SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6158818 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70339883 | CACTTTCAAGAGGGC[A/G]TGGCCTCCACCATGC | 19704 |
rs6159335 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70339952 | TTTTATTCTACTTAT[A/G]GTCACAAATATTTTA | 19704 |
rs32536779 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70345259 | CGATCTAAAAGCTTT[C/T]AGACAAGGAAGATGC | 19704 |
rs32554973 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Upf1 | Mm_Celera | 8:70352172 | CTTAGACATACCTAG[A/G]AGGGGAGTGAGGGAA | 19704 |
rs32579000 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Upf1 | Mm_Celera | 8:70346285 | CAGCACTCTGTGGGG[C/T]GCATGGGATGACACA | 19704 |
rs32597249 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Upf1 | Mm_Celera | 8:70348781 | GCTGTGCAGAGCTGG[A/G]ACAGACTGACTGTCC | 19704 |
rs32598395 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Upf1 | Mm_Celera | 8:70333660 | AGCTGAGGTAGACAC[A/G]GGTTTGTTGCAGGAT | 19704 |
rs32611193 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Upf1 | Mm_Celera | 8:70334422 | TCTTGATCATGAGCT[A/C]AATCTGTGTCCTATA | 19704 |
rs32622456 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355279 | AAATAAATCTTTTTT[A/T]TAAAAAAAAAGTGAG | 19704 |
rs32626480 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70349578 | CTGCTCTCAGAGCCT[C/T]AGCATTTTGATCGAG | 19704 |
rs32665463 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Upf1 | GRCm38.p3 | 8:70348788 | AGAGCTGGGACAGAC[A/C/T]GACTGTCCCAAACCA | 19704 |
rs32673622 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Upf1 | Mm_Celera | 8:70333513 | GCCAGCCAGACAAGT[A/C]GGGAGGTCGAGTGTG | 19704 |
rs32682319 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70349577 | ACTGCTCTCAGAGCC[C/T]TAGCATTTTGATCGA | 19704 |
rs32701688 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70341087 | CCTGGGCATACTGAG[A/G]TAACTGGAACTTGAC | 19704 |
rs32736126 | snp | C/T | 0.489796 | 0.070696 | synonymous-codon | Upf1 | Mm_Celera | 8:70334752 | GTCCACACTGGCAAT[C/T]TCCACTTCCTGAATG | 19704 |
rs32746883 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70345140 | GTCAATTCCCAACAC[C/T]ACCAAAATACACCCT | 19704 |
rs32755200 | snp | A/C/G | 0.492188 | 0.0620098 | intron-variant | Upf1 | GRCm38.p3 | 8:70346437 | CCTCTTAATCCTCCT[A/C/G]CCCACACAGCACACC | 19704 |
rs32839614 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355133 | CAGATAAGAGCACCC[A/G]ACTGTTCTTCTGAAG | 19704 |
rs32862929 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Upf1 | Mm_Celera | 8:70347577 | ACAGCACCTTACACA[C/G]AACAGGGCCAGAGCC | 19704 |
rs32864843 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Upf1 | Mm_Celera | 8:70338743 | CATCCACATGAGGCA[C/G]GCCAGAGGGTTGTAG | 19704 |
rs32875723 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Upf1 | Mm_Celera | 8:70353528 | GGTGCGCATGCGCGC[A/C]TGCGACGTCCTCACC | 19704 |
rs32889655 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70341064 | TCACTGAGACAGAGA[A/G]CAGAGAACCTGGGCA | 19704 |
rs32925683 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Upf1 | Mm_Celera | 8:70348587 | GCTCACCCCTTGTCC[C/G]ACAGGCACACAGGAT | 19704 |
rs32934187 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Upf1 | Mm_Celera | 8:70335538 | CAAGAGCCTGTTTGC[A/G]TCTTCCCTCACATGC | 19704 |
rs32948417 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Upf1 | Mm_Celera | 8:70338592 | TAGGCTGTCAGCATC[A/G]CCCAGAGCAGCTCAG | 19704 |
rs32963692 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70354777 | GGGACAGTAGTGCCT[A/G]TAGCCACTGCTCAAT | 19704 |
rs32983281 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Upf1 | Mm_Celera | 8:70344584 | ACAAGATGATTGCTT[C/G]AAACCTGTCATACCA | 19704 |
rs32986323 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70341972 | TGGTCCCAGCAGACA[C/T]TGTCCTCTCCAGCCC | 19704 |
rs33018335 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Upf1 | Mm_Celera | 8:70336906 | ACACACTCCAGCAGC[A/C]CTGTGTCTGAGAAGC | 19704 |
rs33024179 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355278 | TAAATAAATCTTTTT[A/T]TTAAAAAAAAAGTGA | 19704 |
rs33036412 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Upf1 | Mm_Celera | 8:70332848 | TACTGCAGCCAGAGT[A/G]GCAGGGTGACAGGTT | 19704 |
rs33071107 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355517 | TTTAAACAAGACAAG[G/T]AATTGCTCAAGACCT | 19704 |
rs33082407 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70347789 | CACAGTAACATTTAG[A/G]CACACCCTAAAGTTC | 19704 |
rs33101528 | snp | A/G | 0.497778 | 0.0332592 | synonymous-codon | Upf1 | Mm_Celera | 8:70333392 | TGCGCTGATCATACT[A/G]ATCTGGTCATGGGTC | 19704 |
rs33105465 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70348027 | GGACCTTGCTTGGCA[C/T]ATGCTGCCCTCACCC | 19704 |
rs33119279 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Upf1 | GRCm38.p3 | 8:70355096 | TAAAAAGTGAGATTC[A/C]GGGGCTGGTGAGATG | 19704 |
rs33120689 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Upf1 | Mm_Celera | 8:70346660 | CTGGCCCCGTTCCTA[A/C]ATGTCTGGGAGCCCA | 19704 |
rs33122954 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70341985 | CACTGTCCTCTCCAG[C/T]CCAGCCCTGCTGCAG | 19704 |
rs33139978 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Upf1 | Mm_Celera | 8:70335651 | AGAGACGCAGCTGCA[C/T]ACCTGTTGAGGTAGG | 19704 |
rs33194136 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Upf1 | Mm_Celera | 8:70340162 | GGGCTGGGCTTCCCA[A/C]AGGTCAGAGCCTCTA | 19704 |
rs33232095 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70343601 | CAGAAGGCAGGTACT[C/G]TGCAACCAGAGAATG | 19704 |
rs33242330 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Upf1 | Mm_Celera | 8:70353759 | AGTCACTGCTACCCC[C/G]AGCACTCCTGAAGCC | 19704 |
rs33277630 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Upf1 | Mm_Celera | 8:70345939 | AGAAGAAGCCCTTTT[C/T]CAGAGCCACACACAA | 19704 |
rs33294821 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70346541 | CCAGTTTCTGCCTGT[C/T]TCTGCCATGAACATG | 19704 |
rs33298342 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70345246 | GGAGTGTGCTCTGCG[A/G]TCTAAAAGCTTTTAG | 19704 |
rs33327180 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70354903 | TCACAAGACAACCTA[C/T]AGGTATTGGTTCTCT | 19704 |
rs33336254 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Upf1 | Mm_Celera | 8:70336029 | CAGCAGAGAGGTGGT[A/G]TCCCCAAATATGGCT | 19704 |
rs33363588 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Upf1 | Mm_Celera | 8:70353816 | TGCGATCAAGTCGCA[C/T]TGGTCCGAGCTAGCC | 19704 |
rs33371076 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Upf1 | Mm_Celera | 8:70346933 | CCAGCCACCAAGCCA[G/T]GTCAAGAAACAGCCT | 19704 |
rs33374933 | snp | C/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70340529 | GTTTTGCTAGAGGCC[C/T]GGTCTGTTGTGCCAC | 19704 |
rs33380453 | snp | A/G | 0.475309 | 0.108333 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355968 | GTGCTTTGTTAAACT[A/G]AGGTCACAGAGGAAG | 19704 |
rs33421665 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70332755 | GTCCTGAAAGGCAAA[A/G]GTAGTGTGAACATGG | 19704 |
rs33425601 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Upf1 | Mm_Celera | 8:70334894 | GCCCAATGAAGCAAA[G/T]GCTGAGTAGGCTCCA | 19704 |
rs33436661 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Upf1 | Mm_Celera | 8:70342288 | GGTCTGTCAGCACAG[A/G]CCAGATGGTCACACC | 19704 |
rs33439945 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Upf1, Gdf1, Cers1 | Mm_Celera | 8:70331767 | CAAATCCTCCGGCTG[C/T]GGTGCAGGCGGTGAT | 19704 |
rs33443952 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70354212 | GGGAAAGGCATTCCC[C/T]CCACAGAAGTGTATC | 19704 |
rs33458087 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355280 | AATAAATCTTTTTTT[A/T]AAAAAAAAAGTGAGA | 19704 |
rs33477115 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70347578 | CAGCACCTTACACAC[A/G]ACAGGGCCAGAGCCC | 19704 |
rs33489437 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Upf1 | Mm_Celera | 8:70355355 | GCGGTGGTGGCACTC[A/G]CCTTTAATCCCAGCA | 19704 |
rs33550793 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70340911 | CAACAGCACCCCCAC[A/G]GCCCAGCACAATACT | 19704 |
rs33584908 | snp | A/T | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70349562 | ACTTTTTCCCACAGT[A/T]CTGCTCTCAGAGCCT | 19704 |
rs33604683 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70337705 | TAGGGTGGGACCTGG[A/G]ATACCCTGTTCTACA | 19704 |
rs33605909 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Upf1 | Mm_Celera | 8:70333566 | AGAGGGTAAGAAATG[A/G]CAGAAGGGTTGGTGA | 19704 |
rs33617304 | snp | A/G | 0.5 | 0 | intron-variant | Upf1 | Mm_Celera | 8:70335160 | GCCTCCAGCCAGGTC[A/G]GTAGCCCAAGGCTGA | 19704 |
rs45746825 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Upf1 | Mm_Celera | 8:70341689 | ACCTGGCCCAGGAGG[C/T]CTCAAACTAGCCAGA | 19704 |
rs45766325 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Upf1 | Mm_Celera | 8:70342921 | TCTCCAACAGTGTTT[A/C]CTGACACTTGCATGG | 19704 |
rs45813726 | snp | A/G | | | intron-variant | Upf1 | GRCm38.p3 | 8:70338665 | AGCCATGCCAAGGCA[A/G]AACAAGCAAAGCCTC | 19704 |
rs46109875 | snp | A/G | | | intron-variant | Upf1 | Mm_Celera | 8:70339676 | AAGTTGTACATATTA[A/G]AGCCCTGGGGACAGC | 19704 |
rs46220484 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Upf1 | Mm_Celera | 8:70340497 | CAAGGCCAGGAAGAG[C/T]CCCTGACTCGGGAGA | 19704 |
rs46325744 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Upf1 | Mm_Celera | 8:70349531 | AGAGGCAAGGAGAGT[C/G]TCTTTTGGTTTGCTC | 19704 |
rs46367493 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70350275 | ATAGTGGGGCCTTTC[A/G]CACAGAAAATGGGGG | 19704 |
rs46490457 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Upf1 | Mm_Celera | 8:70339547 | ACTGCTGCAGACAGA[C/T]TCCAGGCTGTTTCAC | 19704 |
rs47467917 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Upf1 | Mm_Celera | 8:70341016 | ATCCTGTAGCAACAT[A/G]CCTCCTCTGGGACCA | 19704 |
rs47473357 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Upf1 | Mm_Celera | 8:70345733 | CCACATGGCCACTAA[A/T]GAAACCTTTCTCAGC | 19704 |
rs47686713 | snp | A/C | | | intron-variant | Upf1 | Mm_Celera | 8:70348777 | CAAGGCTGTGCAGAG[A/C]TGGAACAGACCGACT | 19704 |
rs47936826 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Upf1 | Mm_Celera | 8:70348665 | CACAGCTAACTCCAT[G/T]GGCAGGGACACACAG | 19704 |
rs47937142 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70345335 | TGGGCCTCATATGTA[C/T]CAGGCAGGAGTTTTA | 19704 |
rs48412309 | snp | A/G | 0.396694 | 0.202437 | synonymous-codon | Upf1 | Mm_Celera | 8:70334689 | CTGATGTTCATTGGC[A/G]CGCACGCAGGACAGA | 19704 |
rs48433096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70347818 | TCTCGAGTGAATCAC[A/G]GCTAAAATGGTTGCC | 19704 |
rs48568823 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Upf1 | GRCm38.p3 | 8:70345737 | ATGGCCACTAAAGAA[A/G]CCTTTCTCAGCAGGG | 19704 |
rs48769136 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70345197 | CTGGCTGCAATCATC[C/T]GGGGTCTGTACTGAT | 19704 |
rs48884701 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Upf1 | Mm_Celera | 8:70334611 | GTAGTGATGGGCAGC[A/G]GCCTACCTTGCTCTG | 19704 |
rs49162560 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70345599 | TCTTTAAAACTTTGA[C/G]GAAAGATACAGAGCA | 19704 |
rs49201847 | snp | A/G | 0.18 | 0.24 | intron-variant | Upf1 | Mm_Celera | 8:70346921 | CTGAGCTGTAAACCA[A/G]CCACCAAGCCAGGTC | 19704 |
rs49302176 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Upf1 | Mm_Celera | 8:70342583 | ACCCCAATAGTGGCC[C/T]ACATTGGCTGGCCAC | 19704 |
rs49937060 | snp | C/T | 0.124444 | 0.216185 | intron-variant, synonymous-codon, utr-variant-3-prime, downstream-variant-500B | Upf1, Gdf1, Cers1 | Mm_Celera | 8:70331162 | GGGCACTTGTCGTAC[C/T]CGACGGTTGCATGTG | 19704 |
rs50207422 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70349817 | AGTCTCCAGTAAGGG[C/T]ACACAGTGGCATCTG | 19704 |
rs50382479 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Upf1 | Mm_Celera | 8:70339505 | CTTCATCACTAGACC[A/G]GCTCTCCTTGCCTAT | 19704 |
rs50401008 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Upf1 | Mm_Celera | 8:70349022 | TGCCACCCTCTGTCA[A/G]TTCTCCTCTCAGCCT | 19704 |
rs50411109 | snp | C/T | | | intron-variant | Upf1 | Mm_Celera | 8:70351642 | TGCAGCTCCCCCCCC[C/T]CCCCGAGAGAATACA | 19704 |
rs51038735 | snp | C/T | | | utr-variant-5-prime | Upf1 | Mm_Celera | 8:70353078 | GGCCGTAATCCGGAG[C/T]AGCCGCTGCCGCCGC | 19704 |
rs51392256 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Upf1 | Mm_Celera | 8:70353324 | CGGACGCCGGCACAG[A/G]TGCGCGTGCGCGAGT | 19704 |
rs51498623 | snp | A/C/G | | | intron-variant | Upf1 | GRCm38.p3 | 8:70351647 | CTCCCCCCCCTCCCC[A/C/G]AGAGAATACAGGAAA | 19704 |
rs51654086 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Upf1 | Mm_Celera | 8:70335888 | AAGACATGGCTGCCT[A/G]CTGAGTACACGAGGA | 19704 |
rs51898848 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Upf1 | Mm_Celera | 8:70346103 | TGCTAGATGGACCCT[A/T]CCTAAGGTTCACCAC | 19704 |
rs52025671 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Upf1 | Mm_Celera | 8:70344022 | CTCTTTAAGCCTCCA[A/G]TGCCCTCATGTGGCC | 19704 |
rs52145518 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Upf1, Gdf1, Cers1 | Mm_Celera | 8:70332012 | aaagaaaaaaaaaag[A/G]aaaaCCAGAAAAACC | 19704 |
rs211725443 | snp | G/T | | | intron-variant | Upf1 | Mm_Celera | 8:70352043 | GAACCCTGGCTGGAG[G/T]GGGTGGTGGATGAAG | 19704 |
rs211828383 | snp | A/G | | | intron-variant | Upf1 | Mm_Celera | 8:70350686 | TGGTGGCTGAAGAGA[A/G]GCTGAGGGTGCAGGG | 19704 |
rs212498576 | snp | C/T | | | intron-variant | Upf1 | Mm_Celera | 8:70336661 | ACCTCAGAAGACAAG[C/T]TCTCATAATCTACCT | 19704 |