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 |