| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3719516 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Eps15 | Mm_Celera | 4:109286975 | CTTAGTTTAAATAAC[G/T]TAGTCAATAAGATGA | 13858 |
| rs3720093 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eps15 | Mm_Celera | 4:109287056 | ATATTTTACATGTTC[A/G]TGTGCCTGTAGTTAC | 13858 |
| rs6187227 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Eps15 | Mm_Celera | 4:109379708 | TGTGGGAGAACCAAC[G/T]CGGACAGACCAAGCT | 13858 |
| rs6187322 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Eps15 | Mm_Celera | 4:109379756 | TGAATGTAAAGGTTA[A/G]AGTGTCACTTCTAAG | 13858 |
| rs6188325 | snp | A/G | 0.207612 | 0.24638 | missense | Eps15 | Mm_Celera | 4:109379936 | ACCATTGCAAAACCT[A/G]TGTTAGAGGAAACAG | 13858 |
| rs6223511 | snp | C/T | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109310971 | actttgtagaccagg[C/T]tgtcctcgaacccag | 13858 |
| rs6223545 | snp | C/G | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109310993 | cgaacccagaaatcc[C/G]cctgcctctgcctcc | 13858 |
| rs6273645 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Eps15 | GRCm38.p3 | 4:109293155 | ACAACCCTGAGATTC[C/T]ACCTCACACCAGTCA | 13858 |
| rs6311642 | snp | A/G | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109288970 | TTTAGGTTTTATATG[A/G]TTCCTTGGTTGATGC | 13858 |
| rs6313174 | snp | C/T | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109289231 | cccactgatctatct[C/T]tctggtccTTTGAAG | 13858 |
| rs6313719 | snp | C/T | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109289357 | TCTGAATTCATAATT[C/T]TGTTCTATTTATTTC | 13858 |
| rs6322301 | snp | A/T | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109335119 | TAAGTGTAGAGCTCT[A/T]TAACTTAAATGATCC | 13858 |
| rs6327927 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eps15 | Mm_Celera | 4:109367118 | AAATAAAACTGAAAT[A/G]ACAGTGGAAGCTATA | 13858 |
| rs6327940 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Eps15 | Mm_Celera | 4:109367122 | AAAACTGAAATAACA[A/G]TGGAAGCTATAATAG | 13858 |
| rs13470555 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109386701 | AATGGATTTGAAGTA[A/G]ACTATAATTTGTAAT | 13858 |
| rs13470556 | snp | A/C | | | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109386567 | AGCTACCCCACCCCC[A/C]AAAAAATCCTAGTTT | 13858 |
| rs13470557 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109386772 | AGATAAACAAAAATG[C/T]ACCTACAAACTATTT | 13858 |
| rs13474346 | snp | A/G | | | intron-variant | Eps15 | Mm_Celera | 4:109374836 | TCAAAAGCAGCAAAA[A/G]CCAACGCTATCAGGC | 13858 |
| rs28151131 | snp | A/C | 0.124444 | 0.216185 | downstream-variant-500B | Eps15 | Mm_Celera | 4:109387951 | CCTCAAATCCCTTTT[A/C]TGCTGTTTTTGAGAA | 13858 |
| rs28151132 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109387682 | TCATTTTGCATTGAA[A/G]CTTTGTGCTGTTCTT | 13858 |
| rs28151133 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109387585 | TGCTCTCTTCATAGA[C/T]GTTCTCTCATGTTTC | 13858 |
| rs28151134 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109387413 | TATGTAATATGACAT[A/G]AACATATCTATATCT | 13858 |
| rs28151135 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109387344 | AGCTGGGTCATAGAG[G/T]TTCTTATCCTTTGTT | 13858 |
| rs28151136 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109386324 | CCTGTACCCATTTTG[C/T]CTTTGTGGCTGCACT | 13858 |
| rs28151137 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109385785 | CTCTGCCTTCTGGAA[A/C]CTAGCAGATGTAGTT | 13858 |
| rs28151138 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109385682 | AGTACCCTAATTAAA[C/T]GGCTTTGCCTAGACC | 13858 |
| rs28151139 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Eps15 | Mm_Celera | 4:109385519 | GGAACACTGAAGCTA[C/T]TTACCATGTGCATCA | 13858 |
| rs28151140 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109385241 | AAAACAAGTAGTTAG[C/T]ACTCTTTTATAAAAG | 13858 |
| rs28151141 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109384619 | CATTCTGTATCTAAC[A/G]TTCTTCTATGTAGCA | 13858 |
| rs28151142 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109384307 | CCTCCATTTTCACTG[G/T]GAGAGGTTTGATAAG | 13858 |
| rs28151143 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109384020 | GAAGGAGCAAGATAG[C/T]GATCCCTGTTGAATG | 13858 |
| rs28151144 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Eps15 | Mm_Celera | 4:109383873 | GCCCCTGACCGTGGC[A/G]AGTCCCATTTGGGTC | 13858 |
| rs28151145 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109383868 | GCAATGCCCCTGACC[A/G]TGGCGAGTCCCATTT | 13858 |
| rs28151146 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109383652 | GTCCTTTGTCCTATT[A/C]GAAGTGGAGTAACCC | 13858 |
| rs28151147 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Eps15 | Mm_Celera | 4:109383585 | AAATAAACTTAAGAT[C/G]TAAGAATTCTTTCAG | 13858 |
| rs28151148 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109383377 | TGTACAAAGATTTGG[C/T]AGTTTCTAGAGACCA | 13858 |
| rs28151149 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109383272 | TACTATTTGGCAAAT[G/T]TATGATGGTGATTTA | 13858 |
| rs28151150 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109383255 | AGTAAAATCTTGACT[A/G]CTACTATTTGGCAAA | 13858 |
| rs28151151 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109383004 | TTGGGGAAAATCTTT[C/T]CATTTATAGTTTGAA | 13858 |
| rs28151152 | snp | C/T | 0.32 | 0.24 | missense, intron-variant | Eps15 | Mm_Celera | 4:109382823 | GATTCTTCTGATCCC[C/T]TTAAACTGAATGATC | 13858 |
| rs28151153 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109382687 | GTAGGCTTTTGCTCT[A/G]TACACCACCTGCAGT | 13858 |
| rs28151154 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Eps15 | Mm_Celera | 4:109382557 | TTTTGATTCTTGGCC[C/T]GTTTCCTCTTTGTAT | 13858 |
| rs28151155 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109382430 | AATTGCAGTCACTGA[C/T]TCTTACTGCAGCTAG | 13858 |
| rs28151156 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109381928 | AGGAAAAGCATATTT[A/G]AAGAAACTTAAACTT | 13858 |
| rs28151157 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109381870 | CTTGTGTAAACATTG[A/T]TGAAAAGAATCCATT | 13858 |
| rs28151158 | snp | G/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109381788 | TGTTATGTGGTAGCT[G/T]TAACTCAGGGTTTGC | 13858 |
| rs28151159 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109381766 | GTCTGAGCCTCAGTG[A/C]CTTAGTTGTTATGTG | 13858 |
| rs28151160 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109381393 | GGAAAGGATGGTTTG[C/T]TGAAAAGATCATTGA | 13858 |
| rs28151161 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Eps15 | Mm_Celera | 4:109381180 | GGTATGAGATGGCTT[A/G]ATAGGGGACATGTAC | 13858 |
| rs28151162 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Eps15 | Mm_Celera | 4:109380701 | GTTTAGCACTACCCT[A/G]AGGAAAGGTTTGTTT | 13858 |
| rs28151163 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Eps15 | Mm_Celera | 4:109379625 | TTTGTATTCCCTAAC[A/G]CTTTCTTAGTAAGCC | 13858 |
| rs28151164 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109379553 | GCACTGACAAGCATA[A/G]AGTTAGACATTCTTT | 13858 |
| rs28151165 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109379008 | CTATTGAAAAATGCC[A/G]GCCTGGCTAGGTGGG | 13858 |
| rs28151166 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109378750 | AACTCTGGCACTGAG[C/T]GTCCACTACCTATTG | 13858 |
| rs28151167 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Eps15 | Mm_Celera | 4:109378566 | CCAGAAGGTCTGTTC[A/C]GTGTGATAATCAGAG | 13858 |
| rs28151168 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Eps15 | Mm_Celera | 4:109378369 | GATTAATAGGAAGGA[A/G]CAATGCACCATGTTC | 13858 |
| rs28151169 | snp | G/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109378078 | CAGAACTCTATACCT[G/T]ACCTTCCAGTAGCAC | 13858 |
| rs28151170 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109377999 | AAAGTCATATGCTGT[A/G]CTTCCCTTGAAACAA | 13858 |
| rs28151171 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109377897 | GTGATGGCCCTGTAA[A/G]CCACTTGATATCCCT | 13858 |
| rs28151172 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109377889 | ATATGTGAGTGATGG[C/T]CCTGTAAACCACTTG | 13858 |
| rs28151173 | snp | A/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109377836 | AGTGACGTCTGGGTT[A/T]GTCTAAAGTTTGTGA | 13858 |
| rs28151174 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Eps15 | GRCm38.p3 | 4:109377669 | CTGTCCCTCAATATA[C/G/T]GCAAATTTAGATCTG | 13858 |
| rs28151175 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Eps15 | Mm_Celera | 4:109377407 | AATAATAAGTGTCTT[G/T]AAAAAAAAAAGAATT | 13858 |
| rs28151176 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Eps15 | Mm_Celera | 4:109377127 | GACCAACCTGGAAAG[A/G]GCTGTCTTTACCCAT | 13858 |
| rs28151177 | snp | A/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109376937 | TGCACTATCAAAAGA[A/G]TGGATCAGGAGTAAC | 13858 |
| rs28151178 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109376870 | GGGCATGGTGCAGCA[C/T]AGTCAGTTCCTGCAG | 13858 |
| rs28151179 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109376047 | TTTATTTGTTCCTTT[C/T]TTCCTTATTGGTCAA | 13858 |
| rs28151180 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Eps15 | Mm_Celera | 4:109375839 | TTTCTTTAATGTTTT[A/T]AAATTATGTATGTGT | 13858 |
| rs28151181 | snp | A/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109375671 | AAAGCTCAATAAGGT[A/G]CAAATGTGTCTTTGC | 13858 |
| rs28151182 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Eps15 | Mm_Celera | 4:109375663 | TGCTGATTAAAGCTC[A/G]ATAAGGTGCAAATGT | 13858 |
| rs28151183 | snp | G/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109375516 | GAAGCCAGCTCAGGA[G/T]ACTTGTAAGCATTTT | 13858 |
| rs28151184 | snp | A/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109375476 | TGGATAGACACTTCA[A/G]ACTCTGAAAGAAAGC | 13858 |
| rs28151185 | snp | A/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109375426 | ATACAAGTACACGAG[A/G]TGCTGAGTTCTCCTC | 13858 |
| rs28151186 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109375282 | ATTTAGAATTGTGGG[C/T]TTTCAAAATCAGTTT | 13858 |
| rs28151187 | snp | A/G | 0.5 | 0 | intron-variant | Eps15 | Mm_Celera | 4:109375059 | AGAAACAAGCAGAAA[A/G]TAAATCAGACCTGAG | 13858 |
| rs28151188 | snp | A/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109374967 | ATCGTAACCATTTTT[A/G]GCTCAACAATTGTTT | 13858 |
| rs28151189 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109374794 | AAACCTCTCTTTTTC[A/G]TCTCTTTTTCTGGTT | 13858 |
| rs28151190 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109374651 | CACCAGGATGTCAAA[G/T]AGTGTTTCTGCAAAG | 13858 |
| rs28151191 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Eps15 | Mm_Celera | 4:109374523 | GTTAGCTTGTTAAAA[A/G]CCTGGGTGAATGCTT | 13858 |
| rs28151192 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eps15 | Mm_Celera | 4:109374421 | ATGGCGAGCTTGTTC[C/T]TCTCCGGCTCTGAAA | 13858 |
| rs28151193 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Eps15 | Mm_Celera | 4:109374395 | CATTAGCCAGAAGGA[C/T]CCCAGTCAACATGGC | 13858 |
| rs28151194 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Eps15 | Mm_Celera | 4:109374375 | AATGGATGCATTAAG[A/G]GTTCCATTAGCCAGA | 13858 |
| rs28151195 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109374354 | CTCATTATAAAGGCT[C/G]TTAAGAATGGATGCA | 13858 |
| rs28151196 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Eps15 | Mm_Celera | 4:109374239 | TTGTCCATGCTGACT[C/T]TCCGAAGACTTGCAG | 13858 |
| rs28151197 | snp | C/T | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109374221 | AACAGCTCCATCAGT[C/T]TGTTGTCCATGCTGA | 13858 |
| rs28151198 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109374208 | TTTACTGGCAGGGAA[C/G]AGCTCCATCAGTTTG | 13858 |
| rs28151199 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Eps15 | Mm_Celera | 4:109374182 | TACTTAGTGAAATGC[C/T]CATCACTCTGTTTAC | 13858 |
| rs28151200 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Eps15 | Mm_Celera | 4:109374136 | GTTGCGGACATACTC[C/G]GAAAGCTCCTTCAAG | 13858 |
| rs28151201 | snp | C/G | 0.32 | 0.24 | intron-variant | Eps15 | Mm_Celera | 4:109373987 | ACTCTCCATCCCAAT[C/G]ACCACTGGTTCTGGA | 13858 |
| rs28151202 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109373927 | TGTTCTGCTACAAGC[G/T]CCTCTTTTTTGTTCC | 13858 |
| rs28151203 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109373876 | GCAGTGAAGGCAGCA[A/C]GGAGAGGGCTGCATT | 13858 |
| rs28151204 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Eps15 | Mm_Celera | 4:109373816 | ATGTTGTCATAGCAA[C/T]ACTCCTGGGTCTCCA | 13858 |
| rs28151205 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Eps15 | Mm_Celera | 4:109373778 | AAAGCACCACTATTC[C/T]CTGGAAGGCTTTCAT | 13858 |
| rs28151206 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109373747 | GGCTCTTCACTCAGG[A/G]CCTCAGCTTTATAAA | 13858 |
| rs28151207 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109373718 | CATGTGTGTCTTTAT[A/G]CCACTTCAGAATGGG | 13858 |
| rs28151208 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109373540 | GTGTCAGTAAAACCA[A/G]CTAAAAGCTTTGCTG | 13858 |
| rs28151209 | snp | C/T | 0.487535 | 0.077957 | synonymous-codon | Eps15 | Mm_Celera | 4:109373246 | TTGGAAGCACAATGA[C/T]CCATTTGCTCCTGGT | 13858 |
| rs28151210 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Eps15 | Mm_Celera | 4:109372999 | GGATGTTCACATAAA[C/G]TTAACTTGTTAAATT | 13858 |
| rs28151211 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Eps15 | Mm_Celera | 4:109372968 | GACACATGAAGCCTA[C/T]TGAATGTTGGTGACT | 13858 |
| rs28151212 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Eps15 | Mm_Celera | 4:109372768 | CATCTCATAGTTTCT[C/T]TGTTAAAATAGAAGG | 13858 |