SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1030889 | snp | G/T | 0.26078 | 0.249767 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445608 | CTGGGTGGACTTTCA[G/T]GGGAAGCACATGGAG | 84993 |
rs2289187 | snp | A/G | 0.467845 | 0.122652 | intron-variant | UBL7 | GRCh38.p7 | 15:74452058 | GCCCGTATGGTGACA[A/G]CCAAAAGATCCTCAT | 84993 |
rs2289188 | snp | C/T | 0.482309 | 0.0923707 | intron-variant | UBL7 | GRCh38.p7 | 15:74450127 | ACCCAGAACTCCTGT[C/T]ATGGCTGAGGGTGCT | 84993 |
rs2304554 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBL7 | GRCh38.p7 | 15:74451349 | TAAAGAGACTTGGAC[C/T]ATCTTTTGAAGAATG | 84993 |
rs2415243 | snp | A/G | 0.439363 | 0.163222 | intron-variant | UBL7 | GRCh38.p7 | 15:74454430 | gcctgggcaacaaga[A/G]cgaaactctgtctca | 84993 |
rs4372642 | snp | A/T | 0.494358 | 0.0528145 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460095 | ataatagaaaaaatt[A/T]gcagggcgtggtggc | 84993 |
rs4468560 | snp | A/C | 0.482534 | 0.0918038 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460012 | tttgggaggccgcgg[A/C]ggacggatcacttaa | 84993 |
rs5813762 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462455 | CATGATTTTTTTTTT[-/T]ACTCTTAATGGTATT | 84993 |
rs6495101 | snp | A/T | 0.482534 | 0.0918038 | intron-variant | UBL7 | GRCh38.p7 | 15:74450411 | CAGGCAACCCTGGAC[A/T]GGTCCCTTCTCTTCC | 84993 |
rs7163775 | snp | A/G | 0.469544 | 0.119585 | intron-variant | UBL7 | GRCh38.p7 | 15:74452760 | ACCTCTTGCCCAGCC[A/G]GAATGCAGTGGCGCA | 84993 |
rs7166701 | snp | A/G | 0.365237 | 0.221857 | intron-variant | UBL7 | GRCh38.p7 | 15:74456674 | CAGTAGATCAGATCT[A/G]AAAAAAGAACTGTCC | 84993 |
rs7169985 | snp | C/G | 0.482384 | 0.0921818 | intron-variant | UBL7 | GRCh38.p7 | 15:74453437 | CACAAAGGCAGACAG[C/G]CACCACTGAGAGGGA | 84993 |
rs7175503 | snp | C/T | 0 | 0 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445661 | CGGAAGCATAAGCCT[C/T]TTCTGGGCACAGCTG | 84993 |
rs7497739 | snp | C/T | 0 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74446494 | TTCACTGTCTGAATT[C/T]CAAGAGGCTAAATTA | 84993 |
rs8037211 | snp | A/T | 0.482384 | 0.0921818 | intron-variant | UBL7 | GRCh38.p7 | 15:74455061 | gtacaattgttcatg[A/T]tccccaaaaggattc | 84993 |
rs8041946 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | UBL7 | GRCh38.p7 | 15:74455262 | GATGTCAACCTGCCA[C/G]TGTAACAAAGCTAAT | 84993 |
rs11544679 | snp | C/T | | | synonymous-codon | UBL7 | GRCh38.p7 | 15:74458721 | GCAGCTTATTGCTGG[C/T]AAACTCCAGGAGTCT | 84993 |
rs11544680 | snp | C/T | | | synonymous-codon | UBL7 | GRCh38.p7 | 15:74456595 | ACCTGGGTCCACTGT[C/T]CATGTTCTGCGAAAG | 84993 |
rs11852291 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | UBL7 | GRCh38.p7 | 15:74457624 | GGCCTGTAATCCCAG[C/T]TATTCAGGAGGCTGA | 84993 |
rs11853002 | snp | A/G | 0.0195117 | 0.0968254 | intron-variant | UBL7 | GRCh38.p7 | 15:74449701 | ACGAACAGATTTCAG[A/G]AGGAAGAACAGAAAG | 84993 |
rs11854461 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | UBL7 | GRCh38.p7 | 15:74447400 | CTAGGGTGACCTTTC[C/T]CCTCCTTAAAGCCTC | 84993 |
rs12440645 | snp | C/T | 0.467946 | 0.122472 | intron-variant | UBL7 | GRCh38.p7 | 15:74452920 | TTTCACCATATTGGT[C/T]AGGCTGGTCTCAAAC | 84993 |
rs12440654 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | UBL7 | GRCh38.p7 | 15:74453008 | tgagccaccgtgccc[A/G]gccCTGGGTCACACT | 84993 |
rs12594826 | snp | C/T | 0.084364 | 0.187256 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460232 | gggcgacagagactc[C/T]gtcccTCCCTGCCCC | 84993 |
rs28418795 | snp | G/T | 0 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74459241 | ACAGCTTTATAACAA[G/T]TTCCCTGCCTCTTGC | 84993 |
rs28494489 | snp | C/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74452943 | TCTCAAACTCCTGAC[C/G]TCAAGTGATCCACAC | 84993 |
rs28676598 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74453227 | TTACCTAATTTATTC[A/G]TTCAACAAACATGTA | 84993 |
rs34349059 | in-del | -/A | | | upstream-variant-2KB, nc-transcript-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461885 | TTTTTTGCACAGAAA[-/A]TTAGGATTACCGAAA | 84993 |
rs34517552 | in-del | -/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74449785 | CATCTCTCCCCTCGG[-/G]AAAATTACAGGACAG | 84993 |
rs34649295 | in-del | -/G | | | utr-variant-5-prime, intron-variant | UBL7 | GRCh38.p7 | 15:74459025 | GGGCGTACCATCAGG[-/G]AGGCCAGAACTAGAA | 84993 |
rs34947984 | in-del | -/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74454415 | GGACTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 84993 |
rs35032603 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461084 | ACATCGAGCCCGCGC[C/T]GCCCAGGGCCCCAGC | 84993 |
rs35240050 | in-del | -/C | | | intron-variant | UBL7 | GRCh38.p7 | 15:74450530 | TTGCCAGCTTAAAAT[-/C]CCTTGAAAAGCTCCC | 84993 |
rs35564796 | snp | C/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74455956 | GGTGAAACCCCGTCT[C/T]TACTAAAAAACACAA | 84993 |
rs35794633 | in-del | -/A | | | intron-variant | UBL7 | GRCh38.p7 | 15:74457845 | GGAAAAACAACAAAA[-/A]TAGGATGAACCCAAT | 84993 |
rs35947306 | in-del | -/C | | | intron-variant | UBL7 | GRCh38.p7 | 15:74455671 | TAGACACAAACTCCC[-/C]TGTCCCATTAGGAAA | 84993 |
rs35980770 | in-del | -/T | 0.482757 | 0.0912364 | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74463084 | GTCAATTTTTGACTC[-/T]TATTCTGTGCCATGG | 84993 |
rs55846825 | in-del | -/AAAAA | | | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459956 | AAAAAAAAAAAAAAA[-/AAAAA]GCCAGACGCGGTGGC | 84993 |
rs56253831 | snp | A/C | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460406 | ACATGTAAGTACACA[A/C]TCATAACAAAGCTCT | 84993 |
rs56924730 | snp | C/T | | | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445892 | CCTGCTTTGATGCCA[C/T]AGCATCAAGACCAGC | 84993 |
rs57283440 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | UBL7 | GRCh38.p7 | 15:74447840 | CTCTGGCCCCATCTG[C/T]GGATCTTCTACACTG | 84993 |
rs58398578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBL7 | GRCh38.p7 | 15:74451630 | CTTGCATGTACATCA[C/T]CACAATGGAACAATA | 84993 |
rs60629046 | snp | A/G | 0.00953236 | 0.0683763 | intron-variant | UBL7 | GRCh38.p7 | 15:74448645 | CTCAGCGCCATCTCA[A/G]TCTTATAGCAGATGC | 84993 |
rs61137560 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459318 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 84993 |
rs61143329 | snp | A/G | 0.0637235 | 0.166737 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459370 | CAGCGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 84993 |
rs61184870 | snp | A/C/G/T | 0.00342893 | 0.0412852 | intron-variant | UBL7 | GRCh38.p7 | 15:74449587 | CAGCACCATCTCCCC[A/C/G/T]ACATGTCAGCATGTC | 84993 |
rs62005799 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74451727 | TTAAAAAAAAAAAAG[A/G]CAAGACCACAGTAAA | 84993 |
rs62005800 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74457759 | AAAAAAAAAAAAAAG[A/G]ATTCACACAGAATCT | 84993 |
rs71137388 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459490 | TTTTTTTTTTTTTTT[-/T]GTACTTTTAGTAGAG | 84993 |
rs71399786 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459630 | CCACAACCCATCATT[C/T]TAAAACACAGATCTG | 84993 |
rs71399787 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459655 | GATCTGACCAAGTCA[C/T]TTCTCTGCTTAGAAC | 84993 |
rs71399788 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459658 | CTGACCAAGTCACTT[C/T]TCTGCTTAGAACTCT | 84993 |
rs71399789 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459660 | GACCAAGTCACTTCT[C/T]TGCTTAGAACTCTTC | 84993 |
rs71399790 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74459838 | GGCGTGGTAGTGCGC[A/C]CCTGTAGTGCCACCT | 84993 |
rs72728874 | snp | C/G | 0.00358779 | 0.0422022 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445570 | AGCCATTGAGAGAGA[C/G]AGAAATGTGGAAGGC | 84993 |
rs74025809 | snp | C/T | 0.0726307 | 0.176182 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445632 | CACCCAGCCACTCCA[C/T]AGACTGGACATCTCG | 84993 |
rs74025810 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | UBL7 | GRCh38.p7 | 15:74455072 | CATGATCCCCAAAAG[A/G]ATTCCAGGGCCTGGC | 84993 |
rs74025811 | snp | A/G | 0.0597382 | 0.162174 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460771 | CATTATTGCTTCCAA[A/G]GAGACCTCTGATAGA | 84993 |
rs74565454 | snp | A/G | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456128 | TGAGACTCCGTCTCA[A/G]AAAAAAAAAAAAAAA | 84993 |
rs74903425 | snp | A/T | 0.468249 | 0.121932 | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462698 | AGTAGAGACGGGGTT[A/T]CACCACGTTGGCCAG | 84993 |
rs76063377 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBL7 | GRCh38.p7 | 15:74449469 | TCCCAGGTTCAGAAA[A/G]GAATCCAAAAGCAGA | 84993 |
rs76512205 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBL7 | GRCh38.p7 | 15:74448674 | GCTCGCTGTTGTCAT[A/G]TCACCTCACAGCACT | 84993 |
rs76590578 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462492 | ATTAGATAATTTAAT[C/T]TCATTTTAAAACTTT | 84993 |
rs77218660 | snp | G/T | 0.00131731 | 0.0256304 | intron-variant, missense, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460679 | ATACCTGGCATACAT[G/T]GAACCCCAGAAAATA | 84993 |
rs77655065 | snp | A/C | 0.468148 | 0.122112 | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462699 | GTAGAGACGGGGTTT[A/C]ACCACGTTGGCCAGG | 84993 |
rs77700222 | snp | A/C | 0.0637235 | 0.166737 | upstream-variant-2KB, nc-transcript-variant, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462060 | CTGAATTCCCACATT[A/C]CAATGTGCGACCTGG | 84993 |
rs77995831 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, nc-transcript-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461616 | GCCTCTTCTGTGCTC[C/T]TCGCCGCTGACTTCC | 84993 |
rs78054428 | snp | G/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74451896 | TCATATTTGTATATA[G/T]CGCTAAGTTCACAGC | 84993 |
rs78074764 | snp | A/G | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456129 | GAGACTCCGTCTCAG[A/G]AAAAAAAAAAAAAAA | 84993 |
rs78087925 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBL7 | GRCh38.p7 | 15:74455006 | TTTTTGTCTTAATCC[A/G]TAGTGGTCTCAGAGT | 84993 |
rs78112942 | snp | A/G | 0.00307754 | 0.0391062 | synonymous-codon | UBL7 | GRCh38.p7 | 15:74449991 | AGAGGAGTCAGTCCC[A/G]GGCATTGGGGCACTG | 84993 |
rs78534058 | snp | A/G | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74457757 | AAAAAAAAAAAAAAA[A/G]GGATTCACACAGAAT | 84993 |
rs78775591 | snp | A/G | 0.444444 | 0.157135 | intron-variant | UBL7 | GRCh38.p7 | 15:74448170 | CAGCATCTGGACTCA[A/G]GCCTAGTATACACAT | 84993 |
rs78955495 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74451895 | TTCATATTTGTATAT[A/G]TCGCTAAGTTCACAG | 84993 |
rs79106784 | snp | A/G | 0.175576 | 0.238665 | intron-variant | UBL7 | GRCh38.p7 | 15:74456183 | CATGCCTGTAATCCC[A/G]GCTACTCGGGAGGCT | 84993 |
rs79175150 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | UBL7 | GRCh38.p7 | 15:74455329 | TTTTAAAACACACAT[A/G]CAAAATTTAAATCAT | 84993 |
rs79494487 | snp | C/G/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74451897 | CATATTTGTATATAT[C/G/T]GCTAAGTTCACAGCT | 84993 |
rs79643959 | snp | G/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456827 | ACTTTTTTTTTTTTG[G/T]AAAACAGGGTCTTAC | 84993 |
rs80016709 | snp | A/T | 0.175576 | 0.238665 | intron-variant | UBL7 | GRCh38.p7 | 15:74457365 | CCTGGCCAAGATGGT[A/T]AACCTCGTCTCTACC | 84993 |
rs80266690 | snp | G/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456825 | ATACTTTTTTTTTTT[G/T]GGAAAACAGGGTCTT | 84993 |
rs80343857 | snp | C/T | 0.243061 | 0.249904 | intron-variant | UBL7 | GRCh38.p7 | 15:74458605 | ATCCCAAGCCCTTAC[C/T]TTACTCTTGTAATTC | 84993 |
rs111247659 | snp | C/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74458679 | CCCAGTCCAGAGAGA[C/T]TCACCAATCAGCTCA | 84993 |
rs111423714 | snp | A/G | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456470 | CTTTGTTCCACCCAG[A/G]CTTGTGCCTCAAGAA | 84993 |
rs111591708 | snp | C/G/T | 0 | 0 | splice-acceptor-variant | UBL7 | GRCh38.p7 | 15:74449354 | TGTGGACCTGGTGTT[C/G/T]TGGAGAAAGAAGACA | 84993 |
rs112536890 | snp | C/G | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74455893 | ACTTTGGGAGGCCGA[C/G]GCGGGCAGATCACAA | 84993 |
rs112604589 | snp | C/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74458538 | TATATGATTTGTGTT[C/T]CTATTTACCCAACAT | 84993 |
rs112717743 | snp | C/T | 0.401747 | 0.198678 | intron-variant | UBL7 | GRCh38.p7 | 15:74456954 | AGCTGGGACTACAGG[C/T]ACATGCCACCACACC | 84993 |
rs112744397 | snp | A/C/T | 0 | 0 | intron-variant, utr-variant-5-prime, splice-donor-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461035 | TCCGGTGGCGACCTC[A/C/T]CCGCTCCAGTGGGAC | 84993 |
rs113192902 | snp | C/T | 0.5 | 0 | missense | UBL7 | GRCh38.p7 | 15:74448494 | TGAAGGCTGGGCTGC[C/T]CAGAGGCCTGAAGGG | 84993 |
rs113289400 | snp | C/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74450549 | TGAAAAGCTCCCTAA[C/T]TTCTACCACACGAAA | 84993 |
rs113386961 | snp | C/T | 0.5 | 0 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445758 | CCAAACTCCAAAGCC[C/T]CAGAGAGTCTGGGGG | 84993 |
rs113476596 | snp | C/T | 0 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74453175 | CGACAGTCCTGATCA[C/T]GAGGCTGTCTTTTGA | 84993 |
rs113554114 | snp | C/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74452050 | GAAACAGTATGAGGA[C/T]CTTTTGGCTGTCACC | 84993 |
rs113624937 | snp | C/G/T | 0 | 0 | splice-donor-variant | UBL7 | GRCh38.p7 | 15:74449625 | CAGGCAGGCCACTTA[C/G/T]TGGGTGAAAGTCATC | 84993 |
rs113802669 | snp | A/G | | | utr-variant-3-prime | UBL7 | GRCh38.p7 | 15:74446007 | GGTATATTGGGGAAG[A/G]GAGAGATGGAGGCAC | 84993 |
rs113808217 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBL7 | GRCh38.p7 | 15:74455598 | ACGATAATAACAAAA[A/G]GATACAAAGTTTACT | 84993 |
rs113971019 | snp | C/T | 0.5 | 0 | intron-variant | UBL7 | GRCh38.p7 | 15:74456698 | ACTGTCCACTTATAT[C/T]TTGCTCCTCAAAACA | 84993 |
rs114297993 | snp | A/G | 0.00182336 | 0.0301389 | intron-variant | UBL7 | GRCh38.p7 | 15:74449151 | GCTTGTTCCTTGGGG[A/G]CCCAGCCTTGATCTT | 84993 |
rs115010190 | snp | G/T | 0.0248432 | 0.108648 | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445515 | ATCAAAAAATGCTTG[G/T]TGAGAATAGACTGGT | 84993 |
rs115171791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBL7 | GRCh38.p7 | 15:74449527 | AATGGCGTATGTCCA[A/T]CTCCCAGCCTTGGGA | 84993 |