SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2781 | snp | C/G | 0.472052 | 0.11486 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921979 | CTGCTATTCCCAGAT[C/G]AAGATTTGGTGGAAG | 55833 |
rs11848 | snp | A/G | 0.0869089 | 0.189476 | utr-variant-3-prime | UBAP2 | GRCh38.p7 | 9:33921921 | CCTGTTTGTCTTCAT[A/G]TAGAACAGGGGCTTC | 55833 |
rs307642 | snp | A/G | 0.346368 | 0.23068 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930187 | TCCTATTACACCATG[A/G]CATCCTCAAAATGGT | 55833 |
rs307643 | snp | C/T | 0.345925 | 0.230864 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930791 | ctcctgcctcagtct[C/T]ctgagtagctggggt | 55833 |
rs307644 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | UBAP2 | GRCh38.p7 | 9:33930945 | CACGCAGTGCATACA[C/T]GTAGTCATTTCCCCA | 55833 |
rs307645 | snp | C/T | 0.467845 | 0.122652 | intron-variant | UBAP2 | GRCh38.p7 | 9:33931400 | AAAAAAACCTCCAGA[C/T]CATGTATTCCAGCCT | 55833 |
rs307646 | snp | A/G | 0.346147 | 0.230772 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932340 | ACAGATAAGGTCTGG[A/G]GCAATGATTCTTCCC | 55833 |
rs307647 | snp | G/T | 0.346147 | 0.230772 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932442 | TGCCATCAAGACATT[G/T]CAGCCAAGCAACTCT | 55833 |
rs307648 | snp | C/G | 0.467845 | 0.122652 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932690 | CCAGATGAACAAGAC[C/G]CACGTGGGTCAGTGA | 55833 |
rs307649 | snp | G/T | 0.343254 | 0.231956 | intron-variant | UBAP2 | GRCh38.p7 | 9:33932704 | CGCACGTGGGTCAGT[G/T]AGCTAGATTCAAACT | 55833 |
rs307650 | snp | A/G | 0.113685 | 0.209567 | intron-variant, utr-variant-5-prime, downstream-variant-500B | UBAP2, SNORD121B | GRCh38.p7 | 9:33934196 | ACTTCCAAATGCACA[A/G]TGAGCATTTCCTTGG | 55833 |
rs307651 | snp | G/T | 0.466412 | 0.125164 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935075 | GCCAGCTTGACTGAT[G/T]GTTTATAGTAGTTTT | 55833 |
rs307652 | snp | C/T | 0.465874 | 0.126089 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121B | GRCh38.p7 | 9:33935738 | AGTTGGTCAATGGCT[C/T]ATTCGTTAAAAAGCA | 55833 |
rs307653 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | UBAP2 | GRCh38.p7 | 9:33946739 | ATGAATGCGCCTAAA[C/T]CAGCTCTGCCATTTG | 55833 |
rs307654 | snp | C/T | 0.451234 | 0.14834 | intron-variant | UBAP2 | GRCh38.p7 | 9:33948654 | CAAGGCTTTAAAACA[C/T]ATCAAGTATTTTCAC | 55833 |
rs307655 | snp | A/G | 0.452842 | 0.146134 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949107 | TGATCTCTGCTCACT[A/G]CAAGCTCCGCCTCCT | 55833 |
rs307656 | snp | A/G | 0.450483 | 0.149354 | intron-variant | UBAP2 | GRCh38.p7 | 9:33949722 | CGTGTGTGCGCGTGC[A/G]TGCGCGCACACACAC | 55833 |
rs307657 | snp | C/G | 0.343924 | 0.231686 | intron-variant | UBAP2 | GRCh38.p7 | 9:33941455 | AGTGTGTGGATAGAT[C/G]TGCAGGTTCATACAC | 55833 |
rs307658 | snp | A/G | 0.468305 | 0.121832 | missense | UBAP2 | GRCh38.p7 | 9:33941761 | CAAGCTCATCACTGA[A/G]TTCTGCTAGTCCAGT | 55833 |
rs307659 | snp | A/G | 0.34303 | 0.232046 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942667 | gcttggctcgctgca[A/G]cctctgcctcccagg | 55833 |
rs307660 | snp | A/G | 0.458545 | 0.137872 | intron-variant | UBAP2 | GRCh38.p7 | 9:33942932 | tatcccaggagtaga[A/G]ttgctgagtcatatg | 55833 |
rs307661 | snp | A/C | 0.44638 | 0.154709 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960154 | GCCAGGAATATGAGA[A/C]CTGCCTGAGTAACAA | 55833 |
rs307662 | snp | C/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33960641 | AGATGTGCGCCACCA[C/T]GCCTGGCTAATTTTG | 55833 |
rs307663 | snp | A/C | 0.097727 | 0.198275 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961337 | AAAGGATGCTTCTCT[A/C]AATTTGATAATTCAG | 55833 |
rs307664 | snp | A/T | 0.451109 | 0.148509 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961354 | GAGCTAATATTTTAT[A/T]AAAAGGATGCTTCTC | 55833 |
rs307665 | snp | C/G | 0.114387 | 0.210022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33961508 | TCATCCATAACACAT[C/G]TAAGTACTTTCAAAA | 55833 |
rs307666 | snp | C/T | 0.114387 | 0.210022 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962187 | AGTACTTTAATATTT[C/T]TTATGTAGGTTTTTG | 55833 |
rs307667 | snp | C/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962503 | acacgccaccacgcc[C/T]ggctaatttttgtag | 55833 |
rs307668 | snp | C/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962864 | agcctcccaagtagc[C/T]gggatttacaggtgt | 55833 |
rs307669 | snp | C/T | 0.438806 | 0.163867 | intron-variant | UBAP2 | GRCh38.p7 | 9:33965975 | gcaggctctgcctcc[C/T]gggttcacgccattc | 55833 |
rs307670 | snp | A/G | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33966604 | agaccctcataaaag[A/G]gaacatattcagtgt | 55833 |
rs307671 | snp | C/T | 0.343254 | 0.231956 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968456 | TGAAGCTGAAGAAGC[C/T]GACCAGGCTGCACAT | 55833 |
rs307672 | snp | C/T | 0.030665 | 0.119967 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968558 | TGTTTCTGAGTGGCA[C/T]GTGGGATTTGAGCCT | 55833 |
rs307673 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | UBAP2 | GRCh38.p7 | 9:33968821 | ggtgagtgactacaa[A/G]tgagtatggagtttg | 55833 |
rs307674 | snp | A/G | 0.097727 | 0.198275 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969155 | atagcaacataattc[A/G]tcattataaaaaagt | 55833 |
rs307675 | snp | A/G | 0.458545 | 0.137872 | intron-variant | UBAP2 | GRCh38.p7 | 9:33969354 | ttgcattgttgtgga[A/G]gctggtcttaaactc | 55833 |
rs307676 | snp | C/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33970814 | cttcatctcaaacaa[C/T]gacaacaaaaacgaa | 55833 |
rs307677 | snp | C/G | 0.438806 | 0.163867 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971314 | CACCATTAGAAATGG[C/G]AAGTACTTCCAGTAA | 55833 |
rs307678 | snp | C/T | 0.343701 | 0.231776 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971443 | AAGGAATTTGATTTT[C/T]CCTTCTGCAAGCTAA | 55833 |
rs307679 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971489 | TGGTTCTTACCACCC[A/G]AAGTCTGTCACATAC | 55833 |
rs307680 | snp | C/T | 0.114036 | 0.209795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33971548 | TAGCCTGTTTTTCAT[C/T]CTTTTCCATCAGCAC | 55833 |
rs307681 | snp | A/G | 0.114738 | 0.210248 | intron-variant | UBAP2 | GRCh38.p7 | 9:33972036 | AGCAGACAAGGAGAC[A/G]TATAATCTTTCAAGG | 55833 |
rs307682 | snp | C/T | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973326 | ATAATGATAATATTG[C/T]CTGGGTAGTGAGTAT | 55833 |
rs307683 | snp | A/C | 0.466721 | 0.124627 | intron-variant | UBAP2 | GRCh38.p7 | 9:33973450 | GAAAAGAATTAAATT[A/C]TCCTTGTATTATATT | 55833 |
rs307684 | snp | C/T | 0.439502 | 0.163061 | intron-variant | UBAP2 | GRCh38.p7 | 9:33974894 | acagttcctaacttg[C/T]gtcactgttctccag | 55833 |
rs307685 | snp | G/T | 0.438666 | 0.164028 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975398 | gtcacccaggctgga[G/T]tgcagtggcacgatc | 55833 |
rs307686 | snp | A/G | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33975529 | ttacaggcatgagcc[A/G]ctgcacctggcccca | 55833 |
rs307687 | snp | G/T | 0.114036 | 0.209795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929687 | TTCTTGGTTCCTTTT[G/T]TTGTCAGGTCTTTGG | 55833 |
rs307688 | snp | C/T | 0.46845 | 0.121572 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929512 | ACATAAAGGAAATCT[C/T]AGCATCTTCTCCTGC | 55833 |
rs307689 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | UBAP2 | GRCh38.p7 | 9:33929022 | ACATGGTTTCCTGGG[A/G]CTCCAAGGCGTCTTG | 55833 |
rs307690 | snp | C/T | 0.114036 | 0.209795 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928428 | CCACAGGAAGCCCAG[C/T]GTAAGTCTCAATCTT | 55833 |
rs307691 | snp | C/T | 0.364817 | 0.222075 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928225 | TGAACATCAAAACTA[C/T]TAACATTAAGCTTTA | 55833 |
rs307692 | snp | C/T | 0.00161325 | 0.0283553 | missense, utr-variant-5-prime | UBAP2 | GRCh38.p7 | 9:33927901 | CCGCATCCTCAGGCG[C/T]CAGCCTGTCCAGTAG | 55833 |
rs307693 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926451 | TAAAGCTATGGTCAC[A/G]CCTGGCACAACCGCC | 55833 |
rs307694 | snp | A/T | 0.471196 | 0.1165 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925370 | GTTCCTGCCTGGAGA[A/T]TTCTCGTGTTCTGTG | 55833 |
rs307695 | snp | A/C | 0.115088 | 0.210473 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925314 | TCTGCTCCCGTCCTC[A/C]GTTGTGCAGCTCTGT | 55833 |
rs307696 | snp | A/C | 0.355096 | 0.226837 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925212 | GAGTGCCATTCCCAG[A/C]CAGGATGGCTCCTTT | 55833 |
rs307697 | snp | A/G | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982589 | TATAATTTTCTCATC[A/G]GTATATATACCGGTG | 55833 |
rs307698 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | UBAP2 | GRCh38.p7 | 9:33982881 | aacaaaaaaaaaaaa[A/C]caaaaaaaaaCACCA | 55833 |
rs307699 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983729 | AGATGGCAACGAAGA[A/G]TGTTGGCACGTACAC | 55833 |
rs307700 | snp | C/T | 0.438946 | 0.163706 | intron-variant | UBAP2 | GRCh38.p7 | 9:33983933 | cagagtgatgctctg[C/T]ctcaaataaaaaaaT | 55833 |
rs307701 | snp | A/T | 0.166653 | 0.235697 | intron-variant | UBAP2 | GRCh38.p7 | 9:33984508 | aaagaaaaaaaaaaa[A/T]tttttttttaagaga | 55833 |
rs307702 | snp | A/G | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985037 | atactgttttccaaa[A/G]tggctgtaccagttt | 55833 |
rs307703 | snp | C/G | 0.458315 | 0.13822 | intron-variant | UBAP2 | GRCh38.p7 | 9:33985467 | agtgatatatttaca[C/G]gttggaatactactc | 55833 |
rs544169 | snp | C/T | 0.438806 | 0.163867 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956793 | TGTTAGCATTGTTGG[C/T]GGGTTTATTGGTATT | 55833 |
rs553963 | snp | A/G | 0.452473 | 0.146644 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33954269 | TGTGTGTGTGTGTGT[A/G]TATACACACACTTAA | 55833 |
rs558415 | snp | A/G | 0.114387 | 0.210022 | intron-variant, upstream-variant-2KB | UBAP2, SNORD121A | GRCh38.p7 | 9:33953772 | TGAGAAAATTGTTTA[A/G]TTTTACTTTATTGCT | 55833 |
rs573563 | snp | C/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978597 | GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 55833 |
rs576286 | snp | C/T | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978303 | CAAGTGATCCTCCCA[C/T]CTTGACCTACCAAGG | 55833 |
rs595556 | snp | C/G | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:33951954 | AAATAGAGAAGCCTT[C/G]GGCTGTTCTACTTCA | 55833 |
rs633706 | snp | A/C | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978717 | TCTCGGCTCATTGCA[A/C]GCTCCCCCTCCTGGG | 55833 |
rs634110 | snp | G/T | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:33978637 | ACCCGCCAGCACATC[G/T]GGCTAATTTTTTGTA | 55833 |
rs636339 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAP2 | GRCh38.p7 | 9:33956391 | gcacagattgcagtg[A/G]gccgagatcacgtca | 55833 |
rs668071 | snp | A/C | 0.438806 | 0.163867 | intron-variant | UBAP2 | GRCh38.p7 | 9:33957504 | TAAATGAAATCATAA[A/C]AGTATCCAAACCTTT | 55833 |
rs733105 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBAP2 | GRCh38.p7 | 9:33928084 | CCTGCCTGCTCAGCC[G/T]TGAGACTTGGGCCCA | 55833 |
rs745532 | snp | A/G | 0.469148 | 0.120308 | intron-variant | UBAP2 | GRCh38.p7 | 9:33927327 | AGCCCCTTTCCCCCA[A/G]TCCCTAAGGTCCCAC | 55833 |
rs747091 | snp | A/C | 0.476314 | 0.106217 | intron-variant | UBAP2 | GRCh38.p7 | 9:34045016 | TTTCCATTTTTTGAT[A/C]ACTAATTTTCATGCT | 55833 |
rs834027 | snp | A/G | 0.466824 | 0.124448 | intron-variant | UBAP2 | GRCh38.p7 | 9:33988237 | ACAGCAATGAATAAA[A/G]TAAGTAAAATCTTTG | 55833 |
rs834028 | snp | C/T | 0.097727 | 0.198275 | intron-variant | UBAP2 | GRCh38.p7 | 9:33986178 | gtagtcccagctact[C/T]gagaggctaaggcag | 55833 |
rs834029 | snp | A/G | 0.438666 | 0.164028 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976717 | GAGCCACTGCTCCCA[A/G]CCTAAGAAAGAAAAT | 55833 |
rs844305 | snp | G/T | 0.459914 | 0.13578 | intron-variant | UBAP2 | GRCh38.p7 | 9:33976579 | aacattttccacacc[G/T]cagaagtatacctta | 55833 |
rs874572 | snp | C/T | 0.232651 | 0.249397 | intron-variant | UBAP2 | GRCh38.p7 | 9:33933707 | ACATGTCACAAGATA[C/T]TGAGCATATTTTCAG | 55833 |
rs914604 | snp | G/T | 0.119978 | 0.213528 | intron-variant | UBAP2 | GRCh38.p7 | 9:33926498 | CTCAGTAGTGGTGCT[G/T]AGAGGTTCCTCAGGC | 55833 |
rs927719 | snp | C/T | 0 | 0 | intron-variant | UBAP2 | GRCh38.p7 | 9:33925769 | CAGTGATGCCTTCTT[C/T]CCCGTGGGTGTTGCT | 55833 |
rs932969 | snp | A/G | 0.232651 | 0.249397 | intron-variant | UBAP2 | GRCh38.p7 | 9:34001457 | TGTGACTCTAAGTCT[A/G]GTTTTACCAACCGTG | 55833 |
rs1149545 | snp | C/T | | | intron-variant | UBAP2 | GRCh38.p7 | 9:34038323 | ccccacggtctccct[C/T]tgatgccaagccaaa | 55833 |
rs1543604 | snp | G/T | 0.413083 | 0.189483 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040799 | TCATTCTAGGTGTCT[G/T]GAAAAAGTTCAGCTT | 55833 |
rs1543605 | snp | C/G | 0.438946 | 0.163706 | intron-variant | UBAP2 | GRCh38.p7 | 9:34040776 | TTCAGCTTATACACA[C/G]AGTGGATGCCCTAAG | 55833 |
rs1628620 | snp | A/G | 0.114036 | 0.209795 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025878 | AAAAACAGCAGTTAA[A/G]CCGGGCATGGTAGCT | 55833 |
rs1629188 | snp | C/G | 0.438946 | 0.163706 | intron-variant | UBAP2 | GRCh38.p7 | 9:34036531 | TCCAGGGTACTGCTG[C/G]CTGTGACAGAGAAAA | 55833 |
rs1631398 | snp | A/G | 0.466824 | 0.124448 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023112 | GCGCCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG | 55833 |
rs1632692 | snp | A/T | 0.454904 | 0.143228 | intron-variant | UBAP2 | GRCh38.p7 | 9:33962680 | TAAATAAATAAATAA[A/T]TAATTAAAAAATAGG | 55833 |
rs1758629 | snp | A/G | 0.431029 | 0.17242 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033505 | TTATTTTTGTACTCA[A/G]TAACCATCCCTACCT | 55833 |
rs1758630 | snp | A/G | 0.343477 | 0.231866 | intron-variant | UBAP2 | GRCh38.p7 | 9:34023777 | CAGGCCGGGTGCAGT[A/G]GCTCACGCCTGTAAT | 55833 |
rs1758631 | snp | G/T | 0.439224 | 0.163383 | intron-variant | UBAP2 | GRCh38.p7 | 9:34024958 | CACTACACTCCAATC[G/T]GGGCGACAGAACAAG | 55833 |
rs1758632 | snp | C/G | 0.466618 | 0.124806 | intron-variant | UBAP2 | GRCh38.p7 | 9:34025642 | ATGAGGAAAGAAAGT[C/G]TCCGGCCGAATAAAC | 55833 |
rs1758633 | snp | C/G | 0.438946 | 0.163706 | intron-variant | UBAP2 | GRCh38.p7 | 9:34027925 | CAGAACAGCCACCAA[C/G]ACAAAGTCTACACCC | 55833 |
rs1760815 | snp | C/T | 0.466824 | 0.124448 | intron-variant | UBAP2 | GRCh38.p7 | 9:34041929 | caagcgattctcctt[C/T]ctcagcctcccaaat | 55833 |
rs1760816 | snp | A/T | 0.466824 | 0.124448 | intron-variant | UBAP2 | GRCh38.p7 | 9:34034927 | TGTTTTTGAGAGTAA[A/T]CCGGATGTAGAGAAC | 55833 |
rs1760817 | snp | C/T | 0.11228 | 0.208646 | intron-variant | UBAP2 | GRCh38.p7 | 9:34033885 | agccaggcatggtgg[C/T]gggtgcctgtaatcc | 55833 |