SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs776541746 | snp | C/G | 1.65523e-05 | 0.00287678 | missense | UBL7 | GRCh38.p7 | 15:74458699 | CAATCAGCTCAGGGT[C/G]TGGAACAGACTCCTG | 84993 |
rs776631456 | snp | A/T | 1.65531e-05 | 0.00287686 | missense | UBL7 | GRCh38.p7 | 15:74458816 | GAATAGACTTTGGAG[A/T]AAGTGGCTGGTCAGC | 84993 |
rs776633925 | snp | C/G/T | 4.97173e-05 | 0.00498564 | intron-variant | UBL7 | GRCh38.p7 | 15:74449687 | CCACCTGGAGGAGGA[C/G/T]GAACAGATTTCAGGA | 84993 |
rs776746821 | snp | C/T | 1.65176e-05 | 0.00287376 | missense | UBL7 | GRCh38.p7 | 15:74446175 | CGCAGGCTCAGCTCA[C/T]CGTCCTGGATGCCCA | 84993 |
rs776844462 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74452989 | AGTGCTAGGATTACA[A/G]GCGTGAGCCACCGTG | 84993 |
rs777060082 | snp | A/G | 3.56125e-05 | 0.0042196 | missense | UBL7 | GRCh38.p7 | 15:74449223 | TGAGAGCTGCTCTCC[A/G]GAGTGCTGGCCAGGG | 84993 |
rs777146598 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74452786 | GCGCAATCTCGGCTC[A/G]CTGCAACCTCCACCT | 84993 |
rs777343468 | in-del | -/CTCT | 3.34983e-05 | 0.00409244 | utr-variant-5-prime, frameshift-variant | UBL7 | GRCh38.p7 | 15:74458883 | CCTCTCTCTTTCGCG[-/CTCT]CTCTTTCTCCCTGTA | 84993 |
rs777479880 | snp | C/T | 1.71185e-05 | 0.00292557 | intron-variant | UBL7 | GRCh38.p7 | 15:74458919 | AGAACAAAACCTCAG[C/T]GGTTAAAAGACAGAC | 84993 |
rs777629498 | snp | C/T | 3.29712e-05 | 0.00406011 | intron-variant | UBL7 | GRCh38.p7 | 15:74451404 | TCCTTTTCCGACAAC[C/T]CCTATTTCCTCAAAT | 84993 |
rs777765289 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461282 | TTGCAAAGCTTCCGG[G/T]TCTGGGGGAAGGCGT | 84993 |
rs777787494 | snp | C/T | 3.33784e-05 | 0.0040851 | synonymous-codon | UBL7 | GRCh38.p7 | 15:74449300 | AGCTCCACTGTACCC[C/T]AGGGAGGCTGGGCGG | 84993 |
rs777969143 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462466 | ATGATTTTTTTTTTA[C/T]TCTTAATGGTATTAG | 84993 |
rs777984712 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462972 | GATTCATCTCTTCCA[C/T]ATGGGTGTACAATTG | 84993 |
rs778056476 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | UBL7 | GRCh38.p7 | 15:74456633 | CATAGAAGTCAAGTG[C/T]CTGGTCATCTTTTAG | 84993 |
rs778077082 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | UBL7 | GRCh38.p7 | 15:74449608 | TCAGCATGTCAGGCA[A/G]GCAGGCAGGCCACTT | 84993 |
rs778167414 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | UBL7 | GRCh38.p7 | 15:74456545 | CTAAGGGCTGCCCCT[C/T]ACTCACCCGGTTTCT | 84993 |
rs778179790 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461869 | TAAAATGGAACAGAA[A/T]TTTTTTTGCACAGAA | 84993 |
rs778193993 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74455118 | AACCTCTGGATGTCA[A/G]GAACTCTGTTCCTCT | 84993 |
rs778287851 | snp | C/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74449124 | AAGGCAAATCTACTC[C/T]ACTGCTGGGGAGCTT | 84993 |
rs778331961 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74462505 | ATTTCATTTTAAAAC[-/T]TTTTTTTTTTTTTGA | 84993 |
rs778358692 | snp | A/G | 3.41227e-05 | 0.0041304 | intron-variant | UBL7 | GRCh38.p7 | 15:74458638 | GAAGTATCCTCCCCC[A/G]AAAGAGATCAGAGCA | 84993 |
rs778450980 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | UBL7 | GRCh38.p7 | 15:74446239 | GGCTCTGTGGAAAGA[C/T]AGGAATGGGCAGAAG | 84993 |
rs778561884 | snp | C/G | 1.65384e-05 | 0.00287557 | missense | UBL7 | GRCh38.p7 | 15:74446132 | CTCCAGGGCTGCTTG[C/G]ATGTCCCCACCGGTG | 84993 |
rs778738684 | snp | C/T | 4.94719e-05 | 0.00497328 | | | GRCh38.p7 | 15:74451397 | TGTTTTCTCCTTTTC[C/T]GACAACTCCTATTTC | 84993 |
rs778947349 | snp | A/C | 1.64817e-05 | 0.00287064 | intron-variant | UBL7 | GRCh38.p7 | 15:74456540 | CCTGCCTAAGGGCTG[A/C]CCCTCACTCACCCGG | 84993 |
rs779183433 | snp | A/G | 1.6708e-05 | 0.00289028 | synonymous-codon | UBL7 | GRCh38.p7 | 15:74449294 | CCCAGCAGCTCCACT[A/G]TACCCCAGGGAGGCT | 84993 |
rs779231710 | snp | C/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74457893 | CATCTTTCTTGCCAG[C/T]TGGATCCTTTAGCTA | 84993 |
rs779308214 | snp | A/C/G | 3.67588e-05 | 0.00428699 | missense | UBL7 | GRCh38.p7 | 15:74449190 | CGTCTTCATACCTGG[A/C/G]TGCCAGGAGTCGGTG | 84993 |
rs779322624 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74449438 | CCAGCAATAGTTCTT[A/G]GGGAAACTCTTAAGT | 84993 |
rs779488061 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74446656 | CACGCAGAAATTTTC[A/G]CCTTTTTTTAAATGT | 84993 |
rs779608609 | snp | C/T | 9.95173e-05 | 0.00705328 | intron-variant | UBL7 | GRCh38.p7 | 15:74450906 | GGAAATCAGCCAGAT[C/T]CAGGAGGGAGAAGAG | 84993 |
rs779693215 | snp | A/T | 0.000185168 | 0.00962028 | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460642 | AAAACAAAAGACTAA[A/T]GTTTTCTTCATCCTT | 84993 |
rs779698135 | snp | A/C | | | intron-variant | UBL7 | GRCh38.p7 | 15:74456465 | CATCCCTTTGTTCCA[A/C]CCAGGCTTGTGCCTC | 84993 |
rs779702918 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | UBL7 | GRCh38.p7 | 15:74450765 | GCCTGAGCACGAGGA[A/G]AGAGAAGGTACCCTC | 84993 |
rs779761471 | snp | C/T | 1.65814e-05 | 0.00287931 | missense | UBL7 | GRCh38.p7 | 15:74446101 | GAGTTCATGGGGCTC[C/T]TCCAGCAAAGATGAG | 84993 |
rs779791002 | snp | C/T | 1.85931e-05 | 0.00304896 | intron-variant | UBL7 | GRCh38.p7 | 15:74449169 | CAGCCTTGATCTTCC[C/T]GGCCCCGTCTTCATA | 84993 |
rs779900578 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74455067 | TTGTTCATGATCCCC[A/G]AAAGGATTCCAGGGC | 84993 |
rs780161895 | snp | A/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74452165 | CTGAGGCCCACAGAC[A/T]TGGCAAAAACTCCCC | 84993 |
rs780340307 | snp | C/G | 1.64914e-05 | 0.00287149 | intron-variant | UBL7 | GRCh38.p7 | 15:74456524 | TATTACAGAAACTCT[C/G]CCTGCCTAAGGGCTG | 84993 |
rs780391071 | snp | C/T | | | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445646 | ATAGACTGGACATCT[C/T]GGAAGCATAAGCCTC | 84993 |
rs780399139 | in-del | -/GT | 1.64895e-05 | 0.00287132 | intron-variant | UBL7 | GRCh38.p7 | 15:74449887 | AAGCAAATTCCTGGG[-/GT]CCACTGCCGGCTCCT | 84993 |
rs780556106 | snp | C/G | 1.65375e-05 | 0.0028755 | synonymous-codon | UBL7 | GRCh38.p7 | 15:74458796 | TTCTGTCTCTGGCAA[C/G]CGAAGAATAGACTTT | 84993 |
rs780570834 | snp | A/G | 2.39909e-05 | 0.00346336 | intron-variant | UBL7 | GRCh38.p7 | 15:74449890 | GCAAATTCCTGGGCC[A/G]CTGCCGGCTCCTGAG | 84993 |
rs780581061 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460241 | AGACTCCGTCCCTCC[C/T]TGCCCCACCCCGGCC | 84993 |
rs780926220 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74457678 | GGAGACAGAGGTTAC[A/G]ATGAGCTGAGATCTC | 84993 |
rs781019077 | snp | C/T | 1.82417e-05 | 0.00302002 | missense | UBL7 | GRCh38.p7 | 15:74449996 | AGTCAGTCCCAGGCA[C/T]TGGGGCACTGCCTGC | 84993 |
rs781113904 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | UBL7 | GRCh38.p7 | 15:74448444 | CAAAATAACAAGGAA[A/G]CCACATGGAAACCAA | 84993 |
rs781127989 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74460648 | AAAGACTAAAGTTTT[C/T]TTCATCCTTGTCCCC | 84993 |
rs781387559 | snp | G/T | 1.64743e-05 | 0.00287 | synonymous-codon | UBL7 | GRCh38.p7 | 15:74451479 | TGGGGTGGCCACAAT[G/T]ATCTGATCCAGAGAC | 84993 |
rs781484511 | snp | G/T | | | downstream-variant-500B | UBL7 | GRCh38.p7 | 15:74445857 | CATCCTCCATCCAGG[G/T]CCCAGAACTAGGGGC | 84993 |
rs781496141 | in-del | -/CC | 1.65803e-05 | 0.00287922 | frameshift-variant | UBL7 | GRCh38.p7 | 15:74458840 | GGTCAGCCAGCTTCA[-/CC]GCCAGGTGCCAGTCT | 84993 |
rs781506703 | snp | C/T | 1.67981e-05 | 0.00289806 | intron-variant | UBL7 | GRCh38.p7 | 15:74458634 | TCCAGAAGTATCCTC[C/T]CCCAAAAGAGATCAG | 84993 |
rs781524001 | in-del | -/T | | | frameshift-variant | UBL7 | GRCh38.p7 | 15:74458763 | AATACTATAGCCCCC[-/T]AGCGAGTATTCTCCC | 84993 |
rs781596740 | snp | A/T | 3.30082e-05 | 0.00406239 | intron-variant | UBL7 | GRCh38.p7 | 15:74449622 | AGGCAGGCAGGCCAC[A/T]TACTGGGTGAAAGTC | 84993 |
rs781681551 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | UBL7, UBL7-AS1 | GRCh38.p7 | 15:74461843 | TTAGATAACAGAAAG[A/T]TCTGCACGGTTAAAA | 84993 |
rs781700298 | in-del | -/GGGCCCAC | 2.34533e-05 | 0.00342434 | intron-variant | UBL7 | GRCh38.p7 | 15:74449906 | CTGCCGGCTCCTGAG[-/GGGCCCAC]ATTACACTTTTCAGG | 84993 |
rs781734089 | snp | C/T | | | intron-variant | UBL7 | GRCh38.p7 | 15:74447149 | AAGACAAGTTGTTCA[C/T]GAATCCTGCTTCTGT | 84993 |
rs796312780 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74454618 | GGTCAGGCTTGTCTC[A/G]AACTCCCAATCTCAG | 84993 |
rs796824860 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74447524 | GCTGGGCAACATAGG[A/G]AGACCCCCCCATCTC | 84993 |
rs796919603 | snp | A/G | | | intron-variant | UBL7 | GRCh38.p7 | 15:74450436 | TCTTCCCAGGGTGGG[A/G]CTGTTTTCTTCACTT | 84993 |