SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6398007 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:30973452 | GAAAGGACACCCACA[G/T]TTGTAAAAGAAACAC | 65257 |
rs13459123 | snp | C/G | 0.459791 | 0.13597 | missense | Asb3 | Mm_Celera | 11:31058902 | CATACAAAATGTGTG[C/G]AACTTTTGCTGTCCA | 65257 |
rs13460995 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Asb3, Erlec1 | Mm_Celera | 11:30954094 | GAGGAGGTTGTGACG[C/G]GTGGCTGGAGGACGC | 65257 |
rs13460996 | snp | G/T | | | upstream-variant-2KB, missense | Asb3, Erlec1 | Mm_Celera | 11:30954042 | GGCTTGCGGAGCCTG[G/T]TCCCCGGAGGGCCAC | 65257 |
rs13461268 | snp | A/G | 0.46875 | 0.121031 | missense | Asb3 | Mm_Celera | 11:31056121 | ATGCTGAGACTATAA[A/G]ATTGCTTCTTAAACA | 65257 |
rs13461269 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Asb3, Erlec1 | Mm_Celera | 11:30954510 | TCAAACGCAGAGGCC[C/T]GGGACTGACGCCGGT | 65257 |
rs26839711 | snp | C/T | 0.473373 | 0.11227 | downstream-variant-500B | Asb3 | Mm_Celera | 11:31103110 | CAGGAGGTCCATTAC[C/T]TAGGTCTTCATGGGA | 65257 |
rs26839712 | snp | C/T | 0.495868 | 0.0452663 | downstream-variant-500B | Asb3 | Mm_Celera | 11:31103102 | ACTGATACCAGGAGG[C/T]CCATTACTTAGGTCT | 65257 |
rs26839713 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Asb3 | Mm_Celera | 11:31102359 | CTTGCCAGCAACCTG[A/T]GACTGGGTAGATCAG | 65257 |
rs26839714 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime | Asb3 | GRCm38.p3 | 11:31102309 | GTCAATATAGACAGA[A/G]CAGGCTGGTTTCTAA | 65257 |
rs26839715 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Asb3 | GRCm38.p3 | 11:31102062 | CAGAATAAGAGAGCA[G/T]CTTTGTTCCTGTTAG | 65257 |
rs26839716 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | Asb3 | Mm_Celera | 11:31101838 | TGGCAAAAGATACCT[C/G]ATTTTTAGTTTGCAA | 65257 |
rs26839717 | snp | G/T | 0.497041 | 0.0383476 | utr-variant-3-prime, downstream-variant-500B | Asb3 | GRCm38.p3 | 11:31101673 | TATAATCTGTTCTCA[G/T]TCCTTAATTCAAACA | 65257 |
rs26839718 | snp | C/T | 0.345679 | 0.230967 | synonymous-codon | Asb3 | Mm_Celera | 11:31101230 | GGATGGAGAAACCAG[C/T]AAGGCCACCTGACAC | 65257 |
rs26839719 | snp | A/T | 0.497778 | 0.0332592 | synonymous-codon | Asb3 | Mm_Celera | 11:31101041 | TGTTTCTCCAGCCTC[A/T]GTTCCAAGCCTAACC | 65257 |
rs26839720 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31100645 | ATGTAGTCATGCTGA[A/C]CCAGTAGTCTTCTTT | 65257 |
rs26839721 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Asb3 | Mm_Celera | 11:31100611 | GATCAAGCAAGTGGA[A/C]AAAGTACATACACGT | 65257 |
rs26839722 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Asb3 | Mm_Celera | 11:31100602 | TTGAAGTGAGATCAA[C/G]CAAGTGGAAAAAGTA | 65257 |
rs26839723 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Asb3 | Mm_Celera | 11:31100451 | ACGTTCAGAACCTTT[A/G]GTAGTAAAACAGACT | 65257 |
rs26839724 | snp | A/C | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31100429 | ACATCCCTCGGTTTC[A/C]TGTGTTACGTTCAGA | 65257 |
rs26839725 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Asb3 | Mm_Celera | 11:31100071 | ATACAAAACTAGAAT[A/G]TGTGGTGGGTGTGTA | 65257 |
rs26839726 | snp | C/G | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31094454 | TGTTGGGATCAAATG[C/G]ATCTGAATGGCTCTG | 65257 |
rs26839727 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31094433 | ATACTCATCAACGCT[A/T]AGAGGTGTTGGGATC | 65257 |
rs26839728 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31094412 | ATCCTCCGGTGGCTA[C/T]ATCAGATACTCATCA | 65257 |
rs26839729 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Asb3 | Mm_Celera | 11:31094254 | TCTTTACTAACAAAA[A/T]ATCGAGTCACATAAA | 65257 |
rs26839730 | snp | A/G | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31094225 | ATGCTCCATCTCACA[A/G]GGATTTCGAGATTTC | 65257 |
rs26839731 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Asb3 | Mm_Celera | 11:31094180 | CTCCATGGTACTTGA[G/T]TTGATGCTCCTGCCC | 65257 |
rs26839732 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Asb3 | Mm_Celera | 11:31093955 | TAGTCTACTTTGTTT[A/C]AGGTTACTTTCCATT | 65257 |
rs26839733 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Asb3 | Mm_Celera | 11:31093715 | TTTGTTTTCAAAACC[C/G]TCACTATTCTTATCT | 65257 |
rs26839734 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Asb3 | Mm_Celera | 11:31093302 | AGATCCAAATGATGA[C/T]CTCCAAGTGCATACA | 65257 |
rs26839735 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31093264 | TTGCCTACCACATTG[A/C]AGCAATATAACTGTT | 65257 |
rs26839736 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb3 | Mm_Celera | 11:31093254 | CTTAAATGATTTGCC[C/T]ACCACATTGCAGCAA | 65257 |
rs26839737 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Asb3 | Mm_Celera | 11:31093117 | TTAAAGTTTCTTTAA[A/G]TGTCAACAGCCTTAT | 65257 |
rs26839738 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31093056 | AGGGAATTTAGCTGC[C/T]TTTGAACACCCAAAT | 65257 |
rs26839739 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Asb3 | GRCm38.p3 | 11:31093034 | GTAATTTGATCAAAA[A/G]ACTTCCAGGGAATTT | 65257 |
rs26839740 | snp | A/G/T | 0.497041 | 0.0383476 | intron-variant | Asb3 | GRCm38.p3 | 11:31092799 | CCCTTCAGTGTTGAT[A/G/T]TGAAAATTACCTTCT | 65257 |
rs26839741 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Asb3 | Mm_Celera | 11:31092455 | GCTCTGATTATAACC[A/G]TTTAGTTGTTCAAGT | 65257 |
rs26839742 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Asb3 | Mm_Celera | 11:31092222 | TCCTTATTGAACCTG[C/T]TGAAATATTTAAGTT | 65257 |
rs26839743 | snp | G/T | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31091297 | TCTCTGGAATCTTTT[G/T]GAGGGTGTACAGGTA | 65257 |
rs26839744 | snp | A/C | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31090985 | TTCCATCAAGGAGAT[A/C]AAATTTCAGTTAAAC | 65257 |
rs26839745 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31089218 | AATTGAATACTCCAG[A/G]ACAGCTCACTCCACA | 65257 |
rs26839746 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Asb3 | Mm_Celera | 11:31088924 | ATTCTGTTCTAACAA[A/G]TCATAGTTGGCCAGT | 65257 |
rs26839747 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Asb3 | GRCm38.p3 | 11:31088849 | TGGAGGAACCTCTGC[A/G]CTGTCTTGCACCGTC | 65257 |
rs26839748 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Asb3 | Mm_Celera | 11:31088768 | GTTGGGTAATTTTCC[C/G]GGGATTCTCCATCAA | 65257 |
rs26839749 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31087487 | GCTTCTTGTTCTTTT[C/T]TCTAGCTACAACCTC | 65257 |
rs26839750 | snp | C/G | 0.495 | 0.0497494 | intron-variant | Asb3 | Mm_Celera | 11:31087287 | GAACAGATAGAATGT[C/G]GGAGAGCGAATTTGA | 65257 |
rs26839751 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Asb3 | Mm_Celera | 11:31087138 | GAAGTTTTCTATTTG[A/G]AGTCTCCTGGCGTTC | 65257 |
rs26839752 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31085675 | GTACAAATCTTACAG[A/G]GAGCAGCAATTGACT | 65257 |
rs26839753 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Asb3 | Mm_Celera | 11:31084655 | GGGATAGCCAGACTA[C/T]ATTTGGCAAAACAGC | 65257 |
rs26839754 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Asb3 | GRCm38.p3 | 11:31084521 | AGCTGCATAACTTCT[A/T]GGAATAGTTAAGGAG | 65257 |
rs26839755 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31084363 | CCTCTTTTAGTTGGA[C/T]TGATAGGGAATCCTG | 65257 |
rs26839756 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Asb3 | Mm_Celera | 11:31083473 | TCTGAGGAACCAACA[A/G]CTAAACTGCCCTTTC | 65257 |
rs26839757 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31083298 | TGGTACATACTCCAT[G/T]TCTAAGATTTGTTAG | 65257 |
rs26839758 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31083104 | ATCCTTTGTTCTCTA[A/C]CCAACTAAGTCAACT | 65257 |
rs26839759 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Asb3 | Mm_Celera | 11:31082737 | TAGCGATGCCTGTCT[C/T]CAGAGCATGCACTTT | 65257 |
rs26839760 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Asb3 | Mm_Celera | 11:31082694 | TAGCTATAGACAGTT[C/T]GACAGTCTGTTCTCC | 65257 |
rs26839761 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Asb3 | Mm_Celera | 11:31082064 | TAGAACCAAAGCCTC[C/G]GGTCTAATAGAGAAG | 65257 |
rs26839762 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31081928 | TATGAATGTTGAGTC[A/G]GGATTCTGTGGTGAC | 65257 |
rs26839763 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Asb3 | Mm_Celera | 11:31081143 | CAATGCAGAGCGATT[A/G]ATACAAAAAGTTTTC | 65257 |
rs26839764 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Asb3 | Mm_Celera | 11:31080148 | TTGTTTTTCCATGTA[A/G]CTATCTGCACTGGCT | 65257 |
rs26839765 | snp | A/G | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31070746 | TTTGGTTGAAATAGG[A/G]TCTCACGAGAACCTC | 65257 |
rs26839766 | snp | G/T | 0.375 | 0.216506 | intron-variant | Asb3 | Mm_Celera | 11:31070671 | TAACTGTCCAGTGAC[G/T]TTTTCATCTTCTTTT | 65257 |
rs26839767 | snp | C/T | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31070334 | AATTTCTGCTACAGA[C/T]AATACTGTTAATAAT | 65257 |
rs26839768 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Asb3 | Mm_Celera | 11:31070249 | CATGTAACTGTCAAA[C/G]TTGAAGTTTTGATGA | 65257 |
rs26839769 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Asb3 | Mm_Celera | 11:31070117 | CAGCCCACAGAATGC[C/G]AATTTCAAAGGGATT | 65257 |
rs26839770 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Asb3 | Mm_Celera | 11:31070078 | GTTTTCCATCACTCT[A/G]CCACCTACTTGCTGG | 65257 |
rs26839771 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Asb3 | Mm_Celera | 11:31069787 | GTTGGTTTTGGGTCT[C/T]CTCTCTGCAGGTCCT | 65257 |
rs26839772 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb3 | GRCm38.p3 | 11:31069643 | GTTTGTCCAAAGCTA[A/T]GATTCCAAAGGAAAT | 65257 |
rs26839773 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31061710 | TGCTGCAGTATCTGT[C/T]GTTCAGTTTAGCAGA | 65257 |
rs26839774 | snp | A/G | 0.231111 | 0.249285 | missense | Asb3 | GRCm38.p3 | 11:31061436 | GGGCTTGTGACACTG[A/G]ACCAGACAAAGTGAG | 65257 |
rs26839775 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Asb3 | Mm_Celera | 11:31061298 | TGCGCCACCACTATC[G/T]TCTAGTCAGTGGATG | 65257 |
rs26839776 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Asb3 | Mm_Celera | 11:31060182 | ATAGGAATTTGGTCT[A/T]ATGTTCAATTTCAAG | 65257 |
rs26839777 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Asb3 | Mm_Celera | 11:31060138 | TTTAAACAGTTGTAC[C/T]CAGTTTTAAATTAAT | 65257 |
rs26839778 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb3 | Mm_Celera | 11:31060065 | CCCCCTTTTCACTCA[A/G]TTTGTGTCCTTTACA | 65257 |
rs26839779 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Asb3 | Mm_Celera | 11:31059891 | TAAAACTCAGACATG[C/T]TTATTTACAAGTTGT | 65257 |
rs26839780 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Asb3 | GRCm38.p3 | 11:31059654 | AAATCAGTATGGACA[A/G]GTTTCAAAATCATGT | 65257 |
rs26839781 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Asb3 | Mm_Celera | 11:31059375 | AATTTGCATTATCTC[C/T]GTGTTTGCAAAAAGA | 65257 |
rs26839782 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Asb3 | Mm_Celera | 11:31059190 | TATTTTTTGGTCTGG[C/T]CCTCTACATCTTTGA | 65257 |
rs26839783 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Asb3 | Mm_Celera | 11:31059090 | ACCTCCAGGTAAAAT[G/T]CTTGGTCATTCCTTT | 65257 |
rs26839784 | snp | A/G | 0.35503 | 0.226867 | synonymous-codon | Asb3 | Mm_Celera | 11:31058925 | GCTGTCCAGTGGGGC[A/G]GATCCTGACCTTTAT | 65257 |
rs26839785 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Asb3 | Mm_Celera | 11:31058088 | TGTGATATTCTTTTC[A/T]CAGACTTCCAAGGGC | 65257 |
rs26839786 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb3 | Mm_Celera | 11:31057887 | CATGTATATCAGTCA[C/T]TTATTGGTAATGTTT | 65257 |
rs26839787 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Asb3 | Mm_Celera | 11:31057451 | TTGACACAATCATGT[G/T]TTAGTGTGAGACCTA | 65257 |
rs26839788 | snp | C/T | 0.375 | 0.216506 | intron-variant | Asb3 | Mm_Celera | 11:31057129 | ACTAGAAGTTTGGCT[C/T]TTTTTTTATTTATTT | 65257 |
rs26839789 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb3 | Mm_Celera | 11:31056266 | CCTTTGTGCTCTCAT[A/G]CTTTTTAACTGTGTT | 65257 |
rs26839791 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Asb3 | Mm_Celera | 11:31055971 | TAGAGTAATTTGATG[C/T]CATATATTTTTCATC | 65257 |
rs26839792 | snp | G/T | 0.5 | 0 | intron-variant | Asb3 | Mm_Celera | 11:31055635 | CCTTTTCTATACCGT[G/T]TTTTGCTTTCTGTTT | 65257 |
rs26839793 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Asb3 | Mm_Celera | 11:31055410 | GAAGTGTCCAGCTTT[A/C]CAAACATCTTTTTGG | 65257 |
rs26839794 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Asb3 | Mm_Celera | 11:31055305 | TACAAGTAAAACTGG[A/G]TTAAGATAGTTGACA | 65257 |
rs26839795 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Asb3 | Mm_Celera | 11:31055286 | ACATGGAGGCCTACA[A/C]ATATACAAGTAAAAC | 65257 |
rs26839796 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Asb3 | Mm_Celera | 11:31048578 | TTGTGGTTATTATTG[C/T]AGTCAGTTCAACTAC | 65257 |
rs26839797 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Asb3 | Mm_Celera | 11:31048466 | AAGCAGTTTACAGAT[C/T]GACAGCAGTTAATGA | 65257 |
rs26839798 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Asb3 | Mm_Celera | 11:31042501 | TGATAGTTAAGAAGA[G/T]TAAATGGAAGTGTTT | 65257 |
rs26839799 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Asb3 | GRCm38.p3 | 11:31042463 | CATTTTCATTTCTGG[G/T]TTTTGAATTAAATGC | 65257 |
rs26839800 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Asb3 | Mm_Celera | 11:31042403 | AAAACATTTAACACT[A/G]GGATCCTACTTTTGC | 65257 |
rs26839801 | snp | G/T | 0.42 | 0.183303 | intron-variant | Asb3 | Mm_Celera | 11:31028828 | CCTGTTTCATTCAAC[G/T]TCACATATAGTCTTT | 65257 |
rs26839802 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Asb3 | Mm_Celera | 11:31022835 | GCTAGTTTGGCATGA[A/G]TGGTTTCAAGAGGGT | 65257 |
rs26839809 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Asb3 | Mm_Celera | 11:31018204 | CTTTCCTTTGAAGGC[A/G]CTTTCTTCTTTGTGC | 65257 |
rs26839810 | snp | A/C | 0.5 | 0 | intron-variant | Asb3 | GRCm38.p3 | 11:31017926 | TGCTATCAAGTCTGA[A/C]TCCCTGACTCCCACA | 65257 |
rs26839811 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb3 | Mm_Celera | 11:31003860 | TGACCAGGTGAATAT[C/T]GTAATCTGTCCAGGT | 65257 |