SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs52481 | snp | A/T | 0 | 0 | intron-variant | UBE3D | GRCh38.p7 | 6:82900113 | AGGGAACAGTGGCAC[A/T]GCTGCAGCTTTGGCC | 90025 |
rs159040 | snp | A/G | 0.498982 | 0.0225409 | intron-variant, downstream-variant-500B | UBE3D | GRCh38.p7 | 6:82892158 | ACATCCTCCTTTCCT[A/G]CTCCAGGATCAGGAG | 90025 |
rs159048 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE3D | GRCh38.p7 | 6:82895399 | tgtgtactgacgggc[A/G]tttggcagtatctgg | 90025 |
rs159049 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | UBE3D | GRCh38.p7 | 6:82895435 | ttttcggttgtcaac[A/G]taactgggagggggt | 90025 |
rs159050 | snp | C/G | 0.495135 | 0.0490805 | intron-variant | UBE3D | GRCh38.p7 | 6:82896438 | AAGACAACCTTTCCT[C/G]TCGGTTATAAGATCT | 90025 |
rs159051 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | UBE3D | GRCh38.p7 | 6:82896974 | TCGAACTCCTGACCT[C/T]GTGATCCACCCGCCC | 90025 |
rs159052 | snp | C/T | 0.118235 | 0.212457 | intron-variant | UBE3D | GRCh38.p7 | 6:82897638 | ACAAAATCTAGTTTC[C/T]AAGATCCAAATTTCC | 90025 |
rs159053 | snp | C/T | 0.121369 | 0.214369 | intron-variant | UBE3D | GRCh38.p7 | 6:82901002 | TGATTTATGATTATA[C/T]GAATTATAGACAAAC | 90025 |
rs159054 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | UBE3D | GRCh38.p7 | 6:82901120 | ATTTCTAGATTTCTA[C/T]TTTTCTGGACAATTC | 90025 |
rs159055 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | UBE3D | GRCh38.p7 | 6:82901893 | TGAATTTGAGATATT[A/G]GCCCCTTCAGTCTCT | 90025 |
rs159056 | snp | C/T | 0.121369 | 0.214369 | intron-variant | UBE3D | GRCh38.p7 | 6:82902078 | GTCACTCCACATGGG[C/T]CTCCAGCAAATTTAC | 90025 |
rs159057 | snp | A/G | 0.117886 | 0.21224 | intron-variant | UBE3D | GRCh38.p7 | 6:82902475 | caatacacatgactc[A/G]gaagaatctctaggg | 90025 |
rs169789 | snp | A/G | 0.43598 | 0.167067 | intron-variant | UBE3D | GRCh38.p7 | 6:82943278 | tgtcagggggaCAGT[A/G]GATAGGGTATTCtaa | 90025 |
rs184133 | snp | C/T | 0.424037 | 0.179474 | intron-variant | UBE3D | GRCh38.p7 | 6:82961376 | AATATAACTAAAGTG[C/T]CTGACCTGGTGCCTG | 90025 |
rs188378 | snp | C/T | 0.432797 | 0.170544 | intron-variant | UBE3D | GRCh38.p7 | 6:82928951 | ATAATGCAGAATAAT[C/T]GATTAAGGTGTTTGT | 90025 |
rs190889 | snp | C/T | 0.442385 | 0.15965 | intron-variant, utr-variant-3-prime | UBE3D | GRCh38.p7 | 6:82944271 | ctgtcatactgtggc[C/T]gagctagtattcaag | 90025 |
rs192666 | snp | G/T | 0 | 0 | intron-variant | UBE3D | GRCh38.p7 | 6:82893441 | TATCACAATGACCTA[G/T]GAGAGACTGGTATAA | 90025 |
rs293482 | snp | A/T | 0.425586 | 0.17796 | intron-variant | UBE3D | GRCh38.p7 | 6:82971599 | CTGTCTCAATATTTT[A/T]AAAAAAAGAAAACAT | 90025 |
rs293483 | snp | G/T | 0.422787 | 0.180679 | intron-variant | UBE3D | GRCh38.p7 | 6:82971060 | GGGGTCCATAAATCT[G/T]GAAAACATTATGCTA | 90025 |
rs293484 | snp | G/T | 0.421051 | 0.182323 | intron-variant | UBE3D | GRCh38.p7 | 6:82970875 | AGTCCCTAGTTTTTG[G/T]TTTTTGTTTTTTGTT | 90025 |
rs293485 | snp | A/G | 0.249886 | 0.25 | intron-variant | UBE3D | GRCh38.p7 | 6:82967834 | ataatatagtgatcc[A/G]tctcttaaatttttt | 90025 |
rs293486 | snp | A/G | 0.20111 | 0.245173 | intron-variant | UBE3D | GRCh38.p7 | 6:82964980 | TGGCATTTGTAATTT[A/G]AAAGGGTCAAATTTT | 90025 |
rs293487 | snp | A/G | 0.433236 | 0.170072 | intron-variant, utr-variant-3-prime | UBE3D | GRCh38.p7 | 6:82912588 | AAGCGGAATATAAAA[A/G]ACCTATCAAGAGCTT | 90025 |
rs293488 | snp | A/G | 0.433382 | 0.169915 | intron-variant, utr-variant-3-prime | UBE3D | GRCh38.p7 | 6:82912768 | CACTCATACATCCAC[A/G]TAGTCATCCTCTGGA | 90025 |
rs293489 | snp | A/T | 0.434109 | 0.169127 | intron-variant | UBE3D | GRCh38.p7 | 6:82912968 | TGAGGAGCCACAGTA[A/T]CAATAAACCTACCTG | 90025 |
rs293490 | snp | G/T | 0.435119 | 0.16802 | intron-variant | UBE3D | GRCh38.p7 | 6:82914538 | CTGCTTGACGCCGAG[G/T]TGCCACAGTAGAGTC | 90025 |
rs293491 | snp | A/T | 0.432797 | 0.170544 | intron-variant | UBE3D | GRCh38.p7 | 6:82914724 | AAAATAATTTATAGC[A/T]TTCTGCAAAGAGCCC | 90025 |
rs293492 | snp | A/G | 0.432944 | 0.170387 | intron-variant | UBE3D | GRCh38.p7 | 6:82915423 | GTCTGTACAAAATTC[A/G]AGTATAAATATTAAA | 90025 |
rs293493 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82915853 | ACTGATATTTGCATC[A/G]CTTCCTGCTCTACCT | 90025 |
rs293494 | snp | C/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82918006 | CCTTCAATAAACTCC[C/T]TGCTCTTTATTTTCC | 90025 |
rs293495 | snp | A/C | 0.276267 | 0.248616 | intron-variant | UBE3D | GRCh38.p7 | 6:82918290 | CAACAACAACAACAA[A/C]AAAAAAAAAACAAAA | 90025 |
rs293496 | snp | G/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82919099 | CTTTCTAAACATGGG[G/T]GAAGAGGAAGAAAGT | 90025 |
rs293497 | snp | G/T | 0.26326 | 0.249648 | intron-variant | UBE3D | GRCh38.p7 | 6:82920266 | TAACAAATGTGTTTT[G/T]GGATATGACATCCAG | 90025 |
rs293498 | snp | G/T | 0.266 | 0.249487 | intron-variant | UBE3D | GRCh38.p7 | 6:82920872 | AAGAAAAGATTTAAC[G/T]CCCATTTTTTCCAGT | 90025 |
rs293499 | snp | G/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82922201 | GAAATTATTGAAACT[G/T]ATTCCAGAATAAATA | 90025 |
rs293500 | snp | A/G | 0.221737 | 0.248397 | intron-variant | UBE3D | GRCh38.p7 | 6:82922605 | atcaaagacttaaac[A/G]taagacctaggacca | 90025 |
rs293501 | snp | C/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82923092 | gtggagaaataggaa[C/T]gcttttacactgttg | 90025 |
rs293502 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82923528 | aacacatggacacag[A/G]gaggggaacatcaca | 90025 |
rs293503 | snp | A/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82923946 | GCCTAGAGTCAAAAG[A/T]AAAAAAACAAATTTC | 90025 |
rs293504 | snp | C/T | 0.26518 | 0.249539 | intron-variant | UBE3D | GRCh38.p7 | 6:82925410 | CAAAAGCCAGAAAAC[C/T]TGTTTCTTCAACCTT | 90025 |
rs293505 | snp | C/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82926518 | taagaaattgccaac[C/G]tgttttctaaagtgg | 90025 |
rs293506 | snp | C/T | 0.280785 | 0.248097 | intron-variant | UBE3D | GRCh38.p7 | 6:82927227 | ctttttttttttttt[C/T]ccccaccaataccac | 90025 |
rs293507 | snp | G/T | 0.221737 | 0.248397 | intron-variant | UBE3D | GRCh38.p7 | 6:82933814 | TCTGAGTATAGCTAT[G/T]AGTTGGAATTCTCTC | 90025 |
rs293508 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82933352 | TTTCATGACAGTAAA[A/G]CTGGCTCACTATTCA | 90025 |
rs293509 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82932594 | TTCATGGAGGGCAAA[A/G]CAGACCAAGAAAAAC | 90025 |
rs293510 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82932525 | GGGTGATTTGGAATC[A/G]CCACCAGAAAGATTA | 90025 |
rs293511 | snp | C/T | 0.26326 | 0.249648 | intron-variant | UBE3D | GRCh38.p7 | 6:82932191 | taataaagacatacc[C/T]gagagtaggtaattt | 90025 |
rs293512 | snp | C/T | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82930874 | tctccttgtttctca[C/T]gcaaatttctgcagt | 90025 |
rs293513 | snp | C/T | 0.432651 | 0.170701 | intron-variant | UBE3D | GRCh38.p7 | 6:82930778 | ttaaacttttatgct[C/T]tgcttcctgttaaac | 90025 |
rs293514 | snp | C/T | 0.431769 | 0.17164 | intron-variant | UBE3D | GRCh38.p7 | 6:82930250 | actcacagttcagca[C/T]gactggggaggcctc | 90025 |
rs293515 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82929384 | TTTTGACAATTAAGG[A/G]ACAAATTAAGGGCTT | 90025 |
rs293516 | snp | C/T | 0.434687 | 0.168495 | intron-variant | UBE3D | GRCh38.p7 | 6:82952356 | accaatcactgagaa[C/T]ggtacctggaaaaca | 90025 |
rs293517 | snp | C/T | 0.450859 | 0.148847 | intron-variant | UBE3D | GRCh38.p7 | 6:82952736 | GAGAAATGCTAAGTA[C/T]AGAAAAATCCCCTCT | 90025 |
rs293518 | snp | G/T | 0.221141 | 0.248329 | intron-variant | UBE3D | GRCh38.p7 | 6:82953633 | CCCATCCAGCCATCT[G/T]GCCAGCCATCCAATA | 90025 |
rs293519 | snp | C/T | 0.44252 | 0.159487 | intron-variant | UBE3D | GRCh38.p7 | 6:82953778 | AGGTGAACAAATAAA[C/T]GAACAAGATCAAATA | 90025 |
rs293520 | snp | A/G | 0.445739 | 0.166827 | intron-variant | UBE3D | GRCh38.p7 | 6:82954009 | AGCCAGAACCAGCTC[A/G]TGATAAGGACAGGGA | 90025 |
rs293521 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE3D | GRCh38.p7 | 6:82942394 | tctgcagccagcttg[C/T]attttttcccagaat | 90025 |
rs293522 | snp | C/T | 0.442113 | 0.159977 | intron-variant | UBE3D | GRCh38.p7 | 6:82942022 | gttccaacctctgcc[C/T]gtttcccagttccaa | 90025 |
rs293523 | snp | A/G | 0.236434 | 0.249632 | intron-variant | UBE3D | GRCh38.p7 | 6:82940542 | CGTGTGCATCCCAGG[A/G]AACTGAGATGGGAGT | 90025 |
rs293524 | snp | A/C | 0.438666 | 0.164028 | intron-variant | UBE3D | GRCh38.p7 | 6:82940140 | GAGGATGGGGCCAGG[A/C]AGACAGCCTGGAGGT | 90025 |
rs293525 | snp | A/G | 0.431177 | 0.172264 | intron-variant | UBE3D | GRCh38.p7 | 6:82939378 | GTACCCACGATAGAC[A/G]ATGTGGTATGGGTTT | 90025 |
rs293526 | snp | A/G | 0.431473 | 0.171952 | intron-variant | UBE3D | GRCh38.p7 | 6:82938337 | GGCACGTCTGATGTG[A/G]TAGGACAGTCGCTCA | 90025 |
rs293527 | snp | A/G | 0.431473 | 0.171952 | intron-variant | UBE3D | GRCh38.p7 | 6:82938135 | TTCCCAGCTGTTCCT[A/G]ATTTATTCACCCAGT | 90025 |
rs293528 | snp | G/T | 0.431325 | 0.172108 | intron-variant | UBE3D | GRCh38.p7 | 6:82937469 | TTCCTTGGAAAGGAG[G/T]CTAAAGATATGTGTC | 90025 |
rs293529 | snp | A/T | 0.431473 | 0.171952 | intron-variant | UBE3D | GRCh38.p7 | 6:82936692 | CAATTAGGGGCTTAA[A/T]GCAATTAGCATCAAC | 90025 |
rs293530 | snp | A/G | 0.207864 | 0.246424 | intron-variant, downstream-variant-500B, utr-variant-3-prime | UBE3D | GRCh38.p7 | 6:82955460 | AGCTGAAAAACAATA[A/G]TTTTATATTTCACTC | 90025 |
rs293531 | snp | C/T | 0.442385 | 0.15965 | intron-variant | UBE3D | GRCh38.p7 | 6:82957217 | TTTGAAACTAGGGAA[C/T]TCCACGGGCTATCTC | 90025 |
rs293532 | snp | G/T | 0.44252 | 0.159487 | intron-variant | UBE3D | GRCh38.p7 | 6:82957224 | CTAGGGAATTCCACG[G/T]GCTATCTCCTGTGAA | 90025 |
rs719639 | snp | G/T | 0.456568 | 0.140818 | intron-variant | UBE3D | GRCh38.p7 | 6:83024306 | CACTATGCCTGTGAT[G/T]TGACTAACTTTTATA | 90025 |
rs883479 | snp | A/G | 0.265727 | 0.249505 | intron-variant | UBE3D | GRCh38.p7 | 6:82958843 | GTAAGTGAAGTCCAA[A/G]GAAGTGGCCAAAGCA | 90025 |
rs913577 | snp | A/G | 0.431621 | 0.171796 | intron-variant | UBE3D | GRCh38.p7 | 6:82935343 | tgtttgggtcacagg[A/G]gtgtatctctcatga | 90025 |
rs942899 | snp | C/G | 0.318896 | 0.240319 | intron-variant | UBE3D | GRCh38.p7 | 6:83053669 | ACAAATTAACCTTTT[C/G]TCAATGATTAGGTTA | 90025 |
rs950422 | snp | C/G | 0.422315 | 0.181128 | intron-variant | UBE3D | GRCh38.p7 | 6:82994036 | AGTGTGTGTTATTTC[C/G]ATCATTTTTCTCCTT | 90025 |
rs950423 | snp | C/T | 0.113685 | 0.209567 | intron-variant | UBE3D | GRCh38.p7 | 6:82994106 | AAAAATAAACACATG[C/T]ATACATAGAAGTTTA | 90025 |
rs950424 | snp | A/G | 0.112983 | 0.209108 | intron-variant | UBE3D | GRCh38.p7 | 6:82994101 | TAAACACATGCATAC[A/G]TAGAAGTTTATTTTA | 90025 |
rs950425 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | UBE3D | GRCh38.p7 | 6:82994249 | TGTAAGTAGGGGATT[A/G]ATATATAAATTGGTG | 90025 |
rs981983 | snp | A/G | 0.333491 | 0.235646 | intron-variant | UBE3D | GRCh38.p7 | 6:82905545 | CAATACTGAAATTAG[A/G]CCAATTAATACCCTA | 90025 |
rs981984 | snp | A/G | 0.333491 | 0.235646 | intron-variant | UBE3D | GRCh38.p7 | 6:82905688 | CACTGCAACATACCA[A/G]CAAACAAGGCCCGCA | 90025 |
rs982227 | snp | A/G | 0.1638 | 0.234669 | intron-variant | UBE3D | GRCh38.p7 | 6:82932170 | taggtaatttataaa[A/G]aaaagaggtttaatt | 90025 |
rs989226 | snp | A/G | 0.186737 | 0.241863 | intron-variant | UBE3D | GRCh38.p7 | 6:82894325 | CAAGATATGATAGCA[A/G]TGTTCCTTCAGTTGG | 90025 |
rs1016886 | snp | A/T | 0.421368 | 0.182025 | intron-variant | UBE3D | GRCh38.p7 | 6:82989726 | AGGGAACTGTCCCAT[A/T]TGCCCATGTTAAGTT | 90025 |
rs1124630 | snp | A/G | 0.421209 | 0.182174 | intron-variant | UBE3D | GRCh38.p7 | 6:82985320 | gtactaaaagaaaat[A/G]tggatgaattctcca | 90025 |
rs1416220 | snp | C/T | 0.147321 | 0.227941 | intron-variant | UBE3D | GRCh38.p7 | 6:83003557 | aaaattgcctaataa[C/T]gcatttctcaggatg | 90025 |
rs1538356 | snp | C/T | 0.448066 | 0.152544 | intron-variant | UBE3D | GRCh38.p7 | 6:83060189 | CTGCTTGGACCCtgt[C/T]atggactgaatgttt | 90025 |
rs1538357 | snp | A/G | 0.104548 | 0.203484 | intron-variant | UBE3D | GRCh38.p7 | 6:83060088 | gaggtagttagattt[A/G]gatgagttcttgagg | 90025 |
rs1556847 | snp | A/T | | | intron-variant | UBE3D | GRCh38.p7 | 6:82968196 | TACAAAAACTTGATT[A/T]CATTAAAATTAAGAA | 90025 |
rs1556848 | snp | C/T | 0.319856 | 0.240042 | intron-variant | UBE3D | GRCh38.p7 | 6:83045524 | TAAGAGTATTAGCCT[C/T]ATGCTTATTAATCTG | 90025 |
rs1778814 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBE3D | GRCh38.p7 | 6:82954315 | CTTATAATTGCATTA[C/G]AAATAGTAAGGTACT | 90025 |
rs1807008 | snp | C/G | 0 | 0 | intron-variant | UBE3D | GRCh38.p7 | 6:83052964 | ATGTCTTACATAAGT[C/G]CACTTTCCTCCATCC | 90025 |
rs1925780 | snp | A/C | | | intron-variant | UBE3D | GRCh38.p7 | 6:83041504 | aaaaaatgtagccac[A/C]ccgttatcacacctg | 90025 |
rs1932223 | snp | A/G | 0.140919 | 0.224948 | intron-variant | UBE3D | GRCh38.p7 | 6:82926001 | GGATATTTTTTAATA[A/G]GATTTTAGACTATAG | 90025 |
rs1960429 | snp | A/G | 0.127599 | 0.217986 | intron-variant | UBE3D | GRCh38.p7 | 6:82946016 | TGCCCCTTGAAGGCT[A/G]TTTTCTAGATCTTGT | 90025 |
rs1981129 | snp | C/T | 0.275464 | 0.2487 | intron-variant | UBE3D | GRCh38.p7 | 6:82899171 | GGCACACACTTGATC[C/T]CCCTAGGATGCTGGC | 90025 |
rs1981189 | snp | A/G | 0.297382 | 0.245469 | intron-variant | UBE3D | GRCh38.p7 | 6:83036818 | tgagcccaggggttc[A/G]aggctgtggtgcact | 90025 |
rs1981190 | snp | A/G | 0.320335 | 0.239902 | intron-variant | UBE3D | GRCh38.p7 | 6:83036810 | ggggttcaaggctgt[A/G]gtgcactattattgc | 90025 |
rs2015720 | snp | A/T | 0.153997 | 0.230832 | intron-variant | UBE3D | GRCh38.p7 | 6:83060458 | gcatttacaaccatc[A/T]atattactgtatcta | 90025 |
rs2027282 | snp | C/T | 0.31014 | 0.242659 | intron-variant | UBE3D | GRCh38.p7 | 6:83044762 | TCATTAACCACAAGG[C/T]TTGCAATGCTAATTT | 90025 |
rs2027580 | snp | A/T | 0.0770498 | 0.180522 | intron-variant | UBE3D | GRCh38.p7 | 6:83053558 | TAGGGACTGTAAAAA[A/T]ACCCAAAAACAACAA | 90025 |
rs2148013 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | DOPEY1, UBE3D | GRCh38.p7 | 6:83067697 | CGGGAGCCGAAGGGC[C/G]TAGTGACAGCTCCCA | 90025 |
rs2149533 | snp | A/G | 0.046775 | 0.145601 | intron-variant | UBE3D | GRCh38.p7 | 6:82972678 | CCAAGCTATATTTTT[A/G]TGTACATTTAAATTT | 90025 |