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 |