SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31068404 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435703 | TCTTCAGAATTCTGG[A/C]AAATATTGAAGACCA | 68854 |
rs31087083 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb11 | Mm_Celera | X:164450310 | TGTTTAGAATTCCAT[A/G]GTAATGGTTTCTACT | 68854 |
rs31203300 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435685 | TGCTGTCATTAGAGC[A/C]TGTCTTCAGAATTCT | 68854 |
rs31214488 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Asb11 | Mm_Celera | X:164459208 | ATATATATATATATA[C/T]ATATATATATATATA | 68854 |
rs31216891 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436071 | ATGGGCTCTGCTAAC[C/T]TTCCCTGCAAGCTAG | 68854 |
rs31252090 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | GRCm38.p3 | X:164457791 | AATCTGCTTTTTTTT[C/T]CCATTTTTTTTATAC | 68854 |
rs31331028 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435418 | TTTATGGGTTGTCAG[C/T]GCAACTATATCTGAA | 68854 |
rs31374326 | snp | C/G | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164437535 | GCATTACTTCTCTTT[C/G]ATATTTTCAGTCCAT | 68854 |
rs31449575 | snp | A/C/G | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435908 | AATACACTTGGACTT[A/C/G]CAGCAGATTTTACAT | 68854 |
rs31449578 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435936 | CATATGTGGAGAAGC[C/T]ACATACAAACAAGAA | 68854 |
rs31449581 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436013 | TTACTTGTATTGGCC[A/G]GCTGATAAGAGGACA | 68854 |
rs31450554 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436037 | GAGGACACTGCCCAG[A/C]TAAGGAAGAGACGGA | 68854 |
rs31450557 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436184 | GCCTCAAACAGGAAA[C/T]GAATGCTGAGGGGCC | 68854 |
rs31450560 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436250 | ATCACCTCAGCACTT[C/G]AGTCACATTCAAACT | 68854 |
rs31450563 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436623 | AGTCCTCTATGCATA[C/T]ATCTGATAGGTTTTA | 68854 |
rs31451324 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164440208 | AATTTATTCAAAGAA[C/T]CTGAGAACCAGAGAT | 68854 |
rs31451327 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164440553 | GAACAGGAATAAAAA[C/G]CAGGGGACCTTCCCT | 68854 |
rs31451330 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164441334 | GGCAGTTGCCTGAGT[A/G]AATTGTCCTGCTGTG | 68854 |
rs31451333 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164441384 | AGAAGGAGCAGCAGA[A/G]GAGAGACGAAGTGAG | 68854 |
rs31451396 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436638 | CATCTGATAGGTTTT[A/G]TTGCAATCCAATGTA | 68854 |
rs31451399 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436891 | TTGTCATAAATGTCA[A/G]CACACCCAGTCACCA | 68854 |
rs31451402 | snp | G/T | 0.142012 | 0.225474 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164436933 | GATTAGACAGAGTTC[G/T]TGGTAACAGGAGCAC | 68854 |
rs31452156 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164441612 | GGTGCAGGATCCACA[C/T]GCCCAGAGGAAAAAT | 68854 |
rs31452159 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Asb11 | Mm_Celera | X:164441701 | ATGACCAGGGACTTC[C/T]AACTTGAAGGTGCTG | 68854 |
rs31452162 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-5-prime | Asb11 | Mm_Celera | X:164442171 | TGCAGAGAAGTACAC[A/G]AGGGCTTAGGGAACA | 68854 |
rs31452415 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164437233 | ACTGTCAGGTAAAAA[A/C]GATTTGAATTTCTTC | 68854 |
rs31452417 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb11 | Mm_Celera | X:164437484 | GTTTTAAAGGCTATC[C/T]TGAGAGACTTCCTAC | 68854 |
rs31452420 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164437510 | CCTACTAACCCAGAG[C/T]CCTCATAGAGCATTA | 68854 |
rs31452686 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164449084 | ACAGCTGGGTATCCA[A/C]AAGTCTTACATATGA | 68854 |
rs31452689 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb11 | Mm_Celera | X:164449555 | CCTGTTTTCTTTTCT[A/G]TTATCACTGAATAGC | 68854 |
rs31452691 | snp | A/C | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164449661 | TTTCTTTTCTTATTA[A/C]CACCTTCCACCACAG | 68854 |
rs31452955 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164442864 | GCATGGTGGTGGTGT[A/G]TCAGCACTCCGAAAG | 68854 |
rs31452958 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb11 | Mm_Celera | X:164442950 | GTAGTTCCTCAGGCT[C/T]CGGGGGTTGACTAAC | 68854 |
rs31452961 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb11 | Mm_Celera | X:164443027 | TGCTTCCGTGGCTCC[A/G]GCTGCTGAGCTGCTA | 68854 |
rs31453455 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164437632 | TTGAGAAGCACTGTG[C/T]CATGCTGTATGTATG | 68854 |
rs31453458 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164437719 | AAGTCACTAGACCCA[C/T]TTATACATCAGTGGC | 68854 |
rs31453461 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164437735 | TTATACATCAGTGGC[A/G]CCACAGACAGCAGTA | 68854 |
rs31453566 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164450390 | AGAAACCTGTTGAGC[A/G]GCATTGCTTGATTTG | 68854 |
rs31453569 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb11 | Mm_Celera | X:164450857 | TCAACCAACATTTTG[C/T]ACATTGTCAAAGTAA | 68854 |
rs31453572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164451595 | GTTCCCAGATTGTTA[C/T]CAATTCTATTCTATG | 68854 |
rs31453694 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164443060 | GTGCGTAAGGACTGG[C/T]TTCAAATCTTCCAGT | 68854 |
rs31453697 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb11 | Mm_Celera | X:164443150 | ATGAGAGGGAGACTA[A/G]AGATCATATGCAAAG | 68854 |
rs31453700 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164443382 | TGGTGGCTTGCCAAG[C/G]AAGGTCCACAAGATG | 68854 |
rs31453703 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164443513 | ATTCTGTTTCACTGG[C/T]ATGGAGGGAGTACGT | 68854 |
rs31453725 | snp | C/T | 0.5 | 0 | intron-variant | Asb11 | Mm_Celera | X:164456577 | CTGACCAAATAATGA[C/T]GTGGTTTGCTTCTTC | 68854 |
rs31453728 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | GRCm38.p3 | X:164456752 | TTGCACATCCATACA[C/T]TGAGAGAACATTTTC | 68854 |
rs31453731 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | GRCm38.p3 | X:164456894 | TTGAACTCTTAAAAG[C/T]GCTTAGAACTTTACA | 68854 |
rs31454194 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164437853 | AGTCTACATCCCTTT[A/G]TGCTAGAATTGCCCC | 68854 |
rs31454197 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164437917 | GAGGATTCTAAAATT[A/G]TTCAAAGTTGCTCCA | 68854 |
rs31454200 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Asb11 | Mm_Celera | X:164438046 | TTCCTGATTTCAATG[C/T]ACTAGACAACTCGGA | 68854 |
rs31454203 | snp | A/C | 0.124444 | 0.216185 | intron-variant, missense | Asb11 | Mm_Celera | X:164438133 | AACAGAAAATGCTTC[A/C]ACTAGCTGGTGAAGA | 68854 |
rs31454526 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164443842 | CAGAAATCAGTGGAG[A/G]TATATAAAAAGCACA | 68854 |
rs31454529 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164443972 | TATCTATTTATTTTT[C/G]TCTTGGTTCAAAGTT | 68854 |
rs31454532 | snp | G/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164444044 | TACAAGGAATTCCCA[G/T]TCCTCTGCCAAAGCC | 68854 |
rs31454544 | snp | A/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164451668 | TAAGTATTAGTAATA[A/T]TTTTTTACATCTAAA | 68854 |
rs31454547 | snp | A/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164451700 | GCACGTTGAGTTTCT[A/T]TGTGTAGACCTGAAT | 68854 |
rs31454549 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Asb11 | Mm_Celera | X:164451870 | TCAAAGTCTGTGCTT[G/T]GAGTCACAAGCTGAT | 68854 |
rs31454552 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164452050 | GAGCAATGGAGGAAC[A/G]GAAGAAAATGGGCCA | 68854 |
rs31454684 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164457054 | TCCAAGCTCCAAGAC[C/T]TGAATCCAAATCTCC | 68854 |
rs31454687 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164457290 | TCTTTAGCTTGCTCT[C/T]ACACTTTAATTAGCA | 68854 |
rs31454690 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164457380 | GCCAGTTTGGAAAGT[C/T]CTTTTTTCAATTGTT | 68854 |
rs31454693 | snp | G/T | 0.5 | 0 | intron-variant | Asb11 | Mm_Celera | X:164457387 | TGGAAAGTTCTTTTT[G/T]CAATTGTTAGCTGAG | 68854 |
rs31455036 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164438432 | TGTAGTTGTTCCTGT[A/G]CGTGACTCCTGTCTT | 68854 |
rs31455039 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | GRCm38.p3 | X:164438501 | AGAACCTGGGTAATC[A/C/T]TGCTTTGGATTTGAA | 68854 |
rs31455042 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164438713 | TATATGTTTGCCTAT[A/G]TATATGTGTGTTCTC | 68854 |
rs31455255 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Asb11 | Mm_Celera | X:164444184 | GAGTCTCCATCTCCC[A/T]TGCCACTGGCTCCAG | 68854 |
rs31455258 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164445235 | TGCTTTTGGGGATCA[C/T]GCCATCTGAAAAGGG | 68854 |
rs31455261 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Asb11 | Mm_Celera | X:164445406 | CCAGTCCTCTTTTCT[A/G]TATCTCTTCAGATTT | 68854 |
rs31455485 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164452123 | TTTGAAATGTGTGTG[C/T]CATATCCTTCCTTCT | 68854 |
rs31455488 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164452144 | CCTTCCTTCTACACC[A/G]GCTTATTAGTATTTT | 68854 |
rs31455491 | snp | C/G | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164452854 | ATATGCACTTGGTGA[C/G]AAGGAGTGAGTAAAT | 68854 |
rs31455606 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164457597 | TAGGTTCTAGCTTAG[C/T]TGCTTCATTTCTGGT | 68854 |
rs31455609 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb11 | Mm_Celera | X:164457617 | TCATTTCTGGTTGTA[C/T]GTCTTGTTCCAGATT | 68854 |
rs31455612 | snp | C/T | 0.5 | 0 | intron-variant | Asb11 | Mm_Celera | X:164457671 | CTGCCATTCTCAATT[C/T]CCAGCATTTTAACTA | 68854 |
rs31455955 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164438893 | GGCAGCAGCAACATT[C/T]TGTGAGCCAGAAGTA | 68854 |
rs31455958 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164439181 | TAGTGAATTGACTTA[A/G]AAACTCTCTCATCTC | 68854 |
rs31455961 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Asb11 | Mm_Celera | X:164439267 | CACAAATAGAAAGGA[A/G]AAATTGCTTAACCTG | 68854 |
rs31456114 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164445469 | TATGAATGGAGACGA[C/T]GTGAGTTACTGGAAA | 68854 |
rs31456117 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164445621 | CCACTGTGCTCTGTT[C/T]CCTGTATTTGATAAG | 68854 |
rs31456120 | snp | A/C | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164445903 | GCTCAGGGCCAGCAC[A/C]GCCATTTCCGCATCT | 68854 |
rs31456123 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb11 | Mm_Celera | X:164447026 | TGTTTTGGACTCTGC[A/G]TGTGAGCGGCGGAAA | 68854 |
rs31456354 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Asb11 | Mm_Celera | X:164453033 | GGCTTCACCGATCCA[C/T]GAAGCAGTGAAGCGA | 68854 |
rs31456357 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453075 | CACTCCGGGACATGC[A/G]GAATATCGATGGGCT | 68854 |
rs31456360 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453149 | TAGTCTAGATGTTTT[C/T]ACCTACAGGCATCTG | 68854 |
rs31456363 | snp | A/G | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453319 | AATAACAGCTTGTGC[A/G]AGCATGCGTGAGTCA | 68854 |
rs31456495 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Asb11 | Mm_Celera | X:164457848 | GAGGGTTTGTATAAG[C/T]CAGTAGGTAATTGCT | 68854 |
rs31456498 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164458045 | GGGGGCTCTTTCAGG[A/C/T]ATGAGGAGGAAGCCA | 68854 |
rs31456501 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Asb11 | Mm_Celera | X:164458176 | GGCAGCGCTTCCTGC[A/C/T]CACACCTTCTCTGTA | 68854 |
rs31456536 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435160 | CAGAGGGATTTTTTT[A/T]AATATGTTTATATTC | 68854 |
rs31456539 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Asb11 | Mm_Celera | X:164435288 | CATTCCTGTGTCTAC[A/G]GCACCGAACAAAGTG | 68854 |
rs31456864 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164439366 | AGATACGAGCTTGTG[A/G]GATAATAGAATCTTC | 68854 |
rs31456867 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164439433 | AAGGCTAAAACCTTA[A/G]TTCATTTTCCAAGTT | 68854 |
rs31456870 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164439514 | AGTATTCTTGCCTTT[G/T]ATCGGGTTTTCGTCC | 68854 |
rs31456873 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164439632 | ATCTCAGGTGCCAAG[C/T]AAGGACAACGAGTTC | 68854 |
rs31456956 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb11 | Mm_Celera | X:164447036 | TCTGCATGTGAGCGG[C/T]GGAAATGAGTCACTG | 68854 |
rs31456959 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb11 | Mm_Celera | X:164447068 | TTTCTTTCCCATGTT[C/T]TCTCTATCACCTTGC | 68854 |
rs31456962 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb11 | Mm_Celera | X:164447116 | CTCCTTTGGATTTAA[A/G]CAGTGGGGATAGTGA | 68854 |
rs31457246 | snp | A/C | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453624 | ACTGATATACTTAAA[A/C]TTGCCCATGTTGATC | 68854 |
rs31457249 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453675 | CACAGAGAATGCCTG[A/C/T]TTATGGAGTTCTGCA | 68854 |
rs31457252 | snp | C/G | 0.375 | 0.216506 | intron-variant | Asb11 | Mm_Celera | X:164453688 | TGCTTATGGAGTTCT[C/G]CATCGCTAGTGAATT | 68854 |