SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3661524 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122987114 | GCAGGGCAGGGCCCA[C/G]GAAGGGAGAAAGGCA | 30841 |
rs3662132 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122987257 | TTGGGGGGCCTTCAA[A/G]CCTAAGGCCGTCAAG | 30841 |
rs3662174 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Kdm2b | GRCm38.p3 | 5:122987275 | TAAGGCCGTCAAGCC[A/G]ATGGTCCCAGGGATG | 30841 |
rs3662807 | snp | C/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Kdm2b, A930024E05Rik | GRCm38.p3 | 5:122987391 | CCCTCCCTGGGTCCC[C/T]CTTAGTCCAATAGTC | 30841 |
rs3669266 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122916036 | AACCATCTGTAACTC[C/T]GGTCCCCGGGAATGG | 30841 |
rs3669862 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kdm2b | GRCm38.p3 | 5:122916136 | CACACATAAAAAAGC[A/G]TATCATAGACCCTTC | 30841 |
rs3670451 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Kdm2b | GRCm38.p3 | 5:122916224 | CTGTACTGGGAGCCA[C/G]TTAGTCCCCGCCCAG | 30841 |
rs6164615 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b, Gm33118 | Mm_Celera | 5:122949062 | AGAGAGACACTCTGC[A/G]CACTCACCTTGCCAC | 30841 |
rs6165772 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Kdm2b, Gm33118 | Mm_Celera | 5:122949303 | AATTTCCTCCTCTAT[C/T]GAAGTGGAGTTTCCC | 30841 |
rs6193173 | snp | C/G | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122876519 | TGGCTTACAAACACA[C/G]TGGGTTTATATTCAA | 30841 |
rs6213635 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Kdm2b | GRCm38.p3 | 5:122931013 | AGCAGTACAGGTCTC[A/G]GGGCATGGTATGAGC | 30841 |
rs6214020 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Kdm2b | GRCm38.p3 | 5:122931067 | TGCTTTCTACCTATG[A/C]CTGTGATTCAACAGG | 30841 |
rs6382063 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122905795 | CTATAAATATTAACA[C/T]GTACTGgaagattta | 30841 |
rs6382465 | snp | A/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122905832 | tgcacagaatgcttt[A/T]aaaaaaattgattta | 30841 |
rs29505806 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Kdm2b | GRCm38.p3 | 5:122919244 | AAGAGCACCACTGGA[C/T]AGAGAAACAAGCTGA | 30841 |
rs29506466 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122970851 | TAAAGGCATTTCCCG[C/T]CAAACCAGACAATCC | 30841 |
rs29506652 | snp | A/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122933470 | GATGGTTTAGCGGGT[A/T]AAGGCACTTGCTGCC | 30841 |
rs29509984 | snp | C/T | 0.465374 | 0.126941 | upstream-variant-2KB, nc-transcript-variant | Kdm2b, A930024E05Rik | Mm_Celera | 5:122989970 | AGTACAGCCCTGAAA[C/T]AGAAGTTGGGCTTTT | 30841 |
rs29511459 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kdm2b | GRCm38.p3 | 5:122900835 | ATCTGATGCCCGCGA[A/G]TCCCAGAGGCCCCCA | 30841 |
rs29512068 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kdm2b, Gm33118 | GRCm38.p3 | 5:122940251 | TTTGGGAGGGATTTC[C/G]TAGCCAAGAAAGCGT | 30841 |
rs29521446 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Kdm2b | GRCm38.p3 | 5:122937854 | TTGGTGTTCTATCCG[G/T]TTCCCCAGAGGCCTG | 30841 |
rs29523522 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Kdm2b | GRCm38.p3 | 5:122919594 | AGGGATTAGTAAACT[C/G]TAGATTAGCTTGGTC | 30841 |
rs29524354 | snp | A/C | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122939614 | TGAAAGAATCCAGAT[A/C]TGAAAGGTCACATAT | 30841 |
rs29525600 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Kdm2b | Mm_Celera | 5:122874759 | TCTCTAATTGTTACA[C/T]GAGACTGAAACAACA | 30841 |
rs29526167 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Kdm2b | GRCm38.p3 | 5:122927315 | TTGGACAGTGGACTC[C/T]TAATTTAGAACTGAC | 30841 |
rs29526918 | snp | A/C | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | Mm_Celera | 5:122988967 | TTGGCGGAGGGGGAA[A/C]GGAGGGAAGACCAAA | 30841 |
rs29531690 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122984007 | GAAGAAACACACACC[C/T]ATCACAGAAAGAGAC | 30841 |
rs29538351 | snp | C/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122930661 | AGAGGGGCGTGTCCC[C/G]TCAGCTAGCAGCATT | 30841 |
rs29541068 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122933465 | GACATGATGGTTTAG[C/T]GGGTTAAGGCACTTG | 30841 |
rs29546900 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kdm2b | Mm_Celera | 5:122974982 | TAATCCCAGCACTCA[C/G]GAGGCAGAGGCAGGT | 30841 |
rs29552012 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kdm2b | GRCm38.p3 | 5:122976538 | CGAAGGGTTAAAAAA[A/G]AAAATTCTCAAACAA | 30841 |
rs29555131 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122936128 | GAGCACCCCCTAGCC[C/T]CAGGTACCCCTTCTA | 30841 |
rs29556332 | snp | A/T | 0.455 | 0.143091 | intron-variant | Kdm2b | GRCm38.p3 | 5:122984283 | TCCCGAAAGAGCAGC[A/T]TTTCTTCTCCAGTGG | 30841 |
rs29556619 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122973611 | ATATCTCTTTAGAGA[A/G]AACGCTAACACAGGC | 30841 |
rs29561773 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Kdm2b | GRCm38.p3 | 5:122920884 | GGCTGCTCTTCCAAT[A/G]GTCATGAGTTCAATT | 30841 |
rs29564017 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Kdm2b | GRCm38.p3 | 5:122933135 | CCAGGTCAGTGTGCC[C/T]ACACAGGTTGCTTAG | 30841 |
rs29564272 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, nc-transcript-variant | Kdm2b, A930024E05Rik | Mm_Celera | 5:122989634 | CATTACCTATGCTGG[C/T]GACCTAAATTCAAAG | 30841 |
rs29564323 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122962537 | TTAATCATTGCAACA[A/G]TAACCCTAGCTACAA | 30841 |
rs29567595 | snp | C/T | 0.495 | 0.0497494 | upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | GRCm38.p3 | 5:122990433 | CAGGTGACGCTAGCT[C/T]GGCGTACAAGCTAAA | 30841 |
rs29568025 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | Mm_Celera | 5:122990695 | GAATTTTTTTTTTTT[A/T]AAATTCCATCCATGC | 30841 |
rs29568280 | snp | A/C/T | 0.484429 | 0.0868505 | intron-variant, upstream-variant-2KB | Kdm2b | GRCm38.p3 | 5:122986739 | ATGTCTAAGAAAAAA[A/C/T]CCTCAGCCACACTGT | 30841 |
rs29569244 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Kdm2b | Mm_Celera | 5:122901902 | AAAGATAACCCTTCA[C/T]ACACTTCCCTCTACC | 30841 |
rs29569345 | snp | G/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122897118 | TGGTCCCACATAGGG[G/T]AAGGAAAAAAAGAAA | 30841 |
rs29570231 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kdm2b | GRCm38.p3 | 5:122902137 | TTTCTCTGTCATTTG[A/C]CATACCTGCAAGGAC | 30841 |
rs29576936 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122935341 | AGGAAGGCCAGGAGG[A/G]GAAGATCACTTCCAA | 30841 |
rs29578825 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Kdm2b | GRCm38.p3 | 5:122878358 | CATTAATGTTAGCAC[C/T]GGTTCCTTTCTAGAG | 30841 |
rs29578967 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Kdm2b | GRCm38.p3 | 5:122969908 | ACCAGGTGACAAGGA[A/C]AGGCTGCCCCTGGAA | 30841 |
rs29628200 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Kdm2b | GRCm38.p3 | 5:122872693 | CCTGTGAATTATCAG[C/T]CCGGCAACCAGGCCA | 30841 |
rs29628675 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122973284 | CCTTCAGATACTCAC[A/G]GAGCCTGTACCCTCA | 30841 |
rs29630121 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | GRCm38.p3 | 5:122990189 | ATATTGTTTCTCAGC[A/G]GAGAAGGGGGGCAGC | 30841 |
rs29631929 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122933018 | GCTCTGTAGATCCCA[C/T]TCACTTTTATGCAAA | 30841 |
rs29634030 | snp | A/G | 0.475309 | 0.108333 | upstream-variant-2KB, nc-transcript-variant | Kdm2b, A930024E05Rik | Mm_Celera | 5:122989996 | CTTTTAAAGAGAAAG[A/G]AAAAAAAGTCTCTAC | 30841 |
rs29634685 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122978547 | TGTATAAGTGTGTGT[A/G]TGTGTGAATGTGTGT | 30841 |
rs29635415 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kdm2b | GRCm38.p3 | 5:122881132 | TACACCCCCACCACA[C/T]CGCAAGCCCAGTCTC | 30841 |
rs29674637 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122902817 | CAACTTGGTCTTACA[C/G/T]GTATGGAGTTCTCGG | 30841 |
rs29675713 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | GRCm38.p3 | 5:122990557 | GGTTCAGACAGATAC[A/G]GGGAGGAAGTGGCCT | 30841 |
rs29677889 | snp | G/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122931066 | CTGCTTTCTACCTAT[G/T]CCTGTGATTCAACAG | 30841 |
rs29678251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122980166 | AAAAGAAACACAAGC[C/T]GGGCGGTGGTGGTGC | 30841 |
rs29679183 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Kdm2b | GRCm38.p3 | 5:122958659 | CAAGGGACCGGTCAT[G/T]ATATACTTCTTCCTT | 30841 |
rs29681021 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122921566 | ATTGCAAGCTCAGCC[A/G]GGCAGTTGGTGGTGC | 30841 |
rs29682105 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122924428 | GCTGCAAGCCAGGAC[A/G]TTTGTCTCTCTGACT | 30841 |
rs29683948 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122920547 | TTGAGTGCTTGGAGT[A/G]TGTATGACAAGGAGC | 30841 |
rs29684173 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Kdm2b | GRCm38.p3 | 5:122928275 | AATACATTTAATCAA[G/T]TTGACCTGAGTTTCC | 30841 |
rs29716191 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Kdm2b | GRCm38.p3 | 5:122930573 | CCACATGGCAAGCAG[C/T]TGAGAACCTAAGTCA | 30841 |
rs29720179 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122980575 | GGAGGTGGGGCCCAC[A/G]GGAAGGTATTTAGGG | 30841 |
rs29726617 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kdm2b | Mm_Celera | 5:122875054 | AACAACAAAAAAATA[A/T]TGTAAAAAATGGTAC | 30841 |
rs29727756 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Kdm2b | GRCm38.p3 | 5:122969474 | GGACTACATTCCTGG[A/G]ATTTCCCTTGGAAAA | 30841 |
rs29729368 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122909352 | ATGACCAACTAATTA[C/G]AAAGAAGAAGAAAGA | 30841 |
rs29731390 | snp | C/T | 0.465374 | 0.126941 | intron-variant, upstream-variant-2KB | Kdm2b | GRCm38.p3 | 5:122953665 | CTTGGGAATGAGCAC[C/T]GGTCGTTGGGGAGGA | 30841 |
rs29731496 | snp | A/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122924176 | ATGAACAAGGTCTCC[A/T]GCAAGCTCGTGCACG | 30841 |
rs29732892 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Kdm2b, A930024E05Rik | GRCm38.p3 | 5:122991066 | TCAGTCACGCTGCTT[A/G]CCCTTTCAAATGTCC | 30841 |
rs29733400 | snp | C/T | 0.455 | 0.143091 | intron-variant | Kdm2b | GRCm38.p3 | 5:122957337 | GGACCGTTCCCTATT[C/T]CCAGAGGACTCCGTC | 30841 |
rs29736726 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kdm2b, Gm33118 | GRCm38.p3 | 5:122940295 | AGTGAGGATGGGCAC[G/T]GGGAAGCCGTGGCCC | 30841 |
rs29767923 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Kdm2b | GRCm38.p3 | 5:122976909 | ATACCTAACCAAAAC[C/T]GCCATGTTAATTATG | 30841 |
rs29774802 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Kdm2b | GRCm38.p3 | 5:122987009 | TTCGGACTGTCAAGG[C/T]TGTAGAAAGCGCTAG | 30841 |
rs29776819 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122917908 | TTTAAGGCCAGCCTG[A/G]TCTACAGAGCAAGTT | 30841 |
rs29779694 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Kdm2b | GRCm38.p3 | 5:122962564 | ACAACATGGTGCCAT[C/G]TCAGTATCCCCGAAC | 30841 |
rs29780565 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122903790 | CAGACTTAGCCTTAT[C/T]CCAGGGTGGGGAAAA | 30841 |
rs29780572 | snp | C/T | 0.401235 | 0.199068 | intron-variant, utr-variant-5-prime | Kdm2b, Gm33118 | GRCm38.p3 | 5:122950671 | GCCTTTTGCACCTCT[C/T]GTTCAGGTGGACCCG | 30841 |
rs29780658 | snp | C/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122910600 | CAGTCTGTCCATCAC[C/G]ACCTTAGTAGGAGAC | 30841 |
rs29820225 | snp | A/T | 0.5 | 0 | intron-variant | Kdm2b, Gm33118 | GRCm38.p3 | 5:122945564 | AGAGGCAAGAGGAGC[A/T]GGAGTTGGAAGACCT | 30841 |
rs29820509 | snp | C/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122930483 | GCCTCCCCAGTGTTG[C/G]GAAATTTCATTTCAT | 30841 |
rs29820554 | snp | A/T | 0.586667 | 0.142361 | intron-variant | Kdm2b, Gm33118 | GRCm38.p3 | 5:122948082 | TGCCTTTGGGGTATC[A/T]CGGTTCCGGGTGAAA | 30841 |
rs29821420 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122968765 | AAGAGGAGGGGTACA[C/T]AGTATCAGCATCAGA | 30841 |
rs29822637 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b, Gm33118 | GRCm38.p3 | 5:122946749 | GGATGAAAGGCGTGT[A/G]CCACCACTGCCCGGC | 30841 |
rs29823094 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122931143 | AAGAAGAGGAAAGGA[A/G]TTCGCTCTTCTACCT | 30841 |
rs33044860 | snp | A/G | 0.497778 | 0.0332592 | synonymous-codon | Kdm2b | GRCm38.p3 | 5:122880589 | CGTCTTTTGGATCTC[A/G]TGGTTGAGCTCCTTG | 30841 |
rs33050166 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122969237 | TATAAGGCACACCCC[A/G]GAATGCACCTTGGAT | 30841 |
rs33074787 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kdm2b | GRCm38.p3 | 5:122924132 | ACGGCTAGTTATAAA[A/G]TATCTTTGTCGACTA | 30841 |
rs33078747 | snp | A/G/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122977146 | CCTTGCATACCTGTG[A/G/T]TAGCCTGGCTGAAAG | 30841 |
rs33084191 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122977421 | TACACAATAAATACT[A/G]TGGACTGCCTAAGTA | 30841 |
rs33088180 | snp | C/T | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122976288 | TTTAATCCCAGCAGT[C/T]GGGAGGCAGAGGGAG | 30841 |
rs33090533 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122979801 | GTGGTTGAGTCCAGG[A/C]TGGTCTACAGAGTTC | 30841 |
rs33098745 | snp | G/T | 0.5 | 0 | intron-variant | Kdm2b | GRCm38.p3 | 5:122908843 | GTCCTAGAACTCACT[G/T]TGTAGACCAGGCTGG | 30841 |
rs33108847 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Kdm2b | Mm_Celera | 5:122920206 | ATACAAGAAAAAAAA[A/T]AGGTCAAAAAATTGG | 30841 |
rs33115239 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122931168 | CTACCTAGACAGAAA[C/T]CTGGCCTGGAGCCAG | 30841 |
rs33116800 | snp | A/G | 0.5 | 0 | intron-variant | Kdm2b | Mm_Celera | 5:122983489 | AATAAATAAGTACAG[A/G]CAGAGCCAGACAAGG | 30841 |
rs33117268 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm2b | GRCm38.p3 | 5:122980659 | TACCACCATATCAAG[C/T]TGTGATATGGTAAGA | 30841 |
rs33132598 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm2b | GRCm38.p3 | 5:122979870 | CATCTACAATCTCAA[C/T]GTGGAAGCCAGAACA | 30841 |
rs33136237 | snp | C/T | 0.486111 | 0.0821678 | intron-variant, upstream-variant-2KB | Kdm2b, Gm33118 | GRCm38.p3 | 5:122942027 | TTTAGTCAACAACAT[C/T]ATACCTCCATTTGAG | 30841 |