SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3713635 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Exoc5 | Mm_Celera | 14:49039884 | CGCCATCCTGGTCTA[C/T]AGAGTGAGTTCCAGG | 105504 |
rs4137184 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Exoc5 | Mm_Celera | 14:49040078 | ATTCAATGATGAGCC[C/T]ATGAGAATAACCATC | 105504 |
rs13459143 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Exoc5 | GRCm38.p3 | 14:49014179 | TAGATCTGCCCGCCT[A/G]GCGCGACACTTCAGC | 105504 |
rs13459611 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime | Exoc5 | GRCm38.p3 | 14:49013116 | ATTCTCCAGTCTCAA[A/G]GCATTTCTGAAGTTA | 105504 |
rs30110761 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49067916 | ACCCCCATTAGTTGT[A/T]AGTTTTGCTTACATT | 105504 |
rs30125391 | snp | A/G | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49039653 | AGGAAATTTACATGG[A/G]ATAACCAATTCCTTT | 105504 |
rs30139075 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Exoc5 | Mm_Celera | 14:49014430 | TCTTCTCACATCTTG[C/T]TAGTCAGAACTTAAT | 105504 |
rs30147787 | snp | C/G | 0.493827 | 0.0552116 | utr-variant-3-prime | Exoc5 | Mm_Celera | 14:49014117 | TGTGCTTCCCATTAC[C/G]GAGGCCTTCTGAGAA | 105504 |
rs30216002 | snp | A/G | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49028924 | GGTTCTAAAAGCAAA[A/G]CAAAACAAACAAACA | 105504 |
rs30241964 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Exoc5 | Mm_Celera | 14:49033441 | ACCATAAAAACAAAT[A/G]AAAAAAGTGGTTACT | 105504 |
rs30275012 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068651 | TTATGTAAACTCTCT[C/G]TCTTTTATTGACTCA | 105504 |
rs30341383 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ap5m1, Exoc5 | Mm_Celera | 14:49065318 | TTCAGTAACAAAAAA[A/G]AGTAACTGAAAAGTT | 105504 |
rs30350961 | snp | A/T | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49062797 | ATAAACTAACTCCTC[A/T]GTAACCAAATTCTCT | 105504 |
rs30361447 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Exoc5 | Mm_Celera | 14:49024110 | GACTTCTTGGATTTT[G/T]AAATATTTACAAATT | 105504 |
rs30382006 | snp | C/G | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49055376 | AGACTATGTTAACTA[C/G]TTTAAACAGTAAAAC | 105504 |
rs30382148 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49033714 | CTTCACCACCGTTCC[A/G]TTAGTCAGGGTCTTT | 105504 |
rs30502368 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49045281 | TTGTGAGACTATGCC[A/G]GGGCCTAGCAAACAC | 105504 |
rs30507489 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Exoc5 | Mm_Celera | 14:49024354 | AACAATATAAGCCTG[A/G]TGTTTAAAGTACATT | 105504 |
rs30512762 | snp | A/C | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49042882 | TAAGTTTATAAAATT[A/C]AAACAGAATAGACAA | 105504 |
rs30554172 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Ap5m1, Exoc5 | Mm_Celera | 14:49065753 | TCCACAGCAATTAAA[C/T]GCAGTAAGATGTGTC | 105504 |
rs30566385 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49067563 | TTGATTTCAGGAGAT[A/C]CCATCTGTCAGTTCT | 105504 |
rs30588719 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Exoc5 | Mm_Celera | 14:49027593 | GGAGCCTTTATACCC[G/T]TGTGTACAAGGCGGA | 105504 |
rs30602065 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Exoc5 | GRCm38.p3 | 14:49026898 | GGAGTCTTCACCCAG[A/C]AACTGATGGAAACTA | 105504 |
rs30618274 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068616 | TTCTTCTTTATATGA[C/T]TTGAGTTTTCCTAAC | 105504 |
rs30620908 | snp | A/C | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49030766 | GGCTTCAGCCCTCCA[A/C]AAAGGACTACAGGCA | 105504 |
rs30651171 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Exoc5 | Mm_Celera | 14:49037638 | AATCTTCAGAACCTC[A/G]AAGCTGATCATAAGT | 105504 |
rs30686276 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Exoc5 | Mm_Celera | 14:49017401 | ATCAACTCTAAAAAC[C/T]CTGTTCATGCTGCTA | 105504 |
rs30748919 | snp | C/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49055710 | CAGAGATCCCCTCAG[C/G]TGCTGAGGGGCATTT | 105504 |
rs30749387 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Exoc5 | Mm_Celera | 14:49064078 | ATCCCGTCAACTGAG[G/T]AAAGATTTACAGTTT | 105504 |
rs30764271 | snp | C/T | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49021560 | AATCCTTTACCCTGC[C/T]TCCCCGTTAGTATTT | 105504 |
rs30783384 | snp | A/C | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49043274 | CATAAAAGAAGGACT[A/C]AGACTATTAGTATAG | 105504 |
rs30826500 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49017960 | CCAACTAATAATATG[A/G]ACAGTAGAAAGTAAA | 105504 |
rs30841374 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068243 | GAGGTCCTGAGTTCA[A/G]TTCTCAGCAACCACA | 105504 |
rs30848324 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Exoc5 | Mm_Celera | 14:49024269 | TCCCATTGTACTAGT[A/G]GTCAAAAATTTTTTA | 105504 |
rs30860205 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Exoc5 | Mm_Celera | 14:49051125 | CAACGCCAACGCCAA[C/T]GCCAACACCAACGCC | 105504 |
rs30870297 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Exoc5 | Mm_Celera | 14:49043315 | GCGCTTATGTTAACC[A/C]TGGCAGGGCTTTCTC | 105504 |
rs30896113 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068258 | ATTCTCAGCAACCAC[A/G]TGGTGGCTCAAAACC | 105504 |
rs30918497 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068293 | GTAATGTGATCTGAT[A/G]CCCTCTTCTGGTGTG | 105504 |
rs30939131 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49068158 | CCCTGAATGCAAACA[C/G]AGTCATTAGAAATCA | 105504 |
rs30944783 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Exoc5 | Mm_Celera | 14:49055838 | TGGCAGGTCATTTTA[A/C]TTTTGTAACTTTTCA | 105504 |
rs30994660 | snp | A/G | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49050388 | CACATTAGCAGAAAC[A/G]AGCTTACTAGTTCCA | 105504 |
rs30998898 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | GRCm38.p3 | 14:49042618 | TTTAAGAGTATAGCT[A/G]AAAAGATTAATACCT | 105504 |
rs31021821 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Exoc5 | Mm_Celera | 14:49031475 | AGTTCAGGCCTAGTA[A/C]TGTGAACTTGGTCAA | 105504 |
rs31035559 | snp | A/C | 0 | 0 | intron-variant | Exoc5 | Mm_Celera | 14:49022508 | AACCTAAGAGAAGAT[A/C]ACTGTTGGAGGAATA | 105504 |
rs31047175 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Ap5m1, Exoc5 | Mm_Celera | 14:49065822 | TCCTTAAAAGAATCC[A/T]CCCAGCCTTTTCGAC | 105504 |
rs31048643 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Exoc5 | Mm_Celera | 14:49022878 | CAAAACTTCATTACT[C/T]AATTCCTAAGCAGAA | 105504 |
rs31056604 | snp | A/G | 0.426035 | 0.177515 | intron-variant, downstream-variant-500B | Exoc5 | GRCm38.p3 | 14:49019309 | CAAACCTCCTGTCCT[A/G]TTTGATGCTTATATG | 105504 |
rs31069159 | snp | G/T | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49038962 | CTGTTTTTTGTTTTT[G/T]TTTTTTTTTTTTTTA | 105504 |
rs31100985 | snp | C/T | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49029074 | ATAAACAAAGCAACC[C/T]AAAACTCTATTCTGT | 105504 |
rs31310185 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49017350 | GATTTCCAGGGGGGG[A/G]AAATTCTCTTATAGA | 105504 |
rs31335953 | snp | C/T | 0.5 | 0 | intron-variant | Exoc5 | Mm_Celera | 14:49017198 | AGGGCTTCCCACATG[C/T]TAGCAATACTCTACC | 105504 |
rs31390012 | snp | A/G | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49015998 | CAAGGAAGCAGGAAC[A/G]GTGTTTAGACAGTGG | 105504 |
rs31431428 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49067644 | ATGAGTAGATGTGTG[A/T]TCTTGGAAAGCAGCA | 105504 |
rs31505775 | snp | C/T | 0.5 | 0 | intron-variant | Exoc5 | Mm_Celera | 14:49037548 | AAATATTAAATAACA[C/T]TTAACAACATCAATA | 105504 |
rs31529209 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Exoc5 | Mm_Celera | 14:49024236 | AAACTTTAAGGCCAT[A/G]AGTAGAACTTTCCAA | 105504 |
rs31530453 | snp | A/T | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49030637 | GATTTCAAGTTTGCT[A/T]TGAGAGTATGTCTCC | 105504 |
rs33884871 | snp | C/T | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49047728 | ATTTTGTTTGGAGCA[C/T]ATGACCCAACAGGTA | 105504 |
rs45712887 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49016153 | CAGGTGCACTAATGC[A/G]TGTACAAGAATGAAG | 105504 |
rs45873300 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Exoc5 | Mm_Celera | 14:49053353 | AAGGTCCAATCAAAC[A/G]AGCAAATATGCATGT | 105504 |
rs46026959 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49045497 | TCACTGGAAAGAGAG[A/G]CCCATTGGACAGGCA | 105504 |
rs46055188 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49043576 | GCTCTTACTCCTTTC[A/G]GGAAGTGTGCTTGAT | 105504 |
rs46127406 | snp | A/C | 0.5 | 0 | intron-variant | Exoc5 | Mm_Celera | 14:49037888 | AGTGGTTATGGGTCT[A/C]TCTTCTTTTGGAAGA | 105504 |
rs46154637 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Exoc5 | Mm_Celera | 14:49013344 | GTTATTTCTCACATA[C/T]ACCGTTTACACTATA | 105504 |
rs46165068 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Exoc5 | Mm_Celera | 14:49018720 | GACTACCTCCTGATT[A/T]GCTTGCATAACTTAA | 105504 |
rs46231903 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Exoc5 | Mm_Celera | 14:49034465 | ACAGCTCAACCCAGG[A/G]CTGCTGAAAGTGTAA | 105504 |
rs46428825 | snp | A/C | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49042043 | ATTTAAAAGGGCATT[A/C]TTAACTTAAATTCTC | 105504 |
rs46470986 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Exoc5 | Mm_Celera | 14:49051371 | AAACTCTTTAGCTTC[C/T]TTCTGACACTGTTGT | 105504 |
rs46553556 | snp | A/G | 0.260355 | 0.249785 | intron-variant, missense | Exoc5 | Mm_Celera | 14:49019549 | AGGCATAGGTAAGTG[A/G]GAACAACCTTTAAAA | 105504 |
rs46718594 | snp | C/T | | | intron-variant | Exoc5 | Mm_Celera | 14:49051502 | GCACAACCAACTTGC[C/T]TGCCAGTAACCATAA | 105504 |
rs46722085 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ap5m1, Exoc5 | Mm_Celera | 14:49065688 | AATGCACCTGAACGC[C/T]CCCACAGCTTCTCAC | 105504 |
rs46793721 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Exoc5 | Mm_Celera | 14:49061144 | AAAATCCTTCTCAGA[C/T]TGCAAAAATGGATCT | 105504 |
rs46928721 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Exoc5 | Mm_Celera | 14:49061955 | ACTCACACTCTTCCT[A/G]TTCTGCAACCCCAAT | 105504 |
rs46995323 | snp | A/G | 0.42 | 0.183303 | intron-variant | Exoc5 | Mm_Celera | 14:49048219 | GTAAATTTGGATTAA[A/G]ACTGTATTCAAGACG | 105504 |
rs47075174 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Exoc5 | Mm_Celera | 14:49027592 | TGGAGCCTTTATACC[C/T]GTGTGTACAAGGCGG | 105504 |
rs47155710 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon, nc-transcript-variant | Exoc5 | Mm_Celera | 14:49051383 | TTCCTTCTGACACTG[C/T]TGTTCTAATTTCTCC | 105504 |
rs47192451 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Exoc5 | Mm_Celera | 14:49061148 | TCCTTCTCAGATTGC[A/G]AAAATGGATCTCAAA | 105504 |
rs47225678 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Exoc5 | Mm_Celera | 14:49020176 | ATTGTTGGTAGGAAA[A/G]TTAAAGGTGCCAACA | 105504 |
rs47253829 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Exoc5 | Mm_Celera | 14:49012549 | GTACGTTCTAAGTGG[C/T]AACAGTACAAGCACA | 105504 |
rs47266735 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49016363 | CTCAATTTTACCTAC[A/G]GATTATACGGAATTA | 105504 |
rs47349454 | snp | G/T | 0.375 | 0.216506 | intron-variant | Exoc5 | Mm_Celera | 14:49049037 | ACAATAACAAAACTT[G/T]TATAAGAGGACCACA | 105504 |
rs47466795 | snp | C/T | | | splice-acceptor-variant | Exoc5 | Mm_Celera | 14:49051468 | AATTCTTCTAATAAC[C/T]TAATAGAGGAAAATA | 105504 |
rs47475056 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Exoc5 | Mm_Celera | 14:49051362 | CTTCTTAGCAAACTC[C/T]TTAGCTTCTTTCTGA | 105504 |
rs47488522 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Exoc5 | Mm_Celera | 14:49028204 | CAGGGACAGTGACAA[C/T]GGTCTTAGTGAAAAT | 105504 |
rs47603691 | snp | C/T | | | missense, nc-transcript-variant | Exoc5 | Mm_Celera | 14:49051414 | ACTTTCCTTTGAATC[C/T]TTTCATCCATTATCT | 105504 |
rs47606222 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Exoc5 | Mm_Celera | 14:49037433 | TACAAGTATTTCTGA[C/G]TGAAAATGGTACATT | 105504 |
rs47755109 | snp | G/T | | | intron-variant | Exoc5 | Mm_Celera | 14:49043853 | ATGTGAGAGTAAGGT[G/T]TAGCTCAATCTGTAG | 105504 |
rs48183457 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Exoc5 | Mm_Celera | 14:49061752 | ACAAGAAAGAGTGTT[A/G]GAGGGTGACAAATCT | 105504 |
rs48283229 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Ap5m1, Exoc5 | Mm_Celera | 14:49066608 | TGAGGAGTGTTTTAA[C/T]CTCTTGAAGGGACCG | 105504 |
rs48306388 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49043870 | AGCTCAATCTGTAGA[A/G]CGTTTGCTTAGCAGG | 105504 |
rs48312658 | snp | C/T | | | intron-variant | Exoc5 | Mm_Celera | 14:49051297 | TAGTCTATTAAACTC[C/T]TCGTTCTTAGCCAAA | 105504 |
rs48334393 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Exoc5 | Mm_Celera | 14:49028147 | AACCAGAGAGTTGGT[A/T]AAAAAAAAAATCTCT | 105504 |
rs48532548 | snp | C/T | | | intron-variant | Exoc5 | Mm_Celera | 14:49053628 | GGCTGGAAAGATGGG[C/T]CAGTGGTTAAGAGCA | 105504 |
rs48598080 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Exoc5 | Mm_Celera | 14:49043656 | AATCCTCAGTGCTAA[C/T]TGTTTGGTAAGAGTT | 105504 |
rs48721542 | snp | A/G | | | intron-variant | Exoc5 | Mm_Celera | 14:49053502 | GATATCACATTGGAA[A/G]CTGATGCTTATCAGC | 105504 |
rs48753165 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Exoc5 | Mm_Celera | 14:49045785 | CATTTCATCTACTTC[A/G]AATTCCTCCTACAGT | 105504 |
rs48778047 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Exoc5 | Mm_Celera | 14:49023937 | TTTACTTTGGTGTTG[C/T]TACCATTAGACTATT | 105504 |
rs49010030 | snp | C/T | | | intron-variant | Exoc5 | GRCm38.p3 | 14:49045819 | ATCTCCCTAGAGCTA[C/T]GTGGGTGATTTCCCT | 105504 |
rs49162825 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Exoc5 | Mm_Celera | 14:49023797 | GTCTTTAGAAGGTTA[C/T]TCAATTTCACCAAGT | 105504 |
rs49386570 | snp | A/G | 0.32 | 0.24 | intron-variant | Exoc5 | Mm_Celera | 14:49016717 | AGGCACTGGTTAAAA[A/G]GTACCAATAATATCT | 105504 |
rs49605355 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime | Exoc5 | Mm_Celera | 14:49014121 | CTTCCCATTACCGAG[A/G]CCTTCTGAGAAAACA | 105504 |