SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6245816 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316325 | CTACAGGACATCATG[C/T]GTAGAAGGACAGGGA | 69149 |
rs6342525 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316172 | attcaaaccactata[A/G]CCATAAAGTGGCTAA | 69149 |
rs6343053 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316267 | TTAAAGGTAGAAGAT[A/T]TGTAGTATGTACATC | 69149 |
rs13473166 | snp | A/G | | | upstream-variant-2KB, missense, utr-variant-5-prime | Kbtbd3, Aasdhppt | Mm_Celera | 9:4309342 | TGCCAAGTCGAGCCG[A/G]ATGGCTTCTGGCGAT | 69149 |
rs30512872 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kbtbd3 | GRCm38.p3 | 9:4322375 | CAATGGAGTTCTACT[C/T]ACCCATTAAAAACAA | 69149 |
rs30648757 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Kbtbd3, Aasdhppt | GRCm38.p3 | 9:4308273 | ATGAATTTTTAAGAA[A/G]CCTTTTTGAAGCACA | 69149 |
rs30859083 | snp | C/T | 0.277778 | 0.248452 | synonymous-codon | Kbtbd3 | GRCm38.p3 | 9:4330518 | TCCATTTTCCTCAGT[C/T]TTATGGATGAATATA | 69149 |
rs31342447 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Kbtbd3 | GRCm38.p3 | 9:4312162 | AGTAGGCTTCAGTGC[C/T]AATTAAGGAACAGAT | 69149 |
rs31566009 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Kbtbd3 | GRCm38.p3 | 9:4319151 | TTCTGTGCTTGCTTA[A/G]CATCCTGTTGCTTAT | 69149 |
rs31718188 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316811 | CTAGAATAAAAAAAA[A/T]AGTGTGATAGGAAGC | 69149 |
rs45934203 | snp | C/G | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314472 | CTTATTTTATGCTGC[C/G]AGGCTTTTGTCTTAA | 69149 |
rs45966461 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319618 | TCTCCTGGCCAATAA[A/C]GACACGGGTATCTTT | 69149 |
rs46027536 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Kbtbd3, Aasdhppt | Mm_Celera | 9:4310875 | CTAAGAATCCTGTTA[C/T]AGTGTCTTTCCCCGT | 69149 |
rs46311806 | snp | A/C/T | 0.165289 | 0.235211 | intron-variant | Kbtbd3 | GRCm38.p3 | 9:4321006 | TTAGTAAATAATACA[A/C/T]AACAAAATGTAGCTT | 69149 |
rs46345208 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316678 | AGATGGATGTCAGAA[A/G]ATAGTTTGGTGGAGT | 69149 |
rs46400514 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318328 | ATGAGCAATGAGGCC[A/T]CTAACGACAATCGTA | 69149 |
rs46429019 | snp | A/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318022 | GGTGAACTTGATCTT[A/T]TGAAGGAAGGCATTA | 69149 |
rs46479605 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318116 | AAATTATTGAAGCAG[C/T]CACACGGTTTCTAAA | 69149 |
rs46648870 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318121 | ATTGAAGCAGTCACA[C/T]GGTTTCTAAAATATT | 69149 |
rs46660036 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4317239 | TGAATAGGGAATCTT[A/C]TCATTTTTTGACCAT | 69149 |
rs46704665 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Kbtbd3 | Mm_Celera | 9:4312150 | CCACTAGATCATATC[C/T]GTTCCTTAATTGGCA | 69149 |
rs46706198 | snp | G/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314202 | GCAGCATGTACTGAG[G/T]ATGAGCAAACATACT | 69149 |
rs46755376 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB, utr-variant-5-prime | Kbtbd3, Aasdhppt | Mm_Celera | 9:4309482 | CAGGTAGAGCAGACG[A/C]TGACGTAGCCACGCC | 69149 |
rs46870680 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Kbtbd3 | Mm_Celera | 9:4331349 | CAGTAGTAGGTCAGA[A/G]TGGGAAGAGGTGTCA | 69149 |
rs46996422 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318652 | CTGTGGAGGTGCCAC[A/T]GTTAGAGGCTGAGCA | 69149 |
rs47212323 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319540 | GAAAGGGAGATTGCC[A/C]TGATGATAGTAGGTT | 69149 |
rs47272697 | snp | A/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318390 | TTTACAAGTAAAAGT[A/T]CACATAGATCATTAC | 69149 |
rs47296874 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4317666 | CATGAAGGAATTTGC[C/T]TACTATGGAAGCAAA | 69149 |
rs47356922 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316634 | ATGAGTACATTTTTT[A/T]AAAAATTCATTATGG | 69149 |
rs47411191 | snp | A/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Kbtbd3, Aasdhppt | Mm_Celera | 9:4310546 | TTCCTAGAGATGGGT[A/T]TAGTCTGATCTGTAC | 69149 |
rs47568794 | snp | A/C | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319063 | TACTACAAATGCAAA[A/C]TGAAACAAAGATTTG | 69149 |
rs47720126 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kbtbd3 | Mm_Celera | 9:4329205 | CTGAGTTCAAGATAG[C/T]ACCAATCCTTTAGAT | 69149 |
rs47731458 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318884 | TCGGTAACTGGGCTG[C/T]AGGCTAGAGCAGAAA | 69149 |
rs47836153 | snp | G/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4327857 | ATCATTTATAATACC[G/T]ACAGTTTGAGAAAAC | 69149 |
rs47872139 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314435 | TGGGCCTGCATGTAG[A/G]AAGCAAAATGGCTAC | 69149 |
rs47971013 | snp | A/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4328817 | AACATGACCAAAACA[A/T]TTTATAAAAGAAACT | 69149 |
rs47985912 | snp | A/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314392 | TGTAACCTGTCCTGA[A/T]CCAGCCTTGAACTTG | 69149 |
rs48067886 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Kbtbd3 | Mm_Celera | 9:4327643 | TATTAATTGGTTTGT[G/T]TTGCTTATATTCAAA | 69149 |
rs48121251 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318580 | ATCCTTGAATTTGAA[A/G]ATGCACCAGTGCACA | 69149 |
rs48362053 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Kbtbd3 | Mm_Celera | 9:4311643 | ACTGGAACATCAAAT[C/T]ACTGCCACATTAGAA | 69149 |
rs48403668 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319780 | TTAATATATGAAGCA[A/G]AATAGTAATTATATT | 69149 |
rs48519068 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314112 | TCTGCCAGTTAAAAA[A/T]CTCAAGCACAGCAGG | 69149 |
rs48570007 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kbtbd3 | Mm_Celera | 9:4320786 | CAGCATGATTTTCTT[A/G]CAATGTTTTCTAGCT | 69149 |
rs48810827 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318852 | GAGGTGCTGAAGATG[C/T]GTCACATTTCACAGA | 69149 |
rs48860269 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318898 | GTAGGCTAGAGCAGA[A/G]ATGTTTTCTTTCTCT | 69149 |
rs48862204 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd3 | Mm_Celera | 9:4317236 | TTTTGAATAGGGAAT[C/T]TTCTCATTTTTTGAC | 69149 |
rs48872345 | snp | A/G | 0.42 | 0.183303 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319465 | AGGGGAGGAACTGCA[A/G]CCCAGAAGACTTTTT | 69149 |
rs48930662 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Kbtbd3 | Mm_Celera | 9:4330365 | GTTATCTGAGGACAC[A/G]CTTCAAGACTATTTG | 69149 |
rs49016121 | snp | A/C | 0.35503 | 0.226867 | upstream-variant-2KB, missense, intron-variant, utr-variant-5-prime | Kbtbd3, Aasdhppt | Mm_Celera | 9:4308803 | GAAATTGGGATATGG[A/C]TTCAACGAGTCTTTC | 69149 |
rs49033382 | snp | C/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4320902 | GTTAATTTTTTGATG[C/T]TAATTCTTTGGGTTT | 69149 |
rs49090038 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4317174 | ATGCTATAATAATGG[C/T]TAATTCTTAATAAAA | 69149 |
rs49195954 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4320211 | GCACAGCTTTCCTTC[C/T]ATGTAACTTTTAGAG | 69149 |
rs49212745 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4312591 | TTATAACAAGGATTT[A/G]TTGCTAAGCCTAATT | 69149 |
rs49236496 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-5-prime | Kbtbd3 | Mm_Celera | 9:4311515 | AACCCTCATGTCTAG[C/T]TATGCACTGTCCTGG | 69149 |
rs49247217 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318918 | TTTCTTTCTCTTATC[A/C]TAAATACTTCAGGTT | 69149 |
rs49414776 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Kbtbd3 | Mm_Celera | 9:4312109 | GTGTATGTATGTCTG[C/T]CATATTCTCCAAAAC | 69149 |
rs49625419 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Kbtbd3, Aasdhppt | Mm_Celera | 9:4310628 | AGCTACATGGCAGTT[C/T]GAGTCACTCACACAC | 69149 |
rs49656292 | snp | C/G | 0.297521 | 0.245442 | upstream-variant-2KB, intron-variant | Kbtbd3, Aasdhppt | Mm_Celera | 9:4309163 | TGAAGACGGTCGCAC[C/G]CACTCCGGAGGCTCC | 69149 |
rs49668635 | snp | A/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Kbtbd3, Aasdhppt | Mm_Celera | 9:4309117 | AGGGAAGACTAGATG[A/T]GAGTGACCCAGGCCT | 69149 |
rs49894175 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314373 | GATTGGCCAACAACT[A/G]TTGTGTAACCTGTCC | 69149 |
rs50213488 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4320854 | AATCTTCTGCTCTTA[C/T]CAAACTTACTTTTTA | 69149 |
rs50305080 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kbtbd3 | Mm_Celera | 9:4329687 | AAGTATTATACCATA[C/T]AGTTATTTTAAATGT | 69149 |
rs50310076 | snp | A/G | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319577 | GCGATGAGGTCAGAT[A/G]TATTATTACAATACT | 69149 |
rs50318599 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4327957 | AGATATAAAATCAAG[C/G]AACATGTCGTATAGA | 69149 |
rs50475948 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Kbtbd3, Aasdhppt | Mm_Celera | 9:4309571 | CACCCCTTTTCAGGC[G/T]TCTGTGCGAAGTAGC | 69149 |
rs50597793 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Kbtbd3 | Mm_Celera | 9:4331485 | AGCTCTAAAATTGCA[A/C]CTAGTAGAATTGGTT | 69149 |
rs50602748 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Kbtbd3 | Mm_Celera | 9:4330422 | CACAAACTGTTTTGA[C/T]ATAATCGTGGATGCC | 69149 |
rs50684476 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318949 | CACATACTATGTCTT[C/T]GTGTCAAAACTGGAA | 69149 |
rs50768586 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4327678 | AATAGGTACAAATGT[A/G]GCTAGAATTTTTTAA | 69149 |
rs50921125 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4314905 | CTACTTACTCTTCTA[A/G]GCCTGACCTTGCTGA | 69149 |
rs51022575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4315729 | TTTACAATACTTAGT[A/G]CCAGTATGCTGTTTT | 69149 |
rs51151208 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4315248 | AGAAAAGAACATTTA[A/T]GCAAACCATGTCCTT | 69149 |
rs51185887 | snp | C/T | 0.165289 | 0.235211 | downstream-variant-500B, utr-variant-3-prime | Kbtbd3 | Mm_Celera | 9:4331821 | AGTAGATGAGAAATT[C/T]ACATTGAACACTCTG | 69149 |
rs51438288 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4328057 | ATGTGTCTTCTGCAA[A/G]GGTGTAGAAGCTGAT | 69149 |
rs51611087 | snp | C/T | 0.297521 | 0.245442 | upstream-variant-2KB, intron-variant | Kbtbd3, Aasdhppt | Mm_Celera | 9:4307959 | CTTAATACTTTCCTA[C/T]TATTTAAAACGTCAA | 69149 |
rs51675450 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4320027 | GAGATCAGTGATTCA[C/T]AATGTCCTCGATCAG | 69149 |
rs51778115 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Kbtbd3 | Mm_Celera | 9:4319398 | GATACCATCTTAGCA[A/G]AAGGTGAAATGACAA | 69149 |
rs51788444 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kbtbd3 | Mm_Celera | 9:4312673 | TTTGAAGTCACTTCC[A/G]TGAATACATAGCATA | 69149 |
rs51837799 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Kbtbd3 | Mm_Celera | 9:4327976 | ATGTCGTATAGAAAC[C/T]GCTTATAATAACATG | 69149 |
rs51854007 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316762 | CTGATAAGTTATGTT[A/G]CCAGAGGTCAAATTA | 69149 |
rs51922355 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Kbtbd3 | Mm_Celera | 9:4318807 | TGTTATTATGCCAGG[A/C]CTTCAGTGCTGACCA | 69149 |
rs51997900 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kbtbd3 | Mm_Celera | 9:4316183 | TATAGCCATAAAGTG[A/G]CTAATACCACCAAAC | 69149 |
rs52049335 | snp | G/T | 0.32 | 0.24 | intron-variant | Kbtbd3 | Mm_Celera | 9:4317385 | GACTTCTTTTAGACA[G/T]CTCACATGGTCAAAG | 69149 |
rs52157797 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Kbtbd3 | Mm_Celera | 9:4313284 | GCCAGTAGGGTGGCT[A/T]TGGCCCAGGCTCTCT | 69149 |
rs52199016 | snp | G/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4313102 | TTTTTTTTTTTTTTT[G/T]GGTGCATAAGAGAGA | 69149 |
rs52204542 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kbtbd3 | Mm_Celera | 9:4313282 | TGGCCAGTAGGGTGG[C/T]TATGGCCCAGGCTCT | 69149 |
rs52264993 | snp | A/G | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4313234 | AGAGAGAGAGAGAGA[A/G]AGAAAGAGAGAGAGA | 69149 |
rs52428401 | snp | G/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4313105 | TTTTTTTTTTTTTGG[G/T]GCATAAGAGAGAAAA | 69149 |
rs52496892 | snp | G/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4313675 | GTTTTTATTTATTTG[G/T]TTGTTTATTCTATTT | 69149 |
rs108198577 | snp | C/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4322801 | TCAACTGAGAAATAT[C/T]AAATGGCTTAGAAGC | 69149 |
rs108236536 | snp | C/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4322766 | CCTGATGACTAAGGA[C/T]GTTGAACAGTTTTTT | 69149 |
rs108530585 | snp | A/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4312872 | AAATGCCTCTGGCAG[A/T]TCTCTCTCTCATATC | 69149 |
rs211791189 | snp | C/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4321436 | ACTATCTGCTGTGTA[C/T]ATTATGTCCATTAGA | 69149 |
rs211824102 | snp | A/G | | | intron-variant, upstream-variant-2KB | Kbtbd3, Aasdhppt | Mm_Celera | 9:4311158 | TGTCTAACAGAGAAG[A/G]AGAAATTTCTAATGT | 69149 |
rs211864361 | snp | A/G | | | intron-variant, utr-variant-5-prime | Kbtbd3 | Mm_Celera | 9:4312034 | AAGAGCATACAAAAT[A/G]TGCAGAAGTAGCAGC | 69149 |
rs212024592 | in-del | -/TC | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4329811 | TATAATTAAAATATT[-/TC]TGTTTACTTGTGCTT | 69149 |
rs212248624 | snp | C/T | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4322997 | CCTATTGACAGTGTC[C/T]TTTGCCTTACAAATG | 69149 |
rs212392946 | snp | A/C | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4313289 | TAGGGTGGCTATGGC[A/C]CAGGCTCTCTGATAA | 69149 |
rs212392965 | snp | A/G | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4324165 | AGCTATGGGCCTTGA[A/G]TTCCTGATCTTTTCA | 69149 |
rs212424535 | snp | A/G | | | intron-variant | Kbtbd3 | Mm_Celera | 9:4314187 | ATCGGCAGTTGAAGA[A/G]CAGCATGTACTGAGT | 69149 |