SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6171753 | snp | C/T | 0.5 | 0 | intron-variant | Asb12 | Mm_Celera | X:95516607 | cagagagttaggaat[C/T]gatacacctcaagac | 70392 |
rs13483889 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Asb12 | Mm_Celera | X:95553506 | GGTTGGAGGTTGAGT[A/T]GAAGAAGAAATATCT | 70392 |
rs29084674 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95521944 | TAAGATACAAATACG[A/G]TCAAGGACAATGAAG | 70392 |
rs29084675 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95521293 | TAAAATGGCAGAATA[C/T]TAAGGTGTGGCTTCT | 70392 |
rs29084676 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95521264 | TTTTAAGACAAAAGT[G/T]GGAGGAGTAATAGTA | 70392 |
rs29084677 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95520210 | AAAAAATGGCCTTCA[G/T]GGATCCTGCTTCTAT | 70392 |
rs29084678 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95519778 | CATGCCTACTAGTAA[A/G]TCTATGCTTCCAGGA | 70392 |
rs29084679 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95514120 | TCATAGAATATTTGG[A/C]TACATGCACACCAAA | 70392 |
rs29084680 | snp | C/T | 0.5 | 0 | intron-variant | Asb12 | GRCm38.p3 | X:95510443 | TGGACTGCATCGCTT[C/T]TTCACATGCCAATTC | 70392 |
rs29084681 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb12 | GRCm38.p3 | X:95510384 | CTTTTCACTCACTCA[C/T]ACAACTTTAGAACAC | 70392 |
rs29084682 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95509749 | GCTGAGTTAGCCAAT[A/G]ATGCTTTAGCTATAA | 70392 |
rs29084683 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95495679 | AAAACCCAAAGAACT[A/G]CCACTATCTTTATCT | 70392 |
rs29085194 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95495580 | TCTAACATTCCTCCA[A/G]TCCTAATCTCAAATT | 70392 |
rs29085195 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95495553 | ACCCCTAACACTGTC[C/T]TGAAAACATTATCTA | 70392 |
rs29085196 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Asb12 | Mm_Celera | X:95495031 | TCTTAGCTAGTGTTG[A/G]GATTGAAGGTCCTGA | 70392 |
rs29085197 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95494799 | TCTTTCCTCTTCCCA[C/T]GATGGCTTACTTCTT | 70392 |
rs29085198 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95494792 | AGTCTGTTCTTTCCT[C/T]TTCCCATGATGGCTT | 70392 |
rs29085199 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95494751 | TCTCAGGTCATGTCT[A/G]CTTTTGCCATTTTGA | 70392 |
rs29085200 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95493023 | GTAGAATTCAGTCCT[A/G]TGGTGAGAATTTTTG | 70392 |
rs29085201 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95492971 | CACTCTGAATTATCT[C/G]TCTGCAGTTTACACA | 70392 |
rs29085202 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95492128 | CTAGTCTCAATTTTT[A/G]TATGTTACAGATGCT | 70392 |
rs29085203 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95492068 | AGAGAAAGGACCCAA[C/T]TATTTTTTTAAAGTA | 70392 |
rs29085754 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95491238 | CTGGTACAGGACAAA[A/C]AAAATCGGTCTTGCT | 70392 |
rs29085755 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95490945 | TATCTTCTTAAATGC[C/T]ATTAGGCCTTTCTAC | 70392 |
rs29085756 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95490644 | AAATTTCTGGCCACC[C/T]ACATGGTTTTAAACA | 70392 |
rs29085757 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95490007 | GTCAGTGGAACCTTA[A/T]GAGCATGGGCTATAG | 70392 |
rs29085758 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95489841 | GAAAGCCACATATAT[A/G]CAGAGAGAGAAGAGT | 70392 |
rs29085759 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95489701 | AAGATGAAGTAGACC[G/T]GGCCACCCTCAGCCA | 70392 |
rs29085760 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Asb12 | GRCm38.p3 | X:95489614 | TCCTCTGTTAAAAAG[C/G/T]TGTACCTTTAAGTGA | 70392 |
rs29085761 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95489190 | AAGAAAACCAGTATC[A/G]AGCACATGGAATGCA | 70392 |
rs29085762 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95488999 | AGCTCATGTCAGGCC[A/C]AGGGCTTGTTATTAG | 70392 |
rs29085763 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95488638 | CAGAGGATCGCTGCA[A/G]CCCTTTTTATATTAG | 70392 |
rs29086314 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95488567 | CTCACTGATGGAACT[A/T]CATGGCATAAAACAA | 70392 |
rs29086315 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb12 | Mm_Celera | X:95487622 | TTGGTGACAAGAGAC[C/T]TGTGGATAGAAACTA | 70392 |
rs29086316 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Asb12 | Mm_Celera | X:95483824 | AACTATGTGGGACCA[C/T]GACTACTCACAGCCT | 70392 |
rs29086317 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb12 | Mm_Celera | X:95483727 | CTTCCCATCTCTCAT[C/T]TTTCTGGACCCTTCC | 70392 |
rs29086318 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb12 | Mm_Celera | X:95483470 | GCCAGGCCATCCTTC[C/T]GTACTCTCAGCCACA | 70392 |
rs29086319 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Asb12 | Mm_Celera | X:95480906 | TGGATCCTAAAGAAA[C/T]AGGAATTGCCCTAAG | 70392 |
rs29086320 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95476909 | AAGAAAATCCAGCTA[A/G]TCTATTGTGTAGCTT | 70392 |
rs29086321 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95476783 | TTGGGGACTCGGAGC[A/G]AAAATGCTGAAGTTC | 70392 |
rs29086322 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95476647 | CTCGCCTTTGCTTCA[C/T]GTTTAGCTACACTAC | 70392 |
rs29086323 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95475833 | TGAAACCAAACACTG[C/T]GGGTGATGAGTATGT | 70392 |
rs29086924 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95475789 | AATATGGTCAAAGGA[C/T]ACAACACATTCAGAT | 70392 |
rs29086925 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95473977 | CTCTTCATTTCGGTC[C/T]CATAGCTTTAGCCCT | 70392 |
rs29086926 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95473323 | ATCATTCACATACCA[A/G]ACTCCTATATACTTC | 70392 |
rs29086927 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95472814 | GCTCAGATCTCCCTA[C/T]TTTCCCAGATATTTT | 70392 |
rs29086928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95472735 | CCCTCTAAGTCTTTT[C/T]GCTAAGTAAAGTTTG | 70392 |
rs29086929 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95472207 | ATCAAACTGTCATCC[A/G]TGAGCTTTCTAATAA | 70392 |
rs29086930 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95471892 | TTTATAGCTTGGAGA[A/C]TTAGCATAAACTGTT | 70392 |
rs29086931 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95471765 | CTTATCAATGCCAGA[C/T]TCTATGTTTACTCTT | 70392 |
rs29086932 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95471760 | GCATCCTTATCAATG[C/T]CAGACTCTATGTTTA | 70392 |
rs29086933 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Asb12 | Mm_Celera | X:95471365 | AGTGAAAAGTGGTGT[C/T]TGTGCTTTGACATCC | 70392 |
rs29087524 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95470667 | CTAAGACCAGAGAAT[A/G]TATAAATGCTTTCTA | 70392 |
rs29087525 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95470504 | ATGAGCATCAATTCT[A/C]AGTGTAATTCCAAGT | 70392 |
rs29087526 | snp | C/T | 0.231111 | 0.249285 | missense | Asb12 | Mm_Celera | X:95470409 | TGTGACTGGTTCGCC[C/T]GGCAGAGGGATCTGC | 70392 |
rs29087527 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Asb12 | Mm_Celera | X:95470241 | ATAATACGCCAGAAA[C/T]GTTATGAGGTGTATT | 70392 |
rs29087528 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Asb12 | Mm_Celera | X:95470047 | AGGTACCACAATAGG[C/T]CTGTTTTCTCTCTTC | 70392 |
rs29087964 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558405 | TGATGCAGCAATTAT[A/C]ACCAACTGTCCACCC | 70392 |
rs29087965 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Asb12 | Mm_Celera | X:95555717 | GAACTCAAACTAAGA[C/G]TTCCATTCTATATGC | 70392 |
rs29087966 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95555623 | AATGCCCCAACTGGT[C/T]CCTTTGGCTGCCCAG | 70392 |
rs29087967 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb12 | Mm_Celera | X:95555411 | AAAAGAAAAAAAAAA[C/T]CTGCTTACCATCTTT | 70392 |
rs29087968 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95555256 | ATGAAACCTTGGGCT[A/C]GTCAATACTGAATAA | 70392 |
rs29087969 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95554534 | CAGATGCTGGTGCTG[C/T]ACATGGGTGTCAATG | 70392 |
rs29087970 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95554500 | GGCTGAAAGGGGCTG[G/T]AGTTTCAGAAAGCAA | 70392 |
rs29087971 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95554389 | AGTAGGAAAGCACGA[A/G]ACACTCACCGAGTAT | 70392 |
rs29087972 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95553842 | CTTAAACACTCAGTA[C/T]GTCTCAAGAGCTATT | 70392 |
rs29087973 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Asb12 | Mm_Celera | X:95553115 | ACATATTCATCACAA[A/G]AAAATTATATTGGTA | 70392 |
rs29088384 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95552558 | GCACTCCTCAATAGG[A/G]ATGTTTCCATAAACA | 70392 |
rs29088385 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95552527 | AGAGGTTAGCTGTTA[C/T]GACTAAGCTAGCTTT | 70392 |
rs29088386 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb12 | Mm_Celera | X:95552461 | TTTCTGTTTTGACTT[C/T]CTTCTTTGACTTACT | 70392 |
rs29088387 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95552364 | TCTTTCCATAAAGCT[C/T]TCATTTTACACTCCT | 70392 |
rs29088388 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95552287 | GTAGGACAGATTGAA[A/G]TTCTATAATGAAAAG | 70392 |
rs29088389 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95552169 | ACCTAAAGGGAGACT[A/G]GAAATGCTCAAGGAG | 70392 |
rs29088390 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95547834 | TCTTAGAAACTGTGA[A/G]GACACCAGAGTCTAG | 70392 |
rs29088391 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95547788 | CAGTTCTTTAAAACA[A/G]TCCTATAGCTCCAAT | 70392 |
rs29088392 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb12 | Mm_Celera | X:95547462 | CTCAACCTACAAAAG[C/T]CCAACAGGCTTAACT | 70392 |
rs29088393 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb12 | Mm_Celera | X:95544581 | GCAGACCCAGAAATG[A/G]CACCTCTGTCAGGCA | 70392 |
rs29088714 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95544373 | GGACTCAGGAACACT[A/G]GACTCCTTTTTAAAT | 70392 |
rs29088715 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95544105 | GGAGGCACAAAGACT[G/T]CCCTTAACCTCTTTT | 70392 |
rs29088716 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Asb12 | Mm_Celera | X:95542476 | TATACCATTGAAACT[A/G]TATAAACTACATATT | 70392 |
rs29088717 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Asb12 | Mm_Celera | X:95542365 | TCTGTCAGGGGCCCA[G/T]GAGATCAAAGAGAAG | 70392 |
rs29088718 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95537935 | AACATGTGGGAGGGT[A/G]AACTGCACAAGGTAT | 70392 |
rs29088719 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Asb12 | Mm_Celera | X:95534980 | GATATCCCACTGAAA[A/T]AACAAAGATAGATTG | 70392 |
rs29088720 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95528832 | TAACACAAAAACCTC[A/G]AACCAAAAATTAATC | 70392 |
rs29088721 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95528432 | TATACTTCGAGAAAA[C/T]GACTTGCCAGGCCAA | 70392 |
rs29088722 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95523673 | GATTCTGGTTGTACT[A/C]CCTGAGGCTCCTCTT | 70392 |
rs29088723 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Asb12 | Mm_Celera | X:95523633 | ATTTAACCATTAAAA[A/T]TTTCACAGTTCTGCA | 70392 |
rs29934149 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95540148 | GTTGAGAATTCTTTG[A/T]TTAGCTTTGTACCCC | 70392 |
rs31156639 | snp | A/G | 0.5 | 0 | intron-variant | Asb12 | Mm_Celera | X:95480267 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 70392 |
rs31185335 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb12 | Mm_Celera | X:95539719 | CGGTGTGTGTGTGTG[G/T]GGGGGGGGGACAGAA | 70392 |
rs31189647 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95545322 | ATATATATATATATA[G/T]ATATATAGATAGATA | 70392 |
rs31403592 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95474576 | CCAGGACTGTTACAT[A/G]GAGAAACTGTAAGAG | 70392 |
rs31856093 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb12 | Mm_Celera | X:95523404 | GGAAAGGCTGATTGT[C/T]ACTTAGAAGGAAACA | 70392 |
rs31856894 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95520322 | TCTCTAACTTGTCAA[A/G]CCTGAATAAGCAGGC | 70392 |
rs31856895 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95518540 | ACCTATTACCTTTTA[A/C]AAATTGGGTCAACTG | 70392 |
rs31856896 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb12 | Mm_Celera | X:95513750 | ACTCAGTAACTAAAC[A/G]ACTGCATGAAGTGTA | 70392 |
rs31856897 | snp | A/T | 0.375 | 0.216506 | intron-variant | Asb12 | Mm_Celera | X:95512986 | GGGTAAGGTCTTACC[A/T]TGTGCGGCAGGTGGT | 70392 |
rs31856898 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb12 | GRCm38.p3 | X:95510239 | CATATTTATTACCCT[C/T]TCTTCTTTCCTGTAA | 70392 |
rs31856899 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95509056 | AAGAAAGACTAACCA[C/T]AGCTCTATATTTAAC | 70392 |
rs31856900 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Asb12 | Mm_Celera | X:95495157 | TTCTGGCTGACTAAT[A/G]CCTAGGTGGAGAAGG | 70392 |
rs31856901 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95494730 | ATGTATTTGGAGATG[C/T]CAGCCTCTCAGGTCA | 70392 |
rs31856902 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95494694 | TCTCCTCTACAAAAT[C/T]TGATTCTTAAGCCTT | 70392 |
rs31856903 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95492917 | CTAGAAAACAACTAA[C/T]CCCATCATGCCCTGG | 70392 |
rs31857484 | snp | A/C | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95490680 | CAGGAAAGTATAACC[A/C]AAATTAAAATGATCC | 70392 |
rs31857485 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95490588 | TAAGGTAAATTCTAA[C/T]TAGTGTCCATTCTAC | 70392 |
rs31857486 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Asb12 | Mm_Celera | X:95490461 | GTAGTTAAAAGTTTT[A/T]AAAGTACCAAACTGG | 70392 |
rs31857487 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb12 | Mm_Celera | X:95476847 | TCTATATTATAATGA[A/G]CCTCCAAATAGAAAT | 70392 |
rs31857488 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb12 | Mm_Celera | X:95476472 | CATAAATAATACCCT[C/T]GTTTTGAAAATGATA | 70392 |
rs31857489 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95474307 | GTCTCCACTGTCTTG[C/T]CTCAACTGTTATAGT | 70392 |
rs31857490 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95473371 | GGCTGCATCCACCTT[C/T]AATCATAAAAAGCAC | 70392 |
rs31857491 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Asb12 | Mm_Celera | X:95471161 | TGAAGCTATATTTGA[A/C]GCCCAGACTGGTAGT | 70392 |
rs31857492 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Asb12 | Mm_Celera | X:95470311 | AGGTATCATGCATTA[A/G]GTTCCTGAGAAAGTT | 70392 |
rs33853414 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb12 | Mm_Celera | X:95488750 | TTTCCATGGTACATT[C/T]ATAGGCTTCTTCCAA | 70392 |
rs33872040 | snp | A/C | 0.5 | 0 | intron-variant | Asb12 | Mm_Celera | X:95475465 | CATTGTGGAATCAAC[A/C]TAGGCATCCAACAAT | 70392 |
rs33874296 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb12 | Mm_Celera | X:95545326 | ATATATATATATATA[G/T]ATAGATAGATAGATA | 70392 |
rs46240464 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95506103 | GAGGAAGAGAAGGGT[C/G]ATCCTGTAGAAAGAC | 70392 |
rs46558914 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95540031 | CCAACAGATTGGGAA[A/T]GGATTTTTACCAATC | 70392 |
rs47506605 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95506206 | TTGATATGAGATCCC[C/T]AACACACATACAGTA | 70392 |
rs47551501 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501608 | ATGAAACCAAGAAGT[A/G]GTTCTTTGAGAGAAT | 70392 |
rs48211402 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95506193 | CAGCATACACCAGTT[G/T]ATATGAGATCCCCAA | 70392 |
rs49976879 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95549158 | ATTATAATTTCATGC[A/C]TGTGTACAATGTATT | 70392 |
rs50325935 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500947 | TCTCCCAGTATTATT[A/G]TGTGAGTTGCAATGT | 70392 |
rs50520957 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95506204 | AGTTGATATGAGATC[A/C]CCAACACACATACAG | 70392 |
rs52454775 | snp | C/G/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95537758 | GGGGGAAGGGAATAG[C/G/T]GGGAGGGTGTTTTTT | 70392 |
rs107932284 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95506101 | AAGCTGAGGAGAAGG[A/G]TGATCCTGAAGGAGA | 70392 |
rs108355645 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95509959 | AACTGTAATGTTACT[A/T]GTACCATAATTTTGG | 70392 |
rs108550248 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95506203 | TGTACGTGTGTTGGG[G/T]GCCTCATATCAGCTG | 70392 |
rs211718336 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95483675 | CAGGTAGATCCAGCC[A/G]GACCAGGCCCCTTTC | 70392 |
rs211735935 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95543338 | CCCGAGGATCTGAGT[A/G]TGAACTCGGGACCCC | 70392 |
rs211757368 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95482145 | CACCCTGTCATTCTA[-/T]TTTTTTTGACATAGA | 70392 |
rs211778119 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472552 | ACCAAGAATTCCTTT[C/T]GATTACTAATACCTC | 70392 |
rs211800980 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95483093 | CACCACCAAAAGAGT[A/T]CACATGGTGGGACTC | 70392 |
rs211807362 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95495471 | ATCCTAGCTCAACCT[C/G]CAACTATAACCTTAA | 70392 |
rs211808226 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95552990 | TAAATTCAAGGGCAG[C/G]TCTTTTCTTACACAT | 70392 |
rs211812728 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95533002 | CAATGTGAAGAGTCA[C/G]AGTTTTAGAATGGTT | 70392 |
rs211846279 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95553777 | ATGGACTTTTTAAAA[A/G]CGTGATGACCAAATT | 70392 |
rs211960869 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95543198 | GACTTTAGTGAAGAG[-/C]AGTCTATACATGCTC | 70392 |
rs211971643 | in-del | -/G | | | intron-variant | Asb12 | Mm_Celera | X:95522359 | TAGGGAAAGAAACAA[-/G]GAAAAAATTTTATTT | 70392 |
rs211977777 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95503583 | TCCTGTCACTCTGCA[A/C]AAAACTCAAGTCCAT | 70392 |
rs212007375 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95502824 | TGATATGATAGTATA[G/T]ATTAGTGATCCTGAA | 70392 |
rs212045576 | in-del | -/CTT | | | intron-variant | Asb12 | Mm_Celera | X:95528675 | AGTCCAGGAGAGTCC[-/CTT]TTTCAATAAATTAAG | 70392 |
rs212060158 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95494758 | TCATGTCTACTTTTG[C/T]CATTTTGAGGTGGAA | 70392 |
rs212065859 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95512648 | TCACTACTATTCATT[C/T]ATATGATCTATTTCC | 70392 |
rs212103541 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95531935 | AGGCCCAACAAGGAG[A/C]TGATGAGACAGAAGC | 70392 |
rs212148841 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95522263 | AACAAAACAACAACA[A/G]CTATAACGACAACAG | 70392 |
rs212189632 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95511712 | TCCCAGCAAGCATCA[A/T]TTGCAAATTTCTTGG | 70392 |
rs212191666 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95522938 | AACAAAATCTCTAAC[A/G]TGCCAGAAGTAGGTC | 70392 |
rs212208841 | snp | C/T | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95469987 | TTAGATTTTTCAAAA[C/T]CTTTAAACCAGGGCA | 70392 |
rs212269595 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95493285 | GACTCCTACCAGTGA[G/T]GGGTATGGAGCTTGA | 70392 |
rs212273820 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95539717 | GCCGGTGTGTGTGTG[G/T]GTGGGGGGGGGACAG | 70392 |
rs212329129 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95551773 | CAAACATGGCATATT[A/G]AGTTGCAATCAGATT | 70392 |
rs212341379 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95480408 | TAACAATGCATATGC[A/G]TACATCCATATGTTA | 70392 |
rs212399877 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95481712 | GGCTGGAGCATCCCG[A/G]ACCCTTACTATATTT | 70392 |
rs212415818 | in-del | -/TT | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558179 | ACCAGACTGAGCTGC[-/TT]TTTTTTTTTTTTTTG | 70392 |
rs212426816 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95492464 | ATGTGCCCTTCTCTA[C/T]GTGCAATCTTGCTTC | 70392 |
rs212428145 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95541342 | GTAGGGGAATGCTAC[A/G]GCAGGAAGCAGGAGT | 70392 |
rs212476585 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531232 | TTAATCCCAGCACTT[A/G]GGAGGCAGAGGCAGG | 70392 |
rs212488357 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95500115 | GATGGAGAAGTGTAG[A/G]CTCATATTTTTCAAA | 70392 |
rs212491125 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95550847 | AAACCTGTTGCTCTT[A/G]AAAAGGACCTGAGTT | 70392 |
rs212504479 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95509954 | TTCATAACTGTAATG[C/T]TACTAGTACCATAAT | 70392 |
rs212596528 | in-del | -/TGTTCG | | | intron-variant | Asb12 | GRCm38.p3 | X:95526689 | GTCTGTCTGTCCGTC[-/TGTTCG]TCTCTCTCTCTCTCT | 70392 |
rs212666719 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95521145 | GAAGAAAAAATACTC[C/T]AGTAAAAAGATCCCT | 70392 |
rs212743300 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95529276 | TCACAGAATGAGAAG[G/T]CTCCAGAAGATCACA | 70392 |
rs212777857 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95536316 | TGGGAGTGGGTGGGT[G/T]GGAGTATGAGCAGGA | 70392 |
rs212779084 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95520314 | TCCCACGATCTCTAA[C/T]TTGTCAAGCCTGAAT | 70392 |
rs212799359 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95477825 | AGAATATTACAAACA[C/T]ACTTTGGGACAGATA | 70392 |
rs212835193 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95549727 | TATGAAAGACATTAA[C/T]TCCAAAGCATTTATG | 70392 |
rs212856859 | snp | A/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500821 | AAGGACACTTGATGC[A/T]TAACAAAGAAAAAAA | 70392 |
rs212858234 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95528650 | GGCCAGGTTCAGCTA[A/C]AGTGAGTTCAAGTCC | 70392 |
rs212887388 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95549228 | AATACTCCTGCTGGC[C/G]CACTTCTCCCAAACT | 70392 |
rs212928306 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95489710 | TAGACCGGGCCACCC[C/T]CAGCCAATTGGATAC | 70392 |
rs212989956 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95476966 | GTTAGTATATGCGTT[C/T]TATAAACAAAGAGCT | 70392 |
rs213015544 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95488800 | AATAAACACATCAGA[A/C]AAACAAAATTCCAAA | 70392 |
rs213027297 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95557232 | GTCAAGTCATATTAA[G/T]GAAGACAGAATCTAA | 70392 |
rs213071115 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507358 | AATTTTTTCTGCCTA[C/T]GAGATATGCATGGAT | 70392 |
rs213112829 | snp | C/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558413 | CAATTATCACCAACT[C/G]TCCACCCTGGTTATT | 70392 |
rs213115608 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95498402 | TTTTTGGCTAATATC[C/G]CCTTATTAGTAAGTA | 70392 |
rs213188267 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95554640 | AAGTTAACTCTTTAA[-/C]TTACCTCAGGCATCA | 70392 |
rs213253185 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95537108 | TAAGTGGATATTAGC[C/T]CAGAAGCTTGGAAGA | 70392 |
rs213281393 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95517235 | TAGCTTTAGTTGTTG[C/G]CTGAGGTCCTGTGAA | 70392 |
rs213304697 | snp | A/C | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501916 | GGTCTCATACCAAAA[A/C]CCTGTACTCAACAAA | 70392 |
rs213332837 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95492826 | GTAAAGGATATAAAA[G/T]AAAGGAAATCTTCTA | 70392 |
rs213415945 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500902 | AGACACCCACATTTG[C/T]AAAGGAAACTTTACT | 70392 |
rs213417316 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95511509 | AAGCTTAATTTGAAA[A/T]TTTCCTTTAAAACAC | 70392 |
rs213428019 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95499060 | CTGGTGTGGTGAGGA[C/T]ATCCTCTTGGAGACA | 70392 |
rs213565205 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95510062 | ATGCAATCCACCAGA[A/G]AAGAGTATTGAGAAG | 70392 |
rs213645354 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95507962 | GAAAATGGAAGAAGG[A/G]GGTGTGAGGATGGGA | 70392 |
rs213661561 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95522034 | AATTATAGAAAAGCC[C/T]AGTAAGATCAGAAAA | 70392 |
rs213702360 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95477959 | TAATGTCCTAGACAG[A/G]GCTGAAAGTTAGGTT | 70392 |
rs213708908 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95537270 | AGACTGAAAGAATGA[A/C]CATGCAGAGACTGCC | 70392 |
rs213745875 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95520378 | AATAAAGTTCTATGG[C/T]TTCTAACCATTCTGC | 70392 |
rs213752216 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95538040 | CAGGAGCTTATCATC[C/T]GTATAAGTGTGGATT | 70392 |
rs213787912 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95549321 | GTGTATTCATGACTA[C/T]AAAAACCATGACATA | 70392 |
rs213788603 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95477110 | AGTAAGATATATACA[A/T]TTAAAGAAGCAACTA | 70392 |
rs213802565 | in-del | -/AAG | | | intron-variant | Asb12 | Mm_Celera | X:95520180 | GGCATTTAAAAAAAA[-/AAG]AAGAACCAAAGAGAA | 70392 |
rs213817906 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95549965 | TTGAAACTAATTTTT[A/T]AAACTTTTATAATAA | 70392 |
rs213869954 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95493463 | CCAACTTGAGACCCA[C/T]CCCATGGTCAAGCAC | 70392 |
rs213893946 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529436 | GATAGTTAGAACAGA[A/G]AAAAAAATGTTTAAT | 70392 |
rs213909285 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479852 | AAAAGAAAAGAGAGA[C/T]GAGACATTAAAGTAA | 70392 |
rs213973526 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95508047 | TTTATGAGAAAAAGA[A/C]AAAACACTTAAAATG | 70392 |
rs213994590 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95521346 | ATTCAATGGCAATGG[A/G]AGGACAAATCCCTTT | 70392 |
rs214038072 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95517447 | AACCTGAACACCAAC[A/C]TAGCCATAAAACCTT | 70392 |
rs214119781 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558721 | CTCAAAGCTTTTGAG[A/G]TAGCAGGCTACATGA | 70392 |
rs214124726 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95507427 | AGTTGCCCAAATTGA[A/T]CCCTACCCCATGGGA | 70392 |
rs214125026 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95518140 | GCATCTTCTCCTAAA[G/T]ATCTGTTCTGTTTTG | 70392 |
rs214128522 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95499107 | GATATGGAACAGTCC[A/G]AGGGCAGACTAGGAG | 70392 |
rs214128649 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95505391 | AGTTAACTCAGAACC[-/A]AAAAGGACATGCATG | 70392 |
rs214144443 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95490078 | AATTACACATAGAGC[A/G]TAAATTAATTTACTA | 70392 |
rs214191496 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95530092 | TCCTAAGCCTATTAA[C/T]CTGCTTGCATTTTCT | 70392 |
rs214253177 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95475435 | TGTTGGTAATAGTGC[A/T]ATTAACAGTAGCCAC | 70392 |
rs214270456 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95547434 | TAGTGTAACTGGAAT[G/T]TAAGGAATAGATCTC | 70392 |
rs214317433 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95476123 | GCTTCATGGGGCTTT[A/T]AGGATAAATAATTAT | 70392 |
rs214344684 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95555552 | TTGACATGGTTGTGT[A/G]ATATTCTTATTCAAC | 70392 |
rs214363031 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95491080 | TCTGGACAATTTCAT[A/G]AACAGGAACCAACAG | 70392 |
rs214378192 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95556635 | TGAACACTTCCTTTG[C/T]AATGGACTCCAAATC | 70392 |
rs214378258 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95545644 | ATGCATTTCTCTTTC[A/G]GGAATATTCTTATAT | 70392 |
rs214432909 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95506464 | GTCATCAGGGAAATG[A/C]AAATCAAATCCACTC | 70392 |
rs214521104 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95527685 | ATAAATGGGTATGCC[A/G]CAGTATAAAATGATT | 70392 |
rs214525388 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95499817 | CTACTACCACCACCA[A/C]CAACAACATCAATAT | 70392 |
rs214527283 | in-del | -/CCAAATATAAACC | | | intron-variant | Asb12 | Mm_Celera | X:95495506 | AATACCAGCCCTGTT[-/CCAAATATAAACC]CCAAACTTACTATTA | 70392 |
rs214589903 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505279 | TGATACAGCAAATGT[A/G]GTTCACTTACAAAAT | 70392 |
rs214590145 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95516118 | TAAATAACAAGAATT[A/G]AATAATCATTATTCA | 70392 |
rs214655258 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95535443 | ATTATATATGCATCA[G/T]TACAGGGGAATGAAC | 70392 |
rs214693593 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95487557 | TTCCTTAGGTACCCC[A/C]CCCCTTCTAACATTC | 70392 |
rs214697172 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95514771 | CAACAGTCAAACAGA[C/G]CCATAAAACAGTCAA | 70392 |
rs214701505 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95528322 | GTGGCTTTAGAAAAA[C/T]AACTACATTTCATAC | 70392 |
rs214715364 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95473150 | ATGCTTCCCGGGGCA[A/G]CTAAGATAAAGATAA | 70392 |
rs214746236 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95544329 | ACTCTCTATTTAAAT[A/C]CGAAGCTTCTCTGCT | 70392 |
rs214848892 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95497567 | ATATCCTAACACTGC[C/T]GAACCACAAGGAAAT | 70392 |
rs214935606 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95538702 | AAGGAAACTCAAAGG[-/AA]AAAAAAAAACACATG | 70392 |
rs214966434 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95488510 | ACCACCTTGGCTAAT[A/T]ACAAAATGTAATGCA | 70392 |
rs214979709 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95534699 | TGGGAGATCTTTCCA[A/T]CTGAATCACAAAAGA | 70392 |
rs214983232 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529205 | TGGCAGTTTTAGTGG[A/G]ACAGTTTTACAGAGA | 70392 |
rs215056339 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536265 | ATCCTGTGAAGGCTC[A/G]ATGCCCCAGTGTAAG | 70392 |
rs215070366 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95525207 | AAACACTTGGTCCGC[C/T]GTTGCTGGCACTCTT | 70392 |
rs215089235 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528569 | TGCTTACATAAATAG[A/G]AAACCATAATCTCTG | 70392 |
rs215159056 | snp | A/C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95535585 | CAATAAAAAAAAATT[A/C/T]GTAGGCAAATGGATG | 70392 |
rs215199083 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95533676 | CCTCAAACACAGCCA[C/G]ACATTCTAATCCCGT | 70392 |
rs215225802 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95497054 | ATTAAACAAGCCTGT[A/C]GGAGGTGAGCAGCAT | 70392 |
rs215242962 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498332 | TTGAGGCATCCTACC[C/T]GGACCCTTCAGCTTG | 70392 |
rs215245729 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95508196 | ACCCTAAAACCGGCT[A/C]TAATAGATACAGGGA | 70392 |
rs215279876 | in-del | -/AAG | | | intron-variant | Asb12 | Mm_Celera | X:95557749 | ATGATGTCATCCCAT[-/AAG]AAGATGTGAACTGGT | 70392 |
rs215299028 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95552072 | TCTCTCTCTCTCTCT[-/C]TCTCTCTCTCTCTCT | 70392 |
rs215323245 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95497862 | GCATAAAAGATAAGA[C/T]TAAAGAAAAAAAAGG | 70392 |
rs215329588 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95507320 | GGAGGAGGACATCTA[A/T]CCACCCACAAAACAT | 70392 |
rs215433609 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95518488 | CTCTACTTCCAAAGT[G/T]TTGGGATTGTAAGTA | 70392 |
rs215484544 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95506548 | TGTGGAGAAAGGGGA[A/G]TATTCCTCCATTGTG | 70392 |
rs215618710 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95545451 | GGTAGAGGCAGGCAG[A/G]TTTCTGTGCATTCAA | 70392 |
rs215620813 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95533744 | ATGGAGGCCATCCTC[A/T]TTTTCACCACCATAA | 70392 |
rs215648364 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95534413 | TGTCTGTCATTGTAC[A/C]AATACCATGCAGTTT | 70392 |
rs215656530 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95524453 | TCCTGTGATTTTATA[A/G]TAAATTATTATGTAT | 70392 |
rs215659345 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95476229 | TGTAGTATATATGTC[A/G]TGTTTTTCTATGATT | 70392 |
rs215714022 | snp | A/C/T | | | intron-variant | Asb12 | Mm_Celera | X:95544438 | CTTGTTGGGATCAGG[A/C/T]TATCCTCTACTTTAC | 70392 |
rs215771262 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505178 | CCCCACCATGCCAGA[A/G]AGGCACATATTTCAC | 70392 |
rs215793599 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95556894 | AGATAGTAGTTTAAC[C/T]AAGAACCTTCAGAAA | 70392 |
rs215815071 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95508945 | GAATTTTAGGATGAA[A/G]CAACCCCTTTCCCTT | 70392 |
rs215857137 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95496820 | AACCCTAGAATTACC[C/T]TATTTTTGGTCTGGA | 70392 |
rs215873207 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95530138 | AAATACTACAGAGAG[-/A]GGGGGGGGGGCAGAA | 70392 |
rs215877909 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95488631 | GAGCCCTCAGAGGAT[C/T]GCTGCAACCCTTTTT | 70392 |
rs215880958 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95503669 | GTGGAAAATATCCAC[A/G]AACACATTGCCACAG | 70392 |
rs215991723 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95516405 | AATGTTTAACATCCT[C/T]AGTCACCAGGAAAAT | 70392 |
rs216090124 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95532701 | ATCATTTTCACTTCA[C/T]ATCCTCCCCCTCAGG | 70392 |
rs216096622 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95489613 | ATCCTCTGTTAAAAA[A/G]TTGTACCTTTAAGTG | 70392 |
rs216102621 | snp | G/T | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558249 | CAGCTATTATCAAAC[G/T]TGCTGTGAAGACCAA | 70392 |
rs216141507 | in-del | -/GT | | | intron-variant | Asb12 | Mm_Celera | X:95539706 | AAAACCATCAAGCCG[-/GT]GTGTGTGTGTGTGGG | 70392 |
rs216147021 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95548984 | GAACTAAATGTGAAA[A/G]CACTCCTTCAAAAAC | 70392 |
rs216173103 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95542220 | AAAATAAAATTCTTA[G/T]ACAAAGGGAAATATC | 70392 |
rs216174696 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95476875 | AATGAAGCCATGCAT[A/G]GCTCAATTAGATATG | 70392 |
rs216191495 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95526173 | TCTCTGTCCCTCCAC[C/T]CCTCTCTTCCTCCAT | 70392 |
rs216211810 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531991 | GTCGGGGACTCCTGT[A/G]GTTGAATTAGGGAAA | 70392 |
rs216221718 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95470810 | GGATGATGATTTGGA[A/T]CCCTGAGACCTACAA | 70392 |
rs216284089 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95523850 | TATTTACTTGCTTCC[-/T]TTTTTGTTTGTTTTC | 70392 |
rs216289554 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95541536 | AAAACACAATTTATG[A/G]TAAATATAAATCCAA | 70392 |
rs216293654 | snp | C/G | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95470092 | AAGATCCATGTGCTT[C/G]TCAGGGCCAGATGTA | 70392 |
rs216363038 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95526408 | ATATTAATGGATTTT[A/G]CTACCAATGCATTTG | 70392 |
rs216370561 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95484627 | GATACAAAGGTGTAA[A/C]TATTGAGCTGCTGGC | 70392 |
rs216370744 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95554538 | TGCTGGTGCTGTACA[G/T]GGGTGTCAATGAGCA | 70392 |
rs216393670 | in-del | -/AAAA | | | intron-variant | Asb12 | Mm_Celera | X:95515627 | ATAGATTGGATTAGG[-/AAAA]AAAAAAAAAAATCCC | 70392 |
rs216398158 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95527422 | AAAGCTGAATCCAAA[A/G]CCTTCCTTTTTCATA | 70392 |
rs216400749 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95516506 | ATAGCATGCTGCTGA[G/T]GATGTGCAACAAGAG | 70392 |
rs216440527 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95473268 | GTAAAACCCTTTTCT[A/C]AATCACTTTTCTTTA | 70392 |
rs216459382 | in-del | -/GG | | | intron-variant | Asb12 | GRCm38.p3 | X:95510118 | GACAAAAGTTCCTTA[-/GG]GGAAAAAAAAATAGT | 70392 |
rs216507107 | in-del | -/AA | | | intron-variant | Asb12 | GRCm38.p3 | X:95510531 | CATCTTCTGTGAAGT[-/AA]AAAAAAAAAATCACA | 70392 |
rs216539450 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95484685 | TGGTAATTGTATTTT[C/T]TTCTCTGTAACAAGA | 70392 |
rs216541531 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95497525 | GGCACTGCCAGAACC[A/G]AGATATTCTAGCACA | 70392 |
rs216556383 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95555288 | TTTTGAAGCTGTGTT[A/C]TCTCTATTCCCTACC | 70392 |
rs216561337 | in-del | -/AGGC | | | intron-variant | Asb12 | Mm_Celera | X:95477649 | GTACTAGGAAGCCTG[-/AGGC]AGGATTTCCAGTTTG | 70392 |
rs216563984 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95517189 | TCTTTTGTAGCCAGG[A/C]GAGGCTTCCAGTGGT | 70392 |
rs216598368 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95486099 | AAGCAAAAGACACTG[A/T]CAATAAGAAAAAAAG | 70392 |
rs216621308 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95496891 | TTTCTAACTAGAAAC[C/T]TAACCCAGAACTAAC | 70392 |
rs216636043 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95534297 | GTTGAAAATGCTGTC[-/T]TTTTTTTTCTGAATG | 70392 |
rs216703377 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95554596 | GAGATCAAAGCTGGA[C/G]ACTGGCAGAAAGCCC | 70392 |
rs216718050 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95524272 | CATTTTTCTACAAAA[A/G]GAAGTGTTTATGTTA | 70392 |
rs216727631 | in-del | -/AAAAA | | | intron-variant | Asb12 | Mm_Celera | X:95505436 | TAAGTGGATATTAGC[-/AAAAA]AAAAAAAAAAAAATA | 70392 |
rs216733158 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95537239 | GAAGGAGTTACAGAG[-/A]AAAAGTGTGGAATAG | 70392 |
rs216819559 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95525279 | GTATGGAAATTGAGA[A/G]TTGAAAGCCTTGCTC | 70392 |
rs216824663 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95475212 | TAAAATTAAAAGGTT[C/G]TTCTCAGTAAAAGAA | 70392 |
rs216836299 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95513669 | AATGAGCCCATCATC[A/C]TTCTAGTTTTTGAAG | 70392 |
rs216858313 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95525186 | CCTATACAGGCTCAG[C/G]CATTTAAACACTTGG | 70392 |
rs216924761 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95532818 | GAAGAGACTAAGAGA[C/G]GGTAAGTATTAGGGG | 70392 |
rs216958409 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95524314 | AAATCAAGTACCCCT[C/G]CCAAGGAGTATCAAT | 70392 |
rs216979910 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95483655 | AGAACCCTGGAAAGG[C/G]CTTCCAGGTAGATCC | 70392 |
rs216987931 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95553886 | GTCAGTTCTTCTTTC[A/G]TGTACTTACCAGCCA | 70392 |
rs216997407 | in-del | -/AATA | | | intron-variant | Asb12 | Mm_Celera | X:95482917 | TGCCAGAGCCTGGCC[-/AATA]AATACAGCTGTGGAT | 70392 |
rs217021300 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95532117 | GCCAGGCAGCATACA[A/C]CATTTGATATGAGGC | 70392 |
rs217072617 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95483807 | CACAACCCAGAGACC[C/T]CAACTATGTGGGACC | 70392 |
rs217082286 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95494673 | CAGTCCCTTCCCAGT[C/T]CCTATTCTCCTCTAC | 70392 |
rs217084693 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531263 | CGGATTTCTGAGTTC[A/G]AGACCAGCCTGGTCT | 70392 |
rs217141527 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95482977 | GGAATCCCAGTAGAA[A/C]AGTTAAGGGAAGGAC | 70392 |
rs217172674 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95493647 | GTTGGAGGAAGAAGT[A/G]AAGGCTCTGAGGAAA | 70392 |
rs217205265 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95494593 | GGGGTTGAAAGGGTA[A/G]AAGGAAAAGAGTGAA | 70392 |
rs217205726 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95512737 | GATGGAGTAGGAGTG[A/G]AAGTTAAAGATCACC | 70392 |
rs217312456 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95522190 | AGCAAATTAAAAATA[C/T]AGATTATTTGAAATT | 70392 |
rs217355331 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95482860 | AAGATATTGTTGATG[C/T]TATGAAGCACTTGCT | 70392 |
rs217369895 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95530248 | TGATTTTTGTAATTG[A/T]ACCAACCTTGCATCC | 70392 |
rs217392378 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95531139 | TAACAAGCCAAAGGG[A/C]CCAAGTGAGGATGCC | 70392 |
rs217393746 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95523199 | GGGCCTTGGTAAAAC[C/T]GATAACTGTAGCATT | 70392 |
rs217497208 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500769 | ACCATATGACACAAC[C/T]GAGTCTCCAAAGAAA | 70392 |
rs217497240 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95491262 | TCTTGCTAACATCTA[A/T]GATAAAGTGTTCTTT | 70392 |
rs217544946 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95492380 | CTTTACATCCTTCAG[A/G]ACCAAACTGACTCAT | 70392 |
rs217557844 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95482095 | TAAAGAGCTGTCTGC[C/T]TCTGCCTCTTGAGTG | 70392 |
rs217561012 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95552203 | CTTAGCACCAGCCCC[C/T]CATCTCAGGAATAGT | 70392 |
rs217564380 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95500024 | TTCAAAGCAAACAAA[C/G]ATAATCAAGAAGCAA | 70392 |
rs217574113 | in-del | -/AAA | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559484 | AGACCTGTAAATATT[-/AAA]AAAAAAAAAAAACTG | 70392 |
rs217624506 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95475369 | AAAATTCCTCATGGG[C/T]ACATATGTTAAGGAC | 70392 |
rs217645983 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95545544 | CAAAAAAACTAAAAT[A/C]AAAATTAATAAATAA | 70392 |
rs217649236 | in-del | -/CTG | | | intron-variant | Asb12 | Mm_Celera | X:95499789 | TTACTACTACTACTA[-/CTG]CTGCTACTACTACTA | 70392 |
rs217692827 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95534586 | GCTCTTTCTAAGTCT[A/C]TGAAGTATAGACTTT | 70392 |
rs217702172 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95535071 | GGACTTGATAAAATT[C/T]GTAGGCAAATACCTG | 70392 |
rs217836222 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95552378 | TTTCATTTTACACTC[A/C]TCATACTCATCTAGA | 70392 |
rs217846141 | snp | C/T | | | missense | Asb12 | Mm_Celera | X:95471600 | CCGGTGCCAGTGTCC[C/T]CCTCCTCCTTTTCAG | 70392 |
rs217857901 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95522517 | ACAAAAATAAACAAA[C/T]AAAACAAAGCAAGCA | 70392 |
rs217887179 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95523665 | TAAACTTTGATTCTG[A/G]TTGTACTCCCTGAGG | 70392 |
rs217938295 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95544549 | TAAGGGAAGAGGAAG[A/G]TGACTGTAGCCCCTG | 70392 |
rs217981480 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95551297 | TGAAATGAACAGACA[C/G]TTCTCAAAAAGGAAA | 70392 |
rs218028167 | snp | A/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95510226 | TTAACTGGTCAAGCA[A/T]ATTTATTACCCTCTC | 70392 |
rs218030206 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95480930 | CCCTAAGAATCTTAT[A/G]TTGGTAGAAGGAAAC | 70392 |
rs218044227 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95482411 | TGTAGAATGTCAAAT[G/T]AGTTACTTATTTTCA | 70392 |
rs218065195 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95514695 | TGTGGATCCCTCAGA[A/G]CATCTCCCACTGGCT | 70392 |
rs218090218 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95520742 | ATGGAAGAGTTCTCC[A/G]AGGCTGGGAGTCCTG | 70392 |
rs218107518 | in-del | -/GGGG | | | intron-variant | Asb12 | Mm_Celera | X:95530137 | TAAATACTACAGAGA[-/GGGG]GGGGGGGGGGGCAGA | 70392 |
rs218122347 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95521529 | ATCTACTATCCCGAC[G/T]TCTCCGGGTCCTACC | 70392 |
rs218123931 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95509752 | GAGTTAGCCAATAAT[A/G]CTTTAGCTATAATAA | 70392 |
rs218146212 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95503711 | CTAAATAACACAAAG[A/G]GCTCAGACTCTCAGA | 70392 |
rs218210355 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505246 | GGAAATTACCCAGAT[A/G]TCCTCCGACAGAAGA | 70392 |
rs218261048 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95478446 | GCCAGAGAAACCCCA[A/G]CTTTAACTCACTTCC | 70392 |
rs218315888 | in-del | -/TACCTG | | | intron-variant | Asb12 | Mm_Celera | X:95513339 | CAGAATGTTAGCATT[-/TACCTG]TTTACTATTTAAGAC | 70392 |
rs218380518 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95477469 | TTTGGTTTTTGTGGG[C/T]GCTAGGACATTCCTT | 70392 |
rs218382336 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95491577 | TATTAGATATTTTCT[C/T]TATTTACATTTCAAA | 70392 |
rs218406482 | in-del | -/GG | | | intron-variant | Asb12 | Mm_Celera | X:95508071 | AAAATGATATATAGT[-/GG]TGGGGTCAGGGGATG | 70392 |
rs218450269 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95550199 | TCTAAACAATGTAGG[A/T]AAGGTTAGTTTGTAG | 70392 |
rs218534107 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95553657 | ATCACTCTAAAATTG[A/G]ATACTCCTATATTAA | 70392 |
rs218538448 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95542309 | TTCTGATTCTGAAAA[G/T]TCCCAAAAAGATCTC | 70392 |
rs218559068 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95549470 | GCTGAGTACTCAATA[C/G]TCATTTACTCTCATC | 70392 |
rs218602632 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95543148 | TTCTTTATAGAACAT[C/T]ACTTTATTGCATTTA | 70392 |
rs218614582 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472375 | GTTCTAGAACAGAGG[C/T]ACCTAACAAATTGAT | 70392 |
rs218669382 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95476292 | GAGCTAAGGTGAATC[-/TT]ATAGATAAATTAGTT | 70392 |
rs218672919 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95552716 | TTAATAATCAGAGAT[A/G]AGGTATAAATTCAGC | 70392 |
rs218699553 | snp | G/T | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559162 | TTGACAGTGCTGGGA[G/T]TAAAGATTGTTTGAA | 70392 |
rs218750126 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95518668 | TGTTTCAACAGAGGA[C/T]AGAGCACTAAGGTTC | 70392 |
rs218823841 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95527916 | CCACTGATGCAACTT[A/C]TTCAGGGTGTATCTA | 70392 |
rs218843406 | snp | A/C | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502569 | TTGTAGTGATCAAAG[A/C]TTCAAGGCACTTATC | 70392 |
rs218852603 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95517598 | CCTGGATAGACAGAA[A/G]CTGAAGACTGGCAAA | 70392 |
rs218882996 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95511637 | TGGGCATGAGGCCTG[C/G]CATGGAGTATGGTTG | 70392 |
rs218915038 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95476326 | TTCACCTTAGAGATA[A/G]GAAATTTGAAGATTA | 70392 |
rs218919022 | snp | A/C | | | intron-variant | Asb12 | GRCm38.p3 | X:95526942 | AGCCATCTTTATAGC[A/C]CCTACTTGATAAGTA | 70392 |
rs218929815 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95555772 | AGCTCTCACCAAACA[C/G]GGGTTCCCCTTCACA | 70392 |
rs218994218 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501993 | TTAGCAAAGTTAAAT[C/T]GAGATCTGATGTAAT | 70392 |
rs219035459 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554946 | GCAAAGTATGATGCA[C/T]ACACAAGGCCCTGGT | 70392 |
rs219067345 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95512430 | TTTTTGGTTTTTGAT[G/T]GGAAGAGACAGATTA | 70392 |
rs219104122 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95484880 | CCTTCCCTGCCGGAG[A/G]AGAGGTGTCTGCCCC | 70392 |
rs219113840 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95487672 | AAGCTGGTCTCCACA[C/G]TAATGCTACTTCACA | 70392 |
rs219158430 | in-del | -/AATAAT | | | intron-variant | Asb12 | Mm_Celera | X:95547484 | GGCTTAACTTGTTGA[-/AATAAT]AATTTTATGTTTTAT | 70392 |
rs219256496 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479942 | GGTGAAGTAGATTGA[A/G]ATACATTATGAAAAT | 70392 |
rs219265743 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95550908 | TACAACCATCTGTTA[C/T]TCCAGTTCCAGGGTA | 70392 |
rs219268870 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95537581 | ACCATCAACCAAAGA[A/G]TACATATTGTGGGAC | 70392 |
rs219271867 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95541222 | CAATCAAAAAAAAAA[A/C]GTGGAGGGACTTGTG | 70392 |
rs219278270 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95550805 | ATAAGTTACTTTTAC[A/G]CTAGAGAGATGTCTC | 70392 |
rs219319277 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95538818 | GCTCATATCTAAACA[C/T]AGTAAAAGCAATATA | 70392 |
rs219357990 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95521443 | AGCAGATGCTCTAGA[G/T]AGGAAGGAACGTCAA | 70392 |
rs219363024 | snp | C/T | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95469714 | TACCAATATTAGTCT[C/T]GATTTCAAAGGCTTT | 70392 |
rs219404665 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95550328 | TCCAACTCTCAGAAC[A/T]GTACAGGAAAGAGAA | 70392 |
rs219414968 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95509351 | AATGGTTTAACAATA[C/T]AAGATCCTTAATTAG | 70392 |
rs219429414 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479591 | CAGGGATGGGGGCAC[-/AG]AGAGAGAGAGAGAGA | 70392 |
rs219454234 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95499393 | CTGCAAGGGGAAAAG[G/T]ACAAGTAACATAAAA | 70392 |
rs219466439 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95500227 | AAAGAAGAATATGGA[C/T]CTGTTTAGAAATACT | 70392 |
rs219493285 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95535796 | CATCTTAGAAGGGGG[A/G]AACAAACACACATGG | 70392 |
rs219499629 | in-del | -/CTC | | | intron-variant | Asb12 | Mm_Celera | X:95551964 | TTCCTCCTTCTCCTT[-/CTC]CTCTTCCTCTTCCTT | 70392 |
rs219519578 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95536633 | AATATCAGACACAGT[C/T]ATGGCTGGAAAAAAA | 70392 |
rs219559089 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95508643 | CTATAATCTGTATAA[C/T]GGCCTATAATCTGTA | 70392 |
rs219583378 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95548235 | AAAGAAAGAGAAAAG[C/T]ATAAAGAAACTAAGG | 70392 |
rs219593325 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95550110 | AAGGATAAATAAGTA[C/G]TCTTCCAAGTGAACT | 70392 |
rs219677984 | snp | G/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95478254 | CCAGTGTGTGTGTGT[G/T]TGGGGGGGGGGGGGG | 70392 |
rs219725225 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95546206 | CTTTGGTTACTTTCT[C/T]TAGCTCCTTCTTTAG | 70392 |
rs219737107 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95506661 | CCAAGTGTCCCATTC[C/T]TGGGCATATACCAAA | 70392 |
rs219781838 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95541635 | GGTCTAGCTAATATC[A/G]TTGCATGATGTTATT | 70392 |
rs219787723 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95555400 | TTCAAATGCCAAAAG[-/AA]AAAAAAAAAACCTGC | 70392 |
rs219819377 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95531536 | AAAGAATTTGTAACA[G/T]GCTACCTCTGGAGGT | 70392 |
rs219844357 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95476425 | GAACACATCTATAAC[C/T]TTGTACTTTTCAAAT | 70392 |
rs219883280 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95516589 | ATCAATGTGGCAGTT[C/T]CTCAGAGAGTTAGGA | 70392 |
rs219884709 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505701 | CCTCAGGAGGTAAGA[A/G]GCTAGGGAAACCCTC | 70392 |
rs219902090 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95532201 | TTCACTTAACCTTCA[A/T]GAGACTGGAGGTCCC | 70392 |
rs219972891 | in-del | -/AAA | | | intron-variant | Asb12 | Mm_Celera | X:95492524 | AGAGTTCAAAGACTC[-/AAA]AAAAAAAAAATCTAC | 70392 |
rs219974224 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95515680 | AATTAACATTCAAAA[C/T]AAAGAGCATGTTAAA | 70392 |
rs220030499 | in-del | -/AAAC | | | intron-variant | Asb12 | Mm_Celera | X:95497741 | GGAGCAATAAAGAAA[-/AAAC]AAACCCAGGGAAATC | 70392 |
rs220081970 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95483888 | ACTCATGGCCTTTGC[A/T]TTGTTCTACCAGTTC | 70392 |
rs220093603 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95472983 | ATCTGAATATGTATT[C/G]TTAGGGTCCAACATA | 70392 |
rs220115998 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95492991 | CAGTTTACACAAAAG[G/T]GGCAGGTTCTGAACC | 70392 |
rs220118274 | in-del | -/TTT | | | intron-variant | Asb12 | Mm_Celera | X:95483596 | GTCGAATCAAGTCTA[-/TTT]TTTTTTTGTTTTCCT | 70392 |
rs220210634 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95493842 | CCCTGACTCTATTGC[C/T]TGCCTGTTCCCATAA | 70392 |
rs220228305 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95544711 | ATGAGTATATTAAAA[C/T]CATAAAAGAAACCAG | 70392 |
rs220249950 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501185 | AAAATCAAAATGACT[C/T]CTTGTATCTTATCAA | 70392 |
rs220285691 | in-del | -/ATAGATAG | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559176 | GTAAAGATTGTTTGA[-/ATAGATAG]ATAGATAGATAGATA | 70392 |
rs220328008 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95543640 | ACAGTGGAGTCCTTC[A/G]TGCCATATATCAGTT | 70392 |
rs220328071 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554761 | CTCATCTTCTGATAC[C/T]AACAAAGGCTCTTAT | 70392 |
rs220410242 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502118 | TAAGCCCAGGACCAG[A/G]TGGTTTTAGCACAGA | 70392 |
rs220412904 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95529752 | AGACACACACACACA[A/C]ACACACACACACAAA | 70392 |
rs220452851 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498624 | AAGGAGGTCCAATAA[C/T]AGACTCAAATTGGGC | 70392 |
rs220465056 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95499245 | AAAAACTTCCACAGT[A/C]TAAAGAAAGAGATGC | 70392 |
rs220465067 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95489321 | AGGATTAGGAGATGG[A/G]GCCTTGCCAGAGTAG | 70392 |
rs220486619 | in-del | -/GCAGAATGTAG | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559687 | AGAAAGCTGTCTTGA[-/GCAGAATGTAG]GCCATCGCTTGTAAC | 70392 |
rs220490832 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95554086 | TATACATAGATTGGG[A/G]GAAGCGTGGCTACAG | 70392 |
rs220541508 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95514260 | AGGAGGAAGGAAAAA[C/T]GATTTTAAAAATACC | 70392 |
rs220578480 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95503925 | TTTAAAAATAGGACA[C/G]AGAGGTAAACAGAAA | 70392 |
rs220605252 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95530378 | TAAGCAAAATTGGTC[C/T]GAAGTTCTCTTTTTT | 70392 |
rs220610401 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95537560 | CCCAGGGTTCCCAGG[A/G]ACTAAACCATCAACC | 70392 |
rs220646135 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95513002 | TGTGCGGCAGGTGGT[A/G]TGTTTCAGACAAAAG | 70392 |
rs220677380 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95491234 | ACTCTGGTACAGGAC[-/AA]AAAAAAAATCGGTCT | 70392 |
rs220704138 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95555992 | ACATATGTAAAGGTC[-/A]AAAATTAATCTCAGA | 70392 |
rs220831329 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95499287 | CAAGAAGCTTACAGA[A/C]CACCAAATACATTGG | 70392 |
rs220870476 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95552646 | ATGACAATAATCATT[-/A]AAAAAAATACTACAG | 70392 |
rs220872402 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95536911 | CTCATGATATCCTAC[C/T]GAAGTAACAACGATA | 70392 |
rs220902981 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95527755 | ACTGGATCTTCTGGT[A/G]AGGAACTTTGCTTTC | 70392 |
rs220927889 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95543783 | TCTCCCCCCCCCCCC[A/C]CCCTTGGTGCCATTT | 70392 |
rs220963105 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95508373 | GCACAATCCACTTGA[C/T]GGACTCTAGGATCAC | 70392 |
rs220972374 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95534735 | CATGGTGTACACTCA[C/G]TGATAAGTGGATATT | 70392 |
rs221006674 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95526882 | TTGGATGCTGGGAAT[C/T]TACCCCAAGTCCTCT | 70392 |
rs221016017 | in-del | -/AAGGTGAC | | | intron-variant | Asb12 | Mm_Celera | X:95514047 | AGAATACTACATAGA[-/AAGGTGAC]AGACAAATAGTAAGT | 70392 |
rs221072110 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95534126 | CCCAAGTGTTTGAGG[C/T]TCTTCCCCACTTTCT | 70392 |
rs221171122 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95535728 | AAGATAAATTTACAA[A/T]CCACATGAAACGCAA | 70392 |
rs221209265 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505515 | AAAGTGCCCAAGTGA[A/G]GATGCCTCAGTCCCA | 70392 |
rs221221757 | in-del | -/TTCTTTTCTTTTCTTTTCTTTTCTT | | | intron-variant | Asb12 | GRCm38.p3 | X:95551808 | ATGGAACAATTCTTC[-/TTCTTTTCTTTTCTTTTCTTTTCTT]TTCTTTTCTTTTCTT | 70392 |
rs221236209 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95543403 | GTAGCCCTCTCCCTA[A/T]CTGTGCACATTGTAG | 70392 |
rs221238063 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95532300 | TGAGGAACTGTTGAA[A/G]AGCATACCAGGAGGT | 70392 |
rs221255775 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95496398 | TATGTGAGTGTTTTG[C/T]CTGCCTAAAGAGGAT | 70392 |
rs221269468 | snp | A/C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95497165 | TTCCAGACCCAGGAA[A/C/T]ACCCAGGCTAGACCC | 70392 |
rs221273237 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95533031 | TTATTCTAACTATAC[A/T]GGCATTCACTGAGAT | 70392 |
rs221280712 | in-del | -/CA | | | intron-variant | Asb12 | Mm_Celera | X:95499751 | GTGTGTGCACTCATG[-/CA]CACACACACACACAC | 70392 |
rs221309085 | in-del | -/AT | | | intron-variant | Asb12 | Mm_Celera | X:95551254 | ATTAAGCAACAAAAC[-/AT]ATTTTTCTAGTCAAT | 70392 |
rs221318317 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507677 | CTGGGGCTTGGGGGG[C/T]TCACAGAGACTGATC | 70392 |
rs221335952 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95498747 | AGCCCAATAAGAGCT[A/G]ACTGAGACAGATGCA | 70392 |
rs221341968 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95542571 | CTTCTTAACCTCTAT[A/G]CAGGCTTGCAGGCTG | 70392 |
rs221346185 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95548028 | AAGATGAAGTGCGTC[C/T]TGTTGTTAGTATATT | 70392 |
rs221401071 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95504555 | CTAATAAAAGAGAGA[A/G]TGGCAAACAGCCTTG | 70392 |
rs221409100 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95497911 | TGACATAAAATATCA[A/G]ATAAATCTGGGACAT | 70392 |
rs221439109 | in-del | -/AAATAAATAAATAAATAAAT | | | intron-variant | Asb12 | Mm_Celera | X:95519131 | GTGGGCTATTTCCAA[-/AAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 70392 |
rs221449483 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95541847 | AGCCAGTCATTTTCC[C/T]CATGAGTGGTGATAA | 70392 |
rs221454227 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502264 | GATACAATAACGTAC[A/G]AGAATTTCAGACCAA | 70392 |
rs221513334 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95503031 | TAGTGTAACTCTAAC[C/T]AAGTAAGTGAAAGAC | 70392 |
rs221566413 | snp | A/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501388 | TTATGGGACCTAATG[A/T]AAGCAATGCTAAGAG | 70392 |
rs221566453 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95511889 | GTCATCCACGGCCTT[A/G]TCTGACTCTTAGAAT | 70392 |
rs221582650 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95506648 | TCTACATCAAGACCC[A/T]AGTGTCCCATTCCTG | 70392 |
rs221617782 | in-del | -/TTC | | | intron-variant | Asb12 | GRCm38.p3 | X:95551865 | CTTTTCTCTTCTCTT[-/TTC]TTCTTCTTCTTCTTT | 70392 |
rs221637385 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95510400 | ACAACTTTAGAACAC[A/G]CCAAGGGATAGGACA | 70392 |
rs221674852 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95470539 | ATCTATTCTGCCATG[A/G]CTATTATAGTAATGC | 70392 |
rs221687443 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95478612 | TCATCCTGGAATGAG[C/T]TCTCGATCATCTTTT | 70392 |
rs221746593 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95546089 | TCCTCCCATTGATAG[A/C]TGACTAGGCCATTCT | 70392 |
rs221748901 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95515637 | ATTAGGAAAAAAAAA[A/T]ATCCCCTCGACATGT | 70392 |
rs221799902 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95524762 | CCCCCAGGATGGGCC[A/G]TGACTTGGCACGAAA | 70392 |
rs221799966 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95491706 | CTGGGACATCAAGCC[C/T]TCATAGAACCAAGGG | 70392 |
rs221823668 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95525765 | GGGGAGATCTCTAAA[G/T]TTAGGGTAAATAGAC | 70392 |
rs221895361 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95534927 | AGGTCATCCAACAAC[C/T]TGTTGTTGTCCAAAA | 70392 |
rs221916041 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95483825 | ACTATGTGGGACCAT[A/G]ACTACTCACAGCCTT | 70392 |
rs222004321 | snp | A/G | | | utr-variant-5-prime | Asb12 | Mm_Celera | X:95495015 | CGTTGTTTTCACTGG[A/G]TCTTAGCTAGTGTTG | 70392 |
rs222014765 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95495712 | AACTTACCATATCCT[C/T]GCCCTAGAATTAACC | 70392 |
rs222015618 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95483327 | ATAAAATAACCAATT[A/T]AAAAAAAAAACCTTG | 70392 |
rs222035112 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95511117 | AGTCTCTTTAGAGTA[-/T]TTTTTTATTAAAGAT | 70392 |
rs222150633 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95497245 | GAGGTGAGCTGTGCT[C/G]TGTTCTCACAGCTCC | 70392 |
rs222174570 | in-del | -/G | | | intron-variant | Asb12 | Mm_Celera | X:95534513 | TTTTTTTTTTTTATT[-/G]TTGAGAATAGTTTTT | 70392 |
rs222191625 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528779 | AGTCAAGAACAGTAT[A/G]TACGTGGACAAGGTA | 70392 |
rs222193122 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95539842 | TCTAAGTGGATCAAG[G/T]AACTCCTCATAAAAT | 70392 |
rs222227639 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95518787 | CCTGTAGTATCATGG[A/G]GTGAATAGAGATTTA | 70392 |
rs222244817 | in-del | -/AAGGCC | | | intron-variant | Asb12 | GRCm38.p3 | X:95525007 | GTTTAAAAAAAAAAA[-/AAGGCC]AAAAAGACCAAAAAG | 70392 |
rs222297571 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95480492 | AAGAAGATAGCAGAG[A/G]GATATGAGGTATGAG | 70392 |
rs222455676 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95489189 | AAAGAAAACCAGTAT[C/T]AAGCACATGGAATGC | 70392 |
rs222459237 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95490698 | ATTAAAATGATCCAC[A/G]TGTTTCTTTAACAGC | 70392 |
rs222463835 | snp | A/T | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559523 | CTGTCTCTTTCTAAG[A/T]ACCAGGGGGCTGGGG | 70392 |
rs222595301 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95498491 | TCCCCCCATTTGCCT[C/G]CAAAACTCATAATGC | 70392 |
rs222597507 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95554015 | ACAAAATAAGGAAAA[A/G]TAAAATGTGTATTCA | 70392 |
rs222634334 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95517681 | TGCCTTATCCAACAG[A/T]AAGATTTCACCAACA | 70392 |
rs222667419 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95557304 | ATTAATAAGTACATA[C/T]TAAATGAATGAATAT | 70392 |
rs222747163 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95528058 | TGACTGAAAAAAGTC[C/T]AAAACTAGTAATCTT | 70392 |
rs222792831 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95549959 | ATAGCTTGAAACTAA[-/T]TTTTTTAAACTTTTA | 70392 |
rs222841305 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528895 | ATGACTGCTCTGGCA[A/G]GAGATCACATCTACA | 70392 |
rs222843226 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95537341 | GACACTATTGTGTAT[G/T]CCAACAAGTGCTTGC | 70392 |
rs222881161 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95555851 | TCAAGTTTTCCAACC[A/G]TCCCATTTCTAGTTC | 70392 |
rs222883123 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529540 | ATAATAATAACTATA[A/G]TGCTTTATCACACTA | 70392 |
rs222904000 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95487982 | TTTTTAGCATTCATC[A/T]ATAAATGAACCATTT | 70392 |
rs222960585 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536881 | TGTTTGTCCAAAAAA[A/G]CTTTATCAATGAAAC | 70392 |
rs223027459 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95526812 | AAAGTCCATAAGAGG[C/T]TGACAGATGTCCTTT | 70392 |
rs223035194 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95497968 | TAGGAATGGAAGAAG[A/G]AGAAGACTTCTTGAC | 70392 |
rs223035746 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95531336 | CTGTCTCGAAAAAAC[A/C]AAAAAAAAAAAAGAA | 70392 |
rs223058136 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95490348 | AAAGATCAACAATTA[C/T]AGGAACTAGATGAAA | 70392 |
rs223067540 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95533360 | TGCCAGTAGATGCCC[A/T]TATCTACATGTAGTG | 70392 |
rs223071284 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95522457 | TGTGAGTTTCAGGTC[C/T]AGTCTACAGATTAAG | 70392 |
rs223147440 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95530647 | ATATGGCCCTGTTTA[G/T]GTAATTTTTTCTGCT | 70392 |
rs223221666 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95484743 | ATCTTGGTTCCCGGA[A/C]ACCTCAGAGACTAGT | 70392 |
rs223232501 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95525853 | GAAGAGGGAGATTAG[C/G]GGGGGAATACAAGGA | 70392 |
rs223321045 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95536397 | TCATTGAAATGTAAA[-/T]AAAGAAAATATTCAA | 70392 |
rs223323402 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95530903 | CTCAAAGAACCACCT[-/C]TTGGTTTTGTTGATT | 70392 |
rs223350078 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95491915 | TGGGTCCTTTCTCTA[A/G]TGGATGCCAAGAAGT | 70392 |
rs223352501 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501066 | GGACCTAACAGATAT[C/T]TATAGACATTAGATA | 70392 |
rs223362794 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95492944 | CTGGAACCTAAAAAT[C/T]ACAGCAACATGCACT | 70392 |
rs223375790 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95534040 | TTTGAAATTTTATGA[A/G]GTACCATTTGTCAGT | 70392 |
rs223395067 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95503223 | AACTGAATTCTTCAC[A/T]GGGATAGAAAGAGCA | 70392 |
rs223443771 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95550699 | AAAACAACTGAGTTG[A/T]ACCAGCCAACCGGAG | 70392 |
rs223468181 | snp | C/T | | | utr-variant-5-prime | Asb12 | Mm_Celera | X:95495080 | TATCTTTTCACTTGT[C/T]GCTGCAGGCTGTGGA | 70392 |
rs223468699 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95500365 | AGAAGAAACCTTCCA[A/G]GGCTCTGCCAATTGG | 70392 |
rs223578560 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95549779 | TATCAGTATGGTCCA[G/T]AGCTGGATAGGATTG | 70392 |
rs223582081 | in-del | -/CTATAATCTGTATAACGGC | | | intron-variant | Asb12 | Mm_Celera | X:95508628 | CTTTCTCACTACAAT[-/CTATAATCTGTATAACGGC]CTATAATCTGTACTG | 70392 |
rs223660524 | snp | C/T | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559813 | TCGAACAGACGACCA[C/T]CTTGATGTAAAAGCA | 70392 |
rs223679887 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95496182 | AAAATTAGCCCTAAC[A/G]TGAACCCTATTCCTT | 70392 |
rs223751853 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95508856 | TTCAGCAAGTAAGTA[A/G]TGTTCTTCCAAGACC | 70392 |
rs223791011 | in-del | -/A | | | intron-variant | Asb12 | GRCm38.p3 | X:95525048 | TGGAATCTGAACCAG[-/A]AAAAAATTAAGTCTA | 70392 |
rs223859392 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95518078 | TTATTGGGTTGCTTT[G/T]TCCAGCTTTTGCCTT | 70392 |
rs223896466 | in-del | -/AAAAATT | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502083 | AGTTTCCTAACAATA[-/AAAAATT]AAAAATAAAAAATTA | 70392 |
rs223905585 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95511291 | TCCCCTACCCACCCA[C/T]TCCCACTTCTTGGCC | 70392 |
rs223922301 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95557425 | AACAAATATAGGGGT[A/T]TCAGAACTCAGAAAG | 70392 |
rs223930987 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95507526 | CATCTGTGAGGCTTC[A/G]TCTAAGCAGCTGATG | 70392 |
rs223936051 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95512100 | TGCAGCACTGATTTA[C/T]GGGTACAGCAGTATG | 70392 |
rs224014802 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95521868 | AAAACCTCTGATCAC[G/T]TTAACTGCTGAAAAG | 70392 |
rs224072775 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95516767 | TTATATTTACACAAT[A/G]GAGTATTATGCAAAT | 70392 |
rs224083609 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95517554 | AACCTAAGGCCCACA[C/T]CATGAGATGGAGCCC | 70392 |
rs224126619 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95506831 | TACTACTCAGTTATT[A/T]AAAACAATGACATCA | 70392 |
rs224137169 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95489431 | CTCTCATGTATCTCT[C/T]ACCTACTGCACCAAT | 70392 |
rs224138797 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95476041 | ATTAAGCCTGATCTT[A/G]ACTATTGATTTTGTT | 70392 |
rs224215164 | snp | A/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479471 | GGGAGGATTTGTAAC[A/T]CTTAATGGTTGCTAT | 70392 |
rs224235811 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95488387 | AATGGTCCACATTTA[C/T]TCTGTGAGATGGTGA | 70392 |
rs224266132 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95494925 | CTGATGTTATTTTAT[-/C]CTATTTGCTTATGTG | 70392 |
rs224272957 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95487668 | TCTAAAGCTGGTCTC[C/T]ACAGTAATGCTACTT | 70392 |
rs224273855 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95545763 | TTTCATGATAAAAAT[C/T]ATAGCATATATAATC | 70392 |
rs224299910 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95477896 | GTTCTTCCCTTTCTA[C/T]CTTCTAAGCACTCCT | 70392 |
rs224336189 | in-del | -/TAATCCCATACC | | | intron-variant | Asb12 | Mm_Celera | X:95499685 | GAAACAGTAAATAAA[-/TAATCCCATACC]GGGAAAGCCAAAAGA | 70392 |
rs224340789 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95554800 | CTCTATACTTATGCT[A/G]GAATCTTAATTTCTG | 70392 |
rs224343081 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95475671 | TATAGATGCATAAAA[C/T]CATTTAAGTATATAT | 70392 |
rs224349429 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95484821 | AGGCAGAAGCCACAC[A/G]GCTTCTGAGGCAGAC | 70392 |
rs224414882 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95544818 | CATAACACTGTTATA[G/T]CATGGTCCAATATTA | 70392 |
rs224525278 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95490617 | ACCAAGAGGCGAGTC[-/A]AGAAAGAGGAAAAAT | 70392 |
rs224547091 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95528672 | TCAAGTCCAGGAGAG[-/A]TCCTTTCAATAAATT | 70392 |
rs224551016 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95504982 | CAGCATGGCTAAGAT[-/AA]AAAAAAACCTCAGGT | 70392 |
rs224555818 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95552122 | TGAGGTTCTTGAGGG[-/A]GGTCTGCTGTCTTGT | 70392 |
rs224571360 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554149 | CTAATATCCCTGATG[C/T]CATGCCAGGAAACCT | 70392 |
rs224587759 | in-del | -/AC | | | intron-variant | Asb12 | Mm_Celera | X:95542275 | ATGATATCTGAATAT[-/AC]ATAGTAATAATCCCA | 70392 |
rs224654220 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95524636 | CAACTTTATTACACC[A/C]GTTTCAACATGAAGA | 70392 |
rs224679937 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95515215 | AAAAACCAAACAGTA[A/G]AAGGAAACAAATAAA | 70392 |
rs224691679 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95514337 | ACCAGGTGCATTGCC[C/T]ATAGACCTTCCTCAC | 70392 |
rs224720485 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95557639 | AAACGCTCAATACCC[C/T]GTTGAACAAGTGATG | 70392 |
rs224729354 | in-del | -/TTTCGAGT | | | intron-variant | Asb12 | Mm_Celera | X:95532476 | ATTATAATTTTTGTG[-/TTTCGAGT]TTCTTTTTAAGACAG | 70392 |
rs224735087 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95552739 | ATTCAGCCAGGTGTC[-/A]AAAGTATGCACAGTT | 70392 |
rs224768878 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95554388 | CAGTAGGAAAGCACG[A/G]GACACTCACCGAGTA | 70392 |
rs224772802 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95513247 | TTCAAACTCATGATC[A/G]TCCTGCTTCAGTCTC | 70392 |
rs224803087 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95548811 | TTTCAATGGTAGCAC[C/G]TGGGAGGCAGAGTTA | 70392 |
rs224840026 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95483180 | GAGGCCTTTGGTCCT[A/G]TGGAAGCTCAATGAC | 70392 |
rs224861039 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472751 | GCTAAGTAAAGTTTG[C/T]TCACCATAATTGTAA | 70392 |
rs224879843 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95556420 | GTTTGGGTTGGAAAT[A/G]CACTATTTTCTTGTC | 70392 |
rs224910545 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95523800 | TATCTCCATCCCTTC[A/G]ATGTAAACTTTATAT | 70392 |
rs224931390 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95516990 | ACTCTGGGCAGGTGG[G/T]GACAGGAATGGGAGG | 70392 |
rs224991758 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95553162 | CTTCCTCATCAACAG[A/T]GGCATGCTAACAAAA | 70392 |
rs225035350 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95516068 | TGACCACCACCATCA[C/T]TACCACTACCACCAC | 70392 |
rs225080036 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95518216 | AAAATGTAAAACTAG[-/A]AAAATGTATCAACCG | 70392 |
rs225108072 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95525188 | TATACAGGCTCAGCC[A/G]TTTAAACACTTGGTC | 70392 |
rs225118204 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95552441 | TGTCTCATTTGCCAG[C/T]CTCATTTCTGTTTTG | 70392 |
rs225134227 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95482522 | ATGCTGATTCTCATT[C/T]TGTCTTCATGAACAT | 70392 |
rs225162196 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95476804 | GCTGAAGTTCTCACC[G/T]AGACCACACAATGAG | 70392 |
rs225185588 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95525978 | AATGAACTTACCAAA[C/T]GGCTAGGGGAGACAA | 70392 |
rs225190022 | in-del | -/CCCCC | | | intron-variant | Asb12 | Mm_Celera | X:95498939 | CCAGCTGGTATGAGA[-/CCCCC]CCCCCCAATACATAT | 70392 |
rs225251663 | in-del | -/TGTA | | | intron-variant | Asb12 | Mm_Celera | X:95521093 | CCAAGAAAGCAGTAG[-/TGTA]TGTAGGTGGGTAGGT | 70392 |
rs225266887 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95522368 | AAACAAGGAAAAAAT[G/T]TTATTTTAAAATTTG | 70392 |
rs225302373 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95529920 | AGAAAATATGTTCAT[A/C]CAGGTAAATCAATTT | 70392 |
rs225317308 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95493932 | GTGGGTTGGTATCCA[A/G]GAGGGGACCTCCCCC | 70392 |
rs225359707 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95484509 | AAGAAGTAAAGACAT[G/T]GTGCCCATATGGACA | 70392 |
rs225478417 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95505605 | GAGGTTGGGGGGGGA[G/T]AGAGGGGAACCTGAT | 70392 |
rs225490042 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95549511 | GTCATGTGTCTCTGC[A/G]TTATTCACTGCCCAC | 70392 |
rs225490058 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536250 | GAGTAGGGCCCCTTG[A/G]TCCTGTGAAGGCTCA | 70392 |
rs225513132 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95553413 | GCTATAACAGAGAAA[-/C]CCTGTCTTTAAAAAA | 70392 |
rs225518999 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95521601 | TTGCATCTCAGTAAG[G/T]ACCAGAGAGAATAAA | 70392 |
rs225576993 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95536981 | TAAAGGGTTATAAAA[G/T]ATACGACAAAGGGCT | 70392 |
rs225611555 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95472790 | GGGTGAGATGGCAGG[A/G]TTTGCAAAGCTCAGA | 70392 |
rs225619251 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95533144 | TACATATATACCTTT[A/G]TACACATATATACAT | 70392 |
rs225652654 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95545421 | AGCATGTGCCCTTAA[A/G]CCCAGCACTTGTGAG | 70392 |
rs225653349 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95548935 | ATCTAAAGCTATATA[C/T]GACAGAGTATAACCA | 70392 |
rs225659788 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95530544 | GAATTCTGCACTAAA[A/G]CCATCTGGTCCTGGG | 70392 |
rs225706780 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95547134 | CAATGATATGGTTGG[-/T]TTAGCATATGTGTCC | 70392 |
rs225774061 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95498898 | GAGGTTGCTCTGACA[A/C]TGAGCCACCAACCGA | 70392 |
rs225777666 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95543478 | AAAGGTAAAAACATA[C/T]AGAAGGGAAACAGAC | 70392 |
rs225823283 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95544365 | CTGATGAAGGACTCA[G/T]GAACACTAGACTCCT | 70392 |
rs225823501 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95555135 | GACCACAGATTTGAA[G/T]AGTGCAGCCCCTTTT | 70392 |
rs225832008 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507287 | CACTTTCTATACCCA[C/T]GCTGGACTTCCAGTG | 70392 |
rs225876811 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507847 | GATCCCTTTCCCTTA[C/T]CTTGTTTGTCTTGTT | 70392 |
rs225898667 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554526 | AGCAAACACAGATGC[C/T]GGTGCTGTACATGGG | 70392 |
rs225901503 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95533805 | GATATGTGTAATTCC[A/G]TGTTATTTATAGATA | 70392 |
rs225920985 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95516159 | TCAATATAAATGGCC[C/T]CAATTCCCTTAATAA | 70392 |
rs225942777 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95514380 | GCATCAGTTCTCAGG[G/T]TTGCCTCTAACACTG | 70392 |
rs225947839 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95514455 | TCTTGTGGATTTCAC[C/T]GACGGTTATCCACTG | 70392 |
rs225948098 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95503588 | TCACTCTGCACAAAA[C/G]TCAAGTCCATGTGAA | 70392 |
rs225958662 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95517115 | GACTTTCTGGAATCT[A/G]TGAGGATGACCCTTG | 70392 |
rs225978552 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95503094 | AGAATTTGAAGAAGA[C/T]ATCAGAGGATGGAAA | 70392 |
rs225986208 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505096 | GAAATCAATCTGGAG[A/G]TTCCTCAGAAAATTA | 70392 |
rs226060709 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95513656 | TACTTAATTTGTAAA[C/T]GAGCCCATCATCATT | 70392 |
rs226111735 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95512983 | ATTGGGTAAGGTCTT[A/G]CCATGTGCGGCAGGT | 70392 |
rs226114336 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95542702 | TTTCACCTCTCAAAC[A/C]TTTGTGTCAGCATGA | 70392 |
rs226123494 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95475126 | CACTTCAAGAAATTG[A/G]CATTGACAATGATTT | 70392 |
rs226126886 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472046 | GTGTATGGCAAGGAT[C/T]CTATATCCATCTGGT | 70392 |
rs226141620 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472147 | AATGTGACATTAATG[C/T]CTAGGCCTGGCAGTT | 70392 |
rs226229897 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95470735 | TCTTTAACCTTTTCT[C/T]CACAGGGACCCCAAG | 70392 |
rs226262338 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95473231 | CTTTACACTAGGTCC[A/T]CTCCTTCAACTAACT | 70392 |
rs226277810 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95482222 | TCTTATTTGTTTGTC[G/T]TTTTGTTGTTGTTTA | 70392 |
rs226285651 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95541610 | AAGTCCACTGAAATG[A/T]ATAGACTTGGGTCTA | 70392 |
rs226288316 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95553308 | ACATGGTGGCACATG[C/T]CTTTAGTCCTATCAC | 70392 |
rs226348769 | snp | G/T | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95470147 | CAAACCCTTTCCCCA[G/T]TGGTCCTCTCCCACT | 70392 |
rs226372418 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95482849 | ACCAAACCAAGAAGA[C/T]ATTGTTGATGCTATG | 70392 |
rs226412684 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95487552 | ATGTTTCCTTAGGTA[-/C]CCCCACCCCTTCTAA | 70392 |
rs226502163 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95552292 | ACAGATTGAAATTCT[A/T]TAATGAAAAGGAGAA | 70392 |
rs226514889 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95512014 | CTACGACTTTCTTCA[C/T]ATTGTCCAATTATGG | 70392 |
rs226556969 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95534415 | TCTGTCATTGTACAA[A/G]TACCATGCAGTTTTT | 70392 |
rs226560006 | snp | A/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502315 | GTTGTTCATGAAAAC[A/T]TTTGAAAAAAGTATA | 70392 |
rs226658582 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498100 | CTGGGAGTTTCTCAC[C/T]TTCCCGGTCTCTGGT | 70392 |
rs226678935 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95542125 | TTGCCCCTGTTTCTG[C/T]GGTTGTATCACAAAA | 70392 |
rs226682583 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95496845 | TCTGGAATTAGCATT[C/T]GTCAAAGCCCTAAGC | 70392 |
rs226698200 | snp | G/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95510143 | AATAGTTTAACTACA[G/T]TACTTCTCAGAGAAT | 70392 |
rs226721208 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95506314 | GATCAGGTGAGGTGG[G/T]GTGGGGATGTTGACT | 70392 |
rs226743529 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95497510 | GAACCCTGGCAATAT[A/G]GCACTGCCAGAACCG | 70392 |
rs226761723 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95542858 | ACTATTCATCAGTCT[A/G]TGGCAACTGCTGAAC | 70392 |
rs226829596 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505187 | GCCAGAGAGGCACAT[A/G]TTTCACTATGTTCCT | 70392 |
rs226831226 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95551060 | TTCTGAAAAGGACTC[C/T]AATAGAATAGGAAAT | 70392 |
rs226843122 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95480655 | TAAACCTGCCTACAC[A/C]AATCTCCAAAAATTC | 70392 |
rs226927159 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95519591 | GGACAGTTTACACTG[A/G]CCACTAAATCAGTAA | 70392 |
rs226935494 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95540006 | GTCAATAAGGTAAAA[C/T]AGCAACCAACCAACA | 70392 |
rs227109034 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95548433 | TGACACAAGGCAACA[A/G]CTGCTTAACTGATAG | 70392 |
rs227118853 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95476554 | GATGTATCCTACCAG[A/T]GCTTGAAATAAAATC | 70392 |
rs227251455 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95520439 | CAGTGTGTGGCGGGG[A/G]AGGGGGTCATTGCAA | 70392 |
rs227294180 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95509617 | GTGACTAAGGTCAAC[A/T]CTTGGGGATACTTTA | 70392 |
rs227299196 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95480685 | TTCAATTAAAGGCCA[-/TT]TTTTTTTCTACTGTC | 70392 |
rs227373143 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95530685 | TAACTTAGGTACATA[A/G]TATTTGTCTAGAAAT | 70392 |
rs227433266 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531702 | GACAGGACATCAAGT[A/G]GAGGGATGGGGTTGT | 70392 |
rs227441784 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95474839 | TCTTAACAAAGGTGC[-/AA]AAAAAAAAAAAAAAA | 70392 |
rs227480249 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95477320 | ACTACTTGCCACCTA[C/T]ATTCATCTTAGAAAA | 70392 |
rs227482769 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95532790 | TGTTGCATATAGATA[A/T]ATAACATGAAACGAA | 70392 |
rs227485088 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95543785 | TCCCCCCCCCCCCAC[C/G]CTTGGTGCCATTTCT | 70392 |
rs227489465 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95540847 | TCTTAGAATGGGGAC[C/G]AAAATACTCATGGAC | 70392 |
rs227499643 | in-del | -/CTT | | | intron-variant | Asb12 | Mm_Celera | X:95552099 | CTCTCTCTTCCTCTC[-/CTT]CTTCTTGAGGTTCTT | 70392 |
rs227509571 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95541028 | CTCTCCTGAGAGGCT[C/T]TGCCAGTGCCTTGCA | 70392 |
rs227576928 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558920 | ATAGCTCAGAAAACC[A/G]TTGTTTCTTTAGACA | 70392 |
rs227578358 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95533514 | TTCACAATCATGGTA[A/G]GGAACATCAAGGCAG | 70392 |
rs227589332 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531079 | AAATTTCTTTATCAG[A/G]ACACTTAGTGCTATG | 70392 |
rs227622325 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95552654 | AATCATTAAAAAAAA[-/T]ACTACAGCATAGAGA | 70392 |
rs227660944 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95500408 | GAAACTGCAAGAAGC[A/C]ACCAGAACAGCACCA | 70392 |
rs227663808 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95538128 | AATGAAAAGGGAGAT[A/T]AAACAACAGAATCTG | 70392 |
rs227664258 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95543079 | AAGTATCACTTTAGC[A/G]AAAGTTTTTACCTTC | 70392 |
rs227679633 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95549388 | TTTGCCTACTACTAT[C/T]TTTCCTCTCCCTCTT | 70392 |
rs227721464 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95518463 | CTATTGAAATCCTTA[-/T]TTTTTTTTCCTCTAC | 70392 |
rs227759673 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95495193 | GATAAATGTCCTTAA[C/T]TTGGTTGTTGTTGAG | 70392 |
rs227761527 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95492099 | CTCTCTCAGTAAGAA[C/T]TCTAATAGTACTGCT | 70392 |
rs227770820 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501805 | GCTCCAGGACAGCCA[A/G]GGCTATACCGAAAAA | 70392 |
rs227781648 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95499820 | CTACCACCACCAACA[A/C]CAACATCAATATAAC | 70392 |
rs227812657 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95509824 | TAAGAGGAAATAAAG[C/T]CACCCACTTTGGTTC | 70392 |
rs227816340 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502479 | TATAAACAGAAGGGG[A/G]AAAACTACACAGTCA | 70392 |
rs227827894 | in-del | -/AATAAATG | | | intron-variant | Asb12 | Mm_Celera | X:95519153 | ATAAATAAATAAATA[-/AATAAATG]AACTAAGCTAAGAGA | 70392 |
rs227838565 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500672 | TTCCAGAAAACACTA[C/T]GTGTCTGTTCTCGGC | 70392 |
rs227840745 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95494645 | CCCACAATGTAGCCA[A/T]AGTCTGGCTACACAG | 70392 |
rs227850265 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95503290 | ATAGTGAAAACAATC[C/T]TGTACATTAAAAGAA | 70392 |
rs227909089 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95508884 | ACCTTTGCTTCATTT[C/T]CTGCCTCCTCCAGGT | 70392 |
rs227961555 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95530039 | AATTTGAACTAGTAT[A/T]CGTCTAGGCATTTAG | 70392 |
rs227997324 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95507997 | GGTGAGAGAAGGGAA[A/G]GGGCTGCAATTGAGA | 70392 |
rs228011603 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95553674 | TACTCCTATATTAAG[C/T]AAGCCATTTTAGCAC | 70392 |
rs228151954 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528981 | GTATGATCTGTGTAA[A/G]GCACCCTTTACTATC | 70392 |
rs228207572 | in-del | -/TTAT | | | intron-variant | Asb12 | Mm_Celera | X:95557202 | TGTATCTATCATCTG[-/TTAT]TTTTTCTTTCTGTCA | 70392 |
rs228231013 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95523875 | GTTTTCCTTTTGGAT[A/T]TTTTTAGACAAGAGT | 70392 |
rs228299553 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95497694 | GTGAAGAAAGAGAAT[-/A]AAAATAGTTCGAGAC | 70392 |
rs228325050 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95531903 | CAGCTAGGAGTCTAG[C/T]ATGGCTGTCCTCTGA | 70392 |
rs228340058 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95495349 | AAGGCCTACCCACAA[C/T]CATAAGCATAACCCC | 70392 |
rs228374768 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95483656 | GAACCCTGGAAAGGG[C/G]TTCCAGGTAGATCCA | 70392 |
rs228374947 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95496591 | AGTCTGAATCCCAGC[A/G]CAATCATAGCCTTAA | 70392 |
rs228385398 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95547257 | GTCTAACTTAAAAGT[G/T]ATAAATGACACAAAA | 70392 |
rs228388976 | in-del | -/ACT | | | intron-variant | Asb12 | Mm_Celera | X:95532888 | AAAAGGGGGTATTAA[-/ACT]ACTAACTACTTTTCA | 70392 |
rs228422554 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95481399 | TGACAATTTCCAAGA[-/T]TTTCCCATGCTAAAT | 70392 |
rs228451324 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95522826 | TATATAATAGTCAAG[G/T]TATTAGAAGTTAATG | 70392 |
rs228453896 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95532543 | CAAGTGTTGGGTTTA[A/G]TGGCATATGGGATTA | 70392 |
rs228508992 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95535085 | TTGTAGGCAAATACC[C/T]GGGGATCCATCCCAT | 70392 |
rs228513172 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95482679 | ACTCTTTAAAATATA[A/G]AAACATGACATCAGT | 70392 |
rs228519344 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95499702 | GGAAAGCCAAAAGAT[A/G]AGAAGCATGGCACAC | 70392 |
rs228655839 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95556925 | CATCTTCCATTACTC[-/TT]TTCTTTTTTTCTTTG | 70392 |
rs228683596 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95481644 | CTTTGGCATGTTATA[G/T]CAGAGCTTGAAAACA | 70392 |
rs228684675 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95494315 | TGATAGGTGGGTGGT[C/T]TTTTGGTAGGTTGCT | 70392 |
rs228694310 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528310 | GAATCCTAGATAGTG[A/G]CTTTAGAAAAACAAC | 70392 |
rs228695491 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95506421 | GAGACTAAAAAAATA[A/T]TAATAATAACCATGT | 70392 |
rs228766488 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95493185 | GTGGGATGAGGAAAG[A/G]GAGCTCATCTCTAGG | 70392 |
rs228767115 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95497536 | AACCGAGATATTCTA[C/G]CACAGCAAGCCTTGG | 70392 |
rs228789998 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95515079 | AGGAAATGAATAAAT[-/C]CCTTAAAGAAACTCA | 70392 |
rs228824550 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95521699 | TGAAACTTCTAACTC[G/T]GATTCTCCCCAAAGC | 70392 |
rs228825670 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95536128 | ATCAACCAACCAGAC[A/C]CCCAAGAGCTCCCTG | 70392 |
rs228926435 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95521029 | AAAAAAAAGCAAAAA[A/C]TGGGCTAGTGAAGTA | 70392 |
rs228962186 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95538703 | AAGGAAACTCAAAGG[-/A]AAAAAAAACACATGA | 70392 |
rs228990625 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529217 | TGGGACAGTTTTACA[A/G]AGACAGGTGGTAGAC | 70392 |
rs229026259 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498204 | GCTTCAGTCCTGTTC[C/T]CCCCAATACCTGATC | 70392 |
rs229070538 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95529944 | TCAATTTATTTAAGA[A/T]AATATTAATACAGGT | 70392 |
rs229090484 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95521916 | ATTCACAGGACCGAG[-/T]TTTTGCTAATGTTAA | 70392 |
rs229120895 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95533567 | GGAACAGTAACTTAT[C/G]GCTTACTTCCGGATA | 70392 |
rs229138505 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95473127 | CTACAAGACAGAAAT[A/C]GTAACCCATGCTTCC | 70392 |
rs229210372 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559634 | CCTTGGTTGGTGAGA[A/G]CTGAGCTGTTGGTGA | 70392 |
rs229217883 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95507077 | GAAAGTGGATGGAGA[A/G]TGAGAACTGAGTGAA | 70392 |
rs229229861 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95490738 | CTATATTTAATCATA[C/T]TTGATTAAATATAGA | 70392 |
rs229253905 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95499028 | TAGAGATTTGAAGCC[C/T]CAGGGAGTGGGGAGA | 70392 |
rs229311172 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95499493 | TACCTTGCAGACATA[A/T]GAGAATATAAATGTC | 70392 |
rs229402464 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95534202 | TTGATCCACTTGGAC[A/T]AGGGCTTTGTACAAG | 70392 |
rs229458550 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95528139 | AAAAGAGATGGTAAC[C/T]TAAAAGAGATTTATA | 70392 |
rs229524522 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95535049 | GGGTTATAAAAGGTA[C/T]GACGAAGGACTTGAT | 70392 |
rs229543761 | in-del | -/TC | | | intron-variant | Asb12 | Mm_Celera | X:95556064 | AGGCTCCTGTTTGTT[-/TC]TGTTTCCTCAGAACT | 70392 |
rs229547236 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95477525 | CTTCACCTTCTTTAT[C/T]CCAACTTGAGAAACT | 70392 |
rs229582663 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95474905 | CCAAAAACCAACCAA[A/C]CAAACAAACAAACAA | 70392 |
rs229599245 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95545070 | CATATATATGTATAT[A/G]TGTTAAGTAATGATA | 70392 |
rs229602281 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95527363 | ATGGAAAAACTAAGA[A/G]AATAAGAAATAGACT | 70392 |
rs229602282 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536025 | TCACAGCCAACCATT[A/G]GACTGAGCACAGGAT | 70392 |
rs229603085 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95512405 | GGTAGTTTGTTTATA[-/TT]TTTTTTTAATTTTTG | 70392 |
rs229725516 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95509159 | CTAGCCTTATCCTTA[G/T]CCTAATATTGTCCTA | 70392 |
rs229777186 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529147 | CAGGAGAACAAACAA[A/G]GAAAGGCCAGTTAAG | 70392 |
rs229792834 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95520315 | CCCACGATCTCTAAC[C/T]TGTCAAGCCTGAATA | 70392 |
rs229896996 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95518697 | TCGCAGTTGCTTGTG[C/G]GACTCCATCAAGAAC | 70392 |
rs229901492 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95556655 | GACTCCAAATCTAAT[A/C]ATTTTTCAACTTGCA | 70392 |
rs229947384 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95477043 | GTGACACTGATAGTG[A/G]TAAAGTCAAAGACTG | 70392 |
rs229950759 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95488530 | AATGTAATGCATGAG[C/T]GTCATATGACACCAA | 70392 |
rs230057760 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95489509 | AATGTTCAAGACTGT[A/C]AGCAAGCTCCCAATT | 70392 |
rs230069408 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95476328 | CACCTTAGAGATAGG[A/G]AATTTGAAGATTAGC | 70392 |
rs230079884 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498283 | CTCCCTCGCCCCACC[C/T]CTGTGATTGCTTTCT | 70392 |
rs230101898 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95502867 | AACTCCTACAGCTGG[-/A]AAAAAAAACCTTTAT | 70392 |
rs230122200 | in-del | -/AAA | | | intron-variant | Asb12 | GRCm38.p3 | X:95524996 | GGTAAAGTTCTGTTT[-/AAA]AAAAAAAAAAGGCCA | 70392 |
rs230140494 | snp | C/T | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558482 | AGGAAGAAATTCAGA[C/T]CTTACTGGCAAGAGA | 70392 |
rs230140515 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95548175 | GCCTTTGATAAAGTT[A/C]AATATCTGAGGATAG | 70392 |
rs230156330 | in-del | -/CACACACACACA | | | intron-variant | Asb12 | Mm_Celera | X:95499750 | GTGTGTGCACTCATG[-/CACACACACACA]CACACACACACACAC | 70392 |
rs230174338 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95549310 | TCACAGATGCTGTGT[A/G]TTCATGACTACAAAA | 70392 |
rs230207911 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558088 | AGTAACTCCTGCTTC[A/G]AAATCACTAACAGTC | 70392 |
rs230214600 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95557486 | TGTATGAGAAAACAG[-/A]AAAAAATGTTAGGTT | 70392 |
rs230224752 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95500167 | AAATGTTTTAACCTT[-/C]CTTCTAGCCCACCAG | 70392 |
rs230246738 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95557266 | CTGAAACAAGCCTAG[C/T]TTACAGTAGTTAATA | 70392 |
rs230304920 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95517303 | ACTGACAGAAGAGCC[A/C]TATTTCCAAGGACAA | 70392 |
rs230310829 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95526023 | CATCATTTTCAGCTA[C/T]GAGAAATGTCTAGTG | 70392 |
rs230386146 | snp | G/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95527295 | GGAGTTTTATCATAT[G/T]CTCAAAGAGTTATGT | 70392 |
rs230400515 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95527484 | CCTCTAATTCAAATC[A/G]GGCAAATTCTTAAAC | 70392 |
rs230402605 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95516513 | GCTGCTGAGGATGTG[C/G]AACAAGAGGAACAGT | 70392 |
rs230440368 | in-del | -/GGG | | | intron-variant | Asb12 | Mm_Celera | X:95491833 | GTCCCTGGGAGCTCT[-/GGG]GGGGGGGGTCTGGTT | 70392 |
rs230546782 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95526538 | AAAATGGTTAGAACA[C/T]AGGGCTTAAAACAAC | 70392 |
rs230554669 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95534367 | GTGTGGGTTCATTTC[C/T]GGATCTTCAGTTCTA | 70392 |
rs230557030 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95487470 | GGGGGACTTTTGGGA[C/T]AGCATTTGAAATGTA | 70392 |
rs230557360 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95473788 | TGAACCCAGGGTTTC[A/G]TGCATGCTAGACAAG | 70392 |
rs230564108 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554697 | GCCAGCAATAGCCCG[C/T]TGTAGCTTCTCTGAT | 70392 |
rs230595127 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95555325 | TGTCTACTGCCATCT[C/T]TCTAGTTAAAACCTG | 70392 |
rs230611053 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95475375 | CCTCATGGGTACATA[C/T]GTTAAGGACCCTAAA | 70392 |
rs230634433 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95484595 | ACATGTTCATAGTAA[A/G]CCGGCTCTAGTACAA | 70392 |
rs230642576 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95508799 | GGTCCTGAGTTGTAT[-/AA]AAAAAAAAATGTAGG | 70392 |
rs230724171 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95496791 | GCATGAGCCCTAAAA[C/T]TAATAATACACACAA | 70392 |
rs230734917 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95484709 | AACAAGAAATGTTTC[C/T]GGAGCACCTGGGGGA | 70392 |
rs230777312 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95497324 | CTGGGAACATACAAT[A/T]TCACCTGAGGCAAAG | 70392 |
rs230789108 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95485110 | TGTGCACCTTCCCTG[C/T]AAGAGAAGAGCTTGC | 70392 |
rs230811276 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95514249 | TTAAAAATACGAGGA[A/G]GAAGGAAAAATGATT | 70392 |
rs230844794 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95524190 | GGTCACATTAAATTC[C/T]TGTTTTGTTCTATAC | 70392 |
rs230850689 | in-del | -/TAACC | | | intron-variant | Asb12 | Mm_Celera | X:95542561 | TCCACTGGACCTTCT[-/TAACC]TCTATGCAGGCTTGC | 70392 |
rs230857963 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95514697 | TGGATCCCTCAGAGC[A/T]TCTCCCACTGGCTTC | 70392 |
rs230888573 | in-del | -/TCACAA | | | intron-variant | Asb12 | Mm_Celera | X:95483538 | CCCTCGGATGCTAAG[-/TCACAA]GGTTTGGAGGCACCA | 70392 |
rs230889605 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95544750 | ACTTAGCAAGCTTGA[-/T]TAGATCAAGGAAGTA | 70392 |
rs230949682 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95532664 | CATTTCTTATAATTT[C/T]ATACATGAGTTCTAT | 70392 |
rs230964337 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95524420 | AACTGTAGGTATGTA[C/T]AGGATGCCTTTTATA | 70392 |
rs230971308 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479743 | AGAAAAAAGAGAAAA[-/GAG]GAGAAGAGAAAAGAA | 70392 |
rs230974870 | in-del | -/AAAAAA | | | intron-variant | Asb12 | Mm_Celera | X:95510890 | TAAAAACAAGTTCAT[-/AAAAAA]AAAAAAAAAAATCAG | 70392 |
rs231009155 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95551613 | GTTTGTTTGTTTGTA[-/T]TTTTTTATCCTTTCA | 70392 |
rs231115444 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507431 | GCCCAAATTGAACCC[C/T]ACCCCATGGGATAGA | 70392 |
rs231140824 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95524901 | GGAAGAAAATTCTAG[C/T]AAGGATAAACCAGTA | 70392 |
rs231166971 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95494513 | CCCCCTTTCTTACTA[C/T]GAACTTTATTCAGTG | 70392 |
rs231190301 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95523437 | TCCTTTCTCCTACCC[C/T]GAGGTTCAGTTTCTT | 70392 |
rs231275170 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95502424 | GAAGTAGGCTTTATC[C/T]TAGAGATACAGGGAT | 70392 |
rs231306404 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95476153 | TTCCTATACTATTTT[C/T]CTTCTATTTCCTCAC | 70392 |
rs231316188 | in-del | -/GGGC | | | intron-variant | Asb12 | Mm_Celera | X:95505600 | GGGTGAGGTTGGGGG[-/GGGC]GGGAGAGAGGGGAAC | 70392 |
rs231349926 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95475254 | ATAGAGTGATGACAC[A/G]TTTTCAGAATGGCAG | 70392 |
rs231435359 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95531976 | AGCCAATGGACAGAA[C/G]TCGGGGACTCCTGTG | 70392 |
rs231476256 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95485389 | CCAAAAAGGTAGACC[C/G]GGATTTAAAAGCATA | 70392 |
rs231476516 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95545470 | CTGTGCATTCAAGAC[C/G]AGGATAGTGTACAAA | 70392 |
rs231595637 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95535454 | ATCATTACAGGGGAA[C/T]GAACACCAGGGCCAA | 70392 |
rs231601096 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95514622 | TCAATTCTCAGGGTT[G/T]CCCCTAGTTCTGAAA | 70392 |
rs231660307 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95493338 | GCAGAACTCTCAGTG[G/T]AGGGATAAGGACACC | 70392 |
rs231697875 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95545656 | TTCAGGAATATTCTT[A/T]TATACAAATAATGAG | 70392 |
rs231707312 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95525161 | CTATGATGGCTTAAA[A/G]GAAAGATGTCCTATA | 70392 |
rs231734891 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95488299 | TTTGGTCTCACCTGC[C/G]TAGGCCATAAGTACC | 70392 |
rs231740432 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95534715 | CTGAATCACAAAAGA[A/G]CAGACATGGTGTACA | 70392 |
rs231750704 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95475890 | TTAAATTATACTAAT[C/T]ATTGATTATTTCCTT | 70392 |
rs231772365 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95546286 | GCACTGGCATAGCCT[C/T]ACAAGAGAGAGCTAT | 70392 |
rs231899029 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95483603 | TCAAGTCTATTTTTT[C/T]GTTTTCCTCCACCAA | 70392 |
rs231902727 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95555910 | TTGAGATAGTGAAAA[A/T]GGTTTGTGAAGGCTG | 70392 |
rs231912620 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95472271 | TGACATTTTTGATTA[A/G]TTTAAACTTCCGCAC | 70392 |
rs231922616 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95553778 | TGGACTTTTTAAAAG[A/C]GTGATGACCAAATTC | 70392 |
rs231929642 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95542495 | AAACTACATATTTAA[A/G]GGTTCTGAAATATAA | 70392 |
rs231930934 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95505296 | TTCACTTACAAAATG[A/G]AATTCTACTCAGCTA | 70392 |
rs231955802 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95543346 | TCTGAGTATGAACTC[G/T]GGACCCCACATAGTA | 70392 |
rs231970205 | in-del | -/AAAAAA | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559483 | AGACCTGTAAATATT[-/AAAAAA]AAAAAAAAAAAAAAA | 70392 |
rs231990926 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95506495 | TGAGATTCTTCCTTA[C/T]TCCCATGAGAATGGC | 70392 |
rs232028296 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95553521 | AGAAGAAGAAATATC[C/T]TTCTTCATACTAAAT | 70392 |
rs232030786 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95553020 | TAGGCAATAGGAATG[G/T]ATGTAAATTAATCCT | 70392 |
rs232062865 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95525919 | TATGCAAACTTTCTA[C/G]TCTAGAAGCTTCTTA | 70392 |
rs232080976 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95512699 | CAGTGCTACACGGCT[A/G]TGAAGTCAGAGTTCA | 70392 |
rs232086568 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95542528 | AAAATAAAAAAAATC[-/A]AAAATGATGGTGCAT | 70392 |
rs232091829 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95514881 | ACCCAGAATACAGCT[C/T]CCAGACCTATAATCA | 70392 |
rs232103730 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95515873 | GAGAAAATAATATAT[C/T]CTATGATAAAGTCAA | 70392 |
rs232114299 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95502887 | AAAACCTTTATTTAA[A/G]TGACTGGATACAAAA | 70392 |
rs232144541 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95522619 | AGGAGGCAGATTTCT[A/G]TGAGTTCCAGACAAA | 70392 |
rs232178008 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95512422 | TTTTTTAATTTTTGG[C/T]TTTTGATGGGAAGAG | 70392 |
rs232181738 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95511824 | ATCAGGCTCTGTGAG[A/T]TCCTGTGTGCATCTG | 70392 |
rs232312088 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95473047 | TTTAACTCAGCTCTC[C/T]AAGATCCTAACAAGG | 70392 |
rs232322316 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95514315 | AAAACTAGATGAATT[C/T]CACAAAACCAGGTGC | 70392 |
rs232335952 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95505437 | TAAGTGGATATTAGC[-/AA]AAAAAAAAAAATACA | 70392 |
rs232378204 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95481786 | AAAGTTTTTAACTAT[A/G]ATTATTCCTCATTTC | 70392 |
rs232392763 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95524306 | AAATCATAAAATCAA[G/T]TACCCCTCCCAAGGA | 70392 |
rs232403836 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95472667 | AACTCCTCTTCTCTC[C/T]GTAATCTTTACACCT | 70392 |
rs232446944 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95493070 | AGACAATAACTAACT[A/T]ACTAACTAACTAATT | 70392 |
rs232458176 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95481440 | AAAGCCTTTTTAAGG[G/T]TTTATAGTTCCTTTG | 70392 |
rs232460617 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95484136 | TCTCTTTTTCTTTGC[A/G]ACAAGAAGTCCAATT | 70392 |
rs232475200 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95551471 | GTGAAAGAGGAGGAA[C/T]CCCCATTCACTGCTG | 70392 |
rs232505167 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95480418 | TATGCGTACATCCAT[A/T]TGTTAGGAAAGAAGA | 70392 |
rs232549375 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95471725 | ATCTGAGGGCAACAA[A/G]AAAGAGGGGGAAAGA | 70392 |
rs232581199 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95552622 | AAACAACTTTACAAG[A/T]TAAGAACTATGACAA | 70392 |
rs232586256 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95525590 | TTAGGGTAAATGGAT[A/G]GAGGAAAAAAATCAT | 70392 |
rs232625428 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95482931 | CCAATACAGCTGTGG[A/G]TGCACATAGCCAATC | 70392 |
rs232655070 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95533138 | AACAAATACATATAT[A/G]CCTTTATACACATAT | 70392 |
rs232661625 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95483094 | ACCACCAAAAGAGTA[C/T]ACATGGTGGGACTCA | 70392 |
rs232686944 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95533763 | TCACCACCATAATTT[G/T]TTTAGGTGATGAAAA | 70392 |
rs232729903 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95520921 | TCAAGCACTGCTCTG[A/T]TATTTTAATTTTTCA | 70392 |
rs232731671 | in-del | -/A | | | intron-variant | Asb12 | GRCm38.p3 | X:95510121 | CAAAAGTTCCTTAGG[-/A]AAAAAAAATAGTTTA | 70392 |
rs232776720 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95476203 | TACAGAAGAAAATAG[-/AA]AAAAAAAACTGTAGT | 70392 |
rs232778083 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95511539 | CTCAGGTCTTAAAAA[C/T]GCCAATATAAAATAA | 70392 |
rs232788489 | in-del | -/GGGGGGG | | | intron-variant, upstream-variant-2KB | Asb12 | GRCm38.p3 | X:95478256 | AGTGTGTGTGTGTGT[-/GGGGGGG]GGGGGGGGGAGCTGC | 70392 |
rs232804479 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95503674 | AAATATCCACAAACA[A/C]ATTGCCACAGAAGAC | 70392 |
rs232810128 | in-del | -/G | | | intron-variant | Asb12 | Mm_Celera | X:95476770 | TTCTTATTTCATTTT[-/G]GGGACTCGGAGCAAA | 70392 |
rs232813624 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95494847 | TTCAGTTATCAAGTA[C/T]GGTTTATAAAATCAC | 70392 |
rs232867497 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95495612 | AGACCTAATCCTAAG[A/G]ATAGCTTCAAATCTA | 70392 |
rs232885758 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95513372 | TTTACTGTGATAAAT[A/G]CACTATCCTAACAAC | 70392 |
rs232905440 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95503058 | AGACCTGTATGACAA[G/T]AACTTTAAGTCTCTG | 70392 |
rs232913161 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95522035 | ATTATAGAAAAGCCC[A/G]GTAAGATCAGAAAAA | 70392 |
rs232918974 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95503353 | CTGAATTATAAAGCA[A/G]TGGTAATAAAAACTG | 70392 |
rs232948828 | in-del | -/G | | | intron-variant | Asb12 | Mm_Celera | X:95489730 | AATTGGATACAATTA[-/G]ACTCTAATAACATGA | 70392 |
rs232951169 | in-del | -/C | | | intron-variant | Asb12 | Mm_Celera | X:95512820 | AAAAAACAAAAACAA[-/C]CCCCCCCCCAAAAAA | 70392 |
rs232993280 | in-del | -/GGA | | | intron-variant | Asb12 | Mm_Celera | X:95536365 | GGTTTCTGGGGGGGG[-/GGA]ACCAGGAAAGAGGAT | 70392 |
rs233189376 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95479900 | GAAGAGGAAGAGGAA[C/T]GGGAGAAGGCTGTGA | 70392 |
rs233189866 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95470587 | CTGTCTCAACCATCT[C/T]CCAAATGCATGATAA | 70392 |
rs233204074 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95541977 | GGGCCAGAAATGCCA[G/T]AAGGACAGACCGCTT | 70392 |
rs233216846 | snp | C/G | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95470110 | AGGGCCAGATGTATG[C/G]TCTTCCTTTCCTATG | 70392 |
rs233220479 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95541381 | TGGGGAGCAGGGGGA[A/C]GGGGAGGGAATAGGG | 70392 |
rs233310730 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95552492 | GGTTTGTATCTCTTA[C/T]TATTTAATTAAGGCA | 70392 |
rs233320264 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95550868 | GACCTGAGTTCAATT[A/G]CCAGCATTCATTTAC | 70392 |
rs233357461 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95492310 | TTTTGCTAGCTCTGA[A/G]GTAGTTAAAATGTCT | 70392 |
rs233363407 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95550785 | ACAGAAATTACACCT[A/G]AAGAATAAGTTACTT | 70392 |
rs233366678 | snp | A/C | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501560 | GGCCTGAGATCAATA[A/C]ATTAGAAACAAAGGG | 70392 |
rs233474024 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95510975 | TTTCTATATTTGGCT[A/C]GGAGAAAATGTGAAT | 70392 |
rs233514942 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95530151 | GAGGGGGGGGGGGCA[G/T]AACTTGACTTTCTTG | 70392 |
rs233521402 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501839 | TGTCTCAAAAAACTT[-/AAA]AAAAAAAAAAAAAGA | 70392 |
rs233524080 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95519961 | TATGATCTTACAGCA[A/G]TCAGGATGGAGGTCT | 70392 |
rs233676198 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95504920 | AAAGTCCCTAGAGAT[C/T]AGAGAAATGCAAATC | 70392 |
rs233724429 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536651 | GGCTGGAAAAAAAGA[A/G]ACATTTTTGAGCAAA | 70392 |
rs233727661 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95550003 | CTTGAATTCCTGGTC[C/T]TTCTGTCTCCATCTC | 70392 |
rs233745503 | snp | G/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95478787 | CTTAGTCAAATCACA[G/T]GTTTTAAGTGTATAA | 70392 |
rs233759453 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95537274 | TGAAAGAATGACCAT[C/G]CAGAGACTGCCCCAC | 70392 |
rs233762657 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95550533 | ACTGTTTTACAAAGA[C/T]AGGTTGTAGGTGAAC | 70392 |
rs233827519 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95549345 | TGACATATCCAATAG[A/G]CAACTATTCATAGTG | 70392 |
rs233843933 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95549011 | AAACCTGGAATAAGA[A/G]TGCTCATTCCACTCT | 70392 |
rs233877963 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95508095 | GGGGATGACTCAGTA[C/G]AGTATTTGCAACACA | 70392 |
rs233889463 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95498502 | GCCTCCAAAACTCAT[A/G]ATGCCCTCTTACTTA | 70392 |
rs233897731 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95512600 | AATTGATTAGATACA[C/G]AGGTTGGGATGTAGC | 70392 |
rs233936699 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95508748 | TGATTAATGATTGAG[C/T]CAGCCCATGGTGGGG | 70392 |
rs233945093 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95499179 | TAAAAAAAGAGGAGA[C/T]AACTGCCAGCTCCAT | 70392 |
rs233949342 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95558276 | CCAACCTTCTAGGAA[A/G]CTTTTATTCACCAAA | 70392 |
rs234010879 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507333 | TATCCACCCACAAAA[C/T]ATCAACCCCAATTTT | 70392 |
rs234107984 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95552899 | ACATAAAGAGTAAGC[C/T]GATTCCAACAAGAGA | 70392 |
rs234116647 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95517202 | GGCGAGGCTTCCAGT[G/T]GTGGGAGTGGGTTAC | 70392 |
rs234155619 | snp | A/C | | | downstream-variant-500B | Asb12 | Mm_Celera | X:95469766 | GTTTTCATGGGTCAA[A/C]CAGAAAATATGTCTC | 70392 |
rs234241030 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95522212 | TTTGAAATTTTCATT[C/T]AGAGACACAAAAATA | 70392 |
rs234245374 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95474877 | AACAAAACAAAAAAC[-/A]AAAAAAAAAACCCCA | 70392 |
rs234278814 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95532033 | GTTGTGGAGGAGGGC[A/G]ACCCTATAGGAAGAC | 70392 |
rs234284761 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95551738 | CTTTCAGAAAAGGCA[A/G]GCCTCCCATGGATAT | 70392 |
rs234286043 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500874 | GTTCTGAACATCTAT[A/G]CCCCAAATACAAAGA | 70392 |
rs234332859 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95541230 | AAAAAAAAGTGGAGG[G/T]ACTTGTGTCTCTAGC | 70392 |
rs234343913 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95492710 | ATAAATTAAAAACAG[C/T]GCATCTCATAATGTC | 70392 |
rs234356625 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95541540 | CACAATTTATGATAA[A/G]TATAAATCCAATGTG | 70392 |
rs234397799 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95531291 | TCTACAAAGTGAGTT[C/T]CAGGACAGCCAGGGC | 70392 |
rs234397800 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95542253 | GGCTAAGACAGAATG[C/T]CTAAACATGATATCT | 70392 |
rs234402804 | snp | A/G | | | intron-variant | Asb12 | GRCm38.p3 | X:95493500 | GTGACACTATTAGTA[A/G]TATTCTGTTATGCTT | 70392 |
rs234424825 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95518891 | GATTACCTAAGTTTG[-/A]ATCTTGGGATCCCTA | 70392 |
rs234450358 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95509922 | ACCCTCAACTATAAC[A/C]AAATTTTTGATGCTA | 70392 |
rs234451008 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531191 | AAGAAAGCAACCATG[A/G]ATGCCGGGCTTGGTG | 70392 |
rs234452900 | snp | C/G | | | intron-variant | Asb12 | Mm_Celera | X:95521505 | TTCTAAAAAAGAATT[C/G]AATTATGCATCTACT | 70392 |
rs234482974 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500715 | AAGTGTTTGCTTCAG[-/AA]AAAAAAAAATTCTCT | 70392 |
rs234484564 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95529603 | AAATATAAAATGAAT[A/G]CCTATGAAAGCACAA | 70392 |
rs234525450 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95500770 | CCATATGACACAACC[A/G]AGTCTCCAAAGAAAC | 70392 |
rs234533764 | snp | A/G | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501016 | GACAGAAACTAAAGA[A/G]AAATGATGAAACTAA | 70392 |
rs234559075 | snp | A/C | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95501925 | CCAAAACCCTGTACT[A/C]AACAAAACTGGATAA | 70392 |
rs234571838 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95530279 | CTGGGATGAAGCCTA[A/C]TTGATCATGATGGAT | 70392 |
rs234592312 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95492402 | CTGACTCATTAACTG[C/T]GATGGTTCTTCAAAA | 70392 |
rs234601567 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95537184 | ACCATAATAGTGTGG[A/C]TACTTCTATCCATCT | 70392 |
rs234635656 | snp | A/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95510081 | AGTATTGAGAAGGAA[A/T]ACACACATCTCAAGG | 70392 |
rs234688352 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95529362 | AGAAGCCAGATTGAA[A/T]TAGTCACCTTGGAAG | 70392 |
rs234722960 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95500026 | CAAAGCAAACAAAGA[G/T]AATCAAGAAGCAAGC | 70392 |
rs234789500 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95491330 | GAAATACTGTCCCAA[A/C]TATTTATTATTATTA | 70392 |
rs234798231 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95509511 | TAATGCTAAACTAGA[A/T]TATAGAACATGTTGT | 70392 |
rs234814230 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95499259 | TATAAAGAAAGAGAT[A/G]CCTATAAACATACAA | 70392 |
rs234831525 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95477685 | GAAGTTCAAAGCCAG[A/G]CTATGCAGTAGAGTG | 70392 |
rs234844182 | in-del | -/AAAC | | | intron-variant | Asb12 | Mm_Celera | X:95523482 | ACAAAAACAAAAACA[-/AAAC]AAAACAAAACAAAAC | 70392 |
rs234873982 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95537023 | GTAGGCAAATGGATG[A/G]GTCTGGAGTATATCA | 70392 |
rs234971824 | in-del | -/AT | | | intron-variant | Asb12 | Mm_Celera | X:95507738 | CTAGACCCCCTAAAC[-/AT]ATGTAGCAAATGTAC | 70392 |
rs234975073 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95499061 | TGGTGTGGTGAGGAT[A/T]TCCTCTTGGAGACAG | 70392 |
rs234995290 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95549686 | ATGGACTTTTTAAAC[A/C]AGGTTTACTATACCA | 70392 |
rs235007466 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95506652 | CATCAAGACCCAAGT[A/G]TCCCATTCCTGGGCA | 70392 |
rs235049784 | in-del | -/C | | | utr-variant-5-prime | Asb12 | Mm_Celera | X:95554464 | CTGTTTCCAAGTGAG[-/C]CCTGAAGAGCAGAGA | 70392 |
rs235073988 | in-del | -/TAACCCTAGTCAAAGCCACAGCCC | | | intron-variant | Asb12 | Mm_Celera | X:95495723 | TCCTTGCCCTAGAAT[-/TAACCCTAGTCAAAGCCACAGCCC]TAACCCTAGTCAAAG | 70392 |
rs235105427 | in-del | -/TAATAG | | | intron-variant | Asb12 | Mm_Celera | X:95553741 | TAATAATAATAATAA[-/TAATAG]TAATAATAATAATAT | 70392 |
rs235120048 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95517829 | CTCCATGAAAGAGGG[A/G]AAGAAAGGATTTTAA | 70392 |
rs235161833 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507904 | TTTTCCTGATGAGAC[C/T]TGATGTTCCAGGGTG | 70392 |
rs235222557 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95482983 | CCAGTAGAAAAGTTA[A/G]GGGAAGGACTGAAGG | 70392 |
rs235244602 | in-del | -/AC | | | intron-variant | Asb12 | Mm_Celera | X:95522736 | TGGTTTAGAAAGTGA[-/AC]ACACACACACACACA | 70392 |
rs235316768 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95526136 | ATTTTAACTCAACCA[-/TT]TTTTTTTTCTATTAA | 70392 |
rs235328168 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95493818 | CTGAACAACTGGAGC[A/G]AGTGCTGTCCCTGAC | 70392 |
rs235329879 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95485845 | GATGGGCAAGTGCTT[-/A]AAAAAAAAAAAAAAA | 70392 |
rs235362428 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95533831 | AGATATTTATAAAGA[A/G]CAGAGATCCTGGTCC | 70392 |
rs235376729 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95482271 | CACTATTTAGCCACA[G/T]TTGGCCCAGAACCTG | 70392 |
rs235479457 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95526187 | CCCCTCTCTTCCTCC[A/C]TCTCTAACCACCCCT | 70392 |
rs235480414 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95495775 | AGCCACAGCCCTATT[C/T]ACCCTAAAAGATAAC | 70392 |
rs235508436 | in-del | -/CTGCAGCTG | | | intron-variant | Asb12 | Mm_Celera | X:95513717 | AGTAAGCCTGTATCC[-/CTGCAGCTG]CTGACAACAACTCAG | 70392 |
rs235526719 | in-del | -/A | | | intron-variant | Asb12 | Mm_Celera | X:95522081 | CATTTCAATAAAGTT[-/A]AAAAAATATGAGAAC | 70392 |
rs235557412 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95477475 | TTTTGTGGGCGCTAG[A/G]ACATTCCTTCAGACA | 70392 |
rs235587195 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95503840 | ACCAACTGTACATCA[A/G]ACAGAAGGCTAATAT | 70392 |
rs235618237 | snp | C/T | | | intron-variant, upstream-variant-2KB | Asb12 | Mm_Celera | X:95478526 | CTTTCTGTATTTTCC[C/T]TTCTTTAGGGCTCTG | 70392 |
rs235727239 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95532132 | ACATTTGATATGAGG[A/C]TCCCTACACATATAC | 70392 |
rs235815664 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95491678 | TGCTTCCCTGCCCTG[A/G]CATTCCCCTACACTG | 70392 |
rs235850681 | in-del | -/TAG | | | intron-variant | Asb12 | Mm_Celera | X:95502711 | CCTATCTCTTCAATA[-/TAG]TAGTACATGAAGTTC | 70392 |
rs235865924 | snp | G/T | | | intron-variant | Asb12 | Mm_Celera | X:95518231 | GAAAATGTATCAACC[G/T]CAAGTGAGAGAATTA | 70392 |
rs235984910 | in-del | -/TG | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559500 | AAAAAAAAAAAAAAC[-/TG]TGCTTTCTGTCTCTT | 70392 |
rs235988906 | in-del | -/AAAA | | | intron-variant | Asb12 | Mm_Celera | X:95474918 | AACAAACAAACAAAC[-/AAAA]AAAAAAAGAACCCTA | 70392 |
rs236025069 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95500158 | AAGTGTACTTAAATG[C/T]TTTAACCTTCTTCTA | 70392 |
rs236064307 | snp | C/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559063 | GCTACTATACCAAGT[C/G]CTGCTTGACCATTTG | 70392 |
rs236113801 | snp | C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95526839 | CTTTAACTGGATTTA[C/T]AGTACAGGCTAGTAT | 70392 |
rs236115059 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95555793 | CCCCTTCACACTTCC[A/C]GTTTGATTTCTTCAT | 70392 |
rs236142720 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95528718 | AATAAATGATTTTCT[A/G]TCGTCTGGGCCAGTA | 70392 |
rs236154473 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95546120 | CTGCTACATATGCAA[C/T]TGTGGGGTACTGGTT | 70392 |
rs236233632 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95554994 | CCATACTGCATAAAA[C/T]CAATCGTGGTGGTAA | 70392 |
rs236244066 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95484778 | GCAGGTGAGAGTGTG[A/G]ACTATAGAAGCTAAC | 70392 |
rs236260233 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95554778 | ACAAAGGCTCTTATC[A/C]TGACACCTCTATACT | 70392 |
rs236281332 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95528576 | ATAAATAGAAAACCA[A/T]AATCTCTGGCCTACC | 70392 |
rs236320869 | in-del | -/GTGGT | | | intron-variant | Asb12 | Mm_Celera | X:95489954 | GGTTCCCCTGGGGGG[-/GTGGT]GGGGGAAACTCTGAT | 70392 |
rs236356932 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95535601 | GTAGGCAAATGGATG[A/G]ATCTGGAGTATATCA | 70392 |
rs236372134 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95536331 | GGGAGTATGAGCAGG[A/G]GAAGGGGGATAGAAT | 70392 |
rs236392339 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95527782 | TTTCTTGTGTGGGAG[A/T]ATCTACACCTAACCC | 70392 |
rs236393710 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95536270 | GTGAAGGCTCAATGC[C/T]CCAGTGTAAGAGAAT | 70392 |
rs236407189 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95525805 | ATAGACAGACAGGGG[A/G]CTGAAACAGGATGAC | 70392 |
rs236409408 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95514390 | TCAGGGTTGCCTCTA[A/G]CACTGCAGCAGAATA | 70392 |
rs236413598 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95497079 | CAGCATGCTGCCCCT[C/T]CCCCCCTCCCATTGA | 70392 |
rs236502450 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95515638 | TTAGGAAAAAAAAAA[A/C]TCCCCTCGACATGTA | 70392 |
rs236514548 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95524567 | CAAAGCTCTCACACG[C/T]GCTATTGTCTCGCCA | 70392 |
rs236544295 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95497864 | ATAAAAGATAAGACT[A/G]AAGAAAAAAAAGGTT | 70392 |
rs236546009 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95498423 | TTAGTAAGTACCTAC[A/C]ATGTATGTCCTTTTG | 70392 |
rs236586050 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95524794 | CACTCTTGCACATGC[A/G]CACATTGCTTGTTTT | 70392 |
rs236609693 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95498368 | CTTCTTGAGTTTTGT[A/G]GATTGTATCCTGGGT | 70392 |
rs236611860 | snp | A/C/T | | | intron-variant | Asb12 | GRCm38.p3 | X:95487670 | TAAAGCTGGTCTCCA[A/C/T]AGTAATGCTACTTCA | 70392 |
rs236622372 | in-del | -/GAGGAGGAGGAA | | | intron-variant | Asb12 | GRCm38.p3 | X:95531375 | GAGGAGGAGGAGGAG[-/GAGGAGGAGGAA]GAAGAGAAGGAGAAG | 70392 |
rs236680089 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95533005 | TGTGAAGAGTCAGAG[C/T]TTTAGAATGGTTATT | 70392 |
rs236717949 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95507359 | ATTTTTTCTGCCTAT[A/G]AGATATGCATGGATA | 70392 |
rs236731413 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95483372 | TTATCACATATGGTG[A/G]AGTCAAGACATCTCA | 70392 |
rs236761366 | in-del | -/T | | | intron-variant | Asb12 | Mm_Celera | X:95489952 | TGGTTCCCCTGGGGG[-/T]GGTGGTGGGGGAAAC | 70392 |
rs236784763 | in-del | -/TATATA | | | intron-variant | Asb12 | Mm_Celera | X:95553596 | ATGAACATATGTCAT[-/TATATA]TATGTCAATAAGTTT | 70392 |
rs236793598 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95483826 | CTATGTGGGACCATG[A/G]CTACTCACAGCCTTA | 70392 |
rs236841806 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95549499 | TCATTTTGATCAGTC[A/G]TGTGTCTCTGCATTA | 70392 |
rs236856010 | snp | A/T | | | intron-variant | Asb12 | Mm_Celera | X:95494394 | TAGTTGTGTATAAAG[A/T]AGAAACAACAAGAAG | 70392 |
rs236870798 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95550259 | CTAATTGAGGGATAG[A/G]CAAAGTGGTCAGTCA | 70392 |
rs236908541 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95534613 | CTTTTGATAGGAATC[A/G]AATTGAATCTGTAGA | 70392 |
rs236954213 | snp | A/G | | | upstream-variant-2KB | Asb12 | Mm_Celera | X:95559409 | CCAGGCATAGTTACA[A/G]TGGTAATCTCAGGAC | 70392 |
rs236958953 | in-del | -/AAC | | | intron-variant | Asb12 | Mm_Celera | X:95541472 | TAGTAAAAAAAAAAA[-/AAC]CACAAAAAGAAAAAC | 70392 |
rs237046844 | in-del | -/TTTATTTATTTA | | | intron-variant | Asb12 | Mm_Celera | X:95481963 | ATGTTCATCTTGTCT[-/TTTATTTATTTA]TTTATTTATTTATTT | 70392 |
rs237047515 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95508520 | ATATACAATTTAGAA[C/T]GTGAGCCCAATACTA | 70392 |
rs237084034 | in-del | -/TT | | | intron-variant | Asb12 | Mm_Celera | X:95487809 | TTTCTTTTCTTTTTC[-/TT]TTTTTTTTTTTTTTG | 70392 |
rs237117394 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95557640 | AACGCTCAATACCCT[A/G]TTGAACAAGTGATGA | 70392 |
rs237123728 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95517635 | TCAATGAAATGATTC[C/T]TAATGATACTCTGCT | 70392 |
rs237128490 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95531233 | TAATCCCAGCACTTG[A/G]GAGGCAGAGGCAGGC | 70392 |
rs237134327 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95545620 | AAAATTTTTATTAGA[C/T]TAATTGTTATGCATT | 70392 |
rs237145258 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95498008 | GTAATTCCATCTCTC[C/T]ACTTGATGCCCTGTC | 70392 |
rs237194676 | in-del | -/TGGT | | | intron-variant | Asb12 | Mm_Celera | X:95489955 | GTTCCCCTGGGGGGG[-/TGGT]GGGGGAAACTCTGAT | 70392 |
rs237205407 | in-del | -/AA | | | intron-variant | Asb12 | Mm_Celera | X:95490452 | TATAATGCAGTAGTT[-/AA]AAGTTTTAAAAGTAC | 70392 |
rs237211337 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95496968 | TCCTATGCAATACCT[A/C]TTGTGCTGGTTGGCT | 70392 |
rs237212474 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95507768 | ACAGATTGGTCTTCA[C/T]GTGGCGACCCCTAAC | 70392 |
rs237215285 | snp | A/C | | | intron-variant | Asb12 | Mm_Celera | X:95522306 | AAGTGAACTATGGGA[A/C]ATTATCACACAAGCC | 70392 |
rs237242125 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95506149 | ATCTGGACTCCCGAG[A/G]TCTCTCAAACAGTGG | 70392 |
rs237283396 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95517005 | TGACAGGAATGGGAG[A/G]CAGGACATGGGGAGG | 70392 |
rs237332476 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95505252 | TACCCAGATATCCTC[C/T]GACAGAAGAATTGAT | 70392 |
rs237337371 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95506715 | CTTGCTTAACTATGT[C/T]CATAGCAGCTTTATT | 70392 |
rs237359053 | in-del | -/AAAG | | | intron-variant | Asb12 | Mm_Celera | X:95474923 | AACAAACAAACAAAA[-/AAAG]AACCCTAAATCACAG | 70392 |
rs237441610 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95515690 | CAAAATAAAGAGCAT[A/G]TTAAAAGCTGCAAAG | 70392 |
rs237473143 | snp | C/T | | | intron-variant | Asb12 | Mm_Celera | X:95487682 | CCACAGTAATGCTAC[C/T]TCACACAGGTCAGGG | 70392 |
rs237475508 | snp | A/G | | | intron-variant | Asb12 | Mm_Celera | X:95475005 | ACGTAACAGAATGAA[A/G]CTCAATTTCTATCTC | 70392 |