SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27369637 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795473 | GAAGGATGGAGGGTG[A/G]CTGAAACAGCCAGTG | 100504221 |
rs27369638 | snp | G/T | 0.132653 | 0.220748 | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795411 | CCAGGTCATCGTGGA[G/T]AGGACATTCATGTGT | 100504221 |
rs27369639 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795380 | GGCGGATACAGGGTC[C/T]AATTGATCACATGTT | 100504221 |
rs27369640 | snp | C/T | 0.484429 | 0.0868505 | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795348 | CTAGAGGCTTAGCGG[C/T]AGTGGGTAAGTGGGT | 100504221 |
rs27369641 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153793435 | TCATGACCTAGTGTA[A/G]TAAGGGATGACCCAT | 100504221 |
rs27369642 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Efcab8 | Mm_Celera | 2:153792642 | TGACCTACCTCTTCC[A/G]TGGCTCTCAGTTCAT | 100504221 |
rs27369643 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Efcab8 | Mm_Celera | 2:153792495 | ATATATTTTCTTGTG[A/G]CCAGTCGAAGTCCAT | 100504221 |
rs27369644 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Efcab8 | Mm_Celera | 2:153792168 | ATGAAGAGCTGGGTG[C/T]GTAAGGCCTAACATC | 100504221 |
rs27369645 | snp | G/T | 0.32 | 0.24 | intron-variant | Efcab8 | Mm_Celera | 2:153791465 | CTTAAAATCCAGCTC[G/T]CCATTACTGGATCTG | 100504221 |
rs27369646 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153789852 | AGCTGATGACCCACA[A/G]GAGAAGACTGGACAT | 100504221 |
rs27369647 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Efcab8 | Mm_Celera | 2:153789644 | AGCTGGGATTCTCCT[G/T]CGAGGAAGCTACTGG | 100504221 |
rs27369648 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Efcab8 | Mm_Celera | 2:153789095 | GGGCTTGGGACCCTA[A/G]AGGCAAATGTTAAGA | 100504221 |
rs27369649 | snp | C/T | 0.42 | 0.183303 | intron-variant | Efcab8 | Mm_Celera | 2:153783876 | CGTGGAGGGCTCAGA[C/T]CTGGTGCATTTTTAC | 100504221 |
rs27369650 | snp | A/T | 0.375 | 0.216506 | intron-variant | Efcab8 | Mm_Celera | 2:153783875 | GCGTGGAGGGCTCAG[A/T]CCTGGTGCATTTTTA | 100504221 |
rs27369651 | snp | C/T | 0.486111 | 0.0821678 | nc-transcript-variant | Efcab8 | Mm_Celera | 2:153783748 | AGATCAGCAGTTTTC[C/T]GATATGCACCTGGCT | 100504221 |
rs27369652 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Efcab8 | Mm_Celera | 2:153783369 | CAAAAAATGAGCCCA[C/G]GTCCTCTAACATTGC | 100504221 |
rs27369653 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Efcab8 | Mm_Celera | 2:153783192 | ACTCATAAGAGCCCA[A/G]GAATGTTTGCCCCTT | 100504221 |
rs27369654 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153782978 | ATCAGGAAGAATGAA[A/C]AAGAGGAGCATAAGA | 100504221 |
rs27369655 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Efcab8 | Mm_Celera | 2:153782880 | TGAGAGTCTGATTGG[A/G]AAGGAAAGGCAGACT | 100504221 |
rs27369656 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Efcab8 | Mm_Celera | 2:153782844 | CATTTGCCTCCTAGG[A/C]AGATTGCCTGATATA | 100504221 |
rs27369657 | snp | A/G | 0.5 | 0 | intron-variant | Efcab8 | Mm_Celera | 2:153782801 | GAGTAGCCATGAAGT[A/G]TATCAGAGGGAGGCA | 100504221 |
rs27369658 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Efcab8 | Mm_Celera | 2:153782793 | AGTGGAATGAGTAGC[C/T]ATGAAGTATATCAGA | 100504221 |
rs27369659 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Efcab8 | Mm_Celera | 2:153782550 | GCCAAATGTCACACA[A/C]ATGAGCACATCAATT | 100504221 |
rs27369660 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Efcab8 | Mm_Celera | 2:153781974 | AAGTGATAACTTAGA[C/T]GAGCCTAACAAGCAG | 100504221 |
rs27369661 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Efcab8 | Mm_Celera | 2:153781540 | CTGGATTTAAGCTAG[C/T]AATCTTCATGGCTTC | 100504221 |
rs27369662 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780867 | GAGTCCTCAGATTTC[C/T]AGAGATTTGCGTTTT | 100504221 |
rs27369663 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780839 | TTTAAATGTATCTAT[A/G]CCCTAAGCTTATGAG | 100504221 |
rs27369664 | snp | A/G | 0.46875 | 0.121031 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780712 | AGGCCAATACAATTC[A/G]TATAGTTAACAGAAA | 100504221 |
rs27369665 | snp | G/T | 0.297521 | 0.245442 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780093 | CTGGAGGGTAGATGT[G/T]GATGAACAAGGGTGC | 100504221 |
rs27369666 | snp | G/T | 0.18 | 0.24 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780084 | TAGAGTGAGCTGGAG[G/T]GTAGATGTTGATGAA | 100504221 |
rs27369667 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780024 | TTGCATTACGGGCCA[C/T]CTTGGTTTAAGGGAA | 100504221 |
rs27369668 | snp | A/G | 0.345679 | 0.230967 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779932 | TGTTTTTCCTTCAGA[A/G]TTCACAACCATCTGG | 100504221 |
rs27369669 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779659 | GTGACAGATGTTGGC[A/G]AATATTACCCACCAT | 100504221 |
rs27369670 | snp | C/T | 0.486111 | 0.0821678 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779527 | GCTATCAGCCACTTC[C/T]GCCCTACCTTACCTA | 100504221 |
rs27369671 | snp | G/T | 0.142012 | 0.225474 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779407 | AAAGGACTCCAAACC[G/T]TATTTCCGTTCTTCC | 100504221 |
rs27369672 | snp | C/T | 0.493827 | 0.0552116 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779343 | CTTCTGCTCTGTTAT[C/T]CTTCCTTGATTCTCG | 100504221 |
rs27369673 | snp | G/T | 0.165289 | 0.235211 | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779163 | TCTCGCCAACCAGTT[G/T]CCGCTTCGGCCACGT | 100504221 |
rs29554070 | snp | G/T | 0.375 | 0.216506 | intron-variant | Efcab8 | Mm_Celera | 2:153786971 | GCCTTGAACTCGTTG[G/T]GTAGCCCAGGTTGGC | 100504221 |
rs29577206 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153786666 | GGTGCTTGCTGAGAG[A/G]AGCCAGATACTGCAT | 100504221 |
rs29767994 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153786925 | ATTATTGTTAATATT[A/T]TTGAAACAGAGTCTC | 100504221 |
rs33435016 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153785461 | ACGTGTAGGTTCCTG[G/T]GATTGCACTCTTGTC | 100504221 |
rs33447620 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153786535 | GAAGAAAAGCATCCC[A/G]GTAGAAAGAGTGACT | 100504221 |
rs33458894 | snp | C/T | 0.375 | 0.216506 | intron-variant | Efcab8 | Mm_Celera | 2:153786488 | TAGGAAAGTCAAATA[C/T]TGGGGATGGCAGCCT | 100504221 |
rs33521862 | snp | C/T | 0.375 | 0.216506 | nc-transcript-variant | Efcab8 | Mm_Celera | 2:153787701 | GTCGGAAGAGATGCT[C/T]GAGTTGCTGTTCTTG | 100504221 |
rs33593114 | snp | C/T | 0.375 | 0.216506 | intron-variant | Efcab8 | Mm_Celera | 2:153786486 | CATAGGAAAGTCAAA[C/T]ATTGGGGATGGCAGC | 100504221 |
rs33634898 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Efcab8 | Mm_Celera | 2:153786781 | GGTGGCGCCAATTGA[A/C/T]ACCTTTGCAAATAGA | 100504221 |
rs45644233 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153784261 | GGACTTCCTTCTAAG[C/T]TTACATACACTGTCC | 100504221 |
rs45715211 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153789675 | TGGACTCCCTGGCCT[A/G]GCGGCAAGGGCCTTG | 100504221 |
rs45989756 | snp | G/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789900 | GAGTTTTACAGTTTT[G/T]CGAACCTTCCCAGGG | 100504221 |
rs46085396 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153788574 | TCACTGAATTACACT[C/T]GCCTTCCCTCCCTCT | 100504221 |
rs46140678 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789790 | TTCCACTTATGGCCC[C/T]TTTACCCATGGTGTC | 100504221 |
rs46337206 | snp | G/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153790099 | TTTGAGTGCTTGGAT[G/T]ATAGGTGTGTATCAT | 100504221 |
rs46345090 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153782898 | GGAAAGGCAGACTCC[A/G]GTCTTGTGGAGGACT | 100504221 |
rs46347094 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153794488 | GTGAGTGAGTCCCCC[A/G]TGCTCTCCAGGCCTG | 100504221 |
rs46480118 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153791903 | TTAGTTCTAGCTCTG[C/T]TGGGCCTGGGTGAGA | 100504221 |
rs46537288 | snp | C/T | | | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780410 | AACTCACTTTGTAGA[C/T]CAGGCTGGCCTCGAA | 100504221 |
rs46539139 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153791898 | GGGTTTTAGTTCTAG[C/T]TCTGTTGGGCCTGGG | 100504221 |
rs46584358 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153782815 | TATATCAGAGGGAGG[C/T]AAAGTCAGGACCACA | 100504221 |
rs46621381 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153790008 | TGGCTTACTTACTCT[C/T]TGAGAAGACATGTAG | 100504221 |
rs46636343 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153788658 | GGGTGGTCTCGAACT[C/T]TTGGACTCAGGTGAT | 100504221 |
rs46641662 | snp | A/C | | | intron-variant | Efcab8 | Mm_Celera | 2:153794119 | GGGAATGCTCACTGT[A/C]AGGCAAATGGAAGAC | 100504221 |
rs46789134 | snp | C/T | | | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780804 | CCACATCCTGTCTCT[C/T]GTGTTTCCTTTTTCT | 100504221 |
rs46805063 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789434 | AGGTAGGTGGCTTCA[C/T]GGATGAGGGAGCCAA | 100504221 |
rs46830900 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153790188 | GGGCAACGGAGGGAG[A/G]GGTTTGGCACAGAAA | 100504221 |
rs46860957 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153794718 | AAGCCACAGTGCATG[C/T]AAGTCTCTCTAGATT | 100504221 |
rs46886176 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153791772 | GTGGACCTGCAGGGA[A/G]CAATGAGCTGGAGTT | 100504221 |
rs46975167 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789775 | CTGAGCTGCTACTCA[C/T]TCCACTTATGGCCCC | 100504221 |
rs47053794 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153792688 | TTGAATCGTATCTGC[A/G]TGTTTCTCACCATCT | 100504221 |
rs47111476 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153789681 | CCCTGGCCTGGCGGC[A/G]AGGGCCTTGTAAAGC | 100504221 |
rs47165078 | snp | A/C | | | intron-variant | Efcab8 | GRCm38.p3 | 2:153793994 | TGAAGAGACCGAGGA[A/C]GCCTTCCTGGGAAGC | 100504221 |
rs47279788 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789975 | AGGCTTGAGGAAGAG[C/T]GGAAAGTTATGGGAA | 100504221 |
rs47280787 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153794307 | CAGGAAAGATCCCTG[C/T]CCCCTGTACACTCTG | 100504221 |
rs47287756 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153788718 | GACTAAGATGTGTCA[C/T]TATCCCTGGTTCCTG | 100504221 |
rs47335151 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153791753 | TGGGCTCTGCCTTCC[C/T]TCAGTGGACCTGCAG | 100504221 |
rs47339894 | snp | C/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153789605 | AGTTTCATCCCCAGA[C/G]GCACAGGTGGCTCAC | 100504221 |
rs47357834 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153782944 | TGCCATAGGCCAGAG[C/T]TTGGGGTGGGAGATG | 100504221 |
rs47391120 | snp | A/G | | | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795185 | AAAAAATCTGCACAA[A/G]CTAAGGCCCTCTCCC | 100504221 |
rs47428028 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789878 | GACATTTAATGTTAT[C/T]TAATATGAGTTTTAC | 100504221 |
rs47480766 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153794096 | GGTCCATTGGTGAAT[A/G]CCCACTGGGGAATGC | 100504221 |
rs47551302 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153794089 | GCTCCCAGGTCCATT[A/G]GTGAATACCCACTGG | 100504221 |
rs47617571 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153784541 | GAGAAGGGGACCACA[A/G]AGGGTGCGAGCAGCA | 100504221 |
rs47686862 | snp | A/G | | | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780454 | CAGCCTCTGCCTCCC[A/G]AATACTGGGATTAAG | 100504221 |
rs47735567 | snp | A/G | | | nc-transcript-variant | Efcab8 | Mm_Celera | 2:153780921 | TTGCTTCATGCCCTC[A/G]TCCCTCCATGCTCCT | 100504221 |
rs47751593 | snp | C/T | | | nc-transcript-variant | Efcab8 | Mm_Celera | 2:153792798 | CACCAAAGATGGGAT[C/T]CTGCAGTTCTGGTCT | 100504221 |
rs47779854 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153794565 | TGAGCACGCATGGGA[A/G]TCCTCTGGGACTTGT | 100504221 |
rs47834190 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153789487 | GCTTGCCCAGGCTGA[C/T]GGGCAGAAAGAGGCG | 100504221 |
rs47908884 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153791586 | CTTCCCTAAAATGCC[A/G]TTCCCAGGCCCGTGG | 100504221 |
rs47914492 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153792037 | CTTTGCCAACACTGG[A/G]GGCAGGAAAGCAACC | 100504221 |
rs47981228 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153788594 | TCCCTCCCTCTGTCT[C/T]TCCTTTTCCTCTGTC | 100504221 |
rs48169650 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153784442 | AGTGGAGAAACACAC[A/G]AATCACAATCTTATG | 100504221 |
rs48212144 | snp | C/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153782824 | GGGAGGCAAAGTCAG[C/G]ACCACATTTGCCTCC | 100504221 |
rs48248695 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153787981 | GACCGTCTCCTCAAG[C/T]GTTCCCACTGAGGTA | 100504221 |
rs48344945 | snp | C/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153789901 | AGTTTTACAGTTTTT[C/G]GAACCTTCCCAGGGA | 100504221 |
rs48444680 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153791185 | ATTAAATATGAATAA[C/T]GAGAGTTTTCATAAC | 100504221 |
rs48666861 | snp | A/G | | | intron-variant | Efcab8 | Mm_Celera | 2:153792970 | TTAACCCCGGGGGTC[A/G]GGGAGCTCACACTTG | 100504221 |
rs48811745 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153788459 | TTTGGGTATAATCTT[C/T]GTCCACACAACGATT | 100504221 |
rs48815523 | snp | A/G | | | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153780878 | TTTCTAGAGATTTGC[A/G]TTTTATTTCTAGATG | 100504221 |
rs48846828 | snp | A/T | | | downstream-variant-500B | Efcab8 | Mm_Celera | 2:153795534 | GTAGGGCTGTGACTT[A/T]GAGCAGCTATTTACC | 100504221 |
rs48852380 | snp | A/G | | | upstream-variant-2KB | Efcab8 | Mm_Celera | 2:153779593 | TACAGGAAGAAGGAC[A/G]GATTGGGGCCTACCT | 100504221 |
rs48927088 | snp | C/T | | | intron-variant | Efcab8 | Mm_Celera | 2:153790936 | GTGTGGCTGGGGTGT[C/T]GACTCCTGTGTAGTG | 100504221 |