SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147098500 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027989 | CATTGAATCTCTATA[A/T]GTTGTCTGTCCCTAT | 10477 |
rs147136458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019407 | TTAATCTTTTTTCTA[C/T]CTGTAATATAAACTT | 10477 |
rs147152683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017099 | TGGAGACAGAATTGG[G/T]CCAGGAATGCAACCT | 10477 |
rs147155812 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054693 | CTGCCTTGTTCTCTT[A/G]ACATTGTCTTGCAGA | 10477 |
rs147172868 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051462 | TACTGACCTACAAAC[A/C/G]TTTGTAATGAACTGA | 10477 |
rs147242072 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002718 | TTAAAATATACACCA[A/C]CTTTTAAGGACTTAA | 10477 |
rs147260709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037821 | AAAAAATTTAAAAAT[C/T]AGCGGGCATGGTGGC | 10477 |
rs147303156 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053950 | AGTCATACAGTATGT[A/G]GCCTTTTCATATTGG | 10477 |
rs147348574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985148 | AAGGTGATTTGATCC[A/T]GATTTATCCGATGAA | 10477 |
rs147359299 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051076 | GAGGCAATAACTATC[C/T]TGTATTTTTGGTCCA | 10477 |
rs147364765 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979113 | TCTTTTTTGAGGCAT[A/G]AGATATTCTATCTGT | 10477 |
rs147464227 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035028 | ATAAATGGCAAAATC[C/T]GCCTTGGAAAAGCTA | 10477 |
rs147578440 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013414 | ATGAGATTGGAAGAT[C/G]TATTTTCAAGGTGGC | 10477 |
rs147595281 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007191 | TTGGATAAATCAGAT[C/G]TTAATGCCCACTGCC | 10477 |
rs147682380 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994996 | TACTGTATTACTGCA[C/G]TAATTTTGTAGCCAC | 10477 |
rs147698894 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992692 | TTGGAGACAGAGTCT[C/T]ACTCTGTTACCCAGG | 10477 |
rs147744136 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029097 | ATTGAATAGTCCAGT[A/G]GCTAGAGTGCCATCT | 10477 |
rs147831811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014123 | ATGATGCCCATGTTT[A/C]TGACGTAAGTATTAA | 10477 |
rs147848082 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007859 | TAAGAAACTGAATTT[A/C/G]TAATTCAATTTTAAT | 10477 |
rs147900630 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032824 | TAAGCTGATAAGCAA[A/C]TTCAGCAAAGTCTCA | 10477 |
rs147909576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027333 | TTTGCTTTTCTGTAT[A/G]AGAGACTTGGTAGCT | 10477 |
rs147932789 | in-del | -/G | 0.0232847 | 0.105357 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063813 | TCAGATGGTAACTGT[-/G]ATGTGGTAGCTAGTC | 10477 |
rs147956167 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063541 | AGCACAAATAAACCC[A/G]TTCTTAAATTGAAAA | 10477 |
rs147969508 | in-del | -/AATA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039279 | TATTTCAAAATGGTG[-/AATA]AATTTTATAAATAAA | 10477 |
rs148008817 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036756 | TTAACTTTTCTTAAC[C/T]GTATGTATAGCTCAC | 10477 |
rs148096222 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009923 | TAAGCTAACTTTTCC[A/G]GTTTTTTAATACTTT | 10477 |
rs148160491 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053473 | AACCATTACTTACAG[A/G]AACATTGACCTCTTA | 10477 |
rs148205584 | in-del | -/T | 0.0618563 | 0.164627 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005540 | AAATTAGTATGTATC[-/T]TTTTTGGACTGATAG | 10477 |
rs148214722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059543 | ACCCAACATATTAAA[A/G]ATATTGTCATTTCAA | 10477 |
rs148220248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990686 | TTAATTATATCCCTG[C/T]GTGATCTAGCTTTAG | 10477 |
rs148220686 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000684 | CTCAGCCTCCTGAGT[A/G]GCTGGGACTACAGGC | 10477 |
rs148290757 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046156 | GAGTACCCCACATAA[G/T]TGCCAGCTATAGTAT | 10477 |
rs148359316 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978421 | TTCTCATTCTCTTTA[C/T]TTCTTTAATACAGCA | 10477 |
rs148373622 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992723 | CTAGAGTGAAATGGC[A/G]CAATGTCAGCTCACC | 10477 |
rs148379506 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044918 | ATAATACATTTTCTC[-/TT]TTCATATTATGTAGA | 10477 |
rs148442961 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017719 | AAAGGTTTTTTTGTT[G/T]TTCTTTGTTTGTTTC | 10477 |
rs148459179 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055480 | TTTGACTAACAGATG[A/G]TACATTTATGAGAAT | 10477 |
rs148483841 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997787 | CTGCATCTTTGTTTA[C/T]ATCTCTCGTTGCCTA | 10477 |
rs148511704 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061710 | AACTTCAGAAACTTG[A/G]GTAGCTGACTTGATA | 10477 |
rs148552835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043106 | GTTTTAAATAAAAGT[A/G]TATAACAGGTTGAGC | 10477 |
rs148599386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047253 | CTGTTAGAGGTCTGA[C/T]ATGTATTATTGGGAC | 10477 |
rs148643298 | in-del | -/TCT | 0.0248432 | 0.108648 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982581 | TTTTATGAGTCATAA[-/TCT]TCTTTAATGAAATTG | 10477 |
rs148689885 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994617 | TGAGTGAGGATACAA[A/G]TAAAGTCCAGTTGAC | 10477 |
rs148693353 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034779 | TTATTTCATTTCTAT[G/T]TATATTCAGGTTTCT | 10477 |
rs148739801 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027237 | TATTTATGTTTGTGC[A/G]TTTGTGCATAAGTTA | 10477 |
rs148862113 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004461 | AGCATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10477 |
rs148918620 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049287 | AAGACAATATACTTA[C/T]AGATGTTGATATTTA | 10477 |
rs148954830 | in-del | -/C | 0.276534 | 0.248588 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985952 | AACTCCGGAATGTTT[-/C]CTCAAGGTCACTGAG | 10477 |
rs148977873 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053319 | TATTATAGAAGAAAT[A/C]GTTTAAATAAATTTT | 10477 |
rs149003710 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995440 | AAGAATACAGTATGT[A/G]ATACATGTAACATAC | 10477 |
rs149019632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035846 | AAGGTCACATAATAG[G/T]TAATATAAGCTGATG | 10477 |
rs149066551 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041104 | AATAAAAAAATTAGA[C/T]GGGTGTGGCAGCACG | 10477 |
rs149116793 | in-del | -/CCTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025500 | TGTATACAGGTATAT[-/CCTG]TTGGGATATATGGCA | 10477 |
rs149127580 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015425 | TGAGACAAAGTAGGG[A/G]TAGATGATAGTACTT | 10477 |
rs149131251 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988899 | AGTCCTTTTATTTTC[A/C]ATTCTTCAAAAAAAA | 10477 |
rs149181571 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018731 | TCTTTGATTTCATAC[A/T]GTTGGTAACATCTTA | 10477 |
rs149195105 | snp | C/G | 0.279726 | 0.248226 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033229 | ATTGCCAAGACAATC[C/G]TAAGCCAAAAGAGCA | 10477 |
rs149249707 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993100 | CTCTGTTGACATTCT[A/G]TCAGTTTTATAAGGG | 10477 |
rs149303290 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997408 | TTTTGTTTTGTATGC[A/G]CATGTTCTCTTCAGT | 10477 |
rs149310176 | in-del | -/TGCC | 0.275732 | 0.248672 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025501 | GTATACAGGTATATT[-/TGCC]TGGGATATATGGCAT | 10477 |
rs149333097 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036883 | TGTTTATGTCAATTA[G/T]CCTGTGGTTAAATTG | 10477 |
rs149391174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984679 | CATTTTTAGTAATTT[G/T]GGTGGTTGGAATATG | 10477 |
rs149421314 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046833 | TAGATTTTATTCTGT[A/G]GTGCCTTTACAGCAC | 10477 |
rs149596008 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005728 | TTATATATTTTTTCT[A/G]TTTAACAGACCTACA | 10477 |
rs149668715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003882 | TGATATTTCTGCATT[C/T]TCTCAGGAAGATGTT | 10477 |
rs149685056 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044134 | GAGCATAACTGTCCC[C/T]CCACATTTTTCCCAA | 10477 |
rs149717548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987441 | TTTCCATATAGGAAG[A/G]AGCACAAATATACTG | 10477 |
rs149718643 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054891 | ATAAGGAATAGGAAT[A/G]GAGAGTGAGAACGAG | 10477 |
rs149735276 | in-del | -/TGTTGGCAAATGGCCCTAGTTTCTTGACT | 0.257732 | 0.24988 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013478 | CAGTTCCTCACTGGC[lengthTooLong]TGTTGGCCTACCTGT | 10477 |
rs149739627 | in-del | -/CAGTATACA | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009614 | TAACCAAATATATTT[-/CAGTATACA]CCAAAATAAACACTT | 10477 |
rs149748124 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021440 | CTCCCTTCCTTCCTT[C/T]CTCCCTCCCTCCCTC | 10477 |
rs149769521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991840 | GGATGGAGCAGGGCA[A/G]TGTGAGATTTCATCG | 10477 |
rs149773010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032722 | TAAATATGCCTCCTT[A/G]TTCCCAACTGATTCA | 10477 |
rs149827143 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035689 | ATTAGATTTTTTTTG[C/T]AATTTTTTTTAAGCT | 10477 |
rs149896522 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007174 | AACTATGGGATTACA[A/G]TTTGGATAAATCAGA | 10477 |
rs149914180 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979615 | AACAGGAAGTTTTTG[C/T]ATTCTGGCTACTTTG | 10477 |
rs149929896 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021182 | GACTACGAAACATGA[G/T]ATTAGTCAGGATTGT | 10477 |
rs149978088 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052274 | ACTTTGCAGGGGTGT[C/T]CAGGGGAAAGAATAC | 10477 |
rs150037135 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999240 | TGGCAGTTCCTAGTA[C/T]TCTGACGTTCCACAG | 10477 |
rs150045786 | in-del | -/ATA | 0.278664 | 0.248351 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026874 | TTGATTATTGATCAT[-/ATA]ATATTTTGTGTAATT | 10477 |
rs150082847 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992953 | AGAACTAATGTTCTC[A/G]GGGCAACCTACCACA | 10477 |
rs150136318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997192 | TTTAAGCTCATTTAA[G/T]TCTTTCATCTTTTTC | 10477 |
rs150152665 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036853 | ACCAGAAATATGACA[G/T]AGGAACTTAAATCTT | 10477 |
rs150160371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048717 | TTGCTTTCAACCTAA[A/G]TAAATATGATTCTTT | 10477 |
rs150209862 | snp | G/T | 0.00168535 | 0.0289799 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984026 | ATCCTTTTTGTCTCT[G/T]CTCATTTCACTAACA | 10477 |
rs150239843 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022760 | AAAAACCCCACAGGT[A/T]TACAGAAAGAGAGCT | 10477 |
rs150292850 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029315 | TGAGAATCAGCTTAT[C/T]AAATTCCTTGGAAAA | 10477 |
rs150360134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002001 | TAGTTTTCCAGCTGT[C/T]GCATATGGAGATTGA | 10477 |
rs150367376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014810 | CAAATGGGGATAATT[A/G]GGATATCCATCATCT | 10477 |
rs150416763 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046362 | ATTTCCATACCTGCC[C/T]TCGTATATCAAACTG | 10477 |
rs150450068 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989620 | ACTCTGTGTGACTGG[A/G]AACATTTTCCAAAAG | 10477 |
rs150524343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986113 | CAAAACTTTGGGCTT[C/T]CTGTGAACAGTAACA | 10477 |
rs150539782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024361 | CCTATTATCCACTCA[A/C]CTTGTACAAAAACAA | 10477 |
rs150593149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032517 | ATTTAGTATTTTTCA[A/G]TATCTTTATATCTTA | 10477 |
rs150679291 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003137 | GACAGGAAGTATAAT[A/G]TATGTGCCTTAATTA | 10477 |
rs150734252 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020759 | TTAAAGTGGGTTTCA[C/T]ATGTAATGCATAAGG | 10477 |
rs150750633 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060258 | CTGATGTAACTTTTA[C/T]GTTTTAAAAAAAAAT | 10477 |
rs150798195 | in-del | -/TC | 0.257454 | 0.249889 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041231 | CAGAGCAAGACTCCG[-/TC]TCAAAAAAAAAAAAA | 10477 |
rs150801956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994818 | TGTGGATACTAGTCT[C/G]TTTTATCATTTACTG | 10477 |
rs150835660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005128 | TTGGCTCACATAACT[G/T]ATAAAGTCAGAGTAG | 10477 |
rs150886045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038699 | TCTGTCTGATAAAAG[A/G]CTTGTATCCAGAACA | 10477 |
rs150893147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050298 | TGGGTTTTCTTCAAC[C/T]CTTTCAAAACTTGAA | 10477 |
rs150896973 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978727 | TCGTAGAATGAGGAT[C/T]AGAATACACTTCCCT | 10477 |
rs150939974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043830 | TCATGAATATTTCTC[C/G]ATGTCATTAAACAGT | 10477 |
rs151007216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017919 | ATCCCAGCTTCATGT[C/T]AGCCATCATCTTCCA | 10477 |
rs151061121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021968 | TTTTTCCCTTTTGGT[C/T]ACTTTTTTACTGTTA | 10477 |
rs151095014 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983582 | TTTAAACTTTTTTTT[-/T]GACAGATAAAATATT | 10477 |
rs151095444 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036809 | AGAAATATTTTGGTC[-/TTTA]TTTAGTAAATTTTGG | 10477 |
rs151122834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995558 | CTTTTTTTCTAATCT[A/G]TAAGGTTCTCAGTGT | 10477 |
rs151149881 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006795 | TGCAAATAGTAAATA[C/T]TAGTTAGAAACCCTT | 10477 |
rs151166230 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047433 | ACTTGTCTGTCTCTT[C/T]GACATACTTATCTTT | 10477 |
rs151263771 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989049 | ATCTACAGATAGTTT[C/G]TATTATTAGTTTTAT | 10477 |
rs151279154 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998689 | GCATGTCTATAGTTA[A/G]AGACTTAATGAGAAA | 10477 |
rs180791827 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979658 | AAAACCGCAGAGTCC[A/C]CCTGGAGACTGCAAA | 10477 |
rs180827523 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020149 | ATTGGGTGACTTTGA[A/G]CATAAATTTATTGTC | 10477 |
rs180851728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004237 | TTAGAGTTGAAACCA[A/G]TGGTGCAGTGTGTAG | 10477 |
rs180852207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059866 | CAGATTCAACTTTTG[C/T]GCTCACAGTACACTG | 10477 |
rs180857202 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989610 | AATACTCAGTACTCT[G/T]TGTGACTGGAAACAT | 10477 |
rs180865522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997823 | GCTTTCATCCTTCAA[A/G]TGGTAGTGATCTTTT | 10477 |
rs180868641 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033261 | AGCTGGAGGCATCAC[A/G]CTACCTGACTTCAAA | 10477 |
rs180873783 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011573 | AAAACTAAGTCAAAA[A/T]TTTTTTAAGAAAAAT | 10477 |
rs180873966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036270 | AGATCCACACATAAA[C/T]GGTCAGTTGATTTTC | 10477 |
rs180876122 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044135 | AGCATAACTGTCCCT[C/T]CACATTTTTCCCAAG | 10477 |
rs180879867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051702 | TGCATTTTAAGTATA[A/C]CAATTCTGAAGTATA | 10477 |
rs180881316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026363 | TAAACCCTAGGTAAC[A/T]CTTTCATTTCCATTC | 10477 |
rs181039254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985037 | ACAAGTTGTATTCAC[C/T]TGGGATGATCAGACC | 10477 |
rs181045420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001041 | TGTGATGAGATGGAG[A/G]ATATGACACACTGAC | 10477 |
rs181069554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029700 | CTGTTTCTTACTTTA[C/T]TGTCTAGGACAACCA | 10477 |
rs181091430 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016262 | TTTTAAATTTTTTAG[A/T]ACAGACAGGATCTCA | 10477 |
rs181091918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991998 | AGGGACTGCTCTGCT[A/C]CTTCTGTTACGTGAC | 10477 |
rs181097459 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056149 | TTGAAAGGGTTCCCC[A/G]TCAGCCAAATCTGCA | 10477 |
rs181097971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006568 | TTAAATATTAGGAAC[A/C]TGCTAAATATTTCTC | 10477 |
rs181100261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040199 | ATAAATGGAAGATTG[C/T]GTTATAGTCATATAT | 10477 |
rs181117112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023561 | CCAGTGTGAGGCATC[C/T]CTTACTTTCTTTAAC | 10477 |
rs181140462 | snp | A/G | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063808 | TATTGTCAGATGGTA[A/G]CTGTGATGTGGTAGC | 10477 |
rs181149359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047542 | ATATACATTATCTCA[A/G]TCATAGCAGTCTGAA | 10477 |
rs181164477 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034589 | GTAAATGACAAGTTA[A/G]TGGGTGCAGCACACC | 10477 |
rs181251229 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988860 | TTTAGTGTTTGCTAC[A/G]AGATTGTATCTCATT | 10477 |
rs181278486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031727 | CATTCCTTCTTTACA[C/T]CCATTTTTGGAGGCT | 10477 |
rs181298848 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003843 | GTGTGGTAGGTACTA[G/T]TCTAGGTAATTTACA | 10477 |
rs181306571 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019880 | TCTACTTTCTCAGCA[A/C]ATATCAAGTGTATGA | 10477 |
rs181311695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059518 | AACAATTTTAATACT[A/G]TATTAGTTAACCCAA | 10477 |
rs181316550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042950 | AAGCCTTTTCAATAC[A/C]GTTTACTGCTTCCTC | 10477 |
rs181438476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053175 | AGAGTGAATACCTGC[C/G]AACTACATGAACTTT | 10477 |
rs181530640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037079 | GTTCCAGAAGATTAT[A/G]ATAGAGCTGAAAAAT | 10477 |
rs181545238 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984220 | CTTTGCAAGTGCATT[A/G]AACAAAAATTGTAGA | 10477 |
rs181552350 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000648 | CAAGCTCTGTCTCCC[A/G]GGTTCACGCCATTCT | 10477 |
rs181656510 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991200 | AGAATTGTAGATAAG[A/C]AGTTATGGCCCTCTA | 10477 |
rs181688419 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015780 | CAGAAGCCTGGACTG[G/T]AGTATAATCACTAAA | 10477 |
rs181708333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039592 | CCTGAGCAACATGGC[A/G]AGACTCCCATCTCTA | 10477 |
rs181755142 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988522 | ATTTTTAGATGAGTA[A/G]TGATTATATTTTCCC | 10477 |
rs181760546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002806 | GTGTTCTTTCACTTA[C/T]CTTCGATTATCTTTT | 10477 |
rs181815184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051981 | CTGAAGACACTGGAT[A/G]CATTTCTGAGTCACT | 10477 |
rs181818805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036499 | TGTGTGGGCTTTCTC[C/T]GTGTATTCTGGTTCC | 10477 |
rs181823718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026442 | GTTTCTCTATCTTGT[C/T]TGTCTGAAGGTAGAG | 10477 |
rs181865400 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029355 | TGGTTTTAATTAGAA[A/T]TTTATTGAATTTGAG | 10477 |
rs181917271 | snp | A/C | 0.0437281 | 0.141251 | upstream-variant-2KB, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980409 | AGCCCGCCGGGTCCC[A/C]GCCGCGCTCTTTGTC | 10477 |
rs181933069 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012187 | CATGTTCCTTTCTTG[A/C/T]GTCAACACTTACTAC | 10477 |
rs181944157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031269 | CATTAAATCATGTTC[A/G]TTTATTATGTGGTTC | 10477 |
rs181963287 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055930 | AATGGTGTGTTAAGC[A/G]CAGTGCACCAAAATG | 10477 |
rs181998631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023696 | GGGTTGAGAGCATGG[A/G]CTCTATCTTGGTACC | 10477 |
rs181999975 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055538 | AGCCAACACTACCTG[G/T]ATTTTAGGACTGGAT | 10477 |
rs182002883 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038814 | TGAAGCTGTATGAAT[A/G]ACAGTGGTGCTTACA | 10477 |
rs182023105 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992552 | CTCTGTGTTGACTTA[C/T]ATCTGTGTATCTTGT | 10477 |
rs182031903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006952 | TTATAATACCTAACA[A/C]TCTAATATTTCTAGC | 10477 |
rs182035073 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034709 | AATTTCCTGGAACTA[C/G]CATGTCAGAATACCA | 10477 |
rs182176972 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981067 | AGCTTTGTTCGCGCC[A/G]GGCGCCCGCGTCGCC | 10477 |
rs182183353 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999227 | TGACCGCAAAGAATG[A/G]CAGTTCCTAGTACTC | 10477 |
rs182184469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000386 | AAAACTTTGCAAATA[A/G]GCATATATATTACTG | 10477 |
rs182201222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019246 | ATTACAGGTGTGAAC[C/T]GCCGCACCCGGCCTA | 10477 |
rs182205128 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037434 | TGGAACAGGATGTGG[C/T]GGTGGAAGACAGTAG | 10477 |
rs182205941 | snp | C/G | 0.0107781 | 0.0726147 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998461 | GGATAAGGAGAGTGG[C/G]GAAGGGGCAGGGGGA | 10477 |
rs182211756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027447 | AAATAGGAACTATTT[A/G]ACCCATTAAATAAAA | 10477 |
rs182227367 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012947 | AGTCAGGCCTTGTCC[A/G]CTCCCATATAGTCCT | 10477 |
rs182231662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029048 | TCCAATTTCATTTTT[C/T]TCCATATGGATAACT | 10477 |
rs182234987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053685 | CATTCCAATCGATAA[A/G]CCTACATTAACACAT | 10477 |
rs182253239 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047952 | CTTCCCTCATTAGGT[C/T]GTTTCATTGTACTTC | 10477 |
rs182441559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983477 | TATTAAATTTAAGTG[A/C]TGTACCTAAAATCAG | 10477 |
rs182460712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015470 | TAAAGACTAACAAAA[A/C]CAAAAAGACTACTTA | 10477 |
rs182579223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021195 | GAGATTAGTCAGGAT[G/T]GTGATGTTTTTGCTG | 10477 |
rs182588010 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058220 | AGAAATAAGGGTTTA[A/G]TAATGTGAATTTTGT | 10477 |
rs182599426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046064 | TTCTTCTGTTCATCA[C/T]TGTATTTTCAGTACC | 10477 |
rs182651818 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980846 | GGCCAGAGCCTCCTC[A/G]GCTTCTTTTTTTCCC | 10477 |
rs182784146 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005226 | TTGACTCCATGATTA[C/G]ACAGACTTTCTCCTT | 10477 |
rs182814129 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045515 | TTCTTTCTGCATATC[G/T]GCTCTCCCCGTCTCC | 10477 |
rs182820218 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033488 | CCATATGTAGAAAGC[C/T]GAAACTGGATCCCTT | 10477 |
rs182826401 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020939 | GAGGATAGGAAAGGG[A/G]AATTTTTATCCTTCC | 10477 |
rs182849505 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061513 | TGCTTTTAGGCAACT[A/G]CTTTAATAATAGAAG | 10477 |
rs182850416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035109 | TTATGGTTAGTATTC[A/C]TATTTTAAAATTAAT | 10477 |
rs182872048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009075 | ATTTGTATAAAATCG[G/T]TAAAAGGTAAAGAAG | 10477 |
rs182924488 | snp | A/G | 0.0845519 | 0.187422 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062175 | TCAGGAAGGAAGATA[A/G]TTTTTTTTTACTGGC | 10477 |
rs183042831 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048395 | AGTACTGTATTTTGT[A/G]TATTGTTAAAGCTTA | 10477 |
rs183048966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034870 | AAAAAAATTAGAATT[C/T]GAAAAATTTGAAGAA | 10477 |
rs183060094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986725 | ATCAGAATTCCATTA[C/T]AGTTTTGAATATGAT | 10477 |
rs183063705 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001276 | ATGAGGTAAAATATG[A/T]CACTTAATCAGGAAA | 10477 |
rs183070706 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017539 | GTGTATGTGTATTGT[C/T]TAAAGTCACCTCATG | 10477 |
rs183142312 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026796 | CACATGCTAATGGCA[A/G]TATTAGATCTATTGA | 10477 |
rs183142696 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999016 | CATGTGTCTTTTATT[C/G]TAGAGCATAAGAAAA | 10477 |
rs183150692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048723 | TCAACCTAAATAAAT[A/G]TGATTCTTTCTAAAA | 10477 |
rs183160042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994139 | AAAGACATTTTTCTC[A/G]TCTTCCCAGGTGCTT | 10477 |
rs183164104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024892 | ATGTAGCAATTTCAA[A/G]GGTAGAATTTCCCAT | 10477 |
rs183165987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054043 | ATTTCTTTTTAGCAC[C/T]GAATAATATTTCGTT | 10477 |
rs183173063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037666 | AAAGTTAAAAAAAAA[A/T]TTTAAGTTGACATAG | 10477 |
rs183272493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989896 | GGAAAATCAGCAAGT[C/T]TTGCATAGAGTGTAA | 10477 |
rs183280962 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004900 | TAAATCTTCAGACAG[A/G]CAATGTCTTACGAAG | 10477 |
rs183288060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020591 | TTCATAGTCATTTCA[A/G]TAATACCACTACGAC | 10477 |
rs183389248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993016 | ATGAGTTTTATGAAT[C/T]AAATATGTGCCTTGC | 10477 |
rs183392803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995909 | ACTTATTCTCATCTC[C/T]TATTTGGTTACCTGG | 10477 |
rs183421389 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035405 | TATTTTAAAATGTAT[C/T]TATAAAAAATATGAA | 10477 |
rs183421800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056785 | GAAGTGTCTGTCCAA[A/G]TATTGCTTATTGGTT | 10477 |
rs183426176 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025476 | TGATACTTCCTTTTC[C/T]TCTTTATTGTGTATA | 10477 |
rs183438506 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009562 | ATTATTTTATTTTAT[G/T]AATTATGGTTCTCTA | 10477 |
rs183451062 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049732 | TTTTTTACTTCATCA[A/G/T]TCTTTTTATATGTAC | 10477 |
rs183468107 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021427 | CCTCCCTCCCTTCCT[C/T]CCTTCCTTCCTTTCT | 10477 |
rs183475244 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041032 | AGGCGGGCGAATCAC[A/G]AGGTCAGGAGATCAA | 10477 |
rs183597530 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051837 | ATAGTGAATACATGA[A/G]CTAGTTTTATAATTA | 10477 |
rs183610871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036403 | TTCATTCAACATTGT[A/G]TTGTACTTACAACGT | 10477 |
rs183633236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007760 | CTACACTAGTGCTGG[A/G]CAGGAGAACTTTCCA | 10477 |
rs183699677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013647 | ACTGGGTTTCAAGAG[C/T]GAATATTCTGAAGCA | 10477 |
rs183704310 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057495 | CTTTTCTTGCATTTC[C/T]TCTGTAAGTTTGTAA | 10477 |
rs183718523 | snp | G/T | 1.68414e-05 | 0.0029018 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060653 | TTCTGTTTTTAATGT[G/T]ACTGTGCTTAGGTTA | 10477 |
rs183741428 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982029 | AAAGTTTTCCAAGAG[A/G]TAACTTCACCAAGAT | 10477 |
rs183752177 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033344 | GAGATATAGACCAAT[A/G]GAACAGAACAGAGCC | 10477 |
rs183779912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983333 | TTCTCAATTTGGTAT[A/G]GTGTTGATGCGGAAC | 10477 |
rs183782908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000236 | TTAAAGTAGCTTTCT[A/G]CAACATGGGGTTAAG | 10477 |
rs183790059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014670 | GGATAATCTTTATTG[A/G]TTGTTGTCTCTTGGA | 10477 |
rs183840443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055216 | GAAAGATGATTGAGA[C/T]GGAAACTCGAAGGGA | 10477 |
rs183852141 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038776 | TTAAAATGGACAAAA[G/T]ATTTGAATAGAGATG | 10477 |
rs183860302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028789 | GCCTTTTGTACATAT[A/G]TGTTGCAAAAATCTT | 10477 |
rs183905915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999767 | GCTTTACAATTGAGT[A/G]ACTGTAAAAGCTTGA | 10477 |
rs183936400 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028178 | ATTAATGTAATTATT[A/G]TAATGTAATTATACT | 10477 |
rs183939014 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044709 | TTGTTGTTTTGTATG[C/T]TTATAGATGGTAACA | 10477 |
rs183999240 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001144 | AAGTTTTGAACCACT[A/G]CTTCAGAAGAATGCT | 10477 |
rs184033001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030295 | TAAATTGAATATGTA[C/T]ATTTTTCTTTTGTAT | 10477 |
rs184035363 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001721 | TTTCGAAGGTGACAG[A/G]TTAGCATATAACCAG | 10477 |
rs184040853 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018711 | CAGTCCTCCAGGACT[A/C]TTCATCTTTGATTTC | 10477 |
rs184041686 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979175 | GAACCTAGCGAACTT[C/T]AATGAACTGTTCCCC | 10477 |
rs184081723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041477 | ATGGAGTCTCTCTCC[A/G]TCGCCCAGGCTAGAT | 10477 |
rs184100508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997441 | CATCTTCTTTCCTGA[C/T]GTACTTGAAATGTGT | 10477 |
rs184131731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058890 | GTGTTTAAAGTGCTT[C/T]ACCGTGTGGTCCCAT | 10477 |
rs184134093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023125 | TTCCTTGACTTACAG[C/T]GGGGCCGCGCCCCAA | 10477 |
rs184144575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034447 | AAACCAAACACCACA[G/T]GTTCTCACTCATAGG | 10477 |
rs184164312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016712 | ATCAGTCTCACGACT[A/G]TTATGATTTACTAGA | 10477 |
rs184177932 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063414 | AACACAATAAACATG[C/T]TCCTGAAGGCATAGT | 10477 |
rs184182806 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047471 | CTCATAAACTTCTTA[G/T]TCCCAGTGTATCCAA | 10477 |
rs184195134 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985284 | GCTATGCTGTCCGGT[A/C]ATGTAGCCACTTGCC | 10477 |
rs184219371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040878 | TTTTTTACCTTAGAA[A/G]AGCAGAAGACTTGAA | 10477 |
rs184281668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982900 | TGTCCTTGGGCCTCT[C/T]CACTCTGAAACTTGT | 10477 |
rs184333411 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000005 | TGGTTCTGGCCCACA[A/G]ATAGCAATGATCAGT | 10477 |
rs184352012 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988560 | AATAGAAGAATTTGT[G/T]ATTTTACTGTGAATG | 10477 |
rs184356117 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003446 | TCAAATTATTTATGT[C/T]TACTTTTGAAGAACT | 10477 |
rs184383804 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990805 | ATTGAATTACACACA[A/G]GTTAGAAATGTGTGC | 10477 |
rs184386409 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031481 | TTTTTGTTTTTTTGT[C/T]ATTTTAAAGTACCAC | 10477 |
rs184391105 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050730 | TAACCTTTCTGGCTC[A/G]GTTTCTCATCTGTGA | 10477 |
rs184398752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035667 | TCGAAAACTTCCTTG[A/G]AACATTATTAGATTT | 10477 |
rs184408707 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019319 | TGATAGACGCTAAAT[C/G]ATTGGAACATGTTCA | 10477 |
rs184520910 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005622 | TTAACTAATTTATAT[C/T]ACCTGTGTGGCACCT | 10477 |
rs184579890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990889 | TTTTACAAGTTCACA[A/G]TCCTTTATTTGAAAC | 10477 |
rs184599006 | snp | G/T | 0.000116462 | 0.00763003 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987332 | TACTTTCCATCTGTT[G/T]CCCAGAGGGTGTCCT | 10477 |
rs184619124 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034287 | CAACCCAAATGTCCA[C/T]CAATGATAGACTGGA | 10477 |
rs184634780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006032 | ATGGGCTAAGGACTG[A/G]GAGGCTGTCATAGTT | 10477 |
rs184644729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022840 | TTTTTCTCCACTCTG[C/T]GCATTGTCTGTAAAT | 10477 |
rs184686777 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010807 | CCTGTTGTCATATCC[C/T]CCTCTTTTTTTTTTT | 10477 |
rs184692610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035910 | CTCAGAATTTAAGAT[A/T]TATTTTGTTTGGTGT | 10477 |
rs184799147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026240 | ATATTCTCATAGAAA[C/T]AGAAAAACCAGTTGT | 10477 |
rs184820058 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051320 | TCCTTATTGGTAGAC[A/G]TAGTGGTTTTATGCA | 10477 |
rs184886319 | snp | A/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055695 | ATGTACACTTTGTCC[A/G/T]ATAGTTAAATGTACA | 10477 |
rs184926169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028540 | CAATAGTTCTCTTTG[C/T]GCTGCAGGTTTATCA | 10477 |
rs184930714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006319 | TACTTTCACTTGTTT[C/T]AAAGTAAAGGCACAC | 10477 |
rs184960377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054872 | ATATTTAAAGCTTAG[C/G]GTGATAAGGAATAGG | 10477 |
rs185077587 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038606 | ATAAAATAATTGGCA[A/G]GTGGAACTTAAAGTA | 10477 |
rs185083827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991395 | TCCCATTGGCATATC[C/G]AAACTGCCAGCATCA | 10477 |
rs185130742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001052 | GGAGAATATGACACA[C/T]TGACTCTTAAAGAGG | 10477 |
rs185136982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016646 | TTCTTTTTGCAAAGC[A/G]TTAGTGTTTCCCAAA | 10477 |
rs185137331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026388 | CCATTCCCTTAACAA[A/G]TAACTGCAGTCTCTC | 10477 |
rs185159067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029731 | AGTCATAATTGAGCT[G/T]CTTTTCTTGTTCCAT | 10477 |
rs185188998 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056404 | GTTCACCTGATGGGC[A/T]TCTGCATCTGTTGAG | 10477 |
rs185195060 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040235 | GAGCTTTCTGATATA[A/C]CCAGTTAAGCAATTT | 10477 |
rs185203112 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025806 | CATACCAAGTCTTCT[A/T]TAAGAACAATTCTAA | 10477 |
rs185217827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997252 | TTATCTATCTCTATT[A/T]ATTTTTTTTCTGTCC | 10477 |
rs185223823 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042616 | CAGGTTAGAATTCAG[G/T]TTCTGCCACGTATTA | 10477 |
rs185293911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010320 | TATTTCTTGTCAGTC[A/C]TATTCTGTATTTTCA | 10477 |
rs185322545 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978616 | ATCACGGAATCATGG[A/C]ATTTTTGAGCAGGAG | 10477 |
rs185373858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059348 | TCTGTTCACTAGTTA[C/T]AGCTGAAAATATATT | 10477 |
rs185375433 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980857 | CCTCGGCTTCTTTTT[G/T]TCCCTCCCCCCCCTT | 10477 |
rs185379416 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019990 | ACCTTTTGACCAATA[G/T]CTCCCCATTTCCCCA | 10477 |
rs185389719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999065 | ACTTGTTTTGAGGCA[A/G]ATGTAGTATGAATCC | 10477 |
rs185396080 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032627 | TTGATATTTATTTTC[A/T]TCTAAGAAAAATTTA | 10477 |
rs185430829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059789 | GTGTTGGTCCCCTAC[A/C]CCCTCCCTGTCATGC | 10477 |
rs185441058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043222 | TTTCATTGTATCCAT[A/G]GTATGTTCTATTTTT | 10477 |
rs185447400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012464 | GTGGCTAGGTGGGTG[C/T]ACACACACACATACA | 10477 |
rs185457100 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015523 | TAAATGATAAAAGTA[C/T]AATCTGGAGGAAATG | 10477 |
rs185493455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038942 | GGAAGGATGTGTAGC[C/T]GTTGAAACTCTCATA | 10477 |
rs185497717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062682 | AAATTTAGCTATTAT[A/G]TATGAAGATACTGCT | 10477 |
rs185627757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984283 | CTTTTTAGCATAAGT[A/G]TACATTGTGGATTTA | 10477 |
rs185628614 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029190 | TTGTCTATCTCTGCA[C/G]AAATAGTACATGATA | 10477 |
rs185630522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000451 | GGGGGTACCATTCAT[A/G]CTGTACTCTGTATTC | 10477 |
rs185636722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047191 | TCATGTAATTAATCT[C/G]TCCTCTGCTTTGTTT | 10477 |
rs185639188 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001030 | TTAAGATTTACTGTG[A/C]TGAGATGGAGAATAT | 10477 |
rs185698676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015982 | AATGAGAATGAGTCC[A/G]GAGTAATTAGCCATG | 10477 |
rs185741152 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030851 | TGTTATTTCTGTCTT[C/G]TCTCTGTCTTGTCAC | 10477 |
rs185749111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002296 | TCATGTTTAATCTAT[A/G]TTATTCATTAATGTT | 10477 |
rs185785656 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004238 | TAGAGTTGAAACCAA[C/T]GGTGCAGTGTGTAGT | 10477 |
rs185789142 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059879 | TGCGCTCACAGTACA[C/T]TGCTAGTTTTCAAAT | 10477 |
rs185803099 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033327 | GTACTGGTACCAAAA[C/T]GGAGATATAGACCAA | 10477 |
rs185838293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019093 | CTCAGTCTTCCAAGT[A/G]GCTGGGACTACAGGC | 10477 |
rs185865227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041800 | CCAGTGCTTTCACTA[C/G]GTGAATTGAATGACA | 10477 |
rs185867922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987842 | GCTGCTGACTGTCAG[C/T]ATCTGCGTCACAGAT | 10477 |
rs185922604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044254 | AAAGTATAATGTTCA[A/G]TAAGTACTGAAAAAG | 10477 |
rs185926639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020251 | GGAGCATCCTTCCTT[C/G]CCTCTATTAGCTTGT | 10477 |
rs185928356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048471 | AGTATGGATTAATAA[A/G]CAATACCATTTCCTG | 10477 |
rs185933296 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034971 | TTAGGAACTATTAGA[G/T]AAAGGGGAAAGACAA | 10477 |
rs186011082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023582 | TTTCTTTAACACAGC[C/T]GCCTGATAGAACAGT | 10477 |
rs186031583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992133 | TTTTTGGTTTGTTGG[G/T]TTTTTTGTCTTGTAA | 10477 |
rs186043646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047705 | ACCATATTAGTCTAG[C/T]CTATCATCATCTTTC | 10477 |
rs186170043 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006612 | TCAAATTTAACTGAG[C/T]AGTTTCTGTTTTTCT | 10477 |
rs186171946 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052656 | ACATTGGCTAGTCCT[A/T]TTTATTGTCTAGCAA | 10477 |
rs186174232 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985075 | TGAAGTCTGCTTGTG[A/T]TATAATAGGGTATAA | 10477 |
rs186201888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045024 | CTTCCTCTAGTAGTA[C/T]ACCTTGTGTTTATGC | 10477 |
rs186210528 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033358 | TGGAACAGAACAGAG[A/C]CTTCAGAAATAATAC | 10477 |
rs186305937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989052 | TACAGATAGTTTGTA[C/T]TATTAGTTTTATTGT | 10477 |
rs186309329 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037202 | TGCTGCCAGCAAATA[C/T]AATTATATGTAGTAC | 10477 |
rs186365458 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992661 | CCACCATGCCTGACT[A/G]ACTTTTTTTTTCTTT | 10477 |
rs186369933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007014 | ATAATTTAGCTTGAG[A/G]CATCTCTGAGCAGGT | 10477 |
rs186379333 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024013 | ATTTCTTTTGCATTT[C/G]TAACCTCTCCCAGTA | 10477 |
rs186404028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047958 | TCATTAGGTCGTTTC[A/G]TTGTACTTCCCATGT | 10477 |
rs186413820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034852 | AAATGATTTGAGTAA[C/T]AGAAAAAAATTAGAA | 10477 |
rs186419501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003941 | ATTCTTCAGAAATTA[C/T]ATAACTAGTCTAAAG | 10477 |
rs186465877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013162 | CAAATATGTTAATTG[A/C]AACAAAGGAAAAATA | 10477 |
rs186471419 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990855 | TTCATCATTATGACA[A/G]TACACAAGTTACTTC | 10477 |
rs186482209 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037632 | TGTTTTAAGCTCAGT[A/G]TTACTACAGAAGAAT | 10477 |
rs186492179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027615 | ATTTGAAGGTCCTTA[A/G]TAAAACAGTATGTAA | 10477 |
rs186495174 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026905 | TTTCTGTGGTTATTA[C/T]AAATATATGATTGAT | 10477 |
rs186512769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999273 | GGCTAAAGAAGAAAA[A/G]CTGAACATTTCAAGA | 10477 |
rs186541722 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053717 | ATTATCATGCAAAGT[C/G]CCTAGTTTTCATATG | 10477 |
rs186545294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029580 | CTTGTTTTTTATCTA[A/G]CAACCTTGTATAAAT | 10477 |
rs186552581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053314 | TTTAATATTATAGAA[G/T]AAATAGTTTAAATAA | 10477 |
rs186556697 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979682 | CTGCAAAAAGAATGG[C/T]AGAACAAACAAAACT | 10477 |
rs186560033 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997953 | CCTCTTGTCATGTAC[C/T]CTTTCATCCCAGCTG | 10477 |
rs186569097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011761 | AAATTGGATCATACC[A/G]TTATTTGTTGTTTTT | 10477 |
rs186586588 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007767 | AGTGCTGGACAGGAG[A/G]ACTTTCCACAATGGT | 10477 |
rs186586748 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056001 | TTTCTTACAACATTC[A/G]CACTGAAAGGAACCC | 10477 |
rs186713116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994817 | ATGTGGATACTAGTC[C/T]GTTTTATCATTTACT | 10477 |
rs186769025 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039694 | AAAATTCATCTCAAT[A/G]ATTTTATAATGACAA | 10477 |
rs186812199 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993078 | TGTAAAGCCTTGGGA[A/T]TTTTATCTCTGTTGA | 10477 |
rs186820391 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024571 | TTTTAATATATGTGA[C/T]TATTAAGATGTAATG | 10477 |
rs186856661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998720 | GCATCAAATTGTGGT[A/G]CAAACAGCTGAAAGT | 10477 |
rs186863094 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026695 | ATTTGTTCCGCCATT[A/G]CTTCAGGTAGATTTC | 10477 |
rs186920478 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041523 | GGCTCACTGCAACCT[C/G]TGCCTCCCAGGTCCA | 10477 |
rs186928228 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030658 | TCACTTGAAATTTGA[A/T]AGAAGTCTCCTGTAA | 10477 |
rs186938033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018832 | TCATGCCTTTTATAT[A/G]GGGGAGTGTTATTTT | 10477 |
rs186955703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058370 | TGAGTTTTGTTGGCT[C/T]TGAGTTCATTTGAAG | 10477 |
rs187042945 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980593 | CCCGCCCCTCCCCCC[A/C]GCGCTCGCCTCGGAA | 10477 |
rs187052520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036589 | TGAGTGAGTGAGGGG[A/G]TGTGGGGGTTATGTG | 10477 |
rs187063823 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012200 | TGCGTCAACACTTAC[C/T]ACATTAACAACACTG | 10477 |
rs187076154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061014 | TTCTCAATACCTTCA[C/T]TTAATTTGTTAATGG | 10477 |
rs187130380 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983570 | ATATTTGTAAATTTT[A/C]AACTTTTTTTTTGAC | 10477 |
rs187145148 | snp | C/G/T | 0.00756178 | 0.0610554 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033862 | CCATCAACAAGTGGG[C/G/T]GAAGGATATGAACAG | 10477 |
rs187190872 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061815 | ACTTCTAAATATTTG[A/G]TAAGTCACTAAAGAC | 10477 |
rs187194343 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028570 | AACTCTGACAATCTT[C/T]AGACTTCTTGATTTT | 10477 |
rs187352091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986839 | AAAGTTGAATGAAAC[A/G]CAAGAAAACTCAGCA | 10477 |
rs187366167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001533 | TTGATACAGCACCAG[A/G]TAAGTAGGTTTGCTT | 10477 |
rs187371386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017681 | ACGGAAGTGTCATAT[A/G]TTGCTTATTTAACAA | 10477 |
rs187402905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041173 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGGCTGC | 10477 |
rs187449029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005778 | GTATATGTATTTAAT[A/G]TTTTTGTGAATCTGA | 10477 |
rs187467549 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981225 | CGCCGGCCGTGGCTC[C/G]CCTCCGCGGGCGCGG | 10477 |
rs187484560 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034245 | ATGTTTATTGTGGCA[C/G]TATTCACAGTAGCAA | 10477 |
rs187511232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062254 | GTTTTTAAACATCAA[A/G]ATAAAAATTTATATC | 10477 |
rs187544274 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021733 | TGTGGTCATGGAACC[A/T]TATAAAGTAATTTAG | 10477 |
rs187556189 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990038 | TTTTTTTTCCACATA[C/T]CAATTTTGACAGGTA | 10477 |
rs187574929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004911 | ACAGACAATGTCTTA[C/T]GAAGAAAATATTTTG | 10477 |
rs187579699 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020832 | ACCTCATTATATCTG[G/T]ATTTCCCTGACATGG | 10477 |
rs187653402 | snp | C/T | 0.00910017 | 0.0668377 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989833 | TTAGTACTTTATGCT[C/T]TCCTTAAATGAGTTG | 10477 |
rs187693239 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025137 | AAATAATTTATAGGG[A/G]CACGAGTGGTTTGAA | 10477 |
rs187715169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002167 | CTGGCCTACTGATCA[C/T]ATCTGGAATGTTTTA | 10477 |
rs187722128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049241 | AAAAACAAGGGATTT[A/G]AGTGTGAAATTGTGA | 10477 |
rs187723222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010143 | CACATACTACTACTC[C/T]TACCATAATGGTGTA | 10477 |
rs187729710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046195 | GTAATTACATTGTCC[A/T]CCAAGGAAAAAGATC | 10477 |
rs187739387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035407 | TTTTAAAATGTATTT[A/G]TAAAAAATATGAATT | 10477 |
rs187747003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025571 | TAGTTGTAAAATACC[A/T]CATATTAATTTTTTT | 10477 |
rs187752530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996969 | TGAGCTTAATGTGTA[C/T]GTATGCACACATGGC | 10477 |
rs187753943 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021290 | TTACATTTTTCTGTC[C/T]TTATCCGAGTGTTAA | 10477 |
rs187777310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050200 | TTTCCTGAACAGTTA[C/T]TGAAGGTGTTTCAAG | 10477 |
rs187932712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021085 | AGTAATTATTTCAGG[A/G]AAAGGTGGTTTACAG | 10477 |
rs187962563 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990387 | TATAGATATTTGTTC[C/T]TGTACTTTGCCTCTT | 10477 |
rs187976125 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035120 | ATTCATATTTTAAAA[G/T]TAATGTACATTACAG | 10477 |
rs187993220 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009253 | CTAAGAGATTGGACA[C/T]ATTATAAAACAAATA | 10477 |
rs187994010 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038689 | TTTGAAAACCTCTGT[C/T]TGATAAAAGACTTGT | 10477 |
rs188001469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987541 | AAATAGTTTCTTGAT[A/G]TGGGAAAGGCCATAT | 10477 |
rs188145444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992141 | TTGTTGGGTTTTTTG[G/T]CTTGTAACTTGTATG | 10477 |
rs188151380 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006932 | CTTTAAAAGCCATGC[A/C]GAATTTATAATACCT | 10477 |
rs188166444 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055346 | TGATTCAAGACAGTG[A/G]AAGAGACAGAGAGTG | 10477 |
rs188174348 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038800 | AGAGATGTTACTGAT[C/G/T]AAGCTGTATGAATAA | 10477 |
rs188180677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028823 | TCTGTTAATGACTTG[C/G]TTCTTTTATGGTATA | 10477 |
rs188184675 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015209 | TTTAGTATAAAATTC[A/G]GGACATGCAAAAACA | 10477 |
rs188227372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057965 | AATTTTCGCATAATC[A/G]AGAATTTTAAAACAG | 10477 |
rs188255885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005256 | TGTGATCATAAGATA[A/G]CTGATAGTACCTCCC | 10477 |
rs188274313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055120 | GGAAATGCCTGTTGG[C/G]AATGAGTTCAAGTAA | 10477 |
rs188332482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059835 | ACACTTTTGAGAGCA[C/T]TTAATGTTTTCCTCC | 10477 |
rs188342301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043657 | ACAAGAAAGTAAAAT[A/G]TAATAATTAACGATA | 10477 |
rs188386722 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997641 | CTATCAAAAGTACCT[G/T]CATTTAGCTCTCTTA | 10477 |
rs188397236 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010984 | GCCAGCTTCAACTTC[A/G]CATCATACAACAGCC | 10477 |
rs188409194 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026355 | ATAATGAATAAACCC[G/T]AGGTAACTCTTTCAT | 10477 |
rs188481451 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028323 | GGTATATTGGGTGTT[C/T]CATGTTTATTTTGTT | 10477 |
rs188506116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999770 | TTACAATTGAGTAAC[C/T]GTAAAAGCTTGAGCA | 10477 |
rs188509965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054272 | GTAACAAGATTGCCA[A/G]ACTGTCTTCCAAAGT | 10477 |
rs188551186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050885 | AGAGCTCTGGTGTGC[C/T]TTGAAACTTCCTTCT | 10477 |
rs188579707 | snp | A/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063708 | AAAAAGAATATGAAA[A/T]CCTGGCTCGCTCACT | 10477 |
rs188587408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047512 | TTTTTCAACATCCAT[A/G]TCTTAGTTAATGGCA | 10477 |
rs188636072 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000119 | AACCCAATTTCTAGA[A/T]GTATTAGATACATAC | 10477 |
rs188674559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982942 | ACAAGTTAATACTCA[A/G]CAGCAGGAGAAACAT | 10477 |
rs188695350 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985995 | GGGAGTAGAATCTTT[A/C]AATGAGATAGGAGGT | 10477 |
rs188764319 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017198 | AAGGACATAGGGATC[A/G]GGAGTATGGAAGAAT | 10477 |
rs188764693 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040927 | TAGAGGTTCCTTCTG[A/G]TGCTTCAGCACATTT | 10477 |
rs188794768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003675 | GTTTGCACATAGTAC[A/T]CTGTGGAACCAGACT | 10477 |
rs188795131 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013963 | GCTGGAAGATCAGTA[A/T]CATGCTTCTAATAGT | 10477 |
rs188800548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019337 | TGGAACATGTTCAGC[C/T]GGTGCTCAAAATGTG | 10477 |
rs188805256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038095 | ACAGATACATCCTAC[A/G]CCTTCACTACTCACC | 10477 |
rs188822786 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031723 | ATTCCATTCCTTCTT[C/T]ACACCCATTTTTGGA | 10477 |
rs188829161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988727 | GTAATAATTGAAATA[A/G]CATGTGATCCCTATA | 10477 |
rs188858427 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059440 | TCTAGAGCAGCATTA[A/T]TGGAAATATAGTAAA | 10477 |
rs188863355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042770 | GTGCTAAGTATCTGG[A/G]TTGGAAGTAGTGATA | 10477 |
rs189007333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030315 | TTCTTTTGTATTTAT[G/T]TATTTATTTATTTTT | 10477 |
rs189035330 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001203 | AGTTCCTTTAAAGCT[C/G]TAGTGTTTTAGAAAC | 10477 |
rs189037758 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006239 | TAGTACAGAAAAAAT[G/T]CCCCAGTCAAGATTC | 10477 |
rs189043397 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056955 | TCAGCCAGACACCTA[C/G/T]TATTTCAGCCAGAAA | 10477 |
rs189046210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022926 | ACTTACAATGGGGCT[A/G]TGTCCTGATAAGCAC | 10477 |
rs189048726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983394 | TCTTAAATTTGAATC[A/G]AATCAGAGAACTGCT | 10477 |
rs189064752 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034308 | ATAGACTGGATTAAG[A/C]AAATGTGGCACATAT | 10477 |
rs189081270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991001 | AATCTGTTCCACAGT[A/G]ATGTTTCTCGACATT | 10477 |
rs189091837 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062969 | TAGCCTTTACAATAC[A/G]GACTTCTGTGTATAT | 10477 |
rs189092488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034606 | GGGTGCAGCACACCA[A/C]CATGGCACATGTATA | 10477 |
rs189103212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047303 | CTCAGGTATCATCTC[A/G]CCTTCTTACTCTGTA | 10477 |
rs189334461 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051389 | TTCTCATTTTTAATA[G/T]TCTTCTTAGAACTCA | 10477 |
rs189346427 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000243 | AGCTTTCTACAACAT[G/T]GGGTTAAGATTATTA | 10477 |
rs189366913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047945 | GTTACAGCTTCCCTC[A/G]TTAGGTCGTTTCATT | 10477 |
rs189492692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051915 | TACCTAAAATTTTGT[A/G]TCTGTTTTTAAGTCA | 10477 |
rs189502943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998178 | ACAAAAATATTAATA[C/G]CATTTCCTTTCACTT | 10477 |
rs189505165 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036471 | GTGTGGAGTTTGCAT[C/T]TTCTCCCGTGTCTGT | 10477 |
rs189510139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011860 | AGGATGGACTGTAAC[A/G]TTTTTTCCAGTTACT | 10477 |
rs189511957 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026415 | TCTCATAGACCATTT[C/T]GATTCCTGCTGGTTT | 10477 |
rs189612319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023234 | CACAGACACAAAATC[A/C]CCAAATAATGAGAAT | 10477 |
rs189622266 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035986 | TCAGTACAGTGCATT[C/T]TTCAAACAGTAAAGT | 10477 |
rs189622861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030232 | TTAATGAATACTTTA[C/T]CTACTAAAGTAATAA | 10477 |
rs189649728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056633 | CCTCTGACCCAGACA[C/T]TTCCCAACATTGCCG | 10477 |
rs189662223 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040847 | AGAGAGTTAGACTGT[A/G]CAGTAAATGAGCTAT | 10477 |
rs189806491 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978807 | CTAAATATCTTTCTC[C/G]CCTAAGCTCCTTACC | 10477 |
rs189845914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034583 | CCTAATGTAAATGAC[A/G]AGTTAATGGGTGCAG | 10477 |
rs189865792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012837 | GCATGAATTTAGAGA[C/T]ACTAACAAGTATTGG | 10477 |
rs189875629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010514 | AATCAAAGGGATATT[C/T]GCATATTTATAGATT | 10477 |
rs189876360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006510 | TAAACAATAATTTTT[A/T]TAAGTATGTCCCAAA | 10477 |
rs189890163 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035727 | TGTCATTAATGTTAG[G/T]GTATTTTATATGTGA | 10477 |
rs189891717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037225 | TGTAGTACATACTTG[A/G]TAATAAACAACTGTG | 10477 |
rs189894002 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980931 | TTCTCTCTCCCTCCC[C/T]CACACCGTAGCGGCG | 10477 |
rs189898687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027210 | CGGATTTGTAACGTA[C/T]ATATGTATGTATATT | 10477 |
rs189906104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999126 | AGTTATCTAATCTCA[C/T]TGATGAACAAGAATA | 10477 |
rs190101136 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026079 | AATGACAGTAGATTT[G/T]GGGAGGCTTTTGCGT | 10477 |
rs190104381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000500 | GTAAGTATAGTATAA[A/G]TGGTATCCCCTGAGT | 10477 |
rs190111778 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016121 | AAATACTAGTGAACA[A/G]TGTAGTGGGCCCGGT | 10477 |
rs190119443 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997381 | TTTTTCATATGACTT[A/G]TTCTGTTTCTTTTTT | 10477 |
rs190132368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040147 | AATTTATATACTTAA[A/G]TTGGGGAGGAAAATA | 10477 |
rs190138644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029603 | GTATAAATGTTCTTT[C/T]TAATTCTAATAATTT | 10477 |
rs190146683 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984407 | ACTGAAGAAACTTCT[A/G]AAATTTTGCTAAGCT | 10477 |
rs190152519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029299 | ACGCATTCATATAAA[A/T]TGAGAATCAGCTTAT | 10477 |
rs190153053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001033 | AGATTTACTGTGATG[A/T]GATGGAGAATATGAC | 10477 |
rs190181245 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055749 | GATAAGTGGGAAGAG[A/T]GCACATTTAAGAACT | 10477 |
rs190345392 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987943 | TGGTGAATTGTATAT[A/G]TAAGTAGGTTTGAAA | 10477 |
rs190349081 | snp | A/G/T | 0.000209675 | 0.010237 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984004 | GTTATTCTGTAGACT[A/G/T]TATCAAATCCTTTTT | 10477 |
rs190389227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041851 | CAGCGTGGTCTGGAA[G/T]AGCAGTGGAGTGTGA | 10477 |
rs190393442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039107 | AGTCCTAACCTCCAG[A/T]ACCTCAGAATGTGAC | 10477 |
rs190413277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015694 | GTCACTAGGAAAAAT[C/G]GACATTTAAAAAATA | 10477 |
rs190416078 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019208 | CAAGGGATCCACCTG[C/T]CTTGGCCTCCCAAAA | 10477 |
rs190566031 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061423 | CCACCGCGCCCGGCC[A/G]ACCACTTCTAACAAG | 10477 |
rs190569767 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045302 | TCCAAGGAGGCTGGC[A/G]TGCCCCTGGCTGAGC | 10477 |
rs190575444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004993 | GTCAGCCTATAAGAC[A/T]AACTCAGCACTGTGT | 10477 |
rs190579239 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033472 | TGGGAAAAGTGGCTA[G/T]CCATATGTAGAAAGC | 10477 |
rs190605754 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002667 | ATTAATGAGATATTT[C/G]ATAATTTTTTTGTAC | 10477 |
rs190649005 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030990 | TTTGTTACCTTTTCT[A/G]TTTACTTGAGCTAAT | 10477 |
rs190655806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985124 | TGTATGTTAACTGGA[C/T]CCTCAGATAAGGTGA | 10477 |
rs190666836 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979832 | ATGTTTTAGCTCTCA[A/T]CGCCACCCCCCAACC | 10477 |
rs190683066 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058986 | AGTTTTCCTGGACAC[A/C]TTTTAATGAAAAACA | 10477 |
rs190718579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016692 | GCTTTAACAACTGTC[A/G]CCCTATCAGTCTCAC | 10477 |
rs190816965 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992665 | CATGCCTGACTAACT[A/T]TTTTTTTCTTTTTGG | 10477 |
rs190818898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048367 | GAATTTGTTTTCTTT[A/G]TTGAATCTAACAAGT | 10477 |
rs190824860 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034869 | GAAAAAAATTAGAAT[A/T]TGAAAAATTTGAAGA | 10477 |
rs190826792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007262 | TTCAGAATTTTTGAG[A/C]CTAATTAAAATAGCT | 10477 |
rs190830991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986585 | GGTGATTGTACAGTT[C/T]AAATTTATTAATTTA | 10477 |
rs190834958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024079 | TCCTATTGATACTGT[C/T]GTTGTAGGTCAGGTA | 10477 |
rs190931235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032744 | ACTGATTCAGAACCA[C/T]TGCAATTTTTGGGCA | 10477 |
rs190947805 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028128 | GCATATATTGTTTAA[C/T]TTTGAGCACTATACA | 10477 |
rs190955600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004080 | TCTTGGAGAGGCTGG[A/G]GTGGAGAGTTAAGAA | 10477 |
rs190961231 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001092 | GAAACAACTTGGGAC[A/G]ATTTGCATTACTTGG | 10477 |
rs190984497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053981 | GTTCTCCCACTTACT[A/C]ATATGCATTTAAGTT | 10477 |
rs190986640 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037638 | AAGCTCAGTGTTACT[A/G]CAGAAGAATCAGAAA | 10477 |
rs191003380 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053420 | AGAACAAATTTTTGG[A/G]ACATACTCGTTTATA | 10477 |
rs191038788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989860 | GTTGCTGTAACAACA[A/G]ATGGATATGTTTACT | 10477 |
rs191150047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989573 | GCCTAGTTATTTCCT[C/T]CATACGTGCCAGTGT | 10477 |
rs191185000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009267 | ACATTATAAAACAAA[C/T]AACTGAAAATCAGTG | 10477 |
rs191196371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993276 | ATGTATATAATACTT[A/G]TTTTAACTTTATGGT | 10477 |
rs191215508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020064 | GAGTTTGACTACTGT[A/G]TTTCTTATCTGTTTT | 10477 |
rs191221197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025370 | AATTTTCACAGTGTC[A/G]TAACATTGATTTTGT | 10477 |
rs191223078 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994935 | GGAGTCAAGAGAATC[A/G]TTAATGTAAATATTA | 10477 |
rs191234876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048701 | AATTGTGAACTCCTA[A/C]TTGCTTTCAACCTAA | 10477 |
rs191254143 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024693 | AAAATTTTAGTGACT[A/G]CTTATATGCTCATCA | 10477 |
rs191387852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041779 | AAATAAGAATTATAT[G/T]TTTGGCCAGTGCTTT | 10477 |
rs191422381 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058741 | GTATATGTATATGTG[C/G]ACATAAACGGATTTA | 10477 |
rs191441558 | snp | C/T | 0.0433465 | 0.140692 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980701 | TCCCCTCCGCCTCGC[C/T]GGGAGCTCGCGCCCT | 10477 |
rs191442952 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007957 | TCTACAGGAAAAGTT[G/T]GTTAATCCTTATTCT | 10477 |
rs191455775 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012202 | CGTCAACACTTACTA[C/G]ATTAACAACACTGAT | 10477 |
rs191480033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035048 | TGGAAAAGCTACATA[A/G]TAAATATACAAGTCA | 10477 |
rs191484305 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056018 | ACTGAAAGGAACCCT[A/C/G]GCTCTTTGGAAAAAT | 10477 |
rs191487876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036748 | GTTTTTTATTAACTT[C/T]TCTTAACTGTATGTA | 10477 |
rs191635545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055198 | AGGAGTTTTGCTGTC[A/C]AGGAAAGATGATTGA | 10477 |
rs191637049 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983116 | GTATAATGTTTACAG[C/T]ATTAACCAATTTTGA | 10477 |
rs191642900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000183 | GTTCAGAATAAGACT[A/C]ACTGTATTATAAAAC | 10477 |
rs191644807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038739 | TAACATACAAGTCTT[A/G]TATCTTAATAGACAA | 10477 |
rs191647616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014388 | ATTTTAGGTGTATAG[A/G]TGGCAGTATGTATCA | 10477 |
rs191650593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028634 | CATGGTTTTAATTTG[C/T]ATTTCCTAATAATGA | 10477 |
rs191652744 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062142 | TTGCCAGGGAAAGAA[A/G]CTTCTGAGCAGTTGG | 10477 |
rs191695823 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998760 | TCAGAACGTAATAAG[A/G]TGCAACTTTGGAGGA | 10477 |
rs191745779 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001275 | AATGAGGTAAAATAT[A/G]TCACTTAATCAGGAA | 10477 |
rs191753010 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026708 | TTACTTCAGGTAGAT[G/T]TCATTACCTCGACTG | 10477 |
rs191761809 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030423 | ATGTCAGACTAACTT[C/T]GCATTTCCAATTTGG | 10477 |
rs191784304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052877 | TGTGAAATGCTTGCT[C/G]GTCACTTTTCTACCT | 10477 |
rs191796906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056974 | TTCAGCCAGAAATGC[A/G]TTACATGAATCAAAT | 10477 |
rs191844019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987116 | TTTTAAATGGTTTTA[A/G]GTATTGGAGGGCCAT | 10477 |
rs191848409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058007 | TTTCACAAATAATTT[A/G]TAATAAACAGAAAGA | 10477 |
rs191850838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041357 | TAGAAGCTTAGAACA[C/T]ACTACTTTTTATATA | 10477 |
rs191851094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001589 | AAAGTGAAGAAAAAA[A/G]TAAAGGAGATTAGGA | 10477 |
rs191857851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030543 | CTTCTTTTTTTCTTA[C/T]ACCTAATTAGCCTGT | 10477 |
rs191859151 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018511 | TATTCTTGATGAGCT[C/T]TTGTGCCCGAGGACT | 10477 |
rs191980130 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020329 | TGAGTATCTCTGTCT[C/T]TCTTCTCTTCTTGTA | 10477 |
rs192017046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044320 | ATTTAGAAACTGACT[A/T]TATGTAATTTATATA | 10477 |
rs192046583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034329 | TGGCACATATACACC[A/G]TGGAATACTGTGCAG | 10477 |
rs192051025 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017416 | GTTAGGGGCATGAGG[C/G]GGGTGGAAACCAAGC | 10477 |
rs192074178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006249 | AAAATTCCCCAGTCA[A/G]GATTCCCTTGAGCTG | 10477 |
rs192076973 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063101 | TGTTTAAAACGCCTA[C/T]TTGCAAGTCTTGCTT | 10477 |
rs192082581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023087 | TAGAAACCATAACCC[C/T]GACATGAGTAAGTTG | 10477 |
rs192090597 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047470 | TCTCATAAACTTCTT[A/C]GTCCCAGTGTATCCA | 10477 |
rs192104743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041020 | TTTGGGAGACCCAGG[C/T]GGGCGAATCACGAGG | 10477 |
rs192233352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987769 | TTTCTTCTGAGGGTT[A/G]CTACCACTTTCCATC | 10477 |
rs192247899 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035282 | AATGTATATTCCTTT[A/T]TCTGAACTATTCTTT | 10477 |
rs192293802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018833 | CATGCCTTTTATATA[A/G]GGGAGTGTTATTTTC | 10477 |
rs192300163 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035446 | AATAGTAATAACTAC[G/T]CTTACTAGTGATATA | 10477 |
rs192306295 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004547 | CTGAGGCAGGAGAAT[C/T]ACTTGAAACATGGAG | 10477 |
rs192307491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025580 | AATACCACATATTAA[G/T]TTTTTTTCTACATTT | 10477 |
rs192332738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010199 | TAGCTTTATTATTTT[A/G]TATTATTAATTGTGG | 10477 |
rs192340567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050361 | ACATCCTAAGTGCTA[A/G]AAGACTCTAAAACTC | 10477 |
rs192349225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060445 | ATTTAAGTATAACTG[A/G]TCAGTTCCTCACTTT | 10477 |
rs192496173 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005571 | GCATTATCTATTTCT[C/T]CATAGTCCTTACCTC | 10477 |
rs192537709 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034210 | ATAAATCATGCTGCT[A/G]TAAAGACACATACAC | 10477 |
rs192558959 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022493 | GTTGAAAAACATCTT[C/T]TCAGTGTATATTGTT | 10477 |
rs192600426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990871 | TACACAAGTTACTTC[A/C]ATTTTTACAAGTTCA | 10477 |
rs192603839 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005831 | AAATGGCAAGGATGT[G/T]TATAAAGGGTCAGGT | 10477 |
rs192650367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002230 | TATCACTTGTTGGCT[A/G]CATAAGAGTACTAGT | 10477 |
rs192702208 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049412 | TTTGTGTGTGTTTTT[A/T]AAATTATTTCACCTT | 10477 |
rs192732146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997382 | TTTTCATATGACTTA[C/T]TCTGTTTCTTTTTTG | 10477 |
rs192745143 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026080 | ATGACAGTAGATTTG[G/T]GGAGGCTTTTGCGTA | 10477 |
rs192759568 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051218 | TAATCCTTCAGCTTA[A/T]CTTTTTTCACTCAGC | 10477 |
rs192795733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990528 | TGCGTAGTTTACATA[C/T]GTCTTATATTATTTG | 10477 |
rs192817281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045986 | ATCCAGCATTATTTT[A/G]TGTGGATAATTTTGT | 10477 |
rs192828676 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021152 | GTGGGCTTTCACATA[C/G/T]AGTAATGTAGTTGCG | 10477 |
rs192860284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013977 | AACATGCTTCTAATA[C/G]TCTAGGAAGGATTTG | 10477 |
rs192878651 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982401 | GGTGGTATGTAAGCA[A/G]CATTACTAGAATTAT | 10477 |
rs192886870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038366 | ATCTAGCTTTGTGTA[A/G]ATACGCTATGATGTT | 10477 |
rs192943702 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010575 | ATGTAAGAAAGATGA[G/T]CTGAGTTTCACAGGT | 10477 |
rs192961165 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978851 | TCAGCAATTGGCCTT[C/T]GGGCCTTCAGGCTAT | 10477 |
rs192972052 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035798 | ATAGTTGTACTTGAT[G/T]GTTCCCAAGGGTTTT | 10477 |
rs192986183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978457 | CATTCTGCAGGCTAC[A/G]TTTCTGGCTGCCCCA | 10477 |
rs193034720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059019 | AATTGGCTAATATAA[A/G]AATTTCACACTATAT | 10477 |
rs193073398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028457 | TCTCACAGAGAACGT[A/G]CATATTCAACCATGC | 10477 |
rs193087798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054499 | ACATGAGTTTGAACA[A/G]TTTTTCATACGCTTA | 10477 |
rs193118657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999638 | CTCCCGCCCTCCACC[C/T]CTCCCAAAAAAAAAG | 10477 |
rs193130783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046993 | CACTACAGAGCACCA[C/T]ATCCTTTTTAGAGGT | 10477 |
rs193197746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997219 | TTTCTACTTATTATC[C/G]ACTATCCAGCTTCCC | 10477 |
rs193210618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042461 | ATTAGGGAAGTCCTT[C/T]TATTTATTAATTGAA | 10477 |
rs193256975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981909 | TAAGTGTGAACACTT[G/T]TGAAGCTTTTTCATT | 10477 |
rs193274062 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013631 | TTCTATAAACCTGAT[C/G]ACTGGGTTTCAAGAG | 10477 |
rs193281538 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062635 | TATTAAAATATACAT[A/G]TGATCATGTTACTTT | 10477 |
rs199514773 | snp | A/T | 0.416871 | 0.186156 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061111 | GCACAGACCACTTCT[A/T]TTTTTTTTTTTTTTT | 10477 |
rs199529205 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020926 | TTAGGGAATGGTAGA[A/G]GATAGGAAAGGGGAA | 10477 |
rs199561506 | snp | C/T | | | missense | UBE2E3 | GRCh38.p7 | 2:181060788 | TTGCTGTCTATTTGT[C/T]CCCTTTTGACAGACT | 10477 |
rs199591406 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048663 | CTCCTCTCACCCTAA[A/T]TGTCTGTATTATAGC | 10477 |
rs199596082 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030744 | TTAACTACAAGTCCC[-/A]TCTCTATATTGTATA | 10477 |
rs199613885 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026872 | CTTTGATTATTGATC[-/AT]ATAATATTTTGTGTA | 10477 |
rs199680190 | in-del | -/T | 0.040671 | 0.13668 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999601 | CATACTTATTTTTTG[-/T]TTTTTTTTCATTATA | 10477 |
rs199721038 | snp | A/C | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982121 | GCGGACCAGCGAGAC[A/C]CAGCCGCTCCAGAGC | 10477 |
rs199747887 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983573 | TTGTAAATTTTAAAC[-/T]TTTTTTTTTGACAGA | 10477 |
rs199785700 | in-del | -/TGAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041709 | CCAGAGTGCTGGGAT[-/TGAT]TACAGGTGTGATGTT | 10477 |
rs199800081 | in-del | -/ATTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982995 | GATCATTTGTTTCCT[-/ATTG]ATTGATGTTTTCTGA | 10477 |
rs199896399 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061418 | GTGAGCCACCGCGCC[C/G]GGCCGACCACTTCTA | 10477 |
rs199918333 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013480 | GTTCCTCACTGGCTG[G/T]TGGCAAATGGCCCTA | 10477 |
rs199933194 | in-del | -/AGAA | 0.0248432 | 0.108648 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060930 | GTAAATGTTATTCAT[-/AGAA]AGATCCCCATAAAAC | 10477 |
rs199943648 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061414 | AGGCGTGAGCCACCG[A/C]GCCCGGCCGACCACT | 10477 |
rs199984037 | in-del | -/TTATT | 0.029116 | 0.117091 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009548 | TTATACTAGGCTTTA[-/TTATT]TTATTTTATTAATTA | 10477 |
rs199993204 | snp | A/G | 0.000384278 | 0.0138561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057659 | ATTCATTGCTAATAT[A/G]TGTACATACTGATTT | 10477 |
rs200015432 | in-del | -/AAA | 0.0418186 | 0.138422 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000289 | CATGAATAGTGATTT[-/AAA]AAACTGTTAATCACA | 10477 |
rs200031659 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053605 | ACCCCTTGTATCTCT[C/G]CCCCTGCACAGACAC | 10477 |
rs200075756 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061422 | GCCACCGCGCCCGGC[A/C]GACCACTTCTAACAA | 10477 |
rs200139502 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022753 | ACAAAAAAAAAACCC[G/T]ACAGGTTTACAGAAA | 10477 |
rs200158863 | in-del | -/TG | 0.0333695 | 0.124785 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018360 | TAATATTTTTATCTC[-/TG]TGTGTGTGTGTATAT | 10477 |
rs200228251 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997851 | TTTAAAGCCTATTTC[A/C]GATGTTACATCTTTT | 10477 |
rs200301079 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987269 | CCCTATTTGTATTTA[-/TT]GAGAATTGTTGACTA | 10477 |
rs200341892 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022120 | AAGTAAATGGAACAT[C/T]AAACTTTGATGTCCT | 10477 |
rs200528107 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018184 | TTCTTGAATGTATAA[A/T]AAAAACAGTTATACT | 10477 |
rs200558653 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013481 | TTCCTCACTGGCTGT[G/T]GGCAAATGGCCCTAG | 10477 |
rs200566537 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041233 | GAGCAAGACTCCGTC[A/T]CAAAAAAAAAAAAAA | 10477 |
rs200580520 | in-del | -/TTATT | 0.0248432 | 0.108648 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022210 | TATGAATGTTAATAG[-/TTATT]TTATAGGAAATGTAA | 10477 |
rs200642210 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024577 | TATATGTGATTATTA[A/C]GATGTAATGGTGATG | 10477 |
rs200643146 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048228 | GTTTTATGTTTTTTT[-/T]GTGAGTTTATTTGAT | 10477 |
rs200648787 | in-del | -/TTTA | 0.0209421 | 0.100162 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031512 | ATTACTCTGTGTGTT[-/TTTA]TTTATTTAGTCTGAC | 10477 |
rs200667222 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025500 | GTGTATACAGGTATA[C/T]TTGGGATATATGGCA | 10477 |
rs200676376 | in-del | -/CTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025401 | CATTGAAGATATTAT[-/CTA]TTTTTTCCCTGACAG | 10477 |
rs200719369 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048665 | CCTCTCACCCTAATT[-/G]TCTGTATTATAGCTT | 10477 |
rs200728679 | snp | C/T | | | missense | UBE2E3 | GRCh38.p7 | 2:181060777 | TTTCAAAGGTTTTGC[C/T]GTCTATTTGTTCCCT | 10477 |
rs200731223 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061416 | GCGTGAGCCACCGCG[C/G]CCGGCCGACCACTTC | 10477 |
rs200772865 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040924 | TCTTAGAGGTTCCTT[C/G]TGATGCTTCAGCACA | 10477 |
rs200775362 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062754 | CCTTGAAGAAGATAC[C/T]ACAAAATAGCTTTTA | 10477 |
rs200807003 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018616 | TTTTTTTTTTTTTTT[-/T]CCATTAGTGAGCTGA | 10477 |
rs200827066 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003465 | TTTTGAAGAACTTCC[C/T]GGGGGGATGACGCTG | 10477 |
rs200844899 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020928 | AGGGAATGGTAGAGG[A/T]TAGGAAAGGGGAATT | 10477 |
rs200876234 | in-del | -/AAGA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006676 | TTCATATGTGGTTGT[-/AAGA]AAGAAAGCAGAGAGA | 10477 |
rs200880629 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001431 | CCCAGAAGTCCTCCA[-/C]CCCCCACACCCCCAA | 10477 |
rs200924310 | in-del | -/T/TT/TTT | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991158 | CTTTGATTTTTTTTT[-/T/TT/TTT]CTTTTTTTTCAGAGT | 10477 |
rs200999533 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053606 | CCCCTTGTATCTCTG[C/T]CCCTGCACAGACACA | 10477 |
rs201031159 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061419 | TGAGCCACCGCGCCC[C/G]GCCGACCACTTCTAA | 10477 |
rs201035065 | in-del | -/A | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990278 | GGTAGACGTCAGTGG[-/A]TACTGCTGAATACCC | 10477 |
rs201090271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998134 | CAACTGTGCTTGACC[A/G]TACTCCTTGGTTTAC | 10477 |
rs201090684 | in-del | -/TTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018599 | GTTTCAATTTCTGTG[-/TTTTT]TTTTTTTTTTTTTCC | 10477 |
rs201137250 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058453 | ATCAACTTTGCAAAG[C/T]TTAAATATAACAATT | 10477 |
rs201205258 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018491 | CCTTTCAGTGCAGTT[-/A]AATCTATTCTTGATG | 10477 |
rs201212158 | in-del | -/AG | 0.0460142 | 0.144533 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985886 | GTATTAAGTGCCCTC[-/AG]AGCAATAGCCTAGTG | 10477 |
rs201218005 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029568 | TTTATCTAAAAACTT[-/G]TTTTTTATCTAGCAA | 10477 |
rs201222189 | in-del | -/GA | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992881 | TGTTGATCAGGCTGG[-/GA]GATTTGCTTTTTCCA | 10477 |
rs201270976 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022874 | TGCAAAAGCCCCTAG[G/T]ATTGATTTTTGGCTT | 10477 |
rs201317699 | in-del | -/TTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029660 | TATCTGTAGACAATC[-/TTTT]TTTTTTTTTTTTTTT | 10477 |
rs201325793 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004122 | TGTGAAGTTAAATTT[-/A]ATCAGTACAGCATAA | 10477 |
rs201327764 | snp | A/G | 3.31653e-05 | 0.00407204 | missense | UBE2E3 | GRCh38.p7 | 2:181060761 | AGTCCCGCTTTGACT[A/G]TTTCAAAGGTTTTGC | 10477 |
rs201442655 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022722 | TACTAAGTAGGCTGC[-/A]AAAAAAAAACAAAAA | 10477 |
rs201457866 | in-del | -/TTCCT | 0.0410537 | 0.137264 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021490 | CTTTCTCTCTCTCTC[-/TTCCT]TTCCTTTCCTTTCCT | 10477 |
rs201481804 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041234 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 10477 |
rs201576031 | in-del | -/TTG | 0.0174175 | 0.0916809 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028120 | ACTAAACGGCATATA[-/TTG]TTTAATTTTGAGCAC | 10477 |
rs201578060 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025501 | TGTATACAGGTATAT[C/T]TGGGATATATGGCAT | 10477 |
rs201627761 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992541 | GGGCAGCTCTTCTCT[C/G]TGTTGACTTATATCT | 10477 |
rs201672821 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060260 | GATGTAACTTTTATG[-/T]TTTAAAAAAAAATCT | 10477 |
rs201710192 | in-del | -/TATGTAG | 0.0244538 | 0.107838 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037208 | CAGCAAATATAATTA[-/TATGTAG]TACATACTTGATAAT | 10477 |
rs201755863 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016240 | TTTTTGGGGTTTAAA[-/T]TTTTTTTTTTAAATT | 10477 |
rs201868564 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061417 | CGTGAGCCACCGCGC[C/T]CGGCCGACCACTTCT | 10477 |
rs201918487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024937 | CTTCACATCAGCTCT[A/G]TTAATAAAAGTAGAA | 10477 |
rs201983173 | in-del | -/GGGA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041704 | GCCTCCCAGAGTGCT[-/GGGA]TTGATTACAGGTGTG | 10477 |
rs201984172 | snp | C/T | 0.000261085 | 0.0114225 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060855 | ATAAGACTACAAAAA[C/T]GAGTGCTTTTTTTTT | 10477 |
rs201998477 | in-del | -/TTTT | 0.283684 | 0.24772 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007501 | AACTAAGTATAATTG[-/TTTT]TTTTTTTTTTCTTTC | 10477 |
rs202091614 | in-del | -/CA | 0.0205511 | 0.0992634 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978517 | ACCCATGTTTCACTC[-/CA]GTTTCCCAAGCAGTT | 10477 |
rs202130074 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058728 | ATGTAGCCTGTGTGT[A/G]TATGTATATGTGCAC | 10477 |
rs202133995 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007515 | CCAAGTATAAAGAAA[A/G]AAAAAAAAAAAAAAC | 10477 |
rs202136166 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028639 | TTTTAATTTGCATTT[A/G]CTAATAATGAGGTTG | 10477 |
rs202150385 | snp | G/T | 0.000116638 | 0.00763581 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987328 | CATTTACTTTCCATC[G/T]GTTTCCCAGAGGGTG | 10477 |
rs202151923 | in-del | -/ATAGTTAAATGTACACTTTGTCCT | 0.138886 | 0.22395 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055672 | ATTTACTATCCTGCA[-/ATAGTTAAATGTACACTTTGTCCT]ATAGTTAAATGTACA | 10477 |
rs202154522 | in-del | -/T | 0.284733 | 0.247575 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997111 | ACACTTTTTTTTTTT[-/T]ACCCTTCTAATCTCT | 10477 |
rs202161852 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060272 | ATGTTTTAAAAAAAA[C/T]TCTTCATCAGTTCCT | 10477 |
rs202209429 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061420 | GAGCCACCGCGCCCG[A/G]CCGACCACTTCTAAC | 10477 |
rs202211026 | in-del | -/T/TT | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017662 | TCCATTTTTTTTTTT[-/T/TT]AATACGGAAGTGTCA | 10477 |
rs367615411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993608 | CCTTTACATCCATGC[A/G]TCTCACTTTTTATAA | 10477 |
rs367713784 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997080 | TTGTGTTCTTAAAAG[G/T]ATTTCTGTTACCCCA | 10477 |
rs367724096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009120 | AGCCAGTTCTTCTAC[A/G]TTTTGTCACTTGTCC | 10477 |
rs367736591 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030966 | GTTTCACTAGTTTAT[A/G]CTATTACGTTTGTTA | 10477 |
rs367737896 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029434 | CATACTGTATCACCC[C/T]CATTTATTTAGGATT | 10477 |
rs367865555 | snp | C/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055865 | ACCAACAAGTAATTA[C/G/T]GAGTTTAGATTTTAT | 10477 |
rs367930818 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037678 | AAATTTTAAGTTGAC[A/G]TAGTAAAAAAGTTAC | 10477 |
rs367936866 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055159 | GAGAGAAACTGAAGA[C/T]AGCAGATGTAGATAA | 10477 |
rs367993333 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014201 | GGAAGTTTTAGTTTT[G/T]GTTTTCAATGGTTGT | 10477 |
rs368111262 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011273 | CAGGACCTTCTTTCT[A/G]GGATGCTGCTTATCC | 10477 |
rs368124852 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059146 | TTTAGTGTTCACTCT[G/T]TTGCTGAGATATACA | 10477 |
rs368139257 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040739 | CACTTTTTAGTAGCT[A/G]TGGTATTCAAAATAA | 10477 |
rs368145278 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043339 | GCCAGTCAACCAGAT[C/T]GTCCACATGAGTGGC | 10477 |
rs368244759 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003533 | TTATTTGATATAAAT[G/T]AAGATGTAGTTAGTT | 10477 |
rs368290754 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990728 | CTATTATGTTCTACT[A/G]GGAGTACTAAAGTAA | 10477 |
rs368302430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054988 | GGAGGATGTGATTGG[C/T]TGTGTCAAATGTTGC | 10477 |
rs368345552 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025397 | TGTCATTGAAGATAT[-/C]TATCTATTTTTTCCC | 10477 |
rs368404118 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034044 | AGGTGCTGGAGAGGA[C/T]GTGGAGAAATAGGAA | 10477 |
rs368510934 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988290 | ATTTTATCTTAGTCA[A/G]TTCACCAGATAATTG | 10477 |
rs368519318 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047249 | ACACCTGTTAGAGGT[C/G]TGACATGTATTATTG | 10477 |
rs368523342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050691 | GAATCTTAGCTCTGC[A/G]TATACGACCCTAGGC | 10477 |
rs368596633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039408 | CAGACGAGCATTCTG[C/G]CTCCTGGAGCGGCTG | 10477 |
rs368612608 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996384 | TGCTTTAAGTTTTGA[A/G]TTAAACTGAGGGGGT | 10477 |
rs368632912 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060622 | GTTTTAATTGGTAAT[A/G]CAGCATTCATTTTCC | 10477 |
rs368730857 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047420 | GCCCCTTTATCTTAC[G/T]TGTCTGTCTCTTTGA | 10477 |
rs368764123 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045036 | GTATACCTTGTGTTT[A/G]TGCTTTTACGTCTGC | 10477 |
rs368776230 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997458 | TACTTGAAATGTGTC[G/T]TCTTTCTCCCACTCT | 10477 |
rs368783090 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012629 | AAGCCGGTTTGGAAT[C/G]TCTGACTGAGTAAAA | 10477 |
rs368818008 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028898 | CTCTTATATGATTAG[C/G]ACTTTTTGTGTCATG | 10477 |
rs368841456 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036513 | CCGTGTATTCTGGTT[C/T]CCTCCTAAATTTCAG | 10477 |
rs368852650 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012342 | TTGGTTAGTTACAGT[G/T]GTCATTTGAATCAGT | 10477 |
rs368864126 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984653 | AAGCAAATGTCCTAA[C/T]TGCTTGGGAACATTT | 10477 |
rs368894473 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031398 | ATCTTTGCTGTATTA[C/G]TATACCTTGAGGCTA | 10477 |
rs368908672 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025052 | AAGCCTTTCATGTGG[C/T]TTTAGTTAGCCACAT | 10477 |
rs368917272 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006920 | AGAGTAAAATTACTT[C/T]AAAAGCCATGCAGAA | 10477 |
rs369023180 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034711 | TTTCCTGGAACTAGC[A/G]TGTCAGAATACCATT | 10477 |
rs369058192 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059678 | ATTCACCTTGCCACA[A/G]TTTAAGAGCTGTATA | 10477 |
rs369195598 | in-del | -/GA | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996392 | GTTTTGAATTAAACT[-/GA]GGGGGTAGTTTAAGG | 10477 |
rs369278728 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040840 | TAGATCCAGAGAGTT[A/G]GACTGTGCAGTAAAT | 10477 |
rs369282760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039623 | CAAAAAAACAAGTGT[A/G]CAAATGCTAATTTTG | 10477 |
rs369393313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041663 | GGCTGGTCTCGAACT[C/T]CTGACCTTATGATCC | 10477 |
rs369398757 | in-del | -/TATAGTTAAATGTACACTTTGTCC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055695 | ATGTACACTTTGTCC[-/TATAGTTAAATGTACACTTTGTCC]GATGGCAAATAGCAT | 10477 |
rs369437711 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980133 | ACACCCATTAGTCTC[C/T]CGTCTCCCGGGGCGG | 10477 |
rs369490208 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061608 | AAAATGATAGCCAAT[A/G]AGAATTGAACTAGAT | 10477 |
rs369503431 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007031 | ATCTCTGAGCAGGTA[A/T]TATTTTGAACCATTC | 10477 |
rs369587501 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993902 | GATTTATTCTTGCCT[C/T]ATACTTGTTTCTTAG | 10477 |
rs369605332 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006276 | GCTGGCATTAGGTTT[-/A]AGGCCATAGAGTTTG | 10477 |
rs369607061 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056191 | ATCAAAATAATTAAA[C/G]TCAGTAATGACTTAT | 10477 |
rs369705370 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042157 | TCTTAAGTCTACCCT[A/G]TCCCCATCAGTCATT | 10477 |
rs369750774 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032644 | CTAAGAAAAATTTAC[C/T]ATCTCTTTGAAACAC | 10477 |
rs369775226 | in-del | -/TCCTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021506 | TCCTTTCCTTTCCTT[-/TCCTT]CTTTCTTTTATTCTT | 10477 |
rs369780505 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017245 | TACATTAAAGTGGGA[-/T]TACAGTGGTCAAGAC | 10477 |
rs369939558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046224 | TCTTCCATAAAGCCA[A/C]AGATAAGCAGGAAAT | 10477 |
rs369989942 | snp | A/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984930 | ATAGTTTGTGAAGAG[A/G/T]TATGTGCTCAATAAT | 10477 |
rs369994693 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048131 | AATAATCTTTTAAAT[A/G]TTGCTTCCTCTGACT | 10477 |
rs369996840 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007295 | CTACCTTATCCTTTT[A/C]CCTCATCTGTACAGT | 10477 |
rs370011064 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011302 | CCCATGGCAGAGTTC[A/T]AGAGAGAGAGGTGAT | 10477 |
rs370053986 | snp | A/C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016039 | AGCTTTATAAAGTTA[A/C/T]AGGAAATTTTAGAAA | 10477 |
rs370058301 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034595 | GACAAGTTAATGGGT[A/C/G]CAGCACACCAACATG | 10477 |
rs370079391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033335 | ACCAAAACGGAGATA[C/T]AGACCAATGGAACAG | 10477 |
rs370079489 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013831 | AAGGGAGCAGAAATA[G/T]ACCATGCCTCTTCAT | 10477 |
rs370101423 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046265 | AATTTTGAGTCTTTC[A/G]CAGGTCAGGGATTCC | 10477 |
rs370133264 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983992 | TGTAATTCCCTGGTT[A/G]TTCTGTAGACTATAT | 10477 |
rs370184291 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008027 | CTTTGTATTCTGAAT[G/T]GTCTTTTTAATCTGG | 10477 |
rs370331757 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998906 | TGTTTGTAAAATAAC[-/T]TTTTTCAATTTATAC | 10477 |
rs370356418 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049590 | ACTGTCATAATAGGC[C/G]TTAAGATAGACAAAG | 10477 |
rs370441269 | snp | C/T | 3.32696e-05 | 0.00407844 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057679 | CATACTGATTTTTAA[C/T]TTCTTTTAAATAGTG | 10477 |
rs370471154 | snp | C/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022711 | CAAAAAGCATGGTAC[C/G/T]AAGTAGGCTGCAAAA | 10477 |
rs370481167 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008410 | AGCAAGATTTGAAAT[C/T]AGGCAGTCTGGCTCC | 10477 |
rs370485228 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992333 | AATTCTTAAACACAA[A/G]TATTAAGTAATACTT | 10477 |
rs370597201 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000080 | GTTTCCAGCTGCCTT[C/T]TGCAATTTTTGTTCT | 10477 |
rs370607861 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027270 | TCTTTGACTAAAAGA[C/T]GGACCTCAACAAGTG | 10477 |
rs370709061 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024080 | CCTATTGATACTGTC[A/G]TTGTAGGTCAGGTAA | 10477 |
rs370784592 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045230 | GATCAATTTTAAAAA[A/G]CTGTTATATTATGCT | 10477 |
rs370795153 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996076 | GTAGTACTTCAGTAT[A/G]TTGCTGTTATCATCT | 10477 |
rs370833987 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020332 | GTATCTCTGTCTCTC[-/TT]CTCTTCTTGTAAGGA | 10477 |
rs370869282 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979253 | ACACAGCAATTGAAT[A/G]AGTGTATGTCCAGCA | 10477 |
rs370912145 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047320 | CTTCTTACTCTGTAC[G/T]CTTTACCTAGCCTGG | 10477 |
rs370934566 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057199 | TATTACCGAATCAGT[G/T]GACAACATTATAATA | 10477 |
rs370997129 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045841 | GAGCCAGTGTTAACT[G/T]ATGGGAATATACACA | 10477 |
rs371084893 | in-del | -/ACTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040109 | TTAAGTGGCCATTTG[-/ACTG]TTTCCTTGACATTCC | 10477 |
rs371087447 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044595 | TACTGTGTAGAAACT[A/G]CTTTTTGTAATTTCA | 10477 |
rs371103691 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984037 | CTCTTCTCATTTCAC[A/T]AACAGAATTCAGAAG | 10477 |
rs371112864 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057477 | ATACCAATTTTCTTT[A/G]TACTTTTCTTGCATT | 10477 |
rs371160952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049087 | TTTCAGCTGAGGGAG[C/T]AAAGAAGCTTCAGAG | 10477 |
rs371358319 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017245 | TTACATTAAAGTGGG[A/T]TACAGTGGTCAAGAC | 10477 |
rs371362973 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000423 | TCTAAAATGTTAACA[C/T]TGTACAACTCCAGGG | 10477 |
rs371500664 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979803 | AAGACAGAAGAGTCC[C/T]GCAGAAAAGTGTCAT | 10477 |
rs371502594 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038312 | AGCCTGGGAGCAATA[A/G]GCTATACCATATAAC | 10477 |
rs371506491 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982725 | TAAAATTGTGCTGCA[A/C]ATCTGCTTACAGTTT | 10477 |
rs371512683 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029445 | ACCCTCATTTATTTA[A/G]GATTTCTTTAATTCT | 10477 |
rs371539531 | snp | A/T | 1.65679e-05 | 0.00287814 | missense | UBE2E3 | GRCh38.p7 | 2:181057796 | CTGGATATCACATTT[A/T]CATCAGATTATCCAT | 10477 |
rs371549264 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041480 | GAGTCTCTCTCCGTC[A/G]CCCAGGCTAGATTGT | 10477 |
rs371549449 | in-del | -/ACT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049895 | CTATGAAATACTACT[-/ACT]TTTCTGTAGGCCATG | 10477 |
rs371595317 | snp | A/G | 1.72928e-05 | 0.00294043 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181062792 | TTCTGCTTTTCCAGC[A/G]GATCCTCTGGTTGGA | 10477 |
rs371599300 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048155 | TCTGACTCTTCCCTT[A/G]TCTCTCTAACATTTC | 10477 |
rs371620676 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043155 | GAAATGCTCCAAGAC[A/G]TGAAACTTTTTGAGT | 10477 |
rs371626169 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020569 | GAATTATTTCCTTTG[A/T]TTTTAATTCATAGTC | 10477 |
rs371640455 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042567 | AGTTTTCTAAGGATG[C/T]TGGTGAAAGAGTGCC | 10477 |
rs371641795 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010682 | AAACAGTGTTTTCTG[G/T]TGGGACTTCAGAATA | 10477 |
rs371737850 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006103 | AATTGGGAGGCATTT[C/T]CAGAGTCTCTTACTC | 10477 |
rs371755295 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051615 | ATTGTGGGAAAAGTC[A/G]TATCAACATTAGGAA | 10477 |
rs371873857 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011437 | CTCCCGCAGCCCAGT[A/T]ACCTCTCAGAGGTTC | 10477 |
rs371903441 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043408 | TCTGTTTCATGCACA[A/G]AATTATTTAAAATAT | 10477 |
rs371921707 | in-del | -/GGC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013506 | CCTAGTTTCTTGACT[-/GGC]TGTTGGCCTACCTGT | 10477 |
rs371924755 | snp | C/G | | | upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980294 | GCCCCGGAGGCGGGC[C/G]CAGGCCGGAAGCCAC | 10477 |
rs371937611 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019853 | TTTTTTTTGTGGTGA[G/T]AACATTTAAGATCTA | 10477 |
rs371945609 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997643 | ATCAAAAGTACCTGC[A/G]TTTAGCTCTCTTAAT | 10477 |
rs371952287 | in-del | -/AAATGGCCCTAGTTTCTTGACTTGTTGGC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013485 | TCACTGGCTGTTGGC[lengthTooLong]CTACCTGTAGGCTGC | 10477 |
rs371999304 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036612 | GTTATGTGAAAGTGT[G/T]CCCAGTGATGCAGGA | 10477 |
rs372001058 | in-del | G/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021363 | TTTTCTCTTCTTTTT[G/TT]TTTGTTTTCTTTTCT | 10477 |
rs372013461 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058486 | TTGAATGGCTCCCTC[C/T]GCTAACTTCTGTTTC | 10477 |
rs372020445 | snp | C/T | 8.27876e-05 | 0.00643327 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181060727 | AGTCATCTGTCTGGA[C/T]ATCCTTAAAGACAAC | 10477 |
rs372074953 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001462 | CTGTGAATGTAGAGG[-/G]TGGGACATCAAGAAG | 10477 |
rs372130948 | snp | A/C/G | 0.0142736 | 0.0832652 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037744 | GAGGTTAAGGGGGGA[A/C/G]GATTATTTGAGGCCA | 10477 |
rs372168905 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999797 | AGCAAGTTATCTCCT[C/T]TGATTCTCAGAAATG | 10477 |
rs372238472 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025398 | TGTCATTGAAGATAT[C/T]ATCTATTTTTTCCCT | 10477 |
rs372255953 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015257 | AGCATTTATGGCCCA[A/G]TATTTTAAGCCTACA | 10477 |
rs372373335 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061593 | GTAGTAATGGATATT[-/A]AAATGATAGCCAATG | 10477 |
rs372379504 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984209 | CTTCTTTACAGCTTT[A/G]CAAGTGCATTAAACA | 10477 |
rs372510255 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027654 | AGCAAGAGTGCTGCA[A/G]CATGTTGTGTCTTTT | 10477 |
rs372598354 | multinucleotide-polymorphism | GC/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056035 | CTCTTTGGAAAAATG[GC/TT]TGATTCCAAGGATGG | 10477 |
rs372660479 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001436 | AAGTCCTCCACCCCC[A/C]ACACCCCCAACTGTG | 10477 |
rs372695414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034323 | AAAATGTGGCACATA[C/T]ACACCATGGAATACT | 10477 |
rs372752487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036080 | AAGGACTTGGCTCAC[A/G]GCAGGCAACAGGCAA | 10477 |
rs372762079 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019838 | CTTTTAATTTTTTTC[C/T]TTTTTTTGTGGTGAG | 10477 |
rs372781641 | in-del | -/CA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042662 | GCAAGCACCTGACCT[-/CA]GTTTCCTCATTTGTA | 10477 |
rs372999598 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991160 | TTTGATTTTTTTTTC[C/T]TTTTTTTCAGAGTTT | 10477 |
rs373023448 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022207 | TTTTATGAATGTTAA[C/T]AGTTATTTTATAGGA | 10477 |
rs373047568 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995940 | TCATACATGGTAAAG[A/G]TAAGATATGTGCTTA | 10477 |
rs373058602 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056818 | AGGGAAAAGATAGTA[A/C]CTAAGCAGTAGGAAA | 10477 |
rs373064254 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036105 | AGGCAACATCTTGTA[C/T]ATTCTAATTTTTGCA | 10477 |
rs373112500 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037595 | AAGGAAAATATTTTT[A/G]TACAGCTATACACTG | 10477 |
rs373112879 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004525 | GTAGTCTCAGCTACT[C/T]GGGAGGCTGAGGCAG | 10477 |
rs373119518 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985579 | CTATTGAACAGTGCC[A/G]CTTTAGAGAACAAGT | 10477 |
rs373139588 | snp | C/T | 1.65869e-05 | 0.00287979 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982125 | ACCAGCGAGACCCAG[C/T]CGCTCCAGAGCCTGA | 10477 |
rs373154039 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023910 | TCATTACTACTATTA[G/T]TATTATCCTTAATTT | 10477 |
rs373198146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016117 | AAATAAATACTAGTG[A/C]ACAATGTAGTGGGCC | 10477 |
rs373212312 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040170 | GGAAAATATGTTTGC[A/G]TTCTTCTTAGTGGAT | 10477 |
rs373226569 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039324 | AAGCTGATTAAAAAC[A/G]TTTGAAAAATACAAT | 10477 |
rs373228298 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017503 | GACAATTCTGAGCAG[G/T]TTTCTCCAAGGGAAG | 10477 |
rs373276108 | snp | C/T | | | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989937 | ATTGAGAATGAAGAA[C/T]TTGTCCTTTCAGTCT | 10477 |
rs373332374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023687 | ATAGAGTCCATGCTC[C/T]CAACCCCTTTGCTAT | 10477 |
rs373337708 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989210 | CTAATAGTTTCTTCA[A/G]CACAACTGTAATAAA | 10477 |
rs373354537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994475 | AGTATTTCACTATGC[A/C]CTTTCAAAAGATAAG | 10477 |
rs373457867 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985412 | ACAAAAGGATGTATA[A/G]TACTGCATTGACTTA | 10477 |
rs373465696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022150 | TATGATTAATATTGT[C/T]ATGGCAAACATACTA | 10477 |
rs373512574 | in-del | -/TGCTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060859 | GACTACAAAAACGAG[-/TGCTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs373524979 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985997 | GAGTAGAATCTTTCA[A/G]TGAGATAGGAGGTTT | 10477 |
rs373555892 | in-del | -/AAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039282 | TTCAAAATGGTGAAT[-/AAA]TTTTATAAATAAATT | 10477 |
rs373556560 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042733 | CAATTCTGAACATCC[A/G]TAATTGAGTCCCAGG | 10477 |
rs373587701 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012425 | TTAATAGCTCTTTAA[A/G]TTAAAGAATGTCAAG | 10477 |
rs373591055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058226 | AAGGGTTTAATAATG[G/T]GAATTTTGTGCTGAA | 10477 |
rs373599785 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035211 | TTGTAAAAAGTGAAA[C/T]CTACAAAGTAAAACC | 10477 |
rs373601935 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049139 | ACCATTAGCAGAGAA[A/G]TCAAGGATCTGCTGG | 10477 |
rs373704258 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046984 | TTTCCTTTTCACTAC[A/T]GAGCACCACATCCTT | 10477 |
rs373802159 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996054 | CATAATTGTATTTCA[A/T]CCCATTGTAGTACTT | 10477 |
rs373803175 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986577 | AGCTTTACGGTGATT[A/G]TACAGTTTAAATTTA | 10477 |
rs373809867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048315 | CAGATTCCTAGCCCC[A/C]AATCGTAGACACTCA | 10477 |
rs373843346 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027472 | ATAAAAAGATCCCAG[A/G]AATTCTTAGATGTAA | 10477 |
rs373854990 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046329 | CACAAAACACAAATA[C/T]TTGCTAGCAGAAGAT | 10477 |
rs373883235 | in-del | -/GAATGGTAGAGGATAGG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020916 | GTTTTTAGAGTTAGG[-/GAATGGTAGAGGATAGG]AAAGGGGAATTTTTA | 10477 |
rs373920291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012218 | ATTAACAACACTGAT[C/T]AGTTTCAGTAAATGT | 10477 |
rs373926697 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983059 | CTTATCAGTGGTAGT[A/G]GTAGTGGAATATCCA | 10477 |
rs373974600 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058815 | AACAAGGTAACGAGT[A/G]CCATCTAGTGGTATT | 10477 |
rs374125049 | snp | A/T | 3.46284e-05 | 0.00416089 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984112 | AGAAATGAATTTTGT[A/T]GTTTTGGTTTCAAAT | 10477 |
rs374162599 | snp | A/G | 1.66893e-05 | 0.00288867 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057665 | TGCTAATATATGTAC[A/G]TACTGATTTTTAATT | 10477 |
rs374188230 | in-del | -/GT | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992543 | GCAGCTCTTCTCTGT[-/GT]TGACTTATATCTGTG | 10477 |
rs374213324 | snp | A/G | 1.69178e-05 | 0.00290837 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060840 | TTATTAACATGTACA[A/G]TAAGACTACAAAAAC | 10477 |
rs374387406 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035260 | ATTTGCATGATGTAA[G/T]GCTATAAATGTATAT | 10477 |
rs374416723 | snp | A/C | 6.65082e-05 | 0.00576625 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057682 | ACTGATTTTTAATTT[A/C]TTTTAAATAGTGCTG | 10477 |
rs374434100 | snp | A/C | 1.67108e-05 | 0.00289052 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057847 | AGCTTGAAGTGCATT[A/C]TTTAGTATTTAATCC | 10477 |
rs374434754 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005386 | TATATTATATCCATA[C/T]GGTTCATGCCTAGGC | 10477 |
rs374518565 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991030 | TACTGTTTCCACACC[-/A]AAAAATGTATTAATA | 10477 |
rs374547738 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013416 | GAGATTGGAAGATCT[A/G]TTTTCAAGGTGGCTC | 10477 |
rs374553477 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985216 | AGGAAACATGAATGT[A/G]AACTAATTTTAAGGA | 10477 |
rs374554739 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986202 | AAATGACATCTTTCA[G/T]TTCTCAGGTTCTTTT | 10477 |
rs374569245 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054549 | TGGTGTGAGGTATCT[A/G]TTCAGGTATTTCACC | 10477 |
rs374713759 | in-del | -/TTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029660 | TATCTGTAGACAATC[-/TTT]TTTTTTTTTTTTTTT | 10477 |
rs374821810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018512 | ATTCTTGATGAGCTT[A/T]TGTGCCCGAGGACTC | 10477 |
rs374998978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011184 | TAATGGAATGCCTGA[C/G]ACAGTAATTTATAAT | 10477 |
rs375029105 | snp | C/G | 1.69568e-05 | 0.00291172 | utr-variant-5-prime, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982022 | CTCTTTAAAAGTTTT[C/G]CAAGAGATAACTTCA | 10477 |
rs375047306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993666 | GTTATTTGTAGTTAG[A/T]TTTGCCATTTACAGT | 10477 |
rs375067635 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025141 | AATTTATAGGGGCAC[A/G]AGTGGTTTGAAGTAC | 10477 |
rs375079779 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026160 | GAAAAGATGAAAAAA[A/C]ACACTGAAACCCTTT | 10477 |
rs375084002 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045616 | GCCCCAGACTAATAC[A/G]TCAGAATCTCTAGGG | 10477 |
rs375294490 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996650 | CCCCCATTTCCAGGT[A/G]TCTTGGAGGGGAGGG | 10477 |
rs375296521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008522 | TTCTAGTTCTGGCTG[A/G]GGTCCAACTGGATAT | 10477 |
rs375318991 | snp | A/C/T | 0.000171541 | 0.00925983 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981996 | ACATTTTCTCCTCCT[A/C/T]CTCCCCTGTTCTCTT | 10477 |
rs375334518 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017135 | ATAGAAGGGCCTGAG[A/G]CTGATAGAACATTCC | 10477 |
rs375335599 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010113 | AACCAGAAACAAAGT[A/T]AGATGAAAGTCCACC | 10477 |
rs375366660 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056596 | TGAGGGAGGGCATTA[A/G]TTTATTCATGAGGGA | 10477 |
rs375416746 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015577 | ATTCTTGGAAAAATG[A/T]ACAGTTTTCATTATA | 10477 |
rs375423737 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988233 | TAGTGATGTGCTCTC[A/G]CTGTTGCTGGCATTT | 10477 |
rs375466991 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043765 | GTTTACACAATATGA[G/T]TACTGGTGTGTATGT | 10477 |
rs375473485 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023223 | GTAGGTGAATTCACA[A/G]ACACAAAATCCCCAA | 10477 |
rs375573781 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032188 | AAAATTAACTTTTTT[-/T]GTTGAAGTAGTGTGT | 10477 |
rs375619336 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022488 | TTTCTGTTGAAAAAC[A/G]TCTTCTCAGTGTATA | 10477 |
rs375634384 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037906 | CCAGGAGTTCAAGAT[C/T]GCAGTGAACTATGAT | 10477 |
rs375651531 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984798 | AGATACATTAAAAGT[A/T]GCTGGTTGATTATTT | 10477 |
rs375653770 | snp | C/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992919 | TCTTTGGAAGAGTGG[C/G]TGCTCCACTTTACAA | 10477 |
rs375695195 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018231 | CCAATAAAATATAAA[G/T]AACACTAATTATGTT | 10477 |
rs375704407 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040917 | AGTAGACTCTTAGAG[A/G]TTCCTTCTGATGCTT | 10477 |
rs375723726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049336 | TTTATCCTGGCATCC[C/T]AGTGCCTGGTCCATA | 10477 |
rs375755321 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059675 | TCAATTCACCTTGCC[A/G]CAATTTAAGAGCTGT | 10477 |
rs375790930 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040306 | TCTCTAGTTCTGCAC[-/AT]GTTACACTGTATTGC | 10477 |
rs375806785 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002950 | GAAAGAAAACTCAAC[A/G]CCCGGTACAAAAATG | 10477 |
rs375807148 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028356 | TTGTCACTATGAACA[A/G]TCGTACTGTGAAGAT | 10477 |
rs375873832 | snp | A/G | 3.54541e-05 | 0.0042102 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062892 | TACGCAACATAATTC[A/G]CATAATTTGTATGCA | 10477 |
rs375925684 | in-del | -/TACT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019639 | TTTTTTTAAAAAGTC[-/TACT]TACTATTAGTTTTTT | 10477 |
rs375958956 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039589 | CATCCTGAGCAACAT[C/G]GCGAGACTCCCATCT | 10477 |
rs375959372 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007114 | GACCTAAATTTAATC[A/G]TTTTTTTTTCCAGTA | 10477 |
rs376006819 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025400 | TCATTGAAGATATTA[A/T]CTATTTTTTCCCTGA | 10477 |
rs376186535 | in-del | -/CTG | | | intron-variant, cds-indel | UBE2E3 | GRCh38.p7 | 2:180991720 | TGGCCCAAGAGAGTT[-/CTG]CTGCTGCTGCTGTGG | 10477 |
rs376249018 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007328 | GTAGTATGGCCTGGG[A/G]AGAAAGAAGGCTAGC | 10477 |
rs376253713 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991428 | ACTCTTGGGCTTTGG[A/G]GCCATTGTTAAGTAA | 10477 |
rs376263138 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003788 | TAATTGCAGCTATAC[A/G]TGCCCATTTGAATAT | 10477 |
rs376264501 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022457 | ATTATGTAAATTAAT[A/G]CATAACCATTTTATG | 10477 |
rs376321400 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037726 | TAATGCCAGCACTTT[C/T]AGGAGGTTAAGGGGG | 10477 |
rs376327545 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039282 | TTCAAAATGGTGAAT[-/A]AATTTTATAAATAAA | 10477 |
rs376335179 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034036 | GAAACAACAGGTGCT[A/G]GAGAGGACGTGGAGA | 10477 |
rs376376145 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987236 | TGAGAGTCAAGGGAA[A/G]TTGTGTTATGGGCAT | 10477 |
rs376401200 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041325 | TTACCTCTCCTCATA[A/G/T]GGGCATTGAACAGTA | 10477 |
rs376408250 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019867 | AGAACATTTAAGATC[C/T]ACTTTCTCAGCAAAT | 10477 |
rs376453896 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005703 | TGAATAATTTGTTAC[A/G]GTTATATAGTTATAT | 10477 |
rs376460663 | in-del | -/CCTTCCTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021578 | CTTCCTTCCTCCCTC[-/CCTTCCTT]CCTCCCTTCCTTCCT | 10477 |
rs376467611 | in-del | -/GG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031280 | GTTCATTTATTATGT[-/GG]TTCAGATATTCTGTA | 10477 |
rs376487905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038351 | GTAGTAGGCTGTACC[A/G]TCTAGCTTTGTGTAA | 10477 |
rs376544269 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032458 | GAACCTCTGTAGTAG[A/T]TAGCGTGGATAAGAT | 10477 |
rs376584542 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012076 | ATTAGGTTGGAAGGA[A/C]ACAAGTTAATTGATG | 10477 |
rs376745602 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032719 | TATTAAATATGCCTC[C/T]TTATTCCCAACTGAT | 10477 |
rs377040309 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027709 | AGCCCAAATTCTCTC[C/G]TAGTGTCGTTTTTAA | 10477 |
rs377090301 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008253 | CAAATAATTCTGCTA[A/T]TATTTATTGACCAAT | 10477 |
rs377117174 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043598 | CATTTTGGATGAGGG[A/C]TACTTAACCTGAATT | 10477 |
rs377144902 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038107 | TACGCCTTCACTACT[C/G]ACCCCTGACTCACCC | 10477 |
rs377151189 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992641 | GCTGGGACTACAGGC[A/G]CACCCCACCATGCCT | 10477 |
rs377162720 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022893 | GATTTTTGGCTTACA[A/G]ATACCAGATGTCCTT | 10477 |
rs377237027 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040686 | ATCATAGGTAAAAAA[-/A]TACTGGAAAAACAGT | 10477 |
rs377263289 | in-del | -/GAGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020315 | GGCTGCCTTCTTCCT[-/GAGT]ATCTCTGTCTCTCTT | 10477 |
rs377269059 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988828 | CTTCTTTACTTAATA[C/G]ATTTGATTGTTTTTG | 10477 |
rs377319832 | snp | A/G | 1.88585e-05 | 0.00307065 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062913 | TTTGTATGCAGTGTG[A/G]AGGAGCAGAAGGCAT | 10477 |
rs377339078 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983502 | AATCAGGGAAAACAG[A/G]AATGGTTAAATTAGA | 10477 |
rs377339888 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036185 | GGTAAACATAGAGTA[A/G]TCAAAATAGTGTGGT | 10477 |
rs377372955 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998794 | CAAAGCAACAGATAC[A/G]TTTTTATCCAAAAAG | 10477 |
rs377466594 | in-del | -/AAT | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039691 | CGAAAAATTCATCTC[-/AAT]AATTTTATAATGACA | 10477 |
rs377485116 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048550 | AGGTCATTCTTGGGA[A/C]GAGGAGTAGGAAGAT | 10477 |
rs377521895 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985515 | TTTTTTACTATGTTA[A/C]TATGTTATTAGAATA | 10477 |
rs377533674 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013088 | CACCTCAGCTTCCCG[A/G]GTAGCTGGGACTACA | 10477 |
rs377547273 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061090 | TACTTTTAAAAGTAT[G/T]TAGGTGCACAGACCA | 10477 |
rs377598838 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979556 | TCCTTTGAGGCTCCA[C/T]CACCGGAACAAGTTC | 10477 |
rs377607430 | in-del | -/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990030 | AAAGTGATTTTTTTT[-/T]CCACATACCAATTTT | 10477 |
rs377621757 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979128 | GAGATATTCTATCTG[C/T]TCATTCTGAGTGGAA | 10477 |
rs377626723 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028280 | ATACGATTTTATTAC[A/G/T]TGGATATACTTGTAT | 10477 |
rs386653254 | in-del | AAC/G | | | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979694 | TGGTAGAACAAACAA[AAC/G]TGTCACTATCTCCAC | 10477 |
rs386653255 | multinucleotide-polymorphism | GA/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987269 | CCCTATTTGTATTTA[GA/TT]GAGAATTGTTGACTA | 10477 |
rs386653256 | multinucleotide-polymorphism | GGA/TGG | | | intron-variant, cds-indel, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990276 | GTAGGTAGACGTCAG[GGA/TGG]TACTGCTGAATACCC | 10477 |
rs386653257 | multinucleotide-polymorphism | AA/GT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001275 | AATGAGGTAAAATAT[AA/GT]CACTTAATCAGGAAA | 10477 |
rs386653258 | multinucleotide-polymorphism | CA/TG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002247 | ATAAGAGTACTAGTA[CA/TG]CAATTAACAATATAA | 10477 |
rs386653259 | in-del | CTAT/TATCTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025398 | TGTCATTGAAGATAT[CTAT/TATCTA]TTTTTTCCCTGACAG | 10477 |
rs386653260 | in-del | C/TATTGATGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029783 | ACTTGTCATCTTTAA[C/TATTGATGT]TTGGCGTGGGTGTTT | 10477 |
rs386653261 | in-del | CATGATAAAA/TATGATAAAAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039641 | AATGCTAATTTTGGC[CATGATAAAA/TATGATAAAAT]TTCTAATAGTGTCAC | 10477 |
rs397712432 | in-del | -/CT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053604 | ACCCCTTGTATCTCT[-/CT]GCCCCTGCACAGACA | 10477 |
rs397713718 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017661 | ATCCATTTTTTTTTT[-/TT]TAATACGGAAGTGTC | 10477 |
rs397750505 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052630 | ACTTTCACACATTTT[-/T]AACACCACTAACATT | 10477 |
rs397772070 | in-del | -/A | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022749 | AAAACAAAAAAAAAA[-/A]CCCCACAGGTTTACA | 10477 |
rs397870069 | in-del | -/T | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048664 | TCCTCTCACCCTAAT[-/T]GTCTGTATTATAGCT | 10477 |
rs397936953 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057389 | TGCTTGCAGGTTTAG[-/G]AGGGGTGTGTGTTTC | 10477 |
rs397937488 | in-del | -/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991826 | TTCAAGCCCAAGTGG[-/G]ATGGAGCAGGGCAAT | 10477 |
rs397943942 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000572 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 10477 |
rs397968175 | in-del | -/TTTAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010880 | GCCTCAGACTTTTAT[-/TTTAT]GCGTGCTTTGAGTAC | 10477 |
rs397986846 | in-del | -/A | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056099 | AAAAAAAAAAAAAAA[-/A]GATGCTAACATGTTG | 10477 |
rs398080864 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026743 | GCCTAAATACAACTT[-/T]TGTGTCAGTCAATAT | 10477 |
rs398080865 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061788 | ACCTTTTTTTTTTTT[-/T]TAAGTTGACTTACTT | 10477 |
rs398090904 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062594 | ATTCATTTTTTTTTT[-/T]ATGAAGGGGACTTTC | 10477 |
rs527244897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995870 | GTGATGTTAGCAGCC[A/G]TTGGAATACAGCTCT | 10477 |
rs527310045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003980 | ATAAATGATGGAAGC[A/C]AGATTCAGTTTTAGG | 10477 |
rs527342024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001266 | AGGAAATGAAATGAG[A/G]TAAAATATGTCACTT | 10477 |
rs527369538 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018651 | GAAGAGCTTGAAGGA[A/G]GTCATTTTAATTGAA | 10477 |
rs527376430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042798 | ATAAAGAAAATTACA[C/T]AATAGTAGGAGCTGT | 10477 |
rs527404841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006341 | AAGGCACACCTCCCT[G/T]TTCAATGTATATGCA | 10477 |
rs527407552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013478 | CAGTTCCTCACTGGC[A/T]GTTGGCAAATGGCCC | 10477 |
rs527439034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048837 | ATATTACAGAAGCTA[C/T]CTGTGTTCTCCGCCT | 10477 |
rs527442383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055459 | CCTTCCCATCTTGCC[A/G]TATGTTTTGACTAAC | 10477 |
rs527467863 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988454 | ATGCATAAGATTAAT[G/T]ATATTTAATTCAATA | 10477 |
rs527503704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054867 | TGGTGATATTTAAAG[C/G]TTAGGGTGATAAGGA | 10477 |
rs527591074 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010414 | GTGGGTGTACAAGTC[A/G]CGCTCTTATTGCAGC | 10477 |
rs527608502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981750 | TCTGTTTCATGCCTT[C/T]TGAGAAAGTAGACAA | 10477 |
rs527616948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061869 | CGGCAGAGATACATA[C/T]GCAATAGATAGTGAC | 10477 |
rs527630561 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034145 | GGATCTTGAACTAGA[A/G]ATACCATTTGACCCA | 10477 |
rs527639061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050320 | AAACTTGAATTTTAT[A/G]TCATTTTGTTTTTCC | 10477 |
rs527691463 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032146 | TTGAACAAATTTTAT[G/T]CCTAGCTTTTCTTGG | 10477 |
rs527708503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049882 | TTTAAACAAAAGACT[A/G]TGAAATACTACTACT | 10477 |
rs527721524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015129 | TGGAAGGGGTTCACA[A/G]CTTTTATATGCTTAT | 10477 |
rs527737438 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014209 | TAGTTTTTGTTTTCA[A/G/T]TGGTTGTGGTTGTGG | 10477 |
rs527781901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021220 | TTGCTGACAAATAAG[A/G]TATTAATCCTAATGG | 10477 |
rs527798023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020797 | TAAGGTAGTCATAAA[A/T]AATAGACAACTTGAA | 10477 |
rs527817756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056619 | ATGAGGGATCTACCC[C/T]TCTGACCCAGACACT | 10477 |
rs527832792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983732 | ATAAGCTTGAAAAGA[C/G]AATTTCTTTGGTAAA | 10477 |
rs527843772 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042944 | ATTTCCAAGCCTTTT[A/C/T]AATACAGTTTACTGC | 10477 |
rs527861761 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054334 | TATTTTGCATTTCCT[A/G]TACCATTTTGTATTC | 10477 |
rs527880786 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063731 | CGCTCACTCAGGAAT[A/C]TGGTAATGTCTTATG | 10477 |
rs527907553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027035 | TTGTGCAGAGAATTG[C/T]GCAGAGTATCTTAAC | 10477 |
rs527927033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990793 | ATTCAGTTTGACATT[A/G]AATTACACACAGGTT | 10477 |
rs527963526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996502 | CAAGAAGCATCCTCC[C/T]TTGTTTAGTGTTTCT | 10477 |
rs527967174 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990433 | TTGCTTTTGACTGTT[G/T]TCCTGTCTTATTAGT | 10477 |
rs527978373 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026530 | TTTTTTTTTTTTTTT[A/T]AATCCTTGATACATG | 10477 |
rs527982380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032292 | AATTGCATAAAATAA[C/T]GTGTATCCAACATTA | 10477 |
rs528090786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058320 | CTCATTTTGTACCTT[A/C]TGTGGGTATGATGTA | 10477 |
rs528188784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028641 | TTAATTTGCATTTCC[C/T]AATAATGAGGTTGAA | 10477 |
rs528235392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991311 | ATACTGTGTTTTTTC[C/T]TATACATACATACCT | 10477 |
rs528256819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038446 | GTTGTTAAACATTAA[A/G]TGACACATGACCATA | 10477 |
rs528262238 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033539 | TTAATTCAAGATGGA[G/T]TAAAGACTTAAATAT | 10477 |
rs528266478 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034654 | CACGTTGTGCACATG[C/T]ACCCTAGAACTTAAA | 10477 |
rs528336347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002819 | TATCTTCGATTATCT[G/T]TTGTTCCCTCTTACC | 10477 |
rs528366764 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997644 | TCAAAAGTACCTGCA[G/T]TTAGCTCTCTTAATT | 10477 |
rs528370099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044512 | GTGACAGATAGAATG[C/T]AGGTTTACTTTAATA | 10477 |
rs528449060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992838 | AACTAATTTTGTATT[G/T]TTTTTTTAGTAGAGA | 10477 |
rs528471346 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007624 | TGGTTGAACTTTGGT[C/T]TCCAGAGTTACCATC | 10477 |
rs528514451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999242 | GCAGTTCCTAGTACT[C/G]TGACGTTCCACAGTA | 10477 |
rs528527451 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026952 | AATTTGCATTTATAA[-/T]TTTTTATGTAGATTT | 10477 |
rs528564073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039726 | GACACTGATGTCTAG[A/G]AGTTAAATAAAATTT | 10477 |
rs528617641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039348 | ATACAATAAATGGCT[A/G]CATTGAAAATGTAAT | 10477 |
rs528638433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004034 | CTTCATCACACTGCC[C/T]GCATCAGGTGTGAAT | 10477 |
rs528638806 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010433 | TCTTATTGCAGCTGG[A/C]AGCATGTCAGTCTTA | 10477 |
rs528639024 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045753 | GTACCTCTTAAGAAG[A/G/T]TTGCTTATTAGAATA | 10477 |
rs528656724 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052358 | TCATCCTCTTTTTCT[C/G]TTATCACTAGAGACA | 10477 |
rs528681861 | in-del | -/TTTTTTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061110 | TGCACAGACCACTTC[-/TTTTTTTTTTTT]TTTTTTTTTTTTGAG | 10477 |
rs528688060 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998355 | GGGTGGCCTACTAAA[-/TG]TGCATTTTAAGAAGG | 10477 |
rs528701028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009737 | TTTCTTCTGACTCCC[A/G]TACTGTAAAGTACAA | 10477 |
rs528736124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016507 | TCTTATTTAATATGT[A/G]ACACCCTATGAGGCT | 10477 |
rs528739856 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041259 | AAAAAAAAAGATAGA[-/T]TTTTTTTTTTCTTCA | 10477 |
rs528799391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023357 | TAATCTTTCATAGTA[A/G]ATAGAACATCCTCTA | 10477 |
rs528820263 | snp | A/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063627 | ACCTTAAATAATCAA[A/T]AGTGGATTTTGACCC | 10477 |
rs528824327 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992927 | GAGTGGCTGCTCCAC[-/T]TTTACAAAACAGAAC | 10477 |
rs528832583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058894 | TTAAAGTGCTTTACC[A/G]TGTGGTCCCATCAGC | 10477 |
rs528850969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034177 | CAATCCCATTACTGG[A/G]TATATACCCAAAGGA | 10477 |
rs528853696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027948 | ATACTGATGATTTCT[C/T]ACCCAGCTTAAAAAC | 10477 |
rs528925349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991264 | TCAAGACTCCCTAGT[A/G]GATGCCTGAAAGTTG | 10477 |
rs528964981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033396 | CTACAACTATCTGAT[A/C]TTTGACAAACCTGAC | 10477 |
rs529022749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996722 | ATTGTAGTGATAGCA[A/G]ATCATAATGCTGTAA | 10477 |
rs529038092 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039622 | ACAAAAAAACAAGTG[C/T]ACAAATGCTAATTTT | 10477 |
rs529053893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181043912 | CGTAAGTGATTTAAC[C/T]GTTATTTCGTTGGAC | 10477 |
rs529057083 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004618 | AGTCTGGCGAAGAGC[A/G]AGACTCCATCTCAAA | 10477 |
rs529058111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037259 | CTGGTTTATGTATTT[A/T]CTGTACTTTTTATTG | 10477 |
rs529098702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002294 | TTTCATGTTTAATCT[A/G]TATTATTCATTAATG | 10477 |
rs529115804 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984612 | TCGTTTTCTACAGAA[C/T]GCATTGTTGGAATTA | 10477 |
rs529124055 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036300 | CAGCAGAAATGCCAA[G/T]GTAATTCAGTAGGGA | 10477 |
rs529166783 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996914 | GTTTTTACACCTCCC[C/T]GCAATTCTGAACCCT | 10477 |
rs529193248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014155 | TGCAGTGCCATATTC[A/G]GAGATAGGAAATCCT | 10477 |
rs529207193 | snp | A/T | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039284 | CAAAATGGTGAATAA[A/T]TTTTATAAATAAATT | 10477 |
rs529207424 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014763 | TTTGAGATACATGTG[-/AT]ATATGATACCTTTAT | 10477 |
rs529283921 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013839 | AGAAATAGACCATGC[C/T]TCTTCATGGAGGAAT | 10477 |
rs529345842 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009610 | CAGATAACCAAATAT[A/G]TTTCAGTATACACCA | 10477 |
rs529347129 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048053 | TTTTCCTATGCTTTG[A/T]AGTCCTCTTTCCCAG | 10477 |
rs529365820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016329 | AAGCGATCCTGCTTC[A/C]TTGGCCTCCCAAAGT | 10477 |
rs529379125 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046539 | GAAAATGAAAACAAG[A/G]TGATCTGTCACATAT | 10477 |
rs529399871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044767 | CTTACATTAATCACT[A/C]TGTTAAAAGTCTTAA | 10477 |
rs529419747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051742 | TAGAATATGTGTGCA[A/G]ATTCTTAGGACTATT | 10477 |
rs529458561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051032 | CTTCGTACTTTCTTC[C/T]CAGTCTCATTCCTTT | 10477 |
rs529465198 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006812 | AGTTAGAAACCCTTT[A/G]GATCCTCTGATACTT | 10477 |
rs529480455 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005441 | ATGGCATTAATTCCA[C/T]TGGAAGCATGTAGAC | 10477 |
rs529494661 | in-del | -/CAAGTCTTAACATA | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038717 | TGTATCCAGAACATG[-/CAAGTCTTAACATA]CAAGTCTTATATCTT | 10477 |
rs529529115 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030290 | TATGATAAATTGAAT[A/G]TGTATATTTTTCTTT | 10477 |
rs529531579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058214 | GCTTCCAGAAATAAG[A/G]GTTTAATAATGTGAA | 10477 |
rs529550572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021437 | TTCCTCCCTTCCTTC[C/T]TTTCTCCCTCCCTCC | 10477 |
rs529584676 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989605 | GCAGAAATACTCAGT[A/G]CTCTGTGTGACTGGA | 10477 |
rs529609328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985315 | ACATGTGGCTATTGG[C/T]CTCTTCAGTTGTGGC | 10477 |
rs529663068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060080 | ATTTTATTTTAATAT[C/T]TTAGCCTAACAAGAC | 10477 |
rs529676753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052663 | CTAGTCCTTTTTATT[G/T]TCTAGCAATAGCCCA | 10477 |
rs529685163 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979422 | GTTGGCTCACTCAGT[C/G]TTTTCTTCTTTCCCT | 10477 |
rs529687292 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991010 | CACAGTAATGTTTCT[C/T]GACATTACTGTTTCC | 10477 |
rs529747170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024210 | TTCATTTGTCTTCTT[A/C]CAAGATGAGCCTCTT | 10477 |
rs529752264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010546 | TGCCTATCCTCCTGA[A/G]TCTGTGTTCTCTAAT | 10477 |
rs529773452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059630 | CTAACTCTTTGAAAT[C/T]TGGTATTTATTTTAC | 10477 |
rs529804524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023871 | CCTCCACGTAAGTTC[A/G]TGCTAGATAAATGTT | 10477 |
rs529812861 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978817 | TTCTCCCCTAAGCTC[C/T]TTACCCCACTAAATC | 10477 |
rs529813413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017443 | AAGCATGATCCCTCC[C/T]GGATTAAGCCAACAC | 10477 |
rs529849942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987132 | GTATTGGAGGGCCAT[G/T]GGCCATAGTGTACTA | 10477 |
rs529869368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029860 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCTCTCTGT | 10477 |
rs529910155 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051998 | ATTTCTGAGTCACTG[A/C]GGTATTTCCATATAG | 10477 |
rs529931261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029328 | ATCAAATTCCTTGGA[A/G]AAGTATTCTTGTGGT | 10477 |
rs529956734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992727 | AGTGAAATGGCGCAA[C/T]GTCAGCTCACCGCAA | 10477 |
rs529991251 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054193 | GGACATAAGTTTTCA[G/T]TTCATTTGAGTAAAT | 10477 |
rs529995642 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013786 | CTGCTGCTTTTGTTG[G/T]AGGTAATCAGAAAGT | 10477 |
rs530013783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031448 | CTTACAATGTTTCAG[C/T]AGCATATATTTTTAC | 10477 |
rs530041565 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039343 | AAAAATACAATAAAT[-/G]GGCTACATTGAAAAT | 10477 |
rs530057340 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011801 | TTTAAAATGAATGAA[A/C]CATGTGTCCTCCTTT | 10477 |
rs530076292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025217 | TACTTTGCACAATTA[C/T]ACTTGAATTCCTAAT | 10477 |
rs530077240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988929 | AAGGTCCTGGAACCC[A/G]CTTTTTATAAAAATT | 10477 |
rs530112887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994142 | GACATTTTTCTCATC[A/T]TCCCAGGTGCTTACT | 10477 |
rs530131792 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993900 | ATGATTTATTCTTGC[C/T]TCATACTTGTTTCTT | 10477 |
rs530193885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030961 | GTTGTGTTTCACTAG[G/T]TTATACTATTACGTT | 10477 |
rs530197419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993553 | TTTTGTTACCTTTTT[A/T]TTTTATTTTCCTTCA | 10477 |
rs530199263 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985427 | ATACTGCATTGACTT[-/A]AAAAAAGTTCATTAA | 10477 |
rs530217448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000566 | ATAACCTTTTTTTTT[C/T]TTTTTTGAGACAGAG | 10477 |
rs530254232 | in-del | -/GTA | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004249 | CCAATGGTGCAGTGT[-/GTA]GTAGTTCTAGTTGTA | 10477 |
rs530278907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005420 | TGCTCTATCCCCAGG[A/T]TAGGAATGGCATTAA | 10477 |
rs530286426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041213 | AGATCATGCCACTAA[C/T]GACAGAGCAAGACTC | 10477 |
rs530310580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047569 | TGAAAACTATAAGCT[A/G]TTCTCGAAACCCTCC | 10477 |
rs530365937 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000125 | ATTTCTAGATGTATT[A/C]GATACATACATATTT | 10477 |
rs530369137 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000491 | CAGCACAGAGTAAGT[A/G]TAGTATAAATGGTAT | 10477 |
rs530428839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058936 | TGAAATTATTTTTGC[A/G]TATGGGGAAGATTAA | 10477 |
rs530436830 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058812 | TCTAACAAGGTAACG[A/T]GTGCCATCTAGTGGT | 10477 |
rs530441529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011082 | TGAGCACAGGGTCTT[A/G]ACTTTTTTTTTTTTA | 10477 |
rs530618488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023465 | AAAATTAATGCTTTC[A/G]CCTTTCATTTGATAA | 10477 |
rs530633021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029258 | CTAGTAGGACAAGTA[C/T]CTGTATTTTCATTAG | 10477 |
rs530650934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986153 | TCATCCCTGCTTTCC[C/T]TTGTCACAACCTGTG | 10477 |
rs530662995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991792 | CATATACAGTATGGA[C/T]AAACTGGACAAAAGT | 10477 |
rs530690617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992201 | CTATCAGTGTCTACT[C/T]GTTTTTAAGTTGTTC | 10477 |
rs530751716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045513 | CATTCTTTCTGCATA[G/T]CTGCTCTCCCCGTCT | 10477 |
rs530786366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035619 | CCCGTGGGTCACATG[C/T]GTCCCAGGACGTTTT | 10477 |
rs530820790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039203 | GGGGTGGTGGATATG[C/T]TCTATATCATGGTTG | 10477 |
rs530881248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000115 | ATTTAACCCAATTTC[C/T]AGATGTATTAGATAC | 10477 |
rs530979337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993447 | TTCCAGCTTGTCTGG[A/G]GAAAAATAAAGACAT | 10477 |
rs531051799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004581 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACCG | 10477 |
rs531053207 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011018 | GCTTTCACAGACTTA[C/T]CTAATATAAGCCCTT | 10477 |
rs531087219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039859 | CTATTTGCATATAAC[C/T]TATGTATATCTTCTG | 10477 |
rs531142795 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046234 | AGCCACAGATAAGCA[A/G]GAAATAGATTTATTG | 10477 |
rs531168621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041736 | TGATGTTGCACACTG[C/G]TCACAAAAACTGTGG | 10477 |
rs531207290 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050506 | TCCAAATTATATGAA[A/G]CATTTAAAAGTCTGT | 10477 |
rs531227235 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003329 | ATCACATTATAGACA[A/T]TCTTGCCATTAGCAG | 10477 |
rs531228374 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026755 | CTTTTGTGTCAGTCA[A/G]TATGGTTATACTTAT | 10477 |
rs531238423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037861 | TAGTCCCAGGTGCTT[A/G]GGAGGCTGAGGTGGG | 10477 |
rs531252259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017390 | TCTGAGGTTGGGATG[G/T]TAATTTTTGAGTTAG | 10477 |
rs531262783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052512 | AACCCAGCTGTTTAA[A/G]GTATATGCTCATTGC | 10477 |
rs531286775 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043537 | TGTATATGCAAATCT[C/T]CCAAAATCCAAAAAT | 10477 |
rs531301759 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986932 | AAATATTCTTTAATT[A/C]GTATATAGTTATGTC | 10477 |
rs531305064 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020545 | CTTAATAATAATGTA[A/T]TAAAACTAGAATTAT | 10477 |
rs531314758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001172 | GCTTAAGAATTTTTG[C/G]TTTTCTGTACTCCAG | 10477 |
rs531334215 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047758 | ACCCACAGCCCCTCC[G/T]GGCCTCCTCCAGACC | 10477 |
rs531335770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054775 | GTGGTATTGGGAGCC[A/G]TAAAACTGCATAAGA | 10477 |
rs531349175 | in-del | -/AAAA | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022740 | AAAAAAACAAAAAAC[-/AAAA]AAAAAACCCCACAGG | 10477 |
rs531393082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005739 | TTCTATTTAACAGAC[C/G]TACATTTTTAGCTTT | 10477 |
rs531436183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018737 | ATTTCATACAGTTGG[C/T]AACATCTTAACAAAT | 10477 |
rs531457266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012035 | ATAGCTCCGCTTTGC[C/T]CTACTGCAAGGTAGA | 10477 |
rs531499917 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025122 | GAAGTAAAAAATACC[A/C]AATAATTTATAGGGG | 10477 |
rs531524660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054171 | ATCTGCATGCAGAAT[C/T]TTGTGTGGACATAAG | 10477 |
rs531598546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056514 | GAGAAACCAAGGAAA[A/G]CCACTCTTTTTAACA | 10477 |
rs531601750 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063585 | ATTAAATGCATAGAG[G/T]TTTTTTCCTTTGTTA | 10477 |
rs531734057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982776 | CGTATATCACAGGTA[A/G]CTTTCCTGGTTAAAT | 10477 |
rs531737193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055571 | TAGCCTTCACTTGTC[C/T]TAAACTAGGTGTCTT | 10477 |
rs531765142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983634 | TTGCAGTAGCCTGTT[A/C]ATTTTTACCTCAGTA | 10477 |
rs531769544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990344 | TATCTGGGCCAAAAT[A/G]TCTAGTGCTGAAGTT | 10477 |
rs531785597 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032224 | AGGCTAAAGCGAACA[A/T]CATTATTTCAAAGGA | 10477 |
rs531825248 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006970 | TAATATTTCTAGCAA[G/T]ATACTGCATTGGAAA | 10477 |
rs531829671 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015805 | ACTAAAATGATTACA[-/T]GGTCCTTGTTCCATA | 10477 |
rs531831508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026870 | AACTTTGATTATTGA[C/T]CATATAATATTTTGT | 10477 |
rs531836866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020217 | GGACAGGGCCGTGCT[C/G]CCTCTGAAATCTGTA | 10477 |
rs531848881 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021981 | GTCACTTTTTTACTG[C/T]TAAGGGTAAAAACTG | 10477 |
rs531883480 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030378 | GAGTGCAGTGGCACG[A/G]TCTCATCTCAGAATG | 10477 |
rs531897336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036718 | GGAATAAGTGGGTAA[A/G]CAATACTCTAACTTG | 10477 |
rs531909924 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994734 | CAATTTGAAAGAAAC[C/T]TGCAGGTGAATGGTG | 10477 |
rs531942752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047695 | TGTCTCTGGTACCAT[A/G]TTAGTCTAGCCTATC | 10477 |
rs531987119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995743 | ATTCAGGCTGGATTT[C/T]TTTTTTTTTTTCTGA | 10477 |
rs532014018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031624 | GTTTTTCTCTTTCTG[C/T]GCCCCTCCTCCTTGC | 10477 |
rs532023674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995150 | ATTTCTCCTGGTTCT[C/T]GTGTGTATTTTACTG | 10477 |
rs532062202 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018604 | AATTTCTGTGTTTTT[G/T]TTTTTTTTTTTTCCA | 10477 |
rs532130272 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022630 | TTAGAAACACTAGAT[A/G]GCACTTTAGCATTAT | 10477 |
rs532182064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011884 | AGTTACTTAATTTCA[C/T]TTTAAGAATAGTGAT | 10477 |
rs532275841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029979 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCT | 10477 |
rs532278028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035174 | ATTTATATGCATTCT[A/G]TATAAGGGATAACCT | 10477 |
rs532280687 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993431 | TGTCATTCTGTTTAA[A/C]TTCCAGCTTGTCTGG | 10477 |
rs532345930 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034541 | GTGGGGTGGGGGGAG[C/G/T]GGGGAGAGATAGCAT | 10477 |
rs532367388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024312 | TTAAAACCAGATTAC[A/G]AAAAAGTAAGACTTC | 10477 |
rs532369024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982605 | ATGAAATTGACACTT[C/G]CAGAGATTAGCAGTG | 10477 |
rs532387299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987933 | ACAAGATTCCTGGTG[A/G]ATTGTATATATAAGT | 10477 |
rs532392242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062569 | TCTAACTTTTTATAT[A/G]TAGCTCAAAATTCAT | 10477 |
rs532405391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981881 | TTGTACGTACCCCTG[C/T]TGTACGATGAAATAA | 10477 |
rs532493695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989624 | TGTGTGACTGGAAAC[A/G]TTTTCCAAAAGAGTG | 10477 |
rs532539472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054987 | AGGAGGATGTGATTG[A/G]CTGTGTCAAATGTTG | 10477 |
rs532540278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061951 | ATGCCCATTAATAGA[C/T]GTAACGTTTAAAAAG | 10477 |
rs532639853 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998041 | AAATGCCGTAGCACT[A/G]ACTATGAGAATAATT | 10477 |
rs532652896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031510 | ACATTACTCTGTGTG[C/T]TTTTATTTATTTAGT | 10477 |
rs532703677 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026047 | CTCATTTGCAGGGTC[A/C]ACAGAGCAGTTAATA | 10477 |
rs532789018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994387 | CTTCATCTATGCCTC[C/T]GTCCATTTCACCCTC | 10477 |
rs532804034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039019 | TTTTGGGGTTTCTTA[C/G]TATAAACATACACTT | 10477 |
rs532836040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996586 | ATTGAACATCCTCAG[A/G]CTCTGCTGACTAAAT | 10477 |
rs532969051 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979544 | GAATCCACAAATTCC[G/T]TTGAGGCTCCATCAC | 10477 |
rs533031117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995939 | GTCATACATGGTAAA[A/G]GTAAGATATGTGCTT | 10477 |
rs533034078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013610 | ACATTTCCATGTAAC[C/T]TGGACTTCTATAAAC | 10477 |
rs533110297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043267 | CATGTGAATAAATAT[A/T]AGAAAATGAATGCTT | 10477 |
rs533122061 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999091 | AATCCCTAAACATAA[C/T]ACCAGTACTGCTAAA | 10477 |
rs533122550 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980215 | CGGGAGCCACGACGG[C/T]CCCCGCGCAGGCGGA | 10477 |
rs533167837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051020 | TAGTTGAAGTTTCTT[C/T]GTACTTTCTTCCCAG | 10477 |
rs533264294 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022418 | GGGGAAATAAAAGAT[A/T]ATCTTTTTTTGATCT | 10477 |
rs533275599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013099 | CCCGAGTAGCTGGGA[C/T]TACAGTCATGCACCA | 10477 |
rs533278478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050402 | CTGCTGTTTTGTTCA[A/G]CGGGATTCTCTTCAG | 10477 |
rs533282332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015272 | ATATTTTAAGCCTAC[A/G]TATAGTCACATTAGG | 10477 |
rs533375635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021328 | TTATCCAGATAACCT[C/T]ACCATTACAGTGTTT | 10477 |
rs533407666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008825 | GTTTAATTTCTTTAG[A/C]GCTAAGCTTGAAATA | 10477 |
rs533419359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008096 | ATCAGTTTAAAGTTG[A/G]GCCTGGGTGATAAAA | 10477 |
rs533420917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015801 | AATCACTAAAATGAT[C/T]ACATGGTCCTTGTTC | 10477 |
rs533436781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027862 | TAAGTATACCCTTAT[C/T]ATCAATCATGTACTG | 10477 |
rs533441997 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043763 | TTGTTTACACAATAT[G/T]ATTACTGGTGTGTAT | 10477 |
rs533449092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027126 | TTCTTAGATTGTCTG[C/T]ACCTGTGTTAAAATG | 10477 |
rs533457137 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041077 | GCATGATGAAACCCA[A/G]TCTCTACCAAAAATA | 10477 |
rs533494874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058071 | TGCACATCAATAAAG[C/T]AGATAAATTTTATGC | 10477 |
rs533580899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045524 | CATATCTGCTCTCCC[C/T]GTCTCCAGTTGTTTT | 10477 |
rs533668096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020896 | TGGATTAAGTTTTAT[A/G]TTAAGTTTTTAGAGT | 10477 |
rs533703114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041409 | TAATTGTTAAAATGG[A/T]TGTCAGGGTTTTCTG | 10477 |
rs533732420 | snp | C/G | 0.00012451 | 0.00788919 | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989882 | ATGTTTACTTTTCAG[C/G]AAAATCAGCAAGTCT | 10477 |
rs533750222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025507 | CAGGTATATTTGGGA[C/T]ATATGGCATTTAAGG | 10477 |
rs533769066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047899 | GACAAGTCTCCTTCA[C/T]GTAGTCTTACAAGGT | 10477 |
rs533771907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995218 | ATGGTGTTAGTGGCA[C/G]TAGTGATGCTGGAAA | 10477 |
rs533850610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011346 | GGGTGATAAGGAGGT[A/T]GGGAGAGATAACTGC | 10477 |
rs533973503 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006357 | TTCAATGTATATGCA[G/T]TCTGTTCATATTGTT | 10477 |
rs534006708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040975 | TGCTTCAGGGCCGAG[C/T]GCAGTGGCTGACGCC | 10477 |
rs534030731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000409 | TATTACTGGTTGAAT[C/T]TAAAATGTTAACACT | 10477 |
rs534031469 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026776 | TTATACTTATACTTA[A/T]TTTACACATGCTAAT | 10477 |
rs534043686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005204 | TGCTTGCTTTCCTTC[C/T]TCTTAGTTGACTCCA | 10477 |
rs534068234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049320 | TTCACCACACCCACA[A/G]TTTATCCTGGCATCC | 10477 |
rs534072404 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983219 | GATTCATAAATACTC[-/AT]ATTTTTCTATGGATT | 10477 |
rs534073095 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005939 | TCTGGCAATTTCTTA[A/G]AAGAGGCTGTAGCCC | 10477 |
rs534135526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037013 | CATCATCCATAGTTA[C/T]GCATTGTATAATGAC | 10477 |
rs534136046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062721 | AGCATTTCATTTTAA[C/T]AGAATATTAGAACTA | 10477 |
rs534137834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055215 | GGAAAGATGATTGAG[A/G]TGGAAACTCGAAGGG | 10477 |
rs534138456 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028885 | TAAATTTATCAGTCT[C/T]TTATATGATTAGCAC | 10477 |
rs534419330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013238 | TACTTAACAAATTAC[C/G]CCACAATTTAGTGGC | 10477 |
rs534426107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021141 | TACCAGTCTTCGTGG[A/G]CTTTCACATATAGTA | 10477 |
rs534631278 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027738 | AAAATCAAGTATTGA[A/G]ACTGAATATAGTTCA | 10477 |
rs534662689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029462 | ATTTCTTTAATTCTG[A/G]TTTTGCTTTGTAATT | 10477 |
rs534708551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021849 | AGGTTGGAAAATACT[C/T]CTGGGTTTTGCTTTC | 10477 |
rs534720601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028126 | CGGCATATATTGTTT[A/G]ATTTTGAGCACTATA | 10477 |
rs534771407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028982 | CAAAGGCTTGCCCTT[A/G]GTGTTCCAAATTTAT | 10477 |
rs534828798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034375 | AGTTCATGTCCTTTG[C/T]AGGGACATGGATGAA | 10477 |
rs534841633 | in-del | -/AG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058016 | TAATTTGTAATAAAC[-/AG]AAAGAGTTTAATTCT | 10477 |
rs534891946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033132 | TAGATTCAATGCCAT[A/C]CCCATCAAGGTACCA | 10477 |
rs534920697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038316 | TGGGAGCAATAGGCT[A/T]TACCATATAACCTAA | 10477 |
rs534937587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009022 | ATATTATAGCAGTGC[A/T]AAGGATACTTATTCT | 10477 |
rs534953006 | in-del | -/AA | 0.278399 | 0.248382 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039282 | TTCAAAATGGTGAAT[-/AA]ATTTTATAAATAAAT | 10477 |
rs534954691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032642 | TTCTAAGAAAAATTT[A/C]CCATCTCTTTGAAAC | 10477 |
rs534956686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037291 | TATTTTAGAGTGTAC[C/T]CCTTATTTTTTTAAA | 10477 |
rs534958974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003119 | CCTGAACATCACTTT[C/T]GTGACAGGAAGTATA | 10477 |
rs534978950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986552 | TGACAAGTGCGTAAA[C/T]GAGAATTTTAGCTTT | 10477 |
rs534998794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008267 | AATATTTATTGACCA[A/G]TTACTATGTGGCAGG | 10477 |
rs535044810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044264 | GTTCAATAAGTACTG[A/T]AAAAGTGAATAGTGC | 10477 |
rs535068431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992438 | GTTGTGTTGTGATTA[A/C]AAACAAACCTAGAAG | 10477 |
rs535101268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056936 | GAGAAGGACACATAC[C/T]ATTTCAGCCAGACAC | 10477 |
rs535126597 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037297 | AGAGTGTACTCCTTA[G/T]TTTTTTAAAGTTAAC | 10477 |
rs535131549 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025034 | TTTTTAGAATTCACT[-/A]ATAAGCCTTTCATGT | 10477 |
rs535163804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020414 | CACTAATTACATCTG[C/T]AGTGACTCTGTTTCC | 10477 |
rs535171764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038752 | TTATATCTTAATAGA[C/G]AAACCAATTTAAAAT | 10477 |
rs535180725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983058 | TCTTATCAGTGGTAG[C/T]AGTAGTGGAATATCC | 10477 |
rs535242322 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026687 | TGTATGAGATTTGTT[C/T]CGCCATTACTTCAGG | 10477 |
rs535290691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062447 | ACCATTTTTGAACTA[C/T]TCATAAGCAGAAATA | 10477 |
rs535445416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985146 | ATAAGGTGATTTGAT[C/T]CTGATTTATCCGATG | 10477 |
rs535474322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984129 | TTTTGGTTTCAAATT[G/T]TGGAAAAATACCAAG | 10477 |
rs535475850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038694 | AAACCTCTGTCTGAT[A/G]AAAGACTTGTATCCA | 10477 |
rs535488388 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011084 | GCACAGGGTCTTGAC[-/T]TTTTTTTTTTTTAAT | 10477 |
rs535513024 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063262 | AATTATGTCATTTGT[A/G]TTAAACCCAGATCTA | 10477 |
rs535584042 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032979 | ACTTACAAGGGATAT[C/G]AAGGACCTCTTCAAG | 10477 |
rs535597228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038279 | TATTCTATATAATAA[C/T]ATACTGTGTGAGTTT | 10477 |
rs535665975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036930 | TTTCACATAAAGTTG[C/T]AGTTTCCAAGAACCT | 10477 |
rs535672536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043669 | AATATAATAATTAAC[A/G]ATAATCACCATAGAC | 10477 |
rs535704981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002564 | GTAATTTTCAGTTTT[C/G]TAGTAGCCACATTAG | 10477 |
rs535717619 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042037 | GTCAAAACTAAGAAA[A/T]TAATATTGGTAACTT | 10477 |
rs535762971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006985 | GATACTGCATTGGAA[A/G]TGTTAGGAAACAAAT | 10477 |
rs535780451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004384 | TCGCACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 10477 |
rs535800096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034320 | AAGAAAATGTGGCAC[A/C]TATACACCATGGAAT | 10477 |
rs535815144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991860 | AGATTTCATCGTGCT[A/G]CTTAGAATGAGGTAC | 10477 |
rs535852820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991390 | CAACTTCCCATTGGC[A/G]TATCCAAACTGCCAG | 10477 |
rs535859075 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044057 | CTTAATCAAATGACT[C/T]TTGATACATGTGGCT | 10477 |
rs535898773 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998100 | AAACTTGCCAGACTC[A/C]AAGTGTAGAGCACAA | 10477 |
rs535911717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997551 | TATCCCTTCTCATCT[A/C]CCCTAGGCTCTCATG | 10477 |
rs535934164 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996169 | GAGGGTAAAAGTCAT[A/G]TGGACCTATTTGGTG | 10477 |
rs535975923 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009263 | GGACACATTATAAAA[C/G]AAATAACTGAAAATC | 10477 |
rs535999157 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026214 | AATAATGATTGAAGC[C/T]AATACTTTAGATATT | 10477 |
rs536013620 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023699 | TGAGAGCATGGACTC[-/T]TATCTTGGTACCATC | 10477 |
rs536044615 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030822 | GGAATTAGAGCATTT[-/A]TTTTTTTCATGTCTG | 10477 |
rs536053986 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040937 | TTCTGATGCTTCAGC[A/G]CATTTCCTTTTCTCC | 10477 |
rs536066564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050447 | AGTTTGGGAGGGACT[C/T]TTAGAGTAGACACTT | 10477 |
rs536082885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008197 | GTTATTTTGCTTATG[A/T]TGTTTTGTTTCTTCT | 10477 |
rs536191980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007429 | ATCATTTTATAAATA[C/T]AAGAGAGTAGACTGG | 10477 |
rs536265300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045907 | CAACAATCAATTTGT[G/T]AAGTACTATTTTTCC | 10477 |
rs536269876 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991354 | CATAAGGGTTACAAA[A/T]TAGGCACAGCAAGAG | 10477 |
rs536275029 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018340 | ACCTGTGTTTACACA[A/T]GTGTTTAATATTTTT | 10477 |
rs536343633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010084 | CCCATTCTTGATTGC[A/C]GGAATGTTTTACTAA | 10477 |
rs536349882 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993387 | CCAAAGTTTTTTTGC[A/T]GCTTTAGTGTTCCAG | 10477 |
rs536351344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030459 | TATATTATCTTTTTT[A/C]AATATGAACAGTCTT | 10477 |
rs536378246 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047457 | TATCTTTTGGATATC[C/T]CATAAACTTCTTAGT | 10477 |
rs536526499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985855 | CGTGCATAAATCTAG[A/T]GAGCCTAGTAGACAT | 10477 |
rs536530536 | snp | G/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990478 | ATATTCACCTACACC[G/T]TCCTCAGCTGATTCT | 10477 |
rs536574727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055673 | TTTACTATCCTGCAA[C/T]AGTTAAATGTACACT | 10477 |
rs536657532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060388 | TGGATGTGTATGCAA[A/G]CAGACGTACCCACAC | 10477 |
rs536744086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008516 | GTGCATTTCTAGTTC[A/T]GGCTGAGGTCCAACT | 10477 |
rs536755653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024006 | GTTTTATATTTCTTT[C/T]GCATTTGTAACCTCT | 10477 |
rs536826399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057569 | TGGGGCTTATTTCTT[C/T]TATACTTATTTTACT | 10477 |
rs536847549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053547 | TTTTTAAATTAATAG[C/T]TTTTTCTGGGCAGTT | 10477 |
rs536985554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034653 | GCACGTTGTGCACAT[A/G]TACCCTAGAACTTAA | 10477 |
rs536987618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039970 | TCTTATTAGTTTTTT[C/T]CTGCATATTTTCTGT | 10477 |
rs537022040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023979 | AAGTGATAAAGCAAT[A/G]GGAATACCTGTGTTT | 10477 |
rs537046512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003359 | GTACTCATGTTTCAG[A/G]TGACCTCTAATGAGC | 10477 |
rs537049030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051150 | TCATAAACAATATGT[A/G]GGATCTTTTTTATGT | 10477 |
rs537055353 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012896 | CCCTACTATGTGTTA[C/G]ACATTGCTTGGTATT | 10477 |
rs537092952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059311 | AATAAATATTTAATA[G/T]AAATCTGCTCATGAA | 10477 |
rs537126506 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996000 | TTTTCAAAATAATGA[G/T]TTGGTGTCCTAGTAT | 10477 |
rs537131348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992974 | ACCTACCACATTTAT[A/G]TATTTCATTTTAAAT | 10477 |
rs537137383 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030041 | GTTTCATCATGTTGG[A/C]CAGGATTTTCTTGAT | 10477 |
rs537146428 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016024 | TTGTTCAATTCAACT[A/G]GCTTTATAAAGTTAT | 10477 |
rs537153172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022750 | AAAACAAAAAAAAAA[A/C]CCCACAGGTTTACAG | 10477 |
rs537154871 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998833 | CAAAAAAATCGTCAA[C/T]GGCAGTTCCTTCAGA | 10477 |
rs537198182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029525 | AATTTATTTCTAGGA[G/T]TTTAATATTTTTGAT | 10477 |
rs537215588 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028701 | ATTTCTGTGAAATGC[C/G]TTTTTTTTGTTATTT | 10477 |
rs537259410 | in-del | -/TTCT | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021509 | TTTCCTTTCCTTTCC[-/TTCT]TTCTTTTATTCTTTC | 10477 |
rs537268014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034444 | AGAAAACCAAACACC[A/G]CAGGTTCTCACTCAT | 10477 |
rs537328178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028209 | TTTTTCTCTTAAATC[G/T]TGTTTTAAGATTTAT | 10477 |
rs537378319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038794 | TTGAATAGAGATGTT[A/G]CTGATGAAGCTGTAT | 10477 |
rs537393474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027434 | CTAAATAAATTTGAA[A/G]TAGGAACTATTTGAC | 10477 |
rs537400906 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978918 | ACGTACAGCTTTCCT[C/T]TTCTGTCTCCCCATT | 10477 |
rs537403086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033776 | AAATTTTTGCAAGCT[A/G]CCCATCTGACAAAGG | 10477 |
rs537432741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059820 | ATTCTTTTCAGGAAG[A/G]CACTTTTGAGAGCAT | 10477 |
rs537648434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053516 | AATATTTGCTTGTTC[A/T]AAAATTTATTTGTAT | 10477 |
rs537654367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046434 | TAGAGTCTGTGTTTA[A/G]TTTAAGCCTCATGAT | 10477 |
rs537679190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011250 | AAAATCCAATATCAG[C/G]GTGCTGGCAGGACCT | 10477 |
rs537743301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018288 | TGCATTCTGGTGATG[A/T]ACCTGTATACATAAA | 10477 |
rs537755630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017592 | ATCCTTTTGGGAAAT[A/G]TAGCTTTTTCTAGAC | 10477 |
rs537770492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045790 | GAGATTTTCTCCACA[C/T]TGTTCCCTCCCTTCC | 10477 |
rs537809598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994555 | TCCGTAATCAGTCAT[C/T]GTTTAGGTTTACAAA | 10477 |
rs537845413 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993719 | ATCATTTTCTCACAT[G/T]AAATTCTAGTAGGTC | 10477 |
rs537870338 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982665 | ATGATCATATTTGCT[A/G]GAAAATTTGCAAATT | 10477 |
rs537884335 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000756 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10477 |
rs537898154 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048711 | TCCTAATTGCTTTCA[A/G]CCTAAATAAATATGA | 10477 |
rs537898430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000266 | GATTATTAAGTGACA[C/T]TGGGATACATGAATA | 10477 |
rs538096927 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980455 | CGGACGCGTGCACCC[C/T]CAGGGTGAGGGGAGG | 10477 |
rs538116373 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026266 | GTTGTTTAGTATAGC[A/T]AATATAGATTACATA | 10477 |
rs538119484 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992225 | GTTGTTCTTTGTTTA[C/T]TGGGTTGTTTTTCCA | 10477 |
rs538138402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010611 | TAAAAGGAAAATAGT[A/G]GATAGCAGAATTTTT | 10477 |
rs538150292 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019408 | TAATCTTTTTTCTAC[C/G]TGTAATATAAACTTT | 10477 |
rs538207009 | in-del | -/AGATA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998962 | TCTCTATAGATATGC[-/AGATA]AGATGTTTTAAATGT | 10477 |
rs538221065 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032283 | CCTGGTAGCAATTGC[A/G]TAAAATAACGTGTAT | 10477 |
rs538230975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049163 | CTGCTGGACAGAGCA[A/G]CTTTTTGAGTGTAGG | 10477 |
rs538233777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000187 | AGAATAAGACTCACT[C/G]TATTATAAAACAAAC | 10477 |
rs538240063 | in-del | -/GCC | 0.00478085 | 0.0486577 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981201 | CCGCGGAGCTGCGTG[-/GCC]GCCGCCGCCGCCGGC | 10477 |
rs538254638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003818 | TGATTTCAAATGCAT[C/T]ACTTGTTCAGTGTGG | 10477 |
rs538276418 | in-del | -/AAAAC | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062300 | TTCAGAATTCTACTT[-/AAAAC]AAAATGGCAAGTAAG | 10477 |
rs538322616 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007668 | TGTGTCAATGTATTC[C/T]TTCTGCCAAGACTGT | 10477 |
rs538328406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988243 | CTCTCACTGTTGCTG[G/T]CATTTTCTCTAGTGC | 10477 |
rs538348098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012323 | TTATGCAGTTGACAG[A/G]GTATTGGTTAGTTAC | 10477 |
rs538348763 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019630 | TACCAGTGATTTTTT[A/T]AAAAAGTCTACTTAC | 10477 |
rs538371786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046364 | TTCCATACCTGCCCT[C/T]GTATATCAAACTGCA | 10477 |
rs538391668 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985938 | TACTTTACATGTTTA[A/C]CTCCGGAATGTTTCC | 10477 |
rs538391672 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005716 | ACGGTTATATAGTTA[C/T]ATATTTTTTCTATTT | 10477 |
rs538416087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025980 | GTAAAAATATTTTAA[C/T]GTCATTCAAAACATA | 10477 |
rs538416100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018974 | TCTAGCTCTAAATTT[A/T]TTTTTTGAGATGGAG | 10477 |
rs538429255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054440 | CCATTCTAATAGGTG[C/T]GTAGTGGCATGCTTT | 10477 |
rs538435127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052796 | AGGGTAGACTCCTTG[C/T]TTTATTTTCTTTGTT | 10477 |
rs538447219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052101 | AGCCATATTATTAAT[C/G]TGAGTGAATCTTATC | 10477 |
rs538458355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059756 | GGGCATACTCTCCTC[C/T]TCCCCCACTAAACTA | 10477 |
rs538486865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017562 | ACCTCATGGAAATGC[A/G]GTAATATGCATACCA | 10477 |
rs538521250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025454 | GCTTTGTTAGGTAAG[A/G]GAACTTTGATACTTC | 10477 |
rs538532433 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992812 | GACTGTAGGCATGTG[C/T]CACCACACTCAACTA | 10477 |
rs538668303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999616 | GTTTTTTTTCATTAT[A/G]GGCACCCTCCCGCCC | 10477 |
rs538685125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012229 | TGATTAGTTTCAGTA[A/G]ATGTACATGTATAAC | 10477 |
rs538691649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004713 | CTTGTCAGTTTATGT[A/G]TATGTCCTTTGCACA | 10477 |
rs538722012 | snp | A/T | 0.416871 | 0.186156 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061112 | CACAGACCACTTCTT[A/T]TTTTTTTTTTTTTTT | 10477 |
rs538748507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018865 | TCATAAACAATTACC[C/T]GAGTTGGATGTCAGG | 10477 |
rs538755384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004423 | GCAGATCACGAGGTC[A/C]AGAGATCGGGACCAT | 10477 |
rs538772646 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980336 | GCGGCCCCGCGATAC[C/G]GTGCCCGCGCCCCCG | 10477 |
rs538779885 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052647 | ACACCACTAACATTG[A/G]CTAGTCCTTTTTATT | 10477 |
rs538865996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010219 | ATTAATTGTGGTTCT[C/G]TATAGTTCTTTTTCA | 10477 |
rs538893878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988339 | GCAATTTGTTTTTTA[A/T]TGTCAGTAAAAGCAG | 10477 |
rs538916092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016763 | TTCATATATTTTACT[C/T]AAATATATTTCAGAA | 10477 |
rs538925957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023563 | AGTGTGAGGCATCCC[G/T]TACTTTCTTTAACAC | 10477 |
rs538935217 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052293 | GGGAAAGAATACAGT[C/T]GTAGGTTCTTGAAGT | 10477 |
rs538971221 | in-del | -/CTGCAAGG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012038 | CTCCGCTTTGCTCTA[-/CTGCAAGG]CTGCAAGGTAGAGTG | 10477 |
rs539002284 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035743 | GTATTTTATATGTGA[C/T]CCAAGACAATTCTTT | 10477 |
rs539002324 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035316 | GGGTTGCAGTAGTAC[A/T]GTCAGCTGCTGATTT | 10477 |
rs539019584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026659 | ATTTAAATATTTGAC[G/T]CCGGCCCTTTCGTGT | 10477 |
rs539037619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054366 | CCACTAGCAATGGAT[C/G]AGAGTTCCTGTTACT | 10477 |
rs539039056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063047 | CCCCAAAAAGGTAAA[C/T]GCTATCAAGAGTAGA | 10477 |
rs539132207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032394 | CTTTTATATACATGG[A/G]TTACAAAAAAGTCAT | 10477 |
rs539137606 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025365 | AATGTAATTTTCACA[C/G]TGTCATAACATTGAT | 10477 |
rs539195705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031870 | AGTTTAATTTTAATC[A/G]GCTCCTTTCCTGATT | 10477 |
rs539220581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036453 | TTCCTGGCAGGGGCC[A/G]TTGTGTGGAGTTTGC | 10477 |
rs539228263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995357 | AAGCTTACAATATTG[A/G]TAAATACAGTATAGT | 10477 |
rs539279257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041876 | GTGTGAGTCAAAACA[C/T]CTCATCCTTGCCATC | 10477 |
rs539301352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006426 | TTCCAGATTCCATGA[A/G]GGATACTACTTCTGG | 10477 |
rs539316827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030547 | TTTTTTTCTTACACC[C/T]AATTAGCCTGTTTTT | 10477 |
rs539364492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005933 | ACTGCTTCTGGCAAT[A/T]TCTTAGAAGAGGCTG | 10477 |
rs539390264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019854 | TTTTTTTGTGGTGAG[A/G]ACATTTAAGATCTAC | 10477 |
rs539452970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996347 | TAGGAGAACTGAGAG[A/G]TCTTTATTATAACTA | 10477 |
rs539472440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037386 | GGAGATGACAGCTCT[A/G]TGTGTATGTTATTGC | 10477 |
rs539573310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043622 | CTGAATTATTGTATA[A/G]TATTTGATAAGACAA | 10477 |
rs539586865 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022165 | TATGGCAAACATACT[A/G]TAAGTTTAGGAGTCA | 10477 |
rs539597402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982967 | AAACATATTTAATTG[A/G]ATGTAAGTGAAAGAT | 10477 |
rs539599529 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003477 | TCCAGGGGGGATGAC[A/G]CTGTCTCAAGATTTA | 10477 |
rs539617382 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028135 | TTGTTTAATTTTGAG[-/C]ACTATACATTACATA | 10477 |
rs539644501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035933 | TTTGGTGTTGAACTC[C/T]ATAGGTATAAAGTAA | 10477 |
rs539673570 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044309 | TACAACTAAAAATTT[A/G]GAAACTGACTATATG | 10477 |
rs539694502 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024265 | TGACACTTTATGTGA[A/G]AGTAAAACTTAAAGT | 10477 |
rs539757471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041507 | TTGTAGTGGCACAAC[C/T]GGCTCACTGCAACCT | 10477 |
rs539827759 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053993 | ACTAATATGCATTTA[A/C]GTTTCATCCATATCT | 10477 |
rs539848409 | snp | A/G | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063821 | TAACTGTGATGTGGT[A/G]GCTAGTCTGTGATGC | 10477 |
rs539849147 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979900 | GGACATTTTAAACAC[C/T]GTTTTGGATTTTTAA | 10477 |
rs539885167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002911 | AACCTTTCTTGGCTA[C/G]AGATAACTAGATGTG | 10477 |
rs539888565 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060532 | TTAATTTTGTTATTA[A/T]ACCTAATCTAAGTTT | 10477 |
rs539897307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002464 | AGGAATGATTACGAA[C/T]GAAGAAAACCCTCTA | 10477 |
rs539957412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002063 | CAGTATCATAGAAGC[C/T]TAGTTGGCATTAGCT | 10477 |
rs539969088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042781 | CTGGGTTGGAAGTAG[G/T]GATAAAGAAAATTAC | 10477 |
rs540009535 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005296 | CTTCAGATTGAGATG[C/G]AGTGTGAAATAGCGT | 10477 |
rs540014373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036164 | CTACTTGATTCTGAC[A/G]TACTAGGTAAACATA | 10477 |
rs540036333 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011768 | ATCATACCATTATTT[C/G]TTGTTTTTATTTTGG | 10477 |
rs540053949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014349 | CAACTCAGAGAAGCA[A/G]CCTGGGTTGGAAATT | 10477 |
rs540073608 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008792 | CAAGCAAATGTTAAA[C/T]AGTTATTGAGAGTGA | 10477 |
rs540198346 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018519 | ATGAGCTTTTGTGCC[C/G]GAGGACTCAGGGGAG | 10477 |
rs540199171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004000 | TCAGTTTTAGGTCTG[A/T]CTGACTGAAGGTCAT | 10477 |
rs540212919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995123 | GTAAATTGTGTATTG[C/T]GGTAAAAAGTGATTT | 10477 |
rs540289486 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025106 | TTGGAAGTATTCTCA[A/G]GAAGTAAAAAATACC | 10477 |
rs540313808 | snp | C/T | 5.02508e-05 | 0.00501227 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181062846 | CAACAGAGCAGAACA[C/T]GACAGGATAGCCAGA | 10477 |
rs540319566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988547 | TTTCCCCTTTTAAAA[C/T]AGAAGAATTTGTGAT | 10477 |
rs540440565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993300 | TTATGGTTATTCACA[A/G]CAAATGAAGCTTTGA | 10477 |
rs540534722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999246 | TTCCTAGTACTCTGA[C/T]GTTCCACAGTAGGCT | 10477 |
rs540576498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984228 | GTGCATTAAACAAAA[A/G]TTGTAGAAGGTGAAC | 10477 |
rs540582848 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032089 | ATAATCACTTTGCTG[A/C]GGTTTTCATTCCCTG | 10477 |
rs540633657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995555 | TTCCTTTTTTTCTAA[C/T]CTATAAGGTTCTCAG | 10477 |
rs540645342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031452 | CAATGTTTCAGTAGC[A/G]TATATTTTTACCGTT | 10477 |
rs540651873 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007857 | AATAAGAAACTGAAT[G/T]TATAATTCAATTTTA | 10477 |
rs540669120 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037194 | CAAACTTGTGCTGCC[A/C]GCAAATATAATTATA | 10477 |
rs540674726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001468 | ATGTAGAGGGTGGGA[C/T]ATCAAGAAGTGGAAA | 10477 |
rs540732044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014028 | TGTAAGAAGTAGATA[A/C]TACAAAAGGTGTGCC | 10477 |
rs540795495 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013509 | TAGTTTCTTGACTTG[C/T]TGGCCTACCTGTAGG | 10477 |
rs540811418 | in-del | -/ACAC | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990798 | GTTTGACATTGAATT[-/ACAC]ACAGGTTAGAAATGT | 10477 |
rs540887563 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054071 | GTTGTCTGGAGGTAC[C/T]ACAGTTTATATATCC | 10477 |
rs540896298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047629 | AAGTCTGGTTGATTT[G/T]TGTTTTGTTTTGTTT | 10477 |
rs540921444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062502 | TGAATGAAAGGCCAA[A/C]ATTACAAAATAGTTT | 10477 |
rs540952219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982494 | ATTAGACTAACATTC[C/T]GACAGATTGTTTAAG | 10477 |
rs541092083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049607 | TAAGATAGACAAAGC[A/G]CAAGCTTTATAGTAA | 10477 |
rs541167544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028384 | GATTACTGAACATGT[G/T]TTCTAGTAATATGTG | 10477 |
rs541177717 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033916 | ATGCAGCCAAAAGAC[A/G]CATGAAAAAATGCTC | 10477 |
rs541179610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027807 | ACTCTACTTTCCTAG[C/T]CATTTGATTGTACAG | 10477 |
rs541188723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020520 | CACAGTTGATTAAAA[A/G]ATTTTGATCCTTAAT | 10477 |
rs541206396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021265 | TTGTGAAGTCATATA[G/T]TCATTTAAGTTACAT | 10477 |
rs541239964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033339 | AAACGGAGATATAGA[C/T]CAATGGAACAGAACA | 10477 |
rs541255343 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000397 | AATAGGCATATATAT[C/T]ACTGGTTGAATCTAA | 10477 |
rs541260838 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063438 | GCATAGTTTCCTGTC[A/G]TAATATTTTAAGTCA | 10477 |
rs541382653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015695 | TCACTAGGAAAAATC[A/G]ACATTTAAAAAATAA | 10477 |
rs541395115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996538 | GGGGCATCTTGGTTA[C/T]TTTTGACTGGATTGT | 10477 |
rs541416604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042777 | GTATCTGGGTTGGAA[G/T]TAGTGATAAAGAAAA | 10477 |
rs541470769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048752 | AACACTCAGGAATAA[C/T]AACTGTTCACTTATA | 10477 |
rs541492714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022356 | TGGTGTTATGTTCCA[A/T]AAAGTTGTCAAACAC | 10477 |
rs541524611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985221 | ACATGAATGTAAACT[A/C]ATTTTAAGGAGATGG | 10477 |
rs541572040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019919 | TGTTAACTGTAGACA[C/T]GTTGCTGTACATTAG | 10477 |
rs541584309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019254 | TGTGAACCGCCGCAC[A/C]CGGCCTAGCTCTAAA | 10477 |
rs541612304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991468 | TGTTTGAAAATAAGC[A/G]CTGCAGTAGTCTATA | 10477 |
rs541612408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984651 | TTAAGCAAATGTCCT[A/C]ATTGCTTGGGAACAT | 10477 |
rs541621660 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016398 | ACCTTTTTGTCTTTA[C/T]CAATAAAAATGACAG | 10477 |
rs541654836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991197 | TCTAGAATTGTAGAT[A/G]AGCAGTTATGGCCCT | 10477 |
rs541661324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981506 | TAAATTTCCAAGTGT[C/T]GTGTTTAAAGGCTTT | 10477 |
rs541708431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997304 | TTCATATTTTTGTTA[A/T]CTGGCTTTTCCTCTT | 10477 |
rs541729809 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999322 | AAGCATTTGGTATAG[-/T]TTTATCTCCTCACCA | 10477 |
rs541735276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037585 | GACAAATACAAAGGA[A/C]AATATTTTTGTACAG | 10477 |
rs541748266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989449 | TTTATTAAATATCCT[A/G]TACATTCTTTACCTT | 10477 |
rs541755260 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996888 | AAAAAATTTCTTCCT[C/T]TAGCCCTTTAGTTTT | 10477 |
rs541799685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031418 | CCTTGAGGCTATTTT[A/G]TTATGTAGAGCAAGC | 10477 |
rs541808152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057185 | ATTTTTTAAAAGGGT[A/G]TTACCGAATCAGTTG | 10477 |
rs541940639 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983161 | TTATTGATAACTAAA[G/T]GAAAAAGAATATAAA | 10477 |
rs541946418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983643 | CCTGTTAATTTTTAC[C/T]TCAGTAAAAGTCACT | 10477 |
rs541973902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037504 | TGTGTATGTTTGTGT[C/T]TTAGTTTTTACAAAA | 10477 |
rs541976261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982354 | TACTTCATTATCAGT[G/T]TAATTGTACTTGAAT | 10477 |
rs541999720 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026953 | ATTTGCATTTATAAT[A/T]TTTTATGTAGATTTT | 10477 |
rs542011806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032749 | TTCAGAACCACTGCA[A/G]TTTTTGGGCAAGCGC | 10477 |
rs542028000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062399 | ATTTGAAATAGCATG[A/G]TATTGTAAGACTGGG | 10477 |
rs542034979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037133 | AGTCATCGTAGCATC[A/G]TCAGACAGTGCATTA | 10477 |
rs542177263 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040520 | ATTGAGCAACTCTTA[C/T]GTGGAAAGCATTATA | 10477 |
rs542207385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984431 | CTAAGCTTTAAAGTT[A/G]CTGCTTGTGTGTGCA | 10477 |
rs542257760 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045180 | TTACTTGTGCTGTGT[A/G]TGAGTAAGAAGGTTG | 10477 |
rs542353188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033278 | TACCTGACTTCAAAC[A/T]ATACTACAAGGCTAC | 10477 |
rs542456499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996436 | CTTTATCAGAATCAA[A/G]TTAATTTGTCACAAT | 10477 |
rs542546497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007991 | AGCATCCACTGAAAT[C/T]AAAGCCAAACAAATA | 10477 |
rs542551942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001658 | AAGGATTCTTACATG[C/T]AAAGGCCATAGGAAA | 10477 |
rs542639402 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027986 | TATCATTGAATCTCT[A/G]TATGTTGTCTGTCCC | 10477 |
rs542639644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010665 | TTTTTCTACATTTGT[A/G]TAAACAGTGTTTTCT | 10477 |
rs542702881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010316 | ATACTATTTCTTGTC[A/G]GTCATATTCTGTATT | 10477 |
rs542715013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017173 | TGGGGAGAAGGTTAA[A/C]GCCTGAAGGAAGGAC | 10477 |
rs542761862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036396 | ATAATGGTTCATTCA[A/G]CATTGTATTGTACTT | 10477 |
rs542772088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038411 | ATCCCCGAATGACAC[A/G]TTTCTGAGGTCATAT | 10477 |
rs542776581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016381 | CACCATGCTTGGCTA[A/G]TACCTTTTTGTCTTT | 10477 |
rs542803708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044439 | TCAGGGCAAACCCAG[A/G]TCATAAGGGATAGAA | 10477 |
rs542825019 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059694 | TTTAAGAGCTGTATA[C/T]GCACATGTAACTAGT | 10477 |
rs542834210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008548 | GATATATACAGCAGT[C/T]CTGACTGGGTAAGGG | 10477 |
rs542864133 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054353 | CATTTTGTATTCTCC[A/T]CTAGCAATGGATGAG | 10477 |
rs542933339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015608 | TGATAAAGGTAAGAT[A/G]ATTTTTTACTTTAAA | 10477 |
rs542945807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015074 | AAAACGAAGTACAGA[A/G]TTGTTTTTTTCTTAA | 10477 |
rs543032743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004516 | TATGCACCTGTAGTC[A/T]CAGCTACTCGGGAGG | 10477 |
rs543059640 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992066 | ATTTTCATTTGCTTT[C/G]CTTTCTTTTTTACCT | 10477 |
rs543079713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052279 | GCAGGGGTGTCCAGG[G/T]GAAAGAATACAGTCG | 10477 |
rs543154832 | in-del | -/T | 0.376791 | 0.215463 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029660 | TATCTGTAGACAATC[-/T]TTTTTTTTTTTTTTT | 10477 |
rs543183482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007375 | TACTTAGCCCTACAT[G/T]TTGCTCCCTATTGAT | 10477 |
rs543222406 | in-del | -/A | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063660 | TGGTCTCAAACACAT[-/A]AAGTTGTACTTCGGT | 10477 |
rs543241028 | snp | A/C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031335 | TCAAAAACAAGATAC[A/C/G]TAGAAATGTGTTTGC | 10477 |
rs543279147 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991028 | CATTACTGTTTCCAC[A/C]CCAAAAATGTATTAA | 10477 |
rs543285635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023161 | CCATCCTAACATCTG[A/G]AAATCATTAAGTAGA | 10477 |
rs543293804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986039 | CTCTTTATATACCAG[A/T]TTTCATTTAAGTCCT | 10477 |
rs543312858 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035084 | AAACTATTCGGATCA[C/T]TTAGGTGCTTTATGG | 10477 |
rs543335370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014128 | GCCCATGTTTCTGAC[A/G]TAAGTATTAAATGCA | 10477 |
rs543348873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029165 | GGGCTCTTCCATTCT[A/G]TTCATCAAGTTGTCT | 10477 |
rs543379279 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033242 | TCCTAAGCCAAAAGA[A/G]CAAAGCTGGAGGCAT | 10477 |
rs543379623 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008177 | GGTATGCCAATCAGG[C/T]ATATGTTATTTTGCT | 10477 |
rs543404583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038019 | ATTTATTATTGTGGA[A/C]GAAAAGTATTTTTGT | 10477 |
rs543409819 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013932 | GTTTGCTACAGAAGG[A/G]AGAGCAAGAGCAGAT | 10477 |
rs543421476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016944 | TAAGTTAGAAGCCAG[A/C]GCCTGGAAATGCCAT | 10477 |
rs543446895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044389 | TTGTATTATCTATGG[C/T]ACTATGTATGGCAAG | 10477 |
rs543511086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043831 | CATGAATATTTCTCC[A/G]TGTCATTAAACAGTC | 10477 |
rs543544696 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016608 | GTAGAATCCCAGCTC[A/C]AGTCTGTTGACCCCC | 10477 |
rs543567079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029069 | ATGGATAACTATTTG[G/T]TTTAGTAACTTTATT | 10477 |
rs543573451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014879 | CTCTTCGAGCTACTT[G/T]GAAATATATAATAAA | 10477 |
rs543600894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015808 | AAAATGATTACATGG[C/T]CCTTGTTCCATATAC | 10477 |
rs543621500 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999056 | CTACCTCAAACTTGT[G/T]TTGAGGCAAATGTAG | 10477 |
rs543623153 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050225 | TTCAAGCAAGAGTTA[C/T]ATACTAGTATAGATT | 10477 |
rs543627866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028476 | ATTCAACCATGCAAG[A/T]TAATGCCAAATTGGT | 10477 |
rs543638870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058106 | GAGGGAGAAGATCCT[A/G]TGAACCTTCATTAAT | 10477 |
rs543654514 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025729 | TACATATATTAGCAG[C/T]GAAGAATCATTTCAG | 10477 |
rs543660961 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058385 | CTGAGTTCATTTGAA[A/G]TATGAATTAGATGGA | 10477 |
rs543684492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049683 | ATTATTGCATTATCT[G/T]TGCAGATAGAAGCCT | 10477 |
rs543726652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021173 | TGTAGTTGCGACTAC[A/G]AAACATGAGATTAGT | 10477 |
rs543752542 | in-del | -/TGAC | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040107 | TTTTAAGTGGCCATT[-/TGAC]TGTTTCCTTGACATT | 10477 |
rs543762835 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020844 | CTGGATTTCCCTGAC[A/G]TGGGTAAATCTAGTG | 10477 |
rs543773564 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979314 | ACTGAATGACTGTGT[A/C]TTTGGAAAATTATGG | 10477 |
rs543796516 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036138 | GAAAGAACGAAGTTG[G/T]AGGACTCATACTACT | 10477 |
rs543855676 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060320 | AACATTTCTTTTCTT[C/G/T]CTCACTTTCTGTCTT | 10477 |
rs543861838 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061761 | ATTTCACACATTTTG[-/T]TTCGTTATGTGACCT | 10477 |
rs543886646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030227 | AAATTTTAATGAATA[C/T]TTTATCTACTAAAGT | 10477 |
rs543925900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010279 | GTGTGTCAGCTAGTT[A/G]CAGGGTTAATATGTT | 10477 |
rs543996351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040358 | TAAATTCAATTAGAT[A/G]TCATTTATTTCTTTT | 10477 |
rs544001167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985281 | AGAGCTATGCTGTCC[A/G]GTAATGTAGCCACTT | 10477 |
rs544002192 | in-del | -/CTTC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021664 | TTCCTTCCTTCCTTC[-/CTTC]TTTCCTTCCTTCCCA | 10477 |
rs544008803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035059 | CATAATAAATATACA[A/C]GTCATTTGTAAACTA | 10477 |
rs544035552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059656 | TTTACACTTCTAGTT[C/T]GTCTCAATTCACCTT | 10477 |
rs544128742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034091 | GTGGGACTGTAAACT[A/G]GTTCAACCATTGTGG | 10477 |
rs544185942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010251 | TCAGATAAATCAGTA[A/G]GCTTAATTTCAGGTG | 10477 |
rs544200200 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007919 | ACATTTAATGAAGTC[C/T]TGAACCCTTATCAAG | 10477 |
rs544214900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994118 | CAGTGTCCTTGTAAA[A/G]TTTTAAAAGACATTT | 10477 |
rs544219603 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024700 | TAGTGACTACTTATA[C/T]GCTCATCATCTAGAT | 10477 |
rs544246266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023862 | AACTGGTGCCCTCCA[C/T]GTAAGTTCGTGCTAG | 10477 |
rs544389674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005308 | ATGCAGTGTGAAATA[C/G]CGTGAATCTTGGCCC | 10477 |
rs544453707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011627 | ATGGTATAGAAGTGC[C/T]ATTTTAACTGTTAGT | 10477 |
rs544455929 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997371 | CTGTTAGTATTTTTT[C/T]ATATGACTTATTCTG | 10477 |
rs544475466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060501 | AAAAAATTTTTTTCA[A/G]CTGAGTCAAAAGCAT | 10477 |
rs544491619 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002971 | TACAAAAATGCAGGC[A/T]TCTTTTCAAGGGTTT | 10477 |
rs544513835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004453 | TCCTGGCCAGCATGG[C/T]GAAACCCCGTCTCTA | 10477 |
rs544556657 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001054 | AGAATATGACACACT[A/G]ACTCTTAAAGAGGCA | 10477 |
rs544573022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035978 | AAGTGATGTCAGTAC[A/G]GTGCATTCTTCAAAC | 10477 |
rs544575693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986962 | CTAGTACATACATAC[C/T]CAGGGTGATCTTAAG | 10477 |
rs544630209 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983606 | AAATATTGTCAGAAC[-/T]GTTAATGTGCTCTTG | 10477 |
rs544636389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041564 | CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGATTAC | 10477 |
rs544680009 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988965 | TTAATTGGAAGCTCG[A/T]CTGTAAAACAGATAA | 10477 |
rs544680675 | in-del | -/TTCTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029730 | AAGTCATAATTGAGC[-/TTCTT]TTCTTGTTCCATGTT | 10477 |
rs544717577 | in-del | -/TGTT | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058190 | GATAAAAAGTAAAAC[-/TGTT]TGACAGCTTCCAGAA | 10477 |
rs544741365 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006436 | CATGAAGGATACTAC[A/T]TCTGGATCTAGGATG | 10477 |
rs544748706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041172 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGGCTG | 10477 |
rs544814251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039583 | TGAGACCATCCTGAG[A/C]AACATGGCGAGACTC | 10477 |
rs544827916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046870 | TGCTTCAGCCATAGC[C/G]CCAGTTTTGACTTAT | 10477 |
rs544847671 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010376 | TTATTTTTTTGAGGT[C/T]GTCACTTTAGCTGGT | 10477 |
rs544907047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018488 | TCTACCTTTCAGTGC[A/T]GTTAATCTATTCTTG | 10477 |
rs544966195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024776 | TTTTATAAATGAAAA[A/T]CTACACACTAAAAAC | 10477 |
rs545034656 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001486 | CAAGAAGTGGAAATA[-/C]AACAAAAGAGACAAT | 10477 |
rs545043994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029238 | ATTCTAATGAGTCTT[C/G]ATATCTAGTAGGACA | 10477 |
rs545083918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992165 | TTGTATGCTTAAGAG[G/T]TCTTTTCTCTTAAGG | 10477 |
rs545103589 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010833 | TTTTTTTTACATTTT[C/G]CATGGATGTGTTTAT | 10477 |
rs545167160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010435 | TTATTGCAGCTGGCA[A/G]CATGTCAGTCTTATA | 10477 |
rs545190730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045380 | TTAATGAGTTTTGGC[A/G]AAAGTTATAATAGCT | 10477 |
rs545200369 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013087 | CCACCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC | 10477 |
rs545263283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035730 | CATTAATGTTAGTGT[A/G]TTTTATATGTGACCC | 10477 |
rs545274096 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010576 | TGTAAGAAAGATGAT[C/T]TGAGTTTCACAGGTA | 10477 |
rs545315196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003377 | ACCTCTAATGAGCAA[A/G]TATGGTATTCTCACT | 10477 |
rs545315635 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059917 | AATTTTTTTTTTTCT[C/T]GGCAACTCCAATTAT | 10477 |
rs545325435 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008708 | TGGACTAGTTAAAGG[C/G]AACGTCAGTGGGAAT | 10477 |
rs545373771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048151 | TTCCTCTGACTCTTC[C/T]CTTATCTCTCTAACA | 10477 |
rs545383337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035176 | TTATATGCATTCTAT[A/G]TAAGGGATAACCTTT | 10477 |
rs545395058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040622 | ATTTAGTATAAGGTA[C/T]ACTACAAATTATAGG | 10477 |
rs545421161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047484 | TAGTCCCAGTGTATC[C/G]AAAACCAACTTTTTT | 10477 |
rs545482962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046775 | GTTTGATAAGAAAGC[A/G]TATCATAGAAATTAC | 10477 |
rs545541546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025568 | TAATAGTTGTAAAAT[A/G]CCACATATTAATTTT | 10477 |
rs545555738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025025 | TTAATAAAGGTTTTT[A/G]GAATTCACTATAAGC | 10477 |
rs545576496 | in-del | -/TTC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021342 | TCACCATTACAGTGT[-/TTC]TTCTTTTCTCTTCTT | 10477 |
rs545619012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030816 | TTTCTAGGAATTAGA[A/G]CATTTATTTTTTTCA | 10477 |
rs545658600 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052364 | TCTTTTTCTCTTATC[A/G/T]CTAGAGACAGAAACT | 10477 |
rs545667310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017269 | TCAAGACTCCTGGAA[A/G]TAGATGTGTGCAGGT | 10477 |
rs545730802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023791 | GACGATGATAAAATA[A/T]CTACCTGATAATTTT | 10477 |
rs545747519 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017294 | GCAGGTAAAGGCTGA[A/G]GTCCAGGAGGGGCCA | 10477 |
rs545763221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055233 | GAAACTCGAAGGGAG[A/C]GAGAAATAGAGATTT | 10477 |
rs545774164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994015 | TTTGAAGGCTTTGAA[C/T]GCAAACTCAGAGACA | 10477 |
rs545808931 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036332 | AGGATTTCGACATAA[A/G]GTGTTAGAATAACTG | 10477 |
rs545866478 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056798 | AAATATTGCTTATTG[C/G]TTGCAGGGAAAAGAT | 10477 |
rs545896915 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980870 | TTTTCCCTCCCCCCC[C/G]TTCCCCCCCCCACAG | 10477 |
rs545900140 | snp | A/G | 0.000101027 | 0.00710657 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060827 | GGTAAGCAAATCTTT[A/G]TTAACATGTACAATA | 10477 |
rs545958041 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000647 | GCAAGCTCTGTCTCC[C/T]GGGTTCACGCCATTC | 10477 |
rs545991422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989328 | TGTATCTTTTCCTTA[C/T]TTCACATGGTGCTTT | 10477 |
rs545991429 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980000 | AGAGGTTGTTCCCCT[A/C]ATCTCCAAATACATT | 10477 |
rs546001645 | in-del | -/T | 0.327211 | 0.237778 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029840 | AATTAATTCGGTCCC[-/T]TTTTTTTTTTTTTTT | 10477 |
rs546006790 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990186 | CCAGCCACCAGGCTA[A/G]GCGACAATTGGTAAT | 10477 |
rs546009612 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058636 | ACTATGGTGAAATGT[G/T]TTTCTTTTCCAACAT | 10477 |
rs546012915 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995695 | CTTAGTGTTTCTTGT[A/T]TGTTTGGGAGTTAGA | 10477 |
rs546041252 | snp | C/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063252 | GATGGCTAGGAATTA[C/T]GTCATTTGTATTAAA | 10477 |
rs546088710 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037841 | GGCATGGTGGCATAT[A/G]CCTGTAGTCCCAGGT | 10477 |
rs546182138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026807 | GGCAATATTAGATCT[A/G]TTGAACAGATATCAT | 10477 |
rs546228572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053365 | AACCACCTTAGTTCT[A/G]TGGTCCAAATGTGTT | 10477 |
rs546239246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052729 | GTTTCTAATCATATC[A/G]AGACCTAGTTTTTAA | 10477 |
rs546314106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037063 | CTCATATATAATGGT[A/G]GTTCCAGAAGATTAT | 10477 |
rs546407650 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023078 | TGCATTCAGTAGAAA[C/T]CATAACCCCGACATG | 10477 |
rs546447238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041679 | CTGACCTTATGATCC[A/G]CCTGCCTCAGCCTCC | 10477 |
rs546450489 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978827 | AGCTCCTTACCCCAC[C/T]AAATCCTATCAGCAA | 10477 |
rs546451982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001535 | GATACAGCACCAGAT[A/G]AGTAGGTTTGCTTAA | 10477 |
rs546469157 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060594 | ATATATTACCCTTCA[-/T]TTTTTTTTTAGTGTT | 10477 |
rs546525925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006188 | ATTCGTATCACCAGG[A/G]TAAAATAAACAGTGA | 10477 |
rs546540084 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006241 | GTACAGAAAAAATTC[C/T]CCAGTCAAGATTCCC | 10477 |
rs546554826 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030905 | TTGACCCAAAAATTT[A/T]AAAAAAATTTTAGTT | 10477 |
rs546586984 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011093 | TCTTGACTTTTTTTT[C/T]TTTAATTAGTTAGAG | 10477 |
rs546612807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046314 | TGAACAAAAATGTAG[C/T]ACAAAACACAAATAC | 10477 |
rs546687931 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980309 | CCAGGCCGGAAGCCA[C/T]CCCGCGGCACAGCGG | 10477 |
rs546693707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025279 | CACAGAAACCTTGCT[C/T]TTAACATTTAAGACA | 10477 |
rs546699476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018043 | AATTTTGTTTTCGTT[G/T]TATTTTTAACCTAGC | 10477 |
rs546723709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994235 | GCACGTTGCAATTAT[C/G]ACTTTTCCCTTCTGC | 10477 |
rs546726878 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002897 | GTGAAAAGATGGACA[A/G]CCTTTCTTGGCTAGA | 10477 |
rs546770040 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031285 | TTATTATGTGGTTCA[-/T]GATATTCTGTATCTT | 10477 |
rs546787424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023544 | AAGACAGAGGAATTC[A/G]GCCAGTGTGAGGCAT | 10477 |
rs546823414 | snp | A/G | | | upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980290 | CCTCGCCCCGGAGGC[A/G]GGCCCAGGCCGGAAG | 10477 |
rs546915563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992755 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 10477 |
rs546924486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025706 | TAATAATCTTCTACA[A/G]TCACATCTACATATA | 10477 |
rs546948609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981837 | CGGCAAATCCCTTAA[C/T]GCTGGCGTTGTGTGA | 10477 |
rs546952152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992374 | ATGTATTTTGCCTTG[C/T]ATTATTTAAGTGCAA | 10477 |
rs546953281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040887 | TTAGAAAAGCAGAAG[A/T]CTTGAATTTTCATAA | 10477 |
rs546967965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000127 | TTCTAGATGTATTAG[A/T]TACATACATATTTAT | 10477 |
rs546986676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032315 | CAACATTAATTTTTA[A/G]TCGGTAATATTTTTT | 10477 |
rs547058198 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040843 | ATCCAGAGAGTTAGA[A/C]TGTGCAGTAAATGAG | 10477 |
rs547171405 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048592 | AACCACTAGCACATA[C/T]CTAGGTCTGCCCTTT | 10477 |
rs547172449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041293 | AGAGTGTCAAATAGC[A/G]CTTGAACCAAAGCCC | 10477 |
rs547213950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030472 | TTCAATATGAACAGT[C/T]TTGGATATGATTTGT | 10477 |
rs547226448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035264 | GCATGATGTAAGGCT[A/G]TAAATGTATATTCCT | 10477 |
rs547247174 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032172 | CTTGGGTTTAGAGGG[C/G]AAAATTAACTTTTTT | 10477 |
rs547322900 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026117 | AATCTGTTGGGATAA[G/T]GAATACTTAAATAGT | 10477 |
rs547438218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057217 | CAACATTATAATACA[A/G]ATTGTACTTTAAAGA | 10477 |
rs547442026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002446 | TTTTTTGAAGACAAA[C/T]TTAGGAATGATTACG | 10477 |
rs547460923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001793 | CGGAGAGAAAGAGAA[C/T]AAGCTGGATGCAGTT | 10477 |
rs547515354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043608 | GAGGGATACTTAACC[C/T]GAATTATTGTATAAT | 10477 |
rs547546004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048852 | CCTGTGTTCTCCGCC[A/T]ACTTCACACATGCCC | 10477 |
rs547694824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020278 | TTGTGTTTTTGACGT[C/T]ACTCTACCTCCATTG | 10477 |
rs547719912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032842 | CAGCAAAGTCTCAGG[A/T]TACAAAATCAATGTG | 10477 |
rs547727476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061931 | GAGTATTGGAAACAA[C/T]CTCAATGCCCATTAA | 10477 |
rs547747092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044115 | CTCCGATCTAGTGGT[A/G]TTTGAGCATAACTGT | 10477 |
rs547765727 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062940 | GCATCTTCTCACTGT[C/G]CTGCAAATCTTTATA | 10477 |
rs547774652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036325 | TAGGGAAAGGATTTC[A/G]ACATAAAGTGTTAGA | 10477 |
rs547779583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008081 | AAGTATTGAGATTTA[A/G]TCAGTTTAAAGTTGG | 10477 |
rs547811091 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026533 | TTTTTTTTTTTTAAA[A/T]CCTTGATACATGCTT | 10477 |
rs547846644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041365 | TAGAACATACTACTT[G/T]TTATATAGATGTCAG | 10477 |
rs547895038 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007649 | ACCATCCTGGAAGGG[A/G]CAGTGTGTCAATGTA | 10477 |
rs547900985 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010934 | GATTTCTTTACTAGT[G/T]AGTGTCTTGAATTAA | 10477 |
rs547957828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014325 | AGTTGGCTACATTTC[A/C]TTCTGATACAACTCA | 10477 |
rs547992692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027036 | TGTGCAGAGAATTGC[A/G]CAGAGTATCTTAACT | 10477 |
rs548000833 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063744 | ATCTGGTAATGTCTT[A/G]TGGAACATGTTGCTT | 10477 |
rs548058219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018741 | CATACAGTTGGTAAC[A/G]TCTTAACAAATGACC | 10477 |
rs548104871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990833 | TGCTCTTCATTTGGG[A/T]TTTATTTTCATCATT | 10477 |
rs548112866 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020075 | TGTATTTCTTATCTG[-/T]TTTTTGTGGGAAGGT | 10477 |
rs548119873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025140 | TAATTTATAGGGGCA[C/T]GAGTGGTTTGAAGTA | 10477 |
rs548132738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054236 | GATTACTGGATCTTA[C/T]GGTAAGATATGTTTA | 10477 |
rs548238719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048278 | TTGGCTGAAATCTCC[A/G]TTGTATATTTAGTTT | 10477 |
rs548264152 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036578 | TTGTCCCCACCTGAG[A/T]GAGTGAGGGGGTGTG | 10477 |
rs548295555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000766 | TCACCGTGTTAGCCA[C/G]GATGGTCTCGATCTC | 10477 |
rs548299153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062645 | TACATATGATCATGT[C/T]ACTTTAAACTTTTTC | 10477 |
rs548349250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054794 | AACTGCATAAGATAA[C/T]CAAAACAGTATATGT | 10477 |
rs548359570 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039538 | CACTTTGGGATTTCG[A/T]GGTGGGCAGATTGCT | 10477 |
rs548399617 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018088 | CTGCTACAGTGATTG[C/T]GCTTTGGCTTCACTT | 10477 |
rs548400612 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988975 | GCTCGACTGTAAAAC[-/AG]ATAAATACAGAACTA | 10477 |
rs548405889 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055993 | TCTTGGTTTTTCTTA[A/C]AACATTCGCACTGAA | 10477 |
rs548442812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011262 | CAGGGTGCTGGCAGG[A/T]CCTTCTTTCTAGGAT | 10477 |
rs548453363 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980163 | GCGGGGGACTCCCAA[A/C]CACGCGCCCAGGGCC | 10477 |
rs548477635 | snp | C/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063680 | TGTACTTCGGTAATA[C/T]GATGTTTAAGCCAAA | 10477 |
rs548491022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988806 | ACATGTAGATAGACT[C/G]CTTTTTCTTCTTTAC | 10477 |
rs548493720 | in-del | -/TC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021356 | TTTCTTCTTTTCTCT[-/TC]TTTTTTTTTTGTTTT | 10477 |
rs548499676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036728 | GGTAAACAATACTCT[A/G]ACTTGTTTTTTATTA | 10477 |
rs548520381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021736 | GGTCATGGAACCATA[A/T]AAAGTAATTTAGCAG | 10477 |
rs548568506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014161 | GCCATATTCGGAGAT[A/G]GGAAATCCTGGAGGG | 10477 |
rs548631066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031701 | GTTTTGTTTTGTTTT[A/G]CTCATAATTCCATTC | 10477 |
rs548633641 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056083 | GGAAGGAAATGCTTA[-/A]AAAAAAAAAAAAAAA | 10477 |
rs548677081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013687 | GGAAGAAGAGAGGGA[A/G]CTCATGGGTGTGTAT | 10477 |
rs548678898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020758 | GTTAAAGTGGGTTTC[A/G]TATGTAATGCATAAG | 10477 |
rs548690324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982794 | TTCCTGGTTAAATTA[C/T]GATTATCCCTTCCTG | 10477 |
rs548706083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990905 | TCCTTTATTTGAAAC[A/C]CTTGGGGCCAGATGT | 10477 |
rs548739174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020218 | GACAGGGCCGTGCTC[C/T]CTCTGAAATCTGTAG | 10477 |
rs548751392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019645 | TAAAAAGTCTACTTA[C/T]TATTAGTTTTTTTAA | 10477 |
rs548775799 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984727 | ATGAATTGGAATTGT[A/G]GGAATTCATTTTAGT | 10477 |
rs548783097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032226 | GCTAAAGCGAACATC[A/G]TTATTTCAAAGGAAA | 10477 |
rs548840910 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003271 | TTTTTATATTAACAG[C/T]GTTTAAGCAAACATG | 10477 |
rs548852086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995746 | CAGGCTGGATTTTTT[C/T]TTTTTTTTCTGACAG | 10477 |
rs548896043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033067 | ATTCCATGCTCATGG[A/G]TAGGAAGAATCAATA | 10477 |
rs548937503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995177 | ACTGTGTTTCGTGCA[A/G]TACTGTAAATAACAC | 10477 |
rs548966655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039293 | GAATAAATTTTATAA[A/G]TAAATTTATACTTCA | 10477 |
rs548973536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984894 | TACAAAATTGAACAC[A/G]CATAGAAAACAATAT | 10477 |
rs548994865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004171 | ACTTTCTCTGTATTA[C/T]ACAGAGTTTGAAATT | 10477 |
rs549056119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019466 | TCATTTTTAACTTGG[C/T]GGTTGTTTCATCTTG | 10477 |
rs549066721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009624 | TATTTCAGTATACAC[A/C]AAAATAAACACTTCA | 10477 |
rs549093805 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046264 | GAATTTTGAGTCTTT[C/T]GCAGGTCAGGGATTC | 10477 |
rs549099784 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043245 | CTATTTTTTTACTAA[A/G]TACTTACATGTGAAT | 10477 |
rs549136685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998721 | CATCAAATTGTGGTG[C/T]AAACAGCTGAAAGTA | 10477 |
rs549183742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045702 | CCAAGGTTGGGACCC[A/G]TGGTTTCAGATGTAG | 10477 |
rs549201248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037262 | GTTTATGTATTTACT[A/G]TACTTTTTATTGTTA | 10477 |
rs549213082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044104 | CTGTATTTCTCCTCC[A/G]ATCTAGTGGTATTTG | 10477 |
rs549240862 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050404 | GCTGTTTTGTTCAAC[A/G]GGATTCTCTTCAGAA | 10477 |
rs549272663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043359 | ACATGAGTGGCTGAG[A/G]TACAGTGCTTTCTGA | 10477 |
rs549298420 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051770 | ATTAAAATACTTAGT[A/C/T]CAACCTAATGGAGTA | 10477 |
rs549310026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015330 | TAGCTTATATGTGTT[C/G]TTTGTGAACTAAATT | 10477 |
rs549332838 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993070 | AGTTAAATTGTAAAG[-/C]CTTGGGATTTTTATC | 10477 |
rs549395266 | in-del | -/GATAAGGAGAGTGGGATAAGGAGAGTGGGATAAGGA | 0.00998776 | 0.069958 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998461 | GATAAGGAGAGTGGG[lengthTooLong]GAAGGGGCAGGGGGA | 10477 |
rs549447254 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989674 | CTTCCCACTAAACTT[A/C]ACATTTTTATTAAGG | 10477 |
rs549455211 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022575 | GAAGCTCATCTAAAC[A/C/G]TGTATTTTATCAGTA | 10477 |
rs549458385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003630 | CACTGAATTTGAATA[G/T]TATAAAACTTTATAA | 10477 |
rs549470559 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994168 | TTACTATCCACATTT[A/C]CATTAGAAGATGCCA | 10477 |
rs549521365 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027867 | ATACCCTTATCATCA[A/G]TCATGTACTGCATAA | 10477 |
rs549536433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001926 | TTAAGTATTTGTTGA[C/T]GAAAAGAAATGTGTT | 10477 |
rs549541978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044881 | TAATGTCAGTGGTGC[A/G]CTGGTTAATGTTCTA | 10477 |
rs549565593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990474 | TAATATATTCACCTA[C/G]ACCTTCCTCAGCTGA | 10477 |
rs549581922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032436 | ATTCAAATGGCCCCT[A/G]TTTAACGAACCTCTG | 10477 |
rs549628673 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011887 | TACTTAATTTCACTT[C/T]AAGAATAGTGATTTT | 10477 |
rs549696204 | in-del | -/TCT | 0.00795532 | 0.062565 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025697 | ATTGGCTATTAATAA[-/TCT]TCTACAGTCACATCT | 10477 |
rs549698728 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032269 | TATGGTCTTACTCAC[C/G]TGGTAGCAATTGCAT | 10477 |
rs549713260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057384 | TATGCATGCTTGCAG[A/G]TTTAGAGGGGTGTGT | 10477 |
rs549758791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032932 | CTCCCATTCACAATT[C/G]CTTCAAAGAGAATAA | 10477 |
rs549759153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038669 | CACAGAAAGGGAGAA[A/T]ATAATTTGAAAACCT | 10477 |
rs549801845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996675 | GGAGGGGCTGTCACT[G/T]GGCACTTGCAAATTA | 10477 |
rs549818179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037203 | GCTGCCAGCAAATAT[A/G]ATTATATGTAGTACA | 10477 |
rs549833367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044155 | TTTTTCCCAAGTACT[A/G]CAATTTCTGGTCTTT | 10477 |
rs549898843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994035 | ACTCAGAGACATGTA[A/G]TTTATATGGAATTCA | 10477 |
rs549938777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054323 | ATGAATCTAGATATT[C/T]TGCATTTCCTGTACC | 10477 |
rs549943959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050405 | CTGTTTTGTTCAACG[G/T]GATTCTCTTCAGAAA | 10477 |
rs549977057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051028 | GTTTCTTCGTACTTT[C/T]TTCCCAGTCTCATTC | 10477 |
rs549982168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043280 | ATAAGAAAATGAATG[C/T]TTACTAGTAGCATAT | 10477 |
rs549982549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021337 | TAACCTCACCATTAC[A/G]GTGTTTCTTCTTTTC | 10477 |
rs549993477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008867 | AGTGACCGTGATTCT[C/G]TGTTGCAGTCTTTGA | 10477 |
rs550044792 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042884 | GAGTAATTTGCACAA[C/T]GTCACACATCTGGTA | 10477 |
rs550045295 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022206 | TTTTTATGAATGTTA[A/G]TAGTTATTTTATAGG | 10477 |
rs550055380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049098 | GGAGTAAAGAAGCTT[C/G]AGAGGATAAAGATAT | 10477 |
rs550076717 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034482 | AATTGAACAATGAGA[A/T]CACTTGGACACAGGA | 10477 |
rs550094592 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027919 | AACATTTTTTGAAGC[A/C]TAACAGTAACACAAT | 10477 |
rs550096559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020942 | GATAGGAAAGGGGAA[C/T]TTTTATCCTTCCTGT | 10477 |
rs550163702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056752 | TTTTGATAAGAAGCA[A/G]GATATTTGCCTGGTC | 10477 |
rs550175435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997526 | ATTCTTTTTTCACCC[C/T]TGTGTTGTTTATCCC | 10477 |
rs550283580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002953 | AGAAAACTCAACACC[C/T]GGTACAAAAATGCAG | 10477 |
rs550298613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008098 | CAGTTTAAAGTTGGG[C/G]CTGGGTGATAAAAAT | 10477 |
rs550404847 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058862 | CACCATTTACTCTCA[A/G]TTACAGCTGTTAGTG | 10477 |
rs550511475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009995 | GATATTTTAAATACT[A/G]TTTCTGCTTTGTTTT | 10477 |
rs550515930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024412 | AAGGAAGGAAAATTC[A/G]GTCAAGTATTTTGGA | 10477 |
rs550518574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992239 | ACTGGGTTGTTTTTC[C/T]ACTTTGCTTTCAAAT | 10477 |
rs550578601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045818 | TCCACTTCCCTTATT[A/T]ATTTAGTGAGCCAGT | 10477 |
rs550612375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993465 | AAAATAAAGACATCT[C/G]TAGTCCAAAATTGCT | 10477 |
rs550699267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992982 | CATTTATATATTTCA[A/T]TTTAAATTGATGACA | 10477 |
rs550714002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988187 | TAAAGTGGCCACAGC[A/G]AGATAAAAATGGGAG | 10477 |
rs550729594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023480 | ACCTTTCATTTGATA[A/T]TAAGGAGTTTGCTAC | 10477 |
rs550766048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985675 | CAAGTTAAATTTGCT[A/C]CCTGGAAGAATCACT | 10477 |
rs550820174 | in-del | -/GTG | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031278 | ATGTTCATTTATTAT[-/GTG]GTTCAGATATTCTGT | 10477 |
rs550826308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035233 | AGTAAAACCTACACC[C/T]ATTATACTATGATTT | 10477 |
rs550826940 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003357 | CAGTACTCATGTTTC[A/G]GATGACCTCTAATGA | 10477 |
rs550883309 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043660 | AGAAAGTAAAATATA[A/G]TAATTAACGATAATC | 10477 |
rs550896426 | in-del | -/T/TT | 0.277067 | 0.24853 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041447 | GTGCAACATAAGGAA[-/T/TT]TTTTTTTTTTTGAGA | 10477 |
rs550904730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998082 | TAGTTGAAAGTAGTT[C/T]TGAAACTTGCCAGAC | 10477 |
rs550905684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030880 | ACAAGGTTTCTATGT[C/T]TTATTAGTCTTGACC | 10477 |
rs550965538 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985121 | TTGTGTATGTTAACT[A/G]GATCCTCAGATAAGG | 10477 |
rs550979497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004596 | CGAGATTGTGCCACC[A/G]CACCCCAGTCTGGCG | 10477 |
rs550999440 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987110 | ATGTTATTTTAAATG[A/G]TTTTAGGTATTGGAG | 10477 |
rs551003549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987406 | AAAGGTACTGGATTT[C/T]TAACTTAACCCCTAA | 10477 |
rs551009646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041657 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTA | 10477 |
rs551028467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022678 | ACAATGAAATTACTA[A/T]CAAAAAGCACAAAAA | 10477 |
rs551037021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010522 | GGATATTTGCATATT[C/T]ATAGATTCTGCCTAT | 10477 |
rs551041739 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013860 | ATGGAGGAATGGCCA[A/G]GTTCTGAAAAAGCAT | 10477 |
rs551050952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023370 | TAAATAGAACATCCT[C/G]TACTTTTGTCTTCTG | 10477 |
rs551055699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985557 | GTATGTGACTTGCAT[C/T]GTATTTCTATTGAAC | 10477 |
rs551085134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030084 | TGATCCACCTGCTTC[A/G]GCCTCCCAAAGTGCT | 10477 |
rs551094635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985022 | ACCTGTATTTTTGCT[A/G]CAAGTTGTATTCACT | 10477 |
rs551162276 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181043938 | TGGACATTTAAGTTA[C/T]TTTGAGTTTCACTAT | 10477 |
rs551187804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040713 | CAGTTTAGTCTGATG[A/G]CAAAGGAAATCACTT | 10477 |
rs551201631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039892 | ATACTTTGATTACTT[A/G]TAATACCAAATACAA | 10477 |
rs551202316 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001407 | ATACAATTATGTTTT[G/T]CCTTGAGTCCCAGAA | 10477 |
rs551231268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004889 | TGTTTGTATGATAAA[C/T]CTTCAGACAGACAAT | 10477 |
rs551267140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046280 | GCAGGTCAGGGATTC[C/T]GTGTAGGCATTAAGG | 10477 |
rs551467467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004538 | CTCGGGAGGCTGAGG[C/G]AGGAGAATCACTTGA | 10477 |
rs551528832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004078 | GGTCTTGGAGAGGCT[A/G]GGGTGGAGAGTTAAG | 10477 |
rs551538451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028647 | TGCATTTCCTAATAA[C/T]GAGGTTGAACAATTT | 10477 |
rs551551817 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024285 | AAACTTAAAGTGAGC[C/T]ATGAATTAATGTTAA | 10477 |
rs551599365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034250 | TATTGTGGCAGTATT[C/T]ACAGTAGCAAAGACT | 10477 |
rs551608428 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028721 | TTTTGTTATTTGTCC[C/T]CCTGCCCCCAATTTT | 10477 |
rs551608752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997465 | AATGTGTCTTCTTTC[G/T]CCCACTCTCCTTAGT | 10477 |
rs551611399 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041525 | CTCACTGCAACCTCT[A/C/G]CCTCCCAGGTCCAAG | 10477 |
rs551671811 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046843 | TCTGTAGTGCCTTTA[C/G]AGCACTCTTAGTGCT | 10477 |
rs551704150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009058 | AACATAAACAGATAA[A/C]CATTTGTATAAAATC | 10477 |
rs551734186 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047297 | TCTCATCTCAGGTAT[A/C]ATCTCGCCTTCTTAC | 10477 |
rs551809237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992440 | TGTGTTGTGATTACA[A/G]ACAAACCTAGAAGGC | 10477 |
rs551810819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047126 | ACATGACTAGATGAC[A/G]TCTTTAGTTTCTAAC | 10477 |
rs551823631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034599 | AGTTAATGGGTGCAG[C/G]ACACCAACATGGCAC | 10477 |
rs551832563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016538 | GCTTATGTCAGACTC[A/G]TTTTACAGTTTAGCC | 10477 |
rs551859245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998834 | AAAAAAATCGTCAAC[A/G]GCAGTTCCTTCAGAT | 10477 |
rs551865830 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990076 | TTGGGCATTTTAATT[A/G]GAATCTGGAAGCTGA | 10477 |
rs551934793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039358 | TGGCTACATTGAAAA[C/T]GTAATGAATATACTT | 10477 |
rs552021146 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994709 | TATTGGAAAAATATT[C/T]AGAGATTTACAATTT | 10477 |
rs552045881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045767 | GGTTGCTTATTAGAA[C/T]AACCTGGGAGATTTT | 10477 |
rs552056414 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051917 | CCTAAAATTTTGTAT[C/G]TGTTTTTAAGTCAAA | 10477 |
rs552083992 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992817 | TAGGCATGTGCCACC[A/G]CACTCAACTAATTTT | 10477 |
rs552089914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030363 | CTGTCGCCCAGGCTG[G/T]AGTGCAGTGGCACGA | 10477 |
rs552119539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051091 | CTGTATTTTTGGTCC[A/G]TGATTTCTGCATGTT | 10477 |
rs552180872 | in-del | -/ATC | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052721 | AGTTTGTAGTTTCTA[-/ATC]ATATCAAGACCTAGT | 10477 |
rs552314106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019476 | CTTGGCGGTTGTTTC[A/G]TCTTGTTACTTTGGA | 10477 |
rs552337396 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059090 | GATTATAAATTTAGC[A/G]TGTTGGTTTTTTGCT | 10477 |
rs552347089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061981 | GAATGTGACAACTCT[A/G]TATGAACTAATAGGG | 10477 |
rs552368783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017568 | TGGAAATGCGGTAAT[A/G]TGCATACCATCCTTT | 10477 |
rs552409186 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979545 | AATCCACAAATTCCT[C/T]TGAGGCTCCATCACC | 10477 |
rs552438200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059785 | TAGTGTGTTGGTCCC[C/G]TACCCCCTCCCTGTC | 10477 |
rs552472801 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037402 | TGTGTATGTTATTGC[C/T]CATGAGGACCCTACA | 10477 |
rs552549860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994388 | TTCATCTATGCCTCC[A/G]TCCATTTCACCCTCC | 10477 |
rs552670865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989709 | ATTAAGTTCAATGCA[C/G]ATAATGTAATTAGAA | 10477 |
rs552735945 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025871 | AACTCTCTAAGATAG[C/G]TCTACTTTATATGGA | 10477 |
rs552772057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004370 | CTGAGTGTGGTGGCT[C/G]GCACCTGTAATCCCA | 10477 |
rs552799125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031516 | CTCTGTGTGTTTTTA[C/T]TTATTTAGTCTGACA | 10477 |
rs552836552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058530 | TCAGCAGGTAAAAAC[C/T]ACTGGAATTAAGCAT | 10477 |
rs552840122 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996882 | TGCAAAAAAAAATTT[-/C]TTCCTCTAGCCCTTT | 10477 |
rs552850659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057888 | AAATCGGTTATTCTA[C/G]AACTTAAATGTGTAT | 10477 |
rs552904311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011510 | AGTTTTGGAGGGGAC[A/G]TTCAACCCATATAAC | 10477 |
rs552911701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000699 | AGCTGGGACTACAGG[C/T]GCCCACCACCACACC | 10477 |
rs552929739 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001056 | AATATGACACACTGA[C/T]TCTTAAAGAGGCAAA | 10477 |
rs553027599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985856 | GTGCATAAATCTAGA[G/T]AGCCTAGTAGACATG | 10477 |
rs553052827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039528 | GTAATCCCAGCACTT[A/T]GGGATTTCGAGGTGG | 10477 |
rs553084565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017682 | CGGAAGTGTCATATG[C/T]TGCTTATTTAACAAC | 10477 |
rs553147590 | in-del | -/AAG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983024 | TCTGATGGAGAAAAA[-/AAG]ATTCTGTCAATGAGA | 10477 |
rs553158821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016716 | GTCTCACGACTATTA[G/T]GATTTACTAGAAATT | 10477 |
rs553172091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | UBE2E3 | GRCh38.p7 | 2:180987452 | GAAGAAGCACAAATA[C/T]ACTGACGAATATTTT | 10477 |
rs553210877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986874 | CAAAATTATTCAGAC[A/T]GGGATGATTTCTCTA | 10477 |
rs553266603 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037304 | ACTCCTTATTTTTTT[A/G]AAGTTAACTCTAAAA | 10477 |
rs553284486 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985445 | AAAAGTTCATTAATA[A/T]TAAAATAATATTTTG | 10477 |
rs553425700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031178 | CTAATGTATTGTTAG[A/C]TTTTATACATATGTC | 10477 |
rs553455408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061610 | AATGATAGCCAATGA[A/G]AATTGAACTAGATTA | 10477 |
rs553462389 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044783 | TGTTAAAAGTCTTAA[-/TT]GCTCACTAGTTTCTG | 10477 |
rs553466266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024479 | AAGCAGATTAGGTAG[C/T]GCTGCAATAAATTAA | 10477 |
rs553483836 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019092 | CCTCAGTCTTCCAAG[G/T]AGCTGGGACTACAGG | 10477 |
rs553491869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060393 | GTGTATGCAAACAGA[C/T]GTACCCACACACATA | 10477 |
rs553500124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025536 | GGGTATTCTTTTAGA[A/T]GACTTGTCTAAGTTG | 10477 |
rs553508715 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980851 | GAGCCTCCTCGGCTT[C/T]TTTTTTTCCCTCCCC | 10477 |
rs553588066 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006691 | AAGAAAGCAGAGAGA[-/T]TTTTTTCTATATTTT | 10477 |
rs553599671 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026567 | AAAGGCTGAGGAAAC[-/AG]AAAGTGAGAGAGGGG | 10477 |
rs553608715 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014025 | GTTGTAAGAAGTAGA[-/T]TAATACAAAAGGTGT | 10477 |
rs553633234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999419 | AAATACACATCTGTT[G/T]GAATACGTGGTTTTA | 10477 |
rs553763208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000431 | GTTAACACTGTACAA[C/G]TCCAGGGGGTACCAT | 10477 |
rs553797579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047416 | CCAGGCCCCTTTATC[C/T]TACTTGTCTGTCTCT | 10477 |
rs553807145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020229 | GCTCCCTCTGAAATC[C/T]GTAGGGGGAGCATCC | 10477 |
rs553865280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037292 | ATTTTAGAGTGTACT[C/T]CTTATTTTTTTAAAG | 10477 |
rs553876582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994730 | TTTACAATTTGAAAG[A/G]AACTTGCAGGTGAAT | 10477 |
rs553879682 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024399 | AAACATTTTCAAAAA[A/G]GAAGGAAAATTCAGT | 10477 |
rs553900250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000796 | CCTGATCGTGTGATC[C/T]GACCACCTCGGGCTT | 10477 |
rs553917011 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004112 | TATCTAATACTGTGA[A/T]GTTAAATTTAATCAG | 10477 |
rs553971768 | in-del | -/TTTA | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981268 | CTTCTTGGGGCTTTG[-/TTTA]TTTGTTTGTTTTTTC | 10477 |
rs553974156 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055682 | CTGCAATAGTTAAAT[A/G]TACACTTTGTCCTAT | 10477 |
rs553974221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048572 | TAGGAAGATAAAATC[A/G]TGGGAACCACTAGCA | 10477 |
rs553994981 | snp | A/G | 0 | 0 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042474 | TTCTATTTATTAATT[A/G]AATTCAGATAAAGAA | 10477 |
rs554015946 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035956 | TAAAGTAAGCCTCCA[A/G]TGTGGTAAGTGATGT | 10477 |
rs554078605 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057398 | GGTTTAGAGGGGTGT[C/G]TGTTTCGGGAGAGAG | 10477 |
rs554098953 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027768 | AGCTAAGCTTTCTTT[C/G]CTGTCACTCTTAACA | 10477 |
rs554117157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996182 | ATATGGACCTATTTG[A/G]TGTATAACAATGCGA | 10477 |
rs554191137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032658 | CCATCTCTTTGAAAC[A/T]CTGTAATTTGGACAT | 10477 |
rs554210407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035480 | TACTTTCAGTAGATG[C/T]ATTATATATTACTCT | 10477 |
rs554221263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002020 | TATGGAGATTGAAGG[C/G]CTTGAATATCCCAAG | 10477 |
rs554252894 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010133 | GAAAGTCCACCACAT[A/G]CTACTACTCCTACCA | 10477 |
rs554269166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030676 | AAGTCTCCTGTAAAA[C/G]TATGTGGACCTGGTG | 10477 |
rs554363096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006615 | AATTTAACTGAGTAG[G/T]TTCTGTTTTTCTGTA | 10477 |
rs554365025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013771 | CATACAGCATCACTT[A/C]TGCTGCTTTTGTTGG | 10477 |
rs554379002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050049 | AGGCCAATAAGTTAC[A/C]CAAGCATTTGTAGTA | 10477 |
rs554382435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040389 | ATCCCTACTACAGTG[C/T]CTGGCTTATGATGTA | 10477 |
rs554416546 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060166 | TGATTTTACCAACCG[C/T]CTTCTAAATCCTCCA | 10477 |
rs554428180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013249 | TTACCCCACAATTTA[A/G]TGGCTTTAAATGGAA | 10477 |
rs554452535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062205 | CTATGGTTTGGTACA[A/G]TTCAAATATTGTACC | 10477 |
rs554481118 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019842 | TAATTTTTTTCTTTT[G/T]TTTGTGGTGAGAACA | 10477 |
rs554513996 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053391 | GTGTTTCAAGTTCCA[A/G]AATACCTGATTTCAG | 10477 |
rs554538316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031128 | GGCCTCTCATACTAT[A/T]TTTTTAAAAAATTTG | 10477 |
rs554545330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004807 | GTAATATATATATAC[A/G]TAGTAGGTGACAACT | 10477 |
rs554552151 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031034 | TTGTAATTTTTTAGA[C/T]TGGGTTCTTAATTTT | 10477 |
rs554592073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024831 | AGAAATGAAATAAGG[A/G]TTTTTTTTTAACTTA | 10477 |
rs554595082 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016594 | TATAAGTAATGGAGG[G/T]AGAATCCCAGCTCAA | 10477 |
rs554653588 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033223 | GCCCGCATTGCCAAG[A/G]CAATCCTAAGCCAAA | 10477 |
rs554668049 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044854 | AGAATATTTTATGGC[-/ATA]GTAGTTATATAATGT | 10477 |
rs554727904 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018859 | TTTTCCTCATAAACA[-/AT]TACCTGAGTTGGATG | 10477 |
rs554778229 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023441 | CAATGATATTTGTTA[C/G]AAATACTTAAAATTA | 10477 |
rs554789182 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037663 | CAGAAAGTTAAAAAA[A/G]AATTTTAAGTTGACA | 10477 |
rs554790099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047972 | CATTGTACTTCCCAT[A/G]TTCTCTTCCCTTCTG | 10477 |
rs554832062 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061431 | CCCGGCCGACCACTT[A/C]TAACAAGAGTAAAGC | 10477 |
rs554890442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054449 | TAGGTGTGTAGTGGC[A/G]TGCTTTTCTTGTTTT | 10477 |
rs554915166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001461 | ACTGTGAATGTAGAG[C/G]GTGGGACATCAAGAA | 10477 |
rs554927591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058050 | ATTGTAAATAAAACT[A/G]TACCTTGCACATCAA | 10477 |
rs554932501 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049450 | GTTGTACTTGTAGAA[A/G]TGTTTTCATCTACAT | 10477 |
rs554960789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021098 | GGGAAAGGTGGTTTA[C/T]AGAAATAGGATAATA | 10477 |
rs554960811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013980 | ATGCTTCTAATAGTC[A/T]AGGAAGGATTTGATG | 10477 |
rs555050708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041585 | CTGGGATTACAGCAC[A/G]CACCACCATGCCAGG | 10477 |
rs555070420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055182 | GTAGATAAGATTTCC[A/T]AGGAGTTTTGCTGTC | 10477 |
rs555073501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020486 | ACATTATCTTTTAGG[A/G]GCCTACAATTCAAGC | 10477 |
rs555094621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049479 | ATTTATATAAGTGTA[A/C]AGTACTTTGCAATAA | 10477 |
rs555138779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013213 | CCATAGGAGTTGTGT[C/T]ATCTATTGCTACTTA | 10477 |
rs555165584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990525 | CTATGCGTAGTTTAC[A/G]TATGTCTTATATTAT | 10477 |
rs555168123 | snp | A/C | 0.000163659 | 0.00904448 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984142 | TTGTGGAAAAATACC[A/C]AGAGATTGATGTATT | 10477 |
rs555202434 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990130 | TCTTTTGCCTTTTGA[G/T]CAGTGGTTCTCAACT | 10477 |
rs555202704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996102 | CATCTTTATAGAATT[C/T]CTTAATTTAAAAAAA | 10477 |
rs555216819 | in-del | -/TTTTTTTTT | 0.0962929 | 0.197165 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs555220308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019003 | AGTTTTGCTCTTGTC[A/G]CCCAGGCTGGAGGGC | 10477 |
rs555242261 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980504 | GAGCGCGCGGGAACA[C/G]CTCGCGCCCGCCGGG | 10477 |
rs555274378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026271 | TTAGTATAGCAAATA[C/T]AGATTACATATTCTG | 10477 |
rs555337631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032023 | TCTGCAATGGAAAAC[C/T]AGCTTCAGGGAGGTG | 10477 |
rs555350376 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007125 | AATCATTTTTTTTTC[C/T]AGTAGTCTGTGGTGA | 10477 |
rs555376197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001985 | GTTTACAAAGAAGTT[A/G]TAGTTTTCCAGCTGT | 10477 |
rs555413370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028732 | GTCCCCCTGCCCCCA[A/G]TTTTGTTTTATTAGG | 10477 |
rs555429052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056947 | ATACTATTTCAGCCA[A/G]ACACCTACTATTTCA | 10477 |
rs555466126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028886 | AAATTTATCAGTCTC[G/T]TATATGATTAGCACT | 10477 |
rs555473001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983317 | TTGACATAATTTAAA[A/C]TTCTCAATTTGGTAT | 10477 |
rs555504376 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063277 | ATTAAACCCAGATCT[A/G]TTTCTGAGTATGTGG | 10477 |
rs555663489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036942 | TTGCAGTTTCCAAGA[A/T]CCTATCCACAACATT | 10477 |
rs555791072 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030836 | TATTTTTTTCATGTC[C/T]GTTATTTCTGTCTTC | 10477 |
rs555839036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013405 | GAAGACTTGATGAGA[C/T]TGGAAGATCTATTTT | 10477 |
rs555855865 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983182 | AGAATATAAAAACTG[A/G]TCAAATATTGCATTC | 10477 |
rs555861773 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047563 | GCAGTCTGAAAACTA[C/T]AAGCTATTCTCGAAA | 10477 |
rs555900219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997561 | CATCTCCCCTAGGCT[C/G]TCATGCCACATTGTA | 10477 |
rs555921165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055241 | AAGGGAGAGAGAAAT[A/G]GAGATTTTAAAAAAT | 10477 |
rs555976814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043710 | TTATTTCCACCCATC[C/T]TCTTTTAAAATACAC | 10477 |
rs556024215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001361 | CGAAAGTAGAATTTT[C/T]GAGCTTCTTAAATGG | 10477 |
rs556062200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989372 | TGTTAATAAATAAAT[G/T]GAAGTCTCTCAAATT | 10477 |
rs556086955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000999 | GCATCATCAACTCAT[A/G]TCAGTAATGAAGATA | 10477 |
rs556088521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031372 | ACTTTTTATTTATAT[A/G]TTGCTGTATAATCTT | 10477 |
rs556115935 | in-del | -/TAAG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001912 | GACTGTCTTTACTAT[-/TAAG]TATTTGTTGACGAAA | 10477 |
rs556153748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035942 | GAACTCTATAGGTAT[A/C]AAGTAAGCCTCCAAT | 10477 |
rs556155162 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063095 | TAGTTATGTTTAAAA[C/T]GCCTACTTGCAAGTC | 10477 |
rs556211326 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033018 | CAAACCACTGCTCAA[C/T]GAAATAAAAGAGGAC | 10477 |
rs556212650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983048 | TCAATGAGACTCTTA[C/T]CAGTGGTAGTAGTAG | 10477 |
rs556241381 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048849 | CTACCTGTGTTCTCC[A/G]CCTACTTCACACATG | 10477 |
rs556246708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982302 | TGGTTGGACGCTTTT[G/T]TTGGTTTTACCTCAA | 10477 |
rs556276642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033790 | TACCCATCTGACAAA[A/G]GGCTAATACCCAGAA | 10477 |
rs556291040 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053177 | AGTGAATACCTGCCA[A/G]CTACATGAACTTTGA | 10477 |
rs556315112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031871 | GTTTAATTTTAATCA[A/G]CTCCTTTCCTGATTA | 10477 |
rs556329063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036463 | GGGCCATTGTGTGGA[C/G]TTTGCATCTTCTCCC | 10477 |
rs556386399 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991407 | ATCCAAACTGCCAGC[A/C]TCACTACTCTTGGGC | 10477 |
rs556398381 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049422 | TTTTTTAAATTATTT[A/C]ACCTTGTGTATGGTT | 10477 |
rs556443146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007698 | TGGAGGGGGCCCAAC[A/G]GTGAATGGAGGCCAG | 10477 |
rs556449255 | in-del | -/CCT | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983690 | TATTCCAGTGCTTTC[-/CCT]CCTCCCTTTTTGTCT | 10477 |
rs556465228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042166 | TACCCTATCCCCATC[A/T]GTCATTCTAAGCTTT | 10477 |
rs556496858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991029 | ATTACTGTTTCCACA[A/C]CAAAAATGTATTAAT | 10477 |
rs556509314 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048896 | TGTACTTCATATAAT[C/T]AAATTTGTTCTGCAT | 10477 |
rs556519478 | in-del | -/TCTT | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021470 | CTCTCTTTCTTTTTC[-/TCTT]TCTTTCTCTCTCTCT | 10477 |
rs556693029 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055908 | TCTTGTTTGTATTTT[A/G]TAAAGTAATGGTGTG | 10477 |
rs556757108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002086 | CATTAGCTAGAAATA[C/T]ATATGGCCTTCCACA | 10477 |
rs556757595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009249 | GATGCTAAGAGATTG[A/G]ACACATTATAAAACA | 10477 |
rs556802597 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058399 | AGTATGAATTAGATG[A/G]ATAACAGAGAACGGG | 10477 |
rs556829818 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034677 | AACTTAAAGTATAAT[-/A]AAAAAAATTAAAAAG | 10477 |
rs556846978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012991 | TCAGGAAGACATGCA[C/T]ATTAATTTTTTTATT | 10477 |
rs556852290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013924 | AAAATACAGTTTGCT[A/G]CAGAAGGGAGAGCAA | 10477 |
rs556978085 | in-del | -/GGGGTGAGTTG | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058411 | TGGATAACAGAGAAC[-/GGGGTGAGTTG]GGGGTGAGTTGTGCC | 10477 |
rs556985458 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993583 | ACTTATAAATCATCA[G/T]CATGATCCCCCTTTA | 10477 |
rs557014859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991366 | AAATTAGGCACAGCA[A/G]GAGATTAACAACTTC | 10477 |
rs557041182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050741 | GCTCGGTTTCTCATC[C/T]GTGAAATTGTGATAA | 10477 |
rs557064347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023620 | CTCTTTAAGTAACTC[G/T]ACTCTGACAACCTCG | 10477 |
rs557070182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015573 | CAGAATTCTTGGAAA[A/C]ATGAACAGTTTTCAT | 10477 |
rs557120139 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996086 | AGTATATTGCTGTTA[C/T]CATCTTTATAGAATT | 10477 |
rs557124388 | in-del | -/TTTCTC | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031612 | CGACTACTTTCTGTT[-/TTTCTC]TTTCTGCGCCCCTCC | 10477 |
rs557156246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057578 | TTTCTTTTATACTTA[C/T]TTTACTTCTTATTGC | 10477 |
rs557159463 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981661 | TTAGTGACTTTTAAA[A/C]ATTTTTCAGCGAGAT | 10477 |
rs557212687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986694 | AATACATTTGGCTTT[C/T]GTGTGTAGTTATTTA | 10477 |
rs557219698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999063 | AAACTTGTTTTGAGG[A/C]AAATGTAGTATGAAT | 10477 |
rs557232101 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998459 | TGGGATAAGGAGAGT[G/T]GGGAAGGGGCAGGGG | 10477 |
rs557260007 | snp | G/T | 0.000925336 | 0.0214898 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984119 | AATTTTGTTGTTTTG[G/T]TTTCAAATTGTGGAA | 10477 |
rs557262540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984384 | AGAGGGTGTTTTTTC[A/G]GAAGTATACTGAAGA | 10477 |
rs557265723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029534 | CTAGGAGTTTAATAT[G/T]TTTGATGCTTTTGTA | 10477 |
rs557322559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021178 | TTGCGACTACGAAAC[A/T]TGAGATTAGTCAGGA | 10477 |
rs557337013 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046929 | TTAAAAATTACACAG[-/A]AAACTATTCAGAGTA | 10477 |
rs557362153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052240 | TAGGATGTTGGTGAT[A/G]TCAAGAATTAATTAA | 10477 |
rs557406079 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978962 | AGCTTCAACTCCAAA[C/T]TGGCTGGCTTTTGCT | 10477 |
rs557442766 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978434 | TACTTCTTTAATACA[A/G]CACTTCTCATTCTGC | 10477 |
rs557594862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992043 | CTTACTACTCATGAT[A/G]AAAGGGTATTTTCAT | 10477 |
rs557604682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021904 | AAAGTTTAGAGTAAA[A/G]GTGCCCAGAATCCTT | 10477 |
rs557647498 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044476 | AAAAAGAATCTTTAG[A/T]GGCAATAGAGAATAC | 10477 |
rs557652881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039457 | AGAATGCCTGTGGTC[A/G]AATGTAAAAACATTG | 10477 |
rs557673480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990610 | GTACTTGCTAAATTA[C/T]GGTCTTCTGAGGCCA | 10477 |
rs557717947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035674 | CTTCCTTGAAACATT[A/T]TTAGATTTTTTTTGC | 10477 |
rs557798400 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991933 | TATTTTTGGACTGTG[A/G]TTGACCTAGAGTAGC | 10477 |
rs557800171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029023 | TTCTTTGAAAAGGGT[A/C]AGGTAGTAGTCCAAT | 10477 |
rs557861506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005765 | GCTTTAATCTTTTGT[A/G]TATGTATTTAATATT | 10477 |
rs557862508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023576 | CCTTACTTTCTTTAA[C/T]ACAGCCGCCTGATAG | 10477 |
rs557866440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014734 | AAATTTTTATTGATA[C/T]AGTTATACATGTTTT | 10477 |
rs557891682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056966 | CCTACTATTTCAGCC[A/G]GAAATGCGTTACATG | 10477 |
rs557915055 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034426 | GCAAACTGTTGCAAG[A/G]ACAGAAAACCAAACA | 10477 |
rs557926669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021147 | TCTTCGTGGGCTTTC[A/C]CATATAGTAATGTAG | 10477 |
rs557972847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033970 | TGCAAATCAAAACCA[C/T]AATGAGATACCATCT | 10477 |
rs557973139 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042741 | AACATCCATAATTGA[A/G]TCCCAGGCCAAATGT | 10477 |
rs557995921 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027372 | TATCATGGTCATCCA[A/G]ACCTCTTGTTTTAAA | 10477 |
rs558011452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003674 | TGTTTGCACATAGTA[C/T]ACTGTGGAACCAGAC | 10477 |
rs558038683 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998262 | TATAAATTGGTGGTG[G/T]TCTGGTTGGACTTGG | 10477 |
rs558053780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026770 | ATATGGTTATACTTA[G/T]ACTTAATTTACACAT | 10477 |
rs558122350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045203 | GAAGGTTGTAGAGAC[A/G]TTTTCTCATTTGATC | 10477 |
rs558139433 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022992 | AAACCAGATAGTCCC[C/G/T]GACCAACAGTGGTTC | 10477 |
rs558165849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058761 | AAACGGATTTATTTT[A/G]TGAATAAAAGAGGGT | 10477 |
rs558239812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985962 | TGTTTCCTCAAGGTC[A/G]CTGAGGATTATTTTA | 10477 |
rs558246807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993107 | GACATTCTATCAGTT[A/T]TATAAGGGTGTATAG | 10477 |
rs558248604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046365 | TCCATACCTGCCCTC[A/G]TATATCAAACTGCAA | 10477 |
rs558360787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052817 | TTTCTTTGTTCTGCT[G/T]CTTCTGCCTCTGCTG | 10477 |
rs558570044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030207 | TAAACTCTTCATTGG[G/T]CATTAAATTTTAATG | 10477 |
rs558599181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059225 | TGGTATAATCTTGGT[A/G]TTTGGAACAATTATT | 10477 |
rs558632510 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049585 | TGATGACTGTCATAA[G/T]AGGCCTTAAGATAGA | 10477 |
rs558732237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004773 | CTAAGGCATCATAGC[C/G]TCCTATATTGTGAAA | 10477 |
rs558744930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004431 | CGAGGTCAAGAGATC[A/G]GGACCATCCTGGCCA | 10477 |
rs558774782 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057547 | ACACATGCACATGCA[A/G]ACACATTGGGGCTTA | 10477 |
rs558781016 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979196 | ACTGTTCCCCTTCTG[C/G]ACTAGGAGCTCTTAG | 10477 |
rs558805112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053870 | CTTCCACCCCACTAA[C/T]CCCTGGCAACCACTG | 10477 |
rs558819296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011574 | AAACTAAGTCAAAAA[A/T]TTTTTAAGAAAAATA | 10477 |
rs558854325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034483 | ATTGAACAATGAGAA[C/T]ACTTGGACACAGGAA | 10477 |
rs558864279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987591 | TTTCAAGTTAATAGT[A/G]TTAATATATTGACTA | 10477 |
rs558882823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018436 | TACATATATATTTGG[C/G]CTAGGATTGTACAGT | 10477 |
rs558935155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012274 | CTAGTATATACTGTA[A/G]ATTTTCAAATATAAC | 10477 |
rs558966059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054376 | TGGATGAGAGTTCCT[A/G]TTACTCCACATTTTC | 10477 |
rs558993849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991619 | CAAACTCATAAACTT[C/T]CTTAAAACATGAGAT | 10477 |
rs559031474 | snp | C/T | 0.416871 | 0.186156 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061113 | ACAGACCACTTCTTT[C/T]TTTTTTTTTTTTTTT | 10477 |
rs559038394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047959 | CATTAGGTCGTTTCA[A/T]TGTACTTCCCATGTT | 10477 |
rs559045615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018871 | ACAATTACCTGAGTT[C/G]GATGTCAGGATAGAT | 10477 |
rs559238283 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003341 | ACAATCTTGCCATTA[A/G]CAGTACTCATGTTTC | 10477 |
rs559288723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022625 | TGCACTTAGAAACAC[C/T]AGATAGCACTTTAGC | 10477 |
rs559311145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044449 | CCCAGATCATAAGGG[A/T]TAGAAGTGGAAAAAA | 10477 |
rs559377697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050899 | CTTTGAAACTTCCTT[C/G]TTTCTTGTTTCAACG | 10477 |
rs559438236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034517 | GAACATCACACACCG[A/G]GACCTACCGTGGGGT | 10477 |
rs559445749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999251 | AGTACTCTGACGTTC[C/T]ACAGTAGGCTAAAGA | 10477 |
rs559452285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038982 | TGAGAAGGCAAAATG[G/T]TATGGCCACTTGGGA | 10477 |
rs559474207 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999237 | GAATGGCAGTTCCTA[A/G]TACTCTGACGTTCCA | 10477 |
rs559514767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009706 | CTAACTTCTACTTAA[C/G]TGATAATTGTGACAA | 10477 |
rs559518434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002810 | TCTTTCACTTATCTT[C/T]GATTATCTTTTGTTC | 10477 |
rs559527279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016497 | TCTTAATATTTCTTA[C/T]TTAATATGTAACACC | 10477 |
rs559535997 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019453 | TCAGTGTTCAGTGTC[A/G]TTTTTAACTTGGCGG | 10477 |
rs559562531 | snp | A/C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036415 | TGTATTGTACTTACA[A/C/G]CGTTCATGAGGAAAA | 10477 |
rs559588967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044046 | ATGTGGGATTACTTA[A/G]TCAAATGACTCTTGA | 10477 |
rs559604382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008581 | TGTTTCCCTGTTCCA[A/G]GCCATGCTCAGGGCA | 10477 |
rs559619980 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058664 | CATGGTGACTTTTGT[G/T]CTCTGTACTTTTAAA | 10477 |
rs559620322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037825 | AATTTAAAAATTAGC[A/G]GGCATGGTGGCATAT | 10477 |
rs559623536 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035319 | TTGCAGTAGTACTGT[C/G]AGCTGCTGATTTTTC | 10477 |
rs559664822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986044 | TATATACCAGATTTC[A/G]TTTAAGTCCTTGAAA | 10477 |
rs559692984 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042824 | GCTGTCAGCTTCACT[A/G]TAACCCCAAAGGCAG | 10477 |
rs559713020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015685 | TTTTAGGAAGTCACT[A/G]GGAAAAATCGACATT | 10477 |
rs559751907 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041134 | GTGCCTGTAGTCCCA[C/G]CTACTTGGGTGGCTG | 10477 |
rs559793962 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032198 | TTTTTTGTTGAAGTA[G/T]TGTGTTATGAAGGCT | 10477 |
rs559802791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045730 | TAGTAACCACATCAA[A/T]TAACTTAGTACCTCT | 10477 |
rs559824750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060125 | AGAAATAAAAGGCTA[A/G]GAAACAGAAAGGCAG | 10477 |
rs559889463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052310 | TAGGTTCTTGAAGTT[G/T]CTGTTTCTGGTTAGG | 10477 |
rs559902607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030779 | GTATTCACTTAGTCT[G/T]TTCTTTTTAGTAGGT | 10477 |
rs559954743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059449 | GCATTAATGGAAATA[C/T]AGTAAAATCTACATG | 10477 |
rs559954798 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051891 | GCTTTTTTATGCAGT[A/G]TGGCATTGTACCTAA | 10477 |
rs559974233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035163 | TTTGTTTTAATATTT[A/G]TATGCATTCTATATA | 10477 |
rs560031174 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030017 | TTTTGTATTTTTAGT[A/G]GAGACCAGGTTTCAT | 10477 |
rs560037891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034821 | TTCCATGAACAAATG[G/T]GGCTTTCAACAGGTG | 10477 |
rs560065794 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023122 | GAGTTCCTTGACTTA[C/G]AGTGGGGCCGCGCCC | 10477 |
rs560066327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058893 | TTTAAAGTGCTTTAC[C/T]GTGTGGTCCCATCAG | 10477 |
rs560092913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981875 | CCTCCCTTGTACGTA[C/T]CCCTGTTGTACGATG | 10477 |
rs560101707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018534 | CGAGGACTCAGGGGA[A/G]TATAGTAGTAAAACT | 10477 |
rs560151820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979947 | AAGGACACTTCCCTT[C/T]GGCAGCGACAGTTGC | 10477 |
rs560272308 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001408 | TACAATTATGTTTTG[C/T]CTTGAGTCCCAGAAG | 10477 |
rs560329773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025811 | CAAGTCTTCTATAAG[A/T]ACAATTCTAATGTCA | 10477 |
rs560333530 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014345 | GATACAACTCAGAGA[A/C]GCAGCCTGGGTTGGA | 10477 |
rs560333533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988574 | TGATTTTACTGTGAA[C/T]GGGATTATATCAGCA | 10477 |
rs560344027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036562 | AATTGGTGTGCCTAA[A/G]TTGTCCCCACCTGAG | 10477 |
rs560369970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987898 | GCTTCCCCCAACCCC[C/T]AACCCAGAATTTGAA | 10477 |
rs560374412 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984233 | TTAAACAAAAATTGT[A/T]GAAGGTGAACTAGAT | 10477 |
rs560418352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040575 | GAACTATAACATCTA[A/G]ACATTTAATGTTAGA | 10477 |
rs560456191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993321 | GAAGCTTTGAAAGGA[A/G]CTGTGGTGTAGTCTG | 10477 |
rs560516196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032111 | CATTCCCTGAAGAAG[A/C]AAAAGTTGCTAGTCT | 10477 |
rs560533931 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050267 | TGGCCATATTTGTTT[C/T]GAAGGTGATACCTTG | 10477 |
rs560541897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000626 | GTGGCTTGATCTCAG[C/G]TCACTGCAAGCTCTG | 10477 |
rs560688827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006136 | ACAGCAAGGCAGAAC[G/T]GGAGAGGGTAAGGAG | 10477 |
rs560694339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001048 | AGATGGAGAATATGA[C/T]ACACTGACTCTTAAA | 10477 |
rs560702657 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047970 | TTCATTGTACTTCCC[A/C/T]TGTTCTCTTCCCTTC | 10477 |
rs560706943 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027407 | AGACATAGTTAATCA[C/T]AATTAAAAATGCTAA | 10477 |
rs560799022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012829 | ATGTATAGGCATGAA[C/T]TTAGAGATACTAACA | 10477 |
rs560800867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005581 | TTTCTCCATAGTCCT[C/T]ACCTCTTCCTATTAT | 10477 |
rs560860662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017950 | GCTCAGTCTTCTGAG[C/G]GTGACTCTCTTTTTT | 10477 |
rs560861857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039257 | TTTGTCAAAACTTAG[C/T]AGTGTTTATTTCAAA | 10477 |
rs560868708 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020211 | AGATGTGGACAGGGC[C/T]GTGCTCCCTCTGAAA | 10477 |
rs560871140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017417 | TTAGGGGCATGAGGG[A/G]GGTGGAAACCAAGCA | 10477 |
rs560872176 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046120 | AATCAGTAAATGTTA[G/T]AAGAGTGAATCAGTA | 10477 |
rs560886941 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051759 | TTCTTAGGACTATTA[A/C]AATACTTAGTCCAAC | 10477 |
rs560964272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034777 | TTTTATTTCATTTCT[A/G]TTTATATTCAGGTTT | 10477 |
rs561025044 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036511 | CTCCGTGTATTCTGG[A/T]TCCCTCCTAAATTTC | 10477 |
rs561110402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025211 | CCAGACTACTTTGCA[C/G]AATTATACTTGAATT | 10477 |
rs561138411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992249 | TTTTCCACTTTGCTT[G/T]CAAATACTCTTTTAA | 10477 |
rs561241206 | in-del | -/ATTTGAATCAGTGCTGTCTTATTTACAT | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012346 | TTAGTTACAGTTGTC[-/ATTTGAATCAGTGCTGTCTTATTTACAT]TATTTTCTAGATAGT | 10477 |
rs561312423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031439 | TAGAGCAAGCTTACA[A/G]TGTTTCAGTAGCATA | 10477 |
rs561339383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005027 | AGTTACTTTTAAAAA[C/T]TGACTTTGAATGCCT | 10477 |
rs561474218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013461 | CTGTTGGCAGAAGGT[C/T]TCAGTTCCTCACTGG | 10477 |
rs561501727 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040835 | ATTGTTAGATCCAGA[C/G]AGTTAGACTGTGCAG | 10477 |
rs561537017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020053 | TTTGCATCTCTGAGT[G/T]TGACTACTGTATTTC | 10477 |
rs561538149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012995 | GAAGACATGCACATT[A/C]ATTTTTTTATTTTTT | 10477 |
rs561554872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047562 | AGCAGTCTGAAAACT[A/G]TAAGCTATTCTCGAA | 10477 |
rs561631059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048284 | GAAATCTCCATTGTA[C/T]ATTTAGTTTCTTGTA | 10477 |
rs561633108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060105 | CAAGACAGTGAACCA[C/G]CTGTAGAAATAAAAG | 10477 |
rs561681290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001703 | TGAAAAGAGGAGCTG[A/G]GATTTCGAAGGTGAC | 10477 |
rs561693758 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058811 | GTCTAACAAGGTAAC[A/G]AGTGCCATCTAGTGG | 10477 |
rs561694422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995822 | CTGGTGTGCTTTTCT[A/G]TCAAAAGGCACCTAA | 10477 |
rs561696809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054845 | TAAGGTCTTAGCTCT[A/G]GAGGACTGGTGATAT | 10477 |
rs561742730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006749 | GGGTCCTTTCATCAT[A/G]AAGCAACCCAACCTC | 10477 |
rs561768530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055432 | TGCAACTGCTCATGT[C/T]CCTTCCTGACCCCTT | 10477 |
rs561827567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056595 | CTGAGGGAGGGCATT[A/G]ATTTATTCATGAGGG | 10477 |
rs561878303 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980169 | GACTCCCAACCACGC[G/T]CCCAGGGCCCTTGCC | 10477 |
rs561889343 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063726 | TGGCTCGCTCACTCA[A/G]GAATCTGGTAATGTC | 10477 |
rs561902409 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038492 | AATGGGTCATTGACC[A/T]AAATGTAGGAGCTAA | 10477 |
rs561940432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061867 | CTCGGCAGAGATACA[C/T]ATGCAATAGATAGTG | 10477 |
rs561948517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021209 | TTGTGATGTTTTTGC[G/T]GACAAATAAGATATT | 10477 |
rs561978256 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022349 | TTCTCGGTGGTGTTA[C/T]GTTCCATAAAGTTGT | 10477 |
rs561979171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981628 | GACCAATGTCAGTGT[C/G]TAAATATTTAGACGT | 10477 |
rs561982730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025635 | GGACTTGTCTCAGAA[A/G]TGAGGGAAATATAGG | 10477 |
rs561992162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032814 | AAAATCTCCTTAAGC[C/T]GATAAGCAACTTCAG | 10477 |
rs561997931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984470 | TGACCTTCCACATTT[A/G]GAAATTGCTGAATGT | 10477 |
rs562006556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037145 | ATCGTCAGACAGTGC[A/G]TTACTCACATGTTTG | 10477 |
rs562059310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015086 | AGAGTTGTTTTTTTC[G/T]TAATTAATATTTTTT | 10477 |
rs562062667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989562 | ACTCACAGTAGGCCT[A/G]GTTATTTCCTCCATA | 10477 |
rs562074760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014195 | AAAGATGGAAGTTTT[A/T]GTTTTTGTTTTCAAT | 10477 |
rs562249661 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043296 | TTACTAGTAGCATAT[A/C]AATTCAAGAGTAAGG | 10477 |
rs562250438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990790 | AAAATTCAGTTTGAC[A/G]TTGAATTACACACAG | 10477 |
rs562254571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983718 | TGTCTCATTTGCATA[C/T]AAGCTTGAAAAGAGA | 10477 |
rs562293308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027021 | ATTAGTAAAAAAATT[G/T]GTGCAGAGAATTGCG | 10477 |
rs562311779 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010291 | GTTACAGGGTTAATA[C/T]GTTACTATGATACTA | 10477 |
rs562337695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990409 | TTGCCTCTTGAATTT[C/T]TGAATAGTTTGCTTT | 10477 |
rs562398163 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986796 | CCTCAGGGAAGAAAT[A/G]TAAAGTATATCTGTG | 10477 |
rs562418947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006219 | GAGCTAGAATTGAGC[A/C]CAAATAGTACAGAAA | 10477 |
rs562471938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012028 | TGGAAGCATAGCTCC[A/G]CTTTGCTCTACTGCA | 10477 |
rs562516100 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063582 | CCTATTAAATGCATA[G/T]AGTTTTTTTCCTTTG | 10477 |
rs562518740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012940 | TGGACAAAGTCAGGC[C/G]TTGTCCACTCCCATA | 10477 |
rs562526876 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984963 | GAGTGGCTGCAAGGA[-/AT]TAGGCAGTTTTATGG | 10477 |
rs562545383 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998312 | ATCAACAATTACCCA[A/G]AGCAGAGATTCTGAT | 10477 |
rs562607427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982743 | CTGCTTACAGTTTTA[C/G]AAAACATGACTTTCA | 10477 |
rs562611724 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981213 | CGTGGCCGCCGCCGC[C/T]GGCCGTGGCTCGCCT | 10477 |
rs562640333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988037 | TTATTACCTTAGATA[C/T]ATTTTGGAATATTTC | 10477 |
rs562648664 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980066 | CTTCCTCCAGCTTAC[A/G]CGAGGGGCAAGTGGC | 10477 |
rs562692831 | in-del | -/CTCT | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988782 | GTACTTGGTTTTAAA[-/CTCT]CTCACACATGTAGAT | 10477 |
rs562767464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988695 | AAAGCTTTTTTCTAA[C/T]TGGCGTATGAAAGCA | 10477 |
rs562767477 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008692 | TGGAGGATTTCCTTA[A/G]TGGACTAGTTAAAGG | 10477 |
rs562787925 | in-del | -/GGC | 0.229136 | 0.249128 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980642 | GGAGGAGCCGAGCCG[-/GGC]GGCGGCGGCGGCGGG | 10477 |
rs562804186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990709 | AGCTTTAGGCTGGTT[A/G]TATCTATTATGTTCT | 10477 |
rs562822064 | in-del | -/ATTTTT | 0.00716266 | 0.059414 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983142 | TTTGACATTTTGTTA[-/ATTTTT]ATTGATAACTAAAGG | 10477 |
rs562838014 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020863 | GTAAATCTAGTGATA[C/T]GGTTGTAGGTGACTG | 10477 |
rs562845142 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030337 | TTTATTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 10477 |
rs562858140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041701 | TCAGCCTCCCAGAGT[C/G]CTGGGATTGATTACA | 10477 |
rs562859612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020650 | AATACTTCTTTGTTT[C/G]TTGTGTCTAAGTTCA | 10477 |
rs562875974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026843 | AACAGTTAATGATTG[A/C]TATTCAGGTCCAACT | 10477 |
rs562995196 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050095 | GTGAAGCTGGTAAGG[A/G]ATGGTTCAAAAACTT | 10477 |
rs563001277 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050188 | CTCTGATCACTATTT[A/C]CTGAACAGTTATTGA | 10477 |
rs563018603 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997402 | TTTCTTTTTTGTTTT[G/T]TATGCGCATGTTCTC | 10477 |
rs563076726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006726 | TGCTAAATTTGACAA[A/C]CCTCTCTGGGTCCTT | 10477 |
rs563077973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032219 | TATGAAGGCTAAAGC[A/G]AACATCATTATTTCA | 10477 |
rs563080428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039494 | GAGTGTACAGGGACT[A/G]GTGTGGTGGCTCACG | 10477 |
rs563086114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995719 | AGTTAGATCAAGAGG[C/T]TTGATCAAATTCAGG | 10477 |
rs563114884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034153 | AACTAGAAATACCAT[C/T]TGACCCACCAATCCC | 10477 |
rs563138848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036691 | CTCTTCAGCCACCCT[C/T]TACCCTGAACTGGAA | 10477 |
rs563140647 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031449 | TTACAATGTTTCAGT[A/G]GCATATATTTTTACC | 10477 |
rs563193431 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010406 | TAAGAGTAGTGGGTG[C/T]ACAAGTCGCGCTCTT | 10477 |
rs563281468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991257 | ATACATTTCAAGACT[C/T]CCTAGTGGATGCCTG | 10477 |
rs563289107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007940 | CCTTATCAAGGAAGG[C/T]TTCTACAGGAAAAGT | 10477 |
rs563321949 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994646 | ACCTTTGAACAGCAT[A/G]GATTTGAACGAGTGG | 10477 |
rs563352908 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014887 | GCTACTTTGAAATAT[A/T]TAATAAATTATTAAC | 10477 |
rs563373158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050234 | GAGTTACATACTAGT[A/G]TAGATTTTTAATGCA | 10477 |
rs563545742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009599 | TCTTTTTTGTTCAGA[C/T]AACCAAATATATTTC | 10477 |
rs563602426 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035168 | TTTAATATTTATATG[A/C]ATTCTATATAAGGGA | 10477 |
rs563804279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051031 | TCTTCGTACTTTCTT[C/T]CCAGTCTCATTCCTT | 10477 |
rs563835275 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008922 | TTTTTTTTTTTTTTT[A/T]ATCAGACTAGGGTAT | 10477 |
rs563877003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991569 | CGGCCCTTGGGCCAC[C/T]TGGTGGCCAGGATGT | 10477 |
rs563951040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013604 | AGGATGACATTTCCA[C/T]GTAACCTGGACTTCT | 10477 |
rs563967550 | in-del | -/CAGC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023577 | TTACTTTCTTTAACA[-/CAGC]CAGCCGCCTGATAGA | 10477 |
rs564079810 | in-del | -/ACTG | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038885 | GAAATACAACTACAT[-/ACTG]ACTAGAATGGTTAAA | 10477 |
rs564080253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982498 | GACTAACATTCTGAC[A/G]GATTGTTTAAGGAGT | 10477 |
rs564164943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043235 | ATGGTATGTTCTATT[C/T]TTTTACTAAATACTT | 10477 |
rs564174001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051002 | AGGAAATAAAACTAT[A/G]TATAGTTGAAGTTTC | 10477 |
rs564188646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049634 | GTAATAGTTTTGAAG[A/G]AAGACTATATGGTAA | 10477 |
rs564220952 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063473 | TGTTAGAAAGTGTGT[C/T]TGAGATGATTGTTGA | 10477 |
rs564270493 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035145 | TTACAGCAAAATAAC[-/TG]TTTTGTTTTAATATT | 10477 |
rs564329399 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983715 | TTTTGTCTCATTTGC[A/G]TATAAGCTTGAAAAG | 10477 |
rs564379669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020097 | TGGGAAGGTTGATGT[A/G]TTAGTTTCCTGGGGC | 10477 |
rs564384676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027829 | ATTGTACAGAAAAAA[A/G]TAAATTCTTTTACTA | 10477 |
rs564390673 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003038 | GTTGTTGGTATCTTA[C/T]GTAGTACATGTGTGC | 10477 |
rs564395304 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022415 | CTAGGGGAAATAAAA[G/T]ATTATCTTTTTTTGA | 10477 |
rs564414503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062555 | TTATAAAAGTCAAAT[C/G]TAACTTTTTATATAT | 10477 |
rs564469174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008767 | GTGCCTAAGTCAGGT[A/G]TGTATCCCACAAGCA | 10477 |
rs564516252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987015 | TGGCTTTATACATGT[C/T]TTAATATATTTTGAT | 10477 |
rs564578591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015266 | GGCCCAATATTTTAA[A/G]CCTACATATAGTCAC | 10477 |
rs564611579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057224 | ATAATACAAATTGTA[A/C]TTTAAAGAATTGTAT | 10477 |
rs564631567 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026979 | ATTTTACTAATCAGC[C/T]AGAAATATCTCTTCA | 10477 |
rs564640701 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045447 | AGAGCCCAGGCAATT[A/C]TGTCACATCTGAGGA | 10477 |
rs564650851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984677 | AACATTTTTAGTAAT[C/T]TTGGTGGTTGGAATA | 10477 |
rs564751899 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055224 | ATTGAGATGGAAACT[C/T]GAAGGGAGAGAGAAA | 10477 |
rs564794670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045508 | TTCCCCATTCTTTCT[C/G]CATATCTGCTCTCCC | 10477 |
rs564853971 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051499 | ATCTTAATTACCTAA[C/G]TCATTCCAGTCTTTT | 10477 |
rs564877328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023398 | CTGATTTCTCAAACA[A/G]TGTATATTGCCACAA | 10477 |
rs564878937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006668 | AATTATAGATTCATA[C/T]GTGGTTGTAAGAAAG | 10477 |
rs564940269 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029243 | AATGAGTCTTGATAT[A/C]TAGTAGGACAAGTAT | 10477 |
rs564962484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000103 | TTTGTTCTTGGCATT[G/T]AACCCAATTTCTAGA | 10477 |
rs565075455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004942 | GAAGGATTTTAAGTA[A/G]AACCCAAAACTTTTA | 10477 |
rs565097694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003884 | ATATTTCTGCATTCT[C/T]TCAGGAAGATGTTAC | 10477 |
rs565104476 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031964 | CGGCTCACAAATGCC[A/G]TTTTGGAAATGCCAT | 10477 |
rs565136429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004567 | GAAACATGGAGGCGG[A/T]GGTTGCAGTGAGCCG | 10477 |
rs565242943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008984 | TTAGTTGAATGAAAC[A/G]TCATTGGATCTTGAT | 10477 |
rs565261148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035588 | ATGATACATAGCAAG[C/T]TTGTTCAACCCATGA | 10477 |
rs565276167 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978711 | TGAGGTCATATGAAC[G/T]TCGTAGAATGAGGAT | 10477 |
rs565319153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015381 | TTTTAATACATCTAG[A/T]ACATTTTGTCAATAA | 10477 |
rs565332415 | in-del | -/TC | 0.00636936 | 0.0560724 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021478 | CTTTTTCTCTTTCTT[-/TC]TCTCTCTCTCTTCCT | 10477 |
rs565349172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010483 | TGATATTCTTAGCTG[C/T]AGAAGAAATCAGGGA | 10477 |
rs565399766 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046794 | CATAGAAATTACTCT[A/G]CCTACCTAAAATCCT | 10477 |
rs565463656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992511 | GAAGACCACTGTGGG[C/T]CCAGGGACTATCTTG | 10477 |
rs565531224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990935 | TGTTTCAGAATGCAG[A/G]AAGTTTCATGTTTTA | 10477 |
rs565567618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059921 | TTTTTTTTTCTCGGC[A/G]ACTCCAATTATGAAT | 10477 |
rs565572943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052448 | GCAGCAAAATAAGGC[A/G]GGTTGGACAAGTTTG | 10477 |
rs565589527 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021775 | CAGTGGATTTCTTAA[C/T]ACTTTTGCAGACTAG | 10477 |
rs565599536 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028125 | ACGGCATATATTGTT[A/T]AATTTTGAGCACTAT | 10477 |
rs565599610 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993760 | TTATTCAGGGTCCCG[A/G]AGAGAATCGATCTCA | 10477 |
rs565609475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984943 | AGATATGTGCTCAAT[A/T]ATGCGAGTGGCTGCA | 10477 |
rs565634482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057459 | TGGAGACTGGGTAAA[G/T]TTATACCAATTTTCT | 10477 |
rs565638479 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055111 | GTAATGGGAGGAAAT[-/G]CCTGTTGGGAATGAG | 10477 |
rs565693200 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995229 | GGCACTAGTGATGCT[A/G]GAAATGCTCCCAAGA | 10477 |
rs565712601 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014584 | GAGATTGGAAGAAAA[A/C]AAAGAGGTTGTATGT | 10477 |
rs565715524 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062512 | GCCAAAATTACAAAA[C/T]AGTTTTTGTATATTA | 10477 |
rs565730289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021123 | ATAATAGCTACAGCA[A/G]TATACCAGTCTTCGT | 10477 |
rs565779115 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034568 | GCATTAGGAGATACA[C/T]CTAATGTAAATGACA | 10477 |
rs565786420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027285 | TGGACCTCAACAAGT[G/T]TGGGAAAGTGTTATA | 10477 |
rs565801449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033518 | TCCTTACACCTTATA[C/T]AAAAATTAATTCAAG | 10477 |
rs565857569 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051361 | TATTTTAAACAATGC[G/T]AGGTTGGATATCTTC | 10477 |
rs565901036 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037449 | CGGTGGAAGACAGTA[G/T]TGATATATATGCTCC | 10477 |
rs565901769 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012266 | TACATGTACTAGTAT[A/G]TACTGTAAATTTTCA | 10477 |
rs565916430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033125 | TAATTTATAGATTCA[A/G]TGCCATCCCCATCAA | 10477 |
rs565940483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009019 | TAAATATTATAGCAG[C/T]GCTAAGGATACTTAT | 10477 |
rs565961104 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059115 | TTTGCTGAAATTGCA[A/G]TATATCATCTAATTC | 10477 |
rs566001943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015979 | AGCAATGAGAATGAG[A/T]CCAGAGTAATTAGCC | 10477 |
rs566070920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985891 | AAGTGCCCTCAGAGC[A/G]ATAGCCTAGTGTTGC | 10477 |
rs566072908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992397 | AAGTGCAATTAGACT[A/G]TAAAAGGAGATGTTA | 10477 |
rs566073729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998176 | TGACAAAAATATTAA[C/T]AGCATTTCCTTTCAC | 10477 |
rs566108336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044962 | TTAGAATTTAAAGTC[A/G]GAGAACTTACTAAGT | 10477 |
rs566109580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991944 | TGTGGTTGACCTAGA[A/G]TAGCTGGAACTGTGG | 10477 |
rs566160447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039312 | ATTTATACTTCAAAG[A/C]TGATTAAAAACATTT | 10477 |
rs566301014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059723 | GTATATGCTGTATTG[A/G]TCAGAGCAGTTCTAG | 10477 |
rs566358421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051070 | GGCCCAGAGGCAATA[A/T]CTATCCTGTATTTTT | 10477 |
rs566376395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040191 | CTTAGTGGATAAATG[A/G]AAGATTGCGTTATAG | 10477 |
rs566380468 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021179 | TGCGACTACGAAACA[A/T]GAGATTAGTCAGGAT | 10477 |
rs566406058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050602 | TACATTTTATTTTTG[G/T]CAGGAGCTGGGTAAT | 10477 |
rs566417864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058234 | AATAATGTGAATTTT[A/G]TGCTGAATACCTTTA | 10477 |
rs566449441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029369 | ATTTTATTGAATTTG[A/G]GAAATTAGAAGTAGA | 10477 |
rs566466092 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007611 | TTTGACCTTCCATTG[G/T]TTGAACTTTGGTCTC | 10477 |
rs566470631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005068 | TTATTTGGTTGCAGC[A/G]GCATACAACTCAAAC | 10477 |
rs566482196 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011096 | TGACTTTTTTTTTTT[A/T]AATTAGTTAGAGCCA | 10477 |
rs566486156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004663 | GCGTTAAGTAACTTT[C/T]GATTTGGGACTAAAT | 10477 |
rs566595604 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980318 | AAGCCACCCCGCGGC[A/T]CAGCGGCCCCGCGAT | 10477 |
rs566646034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017524 | CCAAGGGAAGACAGC[A/G]TGTATGTGTATTGTC | 10477 |
rs566685133 | snp | A/C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024287 | ACTTAAAGTGAGCTA[A/C/T]GAATTAATGTTAAAA | 10477 |
rs566724507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061942 | ACAACCTCAATGCCC[A/G]TTAATAGATGTAACG | 10477 |
rs566725085 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035662 | CAAATTCGAAAACTT[-/C]CTTGAAACATTATTA | 10477 |
rs566745592 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042890 | TTTGCACAACGTCAC[A/G]CATCTGGTAAATGCA | 10477 |
rs566779089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986489 | TTGTATTGTATTTTT[G/T]CCTTCATGTCAGATC | 10477 |
rs566836587 | snp | A/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181043899 | ATTGATTGAAAACCG[A/T]AAGTGATTTAACCGT | 10477 |
rs566914796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025351 | CCACTATGCAAATAA[A/G]TGTAATTTTCACAGT | 10477 |
rs566928292 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985491 | ATAAAATGTTAAAAT[C/T]AATTTCACTTTTTTA | 10477 |
rs566943413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994251 | ACTTTTCCCTTCTGC[C/G]GAGGTTTCTTAATTT | 10477 |
rs566970846 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991801 | TATGGATAAACTGGA[C/T]AAAAGTATGATTCAA | 10477 |
rs566974746 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026177 | CACTGAAACCCTTTG[A/G]AGGATTAAGTTAAAT | 10477 |
rs567031538 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005398 | ATATGGTTCATGCCT[A/C]GGCCACTGCTCTATC | 10477 |
rs567115939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045894 | GAAAAAAAAAAGACA[A/G]CAATCAATTTGTTAA | 10477 |
rs567154408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010070 | ACATGCAGTTTTTAC[C/T]CATTCTTGATTGCAG | 10477 |
rs567166200 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987616 | TGACTAGCAAAACCT[C/G]AGATCAGGTGATTTC | 10477 |
rs567188112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034993 | GAAAGACAACTAATA[C/T]TTTAGGTGATTCTAT | 10477 |
rs567227602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052010 | CTGAGGTATTTCCAT[A/G]TAGTTTGGCACAATG | 10477 |
rs567243875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010536 | TTATAGATTCTGCCT[A/G]TCCTCCTGAATCTGT | 10477 |
rs567271337 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021855 | GAAAATACTTCTGGG[-/T]TTTGCTTTCTTAAGT | 10477 |
rs567336447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016697 | AACAACTGTCGCCCT[A/G]TCAGTCTCACGACTA | 10477 |
rs567405792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058461 | TGCAAAGCTTAAATA[C/T]AACAATTACTTGAAT | 10477 |
rs567419346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985739 | ATGAAAAATGTAAAG[A/G]TCTATCAATTCAGAA | 10477 |
rs567440384 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986242 | GTTTATGTGTGGCTG[G/T]GGTATGTGAAAAACA | 10477 |
rs567446856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023506 | GCTACTTAAAGGAAT[C/G]ATGAATTGCTTTGTG | 10477 |
rs567458117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991855 | ATGTGAGATTTCATC[A/G]TGCTACTTAGAATGA | 10477 |
rs567492943 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029327 | TATCAAATTCCTTGG[A/C]AAAGTATTCTTGTGG | 10477 |
rs567514815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022805 | AGTGCTGCCTTGTTC[A/C]ACCTCAGCTGGGACT | 10477 |
rs567537098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999395 | ATAGTGTTGCTGTGA[A/G]GGATTCACAAATACA | 10477 |
rs567615508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023997 | AATACCTGTGTTTTA[C/T]ATTTCTTTTGCATTT | 10477 |
rs567623763 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979081 | AATCAAAATGCTTGT[C/G]CACACACAGACCATG | 10477 |
rs567628577 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991346 | TACGTTTACATAAGG[G/T]TTACAAATTAGGCAC | 10477 |
rs567661738 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050444 | TAAAGTTTGGGAGGG[A/G]CTCTTAGAGTAGACA | 10477 |
rs567664495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987433 | CTAATTTCTTTCCAT[A/G]TAGGAAGAAGCACAA | 10477 |
rs567676950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030101 | CCTCCCAAAGTGCTG[C/T]GATTACAGGTGTGAG | 10477 |
rs567725585 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046417 | GGACAAACAGGTGCT[G/T]TTAGAGTCTGTGTTT | 10477 |
rs567753743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036352 | TAGAATAACTGAGTA[C/T]CTATACACAAAATAC | 10477 |
rs567786223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035234 | GTAAAACCTACACCT[A/G]TTATACTATGATTTG | 10477 |
rs567813441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035841 | AGAGGAAGGTCACAT[A/G]ATAGGTAATATAAGC | 10477 |
rs567894048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034920 | TGAAGAATATGAAAT[A/G]CTAACATTAGGGAAG | 10477 |
rs567923059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012105 | TGTTTTCTTTTGAGA[A/G]AGGGCAATATGATCA | 10477 |
rs567950459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046289 | GGATTCCGTGTAGGC[A/G]TTAAGGTTCTGAACA | 10477 |
rs567971131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039467 | TGGTCGAATGTAAAA[A/T]CATTGTCTTAAGAGT | 10477 |
rs567979232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004601 | TTGTGCCACCGCACC[C/T]CAGTCTGGCGAAGAG | 10477 |
rs567984721 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011328 | GTGATGGGGAGAAAA[C/T]GGGGGTGATAAGGAG | 10477 |
rs567986465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018776 | TATAATAATAAATAT[A/G]TATAATTATTTTCTT | 10477 |
rs568000426 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031133 | CTCATACTATTTTTT[A/T]AAAAAATTTGTTAAA | 10477 |
rs568028852 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012394 | TCTAGATAGTTTGCT[A/G]TGTATTTTAGGTACT | 10477 |
rs568057997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995202 | TAACACCATGGGACC[C/T]ATGGTGTTAGTGGCA | 10477 |
rs568058097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989214 | TAGTTTCTTCAACAC[A/G]ACTGTAATAAAGTAC | 10477 |
rs568094839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994676 | GGTTCATTTATACAC[A/G]ACTTTTTTCAATAAA | 10477 |
rs568166182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015438 | GGATAGATGATAGTA[C/T]TTAATGATTTTTGCA | 10477 |
rs568168792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005199 | CCATTTGCTTGCTTT[A/C]CTTCCTCTTAGTTGA | 10477 |
rs568177947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000787 | TCTCGATCTCCTGAT[C/T]GTGTGATCCGACCAC | 10477 |
rs568212259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047874 | AGCTGCCTATTTCTT[C/T]TAATATAAAGACAAG | 10477 |
rs568242798 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047376 | GACCTGTGTATCAAG[G/T]TCTCACAAATTTATA | 10477 |
rs568282679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021413 | TTTCTTTTCCCCTCC[C/T]TCCCTCCCTTCCTCC | 10477 |
rs568287214 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995515 | ATTAAGTTTTTGGGG[G/T]CATCAGAAGTTATAC | 10477 |
rs568305924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053583 | TTCATAGCAAAATTG[A/G]GTGAAAACCCCTTGT | 10477 |
rs568323638 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054246 | TCTTATGGTAAGATA[A/C/T]GTTTATGTTTGTAAC | 10477 |
rs568329834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049836 | TAGCACGCACACCCA[C/G]CCATTTTATTTTTAT | 10477 |
rs568332441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062173 | AGTCAGGAAGGAAGA[C/T]AGTTTTTTTTTACTG | 10477 |
rs568388011 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030944 | CACTATTTTGTGTTT[A/G]TGTTGTGTTTCACTA | 10477 |
rs568407236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060994 | AAGTAGACTAGGCCA[A/G]AAGTTTCTCAATACC | 10477 |
rs568538054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013713 | TGTATATGTGTGCAG[C/T]AGATGAAATCCTCAT | 10477 |
rs568539302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041337 | ATAGGGGCATTGAAC[A/T]GTAATAGAAGCTTAG | 10477 |
rs568544819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982896 | GCATTGTCCTTGGGC[C/T]TCTTCACTCTGAAAC | 10477 |
rs568609748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026463 | GAAGGTAGAGCAGAG[A/T]CACCTCTGTGTATTG | 10477 |
rs568609965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047757 | CACCCACAGCCCCTC[C/T]GGGCCTCCTCCAGAC | 10477 |
rs568650700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013232 | TATTGCTACTTAACA[A/C]ATTACCCCACAATTT | 10477 |
rs568708278 | snp | A/G | 1.66774e-05 | 0.00288763 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982075 | AAGGTCCGATGATGA[A/G]AGCCCCAGCACCAGC | 10477 |
rs568740665 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982329 | TCAATAGCAGTAGTT[A/C/G]AGAAATATTTACTTC | 10477 |
rs568760651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031702 | TTTTGTTTTGTTTTG[C/T]TCATAATTCCATTCC | 10477 |
rs568776706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989874 | AGATGGATATGTTTA[C/T]TTTTCAGGAAAATCA | 10477 |
rs568802852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004803 | AAAAGTAATATATAT[A/G]TACGTAGTAGGTGAC | 10477 |
rs568807525 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004258 | CAGTGTGTAGTAGTT[A/C]TAGTTGTAAAACTTG | 10477 |
rs568821813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000715 | GCCCACCACCACACC[G/T]GACTAATTTTTTGTA | 10477 |
rs568846084 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036951 | CCAAGAACCTATCCA[C/G]AACATTAAGCGAAGA | 10477 |
rs568958654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010596 | TTTCACAGGTAGATA[A/T]AAAAGGAAAATAGTA | 10477 |
rs569009099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053477 | ATTACTTACAGAAAC[A/G]TTGACCTCTTATTTT | 10477 |
rs569093954 | snp | C/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980415 | CCGGGTCCCCGCCGC[C/G]CTCTTTGTCCTGGCC | 10477 |
rs569130502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055546 | CTACCTGGATTTTAG[A/G]ACTGGATTTTAGCCT | 10477 |
rs569174832 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978915 | TTAACGTACAGCTTT[C/T]CTTTTCTGTCTCCCC | 10477 |
rs569227752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006544 | ACATGGAGCACACTT[A/T]TATGCATGTTAAATA | 10477 |
rs569242278 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028547 | TCTCTTTGCGCTGCA[C/G]GTTTATCAACTCTGA | 10477 |
rs569263470 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046616 | AGTTTTGGATGAGCC[C/G]TTAAACTGTACAGTG | 10477 |
rs569289355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021061 | CTTACCCTACTATAT[A/G]TGAAAAGTAGTAATT | 10477 |
rs569305974 | snp | A/T | 0.416871 | 0.186156 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061114 | CAGACCACTTCTTTT[A/T]TTTTTTTTTTTTTTT | 10477 |
rs569341932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019621 | AACACAATGTACCAG[A/T]GATTTTTTTAAAAAG | 10477 |
rs569365621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026662 | TAAATATTTGACTCC[A/G]GCCCTTTCGTGTATG | 10477 |
rs569370325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005276 | TAGTACCTCCCAGCT[A/G]TGTTCTTCAGATTGA | 10477 |
rs569402488 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011720 | ACAATTTAATCATTC[A/G]GGTCCTCTGGCAAGT | 10477 |
rs569414305 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989789 | CAGCTACATGCTCAC[A/G]TAACCAGTCATATTC | 10477 |
rs569423864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996716 | TTCCACATTGTAGTG[A/G]TAGCAAATCATAATG | 10477 |
rs569453892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018912 | TGCTCTCAGATTTTT[C/T]ATTGTAAAGTAAGGA | 10477 |
rs569484858 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009481 | CCACATACTACTACT[A/C]CTACCATAATGGTGT | 10477 |
rs569485440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031046 | AGATTGGGTTCTTAA[C/T]TTTTAGCTTTTCTTC | 10477 |
rs569508876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989092 | CATTTTGGCATCAGC[A/G]TAAACCTCAAAAATC | 10477 |
rs569511773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025418 | ATTTTTTCCCTGACA[C/G]TTTATGTTAAAATAC | 10477 |
rs569512511 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996070 | CCCATTGTAGTACTT[A/C]AGTATATTGCTGTTA | 10477 |
rs569515971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006891 | TAAAATTACTTAAAC[A/G]TTTTCAATTTCTCAG | 10477 |
rs569603437 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032971 | GGAATCCAACTTACA[A/G]GGGATATGAAGGACC | 10477 |
rs569619325 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012027 | GTGGAAGCATAGCTC[C/T]GCTTTGCTCTACTGC | 10477 |
rs569706377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983049 | CAATGAGACTCTTAT[C/T]AGTGGTAGTAGTAGT | 10477 |
rs569726518 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998802 | CAGATACGTTTTTAT[C/T]CAAAAAGGAGTAAAA | 10477 |
rs569736337 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034921 | GAAGAATATGAAATA[C/G]TAACATTAGGGAAGA | 10477 |
rs569743090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990483 | CACCTACACCTTCCT[C/T]AGCTGATTCTTCACT | 10477 |
rs569796834 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026566 | CAAAGGCTGAGGAAA[C/G]AGAAAGTGAGAGAGG | 10477 |
rs569801985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044757 | GTGAATGGTTCTTAC[A/G]TTAATCACTATGTTA | 10477 |
rs569816000 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044170 | ACAATTTCTGGTCTT[C/T]GGTAGGGCCAGGTTT | 10477 |
rs569859373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036928 | CATTTCACATAAAGT[A/T]GCAGTTTCCAAGAAC | 10477 |
rs569978973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049131 | TTTATGTCACCATTA[A/G]CAGAGAAGTCAAGGA | 10477 |
rs570018862 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998093 | AGTTCTGAAACTTGC[C/G]AGACTCAAAGTGTAG | 10477 |
rs570027711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991368 | ATTAGGCACAGCAAG[A/G]GATTAACAACTTCCC | 10477 |
rs570049372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003519 | ATTACAGTTGGACTT[C/T]ATTTGATATAAATTA | 10477 |
rs570068634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033828 | AGAACTCAAACAAAT[G/T]TAGAAGAAAAAAACA | 10477 |
rs570112963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050410 | TTGTTCAACGGGATT[C/G]TCTTCAGAAATATAA | 10477 |
rs570143507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008139 | GACATTATGGGATCT[C/G]TGCGGTATAGACAAA | 10477 |
rs570154021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032370 | ATCTGATAAAAAATA[C/T]ATATTATCCTTTTAT | 10477 |
rs570159128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015298 | TTAGGACATTTTAAA[A/G]TGAGGGCTTTATCAC | 10477 |
rs570165728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031792 | CTTTACTGTGCTTAC[G/T]TAAAAAGAAGTCGTA | 10477 |
rs570307049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050151 | ATTTTAGGAAAAGAA[G/T]CCACTTCTTTACAAG | 10477 |
rs570322074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006350 | CTCCCTGTTCAATGT[A/C]TATGCATTCTGTTCA | 10477 |
rs570324814 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035691 | AGATTTTTTTTGCAA[-/T]TTTTTTTTAAGCTCA | 10477 |
rs570380734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995934 | ACCTGGTCATACATG[G/T]TAAAGGTAAGATATG | 10477 |
rs570541590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995329 | GCAGCTGTAGGTGCC[A/T]GCCATTTCAGACAAG | 10477 |
rs570545657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036449 | CTGATTCCTGGCAGG[A/G]GCCATTGTGTGGAGT | 10477 |
rs570681378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056648 | CTTCCCAACATTGCC[A/G]CGTTTGGGGGTCAGA | 10477 |
rs570704189 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999792 | GCTTGAGCAAGTTAT[C/T]TCCTCTGATTCTCAG | 10477 |
rs570755056 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048316 | AGATTCCTAGCCCCA[A/C]ATCGTAGACACTCAA | 10477 |
rs570768614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027096 | GTTCTTAATAATCTT[C/T]ATTAAAAACTTAGTT | 10477 |
rs570775268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996990 | CACACATGGCTCTTA[C/T]AAATATGTGACTCTG | 10477 |
rs570795249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055722 | TACACTTTGTCCGAT[A/G]GCAAATAGCATGATA | 10477 |
rs570819592 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982759 | AAAACATGACTTTCA[A/G]TCGTATATCACAGGT | 10477 |
rs570857181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002886 | CACCCCAGTTTGTGA[A/G]AAGATGGACAACCTT | 10477 |
rs570869101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008083 | GTATTGAGATTTAAT[C/G]AGTTTAAAGTTGGGC | 10477 |
rs570920056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043617 | TTAACCTGAATTATT[G/T]TATAATATTTGATAA | 10477 |
rs570924835 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019798 | GCTAGTTAACGTAGC[C/T]TTCACCTTACATACT | 10477 |
rs570941958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014333 | ACATTTCATTCTGAT[A/G]CAACTCAGAGAAGCA | 10477 |
rs571038109 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063751 | AATGTCTTATGGAAC[A/G]TGTTGCTTCCAAATT | 10477 |
rs571070233 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046914 | CTCTTATTTTTCAAA[A/T]TAAAAATTACACAGA | 10477 |
rs571090204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020298 | TACCTCCATTGTCAC[A/G]TGGCTGCCTTCTTCC | 10477 |
rs571127600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983983 | AGAGGGCAGTGTAAT[G/T]CCCTGGTTATTCTGT | 10477 |
rs571197153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058912 | TGGTCCCATCAGCAT[A/G]TAAGATCTTGAAATT | 10477 |
rs571288197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023961 | CCTACTCCTTACTGT[C/T]ACAAGTGATAAAGCA | 10477 |
rs571349596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029991 | GGCGCCCGCCACCAT[A/G]CCTGGCTAATTTTTG | 10477 |
rs571357980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029503 | AAGTATTGTACATCT[G/T]TTGCTAAATTTATTT | 10477 |
rs571377786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991334 | ACATACCTATGATAC[A/G]TTTACATAAGGGTTA | 10477 |
rs571409499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991783 | GGACTAGAGCATATA[C/T]AGTATGGATAAACTG | 10477 |
rs571444582 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999335 | TAGTTTATCTCCTCA[C/G]CAGTTGTGAGCCTTT | 10477 |
rs571445334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028692 | TCCATTCTCATTTCT[A/G]TGAAATGCCTTTTTT | 10477 |
rs571450420 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028790 | CCTTTTGTACATATA[A/T]GTTGCAAAAATCTTC | 10477 |
rs571462241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034254 | GTGGCAGTATTCACA[A/G]TAGCAAAGACTTGGA | 10477 |
rs571464625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997479 | CTCCCACTCTCCTTA[A/G]TATTTAGTATTTCTT | 10477 |
rs571468558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038006 | TAAGCTAAAGTTAAT[G/T]TATTATTGTGGAAGA | 10477 |
rs571509387 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049223 | ACAATGAATGTGAAT[A/G]TAAAAAACAAGGGAT | 10477 |
rs571520772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033687 | AGACAAATGGGATCT[A/C]ATTAAACTAAAGAGC | 10477 |
rs571587513 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005929 | TTGAACTGCTTCTGG[C/T]AATTTCTTAGAAGAG | 10477 |
rs571603756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987273 | ATTTGTATTTATTGA[A/G]AATTGTTGACTAGAA | 10477 |
rs571650684 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030708 | TTTTGTATTTGGGAT[A/T]AGGTGGGGAAAAGGT | 10477 |
rs571664354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034600 | GTTAATGGGTGCAGC[A/G]CACCAACATGGCACA | 10477 |
rs571693798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007778 | GGAGAACTTTCCACA[A/G]TGGTAGAAGGGCTTG | 10477 |
rs571729782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039758 | CGTAAAATGTCATCC[C/T]GTGGTATCCTTGGGG | 10477 |
rs571731246 | in-del | -/TTAG | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026617 | GGGATTATCTGGAGA[-/TTAG]TTAAAGTTTCACTAA | 10477 |
rs571755863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007276 | GCCTAATTAAAATAG[C/G]TTGCTACCTTATCCT | 10477 |
rs571757708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014635 | AGTATTTCATAGGTG[G/T]GCCAGGTAAGTTGAG | 10477 |
rs571807070 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990742 | TAGGAGTACTAAAGT[A/T]ACATCATGGAGAAAT | 10477 |
rs571873388 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018603 | AATTTCTGTGTTTTT[-/TT]TTTTTTTTTTTTTCC | 10477 |
rs571935629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009980 | GTGTATTTGTATTTT[A/G]ATATTTTAAATACTA | 10477 |
rs571968279 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007745 | GCTGCAGGTTTCTGT[C/G]TACACTAGTGCTGGA | 10477 |
rs571974758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043220 | TTTTTCATTGTATCC[A/G]TGGTATGTTCTATTT | 10477 |
rs571979789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045218 | GTTTTCTCATTTGAT[C/G]AATTTTAAAAAGCTG | 10477 |
rs571993012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002143 | GTAGGGATGAGGTTG[A/G]CTTTATGGCTGGCCT | 10477 |
rs572044432 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009932 | TTTTCCAGTTTTTTA[A/G]TACTTTTTTTACTCT | 10477 |
rs572070913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020503 | CCTACAATTCAAGCT[C/G]TCACAGTTGATTAAA | 10477 |
rs572089288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049557 | ATACACAATAGACTT[C/G]ACTGCGTTTGGATGA | 10477 |
rs572126157 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054052 | TAGCACCGAATAATA[C/T]TTCGTTGTCTGGAGG | 10477 |
rs572175283 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059249 | AATTATTTCTCTGCA[A/G]TGCTAAATCTTTTTG | 10477 |
rs572221061 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036375 | CAAAATACAGCAGGT[C/T]CTTGAATAATGGTTC | 10477 |
rs572240680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020063 | TGAGTTTGACTACTG[C/T]ATTTCTTATCTGTTT | 10477 |
rs572300171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026293 | CATATTCTGTAGATT[A/G]TCATGGCATTTTTTT | 10477 |
rs572307180 | snp | A/G | 0.000167258 | 0.00914335 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057854 | AGTGCATTCTTTAGT[A/G]TTTAATCCTTCTCCT | 10477 |
rs572331811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027805 | TAACTCTACTTTCCT[A/G]GTCATTTGATTGTAC | 10477 |
rs572379388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032043 | TCAGGGAGGTGCTCC[A/G]TTAGGAAAATCTAGA | 10477 |
rs572382370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022345 | ATTATTCTCGGTGGT[A/G]TTATGTTCCATAAAG | 10477 |
rs572398383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037578 | GCTTATAGACAAATA[A/C]AAAGGAAAATATTTT | 10477 |
rs572586207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984608 | GTGGTCGTTTTCTAC[A/G]GAATGCATTGTTGGA | 10477 |
rs572596090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997628 | TCCTAGTGGTTGTCT[A/G]TCAAAAGTACCTGCA | 10477 |
rs572623742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991123 | CTACCAAATTATTTT[G/T]TAACAACCTTATTAA | 10477 |
rs572785334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051461 | TTACTGACCTACAAA[C/T]GTTTGTAATGAACTG | 10477 |
rs572825232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998520 | TGCTATGGAAGAACA[A/G]TTAAGATCATGTTTC | 10477 |
rs572846842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050900 | TTTGAAACTTCCTTC[C/T]TTCTTGTTTCAACGT | 10477 |
rs572886328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039536 | AGCACTTTGGGATTT[C/T]GAGGTGGGCAGATTG | 10477 |
rs572887788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005250 | TCTCCTTGTGATCAT[A/G]AGATAACTGATAGTA | 10477 |
rs572907387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034660 | GTGCACATGTACCCT[A/G]GAACTTAAAGTATAA | 10477 |
rs572921140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045354 | AATAAATTCACCACA[A/G]TCTAAAGATGTTAAT | 10477 |
rs572938657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994056 | ATGGAATTCAATGGC[A/G]GTTTTAACTAGTGTG | 10477 |
rs572950786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011570 | ATCAAAACTAAGTCA[A/G]AAATTTTTTAAGAAA | 10477 |
rs572965580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010723 | CCTGTGACTGATACA[A/G]TCAATTTAGGGGCAA | 10477 |
rs572979409 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036870 | GGAACTTAAATCTTG[-/T]TTATGTCAATTAGCC | 10477 |
rs572999030 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006292 | AGGCCATAGAGTTTG[C/T]TTAAATAGACATACT | 10477 |
rs573120628 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000741 | TTGTATTTTTAGTAG[A/G]GATGGGGTTTCACCG | 10477 |
rs573120840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040614 | TAATTTCTATTTAGT[A/G]TAAGGTATACTACAA | 10477 |
rs573122217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009322 | AACCAACTTTGAATT[A/G]CTAAATTATCTTACC | 10477 |
rs573134707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008639 | AGAGAGAGGAATTAG[A/G]CCTGGCTGTGGCGGA | 10477 |
rs573216546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986944 | ATTAGTATATAGTTA[C/T]GTCTAGTACATACAT | 10477 |
rs573216556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993089 | GGGATTTTTATCTCT[G/T]TTGACATTCTATCAG | 10477 |
rs573257454 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045139 | CTGTCATAATCTACT[C/T]TTTAAAGACAAATGT | 10477 |
rs573289528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002465 | GGAATGATTACGAAC[A/G]AAGAAAACCCTCTAA | 10477 |
rs573319432 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042946 | TTCCAAGCCTTTTCA[A/G]TACAGTTTACTGCTT | 10477 |
rs573363049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017703 | ATTTAACAACAGCAT[A/G]AAAGGTTTTTTTGTT | 10477 |
rs573373217 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979153 | GTGGAATATCCTTAC[C/T]ACTTATGAACCTAGC | 10477 |
rs573381962 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978638 | GAGCAGGAGAGGACT[C/T]AGAACCTTTGATACA | 10477 |
rs573398172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017256 | TGGGATACAGTGGTC[A/C]AGACTCCTGGAAATA | 10477 |
rs573412427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023778 | TTAATTTTTAAATGA[C/T]GATGATAAAATATCT | 10477 |
rs573422309 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983135 | AACCAATTTTGACAT[C/T]TTGTTAATTTTTATT | 10477 |
rs573423554 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053080 | CTCGTTCTTTGTGAC[C/G]AGAATTTCCTTATTT | 10477 |
rs573436161 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059904 | TCAAATGATCAGAAA[A/T]TTTTTTTTTTCTCGG | 10477 |
rs573447711 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042367 | CTCTTCTGGTTAGCC[C/T]CCCATCAGTGTGACC | 10477 |
rs573500914 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059498 | AATAGCCACATAAAA[C/G]ATAAAACAATTTTAA | 10477 |
rs573531944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030172 | TGGTTGTCTTTGGTG[A/G]TGGTGGTGGTGGCCT | 10477 |
rs573599138 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012745 | TGTAATTACAATCTA[G/T]GTTTTGAATTATGGT | 10477 |
rs573624571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003207 | TATTAGCCTAAATAT[A/G]TTTTCATTGGTGTTC | 10477 |
rs573709686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050744 | CGGTTTCTCATCTGT[C/G]AAATTGTGATAAAAA | 10477 |
rs573719274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051226 | CAGCTTAACTTTTTT[C/T]ACTCAGCATTATTTT | 10477 |
rs573738368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008529 | TCTGGCTGAGGTCCA[A/G]CTGGATATATACAGC | 10477 |
rs573772496 | snp | A/C/G | 3.30569e-05 | 0.00406541 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181057759 | TCCACCGGGTTCTGT[A/C/G]TATGAAGGTGGTGTG | 10477 |
rs573820976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044415 | GCAAGAAGGATGCCA[A/C]ATATCACTTCAGGGC | 10477 |
rs573903357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028269 | TTTCATGCTGTATAC[A/G]ATTTTATTACGTGGA | 10477 |
rs573929057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992574 | GTATCTTGTAGCTCT[A/G]ACATTTGGAACATAT | 10477 |
rs573931772 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007449 | GAGTAGACTGGACTC[C/T]GGAAAAGAAGAGAAA | 10477 |
rs573934435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004462 | GCATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10477 |
rs573966431 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031743 | CCATTTTTGGAGGCT[A/G]TACACTATTTCTGTA | 10477 |
rs574053345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060513 | TCAACTGAGTCAAAA[A/G]CATTTAATTTTGTTA | 10477 |
rs574067022 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049965 | TATTTATTTGCCATA[C/G]CCTGAATATATGAAA | 10477 |
rs574102707 | in-del | -/TTAC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053463 | TCTTTTTATAAACCA[-/TTAC]TTACAGAAACATTGA | 10477 |
rs574185365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986026 | TTCACTTGTCTTTCT[C/G]TTTATATACCAGATT | 10477 |
rs574213153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029551 | TTGATGCTTTTGTAA[C/G]TTTTATCTAAAAACT | 10477 |
rs574213919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059415 | ATCTGAACATAAATT[A/C]TTTCTATATTCTAGA | 10477 |
rs574240148 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031147 | TTAAAAAATTTGTTA[A/G]AAATTGCTTTTGGAC | 10477 |
rs574262751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034476 | GGTGGGAATTGAACA[A/G]TGAGAACACTTGGAC | 10477 |
rs574272183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034642 | GTAACGAACCTGCAC[A/G]TTGTGCACATGTACC | 10477 |
rs574359411 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010811 | TGTCATATCCTCCTC[-/T]TTTTTTTTTTTTTTA | 10477 |
rs574365114 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979882 | TTTTAAGAATGTTGA[A/G]CGGGACATTTTAAAC | 10477 |
rs574405547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024847 | TTTTTTTTTAACTTA[A/G]GTAATATTGCTTGAA | 10477 |
rs574447536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995532 | ATCAGAAGTTATACT[C/G]AGGTTTTTTCCTTTT | 10477 |
rs574465809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987848 | GACTGTCAGCATCTG[C/T]GTCACAGATGAGGTT | 10477 |
rs574515806 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010211 | TTTATATTATTAATT[-/GTG]GTTCTCTATAGTTCT | 10477 |
rs574584500 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016595 | ATAAGTAATGGAGGT[A/G]GAATCCCAGCTCAAG | 10477 |
rs574660057 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056376 | TAGGTTATAAGGAAA[A/C]GAGGTTTATTTGGTT | 10477 |
rs574748831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001466 | GAATGTAGAGGGTGG[A/G]ACATCAAGAAGTGGA | 10477 |
rs574809128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006584 | TGCTAAATATTTCTC[A/G]TTTAGCTGAAATTCA | 10477 |
rs574821066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042454 | TTTTGGAATTAGGGA[A/G]GTCCTTCTATTTATT | 10477 |
rs574894298 | in-del | -/AAAAAAC | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022726 | TAAGTAGGCTGCAAA[-/AAAAAAC]AAAAAACAAAAAAAA | 10477 |
rs574931859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047993 | TTCCCTTCTGCCACA[C/T]TGTGCTTCCAGGCCC | 10477 |
rs574968895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036004 | CAAACAGTAAAGTCA[A/G]TCCTGATTTCTTGAG | 10477 |
rs575075741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053983 | TCTCCCACTTACTAA[C/T]ATGCATTTAAGTTTC | 10477 |
rs575147818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011736 | GGTCCTCTGGCAAGT[A/G]GTGTTATAGAAATTG | 10477 |
rs575193111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052118 | GAGTGAATCTTATCT[A/G]GTTGTTAAGGTTGAG | 10477 |
rs575298509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040267 | GATACATCCTTCTTC[A/G]TCCTTCCACGGGACA | 10477 |
rs575339870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030221 | GGCATTAAATTTTAA[A/T]GAATACTTTATCTAC | 10477 |
rs575439435 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999653 | CCTCCCAAAAAAAAA[A/G]AAAACCAAAATATAA | 10477 |
rs575519383 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983240 | TTCTATGGATTTTCA[C/T]CCTTATTGTCTCAGT | 10477 |
rs575545757 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979220 | CTCTTAGCACAGAGT[A/G]GAGACCTGGCTTTAG | 10477 |
rs575672880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020388 | ACCATACTCTGGTAT[A/G]ACCTCATCTTCACTA | 10477 |
rs575683419 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992486 | TAAAGATTTATTTCT[-/CA]CACTCATGTGAAGAC | 10477 |
rs575685436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019887 | TCTCAGCAAATATCA[A/C]GTGTATGATACAATA | 10477 |
rs575686594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054417 | GTTGTTGGTGTTTTG[G/T]ATTTGGGCCATTCTA | 10477 |
rs575728964 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006399 | ATTTTTGTTGCCTTC[C/T]ACCTTTTGCCGTTCC | 10477 |
rs575744070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053898 | CTGATATTTTTACTG[C/T]TTCTGTAGTTTTGCC | 10477 |
rs575747214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026241 | TATTCTCATAGAAAC[A/G]GAAAAACCAGTTGTT | 10477 |
rs575750787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984947 | ATGTGCTCAATAATG[C/T]GAGTGGCTGCAAGGA | 10477 |
rs575775229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011615 | TGCACAGGAACGATG[A/G]TATAGAAGTGCCATT | 10477 |
rs575783226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047960 | ATTAGGTCGTTTCAT[A/T]GTACTTCCCATGTTC | 10477 |
rs575810493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060484 | CTATACAGGGTAAAA[A/G]CAAAAAATTTTTTTC | 10477 |
rs575837211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018454 | AGGATTGTACAGTTT[A/G]TCTGGGTGCAGATAC | 10477 |
rs575846380 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047518 | AACATCCATATCTTA[G/T]TTAATGGCATATACA | 10477 |
rs575866884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025579 | AAATACCACATATTA[A/C]TTTTTTTTCTACATT | 10477 |
rs575866929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995460 | ATGTAACATACAAAA[C/T]GTTTCTGTTATTGGT | 10477 |
rs575927349 | in-del | -/TA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025398 | TGTCATTGAAGATAT[-/TA]TCTATTTTTTCCCTG | 10477 |
rs576002685 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055303 | GATTCTTATTGGCAT[C/G]ACTCACCAGAGAAGG | 10477 |
rs576008693 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047574 | ACTATAAGCTATTCT[C/T]GAAACCCTCCTTTTC | 10477 |
rs576021812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024091 | TGTCGTTGTAGGTCA[G/T]GTAAACATGTATGTT | 10477 |
rs576044657 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001617 | GGAGCCTGAAATGGC[C/T]TAAGAGCCCTGTCAA | 10477 |
rs576168504 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028518 | ACACATTTCCACCAG[A/C]AAAGTGCAATAGTTC | 10477 |
rs576193547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043668 | AAATATAATAATTAA[C/T]GATAATCACCATAGA | 10477 |
rs576219292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989373 | GTTAATAAATAAATT[G/T]AAGTCTCTCAAATTG | 10477 |
rs576231073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062330 | GTAAGTTTTCAAGTG[C/T]AAATATTGATAGTGA | 10477 |
rs576283820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031385 | ATATTGCTGTATAAT[C/G]TTTGCTGTATTACTA | 10477 |
rs576297899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035954 | TATAAAGTAAGCCTC[C/T]AATGTGGTAAGTGAT | 10477 |
rs576299039 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981327 | TTTTGGACAAAATGT[C/T]GGTCCGTGATATAAA | 10477 |
rs576358789 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020707 | GGGAATGCCTAAACT[A/C]GTCTTCATATAGAGC | 10477 |
rs576365384 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060887 | TTTTTTTTTTTTTTT[-/TT]AGTTAGCTTTAAATG | 10477 |
rs576394453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027511 | AATTCTTGAGATTTA[A/C]CTTAAAAATATAAGT | 10477 |
rs576451031 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052981 | GACACCTCGCCATCA[C/G]TTTTACAATGCTGTT | 10477 |
rs576459936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033264 | TGGAGGCATCACGCT[A/C]CCTGACTTCAAACTA | 10477 |
rs576462860 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053691 | AATCGATAAACCTAC[A/G]TTAACACATCATTAT | 10477 |
rs576471507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026093 | TGGGGAGGCTTTTGC[A/G]TAGAATCAAATCTGT | 10477 |
rs576501227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990714 | TAGGCTGGTTATATC[C/T]ATTATGTTCTACTAG | 10477 |
rs576548835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031264 | GTTTTCATTAAATCA[C/T]GTTCATTTATTATGT | 10477 |
rs576628282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007236 | GAGAGAAAGAAGTGA[C/G]CCTGCAGGTTTTCAG | 10477 |
rs576667857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996404 | ACTGAGGGGGTAGTT[G/T]AAGGTAGAACGCAAA | 10477 |
rs576700986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002504 | ATTTGATTGCCATGA[C/T]TTACAACAGTGCTTT | 10477 |
rs576704136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049453 | GTACTTGTAGAAATG[C/T]TTTCATCTACATTTA | 10477 |
rs576715163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002089 | TAGCTAGAAATACAT[A/G]TGGCCTTCCACACCT | 10477 |
rs576718168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035576 | AATATATTAGTAATG[A/T]TACATAGCAAGCTTG | 10477 |
rs576885337 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012833 | ATAGGCATGAATTTA[C/G]AGATACTAACAAGTA | 10477 |
rs576895615 | snp | A/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982233 | TATCCACTAGTGCTA[A/G]AAGGTAATGTGTAAA | 10477 |
rs576915851 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994747 | ACTTGCAGGTGAATG[A/G]TGTAGCCTAGAAATA | 10477 |
rs576942719 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980868 | TTTTTTCCCTCCCCC[A/C]CCTTCCCCCCCCCAC | 10477 |
rs576975825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000841 | ACTTTTTAAATTCAT[A/C]AGCAAAATCGTAAAG | 10477 |
rs577026776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989316 | CTCATTCATTTTTGT[A/G]TCTTTTCCTTACTTC | 10477 |
rs577028913 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979953 | ACTTCCCTTTGGCAG[C/G]GACAGTTGCAAGCTA | 10477 |
rs577041241 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000439 | TGTACAACTCCAGGG[G/T]GTACCATTCATACTG | 10477 |
rs577055739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041499 | AGGCTAGATTGTAGT[G/T]GCACAACCGGCTCAC | 10477 |
rs577107204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048661 | CACTCCTCTCACCCT[A/T]ATTGTCTGTATTATA | 10477 |
rs577126804 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019256 | TGAACCGCCGCACCC[A/G]GCCTAGCTCTAAAAT | 10477 |
rs577165343 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055225 | TTGAGATGGAAACTC[A/G/T]AAGGGAGAGAGAAAT | 10477 |
rs577165389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048095 | CAGCTTCTACTGATA[A/C]ACCCCCACTGGGGTA | 10477 |
rs577169907 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996686 | CACTTGGCACTTGCA[A/G]ATTACTGGCCTAGAT | 10477 |
rs577191545 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059664 | TCTAGTTCGTCTCAA[C/T]TCACCTTGCCACAAT | 10477 |
rs577205932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996297 | TCTCCTAGCCACTTC[C/T]TTGTCAGTTGTCAGA | 10477 |
rs577208597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003136 | TGACAGGAAGTATAA[C/T]ATATGTGCCTTAATT | 10477 |
rs577219295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008499 | TCATAGATGCTTCGT[A/G]TGTGCATTTCTAGTT | 10477 |
rs577221247 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002705 | TTGAAATGTAGTGTT[A/G]AAATATACACCACCT | 10477 |
rs577227629 | snp | G/T | 0.000154149 | 0.00877784 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062776 | TAGCTTTTAATGTTC[G/T]TTCTGCTTTTCCAGC | 10477 |
rs577269897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043026 | CTGGTGAGCAAGGAA[A/G]CTTAAAAGTCAAGTC | 10477 |
rs577292777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995676 | TTTAATATCTTTCTT[C/T]ATCCTTAGTGTTTCT | 10477 |
rs577303747 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042758 | CCCAGGCCAAATGTG[C/T]TAAGTATCTGGGTTG | 10477 |
rs577333686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042518 | AGTAGTCATCAGGGA[A/G]GTAGGAAGAAATGGC | 10477 |
rs577351509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032166 | GCTTTTCTTGGGTTT[A/G]GAGGGCAAAATTAAC | 10477 |
rs577430660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013314 | GTTTGGGAGAGGAGT[A/G]GCTGCTAGCTGGGTG | 10477 |
rs577438984 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044584 | CAGTTTTAATTTACT[A/G]TGTAGAAACTACTTT | 10477 |
rs577440114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002024 | GAGATTGAAGGGCTT[A/G]AATATCCCAAGCAGC | 10477 |
rs577443103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984280 | ATACTTTTTAGCATA[A/C]GTATACATTGTGGAT | 10477 |
rs577567009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051595 | GATGCTAACTTGATA[A/G]CCTCATTGTGGGAAA | 10477 |
rs577575730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006176 | TGTAGGGTCAGAATT[C/T]GTATCACCAGGATAA | 10477 |
rs577698009 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998793 | TCAAAGCAACAGATA[-/C]GTTTTTATCCAAAAA | 10477 |
rs577703500 | in-del | -/TGAG | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983794 | CTGAGTACTAGTGGA[-/TGAG]TATTTCTCCAATCAA | 10477 |
rs577714579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057555 | ACATGCAAACACATT[A/G]GGGCTTATTTCTTTT | 10477 |
rs577785033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025085 | AGATACGTTCTGGGA[C/T]GAAAGTTGGAAGTAT | 10477 |
rs577795146 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010827 | TTTTTTTTTTTTTTA[C/T]ATTTTGCATGGATGT | 10477 |
rs577800219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050713 | ACCCTAGGCAAGTCA[C/T]TTAACCTTTCTGGCT | 10477 |
rs577818452 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020573 | TATTTCCTTTGTTTT[A/T]AATTCATAGTCATTT | 10477 |
rs577823377 | snp | A/C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042800 | AAAGAAAATTACATA[A/C/T]TAGTAGGAGCTGTCA | 10477 |
rs577863405 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035659 | ACACAAATTCGAAAA[A/C]TTCCTTGAAACATTA | 10477 |
rs577883538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991011 | ACAGTAATGTTTCTC[A/G]ACATTACTGTTTCCA | 10477 |
rs577903673 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063499 | GTTGATGAAGTAAAA[A/C]TGTGGCTATGAAGAT | 10477 |
rs577920224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059301 | CTTGAAGGATAATAA[A/C]TATTTAATAGAAATC | 10477 |
rs577933749 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056255 | ATACTTCTGTACATA[C/T]GTACAGGCAGGAGAA | 10477 |
rs577950704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016898 | TATGAAAGATAGGAA[A/G]GACCAAGGGCCCAGA | 10477 |
rs577966256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027388 | ACCTCTTGTTTTAAA[G/T]GAGAGACATAGTTAA | 10477 |
rs577971606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058777 | TGAATAAAAGAGGGT[G/T]ATTTCTCAGTAACTT | 10477 |
rs578011817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033211 | CACCAAAAAAGAGCC[C/T]GCATTGCCAAGACAA | 10477 |
rs578137222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991525 | GCCAAGACCACTACC[A/C]AGTGACTAGAGCAAG | 10477 |
rs578144304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034439 | AGAACAGAAAACCAA[A/C]CACCACAGGTTCTCA | 10477 |
rs578180112 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029866 | TTTTTGAGACGGAGT[C/G]TCTCTCTGTCGCCAG | 10477 |
rs578180398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034072 | GAACACTTTTACACT[A/G]TTGGTGGGACTGTAA | 10477 |
rs578189368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038353 | AGTAGGCTGTACCAT[C/G]TAGCTTTGTGTAAAT | 10477 |
rs578206574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997749 | TTTCCTATTACCTGA[A/G]TAAAAGTTGGGTTTT | 10477 |
rs745422935 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992149 | TTTTTTGTCTTGTAA[C/T]TTGTATGCTTAAGAG | 10477 |
rs745474282 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020953 | GGAATTTTTATCCTT[-/C]CTGTTTTGTAATATT | 10477 |
rs745511603 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002427 | CCTATCAATTCACAA[C/T]ACTTTTTTTGAAGAC | 10477 |
rs745573273 | snp | C/G/T | 8.57514e-05 | 0.00654746 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981999 | TTTTCTCCTCCTCCT[C/G/T]CCCTGTTCTCTTTAA | 10477 |
rs745577743 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055837 | GGAGAGTTTAAGGCG[A/T]ATGAGTCGTCTTACC | 10477 |
rs745635590 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059474 | TACATGTATAATTTT[A/T]AATTTTCTAATAGCC | 10477 |
rs745646811 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004961 | CAAAACTTTTATTTG[-/C]CATATACTTGCATAC | 10477 |
rs745659536 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037934 | GATCATACCACTGCA[C/T]TCTGGTCTGAGTGAC | 10477 |
rs745712641 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984147 | GAAAAATACCAAGAG[A/G]TTGATGTATTGTCTG | 10477 |
rs745742681 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049770 | TGCCAGAAATAGTTA[C/T]TAATTCTTCAATGAA | 10477 |
rs745768669 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021136 | CAATATACCAGTCTT[C/T]GTGGGCTTTCACATA | 10477 |
rs745774669 | snp | A/G | 1.68675e-05 | 0.00290405 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060837 | TCTTTATTAACATGT[A/G]CAATAAGACTACAAA | 10477 |
rs745802160 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006446 | ACTACTTCTGGATCT[A/T]GGATGGCCAGATAAA | 10477 |
rs745824262 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042091 | ATACCAGTTTTTCCA[-/C]CTAATGTCCTTTTTG | 10477 |
rs745868586 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007536 | TTATACTTGGAAATA[-/C]CTGGGCAAATAGCTA | 10477 |
rs745884768 | snp | A/T | 1.6894e-05 | 0.00290633 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060649 | TTCCTTCTGTTTTTA[A/T]TGTGACTGTGCTTAG | 10477 |
rs745978512 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005532 | TGAGTAGCAAAATTA[G/T]TATGTATCTTTTTGG | 10477 |
rs745987829 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043795 | TATAGTTTTGTGATC[C/T]ACTCTTCTTTCTTAA | 10477 |
rs746020436 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058840 | GGTATTTACCCCAAA[C/T]CGCAGACACCATTTA | 10477 |
rs746068424 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018077 | ACATTATGGGGCTGC[C/T]ACAGTGATTGTGCTT | 10477 |
rs746091349 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008326 | TGAATGTTATCCTCA[-/TT]TTGAGGTGAGAAAAC | 10477 |
rs746113801 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990885 | CAATTTTTACAAGTT[C/T]ACAATCCTTTATTTG | 10477 |
rs746125222 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014496 | TGATTGATTAGGGAA[A/G]GCTAAGGTCAACTTT | 10477 |
rs746141127 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994494 | TCAAAAGATAAGACT[C/T]CTTTTAACCATTGTG | 10477 |
rs746155458 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057597 | ACTTCTTATTGCTCT[A/T]GATTGCTAATTTACC | 10477 |
rs746167971 | snp | C/T | 1.68413e-05 | 0.00290178 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984036 | TCTCTTCTCATTTCA[C/T]TAACAGAATTCAGAA | 10477 |
rs746182887 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988075 | CTCCTCAGTTGTAAA[A/G]TGGGGATTAAAATGA | 10477 |
rs746224038 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054622 | TCATCGTATATTTTT[A/G]ATAACAGTTCTTTAT | 10477 |
rs746309704 | in-del | -/TG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997004 | ATAAATATGTGACTC[-/TG]TGTATCCCTTTGATC | 10477 |
rs746360542 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995890 | AATACAGCTCTAAAC[A/G]GAAACTTATTCTCAT | 10477 |
rs746363068 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036721 | ATAAGTGGGTAAACA[A/G]TACTCTAACTTGTTT | 10477 |
rs746369327 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983371 | ACACATCTAAAGTTT[G/T]GAAATCATCTTAAAT | 10477 |
rs746417803 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048207 | CCTTGCCTTTGTAGC[A/G]TTTTCTGTTTTATGT | 10477 |
rs746460212 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002332 | TCTGTTGCTCACTGC[A/G]TTAGGTAAGGCATCC | 10477 |
rs746491983 | snp | A/T | 1.65798e-05 | 0.00287917 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982173 | AACCTTCTGCCACCC[A/T]GCAGAAGAAAAACAC | 10477 |
rs746503680 | in-del | -/TTTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017723 | GTTTTTTTGTTTTTC[-/TTTG]TTTGTTTCCTAATTT | 10477 |
rs746544650 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041359 | GAAGCTTAGAACATA[C/T]TACTTTTTATATAGA | 10477 |
rs746550357 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986427 | AATTGGAATACTGAG[C/T]GTTTAGTAAAGGTGT | 10477 |
rs746566549 | in-del | -/TTTTTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs746577489 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055621 | ATACTACCATAGCTT[C/T]TCTGCTTAGTCTACT | 10477 |
rs746599634 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054227 | CAGGAGTGTGATTAC[G/T]GGATCTTATGGTAAG | 10477 |
rs746611206 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012111 | CTTTTGAGAGAGGGC[A/G]ATATGATCAGTCAGC | 10477 |
rs746708144 | in-del | -/AA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002621 | AAGATTTTTAAACTC[-/AA]ATATGAAAAATTACT | 10477 |
rs746722439 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052517 | AGCTGTTTAAGGTAT[A/T]TGCTCATTGCTTTTC | 10477 |
rs746763981 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026175 | ACACTGAAACCCTTT[-/G]GGAGGATTAAGTTAA | 10477 |
rs746799448 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048412 | ATTGTTAAAGCTTAA[A/G]TACTTTTTTTGATTC | 10477 |
rs746809455 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020072 | CTACTGTATTTCTTA[C/T]CTGTTTTTGTGGGAA | 10477 |
rs746825487 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060423 | AGATGGAATTACTGT[A/G]TCAGTTATTTAAGTA | 10477 |
rs746895340 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031705 | TGTTTTGTTTTGCTC[A/G]TAATTCCATTCCTTC | 10477 |
rs746907852 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991737 | GCTGCTGCTGCTGTG[G/T]CCCAGGGAAACCAAA | 10477 |
rs746954528 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010416 | GGGTGTACAAGTCGC[A/G]CTCTTATTGCAGCTG | 10477 |
rs746987851 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042598 | AAACTGGAAGTCATG[A/G]AACAGGTTAGAATTC | 10477 |
rs746999626 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017902 | ATTTTTTGGTTAGAG[A/G]AATCCCAGCTTCATG | 10477 |
rs747004282 | snp | G/T | 1.86069e-05 | 0.0030501 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062910 | TAATTTGTATGCAGT[G/T]TGAAGGAGCAGAAGG | 10477 |
rs747031662 | in-del | -/GTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018598 | TGTTTCAATTTCTGT[-/GTTT]TTTTTTTTTTTTTTT | 10477 |
rs747089588 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029286 | TAGGAGCTGCCTGAC[A/G]CATTCATATAAAATG | 10477 |
rs747208444 | in-del | -/AAAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999906 | AGCAGTTATATGGAC[-/AAAT]AAACAGGCATGTTTA | 10477 |
rs747223493 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989462 | CTATACATTCTTTAC[C/T]TTTTTCATAATTATG | 10477 |
rs747295236 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038798 | ATAGAGATGTTACTG[A/T]TGAAGCTGTATGAAT | 10477 |
rs747341555 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995518 | AAGTTTTTGGGGGCA[C/T]CAGAAGTTATACTCA | 10477 |
rs747363163 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985776 | AATGTTTTAAAATTG[C/G]ATGTAGGGTCAAACA | 10477 |
rs747380819 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014994 | GAACGGTGATGCCTG[A/G]TGAAGCAGCCCTTAA | 10477 |
rs747385433 | in-del | -/TCTC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028804 | ATGTTGCAAAAATCT[-/TCTC]TCTGTTAATGACTTG | 10477 |
rs747495696 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046714 | TCTTATTAATCTGAT[G/T]TTTCAGAATTAGAAA | 10477 |
rs747506668 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045724 | CAGATGTAGTAACCA[C/G]ATCAATTAACTTAGT | 10477 |
rs747511316 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005238 | TTAGACAGACTTTCT[C/T]CTTGTGATCATAAGA | 10477 |
rs747530569 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022538 | TAACTCGTGGCCAAC[-/A]GCACTATAACCATGC | 10477 |
rs747589011 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058746 | TGTATATGTGCACAT[A/G]AACGGATTTATTTTG | 10477 |
rs747596987 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999914 | TATGGACAAATAAAC[A/C]GGCATGTTTATGAAA | 10477 |
rs747598571 | in-del | -/AAGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009448 | TACTAACCAGAAACA[-/AAGT]AAGATGGAAGTCCAC | 10477 |
rs747630222 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011803 | TAAAATGAATGAACC[A/T]TGTGTCCTCCTTTTA | 10477 |
rs747633619 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010451 | CATGTCAGTCTTATA[A/G]TCTGAAGAGTAGTGG | 10477 |
rs747680626 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052165 | ACACACCCACATCCT[A/G]TAAGAAAATGTAATA | 10477 |
rs747719678 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024254 | CAGAAAATGATTGAC[A/G]CTTTATGTGAGAGTA | 10477 |
rs747743362 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994542 | AATTTTCAGTAGCTC[C/T]GTAATCAGTCATTGT | 10477 |
rs747803836 | in-del | -/TAGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986700 | TTTGGCTTTCGTGTG[-/TAGT]TATTTAATCAGAATT | 10477 |
rs747850110 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988423 | TGAACAAATATTGTA[A/T]TCCTTTTAAAGGAAC | 10477 |
rs747866177 | snp | G/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063112 | CCTACTTGCAAGTCT[G/T]GCTTCTTTGGGATAT | 10477 |
rs747875521 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043423 | AAATTATTTAAAATA[C/T]TGTATAAAATTACTT | 10477 |
rs747881230 | in-del | -/TTTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005801 | GAATCTGAAGTTACC[-/TTTG]TTTGAGTTGTGAAAT | 10477 |
rs747885628 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019249 | ACAGGTGTGAACCGC[C/T]GCACCCGGCCTAGCT | 10477 |
rs747930625 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024437 | TTTGGAAACTGAGTT[C/T]CAGTCATCATGGAGT | 10477 |
rs748019851 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041125 | TGGCAGCACGTGCCT[A/G]TAGTCCCAGCTACTT | 10477 |
rs748068504 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041599 | CGCACCACCATGCCA[A/G]GCTAATTTTTGTATT | 10477 |
rs748095986 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030076 | TGACCTCATGATCCA[C/G]CTGCTTCGGCCTCCC | 10477 |
rs748122906 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013501 | AATGGCCCTAGTTTC[-/T]TGACTTGTTGGCCTA | 10477 |
rs748129934 | in-del | -/CT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058856 | CGCAGACACCATTTA[-/CT]CTCAATTACAGCTGT | 10477 |
rs748136512 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054102 | ATTCACCTACTGAAG[C/T]AACATCTTGATCACC | 10477 |
rs748138347 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989240 | AGTACTTTTTTCATG[C/G]TGTATTATAATATTT | 10477 |
rs748162249 | snp | A/G | 0.000741931 | 0.0192462 | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989890 | TTTTCAGGAAAATCA[A/G]CAAGTCTTGCATAGA | 10477 |
rs748183553 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014761 | TTTTTGAGATACATG[A/T]GATATATGATACCTT | 10477 |
rs748183922 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027789 | ACTCTTAACATTGCC[A/G]TAACTCTACTTTCCT | 10477 |
rs748184436 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040157 | CTTAAATTGGGGAGG[A/G]AAATATGTTTGCGTT | 10477 |
rs748246953 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032275 | CTTACTCACCTGGTA[A/G]CAATTGCATAAAATA | 10477 |
rs748345721 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978966 | TCAACTCCAAATTGG[A/C]TGGCTTTTGCTGTAA | 10477 |
rs748364733 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008838 | AGAGCTAAGCTTGAA[A/G]TAATTTTGTAGACAG | 10477 |
rs748393996 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005025 | TAAGTTACTTTTAAA[A/G]ATTGACTTTGAATGC | 10477 |
rs748431970 | snp | A/C/T | 3.30645e-05 | 0.00406588 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181057708 | TGCTGGGCCTAAAGG[A/C/T]GATAACATTTATGAA | 10477 |
rs748478641 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993769 | GTCCCGAAGAGAATC[C/G]ATCTCAGAAGATTGT | 10477 |
rs748518128 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034486 | GAACAATGAGAACAC[A/T]TGGACACAGGAAGGG | 10477 |
rs748540611 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045525 | ATATCTGCTCTCCCC[A/G]TCTCCAGTTGTTTTG | 10477 |
rs748566647 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004356 | AAGAAACAATACAGC[A/T]GAGTGTGGTGGCTCG | 10477 |
rs748567660 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037509 | ATGTTTGTGTCTTAG[-/T]TTTTACAAAAAAAGT | 10477 |
rs748583901 | snp | C/T | 1.71296e-05 | 0.00292652 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982002 | TCTCCTCCTCCTCCC[C/T]TGTTCTCTTTAAAAG | 10477 |
rs748593831 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044385 | TAGTTTGTATTATCT[A/G]TGGCACTATGTATGG | 10477 |
rs748669694 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056855 | TAGCAGTTTGTCTGG[A/G]TGATGAAACTTAACA | 10477 |
rs748675425 | in-del | -/TTTTTTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs748745324 | in-del | -/ACA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049208 | TGGATATTATACACC[-/ACA]ATGAATGTGAATATA | 10477 |
rs748747010 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984354 | GTGCTGATTTTTGTT[C/G]TGATGTATTTCTGTA | 10477 |
rs748752163 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009140 | GTCACTTGTCCTTCT[C/T]CTTTAGAATGTTCTA | 10477 |
rs748784437 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982398 | TTAGGTGGTATGTAA[A/G]CAACATTACTAGAAT | 10477 |
rs748809853 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062784 | AATGTTCTTTCTGCT[C/T]TTCCAGCGGATCCTC | 10477 |
rs748834960 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993753 | AATCCATTTATTCAG[A/G]GTCCCGAAGAGAATC | 10477 |
rs748845506 | in-del | -/TTCA | | | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979861 | CCCAAACTCTTCTCC[-/TTCA]TTCACTTTTAAGAAT | 10477 |
rs748861035 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034843 | CAACAGGTGAAATGA[G/T]TTGAGTAATAGAAAA | 10477 |
rs748870228 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033795 | ATCTGACAAAGGGCT[A/G]ATACCCAGAATCTAC | 10477 |
rs748882059 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004081 | CTTGGAGAGGCTGGG[A/G]TGGAGAGTTAAGAAA | 10477 |
rs748922789 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993039 | TGCCTTGCATCTTGT[A/C]TAAATGCAGTAGTAA | 10477 |
rs748939921 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059157 | CTCTGTTGCTGAGAT[A/G]TACAGTATTAACCAT | 10477 |
rs748945090 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024003 | TGTGTTTTATATTTC[-/T]TTTGCATTTGTAACC | 10477 |
rs749007755 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991206 | GTAGATAAGCAGTTA[C/T]GGCCCTCTATAATAG | 10477 |
rs749015228 | in-del | -/GCAAATGGCCCTAGTTTCTTGACTTGTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013483 | CCTCACTGGCTGTTG[-/GCAAATGGCCCTAGTTTCTTGACTTGTT]GGCCTACCTGTAGGC | 10477 |
rs749031203 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028326 | ATATTGGGTGTTCCA[G/T]GTTTATTTTGTTTTT | 10477 |
rs749073204 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000839 | TAACTTTTTAAATTC[A/G]TAAGCAAAATCGTAA | 10477 |
rs749085400 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028176 | CTATTAATGTAATTA[C/T]TATAATGTAATTATA | 10477 |
rs749089702 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999741 | TTAGACAAATGGAAG[C/T]TCAAGTCTTGGCTTT | 10477 |
rs749212211 | in-del | -/CCTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021554 | CTTTTAAATATACTC[-/CCTT]CCTTCCTTCCTTCCT | 10477 |
rs749237032 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010403 | TGGTAAGAGTAGTGG[G/T]TGTACAAGTCGCGCT | 10477 |
rs749245614 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046975 | AAAACTAGGTTTCCT[A/T]TTCACTACAGAGCAC | 10477 |
rs749317004 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050912 | TTCTTTCTTGTTTCA[A/G]CGTACAGTAATAGGT | 10477 |
rs749368338 | in-del | -/AAATA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037535 | AAAGTTTAAAAAATT[-/AAATA]AAATAACTTTTAAAA | 10477 |
rs749377477 | in-del | -/A | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990768 | GAAATAACATTGGAC[-/A]GTCATCAAAATTCAG | 10477 |
rs749384538 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036898 | GCCTGTGGTTAAATT[A/G]GTTTCAGTATATGTC | 10477 |
rs749511637 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019612 | TCATTGGGGAACACA[A/G]TGTACCAGTGATTTT | 10477 |
rs749686939 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043154 | TGAAATGCTCCAAGA[C/T]GTGAAACTTTTTGAG | 10477 |
rs749689358 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014501 | GATTAGGGAAGGCTA[A/G]GGTCAACTTTCAGTG | 10477 |
rs749715531 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052722 | GTTTGTAGTTTCTAA[C/T]CATATCAAGACCTAG | 10477 |
rs749772519 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988370 | TTCCTAGGAACTTGC[A/G]TAAAAAAGAAAATTA | 10477 |
rs749782260 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026559 | TGCTTTCCAAAGGCT[A/G]AGGAAACAGAAAGTG | 10477 |
rs749782349 | snp | C/G | 6.85401e-05 | 0.00585366 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984022 | TCAAATCCTTTTTGT[C/G]TCTTCTCATTTCACT | 10477 |
rs749820455 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025810 | CCAAGTCTTCTATAA[A/G]AACAATTCTAATGTC | 10477 |
rs749868230 | snp | C/T | 1.66297e-05 | 0.0028835 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982195 | GAAAAACACCAAACT[C/T]TCTAGCAAAACCACT | 10477 |
rs749869965 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037603 | TATTTTTGTACAGCT[A/G]TACACTGTGTTTGTG | 10477 |
rs749899589 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017415 | AGTTAGGGGCATGAG[G/T]GGGGTGGAAACCAAG | 10477 |
rs749935016 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057090 | GTTAAAGAAAGGCGG[A/G]AAGGACCCATATTAA | 10477 |
rs749981110 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181043973 | ATTTTGCTTTGAGCC[C/T]TCTTTTACAAAAACT | 10477 |
rs749987650 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015345 | CTTTGTGAACTAAAT[C/T]GGTGACTTGCATTTT | 10477 |
rs750011226 | snp | A/G | | | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989899 | AAATCAGCAAGTCTT[A/G]CATAGAGTGTAAGGA | 10477 |
rs750024317 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992521 | GTGGGTCCAGGGACT[A/G]TCTTGGGCAGCTCTT | 10477 |
rs750035907 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056554 | CTTGGGAACTAATTC[A/G]TTCTTGCTAGAGTGA | 10477 |
rs750044579 | snp | C/T | 6.63031e-05 | 0.00575736 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982167 | AAAGAAAACCTTCTG[C/T]CACCCAGCAGAAGAA | 10477 |
rs750087455 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027319 | ACAATATCCTGCTTT[G/T]TGCTTTTCTGTATAA | 10477 |
rs750095512 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999159 | AAAATTATAAAAGGT[A/C]GAATTTATTTATTAT | 10477 |
rs750143445 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993705 | TCCTTTACAAATGGA[C/T]CATTTTCTCACATTA | 10477 |
rs750172262 | snp | A/G | 1.75262e-05 | 0.0029602 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983999 | CCCTGGTTATTCTGT[A/G]GACTATATCAAATCC | 10477 |
rs750209475 | in-del | -/A | 1.71158e-05 | 0.00292534 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060842 | ATTAACATGTACAAT[-/A]AGACTACAAAAACGA | 10477 |
rs750216662 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009803 | CTATTTTATGGATTT[G/T]TTGATAACTAGAATG | 10477 |
rs750263548 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001710 | AGGAGCTGGGATTTC[A/G]AAGGTGACAGATTAG | 10477 |
rs750273592 | in-del | -/TTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985500 | TAAAATTAATTTCAC[-/TTTT]TTACTATGTTAATAT | 10477 |
rs750297599 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994227 | TAAAATAAGCACGTT[A/G]CAATTATCACTTTTC | 10477 |
rs750352623 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051912 | TTGTACCTAAAATTT[G/T]GTATCTGTTTTTAAG | 10477 |
rs750369426 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046182 | AGTATGAAGCTTTGT[A/G]ATTACATTGTCCACC | 10477 |
rs750398502 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008908 | CTTGCAGTATGTGCT[-/T]TTTTTTTTTTTTTTA | 10477 |
rs750447407 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979131 | ATATTCTATCTGTTC[A/G]TTCTGAGTGGAATAT | 10477 |
rs750451154 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019579 | GAGCTTCATTTGTAA[G/T]TATCTCAAAAATTAT | 10477 |
rs750487377 | snp | C/T | 1.76968e-05 | 0.00297457 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062891 | ATACGCAACATAATT[C/T]ACATAATTTGTATGC | 10477 |
rs750493208 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992569 | TCTGTGTATCTTGTA[G/T]CTCTGACATTTGGAA | 10477 |
rs750526986 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031402 | TTGCTGTATTACTAT[A/T]CCTTGAGGCTATTTT | 10477 |
rs750533055 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991854 | AATGTGAGATTTCAT[C/T]GTGCTACTTAGAATG | 10477 |
rs750548096 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017797 | TTGTCTTTCAGCTCC[A/G]AACTAAAACGGGTAT | 10477 |
rs750554607 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059336 | CATGAATGCTATTCT[A/G]TTCACTAGTTATAGC | 10477 |
rs750579971 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035606 | GTTCAACCCATGACC[C/T]GTGGGTCACATGCGT | 10477 |
rs750599566 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003003 | TGTTTTGAAACACAT[A/C]TCTCTGCCCATGTGT | 10477 |
rs750611202 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058634 | TAACTATGGTGAAAT[A/G]TTTTTCTTTTCCAAC | 10477 |
rs750689628 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001957 | TGTACATGTCTTTGC[C/T]TTAATAATGGAAGTT | 10477 |
rs750692386 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040999 | TGACGCCTGTAATCC[C/T]AGCACTTTGGGAGAC | 10477 |
rs750702306 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037052 | GAACAACAGTCCTCA[C/T]ATATAATGGTGGTTC | 10477 |
rs750769542 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998127 | ACAACAGCAACTGTG[C/T]TTGACCGTACTCCTT | 10477 |
rs750783406 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037415 | GCTCATGAGGACCCT[A/G]CAGTGGAACAGGATG | 10477 |
rs750807221 | in-del | -/A | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063221 | TATCTGTATGAAGTT[-/A]ATAAAAGTAGCTGTA | 10477 |
rs750822344 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050195 | CACTATTTCCTGAAC[A/G]GTTATTGAAGGTGTT | 10477 |
rs750899215 | in-del | -/CAGGCAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036082 | GGACTTGGCTCACAG[-/CAGGCAA]CAGGCAACATCTTGT | 10477 |
rs751007597 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003579 | TGTGATTTTACTCAG[C/T]ACCTGAATGTCATAA | 10477 |
rs751163276 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996030 | TCCTTTTCAGAATGA[C/T]TGTCACTTCATAATT | 10477 |
rs751169723 | in-del | -/CAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000985 | ATAATGTATGTTGTG[-/CAT]CATCAACTCATATCA | 10477 |
rs751188448 | snp | C/G | 1.74656e-05 | 0.00295508 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984008 | TTCTGTAGACTATAT[C/G]AAATCCTTTTTGTCT | 10477 |
rs751189944 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043177 | TTTTTGAGTTCCAAC[A/G]TGATGCTACGAGTTA | 10477 |
rs751191776 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037307 | CCTTATTTTTTTAAA[C/G]TTAACTCTAAAACAG | 10477 |
rs751220568 | snp | A/G | 0.000196666 | 0.00991434 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984136 | TTCAAATTGTGGAAA[A/G]ATACCAAGAGATTGA | 10477 |
rs751398674 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032462 | CTCTGTAGTAGATAG[C/T]GTGGATAAGATAATG | 10477 |
rs751406595 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003814 | AATATGATTTCAAAT[G/T]CATTACTTGTTCAGT | 10477 |
rs751481866 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015188 | GTGGAATCCTATACA[C/T]GTGAATTTAGTATAA | 10477 |
rs751489583 | in-del | -/AAG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023526 | ATTGCTTTGTGGCAC[-/AAG]AAGACAGAGGAATTC | 10477 |
rs751532387 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043846 | ATGTCATTAAACAGT[C/G]TTCAAAATCTTCAAT | 10477 |
rs751584708 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990821 | GTTAGAAATGTGTGC[C/T]CTTCATTTGGGTTTT | 10477 |
rs751611700 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001803 | GAGAACAAGCTGGAT[G/T]CAGTTCACCTTTCAT | 10477 |
rs751648913 | in-del | -/T | 0.000117877 | 0.00767623 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984036 | CTCTTCTCATTTCAC[-/T]TAACAGAATTCAGAA | 10477 |
rs751703762 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012413 | ATTTTAGGTACTTTA[A/T]TAGCTCTTTAAATTA | 10477 |
rs751720522 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011230 | ACTCATGTTATGGAG[G/T]CTAGAAAATCCAATA | 10477 |
rs751739996 | in-del | -/GAACATACTCGTTTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053419 | CAGAACAAATTTTTG[-/GAACATACTCGTTTA]TAAAAGTTAGTAACT | 10477 |
rs751743149 | in-del | AGACTCCGTCTC/GAGAAAAACCCCCTCTCA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041223 | ACTAACGACAGAGCA[lengthTooLong]AAAAAAAAAAAAAAA | 10477 |
rs751756250 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039784 | TGGGGGATTGGTTCT[A/G]GGACTTCCACAGATA | 10477 |
rs751761094 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986179 | CTGTGATGACTATCA[A/G]CTGCTGCAAATGACA | 10477 |
rs751770419 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018021 | TTTCTACCTAGAAGA[C/T]CACCCTAATTTTGTT | 10477 |
rs751821818 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019787 | AATCACCATAAGCTA[C/G]TTAACGTAGCCTTCA | 10477 |
rs751832986 | snp | A/T | 4.99813e-05 | 0.00499881 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057671 | TATATGTACATACTG[A/T]TTTTTAATTTCTTTT | 10477 |
rs751904638 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048013 | CTTCCAGGCCCTGCT[A/C]CTTGTTCCTGATGGC | 10477 |
rs751916962 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019424 | TGTAATATAAACTTT[C/T]AAACTTTCAAAATTC | 10477 |
rs751974997 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978835 | ACCCCACTAAATCCT[A/G]TCAGCAATTGGCCTT | 10477 |
rs752014804 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006035 | GGCTAAGGACTGGGA[C/G]GCTGTCATAGTTGGA | 10477 |
rs752087014 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025057 | TTTCATGTGGCTTTA[C/G]TTAGCCACATGGAGA | 10477 |
rs752097038 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996639 | CTGCCTCTTCCCCCC[A/C]ATTTCCAGGTATCTT | 10477 |
rs752123961 | snp | C/T | 1.67885e-05 | 0.00289724 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057861 | TCTTTAGTATTTAAT[C/T]CTTCTCCTCTAAAAT | 10477 |
rs752155190 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986387 | TTGTGGGTGGAAGAA[C/G]ACCTAGTTTTTGTCC | 10477 |
rs752168542 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058987 | GTTTTCCTGGACACC[-/T]TTTAATGAAAAACAG | 10477 |
rs752184984 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006908 | TTTCAATTTCTCAGA[A/G]TAAAATTACTTTAAA | 10477 |
rs752213077 | snp | A/C | 0.00020033 | 0.0100062 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984143 | TGTGGAAAAATACCA[A/C]GAGATTGATGTATTG | 10477 |
rs752293713 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995356 | CAAGCTTACAATATT[C/G]ATAAATACAGTATAG | 10477 |
rs752319016 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035754 | GTGACCCAAGACAAT[G/T]CTTTTTTTAGTGTGG | 10477 |
rs752339014 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047801 | GCAGCCTGAGGAGGC[C/T]TTGCAAAATGTCCAT | 10477 |
rs752379661 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005941 | TGGCAATTTCTTAGA[A/G]GAGGCTGTAGCCCAG | 10477 |
rs752381320 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043704 | TCAATGTTATTTCCA[C/G]CCATCCTCTTTTAAA | 10477 |
rs752428650 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978586 | TAAACTCCATGACTT[C/G]AAGTTCGCCAAAGAA | 10477 |
rs752488005 | in-del | -/ACA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984184 | TGTGCAGCAGAGGAG[-/ACA]ACATTTGCTTCTTTA | 10477 |
rs752499088 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003061 | ATGTGTGCTTTTTGT[C/T]TTGAGAGAGTCTCTC | 10477 |
rs752517671 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019034 | GTGGTGTGATCTCTG[-/C]CTCACTGCAACCTCT | 10477 |
rs752585931 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013822 | CCAAATTCAAAGGGA[A/G]CAGAAATAGACCATG | 10477 |
rs752587239 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002192 | GTTTTAATGGATTTC[G/T]TTTTTTACTGAAAAT | 10477 |
rs752664657 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055277 | TAAAGTTGGGAGAAA[A/G]GGCATTGTTGGATTC | 10477 |
rs752666882 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014245 | GGGGGAACATTTTAA[A/G]TTCATTTCTGAACAA | 10477 |
rs752778145 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010969 | TCCTGCTGAAGGCTT[A/G]CCAGCTTCAACTTCG | 10477 |
rs752819558 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009744 | TGACTCCCGTACTGT[A/G]AAGTACAAGCTAAGA | 10477 |
rs752845276 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050501 | AATAATCCAAATTAT[A/G]TGAAGCATTTAAAAG | 10477 |
rs752847105 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022962 | GAAGTCAAAAATACA[A/G]TTAATGCTGGTAATA | 10477 |
rs752853508 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022397 | AATACTGAACCATTA[C/T]TCCTAGGGGAAATAA | 10477 |
rs752857653 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051553 | GCTCCTCTTTCTAAT[C/T]TCTCCTACCCCCATT | 10477 |
rs752860676 | snp | A/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063768 | GTTGCTTCCAAATTG[A/T]TGATTTTTGTTCAGC | 10477 |
rs752863411 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994120 | GTGTCCTTGTAAAAT[A/T]TTAAAAGACATTTTT | 10477 |
rs752879368 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985029 | TTTTTGCTACAAGTT[G/T]TATTCACTTGGGATG | 10477 |
rs752885082 | snp | C/T | 8.49336e-05 | 0.0065161 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057877 | CTTCTCCTCTAAAAT[C/T]GGTTATTCTAGAACT | 10477 |
rs752899418 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000593 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGCAGTG | 10477 |
rs753013480 | snp | C/G | 1.67607e-05 | 0.00289483 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060818 | TGCAACCCTGGTAAG[C/G]AAATCTTTATTAACA | 10477 |
rs753031283 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058523 | GGTCAAGTCAGCAGG[G/T]AAAAACCACTGGAAT | 10477 |
rs753052106 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039437 | TGGGAGGGCGACTTA[C/T]AACTAGAATGCCTGT | 10477 |
rs753130739 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030353 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 10477 |
rs753139331 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011075 | GGTGACTTGAGCACA[-/G]GGTCTTGACTTTTTT | 10477 |
rs753143464 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040583 | ACATCTAAACATTTA[A/T]TGTTAGAATGAAATG | 10477 |
rs753189177 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008288 | ATGTGGCAGGCAATA[G/T]TGTAAGTCTCAAAGC | 10477 |
rs753204483 | in-del | -/TTAG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006795 | TGCAAATAGTAAATA[-/TTAG]TTAGAAACCCTTTGG | 10477 |
rs753213878 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000485 | ATAGCACAGCACAGA[C/G]TAAGTATAGTATAAA | 10477 |
rs753231334 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035679 | TTGAAACATTATTAG[A/T]TTTTTTTTGCAATTT | 10477 |
rs753255264 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060067 | AAAAACCTTGTTTAT[C/T]TTATTTTAATATTTT | 10477 |
rs753349269 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046444 | GTTTAGTTTAAGCCT[C/T]ATGATAAACTGGGCT | 10477 |
rs753428362 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004957 | AAACCCAAAACTTTT[A/G]TTTGCATATACTTGC | 10477 |
rs753441328 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027654 | AGCAAGAGTGCTGCA[-/G]CATGTTGTGTCTTTT | 10477 |
rs753527308 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057190 | TTAAAAGGGTATTAC[C/T]GAATCAGTTGACAAC | 10477 |
rs753534670 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990550 | TATTATTTGTCATAC[A/G]TGTGTGTTATTTTTT | 10477 |
rs753629244 | snp | C/G | 1.71764e-05 | 0.00293051 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981994 | TAACATTTTCTCCTC[C/G]TCCTCCCCTGTTCTC | 10477 |
rs753634049 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030589 | AGAGAAAAAAAATTA[-/T]TTTTTTTATTTTTTA | 10477 |
rs753646505 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012744 | TTGTAATTACAATCT[A/G]GGTTTTGAATTATGG | 10477 |
rs753699855 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051197 | AATGGTATTAAATTA[C/T]ATGTTTAATCCTTCA | 10477 |
rs753700691 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986361 | TATCCAGATACTTTG[C/T]CTTCAAATTCTTGTG | 10477 |
rs753729488 | snp | C/T | 1.65798e-05 | 0.00287917 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982137 | CAGCCGCTCCAGAGC[C/T]TGAAGAACAAGAGGA | 10477 |
rs753738513 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011408 | TTTTATAATTAACTC[A/T]CTCTAGGGTGGAGCT | 10477 |
rs753766098 | snp | C/G | 1.71669e-05 | 0.00292971 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982273 | CAGCACACTTTGTCA[C/G]GTTGTCTTCCAGGTG | 10477 |
rs753785164 | in-del | -/TA/TTG | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991152 | AAAAACCTTTGATTT[-/TA/TTG]TTTTTTCTTTTTTTT | 10477 |
rs753786496 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995114 | ATCACTCCAGTAAAT[C/T]GTGTATTGCGGTAAA | 10477 |
rs753829952 | in-del | -/T | 0.00238398 | 0.0344428 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990021 | AGAAATAGAAAGTGA[-/T]TTTTTTTTTCCACAT | 10477 |
rs753845760 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022263 | TGAAAATAAGATTAG[G/T]ATTATTGCTAGCTCT | 10477 |
rs753861976 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007805 | CTTGATATCTGCCAC[-/AT]GTGGGAAATCGAACA | 10477 |
rs753876261 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008479 | GTAAATTGTTCTTAA[A/C]GTGGTCATAGATGCT | 10477 |
rs753893601 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049597 | TAATAGGCCTTAAGA[C/T]AGACAAAGCACAAGC | 10477 |
rs753935982 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983082 | AATATCCACAAACTC[C/T]AGTAATTATACATAA | 10477 |
rs753970756 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020658 | TTTGTTTCTTGTGTC[G/T]AAGTTCAAATAAAAG | 10477 |
rs753985487 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035526 | TGTATACTTTAATAA[A/G]CATGTAAAAAGCATG | 10477 |
rs754040299 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993492 | TGCTTTTGGGAGTAT[A/G]GTTCCACATCTTTTG | 10477 |
rs754084785 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015756 | AAGAGAAAATCTTAA[A/T]AGAATGCACAGAAGC | 10477 |
rs754281312 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039573 | CTCAGGAGTTTGAGA[C/T]CATCCTGAGCAACAT | 10477 |
rs754281386 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027370 | TATATCATGGTCATC[C/G]AAACCTCTTGTTTTA | 10477 |
rs754327256 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009455 | CAGAAACAAAGTAAG[A/G]TGGAAGTCCACCACA | 10477 |
rs754415519 | in-del | -/CAAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023392 | TGTCTTCTGATTTCT[-/CAAA]CAATGTATATTGCCA | 10477 |
rs754438160 | in-del | -/CAGTATACA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009613 | TAACCAAATATATTT[-/CAGTATACA]CAGTATACACCAAAA | 10477 |
rs754448138 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027449 | ATAGGAACTATTTGA[A/C]CCATTAAATAAAAAG | 10477 |
rs754499038 | snp | C/T | 1.72809e-05 | 0.00293941 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984017 | CTATATCAAATCCTT[C/T]TTGTCTCTTCTCATT | 10477 |
rs754514033 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994486 | ATGCACTTTCAAAAG[A/G]TAAGACTCCTTTTAA | 10477 |
rs754565247 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004986 | GCATACTGTCAGCCT[A/G]TAAGACAAACTCAGC | 10477 |
rs754574235 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057364 | CTCAGAAAAAAGTAT[A/G]TCTCTATGCATGCTT | 10477 |
rs754628497 | snp | A/C | 1.81365e-05 | 0.0030113 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984140 | AATTGTGGAAAAATA[A/C]CAAGAGATTGATGTA | 10477 |
rs754655210 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017619 | AGACTGGATTCATCT[A/G]TGCCTTCCTACTCTG | 10477 |
rs754700835 | in-del | -/CCCCCAA | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987886 | TGCAGACTCTTGCTT[-/CCCCCAA]CCCCCAACCCCCAAC | 10477 |
rs754751461 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014186 | GGAGGGTGTAAAGAT[G/T]GAAGTTTTAGTTTTT | 10477 |
rs754827125 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012802 | TTAGACTAAAGTTTT[A/G]TTATCTAACCCATGT | 10477 |
rs754915224 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011426 | CTAGGGTGGAGCTCC[C/T]GCAGCCCAGTTACCT | 10477 |
rs754979054 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050374 | TAAAAGACTCTAAAA[C/G]TCATCTTGTCACCTG | 10477 |
rs754983849 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012286 | GTAAATTTTCAAATA[C/T]AACTGAAGCAAATAT | 10477 |
rs754988034 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024221 | TCTTCCAAGATGAGC[C/T]TCTTGACTGACTCTT | 10477 |
rs755028081 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981516 | AGTGTTGTGTTTAAA[C/G]GCTTTACGTGCACTG | 10477 |
rs755062330 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008500 | CATAGATGCTTCGTA[C/T]GTGCATTTCTAGTTC | 10477 |
rs755083992 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048757 | TCAGGAATAACAACT[A/G]TTCACTTATAAACAG | 10477 |
rs755135022 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983083 | ATATCCACAAACTCT[A/C]GTAATTATACATAAA | 10477 |
rs755174809 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020086 | ATCTGTTTTTGTGGG[A/G]AGGTTGATGTATTAG | 10477 |
rs755209095 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998865 | AATCAACAGATGATT[C/G]ATTTGAAAACCATAA | 10477 |
rs755220809 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981419 | TTTTCCCAGGGTGGC[A/G]GCTCGGTCTTGGCCG | 10477 |
rs755326020 | snp | C/G | 6.7271e-05 | 0.00579922 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057865 | TAGTATTTAATCCTT[C/G]TCCTCTAAAATCGGT | 10477 |
rs755353495 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991086 | CTACAAATAGTTTCA[A/G]GTCAGTTCACATTTA | 10477 |
rs755384718 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015955 | ATATAGTACCATGGA[A/G]CATGTTAGAGCAATG | 10477 |
rs755403171 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990250 | GGAGAAGGGGGCTAC[C/T]ACTGACATTAGTAGG | 10477 |
rs755410661 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029003 | CCAAATTTATTTGGA[A/G]TTGATTCTTTGAAAA | 10477 |
rs755418531 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989134 | TCTGGGGACTTGGGC[A/G]TTAGTGATAATTTTA | 10477 |
rs755441084 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058838 | GTGGTATTTACCCCA[A/G]ACCGCAGACACCATT | 10477 |
rs755486917 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999236 | AGAATGGCAGTTCCT[A/G]GTACTCTGACGTTCC | 10477 |
rs755512864 | in-del | -/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990089 | TTGGAATCTGGAAGC[-/T]GAAACATCTTCAAAC | 10477 |
rs755515238 | in-del | -/TG | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979629 | GTATTCTGGCTACTT[-/TG]TGCCGTGGGGTAAAA | 10477 |
rs755518052 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989691 | CATTTTTATTAAGGA[C/T]CTATTAAGTTCAATG | 10477 |
rs755575257 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998791 | CTCAAAGCAACAGAT[-/A]ACGTTTTTATCCAAA | 10477 |
rs755594407 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038394 | GTTTGAAAAATGACA[A/G]AATCCCCGAATGACA | 10477 |
rs755620190 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045269 | TTACAGCTTTTTGAG[A/G]TGGTGATAGGGAAGT | 10477 |
rs755628064 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004044 | CTGCCTGCATCAGGT[A/G]TGAATGTGTGTGTGG | 10477 |
rs755641524 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023846 | ACATGGAAAGTTCAT[-/A]AACTGGTGCCCTCCA | 10477 |
rs755674072 | snp | G/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044027 | TCCTAGGATAGCTTC[G/T]TGGATGTGGGATTAC | 10477 |
rs755688652 | snp | A/G | 3.67316e-05 | 0.00428538 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984145 | TGGAAAAATACCAAG[A/G]GATTGATGTATTGTC | 10477 |
rs755715950 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057148 | TGGTTCCAAGACTGG[C/G]TCCTGCATCGGAGAA | 10477 |
rs755728972 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056617 | TCATGAGGGATCTAC[C/T]CCTCTGACCCAGACA | 10477 |
rs755763755 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027349 | AGAGACTTGGTAGCT[A/G]CATCATATATCATGG | 10477 |
rs755834753 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014431 | TAGGTGAGTGTAAAC[A/G]GAGAGGATGAAAAGA | 10477 |
rs755882658 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985289 | GCTGTCCGGTAATGT[A/G]GCCACTTGCCACATG | 10477 |
rs755930690 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998045 | GCCGTAGCACTAACT[A/G]TGAGAATAATTTTAA | 10477 |
rs755939402 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028071 | TTCATTCATTTCCTT[-/A]CTTCTTATAAAAATA | 10477 |
rs756090645 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980142 | AGTCTCCCGTCTCCC[A/G]GGGCGGCGGGGGACT | 10477 |
rs756100454 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993685 | GCCATTTACAGTCTT[A/T]TAGGTCCTTTACAAA | 10477 |
rs756102976 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004863 | TTGCCAAATGTAATT[G/T]TGAATGCTAGTGTTT | 10477 |
rs756168716 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034813 | GAACAAGTTTCCATG[A/T]ACAAATGTGGCTTTC | 10477 |
rs756179793 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992600 | CATATGCCTCAAGCA[A/G]TCCTCCCACCTCAGC | 10477 |
rs756199049 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019600 | CAAAAATTATTTTCA[C/T]TGGGGAACACAATGT | 10477 |
rs756238565 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979247 | TTAGTCACACAGCAA[C/T]TGAATGAGTGTATGT | 10477 |
rs756288665 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992551 | TCTCTGTGTTGACTT[A/G]TATCTGTGTATCTTG | 10477 |
rs756290635 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019198 | TTCCTGACCTCAAGG[A/G]ATCCACCTGCCTTGG | 10477 |
rs756290705 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031404 | GCTGTATTACTATAC[A/C]TTGAGGCTATTTTAT | 10477 |
rs756306953 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982432 | ACTTTTAAGCAAACT[G/T]AATTCTGTACTTCGG | 10477 |
rs756328604 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991995 | GGTAGGGACTGCTCT[A/G]CTACTTCTGTTACGT | 10477 |
rs756371999 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020493 | CTTTTAGGGGCCTAC[A/G]ATTCAAGCTGTCACA | 10477 |
rs756378490 | snp | A/G | 3.43442e-05 | 0.00414378 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060617 | TTAGTGTTTTAATTG[A/G]TAATACAGCATTCAT | 10477 |
rs756378877 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030637 | CGTTTTAAGAGTGGA[A/G]TGATCTCACTTGAAA | 10477 |
rs756414592 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042163 | GTCTACCCTATCCCC[A/G]TCAGTCATTCTAAGC | 10477 |
rs756487448 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988940 | ACCCGCTTTTTATAA[A/T]AATTAAATCTTAATT | 10477 |
rs756503604 | snp | A/G | 1.67691e-05 | 0.00289556 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060820 | CAACCCTGGTAAGCA[A/G]ATCTTTATTAACATG | 10477 |
rs756534650 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038332 | TACCATATAACCTAA[C/G]TGTGTAGTAGGCTGT | 10477 |
rs756565653 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023024 | ACTTAATGTTTTTTA[C/T]GATGGTGAGAAAGCA | 10477 |
rs756577356 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988173 | GTAAATCGAGTCAGT[A/G]AAGTGGCCACAGCAA | 10477 |
rs756606706 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019792 | CCATAAGCTAGTTAA[C/T]GTAGCCTTCACCTTA | 10477 |
rs756649587 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007344 | AGAAAGAAGGCTAGC[A/G]TGTTTTCCACGCAAT | 10477 |
rs756719830 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992358 | ATACTTAATACTTTG[A/G]ATGTATTTTGCCTTG | 10477 |
rs756770533 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014370 | GTTGGAAATTATTTG[A/C]GTATTTTAGGTGTAT | 10477 |
rs756791509 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056421 | CTGCATCTGTTGAGG[A/G]CCTCAGGCTGCTTCA | 10477 |
rs756830487 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020835 | TCATTATATCTGGAT[A/T]TCCCTGACATGGGTA | 10477 |
rs756896058 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041137 | CCTGTAGTCCCAGCT[A/G]CTTGGGTGGCTGAGG | 10477 |
rs756907162 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037322 | GTTAACTCTAAAACA[A/G]CCTCAGGCAGTTCTT | 10477 |
rs757018520 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030717 | TGGGATAAGGTGGGG[A/G]AAAGGTGGAAATTAA | 10477 |
rs757028273 | snp | A/G | 3.31494e-05 | 0.00407107 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982147 | AGAGCCTGAAGAACA[A/G]GAGGAAAGAAAACCT | 10477 |
rs757029718 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993607 | CCCTTTACATCCATG[C/T]GTCTCACTTTTTATA | 10477 |
rs757056933 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037617 | ATACACTGTGTTTGT[-/G]GTTTTAAGCTCAGTG | 10477 |
rs757057398 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983958 | GCCTTGCATTTAACT[G/T]CATGGTGGTAGAGGG | 10477 |
rs757069703 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979905 | TTTTAAACACTGTTT[C/T]GGATTTTTAAGGTTT | 10477 |
rs757089602 | snp | C/G/T | 0.000119254 | 0.00772103 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060635 | ATACAGCATTCATTT[C/G/T]CCTTCTGTTTTTAAT | 10477 |
rs757151470 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981931 | TTTTTCATTACAAGA[C/G]GATTTTAGATGACTA | 10477 |
rs757178849 | in-del | -/CCC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021574 | CCTTCCTTCCTTCCT[-/CCC]TCCCTCCCTTCCTTC | 10477 |
rs757214850 | in-del | -/T | 0.00238398 | 0.0344428 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990022 | AGAAATAGAAAGTGA[-/T]TTTTTTTTCCACATA | 10477 |
rs757249077 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015291 | AGTCACATTAGGACA[G/T]TTTAAAATGAGGGCT | 10477 |
rs757257289 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011271 | GGCAGGACCTTCTTT[-/C]TAGGATGCTGCTTAT | 10477 |
rs757279014 | snp | C/T | 1.6799e-05 | 0.00289814 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060829 | TAAGCAAATCTTTAT[C/T]AACATGTACAATAAG | 10477 |
rs757425286 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057089 | AGTTAAAGAAAGGCG[G/T]AAAGGACCCATATTA | 10477 |
rs757485662 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053753 | ACTCTTGATGTTGTA[C/G]ATTTTATGGATTTTT | 10477 |
rs757491556 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039800 | GGACTTCCACAGATA[C/T]CAAAATTCTCAAAAT | 10477 |
rs757492477 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999660 | AAAAAAAAGAAAACC[A/C]AAATATAAAACAGAC | 10477 |
rs757544681 | snp | C/T | 1.72475e-05 | 0.00293657 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181062879 | GTGGACCAAGAGATA[C/T]GCAACATAATTCACA | 10477 |
rs757623286 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011248 | AGAAAATCCAATATC[A/G]GGGTGCTGGCAGGAC | 10477 |
rs757628212 | in-del | -/TATT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029490 | TTTTCTGTATTCAAG[-/TATT]TATTGTACATCTTTT | 10477 |
rs757634797 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036611 | GGTTATGTGAAAGTG[A/T]GCCCAGTGATGCAGG | 10477 |
rs757705109 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995553 | TTTTCCTTTTTTTCT[A/G]ATCTATAAGGTTCTC | 10477 |
rs757711889 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046738 | TTAGAAAATCTCTGT[A/T]GTCAGAGTTCTCCAG | 10477 |
rs757735102 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019531 | GTTTTGCATTTTGAA[A/G]GAATAATAGAAACTA | 10477 |
rs757753633 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978853 | AGCAATTGGCCTTTG[A/G]GCCTTCAGGCTATTT | 10477 |
rs757786806 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006138 | AGCAAGGCAGAACTG[G/T]AGAGGGTAAGGAGGC | 10477 |
rs757848198 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059217 | AAGATTTCTGGTATA[A/T]TCTTGGTATTTGGAA | 10477 |
rs757860775 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023476 | TTTCACCTTTCATTT[A/G]ATAATAAGGAGTTTG | 10477 |
rs757871811 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987695 | GCAGTTGTTTCTAAA[A/C]CAGTAGTTGATAATC | 10477 |
rs757874004 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042731 | TTCAATTCTGAACAT[A/C]CATAATTGAGTCCCA | 10477 |
rs757888604 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025068 | TTTAGTTAGCCACAT[G/T]GAGATACGTTCTGGG | 10477 |
rs757930044 | in-del | -/GAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060540 | TTATTAAACCTAATC[-/GAT]TAAGTTTAGCTCCAG | 10477 |
rs757950891 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024257 | AAAATGATTGACACT[G/T]TATGTGAGAGTAAAA | 10477 |
rs757953682 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996752 | AGAAACCAATTTTAT[A/G]TAGCATTACTTTGAG | 10477 |
rs757967467 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995407 | TCCCTTATGATTTTC[C/T]TTTGCTTATTTTACT | 10477 |
rs757973193 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054131 | CCTTCAAGATTTGGC[A/G]GTTATGAATCAAGCT | 10477 |
rs757976409 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036490 | TCCCGTGTCTGTGTG[A/G]GCTTTCTCCGTGTAT | 10477 |
rs758099154 | snp | C/T | 1.65759e-05 | 0.00287883 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982168 | AAGAAAACCTTCTGC[C/T]ACCCAGCAGAAGAAA | 10477 |
rs758137713 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994581 | ACAAATGGGTGTTGT[C/T]CTTCCTTCCCCACAG | 10477 |
rs758169270 | in-del | -/A | 3.54578e-05 | 0.00421042 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060857 | AAGACTACAAAAACG[-/A]GTGCTTTTTTTTTTT | 10477 |
rs758184023 | snp | A/C | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063251 | AGATGGCTAGGAATT[A/C]TGTCATTTGTATTAA | 10477 |
rs758187937 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012107 | TTTTCTTTTGAGAGA[A/G]GGCAATATGATCAGT | 10477 |
rs758273413 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992030 | ATGACTGAAATTACT[C/T]ACTACTCATGATGAA | 10477 |
rs758323576 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984949 | GTGCTCAATAATGCG[A/C]GTGGCTGCAAGGAAT | 10477 |
rs758345475 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017867 | AAGGGAGTGATTGAC[A/G]AGGGCCCTGTTGCTA | 10477 |
rs758359065 | snp | A/G | 5.06342e-05 | 0.00503136 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060839 | TTTATTAACATGTAC[A/G]ATAAGACTACAAAAA | 10477 |
rs758401076 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039718 | ATGACAAAGACACTG[A/T]TGTCTAGGAGTTAAA | 10477 |
rs758421182 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055299 | GTTGGATTCTTATTG[A/G]CATCACTCACCAGAG | 10477 |
rs758497742 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027838 | AAAAAAGTAAATTCT[A/T]TTACTATGTAAGTAT | 10477 |
rs758569014 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046042 | GTGAGGGCAAGGACC[-/T]TGTATGTTCTTCTGT | 10477 |
rs758576957 | in-del | -/TA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018373 | CTCTGTGTGTGTGTA[-/TA]TATATATATATATTT | 10477 |
rs758584200 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038668 | TCACAGAAAGGGAGA[A/C]AATAATTTGAAAACC | 10477 |
rs758592541 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009859 | GGCACTTAGCTATAT[A/G]CTTTATAAATGCTTT | 10477 |
rs758627939 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050582 | CCTTTATTTCTGAAT[C/G]TGTTTACATTTTATT | 10477 |
rs758654274 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987950 | TTGTATATATAAGTA[G/T]GTTTGAAAAGTGCTG | 10477 |
rs758669935 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014730 | TTTTAAATTTTTATT[A/G]ATATAGTTATACATG | 10477 |
rs758738588 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057269 | AAATTGTAACTGTAT[C/T]GTAATTTATAGGAGA | 10477 |
rs758753943 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046614 | TCAGTTTTGGATGAG[C/T]CCTTAAACTGTACAG | 10477 |
rs758782386 | snp | A/C | 0.00011672 | 0.00763849 | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987415 | GGATTTCTAACTTAA[A/C]CCCTAATTTCTTTCC | 10477 |
rs758800105 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005105 | AGCTTAAGTAAAACA[G/T]AAATTTGTTGGCTCA | 10477 |
rs758830344 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057301 | TGTTTTTAGGAAATG[A/C]ACACTGACATGTTTA | 10477 |
rs758843085 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018915 | TCTCAGATTTTTCAT[C/T]GTAAAGTAAGGAAGT | 10477 |
rs758845308 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005032 | CTTTTAAAAATTGAC[C/T]TTGAATGCCTGTATC | 10477 |
rs758875045 | snp | C/T | 1.66754e-05 | 0.00288746 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057668 | TAATATATGTACATA[C/T]TGATTTTTAATTTCT | 10477 |
rs758895248 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030407 | TGTGTATATTTTTCT[A/G]ATGTCAGACTAACTT | 10477 |
rs758931764 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979603 | GCCTGGGTGGCAAAC[A/G]GGAAGTTTTTGTATT | 10477 |
rs758952553 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003590 | TCAGTACCTGAATGT[C/T]ATAAGTCAGTTTGCT | 10477 |
rs759031692 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029932 | ACCTCTGCCTCCAGG[G/T]TTCAAGTGATTCCCC | 10477 |
rs759090482 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005919 | GCTGGTAGTCTTGAA[A/C]TGCTTCTGGCAATTT | 10477 |
rs759137805 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978428 | TCTCTTTACTTCTTT[A/G]ATACAGCACTTCTCA | 10477 |
rs759140482 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003083 | GAGTCTCTCTGTTCC[-/T]TTTGAGAATGGAGTG | 10477 |
rs759192981 | snp | A/G | 1.66109e-05 | 0.00288187 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181057819 | TTATCCATTTAAGCC[A/G]CCAAAGGTAAGAAGC | 10477 |
rs759213265 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030978 | TATACTATTACGTTT[C/G]TTACCTTTTCTATTT | 10477 |
rs759231420 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018886 | GGATGTCAGGATAGA[C/T]CTAGGTTCCATGCTC | 10477 |
rs759263629 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988507 | AAAGTATAATAAACA[A/G]TTTTTAGATGAGTAA | 10477 |
rs759344315 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055240 | GAAGGGAGAGAGAAA[C/T]AGAGATTTTAAAAAA | 10477 |
rs759349821 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987549 | TCTTGATGTGGGAAA[G/T]GCCATATTGGGGGAT | 10477 |
rs759408446 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058000 | TGACTCCTTTCACAA[A/G]TAATTTGTAATAAAC | 10477 |
rs759435173 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036436 | ATGAGGAAAAAACCT[C/G]ATTCCTGGCAGGGGC | 10477 |
rs759437331 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996452 | TTAATTTGTCACAAT[A/C]ATTGAACTTAAATAT | 10477 |
rs759462055 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988700 | TTTTTTCTAATTGGC[A/G]TATGAAAGCAGGTAA | 10477 |
rs759473226 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037122 | ATTGAGGTTGTAGTC[A/T]TCGTAGCATCGTCAG | 10477 |
rs759490547 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996109 | TAGAATTTCTTAATT[-/G]TAAAAAAAACTTCAG | 10477 |
rs759533459 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048648 | TTATTTCCCCAGCCA[C/T]TCCTCTCACCCTAAT | 10477 |
rs759625855 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984936 | TGTGAAGAGATATGT[A/G]CTCAATAATGCGAGT | 10477 |
rs759626658 | snp | C/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063559 | CTTAAATTGAAAACA[C/T]TTAAAATCCTATTAA | 10477 |
rs759661213 | in-del | -/A | 0.000122888 | 0.00783766 | intron-variant, frameshift-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989900 | ATCAGCAAGTCTTGC[-/A]ATAGAGTGTAAGGAC | 10477 |
rs759666505 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024674 | TAAACATACAATAAA[A/G]CTGAAAATTTTAGTG | 10477 |
rs759715759 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993952 | AGATTTGTGATATAT[A/G]TGCTTGTACTAAATT | 10477 |
rs759803028 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993541 | GGGAAACATGAATTT[C/T]GTTACCTTTTTATTT | 10477 |
rs759823495 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993203 | TAATACCAATAGTGA[A/G]GATCAGCTTAGGGTC | 10477 |
rs759832433 | in-del | -/TTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018599 | GTTTCAATTTCTGTG[-/TTTTTT]TTTTTTTTTTTTCCA | 10477 |
rs759833914 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001505 | AAAAGAGACAATTTG[C/G]AGAAGGGATGGATTG | 10477 |
rs759857132 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003754 | TTTCCTTATATGATG[A/T]ATTGTTACAAGTATC | 10477 |
rs759869128 | in-del | -/TAAGA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028047 | ATGTGATCATTATTC[-/TAAGA]TGTTTTCATTCATTT | 10477 |
rs759901779 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008194 | TATGTTATTTTGCTT[A/G]TGATGTTTTGTTTCT | 10477 |
rs759906451 | snp | G/T | 1.66818e-05 | 0.00288802 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982099 | CACCAGCAGTGGCAG[G/T]TCAGATGCGGACCAG | 10477 |
rs759935711 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007113 | TGACCTAAATTTAAT[C/G]ATTTTTTTTTCCAGT | 10477 |
rs759992376 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992046 | ACTACTCATGATGAA[A/G]GGGTATTTTCATTTG | 10477 |
rs759997866 | in-del | -/AAAAC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052411 | GGCTGTTAAAAGCAT[-/AAAAC]AAAACAGCACAACAG | 10477 |
rs760000473 | snp | C/G | 1.69476e-05 | 0.00291093 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982253 | TAATGTGTAAAAGAA[C/G]GATCCAGCACACTTT | 10477 |
rs760063493 | in-del | -/TACTATAC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031396 | TAATCTTTGCTGTAT[-/TACTATAC]CTTGAGGCTATTTTA | 10477 |
rs760064700 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053526 | TGTTCTAAAATTTAT[G/T]TGTATTTTTTAAATT | 10477 |
rs760104666 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985880 | AGACATGTATTAAGT[A/G]CCCTCAGAGCAATAG | 10477 |
rs760110024 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031495 | TCATTTTAAAGTACC[A/C]CATTACTCTGTGTGT | 10477 |
rs760143227 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051364 | TTTAAACAATGCTAG[A/G]TTGGATATCTTCTCA | 10477 |
rs760144733 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058194 | AAAAGTAAAACTGTT[G/T]GACAGCTTCCAGAAA | 10477 |
rs760236517 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034247 | GTTTATTGTGGCAGT[A/G]TTCACAGTAGCAAAG | 10477 |
rs760237198 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017453 | CCTCCTGGATTAAGC[C/T]AACACTTTTTCTTCT | 10477 |
rs760247890 | snp | A/T | 1.67315e-05 | 0.00289231 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057646 | TTAGGATATTAACAT[A/T]CATTGCTAATATATG | 10477 |
rs760284907 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990546 | CTTATATTATTTGTC[A/G]TACGTGTGTGTTATT | 10477 |
rs760325329 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980465 | CACCCCCAGGGTGAG[A/G]GGAGGTGTGGAGAGC | 10477 |
rs760329332 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028749 | TTTGTTTTATTAGGG[A/G]TTCTTATGTATTGTG | 10477 |
rs760343656 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000116 | TTTAACCCAATTTCT[A/G]GATGTATTAGATACA | 10477 |
rs760399159 | snp | A/G | | | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989925 | AAGGACATTCAGATT[A/G]AGAATGAAGAACTTG | 10477 |
rs760401071 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001354 | TGGATTTCGAAAGTA[C/G]AATTTTCGAGCTTCT | 10477 |
rs760433230 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010587 | TGATCTGAGTTTCAC[A/G]GGTAGATATAAAAGG | 10477 |
rs760446224 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039397 | AAAAGTGGGTGCAGA[C/G]GAGCATTCTGGCTCC | 10477 |
rs760456636 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983693 | TCCAGTGCTTTCCCT[C/T]CTCCCTTTTTGTCTC | 10477 |
rs760484141 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995050 | TCTAGTGTTGCAAGT[A/G]TCTTCTTAAAACACT | 10477 |
rs760504733 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038737 | CTTAACATACAAGTC[-/TT]ATATCTTAATAGACA | 10477 |
rs760533613 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036287 | GTCAGTTGATTTTCA[A/G]CAGAAATGCCAAGGT | 10477 |
rs760566618 | snp | G/T | 1.67809e-05 | 0.00289658 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060658 | TTTTTAATGTGACTG[G/T]GCTTAGGTTACTTTC | 10477 |
rs760574220 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005764 | AGCTTTAATCTTTTG[C/T]ATATGTATTTAATAT | 10477 |
rs760700986 | snp | A/C | 0.000184262 | 0.00959673 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982119 | ATGCGGACCAGCGAG[A/C]CCCAGCCGCTCCAGA | 10477 |
rs760705050 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003249 | GTTATTTGTTATGAG[C/T]TTAATTTTTTTATAT | 10477 |
rs760739903 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043619 | AACCTGAATTATTGT[A/G]TAATATTTGATAAGA | 10477 |
rs760749336 | snp | A/T | 1.70635e-05 | 0.00292087 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982264 | AGAAGGATCCAGCAC[A/T]CTTTGTCAGGTTGTC | 10477 |
rs760796812 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016807 | AAATAAGAACAAAAC[-/TT]TTAACAAAAAATTGG | 10477 |
rs760827047 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044472 | GGAAAAAAAGAATCT[G/T]TAGTGGCAATAGAGA | 10477 |
rs760860655 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056043 | AAAAATGTTTGATTC[C/T]AAGGATGGGATTCCT | 10477 |
rs760870894 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026689 | TATGAGATTTGTTCC[A/G]CCATTACTTCAGGTA | 10477 |
rs760936578 | in-del | -/TT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061109 | TGCACAGACCACTTC[-/TT]TTTTTTTTTTTTTTT | 10477 |
rs760955348 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014798 | ATGTATAATGATCAA[A/T]TGGGGATAATTGGGA | 10477 |
rs760978332 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009376 | CACCAAAATAAAAAA[C/T]GCAGTTTTTACCCAT | 10477 |
rs761013225 | snp | C/T | 1.67911e-05 | 0.00289746 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181062816 | GGTTGGAAGCATAGC[C/T]ACTCAGTATTTGACC | 10477 |
rs761037583 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013663 | GAATATTCTGAAGCA[G/T]GGGAAGTGGGAAGAA | 10477 |
rs761057870 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043346 | AACCAGATTGTCCAC[-/AT]GAGTGGCTGAGATAC | 10477 |
rs761098531 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051215 | GTTTAATCCTTCAGC[G/T]TAACTTTTTTCACTC | 10477 |
rs761159493 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035235 | TAAAACCTACACCTA[C/T]TATACTATGATTTGC | 10477 |
rs761240747 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983052 | TGAGACTCTTATCAG[C/T]GGTAGTAGTAGTGGA | 10477 |
rs761257240 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062177 | AGGAAGGAAGATAGT[G/T]TTTTTTTACTGGCTA | 10477 |
rs761273082 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011752 | GTGTTATAGAAATTG[G/T]ATCATACCATTATTT | 10477 |
rs761330179 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993637 | AAACACTGTTTATTC[C/T]CTTTCTGAGGATGGT | 10477 |
rs761414629 | snp | C/T | 1.67461e-05 | 0.00289357 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057855 | GTGCATTCTTTAGTA[C/T]TTAATCCTTCTCCTC | 10477 |
rs761432543 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999117 | CTAAATGACAGTTAT[C/G]TAATCTCACTGATGA | 10477 |
rs761460090 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005624 | AACTAATTTATATTA[C/G]CTGTGTGGCACCTTA | 10477 |
rs761466107 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051656 | TTATTTTGGTGATAT[G/T]AATAGTGATTGATTT | 10477 |
rs761486126 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038265 | ACAGTTGCCTACAGT[A/T]TTCTATATAATAACA | 10477 |
rs761529878 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998101 | AACTTGCCAGACTCA[A/C]AGTGTAGAGCACAAC | 10477 |
rs761584455 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022137 | AACTTTGATGTCCTA[C/T]GATTAATATTGTTAT | 10477 |
rs761608503 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994175 | CCACATTTCCATTAG[A/T]AGATGCCAAATACTC | 10477 |
rs761630923 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018200 | AAAAACAGTTATACT[A/C]TAGTAGCAATTTATG | 10477 |
rs761668070 | in-del | -/TTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031513 | TTACTCTGTGTGTTT[-/TTA]TTTATTTAGTCTGAC | 10477 |
rs761670558 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057077 | TAATGTTATAAAAGT[C/T]AAAGAAAGGCGGAAA | 10477 |
rs761675963 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002875 | GAACTGGGGCACACC[C/G]CAGTTTGTGAAAAGA | 10477 |
rs761699908 | in-del | -/GATT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984146 | GGAAAAATACCAAGA[-/GATT]GATGTATTGTCTGGA | 10477 |
rs761708723 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053707 | TTAACACATCATTAT[C/T]ATGCAAAGTCCCTAG | 10477 |
rs761720411 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017083 | AAGAGAAAACTGGAG[C/G]TGGAGACAGAATTGG | 10477 |
rs761740523 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023788 | AATGACGATGATAAA[A/T]TATCTACCTGATAAT | 10477 |
rs761776023 | snp | C/T | 3.43773e-05 | 0.00414577 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982275 | GCACACTTTGTCAGG[C/T]TGTCTTCCAGGTGGT | 10477 |
rs761804054 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044968 | TTTAAAGTCAGAGAA[C/T]TTACTAAGTGTTTAC | 10477 |
rs761808316 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028527 | CACCAGCAAAGTGCA[A/G]TAGTTCTCTTTGCGC | 10477 |
rs761826588 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990469 | ATCCTTAATATATTC[A/G]CCTACACCTTCCTCA | 10477 |
rs761832251 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001813 | TGGATGCAGTTCACC[C/T]TTCATATCTGTTAAT | 10477 |
rs761859501 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042001 | GTAAATGAGGATATA[A/G]TTGTGGAGCCTTCTG | 10477 |
rs761899630 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055140 | AGTTCAAGTAACAAC[A/G]GAGGAGAGAAACTGA | 10477 |
rs761906682 | snp | C/T | 1.73972e-05 | 0.00294929 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984117 | TGAATTTTGTTGTTT[C/T]GGTTTCAAATTGTGG | 10477 |
rs761918691 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984691 | TTTTGGTGGTTGGAA[C/T]ATGTGTATGAAAAGC | 10477 |
rs761926213 | snp | A/G | | | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987363 | TGTCCTCTCCTAGTC[A/G]CCACTTGTGCAAACA | 10477 |
rs762010025 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036999 | TGATTGTGACCTCAC[A/T]TCATCCATAGTTATG | 10477 |
rs762014728 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013523 | GTTGGCCTACCTGTA[A/G]GCTGCTTAAGTGTTC | 10477 |
rs762089645 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020471 | GGGGTTAGAACTTCA[A/G]CATTATCTTTTAGGG | 10477 |
rs762108634 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012515 | GGTTTGTGAGTGTAA[C/T]TGATTTTAAGTCATT | 10477 |
rs762132615 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993119 | GTTTTATAAGGGTGT[A/G]TAGAGAAATAACAAA | 10477 |
rs762194273 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024594 | ATGTAATGGTGATGT[A/G]CTATGTAGATATGAA | 10477 |
rs762209690 | in-del | -/TG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018361 | TAATATTTTTATCTC[-/TG]TGTGTGTGTATATAT | 10477 |
rs762213923 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979804 | AGACAGAAGAGTCCC[A/G]CAGAAAAGTGTCATG | 10477 |
rs762228962 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045110 | ATACAGCAGGAAGAG[C/G]TGAGAATCTTAAACT | 10477 |
rs762238456 | in-del | -/AT | 3.36814e-05 | 0.0041036 | utr-variant-5-prime, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982029 | AAAGTTTTCCAAGAG[-/AT]AACTTCACCAAGATG | 10477 |
rs762260879 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032021 | ATTCTGCAATGGAAA[A/G]CCAGCTTCAGGGAGG | 10477 |
rs762263031 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984224 | GCAAGTGCATTAAAC[-/A]AAAATTGTAGAAGGT | 10477 |
rs762349172 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049986 | ATATATGAAATGAAG[A/G]CTAGATTTCAAAAAT | 10477 |
rs762362049 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060226 | CTGAATTGATACTGA[A/T]CTTTTCTAGTAAGAA | 10477 |
rs762373201 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043292 | ATGCTTACTAGTAGC[A/G]TATAAATTCAAGAGT | 10477 |
rs762403734 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995461 | TGTAACATACAAAAC[A/G]TTTCTGTTATTGGTA | 10477 |
rs762423529 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042614 | AACAGGTTAGAATTC[A/C]GGTTCTGCCACGTAT | 10477 |
rs762628346 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048823 | TTTACTTTAGAAAAA[G/T]ATTACAGAAGCTACC | 10477 |
rs762683583 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060020 | TTTCTCACACATTTC[A/C]GGGATATATTAGTTT | 10477 |
rs762754920 | snp | A/G | 1.78315e-05 | 0.00298587 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984133 | GGTTTCAAATTGTGG[A/G]AAAATACCAAGAGAT | 10477 |
rs762760035 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019397 | TAACCTTGCATTAAT[A/C]TTTTTTCTACCTGTA | 10477 |
rs762765973 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023463 | TAAAATTAATGCTTT[-/C]CACCTTTCATTTGAT | 10477 |
rs762794537 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056437 | CCTCAGGCTGCTTCA[A/G]CTCACAGTGGAAAGG | 10477 |
rs762798493 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988629 | GCTGTTACCTGCATT[A/C]CCTAACCCCATAGCA | 10477 |
rs762806721 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015016 | AGCCCTTAAGATGTG[C/T]GGTCAAGCAGGCATT | 10477 |
rs762827948 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027127 | TCTTAGATTGTCTGT[A/G]CCTGTGTTAAAATGT | 10477 |
rs762866400 | snp | A/G | 0.000124665 | 0.00789411 | intron-variant, synonymous-codon, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989963 | AGTCTCTTCTTCCCT[A/G]TCAATATGAGATAAA | 10477 |
rs762947483 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998888 | AACCATAATTAACTA[C/G]GTTGTTTGTAAAATA | 10477 |
rs762977894 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039185 | GAACGAGGAAACATT[G/T]TTGGGGTGGTGGATA | 10477 |
rs762992286 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053498 | CTCTTATTTTAATAT[A/G]TAAATATTTGCTTGT | 10477 |
rs763036257 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023730 | ACTTACCAGATGTGT[A/G]GCTTTAGGTTCATTA | 10477 |
rs763065824 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040469 | TTTTGCCACAGTGCA[-/T]TTTTTTCATGGTTGA | 10477 |
rs763100307 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024461 | ATGGAGTAAACAAGC[A/G]ATAAGCAGATTAGGT | 10477 |
rs763158944 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978690 | ATTGAAATAACTTAA[C/T]TTGCCTGAGGTCATA | 10477 |
rs763174502 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059868 | GATTCAACTTTTGCG[C/T]TCACAGTACACTGCT | 10477 |
rs763204892 | in-del | -/A | 3.37598e-05 | 0.00410838 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982245 | TAAAAGGTAATGTGT[-/A]AAAAGAAGGATCCAG | 10477 |
rs763217092 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036256 | AGGAGCCCAGAAGTA[A/G]ATCCACACATAAATG | 10477 |
rs763218010 | in-del | -/AG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015638 | ATTTTTTATAATAAC[-/AG]ATAAGGATGGAATAA | 10477 |
rs763234551 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992398 | AGTGCAATTAGACTA[C/T]AAAAGGAGATGTTAA | 10477 |
rs763238421 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031063 | TTTAGCTTTTCTTCT[G/T]TAATACAAACATTAA | 10477 |
rs763266111 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007899 | TGTATAAATAGCCAC[A/C]GCTAACATTTAATGA | 10477 |
rs763288247 | in-del | -/TTTTTCCCTGACAGTTTATGTTAAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025405 | GAAGATATTATCTAT[-/TTTTTCCCTGACAGTTTATGTTAAA]ATACATTTAGCTTTG | 10477 |
rs763346217 | snp | C/G | 3.34835e-05 | 0.00409153 | utr-variant-5-prime, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982039 | AAGAGATAACTTCAC[C/G]AAGATGTCCAGTGAT | 10477 |
rs763377956 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039283 | TCAAAATGGTGAATA[-/A]ATTTTATAAATAAAT | 10477 |
rs763423755 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001772 | TGGGTAACAAATTGG[A/G]GAGGGCGGAGAGAAA | 10477 |
rs763509746 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054883 | TTAGGGTGATAAGGA[A/G]TAGGAATAGAGAGTG | 10477 |
rs763568970 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026206 | ATTTTGAAAATAATG[A/G]TTGAAGCTAATACTT | 10477 |
rs763571027 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038150 | AGTCCTGAAAGCTCC[A/G]TTGTGGTAAGTGCCC | 10477 |
rs763671242 | snp | A/G | 1.67329e-05 | 0.00289243 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057852 | GAAGTGCATTCTTTA[A/G]TATTTAATCCTTCTC | 10477 |
rs763687652 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997875 | ATCTTTTTGTGAAGC[C/T]CTTCCTGCACATATC | 10477 |
rs763706762 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992278 | AATCATTCCATTCAT[G/T]CTAGATACACAGTAT | 10477 |
rs763784770 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996583 | ACATTGAACATCCTC[-/A]AGACTCTGCTGACTA | 10477 |
rs763799420 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979731 | AGCTTTTCTGGGTGG[A/G]CATTCTGACTCAACA | 10477 |
rs763859480 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007073 | TCTTTCATCTCCCAG[G/T]CCTTCAAAGTTCTTC | 10477 |
rs763865706 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983726 | TTGCATATAAGCTTG[A/G]AAAGAGAATTTCTTT | 10477 |
rs763876546 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015184 | AAGGGTGGAATCCTA[C/T]ACATGTGAATTTAGT | 10477 |
rs763927163 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044746 | CTAAAGTCCCTGTGA[A/G]TGGTTCTTACATTAA | 10477 |
rs763938781 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048319 | TTCCTAGCCCCAAAT[C/T]GTAGACACTCAATAA | 10477 |
rs764023860 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040716 | TTTAGTCTGATGACA[A/G]AGGAAATCACTTTTT | 10477 |
rs764033112 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038987 | AGGCAAAATGGTATG[C/G]CCACTTGGGATAACA | 10477 |
rs764050671 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027186 | CTATTTTATGACTTA[C/T]GTGAATTTCGGATTT | 10477 |
rs764051704 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043726 | TCTTTTAAAATACAC[A/G]TACTGTATACACATA | 10477 |
rs764051809 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057024 | CTCAAAATGATGAGC[A/G]TTTTTTAAAAAAGAA | 10477 |
rs764078954 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012341 | ATTGGTTAGTTACAG[G/T]TGTCATTTGAATCAG | 10477 |
rs764104808 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056320 | GTTCTAGAATTGGAA[A/G]ATCATGATTTTATTG | 10477 |
rs764128145 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988638 | TGCATTACCTAACCC[C/G]ATAGCATTCTTTCCA | 10477 |
rs764133705 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998050 | AGCACTAACTATGAG[A/T]ATAATTTTAATTAAC | 10477 |
rs764134539 | snp | C/T | 1.70848e-05 | 0.00292269 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982265 | GAAGGATCCAGCACA[C/T]TTTGTCAGGTTGTCT | 10477 |
rs764163182 | snp | G/T | 1.67843e-05 | 0.00289687 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060825 | CTGGTAAGCAAATCT[G/T]TATTAACATGTACAA | 10477 |
rs764196397 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988900 | GTCCTTTTATTTTCA[A/G]TTCTTCAAAAAAAAA | 10477 |
rs764328087 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986084 | CTCATTTAGTGATCA[G/T]ACTAGTGAAACATCA | 10477 |
rs764414337 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994985 | TAACTATAACATACT[C/G]TATTACTGCAGTAAT | 10477 |
rs764440297 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023823 | GTGTGAGAATTAAAT[G/T]AATTGATACATGGAA | 10477 |
rs764453916 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992406 | TAGACTATAAAAGGA[C/G]ATGTTAAATTTTTCT | 10477 |
rs764512789 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030408 | GTGTATATTTTTCTA[A/C]TGTCAGACTAACTTT | 10477 |
rs764521744 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019416 | TTTCTACCTGTAATA[C/T]AAACTTTTAAACTTT | 10477 |
rs764540099 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991616 | ACACAAACTCATAAA[C/G]TTTCTTAAAACATGA | 10477 |
rs764541701 | in-del | -/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992227 | TGTTCTTTGTTTACT[-/G]GGTTGTTTTTCCACT | 10477 |
rs764550655 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042375 | GTTAGCCCCCCATCA[-/G]TGTGACCTAATCAAA | 10477 |
rs764577639 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031086 | AACATTAAAGCTGTA[C/T]ATTTACCTCTAAGTA | 10477 |
rs764579923 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059152 | GTTCACTCTGTTGCT[C/G]AGATATACAGTATTA | 10477 |
rs764585793 | snp | A/G | 1.67329e-05 | 0.00289243 | missense | UBE2E3 | GRCh38.p7 | 2:181062838 | TATTTGACCAACAGA[A/G]CAGAACACGACAGGA | 10477 |
rs764607724 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018962 | CTTAAGTTCCTTTCT[A/G]GCTCTAAATTTTTTT | 10477 |
rs764617613 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041933 | GACCTTAGTACTGTT[G/T]ACTATAAACATTATT | 10477 |
rs764701283 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007461 | TCCGGAAAAGAAGAG[-/T]AAAGTGGAGATAAGT | 10477 |
rs764717369 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993687 | CATTTACAGTCTTAT[A/G]GGTCCTTTACAAATG | 10477 |
rs764737018 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034552 | GGAGCGGGGAGAGAT[A/G]GCATTAGGAGATACA | 10477 |
rs764739808 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039055 | ATGTGACTCAGTGTT[-/A]ACTGGTTAAATTACA | 10477 |
rs764748848 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041128 | CAGCACGTGCCTGTA[G/T]TCCCAGCTACTTGGG | 10477 |
rs764751320 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978552 | AGATCCTAAATATTC[C/T]GTTGGGTGAATGTTA | 10477 |
rs764762335 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047690 | TTCTTTGTCTCTGGT[A/G]CCATATTAGTCTAGC | 10477 |
rs764792875 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013620 | GTAACCTGGACTTCT[A/G]TAAACCTGATGACTG | 10477 |
rs764816794 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059055 | TGTATATGATTTGCC[A/G]TAATTTTGATGAATA | 10477 |
rs764875130 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011945 | GGTTGTTAGGCAAAA[C/T]GGACTCCATAGAGTG | 10477 |
rs764880315 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042313 | GTGCCTTCAGAGGCT[A/G]TTTACATGTTTAAAG | 10477 |
rs764889230 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181046490 | TATCAACTGTTAGTT[A/G]TATTTTACCTAATCA | 10477 |
rs764920625 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019320 | GATAGACGCTAAATC[A/G]TTGGAACATGTTCAG | 10477 |
rs764935556 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053863 | TTCATCCCTTCCACC[A/C]CACTAACCCCTGGCA | 10477 |
rs764997022 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026033 | AGAAGCAATTTGATC[C/T]CATTTGCAGGGTCAA | 10477 |
rs765026384 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984749 | CATTTTAGTGGAACT[C/T]AGGTAGATGAATTTA | 10477 |
rs765051018 | in-del | -/AAATGCCATTTTGG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031956 | GTTTGTCCGGCTCAC[-/AAATGCCATTTTGG]AAATGCCATTTTGGA | 10477 |
rs765228052 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036944 | GCAGTTTCCAAGAAC[C/T]TATCCACAACATTAA | 10477 |
rs765253413 | in-del | -/GT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001640 | CTGTCAAAACTGAAG[-/GT]GTAAGGATTCTTACA | 10477 |
rs765253453 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025035 | TTTTTAGAATTCACT[A/G]TAAGCCTTTCATGTG | 10477 |
rs765268650 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009709 | ACTTCTACTTAAGTG[A/G]TAATTGTGACAATTT | 10477 |
rs765405539 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057157 | GACTGGGTCCTGCAT[C/T]GGAGAAAAATTAATT | 10477 |
rs765424700 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984950 | TGCTCAATAATGCGA[C/G]TGGCTGCAAGGAATT | 10477 |
rs765493897 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058421 | GAGAACGGGGTGAGT[C/T]GTGCCTTCTAATGAC | 10477 |
rs765520110 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993980 | ATTTACCTGGTATCA[C/G]AATGAGAAGAAACCT | 10477 |
rs765566160 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058415 | ATAACAGAGAACGGG[G/T]TGAGTTGTGCCTTCT | 10477 |
rs765569428 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001525 | GGGATGGATTGATAC[A/G]GCACCAGATAAGTAG | 10477 |
rs765597986 | in-del | -/CCT | 1.65872e-05 | 0.00287981 | cds-indel, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982124 | ACCAGCGAGACCCAG[-/CCT]CCGCTCCAGAGCCTG | 10477 |
rs765683012 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004843 | CTTTATTGTTTCTTG[A/G]CCTTTTGCCAAATGT | 10477 |
rs765760267 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029073 | ATAACTATTTGTTTT[A/G]GTAACTTTATTGAAT | 10477 |
rs765772162 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042615 | ACAGGTTAGAATTCA[C/G]GTTCTGCCACGTATT | 10477 |
rs765814022 | in-del | -/AG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045068 | GCTTTATAAGCAGAA[-/AG]AGAGGGAGGGAAATG | 10477 |
rs765837336 | in-del | -/AAAGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032240 | CATTATTTCAAAGGA[-/AAAGT]AAAATAGAATATGGT | 10477 |
rs765865836 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045183 | CTTGTGCTGTGTATG[A/G]GTAAGAAGGTTGTAG | 10477 |
rs765889986 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017561 | CACCTCATGGAAATG[C/T]GGTAATATGCATACC | 10477 |
rs765908336 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990549 | ATATTATTTGTCATA[C/T]GTGTGTGTTATTTTT | 10477 |
rs765992960 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057158 | ACTGGGTCCTGCATC[A/G]GAGAAAAATTAATTT | 10477 |
rs766002175 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030211 | CTCTTCATTGGGCAT[C/T]AAATTTTAATGAATA | 10477 |
rs766022849 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053920 | AGTTTTGCCTCCAGA[A/G]TGTCATATAGATGGA | 10477 |
rs766092017 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996108 | TATAGAATTTCTTAA[-/T]TTAAAAAAAACTTCA | 10477 |
rs766100198 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986304 | ATAAGTGGTTTCTTA[C/T]TATTTGGAGGCAGTG | 10477 |
rs766145547 | snp | A/G | 1.78806e-05 | 0.00298998 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984135 | TTTCAAATTGTGGAA[A/G]AATACCAAGAGATTG | 10477 |
rs766195642 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012169 | ACATTTTTTAATAGT[A/G]TTCATGTTCCTTTCT | 10477 |
rs766249995 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024698 | TTTAGTGACTACTTA[C/T]ATGCTCATCATCTAG | 10477 |
rs766263574 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995098 | TCTGTATAAACAGTT[C/T]ATCACTCCAGTAAAT | 10477 |
rs766302753 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062226 | ATATTGTACCATATG[C/T]ACATATTTTTTTGTT | 10477 |
rs766341744 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034548 | GGGGGGAGCGGGGAG[A/G]GATAGCATTAGGAGA | 10477 |
rs766418781 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020579 | CTTTGTTTTTAATTC[A/G]TAGTCATTTCAATAA | 10477 |
rs766445460 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019783 | AAATAATCACCATAA[G/T]CTAGTTAACGTAGCC | 10477 |
rs766485985 | in-del | -/TGTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018597 | TTGTTTCAATTTCTG[-/TGTTT]TTTTTTTTTTTTTTT | 10477 |
rs766498989 | in-del | -/ATT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022416 | TAGGGGAAATAAAAG[-/ATT]ATCTTTTTTTGATCT | 10477 |
rs766555601 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993473 | GACATCTCTAGTCCA[A/G]AATTGCTTTTGGGAG | 10477 |
rs766566296 | in-del | -/TCTCT | 1.7212e-05 | 0.00293355 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984021 | ATCAAATCCTTTTTG[-/TCTCT]TCTCATTTCACTAAC | 10477 |
rs766607564 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039219 | TCTATATCATGGTTG[C/T]AGTGATGTTACAGGA | 10477 |
rs766643480 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992615 | ATCCTCCCACCTCAG[A/C]CTTCCGAGTAGCTGG | 10477 |
rs766645204 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014913 | TTAACTATAATTTCC[C/T]ACTGTATTATTGAAG | 10477 |
rs766729063 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001903 | AATGGCAAGACTGTC[-/T]TTTACTATTAAGTAT | 10477 |
rs766732343 | snp | C/T | 3.35351e-05 | 0.00409468 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057860 | TTCTTTAGTATTTAA[C/T]CCTTCTCCTCTAAAA | 10477 |
rs766734593 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047925 | AAGGTCCTGCCTAGA[C/T]GTTTGTTACAGCTTC | 10477 |
rs766835911 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983060 | TTATCAGTGGTAGTA[C/G]TAGTGGAATATCCAC | 10477 |
rs766864022 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984851 | TTCATTTGTATAGCG[C/T]TCTATTCTTTTTTTA | 10477 |
rs766897393 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022255 | TAGACTCTTGAAAAT[A/G]AGATTAGTATTATTG | 10477 |
rs766995325 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027283 | GATGGACCTCAACAA[A/G]TGTGGGAAAGTGTTA | 10477 |
rs767014526 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050319 | AAAACTTGAATTTTA[C/T]ATCATTTTGTTTTTC | 10477 |
rs767125889 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009317 | TATAAAACCAACTTT[C/G]AATTACTAAATTATC | 10477 |
rs767147494 | snp | A/G | 0.000130014 | 0.00806163 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989839 | CTTTATGCTCTCCTT[A/G]AATGAGTTGCTGTAA | 10477 |
rs767199785 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994216 | TTTGAAAACCCTAAA[A/C]TAAGCACGTTGCAAT | 10477 |
rs767208429 | in-del | -/AT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048241 | TTGTGAGTTTATTTG[-/AT]ATTAAGATCTATATC | 10477 |
rs767210651 | snp | A/C/G | 0.0006599 | 0.0181547 | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989992 | AAAACATAATAAAAT[A/C/G]ACTTGTAAATCTAGA | 10477 |
rs767235440 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988738 | AATAACATGTGATCC[C/T]TATATTAGCTTTGTT | 10477 |
rs767308821 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999569 | CGTATGAGGGTTCCA[A/G]TTTGTCCACATCCTT | 10477 |
rs767329562 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998125 | GCACAACAGCAACTG[C/T]GCTTGACCGTACTCC | 10477 |
rs767335864 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996174 | TAAAAGTCATATGGA[C/T]CTATTTGGTGTATAA | 10477 |
rs767381314 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989821 | TCTCATAACCAATTA[A/G]TACTTTATGCTCTCC | 10477 |
rs767415082 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016367 | TTACAGGCATGAGCC[A/T]CCATGCTTGGCTAAT | 10477 |
rs767422120 | in-del | -/AGAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058016 | TAATTTGTAATAAAC[-/AGAA]AGAGTTTAATTCTTA | 10477 |
rs767434490 | in-del | -/ATA | 0.000108619 | 0.00736869 | intron-variant, cds-indel | UBE2E3 | GRCh38.p7 | 2:180989982 | ATATGAGATAAAAAC[-/ATA]ATAAAATCACTTGTA | 10477 |
rs767467979 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017117 | AGGAATGCAACCTGT[A/G]TTATAGAAGGGCCTG | 10477 |
rs767481831 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002894 | TTTGTGAAAAGATGG[A/G]CAACCTTTCTTGGCT | 10477 |
rs767513977 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045046 | TGTTTATGCTTTTAC[A/G]TCTGCTGCTTTATAA | 10477 |
rs767514029 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036591 | AGTGAGTGAGGGGGT[G/T]TGGGGGTTATGTGAA | 10477 |
rs767547667 | in-del | -/AGTCC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016284 | AGGATCTCACTGTGT[-/AGTCC]AGGCTGGTCTTGATC | 10477 |
rs767570022 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043316 | CAAGAGTAAGGAATG[A/G]TGGTGATGCCAGTCA | 10477 |
rs767598762 | in-del | -/TTAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058125 | ACCTTCATTAATACC[-/TTAA]TTAATAATACCTTAA | 10477 |
rs767620209 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991847 | GCAGGGCAATGTGAG[A/G]TTTCATCGTGCTACT | 10477 |
rs767623298 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042009 | GGATATAATTGTGGA[A/G]CCTTCTGCATTTGTC | 10477 |
rs767822625 | snp | A/G | | | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:180987439 | TCTTTCCATATAGGA[A/G]GAAGCACAAATATAC | 10477 |
rs767846679 | snp | A/G | 1.65886e-05 | 0.00287993 | missense | UBE2E3 | GRCh38.p7 | 2:181060767 | GCTTTGACTATTTCA[A/G]AGGTTTTGCTGTCTA | 10477 |
rs767860387 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031424 | GGCTATTTTATTATG[C/T]AGAGCAAGCTTACAA | 10477 |
rs767875487 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012650 | CTGAGTAAAATGAGT[A/G]CAGTATATTCTGTGT | 10477 |
rs767883355 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982704 | TGCTATATTTGAAAG[C/T]AGATTTAAAATTGTG | 10477 |
rs767914795 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062214 | GGTACAATTCAAATA[C/T]TGTACCATATGTACA | 10477 |
rs767934836 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050184 | AATACTCTGATCACT[A/G]TTTCCTGAACAGTTA | 10477 |
rs767942113 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019547 | GAATAATAGAAACTA[A/G]AAAACTCAGGAGATG | 10477 |
rs767973313 | snp | A/G | 1.6898e-05 | 0.00290667 | missense | UBE2E3 | GRCh38.p7 | 2:181062806 | CGGATCCTCTGGTTG[A/G]AAGCATAGCCACTCA | 10477 |
rs768010993 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020481 | CTTCAACATTATCTT[G/T]TAGGGGCCTACAATT | 10477 |
rs768038215 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022867 | AAATGACTGCAAAAG[C/T]CCCTAGTATTGATTT | 10477 |
rs768044840 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181032103 | GAGGTTTTCATTCCC[C/T]GAAGAAGCAAAAGTT | 10477 |
rs768058829 | snp | A/C | 1.65809e-05 | 0.00287926 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982175 | CCTTCTGCCACCCAG[A/C]AGAAGAAAAACACCA | 10477 |
rs768063636 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062078 | TCTAAATGCTTGTCA[A/G]TGCATGTAAGAACTC | 10477 |
rs768116985 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060245 | TTCTAGTAAGAAACT[A/G]ATGTAACTTTTATGT | 10477 |
rs768125584 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013134 | GGCTGACTACATTAA[-/T]TTTTTTAAATTGCAA | 10477 |
rs768183946 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984417 | CTTCTAAAATTTTGC[G/T]AAGCTTTAAAGTTAC | 10477 |
rs768217919 | snp | C/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020459 | TTTGAGATACTGGGG[C/G/T]TTAGAACTTCAACAT | 10477 |
rs768270285 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009192 | TTAGTAATTGTTAAT[A/G]TAATGCTAGAGTGAT | 10477 |
rs768273939 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982410 | TAAGCAACATTACTA[C/G]AATTATACTTTTAAG | 10477 |
rs768323265 | snp | G/T | 7.07026e-05 | 0.00594528 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062890 | GATACGCAACATAAT[G/T]CACATAATTTGTATG | 10477 |
rs768324241 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021735 | TGGTCATGGAACCAT[A/G]TAAAGTAATTTAGCA | 10477 |
rs768341505 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988412 | TCAGGCATAGATGAA[C/G]AAATATTGTATTCCT | 10477 |
rs768361704 | snp | C/T | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180993087 | TTGGGATTTTTATCT[C/T]TGTTGACATTCTATC | 10477 |
rs768377057 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034187 | ACTGGGTATATACCC[A/T]AAGGATTATAAATCA | 10477 |
rs768380629 | snp | C/T | 3.33089e-05 | 0.00408085 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181060670 | CTGTGCTTAGGTTAC[C/T]TTCCGCACCAGAATC | 10477 |
rs768507167 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038965 | CTCTCATACATTACC[A/G]TTGAGAAGGCAAAAT | 10477 |
rs768517056 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057643 | GTTTTAGGATATTAA[C/T]ATTCATTGCTAATAT | 10477 |
rs768521386 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028195 | AATGTAATTATACTT[G/T]TTTCTCTTAAATCTT | 10477 |
rs768538458 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024101 | GGTCAGGTAAACATG[A/T]ATGTTCAGTCCTTCA | 10477 |
rs768581259 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040008 | TGGTTGAATCTGTGT[A/G]TGTAGAACCCATGGG | 10477 |
rs768588319 | snp | G/T | 0.00146306 | 0.0270072 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060863 | ACAAAAACGAGTGCT[G/T]TTTTTTTTTTTTTTT | 10477 |
rs768612845 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001440 | CCTCCACCCCCCACA[C/G]CCCCAACTGTGAATG | 10477 |
rs768666780 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055022 | ACCAGTCAAATAATA[C/T]GAAGATTGAGAAATG | 10477 |
rs768668261 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999762 | TCTTGGCTTTACAAT[A/T]GAGTAACTGTAAAAG | 10477 |
rs768682553 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029654 | GATTTTTATCTGTAG[A/G]CAATCTTTTTTTTTT | 10477 |
rs768742587 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978782 | TTCTGTAGAAGATGT[C/T]ACCAAACAACTAAAT | 10477 |
rs768747088 | snp | A/C | 1.70874e-05 | 0.00292291 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984101 | AATTGCAGGTAAGAA[A/C]TGAATTTTGTTGTTT | 10477 |
rs768757959 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999000 | AGTGGTATAAATGTC[C/T]CATGTGTCTTTTATT | 10477 |
rs768870166 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031987 | AATGCCATGTAGCCT[C/G]TTCTTACAATCTAAG | 10477 |
rs768906090 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006571 | AATATTAGGAACATG[C/G]TAAATATTTCTCGTT | 10477 |
rs768917081 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003476 | TTCCAGGGGGGATGA[C/T]GCTGTCTCAAGATTT | 10477 |
rs768943930 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036912 | TGGTTTCAGTATATG[G/T]CATTTCACATAAAGT | 10477 |
rs768952785 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015013 | AGCAGCCCTTAAGAT[A/G]TGTGGTCAAGCAGGC | 10477 |
rs768968330 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997243 | GCTTCCCATTTATCT[A/G]TCTCTATTTATTTTT | 10477 |
rs768980771 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030769 | TGTATAACCAGTATT[-/C]ACTTAGTCTGTTCTT | 10477 |
rs769003790 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181044350 | AAAATAGGATGAAAT[A/C]TCTAAGCGATAAATA | 10477 |
rs769004851 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014628 | GGTAGAAAGTATTTC[A/G]TAGGTGTGCCAGGTA | 10477 |
rs769131649 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060965 | GTTTGTGAGGAAATT[A/G]CCAATGCCATTTGAA | 10477 |
rs769160261 | snp | C/T | 1.76067e-05 | 0.00296699 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062788 | TTCTTTCTGCTTTTC[C/T]AGCGGATCCTCTGGT | 10477 |
rs769231874 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015818 | CATGGTCCTTGTTCC[A/T]TATACTAGAGATGAT | 10477 |
rs769263840 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988410 | CTTCAGGCATAGATG[A/G]ACAAATATTGTATTC | 10477 |
rs769294490 | in-del | -/TGTTGGCAAATGGCCCTAGTTTCTTGACT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013477 | CAGTTCCTCACTGGC[lengthTooLong]TGTTGGCAAATGGCC | 10477 |
rs769424254 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020376 | AGATTAAGGGCCACC[A/G]TACTCTGGTATAACC | 10477 |
rs769435613 | snp | G/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992244 | GTTGTTTTTCCACTT[G/T]GCTTTCAAATACTCT | 10477 |
rs769512271 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031907 | TTCCAGACTAGTGAC[C/T]TTTAAAATGCCAGTT | 10477 |
rs769560838 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026295 | TATTCTGTAGATTGT[A/C]ATGGCATTTTTTTGT | 10477 |
rs769598915 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057644 | TTTTAGGATATTAAC[A/C]TTCATTGCTAATATA | 10477 |
rs769628606 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050897 | TGCTTTGAAACTTCC[A/T]TCTTTCTTGTTTCAA | 10477 |
rs769632359 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038008 | AGCTAAAGTTAATTT[A/T]TTATTGTGGAAGAAA | 10477 |
rs769640346 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998734 | TGCAAACAGCTGAAA[A/G]TAGAAGTAAATCAGA | 10477 |
rs769675700 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982377 | ACTTGAATGAGTTGT[C/G]ATTCTTTAGGTGGTA | 10477 |
rs769694052 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000220 | TCTTTAAAAAATCTA[-/T]TTAAAGTAGCTTTCT | 10477 |
rs769729004 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009074 | CATTTGTATAAAATC[A/G]TTAAAAGGTAAAGAA | 10477 |
rs769758650 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049833 | ATATAGCACGCACAC[A/C]CAGCCATTTTATTTT | 10477 |
rs769772718 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994913 | CAGACCACACATGGT[A/G]CCATTTGGAGTCAAG | 10477 |
rs769870670 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005577 | TCTATTTCTCCATAG[A/T]CCTTACCTCTTCCTA | 10477 |
rs769884485 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036163 | ACTACTTGATTCTGA[C/T]GTACTAGGTAAACAT | 10477 |
rs769984537 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991784 | GACTAGAGCATATAC[A/G]GTATGGATAAACTGG | 10477 |
rs770010024 | in-del | -/AG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055354 | GACAGTGGAAGAGAC[-/AG]AGAGTGTCGGTCAGT | 10477 |
rs770128517 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013279 | AAACATTATTATTTC[A/C]TACTTTCTGTAAGAC | 10477 |
rs770131178 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025617 | CCATCGTCCTGTGTT[A/G]CTGGACTTGTCTCAG | 10477 |
rs770175105 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030919 | TAAAAAAAATTTTAG[C/T]TTTTATTGACACTAT | 10477 |
rs770182781 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055839 | AGAGTTTAAGGCGTA[C/T]GAGTCGTCTTACCAA | 10477 |
rs770208596 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979260 | AATTGAATGAGTGTA[C/T]GTCCAGCACCTAGCA | 10477 |
rs770216653 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012250 | CATGTATAACAAAGT[A/G]TACATGTACTAGTAT | 10477 |
rs770217674 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181043897 | TGATTGATTGAAAAC[C/T]GTAAGTGATTTAACC | 10477 |
rs770257188 | in-del | -/TTT | 0.0427603 | 0.139827 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTT]TTTTTTTTTTTTTTT | 10477 |
rs770329725 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018427 | ATCTGTGTATACATA[A/T]ATATTTGGCCTAGGA | 10477 |
rs770334454 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029498 | TATTCAAGTATTGTA[C/G]ATCTTTTGCTAAATT | 10477 |
rs770354538 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024352 | TTCTACCATCCTATT[A/G]TCCACTCACCTTGTA | 10477 |
rs770354658 | in-del | -/TTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029661 | ATCTGTAGACAATCT[-/TTT]TTTTTTTTTTTTTTT | 10477 |
rs770369833 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059026 | TAATATAAGAATTTC[A/G]CACTATATAGTACTG | 10477 |
rs770384543 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999328 | TTTGGTATAGTTTAT[-/C]TCCTCACCAGTTGTG | 10477 |
rs770395602 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995958 | AGATATGTGCTTAAT[G/T]TTTTTGTCTTACCAG | 10477 |
rs770398095 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986950 | ATATAGTTATGTCTA[C/G]TACATACATACCCAG | 10477 |
rs770487758 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985883 | CATGTATTAAGTGCC[C/G]TCAGAGCAATAGCCT | 10477 |
rs770618964 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012117 | AGAGAGGGCAATATG[A/T]TCAGTCAGCAACTCC | 10477 |
rs770653412 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036446 | AACCTGATTCCTGGC[A/G]GGGGCCATTGTGTGG | 10477 |
rs770677615 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986670 | TATTGCCTGAGATCT[A/G]TGAAACCTAATACAT | 10477 |
rs770684236 | in-del | -/ATTTTTGCAATAAAGACTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015445 | TGATAGTACTTAATG[-/ATTTTTGCAATAAAGACTA]ACAAAAACAAAAAGA | 10477 |
rs770704837 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049714 | TTAGGCAGATGCCAT[A/C]GTTTTTTTACTTCAT | 10477 |
rs770712953 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001353 | TTGGATTTCGAAAGT[-/A]GAATTTTCGAGCTTC | 10477 |
rs770730845 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037048 | TGATGAACAACAGTC[C/G]TCATATATAATGGTG | 10477 |
rs770741584 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040275 | CTTCTTCGTCCTTCC[A/G]CGGGACATTGACCTG | 10477 |
rs770743061 | in-del | -/TAC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003896 | CTCTCAGGAAGATGT[-/TAC]TACTATCTTTTTAGA | 10477 |
rs770746816 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007450 | AGTAGACTGGACTCC[A/G]GAAAAGAAGAGAAAG | 10477 |
rs770793536 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019298 | CGGGTCCCTGAAATT[C/G]TTAGTTGATAGACGC | 10477 |
rs770847644 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057943 | GCTTTTCATGGATTG[A/G]TATGGAAATTTTCGC | 10477 |
rs770882839 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059716 | GTAACTAGTATATGC[A/T]GTATTGGTCAGAGCA | 10477 |
rs770899078 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033224 | CCCGCATTGCCAAGA[C/T]AATCCTAAGCCAAAA | 10477 |
rs770974389 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979483 | CACTCCCTTTGTGAA[C/G]TGCACATTCTCACAG | 10477 |
rs771011020 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031719 | CATAATTCCATTCCT[G/T]CTTTACACCCATTTT | 10477 |
rs771055554 | snp | C/T | 1.6922e-05 | 0.00290873 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060647 | TTTTCCTTCTGTTTT[C/T]AATGTGACTGTGCTT | 10477 |
rs771077505 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028143 | TTTTGAGCACTATAC[A/G]TTACATAATGTAATT | 10477 |
rs771116059 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990366 | GCTGAAGTTGAGAGA[C/T]CCTCCTATAGATATT | 10477 |
rs771117638 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004432 | GAGGTCAAGAGATCG[A/G]GACCATCCTGGCCAG | 10477 |
rs771171578 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052870 | TATCTGCTGTGAAAT[A/G]CTTGCTGGTCACTTT | 10477 |
rs771178701 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057552 | TGCACATGCAAACAC[A/G]TTGGGGCTTATTTCT | 10477 |
rs771201361 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994289 | CTTGAAACATATGCA[A/G]AAGTAAACAGGCTGG | 10477 |
rs771206505 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985824 | TGATTGTCTGCAAAT[A/G]AAACAAACTAATGTA | 10477 |
rs771213902 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989576 | TAGTTATTTCCTCCA[C/T]ACGTGCCAGTGTAGC | 10477 |
rs771245329 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033062 | AGAACATTCCATGCT[C/G]ATGGATAGGAAGAAT | 10477 |
rs771279352 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010594 | AGTTTCACAGGTAGA[A/T]ATAAAAGGAAAATAG | 10477 |
rs771307288 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056973 | TTTCAGCCAGAAATG[C/T]GTTACATGAATCAAA | 10477 |
rs771351210 | in-del | -/TTGT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982501 | TAACATTCTGACAGA[-/TTGT]TTAAGGAGTTGGCAA | 10477 |
rs771367237 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023428 | AAAACTCCATTATCA[A/G]TGATATTTGTTACAA | 10477 |
rs771419883 | snp | A/G | 1.68394e-05 | 0.00290162 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982239 | CTAGTGCTAAAAGGT[A/G]ATGTGTAAAAGAAGG | 10477 |
rs771436377 | snp | A/G | 0.000116864 | 0.0076432 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982060 | GTCCAGTGATAGGCA[A/G]AGGTCCGATGATGAG | 10477 |
rs771449231 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979428 | TCACTCAGTCTTTTC[C/T]TCTTTCCCTTAACTC | 10477 |
rs771468052 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012045 | TTTGCTCTACTGCAA[C/G]GTAGAGTGCTCAGTT | 10477 |
rs771518318 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994797 | ATTAAGAATCCACAA[A/G]ATATATGTGGATACT | 10477 |
rs771551777 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983417 | GAACTGCTTTTCTCC[C/G]CCTTAACTCAGGCCT | 10477 |
rs771603846 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005313 | GTGTGAAATAGCGTG[A/C]ATCTTGGCCCCAGTT | 10477 |
rs771734248 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985629 | CCAGCCTTCTAAATG[A/G]TGTGTCAAATCTGTA | 10477 |
rs771750033 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059569 | TTCAACATGTAATCC[A/G]TGTAAGAGTATTGTT | 10477 |
rs771755305 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052200 | AATTACAATCATTAA[G/T]GTGTAACTAATTCTC | 10477 |
rs771768518 | in-del | -/CTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031717 | CTCATAATTCCATTC[-/CTT]CTTTACACCCATTTT | 10477 |
rs771780318 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984753 | TTAGTGGAACTCAGG[C/T]AGATGAATTTAAGAT | 10477 |
rs771786544 | in-del | -/AAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039281 | TTCAAAATGGTGAAT[-/AAA]AAATTTTATAAATAA | 10477 |
rs771843775 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005686 | AATTTCCTGTTATCT[A/G]TTGAATAATTTGTTA | 10477 |
rs771845436 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019250 | CAGGTGTGAACCGCC[A/G]CACCCGGCCTAGCTC | 10477 |
rs771925934 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007594 | AATTGGAGCTGGAAC[C/T]ATTTGACCTTCCATT | 10477 |
rs771926018 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030083 | ATGATCCACCTGCTT[C/T]GGCCTCCCAAAGTGC | 10477 |
rs771927811 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059538 | AGTTAACCCAACATA[C/T]TAAAAATATTGTCAT | 10477 |
rs771935332 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018257 | ATGTTTAGAGATTCT[C/G]TCCACCTTGGAGGAA | 10477 |
rs771961070 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040085 | TAATATCTGTAGCTA[A/G]TAATTATTTTAAGTG | 10477 |
rs772016951 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007141 | AGTAGTCTGTGGTGA[C/T]TTTATTAGTGATTTC | 10477 |
rs772049549 | snp | A/G | 1.66208e-05 | 0.00288273 | missense | UBE2E3 | GRCh38.p7 | 2:181057824 | CATTTAAGCCACCAA[A/G]GGTAAGAAGCTTGAA | 10477 |
rs772101858 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999529 | TGCTTTTCACAAAAG[-/C]TGTACCATTTTACTT | 10477 |
rs772175572 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056877 | AACTTAACATCACCA[A/G]TGAGGTACAGGTAGG | 10477 |
rs772176103 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001236 | GAGTTACTACATTTA[A/G]TGTAAATTAGAGTGA | 10477 |
rs772202793 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990470 | TCCTTAATATATTCA[C/G]CTACACCTTCCTCAG | 10477 |
rs772210025 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037854 | ATGCCTGTAGTCCCA[C/G]GTGCTTGGGAGGCTG | 10477 |
rs772268068 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014766 | GAGATACATGTGATA[C/T]ATGATACCTTTATAT | 10477 |
rs772296077 | snp | A/T | 1.69585e-05 | 0.00291187 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982255 | ATGTGTAAAAGAAGG[A/T]TCCAGCACACTTTGT | 10477 |
rs772336555 | snp | A/G | 1.67683e-05 | 0.00289549 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:180984043 | TCATTTCACTAACAG[A/G]ATTCAGAAGGAGCTA | 10477 |
rs772336924 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993791 | GAAGATTGTGGCTAC[A/G]TATTTTTTATGGCTT | 10477 |
rs772404966 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034983 | AGAGAAAGGGGAAAG[A/G]CAACTAATATTTTAG | 10477 |
rs772449348 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025939 | AATTTGCACATAAAC[G/T]TGTAATCACATTTTG | 10477 |
rs772471466 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010933 | TGATTTCTTTACTAG[C/T]GAGTGTCTTGAATTA | 10477 |
rs772505904 | snp | C/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063149 | GTATTTTGTGATGTA[C/T]TAAGGATACTGGTCC | 10477 |
rs772511191 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053309 | CCTTATTTAATATTA[C/T]AGAAGAAATAGTTTA | 10477 |
rs772516860 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045610 | GACCAAGCCCCAGAC[A/T]AATACATCAGAATCT | 10477 |
rs772570448 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034100 | TAAACTAGTTCAACC[A/G]TTGTGGAAGACAGTG | 10477 |
rs772615133 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058899 | GTGCTTTACCGTGTG[G/T]TCCCATCAGCATGTA | 10477 |
rs772656501 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181000027 | ATGATCAGTGATACA[A/G]AATAAAGAATATTAA | 10477 |
rs772667192 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004371 | TGAGTGTGGTGGCTC[A/G]CACCTGTAATCCCAG | 10477 |
rs772675855 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003668 | TTTATTTGTTTGCAC[A/G]TAGTACACTGTGGAA | 10477 |
rs772687409 | in-del | -/TA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035406 | ATTTTAAAATGTATT[-/TA]TAAAAAATATGAATT | 10477 |
rs772699474 | snp | A/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988557 | TAAAATAGAAGAATT[A/T]GTGATTTTACTGTGA | 10477 |
rs772736475 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181039248 | GACTATACATTTGTC[A/C]AAACTTAGCAGTGTT | 10477 |
rs772741624 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030093 | TGCTTCGGCCTCCCA[A/C]AGTGCTGCGATTACA | 10477 |
rs772753124 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016044 | TATAAAGTTATAGGA[A/G]ATTTTAGAAAGATAA | 10477 |
rs772759888 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015878 | AATTTATAGCTAACT[A/C]TGCTGCAAGTGCCCA | 10477 |
rs772811814 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013692 | AAGAGAGGGAGCTCA[G/T]GGGTGTGTATATGTG | 10477 |
rs772827469 | snp | C/T | 1.73936e-05 | 0.00294898 | missense | UBE2E3 | GRCh38.p7 | 2:181062791 | TTTCTGCTTTTCCAG[C/T]GGATCCTCTGGTTGG | 10477 |
rs772859018 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995008 | GCAGTAATTTTGTAG[C/T]CACCTCCTGTTGCTG | 10477 |
rs772878016 | in-del | -/TCTTC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014860 | TGGTAGCATTACAGA[-/TCTTC]TCTTCGAGCTACTTT | 10477 |
rs772900320 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040250 | CCCAGTTAAGCAATT[A/T]TGATACATCCTTCTT | 10477 |
rs772950435 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019255 | GTGAACCGCCGCACC[C/T]GGCCTAGCTCTAAAA | 10477 |
rs772964436 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052229 | TCCCATTTAGTTAGG[A/T]TGTTGGTGATGTCAA | 10477 |
rs773034952 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986921 | TTTAATTAATGAAAT[A/T]TTCTTTAATTAGTAT | 10477 |
rs773074810 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036279 | CATAAATGGTCAGTT[A/G]ATTTTCAGCAGAAAT | 10477 |
rs773102363 | in-del | -/AAAG | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988375 | AGGAACTTGCGTAAA[-/AAAG]AAAATTAGCCTAAAA | 10477 |
rs773123369 | snp | A/G | 0.000123024 | 0.00784199 | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989928 | GACATTCAGATTGAG[A/G]ATGAAGAACTTGTCC | 10477 |
rs773141665 | snp | C/T | 1.75305e-05 | 0.00296056 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984123 | TTGTTGTTTTGGTTT[C/T]AAATTGTGGAAAAAT | 10477 |
rs773147623 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018276 | ACCTTGGAGGAATGC[A/G]TTCTGGTGATGTACC | 10477 |
rs773249256 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058089 | ATAAATTTTATGCTT[A/G]TGAGGGAGAAGATCC | 10477 |
rs773353876 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043447 | ATTACTTTCAGGCTT[A/G]GTGTATAAGATGTAC | 10477 |
rs773463623 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014767 | AGATACATGTGATAT[A/G]TGATACCTTTATATG | 10477 |
rs773506222 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006864 | AGATCAGTTTTTAAA[A/G]TAAGATACTACTAAA | 10477 |
rs773509013 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982842 | CAAACTGAAAAGTAG[C/T]CCTTTACAATTTGAG | 10477 |
rs773518318 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181023127 | CCTTGACTTACAGTG[C/G]GGCCGCGCCCCAATA | 10477 |
rs773526504 | in-del | -/CGGGCGCGGAAATTTGTTGCACTT | 1.65877e-05 | 0.00287986 | cds-indel, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982127 | AGCGAGACCCAGCCG[-/CGGGCGCGGAAATTTGTTGCACTT]CTCCAGAGCCTGAAG | 10477 |
rs773532556 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979344 | GAAATGTAACTTACT[C/G]TTTAGAGTTGCTATC | 10477 |
rs773595242 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984770 | GATGAATTTAAGATT[A/G]TTGGTTGGTATAAGA | 10477 |
rs773610217 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022176 | TACTATAAGTTTAGG[A/T]GTCAGACTGCCATTT | 10477 |
rs773627481 | snp | A/G | 1.6892e-05 | 0.00290615 | utr-variant-5-prime, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982025 | TTTAAAAGTTTTCCA[A/G]GAGATAACTTCACCA | 10477 |
rs773656131 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047800 | AGCAGCCTGAGGAGG[C/G]CTTGCAAAATGTCCA | 10477 |
rs773661494 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051098 | TTTGGTCCATGATTT[C/G]TGCATGTTTTCATAC | 10477 |
rs773685223 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993830 | TTTCTGTAGTCTTCT[A/T]AATTTAAACAGTAGC | 10477 |
rs773697784 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010363 | TTTTTGGGAAGGATT[-/A]TTTTTTTGAGGTCGT | 10477 |
rs773715085 | snp | G/T | | | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181063253 | ATGGCTAGGAATTAT[G/T]TCATTTGTATTAAAC | 10477 |
rs773751900 | in-del | -/CTA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025400 | CATTGAAGATATTAT[-/CTA]CTATTTTTTCCCTGA | 10477 |
rs773754439 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038236 | GTGTTTAGATACACA[A/G]ATCACATTGTTTTAC | 10477 |
rs773763463 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999225 | CATGACCGCAAAGAA[C/T]GGCAGTTCCTAGTAC | 10477 |
rs773767394 | in-del | -/TATA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018371 | ATCTCTGTGTGTGTG[-/TATA]TATATATATATATTT | 10477 |
rs773783385 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038901 | CTGACTAGAATGGTT[A/G]AAATAATTATAAAAA | 10477 |
rs773844676 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038968 | TCATACATTACCATT[A/G]AGAAGGCAAAATGGT | 10477 |
rs773889664 | in-del | -/AAA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180999329 | TGGTATAGTTTATCT[-/AAA]CCTCACCAGTTGTGA | 10477 |
rs773925023 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984450 | CTTGTGTGTGCAATC[G/T]GAACTGACCTTCCAC | 10477 |
rs773926419 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050981 | CTAGCTTGAACATTT[G/T]TTTAAAGGAAATAAA | 10477 |
rs773970173 | snp | C/T | | | intron-variant, synonymous-codon | UBE2E3 | GRCh38.p7 | 2:180987455 | GAAGCACAAATATAC[C/T]GACGAATATTTTAAG | 10477 |
rs774014321 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982607 | GAAATTGACACTTCC[A/G]GAGATTAGCAGTGCC | 10477 |
rs774064980 | snp | A/G | 0.000127722 | 0.00799029 | intron-variant, missense, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989967 | TCTTCTTCCCTATCA[A/G]TATGAGATAAAAACA | 10477 |
rs774076079 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181009235 | TCTGTAATATTTTTG[A/G]TGCTAAGAGATTGGA | 10477 |
rs774090307 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051860 | ATAATTACTATTCTC[-/T]TGTGTTTTCTAGACT | 10477 |
rs774097439 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990444 | TGTTTTCCTGTCTTA[C/T]TAGTGATGCATCCTT | 10477 |
rs774143782 | snp | A/G | 1.94467e-05 | 0.00311817 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062927 | GAAGGAGCAGAAGGC[A/G]TCTTCTCACTGTGCT | 10477 |
rs774173761 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030012 | CTAATTTTTGTATTT[A/T]TAGTAGAGACCAGGT | 10477 |
rs774173859 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017022 | ATTGAGAACTTTATA[C/T]CACAGACAGAGTAGG | 10477 |
rs774259677 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028392 | AACATGTGTTCTAGT[A/C]ATATGTGAGTAAATT | 10477 |
rs774260367 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025912 | TAAAGAGCAGGCAAT[-/G]GGATTTATGGAAATT | 10477 |
rs774295434 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036485 | TCTTCTCCCGTGTCT[C/G]TGTGGGCTTTCTCCG | 10477 |
rs774329085 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006444 | ATACTACTTCTGGAT[-/C]TAGGATGGCCAGATA | 10477 |
rs774335740 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057052 | GAAGACTAGATTCTG[C/T]AAAAAACGTTAATGT | 10477 |
rs774348011 | snp | A/G | 4.98103e-05 | 0.00499026 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181057816 | AGATTATCCATTTAA[A/G]CCACCAAAGGTAAGA | 10477 |
rs774365909 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041937 | TTAGTACTGTTGACT[A/G]TAAACATTATTGTGA | 10477 |
rs774374464 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989773 | TTATATGTTTACTTC[A/G]CAGCTACATGCTCAC | 10477 |
rs774447954 | in-del | -/TTCCTTCCTTCC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021632 | CTCTCCCTCCCTTTT[-/TTCCTTCCTTCC]TTCCTTCCTTCCTTC | 10477 |
rs774449203 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003464 | TTTTGAAGAACTTCC[-/A]AGGGGGGATGACGCT | 10477 |
rs774562193 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181010795 | AAATATTTACCTCCT[C/G]TTGTCATATCCTCCT | 10477 |
rs774574122 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180987285 | TGAGAATTGTTGACT[A/T]GAATTGTTTAGTGAT | 10477 |
rs774586256 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996239 | TCTAGGTATTATTTT[C/G]AAAACTGAATACTTA | 10477 |
rs774614150 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025862 | TGTTTTTAAAACTCT[C/G]TAAGATAGCTCTACT | 10477 |
rs774647112 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992028 | CCATGACTGAAATTA[C/G]TTACTACTCATGATG | 10477 |
rs774660619 | in-del | -/TAAT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181015986 | AGAATGAGTCCAGAG[-/TAAT]TAGCCATGAAGATTA | 10477 |
rs774704092 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036950 | TCCAAGAACCTATCC[A/G]CAACATTAAGCGAAG | 10477 |
rs774720190 | snp | G/T | 1.65767e-05 | 0.00287891 | missense | UBE2E3 | GRCh38.p7 | 2:181060752 | GACAACTGGAGTCCC[G/T]CTTTGACTATTTCAA | 10477 |
rs774726258 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002712 | GTAGTGTTAAAATAT[A/T]CACCACCTTTTAAGG | 10477 |
rs774775706 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030940 | TGACACTATTTTGTG[-/T]TTTGTGTTGTGTTTC | 10477 |
rs774784344 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062691 | ATTATATATGAAGAT[-/A]ACTGCTGAAAAATAA | 10477 |
rs774799016 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181033149 | CCATCAAGGTACCAA[C/T]GACTTTCTTCACAGA | 10477 |
rs774808809 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043186 | TCCAACATGATGCTA[C/T]GAGTTAACCTGAACA | 10477 |
rs774828344 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042143 | TAATTGTCACATCTC[-/T]TTAAGTCTACCCTAT | 10477 |
rs774898150 | snp | A/G | 1.69456e-05 | 0.00291075 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982252 | GTAATGTGTAAAAGA[A/G]GGATCCAGCACACTT | 10477 |
rs774903008 | in-del | -/AAAC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058012 | CAAATAATTTGTAAT[-/AAAC]AGAAAGAGTTTAATT | 10477 |
rs774986528 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053346 | TTTTGTGGACCAGGA[C/T]TTAAACCACCTTAGT | 10477 |
rs775036365 | in-del | -/CTC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983442 | AGGCCTATGTATTTT[-/CTC]CTCTTTCTCTCAATG | 10477 |
rs775056716 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180982392 | CATTCTTTAGGTGGT[A/G]TGTAAGCAACATTAC | 10477 |
rs775062374 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992822 | ATGTGCCACCACACT[A/C]AACTAATTTTGTATT | 10477 |
rs775106522 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014943 | GTGGAAGTGAAGTCA[A/C]TTTAGAATGGTGTGA | 10477 |
rs775112626 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180989578 | GTTATTTCCTCCATA[C/T]GTGCCAGTGTAGCAG | 10477 |
rs775178545 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020389 | CCATACTCTGGTATA[A/G]CCTCATCTTCACTAA | 10477 |
rs775182907 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050457 | GGACTCTTAGAGTAG[A/T]CACTTAAGCAGAGAT | 10477 |
rs775216971 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021248 | TGGAGTATTGTTTTC[C/T]CTTGTGAAGTCATAT | 10477 |
rs775218246 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034178 | AATCCCATTACTGGG[C/T]ATATACCCAAAGGAT | 10477 |
rs775225638 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028167 | TGTAATTACCTATTA[A/G]TGTAATTATTATAAT | 10477 |
rs775277005 | snp | A/G | 1.66299e-05 | 0.00288352 | splice-donor-variant | UBE2E3 | GRCh38.p7 | 2:181057826 | TTTAAGCCACCAAAG[A/G]TAAGAAGCTTGAAGT | 10477 |
rs775369719 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990627 | GTCTTCTGAGGCCAG[A/G]AATGCTTACAGCAGT | 10477 |
rs775399043 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996017 | TGGTGTCCTAGTATC[A/C]TTTTCAGAATGATTG | 10477 |
rs775417147 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988587 | AATGGGATTATATCA[A/G]CAGTTGTAAAATTCA | 10477 |
rs775454060 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026564 | TCCAAAGGCTGAGGA[A/G]ACAGAAAGTGAGAGA | 10477 |
rs775471162 | snp | G/T | 8.39624e-05 | 0.00647874 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060657 | GTTTTTAATGTGACT[G/T]TGCTTAGGTTACTTT | 10477 |
rs775498770 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997826 | TTCATCCTTCAAGTG[A/G]TAGTGATCTTTTAAA | 10477 |
rs775564240 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038677 | GGAGAAAATAATTTG[-/A]AAAACCTCTGTCTGA | 10477 |
rs775567994 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003151 | TATATGTGCCTTAAT[C/T]AGTATTCCCAGATAG | 10477 |
rs775579031 | snp | A/G | 3.40919e-05 | 0.00412853 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982262 | AAAGAAGGATCCAGC[A/G]CACTTTGTCAGGTTG | 10477 |
rs775675710 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985921 | CAGTTGCCAAAGAAA[C/T]CTACTTTACATGTTT | 10477 |
rs775743847 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994820 | TGGATACTAGTCTGT[A/T]TTATCATTTACTGCT | 10477 |
rs775762370 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042298 | ATCAGTTAATATTCT[C/G]TGCCTTCAGAGGCTG | 10477 |
rs775813148 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002507 | TGATTGCCATGATTT[A/G]CAACAGTGCTTTCCA | 10477 |
rs775813206 | snp | C/G | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991524 | AGCCAAGACCACTAC[C/G]AAGTGACTAGAGCAA | 10477 |
rs775824607 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047155 | ACACACTTTTCAAAC[A/C]CAGCTTCTTTCCATA | 10477 |
rs775914309 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053429 | TTTTGGAACATACTC[A/G]TTTATAAAAGTTAGT | 10477 |
rs775982774 | snp | A/G | 0.000101177 | 0.00711184 | missense | UBE2E3 | GRCh38.p7 | 2:181062809 | ATCCTCTGGTTGGAA[A/G]CATAGCCACTCAGTA | 10477 |
rs776119511 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059045 | TATATAGTACTGTAT[A/G]TGATTTGCCGTAATT | 10477 |
rs776122910 | in-del | -/ATC | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181053705 | CATTAACACATCATT[-/ATC]ATGCAAAGTCCCTAG | 10477 |
rs776137116 | snp | A/G | 0.000108123 | 0.00735187 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062763 | AGATACCACAAAATA[A/G]CTTTTAATGTTCTTT | 10477 |
rs776143923 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181011529 | AACCCATATAACAAG[C/T]CCAGTACTCTTCCCA | 10477 |
rs776158592 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026515 | TAGATCTTTCAACTA[-/T]TTTTTTTTTTTTTTA | 10477 |
rs776163297 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019318 | TTGATAGACGCTAAA[C/T]CATTGGAACATGTTC | 10477 |
rs776251998 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025984 | AAATATTTTAACGTC[A/G]TTCAAAACATACGTT | 10477 |
rs776352798 | snp | C/T | 1.65641e-05 | 0.00287781 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:181060691 | CACCAGAATCTATCA[C/T]TGCAACATCAACAGT | 10477 |
rs776384283 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180983974 | CATGGTGGTAGAGGG[C/T]AGTGTAATTCCCTGG | 10477 |
rs776386754 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997793 | CTTTGTTTACATCTC[C/T]CGTTGCCTAGGATGG | 10477 |
rs776417291 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037899 | CTTGAGCCCAGGAGT[C/T]CAAGATTGCAGTGAA | 10477 |
rs776437665 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986547 | TTAATTGACAAGTGC[A/G]TAAATGAGAATTTTA | 10477 |
rs776442994 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020275 | AGCTTGTGTTTTTGA[C/T]GTCACTCTACCTCCA | 10477 |
rs776468660 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001486 | CAAGAAGTGGAAATA[A/C]AACAAAAGAGACAAT | 10477 |
rs776475488 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996390 | AAGTTTTGAATTAAA[C/T]TGAGGGGGTAGTTTA | 10477 |
rs776500848 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040355 | CAATAAATTCAATTA[A/G]ATGTCATTTATTTCT | 10477 |
rs776589864 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045777 | TAGAATAACCTGGGA[A/G]ATTTTCTCCACACTG | 10477 |
rs776641536 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006765 | AAGCAACCCAACCTC[C/T]AAACATTTGTGTTTT | 10477 |
rs776814672 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054593 | GGTTGTTCATTTTCT[C/T]TAGTTTTAATGGTTC | 10477 |
rs776912179 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044715 | TTTTGTATGCTTATA[A/G]ATGGTAACATAATTC | 10477 |
rs776922258 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016395 | AATACCTTTTTGTCT[G/T]TATCAATAAAAATGA | 10477 |
rs776928818 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012137 | TCAGCAACTCCAGGT[A/T]TTTGTCACTTGTGAT | 10477 |
rs776953588 | in-del | -/TTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997250 | ATTTATCTATCTCTA[-/TTT]ATTTTTTTTCTGTCC | 10477 |
rs776997105 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051325 | ATTGGTAGACATAGT[A/G]GTTTTATGCAGTTTT | 10477 |
rs777005533 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003748 | TTACTTTTTCCTTAT[A/G]TGATGAATTGTTACA | 10477 |
rs777050118 | snp | C/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063546 | AAATAAACCCATTCT[C/T]AAATTGAAAACATTT | 10477 |
rs777063510 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181052856 | GTCTTCCATTTTCCT[A/G]TCTGCTGTGAAATGC | 10477 |
rs777073173 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181040306 | TCTCTAGTTCTGCAC[A/C]TGTTACACTGTATTG | 10477 |
rs777123963 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181013085 | TCCCACCTCAGCTTC[C/G]CGAGTAGCTGGGACT | 10477 |
rs777138765 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181044797 | ATTGCTCACTAGTTT[C/T]TGATTTAGCTTACTG | 10477 |
rs777180495 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994934 | TGGAGTCAAGAGAAT[C/T]GTTAATGTAAATATT | 10477 |
rs777190271 | in-del | -/CCC | 3.42959e-05 | 0.00414087 | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981998 | TTTTCTCCTCCTCCT[-/CCC]CCCCTGTTCTCTTTA | 10477 |
rs777224154 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985853 | TACGTGCATAAATCT[A/G]GAGAGCCTAGTAGAC | 10477 |
rs777405546 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012088 | GGAAACAAGTTAATT[A/G]ATGTTTTCTTTTGAG | 10477 |
rs777413963 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024263 | ATTGACACTTTATGT[C/G]AGAGTAAAACTTAAA | 10477 |
rs777443082 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060173 | ACCAACCGTCTTCTA[A/C]ATCCTCCAGTATTTT | 10477 |
rs777491525 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990139 | TTTTGATCAGTGGTT[C/T]TCAACTGAGGCAATT | 10477 |
rs777500611 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060421 | ATAGATGGAATTACT[A/G]TATCAGTTATTTAAG | 10477 |
rs777694042 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031607 | CTTAACGACTACTTT[C/G]TGTTTTTCTCTTTCT | 10477 |
rs777708848 | snp | A/G | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180992712 | TGTTACCCAGGCTAG[A/G]GTGAAATGGCGCAAT | 10477 |
rs777752153 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026316 | ATTTTTTTGTAATCT[-/G]ATTTTTTTTTTCAAT | 10477 |
rs777752775 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027950 | ACTGATGATTTCTCA[A/C]CCAGCTTAAAAACTA | 10477 |
rs777840824 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181038728 | CATGCAAGTCTTAAC[A/G]TACAAGTCTTATATC | 10477 |
rs777857349 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029269 | AGTATCTGTATTTTC[A/G]TTAGGAGCTGCCTGA | 10477 |
rs777867623 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057356 | TCAGGTGACTCAGAA[A/G]AAAGTATGTCTCTAT | 10477 |
rs777870508 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181042593 | GTGCCAAACTGGAAG[C/T]CATGGAACAGGTTAG | 10477 |
rs777950060 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181016161 | CTGAATTTTAACCCT[A/G]AATCTGCCACTGATT | 10477 |
rs777990754 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034706 | AGAAATTTCCTGGAA[C/G]TAGCATGTCAGAATA | 10477 |
rs778000019 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998614 | TCATGCAAAATCACC[A/G]TTGGTAATAATGTGG | 10477 |
rs778113675 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181058701 | TGTTGCAGTCTATAC[A/C]ATTTAAAATTTATGT | 10477 |
rs778135441 | in-del | -/AGA | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181025045 | CACTATAAGCCTTTC[-/AGA]ATGTGGCTTTAGTTA | 10477 |
rs778249431 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005998 | CTAAGCCAAGAGCTG[C/G]TGATGTAAACACCAG | 10477 |
rs778268767 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181024233 | AGCCTCTTGACTGAC[C/T]CTTCTCAGAAAATGA | 10477 |
rs778285822 | snp | C/T | 1.66065e-05 | 0.00288149 | missense, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982188 | AGCAGAAGAAAAACA[C/T]CAAACTCTCTAGCAA | 10477 |
rs778339282 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181005114 | AAAACATAAATTTGT[G/T]GGCTCACATAACTGA | 10477 |
rs778429257 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017901 | GATTTTTTGGTTAGA[A/G]GAATCCCAGCTTCAT | 10477 |
rs778452759 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180993768 | GGTCCCGAAGAGAAT[C/G]GATCTCAGAAGATTG | 10477 |
rs778570057 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180994487 | TGCACTTTCAAAAGA[A/T]AAGACTCCTTTTAAC | 10477 |
rs778583253 | in-del | -/TTG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181028708 | TGAAATGCCTTTTTT[-/TTG]TTATTTGTCCCCCTG | 10477 |
rs778650372 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007523 | TTTTTTTCTTTCTTT[A/G]TACTTGGAAATACCT | 10477 |
rs778702129 | snp | A/T | 1.69135e-05 | 0.002908 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060648 | TTTCCTTCTGTTTTT[A/T]ATGTGACTGTGCTTA | 10477 |
rs778724981 | in-del | -/C | | | | | GRCh38.p7 | 2:181021578 | CCTTCCTTCCTCCCT[-/C]CCTCCCTTCCTTCCT | 10477 |
rs778744629 | snp | C/T | 4.97162e-05 | 0.00498554 | | | GRCh38.p7 | 2:180982162 | AGAGGAAAGAAAACC[C/T]TCTGCCACCCAGCAG | 10477 |
rs778764162 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180990939 | TCAGAATGCAGAAAG[C/T]TTCATGTTTTAGAAA | 10477 |
rs778784353 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017244 | TTACATTAAAGTGGG[-/T]ATACAGTGGTCAAGA | 10477 |
rs778848213 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002079 | TAGTTGGCATTAGCT[A/G]GAAATACATATGGCC | 10477 |
rs778854110 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012909 | TAGACATTGCTTGGT[A/G]TTTAGAATATACCAG | 10477 |
rs778871349 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986377 | CTTCAAATTCTTGTG[A/G]GTGGAAGAAGACCTA | 10477 |
rs778879163 | in-del | -/AG | 5.01584e-05 | 0.00500766 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057850 | TGAAGTGCATTCTTT[-/AG]AGTATTTAATCCTTC | 10477 |
rs778886884 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181054086 | CACAGTTTATATATC[C/T]ATTCACCTACTGAAG | 10477 |
rs778932568 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998534 | AATTAAGATCATGTT[C/T]CCTACTTGATTTTAG | 10477 |
rs778978023 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049653 | ACTATATGGTAATTA[C/T]TAGATCAAGAAAGCA | 10477 |
rs779004781 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020853 | CCTGACATGGGTAAA[G/T]CTAGTGATATGGTTG | 10477 |
rs779019496 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014400 | TAGATGGCAGTATGT[A/C]TCAATAAAGTTCACT | 10477 |
rs779020470 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181008606 | AGGGCAGCATTAGGG[G/T]CAGCCCCAGGTTCTA | 10477 |
rs779060058 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181012700 | TACATATACCCATAT[C/T]CCTAGTTGTTAGTTA | 10477 |
rs779089142 | snp | G/T | 1.68895e-05 | 0.00290593 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060835 | AATCTTTATTAACAT[G/T]TACAATAAGACTACA | 10477 |
rs779091583 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026632 | TTAGTTAAAGTTTCA[C/T]TAATGCCATTAATTT | 10477 |
rs779110610 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007386 | ACATGTTGCTCCCTA[C/T]TGATAATCAGACCTT | 10477 |
rs779111600 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050442 | CCTAAAGTTTGGGAG[A/G]GACTCTTAGAGTAGA | 10477 |
rs779245437 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035603 | CTTGTTCAACCCATG[A/T]CCCGTGGGTCACATG | 10477 |
rs779330701 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981467 | GGCCGTGGAAACAGC[C/T]AGAGCAGCTCGTTAG | 10477 |
rs779360602 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056835 | TAAGCAGTAGGAAAA[C/T]TGGATAGCAGTTTGT | 10477 |
rs779383174 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181062689 | GCTATTATATATGAA[G/T]ATACTGCTGAAAAAT | 10477 |
rs779383428 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181034829 | ACAAATGTGGCTTTC[A/G]ACAGGTGAAATGATT | 10477 |
rs779396256 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017668 | TTTTTTTTTTAATAC[A/G]GAAGTGTCATATGTT | 10477 |
rs779485724 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002329 | TTTTCTGTTGCTCAC[C/T]GCGTTAGGTAAGGCA | 10477 |
rs779494297 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060891 | TTTTTTTTTTTTTAG[-/T]TAGCTTTAAATGTAG | 10477 |
rs779570684 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027625 | CCTTAATAAAACAGT[A/G]TGTAATTGTGAGAAG | 10477 |
rs779591741 | in-del | -/TATTGATG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029782 | ACTTGTCATCTTTAA[-/TATTGATG]TATTGATGTTTGGCG | 10477 |
rs779593218 | snp | C/T | 1.70179e-05 | 0.00291696 | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984027 | TCCTTTTTGTCTCTT[C/T]TCATTTCACTAACAG | 10477 |
rs779598428 | snp | C/G | 1.65745e-05 | 0.00287871 | synonymous-codon, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180982171 | AAAACCTTCTGCCAC[C/G]CAGCAGAAGAAAAAC | 10477 |
rs779625637 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181004054 | CAGGTGTGAATGTGT[A/G]TGTGGGAAGGTCTTG | 10477 |
rs779739639 | in-del | -/TTTTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs779758661 | in-del | -/TG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018362 | ATATTTTTATCTCTG[-/TG]TGTGTGTGTATATAT | 10477 |
rs779826029 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050903 | GAAACTTCCTTCTTT[C/T]TTGTTTCAACGTACA | 10477 |
rs779903803 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984271 | GGAGAAAAAATACTT[C/T]TTAGCATAAGTATAC | 10477 |
rs779956462 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181051957 | TCCAAATAAAATTTT[G/T]TATAGAGTCTGAAGA | 10477 |
rs780001265 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180985371 | GGGTAAAATTTATAC[A/G]CATTGGATTTTAAAA | 10477 |
rs780048992 | in-del | -/TTTG | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180991647 | GATTTTTTTTGCGAT[-/TTTG]TTTGTTTGTTTTTTT | 10477 |
rs780058853 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006493 | TAAAATTGAATTTCA[A/G]ATAAACAATAATTTT | 10477 |
rs780075279 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180979281 | GCACCTAGCAACATA[C/T]AGCCCTCAATAAAGT | 10477 |
rs780084845 | snp | A/G | 3.64451e-05 | 0.00426863 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062901 | TAATTCACATAATTT[A/G]TATGCAGTGTGAAGG | 10477 |
rs780098913 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014780 | ATATGATACCTTTAT[A/G]TGATGTATAATGATC | 10477 |
rs780106800 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059562 | TTGTCATTTCAACAT[A/G]TAATCCGTGTAAGAG | 10477 |
rs780146251 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022718 | CATGGTACTAAGTAG[A/G]CTGCAAAAAAAAACA | 10477 |
rs780154165 | snp | A/G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180996970 | GAGCTTAATGTGTAC[A/G/T]TATGCACACATGGCT | 10477 |
rs780169414 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019607 | TATTTTCATTGGGGA[A/G]CACAATGTACCAGTG | 10477 |
rs780171635 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180980203 | GTACTGGGGCCCCGG[A/G]AGCCACGACGGCCCC | 10477 |
rs780178091 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180998536 | TTAAGATCATGTTTC[C/G]TACTTGATTTTAGTT | 10477 |
rs780215415 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181049404 | GATGTGTGTTTGTGT[A/G]TGTTTTTTAAATTAT | 10477 |
rs780262342 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181031419 | CTTGAGGCTATTTTA[C/T]TATGTAGAGCAAGCT | 10477 |
rs780263392 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181014477 | GAGAAGAGTTAACTT[A/T]TAATGATTGATTAGG | 10477 |
rs780298133 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997321 | TGGCTTTTCCTCTTT[-/C]ATTTTATTTTAGAAA | 10477 |
rs780309661 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030341 | TTTTTTGAGACGGAG[-/T]CTTGCTCTGTCGCCC | 10477 |
rs780338493 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048277 | CTTGGCTGAAATCTC[C/T]ATTGTATATTTAGTT | 10477 |
rs780349388 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026427 | TTTTGATTCCTGCTG[A/G]TTTCTCTATCTTGTT | 10477 |
rs780358264 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181056640 | CCCAGACACTTCCCA[A/G]CATTGCCGCGTTTGG | 10477 |
rs780445658 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181027354 | CTTGGTAGCTGCATC[A/G]TATATCATGGTCATC | 10477 |
rs780508645 | in-del | -/TTTTTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060862 | TACAAAAACGAGTGC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 10477 |
rs780552879 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988961 | AATCTTAATTGGAAG[C/T]TCGACTGTAAAACAG | 10477 |
rs780611110 | in-del | -/TTCTC | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180992170 | TGCTTAAGAGTTCTT[-/TTCTC]TTAAGGTGAAACTAT | 10477 |
rs780629858 | snp | A/G | 1.66674e-05 | 0.00288676 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057670 | ATATATGTACATACT[A/G]ATTTTTAATTTCTTT | 10477 |
rs780633477 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180984020 | TATCAAATCCTTTTT[A/G]TCTCTTCTCATTTCA | 10477 |
rs780639197 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181017957 | TTCTGAGCGTGACTC[-/T]TCTTTTTTCTGTATT | 10477 |
rs780710654 | snp | A/C | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180988259 | CATTTTCTCTAGTGC[A/C]TTGACATCTTATGTA | 10477 |
rs780720755 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037478 | CCTGAGCCTGTGTGA[C/G]CCTAGGCTAATGTGT | 10477 |
rs780784071 | snp | A/C | | | intron-variant, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181043933 | TTCGTTGGACATTTA[A/C]GTTATTTTGAGTTTC | 10477 |
rs780809646 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181002422 | AGATACCTATCAATT[C/G]ACAATACTTTTTTTG | 10477 |
rs780825584 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181022501 | ACATCTTCTCAGTGT[A/G]TATTGTTGATTCATT | 10477 |
rs780913977 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181003731 | GACATTTTTATTGCC[A/G]TTTACTTTTTCCTTA | 10477 |
rs780928807 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050665 | ATTTGTGGTGAAGAC[A/G]TTTTAGAAGAGAATC | 10477 |
rs780948948 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181043416 | ATGCACAAAATTATT[C/T]AAAATATTGTATAAA | 10477 |
rs781026081 | snp | A/C/G | 0.00010029 | 0.00708067 | synonymous-codon | UBE2E3 | GRCh38.p7 | 2:180984070 | GCTAGCTGAAATAAC[A/C/G]CTTGATCCTCCTCCT | 10477 |
rs781055359 | snp | C/T | | | downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:181063644 | GTGGATTTTGACCCA[C/T]TGGTCTCAAACACAT | 10477 |
rs781073922 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060650 | TCCTTCTGTTTTTAA[C/T]GTGACTGTGCTTAGG | 10477 |
rs781085345 | snp | A/G | 5.79727e-05 | 0.00538359 | utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:181062924 | TGTGAAGGAGCAGAA[A/G]GCATCTTCTCACTGT | 10477 |
rs781089082 | in-del | AGTTAGCTTTAAATG/TTTTTTTTAAATGTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181060889 | TTTTTTTTTTTTTTT[lengthTooLong]TAGATTGAGAGGTAA | 10477 |
rs781193655 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018040 | CCTAATTTTGTTTTC[A/G]TTGTATTTTTAACCT | 10477 |
rs781211780 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981983 | TTTCCTAGATTTAAC[A/T]TTTTCTCCTCCTCCT | 10477 |
rs781266817 | in-del | -/TT | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978686 | AGTAATTGAAATAAC[-/TT]AACTTGCCTGAGGTC | 10477 |
rs781277546 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180978798 | ACCAAACAACTAAAT[A/G]TCTTTCTCCCCTAAG | 10477 |
rs781291410 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995740 | CAAATTCAGGCTGGA[-/T]TTTTTTTTTTTTTTC | 10477 |
rs781311985 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019116 | CTACAGGCATGTGCC[A/G]CCACACCTGGCTGAT | 10477 |
rs781314600 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030609 | TTTATTTTTTATTTT[C/T]GATTCTCAGAAGCGT | 10477 |
rs781326270 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE2E3, LOC105373772 | GRCh38.p7 | 2:180981778 | CAATTGATAGATTGT[C/T]CAAGAGACGGAAAAA | 10477 |
rs781380938 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181059251 | TTATTTCTCTGCAAT[A/G]CTAAATCTTTTTGAA | 10477 |
rs781449630 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181036681 | GCTGCTGGAACTCTT[C/T]AGCCACCCTCTACCC | 10477 |
rs781495738 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | UBE2E3 | GRCh38.p7 | 2:180990379 | GACCCTCCTATAGAT[A/C]TTTGTTCCTGTACTT | 10477 |
rs781496755 | snp | A/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181007181 | GGATTACAATTTGGA[A/T]AAATCAGATCTTAAT | 10477 |
rs781608564 | snp | C/T | 5.04936e-05 | 0.00502436 | intron-variant | UBE2E3 | GRCh38.p7 | 2:181057867 | GTATTTAATCCTTCT[C/T]CTCTAAAATCGGTTA | 10477 |
rs781635215 | in-del | -/GT | | | intron-variant, frameshift-variant | UBE2E3 | GRCh38.p7 | 2:180987472 | ACGAATATTTTAAGA[-/GT]GTATGTTCAGATTGA | 10477 |
rs781662467 | in-del | -/TTTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018600 | TTTCAATTTCTGTGT[-/TTTTT]TTTTTTTTTTTTCCA | 10477 |
rs781675227 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029565 | GTTTTATCTAAAAAC[-/T]TTGTTTTTTATCTAG | 10477 |
rs781685204 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180986856 | AAGAAAACTCAGCAA[A/C]ACCAAAATTATTCAG | 10477 |
rs781709126 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006525 | ATAAGTATGTCCCAA[A/G]TGTACATGGAGCACA | 10477 |
rs781713402 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181035953 | GTATAAAGTAAGCCT[C/G]CAATGTGGTAAGTGA | 10477 |
rs781739521 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180995617 | AAGAAACTGGGCTGA[A/G]TTTCCTTAGAGTCTG | 10477 |
rs781745270 | snp | A/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181037479 | CTGAGCCTGTGTGAG[A/C]CTAGGCTAATGTGTA | 10477 |
rs781759546 | snp | G/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181048154 | CTCTGACTCTTCCCT[G/T]ATCTCTCTAACATTT | 10477 |
rs796071140 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181026203 | TAAATTTTGAAAATA[A/G]TGATTGAAGCTAATA | 10477 |
rs796072261 | in-del | -/C | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030743 | ATTAACTACAAGTCC[-/C]ATCTCTATATTGTAT | 10477 |
rs796091273 | multinucleotide-polymorphism | CCCTC/TCTTT | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021666 | CTTCCTTCCTTCCTT[CCCTC/TCTTT]CTTCCTTCCCAACTT | 10477 |
rs796127463 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181030365 | GTCGCCCAGGCTGGA[C/G]TGCAGTGGCACGATC | 10477 |
rs796159780 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021654 | CCTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCTT | 10477 |
rs796166551 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181006389 | GTGATTTCAGATTTT[-/T]GTTGCCTTCCACCTT | 10477 |
rs796170250 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181045879 | GATATGTTGGGACAG[-/A]AAAAAAAAAAGACAA | 10477 |
rs796276759 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021385 | TTTCTTTTCTTTTTT[-/T]CCTCTTTTCTCTTTT | 10477 |
rs796295637 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181041254 | AAAAAAAAAAAAAAA[A/G]ATAGATTTTTTTTTT | 10477 |
rs796354029 | in-del | CCCTC/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021645 | TTTCCTTCCTTCCTT[CCCTC/T]CTTCCTTCCTTCCTT | 10477 |
rs796361112 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181029135 | CATGATTCTTTTTTT[A/G]CCTAGTTCTGTGTTG | 10477 |
rs796378535 | snp | A/G | | | intron-variant, missense | UBE2E3 | GRCh38.p7 | 2:181043878 | TTTTTCAGTGCCTAC[A/G]TCATGATTGATTGAA | 10477 |
rs796394333 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181050775 | TACTCGAACAGGATT[A/G]CTACTATTGAGTTAG | 10477 |
rs796426060 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021642 | CCTTTTTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 10477 |
rs796429085 | in-del | -/TGAG | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181020314 | TGGCTGCCTTCTTCC[-/TGAG]TATCTCTGTCTCTCT | 10477 |
rs796446412 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019837 | CTTTTAATTTTTTTC[-/T]TTTTTTTTGTGGTGA | 10477 |
rs796465868 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBE2E3 | GRCh38.p7 | 2:180987642 | ATTTCGTTGACTTTC[C/T]TCTTTAAAAATAAAA | 10477 |
rs796495893 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021610 | CCTCCCTTCCTTCCT[C/T]CCTCCCTCTCTCCCT | 10477 |
rs796497344 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021582 | CCTTCCTCCCTCCCT[C/T]CCTTCCTTCCTCCCT | 10477 |
rs796515484 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181001219 | TAGTGTTTTAGAAAC[A/G]TGAGTTACTACATTT | 10477 |
rs796669339 | snp | C/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181047273 | ATTATTGGGACTTAG[C/G]TGTGGTGGTCTCATC | 10477 |
rs796715233 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:180997122 | ACACTTTTTTTTTTT[-/A]ACCCTTCTAATCTCT | 10477 |
rs796742541 | in-del | -/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181055982 | TAGGACTCAGATCTT[-/G]GTTTTTCTTACAACA | 10477 |
rs796825667 | in-del | -/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181061789 | CCTTTTTTTTTTTTT[-/T]AAGTTGACTTACTTC | 10477 |
rs796856771 | in-del | -/A | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018189 | GAATGTATAATAAAA[-/A]CAGTTATACTCTAGT | 10477 |
rs796857106 | snp | A/G | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181019373 | CATAAATGTCACTCA[A/G]AAGCATATTAACCTT | 10477 |
rs796894011 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181021674 | CCTTCCTTCTTTCCT[C/T]CCTTCCCAACTTTTC | 10477 |
rs796926911 | snp | C/T | | | intron-variant | UBE2E3 | GRCh38.p7 | 2:181018129 | GACTTTCATTTTCTT[C/T]ACTCTTCTTGGTACT | 10477 |