SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7807 | snp | G/T | 0.40733 | 0.194287 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268948 | GTGACAGTAAAATAC[G/T]AGACATAGAAGAGAT | 9690 |
rs8101 | snp | A/G | 0.498059 | 0.0310896 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268780 | GCAAGAACTACCGAC[A/G]CTCCTCTTCCCTGGA | 9690 |
rs733483 | snp | C/T | 0.298398 | 0.245271 | intron-variant | UBE3C | GRCh38.p7 | 7:157159439 | TTTTACTTGGTAATA[C/T]TCACATATTAATAAA | 9690 |
rs869300 | snp | A/G | 0.329317 | 0.237084 | intron-variant | UBE3C | GRCh38.p7 | 7:157178158 | CCGACTGCTTGTGCT[A/G]CCCTCTCTAAACGGA | 9690 |
rs870745 | snp | A/G | 0.49635 | 0.0425631 | intron-variant | UBE3C | GRCh38.p7 | 7:157178887 | TGCTCACTCCCCATC[A/G]GGATGCTGAGCCACA | 9690 |
rs886677 | snp | A/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157211088 | CCCTATCACAGGAGG[A/T]AACTCCTGTTAAGTT | 9690 |
rs886678 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157210739 | TGTCAAAATCAATGG[A/G]AGGCAGGAGATCATG | 9690 |
rs886679 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | UBE3C | GRCh38.p7 | 7:157210714 | ATCATGGGCTAAACG[C/T]TTCTGCGTTCTTTGG | 9690 |
rs929354 | snp | A/G | 0.497803 | 0.033074 | intron-variant | UBE3C | GRCh38.p7 | 7:157252863 | CTGGGGTTAGATGAG[A/G]GCAACCTATACTGTG | 9690 |
rs933344 | snp | A/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157218571 | GTGGGCAGAGTTAGA[A/T]GCAACAGGCTTAACT | 9690 |
rs1002388 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157173384 | TCAGTTCTCAAGCAT[A/G]GATGCGATAGCAATA | 9690 |
rs1002389 | snp | C/G | 0.499598 | 0.0141716 | intron-variant | UBE3C | GRCh38.p7 | 7:157175629 | TGTCCAGAAAATTAA[C/G]TGAAATTATATGGAA | 9690 |
rs1003373 | snp | C/G | 0.216649 | 0.247765 | intron-variant | UBE3C | GRCh38.p7 | 7:157239552 | GTGCCCTAATCACAA[C/G]CCTGTGGTTCCATCC | 9690 |
rs1014248 | snp | C/G | 0.257732 | 0.24988 | intron-variant | UBE3C | GRCh38.p7 | 7:157204366 | ttgcgccattgcact[C/G]cagcctgggtaacaa | 9690 |
rs1034785 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157209689 | TGAAACTCTCAACAG[A/G]TGCCATAAAACAGTG | 9690 |
rs1057014 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268521 | CAACATCTGTCACCC[A/C]CTATACCCAGTTACT | 9690 |
rs1151788 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157243848 | tcagggaccacatta[C/T]atactggAATTCTGC | 9690 |
rs1176632 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245967 | ctccctctgttgccc[A/G]ggctggagtgcagcc | 9690 |
rs1176633 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245939 | cagtggcacgatctc[A/G]gctcactgcaacctc | 9690 |
rs1176634 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245928 | tctcggctcactgca[A/G]cctccgcctcccagg | 9690 |
rs1176635 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157245852 | aggtgtgcaccacca[G/T]gcccagctaattttt | 9690 |
rs1176636 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | UBE3C | GRCh38.p7 | 7:157237090 | TTTAACTGTAGAATC[G/T]AAACCACTTGTATTT | 9690 |
rs1176637 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157234433 | GACCATATTGCATAA[A/G]GGCagacccagagtg | 9690 |
rs1176638 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | UBE3C | GRCh38.p7 | 7:157229782 | tctacaaaatataag[A/T]aaagctgggcatggt | 9690 |
rs1182360 | snp | C/G | 0.499382 | 0.017561 | intron-variant | UBE3C | GRCh38.p7 | 7:157227856 | CAAATCTTTTAACTT[C/G]AATGCAATTATTAGC | 9690 |
rs1182361 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157227464 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 9690 |
rs1182362 | snp | C/T | 0.499885 | 0.00758699 | intron-variant | UBE3C | GRCh38.p7 | 7:157226841 | ACAAACCTGGCCCTG[C/T]GGAGAGGCCACAGCC | 9690 |
rs1182363 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | UBE3C | GRCh38.p7 | 7:157226457 | TTAATCCCCTCGGCA[C/T]TGACCAACATGGAAT | 9690 |
rs1182364 | snp | A/G | 0.499897 | 0.00718776 | intron-variant | UBE3C | GRCh38.p7 | 7:157225218 | GTATATCATATTTAA[A/G]TATTTCTAAAGCTGC | 9690 |
rs1182365 | snp | A/T | 0.499368 | 0.0177603 | intron-variant | UBE3C | GRCh38.p7 | 7:157224561 | ATATAAACAAAGTTT[A/T]GTACATCAAAGACAC | 9690 |
rs1182370 | snp | G/T | 0.406468 | 0.194981 | intron-variant | UBE3C | GRCh38.p7 | 7:157258718 | aatcccagcactttg[G/T]gaggctgaggtaggt | 9690 |
rs1182371 | snp | A/G | 0.406468 | 0.194981 | intron-variant | UBE3C | GRCh38.p7 | 7:157258706 | ttgggaggctgaggt[A/G]ggtggatcacctgag | 9690 |
rs1182372 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UBE3C | GRCh38.p7 | 7:157258526 | gttgcagtgagcgga[A/G]atcacgccattgccc | 9690 |
rs1182373 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | UBE3C | GRCh38.p7 | 7:157256836 | gggattggtccagac[A/C]cccacggaaactaaa | 9690 |
rs1182374 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | UBE3C | GRCh38.p7 | 7:157256246 | ctgaggtgggagaat[C/T]gcttgaacccagaag | 9690 |
rs1182375 | snp | C/G | 0.497722 | 0.0336691 | intron-variant | UBE3C | GRCh38.p7 | 7:157256224 | acccagaaggcagag[C/G]ctgcagtgagctgag | 9690 |
rs1182376 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UBE3C | GRCh38.p7 | 7:157256094 | TATAAAGATGAATGC[A/G]GGCACCAAGAACTAC | 9690 |
rs1182377 | snp | C/T | 0.4862 | 0.0819127 | intron-variant | UBE3C | GRCh38.p7 | 7:157255709 | ACTTAAGACATTTTA[C/T]TGGTGTTATTTCTGT | 9690 |
rs1182378 | snp | C/T | 0.497933 | 0.032082 | intron-variant | UBE3C | GRCh38.p7 | 7:157255628 | GAGGGCTTGCACCTT[C/T]AATAATCTCAGCTAT | 9690 |
rs1182379 | snp | A/C/T | 0.0549835 | 0.157627 | intron-variant | UBE3C | GRCh38.p7 | 7:157253436 | AACGATCAGTGATAA[A/C/T]AGATCAGCCAATTTC | 9690 |
rs1182380 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE3C | GRCh38.p7 | 7:157252571 | GGTTCTCATTTTATA[C/T]AGAATGTTCAAATTG | 9690 |
rs1182381 | snp | C/T | 0.497855 | 0.0326773 | intron-variant | UBE3C | GRCh38.p7 | 7:157250779 | AGACCTAGCAGCAAG[C/T]GACATCACTGGATGT | 9690 |
rs1182382 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | UBE3C | GRCh38.p7 | 7:157250244 | tgggtgacagagtga[A/G]accccgtctcaaaaC | 9690 |
rs1182383 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | UBE3C | GRCh38.p7 | 7:157249859 | tcagattatggatgc[A/T]caGAGTGTATTTGAA | 9690 |
rs1182384 | snp | C/T | 0.497933 | 0.032082 | intron-variant | UBE3C | GRCh38.p7 | 7:157247948 | CACGCCTCGCAGCTA[C/T]TGGACCCTATTTCCA | 9690 |
rs1182385 | snp | A/G | 0.497829 | 0.0328757 | intron-variant | UBE3C | GRCh38.p7 | 7:157247889 | tttccaaacaaggcc[A/G]tgcccacaggatggg | 9690 |
rs1182386 | snp | C/T | 0.497855 | 0.0326773 | intron-variant | UBE3C | GRCh38.p7 | 7:157247649 | gctggagtgcagccg[C/T]gcgatctcagctcac | 9690 |
rs1182387 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE3C | GRCh38.p7 | 7:157246892 | caaaaaaagagaaaa[C/T]ATCCAGTCTTCAGAG | 9690 |
rs1182388 | snp | A/G | 0.255782 | 0.249933 | intron-variant | UBE3C | GRCh38.p7 | 7:157246788 | AACAGGTGGAGAACA[A/G]TTTTAGAGAAAGAAA | 9690 |
rs1182389 | snp | C/T | 0.497907 | 0.0322805 | intron-variant | UBE3C | GRCh38.p7 | 7:157246109 | TACGACTGGAGAAAA[C/T]GAGAAAATAGCTGTT | 9690 |
rs1182390 | snp | C/T | 0.46885 | 0.12085 | intron-variant | UBE3C | GRCh38.p7 | 7:157245864 | AGCTGGGACTACAGG[C/T]GTGCACCACCAGGCC | 9690 |
rs1182391 | snp | A/G | 0.473818 | 0.111381 | intron-variant | UBE3C | GRCh38.p7 | 7:157245674 | TCTGCCAGGTAAACC[A/G]AAGTATTATGTCCTT | 9690 |
rs1182392 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | UBE3C | GRCh38.p7 | 7:157243506 | AGCCAATCTCTAAAC[A/G]TGAGCTGAGGTGAAC | 9690 |
rs1182393 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | UBE3C | GRCh38.p7 | 7:157243244 | CAAGGAAAGCCTGCA[C/G]AGATTGCCCTTCTCA | 9690 |
rs1182394 | snp | C/T | 0.499908 | 0.00678851 | intron-variant | UBE3C | GRCh38.p7 | 7:157242980 | ATAATCTCTGCCTTC[C/T]GGTTTCAAGCGATTT | 9690 |
rs1182395 | snp | A/C | 0.499396 | 0.0173617 | intron-variant | UBE3C | GRCh38.p7 | 7:157240230 | ccatctctacaaaaa[A/C]cacaaaaattagccg | 9690 |
rs1182396 | snp | G/T | 0.499396 | 0.0173617 | intron-variant | UBE3C | GRCh38.p7 | 7:157239137 | cacatgtattctaat[G/T]aataggtacacattt | 9690 |
rs1182397 | snp | A/C | 0.190205 | 0.242744 | intron-variant | UBE3C | GRCh38.p7 | 7:157238713 | gatctaattcaggct[A/C]atgaccttaaggacc | 9690 |
rs1182398 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157238575 | tcctgcccgcacctt[C/T]cccagcttagtcagc | 9690 |
rs1182399 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157238282 | TTCTGCTGCCCTCTG[C/T]TGGTGACGCCAGGAG | 9690 |
rs1182412 | snp | C/T | 0.305436 | 0.243776 | intron-variant | UBE3C | GRCh38.p7 | 7:157267283 | aggtgcctgccacca[C/T]gcctggctaattttt | 9690 |
rs1182413 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | UBE3C | GRCh38.p7 | 7:157265863 | CAGATGTGTTCATGA[C/T]GTTCTGGTATTTAAA | 9690 |
rs1182414 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | UBE3C | GRCh38.p7 | 7:157265669 | CACAGTATTCCGTGC[C/T]GTGCTTTTCTCATCT | 9690 |
rs1182432 | snp | A/G | 0.499382 | 0.017561 | intron-variant | UBE3C | GRCh38.p7 | 7:157236482 | ACACTGAATTCTACC[A/G]CGATAAAAAATTATA | 9690 |
rs1182433 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | UBE3C | GRCh38.p7 | 7:157236181 | CTGTCTGCAGCCTGA[C/T]TTACAGGCGACAAAA | 9690 |
rs1182434 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157236170 | CTGACTTACAGGCGA[C/T]AAAATGCAATCATGA | 9690 |
rs1182435 | snp | C/G | 0.499354 | 0.0179596 | intron-variant | UBE3C | GRCh38.p7 | 7:157235105 | CCTCCAGGTTCAAGC[C/G]ATTATCCTGCCTCAG | 9690 |
rs1182436 | snp | A/G | 0.391769 | 0.205917 | intron-variant | UBE3C | GRCh38.p7 | 7:157235059 | GGATTAAAGGCATGC[A/G]CCACCACGCCCAGCT | 9690 |
rs1182437 | snp | A/G | 0.49934 | 0.0181589 | intron-variant | UBE3C | GRCh38.p7 | 7:157234974 | GAGCTCCCGACCTCA[A/G]GTGATCCGCCTGCCT | 9690 |
rs1182438 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | UBE3C | GRCh38.p7 | 7:157234744 | ACACCTGAAATCTGC[C/T]ACCTGAAATACGGTG | 9690 |
rs1182439 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | UBE3C | GRCh38.p7 | 7:157234673 | GAAGTCAGGTTGGAG[C/T]CCTTTCTCAAACCTG | 9690 |
rs1182440 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157234441 | GTAATCAAGACCATA[C/T]TGCATAAGGGCagac | 9690 |
rs1182441 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | UBE3C | GRCh38.p7 | 7:157233956 | aagcacatgaaaaga[C/T]ggtcaacattattag | 9690 |
rs1182442 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | UBE3C | GRCh38.p7 | 7:157233939 | gtcaacattattagt[C/T]accagggaaattaaa | 9690 |
rs1182443 | snp | C/T | 0.408359 | 0.193449 | intron-variant | UBE3C | GRCh38.p7 | 7:157233358 | cgcaggactgagccg[C/T]gtttgtagcagtgca | 9690 |
rs1182444 | snp | C/T | 0.49941 | 0.0171624 | intron-variant | UBE3C | GRCh38.p7 | 7:157231816 | ttataacagaagacc[C/T]gaaactgagtaatta | 9690 |
rs1182445 | snp | C/G | 0.499368 | 0.0177603 | intron-variant | UBE3C | GRCh38.p7 | 7:157231734 | cagaggcagcccctg[C/G]tgaggtcttctcatt | 9690 |
rs1182447 | snp | C/T | 0.190519 | 0.242821 | intron-variant | UBE3C | GRCh38.p7 | 7:157229311 | acaaacaaacaaaaa[C/T]ccaaaaccaaaaaaA | 9690 |
rs1182448 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | UBE3C | GRCh38.p7 | 7:157228721 | ATGGACAAGATGGGG[C/T]CACTCTGCACAGCAG | 9690 |
rs1182449 | snp | C/T | 0.486529 | 0.0809556 | intron-variant | UBE3C | GRCh38.p7 | 7:157262635 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 9690 |
rs1182450 | snp | C/T | 0.432944 | 0.170387 | intron-variant | UBE3C | GRCh38.p7 | 7:157261385 | TCAATTATGATTGTG[C/T]GGGGTCTTGACTGGG | 9690 |
rs1182451 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157261307 | TTTTTTTTTTTTTTT[C/T]CAGACAGAGTTTTGC | 9690 |
rs1182452 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | UBE3C | GRCh38.p7 | 7:157260924 | GGCCATGCACGAACC[C/T]GGAGGCATCACGGAG | 9690 |
rs1183107 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | UBE3C | GRCh38.p7 | 7:157237001 | ctcacgcctgtaatg[C/T]cagcactttggaagg | 9690 |
rs1184670 | snp | C/T | 0.433236 | 0.170072 | intron-variant | UBE3C | GRCh38.p7 | 7:157264092 | CTCACACCTGTAATA[C/T]CAGGTGTGTGTGTGT | 9690 |
rs1306261 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247572 | ccccagtagctggga[C/T]tacaggcatccacca | 9690 |
rs1306262 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247533 | agctaatttttgtat[A/T]tttagtagagatgga | 9690 |
rs1307002 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247596 | caagcgattctcctg[C/T]ctcagtttccccagt | 9690 |
rs1544449 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157201550 | CCAGCCATTTGATGA[G/T]ACACCGAGACACGGC | 9690 |
rs1636067 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230467 | ccttgtgatctgccc[A/G]ccttggcttcccaaa | 9690 |
rs1636602 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157237022 | CTGTCTTGCCGGGTG[C/T]GCTGGCTCACGCCTG | 9690 |
rs1636603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157236747 | gagactccatctcaa[A/G]aaaagagaaaaaaaa | 9690 |
rs1636606 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230556 | aggcgtgtgccacca[C/T]acctggctaattttt | 9690 |
rs1636607 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230555 | ggcgtgtgccaccac[A/G]cctggctaatttttc | 9690 |
rs1636608 | snp | G/T | 0.382473 | 0.212016 | intron-variant | UBE3C | GRCh38.p7 | 7:157227946 | ACATGGCTTAATCAT[G/T]CTTACAGTATTTGAG | 9690 |
rs1808217 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157210047 | TGGGATTACAGGCGT[A/G]CATCACGCCCAGCTA | 9690 |
rs1833097 | snp | C/G | 0.187369 | 0.242028 | intron-variant | UBE3C | GRCh38.p7 | 7:157242828 | acctcgtgattctcc[C/G]gccttggcctcccaa | 9690 |
rs1833098 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | UBE3C | GRCh38.p7 | 7:157242771 | CCAGACCTGGCTCGA[C/T]CCTTCCTTTTTTTCC | 9690 |
rs1859550 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | UBE3C | GRCh38.p7 | 7:157195701 | CACTAAAGCCATCTA[A/C]ATTTGGGAGAGGATC | 9690 |
rs2006844 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157210157 | GAGAGAGTCACCCTA[C/T]CGCCCAGGCTGGAGT | 9690 |
rs2023974 | snp | C/T | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157219501 | CCCCTATGTTTCCTG[C/T]AATTTTGTAGTTAGA | 9690 |
rs2023975 | snp | C/T | 0.499999 | 0.000798721 | intron-variant | UBE3C | GRCh38.p7 | 7:157219402 | CGATCACTGAGAGGC[C/T]CCATCTCTGCTTTTC | 9690 |
rs2023976 | snp | C/T | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157219248 | CTGACATTTTCCCAT[C/T]GCACAACTTTCTGGA | 9690 |
rs2023977 | snp | C/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157203328 | AGACAGTAAATCATT[C/G]TAGGAGTCTTTTGTC | 9690 |
rs2051876 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157216343 | AAAAAACCCACGAAT[C/T]TGGAAATGTCTTAGC | 9690 |
rs2051877 | snp | A/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157216119 | GTCAGATCTGTGATC[A/T]TAACTCCAGAAAAAT | 9690 |
rs2107863 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157171037 | ATCACTTGAGGCTAG[A/G]AGTTCACGACCAGCC | 9690 |
rs2240399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157267167 | caaagtgctgggatt[A/G]caggcgtgagccacc | 9690 |
rs2286129 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157197974 | CAAGAATACATAAAA[C/T]CTAGATTGAGGTTCA | 9690 |
rs2286130 | snp | A/G | 0.384209 | 0.210922 | intron-variant | UBE3C | GRCh38.p7 | 7:157197860 | AAATCAATACTTAAC[A/G]CGGTTGTTCTTATTG | 9690 |
rs2286131 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157197794 | TTAGCAGATGGGAGT[C/T]GTTTGATACAAAGAT | 9690 |
rs2286132 | snp | C/T | 0.332799 | 0.23589 | intron-variant | UBE3C | GRCh38.p7 | 7:157197468 | TAAATTTTGGTTTTA[C/T]TGTTATTCTGTCTTC | 9690 |
rs2301913 | snp | A/G | 0.0057448 | 0.053286 | intron-variant | UBE3C | GRCh38.p7 | 7:157207573 | GCCAGCAGCAAACTG[A/G]TTTCTCAAAATCCTT | 9690 |
rs2301914 | snp | A/G | 0.481021 | 0.0955465 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207482 | CAAGGAGCTAAAAAG[A/G]TAAAAGAGTGGGATG | 9690 |
rs2301915 | snp | A/G | 0.332337 | 0.236052 | intron-variant | UBE3C | GRCh38.p7 | 7:157201617 | ACACTGAAGATCAAC[A/G]TACAATTTAGCAAAT | 9690 |
rs2301916 | snp | A/C | 0.498964 | 0.02274 | intron-variant | UBE3C | GRCh38.p7 | 7:157181433 | TTAAATGCTTTTAAC[A/C]ATCTCTACAGGTCCA | 9690 |
rs2301946 | snp | C/T | 0.353803 | 0.227431 | intron-variant | UBE3C | GRCh38.p7 | 7:157257115 | AGGACTTCATTTAAC[C/T]CTACTGAATGTTCTG | 9690 |
rs2301947 | snp | A/G | 0.355954 | 0.226437 | intron-variant | UBE3C | GRCh38.p7 | 7:157231027 | TTACAAGCAAGCAAT[A/G]ACATCAACTAGCCTT | 9690 |
rs2366214 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157199767 | tgatccaccaggtcc[A/G]gccATATTTCAGAGT | 9690 |
rs2366215 | snp | G/T | 0.332337 | 0.236052 | intron-variant | UBE3C | GRCh38.p7 | 7:157199996 | GGAATGAATGCAGTG[G/T]GCCCCCACTTTGTCA | 9690 |
rs2527876 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230711 | AACATTAGGAGGTTT[C/T]TTTTTTTTTTTTTTT | 9690 |
rs2706167 | snp | G/T | 0.426035 | 0.177515 | intron-variant | UBE3C | GRCh38.p7 | 7:157242517 | TGAGCCTGAGTTGTT[G/T]TTTTTTTTTTTTTTT | 9690 |
rs2706168 | snp | A/T | 0.489796 | 0.070696 | intron-variant | UBE3C | GRCh38.p7 | 7:157224794 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 9690 |
rs3039755 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169373 | TTTTTTTTTTTTTTT[-/TT]AAATTGAGACTGAGT | 9690 |
rs3039776 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201659 | ttttttttttttttt[A/T]AGAAATGTTTTGAAT | 9690 |
rs3039783 | in-del | -/AGAGA/AGAGAG | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157211194 | gagagagagagagag[-/AGAGA/AGAGAG]CCATACTATGAGTGA | 9690 |
rs3757827 | snp | A/G | 0.310632 | 0.242536 | intron-variant | UBE3C | GRCh38.p7 | 7:157265522 | AATGAATACGTACCT[A/G]GTTTTCACAGTTGTG | 9690 |
rs3757828 | snp | A/G | 0.122411 | 0.214991 | intron-variant | UBE3C | GRCh38.p7 | 7:157260557 | TACCGATAAAAAGTC[A/G]TCTGCACGCCTCACC | 9690 |
rs3757829 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157260549 | AAAAGTCGTCTGCAC[A/G]CCTCACCTGCAGTCC | 9690 |
rs3757830 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE3C | GRCh38.p7 | 7:157227296 | CAGCACCCGTGCCCT[C/T]GGAGCTCCCCTCACC | 9690 |
rs3757831 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157180582 | CATATACAAGCGTAT[A/T]TGGTAGCACATTAAA | 9690 |
rs3779593 | snp | A/G | 0.310386 | 0.242597 | intron-variant | UBE3C | GRCh38.p7 | 7:157261073 | TCAGGGGATCCACCC[A/G]CCTTGGCCTCCCAAA | 9690 |
rs3779596 | snp | C/T | 0.347032 | 0.230401 | intron-variant | UBE3C | GRCh38.p7 | 7:157243133 | CTCCTGTCCTATTTT[C/T]CTCATAGTGGCTTCC | 9690 |
rs3779598 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157238164 | ATAAAATTAACACCA[C/T]ATACCTTCATTTGGC | 9690 |
rs3779599 | snp | G/T | 0.483852 | 0.0883933 | intron-variant | UBE3C | GRCh38.p7 | 7:157238000 | TGGTGGTGCCATCAC[G/T]GCTCACTGCAGCCTC | 9690 |
rs3779603 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196755 | tctcaaactcccgac[C/T]tcaggtgatccaccc | 9690 |
rs3779604 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157149762 | AGTCACAGAGTGAAG[C/T]TCCTTACAGCTTTTG | 9690 |
rs3802103 | snp | C/T | 0.139903 | 0.224452 | intron-variant | UBE3C | GRCh38.p7 | 7:157265773 | CAACCAACGCTTCAG[C/T]GTCTTAAGTGCTCCC | 9690 |
rs3802106 | snp | C/T | 0.35574 | 0.226537 | intron-variant | UBE3C | GRCh38.p7 | 7:157236422 | AAATTTTCAAATATA[C/T]AACCAAGATCATATC | 9690 |
rs3802108 | snp | A/C | 0.349452 | 0.229367 | intron-variant | UBE3C | GRCh38.p7 | 7:157228372 | CTTTACAATTCTTAC[A/C]GCAATCCCATGAGGG | 9690 |
rs3802111 | snp | A/T | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157212189 | TTTCTACAGTAGATC[A/T]AGTCCTGAAACCAGA | 9690 |
rs3802113 | snp | C/T | 0.332337 | 0.236052 | intron-variant | UBE3C | GRCh38.p7 | 7:157208943 | TGTGCGAGAGGTCGC[C/T]GGTATTAAACGGACT | 9690 |
rs3802114 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157204954 | TCTTGAGAACAAGGG[C/T]TTTCAAATTGCGTGC | 9690 |
rs3802115 | snp | A/G | 0.464523 | 0.128375 | intron-variant | UBE3C | GRCh38.p7 | 7:157203534 | TCTGTTGCTAAGCTG[A/G]GGCACTTATGGGTAA | 9690 |
rs3802117 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157194306 | AACTACCACAGGATG[A/G]AAGTGGTGAGCCCAC | 9690 |
rs3802118 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157194120 | TCAAAATCATCTTCC[A/G]AAGAAAATGATTTCT | 9690 |
rs3802119 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188808 | AATACTTTTTTAAAA[A/C]AATCAAAATTGAAAG | 9690 |
rs3802120 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157185100 | AATTCTATGGGAGGT[A/G]ACTATTTAATAACTT | 9690 |
rs3802121 | snp | C/T | 0.460925 | 0.134204 | intron-variant | UBE3C | GRCh38.p7 | 7:157179837 | AAAAATAGTAACACG[C/T]CAAGCAGCAAGGCTG | 9690 |
rs3802122 | snp | A/T | 0.475965 | 0.106957 | intron-variant | UBE3C | GRCh38.p7 | 7:157179604 | CTTCTCGAGCCCAGG[A/T]GTCCTGAAGTGCTTG | 9690 |
rs3802123 | snp | C/T | 0.490175 | 0.0693959 | intron-variant | UBE3C | GRCh38.p7 | 7:157177947 | CTGTTTTTCCTTTTT[C/T]TTAAAAAAAAAAAAA | 9690 |
rs3802124 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157177915 | ACAGAATCCATCTGA[C/T]CACACATCACCTTTA | 9690 |
rs3802125 | snp | G/T | 0.498277 | 0.0293024 | intron-variant | UBE3C | GRCh38.p7 | 7:157177869 | GGCTGTTTCAATGCC[G/T]CACTGAAACTAACTT | 9690 |
rs3802126 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | UBE3C | GRCh38.p7 | 7:157177587 | CGAGTGCAGGAGGAG[C/T]GGGGCTACACATAAC | 9690 |
rs3802128 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157172870 | CCTCACTCAAAGGCA[A/G]TAGGTGCTCTGGAGA | 9690 |
rs3802129 | snp | C/T | 0.499598 | 0.0141716 | intron-variant | UBE3C | GRCh38.p7 | 7:157172603 | ACTGGCTCTCAGTTC[C/T]TTCTCTGCACGTTCT | 9690 |
rs3802130 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157172543 | ACCTTAGCTCAACTC[C/T]GGAGGCAATGCTGGG | 9690 |
rs3802131 | snp | A/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157151653 | CTCAAAAAAGCCCAG[A/T]AGAACCATAAGGAGT | 9690 |
rs3802132 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157151304 | CTACTGATACAGAAG[A/G]TAAGAGGTAAGAAGG | 9690 |
rs3802133 | snp | A/G | 0.328382 | 0.237395 | intron-variant | UBE3C | GRCh38.p7 | 7:157143937 | CTCTCCTCCACTCCC[A/G]GAGGTGTGACTCTTT | 9690 |
rs3808316 | snp | C/G | 0.499897 | 0.00718776 | intron-variant | UBE3C | GRCh38.p7 | 7:157152093 | CTCCATGGTTGGACA[C/G]CTTTGCCCATGCTGT | 9690 |
rs3808317 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157151766 | AAAATCATTGACTCC[C/T]CTTGGTCCAATTGCA | 9690 |
rs3815217 | snp | C/T | 0.474272 | 0.110462 | intron-variant | UBE3C | GRCh38.p7 | 7:157184287 | AACTAAGTTAACATA[C/T]AGTATGATCCTATTT | 9690 |
rs3824057 | snp | A/C | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157229254 | GCTCTGATAAACAGG[A/C]TGAATCAGAGAACAG | 9690 |
rs3824058 | snp | C/T | 0.34659 | 0.230587 | intron-variant | UBE3C | GRCh38.p7 | 7:157226849 | TAGGCAAGACAAACC[C/T]GGCCCTGTGGAGAGG | 9690 |
rs3824059 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157204728 | TCAAGGGATGCCTAA[C/T]GGAAAACAGTACCAG | 9690 |
rs3824060 | snp | A/G | 0.375 | 0.216506 | intron-variant | UBE3C | GRCh38.p7 | 7:157192358 | CTGCATTTTGGTGGC[A/G]GCTCCACCGCAGATG | 9690 |
rs3824061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157180192 | AATAATGGTAATACT[A/G]TAATTTAAAAGGCTA | 9690 |
rs3824062 | snp | C/T | 0.329084 | 0.237162 | intron-variant | UBE3C | GRCh38.p7 | 7:157155844 | TGCTGTAACTACCCA[C/T]CAATGTGAAATCCAC | 9690 |
rs3834361 | in-del | -/TTTTAATGGT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180577 | ACAAGCGTATTTGGT[-/TTTTAATGGT]AGCACATTAAAAACA | 9690 |
rs3834362 | in-del | -/AA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180340 | TCAAGAATTTTAAAA[-/AA]TACACAGAGACTTTT | 9690 |
rs3837146 | in-del | -/A | 0.386123 | 0.209692 | intron-variant | UBE3C | GRCh38.p7 | 7:157246230 | TACTTCGTATGTGTA[-/A]GTCTATAAAATGCGC | 9690 |
rs3837147 | in-del | -/T/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237887 | TTTTTTTTTTTTTTT[-/T/TT]AGTGGTAGAGACCAG | 9690 |
rs3837148 | in-del | -/C | 0.493247 | 0.0577133 | intron-variant | UBE3C | GRCh38.p7 | 7:157196754 | CTCAAACTCCCGACC[-/C]TCAGGTGATCCACCC | 9690 |
rs3839845 | in-del | -/CTG | 0.498611 | 0.0263212 | intron-variant | UBE3C | GRCh38.p7 | 7:157193287 | TAATTTGTTCTTCTG[-/CTG]AAATTTTTCTTTTTA | 9690 |
rs3839846 | in-del | -/A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188812 | TTCAAATACTTTTTT[-/A/T]AAAAAAATCAAAATT | 9690 |
rs3839847 | in-del | -/A | 0.257732 | 0.24988 | intron-variant | UBE3C | GRCh38.p7 | 7:157188805 | ACTTTTTTAAAAAAA[-/A]TCAAAATTGAAAGCA | 9690 |
rs3839848 | in-del | -/TTAG | 0.32955 | 0.237006 | intron-variant | UBE3C | GRCh38.p7 | 7:157188770 | TAAAATCTGTAACAG[-/TTAG]AGTAAGCCTACTTGC | 9690 |
rs3839849 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157179689 | GCTGCTTATAATTCT[-/T]GTCTGCAGCCACGGC | 9690 |
rs3839850 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177930 | taaaaaaaaaaaaaa[-/A]CAGAATCCATCTGAC | 9690 |
rs4257905 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171688 | tatatatatatatat[A/T]tTTTTTttttttttt | 9690 |
rs4262225 | snp | A/C | 0.118933 | 0.212888 | intron-variant | UBE3C | GRCh38.p7 | 7:157267134 | AATTTTTTAAAAAAG[A/C]AAATGTGGGCCAGGC | 9690 |
rs4716458 | snp | A/G | 0.329084 | 0.237162 | intron-variant | UBE3C | GRCh38.p7 | 7:157151107 | GTCCAGCCCACTCTC[A/G]GGGTGAGGGGAGTCG | 9690 |
rs4716459 | snp | A/G | 0.329783 | 0.236927 | intron-variant | UBE3C | GRCh38.p7 | 7:157177290 | ATACTGGTCACTCAG[A/G]TGGCTCTTTTTCAAG | 9690 |
rs4716460 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | UBE3C | GRCh38.p7 | 7:157177360 | TGTCTCTTGACAATA[C/T]GGATATCCTTTTCCC | 9690 |
rs4716461 | snp | C/T | 0.332568 | 0.235971 | intron-variant | UBE3C | GRCh38.p7 | 7:157191587 | GCAGGTGCAAGTCAC[C/T]GCGCCCAGCCCCTCG | 9690 |
rs4716690 | snp | A/G | 0.329783 | 0.236927 | intron-variant | UBE3C | GRCh38.p7 | 7:157167601 | GGAATGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 9690 |
rs4716691 | snp | A/G | 0.464947 | 0.127663 | intron-variant | UBE3C | GRCh38.p7 | 7:157167727 | ATTTTTAGAAGAGGT[A/G]TGGTTTCACCATTTT | 9690 |
rs4716692 | snp | A/T | 0.464947 | 0.127663 | intron-variant | UBE3C | GRCh38.p7 | 7:157167728 | TTTTTAGAAGAGGTA[A/T]GGTTTCACCATTTTA | 9690 |
rs4716693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157189675 | TTCCTGACTCTTTCA[C/G]CGGCTTCTTTCATAG | 9690 |
rs5888710 | in-del | -/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157171121 | ATGATTTAGGGTCTC[-/T]TTTTGTGGGGAGGGC | 9690 |
rs6459733 | snp | C/G | 0.496348 | 0.0425753 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137856 | ggcgtgagcgaccgt[C/G]ctcggccgcaggacg | 9690 |
rs6459734 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157142760 | GCTCACTCCCCGGGT[A/G]ATGGGATCATTCACA | 9690 |
rs6459735 | snp | C/G | 0.387263 | 0.208947 | intron-variant | UBE3C | GRCh38.p7 | 7:157142787 | cacaccccaaacctc[C/G]gcgtcctgcagtata | 9690 |
rs6459736 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157172909 | CTTAGTCATCAGTCA[C/T]GACATGGTGTAGCTA | 9690 |
rs6459737 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | UBE3C | GRCh38.p7 | 7:157182442 | TGGGCCTCTCCTGGA[A/G]GAGTGTATTTGCTGG | 9690 |
rs6459738 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157205838 | CACATATGGGTTCCT[G/T]TTCTCAAAGCGGTTG | 9690 |
rs6459739 | snp | A/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157206169 | AGCCTATTAGCTAAA[A/T]GTTCCATAAGACAAG | 9690 |
rs6459740 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157216165 | GAGGCAAGTGCTGCA[A/G]TTGTTTTCTCTTTGG | 9690 |
rs6459741 | snp | G/T | 0.49941 | 0.0171624 | intron-variant | UBE3C | GRCh38.p7 | 7:157221859 | atttgttTTTTTGTT[G/T]TGttttcttggttgt | 9690 |
rs6459742 | snp | A/G | 0.474813 | 0.109357 | intron-variant | UBE3C | GRCh38.p7 | 7:157234290 | gtatgttcttctgac[A/G]gtgttgtagttttag | 9690 |
rs6459743 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | UBE3C | GRCh38.p7 | 7:157234414 | tagttgaccgtacac[A/G]taacactctgggtct | 9690 |
rs6459744 | snp | A/G | 0.268995 | 0.249277 | intron-variant | UBE3C | GRCh38.p7 | 7:157234607 | TTGAAATGCATTGTC[A/G]TAGCCCCAGTTATTT | 9690 |
rs6459745 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157238494 | agatgttgggatgtg[C/T]gaggacaggagaagg | 9690 |
rs6459746 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157238534 | cacctgggttctgtt[A/G]tgagaactagaagga | 9690 |
rs6459747 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157238871 | agggagaaaaccaga[A/G]aagtgggatttcagg | 9690 |
rs6459749 | snp | C/T | 0.184203 | 0.241186 | intron-variant | UBE3C | GRCh38.p7 | 7:157263391 | TTACAGAAAGTCGAA[C/T]GGGggccgggtgtgg | 9690 |
rs6943921 | snp | A/G | 0.332568 | 0.235971 | intron-variant | UBE3C | GRCh38.p7 | 7:157208467 | TTCATTTTAATTTAC[A/G]TTTGCCTCACTTAAA | 9690 |
rs6946660 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157155954 | TGCTACTAGGCATCC[C/T]TACGGGTTCTACATC | 9690 |
rs6946713 | snp | C/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157235886 | AACCATTGCTCGGAT[C/G]TAAGTAAGTGTCATA | 9690 |
rs6946947 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157156093 | TCTCCTGGTACCTTA[C/T]TTGCCCCTTTCCTCC | 9690 |
rs6947927 | snp | A/G | 0.46014 | 0.13543 | intron-variant | UBE3C | GRCh38.p7 | 7:157218174 | ATGTCggctgggcgc[A/G]gtggctcatgcctgt | 9690 |
rs6949120 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157211670 | GCTATATAAAATTTG[G/T]TTAACCCTTGACAGC | 9690 |
rs6949802 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | UBE3C | GRCh38.p7 | 7:157236186 | TCGCCTGTAAGTCAG[A/G]CTGCAGACAGGGAAT | 9690 |
rs6950215 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157262986 | GAACATAAACTCAAG[A/C]TTGTATTGTCTTCAT | 9690 |
rs6950377 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | UBE3C | GRCh38.p7 | 7:157172800 | CTAATCTTGTAGATT[A/G]CAAGATCACCAAGGA | 9690 |
rs6950641 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | UBE3C | GRCh38.p7 | 7:157236665 | ATACTAGTCATTTTG[A/G]TTGCCTTAGTCCTTA | 9690 |
rs6950739 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | UBE3C | GRCh38.p7 | 7:157189756 | GTGGGTTCTTTTTTC[C/T]CCTCTTTCTCACTCT | 9690 |
rs6951298 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157156455 | GGGACTACAGGCGCA[C/T]GTCACCACCCCCGGC | 9690 |
rs6951367 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157176223 | gctgtgattgtgcta[C/T]tgaactccagtttgg | 9690 |
rs6951930 | snp | A/G | 0.334412 | 0.235318 | intron-variant | UBE3C | GRCh38.p7 | 7:157190637 | AGAGCTGTATTCTCT[A/G]TGTCATGGTTTGCCA | 9690 |
rs6954050 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157185860 | GCTTTTATCTATAAA[A/G]CAGTGTTTTGTTTGG | 9690 |
rs6955056 | snp | G/T | 0.32885 | 0.23724 | intron-variant | UBE3C | GRCh38.p7 | 7:157212888 | TCGGCCTCCTGAGTA[G/T]CTGGGACTACAGGCA | 9690 |
rs6955184 | snp | G/T | 0.26326 | 0.249648 | intron-variant | UBE3C | GRCh38.p7 | 7:157197345 | TGTAACAAACTGATT[G/T]GCCTACAAATCCAAA | 9690 |
rs6955670 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | UBE3C | GRCh38.p7 | 7:157237398 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 9690 |
rs6955689 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157237436 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAGA | 9690 |
rs6956046 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157170180 | CTGTGAGCAAGGACC[A/G]ATAATGGTGTTTTCG | 9690 |
rs6956612 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157177763 | CAGAAGGCAGCCTGC[A/G]GTAAGCGGATAAGCC | 9690 |
rs6956786 | snp | C/T | 0.26818 | 0.249338 | intron-variant | UBE3C | GRCh38.p7 | 7:157237365 | agaatggcgtgaacc[C/T]gggaggcggagcttg | 9690 |
rs6957939 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157185791 | CCTTTCTCATTCTGA[C/T]GTACTTTTGTTAGTC | 9690 |
rs6958472 | snp | A/G | 0.0418186 | 0.138422 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138064 | gatatatatgtatat[A/G]cacatgtatatgaga | 9690 |
rs6958485 | snp | A/G | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138078 | tgcacatgtatatga[A/G]atattatgtatacgt | 9690 |
rs6960676 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | UBE3C | GRCh38.p7 | 7:157238223 | AGGCGGCAGTAAGTA[A/G]AGTGGTGGAGGTCAC | 9690 |
rs6961733 | snp | A/C/T | 0.0521138 | 0.152927 | intron-variant | UBE3C | GRCh38.p7 | 7:157158247 | AAGGAAACACAAATA[A/C/T]AATGAAGCCTTTTGA | 9690 |
rs6961953 | snp | C/T | 0.268995 | 0.249277 | intron-variant | UBE3C | GRCh38.p7 | 7:157238274 | AGTGGGGACTCCTGG[C/T]GTCACCAGCAGAGGG | 9690 |
rs6962133 | snp | C/T | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157238392 | GATGGAGTGTCACAT[C/T]GTTCAGGTGGAGTGA | 9690 |
rs6962804 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | UBE3C | GRCh38.p7 | 7:157231559 | cagtgtgccagtatt[C/G]agaggtggaatcttt | 9690 |
rs6965963 | snp | C/T | 0.148661 | 0.22854 | intron-variant | UBE3C | GRCh38.p7 | 7:157149391 | AAAATAGAAACCAAG[C/T]GGAATGGAAGGAGTG | 9690 |
rs6965998 | snp | A/T | 0.148326 | 0.228391 | intron-variant | UBE3C | GRCh38.p7 | 7:157235721 | AATAACAAAACTAAG[A/T]GTAATTTGAGGATGG | 9690 |
rs6966805 | snp | C/T | 0.11963 | 0.213316 | intron-variant | UBE3C | GRCh38.p7 | 7:157252956 | TGCTTTATCTCAAAC[C/T]CCTGGGCTTAAGGGA | 9690 |
rs6967012 | snp | G/T | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157144798 | ttttctctattacta[G/T]catctggcattaatg | 9690 |
rs6967764 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157202270 | CTTAACATATTTTAA[C/T]TGAGTATGTAATAGG | 9690 |
rs6969244 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | UBE3C | GRCh38.p7 | 7:157211318 | TAATCCTAACATGCG[A/G]CCATTTGACTATGTT | 9690 |
rs6970923 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157176125 | TGATATATGTAAATA[G/T]AATTATTCTTTTCCC | 9690 |
rs6971669 | snp | A/T | 0.180702 | 0.240204 | intron-variant | UBE3C | GRCh38.p7 | 7:157259844 | GGATAATCTTATAGT[A/T]AGTCAAGTACACCTC | 9690 |
rs6971896 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157185718 | TAATCTGTTCACTTA[C/T]AGCTTATGTACAATT | 9690 |
rs6972035 | snp | A/G | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157142146 | atgttgagcacctac[A/G]tatgcttgttttcct | 9690 |
rs6972058 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157185822 | TTAATGTTAAAGATT[C/T]AGGTTTGACAGATGA | 9690 |
rs6972626 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170141 | tttttttttcttttt[A/T]ACCATTTTTTTTCTA | 9690 |
rs6975954 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | UBE3C | GRCh38.p7 | 7:157237217 | GAGGCCGAGGTGGGC[A/G]GATCACCAGGTCAGG | 9690 |
rs6977058 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157237895 | ctaccactaaaaaaa[A/G]aaaaaaagtagccag | 9690 |
rs6977096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246750 | GACAGTAGGAAGGCC[C/T]GTGACTGCCTCTGTT | 9690 |
rs6977213 | snp | A/G | 0.106987 | 0.205054 | intron-variant | UBE3C | GRCh38.p7 | 7:157177785 | GGATAAGCCGTGTAG[A/G]CACACCCCACCCAGA | 9690 |
rs6977324 | snp | C/G | 0.474091 | 0.11083 | intron-variant | UBE3C | GRCh38.p7 | 7:157146490 | CGTCCCAAAGTGCTG[C/G]GATTACAGGCATGAG | 9690 |
rs6977680 | snp | A/G | 0.49823 | 0.0296997 | intron-variant | UBE3C | GRCh38.p7 | 7:157146724 | CAGTGTTGTGACCTC[A/G]GCTCACTGCAAACTC | 9690 |
rs6977962 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | UBE3C | GRCh38.p7 | 7:157234733 | ATCTTCAGGCTCACC[A/G]TATTTCAGGTGGCAG | 9690 |
rs6979947 | snp | A/G | 0.49645 | 0.0419827 | intron-variant | UBE3C | GRCh38.p7 | 7:157213169 | GAGAGGAGGCACAAG[A/G]GTTAACACATCAGAT | 9690 |
rs7384424 | snp | A/G | 0.239037 | 0.24976 | intron-variant | UBE3C | GRCh38.p7 | 7:157254955 | tcccggcgtggtggc[A/G]tacacctgcagtccc | 9690 |
rs7777431 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187561 | taattttttgttttt[G/T]tgtGTGTGTGTGttt | 9690 |
rs7777476 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157187645 | cagtggcgcgatctc[A/G]gctcactgtaggctc | 9690 |
rs7777654 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | UBE3C | GRCh38.p7 | 7:157230998 | CCTCACACCCCTTCC[C/T]TAAGCCTTCCTGTAA | 9690 |
rs7778050 | snp | A/G | 0.154661 | 0.231107 | intron-variant | UBE3C | GRCh38.p7 | 7:157188003 | TTAAAAATATGGCCT[A/G]TTTGTGCTTAAATAA | 9690 |
rs7778193 | snp | C/T | 0.499879 | 0.0077866 | intron-variant | UBE3C | GRCh38.p7 | 7:157187393 | GGGGTTTTTTTTTTT[C/T]TTCTTCTTCTTCAGA | 9690 |
rs7784143 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | UBE3C | GRCh38.p7 | 7:157141567 | tcttcatgcaatggt[A/G]agtgtctgtgcatcc | 9690 |
rs7784158 | snp | C/T | 0.383246 | 0.211531 | intron-variant | UBE3C | GRCh38.p7 | 7:157154119 | acgaggtcaggagtt[C/T]agaccagtctggcca | 9690 |
rs7784442 | snp | C/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157141781 | cactcaccacttgtc[C/G]tttgtgcccggctgc | 9690 |
rs7784588 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | UBE3C | GRCh38.p7 | 7:157141181 | cttagtaggaactgg[C/T]agcagctggggcatg | 9690 |
rs7784779 | snp | C/T | 0.148996 | 0.228688 | intron-variant | UBE3C | GRCh38.p7 | 7:157149236 | taatttttctatttt[C/T]agtagagatgggttt | 9690 |
rs7784782 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | UBE3C | GRCh38.p7 | 7:157206325 | tggagtgcaatggca[C/T]gatctcggctcactg | 9690 |
rs7784795 | snp | C/T | 0.329317 | 0.237084 | intron-variant | UBE3C | GRCh38.p7 | 7:157206348 | GCTCACTGCAACCTC[C/T]GCTGCTCGGGTTCAA | 9690 |
rs7785227 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | UBE3C | GRCh38.p7 | 7:157206603 | TAATATTTTAAACTT[C/T]TTTGAAACAGAGTCT | 9690 |
rs7785599 | snp | A/G | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157190814 | TTTATTTCTAGCACA[A/G]AATACTTTTTCTCCA | 9690 |
rs7786095 | snp | A/G | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157191153 | ACCAAAAAGTAGTAC[A/G]GTGAAGCAGCTTAAT | 9690 |
rs7789863 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150161 | ggctggcagatcact[C/T]gaggtcaggagttcc | 9690 |
rs7790880 | snp | C/T | 0.477853 | 0.102875 | intron-variant | UBE3C | GRCh38.p7 | 7:157142897 | TCGCTCACGCTGGAG[C/T]GCAGTGTTGCCCAGG | 9690 |
rs7794035 | snp | C/T | 0.399968 | 0.200024 | intron-variant | UBE3C | GRCh38.p7 | 7:157183527 | ccttggaagttggtg[C/T]gtggggctgaaagtt | 9690 |
rs7794202 | snp | C/T | 0.15698 | 0.23205 | intron-variant | UBE3C | GRCh38.p7 | 7:157251730 | GAAATTTTAAATATG[C/T]CCCTCAGATCTGAAA | 9690 |
rs7798305 | snp | C/T | 0.140581 | 0.224783 | intron-variant | UBE3C | GRCh38.p7 | 7:157189961 | ACCCATCACCATGCC[C/T]AGCTAATTTTTGTAT | 9690 |
rs7798748 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157184995 | GCATCTGTCCAAACT[G/T]TACACCAACAAGTAT | 9690 |
rs7798816 | snp | A/G | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157147880 | gtcttgcgtatctgg[A/G]ataaatcccacttga | 9690 |
rs7800888 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187586 | GTGtttgttttttgt[G/T]tttttttttgagatg | 9690 |
rs7801905 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157147417 | tcttagttccaggag[C/T]ggttttttggttgat | 9690 |
rs7802642 | snp | A/G | 0.418306 | 0.18486 | intron-variant | UBE3C | GRCh38.p7 | 7:157188978 | TGTGGAGACCTTTGT[A/G]CCCTGACATGGAAAG | 9690 |
rs7804018 | snp | C/T | 0.387263 | 0.208947 | intron-variant | UBE3C | GRCh38.p7 | 7:157150582 | catttgttaaataac[C/T]gttaatataacaatg | 9690 |
rs7806314 | snp | A/T | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157154209 | ggctgtaatcccagc[A/T]acttgggagactgag | 9690 |
rs7806672 | snp | A/G | 0.386884 | 0.209196 | intron-variant | UBE3C | GRCh38.p7 | 7:157259023 | agacagttttgaaac[A/G]gccacaattaaatta | 9690 |
rs7806775 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157154505 | tcacctcaacaaaat[A/G]tcttagtgattccat | 9690 |
rs7807556 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | UBE3C | GRCh38.p7 | 7:157141635 | tgggaccacggtgta[C/T]atgtggtctgttgtc | 9690 |
rs7807856 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157141804 | ccggctgctttggct[C/T]GGCTTCTGTCTGAGA | 9690 |
rs7809255 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157142874 | ttttttttttttgag[A/T]tggagtttcgctcac | 9690 |
rs7811640 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE3C | GRCh38.p7 | 7:157192533 | GAAGATGGATGTACT[A/G]TCTGACTACAACATT | 9690 |
rs7811779 | snp | A/G | 0.160938 | 0.233598 | intron-variant | UBE3C | GRCh38.p7 | 7:157243283 | GAGTGCCAGGGTCTC[A/G]AGGAAGAAAAGGTAC | 9690 |
rs9771361 | snp | A/C | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157246879 | TAAATACACATCTCT[A/C]TGAAGACTGGATAtt | 9690 |
rs9918649 | snp | C/T | 0.000560021 | 0.0167241 | intron-variant | UBE3C | GRCh38.p7 | 7:157267559 | TGCTTGTTACAGTGA[C/T]ATCTTGCACACATGC | 9690 |
rs9918721 | snp | A/G/T | 0.0185083 | 0.0944024 | intron-variant | UBE3C | GRCh38.p7 | 7:157267571 | TGACATCTTGCACAC[A/G/T]TGCTGTTTTTCAGGA | 9690 |
rs9918723 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157167119 | tatttttagtagaga[C/T]ggagtttcaccatgt | 9690 |
rs10085650 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | UBE3C | GRCh38.p7 | 7:157200719 | GGCTCACTGCAGCCT[C/T]GAACTCCTGGGCTCT | 9690 |
rs10224221 | snp | C/T | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157177512 | ACATGCTGCTGACTT[C/T]TCCAGGTTGACAAGA | 9690 |
rs10224496 | snp | A/G | 0.344592 | 0.231414 | intron-variant | UBE3C | GRCh38.p7 | 7:157213968 | TATTATTTGATATAA[A/G]TAAATATAAACATAT | 9690 |
rs10225989 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157175358 | ACTCCTGATGTGTGA[A/G]AATGATTCCATTCCA | 9690 |
rs10227115 | snp | A/G | 0.330016 | 0.236849 | intron-variant | UBE3C | GRCh38.p7 | 7:157165553 | caggtgcacgccacc[A/G]cacccagctaatttt | 9690 |
rs10228143 | snp | A/G | 0.329783 | 0.236927 | intron-variant | UBE3C | GRCh38.p7 | 7:157184555 | TGTTTTACTTAAAGA[A/G]TTTAACCGCCAATGA | 9690 |
rs10228145 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | UBE3C | GRCh38.p7 | 7:157214643 | ATGGAAAGACCAGAC[A/G]CGAACATCTTCATAC | 9690 |
rs10228373 | snp | A/C | 0.349452 | 0.229367 | intron-variant | UBE3C | GRCh38.p7 | 7:157244898 | GATATGCTTCTAGGA[A/C]CAAGCGTGGTACAGC | 9690 |
rs10228507 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157184855 | GGCTTGATTTTTTTT[A/T]AAAAATAAGAGAAGA | 9690 |
rs10229630 | snp | A/G | 0.499999 | 0.000599041 | intron-variant | UBE3C | GRCh38.p7 | 7:157212096 | TGTATTTCCCACATT[A/G]CACATTTATTGCACT | 9690 |
rs10230895 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157214344 | GAAAATATATGTTCT[C/T]ATGAACAGAGATTGA | 9690 |
rs10231434 | snp | A/G | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157166728 | ctggagtgaaactcc[A/G]tctcaaaaaaaaaaa | 9690 |
rs10231648 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157166941 | ggtggtggtggtggt[G/T]gtttttgagacaaag | 9690 |
rs10233206 | snp | A/G | 0.138886 | 0.22395 | intron-variant | UBE3C | GRCh38.p7 | 7:157242774 | AAAAAAGGAAGGGTC[A/G]AGCCAGGTCTGGTGG | 9690 |
rs10237192 | snp | G/T | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157183372 | cacagaactcgggaa[G/T]Tcgaggtgtgcggga | 9690 |
rs10238391 | snp | A/G | 0.0689305 | 0.172377 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268662 | TTTCCCCTGGGCTGC[A/G]CCCACTTGTCTTCCT | 9690 |
rs10239165 | snp | C/T | 0.148326 | 0.228391 | intron-variant | UBE3C | GRCh38.p7 | 7:157201192 | agccaggcgtggtgg[C/T]gggcacctgtaatcc | 9690 |
rs10240226 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBE3C | GRCh38.p7 | 7:157171926 | tgggcaggctggtct[C/T]gaactcctggcctca | 9690 |
rs10240474 | snp | C/T | 0.180702 | 0.240204 | intron-variant | UBE3C | GRCh38.p7 | 7:157256409 | gggcctcccaaagtg[C/T]tgggattacaggtgt | 9690 |
rs10245084 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157227631 | catgaacccgggagg[C/T]ggaggttgcagtgag | 9690 |
rs10246072 | snp | C/G | 0.331843 | 0.237885 | intron-variant | UBE3C | GRCh38.p7 | 7:157185792 | CTTTCTCATTCTGAT[C/G]TACTTTTGTTAGTCT | 9690 |
rs10250039 | snp | A/T | 0.470327 | 0.118136 | intron-variant | UBE3C | GRCh38.p7 | 7:157229928 | TTAAtttatttattt[A/T]ttttttttttgagac | 9690 |
rs10250482 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157254401 | TTTAATTAATTTATT[A/T]ATTTTTTTTTTTTCA | 9690 |
rs10250483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157254406 | TTAATTTATTTATTT[A/T]TTTTTTTTCAGACTG | 9690 |
rs10250518 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | UBE3C | GRCh38.p7 | 7:157170153 | tttAACCATTTTTTT[C/T]CTACAATTCAACTGT | 9690 |
rs10251112 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157170830 | AAACTCTAAAATACA[A/G]GGTCTCAGTGTTTAC | 9690 |
rs10252238 | snp | C/G | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157139592 | GGACTCGGGGCCTCC[C/G]TGGCTGGAACTCGAG | 9690 |
rs10254551 | snp | C/T | 0.356169 | 0.226336 | intron-variant | UBE3C | GRCh38.p7 | 7:157240195 | AAGTAACTGGGACTA[C/T]GGACACCCACCACCA | 9690 |
rs10256197 | snp | A/G | 0.347473 | 0.230215 | intron-variant | UBE3C | GRCh38.p7 | 7:157161794 | ACTTGATTCTAggcc[A/G]agcatggtgtctcat | 9690 |
rs10259021 | snp | A/C | 0.329783 | 0.236927 | intron-variant | UBE3C | GRCh38.p7 | 7:157202585 | TCGCTTAAACCTGGA[A/C]GGCGGAGGTTGCAGT | 9690 |
rs10259783 | snp | A/G | 0.353371 | 0.227628 | intron-variant | UBE3C | GRCh38.p7 | 7:157259700 | AGAGACACAGAGCGG[A/G]TCAGGGGCTGCACAG | 9690 |
rs10259984 | snp | A/G | 0.349452 | 0.229367 | intron-variant | UBE3C | GRCh38.p7 | 7:157227535 | AACCCTGTCTCTACT[A/G]AAAATACAAAAAAAA | 9690 |
rs10260754 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157228099 | TAATGTGATTATTCC[A/T]CGTGTCATCTAGTCA | 9690 |
rs10261274 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254928 | tcccagcgtggtggc[A/G]tacacctgcagtccc | 9690 |
rs10261278 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254944 | tacacctgcagtccc[A/G]gcgtggtggcgtaca | 9690 |
rs10261642 | snp | A/G | 0.440333 | 0.16209 | intron-variant | UBE3C | GRCh38.p7 | 7:157225121 | GATTCTCGTGCCTCA[A/G]CCTCCCAAGTAGCTG | 9690 |
rs10262763 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157242161 | CTGTTACAAAGGAAT[C/T]GTGCGGTAGGTAACG | 9690 |
rs10264206 | snp | A/G | 0.143959 | 0.226396 | intron-variant | UBE3C | GRCh38.p7 | 7:157230852 | CCCTGAGAGTTTGTg[A/G]gggcggaggttgcag | 9690 |
rs10264936 | snp | G/T | 0.495818 | 0.0455352 | intron-variant | UBE3C | GRCh38.p7 | 7:157157987 | AGATATATATATATA[G/T]AGAGAGAGAGAGAGA | 9690 |
rs10266129 | snp | A/G | 0.485866 | 0.0828688 | intron-variant | UBE3C | GRCh38.p7 | 7:157239693 | AGCTGTGTTCTAAAG[A/G]TGGGAGAAATAACAG | 9690 |
rs10266281 | snp | A/G | 0.349233 | 0.229462 | intron-variant | UBE3C | GRCh38.p7 | 7:157239848 | AAGAGGTAGAGGAAC[A/G]CTGGGTGCAGCTGCA | 9690 |
rs10266518 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | UBE3C | GRCh38.p7 | 7:157239996 | CCGGGGGATCTATTA[A/G]AAATGCAAATTCTTG | 9690 |
rs10267463 | snp | C/T | 0.332337 | 0.236052 | intron-variant | UBE3C | GRCh38.p7 | 7:157183428 | GGCACTCCACACTCT[C/T]GGCACCTCCCTGTGT | 9690 |
rs10268650 | snp | A/G | 0.170408 | 0.236992 | intron-variant | UBE3C | GRCh38.p7 | 7:157171800 | taacctccgcctcac[A/G]ggttcaagcgattct | 9690 |
rs10269105 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157179331 | GTCCTTTCACATTAG[C/T]TCAGTAGAAGAGAAT | 9690 |
rs10271970 | snp | A/C | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157205906 | AGACTCAGAAGCTCC[A/C]GGTGGCTCAGCCAAG | 9690 |
rs10271990 | snp | C/T | 0.354235 | 0.227234 | intron-variant | UBE3C | GRCh38.p7 | 7:157244827 | GACAGTTGAAAAATT[C/T]GTTACAGGTCTTTTC | 9690 |
rs10274687 | snp | G/T | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157140487 | TGCAGTTAAGGGTGG[G/T]CGTGGTAGCACTTAG | 9690 |
rs10280094 | snp | G/T | 0.33303 | 0.235809 | intron-variant | UBE3C | GRCh38.p7 | 7:157240094 | TTTTGGTTTTTTGGG[G/T]TTTTTTGAGACAGAG | 9690 |
rs10479650 | snp | A/G | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157176124 | ATGATATATGTAAAT[A/G]TAATTATTCTTTTCC | 9690 |
rs10488093 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | UBE3C | GRCh38.p7 | 7:157209713 | AAGATAAGCCTGTCA[C/T]GGAAATTATGAAACT | 9690 |
rs10534786 | in-del | -/TC | 0.492533 | 0.0606443 | intron-variant | UBE3C | GRCh38.p7 | 7:157189826 | TAGTTTGTGACGGAG[-/TC]TCTTGCCTTGTCGCC | 9690 |
rs10553043 | in-del | -/TAAAT | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269096 | TCTTAATTTGAATAA[-/TAAAT]TAAGCGTTTAAATGC | 9690 |
rs10553044 | in-del | -/GTT | 0.0275645 | 0.114116 | cds-indel, downstream-variant-500B, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269177 | TTTTTATTTTAGGTT[-/GTT]TTATGTTGAATGTTC | 9690 |
rs10570423 | in-del | -/GAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157142368 | TATAGATCTGTGTAC[-/GAC]AAGTCTGACTTGAAG | 9690 |
rs10598082 | in-del | -/GAGG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157154084 | CAGCACCTTGGGAGG[-/GAGG]CCGAGGTGGGTGGAT | 9690 |
rs10637384 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187381 | TCGTGTTTTATGGGG[-/TT]TTTTTTTTTTTTTTC | 9690 |
rs10648532 | in-del | -/CTTC | 0.0532157 | 0.154195 | intron-variant | UBE3C | GRCh38.p7 | 7:157234126 | GCAAGTATTTTCTTC[-/CTTC]TCTGGATTGTCTCTT | 9690 |
rs10678811 | in-del | -/AG | 0.499824 | 0.00938333 | intron-variant | UBE3C | GRCh38.p7 | 7:157206793 | CTCTTGATGGGTGAA[-/AG]AGGCTGCTGAGTAAA | 9690 |
rs10713758 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201658 | TTTTTTTTTTTTTTT[-/T]AAGAAATGTTTTGAA | 9690 |
rs10714296 | in-del | -/T | 0.333491 | 0.235646 | intron-variant | UBE3C | GRCh38.p7 | 7:157142855 | AAAATAAAAGTTGAA[-/T]TTTTTTTTTTTTTTT | 9690 |
rs10949635 | snp | G/T | 0.333952 | 0.235483 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138428 | CGTGTCATAGACATA[G/T]AACAGGTGGGATGTA | 9690 |
rs11278310 | in-del | -/GGCATGAG | 0.499853 | 0.008585 | intron-variant | UBE3C | GRCh38.p7 | 7:157170097 | AGTGCTGGGATTAAA[-/GGCATGAG]CCACCATGCCTGGTT | 9690 |
rs11297417 | in-del | -/G | 0.157311 | 0.232183 | intron-variant | UBE3C | GRCh38.p7 | 7:157251857 | GTTATTAGAGGGGCT[-/G]GGGCGCAGTGGCTCA | 9690 |
rs11350696 | in-del | -/A | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157223576 | TGATTGAAAGCCAGT[-/A]AACACTATAGATTTC | 9690 |
rs11370278 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157159324 | AAAAAAGAAAAGATT[-/A]AAAAAAAAAAAACAG | 9690 |
rs11373650 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216359 | TTCGTGGGTTTTTTT[-/T]TTTTTTAATATTTTA | 9690 |
rs11390914 | in-del | -/A/AA | 0.382473 | 0.212016 | intron-variant | UBE3C | GRCh38.p7 | 7:157186415 | CAAAAAAAAAAAAAA[-/A/AA]TTTATGTAATACTCT | 9690 |
rs11404789 | in-del | -/C | 0.326506 | 0.238006 | intron-variant | UBE3C | GRCh38.p7 | 7:157189754 | GTGGGTTCTTTTTTC[-/C]TCCTCTTTCTCACTC | 9690 |
rs11406459 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187589 | TTGTTTTTTGTTTTT[-/T]TTTTTTGAGATGGAG | 9690 |
rs11436417 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257743 | GAGACCCTGTCTCCA[-/A]AAAAAAAAAAAAAAA | 9690 |
rs11451004 | snp | A/T | 0.0312764 | 0.121078 | intron-variant | UBE3C | GRCh38.p7 | 7:157144690 | GTCCAGTGCTTTTTT[A/T]AAAAAAAAATAGACT | 9690 |
rs11765202 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227829 | TGATCACACCCACCT[C/G]CCTAGGGGCATGCTA | 9690 |
rs11767190 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187656 | tctcggctcactgta[A/G]gctctgcccccctgg | 9690 |
rs11771975 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157175201 | AATTTTTACTGTAGG[G/T]GATTCAGGCCGGCAT | 9690 |
rs11973570 | snp | A/G | 0.220246 | 0.248223 | intron-variant | UBE3C | GRCh38.p7 | 7:157191778 | ACAGATTTGTTTTTC[A/G]TTGTATGTGTAGAAT | 9690 |
rs11976909 | snp | A/T | 0.254944 | 0.249951 | intron-variant | UBE3C | GRCh38.p7 | 7:157229932 | tttatttattttttt[A/T]ttttttgagactgtc | 9690 |
rs11977140 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157224686 | CAAGAGTGTATTTTT[C/T]AGGCCTATACACTCT | 9690 |
rs11979099 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157199295 | CCGTATGACTGTTGC[A/G]TATTCTTAGCAAATA | 9690 |
rs11980541 | snp | C/G | 0.499801 | 0.00998203 | intron-variant | UBE3C | GRCh38.p7 | 7:157196082 | GAGAACCTCTCCAGG[C/G]TGGTGTCAGAGAGAT | 9690 |
rs12112208 | snp | A/G | 0.0087096 | 0.0654136 | intron-variant | UBE3C | GRCh38.p7 | 7:157184072 | GCTGCGATGCAGGCA[A/G]CCCCGTCGGATCTTC | 9690 |
rs12112338 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157248029 | CTTGGGAGACTAACA[A/G]ACCTGCAGTTCCTGA | 9690 |
rs12112812 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBE3C | GRCh38.p7 | 7:157252701 | GACATCAGTGCCATT[A/G]CCCAGAGGCAGCAGT | 9690 |
rs12112880 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE3C | GRCh38.p7 | 7:157247829 | cagagtGGCATATGC[A/G]GTTAtgaactgggac | 9690 |
rs12530850 | snp | C/T | 0.354665 | 0.227036 | intron-variant | UBE3C | GRCh38.p7 | 7:157247912 | TTTGGAAATAGGGTC[C/T]AATAGCTGCGAGGCC | 9690 |
rs12530989 | snp | A/G | 0.32627 | 0.238082 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138622 | CGCACCCTGCCCCGC[A/G]CCCAACACCTCCCGC | 9690 |
rs12531196 | snp | G/T | 0.222928 | 0.24853 | intron-variant | UBE3C | GRCh38.p7 | 7:157213963 | AAATGTATTATTTGA[G/T]ATAAATAAATATAAA | 9690 |
rs12533082 | snp | A/T | 0.499354 | 0.0179596 | intron-variant | UBE3C | GRCh38.p7 | 7:157221478 | caggcgtggtggctc[A/T]cgcctgtaatcccca | 9690 |
rs12535762 | snp | A/G | 0.356383 | 0.226236 | intron-variant | UBE3C | GRCh38.p7 | 7:157247622 | GCTTGAACCTGGGAG[A/G]CGGAGGTTGCAGTGA | 9690 |
rs12539215 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157180230 | TTATTGCACATTCTG[G/T]GCCATGAAGCTTTTT | 9690 |
rs12540746 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242537 | TTTTTTTTTTTTTTT[A/T]AAATTCCTACTGTCT | 9690 |
rs12669552 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157221494 | cgcctgtaatcccca[A/G]cactttaggaggccg | 9690 |
rs12669987 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | UBE3C | GRCh38.p7 | 7:157239982 | CCACATCTGCATCAC[C/T]GGGGGATCTATTAAA | 9690 |
rs12671829 | snp | A/C | 0.327445 | 0.237702 | intron-variant | UBE3C | GRCh38.p7 | 7:157182993 | ACCTCGTGATCCACC[A/C]GCCTCGGCTTCCCAC | 9690 |
rs12672740 | snp | A/G | 0.444931 | 0.15653 | intron-variant | UBE3C | GRCh38.p7 | 7:157180682 | TATATGATTTGGATC[A/G]TTCTTGATACCCAGA | 9690 |
rs12698033 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157145368 | actaaaaatacaaaa[A/G]ttagccaggcgtggt | 9690 |
rs13221911 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | UBE3C | GRCh38.p7 | 7:157193061 | ATGCTGGAATGCTAG[C/T]GCGCCTGAGTGTCTA | 9690 |
rs13223051 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157155162 | CTTATTTCATGTAGG[A/T]CTGCAAAAAAGAATC | 9690 |
rs13225376 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223917 | aaagccagaacctat[C/T]tcaaaGGGGGGAAGA | 9690 |
rs13226247 | snp | C/T | 0.122758 | 0.215196 | intron-variant | UBE3C | GRCh38.p7 | 7:157248831 | GCGGAGCTCCACTCT[C/T]GAGGCTGCGGCCCAG | 9690 |
rs13229332 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157232947 | tgtacagttcagtgg[G/T]ttttaatatattcac | 9690 |
rs13229333 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157232954 | ttcagtggtttttaa[A/T]atattcactgtgtta | 9690 |
rs13229593 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157154982 | CCCATCTTTGTGATG[A/G]TAAATGGTCAAATAT | 9690 |
rs13231444 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201111 | ggtggatcacttgag[G/T]tcaggagttcaagac | 9690 |
rs13231805 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158063 | TCCTTTTTTTTTttt[A/T]tttttttttcctgta | 9690 |
rs13231807 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158065 | CTTTTTTTTTttttt[A/T]tttttttcctgtaaa | 9690 |
rs13234625 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157213979 | ATAAATAAATATAAA[C/T]ATATTATTTGATGTT | 9690 |
rs13234799 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208184 | ggatcaagcaatcct[C/T]tcacctcagcctcct | 9690 |
rs13235031 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157261304 | agagcaaaactctgt[C/T]tgaaaaaaaaaaaaa | 9690 |
rs13237504 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157220101 | ctgtagtcccagcta[C/T]tcaggaggctgaggt | 9690 |
rs13239285 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | UBE3C | GRCh38.p7 | 7:157202513 | aatacaaaaattagt[C/T]gggcatggtggtgcg | 9690 |
rs13239745 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157233056 | cctatcctgcccttc[C/T]tcccccagccctggc | 9690 |
rs13242040 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | UBE3C | GRCh38.p7 | 7:157199810 | GAAATTTGCTCGAAC[A/G]TTAATGACAGACAGC | 9690 |
rs13245163 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | UBE3C | GRCh38.p7 | 7:157166382 | tgctcacttatatcc[G/T]gaattatttttctga | 9690 |
rs13247303 | snp | A/C | | | intron-variant, utr-variant-5-prime | UBE3C | GRCh38.p7 | 7:157139818 | CTTTTCGAATGCCAC[A/C]TGAAGGGCGTTTTCG | 9690 |
rs13310211 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157166900 | gcatctggtgaaagt[C/T]gctttttccTGTtgg | 9690 |
rs17645539 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157158485 | TAATCACAAAGGCTA[C/G]AGCTGCTAATTGGCC | 9690 |
rs17646047 | snp | A/G | 0.0890129 | 0.19127 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157181660 | TTACAACTCCTGTCC[A/G]GAAGGTGCGAGGTGA | 9690 |
rs17646823 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | UBE3C | GRCh38.p7 | 7:157210898 | TGGATAGAGTCATCT[C/T]TCTTTGTCACTGTAA | 9690 |
rs17646960 | snp | A/G | 0.121022 | 0.21416 | intron-variant | UBE3C | GRCh38.p7 | 7:157214862 | CAAACAGTTAACCAG[A/G]CAGAACTAATAATGA | 9690 |
rs17718923 | snp | C/T | 0.089084 | 0.191327 | intron-variant | UBE3C | GRCh38.p7 | 7:157190732 | CTTTTAGGAAAAAAT[C/T]CACATTCCTTGGATT | 9690 |
rs17719085 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157200505 | CTAGCTGATTACACA[A/G]TTGTGGCTAGAATGT | 9690 |
rs17719499 | snp | A/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157210472 | AACTTACACCTCTGT[A/G]GTTAACTGTGTTTTA | 9690 |
rs17719836 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | UBE3C | GRCh38.p7 | 7:157222944 | GCTGGATCTGGCTGC[A/G]TTCGGGCCTCACCGC | 9690 |
rs17837526 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157157386 | AAAATGATTATTTGT[A/G]GAACAAGATGAAAAG | 9690 |
rs17837719 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157152567 | GTTCTCCTGCAGGGC[A/G]CTTTTCGTTTATGAG | 9690 |
rs17837720 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157152597 | GCTCATTGATCTCGA[C/T]TTCTGATATGTGAGG | 9690 |
rs17837721 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157154906 | TATTTAATAATTACC[C/T]ATTGGAACCCTACCC | 9690 |
rs17837723 | snp | A/C | 0.243633 | 0.249919 | intron-variant | UBE3C | GRCh38.p7 | 7:157198459 | CTCGGAGGCCACAGC[A/C]TGGAAGATCTCCTCT | 9690 |
rs17837724 | snp | G/T | 0.084728 | 0.187577 | intron-variant | UBE3C | GRCh38.p7 | 7:157199449 | AGTCTTTTTCAGAGT[G/T]AATTTTTTTTATTTT | 9690 |
rs17837725 | snp | C/T | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157202175 | CAAACATTAGAACAG[C/T]GTAGAAGTTTTTAAA | 9690 |
rs17837726 | snp | C/T | 0.018544 | 0.0944887 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207530 | TTCCATACATGATAA[C/T]GAATTCTTCGGTGAT | 9690 |
rs17837729 | snp | A/G | 0.3752 | 0.216391 | intron-variant | UBE3C | GRCh38.p7 | 7:157214971 | ACACCATAGAGTCAA[A/G]GGTCAAGGAATAGCT | 9690 |
rs17837732 | snp | A/G | 0.0739243 | 0.177475 | intron-variant | UBE3C | GRCh38.p7 | 7:157231344 | TAAAGTAACCTTCAT[A/G]TAAAAATAGACCTCG | 9690 |
rs17837739 | snp | C/T | 0.416055 | 0.186885 | intron-variant | UBE3C | GRCh38.p7 | 7:157251634 | CAAGTGAAAATAGAC[C/T]TTCTGGAGGAGCAGA | 9690 |
rs28367460 | snp | C/T | 0.359364 | 0.22481 | intron-variant | UBE3C | GRCh38.p7 | 7:157235115 | ATAATGGCTTGAACC[C/T]GGAGGCGGAGGTTGT | 9690 |
rs28400422 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233062 | CTGCCCTTCCTCCCC[A/C]AGCCCTGGCCAACCA | 9690 |
rs28405316 | snp | A/G | 0.163236 | 0.234461 | intron-variant | UBE3C | GRCh38.p7 | 7:157263225 | GCTTCGTGTCCTAAC[A/G]CCACCTTCCCCGGGC | 9690 |
rs28434409 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157142817 | ATTCTTGTAACAAAC[A/G]TGCATAGGTACCCCC | 9690 |
rs28434486 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157200599 | AAGTTCATCTTTTTT[A/T]AATCTAATATTATAG | 9690 |
rs28435188 | snp | A/G | 0.103794 | 0.20279 | intron-variant | UBE3C | GRCh38.p7 | 7:157195575 | TGAACAGGAATGTGT[A/G]TAGCTGTTACTGTAT | 9690 |
rs28446734 | snp | C/T | 0.498945 | 0.022939 | intron-variant | UBE3C | GRCh38.p7 | 7:157204081 | TGGATACTCGAAGTA[C/T]GGTTTCTACTGAATG | 9690 |
rs28446862 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | UBE3C | GRCh38.p7 | 7:157190053 | TGATCTCCCGCCTCA[C/G]CTTTCCAAAGTGCTG | 9690 |
rs28459354 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242526 | GTTGTTTTTTTTTTT[G/T]TTTTTTTTTTTAAAT | 9690 |
rs28459514 | snp | A/G | 0.170733 | 0.237101 | intron-variant | UBE3C | GRCh38.p7 | 7:157196019 | ATTTCAAGACGAGGC[A/G]ATAAGCCCAGATTAT | 9690 |
rs28463479 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE3C | GRCh38.p7 | 7:157227437 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9690 |
rs28464234 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157235210 | AAAAAAAAGAAAAGA[A/G]AAGAAAATCTTTACA | 9690 |
rs28505161 | snp | A/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157226938 | CTAATCTAACTAATC[A/G]TCTAATTGAGAGATG | 9690 |
rs28510264 | snp | A/G | 0.4711 | 0.116682 | intron-variant | UBE3C | GRCh38.p7 | 7:157144202 | ACCGAAGACTGAGGC[A/G]GGAGGATCGCTGGAT | 9690 |
rs28520529 | snp | C/T | 0.143284 | 0.226079 | intron-variant | UBE3C | GRCh38.p7 | 7:157155424 | AAAACCTCACAGTTT[C/T]TTGGGGTTTTTTTTA | 9690 |
rs28523534 | snp | C/T | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157224728 | GAACAAAAGAGTTTC[C/T]TTTGAAGCTGTTCAT | 9690 |
rs28588639 | snp | C/T | 0.154993 | 0.231244 | intron-variant | UBE3C | GRCh38.p7 | 7:157218245 | GAGCTTAGGAGTTTG[C/T]GACCAGCCTGGGCAA | 9690 |
rs28600220 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233069 | TCCTCCCCCAGCCCT[G/T]GCCAACCACTAGTCT | 9690 |
rs28617187 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233068 | TTCCTCCCCCAGCCC[C/T]GGCCAACCACTAGTC | 9690 |
rs28636383 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157145436 | GGCAGGAGAATTGCT[A/T]GAACCCGAGAGGCAG | 9690 |
rs28645654 | snp | A/G | 0.160938 | 0.233598 | intron-variant | UBE3C | GRCh38.p7 | 7:157263241 | CCACCTTCCCCGGGC[A/G]CCTGTCCTAACGCCA | 9690 |
rs28654361 | snp | C/G | 0.150333 | 0.229274 | intron-variant | UBE3C | GRCh38.p7 | 7:157224746 | TGAAGCTGTTCATGT[C/G]CCTTTACTAAACCCT | 9690 |
rs28667423 | snp | A/G | 0.347914 | 0.230028 | intron-variant | UBE3C | GRCh38.p7 | 7:157234476 | GCTTTGCAGTATGGG[A/G]TGTGTGGATTTATTA | 9690 |
rs28714421 | snp | A/G | 0.375399 | 0.216275 | intron-variant | UBE3C | GRCh38.p7 | 7:157204047 | TATTGTACTGAAAGC[A/G]TAAAAACAGAATGGT | 9690 |
rs28720055 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157263733 | CTGTTGGCACCGAAA[A/G]CACTTTTTTTATATT | 9690 |
rs28761283 | snp | A/G | 0.148326 | 0.228391 | intron-variant | UBE3C | GRCh38.p7 | 7:157233461 | TTATTTCATTTTATC[A/G]TAGAGGCAGGGTCTT | 9690 |
rs28837421 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157145347 | ACATGGTGATACTCT[A/G]TCTCTACTAAAAATA | 9690 |
rs28842518 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | UBE3C | GRCh38.p7 | 7:157166530 | CCGATCACCTGAGGT[C/T]GGGAGTTCGAGACCA | 9690 |
rs33910893 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206794 | TCTTGATGGGTGAAA[-/AG]GGCTGCTGAGTAAAG | 9690 |
rs33913991 | in-del | -/A/T/TA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242537 | TTTTTTTTTTTTTTT[-/A/T/TA]AAATTCCTACTGTCT | 9690 |
rs33973695 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157187382 | CGTGTTTTATGGGGT[-/TT]TTTTTTTTTTCTTCT | 9690 |
rs34094179 | snp | A/C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157170179 | ACTGTGAGCAAGGAC[A/C/T]GATAATGGTGTTTTC | 9690 |
rs34110466 | in-del | -/A | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157168335 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs34110923 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196477 | GACAGAATATACATT[-/C]CCTGTATTTCTACAC | 9690 |
rs34137748 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157203283 | GTTAAGTGAGTTATC[-/T]TTGCATCAACAGTGG | 9690 |
rs34169017 | in-del | -/A/AA | 0.0252325 | 0.109451 | intron-variant | UBE3C | GRCh38.p7 | 7:157150378 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAGAG | 9690 |
rs34173241 | in-del | -/G | 0.496937 | 0.0390173 | intron-variant | UBE3C | GRCh38.p7 | 7:157230711 | AAAAAAAAAAAAAAA[-/G]AAACCTCCTAATGTT | 9690 |
rs34246173 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157246911 | TCTCTTTTTTTGAGA[A/C/T]GGAGTTTTTGCTCTT | 9690 |
rs34275282 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157150451 | TACATTTAGAAACGT[-/A]AAAATTTATTCTAGT | 9690 |
rs34300175 | in-del | -/ACAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224775 | TCCCTGCACGTGCGT[-/ACAC]ACACACACACACACA | 9690 |
rs34340717 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157174058 | GGCGTATTTATGACT[A/G]GCTACACTTAAGAGG | 9690 |
rs34341464 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157196882 | CTGAGGCAGGAGAAT[-/G]CTCTTGAACCTGGGA | 9690 |
rs34366505 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157226578 | TTGCCTTTTCCTCTA[-/G]GGGAGCAACTTAATT | 9690 |
rs34371551 | in-del | ATTTA/TTT | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157229930 | TTAATTTATTTATTT[ATTTA/TTT]TTTTTTTTGAGACTG | 9690 |
rs34431702 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186543 | AGTGCAGCTTGATGT[-/A]AAAAAAAAAAGTAGG | 9690 |
rs34498858 | snp | C/T | 0.499996 | 0.00139776 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138643 | CACCTCCCGCGCCCC[C/T]CGCCGCGCTCCCCCA | 9690 |
rs34507522 | in-del | -/G | 0.0517044 | 0.152246 | intron-variant | UBE3C | GRCh38.p7 | 7:157231917 | ATTACCACACTCTTT[-/G]GGGGGGGAGGGAGGC | 9690 |
rs34547256 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227621 | GGAGAATGGCATGAA[-/C]CCCGGGAGGCGGAGG | 9690 |
rs34554349 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157165415 | TTTTTTTTTTTTTTT[-/T]GAGGTGGAGTCTCAC | 9690 |
rs34565014 | in-del | -/A/AA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157257742 | TGAGACCCTGTCTCC[-/A/AA]AAAAAAAAAAAAAAA | 9690 |
rs34624032 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224904 | ATTTTGTCAGAGATA[C/T]TTCTACTAGTGTTAG | 9690 |
rs34722975 | in-del | -/A | 0.138886 | 0.22395 | intron-variant | UBE3C | GRCh38.p7 | 7:157267205 | AGGTGGGCAGATCAC[-/A]AAAGTCAGGAGTTCA | 9690 |
rs34788888 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157178406 | TTCTTACAGTGTTTT[A/G]TAATCTTTAATTTTT | 9690 |
rs34794783 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145974 | TCTCGCGTTGTGTCT[-/A]AAAAGTCATTACCAA | 9690 |
rs34921616 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160584 | TAGTAGTTCATTATG[-/C]CCGTTATGTTTTATT | 9690 |
rs34923864 | in-del | -/AT | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157179108 | TGAACCAAAATTGAC[-/AT]ATGCTTTCATCAGTT | 9690 |
rs34923888 | snp | C/G | 0.133777 | 0.221342 | intron-variant | UBE3C | GRCh38.p7 | 7:157176690 | ATGACTTTTAATGGT[C/G]TGCTTATAGGTAGAG | 9690 |
rs34959154 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224510 | TTTACTTTTTATAAA[-/G]AAAAGAAATGGACAA | 9690 |
rs34981031 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | UBE3C | GRCh38.p7 | 7:157189467 | AAAATAAGAAAGTAG[A/G]CTACCAAAGATAGCC | 9690 |
rs34996036 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157227005 | ATAGTTCTTACATTG[G/T]ATTTTTATTAGCAGA | 9690 |
rs34998574 | in-del | -/T | 0.496937 | 0.0390173 | intron-variant | UBE3C | GRCh38.p7 | 7:157172027 | ATCTTTTTTTTTTTT[-/T]CCTTTTTGAGACGGA | 9690 |
rs35007139 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157247622 | CTTGAACCTGGGAGG[-/A]CGGAGGTTGCAGTGA | 9690 |
rs35045666 | in-del | -/TT | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137566 | CCAGGACTGTATTTC[-/TT]TTTTTTTTTTTTTTT | 9690 |
rs35054342 | in-del | -/A | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157166733 | GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs35129430 | snp | C/T | 0.298398 | 0.245271 | intron-variant | UBE3C | GRCh38.p7 | 7:157160350 | AAAGTACTGGGATTA[C/T]AGGTGTGAGCCCCTG | 9690 |
rs35137829 | snp | A/T | 0.387074 | 0.209071 | intron-variant | UBE3C | GRCh38.p7 | 7:157153702 | TGCAGTCAGTGGCCT[A/T]TTTAAAAAGTTAACT | 9690 |
rs35143652 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157168612 | ATTACTCTTACTTAG[-/C]CCTTAAAAAGGAATG | 9690 |
rs35147293 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213333 | CTATCAGAGTCATCT[-/G]GGGGGAGCAGTTGAA | 9690 |
rs35192251 | snp | A/C | 0.088677 | 0.190984 | intron-variant | UBE3C | GRCh38.p7 | 7:157169022 | TTCTGACCAATTGCT[A/C]CCTCACTCCTCCTTT | 9690 |
rs35216117 | snp | C/G | 0.298144 | 0.245321 | intron-variant | UBE3C | GRCh38.p7 | 7:157156276 | TACTAGAGCCTTTCA[C/G]CTCCACTCCTCACAC | 9690 |
rs35221804 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193661 | CTTCAGAAATTTGTC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs35229326 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231755 | CTGCCTCTGGACCAT[-/G]GGGCTCCTGGCCTTC | 9690 |
rs35241754 | snp | A/G | 0.142272 | 0.225598 | intron-variant | UBE3C | GRCh38.p7 | 7:157175910 | AGCAAATATTTTAGG[A/G]TTTGTGGTCCACATA | 9690 |
rs35273373 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157185433 | AACTTTATACTTTAA[-/T]TTTCCTTTTTTTGTT | 9690 |
rs35298527 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157204398 | GGGAAACTTTGTTTC[-/A]AAAAAAAAAAAAAAA | 9690 |
rs35344384 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157141208 | CATGGGTGCCCTGGC[C/G]TGGTTAAGGAATCTG | 9690 |
rs35366316 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208055 | TTTAATTTGCAAGAC[-/T]TTTTTTTTTTTTTTT | 9690 |
rs35398052 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211425 | TGTTTTTTGACTACT[-/A]AAAGTGGATGCTATA | 9690 |
rs35480997 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157211209 | CCATACTATGAGTGA[-/T]TTTTTTTACTTCCTT | 9690 |
rs35493254 | in-del | -/T | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157155061 | ATTATGTTTTATAAA[-/T]ATGATTTTTAGTGGC | 9690 |
rs35498347 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157178884 | ACTGTGGCTCAGCAT[-/C]CCCGATGGGGAGTGA | 9690 |
rs35507777 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157256933 | TATTCTGCAGACCAT[-/C]CCTGTTATTAAGGTC | 9690 |
rs35549618 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192863 | AAAAGACATGAACTT[-/A]AAAAAAAAAAAAAAG | 9690 |
rs35576161 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157186262 | AACCCTGTCTCTACT[-/A]AAAATACAAAAATTA | 9690 |
rs35592489 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157192393 | CATAAAAACCCTTAC[-/G]GGGGAAGACCATCAC | 9690 |
rs35601959 | in-del | -/AC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264367 | CATGCTCGGCCTGTT[-/AC]ACACACACACCTGGT | 9690 |
rs35610996 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157187107 | CTCCTCTTAAGTTTT[G/T]TCTGCTCTTTTCTGG | 9690 |
rs35612257 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE3C | GRCh38.p7 | 7:157183163 | AACTAGGTATTCTAC[A/G]ATTCAGTTCAATTCT | 9690 |
rs35634293 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268752 | CGAAGACGGGACAGT[-/C]CCCTGGTGCACATCC | 9690 |
rs35659630 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229720 | CAGCCTCAAACTCCT[-/G]GGGCTCAAGTGATCC | 9690 |
rs35681463 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157251861 | TAGAGGGGCTGGGCG[-/C]CAGTGGCTCACGGCT | 9690 |
rs35688726 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268739 | TGCTGCTCTGACTCG[-/A]AAGACGGGACAGTCC | 9690 |
rs35707152 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157229354 | ACTTCTCTCTTGTTG[-/C]CCCAGGCTGGAGTGC | 9690 |
rs35760870 | in-del | -/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160342 | GCCTCCCAAAGTACT[-/G]GGGATTACAGGTGTG | 9690 |
rs35775709 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | UBE3C | GRCh38.p7 | 7:157191348 | CCAGGCTGGAGTGCC[A/G]TGGCGTGATCTCAGC | 9690 |
rs35824397 | snp | C/T | 0.0482946 | 0.147699 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138364 | GTGCTATGTATGAGG[C/T]AAATCTGCGCATGTC | 9690 |
rs35829426 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157207300 | TGCAAATGTTACTTT[-/C]CCCTGATTATATTTG | 9690 |
rs35886673 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157160952 | GCTATCCTTATTTCG[-/T]AACCTTACTGTAATC | 9690 |
rs35887132 | in-del | -/T | 0.0988009 | 0.199095 | intron-variant | UBE3C | GRCh38.p7 | 7:157210285 | AATTGTTTAAAGACC[-/T]TTTTTTTTTTTAAAG | 9690 |
rs35888154 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157145308 | GTATCACCTGGAGTC[-/A]AGAGTTCGAGACCAG | 9690 |
rs35892200 | in-del | -/AA | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157145308 | GTATCACCTGGAGTC[-/AA]GAGTTCGAGACCAGC | 9690 |
rs35967698 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157266544 | CAGAATTCCTCTTGA[-/T]TTTTAGTGGTCACTT | 9690 |
rs35977883 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157213608 | TGAAAGTGAATGTGG[-/A]AAAAAGGAATGTGTT | 9690 |
rs35978696 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | UBE3C | GRCh38.p7 | 7:157198129 | CTCAATTCTCCATCA[A/T]CTAAACTGAAACCAT | 9690 |
rs36004823 | snp | A/G | 0.121717 | 0.214577 | intron-variant | UBE3C | GRCh38.p7 | 7:157263485 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 9690 |
rs36085410 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157182697 | CATACATACATACAT[A/G]CATGAATTATTCATG | 9690 |
rs55674407 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBE3C | GRCh38.p7 | 7:157140951 | GAAATTGAGGAGGAA[A/G]GGCGAGAGGGAAGCT | 9690 |
rs55683148 | snp | A/G | 0.23846 | 0.249734 | intron-variant | UBE3C | GRCh38.p7 | 7:157233519 | TCCTGGCGTCAAGCA[A/G]TCCTCCTGCCTCAAC | 9690 |
rs55705979 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE3C | GRCh38.p7 | 7:157258052 | ACCCAGGCTGAAGCA[A/G]TCTGCCCACCTCAGC | 9690 |
rs55730101 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | UBE3C | GRCh38.p7 | 7:157259817 | TAAAATCATTGGATT[G/T]TACATTTAAAGGGAT | 9690 |
rs55904424 | snp | A/C | 0.154329 | 0.23097 | intron-variant | UBE3C | GRCh38.p7 | 7:157235826 | ACTTCCAAAACATAT[A/C]TGATGACCATCTGAT | 9690 |
rs55961058 | snp | A/G | 0.153997 | 0.230832 | intron-variant | UBE3C | GRCh38.p7 | 7:157240696 | TAATCCGTGAATGGA[A/G]ATTTGAGGGCAAGGG | 9690 |
rs56001915 | snp | C/T | 0.259951 | 0.249802 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137093 | AGGCGCCTGCCACTA[C/T]GCCTGGCTAATTTTT | 9690 |
rs56009768 | snp | C/T | 0.268724 | 0.249298 | intron-variant | UBE3C | GRCh38.p7 | 7:157240401 | TGTGACTCTGATGCA[C/T]GCTGAAATTTGAGAA | 9690 |
rs56058704 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | UBE3C | GRCh38.p7 | 7:157159003 | CGGGGATATTAAGTC[C/T]GTTATCAATAGAGTG | 9690 |
rs56093806 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157147371 | ACTTTCATGTACTAA[C/T]CTTATGTCCTGAAAT | 9690 |
rs56097864 | in-del | -/A | 0.192088 | 0.2432 | intron-variant | UBE3C | GRCh38.p7 | 7:157229927 | TTAATTTATTTATTT[-/A]TTTTTTTTTTTGAGA | 9690 |
rs56147121 | in-del | -/ACAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264419 | GTTACACACACACAC[-/ACAC]CTGGTACTACAGGTG | 9690 |
rs56180280 | in-del | -/A | 0.192088 | 0.2432 | intron-variant | UBE3C | GRCh38.p7 | 7:157229930 | ATTTATTTATTTTTT[-/A]TTTTTTTTGAGACTG | 9690 |
rs56270719 | in-del | -/AA | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157246014 | AAAAAAAAAAAAAAA[-/AA]CAGTGTTCTTCACAA | 9690 |
rs56312341 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157195869 | CAGGGGTGGAGTGGT[A/G]GCGGGGCGGGGGTTG | 9690 |
rs56371005 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | UBE3C | GRCh38.p7 | 7:157182523 | GGAAAAGACTGACAT[A/G]TATATGTGTCTTATG | 9690 |
rs56789772 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157260848 | TAGGTTCTAGACATT[C/T]TGACAGCCAACTAAA | 9690 |
rs56836970 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157264720 | ATTATTACAGGCATG[C/T]ACCACTACAGCCGGC | 9690 |
rs56852731 | in-del | -/T/TTT | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157175158 | TTTTTTTTTTTTTTT[-/T/TTT]GAGGTCATGGACTTC | 9690 |
rs56869231 | in-del | -/TT | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137583 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCTG | 9690 |
rs56922114 | in-del | -/TCTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157224810 | CTCTCTCTCTCTCTC[-/TCTC]CCACTCACTCACTCA | 9690 |
rs56942709 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157235107 | GAGGCAGGATAATGG[A/C]TTGAACCTGGAGGCG | 9690 |
rs56944726 | snp | C/T | 0.259397 | 0.249823 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137091 | ACAGGCGCCTGCCAC[C/T]ATGCCTGGCTAATTT | 9690 |
rs57114090 | in-del | -/AAAAAAAAAAAAAAAAAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157261321 | GAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAA]TCCCAAATAGACTAA | 9690 |
rs57210743 | snp | C/T | 0.26518 | 0.249539 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137085 | GGGACTACAGGCGCC[C/T]GCCACTATGCCTGGC | 9690 |
rs57309314 | in-del | -/G | 0.499816 | 0.0095829 | intron-variant | UBE3C | GRCh38.p7 | 7:157146411 | TACTCTAGTACAGAC[-/G]GGGGTTTCACCATGT | 9690 |
rs57487459 | snp | A/C | 0.222928 | 0.24853 | intron-variant | UBE3C | GRCh38.p7 | 7:157162348 | TACTGGTATGTGCCA[A/C]CATGCCCGGCTAATT | 9690 |
rs57511186 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157250648 | TTTATTTGGTTACAA[C/T]TTATTTAGTTGCTTT | 9690 |
rs57543956 | in-del | -/AC | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264423 | CACACACACACACAC[-/AC]CTGGTACTACAGGTG | 9690 |
rs57553468 | snp | A/C | 0.0422008 | 0.138995 | intron-variant | UBE3C | GRCh38.p7 | 7:157230254 | ACCAGTAATTTTCCC[A/C]CCTTTTCAGCCAAAT | 9690 |
rs57600759 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | UBE3C | GRCh38.p7 | 7:157145767 | AATTAATAAGCTTTT[A/T]TTTTAGAGTGGTTTA | 9690 |
rs57603221 | snp | A/G | 0.148326 | 0.228391 | intron-variant | UBE3C | GRCh38.p7 | 7:157165917 | GATGGGGTTTCCTTT[A/G]TAGGTGACTAGCTGC | 9690 |
rs57763939 | in-del | -/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157233725 | TTGGACATAGGTTTT[-/TT]GTTTTTCTTGGGCAT | 9690 |
rs58070039 | in-del | -/ACAC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264475 | GTTACACACACACAC[-/ACAC]CTGGTACTACAGGTG | 9690 |
rs58093796 | in-del | -/GA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158005 | AGAGAGAGAGAGAGA[-/GA]TACATATAAACATGG | 9690 |
rs58138213 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148749 | TTTTTTTTTTTTTTT[-/T]CCTTTAAGAGACAGG | 9690 |
rs58300955 | snp | C/G | 0.48435 | 0.0870631 | intron-variant | UBE3C | GRCh38.p7 | 7:157234681 | AGAAAGGGCTCCAAC[C/G]TGACTTCACTACCGT | 9690 |
rs58313408 | snp | A/C | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157238846 | GTTCAGGAGATGAAG[A/C]TGGAAAGGAAGGGAG | 9690 |
rs58383368 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157169577 | GTCGGTGTTTTGCCA[C/T]GTTGACCAGGCTGGT | 9690 |
rs58409418 | snp | A/T | 0.170408 | 0.236992 | intron-variant | UBE3C | GRCh38.p7 | 7:157185515 | AACTAAAGACCCCAT[A/T]TTGAGCCAGGCACTC | 9690 |
rs58522767 | snp | C/T | 0.0834505 | 0.186444 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186968 | CTTCACCACCATGGC[C/T]TCCGTCTGCCACACG | 9690 |
rs58545906 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE3C | GRCh38.p7 | 7:157142797 | ACCTCCGCGTCCTGC[A/G]GTATATTCTTGTAAC | 9690 |
rs58654062 | snp | A/G | 0.153 | 0.230415 | intron-variant | UBE3C | GRCh38.p7 | 7:157241601 | CAGTCCTCATGCATT[A/G]CCAATGGGAAGATAA | 9690 |
rs58776863 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267834 | AGACCCACGAGGATA[C/T]TCACACTGCACGCCT | 9690 |
rs58826821 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | UBE3C | GRCh38.p7 | 7:157220285 | ATAACTTGAGAAAAT[A/G]TACTGTGTCTGTTTT | 9690 |
rs58895943 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157177945 | TTTTTTTTTTTTTTT[A/T]AGAAAAAGGAAAAAC | 9690 |
rs58897972 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264485 | CACACACACCTGGTA[C/T]TACAGGTGTGCGCCA | 9690 |
rs58975924 | in-del | -/CAG | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157193290 | AAAGAAAAATTTCAG[-/CAG]AAGAACAAATTATTG | 9690 |
rs58983636 | snp | A/T | 0.331874 | 0.236213 | intron-variant | UBE3C | GRCh38.p7 | 7:157162411 | TGTTGGCCAGGCTGG[A/T]CTCGAACTCCTGACC | 9690 |
rs59014357 | in-del | -/GTT | 0.514585 | 0.064862 | intron-variant | UBE3C | GRCh38.p7 | 7:157166941 | GTGGTGGTGGTGGTT[-/GTT]TTTGAGACAAAGTCT | 9690 |
rs59115545 | snp | C/T | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157166147 | TATTTTATTGCTTTA[C/T]GTTATCCCAAATGTC | 9690 |
rs59140781 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157256540 | GGCGGGGGGAGGCAG[A/G]GAATTCCGCTTTTGC | 9690 |
rs59143683 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157161655 | GATAGGGTTTCACCA[C/T]GTAGCCCAGGCTGGT | 9690 |
rs59176594 | snp | G/T | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157193417 | GGATGCCATGCTGTG[G/T]TGGCCTTGACTCCTT | 9690 |
rs59177688 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157153520 | AGGCTGGTCTTGAAC[C/T]GAGCTCAATTGATCC | 9690 |
rs59178327 | snp | C/T | 0.499937 | 0.0055907 | intron-variant | UBE3C | GRCh38.p7 | 7:157139411 | GGCTGGGACTCGGGG[C/T]TGGACTCGGGGCTGG | 9690 |
rs59204525 | in-del | -/ATT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157254405 | TTAATTTATTTATTT[-/ATT]TTTTTTTTTCAGACT | 9690 |
rs59205261 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | UBE3C | GRCh38.p7 | 7:157229572 | CCCACCTGCCTTGGC[C/G]TCCCAAAGTGCTGGG | 9690 |
rs59247346 | snp | C/T | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157183383 | GGAAGTCGAGGTGTG[C/T]GGGAATGGGGAGCTT | 9690 |
rs59540123 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157230409 | GAAAAAAAAAAAAAA[-/A]TTACAGGCCGGGCAC | 9690 |
rs59571492 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | UBE3C | GRCh38.p7 | 7:157234990 | TGAGGTCGGGAGCTC[A/G]AGACCAGCCTGACCA | 9690 |
rs59577520 | in-del | -/G | 0.331874 | 0.236213 | intron-variant | UBE3C | GRCh38.p7 | 7:157153995 | AGCGAGGCCCTGTCT[-/G]GGGGGGGGAAAAGTT | 9690 |
rs59580574 | snp | A/G | 0.154661 | 0.231107 | intron-variant | UBE3C | GRCh38.p7 | 7:157239303 | ATGGTATGAGTGAAC[A/G]GCACAGACCTAACAT | 9690 |
rs59596464 | snp | C/T | 0.127966 | 0.219365 | intron-variant | UBE3C | GRCh38.p7 | 7:157202148 | AGATTTGAAGTAAAT[C/T]AAAGACTGCTGCAAA | 9690 |
rs59637158 | in-del | -/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137584 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCTG | 9690 |
rs59797848 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | UBE3C | GRCh38.p7 | 7:157192288 | CCACGTTTTTAAAGT[A/T]TTCTTTTAAGCTTGT | 9690 |
rs59802408 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157204127 | CATCTTGAAGTTGCA[A/G]AATCCTAAACTGAAC | 9690 |
rs59869013 | in-del | -/T | 0.257732 | 0.24988 | intron-variant | UBE3C | GRCh38.p7 | 7:157200311 | AAAATAAGAATGGAG[-/T]TTAGTTGTTGTTTAT | 9690 |
rs59950796 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157153606 | CACGCCCAGCCAGAA[A/G]GTCATAATTCTTGAT | 9690 |
rs60071570 | in-del | -/AG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157206795 | CTTGATGGGTGAAAG[-/AG]GCTGCTGAGTAAAGA | 9690 |
rs60098600 | in-del | -/GA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157237896 | ACCACTAAAAAAAAA[-/GA]AAAAAAGTAGCCAGG | 9690 |
rs60161618 | in-del | -/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157189758 | GGTTCTTTTTTCTCC[-/C]TCTTTCTCACTCTTT | 9690 |
rs60166169 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264442 | GGTACTACAGGTGTG[A/C]GCCAACATGCTCGGC | 9690 |
rs60229102 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | UBE3C | GRCh38.p7 | 7:157210167 | GGGCGGTAGGGTGAC[A/T]CTCTCTCCAAAAAAA | 9690 |
rs60257662 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158072 | TTTTTTTTTTTTTTT[-/T]CCTGTAAAGGGAGCC | 9690 |
rs60283573 | snp | C/T | 0.375399 | 0.216275 | intron-variant | UBE3C | GRCh38.p7 | 7:157215455 | ATATCCAGTATAGAT[C/T]AGATATATTATAAAT | 9690 |
rs60291484 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157219917 | AAAAAAAAAAAAAAA[-/A]TTGCAAGGGCCAGCC | 9690 |
rs60292847 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | UBE3C | GRCh38.p7 | 7:157239429 | CAGGATCCTGATGCT[C/T]CTGGGAGGGTAACAC | 9690 |
rs60373906 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157264428 | ACACACACACACCTG[C/G]TACTACAGGTGTGAG | 9690 |
rs60465114 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157219693 | GATCACCTGAGGTCA[A/G]TTCGAGACCACCCTG | 9690 |
rs60479472 | in-del | -/CAAA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157153842 | AAACAAACAAACAAA[-/CAAA]AAAACGGGCATGGTG | 9690 |
rs60535165 | snp | A/G | 0.121717 | 0.214577 | intron-variant | UBE3C | GRCh38.p7 | 7:157247980 | GTTCATGTGGTTTTC[A/G]GTCTCGCAGTGTGTG | 9690 |
rs60648842 | snp | A/G | 0.295854 | 0.245759 | intron-variant | UBE3C | GRCh38.p7 | 7:157236832 | CACCTCCCGGGTTCA[A/G]GCGATTCTCCTGCCT | 9690 |
rs60681769 | in-del | -/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193677 | TTTTTTTTTTTTTTT[-/T]GGTGAAAACATTCTT | 9690 |
rs60687230 | snp | A/T | 0.26326 | 0.249648 | intron-variant | UBE3C | GRCh38.p7 | 7:157200230 | TCACATGCTCTTTCA[A/T]GCTTTTACTGTTTTT | 9690 |
rs60804162 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE3C | GRCh38.p7 | 7:157258476 | CTTTGTTTTTGAGAC[A/G]GAGTTTTACTCTGTC | 9690 |
rs60831703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157231754 | GGCTGCCTCTGGACC[A/G]TGGGCTCCTGGCCTT | 9690 |
rs60860214 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157235967 | AAACTGTATATTGAT[G/T]GATTGTGATATTTAT | 9690 |
rs61030882 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | UBE3C | GRCh38.p7 | 7:157194089 | GCCCTTTGATTTACA[A/G]TGTTCAGTTCTTTTA | 9690 |
rs61061933 | in-del | -/T/TT | 0.375 | 0.216506 | intron-variant | UBE3C | GRCh38.p7 | 7:157156325 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCCTGC | 9690 |
rs61335016 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157255760 | ACAATATACAGCAAT[A/T]ATTTTAGGTTTAGGG | 9690 |
rs61476132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157192350 | CGATCCGCCATCTGC[A/G]GTGGAGCCGCCACCA | 9690 |
rs61545466 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | UBE3C | GRCh38.p7 | 7:157154004 | CCTGTCTGGGGGGGG[A/G]AAAGTTAACTTTTTC | 9690 |
rs61590554 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157244078 | TCTACTAAAAATACA[A/C]AAATTTGCTGGGCAT | 9690 |
rs62001020 | snp | A/G | 0.0338882 | 0.125681 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186933 | AACCTGGTGTGGAGG[A/G]ACTCTGCGAGCGAGG | 9690 |
rs62001021 | snp | A/G | 0.00212491 | 0.032526 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157186861 | CTGTCAGTATCATAC[A/G]TAACAGAGGAATGCC | 9690 |
rs62001022 | snp | G/T | 0.42344 | 0.180051 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207399 | TTCTTTAATTCAAGG[G/T]CTATGGTACCGTTGC | 9690 |
rs62001023 | snp | A/G | 0.00206177 | 0.0320411 | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157207549 | TTCTTCGGTGATCCC[A/G]TAGAAGGTAAGGATT | 9690 |
rs62001024 | snp | A/G | 0.000411851 | 0.0143442 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223270 | GGGTTTGGAGTCCCC[A/G]CCGCTGTCTGTGTCT | 9690 |
rs62491931 | snp | A/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157226282 | TCCAATGACACTGCC[A/G]TTAGTAAAGGAGAAT | 9690 |
rs62491932 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | UBE3C | GRCh38.p7 | 7:157228580 | TCCTGAAGCAGAGGA[A/C]ATTTATTCCAGAAGC | 9690 |
rs62491933 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157230411 | AAAAAAAAAAAAAAT[A/T]ACAGGCCGGGCACGG | 9690 |
rs62491935 | snp | A/G | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157140314 | GGAGGAACTGCTGTT[A/G]TTAAGATTGTGCTGT | 9690 |
rs62491936 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE3C | GRCh38.p7 | 7:157141425 | TGTTGTGGGACCGTC[C/G/T]TAGAGTGCACTTAAC | 9690 |
rs62491937 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157146011 | GGTAACCTAGATTTT[C/T]TCGTATTTTCTAGTA | 9690 |
rs62491940 | snp | A/G | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157157748 | GGGAGGCCAAGGTGG[A/G]TGGATCACCTGAGGT | 9690 |
rs62491942 | snp | C/T | 0.142609 | 0.225759 | intron-variant | UBE3C | GRCh38.p7 | 7:157160302 | CTGGTCTCGAACTCC[C/T]GACCTCAGGCGATCT | 9690 |
rs62491943 | snp | C/T | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157160317 | TGACCTCAGGCGATC[C/T]GCCGGCCTTGGCCTC | 9690 |
rs62491945 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | UBE3C | GRCh38.p7 | 7:157162886 | CTAAAGACTGGAACA[A/G]TCTTTGGGGGAGAAG | 9690 |
rs62491946 | snp | G/T | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157167615 | CGATCTCGGCTCACT[G/T]CAAGCTCCACCTCCC | 9690 |
rs62491947 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | UBE3C | GRCh38.p7 | 7:157168119 | CATTTTGGGAGGCCA[A/G]GGCTGGAGGATCATG | 9690 |
rs62491949 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157169391 | TTTTTTTTTTTTTAA[A/T]TTGAGACTGAGTCTC | 9690 |
rs62491950 | snp | A/G | 0.142947 | 0.22592 | intron-variant | UBE3C | GRCh38.p7 | 7:157171230 | TCCCGGGCTCAAGCA[A/G]TCGGTGGTGTCTCAG | 9690 |
rs62491951 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157176574 | GCCACCGTGCCCAGC[C/T]AAACCCATGTTTCTT | 9690 |
rs62493372 | snp | C/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157240618 | AATAAAGGGTGAATT[C/G]GTTGCAAGTTCAGAG | 9690 |
rs62493373 | snp | C/T | 0.148326 | 0.228391 | intron-variant | UBE3C | GRCh38.p7 | 7:157240646 | GAGTGGTTACAAGAG[C/T]CTGCCTTTGAATCTA | 9690 |
rs62493374 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242540 | TTTTTTTTTTTTTAA[A/T]TTCCTACTGTCTTTC | 9690 |
rs62493375 | snp | C/T | 0.196771 | 0.244268 | intron-variant | UBE3C | GRCh38.p7 | 7:157247648 | AGTGAGCTGAGATCG[C/T]GCGGCTGCACTCCAG | 9690 |
rs62493376 | snp | A/G | 0.15698 | 0.23205 | intron-variant | UBE3C | GRCh38.p7 | 7:157248972 | GCTCCAGCACTGTCT[A/G]GGGGGTGTGTTCATT | 9690 |
rs62493377 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | UBE3C | GRCh38.p7 | 7:157258087 | CAAGTAGCTGTGACT[A/G]CAGGCATGTACCACC | 9690 |
rs62493378 | snp | C/G | 0.164219 | 0.234823 | intron-variant | UBE3C | GRCh38.p7 | 7:157263275 | TCCCAGGCACCTGTC[C/G]TAACGCCACCTTCCC | 9690 |
rs62493379 | snp | A/G | 0.151334 | 0.229706 | intron-variant | UBE3C | GRCh38.p7 | 7:157266246 | GTGAACCCGGGAGGC[A/G]GATGTTGCAGTAAGC | 9690 |
rs62493391 | snp | A/T | 0.170733 | 0.237101 | intron-variant | UBE3C | GRCh38.p7 | 7:157196184 | CGGATGTTCTCTAGA[A/T]GGTGGAATGACAAGG | 9690 |
rs62493392 | snp | G/T | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157196449 | GCTGGTAGTTCTTTA[G/T]ATCTAGTCTGTCCGA | 9690 |
rs62493393 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157196514 | TGTTCTGGAGAAGAC[A/G]TTCTAGGTTGAGCAC | 9690 |
rs62493394 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157197314 | TTTTCTGCAAACAAA[A/G]CATTAACACTAAGTA | 9690 |
rs62493395 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157197526 | TTTTTTTTTTTTTTA[A/T]TGCTGGAGGTATTGT | 9690 |
rs62493396 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157206281 | TATTTATTTTTTTTG[G/T]AAACGGAGTCTCGCC | 9690 |
rs62493426 | snp | A/G | 0.147656 | 0.228091 | intron-variant | UBE3C | GRCh38.p7 | 7:157215322 | CTGGTATCCCTGCAT[A/G]CCTTGGATTTGCATT | 9690 |
rs62493428 | snp | A/G | 0.148661 | 0.22854 | intron-variant | UBE3C | GRCh38.p7 | 7:157215648 | TCTGTGGTGATTTCC[A/G]TTGTCTTTAATTAGA | 9690 |
rs62493429 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | UBE3C | GRCh38.p7 | 7:157217697 | CAAAAATCAGCCGGG[C/T]GTGGTGGCAGACGCC | 9690 |
rs66662472 | in-del | -/T | 0.0894459 | 0.191631 | intron-variant | UBE3C | GRCh38.p7 | 7:157199384 | ATAATAGATACCCTA[-/T]CCTGAGATATTTAAA | 9690 |
rs66853524 | in-del | -/CT | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157189828 | GTTTGTGACGGAGTC[-/CT]TTGCCTTGTCGCCCA | 9690 |
rs67100354 | in-del | -/CAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157193288 | AAAAAGAAAAATTTC[-/CAG]AGAAGAACAAATTAT | 9690 |
rs67204083 | in-del | -/CTTC | | | intron-variant | UBE3C | GRCh38.p7 | 7:157234127 | TTTGCAAGTATTTTC[-/CTTC]TTCTCTGGATTGTCT | 9690 |
rs67286782 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | UBE3C | GRCh38.p7 | 7:157162756 | CTCCTGTGCTCAAGT[C/G]ATTCTCCTGCCTTGG | 9690 |
rs67483339 | in-del | -/AT | 0.495818 | 0.0455352 | intron-variant | UBE3C | GRCh38.p7 | 7:157157974 | AACAGATATATATAG[-/AT]ATATATATATATAGA | 9690 |
rs71189984 | in-del | -/TT | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157150390 | TATCTTGTTAGACTC[-/TT]TTTTTTTTTTTTGAG | 9690 |
rs71189985 | in-del | -/A | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157162205 | TCCGTCTCAAAAAAG[-/A]AAAAAAAAATTAAAT | 9690 |
rs71189987 | in-del | -/A | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157198543 | CCTGTCGAAAAAAAT[-/A]AAAAAAAAAAAGACA | 9690 |
rs71189988 | in-del | -/T | 0.0894459 | 0.191631 | intron-variant | UBE3C | GRCh38.p7 | 7:157199382 | TAATAGATACCCTAC[-/T]CTGAGATATTTAAAA | 9690 |
rs71189989 | in-del | -/A | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157217334 | GCAAGATTCCGTCTC[-/A]AAAAAAAAAAAATCA | 9690 |
rs71189990 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157257763 | ACGTTCCTGAGGCAA[-/T]TTTTTTTTTTTTTTT | 9690 |
rs71189991 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157261339 | TTAGTCTATTTGGGA[-/T]TTTTTTTTTTTTTTT | 9690 |
rs71189993 | in-del | -/GT | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264317 | CACCTGTAATACCAG[-/GT]GTGTGTGTGTGTGTG | 9690 |
rs71303921 | in-del | -/A | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157210290 | GAACAGAAATCCTTT[-/A]AAAAAAAAAAAGGTC | 9690 |
rs71303922 | in-del | -/T | 0.125874 | 0.217008 | intron-variant | UBE3C | GRCh38.p7 | 7:157196755 | TCTCAAACTCCCGAC[-/T]CTCAGGTGATCCACC | 9690 |
rs71303923 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157192877 | TTTGATAATCCCTTC[-/T]TTTTTTTTTTTTTTA | 9690 |
rs71303924 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157148108 | CTCTGTCTCAAAAAA[-/A]ACAAAATAAAACAAA | 9690 |
rs71516463 | multinucleotide-polymorphism | AT/GA | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157167727 | ATTTTTAGAAGAGGT[AT/GA]GGTTTCACCATTTTA | 9690 |
rs71522068 | in-del | -/CTGGACTCGGGG | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157139434 | GGGCTGGACTCGGGG[-/CTGGACTCGGGG]CCGAGACTTGGGGCT | 9690 |
rs71522069 | in-del | -/A | 0.0524604 | 0.153226 | intron-variant | UBE3C | GRCh38.p7 | 7:157147065 | TATTCACAAAAAAAA[-/A]CCTGTGGAATTTTGA | 9690 |
rs71522070 | in-del | -/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157153568 | AGGTAATCCCAAGTG[-/G]TTGGGATTACAGGTG | 9690 |
rs71522075 | in-del | -/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157200694 | GGCTGGAGTGTAGTG[-/G]TGCAATCTTGGCTCA | 9690 |
rs71522076 | in-del | -/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157208056 | TTAATTTGCAAGACT[-/T]TTTTTTTTTTTTTTT | 9690 |
rs71522077 | in-del | -/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157237919 | AGCCAGGCATGGTGG[-/G]TGTGTGTCTGTAGTC | 9690 |
rs71522078 | in-del | -/GTT/GTTGTT/TT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157242510 | TGAGACTGAGCCTGA[-/GTT/GTTGTT/TT]GTTGTTTTTTTTTTT | 9690 |
rs71522079 | in-del | -/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157251862 | AGAGGGGCTGGGCGC[-/C]AGTGGCTCACGGCTG | 9690 |
rs71527759 | multinucleotide-polymorphism | ATAGTGGCA/GTGGTGGCG | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137085 | AAAAATTAGCCAGGC[ATAGTGGCA/GTGGTGGCG]GGCGCCTGTAGTCCC | 9690 |
rs71538010 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157200015 | CCCACTTTGTCATGG[C/T]GTGTGACTGATAAAC | 9690 |
rs71538011 | snp | A/G | 0.122064 | 0.214785 | intron-variant | UBE3C | GRCh38.p7 | 7:157262058 | GCTTTTCATTTATCC[A/G]GTGACTTTGCCAGCA | 9690 |
rs71723392 | in-del | -/ACG | 0.143622 | 0.226238 | intron-variant | UBE3C | GRCh38.p7 | 7:157142366 | TGTATAGATCTGTGT[-/ACG]ACAAGTCTGACTTGA | 9690 |
rs71895057 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157201659 | TTTTTTTTTTTTTTT[-/A]AGAAATGTTTTGAAT | 9690 |
rs73174376 | snp | A/G | 0.329084 | 0.237162 | intron-variant | UBE3C | GRCh38.p7 | 7:157158104 | TGTTTCATGGCCCAG[A/G]CTGGTCTCAAACTCT | 9690 |
rs73174402 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE3C | GRCh38.p7 | 7:157199873 | TAACTTGTATTATTA[C/T]CATTTTTTCGTTTTT | 9690 |
rs73176416 | snp | A/G | 0.332106 | 0.236133 | intron-variant | UBE3C | GRCh38.p7 | 7:157222210 | AATTTTGAGAGTTAT[A/G]AAGCTATTCTGGATA | 9690 |
rs73176422 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157232156 | TTGCCTTATTTTTTT[A/T]AATAAGGACACCTGT | 9690 |
rs73176423 | snp | C/T | 0.356169 | 0.226336 | intron-variant | UBE3C | GRCh38.p7 | 7:157232956 | CAGTGGTTTTTAATA[C/T]ATTCACTGTGTTATG | 9690 |
rs73176427 | snp | C/T | 0.375598 | 0.21616 | intron-variant | UBE3C | GRCh38.p7 | 7:157235184 | ACAAGAGCAAAACTC[C/T]GTCTCAAATTAAAAA | 9690 |
rs73176433 | snp | A/G | 0.35574 | 0.226537 | intron-variant | UBE3C | GRCh38.p7 | 7:157238798 | GGCTCTCCAAGGTTT[A/G]GAGTCCAGAGAGTAG | 9690 |
rs73176441 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157246436 | CTAATATTTACAGTG[C/T]ATGATATGGTTGGGT | 9690 |
rs73176446 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157258769 | CCGGCCCCCCAAGTA[C/T]TTTTTTATATTTCTG | 9690 |
rs73492566 | snp | A/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157166467 | TTTTGAGGGCTGGGC[A/G]CGATGGCTCACGCCT | 9690 |
rs73492569 | snp | C/G | 0.147991 | 0.228242 | intron-variant | UBE3C | GRCh38.p7 | 7:157167283 | CTACATCTACATGAC[C/G]TGATGGTGTTCTTGA | 9690 |
rs73492570 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3C | GRCh38.p7 | 7:157172358 | ATATAATTTATTTTT[A/G]GAAATTTTTGTTTAT | 9690 |
rs73492583 | snp | A/G | 0.0661888 | 0.16945 | intron-variant | UBE3C | GRCh38.p7 | 7:157178859 | AATGGTAAGTAGTAG[A/G]CAGGATCAGAACTGT | 9690 |
rs73492613 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE3C | GRCh38.p7 | 7:157265968 | CACTTTTCATCATGC[A/G]TTTGGTCTATAGATG | 9690 |
rs73505598 | snp | A/G | 0.12932 | 0.218944 | intron-variant | UBE3C | GRCh38.p7 | 7:157198978 | ATTTCAGAAATATGT[A/G]TACATTCACATGGAA | 9690 |
rs73507518 | snp | A/G | 0.148661 | 0.22854 | intron-variant | UBE3C | GRCh38.p7 | 7:157215512 | AGTATATATTATACA[A/G]TTTATAACTATAATA | 9690 |
rs73507531 | snp | G/T | 0.126219 | 0.217206 | intron-variant | UBE3C | GRCh38.p7 | 7:157224020 | GAAACGATGTTTTTT[G/T]TTTTCTGAGACAGGA | 9690 |
rs73507540 | snp | A/G | 0.238749 | 0.249747 | intron-variant | UBE3C | GRCh38.p7 | 7:157232377 | TTGTTTGTTTGAGAC[A/G]GAGTCTCTCCTTGCT | 9690 |
rs73507561 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | UBE3C | GRCh38.p7 | 7:157237522 | TTAAGTAGGTCTTGC[C/T]TACTATTGAGTTATT | 9690 |
rs73509646 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | UBE3C | GRCh38.p7 | 7:157242758 | AACTAGAAGTCGAGG[A/G]AAAAAAGGAAGGGTC | 9690 |
rs73509649 | snp | C/T | 0.118584 | 0.212673 | intron-variant | UBE3C | GRCh38.p7 | 7:157243461 | CTCTGCTCAGTTATC[C/T]GTGGTAGACATCTGC | 9690 |
rs73509658 | snp | C/T | 0.203882 | 0.245709 | intron-variant | UBE3C | GRCh38.p7 | 7:157250864 | TGTTGTGGTGACCTG[C/T]CTGAGGCCTTTGCTA | 9690 |
rs73509667 | snp | A/G | 0.20511 | 0.245937 | intron-variant | UBE3C | GRCh38.p7 | 7:157259681 | TCCTTTGAAAGGCAC[A/G]TTTAGAGACACAGAG | 9690 |
rs73743203 | snp | A/C | 0.0325976 | 0.123435 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138151 | AACTTAAAATGGCTC[A/C]ACTTACAATTTTTTG | 9690 |
rs73743204 | snp | C/G/T | 0.0182019 | 0.0936463 | intron-variant | UBE3C | GRCh38.p7 | 7:157139733 | CCAAGGTGAACTTAC[C/G/T]CTTTCTGGGTGTTTC | 9690 |
rs73743205 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157141494 | TGCTTGGTACAGCCC[A/G]TTGCCCCTATGCTAC | 9690 |
rs73743208 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157149948 | TTACCATTTGTCAGC[A/C]TGAAGGAGAAGCCAT | 9690 |
rs73743209 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157150492 | GCATAAGAGAAGATG[C/T]ATGGGAAAGGTGATT | 9690 |
rs73743210 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157150766 | TTATCTGAACAGTAA[A/G]GATAGCTAGTTTCCC | 9690 |
rs73743211 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157151703 | AATTCACTGATTTAG[A/T]TCATTTAGCTTTTTA | 9690 |
rs73743214 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | UBE3C | GRCh38.p7 | 7:157172587 | GACTTTCTGTAAACC[A/G]AGAACGTGCAGAGAA | 9690 |
rs73743215 | snp | A/G/T | 0.0512794 | 0.153279 | intron-variant | UBE3C | GRCh38.p7 | 7:157173446 | TGCCCCAGTCTTCAC[A/G/T]TTGTTTGCCTTCTAC | 9690 |
rs73743216 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157176998 | GAACCACCTGCAGCT[A/C]CTTTTATGACTAATC | 9690 |
rs73743306 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157236607 | TCCTTTTGTAAAATG[C/T]TCACTGAATTTGCTG | 9690 |
rs73743308 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | UBE3C | GRCh38.p7 | 7:157238349 | TGTAAGTAGCTAGCA[C/T]TGGTCAAGCACTCAA | 9690 |
rs73743311 | snp | G/T | 0.154661 | 0.231107 | intron-variant | UBE3C | GRCh38.p7 | 7:157238579 | ACTAAGCTGGGAAAG[G/T]TGCGGGCAGGAGCAG | 9690 |
rs73743324 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157244583 | ATAGAGATGCATTTG[A/T]AAAGCATTATTTTTT | 9690 |
rs73743325 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157245580 | CATTTTATTCATTCT[C/T]TCATTAAGAAACCCT | 9690 |
rs73743327 | snp | C/T | 0.00324127 | 0.0401264 | intron-variant | UBE3C | GRCh38.p7 | 7:157248335 | GAAGGCTTGTATATT[C/T]GATGCTAACGTTGTC | 9690 |
rs73743332 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | UBE3C | GRCh38.p7 | 7:157253068 | AAATACTTTTTAAAA[A/T]TTTTTTTATTTAAAA | 9690 |
rs73743335 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | UBE3C | GRCh38.p7 | 7:157256553 | AGAGAATTCCGCTTT[A/T]GCATTTACAATCGGT | 9690 |
rs73743399 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157259361 | CAAGGGGTGCAGGCA[A/G]GTTATCTTGAGAATG | 9690 |
rs73743400 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157260315 | CAGGGCCAGGAAAAC[A/G]CTGCCGCCTACAAGC | 9690 |
rs73743402 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | UBE3C | GRCh38.p7 | 7:157263174 | TTCTAGCCTTTTCCC[A/G]GAAAATCAGCTTAGT | 9690 |
rs73746704 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157209321 | TGATTGCACTGAATA[C/T]AGTCCTAATGCATCG | 9690 |
rs73746706 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157213414 | GCACGCCTGTGGTGG[A/G]CTTGTCTTAGTGCTC | 9690 |
rs73746708 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157224796 | CACACACACACACTC[A/T]CTCTCTCTCTCTCTC | 9690 |
rs74354973 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157226331 | GGAGCTCACTGGCAC[A/G]TTTCGTCGTATGTTC | 9690 |
rs74456023 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157167541 | CCTCTCTCTCTCTCT[C/T]TTCTTTTTTTTTTTG | 9690 |
rs74472351 | in-del | -/AT | 0.181022 | 0.240296 | intron-variant | UBE3C | GRCh38.p7 | 7:157261476 | TCAATGTTCTAACAT[-/AT]GTGAAATTTAATTGA | 9690 |
rs74496244 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | UBE3C | GRCh38.p7 | 7:157172430 | GTGAAAAATAAGTCT[G/T]CCTCGCTACAAACCA | 9690 |
rs74582336 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157201661 | TTTTTTTTTTTTTAA[G/T]AAATGTTTTGAATAA | 9690 |
rs74592041 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157170993 | CTAATTTTTTTTTTT[G/T]TAGAGATGAGGTCTT | 9690 |
rs74600078 | in-del | -/T | 0.498908 | 0.0233371 | intron-variant | UBE3C | GRCh38.p7 | 7:157197510 | AATAAAAATAATTTG[-/T]TTTTTTTTTTTTTTA | 9690 |
rs74605387 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157253311 | TGTGTTGCTTTTCTC[A/G]TGAGCACTCTTGTGG | 9690 |
rs74629950 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157147683 | GTTTGGTGGGTTTTT[G/T]GGTAGATATTCTTTA | 9690 |
rs74659965 | in-del | -/TTGT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157248315 | CATATGGCTCTTTGT[-/TTGT]AGAAGGCTTGTATAT | 9690 |
rs74671488 | snp | A/G/T | 0.0379877 | 0.132479 | intron-variant | UBE3C | GRCh38.p7 | 7:157152241 | GGGAGAGAGCTGGGG[A/G/T]AAAGGTAATTAGGGA | 9690 |
rs74732565 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137581 | TTTTTTTTTTTTTTT[G/T]TTTGAGACGGAGTCT | 9690 |
rs74859047 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157144412 | GTCTGTTTTGGGAGA[C/T]GGGGGAAACTTAAGT | 9690 |
rs74920287 | snp | C/T | 0.147321 | 0.227941 | intron-variant | UBE3C | GRCh38.p7 | 7:157149060 | TAAGGTTAAGAATTC[C/T]TTTTTTGTTTTTTGA | 9690 |
rs74958275 | snp | A/G | 0.143622 | 0.226238 | intron-variant | UBE3C | GRCh38.p7 | 7:157153922 | GGCTTGGTGGGGCGG[A/G]GGCGAGGTTGCAGTG | 9690 |
rs74965044 | snp | G/T | 0.0268877 | 0.112787 | intron-variant | UBE3C | GRCh38.p7 | 7:157174908 | GTATATTTTATGTTT[G/T]GCTGTTTCAGATATG | 9690 |
rs74973324 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157190630 | GTGCTCGAGAGCTGT[A/G]TTCTCTATGTCATGG | 9690 |
rs75002046 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | UBE3C | GRCh38.p7 | 7:157179009 | CCCACCAGAGTCCCA[C/G]ATTCCAAAATCTGTC | 9690 |
rs75018238 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137182 | TGACCTCGTGATCTG[C/T]CCGCCTCGGCCTCCC | 9690 |
rs75021852 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157222765 | TGTTGGAAAGGAATG[A/G]GATATGTGTTTATTC | 9690 |
rs75036909 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE3C | GRCh38.p7 | 7:157255442 | CGTATGTATCTCTTA[C/T]CTGTAGTTTGCATTG | 9690 |
rs75088001 | snp | A/C | 0.347694 | 0.230122 | intron-variant | UBE3C | GRCh38.p7 | 7:157154167 | CTCTACTAAAAATGC[A/C]AAAATTAGCCAGGTG | 9690 |
rs75092114 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157146259 | TTTCTTTTTTTTTTT[G/T]GAGACGAAGTCTCGC | 9690 |
rs75121270 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBE3C | GRCh38.p7 | 7:157140099 | TCTGTCCCTGAAGAC[A/G]GGCATCAGTTGGTTC | 9690 |
rs75125615 | snp | A/G | 0.0136262 | 0.081409 | intron-variant | UBE3C | GRCh38.p7 | 7:157201850 | AGCTCAAGGGCACAG[A/G]AAGTGGCAGCCTAAT | 9690 |
rs75125694 | snp | G/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216557 | TTTCCTTCTTTGTGT[G/T]CATGGGTTCTTATCA | 9690 |
rs75126447 | snp | A/C | 0.031825 | 0.122064 | intron-variant | UBE3C | GRCh38.p7 | 7:157145644 | TGTCATATAGTTGGA[A/C]TCATATACTATGTAA | 9690 |
rs75128715 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157223804 | ATGTACCTGTAGTCC[C/T]AGCTACTTGGGATGC | 9690 |
rs75182280 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137263 | TATTTTTTGAGACAG[A/G]GTCTCACTCTGTCAC | 9690 |
rs75194111 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157213582 | TTGTAGAGCAGTTGA[C/G]TTTGTGATTCTGAAA | 9690 |
rs75202555 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157227051 | TCCCACTTGACCCTG[C/G]AGGTCTTTACAGCTT | 9690 |
rs75231497 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157266731 | GATAGAATAAATCTT[A/G]ATCCTTTTTAAAAAA | 9690 |
rs75252575 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137291 | CACCCAGGCTGGAGT[A/G]CAGTGGCACGATCTC | 9690 |
rs75270041 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157222423 | TTACTTTTTTTTTTT[C/T]TTTCTTTCTTTTTTG | 9690 |
rs75273169 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157255841 | TAGTGGTCTCATCAT[A/G]TAGTGAGATTGGTTG | 9690 |
rs75274476 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | UBE3C | GRCh38.p7 | 7:157233220 | GGTTTCATTCATGTC[A/G]TAGTATGTCAGAGCT | 9690 |
rs75371354 | snp | A/G | 0.297636 | 0.24542 | intron-variant | UBE3C | GRCh38.p7 | 7:157254917 | TACACCTGCAGTCCC[A/G]GCGTGGTGGCGTACA | 9690 |
rs75383598 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157268045 | CACTAGTGGCATCTC[A/G]GTGAAATTAACCAAA | 9690 |
rs75478275 | snp | C/T | 0.370568 | 0.219005 | intron-variant | UBE3C | GRCh38.p7 | 7:157163311 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 9690 |
rs75514003 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157253829 | ACTCGGGTACTATTT[C/T]GTATTTAGATTCTTG | 9690 |
rs75540415 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157194792 | GCTAAGCTGAATTGT[A/G]TCCTGCAGTTATGTG | 9690 |
rs75554229 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157146260 | TTCTTTTTTTTTTTT[G/T]AGACGAAGTCTCGCT | 9690 |
rs75556110 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157158051 | TACACTCTTTTTTCC[G/T]TTTTTTTTTTTTTTT | 9690 |
rs75581021 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | UBE3C | GRCh38.p7 | 7:157148919 | CCCAACCCCAGCCTG[C/G]CTCTGAAAATGTTAA | 9690 |
rs75583197 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157172733 | TCAGAATAGTACAAC[C/G]GCAGATAATCGGGCT | 9690 |
rs75594341 | snp | C/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157143966 | AGTGGTGTCCAGGGA[C/G]TGAATCTCAGGGAGG | 9690 |
rs75613129 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | UBE3C | GRCh38.p7 | 7:157140388 | TAAAGAGTTGGGAGA[G/T]AAGTGTGCTGATAAT | 9690 |
rs75656679 | snp | A/C | 0.021333 | 0.101051 | intron-variant | UBE3C | GRCh38.p7 | 7:157258275 | CCTTCAAATAACCTT[A/C]AATCAGAAAGAGTTC | 9690 |
rs75687422 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137303 | AGTACAGTGGCACGA[G/T]CTCAGCTCATTGCAA | 9690 |
rs75721940 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157250102 | GAACAGGGGCAGGAA[C/G]TGGGGCTATCAGTTC | 9690 |
rs75775370 | snp | A/G | 0.031825 | 0.122064 | intron-variant | UBE3C | GRCh38.p7 | 7:157247414 | AGAAAACTTTTGGCC[A/G]GGCAGGATGGCTCAC | 9690 |
rs75788417 | snp | A/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216994 | TGAAAGATCTTTTTA[A/T]TATTTATCATTAAAA | 9690 |
rs75819051 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157252520 | AAAATGTGAAACGTT[A/G]AAAGAAGCAGATCTG | 9690 |
rs75822318 | snp | G/T | 0.0412859 | 0.137617 | intron-variant | UBE3C | GRCh38.p7 | 7:157225563 | AATTCTTTCTGTGTA[G/T]TATTTGGCAGGTGGA | 9690 |
rs75857261 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157146513 | GGCATGAGCCCCTGC[A/G]TCCGGCCTTTACGAT | 9690 |
rs75859293 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE3C | GRCh38.p7 | 7:157265063 | TACAGCTCTTCCTTC[A/G]TTGTGATGCTGTGAA | 9690 |
rs75959926 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157238622 | AGGCATTCTTATGGA[A/G]GCTTAGTGAGGGGCA | 9690 |
rs75981616 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UBE3C | GRCh38.p7 | 7:157259393 | TCGTCAATGTGATGT[C/T]GCAGCCCCACCGTTG | 9690 |
rs75984058 | snp | A/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157218469 | ATAAAAAAAAAAAAC[A/C]ATGTCACAGAAATAT | 9690 |
rs76000864 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157175503 | CATTCAGTGTCCGAA[A/G]GAACACGTGTAAGTG | 9690 |
rs76022699 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157147893 | GGAATAAATCCCACT[C/T]GACTGTGATGCATAA | 9690 |
rs76061151 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE3C | GRCh38.p7 | 7:157201552 | CGTGTCTCGGTGTCT[C/T]ATCAAATGGCTGGTT | 9690 |
rs76065469 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267887 | TTCATTCTGCCATTC[C/T]TCCCTCCCTTCCTTT | 9690 |
rs76110497 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157231925 | ACTCTTTGGGGGGGG[A/G]GGGAGGCTTAGAAAA | 9690 |
rs76129617 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137084 | TGGGACTACAGGCGC[A/C]TGCCACTATGCCTGG | 9690 |
rs76132781 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | UBE3C | GRCh38.p7 | 7:157165150 | GAAAGATATTTGTTG[A/G]TTGGTGTTTTTAATC | 9690 |
rs76142150 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157201660 | TTTTTTTTTTTTTTA[A/G]GAAATGTTTTGAATA | 9690 |
rs76219731 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | UBE3C | GRCh38.p7 | 7:157238619 | GGGAGGCATTCTTAT[A/G]GAGGCTTAGTGAGGG | 9690 |
rs76222662 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157173388 | TTCTCAAGCATAGAT[A/G]CGATAGCAATAAATT | 9690 |
rs76320903 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157241001 | AGAGGTAATGGATGC[A/G]CAAGCCCAGTGCATG | 9690 |
rs76336786 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157222422 | TTTACTTTTTTTTTT[C/T]CTTTCTTTCTTTTTT | 9690 |
rs76382747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157186469 | TGCTTAAACTGTGAT[C/G]TCAAATTAAAATGAA | 9690 |
rs76392319 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE3C | GRCh38.p7 | 7:157175356 | GGACTCCTGATGTGT[A/G]AGAATGATTCCATTC | 9690 |
rs76478297 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157256335 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTGGT | 9690 |
rs76489726 | snp | C/T | 0.0479149 | 0.147179 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269464 | CATGTCACCAGCTAA[C/T]GGAGTATAGTAAGAT | 9690 |
rs76505209 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157259030 | TTTGAAACGGCCACA[A/G]TTAAATTATTACAAG | 9690 |
rs76570838 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157148840 | CAGCAGCCTCAAACT[A/C]CTGATCTCCAGCGAT | 9690 |
rs76600876 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | UBE3C | GRCh38.p7 | 7:157242640 | GGGTTTGCTACTTTA[A/G]CGAACTTCCTTGTTC | 9690 |
rs76618456 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216990 | TTATTGAAAGATCTT[C/T]TTAATATTTATCATT | 9690 |
rs76636874 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | UBE3C | GRCh38.p7 | 7:157190261 | TGTCCCTGGGGACCT[C/T]TCCTCTGTCCCCTCC | 9690 |
rs76641879 | snp | A/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157156730 | AAAAAAAAAAAAAAA[A/C]CACAAGCTAGAGCAT | 9690 |
rs76685584 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137301 | GGAGTACAGTGGCAC[A/G]ATCTCAGCTCATTGC | 9690 |
rs76702370 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | UBE3C | GRCh38.p7 | 7:157216736 | CCCTTTTCTGTGAGC[A/G]GGTTTGGTGTCCGGC | 9690 |
rs76722121 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157159748 | GGCACATGGTAATCC[C/T]GGCGGCGGAGGTTGC | 9690 |
rs76782860 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157227295 | GGGTGAGGGGAGCTC[C/T]GAGGGCACGGGTGCT | 9690 |
rs76861890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE3C | GRCh38.p7 | 7:157225248 | CATTATATATTATCT[A/G]TACATTTATTGATAA | 9690 |
rs76862958 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157239812 | GCTGAAGCAGGGGGC[A/G]CCACAGGCTGCGTGT | 9690 |
rs76874580 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157173921 | CCAGTTTAAGACATG[C/T]GCTAATTTATTATGC | 9690 |
rs76888369 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | UBE3C | GRCh38.p7 | 7:157140209 | ATGTTCTTTAAAATG[C/T]TTCACCTAGTTTTTC | 9690 |
rs77027870 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157186704 | CTAAGTGTACTGTGA[C/T]GTAGATAATTTTGAG | 9690 |
rs77091531 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | UBE3C | GRCh38.p7 | 7:157256547 | GGAGGCAGAGAATTC[C/T]GCTTTTGCATTTACA | 9690 |
rs77093841 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE3C | GRCh38.p7 | 7:157226813 | AGACCGAGTAAACTT[A/C]GGTCTGCATGCAGGC | 9690 |
rs77100778 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157197524 | GTTTTTTTTTTTTTT[A/T]AATGCTGGAGGTATT | 9690 |
rs77116802 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157171427 | GCCACCATGCCCAGC[C/T]TTAGGGTCTCATGTT | 9690 |
rs77230107 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | UBE3C | GRCh38.p7 | 7:157183108 | AGCAGAAATGTGGGG[G/T]TTTTTTTCCCACACA | 9690 |
rs77238165 | in-del | -/TT | 0.0799831 | 0.183287 | intron-variant | UBE3C | GRCh38.p7 | 7:157206131 | GAGGGGACCATGGAC[-/TT]TATAGAAAGAGCTTG | 9690 |
rs77259861 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157158072 | TTTTTTTTTTTTTTT[C/T]CCTGTAAAGGGAGCC | 9690 |
rs77292122 | snp | C/G | 0.093417 | 0.194889 | intron-variant | UBE3C | GRCh38.p7 | 7:157243605 | CCTCCTGCTGCTGTT[C/G]CTGCATGTGAGGCGC | 9690 |
rs77306274 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE3C | GRCh38.p7 | 7:157242116 | ATAAAACCTTTGAAT[A/G]TAAGTTATGTGGGTG | 9690 |
rs77315883 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267947 | CTTATTTAGATGGAC[A/G]TTGCTTTTCAAATAA | 9690 |
rs77330736 | snp | A/C | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157246015 | AAAAAAAAAAAAAAA[A/C]AGTGTTCTTCACAAT | 9690 |
rs77339024 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE3C | GRCh38.p7 | 7:157202289 | GTATGTAATAGGTAG[A/G]AATTTCATACTTAAA | 9690 |
rs77344990 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBE3C | GRCh38.p7 | 7:157149706 | GTTGAAAAAATAGAT[A/G]GTCTCATAAGACCAT | 9690 |
rs77354933 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE3C | GRCh38.p7 | 7:157258277 | TTCAAATAACCTTCA[A/G]TCAGAAAGAGTTCCT | 9690 |
rs77446617 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157160899 | ATTGAGTCCATGATG[A/C]GTGTTTGTGCGTATA | 9690 |
rs77447584 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE3C | GRCh38.p7 | 7:157147768 | AAGGTTGGGTTTTGT[C/T]AGATGCTTTTTCTGT | 9690 |
rs77455419 | snp | A/G | 0.329317 | 0.237084 | intron-variant | UBE3C | GRCh38.p7 | 7:157167589 | GTCACCCAGGCTGGA[A/G]TGCAGTGGCGCGATC | 9690 |
rs77471740 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157171699 | ATATTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTTTT]GAGACAGAGTCTTGC | 9690 |
rs77519464 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157230941 | AAAAATAATGATAAT[A/G]TCATTGCTGTTTTGA | 9690 |
rs77540550 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157203799 | ATTAATGCGTTCCCA[A/G]TACAGATACTCCTTG | 9690 |
rs77608824 | snp | C/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157267637 | CCGACCTTGAGCGGC[C/T]CCCCACAGCCAGCAC | 9690 |
rs77621382 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157208060 | ATTTGCAAGACTTTT[A/T]TTTTTTTTTTTTTTT | 9690 |
rs77653755 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBE3C | GRCh38.p7 | 7:157246467 | GATGGCCTCTAGGTT[A/G]GAAGGGTGACTTCTG | 9690 |
rs77681964 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216561 | CTTCTTTGTGTTCAT[A/G]GGTTCTTATCATGTA | 9690 |
rs77708214 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157257193 | ACTGGTTATGATGTA[G/T]ATATTTTGGTGCTAG | 9690 |
rs77723195 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157258193 | CCCAAGAAATCCTCT[C/T]ACTTCAGCCTCCCAA | 9690 |
rs77725858 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157162556 | ACTTTTTTTTTTTTT[G/T]TGAGACAGGATCTTG | 9690 |
rs77735825 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157258882 | AACCCGCACTGACCA[A/G]TTGTTAACATTTTGC | 9690 |
rs77749234 | in-del | -/AACT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157188772 | AAGTAGGCTTACTCT[-/AACT]GTTACAGATTTTAAC | 9690 |
rs77754019 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157259655 | ATATGTAATTCCACT[C/T]GGATAAACTGTCCTT | 9690 |
rs77756029 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | UBE3C | GRCh38.p7 | 7:157176003 | GCTTCACTCAACAGC[C/T]GTACAAAAAACAGCC | 9690 |
rs77803471 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157200474 | AAAGACCTCATCTCT[A/T]AAAAAAATATTTATG | 9690 |
rs77809691 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137313 | CACGATCTCAGCTCA[C/T]TGCAACCTCCGCCTC | 9690 |
rs77816935 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157204293 | AGGACTTACAGCTTT[A/T]GTGGGCAGAAGTATC | 9690 |
rs77925601 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | UBE3C | GRCh38.p7 | 7:157266452 | AGGTAATGTCGTATG[C/T]TTCCCATTCCCTTAA | 9690 |
rs77943122 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | UBE3C | GRCh38.p7 | 7:157218865 | TAACTCTGAGTTCGC[A/G]AGGGTGCTAACAAAA | 9690 |
rs77951582 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157259210 | GTGGGAGCGGAGCCC[C/T]GCAGTCACGTTGTGA | 9690 |
rs77958097 | snp | A/G | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157191602 | TGCGCCCAGCCCCTC[A/G]TGTGTTTTCTAACCA | 9690 |
rs77976463 | snp | A/G | 0.031825 | 0.122064 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157136991 | GGAGTGCAGTGGCGC[A/G]AGTGGCGCGATCTCG | 9690 |
rs77992510 | snp | A/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157153843 | AAACAAACAAACAAA[A/C]AAACGGGCATGGTGG | 9690 |
rs78004192 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157269063 | ACAATGAACATTATC[A/G]AAACAAAATGTATAA | 9690 |
rs78015355 | snp | A/C/G | 0.00238783 | 0.0344858 | synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157178759 | GCTTGAAGTATTTTC[A/C/G]TCTGAGAATACTTAC | 9690 |
rs78094926 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | UBE3C | GRCh38.p7 | 7:157180953 | TCCTAAAGCCCACCC[C/T]GGGGCCCCAGGTGGA | 9690 |
rs78097065 | snp | A/C | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216996 | AAAGATCTTTTTAAT[A/C]TTTATCATTAAAAAA | 9690 |
rs78123578 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157158043 | CCAATCTGTACACTC[C/T]TTTTTCCTTTTTTTT | 9690 |
rs78149092 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157173344 | TCCTGCGACTGCACT[C/G]CAGCCTGGGCGGTTG | 9690 |
rs78185185 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157231604 | TCATGTGAGCTCGGC[C/T]GTCATGAATGGATGA | 9690 |
rs78188573 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE3C | GRCh38.p7 | 7:157172743 | ACAACGGCAGATAAT[C/T]GGGCTTGCTTTCTGG | 9690 |
rs78225428 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157183732 | ACAAAATCTAAATAT[A/G]TTTCCTATTATAACA | 9690 |
rs78226408 | snp | A/G | 0.021333 | 0.101051 | intron-variant | UBE3C | GRCh38.p7 | 7:157142435 | GCAATTAAAAATTAA[A/G]TAACAATAGAGTAAT | 9690 |
rs78250632 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157197399 | TCAACTAAAAACTCA[A/G]ACATACTTATCTTAA | 9690 |
rs78274219 | snp | A/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157216942 | CCAAACCACTGGCTG[A/T]CAGAACAAGAAGATA | 9690 |
rs78403696 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | UBE3C | GRCh38.p7 | 7:157212560 | ATCTTGTGAAAACAG[C/T]GCCTGTTAATTTACA | 9690 |
rs78443184 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | UBE3C | GRCh38.p7 | 7:157267009 | GCCTCCCAAAGTGCT[A/G]GGACTACAGGTGTGA | 9690 |
rs78452976 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | UBE3C | GRCh38.p7 | 7:157165245 | CCTCTCCTACTTGGA[C/T]GCAAACTGTAAATGT | 9690 |
rs78463056 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | UBE3C | GRCh38.p7 | 7:157165322 | CTGTGTTTATCCTTT[C/T]GAATATCTCTGCTTC | 9690 |
rs78465153 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157257961 | CTTTTTTTTTTTTTT[A/T]AAGTAAGATGAGCAC | 9690 |
rs78465844 | snp | A/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157218467 | AAATAAAAAAAAAAA[A/C]CCATGTCACAGAAAT | 9690 |
rs78543956 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | UBE3C | GRCh38.p7 | 7:157214676 | AAAGATTGTACTTCT[G/T]TTCCTTTTAGAAGGG | 9690 |
rs78558289 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157174861 | TGGGGTATTATGTAA[A/G]TTAGCAAACTATTAA | 9690 |
rs78580906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157247420 | CTTTTGGCCGGGCAG[A/G]ATGGCTCACACCTAT | 9690 |
rs78643512 | snp | A/C | 0.029116 | 0.117091 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157138016 | TGTATACAACCAAAA[A/C]TCAATTTTTAGAAAT | 9690 |
rs78646781 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | UBE3C | GRCh38.p7 | 7:157237768 | CTAAAAAATAGTGTT[A/G]GGTGCAGTAGCTCAT | 9690 |
rs78665025 | snp | C/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157193662 | CTTCAGAAATTTGTC[C/T]TTTTTTTTTTTTTTT | 9690 |
rs78719312 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBE3C | GRCh38.p7 | 7:157187299 | ATTCACCCATCTGAA[A/G]GGCTGGACTCATACC | 9690 |
rs78745954 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137233 | GTGAGCCACCGCGCC[C/T]GGCCTGTTTATTTTT | 9690 |
rs78746742 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137264 | ATTTTTTGAGACAGA[A/G]TCTCACTCTGTCACC | 9690 |
rs78748294 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157157052 | CGGTAGGAGGAAAAA[A/T]TAAAGGTGTAGGCAT | 9690 |
rs78847259 | snp | G/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157162507 | CTAAATTTATTTTTT[G/T]GTAATGATTCATATA | 9690 |
rs78854960 | in-del | -/TA | | | intron-variant | UBE3C | GRCh38.p7 | 7:157157987 | AGATATATATATATA[-/TA]GAGAGAGAGAGAGAG | 9690 |
rs78883126 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157216993 | TTGAAAGATCTTTTT[A/G]ATATTTATCATTAAA | 9690 |
rs78888464 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137308 | AGTGGCACGATCTCA[A/G]CTCATTGCAACCTCC | 9690 |
rs78930357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157265700 | TCCAATGTGCTCACC[A/G]TCTCAATTTTAAACC | 9690 |
rs78946200 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | UBE3C | GRCh38.p7 | 7:157245906 | TGAGACAGGAGAATC[A/C/G]CTTGAACTCGGGAGG | 9690 |
rs78947531 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157236682 | TGCCTTAGTCCTTAA[A/T]GGGGCAGAGCTTCTC | 9690 |
rs78971850 | snp | A/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157230409 | TGAAAAAAAAAAAAA[A/T]TTACAGGCCGGGCAC | 9690 |
rs78979825 | snp | C/T | 0.386694 | 0.20932 | intron-variant | UBE3C | GRCh38.p7 | 7:157251970 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAA | 9690 |
rs79017747 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBE3C | GRCh38.p7 | 7:157263919 | CCTACATGAGTGTGT[A/G]TTAATGTAGATATGC | 9690 |
rs79055384 | in-del | -/AAAAG | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208396 | ACCTTTTTAATTAAG[-/AAAAG]TAATTTTAGTACTTT | 9690 |
rs79062849 | snp | A/G | 0.347473 | 0.230215 | intron-variant | UBE3C | GRCh38.p7 | 7:157163170 | GCGGGTGGATCAGGA[A/G]GTCAGGAGATCGAGA | 9690 |
rs79078444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157265629 | GCCTCACCATTAATA[A/G]GCAAGATGAGCGAGA | 9690 |
rs79150719 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137272 | AGACAGAGTCTCACT[C/G]TGTCACCCAGGCTGG | 9690 |
rs79206673 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157180961 | CCCACCCCGGGGCCC[C/T]AGGTGGAGCAGCATG | 9690 |
rs79233199 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBE3C | GRCh38.p7 | 7:157166404 | TTTTTCTGACTTCTT[C/T]GTATTTTTCAGAATT | 9690 |
rs79306078 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE3C | GRCh38.p7 | 7:157190266 | CTGGGGACCTCTCCT[C/T]TGTCCCCTCCCAGGG | 9690 |
rs79320422 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157212788 | TTCTTTTTGAGACAG[C/G]GTTTCGTTCTGTTGC | 9690 |
rs79334890 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE3C | GRCh38.p7 | 7:157240799 | GATCAGAGGGGCTTA[G/T]TTACCGGTAATGCCA | 9690 |
rs79335485 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE3C | GRCh38.p7 | 7:157165859 | AGTAATTGGATCTTC[C/T]GTGGGGTTTGTTTCT | 9690 |
rs79345516 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157146248 | TTATGGATCTATTTC[C/T]TTTTTTTTTTTGAGA | 9690 |
rs79477401 | snp | A/G | 0.353803 | 0.227431 | intron-variant | UBE3C | GRCh38.p7 | 7:157252065 | CTCTTGAACCCAGAT[A/G]GTGGAGGTTGCACTG | 9690 |
rs79488584 | snp | C/T | 0.028768 | 0.116432 | intron-variant | UBE3C | GRCh38.p7 | 7:157159476 | ATTCAAAAGATCAGA[C/T]TGTGGATGGTTTCTT | 9690 |
rs79516096 | in-del | -/A | 0.409273 | 0.192697 | intron-variant | UBE3C | GRCh38.p7 | 7:157144690 | TCCAGTGCTTTTTTT[-/A]AAAAAAAAATAGACT | 9690 |
rs79528142 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | UBE3C | GRCh38.p7 | 7:157224075 | AAGCAGTGCTGTGAT[C/G]ATAGCTCACAGCAGC | 9690 |
rs79554102 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157227701 | GAGACTTCATCTCAG[A/G]AAAAAAAAAGAAAAA | 9690 |
rs79555992 | in-del | -/A | | | intron-variant | UBE3C | GRCh38.p7 | 7:157236248 | CTTGAACTTTTTTTT[-/A]ACAGATAGAAGCACC | 9690 |
rs79558287 | snp | C/T | | | missense, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157223265 | TTAGTGGGTTTGGAG[C/T]CCCCGCCGCTGTCTG | 9690 |
rs79635349 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269689 | GTTTGCCCTTTTCTA[C/T]GTTCTGTCCTACTTT | 9690 |
rs79641264 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157253891 | ACATTTGTTTCTTGC[C/T]TTTTTTTTTAACCTA | 9690 |
rs79667166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157215092 | CCACAAGAGAATCGC[C/T]ACTTCTAAATTGGCA | 9690 |
rs79674821 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | UBE3C | GRCh38.p7 | 7:157266996 | ATCCCCCAGCTAGGC[C/T]TCCCAAAGTGCTGGG | 9690 |
rs79685381 | snp | A/G | 0.00795532 | 0.062565 | downstream-variant-500B | UBE3C | GRCh38.p7 | 7:157269511 | GAATCAGAGGTCCTC[A/G]GGAGGATGCCTGTCA | 9690 |
rs79689239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE3C | GRCh38.p7 | 7:157157188 | GAATTAAAAAATTCA[A/G]TATACAGAAATCCAT | 9690 |
rs79709183 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157256252 | GGGAGGCTGAGGCAG[A/G]AGAACTGCTTGAACC | 9690 |
rs79730306 | snp | A/C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157158042 | CCCAATCTGTACACT[A/C/T]TTTTTTCCTTTTTTT | 9690 |
rs79772278 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | UBE3C | GRCh38.p7 | 7:157226465 | TTGGTCAATGCCGAG[A/G]GGATTAAAATGAAAG | 9690 |
rs79797367 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157180158 | GCAGTTGTTTACTTT[C/G]TAACAGTCGATAAAA | 9690 |
rs79806701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE3C | GRCh38.p7 | 7:157225288 | TTTGATACCTTGACT[A/G]TTAGCATTTATTTCA | 9690 |
rs79812505 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157183811 | GTGAGGAAAAATGGC[A/G]TCTTCGTTTTCCATT | 9690 |
rs79848270 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | UBE3C | GRCh38.p7 | 7:157210808 | CCATTTTCATTTTTC[A/G]GTCCTATCATGGTCC | 9690 |
rs79888576 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | UBE3C | GRCh38.p7 | 7:157255044 | CTGGAGGTGGGAGAC[A/G]GAGGTCGTGAGATCT | 9690 |
rs79979561 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | UBE3C | GRCh38.p7 | 7:157228226 | GTGGAATGCAGAGAT[A/T]GATGGCTGTTCCTGC | 9690 |
rs79989576 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | UBE3C | GRCh38.p7 | 7:157142691 | CCAGGGACTACTAGA[A/G]GGGGAAAGAGAGGGA | 9690 |
rs80062807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157251151 | ATCTTAAGGATTTCT[C/G]TAGAAATAAATAGGT | 9690 |
rs80080246 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157233744 | TTTTCTTGGGCATAT[A/G]CCTAGACATGGAAGT | 9690 |
rs80082875 | snp | G/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157170992 | GCTAATTTTTTTTTT[G/T]GTAGAGATGAGGTCT | 9690 |
rs80084785 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157223601 | GATTTCTTATAATGA[A/G]GGTCTAACGTCATTT | 9690 |
rs80093311 | in-del | -/TTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157177942 | CTGTTTTTTTTTTTT[-/TTT]AAGAAAAAGGAAAAA | 9690 |
rs80106199 | snp | A/G | 0.0666844 | 0.169986 | intron-variant | UBE3C | GRCh38.p7 | 7:157217006 | TTAATATTTATCATT[A/G]AAAAATACATTCAGC | 9690 |
rs80138126 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | UBE3C | GRCh38.p7 | 7:157174059 | GCGTATTTATGACTA[A/G]CTACACTTAAGAGGC | 9690 |
rs80173821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157197417 | ATACTTATCTTAAGG[C/T]CTATTCCTAATCCAG | 9690 |
rs80193854 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | UBE3C | GRCh38.p7 | 7:157206083 | TGATCTTGCTCACAG[A/T]GTCTGTTAACCTGTG | 9690 |
rs80195105 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBE3C | GRCh38.p7 | 7:157249614 | CACCGTGGCCGGCAC[A/G]ACAGAGCCTTTTACG | 9690 |
rs80243174 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137249 | GGCCTGTTTATTTTT[A/C]TTTTTTGAGACAGAG | 9690 |
rs80271872 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3C | GRCh38.p7 | 7:157150485 | CTAATATGCATAAGA[A/G]AAGATGCATGGGAAA | 9690 |
rs80283192 | in-del | -/TTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | UBE3C | GRCh38.p7 | 7:157208071 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTT]GATACATGGACTTGA | 9690 |
rs80295032 | snp | A/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157158855 | CTCCAAGTGTGTTGA[A/G]TGGTAAAAGCAGAGA | 9690 |
rs80309594 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | UBE3C | GRCh38.p7 | 7:157222749 | CCAAGTTACGATTTA[G/T]TGTTGGAAAGGAATG | 9690 |
rs80352141 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | UBE3C | GRCh38.p7 | 7:157222607 | AAAAAAATTTTCTTC[A/G]TAGAGGCAAGGTCTC | 9690 |
rs111265760 | snp | A/C | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264496 | GGTACTACAGGTGTG[A/C]GCCAACATGCTCGGC | 9690 |
rs111284106 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE3C | GRCh38.p7 | 7:157154005 | CTGTCTGGGGGGGGA[A/G]AAGTTAACTTTTTCT | 9690 |
rs111288330 | snp | C/G | | | intron-variant | UBE3C | GRCh38.p7 | 7:157163182 | GGAGGTCAGGAGATC[C/G]AGACCATCCTGGCTA | 9690 |
rs111303657 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | UBE3C | GRCh38.p7 | 7:157169853 | AGCTGGCTAAATGTT[C/T]TTGTATTTTTAGTAG | 9690 |
rs111320647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157177259 | TTACTAATGATGACG[A/G]GTGTTTCTCAGGAGC | 9690 |
rs111354490 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | UBE3C | GRCh38.p7 | 7:157142106 | GTTTCTTTGTGGTTT[C/T]AATTTTGTTTCCTGA | 9690 |
rs111359026 | snp | C/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157148841 | AGCAGCCTCAAACTC[C/G]TGATCTCCAGCGATT | 9690 |
rs111368151 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157155709 | CTTGGTAAGACAAAA[C/T]GAAAAGAAAATCACC | 9690 |
rs111370006 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157168007 | AGAAAGTGACCTTTA[A/C]AATAGATGCTGGTGT | 9690 |
rs111389766 | snp | A/C/T | 0.00575161 | 0.0533179 | missense, synonymous-codon, nc-transcript-variant | UBE3C | GRCh38.p7 | 7:157253971 | AGTTGAACTAAAATT[A/C/T]GGTGGGAAAGACATC | 9690 |
rs111443798 | in-del | -/T | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157246899 | ACTGGATATTTTCTC[-/T]TTTTTTTGAGACGGA | 9690 |
rs111457351 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE3C | GRCh38.p7 | 7:157206453 | ATCTTTAGTAGAGAT[A/G]GGGTTTCACCATGTT | 9690 |
rs111483990 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | UBE3C | GRCh38.p7 | 7:157221428 | TCCTCATCAGCACTT[A/C]CAGTTGTCATTTAAA | 9690 |
rs111496969 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | UBE3C | GRCh38.p7 | 7:157225750 | GCTCAGGAGTTAGAG[A/G]CCAGCCTGGGCAACA | 9690 |
rs111569260 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157173772 | GGACGAACTACATGT[C/T]AGATGGTGAAGGGAG | 9690 |
rs111613223 | in-del | -/AC | 0.401761 | 0.198667 | intron-variant | UBE3C | GRCh38.p7 | 7:157264297 | CATGCTTGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs111673497 | in-del | -/TT | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157207952 | TATAGAGTATATGTA[-/TT]TTTTTGTTTACTGAC | 9690 |
rs111680597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157237435 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAG | 9690 |
rs111754592 | snp | A/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157156562 | TCCACTACCCTGGCC[A/T]CCAAAACTGCTAGCG | 9690 |
rs111756064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE3C | GRCh38.p7 | 7:157216573 | CATGGGTTCTTATCA[C/T]GTAGCTCCCGCCAAA | 9690 |
rs111792062 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157144847 | TGATAAACCAATGTC[A/G]ATGTGTTATTATTAA | 9690 |
rs111811184 | snp | G/T | | | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137111 | CTGGCTAATTTTTTT[G/T]GTATTTTTAGTAGAG | 9690 |
rs111832463 | snp | A/G | 0 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157244123 | TAATCCCAGCTGCTC[A/G]CGAGGCTGAGGCAGG | 9690 |
rs111900340 | snp | A/T | 0.118933 | 0.212888 | intron-variant | UBE3C | GRCh38.p7 | 7:157262470 | TGTTGCCCAGGCTGG[A/T]GTACAATGGCCCATC | 9690 |
rs111902520 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE3C | GRCh38.p7 | 7:157200774 | TGAGTAGCTGGGACT[A/G]CAGCCACCACACCCA | 9690 |
rs111910140 | snp | C/T | 0.444444 | 0.157135 | intron-variant | UBE3C | GRCh38.p7 | 7:157184293 | GATCATACTATATGT[C/T]AACTTAGTTATTAGG | 9690 |
rs111931766 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157230609 | CTGAGGCAGAAGAAT[C/T]ACTTGAACCCGGGAG | 9690 |
rs111984524 | in-del | -/AC | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264406 | CATGCTCGGCCTGTT[-/AC]ACACACACACACACA | 9690 |
rs112010840 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE3C | GRCh38.p7 | 7:157159043 | CACTCCTGTGAAAGG[C/T]GGAGACTTAATTCTC | 9690 |
rs112012369 | snp | C/T | | | intron-variant | UBE3C | GRCh38.p7 | 7:157267346 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 9690 |
rs112015949 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE3C | GRCh38.p7 | 7:157192136 | AAATAGACTTGCCTT[C/T]GTCAGCTTCAGCAAT | 9690 |
rs112047917 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE3C | GRCh38.p7 | 7:157266444 | CATCACATAGGTAAT[A/G]TCGTATGCTTCCCAT | 9690 |
rs112090183 | snp | A/G | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157215162 | GAGTGGGTTTTTACT[A/G]TGCAGTTTTATCTGC | 9690 |
rs112096000 | snp | A/T | 0.128976 | 0.218754 | upstream-variant-2KB | UBE3C | GRCh38.p7 | 7:157137744 | TAAGTTTTGTATTTT[A/T]TTAGAGATGGGGTTT | 9690 |
rs112123453 | snp | C/T | 0.5 | 0 | intron-variant | UBE3C | GRCh38.p7 | 7:157264388 | TACTACAGGTGTGAG[C/T]CAACATGCTCGGCCT | 9690 |