SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3655520 | snp | A/C | 0.5 | 0 | intron-variant | Utp18 | Mm_Celera | 11:93874505 | AGGGTGAGAAAGGGT[A/C]GAAAAAAGAACCCAC | 217109 |
rs3656040 | snp | C/T | 0.5 | 0 | intron-variant | Utp18 | GRCm38.p3 | 11:93874562 | TTCATTCTACCACCT[C/T]AACTGCTAAAATTAA | 217109 |
rs3656691 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | Utp18 | GRCm38.p3 | 11:93874669 | GGTTCTGTTCCCAGC[A/C]CCCACACGGAGACTC | 217109 |
rs4138210 | snp | A/G | 0.5 | 0 | intron-variant | Utp18 | GRCm38.p3 | 11:93874596 | CAAGTATCGGAGGCT[A/G]AAGAGATGATGGCTA | 217109 |
rs6182551 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Utp18 | GRCm38.p3 | 11:93862846 | GCAACATGACTCAGA[C/T]TGAAAGACTGACAGC | 217109 |
rs6182616 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Utp18 | GRCm38.p3 | 11:93862893 | AACTCAACATACCAA[A/C]CGGGGAAGCCATCCC | 217109 |
rs6182628 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Utp18 | GRCm38.p3 | 11:93862898 | AACATACCAAACGGG[C/G]AAGCCATCCCTAGTC | 217109 |
rs13470834 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Utp18 | GRCm38.p3 | 11:93869840 | TGCGGCATCCACATT[C/T]TCTTCAGATAGTAAG | 217109 |
rs13470835 | snp | C/T | 0.495868 | 0.0452663 | synonymous-codon | Utp18 | Mm_Celera | 11:93868360 | ATTGAGCATTGCTGC[C/T]TCAAAGAATGGACAG | 217109 |
rs28260420 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Utp18 | Mm_Celera | 11:93869647 | TGTTAACACTACATA[C/T]CAAATGGTTAACCCT | 217109 |
rs28260421 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93869605 | CCTTAAAACTTCCCA[C/T]ACTGAAGTGTGTATA | 217109 |
rs28260422 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Utp18 | Mm_Celera | 11:93869541 | TTGACCTTCTACATA[C/T]AACTCATGTTCCCAA | 217109 |
rs28260423 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Utp18 | Mm_Celera | 11:93869479 | CCTCAAAGAATGCTC[C/T]TCACTCCCTCTCATC | 217109 |
rs28260424 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Utp18 | Mm_Celera | 11:93869461 | ATACAATACTCACAT[C/T]CACCTCAAAGAATGC | 217109 |
rs28260425 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93868876 | TTCAAGTCATTATTA[C/T]GTAAGCAATATCACA | 217109 |
rs28260426 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93868317 | CTTAGCACGATGTGA[C/T]TCTCTTCACTTACCC | 217109 |
rs28260427 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Utp18 | GRCm38.p3 | 11:93868227 | TTACAAAATCAAAAG[A/G]CTCAGCTAGGATTAC | 217109 |
rs28260428 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93867364 | GATTTGACTTATCCT[A/G]TACCAACAAAATGAG | 217109 |
rs28260429 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Utp18 | GRCm38.p3 | 11:93867297 | GAAATCCCTAACTGC[A/G]ATTTCTTTATAGCTC | 217109 |
rs28260430 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Utp18 | GRCm38.p3 | 11:93867222 | AAGTAGCTTCCCCAA[C/T]TTTAATCTTGAGAAA | 217109 |
rs28260431 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Utp18 | GRCm38.p3 | 11:93867167 | TCCCAGCTCAGTTCA[A/C]CTTGACTTCCCAGGT | 217109 |
rs28260432 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Utp18 | Mm_Celera | 11:93867047 | CACCAGCCATCCTGG[A/G]CACTGCCTGTATGTA | 217109 |
rs28260433 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Utp18 | GRCm38.p3 | 11:93866734 | AGACTGTATTAAACA[C/T]CCACTCTGCCACGTA | 217109 |
rs28260434 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93866571 | ACCTCTGCAACCTAG[A/G]TGAAATAACATGCCA | 217109 |
rs28260435 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | Mm_Celera | 11:93866029 | CTAGTTGAACCCAAA[A/G]GCTCCCAACTAATAT | 217109 |
rs28260436 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93865070 | TGTAAAACACAAACC[A/G]CCAGTGTTCACATAA | 217109 |
rs28260437 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | Mm_Celera | 11:93865036 | CTAAGTTCATACTCA[A/G]TGAAATGTAAAAAGT | 217109 |
rs28260438 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Utp18 | GRCm38.p3 | 11:93865010 | AATCTTCATAAAACA[C/T]ACACTATCATCTAAG | 217109 |
rs28260439 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93864130 | GCAAACCTAAAAACT[A/C]AGGGAAGGAGAAAGA | 217109 |
rs28260440 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93862160 | CTTATCCTTTCCCAA[A/T]TTTTTTCACTCTATC | 217109 |
rs28260441 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Utp18 | GRCm38.p3 | 11:93861490 | TGCCTGTTTTAAAGA[C/T]AAGTATTTGGGTAAA | 217109 |
rs28260442 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Utp18 | Mm_Celera | 11:93861467 | ATGGTGCAATTAAAT[C/T]TTGCTTATGCCTGTT | 217109 |
rs28260443 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Utp18 | GRCm38.p3 | 11:93861434 | CCTTGAAGAGTCACC[G/T]TTCACCATATTCTAG | 217109 |
rs28260444 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | Mm_Celera | 11:93860859 | AGGCAAAAGAGAACT[A/G]TTTAGCCACAGAGTT | 217109 |
rs28260445 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Utp18 | GRCm38.p3 | 11:93860743 | AACCAAATGACATCA[A/G]TGGCACACCCTAAAC | 217109 |
rs28260446 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Utp18 | Mm_Celera | 11:93860664 | TTTGCACCCACTTCC[A/C]TAAATTGAAGATGTA | 217109 |
rs28260447 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Utp18 | Mm_Celera | 11:93860636 | TTCAGGTCAGTTAGA[C/T]AGCTCCTGATCATTT | 217109 |
rs28260448 | snp | A/G/T | 0.165289 | 0.235211 | intron-variant | Utp18 | GRCm38.p3 | 11:93860600 | ACCATTGTGACTGGG[A/G/T]TTAGAAATTCCCAAG | 217109 |
rs28260449 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Utp18 | GRCm38.p3 | 11:93859863 | TTTTTATTACAGACA[A/G]GTTTCCATTTCTCAC | 217109 |
rs28260450 | snp | G/T | 0.46875 | 0.121031 | utr-variant-3-prime | Utp18 | Mm_Celera | 11:93859761 | AAAAAAAAAAAAGGC[G/T]ACTGGATAGTTTTAA | 217109 |
rs29385348 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93877696 | AAGCACAGGTTGCTA[A/C]GATTAATGAATGTAA | 217109 |
rs29385454 | snp | A/G | 0.5 | 0 | intron-variant | Utp18 | Mm_Celera | 11:93877638 | ATGTTTAGCACACAG[A/G]TCTGTTCGTTTGACA | 217109 |
rs29386555 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Utp18 | Mm_Celera | 11:93871659 | AAATGTACCTAATGC[A/C]GTGGGAAATGCAGAT | 217109 |
rs29386724 | snp | A/G | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93883529 | CTTTCTCTCAGATAC[A/G]AATTATGAACCTTTT | 217109 |
rs29390875 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93879068 | AGAGGTAGAGGCAGG[C/T]AGACCCTAAACTCAG | 217109 |
rs29393693 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93873445 | GATGAGACAGGATGG[C/T]ATCCTATAGAAAGGA | 217109 |
rs29396059 | snp | C/T | 0.5 | 0 | intron-variant | Utp18 | GRCm38.p3 | 11:93871878 | GAAGACTGCCAGTAA[C/T]CTATGGCTATGTCAA | 217109 |
rs29399471 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Utp18, Mbtd1 | GRCm38.p3 | 11:93884026 | GAAGGGGGTGGGGGG[A/G]GGAAGTGCACGGAAA | 217109 |
rs29400046 | snp | A/G | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93877493 | AACCTTTATAGTAGA[A/G]GTGCTTCAATTTCAA | 217109 |
rs29402298 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Utp18, Mbtd1 | Mm_Celera | 11:93885049 | TGGCAAACCAAGCCG[A/G]CAGTTGAGCGCCTGC | 217109 |
rs29402986 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Utp18 | Mm_Celera | 11:93867823 | GCTGCCTACCTGCTA[C/T]CACTGCTCCCTCCCT | 217109 |
rs29403087 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93883828 | TGATTCTCCAACAAG[G/T]TGCTAGCGCACACGC | 217109 |
rs29405175 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Utp18 | Mm_Celera | 11:93870111 | GTGAGTACTGAGAAC[C/T]GAACTCAGATCCTGT | 217109 |
rs29407978 | snp | A/G | 0.5 | 0 | intron-variant | Utp18 | GRCm38.p3 | 11:93875562 | CATGGAGAGCTGGGT[A/G]TGATGGCACTGGCAC | 217109 |
rs29408059 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93871614 | ACAGTAGCTGTCAAA[A/G]CAAGGGCTTTTCAAC | 217109 |
rs29408092 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | Mm_Celera | 11:93868770 | CTATTATTTAAGGCT[A/G]TACAATATAAATAAG | 217109 |
rs29408670 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93871631 | AAGGGCTTTTCAACA[G/T]TCACTGACCAGGAAA | 217109 |
rs29410422 | snp | A/G | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93883553 | ACCTTTTTCCTGTGC[A/G]CCAAATGTTTTGGTT | 217109 |
rs29414226 | snp | C/T | 0.375 | 0.216506 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Utp18, Mbtd1 | Mm_Celera | 11:93885481 | GCTCTCCTCCTCCTC[C/T]GCCGCCGCCGCCGCG | 217109 |
rs29416229 | snp | C/G | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93865627 | ATCCTGCTTAGTATC[C/G]TATGGCTGTAATAAA | 217109 |
rs29419540 | snp | C/T | 0.5 | 0 | intron-variant | Utp18 | GRCm38.p3 | 11:93873371 | TGATGACATGACCAC[C/T]ATCAGCTTTCCCAGT | 217109 |
rs29423726 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Utp18, Mbtd1 | GRCm38.p3 | 11:93885427 | CTCGGCGGCCGGCTT[A/G]TCGTCCTCTAGCGTC | 217109 |
rs29424590 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Utp18, Mbtd1 | GRCm38.p3 | 11:93885950 | CATATTGGAAGGGAC[A/T]CGAGGAGGCCGGAGT | 217109 |
rs29426464 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93877725 | AAACAAACTTTGGTG[C/T]GGGTAAACCAAGTAC | 217109 |
rs29426945 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93863189 | CCCATAATCAGCCAC[A/C]AAACCCAGACACTAT | 217109 |
rs29428323 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93863829 | AACACCAGGCATGCA[A/G]ATGGAACACATATGC | 217109 |
rs29428839 | snp | C/G | 0.375 | 0.216506 | intron-variant | Utp18 | Mm_Celera | 11:93871952 | CTGCTTTGGTTCCCC[C/G]ACTCCCCCGCCAAAA | 217109 |
rs29428901 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93879021 | CCAGAATACTGTACA[A/G]GAAAACTATAGGTGC | 217109 |
rs29431416 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Utp18, Mbtd1 | Mm_Celera | 11:93885157 | CGAGGCGAAAGAGCC[C/G]GACGGCGCCCCTCGG | 217109 |
rs29432335 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Utp18 | Mm_Celera | 11:93867706 | GTGTCACTGTGTGGG[A/C]TTTAAAGTTTCAAAA | 217109 |
rs29432592 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Utp18 | Mm_Celera | 11:93868158 | TAGCAGGGTTTTTTT[A/G]TTTTTGCCAAAAAGT | 217109 |
rs29440393 | snp | C/T | 0.375 | 0.216506 | intron-variant | Utp18 | Mm_Celera | 11:93877659 | TCGTTTGACAGATAA[C/T]AGCTGAAGCACTGAG | 217109 |
rs29442268 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93863599 | ATAGGAAACTTTCGG[A/G]ATAACATTTGAAATG | 217109 |
rs29446145 | snp | C/T | 0.375 | 0.216506 | intron-variant | Utp18 | Mm_Celera | 11:93877497 | TTTATAGTAGAGGTG[C/T]TTCAATTTCAAGGAG | 217109 |
rs29446435 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93863525 | ATGCCCCAGTACAGG[A/G]GAACGCCAGGGCCAA | 217109 |
rs29447750 | snp | C/G | 0.375 | 0.216506 | intron-variant | Utp18 | Mm_Celera | 11:93865777 | GCACCTTTAATTATG[C/G]AACTCAACTGACTTT | 217109 |
rs29450326 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Utp18, Mbtd1 | Mm_Celera | 11:93885767 | AGCCGGAAGGAGTCT[A/G]CGCCGCCGCAAGCCA | 217109 |
rs29454193 | snp | C/T | 0.5 | 0 | intron-variant | Utp18 | Mm_Celera | 11:93873608 | GAAGCCAGCCCACAA[C/T]TGCAATGGTTAACAA | 217109 |
rs29457719 | snp | A/T | 0.5 | 0 | intron-variant | Utp18 | Mm_Celera | 11:93864664 | AGTATCTATCATTGG[A/T]CACACATGGCCCATG | 217109 |
rs29458834 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93873418 | CCTGCTAATGGTGTG[A/G]AACAAGGTTATGATG | 217109 |
rs29461048 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Utp18, Mbtd1 | GRCm38.p3 | 11:93885953 | ATTGGAAGGGACACG[A/G]GGAGGCCGGAGTCCA | 217109 |
rs29463321 | snp | G/T | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93865408 | TTACTCCTAGGCACC[G/T]AGAATTCAGCAAATG | 217109 |
rs29463855 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93863306 | GGATGCTCACAGTCA[G/T]CTATTGGATGGACCG | 217109 |
rs29468879 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Utp18 | Mm_Celera | 11:93867722 | TTTAAAGTTTCAAAA[A/C]CCCTGGCCAGGCCCA | 217109 |
rs29470251 | snp | C/T | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93871894 | CTATGGCTATGTCAA[C/T]TCTGGCACAAGATGT | 217109 |
rs29471091 | snp | A/T | 0.375 | 0.216506 | intron-variant | Utp18 | GRCm38.p3 | 11:93865695 | TCTTTCCATTAAATC[A/T]TAAGAACTGGGTGGT | 217109 |
rs29473238 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Utp18 | GRCm38.p3 | 11:93867266 | CCACCCCCACTAACG[C/T]CCCACTCCAGGGCAA | 217109 |
rs29474649 | snp | A/G | 0.32 | 0.24 | intron-variant | Utp18 | GRCm38.p3 | 11:93868103 | CGTGATCAAATGAGT[A/G]TTCTAAATTCAGGAA | 217109 |
rs29486526 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Utp18, Mbtd1 | Mm_Celera | 11:93884361 | ACTGCAGTATCCACC[A/C]GCACTGCTGATTTAA | 217109 |
rs33849296 | snp | G/T | 0.375 | 0.216506 | intron-variant | Utp18 | Mm_Celera | 11:93864621 | TTGCAATCTGCCACT[G/T]TCATCTACAAGTGTG | 217109 |
rs45649290 | snp | A/T | | | intron-variant | Utp18 | GRCm38.p3 | 11:93881637 | GTAATTCCATTTTTT[A/T]AAATTTTTCATATCC | 217109 |
rs45677863 | snp | A/T | | | intron-variant | Utp18 | GRCm38.p3 | 11:93880856 | TCTGTCTCAAAAATC[A/T]AAAGTACAAAATAAA | 217109 |
rs45722483 | snp | C/T | | | downstream-variant-500B | Utp18 | GRCm38.p3 | 11:93858946 | AGCAGTTCAAGAGCA[C/T]GCACAGCACCTGTAA | 217109 |
rs45807321 | snp | C/T | | | intron-variant | Utp18 | GRCm38.p3 | 11:93880008 | AGCTTGGGAAAACTC[C/T]AATAAAAACAGTACA | 217109 |
rs45947189 | snp | C/T | | | downstream-variant-500B | Utp18 | GRCm38.p3 | 11:93858773 | CTGGAGAAAAATAAA[C/T]TTGCTTCATGGAGTT | 217109 |
rs46108533 | snp | A/G | | | intron-variant | Utp18 | Mm_Celera | 11:93876327 | TTACAATTCATAACA[A/G]TGGCAAAATTACAAT | 217109 |
rs46116990 | snp | A/G | | | intron-variant | Utp18 | GRCm38.p3 | 11:93876196 | CTGTGGAAATAAAAG[A/G]CTGGGAGGTTATCGA | 217109 |
rs46125729 | snp | A/T | | | intron-variant | Utp18 | GRCm38.p3 | 11:93879553 | ATTCATTTATCCTCT[A/T]TCTTCCTTACAGTAA | 217109 |
rs46244679 | snp | A/G | | | intron-variant | Utp18 | GRCm38.p3 | 11:93881621 | AGCCCATATATAATG[A/G]GTAATTCCATTTTTT | 217109 |
rs46360164 | snp | C/T | | | intron-variant, downstream-variant-500B | Utp18 | Mm_Celera | 11:93870212 | TTCCCTATATCTTCT[C/T]CTAAAGTTCTACTTG | 217109 |