SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15191 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10179520 | AACTCCCCCACGGAC[A/C]CCTTCAACCGGCAGA | 10277 |
rs1046277 | snp | C/T | 0.23031 | 0.249223 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10180036 | CCGCAGCGAAGCTGC[C/T]GTTCATGTGTTGGAG | 10277 |
rs1074461 | snp | A/G | 0.472896 | 0.113214 | intron-variant | UBE4B | GRCh38.p7 | 1:10143387 | TTTAGACTGAGCCTC[A/G]CTCTATTGCCCAGGC | 10277 |
rs1801442 | snp | C/G/T | 1.64749e-05 | 0.00287005 | missense, downstream-variant-500B, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10171204 | GTGGNCCCCAAGTGC[C/G/T]GTGACCTGAAAGTTG | 10277 |
rs1830501 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10136641 | CCTTAAACTTCTggc[C/G]gggcatggtggctca | 10277 |
rs1973936 | snp | C/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10137998 | ggagtgcagtggtac[C/G]atctcagctcggtgc | 10277 |
rs2004601 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | UBE4B | GRCh38.p7 | 1:10146302 | actaaaaatacaaaa[A/T]ttaactgggtgtggt | 10277 |
rs2038353 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE4B | GRCh38.p7 | 1:10169742 | GCATAAggccaagca[C/T]ggtggctcatgcctg | 10277 |
rs2180184 | snp | A/G | 0.453087 | 0.145793 | intron-variant | UBE4B | GRCh38.p7 | 1:10175888 | actgtactacatgcc[A/G]caaaatggtacactt | 10277 |
rs2273297 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10179741 | CATGAGAGGGAGGGA[C/T]TGGATGTCTGCAGGG | 10277 |
rs2273298 | snp | A/G | 0.323926 | 0.23882 | intron-variant | UBE4B | GRCh38.p7 | 1:10158319 | TTGGAAAGCAAGAAA[A/G]TACATATCCCTCAGT | 10277 |
rs2273299 | snp | C/T | 0.323534 | 0.238941 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10158381 | TACCGGAGCCACCAG[C/T]GAGTTTTATGACAAG | 10277 |
rs2273300 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | UBE4B | GRCh38.p7 | 1:10161343 | TCTGCCTCCACACAC[A/G]GGCAGAGCTGCTTTG | 10277 |
rs2295294 | snp | A/T | 0.486288 | 0.0816578 | intron-variant | UBE4B | GRCh38.p7 | 1:10130826 | AGGGTAAGTGTTCAG[A/T]AAACAAATCCAGAGG | 10277 |
rs3762290 | snp | C/T | 0.474091 | 0.11083 | intron-variant | UBE4B | GRCh38.p7 | 1:10117732 | CCTAAGTTCCTAGTA[C/T]TGTGCCTGGCACATG | 10277 |
rs3790487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE4B | GRCh38.p7 | 1:10169475 | TCCATGGCTCTTGCA[C/T]TGAAATCTGTTTATG | 10277 |
rs3818158 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | UBE4B | GRCh38.p7 | 1:10151782 | TCTCTGATGATTCAG[C/G]AGGAACTACTGAAAG | 10277 |
rs4265433 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE4B | GRCh38.p7 | 1:10065497 | ATTTCCCCACGCTGC[A/G]GGGGTAGTTTCGGCC | 10277 |
rs4333851 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | UBE4B | GRCh38.p7 | 1:10086121 | GGACTACAGGCGCCC[A/G]CCACCACGCCAGGCT | 10277 |
rs4360526 | snp | C/T | 0.448836 | 0.15154 | intron-variant | UBE4B | GRCh38.p7 | 1:10086128 | AGGCGCCCGCCACCA[C/T]GCCAGGCTAATTTTT | 10277 |
rs4388708 | snp | C/T | 0.102726 | 0.202016 | intron-variant | UBE4B | GRCh38.p7 | 1:10088487 | TTCAAGAAATTCTCC[C/T]GCCTCAGCCTCCTGA | 10277 |
rs4415569 | snp | C/T | 0.16028 | 0.233346 | intron-variant | UBE4B | GRCh38.p7 | 1:10134449 | CCCGGGAGGCGGAGG[C/T]TGTAGTGAGCGAGGA | 10277 |
rs4442371 | snp | C/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10056311 | AAGGGGAAACTGAGC[C/T]TAAGAGGAAGATTAA | 10277 |
rs4443893 | snp | A/T | 0.223591 | 0.248601 | intron-variant | UBE4B | GRCh38.p7 | 1:10054072 | ATATTAGATTTTTTT[A/T]AAAAAAAAAGACAGG | 10277 |
rs4500322 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10158023 | ATTTGAGGTGCCATA[A/G]AATTTCTGTAAATTA | 10277 |
rs4543799 | snp | A/G | 0.466124 | 0.127311 | intron-variant | UBE4B | GRCh38.p7 | 1:10114131 | GTAAAGATGTGAGAA[A/G]AATGGGGCTTATTAT | 10277 |
rs4846193 | snp | G/T | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10150258 | CGTGATTTTGATTGG[G/T]ATGAAATTTTAAAAG | 10277 |
rs4846195 | snp | C/T | 0.232359 | 0.249377 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181529 | AGATTCTTCCTCAGG[C/T]CGGGCCCGGTGGCTC | 10277 |
rs4846196 | snp | A/G | 0.499424 | 0.0169631 | downstream-variant-500B | UBE4B | GRCh38.p7 | 1:10181582 | gggaggctgaggcgg[A/G]tggatcacctgacgt | 10277 |
rs5772395 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10082633 | TATTAAGAAGGCGAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs5772396 | in-del | -/T | | | intron-variant | UBE4B | GRCh38.p7 | 1:10115165 | ACTTTAATACCATAC[-/T]TTTTTTTTTTTTTTT | 10277 |
rs6541075 | snp | A/T | 0.490175 | 0.0693959 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032712 | GAGTCGTCCCTCCCC[A/T]TGCCAGCCTACCTGG | 10277 |
rs6541076 | snp | C/G | 0.451856 | 0.147493 | intron-variant | UBE4B | GRCh38.p7 | 1:10040833 | ccatgttggcttggc[C/G]ggtctcaaactcttg | 10277 |
rs6541077 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE4B | GRCh38.p7 | 1:10084843 | GCTGGGATTACAAGC[A/G]CCCGCCACCATTCCT | 10277 |
rs6541078 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10138883 | ctattctgttaatgt[A/G]gttgaattatatcag | 10277 |
rs6541079 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | UBE4B | GRCh38.p7 | 1:10175629 | gcactccagcctggg[C/T]gacagagcgagactc | 10277 |
rs6541080 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | UBE4B | GRCh38.p7 | 1:10175981 | acccttaaagcagtc[A/G]ctgtctagaccccct | 10277 |
rs6657925 | snp | C/G | 0.0146672 | 0.084371 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10031232 | gtagctgggattaca[C/G]gtgcccgccaccacg | 10277 |
rs6659436 | snp | C/T | 0.257454 | 0.249889 | intron-variant | UBE4B | GRCh38.p7 | 1:10159144 | ATGAAATCTTAGTTC[C/T]TGAATGTTGGAAGGA | 10277 |
rs6664155 | snp | C/T | 0.154329 | 0.23097 | intron-variant | UBE4B | GRCh38.p7 | 1:10120411 | gcctgtaatcccagc[C/T]acctgggaggctgag | 10277 |
rs6665885 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | UBE4B | GRCh38.p7 | 1:10154661 | ctggccaaaatggtg[A/C]aaccccgtctctact | 10277 |
rs6667049 | snp | C/T | 0.462363 | 0.131916 | intron-variant | UBE4B | GRCh38.p7 | 1:10161789 | ATGGAAAGCACGTGC[C/T]GTGCCAGTACCAGTG | 10277 |
rs6669051 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | UBE4B | GRCh38.p7 | 1:10116843 | tgagactagaaccca[C/T]gtctggttactccta | 10277 |
rs6671289 | snp | A/G | 0.463774 | 0.129618 | intron-variant | UBE4B | GRCh38.p7 | 1:10135882 | TTATTTAACCTATCT[A/G]AAGTGAATTCTGGTG | 10277 |
rs6673887 | snp | C/T | 0.3748 | 0.216622 | intron-variant | UBE4B | GRCh38.p7 | 1:10133763 | aaaatatacaaaagt[C/T]aTctgggcatggtgg | 10277 |
rs6676280 | snp | A/G | 0.49334 | 0.057322 | intron-variant | UBE4B | GRCh38.p7 | 1:10092824 | taagagtgaaactct[A/G]tctcaaaaaaaaaaa | 10277 |
rs6677855 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10137426 | gagttctgaaccctg[A/G]atatttcactctgtt | 10277 |
rs6678222 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10098284 | taaatatcatctacc[A/G]tattgcatgttaaaa | 10277 |
rs6678519 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE4B | GRCh38.p7 | 1:10068419 | cagtggtgcgatctc[A/G]gctcactgtgacctc | 10277 |
rs6679112 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10067642 | ttttttttgagaccc[A/G]gctctcaccgggttg | 10277 |
rs6679221 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10067789 | ctggagtgcaatggc[A/G]tgatctcagctcact | 10277 |
rs6681003 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10040742 | cctgcctcagcctcc[C/T]gagtagctgggatta | 10277 |
rs6682295 | snp | A/G | 0.194902 | 0.243853 | intron-variant | UBE4B | GRCh38.p7 | 1:10179139 | CAGCCTGCCGTCCTC[A/G]CCACGGAGCCTGTGG | 10277 |
rs6685910 | snp | A/T | 0.376592 | 0.215579 | intron-variant | UBE4B | GRCh38.p7 | 1:10135912 | GATTCATAGCAAAAA[A/T]TATAATACTGTTGTT | 10277 |
rs6687550 | snp | C/T | 0.159292 | 0.232964 | intron-variant | UBE4B | GRCh38.p7 | 1:10137554 | gacataccccttctt[C/T]cctggactgtgaaaa | 10277 |
rs6688765 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | UBE4B | GRCh38.p7 | 1:10040786 | ccatgcctggctaat[G/T]tttttgtatttttat | 10277 |
rs6688779 | snp | A/G | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10136495 | cttaaaaaaaaaaaa[A/G]aaaaaaGATTGTGAT | 10277 |
rs6691957 | snp | A/T | 0.160609 | 0.233472 | intron-variant | UBE4B | GRCh38.p7 | 1:10136676 | tgtaatcccagcact[A/T]tgggaggccaaggag | 10277 |
rs6692491 | snp | A/G | 0.476833 | 0.105105 | intron-variant | UBE4B | GRCh38.p7 | 1:10167836 | cctcgtgattcgccc[A/G]ccttggcttcgcaaa | 10277 |
rs6693010 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE4B | GRCh38.p7 | 1:10079307 | gggattacaggcatg[C/T]gccaccacgcccggc | 10277 |
rs6693449 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | UBE4B | GRCh38.p7 | 1:10037614 | CCAGTCTGGAATGCA[A/G]TGGCATGATCTTGGC | 10277 |
rs6693686 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBE4B | GRCh38.p7 | 1:10067975 | ccttgtgatccgccc[A/G]cctcagcctcccaaa | 10277 |
rs6696978 | snp | A/G | 0.300169 | 0.244914 | intron-variant | UBE4B | GRCh38.p7 | 1:10149499 | ATTAACAGTGCAGAT[A/G]ATGTATTCCTTGAAA | 10277 |
rs6697968 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10079457 | gagccaccgcacccg[A/G]cctcaaaatttactt | 10277 |
rs6700518 | snp | A/T | 0.179105 | 0.239737 | intron-variant | UBE4B | GRCh38.p7 | 1:10150515 | TATAGTTAATATAAC[A/T]TGCTACAGCCAGTAA | 10277 |
rs6701103 | snp | A/G | 0.165853 | 0.235413 | intron-variant | UBE4B | GRCh38.p7 | 1:10080195 | gggaggccgagatgg[A/G]gggatcatgaggtca | 10277 |
rs6702986 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | UBE4B | GRCh38.p7 | 1:10090213 | cagcctcagcctcct[C/G]ggctcaggtgaccca | 10277 |
rs7354817 | snp | A/T | 0.486855 | 0.0799975 | intron-variant | UBE4B | GRCh38.p7 | 1:10175654 | agactccgtctcaaa[A/T]aaataaataaataaa | 10277 |
rs7355148 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | UBE4B | GRCh38.p7 | 1:10175909 | gtagtacagtcacag[C/T]gttgcacagccacca | 10277 |
rs7412246 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10163223 | agcatgtaccaccac[A/G]cttggctaattaaaa | 10277 |
rs7414561 | snp | A/G/T | 6.5895e-05 | 0.00573967 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10137107 | GCCGAAATTCCCTAC[A/G/T]GAGTGCTTCTTTCTC | 10277 |
rs7416007 | snp | A/G | 0 | 0 | intron-variant | UBE4B | GRCh38.p7 | 1:10125132 | ttgtgtctggaaaaa[A/G]gaaaaagaaaaagaa | 10277 |
rs7418410 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | UBE4B | GRCh38.p7 | 1:10176344 | acctgttttcagtta[C/T]tttgggtctacactt | 10277 |
rs7512714 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10131436 | gttgcagtgagccaa[G/T]atcacgccactgcac | 10277 |
rs7517298 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10032919 | GGCTGCCACGTCCCG[A/G]CGCCAGAAGCCCCGC | 10277 |
rs7522444 | snp | C/G/T | 0.128162 | 0.220096 | intron-variant | UBE4B | GRCh38.p7 | 1:10156332 | gcactcttgacctcc[C/G/T]gggctcaagtgatcc | 10277 |
rs7524177 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10060735 | GCTGTGTATTTTAGA[A/G]TCCCTAGTGAGCTAG | 10277 |
rs7528979 | snp | C/T | 0.494484 | 0.0522255 | utr-variant-5-prime, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10033399 | AGTGGCGCCTTAAGA[C/T]AACCCTGTAGCAGCA | 10277 |
rs7529458 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | UBE4B | GRCh38.p7 | 1:10061073 | TGTTTTCTGTTTTTT[C/T]TTTTATCTCAAAAGA | 10277 |
rs7531071 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE4B | GRCh38.p7 | 1:10134281 | tttgggaggccgaga[C/T]gggcgtatcacctga | 10277 |
rs7538285 | snp | A/G | 0.118933 | 0.212888 | intron-variant | UBE4B | GRCh38.p7 | 1:10074469 | tgcaccaaaaccttt[A/G]cagcagaacttccgg | 10277 |
rs7538883 | snp | A/G | 0.3752 | 0.216391 | intron-variant | UBE4B | GRCh38.p7 | 1:10135475 | TGGGCATGGTGGCAC[A/G]CGCCTGTAATCCCAG | 10277 |
rs7539725 | snp | A/G | 0.465683 | 0.126415 | intron-variant | UBE4B | GRCh38.p7 | 1:10065349 | AGTGGCGGGAGGAGC[A/G]TGCGGGGGAGGAAGG | 10277 |
rs7540431 | snp | A/G | 0.498852 | 0.0239341 | intron-variant | UBE4B | GRCh38.p7 | 1:10175454 | caggagatcgagacc[A/G]tcctggctaacacgg | 10277 |
rs7540888 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | UBE4B | GRCh38.p7 | 1:10102699 | tacaggtgtgagcca[C/G]cacgcccggccATCT | 10277 |
rs7541780 | snp | C/T | 0.3748 | 0.216622 | intron-variant | UBE4B | GRCh38.p7 | 1:10135548 | TCATGACCAGCCTGA[C/T]CACCATGGTGAAACC | 10277 |
rs7542626 | snp | A/C | | | intron-variant | UBE4B | GRCh38.p7 | 1:10066056 | ctccttccctccccc[A/C]ctccttccctctctc | 10277 |
rs7546283 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | UBE4B | GRCh38.p7 | 1:10097760 | ggttgctgtgacctg[A/G]gatcgcaccgctgca | 10277 |
rs7546642 | snp | A/G | 0.0879473 | 0.190365 | synonymous-codon, nc-transcript-variant | UBE4B | GRCh38.p7 | 1:10178712 | AGGGATCAAATCCAC[A/G]ATAGCAATAGAAAAA | 10277 |
rs7549318 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | UBE4B | GRCh38.p7 | 1:10175511 | aaaaaattagccagg[C/T]gtggtggcgggcgcc | 10277 |
rs7550904 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10049805 | tgagatgggagaatc[A/G]cttgagcccggcagg | 10277 |
rs7553655 | snp | A/G | 0.32627 | 0.238082 | intron-variant | UBE4B | GRCh38.p7 | 1:10175434 | aggcgggcggatcac[A/G]aggtcaggagatcga | 10277 |
rs7553668 | snp | A/G/T | 0.500158 | 0.0507834 | intron-variant | UBE4B | GRCh38.p7 | 1:10175479 | acacggtgaaacccc[A/G/T]tctctactaaaaata | 10277 |
rs7553760 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | UBE4B | GRCh38.p7 | 1:10175508 | tacaaaaaattagcc[A/G]ggcgtggtggcgggc | 10277 |
rs7555121 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10090200 | ttgtggctcactgca[A/G]cctcagcctcctggg | 10277 |
rs7556506 | snp | C/G/T | 0.291493 | 0.246533 | intron-variant | UBE4B | GRCh38.p7 | 1:10175462 | cgagaccgtcctggc[C/G/T]aacacggtgaaaccc | 10277 |
rs9430244 | snp | A/G | 0.257454 | 0.249889 | intron-variant, upstream-variant-2KB | UBE4B | GRCh38.p7 | 1:10095225 | AGTTTTAGGCATTAG[A/G]TGTAGCTCTGTTACT | 10277 |
rs9430245 | snp | A/T | 0.451608 | 0.147832 | intron-variant | UBE4B | GRCh38.p7 | 1:10097052 | TCAAAAAAAAAAAAA[A/T]AATAATAATAATAAT | 10277 |
rs9430246 | snp | A/G | | | intron-variant | UBE4B | GRCh38.p7 | 1:10173712 | CAGGGCTCTTCCATC[A/G]TTGCCGTAGAGAGAC | 10277 |
rs9662454 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE4B | GRCh38.p7 | 1:10136749 | acatggtgaaacctc[A/G]tctctcctaaaaatg | 10277 |