SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs166760 | snp | C/T | 0.168135 | 0.236216 | intron-variant | UBL3 | GRCh38.p7 | 13:29846101 | TTGCAGTGTGACTTA[C/T]GTTAACCACTGTAGG | 5412 |
rs175875 | snp | A/G | 0 | 0 | intron-variant | UBL3 | GRCh38.p7 | 13:29847845 | TTCAAGAGCAGTATG[A/G]AGGAAAGCTTGTCCA | 5412 |
rs278031 | snp | A/C | 0.168135 | 0.236216 | intron-variant | UBL3 | GRCh38.p7 | 13:29845421 | TTTATTTTTCTTTCT[A/C]TTCCTGATGATTCTT | 5412 |
rs278032 | snp | A/G | 0.168135 | 0.236216 | intron-variant | UBL3 | GRCh38.p7 | 13:29844800 | TAAAATACTGATGGT[A/G]CTAATAGTTTTCACA | 5412 |
rs278033 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29842825 | CCAGAAAATTAGCCC[C/T]CCTAAAAAGAGAATT | 5412 |
rs278034 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | UBL3 | GRCh38.p7 | 13:29842500 | gcaggatctggcata[C/T]gctcttcctagctgc | 5412 |
rs278035 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29842060 | CCTCCAGTTGATGTA[C/T]GATAGCATTCAGTCC | 5412 |
rs278036 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29841748 | GCCACCAGACCCAAA[C/T]TCCTATTCTAGCTCA | 5412 |
rs278037 | snp | A/G | 0.302686 | 0.244385 | utr-variant-5-prime | UBL3 | GRCh38.p7 | 13:29850490 | AACAAAGCTCTGAGA[A/G]GAAACCATTCCCGGG | 5412 |
rs278038 | snp | A/G | 0.16976 | 0.236773 | intron-variant | UBL3 | GRCh38.p7 | 13:29848314 | AAAAAAAAATTAGCC[A/G]GGTGTGGTGGTGGGC | 5412 |
rs278039 | snp | C/T | 0.132751 | 0.2208 | intron-variant | UBL3 | GRCh38.p7 | 13:29847334 | ATATTATGTAATAAA[C/T]ATATAATGCCCTGAT | 5412 |
rs541881 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBL3 | GRCh38.p7 | 13:29838770 | ATACAAATTGCAAAA[C/T]TGTAAATTCAAACCC | 5412 |
rs719199 | snp | C/G | 0.192401 | 0.243274 | intron-variant | UBL3 | GRCh38.p7 | 13:29815115 | GCTACTGTGTTTTGC[C/G]CAGAGTTAGGACAAT | 5412 |
rs720083 | snp | C/T | 0.413582 | 0.189052 | intron-variant | UBL3 | GRCh38.p7 | 13:29775100 | CACTATGTAGGAACA[C/T]AGGCATGACAAACTC | 5412 |
rs751164 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | UBL3 | GRCh38.p7 | 13:29852476 | TACAGTGGCACTTAG[G/T]CCCGGCAGTGCCATG | 5412 |
rs751388 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBL3 | GRCh38.p7 | 13:29851660 | GTCTTGCCTACCTTC[C/T]GGGGTAAAGTAGGGG | 5412 |
rs765404 | snp | A/G | 0.413748 | 0.188909 | intron-variant | UBL3 | GRCh38.p7 | 13:29845084 | TTTAGTGCTTTTGAC[A/G]TTCCTCTTACACAGG | 5412 |
rs818763 | snp | A/C | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29823990 | ctggaaaccatcatt[A/C]tcagcaaactatcgc | 5412 |
rs818764 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29823815 | acctaatgtaaatga[C/T]gagttaatgggtgca | 5412 |
rs957189 | snp | C/T | 0.426813 | 0.17674 | intron-variant | UBL3 | GRCh38.p7 | 13:29844582 | TCCAACATTGTTAGA[C/T]TGGGCTATCTTAACA | 5412 |
rs968612 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29840644 | TTTCCTAATTTTAAA[A/G]CATCCTTGAATTTCT | 5412 |
rs980524 | snp | G/T | 0.138886 | 0.22395 | intron-variant | UBL3 | GRCh38.p7 | 13:29819113 | CTCAGCTTCAACAGT[G/T]GTCACCTCATAGACA | 5412 |
rs1058647 | snp | C/T | 0 | 0 | utr-variant-5-prime | UBL3 | GRCh38.p7 | 13:29849586 | CTTCTGCTCTTTTTT[C/T]TTTGTTTGTTTTTTT | 5412 |
rs1058650 | snp | A/G | 0.414245 | 0.188477 | utr-variant-3-prime | UBL3 | GRCh38.p7 | 13:29766448 | CTTTCATTATTGTGC[A/G]GAAATATTAGAAAAC | 5412 |
rs1323931 | snp | C/T | 0.319136 | 0.24025 | intron-variant | UBL3 | GRCh38.p7 | 13:29811373 | TGCTTCATTTTAAAA[C/T]ACTCTTAGGAAGGAA | 5412 |
rs1327643 | snp | A/T | 0.131723 | 0.220251 | intron-variant | UBL3 | GRCh38.p7 | 13:29774548 | TCTTAGATCCCAAAT[A/T]TCTTTAGCTTTTCTG | 5412 |
rs1408175 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBL3 | GRCh38.p7 | 13:29817537 | TTTCAGCTATTTTGC[C/T]TCTGGTCTCTTTCCT | 5412 |
rs1410110 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | UBL3 | GRCh38.p7 | 13:29790880 | CTGGGAGAGAGACTG[A/G]TGAGGGAACCTTGGA | 5412 |
rs1631987 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29833136 | CATGCTAATCCAGGC[C/T]AACCTTCTTACCATG | 5412 |
rs1747057 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29832028 | CACGTGGCTACCTTA[C/T]TAGACGACACAATAA | 5412 |
rs1747058 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | UBL3 | GRCh38.p7 | 13:29832187 | CCTCAGAGTAAGTAC[A/G]TAGTCTGTTTAGTGG | 5412 |
rs1747059 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29832457 | CCTGCGTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5412 |
rs1747060 | snp | A/C | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29833261 | CAGTGGATGACTAAA[A/C]TAAAAAGACGTCTGG | 5412 |
rs1747061 | snp | A/G | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29835915 | acatagtcatgttag[A/G]caggagctagatcat | 5412 |
rs1747062 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29836214 | GATGGCTCCAAGAGA[C/T]GTCTGACTTAAGCAA | 5412 |
rs1747063 | snp | C/T | 0.170733 | 0.237101 | intron-variant | UBL3 | GRCh38.p7 | 13:29837704 | GGAGGCTGAGGCAGG[C/T]GGATCACTTGAGGCC | 5412 |
rs1772726 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29828740 | ATCAGAGCGCCTGTT[C/T]CCCTCCAAACAATGC | 5412 |
rs1772727 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | UBL3 | GRCh38.p7 | 13:29830559 | GAAACAACATCTCTT[C/T]GCAATCTCTGCATCA | 5412 |
rs1886170 | snp | A/G | 0.303938 | 0.244112 | intron-variant | UBL3 | GRCh38.p7 | 13:29816284 | TCCATAATTTAGTCA[A/G]TTTCTTCAATACCAT | 5412 |
rs2025604 | snp | A/G | 0.427119 | 0.176434 | intron-variant | UBL3 | GRCh38.p7 | 13:29842202 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC | 5412 |
rs2031280 | snp | A/G | 0.139225 | 0.224118 | intron-variant | UBL3 | GRCh38.p7 | 13:29779699 | tgtggctatctgttc[A/G]tgtcagatcatacag | 5412 |
rs2182129 | snp | A/C | 0.412416 | 0.190055 | intron-variant | UBL3 | GRCh38.p7 | 13:29846172 | ATGATGTATTTATTT[A/C]TTTATGTTGCAGCCA | 5412 |
rs2234413 | snp | C/G | 0.0178098 | 0.0926698 | utr-variant-5-prime | UBL3 | GRCh38.p7 | 13:29850393 | AGGCCGGGGAGGGGA[C/G]GGGAAGGGAAGGCGG | 5412 |
rs2234414 | snp | G/T | 0.0178098 | 0.0926698 | utr-variant-5-prime | UBL3 | GRCh38.p7 | 13:29850049 | CCGCGGCCAGCGTCC[G/T]GCCACCGCTCGGCCG | 5412 |
rs2234415 | snp | A/T | 0.00299555 | 0.038585 | intron-variant | UBL3 | GRCh38.p7 | 13:29772088 | CACCTTTGTAATGGG[A/T]TTTAATGTCTGTCTC | 5412 |
rs2234416 | snp | G/T | 0.413914 | 0.188765 | intron-variant | UBL3 | GRCh38.p7 | 13:29772051 | GCATGATTCGCTTGT[G/T]TTAAATGTTAATGTC | 5412 |
rs2234417 | snp | A/G | 0.093417 | 0.194889 | intron-variant | UBL3 | GRCh38.p7 | 13:29771996 | AAATTCAAACTATGA[A/G]TTCTGCCTATTTCTG | 5412 |
rs2256122 | snp | A/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29830632 | CTTACAAAGGTGAAT[A/T]TTTCTATTACAGAAT | 5412 |
rs2388244 | snp | A/G | 0.306182 | 0.243605 | intron-variant | UBL3 | GRCh38.p7 | 13:29799201 | CATTCCACCCTTGCC[A/G]CCTTCCCCTTCCCCC | 5412 |
rs2388245 | snp | C/G | 0.303688 | 0.244167 | intron-variant | UBL3 | GRCh38.p7 | 13:29839751 | GCTAACACGGTGAGA[C/G]CCCGTCTCTACTAAA | 5412 |
rs2388246 | snp | A/G | 0.426966 | 0.176587 | intron-variant | UBL3 | GRCh38.p7 | 13:29840806 | ATGTCATTGTTTGTA[A/G]TAGCTTCTAAATGCT | 5412 |
rs2388247 | snp | A/G | 0.425432 | 0.178112 | upstream-variant-2KB | UBL3 | GRCh38.p7 | 13:29852216 | CAAGTCCATAGTTAC[A/G]TGATTTTCCATGGCC | 5412 |
rs2476650 | snp | A/C | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29826290 | ccagctcctccttgt[A/C]cctctgctagaattc | 5412 |
rs2476651 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29828194 | GTATCTTTGTGGCAT[C/T]CTCTGTATTTCCTGA | 5412 |
rs2487664 | snp | G/T | 0.422315 | 0.181128 | intron-variant | UBL3 | GRCh38.p7 | 13:29831182 | AAAAAGTATAAATTT[G/T]TGTGAGCATTCAGTT | 5412 |
rs2761929 | snp | A/C | 0.16976 | 0.236773 | intron-variant | UBL3 | GRCh38.p7 | 13:29827042 | TGATTGCACTGTGGT[A/C]TGAGAGACAGTTTGT | 5412 |
rs2761930 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29827343 | GTAGGTCTCCAAGGA[C/T]TTGCTTTATGAATCT | 5412 |
rs2761931 | snp | A/C | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29828280 | GCAGAGTGTTTTCCA[A/C]CTTGGTTCCATTCTC | 5412 |
rs2761932 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29828345 | TTTGGTCTATTCACA[C/T]AGTCCCGTATTTCTT | 5412 |
rs2761934 | snp | A/G | 0.170408 | 0.236992 | intron-variant | UBL3 | GRCh38.p7 | 13:29828972 | CTGGGTATCAGCAGC[A/G]GAGGCTGCAGAACAG | 5412 |
rs2761936 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29831653 | CTTTCTATATGATAG[C/T]TGACTAAAATCAGAA | 5412 |
rs2761937 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBL3 | GRCh38.p7 | 13:29831807 | CACTTGGAATACAAG[C/T]CAAAAACAAACAAAC | 5412 |
rs2761938 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | UBL3 | GRCh38.p7 | 13:29833859 | AGCACCTAAAAAAGC[A/G]TCTGACACATAGGAG | 5412 |
rs2761939 | snp | A/C | 0.480539 | 0.0967035 | intron-variant | UBL3 | GRCh38.p7 | 13:29834601 | TGGCTTAATGATAAA[A/C]AAATGTTAAAATTCA | 5412 |
rs2761940 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | UBL3 | GRCh38.p7 | 13:29835733 | gcactccagcctggc[A/G]acagagctagacgct | 5412 |
rs2794295 | snp | C/T | 0.168135 | 0.236216 | intron-variant | UBL3 | GRCh38.p7 | 13:29837787 | GCATATCACCACGCC[C/T]GGCTAATTTTTGTAT | 5412 |
rs2794296 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29834131 | CACTGTGGCGCGATC[G/T]CAGCTCACTGGAAGC | 5412 |
rs2794297 | snp | A/C | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29822794 | TCACTCAAAAGAAAA[A/C]CTTTAGTTCTTTGAG | 5412 |
rs2794298 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | UBL3 | GRCh38.p7 | 13:29819313 | TTGGCCTTTGCCTTT[A/C/T]GTTTTACGCTTCATA | 5412 |
rs2794299 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29818682 | ATATACAAGCTGTTA[C/T]ACATTGGCCACTAAG | 5412 |
rs2794300 | snp | C/G | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29818142 | TTCCTTTTTTCACTG[C/G]TTGGTGCAGTTAAGG | 5412 |
rs2892463 | snp | G/T | 0.498852 | 0.0239341 | intron-variant | UBL3 | GRCh38.p7 | 13:29773698 | CTTCCCCTCTCCAGG[G/T]ATCTAAAATTTAGAG | 5412 |
rs2892464 | snp | C/T | 0.168135 | 0.236216 | intron-variant | UBL3 | GRCh38.p7 | 13:29839693 | agcactttgggaggc[C/T]gaggcgggaggatca | 5412 |
rs3118078 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29817941 | ACAGAAAATAACTTA[C/T]ACTAGCCTGAACTGA | 5412 |
rs3118079 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29820229 | acccaggctggagag[C/T]tcagtggctcgatct | 5412 |
rs3118080 | snp | C/T | 0.170084 | 0.236883 | intron-variant | UBL3 | GRCh38.p7 | 13:29820245 | TCAGTGGCTCGATCT[C/T]GGCTCACTGCAACCT | 5412 |
rs3759515 | snp | C/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | UBL3 | GRCh38.p7 | 13:29850851 | GCAGCTTGTCCAAAG[C/G]AAGGGAAAGGGAGCT | 5412 |
rs3783244 | snp | C/T | 0.412917 | 0.189626 | intron-variant | UBL3 | GRCh38.p7 | 13:29778780 | AGGGGAGATATTTTA[C/T]AACTTTCAACAAAAT | 5412 |
rs3818368 | snp | C/T | 0.19098 | 0.242933 | intron-variant | UBL3 | GRCh38.p7 | 13:29777129 | TTTTTCTCTTGAGTA[C/T]GAATAATGTTGATTC | 5412 |
rs4083609 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29784588 | tcccttgatatAAGT[C/T]GGGAGTTGTTTTTTT | 5412 |
rs4083610 | snp | C/T | 0.493837 | 0.055168 | intron-variant | UBL3 | GRCh38.p7 | 13:29784429 | CCTAAGGAAGACTGG[C/T]ATGTGAAGTAAGAGT | 5412 |
rs4142339 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | UBL3 | GRCh38.p7 | 13:29770940 | CTCAGTGTGAGATTA[C/T]AGCCTGAAATGTTTT | 5412 |
rs4142340 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | UBL3 | GRCh38.p7 | 13:29786559 | ATTTCTCTCCCCCAC[C/T]GAAATGGGGCAGCAA | 5412 |
rs4238128 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | UBL3 | GRCh38.p7 | 13:29783806 | ATGGGATCCTTGACA[C/T]ATCAATAATGGGTTA | 5412 |
rs4265673 | snp | G/T | 0.480618 | 0.0965156 | intron-variant | UBL3 | GRCh38.p7 | 13:29791302 | TAAAATTCTGTCAGG[G/T]TGTTCTAGACAGCTA | 5412 |
rs4297554 | snp | A/C | 0.424503 | 0.179021 | intron-variant | UBL3 | GRCh38.p7 | 13:29796315 | CAGTTTTTAAAGTTA[A/C]CTTTAAGTTTTTACT | 5412 |
rs4385989 | snp | A/G | 0.131723 | 0.220251 | utr-variant-3-prime | UBL3 | GRCh38.p7 | 13:29766893 | ATGCCAATCTTTTTA[A/G]TGCAAATTGTATTTG | 5412 |
rs4387451 | snp | A/G | 0.424503 | 0.179021 | intron-variant | UBL3 | GRCh38.p7 | 13:29780303 | agcttgcagtgagcc[A/G]agattgtgccactgc | 5412 |
rs4389001 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | UBL3 | GRCh38.p7 | 13:29780140 | cgggaggatcacaag[A/G]tcaggagatcgagac | 5412 |
rs4399408 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29793146 | TATAGAATAGTAAAG[C/T]GCAAATTAAAATTGA | 5412 |
rs4611301 | snp | C/T | 0.17461 | 0.238362 | intron-variant | UBL3 | GRCh38.p7 | 13:29769223 | AGGTAAACTGAGATA[C/T]ATATGTAAAAAATGT | 5412 |
rs4769773 | snp | A/G | 0.0611083 | 0.163768 | utr-variant-3-prime | UBL3 | GRCh38.p7 | 13:29765957 | ATGGAATATTGTTCT[A/G]TATACTACGCGCCAA | 5412 |
rs4769774 | snp | A/G | 0.303938 | 0.244112 | intron-variant | UBL3 | GRCh38.p7 | 13:29780675 | CTGTTTACTAATAAG[A/G]TTGAGAAAAGGTATA | 5412 |
rs4769775 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | UBL3 | GRCh38.p7 | 13:29786934 | CAAATAAAACTTTTA[C/T]AACATATCATTTACT | 5412 |
rs4769777 | snp | A/G | 0.413914 | 0.188765 | intron-variant | UBL3 | GRCh38.p7 | 13:29841063 | TGAAAGTAAAGAAAA[A/G]CATATATCATAAGAA | 5412 |
rs5741722 | in-del | -/T | 0 | 0 | intron-variant | UBL3 | GRCh38.p7 | 13:29776280 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTTGC | 5412 |
rs5802530 | in-del | -/T | 0.0614824 | 0.164198 | intron-variant | UBL3 | GRCh38.p7 | 13:29784418 | AGTATTGGGATACTC[-/T]TACTTCACATGCCAG | 5412 |
rs5802531 | in-del | -/A | | | intron-variant | UBL3 | GRCh38.p7 | 13:29790770 | AACTAGTGTTTGGTT[-/A]AAACATCCTTCGGGA | 5412 |
rs5802532 | in-del | -/G | 0.375 | 0.216506 | intron-variant | UBL3 | GRCh38.p7 | 13:29822773 | CCTGTACTATCCTGT[-/G]GAAAAACTCAAAGAA | 5412 |
rs5802533 | in-del | -/TT | 0 | 0 | intron-variant | UBL3 | GRCh38.p7 | 13:29842158 | TTTTTTTTTTTTTTT[-/TT]AGAGACAGAGTCTTA | 5412 |