SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4165287 | snp | A/T | 0.474506 | 0.109987 | intron-variant | Senp2 | GRCm38.p3 | 16:22028847 | TCTTGAGCATAGGAA[A/T]GATGAATGAAGGCTG | 75826 |
rs4231130 | snp | A/C | 0.277778 | 0.248452 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047467 | AGTAACTGTGAGCAT[A/C]CATGTTAAGTCGTAG | 75826 |
rs4231131 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047471 | ACTGTGAGCATCCAT[A/G]TTAAGTCGTAGGTCT | 75826 |
rs6202629 | snp | A/G | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | Senp2 | Mm_Celera | 16:22009554 | gcagcggcagcggcg[A/G]cggcggcggcggcgg | 75826 |
rs6390664 | snp | A/C | 0.290657 | 0.246672 | synonymous-codon, nc-transcript-variant | Senp2 | GRCm38.p3 | 16:22038623 | GTTGCGAATCACCCG[A/C]GGAGACATCCAGACC | 75826 |
rs6404416 | snp | C/T | 0.5 | 0 | intron-variant | Senp2 | Mm_Celera | 16:22038770 | TTCTGTTTTGTTGCC[C/T]tttcttttagtgctg | 75826 |
rs6404519 | snp | G/T | 0.5 | 0 | intron-variant | Senp2 | Mm_Celera | 16:22038824 | cgttcaacaagcagg[G/T]gctctctctgctctg | 75826 |
rs6405476 | snp | C/G | 0.5 | 0 | intron-variant | Senp2 | Mm_Celera | 16:22038967 | acctctgttgtgatc[C/G]tcctgcctcactcac | 75826 |
rs6406098 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Senp2 | Mm_Celera | 16:22039085 | TTGACCTGAAGACCT[G/T]GTGCAAGCACTGTCC | 75826 |
rs6406127 | snp | A/G | 0.5 | 0 | intron-variant | Senp2 | Mm_Celera | 16:22039107 | GCACTGTCCCTGTGA[A/G]TTGTNCATCCCCTAC | 75826 |
rs6406136 | snp | G/T | 0.5 | 0 | intron-variant | Senp2 | Mm_Celera | 16:22039112 | GTCCCTGTGANTTGT[G/T]CATCCCCTACTAGTA | 75826 |
rs45638750 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22042060 | GAGAATTAAATTTTT[C/T]TTGAAAAACAAGCAA | 75826 |
rs45646820 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22024779 | AGGAGACAGGGCTTC[A/G]TTCTCTCTTGAGATC | 75826 |
rs45656129 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Senp2 | Mm_Celera | 16:22043593 | TTTTGAAATGTCAAC[A/G]GTATTTTTTTTTAAT | 75826 |
rs45676775 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22023516 | AATGCTTGTATGTCT[A/G]ACATTGCAAATGGTG | 75826 |
rs45779689 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Senp2 | Mm_Celera | 16:22042915 | TTTTTAATCACAGTG[A/G]GTGTTCTCTTGGGAC | 75826 |
rs45789946 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Senp2 | Mm_Celera | 16:22044908 | CTCCCTGCCGAGTTC[A/C]TATCTTCCCAGTCTC | 75826 |
rs45860623 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22044517 | GGATAACTTGCTTGT[C/T]CTTCAACTTCATTTG | 75826 |
rs46099764 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22024461 | CTAGACGCTGAGTGT[C/T]AGATGCCAGGTCCAC | 75826 |
rs46129718 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22041513 | GTCCTCAGGTCTTTC[A/G]GGATAAGGCACAGCC | 75826 |
rs46212950 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22024422 | ACTCACCGTACCTAC[G/T]GTTGCTGTGCAGACC | 75826 |
rs46228369 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon, nc-transcript-variant | Senp2 | Mm_Celera | 16:22040580 | ATGGACCAAAGGGGT[A/G]AATCTCTTCGAACAA | 75826 |
rs46228454 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22025973 | ACAGATTGAGGACTT[C/T]GGGTCTAACAGATAG | 75826 |
rs46284121 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22037485 | CTCTAATGCTTACAG[C/T]CACTGCACATGAAGT | 75826 |
rs46312612 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047451 | TTGAAACTGGATTCA[A/T]AGTAACTGTGAGCAT | 75826 |
rs46323933 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22030614 | CACCTCACCAACCCA[G/T]TGTGTTGGTTTCAAA | 75826 |
rs46441272 | snp | C/G | | | intron-variant | Senp2 | Mm_Celera | 16:22036108 | GGACAGCTGCTAAAT[C/G]TCATAGTCATTGTCT | 75826 |
rs46489689 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Senp2 | Mm_Celera | 16:22037600 | TCCAGGTGTGAGTTT[G/T]TATGTTCCAGCTGGG | 75826 |
rs46549901 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22028112 | TGCCCATAGTTTATG[A/T]GAGAGCACGCTACTG | 75826 |
rs46645192 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22036200 | ACATCACACACCAAA[A/G]CTGACTAGACCCTAA | 75826 |
rs46773042 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047469 | TAACTGTGAGCATCC[A/G]TGTTAAGTCGTAGGT | 75826 |
rs46776380 | snp | G/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048737 | AGGATTGACTTTTAG[G/T]CTCAGCCAGGTGTGT | 75826 |
rs46823015 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22022209 | TAAAATGGAAATCTG[C/T]GTGGCCTTAGGGTTG | 75826 |
rs46893501 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22027831 | AGAATGAATTGTTAT[C/T]TGGGAATTTTAACTT | 75826 |
rs46904848 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22045839 | ACTGAGCCATAGTTT[C/T]CTGCTTTAAGGTCAC | 75826 |
rs46959040 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22030911 | ACACAGATTTTACAT[A/G]GATACTGAACCAAAC | 75826 |
rs46986932 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22032904 | GGAACTACCAGGCAG[C/T]CAGAAAGAATGAAGA | 75826 |
rs47087766 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Senp2 | Mm_Celera | 16:22045927 | TTTCCTGTTGTGCCA[C/T]TGTGTGGACATTTCT | 75826 |
rs47106140 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22046622 | GTGTATAACACTGTC[A/G]TTCCTTTCAGCACCA | 75826 |
rs47173309 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22020745 | ATAAATCTTAAATAT[A/T]GCCTGATAAATCTTA | 75826 |
rs47202733 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22044409 | ACTGTTGCTGAGAAC[C/T]GTGGGTAAGGCCCCC | 75826 |
rs47267389 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22036307 | TGTCACTATCCAGTA[A/T]ATCTTTATGCACGTA | 75826 |
rs47279778 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22044370 | GCAGTGCCTGGCACA[C/T]TTCAGGCTCTTCAAA | 75826 |
rs47322924 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Senp2 | Mm_Celera | 16:22032116 | CAGGTATTCAAAAGG[A/G]AAAGCTGATACAGAG | 75826 |
rs47338346 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp2 | Mm_Celera | 16:22028643 | AATTAAGTTTTCTCA[C/T]TTTGCAAATTACATT | 75826 |
rs47373639 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22021842 | TGTCTTTATTAAAAC[A/T]TCTGGGCCTGGAAAA | 75826 |
rs47501422 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22039777 | TGATAACTATAAACA[G/T]TCGCTCCATTTGTTA | 75826 |
rs47612086 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22038712 | TCGGTCTGCTTAGTG[C/T]CTGTGGTCAGTGAGC | 75826 |
rs47619865 | snp | C/T | 0.32 | 0.24 | missense, nc-transcript-variant | Senp2 | Mm_Celera | 16:22028573 | AGAGGACCTCTCTGT[C/T]CAATGAGAAGTGAAA | 75826 |
rs47631347 | snp | C/G | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047488 | TAAGTCGTAGGTCTG[C/G]TGAGTGAGTGTGTGA | 75826 |
rs47650699 | snp | A/T | 0.336735 | 0.234472 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047042 | CACACGAATTCACTC[A/T]CTCATTGGGCAGTGC | 75826 |
rs47716972 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22044941 | AGAACTCACTACTGA[G/T]GAGTCTCCGCTCTTT | 75826 |
rs47725649 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Senp2 | Mm_Celera | 16:22037394 | TAAAATTCCTAGTTT[A/T]AAAGGGACTTTTCAT | 75826 |
rs47729457 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22030888 | ACATTGTACACATGA[A/G]CCCTTGCACACAGAT | 75826 |
rs47805037 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22025104 | TTATAAATGTGTTTG[C/T]CAATTGAGAATATCA | 75826 |
rs47837069 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22043309 | GGGCGATGCAGGCTG[C/G]GCACACAGCTTAGTC | 75826 |
rs47861927 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Senp2 | Mm_Celera | 16:22027748 | ACGTGATTGCAAAGA[A/C]GCAGAGTCTCATAAG | 75826 |
rs47929312 | snp | A/T | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Senp2 | Mm_Celera | 16:22026686 | AAAGTTATTGGAGCG[A/T]CTTAAAGAAGGTGCT | 75826 |
rs47957043 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048627 | CAGGTGAGTGATGCT[A/G]TAGCTAATGTGGCAT | 75826 |
rs48028331 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048598 | GTCCTGCTTGGATGG[C/T]GACTTTCTCTCCCCA | 75826 |
rs48113589 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22018459 | TCTTCTGTAAGTGAA[A/G]CTCACTGTTGTTAGG | 75826 |
rs48182043 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22022835 | AACACCAATATCGGG[A/G]CATGGGTGTATACTG | 75826 |
rs48222866 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22022160 | GAACACATGCAAATG[C/T]AAATCTAGCAATCCT | 75826 |
rs48268071 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22042898 | TAAATATCACAAAGT[C/T]CTTTTTAATCACAGT | 75826 |
rs48293144 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Senp2 | Mm_Celera | 16:22029548 | TGGGCCTTGCATTTG[A/C]GGTTCTGTGGACAGT | 75826 |
rs48298761 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22017530 | ACCTCATTACAGACT[A/T]GCAAGCCAAGAGAAG | 75826 |
rs48392202 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22028770 | TGTCTCTCATCCCTC[A/G]GTTATAAGGGCTTGT | 75826 |
rs48406014 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22044432 | AGGCCCCCAGTTGTC[A/G]GAAGCAGTGTCCTGC | 75826 |
rs48414573 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048851 | GAGCAGGAAGAGTGA[C/T]GGAGAACAACTTCCC | 75826 |
rs48446137 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp2 | Mm_Celera | 16:22021049 | CTTCTATTGCCTTGT[C/T]CCTCTTAAAACCCTG | 75826 |
rs48472594 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048959 | CAAAAGTACAGAATG[C/T]TAAGCTATGGTGGCA | 75826 |
rs48506131 | snp | A/C/G | 0.260355 | 0.249785 | intron-variant | Senp2 | GRCm38.p3 | 16:22021019 | CGTGGCATCTAACTC[A/C/G]ATAGTCTTTTGTCTC | 75826 |
rs48527900 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22045240 | ATAGGGCAAATATGC[A/G]AACCTCAATTTTGAA | 75826 |
rs48548266 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22048388 | AGAATTTATGATCCC[A/G]GCCTATCAAACAAAA | 75826 |
rs48612674 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22041612 | CAAGGAGTCTTGGCC[C/T]GTAATCCTGATGCCA | 75826 |
rs48642634 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Senp2 | Mm_Celera | 16:22026725 | CACGTTCCCTCCCAC[A/G]GTTTCACACCACAGG | 75826 |
rs48652861 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22049133 | AGTGAGTCGGCAAAA[C/T]TAAAGCCGGTAATGT | 75826 |
rs48680619 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22023454 | CTGGCTATGAGGACA[A/C]CTTTCATATGACAGC | 75826 |
rs48699715 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Senp2 | Mm_Celera | 16:22033303 | AAGTAGATTCCTCTG[G/T]GTGATGCTCTGTAGC | 75826 |
rs48740130 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Senp2 | Mm_Celera | 16:22044827 | TTTGATAGTTCCTGA[C/T]TGTCAGACAAGCTGC | 75826 |
rs48939869 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Senp2 | Mm_Celera | 16:22040928 | CAAAAGCTACAAGGC[A/G]CACTTTGAGGAAGAG | 75826 |
rs49004538 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22037842 | CATGTCAGGTAGAGA[C/G]ATGAAGCCATAAGAT | 75826 |
rs49012672 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22025004 | AGTGGGCCAGAGGCT[A/G]AGAGTTTTAAGAAGA | 75826 |
rs49023629 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22047432 | GAAGTAGCTTGGCTT[A/C]CTCTTGAAACTGGAT | 75826 |
rs49032562 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22022726 | AGGAGAACTGAAAGA[C/T]TCGTGAAACTCCAGC | 75826 |
rs49050073 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22030948 | TTTTGCCAACTCATA[C/T]ACCTCCTCAGCTCCC | 75826 |
rs49064307 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22040275 | TGAGGGGCTCAGGCC[A/G]TGGCCCTTCATCCTT | 75826 |
rs49091920 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Senp2 | Mm_Celera | 16:22043257 | TGGAGTAAGCCTTCC[G/T]CTATTCTCCTTCTCA | 75826 |
rs49194936 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Senp2 | Mm_Celera | 16:22020843 | GCATTTAGTAAATAT[A/G]TGTGTAAAAGTTCCA | 75826 |
rs49210615 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22033019 | CAACTTTGTATCTGT[A/G]GGCAAGTGCTCCATT | 75826 |
rs49336430 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22036723 | TTGCTTTGAGAAATT[C/T]CTCCAGATAAGGAAT | 75826 |
rs49425532 | snp | A/C/G | 0.336735 | 0.234472 | intron-variant | Senp2 | GRCm38.p3 | 16:22018487 | AGGTGATTTCACTGC[A/C/G]TTCTGTTACATAATC | 75826 |
rs49425668 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Senp2 | Mm_Celera | 16:22041056 | TTAGAGCATGTTCTA[G/T]TAATCTCACATCACT | 75826 |
rs49433138 | snp | A/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22039654 | ATCTCCAGAGGATCT[A/T]ATGCCTCCACTCAAA | 75826 |
rs49436449 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Senp2 | Mm_Celera | 16:22018512 | ATAATCTGAGGGTAC[G/T]AGCTGGTAGCATGTG | 75826 |
rs49520146 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp2 | Mm_Celera | 16:22044473 | GCAGCGTGTATTCTC[A/G]GGACTGCCCTGCTCT | 75826 |
rs49678157 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp2 | Mm_Celera | 16:22043939 | TCCTCTTATCTCAGC[C/T]CTCGCCGTGTGTGCT | 75826 |
rs49678578 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Senp2 | Mm_Celera | 16:22046842 | GAAGGCCTCTCCACA[A/G]TGGCCCTGACTAGAG | 75826 |
rs49829993 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Senp2 | Mm_Celera | 16:22026497 | TTTAAAGAAGTATAA[A/G]ACTAGAATTTGACTA | 75826 |
rs49862165 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Senp2 | Mm_Celera | 16:22024268 | ACCCTGTTAGCCTGA[A/T]ATCTTAAAGAAATGT | 75826 |