 9690 |
rs763883706 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158668 | GAAGACAAACTTGGT[C/T]CTGTTCACTAGAGAC | 9690 |
rs763904149 | snp | A/G | 1.66413e-05 | 0.0028845 | intron-variant | UBE3C | GRCh38.p7 | 7:157169155 | TGAGGAGATTAGTAG[A/G]GCATGGGAGAGCTTA | 9690 |
rs763915536 | in-del | -/CT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142141 | AATTATGTTGAGCAC[-/CT]CTACATATGCTTGTT | 9690 |
rs763917986 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246159 | AATGTGAATCTCAAG[C/G]GGTGTCTGAGCATGC | 9690 |
rs763937152 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182270 | TAGATGTTCAAGAAA[A/G]AGTGGTGGAGCACCC | 9690 |
rs763977122 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225537 | AACTTTCTCCAGAAA[A/G]TGGTATATATAATTC | 9690 |
rs764015522 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162344 | GGACTACTGGTATGT[A/G]CCACCATGCCCGGCT | 9690 |
rs764021203 | snp | C/G | 1.65351e-05 | 0.00287528 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182165 | ACCTTTTACAGATCA[C/G]ATTTTTCATTTCATC | 9690 |
rs764033213 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198292 | GCTCTTGAAGACTGC[A/T]GCTTTAGGTCTGTCA | 9690 |
rs764065036 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226338 | ACTGGCACGTTTCGT[C/T]GTATGTTCATATTTG | 9690 |
rs764066970 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215746 | TGATCCAATCCTGGT[A/T]GTAGACATTTAAAAT | 9690 |
rs764070732 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241937 | ATGGTTCCATTTATA[-/T]GAAATGTCCAAAACA | 9690 |
rs764088203 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173197 | GGCCAAAATACCAGA[-/C]CCCCACCTGTAAAAC | 9690 |
rs764126188 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187638 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 9690 |
rs764130455 | snp | C/T | 0.000263822 | 0.0114822 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186860 | ACTGTCAGTATCATA[C/T]ATAACAGAGGAATGC | 9690 |
rs764136665 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151602 | CCTGCATTATCCTGC[C/T]GGAAATACTATCTAT | 9690 |
rs764208590 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190002 | GATGGGGTTTCACCA[C/T]GTAGGCCAGGCTGGT | 9690 |
rs764215029 | snp | A/G | 9.90099e-05 | 0.00703528 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220739 | GTGGAGGTTCCGGCG[A/G]ATGGGGAGGATAGGC | 9690 |
rs764226837 | snp | C/G | 1.7174e-05 | 0.00293031 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170322 | TCCATCCAAAGAAGT[C/G]CATTTGATCGCTGTG | 9690 |
rs764233452 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212599 | CTTGAACAGTTGTCA[A/C]GTGTGATTTTTATAA | 9690 |
rs764248589 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157136966 | GGAGTCTCCCTCTGT[C/T]CCCCAGGCTGGAGTG | 9690 |
rs764254492 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263292 | AACGCCACCTTCCCC[A/G]GGCGCCTGTCCTAAC | 9690 |
rs764254787 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191179 | TTAATTATGTCTTGT[C/G]TTGTTAATCATTGTG | 9690 |
rs764269960 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140821 | TCAGAATCTCAAGGG[A/T]AGATAGCACGAGCTG | 9690 |
rs764270054 | snp | A/G | 3.00621e-05 | 0.00387687 | intron-variant | UBE3C | GRCh38.p7 | 7:157217009 | ATATTTATCATTAAA[A/G]AATACATTCAGCTTG | 9690 |
rs764293723 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163950 | TGTATATATGTATGT[C/G]TGTATGTATTTTTTA | 9690 |
rs764298149 | snp | A/G | 1.67877e-05 | 0.00289716 | intron-variant | UBE3C | GRCh38.p7 | 7:157207664 | TGTGTGTTAAAAGAT[A/G]GAAAAAGAAACAATA | 9690 |
rs764317312 | in-del | -/T | 1.65979e-05 | 0.00288074 | intron-variant | UBE3C | GRCh38.p7 | 7:157207694 | GAAAACTGGATTGTG[-/T]TTTTTTAGTTGTAGG | 9690 |
rs764333285 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190670 | CTGACTTGTGGAAAA[C/T]ACAACCCTGATTATT | 9690 |
rs764375010 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228137 | GAATCCATGCTTTAC[A/G]ATGCTCGTTGTCTTA | 9690 |
rs764379994 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231096 | GCCTGATTTGAAAAA[A/G]CGGATCCGTGTGCAC | 9690 |
rs764384347 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157256478 | TTGCTCTCCCCTTCT[C/T]GTACTTTGCCCATCG | 9690 |
rs764410003 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179648 | TAAAAATGTGCGTGA[A/G]ACTAGTTGTGAAGGG | 9690 |
rs764433080 | snp | A/C/G | 3.3004e-05 | 0.00406216 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181561 | TAACAGCAAGCTTCC[A/C/G]TCAAGTATTGAATAT | 9690 |
rs764439186 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223006 | TGCTAGACAGCTGGA[A/G]TGGAAGTGTAGTCCT | 9690 |
rs764478269 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145794 | TTTACGGTTTACAGA[A/G]TAATTGATGGGAAAC | 9690 |
rs764484018 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246693 | CTCTGTCCTTCCTGC[C/T]GTCCCTCATTCTCGG | 9690 |
rs764503665 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156479 | CCCGGCTAATTTTTG[-/T]TATTTTTCATAGAGA | 9690 |
rs764508104 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194821 | TGTAAAGCAGAATTT[A/T]TAAGTGATGACTTCA | 9690 |
rs764529274 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212547 | CTCAAACATAGCGAT[A/C]TTGTGAAAACAGTGC | 9690 |
rs764534367 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | UBE3C | GRCh38.p7 | 7:157163803 | TTTTTTCTCTGTTTG[A/G]GTGTAGGAGGAAAAG | 9690 |
rs764596005 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211602 | ATCCCACAAGCTTAG[C/T]GTTCCAGTAATGGAA | 9690 |
rs764597690 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172987 | AACATATTTGACTTT[C/T]GGCCTCGAGCAAATA | 9690 |
rs764604590 | snp | C/T | 1.6596e-05 | 0.00288058 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254292 | CTAGAGGACCTAAAA[C/T]CCTTTACAAACTATT | 9690 |
rs764622261 | snp | A/G | 1.73222e-05 | 0.00294292 | intron-variant | UBE3C | GRCh38.p7 | 7:157139350 | GAAGGTGAGGGCCGG[A/G]CTGGCGGGGCGCCCT | 9690 |
rs764676765 | snp | A/T | 3.31087e-05 | 0.00406857 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178844 | CACTACATGATTCAC[A/T]ATGGTAAGTAGTAGG | 9690 |
rs764680507 | snp | A/G | 6.60862e-05 | 0.00574793 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174921 | TTTGCTGTTTCAGAT[A/G]TGGCTGTATCAGAAC | 9690 |
rs764695567 | snp | C/T | 1.6722e-05 | 0.00289149 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267724 | AACTTCTCTATGCGA[C/T]TGAATGTGCCGCTGG | 9690 |
rs764695973 | in-del | -/GTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232352 | CAGGAATTGTTATTA[-/GTTT]GTTTGTTTGTTTGTT | 9690 |
rs764699433 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170240 | AGCAACGTATATTTA[C/T]ATCATAAGAATTGTG | 9690 |
rs764708341 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267775 | GATGCTGGGGTCAGA[C/T]CCCTACAGAGAACCA | 9690 |
rs764715139 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186499 | AAATGCCATTAGATG[A/G]TGATAGTTTCACTAT | 9690 |
rs764720355 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173881 | AAATTAACTAATATT[C/T]GGAGTAGTTCAGAAT | 9690 |
rs764746954 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267597 | CAGGAGTTGTATCCC[A/G]CATTTTGTATTCACA | 9690 |
rs764768333 | in-del | -/TTGTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167770 | CTCGATCTCCTGACC[-/TTGTG]ATCCTCCTGCCTCGG | 9690 |
rs764797735 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147352 | ATTTGTAGAGAAGCA[A/G]TTGACTTTCATGTAC | 9690 |
rs764802012 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159500 | GTTTCTTGAAGCAAA[A/G]GTTTGTTAAAGCAAA | 9690 |
rs764847217 | snp | C/T | 1.65228e-05 | 0.00287422 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254106 | CAATGTCGTCAGCCT[C/T]GAGTGGCTCCGAATG | 9690 |
rs764851187 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148162 | AGTGCCTGGAGTACA[C/G]TGGTGCGATCTCACT | 9690 |
rs764869657 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248170 | GTTCTCTGCATGCTT[A/G]GTGCGTGCATTGAAT | 9690 |
rs764884134 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180606 | GTATATGATGAGATA[C/T]TCAAAAATTGCACCT | 9690 |
rs764929826 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207778 | CTCGATGCCTTCGAG[A/G]TGCATGCCTGGGGAT | 9690 |
rs764954116 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237257 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 9690 |
rs764956760 | in-del | -/TC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260449 | GACCAGATAGGAGAA[-/TC]TCTCGAGCGCAGGGA | 9690 |
rs764961006 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141482 | TGCACACCTAGCTGC[C/T]TGGTACAGCCCGTTG | 9690 |
rs764961377 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249048 | AAAAGAAAGGTCTAT[A/G]TTAGAGATTCAAACT | 9690 |
rs764963269 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264463 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACC | 9690 |
rs764964049 | in-del | -/AAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267432 | ATCTCAAAGAAAACA[-/AAC]AACAACAACAAAGCA | 9690 |
rs765004539 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204288 | TTGCTAGGACTTACA[A/G]CTTTAGTGGGCAGAA | 9690 |
rs765008042 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240040 | ACCTTCTGAATCTGG[A/G]ACTCTAGGGCTAGGG | 9690 |
rs765011743 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170752 | CTGACACAGCCTTAG[C/T]AGTTGCCAGCACGCC | 9690 |
rs765026502 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169519 | TAGCTGGGATTACAG[G/T]CATGTGCCACCACGT | 9690 |
rs765040531 | snp | C/T | 1.65526e-05 | 0.00287681 | intron-variant | UBE3C | GRCh38.p7 | 7:157181697 | AATGGATTTATTGAT[C/T]TTGTCCTTTCACAAG | 9690 |
rs765043223 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150379 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAGAGT | 9690 |
rs765084127 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201777 | ATCTTTGGTTTCTAA[C/T]ATCTTCCATGTCAAC | 9690 |
rs765128284 | snp | A/G | 1.72033e-05 | 0.0029328 | intron-variant | UBE3C | GRCh38.p7 | 7:157201675 | AGAAATGTTTTGAAT[A/G]AGTAATTGCTTTACT | 9690 |
rs765162206 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185295 | GCTCTCACTCGTGCT[C/G]ACACTTTGAACATTT | 9690 |
rs765169345 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247788 | CTCATTGACACATTG[G/T]CCATGGCTGCTTTTG | 9690 |
rs765181124 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144640 | TTTGTAGATCTGACA[A/G]TAGTGGGAGTAGAAT | 9690 |
rs765208843 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209212 | ATCCTCCAAGTCCAC[A/G]AGAGTCTCTCTCCAG | 9690 |
rs765224822 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197692 | TATTCGGAAATGAAG[G/T]CACAAGAATAAAGTC | 9690 |
rs765247379 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158368 | TGAAACCGTAAGCCA[C/T]AGCACCCAAAACCTG | 9690 |
rs765248611 | snp | C/T | 1.84841e-05 | 0.00304002 | intron-variant | UBE3C | GRCh38.p7 | 7:157216830 | CATTGTGCTGCCGAG[C/T]TCACGTGTGTGACGC | 9690 |
rs765261144 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224298 | CTCCCGGATTCAAGC[A/G]ATTCTCCTGCTTCAG | 9690 |
rs765322565 | snp | A/T | 2.51702e-05 | 0.00354746 | intron-variant | UBE3C | GRCh38.p7 | 7:157216999 | GATCTTTTTAATATT[A/T]ATCATTAAAAAATAC | 9690 |
rs765339316 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant | UBE3C | GRCh38.p7 | 7:157184058 | CCTGCATCTGGGGGG[C/T]TGCGATGCAGGCAGC | 9690 |
rs765373612 | snp | G/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248484 | CCTAGACCCTGAGGT[G/T]TATAAGAATTTGCTC | 9690 |
rs765382803 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193761 | CTGACCTCACACATG[G/T]TTGTCTGTTCATTGT | 9690 |
rs765389747 | snp | A/T | 3.32193e-05 | 0.00407536 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182153 | GTTTCTGGCAGCACC[A/T]TTTACAGATCAGATT | 9690 |
rs765392440 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173318 | GTATTCAAGGCTGCA[G/T]TGAGCTATGATCCTG | 9690 |
rs765420625 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236391 | TGGGATGGCATGCCT[A/G]TAAATCAGATTATTT | 9690 |
rs765426112 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162206 | ATTTAATTTTTTTTT[C/G]TTTTTTGAGACGGAG | 9690 |
rs765428360 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173833 | GTGGGCAAGGTGGCT[C/G]CAAACACCTCAAGAG | 9690 |
rs765439508 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263236 | TAACACCACCTTCCC[C/T]GGGCACCTGTCCTAA | 9690 |
rs765467211 | snp | C/T | 6.02537e-05 | 0.00548846 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139225 | CGTGCCCCGCCCGCC[C/T]GGCTGCTTCCGCGGC | 9690 |
rs765488178 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179297 | AATTTTGTTAAATGA[-/T]TTTTCTTCCAAGAGT | 9690 |
rs765500637 | in-del | -/T | 4.40228e-05 | 0.00469142 | intron-variant | UBE3C | GRCh38.p7 | 7:157188907 | CTTTTATTTTCAGAG[-/T]TAGGATTTGCCATTT | 9690 |
rs765522264 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166422 | ATTTTTCAGAATTCC[C/G]TTGTATCTCACTGAG | 9690 |
rs765527662 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | UBE3C | GRCh38.p7 | 7:157267574 | CATCTTGCACACATG[C/T]TGTTTTTCAGGAGTT | 9690 |
rs765545818 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185490 | GGGTATTGTCCACAT[G/T]TGGGCTGAGAACTAA | 9690 |
rs765592986 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205188 | AGAGACCTGTGTCTC[A/G]TTTGTGCCCTGTCTG | 9690 |
rs765624737 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266939 | TGGAAATGAGGTCTC[A/G]TTATGTTGCCCAGGC | 9690 |
rs765647551 | snp | A/G | 0.00011568 | 0.0076044 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178833 | AACAAATTTTGCACT[A/G]CATGATTCACAATGG | 9690 |
rs765666332 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205366 | CCCAATATAAGAATT[C/T]TATGCATCCTGCAAT | 9690 |
rs765690674 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191768 | GCAGAAAAATACAGA[G/T]TTGTTTTTCATTGTA | 9690 |
rs765732384 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244971 | TGCATAAAAAATAGG[C/T]AGTTTTTGAAGTTGT | 9690 |
rs765735828 | snp | A/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178736 | AATGTTGCACTTCCA[A/G]TGAGAATGCTTGAAG | 9690 |
rs765743921 | in-del | -/GTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232355 | AATTGTTATTAGTTT[-/GTTT]GTTTGTTTGTTTGTT | 9690 |
rs765763147 | snp | A/T | 3.47041e-05 | 0.00416544 | intron-variant | UBE3C | GRCh38.p7 | 7:157182375 | ACACATATGGGTAGC[A/T]TTGGCAGATGAGTCA | 9690 |
rs765772219 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230083 | CTGGCTAGTTTTTAT[A/G]TTTTTAGTAGGGATG | 9690 |
rs765786298 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222171 | CCACTGCACACTGCC[C/T]GTGAACATGTTTTTT | 9690 |
rs765820654 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234200 | AATTTTGAAGTCTAA[C/T]GTGTTTTTTTCTTTT | 9690 |
rs765820921 | in-del | -/TA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229035 | ATATGTTTGGGTGAC[-/TA]TGCACCAAAGCCAAC | 9690 |
rs765825320 | snp | C/G | 1.65515e-05 | 0.00287671 | intron-variant | UBE3C | GRCh38.p7 | 7:157186822 | GAGACTGGTTGTTCT[C/G]GTATGTTCTAGGAGG | 9690 |
rs765866564 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196225 | TTCTCCTATGCAACG[A/C]TGCCGACAAACTGAT | 9690 |
rs765867457 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158190 | AGCCACTGTGCCTGG[C/T]CCTAGAGTCAGCTTT | 9690 |
rs765910374 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224257 | TGGAGTGCAGAGGCG[C/T]GATCTTGGCTCACTG | 9690 |
rs765912098 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147221 | TCATTGGTTATATAA[C/T]TTTCCTTATATATAC | 9690 |
rs765919507 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185225 | CCTCGCTGTGGGTGT[G/T]CAAACACGATGAAAG | 9690 |
rs765919784 | snp | A/G | 6.64706e-05 | 0.00576462 | intron-variant | UBE3C | GRCh38.p7 | 7:157207595 | GCTGCTGGCCACTTG[A/G]CCCATCAGTTTTCAT | 9690 |
rs765959283 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182298 | CCCTGGCTTTTCTAT[C/T]TCGTTTTAACTGTTG | 9690 |
rs765973934 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146223 | TGTCAAAGATCAGTT[A/G]GCTATATTTTTATGG | 9690 |
rs765977513 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175220 | TCAGGCCGGCATGAG[A/G]TATAAATGAAGACAC | 9690 |
rs765988792 | snp | G/T | 1.65048e-05 | 0.00287265 | intron-variant | UBE3C | GRCh38.p7 | 7:157231072 | ACCCTCCCATTTTTT[G/T]TTAACAGAGCCTGAT | 9690 |
rs766011705 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169860 | TAAATGTTTTTGTAT[C/T]TTTAGTAGAGATGGC | 9690 |
rs766019798 | in-del | -/TGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166913 | GTCGCTTTTTCCTGT[-/TGG]TGGTGGTGGTGGTGG | 9690 |
rs766038966 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137628 | GGAGTGCAATAACAC[A/G]ATCTCAGCTCACTGC | 9690 |
rs766051266 | snp | A/T | 1.65512e-05 | 0.00287669 | intron-variant | UBE3C | GRCh38.p7 | 7:157223231 | TACAAGTGAACTAAT[A/T]AAGGTTTTAAAATGT | 9690 |
rs766059308 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212991 | TTGAACTCCTAGGCT[C/T]GAGTGATCTGCCTGC | 9690 |
rs766108143 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259439 | CAACATATTTTCACA[C/T]AGTGTGTTTATGAAT | 9690 |
rs766117930 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151376 | AGCATTGTCAACATA[C/T]ATTTTGGTGAATGTG | 9690 |
rs766123647 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247982 | TCATGTGGTTTTCAG[C/T]CTCGCAGTGTGTGAT | 9690 |
rs766127422 | snp | C/T | 4.37092e-05 | 0.00467468 | intron-variant | UBE3C | GRCh38.p7 | 7:157188917 | CAGAGTTAGGATTTG[C/T]CATTTAATTTCTGTT | 9690 |
rs766166104 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206653 | GAGTGCAGTGGCGCA[A/G]TCTCAGCTCATGGCA | 9690 |
rs766168442 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241051 | TTAGCGGGAGGGAAG[A/G]GAAGGATGGTCTGGA | 9690 |
rs766186724 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214098 | TCCTTTCCTCCTCCT[C/T]TCTCCCCATCTCCCT | 9690 |
rs766192267 | snp | C/T | 1.66167e-05 | 0.00288237 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220775 | GCAGTCCACCCTGGA[C/T]GGTGAGTTCTCTAGG | 9690 |
rs766206321 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213076 | TGTGCATTTCTGAAT[A/G]AATTTATTAGTACTT | 9690 |
rs766213791 | snp | C/T | 0.000226526 | 0.0106401 | intron-variant | UBE3C | GRCh38.p7 | 7:157223130 | GCGGGGATGTGTTCA[C/T]GGAACTGGATTTAGA | 9690 |
rs766237206 | snp | A/C/T | 5.00808e-05 | 0.00500383 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170421 | CAGCTTCTGTTTTTT[A/C/T]ACAAACAAAATGAAG | 9690 |
rs766257194 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241783 | ATCAGCTGACAAACG[C/G]GTAAACAGAATACGG | 9690 |
rs766260170 | snp | C/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178446 | TTCTCCACTGTCCAT[C/G/T]TTTCTTGTCTGTGAA | 9690 |
rs766260700 | snp | A/T | 3.40779e-05 | 0.00412769 | intron-variant | UBE3C | GRCh38.p7 | 7:157174883 | AACTATTAAATTTTC[A/T]TTGAGAGTTGTATAT | 9690 |
rs766312755 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195418 | TGAAAAAGTAAAGAT[A/G]ATTGAGACAGTCACA | 9690 |
rs766313767 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167712 | CGGCTAATTTTTTGT[A/G]TTTTTAGAAGAGGTA | 9690 |
rs766331360 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230552 | ATAGAAAAATTAGCC[A/G]GGTGTGGTGGCACAC | 9690 |
rs766332207 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141363 | CACCCATTCATTACA[A/G]TCATATGTGACTTAA | 9690 |
rs766340662 | in-del | -/T | 0.0024023 | 0.0345742 | intron-variant | UBE3C | GRCh38.p7 | 7:157231066 | CTCCTCACCCTCCCA[-/T]TTTTTTTTAACAGAG | 9690 |
rs766351987 | snp | C/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182224 | TTTTCCCTTACGAGC[C/T]CTTTCTGAATGCACT | 9690 |
rs766365202 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208155 | TCATACTCCACTGCA[A/G]CCTTGAACTCCTGGG | 9690 |
rs766380512 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231285 | GCTTGTGGGAGATTC[C/T]TTTGCCAGACATTAC | 9690 |
rs766417586 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268614 | TTGTCCCGATGCTAG[C/T]CGTGCCGGTCTCCCA | 9690 |
rs766417948 | snp | A/G | 3.30131e-05 | 0.00406269 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254092 | CGCCAGGGCCTTGCC[A/G]ATGTCGTCAGCCTCG | 9690 |
rs766439261 | in-del | -/AATACACTAACAGTAGCTGATAAGCTTTTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230366 | TTGGGCCACAGACAA[lengthTooLong]AAAAAAAAAAAAAAT | 9690 |
rs766439396 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221097 | CTGTGTGGGTTGATT[A/G]TTCCCTCTGTTGCTC | 9690 |
rs766482616 | snp | A/G | 1.65231e-05 | 0.00287424 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181669 | CTGTCCGGAAGGTGC[A/G]AGGTGAGACTGGAAT | 9690 |
rs766493499 | snp | C/G | 3.76825e-05 | 0.00434049 | intron-variant | UBE3C | GRCh38.p7 | 7:157189009 | ATTTCCGAGACAGAT[C/G]CGTACATGAAAACCG | 9690 |
rs766520436 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183268 | GAGGCCGATTACAAG[G/T]AGTAGGTTGTCACCT | 9690 |
rs766531174 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154733 | TGATTGCGTTTTGCA[G/T]TGGATACTTCATTTT | 9690 |
rs766561470 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210138 | GCCGAGATAGCGCCA[C/G]TGCACTCCAGCCTGG | 9690 |
rs766565908 | snp | A/G | 1.68969e-05 | 0.00290657 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207893 | CTCTGAAATGCAACA[A/G]TGCATACAGATGGAA | 9690 |
rs766570796 | snp | A/C | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181585 | TGAATATTCTGATTT[A/C]TCTCGAGTTCCTATA | 9690 |
rs766582538 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143253 | ATGATGCAGTTTAAT[G/T]GGGGGTATGTTTTTC | 9690 |
rs766593487 | in-del | -/ACAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264297 | CATGCTTGGCCTGTT[-/ACAC]ACACACACACACACA | 9690 |
rs766593494 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164526 | CTTAACTGTTTGTGA[A/G]GAAGGTAAAAGAAAG | 9690 |
rs766609345 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159814 | GGCCAGAGCGAGACT[C/G]TGTCTCCAAAAAAAT | 9690 |
rs766610071 | snp | A/G | 3.36106e-05 | 0.00409929 | intron-variant | UBE3C | GRCh38.p7 | 7:157175056 | TTCTATTGTAAGTCA[A/G]TAACGTATATAATGT | 9690 |
rs766659605 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225708 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGTGAGA | 9690 |
rs766677049 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256962 | TCTTCTGGAGAGTTG[C/T]GGAAGGGTTCACTGA | 9690 |
rs766690865 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234573 | GGATATAGAATAATT[-/C]CCCTTTATTTGTGTC | 9690 |
rs766720616 | in-del | -/T | 1.79297e-05 | 0.00299408 | intron-variant | UBE3C | GRCh38.p7 | 7:157170281 | TATATTTATGGGTCA[-/T]TTTTGTTTTGTTTTT | 9690 |
rs766742651 | in-del | -/TGTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187560 | CTAATTTTTTGTTTT[-/TGTG]TGTGTGTGTGTTTGT | 9690 |
rs766769041 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258406 | CTGTCTCAAGGGGGA[A/G]AAAGTAATGTTAAGG | 9690 |
rs766805227 | snp | C/T | 0.000149672 | 0.00864948 | intron-variant | UBE3C | GRCh38.p7 | 7:157186786 | GTAGTGTAGAGGACG[C/T]TCCAGTTGAGCACAT | 9690 |
rs766871215 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, intron-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157169077 | GTTGAAAAATGCAAT[A/G]ATTATCCAGTCATTT | 9690 |
rs766883977 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189605 | CCTGCGGTGCCCACT[C/G]AGCCCCGCGGCATTC | 9690 |
rs766896010 | snp | C/G | 1.65594e-05 | 0.0028774 | intron-variant | UBE3C | GRCh38.p7 | 7:157184052 | CCGTGCCCTGCATCT[C/G]GGGGGCTGCGATGCA | 9690 |
rs766901304 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207441 | TCCAGGGGTTCTCCT[A/C]TGTCTTTTGAAGATT | 9690 |
rs766913597 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160733 | TTTCTCCTCAAACTT[C/T]TGCCCACTAATTTTA | 9690 |
rs766952310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241645 | CTTTGGAAAAGTTTA[A/G]CAGTTCCTCAAAAGG | 9690 |
rs766979248 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206379 | GTGATTCCCCTGCCT[C/T]AGCCTCCCAAGTAGC | 9690 |
rs766988991 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195288 | GACCCACAAGTTTCT[C/T]GACAATGTTATAGCA | 9690 |
rs767001351 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168715 | ATATTGTATGATTCC[A/G]TTATATGAAGTGTCC | 9690 |
rs767031321 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184453 | ACTTTCAAGTTCTTA[C/T]CTCTTTTCTTCCTTA | 9690 |
rs767042439 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257694 | GTGAGCCGAGATCGC[A/G]CCACTGCACTGCACT | 9690 |
rs767055513 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254749 | AATGTACATGGTTCA[A/G]AAACCAGATGGCTGA | 9690 |
rs767067458 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225443 | GCAGATAAGCAAGAA[A/G]TTCAAGGAGATGGTC | 9690 |
rs767070742 | in-del | -/ATAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157974 | AACAGATATATATAG[-/ATAT]ATATATATATAGAGA | 9690 |
rs767109840 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184157 | TTTGCAGAGAAGCCC[C/T]GTCAGCCCCACTACC | 9690 |
rs767122475 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | UBE3C | GRCh38.p7 | 7:157267569 | AGTGACATCTTGCAC[A/T]CATGCTGTTTTTCAG | 9690 |
rs767122623 | snp | C/T | 1.65666e-05 | 0.00287802 | intron-variant | UBE3C | GRCh38.p7 | 7:157225358 | TTCTTTGGTAGGTTG[C/T]AAGAGGTCTTTTGTT | 9690 |
rs767168473 | snp | G/T | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269859 | TTTACAGGATGGTGT[G/T]TGCTTTTGCGGAGTG | 9690 |
rs767190992 | in-del | -/AGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222306 | TAGCAGTGTCTTTCA[-/AGG]AGGAGAAGTTTTAAA | 9690 |
rs767209286 | snp | C/T | 6.74104e-05 | 0.00580523 | intron-variant | UBE3C | GRCh38.p7 | 7:157178687 | CTTTTTTCATTTTTA[C/T]AGGTTGCTGCAAAAC | 9690 |
rs767212216 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246751 | ACAGTAGGAAGGCCC[A/G]TGACTGCCTCTGTTG | 9690 |
rs767235357 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222441 | TCTTTCTTTTTTGAG[G/T]CAGGGTCTCAGTGTG | 9690 |
rs767235407 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233359 | GCACTGCTACAAACA[C/T]GGCTCAGTCCTGCGC | 9690 |
rs767242609 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217230 | ATTAAAGCCTTAATG[A/G]TTCTTTGTGAGGTTG | 9690 |
rs767251674 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261322 | GAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]AAAAATCCCAAATAG | 9690 |
rs767257348 | snp | C/T | 1.65315e-05 | 0.00287498 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220756 | TGGGGAGGATAGGCC[C/T]GCTGCAGTCCACCCT | 9690 |
rs767277188 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150062 | CACAACCTACCTAGG[A/G]TTGGTTATAACAGAT | 9690 |
rs767323282 | snp | A/G | 0.000267473 | 0.0115613 | intron-variant | UBE3C | GRCh38.p7 | 7:157223162 | AAATGAGTTAATCAG[A/G]ATGATTTCAAGAATC | 9690 |
rs767351069 | snp | C/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248538 | TGTGGAGGAGCTTGG[C/G]CTGAACTTCACTGTG | 9690 |
rs767354440 | snp | A/G | 3.6135e-05 | 0.00425043 | intron-variant | UBE3C | GRCh38.p7 | 7:157253922 | TTATCATACTTTGAG[A/G]ATTTTGAGATCCTTA | 9690 |
rs767370362 | snp | A/G | 1.65985e-05 | 0.00288079 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170408 | CCTTTTGGTAAGGCA[A/G]CTTCTGTTTTTTTAC | 9690 |
rs767373096 | snp | A/C | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182281 | GAAAGAGTGGTGGAG[A/C]ACCCTGGCTTTTCTA | 9690 |
rs767374283 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142236 | ACCCTTTTCTCATGT[C/T]TTAAATTATTATTTG | 9690 |
rs767380930 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215356 | TAAAATAAGCATTTG[C/T]ATTTCATTGTATGTA | 9690 |
rs767382969 | snp | A/G | 3.4459e-05 | 0.0041507 | intron-variant | UBE3C | GRCh38.p7 | 7:157182369 | CTGAACACACATATG[A/G]GTAGCATTGGCAGAT | 9690 |
rs767419985 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227319 | GGGTGCTGTGGTCAG[C/G]GGTACTTGCAAGTGG | 9690 |
rs767430639 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152806 | TCCTGTAACTGCTTG[C/G]GAAGTTGAGGACCAC | 9690 |
rs767451038 | in-del | -/C | 1.75311e-05 | 0.00296061 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267774 | GATGCTGGGGTCAGA[-/C]CCCCTACAGAGAACC | 9690 |
rs767461728 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205740 | ATGCAGAGTATCACA[A/C]CTGCAAACATGGATC | 9690 |
rs767462728 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151121 | CGGGGTGAGGGGAGT[C/T]GGGCTCCACCCCCTA | 9690 |
rs767465310 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212254 | GTTACCAGATTTTAC[A/G]TATCACATTTAAGAT | 9690 |
rs767466451 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188730 | TTTATGGCTTAAACA[C/T]ATTAGGTTCTAGTAT | 9690 |
rs767479845 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218869 | TCTGAGTTCGCAAGG[A/G]TGCTAACAAAACCCT | 9690 |
rs767561037 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240932 | TTATCACCAGAGTGT[G/T]TTGGACTCTCAGGAG | 9690 |
rs767588690 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157791 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTGGTC | 9690 |
rs767623453 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192861 | ATAAAAGACATGAAC[-/T]TTAAAAAAAAAAAAA | 9690 |
rs767625840 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137978 | TTCACAATGTCTCTA[C/T]GAAATCATCATGTTG | 9690 |
rs767627554 | snp | A/G | 8.77231e-05 | 0.00662223 | intron-variant | UBE3C | GRCh38.p7 | 7:157187068 | TGCCAGCCAGAGAAC[A/G]TACCTTCCTCCCTGG | 9690 |
rs767646337 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264819 | TCAGGTGATCCACCC[A/G]TTGTGGCCTCCCAAA | 9690 |
rs767657197 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210102 | GAATTGCTAGAACCC[A/G]GGAGGCAGAGGTTGC | 9690 |
rs767662754 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194158 | AAAAGTTGTTTTACC[A/C]CTGGTAATCTTTTTG | 9690 |
rs767671305 | in-del | -/GCACTG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264034 | CACCAGCCTCCCAAA[-/GCACTG]GTACTACAGGTGTGA | 9690 |
rs767709354 | snp | C/T | 0.000151995 | 0.00871633 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267734 | TGCGATTGAATGTGC[C/T]GCTGGCTTTGAGCTG | 9690 |
rs767712017 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219555 | CCATGAGGGTGCAAT[C/T]AGCAAAATCTAGATT | 9690 |
rs767735059 | snp | A/C | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183948 | CTCTCAGTTACCAGT[A/C]TCTCCTGCCAGCGCG | 9690 |
rs767748826 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142108 | TTCTTTGTGGTTTTA[A/G]TTTTGTTTCCTGACA | 9690 |
rs767751832 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182012 | TAGAAGAGTAGATTA[A/T]CCTTTTAGAAGGATA | 9690 |
rs767804317 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170798 | TGCACCCTGAATACC[A/G]CATCATGATTACTTG | 9690 |
rs767815436 | in-del | -/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137565 | CCAGGACTGTATTTC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs767822166 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254213 | TCTTAAAATTTACCT[C/T]AAATGTTATTATTTG | 9690 |
rs767823017 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207843 | GTTCGAGAAGAATAT[A/G]TTACAGCATTTCAGA | 9690 |
rs767829330 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146000 | ACCAAAGCCAAGGTA[A/G]CCTAGATTTTCTCGT | 9690 |
rs767835646 | snp | C/G | 0.000162668 | 0.00901706 | intron-variant | UBE3C | GRCh38.p7 | 7:157164414 | CCTCCCTCATTTTCC[C/G]AAAGTGTTGGGATTA | 9690 |
rs767864696 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225335 | AAAAGATAAGATTTA[A/G]CAGTTTATTCTTTGG | 9690 |
rs767873397 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209339 | TCCTAATGCATCGTT[A/G]AATTTATAATTTGGG | 9690 |
rs767906997 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185063 | GTAGATGGAATGTAG[A/G]TAAATTTTTGTTTTT | 9690 |
rs767947992 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228348 | AATATTGGGAGAAAC[C/T]GTCACATTCCCTCAT | 9690 |
rs767995291 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188577 | AATTGCTGGATTTCA[A/G]TGCATCACTGCCCTG | 9690 |
rs767998135 | snp | C/G | 5.34812e-05 | 0.00517085 | intron-variant | UBE3C | GRCh38.p7 | 7:157170497 | GTTTACACGTGTTCT[C/G]CTTTTTTGTTTAAAG | 9690 |
rs768009660 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161799 | ATTCTAGGCCAAGCA[C/T]GGTGTCTCATGTCTG | 9690 |
rs768020123 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190091 | AGGCGTGAGCCACTG[C/T]GCCCTGCTTAGTTTT | 9690 |
rs768034119 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257302 | GTGAACAAACCGTAC[-/A]ATTTGGAGGGACTAT | 9690 |
rs768076276 | snp | G/T | 6.59826e-05 | 0.00574343 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157163819 | GTGTAGGAGGAAAAG[G/T]CTTCTCTTTTACATC | 9690 |
rs768130499 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189197 | GCTGGAGCAGAAGTG[A/C]TCTTCTGAGTACACT | 9690 |
rs768134875 | snp | C/T | 1.71826e-05 | 0.00293104 | intron-variant | UBE3C | GRCh38.p7 | 7:157178675 | AGTGTGTGAATACTT[C/T]TTTCATTTTTACAGG | 9690 |
rs768147013 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227128 | GCTTATTCAATTTGT[A/G]ATTGAATCCCAGGGG | 9690 |
rs768158990 | in-del | -/A | 1.66441e-05 | 0.00288474 | intron-variant | UBE3C | GRCh38.p7 | 7:157163769 | GGAGTTTTAAAATTG[-/A]AATTATAACCTTACC | 9690 |
rs768159804 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164169 | TTCTTTTTCTTCTCT[C/T]TTTTTTAAGATACTG | 9690 |
rs768211882 | snp | A/G | 1.67256e-05 | 0.0028918 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216870 | CTTTCTTTTCAGGTT[A/G]TCACCAATCTAGTGA | 9690 |
rs768224119 | snp | A/G | 1.79961e-05 | 0.00299962 | intron-variant | UBE3C | GRCh38.p7 | 7:157170276 | AAATACTATATTTAT[A/G]GGTCATTTTGTTTTG | 9690 |
rs768227463 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201303 | CACTCCAGCCTGGGC[A/T]ACAGAGCAAGACCCT | 9690 |
rs768291381 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143021 | TACAGGCCTGCACCA[A/C]CACGTCTGGCTAATT | 9690 |
rs768296519 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151076 | AGCCTGTGGTGACTT[C/T]GGTCATGGTGTATTT | 9690 |
rs768297135 | snp | C/G | 1.65266e-05 | 0.00287455 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231284 | TGCTTGTGGGAGATT[C/G]TTTTGCCAGACATTA | 9690 |
rs768351982 | snp | A/G | 1.65627e-05 | 0.00287769 | intron-variant | UBE3C | GRCh38.p7 | 7:157220675 | GAGTTCTGAACCAGG[A/G]TTGCCCCCGACAGGT | 9690 |
rs768384991 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206293 | TTGGAAACGGAGTCT[C/T]GCCCTGTTGCCCAGG | 9690 |
rs768399948 | snp | C/T | 1.67787e-05 | 0.00289639 | intron-variant | UBE3C | GRCh38.p7 | 7:157231038 | ATGTTATTGCTTGCT[C/T]GTAACATCTTTCCTC | 9690 |
rs768404612 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154509 | TCAACAAAATATCTT[-/A]AGTGATTCCATATCG | 9690 |
rs768409567 | in-del | -/TTTTTC | 1.64754e-05 | 0.00287009 | intron-variant | UBE3C | GRCh38.p7 | 7:157182094 | TATAAAAAGCTTCTG[-/TTTTTC]TTTTTCAGGCAACAA | 9690 |
rs768440815 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246137 | GTATCAGTGGACGAG[G/T]CCTTAAAATGTGAAT | 9690 |
rs768452862 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267687 | CTCCCCGAGTTCTAT[A/G]ACGAGACACTTTTGC | 9690 |
rs768460802 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145858 | CACGCTGTTTCCTTT[A/G]TTATTTACATCTTGT | 9690 |
rs768463008 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221814 | TTGTGTCTACCAGCC[A/G]ACTAATGATATTCAG | 9690 |
rs768476586 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141127 | TGCTAACCCTGAGCC[A/G]AGGGCCATTCTTCTG | 9690 |
rs768496452 | snp | C/T | 6.76232e-05 | 0.00581438 | missense, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139301 | AAGGCGACTTCAAGA[C/T]GCGGCCCAAGGTGTC | 9690 |
rs768500703 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189755 | GTGGGTTCTTTTTTC[-/C]TCCTCTTTCTCACTC | 9690 |
rs768558474 | snp | C/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173389 | TCTCAAGCATAGATG[C/G/T]GATAGCAATAAATTA | 9690 |
rs768583822 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224652 | AAGATTACTTGGTTC[C/T]GTTCTTCAGTAATGG | 9690 |
rs768614218 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225417 | GTTAGATCTTTCAGA[A/G]GTTGATTTATGCAGA | 9690 |
rs768624560 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147733 | CTCTATTCCTAGTTT[A/G]CAGAATTTTATCATG | 9690 |
rs768652337 | snp | C/G | 1.67181e-05 | 0.00289115 | intron-variant | UBE3C | GRCh38.p7 | 7:157254194 | ACAGGAAATGAACAG[C/G]CTTTCTTAAAATTTA | 9690 |
rs768675801 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214815 | CTTTCAAGAATTAGT[A/G]TATTAGGTCAATGAC | 9690 |
rs768687321 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216335 | TCAGATGAGCTAAGA[C/T]ATTTCCAGATTCGTG | 9690 |
rs768709240 | in-del | -/TATTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242400 | AGATTTCTAGTCTGA[-/TATTT]TATTCTCCTATATGG | 9690 |
rs768730941 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165042 | ATGGCCTCTACCCAC[A/T]AAATGCCAGTAGCAC | 9690 |
rs768734688 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146942 | GGGAGTGAGACACCG[C/T]GCCCAACCATAGTAA | 9690 |
rs768781322 | snp | C/T | 1.64969e-05 | 0.00287196 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254016 | CAACCGGATTGCGTA[C/T]ATCCACTTGGTGGCA | 9690 |
rs768812763 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229168 | CCTCTCCTTCCCCCT[A/G]TCTTTTCTGCAAAGC | 9690 |
rs768839052 | snp | A/T | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170397 | CCCAACCTTACCCTT[A/T]TGGTAAGGCAGCTTC | 9690 |
rs768845472 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222321 | AGGAGGAGAAGTTTT[A/G]AATTTTGATAGAATC | 9690 |
rs768878232 | snp | A/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207782 | ATGCCTTCGAGATGC[A/T]TGCCTGGGGATCATC | 9690 |
rs768913585 | in-del | -/AAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163389 | GAGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAGG | 9690 |
rs768917497 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175660 | CTGTCTGTAATATTT[A/G]TTTAGGATTACTGTC | 9690 |
rs768917749 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183883 | TTTTGCAAAGGGGCC[C/T]TCTCTGAGGAAGGGC | 9690 |
rs768933375 | snp | C/T | | | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269686 | TTTGTTTGCCCTTTT[C/T]TACGTTCTGTCCTAC | 9690 |
rs768940804 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168474 | AAAACCTGTATCCAC[A/G]ACAAAACTTATATAT | 9690 |
rs768967721 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239654 | AAAACTTGAGCAGCC[A/G]CTTAAGGGATATGGG | 9690 |
rs768979987 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265609 | TGTGCATGGAACACC[A/G]TATAGCCTCACCATT | 9690 |
rs769009524 | in-del | -/A | 1.64746e-05 | 0.00287002 | intron-variant | UBE3C | GRCh38.p7 | 7:157267570 | TGACATCTTGCACAC[-/A]ATGCTGTTTTTCAGG | 9690 |
rs769012617 | in-del | -/ATG | | | cds-indel, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268379 | ACCGTGGCCTGCCTC[-/ATG]ATGGTTTGGAGATAC | 9690 |
rs769065127 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169875 | TTTTAGTAGAGATGG[C/T]GTTTCACCATGTTGC | 9690 |
rs769067256 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156714 | AATTCCCTTCTTTTT[A/T]AAAAAAAAAAAAAAA | 9690 |
rs769120235 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157781 | ACAGTTTGAGACCAG[C/G]CTGGCCAACGTGGTG | 9690 |
rs769126449 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258513 | GCTGGAGTGCAGAGG[A/G]CAATGGCGTGATTTC | 9690 |
rs769132357 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242396 | CGACAGATTTCTAGT[C/G]TGATATTTTATTCTC | 9690 |
rs769171478 | snp | A/G | 1.7294e-05 | 0.00294053 | intron-variant | UBE3C | GRCh38.p7 | 7:157223214 | GGGAATGCAGGGGAA[A/G]GTACAAGTGAACTAA | 9690 |
rs769174749 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198185 | AACATCTTGTAGCTG[A/C]TTTTCTCCATGCATA | 9690 |
rs769180782 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240673 | TCTAGGCTGTTTAGA[G/T]AGGAAATTAATCCGT | 9690 |
rs769210814 | in-del | -/GAGACA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225033 | TTTTATTTTATTTTT[-/GAGACA]GAGATTCACTCTGTC | 9690 |
rs769216295 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247339 | TCTAGCACAGTGCCT[A/G]GCACCTAGTACCTAG | 9690 |
rs769231458 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197161 | CAAAATCAAACTAGA[C/T]ACTTTTCAGTATTTA | 9690 |
rs769247187 | snp | C/T | 1.65053e-05 | 0.0028727 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184026 | CGACAAGCCCTCAAG[C/T]CCGGTAAGCCCCGTG | 9690 |
rs769254199 | snp | A/G | 2.14797e-05 | 0.0032771 | intron-variant | UBE3C | GRCh38.p7 | 7:157207942 | TTATTTAAGGTATAG[A/G]GTATATGTATTTTTT | 9690 |
rs769261892 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195879 | GTGGTGGCGGGGCGG[A/G]GGTTGCACTGTAGTA | 9690 |
rs769288523 | snp | A/T | 1.73881e-05 | 0.00294852 | intron-variant | UBE3C | GRCh38.p7 | 7:157216848 | ACGTGTGTGACGCGG[A/T]TATGTTCTTTCTTTT | 9690 |
rs769300854 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239326 | CCTAACATTGAGTTG[-/A]AGAATCCAGACACAC | 9690 |
rs769354197 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190358 | TGAACAGGCCCGTCA[G/T]CTACTTGGTTGTCTG | 9690 |
rs769425274 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226323 | TAGCATTTGGAGCTC[A/G]CTGGCACGTTTCGTC | 9690 |
rs769426197 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153871 | TGGTATATGTACCTG[C/T]GGTTTCAGTTACTCG | 9690 |
rs769442955 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160405 | TTAAAAATACAGTTT[A/T]CATTGTATTTAATTT | 9690 |
rs769459166 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260435 | AGCATGACCCATGTG[A/T]CCAGATAGGAGAATC | 9690 |
rs769509452 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188485 | TTGCATGAGAGCAGG[A/T]TGTGAGATCTGAGGA | 9690 |
rs769511261 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216466 | CTCAGGTATTAAGCT[C/T]GGTCCCCAGTAGTCA | 9690 |
rs769514515 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant | UBE3C | GRCh38.p7 | 7:157169025 | TGACCAATTGCTCCC[C/T]CACTCCTCCTTTTAT | 9690 |
rs769532511 | snp | A/C | 3.30447e-05 | 0.00406464 | intron-variant | UBE3C | GRCh38.p7 | 7:157257092 | CCACTTCATAATAAG[A/C]AAGGCAGCAGAACAT | 9690 |
rs769545173 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260951 | GGCCACTTGTGCTGC[A/G]TGAGCGTCGTAGGTT | 9690 |
rs769566129 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161669 | ATGTAGCCCAGGCTG[G/T]TCTCATACTCCTGAG | 9690 |
rs769579536 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142068 | CTTGATATTGCAAGT[A/C]CTTTAATTTTAGTGA | 9690 |
rs769602794 | snp | A/G | 0.000487607 | 0.0156066 | intron-variant | UBE3C | GRCh38.p7 | 7:157164382 | GGCTGATTTCAAACT[A/G]TGGCCTCATGCAATC | 9690 |
rs769615433 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251744 | GTCCCTCAGATCTGA[A/C]ATTTAGCACTTATGT | 9690 |
rs769624399 | in-del | -/AAATGTGTATTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198927 | GAAATACAAATTTTA[-/AAATGTGTATTTT]AAATGTGTATTTCTG | 9690 |
rs769634655 | snp | A/G | 1.75863e-05 | 0.00296527 | intron-variant | UBE3C | GRCh38.p7 | 7:157178652 | TGGTGACATTTTGCC[A/G]TCCTGTAAGTGTGTG | 9690 |
rs769646685 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192159 | TCAGCAATATCATTC[A/C]TAGTTCTGAATCTTC | 9690 |
rs769702151 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148764 | TCCTTTAAGAGACAG[C/G]GCCTCACTGTGTCGC | 9690 |
rs769714961 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266258 | GGCGGATGTTGCAGT[A/G]AGCCGAGATTGCACC | 9690 |
rs769723359 | in-del | -/CTTTTTTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160069 | GTAATTCCGTAGTTA[-/CTTTTTTTTTT]CTTTTTTTTTTCTGA | 9690 |
rs769728213 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157175000 | AGACTTACATGCTTA[C/T]TTCAGATAAAAAGAT | 9690 |
rs769740000 | snp | A/T | 1.66846e-05 | 0.00288826 | intron-variant | UBE3C | GRCh38.p7 | 7:157182337 | TATTTGGGTATGAAA[A/T]ACAAGATCTTTTTTA | 9690 |
rs769758867 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244707 | ATTTGCATTAATTGC[A/G]TCGCGACTGCACTCA | 9690 |
rs769760751 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172403 | TCAAATTGCATGAAA[G/T]GGGAGTATACAGTGA | 9690 |
rs769762458 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233909 | AGTGGGTGGGAATTG[C/G]TATCTCATTGTGGTT | 9690 |
rs769766308 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149706 | GTTGAAAAAATAGAT[-/G]GTCTCATAAGACCAT | 9690 |
rs769768469 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157585 | GACCTACAAAGAAAT[G/T]TAACCTGCAGACATT | 9690 |
rs769772890 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143977 | GGGAGTGAATCTCAG[A/G]GAGGGAGGAGTGACA | 9690 |
rs769795817 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220506 | CTGTAAAAGTATGAA[A/G]GGACAGCTAGCATGA | 9690 |
rs769826335 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant | UBE3C | GRCh38.p7 | 7:157248621 | ATACCTGTATAGCAA[A/G]TAGCAGCATCTCCTT | 9690 |
rs769844686 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197432 | TCTATTCCTAATCCA[A/G]ATTTGTCTATATTCA | 9690 |
rs769861858 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156618 | CCCCAATTCTTTAAT[C/G]CTTACATTCACACTC | 9690 |
rs769889030 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174437 | TGTGTTATTTTAAGA[C/T]TGAAAATGCAAATAC | 9690 |
rs769893274 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146876 | GGCTGGTCTTGAACT[A/C]CTGACCTGAAGTGAT | 9690 |
rs769895762 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218543 | ATGACTATGTCCTCA[C/T]AAGATATTTGTGAGT | 9690 |
rs769898699 | snp | C/G | 1.77131e-05 | 0.00297594 | intron-variant | UBE3C | GRCh38.p7 | 7:157170300 | TGTTTTGTTTTTCTT[C/G]CAGTATTCCATCCAA | 9690 |
rs769921324 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145649 | TATAGTTGGAATCAT[A/G]TACTATGTAATCTTT | 9690 |
rs769953235 | in-del | -/CACACT/CACT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224792 | ACACACACACACACA[-/CACACT/CACT]CTCTCTCTCTCTCTC | 9690 |
rs769979817 | in-del | -/CAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245283 | CTAATGCAGAAATGG[-/CAAA]CAGTGACCTTATATA | 9690 |
rs769984704 | snp | G/T | 0.000214142 | 0.0103453 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182259 | TTAATAGAGAGTAGA[G/T]GTTCAAGAAAGAGTG | 9690 |
rs770003999 | in-del | -/TTA | 1.70197e-05 | 0.00291711 | intron-variant | UBE3C | GRCh38.p7 | 7:157223370 | TGCAATTTGGCTTCT[-/TTA]TTGTCACTACGTATC | 9690 |
rs770036101 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213332 | ACCTATCAGAGTCAT[C/T]TGGGGGAGCAGTTGA | 9690 |
rs770050411 | in-del | -/CAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219329 | AGTCCCTTATCTCAT[-/CAC]CAGCTGGTAGTACGG | 9690 |
rs770065768 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240629 | AATTGGTTGCAAGTT[C/T]AGAGTGGTTACAAGA | 9690 |
rs770076723 | snp | C/T | 6.83293e-05 | 0.00584466 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139254 | GCGGCGCTGCCCGCA[C/T]ATGGGCTAGGCTGCC | 9690 |
rs770081651 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177959 | TAAGAAAAAGGAAAA[A/G]CAGCTGTAAAATACC | 9690 |
rs770126318 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142119 | TTTAATTTTGTTTCC[C/T]GACAACTAATTATGT | 9690 |
rs770150348 | snp | C/T | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267714 | TTGCGAAGTAAACTT[C/T]TCTATGCGATTGAAT | 9690 |
rs770180143 | snp | A/G | 3.29962e-05 | 0.00406165 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220735 | ATGTGTGGAGGTTCC[A/G]GCGGATGGGGAGGAT | 9690 |
rs770206082 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167326 | GTGTGTTAGTCTCAG[C/G]TTTGTAGATGGCATT | 9690 |
rs770228609 | in-del | -/TTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140792 | CTGAGGGAGTGAGAT[-/TTC]TTAACTGTTGATCAG | 9690 |
rs770239316 | snp | C/T | 1.65562e-05 | 0.00287712 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170381 | TCCCATTGCTAATGG[C/T]CCCAACCTTACCCTT | 9690 |
rs770260656 | snp | A/G | 1.70429e-05 | 0.0029191 | intron-variant | UBE3C | GRCh38.p7 | 7:157220806 | ACACAGGGTTACTGA[A/G]GTATGAATTACATGC | 9690 |
rs770293077 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241384 | TATATGAAGGACTCC[A/G]TGATAAAAATGGGCG | 9690 |
rs770303729 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231791 | ATAAGAAATGGATTT[C/T]AGTTTTTATTAATTA | 9690 |
rs770306866 | in-del | -/TGAAA | 1.64792e-05 | 0.00287042 | intron-variant | UBE3C | GRCh38.p7 | 7:157254358 | ATGTTGCAGGTGGTC[-/TGAAA]ATATTTCCAAAGTAA | 9690 |
rs770317282 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209038 | TCTATTTAATTGAAA[A/G]AAGTTAATTGAATGA | 9690 |
rs770338188 | snp | C/T | 0.000115326 | 0.00759274 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207479 | AATCATCCCACTCTT[C/T]TATCTTTTTAGCTCC | 9690 |
rs770340582 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206284 | TTATTTTTTTTGGAA[A/G]CGGAGTCTCGCCCTG | 9690 |
rs770355548 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199270 | CGTAGCTTTTTTCTT[A/G]CTCTTTTTTCCGTAT | 9690 |
rs770382381 | in-del | -/TTAT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269309 | TCAGCTATTCTGAGC[-/TTAT]TTATTTATTTATTTG | 9690 |
rs770384991 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233127 | TTCTAGACATTTCAT[A/G]TAAGTGGAATCATTT | 9690 |
rs770391742 | in-del | -/ATA | 1.6516e-05 | 0.00287362 | intron-variant | UBE3C | GRCh38.p7 | 7:157257084 | TTTAAAGACCACTTC[-/ATA]ATAAGAAAGGCAGCA | 9690 |
rs770444683 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220357 | AGTGAATTTTTGATA[A/G]TAATAACTTAATTTT | 9690 |
rs770451377 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242852 | ACGAGGTCAGGAGTT[C/T]TAGACCAGCCTGACC | 9690 |
rs770455400 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194725 | TAGAAAATGAGGAAT[A/G]TGTTATTGGAAAACT | 9690 |
rs770466221 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189677 | CCTGACTCTTTCAGC[A/G]GCTTCTTTCATAGAT | 9690 |
rs770476004 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197423 | ATCTTAAGGTCTATT[C/G]CTAATCCAGATTTGT | 9690 |
rs770488267 | snp | C/T | 3.30049e-05 | 0.00406219 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231249 | TGAAGGGCTTCTGTA[C/T]CCCAACCCGGCTGCT | 9690 |
rs770500255 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181528 | TTTAGGGTATTATAG[A/G]TCTCTATATTTGTTG | 9690 |
rs770506610 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241251 | GTCTTAGCTGTGAGA[A/C]CAGGAGCACAAAAAA | 9690 |
rs770529178 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244254 | AAAAGAAAGAAAGAT[A/G]AGGTATATCTCCTGC | 9690 |
rs770532395 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209777 | ATATAAGATATTTTC[C/T]ACCCTGGCCTTATTT | 9690 |
rs770536924 | snp | A/G | 1.65641e-05 | 0.00287781 | intron-variant | UBE3C | GRCh38.p7 | 7:157163898 | ACTCTGTAGATAAGC[A/G]TTTTTTCTACAGCAT | 9690 |
rs770539973 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235707 | ATAAAGTTTAGACCA[A/G]TAACAAAACTAAGAG | 9690 |
rs770570059 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231820 | TACTCAGTTTCAGGT[-/C]TTCTGTTATAAGCAG | 9690 |
rs770586921 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262254 | CATTTTTATGAGAGA[-/T]TTAAAGGAGCAAATA | 9690 |
rs770589650 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159404 | GGTGAATGGATAAAG[A/G]CAGTCTCCCCCTACC | 9690 |
rs770607677 | snp | A/T | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174990 | TGGATCTGAGAGACT[A/T]ACATGCTTATTTCAG | 9690 |
rs770624842 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181622 | ATTTTGCTAGAGAAT[A/G]TTCTAAAACCATTGC | 9690 |
rs770626690 | snp | A/C | 1.66167e-05 | 0.00288237 | intron-variant | UBE3C | GRCh38.p7 | 7:157163776 | TAAAATTGAAATTAT[A/C]ACCTTACCTCCTTTT | 9690 |
rs770667350 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225143 | AAGTAGCTGGGATTA[C/T]AGGCATGAGCCAATG | 9690 |
rs770679995 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172471 | AATGATCCTACTTGA[A/G]TTAATTACAGCGGAC | 9690 |
rs770697534 | snp | C/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184012 | GAGAGTGAAGAAGCC[C/G]ACAAGCCCTCAAGCC | 9690 |
rs770712137 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191206 | GTGATTTAGATAAAC[-/A]AGCGGTGCGCCTCGA | 9690 |
rs770712298 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186042 | AAATGAGTAAATTGC[A/G]TAGATTGGCTTGGGT | 9690 |
rs770714562 | snp | C/G | 1.65592e-05 | 0.00287738 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181530 | TAGGGTATTATAGGT[C/G]TCTATATTTGTTGAT | 9690 |
rs770720350 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175530 | AGTGATGTGAGTTAC[A/G]TTACCTGAATATAAC | 9690 |
rs770723347 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152585 | TTTCGTTTATGAGCT[C/T]ATTGATCTCGACTTC | 9690 |
rs770738597 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202375 | CCAGAAGTCTAAGCC[A/G]GCCGGGCGCGGTGGC | 9690 |
rs770757186 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236485 | AATTTTTTATCGCGG[A/T]AGAATTCAGTGTGCA | 9690 |
rs770775950 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192612 | AAGAAAAGGAAGGAG[G/T]CTTACCCCACTCCCA | 9690 |
rs770795711 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219268 | GAAAATGTCAGCTGA[A/T]CCCAGCAGTGTGCTT | 9690 |
rs770807428 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252659 | CACATTTGTGAAACA[A/G]TCTTTCTGTAAATGG | 9690 |
rs770845819 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254816 | AGGCCGGGGCAGGTG[G/T]ATCACTTGAGCTCAG | 9690 |
rs770865191 | snp | A/G | 3.30169e-05 | 0.00406293 | intron-variant | UBE3C | GRCh38.p7 | 7:157207395 | TCTTTTCTTTAATTC[A/G]AGGTCTATGGTACCG | 9690 |
rs770866233 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254259 | GTATTAATTTCTGGT[A/G]CACAAGTTCCCATAA | 9690 |
rs770903326 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141936 | GCACATAATACTCTT[G/T]TGCTGGGTCCTAGAT | 9690 |
rs770919754 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253935 | AGGATTTTGAGATCC[A/T]TACGTTTTGTATTCC | 9690 |
rs770924356 | snp | A/G | 6.59065e-05 | 0.00574012 | intron-variant | UBE3C | GRCh38.p7 | 7:157267545 | CTCATGTAATGCCAT[A/G]CTTGTTACAGTGACA | 9690 |
rs770929301 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228814 | TCAGTCAGTCCAGTA[A/G]ATTGTATTTGCCCTA | 9690 |
rs770948332 | snp | A/G | 1.68624e-05 | 0.0029036 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182135 | TACAGCCTTCACAGA[A/G]GAGTTTCTGGCAGCA | 9690 |
rs770985491 | snp | A/G/T | 3.30574e-05 | 0.00406544 | intron-variant | UBE3C | GRCh38.p7 | 7:157225388 | TTCTAATAACCTTAC[A/G/T]GCTTTCCTTGTTTGT | 9690 |
rs770987024 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231586 | CTTTAAGAGGTGATT[A/G]GATCATGTGAGCTCG | 9690 |
rs771010304 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257207 | ATATATTTTGGTGCT[A/G]GTTTTATTTGGGGTT | 9690 |
rs771013104 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180487 | GATAAAGTACTGAGT[A/G]TGCATTGTTTGGTGA | 9690 |
rs771065499 | in-del | -/CA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155416 | GTGAAACAAAAACCT[-/CA]CAGTTTTTTGGGGTT | 9690 |
rs771077045 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232859 | GCAAAACAGGTGGTG[C/T]TTTTAGGACTTCTTT | 9690 |
rs771077179 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221938 | GCAGAGGCGCAATCA[C/T]GGCTCACTGCAGCCT | 9690 |
rs771079771 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183739 | CTAAATATGTTTCCT[A/G]TTATAACACAGTTAG | 9690 |
rs771085541 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211100 | GTTTCCTCCTGTGAT[A/G]GGGAAACAGGAGGAA | 9690 |
rs771164010 | snp | A/T | 1.69968e-05 | 0.00291515 | intron-variant | UBE3C | GRCh38.p7 | 7:157223366 | GGTATGCAATTTGGC[A/T]TCTTTATTGTCACTA | 9690 |
rs771192647 | in-del | -/TTAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216816 | ATGGCTCACTGTGCA[-/TTAT]TTGTGCTGCCGAGCT | 9690 |
rs771214490 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248967 | CAGCTGCTCCAGCAC[C/T]GTCTAGGGGGTGTGT | 9690 |
rs771218878 | snp | A/C/T | 1.71146e-05 | 0.00292524 | intron-variant | UBE3C | GRCh38.p7 | 7:157175081 | TAATGTATTGATCAC[A/C/T]TTGTCTAGGGGAACA | 9690 |
rs771227210 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258209 | ACTTCAGCCTCCCAA[A/G]GTGCTGGGATGACAG | 9690 |
rs771234943 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234767 | TCAGGTGTTGATTTG[A/T]TGTTGATTTGTGAGT | 9690 |
rs771246706 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176968 | TTTTTCTTTTTCTGT[-/A]AATGTGGCCTTCCAG | 9690 |
rs771252696 | snp | A/G | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170361 | TCACAGTCCGGGGGC[A/G]CTTTTCCCATTGCTA | 9690 |
rs771270830 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144274 | GCACTCCAGCCTAGG[C/T]GACACAGCATGACCC | 9690 |
rs771302353 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239911 | ATCCCACTGTTGCTG[C/T]TTTCTGGGTGATGCA | 9690 |
rs771312830 | in-del | -/A | 3.3461e-05 | 0.00409016 | intron-variant | UBE3C | GRCh38.p7 | 7:157183851 | ATGTTTAACTAAAAT[-/A]ACGTTTTAACTGATT | 9690 |
rs771314555 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248443 | CTTGGAACCAGTGCC[A/G]ACGTGGACATTCACC | 9690 |
rs771316706 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166282 | TCTTGAAGCTTTCAA[A/G]TGTATTTTGTATTTC | 9690 |
rs771320017 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246309 | GACTCACTCCCCACA[G/T]GAGCAGTGGCTCACA | 9690 |
rs771340555 | snp | A/G | 3.57756e-05 | 0.00422925 | intron-variant | UBE3C | GRCh38.p7 | 7:157170286 | TTTATGGGTCATTTT[A/G]TTTTGTTTTTCTTCC | 9690 |
rs771353094 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188396 | TCACTCACTGGTGTT[G/T]ATTACCATCGGAGGA | 9690 |
rs771358393 | snp | A/C | 1.65053e-05 | 0.0028727 | synonymous-codon, intron-variant | UBE3C | GRCh38.p7 | 7:157220691 | TTGCCCCCGACAGGT[A/C]ACTCAGCTCTATGTG | 9690 |
rs771419304 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250129 | GTTCCAGAGACTGGC[C/T]GGGAGGTGTGATGCC | 9690 |
rs771437517 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152507 | AGGATGTTTGTGTTT[C/T]TCTCCTTGTTTGTCA | 9690 |
rs771449891 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177892 | AAACAGCCTCCTGGG[C/T]CCCTCATTAAAGGTG | 9690 |
rs771459825 | snp | C/T | 2.27498e-05 | 0.00337259 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139317 | GCGGCCCAAGGTGTC[C/T]CTTGGCGGCGCGAGC | 9690 |
rs771483419 | snp | C/T | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216898 | TGAAAATGTTGAAGT[C/T]CAGAGACACGAGGAG | 9690 |
rs771509241 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240471 | GTAGGGCCCACTTGA[C/T]GTTAATATCATAAAG | 9690 |
rs771527632 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266752 | TTTTAAAAAATTTTT[A/G]TAGACAGGGTCTCAC | 9690 |
rs771527729 | in-del | -/G | 1.6996e-05 | 0.00291508 | intron-variant | UBE3C | GRCh38.p7 | 7:157220804 | GGACACAGGGTTACT[-/G]AGGTATGAATTACAT | 9690 |
rs771534714 | snp | C/T | 1.79027e-05 | 0.00299183 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267798 | GAGAACCAGTGCTTC[C/T]TTCGTCAGCAGCGCC | 9690 |
rs771534763 | snp | C/T | 1.6607e-05 | 0.00288153 | intron-variant | UBE3C | GRCh38.p7 | 7:157231062 | TTTCCTCCTCACCCT[C/T]CCATTTTTTTTTAAC | 9690 |
rs771534819 | in-del | -/TTTGGGTAT | 1.65296e-05 | 0.00287481 | intron-variant | UBE3C | GRCh38.p7 | 7:157182324 | TGTTGGCGAAAATTA[-/TTTGGGTAT]GAAATACAAGATCTT | 9690 |
rs771586088 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267695 | GTTCTATGACGAGAC[A/G]CTTTTGCGAAGTAAA | 9690 |
rs771587307 | snp | C/T | 1.70866e-05 | 0.00292284 | intron-variant | UBE3C | GRCh38.p7 | 7:157181501 | ACTAAATTTTAAATA[C/T]GTGTTTTTCCTTTTA | 9690 |
rs771604442 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229556 | TCCTGCCCTCAGGTG[A/G]CCCACCTGCCTTGGC | 9690 |
rs771609472 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228683 | AGAGGTGGCGGGCAC[A/G]GCAGGGCAGCACTGC | 9690 |
rs771611763 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153477 | TCTAATTTGTTTTTA[A/G]CAGAGTCCAGGTCTC | 9690 |
rs771637169 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178970 | TACTGGTGTCCCAGA[C/T]GCCTTGTGCTCCATC | 9690 |
rs771646742 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178931 | TGCTGTGAGCCTGTG[A/C]CCTCAGTCTCAATGT | 9690 |
rs771648925 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190476 | GTCCTCGGCTACCAA[A/G]GCCACATTTCAAGTG | 9690 |
rs771692460 | in-del | -/T | 0.000105402 | 0.00725877 | intron-variant | UBE3C | GRCh38.p7 | 7:157217022 | AAAAATACATTCAGC[-/T]TGTGTCTTTCTGGAG | 9690 |
rs771706596 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269199 | GTTGAATGTTCTATA[-/T]CTTATTAGTTAATTT | 9690 |
rs771711166 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183909 | AGGGCTGCTGGTGTA[C/T]TTGCGGGTGCTGCAG | 9690 |
rs771747480 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208945 | TCCGTTTAATACCAG[C/T]GACCTCTCGCACACT | 9690 |
rs771773610 | snp | C/T | 3.78852e-05 | 0.00435215 | intron-variant | UBE3C | GRCh38.p7 | 7:157187030 | AAGTCAGGCAAGTGT[C/T]CGTGGGCGTCTGTGC | 9690 |
rs771775413 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180248 | CATGAAGCTTTTTAA[C/T]ATTTGCAACAGAACC | 9690 |
rs771784208 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173559 | TCACCTCCTTTTTAA[A/G]AAATTTTTCTTACGA | 9690 |
rs771799262 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207730 | GACAATCATCAATGA[C/T]GCCTTTTACTTTAGA | 9690 |
rs771861406 | snp | G/T | 8.38539e-05 | 0.00647456 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186925 | CCCTGCTCAACCTGG[G/T]GTGGAGGGACTCTGC | 9690 |
rs771869250 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218581 | GTTGCATCTAACTCT[A/G]CCCACTGACAAGGTA | 9690 |
rs771898179 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234053 | TATTAAGTCCCTGCA[A/G]TGCAATGAATTATGA | 9690 |
rs771908932 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162025 | CAGTGAGCCAAGATC[A/G]CCACTACACTCCAGC | 9690 |
rs771909712 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202290 | TATGTAATAGGTAGG[A/C]ATTTCATACTTAAAA | 9690 |
rs771910833 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174300 | TATATGAGAAATACC[A/G]TATTTCTCATATATT | 9690 |
rs771918858 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174724 | CCCAAAGTTACAGAC[A/G]TGAACCACTGTGCCT | 9690 |
rs771963801 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238901 | GTGCCAAATAAAGAC[-/AG]TGTTTGAAAGGAAGA | 9690 |
rs771970655 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186603 | GAAGCTACTGTTATA[-/T]CATAGGCAAAAACCG | 9690 |
rs771976329 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263091 | CTCACATCTCTTTAT[A/T]TCCAGCATCCTCTTA | 9690 |
rs771978259 | snp | C/T | 4.9489e-05 | 0.00497414 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231234 | CTTTAAGACTACTAA[C/T]GAAGGGCTTCTGTAC | 9690 |
rs771983129 | snp | A/G | 5.02105e-05 | 0.00501026 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223345 | TCCATTTGAGGAACG[A/G]GTAAAGGTATGCAAT | 9690 |
rs771997438 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159736 | GCCGAGCGTGGTGGC[A/G]CATGGTAATCCCGGC | 9690 |
rs772053940 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209261 | ACAACACATTTCTCT[C/T]AGGAGCATGAGCATT | 9690 |
rs772070095 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255134 | TCTAAATAGATAAAT[A/G]TATACATACACAACG | 9690 |
rs772073555 | snp | C/T | 1.66438e-05 | 0.00288472 | intron-variant | UBE3C | GRCh38.p7 | 7:157163766 | ATGGGAGTTTTAAAA[C/T]TGAAATTATAACCTT | 9690 |
rs772094862 | snp | A/G | 3.62168e-05 | 0.00425524 | intron-variant | UBE3C | GRCh38.p7 | 7:157188986 | CCTTTGTACCCTGAC[A/G]TGGAAAGATTTCCGA | 9690 |
rs772105771 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205111 | GTCTTTGAGACTGAC[A/C]TGTTTTCAGAGGAAT | 9690 |
rs772118008 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230620 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 9690 |
rs772145011 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183462 | GCTCATTGTGTCTTC[C/T]TGTTGAGTTTTATGG | 9690 |
rs772164081 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189840 | GTCTCTTGCCTTGTC[A/G]CCCAGGCTGGAGTGC | 9690 |
rs772165457 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203933 | CTAGCCTACCTAAAA[C/T]GTGCTCAAAATATGT | 9690 |
rs772168319 | snp | A/C | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138222 | ACTTACAATATTTTC[A/C]TCTTACGATGGGTTT | 9690 |
rs772182938 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191510 | TGCCTAGGCTGGTCT[C/T]GAACACCTGGGCCCA | 9690 |
rs772184896 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251629 | GATTCCAAGTGAAAA[C/T]AGACTTTCTGGAGGA | 9690 |
rs772201769 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220907 | CAGGAGCTACCATGT[A/G]GAAAAGTTTCATCAC | 9690 |
rs772257438 | snp | A/G | 1.67139e-05 | 0.00289079 | intron-variant | UBE3C | GRCh38.p7 | 7:157223223 | GGGGAAAGTACAAGT[A/G]AACTAATTAAGGTTT | 9690 |
rs772279703 | in-del | -/AT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164505 | GCTCACTGTTAAGAC[-/AT]GTGTCTTAACTGTTT | 9690 |
rs772281707 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171147 | AGGGCACTGAGGGAG[C/T]AGAGCCTTGCTCTTG | 9690 |
rs772312872 | snp | C/T | 1.66167e-05 | 0.00288237 | intron-variant | UBE3C | GRCh38.p7 | 7:157254239 | ATTTGAACTTTTTTC[C/T]TTAGGTATTAATTTC | 9690 |
rs772322195 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242973 | GGTAGGAAAATCGCT[C/T]GAAACCGGAAGGCAG | 9690 |
rs772330728 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259403 | GATGTCGCAGCCCCA[C/T]CGTTGGGAGTGTACA | 9690 |
rs772332748 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159210 | ACCATGGCATACACA[A/C]CATGATTGTGGAGGA | 9690 |
rs772339443 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183982 | TGTCACGACTCAGCC[A/G]GTGACTCTGAGGAGG | 9690 |
rs772389802 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166915 | CGCTTTTTCCTGTTG[G/T]TGGTGGTGGTGGTGG | 9690 |
rs772409167 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197325 | CAAAACATTAACACT[A/C]AGTATGTAACAAACT | 9690 |
rs772442004 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147079 | ACAAAAAAAACCTGT[A/G]GAATTTTGATTGGGA | 9690 |
rs772451131 | in-del | -/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137932 | AGATTTTATGTACTC[-/T]TTACCACACACACAC | 9690 |
rs772459679 | snp | C/T | 1.65089e-05 | 0.00287301 | intron-variant | UBE3C | GRCh38.p7 | 7:157169041 | CACTCCTCCTTTTAT[C/T]GTTTAGGAAGAAAGG | 9690 |
rs772465840 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266182 | AGCCGGGCGTGGTGG[C/T]GGGAGCCTGTAGTCC | 9690 |
rs772490383 | snp | C/T | 0.000171836 | 0.0092676 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182125 | AACAAGTTTTTACAG[C/T]CTTCACAGAGGAGTT | 9690 |
rs772495759 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248406 | GGAGCTGCCCTTTGC[A/G]GGCTTCTTTCTTTCC | 9690 |
rs772540763 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195713 | AATTTAGATGGCTTT[A/G]GTGTGAGATTTGAGA | 9690 |
rs772560900 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234724 | TATATCATCATCTTC[A/T]GGCTCACCGTATTTC | 9690 |
rs772568057 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147826 | CTGCAGCTTGTGGAT[A/G]TGATGGATCACATTA | 9690 |
rs772586192 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260156 | ACAGGACAAACAGAA[C/T]CAACTCTGTTTACCA | 9690 |
rs772605615 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219247 | CTCCAGAAAGTTGTG[C/T]GATGGGAAAATGTCA | 9690 |
rs772606319 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242526 | TTGTTTTTTTTTTTT[-/TG]TTTTTTTTTTTAAAT | 9690 |
rs772617500 | in-del | -/GAGAGAGAGA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211169 | ATCCATATGTCTGGA[-/GAGAGAGAGA]GAGAGAGAGAGAGAG | 9690 |
rs772618473 | snp | A/G | 1.6741e-05 | 0.00289314 | intron-variant | UBE3C | GRCh38.p7 | 7:157231365 | ATAGACCTCGGACCA[A/G]AAGATGTTGACATTT | 9690 |
rs772619310 | snp | A/G/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137006 | GAGTGGCGCGATCTC[A/G/T]GCTCACTGCAAGCTC | 9690 |
rs772621686 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242807 | CAAGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 9690 |
rs772644259 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169673 | AAGCCACTGCGCCTG[A/G]CCTGTTTTTGTTTTG | 9690 |
rs772652474 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221514 | TTAGGAGGCCGAGGT[A/G]GGCGGATCATCAGGT | 9690 |
rs772653326 | snp | C/G/T | 5.29227e-05 | 0.00514379 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157187004 | GGTGCAGCACCGCAT[C/G/T]ATGGTACCCAAAGTC | 9690 |
rs772663573 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157214982 | TCAAGGGTCAAGGAA[G/T]AGCTGACTCCAGTTT | 9690 |
rs772709485 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234055 | TTAAGTCCCTGCAAT[A/G]CAATGAATTATGAAA | 9690 |
rs772709529 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239328 | TAACATTGAGTTGAA[G/T]AATCCAGACACACAA | 9690 |
rs772717536 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208121 | GATGTGTCTCCCAGG[C/T]TGGAGTGCAATGACA | 9690 |
rs772735703 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231065 | CCTCCTCACCCTCCC[A/T]TTTTTTTTTAACAGA | 9690 |
rs772740518 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158149 | CTCCTGCCTCAGCCT[C/T]CCAAAGTGATGGAAT | 9690 |
rs772787099 | snp | C/T | 3.30093e-05 | 0.00406246 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267699 | TATGACGAGACACTT[C/T]TGCGAAGTAAACTTC | 9690 |
rs772796809 | snp | C/T | 4.62364e-05 | 0.00480791 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139323 | CAAGGTGTCCCTTGG[C/T]GGCGCGAGCAGGAAG | 9690 |
rs772805244 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208954 | TACCAGCGACCTCTC[A/G]CACACTAATGTTCAG | 9690 |
rs772824071 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251752 | GATCTGAAATTTAGC[A/G]CTTATGTGACATGAT | 9690 |
rs772869699 | snp | C/T | 1.68943e-05 | 0.00290635 | intron-variant | UBE3C | GRCh38.p7 | 7:157181507 | TTTTAAATATGTGTT[C/T]TTCCTTTTAGGGTAT | 9690 |
rs772872556 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258106 | GCATGTACCACCATG[C/T]CTGGCTGACATTTTG | 9690 |
rs772881336 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174342 | TTTCTGATATTTGCA[A/G]GTGAACTATTTTTGT | 9690 |
rs772888764 | snp | A/G | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178807 | TGCTAGCTATGTGGT[A/G]TCAGTGATTGAACAA | 9690 |
rs772898139 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224463 | CCTCCCAAAGTGCTG[A/G]AATTACAGGCATGAG | 9690 |
rs772899565 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201537 | TACACCTTTGGGAGC[C/T]GTGTCTCGGTGTCTC | 9690 |
rs772907241 | in-del | -/TTAG | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269204 | ATGTTCTATATCTTA[-/TTAG]TTAATTTGTATATTT | 9690 |
rs772924005 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203897 | CAAGACACCCAGCTT[A/G]CTGAGGCCTCACAGC | 9690 |
rs772933838 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151171 | CGTCTGTGGACATAA[G/T]CCTGAAGCCACCGTA | 9690 |
rs772999245 | snp | A/G/T | 3.46478e-05 | 0.00416208 | intron-variant | UBE3C | GRCh38.p7 | 7:157182373 | ACACACATATGGGTA[A/G/T]CATTGGCAGATGAGT | 9690 |
rs773015176 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211419 | TTGTTTTTGTTTTTT[G/T]ACTACTAAAGTGGAT | 9690 |
rs773055998 | snp | A/G | 1.67913e-05 | 0.00289748 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186926 | CCTGCTCAACCTGGT[A/G]TGGAGGGACTCTGCG | 9690 |
rs773056747 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157140708 | GCGCCGCGCGGCCTC[C/T]GTTGCAGGCAGGAAC | 9690 |
rs773075963 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149079 | TTTGTTTTTTGAGAT[A/G]GAGTTTTGCTCTTGT | 9690 |
rs773079743 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254061 | CAGGCAGATCCGCCA[G/T]CACTGCCTGGCTTTC | 9690 |
rs773082996 | snp | A/T | 1.70615e-05 | 0.00292069 | intron-variant | UBE3C | GRCh38.p7 | 7:157174879 | AGCAAACTATTAAAT[A/T]TTCATTGAGAGTTGT | 9690 |
rs773149361 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156708 | GTGTAAATTCCCTTC[-/T]TTTTTAAAAAAAAAA | 9690 |
rs773168604 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147802 | GTTAATGTTATGTGA[-/T]TTTTCCTTCTGCAGC | 9690 |
rs773172443 | snp | G/T | 1.66407e-05 | 0.00288446 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170415 | GTAAGGCAGCTTCTG[G/T]TTTTTTACAAACAAA | 9690 |
rs773175958 | snp | C/G | 3.29658e-05 | 0.00405978 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207739 | CAATGATGCCTTTTA[C/G]TTTAGAAGAGCTGAT | 9690 |
rs773183534 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191521 | GTCTCGAACACCTGG[A/G]CCCAAGTAATCTGCT | 9690 |
rs773194184 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249852 | GATTTGCTTCAAATA[C/T]ACTCTGTGCATCCAT | 9690 |
rs773204112 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157225038 | TTTTATTTTTGAGAC[-/AG]AGATTCACTCTGTCA | 9690 |
rs773215115 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229471 | AGGCATGCACCACCA[C/T]GCCCGGCTAATTTTT | 9690 |
rs773215668 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189855 | GCCCAGGCTGGAGTG[C/T]AGTGGTGTGAACTCG | 9690 |
rs773217101 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239861 | ACACTGGGTGCAGCT[C/G]CATGAGCTGGGGAGC | 9690 |
rs773253095 | snp | C/G | 3.32602e-05 | 0.00407786 | intron-variant | UBE3C | GRCh38.p7 | 7:157223226 | GAAAGTACAAGTGAA[C/G]TAATTAAGGTTTTAA | 9690 |
rs773261205 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218490 | ACAGAAATATTCGAG[A/G]AGAGAAAACAGGAGT | 9690 |
rs773264239 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157176694 | CTTTTAATGGTCTGC[G/T]TATAGGTAGAGAGCA | 9690 |
rs773281850 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206612 | AAACTTCTTTGAAAC[-/AG]AGTCTGGCTCTGTTC | 9690 |
rs773338745 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157190577 | AAGGTGCTGGTGGGC[A/G]GTGCTGCCCAGGGTT | 9690 |
rs773352760 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182114 | CTTTTTCAGGCAACA[A/G]GTTTTTACAGCCTTC | 9690 |
rs773358388 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205159 | TAGCAGAAAGAATGG[G/T]CAGCAGAGAACTAAG | 9690 |
rs773376083 | snp | G/T | 1.65732e-05 | 0.00287859 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254255 | TTAGGTATTAATTTC[G/T]GGTGCACAAGTTCCC | 9690 |
rs773438050 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218557 | ATAAGATATTTGTGA[A/G]TTAAGCCTGTTGCAT | 9690 |
rs773470219 | snp | A/G | 3.2994e-05 | 0.00406152 | synonymous-codon, intron-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157169056 | TGTTTAGGAAGAAAG[A/G]CGAAGGTTGAAAAAT | 9690 |
rs773488763 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237833 | GGAAGAACACTTAAG[C/T]CCAGGAGTTCAAGAC | 9690 |
rs773519555 | snp | A/G/T | 0.000230607 | 0.0107359 | intron-variant | UBE3C | GRCh38.p7 | 7:157223129 | GGCGGGGATGTGTTC[A/G/T]TGGAACTGGATTTAG | 9690 |
rs773548199 | in-del | -/TAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199865 | GTCTCCTTTAACTTG[-/TAT]TATTACCATTTTTTC | 9690 |
rs773551822 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264239 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs773557018 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147111 | TGTGCTGAATTGGTA[C/G]ATCAAGTTGGGAAAA | 9690 |
rs773590942 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259405 | TGTCGCAGCCCCACC[A/G]TTGGGAGTGTACAGA | 9690 |
rs773601228 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185878 | GTGTTTTGTTTGGTA[A/G]GTTATTATAAATTAT | 9690 |
rs773602693 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177034 | CATATTTTTTAATGC[C/T]GTTGAACATTTCTGA | 9690 |
rs773640633 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178864 | TAAGTAGTAGGCAGG[A/T]TCAGAACTGTGGCTC | 9690 |
rs773646741 | in-del | -/ATACTAT | 1.80471e-05 | 0.00300387 | intron-variant | UBE3C | GRCh38.p7 | 7:157170263 | GAATTGTGTGTCCAA[-/ATACTAT]ATTTATGGGTCATTT | 9690 |
rs773648227 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156803 | CTCTCGGAGACAGTT[C/T]CTGATCAGTAGATAG | 9690 |
rs773664056 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203939 | TACCTAAAACGTGCT[C/G]AAAATATGTGCATTA | 9690 |
rs773674447 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178795 | TGTTTTACAAGATGC[C/T]AGCTATGTGGTGTCA | 9690 |
rs773696802 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157262903 | GAATGGGACATTGCT[C/G]TAGTTTGATTCACAT | 9690 |
rs773723165 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247703 | TCTCCAAAAAAAAAA[-/AG]AGCATAAGTAATATT | 9690 |
rs773734597 | in-del | -/T | 1.68221e-05 | 0.00290014 | intron-variant | UBE3C | GRCh38.p7 | 7:157182346 | ATGAAATACAAGATC[-/T]TTTTTACCTGAACAC | 9690 |
rs773736200 | snp | A/G | 0.00016288 | 0.00902293 | intron-variant | UBE3C | GRCh38.p7 | 7:157164425 | TTCCCAAAGTGTTGG[A/G]ATTACAGGCGTGAAC | 9690 |
rs773739525 | snp | C/T | 2.79279e-05 | 0.00373673 | intron-variant | UBE3C | GRCh38.p7 | 7:157207968 | TTTTTTGTTTACTGA[C/T]ATTGAAAAATGTACA | 9690 |
rs773741197 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248420 | CAGGCTTCTTTCTTT[C/T]CAAGTTGCTTGGAAC | 9690 |
rs773760532 | snp | A/C | 6.66756e-05 | 0.0057735 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186919 | CCAACACCCTGCTCA[A/C]CCTGGTGTGGAGGGA | 9690 |
rs773763418 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201747 | GTTTAGCCTTTAATG[C/T]CAGGTTTCTGAGACA | 9690 |
rs773782430 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209721 | AATTTCCATGACAGG[C/T]TTATCTTTAGTATGT | 9690 |
rs773784965 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251624 | TTATGGATTCCAAGT[C/G]AAAATAGACTTTCTG | 9690 |
rs773792675 | snp | G/T | 3.3484e-05 | 0.00409156 | intron-variant | UBE3C | GRCh38.p7 | 7:157231368 | GACCTCGGACCAAAA[G/T]ATGTTGACATTTTAT | 9690 |
rs773802940 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215090 | TGCCACAAGAGAATC[A/G]CCACTTCTAAATTGG | 9690 |
rs773803111 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202296 | ATAGGTAGGAATTTC[A/G]TACTTAAAATCCTTC | 9690 |
rs773809177 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172613 | GAGAAGGAACTGAGA[A/G]CCAGTCTAGAGAGGC | 9690 |
rs773851436 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217698 | AAAAATCAGCCGGGC[A/G]TGGTGGCAGACGCCT | 9690 |
rs773868155 | snp | A/C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165277 | TTTGACCTTTGCGTC[A/C/G]TTTCCCATATTTCCC | 9690 |
rs773878846 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267958 | GGACATTGCTTTTCA[A/G]ATAACTTAAAATAAC | 9690 |
rs773884755 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230110 | GATGGGGTTTCACCA[G/T]GTTGGCCAGGCTGGT | 9690 |
rs773901809 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151093 | GTCATGGTGTATTTG[C/T]CCAGCCCACTCTCGG | 9690 |
rs773910022 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152594 | TGAGCTCATTGATCT[C/T]GACTTCTGATATGTG | 9690 |
rs773926786 | snp | G/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256947 | ATCCTGTTATTAAGG[G/T]CTTCTGGAGAGTTGT | 9690 |
rs773931075 | in-del | -/G | 1.64765e-05 | 0.00287019 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182280 | AGAAAGAGTGGTGGA[-/G]CACCCTGGCTTTTCT | 9690 |
rs773936673 | snp | A/G | 3.41364e-05 | 0.00413123 | intron-variant | UBE3C | GRCh38.p7 | 7:157178680 | GTGAATACTTTTTTC[A/G]TTTTTACAGGTTGCT | 9690 |
rs773944516 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194837 | TAAGTGATGACTTCA[A/G]TATTAGCTGAGGATA | 9690 |
rs773975371 | in-del | -/TGTT | 8.25689e-05 | 0.00642477 | intron-variant | UBE3C | GRCh38.p7 | 7:157163797 | ACCTCCTTTTTTCTC[-/TGTT]TGGGTGTAGGAGGAA | 9690 |
rs774026122 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211058 | CTGTTTTGAGATGTC[C/T]GTGTGCATCCACCAA | 9690 |
rs774064753 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186282 | TACAAAAATTAGCTG[A/G]GTGTGGAGGCGGGCA | 9690 |
rs774100353 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172746 | ACGGCAGATAATCGG[A/G]CTTGCTTTCTGGAAC | 9690 |
rs774136541 | snp | C/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207414 | TCTATGGTACCGTTG[C/G]TTCAGGTGATATCCA | 9690 |
rs774153646 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222565 | GCTGGGACTATAGGC[A/G]CGTGCCACCATGCCC | 9690 |
rs774162874 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157149985 | CATAGCCCATCACCT[C/T]CGATGGTGGTCAAAT | 9690 |
rs774191811 | snp | A/C | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157225432 | GGTTGATTTATGCAG[A/C]TAAGCAAGAAGTTCA | 9690 |
rs774192468 | snp | A/G | 1.6623e-05 | 0.00288292 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216877 | TTCAGGTTATCACCA[A/G]TCTAGTGAAAATGTT | 9690 |
rs774233777 | snp | C/T | 8.61067e-05 | 0.00656094 | intron-variant | UBE3C | GRCh38.p7 | 7:157182367 | ACCTGAACACACATA[C/T]GGGTAGCATTGGCAG | 9690 |
rs774265672 | snp | A/G | 4.50075e-05 | 0.0047436 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139305 | CGACTTCAAGACGCG[A/G]CCCAAGGTGTCCCTT | 9690 |
rs774289951 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164064 | GGCAGTTTCCAGACT[A/G]GAGAAGGAACATGGG | 9690 |
rs774313585 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246145 | GGACGAGTCCTTAAA[A/G]TGTGAATCTCAAGGG | 9690 |
rs774323822 | snp | A/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182273 | ATGTTCAAGAAAGAG[A/T]GGTGGAGCACCCTGG | 9690 |
rs774348052 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161819 | TCTCATGTCTGTAAT[C/G]CCAGCAGTTCGGGAG | 9690 |
rs774360242 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204185 | TGTCTCATATTTCCT[A/T]CTGGGAATAAAGTTT | 9690 |
rs774365547 | in-del | -/GA | 1.72579e-05 | 0.00293746 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267759 | AGCTGAGCTGAAGCT[-/GA]GATGCTGGGGTCAGA | 9690 |
rs774377779 | snp | C/T | 4.94752e-05 | 0.00497344 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254037 | CTTGGTGGCAGACTA[C/T]AGGCTGAACAGGCAG | 9690 |
rs774402642 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157380 | TCATGAAAATGATTA[-/T]TTTGTAGAACAAGAT | 9690 |
rs774416946 | in-del | -/TTA/TTTA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254403 | AATTAATTTATTTAT[-/TTA/TTTA]TTTTTTTTTTTCAGA | 9690 |
rs774425291 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202432 | GAGGCCGAGGCCAGC[A/G]GATCACCTGAGGTCA | 9690 |
rs774463345 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179148 | ATCCAAGATTGGTGT[C/T]TGCAGTGCAGCTGCC | 9690 |
rs774491472 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188580 | TGCTGGATTTCAATG[C/T]ATCACTGCCCTGGGC | 9690 |
rs774507098 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238941 | GGTATTGTGTGATGG[C/T]ACTGTTAGACCAAGT | 9690 |
rs774513779 | snp | C/G | 0.000325203 | 0.0127474 | intron-variant | UBE3C | GRCh38.p7 | 7:157164393 | AACTATGGCCTCATG[C/G]AATCGCCTCCCTCAT | 9690 |
rs774540402 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175690 | CAGAACTAGTCTTTA[A/T]TAACTGATTTTTCCA | 9690 |
rs774547953 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232251 | TCATTTCCAAAGAAG[G/T]TTATATTCACAGATT | 9690 |
rs774592952 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199702 | TCTCGAACTCCTGAC[C/G]TCAAGTGATCCACCC | 9690 |
rs774598741 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229277 | ATCAGAGCACATCTT[A/T]ACTTGGTCCACCTTG | 9690 |
rs774605378 | snp | A/T | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181645 | ACCATTGCACTTTAC[A/T]TACAACTCCTGTCCG | 9690 |
rs774610733 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263910 | TTTATCTACCTACAT[-/G]GAGTGTGTGTTAATG | 9690 |
rs774616749 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191386 | AACCCCGCCTCCCAG[A/G]CTCAGGTGATCCTCC | 9690 |
rs774622826 | snp | G/T | 1.81678e-05 | 0.00301389 | intron-variant | UBE3C | GRCh38.p7 | 7:157253917 | ACCTATTATCATACT[G/T]TGAGGATTTTGAGAT | 9690 |
rs774636475 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264728 | AGGCATGCACCACTA[C/T]AGCCGGCTAATTTTT | 9690 |
rs774637757 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153885 | GTGGTTTCAGTTACT[C/T]GGGAGGCTGAGGTGG | 9690 |
rs774659017 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227464 | AGCACTTTGGGAGGC[CA/TG]AGGCAGGCAGATCAC | 9690 |
rs774695226 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223926 | ACCTATCTCAAAGGG[A/G]GGAAGAAACTTTGCA | 9690 |
rs774712232 | snp | A/G | 1.65877e-05 | 0.00287986 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170404 | TTACCCTTTTGGTAA[A/G]GCAGCTTCTGTTTTT | 9690 |
rs774726686 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265658 | GACCCATTATCAGAT[A/G]AGAAAAGCACGGCAC | 9690 |
rs774728918 | in-del | -/AAAAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220445 | TATGCACCATCAAAT[-/AAAAC]AATTAGAGATTTCTT | 9690 |
rs774745419 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157884 | TACTTGGAGGCCGAG[A/G]CAGGAGAATTGCTTG | 9690 |
rs774772731 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169936 | TGATCCACCCACCTC[A/G]GCCTCTCAAAGTGCT | 9690 |
rs774787255 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213633 | TGTGTTAAGGTGTTT[C/T]GAGATCACAAAATGG | 9690 |
rs774802131 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242681 | TTTTTATCTTCTAGA[A/G]ATATTTTGGTGAGCA | 9690 |
rs774807227 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223086 | CTGTGCTGATCCTGC[A/G]CTGTGCATGGCTCAT | 9690 |
rs774848981 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170118 | AGCCACCATGCCTGG[-/T]TTTTTTTTTTTTTTT | 9690 |
rs774872139 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146947 | TGAGACACCGCGCCC[A/C]ACCATAGTAAGCATT | 9690 |
rs774875173 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239911 | ATCCCACTGTTGCTG[-/C]TTTCTGGGTGATGCA | 9690 |
rs774884641 | snp | A/T | 1.68912e-05 | 0.00290608 | intron-variant | UBE3C | GRCh38.p7 | 7:157223219 | TGCAGGGGAAAGTAC[A/T]AGTGAACTAATTAAG | 9690 |
rs774923493 | snp | A/C | 1.6501e-05 | 0.00287232 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157175012 | TTATTTCAGATAAAA[A/C]GATTGATGAGCCTCT | 9690 |
rs774985561 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216599 | CCAAATTTGTGTTTC[A/G]AAGCTTAATCGCCAC | 9690 |
rs775003249 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141508 | CGTTGCCCCTATGCT[-/AC]ACACCTGGACAGCGT | 9690 |
rs775012941 | snp | A/G | 3.41711e-05 | 0.00413333 | intron-variant | UBE3C | GRCh38.p7 | 7:157174876 | ATTAGCAAACTATTA[A/G]ATTTTCATTGAGAGT | 9690 |
rs775013451 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184028 | ACAAGCCCTCAAGCC[C/T]GGTAAGCCCCGTGCC | 9690 |
rs775015797 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260462 | AATCTCTCGAGCGCA[A/G]GGAAAGCTGGGTGCT | 9690 |
rs775044276 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187563 | ATTTTTTGTTTTTGT[A/G]TGTGTGTGTGTTTGT | 9690 |
rs775071812 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205456 | AGTACAAGGATTCTT[A/G]TCGGGGATAACAGTG | 9690 |
rs775087045 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177376 | GGATATCCTTTTCCC[A/G]TCCAAGGCTGTCCCG | 9690 |
rs775127130 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160440 | GGATGCCTTCTGTTT[A/G]TGACCAGTGATGCTG | 9690 |
rs775136739 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154523 | TTAGTGATTCCATAT[C/T]GGCATCTTTATATTT | 9690 |
rs775137807 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178010 | ATCTAAAAATAAGTT[A/C]GGTGTTAGACAAAGT | 9690 |
rs775178450 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249160 | TTAGTATATTCGTAG[A/G]GGTGTGCAGCCATCA | 9690 |
rs775183604 | in-del | -/CTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182794 | CGCTCTGTCACTAGG[-/CTC]CTGGAGTGCAGTGGC | 9690 |
rs775193610 | snp | A/G | 2.1972e-05 | 0.00331444 | intron-variant | UBE3C | GRCh38.p7 | 7:157207945 | TTTAAGGTATAGAGT[A/G]TATGTATTTTTTTGT | 9690 |
rs775199365 | in-del | -/ACAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157182681 | TATGTTTGAAAACAT[-/ACAT]ACATACATACATGCA | 9690 |
rs775264756 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250297 | CATCTCGGTTCACTG[C/T]ACCCTCAGCCTCCTG | 9690 |
rs775354320 | snp | A/C/G | 6.60353e-05 | 0.00574577 | intron-variant | UBE3C | GRCh38.p7 | 7:157256898 | TTTCATAAAGCATGT[A/C/G]TTCATTTTGCCATAG | 9690 |
rs775428461 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209252 | CCTGGTTTTACAACA[C/T]ATTTCTCTTAGGAGC | 9690 |
rs775430326 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201794 | TCTTCCATGTCAACA[C/T]GGATGATCACAGGGT | 9690 |
rs775439302 | snp | A/G | 3.29565e-05 | 0.00405921 | intron-variant | UBE3C | GRCh38.p7 | 7:157267535 | TGTATTAAAACTCAT[A/G]TAATGCCATGCTTGT | 9690 |
rs775456741 | snp | C/T | 3.30316e-05 | 0.00406383 | intron-variant | UBE3C | GRCh38.p7 | 7:157225395 | AACCTTACAGCTTTC[C/T]TTGTTTGTTAGATCT | 9690 |
rs775458041 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165706 | GCTGCCTAATTGTTA[A/T]ATACATCCATTGACT | 9690 |
rs775458412 | snp | A/G | 1.75758e-05 | 0.00296438 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170305 | TGTTTTTCTTCCAGT[A/G]TTCCATCCAAAGAAG | 9690 |
rs775488721 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244711 | GCATTAATTGCGTCG[C/T]GACTGCACTCACTTA | 9690 |
rs775508364 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258409 | TCTCAAGGGGGAAAA[A/G]GTAATGTTAAGGTTT | 9690 |
rs775510002 | snp | C/T | 1.73601e-05 | 0.00294614 | intron-variant | UBE3C | GRCh38.p7 | 7:157223387 | ATTGTCACTACGTAT[C/T]ATATTAGTGTTAAGA | 9690 |
rs775536037 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157831 | AAAAACAGCACAAAA[A/C]TTAGCCAGGCATGGT | 9690 |
rs775550761 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238200 | CTAAACTTAAAATCA[C/G]CTTTGAGAGGCGGCA | 9690 |
rs775570038 | snp | A/G | 1.65674e-05 | 0.00287809 | intron-variant | UBE3C | GRCh38.p7 | 7:157248627 | GTATAGCAAGTAGCA[A/G]CATCTCCTTGTGTGT | 9690 |
rs775578235 | snp | A/C | 4.9666e-05 | 0.00498302 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170387 | TGCTAATGGCCCCAA[A/C]CTTACCCTTTTGGTA | 9690 |
rs775589422 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179706 | GAATTATAAGCAGCT[A/G]TGCTTTCCTTCACCT | 9690 |
rs775602182 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255142 | GATAAATATATACAT[A/T]CACAACGTACATGGG | 9690 |
rs775602256 | in-del | -/CTCCAGC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235156 | GGCCTTACCATTGCA[-/CTCCAGC]CTGGCAACAAGAGCA | 9690 |
rs775622957 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248510 | TGCTCTTTCTGAAGA[C/G]CTACGAAGACGATGT | 9690 |
rs775662376 | snp | A/G | 5.03292e-05 | 0.00501618 | intron-variant | UBE3C | GRCh38.p7 | 7:157182343 | GGTATGAAATACAAG[A/G]TCTTTTTTACCTGAA | 9690 |
rs775669972 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234343 | CCTTTTTGAGTTAAT[C/T]TTTGTAGATTGTATG | 9690 |
rs775681681 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184890 | GAAAGGAACAGAAGA[C/T]ATTCACTGCCAGGGC | 9690 |
rs775686877 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247175 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTGACT | 9690 |
rs775695568 | snp | C/T | 1.66657e-05 | 0.00288662 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267719 | AAGTAAACTTCTCTA[C/T]GCGATTGAATGTGCC | 9690 |
rs775725040 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249579 | TGGCCTCCTGAAGTG[C/G]TGGGATTACAGGCGT | 9690 |
rs775729273 | snp | C/G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202384 | TAAGCCGGCCGGGCG[C/G/T]GGTGGCTCACGCCTG | 9690 |
rs775734860 | in-del | -/CTGCCTCCCAGGTTCAAGTGATTCTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160159 | GGCTCACTGCAACTT[-/CTGCCTCCCAGGTTCAAGTGATTCTC]CTGCCTCAGGCCTCC | 9690 |
rs775736045 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174614 | TGTGCCACCACGCTC[A/G]GCTAATTTTTGTATT | 9690 |
rs775744014 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181877 | TAACATGGTTATTTT[C/G]CTGCTTTTCTAAGTA | 9690 |
rs775748684 | snp | C/T | 4.35341e-05 | 0.00466531 | intron-variant | UBE3C | GRCh38.p7 | 7:157187037 | GCAAGTGTCCGTGGG[C/T]GTCTGTGCCAGGGGG | 9690 |
rs775846988 | snp | A/G | 3.41857e-05 | 0.00413421 | intron-variant | UBE3C | GRCh38.p7 | 7:157220809 | CAGGGTTACTGAGGT[A/G]TGAATTACATGCTGT | 9690 |
rs775847203 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189313 | TTTTCTGAGAGGAAA[C/T]TTTAGATATATTACC | 9690 |
rs775891834 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157156624 | TTCTTTAATCCTTAC[A/G]TTCACACTCTATTTT | 9690 |
rs775896885 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267776 | ATGCTGGGGTCAGAC[C/G]CCTACAGAGAACCAG | 9690 |
rs775912864 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207403 | TTAATTCAAGGTCTA[C/T]GGTACCGTTGCTTCA | 9690 |
rs775922308 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222977 | GTGCTAGGGCTAGCT[C/G]TGCACTTGAGACGTG | 9690 |
rs775960868 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195716 | TTAGATGGCTTTAGT[G/T]TGAGATTTGAGACTT | 9690 |
rs775973940 | in-del | -/ATC | 5.18623e-05 | 0.005092 | intron-variant | UBE3C | GRCh38.p7 | 7:157223385 | TTATTGTCACTACGT[-/ATC]ATATTAGTGTTAAGA | 9690 |
rs775984348 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150274 | ATCCCAGCTACTTGG[A/G]AGGCAGAGGCGGGAG | 9690 |
rs775986025 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174823 | TAGGTTTGATTAAAT[A/G]TGCATTGCCACTAAA | 9690 |
rs776018580 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209876 | ACTTTATTCATCATT[G/T]AAAGTTTTAAGAGTT | 9690 |
rs776028891 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234776 | GATTTGATGTTGATT[A/T]GTGAGTTGGCTTTGG | 9690 |
rs776039379 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172869 | CTCTCCAGAGCACCT[A/G]TTGCCTTTGAGTGAG | 9690 |
rs776042330 | snp | A/G | 2.01998e-05 | 0.00317797 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186966 | GTCTTCACCACCATG[A/G]CCTCCGTCTGCCACA | 9690 |
rs776051970 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157243560 | TTAGAGTGAGGCCCA[C/T]GGCCTGGCCCCTCCC | 9690 |
rs776061805 | in-del | -/T | 3.3042e-05 | 0.00406447 | intron-variant | UBE3C | GRCh38.p7 | 7:157257091 | CCACTTCATAATAAG[-/T]AAAGGCAGCAGAACA | 9690 |
rs776074017 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194789 | AAAGCTAAGCTGAAT[C/T]GTGTCCTGCAGTTAT | 9690 |
rs776094182 | in-del | -/TTGT/TTT/TTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242514 | ACTGAGCCTGAGTTG[-/TTGT/TTT/TTTTTT]TTTTTTTTTTTTTTT | 9690 |
rs776105656 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, intron-variant | UBE3C | GRCh38.p7 | 7:157220737 | GTGTGGAGGTTCCGG[C/T]GGATGGGGAGGATAG | 9690 |
rs776121867 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207759 | GAAGAGCTGATAATG[G/T]TGTCTCGATGCCTTC | 9690 |
rs776176030 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148020 | ATGTCTTTGTCTGGT[C/T]TGGTATTAGGGTGAT | 9690 |
rs776199238 | in-del | -/TTTA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208607 | AAATATTTCTTAGAT[-/TTTA]TTGTTTTTTCAAACC | 9690 |
rs776199343 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196000 | GTAATTAAGGTTACT[A/G]TGGATTTCAAGACGA | 9690 |
rs776215139 | snp | C/T | 3.29783e-05 | 0.00406055 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231082 | TTTTTTTTAACAGAG[C/T]CTGATTTGAAAAAGC | 9690 |
rs776237728 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264633 | ATTGCCCAGGCTGGA[A/G]TGCAATGCGTGATCT | 9690 |
rs776278720 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165027 | TGTTTAGCAACACCC[A/G]TGGCCTCTACCCACT | 9690 |
rs776289737 | snp | A/G | 1.65067e-05 | 0.00287282 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231254 | GGCTTCTGTACCCCA[A/G]CCCGGCTGCTCAGAT | 9690 |
rs776315421 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145992 | AAGTCATTACCAAAG[C/T]CAAGGTAACCTAGAT | 9690 |
rs776322102 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259594 | GTATGAACATTGAAA[A/G]CACTGTGCTAAGTGA | 9690 |
rs776322804 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187288 | AATGTGAGTTTATTC[A/G]CCCATCTGAAAGGCT | 9690 |
rs776334295 | snp | G/T | 8.28137e-05 | 0.00643428 | intron-variant | UBE3C | GRCh38.p7 | 7:157163899 | CTCTGTAGATAAGCA[G/T]TTTTTCTACAGCATT | 9690 |
rs776350429 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206542 | GCTGGGATTACAGGC[A/G]TGAGCCACCATACCC | 9690 |
rs776395407 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152586 | TTCGTTTATGAGCTC[A/G]TTGATCTCGACTTCT | 9690 |
rs776400963 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189694 | CTTCTTTCATAGATA[C/G]CATATTCATGTGATT | 9690 |
rs776407254 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226280 | GCTCCAATGACACTG[C/T]CGTTAGTAAAGGAGA | 9690 |
rs776413330 | snp | A/T | 3.60114e-05 | 0.00424316 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267805 | AGTGCTTCCTTCGTC[A/T]GCAGCGCCTCCCCAG | 9690 |
rs776421134 | snp | C/T | 3.31115e-05 | 0.00406874 | intron-variant | UBE3C | GRCh38.p7 | 7:157163786 | ATTATAACCTTACCT[C/T]CTTTTTTCTCTGTTT | 9690 |
rs776448882 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153711 | TGGCCTTTTTAAAAA[G/T]TTAACTTTTCCTCCC | 9690 |
rs776448897 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252675 | TCTTTCTGTAAATGG[C/T]AAGAGACTGGGACAT | 9690 |
rs776509878 | snp | A/G | 3.29658e-05 | 0.00405978 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174993 | ATCTGAGAGACTTAC[A/G]TGCTTATTTCAGATA | 9690 |
rs776511915 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228109 | ATTCCACGTGTCATC[C/T]AGTCATTGAAGTGAA | 9690 |
rs776519809 | snp | A/C | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184019 | AAGAAGCCGACAAGC[A/C]CTCAAGCCCGGTAAG | 9690 |
rs776536173 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242838 | AAGGCGGGAGAATCA[C/T]GAGGTCAGGAGTTCT | 9690 |
rs776550759 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183321 | AATGGGGGTTCCTCA[G/T]CCCCTCCTTGGGATT | 9690 |
rs776557021 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155882 | TGCACGCTGTCAGGA[C/G]GATGGCCTCGGTCGT | 9690 |
rs776568001 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144032 | ACAGTGAGTCCACTG[A/G]CTGCGGAGCTGGGAA | 9690 |
rs776572627 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141980 | AGCTGTTGTGCACAC[C/T]GCTGCCACAGTTTCC | 9690 |
rs776592943 | snp | G/T | 1.65228e-05 | 0.00287422 | intron-variant | UBE3C | GRCh38.p7 | 7:157223235 | AGTGAACTAATTAAG[G/T]TTTTAAAATGTGTTT | 9690 |
rs776599395 | snp | A/G | 1.77363e-05 | 0.00297789 | stop-gained, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207919 | TGGAACAGAAAAGAT[A/G]GATTCAGTTATTTAA | 9690 |
rs776603072 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228824 | CAGTAAATTGTATTT[G/T]CCCTATTTGACACAT | 9690 |
rs776605724 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183917 | TGGTGTATTTGCGGG[C/T]GCTGCAGACCTTCCT | 9690 |
rs776630297 | snp | C/G | 1.65042e-05 | 0.0028726 | missense, intron-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157169100 | AGTCATTTATTCGAG[C/G]CTATAGAGACAGAAA | 9690 |
rs776636333 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231733 | CAATGAGAAGACCTC[A/G]CCAGGGGCTGCCTCT | 9690 |
rs776647962 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254264 | AATTTCTGGTGCACA[A/G]GTTCCCATAAGCCTA | 9690 |
rs776663418 | snp | A/G | | | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248508 | TTTGCTCTTTCTGAA[A/G]AGCTACGAAGACGAT | 9690 |
rs776686513 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221225 | AGCTGCTATAAACAT[A/C]TATGTACAGGTTTTT | 9690 |
rs776688360 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219309 | TTGATTTATATTTTG[A/G]CACAAGTCCCTTATC | 9690 |
rs776693985 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201760 | TGCCAGGTTTCTGAG[A/G]CATCTTTGGTTTCTA | 9690 |
rs776699213 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209095 | ATTGCTAATGGAACT[G/T]TCTTCTTGGCCATGT | 9690 |
rs776699234 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198056 | TGAAGCTCCAGGGGG[-/A]ATCTCTCCTCTTTTA | 9690 |
rs776725329 | snp | A/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170380 | TTCCCATTGCTAATG[A/G]CCCCAACCTTACCCT | 9690 |
rs776726267 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221985 | AGCGATCTTCCTGCC[A/G]TAGCTTCCAAAGTAG | 9690 |
rs776739506 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218890 | ACAAAACCCTTCGTC[A/G]TCATATTTGTAGGAT | 9690 |
rs776756590 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216502 | TCTGCCCTCTCCCTC[C/T]TCCCACCCTCCCCCT | 9690 |
rs776788171 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212257 | ACCAGATTTTACATA[C/T]CACATTTAAGATAAA | 9690 |
rs776789559 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172830 | AGCACAGACAGGCAG[G/T]TGCTGTGAGATGTCG | 9690 |
rs776812056 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157222926 | GCCAGGGCACCGCCC[A/G]CTGCTGGATCTGGCT | 9690 |
rs776821905 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257280 | ACACATTGTGGTTAT[A/G]ATTGCCTGTGAACAA | 9690 |
rs776829553 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194419 | TATTCCAAATCTAGT[A/G]GCATATTCAGGTCAT | 9690 |
rs776891961 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211280 | TTAAAAAGTAATAAA[A/G]CAACAGCAGTGCCCT | 9690 |
rs776945911 | in-del | -/A | 8.59143e-05 | 0.00655361 | intron-variant | UBE3C | GRCh38.p7 | 7:157220815 | ACTGAGGTATGAATT[-/A]ACATGCTGTCAAATT | 9690 |
rs776945994 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | UBE3C | GRCh38.p7 | 7:157248600 | GGGGTCAGGAGGAGG[A/G]TTCACATACCTGTAT | 9690 |
rs776968248 | in-del | -/TGTT | 1.64833e-05 | 0.00287078 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174956 | TTAAACACAGCTCTC[-/TGTT]TGTCAAGCAGTTGGA | 9690 |
rs776989281 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157246370 | GCAGAAGCACAGTCC[C/T]GGCTCTCTGGAAGCT | 9690 |
rs776999014 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240555 | TGGGTCTGACTAGGA[C/T]GTAGAGTCAGATTTA | 9690 |
rs777004543 | in-del | -/AGCATACTGGTCACTCAGA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177272 | CGGGTGTTTCTCAGG[-/AGCATACTGGTCACTCAGA]TGGCTCTTTTTCAAG | 9690 |
rs777011881 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145333 | GACCAGCCTGGTCAA[C/T]ATGGTGATACTCTAT | 9690 |
rs777013388 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195980 | GTAAAAGAGATTTTG[C/T]AGATGTAATTAAGGT | 9690 |
rs777021421 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266761 | ATTTTTATAGACAGG[G/T]TCTCACTGTGTGTTG | 9690 |
rs777036245 | snp | A/G | 1.72314e-05 | 0.0029352 | intron-variant | UBE3C | GRCh38.p7 | 7:157223381 | TTCTTTATTGTCACT[A/G]CGTATCATATTAGTG | 9690 |
rs777070517 | in-del | -/AT | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138113 | GTGGATATAAGACAC[-/AT]GTTTATGTATAGGTG | 9690 |
rs777120853 | in-del | -/G | 1.65551e-05 | 0.00287702 | intron-variant | UBE3C | GRCh38.p7 | 7:157184052 | CCGTGCCCTGCATCT[-/G]GGGGGCTGCGATGCA | 9690 |
rs777140677 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216383 | TATTTTAGGTTTGGG[G/T]GTACATGTGAAGTTT | 9690 |
rs777144372 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194912 | GATTATGGTAAAATA[C/T]GGAAGGAGGTAGATA | 9690 |
rs777147947 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144115 | AGCATAGCACATTGG[A/G]GAGTGAATGGGAAGT | 9690 |
rs777204810 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153492 | ACAGAGTCCAGGTCT[C/T]ACGGCGTTGCCCAGG | 9690 |
rs777210872 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165696 | GAGCCACCCTGCTGC[C/T]TAATTGTTAAATACA | 9690 |
rs777222555 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216908 | GAAGTCCAGAGACAC[A/G]AGGAGAAATTTTTGT | 9690 |
rs777287148 | snp | C/T | 2.97287e-05 | 0.00385532 | intron-variant | UBE3C | GRCh38.p7 | 7:157223180 | GATTTCAAGAATCTT[C/T]ACCTTAAGAATTGTC | 9690 |
rs777288768 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157253719 | GTGCTTCGGAGGAAA[C/G]ATGGATGGTTAGTGA | 9690 |
rs777290907 | snp | G/T | 1.79258e-05 | 0.00299376 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267799 | AGAACCAGTGCTTCC[G/T]TCGTCAGCAGCGCCT | 9690 |
rs777307064 | in-del | -/AGA | 4.56965e-05 | 0.00477977 | intron-variant | UBE3C | GRCh38.p7 | 7:157217038 | TGTGTCTTTCTGGAG[-/AGA]AGAATTAAGCACTTT | 9690 |
rs777312134 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266713 | AATAGCTTGTACAGG[-/A]AAGATAGAATAAATC | 9690 |
rs777340553 | snp | A/G | 1.65455e-05 | 0.00287619 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254129 | TCCGAATGTTTGATC[A/G]GCAAGAAATTCAGGT | 9690 |
rs777343218 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229883 | TTCCCAAAGTGCTGG[G/T]ATTACAGAAGTGAGC | 9690 |
rs777350710 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181615 | AGCAAAAATTTTGCT[A/G]GAGAATGTTCTAAAA | 9690 |
rs777371276 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157184005 | TGAGGAGGAGAGTGA[A/G]GAAGCCGACAAGCCC | 9690 |
rs777386317 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191095 | TTTAAATACATAAAT[C/T]ATAAGACACCTAGTT | 9690 |
rs777392942 | in-del | -/A | 1.65762e-05 | 0.00287886 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254281 | TTCCCATAAGCCTAG[-/A]GGACCTAAAATCCTT | 9690 |
rs777447097 | snp | A/G | 1.75585e-05 | 0.00296293 | intron-variant | UBE3C | GRCh38.p7 | 7:157188964 | GGTGTACAAATGAAT[A/G]TGGAGACCTTTGTAC | 9690 |
rs777472698 | snp | A/C | 1.65814e-05 | 0.00287931 | intron-variant | UBE3C | GRCh38.p7 | 7:157169001 | CAAAATGTCATTTTC[A/C]CTGGATTCTGACCAA | 9690 |
rs777475803 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157215703 | GACTTTTTCAGAAAA[C/T]GCCGTCTTGAGCTCT | 9690 |
rs777483496 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171188 | TGGAGTGCAGTGGTG[C/G]ATTCTTGGCTCACTG | 9690 |
rs777534996 | snp | C/T | 3.81993e-05 | 0.00437015 | intron-variant | UBE3C | GRCh38.p7 | 7:157187031 | AGTCAGGCAAGTGTC[C/T]GTGGGCGTCTGTGCC | 9690 |
rs777550110 | snp | C/T | 1.71018e-05 | 0.00292414 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207904 | AACAATGCATACAGA[C/T]GGAACAGAAAAGATG | 9690 |
rs777577849 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232235 | GTTATCTGCAAATAC[C/G]TCATTTCCAAAGAAG | 9690 |
rs777609197 | in-del | -/AAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261307 | GCAAAACTCTGTCTG[-/AAA]AAAAAAAAAAAAAAA | 9690 |
rs777630092 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228685 | AGGTGGCGGGCACGG[C/G]AGGGCAGCACTGCAT | 9690 |
rs777643309 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146593 | TCCCTTTTGTCAATA[C/T]CATACCATCTTGATT | 9690 |
rs777643560 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247122 | AACTCCTGACCTCAG[A/G]TGATCCAGCCGCCTC | 9690 |
rs777674720 | snp | A/G | 3.32287e-05 | 0.00407593 | intron-variant | UBE3C | GRCh38.p7 | 7:157231330 | AATGCTTGGAAAGGT[A/G]AAGTAACCTTCATAT | 9690 |
rs777675625 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175468 | GGAACGCAGCATAAG[C/T]CACTGCCGTGACTTT | 9690 |
rs777677064 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178753 | GAGAATGCTTGAAGT[A/G]TTTTCGTCTGAGAAT | 9690 |
rs777709717 | snp | A/G | 7.61412e-05 | 0.00616967 | intron-variant | UBE3C | GRCh38.p7 | 7:157189011 | TTCCGAGACAGATGC[A/G]TACATGAAAACCGGG | 9690 |
rs777726935 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202344 | CCTAGTACTCTGTTG[C/T]TGAATTTTTCCTCTG | 9690 |
rs777729960 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201658 | TTTTTTTTTTTTTTT[A/T]AAGAAATGTTTTGAA | 9690 |
rs777733207 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247721 | GCATAAGTAATATTT[C/G]TTGACATGTGAAAAT | 9690 |
rs777748449 | in-del | -/TTATC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181922 | ACGAAAACATGGTAG[-/TTATC]TTAATAGAGAAGACA | 9690 |
rs777748526 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158055 | CTCTTTTTTCCTTTT[-/TT]TTTTTTTTTTTTTTT | 9690 |
rs777749429 | snp | A/G | 1.65594e-05 | 0.0028774 | intron-variant | UBE3C | GRCh38.p7 | 7:157163896 | ATACTCTGTAGATAA[A/G]CATTTTTTCTACAGC | 9690 |
rs777750715 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157257024 | ACAAGCTGCTCTCGA[C/G]CCCCTCTCTTGGGGT | 9690 |
rs777768209 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147450 | TTGGAATTTCCTGCA[C/T]AGATAATCATTTCAT | 9690 |
rs777821077 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248246 | GCTTCCATCTTCGGT[A/T]CTATGAGGAGAAAAT | 9690 |
rs777823319 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238764 | TGGAGAAGAGAAGAG[A/T]TGAAGAACTGAGCCC | 9690 |
rs777839390 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150440 | GAACAAATTTCTACA[G/T]TTAGAAACGTAAAAA | 9690 |
rs777851641 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264358 | TGCTCGGCCTGTTAC[-/AC]ACACACACACCTGGT | 9690 |
rs777884992 | snp | A/T | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139938 | CCAAGACGAGGGCAA[A/T]TATTTGCCACCAGCC | 9690 |
rs777917392 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239490 | CTAGGCATTTTCTGC[A/G]CTGTGGACTAAGTGC | 9690 |
rs777941523 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244194 | GAGATCGTGCCATTC[A/T]TTGCGCTCCAGCCTG | 9690 |
rs777942465 | snp | C/T | 1.68459e-05 | 0.00290219 | intron-variant | UBE3C | GRCh38.p7 | 7:157223355 | GAACGAGTAAAGGTA[C/T]GCAATTTGGCTTCTT | 9690 |
rs777949190 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241110 | CCTCCCTTCTGTGCC[C/T]GGTGGTTCAAGGGTG | 9690 |
rs777956614 | snp | A/T | 1.697e-05 | 0.00291285 | intron-variant | UBE3C | GRCh38.p7 | 7:157175076 | GTATATAATGTATTG[A/T]TCACCTTGTCTAGGG | 9690 |
rs777959790 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143815 | GGGGTTATCAACAGA[A/T]TGGTGGCTTCGAACA | 9690 |
rs778016396 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157217393 | CCAGCCTGAAGTGAT[A/C]TTCCTACCTTGGCCT | 9690 |
rs778022028 | in-del | -/ATC | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137982 | CAATGTCTCTATGAA[-/ATC]ATCATGTTGCACACC | 9690 |
rs778022445 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168689 | GCTAAGTGAAGAAAA[C/G]CAGACACAGCATATT | 9690 |
rs778029041 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232777 | CATTGGTGGTTCTGT[C/T]TTCCGAGAAGCATAG | 9690 |
rs778042201 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160233 | GTGCGCGCCACCACG[C/T]CCAGCTGATTTTTGT | 9690 |
rs778045514 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182305 | TTTTCTATTTCGTTT[C/T]AACTGTTGGCGAAAA | 9690 |
rs778052560 | snp | A/G | 1.65949e-05 | 0.00288048 | intron-variant | UBE3C | GRCh38.p7 | 7:157184068 | GGGGGCTGCGATGCA[A/G]GCAGCCCCGTCGGAT | 9690 |
rs778065398 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175203 | TTTTACTGTAGGTGA[-/T]TTCAGGCCGGCATGA | 9690 |
rs778086561 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198062 | CTCCAGGGGGATCTC[C/T]CCTCTTTTAACAAAC | 9690 |
rs778128485 | snp | A/C/G | 3.59649e-05 | 0.00424045 | intron-variant | UBE3C | GRCh38.p7 | 7:157170278 | ATACTATATTTATGG[A/C/G]TCATTTTGTTTTGTT | 9690 |
rs778129384 | snp | A/G | 0.000115318 | 0.00759249 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182233 | ACGAGCCCTTTCTGA[A/G]TGCACTGTTGTTAAT | 9690 |
rs778175823 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157167970 | CTCAAGTCAATGAAA[A/G]TTGGAATTTTCTCTT | 9690 |
rs778195371 | snp | C/T | 1.65419e-05 | 0.00287588 | intron-variant | UBE3C | GRCh38.p7 | 7:157225382 | TTTTGTTTCTAATAA[C/T]CTTACAGCTTTCCTT | 9690 |
rs778211257 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198517 | CCTCCGCCATCTTCC[A/G]CTGGCTGTATTTGTC | 9690 |
rs778219376 | snp | C/T | 1.65883e-05 | 0.00287991 | intron-variant | UBE3C | GRCh38.p7 | 7:157207375 | AAAGTGACTGGTTTT[C/T]TTCTTCTTTTCTTTA | 9690 |
rs778272090 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172314 | GCTGGGATTACAGAC[A/G]TGAACCACCACACCC | 9690 |
rs778291186 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227677 | TGCACTCCAGCCTGG[C/T]AACAGAGTGAGACTT | 9690 |
rs778296570 | in-del | -/GT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184665 | ATTGATTACTACTAA[-/GT]GTAATCACAGAATAT | 9690 |
rs778330047 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152420 | GAAGCCAGGGAAATC[A/C]AGGGAGAAGCACCCA | 9690 |
rs778342841 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260908 | CGAGAGCCTTCTCCA[C/T]CTCCGTGATGCCTCC | 9690 |
rs778378620 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175341 | AGGCCAGCCAAAAGA[A/G]GACTCCTGATGTGTG | 9690 |
rs778413766 | snp | A/G | 6.6379e-05 | 0.00576065 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170359 | TGTCACAGTCCGGGG[A/G]CGCTTTTCCCATTGC | 9690 |
rs778441502 | snp | A/C/T | 0.000154981 | 0.00880174 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139240 | CGGCTGCTTCCGCGG[A/C/T]GGCGCTGCCCGCACA | 9690 |
rs778510111 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224714 | TCTATTTGCATGGTG[-/A]ACAAAAGAGTTTCTT | 9690 |
rs778533857 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265384 | TAATGGTGTTTGTGT[A/G]TACGAGGAAGGTGGA | 9690 |
rs778535155 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174571 | GATCCTCCCATCTCA[G/T]CCTCTCGAATAGCTG | 9690 |
rs778570977 | in-del | -/A | 1.70148e-05 | 0.00291669 | intron-variant | UBE3C | GRCh38.p7 | 7:157216857 | CGCGGATATGTTCTT[-/A]TCTTTTCAGGTTATC | 9690 |
rs778574403 | snp | A/G | 1.69269e-05 | 0.00290915 | intron-variant | UBE3C | GRCh38.p7 | 7:157220795 | AGTTCTCTAGGACAC[A/G]GGGTTACTGAGGTAT | 9690 |
rs778578005 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157228656 | TCCCAAGGGTGACAC[A/G]GACACTGACCCAGAG | 9690 |
rs778586529 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250009 | AATATTCCAAAATTT[-/G]GGGGGAAAAAATACA | 9690 |
rs778594276 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265941 | ATTATTTAAATTCTG[A/G]CACAAGCAAGCCACT | 9690 |
rs778615958 | in-del | -/TTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158051 | TACACTCTTTTTTCC[-/TTTTTT]TTTTTTTTTTTTTTT | 9690 |
rs778622388 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181604 | CGAGTTCCTATAGCA[A/G]AAATTTTGCTAGAGA | 9690 |
rs778636183 | snp | C/T | 1.65452e-05 | 0.00287616 | intron-variant | UBE3C | GRCh38.p7 | 7:157163885 | ACAGTTTTGTAATAC[C/T]CTGTAGATAAGCATT | 9690 |
rs778644381 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183715 | TTCTGACATGAACGG[A/G]GACAAAATCTAAATA | 9690 |
rs778653859 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153326 | AAACCCCTTTACTGC[A/C]AAAGACGAAATTTTA | 9690 |
rs778667627 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223551 | CTGAAAGTATTTTCT[C/T]AGTTACAACTGATTG | 9690 |
rs778691855 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146476 | TCTGCCCGCCTGGGC[A/G]TCCCAAAGTGCTGGG | 9690 |
rs778698885 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155965 | ATCCTTACGGGTTCT[A/G]CATCTGCATAATTTG | 9690 |
rs778699021 | snp | C/T | 4.95896e-05 | 0.00497919 | intron-variant | UBE3C | GRCh38.p7 | 7:157220683 | AACCAGGATTGCCCC[C/T]GACAGGTCACTCAGC | 9690 |
rs778706762 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268816 | GCACTTTATCAGGAC[C/T]TGACCTGTTGCTGGG | 9690 |
rs778717792 | snp | A/C | | | | | GRCh38.p7 | 7:157190978 | TTCTCAGGGGCTTGG[A/C]TCTTTTACCCCATTG | 9690 |
rs778732359 | in-del | -/GTT | 0.000233092 | 0.0107931 | | | GRCh38.p7 | 7:157248345 | ATATTCGATGCTAAC[-/GTT]GTCACTGTTCTCTTT | 9690 |
rs778759655 | snp | A/G | | | | | GRCh38.p7 | 7:157213060 | ACCACGCCCGGCAGT[A/G]TGTGCATTTCTGAAT | 9690 |
rs778796422 | in-del | -/CTGT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175645 | TTAATTTTCTGGACA[-/CTGT]CTGTAATATTTGTTT | 9690 |
rs778822495 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174190 | CAACATGGCAAACCC[C/G]GCCCCTACTAAAAAT | 9690 |
rs778864179 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212044 | TTTTATATATTCTTC[C/T]TATGAAGTCAAATTG | 9690 |
rs778888241 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236022 | TTTAATGCATATGTT[-/A]AGTGATTGTTTACTG | 9690 |
rs778900136 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259992 | GTTTGTTTCAAATAG[A/G]TCAATCATCGACGCC | 9690 |
rs778901079 | snp | A/G | 3.29457e-05 | 0.00405854 | intron-variant | UBE3C | GRCh38.p7 | 7:157178888 | GTGGCTCAGCATCCT[A/G]ATGGGGAGTGAGCAG | 9690 |
rs778903815 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159861 | CCTGATCTAATTACA[C/G]ACATGTAAATCAGAA | 9690 |
rs778911547 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157255054 | GAGACGGAGGTCGTG[-/A]GATCTCAGTGAGCCG | 9690 |
rs778921990 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157359 | AACAAAGGGAATATT[G/T]GTAGCATCATGAAAA | 9690 |
rs778927608 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263861 | CCATTCTAACCATTA[-/T]TTTTTTATGTTTCCT | 9690 |
rs778959891 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216227 | TTTTTCCCCTAGTGC[C/T]GTTAGTACATTATTT | 9690 |
rs778968064 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239656 | AACTTGAGCAGCCGC[A/T]TAAGGGATATGGGGC | 9690 |
rs778984201 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138189 | GATGGGTTTATTGTA[A/G]CATTAAATACATTTT | 9690 |
rs778987715 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260840 | GCCAGACGTAGGTTC[C/T]AGACATTCTGACAGC | 9690 |
rs778990144 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248745 | TCCAAAGCACCTTAG[C/T]CCTGGCGTCTGAGCT | 9690 |
rs779017169 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206752 | CACCTATCACCACAC[C/G]TGGCTAATTAATTTA | 9690 |
rs779035775 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203315 | TGGCTAAAGCAGAGA[C/T]AAAAGACTCCTACAA | 9690 |
rs779049721 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204971 | CCTTGTTCTCAAGAT[C/T]TAGACAGAGGTTAGG | 9690 |
rs779057857 | snp | A/G | 1.6513e-05 | 0.00287336 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207714 | TTAGTTGTAGGTCAA[A/G]GACAATCATCAATGA | 9690 |
rs779111527 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157155286 | CTTTGAAGTGTATAA[A/G]ATGGCTAGCATTATG | 9690 |
rs779140298 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157181066 | CACAAATCAGAGACA[A/G]ATTATAAGATCACAA | 9690 |
rs779173365 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226161 | GCCATTTATATTCTG[C/T]GTTTTTGTATAAATA | 9690 |
rs779194521 | snp | A/C | 1.68255e-05 | 0.00290043 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207892 | GCTCTGAAATGCAAC[A/C]ATGCATACAGATGGA | 9690 |
rs779221455 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164295 | TCCTGTAGCTGGGAC[C/T]ACAGGTGCATGCCAC | 9690 |
rs779221517 | snp | C/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138600 | GTGCCTCGCACTCCA[C/T]CTTTCCCGCACCCTG | 9690 |
rs779231732 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208932 | GCTAGATTTACAGTC[C/T]GTTTAATACCAGCGA | 9690 |
rs779242914 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183897 | CCTCTCTGAGGAAGG[A/G]CTGCTGGTGTATTTG | 9690 |
rs779247325 | snp | C/T | 3.30967e-05 | 0.00406783 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231300 | TTTTGCCAGACATTA[C/T]TACTTCCTAGGCAGA | 9690 |
rs779257984 | snp | C/T | 1.65583e-05 | 0.00287731 | intron-variant | UBE3C | GRCh38.p7 | 7:157225369 | GTTGTAAGAGGTCTT[C/T]TGTTTCTAATAACCT | 9690 |
rs779266182 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220166 | CAGTGGGCTGAGGTC[A/G]CACCACTGCATTCCA | 9690 |
rs779272487 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161484 | TGAGACAGGGTCTCG[C/G]TTTGTGACTCCAGCA | 9690 |
rs779273961 | snp | A/G | 1.75993e-05 | 0.00296637 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157182111 | TTTCTTTTTCAGGCA[A/G]CAAGTTTTTACAGCC | 9690 |
rs779276507 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157201721 | CCTATTCCTTTTTAG[A/G]CTTCTCTACAGTTTA | 9690 |
rs779279563 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240207 | CTACGGACACCCACC[A/G]CCACGCCCGGCTAAT | 9690 |
rs779281742 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165951 | TCTTTTGATGCTTTT[A/C]GAATTCAGTCTTTAT | 9690 |
rs779356461 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209535 | AACTTATAATTCTTA[C/T]ATAAGCTTTTCCTGG | 9690 |
rs779369016 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145032 | ATGCCTGTAATCCCA[A/G]CACTTTAGGAGGCCG | 9690 |
rs779384679 | snp | A/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223296 | TGTCTGAGGAAAGAC[A/T]GCTTGCTGTCCTGAC | 9690 |
rs779411187 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183410 | GCTTCCATGCCTTCT[C/G]CAGGCACTCCACACT | 9690 |
rs779432775 | snp | A/G | 5.18488e-05 | 0.00509134 | intron-variant | UBE3C | GRCh38.p7 | 7:157216850 | GTGTGTGACGCGGAT[A/G]TGTTCTTTCTTTTCA | 9690 |
rs779474889 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142505 | AGTAGAATTGTTTGG[A/G]GCTTAGTCCTGAAGG | 9690 |
rs779477911 | snp | A/G | 1.80208e-05 | 0.00300168 | intron-variant | UBE3C | GRCh38.p7 | 7:157170270 | GTGTCCAAATACTAT[A/G]TTTATGGGTCATTTT | 9690 |
rs779501862 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157172139 | TGGGTTCAAGCGATT[C/G]TCCTACCTGAGCGCC | 9690 |
rs779528485 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197997 | TATTCTTGATCCTGA[C/T]GGTCCTCCATATCCC | 9690 |
rs779531494 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184218 | ACCGCTTTGTTAGCA[C/T]GTTCATGGAAGTGTA | 9690 |
rs779544581 | snp | C/T | 1.6888e-05 | 0.00290581 | intron-variant | UBE3C | GRCh38.p7 | 7:157175069 | CAGTAACGTATATAA[C/T]GTATTGATCACCTTG | 9690 |
rs779563083 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257887 | ATAATTAGATAAGTA[C/T]TGTATGTGATTTGTG | 9690 |
rs779563503 | snp | A/G | 8.31981e-05 | 0.0064492 | intron-variant | UBE3C | GRCh38.p7 | 7:157220659 | GTGCTAGAGCACAGG[A/G]GAGTTCTGAACCAGG | 9690 |
rs779575540 | snp | A/G | 1.66214e-05 | 0.00288278 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157170355 | ACCTTGTCACAGTCC[A/G]GGGGCGCTTTTCCCA | 9690 |
rs779600624 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157244854 | TTCCATATACCTATT[-/G]GCTATTTTTTTCATG | 9690 |
rs779630181 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157235310 | AAAGGTGAGTGTTCT[A/G]CTAGACTAACCTGAA | 9690 |
rs779651670 | in-del | -/CTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158050 | GTACACTCTTTTTTC[-/CTTTTT]TTTTTTTTTTTTTTT | 9690 |
rs779663816 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157174069 | GACTAGCTACACTTA[A/C]GAGGCTATCTTTGCC | 9690 |
rs779710654 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248566 | GTGGTGAACAATGAC[C/T]TGGGAGAGGCGCAGG | 9690 |
rs779737123 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154753 | TACTTCATTTTTTCT[C/G]TAGTCAAGTGAAGCA | 9690 |
rs779754684 | in-del | -/TGA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206101 | CTGTTAACCTGTGAT[-/TGA]TTTGACTTGGTAGAG | 9690 |
rs779766515 | snp | C/T | 2.55751e-05 | 0.00357588 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186999 | CTGATGGTGCAGCAC[C/T]GCATGATGGTACCCA | 9690 |
rs779774310 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189568 | TGACTGCATTTGTGA[A/C]CCTACTTACATGTAG | 9690 |
rs779785744 | snp | C/T | 1.6784e-05 | 0.00289685 | utr-variant-5-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157139269 | CATGGGCTAGGCTGC[C/T]AGGATGTTCAGCTTC | 9690 |
rs779786424 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162635 | GCCTTGACCTCCTGG[G/T]CCTAAGTGATCCTCC | 9690 |
rs779797850 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192205 | CATTTGTGAATGATA[A/G]TTGTTTCCCGGGAAA | 9690 |
rs779805429 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232688 | AATTAGAAATTAATG[G/T]TGCTATTGTGATTAA | 9690 |
rs779838310 | in-del | -/TA | 2.15985e-05 | 0.00328615 | intron-variant | UBE3C | GRCh38.p7 | 7:157207944 | ATTTAAGGTATAGAG[-/TA]TATGTATTTTTTTGT | 9690 |
rs779854437 | snp | C/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256972 | AGTTGTGGAAGGGTT[C/G]ACTGATGAAGAAAAG | 9690 |
rs779862004 | snp | C/T | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139778 | CTTTCCATGCTCGCT[C/T]CCGCATGGCATCAGG | 9690 |
rs779864931 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233152 | TCATTTGTTATATCA[A/G]CTATAAATTTGTGAC | 9690 |
rs779877277 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178770 | TTTCGTCTGAGAATA[C/T]TTACTTGCCTGTTTT | 9690 |
rs779878172 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268174 | GTCTGAGGGCTGAGA[C/T]GCCATGGGGCCGCTG | 9690 |
rs779889003 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205848 | TTCCTTTTCTCAAAG[C/T]GGTTGATGATGGCAG | 9690 |
rs779900374 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263911 | TTTATCTACCTACAT[A/G]AGTGTGTGTTAATGT | 9690 |
rs779922654 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193731 | CTTTTTGATTACATG[A/C]ATCATGCAAAATGAC | 9690 |
rs779926431 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210709 | ATCAACCAAAGAACG[C/T]AGAAGCGTTTAGCCC | 9690 |
rs779935978 | in-del | -/A | 1.64901e-05 | 0.00287137 | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181616 | CAAAAATTTTGCTAG[-/A]AGAATGTTCTAAAAC | 9690 |
rs779936054 | snp | C/G | 3.30366e-05 | 0.00406413 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183880 | TTGTTTTGCAAAGGG[C/G]CCCTCTCTGAGGAAG | 9690 |
rs779953692 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266292 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 9690 |
rs779977728 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157183599 | TTCTGAGTCCCCTAG[A/G]TGGCCTCACCATAAG | 9690 |
rs779979820 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157209322 | GATTGCACTGAATAC[A/C]GTCCTAATGCATCGT | 9690 |
rs780064404 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157144047 | ACTGCGGAGCTGGGA[A/G]GAATTGGGTGATTTG | 9690 |
rs780090998 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221588 | TCTACTAAAAATACA[A/G]AAAACTAGCTGAGCG | 9690 |
rs780093456 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170980 | GTTAATGTTAAGGCT[A/G]ATTTTTTTTTTTGTA | 9690 |
rs780095399 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143626 | CTGGGTCATGTTTCC[-/T]ACCTGATAACCTCAG | 9690 |
rs780146908 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158800 | TTAGAAGAAATGCTT[C/T]AAAATCTATTGTTGA | 9690 |
rs780152913 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157259134 | AGCAGCTGCAGCATC[A/T]CTTGAGCACATGTTA | 9690 |
rs780162192 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157147598 | ATTATAGTTGAAAAG[A/G]AGTGGTGAGAACTTG | 9690 |
rs780184222 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223779 | ACAAAAGTTAGTTGG[G/T]CGTGGTGGCATGTAC | 9690 |
rs780215324 | in-del | -/AA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229931 | TTTATTTATTTTTTT[-/AA]TTTTTTTGAGACTGT | 9690 |
rs780231196 | snp | A/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223283 | CCGCCGCTGTCTGTG[A/T]CTGAGGAAAGACAGC | 9690 |
rs780252633 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196921 | TTGTGGTGAGCGGAG[A/G]TAGCGCCATTGCACT | 9690 |
rs780265396 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197191 | ACTACAGACAAATTT[G/T]CAACTTATTTGATCA | 9690 |
rs780305865 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant | UBE3C | GRCh38.p7 | 7:157207700 | CTGGATTGTGTTTTT[C/T]AGTTGTAGGTCAAAG | 9690 |
rs780315185 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157231184 | GAGTTTTTAAATGAA[C/T]TACTGAAGTCAGGAT | 9690 |
rs780366335 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168334 | AGCAAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 9690 |
rs780368185 | snp | A/G | 1.74127e-05 | 0.0029506 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267769 | GAAGCTGATGCTGGG[A/G]TCAGACCCCTACAGA | 9690 |
rs780372466 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142755 | ACTGTGCTCACTCCC[C/T]GGGTAATGGGATCAT | 9690 |
rs780393275 | snp | C/G | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178702 | CAGGTTGCTGCAAAA[C/G]TGTAATGATGACAGT | 9690 |
rs780393837 | snp | C/T | 6.59914e-05 | 0.00574381 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207539 | TGATAACGAATTCTT[C/T]GGTGATCCCATAGAA | 9690 |
rs780410813 | snp | A/C | 7.21007e-05 | 0.00600376 | intron-variant | UBE3C | GRCh38.p7 | 7:157188980 | TGGAGACCTTTGTAC[A/C]CTGACATGGAAAGAT | 9690 |
rs780434270 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226468 | GTCAATGCCGAGGGG[A/T]TTAAAATGAAAGTTT | 9690 |
rs780448302 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179877 | TAGTTTGTTGAAAAC[G/T]TAGGGAAACAGTATT | 9690 |
rs780471218 | snp | A/G | 1.74011e-05 | 0.00294962 | intron-variant | UBE3C | GRCh38.p7 | 7:157225587 | AGGTGGAGGCTAGGG[A/G]ATTGTTTTAGAAAAT | 9690 |
rs780509161 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157174947 | AGAACTTAATTAAAC[A/G]CAGCTCTCTGTTTGT | 9690 |
rs780510227 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157152129 | GTGTTCAGCTACAGG[G/T]TGTGGCCAGAATGGG | 9690 |
rs780542243 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254429 | TCAGACTGAGTTTCA[C/T]TCTTGTCGCCCAGGC | 9690 |
rs780556032 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157164760 | GCTCTGCTTGCTGGG[G/T]ATACAGATAGTGAAT | 9690 |
rs780562059 | in-del | -/GTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216277 | CTCTTTCAGGAAAAA[-/GTT]GTACAAAATTGCACC | 9690 |
rs780566385 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219012 | AGGCAAAACAGATAG[A/T]GTGTGATCTTTTGCA | 9690 |
rs780576435 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268285 | GGTTAGGTTTGGAAA[-/AG]AGATGATGATGGTAA | 9690 |
rs780577219 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157254000 | TCCCTGTCACCAGCG[C/T]CAACCGGATTGCGTA | 9690 |
rs780585519 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157252107 | CTCCACTGCACTCCA[G/T]TGTGGGTGACAGAGT | 9690 |
rs780656414 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208770 | CAGGAAACCACCACC[A/G]GTGAGAATGTAACTG | 9690 |
rs780671614 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242289 | ATAGTGATTAGAGCA[G/T]GAGCTGTTGTTAGGG | 9690 |
rs780688076 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157141636 | GGGACCACGGTGTAT[A/G]TGTGGTCTGTTGTCG | 9690 |
rs780696191 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157183967 | CCTGCCAGCGCGAGC[C/T]GTCACGACTCAGCCA | 9690 |
rs780706849 | snp | C/T | 1.6537e-05 | 0.00287545 | intron-variant | UBE3C | GRCh38.p7 | 7:157201705 | TGTTCTGTGTTTTTC[C/T]CCTATTCCTTTTTAG | 9690 |
rs780748832 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143873 | GGACAGGGTGGGACT[C/T]GTGAGGTACTGCAAC | 9690 |
rs780756114 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211862 | GTAGTGAAGGAGACA[C/T]GCATTCAGCTAATGA | 9690 |
rs780783188 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157205140 | ATATTTGAGTCAGTG[-/T]TTATAGCAGAAAGAA | 9690 |
rs780792981 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210987 | TCAAATTTATAAACT[A/C]CTCTTGAAGTGTAAT | 9690 |
rs780793536 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157238152 | TATGAAATAAAAGCC[-/A]AATGAAGGTATATGG | 9690 |
rs780899989 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186869 | ATCATACATAACAGA[A/G]GAATGCCTGAAGAAG | 9690 |
rs780930914 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173551 | TTTCTTCCTCACCTC[C/G]TTTTTAAAAAATTTT | 9690 |
rs780951126 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203674 | TATTAAATTATTAAT[A/G]CTATTTTATGATAGG | 9690 |
rs780956720 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157198818 | GGATTACAGGCGTGA[A/G]CACCTGGCCCAGAAA | 9690 |
rs780964646 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240212 | GACACCCACCACCAC[A/G]CCCGGCTAATTTTTG | 9690 |
rs780966404 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240627 | TGAATTGGTTGCAAG[C/T]TCAGAGTGGTTACAA | 9690 |
rs780977636 | snp | A/G | 0.00015949 | 0.00892857 | intron-variant | UBE3C | GRCh38.p7 | 7:157217051 | AGAGAAGAATTAAGC[A/G]CTTTAAAATTATTTA | 9690 |
rs780983940 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171967 | CTGCCTCGGCCACCC[A/G]TAGTGCTGGGATTAC | 9690 |
rs780988412 | snp | C/T | 8.24722e-05 | 0.006421 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181635 | ATGTTCTAAAACCAT[C/T]GCACTTTACTTACAA | 9690 |
rs781007647 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148297 | TAGTAGAGATGGGGT[C/T]TCGCCATGTTGTCCA | 9690 |
rs781021682 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166612 | AGGCATGCTGGCGCA[C/T]GCCTGTAATCCCAGC | 9690 |
rs781045216 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157191929 | ATCAGTGATATTTTC[A/C]TTATAATCAATAGAA | 9690 |
rs781074910 | snp | C/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207494 | TTATCTTTTTAGCTC[C/G]TTGTTTAGTCATTCA | 9690 |
rs781075467 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157239560 | CCACAGGCTTGTGAT[G/T]AGGGCACTCTGCAGC | 9690 |
rs781077297 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265525 | AACTGTGAAAACCAG[A/G]TACGTATTCATTGCA | 9690 |
rs781081337 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165753 | TGTTATTTCAGTTCT[A/G]GAATTTTCTTTCATT | 9690 |
rs781083206 | snp | G/T | 7.02124e-05 | 0.00592463 | intron-variant | UBE3C | GRCh38.p7 | 7:157139368 | GGCGGGGCGCCCTCG[G/T]CTCGGGGCCTGCGCG | 9690 |
rs781107996 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242754 | ATAGAACTAGAAGTC[A/G]AGGAAAAAAAGGAAG | 9690 |
rs781170405 | in-del | -/TGCCCAGGCTGGTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266946 | GAGGTCTCGTTATGT[-/TGCCCAGGCTGGTC]TCGAACTCCTAAGCT | 9690 |
rs781206027 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208290 | TGTGTTACCCAGGCT[G/T]GTCTCAAATTCCTGG | 9690 |
rs781237354 | snp | C/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157248371 | TCTCTTTTGAAGGCT[C/G]TCTATGAGAACATGC | 9690 |
rs781239900 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179809 | ACTACAGAAATTAAA[C/T]GCATACTCATTTCAG | 9690 |
rs781248963 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254469 | GTGGCGCGATCCCAG[C/T]TCACTGAAACCTTTG | 9690 |
rs781255355 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258214 | AGCCTCCCAAGGTGC[C/T]GGGATGACAGGTGTG | 9690 |
rs781273961 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157241312 | GTTTATGCTTCAAAA[A/G]ACACCATCAAGAAAC | 9690 |
rs781309192 | in-del | -/TTTTCTGTGAGGTCACAAAGCCT | 1.65666e-05 | 0.00287802 | splice-donor-variant | UBE3C | GRCh38.p7 | 7:157178848 | CATGATTCACAATGG[-/TTTTCTGTGAGGTCACAAAGCCT]TAAGTAGTAGGCAGG | 9690 |
rs781347948 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220358 | GTGAATTTTTGATAA[C/T]AATAACTTAATTTTT | 9690 |
rs781360323 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251992 | TACAAAAAACTGAGC[A/C]GGGCGTGGTGATGTG | 9690 |
rs781373606 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233783 | ATACAGTACTCCACG[C/T]CAAAGTGTCTGCAAC | 9690 |
rs781388957 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157166633 | TAATCCCAGCTCCTC[A/G]GGAGCCTGAGGCAGG | 9690 |
rs781409275 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207224 | TTGTATTAATCTATG[C/T]TGTTTATTAACCTGC | 9690 |
rs781441956 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157165193 | AAATTCTCGGCCATT[A/T]TCTCTTCCATTAGTG | 9690 |
rs781497557 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208594 | TTTATTTTTCACTAA[A/C]TATTTCTTAGATTTT | 9690 |
rs781506750 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188418 | ATCGGAGGAAGTAGA[C/T]GTCAGTGAAACTGTG | 9690 |
rs781547989 | snp | A/T | 1.66059e-05 | 0.00288144 | intron-variant | UBE3C | GRCh38.p7 | 7:157182331 | GAAAATTATTTGGGT[A/T]TGAAATACAAGATCT | 9690 |
rs781550302 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267632 | AGGCTCCGACCTTGA[A/G]CGGCTCCCCACAGCC | 9690 |
rs781605915 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | UBE3C | GRCh38.p7 | 7:157257084 | TTTAAAGACCACTTC[A/G]TAATAAGAAAGGCAG | 9690 |
rs781628261 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189446 | CTACTGCAGTATCAG[A/T]CAACTAAAATAAGAA | 9690 |
rs781642728 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161558 | CCCAGTTCAAGTGAT[C/T]TTTCTGCCTCAACCC | 9690 |
rs781644342 | snp | A/G | 1.67008e-05 | 0.00288965 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253977 | ACTAAAATTCGGTGG[A/G]AAAGACATCCCTGTC | 9690 |
rs781657429 | snp | A/C | 1.67214e-05 | 0.00289144 | intron-variant | UBE3C | GRCh38.p7 | 7:157183853 | TGTTTAACTAAAATA[A/C]GTTTTAACTGATTGT | 9690 |
rs781671267 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157218411 | CTGAGATCACGCCAC[C/T]GCACTCCAGCCTGGG | 9690 |
rs781690749 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227510 | GAGACCAGCCTGGCC[A/T]GCATGGTGCAACCCT | 9690 |
rs781708695 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157151901 | CACAGTAAAGTGGCC[A/G]TCATCTGAGAACTCT | 9690 |
rs781719860 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157250975 | TGCCGATAATACTGG[A/C]ATCTGTTAAAAGCAA | 9690 |
rs781720748 | snp | A/G | 1.67248e-05 | 0.00289173 | intron-variant | UBE3C | GRCh38.p7 | 7:157207677 | ATGGAAAAAGAAACA[A/G]TAGAAAACTGGATTG | 9690 |
rs781733067 | in-del | -/T | 1.65031e-05 | 0.00287251 | intron-variant | UBE3C | GRCh38.p7 | 7:157256903 | TAAAGCATGTGTTCA[-/T]TTTGCCATAGGAGGC | 9690 |
rs781751458 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142814 | TATATTCTTGTAACA[A/G]ACGTGCATAGGTACC | 9690 |
rs781759454 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268826 | AGGACCTGACCTGTT[A/G]CTGGGTGATTTTAGT | 9690 |
rs781774826 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206250 | TCAATTTAATATATC[A/G]TAGCTCTTTTTTATT | 9690 |
rs796082492 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221657 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 9690 |
rs796094050 | multinucleotide-polymorphism | AA/GG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157210156 | ACTCCAGCCTGGGCG[AA/GG]AGGGTGACTCTCTCT | 9690 |
rs796097640 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233818 | TACAATCCCACCAAC[A/C]ATTTGTGAAGGTTTC | 9690 |
rs796099681 | in-del | -/GTT | | | cds-indel, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269174 | TCTTTTTTATTTTAG[-/GTT]GTTTTATGTTGAATG | 9690 |
rs796159500 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226770 | TGAATCCTTGCCATG[A/G]CCCTCTGATGCCGAG | 9690 |
rs796165383 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231924 | CACTCTTTGGGGGGG[-/G]AGGGAGGCTTAGAAA | 9690 |
rs796218428 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157212516 | GATTTTCTTATGATC[A/G]TCATTGCCATGAACT | 9690 |
rs796227268 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168351 | AAAAAAAAAAAAAAA[-/A]GGTCCTACTATGCTG | 9690 |
rs796230254 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224013 | TTATCAGAAACGATG[-/T]TTTTTTTTTTTCTGA | 9690 |
rs796238578 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221758 | AAAAAAAATTTGGCC[A/G]TTGTAAAAGGTGGGA | 9690 |
rs796259083 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224798 | CACACACACACTCTC[G/T]CTCTCTCTCTCTCTC | 9690 |
rs796282369 | in-del | -/AAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177945 | TTTTTTTTTTTTTTT[-/AAG]AAAAAGGAAAAACAG | 9690 |
rs796288250 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157199493 | TTATTTTTTTGAGTC[-/T]TGAGTCTTGTTCTGT | 9690 |
rs796288264 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161469 | CTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCGC | 9690 |
rs796360380 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204419 | AAAAAAAAAAAAAAA[A/T]TTCAGCTTCTCTGTT | 9690 |
rs796380477 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249286 | CACTCTGTCTCTGCA[C/T]GGGCCTGCTGTGGAC | 9690 |
rs796380747 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150482 | GAACTAATATGCATA[-/AG]AGAAGATGCATGGGA | 9690 |
rs796396294 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206788 | TCATAGCTCTTGATG[C/G]GTGAAAGGCTGCTGA | 9690 |
rs796415942 | multinucleotide-polymorphism | AT/TC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221478 | AGGCGTGGTGGCTCT[AT/TC]CCTGTAATCCCCAGC | 9690 |
rs796424532 | multinucleotide-polymorphism | CAC/TAT | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137091 | CAGGCGCCTGCCACT[CAC/TAT]CCTGGCTAATTTTTT | 9690 |
rs796449582 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177422 | CATCCTATGTTGTCT[C/T]TCACACGAGGCACCG | 9690 |
rs796450461 | multinucleotide-polymorphism | GAG/TAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157985 | TAGATATATATATAT[GAG/TAT]GAGAGAGAGAGAGAG | 9690 |
rs796455429 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157146415 | CTAGTACAGACGGGG[-/G]TTTCACCATGTTGGT | 9690 |
rs796473608 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230464 | CACTTTGGGAAGCCA[A/G]GGCGGGCAGATCACA | 9690 |
rs796507786 | in-del | -/CTCCCA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224808 | TCTCTCTCTCTCTCT[-/CTCCCA]CTCTCCCACTCACTC | 9690 |
rs796521817 | in-del | -/TCTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157265907 | AAATTTCCCTGATCA[-/TCTT]TCTTTTTTGTTAACA | 9690 |
rs796529104 | in-del | -/TG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187559 | CTAATTTTTTGTTTT[-/TG]TGTGTGTGTGTGTGT | 9690 |
rs796541505 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193349 | GACAGATCATTGGGT[A/G]TCTCGCTGTTTCTTT | 9690 |
rs796554494 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193994 | CATCTATAGGCACTG[A/T]ACTGATATGAACAAA | 9690 |
rs796588900 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148490 | AGTTTTGTAAAACTG[C/T]CCTCTATTATATAAT | 9690 |
rs796607034 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157194558 | GAAGAATTCTGAGGC[-/T]GCATGCCAGAAAGAA | 9690 |
rs796614311 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230584 | CCTGTAGTCTTAGCT[A/G]CTTGGGAGGCTGAGG | 9690 |
rs796648831 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157240196 | AGTAACTGGGACTAC[C/G]GACACCCACCACCAC | 9690 |
rs796697205 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186542 | AGTGCAGCTTGATGT[-/A]AAAAAAAAAAAGTAG | 9690 |
rs796717171 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237314 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 9690 |
rs796754568 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157162058 | TGGGTGACAGAGCAC[A/G]ACTCTGTCTCAATTT | 9690 |
rs796767185 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200313 | AATAAGAATGGAGTT[-/T]AGTTGTTGTTTATTT | 9690 |
rs796769924 | in-del | -/AAAAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153199 | TGGGACTCCCTCTCA[-/AAAAC]AAAACAAAACAAAAT | 9690 |
rs796804949 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224065 | CTGGGCTAGAAAGCA[C/G]TGCTGTGATCATAGC | 9690 |
rs796805352 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187591 | TGTTTTTTGTTTTTT[G/T]TTTTGAGATGGAGTC | 9690 |
rs796816158 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157139488 | GACTCGGGGCTTCCT[C/T]GCCGGATCTCGGGGC | 9690 |
rs796842307 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192639 | CCCAAGAAGAATAAG[C/T]GCAAGAGAAAGAAGG | 9690 |
rs796873521 | in-del | AC/TAT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157202022 | AGAGAGTATGGTTTT[AC/TAT]TGAAGGTAAGTTTCC | 9690 |
rs796875320 | in-del | CC/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189756 | GTGGGTTCTTTTTTC[CC/T]CCTCTTTCTCACTCT | 9690 |
rs796905052 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157993 | ATATATATATAGAGA[G/T]AGAGAGAGAGAGATA | 9690 |
rs796944399 | in-del | -/TC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180330 | ACTTTTTTAAAAAAG[-/TC]TCTGTGTATTTTTTA | 9690 |
rs796960305 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154887 | TGTAGGCTATACTGA[A/C]ATGTATTTAATAATT | 9690 |
rs796962252 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157143753 | TGAATGCCTGAGTTC[-/C]TGTGGGACAGGCACA | 9690 |
rs796971162 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168722 | ATGATTCCATTATAT[A/G]AAGTGTCCAGAATAA | 9690 |
rs796983866 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261307 | GCAAAACTCTGTCTG[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 9690 |
rs796987333 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242538 | TTTTTTTTTTTTTTT[A/T]AATTCCTACTGTCTT | 9690 |
rs796990999 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157197394 | GTCCTTCAACTAAAA[A/C]CTCAAACATACTTAT | 9690 |
rs796993286 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216353 | TTCCAGATTCGTGGG[-/T]TTTTTTTTTTTTAAT | 9690 |
rs796994533 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157249536 | CAGGCTGGTCTCGAA[C/T]TCCCGACCTCAGGTG | 9690 |
rs797011126 | snp | C/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138485 | CTTTCCCGCCTCACT[C/G]GAGTCTGGCACCAGA | 9690 |