SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6168282 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rev1 | Mm_Celera | 1:38083453 | AAGTAGACTAATCAC[C/T]GTTTTAAAAATCATA | 56210 |
rs6179217 | snp | A/G | 0.304688 | 0.243945 | intron-variant, upstream-variant-2KB | Rev1 | Mm_Celera | 1:38089672 | TTTTTGGTAATGATG[A/G]TCTGACTACATAGAA | 56210 |
rs6275057 | snp | C/T | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062494 | ctgggagtaaagctg[C/T]ctctaggatcctgag | 56210 |
rs6287919 | snp | A/T | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062664 | tgtgccattggtcag[A/T]tggggttcccaagtn | 56210 |
rs6288324 | snp | A/C | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062679 | ntggggttcccaagt[A/C]cctggatcccactgg | 56210 |
rs6288375 | snp | A/G | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062709 | gtcccagttattccc[A/G]gtggagttgggacag | 56210 |
rs6288844 | snp | A/G | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062781 | taagagagcctgaga[A/G]tggagcttcctccag | 56210 |
rs6289423 | snp | A/T | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062906 | TGTTTGGCCTTTTTC[A/T]CTTCANTGGTAATGA | 56210 |
rs6289437 | snp | C/T | 0.5 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38062912 | GCCTTTTTCNCTTCA[C/T]TGGTAATGAGAATAA | 56210 |
rs6354514 | snp | C/T | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Rev1 | Mm_Celera | 1:38085450 | AAGAAAGGAACTGAT[C/T]TGACCAAGGAAAATC | 56210 |
rs6355079 | snp | A/G | 0.484429 | 0.0868505 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | Rev1 | GRCm38.p3 | 1:38085549 | GGAATACAGACCTTT[A/G]AGATCNGGTCTATTT | 56210 |
rs6355082 | snp | A/T | 0.5 | 0 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | Rev1 | Mm_Celera | 1:38085555 | CAGACCTTTNAGATC[A/T]GGTCTATTTCGTATA | 56210 |
rs30476855 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rev1 | GRCm38.p3 | 1:38128513 | CAAAGCCCGGTCAAT[A/G]TGGGAAAGCAAACTT | 56210 |
rs30888607 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38127955 | ACTAGCAGAGGCAAA[A/T]TTCAAGCCCATATGT | 56210 |
rs30962563 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38061421 | TAGGCTGGCATTTGT[A/G]TTCTCTTAGGGTCTG | 56210 |
rs30966163 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rev1 | Mm_Celera | 1:38070485 | GTTGAGTAAAACAAG[C/T]ACACAATAAGCCACG | 56210 |
rs30967937 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38122843 | GGTCTGGCCTTAAAT[G/T]CACTAGGTAGCTGAG | 56210 |
rs31061586 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Rev1 | GRCm38.p3 | 1:38096797 | TAAAAACATGTACTA[A/G]TGTTGCAGAGGATCT | 56210 |
rs31092127 | snp | C/T | 0.498615 | 0.0262793 | intron-variant, upstream-variant-2KB | Rev1 | Mm_Celera | 1:38081640 | ATAAGGAACAAGAAA[C/T]CAGTCTCTAAAAAAG | 56210 |
rs31162453 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Rev1 | GRCm38.p3 | 1:38064074 | AATCACTAAGCACAG[A/G/T]GCCACACATGGCAGT | 56210 |
rs31177160 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rev1 | GRCm38.p3 | 1:38086092 | ACATAGAGGTTTACA[A/G]GGGTTAATTTAGATT | 56210 |
rs31190496 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38117286 | GGGCATAGTGGTGCA[C/T]GCCTTTAATCCCAGC | 56210 |
rs31284028 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38123505 | ACATTAAAAAAAAAA[C/T]AAAAAAAAAAAAAAC | 56210 |
rs31378342 | snp | A/G | 0.455 | 0.143091 | intron-variant | Rev1 | GRCm38.p3 | 1:38124855 | TAACTCCTTCCTGGT[A/G]TCAATTTTCTAAGGA | 56210 |
rs31382336 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Rev1 | GRCm38.p3 | 1:38128287 | CATGACAAGATACAC[A/G]ATTTTGGTACATACT | 56210 |
rs31441066 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rev1 | Mm_Celera | 1:38129366 | GGCAGCACCGCGAGC[C/T]CCCGGCCTCGGCGCC | 56210 |
rs31461552 | snp | G/T | 0.455 | 0.143091 | intron-variant | Rev1 | GRCm38.p3 | 1:38124958 | GATGGTCTCTTTTGA[G/T]AAGTCCAGACTTCCT | 56210 |
rs31474512 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rev1 | Mm_Celera | 1:38124085 | AGACTTTTTTTTGTC[C/T]ACCCCTACTCACATG | 56210 |
rs31523873 | snp | A/G | 0.455 | 0.143091 | intron-variant | Rev1 | GRCm38.p3 | 1:38068574 | AGGGGTGAAAAGGCA[A/G]GCAGACAGTAACTGT | 56210 |
rs31551087 | snp | A/G | 0.5 | 0 | intron-variant | Rev1 | GRCm38.p3 | 1:38069222 | ACTACTGGCAGTCAG[A/G]GGAAGTAATTTATTT | 56210 |
rs31552424 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rev1 | Mm_Celera | 1:38120625 | CTCAATATTGTTTGC[A/G]CTGGATCCACAGTCT | 56210 |
rs31571516 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rev1 | GRCm38.p3 | 1:38122151 | ACAAGGCAAATGAGC[A/G]TCAGTGAGATGCAAC | 56210 |
rs31603128 | snp | C/T | 0.5 | 0 | intron-variant | Rev1 | GRCm38.p3 | 1:38068297 | GTATGATAGAAATAA[C/T]AAATATAAATTCTTA | 56210 |
rs31645005 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38065420 | AAAAAAAAAAGAAAA[A/G]AAAAGAAAAAAAGAA | 56210 |
rs31652262 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Rev1 | GRCm38.p3 | 1:38110930 | AGAGAGGAGGGCAAT[G/T]GATCAGGATACAAAT | 56210 |
rs31712736 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38062187 | CTCTGTCATCATCGT[A/G]AGAAGTGATTTTAGA | 56210 |
rs31724351 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38120868 | AGAAGAAAGCCTCCA[C/T]TAAGGAACTACCTAG | 56210 |
rs31726365 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Rev1 | GRCm38.p3 | 1:38067115 | GCTAGGTTTATAAAT[C/T]TGGTACTGGGAATGG | 56210 |
rs31764214 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38097963 | TTATGTGCAACCTGT[A/T]CAAGGCCTTAGGTTC | 56210 |
rs31829309 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rev1 | GRCm38.p3 | 1:38093271 | CATTTGGAGGTGTGG[C/T]CTTGTTGGAATAGGT | 56210 |
rs31839882 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38097130 | ACTTTCAATCTTCTT[C/T]GAGCCAAGGTCTCCT | 56210 |
rs31855281 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38123513 | AAAAAAATAAAAAAA[A/C]AAAAAACATTTGACT | 56210 |
rs31922085 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rev1 | Mm_Celera | 1:38125776 | AGAGACCAAAAGGTA[A/G]GGTTGTAGAATATCA | 56210 |
rs31922174 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38061773 | AGTATCCTTATGTTC[C/G]GTCTTCTCATTGTGT | 56210 |
rs31964055 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38127707 | CCTCAGGATCTGTTC[A/T]CTAGTAGACAGCAGG | 56210 |
rs31978443 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Rev1, LOC105243909 | Mm_Celera | 1:38072956 | CAGCTTTCAGCTTAG[C/T]GTTTTACAGGGCCCC | 56210 |
rs32014742 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38061629 | TGGTCCAGTCTATTT[C/G]GAGTTCTGTAGGCTT | 56210 |
rs32015215 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rev1, LOC105243909 | GRCm38.p3 | 1:38074095 | TAGTCCGGTAGATCT[C/T]ACAATATGCAGTAGC | 56210 |
rs32019002 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38126680 | GGCCTCTACACACAG[C/T]ACAGGAAACTCAGAC | 56210 |
rs32034900 | snp | C/T | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Rev1 | GRCm38.p3 | 1:38089119 | TGTAACACATTAAAC[C/T]CAATACCACAGCACA | 56210 |
rs32042915 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rev1 | GRCm38.p3 | 1:38058658 | ATGTGATCTGTTCAC[A/G]GTCATGCTGGTGTCA | 56210 |
rs32047224 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rev1 | GRCm38.p3 | 1:38096163 | AGTAATAAGACATTA[C/T]TGAACTTTTAGAATT | 56210 |
rs32067118 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38102246 | TTTTTTGTAACTTTT[A/T]AAAAAAACAATTGCT | 56210 |
rs32074491 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38127704 | AGCCCTCAGGATCTG[C/T]TCTCTAGTAGACAGC | 56210 |
rs32099635 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rev1 | GRCm38.p3 | 1:38121977 | CAAAAAGTACAGAGA[C/T]GCTTAAGGCAACATT | 56210 |
rs32123034 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Rev1 | GRCm38.p3 | 1:38063872 | GAGTTCATAACGGAA[A/C]GTCGTCTGCATAAAA | 56210 |
rs32123134 | snp | A/T | 0 | 0 | intron-variant | Rev1 | Mm_Celera | 1:38109200 | AAGGACAAAGAATTC[A/T]CTAAATGAATTCTTA | 56210 |
rs32147336 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38127893 | ATTTATTAGTCGGCT[A/G]CCCAAACTGGAAAAT | 56210 |
rs32158678 | snp | A/G | 0.401235 | 0.199068 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rev1, Eif5b | GRCm38.p3 | 1:38053816 | TCAGGTCCTGTTCTC[A/G]AATCACAGAGCTACC | 56210 |
rs32220312 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rev1 | GRCm38.p3 | 1:38068349 | AGCCGTATCAAAATT[A/G]TAGAAGTGGTAAGTC | 56210 |
rs32275788 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38106565 | TAAATGAAGATAACC[A/G]ATTCCTACAAACTGT | 56210 |
rs32278730 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rev1, Gm5099 | Mm_Celera | 1:38131828 | TAAAATTGATTTTTT[A/T]AAAAAATTTAATCAT | 56210 |
rs32288413 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38062629 | TATGCTCAGGGTTCC[A/G/T]GCCCAGACAGGAAGG | 56210 |
rs32305789 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rev1, Gm5099 | Mm_Celera | 1:38130844 | TCCCAGCTCTGTTTC[C/T]CTGGACCCACAATTG | 56210 |
rs32354258 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38114626 | CCACTCTCTCCCTAT[C/T]AACACAATACTTGAA | 56210 |
rs32360111 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rev1 | GRCm38.p3 | 1:38120672 | CTATGTACTAATAAA[C/T]TTAAGAACACTTAAA | 56210 |
rs32374333 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Rev1 | GRCm38.p3 | 1:38123487 | CAACTTACAACAGAA[G/T]CTACATTAAAAAAAA | 56210 |
rs32436956 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rev1 | GRCm38.p3 | 1:38128524 | CAATATGGGAAAGCA[A/G]ACTTATGGAGTCTTG | 56210 |
rs32457741 | snp | A/G/T | 0.465374 | 0.126941 | intron-variant, utr-variant-3-prime | Rev1, Eif5b | GRCm38.p3 | 1:38055108 | TCATGATCTGTGTGA[A/G/T]CCAGTAAAGTCAACA | 56210 |
rs32468069 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38099563 | TGGTTTATTTTGAGG[C/T]AAGGTTTCTCTGTGT | 56210 |
rs32516403 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Rev1 | GRCm38.p3 | 1:38106760 | AAAACTTAGATGACA[C/G]TAGAGCAGTGGTTCT | 56210 |
rs32539479 | snp | A/G | 0.32 | 0.24 | intron-variant | Rev1 | GRCm38.p3 | 1:38128137 | AAGAAGTGGAGTTAC[A/G]TATTTCAGCACATTA | 56210 |
rs32578944 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rev1 | GRCm38.p3 | 1:38123012 | AGAACATTGTCTATT[A/G]GGAGTAATGGACTTG | 56210 |
rs32599800 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rev1 | GRCm38.p3 | 1:38121178 | ACAGTAAAGTTTGAA[A/G]CCACAGGATTTCATG | 56210 |
rs32607026 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rev1 | GRCm38.p3 | 1:38122013 | ATTAACTGAGAAGTA[A/G]GTCCCATGGTCAGCT | 56210 |
rs32649168 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38122366 | AATCTCTGCAGCTCA[A/C]TGGGCAATGACAGCC | 56210 |
rs32651277 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rev1 | Mm_Celera | 1:38058167 | ATTTCTACATAAAGT[A/G]TGTTGTTTTACTTCT | 56210 |
rs32699229 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Rev1 | GRCm38.p3 | 1:38125067 | TCCATGTTTAAATGG[A/G]TATTAAATTCTTCAT | 56210 |
rs32718735 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rev1 | Mm_Celera | 1:38125242 | ATACTCTTGCAAACA[A/T]ATGACAACAATGAAA | 56210 |
rs32724012 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rev1 | GRCm38.p3 | 1:38125380 | TTTCTTCCTAAGTGT[A/G]CCAATTTTATACAGT | 56210 |
rs32726701 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Rev1 | GRCm38.p3 | 1:38123262 | ACAACTGAGTATTTT[A/T]AAAACCAGAAAAGTG | 56210 |
rs32742760 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38096931 | TTGACCTTTTTATGT[A/G]TGCTATGGCACATGT | 56210 |
rs32748858 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rev1 | GRCm38.p3 | 1:38061572 | TCTTTGTTTAGTGCA[G/T]TTGGTGTCTTGATTA | 56210 |
rs32768215 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rev1 | GRCm38.p3 | 1:38127888 | AACTAATTTATTAGT[C/T]GGCTACCCAAACTGG | 56210 |
rs32969518 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rev1, Eif5b | Mm_Celera | 1:38052334 | TGCCCTCAGAGGGGC[A/G]CTCTGCATACATTCC | 56210 |
rs32969521 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, utr-variant-3-prime | Rev1, Eif5b | GRCm38.p3 | 1:38053138 | TAAAACCACCTGAAC[A/G]TTGTCAAGAATAAAG | 56210 |
rs32970295 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon | Rev1 | GRCm38.p3 | 1:38057764 | ATCTGTTGCCTGGTC[A/C]AGAGTTACAGTCCTG | 56210 |
rs32970298 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rev1 | Mm_Celera | 1:38058054 | GAATTAAAACAGACT[G/T]CATGGTAGAAAGCCA | 56210 |
rs32970303 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rev1 | Mm_Celera | 1:38058351 | CTGGCTTGTCAGAGT[A/G]CAATTTGCTGAACAA | 56210 |
rs32970486 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B | Rev1, Eif5b | Mm_Celera | 1:38053943 | ACAGCTGCTCTGGCC[C/T]GGCAGTAAACTAGAT | 56210 |
rs32970489 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rev1, Eif5b | Mm_Celera | 1:38054307 | GGCACTAAAAGAGGA[A/G]GTATGAGAGTCTCAA | 56210 |
rs32970492 | snp | A/C | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rev1, Eif5b | Mm_Celera | 1:38054452 | TCAGCTGTACAACTT[A/C]GTATTCTCATTTAGC | 56210 |
rs32970984 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Rev1 | GRCm38.p3 | 1:38067591 | CTTTGCTTTCTTAGT[C/T]GCCATTCTAGCAAGA | 56210 |
rs32970987 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rev1 | Mm_Celera | 1:38067627 | ATTAGAACCTGTGAC[A/G]TTGAGAACAAAAGAA | 56210 |
rs32970990 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rev1 | Mm_Celera | 1:38067799 | TAGTTTTTCAGAATA[C/T]GGCCAGAATGGTTGC | 56210 |
rs32971056 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rev1 | Mm_Celera | 1:38058618 | ACCCGAGGAAGCCTC[A/G]GGCTGCCACCTGGCT | 56210 |
rs32971060 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rev1 | Mm_Celera | 1:38058981 | TGACCATGGGCTGTG[C/G]CTGCCTCTACAGGCT | 56210 |
rs32971063 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rev1 | Mm_Celera | 1:38059344 | CTTTTCCTTAACCTA[A/G]TAGGTTCTTCTCAAG | 56210 |
rs32971254 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rev1, Eif5b | Mm_Celera | 1:38054469 | TATTCTCATTTAGCA[A/G]TTACGTAGGTTTAAT | 56210 |
rs32971257 | snp | A/T | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Rev1, Eif5b | Mm_Celera | 1:38054516 | GACTCATGTTTTGAG[A/T]TTTCATGTTTTGAAC | 56210 |