SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3683339 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Asb8 | Mm_Celera | 15:98160648 | CTAAGACAGCGGGCT[A/G]CGAGAACTTTCACTC | 78541 |
rs3710011 | snp | A/C/G | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98156219 | TGCCGCCATGCTGCA[A/C/G]TCATGGTTCTGGAAT | 78541 |
rs4139232 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98160885 | GTCATTTCTCTCATC[A/G]CCCCTGCCCTGCCCC | 78541 |
rs6197620 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155253 | GGAGGCGGCTGCCAC[A/G]GAGATGTGAGAGAAT | 78541 |
rs6198763 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155498 | CGCCGAGGGCAATGC[A/G]CTAGACATTGATGAA | 78541 |
rs6199186 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155552 | TTCTTATCCTTGAGA[C/T]ACCAGCCTACTGGAG | 78541 |
rs6199219 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155572 | GCCTACTGGAGGCTG[C/T]CATGCCATTGATGTG | 78541 |
rs31575365 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Asb8 | Mm_Celera | 15:98157935 | CTCCAGGTTCTAGAC[A/G]AAAATGTGGGTCGAT | 78541 |
rs31593347 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98155603 | TTATTTAATGAAATG[A/G]ATAGCTGGGGACGGT | 78541 |
rs31594917 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb8 | GRCm38.p3 | 15:98163854 | AGGACCATCACAGTG[C/T]TCCCTTGGTCGCAGG | 78541 |
rs31602711 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98141985 | CATAAAAATGAGTCT[A/G]TCAGACTGAGGCCAG | 78541 |
rs31630378 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98161734 | CAAATCTGTCTCTTG[C/T]CTTTCAGGGCCCCCT | 78541 |
rs31638144 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Asb8 | Mm_Celera | 15:98160136 | AACATACAAGGCTAA[A/G]CACACAAAATTAGTA | 78541 |
rs31639446 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98137991 | TCCTTTGTATGACCC[C/T]TTCAGCCATAGGCCG | 78541 |
rs31681859 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Asb8 | GRCm38.p3 | 15:98140067 | TTTTCACTCTGGGCA[C/T]TGCTATTAATCATGG | 78541 |
rs31695859 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98162345 | GGCTAATTGCTTGCT[C/T]TGCCTCTGGTTAAAG | 78541 |
rs31708245 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98159264 | AAGATAATAACTTTT[A/T]AAAAGAGAAACAAGC | 78541 |
rs31756158 | snp | A/C | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98157631 | TAGCCATCACTCGTC[A/C]TGCAAGTGGGAGCCC | 78541 |
rs31770138 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98162239 | ATGATGCCTCACAGA[C/G]CTTACTGAAACGTAA | 78541 |
rs31780643 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb8 | Mm_Celera | 15:98150218 | GTACTAGAGTCATCT[A/G]AAACTCAACTGAGAA | 78541 |
rs31783615 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98161913 | GCAGAGTGAGTTTCA[A/G]GACAGCCAGTCCTAT | 78541 |
rs31818694 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98159395 | GGACAACCAGGGCTA[A/T]ATAGTGAGACTTAGT | 78541 |
rs31829649 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98159314 | CTGTAATCCCAGCAC[C/T]TGAGAGACAGAAGCA | 78541 |
rs31867232 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb8 | GRCm38.p3 | 15:98151806 | CCCCTCAGAGCTCAG[A/G]AAACTGCAGAAAAGA | 78541 |
rs31872275 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98140677 | GACTCAGCCCTCCCC[A/G]TGCTGGGATTACAGG | 78541 |
rs31893433 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Asb8 | GRCm38.p3 | 15:98136655 | TCTGCTTATGAGCAT[C/T]GCTGCCCTGGGCAGG | 78541 |
rs31930828 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Asb8 | Mm_Celera | 15:98161792 | TTCCAACCCTACATC[A/G]CCTTTGTCAACTTTA | 78541 |
rs31940997 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98138111 | GCCTTCAAGACCAGT[A/G]CTACCTGGGTGACTC | 78541 |
rs31944674 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98160302 | AGTTATAAAAAACAG[C/T]GTTTATAAACAGGTG | 78541 |
rs31946913 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98166090 | CATTTGCACACGAGT[A/G]CATGTGTGTTATGGT | 78541 |
rs31981127 | snp | A/C | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98160036 | CACATGGTACACATA[A/C]ATGAAGGAACAACAT | 78541 |
rs31993099 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Asb8 | Mm_Celera | 15:98160675 | ACTCTCTTGGTTGAT[C/T]GGCAGTGCGTTTACC | 78541 |
rs31998875 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98138005 | CCTTCAGCCATAGGC[C/T]GTAAAGTACAACAGA | 78541 |
rs32003895 | snp | A/G | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98155951 | CTAAAGGCATATGCC[A/G]CCATATTTTGCTGGG | 78541 |
rs32016048 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98164396 | GGCACTATTAGGAGG[C/T]ATGGCCTTGTTGGAG | 78541 |
rs32019592 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98162318 | TTTGCCCTACCGCAC[C/T]AGAAGTGTCATGGCT | 78541 |
rs32085319 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98162530 | TTTGCCTCTGCTTCT[C/T]GGAGACCTGGACAAA | 78541 |
rs32088726 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98153274 | CTCAGGAAAAGTCAT[A/G]AATTATTTGTTTGTT | 78541 |
rs32100324 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98161834 | ACAATATAGGTGTGA[C/T]GGAACACAGCACTTG | 78541 |
rs32110457 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb8 | Mm_Celera | 15:98151906 | GATCGGTGCAACTAA[A/G]AACTCAGTGACTGTG | 78541 |
rs32130065 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98152351 | CCCATTACAGATGGT[G/T]GTGAGCCACCATGTG | 78541 |
rs32135260 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98159273 | ACTTTTAAAAAGAGA[A/G]ACAAGCTGGGTGTGG | 78541 |
rs32195710 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98148183 | ATATCATTCATGCTT[G/T]TAAGCGGGAGAGAGC | 78541 |
rs32206423 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | GRCm38.p3 | 15:98139365 | AGACAAGGGCAAAAG[C/T]GGCCACAGTCTTCAC | 78541 |
rs32218497 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98157791 | CTAGTGCTATCTTTG[C/T]GCACAGGGACCTTTG | 78541 |
rs32250570 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb8 | Mm_Celera | 15:98160200 | GACTCAGACATAGGA[C/T]GCTTTACAAATAATG | 78541 |
rs32264261 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb8 | GRCm38.p3 | 15:98159576 | AAAAAGGCAAAAAAA[A/G]GGGGGGCCTGGCATG | 78541 |
rs32278431 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98148031 | GGAGAGCTATTAGAG[C/G]TTCAAAGGGGAGACT | 78541 |
rs32279565 | snp | G/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98161461 | GAGCTGTGTGGCAAG[G/T]AGGGGTGAGGGCAAG | 78541 |
rs32292091 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155605 | ATTTAATGAAATGGA[C/T]AGCTGGGGACGGTCT | 78541 |
rs32304683 | snp | A/C | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98160296 | TGGAATAGTTATAAA[A/C]AACAGCGTTTATAAA | 78541 |
rs32312942 | snp | G/T | 0.5 | 0 | downstream-variant-500B | Asb8 | GRCm38.p3 | 15:98134450 | GAAGTGGAGACTTTC[G/T]GTGCACTGTGCCCTG | 78541 |
rs32315487 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98166297 | ATTAGTTTTTAGAAA[A/G]CAATACTGCATGGTG | 78541 |
rs32335512 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98147845 | GATTTGTCGGGACTT[C/T]TACTGAGCGTTTACT | 78541 |
rs32340098 | snp | C/G | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98152290 | TGTGTGTGTGTGTGT[C/G]TCTGCATCTGCATGT | 78541 |
rs32375546 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98144672 | AACAGCTGTCTGAAA[A/G]GTATGCGAGGCTGTG | 78541 |
rs32377715 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98135666 | GGGAGGCGATGCATA[A/C]GTCACTGTTATGTGT | 78541 |
rs32385635 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98138113 | CTTCAAGACCAGTAC[C/T]ACCTGGGTGACTCTT | 78541 |
rs32397642 | snp | A/T | 0.5 | 0 | intron-variant | Asb8 | GRCm38.p3 | 15:98136886 | CAGTGCTGGGATAGC[A/T]GCTGCCTCACTCAAA | 78541 |
rs32402504 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98161986 | CAAATCCTGCCTGAT[G/T]GCTGGAATCTTTGCA | 78541 |
rs32402829 | snp | C/G | 0.375 | 0.216506 | intron-variant | Asb8 | GRCm38.p3 | 15:98144859 | ACCTGATGTGGTTGT[C/G]TAAGTTCCTGGTACA | 78541 |
rs32403439 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb8 | Mm_Celera | 15:98151920 | AGAACTCAGTGACTG[C/T]GGCAGCATGAACTGA | 78541 |
rs32475449 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98139702 | CTTATAATTTCAGAG[A/G]TTTAGTCCATTATCA | 78541 |
rs32488965 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Asb8 | GRCm38.p3 | 15:98147796 | ATAGGCTGCCCACCC[A/C/T]GGTTGTCTTGAGGTG | 78541 |
rs32490655 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98162340 | GTCATGGCTAATTGC[C/T]TGCTTTGCCTCTGGT | 78541 |
rs32500128 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Asb8, Ccdc184 | GRCm38.p3 | 15:98167561 | AGCCCCCCCCCCCCC[C/G]CCAGGCAGACGGTCT | 78541 |
rs32504671 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98158651 | TTCCCAACCTTTCAA[C/T]CCTCTAACACTAGAT | 78541 |
rs32510882 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb8 | Mm_Celera | 15:98151549 | CTATGCCCTATACCA[C/T]CCCATGGCCAAGAGC | 78541 |
rs33859245 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98151991 | TGGGAGGAAAGTAGA[C/T]ACCAGCCCCCATCCC | 78541 |
rs36269697 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Asb8 | Mm_Celera | 15:98134274 | TTGGTGGGTAGAGTT[A/G]GGCTTTAGCATTTTA | 78541 |
rs36278551 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Asb8 | Mm_Celera | 15:98155642 | CACCCCGGAGCTCAG[C/T]GAAGACTTTTCAGGA | 78541 |
rs36306639 | snp | A/G/T | 0.497778 | 0.0332592 | intron-variant | Asb8 | GRCm38.p3 | 15:98165241 | GAGTCTGGCATCCCA[A/G/T]TGACCCAAGCTTATA | 78541 |
rs36338896 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Asb8 | Mm_Celera | 15:98154091 | GTCCTTTCAACATGT[A/C]CTTATTAAATGCTAT | 78541 |
rs36419468 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Asb8 | Mm_Celera | 15:98161281 | ATTTAAAAACGACCA[C/T]GATTCCCTTCCTGCG | 78541 |
rs36420675 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb8 | Mm_Celera | 15:98136565 | ACAATGTGGGAAGTG[A/G]TGAGCAAGATGGGAT | 78541 |
rs36486787 | snp | C/T | 0.497778 | 0.0332592 | upstream-variant-2KB | Asb8 | Mm_Celera | 15:98165735 | CTGACGTAAGCCTAT[C/T]TTGGCAGCAAACGTG | 78541 |
rs36491451 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Asb8 | Mm_Celera | 15:98147113 | TACTGTACTACAAAA[C/T]GGAGCTTGAGAGCAC | 78541 |
rs36491892 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Asb8 | Mm_Celera | 15:98165029 | TACTCAGAATCGCAG[C/T]TTTCATAAGAATGTG | 78541 |
rs36559137 | snp | C/G | 0.473373 | 0.11227 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98166567 | GCAGTTACTGAACTA[C/G]AGGTGACCAATGACA | 78541 |
rs36562905 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98167006 | CTGAAAGGAAATTGT[A/G]TTCAGGTCTTCTGAA | 78541 |
rs36576025 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B | Asb8 | Mm_Celera | 15:98134187 | TATGATTCCCAAGCA[C/G]GATGAAGAGCAGAAT | 78541 |
rs36631196 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Asb8 | Mm_Celera | 15:98152919 | CGGTAGGTATACGTC[A/G]GATGTAAGGTAATCG | 78541 |
rs36637049 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98135317 | ATATGGAAGTGCTCC[C/T]GAATGCCAAATTCTG | 78541 |
rs36648910 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Asb8 | GRCm38.p3 | 15:98153602 | GATGCCCATTTTCTG[A/G]TATGGTTGACTGGCT | 78541 |
rs36692963 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98166398 | TTTATGTAAACATTC[C/T]GACCCTGGGCACTTT | 78541 |
rs36710355 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98134762 | TCATTTGGGTGTAGT[C/G]TCCAGCCAGCTTTTT | 78541 |
rs36716428 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Asb8 | Mm_Celera | 15:98134572 | AAAGGCTGAAAGAGC[C/T]GAGCAATTTCTTATA | 78541 |
rs36726595 | snp | C/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98155365 | GTGCTCATGCATAAA[C/T]GAAGGAGCCACTTAC | 78541 |
rs36732906 | snp | A/T | 0.375 | 0.216506 | intron-variant | Asb8 | Mm_Celera | 15:98136883 | TTGCAGTGCTGGGAT[A/T]GCTGCTGCCTCACTC | 78541 |
rs36750147 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Asb8 | Mm_Celera | 15:98141179 | TTTAGTAACGTAAAT[C/G]CTAATGTCACCATGA | 78541 |
rs36772845 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98135517 | TCCTAGGAAATGGGT[G/T]ACACTGGTGACTGAA | 78541 |
rs36783499 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Asb8 | Mm_Celera | 15:98163343 | CAAAGATGTCCTTAG[A/G]ATCTGACAATTGAGA | 78541 |
rs36828041 | snp | G/T | 0.375 | 0.216506 | utr-variant-5-prime, intron-variant | Asb8 | GRCm38.p3 | 15:98145612 | TCACCGAACCGCGGG[G/T]CAGATCGGTCCGGGA | 78541 |
rs36921420 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98135597 | AAGCAACTAAGCAAT[A/G]ACACGGCAAACAAGT | 78541 |
rs36944130 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb8 | Mm_Celera | 15:98136925 | TCAAAGTCCTAGTTT[A/G]CAGAGGGCCTAAGAT | 78541 |
rs36973278 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Asb8, Ccdc184 | Mm_Celera | 15:98166958 | GGTCCGTCAAGAAAA[C/T]GATGTCAGCTGAGGT | 78541 |
rs37145724 | snp | G/T | 0.5 | 0 | intron-variant | Asb8 | Mm_Celera | 15:98161192 | CACAATACGGTGAAC[G/T]TGTGTAATAGCACAC | 78541 |
rs37184736 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98135207 | AGGATGGCCTGGCAG[C/T]TCTGGGACTGCTGGG | 78541 |
rs37310680 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Asb8 | Mm_Celera | 15:98134786 | GCTTTTTAAAAAGTG[C/T]TTTCCAACTTGCATA | 78541 |
rs37551953 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb8 | Mm_Celera | 15:98162788 | GGGACATAAAGGCCT[C/T]CGTTTTATCACAGGC | 78541 |