SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13476391 | snp | C/T | 0.472318 | 0.114344 | intron-variant | Nacc2 | Mm_Celera | 2:26095521 | GCAGATGGAAAATGC[C/T]GGAGCACACAGCATG | 67991 |
rs27201617 | snp | C/T | 0.5 | 0 | intron-variant | Nacc2 | Mm_Celera | 2:26119678 | TTCATCACCTGATTA[C/T]ACTCAGGCAAAGCAG | 67991 |
rs27201618 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Nacc2 | Mm_Celera | 2:26118289 | TCTCTCCAAATTGGG[C/T]TGTGAGTAAGAAGAG | 67991 |
rs27201619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26118003 | AACTTAACAAAGGCG[C/T]TTAGCAGCACAATAG | 67991 |
rs27201620 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26116319 | AAATGTGCCTTTCTG[C/G]TGTTTAAAGTCAGGG | 67991 |
rs27201621 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nacc2 | Mm_Celera | 2:26115875 | CAGAGAAACCGAGGC[A/C]CTGGATCAGGACCCA | 67991 |
rs27201622 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26114705 | AGGAGGGACAGAGGT[A/C]TATCTCCAAACCCTG | 67991 |
rs27201623 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nacc2 | Mm_Celera | 2:26112878 | AGCCACACATTCCTC[G/T]ACCAAGGCCAGCCTG | 67991 |
rs27201624 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26110230 | CTGGCTCAGGCATCA[A/G]CAGTGCATGGAAGGG | 67991 |
rs27201625 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26110216 | TACCCAGAAGGCACC[C/T]GGCTCAGGCATCAAC | 67991 |
rs27201626 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26110184 | ACCCAGTGTCATAGC[A/G]GAAACTAAGCTCTAT | 67991 |
rs27201627 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26110161 | TGCTAGCCTTCATGT[A/G]TCACCAAACCCAGTG | 67991 |
rs27201628 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26110090 | GAAGGGTGAAGGCTG[C/T]CTGTAGGTTAGCCAC | 67991 |
rs27201629 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nacc2 | Mm_Celera | 2:26110056 | ACACTTGAAGCCTTC[A/G]GGAAGCCCTGGACCC | 67991 |
rs27201630 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Nacc2 | Mm_Celera | 2:26109814 | CCCTTGAGGCCAGTT[A/T]AAAACTCTCCACCCG | 67991 |
rs27201631 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26109773 | AGAAAATGATCCCTG[A/G]AGGAGGAATCCCTGA | 67991 |
rs27201632 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26109569 | GCCACCTTAGAGCTG[A/G]CCAGTTAGACCTGGC | 67991 |
rs27201633 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26109349 | CTCTAAAGGCATCCA[A/G]AATCCAATCTAGGTT | 67991 |
rs27201634 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26109334 | CACCTGGGTTGCCCC[C/T]TCTAAAGGCATCCAG | 67991 |
rs27201635 | snp | A/C | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26108843 | AGCCTGGAAATGGCT[A/C]ATGGCTACACCAGTG | 67991 |
rs27201636 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26108810 | CCAGCTCACGTTGGA[A/T]GTCAATGTGTTCAGC | 67991 |
rs27201637 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26108630 | TTAAAGGCGGGACTC[C/T]TGGCCAACCTCTCCT | 67991 |
rs27201638 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Nacc2 | Mm_Celera | 2:26108615 | CTGTCATAGTACAGT[C/T]TAAAGGCGGGACTCC | 67991 |
rs27201639 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26108567 | CTGCAGGCAACAGCC[A/G]GACACCTAGCTCCCA | 67991 |
rs27201640 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26108550 | AGGTTCCTGGAAGTC[A/C]TCTGCAGGCAACAGC | 67991 |
rs27201641 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26108471 | CATCCTGGATTCCAA[A/G]CAAGGGAGCACAAGG | 67991 |
rs27201642 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26108372 | GGATGCTTGCCCAAA[A/G]TGCCACAGACGGCAG | 67991 |
rs27201643 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26108220 | TCAGATCCTAAAAAC[C/T]ACTGAGACACATGTG | 67991 |
rs27201644 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26108039 | TCAGGCACCTGTCCC[C/T]TGGGAGCTAACATCC | 67991 |
rs27201645 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26106360 | CTACAGTGAACTGAC[A/G]CTGACAGAGTTCAGA | 67991 |
rs27201646 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26106348 | AAAGAGCCCTGACTA[C/T]AGTGAACTGACGCTG | 67991 |
rs27201647 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26106165 | CTCCAAACCCAGCTC[A/G]CAGCGCCTGTGAAGG | 67991 |
rs27201648 | snp | C/T | 0.5 | 0 | intron-variant | Nacc2 | Mm_Celera | 2:26105984 | GTTGAACCCAGGTCA[C/T]ACCCTGACTCCCATC | 67991 |
rs27201649 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26105956 | ACCTAGTCTTTTTTG[C/T]TCTCATACTGGAGTT | 67991 |
rs27201650 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nacc2 | Mm_Celera | 2:26105791 | AATACAAAACACACA[C/T]GCTCTCTTTCTCATA | 67991 |
rs27201651 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26105702 | AGTAGAGTCCCACAT[C/T]TCTTCTGAATACAGA | 67991 |
rs27201652 | snp | A/C/G | 0.401235 | 0.199068 | intron-variant | Nacc2 | GRCm38.p3 | 2:26105054 | TACTCAGCCATGTAC[A/C/G]ATCCACCCAAAGTCA | 67991 |
rs27201653 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26105015 | ACAGCCTGTGATAAA[C/T]GAACCAGTTCTTCAG | 67991 |
rs27201654 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26104798 | CCACCACAAAGGAAT[C/G]GAACCACAACAAAGA | 67991 |
rs27201655 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nacc2 | Mm_Celera | 2:26103914 | ATAAAGTAAACGACT[A/G]CAGAAGGACTGAGGG | 67991 |
rs27201656 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26103109 | AAAAAATGTGCAAAG[C/G]CACAAATGTCCAATA | 67991 |
rs27201657 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26102262 | CCCAGATTGAACAAT[A/C]ACAGACTGAACAAGT | 67991 |
rs27201658 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Nacc2 | Mm_Celera | 2:26102248 | GGCTCCTACTGGCTC[A/C]CAGATTGAACAATCA | 67991 |
rs27201659 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26101416 | GCTGCCGAGACCATA[A/G]CTTACCTGCCTTTGT | 67991 |
rs27201660 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26101362 | AACGTAAAAAGCATG[A/G]CGTTCTCCTTTCTCT | 67991 |
rs27201661 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nacc2 | Mm_Celera | 2:26101350 | TTCTCAGACCCTAAC[A/G]TAAAAAGCATGACGT | 67991 |
rs27201662 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26100493 | ACGTCACCAAGGCCA[A/G]ATACCTGCCAGGGAC | 67991 |
rs27201663 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26099268 | GCACAGGGTTCAGGT[A/G]CCCACGACCTTACTT | 67991 |
rs27201664 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26098074 | GACCCCAGGTGCTTC[A/G]AGGGAGCTGGACACA | 67991 |
rs27201665 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26097556 | TCAGAAGGTTGGGAA[A/G]AATCAGCCCCACACT | 67991 |
rs27201666 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26097300 | GCAAAAGCCAGTAAC[A/G]ATTCTAACATCTGCA | 67991 |
rs27201667 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26097248 | TGGACCTTGTGGATT[A/G]ATATGGCCCAGGAGA | 67991 |
rs27201668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26097184 | CCAAGCATCACAATG[A/G]CAGATTTTGCTACTT | 67991 |
rs27201669 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26096477 | GGAGGCAAGCCAATT[C/T]AAAACATTGACTTGT | 67991 |
rs27201670 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26096390 | GCAGCAGCCACAGAA[C/T]CCTGTTCTAACTGTA | 67991 |
rs27201671 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26096370 | CCAGACCCAGGCCTG[G/T]GCCAGCAGCAGCCAC | 67991 |
rs27201672 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26096279 | CCCTAGCACTAGGCA[A/G]TTCTCCAACATGGTA | 67991 |
rs27201673 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26096218 | CACAAGAGAAGACTA[C/T]ATCTCAGGCTCCATA | 67991 |
rs27201674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26096173 | TGACTGGACCAGAGC[C/T]AGCATTGCATAGGAT | 67991 |
rs27201675 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26096074 | ATCAAAATCTCTAGC[C/T]TCCTAATTTTGACAT | 67991 |
rs27201676 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26095949 | TACTCACGGGAACTG[C/T]ATGTTTGCTTGTTTG | 67991 |
rs27201677 | snp | A/G | 0.32 | 0.24 | intron-variant | Nacc2 | Mm_Celera | 2:26095935 | GCTTCTTCCCACGAT[A/G]CTCACGGGAACTGCA | 67991 |
rs27201678 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26095578 | GGGGCTCGGTGAGAA[C/T]AGCAAAGAAACCCCC | 67991 |
rs27201679 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nacc2 | Mm_Celera | 2:26095272 | TGGTATCTATCTACA[C/T]AGTGATCACCAGCAA | 67991 |
rs27201680 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nacc2 | Mm_Celera | 2:26095194 | TCCTGTCTGGAATCC[A/G]ACAGGCACTGTTCCA | 67991 |
rs27201681 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nacc2 | Mm_Celera | 2:26094921 | GAAGGTACTAAAACT[A/G]TATCCAGACACAGAG | 67991 |
rs27201682 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26094852 | GTCCCTTGAAAGCAC[C/T]GAAGCCAATAGGTAG | 67991 |
rs27201683 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26094783 | GTATCTCCAGAATAA[A/G]AAATGGGTGAGGTCT | 67991 |
rs27201684 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26094699 | CCCCAAAGCCAAGCA[A/C]AAACCCTACTGCTAT | 67991 |
rs27201685 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nacc2 | Mm_Celera | 2:26094654 | AAAAATCTTCAGGGT[A/G]TACCCTACTTTGGGA | 67991 |
rs27201686 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26094596 | TGCCTTTGCTTACCC[C/T]GTCTATCCTCACAGT | 67991 |
rs27201687 | snp | A/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093846 | CGGTGTCGGTTGTAT[A/T]GTGGGGTTAGGGTGG | 67991 |
rs27201688 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093807 | TCCTGCCGGCATTGG[C/T]CATTTCCTATGGTCT | 67991 |
rs27201689 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093686 | CACAGGCAATCCCAA[C/T]CAAACAGAGGCTCTC | 67991 |
rs27201690 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093466 | CTTCTTTCCAGAAAT[C/T]GTACAGGTAGGACTC | 67991 |
rs27201691 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093260 | AAGGAGGTAATGAGA[A/G]CCCTCAGGGTGGCTG | 67991 |
rs27201692 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093229 | CCTCCAAGCCTTTGT[C/T]GTCCTTGCCTCCTTA | 67991 |
rs27201693 | snp | A/C | 0.401235 | 0.199068 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26093119 | TGGAGCCATCTGGCA[A/C]CTCCTTATTTACACA | 67991 |
rs27201694 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26092905 | GCTATTGGGCAGCCT[A/G]CCTCAGTTTCTCTCA | 67991 |
rs27201695 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26092686 | TTTATCGCCAGGCAG[A/G]CCCCTGTAAGGTTAA | 67991 |
rs27201696 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26092620 | CCAGAACGCTACCTC[C/T]ACCTCACTCCATCTT | 67991 |
rs27201697 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26092568 | GAGCCAAACACTCTG[C/T]TGGGCCACAGGCTCC | 67991 |
rs27201698 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Nacc2 | Mm_Celera | 2:26092464 | GATGGGGAATAGGAA[A/G]AAGGGTGCCAAAGGG | 67991 |
rs27201699 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime, intron-variant | Nacc2 | Mm_Celera | 2:26092361 | AGCTGGCAACGCATA[A/G]AACTTAACTCTTCCT | 67991 |
rs27201700 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26091415 | GTAGAAGGGTCTCAG[G/T]ACTAAGCCCGCCAGG | 67991 |
rs27201701 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Nacc2 | Mm_Celera | 2:26091217 | GGGTGGAAGGGCTCC[A/G]GGTACACTCTGTGTT | 67991 |
rs27201702 | snp | C/T | 0.5 | 0 | intron-variant | Nacc2 | Mm_Celera | 2:26091177 | CTTCCTCCACTCTTT[C/T]CTTGGGGACAGACCT | 67991 |
rs27201703 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nacc2 | Mm_Celera | 2:26090992 | CCCCAGAGCAGGGAG[A/G]GCTTTAGTTTCAGGT | 67991 |
rs27201704 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Nacc2 | Mm_Celera | 2:26090714 | GAGAACCCCTGTCAC[C/T]TACTGCGTTCACAGA | 67991 |
rs27201705 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26089532 | TTGCAAGGTGCCCTG[A/C/T]CGTTTGTTACCTGCA | 67991 |
rs27201706 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nacc2 | Mm_Celera | 2:26089216 | AGAAGCTATCTACCC[A/T]GACCCAGGAGGCCCA | 67991 |
rs27201707 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nacc2 | Mm_Celera | 2:26088766 | AACACACACGATACT[A/G]GATACACTTTGCCCT | 67991 |
rs27201708 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26087459 | TGGCAGCACATCAGG[G/T]TAGGAACACATCTCT | 67991 |
rs27201709 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nacc2 | Mm_Celera | 2:26087436 | ACATGTAGTTCCCAA[G/T]TGTCTGTTGGCAGCA | 67991 |
rs27201710 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Nacc2 | Mm_Celera | 2:26087301 | GGCTTGGAGAACAGC[C/G]GTTCCAGAATATATT | 67991 |
rs27201711 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26087030 | CCAGGTCCCACACTA[C/T]CCTACTGGGCCTGCT | 67991 |
rs27201712 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26086987 | GGAGCAGAACCAGAA[A/C]ACAACCAAGGCCCTT | 67991 |
rs27201713 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26086571 | ATGGGCAGAACCCAG[G/T]AGTGGGTATCCTCAG | 67991 |
rs27201714 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26086206 | TCTGTGCAGGTCTAG[A/T]CAGCCCAGCCAGCTC | 67991 |
rs27201715 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nacc2 | Mm_Celera | 2:26085618 | CTATGGACCAAGCTG[A/G]GCTCTGACTATATGT | 67991 |